AUTISM PREVENTION FATHER BABIES 24-34 PATERNAL AGE IS KEY IN NON-FAMILIAL AUTISMVaccines

"It is very possible that PATERNAL AGE is the major predictor of(non-familial) autism." Harry Fisch, M.D., author "The Male Biological Clock". Sperm DNA mutates and autism, schizophrenia bipolar etc. results. What is the connection with autoimmune disorders? Having Type 1 diabetes, SLE,etc. in the family, also if mother had older father. NW Cryobank will not accept a sperm donor past 35th BD to minimize genetic abnormalities.VACCINATIONS also cause autism.

Saturday, September 12, 2009

FLU SHOTS AND THE NEW ADJUVANTS: BEWARE

Ingredients Found in Spermicides, Cleaners, and Cosmetics along with Thimerosal, and Squalene Present in Experimental H1N1 Vaccine

Jeffry John Aufderheide
VacTRUTH
09/11/09

See for yourself the study presented at the end of article. Please spread the word and make this go viral… no pun intended. Kindly reference and link to VacTRUTH!

(vactruth.com) Trials for the experimental H1N1 Swine flu vaccine commence Tuesday, September 15th in Thornton, Colorado. Novartis, a bio-pharmaceutical company that manufactures the vaccine, is recommending that children participating in the trial receive two doses of an experimental vaccine which contain ingredients found in spermicides, cleaners, and cosmetics along with thimerosal and squalene (MF59). Everyone should have a sense of concern as the only safety checks for these children are a few blood draws and follow-up phone calls. No neurological testing. No kidding.

Official opinions from federal agencies, such as the CDC, insist that the new vaccine will be safe and effective. Experts say we can trust the new H1N1 experimental vaccine because the technology used to create the vaccine is time tested. Experts argue that the only variable changing from the ‘normal’ flu vaccine and the H1N1 experimental vaccine is the novel A/H1N1 antigen. In other words, the same vaccine ‘technology’ is used but with the new virus.

However, this is the furthest thing from the actual TRUTH. As will be demonstrated, the following information was obtained through enrolling a family member into the study to gain an understanding as to what the ingredients would be. After finding out the the information I am about to share, enrollment in this trial has been canceled.



SETTING THE STAGE ON SAFETY AND SQUALENE (MF59)

I met with the research coordinator for the study along with Dr. Melamed, an immunologist conducting the study. Dr. Melamed altruistically shared his knowledge answering questions concerning immunology and the technology behind the vaccine while remaining evasive on questions of what was in the vaccine and legal ramifications if harm was done. Dr. Melamed reassured me several times that the experimental H1N1 vaccine was created just like past vaccines and that the technology was well established.

Requests for package inserts for the ingredients of the experimental H1N1 vaccine were denied on the grounds that this was a study and that information is privileged. However, we can still piece together some of the ingredients based upon the parental consent form.

“MF59 is an adjuvant which is used in influenza vaccines licensed for the adults and/or elderly in many countries worldwide, but it is not contained in any vaccines currently approved in the United States.” (page 2)

Isn’t it interesting that the study states it is licensed for adults and elderly? This study is designed for children between the ages of 3 and 8 and they plan on shooting up newborns and pregnant women with this stuff? Buyer beware.

Here is what the World Association for Vaccine Education had to say about Squalene (MF59):

Squalene:C30H50 an Adjuvant


Too dangerous for human use, Squalene is not licensed for use in the United States. Oil adjuvants like squalene have been ordinarily used to inflict diseases in animals – for experimentation and study. According to anthrax vaccine expert Gary Matsumoto and other reliable sources, the US military used an unlicensed, experimental anthrax vaccination laced with squalene, with disastrous consequences, including Gulf War Sydrome. Chemical descriptions:
Unites States National Library of Medicine: PubChem
http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=638072
Toxicity:
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?CMD=search&DB=pubmed&term=%22Squalene%2ftoxicity%22[Mesh%20Terms%3anoexp

