For Immediate Release
Natural Solutions Foundation
Motion for “Stop the Shot” Injunction Filed in DC District Court
Washington DC – October 15, 2009: The Washington civil and regulatory rights law firm of Swankin and Turner filed a Motion in the United States District Court for the District of Columbia today, petitioning the Court for an Injunction to stop the distribution of the “Swine Flu” 2009-H1N21-A Vaccines approved by FDA on September 15, 2009 by voiding the licenses granted to the drug companies to sell the vaccines. The US government has purchased the entire supply of the four vaccines approved by the government and a contract distributor is currently distributing the live-virus nasal mist version to 90,000 pre-approved sites throughout the country.
The Motion was filed in the case of Null, Laibow et al. v FDA [USDC 1:09-cv-01924], in which Natural Solutions Foundation is a named Plaintiff, the plaintiffs allege that the approvals of these uninsurable, un-safety tested vaccines was “arbitrary and capricious” — violating the FDA’s own rules and the laws governing the approval of drugs. The Complaint in the case was filed on October 9, 2009
The emergency Motion for Injunction states in part,
The Defendants’ decision to issue the aforesaid licenses, modified licenses or approvals is arbitrary, capricious and contrary to law, and there is a substantial likelihood that Plaintiffs will succeed on the merits of this action. Specifically, the approvals violate the Food, Drug and Cosmetics Act (FDCA) and other statutes cited in Plaintiffs’ Brief, the Defendant Agencies’ implementing regulations and the Administrative Procedures Act show the following. … There is significant scientific agreement among independent scientists that the foreseeable risk of a vaccine’s potential to cause harm cannot be determined without adequate testing and that this is especially true regarding the 2009-H1N1-A Virus which has been arbitrarily and capriciously declared to be in a state of pandemic emergency. Further, Defendants have published a plan on their web sites to adulterate the approved vaccines with an unapproved “oil in water” adjuvant (squalene, a squalene derivative, and/or a squalene/GP120 mixture along with other as yet undisclosed and unlabeled components).
The full eight page motion is at: http://drrimatruthreports.com/?page_id=3661
Among other relief, the order the plaintiffs are seeking provides:
…The issuance of an Emergency Use Authorization (EUA) referencing these inactivated-“novel A/H1N1”-influenza vaccines is stayed for Vaccines that permit the mixing of an adjuvant with a Vaccine outside of the Vaccine manufacturer’s Current-Good-Manufacturing-Practice-compliant facilities; and … Approval or use of these Vaccines be contingent upon clear restrictions mandating written fully informed consent and voluntary use, without coercion or risk of loss of liberty, right to health care choice, property, schooling, livelihood, licensure or other public good by any governmental entity.
Plaintiffs lawyers are seeking a hearing this coming week.
Here is the Health Freedom Action Item that tells your representatives and decision makers that you refuse to be a “Pharma Serf” and demand protection from forced vaccinations:
Ralph Fucetola JD
Natural Solutions Foundation
Trustee and Counsel