Autism is vaccine related - Dr R Blaylock - MD

[Guest guest]

The Danger of Excessive Vaccination During Brain Development: The Case for a

Link to Autism Spectrum Disorders

 

 

 

Russell L. Blaylock, M.D.

 

http://web.mac.com/rblaylock/Russell_Blaylock_M.D./Information/Entries/2008/3/12\

_Vaccines%2C_Neurodevelopment_and_Autism_Spectrum_Disorders.html

 

 

In 1976, children received 10 vaccines before attending school. Today they will

receive over 36 injections. The American Academy of Pediatrics and the Center

for Disease Control assured parents that it was safe to not only give these

vaccines, but that they could be given at one time with complete safety. Is this

true? Or are we being lied to on a grand scale?

 

The medical establishment has created a set of terms, which they use constantly

to boost their egos and firm up their authority as the unique holders of medical

wisdom–the mantra is “evidence-based medicineâ€, as if everything outside

their anointing touch is bogus and suspect. A careful examination of many of the

accepted treatments reveals that most have little or no scientific

“evidence-based†data to support it. One often repeated study found that

almost 80% of medical practice had no scientific backing.

 

This is not to say that medical practice should be purely based on pure and

applied science, as understood in the fields of physics and chemistry. Medicine,

as pointed out by many of the great men of medicine, is an art. For a discussion

on the proper role of medicine I refer the reader to my paper titled

–Regimentation in Medicine and the Death of Creativity – on my website

(www.russellblaylockmd.com).

 

Most men of medicine recognize that some things are obvious without a placebo

controlled, double-blind, randomized study. For example, there has never been

such a study to see if smashing your finger with a hammer will be painful, but

we accept it without such pristine evidence. The same is true with removing

brain tumors or sewing up severe lacerations.

 

I find it interesting that there exist an incredible double standard when it

comes to our evidence versus theirs. The proponents of vaccination safety can

just say they are safe, without any supporting evidence what-so-ever, and it is

to be accepted without question. They can announce that mercury is not only

safe, but that it seems to actually increase the IQ, and we are to accept it.

They can proclaim thimerosal safe to use in vaccines without their having ever

been a single study on its safety in over 60 years of use, and we are to accept

it.

 

Yet, let me, or anyone else, suggest that excessive vaccination can increase the

risk of not only autism, but also schizophrenia and neurodegenerative diseases,

and they will scream like banshees –Where is the evidence? Where is the

evidence? When we produce study after study, they always proclaim them to be

insufficient evidence or unacceptable studies. More often than not, they just

completely ignore the evidence. This is despite the fact that we produce dozens

or even hundreds of studies that not only demonstrate the link clinically and

scientifically, but also clearly show the mechanism by which the damage is being

done –even on a molecular level. These include cell culture studies, mixed

cell cultures, organotypic tissue studies, in vivo animal studies using multiple

species and even human studies. To the defenders of vaccine safety-our evidence

is never sufficient and, if we face reality –never will be.

 

When I was in medical school, there was no proof that cigarette smoking cause

lung cancer. The connection was as obvious as the layman’s observation that

smashing your finger with a hammer would cause pain and even the town drunk knew

it was true, but to the medical elite –there was no proof.

 

No one had ever produced lung cancer in animals by exposing them to cigarette

smoke. In fact, my pathology professor, Dr. Jack Strong, had trained monkeys to

chain smoke, and after years of smoking none developed lung cancer. Yet, he was

convinced that smoking caused lung cancer. Dr. Alton Oschner, founder of the

famed Oschner Clinic in New Orleans, led the charge in proclaiming the link

between cigarette smoking and lung cancer. It took almost another decade before

the medical elite was willing to admit that smoking caused most cases of lung

cancer.

 

Almost 30 years passed from the time some iconoclastic men of medicine tried to

convince the medical establishment that smoking caused most cases of lung cancer

until it was generally accepted. The questions that needs to be asked is –How

many people died of lung cancer, the most prevalent cause of cancer death in the

United States, during this time? Data from the National Cancer Institute

estimated that in the year 2004, 157,000 people died of lung cancer. If 80% were

secondary to smoking that would be 125,000 dead. Over a ten-year period that

would be over one million dead and over 30 years almost 4 million people who

died from a preventable cause of death that at the time was still being hotly

debated by the medical purist. Lung cancer death rates were actually higher

during that time period.

 

So we see that questions of medical importance that are nick picked to death on

points of scientific purity can cost a lot of lives –millions of lives. There

are over one million children and even adults with autism and the numbers

continue to grow. This is a medial disaster of monumental proportions. The link

to the vaccine program is scientifically and logically compelling but these same

medical elitists refuse to listen.

 

Like smoking and lung cancer, we have enough proof today to call a halt to the

present excessive vaccine program and ban any level of mercury in vaccines. In

1983, before the autism epidemic began, children received 10 vaccinations before

attending school and the autism incidence was 1 in 10,000. Today they are

receiving 23 vaccines before age 2 years and 36 by the time they attend school

and the autism rate is now 1 in 150 births. Medical “experts†have provided

no other explanation for this dramatic and sudden rise in autism cases, despite

a draconian effort to find one.

 

They attempted to say it was genetic, but geneticists were quick to respond that

genetic disorders do not suddenly increase in such astronomical proportions.

They then said it was because of better diagnosis, despite the fact that the

diagnosis is obvious in virtually every case and that the criteria officially

accepted for diagnosis has become more restrictive not less.

 

When trapped by a lack of evidence, defenders of a nefarious position resort to

their old standby –the epidemiological study. Statisticians will tell you that

the least reliable type of study is an epidemiological study because it is easy

to manipulate the data so that the study tells you anything you wish it to.

Every defense offered by vaccine defenders is based on such studies and never

the actual science. Then they announce that the issue is settled and no further

studies need be done. After the media has been informed that the issue has been

settled, those who continue to present the evidence are considered kooks and the

great unwashed ignorant.

 

 

 

The Autism Disaster: Is it Man Made?

 

 

 

Today, specialists speak of the autism spectrum disorders (ASD), which include a

number of related neurodevelopmental disorders such as classical autism,

Rett’s syndrome, Asperger’s syndrome, childhood disintegrative disorder

(CDD) and pervasive developmental disorders not otherwise specified (PDD-NOS). I

have noticed over the years that when specialists know very little about a

disorder they spend an inordinate amount of time naming and sub-classifying it

–periodically. In addition they go to great lengths to define characteristics

and symptoms of the disorder that must be present to meet the criteria of

classification. Those who fail to meet these criteria are dispensed with into

another dimension, that is, they are ignored.

 

In the early 1980s, the incidence of autism was 1 in10,000 births. By 2005, the

incidence had leaped to 1 in 250 births and today it is 1 in 150 births and

still climbing.. One of the strongest links to this terrible set of disorders

was a drastic change in the vaccine programs of the United States and many other

countries, which included a dramatic increase in the number of vaccines being

given at a very early age. No other explanation has been forthcoming from the

medical elite.

 

In this paper I shall present evidence, some of which has not been adequately

discussed, that provides strong evidence for a connection between excessive

vaccination and neurodevelopmental disorders. In a paper I wrote in 2003, I

stated that removing the mercury from vaccines would help relieve the problem,

but it would not eliminate it. This was based on a number of studies in the

neuroscience literature that indicated that excessive and especially repeated

immune stimulation could result in severe disruption of brain development and

even neurodegeneration.

