Adverse Vaccination Effects on Gulf War TroopsBefore deploying to the Persian Gulf in 1990 - 91 (and thereafter to the present), all US troops got a standard series of inoculations against infectious diseases - the same ones given to all US citizens traveling to the region. After arriving, 150,000 also got anthrax vaccinations and 8000 botulinum toxoid ones even though concerns were raised about adverse long-term health consequences.
A National Academy of Sciences' Institute of Medicine (IOM) study was conducted to assess them with results released in September 2000. In December 1997, the Department of Defense (DOD) announced that all US military forces would receive anthrax vaccinations. The Anthrax Vaccine Immunization Program (AVIP) began in March 1998 even though IOM found little published peer-reviewed scientific information on its safety.
In its study, IOM reported evidence of an association between vaccinations studied and transient acute common health effects, including redness, swelling, and fever commonly associated with other vaccinations. However, conclusive proof of long-term problems wasn't determined - likely because study findings were skewed not to find them. More on that below.IOM also studied botulinum toxoid vaccines and found evidence of an association between the vaccine and transient acute local and systemic effects similar to anthrax vaccinations.
Again, conclusive proof of long-term adverse health effects wasn't found - another very dubious conclusion as evidence below explains.Military personnel usually get multiple vaccinations. IOM studied their effects but didn't prove or disprove any long-term adverse effects. However several independent studies of British Gulf War veterans found some link between multiple vaccinations and later health problems.
Gary Matsumoto is a New York-based award-winning investigative journalist. His 2004 book, "Vaccine A: The Covert Government Experiment That's Killing Our Soldiers and Why GIs are Only the First Victims" took sharp issue with IOM results and the Pentagon's denial of Gulf War syndrome.Investigating the shadowy vaccination development world, he discovered US military-employed doctors and scientists conducted secret medical experiments on US citizens in violation of the Nuremberg Code and fundamental medical ethics.
For its part, Nuremberg established legal medical experimental standards now incorporated into ethical medical codes, including:
-- requiring voluntary consent of human subjects without coercion, fraud, deceit, and with full disclosure of known risks;-- experiments should avoid "all unnecessary physical and mental suffering and injury;"-- experiments should never be conducted if there's "an a priori reason to believe death or disabling injury will occur;"-- risk "should never exceed that determined by the humanitarian importance of the problem to be solved..;" and-- experiments should be terminated if there's reason to believe they'll cause "injury, disability, or death to the experimental subject."
According to Matsumoto, the Pentagon violated these and other standards, betrayed the troops, and the fundamental duty of military and civilian leaders to protect them. Since at least 1987, biowarfare development trumped the welfare of tens of thousands of GIs used as human guinea pigs for inoculation with experimental unlicensed anthrax vaccines containing squalene - an oil-based adjuvant (to enhance immunity) known for decades to cause severe autoimmune diseases in lab animals, yet administered involuntarily without disclosure of its harmful effects to human health. Matsumoto wrote:
"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."
He suggested the "writing (was) on the wall" of what's to come with prospects now it may be soon."When UCLA Medical School's Michael Whitehouse and Frances Beck injected squalene combined with other materials into rats and guinea pigs back in the 1970s, few oils were more effective at causing the animal versions of arthritis and multiple sclerosis."
In 1999, immunologist Dr. Johnny Lorentzen at Sweden's Karolinska Institute found that on injection, an "otherwise benign molecule like squalene can stimulate a self-destructive immune response," even though it occurs naturally in the body.Other research shows that squalene is the experimental anthrax vaccine ingredient that caused devastating autoimmune diseases and deaths for many Gulf War veterans from the US, UK, and Australia, yet it continues in use today and for new vaccines development in labs.
There's 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."Other autoimmune diseases are also linked to humans injected with squalene. "There are now data in more than two dozen peer-reviewed scientific papers, from ten different laboratories in the US, 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.
"Micropaleontologist Dr. Viera Scheibner conducted research into the adverse effects of adjuvants in vaccines and wrote:Squalene "contributed to the cascade of reactions called "Gulf War syndrome. (GIs developed) 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, Raynaud's phenomenon, Sjorgren's syndrome, chronic diarrhea, night sweats and low-grade fever."
