L'AFM-Téléthon rassemble des familles déterminées à vaincre la maladie et soutient la mise au point de thérapies innovantes pour les maladies rares.
The official website for the AFM-Téléthon, a French non-profit organization dedicated to funding research on neuromuscular diseases and supporting affected families. The site serves as a hub for information on the annual Téléthon event, research advancements, and ways to contribute or get involved.
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Detailed information about the annual Téléthon event, including dates, locations, and how to participate.
Latest news and advancements in neuromuscular disease research funded by the AFM-Téléthon.
Secure online platform for making donations to support research and family support programs.
Information on how to volunteer for the Téléthon event or other initiatives.
Resources and support services for families affected by neuromuscular diseases.
Access to educational content about neuromuscular diseases, research, and the importance of genetic research.
Option to subscribe to a newsletter for regular updates on the Téléthon, research progress, and more.
Links to the AFM-Téléthon's social media profiles for community engagement and updates.
Online registration for participating in the Téléthon event or related activities.
Stories from individuals and families who have benefited from the AFM-Téléthon's work.
To defeat neuromuscular diseases by funding innovative research and providing support to affected families.
A major fundraising event broadcasted on French television, featuring entertainment, testimonials, and live donation appeals.
Significant contributions to the understanding and treatment of neuromuscular diseases, including gene therapy advancements.
The AFM-Téléthon has mobilized millions of French citizens to contribute to its cause, making it one of the most successful fundraising initiatives in France.
Collaboration with international research institutions and organizations to accelerate progress in neuromuscular disease research.
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