Vaccination: Pain, Profit, and Politics - Part 1 By Gary Null, Ph.D., and Martin Feldman, M.D.
February 8, 2013
Gary Null in Gary Null, Gary Null Vaccine, Myth of Vaccination, Vaccines, Vaccines, are vaccines safe?, flu vaccine, mandatory vaccination, sham vaccines, vaccine damage
Vaccination: Pain, Profit, and Politics - Part 1
By Gary Null, Ph.D., and Martin Feldman, M.D.
 Today we have a major controversy brewing in the U.S. healthcare field.  The 
question is being asked if the vaccinations that we are giving our children are safe 
and effective.  What is the proof that vaccinations are safe?  We have undertaken 
an enormous job of reviewing the world literature to examine whether vaccinations 
are safe, and whether they are effective. We have taken an in depth look at the 
politics, the economic incentives, and the conflicts of interest involved in the 
politics of vaccinations. We have reviewed the scientific literature and we have 
examined the results on the people who have received vaccinations and the health 
effects of these (often mandated) medical procedures.
 We have examined here the myths versus the facts in the science of vaccines, and 
whether the procedures themselves represent good science or whether the 
manufacturers and physicians who provide them support conjecture or good 
scientific practice.  We have examined the lobbying on behalf of the vaccine 
makers, and we have examined the safety and efficacy of the dozens of 
vaccinations that children are receiving in the first months of life.  Our society 
rarely looks at the safety and efficacy of medical manufactures which have 
enormous power to  influence the decisions of the CDC, the FDA, and the 
Institutes of Allergy and Infectious Disease
[1] [2] [3] [4] [5] [6] [7] [8] [9] [10]
, but the 
media rarely hears of the trajedies and the side effects.  We do, however, hear that 
vaccines promise to prevent some new condition, (such as genital warts.
[11] [12] [13]
)
 However, we have innundated the developing baby's body with dozens of 
vaccines
[14]
, but no industry advisor or anyone in the FDA has ever suggested that 
this is too much. We are overwhelming the child's system with adverse effects, and 
all this has happened in the last 40 years.
 Let us now examine the truth:
Life Expectancy in the 20
th
 Century When we take a look at the article by 
David R. Francis, entitled, "Why do Death Rates Decline"
[15]
, to get a general idea 
about how vaccinations might play a role in general health throughout the 20th 
century, we see that mortality rates decline steadily but rapidly throughout the 20th 
century.  Using this logic, vaccine advocates might wonder why increased rates of 
vaccination in the past two decades wouldn't have made mortality rates decrease 
faster than in the first half of the century. However, we learn that:  "During the twentieth century, mortality rates declined quite rapidly in the 
United States and in all developed countries. Except for a 10-year period between 
1955 and 1965 when the mortality rate was essentially flat, mortality rates have 
declined at the relatively constant rate of approximately 1 to 2 percent per year 
since 1900.
[16]
  If vaccines were the cause of the decline of disease, then shouldn't the rates 
of mortality have declined more rapidly in the latter half of the 20
th
 century, with 
the use of more and more required vaccinations?
 The second point that Francis makes is that in the second half of the 20th century, 
the most mortality decline occurred in people who were in mid- life.  Vaccine 
advocates might argue that mortality rates ought to have declined more quickly in 
very young and school aged children: 
 "In the latter four decades of the century, about two-thirds of life 
expectancy improvements resulted from mortality reductions for those over age 
45.
[17]
"
Thus, the most improvements in terms of mortality in the second half of the 
20
th
 century occurred in people beyond the age of childhood vaccinations.
 The third point that the author makes is self explanatory:  improved nutrition and 
public health measures in children were more important than medical intervention 
in 1900.  This was the height of the measles outbreak.  In addition, 
"Infectious diseases were the leading cause of death in 1900, accounting for 
32 percent of deaths. Pneumonia and influenza were the biggest killers. Therefore, 
improved nutrition and public health measures, particularly important for the 
young, were vastly more important in this period than medical interventions.
[18]
"
The fourth point Mr. Francis makes is that in the mid 20th century, 
penicillin, sulfa drugs, and antibiotics contributed to a mortality decline in 
children:  
"Between 1940 and 1960, infectious diseases as a cause of death continued 
to decline. But more of this decline was attributable to medical factors, such as the 
use of penicillin, sulfa drugs (discovered in 1935), and other antibiotics. These help 
the elderly as well as the young, thereby reducing mortality across the age 
spectrum. By 1960, 70 percent of infants could be expected to survive to age 
65.
[19]
"Vaccinations were not mentioned in this paragraph.
 The fifth important point of Mr. Francis is that smoking habits of Americans is an 
important factor in reducing mortality rates throughout the 20th century. The 
important issue to note here is that smokers generally begin their habit well after 
vaccination schedules have been completed, and that smoking causes a huge health 
risk despite vaccinations received:
"Smoking cessation and better diets also are factors in [mortality decrease]: 
per capita consumption of cigarettes rose from essentially zero in 1900 to more 
than 4,000 per year per capita in 1960, or over two packs per smoker per day. 
Since then, per capita consumption has fallen by more than 50 percent. These 
trends affect death from heart disease and from smoking-sensitive cancers with a 
10 to 20-year lag.
[20]
"
Trevor Gunn, a biochemist in England,  claims that immunity from 
vaccination is shorter lived than natural immunity provided by the illness itself.  
First, a child may contract an illness in adulthood for which it was vaccinated in 
childhood, and second, a mother may not be able to impart immunity provided by 
vaccination as easily as the immunity she developed over the course of her natural 
life. 
[21]
According to a leaflet by the CDC, figures of average morbidity by various 
illnesses were reduced as a result of vaccination according to the flyer 
entitled,"What would happen if we stopped vaccinations?
[22]
"  The leaflet, 
however, does not include information on the other public health measures that 
coalesced to provide increased public health in the 20th century as well.
A detailed review of morbidity and illness factors in Union Soldiers in the 
Civil war illustrates that the onset of what we think of now as 'old age' illnesses occurred in much younger men during the 19
th
 century, but improved throughout 
the 20
th
 century: 
"chronic illnesses affected young and middle aged men to a much 
greater degree in the past than today.  [In a study of two cohort groups 
of Union Soldiers] one quarter of men aged 20-24 and over half of 
men aged 35-39 were rejected as unfit to serve due to illnesses such as 
cardiovascular disease and hernias.  Similarly, elderly men were more 
likely to suffer from chronic conditions than in the past...Of men aged  
60-64 during the 1890-1910 period, 90% suffered from a chronic 
condition, as compared to 75% of same aged men in 1994.
[23]
"
For example, for two of the conditions studied that we know now to be 
related to inflammation
[24] [25] [26] [27]
and stress
[28]
 (particularly as results from 
diet
[29] [30] [31] [32] [33] [34] [35] [36] [37] [38]
and lifestyle
[39] [40] [41] [42] [43]
), that is, heart 
disease and arthritis, we see that the average age for onset for the 1830-1845
[44]
cohort was approximately 56 years of age, whereas the average age of onset for the 
1918-1927 cohort was approximately 66 years
[45]
, or a difference of 10 years in the 
age of onset in the later group.  Similarly, for the arthritis sample, the average age 
of onset for the 1830-1845 cohort was approximately 54 years whereas the later 
cohort was approximately 65 years
[46]
 .  
So we see that as time goes on, at least two public health markers were 
improved greatly in the 20
th
 century; the age of onset of chronic disease in the 
forms of heart disease and arthritis was increased considerably.  These health 
factors, too, were improved without the help of vaccinations.
[47] [48] [49] [50]
(We will 
discuss this assertion later in this paper)
For more than a hundred years, however, two basic assumptions have been 
put forth by public health officials. One is that vaccines are safe.
[51] [52]
The second 
is that vaccines are effective for the conditions for which they're given.
[53]
 The 
public and our legislators have, by and large, accepted these assumptions as true, 
and as a result it is now compulsory in many states that children have as many as 20 
[54] [55]
separate inoculations before entering school, or 33 by the time they are 
finished with secondary education. Some of these are given as early as the first few 
weeks of life.
[56]
We've been told that the end of polio, for example, as a serious health threat 
is due to mass inoculation programs
[57] [58]
, and again we have accepted the official 
dogma without question. But as we shall see, this is not exactly the truth.
[59]
 What's 
more, a disturbing reality that generally has gone unrecognized is the ever-growing 
number of people suffering adverse reactions to vaccinations
[60]
. These individuals 
are predominantly infants and children, and the problems they've incurred as a 
result of vaccination go far beyond sore arms and transitory fever: Conditions such 
as autism, attention deficit disorder, minimal brain dysfunction, and other 
biochemical and neurological abnormalities have been linked to the effects of 
vaccines
[61]
. Most tragically, so has SIDS-sudden infant death syndrome.
[62]
[63]
Although the government agencies such as the CDC
[64]
, the National Institutes 
of allergy and infectious disease 
[65] [66]
, among others
[67] [68] [69] [70]
, have tried to 
debunk a possible link between the proximity of vaccinations and untimely deaths 
of children in the first few months of life, we cite the government's involvement in 
supporting the cigarette industry in the first half of the 20
th
 century
[71] [72]
, and the 
widespread use of pesticide. The government also touted the benefits of hormone 
replacement therapy until 2002
[73] [74]
, for which women are now suffering breast 
cancer
[75] [76]
, stroke
[77]
, and dementia
[78]
; the government does not have a good 
track record on the issue of dangerous NSAIDS such as Vioxx
[79]
, for the use of 
which over 100,000 deaths are attributed
[80]
.  As a result, the fact that we do not 
accept the government data on this issue does not mean that we are slanted, but it 
means that we are careful to point out the differences between the data that is 
reported and what the government deems is true.  We examine the government's 
point of view on SIDS on page 18 of this paper.  
Because of underreporting of these troubling statistical links
[81] [82] [83]
,
however, a full picture of the effects of vaccination has not emerged. The problem 
of underreporting is a deep-seated one
[84]
. Yet the official line is that a small 
minority must accept negative consequences for the greater good of the majority.This investigation is an attempt to uncover the truth. In three parts, we will 
discuss facts that challenge our assumptions about vaccine safety and 
effectiveness, look at the effects associated with specific vaccines, and summarize 
some of the legal, political and economic issues surrounding the use of vaccines. 
The series has required a review of thousands of articles. We are presenting 
information based upon hard science; hundreds of references are included here for 
those who want to read further. For people challenging mandatory vaccination 
policies, the reference section will be particularly helpful.
Why We Should Question Our Assumptions
We think of vaccinations as panaceas and look to science to develop new 
ones for every known affliction, from the common cold to AIDS. Jamie Murphy, 
author of What Every Parent Should Know About Childhood Immunization,
[85]
attributes society's general acceptance of vaccinations, in large part, to state laws 
that dictate children must receive vaccines before they can attend school.
     
However, we must take a close look at our assumptions and ask, are we 
seeing the full picture? The reasons we should challenge our beliefs include the 
following:
Safety issues. Significant adverse effects have been reported with every type 
of vaccine 
[86] [87]
. These reactions can occur soon after vaccination (short-term 
reactions) or several months to years later (long-term)
[88]
. Delayed reactions are 
more insidious and less obviously linked to vaccination, and thus necessitate largescale epidemiological studies to be proven.
One would think that before injecting children worldwide with hundreds of 
millions of doses of vaccines, enough clinical trials would be performed to 
determine exactly what the effects of this large-scale human genetic experiment 
would be. Lack of funding is not the problem. Each year, more than $1 billion
[89][90]
 is appropriated by Congress to federal health agencies to develop, purchase, and 
promote the mass use of vaccines in the U.S. but not to fund independent 
researchers to investigate vaccine-related health problems.
In the meantime, as an example of the volume of adverse reactions reported 
to the Vaccine Adverse Event Reporting System (VAERS), there were 38,787 such 
events between 1991 and 1994. Of these, 45 percent occurred on the day of 
vaccination, 20 percent on the following day, and 93 percent within two weeks of 
vaccination. Deaths were most prevalent in children 1 to 3 months old and were 
defined as sudden infant deaths. (The author of the paper makes it clear that, 
"sudden infant death syndrome has not been associated with vaccination."
[91]
 Since, 
as has been amply documented, only one-tenth of vaccine-induced reactions are 
reported to the VAERS (by some estimates, this is figure is even greater)
[92]
,
[93]
, this 
number vastly underestimates the real incidence of vaccine-associated 
complications. Furthermore, no link has been established when the adverse event 
occurs long after the time of vaccination
[94]
.  In fact, a 1998 study in the Lancet and 
a recent review claim that no link exists between the MMR vaccine and subsequent 
long-term health events such as autism or bowel obstruction.
[95] [96] [97]
Another area of concern is that many doctors refuse to vaccinate themselves 
and their families,
  [98] [99] [100]
even though physicians belong to a high-risk 
category and are urged to accept vaccinations because of their continued exposure 
to infectious disease. A 1981 article in the Journal of the American Medical 
Association reports that the lowest vaccination rate among medical personnel for 
the German measles vaccine occurred among obstetrician/gynecologists and the 
next lowest rate occurred among pediatricians.  
[101]
 The authors conclude, "The 
fear of unforeseen vaccination reactions was the main reason for the low uptake 
rate of physicians to be vaccinated." In the British Medical Journal, a 1990 article 
tells us that of 598 doctors questioned about hepatitis B vaccine, 86 percent believe 
that all general practitioners should be vaccinated against this disease. Yet 309 of 
those practitioners had not been vaccinated themselves. 
[102] [103]
  A 2004 article in 
the Journal of Occupational Medicine summarizes these findings, and others, 
including the fact that some doctors are unconcerned with regards to vaccination 
protection, while in that over 80% received Hep B inoculation, only 49% 
confirmed immune response to the virus, and only half did any preventive 
measures after needle stick injuries.
[104]Vaccinations Are Based on Unsound Principles. According to Jamie 
Murphy, "Vaccines are portrayed as being indispensable and somehow better at 
disease protection than what our innate biological defenses and nutritional 
resources have accomplished for thousands of years.... Before the introduction of 
the measles and mumps vaccines, children got measles and they got mumps, and in 
the great majority of cases those diseases were benign."
[105]
Walene James, author of Immunization: The Reality Behind the Myth,
[106]
believes that the full inflammatory response is necessary to create real 
immunity.
[107]
 James summarizes the work of Dr. Richard Moskowitz, past 
president of the National Institute of Homeopathy, as stating, "'Vaccines trick the 
body so that it will no longer initiate a generalized inflammatory response. They 
thereby accomplish what the entire immune system seems to have evolved to 
prevent. They place the virus directly into the blood and give it access to the major 
immune organs and tissues without any obvious way of getting rid of it. These 
attenuated viruses and virus elements persist in the blood for a long time, perhaps 
permanently. This, in turn, implies a systematic weakening of the ability to mount 
an effective response, not only to childhood diseases but to other acute infections 
as well.'"
Murphy observes that vaccines, unlike childhood diseases, do not produce 
permanent immunity. "The medical profession does not know how long vaccine 
immunity lasts because it is artificial immunity. If you get measles naturally, in 99 
percent of the cases, you have lifelong immunity. If you have German measles you 
will have lifelong immunity. The chances of getting measles twice, German 
measles twice, or even whooping cough twice [are remote].... However, if you get 
a measles vaccine or a DPT vaccine, [it does not give you 100% assurance]  that 
the vaccine will prevent you from getting the disease." 
[108]
     
In "Vaccination: Dispelling the Myths," Alan Phillips writes, "The clinical 
evidence for vaccination is their ability to stimulate antibody production in the 
recipient, a fact which is not disputed. What is not clear, however, is whether or 
not such antibody production constitutes immunity. For example, a-gamma globulinemic children are incapable of producing antibodies, yet they recover from 
infectious diseases almost as quickly as other children....Natural immunization is a 
complex phenomenon involving many organs and systems; it cannot be fully 
replicated by the artificial stimulation of antibody production....[Our] 
immunological reserves may thus actually be reduced, causing a generally lowered 
resistance."
[109] [110]
     
Phillips adds: "Another component of immunization theory is 'herd 
immunity,' ...when enough people in a community are immunized, all are 
protected.... there are many documented instances showing just the opposite-fully 
vaccinated populations do contract diseases; with measles, this actually seems to 
be the direct result of high vaccination rates...."
[111], [112] [113]
Writing in Nexus, Phillips makes the point that immunization practice 
assumes that all children, regardless of age and size, are virtually the same. "An 8-
pound 2-month-old receives the same dosage as a 40-pound five-year-old," Phillips 
points out. "Infants with immature, undeveloped immune systems may receive five 
or more times the dosage (relative to body weight) as older children." What's more, 
random testing has revealed that the number of "units" within doses has been found 
to range up to three times what the label indicates, with quality control tolerating a 
rather large margin of error.
Questionable Science. Many scientific studies tell us that vaccines are safe 
and effective when this is not necessarily the case. 
110 112 113
Doctors and vaccine 
proponents often quote studies done solely on antibody production in the blood, 
not taking into account clinical experiences.  We must note, however, that clinical 
experience is important, and particularly with regards to the treatment of viral 
infections that have not or cannot be treated at the time with vaccine.  For 
example, we know that transmission at the time of birth of the chickenpox virus is 
dangerous to the livelihood of the infant, and that low birth weight contributes to 
susceptibility to death from the virus
[114]
, thus indicating a possible need for 
doctors to be clinically aware of the mother's risk factors for low birth weight 
infants
[115] [116]
.  For example doctors recommend the following for the outcome of 
a healthy birth weight including no alcohol consumption, drug use, and adequate 
nutrition
[117]
 as well as regular prenatal checkups
[118]
 .  In addition to being aware of the causes of low birth weight infants, the use of the antibody titer VZIG in a 
timely manner can sometimes prevent death
[119]
.  As opposed to the chickenpox 
vaccine (which contains live, attenuated chickenpox virus), VZIG contains immune 
fractions from the blood of people that can help those who are dangerously 
immune compromised for a short period of time
[120]
.  Other non-vaccine 
alternatives are being made available for this widespread virus; the use of 
acyclovir, which has been determined to be useful in lessening the severity of 
chickenpox infection in children, might be preferable to the VZIG treatment (we 
note that VZIG does contain the preservative thimerosol
[121]
), but the use of 
acyclovir during pregnancy has not yet been widely tested
[122]
 in the clinical 
setting, and shows that much more research is needed in non vaccine alternatives.
Dr. Dean Black, author of Immunizations: Compulsion or Choice, brings up 
an issue that needs more attention-what if we stopped compulsory vaccination? 
"By looking at what happens in countries where vaccinations are no longer 
required," he says, "we can get an idea of what would truly happen if we were to 
cease demanding compulsory immunization in America. In 1975, Germany 
stopped requiring pertussis [whooping cough] vaccinations, and the number of 
children vaccinated promptly began to drop. Today, it has dropped to well below 
10 percent. What has happened in Germany from pertussis over that period of 
time? The mortality rate has continued to decrease."
[123]
The Natural Evolution of Disease. Immunization supposedly puts an end 
to disease. We attribute the decline in polio to the polio vaccine, the 
"disappearance" of smallpox to the smallpox vaccine, and so forth.
[124], [125], [126], 
[127], [128], [129]
But are vaccinations the magic bullets we believe them to be? Dr. Harris 
Coulter, an expert on the pertussis vaccine, co-author of A Shot in the Dark,
[130]
and 
author of Vaccination, Social Violence, and Criminality,
[131]
concludes 
otherwise.
[132]
 Regarding infectious diseases of the past, he states, "The incidence 
of all of these infectious diseases was dropping very rapidly, starting in the 1930s. 
After World War II, the incidence continued to drop as living conditions improved. 
Clean water, central heating...these are the factors that really affected people's 
tendencies to come down with infectious diseases much more than vaccines. The vaccines might have added a little bit to that downward curve, but the curve was 
going down all the time anyway."
Dr. Coulter's view is supported by the Australian Nurses Journal: "A careful 
study of the decline in disease will show that up to 90 percent of the so-called 
'killer diseases' had all but disappeared when we introduced immunization on a 
large scale during the late thirties and early forties."
[133]
 A similar statement is 
made by the Medical Journal of Australia: "The decline of tetanus as a disease 
began before the introduction of tetanus toxoid to the general population. The 
reasons for this decline are the same for the decline in all other infectious diseases: 
improved hygiene, improved sanitation, better nutrition, healthier living 
conditions, etc." 
Alan Phillips elaborates on this theme: "We just assume that vaccinations 
are responsible for disease decline, which is not the case. For if you check the 
statistics, you will find that the vast majority of disease decline proceeded 
vaccines. In the case of measles, for example, there was a 97 percent decline 
preceding vaccination; in the case of pertussis, 79 percent. When you look at the 
graph of the decline in death rate over the course of the century, you see that the 
rate of decline, post-immunization, was virtually the same as the decline preimmunization, suggesting that it's difficult to tell whether or not the vaccine had 
any effect on an already well-established decline in disease deaths."
[134], [135]
Phillips attacks the notion that vaccines are responsible for the dramatic 
reduction in infectious disease during this and past centuries. "According to the 
British Association for the Advancement of Science, childhood diseases decreased 
90 percent between 1850 and 1940, paralleling improved sanitation and hygienic 
practices, well before mandatory vaccination programs. Infectious disease deaths 
in the U.S. and England declined steadily by an average of about 80 percent during 
this century (measles mortality declined over 97 percent) prior to vaccinations. In 
Great Britain, the polio epidemics peaked in 1950, and had declined 82 percent by 
the time the vaccine was introduced there in 1956. Thus, at best, vaccinations can 
be credited with only a small percentage of the overall decline in disease-related 
deaths this century....
[136]Toxic Vaccine Ingredients and Manufacturing Processes. Walene James 
urges parents to think about the effects the ingredients of vaccines could have on 
their children's health: "There are three categories of ingredients. The first are 
cultured bacteria and viruses....The second ingredient in vaccinations is the 
medium in which they are cultivated. This can include...dog kidney tissue, monkey 
kidney tissue, chicken or duck egg protein, chick embryo, calf serum, pig or horse 
blood, and cowpox pus. These foreign proteins are injected directly....They are 
very toxic since they do not get filtered through the digestive process or pass 
through the liver."
"These proteins are foreign to the body, and are in a state of decomposition. 
They are composed of animal cells, and therefore contain animal genetic material. 
It is possible for the genes in these cells to be picked up by the live, attenuated 
viruses used in vaccines. These viruses then implant a foreign alien genetic 
material from animal tissue cultures into the human genetic system...."
The last category of vaccine ingredients, James says, includes stabilizers, 
neutralizers, carrying agents, and preservatives. "Many people feed their children 
healthy foods. They would never think of giving their children formaldehyde...or 
aluminum phosphate to eat....These are preservatives and carrying agents that are 
injected...without buffering by the digestive process, or censoring by the liver."
[137]
As examples of the ingredients used in vaccines, we list the contents of five 
common childhood vaccines below. These ingredients are current according to the 
latest information available to us, but they are subject to change at any time:
     
Hepatitis B vaccine: This genetically engineered, noninfectious viral 
vaccine is derived from hepatitis B surface antigen produced in yeast cells. The 
Recombivax HB vaccine (Merck & Co.) uses a fermentation medium consisting of 
a yeast extract, soy peptone, dextrose, amino acids and mineral salts. The protein is 
purified, then treated with formaldehyde and coprecipitated with alum (potassium aluminum sulfate) to form bulk vaccine adjuvanted with amorphous aluminum 
hydroxyphosphate sulfate. There is no detectable yeast DNA in the vaccine, but it 
may contain not more than 1% yeast protein.
[138]
 For the Engerix-B vaccine 
(SmithKline Beecham), the antigen is absorbed on aluminum hydroxide, and the 
product contains no more than 5% yeast protein. The product also contains sodium 
chloride and phosphate buffers. The pediatric/adolescent and adult formulations of 
Engerix-B do not have preservatives but may contain a trace amount of thimerosal 
(a mercury derivative) from the manufacturing process.
[139]
 Recombivax HB is 
supplied in pediatric/adolescent and adult formulations with and without a 
preservative.
[140]
     
DPT vaccine: This vaccine includes diphtheria and tetanus toxoids and 
acellular pertussis vaccine absorbed. The components of the acellular pertussis 
vaccine are isolated from phase 1 Bordetella pertussis culture grown in a modified 
Stainer-Scholte medium. They are treated with formaldehyde. For the Tripedia 
vaccine (Aventis Pasteur), the Corynebacterium diphtheriae cultures are grown in 
a modified Mueller and Miller medium, while the Clostridium tetani cultures are 
grown in a peptone-based medium containing a bovine (meat) extract. Both are 
treated with formaldehyde, and the detoxified materials are purified by serial 
ammonium sulfate fractionation and diafiltration. The toxoids are absorbed using 
aluminum potassium sulfate (alum). The product contains sodium chloride, gelatin, 
and polysorbate 80. The one-dose vial does not have a preservative but contains a 
trace amount of thimerosal from the manufacturing process; the multidose vial 
contains thimerosal as a preservative.
[141]
 For the Infanrix vaccine (SmithKline 
Beecham), the diphtheria toxin is produced in a Linggoud and Fenton medium 
containing a bovine extract, and the tetanus toxin is produced in a modified 
Latham medium. Both are treated with formaldehyde, and each is absorbed onto 
aluminum hydroxide. The product contains 2-phenoxyethanol as a preservative, 
sodium chloride, and polysorbate 80.
[142]
     
Inactivated polio vaccine: The IPOL product (Aventis Pasteur) is a highly 
purified, inactivated vaccine that contains three types of poliovirus. The viruses are 
grown in cultures of VERO cells, a continuous line of monkey kidney cells. The 
cells are grown in Eagle MEM modified medium, supplemented with newborn calf 
serum that is tested for adventitious agents before use and originates from 
countries free of bovine spongiform encephalopathy. For viral growth, the culture medium is M-199, without calf serum. (The residual calf serum protein is less than 
1 ppm in the final vaccine.) Neomycin, streptomycin and polymyxin B are used in 
the production process. The vaccine also contains 2-phenoxyethanol and 
formaldehyde (0.02% maximum) as preservatives.
[143]
MMR vaccine: The M-M-R II live virus vaccine (Merck & Co.) contains 
(1) Attenuvax, a more attenuated line of measles virus propagated in chick embryo 
cell culture; (2) Mumpsvax, a strain of mumps virus propagated in chick embryo 
cell culture; and (3) Meruvax II, the Wistar RA 27/3 strain of live attenuated 
rubella virus propagated in WI-38 human diploid lung fibroblasts. The product 
contains sorbitol, sodium phosphate, sucrose, sodium chloride, hydrolyzed gelatin, 
human albumin, fetal bovine serum, and neomycin. It does not contain a 
preservative.
[144]
Chickenpox vaccine: The Varivax vaccine (Merck & Co.) is prepared from 
the Oka/Merck strain of live, attenuated varicella virus. The virus originated from a 
child with natural varicella. It was introduced into human embryonic lung cell 
cultures, adapted to and propagated in embryonic guinea pig cell cultures and 
propagated in human diploid cell cultures (WI-38). The vaccine contains sucrose, 
hydrolyzed gelatin, sodium chloride, monosodium L-glutamate, sodium phosphate 
dibasic, potassium phosphate monobasic, potassium chloride, residual components 
of MRC-5 (human diploid) cells including DNA and protein, and trace amounts of 
sodium phosphate monobasic, EDTA, neomycin, and fetal bovine serum. There is 
no preservative.
[145]
Noting that vaccines include a host of undisputed toxins, such as aluminum 
phosphate and formaldehyde, Alan Phillips reminds us that many of the ill effects 
of vaccines did not exist at anywhere near today's levels 30 years ago. He cites 
autism, ADD, hyperactivity, dyslexia, and a host of allergies as examples.
[146]
In his book What Every Parent Should Know About Childhood 
Immunization, Jamie Murphy seconds the views of Phillips: "What could 
formaldehyde, aluminum, phenol...or any number of other deadly chemical substances used in vaccines possibly have to do with preventing disease in 
children? The fact that they are needed at all in the vaccine formula argues that the 
product is toxic, unstable and unreliable with or without their presence."
[147]
The Use of Thimerosal. In July 1999, the American Academy of Pediatrics 
(AAP) issued a statement urging the removal of the mercury-containing 
preservative thimerosal from vaccines.
[148]
 The Centers for Disease Control and 
Prevention (CDC) reported that as of April 2001, all seven of the vaccines 
recommended for use in all children contained either no thimerosal or trace 
amounts only. These vaccines include hepatitis B, Haemophilus influenzae B, and 
DTaP (which formerly contained thimerosal as a preservative) and MMR, polio, 
varicella and pneumococcal (which have never contained thimerosal).
[149]
The FDA explains that the vaccines are now being produced as either 
thimerosal-free or thimerosal-reduced products. The term thimerosal-reduced, it 
says, usually indicates that trace amounts of mercury-less than 0.5 micrograms per 
0.5 mL vaccine dose-may remain from the use of thimerosal in the manufacturing 
process, but that thimerosal is not added as a preservative. The term preservativefree means the vaccine does not have a preservative but, again, that trace amounts 
may remain from the manufacturing process.
[150]
The reason for the AAP's strong recommendation in 1999 was a growing concern 
about the risk of exposing the developing brains of infants to mercury. As more 
vaccines were being mandated for children, the cumulative level of mercury 
exceeded that deemed safe by guidelines. With the new pediatric vaccines, the 
FDA says, "the most likely maximum amount of ethyl mercury that an infant may 
be exposed to from the routine vaccination schedule has been reduced from 
approximately 187.5 mcg to <3 mcg."
[151]
While this change is certainly welcomed, we should ask why such a dangerous, 
known neurotoxin was allowed to be used in vaccines in the first place. Mercury 
exposure has been associated with nerve cell degeneration,
[152]
 adverse behavioral 
effects,
[153]
 and impaired brain development.
[154]
 It has also been linked to degenerative chronic conditions such as Alzheimer's disease. The developing fetal 
nervous system is the most sensitive to its toxic effects, and prenatal exposure to 
high doses of mercury has been shown to cause mental retardation and cerebral 
palsy.
[155]
Yet the CDC recommends the influenza vaccine, which for the most part 
still contained mercury until late 2002, to all pregnant women, despite the 2001 
urging from the Institute of Medicine that "full consideration be given to removing 
thimerosal from any biological product to which infants, children, and pregnant 
women are exposed." The CDC's homepage, today, September 6, 2006, quotes, 
"Today, with the exception of some Influenza (flu) vaccines, none of the 
vaccines used in the U.S. to protect preschool children against 12 infectious 
diseases contain thimerosal as a preservative."
This means that some of the country's most vulnerable, are still receiving 
mercury in its shots, as the flu vaccine is recommended for those most at risk, 
including the elderly, those with weakened immune systems, and very young 
children.
In 2001 the FDA was in discussions with manufacturers of influenza virus 
vaccines regarding the development of thimerosal-free or -reduced products.
[156]
According to the CDC, one manufacturer of influenza vaccine, Evans Vaccines, 
had reduced-thimerosal influenza vaccines available by the 2002-2003 flu season. 
This Fluvirin product had less than 1 mcg of thimerosal per dose; other influenza 
vaccines at the time had 25 mcg.
[157]
 For the pediatric market, another 
manufacturer, Aventis Pasteur, announced in September 2002 that the FDA had 
approved a license to market a preservative-free influenza vaccine for infants aged 
six to 35 months. A supply of the preservative-free Fluzone was available for the 
2002-2003 flu season.
[158]Despite the change over, this still begs the question as to how many children are 
still suffering the effects of mercury-toxic injections from as late as the 2000 and 
2001 flu seasons.
It should also be noted that while the mercury content of childhood vaccines has 
been eliminated or greatly reduced, vaccines may still contain formaldehyde (a 
highly carcinogenic material used to embalm corpses) and/or aluminum.
New vaccines continue to be approved:  in 2003 the "first live attenuated 
influenza vaccine licenced for 5-49 year old persons"
[159]
 was approved, and in 
2004 "inactivated influenza vaccine was recommended for all children 6-23 
months of age"
[160]
However, the CDC site does not state specifically which flu 
vaccinations contain the thimerosol: "certain Influenza (flu) vaccines and tetanusdiphtheria vaccines (Td) given to children age 7 and older contain thimerosal as a 
preservative."
Unproven Vaccines, Unmonitored Medicine The widespread use of 
experimental vaccines during Desert Storm has often been cited as a possible cause 
of Gulf War syndrome. Dr. Garth Nicolson elaborates: "I'm not a big fan of 
experimental vaccines. There have been too many mistakes. Usually you find these 
things out years later. Often agents that we think innocuous turn out to be 
harmful." He explains that during the Gulf War, the established procedures of 
vaccination were ignored. Normally, only one inoculation should be given at a 
time, but the military insisted on giving multiple shots at once, which, according to 
Nicolson, is the worst thing you can do because it suppresses the immune system. 
[5]
The troops immunized for the Gulf have been called guinea pigs, and for 
good reason. They received experimental vaccines, e.g., those for anthrax and 
botulinum that were not approved for use by the FDA and have since proven to 
cause potentially dangerous side effects. In 1991,  "Anthrax vaccine was 
administered to about 150,000 troops in the [Gulf War] theater, about 1/5 of those 
deployed."
[161]
 Soldiers who were given these experimental vaccines, without 
informed consent, have reported suffering from a variety of neurological problems 
and aberrant bleeding from all parts of their bodies. Because of these vaccines' 
experimental nature, many questions have arisen as to why our government 
dispensed them. Not the least of these questions is, what about the Nuremberg Code? Developed by the Allies after World War II in response to inhumane Nazi 
experimentation, the Nuremberg code says that voluntary and informed consent is 
absolutely essential from all human subjects who participate in research, whether 
during peace or war. [11]
Vaccine Failures. According to Phillips, "The medical literature has a surprising 
number of studies documenting vaccine failure. Measles, mumps, smallpox, and 
polio outbreaks have all occurred in vaccinated populations. In 1989, the CDC 
reported: Among school-aged children, [measles] outbreaks have occurred in 
schools with vaccination levels of greater than 98 percent. They have occurred in 
all parts of the country, including areas that had not reported measles for years. 
The CDC even reported a measles outbreak in a documented 100 percentvaccinated population. A study examining this phenomenon concluded, 'The 
apparent paradox is that as measles immunization rates rise to high levels in a 
population, measles becomes a disease of immunized persons.'...These studies 
suggest that the goal of complete immunization is actually counterproductive, a 
notion underscored by instances in which epidemics followed complete 
immunization of entire countries....In the U.S. in 1986, 90 percent of 1,300 
pertussis cases in Kansas were 'adequately vaccinated.' Seventy-two percent of 
pertussis cases in the 1993 Chicago outbreak were fully up to date with their 
vaccinations."
[162], [163], [164], [165], [166], [167], [168], [169], [170]
Effects of Specific Vaccines
With this section, we begin an examination of the effects of specific 
vaccines. Seven vaccines will be covered in this and the next two installments of 
this series: diphtheria, pertussis and tetanus, polio, chickenpox, hepatitis B, 
measles, mumps and rubella, smallpox, and the now-withdrawn rotavirus vaccine.
DIPHTHERIA, PERTUSSIS, AND TETANUS VACCINES
Diphtheria Vaccine
In the 15 years following the introduction of the diphtheria vaccine in 1894, 
the number of deaths in England and Wales rose 20 percent. Between 1895 and 
1907, there were 63,249 cases of diphtheria in individuals treated with anti-toxin; 8,917 people died, a fatality rate of 14 percent. In the same time period, there were 
11,716 cases not treated with anti-toxin; only 703 died, a fatality rate of 6 percent.
From a book by Greg Beattie, entitled, "Vaccination A Parent's Dilemma," 
we examine official charts taken from the Commonwealth of Australia, on the 
decline in death rates from Whooping Cough, Diptheria, measles, and Scarlet 
Fever.  We see that in each case, the bulk of the death rates from each illness 
declined in large measure even before the vaccine for the illness had been given.  
Lest we think, however, that these may be figures unique to Australia, the author 
states that, "Graphical evidence on the decline in death rates from infectious 
disease for USA, England, New Zealand and many other countries shows the exact 
same scenario[s]"  Whooping cough death rates, for example, when the 
vaccinations were given, between 1940 and 1960, had already declined to almost a 
tenth of their original rate at their height in 1880.  During the decade between 1940 
and 1950, when the Diptheria vaccine was originally given, death rates had 
declined to almost a quarter of their rate in 1880, and the measles deaths, at their 
height in the 1900's, had already declined to its modern low rates by the mid 
1960's, when the first vaccine was given.  
The CDC's paper on reduction of illnesses in the 20
th
 century mentions that 
one of illnesses that was reduced to zero by the year 2004, was diptheria, from an 
average of 21, 053 deaths per year in the 20
th
 century.
We know from Greg Beattie's work that the earliest vaccinations for childhood 
illnesses were given in the late 1930's for diptheria.  When we  examine the figures 
from the Union soldiers'study, mentioned earlier; we note that only the last of the 
children for the later cohort (1918-1927) would have been children when the 
Diptheria vaccinations were given.   Although heart damage can occur in untreated 
Diptheria cases, most Diptheria onset occurs in adolescents and adults.  Most of the 
later cohort would already have been adolescents at the time of the Diptheria 
vaccine, so it is unlikely that the onset of the Diptheria vaccination alone had an 
effect on the outcome of delayed onset of heart disease already noted in this group 
of people. 
47 48 49 50Similarly, it may be true that childhood illnesses could have a role in the formation 
of joint inflammation later in life, but again, only the last children of the later 
cohort in the union soldiers' study would have received the Diptheria vaccine in 
later childhood, so this would have a negligible effect on the outcome of all joint 
pain in this cohort group.  
Acellular Pertussis Vaccine
Until 1996 the whole-cell vaccine was the only whooping cough vaccine 
available in the U.S. for children in their first year of life. This vaccine included all 
the components of the bacterium Bordetella pertussis, including the toxic ones, and 
was associated with high rates of adverse reactions. In Japan, a lack of trust among 
the public of the whole-cell vaccine led to the development of a new, purified 
acellular vaccine that has been used exclusively in the country since 1981.
[171]
Even though a safer vaccine was widely used in Europe and Japan, it wasn't 
until 15 years later that the purified acellular pertussis vaccine was approved by the 
U.S. FDA for use in combination with the diphtheria and tetanus toxoids for all 
doses in the vaccination series.
[172]
 A 1996 study showed that the rate of adverse 
reactions reported to VAERS in 1991 to 1993 dropped from 9.8 per 100,000 
vaccine doses to 2.9 per 100,000 after substitution of the acellular pertussis vaccine 
for the whole-cell vaccine for the fourth and fifth dose of DPT vaccination.
[173]
Vaccine Failure. Ninety-one percent of pertussis cases in Nova Scotia, 
Canada, had received at least three doses of vaccine. Researchers concluded that 
"pertussis remains a significant health problem in Nova Scotia despite nearly 
universal vaccination."
[174]
 In this case, the pertussis vaccination proved 
ineffective.
Pertussis vaccination also has been shown to increase the susceptibility of 
certain individuals to the infection, as a 1997 report by the CDC clearly describes. In the Netherlands, 96 percent of children have received at least three shots of 
pertussis vaccine by the age of 12 months. Yet pertussis has been endemic in the 
country for the past two decades.
[175]
Increasing Cases of Pertussis in Infants and Adults. After the United 
States mandated pertussis vaccination in 1978, the incidence of the disease in the 
following eight years trebled. While cases of pertussis were increasingly seen 
among every age group, the highest incidence was registered in infants less than 1 
year old, and the highest relative increase was seen in adolescents and adults. It is 
important to note that infants suffered from the most complications, with rates of 
hospitalization, pneumonia, convulsions, and encephalopathy being the highest in 
children 0 to 6 months old.
[176]
According to one article, the incidence of pertussis increased each year in 
England and Wales after an accelerated immunization schedule was introduced.
[177]
Since the immunity provided by the vaccine, unlike that derived from natural 
infection, is only temporary, more adults are now contracting the disease and are 
transmitting it to infants, where the infection manifests with particular severity and 
can often lead to death.
Epidemics of pertussis striking infants have also been reported in Australia, 
despite extensive vaccination coverage.
[178]
DPT Safety. The U.S. Department of Health and Human Services estimates 
that every year approximately half a million DPT shots are followed by reactions 
severe enough to contraindicate the administration of more pertussis vaccine. One 
in seven children should be turned away for further pertussis vaccine. In practice, 
though, this does not happen. 
[179], [180]
 And, as pointed out by Alan Phillips, "The 
FDA's VAERS (Vaccine Adverse Effects Reporting System) receives about 11,000 
reports of serious adverse reactions to vaccination annually, some 1 percent (112+) 
of which are deaths from vaccine reactions. The majority of these deaths are 
attributed to the pertussis (whooping cough) vaccine, the 'P' in DPT. This figure alone is alarming, yet it is only the tip of the iceberg. The FDA estimates that only 
about 10 percent of adverse reactions are reported...."
DPT Vaccination and Neurological Damage. The scientific literature 
contains documentation of the damaging effects of DPT vaccination on the nervous 
system. Neurological complications include convulsions, hypotonichyporesponsive episodes (a collapse-shock-like status), paralysis, and 
encephalopathy.
FURTHER READINGS: Articles in the literature associate DPT 
vaccinations with neurological problems
[181], [182]
and convulsions.
[183], [184], [185], [186]
DPT Vaccination and Asthma. In a 1994 study published in the Journal of 
the American Medical Association, Dr. Michel Odent found that children 
immunized against whooping cough were five times more likely to suffer from 
asthma than those who did not receive the vaccine.
[187]
Dr. Odent's is not a solitary voice. Another study, performed by Farooqi et 
al. on almost 2,000 children born between 1974 and 1984, showed that vaccination 
against whooping cough is associated with a 76 percent increased risk of 
developing asthma and other allergic diseases later in life.
[188]
     
