$15 for 15 Years of CureLGMD2i
CureLGMD2i is Celebrating 15 Years of Hope - Join us by supporting our $15 for 15 campaign!
15 years ago, CureLGMD2i, a 501(c)3 non-profit organization, was founded Keith & Kelly Brazzo when their daughter was diagnosed with Limb Girdle Muscular Dystrophy Type 2I/R9 (LGMD2I/R9). Their mission was to provide funding toward the development of a safe and effective treatment for LGMD2I/R9. Since that time, CureLGMD2i has supported over $1,350,000 in drug development, scientific conferences, awareness and advocacy programs for this ultra rare and progressive neuromuscular disease. We are getting closer to a cure, but we need your help to fund the next generation of gene editing therapies for LGMD2I/R9.
Celebrate with us by donating $15 (or more) to fund vital research and help move us closer to a cure.
Every dollar counts.
Every gift fuels hope.
Join us and be part of the solution for LGMD2I/R9.
Thank you for your generous support!