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Since 1998, the FSHD Society has supported groundbreaking research on facioscapulohumeral muscular dystrophy (FSHD). Our grants have helped discover the genetic cause of FSHD, shown how it affects patients, and […]
Privacy The FSHD Society (FSHDS) respects the privacy of all visitors to our website. We will not sell, share or distribute your information (regardless of whether you provide it to […]
[…] month. Find out if there’s one near you: April 12, 2015 3:00 PM EST. An FSHD gathering in Hobe Sound, Florida Join host Mimi Brown and others living with FSHD […]
4q35 – A specific location on chromosome 4 where a genetic deletion linked to FSHD Type 1 occurs. The “q” refers to the long arm of the chromosome, and “35” […]
The FSHD Society is at the forefront of driving research, empowering families, expanding access to care, and advocating for lasting change. Your support fuels groundbreaking progress in treatments, provides life-changing […]
