Magazine articles list

Adapting to life after treatment can be difficult, and patients and their families may experience a range of different emotions as a result.

Dr Ed Cheeseman, Consultant Paediatric Pathologist and Chair of CCLG’s Biological Studies Steering Group, explains the difference between ‘normal’ cells and cancer cells, how the latter develop, and what they do to the body.

Sarah Mcdonald’s daughter Summer was diagnosed with leukaemia in 2012. She writes on what life looked like for Summer’s sister, Kya, during treatment.

Dr Rob Jobe is a clinical psychologist at Health in Mind, Birmingham Children’s Hospital. He spoke to parents about some of the emotions they experienced during their child’s cancer journey and offers advice on managing such feelings.

Helen Ball’s daughter Emily has recently finished treatment for acute lymphoblastic leukaemia (ALL). Helen tells us about what life has looked like for her family since Emily’s diagnosis, and how nature and the outdoors has helped them.

Chloe Hunt was diagnosed with neuroblastoma in 2010. She describes the challenges she faced adapting to a ‘new normal’ both during and after treatment, and how she overcame them.

This year, a new cancer statistics report for children, teenagers and young adults was published. This is the first report for almost a decade covering the whole of the UK and the first that covers both children’s and teenage and young adult cancers. With input from CCLG professional members, the report was shared at our Winter Meeting in February, and will help us to understand progress in the management of these cancers. Here are some key figures from the report:

Research Fellow at the University of Nottingham and CCLG member, talks to us about her work

Sam Behjati divides his time between clinical work at Addenbrookes Hospital in Cambridge and research at the nearby Wellcome Sanger Institute.