Wednesday, July 8, 2009

Vaccine May Be More Dangerous Than Swine Flu

1. Vaccine May Be More Dangerous Than Swine Flu

http://w3.newsmax.com/blaylock/47a.cfm?s=al&promo_code=82E6-1


An outbreak of swine flu occurred in Mexico this spring that eventually affected 4,910 Mexican citizens and resulted in 85 deaths. By the time it spread to the United States, the virus caused only mild cases of flu-like illness.

Thanks to air travel and the failure of public health officials to control travel from Mexico, the virus spread worldwide. Despite predictions of massive numbers of deaths and the arrival of doomsday, the virus has remained a relatively mild disease, something we know happens each year with flu epidemics.

Worldwide, there have only been 311 deaths out of 70,893 cases of swine flu. In the United States, 27,717 cases have resulted in 127 deaths. Every death is a tragedy, but such a low death rate should not be the basis of a draconian government policy.

It is helpful to recall that the Centers for Disease Control with the collusion of the media, constantly tell us that 36,000 people die from the flu each year, a figure that has been shown to be a lie. In this case, we are talking about 300 plus deaths for the entire world.

This virus continues to be an enigma for virologists. In the April 30, 2009 issue of Nature, a virologist was quoted as saying,"Where the hell it got all these genes from we don't know." Extensive analysis of the virus found that it contained the original 1918 H1N1 flu virus, the avian flu virus (bird flu), and two new H3N2 virus genes from Eurasia. Debate continues over the possibility that swine flu is a genetically engineered virus.

Naturally, vaccine manufacturers have been in a competitive battle to produce the first vaccine. The main contenders have been Baxter Pharmaceuticals and Novartis Pharmaceuticals, the latter of which recently acquired the scandal-ridden Chiron vaccine company. Both of these companies have had agreements with the World Health Organization to produce a pandemic vaccine.

The Baxter vaccine, called Celvapan, has had fast track approval. It uses a new vero cell technology, which utilizes cultured cells from the African green monkey. This same animal tissue transmits a number of vaccine-contaminating viruses, including the HIV virus.

The Baxter company has been associated with two deadly scandals. The first event occurred in 2006 when hemophiliac components were contaminated with HIV virus and injected in tens of thousands of people, including thousands of children. Baxter continued to release the HIV contaminated vaccine even after the contamination was known.

The second event occurred recently when it was discovered that Baxter had released a seasonal flu vaccine containing the bird flu virus, which would have produced a real world pandemic, to 18 countries. Fortunately, astute lab workers in the Czech Republic discovered the deadly combination and blew the whistle before a worldwide disaster was unleashed.

Despite these two deadly events, WHO maintains an agreement with Baxter Pharmaceuticals to produce the world's pandemic vaccine.

Novartis, the second contender, also has an agreement with WHO for a pandemic vaccine. Novartis appears to have won the contract, since their vaccine is near completion. What is terrifying is that these pandemic vaccines contain ingredients, called immune adjuvants that a number of studies have shown cause devastating autoimmune disorders, including rheumatoid arthritis, multiple sclerosis and lupus.

Animal studies using this adjuvant have found them to be deadly. A study using 14 guinea pigs found that when they were injected with the special adjuvant, only one animal survived. A repeat of the study found the same deadly outcome.

So, what is this deadly ingredient? It is called squalene, a type of oil. The Chiron company, maker of the deadly anthrax vaccine, makes an adjuvant called MF-59 which contains two main ingredients of concern—squalene and gp120. A number of studies have shown that squalene can trigger all of the above-mentioned autoimmune diseases when injected.

The MF-59 adjuvant has been used in several vaccines. These vaccines, including tetanus and diphtheria, are the same vaccines frequently associated with adverse reactions.

I reviewed a number of studies on this adjuvant and found something quite interesting. Several studies done on human test subjects found MF-59 to be a very safe immune adjuvant. But when I checked to see who did these studies, I found—to no surprise—that they were done by the Novartis Pharmaceutical Company and Chiron Pharmaceutical Company, which have merged. They were all published in "prestigious" medical journals. Also, to no surprise, a great number of studies done by independent laboratories and research institutions all found a strong link between MF-59 and autoimmune diseases.

Squalene in vaccines has been strongly linked to the Gulf War Syndrome. On August 1991, Anthony Principi, Secretary of Veterans Affairs admitted that soldiers vaccinated with the anthrax vaccine from 1990 to 1991 had an increased risk of 200 percent in developing the deadly disease amyotrophic lateral sclerosis (ALS), also called Lou Gehrig's disease. The soldiers also suffered from a number of debilitating and life-shortening diseases, such as polyarteritis nodosa, multiple sclerosis (MS), lupus, transverse myelitis (a neurological disorder caused by inflammation of the spinal cord), endocarditis (inflammation of the heart's inner lining), optic neuritis with blindness and glomerulonephritis (a type of kidney disease).

The second ingredient, and one that greatly concerns me, is called gp120, a glycoprotein. Researchers found when it was mixed with squalene, the glycoprotein became strongly antigenic—that is, it produced a powerful and prolonged immune response to the vaccination. In fact, their studies show that with each dose, the intense immune reaction lasts over a year.

Now for the shocker—the glycoprotein-gp120, a major component of MF-59 vaccine adjuvant, is the same protein fragment isolated from the HIV virus that is responsible for the rapid dementia seen in AIDS patients.

Studies have shown that when gp120 is taken up by the microglia cells in the brain, it causes intense inflammation and makes the brain subject to excitotoxic damage—a process called immunoexcitotoxicity. This is also the cause of the MS and optic neuritis associated with vaccines that contain MF-59.

