Search

Professor Bernadette Brennan, Consultant Paediatric Oncologist, tells us what rare childhood cancers are and how they are treated.

Collaboration, teamwork and partnerships are vital to childhood cancer research. Ellie Wilkinson, CCLG's Research Communications Executive, explains how charities are coming together and researchers are linking up to work towards a better future for children with cancer.

Dr Ren Manias, Consultant Paediatric Oncologist at Southampton General Hospital and Contact's new medical adviser

Dave Hartley’s daughter Evie was diagnosed with a brain tumour, aged 12. Here, he tells us how the keen cyclist received support from her club, town and wider cycling communities, and how, in turn, she inspired them to achieve incredible things.

Toria Pick, Family Support Worker at PASIC explains about her career so far, what her role involves, what her proudest moment is , what her job means to her and how families can find out about accessing a family support worker.

My child has cancer... what happens next?

Leanne Connor & Dan Blamires are members of ‘Unity: The After Cure Choir’. They tell us how the choir provides patients from the Leeds long-term follow-up (LTFU) service with a warm and welcoming space to come together, have fun and support each other.

Naomi Shefford-Thomas is CCLG’s Information Executive and mum to Phoebe, who was diagnosed with neuroblastoma in 2016. She tells us how invaluable online support from other parents helped her navigate her daughter’s treatment and offers advice to others looking to find the same.

Ross Long was diagnosed with non-Hodgkin lymphoma in 2013. He tells us about those who supported him and how he plans to write a book to lessen the isolation of other young people diagnosed with cancer.

Claire Farish’s son, Max, was 11 years old when diagnosed with cancer in May 2021. She explains how her family initially felt isolated after his diagnosis, but eventually found hope, support and understanding after reaching out.