As part of Cat Macleod’s role as a Young Lives vs Cancer social worker, she helps families plan and access trips and holidays while their child is on treatment. She explains the positive impact these breaks can have, and things to consider beforehand.
Theatremaker Toby Peach tells us about his new project in collaboration with Carmen, who was diagnosed with a brain tumour aged 7.
Eating well during treatment is really important as a well-nourished child is able to cope better with their treatment and fight infection. It will also help their body repair healthy body tissues that have been damaged by chemotherapy or radiotherapy. By Louise Henry, Paediatrics Senior Specialist Dietitian at Royal Marsden
Dr Bob Phillips describes how decisions are made in children’s cancer care, and how it can feel when the choices aren’t so obvious.
Emily Zobel Marshall describes some of the choices her family made after her daughter, Rose, was diagnosed with leukaemia in March 2018
CCLG’s trailblazing and innovative Special Named Funds (SNFs) programme provides a positive platform for families, friends and communities to raise funds in the name of a child affected by cancer. Carly tells us more.
Josh Hill was diagnosed with acute lymphoblastic leukaemia (ALL) in September 2004. Now 21, he tells us how he chooses to allow his experiences to drive what he does, rather than control him.
Our supporters help us to continue our important research through fundraising and donations, with many of our research projects supported by our Special Named Funds.
Shielding...a term unknown until March 2020! Tash Larcombe, whose nine-year-old son, Finley, has leukaemia, writes on what shielding has been like for her and her family.
