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.
Teens Unite Fighting Cancer supports teenagers and young adults living with cancer and its lasting effects. Roxanne Lawrance, CEO, explains how it aims to create a community so patients can support each other as they begin to rebuild their lives
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.
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.
The Children’s Cancer Priority Setting Partnership (PSP) aims to identify gaps in research and ‘unanswered questions’ on children’s cancer by including patients and parents. Susie Aldiss, Prof Faith Gibson and Dr Jess Morgan, of the project team, explain more.
Katy Jones' daughter Eden was three years old when she was diagnosed with leukaemia in July 2017. She explains some of the things her family considered before deciding on entering into a clinical trial.
Carrie Wright’s daughter, Lucy, was diagnosed with neuroblastoma in August 2018. She writes on participating in the international MiNivAN clinical trial and offers advice to others faced with making decisions about their child’s treatment.
