Unrestricted funding lets us continue our core work supporting families affected by paediatric hydrocephalus and improving early diagnosis. As a user-led charity, our work is shaped by lived experience so funding goes where it has the greatest impact.
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Families affected by paediatric hydrocephalus often face delayed diagnosis, poor awareness and limited support. Parents are left anxious, under-informed and isolated while navigating complex medical decisions. Inconsistent understanding among professionals can lead to missed signs and late treatment, putting babies and children at serious risk.
Harry’s HAT supports families and improves outcomes through practical resources, family support, professional education and national awareness. We provide trusted information, comfort and sibling support, bring families together, and campaign for earlier diagnosis through better awareness of infant head circumference measurement.