 

In this paper and a follow-up paper, I attributed the central mechanism to

excessive and prolonged microglial activation with an interaction between

inflammatory cytokines and glutamate receptor subtypes. The Vargas et al study,

published two years later in 2005, strongly supported this hypothesis, with the

finding of elevated inflammatory cytokines as well as the presence of extensive,

widespread activated microglia and astrocytes in examined autistic brains from

age 5 years to 44 years of age. This indicated that the brain’s immune

activation persisted for decades. Recent research indicates that this phenomenon

is not that uncommon and can be reproduced in the laboratory using a variety of

immune stimulating agents and neurotoxins, including mercury and aluminum.

 

 

 

Autoimmunity and Vaccinations

 

 

 

A number of studies have suggested a link between autoimmune disorders and

autism risk. Support comes from studies showing an increased risk of ASD in

children of mothers with autoimmune disorders.1-3 Yet, not all studies agree,

since at least one carefully done study found no strong link.4

 

Other more carefully done studies provided evidence suggesting some link.. For

example, in one study serum from a mother with an autistic child was found to

bind immunologically with specific brain cells (Purkinje cells).5 When this

serum was injected into pregnant mice, their babies demonstrated neurological

changes suggestive of autistic behavior, indicating a transfer of the

autoantibodies into the developing baby mouse.

 

A number of studies have found autoantibodies in a significantly higher number

of autistic children to various brain structures, such as serotonin receptors,

myelin basic protein, neuron axon filament protein, nerve growth factor and

cerebellar neurofilaments.6-10 It should be understood that these autoantibodies

are not found in all cases and that they may develop as a result of the damage

caused by the disease itself, rather than causing the disease. For example, we

know that after a stroke or head injury a substantial number of people will

develop autoantibodies to brain proteins. Never the less, the autoantibodies can

worsen the damage and prolong the damaging pathology.

 

It has also been demonstrated that methylmercury (from fish) and ethylmercury

(in thimerosal) are both powerful immunosuppressants and are associated with a

high incidence of autoimmunity.11 In this study, researchers found that unlike

methylmercury, thimerosal (ethylmercury) initially caused immune suppression and

then strong TH2-induced autoimmunity. They attributed this to the higher

conversion of ethylmercury to ionic mercury (Hg+) than seen with methylmercury.

In fact, one study found that strains of mice highly susceptible to developing

autoimmune diseases were sensitive to the ASD-like behavioral effects upon

mercury exposure, whereas mouse strains genetically not susceptible to

autoimmunity do not develop ASD behaviors.12 It is obvious from the extremely

high incidence of ASD that these autoimmune-related genes are very common, but

they remain silent until triggered by vaccines or other environmental toxins.

 

Immunologists have now concluded that autoimmune disorders are not the result of

excessive activation of a normal immune system, but rather activation of a

dysfunctional immune system. The question remains- what is causing such

widespread immune dysfunction among our population? Studies have shown that the

number of autoimmune diseases has increased over the past 30 years, with asthma,

type 1 diabetes and eczema rates increasing over two fold. There is also

compelling evidence to indicate that certain vaccinations are associated with

these autoimmune-related conditions.13,14

 

A compelling number of studies have shown an increase incidence of autoimmune

reactions in children with the autism spectrum disorders (ASD), especially

involving measles antigens, milk antigens and antibodies to gliadin and

gluten.15-17 Some of these have been shown to cross-react with brain-derived

proteins as well, especially those in the cerebellum, a major structure affected

in these disorders.18

 

Recently, neuroscientists have shown that much of the damage done in cases of

autoimmunity is not due to direct immune reactions with brain structures, but

rather results from the release of storms of free radicals and lipid

peroxidation products during the immune reaction, something I call a “hand

grenade in a shopping mall effectâ€. If you use a hand grenade to target a

single person in a crowd you will not only kill and injure the intended target,

but all of the bystanders as well.

 

Neuroscientists P.L. McGeer and E.G. McGeer have named this effect bystander

damage.19 The immune attack caused by the autoimmune reaction in the autistic

person’s brain damages a number of surrounding structures, especially brain

connections called dendrites and synapses. Subsequent studies have confirmed

that bystander damage is the most destructive reaction of autoimmunity.

 

Some studies, as referred to above, have shown that autism is much more common

in families with a hereditary tendency for autoimmune diseases, which makes

sense because they will have dysfunctional immune systems. There is also

compelling evidence that vaccines themselves can damage the immune system of

immature animals, leading to a higher incidence of autoimmunity and abnormal

brain development.20-24 Mercury, even in small concentrations, is also known to

induce autoimmunity in a high percentage of those exposed.11

 

Ironically, things that suppress a portion of the immune system, usually

cellular type immunity, increase the likelihood of autoimmunity. Immunologists

speak about a Th1 to Th2 shift and vice versa. This can occur with exposure to

mercury as well as in response to vaccination.25 A great number of autoimmune

diseases are associated with a Th2 shift.

 

The immune system is a very complex system, which at birth is incompletely

formed. This means, and has been confirmed in animal and human studies, that

immune reactions to vaccinations differ at different ages, so that small babies

have a different reaction than adults. This has been shown with the hepatitis B

vaccine now given to newborns. The rate of maturation of the immune system also

differs considerably among babies and children, meaning we cannot say what

effect will occur in all children. There are a great many variables, including

diet.

 

The immune system’s reaction to infection and immunization can be quite

different. Normally the immune system relies on a shifting of T-lymphocyte

function to determine which is better for the particular situation.26 The

T-helper lymphocytes (Th) can exist as either Th1, Th0, or Th2 forms. When no

infection is occurring, the system is in the Th0 mode (an uncommitted phase). If

a virus invades, it quickly switches to the Th1 phase, which allows immune cells

to secrete a group of cytokines that kill viruses. It also activates immune

lymphocytes that kill viruses and bacteria.. At other times, the immune system

needs a whole different set of immune signals and cells, which are supplied by

the Th2 phase. The Th2 phase favors the production of antibodies, mainly

supplied by B-cells, but in general they reduce immune reactions.

 

Infants are stuck in the Th2 mode during intrauterine life, so as to prevent

being immunologically rejected by the mother during pregnancy (much like

transplant rejection), since the baby is seen as a foreign body to the

mother’s immune system. Upon birth, the baby remains in a Th2 mode, but has a

limited ability to switch to the Th1 defensive mode if the need arises, say from

an infection. Months later the baby switches to the adult Th1 mode. If the

baby’s immune system remains in a Th2 mode, it has a high risk of developing

an autoimmune disorder, such as eczema, asthma or other allergies.

 

Presently, vaccine authorities recommend every baby be vaccinated with the

Hepatitis B vaccine at birth. But, is this safe? A recent study looked at the

immune reaction in newborn infants up to the age of one year who had received

the HepB vaccine to see if their immune reaction differed from adults getting

the same vaccine.27 What they found was that the infant, even after age one

year, did react differently. Their antibody levels were substantially higher

than adults (3-fold higher) and it remained higher throughout the study. In

essence, they found that the babies responded to the vaccine by having an

intense Th2 response that persisted long after it should have disappeared, a

completely abnormal response.

 

Autistic children have been described as having a Th2 predominance, which would

explain their propensity to developing autoimmune diseases and being more

susceptible to infections early in life.20,28-30 Elevated proinflammatory

cytokines, particularly TNF-, have been described in studies of the cytokine

profile in autistic children. As we shall see later, an excess production of

B-cell cytokines and suppression of T-lymphocyte TH1 activity, as seen in

autism, is associated with a high incidence of neurological damage by

excitotoxins.

