We have a variety of resources to support children and their families affected by hydrocephalus. These can be downloaded for free by children, their families and healthcare professionals. Please do not share or upload onto an external website without permission.
Download our resource tick list to tell us what information you would like. Please email this to the team info@harrys-hat.org so they can get the information ready for you. (If you represent a medical team, school or charity and would like multiple copies then please indicate the numbers and we do our best to provide subject to availability).
Hydrocephalus: What I wish I’d known is aimed at families affected by hydrocephalus, especially those who are just starting out on their journey. The 42 page book is packed full of parent stories, first-person hints and tips, as well as useful resources.
Hydrocephalus: Starting School is designed for families with children living with hydrocephalus. Inside, you’ll find advice and tips from other parents to help your child feel included, understood, and supported during their school journey. The 34 page book is packed full of parent stories, first-person hints and tips, as well as useful resources.
