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OUR STORY
On May 13, 2020, while the world was focused on COVID, our lives changed forever, we were told our six-year-old son, Dylan, had an incurable brain tumor. The shock quickly turned into survival mode: how could we give Dylan the best fighting chance? As parents, we felt powerless, reduced to a diagnosis without a plan to support him beyond treatment. When we asked the consultant what we could do, the response was, “You’re already doing all you can.”
While I knew food couldn’t cure Dylan, I saw firsthand how nutrition gave him strength, energy, and precious moments of childhood normality. His blood work remained strong, and he continued to thrive despite his condition. Throughout his treatment, I was shocked at the amount of sugar routinely offered to him, knowing that it could weaken the immune system and fuel cancer growth.
This experience reinforced the importance of good nutrition during treatment. We know that food alone can’t change the course of cancer, but we also know that nourishing a child’s body can make a difference in their overall well-being. For Dylan, a balanced, nutrient-rich diet gave him extra months of feeling strong and full of life.
Now, as a family, we are passionate about helping others on this journey. No child should face cancer without access to good nutrition, and we are committed to supporting as many families as possible, helping children feel their best and empowering parents to take an active role in their child’s health.

MEET THE TEAM
Louise Long
Founder & Dylan’s Mummy
Fiona Stirling-Aird
Trustee
Huw Davis-Evans
Trustee and Treasurer
Sue Clark
Chair of Trustees
Dan Clark
Trustee
Kelly Terranova
Social Media & Marketing
Jacqui McDermid
Trustee




















