When a parent hears their newborn or young child has a genetic condition that could affect the rest of their lives, they may be scared, confused, and have questions about what to do next. Research in gene therapy has led to significant changes in how doctors work with families on those questions.
This hour, we sit down with two local mothers who share their families’ stories of accessing care for their children, and we’re joined by the experts who provide that care.
Our guests:
- Emily Hessney Lynch, parent of a child who received gene therapy
- Kate White, DPT, physical therapist in the Orthopedics Department at the University of Rochester Medical Center, and creator of Team Teddy 5K, an annual fundraiser for Duchenne Muscular Dystrophy research
- Samuel Mackenzie, M.D., Ph.D., assistant professor in the Departments of Neurology, Neuroscience, and Pediatrics; and the Center for Health and Technology at the University of Rochester Medical Center
- Bo Hoon Lee, M.D., assistant professor in the Departments of Pediatrics and Neurology, Child Neurology at the University of Rochester Medical Center