Epilepsy Blog UK, Epilepsy in Childhood

There are around 112,000 children and young people in the UK living with epilepsy, often linked with other neurological conditions. Throughout November on the Research Blog, we looked at how early diagnosis and genetic screening can lead to improved treatments and reduce the impact of epilepsy on young people’s lives.

In our final Research Roundtable webinar of the year, our fantastic blog contributors from the month, Hannah, Dr Tim Tierney, and Dr Joseph Symonds joined us to discuss their experiences and research into childhood epilepsy. Don’t worry if you missed it – you can watch the full session here.

To be the first to hear about these sessions and get the chance to register for events, please sign up for our mailing list here.

Watch our Research Roundtable on Epilepsy in Childhood

Promoting, encouraging and funding research into the causes, diagnosis and clinical management of people with epilepsy and associated conditions

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Developing the next generation of epilepsy researchers and capacity building the epilepsy research environment with our new Doctoral Training Centres

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Accelerating innovations for people with epilepsy by supporting research that will influence clinical practice and health policy

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