Tracking individual osteosarcoma cells to understand how they dodge chemotherapy
Dr Lucia Cottone at University College London hopes to understand how osteosarcoma cells become resistant to chemotherapy, which has a big impact on patient survival.
Dr Lucia Cottone at University College London hopes to understand how osteosarcoma cells become resistant to chemotherapy, which has a big impact on patient survival.
In this edition, we explore how each individual’s communication needs are unique – shaped by their personal experiences and preferred ways of sharing and receiving information.
The next Paediatric Oncology GRID Teaching Session will be on paediatric palliative care.
Constipation is a common symptom in children receiving palliative care.
April is Teenage and Young Adult Cancer Awareness Month (TYACAM) – an opportunity for charities and the young people we support to come together and raise awareness of the unique set of challenges facing this age group after being told they have cancer.
Ellie Philpotts was diagnosed with Hodgkin lymphoma in 2011 aged 15. She explains how she found support from other young people with cancer and how, through awareness raising, writing and advocacy work, she’s hoping to help those who are newly diagnosed.
Lisa Radcliffe’s son, George, was diagnosed with rhabdomyosarcoma when he was three years old and sadly died when he was four. Here, she explains how she and her husband, David, quickly found their own approach to communicating with George during his treatment, and how this helped them.
Multidisciplinary team (MDT) working is essential in children’s cancer care. Dr Ren Manias, Consultant Paediatric Oncologist at Southampton General Hospital and Contact’s medical adviser, explains how effective communication and shared decision making improve survival rates, enhance quality of life, and support children and their families during their cancer journey.
Becky Rodgers is a health play specialist at Sheffield Children’s Hospital. She tells us about her role in supporting children and young people (CYP) and their families during treatment, helping them to process information and express their thoughts and feelings.
Kate Hibberd’s daughter, Meredith, was diagnosed with b-cell lymphoblastic lymphoma in 2023 aged four. She tells us about how her family has navigated keeping people updated about Meredith's treatment, the importance of asking for support, and how connecting with other families of children with cancer helped them.