Expertise. Progress. Community.
A charity dedicated to creating a brighter future for children and young people with cancer.
Who we are
Expertise.
Without CCLG, I don't think I could do my job as well as I do. Being a member enables us to give the best care we can for our patients and their familiesDr Nicky Thorp, Consultant Clinical Oncologist, The Christie
Expert clinical work
Together with our professional members, we shape better treatment and care—developing guidelines, sharing expertise, offering advice, leading groundbreaking research, and creating essential resources and education for professionals.
Advising government policy
We use our expertise and influence to make things better. By campaigning, advocating and working alongside governments, the NHS, and other organisations, we’re pushing for progress and shaping a brighter future for young lives.
Trusted patient information
We provide trusted information and guidance for children and young people with cancer, their families, and everyone supporting them. Our expertise helps them navigate the challenges of cancer and its impact, offering reassurance and clarity when it’s needed most.
Progress.
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84 %
survival rate
in children compared to 20% in the 1960s, thanks to advances in research
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125
research projects
funded in the last ten years with the support of research partners
Community.
Leading powerful collaborations
Child Cancer Smart
A collaborative project which will measure, understand and improve the time it takes to diagnose children and young people with all cancers across the UK.
Children’s Cancer Priority Setting Partnership
Bringing together patients, families, professionals and families to improve outcomes for every type of cancer and ensure every child and young person goes on to lead a long, healthy, and happy life.
Latest News & Updates
Supporting siblings to build connections with special residential trips
Barretstown offers free, specially designed camps and programmes for children living with cancer and other serious illnesses and their families. Here, Siobhan Kavanagh, its Director of Medical and Programme, tells us about their support for siblings.
I’ve learnt so much about the quiet strength of siblings
Elizabeth’s daughter, Sarah, who also has Down syndrome, was diagnosed with leukaemia in 2016, aged 15. Here, she tells us how her youngest daughter, Hannah, then eight, provided support to her sister, and about the challenges of balancing family life…
"It was confusing for her, but we did our best to be open and honest”
Rosa Kaminska’s son, George, was diagnosed with T-cell lymphoblastic lymphoma in December 2022 aged six. Here, she explains the impact of this on George’s sister, Anna, what helped them as a family during his early treatment, and offers advice to others.