

Limb-Girdle Muscular Dystrophy, type 2D/R3 (LGMD2D), is a severe muscle-wasting and progressive disease caused by mutations in the alpha-sarcoglycan gene.
The International LGMD2D Patient Registry is free to join and vital for research. It is the only database for all patients afflicted with LGMD2D/R3.
Your generous donation will help support awareness, advocacy, and research to find effective treatments or a cure for LGMD2D/R3.
We accept grants and donations from Fidelity Charitable, Schwab Charitable, Vanguard Charitable, and all major DAF sponsors.
Donate below or email info@lgmd2d.org for more information.

Sign up to stay up to date with updates and progress within the LGMD2D/R3 community.

There are currently no approved treatments or a cure for LGMD2D. The incredible warriors fighting this disease around the world need your support. Please consider making a donation—no dollar is too small, and every dollar goes directly toward raising LGMD2D/R3 awareness, advocating for families, and driving the development of life-changing treatments. Join us in this critical mission. Your support truly makes a difference.
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