Corporate Media Gets You Ready for Your Forced Exp

[vienna]

http://justgetthere.us/blog/archives...or-Safety.html

The media is reporting on the governments preparation for a massive vaccination campaign this fall for the hyped up H1N1 hybrid flu virus. Recently Katherine Sebelius, the Health and Human Services Secretary, granted legal immunity for vaccine manufacturers during the stage 6 pandemic declared by the WHO. Even more troubling than the new vaccines or antivirals themselves, is the Emergency Use Authorization (EUA) declared by the FDA, which enables the use of expired stockpiles of Tamiflu or Relenza, and non-compliance with label requirements. The EUA authority will also permit the FDA to allow the use of “unapproved or uncleared medical products” during an established emergency.

The new stock of vaccines the governments purchased, has been fast tracked for approval by the FDA. Health officials admit that the clinical tests are about dosage amounts, and not safety. So the new vaccines being approved for the fall campaign, have the potential to cause severe harm or death, due to the lack of safety tests.

http://justgetthere.us/blog/exit.php...&entry_id=4612

The clinical trials are mainly aimed at calibrating the doses to give to patients, not to test if it is safe or not, officials stressed.

“We are not trying to find some yet unrecognized problem with the vaccine,” said Michael Osterholm, director of the Center for Infectious Disease Research and Policy at the University of Minnesota

This is an appalling statement considering the 1976 mass vaccination campaign for swine flu, that injured hundreds of thousands and resulted in dozens of deaths from Guillain-Barré Syndrome. It is also a very cryptic statement, unrecognized problems, meaning that they will not explore how the body will react to new vaccines with unapproved adjuvants like Squalene.

http://anthraxvaccine.blogspot.com/2...adjuvants.html

Meryl Nass, M.D., an authority on the anthrax vaccine, stated on her blog:
“A novel feature of the two H1N1 vaccines being developed by companies Novartis and GlaxoSmithKline is the addition of squalene-containing adjuvants to boost immunogenicity and dramatically reduce the amount of viral antigen needed. This translates to much faster production of desired vaccine quantities.”
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http://blogs.mercola.com/sites/vital...t-Exposed.aspx

Dr. Mercola explains the effects of squalene injected into humans in this excerpt from his article on the subject:



The difference between “good” and “bad” squalene is the route by which it enters your body. Injection is an abnormal route of entry which incites your immune system to attack all the squalene in your body, not just the vaccine adjuvant.

Your immune system will attempt to destroy the molecule wherever it finds it, including in places where it occurs naturally, and where it is vital to the health of your nervous system.[viii]

Gulf War veterans with Gulf War Syndrome (GWS) received anthrax vaccines which contained squalene.[ix] MF59 (the Novartis squalene adjuvant) was an unapproved ingredient in experimental anthrax vaccines and has since been linked to the devastating autoimmune diseases suffered by countless Gulf War vets.[x]

The Department of Defense made every attempt to deny that squalene was indeed an added contaminant in the anthrax vaccine administered to Persian Gulf war military personnel – deployed and non-deployed – as well as participants in the more recent Anthrax Vaccine Immunization Program (AVIP).

However, the FDA discovered the presence of squalene in certain lots of AVIP product. A test was developed to detect anti-squalene antibodies in GWS patients, and a clear link was established between the contaminated product and all the GWS sufferers who had been injected with the vaccine containing squalene.

The WHO even admitted the swine flu vaccine being fast tracked in the EU may be unsafe because it allows firms to bypass large-scale human trials.http://blogs.mercola.com/sites/vital...t-Exposed.aspx