Louise Bennett shares the story of her son Fred and her experience as a member of our Patient and Public Involvement Group. She explains how her involvement in shaping CCLG's research has enabled her to make a lasting difference for children and young people with cancer in the future.
This Childhood Cancer Awareness Month, we spoke to Katherine about her daughter Helena’s story, her experience as a member of CCLG’s Information Review Panel and other projects, and how getting involved has given her a sense of purpose.
Lisa Radcliffe is a member of CCLG's Patient and Public Involvement (PPI) Group, where she uses her lived experience to help researchers shape and improve their work.
Bertie was diagnosed with T-cell acute lymphoblastic leukaemia (T-ALL) in May 2024 on his 11th birthday. Bertie finished his treatment in June 2026.
Braidy was diagnosed with blood cancer in 2025 while pregnant. Here, she shares how she navigated treatment, while pregnant and as a new mum, and why she wants to raise awareness.
Oliver was diagnosed with Wilms tumour when he was one year old. His mum, Ceri-Anne, shares his story.
Darcey was diagnosed with acute lymphoblastic leukaemia (ALL) in November 2022 when she was just 17 months old. Her mum, Sophie, shares her story.
Alex Witton was diagnosed with Hodgkin lymphoma in May 2025 at 22 years old. This Teenage and Young Adult Cancer Awareness Month (TYACAM), she shares her story.
Layla Jane Bartlett was diagnosed with ovarian cancer in January 2025 when she was 22 years old.