DPT Vaccination and SIDS. Sudden infant death syndrome (SIDS) is the 
unexpected death of a child occurring without any apparent explanation, and for 
which autopsy cannot reveal a determining cause. Every year, 5,000 to 6,000 
children die from SIDS. The incidence peaks in infants aged 2-4 months, which 
correlates with the introduction of a majority of vaccine injections. It is worth 
noting that approximately 85 percent of SIDS cases occur during the first six 
months of life, and that the first three DPT shots were given to children at 2, 4, and 
6 months of age when these studies were conducted.A study conducted by researchers at the Mayo Clinic looked at the incidence 
of SIDS in Olmsted County, Minnesota, over several decades and found that it 
increased steadily from a rate of 0.55 per 1,000 live births in 1953 to 128 in 1992. 
That's a great increase in this 40-year study period. However, when the authors 
compared mortality from SIDS to overall infant mortality, they came up with an 
even more distressing finding. The increase of SIDS as a percentage of total infant 
deaths increased from 2.5 in 1953 to 17.9 in 1992.
[189]
 So from 1950 to 1990, a 
combination of lifestyle changes, improved sanitary conditions, and progress in 
medical technology resulted in a reduction of practically all causes of infant death 
except one-sudden infant death.
In 1982, at the 34th Annual Meeting of the American Academy of 
Pediatrics, Dr. W. Torch presented an abstract entitled "Diphtheria-PertussisTetanus (DPT) Immunization: A Potential Cause of the Sudden Infant Death 
Syndrome (SIDS)." Triggered by a report of 12 such deaths occurring within 3-1/2 
to 19 hours of DPT vaccination, Torch's investigation looked at 70 SIDS cases. He 
found that two-thirds of the victims had been vaccinated from a half day to three 
weeks prior to death.
[190]
Torch reaffirmed a link between DPT and SIDS in 1986, when he presented 
11 new cases of SIDS and one of near-miss syndrome (NMS) occurring within 24 
hours of DPT injection. All cases presented with SIDS pathology, yet none were 
diagnosed as "postvaccinal" death.
[191]
 Analysis of these and other more than 150 
cases of DPT postvaccinal deaths reported in the literature-about half of which 
were sudden or anaphylactic-led Torch to conclude that "Although many feel that 
the DPT-SIDS relationship is temporal, this author and others maintain a casual 
relationship exists in a yet-to-be-determined SIDS fraction."
[192]
 Other researchers 
also have uncovered a relationship between DTP immunization and SIDS.
[193], [194]
Tetanus Vaccination and Neurological Damage. The literature includes 
articles on neurological reactions to the tetanus vaccination
[195], [196], [197], [198], [199], 
[200]
 and other adverse reactions.
[201], [202], [203]In Part 2: The effects of vaccines for polio, chickenpox, hepatitis B, and 
measles, mumps and rubella.
Vaccination: Pain, Profit, and Politics - Part 2
By Gary Null, Ph.D., and Martin Feldman, M.D.In Part 1 of this series, we discussed the reasons why we should challenge our 
assumptions that vaccines are safe and effective. These reasons include the adverse 
effects associated with vaccines, the unsound principles on which they are based, 
questions about whether immunization really eliminates disease, the toxic 
ingredients used in vaccines, and vaccine failures. In Part 1 we also began to look at 
the effects of specific vaccines with a discussion of the diphtheria, pertussis and 
tetanus vaccine; we continue that process in Part 2 with a look at the polio, 
chickenpox, hepatitis B, and measles, mumps and rubella vaccines.
Polio Vaccine
Three types of polio vaccines have been used throughout the world: 1) the 
OPV, or oral polio vaccine (Sabin vaccine), consisting of live, attenuated poliovirus; 
2) the IPV, or inactivated polio vaccine (Salk vaccine), consisting of killed 
poliovirus and given by injection; and 3) the eIPV, an enhanced potency inactivated 
polio vaccine, consisting of killed poliovirus with high viral antigen content.
Today, the Advisory Committee on Immunization Practices (ACIP) 
recommends exclusive use of the IPV for routine childhood polio vaccination in the 
U.S. (the enhanced-potency version is the only IPV in use in the U.S.). The ACIP 
changed its polio vaccine recommendation to the all-IPV schedule, effective January 
2000, to eliminate the risk for vaccine-associated paralytic poliomyelitis (VAPP), 
the condition caused by the previously recommended oral polio vaccine.
[204]
Until 1996, all children in the U.S., except those with a compromised immune 
system and their close contacts, were immunized with the live attenuated OPV 
vaccine. However, the vaccine actually caused polio in a small percentage of people. 
According to the CDC, the overall risk for VAPP is approximately one case in 2.4 
million OPV doses distributed, while the first-dose risk is one case in 750,000 doses distributed. In fact, the only indigenous cases of polio reported in the U.S. since 
1979 have been associated with the use of OPV. Between 1980 and 1998, 144 cases 
of VAPP were reported.
[205]
Despite these occurrences, the ACIP recommended the use of OPV in the U.S. 
because it believed the benefits of the oral vaccine outweighed the risk for VAPP. In 
1996, the ACIP recommended a sequential schedule of IPV and OPV to "decrease 
the risk for VAPP but maintain the benefits of OPV." It then recommended the allIPV schedule as of January 2000, citing several reasons: the substantially reduced 
likelihood of poliovirus being imported into the U.S. due to rapid progress made in 
the global polio eradication initiative; the acceptance of the sequential schedule; and 
the lack of declines in childhood immunization coverage.
[206]
The CDC states that, "in 1955 the inactivated polio vaccination was 
licenced."
[207]
  In 1954, the largest vaccination trial to date was undertaken across the 
country.  Up to 600,000 children throughout the country were vaccinated due to 
efforts by parents, community activists, and teachers, both in the efforts of pursuing 
science and bettering public health.  Children and their parents were told that they 
were 'pioneers' in an effort to eradicate a debilitating scourge.  In homage to the 
passionate public effort, researchers stated that 95% of children received the three 
shots required by the trial.    Whereas the design of the study was vigorous, there 
were complaints as to the follow through. The setup of the study was as follows: 
Each child received three vaccinations on a rigorous schedule, and the two arms of 
the study had differing control groups which would even out the counterbalancing 
effects of income, nutrition, and class; however, it was often reported that the entire 
dose was not given per child, or that in the control group which was to have received 
a placebo injection, liquid from the experimental group remained in the syringe, 
thereby giving the placebo child a weak inoculation.  Despite the fact that the 
government review of the outcome of polio vaccination was to have been considered 
positive, critics said that there was not a huge difference between the observed and 
placebo control groups and the actual groups that received the vaccinations.
In three of the trial groups, numbers of children in the study tested were 
between 200,000 and 225,000.  In order to compare effectiveness, we will average 
the outcomes based on numbers tested at 200,000:Therefore, for in areas where a placebo shot was given, along with the 
vaccination, an average of 32.87 children came down with polio out of 200,000 who 
received the shots, whereas an average of 114.30 children out of 200,000 came down 
with the illness who did not receive the vaccination.  
In the next cohort group, an average of 34.24 children out of 200,000 came 
down with polio after receiving the vaccination whereas an average of 91.01 
children out of 200,000 came down with polio in the control group who was just 
observed rather than actually receiving the shots.  Although the numbers for the two 
arms of the study may be similar, it appears that the lower number in the 
observational control may be slightly more accurate for a couple of reasons:  First, 
there were complaints that the actual givers of the vaccines contaminated the control 
groups with the active vaccine, and second, the control group of observed children 
was much larger than the control group who received a placebo [725, 123 as 
compared to 201, 229 in the placebo group];  it is well known that a larger cohort 
group is desired for better scientific accuracy.
The one positive aspect of the placebo arm of the study as noted by author 
David Oshinsky was that the children were more likely to be of the same age, class, 
and upbringing, since those who were vaccinated tended to have parents who were 
better educated and more willing to commit their children to a scientific study for the 
'betterment of scientific inquiry'.  It is just such attitudes that we wish to examine 
closely in this paper, for these are the vulnerabilities that the mainstream medical 
community uses when coercing the public to use vaccinations.
[208]
After the auspicious start as seen by the CDC's National Immunization 
program, we will examine the timeline for the various vaccinations given in the US:
Polio was seen originally as a mystery because the sanitation measures that had 
brought typhoid and cholera into abeyance did not seem to have an effect on polio.  In fact children brought up in middle class homes were more likely to develop the 
paralyzing illness than those in poorer neighborhoods.  
For example: "[Franklin Roosevelt] had avoided the common illnesses until his 
arrival at boarding school as a teen.  From that point forward, his medical history 
resembled an encyclopedia of contagious diseases.  The list included typhoid fever, 
swollen sinuses, infected tonsils, stomach problems, endless sore throats."
[209]
  We 
know that later he was said to have contracted polio but some have attributed his 
illness to Guillain Barre syndrome as well, which we see below, has an association 
with Polio.
Originally, The Polio outbreaks were one of the first times it was suggested that 
a less-antiseptic environment may have had a protective effect upon the child.  It was 
later found that polio was a viral infection, and was passed through the mouth,
[210]
but was an infection of the digestive tract that spread through the nerves to the brain 
and spinal cord.  One of the early researchers on polio noticed that boys tended to 
get polio more often than girls, and during periods where they had stressed their 
bodies, such as playing outside on a hot day.  Franklin Roosevelt was said to have 
contracted polio after playing rigorously in the water with his children.  
Whether rich or poor, however, author David Oshinsky points not to large 
issues of public sanitation, but to issues of personal hygiene: 
"the words 'American' and 'cleanliness' rarely graced the same sentence before 
the twentieth century.  In 1900 toothbrushes were still rare in the United States, 
deodorants and shampoos almost unheard of.  Few people bathed more than once a 
week or rinsed their hair more than once a month.  Fewer still washed their hands 
before eating or after using the toilet.  Spitting was almost universal.  Travelers 
shared beds and chamber pots with complete strangers.  Most houses, lacking 
screens, attracted swarms of insects in warm weather.  Water supplies were 
unfiltered, and food was poorly refrigerated, if at all."
[211]It is clear to anyone with a modicum of common sense that these would be ideal 
conditions to spread a virus of the digestive tract.  In an article entitled Introduction 
to Contagion
[212]
, we discover that it is important to note the way a disease is 
transmitted when examining the ways in which the epidemics have happened 
throughout the ages:
For example: whether virus or bacteria, there are illnesses that are spread 
through droplets that are ingested, which are present in the air due to respiratory 
expulsion.  There are also water borne illnesses, that can be picked up by a cut in the 
skin or when a person ingests quantities of water from an infected source.  Other 
diseases can be transmitted through food, and still others through physical touching, 
such as through the hands, through the saliva, or through sexual contact.
In an epidemic of cholera, for example, the CDC states that,"the source of the 
contamination is usually the feces of an infected person. The disease can spread 
rapidly in areas with inadequate treatment of sewage and drinking water."
[213]
David Oshinsky writes of non-polio outbreaks:  
"mortality rates had dropped dramatically since the 1870's, the result of better 
sanitation, a healthier diet, and stunning breakthroughs in research...Other epidemic 
diseases like cholera and typhoid fever had been tamed by better sanitation, 
attacking the filth that spread their deadly germs.  In most places this involved the 
regulation of sewage, the purification of water, and the pasteurization of milk.  It 
included public health campaigns to educate people about quarantining the sick and 
keeping their dwellings clean."
[214]
Guillain-Barre Syndrome and Polio Vaccine. Guillain-Barre syndrome 
(GBS) is a disease that involves the nervous system and is characterized by muscle 
weakness, numbness, loss of reflexes, and paralysis. In Finland in 1985 there was an increase in the incidence of Guillain-Barre 
syndrome that followed by a few weeks the implementation of a nationwide oral 
poliovirus vaccine campaign.
[215], [216]
 And in Brazil, analysis of 38 cases of paralysis 
diagnosed as GBS led in all cases to the isolation of the vaccine strains of the 
poliovirus. All patients had been vaccinated with the oral polio vaccine months or 
years before the onset of symptoms.
[217]
Furthermore, vaccine viruses also have been isolated from patients with 
paralysis diagnosed as transverse myelitis (TM), and in patients with facial paralysis 
(FP).
[218]
 Most individuals with TM and FP had received the oral polio vaccine 
months or years prior to the onset of disease, indicating that the virus may remain 
latent and revert to virulence later in time. It is noteworthy too that in Brazil, cases 
of wild-type poliomyelitis have not been reported since 1989, while vaccineassociated paralysis is still occurring.
[219]
The Cancer Connection to the Polio Vaccine. In 1960 it was discovered that 
both the Salk and Sabin vaccines, which had been administered to millions of 
people, were contaminated with SV40 (simian virus 40), derived from the monkey 
kidney cells used to grow the vaccine viruses. The SV40 survived inactivation with 
formaldehyde, the method used to kill the poliovirus, and was therefore injected with 
the vaccine into 98 million people in the U.S.
[220]
 and hundreds of millions 
worldwide. These individuals today have SV40 sequences integrated into their 
genetic code. 
Animal studies have demonstrated the ability of SV40 to integrate its DNA into 
that of the host cell and to induce malignancy. Unfortunately, a growing number of 
studies are showing that the virus retains these same properties in humans as well as 
in animals. Integration and replication of SV40 has been documented in 13 percent 
of non-Hodgkin's lymphomas,
[221]
 16 percent of Hodgkin's lymphomas,
[222]
 11 
percent to 90 percent of different types of brain tumors,
[223],[224],[225],[226]
 83 percent of 
mesotheliomas (malignant tumors of the lining of the lungs),
[227]
 28 percent of 
bronchopulmonary carcinomas,
[228]
 50 percent of osteosarcomas,
[229]
 and more than 
33 percent of other types of bone tumors.
[230],  [231]Chickenpox Vaccine
In 1995 the American Academy of Pediatrics (AAP) and the ACIP 
recommended universal chickenpox (varicella) vaccination of children aged 12 to 18 
months. They also recommended that the vaccine be given to children aged 18 
months to 12 years who have not been vaccinated or who lack a reliable history of 
the disease.
The fact is that in the vast majority of cases, chickenpox is a benign, selflimiting disease in children. Natural immunity, derived from contracting the disease, 
is permanent. Vaccine-induced immunity, on the other hand, is only temporary, 
lasting an estimated six to 10 years. The temporary nature of vaccine-induced 
immunity can create a more dangerous situation by postponing the child's 
vulnerability until adulthood, when death from the disease is 30 times more likely.
The National Vaccine Information Center (NVIC), Vienna, Va., advises parents 
to seriously consider not using the chickenpox vaccine on healthy children. Barbara 
Loe Fisher, cofounder and president of the NVIC, elaborates: "Our organization is 
questioning the recommendation...that all healthy children be vaccinated with the 
chickenpox vaccine....
"...In children, chickenpox is, by and large, a very mild disease. The 
case/fatality ratio in healthy children is 1 death per 100,000 children. In adults it 
rises to 31 deaths per 100,000. So it basically is an experiment. That is really what 
happens with most of these vaccines that they bring out. They really don't know 
what the long-term effect is going to be. 
"The other thing about the chickenpox vaccine is that the vaccine virus could lie 
dormant in vaccinated individuals, and then reactivate later in life in the form of 
herpes zoster, which is also known as shingles, or perhaps [in the form of] other 
immune system disorders...." Fisher is not the only one to question the appropriateness of the official 
recommendations concerning this vaccination. According to the results of one 
survey, 58 percent of pediatricians interviewed did not recommend varicella 
vaccination of all infants.
[232]
Discounting the numerous concerns of doctors, researchers, and parents, in 
February 1999 the CDC expanded its guidelines for varicella vaccination and 
required that all children entering child care centers and elementary and middle 
schools receive varicella vaccination unless they have evidence of immunity.
[233]
In the meantime, 6,580 adverse events-including 14 deaths-were reported to the 
Vaccine Adverse Events Reporting System in association with varicella vaccination 
between March 17, 1995 and July 25, 1998.
[234]
 The actual number could be at least 
10 times higher, if we take into consideration the proven fact that only 10 percent of 
adverse events are commonly reported.
Another concern regards pregnant women. Normally, 90 percent of adult 
women are immune to varicella and transfer this immunity to their babies during 
pregnancy. But the immunity induced by vaccination, which lasts only five to 10 
years, may be gone by the time a woman enters her reproductive stage, leaving 
pregnant women at risk of contracting the infection and transmitting it to the fetus. 
Fetal varicella syndrome is characterized by multiple congenital malformations and 
is often fatal for the fetus.
[235]
 Thus, we need lifelong immunity from natural 
infection.
In addition, children born from women whose vaccine-induced immunity has 
faded are unprotected during their first year of life, when their immune system is 
still developing, and may suffer fatal complications should they be exposed to the 
infection.Is the Chickenpox Vaccine Effective? If the effectiveness of the vaccine is 
measured by its ability to prevent the disease from occurring, the answer is simply 
no. As we read in an article published in Pediatrics, "In 1998, three years after 
vaccine licensure, child care centers in Los Angeles County continued to report 
varicella outbreaks." These outbreaks occurred in child care centers with high 
vaccine coverage as well as in those with low coverage, meaning that the infection 
spread regardless of child vaccination status.
[236]
An interesting article clearly shows how questionable the data are claiming 
reductions of diseases following immunization campaigns. This is what often 
happens: Reporting of a specific disease is encouraged until the start of a vaccination 
program. Thus, the disease appears to be present at certain rates. Then, after the 
vaccine enters the market, reporting is no longer required and therefore not done, 
and the rates of the disease seem to drop. But in reality the drop results from changes 
in reporting requirements and practices, not from an actual decline in the number of 
cases.
Vaccination against chickenpox will not prevent a child from contracting the 
disease. Rates of infection in vaccinated individuals-so-called "breakthrough 
varicella"-range from 18 percent to 34 percent in the 10 years following 
immunization.
[237], [238], [239]
 Furthermore, even if vaccination reduces the number of 
skin lesions, the duration of the infection, and the occurrence of fever in individuals 
who develop breakthrough disease, it does not reduce the rate of constitutional 
complaints and that of complications.
[240]
One study found that 18.6 percent of children who responded to varicella 
vaccination developed breakthrough disease after exposure to the infection in the 
five to 10 years following immunization.
[241]
 Another study showed that 20-30 
percent of vaccinees developed varicella in the 10 years following immunization.
[242]
In a third study, 34 percent of individuals vaccinated against chickenpox developed 
breakthrough disease in the seven to 10 years following immunization.
[243]FURTHER READINGS: Articles discuss the potential downside to the mass 
use of the chickenpox vaccine and reactions associated with it.
[244], [245],  [246]
Hepatitis B Vaccine
The hepatitis B vaccine, commercially available in the United States since 
1982, was supposed to be given to every American child within 12 hours of birth. In 
spite of this measure, "the incidence of acute hepatitis B in this country has risen 
from 55 per 100,000 in 1981 to 63 per 100,000 in 1987," according to the New 
England Journal of Medicine.
[247]
          Additionally, strong side effects have been 
reported following the use of this vaccine. In 1990, the Journal of Pediatric Child 
Health had this to say on the subject: "There have...been reported six serious 
illnesses in a series of 200,000 hepatitis vaccinations, including aseptic meningitis, 
grand mal seizure, and possible transverse myelitis, as well as 56 minor illnesses 
considered likely due to the vaccine. These minor illnesses include neurological 
tremors, Bell's palsy, hives, herpes zoster, psoriasis, musculoskeletal generalized 
myalgia, joint inflammation...influenza-like syndrome, injection site reaction, 
diarrhea, vomiting, and headache." 
The authors conclude with these recommendations: "Until further evidence can 
be gathered on possible side-effects or complications from the hepatitis B vaccine, it 
may be worth considering only giving the vaccine to people at high risk, rather than 
to all the population." 
According to Barbara Loe Fisher, "Today, hepatitis B recombinant vaccine used 
in the U.S. is derived from hepatitis B surface antigens produced in yeast cells. A 
portion of the hepatitis B virus gene is cloned into the yeast (a common baker's 
yeast) and the vaccine is produced from cultures of this recombinant yeast strain. 
The vaccine is treated with formaldehyde and contains...hepatitis B virus surface 
antigen...yeast protein [and] aluminum hydroxide...."
[248]The unfortunate reality is that vaccination against hepatitis B has played an 
uncertain role in preventing the spread of the infection in high-risk individuals. In 
fact, the incidence of hepatitis B infection has risen 37 percent since the introduction 
of the vaccine.
[249]
 Despite the evidence of vaccine failure, though, in 1991 the CDC 
recommended universal hepatitis B immunization of infants.
[250]
Though substantial decrease in deaths were shown for various illnesses 
throughout the 20
th
 century, many illnesses still show a significant number of deaths, 
which calls to question what is really causing the decreases in deaths from particular 
illnesses:  For example, Hepatitis A was reduced from 117,333 average deaths in the 
20
th
 century to 24, 291 in 2004.  Similarly, Hepatitis B went from 66, 232 per year 
during the entire 20
th
 century to 17358 in 2004.  What is misleading about the chart 
is that we do not know how many people throughout the 20
th
 century had been 
vaccinated against hepatitis before they died, or that the apparent greater than 70% 
decrease in deaths for both Hep A and Hep B were due to vaccination or other health 
factors.  It is also known that Hep B infection when untreated can cause liver cancer, 
so we may not know the final outcomes for some Hep B related mortality for those 
who were infected in the year 2004, for some time yet.
Health care workers have not rushed to get this injection. A 1990 article in the 
British Medical Journal reports that 86 percent of 598 doctors questioned about 
hepatitis B vaccine believed all general practitioners should receive it, but 309 of 
these doctors had not been vaccinated themselves.
[251]
 In another study, only 25 
percent of nurses and 49 percent of doctors had been immunized, despite the fact 
that 87 percent of the medical staff and 57 percent of the nurses reported a history of 
needle stick injury.
[252]
 And the reaction among family physicians is even less 
enthusiastic: Only 17 percent of 300 family physicians agreed that a 
recommendation of hepatitis B vaccination was warranted for all newborns in their 
practice.
[253]
Is the Hepatitis B Vaccine Safe? As we learn from a study published in the
Pediatric Infectious Diseases Journal, between 1991 and 1994, 12,520 adverse 
reactions to hepatitis B vaccination were reported to the Vaccine Adverse Event 
Reporting System, with 14 percent of these reactions involving newborns and 
infants.
[254]The fact is that the number of reports of complications following hepatitis B 
vaccination is growing steadily. The Association of American Physicians and 
Surgeons (AAPS) reports, "About one-third of the reactions were serious enough to 
result in an emergency room visit or hospitalization, and there were 440 deaths, 
including about 180 attributed to sudden infant death syndrome or SIDS."
[255]
The purpose of vaccinations is to reduce the risks of complications associated 
with the diseases they are designed to prevent. Complications from a vaccine should 
not outweigh those derived from the disease. And yet, according to Dr. Philip Incao, 
who has studied vaccinations and the immune system for three decades, in the case 
of hepatitis B, "...the conclusion is obvious that the risks of hepatitis B vaccination 
far outweigh its benefits."
[256]
Dr. Jane M. Orient, executive director of the Association of American 
Physicians and Surgeons, puts the facts plainly. According to a recent federal 
government study, she says, "children younger than 14 are three times more likely to 
die or suffer adverse reactions after receiving hepatitis B vaccines than to catch the 
disease."
[257]
Is the Hepatitis B Vaccine Effective? Vaccine supporters claim that the 
development of an antibody response to the virus contained in the vaccine equals 
protection against the disease. So we are now vaccinating millions of children 
against hepatitis B to prevent them from contracting the disease later in life. But for 
this to happen, the level of antibodies that are supposed to be protective has to 
remain high for very long periods. The evidence proves that this is not happening.
A study published in the New England Journal of Medicine evaluated the 
persistence of anti-hepatitis-B antibodies in 773 homosexual men immunized against 
the virus. Of these, 635 produced antibodies. After five years, however, such 
antibodies no longer existed in 15 percent of the respondents, and their levels 
declined sharply-below levels deemed to be protective-in another 27 percent. In fact, hepatitis B developed in 55 men, and two individuals became carriers of the hepatitis 
B virus.
[258]
 Another study shows that after three years, 36 percent of individuals 
who initially responded to the hepatitis B immunization lost anti-heptatitis-B 
antibodies.
[259]
Why then are we needlessly vaccinating millions of children if by the time 
they'll be adults and might be exposed to the virus, they won't have the antibodies 
that are supposed to protect them? And, in any case, are these antibodies offering 
protection against the disease?
          Adverse Reactions to Hepatitis B Vaccine. The National Vaccine 
Information Center, in its report on hepatitis B vaccination, cites 38 reports in the 
international medical literature presenting evidence that hepatitis B vaccination is 
causing chronic autoimmune and neurological disease in children and adults. Yet 
this is not information given in the vaccine manufacturer's literature.
Tourbah et al. reported in a 1999 article published in the journal Neurology that 
eight patients developed encephalitis and central nervous system demyelinating 
disease within 10 weeks of receiving hepatitis B vaccination.
[260]
          
FURTHER READINGS: Articles in the medical literature associate the 
hepatitis B vaccine with complications affecting the nervous system
[261], [262], [263], [264]
and the joints
[265], [266], [267], [268], [269]
 as well as other adverse effects.
[270]
Measles/Mumps/Rubella (MMR)Vaccine
As with hepatitis B, physicians are notoriously reluctant to follow their own 
advice when it comes to measles vaccination. One study reported that obstetrician 
gynecologists had the lowest vaccination rate among doctors for the German measles vaccine. Pediatricians didn't fare much better. The authors attributed such 
findings to "fear of unforeseen vaccine reactions."
[271]
The fact that the MMR vaccine is particularly ineffective, with a high 
percentage of those inoculated getting the disease, is undoubtedly a factor here.
[272], 
[273], [274], [275], [276], [277], [278], [279], [280], [281], [282], [283]
According to The New England 
Journal of Medicine, 60 percent of all measles cases among American 
schoolchildren between 1985 and 1986 occurred in those who were vaccinated.
[284]
  
Scientist Trevor Gunn also points out that for several reasons, there is underreporting of illness caused by vaccination.  These include:  financial backlash from 
vaccination producers, and the restricted length of time for which adverse symptoms 
must occur-In England "72 hours for whooping cough and 8-20 hours for the 
MMRP" vaccines.
The Journal of the American Medical Association published a study indicating 
that among 235 cases of student measles reported in Dane County, Wisconsin, in 
1986, more than 96 percent had received a measles vaccine.
[285]
A study reported in 
Morbidity and Mortality Weekly found that 58 percent of 1,600 cases of measles in 
Quebec, Canada, in 1989 occurred in those who had already been vaccinated.
[286]
And the World Health Organization has conceded that those administered the 
measles vaccine have a 14 times greater likelihood of contracting the disease than 
those who remain unvaccinated.
[287]
Jamie Murphy, author of What Every Parent Should Know About Childhood 
Immunization, believes that the vaccine may in fact be causing the illness. "In one 
Chicago study," he says, "90 percent of people vaccinated for measles got measles. 
Another group did not get vaccinated and had a very low percentage of measles." 
Murphy believes that this information should serve as a red flag, causing people to 
realize that vaccines are not working.
[288]
Murphy's observation raises a question that no one has answered: Why are 
people who are vaccinated for these conditions getting them? He thinks the answer 
is that the vaccine does not provide true immunization."The vaccine can never duplicate the kind of immunity that we get from nature. 
Back in the 1950s, when I got the measles and 80 percent of children got either 
measles or mumps...it strengthened your immune system....Also, when a natural 
epidemic of measles occurs, as it does every three to four years in the United States, 
those children who have been vaccinated, because they did not get a true immunity 
from the vaccine, become susceptible to measles."
The CDC states that there has been a resurgence of measles in the United states 
in the past few years, but attributes the problem to the rise in un-vaccinated children.
Murphy argues that rather than preventing measles, the vaccine may simply be 
suppressing it, only to have it manifest as other forms of disease with age.
[289]
 He 
asserts that quite a few diseases are associated with the measles vaccine, including 
"encephalopathies (brain damage), aseptic meningitis, cranial nerve palsy, learning 
disabilities, hyperkinesis and severe mental retardation...."
[290]
          
Results of two separate studies by the Institute of Medicine, one in 1991 and 
another in 1994, showed there to be strong evidence that the MMR vaccine can 
cause acute arthritis, anaphylaxis, thrombocytopenia, and even death.
[291]
Even the package insert accompanying the MMR vaccine says that the vaccine 
may lead to arthritis or arthralgia, either long-term or temporary.
[292]
 Meryl Dorey, 
editor of the Australian publication Vaccination? The Choice is Yours and president 
of the Australian Vaccination Network, points out that the MMR vaccine is also 
associated with Guillain-Barre paralysis, multiple sclerosis, and aseptic meningitis, a 
swelling of the lining of the brain, which can be fatal. "According to Japanese 
studies," she notes, "one in 1,044 children who get this vaccine can get aseptic 
meningitis. It's one of the reasons why Japan withdrew the use of the MMR vaccine 
in 1994."
[293]Viera Scheibner, a retired research scientist, reports that "In April 1993, the 
Ministry of Health and Welfare in Japan decided to discontinue the use of measles, 
mumps, and rubella vaccine (Sawada et al., 1993). This decision was prompted by 
published reports of vaccinated children and their (unvaccinated) contacts 
contracting mumps from the MMR vaccine, and reports of one in 1,044 vaccinees 
developing encephalitis."
[294], [295]
Dorey highlights the problem of shed vaccine virus, noting that it is incorrect to 
say that the MMR vaccine viruses are not infectious. "According to a study 
published in the British Medical Journal, July 4, 1987, immunocompromised 
children should be kept away from MMR vaccinated children for two weeks after 
vaccination due to the...[possible shedding] of the virus.
"These events of infection occur because the vaccines contain live virus 
which can grow in the body and are excreted by the body."
[296], [297]
  The CDC 
tells us that in 1967 the "mumps vaccination was licenced." 
[298]
  However, 22 
years later, in 1989, the Urabe strain of the Mumps virus was removed from 
Canadian vaccines because of a meningitis outbreak. Trevor Gunn cites that 
during this time in the UK:
"cross linking laboratory and hospital reports to vaccination records records, the 
[perceived low risk from meningitis from this particular vaccine] rose to between 1 
in 4000 and 1 in 21,000."
These figures led to the removal of this strain in the UK by 1992.  (From the 
Parliamentary office of Science and technology, "Vaccines and their future role in 
public health, July 1995, and Dawbarns, Solicitors, Kyngs Lynn,  MMR and MR 
Factsheet)Measles Vaccine
A study published in 1994 in the Archives of Internal Medicine evaluated all 
U.S. and Canadian articles reporting measles outbreaks in schools and found that, on 
average, 77 percent of all measles cases in these outbreaks were occurring among 
vaccinated individuals. The authors concluded that "the apparent paradox is that as 
measles immunization rates rise to high levels in a population, measles becomes a 
disease of immunized persons."
[299]
One of the reasons for the resurgence of measles infection is that the antibody 
response to the vaccine virus is only temporary. One study shows that four years 
after MMR vaccination, measles antibodies fall below the putative protective levels 
in 28 percent of children and are no longer present in another 3 percent of 
vaccinees.
[300]
 Experimenting with high-potency vaccines produced even poorer 
results.
[301]
These are just samples of the numerous studies showing that the supposed 
protection offered by the vaccine is short-lasting. By contrast, natural immunity-that 
derived from contracting the disease-is permanent and is transferred from mothers to 
the babies in utero through the placenta. At birth, babies born from mothers who 
have had the disease are protected from the infection during their first year of life by 
the presence of a high concentration of natural antibodies circulating in their blood. 
Measles vaccination, on the other hand, induces lower antibody titers than does 
natural infection. Neutralizing measles antibodies passed by vaccinated women on to 
their newborns disappear rapidly, leaving the babies susceptible to the infection in 
their first year of life, when they are more at risk of complications.
This difference in infants' immunity levels is reflected in a 1995 study 
published in the journal Pediatrics. Researchers found that 71 percent of 9-monthold infants and 95 percent of 12-month-olds had no detectable neutralizing measles 
antibodies in their blood. All infants with detectable measles antibodies at 9 or 12 
months had mothers born before 1963, before the vaccine era.
[302]Measles infection is still a severe disease in adults. A study published in the
American Journal of Medicine in 1993 shows that, of 68 patients over 14 years old 
who developed measles, 33 required hospitalization. Of these, nine were admitted to 
the intensive care unit, six required mechanical ventilation, and two died. The 
authors concluded: "Measles in adults may result in severe, life-threatening 
complications that utilize substantial medical resources. Physicians need to 
appreciate the clinical presentations and manifestations of severe measles in adults 
and to provide measles vaccine to nonimmune adults during community-wide 
outbreaks."
[303]
 Again, immunization has failed to protect children from infection 
and has created a vulnerable population of infants and adults who are at risk of 
developing severe complications. What is the remedy proposed? Again-more 
vaccination!
Another problem found with measles vaccination, documented in several 
studies, is that it produces immune suppression that contributes to an increased 
susceptibility to other infections.
[304]
 One study shows that immunization with live 
measles virus vaccine produces transient immune depression in vaccine 
recipients.
[305]
Trevor Gunn, BSc, wrote an article to the World Health Organization on the 
inadequacies he feels regarding the safety claims made by vaccine administrators 
particularly with regards to measles vaccinations around the world:
[306]
Mr. Gunn felt he was misunderstood in his letter, by the WHO representative 
who responded to him, CJ Clements, saying that Mr. Gunn claimed that vaccines 
provided no safety, when, in fact, Mr. Gunn was only demonstrating the 
shortcomings in the studies that the WHO used to 'prove' effectiveness of vaccines 
when he requested that the World Health Organization prove the effectiveness of 
vaccines before continuing to give them.
First of all, he pointed out that studies on effectiveness use sero-conversion, or 
antibody presence in the blood stream to indicate effectiveness of vaccines.  Mr. 
Gunn points out that the amount of antibody presence the blood does not correlate with the body's ability to fight illness.  Mr Gunn states,  "in the UK the government 
health authority quotes figures of the measles vaccine as being 90% effective."
[307]
Mr. Gunn points out that this does not mean that the vaccine is 90% effective in 
preventing illness, but it means that it produces antibodies in the patients 90% of the 
time.  Mr. Gunn calls for more accurate studies that measure the level of disease 
protection afforded to populations, after they've been inoculated, using cohort groups 
matched for age, population and disease exposure similarities, etc.  A 1991 Press 
Release by the CDC entitled:  Immunization Initiative, praises the benefits of 
immunization and gives a basis for the quoted figure of 90% effectiveness of 
vaccinations mentioned in the above Trevor Gunn article:
The CDC's evidence for "saving countless lives and preventing untold illness 
and suffering" is as follows: First, they cite a figure that before the use of the 
measles vaccine in 1963 , between half and one million people had measles per year, 
from which 500-1000 people succumbed mortally.  We remember here, however, 
David Francis' point that "improved nutrition and public health measures in children 
were more important than medical intervention in 1900", at the height of the measles 
outbreak in America, and although the author claims that measles is making a 
comeback in recent years, he does not give the figures on how he infers that the 
number spiked in the late 1980s as compared to the vaccine's effectiveness in first 
the two decades since its use.
He does state, however, "a number of urban epidemics of measles [happened] 
during 1989 and 1990."  It is important that we examine the numbers of measles 
cases that were reduced, however, after the introduction of the measles vaccine.  
From the Greg Beattie book, "Vaccination A Parent's Dilemma", from 1960-1970, 
the death rate from measles remains essentially flat.  The CDC report, however, 
stated that, "in the last 2 years, 45,000 cases of measles and over 100 deaths 
occurred."  The author cites that, "Almost one-half of all cases have occurred in 
unvaccinated preschool children."  We do not, however, learn in this article, how 
many deaths occurred in the un-vaccinated group.The author seems to be using this figure to bolster his argument that measles 
cases rose as a result of lack of vaccinations.  However, if half of all cases of 
measles occurred in children who were un-vaccinated, then according to his 
reasoning measles should not have occurred in a significant number of children who 
were in fact vaccinated.  Public health officials tend to use the counter intuitive 
claim that the un-vaccinated children provide a contagious health risk to those who 
are in fact vaccinated.  This seems to belie the whole premise that the vaccination is 
supposed to protect the child who has been inoculated.  There seems to be some 
magical thinking with some public health officials regarding the so called, herd 
immunity-that it only works if all or most children are vaccinated.
We note here especially, the two year period following the 1963 introduction of 
the measles vaccine, that David  Francis stated that the childhood decline in 
mortality rate was still, "essentially flat," as noted in our paragraph above.  The CDC 
is proud of the figure that measles deaths were reduced from 4 million per year 
throughout the 20
th
 century to 37 in 2004.
[1]
  Trevor Gunn notes, however, that other 
public health factors play a significant role in outcomes of disease in third world 
countries.
In another report from the WHO on a previously mentioned project in 
Bangladesh, Gunn points out that in one area, the study showed 36% effectiveness, 
and another area showed 46% effectiveness.  This was due, the WHO said, to a local 
epidemic of diarrea which affected the outcome of mortality.  In addition to Mr 
Gunn's assertions, the WHO's defense also points out the weakness of a one -point 
solution to a region where childhood mortality is caused by a host of factors, 
including the main one, (which is lack of nutrition and clean drinking water.)  
Another study, E. Holt, et al from the Journal of Pediatrics, Vol. 85, No 2 
pp188-194, February 1990
[308]
 studied measles outbreaks in a particular area in 
Tahiti.  Although the study was nine months in length as opposed to the 10 months 
in the previous study, it showed greater effectiveness in death reduction than the 
previous Bangladeshi study.  Dr. Gunn suggests that the paper may be manifesting 
the common trait among many vaccine cohort studies that he quotes from the 
Lancet, "gains in survival of a vaccinated group tend to diminish over time to 
approach a survival rate of unvaccinated individuals"
[309]
. (The Lancet April 4, 1981 
765).
Mr. Gunn points out the difficulties with several of the third world studies with 
regards to vaccine effectiveness in measles and other illnesses:  In the study, P. Aby, 
et Al, Pediat Infec DisJ 8: 197-200, 1989
[310]
, Gunn tries to answer whether the measles vaccination would lead to greater or fewer deaths, due to the benefits 
provided by measles in the form of natural immunity in developing countries.  While 
this is a good question ideally, points out Mr. Gunn, the experiment was poorly 
carried out:  Although the study claims that the vaccine prevented 30% of measles 
death, the methods of the paper reveal that the control group was not a nonvaccinated group, but included children who did not sero-convert, and so were 
assumed to have no immune response to the vaccine.  In this case, then, we would 
not know whether deaths in the control group were due directly to the vaccine, due 
to lack of effectiveness of the vaccine, or due to lack of natural immunity provided 
by the measles itself.
In another group of people in this study, 15 out of 123 did not have antibody 
conversion after vaccination, so their results were excluded as well.  Three of this 
group actually died.  In this case, then, we do not know the cause of death of those 
who died, and we still do not find out if those remaining 12 who did not register 
measles antibodies in their blood, were prevented from getting measles at all.
In referring to a paper by Clemens et al, American Journal of Epidemiology, 
Vol 128, No. 6 1330-39
[311]
, Mr. Gunn complains that the cohort group of the study 
was cherry picked for people who did not have a history of measles.  Mr. Gunn 
pointed out that this group may have been less likely to die either from measles in 
general, or may in general be heartier than the people who were selected against in 
the study.
Gunn points out that : "In the UK, over 95% of the mortality had occurred 
before the introduction of the measles vaccine."  In addition, therefore, in a 
developed country, it is difficult to assess the particular role in health prevention 
vaccination plays, because specific tests have not been developed to test vaccination 
related disease prevention.  He also states that it must be important to assess the risks 
of any new medical product administered to the children of an entire population.  He 
points out the hypocrisy of such organizations as the American Academy of 
Pediatrics, whose officials claim that, "the benefits of immunization far outweigh the 
risks," without in reality examining the actual safety of these vaccines.
Gunn points out that there is evidence which links inoculation with illness: The 
Lancet, Vol. 345, April 29, 1995, shows that there is a link between Crohn's Disease 
and the Measles vaccination: the manufacturer's label includes the possible adverse effects:  "fever, rash, coryza, pharyngitis, bronchitis, convulsions, encephalitis, 
thrombocytic purpura, and even death." 
Although some researchers point to good news, "specifically it has been shown 
that children contracting measles were less likely to suffer from allergic conditions 
such as asthma, eczema, and hayfever," (Lancet June 29, 1996)  Gunn also points 
out that infection may cause deleterious effects without the usual measles rash, 
causing, "sebaceous skin diseases, degenerative diseases of bone and cartilage, and 
certain tumours."  He states that the Lancet study, January 5, 1985 suggests that 
interference with the body's own symptomology by repressing measles rash 
symptoms could in fact, interfere with the body's ability to fight the illness 
altogether.  Gunn's rationale for bolstering this idea is the study he mentions from 
the (American Journal of Medicine, Volume 68, pps 344-355, 1980) that people are 
more likely to die from an infection if they are unable to produce a fever in response 
to it.  
Mumps Vaccine
Aseptic meningitis has been epidemiologically associated with receipt of the 
mumps vaccine.
[312]
 In 1989, it was finally determined that it was the strain of virus 
used in the vaccine that caused mumps meningitis. The virus isolated from patients 
who developed meningitis 21 days after injection was identical to that used in the 
vaccine. 
Aypical mumps contracted after receipt of the vaccine is another problem. In 
1980, reports surfaced of atypical mumps in previously vaccinated children, with 
symptoms including fever, appetite loss, nausea, and a generalized rash. The atypical 
mumps occurred when wild natural mumps virus circulated among unvaccinated 
children-a normal event associated with immune system development in humans. 
All the children contracting atypical mumps had been injected with viral vaccine 
five to seven years earlier.Concerning the mumps vaccine's effectiveness, the scenario with mumps is 
very similar to that with measles. There are several studies reporting outbreaks of 
mumps occurring in populations with virtually complete vaccine coverage. Cheek et 
al., for example, writing in the Archives of Pediatric and Adolescent Medicine, 
report a measles outbreak in a highly vaccinated (more than 95 percent) high school 
population. Fifty-three of 54 students who got the disease were vaccinated.
[313]
Another study reported an outbreak of mumps in a Tennessee school with 98 
percent vaccine coverage, where 67 of 68 students who got mumps had been 
previously vaccinated. Thus, mumps cases in this instance were attributed mostly to 
vaccine failure.
[314]
While mumps infection is a largely benign disease when contracted during 
childhood, it becomes more dangerous in older children and adults, who are more 
susceptible to severe neurological, testicular, and ovarian complications from the 
infection. It is alarming to see that vaccination is clearly shifting the occurrence of 
this disease from young children toward those who are older.
[315]
Perhaps the boldest statement on the efficacy of the mumps vaccine in 
preventing the disease comes from the authors of a study conducted in Switzerland. 
They conducted an epidemiological analysis of mumps cases there and found a 
fivefold increase in the number of mumps cases from 1990 to 1993, especially in 
vaccinated children. Among the authors' conclusions was: "The Rubini [mumps] 
strain vaccines, which are the most commonly used in Switzerland, seem to have 
played an important role in the clear increase in mumps cases since 1990."
[316]
Rubella Vaccine
Unfortunately, rubella vaccination is similar to measles and mumps 
immunization in terms of lack of efficacy in preventing the targeted disease. A study 
published in the European Journal of Epidemiology shows that after the Swiss began 
a rubella mass vaccination campaign in 1985, the incidence of rubella remained 
unchanged during the period from 1987 to 1992. The authors concluded: "MMR mass vaccination has not interrupted the circulation of rubella virus in 
Switzerland."
[317]
Also, a study published in the Journal of the American Medical Association in 
1981 shows that 15 years after receiving rubella vaccination, one in 11 children lost 
protection from the vaccine and became susceptible to re-infection.
[318]
 This is 
particularly worrisome because rubella infection is especially dangerous when 
contracted during pregnancy, since the fetus may develop malformations if exposed 
to the virus. Again, the lack of permanent immunity offered by vaccination is 
creating serious problems down the line.
Viera Scheibner has looked in depth into the research on rubella, and informs 
us: "As Cherry (1980) wrote, despite distribution of over 83 million doses of rubella 
vaccine since 1969, there were periodic upswings in incidence. There was also a 
shift in the age groups susceptible to rubella. 'Essentially, we have controlled the 
disease in persons 14 years of age or younger but have given it a free hand in those 
15 or older.' "
[319], [320]
Scheibner adds: "In August 1991, the Institute of Medicine released a report on 
adverse effects of pertussis and rubella vaccines. The evidence indicated a causal 
relationship between RA 27/3 rubella vaccine and acute arthritis in 13 percent to 15 
percent of adult women. Also some individuals were shown to go on to develop 
chronic arthritis."
[321]
FURTHER READINGS: Articles associate the MMR vaccine with adverse 
reactions affecting the nervous system,
[322], [323], [324], [325], [326]
the GI tract,
[327]
 and 
joints.
[328], [329], [330]In Part 3: The smallpox and rotavirus vaccines, provocation diseases associated 
with vaccines, economic, political and legal issues, and the right to refuse 
vaccination.Vaccination: Pain, Profit, and Politics - Part 3
By Gary Null, Ph.D., and Martin Feldman, M.D.
In Parts 1 and 2 of this series, we examined factors countering our beliefs that 
vaccines are safe and effective. We also discussed the effects of specific vaccines, 
including those for diphtheria, pertussis and tetanus, polio, chickenpox, hepatitis B, 
and measles, mumps and rubella. In this final installment, we look at the smallpox 
vaccine, the withdrawn rotavirus vaccine, and the provocation diseases associated 
with vaccines. Finally, we discuss the economic, political and legal issues of 
vaccination, the right to refuse vaccination, and the need to achieve freedom of choice.The Smallpox Vaccine
Smallpox was the impetus for the invention of the vaccine in the New World.  It "was 
introduced into the Americas in the 16
th
 Century and Australia in the 18
th
 Century.  It 
had been present in Africa, Asia and Europe since at least 400 BCE."
[331]
 It was said to 
have traveled along trade routes and to have erupted every ten years.  Variolation, the 
process of sharing a small bit of infected matter with an uninfected person started in 
Africa and was present in Europe in the 18
th
 century.  From the US National library of 
Medicine, "In contrast to Asians and Africans who inoculated by blowing dried 
smallpox scabs up the nose, Europeans and their American cousins tended to inoculate 
through a puncture in the skin."
[332]
  Some, however, died as a result of the procedure, 
and epidemics were also started this way.  It is also widely known that measles 
infections in families were 'gotten through with' by making sure that if one child got 
telltale signs of swollen glands and fever, the other children in the home or the 
neighborhood were invited to share a bedroom, in order to spread the infection and get 
it over all at once.  Even in the late      20
th
 century, well into the 1970's, chickenpox 
was shared in much the same way, allowing children in a family or a neighborhood to 
get through the infection, with the assumption that it could cause greater 
complications as an adult, and that infection would not likely occur twice.  
It was Jenner who first popularized the vaccine program with his smallpox vaccine. A 
close look at history reveals that the procedure never worked, however. Neil Miller, a 
medical research journalist, natural health advocate and author of Immunization 
Theory Vs. Reality: Expos on Vaccinations,
[333]
 summarizes the story, as follows: "In 
1796, Jenner came on the scene saying that when dairy maids caught cowpox they 
could no longer catch smallpox. His medical colleagues disputed his claims, as the 
research of the times indicated numerous cases of dairy maids and other individuals 
catching cowpox and coming down with smallpox. Yet Jenner persisted, and he 
published a treatise on this idea in 1798. He called his treatise Inquiry, and became 
famous for it."
Edward Jenner, a country doctor and a Fellow of the Royal Society formulated the 
idea of vaccines fashioned after the old country tale that those who got cowpox were 
protected from smallpox. In order to test this theory, on May 14, 1796, he removed 
some fluid from Sarah Nelmes' hand which had cow pox lesions, and injected it into 
the arm of James Phipps, who was a healthy eight year old boy. Later, Jenner injected 
the boy with smallpox.
[334]
 When James did not come down with smallpox, Jenner 
concluded "that the cow-pox protectsthe human constitution from the infection of smallpox"
[335]
   He subsequently self-published An Inquiry into the Causes and Effects 
of the Variola Vaccine in June 1798 detailing the James Phipps experiment along with 
other observations. 
Jenner's cowpox vaccine consisted of dry or liquid pus taken from the ulcers of cows 
or humans with cowpox or from the pustules of horses with horse-grease, an infection 
of the heel. Inoculation involved cutting a small hole into the skin and inserting the 
virus from the pus into the arms of the patients with a lancet.  Then Jenner's method of 
transferring a small amount of infected smallpox material from one person to another, 
as we learned earlier, is called variolation, and there were many variations of this 
procedure.
  Critics noted that variolous inoculation, however, could cause bad cases of smallpox, 
so intricate methods were developed to administer it:  Typically, a lancet was used to 
insert variolous material into a small cut of the skin. The variolous matter was taken 
from someone going through the earliest stage of a mild smallpox vesicle growth in 
which there was barely any fluid. This material was then inserted into one patient. 
Subsequently when mild symptoms occurred, new material was taken from that 
patient and then used on other patients. The process of collecting variolous matter was 
continued from arm to arm.
[336]
 A smallpox epidemic in France revealed that the 
inoculation failed badly to protect the patients of Dr. Gatti in France. As a result, Paris 
outlawed these inoculation practices. 
[337]
Jenner, however, espoused a milder technique of variolation: "I have the strongest 
reason for supposing that if either the punctures or incisions be made so deep as to go 
through it and wound the adipose membrane, that the risk of bringing on a violent 
disease is greatly increased. I have known an inoculator whose practice was to cut 
deep enough (to use his own expression) to see a bit of fat," and there to lodge the 
matter. The great number of bad cases, independent of inflammations and abscesses 
on the arms, and the fatality, which attended this practice, was almost inconceivable; 
and I cannot account for it on any other principle than that of the matter being placed 
in this situation instead of the skin. It was the doctor's practice to make as slight an 
incision as possible upon the skin, and there to lodge a thread saturated with the 
variolous matter... it has been proved that variolous matter, when much diluted with 
water and applied to the skin in the usual manner, will produce the disease." 
Creighton, a 19
th
 century historian put it this way, "The matter for inoculation was not 
taken from a natural or accidental eruption of smallpox; it was taken from the local 
pustule alone of an artificial inoculation, and it was taken from the very earliest period 
of the local pustule at which any fluid could be got at all, or "just before the 
commencement of the eruptive fever."
[338]Critics of variolation cite that over scrupulous variolators could actually fail to give 
any inoculation at all: By that means, as [Salmade], a French variolator of the time 
reports, " the smallpox becomes at length weakened to the point of nullity, so that the 
last inoculations are without effect."
[339]
  Thus, weakened variolation might not cause 
any illness, but it also might not engender any immunity, either.
[340]
Jenner's early efforts to coerce his colleagues to his way of thinking were 
"ineffectual; his brethren were acquainted with the rumor, but they looked upon it as 
one of those vague notions from which no accurate or valuable information could be 
gathered, especially as most of them had met with cases in which those who were 
supposed to have had cowpox had subsequently been affected with smallpox."
[341]
Creighton added, "Certainly for those who knew by inspection what the pox of the 
cows' teats was, and most of all for those who had suffered the painful and often 
obdurate ulcers on their own hands, there would be no suggestion of real likeness to 
smallpox, or of the one disease being in any way related to the other. It was the jingle 
of the names that brought the two together in the first instance."
[342]
 The "diseases 
themselves were totally unlike. It was just because Jenner had no profound sense of 
these empirical realities that he went blundering into visionary nonsense in the first 
instance, and at length into systematic mystification and chicane[ry]."
[343]
  "In the monograph by Nicholas Massa, of Venice, he says they [smallpox pustules] 
occurred over the whole body-on the limbs, on the face and head, and amongst the 
roots of the hair. In his particular description we find such terms as elevated, tumid, 
moist; red, livid, whitish; small, dry, itching ; broad, flat, soft. They came out 
comparatively early in the disease (second or third week even), and their outbreak was 
often the signal for the notorious pains in the head and limbs to abate."
[344]
  Cowpox, on the other hand, was the ulcerous pox of the cows' teats, which can infest 
the skin, namely the hands, of those who milk the cows. Those infected will also feel a 
flu-like illness often accompanied with swollen and painful glands in the armpits. 
Horse-grease, another illness which Jenner conflated into his smallpox theory affected 
the hocks of horses causing inflammation and swelling.  Contact with the diseased 
heels created an infection with burning white blisters which later become painful 
corroding ulcers.
[345]
  Clayton, a veterinarian in Jenner's county spoke of the separate nature of horse 
grease from cowpox:  He wrote that he was "extensively employed, particularly in 
curing the [horse-]grease" and also elaborated that "the grease is most prevalent in the 
winter, at which time he has never known the cowpox to occur... [also] he could not recollect ever to have had horses with the grease and cows with the cowpox under 
care at the same farm... [Furthermore] he is very certain he has frequently had cows 
with the cowpox, where no horses whatever have been kept."
[346]
 However, Jenner did 
not see it that way. In the opening of the first chapter of his Inquiry, he wrote that 
horse-grease "is an inflammation and swelling in the heel, from which issues matter 
possessing properties of a very peculiar kind, which seems capable of generating a 
disease in the human body,...which bears so strong a resemblance to the smallpox that 
I think it highly probable it may be the source of the disease.
Jenner's Inquiry paved the way for universal acceptance of vaccination as a gold 
standard of modern medicine's ability to protect us from disease. Jenner's previous 
"medical papers" however, were spurious. Previous to his papers on cow-pox, one was 
on the subject of preparing a tartar emetic, and an another was on the observation of 
calcified coronary arteries of the heart in a case of someone who suffered from angina 
pectoris. His "philosophical papers " are represented solely as observations on the 
cuckoo, in the Philosophical Transactions for 1788." 
[347]
 It was this paper on the 
cuckoo, which was essentially a piece of fantasy,  that propelled Jenner into the Royal 
Society which was chaired at that time by Sir Joseph Banks, a friend of Jenner's, a 
year later.
[348]
Jenner's Inquiry paper involved about 2 years of research and one single experiment 
involving cowpox and smallpox inoculations on the one patient, James Phipps. His 
status as a fellow of the Royal Society and his strength as a salesman were the reasons 
for his success in twisting myth into science. Dr. Baron, Jenner's own biographer, 
wrote that Jenner frequently mentioned cowpox innoculation immunity to smallpox in 
the meeting at the Society which involved Fewster of Thornbury, the chief authority 
on cow-pox. 
Dr. Charles Creighton M.A. M.D, professor of Microscopic Anatomy at Cambridge, 
wrote the section on 'Vaccination' in the ninth edition of the Encyclopedia Britannica, 
published in 1888. A year later, he also wrote JENNER AND VACCINATION - A 
Strange Chapter of Medical History, a detailed history of Edward Jenner's 
professional life.  Creighton stressed that one danger in using variolous inoculation as 
a measuring stick for smallpox infection was that the cowpox vaccine 
"caused a swelling and obstruction of the absorbent glands in the armpit and neck, and 
to that extent made them incapable for the time, and in some cases for long after, of 
taking up and passing into the lymphatic circulation another virus inoculated under the 
skin at the same place... Apart from the swollen and clogged state of the absorbent glands after cowpox [inoculation], the mere presence of a sore of any kind on the arm 
served to divert and obviate the full action of a new infection"
[349]
Many of the children used as test subjects were from poor households, orphanages and 
foundling hospitals. These children often have chronic swelling of the lymphatic 
glands. Even Jenner noticed the tendency to resist variolous inoculation.  He said in 
his Inquiry, "There are many who, from some peculiarity in the habit, resist the 
common effects of variolous matter inserted into the skin."
[350]
He did not mention who 
these people are, nor did he feel the need to stop using the variolous test as barometer 
for smallpox immunity since he discovered some people are immune to the variolous 
test. 
James Phipps, living proof of Jenner's smallpox immunity, very likely fell into this 
category. After writing the Inquiry, Jenner noted that James "has been very unwell 
lately, I am afraid that he got tubercles in the lungs. He was recently inoculated for the 
smallpox... for the twentieth time, all without effect."
[351]
 Being a test subject with 
numerous cowpox and variolous inoculations and having tubercles in the lungs are 
signs that James Phipps likely had swollen lymphatic glands too. Creighton elaborates 
in that "an eruption after cowpox has the same significance as an eruption after the 
pox proper; it is a secondary effect, or a sign that the constitution has been touched by 
the infection. A person still under the influence of the secondaries of cowpox would 
not be a likely subject for smallpox engrafted on the top of it... [Furthermore,] the 
mere presence on the skin of spots or pimples or vesicles or blebs would hinder the 
full evolution of smallpox by inoculation... The presence of any common eruption, 
even itch, was well known to prevent the cowpox itself from taking. Jenner began, 
about the year 1804, to explain the failure of cowpox by an ambitious doctrine of 
"herpes"... it had this grain of truth in it, that an infection inserted under the skin 
would not have a fair chance of being absorbed if the skin were already engaged with 
an eruption even of the most ordinary kind. In so far as that was a plea for the failure 
of cowpox, it was a plea for the failure of inoculated smallpox." 
[352]
Ironically, the variolous inoculation was later used as one of the many excuses for 
cowpox vaccine failure and subsequently played a part in creating the first English 
mandatory vaccination program in 1853. The idea is that variolous inoculations were, 
in addition to causing the smallpox revival, encouraged people to ignore the 'true 
protector', cowpox vaccine. In 1840, England, spurred on by the Medical Society, 
passed a law to protect the public from variolous inoculation under penalty of 
imprisonment. The strict penalty was made by Mr. Wakley, editor of The Lancet.  He 
blamed variolous inoculation for 17,000 smallpox deaths in one year, and he also added that smallpox would disappear if variolations were prevented and vaccination 
adopted.
[353]
There was, however a general revival of variolous inoculations over cowpox 
vaccination. Despite the fact that the public had 40 years of Jenner's vaccination, 
smallpox was still a continuous plague. Creighton wrote, 
"In the disastrous epidemic among children at Norwich in 1819, ...due to overcrowding of the town by a great influx of families from the country while trade was 
brisk, the failures of vaccination were so obvious to those directly concerned that the 
common people insisted on having their children inoculated in the old way to save 
them from the contagion."
[354]
In 1853, the Compulsory Vaccination Act was instituted, mandating vaccination for 
children. Built on the precedent of the law that made variolation illegal in Great 
Britain in 1840, the new idea, propagated by the Vaccination Committee, was that 
preventing smallpox required the cowpox vaccine.
[355]
Yet despite the vaccinations, from 1857 to 1859, the smallpox epidemic killed 14,244 
people. From 1863 to 1865, a second outbreak claimed 20,059 lives. A more stringent 
compulsory vaccination law was passed in 1867, and those who evaded inoculation 
were prosecuted. An intensive four-year effort to vaccinate all people between the 
ages of 2 and 50 resulted in 97.5 percent of the population being vaccinated. The 
following year, though, England experienced its worst-ever smallpox epidemic; 
44,840 lives were lost. Overall, from 1871 to 1880, during this period of compulsory 
vaccination, the death rate from smallpox leapt from 28 to 46 per 100,000.
The early years of the 19th century in Europe saw a noticeable reduction of the 
epidemic outbreaks of the all disease including smallpox. This fact gave ammunition 
to the vaccine establishment. In 1904, Dr. Charles Ruata, M.D. pointed out the 
specifics in the rise and fall of diseases in England in the period before and after the 
turn of the 19
th
 century. Using data from the Reports of the Royal Commission, who 
have a pro-vaccination view, and from the annual reports of the Registrar-General, he 
made twelve charts, "each showing the comparative rise or fall of small-pox mortality 
and other diseases in various places and under different conditions; and all these 
without exception demonstrate either that vaccination has no effect whatever, or that it 
tends to increase rather than decrease small-pox mortality."
[356]
 His smallpox diagram 
of London shows that the disease "decreased during the ten years before vaccination at 
very nearly the same rate as it did in the ten years after vaccination...General mortality 
also decreased after 1800 more rapidly than before 1800. Yet the Royal Commissioners declare that there was nothing but vaccination to produce the decrease 
of small-pox, and that there was no improvement in sanitation in the beginning of the 
nineteenth century, as compared with the latter part of the eighteenth century, to 
account for the difference."
[357]
Ruata cited five primary reasons for the decline of most diseases in London after the 
1700's. First, diseases, especially during epidemics, are much higher in cities. Many 
city dwellers moved to newly built "West-end squares and suburbs." Secondly, 
sanitation on the streets was improved, while the roads were better maintained. That 
lead to the third reason; better roads allowed more fresh meat, vegetables and milk to 
be brought into the city, which gave the inhabitants better nutrition. The fourth reason 
was an improved water supply. Finally, the dead were not rotting in the city anymore 
as cemeteries were built outside London while many city graveyards were 
permanently closed. He added that these results strikingly decreased, "the death-rate in 
a number of the most fatal diseases (as recorded in a Table by Dr. Farr, reprinted in 
the Third Report of the Royal Commission) to fully one-half in 1801-10 as compared 
with 1771-80; an amount of improvement which has never occurred in any similar 
period during the whole of the 270 years for which we have official statistics."
[358]
          One of the greatest smallpox epidemics in Europe happened between 1870 and 
1872. By this time, cowpox vaccination was established with many countries adopting 
mandatory vaccination in at least some form. In German Prussia the official death 
count was 124, 948. No records were kept for the vaccinated or unvaccinated although 
there was some evidence that the vaccinated were at least comparable to the 
unvaccinated.
[359]
 In England and Wales, the official registration report showed 42,210 
deaths from 1871 to 1872. This is a staggering figure considering the fact that England 
established a mandatory children's vaccination program in 1853 under the strict 
penalty of imprisonment for violators.
[360]
  
