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.
Gulf War Syndrome
Tuesday 20 January 2009
Something we’ve not mentioned on the website before is Gulf War Syndrome.
Although originating from the effects of military conflicts in the Middle East, many of Gulf War Syndrome’s symptoms are remarkably similar to ME/CFS.
To that end, we offer what we think is the most comprehensive overview of the disease. It comes from The Research Advisory Committee on Gulf War Veterans’ Illnesses:
The Research Advisory Committee on Gulf War Veterans’ Illnesses was created by Congress in 1998, and first appointed by Secretary of Veterans Affairs Anthony J. Principi in January, 2002. The mission of the Committee is to make recommendations to the Secretary of Veterans Affairs on government research relating to the health consequences of military service in the Southwest Asia theater of operations during the Persian Gulf War.
According to its charter, the guiding principle for the work of the Committee shall be the premise that the fundamental goal of Gulf War-related government research is to improve the health of ill Gulf War veterans. Research priorities will be judged against this standard.
[source: The Research Advisory Committee on Gulf War Veterans’ Illnesses website]
It’s a document that details all aspects of the disease and offers many recommendations:
It may take you a while to wade through – the document is 465 pages long – but it’s interesting and very pertinent to people with ME/CFS.
blog comments powered by Disqus