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
- 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
Notable people
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
History
Online presence
- Website
- YouTube
