Neill's story
Neill Lowdon is an artist from Cornwall who has recently sold 35 of his paintings to raise money for us. Here, he talks about leaving a legacy to Epilepsy Society in his will.
Georgina's story
My name is Georgina, I live in London and was diagnosed with epilepsy when I was 12 years old. I’ve worked in the film industry as a script supervisor for the past 6 years and love every minute of it.
Stuart's story
Stuart Watson, 39 from Howden in East Yorkshire, was so inspired by the support he received from our helpline that he decided to do a trek of the Great Glen Way in the Scottish Highlands and raise over £2500 for us.
Gina's story
Gina believes that her epilepsy helped her to embrace new career opportunities.
Jennie's story
Watch actress Jennie Jacques discussing the impact of her sister's epilepsy and what inspired her to fundraise and raise awareness of epilepsy.
Debbie's story
Debbie Jackson is currently feeling positive about her epilepsy. She is a personal assistant at a media company in Canary Wharf and feels supported by her boss and colleagues. People have been very good in understanding her condition when she has had a few seizures at work, but this has not always been the case.
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Mel's story
Mel talks about her experience from being first diagnosed with epilepsy, to becoming pregnant and seeking treatment and support from Epilepsy Society at our Sir William Gowers medical centre.
Epilepsy - it's not what you think
My name is Hayley and I'm a 36 year old secondary school teacher from Essex. I was diagnosed with Juvenile Myclonic Epilepsy about 20 years ago. I've been able to live a pretty normal life since my diagnosis which has included having two children, completing a degree and teaching qualifications.