What They Don't Tell You About Vaccination Dangers Can Kill You or Ruin Your Lif

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What They Don't Tell You About Vaccination Dangers Can Kill You or Ruin Your

Life

By L. Blaylock, M.D.

Advanced Nutritional Concepts, LLC

_www.russellblaylockmd.com_ (http://www.russellblaylockmd.com/)

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After 30 years of intensive research, much has been learned about how brain

cells work and what goes wrong when disease arises. One of the great enigmas

has been the connection between vaccinations and certain brain disorders such

as:

* Autism

* ADD

* ADHD

* Gulf War Syndrome

More common neurodegenerative diseases (Parkinson's disease, Alzheimer's

dementia and ALS)

As we learned more and more about how brain cells should work, we discovered

that often normal processes, such as metabolism, could result in the

accumulation of powerful chemical byproducts, called free radicals, that have

the

capacity to destroy these cells.

Free radicals, basically, are very reactive particles that bounce all around

the cell damaging everything they touch. Most originate during the process

of metabolism but can also arise from toxin exposure, irradiation and toxic

metals. Because they are so destructive, cells have a network of defenses

designed to neutralize them. This antioxidant network is composed of numerous

components that include vitamins, minerals and special chemicals called thiols

(glutathione and alpha-lipoic acid).

What Causes the Free Radicals

The idea that free radicals play a major role in all of the conditions

listed above is now proven--the big question is why are so many free radicals

being generated? In the case of autism, ADD and ADHD many came to support the

idea that mercury derived from vaccines was the source of the radicals. And it

was known that mercury could cause free radicals to be generated in large

numbers within the brain. Evidence connecting mercury to the autism spectrum

disorders, neurodegeneration and the Gulf War Syndrome is strong, but not

exclusive.

Interestingly, all of these diseases also share another common event--over

activation of a portion of the immune system.

It is important to appreciate that only a certain part of the immune system

is overactive, because other parts, such as cellular immunity, are actually

diminished. In some instances, as with the childhood disorders, the problem is

congenital and in others it develops as a result of many factors such as

aging, toxin exposure, poor nutrition and excessive vaccination itself. Mercury

can impair immune function as well.

How Vaccines are Made

Basically, vaccines contain either killed viruses or bacteria, germ

components, toxic extracts or live organisms that have been made less

virulent--a

process called attenuation. To stimulate an enhanced immune reaction against

these organisms, manufacturers added powerful immune-stimulating substances

such

as squalene, aluminum, lipopolysacchride, etc. These are called immune

adjuvants.

The process of vaccination usually required repeated injections of the

vaccine over a set period of time. The combination of adjuvants plus the

intended

organism triggers an immune response by the body, similar to that occurring

with natural infections, except for one major difference. Almost none of these

diseases enter the body by injection. Most enter by way of the mucous

membranes of the nose, mouth, pulmonary passages or GI tract. For example,

polio is

known to enter via the GI tract. The membranes lining these passages contain

a different immune system than activated by direct injection. This system is

called the IgA immune system.

It is the first line of defense and helps reduce the need for intense

activation of the body's immune system. Often, the IgA system can completely

head

off an attack. The point being that injecting organisms to induce immunity is

abnormal.

Because more and more reports are appearing citing vaccine failure, their

manufacturers' answer is to make the vaccines more potent. They do this by

making the immune adjuvants more powerful or adding more of them. The problem

with this approach is that in the very young, the nutritionally deficient and

the aged, over-stimulating the immune system can have an opposite effect--it can

paralyze the immune system.

This is especially prevalent with nutritional deficiency.

An early attempt to vaccinate Africans met with disaster when it was

discovered that many were dying following vaccination. The problem was traced

to

widespread vitamin A deficiency among the tribes. Once the malnutrition was

corrected, death rates fell precipitously.

Another problem we see with modern vaccines is that the immune stimulation

continues over a prolonged period of time.

This is because of the immune adjuvants. They remain in the tissues,

constantly stimulating immune-activating cells. With most natural infections the

immune activation occurs rapidly, and once the infection is under control, it

drops precipitously. This, as we shall see, is to prevent excessive damage to

normal cells in the body.

