
Sophie's story
Sophie was ten years old when she was diagnosed with a Wilms tumour on her left kidney. Her mum, Rebecca, shares their story.
Sophie was ten years old when she was diagnosed with a Wilms tumour on her left kidney. Her mum, Rebecca, shares their story.
Finley was diagnosed with acute lymphoblastic leukaemia (ALL) in December 2018 when he was seven years old. His mum, Natasha, shares his story.
The Little Princess Trust (LPT) has announced three new research projects will be funded by its prestigious Innovation Grant. Awarded in partnership with Children’s Cancer and Leukaemia Group, LPT’s Innovation Grant aims to fund promising and inspired new research ideas.
Mollie was diagnosed with parameningeal embryonal rhabdomyosarcoma in 2018, just one month before her third birthday. Her mum, Fiona, shares her story.
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.
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.
Dr Guy Makin, Senior Lecturer in Paediatric Oncology at the University of Manchester and Honorary Consultant Paediatric Oncologist at Royal Manchester Children’s Hospital, talks to us about his work.
Helen Pearson and Katie Johnson, co-chairs of the National Neuroblastoma Nursing Group (NNNG), tell us more about how they have developed a range of animation videos to help parents make decisions about their child’s treatment as part of a neuroblastoma clinical trial