Casma Therapeutics Inc. has gathered $50 million in a Series B financing round to propel a treatment for the genetic disease Duchenne muscular dystrophy toward clinical trials. New investor Column ...

INDIANAPOLIS (WISH) — It’s a devastating diagnosis that changes a child’s life forever, Duchenne muscular dystrophy, or DMD, is a rare and fatal genetic disease that primarily affects boys.

INDIANAPOLIS — A local mom is pushing for a rare and deadly disease to be added to Indiana's newborn screening panel. Duchenne muscular dystrophy affects at least 1 in 5,000 male births each year.

This is the story about an Indianapolis neurologist, Charles Bonsett, M.D., who believes he discovered an effective treatment for Duchenne muscular dystrophy over 50 years ago. Unfortunately ...

More than 50 kids can now say they are friends with a few Indianapolis firefighters. The department and the Muscular Dystrophy Family Foundation hosted their annual holiday party. The event ...

This is the story about an Indianapolis neurologist, Charles Bonsett, M.D., who believes he discovered an effective treatment for Duchenne muscular dystrophy over 50 years ago. Unfortunately ...