Sunday, July 10, 2011

TRUTH BEHIND THE VACCINE COVER-UP

THE TRUTH BEHIND THE VACCINE COVER-UP
By Dr. Russell Blaylock, M.D. www.russellblaylockmd.com
(c) 2004 Reprinted from sydney.indymedia.org/display.php3?article_id=45874&group=webcast and Dr. Mercola's site - www.mercola.com/2004/sep/22/blaylock_vaccine_coverup.htm

I was asked to write a paper on some of the newer mechanisms of vaccine damage to the nervous system, but in the interim I came across an incredible document that should blow the lid off the cover-up being engineered by the pharmaceutical companies in conjunction with powerful governmental agencies.

It all started when a friend of mind sent me a copy of a letter from Congressman David Weldon, M.D. to the director of the CDC, Dr Julie L. Gerberding, in which he alludes to a study by a Doctor Thomas Verstraeten, then representing the CDC, on the connection between infant exposure to thimerosal-containing vaccines and neurodevelopmental injury. In this shocking letter Congressman Weldon referrers to Dr. Verstraeten's study which looked at the data from the Vaccine Safety Datalink and found a significant correlation between thimerosal exposure via vaccines and several neurodevelopmental disorders including tics, speech and language delays, and possibly to ADD.

Congressman Weldon questions the CDC director as to why, following this meeting, Dr. Verstraeten published his results, almost four years later, in the journal Pediatrics to show just the opposite, that is, that there was no correlation to any neurodevelopmental problems related to thimerosal exposure in infants. In this letter, Congressman Weldon refers to a report of the minutes of this meeting held in Georgia, which exposes some incredible statements by the "experts" making up this study group. The group's purpose was to evaluate and discuss Dr. Verstraeten's results and data and make recommendation that would eventually lead to possible alterations in the existing vaccine policy.

I contacted Congressman Weldon's legislative assistant and he kindly sent me a complete copy of this report. Now, as usual in these cases, the government did not give up this report willingly, it required a Freedom of Information Act lawsuit to pry it loose. Having read the report twice and carefully analyzed it; I can see why they did not want any outsiders to see it. It is a bombshell, as you shall see. In this analysis, I will not only describe and discuss this report, but also will frequently quote their words directly and supply the exact page number so others can see for themselves.

The official title of the meeting was the "Scientific Review of Vaccine Safety Datalink Information." This conference, held on June 7-8, 2000 at Simpsonwood Retreat Center, Norcross, Georgia, assembled 51 scientists and physicians of which five represented vaccine manufacturers. These included Smith Kline Beecham, Merck, Wyeth, North American Vaccine and Aventis Pasteur.

During this conference, these scientists focused on the study of the Datalink material, whose main author was Dr. Thomas Verstraesten who identified himself as working at the National Immunization Program of the CDC. It was discovered by Congressman Weldon that Dr. Verstraeten left the CDC shortly after this conference to work for GlaxoSmithKline in Belgium which manufacturers vaccines, a recurring pattern that has been given the name a "revolving door" It is also interesting to note that GlaxoSmithKline was involved in several lawsuits over complications secondary to their vaccines.

To start off the meeting Dr. Roger Bernier, Associate Director for Science in the National Immunization Program (CDC), related some pertinent history. He stated that Congressional action in 1977 required that the FDA review mercury being used in drugs and biologics (vaccines). In meeting this order, the FDA called for information from the manufacturers of vaccines and drugs. He notes that a group of European regulators and manufacturers met on April 1999 and noted the situation but made no recommendations of changes. In other words it was all for show.

At this point Dr. Bernier made an incredible statement (page 12). He said, "In the United States there was a growing recognition that cumulative exposure may exceed some of the guidelines." By guidelines, he is referring to guidelines for mercury exposure safety levels set by several regulatory agencies. The three guidelines were set by the ATSDR, the FDA and the EPA. The most consistently violated safety guideline was that set by the EPA. He further explains that he is referring to children being exposed to thimerosal in vaccines.

Based on this realization that they were violating safety guidelines he says, this then "resulted in a joint statement of the Public Health Service (PHS) and the American Academy of Pediatrics (AAP) in July of last year (1999), which stated that as a long term goal, it was desirable to remove mercury from vaccines because it was a potentially preventable source of exposure."(Page 12)

As an aside, one has to wonder, where was the Public Health Service and American Academy of Pediatrics during all the years of mercury use in vaccines and why didn't they know that, number one, they were exceeding regulatory safety levels and second, why weren't they aware of the extensive literature showing deleterious effects on the developing nervous system of babies? As we shall see even these "experts" seem to be cloudy on the mercury literature.

Dr. Bernier notes that in August 1999 a public workshop was held at Bethesda in the Lister Auditorium by the National Vaccine Advisory Group and the Interagency Working Group on Vaccines to consider thimerosal risk in vaccine use. And based on what was discussed in that conference, thimerosal was removed from the hepatitis B vaccine (HepB). It is interesting to note that the media took very little interest in what was learned at that meeting and it may have been a secret meeting as well. As we shall see, there is a reason why they struggle to keep the contents of all these meetings secret from the public.

He then notes on page 13 that on October 1999 the Advisory Committee on Immunization Practices (ACIP) "looked this situation over again and did not express a preference for any of the vaccines that were thimerosal free." In this discussion he further notes that the ACIP concluded that the thimerosal-containing vaccines could be used but the "long-term goal" is to try to remove thimerosal as soon as possible.

Now, we need to stop and thinks about what has transpired here. We have an important group here; the ACIP that essential plays a role in vaccine policy that affects tens of millions of children every year. And, we have evidence from the Thimerosal meeting in 1999 that the potential for serious injury to the infant's brain is so serious that a recommendation for removal becomes policy. In addition, they are all fully aware that tiny babies are receiving mercury doses that exceed even EPA safety limits, yet all they can say is that we must "try to remove thimerosal as soon as possible". Do they not worry about the tens of millions of babies that will continue receiving thimerosal-containing vaccines until they can get around to stopping the use of thimerosal?

It should also be noted that it is a misnomer to say "removal of thimerosal" since they are not removing anything. They just plan to stop adding it to future vaccines once they use up existing stocks, which entails millions of doses. And, incredibly, the government allows them to do it. Even more incredibly, the American Academy of Pediatrics and the American Academy of Family Practice similarly endorse this insane policy. In fact, they specifically state that children should continue to receive the thimerosal-containing vaccines until new thimerosal-free vaccine can be manufactured at the will of the manufacturers. Are they afraid that there will be a sudden diphtheria epidemic in America or tetanus epidemic?

The most obvious solution was to use only single-dose vials, which requires no preservative. So, why don't they use them? Oh, they exclaim, it would add to the cost of the vaccine. Of course, we are only talking about a few dollars per vaccine at most, certainly worth the health of your child's brain and future. They could use some of the hundreds of millions of dollars they waste on vaccine promotion every year to cover these cost for the poor. Then, that would cut into some fat-cat's budget and we can't have that.

It was disclosed that thimerosal was in all influenza vaccines, DPT (and most DtaP) vaccines and all HepB vaccines.

As they begin to concentrate on the problem at hand we first begin to learn that the greatest problem with the meeting is that, they know virtually nothing about what they are doing. On page 15, for example, they admit that there is very little pharmacokinetic data on ethylmercury, the form of mercury in thimerosal. In fact they say there is no data on excretion, the data on toxicity is sparse, yet it is recognized to cause hypersensitivity, it can cause neurological problems and even death, and it is known to easily pass the blood-brain barrier and the placental barrier.

Therefore, what they are admitting is that we have a form of mercury that has been used in vaccines since the 1930s and no one has bothered to study the effects on biological systems, especially the brain of infants. Their defense throughout this conference is "we just don't know the effects of ethylmercury." As a solution, they resort to studies on methylmercury, because there are thousands of studies on this form of mercury. The major source of this form is seafood consumption.

It takes them awhile to get the two forms of mercury straight, since for several pages of the report they say methylmercury is in thimerosal rather than ethylmercury. They can be forgiven for this. On page 16, Dr. Johnson, an immunologist and pediatrician at the University of Colorado School of Medicine and the National Jewish Center for Immunology and Respiratory Medicine, notes that he would like to see the incorporation of wide margins of safety, that is 3 to 10-fold margins of safety to "account for data uncertainties." What he means is that there are so many things we do not know about this toxin that we had better use very wide margins of safety. For most substances the FDA uses a 100-fold margin of safety.

The reason for this, which they do not mention, is that in a society of hundreds of millions of people there are groups of people who are much more sensitive to the toxin than others. For instance, the elderly, the chronically ill, the nutritionally deficient, small babies, premature babies, those on certain medications and inborn defects in detoxification, just to name a few. In fact, in this study they excluded premature babies and low birth weight babies from the main study, some of which had the highest mercury levels, because they would be hard to study and because they had the most developmental problems related to the mercury.

On page 16 as well Dr. Johnson make an incredible statement, one that defines the problem we have in this country with the promoters of these vaccines. He states, "As an aside, we found a cultural difference between vaccinologist and environmental health people in that many of us in the vaccine arena have never thought about uncertainty factors before. We tend to be relatively concrete in our thinking." Then he says, "One of the big cultural events in that meeting ---was when Dr. Clarkson repetitively pointed out to us that we just didn't get it about uncertainty, and he was actually quite right." This is an incredible admission. First, what is a vaccinologist? Do you go to school to learn to be one? How many years of residency training are required to be a vaccinologist? Are there board exams? It's a stupid term used to describe people who are obsessed with vaccines, not that they actually study the effects of the vaccines, as we shall see throughout this meeting. Most important is the admission by Dr. Johnson that he and his fellow "vaccinologist" are so blinded by their obsession with forcing vaccines on society that they never even considered that there might be factors involved that could greatly affect human health, the so-called "uncertainties." Further, that he and his fellow "vaccinologist" like to think in concrete terms-that is, they are very narrow in their thinking and wear blinders that prevent them from seeing the numerous problems occurring with large numbers of vaccination in infants and children. Their goal in life is to vaccinate as many people as possible with an ever-growing number of vaccines.

On page 17 his "concrete thinking" once again takes over. He refers to the Bethesda meeting on Thimerosal safety issues and says, "there was no evidence of a problem, only a theoretical concern that young infants' developing brains were being exposed to an organomercurial." Of course, as I shall point out later, it is a lot more than a "theoretical concern". He then continues by saying, "We agree that while there was no evidence of a problem the increasing number of vaccine injections given to infants was increasing the theoretical mercury exposure risk."

