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ME/CFS AUSTRALIA (SA) INC

Registered Charity 698

Mailing address:
GPO Box 383,
Adelaide,
South Australia 5001

Office:
266 Port Road,
Hindmarsh,
South Australia 5007
Ph: (08) 8346 3237
('834 MECFS')

Office Hours:
Wednesdays, 10am-3pm

Support Line:
(Mondays and Thursdays,
10am-3pm)
Ph: (08) 8346 3237

SA country callers:
Ph: 1300 128 339
(local call)


FIBROMYALGIA HELP:
Contact
Fibromyalgia SA
at the
Arthritis Foundation of SA
118 Richmond Road,
Marleston 5033
Ph: (08) 8379 5711

ME/CFS Australia (SA) Inc supports the needs of sufferers of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and related illnesses. We do this by providing services and information to members.

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Information and Support 2004 is an online appeal that aims to improve our Information and Support Line.

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ME/CFS Australia (SA) Inc aims to keep members informed of the various research projects, diets, medications, therapies etc. All communication, both verbal and written, is merely to disseminate information and not to make recommendations or directives.

Unless otherwise stated, the views expressed on this Web site are not necessarily the official views of the Society or its Committee and are not simply an endorsement of products or services.

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Phoenix Rising: January/February 2007 issue

Tuesday 10 April 2007

CFS Phoenix Phoenix Rising is an informative newsletter put out monthly by American CFS sufferer Cort Johnson on his website CFS Phoenix.

You can subscribe to the newsletter as well as download each issue.

The January/February 2007 issue has been published and is now available for download:

PDF

Phoenix Rising: January/February 2007 (PDF, 69KB)

Here is Cort Johnson’s introduction to the issue:

Welcome to the Jan/Feb Edition of Phoenix Rising.

In this edition we take a look at a complex but possibly very important mathematical model the CDC has developed in order to understand the problems with cortisol in CFS. This is the first time that I am aware of that anyone has gone to the trouble to develop a mathematical model involving a process found in CFS.  The CDC obviously thinks this is quite important.

We also look at a report from a different set of researchers that appears to verify the CDC’s model and the beginning of what should be a series of reports from the  second set of the very intriguing Seattle intensive twin studies. This series is starting off with a bang with evidence of reduced brain activity in CFS patients.

Be sure to check out Rich Von Konynenburg’s new additions to the website as well.

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