So, how would the gp120 get into the brain? Studies of other immune adjuvants using careful tracer techniques have shown that they routinely enter the brain following vaccination. What most people do not know, even the doctors who recommend the vaccines, is that most such studies by pharmaceutical companies observe the patients for only one to two weeks following vaccination—these types of reactions may take months or even years to manifest.

It is obvious that the vaccine manufacturers stand to make billions of dollars in profits from this WHO/government-promoted pandemic. Novartis, the maker of the new pandemic vaccine, recently announced that they would not give free vaccines to impoverished nations—everybody pays.

One must keep in mind that once the vaccine is injected, there is little you can do to protect yourself—at least by conventional medicine. It will mean a lifetime of crippling illness and early death.

There are much safer ways to protect oneself from this flu virus, such as higher doses of vitamin D3, selective immune enhancement using supplements, and a good diet.

3 comments:

  1. There is a report of a combination of MF59 and gp120 refer to phase I/II testing of an HIV/AIDS vaccine in a population of Thai volunteers in 2005. If the body creates antibodies to gp120, the antibodies (Immunoglobulin Alpha) could interfere with the HIV/AIDS virus' ability to penetrate helper-T cells. Glycoprotein 120 is the key "docking" mechanism for the retrovirus. See: http://www.pharmabiz.com/article/detnews.asp?articleid=30126

    gp120 has never been a component of the BioThrax human anthrax vaccine.

    The main ingredient for BioThrax is the "Anthrax Protective Antigen", a protein that binds to antibody sites and protects anthrax bacteria from attack by T-cells.

    MF59 Squalene - an organic oil - which is naturally occuring in human skin and fatty tissues, as well as in shark meat where it is harvested, was only detected in (6) batches of BioThrax produced in the mid-1990's, with the last reported batch to be FAV008. Gary Matsumoto's "VACCINE A" reports that these batches were prepared by PRI at the orders of Dr. Susan Welkos and Dr. Bruce Ivins to improve the efficiency of BioThrax to raise antibody concentrations against the Anthax Protective Antigen.

    MF59 Squalene is also believed to be a key component of OMER-2 anthrax vaccine tested on the Israeli Defense Forces beginning in 1998, a joint research project between the IDF and USAMRIID, which lead to the injury of over 1,500 IDF soldiers.

    MF59 Squalene binds to APA's domain 3 cell wall foothold, thereby unlocking APA's domain 1 structure so that FURIN can bind to APA. FURIN is a convertase protein - and is required to activate in place para-thyroid hormone, nerve growth hormone, von Willebrand factor, beta-secretase, gonaditropin, and transforming growth factor beta-1. MF59 in BioThrax improved the rate that FURIN would bind to APA, which increased the probability that antibodies (Immunoglobulin Gamma) would be created which will sequester FURIN, thereby leading to the emergence of auto-immune disease symptoms, such as rheumatoid arthritis, severe depression, chronic fatigue syndrome, ALS, muscular sclerosis, scleroderma, vasculitis, Sjogren's syndrome, thyroid cancer, skin cancer, and severe birth defects.

    MF59 Squalene has not been an active ingredient of BioThrax since the FAV008 batch released in the late 1990s.

    On the other hand, to reduce the chance of combining naturally occuring Squalene with the APA in BioThrax, since 2008, BioThrax has been released as an Intramuscular injection vaccine, and is no longer available as a Subcutaneous injection vaccine.

    It is still probable that exposure to APA without MF59 will result in FURIN sequestering Immunoglobulin Gamma. One in three injections will result in mild adverse reactions reported as muscle ache and mild tendonitis. Two in one thousand injections will result in severe life-threatening, even fatal, adverse reactions.

    BioThrax is not recommended by the FDA for children, women of child-bearing age, and the elderly. The FDA does not license BioThrax for the prevention of inhalation anthrax disease.

    BioThrax only provides temporary one-year tolerance to low-level anthrax exposure as may be expected working in normal agricultural settings. Annual booster shots are required, because BioThrax immunity impairs the ability to maintain memory B-cell, memory T-cell, and suppressor T-cell populations by reducing FURIN concentrations. Exposure to BioThrax can result in reduced immunity to disease.

    If inhalation anthrax disease is diagnosed, a simple course of low-cost doxycycline is recommended. Ciprofloxacin is not recommended because prolonged exposure can result in chronic tendonitis, ruptured tendons, and birth defects.

    For more information, ask your theater manager to screen Scott W. Miller's documentary "A CALL TO ARMS 2009 EDITION." See the YouTube channel here: http://www.youtube.com/scottmillerandco

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  2. If a severe immune reaction to BioThrax occurs, patients should immediately consult a board certified immunologist.

    Immune suppression therapy may be recommended. Such therapy may use synthetic steroids to suppress the immune system.

    If lymphoma occurs as a result of BioThrax exposure, then chemotherapy and radiation therapy, followed immediately by bone marrow stem cell transplant may be required to stop the progression of auto-immune diseases.

    Once systemic human tissue damage has occurred, it is very difficult to repair.

    Please support 2009's HR Bill 1478 - the Sgt. Carmelo Rodriguez Memorial Bill - which finally grants the right to sue the US government for medical malpractice for medical services received while a member of the military. In 1950, the US Supreme Court case Feres v. United States was decided to deny this right to military personnel. Sgt. Carmelo Rodriguez died from complications due to skin cancer after receiving the BioThrax vaccine, and after being misdiagnosed while on station in Iraq. Please write your congressmen to support HR Bill 1478.

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  3. I am very ill from several of the military vaccines. I am a civilian doctor. Can you contact me about some of this content?
    Doktari

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