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.
Naomi Shefford-Thomas, CCLG Information Executive and mum to Phoebe, who underwent almost four years of treatment for neuroblastoma, answers your questions.
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.
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.
The clinical lead nurse at Bristol Haematology and Oncology Centre and Chair of TYAC talks to us about his career, plans and interests.
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.
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+.
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.
