ME/CFS South Australia Australia 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 South Australia Inc aims to keep members informed of various research projects, diets, medications, therapies, news items, 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.
About ME/CFS South Australia Inc
ME/CFS South Australia Inc. has been serving the ME/CFS community in South Australia since 1987, as a registered charity run by volunteers. We provide peer support, education and advocacy for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), Fibromyalgia, and related illnesses. ME/CFS SA does not receive any government funding but relies on memberships, donations, fundraising and volunteers to continue its work in the community.
That people with ME/CFS will:
Can We Make a Difference?
Despite the high prevalence of ME/CFS in the community (up to 240,000 Australians) and the life-changing impact of ME/CFS on both the individual and their families, there is a lack of recognition and understanding. ME/CFS SA is working hard on multiple fronts, at local, state, national and international level, to bring about change.
How can you help?
We would encourage all South Australians with a connection to this condition to join ME/CFS SA – together we can make a difference.
We support people with ME/CFS and their carers by:
We engage in advocacy efforts including, but not limited to: