During four days, from 12 to 15th of September, researchers, clinicians and myology experts have attended the seventh International Congress of Myology, organized by AFM-Téléthon, in Nice, France. A good opportunity to exchange and share knowledge about myology and innovative therapies. Let’s have a look back at Myology 2022 with our researchers’ video interviews.
Welcome to AFM-Telethon new website !
Read more about AFM-Telethon’s social missions, main activities, and key figures in this new edition of Cure through Innovation.
It is a positive commitment, but France must set an example by perpetuating and amplifying a truly ambitious national policy.
First-ever United Nations resolution to increase visibility for persons living with a rare disease and their families
On 16 December 2021, the UN adopted the first-ever UN Resolution on “Addressing the Challenges of Persons Living with a Rare Disease and their Families.” A huge recognition for families with rare diseases.
Our fight to cure
60 years of fight against diseases
The French Muscular Dystrophy Association (AFM-Téléthon) is composed of patients and their families who are affected by genetic, rare and progressive diseases. Discover 60 years of fight.
Join the Telethon for french people abroad
You live abroad and want to be part of the great Telethon adventure? Join us!