Leicester, a manufacturing town in England with 200,000 inhabitants, offers us a great 
insight into the nature of cowpox vaccination. Having suffered greatly in previous 
epidemics, Leicester was one of the most completely vaccinated towns in all of 
England up to 1872. According to Ruata, in 1871, the "small-pox deaths during that 
year...[were] more than 3,500 per million of the population, or about one thousand per 
million more than the mortality in London during the same epidemic. Here an almost 
completely vaccinated community suffered more than unvaccinated and terribly 
unsanitary London, on the average of the last forty years of the eighteenth century." 
After their horrible experiences, Leicesterians refused vaccination even under the 
threat of imprisonment. By 1890, their ratio of vaccinated versus unvaccinated was 
reversed to only 5 percent vaccinated. Doctors scolded them: "that once small-pox was introduced it would run through the town like wildfire and decimate the 
population. Yet it has been introduced again and again, but it has never spread; and 
from that day to this [1904], no town in the kingdom of approximately equal 
population has had such a very low small-pox mortality as this almost completely 
unvaccinated and--as the doctors say--unprotected population!"
[361]
Modern smallpox vaccinations include the following ingredients: " live vaccinia virus, 
with 'some microbial contaminants,' according to the Working Group on Civilian 
Biodefense, polymyxcin B sulfate, streptomycin sulfate, chlortetracycline 
hydrochloride, and neomycin sulfate, glycerin, and phenol -a compound obtained by 
distillation of coal tar, and vesicle fluid from calf skins."
[362]
The CDC website admits that the smallpox vaccine is not made from smallpox virus: 
"The vaccinia virus is the 'live virus' used in the smallpox vaccine. It is a 'pox'-type 
virus related to smallpox. When given to humans as a vaccine, it helps the body to 
develop immunity to smallpox. The smallpox vaccine does not contain the smallpox 
virus and it cannot cause smallpox."
[363]
 Juniors at Stanford University, Jennifer 
Aguayo and Jessica Caldern, write, "Vaccinia virus is a big mystery in virology. It is 
not known whether vaccinia virus is the product of genetic recombination, or if it is a 
species derived from cowpox virus or variola virus by prolonged serial passage, or if it 
is the living representative of a now extinct virus."  The university of Florida College 
of medicine information page writes something similar: "Vaccinia is the virus that was 
used for vaccination against smallpox. Its exact origin is unknown, however, as it does 
not appear to be related to any other known pox virus. Some people think that it is a 
recombinant of smallpox and cowpox, while others think that it may be a derivative of 
horsepox, a virus that no longer exists (if it ever did)."
Historians cite improvements in America in the 20
th
 century to the smallpox vaccine 
which included the pedal injection system for mass injections, a special 'bifurcated 
needle' in 1961 that penetrated the skin twice in one injection, and the all out mass 
eradication effort, called E2  which was considered to have wiped out smallpox on a 
grand scale in Sierra Leone.
[364]
  The CDC notes that smallpox was reduced from an 
average of 29,005 deaths per year during the 20
th
 century to 0 cases on 2004.  In 1971 
the CDC states that "small pox vaccination was ended in the United States." 
[365]
Despite this fact, in 2001 as a result of terrorist threats, "the United States established 
a plan to reintroduce Smallpox vaccine if necessary."
[366]
Edward Jenner is indeed a man who changed the world. The current history displays a 
Renaissance man of great integrity, but with the bogus variolous tests and cries of 
spurious cowpox, Jenner managed to create a myth of smallpox immunity from his cowpox vaccines. That myth became a Teflon medical dogma. In spite of the 
overwhelming evidence of cowpox vaccination failures during the many smallpox 
epidemics, vaccination was still propped up as a gold standard of medicine by an 
industry that would not let it die. The result of the vaccine establishment's tenacity is 
the resurgence of the boast that vaccination eliminated smallpox today. A vaccine is 
created only for one purpose and one alone; that is to provide immunity to the 
vaccinated from the attack of the single disease that it was made to defend against. If 
cowpox vaccine works, there should not even be one death from smallpox in the 
vaccinated. Jenner stated in his Inquiry, unequivocally, "that the person who has been 
thus affected [by vaccination] is forever after secure from the infection of the 
smallpox." The number of smallpox deaths in the vaccinated in the past 200 years is 
also unequivocal; truthfulness aside. Proper hygiene, sanitation and better living 
conditions are the true conquerors of smallpox.
Rotavirus Vaccine  Rotavirus is a common virus that usually causes mild and selflimiting diarrhea in children. In 1998 Wyeth Laboratories, Inc., of American Home 
Products, released RotaShield, a new vaccine against the infection. Since four major 
types of rotavirus cause disease in humans, the vaccine was tetravalent, consisting of 
genes from four viral strains. 
The Advisory Committee on Immunization Practices (ACIP), American Academy of 
Pediatrics (AAP) and American Academy of Family Physicians (AAFP) 
recommended universal use of RotaShield for healthy infants at 2, 4, and 6 months of 
age. (Although the AAFP had been in favor of voluntary vaccination or vaccination of 
high-risk infants only, the ACIP had wanted the universal recommendation.) A year 
later, though, the vaccine was removed 
from the market after 99 cases of bowel intussusception-a bowel obstruction in which 
one segment of the intestine telescopes inwardly into another-and two deaths were 
reported to the Vaccine Adverse Event Reporting System.
Bowel intussusception is a severe condition that often requires surgical intervention 
and can lead to death in the absence of prompt treatment. For example, of the first 15 
reported infants who developed bowel intussusception, eight had to have surgical 
reduction, including one infant who had 7 inches of intestine removed. (1) These 15 cases, it should be noted, constituted but a small fraction of the actual number of 
intussusception cases caused by RRV-TV, as the new vaccine was called. According 
to the Morbidity and Mortality Weekly Report of July 16, 1999, "because reporting to 
VAERS of adverse events following vaccination is incomplete, the actual number of 
intussusception cases among RRV-TV recipients may be substantially greater than 
that reported."
[367], [368]
 And so it was. As soon as the Centers for Disease Control and 
Prevention (CDC) began warning doctors about the possibility of this complication, 
cases of bowel intussusception started being reported around the country. This is yet 
another important example of how vaccine complications, unless specifically looked 
for, go unnoticed by the medical community and thus by society at large.
After it was approved, an estimated 1 million U.S. infants were vaccinated with 
RotaShield. What is even worse about the history of the rotavirus vaccine is not only 
the fact that it caused the hospitalization and deaths of several children, but the fact 
that prelicensure trials had already demonstrated that it caused bowel intussusception 
at rates 30 times higher than those expected. This is what emerged from analysis of 
prelicensure trial data by the Association of American Physicians and Surgeons 
(AAPS).
[369]
Is the Approval Process Tainted? So here is the question: If the fact that the vaccine 
could cause a potentially lethal complication was already known, why did the FDA 
approve it? Why had nobody warned doctors to watch for this complication? Indeed, 
these and more questions prompted the AAPS to request a Congressional investigation 
of the vaccine approval process. 
As Dr. Jane Orient, executive director of the AAPS, writes in a letter to 
Representative Dan Burton, "The situation with the rotavirus vaccine may be a clue to 
a far more serious problem with the vaccine approval process."
Dr. Orient makes the important point that "Decisions about vaccines given to children 
should be made by parents in consultation with the child's attending physician, not 
mandated by a small group of 'experts' with minimal accountability."
[370]Lessons of History
As we've seen again and again, there has been a direct relationship between 
vaccinations and an increased incidence of the diseases they supposedly prevent. This 
contradiction has prompted several researchers to conclude that vaccines are neither 
safe nor effective.
          
In a 1926 British Medical Journal article, a Dr. Parry asks why vaccine statistics 
reveal a higher death rate among the vaccinated: "How is it that smallpox is five times 
as likely to be fatal in the vaccinated as in the unvaccinated? How is it that in some of 
our best vaccinated towns, for example, Bombay and Calcutta, smallpox is rife, while 
in some of our worst vaccinated towns, such as Leicester, it is almost unknown? How 
is it that something like 80 percent of the cases admitted into the smallpox hospitals 
have been vaccinated, while only 20 percent have not been vaccinated? How is it that 
in Germany, the best vaccinated country in the world, there are more deaths in 
proportion to the population than in England? For example, 28 deaths in England in 
1919 per 100,000, and 707 in Germany? What is the explanation?"
[371]
Tuberculosis. Trevor Gunn makes the point that "Improvements in living standards 
have almost as much an effect on reducing mortality as that predicted vaccination." 
Mr. Gunn responded to the allegations by the World Health Organization that double 
blind studies were unethical because they limit the control group from receiving the 
benefits of life saving immunity. First of all, he pointed out that double blind placebo 
controlled trials of tuberculosis vaccine were initiated after some children died after 
receiving inoculations from a contaminated batch of vaccines.  The results of the 
double blind study showed no increase in immunity from receiving the vaccination, 
and possible increase in actual tuberculosis cases for the cohort that did in fact receive 
the inocculations. Despite this fact, Gunn says the vaccine has continued to be used.  
Gunn also points out other flaws in the tuberculosis studies, which he feels ought to be 
taken into account in all studies on vaccination effectiveness:
1)That there were not standards for diagnosis, so that before and after comparisons of 
illness were not accurate.2)Studies did not take into account the importance of public health factors when 
examining illness related causes.
          
In addition, those who take issue with universal immunization programs point out that 
the programs don't discriminate between children who may benefit from a certain 
vaccine and those who might be hurt by it. Babies are given blanket immunization 
regardless of their previous or current state of health and regardless of their varying 
susceptibilities to side effects. Ideally, there should be a much more selective 
vaccination system, with parents given complete information so they can make up 
their own minds as to whether the risks associated with a particular procedure 
outweigh its potential benefits. Just as different races are known to suffer 
disproportionately from various allergies and food sensitivities, studies also indicate 
that they may experience different reactions to vaccines.
Provocation Disease
One of the most hazardous and insidious effects of vaccination lies in its potential to 
induce other forms of disease, a phenomenon known as provocation disease.
[372], [373], 
[374], [375], [376], [377]
 The mechanisms that cause this to happen are unclear, although 
many scientists believe that latent viruses-those already existing within a person-may 
be stimulated by vaccinations, and that this may be enough to activate a particular 
illness. Vaccination, therefore, may not be the sole cause but rather the final trigger 
for an illness.
In his book Vaccination and Immunization: Dangers, Delusions & Alternatives,
[378]
Leon Chaitow states that there is no way of knowing when such latent or incubating 
situations may be operating, and therefore no way of knowing when a vaccination 
may produce this sort of provocation.
[379]
 He goes on to warn that provocation of a 
latent virus is a potentially dangerous possibility with every vaccination procedure.Many diseases thought to be caused at least partially by vaccinations do not surface 
until years later, by which time it is difficult to prove a connection. Some of the 
relationships between vaccines and the specific conditions they provoke are discussed 
below.
Allergies. According to Dr. Harris Coulter, co-author of A Shot in the Dark
[380]
 and 
author of Vaccinations, Social Violence, and Criminality, among other experts,
[381]
says that vaccines and allergies are clearly connected. "What does allergy mean? It 
means that your body is ready to react very, very quickly when exposed a second time 
to a substance to which it is allergic. If you are allergic to ragweed, [a small amount] 
of ragweed will start you sneezing. Now, if you vaccinate a person against pertussis or 
some other bacillus, you are making that person allergic to that bacillus. That's what 
being vaccinated actually means. It means you are allergic to that bacillus, in the sense 
that your body will react very, very rapidly if exposed to that bacillus a second time."
Sudden Infant Death Syndrome (SIDS). Sadly, many studies have shown 
vaccination to be a cause of sudden infant death syndrome. Reports Alan Phillips, 
founding director of Citizens for Healthcare Freedom, Durham, N.C.: "One study 
found the peak incidence of SIDS occurred at the ages of 2 and 4 months in the U.S., 
precisely when the first two routine immunizations are given, while another found a 
clear pattern of correlation extending three weeks after immunization. Another study 
found that 3,000 children die within four days of vaccination each year in the U.S. 
(amazingly, the authors reported no SIDS/vaccine relationship), while yet another 
researcher's studies led to the conclusion that half of SIDS cases-that would be 2,500 
to 5,000 infant deaths in the U.S. each year-are caused by vaccines."
[382], [383], [384], [385]
          
According to Viera Scheibner, a retired research scientist, "Baraff et al. (1983) 
investigated 145 SIDS victims who died in Los Angeles County between January 
1979 and August 1980: Fifty-three of these babies had received a DPT immunization, 
27 within 28 days of death. Six deaths occurred within 24 hours and 17 occurred 
within 1 week of DPT immunization. These sudden infant deaths were 'significantly 
more than expected were there no association between DPT immunization and SIDS.' 
"
[386], [387]Immunosuppression and Autoimmune Disease. The body needs to experience a full 
inflammatory response to create immunity, and vaccines do not allow this to happen. 
Instead, a chronic condition is created that can set the stage for autoimmune disease.
In Immunization: The Reality Behind the Myth, author Walene James describes the 
mechanics involved in vaccines inducing autoimmune disorders: "Live viruses, the 
primary antigenic material of [some] vaccines, are capable of surviving or remaining 
latent in the host cell for years, without provoking acute disease."
[388]
          
Cynthia Cournoyer, author of What About Immunizations?, believes that a key 
principle involved in understanding the many negative effects of vaccines is the fact 
that the immune system can only tolerate so many challenges, especially before it is 
given a chance to develop to maturity. 
"Every child," she writes, "is born with a finite ability to combat disease. This is his 
total immune capacity. Once a child experiences a particular disease, permanent 
immunity is extremely efficient, using probably 3 percent to 7 percent of the total 
immune capacity of an individual. In the case of routine childhood vaccination, it is 
likely that as much as 30 percent to 70 percent of total immune capacity becomes 
committed.
          
"These findings could indicate that a child's immunological reserves are substantially 
reduced due to standard vaccine programs. Far from producing a genuine immunity, a 
vaccine may actually interfere with or suppress the immune response as a whole, in 
much the same way that radiation, chemotherapy and corticosteroids and other antiinflammatory drugs do."
[389], [390], [391]
          
Cournoyer continues, "Although the body will not make antibodies against its own 
tissues, viruses becoming part of the genetic make-up may cause cells to appear 
foreign to the immune system, making them a fair target for antibody production....          
"Under proper conditions these latent pro viruses could become activated and cause a 
variety of diseases, including rheumatoid arthritis, multiple sclerosis, lupus 
erythematosus...and cancer."
[392]
Activists Speak Out on Vaccine Dangers
Barbara Loe Fisher, cofounder and president of the National Vaccine 
Information Center (NVIC), Vienna, Va., has advocated the right of individuals 
to make informed, independent vaccination decisions for themselves and their 
children for two decades. She shares her concerns about a number of issues, as 
do some of her colleagues engaged in the fight against government-mandated 
vaccines.
Problems with Temporary Immunity and Benefits of Childhood Disease. 
Vaccines provide only temporary immunity, whereas when you get the natural disease 
you have permanent immunity most of the time. Viera Scheibner writes that 
"generations of children with this inadequate immunity would grow into adults with 
no placental immunity to pass on to their children, who would then contract measles at 
an age when babies are normally protected by maternal antibody....
          
"Perhaps the most unfortunate thing about the idea of eliminating infectious diseases 
by vaccination is that indeed there is no need to do so. As pointed out by the group of 
Swiss doctors opposing the U.S.-inspired policy of mass vaccination against measles, 
mumps and rubella in Switzerland, 'We have lost the common sense and the wisdom 
that used to prevail in the approach to childhood diseases. Too often, instead of 
reinforcing the organism's defenses, fever and symptoms are relentlessly suppressed. 
This is not always without consequences...' "
[393], [394], [395]
          Lastly, Scheibner states, "There is no need to artificially immunize our children and 
ourselves. The body has proper, natural mechanisms to create immunity to diseases. 
The diseases themselves are the priming and challenging mechanisms of the 
maturation process leading to the competence of the immune system....
[396]
The EZ Measles Medical Fiasco. In the mid-1980s researchers from the CDC and 
Johns Hopkins University started vaccinating babies as young as 4 months old with 
the experimental high-titer Edmonston-Zagreb (EZ) measles vaccine. Targets were 
more than 1,500 black and Hispanic babies in Los Angeles and thousands of babies in 
several Third World countries. The experiment was halted in 1991, after results of 
several studies showed that female babies receiving the high-potency vaccine had a 95 
percent increased mortality rate compared to those injected with the standard measles 
vaccine.
[397], [398]
Economic, Political, and Legal Issues
Cynthia Cournoyer has noted that vaccines are the only products in the U.S. that are 
legally mandated to be used by every person born.
[399]
Barbara Loe Fisher paints an ominous picture of things to come: "As consumers, we 
can bring very little economic pressure on the system to have that product improved or 
removed, because all of us are required by law to use it. It's a dream for the 
pharmaceutical industry involved in making vaccines, because there's no way anybody 
can say no. It's a stable, ready-made market, and the enactment of the compensation 
law in 1986 has removed almost all liability for drug companies....
"What concerns us most is that there is an electronic monitoring system being put in 
place by state public health departments with federal funding-they're trying to get it in 
every child born and monitor his or her vaccination status....
          "...If we don't act now, the public health infrastructure is going to get more power to 
intrude in our lives, intrude in our health care choices. It all comes down to whether or 
not we, as individuals, are going to fight for the right to make informed health care 
choices, including vaccination choices, for ourselves and our children, and whether we 
are going to hold the drug companies and government health officials accountable for 
the injuries, deaths, and chronic illnesses caused by vaccines they produce, sell, and 
promote for mass use."
[400]
          
One interesting financial aspect of vaccines involves the federal ACT Compensation 
Program. An excise tax of $23.50 was tacked onto the price of vaccines in 1988 to 
fund this compensation program. What this means is that consumers are footing the 
bill for any injuries or deaths that may result from medical procedures that they are 
required by law to undergo.
[401], [402], [403]
          
Alan Phillips notes: "[Pharmaceutical companies] have been allowed to use gag orders 
as a leverage tool in vaccine damage legal settlements to prevent disclosure of 
information to the public about vaccination dangers. Such arrangements are clearly 
unethical; they force a nonconsenting American public to pay for vaccine 
manufacturers' liabilities, while attempting to ensure that this same public will remain 
ignorant of the dangers of their products."
[404], [405]
          
Vaccine critic Randall Neustaedter concurs: "Profit has always been the goal of 
vaccine manufacturers. When lawsuits leveled at drug companies began wiping out 
profits gleaned from the pertussis vaccine, the manufacturers simply stopped 
production of the vaccine. The United States government stepped in to pay these 
vaccine-damage claims. Only then did the drug companies agree to resume vaccine 
production...."
[406]
Right to Refuse Vaccination
A question frequently asked of advocates on the front lines of the freedom-fromvaccines movement concerns legal rights of refusal. According to Fisher, whose book 
The Consumer's Guide to Childhood Vaccines provides information on this topic, "It is common for hospital and clinic or emergency room staff to ask you about your 
child's vaccination status. You don't have to provide them with written proof. A verbal 
answer is satisfactory. However, if you are being questioned closely and feel that you 
are being pressured into vaccinating your sick child without your consent, you should 
understand that you have the right to refuse to give permission to have your sick child 
vaccinated if you believe vaccination at the time will endanger your child's health or 
life. You may choose to reassure medical personnel that you will consult a private 
pediatrician for further guidance about vaccination."
[407]
          
One special precaution, Fisher notes, involves pregnant women. "When pregnant 
women are admitted to a hospital to have a baby, many times while in active labor, the 
hospital will require that the mother or father sign a paper agreeing to have the baby 
treated by medical personnel while in the hospital. Signing this paper may also 
constitute your consent to having your newborn vaccinated with hepatitis B vaccine 
shortly after birth. Many parents have reported that their newborns are being 
vaccinated without their knowledge and, when they ask why, they are told they signed 
a consent form prior to admission agreeing to medical treatment the hospital 
determined was necessary. Read any consent form you sign carefully. If you do not 
want your newborn vaccinated shortly after birth, you have the right to sign it after 
writing in an exception, such as, 'I do not consent to have my child given any 
vaccinations prior to discharge from the hospital.' Bring this to the attention of the 
person admitting you and the nursery supervisor and ask to have it printed on the 
outside of your chart. Some parents take the extra precaution of not leaving the 
newborn alone with hospital personnel without being able to observe the baby."
[408]
          
In the unfortunate case of an adverse vaccine reaction resulting in medical bills 
totaling more than $1,000 or injuries lasting longer than six months, parents qualify 
for benefits under the National Childhood Vaccine Injury Act of 1986 (PL 99-
660).
[409]
 Through fiscal year 2001, the National Vaccine Injury Compensation 
Program had paid $1.3 billion in total awards (petitioner's awards and attorney's fees) 
for approximately 1,660 compensable petitions.
[410]
What the Future May HoldFisher believes that if we are concerned about our health and our freedoms, we should 
be worrying about the future. "I truly believe that unless the public wakes up to what 
is happening, and starts standing up for their right to be fully informed about vaccines, 
and their right to make informed independent vaccine decisions, the day will come 
when we won't have that right. We will be forcibly vaccinated by law without 
exception."
[411]
  
Fisher urges everyone to stop being complacent, to start becoming informed about 
vaccines and diseases and to act. Specifically, she states, "You are going to have to 
work to amend your state's laws. If you would like to be better informed and to help 
get the truth out, please join our grassroots vaccine safety movement."
Holistic Health and Freedom of Choice
Fisher adds, "The alternative health care movement in this country is going to play a 
vital role in the vaccine safety movement.
[412]
 Those who are looking into chiropractic, 
osteopathic medicine, naturopathic, homeopathic, vitamin therapy, etc., are looking 
for ways to boost the immune system through more natural means in order to be able 
to naturally deal with viruses and bacteria that they come in contact with. This is a 
very important movement."
Dr. Dean Black, author of Immunizations: Compulsion or Choice, agrees. He sees 
vaccinations as only a shortcut for those people in our society who have not taken full 
responsibility for their health. 
"It's a way of saying, don't look at the more natural holistic way of helping the body. 
Medicine believes disease is the enemy....Medicine fights disease. Natural health care 
works with it...."Medicine believes symptoms are evil. Natural health care believes 
symptoms are the body's efforts to rid itself of disease."
[413]Curtis Cost, author of Vaccines Are Dangerous: A Warning to the Black Community,
adds, "We know through...studies that the incidences of various diseases have been 
declining steadily prior to the advent of various vaccines. We see declines up to 90 
percent, and these declines result from improvements in sanitation and nutrition....
"My point is that parents do not need to be terrified into believing that the only way to 
protect themselves and their children from disease is through vaccines. We know that 
if parents breastfeed their babies, the risk of death and disease is dramatically reduced 
because the breast milk contains all the natural nutrients that the mother will naturally 
give to her child as she breastfeeds. We know that diet has a tremendous effect on 
disease. If you are not eating a proper diet your risk of getting various diseases is 
much greater. So we need to focus on taking control of our health...to focus on eating 
more organically grown fresh fruits and vegetables, on drinking pure water, and on 
exercising. These actions build up the immune system."
[414]
Finally, the point is that individuals need the freedom to choose. They should not be 
forced in one direction or another. Barbara Loe Fisher stresses this: "Our organization 
does not tell a parent what to do.
[415]
 I want to make that clear. We are an information 
clearinghouse and we believe in education. We believe that parents should take the 
responsibility for making their own decision. In this society, we ought to have the 
right to make the right decisions without being bullied and harassed and threatened 
into vaccinating if we do not believe that it is in the best interest of our child."
Alan Phillips reminds us that we are kept in the dark about our freedom to choose. 
"Most states currently allow for medical and religious exemptions. You are not told 
this when you go to a pediatrician or when you enter a university. You are simply told 
that you have to vaccinate. But that is not usually true. Probably 15 to 20 states have a 
philosophical or personal exemption option that you don't even have to tie to your 
religion.
"I don't advocate that people do or do not vaccinate. I say that there's a lot of 
information that people should investigate before they make a decision one way or the 
other. We're so steeped in what I would now call the myth of vaccination that it seems nonsensical and counterintuitive to even raise the question. In fact, the first time that I 
raised the question with a pediatrician I got yelled at. While I think that was 
unprofessional of the pediatrician, it does demonstrate the degree to which 
assumptions about vaccinations are held."
[416]
Dr. Black states, "As a parent, there might be times I choose to immunize my child. 
Maybe I would find scientific evidence to back its validity in a case where a disease is 
so fraught with risk that I dare not expose my child. Maybe then I would choose [to 
vaccinate]. But I would do so having thoroughly thought about it....What I believe we 
cannot tolerate as a free nation is to have government bureaucrats come in and saybased upon false statistics-if you don't immunize your child, you will suffer penalty of 
law. That, to me, is a gross injustice that simply has to be changed."
[417]
It stands to reason, then, that our approach might be better directed to bolstering the 
effects of natural immunity, by strengthening the body's own disease fighting 
capability, rather than trying to manipulate a carefully balanced system which may or 
may not tip to the detriment of the future individual.  The old adage, 'What doesn't kill 
you makes you stronger', describes the credo of the vaccine industry.  The problem is 
that we do not yet know a single silver bullet remedy for all childhood illnesses, that 
are known to cause no harm to the future adult.
To this argument, Trevor Gunn states, "for example, Vitamin A supplementation has 
been shown to reduce the mortality rate due to measles, in under 2 year olds, by seven 
times.  (From the British Medical Journal, 1987, p 294) "Many studies show 
increased eye problems and deaths in children with vitamin A deficiency."  In addition 
he cites the WHO's doctor Clements with regards to prevention of Cholera:  "the first 
line of defense should be providing safe clean water and proper waste disposal."
The culmination of a review of a larger study that we mentioned earlier, which 
compared over 15,000 data sets for Union Army Soldiers over two distinct time 
periods (1830-1845) and (1918-1927), showed that length of life was improved in the 
20
th
 century, and in addition age of onset of chronic illness was also delayed.  The 
reviewer Robert Fogel noted that there  were two distinct explanations: The first, combining several outcomes, mentions reduction in debilitating chronic illness by 
eliminating causes of childhood illness, and the second, "increases in birth weight and 
adult frame size, which are likely the result of better nutrition, have been important in 
reducing mortality among infants and adults." (from the How the Aging Process 
Changed During the 20
th
 Century, "Changes in the Process of Aging during the 20
th
Century:  Findings and Procedures of the Early Indicators project)  
Resources
Advisory Committee on Immunization Practices
Centers for Disease Control and Prevention
National Immunization Program
Division of Epidemiology and Surveillance
Mail Stop E61
1600 Clifton Road, NE
Atlanta, GA 30333Tel: 404-639-8096
Web site: www.cdc.gov/nip/ACIP/default.htm
    This is a pro-immunization site. To access the NIP's
"Locating Information on Vaccine Safety"guide, go to 
www.cdc.gov/nip/vacsafe/research/resourceguide.htm.
Association of American Physicians and Surgeons
1601 N. Tucson Blvd., Suite 9
Tucson, AZ 85716-3450
Tel: 800-635-1196
Web site: www.aapsonline.org
Citizens for Healthcare Freedom
P.O. Box 62282
Durham, NC 27715
Web site: www.unc.edu/~aphillip/www/chf/index.htm
    To read "Dispelling Vaccination Myths," by CHF director 
Alan Phillips, go to www.unc.edu/~aphillip/www/chf/myths/dvm1.htm
Concerned Parents for Vaccine Safety
8216 192nd St., Ct E
Spanaway, WA 98387Web site: home.sprynet.com/~gyrene
Gary Null's Web Site
Web site: www.garynull.com
Global Vaccine Awareness League
25422 Trabuco Road, Suite 105-230
Lake Forest, CA 92630-2797
Web site: www.gval.com
"Homeopathic Disease Prevention"
     This article by homeopathic practitioner Isaac Golden is available
at Homeopathy Online, a Journal of Homeopathic Medicine
Web site: www.lyghtforce.com/HomeopathyOnline/text/golden.htm
Immunization Action Coalition
1573 Selby Avenue
St. Paul, MN 55104
Tel: 651-647-9009
Web site: www.immunize.org
   This is a pro-immunization site. For information on "State mandates on vaccination and vaccine-preventable disease," go to www.immunize.org/laws
Institute for Vaccine Safety
Bloomberg School of Public Health
Johns Hopkins University 
Web site: www.vaccinesafety.edu
National Network for Immunization Information
66 Canal Center Plaza, Suite 600
Alexandria, VA 22314
Tel.: 877-341-6644
Fax: 703-299-0204
Web site: www.immunizationinfo.com
    This is a pro-immunization site.
National Vaccine Information Center 
421-E Church St.
Vienna, VA 22180
Tel.: 1-800-909-SHOT
Fax: 703-938-5768  
Web site: www.909shot.comParents Requesting Open Vaccine Education (PROVE)
P.O. Box 91566
Austin, TX 78709-1566
Web site: www.vaccineinfo.net
The Phyllis Schlafly Report
P.O. Box 618
Alton, IL 62002
Tel.: 618-462-5415
Web site: www.eagleforum.org/topics/vaccine/vaccine.html
    This site contains a number of articles on vaccine topics.
Thinktwice Global Vaccine Institute
P.O. Box 9638
Santa Fe, NM 87504
Web site: www.thinktwice.com
    Also includes the Thijnktwice/New Atlantean Press bookstore,
with a catalog of books on vaccination topics
Vaccination Information Service
     To order the video "Vaccination: The Hidden Truth."Web site: www.vaccination.inoz.com/default.html
Vaccination Liberation
P.O. Box 1444
Coeur d'Alene, Idaho 83816
Tel.: 208-255-2307
Web site: www.vaclib.org
Vaccine Adverse Event Reporting System (VAERS)
P.O. Box 1100
Rockville, MD 20849-1100
Tel: 800-822-7967
Fax: 877-721-0366
Web site: www.vaers.org
   A more usable version of the VAERS data is available on a database
developed by Steven Rubin. Go to www.nccn.net/~wwithin/vaers.htm
Vaccine Information and Awareness Web site
Tel.: 858-484-3197
Web site: www.access1.net/via
    To access a list of pro-information groups, go to www.access1.net/via/PROCHOICE/prochoic.htm
    To access state links, including information on state exemptions,
go to www.access1.net/via/STATES/toc-states.htm
Vaccine resources by state
Web site: http://proliberty.com/observer/vaclib/VACLIST.DOC
"Vaccines: The Risks, the Benefits, the Choices"
Doctor's Reference Manual (2001-02)
Presented by Sherri J. Tenpenny, D.O.
New Medical Awareness Seminars, LLC
14761 Pearl Road #263
Strongsville, OH 44136
Tel: 440-572-1136
Web site: www.osteomed.com
Vaccine Policy Institute
251 W. Ridgeway Drive
Dayton, OH 45459
Tel: 937-435-4750
Web site: www.vaccinepolicy.orgVaccineWebsite.com
Web site: www.whale.to/vaccines.html
"Alternative Approach to Disease" (video)
By Gary Null
"Building the Immune System Naturally" (video)
By Gary Null
The Consumer's Guide to Childhood Vaccines
By Barbara Loe Fisher
National Vaccine Information Center
Immunization Theory vs. Reality: Expos on Vaccinations
By Neil Z. Miller
The Atlantean Press, 1996
Immunization: The Reality Behind the Myth
By Walene James
Greenwood Publishing Group, 2nd Edition, 1995Reverse the Aging Process Naturally
By Gary Null and Martin Feldman, M.D.
Villard Books, a division of Random House, 1993
"Seven Steps to Perfect Health" (video)
By Gary Null
A Shot in the Dark
By Harris L. Coulter and Barbara Loe Fisher
Avery Publishing Group, 1991
"Supercharge Your Immune System" (video)
By Gary Null
"Total Health" series, Steps 1 - 7 (videos)
By Gary Null
Vaccination and Immunization: Dangers, Delusions & Alternatives
By Leon Chaitow
Beekman Publishing, 1996Vaccines Are Dangerous: A Warning to the Black Community
By Curtis Cost
A & B Distributors & Publishers Group, 1992
What Every Parent Should Know About Childhood Immunization
By Jamie Murphy
Earth Healing Products, 1993
Correspondence:
Gary Null, PhD
P.O. Box 918
Planetarium Station
New York, New York 10024 USA
646-505-4660/ Fax 212-472-5139
e-mail: precisemd@aol.comReferences
[1]
  
[1]
Clin Infect Dis. 2006 Mar 1;42 Suppl 3:S141-4 A response to strategy #2: streamlining the regulatory process.Glezen WP. 
[2]
Expert Rev Vaccines. 2003 Feb;2(1):15-9 Designing pediatric vaccine formularies and pricing pediatric combination vaccines using 
operations research models and algorithms. Jacobson SH, Sewell EC, 
[3]
 Clin Infect Dis. 2000 Jun;30 Suppl 3:S247-9 Moving new vaccines for tuberculosis through the regulatory process.Brennan MJ. 
  
[4]
MMWR Recomm Rep. 2006 Jul 28;55(RR-10):1-42 Prevention and Control of Influenza: recommendations of the 
Advisory Committee on Immunization Practices (ACIP).Advisory Committee on Immunization Practices; Smith NM,
  
[5]
 Vaccine. 2006 Apr 24;24(17):3530-7. Epub 2006 Feb 20 Stockpile levels for pediatric vaccines: how much is enough?Jacobson SH, 
Sewell EC, 
[6]
Health Aff (Millwood). 2005 May-Jun;24(3):635-42 Factors affecting U.S. manufacturers' 
decisions to produce vaccines.Coleman MS, Sangrujee N,
[7]
 MMWR Morb Mortal Wkly Rep. 2005 Apr 1;54(12):307-8 Influenza vaccine prebooking and distribution strategies for the 2005-06 
influenza season. Centers for Disease Control and Prevention (CDC). 
  
[8]
 MMWR Morb Mortal Wkly Rep. 2003 Jan 31;52(4):Q1-4. Recommended childhood and adolescent immunization schedule. United 
States, 2003. Centers for Disease Control and Prevention.Centers for Disease Control and Prevention (CDC). 
  [9]
 Public Health Rep. 2005 Sep-Oct;120(5):543-8 Enrollment of racial/ethnic minorities in NIAID-funded networks of HIV vaccine trials 
in the United States, 1988 to 2002.Djomand G, Katzman J, 
[10]
 Clin Infect Dis. 2005 Oct 15;41(8):1150-6. Epub 2005 Sep 2 Prospects for a group A streptococcal vaccine: rationale, feasibility, and 
obstacles--report of a National Institute of Allergy and Infectious Diseases workshop.Bisno AL, Rubin FA, 
[11]
: Curr Opin Obstet Gynecol. 2006 Feb;18 Suppl 1:s15-21. Harnessing the power of prevention: human papillomavirus 
vaccines.Mayeaux EJ Jr. 
  
[12]
Obstet Gynecol Surv. 2006 Jun;61(6 Suppl 1):S26-31. Vaccines for the prevention of human papillomavirus and associated 
gynecologic diseases: a review.Ault KA. 
  
[13]
Obstet Gynecol Surv. 2006 Jun;61(6 Suppl 1):S26-31. Vaccines for the prevention of human papillomavirus and associated 
gynecologic diseases: a review.Ault KA. 
  
[14]
http://www.mayoclinic.com/health/vaccines/HQ01629
[15]
http://www.nber.org/digest/mar02/w8556.html
[16]
http://www.nber.org/digest/mar02/w8556.html
[17]
http://www.nber.org/digest/mar02/w8556.html
[18]
http://www.nber.org/digest/mar02/w8556.html
[19]
http://www.nber.org/digest/mar02/w8556.html
[20]
http://www.nber.org/digest/mar02/w8556.html
[21]
http://www.whale.to/m/gunn.html, p.7. 
[22]
http://www.cdc.gov/nip/publications/fs/gen/WhatIfStop.htm
[23]
 http: /www.nber.org/aginghealth/fall03/w9941.html 
[24]
Circulation. 2003; 108:2957.) 2003 American Heart Association, Inc. Review: Current Perspective  Explaining How "High-Grade" 
Systemic Inflammation Accelerates Vascular Risk in Rheumatoid Arthritis  
Naveed Sattar, MD; David W. McCarey 
[25]
 Lavrovsky, Y, Chattergee, B, role of Redox regulated transcription factors in inflammation, aging, and age related diseases, 
Experimental gerontology 35 (2000) 521-532 [26] New England Journal of medicine  
Volume 352:1685-1695April 21, 2005
 number 16
Inflammation, 
Atherosclerosis, and Coronary Artery Disease  Gran K. Hansson, M.D., Ph.D. 
http://www.jacn.org/cgi/content/abstract/21/6/495
[27]
 Coronary artery disease and rheumatoid arthritis. Epidemiology and health-related services Current Opinion in 
Rheumatology. 14(2):115-120, March 2002. 
Goodson, Nicola MRCP http://www.co-rheumatology.com/pt/re/corheum/abstract.00002281-200203000-
00007.htm;jsessionid=FF5JM334D9JzKT6wQw2zS2HyRXQrVyF4G28v4P0vtmLGdLv2ln7S!1230047961!-949856144!8091!-
1
[28]
 Abuja, Peter M, Albertini, Riccardo, Methods for Monitoring oxidative stress, lipid peroxidation and oxidation resistance of 
lipoproteins, Clinica Chimica Acta 306 (2001) 1-17 
[29]
Biotechnology Journal Volume 1, Issue 4 , Pages 420 - 439Review: Essential fatty acids: biochemistry, physiology and pathology
  
[30]
 Pharmacological Reviews Vol. 52, Issue 4, 673-751, December 2000 
The Effects of Plant Flavonoids on Mammalian Cells:Implications for Inflammation, Heart Disease, and Cancer Elliott Middleton, Jr. , 
Chithan Kandaswami 
[31]
Experimental Biology and Medicine 231:1287-1299 (2006) 2006 Society for Experimental Biology and Medicine  
MINIREVIEW Flavonoids Attenuate Cardiovascular Disease, Inhibit Phosphodiesterase, 
and Modulate Lipid Homeostasis in Adipose Tissue and Liver Michael R. Peluso
1
http://www.ebmonline.org/cgi/content/abstract/231/8/1287
  
[32]
  2002 The American Society for Nutritional Sciences J. Nutr. 132:1825-1829, 2002 Biochemical and Molecular Actions of Nutrients 
Flavonoids of Cocoa Inhibit Recombinant Human 5-Lipoxygenase
1
Tankred Schewe, Hartmut Khn
*
 and Helmut Sies
23
http://jn.nutrition.org/cgi/content/abstract/132/7/1825
  
[33]
 PNAS | January 24, 2006 | vol. 103 | no. 4 | 1024-1029 (-)-Epicatechin mediates beneficial effects of flavanol-rich cocoa on vascular 
function in humans  Hagen Schroeter
 *  , 
, Christian Heiss
, http://www.pnas.org/cgi/content/abstract/103/4/1024
[34]
 Clinical and Vaccine Immunology, March 2006, p. 319-328, Vol. 13, No. 3 
doi:10.1128/CVI.13.3.319-328.2006Copyright  2006, American Society for Microbiology. All Rights Reserved. The Flavonoid 
Quercetin Inhibits Proinflammatory Cytokine (Tumor Necrosis Factor Alpha) Gene Expression in Normal Peripheral Blood Mononuclear 
Cells via Modulation of the NF-  System Madhavan P. Nair,
*
 Supriya Mahajan, http://cvi.asm.org/cgi/content/abstract/13/3/319
[35]
  2005 The American Society for Nutritional Sciences J. Nutr. 135:172-178, February 2005 Biochemical and Molecular Actions of 
Nutrients The Flavonoid Phloretin Suppresses Stimulated Expression of Endothelial Adhesion Molecules and Reduces Activation of 
Human Platelets Verena Stangl
*,1
, Mario Lorenz http://jn.nutrition.org/cgi/content/abstract/135/2/172
*
,[36]
 American Journal of Clinical Nutrition, Vol. 78, No. 3, 570S-578S, September 2003 
 2003 American Society for Clinical Nutrition Fruits and vegetables in the prevention of cellular oxidative damage
1,2,3,4,5
Ronald L Prior 
http://www.ajcn.org/cgi/content/abstract/78/3/570S
[37]
 (Arteriosclerosis, Thrombosis, and Vascular Biology. 2001;21:1084.) 2001 American Heart Association, Inc. Effect of Acute and 
Chronic Tea Consumption on Platelet Aggregation in Patients With Coronary Artery Disease Stephen J. Duffy; Joseph A. Vita 
[38]
 Journal of the American College of Nutrition, Vol. 21, No. 6, 495-505 (2002) 
Published by the American College of Nutrition Omega-3 Fatty Acids in Inflammation and Autoimmune Diseases Artemis P. 
Simopoulos, MD, FACN 
The Center for Genetics, Nutrition and Health, Washington, D.C
[39]
 American Journal of Clinical Nutrition, Vol. 76, No. 3, 560-568, September 2002 
 2002 American Society for Clinical Nutrition Flavonoid intake and risk of chronic diseases
1,2
Paul Knekt, Jorma 
Kumpulainenhttp://www.ajcn.org/cgi/content/abstract/76/3/560
[40]
Relationship Between Physical Activity and Inflammation Among Apparently Healthy Middle-aged and Older US Adults 
Jerome L. Abramson, PhD; Viola Vaccarino, MD, PhD  
Arch Intern Med. 2002;162:1286-1292. http://archinte.ama-assn.org/cgi/content/abstract/162/11/1286
[41]
 American Journal of Clinical Nutrition, Vol. 70, No. 3, 532S-538S, September 1999 
 1999 American Society for Clinical Nutrition Associations between diet and cancer, ischemic heart disease, and all-cause mortality in 
non-Hispanic white California Seventh-day Adventists
1,2,3
  
Gary E Fraser http://intl.ajcn.org/cgi/content/abstract/70/3/532S
  
[42]
 Medical careJanuary 1999, 37:1 >  Evidence Suggesting That a Chronic Disease Self-Management Program Can 
Improve Health Status While Reducing Hospitalization: A Randomized Trial. http://www.lwwmedicalcare.com/pt/re/medcare/abstract.00005650-199901000-
00003.htm;jsessionid=FF8ZLxQTfJhFFMrFJBys0Tc7Rb6GmSGLSLQ2sLlrbJ5rJ3YR1lpk!-210589086!-
949856145!8091!-1
[43]
Wei Young, Robert L. Hotovec, and Arthur G. Romero, "Tea and Atherosclerosis", Nature, December 9, 1967, Vol. 216, Num. 0, pp. 
1015-1016 http://www.healthsentinel.com/briefs.php?id=035&title=Coffee&event=briefs_print_list_item
[44]
 http: /www.nber.org/aginghealth/fall03/w9941.html p.2. 
[45]
 http: /www.nber.org/aginghealth/fall03/w9941.html p.2. 
[46]
 http: /www.nber.org/aginghealth/fall03/w9941.html p.2. 
[47]
http://www.vaclib.org/intro/present/index.htm#8, Vaccination, a parent's Dilemma 
[48]
 United States mortality rate from measles, scarlet fever, typhoid, whooping cough, and diphtheria, 
http://www.healthsentinel.com/graphs.php?id=14&event=graphs_print_list_item[49]
http://www.healthsentinel.com/graphs.php?id=14&event=graphs_print_list_item
[50]
 http: /www.nber.org/aginghealth/fall03/w9941.html p.2. 
[51]
Vaccine Safety Vaccines: A Safe Choice Vaccine Safety Information for Parents 
http://www.cdc.gov/nip/vacsafe/vacsafe-parents.htm
[52]
http://www.iahf.com/20020702.htmlUK babies given toxic vaccines, admits Glaxo
Antony Barnett and Tracy McVeigh Sunday June 30, 2002 The 
Observerhttp://www.observer.co.uk/uk_news/story/0,6903,746568,00.html
[53]
http://www.fda.gov/opacom/factsheets/justthefacts/19vaccine.html Vaccines Provide Effective Protection and FDA Makes Sure They 
are Safe 
[54]
http://www.eagleforum.org/educate/1998/nov98/vaccinations.html
Compulsory Vaccinations Put American Children at Risk
[55]
http://www.k12.dc.us/dcps/policies/policies_intro.html#immunization Immunization Requirements
[56]
http://www.cispimmunize.org/IZSchedule_2006.pdf-  -immunization chart 
  
[57]
http://www.npr.org/templates/story/story.php?storyId=4585992&sourceCode=RSS
Salk Polio Vaccine Conquered Terrifying Disease Source: Global Polio Eradication Initiative U.S. Centers for Disease Control and 
Prevention; the University of Michigan; PBS Online
[58]
 Polio Vaccine: It Tamed a Scourge, Transformed Medicine Related Health News By Amanda GardnerHealthDay Reporter 
TUESDAY, April 12 (HealthDay News) Nancy Green, M.D., medical director, March of Dimes, White Plains, N.Y.; David Rose, archivist, March 
of Dimes, White Plains, N.Y. 
[59]
http://www.unicef.org/media/media_18979.html Information note 2004 - Now More than Ever: End Polio 
Forever
[60]
http://www.fda.gov/Cber/vaers/articles.htmVaccine Adverse Event Report System (VAERS):
Documents
FEDERAL REGISTER: Vaccine Adverse Event Reporting; Revised Form VAERS-2; 
Withdrawal of Proposed Revised Form - 4/21/2006 - (PDF), (Text)
         Federal Register Notice; Vaccine Adverse Event Reporting System; Revised Form VAERS-2; Availability - 
11/20/2001 - (PDF), (Text)  
         Draft Form (for comment) - (PDF), Instructions - (PDF)  Guidance for Industry: How to Complete the Vaccine Adverse Event Reporting System Form 
(VAERS-1) - 9/8/1998 (PDF), (Text)
Dear Colleague Letter: Use of Haemophilus influenzae Vaccines in Combination with DTaP 
in Infants - 8/12/1998 
VAERS Bibliography: CDC/FDA Publications
Consumer Articles  
1.      How the FDA works to Ensure Vaccine Safety FDA Consumer December 1995  
2. Adults Need Tetanus Shots, Too FDA Consumer July-August 1996  
3. First Vaccine for Chickenpox FDA Consumer September 1995  
4. Vaccine Safety Crucial but Impossible to Guarantee. Infectious Diseases in Children, 1996;9(1):33-35.  
5.      Physicians play a pivotal role in vaccine safety. AAP News, Feb., 1996.  
Professional Articles  
1.      Ball LK, Ball R, Pratt RD. Assessment of thimerosal use in childhood vaccines. Pediatrics 2001;107:1147-
1154.  
2.      Ball R, Ball LK, Wise R, Braun MM, Beeler JA, Salive M. Stevens Johnson syndrome and toxic epidermal 
necrolysis after vaccination: Reports to the Vaccine Adverse Event Reporting System. Pediatric Infectious 
Disease Journal 2001;20:219-223.  
3.      Ball R, Braun MM, Mootrey GT. Safety data on meningococcal polysaccharide vaccine from the Vaccine 
Adverse Event Reporting System. Clinical Infectious Diseases 2001;32:1273-1280.  
4.      Beeler J, Varricchio F, Wise RP. Thrombocytopenia after immunization with measles vaccines: Review of the 
Vaccine Adverse Events Reporting System (1990 to 1994). The Pediatric Infectious Disease Journal. 
1996;15:1,88-90.  
5.      Braun MM, Ellenberg SS. Descriptive epidemiology of adverse events following immunization: reports to the 
Vaccine Adverse Events Reporting System (VAERS), 1991-1994. Journal of Pediatrics 1997; 131:529-35.  
6.      Braun MM, Mootrey GT, Salive ME, Chen RT, Ellenberg SS, and the VAERS Working Group. Infant 
immunization with acellular pertussis vaccines in the US: Assessment of the first two years' data from the 
Vaccine Adverse Event Reporting System (VAERS). Pediatrics electronic pages 2000;106:e51 and Pediatrics 
2000;106:821.  
7.      Braun MM, Patriarca PA, Ellenberg SS. Syncope after immunization. Archives of Pediatrics and Adolescent 
Medicine. 151:255-9; 1997.  8.      Braun MM, Terracciano G, Salive ME, Blumberg DA, Vermeer-de Bondt PE, Heijbel H, Evans G, Patriarca 
PA, Ellenberg SS. Report of a US Public Health Service Workshop on Hypotonic-Hyporesponsive Episode 
(HHE) Following Pertussis Immunization. Pediatrics electronic pages 1998;102:e52 and Pediatrics 
1998;102:1201-2.  
9.      Centers for Disease Control and Prevention. Vaccine Adverse Event Reporting System-United States. MMWR 
Morbidity and Mortality Weekly Report, 1990; 39(RR-41):730-33.  
10.  Chen RT, Glasser JW, Rhodes PH, Wise RP, et. al. Vaccine Safety Datalink Project: A new tool for improving 
vaccine safety monitoring in the United States. Pediatrics. 99(6):765-73;1997.  
11.  Chen RT, Rastogi SC, Mullen JR et. al. The Vaccine Adverse Event Reporting System (VAERS). Vaccine. 
1994;12:542-50.  
12.  Chen RT, Phillips L, Hadler S. Bottom Line: Vaccination benefits far outweigh risks [letter]. The Nations 
Health, Dec. 1995;2.  
13.  Clements, CJ, Ball, LK, Ball, R. Ball, Pratt, RD. Thiomersal in vaccines (letter). Lancet, 2000; 355:1279-1280.  
14.  Commentary. CDC Officials help physicians answer DTP-safety questions. American Academy of Pediatrics 
News, 1995; 11(3):9-11.  
15.  DuVernoy TS, Braun MM. Hypotonic Hyporesponsive Episodes Reported to the Vaccine Adverse Event 
Reporting System (VAERS), 1996-1998. Pediatrics electronic pages 2000;106:e52 and Pediatrics 2000;106:821-
2.  
16.  Ellenberg SS, Chen RT, The complicated task of monitoring vaccine safety. Public Health Reports, 112:10-20, 
1997.  
17.  Howson, et al. Adverse Effects of Pertussis and Rubella Vaccines. Washington, DC: National Academy Press, 
1991.  
18.  Niu MT, Davis, DM, and Ellenberg SS. Recombinant hepatitis B vaccination of neonates and infants: 
Emerging safety data from the Vaccine Adverse Event Reporting System. Pediatric Infectious Disease Journal, 
1996;15:771-76.  
19.  Niu MT, Rhodes P, Salive ME, Lively T, Davis DM, et. al. Comparative safety of two recombinant hepatitis B 
vaccines in children: data from the Vaccine Adverse Event Reporting System (VAERS) and Vaccine Safety 
Datalink (VSD). Journal of Clinical Epidemiology, 1998; Vol 51, 6:503-510.  
20.  Niu MT, Salive ME, Krueger CL, Ellenberg SS. Two year review of hepatitis A vaccine safety: Data from the 
Vaccine Adverse Event Reporting System (VAERS). Clinical Infectious Disease 1998;26:1475-6.  
21.  Niu MT, Salive ME, Ellenberg SS. Post-marketing surveillance for adverse events after vaccination: The 
national Vaccine Adverse Event Reporting System (VAERS), MEDWATCH CME credit article (FDA/CBER 
publication), November, 1998.  
22.  Niu MT, Salive ME, Ellenberg SS. Reporting adverse events after vaccination: The national Vaccine Adverse 
Event Reporting System (VAERS) Federal Practitioner 1998; 15; 13-21,37.  23.  Niu MT, Salive ME, Ellenberg SS. Neonatal deaths after hepatitis B vaccine, VAERS, 1991-1998. Arch Pediatr 
Adoles Med 1999; 153:1279-82.  
24.  Rosenthal S, Chen RT. The reporting sensitivities of two passive surveillance systems for Vaccine Adverse 
Events. American Journal of Public Health, 1995; 85(12):1706-09.  
25.  Singleton JA, Loyd, JL, Mootrey, GT, Salive, ME, Chen, RT. An overview of the Vaccine Adverse Event 
Reporting System (VAERS) as a surveillance system. Vaccine 1999;17(22):2908-17.  
26.  Stratton, et al. Adverse Events Associated with Childhood Vaccines, Evidence Bearing on Causality. 
Washington, DC: National Academy Press, 1993.  
27.  Varricchio, F. The vaccine adverse event reporting system. Clinical Toxicology, 36(7), 765-68 (1998).  
28.  Wise RP, Kiminyo KP, Salive ME. Hair loss following routine immunizations. Journal of the American 
Medical Association. 1997; 278:1176-8.  
29.  Wise RP, Salive ME, Braun MM, Mootrey GT, Seward JF, Rider LG, Krause PR, Postlicensure safety 
surveillance for varicella vaccine, Journal of the American Medical Association, September 13, 2000, 
284(10):1271-9.  
         Supplementary references  
Zanardi LR, Haber P, Mootrey GT, Niu, MT, Wharton M. Intussusception among recipients of 
rotavirus vaccine--reports to the Vaccine Adverse Event Reporting System, 2001; Pediatrics , in press.  
[61]
 June Russell's Health FactsVaccinations http://www.jrussellshealth.com/immune.html{"Fitness On Line" - Nov. 1999 Natural 
Health magazine}{"Vaccination: Prevention or Poison?" Delicious magazine, Sept. 1994, by Kathleen Finn} {"Vaccinations - Deception 
and Tragedy" - Michael Dye} Health Freedom News - May 1984. "How Do The Vaccines Work?" Richard Moskowitz, 
MD}{"Supporting Children's Health" - Philip Incao, MD, Alternative Medicine Digest, Aug./Sept. 1997} According to an article in The 
Lancet (1985), "Measles Virus Infection Without Rash in Childhood is Related to Disease in Adult Life," Leon Chaitow in his book, 
"Vaccinations and Vaccinations: Dangers Delusions and Alternatives," 
  
