Could starving brain tumours be a way of treating childhood cancer?
We all know that we need to eat to survive. However, we also know there are specific things that we need to eat in order to get the nutrients for our bodies to grow and repair.
We all know that we need to eat to survive. However, we also know there are specific things that we need to eat in order to get the nutrients for our bodies to grow and repair.
The launch of the final report of the Children’s Cancer Priority Setting Partnership (PSP) was marked recently with a special event in London (28 June).
Children’s Cancer and Leukaemia Group (CCLG) is delighted to announce two new research projects that will help further understanding of childhood acute lymphoblastic leukaemia (ALL).
Researchers used to just work on things that they thought were important to learn more about. Now, parents and patients are getting more involved and shaping research priorities...
Two men have raised almost £3,000 for Children’s Cancer and Leukaemia Group (CCLG) by cycling the entire length of Great Britain in just five days.
Rosie was diagnosed with acute lymphoblastic leukaemia (ALL) at the age of three. Her mum, Jenny, shares her story.
One of the most interesting things about quality of life is that it is different for everyone. It depends on your values, culture, and expectations. So, how can we learn what matters to children?
Cyclists Fighting Cancer (CFC) supports children and young people living with and beyond cancer in the UK by giving them new, lightweight bikes, specially adapted trikes and cycling equipment. Liz Pharoah, CFC trustee and cancer exercise specialist, tells us more.
Supershoes is a national charity that helps children and young people become active again after a cancer diagnosis. Its founder and CEO, Sarah White, tells us how it provides young patients with a pair of specially crafted shoes designed to encourage them to move.