 

Several things about these immune responses are important to all parents,

including effects of such immune overstimulation during pregnancy. For example,

it has been shown that excess immune stimulation, as occurs with vaccination,

can significantly increase the risk of a pregnant woman having a child with

autism or schizophrenia later in life, depending on when the vaccine is

given.31.32 In addition, persistent Th2 responses caused by the HepB vaccine

puts your child at a great risk of developing an autoimmune disorder and

impairing your baby’s ability to fight off infections. This means that

immediately after birth this vaccine has put your child at a greater risk of all

childhood related infections, including H. Influenza meningitis, meningiococcal

meningitis, rotavirus, measles, chickenpox, etc. Not only that, but numerous

studies have shown that such immune suppression greatly increases the number of

severe complications associated with these

infections, which means that should your child be exposed to measles or

chickenpox they are more likely to suffer neurological damage, seizures or other

systemic disorders.12,33,34 When this occurs, rather than admit that the science

indicates that the vaccine program is the cause of the complications and deaths,

the vaccine proponents scream that it demonstrates again the need for greater

efforts to vaccinate our children.

 

 

 

 

 

Immune Suppression By Live Virus Containing Vaccines

 

 

 

It is also known that certain viruses powerfully suppress immunity, such as the

measles virus.35 The MMR vaccine contains live measles viruses and recent

studies have shown that immune suppression after vaccination with this virus

suppresses immunity in a profound way that last as long as six months.36-41 In

fact, the CDC recommends separating this vaccine from other live virus vaccines

to prevent viral overgrowth (Yet, they combine it with two other live

viruses-rubella and mumps viruses).

 

Yet, they never address the obvious question –wouldn’t this vaccine also

make the child more susceptible to other naturally occurring infections such as

hemophilus B influenza meningitis, meningococcal meningitis, persistent measles

infection, influenza infection and even chickenpox? This has been strongly

suggested by a number of studies.42 Not only would they be more susceptible, but

severe complications and even death would be more common as well.

 

When death and severe complications occur due to these infections,

pediatricians, the CDC and the American Academy of Pediatrics use this as a

justification for more vaccines, never admitting that the increase incidence of

these infections and complications was caused by their previous vaccine

recommendations.

 

This risk is especially high in families with a number of other children in the

household or in children in day care centers. With a prolonged suppressed immune

system, exposure to other sick children would put this child at a high risk of

contracting the infection and of having complications or dying from the

infection as stated.

 

Studies have also shown that vaccines that cover only a few strains of a virus

or bacteria that naturally have a great number of strains (some have over a

hundred strains), can cause a shift in strain dominance so that the strain not

included in the vaccine then becomes the dominant disease causing strain. We see

this with the meningiococcal and pneumococcal vaccines.43-45 This is discussed

in the scientific literature but the public is never informed. Most

pediatricians are completely unaware of this.

 

When combined with mercury, which is also an immune suppressing substance, the

effect is compounded. Fluoroaluminum, formed in fluoridated drinking water, also

interferes with immune function, as do many insecticides and herbicides used

around the home.46

 

Often forgotten, is the substantial evidence that omega-6 oils powerfully induce

inflammation and immune suppression when consumed in large amounts. Those eating

a Western diet are consuming 50-fold higher amounts of this type of oil (called

linoleic acid) than needed for health. These oils include corn, safflower,

sunflower, canola, peanut and soybean oils. So, we see that the average child is

exposed to a number of substances in their food and environment that can also

alter immunity, making them not only more susceptible to natural infection, but

also to vaccine complications.

 

In essence, by overvaccinating our children, public health officials are

weakening their immune system, making them more susceptible to a number of

infections and less able to combat the infections. This gives them an endless

source of “horror stories†to justify even more vaccines. Remember also that

mercury is an immune suppressant, that both from vaccines and seafood

contamination.

 

One can see that a pregnant mother having dental amalgam fillings who eats a

diet high in methylmercury-containing seafood and living in an area with high

atmospheric mercury, such as West Texas, would be at a greater risk of having an

autistic child than one not exposed to these other sources of mercury. These

differences in environmental mercury exposure are never considered by those

insisting all children have the same vaccines, including mercury-containing

vaccines such as the flu vaccine.

 

 

 

The Autistic Prone Child

 

 

 

What is becoming obvious is that certain children are at a higher risk of

developing autism than others, for a variety of reasons. It is also obvious that

these newborns and small children develop infections at a higher rate than less

vulnerable children. This may be because of a developmental immune deficiency,

which can affect only a portion of the immune system and so be easily missed by

their pediatrician. Indeed, it has been noted that a great number of cases of

childhood immune deficiencies are missed by practicing pediatricians, especially

the more subtle cases, which may make up the majority of ASD-prone children.

 

For example, many physicians treating autistic children have noted a high

incidence of ear infections. These are treated with broad-spectrum antibiotics,

which often lead to a high incidence of Candida overgrowth in the child’s

body. Both infections will prime the microglia in the child’s brain –which

is the brain’s specific resident immune cell. This priming effect shifts these

normally resting microglia immune cells into overdrive.47 If stimulated again

within weeks or even months, they generate extremely high levels of free

radicals, lipid peroxidation products, inflammatory cytokines and two

excitotoxins glutamate and quinolinic acid.48 Studies have shown that this is

the major mechanism for both viral and vaccine-related brain injury.

 

The high incidence of infection in these children indicates the possibility of

preexisting immune system dysfunction. As stated, this also increases the risk

of an autoimmune reaction. The stage is then set for the autism cascade to

develop and this can be triggered by early vaccination or a recurrent infection.

Remember, the microglia have been primed, either by a natural infection or an

earlier vaccination (such as the hepatitis B vaccine given soon after birth).

The vaccine is different from a natural infection in that the vaccine produces

brain immune stimulation for very prolonged periods.

 

It has been proven, in both animal studies and human studies, that systemic

infections or immune activation by vaccines, rapidly activate the brain’s

microglial system and can do so for prolonged periods.49-53 Once the primed

microglia are reactivated by the subsequent vaccination or infection, the

microglia activate fully and pour out their destructive elements as discussed

above.

 

With a natural infection, the immune system quickly clears the infection and

then shuts off the immune activation, thus allowing repair of what damage was

done. This shutting down of the microglia is very important. There is evidence

that with repeated and excessive vaccine-triggered immune stimulation, the

microglia do not shut down.47 This is what was found in the Vargas et al study,

in which they examined the brains of 11 autistics from age 5 years to 44 years

of age dying without active infectious diseases as compared to age matched

controls.54 That is, they found widespread activation of inflammatory cells

(microglia and astrocytes) in the brains of the autistic patients. This explains

the widespread brain damage seen in all autism cases.

 

This study was one of the most carefully conducted, extensive examinations of

the immune reactions in the autistic brain ever done and involved

immunocytochemistry, cytokine protein assays and enzyme-linked immunoascorbant

assays of the brain tissue. They also performed similar assays of spinal fluid

from an additional six living autistic patients, which confirmed the intense

immune activation and inflammation.

 

The average child receiving all of the recommended vaccines will have some 23

inoculations by age two years and 36 by the time they enter school. Most of

these will be spaced within one month of each other, which means the priming and

activation cycle of the microglia will be continuous. In addition, should they

follow the new CDC recommendation, they will receive the flu vaccine every year

starting at age 6 month through age 18 years. These vaccines contain a full dose

of thimerosal mercury.

