Kelly Herriott’s daughter, Evie, was diagnosed with neuroblastoma in 2020 when she was 21 months old. Here, Kelly explains how Evie’s treatment affected her blood, offers advice to others facing a childhood cancer diagnosis, and tells us what life looks like for their family now.
Sian Brown’s son, George, was diagnosed with stage 4 neuroblastoma in April 2019 when seven months old. Here, she explains how she gave up work to care for George and the financial implications of this, and how volunteering work led her back into employment helping other families of children with cancer.
Mandy Berriman's son, Peter, was diagnosed with neuroblastoma in January 2019 when he was eight years old. She tells us how using social media to find information and connect with other families both helped her and presented challenges during Peter’s treatment.
Helen Pearson, Advanced Nurse Practitioner in solid tumours, researcher and CCLG member, explains how the findings of a study have helped co-design an important new web resource to support families.
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.
Single-cell transcriptomics linked to lineage tracing to interrogate the role of intra-tumour heterogeneity in shaping therapeutic susceptibility and resistance in paediatric cancer
Naomi Shefford-Thomas is CCLG’s Information Executive and mum to Phoebe, who was diagnosed with neuroblastoma in 2016. She tells us how invaluable online support from other parents helped her navigate her daughter’s treatment and offers advice to others looking to find the same.
Carrie Wright’s daughter, Lucy, was diagnosed with neuroblastoma in August 2018. She writes on participating in the international MiNivAN clinical trial and offers advice to others faced with making decisions about their child’s treatment.
Helen Pearson and Katie Johnson, co-chairs of the National Neuroblastoma Nursing Group (NNNG), tell us more about how they have developed a range of animation videos to help parents make decisions about their child’s treatment as part of a neuroblastoma clinical trial
