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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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President’s Report
AGM November 8, 2003
1: Introduction
2: Management Committee
3: Achievements
4: Grants
5: Finances
6: Key directions and issues
7: Thanks
8: Conclusion
Reports
President’s report (AGM Nov
8, 2003)
Management Committee report (Jan 2003)
President’s end of year reports (2002)
President’s report (Mar 2002)
President’s report (Jan 2002)
President’s report (Nov 2001)
Nat. Assn. President’s report
(Nov 2001)
President’s report (Sep 2001)
Miscellaneous reports (Jun
2001)
Vice-president’s report (Jun
2001)
Vice-president’s report (Mar
2001)
President’s Report (continued)
Conclusion
There are many people in this State who are affected directly or indirectly by ME/CFS. Their needs are paramount and the Society exists only so that their lives might be made more pleasant and productive. They deserve more support than the Society, alone and unaided, can give them. It makes all those of us who work for them more than a little angry that the Society has to operate without any level of State or Federal government support whilst societies serving similar or even smaller numbers of clients receive recurrent funding support. We won’t see that change in the near future. But we will persist in working towards it. In this and other ways the Society remains the best hope of a better deal for South Australians coping with the challenge of ME/CFS.
Peter Cahalan
November 8, 2003.
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