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Sarepta Talks Progress, Plans for DMD Gene Therapy Trials for SRP-9001
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Duchenne 'Tongue-on-a-Chip' Model Shows Muscle Stem Cell Weakness
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My Son Is Trying Something New, Tha…
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Living with Duchenne muscular dystrophy and our bundle of Joy

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Caring for someone with Duchenne MD: What care…
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Finding Accessible and Companion Seating With Multiple Wheelchairs Is Tri…
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Making Mobility Devices More Appe…
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Patricia Inacio, PhD - Science Writer | Muscular Dystrophy …
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Virtual Events Mark MDA's Muscular Dystrophy Awaren…

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Confronting the past as my oldest son takes senior-yea…
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DMD Patients with Respiratory Decline Gain Access to Raxone in US
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Traditional Chinese Medicine Used to Help DMD Patients in Study
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How one family is navigating Duchenne muscular dystrophy | Muscular Dystrophy News

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Daily life with a Duchenne muscular dystrophy survivor | Muscular Dystrophy News
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It’s Year 15 for Jared Sweet Golf Outing DM…
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Living with Duchenne musc…
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I'm glad my sons with DMD are not trick-or-treating this year
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My Son Is Bigger Than His Duche…

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How one family is navigating Duc…
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New Advances in Santhera’s Therapeutic Drug Development for Duchenne Muscula…
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FSHD Therapy ACE-083 Phase 2 Trial Doses First Patient, Acceleron Anno…
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An emergency preparedness plan is crucial for those with disabilities

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MD and Your Heart Monitor: 6 Things I …
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Sarepta's Gene Therapy for DMD Showing to Safety, …
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I welcome Agamree (vamorolone) approval with renewed optimism
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30 Days of MD: My Typical Teen's Journey With Duchenne

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Teaching students about life with limb-girdle muscular dystrophy
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Rare Disease Groups Welcome FDA's Embrace of Alternatives i…
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I wish all of my sons could have played football
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Report Highlights Innovative And Diverse Pipeline Of Products Fo…

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Teaching students about life with limb-girdle muscular dystrophy
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Abdominal Muscles Involv…
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Integrin Protein a Potential Muscular …
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Ongoing Clinical Trial Testing New Metho…
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PPMD 2024: Experimental DMD gene, muscle cell therapies poised for trials

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