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Associazione Malati di CFS onlus
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
The Associazione Malati di CFS onlus (Association of Sufferers of CFS, non-profit) is a patient advocacy group for chronic fatigue syndrome founded in 2004 and located in Pavia, Italy.[1]
Aims[edit | edit source]
- to raise awareness of the existence and severity of CFS, among doctors, public institutions and citizens
- medical research, including a biobank of blood samples[2]
Funding[edit | edit source]
Notable people[edit | edit source]
Members of the Executive Council
- President: Roberta Beretta Ardino
- Vice President: Maria Pia Cavalet
- Secretary: Maria Mariani
- Counselor: Marina Gasparotto
- Counsellor: Catia Gennari
Scientific Committee
- Dr. Lorenzo Lorusso
- Dr. Enrica Hair
- Dr. Catherine Zilli
- Dr. Chiara Magatti
Notable studies[edit | edit source]
History[edit | edit source]
Online presence[edit | edit source]
- Website
- YouTube
