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FSH Society Submits FY2014 Written Testimony U.S. House Appropriations Subcommittee on LHHSE for funding NIH and Research on FSHD at a level of $12 million annually More / Testimony in […]
FSHD patients and families are invited to attend the Stanford Hospital & Clinic’s Neuromuscular Program’s open house, taking place April 10, from 4:30 PM to 7:00 PM in the 2nd […]
Highlights include: Genetic Source of FSHD Type 2 pinpointed and outlined. FSHD patient climbs for hours through the mountains to visit gorillas in Uganda. FSH Society funds advances in understanding […]
Boston, MA / February 11, 2013 At the age of 28, Kevin Kirby was diagnosed with a disease that most people have never heard of. Called Facioscapulohumeral Muscular Dystrophy, or […]
The Centers for Disease Control Spotlights FSH Muscular Dystrophy
