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DMD Voices

The latest insights and perspectives from people who have lived and struggled with DMD

  • Conor McAuley What Rare Disease Day means to me

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  • Conor McAuley Come fly with me! My journey to flying with Duchenne

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  • Sarka Palouckova Determination is taking us around the world for DMD care

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  • Sachin Munshi My world through eye gaze technology

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  • Sarka Palouckova William’s world: A grandmother’s journey through Duchenne

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  • Sachin Munshi DMD through my family, voice and eyes

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  • Steffni Randle One in 50 million: How I was diagnosed with Duchenne muscular dystrophy

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Rare Disease Companion (RDC) is a network of news and information websites that supports people living with rare diseases. Through accurate, authentic, and compassionate news coverage, feature-length articles, and patient-friendly educational material, RDC provides insights into living with rare diseases at every point along the patient journey.

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