Adverse effects:
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?CMD=search&DB=pubmed&term=%22Squalene%2fadverse%20effects%22[Mesh%20Terms%3anoexpMust read:
Matsumoto, Gary. Vaccine A; The Covert Government Experiment That's Killing Our Soldiers – and Why GI's Are Only the First Victims. Basic Books, 2004.
Present in these vaccines:
Anthrax (experimental, used on military personnel)

Dr. Sherri Tenpenny also elaborates on the deleterious effects of the Squalene Adjuvant in a 2006 article entitled, "FLU SHOTS AND THE NEW ADJUVANTS: BEWARE!" and can be found in its entirety here. An excerpt from Dr. Tenpenny's article can give a better appreciation and understanding of what squalene is capable of in the body...

"On first blush, squalene seems like a good choice for an adjuvant. Manufactured naturally in the liver, squalene is a precursor for cholesterol. In addition, squalene can be purchased at health food stores in its more commonly known form, “shark liver oil.” However, ingested squalene has a completely different effect on the body than injected squalene. When molecules of squalene enter the body through an injection, even at concentrations as small as 10 to 20 parts per billion, it can lead to self-destructive immune responses, such as autoimmune arthritis and lupus.

Several mechanisms have been proposed to explain this reaction. Metabolically, squalene stimulates an immune response excessively and nonspecifically. More than two dozen peer-reviewed scientific papers from ten different laboratories throughout the U.S., Europe, Asia, and Australia have been published documenting the development of autoimmune disease in animals subjected to squalene-based adjuvants. A convincing proposal for why this occurs includes the concept of “molecular mimicry” in which an antibody created against the squalene in MF59 can cross react with the body’s squalene on the surface of human cells. The destruction of the body’s own squalene can lead to debilitating autoimmune and central nervous system diseases."

“Carcinogenicity, we (Dr. Deborah Novicki of Novartis, another pharmaceutical company) have done no testing for the carcinogenicity of MF59 adjuvant or any of our preventive vaccines. We haven’t done it and we don’t plan to.”

This information is found on a workshop on adjuvants and adjuvanted preventative and therapeutic vaccines hosted by the FDA. This gem of a quote is on page 391.




STRANGE BEDFELLOWS: THIMEROSAL AND SPERMICIDES

Further down we see that, while not mentioned explicitly as ingredients, one can deduce they are in the vaccine via an implied allergic reaction.

"If your child has had an allergic reaction in the past to eggs, egg products, neomycin or polymyxin (antibiotics), sodium ethylmercurothiosalicylate or thimerosal (compounds containing mercury that are frequently used as preservatives in vaccines), beta propriolactone (substance that inactivates a virus), or nonoxynol 9 (substance commonly used in cleaners, cosmetics, and spermicides), you must tell the medical staff..." (pg 8) (emphasis mine)

Thimerosal has been thoroughly exposed as a neurological toxin largely in part and much gratitude to Lyn Redwood who obtained the meeting minutes from a secret meeting between government officials and pharmaceutical companies discussing the effects of the mercury additive. The document is called the Simpsonwood document and details exclusively the neurological harm thimerosal causes in children. Dr. Russell Blaylock has a commentary on the document here or read the meeting minutes yourself here.

“the number of dose related relationships [between mercury and autism] are linear and statistically significant. You can play with this all you want. They are linear. They are statistically significant.” – Dr. William Weil, American Academy of Pediatrics. Simpsonwood, GA, June 7, 2000

“the issue is that it is impossible, unethical to leave kids unimmunized, so you will never, ever resolve that issue [regarding the impact of mercury].” – Dr. Robert Chen, Chief of Vaccine Safety and Development, Centers For Disease Control, Simpsonwood, GA, June 7, 2000

“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.” – Dr. Robert Johnson, Immunologist, University of Colorado, Simpsonwood, GA, June 7, 2000

“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…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.” – Dr. John Clements, World Health Organization, Simpsonwood, GA, June 7, 2000

One can only wonder the harmful effects nonoxynol 9 could bring. I could find no past flu vaccine that contained this ingredient nor study showing it is safe to inject into humans.

