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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: first Advocacy Edition

Thursday 7 July 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 latest issue of Phoenix Rising is Cort’s first Advocacy Edition, and it includes a very good feature on leading US clinician Nancy Klimas:

PDF

Phoenix Rising: March/April 2007 Special Edition – Advocacy Edition (PDF, 327KB)

Here is Cort Johnson’s introduction to the issue:

Welcome to the first Advocacy Issue of Phoenix Rising.

This issue includes a report from Lobby Day and the CFSAC Meeting, it takes a look at the accomplishments we have achieved over five or six years and provides the conclusion of a series of papers on the major effort of the past five years by the NIH on CFS: the Neuroimmune Grant Package. In this last part we assess the how the NIH did and what conclusions we can draw from this effort.

Next up we’ll focus on the startling new CDC prevalence paper thats making big waves in the CFS community.

You can access the newsletter at the below URL or by opening the PDF.

http://phoenix-cfs.org/PR II SP Ed. Lobby Day RFA.htm

http://phoenix-cfs.org/PR II V VI Mrch 20April.htm

Happy reading,

Cort.

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