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In this section of the resource you will find information about the basics of palliative care for children with cancer.

Palliative care for children and young people with life-limiting conditions is an active and total approach to care, from the point of diagnosis or recognition, embracing physical, emotional, social and spiritual elements through to death and beyond.

This section is designed to give a brief overview of the medical management of the main symptoms experienced in the child or young person with advanced cancer and a brief insight into the main issues families face.

Information and suggestions for talking about death and dying.

In most cases, the child or adolescent with cancer will have been cared for by the same Consultant, Paediatric Oncology Outreach Nurse Specialist (POONS) and CLIC Sargent Social Worker (CSSW) from diagnosis through to death.

In this section of the resource you will find information about some aspects of psychosocial support.

Bead trails are a popular and useful way for a child or young person and their family record their cancer journey.

It is well recognised that having a child or adolescent with cancer puts a large financial strain on a family unit with the extra costs involved.

Pets are an important part of the family for many people. Most children and young people with cancer can and should keep their pets.

Play is a freely chosen activity that can be fun and relaxing. In the hospital setting, play is used to bridge the gap between home and hospital. Play helps children’s cognitive development, understanding of rules, social interactions and ability to work through difficult situations.