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1.
American Association for Chronic Fatigue Syndrome - AACFS
(site info)
Organization of research scientists, physicians, licensed medical healthcare professionals, and other individuals and institutions interested in promoting the stimulation, coordination, and exchange of ideas for CFS research and patient care.
http://www.aacfs.org/
2.
Action for M.E.
(site info)
Action for M.E. is a UK charity working to improve the lives of people with M.E. They campaign for more research, better services and treatments.
http://www.afme.org.uk
3.
Alison Hunter Memorial Foundation
(site info)
Myalgic encephalopathy and chronic fatigue syndrome information for patients and medical professionals.
http://www.ahmf.org/
4.
Waterloo Wellington Myalgic Encephalomyelitis Association
(site info)
A Canadian organization providing information about M.E., including coping strategies, diagnosing, the history, finding a physician and other related links.
http://ca.geocities.com/wwmea/
5.
American M.E. Society
(site info)
The Myalgic Encephalomyelitis Society of America concentrates on CFS research information and advocacy issues.
http://www.cfids-cab.org/MESA/
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