Adults with epilepsy in social care could be on wrong medication
Researchers at the Epilepsy Society fear that adults in social care with epilepsy and learning disabilities could be receiving the wrong medication or treatment due to a lack of diagnosis.
Epilepsy Society shortlisted for top award
All of us at the Epilepsy Society are delighted to have been shortlisted for a prestigious campaigning award.
Why MP Sarah Green is changing her name to Sarah Purple
It could be something to do with her name, but MP Sarah Green has a propensity for changing the colour of the landscape.
Zach’s Law not in first reading of Online Safety Bill but the campaign continues
The Epilepsy Society is disappointed that Zach’s Law was not included in the first reading of the Online Safety Bill in Parliament yesterday. However, we are hopeful that the new offence to protect people with epilepsy from internet trolls will be included at a later stage in the legislative process.
MPs say draft online safety laws not "clear or robust"
MPs who have been supportive of Zach's Law argue that there is still more to do in tightening the draft online safety laws.
Helping to shape the future of research
What matters most to you about epilepsy research? What are the outcomes that are most important to you? If you could sit down with a researcher, what would be the top three priorities that you would like to them to focus on in their epilepsy research?