It's hard to conceive of a true scientist not seeing the incredible irony of these statements. The medical literature is abound with studies on the deleterious effects of mercury on numerous enzymes, mitochondrial energy production, synaptic function, dendritic retraction, neurotubule dissolution and excitotoxicity, yet, he sees only a "theoretical risk" associated with an ever increasing addition of thimerosal-containing vaccines. It is also important to note that these geniuses never even saw a problem in the first place, it was pressure from outside scientists, parents of affected children and groups representing them that pointed out the problem. They were, in essence, reacting to pressure from outside the "vaccinologist club" and not discovering internally that a problem "might" exist.

In fact, if these outside groups had not become involved these "vaccinologists" would have continued to add more and more mercury-containing vaccines to the list of required vaccines. Only when the problem became so obvious, that is of epidemic proportion (close to that now) and the legal profession became involved would they have even noticed there was a problem. This is a recurring theme in the government's regulatory agencies, as witnessed with fluoride, aspartame, MSG, dioxin and pesticides issues.

It is also interesting that Dr. Johnson did admit that the greatest risk was among low birth weight infants and premature infants. Now why would that be if there existed such a large margin of safety with mercury used in vaccines? Could just a few pounds of body weight make such a dramatic difference? In fact, it does but it also means that normal birth weight children, especially those near the low range of normal birth weight, are also in greater danger. It also would mean that children receiving doses of mercury higher than the 72 ug in this study would be at high risk as well because their dose, based on body weight, would be comparable to that of the low birth weight child receiving the lower dose. This is never even considered by these "vaccinologist experts" who decide policy for your children.

Now this next statement should shock everyone, but especially the poor who in any way think that these "vaccinologists" experts have their best interest in mind. Dr. Johnson says on page 17, "We agree that it would be desirable to remove mercury from U.S. licensed vaccines, but we did not agree that this was a universal recommendation that we would make because of the issue concerning preservatives for delivering vaccines to other countries, particularly developing countries, in the absence of hard data that implied that there was in fact a problem."

So, here you have it. The data is convincing enough that the American Academy of Pediatrics and the American Academy of Family Practice, as well as the regulatory agencies and the CDC along with these organization all recommend its removal as quickly as possible because of concerns of adverse effects of mercury on brain development, but not for the children in the developing countries. I thought the whole idea of child health programs in the United States directed toward the developing world was to give poor children a better chance in an increasingly competitive world. This policy being advocated would increase the neurodevelopmental problems seen in poor children (also in this country) of developing countries, impairing their ability to learn and develop competitive minds. Remember, there was a representative of the World Health Organization (WHO), Dr. John Clements, serving on this panel of "experts". He never challenged this statement made by Dr. Johnson.

It also needs to be appreciated that children in developing countries are at a much greater risk of complications from vaccinations and from mercury toxicity than children in developed countries. This is because of poor nutrition, concomitant parasitic and bacterial infections and a high incidence of low birth weight in these children. We are now witnessing a disaster in African countries caused by the use of older live virus polio vaccines that has now produced an epidemic of vaccine related polio, that is, polio caused by the vaccine itself. In, fact, in some African countries, polio was not seen until the vaccine was introduced.

The WHO and the "vaccinologist experts" from this country now justify a continued polio vaccination program with this dangerous vaccine on the basis that now that they have created the epidemic of polio, they cannot stop the program. In a recent article it was pointed out that this is the most deranged reasoning, since more vaccines will mean more vaccine-related cases of polio. But then, "vaccinologist" have difficulty with these "uncertainties". (Jacob JT. A developing country perspective on vaccine-associated paralytic poliomyelitis. Bulletin WHO 2004; 82: 53-58. See commentary by D.M. Salisbury at the end of the article.)

Then he again emphasizes the philosophy that the health of children is secondary to "the program" when he says, "We saw some compelling data that delaying the birth dose of HepB vaccine would lead to significant disease burden as a consequence of missed opportunity to immunize." This implies that our children would be endangered from the risk of hepatitis B should the vaccine program stop vaccinating newborns with the HepB vaccine.

In fact, this statement is not based on any risk to U.S. children at all and he makes that plain when he states, "that the potential impact on countries that have 10% to 15% newborn hepatitis B exposure risk was very distressing to consider." (page 18) In other words the risk is not to normal U.S. children but to children in developing countries. In fact, hepatitis B is not a risk until the teenage years and after in this country. The only at-risk group among children is with children born to drug using parents; mothers infected with hepatitis B or HIV infected parents. The reason for vaccinating the newborns is to capture them before they can escape the "vaccinologist's" vaccine program.

This is a tactic often used to scare mothers into having their children vaccinated. For example, they say that if children are not vaccinated against measles millions of children could die during a measles epidemic. They know this is nonsense. What they are using is examples taken from developing countries with poor nutrition and poor immune function in which such epidemic death can occur. In the United States we would not see this because of better nutrition, better health facilities and better sanitation. In fact, most deaths seen when measles outbreaks occur in the United States occur either in children in which vaccination was contraindicated, the vaccine did not work or in children with chronic, immune-suppressing diseases.

In fact, in most studies these children catching the measles or other childhood diseases have been either fully immunized or partially immunized. The big secret among "vaccinologists" is that anywhere from 20 to 50% of children are not resistant to the diseases for which they have been immunized.

Also on page 18, Dr. Johnson tells the committee that it was Dr. Walt Orenstein who "asked the most provocative question which introduced a great deal of discussion. That was, should we try to seek neurodevelopmental outcomes fro children exposed to varying doses of mercury by utilizing the Vaccine Safety Datalink data from one or more sites." (page 18)

I take from this no one had ever even thought of looking at the data that had just been sitting there all these years un-reviewed. Children could have been dropping like flies or suffering from terrible neurodevelopmental defects caused by the vaccine program and no one in the government would have known. In fact, that is exactly what the data suggested was happening, at least as regards neurodevelopmental delays.

We should also appreciate that the government sponsored two conferences on the possible role of metals, aluminum and mercury, being use in vaccines without any change in vaccine policy occurring after the meetings. These meetings were held a year before this meeting and before any examination of the data which was being held tightly by the CDC, (which was denied to other independent, highly qualified researchers). I will talk more about what was discussed in the aluminum conference later. It is very important and is only briefly referred to in this conference for a very good reason. If the public knew what was discussed at the aluminum meeting no one would ever get a vaccination using the presently manufactured types of vaccines again.

Despite what was discussed in the aluminum meeting and the scientific literature on the neurotoxicity of aluminum, Dr. Johnson makes the following remark; "Aluminum salts have a very wide margin of safety. Aluminum and mercury are often simultaneously administered to infants, both at the same site and at different sites." Also on page 20, he states, "However, we also learned that there is absolutely no data, including animal data, about the potential for synergy, additively or antagonism, all of which can occur in binary metal mixtures..."

It is important her to appreciate a frequently used deception by those who are trying to defend an indefensible practice. They use the very same language just quoted, that is, that there is no data to show, etc, etc. They intend it to convey the idea that the issue has been looked at and studied thoroughly and no toxicity was found. In truth, it means that no one has looked at this possibility and there have been no studies that would give us an answer one way or the other.

In fact, we know that aluminum is a significant neurotoxin and that it shares many common mechanisms with mercury as a neurotoxin. For example, they are both toxic to neuronal neurotubules, interfere with antioxidant enzymes, poison DNA repair enzymes, interfere with mitochondrial energy production, block the glutamate reuptake proteins (GLT-1 and GLAST), bind to DNA, and interfere with neuronal membrane function. Toxins that share toxic mechanisms are almost always additive and frequently synergistic in their toxicity. So, Dr. Johnson's statement is sheer nonsense.

A significant number of studies have shown that both of these metals play a significant role in all of the neurodegenerative disorders. It is also important to remember, both of these metals accumulate in the brain and spinal cord. This makes them accumulative toxins and therefore much more dangerous than rapidly excreted toxins.

To jump ahead, on page 23 Dr, Tom Sinks, Associate Director for Science at the National Center for Environmental Health at the CDC and the Acting Division Director for Division of Birth Defects, Developmental Disabilities and Health, ask, "I wonder is there a particular health outcome that is related to aluminum salts that may have anything that we are looking at today?" Dr. Martin Meyers, Acting Director of the National Vaccine Program Office, answers, "No, I don't believe there are any particular health concerns that was raised." This is after an aluminum conference held the previous year that did indeed find significant health concerns and an extensive scientific literature showing aluminum to be of great concern.

On page 24 Dr. William Weil, a pediatrician representing the Committee on Environmental Health of the American Academy of Pediatrics, brings some sense to the discussion by reminding them that, "there are just a host of neurodevelopmental data that would suggest that we've got a serious problem. The earlier we go, the more serious the problem." Here he means that the further back you go during the child's brain development, the more likely the damage to the infant. I must give him credit; at least he briefly recognized that a significant amount of brain development does take place later. He also reminds his collogues that aluminum produced severe dementia and death in dialysis cases. He concludes by saying, "To think there isn't some possible problem here is unreal." (page 25)

Not to let it end there, Dr. Meyers adds, "We held the aluminum meeting in conjunction with the metal ions in biology and medicine meeting, we were quick to point out that in the absence of data we didn't know about additive or inhibitory activities." Once again we see the "no data" ploy. There is abundant data on the deleterious effects of aluminum on the brain, a significant portion of which came out in that very meeting.

Dr. Johnson also quotes Dr. Thomas Clarkson, who identifies himself as associated with the mercury program at the University of Rochester, as saying that delaying the HepB vaccine for 6 months or so would not affect the mercury burden. (page 20). He makes the correct conclusion when he says, "I would have thought that the difference was in the timing. That is you are protecting the first six months of the developing central nervous system."

Hallelujah, for a brief moment I thought that they had stumbled on one of the most basic concepts in neurotoxicology. Then Dr. Meyers dashed my hopes by saying that single, separated doses would not affect blood levels at all. At this juncture, we need a little enlightenment. It is important to appreciate that mercury is a fat soluble metal. That is, it is stored in the body's fat. The brain contains 60% fat and therefore is a common site for mercury storage. Now, they establish in this discussion that about half of methylmercury is excreted over several months when ingested. A recent study found that ethylmercury has a half-life of 7 days.

Even so, a significant proportion of the mercury will enter the brain (it has been shown to easily pass through the blood-brain barrier) where it is stored in the phospholipids (fats). With each new dose, and remember these children are receiving as many as 22 doses of these vaccines, another increment is added to the brain storage depot. This is why we call mercury an accumulative poison. They never once, not once, mention this vital fact throughout the entire conference. Not once. Moreover, they do so for a good reason, it gives the unwary, those not trained in neuroscience, assurance that all that matters here is blood levels.

In fact, on page 163, Dr. Robert Brent, A developmental biologist and pediatrician at the Thomas Jefferson University and Dupont Hospital for Children, says that we don't have data showing accumulation and "that with the multiple exposures you get an increasing level, and we don't know whether that is true or not." He redeems himself somewhat by pointing out that some of the damage is irreversible and with each dose more irreversible damage occurs and in that way it is accumulative.

