"Our Mission is Supporting Young people Lives like Duchenne Muscular Dystrophy.

At the heart of our mission is a deep commitment to young people aged 16-25 with life-limited Duchenne Muscular Dystrophy and their families. We understand the profound challenges during the transition from children to adult services. Our aim is to bridge the gaps in support, end-of-life care, and bereavement resources. Inspired by Bradley's Journey. Our dedication is born from personal experience. The lack of support we faced during our difficult time before Bradley passed away highlighted the urgent need for better resources and guidance. In Bradley's memory, we strive to ensure no family faces this journey alone."