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.
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.
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.
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.
Adapting to life after treatment can be difficult, and patients and their families may experience a range of different emotions as a result.
Catrin Bayliss is a health play specialist at Cardiff and Vale UHB.
Steph Hall is a senior children’s cancer nurse at Leeds Children’s Hospital (LCH). She tells us what life looked like on a children’s cancer ward before COVID, what it’s looked like during the pandemic, and what it’s looking like now.
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.
