The reason Lyme disease will never be taken seriously in today's media

Newsgroup Leader Katheen · medicine forum Guru Joined: 20 Jan 2006 Posts: 654

From: Kathleen Dickson <kmdickson0308@yahoo.com>
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Subject: The CDC and Scientific Fraud

Date: Wednesday, May 24, 2006 04:11:48 [View Source]

I don't bother with the United States any more, and
really neither does the rest of the world at this
point in history. The rest of the world knows we're
totally incompetent buffoons in all health and welfare
matters, not to mention the issues with Iran sitting
over 87 million geologic fault lines, Israel having
nukes and not complying with UN resolution 242 for
over 30 years, and the US dollar being worth squat.
http://actionlyme.org/SECURING_THE_REALM_BY_FRAUD.htm

Don't bother with any senators or congressmen or even
the media. They're *all* airheads. The new bourses
are going to nuke our economy no matter what. It's
too late for action. The successful fearmongering and
fraud got us all, but the rich peoples' money is in
the remainder of global resources. (Check our the
investments of the Bush-Walker-Weld banks and Yale's
Endowment fund or "The Yale Corporation.")

Kathleen
========From: "]
To: <SpinLyme@yahoogroups.com>
Subject: [SpinLyme] CDC = IDSA
Date: Wednesday, May 24, 2006 02:36:49

http://www.tic-nc.org/docs/Winter-Spring_TIC-NCNews2006.pdf

THE Centers for Disease Control WEB SITE CHANGES

The CDC has made some changes in the information on
tick-borne diseases. One principal difference is that
they have added a link to the 2000 Infectious
Disease Society of America's guidelines for treatment
of Lyme disease

(http://www.journals.uchicago.edu/CID/journal/issues/v31nS1/000342/000342.html

).

The CDC did not provide a link to the other standard
of care for Lyme disease, that from the International
Lyme and Associated Diseases Society Yr 2005 Lyme
disease
treatment guidelines
(http://www.ilads.org/burrascano_0905.html ) It might
be helpful to write the CDC and your congressional
representatives to ask why, if the CDC is going to
link to a private organization, that they do not
provide links to both standards of care for Lyme
disease since the issue is controversial and patients
have a right to know about both standards.

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Will Ketcher · medicine forum beginner Joined: 06 Mar 2006 Posts: 13

Why is it groups of survivors with serious illnesses, seem to have at
least one advocate who is totally unbalanced and disruptive to their
issue? I see it with Kathleen of the Lyme disease crowd. I see it
with Ilena Rosenthal of the breast implant people. I see it with Jan
Drew of the alternative medicine crowd.

Real survivors need real people to guide them --- not people who don't
have credibility and are a horrible nuisance.

With advocates like these --- why would anyone think their message has
merit?

It's frightening --- Surviors need real support and guidance.

eugeneshapiroisapig · medicine forum Guru Joined: 24 Mar 2005 Posts: 2108

it's not remarkable that there are individuals who espouse differing or
even radical views wrt any given situation. what is remarkable is that
there exist delusional cowardly twatlike sheeple such as yourself who
are obsessed with and frightened by them.

Nutcracker · medicine forum Guru Joined: 02 Mar 2006 Posts: 318

Spottdrossel wrote:

Google