Following a childhood cancer diagnosis, parents may find relationships with those around them change, while they may also develop a number of new relationships during their child’s treatment. Here, Dr Amandeep Samrai, Consultant Clinical Psychologist in Paediatric Oncology at Nottingham Children’s Hospital, talks about how relationships can be both helpful and challenging during childhood cancer treatment.
Kay Lewis’ daughter, Maisy, was diagnosed with retinoblastoma in both eyes when she was nine months old. Kay explains what helped them after treatment, and how Maisy continues to inspire her.
Caroline Cleaver is a proton beam liaison nurse at Manchester Children’s Hospital and CCLG member, whose twin sister was diagnosed with leukaemia when they were 19 years old. She tells us how this inspired her career in children’s cancer nursing and what helps her build relationships with patients and families under her care.
Teens Unite Fighting Cancer brings together teenagers and young adults living with cancer and its lasting effects. Its CEO, Roxanne Lawrance, explains how surrounding yourself with others in a similar situation can often be helpful during cancer and in the years that follow, and how Teens Unite helps young people do this.
Kelly Scott was diagnosed with non-Hodgkin lymphoma when she was a teenager in 2001. Now working for Teenage Cancer Trust, she explains how this affected her relationships with her peers and how some simple acts of kindness helped support her.
Sophie was diagnosed with acute lymphoblastic leukaemia (ALL) in April 2021 at the age of seven. Her mother, Tanya, shares her story.
Today (1 September) marks the beginning of Childhood Cancer Awareness Month (CCAM). This year, in addition to raising awareness of childhood cancer and its signs and symptoms, CCLG is shining a light on research and how, without it, progress in its treatment and care would not be...
People often say that childhood cancer is rare - but is this accurate? Why parents, families, and people who have had cancer often prefer not to use the term rare.
Samuel Priestley was 14 years old when diagnosed with pilocytic astrocytoma in 2018. After almost four years of intense treatments and operations, Samuel passed away in February 2022, aged 18.