 

In addition, we must consider the effect of the measles and rubella portions of

the MMR vaccine, which begins at age 1 year. The profound immune suppression,

which last up to 6 months after it is given, will not only increase the risk of

developing other infections, but will increase the risk of an autoimmune

reaction. Cytomegalovirus is also a powerful immune suppressing virus that

commonly infects newborns and small children, especially if they are immune

suppressed. So, we see that giving a live, immunosuppressant vaccine early in

life can dramatically increase the risk of autoimmune disorders, increase

microglial brain injury as well as increase the risk of infection by other

immune-suppressing viruses and pathogenic organisms. And, it dramatically

increases the risk of your child developing one of the autism spectrum

disorders.

 

It should also be appreciated that the Candida infections in these children

trigger a prolonged systemic immune reaction, which means a prolonged brain

immune response as well and a worsening of any autoimmune disorder it may have

produced..

 

 

 

Seizures and Autism

 

 

 

It is estimated that 30% to as high as 82% of autistic children develop

seizures, depending on the sensitivity of the examination.55-56 Growing evidence

indicates that there is a close correlation between brain inflammation (by

microglial released inflammatory cytokines and glutamate) and seizures, just as

we see with excessive brain immune stimulation with vaccines. Using

lipopolysacchride as a vaccine-based immune stimulant, scientists have induced

seizures in experimental animals of various species.57,58

 

A considerable amount of evidence links excitotoxicity and seizures. In

addition, a number of the newer antiseizure medications work by blocking

glutamate receptors or preventing glutamate release. One of the central

mechanisms linking excessive immune stimulation with seizures, as with vaccines,

is the induced release of the excitotoxin glutamate and quinolinic acid from

immune stimulated microglia and astrocytes.59-61

 

In many cases these seizures are clinically silent or manifest as behavioral

problems, often not recognized by pediatricians as seizures. Yet, they can alter

brain function and eventually result in abnormal brain development. Even the CDC

and American Academy of Pediatrics recognizes that infants and children with a

history of seizure should not be vaccinated.

 

It is also known that autistic children who regress, that is begin to show a

sudden worsening of mental development, have a significantly higher incidence of

seizures, both clinical and subclinical, than those who do not regress.

Interestingly, studies have shown that during early brain development after

birth the number of glutamate receptors (that trigger the seizures) increase

steadily until the age of 2 when it peaks.62 Thereafter they decline in number.

This means that the immature brain is significantly more susceptible to seizures

than the more mature brain and this is when your child is being given 23 vaccine

inoculations, many of which are associated with a high incidence of seizure.

 

Let just use the case of the 1 year-old child who is taken by his mother for his

vaccines and the pediatrician convinces the mother to allow him/her to give all

five vaccines recommended for that age group at that one office visit. After

all, both the CDC and the American Academy of Pediatrics assures mothers and

fathers that it is completely safe to give them all at once. This not only means

that the child’s immune system will be assaulted by 7 different antigens

(viruses, three of which are alive) but by five full doses of immune adjuvant

–a powerful mix of immune stimulating chemicals.

 

This intense immune stimulation not only results in a red, swollen and painful

site where the shots were given, but a hyperintense activation of the brain’s

immune system. Mothers and fathers are familiar with the high-pitched crying

their babies have after such a series of vaccines. Often, this high pitched

crying, lethargy and poor feeding last weeks to months. This is not due to the

pain of the injection, as the pediatrician will assure you, rather it is

secondary to brain inflammation –what we call an encephalitic cry.63

 

Recently, information was released that the combination vaccine by Merck,

ProQuid resulted in twice as many seizures as giving the vaccines separately.

This vaccine contains the MMR antigens as well as chickenpox viral antigen (in a

dose 5x that of the single vaccine). The study was conducted by comparing 43,000

kids getting the ProQuid vaccine versus those getting the shots separately.

While they attributed the increased seizures to fever caused by the vaccine,

this is only part of the story.

 

I have seen a number of febrile seizures during my neurosurgical practice and my

research indicates that the reason some kids are susceptible to febrile seizures

and not others is that the susceptible ones are deficient in neuroprotective

nutrients and are often exposed to neurotoxic substances, such as mercury and

aluminum, that increase sensitivity to seizures. Consistently found in the

studies of febrile seizures is the presence of low blood sodium levels (called

hyponatremia).64

 

It is known in neurology that very low sodium blood levels can trigger seizures,

even in normal people. It can also result in rapid coma and death, especially in

a child. In the presence of brain inflammation, the incidence of hyponatremic

seizures is much higher. One of the major causes of hyponatremia in infants and

small children is the doctor giving IV fluids that contain little or no sodium

chloride (salt). During my practice I constantly tried to convince pediatricians

to stop using D5W (5% dextrose and water) as an IV solution in sick children,

because it induced seizures. I am convinced that a significant number of

children who died following a meningitis infection actually died of hyponatremia

induced by a combination of the infection and the pediatrician giving hypotonic

IV fluids (D5W) during treatment.

 

I will always remember the case of a little girl who developed H. Influenza

meningitis and was in a deep coma. The pediatricians consulted me, suspecting a

brain abscess.. This was quickly ruled out. I noted the child was getting D5W as

an IV solution. A simple blood test demonstrated she had severe hyponatremia.

Because she was comatose, the pediatricians wanted me to let her die. I refused.

They even went so far as to approach my partners to have them take me off the

case. Fortunately, they refused to intervene. I corrected her sodium deficiency

and she made a good recovery and had no further seizures.

 

Studies have also shown that glutamate, as MSG, given to small animals with

immature nervous systems, also increase the likelihood of seizures from other

causes, such as fever.65,66 Excess vaccination, increases brain levels of

glutamate.

 

Keep in mind that the child by age one will already have had 20 vaccine

inoculations, each spaced no more than one or two months apart. This means the

brain microglia are maintained in a constant primed state. Each vaccine

increases dramatically the damage done by the previous vaccine series. One is

not surprised that so many vaccinated children develop seizures, often

repetitive seizures, or that we have such a high incidence of autism. And I can

assure the elite of the American Academy of Pediatrics and the CDC that over one

million autistic children far exceeds the danger measles, mumps, diphtheria,

chickenpox, tetanus, rotavirus, HiB meningitis and hepatitis pose to our youth.

Also, keep in mind that for every fully autistic child there are ten times that

many with lesser degrees of impairment.

 

Compelling evidence indicates that the death rates from the childhood vaccines

fell dramatically in developed countries prior to the mass vaccination programs,

as documented in Neil Z. Miller’s book, Vaccines: Are They Really Safe and

Effective?.67 Objective studies attribute the fall in death rates to better

nutrition and improved public sanitation. So, when you hear health authorities

warn that stopping the present vaccine program will mean a return of millions of

children dead from childhood diseases, they are lying and know they are lying.

 

 

 

Human Brain Development is Different

 

 

 

The human being has an unusual brain development in that there is a prolonged

period of maturation and neuroanatomical pathway development occurring years

after birth. The most rapid brain development occurs during the last trimester

of intrauterine life and two years after birth –what is referred to as the

brain growth spurt. It is the areas regulating higher brain functions, such as

emotions, emotional control, thinking, complex memory and language function that

is last to develop.

 

Recent studies using functional MRI scans (fMRI) and PET scanning have shown

that brain development continues until about age 26 or 27. Using such brain

mapping techniques as volumetric parcellations that give a 3-D view of the

brain, researchers examined the brains of 13 children followed for 10 years with

scans being done every 2 years.68 What they found is that there was an

overdevelopment of synaptic connections after birth that was slowly removed

(called pruning) in developmental cycles during early childhood and even

adolescence. For example, around age 4 to 8 years there was a thinning of the

cortex in the language areas of the brain (parietal lobes) that spread to the

temporal lobes and finally to the frontal lobes. This thinning moved the brain

into a more functional state of development, that is, it got rid of unnecessary

pathways and connections-sort of a final correction.

