If your child has been diagnosed with neuroblastoma, our Family Support Team is here to provide emotional support, practical guidance and trusted information.

Learn more about neuroblastoma, including symptoms, diagnosis and treatment.

Find information about grants and other financial support to help with the financial impact of a neuroblastoma diagnosis.

An introduction to neuroblastoma from leading expert Dr Ro Bagatell, covering diagnosis, risk classification, treatment options, and current research.

Hear from parents and healthcare professionals about finding trusted neuroblastoma information and avoiding misinformation.

Exploring how families adapt to childhood cancer, with support, self-care, and peer connections.

An overview of current high-risk neuroblastoma treatment and key differences between COG and SIOPEN.

Practical advice from occupational therapist Joanna Hunt to help families understand and manage fatigue using the Spoonie method.

Understanding anxiety and post-traumatic stress in children and parents after childhood cancer.

Guidance on coping as a family and accessing support after a neuroblastoma diagnosis.

Understanding and addressing medical trauma in children and families, with practical strategies to support recovery.

Information about financial support, grants and helpful resources for families affected by neuroblastoma.

Learn about the different types of treatment for neuroblastoma.

A chance for families to learn from and connect with neuroblastoma experts.

Relaxed and inclusive events bringing together families affected by neuroblastoma for fun, connection and support.