ME/CFS AUSTRALIA (SA) INC Registered Charity 698 Mailing address: GPO Box 383, Adelaide, South Australia 5001 Office: 266 Port Road, Hindmarsh, South Australia 5007 Ph: (08) 8346 3237 ('834 MECFS') Office Hours: Wednesdays, 10am-3pm Support Line: (Mondays and Thursdays, 10am-3pm) Ph: (08) 8346 3237 SA country callers: Ph: 1300 128 339 (local call)
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.
Disclaimer 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. |
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The Trans-NIH Working Group on CFSSaturday 22 November 2008
Here’s their mission statement: The NIH is committed to supporting a coordinated, innovative and interdisciplinary biomedical CFS research program. We will continue to stimulate interest among researchers new to the area as well as to ensure that current researchers remain dedicated to submitting new and meritorious proposals. The coordination of NIH CFS research is now in the Office of Research on Women's Health (ORWH) of the Office of the Director (OD). We recognize CFS as a multisystemic illness that requires a thorough interdisciplinary approach encompassing the scientific missions of many of the NIH institutes and centers. The ORWH leadership role is exercised through the Trans NIH Working Group for Research on Chronic Fatigue Syndrome (WG), which it chairs and convenes monthly. The mission of the Trans-NIH Working Group for Research on Chronic Fatigue Syndrome is to: • Stimulate and support research on CFS within the context of the missions of all Institutes, Centers and Offices. This website endeavors to provide information on the CFSWG and its programs that is helpful to researchers, health care providers, people with CFS and their families, and the general public.
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