We feature guest bloggers who share their insight on living with epilepsy.
Watch Olivia’s first video blog where she shares her experiences of starting university.
Jenny, who currently works at Young Epilepsy, talks about her experience living with epilepsy.
You can read Nikki's blog Slugs and Snails Tales where she shares her experiences on living with a child who has epilepsy.
Guest blogger Emily speaks about how to keep safe in the summer holidays.
Katie shares her inspirational cycling journey and her tips on staying safe whilst riding.
Yasmin talks about how she is finding transitioning from university into the world of work
International Day of People with Disability Today, Saturday 3 December, marks International Day of People with Disability (IDPwD), which aims to increase awareness, understanding, acceptance and celebrate the achievements of people living with a disability.
James Gaydon is the Challenge and Sports Events Manager at Young Epilepsy, here he shares a blog he wrote about his experience of being diagnosed with epilepsy, his feelings at that time and how he has triumphed over his condition. Getting my head around it
Epilepsy impacts on every part of your life, I think potentially that’s one of the hardest things to accept when you are diagnosed - it affects everything. It affects your ability to drive, the jobs you can do, how you learn at school/university, your social life and the most private aspect of your life…relationships.