Cameron’s Journey

Hi, it’s Cameron’s mummy here, Natalie.

Our beautiful 3 year old son was recently diagnosed with Duchenne Muscular Dystrophy. A heartbreaking, muscle wasting disease that in short, will end in disability and a shorter life span.

My husband and I are not accepting this horrific news. Instead, we are doing everything in our power to raise awareness, funds and support for our son.

Already, there are some ground breaking research trials going on for Duchenne but like anything, it costs money.

We are unsure what lies ahead for Cameron but we do need money now so that if we need to travel to London or America to see Duchenne Specialists, we don’t have to wait about, we have the money here and now.

Contribute what you can and if you can.

Thank you so much,

Natalie