Matsumoto's book includes numerous case studies of GIs afflicted with one or more of the above syndromes, their devastating effects, and the outlandish US government reaction - failing to acknowledge their existence or a connection between them and administered vaccines. Also denying the effects of other toxic Gulf theater exposures (like depleted uranium) as well as withholding meaningful treatments or protocols.US Army Captain George L. Skypeck spoke eloquently for many when he said:"Was the character of my valor less intense than those at Lexington? Was the pain of my wounds any less severe than those at Normandy? And was my loneliness any less sorrowful than those at Inchon? Then why am I forgotten amonst those remembered as 'heros?' "
If mass vaccinations are ordered, millions of Americans may ask: Why do you keep using unsafe vaccines and other drugs when clear evidence shows their dangers? Why do you jeopardize all Americans by unleashing a future plague of serious illnesses, diseases, and disabilities? Why have you willfully and maliciously ruined my health?Immunologist Dr. Pamela Asa first recognized autoimmune diseases showing up in GIs that mirrored those in lab animals injected with oil formulated squalene adjuvants.
By 1997, hundreds of millions of dollars had been spent testing vaccines containing them, in animal studies since 1988 and human clinical trials since 1991 - by leading research institutes like NIH, the National Cancer Institute, and the National Institutes of Allergy and Infectious Diseases (NIAID).According to Matsumoto, today, "Squalene adjuvants are a key ingredient in a whole new generation of vaccines intended for mass immunization around the globe" even though researchers at Tulane Medical School and the Walter Reed Army Institute of Research proved "that the immune system responds specifically to the squalene molecule."
The immune system "see(s) and recognizes it as an oil molecule native to the body. Squalene is not just a molecule found in a knee or elbow - it is found throughout the nervous system and the brain." When injected in the body, the immune system attacks it as an enemy to be eliminated. Eating and digesting squalene isn't a problem. But injecting it "galvanize(s) the immune system into attacking it, which can produce self-destructive cross reactions 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."Once self-destruction begins, it doesn't stop as the body keeps making the molecule that the immune system is trained to attack and destroy.
Immunologist Dr. Bonnie Dunbar also did extensive research on hepatitis B-inflicted illnesses and found similar autoimmune processes involved in molecular mimicry in people with devastating neuroimmune syndromes after getting vaccine injections.Matsumoto says "Squalene is a kind of trigger for (a) real biological weapon," what Soviet researchers called "a biological time bomb!!" and Matsumoto says is "the immune system." When its "full repertoire of cells and antibodies (attack) tissues they are supposed to protect, the results can be catastrophic."
He and Dr. Pam Asa conclude that "Oil adjuvants are the most insidious chemical weapon ever devised," including ones with squalene - something the Soviets knew could be used as a weapon in the 1980s.Matsumoto says that "the real problem with using squalene (isn't) that it mimics a molecule found in the body; it is the same molecule. So what American scientists conceived as a vaccine booster (or what's now being developed in labs) was another 'nano-bomb,' instigating chronic, unpredictable and debilitating disease.
When the NIH....argued that squalene would be safe because it is native to the body, just the opposite was true," and, of course, still is. "Squalene's natural presence in the body made it one of the most dangerous molecules ever injected into man" and using it in vaccines is outlandish and criminal.So why does Washington sanction its use? According to Matsumoto: "scientists in the United States are now literally invested in squalene. Army scientists who developed the second generation anthrax vaccine have reputations to protect and licensing fees to reap (as well as) worldwide rights to develop and commercialize the new recombinant vaccine for anthrax" and ones for other health threats.
Disturbingly, "Many of the cutting-edge vaccines currently in development by the NIH and its corporate partners contain squalene in one formulation or another. There is squalene in the prototype recombinant vaccines for HIV, malaria, herpes, influenza (including the swine strain), cytomegalovirus and human papillomavirus." Some of these "are intended for mass immunization(s) around the globe" and that possibility should terrify everyone enough to refuse any mandate or doctor's prescription to take them.Another problem is that "Autoimmunity (takes) years to diagnose" because early symptoms (headaches, joint pain, etc.) are so vague they can easily be from other causes.From inception, vaccines have always been dangerous enough for some experts to call them biological weapons undermining health, manipulating and crippling the immune system, and creating the possibility of future debilitating diseases.
So Big Pharma's solution is new, more potent genetically engineered vaccines and drugs that may end up harming or killing many who take them, especially people with weakened immune systems.Matsumoto and others sounded the alarm to alert everyone to avoid these poisons masquerading as protective drugs. In fact, they benefit only the bottom lines of companies that manufacture them and scientists reaping generous royalties.Stephen Lendman is a Research Associate of the Centre for Research on Globalization. He lives in Chicago and can be reached at firstname.lastname@example.org.