DMD Voices
The latest insights and perspectives from people who have lived and struggled with DMD
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One in 50 million: How I was diagnosed with Duchenne muscular dystrophy
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When everything changed after a simple fall
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DMD doesn’t wait, and neither can families: A grandmother’s plea for better guidance
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The day hope for DMD knocked at my door, with a bill in hand
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Left in silence: Families facing rare diagnoses need better support
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What it was like to be diagnosed with Duchenne muscular dystrophy at 3 years old