Kyes 
DMD Jounrey

Our 9 year old boy Kye has Duchenne Muscular Dystrophy. We decided to share our Duchenne Journey. We hope you enjoy looking round our page and following our family's journey. Check out our latest blog. You can fill out our mailing list form and get updates when new blogs are available etc. On our How you can help page is info on making donations to help find a cure for Duchenne.