Engage is a first of its kind national initiative designed to ensure that the voices of children, young people and families affected by cancer drive meaningful change across the sector.

Solving Kids’ Cancer UK and Neuroblastoma UK are proud to have jointly awarded £50,827 over five years to fund UK participation in SIOPEN Bioportal

Nick Bird, Chair of Trustees at Solving Kids' Cancer UK, contributes to a new Lancet article on accelerating childhood cancer drug development.

We have published a statement recognising the sensitive nature of the BBC documentary series The Mother of All Cons and the related media coverage, outlining how we support families affected by childhood cancer.

Today (April 1) marks the first day of Teenage and Young Adult Cancer Awareness Month (TYACAM) – an opportunity for charities and the young people we support to come together and raise awareness.

Neuroblastoma parent and Solving Kids' Cancer UK trustee, Helen, shares how she grappled with this difficult decision. Her son Michael was diagnosed with high-risk neuroblastoma in 2021.

Published in February 2026, England's National Cancer Plan includes a dedicated chapter on children and young people’s cancers for the first time.

This new grant will fund up to three pre-clinical studies into new and improved drug combinations for treating relapsed neuroblastoma.

We were honoured to present Clinical Oncologist Dr Mark Gaze with the inaugural and prestigious Dr Audrey Evans Award at our annual Christmas Concert.