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Epilepsy Institute Categories: Your Stories

James White sharing his epilepsy story

Life with epilepsy: James’s story

Diagnosed at 25 after having his first seizure at work, James has had to learn more about his condition quickly and recognise the signs to keep himself safe. Although he’s faced many challenges, he has

Madeline at university in mortar board and gown

Life with epilepsy: Madeline’s story

Diagnosed at 13 after years of unexplained seizures, Madeline has faced complex investigations, brain surgery and the ongoing reality of drug-resistant epilepsy. She has written a book about her experiences and wants to help others

Laura and Alex smiling

Life with epilepsy: Laura’s story

Laura wants better representation of parents of children with additional needs in identifying key areas of research. She talks about her experiences of caring for her daughter with epilepsy and her hopes for the future.

A portrait of Ana

Life with epilepsy: Ana’s story

Ana says that epilepsy has affected every part of her journey through adulthood. It took her over a decade to get a diagnosis, so she wants to share her experience to help others in a

Edwina with her horse Willow

Life with epilepsy: Edwina’s story

Edwina tells of her experiences of living with epilepsy and how it has affected her mental health. She calls for more research to help those who live with both epilepsy and mental health issues.

Life with epilepsy: Maria’s story

Maria tells of her epilepsy journey with her daughter. They have had to go through many different medical professions suggesting different treatments, her daughter once endured 450 seizures in 24 hours and has a profound

Carly and her family with the Newcastle skyline behind them after doing the Great North Run

Life with epilepsy: Carly’s story

Carly and her husband Stu have completed the Great North Run 5 times, raising thousands of pounds for the Epilepsy Research Institute after research we had funded helped them to become parents, safely supporting her

Gracie smiling and hugging her sister Clara

Life with epilepsy: Gracie’s story

Many people don’t want to be defined by their epilepsy. They live life to the full. However, when SUDEP takes their life it comes as a massive shock to their friends and family. Here, Gracie

Life with epilepsy: Christophe’s story

For many families, navigating a diagnosis of epilepsy is a journey filled with uncertainty, hope, and resilience. Here, Christophe shares the emotional and medical journey of his son’s epilepsy, and his hopes for future research.

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