Limb Girdle Muscular Dystrophy (LGMD) is a rare and progressive genetic disorder with over 30 subtypes. LGMD can impact not only mobility but also the heart, lungs, and muscles that support breathing.
One subtype, LGMD2I/R9, is an FKRP-related form of the disease that affects an estimated 7,000 individuals in the United States and Europe. There is currently no cure or disease-modifying treatment for any type of LGMD, so care focuses on managing symptoms and maintaining function.
We’ll go beyond the diagnosis to explore life with FKRP-related LGMD and the remarkable community helping patients face the future with strength and hope.
