ME/CFS AUSTRALIA (SA) INC
Registered Charity 698
PO Box 28,
South Australia 5007
Closed while relocating
1300 128 339
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.
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.
Aims of the Society
To improve the quality of life and health management of people with ME/Chronic Fatigue Syndrome, whilst supporting community education and research initiatives, which will lead to recognition by government health providers of the need for better outcomes in service provision.
People diagnosed with ME/CFS condition should be recognized as having a genuine illness and be entitled to equitable service provision. They should be entitled to fair treatment by medical and health professionals, as well as health and government service providers. They should not be discriminated against by health, medical, housing financial or educational bodies because of their diagnosis. One specific feature of ME/CFS as a condition – that it may fluctuate in severity – should be acknowledged.