About Us

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

Press Releases

May 20, 2020

Muscular Dystrophy Association announces virtual Patient Focused Drug Development Meeting for Pompe disease July 13, 2020

Attendees will be participating virtually, with live polling, to ensure a broad range of experiences are shared with FDA, biopharmaceutical companies and key stakeholders.
May 4, 2020

Drink One for Dane

Dutch Bros Coffee takes ‘Drink One for Dane’ digital to continue the fight against ALS
Apr 29, 2020

Muscular Dystrophy Association's COVID-19 Emergency Fund Launches Extensive Campaign in ALS Awareness Month to Raise Funds for the Most Vulnerable During the Pandemic
Apr 20, 2020

MDA Frontline COVID-19 Response: Facebook Live Q&A to Protect the ALS Community with Dr. Matthew B. Harms
Apr 2, 2020

Muscular Dystrophy Association Announces Formation of Strategic Medical Advisory Team of Experts in Neuromuscular Care and Research

Barry Byrne, MD, PhD, will serve as Chief Medical Advisor; John W. Day, MD, PhD and Matthew B. Harms, MD, to serve as Medical Consultants. Dr. Byrne to lead a Facebook Live Conversation on Thursday, April 2 about how people living with muscular dystrophy,
Mar 31, 2020

Muscular Dystrophy Association to Host MDA Frontline COVID-19 Response with Dr. Barry Byrne, a Facebook Live Q&A on Protecting Neuromuscular Disease Community in Midst of COVID-19 Pandemic

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