Finding freedom on two wheels
Chris Badcock’s son, Sam, was diagnosed with a brain tumour in 2019 when he was 11 years old. He tells us how cycling made a profound difference to his son's recovery and quality of life.
Chris Badcock’s son, Sam, was diagnosed with a brain tumour in 2019 when he was 11 years old. He tells us how cycling made a profound difference to his son's recovery and quality of life.
Kay Hunter Saber’s son, Ramsey, was diagnosed with leukaemia aged 14. She explains how they navigated his treatment and how writing helped her through his journey.
We asked the experts from the Haematology/Oncology Team at Sheffield Children’s Foundation Trust to share tips and advice on small steps that can be taken to support a child’s wellbeing during treatment.
Abby Maxwell was diagnosed with blood cancer aged 22 in 2023 and shares with us what helped her during her treatment.
Stacey Bark’s daughter, Florrie, was diagnosed with acute myeloid leukaemia aged five in 2022. Here, Stacey explains how their family navigated cancer and some of the serious complications of Florrie’s treatment and what resilience means to them.
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.