[62]
 Vaccination Debate: Do Vaccines Cause Cot Deaths? Harris L. Coulter, 
PhD, http://www.pnc.com.au/~cafmr/coulter/vacc-deb.html
  
[63]
 Virchows Arch. 2006 Jan;448(1):100-4. Epub 2005 Oct 18. Sudden infant death syndrome (SIDS) shortly after hexavalent vaccination: 
another pathology in suspected SIDS? Ottaviani G, Lavezzi AM, 
[64]
 National Academy of sciences Press Relaease Date: March 12, 2003  http://www.cdc.gov/nip/publications/#Diseaseshadalready 'SIDS 
Not Linked to Number and Variety of Childhood Vaccines', says IOM
[65]
http://www.fda.gov/fdac/features/2001/401_vacc.htmlU.S. Food and Drug AdministrationFDA Consumer magazineJuly-August 2001 
Understanding Vaccine Safety: Immunization Remains Our Best Defense Against Deadly Disease 'Alleged Associations' [66]
http://www.fda.gov/fdac/features/095_vacc.html Developing New Pertussis Vaccines
[67]
 Am J Prev Med. 2002 Apr;22(3):170-6. Pediatric deaths reported after vaccination: the utility of information obtained from 
parents.Silvers LE, Varricchio FE, 
[68]
 Pharmacoepidemiol Drug Saf. 2001 Jun-Jul;10(4):279-85. The epidemiology of fatalities reported to the vaccine adverse event 
reporting system 1990-1997.Silvers LE, Ellenberg SS, 
[69]
J Paediatr Child Health. 2003 Sep-Oct;39(7):487-91 Immunization myths and realities: responding to arguments against 
immunization.MacIntyre CR, Leask J. Children's Hospital at Westmead, Westmead and University of Sydney, Sydney, New South 
Wales, Australia. RainaM@chw.edu.au
  
[70]
 Vaccine. 2006 Aug 4; Sudden infant death syndrome: No increased risk after immunisation. Vennemann MM, Butterfass-Bahloul T, 
[71]
http://www.answers.com/topic/cigarette cigarette 
[72]
http://www.upenn.edu/pnc/ptverkuil.html "A Leadership Case Study of Tobacco and its Regulation" Paul Verkuil Benjamin N. 
Cardozo School of Law 
[73]
http://www.brownandcrouppen.com/news.html Lawsuit Charges HRT Caused Breast Cancer and Debilitating Stroke 
[74]
http://www.medicalnewstoday.com/medicalnews.php?newsid=50004Hormone Replacement Therapy Study 
Good News For Some POSTED: 5:43 p.m. PDT August 26, 2003
[75]
 http://www.chron.com/disp/story.mpl/ap/fn/4178876.html  Sept. 11, 2006, 5:48PM
Lawyers Say Wyeth Drugs Promoted Cancer By ANDREW DeMILLO Associated Press Writer  2006 The
Associated Press
[76]
 Hormone replacement therapy (HRT) http://www.nlm.nih.gov/medlineplus/ency/article/007111.htm
[77]
Hormone replacement therapy (HRT) http://www.nlm.nih.gov/medlineplus/ency/article/007111.htm
  
[78]
http://www.brownandcrouppen.com/news.htmlNIH Sends 11,000 Letters to Estrogen-Alone Study ParticipantsThe National Institutes 
of Health (NIH) has advised participants in the Women's Health Initiative (WHI) to stop taking their estrogen-alone study pills due to 
stroke risk and other findings in otherwise healthy women.
[79]
http://www.ahrp.org/infomail/04/10/12.php Pre 2006 Archives of the Alliance for Human Research Protection How Did the Vioxx 
Debacle Happen? USA Today / Lancet Tue, 12 Oct 2004 
[80]
http://www.flexicose.com/flexicose/COX-2-Death.html
Cox-II Inhibitors - Why They "Work" and Also Why They Can Potentially be Fatal[81]
First of four parts http://www.dailypress.com/news/dp-anthday1dec02,0,7450119.story?coll=dp-widget-news
An Incomplete Picture Despite promises that hospitalizations after anthrax vaccinations would be 
reported, the Pentagon withheld data on more than 20,000 cases.  BY BOB EVANS December 4, 
2005
[82]
http://www.vaccinationnews.com/Adverse_Reactions/VAERS/credible_estimates.htmJames Froeschle, Connaught Laboratories, 
Swiftwater, Pennsylvania 
[83]
http://medicine.plosjournals.org/perlserv/?request=advancedsearch&row_start=1&limit=10&order=score&search_fulltext=1&issn=1549-1676&jrn_issn=1549-
1676&anywhere_type=any&anywhere=Frequency+of+Adverse+Events+after+Vaccination+with+Different+Vacci
nia+&x=15&y=16 Frequency of Adverse Events after Vaccination with Different Vaccinia Strains Mirjam 
Kretzschmar
1,2*
, Jacco Wallinga
1
[84]
http://www.vaccinationnews.com/Adverse_Reactions/VAERS/credible_estimates.htmJamesDavid Kessler 
statement in JAMA - June 2, 1993,vol.269, No.21, p.2785
[85]
 Murphy, Jamie. What Every Parent Should Know About Childhood Immunization, Earth Healing Products, 
Boston, 1993. http://www.amazon.com/Every-Parent-Should-Childhood-Immunization/dp/0963037307/sr=1-
14/qid=1158257640/ref=sr_1_14/102-3250943-7888120?ie=UTF8&s=books
[86]
http://darwin.nap.edu/books/0309057914/html/29.html Research to Identify Risks for Adverse Events 
Following Vaccination: Biological Mechanisms and Possible Means of Prevention Cynthia J. Howe, Richard B. 
Johnston, and E. Russell Alexander, Editor
National Academies Press
[87]
http://www.dailycamera.com/bdc/broomfield_home_life/article/0,1713,BDC_11938_4928345,00.html Shots all around As school gets 
under way, so should children's immunization By Terri Chance, Enterprise Staff Writer August 19, 2006
[88]
http://wmc.who.int/pdf/Vaccine_Adverse_Events_in_the_New_Mill.pdf#search=%22age%20vaccination%20adverse%20events%22
Vaccine adverse events in the new millennium: is there reason for ...concern?  BJ Ward p.208 
[89]
http://www.immregistries.org/news/advocacy.phtml
ADVOCACY
AIRA is proud to be a member of the 317 Coalition (http://www.317coalition.org). Formed in April 2006, the 
sole focus of the coalition is advocating for increased 317 funds. 
Update on FY 2007 Labor HHS Appropriations Bill CDC Immunization Funding (Section 317) [90]
http://www.hhs.gov/news/speech/2003/030320.html TOMMY G. THOMPSON, SECRETARY 
OF HEALTH AND HUMAN  SERVICES Before the House Appropriations Subcommittee on 
Labor, HHS, Education March 20, 2003 p.2,
[91]
 Braun MM, et al. Descriptive epidemiology of adverse events after immunization: reports to the 
Vaccine Adverse Event Reporting System (VAERS), 1991-1994. J Pediatr 1997 Oct; 131(4):529-
35.
[92]
http://www.vaccinationnews.com/Adverse_Reactions/VAERS/credible_estimates.htmConnaught 
testimony to the Institute of Medicine
[93]
 The anthrax vaccine: New questions, weak data  
Posted on Fri, Dec. 09, 2005 http://www.charlotte.com/mld/charlotte/news/nation/13368280.htm  
The anthrax vaccine: New questions, weak data Over 20,000 troops hospitalized from anthrax 
vaccine Sun, Dec 11 2005 10:02 pm
[94]
http://whale.to/vaccines/studies.html Vaccine long term studies
[95]
http://www.vaccinesafety.edu/mmrandibd.htm The following Research Letter appeared in The 
Lancet Vol 351 - May 2, 1998. pg 1327-8. No evidence for measles, mumps, and rubella vaccineassociated inflammatory bowel disease or autism in a 14-year prospective study
[96]
http://www.cfah.org/hbns/getDocument.cfm?documentID=1154  Release Date:October 18, 
2005, 7:01 PM US Eastern time Newest Study Finds No Link Between MMR Vaccine and 
AutismBy Laura Kennedy, Contributing Writer  
Health Behavior News Service
[97]
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1623536
1&dopt=AbstractCochrane Database Syst Rev. 2005 Oct 19;(4):CD004407.Vaccines for 
measles, mumps and rubella in children.Demicheli V, Jefferson T, Rivetti A, Price D.
[98]
http://www.vaccines.bizland.com/lkj.htmFact #1: Approximately 1/3 of Doctors Refuse Vaccinations, yet . . 
[99]
 JAMA. 1981 Feb 20;245(7):711-3. Rubella vaccine and susceptible hospital employees. Poor physician participation. Orenstein WA, 
Heseltine PN, 
[100]
Mendelsohn, Dr. Robert, "The Drive to Immunize Adults," Herald of Holistic Health Newsletter, 
Sept.-Oct. 1985. Yih WK, Lieu TA, [101]
 Orenstein WA, Heseltine PN, LeGagnoux SJ, Portnoy B. Rubella vaccine and susceptible hospital employees. 
Poor physician participation. JAMA 1981 Feb 20; 245(7):711-3.
[102]
http://occmed.oxfordjournals.org/cgi/reprint/54/4/231.pdf#search=%22Attitudes%20of%20general%20practitioners%20towards%20th
eir%20vaccination%20against%20hepatitis%20B.%22:  Management of hepatitis B immunizations and blood exposure incidents in 
primary care  Occupational medicine 2004; 54:  231-237  DOI: 10.1093/occmed/kgh 037 
  
[103]
 Kinnersley P. Attitudes of general practitioners towards their vaccination against hepatitis B. BMJ 1990 Jan 27; 
300(6719):238.
[104]
http://occmed.oxfordjournals.org/cgi/reprint/54/4/231.pdf#search=%22Attitudes%20of%20gen
eral%20practitioners%20towards%20their%20vaccination%20against%20hepatitis%20B.%22:  
Management of hepatitis B immunizations and blood exposure incidents in primary care  
Occupational medicine 2004; 54:  231-237  DOI: 10.1093/occmed/kgh 037
  
[105]
 Gary Null Interview with Jamie Murphy, December 18, 1997.
[106]
 James, Walene. Immunization: The Reality Behind the Myth, Bergin & Gervey, Massachusetts, 1988. 
[107]
 Gary Null Interview with Walene James, April 6, 1995.
[108]
 Gary Null Interview with Jamie Murphy, December 18, 1997.
[109]
 Phillips, Alan. Vaccination: dispelling the myths. Nexus, October-November 1997.
[110]
 J Infect Dis. 1994 Jan;169(1):77-82.Sustained transmission of mumps in a highly vaccinated population: assessment of primary 
vaccine failure and waning vaccine-induced immunity.Briss PA, Fehrs LJ,  
[111]
 Ibid.
[112]
 Clin Immunol Immunopathol. 1996 May;79(2):163-70 Changes within T cell receptor V beta subsets in infants following measles 
vaccination. Auwaerter PG, Hussey GD, 
[113]
 Auwaerter PG, Hussey GD, Goddard EA, Hughes J, et al. Changes within T cell receptor V beta subsets in 
infants following measles vaccination. Clin Immunol Immunopathol 1996 May; 79(2):163-70.
110
 J Infect Dis. 1994 Jan;169(1):77-82. 
Sustained transmission of mumps in a highly vaccinated population: assessment of primary vaccine 
failure and waning vaccine-induced immunity.Briss PA, Fehrs LJ, Parker RA114
Clin Immunol Immunopathol. 1996 May;79(2):163-70 Changes within T cell receptor V beta subsets in infants 
following measles vaccination.Auwaerter PG, Hussey GD, 
113
Auwaerter PG, Hussey GD, Goddard EA, Hughes J, et al. Changes within T cell receptor V beta subsets in 
infants following measles vaccination. Clin Immunol Immunopathol 1996 May; 79(2):163-70.
  
[114]
 Morbidity and Mortality Weekly Report 
Centers for Disease Control and Prevention
1600 Clifton Rd, MailStop K-95, Atlanta, GA 30333, U.S.A
  Department of Health
and Human ServicesThis page last reviewed 5/2/01 Recommendations and Reports 
 July 12, 1996 / 45(RR11);1-25 Prevention of Varicella: Recommendations of the Advisory Committee on 
Immunization Practices (ACIP) 
Summary 
[115]
 Am J Perinatol. 2003 Aug;20(6):321-32. A population-based study of the effects of birth weight on early developmental delay or
disability in children.Thompson JR, Carter RL,  
  
[116]
 Natl Vital Stat Rep. 2003 Jun 25;51(11):1-20.  Links  
Births: preliminary data for 2002.Hamilton BE, Martin JA, Sutton PD; U.S. Department of Health and Human Services Centers for 
Disease Control and Prevention. 
[117]
 Scholl, T., et al. Dietary and serum folate: their influence on the outcome of pregnancy. American Journal of Clinical Nutrition, 
volume 63, April 1996, pages 520-525.  
  
[118]
http://www.marchofdimes.com/professionals/681_1153.asp
114
 Morbidity and Mortality Weekly Report 
Centers for Disease Control and Prevention
1600 Clifton Rd, MailStop K-95, Atlanta, GA 30333, U.S.A  Department of Health
and Human ServicesThis page last reviewed 5/2/01 Recommendations and Reports 
 July 12, 1996 / 45(RR11);1-25 Prevention of Varicella: Recommendations of the Advisory Committee on 
Immunization Practices (ACIP) 
Summary 
[120]
 Morbidity and Mortality Weekly Report 
Centers for Disease Control and Prevention
1600 Clifton Rd, MailStop K-95, Atlanta, GA 30333, U.S.A
  Department of Health
and Human ServicesThis page last reviewed 5/2/01 Recommendations and Reports 
 July 12, 1996 / 45(RR11);1-25 Prevention of Varicella: Recommendations of the Advisory Committee on 
Immunization Practices (ACIP) 
Summary 
[121]
 Morbidity and Mortality Weekly Report 
Centers for Disease Control and Prevention
1600 Clifton Rd, MailStop K-95, Atlanta, GA 30333, U.S.A
  Department of Health
and Human ServicesThis page last reviewed 5/2/01 Recommendations and Reports 
 July 12, 1996 / 45(RR11);1-25 Prevention of Varicella: Recommendations of the Advisory Committee on 
Immunization Practices (ACIP) 
Summary 
[122]
 Morbidity and Mortality Weekly Report 
Centers for Disease Control and Prevention
1600 Clifton Rd, MailStop K-95, Atlanta, GA 30333, U.S.A
  Department of Healthand Human ServicesThis page last reviewed 5/2/01 Recommendations and Reports 
 July 12, 1996 / 45(RR11);1-25 Prevention of Varicella: Recommendations of the Advisory Committee on 
Immunization Practices (ACIP) 
Summary 
[123]
 Gary Null interview with Dr. Dean Black, April 7, 1995.
[124]
 Cournoyer, op. cit., p. 150-1.
[125]
 Miller, Neil Z. Vaccines: Are They Really Safe and Effective? A Parent's Guide to Childhood Shots, New 
Atlantean Press, Santa Fe, NM, 1992, p. 46.
[126]
 Lovett, Lisa, et al. Immunity, Why Not Keep It? Technical Publications, Victoria, Australia.
[127]
 Yves De Latte. Vaccinations: The Untold Truth, AUM Publications, San Antonio, TX, 1990, p. 65.
[128]
 Miller NZ, op. cit.
[129]
 Hearings Before the Committee on Interstate and Foreign Commerce, House of Representatives, 87
th
 Congress, 
Second Session on H.R. 10541, May 1962, p. 94.
[130]
 Coulter, Harris L and Fisher, Barbara Loe. A Shot in the Dark, Avery Publishing Group, Garden City Park, NY, 1991. 
[131]
 Coulter, Harris L. Vaccination, Social Violence, and Criminality, North Atlantic Books, Berkeley, CA, 1990. 
[132]
 Gary Null Interview with Dr. Harris Coulter, April 6, 1995.
[133]
Australian Nurses Journal, June 1981.
[134]
 Gary Null Interview with Alan Phillips, December 17, 1997.
[135]
 Gary Null Interview with Steven Lanka, 
[136]
 Phillips, op. cit.
[137]
 Gary Null Interview with Walene James, April 6, 1995.
[138]
 Merck & Co., Inc. Prescribing information for Recombivax HB Hepatitis B Vaccine (Recombinant). Issued 
August 2002.
[139]
 SmithKline Beecham Pharmaceuticals. Prescribing information for Engerix-B Hepatitis B Vaccine 
(Recombinant). Date of issuance November 2001.
[140]
 Merck & Co., op. cit.[141]
 Aventis Pasteur Inc. Prescribing information for Diphtheria and Tetanus Toxoids and Acellular Pertussis 
Vaccine Absorbed, Tripedia. Product information as of September 2000.
[142]
 SmithKline Beecham Pharmaceuticals. Prescribing information for Infanrix Diphtheria and Tetanus Toxoids 
and Acellular Pertussis Vaccine Absorbed. Date of issuance December 2001.
[143]
 Aventis Pasteur Inc. Prescribing information for Poliovirus Vaccine Inactivated, IPOL. Product information as 
of December 1999.
[144]
 Merck & Co., Inc. Prescribing information for M-M-R II (Measles, Mumps, and Rubella Virus Vaccine Live). 
Issued August 2001.
[145]
 Merck & Co., Inc. Prescribing information for Varivax [Varicella Virus Vaccine Live (Oka/Merck)]. Issued 
November 2000.
[146]
 Phillips, op. cit.
[147]
 Murphy, op. cit., p. 5.
[148]
 Thimerosal in Vaccines: A Joint Statement of the American Academy of Pediatrics and the Public Health Service. MMWR
07/09/1999; 48(26):563. 
[149]
 Thimerosal and vaccines: an Institute of Medicine (IOM) report. Centers for Disease Control and Prevention, 
National Immunization Program, Atlanta, GA. From http://www.cdc.gov/nip/vacsafe/concerns/thimerosal/iomthim10-1-01.htm Last modified October 24, 2001.
[150]
 Thimerosal in vaccines: frequently asked questions. Food and Drug Administration. From 
www.fda.gov/cber/vaccine/thimfaq.htm. Last updated October 5, 2001.
[151]
 Ibid.
[152]
 Sakamoto M, et al.Widespread neuronal degeneration in rats following oral administration of methylmercury during the postnatal
developing phase: a model of fetal-type minamata disease. Brain Res 1998 Feb 16; 784(1-2):351-4. 
[153]
 Echeverria D, et al. Neurobehavioral effects from exposure to dental amalgam Hg(o): new distinctions between recent exposure and 
Hg body burden. FASEB J 1998 Aug; 12(11):971-80. 
[154]
 Myers GJ, et al. A review of methylmercury and child development. Neurotoxicology 1998 Apr; 19(2):313-28. 
[155]
 Myers GJ, et al. Prenatal methylmercury exposure and children: neurologic, developmental, and behavioral research. Environ Health 
Perspect 1998 Jun; 106 Suppl 3:841-7. 
[156]
 Thimerosal in vaccines: frequently asked questions, op cit.
[157]
 Immunization update 2002: influenza vaccine. Centers for Disease Control and Prevention, Atlanta, GA. 
Satellite broadcast, August 15, 2002. From http://www.cdc.gov/flu/professionals/bulletin/2002-
03/bulletin4_091302.htm[158]
 FDA approves preservative-free influenza vaccine for pediatric use. Press release. Aventis Pasteur. September 
12, 2002.
[159]
http://www.cdc.gov/nip/vaccine/vacc-timeline.htm
[160]
http://www.cdc.gov/nip/vaccine/vacc-timeline.htm
[161]
http://www.pdhealth.mil/deployments/gulfwar/enviro_anthrax_vac.asp
[162]
 Phillips, op. cit.
[163]
 Measles vaccine failures: lack of sustained measles specific immunoglobulin G responses in revaccinated 
adolescents and young adults. Pediatr Infect Dis J 1994 Jan; 13(1):34-8. 
[164]
 Measles outbreak in 31 schools: risk factors for vaccine failure and evaluation of a selective revaccination 
strategy. Can Med Assoc J 1994 Apr 1; 150(7):1093-8. 
[165]
 Haemophilus b disease after vaccination with haemophilus b polysaccharide or conjugate vaccine. Am J Dis 
Child 1991 Dec; 145(12):1379-82.
[166]
 Sustained transmission of mumps in a highly vaccinated population: assessment of primary vaccine failure and 
waning vaccine-induced immunity. J Infect Dis 1994 Jan 1; 169(1):77-82.
[167]
 Secondary measles vaccine failure in healthcare workers exposed to infected patients. Infect Control Hosp 
Epidemiol 1993 Feb; 14(2):81-6.
[168]
 Failure to reach the goal of measles elimination. apparent paradox of measles infections in immunized persons. 
Arch Intern Med 1994 Aug 22; 154(16):1815-20. 
[169]
 Auwaerter, op. cit. 
[170]
 Outbreak of paralytic poliomyelitis in oman; evidence for widespread transmission among fully vaccinated 
children. Lancet 1991 Sep 21; 338:715-20.
47
http://www.vaclib.org/intro/present/index.htm#8, Vaccination, a parent's Dilemma 
48
 United States mortality rate from measles, scarlet fever, typhoid, whooping cough, and diphtheria, 
http://www.healthsentinel.com/graphs.php?id=14&event=graphs_print_list_item
49
http://www.healthsentinel.com/graphs.php?id=14&event=graphs_print_list_item
50
http://www.nber.org/aginghealth/fall03/w9941.html
[171]
 Sato H, et al. Experience with diphtheria toxoid-tetanus toxoid-acellular pertussis vaccine in Japan. Clin Infect Dis 1999 Jun; 28 
Suppl 2:S124-30. 
[172]
 Williams, AL. News and perspectives: new vaccines for childhood immunization. Drug Benefit Trends 1997; 9(3):10-11,15-22. [173]
 Rosenthal S, Chen R, Hadler S. The safety of acellular pertussis vaccine vs whole-cell pertussis vaccine. A postmarketing assessment. 
Arch Pediatr Adolesc Med 1996 May; 150(5):457-60. 
[174]
 Halperin SA, et al. Persistence of pertussis in an immunized population: results of the Nova Scotia Enhanced Pertussis Surveillance 
Program. J Pediatr 1989 Nov; 115(5 Pt 1):686-93. 
[175]
 de Melker, HE., et al. Pertussis in the Netherlands: an outbreak despite high levels of immunization with whole-cell vaccine. 
Emerging Infectious Diseases 1997; 3(2):175-8. Centers for Disease Control. 
[176]
 Hutchins SS, et al. Current epidemiology of pertussis in the United States. Tokai J Exp Clin Med 1988; 13 Suppl:103-9. 
[177]
 Ranganathan S, et al. Pertussis is increasing in unimmunized infants: is a change in policy needed? Arch Dis Child 1999 Mar; 
80(3):297-9. 
[178]
 Williams GD, et al. Infant pertussis deaths in New South Wales 1996-1997. Med J Aust 1998 Mar 16; 168(6):281-3. 
[179]
 Cournoyer, op. cit., p. 42.
[180]
 Whooping Cough, the DPT Vaccine and Reducing Vaccine Reactions. National Vaccine Information Center, 
Vienna, VA.
[181]
 Miller DL, et al. Pertussis immunisation and serious acute neurological illness in children. Br Med J 1981 May 
16; 282(6276):1595-9.
[182]
 Gale JL, et al.  Risk of serious acute neurological illness after immunization with diphtheria-tetanus-pertussis 
vaccine. A population-based case-control study. JAMA 1994 Jan 5; 271(1):37-41.
[183]
 Menkes JH, et al. Workshop on neurologic complications of pertussis and pertussis vaccination. 
Neuropediatrics 1990 Nov; 21(4):171-6.
[184]
 Murphy JV, et al. Recurrent seizures after diphtheria, tetanus, and pertussis vaccine immunization. Onset less 
than 24 hours after vaccination. Am J Dis Child 1984 Oct; 138(10):908-11.
[185]
 Stetler HC, et al. History of convulsions and use of pertussis vaccine. J Pediatr 1985 Aug; 107(2):175-9.
[186]
 Hirtz DG, et al. Seizures following childhood immunizations. J Pediatr 1983 Jan; 102(1):14-8.
[187]
 Odent MR, et al. Pertussis vaccination and asthma: is there a link? JAMA 1994 Aug 24-31; 272(8):592-3.
[188]
 Farooqi IS, Hopkin JM. Early childhood infection and atopic disorder. Thorax 1998 Nov; 53(11):927-32).
[189]
 McLaughlin SA, et al. Incidence of sudden infant death syndrome in Olmsted County, Minnesota: 1945 
through 1992. Mayo Clin Proc 1995 Sep; 70(9):837-43.
[190]
 Torch, WS. Diphtheria-pertussis-tetanus (DPT) immunization: a potential cause of the sudden infant death syndrome (SIDS). 
Neurology 1982; 32(4):A169 (abstract). [191]
 Torch WC. Diphtheria-pertussis-tetanus (DPT) immunization may be an unrecognized cause of sudden infant death (SIDS) and nearmiss syndrome (NMS): 12 case reports. Neurology 1986 b. (suppl 1); 36:149 (abstract). 
[192]
 Torch WC. Characteristics of diphtheria-pertussis-tetanus (DPT) postvaccinal deaths and DPT-caused sudden infant deaths syndrome 
(SIDS): a review. Neurology 1986 a (suppl 1); 36:148 (abstract). 
[193]
 Baraff LJ, et al. Possible temporal association between diphtheria-tetanus toxoid-pertussis vaccination and 
sudden infant death syndrome. Pediatr Infect Dis 1983 Jan-Feb; 2(1):7-11.
[194]
 Walker AM, et al. Diphtheria-tetanus-pertussis immunization and sudden infant death syndrome. Am J Public 
Health 1987 Aug; 77(8):945-51.
[195]
 Bakshi R, et al. Guillain-Barre syndrome after combined tetanus-diphtheria toxoid vaccination. J Neurol Sci 1997 Apr 15; 
147(2):201-2. 
[196]
 Bolukbasi O, et al. Acute disseminated encephalomyelitis associated with tetanus vaccination. Eur Neurol
1999; 41(4):231-2.
[197]
 Read SJ, et al. Acute transverse myelitis after tetanus toxoid vaccination. Lancet 1992 May 2; 339(8801):1111-2. 
[198]
 Topaloglu H, et al. Optic neuritis and myelitis after booster tetanus toxoid vaccination. Lancet 1992 Jan 18; 339(8786):178-9. 
[199]
 Schlenska GK. Unusual neurological complications following tetanus toxoid administration. J Neurol 1977 Jul 20; 215(4):299-302. 
[200]
 Baust W, et al. Peripheral neuropathy after administration of tetanus toxoid. J Neurol 1979; 222(2):131-3. 
[201]
 Fardon DF. Unusual reactions to tetanus toxoid. JAMA 1967 Jan 9;199(2):125-6. 
[202]
 Rose I. Adverse reactions to tetanus toxoid. Lancet 1973 Feb 17; 1(7799):380. 
[203]
 Sutter RW. Adverse reactions to tetanus toxoid. JAMA 1994 May 25; 271(20):1629. 
[204]
 Centers for Disease Control and Prevention. Poliomyelitis prevention in the United States: updated 
recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR 2000 May 19; 49(RR-
5):1-22.
[205]
 Ibid.
[206]
 Ibid.
[207]
www.cdc.gov/nip/vaccine/vacc-timeline.htm
[208]
 Polio, An American Story:  The Crusade that Mobilized the Nation Against the 20
th
 Century's Most Feared 
Disease p.27 
http://www.cdc.gov/ncidod/dbmd/diseaseinfo/typhoidfever_g.htm[209]
 Polio, An American Story:  The Crusade that Mobilized the Nation Against the 20
th
 Century's Most Feared 
Disease p.29 
[210]
http://www.wrongdiagnosis.com/contag/intro.htm
[211]
 Polio, An American Story:  The Crusade that Mobilized the Nation Against the 20
th
 Century's Most Feared 
Disease 
[212]
http://www.wrongdiagnosis.com/contag/intro.htm
[213]
http://www.cdc.gov/ncidod/dbmd/diseaseinfo/cholera_g.htm#How%20does%20a%20person%20get%20cholera
[214]
 Polio, An American Story:  The Crusade that Mobilized the Nation Against the 20
th
 Century's Most Feared 
Disease 
[215]
 Kinnunen E, et al. Nationwide oral poliovirus vaccination campaign and the incidence of Guillain-Barre 
Syndrome. Am J Epidemiol 1998 Jan 1; 147(1):69-73 .
[216]
 Uhari M, et al. Cluster of childhood Guillain-Barre cases after an oral poliovaccine campaign. Lancet 1989 Aug 
19; 2(8660):440-1.
[217]
 Friedrich F, et al. Temporal association between the isolation of Sabin-related poliovirus vaccine strains and the 
Guillain-Barre syndrome. Rev Inst Med Trop Sao Paulo 1996 Jan-Feb; 38(1):55-8.
[218]
 Friedrich F. Rare adverse events associated with oral poliovirus vaccine in Brazil. Braz J Med Biol Res 1997 
Jun; 30(6):695-703.
[219]
 Ibid.
[220]
 Fisher SG, et al. Cancer risk associated with simian virus 40 contaminated polio vaccine. Anticancer Res 1999 
May-Jun; 19(3B):2173-80.
[221]
 Martini F, et al. Simian-virus-40 footprints in human lymphoproliferative disorders of HIV- and HIV+ patients. 
Int J Cancer 1998 Dec 9; 78(6):669-74.
[222]
 Ibid.
[223]
 Martini F, et al. Simian virus 40 footprints in normal human tissues, brain and bone tumours of different 
histotypes. Dev Biol Stand 1998; 94:55-66.
[224]
 Martini F, et al. SV40 early region and large T antigen in human brain tumors, peripheral blood cells, and 
sperm fluids from healthy individuals. Cancer Res 1996 Oct 15; 56(20):4820-5.
[225]
 Huang H, et al. Identification in human brain tumors of DNA sequences specific for SV40 large T antigen. 
Brain Pathol 1999 Jan; 9(1):33-42.
[226]
 Bergsagel DJ, et al. DNA sequences similar to those of simian virus 40 in ependymomas and choroid plexus 
tumors of childhood. N Engl J Med 1992 Apr 9; 326(15):988-93.[227]
 Testa JR, et al. A multi-institutional study confirms the presence and expression of simian virus 40 in human 
malignant mesotheliomas. Cancer Res 1998 Oct 15; 58(20):4505-9.
[228]
 Galateau-Salle F, et al. SV40-like DNA sequences in pleural mesothelioma, bronchopulmonary carcinoma, and 
non-malignant pulmonary diseases. J Pathol 1998 Mar; 184(3):252-7.
[229]
 Lednicky JA, et al. SV40 DNA in human osteosarcomas shows sequence variation among T-antigen genes. Int 
J Cancer 1997 Sep 4; 72(5):791-800.
[230]
 Carbone M, et al. SV40-like sequences in human bone tumors. Oncogene 1996 Aug 1; 13(3):527-35.
[231]
 Rizzo P, et al. Evidence for and implications of SV40-like sequences in human mesotheliomas and 
osteosarcomas. Dev Biol Stand 1998; 94:33-40.
[232]
 Reactions of pediatricians to the recommendation for universal varicella vaccination. Newman RD, et al. Arch Pediatr Adolesc Med
1998 Aug; 152(8):792-6. 
[233]
 Prevention of varicella. Update recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR 1999 May 
28; 48(RR-6):1-5. 
[234]
Pediatric News 33(3):12, 1999. 
[235]
 Connan L, et al. Intra-uterine fetal death following maternal varicella infection. Eur J Obstet Gynecol Reprod Biol 1996 Sep; 68(1-
2):205-7. 
[236]
 Buchholz U, et al. Varicella outbreaks after vaccine licensure: should they make you chicken? Pediatrics 1999 Sep; 104(3 Pt 1):561-
3. 
[237]
 Clements DA, et al. Over five-year follow-up of Oka/Merck varicella vaccine recipients in 465 infants and adolescents. Pediatr Infect 
Dis J 1995 Oct; 14(10):874-9. 
[238]
 Johnson CE, et al. A long-term prospective study of varicella vaccine in healthy children. Pediatrics 1997 Nov; 100(5):761-6. 
[239]
 Takayama N, et al. High incidence of breakthrough varicella observed in healthy Japanese children immunized with live attenuated 
varicella vaccine (Oka strain). Acta Paediatr Jpn 1997 Dec; 39(6):663-8. 
[240]
 Bernstein HH, et al. Clinical survey of natural varicella compared with breakthrough varicella after immunization with live attenuated 
Oka/Merck varicella vaccine. Pediatrics 1993 Dec; 92(6):833-7. 
[241]
 Clements, op. cit.
[242]
 Johnson, op. cit.
[243]
 Takayama, op. cit.
[244]
 Halloran ME, et al. Theoretical epidemiologic and morbidity effects of routine varicella immunization of preschool children in the 
United States. Am J Epidemiol 1994 Jul 15; 140(2):81-104. [245]
 Gershon AA, et al. Varicella vaccine: the American experience. J Infect Dis 1992 Aug; 166 Suppl 1:S63-8.
[246]
 Plotkin SA, et al. Zoster in normal children after varicella vaccine. J Infect Dis 1989 May; 159(5):1000-1. 
[247]
N Engl J Med, September 11, 1989, p. 1333.
[248]
 Fisher, Barbara Loe. The Consumer's Guide to Childhood Vaccines, National Vaccine Information Center, 
Vienna, VA, 1997.
[249]
 Freed GL, Bordley WC, Clark SJ, Konrad TR. Family physician acceptance of universal hepatitis B 
immunization of infants. J Fam Pract 1993 Feb; 36(2):153-7.
[250]
 Ibid.
[251]
 Kinnersley P. Attitudes of general practitioners towards their vaccination against hepatitis B. BMJ 1990 Jan 27; 
300(6719):238.
[252]
 Burden AD, et al. Poor uptake of hepatitis B immunization amongst hospital-based health care staff. Postgrad 
Med J 1991 Mar; 67(785):256-8.
[253]
 Freed GL, et al. Family physician acceptance of universal hepatitis B immunization of infants. J Fam Pract
1993 Feb; 36(2):153-7.
[254]
 Niu MT, Davis DM, Ellenberg S. Recombinant hepatitis B vaccination of neonates and infants: emerging 
safety data from the Vaccine Adverse Event Reporting System. Pediatr Infect Dis J 1996 Sep; 15(9):771-6.
[255]
 Statement of the Association of American Physicians and Surgeons on Vaccines: Public Safety and Personal 
Choice before the Committee on Government Reform and Oversight U.S. House of Representatives. From 
www.aapsonline.org/aaps/
[256]
 Incao, Philip, M.D. Letter to Representative Dale Van Vyven, Ohio House of Representatives. March 1, 1999. 
Provided to www.garynull.com by The Natural Immunity Information Network.
[257]
 Dunbar B. Hearing before the Subcommittee on Criminal Justice, Drug Policy and Human Resources of the 
House Government Reform Committee. May 8, 1999, transcript by Federal News Service.
[258]
 Hadler SC, et al. Long-term immunogenicity and efficacy of hepatitis B vaccine in homosexual men. N Engl J 
Med 1986 Jul 24; 315(4):209-14.
[259]
 Pasko MT, et al. Persistence of anti-HBs among health care personnel immunized with hepatitis B vaccine. Am 
J Public Health 1990 May; 80(5):590-3.
[260]
 Encephalitis after hepatitis B vaccination: recurrent disseminated encephalitis or MS? Neurology 1999 Jul 22; 
53(2):396-401.[261]
 Herroelen L, et al. Central-nervous-system demyelination after immunisation with recombinant hepatitis B 
vaccine. Lancet 1991 Nov 9; 338(8776):1174-5.
[262]
 Viral Hepatitis Prevention Board. Hepatitis B vaccine and central nervous system demyelinating diseases. 
Pediatr Infect Dis J 1999 Jan; 18(1):23-4. Review.
[263]
 Nadler JP. Multiple sclerosis and hepatitis B vaccination. Clin Infect Dis 1993 Nov; 17(5):928-9.
[264]
 Hall A, et al. Multiple sclerosis and hepatitis B vaccine? Vaccine 1999 Jun 4; 17(20-21):2473-5.
[265]
 Birley HD, et al. Hepatitis B immunisation and reactive arthritis. BMJ 1994 Dec 3; 309(6967):1514.
[266]
 Pope JE, et al. The development of rheumatoid arthritis after recombinant hepatitis B vaccination. J Rheumatol
1998 Sep; 25(9):1687-93.
[267]
 Bracci M, et al. Polyarthritis associated with hepatitis B vaccination. Br J Rheumatol 1997 Feb; 36(2):300-1.
[268]
 Hachulla E, et al. Reactive arthritis after hepatitis B vaccination. J Rheumatol 1990 Sep; 17(9):1250-1.
[269]
 Vautier G, et al. Acute sero-positive rheumatoid arthritis occurring after hepatitis vaccination. Br J Rheumatol
1994 Oct; 33(10):991.
[270]
 Grotto I, et al. Major adverse reactions to yeast-derived hepatitis B vaccines-a review. Vaccine 1998 Feb; 
16(4):329-34.
[271]
 Vaccinations: how safe and how effective, Nexus, August-September, 1993, p. 64. 
[272]
 Scheibner, Viera. Vaccination: 100 Years of Orthodox Research Shows that Vaccines Represent a Medical 
Assault on the Immune System, Maryborough, Victoria, Australia, Australian Print Group, 1993, p. 86-9.
[273]
 Fiumara NJ, Etking PH. Mumps outbreak in Westwood, Massachusetts - 1981. Epidemiologic notes and 
reports. MMWR 1982; 33(29):421-30.
[274]
 Ibid.
[275]
 Cherry JD. The 'new' epidemiology of measles and Rubella. Hosp Practice 1980 Jul; 15(7):49-57.
[276]
 Gustafson TL, et al., Measles outbreak in a fully immunized secondary-school population. NEJM 1987; 
316(13):771-4.
[277]
 Miller, Neil Z. Immunization Theory vs. Reality, The Atlantean Press, Santa Fe, NM, 1996, p. 82.
[278]
 Scheibner, op. cit., p. 111.
[279]
 Cherry, op. cit.[280]
 Fulginiti VA, et al. Altered reactivity to measles virus. Atypical measles in children previously immunized with 
inactivated measles virus vaccines. JAMA 1967; 202(12):1075-80. 
[281]
 Scott TF, Bonanno DE. Reactions to live-measles-virus vaccine in children previously inoculated with killed 
virus vaccine. N Engl J Med 1967; 277(5):248-51.
[282]
 Rauh JL, et al. Rubella surveillance and vaccination at adolescence. American Journal Dis Child 1972; 124:27-
8. 
[283]
 Howson CP, Fineberg HV. Adverse events following pertussis and rubella vaccines. summary of a report of the 
institute of medicine. JAMA 1992; 267(3):392-6. 
[284]
 Markowitz LE, Preblud SR, Orenstein WA, Rovira EZ, Adams NC, Hawkins CE, Hinman AR. Patterns of 
transmission in measles outbreaks in the United States, 1985-1986. N Engl J Med 1989; 32:75-81.
[285]
JAMA 1990 May 9; 263:2467-71.
[286]
MMWR 1989; 38:329-30. 
[287]
 National Health Federation Bulletin, November 1969.
[288]
 Gary Null Interview with Jamie Murphy, December 18, 1997.
[289]
 Murphy, Jamie. What Every Parent Should Know About Childhood Immunization, Boston, Earth Healing 
Products, 1993, p. 114.
[290]
 Gary Null Interview with Jamie Murphy, April 7, 1995.
[291]
 Scheibner, op. cit., p. 38.
[292]
 Gary Null Interview with Meryl Dorey, December 17, 1997. 
[293]
 Sawada H, Yano S, Oka Y, Togashi T. Transmission of Urabe mumps vaccine between siblings. Lancet 1993 
Aug 7; 342(8867):371.
[294]
 Scheibner, op. cit., p. 92.
[295]
Sawada, op. cit.
[296]
Dorey M. The Australian Vaccination Network Newsletter, November 1997.
[297]
British Medical Journal, July 4, 1987.
[298]
http://www.cdc.gov/nip/vaccine/vacc-timeline.htm[299]
 Poland GA, et al. Failure to reach the goal of measles elimination. Apparent paradox of measles infections in 
immunized persons. Arch Intern Med 1994 Aug 22; 154(16):1815-20.
[300]
 Miller E, et al. Antibodies to measles, mumps and rubella in UK children 4 years after vaccination with 
different MMR vaccines. Vaccine 1995 Jun; 13(9):799-802.
[301]
 Whittle H, et al. Poor serologic responses five to seven years after immunization with high and standard titer 
measles vaccines. Pediatr Infect Dis J 1999 Jan; 18(1):53-7.
[302]
 Maldonado YA, et al. Early loss of passive measles antibody in infants of mothers with vaccine-induced 
immunity. Pediatrics 1995 Sep; 96(3 Pt 1):447-50.
[303]
 Wong RD, et al. Clinical and laboratory features of measles in hospitalized adults. Am J Med 1993 Oct; 
95(4):377-83.
[304]
 Auwaerter PG, Hussey GD, Goddard EA, Hughes J, et al. Changes within T cell receptor V beta subsets in 
infants following measles vaccination. Clin Immunol Immunopathol 1996 May; 79(2):163-70.
[305]
 Ward BJ. Changes in cytokine production after measles virus vaccination: predominant production of IL-4 
suggests induction of a Th2 response. Clin Immunol Immunopathol 1993 May; 67(2):171.
[306]
 RESPONSE TO W.H.O. EVIDENCE FOR VACCINE SAFETY AND EFFECTIVENESS 
Trevor Gunn, BSc, RSHom 
[307]
 U.S. government statistic http://www.hhs.gov/news/press/pre1995pres/910000a.txt
[308]
 E. Holt, et al from the Journal of Pediatrics, Vol. 85, No 2 pp188-194, February 1990   
[309]
 (The lancet April 4, 1981 765). 
[310]
 , P. Aby, et Al, Pediat Infec DisJ 8: 197-200, 1989
[311]
 Clemens et al, American Journal of Epidemiology, Vol 128, No. 6 1330-39
[312]
MMWR Morb Mortal Wkly Rep 1996 Sep 6; 45(RR-12):1-35.
[313]
 Cheek JE, et al. Mumps outbreak in a highly vaccinated school population. Evidence for large-scale 
vaccination failure. Arch Pediatr Adolesc Med 1995 Jul;149(7):774-8.
[314]
 Briss PA, et al. Sustained transmission of mumps in a highly vaccinated population: assessment of primary 
vaccine failure and waning vaccine-induced immunity. J Infect Dis 1994 Jan; 169(1):77-82.
[315]
 Hersh BS, et al. Mumps outbreak in a highly vaccinated population. J Pediatr 1991 Aug; 119(2):187-93.
[316]
 Zimmermann H, et al. Mumps epidemiology in Switzerland: results from the Sentinella surveillance system 
1986-1993. Sentinella Work Group. German. Soz Praventivmed 1995; 40(2):80-92.[317]
 Matter L, et al. The incidence of rubella virus infections in Switzerland after the introduction of the MMR mass 
vaccination programme. Eur J Epidemiol 1995 Jun; 11(3):305-10.
[318]
 Hillary IB, et al. Persistence of rubella antibodies 15 years after subcutaneous administration of Wistar 27/3 
strain live attenuated rubella virus vaccine. JAMA 1981 Feb 20; 245(7):711-3.
[319]
 Scheibner, op. cit., p. 111.
[320]
Cherry, op. cit., 49-57. 
[321]
 Howson CP, Fineberg HV. Adverse events following pertussis and rubella vaccines. summary of a report of the Institute of Medicine. 
JAMA 1992; 267(3):392-6. 
[322]
 Davis RL, et al.  MMR2 immunization at 4 to 5 years and 10 to 12 years of age: a comparison of adverse 
clinical events after immunization in the Vaccine Safety Datalink project. The Vaccine Safety Datalink Team. 
Pediatrics 1997 Nov; 100(5):767-71.
[323]
 Miller D, et al. Measles vaccination and neurological events. Lancet 1997 Mar 8; 349(9053):730-1.
[324]
 Sackey AH, et al. Hemiplegia after measles, mumps, and rubella vaccination. BMJ 1993 May 1; 
306(6886):1169.
[325]
 Kazarian EL, et al. Optic neuritis complicating measles, mumps, and rubella vaccination. Am J Ophthalmol 
1978 Oct; 86(4):544-7.
[326]
 Kline LB, et al. Optic neuritis and myelitis following rubella vaccination. Arch Neurol 1982 Jul; 39(7):443-4.
[327]
 Akobeng AK et al. Inflammatory bowel disease, autism, and the measles, mumps, and rubella vaccine.  J 
Pediatr Gastroenterol Nutr 1999 Mar; 28(3):351-2.
[328]
 Chiba Y, et al. Abnormalities of cellular immune response in arthritis induced by rubella vaccination. J 
Immunol 1976 Nov; 117(5 Pt 1):1684-7.
[329]
 Tingle AJ, et al. Postpartum rubella immunization: association with development of prolonged arthritis, 
neurological sequelae, and chronic rubella viremia. J Infect Dis 1985 Sep; 152(3):606-12.
[330]
 Roberts RJ, et al. Reasons for non-uptake of measles, mumps, and rubella catch up immunisation in a measles 
epidemic and side effects of the vaccine. BMJ 1995 Jun 24; 310(6995):1629-32.
[331]
http://165.112.6.70/exhibition/smallpox/sp_threat.html
[332]
http://165.112.6.70/exhibition/smallpox/sp_variolation.html
[333]
 Miller, Neil Z. Immunization Theory vs. Reality, Santa Fe, NM, The Atlantean Press, 1996. 
[334]
 E. Jenner, Inquiry into the Causes and Effects of the Variolae Vaccine (London: Sampson Low, 1798) Case XVII [335]
 E. Jenner, Inquiry into the Causes and Effects of the Variolae Vaccine, p. 45. 
[336]
 summary of his practice in Bohn's Handbuch der Vaccination.   Leipzig, 1875, p. 82. 
[337]
 C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 6 p. 137-138 
[338]
 E. Jenner, Inquiry into the Causes and Effects of the Variolae Vaccine, Case III 
[339]
 Salmade, La Pratique de I'Inoculation. Paris, An. vii. (1798) p. 51. 
[340]
 C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 2 p. 41. 
[341]
 J. Baron, Life of Jenner, i. p. 48. 
[342]
 C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 2 p. 23. 
[343]
 C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 2 p. 26.  
[344]
 C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 2 p. 31. 
[345]
 C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 5 p. 123 
[346]
Contributions to Physical and Medical Knowledge, 1799 , p. 387. 
[347]
 C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 1 p. 8. 
[348]
 C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 1 p. 11. 
[349]
 C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 6 p. 150 
[350]
 E. Jenner, Inquiry into the Causes and Effects of the Variolae Vaccine, general observations section of conclusion 
[351]
 J. Baron, Life of Jenner, ii. P304. 
[352]
 C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 6 p. 153- 154 
[353]
 House of Commons, 17th June, 1840.  
[354]
 C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 14 p. 339-340.  
[355]
Parliamentary Papers, vol. ci., 1852-53. 
[356]
 C. Ruata, A Summary of the Proofs That Vaccination Does Not Prevent Small-pox but Really Increases It (National Anti-Vaccination 
League S616: 1904) p. 8. 
[357]
 C. Ruata, A Summary of the Proofs That Vaccination Does Not Prevent Small-pox but Really Increases It (1904) p. 10. 
[358]
 C. Ruata, A Summary of the Proofs That Vaccination Does Not Prevent Small-pox but Really Increases It (1904) p. 10~11. 
[359]
 C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 14 p. 350 [360]
Encyclopedia Britannica, Ninth Edition, 1888. subject: Vaccination, section: Influence of vaccination upon smallpox.Chart. 
[361]
 C. Ruata, A Summary of the Proofs That Vaccination Does Not Prevent Small-pox but Really Increases It (1904) p. 16~17. 
[362]
http://www.informedchoice.info/cocktail.html
[363]
http://www.bt.cdc.gov/agent/smallpox/vaccination/live-virus.asp
[364]
http://165.112.6.70/exhibition/smallpox/sp_eradicate.html
[365]
http://www.cdc.gov/nip/vaccine/vacc-timeline.htm
[366]
 Ibid.  
[367]
 Intussusception Among Recipients of Rotavirus Vaccine-United States, 1998-1999. MMWR 1999 July 16; 48(27);577-81. 
[368]
 Rosenthal S, et al. The reporting sensitivities of two passive surveillance systems for vaccine adverse events. Am J Public Health
1995; 85:1706-9. 
[369]
http://www.rotavirusvaccine.org/documents/RotaShield_Fact_Sheet_CDC.pdf.
[370]
 Michael Devitt, CDC Calls for Suspension of Childhood Rotavirus Vaccine "No One Should Now Be Giving 
Rotavirus Vaccine to Anyone." Dynamic Chiropractic October 4, 1999, Volume 17, Issue 21 
http://www.chiroweb.com/archives/17/21/04.html
[371]
 Parry, British Medical Journal, December 1, 1928, p.116.
[372]
 Landrigan PJ, Witte JJ. Neurologic disorders following live measles-virus vaccination. JAMA 1973; 
223(13):1459-62. 
[373]
 Pollock TM, et al. Symptoms after Primary Immunisation with DPT and with DT Vaccine. Lancet 1984 July; 
21:146-9. 
[374]
 Hirtz DG, et al. Seizures Following Childhood Immunizations. Journal of Pediatrics 1983; 102(12):14-8. 
[375]
 Goldwater PN, et al. Sudden infant death syndrome: a possible clue to causation. Medical Journal Aust 1990; 
153:59-60. 
[376]
 Goldwater PN, et al. Sudden infant death syndrome: a possible clue to causation. Medical Journal Aust 1990; 
153:21-5.
[377]
 Denborough MA, et al. Malignant Hyperpyrexia and Sudden Infant Death. Lancet 1982 Nov 13: 1068-72.
[378]
 Chaitow, Leon. Vaccination and Immunization: Dangers, Delusions & Alternatives, Beekman Publishing, 
1996.
[379]
 Gary Null Report, November 15, 1994.[380]
 Coulter, Harris L and Fisher, Barbara Loe. A Shot in the Dark, Garden City Park, NY, Avery, 1991. 
[381]
 Merritt HH. Textbook of Neurology, Sixth Edition, Philadelphia, Lea and Febiger, 1979, p. 160.
[382]
 Phillips, Alan. Vaccination: dispelling the myths. Nexus, October-November 1997.
[383]
 National Technical Information Service, Springfield, VA. 
[384]
 Scheibner, Viera. Vaccination: 100 Years of Orthodox Research Shows that Vaccines Represent a Medical 
Assault on the Immune System, Maryborough, Victoria, Australia, Australian Print Group, 1993.
[385]
 Torch WC. Diphtheria-pertussis-tetanus (DPT) immunization: a potential cause of the sudden infant death 
syndrome (SIDS). Neurology 1982; 32(4). 
[386]
 Scheibner, op. cit., p. 62.
[387]
 Bafaff L, et al. Possible temporal association between diphtheria-tetanus toxoid-pertussis vaccination and 
sudden infant death syndrome. Pediatric Infectious Dis, 2, 1983, p. 7.
[388]
 James, Walene. Immunization: The Reality Behind the Myth, Massachusetts, Bergin & Gervey, 1988.
[389]
 Cournoyer, Cynthis. What About Immunizations?, 6
th
 Edition, Nelson's Books, 1995, p. 34.
[390]
Immunization, Special Edition, Santa Fe, NM, Mothering Publications, 1984.
[391]
 Moskowitz R. The Case Against Immunizations, Washington, DC, National Center for Homeopathy.
[392]
 Cournoyer, op. cit., p. 35.
[393]
 Scheibner, op. cit., p. 88-9.
[394]
 Black FL, et al. Inadequate Immunity to Measles Immunity in Era of Vaccine-Protected Mothers. Bull WHO
1984; 62(92):315-9.
[395]
 Lennon JL, Black FL. Maternally derived measles immunity in era of vaccine-protected mothers. Journal of 
Pediatrics 1986; 108(1):671-6.
[396]
 Scheibner, op. cit., p. 199.
[397]
 Aaby P, et al. Long-term survival after Edmonston-Zagreb measles vaccination in Guinea-Bissau: increased 
female mortality rate. J Pediatr 1993 Jun; 122(6):904-8.
[398]
 Garenne M, et al. Child mortality after high-titre measles vaccines: prospective study in Senegal. Lancet 1991 
Oct 12; 338(8772):903-7.
[399]
 Cournoyer, op. cit., p. 160.[400]
 "Interview with Barbara Loe Fisher." National Vaccine Information Center Newsletter Website.
[401]
 Cournoyer, op. cit., p. 156.
[402]
 The National Childhood Vaccine Injury Act of 1986 Public Law 99-690, The Compensation System and How 
it Works. The National Vaccination Information Center, Vienna, VA, 1990.
[403]
 Vaccine injury compensation program statistics. NVIC News, August 1994, p. 10.
[404]
 Phillips, op. cit.
[405]
 National Vaccine Injury Compensation Program, Health Resources and Services Administration, Rockville, 
MD.
[406]
 Neustaedter R. Do vaccines disable the immune system? Internet Document.
[407]
 Fisher, Barbara Loe. The Consumer's Guide to Childhood Vaccines, Vienna, VA, National Vaccine 
Information Center, 1997.
[408]
 Ibid, p. 48.
[409]
 Ibid, p. 64.
[410]
 National Vaccine Injury Compensation Program: monthly statistics report, September 30, 2002. U.S. 
Department of Health and Human Services, Health Resources and Services Administration. From 
www.hrsa.gov/osp/vicp/monthly.htm.
[411]
 Gary Null Interview with Barbara Loe Fisher, April 11, 1995.
[412]
 Ibid.
[413]
 Gary Null Interview with Dr. Dean Black, April 7, 1995. 
[414]
 Gary Null Interview with Curtis Cost, December 17, 1997.
[415]
 Gary Null Interview with Barbara Loe Fisher, April 11, 1995.
[416]
 Gary Null Interview with Alan Phillips, December 17, 1997.
[417]
 Gary Null Interview with Dr. Dean Black, April 7, 1995. 

