Families fund vital new research into rare blood cancer
New research into a rare type of leukaemia has been funded, thanks to several Children's Cancer and Leukaemia Group (CCLG) Special Named Funds.
Family raises £100,000 for children’s cancer research in memory of kind-hearted son
A family fundraising for children’s cancer research in memory of their 16-year-old son fulfilled their promise to him that they would raise £100,000 before the second anniversary of his death.
Stanley's story
Stanley was diagnosed with group A posterior fossa ependymoma, a type of childhood brain tumour, when he was six years old. His mum, Kirsty, shares his story.
Connie's story
Connie was diagnosed with high-risk medulloblastoma, a childhood brain tumour, in October 2022. Her mum, Tina, shares her story.
New research highlights significant gaps in public awareness of signs and symptoms of cancer in children and young people
Only 32% of adult survey respondents felt confident in recognising cancer signs and symptoms in children, teenagers and young adults, according to newly published research.
How the variability of neuroblastoma makes it harder to cure
Cancer cells can have differences in how they survive, respond to treatment, and behave. This variability can help cancer cells survive and adapt, but it also makes doctors’ jobs much harder.
Raeyah's story
Raeyah was diagnosed with stage four, non favourable Wilms tumour at the age of three. She sadly passed away, aged four, in 2023. Her mum, Becky, shares her story.
Ro's story
Ro Cartwright was diagnosed with cancer in 1968, aged eight. Now 63, she reflects on her experiences, including the difference in treatment and care seen today, and how more has come to be learnt about the long-term effects of children’s cancer.
Charlie's story
Sarah Jackson’s daughter Charlie was diagnosed with leukaemia in 2011 when aged three. Here, Sarah tells us about the long-term effects of Charlie’s cancer and her treatment.