Ahead of International Epilepsy Day (Monday, 10 February 2020), Veera Parviainen from Finland shares her epilepsy story with us.
Elizabeth Dueweke is an epilepsy advocate and a winner of the IBE Golden Light Awards 2019.
Click here to read Elsa's story in English Érase una vez una niña con un cerebro…un cerebro como el de todos los demás. No le faltaba ningún detalle, era grande, rosa, retorcido y esponjoso. Era listo como el de los mejores científicos y fuerte como el de las guerreras más implacables. En aquel cerebro vivían
Click here to read Elsa's story in Spanish Once upon a time there was a girl with a brain ... a brain like everyone else's. No detail was lacking; it was large, pink, twisted and fluffy. It was as smart as the best scientists and as strong as the bravest warriors. In that brain lived
My parents told me that my birth on May 12, 2009 was difficult, and they called me Jad (an Arabic name meaning "generous" or "kind-hearted") because I was their best gift after marriage. They told me that I had a shock in my head in my first year childhood. When I was 18 months my
Once upon a time, there was a young woman who fell in love… They met in tango class. The girl was an university student, and the man was a doctor. They had long conversations. They imagined their future together. They wanted to have kids; one boy and one girl. But the woman had a very
My first EEG, in Boston ca.1966 — showed “clear”. My first MRI, in The Hague ca.1976 — showed “nothing significant”. All my EEG’s showed clear until my late 30’s. Even in 2015, when I was having seizures once a week, I reported at the Emergency Room with severe neurological symptoms (extreme trembling, intermittent vision loss,
I was not born epileptic. I got my first seizures in 2011 while in Basra, an oil port in southern Iraq. I was working in Basra as a baker. Initially, I did not take the seizures seriously. I ignored them for three months, thinking they would just go away. My roommate, a Ugandan, told me,
My name is Adel Bounif. I am 38 years old and live in the North East of France. I have a Master’s degree in Foreign Languages. I work in Luxembourg and am married. I have a daughter called Manel. She is 6 years old. She is suffering from Dravet syndrome. It is a rare genetic
A caring short film on Epilepsy Nina, The Little Bulldozer is a short film that is part documentary, part animation. Through the words of Nadia and Thomas Davies (Nina's parents) the little girl comes to life and symbolizes the spirit of overcoming. This unique short film was created by a world class group of extremely