Vaccination: Pain, Profit, and Politics - Part 1By Gary Null, Ph.D., and Martin Feldman, M.D. Today we have a major controversy brewing in the U.S. healthcare field.  The question is being asked if the vaccinations that we are giving our children are safe and effective.  What is the proof that vaccinations are safe?  We have undertaken an enormous job of reviewing the world literature to examine whether vaccinations are safe, and whether they are effective. We have taken an in depth look at the politics, the economic incentives, and the conflicts of interest involved in the politics of vaccinations. We have reviewed the scientific literature and we have examined the results on the people who have received vaccinations and the health effects of these (often mandated) medical procedures. We have examined here the myths versus the facts in the science of vaccines, and whether the procedures themselves represent good science or whether the manufacturers and physicians who provide them support conjecture or good scientific practice.  We have examined the lobbying on behalf of the vaccine makers, and we have examined the safety and efficacy of the dozens of vaccinations that children are receiving in the first months of life.  Our society rarely looks at the safety and efficacy of medical manufactures which have enormous power to  influence the decisions of the CDC, the FDA, and the Institutes of Allergy and Infectious Disease[1] [2] [3] [4] [5] [6] [7] [8] [9] [10], but the media rarely hears of the trajedies and the side effects.  We do, however, hear that vaccines promise to prevent some new condition, (such as genital warts.[11] [12] [13]) However, we have innundated the developing baby's body with dozens of vaccines[14], but no industry advisor or anyone in the FDA has ever suggested that this is too much. We are overwhelming the child's system with adverse effects, and all this has happened in the last 40 years. Let us now examine the truth:Life Expectancy in the 20th Century When we take a look at the article by David R. Francis, entitled, "Why do Death Rates Decline"[15], to get a general idea about how vaccinations might play a role in general health throughout the 20th century, we see that mortality rates decline steadily but rapidly throughout the 20th century.  Using this logic, vaccine advocates might wonder why increased rates of vaccination in the past two decades wouldn't have made mortality rates decrease faster than in the first half of the century. However, we learn that:  "During the twentieth century, mortality rates declined quite rapidly in the United States and in all developed countries. Except for a 10-year period between 1955 and 1965 when the mortality rate was essentially flat, mortality rates have declined at the relatively constant rate of approximately 1 to 2 percent per year since 1900.[16]"   If vaccines were the cause of the decline of disease, then shouldn't the rates of mortality have declined more rapidly in the latter half of the 20th century, with the use of more and more required vaccinations? The second point that Francis makes is that in the second half of the 20th century, the most mortality decline occurred in people who were in mid- life.  Vaccine advocates might argue that mortality rates ought to have declined more quickly in very young and school aged children:  "In the latter four decades of the century, about two-thirds of life expectancy improvements resulted from mortality reductions for those over age 45.[17]"Thus, the most improvements in terms of mortality in the second half of the 20th century occurred in people beyond the age of childhood vaccinations. The third point that the author makes is self explanatory:  improved nutrition and public health measures in children were more important than medical intervention in 1900.  This was the height of the measles outbreak.  In addition, "Infectious diseases were the leading cause of death in 1900, accounting for 32 percent of deaths. Pneumonia and influenza were the biggest killers. Therefore, improved nutrition and public health measures, particularly important for the young, were vastly more important in this period than medical interventions.[18]"The fourth point Mr. Francis makes is that in the mid 20th century, penicillin, sulfa drugs, and antibiotics contributed to a mortality decline in children:  "Between 1940 and 1960, infectious diseases as a cause of death continued to decline. But more of this decline was attributable to medical factors, such as the use of penicillin, sulfa drugs (discovered in 1935), and other antibiotics. These help the elderly as well as the young, thereby reducing mortality across the age spectrum. By 1960, 70 percent of infants could be expected to survive to age 65.[19]"Vaccinations were not mentioned in this paragraph. The fifth important point of Mr. Francis is that smoking habits of Americans is an important factor in reducing mortality rates throughout the 20th century. The important issue to note here is that smokers generally begin their habit well after vaccination schedules have been completed, and that smoking causes a huge health risk despite vaccinations received:"Smoking cessation and better diets also are factors in [mortality decrease]: per capita consumption of cigarettes rose from essentially zero in 1900 to more than 4,000 per year per capita in 1960, or over two packs per smoker per day. Since then, per capita consumption has fallen by more than 50 percent. These trends affect death from heart disease and from smoking-sensitive cancers with a 10 to 20-year lag.[20]"Trevor Gunn, a biochemist in England,  claims that immunity from vaccination is shorter lived than natural immunity provided by the illness itself.  First, a child may contract an illness in adulthood for which it was vaccinated in childhood, and second, a mother may not be able to impart immunity provided by vaccination as easily as the immunity she developed over the course of her natural life. [21]According to a leaflet by the CDC, figures of average morbidity by various illnesses were reduced as a result of vaccination according to the flyer entitled,"What would happen if we stopped vaccinations?[22]"  The leaflet, however, does not include information on the other public health measures that coalesced to provide increased public health in the 20th century as well.A detailed review of morbidity and illness factors in Union Soldiers in the Civil war illustrates that the onset of what we think of now as 'old age' illnesses occurred in much younger men during the 19th century, but improved throughout the 20th century: "chronic illnesses affected young and middle aged men to a much greater degree in the past than today.  [In a study of two cohort groups of Union Soldiers] one quarter of men aged 20-24 and over half of men aged 35-39 were rejected as unfit to serve due to illnesses such as cardiovascular disease and hernias.  Similarly, elderly men were more likely to suffer from chronic conditions than in the past...Of men aged  60-64 during the 1890-1910 period, 90% suffered from a chronic condition, as compared to 75% of same aged men in 1994.[23]"For example, for two of the conditions studied that we know now to be related to inflammation[24] [25] [26] [27]and stress[28] (particularly as results from diet[29] [30] [31] [32] [33] [34] [35] [36] [37] [38]and lifestyle[39] [40] [41] [42] [43]), that is, heart disease and arthritis, we see that the average age for onset for the 1830-1845[44]cohort was approximately 56 years of age, whereas the average age of onset for the 1918-1927 cohort was approximately 66 years[45], or a difference of 10 years in the age of onset in the later group.  Similarly, for the arthritis sample, the average age of onset for the 1830-1845 cohort was approximately 54 years whereas the later cohort was approximately 65 years[46] .  So we see that as time goes on, at least two public health markers were improved greatly in the 20th century; the age of onset of chronic disease in the forms of heart disease and arthritis was increased considerably.  These health factors, too, were improved without the help of vaccinations.[47] [48] [49] [50](We will discuss this assertion later in this paper)For more than a hundred years, however, two basic assumptions have been put forth by public health officials. One is that vaccines are safe.[51] [52]The second is that vaccines are effective for the conditions for which they're given.[53] The public and our legislators have, by and large, accepted these assumptions as true, and as a result it is now compulsory in many states that children have as many as 20 [54] [55]separate inoculations before entering school, or 33 by the time they are finished with secondary education. Some of these are given as early as the first few weeks of life.[56]We've been told that the end of polio, for example, as a serious health threat is due to mass inoculation programs[57] [58], and again we have accepted the official dogma without question. But as we shall see, this is not exactly the truth.[59] What's more, a disturbing reality that generally has gone unrecognized is the ever-growing number of people suffering adverse reactions to vaccinations[60]. These individuals are predominantly infants and children, and the problems they've incurred as a result of vaccination go far beyond sore arms and transitory fever: Conditions such as autism, attention deficit disorder, minimal brain dysfunction, and other biochemical and neurological abnormalities have been linked to the effects of vaccines[61]. Most tragically, so has SIDS-sudden infant death syndrome.[62][63]Although the government agencies such as the CDC[64], the National Institutes of allergy and infectious disease [65] [66], among others[67] [68] [69] [70], have tried to debunk a possible link between the proximity of vaccinations and untimely deaths of children in the first few months of life, we cite the government's involvement in supporting the cigarette industry in the first half of the 20th century[71] [72], and the widespread use of pesticide. The government also touted the benefits of hormone replacement therapy until 2002[73] [74], for which women are now suffering breast cancer[75] [76], stroke[77], and dementia[78]; the government does not have a good track record on the issue of dangerous NSAIDS such as Vioxx[79], for the use of which over 100,000 deaths are attributed[80].  As a result, the fact that we do not accept the government data on this issue does not mean that we are slanted, but it means that we are careful to point out the differences between the data that is reported and what the government deems is true.  We examine the government's point of view on SIDS on page 18 of this paper.  Because of underreporting of these troubling statistical links[81] [82] [83],however, a full picture of the effects of vaccination has not emerged. The problem of underreporting is a deep-seated one[84]. Yet the official line is that a small minority must accept negative consequences for the greater good of the majority.This investigation is an attempt to uncover the truth. In three parts, we will discuss facts that challenge our assumptions about vaccine safety and effectiveness, look at the effects associated with specific vaccines, and summarize some of the legal, political and economic issues surrounding the use of vaccines. The series has required a review of thousands of articles. We are presenting information based upon hard science; hundreds of references are included here for those who want to read further. For people challenging mandatory vaccination policies, the reference section will be particularly helpful.Why We Should Question Our AssumptionsWe think of vaccinations as panaceas and look to science to develop new ones for every known affliction, from the common cold to AIDS. Jamie Murphy, author of What Every Parent Should Know About Childhood Immunization,[85]attributes society's general acceptance of vaccinations, in large part, to state laws that dictate children must receive vaccines before they can attend school.     However, we must take a close look at our assumptions and ask, are we seeing the full picture? The reasons we should challenge our beliefs include the following:Safety issues. Significant adverse effects have been reported with every type of vaccine [86] [87]. These reactions can occur soon after vaccination (short-term reactions) or several months to years later (long-term)[88]. Delayed reactions are more insidious and less obviously linked to vaccination, and thus necessitate largescale epidemiological studies to be proven.One would think that before injecting children worldwide with hundreds of millions of doses of vaccines, enough clinical trials would be performed to determine exactly what the effects of this large-scale human genetic experiment would be. Lack of funding is not the problem. Each year, more than $1 billion[89][90] is appropriated by Congress to federal health agencies to develop, purchase, and promote the mass use of vaccines in the U.S. but not to fund independent researchers to investigate vaccine-related health problems.In the meantime, as an example of the volume of adverse reactions reported to the Vaccine Adverse Event Reporting System (VAERS), there were 38,787 such events between 1991 and 1994. Of these, 45 percent occurred on the day of vaccination, 20 percent on the following day, and 93 percent within two weeks of vaccination. Deaths were most prevalent in children 1 to 3 months old and were defined as sudden infant deaths. (The author of the paper makes it clear that, "sudden infant death syndrome has not been associated with vaccination."[91] Since, as has been amply documented, only one-tenth of vaccine-induced reactions are reported to the VAERS (by some estimates, this is figure is even greater)[92],[93], this number vastly underestimates the real incidence of vaccine-associated complications. Furthermore, no link has been established when the adverse event occurs long after the time of vaccination[94].  In fact, a 1998 study in the Lancet and a recent review claim that no link exists between the MMR vaccine and subsequent long-term health events such as autism or bowel obstruction.[95] [96] [97]Another area of concern is that many doctors refuse to vaccinate themselves and their families,  [98] [99] [100]even though physicians belong to a high-risk category and are urged to accept vaccinations because of their continued exposure to infectious disease. A 1981 article in the Journal of the American Medical Association reports that the lowest vaccination rate among medical personnel for the German measles vaccine occurred among obstetrician/gynecologists and the next lowest rate occurred among pediatricians.  [101] The authors conclude, "The fear of unforeseen vaccination reactions was the main reason for the low uptake rate of physicians to be vaccinated." In the British Medical Journal, a 1990 article tells us that of 598 doctors questioned about hepatitis B vaccine, 86 percent believe that all general practitioners should be vaccinated against this disease. Yet 309 of those practitioners had not been vaccinated themselves. [102] [103]  A 2004 article in the Journal of Occupational Medicine summarizes these findings, and others, including the fact that some doctors are unconcerned with regards to vaccination protection, while in that over 80% received Hep B inoculation, only 49% confirmed immune response to the virus, and only half did any preventive measures after needle stick injuries.[104]Vaccinations Are Based on Unsound Principles. According to Jamie Murphy, "Vaccines are portrayed as being indispensable and somehow better at disease protection than what our innate biological defenses and nutritional resources have accomplished for thousands of years.... Before the introduction of the measles and mumps vaccines, children got measles and they got mumps, and in the great majority of cases those diseases were benign."[105]Walene James, author of Immunization: The Reality Behind the Myth,[106]believes that the full inflammatory response is necessary to create real immunity.[107] James summarizes the work of Dr. Richard Moskowitz, past president of the National Institute of Homeopathy, as stating, "'Vaccines trick the body so that it will no longer initiate a generalized inflammatory response. They thereby accomplish what the entire immune system seems to have evolved to prevent. They place the virus directly into the blood and give it access to the major immune organs and tissues without any obvious way of getting rid of it. These attenuated viruses and virus elements persist in the blood for a long time, perhaps permanently. This, in turn, implies a systematic weakening of the ability to mount an effective response, not only to childhood diseases but to other acute infections as well.'"Murphy observes that vaccines, unlike childhood diseases, do not produce permanent immunity. "The medical profession does not know how long vaccine immunity lasts because it is artificial immunity. If you get measles naturally, in 99 percent of the cases, you have lifelong immunity. If you have German measles you will have lifelong immunity. The chances of getting measles twice, German measles twice, or even whooping cough twice [are remote].... However, if you get a measles vaccine or a DPT vaccine, [it does not give you 100% assurance]  that the vaccine will prevent you from getting the disease." [108]     In "Vaccination: Dispelling the Myths," Alan Phillips writes, "The clinical evidence for vaccination is their ability to stimulate antibody production in the recipient, a fact which is not disputed. What is not clear, however, is whether or not such antibody production constitutes immunity. For example, a-gamma globulinemic children are incapable of producing antibodies, yet they recover from infectious diseases almost as quickly as other children....Natural immunization is a complex phenomenon involving many organs and systems; it cannot be fully replicated by the artificial stimulation of antibody production....[Our] immunological reserves may thus actually be reduced, causing a generally lowered resistance."[109] [110]     Phillips adds: "Another component of immunization theory is 'herd immunity,' ...when enough people in a community are immunized, all are protected.... there are many documented instances showing just the opposite-fully vaccinated populations do contract diseases; with measles, this actually seems to be the direct result of high vaccination rates...."[111], [112] [113]Writing in Nexus, Phillips makes the point that immunization practice assumes that all children, regardless of age and size, are virtually the same. "An 8-pound 2-month-old receives the same dosage as a 40-pound five-year-old," Phillips points out. "Infants with immature, undeveloped immune systems may receive five or more times the dosage (relative to body weight) as older children." What's more, random testing has revealed that the number of "units" within doses has been found to range up to three times what the label indicates, with quality control tolerating a rather large margin of error.Questionable Science. Many scientific studies tell us that vaccines are safe and effective when this is not necessarily the case. 110 112 113Doctors and vaccine proponents often quote studies done solely on antibody production in the blood, not taking into account clinical experiences.  We must note, however, that clinical experience is important, and particularly with regards to the treatment of viral infections that have not or cannot be treated at the time with vaccine.  For example, we know that transmission at the time of birth of the chickenpox virus is dangerous to the livelihood of the infant, and that low birth weight contributes to susceptibility to death from the virus[114], thus indicating a possible need for doctors to be clinically aware of the mother's risk factors for low birth weight infants[115] [116].  For example doctors recommend the following for the outcome of a healthy birth weight including no alcohol consumption, drug use, and adequate nutrition[117] as well as regular prenatal checkups[118] .  In addition to being aware of the causes of low birth weight infants, the use of the antibody titer VZIG in a timely manner can sometimes prevent death[119].  As opposed to the chickenpox vaccine (which contains live, attenuated chickenpox virus), VZIG contains immune fractions from the blood of people that can help those who are dangerously immune compromised for a short period of time[120].  Other non-vaccine alternatives are being made available for this widespread virus; the use of acyclovir, which has been determined to be useful in lessening the severity of chickenpox infection in children, might be preferable to the VZIG treatment (we note that VZIG does contain the preservative thimerosol[121]), but the use of acyclovir during pregnancy has not yet been widely tested[122] in the clinical setting, and shows that much more research is needed in non vaccine alternatives.Dr. Dean Black, author of Immunizations: Compulsion or Choice, brings up an issue that needs more attention-what if we stopped compulsory vaccination? "By looking at what happens in countries where vaccinations are no longer required," he says, "we can get an idea of what would truly happen if we were to cease demanding compulsory immunization in America. In 1975, Germany stopped requiring pertussis [whooping cough] vaccinations, and the number of children vaccinated promptly began to drop. Today, it has dropped to well below 10 percent. What has happened in Germany from pertussis over that period of time? The mortality rate has continued to decrease."[123]The Natural Evolution of Disease. Immunization supposedly puts an end to disease. We attribute the decline in polio to the polio vaccine, the "disappearance" of smallpox to the smallpox vaccine, and so forth.[124], [125], [126], [127], [128], [129]But are vaccinations the magic bullets we believe them to be? Dr. Harris Coulter, an expert on the pertussis vaccine, co-author of A Shot in the Dark,[130]and author of Vaccination, Social Violence, and Criminality,[131]concludes otherwise.[132] Regarding infectious diseases of the past, he states, "The incidence of all of these infectious diseases was dropping very rapidly, starting in the 1930s. After World War II, the incidence continued to drop as living conditions improved. Clean water, central heating...these are the factors that really affected people's tendencies to come down with infectious diseases much more than vaccines. The vaccines might have added a little bit to that downward curve, but the curve was going down all the time anyway."Dr. Coulter's view is supported by the Australian Nurses Journal: "A careful study of the decline in disease will show that up to 90 percent of the so-called 'killer diseases' had all but disappeared when we introduced immunization on a large scale during the late thirties and early forties."[133] A similar statement is made by the Medical Journal of Australia: "The decline of tetanus as a disease began before the introduction of tetanus toxoid to the general population. The reasons for this decline are the same for the decline in all other infectious diseases: improved hygiene, improved sanitation, better nutrition, healthier living conditions, etc." Alan Phillips elaborates on this theme: "We just assume that vaccinations are responsible for disease decline, which is not the case. For if you check the statistics, you will find that the vast majority of disease decline proceeded vaccines. In the case of measles, for example, there was a 97 percent decline preceding vaccination; in the case of pertussis, 79 percent. When you look at the graph of the decline in death rate over the course of the century, you see that the rate of decline, post-immunization, was virtually the same as the decline preimmunization, suggesting that it's difficult to tell whether or not the vaccine had any effect on an already well-established decline in disease deaths."[134], [135]Phillips attacks the notion that vaccines are responsible for the dramatic reduction in infectious disease during this and past centuries. "According to the British Association for the Advancement of Science, childhood diseases decreased 90 percent between 1850 and 1940, paralleling improved sanitation and hygienic practices, well before mandatory vaccination programs. Infectious disease deaths in the U.S. and England declined steadily by an average of about 80 percent during this century (measles mortality declined over 97 percent) prior to vaccinations. In Great Britain, the polio epidemics peaked in 1950, and had declined 82 percent by the time the vaccine was introduced there in 1956. Thus, at best, vaccinations can be credited with only a small percentage of the overall decline in disease-related deaths this century....[136]Toxic Vaccine Ingredients and Manufacturing Processes. Walene James urges parents to think about the effects the ingredients of vaccines could have on their children's health: "There are three categories of ingredients. The first are cultured bacteria and viruses....The second ingredient in vaccinations is the medium in which they are cultivated. This can include...dog kidney tissue, monkey kidney tissue, chicken or duck egg protein, chick embryo, calf serum, pig or horse blood, and cowpox pus. These foreign proteins are injected directly....They are very toxic since they do not get filtered through the digestive process or pass through the liver.""These proteins are foreign to the body, and are in a state of decomposition. They are composed of animal cells, and therefore contain animal genetic material. It is possible for the genes in these cells to be picked up by the live, attenuated viruses used in vaccines. These viruses then implant a foreign alien genetic material from animal tissue cultures into the human genetic system...."The last category of vaccine ingredients, James says, includes stabilizers, neutralizers, carrying agents, and preservatives. "Many people feed their children healthy foods. They would never think of giving their children formaldehyde...or aluminum phosphate to eat....These are preservatives and carrying agents that are injected...without buffering by the digestive process, or censoring by the liver."[137]As examples of the ingredients used in vaccines, we list the contents of five common childhood vaccines below. These ingredients are current according to the latest information available to us, but they are subject to change at any time:     Hepatitis B vaccine: This genetically engineered, noninfectious viral vaccine is derived from hepatitis B surface antigen produced in yeast cells. The Recombivax HB vaccine (Merck & Co.) uses a fermentation medium consisting of a yeast extract, soy peptone, dextrose, amino acids and mineral salts. The protein is purified, then treated with formaldehyde and coprecipitated with alum (potassium aluminum sulfate) to form bulk vaccine adjuvanted with amorphous aluminum hydroxyphosphate sulfate. There is no detectable yeast DNA in the vaccine, but it may contain not more than 1% yeast protein.[138] For the Engerix-B vaccine (SmithKline Beecham), the antigen is absorbed on aluminum hydroxide, and the product contains no more than 5% yeast protein. The product also contains sodium chloride and phosphate buffers. The pediatric/adolescent and adult formulations of Engerix-B do not have preservatives but may contain a trace amount of thimerosal (a mercury derivative) from the manufacturing process.[139] Recombivax HB is supplied in pediatric/adolescent and adult formulations with and without a preservative.[140]     DPT vaccine: This vaccine includes diphtheria and tetanus toxoids and acellular pertussis vaccine absorbed. The components of the acellular pertussis vaccine are isolated from phase 1 Bordetella pertussis culture grown in a modified Stainer-Scholte medium. They are treated with formaldehyde. For the Tripedia vaccine (Aventis Pasteur), the Corynebacterium diphtheriae cultures are grown in a modified Mueller and Miller medium, while the Clostridium tetani cultures are grown in a peptone-based medium containing a bovine (meat) extract. Both are treated with formaldehyde, and the detoxified materials are purified by serial ammonium sulfate fractionation and diafiltration. The toxoids are absorbed using aluminum potassium sulfate (alum). The product contains sodium chloride, gelatin, and polysorbate 80. The one-dose vial does not have a preservative but contains a trace amount of thimerosal from the manufacturing process; the multidose vial contains thimerosal as a preservative.[141] For the Infanrix vaccine (SmithKline Beecham), the diphtheria toxin is produced in a Linggoud and Fenton medium containing a bovine extract, and the tetanus toxin is produced in a modified Latham medium. Both are treated with formaldehyde, and each is absorbed onto aluminum hydroxide. The product contains 2-phenoxyethanol as a preservative, sodium chloride, and polysorbate 80.[142]     Inactivated polio vaccine: The IPOL product (Aventis Pasteur) is a highly purified, inactivated vaccine that contains three types of poliovirus. The viruses are grown in cultures of VERO cells, a continuous line of monkey kidney cells. The cells are grown in Eagle MEM modified medium, supplemented with newborn calf serum that is tested for adventitious agents before use and originates from countries free of bovine spongiform encephalopathy. For viral growth, the culture medium is M-199, without calf serum. (The residual calf serum protein is less than 1 ppm in the final vaccine.) Neomycin, streptomycin and polymyxin B are used in the production process. The vaccine also contains 2-phenoxyethanol and formaldehyde (0.02% maximum) as preservatives.[143]MMR vaccine: The M-M-R II live virus vaccine (Merck & Co.) contains (1) Attenuvax, a more attenuated line of measles virus propagated in chick embryo cell culture; (2) Mumpsvax, a strain of mumps virus propagated in chick embryo cell culture; and (3) Meruvax II, the Wistar RA 27/3 strain of live attenuated rubella virus propagated in WI-38 human diploid lung fibroblasts. The product contains sorbitol, sodium phosphate, sucrose, sodium chloride, hydrolyzed gelatin, human albumin, fetal bovine serum, and neomycin. It does not contain a preservative.[144]Chickenpox vaccine: The Varivax vaccine (Merck & Co.) is prepared from the Oka/Merck strain of live, attenuated varicella virus. The virus originated from a child with natural varicella. It was introduced into human embryonic lung cell cultures, adapted to and propagated in embryonic guinea pig cell cultures and propagated in human diploid cell cultures (WI-38). The vaccine contains sucrose, hydrolyzed gelatin, sodium chloride, monosodium L-glutamate, sodium phosphate dibasic, potassium phosphate monobasic, potassium chloride, residual components of MRC-5 (human diploid) cells including DNA and protein, and trace amounts of sodium phosphate monobasic, EDTA, neomycin, and fetal bovine serum. There is no preservative.[145]Noting that vaccines include a host of undisputed toxins, such as aluminum phosphate and formaldehyde, Alan Phillips reminds us that many of the ill effects of vaccines did not exist at anywhere near today's levels 30 years ago. He cites autism, ADD, hyperactivity, dyslexia, and a host of allergies as examples.[146]In his book What Every Parent Should Know About Childhood Immunization, Jamie Murphy seconds the views of Phillips: "What could formaldehyde, aluminum, phenol...or any number of other deadly chemical substances used in vaccines possibly have to do with preventing disease in children? The fact that they are needed at all in the vaccine formula argues that the product is toxic, unstable and unreliable with or without their presence."[147]The Use of Thimerosal. In July 1999, the American Academy of Pediatrics (AAP) issued a statement urging the removal of the mercury-containing preservative thimerosal from vaccines.[148] The Centers for Disease Control and Prevention (CDC) reported that as of April 2001, all seven of the vaccines recommended for use in all children contained either no thimerosal or trace amounts only. These vaccines include hepatitis B, Haemophilus influenzae B, and DTaP (which formerly contained thimerosal as a preservative) and MMR, polio, varicella and pneumococcal (which have never contained thimerosal).[149]The FDA explains that the vaccines are now being produced as either thimerosal-free or thimerosal-reduced products. The term thimerosal-reduced, it says, usually indicates that trace amounts of mercury-less than 0.5 micrograms per 0.5 mL vaccine dose-may remain from the use of thimerosal in the manufacturing process, but that thimerosal is not added as a preservative. The term preservativefree means the vaccine does not have a preservative but, again, that trace amounts may remain from the manufacturing process.[150]The reason for the AAP's strong recommendation in 1999 was a growing concern about the risk of exposing the developing brains of infants to mercury. As more vaccines were being mandated for children, the cumulative level of mercury exceeded that deemed safe by guidelines. With the new pediatric vaccines, the FDA says, "the most likely maximum amount of ethyl mercury that an infant may be exposed to from the routine vaccination schedule has been reduced from approximately 187.5 mcg to <3 mcg."[151]While this change is certainly welcomed, we should ask why such a dangerous, known neurotoxin was allowed to be used in vaccines in the first place. Mercury exposure has been associated with nerve cell degeneration,[152] adverse behavioral effects,[153] and impaired brain development.[154] It has also been linked to degenerative chronic conditions such as Alzheimer's disease. The developing fetal nervous system is the most sensitive to its toxic effects, and prenatal exposure to high doses of mercury has been shown to cause mental retardation and cerebral palsy.[155]Yet the CDC recommends the influenza vaccine, which for the most part still contained mercury until late 2002, to all pregnant women, despite the 2001 urging from the Institute of Medicine that "full consideration be given to removing thimerosal from any biological product to which infants, children, and pregnant women are exposed." The CDC's homepage, today, September 6, 2006, quotes, "Today, with the exception of some Influenza (flu) vaccines, none of the vaccines used in the U.S. to protect preschool children against 12 infectious diseases contain thimerosal as a preservative."This means that some of the country's most vulnerable, are still receiving mercury in its shots, as the flu vaccine is recommended for those most at risk, including the elderly, those with weakened immune systems, and very young children.In 2001 the FDA was in discussions with manufacturers of influenza virus vaccines regarding the development of thimerosal-free or -reduced products.[156]According to the CDC, one manufacturer of influenza vaccine, Evans Vaccines, had reduced-thimerosal influenza vaccines available by the 2002-2003 flu season. This Fluvirin product had less than 1 mcg of thimerosal per dose; other influenza vaccines at the time had 25 mcg.[157] For the pediatric market, another manufacturer, Aventis Pasteur, announced in September 2002 that the FDA had approved a license to market a preservative-free influenza vaccine for infants aged six to 35 months. A supply of the preservative-free Fluzone was available for the 2002-2003 flu season.[158]Despite the change over, this still begs the question as to how many children are still suffering the effects of mercury-toxic injections from as late as the 2000 and 2001 flu seasons.It should also be noted that while the mercury content of childhood vaccines has been eliminated or greatly reduced, vaccines may still contain formaldehyde (a highly carcinogenic material used to embalm corpses) and/or aluminum.New vaccines continue to be approved:  in 2003 the "first live attenuated influenza vaccine licenced for 5-49 year old persons"[159] was approved, and in 2004 "inactivated influenza vaccine was recommended for all children 6-23 months of age"[160]However, the CDC site does not state specifically which flu vaccinations contain the thimerosol: "certain Influenza (flu) vaccines and tetanusdiphtheria vaccines (Td) given to children age 7 and older contain thimerosal as a preservative."Unproven Vaccines, Unmonitored Medicine The widespread use of experimental vaccines during Desert Storm has often been cited as a possible cause of Gulf War syndrome. Dr. Garth Nicolson elaborates: "I'm not a big fan of experimental vaccines. There have been too many mistakes. Usually you find these things out years later. Often agents that we think innocuous turn out to be harmful." He explains that during the Gulf War, the established procedures of vaccination were ignored. Normally, only one inoculation should be given at a time, but the military insisted on giving multiple shots at once, which, according to Nicolson, is the worst thing you can do because it suppresses the immune system. [5]The troops immunized for the Gulf have been called guinea pigs, and for good reason. They received experimental vaccines, e.g., those for anthrax and botulinum that were not approved for use by the FDA and have since proven to cause potentially dangerous side effects. In 1991,  "Anthrax vaccine was administered to about 150,000 troops in the [Gulf War] theater, about 1/5 of those deployed."[161] Soldiers who were given these experimental vaccines, without informed consent, have reported suffering from a variety of neurological problems and aberrant bleeding from all parts of their bodies. Because of these vaccines' experimental nature, many questions have arisen as to why our government dispensed them. Not the least of these questions is, what about the Nuremberg Code? Developed by the Allies after World War II in response to inhumane Nazi experimentation, the Nuremberg code says that voluntary and informed consent is absolutely essential from all human subjects who participate in research, whether during peace or war. [11]Vaccine Failures. According to Phillips, "The medical literature has a surprising number of studies documenting vaccine failure. Measles, mumps, smallpox, and polio outbreaks have all occurred in vaccinated populations. In 1989, the CDC reported: Among school-aged children, [measles] outbreaks have occurred in schools with vaccination levels of greater than 98 percent. They have occurred in all parts of the country, including areas that had not reported measles for years. The CDC even reported a measles outbreak in a documented 100 percentvaccinated population. A study examining this phenomenon concluded, 'The apparent paradox is that as measles immunization rates rise to high levels in a population, measles becomes a disease of immunized persons.'...These studies suggest that the goal of complete immunization is actually counterproductive, a notion underscored by instances in which epidemics followed complete immunization of entire countries....In the U.S. in 1986, 90 percent of 1,300 pertussis cases in Kansas were 'adequately vaccinated.' Seventy-two percent of pertussis cases in the 1993 Chicago outbreak were fully up to date with their vaccinations."[162], [163], [164], [165], [166], [167], [168], [169], [170]Effects of Specific VaccinesWith this section, we begin an examination of the effects of specific vaccines. Seven vaccines will be covered in this and the next two installments of this series: diphtheria, pertussis and tetanus, polio, chickenpox, hepatitis B, measles, mumps and rubella, smallpox, and the now-withdrawn rotavirus vaccine.DIPHTHERIA, PERTUSSIS, AND TETANUS VACCINESDiphtheria VaccineIn the 15 years following the introduction of the diphtheria vaccine in 1894, the number of deaths in England and Wales rose 20 percent. Between 1895 and 1907, there were 63,249 cases of diphtheria in individuals treated with anti-toxin; 8,917 people died, a fatality rate of 14 percent. In the same time period, there were 11,716 cases not treated with anti-toxin; only 703 died, a fatality rate of 6 percent.From a book by Greg Beattie, entitled, "Vaccination A Parent's Dilemma," we examine official charts taken from the Commonwealth of Australia, on the decline in death rates from Whooping Cough, Diptheria, measles, and Scarlet Fever.  We see that in each case, the bulk of the death rates from each illness declined in large measure even before the vaccine for the illness had been given.  Lest we think, however, that these may be figures unique to Australia, the author states that, "Graphical evidence on the decline in death rates from infectious disease for USA, England, New Zealand and many other countries shows the exact same scenario[s]"  Whooping cough death rates, for example, when the vaccinations were given, between 1940 and 1960, had already declined to almost a tenth of their original rate at their height in 1880.  During the decade between 1940 and 1950, when the Diptheria vaccine was originally given, death rates had declined to almost a quarter of their rate in 1880, and the measles deaths, at their height in the 1900's, had already declined to its modern low rates by the mid 1960's, when the first vaccine was given.  The CDC's paper on reduction of illnesses in the 20th century mentions that one of illnesses that was reduced to zero by the year 2004, was diptheria, from an average of 21, 053 deaths per year in the 20th century.We know from Greg Beattie's work that the earliest vaccinations for childhood illnesses were given in the late 1930's for diptheria.  When we  examine the figures from the Union soldiers'study, mentioned earlier; we note that only the last of the children for the later cohort (1918-1927) would have been children when the Diptheria vaccinations were given.   Although heart damage can occur in untreated Diptheria cases, most Diptheria onset occurs in adolescents and adults.  Most of the later cohort would already have been adolescents at the time of the Diptheria vaccine, so it is unlikely that the onset of the Diptheria vaccination alone had an effect on the outcome of delayed onset of heart disease already noted in this group of people. 47 48 49 50Similarly, it may be true that childhood illnesses could have a role in the formation of joint inflammation later in life, but again, only the last children of the later cohort in the union soldiers' study would have received the Diptheria vaccine in later childhood, so this would have a negligible effect on the outcome of all joint pain in this cohort group.  Acellular Pertussis VaccineUntil 1996 the whole-cell vaccine was the only whooping cough vaccine available in the U.S. for children in their first year of life. This vaccine included all the components of the bacterium Bordetella pertussis, including the toxic ones, and was associated with high rates of adverse reactions. In Japan, a lack of trust among the public of the whole-cell vaccine led to the development of a new, purified acellular vaccine that has been used exclusively in the country since 1981.[171]Even though a safer vaccine was widely used in Europe and Japan, it wasn't until 15 years later that the purified acellular pertussis vaccine was approved by the U.S. FDA for use in combination with the diphtheria and tetanus toxoids for all doses in the vaccination series.[172] A 1996 study showed that the rate of adverse reactions reported to VAERS in 1991 to 1993 dropped from 9.8 per 100,000 vaccine doses to 2.9 per 100,000 after substitution of the acellular pertussis vaccine for the whole-cell vaccine for the fourth and fifth dose of DPT vaccination.[173]Vaccine Failure. Ninety-one percent of pertussis cases in Nova Scotia, Canada, had received at least three doses of vaccine. Researchers concluded that "pertussis remains a significant health problem in Nova Scotia despite nearly universal vaccination."[174] In this case, the pertussis vaccination proved ineffective.Pertussis vaccination also has been shown to increase the susceptibility of certain individuals to the infection, as a 1997 report by the CDC clearly describes. In the Netherlands, 96 percent of children have received at least three shots of pertussis vaccine by the age of 12 months. Yet pertussis has been endemic in the country for the past two decades.[175]Increasing Cases of Pertussis in Infants and Adults. After the United States mandated pertussis vaccination in 1978, the incidence of the disease in the following eight years trebled. While cases of pertussis were increasingly seen among every age group, the highest incidence was registered in infants less than 1 year old, and the highest relative increase was seen in adolescents and adults. It is important to note that infants suffered from the most complications, with rates of hospitalization, pneumonia, convulsions, and encephalopathy being the highest in children 0 to 6 months old.[176]According to one article, the incidence of pertussis increased each year in England and Wales after an accelerated immunization schedule was introduced.[177]Since the immunity provided by the vaccine, unlike that derived from natural infection, is only temporary, more adults are now contracting the disease and are transmitting it to infants, where the infection manifests with particular severity and can often lead to death.Epidemics of pertussis striking infants have also been reported in Australia, despite extensive vaccination coverage.[178]DPT Safety. The U.S. Department of Health and Human Services estimates that every year approximately half a million DPT shots are followed by reactions severe enough to contraindicate the administration of more pertussis vaccine. One in seven children should be turned away for further pertussis vaccine. In practice, though, this does not happen. [179], [180] And, as pointed out by Alan Phillips, "The FDA's VAERS (Vaccine Adverse Effects Reporting System) receives about 11,000 reports of serious adverse reactions to vaccination annually, some 1 percent (112+) of which are deaths from vaccine reactions. The majority of these deaths are attributed to the pertussis (whooping cough) vaccine, the 'P' in DPT. This figure alone is alarming, yet it is only the tip of the iceberg. The FDA estimates that only about 10 percent of adverse reactions are reported...."DPT Vaccination and Neurological Damage. The scientific literature contains documentation of the damaging effects of DPT vaccination on the nervous system. Neurological complications include convulsions, hypotonichyporesponsive episodes (a collapse-shock-like status), paralysis, and encephalopathy.FURTHER READINGS: Articles in the literature associate DPT vaccinations with neurological problems[181], [182]and convulsions.[183], [184], [185], [186]DPT Vaccination and Asthma. In a 1994 study published in the Journal of the American Medical Association, Dr. Michel Odent found that children immunized against whooping cough were five times more likely to suffer from asthma than those who did not receive the vaccine.[187]Dr. Odent's is not a solitary voice. Another study, performed by Farooqi et al. on almost 2,000 children born between 1974 and 1984, showed that vaccination against whooping cough is associated with a 76 percent increased risk of developing asthma and other allergic diseases later in life.[188]     DPT Vaccination and SIDS. Sudden infant death syndrome (SIDS) is the unexpected death of a child occurring without any apparent explanation, and for which autopsy cannot reveal a determining cause. Every year, 5,000 to 6,000 children die from SIDS. The incidence peaks in infants aged 2-4 months, which correlates with the introduction of a majority of vaccine injections. It is worth noting that approximately 85 percent of SIDS cases occur during the first six months of life, and that the first three DPT shots were given to children at 2, 4, and 6 months of age when these studies were conducted.A study conducted by researchers at the Mayo Clinic looked at the incidence of SIDS in Olmsted County, Minnesota, over several decades and found that it increased steadily from a rate of 0.55 per 1,000 live births in 1953 to 128 in 1992. That's a great increase in this 40-year study period. However, when the authors compared mortality from SIDS to overall infant mortality, they came up with an even more distressing finding. The increase of SIDS as a percentage of total infant deaths increased from 2.5 in 1953 to 17.9 in 1992.[189] So from 1950 to 1990, a combination of lifestyle changes, improved sanitary conditions, and progress in medical technology resulted in a reduction of practically all causes of infant death except one-sudden infant death.In 1982, at the 34th Annual Meeting of the American Academy of Pediatrics, Dr. W. Torch presented an abstract entitled "Diphtheria-PertussisTetanus (DPT) Immunization: A Potential Cause of the Sudden Infant Death Syndrome (SIDS)." Triggered by a report of 12 such deaths occurring within 3-1/2 to 19 hours of DPT vaccination, Torch's investigation looked at 70 SIDS cases. He found that two-thirds of the victims had been vaccinated from a half day to three weeks prior to death.[190]Torch reaffirmed a link between DPT and SIDS in 1986, when he presented 11 new cases of SIDS and one of near-miss syndrome (NMS) occurring within 24 hours of DPT injection. All cases presented with SIDS pathology, yet none were diagnosed as "postvaccinal" death.[191] Analysis of these and other more than 150 cases of DPT postvaccinal deaths reported in the literature-about half of which were sudden or anaphylactic-led Torch to conclude that "Although many feel that the DPT-SIDS relationship is temporal, this author and others maintain a casual relationship exists in a yet-to-be-determined SIDS fraction."[192] Other researchers also have uncovered a relationship between DTP immunization and SIDS.[193], [194]Tetanus Vaccination and Neurological Damage. The literature includes articles on neurological reactions to the tetanus vaccination[195], [196], [197], [198], [199], [200] and other adverse reactions.[201], [202], [203]In Part 2: The effects of vaccines for polio, chickenpox, hepatitis B, and measles, mumps and rubella.Vaccination: Pain, Profit, and Politics - Part 2By Gary Null, Ph.D., and Martin Feldman, M.D.In Part 1 of this series, we discussed the reasons why we should challenge our assumptions that vaccines are safe and effective. These reasons include the adverse effects associated with vaccines, the unsound principles on which they are based, questions about whether immunization really eliminates disease, the toxic ingredients used in vaccines, and vaccine failures. In Part 1 we also began to look at the effects of specific vaccines with a discussion of the diphtheria, pertussis and tetanus vaccine; we continue that process in Part 2 with a look at the polio, chickenpox, hepatitis B, and measles, mumps and rubella vaccines.Polio VaccineThree types of polio vaccines have been used throughout the world: 1) the OPV, or oral polio vaccine (Sabin vaccine), consisting of live, attenuated poliovirus; 2) the IPV, or inactivated polio vaccine (Salk vaccine), consisting of killed poliovirus and given by injection; and 3) the eIPV, an enhanced potency inactivated polio vaccine, consisting of killed poliovirus with high viral antigen content.Today, the Advisory Committee on Immunization Practices (ACIP) recommends exclusive use of the IPV for routine childhood polio vaccination in the U.S. (the enhanced-potency version is the only IPV in use in the U.S.). The ACIP changed its polio vaccine recommendation to the all-IPV schedule, effective January 2000, to eliminate the risk for vaccine-associated paralytic poliomyelitis (VAPP), the condition caused by the previously recommended oral polio vaccine.[204]Until 1996, all children in the U.S., except those with a compromised immune system and their close contacts, were immunized with the live attenuated OPV vaccine. However, the vaccine actually caused polio in a small percentage of people. According to the CDC, the overall risk for VAPP is approximately one case in 2.4 million OPV doses distributed, while the first-dose risk is one case in 750,000 doses distributed. In fact, the only indigenous cases of polio reported in the U.S. since 1979 have been associated with the use of OPV. Between 1980 and 1998, 144 cases of VAPP were reported.[205]Despite these occurrences, the ACIP recommended the use of OPV in the U.S. because it believed the benefits of the oral vaccine outweighed the risk for VAPP. In 1996, the ACIP recommended a sequential schedule of IPV and OPV to "decrease the risk for VAPP but maintain the benefits of OPV." It then recommended the allIPV schedule as of January 2000, citing several reasons: the substantially reduced likelihood of poliovirus being imported into the U.S. due to rapid progress made in the global polio eradication initiative; the acceptance of the sequential schedule; and the lack of declines in childhood immunization coverage.[206]The CDC states that, "in 1955 the inactivated polio vaccination was licenced."[207]  In 1954, the largest vaccination trial to date was undertaken across the country.  Up to 600,000 children throughout the country were vaccinated due to efforts by parents, community activists, and teachers, both in the efforts of pursuing science and bettering public health.  Children and their parents were told that they were 'pioneers' in an effort to eradicate a debilitating scourge.  In homage to the passionate public effort, researchers stated that 95% of children received the three shots required by the trial.    Whereas the design of the study was vigorous, there were complaints as to the follow through. The setup of the study was as follows: Each child received three vaccinations on a rigorous schedule, and the two arms of the study had differing control groups which would even out the counterbalancing effects of income, nutrition, and class; however, it was often reported that the entire dose was not given per child, or that in the control group which was to have received a placebo injection, liquid from the experimental group remained in the syringe, thereby giving the placebo child a weak inoculation.  Despite the fact that the government review of the outcome of polio vaccination was to have been considered positive, critics said that there was not a huge difference between the observed and placebo control groups and the actual groups that received the vaccinations.In three of the trial groups, numbers of children in the study tested were between 200,000 and 225,000.  