TONIC: Series
TONIC - Season 1
Borrowing from the cinematic genre, the 8 episodes of the mini-series TONIC present the journey of a young woman
22-year-old woman coping with epilepsy in different
situations in her life. We observe the repercussions of her condition in different contexts. We see a different obstacle in each episode, which helps us better understand what it's like to live with epilepsy. Through this series, a dose of hope is spread, enabling young people
young people living with the neurological disorder to
identify with the character and see the positives in their lives, despite the constant struggle.
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TONIC: Podcast
TONIC - The podcast
The podcast is a series of interviews linked to each episode of the TONIC web series. The podcast is hosted by Èva Perreault-Gagnon, director of the TONIC web series, with the participation of Anie Roy, director and counsellor at Épilepsie Montérégie. Our guests include people living with epilepsy, as well as those involved in the world of epilepsy.
Join us as we demystify epilepsy in a series of heartwarming interviews.
Season 1 now available!
On that note, welcome to the UNIVERSE OF EPILEPSY...
Distribution platforms
Are you ready to learn more about epilepsy? We have a lot to share with you to demystify demystify and help understand this condition.
Embark on this adventure with us through a series of meetings.
To listen, here are the links:
and available on other free applications too.
It's a start!
-Èva, your animatrice✌️
TONIC
The refill kit
The Recharging Kit is for you if you're living with epilepsy and making the transition to adulthood. We hope this kit will help you get through this period in optimum condition.
SECONDARY
This kit is for you if you're a teenager living with epilepsy and attending high school. With this kit, we want to offer you a little peace of mind and contribute to your well-being in high school.
CEGEP AND UNIVERSITY
This kit is for you if you live with epilepsy and frequent the CÉGEP, university or other post-secondary studies. In this document, you'll find information and ideas for teamwork with teachers and other students.
Epilepsy #52
Epilepsy doesn't come in just one form, as stereotypes may proclaim. For some, like me, it's completely invisible. Many of my friends were unaware of my diagnosis over 10 years ago. Having this disease doesn't define me. But it does force me to face challenges every day. The best way to support people like me is to educate yourself and those around you. This allows society to adjust to us instead of the other way around.
I hope this short 6-minute film will help you understand and feel how I live with this condition.
Want to experience it from my perspective?
This short film is for you!
Welcome to my shoes 🙂
-Signed, Èva
English 
French