At this point, it must be said. According to the CDC’s vaccine schedule, children now receive 36 vaccines prior to going into kindergarten. This fall season will add 4 additional vaccines to this total for a grand total of 40!? And we’re not even getting warmed up…

POSSIBLE RISKS AND SIDE EFFECTS

By far the most entertaining part of the meeting with Dr. Melamed is when my eyes bugged out on page 6 and 7 of the study. It was explained to me that the side effects I am about to list off are side effects for all vaccines… and that I had nothing to worry about because this vaccine, this vaccine as you recall was made with ‘established technology’. If that is the case, it is the cause for even MORE concern!!!!

“Other side effects that have been reported in clinical studies with other influenza vaccines or have been reported by people who received influenza vaccines may include: [VacTRUTH Editor's Note: Potential Flu Symptoms Highlighted in RED]


Reactions at the site of injection:

bruising
itchiness
rash
warmth
lump or irritation at the site where the vaccine was given
sharp pain in or along nerves or tingling of pins and needles (paresthesia)
pain limiting movement of the limb where the vaccine was given
infection
muscle ache
Other general reactions:

hot flashes or flushing
chills or shivering
dizziness
generalized weakness
fainting shortly after vaccination
nausea
vomiting
diarrhea
loss of appetite
abdominal pain
back pain
lymph node enlargement
temporary decrease in the number of blood platelets, which may increase the risk of bleeding
bleeding
decrease in red blood cells, or anemia, which may make you feel tired.
high blood pressure (hypertension)
shortness of breath
wheezing
chest tightness
chest pain
cough
sore throat
runny nose
“pins and needles” in the skin
sweating
skin disorders related to allergic reaction (which can lead to rash and skin loss)
inflammation of blood vessels (including inflammation of blood vessels that may cause short-term effect on kidneys)
confusion
headaches similar to those described as migraine
seizures associated with fever
spinal cord or brain inflammation (encephalomyelitis)
paralysis
muscle weakness
infection
life-threatening and/or debilitating disorders of the nervous system“
On IMMUNoE’s website, on page three of this flier, it states:

“Q: Could the new H1N1 vaccine cause a person to get the flu?

A: Contrary to popular belief, it is not possible to get flu from a flu vaccine. This is true for the seasonal flu vaccine, as well as the investigational(sic) H1N1 vaccine.”

Are the vaccines the same or not the same? Of course, Dr. Melamed at this point tells me about how people with weakened or no immune system can actually get the disease from a vaccine. I asked what measures were being used to understand what the child’s immune response would be (or even if they had an immune response to indicate it was working PRIOR to the vaccine) and Dr. Melamed said, ‘none’. If they don’t measure before and after, how will they know?


“These other general conditions have occurred in people who received influenza vaccines:

autoimmune disorders (these are disorders in which the body’s tissue are attacked by its own immune system and include liver injury or nerve injury)
arthritis (joint pain)” (pg 8)
DR ANDREW MOULDEN AND NEUROLOGICAL TESTING

Being a concerned parent one at this point would probably want to know how neurological damage is measured to know if it has occurred in their child. To my surprise, NO NEUROLOGICAL MEASUREMENTS are taken!!! Neurological damage can clearly be seen in past flu vaccines as was the case in the 1975-76 swine flu vaccine.

Dr. Andrew Moulden gives laypersons clinical skills to detect neurological damage occurring after a child or adult is vaccinated. I highly recommend his DVD – Tolerance Lost that is found on his Brainguard website or reading several articles posted exclusively on VacTRUTH which will give you these skills. They are respectively entitled, “Dr. Andrew Moulden (Interview): What You Were Never Told About Vaccines” and “Vaccinations are causing impaired blood flow (Ischemia), Chronic Illness, Disease and Death for us all“. The second article has photographs showing you precisely what is occurring.

