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Parent Project Muscular Dystrophy Overview Video

PPMD is leading the Duchenne Muscular Dystrophy community through its commitment to research, education, advocacy and compassion

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FSH Muscular Dystrophy Documentary
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FSH Muscular Dystrophy Documentary

Kids Meet a Guy with Muscular Dystrophy | Cut
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Kids Meet a Guy with Muscular Dystrophy | Cut

Gene Therapy for Duchenne: Translating clinical guidance into meaningful patient understanding
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Gene Therapy for Duchenne: Translating clinical guidance into meaningful patient understanding

ADHD Child vs. Non-ADHD Child Interview
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ADHD Child vs. Non-ADHD Child Interview

Doctor reveals undisclosed risks of COVID-19 vaccine
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Doctor reveals undisclosed risks of COVID-19 vaccine

Brendan's Hope - Muscular Dystrophy Association and Nemours Children's Hospital
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Brendan's Hope - Muscular Dystrophy Association and Nemours Children's Hospital

BrainPOP animation about Duchenne Muscular Dystrophy
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BrainPOP animation about Duchenne Muscular Dystrophy

How gaming helps Seth with his Duchenne Muscular Dystrophy
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How gaming helps Seth with his Duchenne Muscular Dystrophy

Living with Muscular Dystrophy
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Living with Muscular Dystrophy

Living A Full Life With Muscular Dystrophy
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Living A Full Life With Muscular Dystrophy

Webinar: Capricor Therapeutics — HOPE-3 Community Update
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Webinar: Capricor Therapeutics — HOPE-3 Community Update

SHRS Snapshots: Duchenne Muscular Dystrophy
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SHRS Snapshots: Duchenne Muscular Dystrophy

Campaign for new Duchenne Muscular Dystrophy drug to be approved | STV News report 14-03-25
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Campaign for new Duchenne Muscular Dystrophy drug to be approved | STV News report 14-03-25

Congenital muscular dystrophy
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Congenital muscular dystrophy

Neuromuscular Care and Genetic Considerations in Becker
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Neuromuscular Care and Genetic Considerations in Becker

Duchenne Muscular Dystrophy and Dystrophin
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Duchenne Muscular Dystrophy and Dystrophin

My Body Was Folded In Half When I Was Born | BORN DIFFERENT
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My Body Was Folded In Half When I Was Born | BORN DIFFERENT

Webinar: Exercise and Dystrophinopathy - What Families Need to Know
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Webinar: Exercise and Dystrophinopathy - What Families Need to Know

Emma Weatherley - FSHD Research & Clinical Trial Updates | MDQ Neuromuscular Seminar
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Emma Weatherley - FSHD Research & Clinical Trial Updates | MDQ Neuromuscular Seminar

Duchenne Muscular Dystrophy: Ryan's Story
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Duchenne Muscular Dystrophy: Ryan's Story

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