Bryan Arnold of Anchorage, Alaska, educates people about his degenerative disease, Duchenne muscular dystrophy (DMD). During his junior year of high school, he produced this...
BrainPOP's beloved animated duo, Tim and Moby, present the topic of Duchenne in this short, animated movie. Produced in partnership with Parent Project Muscular Dystrophy,...
Short video on Muscular Dystrophy and its Summer Camp. Muscular Dystrophy is a rare muscular disease still without a cure. My mother has Muscular Dystrophy,...
Sophie has a rare form of muscular dystrophy called Emery-Dreifuss. She is celebrating her 13th Birthday and is Vice President of her student council! She...
www.chaitanyastemcell.com stem cell therapy for Duchenne Muscular Dystrophy (DMD) in Chaitanya Stemcell Therapy Center India In this video, it shows Duchenne Muscular Dystrophy (DMD) patient...
