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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: Interview with Dr Ken Friedman Part II
Sunday 6 July 2008
Phoenix Rising is an informative newsletter put out monthly by American CFS suffererCort Johnsonon his website CFS Phoenix.
You can subscribe to the newsletter as well as download each issue.
The latest from Cort is Part II of an interview with Dr Ken Friedman.
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An Interview With Researcher, Advocate and Author Ken Friedman Ph.D. Part II (external link) |
Here is Cort’s introduction to the interview:
ME/CFS costs the US economy $25 billion dollars a year in economic losses and yet receives amongst the lowest amounts of research funding of any disease. Do you want to know why?
Check out Part II of Dr. Ken Friedman's three-part interview on ME/CFS In Part II this father of a FM/CFS patient, researcher, advocate, author and former federal advisory committee provides some blunt and at times rather surprising answers about how we got to this situation plus his view of the opportunities present.
You can access this interview at:
http://phoenix-cfs.org/InterviewFriedmanResearch.htm
Coming up right on the heels of this newsletter is a veritable barrage of information including the overview of the Congressional Briefing/CFSAC Meeting, an interview with our patient representative on the CFSAC Committee, Rebecca Artmann plus Dr. Baraniuk on spinal tapping his way to understanding ME/CFS (and my experiences as I get tapped), the overview of the scintillating Symposiun on Viruses on CFS, and the third part of Dr Friedman's interview on advocacy and the future.
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