In May of 2025, I had my first seizure. I ended up having two seizures back-to-back, and because they happened so close together, doctors initially considered it a one-off experience. Three months later, to the day, I had another two seizures. This time, I was officially diagnosed with epilepsy. Since then, I have had four more seizures, with my most recent occurring in May of 2026. The past year has been a rollercoaster, not just for myself, but for my family and friends as well. I have had numerous tests and appointments, filled with questions and uncertainties. My EEGs and MRI have all come back clear, there has been no known source or cause for my seizures. While there is still a lot that I don’t know about my epilepsy, one thing I do know is how fortunate I am to have the people around me. My family and friends have made countless sacrifices to make sure I’m safe, supported, and able to continue living my life as normally as possible. I will always be grateful for that. I also know that my experience with epilepsy is different from someone else’s. There are so many people living with this condition who face challenges every single day. Whether that’s frequent seizures, constant medical appointments, medication changes, or simply trying to navigate a life that can change without warning. That’s why I’m taking on Epilepsy Canada’s 1in100 Challenge. I am doing this for everyone living with epilepsy, for the families and friends who support them, and for the people working toward a future where epilepsy is better understood, better treated, and ultimately easier to live with. If you’ve supported me in any form through this past year, I want you to know how much it has meant to me. And if you’re able to support my 1in100 Challenge, whether through a donation or simply by sharing my page, it would mean a lot to me. Thank you to everyone in my life that has been there for me, and thank you to Epilepsy Canada for funding and supporting further research into this condition everyday.