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 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.
Greetings to all our members and readers out there.
It is amazing how this condition is known world-wide, and presents itself identically, yet it is frustrating how little is done about it. We have to stick together and remain strong – the tide is in the process of turning for us.
We hope you find this edition of Talking Point interesting and informative; it has been a quiet quarter as far as our Society goes, but we have managed to find some interesting articles from other places. Thanks to Zoe Beveridge, and to Cherry and Katya Adams who have done some marvellous cartoon work and allowed us to publish it.
It is our desire to continue to improve Talking Point.
We really would love to have more original and local content so please send in you poems, recipes and letters. It’s great how people have already been supporting us.
We would like to take it further. Let us know which treatments are helping you – whether they be conventional or alternative. Talking Point is about the members of our Society helping each other.