Vicky Robayna’s daughter, Liz, sadly died from a rare form of cancer aged 17. Vicky explains how, with the right support, there’s hope for families that their child can be comfortable during palliative care, allowing them to make memories and embrace life in the time they have.
Earlier this year, CCLG launched its new research strategy. Ashley Ball-Gamble, CEO of CCLG, explains what this means for children and young people’s cancer.
Rosie Lazar was diagnosed with acute lymphoblastic leukaemia (ALL) aged two in 1996. Now 32, she tells us about her cancer treatment as a child, what life looks like now, and why she wants to give back to charities like those that helped her.
Lewis Paget, now 26, was diagnosed with two different leukaemias at the same time as a teenager in 2016. Here, he describes the impact of this, and how it has influenced him to become a cancer researcher himself.
Michael Omotayo was diagnosed with retinoblastoma, when he was two years old in 1995. Now 32, he tells us about his journey from a young child with cancer to becoming a personal trainer and sports performance coach, including the challenges he’s faced and how he’s overcome them.
A family whose son was treated for leukaemia is raising awareness of the disease and funds for research into improving treatments for it.
Ezra was diagnosed with medulloblastoma, when six years old in June 2024. His mum, Rhiannon, shares his story.
Susie Aldiss talks about the top ten research priorities in childhood cancer and what's next for this project.
Hear from Professor Suzanne Turner about her research and how families are at its heart.
