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From PRWeb
The FSH Society, the Massachusetts-based charity that has transformed the science of the little-known and incurable disease, facioscapulohumeral muscular dystrophy (FSHD), will be the beneficiary of a collection of fundraising events this fall. From Boston to Los Angeles, each event has the same mission – to raise awareness of the FSH Society and further FSHD research.
The list of 2015 fall events include:
“I am amazed and excited to see such unique events supporting the FSH Society this fall. We are so fortunate to have incredible volunteers dedicate their time and energy to planning these entertaining events,” said Daniel Perez, founder and CEO of the FSH Society. “The funds raised from these events will help us support our research efforts for 2015.”
Please find more information on the 2015 fall events here.
Affecting an estimated 870,000 people worldwide, FSHD is one of the most common muscle dystrophies. The genetic disorder presents a lifelong progressive loss of skeletal muscles, typically attacking the muscles of the face (facio), shoulder blades (scapula) and arms (humerus), though it may possibly progress to affect any skeletal muscle. Approximately one-quarter to one-third of patients end up in wheelchairs.