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La Société Française de la Mucoviscidose (French Cystic Fibrosis Society)

Created in 2004, the French Cystic Fibrosis Society (Société Française de la Mucoviscidose, SFM) is both the Federation of rare disease reference centers and a learned society: it groups the professionals involved in the disease for care (hospital and private practice), care support (notably genetic, biology, and microbiology laboratories) and research (fundamental, clinical, and translational). This is an organization for reflection, dialogue, and proposals concerning the organization of cystic fibrosis healthcare and research.

https://muco-cftr.fr/index.php/fr/la-filiere/la-societe-francaise-de-la-mucoviscidose

L’association Vaincre La Mucoviscidose (French Cystic Fibrosis Association)

Created in 1965 and recognized for its public utility in 1978, it is managed by an elected board of directors composed for the most part of parents and patients as well as physicians, researchers, and supporters, all volunteers. Professional employees implement the actions serving the four missions of the association: heal, provide care, live better, and raise awareness. 

www.vaincrelamuco.org  

The Network’s partners

The rare disease reference centers (CRMRs) and the cystic fibrosis resource and skills centers (CRCMs)

The Network includes one coordinating center, four constitutive centers, and 42 CRCMs.

Local professionals

Healthcare networks

Genetics laboratories

Lung transplantation centers

Research laboratories