Halperin vs Fallon's, the only long term treatment study

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Mort Zuckerman

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Apr 16, 2009, 6:35:55 AM4/16/09
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Subject: Halperin vs Fallom's, the only long term treatment study

Date: Apr 16, 2009 6:31 AM

Here Halperin neglects to mention that the
only long term treatment study of Neuroborreliosis
was Brian Fallon's, where the patients got something
like 14 weeks of intravenous cefriaxone. The Klempner
http://www.actionlyme.org/MKLEMPNER.htm
"study" was only 30 days or "the standard of care," making
the Klempner study a report on the failed or "not enough
intravenous ceftriaxone" "standard of care"):
FALLON:
http://www.actionlyme.org/FALLON_DANGEROUS_TERRORIST.htm

There is no other long term treatment study. There
is only Fallon's.

No other long term treatment controlled study has
ever been performed. Fallon study proved that
Lyme was a Relapsing Fever organism, which we
knew in 1981.

HALPERIN:
http://www.ncbi.nlm.nih.gov/pubmed/19367218?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum
Rev Neurol Dis. 2009 Winter;6(1):4-12.
Nervous system lyme disease: diagnosis and treatment.
Halperin JJ.

Department of Neurosciences, Atlantic Neuroscience Institute,
Summit, NJ.

Lyme disease, the multisystem infectious disease caused by the
tickborne spirochete Borrelia burgdorferi, frequently affects the
peripheral and central nervous systems. The earliest indication of
Lyme disease infection is usually erythema migrans. This large,
typically macular erythema, often with a target-like pattern of
concentric pale and red circles, gradually enlarges day by day,
potentially reaching many centimeters in diameter. In a significant
proportion of infected individuals, an acute disseminated phase leads
to seeding elsewhere in the body. Up to 5% of patients develop cardiac
involvement. In about 10% to 15% of patients, the nervous system
becomes symptomatically involved. Current serologic diagnostic tools
are quite useful, and standard treatment regimens are highly
effective. Oral antimicrobials have been shown to be effective in
European neuroborreliosis and presumably are equally potent in North
American patients. Long-term antibiotic treatment does not provide any
additional lasting improvement, but it is frequently associated with
significant morbidity.

----

Why do they, IDSA, persist in doing this?

Is it because the drugs induce the cyst form,
which is a replicating form? Do we end up with
even more spirochetes after treatment? Is that
the reason for IDSA's scientifically unsupported
"guidelines?"
http://www.actionlyme.org/Proposed%20Life%20Cycle%20for%20the%20Reiter%20Treponeme.htm

See Also:
http://www.actionlyme.org/RICOCHRON.htm
http://www.actionlyme.org/BIOWEAPONEERS_CORIXA_YALE_TLRS.htm
http://www.actionlyme.org/BIOMARKERS2.htm


We would like to know eventually what the *real*
science is. It has never before occurred in the
history of medical science, that such a "medical" group
fought so hard for the continued abuse of victims of
an illness.

The New York Times has never done a story about
the Lyme Crymes, because the story they HAD, was
not published, resulting in Holc Noble's quitting
the NYT with a good "quiet money" package.


The ONLY TIME a journalist tried to show IDSA
was lying was through the film Under Our Skin, whereupon,
after its Saturday April 26th 2008 showing in NYC, this
RICO cabal caved, because they were clearly caught lying on
video:
http://www.actionlyme.org/080430_RICO_CABAL_CAVES.htm


But no other common media publication or television
news company ever ran a story about *WHY* IDSA caved to
the CT AG Blumenthal lawsuit.


Kathleen M. Dickson
http://www.actionlyme.org

"[Real] scientists are *fiercely* independent. That's the good
news."-- NIH's Top Fool, Anthony Fauci
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