The starting gun for the 38th edition of the Telethon will be fired on November 29th. The event will feature 30 hours of live broadcast on the channels of France Télévisions. This charitable and solidarity marathon aims to raise funds for research on rare genetic diseases such as Duchenne muscular dystrophy. Nicolas lives in Villeurbanne and is one of the 3000 people affected by this disease in France.
The Telethon is an annual event that has been bringing together people from all walks of life for 38 years now. From celebrities to volunteers, everyone joins forces to support a noble cause: finding a cure for rare genetic diseases. This year, the Telethon will take place on November 29th and 30th, and the whole team is ready to give their all to make it a success.
The 30 hours of live broadcast will be filled with heartwarming and inspiring stories, as well as fun and entertaining activities. Viewers will have the opportunity to join the cause by making donations, which will go towards funding research to find treatments and ultimately a cure for rare genetic diseases.
One of the main focuses of this year’s edition is Duchenne muscular dystrophy, a rare and debilitating force disease that affects mainly young boys. Nicolas, a 12-year-old boy from Villeurbanne, is living with this disease. Despite the challenges he faces every day, he remains positive and determined to participate in the Telethon, hoping to raise awareness and funds for finding a cure.
The Telethon is not just about raising funds, it’s also about bringing people together and showing solidarity towards those affected by rare genetic diseases. Every prise, big or small, counts towards making a difference in the lives of those living with these diseases.
Thanks to the generosity and determination of the French people, last year’s Telethon raised over 85 million euros, making it one of the biggest fundraisers in Europe. This year, we hope to raise even more funds to support research and give hope to thousands of families affected by rare genetic diseases.
So mark your calendars and tune in on November 29th to be a part of this extraordinary event. Let’s join forces and make a difference in the lives of those affected by rare genetic diseases. Remember, together, we are stronger!