In a separate interview with Dr. Moulden, he succinctly states that if neurological measures are never taken, the industry can say that vaccines are safe.

The only measurements taken will be a brief physical exam, measurement of vital signs and body temperature, blood samples to check for immune response, reviewing diaries with staff, and follow up phone calls. (pg4) Monitoring for safety is occurring for 13 months. How can, then, the vaccines be declared for public use with any certainty of safety in less than 2 months?

“It is also of the understanding that eight investigational (sic) vaccine formulations with different amounts of A/H1N1 antigens and with or without adjuvant will be tested for this study.” (pg 2)

OVERVIEW

Let us recap.
1. The vaccine contains squalene (MF59) which has not been tested for causing cancer.
2. The vaccine contains thimerosal, a known culprit in causing autism and neurological deficits.
3. The vaccine curiously contains nonoxynol-9 used in spermicides.
4. The vaccine will likely cause (and spread) the flu.
5. No neurological testing will be done to ensure the vaccine is safe from harmful neurological side effects.
6. Monitoring for safety will last 13 months, well beyond the flu season.

As to my knowledge, this information is the first of its kind validating the ingredients and the intent to use them on the population. Buyer beware of this vaccine as we are likely to see an onslaught of damaged men, women, and children if there are forced vaccines. The ‘new’ experimental vaccine is certainly unlike any other that we, as Americans, have been exposed to in the past.



Vaccine Trial Paperwork



--------------------------------------------------------------------------------
VacTRUTH Editor’s Note:

1. Check out Jonathan Elinoff’s new website http://vaccinationeducation.com.

2. Dr. Sherri Tenpenny has a great site to educate yourself on the upcoming flu season at http://pandemicfluonline.com.

3. Dr. Mayer Eisenstein has a free webinar series talking about various topics in vaccinology. Visit his website at http://homefirst.com.

4. Read how pharmaceutical companies plan on superseding parental consent laws to force mass vaccinations here.

5. Visit InTheory.tv for interviews I have done concerning vaccines with Chris Yankowski.

FLU SHOTS AND THE NEW ADJUVANTS: BEWARE!

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Sunday, September 06, 2009

FLU SHOTS AND THE NEW ADJUVANTS: BEWARE

FLU SHOTS AND THE NEW ADJUVANTS: BEWARE!Dr. Sherri Tenpenny, DO - May 1, 2006 First published at: NewsWithViews.com"Multiple studies published in highly reputable publications have documented that flu shots are ineffective in all ages." "..., one adjuvant has been approved in Europe and its approval is on the way for use in the U.S. It is an oil-based adjuvant called MF-59, a compound primarily composed of squalene." Read whole story at: NewsWithViews.com