On page 21 Dr. Thomas Clarkson makes the incredible statement implying that he knows of no studies that shows exposure to mercury after birth or at six months would have deleterious effects. Dr. Isabelle Rapin, a neurologist for children at Albert Einstein College of Medicine, follows up by saying that "I am not an expert on mercury in infancy" but she knows it can affect the nerves (peripheral nervous system). So, here is one of our experts admitting that she knows little about the effects of mercury on the infant. My question is-Why is she here? Dr. Rapin is a neurologist for children at Albert Einstein College of Medicine who stated that she has a keen interest in developmental disorders, in particular those involving language and autism, yet she knows little about the effects on mercury on the infant brain.

This conference is concerned with the effects of mercury in the form of thimerosal on infant brain development, yet throughout this conference our experts, especially the "vaccinologists" seem to know little about mercury except limited literature that shows no toxic effects except at very high levels. None of the well known experts were invited, such as Dr. Ascher from Bowman Grey School of Medicine or Dr. Haley Boyd, who has done extensive work on the toxic effects of low concentrations on the CNS. They were not invited because they would be harmful to the true objective of this meeting, and that was to exonerate mercury in vaccines.

Several times throughout this conference, Dr. Brent reminds everyone that the most sensitive period for the developing brain is during the early stages of pregnancy. In fact, he pinpoints the 8th to 18th week as the period of neuromaturation. In fact, the most rapid period of brain maturation, synaptic development and brain pathway development is during the last three months of pregnancy continuing until two years after birth. This is often referred to as the "brain growth spurt." This is also not mentioned once in this conference, again because if mothers knew that their child's brain was busy developing for up to two years after birth they would be less likely to accept this safety of mercury nonsense these "vaccinologists" proclaim.

The brain develops over 100 trillion synaptic connections and tens of trillions of dendritic connections during this highly sensitive period. Both dendrites and synapses are very sensitive, even to very low doses of mercury and other toxins. It has also been shown that subtoxic doses of mercury can block the glutamate transport proteins that play such a vital role in protecting the brain against excitotoxicity. Compelling studies indicate that damage to this protective system plays a major role in most of the neurodegenerative diseases and abnormal brain development as well.

Recent studies have shown that glutamate accumulates in the brains of autistic children, yet these experts seem to be unconcerned about a substance (mercury) that is very powerful in triggering brain excitotoxicity.

It is also interesting to see how many times Dr. Brent emphasizes that we do not know the threshold for mercury toxicity for the developing brain. Again, that is not true-we do know and the Journal of Neurotoxicology states that anything above 10ug is neurotoxic. The WHO in fact states that there is no safe level of mercury.

On page 164 Dr. Robert Davis, Associate Professor of Pediatrics and Epidemiology at the University of Washington, makes a very important observation. He points out that in a population like the United States you have individuals with varying levels of mercury from other causes (diet, living near coal burning facilities, etc.) and by vaccinating everyone you raise those with the highest levels even higher and bring those with median levels into a category of higher levels. The "vaccinologists" with their problem of "concrete thinking" cannot seem to appreciate the fact that not everyone is the same. That is, they fail to see these "uncertainties".

To further emphasize this point lets take a farming family who lives within three miles of a coal-burning electrical plant. Since they also live near the ocean they eat seafood daily. The fertilizers, pesticides and herbicides used on the crops contain appreciable levels of mercury. The coal-burning electrical plant emits high levels of mercury in the air they breathe daily and the seafood they consume has levels of mercury higher than EPA safety standards. This means that any babies born to these people will have very high mercury levels.

Once born, they are given numerous vaccines containing even more mercury, thereby adding significantly to their already high mercury burden. Are these "vaccinologists" trying to convince us that these children don't matter and that they are to be sacrificed at the alter of the "vaccine policy"?

Recent studies by neurotoxicologists have observed that as our ability to detect subtle toxic effects improves, especially on behavior and other neurological functions, we lower the level of acceptable exposure. In fact, Dr, Sinks brings up that exact point, using lead as an example. He notes that as our neurobehavioral testing improved, we lowered the acceptable dose considerably and continues to do so. Dr. Johnson had the audacity to add, " The smarter we get, the lower the threshold." Yet, neither he, nor the other participants seem to be getting any smarter concerning this issue.

Dr. Robert Chen, Chief of Vaccine Safety and Development at the National Immunization Program at the CDC, then reveals why they refuse to act on this issue, he says, "the issue is that it is impossible, unethical to leave kids unimmunized, so you will never, ever resolve that issue. So then we have to refer back from that." (page 169) In essence, immunization of the kids takes precedence over safety concerns with the vaccines themselves. If the problem of vaccine toxicity cannot be solved, he seems to be saying, then we must accept that some kids will be harmed by the vaccines.

Dr. Brent makes the statement that he knows of no known genetic susceptibility data on mercury and therefore assumes there is a fixed threshold of toxicity. That is, that everyone is susceptible to the same dose of mercury and there are no genetically hypersensitive groups of people. In fact, a recent study found just such a genetic susceptibility in mice. In this study they found that mice susceptible to autoimmunity developed neurotoxic effects to their hippocampus, including excitotoxicity, not seen in other strains of mice. They even hypothesize that the same may be true in humans, since familial autoimmunity increases the likelihood of autism in offspring. (Hornig M, Chian D, Lipkin WI. Neurotoxic effects of postnatal thimerosal are mouse strain dependent. Mol Psychiatry 2004; (in press).

For the next quotation you need a little discussion to be able to appreciate the meaning. They are discussing the fact that in Dr. Verstraeten study frightening correlations were found between the higher doses of thimerosal and problems with neurodevelopment, including ADD and autism. The problem with the study was that there were so few children who had received no thimerosal-containing vaccines that a true control group could not be used. Instead they had to use children getting 12.5ug of mercury as the control and some even wanted to use the control dose as 37.5ug. So the controls had mercury levels that could indeed cause neurodevelopmental problems. Even with this basic flaw, a strong positive correlation was found between the dose of mercury given and these neurodevelopmental problems.

It was proposed that they compare a group of children receiving non-thimerosal vaccines to those who had. In fact, we later lean that they had a large group of children who could have been used as a thimerosal-free control. It seems that for two years before this conference the Bethesda Naval Hospital had been using only thimerosal-free vaccines to immunize the children. They knew this and I would assume someone would have told Dr. Verstraeten of this important fact before he did his study.

So, now to the quote. Dr. Braun responds to the idea of starting a new study using such thimerosal-free controls by saying, "Sure we will have the answer in five years. The question is what can we do now with the data we have?" (page 170). Well, we have the answer to that, they simply covered this study up, declare that thimerosal is of no concern and continue the unaltered policy. That is, they can suggest the pharmaceutical manufacturers of vaccines remove the thimerosal but not making it mandatory or examining the vaccine to make sure they have removed it.

Lets us take a small peak at just how much we can trust the pharmaceutical manufacturers to do the right thing. Several reports of major violations of vaccine manufacturing policy have been cited by the regulatory agencies have surfaced. This includes obtaining plasma donations without taking adequate histories on donors as to disease exposures and previous health problems, poor record keeping on these donors, improper procedures and improper handing of specimens.

That these are not minor violations is emphasized by the discovery that a woman with variant Mad Cow Disease was allowed to given plasma to be used in vaccines in England. In fact, it was learned only after the contaminated plasma was pooled and used to make millions of doses of vaccines that her disease was discovered. British health officials told the millions of vaccinated not to worry, since we have no idea if it will really spread the disease.

Contamination of vaccines is a major concern in this country as well, as these regulatory violations make plain. It is also important to note that no fines were given, just warnings.

Conclusions By The Study Group

At the end of the conference, a poll was taken asking two questions. One was do you think that there is sufficient data to make a causal connection between the use of thimerosal-containing vaccines and neurodevelopmental delays? Second, do you think further study is called for based on this study?

First, let us see some of the comments on the question of doing further studies. Dr. Paul Stehr-Green, Associate Professor of Epidemiology at the University of Washington School of Public Health and Community Medicine, who voted yes, gave as his reason, "The implications are so profound these should be examined further." (page 180) Meanwhile, Dr. Brent interjects his concern that the lawyers will get hold of this information and begin filing lawsuits. He says, "They want business and this could potentially be a lot of business." (Page 191)

Dr. Loren Koller, Pathologist and Immunotoxicologist at the College of Veterinary Medicine, Oregon State University, is to be congratulated in that he recognized that more is involved in the vaccine effects than just ethylmercury. (page 192). He mentions aluminum and even the viral agents beings used as other possibilities. This is especially important in the face of Dr. RK Gherardi's identification of macrophagic myofascitis, a condition causing profound weakness and multiple neurological syndromes, one of which closely resembled multiple sclerosis. Both human studies and animal studies have shown a strong causal relationship to the aluminum hydroxide or aluminum phosphate used as a vaccine adjuvants. More than 200 cases have been identified in European countries and the United States and has been described as an "emerging condition".

Here are some of the neurological problems seen with the use of aluminum hydroxide and aluminum phosphate in vaccines. In two children aged 3 and 5, doctors at the All Children's Hospital in St. Petersburg, Florida described chronic intestinal pseudo-obstruction, urinary retention and other findings indicative of a generalized loss of autonomic nervous system function (diffuse dysautonomia). The 3-year old had developmental delay and hypotonia (loss of muscle tone). A biopsy of the children's vaccine injection site disclosed elevated aluminum levels.

In a study of some 92 patients suffering from this emerging syndrome, eight developed a full-blown demyelinating CNS disorder (multiple sclerosis). [Authier FJ, Cherin P, et al. Central nervous system disease in patients with macrophagic myofasciitis. Brain 2001; 124: 974-983. ] This included sensory and motor symptoms, visual loss, bladder dysfunction, cerebellar signs (loss of balance and coordination) and cognitive (thinking) and behavioral disorders.

Dr. Gherardi, the French physician who first described the condition in 1998, has collected over 200 proven cases, One third of these develop an autoimmune disease, such as multiple sclerosis. Of critical importance is his finding that even in the absence of obvious autoimmune disease there is evidence of chronic immune stimulation caused by the injected aluminum, known to be a very powerful immune adjuvant.

The reason this is so important is that there is overwhelming evidence that chronic immune activation in the brain (activation of microglial cells in the brain) is a major cause of damage in numerous degenerative brain disorders, from multiple sclerosis to the classic neurodegenerative diseases (Alzheimer's disease, Parkinson's and ALS). In fact, I have presented evidence that chronic immune activation of CNS microglia is a major cause of autism, attention deficit disorder and Gulf War Syndrome.

