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24 May 2012
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TUSKEGEE - By Jerry Leonard
1998, CIA Oilmen & Israelis plan to overthrow
Saddam for the oil.
Bush/Gore Oil/War-(Oct,2000)
Bush's own explainer (Oct
2000) re:
Iraq Oil
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To: dwhelan@forbes.com,
carol@drcarolgoodheart.com, lPickering@cdc.gov,
Durland.fish@yale.edu, Aag1@columbia.edu,
gary_wormser@nymc.edu,
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SpinLyme@yahoogroups.com, kshepard@calea.org,
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Cc: francam@ucia.gov, dr-ahmadinejad@president.ir,
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karla.dobinski@usdoj.gov,
christopher.christie@usdoj.gov,
richard.Levin@yale.edu, harold.koh@yale.edu,
james.phillips@yale.edu, inquire@aldf.com,
lyme@idsociety.org,
meganmcardle@theatlantic.com
Subject: "Time For Lyme" Idiots on Steve
Schutzer
Date: Mar 2, 2011 2:12 AM
ARTICLE BELOW
=-----------------------------
Steve Schutzer has known all about
the biomarkers for Lyme and that
CFIDS is a form of Lyme since the
1990s.
Schutzer is the author of this 1992
book:
http://www.actionlyme.org/Duray.htm
http://www.actionlyme.org/COLDSPRINGHARBOR.htm
http://www.actionlyme.org/FIBROLENNYCYTOKINO.htm
Fibro Lenny was talking about how
dysregulated cytokines are associated
with the sleep disorder associated with
Fibro-Femino.
And then if this symptom is related to
a real biomarker, then it is not Not
Enough Sexitis or Self-Poisoning:
http://www.actionlyme.org/MUNCHAUSENS.htm
In 2001, there was a Lyme.org conference
in Hartford where a panel of 4 experts
including
Schutzer discussed modifying the
diagnostic
standard for Lyme disease to make one
antigen
(band 23 or OspC the brain-invasion
antigen)
diagnostic.
Schutzer was on the panel.
http://www.lyme.org/01_agenda.html
He said such a proposal was no good
because
"a very high percentage of Chronic
Fatigue patients
have some antibodies against Lyme."
http://www.lyme.org/01_agenda.html
Steve Schutzer absolutely is NOT Lyme
or SICK-PEOPLE-FRIENDLY.
And we all already know about all the
Biomarkers of Illness:
http://www.actionlyme.org/BIOMARKERS2.htm
http://www.actionlyme.org/070430.htm
They were all identified by ^^^ the
crooks,
themselves, in the 1990s.
I am so sick of loud-mouth dopes trying
to run Lyme/CFIDS activism.
DO NOT hang with Steve Schutzer. He most
certainly knows that all that I have
been
telling you is true, even to include
a chapter in his 1992 book:
http://www.amazon.com/Lyme-Disease-Immunologic-Approaches-Communications/dp/0879693770
by Raymond Dattwyler and Ben Luft which
speaks about how the current testing for
Lyme is bogus.
And that Lyme should be diagnosed as
Relapsing Fever.
KMDickson
http://www.actionlyme.org
=================================
http://www.healthnewsdigest.com/news/Disease_420/New_Hope_for_Lyme_Disease_Patients.shtml
New Hope for Lyme Disease Patients
By Time for Lyme
Mar 1, 2011 - 10:36:51 AM
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(HealthNewsDigest.com) - March 1, 2011,
Greenwich, CT - Through "protein
profiling" of spinal fluid, a new
research study shows that healthy
individuals, certain Lyme disease
patients with persistent neurologic
symptoms, and chronic fatigue syndrome
patients possess different proteins in
their cerebrospinal fluid. This finding
provides evidence that chronic fatigue
syndrome and neurologic Lyme disease are
distinct disease entities.
“The potential for spinal fluid
biomarker detection to aid or actually
establish diagnosis of Lyme disease is
within our grasp,” according to Dr.
Harriet Kotsoris, Medical Director for
Time for Lyme, a Connecticut based
non-profit organization that has been
funding research for Lyme and
tick-borne diseases since 2002 and has
raised nearly $5 million to date.
The research was led by Dr. Steven E.
Schutzer of the University of Medicine
and Dentistry of New Jersey-New Jersey
Medical School, and Drs. Thomas
Angel, Tao Liu, and Richard D. Smith of
the Pacific Northwest National
Laboratory. The study, “Distinct
Cerebrospinal Fluid Proteomes
Differentiate
Post-Treatment Lyme Disease from Chronic
Fatigue Syndrome” is published in
the February 23rd issue of PLoS ONE.
Time for Lyme provided funds for the
study along with the National Institutes
of Health among other
organizations.
Dr. Kotsoris also notes that this study
exemplifies the key role
collaboration plays in research funding
among a wide variety of public and
private institutions.
Click here for more information on the
published study results:
http://www.timeforlyme.org/PDF/article_journal_pone_2_2011.pdf
About Time for Lyme: Time for Lyme’s
mission is to fund research for Lyme
and other tick-borne diseases and to
support these programs through
education, outreach and public policy
initiatives. For more information
call 203-969-1333 or visit
www.timeforlyme.org
Time for Lyme will hold a biannual
fundraising gala Illusions of Lyme at 6
p.m. on April 2 at the Hilton Stamford
Hotel in Stamford, CT. Proceeds from
the event will be used to support
research. For tickets or more
information,
call 646-502-9374.
Subscribe to our FREE Ezine and receive
current Health News, be eligible for
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HealthNewsDigest.com
For advertising/promotion, email:
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toll free: 877- 634-9180
KMDickson
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