Oliver's story
Oliver was diagnosed with Wilms tumour when he was one year old. His mum, Ceri-Anne, shares his story.
Oliver was diagnosed with Wilms tumour when he was one year old. His mum, Ceri-Anne, shares his story.
Little Princess Trust (LPT) researchers have found that children treated in childhood cancer treatment centres across the UK and Ireland all have the same high chance of recovery.
Research takes time, so it can be hard to understand what progress is being made. But what if we could follow a single idea through the research journey?
A father is taking part in the Great North Run to raise funds for children’s cancer research in memory of his two-year-old son.
Wilf was diagnosed with stage 4 Wilms tumour in 2022 when he was six years old. His mum, Tori, shares his story.
Scarlett-Anne was diagnosed with nephroblastoma, also known as Wilms tumour, at the age of four. Her mother, Abby, shares her story.
In the UK and Ireland, over 100 childhood cancer researchers have been funded through CCLG. But what are they working on? Let's take a trip to Great Ormond Street Hospital to find out...
April is Teenage and Young Adult Cancer Awareness Month. We caught up with one of TYAC’s researchers, Dr Nicola Hughes, to learn more about cancer research for young people.
Hear from Professor Matthew Murray about Wilms tumour and improving kidney cancer care.