American Myalgic Encephalomyelitis and Chronic Fatigue Syndrome Society
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
 | This article is a stub. |
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.[1]
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]
- Website
- 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.
