Associazione Malati di CFS onlus

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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

Notable studies[edit | edit source]

History[edit | edit source]

Online presence[edit | edit source]

References[edit | edit source]

  1. ↑ Website - Welcome Letter
  2. ↑ Website - Work with

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