news

The Department of Transport wants to hear from people with epilepsy and other disabilities about their experiences of travelling on public transport.

People with epilepsy could benefit from new guidelines announced by the Government this week, for assessing those who receive PIP - the Personal Independence Payment...

A standing ovation as Epilepsy Society's Professor Philip Patsalos is awarded the 2016 Excellence in Epilepsy Award by the British Chapter of the International League...

Although we could not see them as we watched today's  sodium valproate debate  via Parliament Live TV, the presence of three women -Janet Williams, Emma Murphy and...

Epilepsy Society's chief executive, Clare Pelham, has welcomed a second letter from the Department of Health in response to her letter to health secretary Jeremy Hunt...

Arlene Foster, leader of the Democratic Unionist Party and First Minister of Northern Ireland has pledged her support for Epilepsy Society's campaign to ensure...

Epilepsy Society's chief executive, Clare Pelham, receives a response from health secretry Jeremy Hunt about safety issues around epilepsy drug, sodium valproate.

This Thursday (19 October 2017), MPs will be meeting  in the House of Commons to debate safety issues around the epilepsy drug sodium valproate.

Following last month's public hearing into the epilepsy drug sodium valproate, the European Medicines Agency(EMA) has now published a full summary report.

Teva lamotrigine dispersible drugs are currently unavailable in 5mg, 25mg and 100mg strengths. This is due to problems with the manufacture of the drug.