 

Further, they found that the language areas of the brain matured around age 11

to 13 years and the brain areas controlling higher brain function, the

prefrontal cortex, matured in the mid twenties.69,70 What this means is that

during the first two years of life, the child’s brain is undergoing rapid and

very critical development and that the more advanced cognitive portions of the

brain continued their development even later –much later.

 

There is compelling evidence that the pruning of these excess synapses is

essential. Otherwise the brain would be inundated with an enormous array of

competing signals –that is a lot of static and misinterpreted messages. This

pruning process, as well as the growth, maturation and migration of neurons, is

carried out by a combination of signals, which include carefully controlled

fluctuating glutamate brain levels and appearance of specific microglia-released

cytokines in a timed sequence.63,71-75 This is all very exacting and easily

disturbed by a number of toxins, such as mercury and aluminum. It is also

critically dependent on the presence of thyroid hormone.

 

Anything that alters these fluctuating glutamate and cytokine levels can affect,

sometimes in drastic ways, the development of the brain, which as we have seen

continues far into young adulthood.76-79

 

Pathological studies of autistic brains demonstrate three areas that are

especially affected –the cerebellum, the limbic brain and the prefrontal

area.80-83 There exist intimate connections between the cerebellum and the

prefrontal cortex and between the prefrontal cortex and the limbic system –in

particular the amygdalar nuclei. These are also areas frequently affected by

inflammatory cytokines during immune stimulation, such as with vaccinations.84

In the Vargas et al study, the most intense microglial activation was in the

cerebellum.54

 

In low concentrations, both the cytokines and glutamate act to protect

developing brain cells and promote brain development (neurotrophic function),

but in higher concentrations they can be very destructive, especially in

combination. Of particular importance are the inflammatory cytokines interleukin

1 and 1ß (IL-1 and IL-ß), IL-6 and tumor necrosis factor-alpha (TNF-).85-89

 

Evidence that alteration in these cytokines can cause developmental brain

problems comes from in part from studies of schizophrenia, a disorder that can

be produced by stimulating inflammatory cytokine surges during pregnancy.90-92

It is known, for example, that women who are infected with the flu during

pregnancy are significantly more likely to give birth to an autistic child or a

child with schizophrenia, depending on when the infection occurs. At first, they

assumed this was due to the virus being passed to the fetus, but subsequent

studies found that it was not the virus, but the mother’s immune reaction that

cause the problem –that is, it was the immune cytokines (IL-1, IL-2, Il-8,

IL-6 and TNF-) that was causing the injury to the baby’s developing brain.

 

The insane policy of having every pregnant woman vaccinated with the flu vaccine

flies in the face of what we know concerning the neurotoxic effect of excessive

immune stimulation during pregnancy. Even if the vaccine prevented the flu

(studies show it reduces it only in a select few), instead of a small percentage

of pregnant women being at risk, they would make sure every woman was at risk.

Keep in mind these pregnant women will have been receiving the flu shot

(containing mercury) every year since age 6 months (according to present CDC

recommendations) meaning they will have accumulated a significant amount of

mercury and will, as a result, have a hyperintense cytokine response to the flu

vaccine during their pregnancy. In addition, they will have accumulated a

significant amount of neurotoxic mercury.

 

It is also important to keep in mind that the immune activation with vaccination

differs from natural immunity, in that it persist much longer –even for years

following a vaccination. This does not allow the brain time to repair itself

either in the mother or in the unborn child. In addition, the way the immune

system reacts differs with vaccination, especially in the very young, as we have

seen.

 

A new study from the Weizmann Institute in Israel by Hadas Schori and co-workers

found that with a normally functioning immune system, the T-lymphocytes actually

protected neurons from glutamate excitotoxicity, but if the immune system was

dysfunctional, as seen in most of the ASD children, the opposite happened.93

That is, stimulating the immune system was significantly destructive of the

brain’s cells. Their study found that under conditions of immune dysfunction,

B-cells predominated in invading the brain and this dramatically increased the

destructive effect of excess glutamate.

 

Another study also found that mercury toxicity was greatest in mice prone to

develop autoimmune diseases, thus confirming the above study.12 Further, the

Schori study indicates that even in animals without an autoimmune-prone genetic

makeup, suppression of T-lymphocyte function increased excitotoxic damage. Both

the measles and cytomegalovirus inhibit T-cell function, as does mercury and the

hepatitis B vaccine.11,27,35,41,

 

The Vargas et al study also demonstrated that T-lymphocytes failed to infiltrate

the autistic brains examined, meaning that the protective T-lymphocyte

protection was not in evidence.54 Under these conditions, systemic immune

activation, as seen with multiple and sequential vaccinations, would increase

the excitotoxic damage caused by the microglial and astrocytic activation.

 

When all the evidence is taken together, these studies provide powerful evidence

that sequential, multiple vaccinations in newborns and small children maximizes

the inflammation of the brain and as a consequence dramatically enhances the

excitotoxic pathology, and does so for prolonged periods (decades). The more

vaccines that are added to the vaccine schedule, the more frequently this

devastating effect will be seen and in worse forms.

 

 

 

What About the Adjuvants Used in Vaccines?

 

 

 

While mercury has gotten all the attention, aluminum (found in most vaccines) is

also a major culprit in this shocking saga. Added to most vaccine are a number

of substances either used during manufacturing or designed as an immune booster

(adjuvant). These include albumin, aluminum (either as aluminum hydroxide,

aluminum phosphate or alum also known as aluminum potassium sulfate), various

amino acids, DNA residues, egg protein, gelatin, monosodium glutamate (MSG),

MRC-5 cellular protein and various antibiotics. Not listed on official lists are

bacterial and viral contaminants, which can include their particulate,

fragmented matter.94-99

 

The purpose of the aluminum compounds is to dramatically boost the immune

reaction to the vaccine and make it prolonged, since some of the aluminum

remains in the site of injection for years. Aluminum was first added to vaccines

in 1926. Many of the other components added to the vaccines also boost immunity,

especially that of undesirable components of the immune system, such as the

B-cells.

 

Because these vaccine adjuvants are designed to produce a prolonged immune

stimulation, they pose a particular hazard to the developing nervous system..

Studies have shown that immune activation can last as long as two years after

vaccination. This means that the brain’s microglial cells are also primed for

the same length of time, and possibly longer.

 

A new emerging syndrome called macrophagic myofasciitis has been attributed to

the aluminum adjuvant in vaccines and is especially associated with the

hepatitis B vaccine and the tetanus vaccine.100 Victims of this syndrome suffer

severe muscle and joint pains and severe weakness. Subsequent studies, since the

syndrome was first described in France, indicate widespread, severe brain injury

as well, as confirmed by MRI scanning.101,102 This brain syndrome has been

described in American children as well.

 

It is known that aluminum accumulates in the brain and results in

neurodegeneration. The evidence for a link between aluminum neurotoxicity and

Alzheimer’s disease continues to grow stronger. Aluminum, like mercury,

activates microglia leading to chronic brain inflammation, which is a major

event in both Alzheimer’s disease and Parkinson’s disease.103-110

 

Flarend and co-workers studied the fate of vaccine injected aluminum in the dose

approved by the FDA (0.85 mg per dose) using radiolabeled aluminum adjuvant

–either aluminum hydroxide or aluminum phosphate, the two approved forms of

adjuvants used in vaccines.111 They found that the aluminum was rapidly absorbed

into the blood from both forms of aluminum, but that the aluminum phosphate was

absorbed faster and produced tissue levels 2.9x higher than aluminum hydroxide.

