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L'AFM-Téléthon rassemble des familles déterminées à vaincre la maladie et soutient la mise au point de thérapies innovantes pour les maladies rares.
Our goal is to find a cure for Duchenne muscular dystrophy. With organized fundraising events and support from you, we can continue our mission and turn the dream of finding a cure into a reality.
MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.
Conquering Duchenne Muscular Dystrophy
Save Our Sons is the peak body for Duchenne muscular dystrophy in Australia. We have focused our energy and fundraising efforts toward finding a cure. Open Monday To Friday. Donate Online. Founded In 2008. Highlights: Founded In 2008, Donation Option Available.
The mission of Grampy's Charities is to raise funds and support for children's organizations. It is our hope that by partnering with comfort and research based charities we will be able to make a difference in the lives of kids who need us most.
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Comment savoir si votre enfant est atteint de dystrophie musculaire de Duchenne? Quels sont les symptômes? Voici ce que vous devez savoir.
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We are focused on the development of precision genetic medicines to treat rare neuromuscular and central nervous system diseases. Learn more about Sarepta.
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We raise funds for medical research to end Duchenne (DMD) by pushing ourselves on a meaningful trek through the Himalayan Mountains in Nepal.
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