In December 2014, my son, Felix, was diagnosed with Duchenne Muscular Dystrophy, a severe, muscle wasting disease. It's currently incurable and the prognosis is grim. However, there is real hope, mainly because of the incredible research and drug development work being funded by Duchenne UK. The future of thousands of kids depends on them being able to continue funding this work. This requires a lot of money, most of which comes from this event, so if I could ask you to please give as generously as you can. Thank you!