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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 Suzanne Vernon
Tuesday 27 November 2007
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 offering from Phoenix Rising is an interview with Dr Suzanne Vernon (pictured), the new Scientific Director of the CFIDS Association of America:
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Phoenix Rising: Interview with the CAA’s New Scientific Director, Dr Suzanne Vernon (external link) |
Here is Cort’s introduction:
Phoenix Rising: Interview with the CAA’s New Scientific Director, Dr Suzanne Vernon
The CFIDS Association of America has embarked on a bold new course in the research arena.
A complete revamp of their program culminated in early November with the hiring of their first Scientific Director, Dr Suzanne Vernon. Dr Vernon was a pioneer in gene expression research and worked on the CDC’s CFS research team for over 10 years.
In this extensive interview she talks about her time at the CDC, about CFS research and her new job at the CFIDS Association of America.
You can find the interview at http://phoenix-cfs.org/IntVernon07.htm.
Following closely on the heels of this interview is Part I of a three-part interview with former CFSAC member, advocate, researcher and father, Dr Ken Friedberg. In Part I, Dr Friedberg takes us inside the CFSAC as they struggle with the government inattention and attempt to prod it into meaningful action.
Yours truly,
Cort
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