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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.



Charity Direct

ME/CFS Australia (SA) Inc is a member of Charity Direct.



ourcommunity.com.auDonate online

Information and Support 2004 is an online appeal that aims to improve our Information and Support Line.

Read more…



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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Benefits of Membership

Emerge

You will receive four issues of Emerge per year, which will keep you up to date with the latest information about ME/CFS, ME/CFS research and coping with ME/CFS.

Access to fact sheets and other information about ME/CFS.

Access to Support Groups.

Discounts on entrance fees to Public Meetings.

Access to members-only meetings (held intermittently).

and soon to come:

Priority access to Members section on Web site.

Priority access to a self-management course.

By becoming a member of the Society you are not just helping yourself, but standing for the cause of ME/CFS. We would love for as many people to stand with us as possible. Until we are able to get funding from the state government from the Society, and a commitment to ME/CFS research from the Commonwealth government, we have a battle on our hands for recognition. Now is the time to really get behind the Society.

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