Philippa's story
Philippa was just two years old when she was diagnosed with Langerhans cell histiocytosis (LCH), a cancer-like disease. Her mum, Claire, shares her story.
Sussex man plans to take on huge fundraising challenge in memory of daughter
Jamie BartlettBundy, from Hassocks, is taking on the challenge in memory of Pearl, who passed away in 2017 after being diagnosed with a form of bone cancer called Ewing sarcoma.
‘My work experience at a brain tumour research lab’ with Ellie Brattan
After Ellie's younger sister was treated for cancer in 2019, she decided on a career in cancer research. We caught up with Ellie after her work experience in a childhood cancer research lab...
Scarlett-Anne's story
Scarlett-Anne was diagnosed with nephroblastoma, also known as Wilms tumour, at the age of four. Her mother, Abby, shares her story.
Mason's story
Mason was diagnosed with a brain tumour in February 2024 when he was seven years old.
CCLG Research Talks: How do we get the right doses of cancer treatment?
Dr Shelby Barnett shares how research is improving chemotherapy for children.
Spotlight on GOSH – how are our researchers working to help children with cancer?
In the UK and Ireland, over 100 childhood cancer researchers have been funded through CCLG. But what are they working on? Let's take a trip to Great Ormond Street Hospital to find out...
Special Named Fund helps CCLG fund new ependymoma research
Children’s Cancer and Leukaemia Group (CCLG) has funded a new research project which aims to find a faster way to detect relapse in an aggressive type of brain tumour.
Niamh's story
Niamh was six years old when she was diagnosed with leukaemia in 2020. Her mum, Victoria, shares her story.