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.
We welcome your contributions – tell us about your experiences with exercise and/or CBT. Has your doctor ever suggested CBT? If so, did you go ahead with the treatment and was it helpful for you?
Please try your hand at a paper critique or summarise (if more appropriate) a research article for an upcoming edition of Talking Point. You can visit the monthly Research Abstracts list to select a referenced paper for this purpose.
Information for ME/CFS physicians
Graded Exercise Therapy for ME... or You?
A critique of the Powell et al methodology
This article was written to accompany the March 2001 Talking Point article by Paul Leverenz and Farrah Tate. Whilst reading these comments, please refer to a copy of the following reference article:
Why have we focused so much attention on this one article? It is important that our members are aware of the current trend in psychiatric research, focussing on Cognitive Behaviour Therapy (frequently abbreviated simply as CBT). Persons with ME/CFS must demand that peer-reviewed and respected journals only publish studies based on sound scientific protocol. In the future, it should be our group objective to submit a response to any further papers like Powell et al paper as an incorporated body (the ME/CFS Society of SA).