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Healthcare

Blog Post

MDA National Ambassador Blog- Embracing the Power of Giving and Gratitude: Ira’s Journey with MDA

By MDA Staff | November 10, 2023
Blog Post

AGAMREE ® (Vamorolone), Now FDA-Approved, Offers Hope for Children Living with Duchenne Muscular Dystrophy

By MDA Staff | October 26, 2023
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Blog Post

In Case You Missed It…

By MDA Staff | October 6, 2023
A family poses with Disney's Pluto
Blog Post

Insurance Denials for Gene Therapy Treatment Delay Access to Care

By Rebecca Hume | September 29, 2023
Blog Post

Clinical Trial Alert: Phase 3 Study of Batoclimab in Adults with MG

By Sujatha Gurunathan | September 29, 2023
Young disabled man in wheelchair doing strength exercises for hands in the rehabilitation clinic. Doctor physiotherapist helping him
Blog Post

Simply Stated: Research Updates in Periodic Paralysis

By Sujatha Gurunathan | September 25, 2023
Blog Post

Research Study Alert: Observational Study of Cardiovascular Function in Children with BMD or DMD

By Sujatha Gurunathan | September 22, 2023
Blog Post

New Therapy Brings Hope for Late-Onset Pompe Disease

By Melissa Donahue | September 21, 2023
A doctor wearing a mask sits at the front of a room and addresses a group of women and children.
Blog Post

What Do Genetic Counselors Do?

By Jason Henninger | September 13, 2023
Young smiling manager with cup of tea looking at you while sitting by office window
Blog Post

Can Women and Girls Have Duchenne Muscular Dystrophy?

By Larry Luxner | September 7, 2023
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Muscular Dystrophy Association, Inc.
1016 W Jackson Blvd #1073
Chicago, IL 60607
800-572-1717 | ResourceCenter@mdausa.org

 

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The Muscular Dystrophy Association (MDA) is a qualified 501(c)(3) tax-exempt organization. ©2022, Muscular Dystrophy Association Inc. All rights reserved.

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