Blood levels of aluminum remained elevated for 28 days with both adjuvants.

Elevated aluminum levels were found in the kidney, spleen, liver, heart, lymph

nodes and brain.

 

This indicates that aluminum from vaccines is redistributed to numerous organs

including brain, where it accumulates. Each vaccine adds to this tissue level of

aluminum. If we calculate the total aluminum dose from 36 vaccines, we see that

the total dose is 30.6 mg and not the 0.85 mg considered safe by the FDA. Of

course not all this aluminum ends up in the tissues, but they will accumulate

substantial amounts, especially when added to the amount from foods and drinking

water. When a number of aluminum-containing vaccines are given during a single

office visit, aluminum blood levels rise rapidly and to much higher levels and

this elevation persist for over a month, all the time infiltrating the tissues,

including the brain with aluminum.

 

It is also known that aluminum enhances the toxicity of mercury and that

aluminum, even from other sources, increases inflammation in the body.106 The

question no one seems to be asking is -does the aluminum act as a constant

source of brain inflammation? Research, especially that showing

aluminum-triggered microglial activation, seems to indicate it does.112 Dr.

Anna, Strunecka, a professor of physiology, found that aluminum readily binds

with fluoride to form fluoroaluminum and that this compound can active G-protein

receptors, which controls a number of neurotransmitters, including glutamate

receptors.46 Giving multiple aluminum-containing vaccines at once would raise

blood and tissue levels much higher than when give separately, thus increasing

brain levels as well. Fluoride in drinking water, foods and dental treatments

would react with the brain aluminum, creating the neurotoxic fluoroaluminum

combination. Studies have shown that fluoride also

accumulates in the brain.

 

 

 

The Role of Mercury in Developmental Brain Damage

 

 

 

Mercury also activates microglia and does so in concentrations below 0.5

microgram (3 to 5 nanograms).113 This is well below the concentration seen with

giving mercury-containing vaccines to children. Ethylmercury, like its cousin

methylmercury, enters the brain very easily but once within the brain it is

de-ethylated, forming ionic mercury (Hg+).114 There is evidence that ionic

mercury is significantly more neurotoxic than organic mercury. Once it is

converted, the mercury is difficult, if not impossible, to remove. Studies using

monkeys demonstrated that ionic mercury is redistributed in the brain.115 These

same series of studies also demonstrated that there was extensive microglial

activation in the monkey’s brain and it persisted over 6 months after the

mercury dosing was stopped, indicating that even when the plasma mercury

disappears the brain mercury remains.116

 

This is important to remember when you hear from the vaccine safety promoters

that new studies have shown that ethylmercury (in thimerosal) disappears from

the blood within several days. Actually, the mercury leaves the plasma and

enters the brain, where it is de-ethylated and remains for a lifetime. What they

fail to mention is that recent studies have shown that only 7% of methylmercury

is converted to ionic mercury, whereas 34% of ethylmercury is converted within a

short time.117 This means that more of the most destructive form of mercury is

retained in the brain following mercury-containing vaccine exposure than

exposure to mercury from fish.

 

They also fail to mention that the vaccine-based mercury that was removed from

the blood enters the stool in high concentrations, where it recirculates

repetitively, meaning that with each cycle the mercury has access to the brain.

 

Mercury has another link to this immune/excitotoxic reaction. A number of

studies have shown that mercury, in submicromolar concentrations, interferes

with the removal of glutamate from the extracellular space, where it causes

excitotoxicity.118-120 This removal system is very important, not only in

protecting the brain but also in preventing abnormal alterations in brain

formation.121 As you will recall, it is the carefully programmed rise and fall

in glutamate levels in the brain that allow the brain’s pathways to develop

and for proper development of its connections (called synaptogenesis).

 

Another way mercury damages the brain is by interfering with its energy

production. The mitochondria of the neuron (the energy factory) accumulate more

mercury than any other part of the cell. It is known that when you interfere

with the neuron’s ability to produce energy, you greatly magnify its

sensitivity to excitotoxicity, so much so that even physiological concentrations

of glutamate can become excitotoxic.124,125

 

One of the destructive reactions of both excitotoxicity and mercury toxicity is

the generation of storms of free radicals and lipid peroxidation products.

Essential to the protection of brain cells is the antioxidant enzymes (catalase,

glutathione peroxidase and SOD). Mercury poisons these protective enzymes.

 

One of the most important protective systems is the glutathione molecule, which

is present in every cell in the body. Mercury dramatically lowers glutathione

levels by a number of mechanisms. (See Dr. Boyd Haley’s work for more

information).126 So, we see that mercury can greatly aggravate this entire

destructive mechanism.

 

It is important to appreciate that as important as mercury is, it is not the

lone essential element in this process. Rather, essential to this process is a

combination of pre-existing or vaccine-induced immune dysfunction and excess

immune stimulation by a crowded vaccine schedule. This is why autism will not go

away, even when mercury is completely removed from all vaccines. It also

important to appreciate that mercury can never be removed from the picture

because of the numerous sources of mercury in our environment, such as

contaminated seafood, atmospheric mercury and dental amalgam.

 

 

 

Why Males Are Affected More Often

 

 

 

One of the enigmas of autism is why it occurs in males more often than females.

Actually there are a number of toxins that have this gender selectivity. Studies

have shown, for example, that both mercury and monosodium glutamate (MSG) have

greater neurotoxicity in males than females.127 The reason appears to be the

enhancing effect of testosterone on both substances’ toxicity.128,129

 

Glutamate is the most abundant neurotransmitter in the brain and operates

through a very complex series of receptors (3 major inotropic receptors- NMDA,

AMPA and kainite receptors, and 8 metabotropic receptors). As stated, the

presence of glutamate outside brain neurons, even in very small concentrations,

is brain cell toxic. Because of this, the brain is equipped with a very

elaborate series of mechanisms to remove glutamate quickly, primarily by

utilizing glutamate uptake proteins (EAAT1-5). Mercury, aluminum, free radicals,

lipid peroxidation products and inflammatory cytokines can easily damage these.

130,131

 

One of the important ways glutamate regulates neuron function is by allowing

calcium to enter the cell and by the release of calcium within cell storage

depots. When calcium (glutamate operated) channels are opened, the calcium flows

in as a wave of concentrated calcium. These are referred to a calcium waves or

oscillations. They regulate a number of neuron functions, one of which plays a

vital role in brain development.

 

During brain development, the future neurons are lined up along membranes within

the core of the undeveloped brain. These cells must migrate outwardly to reach

their final destination and they do so by guided chemical signals mainly

released by microglia and astrocytes. These trillions of connections also

develop during a process called synaptogeneis, and use many of the same signals.

 

Studies have shown that the calcium waves cause developing brain cells to

migrate, which is essential for development of the brain (it forms the

architectonic structures and functional columns of the brain).132 Interestingly,

testosterone also affects embryonic brain cell migration by regulating calcium

waves, and mercury, probably by stimulating glutamate release, does the same

thing.133 Estrogen reduces calcium oscillations and stops the migration. Other

chemical signals in the brain also play a role (reelin).

 

If calcium oscillations are not properly regulated, that is- there are too many

calcium oscillations, the brain develops abnormally. Testosterone and glutamate

have an additive effect on these calcium waves. In this way, testosterone

enhances the damaging effect of excessive glutamate and mercury.

