In September ‘25, our world changed when our amazing son, Louie, was diagnosed with Duchenne Muscular Dystrophy after 3 years of uncertainty. It was earth-shattering at first, but as we’ve learned more, we’ve found hope, because research is advancing every day.

Louie is the most imaginative, funny, and creative little boy you could meet. He loves superheroes, Minecraft, football (Newcastle, just like daddy of course!) and dreams of making his own action movies one day. Despite challenges with his legs, he faces everything with courage and laughter. The true definition of brave.

Together with MDUK, our family fund ‘Brave Like Louie’ aims to fund life-changing research and support Louie’s future needs.

We’re inviting you to be part of Louie’s story…to spread hope, strength, and love.

Let’s defeat Duchenne!