Jack was born in November 2015. After years of hospital visits and unanswered questions, we finally got a diagnosis in 2019: Duchenne Muscular Dystrophy. It changed everything—but Jack’s strength and spirit continue to inspire us every day.

Muscular Dystrophy UK is the charity for the 110,000 children and adults living with muscle-wasting conditions in the UK. There's currently no cure, and it many cases, it limits lives. MDUK do vital work in funding pioneering research into treatments and cures as well as providing vital information, advice, resources and support for individuals and families living with these conditions.

All donations, big or small, are greatly appreciated. Thank you!