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Paediatric Epilepsy Research and Impact Report 2025
Young Epilepsy leads world-class childhood epilepsy research, delivering early diagnosis, precision treatments and better support for children and families.
Featured
Young Epilepsy leads world-class childhood epilepsy research, delivering early diagnosis, precision treatments and better support for children and families.
Featured
Children with epilepsy are at a greater risk of learning and behavioural difficulties than children without epilepsy. Despite this, there is a lack of research exploring the views and experiences of young people with epilepsy, their parents and school staff with regards to educational supports that could aid learning in children with the condition.
This document outlines the new, ongoing, and completed projects during July 2020 to June 2021.
An online survey was used to explore the perceived impact of COVID-19 and associated restrictions on young people with epilepsy in the UK
Young Epilepsy coordinates and funds research into the causes, treatments and impact of all aspects of childhood epilepsy. We want to secure the best outcome for everyone affected by the childhood epilepsies and we know the best way to do this is through research.
Young Epilepsy coordinates and funds research into the causes, treatments and impact of all aspects of childhood epilepsy. We want to secure the best outcome for everyone affected by the childhood epilepsies and we know the best way to do this is through research.
Young Epilepsy coordinates and funds research into the causes, treatments and impact of all aspects of childhood epilepsy. We want to secure the best outcome for everyone affected by the childhood epilepsies and we know the best way to do this is through research.
The objective of this study was to systematically review research that has focused on knowledge of and attitudes towards epilepsy among teachers.
Young Epilepsy coordinates and funds research into the causes, treatments and impact of all aspects of childhood epilepsy. We want to secure the best outcome for everyone affected by the childhood epilepsies and we know the best way to do this is through research.
The purpose of the SEEN study was to document, on a population basis, the development and behaviour of young children with epilepsy. The study also focused on emotional wellbeing, sleep and fatigue in their parents. A comparison group of children with neurodisability were included; these children did not have epilepsy but had other neurological or neurodevelopmental problems. This comparison allowed us to study whether having a child with epilepsy, specifically, has an impact on parental functioning.
The survey findings from our online survey of young people with epilepsy and their parents and carers to find out whether schools are providing support that complies with Government standards.
Young Epilepsy coordinates and funds research into the causes, treatments and impact of all aspects of childhood epilepsy. We want to secure the best outcome for everyone affected by the childhood epilepsies and we know the best way to do this is through research.