Dr. Gherardi emphasizes that once the aluminum is injected into the muscle, the immune activation persists for years. In addition, we must consider the effect of the aluminum that travels to the brain itself. Numerous studies have shown harmful effects when aluminum accumulates in the brain. A growing amount of evidence points to high brain aluminum levels as a major contributor to Alzheimer's disease and possibly Parkinson's disease and ALS (Lou Geherig's disease). This may also explain the 10X increase in Alzheimer's disease in those receiving the flu vaccine 5 years in a row. (Dr. Hugh Fudenberg, in press, Journal of Clinical Investigation). It is also interesting to note that a recent study found that aluminum phosphate produced 3X the blood level of aluminum, as did aluminum hydroxide. (Flarend RE, hem SL, et al. In vivo absorption of aluminum-containing vaccine adjuvants using 26 Al. Vaccine 1997; 15: 1314-1318.)

Of course, in this conference, our illustrious experts tell us that there is "no data showing an additive or synergistic effect between mercury and aluminum."

Dr. Rapin expressed her concern over public opinion when this information eventually gets out. She says (page 197), they are going to be captured by the public and we had better make sure that a) "We council them carefully and b) that we pursue this because of the very important public health and public implications of the data." Dr. Johnson adds. "the stakes are very high...". From this how can one conclude anything than the fact that at least these scientists were extremely concerned by what was discovered by this study examining the vaccine safety datalink material? They were obviously terrified that the information would leak out to the public. Stamped in bold letters at the top of each page of the study was the words-"DO NOT COPY OR RELEASE" and "CONFIDENTIAL."

This is not the wording one would expect on a clinical study of vaccine safety; rather you would expect it on top-secret NSA or CIA files. Why was this information being secreted? The answer is obvious-it might endanger the vaccine program and indict the federal regulatory agencies for ignoring this danger for so many years. Our society is littered with millions of children who have been harmed in one degree or another by this vaccine policy. In addition, let us not forget the millions of parents who have had to watch helplessly as their children have been destroyed by this devastating vaccine program.

Dr. Bernier on page 198 says, "the negative findings need to be pinned down and published." Why was he so insistent that the "negative findings" be published? Because he said, "other less responsible parties will treat this as a signal." By that he means, a signal of a problem with thimerosal-containing vaccines. From this, I assume he wants a paper that says only that nothing was found by the study. As we shall see, he gets his wish.

In addition, on page 198, Dr. Rapin notes that a study in California found a 300X increase in autism following the introduction of certain vaccines. She quickly attributes this to better physician recognition. Two things are critical to note at this point. She makes this assertion or better physician recognition without any data at all, just her wishful thinking. If someone pointing out the dangers of vaccines were to do that, she would scream "junk science."

Second, Dr. Weil on page 207, attacks this reasoning when he says, "the number of dose related relationships are linear and statistically significant. You can play with this all you want. They are linear. They are statistically significant." In other words, how can you argue with results that show a strong dose/response relationship between the dose of mercury and neurodevelopmental outcomes? The higher the mercury levels in the children the greater the number of neurological problems.

He continues by saying that the increase in neurobehavioral problems is probably real. He tells them that he works in a school system with special education programs and "I have to say the number of kids getting help in special education is growing nationally and state by state at a rate not seen before. So there is some kind of increase. We can argue about what it is due to." (page 207)

Dr. Johnson seems to be impressed by the findings as well. He says on page 199, "This association leads me to favor a recommendation that infants up to two years old not be immunized with thimerosal containing vaccines if suitable alternative preparations are available." In credibly, he quickly adds "I do not believe the diagnosis justified compensation in the Vaccine Compensation Program at this point." It is interesting to note that one of our experts in attendance is Dr. Vito Caserta, the Chief Officer for the Vaccine Injury Compensation Program.

At this point Dr. Johnson tells the group of his concerns for his own grandchild. He says, (page 200) "Forgive this personal comment, but I got called out at eight o'clock for an emergency call and my daughter-in-law delivered a son by c-section. Our first male in the line of the next generation and I do not want that grandson to get a Thimerosal containing vaccine until we know better what is going on. It will probably take a long time. In the meantime, and I know there are probably implications for this internationally, but in the meanwhile I think I want that grandson to only be given Thimerosal-free vaccines."

So, we have a scientist sitting on this panel which will eventually make policy concerning all of the children in this country, as well as other countries, who is terrified about his new grandson getting a thimerosal-containing vaccine but he is not concerned enough about your child to speak out and try to stop this insanity. He allows a cover-up to take place after this meeting adjourns and remains silent.

It is also interesting to note that he feels the answers will be a long time coming, but in the mean time, his grandson will be protected. The American Academy of Pediatrics, The American Academy of Family Practice, the AMA, CDC and every other organization will endorse these vaccines and proclaim them to be safe as spring water, but Dr, Johnson and some of the others will keep their silence.

It is only during the last day of the conference that we learn that most of the objections concerning the positive relationship between thimerosal-containing vaccines and ADD and ADHA were bogus. For example, Dr. Rapin on page 200 notes that all children in the study were below age 6 and that ADD and ADHD are very difficult to diagnose in pre-schoolers. She also notes that some children were followed for only a short period.

Dr. Stein adds that in fact the average age for diagnosis of ADHD was 4 years and 1 month. A very difficult diagnosis to make and that the guidelines published by the American Academy of Pediatrics limits diagnosis to 6 to 12 year olds. Of course, he was implying that too many were diagnosed as ADHD. Yet, a recent study found that the famous Denmark study that led to the announcement by the Institute of Medicine that there was no relationship between autism and the MMR vaccine, used the same tactic. They cut off the age of follow-up at age six.

It is known that many cases appear after this age group, especially with ADD and ADHD. In fact, most learning problems appear as the child is called on to handle more involved intellectual material. Therefore, the chances are they failed to diagnose a number of cases by stopping the study too early.

Several of the participants tried to imply that autism was a genetic disorder and therefore could have nothing to do with vaccines. Dr. Weil put that to rest with this comment, "We don't see that kind of genetic change in 30 years." In other words, how can we suddenly see a 300% increase in a genetically related disorder over such a short period? It is also known that there are two forms of autism, one that is apparent at birth and one that develops later in childhood. The former has not changed in incidence since statistics have been kept; the other is epidemic.

In one interesting exchange, which ends up being their justification for the view that mercury is of no danger in children vaccinated with vaccines containing thimerosal, involves two studies in children born to mothers consuming high intakes of mercury contaminated fish. One study reported in the journal Neurotoxicology, examined children living in the Republic of Seychelles. In this study, they examined the effect of prenatal exposure to mercury through the mother's consumption of fish high in methylmercury.

A battery of developmental milestone tests were done and no adverse effects were reported in the study reported by Dr. Clarkson and co-workers, the very same person in this conference. He never mentions that a follow-up study of these same children did find a positive correlation between methylmercury exposure and poor performance on a memory test. In a subsequent study of children living on the Faroe Islands exposed to methylmercury, researchers did find impairments of neurodevelopment. This experiment was done by scientist from Japan.

Throughout the remainder of this discussion, Dr. Clarkson and others refer to these two studies. When they are reminded that the Faroe study did find neurological injury to the children, they counter by saying that this was prenatal exposure to mercury and not after birth as would be seen with vaccination. The idea being that prenatally the brain is undergoing neural formation and development making it more vulnerable. As I have mentioned this rapid brain growth and development continues for two years after birth and even at age 6 years the brain is only 80% formed.

Dr. Clarkson keeps referring to the Seychelles study, which demonstrated that the children reached normal neurodevelopmental milestones as shown by a number of tests. Dr Weil points out on page 216 that this tells us little about these children's future brain function. He says, "I have taken a lot of histories of kids who are in trouble in school. The history is that developmental milestones were normal or advanced and they can't read at second grade, they can't write at third grade, they can't do math in the fourth grade and it has no relationship as far as I can tell to the history we get of the developmental milestones. So I think this is a very crude measure of neurodevelopment."

In other words, both of these studies tell us nothing about the actual development of these children's brain function except that they reached the most basic of milestones. To put this another way, your child may be able to stack blocks, recognize shapes and have basic language skills but later in life they could be significantly impaired when it came to higher math, more advanced language skills (comprehension) and ability to compete in a very competitive intellectual environment, like college or advanced schooling. Their future would be limited to the more mundane and intellectually limited jobs.

Post-natal brain development, that is from birth to age six or seven, involves the fine tuning of synaptic connections, dendritic development and pathway refinement, all of which prepare the brain for more complex thinking. These brain elements are very sensitive to toxins and excessive immune stimulation during this period. This is never mentioned in this conference.

In addition, it must be remembered that the children in these two studies were exposed only to methylmercury and not the combined neurotoxic effect of mercury, aluminum and excessive and chronic activation of the brain's immune system (microgia). This is what makes it so incredible, that several of these "vaccinologists" and so-called experts would express doubt about the "biological plausibility" of thimerosal or any vaccine component causing neurodevelopmental problems. The medical literature is exploding with such studies. The biological plausibility is very powerful.

Mercury, for example, even in low concentrations, is known to impair energy production by mitochondrial enzymes. The brain has one of the highest metabolic rates of any organ and impairment of its energy supply, especially during development, can have devastating consequences. In addition, mercury, even oin lower concentrations, is known to damage DNA and impair DNA repair enzymes, which again, plays a vital role in brain development. Mercury is known to impair neurotubule stability, even in very low concentrations. Neurotubules are absolutely essential to normal brain cell function. Mercury activates microglial cells, which increases excitotoxicity and brain free radical production as well as lipid peroxidation, central mechanisms in brain injury. In addition, even in doses below that which can cause obvious cell injury, mercury impairs the glutamate transport system, which in turn triggers excitotoxicity, a central mechanism in autism and other neurological disorders. Ironically, aluminum also paralyzes this system.

On page 228, we see another admission that the government has had no interest in demonstrating the safety of thimerosal-containing vaccines despite over 2000 articles showing harmful effects of mercury. Here we see a reference to the fact that the FDA "has a wonderful facility in Arkansas with hundreds of thousands of animals" available for any study needed to supply these answers on safety. The big question to be asked is -So, why has the government ignored the need for research to answer these questions concerning thimerosal safety. You will recall in the beginning the participants of this conference complained that there were just so few studies or no studies concerning this "problem."

Again, on page 229 Dr, Brent rails about the lawsuit problem. He tells the others that he has been involved in three lawsuits related to vaccine injuries leading to birth defects and concluded "If you want to see junk science, look at those cases...". He then complains about the type of scientists testifying in these cases. He adds, "But the fact is those scientist are out there in the United States." In essence, he labels anyone who opposes the "official policy" on vaccines as a junk scientist. We have seen in the discussion who the "junk scientists" really are.

