American Myalgic Encephalomyelitis and Chronic Fatigue Syndrome Society
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The American Myalgic Encephalomyelitis and Chronic Fatigue Syndrome, better known as the American ME and CFS Society is a United States patient group for people with myalgic encephalomyelitis and chronic fatigue syndrome.
Aims[edit | edit source]
Services[edit | edit source]
Notable people[edit | edit source]
- Erica Verrillo, founder
Patrons[edit | edit source]
Medical advisors[edit | edit source]
Research/Notable studies[edit | edit source]
History[edit | edit source]
Funding[edit | edit source]
Interviews and articles[edit | edit source]
Online presence[edit | edit source]
- Facebook page
- YouTube channel
See also[edit | edit source]
Learn more[edit | edit source]
References[edit | edit source]
- ↑ "What We Do". American ME and CFS Society. Retrieved March 24, 2021.
myalgic encephalomyelitis (M.E.) - A disease often marked by neurological symptoms, but fatigue is sometimes a symptom as well. Some diagnostic criteria distinguish it from chronic fatigue syndrome, while other diagnostic criteria consider it to be a synonym for chronic fatigue syndrome. A defining characteristic of ME is post-exertional malaise (PEM), or post-exertional neuroimmune exhaustion (PENE), which is a notable exacerbation of symptoms brought on by small exertions. PEM can last for days or weeks. Symptoms can include cognitive impairments, muscle pain (myalgia), trouble remaining upright (orthostatic intolerance), sleep abnormalities, and gastro-intestinal impairments, among others. An estimated 25% of those suffering from ME are housebound or bedbound. The World Health Organization (WHO) classifies ME as a neurological disease.
The information provided at this site is not intended to diagnose or treat any illness.
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history.