CureLGMD2i Foundation
Providing Advocacy, Spreading Awareness, Supporting Scientific Research and Drug Development with the Goal of Finding a Cure for LGMD2I/R9
CureLGMD2i Foundation Instagram
CureLGMD2i Foundation Instagram
CureLGMD2i Foundation Facebook
CureLGMD2i Foundation Facebook
CureLGMD2i Foundation YouTube
CureLGMD2i Foundation YouTube
Registration Link for Discussion on Genetic Testing
Registration Link for Discussion on Genetic Testing
Please join us for an informative discussion on genetic testing and its importance for families impacted by conditions like LGMD2I/R9. Dr. Weihl, an LGMD specialist, along with his associate Amanda from Washington University in St. Louis, both experts in genetic variant resolution, will share their work in developing a database of LGMD mutations, including variants of unknown significance (VOUS).
HHS - Advancing Innovation on Rare Disease Therapies - YouTube
HHS - Advancing Innovation on Rare Disease Therapies - YouTube
2026 European LGMD2I/R9 Patient and Family Conference Registration Page
2026 European LGMD2I/R9 Patient and Family Conference Registration Page
CureLGMD2i E-Newsletter Sign up
CureLGMD2i E-Newsletter Sign up
Donate to Support CureLGMD2i
Donate to Support CureLGMD2i
CureLGMD2i Merch Shop
CureLGMD2i Merch Shop
2025 Annual Report
2025 Annual Report
Facebook
Facebook
Facebook
Instagram
Instagram
YouTube Video Collection
YouTube Video Collection
Visit our CureLGMD2i Website
Visit our CureLGMD2i Website
Join the LGMD2i Facebook Group
Join the LGMD2i Facebook Group
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