 

Studies have shown that higher doses of MSG during brain formation can cause

abnormalities of brain development that closely resemble mercury poisoning and

the toxic effects of high levels of inflammatory cytokines.76 Interestingly,

vaccination has been shown to significantly increase the toxicity of several

other neurotoxins, so much so that they can trigger brain cell destruction or

synaptic loss even when subtoxic concentrations of the toxicants are used.

Testosterone aggravates this toxicity as well.

 

Studies of autistic children show an elevated level of androgens in most, even

in female autistic children.134 In general, androgens, such as testosterone,

enhance neurological injury and estrogens tend to be protective of the brain.135

 

 

 

The Role of the Leaky Gut Phenomenon and Food Intolerances.

 

 

 

Wakefield and his co-workers demonstrated a connection between the MMR vaccines

and abnormal gut function in a landmark article appearing in the journal Lancet

in 1998.136 In this carefully conducted study they biopsied the lining of the

intestines of autistic children having GI symptoms and demonstrated lymphocytic

infiltration as well as elevated levels of inflammatory antibodies and

cytokines. TNF- release was particularly high from these gut-based immune cells.

The entire GI tract, from the stomach to the colon, was infiltrated by these

immune cells.

 

Subsequent studies have shown a high incidence of abdominal pain, bloating,

diarrhea and constipation in children with ASD.138,139 A number of other studies

have shown problems with digestive enzymes, defective detoxification, and an

overgrowth of a number of pathogenic bacteria and fungi in the colon and

intestine of ASD children.140,141

 

Not surprisingly, a few studies have shown significant improvement in behavior

when ASD children are placed on diets devoid of identified food

allergens.142-144 Antibodies to food components, such as casein, gliadin and

gluten have also been described as well as cross-reactions between food antigens

and brain components.145

 

One disease that closely resembles the case of ASD in terms of brain injury

associated with food allergins is celiac disease, in which there is an immune

sensitivity to the food components gliadin and gluten. Approximately 6% of such

patients will demonstrate neurological damage, most frequently cerebellar

ataxia.146 Other studies have also found seizures, cranial nerve damage,

dementia and impaired frontal lobe function.147-151

 

Autopsy studies indicate that the most commonly found neurological damage occurs

in the cerebellum, as we see in autism. Other studies have shown an immunologic

cross-reactivity between gluten antibiodies and Purkinje cells in the

cerebellum.144 Like the celiac cases, in autism the most intense microglia

activation and neuronal loss occurred in the cerebellum. In many of the cases of

autistic brains examined, virtually all of the Purkinje cells were lost.54

 

Studies looking for the incidence of GI symptoms in autistic children indicate

that from 20% to 84% will have complaints. It is interesting to note that in the

studies on celiac-related neurological problems, only 13% complained of GI

symptoms, so ASD children can have gut-related brain effects without obvious GI

symptoms.154

 

Some feel that the gliadin, casein and gluten can be converted to opioid-like

substances, such as gliadomorphin and casomorphin that can produce a morphine

response in the brain, leading to abnormal behavior.152 These opioids also

suppress immunity and increase excitotoxicity.154 While the opioid effect

exists, I feel it is the recurrent immune stimulation of primed microglia that

is causing most of the damage seen in autism.155

 

Studies have also found frequent dysbiosis in autistic children, that is, an

overgrowth of pathogenic bacteria and fungi and a loss of beneficial probiotics

organisms.138 It has been demonstrated that Candida organisms can penetrate the

gut wall and enter the blood stream, were they can be distributed to all tissues

and organs, including the brain.156 The same is true for pathogenic bacteria and

bacterial toxins. These brain implanted organisms act as continuous sources of

immune stimulation, which is especially damaging to the brain because of

vaccine-triggered microglia priming and/or activation occurring before the gut

problem presents itself, with repeated vaccination aggravating the injury.

 

With each subsequent vaccination, the microglia response is enhanced because of

the recurrent immune activation by food antigens and microbiological antigens.

It is interesting to note that trials of antibiotic vancomycin, which is not

absorbed from the gut, objectively improved the cognitive function of a number

of autistic children.157 We also know that with children having celiac disease

even a very small amount of the offending food can have devastating neurological

effects.

 

 

 

Conclusion

 

 

 

I have presented a considerable amount of evidence for a connection between the

present vaccine schedule and the development of autism spectrum disorders, yet

even this paper is only a brief review of what we know. A more in-depth

discussion of the immune/excitotoxic will appear in my paper- Interaction of

activated microglia, excitotoxicity, reactive oxygen and nitrogen species, lipid

peroxidation products and elevated androgens in autism spectrum disorders, which

will appear in an upcoming special autism issue of the journal-Alternative

Therapies in Health and Medicine.

 

Much of this information is being totally ignored by the medical elite and

especially the media. The Simsonwood conference proceedings, in which over 50

scientists, vaccine pharmaceutical company representatives and representatives

from the World Health Organization met secretly in Norcross, Georgia, disclosed

that the safety of your children is not their primary interest –their only

interest is selling vaccines to the public. A friend of mine, while speaking to

an audience of scientists and public health officials in Italy, was rudely told

by a public health official that (paraphrased) –We all know that vaccines can

cause neurological damage, but we must keep this from the public because it

might endanger the vaccine program.

 

It is also important to understand that most practicing pediatricians have never

heard what I have disclosed to you. Most have very little understanding of

immune function and have no idea of the pathological effect on the brain of

giving multiple vaccines on a large scale. These effects are widely discussed in

the neuroscience literature, but few practicing physicians, especially

pediatricians, ever read such articles.

 

Immunology, like nutrition, gets only scant attention in medical school and even

less in residency training of physicians. Older doctors have no concept of the

newer discoveries in immunology, especially neuroimmunology. The human immune

system is one of the most complex systems in physiology and our studies indicate

an even greater complexity is to be found. Despite a renewed interest in the

immune system’s function in neonates and small children, much remains unknown

concerning the immune effects of exposing infants and small children to such a

large barrage of vaccine early in life. Yet, what we do know is that they react

quite differently than adults and it can have devastating consequences on brain

development and function.

 

Vaccinating millions of children with the hepatitis B vaccine at birth can only

be described as dangerous idiocy. The vast majority of infants, children and

adolescents are in no danger from this infection- even the medical authorities

agree on that. It is also known that the effectiveness of the vaccine in

children last no more than two years and has little or no effectiveness in the

immune suppressed child. The nefarious plan by these vaccine geniuses is to

force vaccines all babies, since they would have difficulty convincing adults,

that is, the one at any danger, to get the vaccine.

 

The problem with this “plan†is that the vaccine is ineffective by the time

the child reaches the age of risk. Now that they have discovered this, they are

recommending that all children have a booster vaccine every two years.

 

The American Academy of Pediatrics and the CDC, the forces behind this vaccine

mania, assure parents that giving all of the required vaccines at once is

perfectly safe. As we have seen, the scientific “evidence†does not support

this policy. To do so exposes the child to a high concentration of

immune-stimulating adjuvants that will intensely activate the brain’s immune

system (microglia) during the brain’s most active growth period, that is,

during the first 2 to 6 years of life. The maturation and development of the

brain continues to a large degree throughout adolescence. As we have seen,

excessive vaccination can result in brain inflammation and brain swelling that

can be prolonged, even lasting years, if not decades (as we have seen in the

Vargas et al study). This can result in seizures, high pitched crying, severe

lethargy, weakness and behavioral problems, such as agitation, depression, anger

and other autistic behaviors.

 

In addition, giving the vaccines all at once exposes the brain to higher levels

of neurotoxic aluminum as proven by radiolabeled aluminum study quoted above. If

a person were to follow recommended vaccine guidelines they would receive over

100 vaccines in a lifetime. Because of the way the vaccines are given, this

would not allow the brain’s microglial cells to shut down, which is essential.