Knowing that what they have found can cause them a great deal of problems he adds, "The medical/legal findings in this study, causal or not, are horrendous...If an allegation was made that a child's neurobehavioral findings were caused by thimerosal-containing vaccines, you could readily fins a junk scientist who will support the claim with a reasonable degree of certainty." On page 229 he then admits that they are in a bad position because they have no data for their defense. Now, who are the junk scientists?

Is a "real scientist" one who has no data, just wishful thinking and a "feeling" that everything will be all right? Are real scientists the ones who omit recognized experts on the problem in question during a conference because it might endanger the "program"? Or are they the ones who make statements that they don't want their grandson to get thimerosal-containing vaccines until the problem is worked out, but then tell millions of parents that the vaccines are perfectly safe for their children and grandchildren?

Dr. Meyers on page 231 put it this way, "My own concern, and a couple of you said it, there is an association between vaccines and outcomes that worries both parents and pediatricians." He sites other possible connections to vaccine-related neurobehavioral and neurodevelopmental problems including the number of vaccines being given, the types of antigens being used and other vaccine additives.

Dr. Caserta tells the group that he attended the aluminum conference the previous years and learned that often metals could act differently in biological systems than as an ion. This is interesting in the face of the finding that fluoride when combined to aluminum forms a compound that can destroy numerous hippocampal neurons at a concentration of 0.5 ppm in drinking water. It seems that aluminum readily combines with fluoride to form this toxic compound. With over 60% of communities having fluoridated drinking water this becomes a major concern.

It has also been learned that fluroaluminum compounds mimic the phosphate compound and can activate G-proteins. G-proteins play a major role in numerous biological systems, including endocrine, neurotransmitters, and as cellular second messengers. Some of the glutamate receptors are operated by a G-protein mechanism.

Over the next ten to fifteen pages, they discuss how to control this information so that it will not get out and if it does how to control the damage. On page 248 Dr. Clements has this to say:


"But there is now the point at which the research results have to be handled, and even if this committee decides that there is no association and that information gets out, the work has been done and through the freedom of information that will be taken by others and will be used in other ways beyond the control of this group. And I am very concerned about that as I suspect that it is already too late to do anything regardless of any professional body and what they say."

In other words, he wants this information kept not only from the public but also from other scientists and pediatricians until they can be properly counseled. In the next statement he spills the beans as to why he is determined that no outsider get hold of this damaging information. He says,

"My mandate as I sit here in this group is to make sure at the end of the day that 100,000,000 are immunized with DTP, Hepatitis B and if possible Hib, this year, next year and for many years to come, and that will have to be with thimerosal containing vaccines unless a miracle occurs and an alternative is found quickly and is tried and found to be safe."

This is one of the most shocking statements I have ever heard. In essence, he is saying, I don't care if the vaccines are found to be harmful and destroying the development of children's brains, these vaccines will be given now and forever. His only concern by his own admission is to protect the vaccine program even if it is not safe. Dr. Brent refers to this as an "eloquent statement."
On page 253, we again see that these scientists have a double standard when it comes to their children and grandchildren. Dr. Rapin raises the point about a loss of an IQ point caused by thimerosal exposure. She says, "Can we measure the IQ that accurately, that this one little point is relevant?" Then she answers her own question by saying, "Even in my grandchildren, one IQ point I am going to fight about." Yet, they are saying in unison, in essence-TO HELL WITH YOUR CHILDREN- to the rest of America.

It is also interesting that they bring up the history of lead as a neurobehavioral toxin. Dr. Weil noted that the neurotoxicologists and regulatory agencies have lowered the acceptable level from 10 to 5 ug. In fact, some feel that even lower levels are neurotoxic to the developing brain. Before the toxicologists began to look at lead as a brain toxin in children most "experts" assumed it was not toxic even at very high levels. Again, it shows that "experts" can be wrong and it is the public who pays the price.

Dr. Chen on page 256 expresses his concern about this information reaching the public. He remarks, "We have been privileged so far that given the sensitivity of information, we have been able to manage to keep it out of, lets say, less responsible hands..." Dr. Bernier agrees and notes, "This information has been held fairly tightly." Later he calls it "embargoed information" and "very highly protected information."

That they knew the implications of what they had discovered was illustrated by Dr. Chen's statement on page 258. He says, "I think overall there was this aura that we were engaged in something as important as anything else we have ever done. So I think that this was another element to this that made this a special meeting." You may remember, Dr. Weil emphasized that the data analysis left no doubt that there was a strong correlation between neurodevelopmental problems and exposure to thimerosal-containing vaccines. So if they understood the importance of this finding and this was the most important thing they have ever dealt with-why was this being kept from the public? In fact, it gets even worse.

Just so you will not doubt my statement that this audience of experts was not objective, I give you the words of Dr. Walter Orenstein, Director of the National Immunization Program at the CDC, on page 259. He tells the group, "I have seen him (Verstraeten) in audience after audience deal with exceedingly skeptical individuals..." "Exceedingly skeptical individuals" does that sound like objective scientists who wanted to look at the data with a clear mind or were they scientists who were convinced before the meeting was held that there was no danger to children from thimerosal or any other vaccine component?

In one of the closing remarks by Dr. Bernier (page 257) says, "the other thing I was struck by was the science," meaning the science expressed by the attendees of the meeting. Then Dr, Orenstein adds, "I would also like to thank Roger Bernier who pulled off this meeting in rather short notice..." Here is a meeting that has been called one of the most important they have ever dealt with and we learn that it was pulled off on short notice. In addition, we were told that the results of this meeting would lead to eventual vaccine policy.

He then has the nerve to add:


"In a sense this meeting addresses some of the concerns we had last summer when we were trying to make policy in the absence of a careful scientific review. I think this time we have gotten it straight."

Well, I hate to be the one to break the news, but he didn't get it straight. There was little or no science in this meeting; rather it was composed of a lot of haggling and nit picking over epidemiological methodology and statistical minutia in an effort to discredit the data without success. In fact, the so-called mercury experts admitted they had to do some quick homework to refresh their memories and learn something about the subject.
Conclusions

This top secret meeting was held to discuss a study done by Dr. Thomas Verstraeten and his co-workers using Vaccine Safety Datalink data as a project collaboration between the CDC's National Immunization Program (NIP) and four HMOs. The study examined the records of 110,000 children. Within the limits of the data, they did a very through study and found the following:


Exposure to thimerosal-containing vaccines at one month was associated significantly with the misery and unhappiness disorder that was dose related. That is, the higher the child's exposure to thimerosal the higher the incidence of the disorder. This disorder is characterized by a baby that cries uncontrollably and is fretful more so than that see in normal babies.

Found a nearly significant increased risk of ADD with 12.5ug exposure at one month.

With exposure at 3 months, they found an increasing risk of neurodevelopmental disorder with increasing exposure to thimerosal. This was statistically significant. This included speech disorders.

It is important to remember that the control group was not children without thimerosal exposure, but rather those at 12.5ug exposure. This means that there is a significant likelihood that even more neurodevelopmental problems would have been seen had they used a real control population. No one disagreed that these findings were significant and troubling. Yet when the final study was published in the journal Pediatrics Dr. Verstraeten and co-workers reported no consistent associations were found between thimerosal-containing vaccine exposure and neurodevelopmental problems. In addition, he list himself as an employee of the CDC, not disclosing the fact that at the time the article was accepted, he worked for GlaxoSmithKline, a vaccine manufacturing company.
So how did they do this bit of prestidigitation? They simply added another HMO to the data, the Harvard Pilgrimage. Congressman Dave Weldon noted in his letter to the CDC Director that this HMO had been in receivership by the state of Massachusetts because its records were in shambles. Yet, this study was able to make the embarrassing data from his previous study disappear. Attempts by Congressman Weldon to force the CDC to release the data to an independent researcher, Dr. Mark Geier, a researcher with impeccable credentials and widely published in peer-reviewed journals, have failed repeatedly.

It is obvious that a massive cover-up is in progress, as we have seen with so many other scandals-fluoride, food-based excitotoxins, pesticides, aluminum and now vaccines. I would caution those critical of the present vaccine policy not to put all their eggs in one basket, that is, with thimerosal as being the main culprit. There is no question that it plays a major role, but there are other factors that are also critical, including aluminum, fluoroaluminum complexes, and chronic immune activation of brain microglia.

In fact, excessive, chronic microglial activation can explain many of the effects of excessive vaccine exposure as I point out in two recently published articles. One property of both aluminum and mercury is microglial activation. With chronic microglial activation large concentrations of excitotoxins are released as well as neurotoxic cytokines. These have been shown to destroy synaptic connections, dendrites and cause abnormal pathway development in the developing brain as well as adult brain.

In essence, too many vaccines are being given to children during the brain's most rapid growth period. Known toxic metals are beings used in the vaccines that interfere with brain metabolism, antioxidant enzymes, damage DNA and DNA repair enzymes and trigger excitotoxicity. Removing the mercury will help but will not solve the problem because overactivation of the brain's immune system will cause varying degrees of neurological damage to the highly-vulnerable developing brain.


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Kawase T, Ishikawa I, Orikasa M, Suzuki A. An assessment of the impact of thimerosal on childhood neurodevelopmental disorders. Geier DA, Geier MR. J Biochem (Tokyo). 1989 Jul; 106(1): 8-10. Aluminum enhances the stimulatory effect of NaF on prostaglandin E2 synthesis in a clonal osteoblast-like cell line, MOB 3-4, in vitro. Pediatr Rehabil. 2003 Apr-Jun;6(2):97-102.

Geier MR, Geier DA. Thimerosal in childhood vaccines, neurodevelopmental disorders, and heart disease in the United States. J Amer Physc Surg 8: 6-11, 2003.

Allen JW, Shanker G, Tan KH, Aschner M. The consequences of methylmercury exposure on interactive functions between astrocytes and neurons. Neurotoxicology 23: 755-759, 2002.

Hansen JC, Reske-Nielsen E, et al. Distribution of dietary mercury in a dog. Quantitation and localization of total mercury in organs and central nervous system. Sci Total Environ 78: 23-43, 1989.

Zanoli P, Cannazza G, Baraldi M. Prenatal exposure to methyl mercury in rats: focus on changes in kyrenine pathway. Brain Res Bull 55: 235-238, 2001.

Olivieri G, Brack C, et al. Mercury induces cell cytotoxicity and oxidative stress and increases beta-amyloid secretion and tau phosphorylation in SHY5Y neuroblastoma cells. J Neurochem 74: 231-236, 2000.

Juarez BI, Mattinez M, et al. Methylmercury increases glutamate extracellular levels in frontal cortex of awake rats. Neurotoxicology and Teratology 24: 767-771, 2002.

Geier DA, Geier MR. An assessment of the impact of thimerosal on childhood neurodevelopmental disorders. Pediatric Rehabil 6: 97-102, 2003.

