Tesfa is an impressive young Australian living with Duchenne Muscular Dystrophy (DMD). In this video, Tesfa, his mum and his school community share the unique obstacles he navigates, his plans for a future in social work, and the positive influence he has had on his peers.HEAR MORE PERSONAL STORIES
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MDF is the national voice for Australia's neuromuscular community.
We facilitate collaboration between our state and territory members and lead national initiatives that make a significant difference to the neuromuscular community.
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