 

One of the effects of chronic microglial activation, other than brain

inflammation, is an elevation in brain glutamate levels. Studies have shown this

can lead to chronic neurodegeneration and is suspected as a common mechanism

associated with neuropathic viruses, such as the measles and borna

viruses.158-160 In fact, blocking certain of the glutamate receptors can prevent

brain damage by the measles virus, as well as other viruses.158 We also know

that the prognosis of spinal meningitis can be determined by the spinal fluid

glutamate levels, with high levels having the worst prognosis.161 Studies of

autistic children have also shown elevated glutamate levels in their blood and

spinal fluid.

 

Because excitotoxicity plays such an important role in autism, parents of

autistic children should avoid feeding their children foods containing

excitotoxic additives, such as MSG, hydrolyzed protein, vegetable protein

extracts, soy protein or soy protein isolate, natural flavoring, yeast enzymes,

etc. There are many disguised names for high glutamate food additives. A recent

study has also shown that there is an interaction between certain food dyes and

glutamate and aspartame that enhances neurotoxicity significantly.

 

They should also avoid immune suppressing oils, such as the omega-6 oils (corn,

soybean, peanut, safflower, sunflower and peanut oils). As stated, people in

this country eat 50-times the amount of this immune suppressing oil than they

need for health.

 

While omega-3 oils are healthy, the EPA component is significantly immune

suppressing and as a result, high intakes should be avoided. Studies have shown

suppressed lymphocyte function (NK cells) with high intake of EPA.162 It is the

DHA component that has most of the beneficial effects, especially as regards

brain repair and inflammation reduction.163 DHA also inhibits excitotoxicity.

Because the autistic child has intense brain inflammation, a combination of EPA

and DHA is preferable, with a lower content of EPA (no more than 250 mg).

 

Milk and milk products should be avoided and foods containing gliadin and gluten

should also be avoided. Soy foods are also responsible for a significant number

of food allergies as well as being very high in glutamate, fluoride and

manganese. Fluoride should be avoided, especially in drinking water. Water is

also a significant source of aluminum in the diet (it is added as a clarifying

agent) and in fluoridated water the fluoride complexes with aluminum to form the

highly neurotoxic fluoroaluminum compound. The greatest dietary source of

aluminum is biscuits, pancakes, black tea and baked goods made with

aluminum-containing baking powder.

 

Low magnesium intake, which is common in the United States, is associated with

higher degrees of inflammation in the body and lower glutathione levels. It also

enhances excitotoxicity, since magnesium is a natural modulator of the NMDA

glutamate receptor. Low intakes of magnesium greatly enhance glutamate receptor

sensitivity, worsening excitotoxicity. Low magnesium also lowers brain

glutathione levels, which increases brain sensitivity to mercury toxicity.

Increasing magnesium levels, reduces inflammation, raises glutathione levels and

reduces excitotoxic sensitivity.

 

A number of flavonoids are neuroprotective, especially against inflammation and

excitotoxicity. These include curcumin, quercetin, ellagic acid, natural vitamin

E (mixed trocopherol), epigallocatechin gallate (from white tea), theanine, DHEA

and hesperidin. All are available as supplements and most have a high safety

profile.

 

The live virus vaccines, such as chickenpox, measles, mumps and rubella, pose a

special danger in the immunosuppressed child, because some of these viruses can

take up permanent residence in the body, including the brain. In one study,

which examined the tissues of elderly dying of non-infectious causes, found live

measles virus in 45% of the bodies examined and 20% of their brains.164,165

These measles viruses were highly mutated, meaning they could result in a number

of diseases not normally suspected with measles infection.

 

I have omitted discussions about vaccine contamination, which is a major

problem. Several studies found a high incidence of microorganism contamination

in vaccines made by a number of major pharmaceutical companies, with figures as

high a 60% of the vaccines being contaminated.94-99 Bacterial and viral

fragments have also been found in a number of vaccines. While vaccine promoters

were quick to assure us that these viral fragments should cause no problem,

research says otherwise. In fact, a non-viable viral fragment implanted in

microglia and astrocytes in the brain causes the devastating dementia associated

with the HIV virus.167,168 The virus does not infect the brain neurons

themselves. The mechanism proposed is an immunological/excitotoxic-induced

toxicity, just as we see with repeated vaccination. The same mechanism is seen

with a number of viruses, including measles viruses, borna virus and the herpes

virus.168-172

 

When brain glial cells or neurons are chronically infected with these viruses

(called a persistent viral infection) the smoldering immune/excitotoxic reaction

slowly destroys the brain cell connections because the immune system is

attempting to destroy the infectious microorganism. Since it can never kill the

organism, the destruction (and intense microglial activation) continues for

decades, as we saw in the autistic brain.54 The same can occur with viral

fragments, the Lyme disease organism, aluminum and mercury that has accumulated

in the brain from either contaminated vaccines or from vaccine additives. And

because excessive vaccination, especially with immune-suppressive viruses, can

depress proper immune function, the child is at a greater risk of developing

such a persistent viral infection. Likewise, they are at a greater risk of

developing deadly invasive bacterial infections, such as H. Influenza

meningitis, pneumococcal and meningiococcal

meningitis. When it occurs, the vaccine promoters scream that we need more

vaccines to protect the children, never admitting that it was the vaccine

program itself that destroyed the lives of these children.

 

While a number of people and even physicians, think they desire a universal

health care system (a euphemism for socialized medicine), here is something to

consider. The government will use access to health care as a way to mandate

vaccinations for all Americans. Those who refuse any of the mandated vaccines

will be denied access to health care, meaning you will not be able to see a

doctor or enter a hospital or clinic.

 

All federal programs will have completion of vaccine mandates as a requirement.

This could be linked to social security, food stamps, housing subsidy programs

and other such federal programs. Remember, they use such tactics now for access

to schools and daycare centers. One may even have to prove that they have had

all their required vaccinations before they can use public transportation, such

as busses, trains and airplanes.

 

Another thing to consider is that the communist Chinese are gradually taking

over vaccine manufacturing. In fact, communist China is now the largest vaccine

manufacturer in the world . They have over 400 biopharmaceutical companies busy

making vaccines and poor quality drugs for the world. The FDA admits that it

inspects only 1.8% of the 714 drug firms in China and that, according to a GAO

study, that FDA inspections may be 13 years apart (it is spaced 2 years apart in

the United States).

 

Even more frightening is that the inspectors must depend on Chinese translators

and US companies purchasing these vaccines and pharmaceuticals must, by

agreement, have a Chinese communist official serve as its legal representative.

According to the Phyllis Schafly Report, one CEO was quoted as saying “ every

piece of information you get (from the Chinese) is suspect.â€

 

With thousands of people dying and getting sick, not only in China, but in

hundreds of nations receiving their tainted pharmaceutical products, this means

future vaccines will be an even greater danger. The risk of millions of

Americans and others living in the West receiving contaminated vaccines is

extremely high. It could even be done on purpose, since the Chinese communist

have declared their intention to defeat the United States. Infecting over a

hundred million Americans with contaminated vaccines would be an easy way to

defeat us. The irony would be that our public officials would have aided them in

our destruction.

 

Parents must appreciate that those in positions of authority are lying to them.

Most pediatricians think they are doing what is right, because they too are

victims of years of propaganda by elite members in the CDC and American Academy

of Pediatrics. Most truly believe what they are telling parents. They should

wake up and joint the fight to bring some sense to this insane policy.

 

 

 

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