Nilson Family

Our youngest son, Henry, was diagnosed with Duchenne in August 2011 – shortly before his 3rd birthday. It was a fluke test that shocked even the doctors as it was […]

CureDuchenne Comment Letter to the Advisory Committee on Immunization Practices  for COVID-19 Vaccine Distribution

Dear Committee Members,    On behalf of  individuals living with Duchenne muscular dystrophy, their families, and caregivers served by CureDuchenne, I am writing to urge the Committee to include individuals with Duchenne in its recommendations for sub-populations to receive approved or authorized COVID-19 […]