Our son, Felix, was diagnosed with Duchenne Muscular Dystrophy in October 2018, aged four years, one month. Duchenne is a severe muscle wasting condition, which is rare. Approx 2500 boys in the UK are living with the condition. Theres currently no cure, however, the research thats been conducted over the past six years is extremely promising, but more money is needed to make further research possible, and to find the cure for Felix and all the other children, living with the condition, as soon as possible.

Your support means the absolute world to us. All money raised goes to Duchenne UK to fund further research into finding a cure.

You can donate here or why not set up your own event and link to us!

Thank you,

Charlotte and Daniel