A Glimpse into the Scary World of Vaccine AdjuvantsBy Edda West - Published in VRAN Newsletter - Winter 2005 Vran.org contact link is at the bottom of their home page. www.vran.org
Adjuvants are formulated compounds, which when combined with vaccine antigens intensify the body's immune response. They are used to elicit an early, high and long-lasting immune response. "The chemical nature of adjuvants, their mode of action and their reactions (side effect) are highly variable in terms of how they affect the immune system and how serious their adverse effects are due to the resultant hyperactivation of the immune system. While adjuvants enable the use of less *antigen to achieve the desired immune response and reduce vaccine production costs, with few exceptions, adjuvants are foreign to the body and cause adverse reactions", writes Australian scientist Viera Scheibner Ph.D, (1)
The most common adjuvant for human use is an aluminum salt called alum derived from aluminum hydroxide, or aluminum phosphate. A quick read of the scientific literature reveals that the neurotoxic effects of aluminum were recognized 100 years ago. Aluminum is a neurotoxicant and has been linked to Alzheimer's disease and other neurological disorders. Prior to 1980, kidney patients undergoing long term dialysis treatments often suffered dialysis encephalopathy syndrome, the result of acute intoxication by the use of an aluminium-containing dialysate. This is now avoided using modern techniques of water purification. In preterm infants, prolonged intravenous feeding with solutions containing aluminum is associated with impaired neurologic development. Scientists speculate that aluminum neurotoxicity may be related to cell damage via free radical production, impairment of glucose metabolism, and effects on nerve signal transduction. (2) Vaccines which contain both aluminum adjuvants and mercury based preservative, greatly magnify the neurotoxic effects. (3)
Macrophagic myofasciitis (MMF) is a muscle disease first identified in 1993, and has been linked to vaccines containing aluminum adjuvants. Muscle pain is the most frequent symptom which can be localized to the limbs or be more diffuse. Other symptoms include joint pain, muscle weakness, fatigue, fever, and muscle tenderness. The disorder is associated with an altered immune system in some, but not all patients. A study published in the journal Brain (2001) revealed that 50 out of 50 patients had received vaccines against hepatitis B virus (86%), hepatitis A virus (19%) or tetanus toxoid (58%), 3-96 months (median 36 months) before biopsy. "We conclude that the MMF lesion is secondary to intramuscular injection of aluminium hydroxide-containing vaccines, shows both long-term persistence of aluminium hydroxide and an ongoing local immune reaction, and is detected in patients with systemic symptoms which appeared subsequently to vaccination", write the authors of the study. (4)
But aluminum's neurotoxicity is of less concern to the vaccine industry than the fact that it elicits a lesser antibody response to the so called purer recombinant or synthetic antigens used in modern day vaccines than in older style live or killed whole organism vaccines. "This has created a major need for improved and more powerful adjuvants for use in these vaccines." (5)
For decades, vaccine developers have been tinkering with various substances to trick the body into heightened immune responses. The most effective adjuvants are formulated with oils but have long been considered too reactive for use in humans. Immunologists have known for decades that a microscopic dose of even a few molecules of adjuvant injected into the body can cause disturbances in the immune system and have known since the1930's that oil based adjuvants are particularly dangerous, which is why their use has been restricted to experiments with animals.
The classic oil based adjuvant called Freund's Complete Adjuvant can cause permanent organ damage and irreversible disease - specifically autoimmune diseases. When scientists want to induce autoimmune disease in a lab animal, they inject it with Freund's Complete Adjuvant, which causes great suffering and is considered by some too inhumane to even inject into animals.
Dr. Jules Freund creator of this oil based adjuvant warned in 1956 that animals injected with his formulation developed terrible, incurable conditions: allergic aspermatogenesis (stoppage of sperm production), experimental allergic encephalomyelitis (the animal version of MS), allergic neuritis (inflammation of the nerves that can lead to paralysis) and other severe autoimmune disorders. (6)
Adjuvants can break "tolerance", meaning they can disable the immune system to the degree that it loses its ability to distinguish what is "self" from what is foreign. Normally, the immune system ignores the constituents of one's own body. Immunologists call this "tolerance". But if something happens to break "tolerance", then the immune system turns relentlessly self-destructive, attacking the body it is supposed to defend. (6)
