Subject: [Anthrax-no] Rep. Gilman's remarks with Anthrax Legislation
Date: Fri, 23 Jul 1999 01:46:42 EDT
From: TRempfer@aol.com
Reply-To: Anthrax-no@onelist.com
To: undisclosed-recipients:;
From: TRempfer@aol.com
Rep Gilman appeared during the hearing yesterday and made remarks. Very
encouraging he showed up since he wasn't even on the committee. Also, the
full text of his official remarks as he introduced the bill on Monday on the
floor of the House is here:
<A
HREF="http://thomas.loc.gov/cgi-bin/query/D?r106:1:./temp/~r106AVjTgA:e0:">~r1
06AVjTgA:e0: at thomas.loc.gov
</A> and the text is also below for posting, if desired:
CONGRESSIONAL RECORD
------------------------------------------------------------------------
HALTING THE ANTHRAX VACCINATION PROGRAM, H.R. 2548 -- HON. BENJAMIN A. GILMAN
(Extension of Remarks - July 19, 1999)
------------------------------------------------------------------------
HON. BENJAMIN A. GILMAN
in the House of Representatives
MONDAY, JULY 19, 1999
•Mr. GILMAN. Mr. Speaker, I rise today to introduce H.R. 2548 , a bill to
halt the implementation of the Department of Defenses' Anthrax Vaccination
Program. I urge my colleagues to join me in supporting this worthy
legislation.
•This legislation would halt the continued implementation of the force-wide
Anthrax Vaccination Program within the Department of Defense. As my
colleagues may know, this program was the result of a decision reached by the
Secretary of Defense early last year that mandatory vaccination of all
personnel in the U.S. Armed Forces was necessary.
•Concerns about the program began shortly after its implementation earlier
this year and have increased as the number of troops receiving the vaccine
has increased. These problems attracted the attention of the Government
Reform Subcommittee on National Security, which initiated a series of
hearings in March. To date, the subcommittee has had three hearings, with a
fourth scheduled for this week.
•The congressional hearings held in March, April, and June have raised a
number of concerns about the vaccination program including its purpose, its
value, the manner in which it is being carried out, and its effects on those
who serve in uniform. These concerns have been heightened by recent media
reports and information circulating among those affected by the vaccine.
Subsequently, my office, and those of many of my colleagues, has received an
increasing number of contacts from concerned constituents, both members of
the Armed Forces, as well as their distraught parents or relatives.
•The Secretary of Defense set out four specific conditions that had to be met
before the vaccination program could start: First, supplemental testing to
assure sterility, safety, potency, and purity of the vaccine stockpile;
second, implementation of a system for fully tracking anthrax immunizations;
third, approval of operational plans to administer the vaccine and
communications plans to inform military personnel; and fourth,
•review of medical aspects of the program by an independent expert.
•According to the hearing testimony before the subcommittee, none of these
conditions was satisfactorily addressed before the vaccine program was
implemented.
•The most prominent concern raised relates to the overall effectiveness of
the vaccine. The FDA approval cited by the Defense Department was for a
vaccine that was designed to protect workers in the woolen industry from
cutaneous contact with anthrax spores. Conversely, the primary anthrax threat
facing military personnel is not from cutaneous, but weaponized versions of
the bacteria, which are inhaled by their victims. There has been little or no
testing of the vaccine's effectiveness in humans against this form of
anthrax. Some testing has been done on animals with mixed results, the most
promising returns coming from laboratory monkeys. However, to assume a drug
that has achieved moderately successful results in primates will have a
similar response with humans is only the start of basic research, not a
definitive conclusion based on solid scientific evidence.
•Moreover, Mr. Speaker, there is no evidence from the Defense Department that
this vaccine would be effective against altered or multiple anthrax strains.
Given that the Soviet Union placed a high priority on the development of the
deliverable multiple anthrax strains, this is a legitimate concern. Analysis
of tissue samples from Russians killed in an accidental anthrax release from
a production facility in the 1970's have indicated infection from a
combination of individual strains.
•A second major concern relates to the overall safety of the vaccine. As with
any drug, there are concerns about harmful side effects. Since 1970, the
primary recipients of the vaccine have been several thousand mill workers and
mostly DOD researchers. This limited civilian usage of the drug has resulted
in limited evidence of adverse reactions. The one exception to this was the
inoculation of approximately 150,000 gulf war troops. However, the Defense
Department's poor recordkeeping after the gulf war has made gleaning any
useful information about the vaccine's effectiveness or harmful side effects
impossible. In fact, a Senate committee studying gulf war illness in the
103rd Congress did not rule out the use of the vaccine as a cause of gulf war
syndrome.
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