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.
References For This Article
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