Adjuvants to be added to H1N1 vaccine by Baxter and WHO programme body for “endless loop of self destruction”
On July 13th, WHO ordered the inclusion of oil-in-water adjuvants in the “swine flu” H1N1 vaccines to be distributed throughout the world this autumn on the recommendation of its vaccine advisory panel, packed with Baxter and pharmaceutical executives, in spite of the fact that clinical studies published by Baxter’s own scientific team that patented the H1N1 vaccine demonstrate that such adjuvants are, at best, useless.
“SAGE recommended that promoting production and use of vaccines such as those that are formulated with oil-in-water adjuvants and live attenuated influenza vaccines was important,” says the WHO pandemic briefing note.
In June 2008, Baxter’s Austrian-based scientists Ehrlich, Kistner and Barret published a clinical trial in the New England Journal of Medicine ((Previous Volume 358:2573-2584 June 12, 2008 Number 24) on the safety of an H5N1 whole-virus vaccine, in which they themselves go on record saying that the use of adjuvants did not improve the antibody response.
In spite of the evidence that adjuvants are at best useless, vaccine companies such as Baxter and Novartis are rolling out vaccines which contain adjuvants like squalene (MF 59), a substance added to the anthrax vaccine given to US soldiers, causing tens of thousands of Iraq Desert Storm soldiers to suffer permanent neurological damage.
Also, WHO is reported to have advised the use of “antigen sparing” protocols which means they are calling for the use of not much virus and lots of adjuvant.
The effects of adjuvants are so destructive to the human body that some people say that adjuvants are part of the next generation of biological or pharamlogical warfare.
“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 the 1930s that oil-based adjuvants are particularly dangerous, which is why their use has been restricted to experiments with animals,” reports the Idaho Observer.
“Keep in mind that the FDA determined that squalene was present in varying amounts in specific lots of anthrax vaccine administered to tens of thousands of Desert Storm personnel (without their informed consent). Not surprisingly, tens of thousands of Desert Storm veterans have suffered permanent neurological damage and exhibit symptoms commonly referred to as “Gulf War Illness.”
Extracts from the March 2005 Idaho Observer:
Squalene: The next wave of global pharmacological warfare
Fish oil vaccine adjuvant programs bodies for “endless loop of self-destruction”
by The Idaho Observer
It’s a race–will we all be injected with substances that program our own bodies to attack us before or after we realize that the newest weapon in the New World arsenal is our own immune system?
The theory that vaccines prevent the spread of infectious disease is based upon the belief that, by injecting a small amount of a disease into the body, it will develop “antibodies” that will prevent the injected person from contracting the disease against which he had been vaccinated.
The theory is complicated by the fact that attenuated doses of pathogens alone will not initiate an “antigenic response.” So, vaccines contain compounds known as “adjuvants” to intensify the body’s immune response.
Traditional adjuvants are alum (aluminum hydroxide), and thimerosal–which is 50 percent ethyl mercury and also serves as a vaccine “preservative.”
The neurotoxic affects of mercury are likewise not a secret and have been documented extensively in the scientific and medical literature since the mid-1800s.
Dr. Boyd Haley found that vaccines containing both aluminum and mercury greatly magnify the neurotoxic result of vaccination.
Most people understand that both aluminum and mercury are toxic. It is our body’s reaction to toxic exposure that vaccine advocates measure to determine vaccine efficacy. That elevated levels of mercury and aluminum can cause side-effects worse than the disease is not a consideration for most pro-vaccinators.
The new wave
West, who is director of the Vaccine Risk Awareness Network in Winlaw, BC, Canada, published the comprehensive, well-footnoted article “A Look into the Scary World of Vaccine Adjuvants.” The article explains that modern, synthetic or recombinant vaccines are “purer” and less toxic to the body than their live and dead virus predecessors and, therefore, require more potent adjuvants to illicit an immune response. “This has created a major need for improved and more powerful adjuvants for use in these vaccines,” the article, Vaccine Adjuvants: current state and future trends, published in the medical journal “Immunology and Cell Biology” stated.
Under this line of logic, alum is scheduled to be phased out and replaced with oil-based adjuvants such as squalene–an essential fatty acid derived from fish.
“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 the 1930s that oil-based adjuvants are particularly dangerous, which is why their use has been restricted to experiments with animals,” West wrote.
The following (in italics) is from West’s article. Keep in mind that the FDA determined that squalene was present in varying amounts in specific lots of anthrax vaccine administered to tens of thousands of Desert Storm personnel (without their informed consent). Not surprisingly, tens of thousands of Desert Storm veterans have suffered permanent neurological damage and exhibit symptoms commonly referred to as “Gulf War Illness.”
“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.
“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.”