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ME/CFS Australia Ltd

 
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  ME/CFS AUSTRALIA (SA) INC

Registered Charity 698

Email:
sacfs@sacfs.asn.au

Mailing address:
PO Box 28,
Hindmarsh,
South Australia 5007

Office:
266 Port Road,
Hindmarsh,
South Australia 5007
Ph: 1300 128 339

Office Hours:
Wednesdays, 10am-3pm


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.

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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Vice-President’s Report
March 2001

1: Introduction
2: Who’s going to...?
3: Why a high turnover?
4: Independent teams
5: Issues to address
6: The way forward?
7: 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)

Vice-President’s Report (continued)

Conclusion

Do you believe ME/CFS is a terrible illness? It’s time for all who believe this to roll up their sleeves to have a go at making this society really work. This is the year of the volunteer and I reckon we deserve our fair share.

Maybe you can help, but if not – perhaps you have a friend or family member who can, or perhaps you belong to a community group where you could advertise for voluntary help.

There are many small jobs, and a number of big jobs. Even if you can only do a little, we need people to take on specific tasks and be prepared to stick at them. Remember that volunteering has its benefits – it gets you out of the house mixing with others, it provides opportunities to develop skills, and we can give anyone a reference who requires it.

Finally, it would be great to see as many of you as possible come along to our ‘Public Medical Lecture’ on International ME/CFS Awareness Day, May 12. It will be a great day, and it will be a chance for you to meet the new management committee.

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