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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
January 2002
1: Welcome
2: Fundraising effort
3: Adelaide Bank fund
4: International Conference
5: Elections
6: Fundraising
7: RACP CFS Guidelines
8: Badge Day
9: Office hours
10: 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)
International Conference – Sydney December 2001
I was personally privileged to attend the International ME/CFS Conference in Sydney in December 2001. The conference was outstanding – with a truly international mix of speakers presenting a wide range of material.
We can be very proud as Australians that we were involved in putting together a world-class event. For those of you who didn’t catch the September Talking Point – I’m happy to let you know that our Society contributed $4000 to the event.
Dr Rosamund Vallings has written an excellent summary of the event and that has been included in the medical section.
Christine Hunter and her team are truly an inspiration. If you have not done so already, please visit the Alison Hunter Memorial Foundation Website. It is the best resource for ME/CFS in Australia. Take a bit of time to read about the foundation and read about Alison Hunter. You’ll see where Christine’s drive and motivation comes from.
From my point of view it was great to network with the committee members of other states. I think this is timely as there was a big turnover on the National Exec. The bulk of the National Association board were at the conference and having now met each other it will help us to function as a team. (The National board only meet by phone hookup).
The only disappointment is that the conference made a loss for the AHMF.
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