In order to compare effectiveness, we will average the outcomes based on numbers tested at 200,000:Therefore, for in areas where a placebo shot was given, along with the vaccination, an average of 32.87 children came down with polio out of 200,000 who received the shots, whereas an average of 114.30 children out of 200,000 came down with the illness who did not receive the vaccination.  In the next cohort group, an average of 34.24 children out of 200,000 came down with polio after receiving the vaccination whereas an average of 91.01 children out of 200,000 came down with polio in the control group who was just observed rather than actually receiving the shots.  Although the numbers for the two arms of the study may be similar, it appears that the lower number in the observational control may be slightly more accurate for a couple of reasons:  First, there were complaints that the actual givers of the vaccines contaminated the control groups with the active vaccine, and second, the control group of observed children was much larger than the control group who received a placebo [725, 123 as compared to 201, 229 in the placebo group];  it is well known that a larger cohort group is desired for better scientific accuracy.The one positive aspect of the placebo arm of the study as noted by author David Oshinsky was that the children were more likely to be of the same age, class, and upbringing, since those who were vaccinated tended to have parents who were better educated and more willing to commit their children to a scientific study for the 'betterment of scientific inquiry'.  It is just such attitudes that we wish to examine closely in this paper, for these are the vulnerabilities that the mainstream medical community uses when coercing the public to use vaccinations.[208]After the auspicious start as seen by the CDC's National Immunization program, we will examine the timeline for the various vaccinations given in the US:Polio was seen originally as a mystery because the sanitation measures that had brought typhoid and cholera into abeyance did not seem to have an effect on polio.  In fact children brought up in middle class homes were more likely to develop the paralyzing illness than those in poorer neighborhoods.  For example: "[Franklin Roosevelt] had avoided the common illnesses until his arrival at boarding school as a teen.  From that point forward, his medical history resembled an encyclopedia of contagious diseases.  The list included typhoid fever, swollen sinuses, infected tonsils, stomach problems, endless sore throats."[209]  We know that later he was said to have contracted polio but some have attributed his illness to Guillain Barre syndrome as well, which we see below, has an association with Polio.Originally, The Polio outbreaks were one of the first times it was suggested that a less-antiseptic environment may have had a protective effect upon the child.  It was later found that polio was a viral infection, and was passed through the mouth,[210]but was an infection of the digestive tract that spread through the nerves to the brain and spinal cord.  One of the early researchers on polio noticed that boys tended to get polio more often than girls, and during periods where they had stressed their bodies, such as playing outside on a hot day.  Franklin Roosevelt was said to have contracted polio after playing rigorously in the water with his children.  Whether rich or poor, however, author David Oshinsky points not to large issues of public sanitation, but to issues of personal hygiene: "the words 'American' and 'cleanliness' rarely graced the same sentence before the twentieth century.  In 1900 toothbrushes were still rare in the United States, deodorants and shampoos almost unheard of.  Few people bathed more than once a week or rinsed their hair more than once a month.  Fewer still washed their hands before eating or after using the toilet.  Spitting was almost universal.  Travelers shared beds and chamber pots with complete strangers.  Most houses, lacking screens, attracted swarms of insects in warm weather.  Water supplies were unfiltered, and food was poorly refrigerated, if at all."[211]It is clear to anyone with a modicum of common sense that these would be ideal conditions to spread a virus of the digestive tract.  In an article entitled Introduction to Contagion[212], we discover that it is important to note the way a disease is transmitted when examining the ways in which the epidemics have happened throughout the ages:For example: whether virus or bacteria, there are illnesses that are spread through droplets that are ingested, which are present in the air due to respiratory expulsion.  There are also water borne illnesses, that can be picked up by a cut in the skin or when a person ingests quantities of water from an infected source.  Other diseases can be transmitted through food, and still others through physical touching, such as through the hands, through the saliva, or through sexual contact.In an epidemic of cholera, for example, the CDC states that,"the source of the contamination is usually the feces of an infected person. The disease can spread rapidly in areas with inadequate treatment of sewage and drinking water."[213]David Oshinsky writes of non-polio outbreaks:  "mortality rates had dropped dramatically since the 1870's, the result of better sanitation, a healthier diet, and stunning breakthroughs in research...Other epidemic diseases like cholera and typhoid fever had been tamed by better sanitation, attacking the filth that spread their deadly germs.  In most places this involved the regulation of sewage, the purification of water, and the pasteurization of milk.  It included public health campaigns to educate people about quarantining the sick and keeping their dwellings clean."[214]Guillain-Barre Syndrome and Polio Vaccine. Guillain-Barre syndrome (GBS) is a disease that involves the nervous system and is characterized by muscle weakness, numbness, loss of reflexes, and paralysis. In Finland in 1985 there was an increase in the incidence of Guillain-Barre syndrome that followed by a few weeks the implementation of a nationwide oral poliovirus vaccine campaign.[215], [216] And in Brazil, analysis of 38 cases of paralysis diagnosed as GBS led in all cases to the isolation of the vaccine strains of the poliovirus. All patients had been vaccinated with the oral polio vaccine months or years before the onset of symptoms.[217]Furthermore, vaccine viruses also have been isolated from patients with paralysis diagnosed as transverse myelitis (TM), and in patients with facial paralysis (FP).[218] Most individuals with TM and FP had received the oral polio vaccine months or years prior to the onset of disease, indicating that the virus may remain latent and revert to virulence later in time. It is noteworthy too that in Brazil, cases of wild-type poliomyelitis have not been reported since 1989, while vaccineassociated paralysis is still occurring.[219]The Cancer Connection to the Polio Vaccine. In 1960 it was discovered that both the Salk and Sabin vaccines, which had been administered to millions of people, were contaminated with SV40 (simian virus 40), derived from the monkey kidney cells used to grow the vaccine viruses. The SV40 survived inactivation with formaldehyde, the method used to kill the poliovirus, and was therefore injected with the vaccine into 98 million people in the U.S.[220] and hundreds of millions worldwide. These individuals today have SV40 sequences integrated into their genetic code. Animal studies have demonstrated the ability of SV40 to integrate its DNA into that of the host cell and to induce malignancy. Unfortunately, a growing number of studies are showing that the virus retains these same properties in humans as well as in animals. Integration and replication of SV40 has been documented in 13 percent of non-Hodgkin's lymphomas,[221] 16 percent of Hodgkin's lymphomas,[222] 11 percent to 90 percent of different types of brain tumors,[223],[224],[225],[226] 83 percent of mesotheliomas (malignant tumors of the lining of the lungs),[227] 28 percent of bronchopulmonary carcinomas,[228] 50 percent of osteosarcomas,[229] and more than 33 percent of other types of bone tumors.[230],  [231]Chickenpox VaccineIn 1995 the American Academy of Pediatrics (AAP) and the ACIP recommended universal chickenpox (varicella) vaccination of children aged 12 to 18 months. They also recommended that the vaccine be given to children aged 18 months to 12 years who have not been vaccinated or who lack a reliable history of the disease.The fact is that in the vast majority of cases, chickenpox is a benign, selflimiting disease in children. Natural immunity, derived from contracting the disease, is permanent. Vaccine-induced immunity, on the other hand, is only temporary, lasting an estimated six to 10 years. The temporary nature of vaccine-induced immunity can create a more dangerous situation by postponing the child's vulnerability until adulthood, when death from the disease is 30 times more likely.The National Vaccine Information Center (NVIC), Vienna, Va., advises parents to seriously consider not using the chickenpox vaccine on healthy children. Barbara Loe Fisher, cofounder and president of the NVIC, elaborates: "Our organization is questioning the recommendation...that all healthy children be vaccinated with the chickenpox vaccine...."...In children, chickenpox is, by and large, a very mild disease. The case/fatality ratio in healthy children is 1 death per 100,000 children. In adults it rises to 31 deaths per 100,000. So it basically is an experiment. That is really what happens with most of these vaccines that they bring out. They really don't know what the long-term effect is going to be. "The other thing about the chickenpox vaccine is that the vaccine virus could lie dormant in vaccinated individuals, and then reactivate later in life in the form of herpes zoster, which is also known as shingles, or perhaps [in the form of] other immune system disorders...." Fisher is not the only one to question the appropriateness of the official recommendations concerning this vaccination. According to the results of one survey, 58 percent of pediatricians interviewed did not recommend varicella vaccination of all infants.[232]Discounting the numerous concerns of doctors, researchers, and parents, in February 1999 the CDC expanded its guidelines for varicella vaccination and required that all children entering child care centers and elementary and middle schools receive varicella vaccination unless they have evidence of immunity.[233]In the meantime, 6,580 adverse events-including 14 deaths-were reported to the Vaccine Adverse Events Reporting System in association with varicella vaccination between March 17, 1995 and July 25, 1998.[234] The actual number could be at least 10 times higher, if we take into consideration the proven fact that only 10 percent of adverse events are commonly reported.Another concern regards pregnant women. Normally, 90 percent of adult women are immune to varicella and transfer this immunity to their babies during pregnancy. But the immunity induced by vaccination, which lasts only five to 10 years, may be gone by the time a woman enters her reproductive stage, leaving pregnant women at risk of contracting the infection and transmitting it to the fetus. Fetal varicella syndrome is characterized by multiple congenital malformations and is often fatal for the fetus.[235] Thus, we need lifelong immunity from natural infection.In addition, children born from women whose vaccine-induced immunity has faded are unprotected during their first year of life, when their immune system is still developing, and may suffer fatal complications should they be exposed to the infection.Is the Chickenpox Vaccine Effective? If the effectiveness of the vaccine is measured by its ability to prevent the disease from occurring, the answer is simply no. As we read in an article published in Pediatrics, "In 1998, three years after vaccine licensure, child care centers in Los Angeles County continued to report varicella outbreaks." These outbreaks occurred in child care centers with high vaccine coverage as well as in those with low coverage, meaning that the infection spread regardless of child vaccination status.[236]An interesting article clearly shows how questionable the data are claiming reductions of diseases following immunization campaigns. This is what often happens: Reporting of a specific disease is encouraged until the start of a vaccination program. Thus, the disease appears to be present at certain rates. Then, after the vaccine enters the market, reporting is no longer required and therefore not done, and the rates of the disease seem to drop. But in reality the drop results from changes in reporting requirements and practices, not from an actual decline in the number of cases.Vaccination against chickenpox will not prevent a child from contracting the disease. Rates of infection in vaccinated individuals-so-called "breakthrough varicella"-range from 18 percent to 34 percent in the 10 years following immunization.[237], [238], [239] Furthermore, even if vaccination reduces the number of skin lesions, the duration of the infection, and the occurrence of fever in individuals who develop breakthrough disease, it does not reduce the rate of constitutional complaints and that of complications.[240]One study found that 18.6 percent of children who responded to varicella vaccination developed breakthrough disease after exposure to the infection in the five to 10 years following immunization.[241] Another study showed that 20-30 percent of vaccinees developed varicella in the 10 years following immunization.[242]In a third study, 34 percent of individuals vaccinated against chickenpox developed breakthrough disease in the seven to 10 years following immunization.[243]FURTHER READINGS: Articles discuss the potential downside to the mass use of the chickenpox vaccine and reactions associated with it.[244], [245],  [246]Hepatitis B VaccineThe hepatitis B vaccine, commercially available in the United States since 1982, was supposed to be given to every American child within 12 hours of birth. In spite of this measure, "the incidence of acute hepatitis B in this country has risen from 55 per 100,000 in 1981 to 63 per 100,000 in 1987," according to the New England Journal of Medicine.[247]          Additionally, strong side effects have been reported following the use of this vaccine. In 1990, the Journal of Pediatric Child Health had this to say on the subject: "There have...been reported six serious illnesses in a series of 200,000 hepatitis vaccinations, including aseptic meningitis, grand mal seizure, and possible transverse myelitis, as well as 56 minor illnesses considered likely due to the vaccine. These minor illnesses include neurological tremors, Bell's palsy, hives, herpes zoster, psoriasis, musculoskeletal generalized myalgia, joint inflammation...influenza-like syndrome, injection site reaction, diarrhea, vomiting, and headache." The authors conclude with these recommendations: "Until further evidence can be gathered on possible side-effects or complications from the hepatitis B vaccine, it may be worth considering only giving the vaccine to people at high risk, rather than to all the population." According to Barbara Loe Fisher, "Today, hepatitis B recombinant vaccine used in the U.S. is derived from hepatitis B surface antigens produced in yeast cells. A portion of the hepatitis B virus gene is cloned into the yeast (a common baker's yeast) and the vaccine is produced from cultures of this recombinant yeast strain. The vaccine is treated with formaldehyde and contains...hepatitis B virus surface antigen...yeast protein [and] aluminum hydroxide...."[248]The unfortunate reality is that vaccination against hepatitis B has played an uncertain role in preventing the spread of the infection in high-risk individuals. In fact, the incidence of hepatitis B infection has risen 37 percent since the introduction of the vaccine.[249] Despite the evidence of vaccine failure, though, in 1991 the CDC recommended universal hepatitis B immunization of infants.[250]Though substantial decrease in deaths were shown for various illnesses throughout the 20th century, many illnesses still show a significant number of deaths, which calls to question what is really causing the decreases in deaths from particular illnesses:  For example, Hepatitis A was reduced from 117,333 average deaths in the 20th century to 24, 291 in 2004.  Similarly, Hepatitis B went from 66, 232 per year during the entire 20th century to 17358 in 2004.  What is misleading about the chart is that we do not know how many people throughout the 20th century had been vaccinated against hepatitis before they died, or that the apparent greater than 70% decrease in deaths for both Hep A and Hep B were due to vaccination or other health factors.  It is also known that Hep B infection when untreated can cause liver cancer, so we may not know the final outcomes for some Hep B related mortality for those who were infected in the year 2004, for some time yet.Health care workers have not rushed to get this injection. A 1990 article in the British Medical Journal reports that 86 percent of 598 doctors questioned about hepatitis B vaccine believed all general practitioners should receive it, but 309 of these doctors had not been vaccinated themselves.[251] In another study, only 25 percent of nurses and 49 percent of doctors had been immunized, despite the fact that 87 percent of the medical staff and 57 percent of the nurses reported a history of needle stick injury.[252] And the reaction among family physicians is even less enthusiastic: Only 17 percent of 300 family physicians agreed that a recommendation of hepatitis B vaccination was warranted for all newborns in their practice.[253]Is the Hepatitis B Vaccine Safe? As we learn from a study published in thePediatric Infectious Diseases Journal, between 1991 and 1994, 12,520 adverse reactions to hepatitis B vaccination were reported to the Vaccine Adverse Event Reporting System, with 14 percent of these reactions involving newborns and infants.[254]The fact is that the number of reports of complications following hepatitis B vaccination is growing steadily. The Association of American Physicians and Surgeons (AAPS) reports, "About one-third of the reactions were serious enough to result in an emergency room visit or hospitalization, and there were 440 deaths, including about 180 attributed to sudden infant death syndrome or SIDS."[255]The purpose of vaccinations is to reduce the risks of complications associated with the diseases they are designed to prevent. Complications from a vaccine should not outweigh those derived from the disease. And yet, according to Dr. Philip Incao, who has studied vaccinations and the immune system for three decades, in the case of hepatitis B, "...the conclusion is obvious that the risks of hepatitis B vaccination far outweigh its benefits."[256]Dr. Jane M. Orient, executive director of the Association of American Physicians and Surgeons, puts the facts plainly. According to a recent federal government study, she says, "children younger than 14 are three times more likely to die or suffer adverse reactions after receiving hepatitis B vaccines than to catch the disease."[257]Is the Hepatitis B Vaccine Effective? Vaccine supporters claim that the development of an antibody response to the virus contained in the vaccine equals protection against the disease. So we are now vaccinating millions of children against hepatitis B to prevent them from contracting the disease later in life. But for this to happen, the level of antibodies that are supposed to be protective has to remain high for very long periods. The evidence proves that this is not happening.A study published in the New England Journal of Medicine evaluated the persistence of anti-hepatitis-B antibodies in 773 homosexual men immunized against the virus. Of these, 635 produced antibodies. After five years, however, such antibodies no longer existed in 15 percent of the respondents, and their levels declined sharply-below levels deemed to be protective-in another 27 percent. In fact, hepatitis B developed in 55 men, and two individuals became carriers of the hepatitis B virus.[258] Another study shows that after three years, 36 percent of individuals who initially responded to the hepatitis B immunization lost anti-heptatitis-B antibodies.[259]Why then are we needlessly vaccinating millions of children if by the time they'll be adults and might be exposed to the virus, they won't have the antibodies that are supposed to protect them? And, in any case, are these antibodies offering protection against the disease?          Adverse Reactions to Hepatitis B Vaccine. The National Vaccine Information Center, in its report on hepatitis B vaccination, cites 38 reports in the international medical literature presenting evidence that hepatitis B vaccination is causing chronic autoimmune and neurological disease in children and adults. Yet this is not information given in the vaccine manufacturer's literature.Tourbah et al. reported in a 1999 article published in the journal Neurology that eight patients developed encephalitis and central nervous system demyelinating disease within 10 weeks of receiving hepatitis B vaccination.[260]          FURTHER READINGS: Articles in the medical literature associate the hepatitis B vaccine with complications affecting the nervous system[261], [262], [263], [264]and the joints[265], [266], [267], [268], [269] as well as other adverse effects.[270]Measles/Mumps/Rubella (MMR)VaccineAs with hepatitis B, physicians are notoriously reluctant to follow their own advice when it comes to measles vaccination. One study reported that obstetrician gynecologists had the lowest vaccination rate among doctors for the German measles vaccine. Pediatricians didn't fare much better. The authors attributed such findings to "fear of unforeseen vaccine reactions."[271]The fact that the MMR vaccine is particularly ineffective, with a high percentage of those inoculated getting the disease, is undoubtedly a factor here.[272], [273], [274], [275], [276], [277], [278], [279], [280], [281], [282], [283]According to The New England Journal of Medicine, 60 percent of all measles cases among American schoolchildren between 1985 and 1986 occurred in those who were vaccinated.[284]  Scientist Trevor Gunn also points out that for several reasons, there is underreporting of illness caused by vaccination.  These include:  financial backlash from vaccination producers, and the restricted length of time for which adverse symptoms must occur-In England "72 hours for whooping cough and 8-20 hours for the MMRP" vaccines.The Journal of the American Medical Association published a study indicating that among 235 cases of student measles reported in Dane County, Wisconsin, in 1986, more than 96 percent had received a measles vaccine.[285]A study reported in Morbidity and Mortality Weekly found that 58 percent of 1,600 cases of measles in Quebec, Canada, in 1989 occurred in those who had already been vaccinated.[286]And the World Health Organization has conceded that those administered the measles vaccine have a 14 times greater likelihood of contracting the disease than those who remain unvaccinated.[287]Jamie Murphy, author of What Every Parent Should Know About Childhood Immunization, believes that the vaccine may in fact be causing the illness. "In one Chicago study," he says, "90 percent of people vaccinated for measles got measles. Another group did not get vaccinated and had a very low percentage of measles." Murphy believes that this information should serve as a red flag, causing people to realize that vaccines are not working.[288]Murphy's observation raises a question that no one has answered: Why are people who are vaccinated for these conditions getting them? He thinks the answer is that the vaccine does not provide true immunization."The vaccine can never duplicate the kind of immunity that we get from nature. Back in the 1950s, when I got the measles and 80 percent of children got either measles or mumps...it strengthened your immune system....Also, when a natural epidemic of measles occurs, as it does every three to four years in the United States, those children who have been vaccinated, because they did not get a true immunity from the vaccine, become susceptible to measles."The CDC states that there has been a resurgence of measles in the United states in the past few years, but attributes the problem to the rise in un-vaccinated children.Murphy argues that rather than preventing measles, the vaccine may simply be suppressing it, only to have it manifest as other forms of disease with age.[289] He asserts that quite a few diseases are associated with the measles vaccine, including "encephalopathies (brain damage), aseptic meningitis, cranial nerve palsy, learning disabilities, hyperkinesis and severe mental retardation...."[290]          Results of two separate studies by the Institute of Medicine, one in 1991 and another in 1994, showed there to be strong evidence that the MMR vaccine can cause acute arthritis, anaphylaxis, thrombocytopenia, and even death.[291]Even the package insert accompanying the MMR vaccine says that the vaccine may lead to arthritis or arthralgia, either long-term or temporary.[292] Meryl Dorey, editor of the Australian publication Vaccination? The Choice is Yours and president of the Australian Vaccination Network, points out that the MMR vaccine is also associated with Guillain-Barre paralysis, multiple sclerosis, and aseptic meningitis, a swelling of the lining of the brain, which can be fatal. "According to Japanese studies," she notes, "one in 1,044 children who get this vaccine can get aseptic meningitis. It's one of the reasons why Japan withdrew the use of the MMR vaccine in 1994."[293]Viera Scheibner, a retired research scientist, reports that "In April 1993, the Ministry of Health and Welfare in Japan decided to discontinue the use of measles, mumps, and rubella vaccine (Sawada et al., 1993). This decision was prompted by published reports of vaccinated children and their (unvaccinated) contacts contracting mumps from the MMR vaccine, and reports of one in 1,044 vaccinees developing encephalitis."[294], [295]Dorey highlights the problem of shed vaccine virus, noting that it is incorrect to say that the MMR vaccine viruses are not infectious. "According to a study published in the British Medical Journal, July 4, 1987, immunocompromised children should be kept away from MMR vaccinated children for two weeks after vaccination due to the...[possible shedding] of the virus."These events of infection occur because the vaccines contain live virus which can grow in the body and are excreted by the body."[296], [297]  The CDC tells us that in 1967 the "mumps vaccination was licenced." [298]  However, 22 years later, in 1989, the Urabe strain of the Mumps virus was removed from Canadian vaccines because of a meningitis outbreak. Trevor Gunn cites that during this time in the UK:"cross linking laboratory and hospital reports to vaccination records records, the [perceived low risk from meningitis from this particular vaccine] rose to between 1 in 4000 and 1 in 21,000."These figures led to the removal of this strain in the UK by 1992.  (From the Parliamentary office of Science and technology, "Vaccines and their future role in public health, July 1995, and Dawbarns, Solicitors, Kyngs Lynn,  MMR and MR Factsheet)Measles VaccineA study published in 1994 in the Archives of Internal Medicine evaluated all U.S. and Canadian articles reporting measles outbreaks in schools and found that, on average, 77 percent of all measles cases in these outbreaks were occurring among vaccinated individuals. The authors concluded that "the apparent paradox is that as measles immunization rates rise to high levels in a population, measles becomes a disease of immunized persons."[299]One of the reasons for the resurgence of measles infection is that the antibody response to the vaccine virus is only temporary. One study shows that four years after MMR vaccination, measles antibodies fall below the putative protective levels in 28 percent of children and are no longer present in another 3 percent of vaccinees.[300] Experimenting with high-potency vaccines produced even poorer results.[301]These are just samples of the numerous studies showing that the supposed protection offered by the vaccine is short-lasting. By contrast, natural immunity-that derived from contracting the disease-is permanent and is transferred from mothers to the babies in utero through the placenta. At birth, babies born from mothers who have had the disease are protected from the infection during their first year of life by the presence of a high concentration of natural antibodies circulating in their blood. Measles vaccination, on the other hand, induces lower antibody titers than does natural infection. Neutralizing measles antibodies passed by vaccinated women on to their newborns disappear rapidly, leaving the babies susceptible to the infection in their first year of life, when they are more at risk of complications.This difference in infants' immunity levels is reflected in a 1995 study published in the journal Pediatrics. Researchers found that 71 percent of 9-monthold infants and 95 percent of 12-month-olds had no detectable neutralizing measles antibodies in their blood. All infants with detectable measles antibodies at 9 or 12 months had mothers born before 1963, before the vaccine era.[302]Measles infection is still a severe disease in adults. A study published in theAmerican Journal of Medicine in 1993 shows that, of 68 patients over 14 years old who developed measles, 33 required hospitalization. Of these, nine were admitted to the intensive care unit, six required mechanical ventilation, and two died. The authors concluded: "Measles in adults may result in severe, life-threatening complications that utilize substantial medical resources. Physicians need to appreciate the clinical presentations and manifestations of severe measles in adults and to provide measles vaccine to nonimmune adults during community-wide outbreaks."[303] Again, immunization has failed to protect children from infection and has created a vulnerable population of infants and adults who are at risk of developing severe complications. What is the remedy proposed? Again-more vaccination!Another problem found with measles vaccination, documented in several studies, is that it produces immune suppression that contributes to an increased susceptibility to other infections.[304] One study shows that immunization with live measles virus vaccine produces transient immune depression in vaccine recipients.[305]Trevor Gunn, BSc, wrote an article to the World Health Organization on the inadequacies he feels regarding the safety claims made by vaccine administrators particularly with regards to measles vaccinations around the world:[306]Mr. Gunn felt he was misunderstood in his letter, by the WHO representative who responded to him, CJ Clements, saying that Mr. Gunn claimed that vaccines provided no safety, when, in fact, Mr. Gunn was only demonstrating the shortcomings in the studies that the WHO used to 'prove' effectiveness of vaccines when he requested that the World Health Organization prove the effectiveness of vaccines before continuing to give them.First of all, he pointed out that studies on effectiveness use sero-conversion, or antibody presence in the blood stream to indicate effectiveness of vaccines.  Mr. Gunn points out that the amount of antibody presence the blood does not correlate with the body's ability to fight illness.  Mr Gunn states,  "in the UK the government health authority quotes figures of the measles vaccine as being 90% effective."[307]Mr. Gunn points out that this does not mean that the vaccine is 90% effective in preventing illness, but it means that it produces antibodies in the patients 90% of the time.  Mr. Gunn calls for more accurate studies that measure the level of disease protection afforded to populations, after they've been inoculated, using cohort groups matched for age, population and disease exposure similarities, etc.  A 1991 Press Release by the CDC entitled:  Immunization Initiative, praises the benefits of immunization and gives a basis for the quoted figure of 90% effectiveness of vaccinations mentioned in the above Trevor Gunn article:The CDC's evidence for "saving countless lives and preventing untold illness and suffering" is as follows: First, they cite a figure that before the use of the measles vaccine in 1963 , between half and one million people had measles per year, from which 500-1000 people succumbed mortally.  We remember here, however, David Francis' point that "improved nutrition and public health measures in children were more important than medical intervention in 1900", at the height of the measles outbreak in America, and although the author claims that measles is making a comeback in recent years, he does not give the figures on how he infers that the number spiked in the late 1980s as compared to the vaccine's effectiveness in first the two decades since its use.He does state, however, "a number of urban epidemics of measles [happened] during 1989 and 1990."  It is important that we examine the numbers of measles cases that were reduced, however, after the introduction of the measles vaccine.  From the Greg Beattie book, "Vaccination A Parent's Dilemma", from 1960-1970, the death rate from measles remains essentially flat.  The CDC report, however, stated that, "in the last 2 years, 45,000 cases of measles and over 100 deaths occurred."  The author cites that, "Almost one-half of all cases have occurred in unvaccinated preschool children."  We do not, however, learn in this article, how many deaths occurred in the un-vaccinated group.The author seems to be using this figure to bolster his argument that measles cases rose as a result of lack of vaccinations.  However, if half of all cases of measles occurred in children who were un-vaccinated, then according to his reasoning measles should not have occurred in a significant number of children who were in fact vaccinated.  Public health officials tend to use the counter intuitive claim that the un-vaccinated children provide a contagious health risk to those who are in fact vaccinated.  This seems to belie the whole premise that the vaccination is supposed to protect the child who has been inoculated.  There seems to be some magical thinking with some public health officials regarding the so called, herd immunity-that it only works if all or most children are vaccinated.We note here especially, the two year period following the 1963 introduction of the measles vaccine, that David  Francis stated that the childhood decline in mortality rate was still, "essentially flat," as noted in our paragraph above.  The CDC is proud of the figure that measles deaths were reduced from 4 million per year throughout the 20th century to 37 in 2004.[1]  Trevor Gunn notes, however, that other public health factors play a significant role in outcomes of disease in third world countries.In another report from the WHO on a previously mentioned project in Bangladesh, Gunn points out that in one area, the study showed 36% effectiveness, and another area showed 46% effectiveness.  This was due, the WHO said, to a local epidemic of diarrea which affected the outcome of mortality.  In addition to Mr Gunn's assertions, the WHO's defense also points out the weakness of a one -point solution to a region where childhood mortality is caused by a host of factors, including the main one, (which is lack of nutrition and clean drinking water.)  Another study, E. Holt, et al from the Journal of Pediatrics, Vol. 85, No 2 pp188-194, February 1990[308] studied measles outbreaks in a particular area in Tahiti.  Although the study was nine months in length as opposed to the 10 months in the previous study, it showed greater effectiveness in death reduction than the previous Bangladeshi study.  Dr. Gunn suggests that the paper may be manifesting the common trait among many vaccine cohort studies that he quotes from the Lancet, "gains in survival of a vaccinated group tend to diminish over time to approach a survival rate of unvaccinated individuals"[309]. (The Lancet April 4, 1981 765).Mr. Gunn points out the difficulties with several of the third world studies with regards to vaccine effectiveness in measles and other illnesses:  In the study, P. Aby, et Al, Pediat Infec DisJ 8: 197-200, 1989[310], Gunn tries to answer whether the measles vaccination would lead to greater or fewer deaths, due to the benefits provided by measles in the form of natural immunity in developing countries.  While this is a good question ideally, points out Mr. Gunn, the experiment was poorly carried out:  Although the study claims that the vaccine prevented 30% of measles death, the methods of the paper reveal that the control group was not a nonvaccinated group, but included children who did not sero-convert, and so were assumed to have no immune response to the vaccine.  In this case, then, we would not know whether deaths in the control group were due directly to the vaccine, due to lack of effectiveness of the vaccine, or due to lack of natural immunity provided by the measles itself.In another group of people in this study, 15 out of 123 did not have antibody conversion after vaccination, so their results were excluded as well.  Three of this group actually died.  In this case, then, we do not know the cause of death of those who died, and we still do not find out if those remaining 12 who did not register measles antibodies in their blood, were prevented from getting measles at all.In referring to a paper by Clemens et al, American Journal of Epidemiology, Vol 128, No. 6 1330-39[311], Mr. Gunn complains that the cohort group of the study was cherry picked for people who did not have a history of measles.  Mr. Gunn pointed out that this group may have been less likely to die either from measles in general, or may in general be heartier than the people who were selected against in the study.Gunn points out that : "In the UK, over 95% of the mortality had occurred before the introduction of the measles vaccine."  In addition, therefore, in a developed country, it is difficult to assess the particular role in health prevention vaccination plays, because specific tests have not been developed to test vaccination related disease prevention.  He also states that it must be important to assess the risks of any new medical product administered to the children of an entire population.  He points out the hypocrisy of such organizations as the American Academy of Pediatrics, whose officials claim that, "the benefits of immunization far outweigh the risks," without in reality examining the actual safety of these vaccines.Gunn points out that there is evidence which links inoculation with illness: The Lancet, Vol. 345, April 29, 1995, shows that there is a link between Crohn's Disease and the Measles vaccination: the manufacturer's label includes the possible adverse effects:  "fever, rash, coryza, pharyngitis, bronchitis, convulsions, encephalitis, thrombocytic purpura, and even death." Although some researchers point to good news, "specifically it has been shown that children contracting measles were less likely to suffer from allergic conditions such as asthma, eczema, and hayfever," (Lancet June 29, 1996)  Gunn also points out that infection may cause deleterious effects without the usual measles rash, causing, "sebaceous skin diseases, degenerative diseases of bone and cartilage, and certain tumours."  He states that the Lancet study, January 5, 1985 suggests that interference with the body's own symptomology by repressing measles rash symptoms could in fact, interfere with the body's ability to fight the illness altogether.  Gunn's rationale for bolstering this idea is the study he mentions from the (American Journal of Medicine, Volume 68, pps 344-355, 1980) that people are more likely to die from an infection if they are unable to produce a fever in response to it.  Mumps VaccineAseptic meningitis has been epidemiologically associated with receipt of the mumps vaccine.[312] In 1989, it was finally determined that it was the strain of virus used in the vaccine that caused mumps meningitis. The virus isolated from patients who developed meningitis 21 days after injection was identical to that used in the vaccine. Aypical mumps contracted after receipt of the vaccine is another problem. In 1980, reports surfaced of atypical mumps in previously vaccinated children, with symptoms including fever, appetite loss, nausea, and a generalized rash. The atypical mumps occurred when wild natural mumps virus circulated among unvaccinated children-a normal event associated with immune system development in humans. All the children contracting atypical mumps had been injected with viral vaccine five to seven years earlier.Concerning the mumps vaccine's effectiveness, the scenario with mumps is very similar to that with measles. There are several studies reporting outbreaks of mumps occurring in populations with virtually complete vaccine coverage. Cheek et al., for example, writing in the Archives of Pediatric and Adolescent Medicine, report a measles outbreak in a highly vaccinated (more than 95 percent) high school population. Fifty-three of 54 students who got the disease were vaccinated.[313]Another study reported an outbreak of mumps in a Tennessee school with 98 percent vaccine coverage, where 67 of 68 students who got mumps had been previously vaccinated. Thus, mumps cases in this instance were attributed mostly to vaccine failure.[314]While mumps infection is a largely benign disease when contracted during childhood, it becomes more dangerous in older children and adults, who are more susceptible to severe neurological, testicular, and ovarian complications from the infection. It is alarming to see that vaccination is clearly shifting the occurrence of this disease from young children toward those who are older.[315]Perhaps the boldest statement on the efficacy of the mumps vaccine in preventing the disease comes from the authors of a study conducted in Switzerland. They conducted an epidemiological analysis of mumps cases there and found a fivefold increase in the number of mumps cases from 1990 to 1993, especially in vaccinated children. Among the authors' conclusions was: "The Rubini [mumps] strain vaccines, which are the most commonly used in Switzerland, seem to have played an important role in the clear increase in mumps cases since 1990."[316]Rubella VaccineUnfortunately, rubella vaccination is similar to measles and mumps immunization in terms of lack of efficacy in preventing the targeted disease. A study published in the European Journal of Epidemiology shows that after the Swiss began a rubella mass vaccination campaign in 1985, the incidence of rubella remained unchanged during the period from 1987 to 1992. The authors concluded: "MMR mass vaccination has not interrupted the circulation of rubella virus in Switzerland."[317]Also, a study published in the Journal of the American Medical Association in 1981 shows that 15 years after receiving rubella vaccination, one in 11 children lost protection from the vaccine and became susceptible to re-infection.[318] This is particularly worrisome because rubella infection is especially dangerous when contracted during pregnancy, since the fetus may develop malformations if exposed to the virus. Again, the lack of permanent immunity offered by vaccination is creating serious problems down the line.Viera Scheibner has looked in depth into the research on rubella, and informs us: "As Cherry (1980) wrote, despite distribution of over 83 million doses of rubella vaccine since 1969, there were periodic upswings in incidence. There was also a shift in the age groups susceptible to rubella. 'Essentially, we have controlled the disease in persons 14 years of age or younger but have given it a free hand in those 15 or older.' "[319], [320]Scheibner adds: "In August 1991, the Institute of Medicine released a report on adverse effects of pertussis and rubella vaccines. The evidence indicated a causal relationship between RA 27/3 rubella vaccine and acute arthritis in 13 percent to 15 percent of adult women. Also some individuals were shown to go on to develop chronic arthritis."[321]FURTHER READINGS: Articles associate the MMR vaccine with adverse reactions affecting the nervous system,[322], [323], [324], [325], [326]the GI tract,[327] and joints.[328], [329], [330]In Part 3: The smallpox and rotavirus vaccines, provocation diseases associated with vaccines, economic, political and legal issues, and the right to refuse vaccination.Vaccination: Pain, Profit, and Politics - Part 3By Gary Null, Ph.D., and Martin Feldman, M.D.In Parts 1 and 2 of this series, we examined factors countering our beliefs that vaccines are safe and effective. We also discussed the effects of specific vaccines, including those for diphtheria, pertussis and tetanus, polio, chickenpox, hepatitis B, and measles, mumps and rubella. In this final installment, we look at the smallpox vaccine, the withdrawn rotavirus vaccine, and the provocation diseases associated with vaccines. Finally, we discuss the economic, political and legal issues of vaccination, the right to refuse vaccination, and the need to achieve freedom of choice.The Smallpox VaccineSmallpox was the impetus for the invention of the vaccine in the New World.  It "was introduced into the Americas in the 16th Century and Australia in the 18th Century.  It had been present in Africa, Asia and Europe since at least 400 BCE."[331] It was said to have traveled along trade routes and to have erupted every ten years.  Variolation, the process of sharing a small bit of infected matter with an uninfected person started in Africa and was present in Europe in the 18th century.  From the US National library of Medicine, "In contrast to Asians and Africans who inoculated by blowing dried smallpox scabs up the nose, Europeans and their American cousins tended to inoculate through a puncture in the skin."[332]  Some, however, died as a result of the procedure, and epidemics were also started this way.  It is also widely known that measles infections in families were 'gotten through with' by making sure that if one child got telltale signs of swollen glands and fever, the other children in the home or the neighborhood were invited to share a bedroom, in order to spread the infection and get it over all at once.  Even in the late      20th century, well into the 1970's, chickenpox was shared in much the same way, allowing children in a family or a neighborhood to get through the infection, with the assumption that it could cause greater complications as an adult, and that infection would not likely occur twice.  It was Jenner who first popularized the vaccine program with his smallpox vaccine. A close look at history reveals that the procedure never worked, however. Neil Miller, a medical research journalist, natural health advocate and author of Immunization Theory Vs. Reality: Expos on Vaccinations,[333] summarizes the story, as follows: "In 1796, Jenner came on the scene saying that when dairy maids caught cowpox they could no longer catch smallpox. His medical colleagues disputed his claims, as the research of the times indicated numerous cases of dairy maids and other individuals catching cowpox and coming down with smallpox. Yet Jenner persisted, and he published a treatise on this idea in 1798. He called his treatise Inquiry, and became famous for it."Edward Jenner, a country doctor and a Fellow of the Royal Society formulated the idea of vaccines fashioned after the old country tale that those who got cowpox were protected from smallpox. In order to test this theory, on May 14, 1796, he removed some fluid from Sarah Nelmes' hand which had cow pox lesions, and injected it into the arm of James Phipps, who was a healthy eight year old boy. Later, Jenner injected the boy with smallpox.[334] When James did not come down with smallpox, Jenner concluded "that the cow-pox protectsthe human constitution from the infection of smallpox"[335]   He subsequently self-published An Inquiry into the Causes and Effects of the Variola Vaccine in June 1798 detailing the James Phipps experiment along with other observations. Jenner's cowpox vaccine consisted of dry or liquid pus taken from the ulcers of cows or humans with cowpox or from the pustules of horses with horse-grease, an infection of the heel. Inoculation involved cutting a small hole into the skin and inserting the virus from the pus into the arms of the patients with a lancet.  Then Jenner's method of transferring a small amount of infected smallpox material from one person to another, as we learned earlier, is called variolation, and there were many variations of this procedure.  Critics noted that variolous inoculation, however, could cause bad cases of smallpox, so intricate methods were developed to administer it:  Typically, a lancet was used to insert variolous material into a small cut of the skin. The variolous matter was taken from someone going through the earliest stage of a mild smallpox vesicle growth in which there was barely any fluid. This material was then inserted into one patient. Subsequently when mild symptoms occurred, new material was taken from that patient and then used on other patients. The process of collecting variolous matter was continued from arm to arm.[336] A smallpox epidemic in France revealed that the inoculation failed badly to protect the patients of Dr. Gatti in France. As a result, Paris outlawed these inoculation practices. [337]Jenner, however, espoused a milder technique of variolation: "I have the strongest reason for supposing that if either the punctures or incisions be made so deep as to go through it and wound the adipose membrane, that the risk of bringing on a violent disease is greatly increased. I have known an inoculator whose practice was to cut deep enough (to use his own expression) to see a bit of fat," and there to lodge the matter. The great number of bad cases, independent of inflammations and abscesses on the arms, and the fatality, which attended this practice, was almost inconceivable; and I cannot account for it on any other principle than that of the matter being placed in this situation instead of the skin. It was the doctor's practice to make as slight an incision as possible upon the skin, and there to lodge a thread saturated with the variolous matter... it has been proved that variolous matter, when much diluted with water and applied to the skin in the usual manner, will produce the disease." Creighton, a 19th century historian put it this way, "The matter for inoculation was not taken from a natural or accidental eruption of smallpox; it was taken from the local pustule alone of an artificial inoculation, and it was taken from the very earliest period of the local pustule at which any fluid could be got at all, or "just before the commencement of the eruptive fever."[338]Critics of variolation cite that over scrupulous variolators could actually fail to give any inoculation at all: By that means, as [Salmade], a French variolator of the time reports, " the smallpox becomes at length weakened to the point of nullity, so that the last inoculations are without effect."[339]  Thus, weakened variolation might not cause any illness, but it also might not engender any immunity, either.[340]Jenner's early efforts to coerce his colleagues to his way of thinking were "ineffectual; his brethren were acquainted with the rumor, but they looked upon it as one of those vague notions from which no accurate or valuable information could be gathered, especially as most of them had met with cases in which those who were supposed to have had cowpox had subsequently been affected with smallpox."[341]Creighton added, "Certainly for those who knew by inspection what the pox of the cows' teats was, and most of all for those who had suffered the painful and often obdurate ulcers on their own hands, there would be no suggestion of real likeness to smallpox, or of the one disease being in any way related to the other. It was the jingle of the names that brought the two together in the first instance."[342] The "diseases themselves were totally unlike. It was just because Jenner had no profound sense of these empirical realities that he went blundering into visionary nonsense in the first instance, and at length into systematic mystification and chicane[ry]."[343]  "In the monograph by Nicholas Massa, of Venice, he says they [smallpox pustules] occurred over the whole body-on the limbs, on the face and head, and amongst the roots of the hair. In his particular description we find such terms as elevated, tumid, moist; red, livid, whitish; small, dry, itching ; broad, flat, soft. They came out comparatively early in the disease (second or third week even), and their outbreak was often the signal for the notorious pains in the head and limbs to abate."[344]  Cowpox, on the other hand, was the ulcerous pox of the cows' teats, which can infest the skin, namely the hands, of those who milk the cows. Those infected will also feel a flu-like illness often accompanied with swollen and painful glands in the armpits. Horse-grease, another illness which Jenner conflated into his smallpox theory affected the hocks of horses causing inflammation and swelling.  Contact with the diseased heels created an infection with burning white blisters which later become painful corroding ulcers.[345]  Clayton, a veterinarian in Jenner's county spoke of the separate nature of horse grease from cowpox:  He wrote that he was "extensively employed, particularly in curing the [horse-]grease" and also elaborated that "the grease is most prevalent in the winter, at which time he has never known the cowpox to occur... [also] he could not recollect ever to have had horses with the grease and cows with the cowpox under care at the same farm... [Furthermore] he is very certain he has frequently had cows with the cowpox, where no horses whatever have been kept."