Geier DA, Geier MR. A comparative evaluation of the effects of MMR immunization and mercury doses from thimerosal-containing childhood vaccines on the population prevalence of autism. Med Sci Monit 10: P133-139, 2004.

Baskin DS, Ngo H, Didenko VV. Thimerosal indices DNA breaks, caspase-3 activation, membrane damage, and cell death in cultured human neurons and fibroblast. Toxicol Sci 74: 361-368, 2003.

Pichichero ME, et al. Mercury concentrations and metabolism in infants receiving vaccines containing thimerosal: a descriptive study. Lancet 360: 1737-1741, 2002.

Murata K, Dakeishi M. Impact of prenatal methylmercury exposure on child neurodevelopment in the Faroe Islands. Nippon Eiseigaku Zasshi 57: 564-570, 2002.

Davidson PW, Myers GJ, et al (Clarkson TW-member of panel) Effects of prenatal and postnatal exposure from fish consumption on neurodevelopment: outcomes at 66 months of age in the Seychelles Child Development Study. JAMA 280: 701-707, 1998.

Palumbo DR, Cox C, et al. (ClarksonTW) Association between prenatal exposure to methylmercury and cognitive functioning in Seychellois children: a reanalysis of the McCarthy Scales of Children's Ability from the main cohort study. Environ Res 84: 81-88, 2000.

Hornig M, Chian D, Lipkin WI. Neurotoxic effects of postnatal thimerosal are mouse strain dependent. Mol Psychiatry (In press).

Ueha-Ishibashi T, et al. Property of thimerosal-induced decrease in cellular content of gluatathione in rat thymocytes: a flow cytometric study with 5-chloromethylfluorescein. Toxicol in Vitro 18: 563-569, 2004.

Ueha-Ishibaschi T, et al. Effect of thimerosal, a preservative in vaccines, on intracellular Ca+2 concentration of ra cerebellar neurons. Toxicology 195: 77-84, 2004.

Havarinasab S, Lambertsson L, et al. Dose-response study of thimerosal-induced murine systemic autoimmunity. Toxicol Appl Pharmacol 194: 169-179, 2004.

Verstraeten T, Davis RL, DeStefano F, et al. Safety of thimerosal-containing vaccines: a two-phase study of computerized health maintenance organization databases. Pediatrics 112: 1039-1048, 2003. (This is the published study that was discussed in the conference. Her the damaging data is erased and the public is told the thimerosal-containing vaccines are perfectly safe. In this paper Dr. Verstraeten identified himself as working for the CDC, but in fact he is working for GlaxoSmithKline. The editors of the journal Pediatrics should have been willing to disclose this information once it was brought to their attention but they would not.).

Aluminum References

Murayama H, Shin RW, Higuchi J, Shibuya S, Muramoto T, Kitamoto T. Interaction of aluminum with PHFtau in Alzheimer's disease neurofibrillary degeneration evidenced by desferrioxamine-assisted chelating autoclave method.Am J Pathol. 1999 Sep;155(3):877-85.

Shin RW, Kruck TP, Murayama H, Kitamoto T. A novel trivalent cation chelator Feralex dissociates binding of aluminum and iron associated with hyperphosphorylated tau of Alzheimer's disease. Brain Res. 2003 Jan 24;961(1):139-46.

Li W, Ma KK, Sun W, Paudel HK. Phosphorylation sensitizes microtubule-associated protein tau to Al(3+)-induced aggregation. Neurochem Res. 1998 Dec;23(12):1467-76.

Singer SM, Chambers CB, Newfry GA, Norlund MA, Muma NA. Tau in aluminum-induced neurofibrillary tangles. Neurotoxicology. 1997;18(1):63-76.

Toda S, Yase Y. Effect of aluminum on iron-induced lipid peroxidation and protein oxidative modification of mouse brain homogenate. Biol Trace Elem Res. 1998 Feb;61(2):207-17.

Sayre LM, Perry G, Harris PL, Liu Y, Schubert KA, Smith MA. In situ oxidative catalysis by neurofibrillary tangles and senile plaques in Alzheimer's disease: a central role for bound transition metals. J Neurochem. 2000 Jan;74(1):270-9.

Xie CX, Yokel RA. Aluminum facilitation of iron-mediated lipid peroxidation is dependent on substrate, pH and aluminum and iron concentrations. Arch Biochem Biophys. 1996 Mar 15;327(2):222-6.

Kawase T, Ishikawa I, Orikasa M, Suzuki A. Aluminum enhances the stimulatory effect of NaF on prostaglandin E2 synthesis in a clonal osteoblast-like cell line, MOB 3-4, in vitro. J Biochem (Tokyo). 1989 Jul; 106(1): 8-10.

Jope RS. Modulation of phosphoinositide hydrolysis by NaF and aluminum in rat cortical slices. J Neurochem. 1988 Dec; 51(6): 1731-6.

Blair HC, Finch JL, Avioli R, Crouch EC, Slatopolsky E, Teitelbaum SL. Micromolar aluminum levels reduce 3H-thymidine incorporation by cell line UMR 106-01. Kidney Int. 1989 May; 35(5): 1119-25.

Shainkin-Kestenbaum R, Adler AJ, Berlyne GM, Caruso C. Effect of aluminium on superoxide dismutase. Clin Sci (Lond). 1989 Nov; 77(5): 463-6.

Kawase T, Orikasa M, Suzuki A. Aluminofluoride- and epidermal growth factor-stimulated DNA synthesis in MOB 3-4-F2 cells. Pharmacol Toxicol. 1991 Nov; 69(5): 330-7.

Gomes MG, Moreira CA, Mill JG, Massaroni L, Oliveira EM, Stefanon I, Vassallo DV. Effects of aluminum on the mechanical and electrical activity of the Langendorff-perfused rat heart. Braz J Med Biol Res. 1994 Jan; 27(1): 95-100.

Jope RS. Modulation of phosphoinositide hydrolysis by NaF and aluminum in rat cortical slices. J Neurochem. 1988 Dec; 51(6): 1731-6.

Husaini Y, Rai LC, Mallick N. Impact of aluminium, fluoride and fluoroaluminate complex on ATPase activity of Nostoc linckia and Chlorella vulgaris. Biometals. 1996 Jul; 9(3): 277-83.

Blair HC, Finch JL, Avioli R, Crouch EC, Slatopolsky E, Teitelbaum SL. Micromolar aluminum levels reduce 3H-thymidine incorporation by cell line UMR 106-01. Kidney Int. 1989 May; 35(5): 1119-25.

Lai JC, Lim L, Davison AN. Effects of Cd2+, Mn2+, and Al3+ on rat brain synaptosomal uptake of noradrenaline and serotonin. J Inorg Biochem. 1982 Nov; 17(3): 215-25.

Shainkin-Kestenbaum R, Adler AJ, Berlyne GM, Caruso C. Effect of aluminium on superoxide dismutase. Clin Sci (Lond). 1989 Nov; 77(5): 463-6.

Department of Health and Human Services National Vaccine Program Office Presents: Workshop on Aluminum in Vaccines. Caribe Hilton International Hotel, San Juan, Puerto Rico: Jointly sponsored by: task Force for Child Survival and Development. May 12, 200.

Varner JA, Jenson KF, Harvath W, Isaacson RL. Chronic administration of aliminum-fluoride or sodium-fluoride to rats in drinking water: alterations in neuronal and cerebrovascular integrity. Brain Res 784: 284-298, 1998.

Strunecka A, Pataocka J. Aluminofluoride complexes: new phosphate analogues for laboratory investigations and potential danger for living organisms. http://www.fluoridation.com/brain3.htm

Candura SM, Castildi AF, et al. Interaction of aluminum ions with phosphoinositide metabolism in rat cerebral cortical membranes. Life Sci 49: 1245-1252, 1991.

Publicover SJ. Brief exposure to the G-protein activator NaF/ AlCl3 induces prolonged enhancement of synaptic transmission in area of rat hippocampal slices. Expl Brain Res 84: 680-684, 1991.

Brenner A. Macrophagic myofascitiitis: a summery of Dr. Gherardi's presentations. Vaccine 20�Supp 3): S5-6, 2002.

Lacson AG, D'Cruz CA, et al. Aluminum phagocytosis in quadriceps muscle following vaccination in children: relationship to macrophagic myofasciitis. Pediatr Dev Pathol 5: 151-158, 2002.

Flarend RE, Hem SL, et al. In vivo absorption of aluminum-containing vaccine adjuvants using 26 Al. Vaccine 15: 131401318, 1997.

Authier FJ Cherin P, et al. Central nervous system disease in patients with macrophagic myofasciitis. Brain 124: 974-983, 2001.

Gherardi RK. Lessons from macrophagic myofasciitis: towards definition of a vaccine adjuvant-related syndrome. Rev Neurol (Paris) 159: 162-164, 2003.

Bergfors E, Trollfors B, Inerot A. Unexpectantly high incidence of persistent itching and delayed hypersensitivity to aluminum in children after the used of absorbed vaccines from a single manufacturer. Vaccine 22: 64-69, 2003.

Deloncle R, Fauconneau B, et al. Aluminum L-glutamate complexes in rat brain cortex: in vivo prevention of aluminum deposit by magnesium D-aspartate. Brain Res 946: 247-252, 2002.

Mundy WR, Freudenrich TM, Kodavanti PR. Aluminum potentates glutamate-induced calcium accumulation and iron-induced oxygen free radical formation in primary neuronal cultures. Mol Chem Neuropathol 32: 41-57, 1997.

References Concerning Lead

Naatala JT, Loikkanen JJ, et al. Lead amplifies glutamate-induced oxidative stress. Free Radical Biology Medicine 19: 689-693, 1995.

Morgan RE, Garavan H, et al. Early lead exposure produces lasting changes in sustained attention, response initiation, and reactivity to errors. Neurotoxicology and Teratology 23: 519-531, 2001.

Needleman HL, McFarland C, et al. Bone lead levels in adjudicated delinquents: A case control study. Neurotoxicology and Teratology 24: 711-717, 2002.

Dietrich KN, Ris MD, et al. Early exposure to lead and juvenile delinquency. Neurotoxicology and Teratology 23: 511-518, 2001.

Dr. Russell Blaylock, M.D. References

Blaylock R. Interaction of cytokines, excitotoxins, and reactive nitrogen and oxygen species in autism spectrum disorders. J. Amer Nutr Assoc 6: 21-35, 2003.

Blaylock RL. The central role of excitotoxicity in autism spectrum disorders. J Amer Nutra Assoc 6: 7-19, 2003.

Blaylock RL. Chronic microglial activation and excitotoxicity secondary to excessive immune stimulation: possible factors in Gulf War Syndrome and autism. J Amer Phys Surg 9: 46-51, 2004.

