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Elle shares her experiences of being diagnosed with epilepsy, the impact the pandemic has had on her and how Epilepsy Scotland’s check-in service has helped.
Our Helpline & Information Officer, Stuart Macgee, provides five steps to combat the feelings of loneliness and isolation.
Our Policy Assistant, Anna Telfer, provides results of our COVID-19 has been affecting people with epilepsy survey and how important it is to consider the varied impacts of restrictions lifting.
Chris shares his experiences of how he felt after being diagnosed with epilepsy, what impact the pandemic has had on him and his advice to someone who has been newly diagnosed with epilepsy.
Our Helpline and Information Officer, Uschi Stickroth, looks at some of the facts every person with epilepsy looking for work should know.
The COVID-19 pandemic has seen many people unfortunately lose their job. Our Welfare Rights Officer, Tracey Millar provides some of the financial support you may be entitled to while looking for work.
Katie was diagnosed with epilepsy when she was just 14 years old. Here Katie shares how the COVID-19 pandemic has affected her wellbeing, mental health and how Epilepsy Scotland’s wellbeing service has helped her.
For National Epilepsy week, our Helpline and Information Officer, Uschi Stickroth, talks about post Covid anxiety.
Jan’s son Peter has been living with epilepsy since he was young child. Here Jan explains how she felt when he was diagnosed, how the COVID-19 has impacted on him getting the support he needs and the benefits that Jan has received from Epilepsy Scotland’s check-in service.
Epilepsy Specialist Nurse, Gareth Davison explains how the COVID-19 pandemic has affected epilepsy services in Scotland and what services will look like post pandemic.
Our Helpline & Information Officer, Stuart Macgee, provides information to help parents deal with their child’s diagnosis of epilepsy.
Our supporter Dan explains why he has signed up to our new RUN4SIX Challenge.
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