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Find here all the latest news on AFM-Telethon and rare diseases.

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Le parrain Mika et les familles ambassadrices sur le plateau du Téléthon 2024
Telethon
31/03/2025

€96,553,593 – an outstanding result for Telethon 2024!

€ 96, 553, 593 : this is the final amount raised during the Telethon held on 29 and 30 November 2024. This result reflects an extraordinary outpouring of solidarity, driven by millions of donors, volunteers and partners who have stood by families in their fight for nearly 40 years. It is also the outcome of the outstanding commitment of our patron, Mika, and the many presenters and professionals from France Télévisions, who powerfully amplified the voices of families and researchers united in their determination to defeat the disease.

79,801,520 euros raised during the thirty hours of the 2024 Telethon
Telethon
03/12/2024

79,801,520 euros : the battle goes on !

Mika, patron of the 2024 Telethon, made a heartfelt appeal for public generosity at the end of the show. Speaking to viewers from 200 countries, he encouraged everyone to make a donation on telethon.fr

Mika, parrain du Téléthon 2024
Telethon
20/09/2024

Telethon 2024: Mika is the new patron !

Alongside the hosts of France Televisions and surrounded by numerous artists, Mika will use all his talent, sensitivity and energy to support families in their fight against rare diseases. Discover his message !

Hélène atteinte d'une myopathie FSH
Event
20/06/2024

World FSHD Day: Advancing Research

On June 20, World FSHD Day reminds us of the importance of raising awareness and supporting research into facioscapulohumeral muscular dystrophy. Committed to the fight against FSHD, the AFM-Téléthon is making available a series of publications to enlight the advances in research by it, but also by many other neuromuscular diseases. 

bénévole tenant des ballons
Telethon
17/05/2024

Telethon 2024: Join the Cause on November 29 and 30!

While it is customary for the heart of solidarity to beat for the Telethon on the first weekend in December, this year, exceptionally, the Telethon will be held on November 29 and 30, to make way for the ceremony to reopen the Cathedral of Notre-Dame de Paris.
 

Carte de voeux 2024 avec les 4 ambassadeurs du téléthon 2023
AFM-Telethon
02/01/2024

Happy new year!


The AFM-Téléthon sends you its best wishes for the New Year and hopes that 2024 will be full of scientific breakthroughs, small and large joys, and shared victories!

Plateau du téléthon 2023 avec 100 chercheurs
Telethon
19/12/2023

Telethon 2023 : €80,671,222: Thanks to you! 

The Telethon 2023 ended on a high of €80,671,222, which shows the confidence and exceptional mobilization of donors and volunteers for this year's event, rich in victories against disease and promises for all those waiting for the diagnosis and treatment that will change their lives. We must not give up. 

Logo myology 2024 Paris
Event
14/11/2023

Myology 2024 in Paris: registrations and call for abstract are open

The 8th edition of international congress dedicated to neuromuscular science, MYOLOGY 2024, will take place in Paris from 22 to 25 April 2024. Registration and call for abstract are now open : don't miss an opportunity to showcase your latest study to an international community of scientists and healthcare professionals. The deadline for abstract submission has been extended until November 30, 2023 - 11:59 pm.

Cure through innovation booklet
AFM-Telethon
17/07/2023

The new Cure through Innovation booklet is out!

Cure through Innovation is a booklet that sums up the main actions and missions of the AFM-Téléthon association, as well as the key figures for 2022. The July 2023 edition has just been published!

Une personne dans la foule
Event
02/06/2023

1st European Myasthenia Gravis Day: All united to raise awareness of this disease

Characterized by fatigue and muscle weakness that fluctuate over time, autoimmune myasthenia gravis is the subject of the very first European Myasthenia Gravis Day, on 2 June 2023. The aim is to give as many people as possible an understanding of the impact of this unpredictable and often invisible disease, and to standardize the way it is treated across Europe. 

Pr Judith Melki, présidente du conseil scientifique de l'afm-téléthon
AFM-Telethon
16/05/2023

A new president for the Scientific Advisory Board

On April 12, Prof. Judith Melki succeeded Odile Boespflug-Tanguy as president of the AFM-Telethon’s Scientific Advisory Board. Professor Emeritus of medical genetics, Judith Melki is at the origin of the discovery of the SMN gene, responsible for spinal muscular atrophy.

Jules and his parents walking for the Telethon
Telethon
03/04/2023

90,839,067 euros for the Telethon 2022: we have not given up. Thank you!

Thank you to everyone: donors, volunteers mobilized throughout France and abroad, families, partners, personalities! Thanks to your mobilization on December 2 and 3, the Telethon 2022 raised 90,839,067 euros! This tremendous result - the best since 2016 - shows how much the French people support the families’ fight against rare diseases.