Magazine articles list

Gayle Routledge, mum to Lewis who sadly died of cancer aged two in 2010 and founder of bereavement charity A Child of Mine, tells us how his memory inspires all that she does now.

Our research projects cover the whole cancer journey from learning about how cancer cells grow to improving everyday life for patients and survivors.

Sinead Wood's son Cillian finished treatment for T-cell lymphoblastic lymphoma last summer. She writes on how it took time for her and her family to adjust to life after treatment, and offers advice to others trying to do the same.

Dr Rachel Cox, is a consultant paediatric oncologist and Chair of CCLG’s Late Effects Group. She tells us what late effects are, and how the work of the group is helping to improve the quality of life for survivors of childhood cancer.

The clinical lead nurse at Bristol Haematology and Oncology Centre and Chair of TYAC talks to us about his career, plans and interests.

Naomi Shefford-Thomas, CCLG Information Executive and mum to Phoebe, who underwent almost four years of treatment for neuroblastoma, answers your questions.

Imaging is central to diagnosing and monitoring solid cancers and scans are a key part of the patient and family journey. Different types of scans such as CT, MRI and PET, have all become commonplace in hospitals throughout the UK and children benefit from the accurate high-quality images they produce.

Prof Louis Chesler leads the Paediatric Oncology Experimental Medicine (POEM) Centre at the Institute of Cancer Research (ICR). He tells us about some of the exciting digital innovations that have the potential to transform childhood cancer treatment.

Dr Bob Phillips, Senior Academic Consultant at University of York, Consultant Paediatric Oncologist at Leeds Children’s Hospital and CCLG member, writes...