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Blog Post
How the New LGMD Diagnostic Codes Could Benefit the LGMD Community
By
Paul Melmeyer
|
February 7, 2023
Blog Post
MDA’s 2023 Advocacy Plan
By
Mark Fisher
|
January 20, 2023
Blog Post
Celebrating Our 2022 Advocacy Accomplishments
By
Mark Fisher
|
December 23, 2022
Blog Post
2022 Highlights – The Year of Independence
By
Donald S. Wood, Ph.D., President and CEO, Muscular Dystrophy Association
|
December 9, 2022
Featured Article
When Will Air Travel for Passengers in Wheelchairs Get Better?
By
Shaila Wunderlich
|
November 18, 2022
Featured Article
MDA On the Road Launches at High-Impact Conferences to Advocate for Neuromuscular Community
By
MDA Staff
|
November 18, 2022
Blog Post
MDA Advocates Returned to Capitol Hill (Virtually)
By
Mark Fisher
|
October 25, 2022
Blog Post
The Latest on Newborn Screening
By
Mark Fisher
|
September 6, 2022
Blog Post
MDA Announces Advocacy Collaboration Grants Funding Opportunity
By
Mark Fisher
|
August 23, 2022
Blog Post
Top 5 Reasons to Attend MDA’s Virtual Summit & Hill Day
By
Mark Fisher
|
July 19, 2022
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