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Alex Brownsdon, 40, is a research nurse and children's cancer survivor. She tells us about the impact of her cancer, the value of peer support and the importance of research.

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Lola-Rose was diagnosed with a Wilms tumour when she was three years old. Her mum, Jodie, shares her story.

Oscar was diagnosed with acute lymphoblastic leukaemia (ALL) when he was three years old. His mum, Philippa, shares his story.

Lucie was diagnosed with Wilms tumour in October 2021 when she was five years old. Her mum, Leonie, shares her story.

Cancer doesn't end when you finish treatment. Even after the cancer cells are long dead, the long-term effects of childhood cancer and its treatment remain. So, what are they?

We talked to Scott to find out how he is using his experiences of childhood cancer to improve research and advocate for the voices of patients.

We now lead one of the UK’s largest childhood cancer research networks, thanks to our partner charities and to your fantastic support. Find out what your support has achieved...

People often say that childhood cancer is rare - but is this accurate? Why parents, families, and people who have had cancer often prefer not to use the term rare.

There is a lot more to research than just scientists in white lab coats. We caught up with some of the amazing parents who help shape the direction of childhood cancer research.