About Us

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

Press Releases

Nov 12, 2020

The Muscular Dystrophy Association Elects Renowned Medical Researcher and Scientist Donald S. Wood, PhD as President and CEO
Nov 10, 2020

Muscular Dystrophy Association Announces Facebook Live @MDAorg on Giving Tuesday, December 1 at 3pm ET For A Year-In-Review of Research & Clinical Trials for the Neuromuscular Community
Oct 29, 2020

Leading ALS Organizations Endorse the Improved Accelerating Access to Critical Therapies (ACT) for ALS Act
Oct 29, 2020

Facebook Live @MDAorg for November’s National Caregivers Month Caregiving for the Neuromuscular Community Hosted by Sarah Stoney, MSW, LSW Featuring Prow Sarnsethsiri, Leticia and Douglas Tatum Thursday, November 12 at 3pm ET
Oct 28, 2020

Muscular Dystrophy Association Wins 2020 Constellation SuperNova Award

Recognized in Tech Optimization and Modernization Category for Impactful Digital Initiative
Oct 28, 2020

Muscular Dystrophy Association Launches MOVR Visualization and Reporting Platform to Improve Patient Care and Accelerate Drug Discovery

Partnership with DNAnexus will enable 37 MDA Care Centers to analyze data from the MOVR Data Hub to better understand disease progression and compare outcomes across therapeutic categories

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