We fight to improve the lives
of everyone affected by epilepsy


You have so many plans for the future and when they gradually start to fall apart you wonder if you can carry on.

I had my first seizure when I was 27. I'd started temping as an administrator and it happened at my desk. I've no recollection other than a paramedic saying my name and having excruciating pain where I'd bitten my tongue. I never went back to the office again, I was too embarrassed. I only went back to pick up my car, no one had told me I shouldn't drive. I actually carried on driving until I went to the Doctors a week later and the GP told me I should stop. This felt like the end of the world, but it was only the start.

A month later I began training for my dream career to become a police officer, but whilst on a placement I had another seizure, this time I fell backwards onto a stone floor and hit my head, I was taken to hospital as it needed stitches. Two seizures and a sleep deprived EEG showing the signs meant I was now diagnosed with epilepsy.

I was medically discharged from the police. I was at the lowest I could possibly be, the end of my career and no more driving until a year seizure free, I became depressed. Thankfully I had a supportive family and an amazing boyfriend who got me through the year.

I was eventually put on medication and for 7 years I was seizure free, it felt amazing! But then it happened again following a viral infection. It's happened once more since then when I was over tired. It's always at the back of your mind, if I have anything that feels like a aura or I'm feeling too tired I panic, but life has to go on.

For everything that has set me back eventually there's a positive. I got married to the boyfriend, have a daughter, started a career as a Broadcast Journalist and even jumped out of a plane (with a parachute). We don't always end up on the path we want, but maybe the ones we find on our journeys will be even better.

Keep moving forward.

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