MDA
About Muscular Dystrophy Association
Muscular Dystrophy Association (MDA) is the #1 voluntary health organization in the United States for people living with muscular dystrophy, ALS, and related neuromuscular diseases. For over 70 years, MDA has led the way in accelerating research, advancing care, and advocating for the support of our families. MDA’s mission is to empower the people we serve to live longer, more independent lives.
To learn more visit mda.org and follow us on social media @MDAorg
People Behind MDA 75th Anniversary PSA: Ira Walker
How Are Registries Informing Neuromuscular Disease?
Updates in Research and Care: Vaccines and Neuromuscular Conditions Safety, Science, and Guidance
MDA Celebrates FDA Approval of First-Ever Treatment for TK2 Deficiency (TK2d)
MDA Webinar: Myositis
Spotlight On: Maintaining a Healthy Weight
Jose R Carlo Izquierdo, MD, FAAN, Co MDA Care Center Director, #MDAconference
Building Community, Finding Joy, and Redefining Resilience in CMT
Genetic Testing and Counseling for CMT What You Need to Know
Pain in CMT: Causes, Treatments, and Strategies
The ABCs of AFOs Orthotics and Bracing for CMT
Spotlight On CMT with the Hereditary Neuropathy Foundation
People Behind MDA 75th Anniversary PSA: Mindy Henderson
People Behind MDA 75th Anniversary PSA: Lily Sander
MDA Advocacy Institute: Supporting Medical Research Funding
Pain Management in SMA
Managing Respiratory Needs in SMA
Orthopedic Insights for Everyday Living
What’s Next in Gene Therapy
Life Takes Muscle: Striving for Independence in SMA