News & Updates

Brad Gudger, diagnosed with leukaemia as a 19-year-old, tells us how he has used his own experiences to establish a charity and launch an app for cancer patients aged 18+.

Rachel Corbett’s daughter, Suki, was diagnosed with acute lymphoblastic leukaemia (ALL) in January 2017, aged four. Rachel writes about spending Christmas in hospital and how the experience has changed how her and her family think of it.

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 Annmarie Jeanes, Consultant Paediatric Radiologist at Leeds Children’s Hospital, explains the different types of imaging your child may experience at the time of diagnosis, during treatment and follow-up

Sheila Cartwright, one of the first CCLG members and retired paediatric radiation oncologist, reflects on her career, and explains how LinkedIn allows her to keep up with developments in childhood cancer and reconnect with former patients.

With the COVID-19 pandemic delaying many of its plans, Teenagers and Young Adults with Cancer (TYAC), CCLG’s sister organisation, has revisited its ambitious 2020-2025 strategic plan. Ashley Ball-Gamble, CEO of TYAC and CCLG, explains more.

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.

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.