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Our fantastic volunteer, Dave McTernan shares why he volunteers for Epilepsy Scotland and what he has gained by volunteering. My role as moderator in the Facebook support group is to help with the smooth running of the group. To add new members when requested and to ensure that it’s a safe and confidential environment by …
We spoke with 17-year-old Ailsa about her experiences of epilepsy, school and deciding to continue her studies. Ailsa just finished high school and is going to university to study music. When were you diagnosed with epilepsy? I was diagnosed with epilepsy when I was 11 or 12, in my second year of high school. …
Nicole has been living with epilepsy since December 2014. Here she shares how she felt when first diagnosed, the impact epilepsy has had on her life and what she would say to others who have been recently diagnosed with epilepsy. How did you feel when you were first diagnosed with epilepsy? I was in …
Our Communications Officer, David Coates, looks at five frequently asked questions about epilepsy that we receive via our freephone helpline. It’s never easy being given a diagnosis of epilepsy. Like everything else, you will need time to process the information. You may also have lots of questions about epilepsy and what your new diagnosis means …
We are thrilled be launching this year’s #StudentSeptember Campaign. Throughout the month of September, we will be campaigning to increase awareness of epilepsy in further and higher education. Our Student Campaign We are campaigning to ensure there is dedicated support available for students with epilepsy during their time in college or university and to …
Lesley was diagnosed with epilepsy when she was 16 years old and has been living with epilepsy for 49 years. She shares her story and the challenges she has faced. I was born in the UK but lived in Zimbabwe for over 46 years, where I had a good education and was a champion swimmer …
Our Communications Officer, David Coates, looks at five ways to help manage your child’s epilepsy and seizures. Most children are initially more concerned about the impact epilepsy may have on their life when first diagnosed. Provide reassurance and answer any of their questions as much as you can. Staying positive around your child can make …
Claire was diagnosed with epilepsy four years ago. She shares her feelings when first diagnosed and the challenges she faced and how she has overcome them. How did you feel when you first knew you had epilepsy? When I was first diagnosed with epilepsy in July 2018, I was completely stunned. I’d been having …
Our communication officer David updates us on the latest government announcement for the COVID-19 autumn booster. We have already received some enquiries about the autumn booster for people with epilepsy. The good news is that people with epilepsy yet again are included in the at risk group. This makes them eligible for the autumn booster. …
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