Ellie Waters, 20, is a digital content creator who was diagnosed with rhabdomyosarcoma, aged 14. She tells us how she began creating digital content to share her experiences and help raise awareness of childhood cancer and its effects.
Dr Bob Phillips, Senior Academic Consultant at University of York, Consultant Paediatric Oncologist at Leeds Children’s Hospital and CCLG member, writes...
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.
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.
