Suneel Research Foundation
Our mission is to spread awareness about Duchenne Muscular Dystrophy (DMD), raise funds to support treatments and find a cure for DMD. Currently there are more than 20,000 children in the United States suffering from Duchenne Muscular Dystrophy, and more than 100,000 worldwide, with a statistically higher number of identified cases in Western New York than the national average. THE FOUNDATION RAISES MONEY TO FOSTER AND ADVANCE MEDICAL AND SCIENTIFIC RESEARCH TO FIND A CURE FOR DUCHENNE'S MUSCULAR DYSTROPHY. IN ADDITION, THE FOUNDATION SEEKS TO PREVENT AND ALLEVIATE SUFFERING & PROMOTE EDUCATION & AWARENESS OF DUCHENNE'S MUSCULAR DYSTROPHY.
Founded
2002
481
X (Twitter)
9
Address
Buffalo
Suneels Light | Duchenne Muscular Dystrophy Home About Us Projects News Events Duchenne MD Get Involved More suneel39s light a beacon of hope Funding research to develop treatments and a cure forDuchenne Muscular Dystrophyand improving the lives of those affected by the disease. DUCHENNE MUSCULAR DYSTROPHY Duchenne Muscular Dystrophy DMD is a rare genetic disorder characterized by progressive muscle degeneration and weakness resulting from mutations in the dystrophin protein. While the absence of dystrophin leads to muscle damage and weakness advances in research provide hope for effective treatments. Though predominantly affecting boys girls can also be carriers of the gene.
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Suneel Research Foundation
In just two days, you will experience an evening filled with great food, premium open bar, live blues music and a benefit auction with spectacular packages that are just in time for the holidays…that is, if you purchase your tickets ASAP at https://www. suneelslight. org/event-details/2019-night-for-hope.
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