[346] However, Jenner did not see it that way. In the opening of the first chapter of his Inquiry, he wrote that horse-grease "is an inflammation and swelling in the heel, from which issues matter possessing properties of a very peculiar kind, which seems capable of generating a disease in the human body,...which bears so strong a resemblance to the smallpox that I think it highly probable it may be the source of the disease.Jenner's Inquiry paved the way for universal acceptance of vaccination as a gold standard of modern medicine's ability to protect us from disease. Jenner's previous "medical papers" however, were spurious. Previous to his papers on cow-pox, one was on the subject of preparing a tartar emetic, and an another was on the observation of calcified coronary arteries of the heart in a case of someone who suffered from angina pectoris. His "philosophical papers " are represented solely as observations on the cuckoo, in the Philosophical Transactions for 1788." [347] It was this paper on the cuckoo, which was essentially a piece of fantasy,  that propelled Jenner into the Royal Society which was chaired at that time by Sir Joseph Banks, a friend of Jenner's, a year later.[348]Jenner's Inquiry paper involved about 2 years of research and one single experiment involving cowpox and smallpox inoculations on the one patient, James Phipps. His status as a fellow of the Royal Society and his strength as a salesman were the reasons for his success in twisting myth into science. Dr. Baron, Jenner's own biographer, wrote that Jenner frequently mentioned cowpox innoculation immunity to smallpox in the meeting at the Society which involved Fewster of Thornbury, the chief authority on cow-pox. Dr. Charles Creighton M.A. M.D, professor of Microscopic Anatomy at Cambridge, wrote the section on 'Vaccination' in the ninth edition of the Encyclopedia Britannica, published in 1888. A year later, he also wrote JENNER AND VACCINATION - A Strange Chapter of Medical History, a detailed history of Edward Jenner's professional life.  Creighton stressed that one danger in using variolous inoculation as a measuring stick for smallpox infection was that the cowpox vaccine "caused a swelling and obstruction of the absorbent glands in the armpit and neck, and to that extent made them incapable for the time, and in some cases for long after, of taking up and passing into the lymphatic circulation another virus inoculated under the skin at the same place... Apart from the swollen and clogged state of the absorbent glands after cowpox [inoculation], the mere presence of a sore of any kind on the arm served to divert and obviate the full action of a new infection"[349]Many of the children used as test subjects were from poor households, orphanages and foundling hospitals. These children often have chronic swelling of the lymphatic glands. Even Jenner noticed the tendency to resist variolous inoculation.  He said in his Inquiry, "There are many who, from some peculiarity in the habit, resist the common effects of variolous matter inserted into the skin."[350]He did not mention who these people are, nor did he feel the need to stop using the variolous test as barometer for smallpox immunity since he discovered some people are immune to the variolous test. James Phipps, living proof of Jenner's smallpox immunity, very likely fell into this category. After writing the Inquiry, Jenner noted that James "has been very unwell lately, I am afraid that he got tubercles in the lungs. He was recently inoculated for the smallpox... for the twentieth time, all without effect."[351] Being a test subject with numerous cowpox and variolous inoculations and having tubercles in the lungs are signs that James Phipps likely had swollen lymphatic glands too. Creighton elaborates in that "an eruption after cowpox has the same significance as an eruption after the pox proper; it is a secondary effect, or a sign that the constitution has been touched by the infection. A person still under the influence of the secondaries of cowpox would not be a likely subject for smallpox engrafted on the top of it... [Furthermore,] the mere presence on the skin of spots or pimples or vesicles or blebs would hinder the full evolution of smallpox by inoculation... The presence of any common eruption, even itch, was well known to prevent the cowpox itself from taking. Jenner began, about the year 1804, to explain the failure of cowpox by an ambitious doctrine of "herpes"... it had this grain of truth in it, that an infection inserted under the skin would not have a fair chance of being absorbed if the skin were already engaged with an eruption even of the most ordinary kind. In so far as that was a plea for the failure of cowpox, it was a plea for the failure of inoculated smallpox." [352]Ironically, the variolous inoculation was later used as one of the many excuses for cowpox vaccine failure and subsequently played a part in creating the first English mandatory vaccination program in 1853. The idea is that variolous inoculations were, in addition to causing the smallpox revival, encouraged people to ignore the 'true protector', cowpox vaccine. In 1840, England, spurred on by the Medical Society, passed a law to protect the public from variolous inoculation under penalty of imprisonment. The strict penalty was made by Mr. Wakley, editor of The Lancet.  He blamed variolous inoculation for 17,000 smallpox deaths in one year, and he also added that smallpox would disappear if variolations were prevented and vaccination adopted.[353]There was, however a general revival of variolous inoculations over cowpox vaccination. Despite the fact that the public had 40 years of Jenner's vaccination, smallpox was still a continuous plague. Creighton wrote, "In the disastrous epidemic among children at Norwich in 1819, ...due to overcrowding of the town by a great influx of families from the country while trade was brisk, the failures of vaccination were so obvious to those directly concerned that the common people insisted on having their children inoculated in the old way to save them from the contagion."[354]In 1853, the Compulsory Vaccination Act was instituted, mandating vaccination for children. Built on the precedent of the law that made variolation illegal in Great Britain in 1840, the new idea, propagated by the Vaccination Committee, was that preventing smallpox required the cowpox vaccine.[355]Yet despite the vaccinations, from 1857 to 1859, the smallpox epidemic killed 14,244 people. From 1863 to 1865, a second outbreak claimed 20,059 lives. A more stringent compulsory vaccination law was passed in 1867, and those who evaded inoculation were prosecuted. An intensive four-year effort to vaccinate all people between the ages of 2 and 50 resulted in 97.5 percent of the population being vaccinated. The following year, though, England experienced its worst-ever smallpox epidemic; 44,840 lives were lost. Overall, from 1871 to 1880, during this period of compulsory vaccination, the death rate from smallpox leapt from 28 to 46 per 100,000.The early years of the 19th century in Europe saw a noticeable reduction of the epidemic outbreaks of the all disease including smallpox. This fact gave ammunition to the vaccine establishment. In 1904, Dr. Charles Ruata, M.D. pointed out the specifics in the rise and fall of diseases in England in the period before and after the turn of the 19th century. Using data from the Reports of the Royal Commission, who have a pro-vaccination view, and from the annual reports of the Registrar-General, he made twelve charts, "each showing the comparative rise or fall of small-pox mortality and other diseases in various places and under different conditions; and all these without exception demonstrate either that vaccination has no effect whatever, or that it tends to increase rather than decrease small-pox mortality."[356] His smallpox diagram of London shows that the disease "decreased during the ten years before vaccination at very nearly the same rate as it did in the ten years after vaccination...General mortality also decreased after 1800 more rapidly than before 1800. Yet the Royal Commissioners declare that there was nothing but vaccination to produce the decrease of small-pox, and that there was no improvement in sanitation in the beginning of the nineteenth century, as compared with the latter part of the eighteenth century, to account for the difference."[357]Ruata cited five primary reasons for the decline of most diseases in London after the 1700's. First, diseases, especially during epidemics, are much higher in cities. Many city dwellers moved to newly built "West-end squares and suburbs." Secondly, sanitation on the streets was improved, while the roads were better maintained. That lead to the third reason; better roads allowed more fresh meat, vegetables and milk to be brought into the city, which gave the inhabitants better nutrition. The fourth reason was an improved water supply. Finally, the dead were not rotting in the city anymore as cemeteries were built outside London while many city graveyards were permanently closed. He added that these results strikingly decreased, "the death-rate in a number of the most fatal diseases (as recorded in a Table by Dr. Farr, reprinted in the Third Report of the Royal Commission) to fully one-half in 1801-10 as compared with 1771-80; an amount of improvement which has never occurred in any similar period during the whole of the 270 years for which we have official statistics."[358]          One of the greatest smallpox epidemics in Europe happened between 1870 and 1872. By this time, cowpox vaccination was established with many countries adopting mandatory vaccination in at least some form. In German Prussia the official death count was 124, 948. No records were kept for the vaccinated or unvaccinated although there was some evidence that the vaccinated were at least comparable to the unvaccinated.[359] In England and Wales, the official registration report showed 42,210 deaths from 1871 to 1872. This is a staggering figure considering the fact that England established a mandatory children's vaccination program in 1853 under the strict penalty of imprisonment for violators.[360]  Leicester, a manufacturing town in England with 200,000 inhabitants, offers us a great insight into the nature of cowpox vaccination. Having suffered greatly in previous epidemics, Leicester was one of the most completely vaccinated towns in all of England up to 1872. According to Ruata, in 1871, the "small-pox deaths during that year...[were] more than 3,500 per million of the population, or about one thousand per million more than the mortality in London during the same epidemic. Here an almost completely vaccinated community suffered more than unvaccinated and terribly unsanitary London, on the average of the last forty years of the eighteenth century." After their horrible experiences, Leicesterians refused vaccination even under the threat of imprisonment. By 1890, their ratio of vaccinated versus unvaccinated was reversed to only 5 percent vaccinated. Doctors scolded them: "that once small-pox was introduced it would run through the town like wildfire and decimate the population. Yet it has been introduced again and again, but it has never spread; and from that day to this [1904], no town in the kingdom of approximately equal population has had such a very low small-pox mortality as this almost completely unvaccinated and--as the doctors say--unprotected population!"[361]Modern smallpox vaccinations include the following ingredients: " live vaccinia virus, with 'some microbial contaminants,' according to the Working Group on Civilian Biodefense, polymyxcin B sulfate, streptomycin sulfate, chlortetracycline hydrochloride, and neomycin sulfate, glycerin, and phenol -a compound obtained by distillation of coal tar, and vesicle fluid from calf skins."[362]The CDC website admits that the smallpox vaccine is not made from smallpox virus: "The vaccinia virus is the 'live virus' used in the smallpox vaccine. It is a 'pox'-type virus related to smallpox. When given to humans as a vaccine, it helps the body to develop immunity to smallpox. The smallpox vaccine does not contain the smallpox virus and it cannot cause smallpox."[363] Juniors at Stanford University, Jennifer Aguayo and Jessica Caldern, write, "Vaccinia virus is a big mystery in virology. It is not known whether vaccinia virus is the product of genetic recombination, or if it is a species derived from cowpox virus or variola virus by prolonged serial passage, or if it is the living representative of a now extinct virus."  The university of Florida College of medicine information page writes something similar: "Vaccinia is the virus that was used for vaccination against smallpox. Its exact origin is unknown, however, as it does not appear to be related to any other known pox virus. Some people think that it is a recombinant of smallpox and cowpox, while others think that it may be a derivative of horsepox, a virus that no longer exists (if it ever did)."Historians cite improvements in America in the 20th century to the smallpox vaccine which included the pedal injection system for mass injections, a special 'bifurcated needle' in 1961 that penetrated the skin twice in one injection, and the all out mass eradication effort, called E2  which was considered to have wiped out smallpox on a grand scale in Sierra Leone.[364]  The CDC notes that smallpox was reduced from an average of 29,005 deaths per year during the 20th century to 0 cases on 2004.  In 1971 the CDC states that "small pox vaccination was ended in the United States." [365]Despite this fact, in 2001 as a result of terrorist threats, "the United States established a plan to reintroduce Smallpox vaccine if necessary."[366]Edward Jenner is indeed a man who changed the world. The current history displays a Renaissance man of great integrity, but with the bogus variolous tests and cries of spurious cowpox, Jenner managed to create a myth of smallpox immunity from his cowpox vaccines. That myth became a Teflon medical dogma. In spite of the overwhelming evidence of cowpox vaccination failures during the many smallpox epidemics, vaccination was still propped up as a gold standard of medicine by an industry that would not let it die. The result of the vaccine establishment's tenacity is the resurgence of the boast that vaccination eliminated smallpox today. A vaccine is created only for one purpose and one alone; that is to provide immunity to the vaccinated from the attack of the single disease that it was made to defend against. If cowpox vaccine works, there should not even be one death from smallpox in the vaccinated. Jenner stated in his Inquiry, unequivocally, "that the person who has been thus affected [by vaccination] is forever after secure from the infection of the smallpox." The number of smallpox deaths in the vaccinated in the past 200 years is also unequivocal; truthfulness aside. Proper hygiene, sanitation and better living conditions are the true conquerors of smallpox.Rotavirus Vaccine  Rotavirus is a common virus that usually causes mild and selflimiting diarrhea in children. In 1998 Wyeth Laboratories, Inc., of American Home Products, released RotaShield, a new vaccine against the infection. Since four major types of rotavirus cause disease in humans, the vaccine was tetravalent, consisting of genes from four viral strains. The Advisory Committee on Immunization Practices (ACIP), American Academy of Pediatrics (AAP) and American Academy of Family Physicians (AAFP) recommended universal use of RotaShield for healthy infants at 2, 4, and 6 months of age. (Although the AAFP had been in favor of voluntary vaccination or vaccination of high-risk infants only, the ACIP had wanted the universal recommendation.) A year later, though, the vaccine was removed from the market after 99 cases of bowel intussusception-a bowel obstruction in which one segment of the intestine telescopes inwardly into another-and two deaths were reported to the Vaccine Adverse Event Reporting System.Bowel intussusception is a severe condition that often requires surgical intervention and can lead to death in the absence of prompt treatment. For example, of the first 15 reported infants who developed bowel intussusception, eight had to have surgical reduction, including one infant who had 7 inches of intestine removed. (1) These 15 cases, it should be noted, constituted but a small fraction of the actual number of intussusception cases caused by RRV-TV, as the new vaccine was called. According to the Morbidity and Mortality Weekly Report of July 16, 1999, "because reporting to VAERS of adverse events following vaccination is incomplete, the actual number of intussusception cases among RRV-TV recipients may be substantially greater than that reported."[367], [368] And so it was. As soon as the Centers for Disease Control and Prevention (CDC) began warning doctors about the possibility of this complication, cases of bowel intussusception started being reported around the country. This is yet another important example of how vaccine complications, unless specifically looked for, go unnoticed by the medical community and thus by society at large.After it was approved, an estimated 1 million U.S. infants were vaccinated with RotaShield. What is even worse about the history of the rotavirus vaccine is not only the fact that it caused the hospitalization and deaths of several children, but the fact that prelicensure trials had already demonstrated that it caused bowel intussusception at rates 30 times higher than those expected. This is what emerged from analysis of prelicensure trial data by the Association of American Physicians and Surgeons (AAPS).[369]Is the Approval Process Tainted? So here is the question: If the fact that the vaccine could cause a potentially lethal complication was already known, why did the FDA approve it? Why had nobody warned doctors to watch for this complication? Indeed, these and more questions prompted the AAPS to request a Congressional investigation of the vaccine approval process. As Dr. Jane Orient, executive director of the AAPS, writes in a letter to Representative Dan Burton, "The situation with the rotavirus vaccine may be a clue to a far more serious problem with the vaccine approval process."Dr. Orient makes the important point that "Decisions about vaccines given to children should be made by parents in consultation with the child's attending physician, not mandated by a small group of 'experts' with minimal accountability."[370]Lessons of HistoryAs we've seen again and again, there has been a direct relationship between vaccinations and an increased incidence of the diseases they supposedly prevent. This contradiction has prompted several researchers to conclude that vaccines are neither safe nor effective.          In a 1926 British Medical Journal article, a Dr. Parry asks why vaccine statistics reveal a higher death rate among the vaccinated: "How is it that smallpox is five times as likely to be fatal in the vaccinated as in the unvaccinated? How is it that in some of our best vaccinated towns, for example, Bombay and Calcutta, smallpox is rife, while in some of our worst vaccinated towns, such as Leicester, it is almost unknown? How is it that something like 80 percent of the cases admitted into the smallpox hospitals have been vaccinated, while only 20 percent have not been vaccinated? How is it that in Germany, the best vaccinated country in the world, there are more deaths in proportion to the population than in England? For example, 28 deaths in England in 1919 per 100,000, and 707 in Germany? What is the explanation?"[371]Tuberculosis. Trevor Gunn makes the point that "Improvements in living standards have almost as much an effect on reducing mortality as that predicted vaccination." Mr. Gunn responded to the allegations by the World Health Organization that double blind studies were unethical because they limit the control group from receiving the benefits of life saving immunity. First of all, he pointed out that double blind placebo controlled trials of tuberculosis vaccine were initiated after some children died after receiving inoculations from a contaminated batch of vaccines.  The results of the double blind study showed no increase in immunity from receiving the vaccination, and possible increase in actual tuberculosis cases for the cohort that did in fact receive the inocculations. Despite this fact, Gunn says the vaccine has continued to be used.  Gunn also points out other flaws in the tuberculosis studies, which he feels ought to be taken into account in all studies on vaccination effectiveness:1)That there were not standards for diagnosis, so that before and after comparisons of illness were not accurate.2)Studies did not take into account the importance of public health factors when examining illness related causes.          In addition, those who take issue with universal immunization programs point out that the programs don't discriminate between children who may benefit from a certain vaccine and those who might be hurt by it. Babies are given blanket immunization regardless of their previous or current state of health and regardless of their varying susceptibilities to side effects. Ideally, there should be a much more selective vaccination system, with parents given complete information so they can make up their own minds as to whether the risks associated with a particular procedure outweigh its potential benefits. Just as different races are known to suffer disproportionately from various allergies and food sensitivities, studies also indicate that they may experience different reactions to vaccines.Provocation DiseaseOne of the most hazardous and insidious effects of vaccination lies in its potential to induce other forms of disease, a phenomenon known as provocation disease.[372], [373], [374], [375], [376], [377] The mechanisms that cause this to happen are unclear, although many scientists believe that latent viruses-those already existing within a person-may be stimulated by vaccinations, and that this may be enough to activate a particular illness. Vaccination, therefore, may not be the sole cause but rather the final trigger for an illness.In his book Vaccination and Immunization: Dangers, Delusions & Alternatives,[378]Leon Chaitow states that there is no way of knowing when such latent or incubating situations may be operating, and therefore no way of knowing when a vaccination may produce this sort of provocation.[379] He goes on to warn that provocation of a latent virus is a potentially dangerous possibility with every vaccination procedure.Many diseases thought to be caused at least partially by vaccinations do not surface until years later, by which time it is difficult to prove a connection. Some of the relationships between vaccines and the specific conditions they provoke are discussed below.Allergies. According to Dr. Harris Coulter, co-author of A Shot in the Dark[380] and author of Vaccinations, Social Violence, and Criminality, among other experts,[381]says that vaccines and allergies are clearly connected. "What does allergy mean? It means that your body is ready to react very, very quickly when exposed a second time to a substance to which it is allergic. If you are allergic to ragweed, [a small amount] of ragweed will start you sneezing. Now, if you vaccinate a person against pertussis or some other bacillus, you are making that person allergic to that bacillus. That's what being vaccinated actually means. It means you are allergic to that bacillus, in the sense that your body will react very, very rapidly if exposed to that bacillus a second time."Sudden Infant Death Syndrome (SIDS). Sadly, many studies have shown vaccination to be a cause of sudden infant death syndrome. Reports Alan Phillips, founding director of Citizens for Healthcare Freedom, Durham, N.C.: "One study found the peak incidence of SIDS occurred at the ages of 2 and 4 months in the U.S., precisely when the first two routine immunizations are given, while another found a clear pattern of correlation extending three weeks after immunization. Another study found that 3,000 children die within four days of vaccination each year in the U.S. (amazingly, the authors reported no SIDS/vaccine relationship), while yet another researcher's studies led to the conclusion that half of SIDS cases-that would be 2,500 to 5,000 infant deaths in the U.S. each year-are caused by vaccines."[382], [383], [384], [385]          According to Viera Scheibner, a retired research scientist, "Baraff et al. (1983) investigated 145 SIDS victims who died in Los Angeles County between January 1979 and August 1980: Fifty-three of these babies had received a DPT immunization, 27 within 28 days of death. Six deaths occurred within 24 hours and 17 occurred within 1 week of DPT immunization. These sudden infant deaths were 'significantly more than expected were there no association between DPT immunization and SIDS.' "[386], [387]Immunosuppression and Autoimmune Disease. The body needs to experience a full inflammatory response to create immunity, and vaccines do not allow this to happen. Instead, a chronic condition is created that can set the stage for autoimmune disease.In Immunization: The Reality Behind the Myth, author Walene James describes the mechanics involved in vaccines inducing autoimmune disorders: "Live viruses, the primary antigenic material of [some] vaccines, are capable of surviving or remaining latent in the host cell for years, without provoking acute disease."[388]          Cynthia Cournoyer, author of What About Immunizations?, believes that a key principle involved in understanding the many negative effects of vaccines is the fact that the immune system can only tolerate so many challenges, especially before it is given a chance to develop to maturity. "Every child," she writes, "is born with a finite ability to combat disease. This is his total immune capacity. Once a child experiences a particular disease, permanent immunity is extremely efficient, using probably 3 percent to 7 percent of the total immune capacity of an individual. In the case of routine childhood vaccination, it is likely that as much as 30 percent to 70 percent of total immune capacity becomes committed.          "These findings could indicate that a child's immunological reserves are substantially reduced due to standard vaccine programs. Far from producing a genuine immunity, a vaccine may actually interfere with or suppress the immune response as a whole, in much the same way that radiation, chemotherapy and corticosteroids and other antiinflammatory drugs do."[389], [390], [391]          Cournoyer continues, "Although the body will not make antibodies against its own tissues, viruses becoming part of the genetic make-up may cause cells to appear foreign to the immune system, making them a fair target for antibody production....          "Under proper conditions these latent pro viruses could become activated and cause a variety of diseases, including rheumatoid arthritis, multiple sclerosis, lupus erythematosus...and cancer."[392]Activists Speak Out on Vaccine DangersBarbara Loe Fisher, cofounder and president of the National Vaccine Information Center (NVIC), Vienna, Va., has advocated the right of individuals to make informed, independent vaccination decisions for themselves and their children for two decades. She shares her concerns about a number of issues, as do some of her colleagues engaged in the fight against government-mandated vaccines.Problems with Temporary Immunity and Benefits of Childhood Disease. Vaccines provide only temporary immunity, whereas when you get the natural disease you have permanent immunity most of the time. Viera Scheibner writes that "generations of children with this inadequate immunity would grow into adults with no placental immunity to pass on to their children, who would then contract measles at an age when babies are normally protected by maternal antibody....          "Perhaps the most unfortunate thing about the idea of eliminating infectious diseases by vaccination is that indeed there is no need to do so. As pointed out by the group of Swiss doctors opposing the U.S.-inspired policy of mass vaccination against measles, mumps and rubella in Switzerland, 'We have lost the common sense and the wisdom that used to prevail in the approach to childhood diseases. Too often, instead of reinforcing the organism's defenses, fever and symptoms are relentlessly suppressed. This is not always without consequences...' "[393], [394], [395]          Lastly, Scheibner states, "There is no need to artificially immunize our children and ourselves. The body has proper, natural mechanisms to create immunity to diseases. The diseases themselves are the priming and challenging mechanisms of the maturation process leading to the competence of the immune system....[396]The EZ Measles Medical Fiasco. In the mid-1980s researchers from the CDC and Johns Hopkins University started vaccinating babies as young as 4 months old with the experimental high-titer Edmonston-Zagreb (EZ) measles vaccine. Targets were more than 1,500 black and Hispanic babies in Los Angeles and thousands of babies in several Third World countries. The experiment was halted in 1991, after results of several studies showed that female babies receiving the high-potency vaccine had a 95 percent increased mortality rate compared to those injected with the standard measles vaccine.[397], [398]Economic, Political, and Legal IssuesCynthia Cournoyer has noted that vaccines are the only products in the U.S. that are legally mandated to be used by every person born.[399]Barbara Loe Fisher paints an ominous picture of things to come: "As consumers, we can bring very little economic pressure on the system to have that product improved or removed, because all of us are required by law to use it. It's a dream for the pharmaceutical industry involved in making vaccines, because there's no way anybody can say no. It's a stable, ready-made market, and the enactment of the compensation law in 1986 has removed almost all liability for drug companies...."What concerns us most is that there is an electronic monitoring system being put in place by state public health departments with federal funding-they're trying to get it in every child born and monitor his or her vaccination status....          "...If we don't act now, the public health infrastructure is going to get more power to intrude in our lives, intrude in our health care choices. It all comes down to whether or not we, as individuals, are going to fight for the right to make informed health care choices, including vaccination choices, for ourselves and our children, and whether we are going to hold the drug companies and government health officials accountable for the injuries, deaths, and chronic illnesses caused by vaccines they produce, sell, and promote for mass use."[400]          One interesting financial aspect of vaccines involves the federal ACT Compensation Program. An excise tax of $23.50 was tacked onto the price of vaccines in 1988 to fund this compensation program. What this means is that consumers are footing the bill for any injuries or deaths that may result from medical procedures that they are required by law to undergo.[401], [402], [403]          Alan Phillips notes: "[Pharmaceutical companies] have been allowed to use gag orders as a leverage tool in vaccine damage legal settlements to prevent disclosure of information to the public about vaccination dangers. Such arrangements are clearly unethical; they force a nonconsenting American public to pay for vaccine manufacturers' liabilities, while attempting to ensure that this same public will remain ignorant of the dangers of their products."[404], [405]          Vaccine critic Randall Neustaedter concurs: "Profit has always been the goal of vaccine manufacturers. When lawsuits leveled at drug companies began wiping out profits gleaned from the pertussis vaccine, the manufacturers simply stopped production of the vaccine. The United States government stepped in to pay these vaccine-damage claims. Only then did the drug companies agree to resume vaccine production...."[406]Right to Refuse VaccinationA question frequently asked of advocates on the front lines of the freedom-fromvaccines movement concerns legal rights of refusal. According to Fisher, whose book The Consumer's Guide to Childhood Vaccines provides information on this topic, "It is common for hospital and clinic or emergency room staff to ask you about your child's vaccination status. You don't have to provide them with written proof. A verbal answer is satisfactory. However, if you are being questioned closely and feel that you are being pressured into vaccinating your sick child without your consent, you should understand that you have the right to refuse to give permission to have your sick child vaccinated if you believe vaccination at the time will endanger your child's health or life. You may choose to reassure medical personnel that you will consult a private pediatrician for further guidance about vaccination."[407]          One special precaution, Fisher notes, involves pregnant women. "When pregnant women are admitted to a hospital to have a baby, many times while in active labor, the hospital will require that the mother or father sign a paper agreeing to have the baby treated by medical personnel while in the hospital. Signing this paper may also constitute your consent to having your newborn vaccinated with hepatitis B vaccine shortly after birth. Many parents have reported that their newborns are being vaccinated without their knowledge and, when they ask why, they are told they signed a consent form prior to admission agreeing to medical treatment the hospital determined was necessary. Read any consent form you sign carefully. If you do not want your newborn vaccinated shortly after birth, you have the right to sign it after writing in an exception, such as, 'I do not consent to have my child given any vaccinations prior to discharge from the hospital.' Bring this to the attention of the person admitting you and the nursery supervisor and ask to have it printed on the outside of your chart. Some parents take the extra precaution of not leaving the newborn alone with hospital personnel without being able to observe the baby."[408]          In the unfortunate case of an adverse vaccine reaction resulting in medical bills totaling more than $1,000 or injuries lasting longer than six months, parents qualify for benefits under the National Childhood Vaccine Injury Act of 1986 (PL 99-660).[409] Through fiscal year 2001, the National Vaccine Injury Compensation Program had paid $1.3 billion in total awards (petitioner's awards and attorney's fees) for approximately 1,660 compensable petitions.[410]What the Future May HoldFisher believes that if we are concerned about our health and our freedoms, we should be worrying about the future. "I truly believe that unless the public wakes up to what is happening, and starts standing up for their right to be fully informed about vaccines, and their right to make informed independent vaccine decisions, the day will come when we won't have that right. We will be forcibly vaccinated by law without exception."[411]  Fisher urges everyone to stop being complacent, to start becoming informed about vaccines and diseases and to act. Specifically, she states, "You are going to have to work to amend your state's laws. If you would like to be better informed and to help get the truth out, please join our grassroots vaccine safety movement."Holistic Health and Freedom of ChoiceFisher adds, "The alternative health care movement in this country is going to play a vital role in the vaccine safety movement.[412] Those who are looking into chiropractic, osteopathic medicine, naturopathic, homeopathic, vitamin therapy, etc., are looking for ways to boost the immune system through more natural means in order to be able to naturally deal with viruses and bacteria that they come in contact with. This is a very important movement."Dr. Dean Black, author of Immunizations: Compulsion or Choice, agrees. He sees vaccinations as only a shortcut for those people in our society who have not taken full responsibility for their health. "It's a way of saying, don't look at the more natural holistic way of helping the body. Medicine believes disease is the enemy....Medicine fights disease. Natural health care works with it...."Medicine believes symptoms are evil. Natural health care believes symptoms are the body's efforts to rid itself of disease."[413]Curtis Cost, author of Vaccines Are Dangerous: A Warning to the Black Community,adds, "We know through...studies that the incidences of various diseases have been declining steadily prior to the advent of various vaccines. We see declines up to 90 percent, and these declines result from improvements in sanitation and nutrition...."My point is that parents do not need to be terrified into believing that the only way to protect themselves and their children from disease is through vaccines. We know that if parents breastfeed their babies, the risk of death and disease is dramatically reduced because the breast milk contains all the natural nutrients that the mother will naturally give to her child as she breastfeeds. We know that diet has a tremendous effect on disease. If you are not eating a proper diet your risk of getting various diseases is much greater. So we need to focus on taking control of our health...to focus on eating more organically grown fresh fruits and vegetables, on drinking pure water, and on exercising. These actions build up the immune system."[414]Finally, the point is that individuals need the freedom to choose. They should not be forced in one direction or another. Barbara Loe Fisher stresses this: "Our organization does not tell a parent what to do.[415] I want to make that clear. We are an information clearinghouse and we believe in education. We believe that parents should take the responsibility for making their own decision. In this society, we ought to have the right to make the right decisions without being bullied and harassed and threatened into vaccinating if we do not believe that it is in the best interest of our child."Alan Phillips reminds us that we are kept in the dark about our freedom to choose. "Most states currently allow for medical and religious exemptions. You are not told this when you go to a pediatrician or when you enter a university. You are simply told that you have to vaccinate. But that is not usually true. Probably 15 to 20 states have a philosophical or personal exemption option that you don't even have to tie to your religion."I don't advocate that people do or do not vaccinate. I say that there's a lot of information that people should investigate before they make a decision one way or the other. We're so steeped in what I would now call the myth of vaccination that it seems nonsensical and counterintuitive to even raise the question. In fact, the first time that I raised the question with a pediatrician I got yelled at. While I think that was unprofessional of the pediatrician, it does demonstrate the degree to which assumptions about vaccinations are held."[416]Dr. Black states, "As a parent, there might be times I choose to immunize my child. Maybe I would find scientific evidence to back its validity in a case where a disease is so fraught with risk that I dare not expose my child. Maybe then I would choose [to vaccinate]. But I would do so having thoroughly thought about it....What I believe we cannot tolerate as a free nation is to have government bureaucrats come in and saybased upon false statistics-if you don't immunize your child, you will suffer penalty of law. That, to me, is a gross injustice that simply has to be changed."[417]It stands to reason, then, that our approach might be better directed to bolstering the effects of natural immunity, by strengthening the body's own disease fighting capability, rather than trying to manipulate a carefully balanced system which may or may not tip to the detriment of the future individual.  The old adage, 'What doesn't kill you makes you stronger', describes the credo of the vaccine industry.  The problem is that we do not yet know a single silver bullet remedy for all childhood illnesses, that are known to cause no harm to the future adult.To this argument, Trevor Gunn states, "for example, Vitamin A supplementation has been shown to reduce the mortality rate due to measles, in under 2 year olds, by seven times.  (From the British Medical Journal, 1987, p 294) "Many studies show increased eye problems and deaths in children with vitamin A deficiency."  In addition he cites the WHO's doctor Clements with regards to prevention of Cholera:  "the first line of defense should be providing safe clean water and proper waste disposal."The culmination of a review of a larger study that we mentioned earlier, which compared over 15,000 data sets for Union Army Soldiers over two distinct time periods (1830-1845) and (1918-1927), showed that length of life was improved in the 20th century, and in addition age of onset of chronic illness was also delayed.  The reviewer Robert Fogel noted that there  were two distinct explanations: The first, combining several outcomes, mentions reduction in debilitating chronic illness by eliminating causes of childhood illness, and the second, "increases in birth weight and adult frame size, which are likely the result of better nutrition, have been important in reducing mortality among infants and adults." (from the How the Aging Process Changed During the 20th Century, "Changes in the Process of Aging during the 20thCentury:  Findings and Procedures of the Early Indicators project)  ResourcesAdvisory Committee on Immunization PracticesCenters for Disease Control and PreventionNational Immunization ProgramDivision of Epidemiology and SurveillanceMail Stop E611600 Clifton Road, NEAtlanta, GA 30333Tel: 404-639-8096Web site: www.cdc.gov/nip/ACIP/default.htm    This is a pro-immunization site. To access the NIP's"Locating Information on Vaccine Safety"guide, go to www.cdc.gov/nip/vacsafe/research/resourceguide.htm.Association of American Physicians and Surgeons1601 N. Tucson Blvd., Suite 9Tucson, AZ 85716-3450Tel: 800-635-1196Web site: www.aapsonline.orgCitizens for Healthcare FreedomP.O. Box 62282Durham, NC 27715Web site: www.unc.edu/~aphillip/www/chf/index.htm    To read "Dispelling Vaccination Myths," by CHF director Alan Phillips, go to www.unc.edu/~aphillip/www/chf/myths/dvm1.htmConcerned Parents for Vaccine Safety8216 192nd St., Ct ESpanaway, WA 98387Web site: home.sprynet.com/~gyreneGary Null's Web SiteWeb site: www.garynull.comGlobal Vaccine Awareness League25422 Trabuco Road, Suite 105-230Lake Forest, CA 92630-2797Web site: www.gval.com"Homeopathic Disease Prevention"     This article by homeopathic practitioner Isaac Golden is availableat Homeopathy Online, a Journal of Homeopathic MedicineWeb site: www.lyghtforce.com/HomeopathyOnline/text/golden.htmImmunization Action Coalition1573 Selby AvenueSt. Paul, MN 55104Tel: 651-647-9009Web site: www.immunize.org   This is a pro-immunization site. For information on "State mandates on vaccination and vaccine-preventable disease," go to www.immunize.org/lawsInstitute for Vaccine SafetyBloomberg School of Public HealthJohns Hopkins University Web site: www.vaccinesafety.eduNational Network for Immunization Information66 Canal Center Plaza, Suite 600Alexandria, VA 22314Tel.: 877-341-6644Fax: 703-299-0204Web site: www.immunizationinfo.com    This is a pro-immunization site.National Vaccine Information Center 421-E Church St.Vienna, VA 22180Tel.: 1-800-909-SHOTFax: 703-938-5768  Web site: www.909shot.comParents Requesting Open Vaccine Education (PROVE)P.O. Box 91566Austin, TX 78709-1566Web site: www.vaccineinfo.netThe Phyllis Schlafly ReportP.O. Box 618Alton, IL 62002Tel.: 618-462-5415Web site: www.eagleforum.org/topics/vaccine/vaccine.html    This site contains a number of articles on vaccine topics.Thinktwice Global Vaccine InstituteP.O. Box 9638Santa Fe, NM 87504Web site: www.thinktwice.com    Also includes the Thijnktwice/New Atlantean Press bookstore,with a catalog of books on vaccination topicsVaccination Information Service     To order the video "Vaccination: The Hidden Truth."Web site: www.vaccination.inoz.com/default.htmlVaccination LiberationP.O. Box 1444Coeur d'Alene, Idaho 83816Tel.: 208-255-2307Web site: www.vaclib.orgVaccine Adverse Event Reporting System (VAERS)P.O. Box 1100Rockville, MD 20849-1100Tel: 800-822-7967Fax: 877-721-0366Web site: www.vaers.org   A more usable version of the VAERS data is available on a databasedeveloped by Steven Rubin. Go to www.nccn.net/~wwithin/vaers.htmVaccine Information and Awareness Web siteTel.: 858-484-3197Web site: www.access1.net/via    To access a list of pro-information groups, go to www.access1.net/via/PROCHOICE/prochoic.htm    To access state links, including information on state exemptions,go to www.access1.net/via/STATES/toc-states.htmVaccine resources by stateWeb site: http://proliberty.com/observer/vaclib/VACLIST.DOC"Vaccines: The Risks, the Benefits, the Choices"Doctor's Reference Manual (2001-02)Presented by Sherri J. Tenpenny, D.O.New Medical Awareness Seminars, LLC14761 Pearl Road #263Strongsville, OH 44136Tel: 440-572-1136Web site: www.osteomed.comVaccine Policy Institute251 W. Ridgeway DriveDayton, OH 45459Tel: 937-435-4750Web site: www.vaccinepolicy.orgVaccineWebsite.comWeb site: www.whale.to/vaccines.html"Alternative Approach to Disease" (video)By Gary Null"Building the Immune System Naturally" (video)By Gary NullThe Consumer's Guide to Childhood VaccinesBy Barbara Loe FisherNational Vaccine Information CenterImmunization Theory vs. Reality: Expos on VaccinationsBy Neil Z. MillerThe Atlantean Press, 1996Immunization: The Reality Behind the MythBy Walene JamesGreenwood Publishing Group, 2nd Edition, 1995Reverse the Aging Process NaturallyBy Gary Null and Martin Feldman, M.D.Villard Books, a division of Random House, 1993"Seven Steps to Perfect Health" (video)By Gary NullA Shot in the DarkBy Harris L. Coulter and Barbara Loe FisherAvery Publishing Group, 1991"Supercharge Your Immune System" (video)By Gary Null"Total Health" series, Steps 1 - 7 (videos)By Gary NullVaccination and Immunization: Dangers, Delusions & AlternativesBy Leon ChaitowBeekman Publishing, 1996Vaccines Are Dangerous: A Warning to the Black CommunityBy Curtis CostA & B Distributors & Publishers Group, 1992What Every Parent Should Know About Childhood ImmunizationBy Jamie MurphyEarth Healing Products, 1993Correspondence:Gary Null, PhDP.O. Box 918Planetarium StationNew York, New York 10024 USA646-505-4660/ Fax 212-472-5139e-mail: precisemd@aol.comReferences[1]  [1]Clin Infect Dis. 2006 Mar 1;42 Suppl 3:S141-4 A response to strategy #2: streamlining the regulatory process.Glezen WP. [2]Expert Rev Vaccines. 2003 Feb;2(1):15-9 Designing pediatric vaccine formularies and pricing pediatric combination vaccines using operations research models and algorithms. Jacobson SH, Sewell EC, [3] Clin Infect Dis. 2000 Jun;30 Suppl 3:S247-9 Moving new vaccines for tuberculosis through the regulatory process.Brennan MJ.   [4]MMWR Recomm Rep. 2006 Jul 28;55(RR-10):1-42 Prevention and Control of Influenza: recommendations of the Advisory Committee on Immunization Practices (ACIP).Advisory Committee on Immunization Practices; Smith NM,  [5] Vaccine. 2006 Apr 24;24(17):3530-7. Epub 2006 Feb 20 Stockpile levels for pediatric vaccines: how much is enough?Jacobson SH, Sewell EC, [6]Health Aff (Millwood). 2005 May-Jun;24(3):635-42 Factors affecting U.S. manufacturers' decisions to produce vaccines.Coleman MS, Sangrujee N,[7] MMWR Morb Mortal Wkly Rep. 2005 Apr 1;54(12):307-8 Influenza vaccine prebooking and distribution strategies for the 2005-06 influenza season. Centers for Disease Control and Prevention (CDC).   [8] MMWR Morb Mortal Wkly Rep. 2003 Jan 31;52(4):Q1-4. Recommended childhood and adolescent immunization schedule. United States, 2003. Centers for Disease Control and Prevention.Centers for Disease Control and Prevention (CDC).   [9] Public Health Rep. 2005 Sep-Oct;120(5):543-8 Enrollment of racial/ethnic minorities in NIAID-funded networks of HIV vaccine trials in the United States, 1988 to 2002.Djomand G, Katzman J, [10] Clin Infect Dis. 2005 Oct 15;41(8):1150-6. Epub 2005 Sep 2 Prospects for a group A streptococcal vaccine: rationale, feasibility, and obstacles--report of a National Institute of Allergy and Infectious Diseases workshop.Bisno AL, Rubin FA, [11]: Curr Opin Obstet Gynecol. 2006 Feb;18 Suppl 1:s15-21. Harnessing the power of prevention: human papillomavirus vaccines.Mayeaux EJ Jr.   [12]Obstet Gynecol Surv. 2006 Jun;61(6 Suppl 1):S26-31. Vaccines for the prevention of human papillomavirus and associated gynecologic diseases: a review.Ault KA.   [13]Obstet Gynecol Surv. 2006 Jun;61(6 Suppl 1):S26-31. Vaccines for the prevention of human papillomavirus and associated gynecologic diseases: a review.Ault KA.   [14]http://www.mayoclinic.com/health/vaccines/HQ01629[15]http://www.nber.org/digest/mar02/w8556.html[16]http://www.nber.org/digest/mar02/w8556.html[17]http://www.nber.org/digest/mar02/w8556.html[18]http://www.nber.org/digest/mar02/w8556.html[19]http://www.nber.org/digest/mar02/w8556.html[20]http://www.nber.org/digest/mar02/w8556.html[21]http://www.whale.to/m/gunn.html, p.7. [22]http://www.cdc.gov/nip/publications/fs/gen/WhatIfStop.htm[23] http: /www.nber.org/aginghealth/fall03/w9941.html [24]Circulation. 2003; 108:2957.) 2003 American Heart Association, Inc. Review: Current Perspective  Explaining How "High-Grade" Systemic Inflammation Accelerates Vascular Risk in Rheumatoid Arthritis  Naveed Sattar, MD; David W. McCarey [25] Lavrovsky, Y, Chattergee, B, role of Redox regulated transcription factors in inflammation, aging, and age related diseases, Experimental gerontology 35 (2000) 521-532 [26] New England Journal of medicine  Volume 352:1685-1695April 21, 2005 number 16Inflammation, Atherosclerosis, and Coronary Artery Disease  Gran K. Hansson, M.D., Ph.D. http://www.jacn.org/cgi/content/abstract/21/6/495[27] Coronary artery disease and rheumatoid arthritis. Epidemiology and health-related services Current Opinion in Rheumatology. 14(2):115-120, March 2002. Goodson, Nicola MRCP http://www.co-rheumatology.com/pt/re/corheum/abstract.00002281-200203000-00007.htm;jsessionid=FF5JM334D9JzKT6wQw2zS2HyRXQrVyF4G28v4P0vtmLGdLv2ln7S!1230047961!-949856144!8091!-1[28] Abuja, Peter M, Albertini, Riccardo, Methods for Monitoring oxidative stress, lipid peroxidation and oxidation resistance of lipoproteins, Clinica Chimica Acta 306 (2001) 1-17 [29]Biotechnology Journal Volume 1, Issue 4 , Pages 420 - 439Review: Essential fatty acids: biochemistry, physiology and pathology  [30] Pharmacological Reviews Vol. 52, Issue 4, 673-751, December 2000 The Effects of Plant Flavonoids on Mammalian Cells:Implications for Inflammation, Heart Disease, and Cancer Elliott Middleton, Jr. , Chithan Kandaswami [31]Experimental Biology and Medicine 231:1287-1299 (2006) 2006 Society for Experimental Biology and Medicine  MINIREVIEW Flavonoids Attenuate Cardiovascular Disease, Inhibit Phosphodiesterase, and Modulate Lipid Homeostasis in Adipose Tissue and Liver Michael R. Peluso1http://www.ebmonline.org/cgi/content/abstract/231/8/1287  [32]  2002 The American Society for Nutritional Sciences J. Nutr. 132:1825-1829, 2002 Biochemical and Molecular Actions of Nutrients Flavonoids of Cocoa Inhibit Recombinant Human 5-Lipoxygenase1Tankred Schewe, Hartmut Khn* and Helmut Sies23http://jn.nutrition.org/cgi/content/abstract/132/7/1825  [33] PNAS | January 24, 2006 | vol. 103 | no. 4 | 1024-1029 (-)-Epicatechin mediates beneficial effects of flavanol-rich cocoa on vascular function in humans  Hagen Schroeter *  , , Christian Heiss, http://www.pnas.org/cgi/content/abstract/103/4/1024[34] Clinical and Vaccine Immunology, March 2006, p. 319-328, Vol. 13, No. 3 doi:10.1128/CVI.13.3.319-328.2006Copyright  2006, American Society for Microbiology. All Rights Reserved. The Flavonoid Quercetin Inhibits Proinflammatory Cytokine (Tumor Necrosis Factor Alpha) Gene Expression in Normal Peripheral Blood Mononuclear Cells via Modulation of the NF-  System Madhavan P. Nair,* Supriya Mahajan, http://cvi.asm.org/cgi/content/abstract/13/3/319[35]  2005 The American Society for Nutritional Sciences J. Nutr. 135:172-178, February 2005 Biochemical and Molecular Actions of Nutrients The Flavonoid Phloretin Suppresses Stimulated Expression of Endothelial Adhesion Molecules and Reduces Activation of Human Platelets Verena Stangl*,1, Mario Lorenz http://jn.nutrition.org/cgi/content/abstract/135/2/172*,[36] American Journal of Clinical Nutrition, Vol. 78, No. 3, 570S-578S, September 2003  2003 American Society for Clinical Nutrition Fruits and vegetables in the prevention of cellular oxidative damage1,2,3,4,5Ronald L Prior http://www.ajcn.org/cgi/content/abstract/78/3/570S[37] (Arteriosclerosis, Thrombosis, and Vascular Biology. 2001;21:1084.) 2001 American Heart Association, Inc. Effect of Acute and Chronic Tea Consumption on Platelet Aggregation in Patients With Coronary Artery Disease Stephen J. Duffy; Joseph A. Vita [38] Journal of the American College of Nutrition, Vol. 21, No. 6, 495-505 (2002) Published by the American College of Nutrition Omega-3 Fatty Acids in Inflammation and Autoimmune Diseases Artemis P. Simopoulos, MD, FACN The Center for Genetics, Nutrition and Health, Washington, D.C[39] American Journal of Clinical Nutrition, Vol. 76, No. 3, 560-568, September 2002  2002 American Society for Clinical Nutrition Flavonoid intake and risk of chronic diseases1,2Paul Knekt, Jorma Kumpulainenhttp://www.ajcn.org/cgi/content/abstract/76/3/560[40]Relationship Between Physical Activity and Inflammation Among Apparently Healthy Middle-aged and Older US Adults Jerome L. Abramson, PhD; Viola Vaccarino, MD, PhD  Arch Intern Med. 2002;162:1286-1292. http://archinte.ama-assn.org/cgi/content/abstract/162/11/1286[41] American Journal of Clinical Nutrition, Vol. 70, No. 3, 532S-538S, September 1999  1999 American Society for Clinical Nutrition Associations between diet and cancer, ischemic heart disease, and all-cause mortality in non-Hispanic white California Seventh-day Adventists1,2,3  Gary E Fraser http://intl.ajcn.org/cgi/content/abstract/70/3/532S  [42] Medical careJanuary 1999, 37:1 >  Evidence Suggesting That a Chronic Disease Self-Management Program Can Improve Health Status While Reducing Hospitalization: A Randomized Trial. http://www.lwwmedicalcare.com/pt/re/medcare/abstract.00005650-199901000-00003.htm;jsessionid=FF8ZLxQTfJhFFMrFJBys0Tc7Rb6GmSGLSLQ2sLlrbJ5rJ3YR1lpk!-210589086!-949856145!8091!