COALITION TO CURE CALPAIN 3 wrote -
Limb Girdle Muscular Dystrophy Type 2A (LGMD2A) results in a deficiency of the calpain 3 enzyme, robbing individuals of their muscle strength and taking them from full mobility to wheelchair dependency, typically within 11-28 years after the onset of symptoms. Coalition to Cure Calpain 3 (C3) is committed to curing this rare neuromuscular disease by funding high potential research and clinical trials as we educate the global community about LGMD2A.
If you donate to C3, we will send you 3 wristbands: 1 to wear yourself and the other 2 to share with friends to help us raise awareness of this "orphan disease"...
3 for C3!