Myalgic encephalopathy and chronic fatigue syndrome information for patients and medical professionals.
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.
Chronic fatigue syndrome information, support and advocacy resources, including a grassroots on-line action center.
Helps primarily people with chronic fatigue syndrome, who having no other recourse, would endure hunger, homelessness and/or medical deprivation.
An information, advocacy and support organization for CFS and Fibromyalgia Syndrome.
The NCF is a national non-profit that funds research and provides information, education, and support to people who have chronic fatigue syndrome, also known as CFIDS and M.E.
Promotes recognition of four related conditions: CFIDS/M.E. (chronic fatigue syndrome), fibromyalgia, Gulf war syndrome, and multiple chemical sensitivity.
An organization of people with CFS which supports, informs and helps patients to deal with this serious illness. An in depth look at this syndrome as well as frequently asked questions.
A Canadian organization dedicated to the study and treatment of M.E./CFS.
Providing support to patients in Connecticut with chronic fatigue immune dysfunction syndrome, CFIDS, chronic fatigue syndrome, CFS, fibromyalgia syndrome, FM.
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