Founded in 2001, the national association Fibromyalgie France is a non-profit organisation authorized by the Ministry of Health and Solidarity in 2007. It is headquartered in Paris and addresses patients and their families/friends all over the Country.
The association aims to support all kind of activities in the field of research, mutual support, information and promotion. Furthermore, it represents the interests of its members when dealing with public authorities and national media. It helps to distribute medical information as well as social and institutional news which are interesting for people suffering from fibromyalgia and related syndromes and/or chronic pain. Experience gained in recent times is taken as a basis for future action and reflection.