DMD Voices

The latest insights and perspectives from people who have lived and struggled with DMD

Sarka Palouckova DMD doesn’t wait, and neither can families: A grandmother’s plea for better guidance
Sarka Palouckova The day hope for DMD knocked at my door, with a bill in hand
Sarka Palouckova Left in silence: Families facing rare diagnoses need better support
Conor McAuley What it was like to be diagnosed with Duchenne muscular dystrophy at 3 years old