Our son Dexter was diagnosed with Duchenne Muscular Dystrophy (DMD) in 2017.  DMD is the most severe form of muscular dystrophy and it has no cure. When we found out we were completely hopeless until we found Duchenne UK, a charity committed to funding research into treatments for DMD and ending Duchenne for good. Filled with hope we started a Friends and Family Fund with them called Team Dex and so began our fundraising. It's been hard to raise money with Covid and lockdowns so we're really excited to take part in Team Dex's Virtual 5km and 10km and try to raise as much money as possible for Duchenne UK and help our son Dexter. 

Thank you dear friends ❤