Submitted by paige-dawkins on Mon, 05/03/2018 - 14:33
Princes to Kings are playing their first headline show in London for Epilepsy Society this Purple Day weekend. They were inspired to form their band by their eldest sibling, Luke, who has a severe form of epilepsy.
Submitted by paige-dawkins on Tue, 27/02/2018 - 15:59
Emma Friedmann is a parent carer of her 19 year old son who has fetal valproate syndrome. On the 21st February, she attended parliament when the government announced their decision to review handling of concerns around sodium valproate.
Submitted by paige-dawkins on Tue, 20/02/2018 - 13:03
Epilepsy Society's new Me and My Shadow scheme is launching to celebrate International Women's Day on 8th March.
Sign up & SAVE THE DAY for two epic fundraising events!
Submitted by paige-dawkins on Fri, 09/02/2018 - 10:35
Adam Franks describes how, with the help of his neurologist, he fulfilled his dream of becoming a professional ice hockey player, in spite of his epilepsy.
When seizures do not stop or one seizure follows another without the person recovering in between and this goes on for 30 minutes or more, it is called status epilepticus or ‘status’.
When we received a heartbreaking letter from ten-year-old Ellie, detailing the death of her friend Patrick from an epileptic seizure, we knew we had to share it with you.
A selection of the latest research papers from researchers at Epilepsy Society.
Submitted by helen-skipworth on Thu, 07/09/2017 - 16:13
Deborah and her two daughters all live with disabilities and all care for each other. Here she describes how they push forward together, never allowing epilepsy to beat them.
Submitted by helen-skipworth on Tue, 05/09/2017 - 16:43
Volunteers from the 'NCS Challenge' programme, a nationwide young person's volunteer initiative, rolled up their sleeves to help rejuvenate areas of Epilepsy Society's Chalfont Centre in Buckinghamshire.