Special Named Fund stories
News and updates about CCLG's Special Named Funds.
News and updates about CCLG's Special Named Funds.
Alex Witton was diagnosed with Hodgkin lymphoma in May 2025 at 22 years old. This Teenage and Young Adult Cancer Awareness Month (TYACAM), she shares her story.
Teenagers and young adults with cancer know what they need - faster diagnosis, age-specific support, better treatments - but their voices often go unheard. We want to change that.
In this section we look at life a few years after your child has died.
You play an important role in supporting children with a central nervous system (CNS) tumour at home. The family will have all the contact details for their cancer care team, who may well have contacted you directly to provide an aspect of care in the home.
Teenagers and young adults with cancer have distinct needs. The CCLG Teenage and Young Adult Cancer Research Centre aims to address them.
Sign up to receive email updates on the progress of the Child Cancer Smart campaign.
A major new initiative designed to address the long-standing underfunding of research focused on teenagers and young adults with cancer, particularly in the psychosocial aspects of care, is set to launch.
Little Princess Trust (LPT) researchers have discovered a new method that bone cancer can use to secretly fight the immune system
CCLG is excited to be partnering with The Bone Cancer Research Trust again, to fund research focused on Ewing sarcoma and osteosarcoma.