Supporting Research Toward a Cure for Limb Girdle Muscular Dystrophy, Type 2i

Help Support Research to Find a Cure for Limb Girdle Muscular Dystrophy Type 2I

Limb Girdle Muscular Dystrophy Type 2I (LGMD2I) is a progressively debilitating disease caused by weakness and muscle wasting mainly in the shoulder and hip areas. This congenital disease is a rare form of Muscular Dystrophy. Over time, this excessive muscle wasting can result in cardiovascular, respiratory and overall physical complications typically beginning in early adolescence. To date, the CureLGMD2i Foundation (formerly known as The Samantha J. Brazzo Foundation) has provided over $900,000 to research, advocacy and awareness programs focused on LGMD2i/R9.

Please Help Support Research to Find a Cure for LGMD 2i
Please Help Support Research to Find a Cure for LGMD 2i
Please Help Support Research to Find a Cure for LGMD 2iDonate
Fundraising Events for CureLGMD2i
Fundraising Events for CureLGMD2i
Fundraising Events for CureLGMD2iFind Out More
Clinical Trials for LGMD2i/R9
Clinical Trials for LGMD2i/R9
Clinical Trials for LGMD2i/R9Find Out More

Our Community

LGMD Awareness Day

We celebrate LGMD Awareness Day on September 30th each year. Please take a look at the video below for how we are bringing this to forefront.

LGMD Awareness Day

We celebrate LGMD Awareness Day on September 30th each year. Please take a look at the video below for how we are bringing this to forefront.

LGMD EL-PFDD Coming Soon!

Share your voice with the FDA to facilitate a treatment for LGMD2i/R9! More info here: https://lgmdpfdd.com

LGMD EL-PFDD Coming Soon!

Share your voice with the FDA to facilitate a treatment for LGMD2i/R9! More info here: https://lgmdpfdd.com