Scientists theorize that oil based adjuvants have the ability to "hyperactivate" the immune system, and in doing so, create chaos by inducing such an extremely powerful response that the immune system literally goes haywire and starts attacking elements it would normally ignore. (6)
Another theory has to do with "specificity". One of the great distinguishing characteristics of the immune system is something akin to a highly sensitive innate intelligence that has evolved over eons to be able to respond very precisely to what it deems to be a threat to the body. Because the body contains many types of oily molecules and lipids, it may be that when an oil is injected, the immune system responds to it not only specifically, but with heightened intensity because the oil adjuvant resembles so closely the natural oils found in the body. A "cross reaction" then happens, sending the immune system into chaos destroying any oils found anywhere in the body that resemble the adjuvant oil. Demyelinating diseases like multiple sclerosis are an example of this destructive autoimmune process. (6)
To deepen one's understanding of the shadowy world of vaccine development, award winning investigative journalist Gary Matsumoto's new book is a "must read." It documents the secret human medical experimentation conducted on American citizens by doctors and scientists working for the U.S. military. It is a book about "betrayal of the most fundamental rules of medical ethics; and betrayal of the basic duty of military and civilian leaders to protect the people they govern." Vaccine A: The Covert Government Experiment That's Killing our Soldiers and Why GI's are Only the First Victims, is a gripping read into the mad science world of the U.S. military's biowarfare vaccine development program which, since 1987 has injected tens of thousands of U.S. troops with an experimental unlicensed anthrax vaccine containing squalene. An oil based adjuvant, squalene has been known for decades to cause severe autoimmune diseases in laboratory animals. Writes Matsumoto, "The unethical experiments detailed in this book are ongoing, with little prospect of being self-limiting because they have been shielded from scrutiny and public accountability by national security concerns." Reading this book, one gets a permanent chill in the spine as we glimpse the "writing on the wall" of what is to come. (6,7)
"When UCLA Medical School's Michael Whitehouse and Frances Beck injected squalene combined with other materials into rats and guinea pigs back in the 1970's, few oils were more effective at causing the animal versions of arthritis and multiple sclerosis", writes Matsumoto. In 1999, Dr. Johnny Lorentzen, an immunologist at Sweden's Karolinska Institute proved that on injection, "otherwise benign molecules like squalene can stimulate a self-destructive immune response", even though they occur naturally in the body. Other research institutes have also shown that the immune system makes antibodies to squalene, but only after it is injected (6) We now know that squalene, added to boost immune response in a formulation known as MF59, is the secret ingredient in certain lots of experimental anthrax vaccine that has caused devastating autoimmune diseases and death in countless Gulf War vets (Canadian, British and Australian troops were also injected with squalene laced vaccine), and continues to be used today. There is a "close match between the squalene-induced diseases in animals and those observed in humans injected with this oil: rheumatoid arthritis, multiple sclerosis and systemic lupus erythematosus", writes Matsumoto. These three illnesses have been proven to be caused by this oil, but there is an additional long list of autoimmune diseases associated with squalene injection into humans. (6) "There are now data in more than two dozen peer-reviewed scientific papers, from ten different laboratories in the U.S., Europe, Asia and Australia, documenting that squalene-based adjuvants can induce autoimmune diseases in animals..observed in mice, rats, guinea pigs and rabbits. Sweden's Karolinska Institute has demonstrated that squalene alone can induce the animal version of rheumatoid arthritis. The Polish Academy of Sciences has shown that in animals, squalene alone can produce catastrophic injury to the nervous system and the brain. The University of Florida Medical School has shown that in animals, squalene alone can induce production of antibodies specifically associated with systemic lupus erythematosus", writes Matsumoto. (6)
Long List of Side Effects Referring to squalene in her extensive article on adjuvants, Dr. Scheibner writes, "This adjuvant contributed to the cascade of reactions called "Gulf War syndrome", documented in the soldiers involved in the Gulf War. The symptoms they developed included arthritis, fibromyalgia, lymphadenopathy, rashes, photosensitive rashes, malar rashes, chronic fatigue, chronic headaches, abnormal body hair loss, non-healing skin lesions, aphthous ulcers, dizziness, weakness, memory loss, seizures, mood changes, neuropsychiatric problems, anti-thyroid effects, anaemia, elevated ESR (erythrocyte sedimentation rate), systemic lupus erythematosus, multiple sclerosis, ALS (amyotrophic lateral sclerosis) also known as Lou Gehrig's disease, Raynaud's phenomenon, Sjorgren's syndrome, chronic diarrhoea, night sweats and low-grade fevers. (1)
