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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.

Karen and Andrew Phillips were inspired to establish their own charity after their son Harry was helped through his treatment for leukaemia by a special aid. Here, Karen tells us more.

Sarah Turner and J’nae Christopher are assistant psychologists within Health in Mind at Birmingham Children’s Hospital. They explain that for a child going through treatment, to be given choice and control over even seemingly small things, can be of real value.

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.

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.

Consultant Clinical Oncologist and CCLG Trustee talks to us about his career and interests

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.

Emily Zobel Marshall describes some of the choices her family made after her daughter, Rose, was diagnosed with leukaemia in March 2018

When I agreed to write this column in this edition of Contact, themed on ‘Choices’, I thought it would be easy. But it wasn’t – just like the choices that families have to make.

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.