What Happens to the Brain With Vaccination?

It seems the brain is always neglected when pharmacologists consider side

effects of various drugs. The same is true for vaccinations. For a long time no

one considered the effect of repeated vaccinations on the brain.

This was based on a mistaken conclusion that the brain was protected from

immune activation by its special protective gateway called the blood-brain

barrier. More recent studies have shown that immune cells can enter the brain

directly, and more importantly, the brain's own special immune system can be

activated by vaccination.

You see, the brain has a special immune system that operates through a

unique type of cell called a microglia.

These tiny cells are scattered throughout the brain, lying dormant waiting

to be activated. In fact, they are activated by many stimuli and are quite

easy to activate. For our discussion, activation of the body's immune system by

vaccination is a most important stimuli for activation of brain microglia.

Numerous studies have shown that when the body's immune system is activated,

the brain's immune cells are likewise activated. This occurs by several

pathways, not important to this discussion. The more powerfully the body's

immune

system is stimulated the more intense is the brain's reaction. Prolonged

activation of the body's immune system likewise produces prolonged activation

of

the brain's immune system.

Therein lies the danger of our present vaccine policy.

The American Academy of Pediatrics and the American Academy of Family

Practice have both endorsed a growing list of vaccines for children, even

newborns,

as well as yearly flu shots for both children and adults. Children are

receiving as many as 22 inoculations before attending school.

What Happens When the Brain's Immune System is Activated?

The brain's immune system cells, once activated, begin to move about the

nervous system, secreting numerous immune chemicals (called cytokines and

chemokines) and pouring out an enormous amount of free radicals in an effort to

kill invading organisms. The problem is--there are no invading organisms. It

has

been tricked by the vaccine into believing there are.

Unlike the body's immune system, the microglia also secrete two other

chemicals that are very destructive of brain cells and their connecting

processes.

These chemicals, glutamate and quinolinic acid, are called excitotoxins. They

also dramatically increase free radical generation in the brain. Studies of

patients have shown that levels of these two excitotoxins can rise to very

dangerous levels in the brain following viral and bacterial infections of the

brain. High quinolinic acid levels in the brain are thought to be the cause of

the dementia seen with HIV infection.

The problem with our present vaccine policy is that so many vaccines are

being given so close together and over such a long period that the brain's

immune system is constantly activated. This has been shown experimentally in

numerous studies. This means that the brain will be exposed to large amounts of

the excitotoxins as well as the immune cytokines over the same period.

Studies on all of these disorders, even in autism, have shown high levels of

immune cytokines and excitotoxins in the nervous system. These destructive

chemicals, as well as the free radicals they generate, are diffused throughout

the nervous system doing damage, a process called bystander injury. It's sort

of like throwing a bomb in a crowd.

Not only will some be killed directly by the blast but those far out into

the radius of the explosion will be killed by shrapnel.

Normally, the brain's immune system, like the body's, activates quickly and

then promptly shuts off to minimize the bystander damage. Vaccination won't

let the microglia shut down. In the developing brain, this can lead to language

problems, behavioral dysfunction and even dementia.

In the adult, it can lead to the Gulf War Syndrome or one of the more common

neurodegenerative diseases, such as Parkinson's disease, Alzheimer's

dementia or Lou Gehrig's disease (ALS).

A recent study by the world-renowned immunologist Dr. H. Hugh Fudenberg

found that adults vaccinated yearly for five years in a row with the flu

vaccine

had a 10-fold increased risk of developing Alzheimer's disease. He attributes

this to the mercury and aluminum in the vaccine. Interestingly, both of

these metals have been shown to activate microglia and increase excitotoxicity

in

the brain.

Direct Effect of the Cytokines

Various cytokines have been used to treat cancer patients as well as other

common diseases.

Studies of the effects of these cytokines on brain function reveal some very

close parallels to the diseases we have been discussing. For a more in-depth

study of these effects I suggest you read my article appearing in the

Journal of the American Nutriceutical Association (volume 6 [fall], Number 4,

2003,

pp 21-35) and in the summer issue 2004 of the Journal of the American

Association of Physicians and Surgeons.

