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Read the latest news about issues affecting the neuromuscular disease community.
Blog Post
MDA Announces College Scholarship Program
By
MDA Staff
|
February 27, 2024
Blog Post
Inclusion Outshines Ableism on the Big Stage
By
Rebecca Hume
|
February 26, 2024
Blog Post
2023 in Review: A Letter from MDA President and CEO, Dr. Wood
By
Donald S. Wood, Ph.D., President and CEO, Muscular Dystrophy Association
|
December 11, 2023
Blog Post
In Case You Missed It…
By
MDA Staff
|
November 8, 2023
Blog Post
AGAMREE ® (Vamorolone), Now FDA-Approved, Offers Hope for Children Living with Duchenne Muscular Dystrophy
By
MDA Staff
|
October 26, 2023
Blog Post
Quest Media’s Inclusive Holiday Product Guide
By
Mindy Henderson
|
October 22, 2023
Blog Post
Insurance Denials for Gene Therapy Treatment Delay Access to Care
By
Rebecca Hume
|
September 29, 2023
Blog Post
MDA Continues to Lead the Way on Newborn Screening
By
Paul Melmeyer
|
September 1, 2023
Blog Post
MDA Announces New Round of Advocacy Collaboration Grants Funding
By
Mark Fisher
|
August 17, 2023
Blog Post
Quest Podcast: Accessible Air Travel and Advocacy Updates
By
MDA Staff
|
August 11, 2023
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