PR Newswire WASHINGTON, March 9, 2026 WASHINGTON, March 9, 2026 /PRNewswire/ -- Parent Project Muscular Dystrophy (PPMD), in partnership with the Foundation to Eradicate Duchenne (FED), today ...
The Speak Foundation launched the LGMD Centers of Excellence, a network of clinics dedicated to improving care for people ...
The organizations are betting they can develop a redosable genetic therapy for LMNA-related congenital muscular dystrophy that could be a cure.
The Speak Foundation today announced the launch of the LGMD Centers of Excellence, a national network of leading academic ...
The Indiana-based Muscular Dystrophy Family Foundation is now accepting applications for its annual educational scholarship, which supports Indiana residents living with muscular dystrophy and related ...
Karen Guillmeno’s son, Hunter, was diagnosed with Duchenne muscular dystrophy — a rare genetic disorder involving progressive muscle degeneration — in 2016. The condition primarily affects males in ...
Born with a rare form of muscular dystrophy, Peri Finkelstein has never let her disorder define her. Instead, the 24-year-old New Yorker has used her challenges as a springboard to make the world a ...
ST. LOUIS — After spending a lifetime accepting checks donated to the Muscular Dystrophy Association, KSDK anchor-reporter Mike Bush got to present that organization with a check. The TEGNA Foundation ...
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