One can see:

* Confusion

* Language difficulties

* Disorientation

* Seizures

* Memory problems

* Somnolence

* Low-grade fevers

* Irritability

* Mood alterations

* Combativeness

* Difficulty concentrating

* A host of other behavioral problems

In the child, brain immune over-activation has been shown to be particularly

damaging to the amygdala and other limbic structures of the brain. This can

lead to unusual syndromes such as the loss of " theory of mind " and " Alice in

Wonderland syndrome. " It has also been shown to damage the executive

functions of the frontal lobes.

In essence, what is lost is that which makes us social human beings, able to

function in a complex world of ideas and interactions.

Several studies have indeed shown elevated levels of cytokines in autistic

children. It is also interesting to note that these cytokines, especially

interleukin-1ß and tumor necrosis factor-alpha (TNF-a) dramatically increase

the

damage produced by excitotoxins. So, what we see is a viscous cycle of immune

activation, excitotoxin and cytokine excretion, and free radical production.

The latter starts the cycle all over again.

The Role of Autoimmunity and Viral Persistence

Studies in autistic children have shown that a state of immune attack on the

brain is occurring. Similar findings are seen with neurodegenerative diseases

and the Gulf War Syndrome. It must be appreciated that this autoimmunity was

triggered by the vaccinations and by organisms contaminating the

vaccinations. Once started, the immune reaction cannot stop, thus triggering

all the

destructive reactions I have discussed.

Dr. Garth Nicolson has shown a direct connection between mycoplasma

contamination of vaccines and the 200 percent increased incidence of ALS in

Gulf War

veterans. The disorder is produced by the same mechanism described above.

Another, even more common, problem is the use of live viruses in vaccines.

The reason live viruses can be used is that they are weakened by passing them

through a series of cultures--a process called attenuation. These attenuated,

non-disease-causing viruses are then injected in hopes of stimulating the

body to produce an immune attack.

The problem with this idea is two-fold.

First, we now know that in far too many cases these virus

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system and take up residence in the body--for a lifetime. A recent autopsy

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of elderly individuals found that 20 percent of the brains contained live

measles virus

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identical genetically to the one used in the vaccine.

The second problem is that most of these viruses were found to be highly

mutated. In fact, different mutations were found among viruses in various

organs

in the same individual.

This has been a secret kept from the public.

These attenuated viruses undergo mutation brought on by the presence of free

radicals in the tissues and organs and they can mutate into virulent,

disease-causing organisms. Recent studies have confirmed this frightening

finding.

In fact, a large percentage of Alzheimer's disease patients have live viruses

in their brain as compared to normal individuals.

Once these live virus

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in the body, they will be under constant free radical exposure, which can

increase during times of stress, illness, exercise and with aging. It is the

free

radicals that cause the virus

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In essence, the virus

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slowly producing destruction of the brain or spinal cord or producing sudden

disease once the virus

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Conclusions

We have seen that the policy of giving numerous vaccinations to individuals,

especially infants and small children, is shear idiocy.

A considerable number of studies have shown conclusively that such a

practice can lead to severe injury to the brain by numerous mechanisms. Because

the

child's brain is undergoing a period of rapid growth from the third trimester

of pregnancy until age 2 years, his or her brain is at considerable risk

from this insane policy.

We have also seen that live-virus vaccines and contaminated vaccines hold a

special risk in that the viruses tend to persist in a substantial number of

individuals and that free radicals can cause the latent viruses to transform

by genetic mutation into disease-causing organisms later in life.

It is vital that anyone scheduled for vaccination follow a schedule that

allows no more than one vaccine every six months, allowing the immune system

time to recover.

Live-virus vaccines should be avoided.

This was recently illustrated by the switch from the live polio vaccine to

the killed virus. All cases of polio after the introduction of the vaccine, in

the developed world, came from the vaccine itself. This was known from the

beginning.

Finally, it is vital that anyone undergoing vaccination should start

nutritional supplementation and adhere to a healthy diet before vaccination

occurs.

Vaccine complications are far fewer in individuals with good nutrition.

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