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>From the New Paradigms Project [Not Necessarily Endorsed]:
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From: William Gazecki <[EMAIL PROTECTED]>
To: Carolyn Ford <[EMAIL PROTECTED]>; Derek Casari <[EMAIL PROTECTED]>; Deborah 
Dunston <[EMAIL PROTECTED]>; Kathleen Mulcahy <[EMAIL PROTECTED]>; Laura Abeyta 
<[EMAIL PROTECTED]>; Lloyd Miller <[EMAIL PROTECTED]>; Michael Tobias 
<[EMAIL PROTECTED]>; Nancy Miller <[EMAIL PROTECTED]>; Roger Aronoff 
<[EMAIL PROTECTED]>; Toni deMarco <[EMAIL PROTECTED]>
Subject: New `Tuskegee-Like Experiment' Planned
Date: Sunday, February 20, 2000 1:17 PM

Subj:   New `Tuskegee-Like Experiment' Planned with Pneumococcal...
Date:   2/18/00 6:40:11 PM Eastern Standard Time

New `Tuskegee-Like Experiment' Planned with Pneumococcal Pneumonia
Vaccine,
Reported by Classen Immunotherapies

BALTIMORE, Feb. 18 /PRNewswire/ -- The following was released today by
Classen Immunotherapies, Inc.:

   The FDA cleared yesterday a controversial new pneumococcal pneumonia
vaccine with questionable safety and a US government advisory panel is
planning to selectively target black children and Native American
children forimmunization.  This plan is being criticized for making
children of certain racial minorities "human guinea pigs".  It is
possible that 1% or more of the
children who receive the vaccine may develop insulin dependent diabetes
or another autoimmune disease from the vaccine.

This week the Center for Disease Control and Prevention's Advisory
Committee
on Immunization Practices recommended that children under 2 not receive
the new
pneumococcal vaccine but that black and Native American children age 2-5
be
selectively targeted for immunization.  This policy has come under
criticism
because the vaccine has never been properly tested for safety and the
FDA has
been told by an expert that the vaccine is expected to cause an epidemic
of
autoimmune disease.

The controversial vaccine is the conjugated 7-valent pneumococcal
vaccine
which is really a combination of 7 different vaccines, each to a
separate
strain of pneumococcal pneumonia bacteria.  The vaccine is similar in
structure to the already marketed hemophilus meningitis vaccine, a
vaccine
linked to large epidemics of insulin dependent diabetes.

Dr. J. Bart Classen, an immunologist at Classen Immunotherapies,
published
data in the British Medical Journal (BMJ 1999; 319:1133) supporting a
causal relationship between the hemophilus vaccine and the development
of insulin
dependent diabetes.  The vaccine has been incriminated in causing over
58
cases of insulin dependent diabetes per 100,000 children immunized in
Finland.  Dr. Classen told the FDA at a recent meeting that the 7 valent

pneumococcal vaccine may be 7 times as toxic as the hemophilus vaccine,
possibly causing an estimated 400 to 700 children to develop insulin
dependent diabetes/100,000 children immunized.  These cases of diabetes
may
not occur until 3.5 to 10 years following immunization.

"The government's plan to selectively target black and Native Americans
is
likely to have the effect of genocide, 0.5% of children who receive this

vaccine may develop insulin dependent diabetes from the vaccine and
diabetes is just one of many life threatening autoimmune disease,"
states Classen.
"I believe the vaccine clearly should not have been approved by the FDA
because it does not meet the criteria for approval based on US law."

Dr. Classen's research has been published in numerous journals and
featured
in national news reports. For the latest information on the effects of
vaccines on insulin dependent diabetes and other autoimmune diseases
visit
the Vaccine Safety Website (http://vaccines.net)

Classen Immunotherapies, Inc.
6517 Montrose Avenue
Baltimore, MD  21212  U.S.A.
Tel: 410-377-4549
Fax: 410-377-8526

--
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 Many answers are questionable."


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