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1991 Memo Warned of Mercury in Children's Vaccines

1991 Memo Warned of Mercury in Children's Vaccines

Los Angeles Times
February 8, 2005
By Myron Levin, Times Staff Writer

A memo from the drug maker Merck & Co. shows that, nearly a decade before the first public disclosure, senior executives were concerned that infants were getting an elevated dose of mercury in vaccinations containing a widely used sterilizing agent.

The March 1991 memo, obtained by The Times, said that 6-month-old children who received their shots on schedule would get a mercury dose up to 87 times higher than guidelines for the maximum daily consumption of mercury from fish.

"When viewed in this way, the mercury load appears rather large," said the memo from Dr. Maurice R. Hilleman, an internationally renowned vaccinologist. It was written to the president of Merck's vaccine division.

The memo was prepared at a time when U.S. health authorities were aggressively expanding their immunization schedule by adding five new shots for children in their first six months. Many of these shots, as well as some previously included on the vaccine schedule, contained thimerosal, an antibacterial compound that is nearly 50% ethyl mercury, a neurotoxin.

Federal health officials disclosed for the first time in 1999 that many infants were being exposed to mercury above health guidelines through routine vaccinations. The announcement followed a review by the U.S. Food and Drug Administration that was described at the time as a first effort to assess the cumulative mercury dose.

But the Merck memo shows that at least one major manufacturer was aware of the concern much earlier.

"The key issue is whether thimerosal, in the amount given with the vaccine, does or does not constitute a safety hazard," the memo said. "However, perception of hazard may be equally important."

Merck officials would not discuss the contents of the memo, citing pending litigation.

Separately, the drug giant is trying to fend off a legal onslaught over Vioxx, the popular painkiller it introduced in 1999. The company, based in Whitehouse Station, N.J., faces hundreds of lawsuits claiming that the drug caused heart problems and that Merck concealed the risks. Merck, which in September pulled Vioxx off the market, has denied the allegations.

The legacy of thimerosal, meanwhile, also is causing problems for Merck and other drug companies.

More than 4,200 claims have been filed in a special federal tribunal, the Vaccine Injury Compensation Program, by parents asserting that their children suffered autism or other neurodevelopmental disorders from mercury in vaccines. A handful of similar claims are awaiting trial in civil courts. The plaintiffs cite various scientific studies that they say prove the dangers of thimerosal, including at the levels found in vaccines.

Thimerosal has been largely removed from pediatric vaccines in recent years in what health officials have described as a precautionary measure. (This has been accomplished as drug makers have voluntarily switched from multi-dose vials of vaccine, which require a chemical preservative like thimerosal, to single-dose containers.)

In September, Gov. Arnold Schwarzenegger signed legislation prohibiting vaccines with more than trace amounts of thimerosal from being given to babies and pregnant women. Iowa has a similar ban.

For their part, Merck and other vaccine makers, along with many government health officials and scientists, say there is no credible evidence of harm from the amounts of mercury once widely present in kids' shots. They cite a report in May by a committee of the national Institute of Medicine concluding that the evidence "favors rejection of a causal relationship" between vaccines and autism.

The seven-page Merck memo was provided to The Times by James A. Moody, a Washington lawyer who works with parent groups on vaccine safety issues. He said he obtained it from a whistle-blower whom he would not name.

The memo provides the "first hard evidence that the companies knew — or at least Merck knew — that the children were getting significantly more mercury" than the generally accepted dose, the lawyer said.

He also provided a copy to attorneys for Vera Easter, a Texas woman who blames thimerosal for the condition of her 7-year-old son, Jordan, who is autistic and mentally retarded. The Easter lawsuit is pending in U.S. District Court for the Eastern District of Texas. The defendants include Merck; rival vaccine makers GlaxoSmithKline, Aventis Pasteur Inc. and Wyeth; and thimerosal developer Eli Lilly & Co.

Easter's lawyer, Andy Waters, described the memo as "incredibly damning and incredibly significant." After receiving it in the fall, he confronted Merck lawyers about why he hadn't seen it earlier.

In a letter to Waters in October, Merck attorneys said they had in fact made available 32 boxes of records, but that the copying service hired by the plaintiffs for some reason had failed to copy several of the boxes — including the one with the Hilleman memo.

"The memo," said company spokeswoman Mary Elizabeth Blake, "was produced voluntarily by Merck in the ordinary course of discovery proceedings."

Hilleman is a former senior vice president of Merck who developed numerous vaccines for the company. A 1999 profile in the Philadelphia Inquirer said that "it is no exaggeration to assert, as many scientists do, that Maurice Hilleman has saved more lives than any other living scientist."

Hilleman, 85, currently director of the Merck Institute for Vaccinology, had officially retired and was a consultant to Merck when he wrote the '91 memo. He declined to be interviewed.

The memo was sent to Dr. Gordon Douglas, then head of Merck's vaccine division and now a consultant for the Vaccine Research Center at the National Institutes of Health. Douglas also declined to comment.

The memo stated that regulators in several countries had raised concerns about thimerosal, including in Sweden, where the chemical was being removed from vaccines.

"The public awareness has been raised by the sequential wave of experiences in Sweden including mercury exposure from additives, fish, contaminated air, bird deaths from eating mercury-treated seed grains, dental amalgam leakage, mercury allergy, etc.," the memo said.

It noted that Sweden had set a daily maximum allowance of mercury from fish of 30 micrograms for a 160-pound adult, roughly the same guideline used by the FDA. Adjusting for the body weight of infants, Hilleman calculated that babies who received their shots on schedule could get 87 times the mercury allowance.

The Swedish and FDA guidelines work out to about four-tenths of a microgram of mercury per kilogram of body weight. A stricter standard of one-tenth of a microgram per kilogram has been adopted by the Environmental Protection Agency and endorsed by the National Research Council.

These standards are based on methyl mercury, the type found in fish and airborne emissions from power plants. Though toxic, the ethyl mercury in thimerosal may be less hazardous than methyl mercury, some scientists say, because it is more quickly purged from the body.

"It appears essentially impossible, based on current information, to ascertain whether thimerosal in vaccines constitutes or does not constitute a significant addition to the normal daily input of mercury from diverse sources," the memo said.

"It is reasonable to conclude" that it should be eliminated where possible, he said, "especially where use in infants and young children is anticipated."

In the U.S., however, thimerosal continued to be added throughout the '90s to a number of widely used pediatric vaccines for hepatitis B, bacterial meningitis, diphtheria, whooping cough and tetanus.

It was added to multi-dose vials of vaccine to prevent contamination from repeated insertion of needles to extract the medicine. It was not needed in single-dose vials, but most doctors and clinics preferred to order vaccine in multi-dose containers because of the lower cost and easier storage.

The Hilleman memo said that unlike regulators in Sweden and some other countries, "the U.S. Food and Drug Administration … does not have this concern for thimerosal."

A turning point came in 1997 when Congress passed a bill ordering an FDA review of mercury ingredients in food and drugs.

Completed in 1999, the review revealed the high level of mercury exposure from pediatric vaccines and raised a furor. In e-mails later released at a congressional hearing, an FDA official said health authorities could be criticized for "being 'asleep at the switch' for decades by allowing a potentially hazardous compound to remain in many childhood vaccines, and not forcing manufacturers to exclude it from new products."

It would not have taken "rocket science" to add up the amount of exposure as the prescribed number of shots was increasing, one of the e-mails said.

While asserting that there was no proof of harm, the U.S. Public Health Service in July 1999 called on manufacturers to go mercury-free by switching to single-dose vials. Soon after, Merck introduced a mercury-free version of its hepatitis B vaccine, replacing the only thimerosal-containing vaccine it was still marketing at the time, a company spokesman said.

By 2002, thimerosal had been eliminated or reduced to trace levels in nearly all childhood vaccines. One exception is the pediatric flu vaccine made by Aventis and still sold mainly in multi-dose vials.

