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The Duchenne Hungary Foundation was established in November 2002, with the aim of coordinating the therapy of children suffering from Duchenne Muscular Dystrophy (DMD), SMA and other muscular disorders. The Foundation is a non-profit organization having its own budget: it has been supported by private individuals and companies in addition to the grants received from charitable organizations and the funds raised through regularly organized charity events. We truly believe that we can provide enormous support to families affected by DMD in managing their difficult life. More …

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