Defeating Duchenne Muscular Dystrophy

It’s hard to fathom why certain children receive life-altering diagnoses. Pediatricians simply want to help, and that help usually comes in the form of early diagnosis. Duchenne muscular dystrophy, otherwise known as Duchenne or DMD, is the most common fatal genetic disorder diagnosed in childhood, affecting approximately one in every 5,000 live male births. Early screening and identification can mean quicker access to care, early intervention programs and special education resources. Thanks to early diagnosis and advances in care, life expectancy is increasing.

Our guest joining us to discuss diagnosing and treating DMD is Michele Yang, MD, who specializes in pediatric neurology and neuromuscular medicine at Children’s Hospital Colorado. She is also an associate professor of pediatric neurology at the University of Colorado School of Medicine.

In this episode, our pediatric neurology expert discusses:

• How diagnosis of DMD has changed over the years.
• Understanding the new, advanced treatments that exist.
• Tips and tricks for primary care providers to utilize.
• Realistic outcomes for these kids with DMD.

Duchenne muscular dystrophy resources mentioned in the episode include:

• Parent Project Muscular Dystrophy 
• CureDuchenne 
• Muscular Dystrophy Association