WHAT YOU NEED TO KNOW ABOUT VACCINE LAWS IN AMERICA

WHAT YOU NEED TO KNOW ABOUT
VACCINE LAWS IN AMERICA
The National Vaccine Information Center
(NVIC) is a non-profit charity founded in 1982
by parents of vaccine injured children to
prevent vaccine injuries and deaths through
public education and defend the ethical
principle of informed consent to medical
risk-taking.
NVIC and Mercola.com are partners in presenting
you with accurate information about
heath and vaccination and encouraging you
to stand up for your right to make informed,
voluntary vaccination decisions.
I am joining with Barbara Loe Fisher, cofounder
and president of the National Vaccine
Information Center, to urge you to remember three basic facts when you are
taking control of your health by making vaccine and other health care choices for
yourself or your child:
1
2
INFORMED CONSENT IS A HUMAN RIGHT
The right to voluntary, informed consent to a medical intervention, including
use of a pharmaceutical product such as a vaccine that can injure
or kill you or your child, is a human right.
While the State may have the legal authority to mandate use of vaccines,
nobody has the moral authority to FORCE you to get vaccinated or vaccinate
your child without your voluntary, informed consent.
VACCINE LAWS HAVE EXEMPTIONS
In 1905, the U.S. Supreme Court affirmed the legal authority of state
governments to pass laws requiring citizens residing in the state to use
certain vaccines.
Today, all 50 states have enacted vaccine laws that require proof of vaccination
for children to attend daycare, elementary, junior and high school
and college.
Vaccine requirements vary from state to state and all 50 states allow a
medical exemption to vaccination; 48 states allow a religious exemption
1
to vaccination; and 18 states allow a personal, philosophical or conscientious
belief exemption to vaccination.
To look at a map of the U.S. and find out what your state vaccine law says
and which exemptions you may take and how to take them, click here.
3 FREEDOM IS NOT FREE: BECOME A VACCINE CHOICE ADVOCATE
Many state governments now require nearly three dozen doses of more
than a dozen vaccines to attend school. Medical and religious exemptions
are becoming harder to get and exemptions for reasons of conscience
are under attack by proponents of forced vaccination.
The National Vaccine Information Center is working with citizens in all
states to expand or protect legal exemptions to vaccination. To register
for NVIC’s Advocacy Portal and take action in YOUR state, click here.
SIX PRINCIPLES FOR PROTECTING
VACCINE CHOICES
FIRST PRINCIPLE: It’s Your CHOICE
When exercising your right to voluntary, informed consent to vaccination for
yourself or your child, remember that state vaccine laws contain:
(1) Legal requirements which school and health officials are responsible for enforcing;
and
(2) Legal exemptions which you have the legal right to choose to exercise. (Public
schools must al low vaccine exemptions outlined outlined in state vaccine laws,
but private religious or other non-state operated schools may reject vaccine
exemptions.)
Most state vaccine laws do not allow unvaccinated students with vaccine exemptions
to attend school during confirmed outbreaks of certain infectious diseases
for defined periods of time.
Remember: Nobody has the moral authority to force you or your child to be
injected with a vaccine without your voluntary, informed consent and you have
the legal right to exercise exemptions to vaccination according to the laws in your
state.
2
SECOND PRINCIPLE: You Have the Right to KNOW
You have the legal right to know the risks and complications of vaccines BEFORE
you make the choice of whether or not to allow your child to be vaccinated.
The National Childhood Vaccine Injury Act of 1986 directed all doctors and
other vaccine providers to give parents written information about vaccines BEFORE
children are vaccinated.
Remember: All vaccines and other pharmaceutical
products carry a risk of injury or death and those
risks can be greater for some than others.
Never agree to use a vaccine, drug or other product
without fully informing yourself about ALL risks.
The product information insert, which drug companies
by law must include with every vial of vaccine
provided to public health clinics and private doctors’
offices, includes a description of the vaccine’s
reported reactions and precautions.
You can ask for a copy of that vaccine information
insert from your doctor or state health department
or go to www.NVIC.org or www.NVICadvocacy.org
for copies of vaccine product information inserts.
THIRD PRINCIPLE: Be INFORMED and Prepared
Knowledge is power. Arm yourself with accurate information about vaccination
and health. Do your own research and talk to one or more trusted health care
professionals before you make any health care decision.
Become an educated consumer and you will be empowered to defend your right
to freely make voluntary choices about health, including vaccination, for yourself
and your children. Visit the National Vaccine Information Center website at www.
NVIC.org or www.NVICadvocacy.org for more information about vaccines and
health.
Remember: If you arm yourself with accurate information about vaccines and
health, you will be prepared to intelligently and rationally discuss your vaccine
choices with your family, friends, colleagues, doctors, elected officials and others
in your community.
3
FOURTH PRINCIPLE: Take RESPONSIBILITY for Your Words and Actions
When you are standing up for
your right to know, and freedom to
choose, whether or not to vaccinate
yourself or your child, how you go
about exercising your rights will
determine whether or not you will
succeed.
In your contact with doctors, school
or government health officials,
remain calm but politely firm when
explaining and defending the vaccine choice you have made.
If you are treated with disrespect or are harassed in any way by a doctor or
government official, do not engage in an unproductive argument. You may want
to contact an attorney, your elected state representatives or local media if you or
your child are threatened.
To publicly post a report of harassment for your vaccine choice, click here.
Remember: Treat others as you want to be treated, even if you are being attacked
or harassed for the vaccine choice you have made.
Protect yourself and your family by seeking legal or other expert counsel, if necessary.
Serve as an example for others in your community whenever you defend your
right to exercise voluntary, informed consent to vaccination, including the right to
decline to use one or more vaccines for yourself or your child.
FIFTH PRINCIPLE: Keep WRITTEN Records
Be sure to ask your doctor for copies of your medical records or your child’s medical
records, including recorded information about vaccinations and illnesses. Under
the National Childhood Vaccine Injury Act of 1986, doctors and other vaccine
providers are required by federal law to:
write down any serious health problems that occur after
vaccination in a child’s permanent medical record;
keep a permanent record of all vaccines given, including the
manufacturer’s name and lot number; and
Report serious health problems, hospitalizations injuries and deaths
that occur after vaccination to the federal Vaccine Adverse Events
Reporting System (VAERS). (If your doctor won’t report, you have the
4
SIXTH PRINCIPLE: Be COURAGEOUS
It is not easy to stand up for the right to make informed, voluntary choices about
vaccination when public health officials, the pharmaceutical industry and many
medical doctors are putting pressure on all Americans, especially parents, to use
every government recommended vaccine.
The fact that the numbers of doses of government mandated vaccines have tripled
in the past quarter century, while the numbers of chronically ill and disabled
children have also tripled, offers an opportunity to have a long overdue public
conversation about the effects of vaccination on individual and public health.
Remember: Freedom of thought and exercise of free speech is protected under
the US Constitution.
You have the right to talk privately and publicly about any concerns you have
about vaccine necessity, safety and effectiveness, and to work with your elected
officials to modify the vaccine laws in your state.
Become an engaged, courageous citizen activist and protect your right to make
vaccine choices.
right to make a vaccine reaction report to VAERS).
Remember: It is wise to keep written records of your interactions with doctors,
school and health officials that involve vaccine choices you make, as well as
Medical Exemptions: All 50 states allow
medical exemption to vaccination.
Medical exemptions to vaccination must be
written by a medical doctor (M.D.) or doctor of
osteopathy (D.O.) and are usually reviewed annually
by school or state health officials.
Since 1986, the Centers for Disease Control (CDC)
and American Academy of Pediatrics (AAP) have
eliminated most officially recognized medical reasons for withholding vaccination
(contraindications) so that almost no medical condition qualifies for a medical
exemption to vaccination.
In most states, school or state public health officials can question or even deny a
VACCINATION AND U.S. LAW
A BRIEF SUMMARY
5
medical exemption to vaccination written by a doctor if it does not strictly conform
to CDC and AAP contraindication guidelines.
The National Vaccine Information Center is committed to working with citizens
who want to change vaccine laws to prevent state school or health officials from
questioning or denying a medical exemption to vaccination written by a doctor,
nurse practitioner or physician’s assistant. If you want to take action in your state
to modify the medical exemption to vaccination, register for the NVIC Advocacy
Portal at www.NVICadvocacy.org
Religious Exemptions: All but two states (West Virginia and Mississippi)
allow religious exemption to vaccination.
These exemptions are worded differently in different states and require different
forms of written documentation that must be submitted to state governments
supporting a sincerely held religious belief opposing vaccination.
Some states require a notarized affidavit or letter from a spiritual advisor attesting
to the sincerity of a person’s religious beliefs about vaccination. The religious
exemption is under attack and, in some states like New York, parents are being
grilled about the sincerity of their religious beliefs by state officials and denied
religious exemptions to vaccination so their partially or completely unvaccinated
children cannot attend public schools.
The National Vaccine Information Center is committed to working with citizens,
who want to protect their right to religious exemption to vaccination, to add or
re-write the religious exemption in state vaccine laws. If you would like to work in
your state to protect or strengthen the religious exemption to vaccination, register
for the NVIC Advocacy Portal at www.NVICadvocacy.org
Conscientious Belief Exemptions: 18 states allow conscientious, personal
or philosophical belief exemption to vaccination. These states come the
closest to protecting a citizen’s right to exercise voluntary, informed consent to
vaccination in America. They are: Arizona, California, Colorado, Idaho, Louisiana,
Maine, Michigan, Minnesota, New Mexico, North Dakota, Ohio, Oklahoma, Rhode
Island, Texas, Utah, Vermont, Washington and Wisconsin
This exemption, like the religious exemption, is under attack by forced vaccination
proponents who want to eliminate non-medical exemptions to vaccination in
America.
The National Vaccine Information Center is committed to working with citizens
who want to protect or add conscientious belief exemption in state vaccine laws.
If you want to take action in your state to protect or add the conscientious belief
exemption to vaccine laws in your state, register for the NVIC Advocacy Portal at
www.NVICadvocacy.org
6
Vaccine Exemptions for Military Personnel: All branches of the U.S.
Armed Services provide medical and
religious exemptions to vaccination, but
those exemptions must be first declared
before enlistment in the military.
If a military recruit does not clearly state a
medical or religious objection to vaccination
BEFORE joining the military, he or she
gives up the right to object to vaccination
Other Vaccine Exemption Issues: Vaccine choices also can affect adoption,
immigration, child custody arrangements during divorce proceedings,
eligibility for health insurance and government entitlement programs, and medical
care.
Children adopted from foreign countries as well as in the U.S. may be required by
US law and adoption agencies to receive certain government mandated vaccines.
Immigration laws also contain vaccine requirement provisions.
In cases of divorce, one parent may attempt to gain full custody of a minor child
by using the vaccine choice issue as leverage.
Some families have been dropped from medical insurance plans or barred from
eligibility for government funded medical care and food supplement programs if
children are not given all government recommended vaccines.
Increasingly, pediatricians are refusing to treat children who are not fully vaccinated
and, in some instances, medical personnel in hospital emergency rooms and
physicians’ offices have reported parents to state child social services agencies
for child medical neglect for refusing to vaccinate their children. In these circumstances,
you may need to consult to protect informed consent rights.
LEGAL OPTION
The National Childhood Vaccine Injury Act of 1986 was passed by Congress to
protect vaccine manufacturers and vaccine providers from liability for vaccine
injuries and deaths in civil court.
If a child is injured by a government recommended or mandated vaccine, the
child must sue the Secretary of Health for damages under the Act in the U.S. Court
of Claims in Washington, D.C.
If the vaccine injured child is turned down for federal compensation or offered
too little to provide for the child’s lifetime care, a lawsuit may be filed in civil court
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against a vaccine manufacturer or negligent doctor with certain restrictions.
By 2010, more than $2 billion had been awarded to vaccine victims for brain
inflammation and immune system damage leading to permanent injury or death,
even though two out of three children are turned away for federal compensation.
When you or your child is injured
by a vaccine, the risks are 100 percent,
and you will be left to deal
with the consequences.
Those who make and give vaccines
are protected from liability
in civil court, and federal vaccine
injury compensation is very difficult
to get.
There is no guarantee that a vaccine will, in fact, protect against an infectious
disease or that exposure to an infectious disease will cause a complication,
injury or death. Good health is about so much more than vaccination
and preventing experience with infectious disease.
Vaccines are pharmaceutical products that carry a risk of injury or death
that is greater for some than others. The right to informed consent to medical
risk-taking is a human right.
Empowering ourselves with information and taking responsible action to
protect the right to exercise voluntary, informed consent to vaccination
in America is one of the most important actions we can take as citizens to
protect our freedom.
Don’t let anyone force you or your child to take a vaccine without your
voluntary, informed consent.
If a doctor denies you or your child medical care because you want to make
vaccine choices, find another doctor.
If a doctor threatens you, or if a government official denies a medical or
religious exemption that you have legally filed, find an attorney to help you.
If you don’t like the vaccine laws in your state, contact your elected officials
and work to change them.
Together, we can educate the public and reform vaccine laws in America
to protect the right to make informed, voluntary vaccination decisions for
ourselves and our children.
THE BOTTOM LINE
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FOR MORE INFORMATION:
On the website of the National Vaccine Information Center under Diseases
& Vaccines there is information and links to resources that will educate you
about infectious diseases and vaccines.
Vaccines.Mercola.com
State Laws & Vaccine Exemption Information
Become a Vaccine Choice Advocate in your state to protect vaccine exemptions.
Register for NVIC’s Advocacy Portal at www.NVICadvocacy.org
If you have been harassed for your vaccine choices, make a report here
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