When I was diagnosed with epilepsy last November, Epilepsy Scotland became a real lifeline for me. The diagnosis and everything that meant and changed for me, was and continues to be a challenge to navigate. As many of those who live with epilepsy will say - it's about much more than seizures. It's the lack of control, the feeling of losing your freedom, the fear of stigma, and the side effects that come with living with the condition and medication. Throughout this time, I've been incredibly thankful to have the resources and support that Epilepsy Scotland have so readily available. The work they do to support those living with epilepsy in Scotland is invaluable. You can read more about my story specifically here: https://www.epilepsyscotland.org.uk/helplines-awareness-day-laurens-story/

"Epilepsy Scotland works with people living with epilepsy to ensure that their voice is heard. Around 58,000 people in Scotland live with epilepsy and we are here for anyone with this common serious neurological condition, their families, carers and employers.

We believe that people living with epilepsy have a right to be free from stigma and discrimination, have access to high quality medical, social, educational, support and information services be valued and included in society and determine their own way of life"