Life was turned upside down for us and Samuel’s two brothers when we were told he had a brain tumour. The tumour was removed in a long operation, but a few days later, we were given the devastating news that it was cancer. Soon after, we found out that it had spread and that there was another spot of disease elsewhere in his brain, making his condition high-risk of relapse after treatment, rather than the standard risk we were originally told.
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.
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.
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 was diagnosed with nephroblastoma, also known as Wilms tumour, at the age of four. Her mother, Abby, shares her story.
Mason was diagnosed with a brain tumour in February 2024 when he was seven years old.
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...
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 was six years old when she was diagnosed with leukaemia in 2020. Her mum, Victoria, shares her story.
