About Us

Our mission is to empower people living with neuromuscular diseases to live longer, more independent lives.

Press Releases

Feb 26, 2024

Applications are Open for Muscular Dystrophy Association’s Inaugural College Scholarship Program to Elevate Higher Education Opportunities for Students with Neuromuscular Disease

MDA's Community Engagement programming includes additional resources and support for young adults.
Feb 22, 2024

Muscular Dystrophy Association Announces 2024 Muscle Walks in Local Communities Nationwide to Empower Families Living with Muscular Dystrophy, ALS, and Related Neuromuscular Diseases
Feb 15, 2024

Brooke Eby, ALS Patient and Advocate, to deliver Keynote Address at 2024 MDA Clinical & Scientific Conference

Following the keynote address, an expert panel discusses the challenges of neuromuscular disease in the age of therapies led by Sharon Hesterlee, PhD, Chief Research Officer, MDA.
Feb 1, 2024

Muscular Dystrophy Association Announces Seven Recipient Organizations of Advocacy Collaboration Grants

The Akari Foundation, All Wheels Up, Child Neurology Foundation, Cure CMD, Cure Rare Disease, Cure VCP Disease, and Christopher & Dana Reeve Foundation are recipients of MDA Advocacy Collaboration Grants.
Jan 31, 2024

Muscular Dystrophy Association Launches Rare Disease Day Campaign to Raise Awareness & Support for Neuromuscular Diseases throughout February

The rare disease community collaborates to raise awareness on Rare Disease Day, February 29.
Jan 30, 2024

Muscular Dystrophy Association Announces Recipient of 2024 MDA Legacy Award for Achievement in Research, is Jeffrey Chamberlain, Ph.D., Leading Professor in Gene Therapy

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