-1[43]Wei Young, Robert L. Hotovec, and Arthur G. Romero, "Tea and Atherosclerosis", Nature, December 9, 1967, Vol. 216, Num. 0, pp. 1015-1016 http://www.healthsentinel.com/briefs.php?id=035&title=Coffee&event=briefs_print_list_item[44] http: /www.nber.org/aginghealth/fall03/w9941.html p.2. [45] http: /www.nber.org/aginghealth/fall03/w9941.html p.2. [46] http: /www.nber.org/aginghealth/fall03/w9941.html p.2. [47]http://www.vaclib.org/intro/present/index.htm#8, Vaccination, a parent's Dilemma [48] United States mortality rate from measles, scarlet fever, typhoid, whooping cough, and diphtheria, http://www.healthsentinel.com/graphs.php?id=14&event=graphs_print_list_item[49]http://www.healthsentinel.com/graphs.php?id=14&event=graphs_print_list_item[50] http: /www.nber.org/aginghealth/fall03/w9941.html p.2. [51]Vaccine Safety Vaccines: A Safe Choice Vaccine Safety Information for Parents http://www.cdc.gov/nip/vacsafe/vacsafe-parents.htm[52]http://www.iahf.com/20020702.htmlUK babies given toxic vaccines, admits GlaxoAntony Barnett and Tracy McVeigh Sunday June 30, 2002 The Observerhttp://www.observer.co.uk/uk_news/story/0,6903,746568,00.html[53]http://www.fda.gov/opacom/factsheets/justthefacts/19vaccine.html Vaccines Provide Effective Protection and FDA Makes Sure They are Safe [54]http://www.eagleforum.org/educate/1998/nov98/vaccinations.htmlCompulsory Vaccinations Put American Children at Risk[55]http://www.k12.dc.us/dcps/policies/policies_intro.html#immunization Immunization Requirements[56]http://www.cispimmunize.org/IZSchedule_2006.pdf-  -immunization chart   [57]http://www.npr.org/templates/story/story.php?storyId=4585992&sourceCode=RSSSalk Polio Vaccine Conquered Terrifying Disease Source: Global Polio Eradication Initiative U.S. Centers for Disease Control and Prevention; the University of Michigan; PBS Online[58] Polio Vaccine: It Tamed a Scourge, Transformed Medicine Related Health News By Amanda GardnerHealthDay Reporter TUESDAY, April 12 (HealthDay News) Nancy Green, M.D., medical director, March of Dimes, White Plains, N.Y.; David Rose, archivist, March of Dimes, White Plains, N.Y. [59]http://www.unicef.org/media/media_18979.html Information note 2004 - Now More than Ever: End Polio Forever[60]http://www.fda.gov/Cber/vaers/articles.htmVaccine Adverse Event Report System (VAERS):DocumentsFEDERAL REGISTER: Vaccine Adverse Event Reporting; Revised Form VAERS-2; Withdrawal of Proposed Revised Form - 4/21/2006 - (PDF), (Text)         Federal Register Notice; Vaccine Adverse Event Reporting System; Revised Form VAERS-2; Availability - 11/20/2001 - (PDF), (Text)           Draft Form (for comment) - (PDF), Instructions - (PDF)  Guidance for Industry: How to Complete the Vaccine Adverse Event Reporting System Form (VAERS-1) - 9/8/1998 (PDF), (Text)Dear Colleague Letter: Use of Haemophilus influenzae Vaccines in Combination with DTaP in Infants - 8/12/1998 VAERS Bibliography: CDC/FDA PublicationsConsumer Articles  1.      How the FDA works to Ensure Vaccine Safety FDA Consumer December 1995  2. Adults Need Tetanus Shots, Too FDA Consumer July-August 1996  3. First Vaccine for Chickenpox FDA Consumer September 1995  4. Vaccine Safety Crucial but Impossible to Guarantee. Infectious Diseases in Children, 1996;9(1):33-35.  5.      Physicians play a pivotal role in vaccine safety. AAP News, Feb., 1996.  Professional Articles  1.      Ball LK, Ball R, Pratt RD. Assessment of thimerosal use in childhood vaccines. Pediatrics 2001;107:1147-1154.  2.      Ball R, Ball LK, Wise R, Braun MM, Beeler JA, Salive M. Stevens Johnson syndrome and toxic epidermal necrolysis after vaccination: Reports to the Vaccine Adverse Event Reporting System. Pediatric Infectious Disease Journal 2001;20:219-223.  3.      Ball R, Braun MM, Mootrey GT. Safety data on meningococcal polysaccharide vaccine from the Vaccine Adverse Event Reporting System. Clinical Infectious Diseases 2001;32:1273-1280.  4.      Beeler J, Varricchio F, Wise RP. Thrombocytopenia after immunization with measles vaccines: Review of the Vaccine Adverse Events Reporting System (1990 to 1994). The Pediatric Infectious Disease Journal. 1996;15:1,88-90.  5.      Braun MM, Ellenberg SS. Descriptive epidemiology of adverse events following immunization: reports to the Vaccine Adverse Events Reporting System (VAERS), 1991-1994. Journal of Pediatrics 1997; 131:529-35.  6.      Braun MM, Mootrey GT, Salive ME, Chen RT, Ellenberg SS, and the VAERS Working Group. Infant immunization with acellular pertussis vaccines in the US: Assessment of the first two years' data from the Vaccine Adverse Event Reporting System (VAERS). Pediatrics electronic pages 2000;106:e51 and Pediatrics 2000;106:821.  7.      Braun MM, Patriarca PA, Ellenberg SS. Syncope after immunization. Archives of Pediatrics and Adolescent Medicine. 151:255-9; 1997.  8.      Braun MM, Terracciano G, Salive ME, Blumberg DA, Vermeer-de Bondt PE, Heijbel H, Evans G, Patriarca PA, Ellenberg SS. Report of a US Public Health Service Workshop on Hypotonic-Hyporesponsive Episode (HHE) Following Pertussis Immunization. Pediatrics electronic pages 1998;102:e52 and Pediatrics 1998;102:1201-2.  9.      Centers for Disease Control and Prevention. Vaccine Adverse Event Reporting System-United States. MMWR Morbidity and Mortality Weekly Report, 1990; 39(RR-41):730-33.  10.  Chen RT, Glasser JW, Rhodes PH, Wise RP, et. al. Vaccine Safety Datalink Project: A new tool for improving vaccine safety monitoring in the United States. Pediatrics. 99(6):765-73;1997.  11.  Chen RT, Rastogi SC, Mullen JR et. al. The Vaccine Adverse Event Reporting System (VAERS). Vaccine. 1994;12:542-50.  12.  Chen RT, Phillips L, Hadler S. Bottom Line: Vaccination benefits far outweigh risks [letter]. The Nations Health, Dec. 1995;2.  13.  Clements, CJ, Ball, LK, Ball, R. Ball, Pratt, RD. Thiomersal in vaccines (letter). Lancet, 2000; 355:1279-1280.  14.  Commentary. CDC Officials help physicians answer DTP-safety questions. American Academy of Pediatrics News, 1995; 11(3):9-11.  15.  DuVernoy TS, Braun MM. Hypotonic Hyporesponsive Episodes Reported to the Vaccine Adverse Event Reporting System (VAERS), 1996-1998. Pediatrics electronic pages 2000;106:e52 and Pediatrics 2000;106:821-2.  16.  Ellenberg SS, Chen RT, The complicated task of monitoring vaccine safety. Public Health Reports, 112:10-20, 1997.  17.  Howson, et al. Adverse Effects of Pertussis and Rubella Vaccines. Washington, DC: National Academy Press, 1991.  18.  Niu MT, Davis, DM, and Ellenberg SS. Recombinant hepatitis B vaccination of neonates and infants: Emerging safety data from the Vaccine Adverse Event Reporting System. Pediatric Infectious Disease Journal, 1996;15:771-76.  19.  Niu MT, Rhodes P, Salive ME, Lively T, Davis DM, et. al. Comparative safety of two recombinant hepatitis B vaccines in children: data from the Vaccine Adverse Event Reporting System (VAERS) and Vaccine Safety Datalink (VSD). Journal of Clinical Epidemiology, 1998; Vol 51, 6:503-510.  20.  Niu MT, Salive ME, Krueger CL, Ellenberg SS. Two year review of hepatitis A vaccine safety: Data from the Vaccine Adverse Event Reporting System (VAERS). Clinical Infectious Disease 1998;26:1475-6.  21.  Niu MT, Salive ME, Ellenberg SS. Post-marketing surveillance for adverse events after vaccination: The national Vaccine Adverse Event Reporting System (VAERS), MEDWATCH CME credit article (FDA/CBER publication), November, 1998.  22.  Niu MT, Salive ME, Ellenberg SS. Reporting adverse events after vaccination: The national Vaccine Adverse Event Reporting System (VAERS) Federal Practitioner 1998; 15; 13-21,37.  23.  Niu MT, Salive ME, Ellenberg SS. Neonatal deaths after hepatitis B vaccine, VAERS, 1991-1998. Arch Pediatr Adoles Med 1999; 153:1279-82.  24.  Rosenthal S, Chen RT. The reporting sensitivities of two passive surveillance systems for Vaccine Adverse Events. American Journal of Public Health, 1995; 85(12):1706-09.  25.  Singleton JA, Loyd, JL, Mootrey, GT, Salive, ME, Chen, RT. An overview of the Vaccine Adverse Event Reporting System (VAERS) as a surveillance system. Vaccine 1999;17(22):2908-17.  26.  Stratton, et al. Adverse Events Associated with Childhood Vaccines, Evidence Bearing on Causality. Washington, DC: National Academy Press, 1993.  27.  Varricchio, F. The vaccine adverse event reporting system. Clinical Toxicology, 36(7), 765-68 (1998).  28.  Wise RP, Kiminyo KP, Salive ME. Hair loss following routine immunizations. Journal of the American Medical Association. 1997; 278:1176-8.  29.  Wise RP, Salive ME, Braun MM, Mootrey GT, Seward JF, Rider LG, Krause PR, Postlicensure safety surveillance for varicella vaccine, Journal of the American Medical Association, September 13, 2000, 284(10):1271-9.           Supplementary references  Zanardi LR, Haber P, Mootrey GT, Niu, MT, Wharton M. Intussusception among recipients of rotavirus vaccine--reports to the Vaccine Adverse Event Reporting System, 2001; Pediatrics , in press.  [61] June Russell's Health FactsVaccinations http://www.jrussellshealth.com/immune.html{"Fitness On Line" - Nov. 1999 Natural Health magazine}{"Vaccination: Prevention or Poison?" Delicious magazine, Sept. 1994, by Kathleen Finn} {"Vaccinations - Deception and Tragedy" - Michael Dye} Health Freedom News - May 1984. "How Do The Vaccines Work?" Richard Moskowitz, MD}{"Supporting Children's Health" - Philip Incao, MD, Alternative Medicine Digest, Aug./Sept. 1997} According to an article in The Lancet (1985), "Measles Virus Infection Without Rash in Childhood is Related to Disease in Adult Life," Leon Chaitow in his book, "Vaccinations and Vaccinations: Dangers Delusions and Alternatives,"   [62] Vaccination Debate: Do Vaccines Cause Cot Deaths? Harris L. Coulter, PhD, http://www.pnc.com.au/~cafmr/coulter/vacc-deb.html  [63] Virchows Arch. 2006 Jan;448(1):100-4. Epub 2005 Oct 18. Sudden infant death syndrome (SIDS) shortly after hexavalent vaccination: another pathology in suspected SIDS? Ottaviani G, Lavezzi AM, [64] National Academy of sciences Press Relaease Date: March 12, 2003  http://www.cdc.gov/nip/publications/#Diseaseshadalready 'SIDS Not Linked to Number and Variety of Childhood Vaccines', says IOM[65]http://www.fda.gov/fdac/features/2001/401_vacc.htmlU.S. Food and Drug AdministrationFDA Consumer magazineJuly-August 2001 Understanding Vaccine Safety: Immunization Remains Our Best Defense Against Deadly Disease 'Alleged Associations' [66]http://www.fda.gov/fdac/features/095_vacc.html Developing New Pertussis Vaccines[67] Am J Prev Med. 2002 Apr;22(3):170-6. Pediatric deaths reported after vaccination: the utility of information obtained from parents.Silvers LE, Varricchio FE, [68] Pharmacoepidemiol Drug Saf. 2001 Jun-Jul;10(4):279-85. The epidemiology of fatalities reported to the vaccine adverse event reporting system 1990-1997.Silvers LE, Ellenberg SS, [69]J Paediatr Child Health. 2003 Sep-Oct;39(7):487-91 Immunization myths and realities: responding to arguments against immunization.MacIntyre CR, Leask J. Children's Hospital at Westmead, Westmead and University of Sydney, Sydney, New South Wales, Australia. RainaM@chw.edu.au  [70] Vaccine. 2006 Aug 4; Sudden infant death syndrome: No increased risk after immunisation. Vennemann MM, Butterfass-Bahloul T, [71]http://www.answers.com/topic/cigarette cigarette [72]http://www.upenn.edu/pnc/ptverkuil.html "A Leadership Case Study of Tobacco and its Regulation" Paul Verkuil Benjamin N. Cardozo School of Law [73]http://www.brownandcrouppen.com/news.html Lawsuit Charges HRT Caused Breast Cancer and Debilitating Stroke [74]http://www.medicalnewstoday.com/medicalnews.php?newsid=50004Hormone Replacement Therapy Study Good News For Some POSTED: 5:43 p.m. PDT August 26, 2003[75] http://www.chron.com/disp/story.mpl/ap/fn/4178876.html  Sept. 11, 2006, 5:48PMLawyers Say Wyeth Drugs Promoted Cancer By ANDREW DeMILLO Associated Press Writer  2006 TheAssociated Press[76] Hormone replacement therapy (HRT) http://www.nlm.nih.gov/medlineplus/ency/article/007111.htm[77]Hormone replacement therapy (HRT) http://www.nlm.nih.gov/medlineplus/ency/article/007111.htm  [78]http://www.brownandcrouppen.com/news.htmlNIH Sends 11,000 Letters to Estrogen-Alone Study ParticipantsThe National Institutes of Health (NIH) has advised participants in the Women's Health Initiative (WHI) to stop taking their estrogen-alone study pills due to stroke risk and other findings in otherwise healthy women.[79]http://www.ahrp.org/infomail/04/10/12.php Pre 2006 Archives of the Alliance for Human Research Protection How Did the Vioxx Debacle Happen? USA Today / Lancet Tue, 12 Oct 2004 [80]http://www.flexicose.com/flexicose/COX-2-Death.htmlCox-II Inhibitors - Why They "Work" and Also Why They Can Potentially be Fatal[81]First of four parts http://www.dailypress.com/news/dp-anthday1dec02,0,7450119.story?coll=dp-widget-newsAn Incomplete Picture Despite promises that hospitalizations after anthrax vaccinations would be reported, the Pentagon withheld data on more than 20,000 cases.  BY BOB EVANS December 4, 2005[82]http://www.vaccinationnews.com/Adverse_Reactions/VAERS/credible_estimates.htmJames Froeschle, Connaught Laboratories, Swiftwater, Pennsylvania [83]http://medicine.plosjournals.org/perlserv/?request=advancedsearch&row_start=1&limit=10&order=score&search_fulltext=1&issn=1549-1676&jrn_issn=1549-1676&anywhere_type=any&anywhere=Frequency+of+Adverse+Events+after+Vaccination+with+Different+Vaccinia+&x=15&y=16 Frequency of Adverse Events after Vaccination with Different Vaccinia Strains Mirjam Kretzschmar1,2*, Jacco Wallinga1[84]http://www.vaccinationnews.com/Adverse_Reactions/VAERS/credible_estimates.htmJamesDavid Kessler statement in JAMA - June 2, 1993,vol.269, No.21, p.2785[85] Murphy, Jamie. What Every Parent Should Know About Childhood Immunization, Earth Healing Products, Boston, 1993. http://www.amazon.com/Every-Parent-Should-Childhood-Immunization/dp/0963037307/sr=1-14/qid=1158257640/ref=sr_1_14/102-3250943-7888120?ie=UTF8&s=books[86]http://darwin.nap.edu/books/0309057914/html/29.html Research to Identify Risks for Adverse Events Following Vaccination: Biological Mechanisms and Possible Means of Prevention Cynthia J. Howe, Richard B. Johnston, and E. Russell Alexander, EditorNational Academies Press[87]http://www.dailycamera.com/bdc/broomfield_home_life/article/0,1713,BDC_11938_4928345,00.html Shots all around As school gets under way, so should children's immunization By Terri Chance, Enterprise Staff Writer August 19, 2006[88]http://wmc.who.int/pdf/Vaccine_Adverse_Events_in_the_New_Mill.pdf#search=%22age%20vaccination%20adverse%20events%22Vaccine adverse events in the new millennium: is there reason for ...concern?  BJ Ward p.208 [89]http://www.immregistries.org/news/advocacy.phtmlADVOCACYAIRA is proud to be a member of the 317 Coalition (http://www.317coalition.org). Formed in April 2006, the sole focus of the coalition is advocating for increased 317 funds. Update on FY 2007 Labor HHS Appropriations Bill CDC Immunization Funding (Section 317) [90]http://www.hhs.gov/news/speech/2003/030320.html TOMMY G. THOMPSON, SECRETARY OF HEALTH AND HUMAN  SERVICES Before the House Appropriations Subcommittee on Labor, HHS, Education March 20, 2003 p.2,[91] Braun MM, et al. Descriptive epidemiology of adverse events after immunization: reports to the Vaccine Adverse Event Reporting System (VAERS), 1991-1994. J Pediatr 1997 Oct; 131(4):529-35.[92]http://www.vaccinationnews.com/Adverse_Reactions/VAERS/credible_estimates.htmConnaught testimony to the Institute of Medicine[93] The anthrax vaccine: New questions, weak data  Posted on Fri, Dec. 09, 2005 http://www.charlotte.com/mld/charlotte/news/nation/13368280.htm  The anthrax vaccine: New questions, weak data Over 20,000 troops hospitalized from anthrax vaccine Sun, Dec 11 2005 10:02 pm[94]http://whale.to/vaccines/studies.html Vaccine long term studies[95]http://www.vaccinesafety.edu/mmrandibd.htm The following Research Letter appeared in The Lancet Vol 351 - May 2, 1998. pg 1327-8. No evidence for measles, mumps, and rubella vaccineassociated inflammatory bowel disease or autism in a 14-year prospective study[96]http://www.cfah.org/hbns/getDocument.cfm?documentID=1154  Release Date:October 18, 2005, 7:01 PM US Eastern time Newest Study Finds No Link Between MMR Vaccine and AutismBy Laura Kennedy, Contributing Writer  Health Behavior News Service[97]http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=16235361&dopt=AbstractCochrane Database Syst Rev. 2005 Oct 19;(4):CD004407.Vaccines for measles, mumps and rubella in children.Demicheli V, Jefferson T, Rivetti A, Price D.[98]http://www.vaccines.bizland.com/lkj.htmFact #1: Approximately 1/3 of Doctors Refuse Vaccinations, yet . . [99] JAMA. 1981 Feb 20;245(7):711-3. Rubella vaccine and susceptible hospital employees. Poor physician participation. Orenstein WA, Heseltine PN, [100]Mendelsohn, Dr. Robert, "The Drive to Immunize Adults," Herald of Holistic Health Newsletter, Sept.-Oct. 1985. Yih WK, Lieu TA, [101] Orenstein WA, Heseltine PN, LeGagnoux SJ, Portnoy B. Rubella vaccine and susceptible hospital employees. Poor physician participation. JAMA 1981 Feb 20; 245(7):711-3.[102]http://occmed.oxfordjournals.org/cgi/reprint/54/4/231.pdf#search=%22Attitudes%20of%20general%20practitioners%20towards%20their%20vaccination%20against%20hepatitis%20B.%22:  Management of hepatitis B immunizations and blood exposure incidents in primary care  Occupational medicine 2004; 54:  231-237  DOI: 10.1093/occmed/kgh 037   [103] Kinnersley P. Attitudes of general practitioners towards their vaccination against hepatitis B. BMJ 1990 Jan 27; 300(6719):238.[104]http://occmed.oxfordjournals.org/cgi/reprint/54/4/231.pdf#search=%22Attitudes%20of%20general%20practitioners%20towards%20their%20vaccination%20against%20hepatitis%20B.%22:  Management of hepatitis B immunizations and blood exposure incidents in primary care  Occupational medicine 2004; 54:  231-237  DOI: 10.1093/occmed/kgh 037  [105] Gary Null Interview with Jamie Murphy, December 18, 1997.[106] James, Walene. Immunization: The Reality Behind the Myth, Bergin & Gervey, Massachusetts, 1988. [107] Gary Null Interview with Walene James, April 6, 1995.[108] Gary Null Interview with Jamie Murphy, December 18, 1997.[109] Phillips, Alan. Vaccination: dispelling the myths. Nexus, October-November 1997.[110] J Infect Dis. 1994 Jan;169(1):77-82.Sustained transmission of mumps in a highly vaccinated population: assessment of primary vaccine failure and waning vaccine-induced immunity.Briss PA, Fehrs LJ,  [111] Ibid.[112] Clin Immunol Immunopathol. 1996 May;79(2):163-70 Changes within T cell receptor V beta subsets in infants following measles vaccination. Auwaerter PG, Hussey GD, [113] Auwaerter PG, Hussey GD, Goddard EA, Hughes J, et al. Changes within T cell receptor V beta subsets in infants following measles vaccination. Clin Immunol Immunopathol 1996 May; 79(2):163-70.110 J Infect Dis. 1994 Jan;169(1):77-82. Sustained transmission of mumps in a highly vaccinated population: assessment of primary vaccine failure and waning vaccine-induced immunity.Briss PA, Fehrs LJ, Parker RA114Clin Immunol Immunopathol. 1996 May;79(2):163-70 Changes within T cell receptor V beta subsets in infants following measles vaccination.Auwaerter PG, Hussey GD, 113Auwaerter PG, Hussey GD, Goddard EA, Hughes J, et al. Changes within T cell receptor V beta subsets in infants following measles vaccination. Clin Immunol Immunopathol 1996 May; 79(2):163-70.  [114] Morbidity and Mortality Weekly Report Centers for Disease Control and Prevention1600 Clifton Rd, MailStop K-95, Atlanta, GA 30333, U.S.A  Department of Healthand Human ServicesThis page last reviewed 5/2/01 Recommendations and Reports  July 12, 1996 / 45(RR11);1-25 Prevention of Varicella: Recommendations of the Advisory Committee on Immunization Practices (ACIP) Summary [115] Am J Perinatol. 2003 Aug;20(6):321-32. A population-based study of the effects of birth weight on early developmental delay ordisability in children.Thompson JR, Carter RL,    [116] Natl Vital Stat Rep. 2003 Jun 25;51(11):1-20.  Links  Births: preliminary data for 2002.Hamilton BE, Martin JA, Sutton PD; U.S. Department of Health and Human Services Centers for Disease Control and Prevention. [117] Scholl, T., et al. Dietary and serum folate: their influence on the outcome of pregnancy. American Journal of Clinical Nutrition, volume 63, April 1996, pages 520-525.    [118]http://www.marchofdimes.com/professionals/681_1153.asp114 Morbidity and Mortality Weekly Report Centers for Disease Control and Prevention1600 Clifton Rd, MailStop K-95, Atlanta, GA 30333, U.S.A  Department of Healthand Human ServicesThis page last reviewed 5/2/01 Recommendations and Reports  July 12, 1996 / 45(RR11);1-25 Prevention of Varicella: Recommendations of the Advisory Committee on Immunization Practices (ACIP) Summary [120] Morbidity and Mortality Weekly Report Centers for Disease Control and Prevention1600 Clifton Rd, MailStop K-95, Atlanta, GA 30333, U.S.A  Department of Healthand Human ServicesThis page last reviewed 5/2/01 Recommendations and Reports  July 12, 1996 / 45(RR11);1-25 Prevention of Varicella: Recommendations of the Advisory Committee on Immunization Practices (ACIP) Summary [121] Morbidity and Mortality Weekly Report Centers for Disease Control and Prevention1600 Clifton Rd, MailStop K-95, Atlanta, GA 30333, U.S.A  Department of Healthand Human ServicesThis page last reviewed 5/2/01 Recommendations and Reports  July 12, 1996 / 45(RR11);1-25 Prevention of Varicella: Recommendations of the Advisory Committee on Immunization Practices (ACIP) Summary [122] Morbidity and Mortality Weekly Report Centers for Disease Control and Prevention1600 Clifton Rd, MailStop K-95, Atlanta, GA 30333, U.S.A  Department of Healthand Human ServicesThis page last reviewed 5/2/01 Recommendations and Reports  July 12, 1996 / 45(RR11);1-25 Prevention of Varicella: Recommendations of the Advisory Committee on Immunization Practices (ACIP) Summary [123] Gary Null interview with Dr. Dean Black, April 7, 1995.[124] Cournoyer, op. cit., p. 150-1.[125] Miller, Neil Z. Vaccines: Are They Really Safe and Effective? A Parent's Guide to Childhood Shots, New Atlantean Press, Santa Fe, NM, 1992, p. 46.[126] Lovett, Lisa, et al. Immunity, Why Not Keep It? Technical Publications, Victoria, Australia.[127] Yves De Latte. Vaccinations: The Untold Truth, AUM Publications, San Antonio, TX, 1990, p. 65.[128] Miller NZ, op. cit.[129] Hearings Before the Committee on Interstate and Foreign Commerce, House of Representatives, 87th Congress, Second Session on H.R. 10541, May 1962, p. 94.[130] Coulter, Harris L and Fisher, Barbara Loe. A Shot in the Dark, Avery Publishing Group, Garden City Park, NY, 1991. [131] Coulter, Harris L. Vaccination, Social Violence, and Criminality, North Atlantic Books, Berkeley, CA, 1990. [132] Gary Null Interview with Dr. Harris Coulter, April 6, 1995.[133]Australian Nurses Journal, June 1981.[134] Gary Null Interview with Alan Phillips, December 17, 1997.[135] Gary Null Interview with Steven Lanka, [136] Phillips, op. cit.[137] Gary Null Interview with Walene James, April 6, 1995.[138] Merck & Co., Inc. Prescribing information for Recombivax HB Hepatitis B Vaccine (Recombinant). Issued August 2002.[139] SmithKline Beecham Pharmaceuticals. Prescribing information for Engerix-B Hepatitis B Vaccine (Recombinant). Date of issuance November 2001.[140] Merck & Co., op. cit.[141] Aventis Pasteur Inc. Prescribing information for Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Absorbed, Tripedia. Product information as of September 2000.[142] SmithKline Beecham Pharmaceuticals. Prescribing information for Infanrix Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Absorbed. Date of issuance December 2001.[143] Aventis Pasteur Inc. Prescribing information for Poliovirus Vaccine Inactivated, IPOL. Product information as of December 1999.[144] Merck & Co., Inc. Prescribing information for M-M-R II (Measles, Mumps, and Rubella Virus Vaccine Live). Issued August 2001.[145] Merck & Co., Inc. Prescribing information for Varivax [Varicella Virus Vaccine Live (Oka/Merck)]. Issued November 2000.[146] Phillips, op. cit.[147] Murphy, op. cit., p. 5.[148] Thimerosal in Vaccines: A Joint Statement of the American Academy of Pediatrics and the Public Health Service. MMWR07/09/1999; 48(26):563. [149] Thimerosal and vaccines: an Institute of Medicine (IOM) report. Centers for Disease Control and Prevention, National Immunization Program, Atlanta, GA. From http://www.cdc.gov/nip/vacsafe/concerns/thimerosal/iomthim10-1-01.htm Last modified October 24, 2001.[150] Thimerosal in vaccines: frequently asked questions. Food and Drug Administration. From www.fda.gov/cber/vaccine/thimfaq.htm. Last updated October 5, 2001.[151] Ibid.[152] Sakamoto M, et al.Widespread neuronal degeneration in rats following oral administration of methylmercury during the postnataldeveloping phase: a model of fetal-type minamata disease. Brain Res 1998 Feb 16; 784(1-2):351-4. [153] Echeverria D, et al. Neurobehavioral effects from exposure to dental amalgam Hg(o): new distinctions between recent exposure and Hg body burden. FASEB J 1998 Aug; 12(11):971-80. [154] Myers GJ, et al. A review of methylmercury and child development. Neurotoxicology 1998 Apr; 19(2):313-28. [155] Myers GJ, et al. Prenatal methylmercury exposure and children: neurologic, developmental, and behavioral research. Environ Health Perspect 1998 Jun; 106 Suppl 3:841-7. [156] Thimerosal in vaccines: frequently asked questions, op cit.[157] Immunization update 2002: influenza vaccine. Centers for Disease Control and Prevention, Atlanta, GA. Satellite broadcast, August 15, 2002. From http://www.cdc.gov/flu/professionals/bulletin/2002-03/bulletin4_091302.htm[158] FDA approves preservative-free influenza vaccine for pediatric use. Press release. Aventis Pasteur. September 12, 2002.[159]http://www.cdc.gov/nip/vaccine/vacc-timeline.htm[160]http://www.cdc.gov/nip/vaccine/vacc-timeline.htm[161]http://www.pdhealth.mil/deployments/gulfwar/enviro_anthrax_vac.asp[162] Phillips, op. cit.[163] Measles vaccine failures: lack of sustained measles specific immunoglobulin G responses in revaccinated adolescents and young adults. Pediatr Infect Dis J 1994 Jan; 13(1):34-8. [164] Measles outbreak in 31 schools: risk factors for vaccine failure and evaluation of a selective revaccination strategy. Can Med Assoc J 1994 Apr 1; 150(7):1093-8. [165] Haemophilus b disease after vaccination with haemophilus b polysaccharide or conjugate vaccine. Am J Dis Child 1991 Dec; 145(12):1379-82.[166] Sustained transmission of mumps in a highly vaccinated population: assessment of primary vaccine failure and waning vaccine-induced immunity. J Infect Dis 1994 Jan 1; 169(1):77-82.[167] Secondary measles vaccine failure in healthcare workers exposed to infected patients. Infect Control Hosp Epidemiol 1993 Feb; 14(2):81-6.[168] Failure to reach the goal of measles elimination. apparent paradox of measles infections in immunized persons. Arch Intern Med 1994 Aug 22; 154(16):1815-20. [169] Auwaerter, op. cit. [170] Outbreak of paralytic poliomyelitis in oman; evidence for widespread transmission among fully vaccinated children. Lancet 1991 Sep 21; 338:715-20.47http://www.vaclib.org/intro/present/index.htm#8, Vaccination, a parent's Dilemma 48 United States mortality rate from measles, scarlet fever, typhoid, whooping cough, and diphtheria, http://www.healthsentinel.com/graphs.php?id=14&event=graphs_print_list_item49http://www.healthsentinel.com/graphs.php?id=14&event=graphs_print_list_item50http://www.nber.org/aginghealth/fall03/w9941.html[171] Sato H, et al. Experience with diphtheria toxoid-tetanus toxoid-acellular pertussis vaccine in Japan. Clin Infect Dis 1999 Jun; 28 Suppl 2:S124-30. [172] Williams, AL. News and perspectives: new vaccines for childhood immunization. Drug Benefit Trends 1997; 9(3):10-11,15-22. [173] Rosenthal S, Chen R, Hadler S. The safety of acellular pertussis vaccine vs whole-cell pertussis vaccine. A postmarketing assessment. Arch Pediatr Adolesc Med 1996 May; 150(5):457-60. [174] Halperin SA, et al. Persistence of pertussis in an immunized population: results of the Nova Scotia Enhanced Pertussis Surveillance Program. J Pediatr 1989 Nov; 115(5 Pt 1):686-93. [175] de Melker, HE., et al. Pertussis in the Netherlands: an outbreak despite high levels of immunization with whole-cell vaccine. Emerging Infectious Diseases 1997; 3(2):175-8. Centers for Disease Control. [176] Hutchins SS, et al. Current epidemiology of pertussis in the United States. Tokai J Exp Clin Med 1988; 13 Suppl:103-9. [177] Ranganathan S, et al. Pertussis is increasing in unimmunized infants: is a change in policy needed? Arch Dis Child 1999 Mar; 80(3):297-9. [178] Williams GD, et al. Infant pertussis deaths in New South Wales 1996-1997. Med J Aust 1998 Mar 16; 168(6):281-3. [179] Cournoyer, op. cit., p. 42.[180] Whooping Cough, the DPT Vaccine and Reducing Vaccine Reactions. National Vaccine Information Center, Vienna, VA.[181] Miller DL, et al. Pertussis immunisation and serious acute neurological illness in children. Br Med J 1981 May 16; 282(6276):1595-9.[182] Gale JL, et al.  Risk of serious acute neurological illness after immunization with diphtheria-tetanus-pertussis vaccine. A population-based case-control study. JAMA 1994 Jan 5; 271(1):37-41.[183] Menkes JH, et al. Workshop on neurologic complications of pertussis and pertussis vaccination. Neuropediatrics 1990 Nov; 21(4):171-6.[184] Murphy JV, et al. Recurrent seizures after diphtheria, tetanus, and pertussis vaccine immunization. Onset less than 24 hours after vaccination. Am J Dis Child 1984 Oct; 138(10):908-11.[185] Stetler HC, et al. History of convulsions and use of pertussis vaccine. J Pediatr 1985 Aug; 107(2):175-9.[186] Hirtz DG, et al. Seizures following childhood immunizations. J Pediatr 1983 Jan; 102(1):14-8.[187] Odent MR, et al. Pertussis vaccination and asthma: is there a link? JAMA 1994 Aug 24-31; 272(8):592-3.[188] Farooqi IS, Hopkin JM. Early childhood infection and atopic disorder. Thorax 1998 Nov; 53(11):927-32).[189] McLaughlin SA, et al. Incidence of sudden infant death syndrome in Olmsted County, Minnesota: 1945 through 1992. Mayo Clin Proc 1995 Sep; 70(9):837-43.[190] Torch, WS. Diphtheria-pertussis-tetanus (DPT) immunization: a potential cause of the sudden infant death syndrome (SIDS). Neurology 1982; 32(4):A169 (abstract). [191] Torch WC. Diphtheria-pertussis-tetanus (DPT) immunization may be an unrecognized cause of sudden infant death (SIDS) and nearmiss syndrome (NMS): 12 case reports. Neurology 1986 b. (suppl 1); 36:149 (abstract). [192] Torch WC. Characteristics of diphtheria-pertussis-tetanus (DPT) postvaccinal deaths and DPT-caused sudden infant deaths syndrome (SIDS): a review. Neurology 1986 a (suppl 1); 36:148 (abstract). [193] Baraff LJ, et al. Possible temporal association between diphtheria-tetanus toxoid-pertussis vaccination and sudden infant death syndrome. Pediatr Infect Dis 1983 Jan-Feb; 2(1):7-11.[194] Walker AM, et al. Diphtheria-tetanus-pertussis immunization and sudden infant death syndrome. Am J Public Health 1987 Aug; 77(8):945-51.[195] Bakshi R, et al. Guillain-Barre syndrome after combined tetanus-diphtheria toxoid vaccination. J Neurol Sci 1997 Apr 15; 147(2):201-2. [196] Bolukbasi O, et al. Acute disseminated encephalomyelitis associated with tetanus vaccination. Eur Neurol1999; 41(4):231-2.[197] Read SJ, et al. Acute transverse myelitis after tetanus toxoid vaccination. Lancet 1992 May 2; 339(8801):1111-2. [198] Topaloglu H, et al. Optic neuritis and myelitis after booster tetanus toxoid vaccination. Lancet 1992 Jan 18; 339(8786):178-9. [199] Schlenska GK. Unusual neurological complications following tetanus toxoid administration. J Neurol 1977 Jul 20; 215(4):299-302. [200] Baust W, et al. Peripheral neuropathy after administration of tetanus toxoid. J Neurol 1979; 222(2):131-3. [201] Fardon DF. Unusual reactions to tetanus toxoid. JAMA 1967 Jan 9;199(2):125-6. [202] Rose I. Adverse reactions to tetanus toxoid. Lancet 1973 Feb 17; 1(7799):380. [203] Sutter RW. Adverse reactions to tetanus toxoid. JAMA 1994 May 25; 271(20):1629. [204] Centers for Disease Control and Prevention. Poliomyelitis prevention in the United States: updated recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR 2000 May 19; 49(RR-5):1-22.[205] Ibid.[206] Ibid.[207]www.cdc.gov/nip/vaccine/vacc-timeline.htm[208] Polio, An American Story:  The Crusade that Mobilized the Nation Against the 20th Century's Most Feared Disease p.27 http://www.cdc.gov/ncidod/dbmd/diseaseinfo/typhoidfever_g.htm[209] Polio, An American Story:  The Crusade that Mobilized the Nation Against the 20th Century's Most Feared Disease p.29 [210]http://www.wrongdiagnosis.com/contag/intro.htm[211] Polio, An American Story:  The Crusade that Mobilized the Nation Against the 20th Century's Most Feared Disease [212]http://www.wrongdiagnosis.com/contag/intro.htm[213]http://www.cdc.gov/ncidod/dbmd/diseaseinfo/cholera_g.htm#How%20does%20a%20person%20get%20cholera[214] Polio, An American Story:  The Crusade that Mobilized the Nation Against the 20th Century's Most Feared Disease [215] Kinnunen E, et al. Nationwide oral poliovirus vaccination campaign and the incidence of Guillain-Barre Syndrome. Am J Epidemiol 1998 Jan 1; 147(1):69-73 .[216] Uhari M, et al. Cluster of childhood Guillain-Barre cases after an oral poliovaccine campaign. Lancet 1989 Aug 19; 2(8660):440-1.[217] Friedrich F, et al. Temporal association between the isolation of Sabin-related poliovirus vaccine strains and the Guillain-Barre syndrome. Rev Inst Med Trop Sao Paulo 1996 Jan-Feb; 38(1):55-8.[218] Friedrich F. Rare adverse events associated with oral poliovirus vaccine in Brazil. Braz J Med Biol Res 1997 Jun; 30(6):695-703.[219] Ibid.[220] Fisher SG, et al. Cancer risk associated with simian virus 40 contaminated polio vaccine. Anticancer Res 1999 May-Jun; 19(3B):2173-80.[221] Martini F, et al. Simian-virus-40 footprints in human lymphoproliferative disorders of HIV- and HIV+ patients. Int J Cancer 1998 Dec 9; 78(6):669-74.[222] Ibid.[223] Martini F, et al. Simian virus 40 footprints in normal human tissues, brain and bone tumours of different histotypes. Dev Biol Stand 1998; 94:55-66.[224] Martini F, et al. SV40 early region and large T antigen in human brain tumors, peripheral blood cells, and sperm fluids from healthy individuals. Cancer Res 1996 Oct 15; 56(20):4820-5.[225] Huang H, et al. Identification in human brain tumors of DNA sequences specific for SV40 large T antigen. Brain Pathol 1999 Jan; 9(1):33-42.[226] Bergsagel DJ, et al. DNA sequences similar to those of simian virus 40 in ependymomas and choroid plexus tumors of childhood. N Engl J Med 1992 Apr 9; 326(15):988-93.[227] Testa JR, et al. A multi-institutional study confirms the presence and expression of simian virus 40 in human malignant mesotheliomas. Cancer Res 1998 Oct 15; 58(20):4505-9.[228] Galateau-Salle F, et al. SV40-like DNA sequences in pleural mesothelioma, bronchopulmonary carcinoma, and non-malignant pulmonary diseases. J Pathol 1998 Mar; 184(3):252-7.[229] Lednicky JA, et al. SV40 DNA in human osteosarcomas shows sequence variation among T-antigen genes. Int J Cancer 1997 Sep 4; 72(5):791-800.[230] Carbone M, et al. SV40-like sequences in human bone tumors. Oncogene 1996 Aug 1; 13(3):527-35.[231] Rizzo P, et al. Evidence for and implications of SV40-like sequences in human mesotheliomas and osteosarcomas. Dev Biol Stand 1998; 94:33-40.[232] Reactions of pediatricians to the recommendation for universal varicella vaccination. Newman RD, et al. Arch Pediatr Adolesc Med1998 Aug; 152(8):792-6. [233] Prevention of varicella. Update recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR 1999 May 28; 48(RR-6):1-5. [234]Pediatric News 33(3):12, 1999. [235] Connan L, et al. Intra-uterine fetal death following maternal varicella infection. Eur J Obstet Gynecol Reprod Biol 1996 Sep; 68(1-2):205-7. [236] Buchholz U, et al. Varicella outbreaks after vaccine licensure: should they make you chicken? Pediatrics 1999 Sep; 104(3 Pt 1):561-3. [237] Clements DA, et al. Over five-year follow-up of Oka/Merck varicella vaccine recipients in 465 infants and adolescents. Pediatr Infect Dis J 1995 Oct; 14(10):874-9. [238] Johnson CE, et al. A long-term prospective study of varicella vaccine in healthy children. Pediatrics 1997 Nov; 100(5):761-6. [239] Takayama N, et al. High incidence of breakthrough varicella observed in healthy Japanese children immunized with live attenuated varicella vaccine (Oka strain). Acta Paediatr Jpn 1997 Dec; 39(6):663-8. [240] Bernstein HH, et al. Clinical survey of natural varicella compared with breakthrough varicella after immunization with live attenuated Oka/Merck varicella vaccine. Pediatrics 1993 Dec; 92(6):833-7. [241] Clements, op. cit.[242] Johnson, op. cit.[243] Takayama, op. cit.[244] Halloran ME, et al. Theoretical epidemiologic and morbidity effects of routine varicella immunization of preschool children in the United States. Am J Epidemiol 1994 Jul 15; 140(2):81-104. [245] Gershon AA, et al. Varicella vaccine: the American experience. J Infect Dis 1992 Aug; 166 Suppl 1:S63-8.[246] Plotkin SA, et al. Zoster in normal children after varicella vaccine. J Infect Dis 1989 May; 159(5):1000-1. [247]N Engl J Med, September 11, 1989, p. 1333.[248] Fisher, Barbara Loe. The Consumer's Guide to Childhood Vaccines, National Vaccine Information Center, Vienna, VA, 1997.[249] Freed GL, Bordley WC, Clark SJ, Konrad TR. Family physician acceptance of universal hepatitis B immunization of infants. J Fam Pract 1993 Feb; 36(2):153-7.[250] Ibid.[251] Kinnersley P. Attitudes of general practitioners towards their vaccination against hepatitis B. BMJ 1990 Jan 27; 300(6719):238.[252] Burden AD, et al. Poor uptake of hepatitis B immunization amongst hospital-based health care staff. Postgrad Med J 1991 Mar; 67(785):256-8.[253] Freed GL, et al. Family physician acceptance of universal hepatitis B immunization of infants. J Fam Pract1993 Feb; 36(2):153-7.[254] Niu MT, Davis DM, Ellenberg S. Recombinant hepatitis B vaccination of neonates and infants: emerging safety data from the Vaccine Adverse Event Reporting System. Pediatr Infect Dis J 1996 Sep; 15(9):771-6.[255] Statement of the Association of American Physicians and Surgeons on Vaccines: Public Safety and Personal Choice before the Committee on Government Reform and Oversight U.S. House of Representatives. From www.aapsonline.org/aaps/[256] Incao, Philip, M.D. Letter to Representative Dale Van Vyven, Ohio House of Representatives. March 1, 1999. Provided to www.garynull.com by The Natural Immunity Information Network.[257] Dunbar B. Hearing before the Subcommittee on Criminal Justice, Drug Policy and Human Resources of the House Government Reform Committee. May 8, 1999, transcript by Federal News Service.[258] Hadler SC, et al. Long-term immunogenicity and efficacy of hepatitis B vaccine in homosexual men. N Engl J Med 1986 Jul 24; 315(4):209-14.[259] Pasko MT, et al. Persistence of anti-HBs among health care personnel immunized with hepatitis B vaccine. Am J Public Health 1990 May; 80(5):590-3.[260] Encephalitis after hepatitis B vaccination: recurrent disseminated encephalitis or MS? Neurology 1999 Jul 22; 53(2):396-401.[261] Herroelen L, et al. Central-nervous-system demyelination after immunisation with recombinant hepatitis B vaccine. Lancet 1991 Nov 9; 338(8776):1174-5.[262] Viral Hepatitis Prevention Board. Hepatitis B vaccine and central nervous system demyelinating diseases. Pediatr Infect Dis J 1999 Jan; 18(1):23-4. Review.[263] Nadler JP. Multiple sclerosis and hepatitis B vaccination. Clin Infect Dis 1993 Nov; 17(5):928-9.[264] Hall A, et al. Multiple sclerosis and hepatitis B vaccine? Vaccine 1999 Jun 4; 17(20-21):2473-5.[265] Birley HD, et al. Hepatitis B immunisation and reactive arthritis. BMJ 1994 Dec 3; 309(6967):1514.[266] Pope JE, et al. The development of rheumatoid arthritis after recombinant hepatitis B vaccination. J Rheumatol1998 Sep; 25(9):1687-93.[267] Bracci M, et al. Polyarthritis associated with hepatitis B vaccination. Br J Rheumatol 1997 Feb; 36(2):300-1.[268] Hachulla E, et al. Reactive arthritis after hepatitis B vaccination. J Rheumatol 1990 Sep; 17(9):1250-1.[269] Vautier G, et al. Acute sero-positive rheumatoid arthritis occurring after hepatitis vaccination. Br J Rheumatol1994 Oct; 33(10):991.[270] Grotto I, et al. Major adverse reactions to yeast-derived hepatitis B vaccines-a review. Vaccine 1998 Feb; 16(4):329-34.[271] Vaccinations: how safe and how effective, Nexus, August-September, 1993, p. 64. [272] Scheibner, Viera. Vaccination: 100 Years of Orthodox Research Shows that Vaccines Represent a Medical Assault on the Immune System, Maryborough, Victoria, Australia, Australian Print Group, 1993, p. 86-9.[273] Fiumara NJ, Etking PH. Mumps outbreak in Westwood, Massachusetts - 1981. Epidemiologic notes and reports. MMWR 1982; 33(29):421-30.[274] Ibid.[275] Cherry JD. The 'new' epidemiology of measles and Rubella. Hosp Practice 1980 Jul; 15(7):49-57.[276] Gustafson TL, et al., Measles outbreak in a fully immunized secondary-school population. NEJM 1987; 316(13):771-4.[277] Miller, Neil Z. Immunization Theory vs. Reality, The Atlantean Press, Santa Fe, NM, 1996, p. 82.[278] Scheibner, op. cit., p. 111.[279] Cherry, op. cit.[280] Fulginiti VA, et al. Altered reactivity to measles virus. Atypical measles in children previously immunized with inactivated measles virus vaccines. JAMA 1967; 202(12):1075-80. [281] Scott TF, Bonanno DE. Reactions to live-measles-virus vaccine in children previously inoculated with killed virus vaccine. N Engl J Med 1967; 277(5):248-51.[282] Rauh JL, et al. Rubella surveillance and vaccination at adolescence. American Journal Dis Child 1972; 124:27-8. [283] Howson CP, Fineberg HV. Adverse events following pertussis and rubella vaccines. summary of a report of the institute of medicine. JAMA 1992; 267(3):392-6. [284] Markowitz LE, Preblud SR, Orenstein WA, Rovira EZ, Adams NC, Hawkins CE, Hinman AR. Patterns of transmission in measles outbreaks in the United States, 1985-1986. N Engl J Med 1989; 32:75-81.[285]JAMA 1990 May 9; 263:2467-71.[286]MMWR 1989; 38:329-30. [287] National Health Federation Bulletin, November 1969.[288] Gary Null Interview with Jamie Murphy, December 18, 1997.[289] Murphy, Jamie. What Every Parent Should Know About Childhood Immunization, Boston, Earth Healing Products, 1993, p. 114.[290] Gary Null Interview with Jamie Murphy, April 7, 1995.[291] Scheibner, op. cit., p. 38.[292] Gary Null Interview with Meryl Dorey, December 17, 1997. [293] Sawada H, Yano S, Oka Y, Togashi T. Transmission of Urabe mumps vaccine between siblings. Lancet 1993 Aug 7; 342(8867):371.[294] Scheibner, op. cit., p. 92.[295]Sawada, op. cit.[296]Dorey M. The Australian Vaccination Network Newsletter, November 1997.[297]British Medical Journal, July 4, 1987.[298]http://www.cdc.gov/nip/vaccine/vacc-timeline.htm[299] Poland GA, et al. Failure to reach the goal of measles elimination. Apparent paradox of measles infections in immunized persons. Arch Intern Med 1994 Aug 22; 154(16):1815-20.[300] Miller E, et al. Antibodies to measles, mumps and rubella in UK children 4 years after vaccination with different MMR vaccines. Vaccine 1995 Jun; 13(9):799-802.[301] Whittle H, et al. Poor serologic responses five to seven years after immunization with high and standard titer measles vaccines. Pediatr Infect Dis J 1999 Jan; 18(1):53-7.[302] Maldonado YA, et al. Early loss of passive measles antibody in infants of mothers with vaccine-induced immunity. Pediatrics 1995 Sep; 96(3 Pt 1):447-50.[303] Wong RD, et al. Clinical and laboratory features of measles in hospitalized adults. Am J Med 1993 Oct; 95(4):377-83.[304] Auwaerter PG, Hussey GD, Goddard EA, Hughes J, et al. Changes within T cell receptor V beta subsets in infants following measles vaccination. Clin Immunol Immunopathol 1996 May; 79(2):163-70.[305] Ward BJ. Changes in cytokine production after measles virus vaccination: predominant production of IL-4 suggests induction of a Th2 response. Clin Immunol Immunopathol 1993 May; 67(2):171.[306] RESPONSE TO W.H.O. EVIDENCE FOR VACCINE SAFETY AND EFFECTIVENESS Trevor Gunn, BSc, RSHom [307] U.S. government statistic http://www.hhs.gov/news/press/pre1995pres/910000a.txt[308] E. Holt, et al from the Journal of Pediatrics, Vol. 85, No 2 pp188-194, February 1990   [309] (The lancet April 4, 1981 765). [310] , P. Aby, et Al, Pediat Infec DisJ 8: 197-200, 1989[311] Clemens et al, American Journal of Epidemiology, Vol 128, No. 6 1330-39[312]MMWR Morb Mortal Wkly Rep 1996 Sep 6; 45(RR-12):1-35.[313] Cheek JE, et al. Mumps outbreak in a highly vaccinated school population. Evidence for large-scale vaccination failure. Arch Pediatr Adolesc Med 1995 Jul;149(7):774-8.[314] Briss PA, et al. Sustained transmission of mumps in a highly vaccinated population: assessment of primary vaccine failure and waning vaccine-induced immunity. J Infect Dis 1994 Jan; 169(1):77-82.[315] Hersh BS, et al. Mumps outbreak in a highly vaccinated population. J Pediatr 1991 Aug; 119(2):187-93.[316] Zimmermann H, et al. Mumps epidemiology in Switzerland: results from the Sentinella surveillance system 1986-1993. Sentinella Work Group. German. Soz Praventivmed 1995; 40(2):80-92.[317] Matter L, et al. The incidence of rubella virus infections in Switzerland after the introduction of the MMR mass vaccination programme. Eur J Epidemiol 1995 Jun; 11(3):305-10.[318] Hillary IB, et al. Persistence of rubella antibodies 15 years after subcutaneous administration of Wistar 27/3 strain live attenuated rubella virus vaccine. JAMA 1981 Feb 20; 245(7):711-3.[319] Scheibner, op. cit., p. 111.[320]Cherry, op. cit., 49-57. [321] Howson CP, Fineberg HV. Adverse events following pertussis and rubella vaccines. summary of a report of the Institute of Medicine. JAMA 1992; 267(3):392-6. [322] Davis RL, et al.  MMR2 immunization at 4 to 5 years and 10 to 12 years of age: a comparison of adverse clinical events after immunization in the Vaccine Safety Datalink project. The Vaccine Safety Datalink Team. Pediatrics 1997 Nov; 100(5):767-71.[323] Miller D, et al. Measles vaccination and neurological events. Lancet 1997 Mar 8; 349(9053):730-1.[324] Sackey AH, et al. Hemiplegia after measles, mumps, and rubella vaccination. BMJ 1993 May 1; 306(6886):1169.[325] Kazarian EL, et al. Optic neuritis complicating measles, mumps, and rubella vaccination. Am J Ophthalmol 1978 Oct; 86(4):544-7.[326] Kline LB, et al. Optic neuritis and myelitis following rubella vaccination. Arch Neurol 1982 Jul; 39(7):443-4.[327] Akobeng AK et al. Inflammatory bowel disease, autism, and the measles, mumps, and rubella vaccine.  J Pediatr Gastroenterol Nutr 1999 Mar; 28(3):351-2.[328] Chiba Y, et al. Abnormalities of cellular immune response in arthritis induced by rubella vaccination. J Immunol 1976 Nov; 117(5 Pt 1):1684-7.[329] Tingle AJ, et al. Postpartum rubella immunization: association with development of prolonged arthritis, neurological sequelae, and chronic rubella viremia. J Infect Dis 1985 Sep; 152(3):606-12.[330] Roberts RJ, et al. Reasons for non-uptake of measles, mumps, and rubella catch up immunisation in a measles epidemic and side effects of the vaccine. BMJ 1995 Jun 24; 310(6995):1629-32.[331]http://165.112.6.70/exhibition/smallpox/sp_threat.html[332]http://165.112.6.70/exhibition/smallpox/sp_variolation.html[333] Miller, Neil Z. Immunization Theory vs. Reality, Santa Fe, NM, The Atlantean Press, 1996. [334] E. Jenner, Inquiry into the Causes and Effects of the Variolae Vaccine (London: Sampson Low, 1798) Case XVII [335] E. Jenner, Inquiry into the Causes and Effects of the Variolae Vaccine, p. 45. [336] summary of his practice in Bohn's Handbuch der Vaccination.   Leipzig, 1875, p. 82. [337] C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 6 p. 137-138 [338] E. Jenner, Inquiry into the Causes and Effects of the Variolae Vaccine, Case III [339] Salmade, La Pratique de I'Inoculation. Paris, An. vii. (1798) p. 51. [340] C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 2 p. 41. [341] J. Baron, Life of Jenner, i. p. 48. [342] C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 2 p. 23. [343] C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 2 p. 26.  [344] C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 2 p. 31. [345] C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 5 p. 123 [346]Contributions to Physical and Medical Knowledge, 1799 , p. 387. [347] C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 1 p. 8. [348] C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 1 p. 11. [349] C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 6 p. 150 [350] E. Jenner, Inquiry into the Causes and Effects of the Variolae Vaccine, general observations section of conclusion [351] J. Baron, Life of Jenner, ii. P304. [352] C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 6 p. 153- 154 [353] House of Commons, 17th June, 1840.  [354] C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 14 p. 339-340.  [355]Parliamentary Papers, vol. ci., 1852-53. [356] C. Ruata, A Summary of the Proofs That Vaccination Does Not Prevent Small-pox but Really Increases It (National Anti-Vaccination League S616: 1904) p. 8. [357] C. Ruata, A Summary of the Proofs That Vaccination Does Not Prevent Small-pox but Really Increases It (1904) p. 10. [358] C. Ruata, A Summary of the Proofs That Vaccination Does Not Prevent Small-pox but Really Increases It (1904) p. 10~11. [359] C. Creighton, JENNER AND VACCINATION - A Strange Chapter of Medical History, Chapter 14 p. 350 [360]Encyclopedia Britannica, Ninth Edition, 1888. subject: Vaccination, section: Influence of vaccination upon smallpox.Chart. [361] C. Ruata, A Summary of the Proofs That Vaccination Does Not Prevent Small-pox but Really Increases It (1904) p. 16~17. [362]http://www.informedchoice.info/cocktail.html[363]http://www.bt.cdc.gov/agent/smallpox/vaccination/live-virus.asp[364]http://165.112.6.70/exhibition/smallpox/sp_eradicate.html[365]http://www.cdc.gov/nip/vaccine/vacc-timeline.htm[366] Ibid.  [367] Intussusception Among Recipients of Rotavirus Vaccine-United States, 1998-1999. MMWR 1999 July 16; 48(27);577-81. [368] Rosenthal S, et al. The reporting sensitivities of two passive surveillance systems for vaccine adverse events. Am J Public Health1995; 85:1706-9. [369]http://www.rotavirusvaccine.org/documents/RotaShield_Fact_Sheet_CDC.pdf.[370] Michael Devitt, CDC Calls for Suspension of Childhood Rotavirus Vaccine "No One Should Now Be Giving Rotavirus Vaccine to Anyone." Dynamic Chiropractic October 4, 1999, Volume 17, Issue 21 http://www.chiroweb.com/archives/17/21/04.html[371] Parry, British Medical Journal, December 1, 1928, p.116.[372] Landrigan PJ, Witte JJ. Neurologic disorders following live measles-virus vaccination. JAMA 1973; 223(13):1459-62. [373] Pollock TM, et al. Symptoms after Primary Immunisation with DPT and with DT Vaccine. Lancet 1984 July; 21:146-9. [374] Hirtz DG, et al. Seizures Following Childhood Immunizations. Journal of Pediatrics 1983; 102(12):14-8. [375] Goldwater PN, et al. Sudden infant death syndrome: a possible clue to causation. Medical Journal Aust 1990; 153:59-60. [376] Goldwater PN, et al. Sudden infant death syndrome: a possible clue to causation. Medical Journal Aust 1990; 153:21-5.[377] Denborough MA, et al. Malignant Hyperpyrexia and Sudden Infant Death. Lancet 1982 Nov 13: 1068-72.[378] Chaitow, Leon. Vaccination and Immunization: Dangers, Delusions & Alternatives, Beekman Publishing, 1996.[379] Gary Null Report, November 15, 1994.[380] Coulter, Harris L and Fisher, Barbara Loe. A Shot in the Dark, Garden City Park, NY, Avery, 1991. [381] Merritt HH. Textbook of Neurology, Sixth Edition, Philadelphia, Lea and Febiger, 1979, p. 160.[382] Phillips, Alan. Vaccination: dispelling the myths. Nexus, October-November 1997.[383] National Technical Information Service, Springfield, VA. [384] Scheibner, Viera. Vaccination: 100 Years of Orthodox Research Shows that Vaccines Represent a Medical Assault on the Immune System, Maryborough, Victoria, Australia, Australian Print Group, 1993.[385] Torch WC. Diphtheria-pertussis-tetanus (DPT) immunization: a potential cause of the sudden infant death syndrome (SIDS). Neurology 1982; 32(4). [386] Scheibner, op. cit., p. 62.[387] Bafaff L, et al. Possible temporal association between diphtheria-tetanus toxoid-pertussis vaccination and sudden infant death syndrome. Pediatric Infectious Dis, 2, 1983, p. 7.[388] James, Walene. Immunization: The Reality Behind the Myth, Massachusetts, Bergin & Gervey, 1988.[389] Cournoyer, Cynthis. What About Immunizations?, 6th Edition, Nelson's Books, 1995, p. 34.[390]Immunization, Special Edition, Santa Fe, NM, Mothering Publications, 1984.[391] Moskowitz R. The Case Against Immunizations, Washington, DC, National Center for Homeopathy.[392] Cournoyer, op. cit., p. 35.[393] Scheibner, op. cit., p. 88-9.[394] Black FL, et al. Inadequate Immunity to Measles Immunity in Era of Vaccine-Protected Mothers. Bull WHO1984; 62(92):315-9.[395] Lennon JL, Black FL. Maternally derived measles immunity in era of vaccine-protected mothers. Journal of Pediatrics 1986; 108(1):671-6.[396] Scheibner, op. cit., p. 199.[397] Aaby P, et al. Long-term survival after Edmonston-Zagreb measles vaccination in Guinea-Bissau: increased female mortality rate. J Pediatr 1993 Jun; 122(6):904-8.[398] Garenne M, et al. Child mortality after high-titre measles vaccines: prospective study in Senegal. Lancet 1991 Oct 12; 338(8772):903-7.[399] Cournoyer, op. cit., p. 160.[400] "Interview with Barbara Loe Fisher." National Vaccine Information Center Newsletter Website.[401] Cournoyer, op. cit., p. 156.[402] The National Childhood Vaccine Injury Act of 1986 Public Law 99-690, The Compensation System and How it Works. The National Vaccination Information Center, Vienna, VA, 1990.[403] Vaccine injury compensation program statistics. NVIC News, August 1994, p. 10.[404] Phillips, op. cit.[405] National Vaccine Injury Compensation Program, Health Resources and Services Administration, Rockville, MD.[406] Neustaedter R. Do vaccines disable the immune system? Internet Document.[407] Fisher, Barbara Loe. The Consumer's Guide to Childhood Vaccines, Vienna, VA, National Vaccine Information Center, 1997.[408] Ibid, p. 48.[409] Ibid, p. 64.[410] National Vaccine Injury Compensation Program: monthly statistics report, September 30, 2002. U.S. Department of Health and Human Services, Health Resources and Services Administration. From www.hrsa.gov/osp/vicp/monthly.htm.[411] Gary Null Interview with Barbara Loe Fisher, April 11, 1995.[412] Ibid.[413] Gary Null Interview with Dr. Dean Black, April 7, 1995. [414] Gary Null Interview with Curtis Cost, December 17, 1997.[415] Gary Null Interview with Barbara Loe Fisher, April 11, 1995.[416] Gary Null Interview with Alan Phillips, December 17, 1997.[417] Gary Null Interview with Dr. Dean Black, April 7, 1995. 

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