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.
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.
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.
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.
Dr Ren Manias, Consultant Paediatric Oncologist at Southampton General Hospital and Contact's new medical adviser
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.
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.
Professor Bruce Morland is a recently retired paediatric oncologist from Birmingham Children’s Hospital. Here, he tells us about his work as a chief investigator on a global clinical trial.
We published our first Research Impact Report this year to celebrate CCLG's progress towards finding a cure for children's cancer. As readers of Contact magazine, we are delighted to share extracts from this report in this 4-page supplement for Contact readers.
