Louise Robinson, Neuro-Oncology Outreach Nurse Specialist at East Midlands Children’s and Young Persons’ Integrated Cancer Service, tells us about educational support for young brain tumour patients.
The specialist learning mentor for the Medical Needs Teaching Service (MNTS) at Leeds Children’s Hospital (LCH), talks to us about his role supporting young cancer patients
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.
Consultant Clinical Oncologist and CCLG Trustee talks to us about his career and interests
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.
Alexander Clarke was diagnosed with a soft tissue sarcoma aged 19, meaning he was old enough to make his own treatment choices. His mum Denise describes how he helped lessen their worries by involving them throughout, even when there were no further treatment options left for him.
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.
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.