Matsumoto punctuates his book with poignant interviews of military personnel who suffered many of these extreme and devastating syndromes, all of whom tested positive for anti-squalene antibodies which has become THE definitive marker for people who have been injected with this adjuvant and who have gone on to develop catastrophic diseases.
Immunologist, Dr. Pamela Asa was the first person to recognize that the autoimmune diseases she was seeing in military personnel mirrored those in experimental animals injected with oil formulated adjuvants. When she met a patient with similar autoimmune symptoms who had participated in an experimental herpes vaccine trial, who also knew he had been injected with MF59, a squalene adjuvant being used as a 'placebo' in that study, everything began to fall into place. Pam Asa contacted Dr. Robert Garry, a leading virologist at Tulane University Medical School, whose specialty is developing antibody tests and asked him to develop a test for the detection of anti-squalene antibodies - a test that ultimately became the most important forensic and diagnostic tool identifying patients whose autoimmune diseases followed injection with squalene laced anthrax vaccine. (6)
Juxtaposed to heart wrenching testimonies of shattered health and ruined lives is the military's defiant stonewall and denial that a squalene laced anthrax vaccine was injected into thousands of its people without their informed consent - this despite the fact that the FDA and independent researchers have tested and identified varying amounts of squalene in specific lots of the vaccine.
Even more stunning is the fact that by 1997, hundreds of millions of dollars had already been spent testing vaccines formulated with squalene adjuvants by leading research institutes like NIH (National Institutes of Health) who tested its efficacy in HIV vaccines, the National Cancer Institute who for nearly two decades conducted research with squalene-boosted vaccines, and the National Institutes of Allergy and Infectious Diseases (NIAID) had been testing it in animals since 1988 and began human clinical trials in1991. Nineteen of NIAID's 23 trials were for prototype HIV vaccines. Writes Matsumoto, " Squalene adjuvants are a key ingredient in a whole new generation of vaccines intended for mass immunization around the globe." (6)
Immune System Sees Squalene as an Enemy to Attack Researchers at Tulane Medical School and the Walter Reed Army Institute of Research "have both proven that the immune system responds specifically to the squalene molecule. Squalene's pathway through the body has been tracked with a radioactive tracer in animals by none other than Chiron, (well known flu vaccine manufacturer) and maker of MF59, the squalene-based adjuvant, now also a component of FLUAD, an Italian influenza vaccine. (6)
The immune system does in fact "see" squalene and recognizes it as an oil molecule native to the body. The key is "route of administration". As Gary Matsumoto says, "Squalene is not just a molecule found in a knee or elbow - it is found throughout the nervous system and the brain." When it is injected into the body, the immune system sees it as an enemy to be attacked and eliminated.(6)
As any immunologist will tell you, the way an antigen encounters the immune system makes all the difference. You can eat squalene - no problem as it is an oil the body can easily digest. But studies in animals and humans show that injecting squalene will "galvanize the immune system into attacking it, which can produce a self-destructive cross reaction against the same molecule in the places where it occurs naturally in the body - and where it is critical to the health of the nervous system." (6)
This phenomenon is also known as 'molecular mimicry', where the immune system forms antibodies against one of its own structures and will continue to attack the 'self' molecule in the body that resembles the one in the germ, or as is the case with squalene, an identical substance that is naturally present in the body. Once this self-destructive process begins, it never stops as the body continues to make the molecule the immune system is now trained to attack.
Another example involving autoimmune 'molecular mimicry' is when the immune system has been sensitized to attack myelin, the insulating fatty coating around nerve fibres which insures the smooth relay of nerve signals. The body would continue to make myelin in order to replenish and repair the protective sheath around its nerve endings. But says Matsumoto, "In the act of doing so, the body immunizes itself against itself, administering over and over again what amounts to a booster dose of something that the immune system now wants to get rid of. This vital constituent (myelin) is now the enemy, and the immune system is now programmed to obliterate it in an endless loop of self-destruction" - the process involved in MS (multiple sclerosis), and ALS (Lou Gehrig's disease).(6)

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