Appreciating the small things and embracing every opportunity
Sarah Dransfield was diagnosed with bone cancer in March 2012 aged 16. Here, she tells us what helped her during and after treatment and how cancer has changed her outlook on life.
Sarah Dransfield was diagnosed with bone cancer in March 2012 aged 16. Here, she tells us what helped her during and after treatment and how cancer has changed her outlook on life.
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.
Charlotte Hillyard’s daughter, Jess, was diagnosed with a brain tumour in May 2023 aged three. Knowing the importance of peer-to-peer support, Charlotte and her husband, Lee, set up Walking Warriors Essex earlier this year to bring together families of children with cancer to share their feelings and experiences.
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.
Skin cancer (melanoma) in teenagers and young adults (TYA) is on the increase and evidence from young people and their families suggest that they feel isolated, alone and unsupported.
Claire Bailey's daughter, Poppy, was diagnosed with stage 4 high-risk neuroblastoma in July 2020 aged four. She writes on how the relationships she’s formed with other families have provided support both during and after Poppy’s treatment.
The Ellen MacArthur Cancer Trust (EMCT) takes young people aged eight to 24 years old on free sailing and outdoor adventures to help rebuild their confidence after cancer. Scott Wilson, of the Trust’s communications team, and Rebecca and Simran, two of the young people it’s supported, describe how the trips help bring people with similar experiences together and why that’s important.
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.
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.