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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 !

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 lgmd awarness day
Diseases
29/09/2023

LGMD Awarness Day: Stronger Together!

The 30th of September is Limb-Girdle Muscular Dystrophy Awareness Day. At this occasion, the LGMD Interest Group of the AFM-Téléthon is planning an information day about these diseases in Evry. 

Visuel "Duchenne : breaking barriers"
Diseases
07/09/2023

World Duchenne Awareness Day: everyone mobilized !

The 10th World Duchenne Awareness Day, on September 7, is a call to action to break down the physical, social and healthcare barriers faced by the 250,000 people around the world affected by this disease. It's also an opportunity to take stock of advances in research into this disease, which is emblematic of our Association. 

Vignette - Europe
Diseases
05/09/2023

The history of myology in Europe

In an article published in July 2023, an Italian researcher traces the birth and development of myology. This medical science of muscle and its diseases has developed over time, not only thanks to the advent of tools and technologies that improve our knowledge of muscle, but also thanks to the international collaborations that have marked its history.

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!

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.