About us

This family fund has been set up by Felix's Mommy and Daddy, Charlotte and Daniel.


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. There's currently no cure, however, the research that's 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.


Thank you,

Charlotte and Daniel


Support us

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