Duchenne educational resources.
Duchenne community events.
Duchenne advocacy organizations often sponsor or participate in events that may be of interest to you. Find out more through the organizations listed below.
From Family and Caregiver Workshops to sporting events and fundraisers, Cure Duchenne provides ample opportunity to connect with others in the Duchenne community.
Jett Foundation empowers people and families impacted by Duchenne muscular dystrophy through the development of transformative programming, educational opportunities, and ongoing support for every stage of a Duchenne journey.
Parent Project Muscular Dystrophy hosts events that provide opportunities for families, caregivers, and those living with Duchenne to gather, build support networks, and discuss all topics Duchenne.
Duchenne patients who receive VYONDYS 53 must have a genetic test that shows a mutation in the dystrophin gene that can be treated by skipping exon 53. Your child's doctor is best equipped to determine if your child’s mutation is amenable to treatment with VYONDYS 53. We’ve developed a Doctor Discussion Guide to help you start that important conversation.
We developed SareptAssist, our patient support program, to help patients start and stay on therapy. You’ll have support at every step—from managing insurance approvals to coordinating drug delivery. How SareptAssist can help.