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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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Disclaimer
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
Wednesday 22 July 2009
Phoenix Rising is an informative newsletter put out monthly by American CFS sufferer Cort Johnson on his Phoenix Rising website.
You can subscribe to the newsletter as well as download each issue.
The latest from Cort is a remarkable story of recovery.
Here’s Cort’s introduction:
This is undoubtedly the most unusual issue of Phoenix Rising that has been (or probably ever will be) published. It concerns the near complete recovery of someone I'd known and given up for dead. Besides the fact that his recovery was incredibly dramatic, it's also raises a lot of issues; not only is his Doctor outside his local area unknown, he also developed his own technique... is it possible that one unknown doctor working somewhere in America could have developed something this effective?
What to make of it? Did this person just happen to be the right patient for this technique? Or does this treatment constitute an enormous advance for ME/CFS patients? And if it does how in the world will it get out to them? Lots of knotty issues indeed.
In any case do read this story and feel free to ask any questions you have and post any comments at the new forum package on Phoenix Rising. If you're interested in trying to do the treatment feel free to e-mail me.
Check It Out at aboutmecfs.org/Story/MECFSRecovery.aspx .
Cort Johnson
Phoenix Rising – An ME/CFS Website at
http://aboutmecfs.org
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