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Scott Miller and Company Premieres "A CALL TO ARMS 2009 EDITION" at the Camelot Theaters in Palm Springs
Date:3/18/2009

e adjuvant, the American Recovery and Reinvestment Act of 2009 contains an additional $1 billion dollars, part of which is earmarked to develop a new anthrax vaccine formulation and replace the current vaccine inventory, since the aluminum hydroxide adjuvant can cause nerve cell death.

The fact that the time-limited immunity provided by the anthrax vaccine requires a start-up five injection series over 18-months, and then an annual booster shot, is considered to be proof that the anthrax vaccine will interfere with the human body's ability to maintain immune system cell lines: in particular, memory B-cells which create antibodies in bone marrow; memory T-cells which can quickly produce a massive macrophage response, when you are re-infected; and regulator T-cells, which prevent auto-immune diseases by destroying anti-nuclear antibodies.

US military reservists, who leave active service for over one-year, are required to complete the entire anthrax vaccine start-up sequence if they are recalled to active duty.

It is important to note that the anthrax vaccine has never been approved for the prevention of human inhalation anthrax disease. The FDA has approved the anthrax vaccine as "safe" for production and distribution in 2005 and 2008, but has not approved the anthrax vaccine as a prevention to inhalation anthrax disease. There is no proof that persons exposed to aerosolized anthrax spores will be better protected by the anthrax vaccine, than by the immediate diagnosis and treatment with the generic methacillin antibiotic, doxycycline.

When animals vaccinated with the anthrax vaccine were challenged by aerosolized anthrax, 75% of the test animals died. Surviving animals showed evidence of permanent lung, liver, and lymphatic injury on autopsy.

It is important to note that the multi-symptom

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