Speak Foundation Brings LGMD Advocates Representing More Than 20 states to Capitol Hill, Honors Bipartisan Rare Disease Champions

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Patient-led organization urges Congress to strengthen LGMD research and help promising rare- disease science reach patients faster WASHINGTON, Sept. 16, 2026 /PRNewswire/ -- Advocates living with limb-girdle muscular dystrophy (LGMD) traveled from across the country to Washington this...