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Blog Post
Blog Post
2023: Year of the Volunteer
By
Donald S. Wood, Ph.D., President and CEO, Muscular Dystrophy Association
|
December 30, 2022
Blog Post
Celebrating Our 2022 Advocacy Accomplishments
By
Mark Fisher
|
December 23, 2022
Blog Post
MDA Honors the Life and Legacy of Victor Wright
By
Chris Anselmo
|
December 22, 2022
Blog Post
Quest for Success: Peter Saleh
By
Rebecca Hume
|
December 22, 2022
Blog Post
Perspectives on Gene Therapy Products for Neuromuscular Disease
By
Sujatha Gurunathan
|
December 19, 2022
Blog Post
Research Study Alert: Survey Examining Transfers of Care in the SMA Community
By
Sujatha Gurunathan
|
December 14, 2022
Blog Post
Clinical Trial Alert: Medical Device Feasibility Study for People with Paralysis
By
Sujatha Gurunathan
|
December 14, 2022
Blog Post
Clinical Trial Alert: Phase 2 Study of a New Tool for Muscle Assessment in People with Neuromuscular Disease
By
Sujatha Gurunathan
|
December 14, 2022
Blog Post
2022 Highlights – The Year of Independence
By
Donald S. Wood, Ph.D., President and CEO, Muscular Dystrophy Association
|
December 9, 2022
Blog Post
International Day of Persons with Disabilities: The State of Neuromuscular Disease Advocacy Around the World
By
Larry Luxner
|
December 1, 2022
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