| 'Stop the Shot'
Litigation Filed Today in DC Court! http://salsa.democracyinaction.org/o/568/t/1128/p/dia/action/public/?action_KEY=1545 Read Press Release Here: http://www.healthfreedomusa.org/?p=3617 The Foundation's Court complaint alleges that the government failed to follow its own rules and applicable legislation in rushing the vaccine approvals in the absence of any of the requisite minimum scientifically sound and appropriate testing for both safety and effectiveness as required by law since 1964. Despite the FDA's intention to begin delivery this week of what they describe as the novel "Swine Flu" 2009-H1N1-A live virus nasal mist vaccine to 90,000 government-approved locations nationwide, six New Yorkers, including Natural Solutions Foundation's Medical Director, Rima E. Laibow, MD, and several NonGovernmental Organizations (NGOs) filed for an Emergency Injunction in the US District Court for the District of Columbia to prevent the distribution of what they believe are illegal, unnecessary and dangerous vaccines. The case of Null et al. v FDA et al. [Docket No. expected Friday, October 9, 2009] challenges the legality of the September 15th, 2009 licensing of four vaccines prior to any safety testing for what the government calls a "novel flu virus with pandemic potential." Although the government states that none of the vaccines contain adjuvants, that is manifestly untrue since the injected vaccines contain aluminum, a toxic adjuvant, and Novartis told the Natural Solutions Foundation on that same day that their approved vaccine contains MF59, their proprietary squalen adjuvant. The purpose of an adjuvant is to irritate the immune system into greater production of antibodies than it would otherwise create in response to a smaller antigen dose. Antigens are the most costly part of a vaccine to manufacture. Therefore, despite the enormous dangers, vaccine manufacturers are eager to use adjuvants. Adjuvants like squalene (also known as MF59, ASO 1, 2, 3 and 4) are highly toxic unapproved drugs in the US. The Novartis (approved) Swine Flu and GSK (awaiting approval) vaccines contain 1 million times more oil in water adjuvant (read, "squalene") than the devastatingly dangerous Vaccine A which caused the profound illness and death of so many previously healthy service men and women. Why so much squalene? Read on. A pair of patents filed in 1998 provide a means of turning the immune system of anyone receiving an injection of squalene at high doses plus a pig glycoprotein (very similar to the many biologically active human glycoproteins we all have) against the reproductive capacity of that person. That means that all of the children and pregnant women who are the first guinea pigs for these vaccines around the world could be rendered permanantly and irreversibly infertile through these shots. Perhaps this helps to explain the mystery of why the US government would invest almost half a billion dollars ($485M) to stock pile a dangerous, untested and unapproved injectable version of squalene. The rest of the mystery, of course, is solved when you recall that the FDA has said on its site that the squalene will be added to ("admixed") with the vaccines administered at the 90,000 sites to which they will be sent for injection. Natural Solutions Foundation <dr.laibow@gmail.com> |