To support research and clinical trials to speed the development of treatments and a cure for LGMD2D.
Limb-Girdle Muscular Dystrophy, type 2D / R3 (LGMD2D), is caused by mutations in the alpha-sarcoglyan gene that lead to a deficiency of functional alpha-sarcoglycan protein.
LGMD2D causes weakness of muscles in the hip, shoulder, and abdomen.
The International LGMD2D Patient Registry is free to join and is currently the only database for all patients afflicted with LGMD2D.
Your generous donation will help support research to find effective treatments or a cure for LGMD2D/R3.
Sign up to stay up-to-date with updates and progress within the LGMD2D community.
We are launching an LGMD2D Foundation merchandise store in early 2024! All proceeds will go to research, awareness & advocacy!