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A new forum for epilepsy researchers

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Life with epilepsy: Janet & Emma

Janet and Emma discuss the impact of epilepsy and valproate on their families and what the Hughes report means for their campaign.
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Announcing theme leads for Enabling Technologies and Reproduction & Hormones research programmes

The Epilepsy Research Institute is pleased to announce the appointment of the theme leads who will drive the Institute’s research strategy for our ...
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International #EpilepsyDay: Why is international collaboration so important for research?

To celebrate International #EpilepsyDay, we caught up with Professor Andy Trevelyan to discuss the importance of collaborations across borders. And...
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Spotlight on… Dr Faye McLeod

In 2022, we were delighted to award Dr Faye McLeod  an Emerging Leader Fellowship to study the gene mutations behind rare epilepsies that develop i...
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The Hughes Report: why it’s important and why more research is still needed

Today, the Patient Safety Commissioner published The Hughes Report, with a series of redress recommendations for patients harmed by the anti-seizur...
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Patient Safety Commissioner publishes sodium valproate redress recommendations

Today, the Patient Safety Commissioner published The Hughes Report recommending redress options for those who have been harmed by the anti-seizure ...
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Epilepsy Research Institute welcomes new Chief Executive

The Epilepsy Research Institute is pleased to share the news that Rosemarie Pardington has now officially taken up post as our new Chief Executive....
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Epilepsy Research Institute hosts Roundtable with UK Dementia Research Institute

The Epilepsy Research Institute hosted a Research Roundtable with UK Dementia Research Institute this week at our head office in London. The event ...
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