(ARTICLE BELOW)
Mr. Wormser,
We are talking about all the immune suppression outcomes
of the likes of OspA, about which you know and about which
you have published:
http://www.actionlyme.org/PresPam14.htm
You're ^^^ IN THERE, buckaroo.
We're not talking about INFLAMMATION as the
nature of a "stealth-pathogen," remember?
http://www.actionlyme.org/JohnDunn_Brookhaven.htm
You Lyme crooks are, but you know we are not.
What is the treatment for *tolerance* to mycoplasma in
the blood? What is the treatment for Paul Duray's
mutated lymphocytes? Your OspA-induced
disease-set (Greatest Imitators- OspA vaccination) is far
worse than persisting spirochetes. There isn't much anyone
can do once they're ruined by Chronic Lyme or Late Untreated
Lyme (ALS, MS, Cancer, mycoplasmal tolerance in the
RBCs, as discussed by Joe Tully...), or the diseases-set you
subject them to because *you* are lying about the case definition:
Here is *your* case definition:
http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=8308100
^^^You claim that the Lyme-ELISA followed by Western Blot
detects only 9/59 CONVALESCENT CASES (contrary to what
Shapiro implied, while lying on NPR), yet you support the
Klempner Kryme:
http://www.actionlyme.org/MKLEMPNER.htm
which is based on your 15% accuracy assessment
of the current CDC standard for a "case."
What do you have to say for yourself?
The dung-breathed crew of medical whores you
pimp for don't have the intellectual capacity to
report *your* *reports* to the new IDSA panel (or the
USDOJ or the CT AG), which is why they were picked
for your new IDSA panel: They're all either hoes or tards.
And far be it from a medical whore to not be a tard, since evil
and lazy is the nature of stupidity.
Why don't you just hang it up?
Seriously.
Kathleen M. Dickson
http://www.actionlyme.org
http://www.ncbi.nlm.nih.gov/pubmed/19597005?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum
Clin Microbiol Rev. 2009 Jul;22(3):387-95.Click here to read Links
Antibiotic treatment of animals infected with Borrelia
burgdorferi.
Wormser GP, Schwartz I.
Division of Infectious Diseases, Department of Medicine, York
Medical College, Munger Pavilion Room 245, Valhalla, NY 10595, USA.
gary_w...@nymc.edu
Despite resolution of the objective manifestations of Lyme disease
after antibiotic treatment, a minority of patients have fatigue,
musculoskeletal pain, and/or difficulties with concentration or short-
term memory of uncertain etiology; these are called post-Lyme disease
symptoms or, in more severe cases, post-Lyme disease syndrome or
"chronic Lyme disease." Several recent studies in which Borrelia
burgdorferi-infected animals were treated with antibiotic therapy have
demonstrated the presence of PCR positivity for B. burgdorferi DNA in
the absence of culture positivity. In mice that were treated with
antibiotic therapy, residual spirochetes could be taken up by ticks
during a blood meal and could be transmitted to SCID mice. These
spirochetes are attenuated; their presence is not associated with
either inflammation or disease. In this review the methodology and
findings of these studies are critically analyzed, and the
significance of the results with regard to human Lyme disease is
evaluated, with special emphasis on whether these studies provide
useful insights into post-Lyme disease syndrome. A serious
methodological concern is the failure to consider the pharmacokinetic-
pharmacodynamic properties of the antibiotic in choosing the dosage
regimen used. We conclude that there is no scientific evidence to
support the hypothesis that such spirochetes, should they exist in
humans, are the cause of post-Lyme disease syndrome.
"[Real] scientists are *fiercely* independent. That's the good
news."-- NIH's Top Fool, Anthony Fauci