The ‘Epilepsy In Our Time’ films are available to view here
“Epilepsy is the most common serious brain disorder, affecting 6 million people in Europe, but is an under-recognised and poorly understood condition, often leaving individuals exposed to stigma and prejudice. We welcome any new initiative that raises awareness and understanding of epilepsy,” commented Mike Glynn, President of the International Bureau for Epilepsy (IBE).
“The Epilepsy In Our Time video diaries provide a candid insight into how it really feels to live with epilepsy, and a snapshot of society’s perceptions and understanding of this common brain condition.” concluded Mike Glynn The individuals filming their own lives for Epilepsy In Our Time come from a variety of backgrounds.
Lloyd, from the UK, traces his epilepsy back to a minor head injury following a car accident and has had to persevere in finding a treatment to control his seizures: “Finding a treatment that was suitable for my particular situation wasn’t easy, especially during the first few months after my diagnosis. Today, I see both my general practitioner and my neurologist for check-ups to make sure that my medications are still doing the best possible job for me,” Lloyd continued: “I’ve learned that epilepsy doesn’t have to be what others think – it’s what you make of it. Epilepsy is not something to be ashamed of - it’s like any other medical condition. Today, I think of my seizures as an unexpected guest at the front door. When someone shows up at your door without any warning, you have to see who’s there, but it doesn’t mean your entire life is interrupted.”
Monica, who lives in The Netherlands, did not have an accurate diagnosis or control of her epilepsy until the age of 45. “During my childhood, the clumsiness, the absent mindedness, the slight jerks in my arms - all signs of juvenile myoclonic epilepsy (JME) - went undiagnosed. That’s until I reached the age of 45. I was surprised to learn I’d been prescribed medications that weren’t suitable for JME and that my epilepsy had been misdiagnosed and therefore sub-optimally treated,” Monica continued: “I’d like to see everyone with epilepsy strive for the least amount of seizures and the least amount of side effects possible.”
Julie and David from the UK are parents to Dominic, an 11-year-old boy with severe epilepsy and learning difficulties. Julie said: “Dom’s learning disability means he can’t tell us how he feels when he has seizures. We can only imagine. These days, in a typical month, Dom has about 100 seizures. Dominic brings great joy to us, and on the good days I’m heartened by what might be possible in the future. His infectious smile and constant bravery seem to reaffirm my undying hope that one day we’ll be able to control this unrelenting condition.”
Marion, who lives in France, overcame her epilepsy in an extraordinary story to win an Olympic silver medal in cycling for France at the Sydney Olympics in 2000. “Epilepsy made me push myself. Eventually, with loads of hard training, I ended up making my way to the winner’s circle. Where there’s a will there’s a way. Today, as I look back on the titles and medals I’ve won, obviously I’m very pleased with my accomplishments, because I also won despite having epilepsy.” In the film, these five individuals discuss how they live with epilepsy day-to-day, and the ways in which they have sought to overcome challenges they have faced; their hopes and ambitions for the future; how they feel other people’s reactions to the condition have changed over time; as well as their personal pleas to the public about what they would like them to understand and know about epilepsy.
Epilepsy In Our Time is launched on the first European Epilepsy Day (14th February 2011) with the aim of improving understanding and ultimately, acceptance of epilepsy. It is hoped that these video diaries will challenge and dispel many commonly-held misconceptions about epilepsy, and help people to better understand the reality of living day-to-day with this condition. Epilepsy In Our Time will continue to follow the lives of Lloyd, Marion, Monica, David and Julie, making it possible for others to see how their experiences of living with epilepsy change over time, whether any of their hopes or ambitions are realised, and how they are treated by society as people living with epilepsy.
1. Epilepsy in the WHO European Region: Fostering Epilepsy Care in Europe
2. WHO. Epilepsy: aetiology, epidemiology and prognosis. Available at:
[Accessed 3rd February 2011]