Epilepsy Canada
600-3250 Bloor St. West, East Tower M8X2X9 Toronto, ON, Canada

Meet Marika, one of our brave #FacesOfEpilepsy. Marika was diagnosed when she was 3 years old. She’s faced stigma and hard experiences with first responders. This has lead her to become a vocal advocate for Epilepsy Awareness! To read Marika’s story check out the link in our bio.

Thank you to everyone who participated in Epilepsy Awareness Month. We were so moved to see so many of you using your voices, bravely sharing your stories, building awareness, teaching epilepsy first aid, dispelling myths, fundraising, and donating. All of your actions make an incredible impact. And we are so grateful. Together, we will continue to work to fund research and find a cure!

As we come to the end of Epilepsy Awareness Month, we’re so touched by the incredible action we saw people taking across the country! Thank you for tagging us in your all your posts and showing us your purple!

Epilepsy doesn’t care about your age.

Our Partner Organization @cureepilepsy is hosting a free webinar next Tuesday April 13th on the topic: Siblings and Severe Childhood Epilepsy: The Impact of Seizures on the Family’s Mental Health This webinar is free to attend. Viewers can ask questions during the live Q&A or submit questions in advance via [email protected] To register: https://www.cureepilepsy.org//siblings-and-severe-childho/

Our last Take Action Tuesday of Epilepsy Awareness Month. And the action is donate. We are asking you to donate to the important research we are funding that is saving the lives of people living with epilepsy. Research takes time, and it’s incredibly expensive, says Gary Collins, President of Epilepsy Canada. So in order to improve the lives of people living with epilepsy, we need time and money.... Any gift, no matter the amount, is so important and so appreciated. Thank you for considering to give. To donate follow the link in our bio.

Having a seizures does not always mean you have epilepsy. They can also happen because of other medical problems. These problems can possibly include: A high fever, low blood sugar, alcohol or drug withdrawal.

Meet 7-year old Marylee, one of our brave #FacesOfEpilepsy. Mary was diagnosed with epilepsy when she was three years old. Her parents are determined to not let Mary’s condition rule her life. Before COVID hit, she was taking ballet lessons during the school year and soccer in the summer. She took swimming lessons as well. Now, she wants to play drums and practice figure skating. She loves cooking and baking, and she is a great artist! To read Marylee’s story visit our website: https://www.epilepsy.ca/stories/marylees-story

Meet Joel, one of our brave #FacesOfEpilepsy. Joel, talks about how he has not epilepsy stop him or hold him back from doing what he loves snowboarding! To read Joel’s story about having a positive mindset, check out the link in our bio. And to donate to help research to find a cure check out the link in our bio

Thank you again to everyone who shared photos and tagged us in your inspiring pictures

Mark your calendar for the 3rd annual epilepsy awareness concert Unshakeable"! On Monday February 8th the virtual livestream concert will be available to watch via Facebook or YouTube Live, raising monies for Epilepsy Research with Epilepsy Canada. While the concert is free to watch, viewers are encouraged to donate. ... Unshakeable features singers and instrumentalists from across Canada who have come together to share their talents in support of epilepsy awareness. These musicians will perform in a variety of styles everything from jazz to classical, opera to musical theatre, and pop to folk and all musical collaboration is either within Covid bubbles (musical families and couples) or through the magic of technology. This year’s concert also includes a virtual ensemble number of over 90 singers from BC to the Maritimes! For more details on where to watch and how to donate, follow the link in our bio

The latest news for you from Epilepsy Canada

A rock star supporter, Maya, wrote to us to share how she's learning, teaching others, and making positive change for epilepsy - all from her classroom! Check out how she's making her mark for epilepsy in her letter below. Thank you Maya!

Did you know that Dravet Syndrome is a rare form of epilepsy that begins in infancy and leads to frequent and severe seizures? Today is International Dravet Syndrome Awareness Day. The day aims to raise awareness for and create a better public understanding of the syndrome. ... #epilepsyawareness

Vanessa has used the past few months to slow down, recover, and focus on new projects. What habits have you picked up during social distancing? Let us know below and read on for her full story: "When we first went into quarantine, unfortunately I had a seizure and didn’t make it to my 2 year seizure free mark. It was a very hard time for me. Especially since I couldn’t have my fiancé there with me at the hospital. I immediately wanted to get out of there and go home as soon a...s possible because who wants to be in a hospital when there is a virus going around? During this time I was stressed, my job came to a halt, it was uncertain when I could travel to see my family next, etc. But, I’ve also learned to stop and be thankful for so much in my life. Maybe this was a sign from my body to slow down, take a break, recover, stop stressing. I tried to look at the positives. I’ve been keeping busy by building and creating a small business that I have dreamed of for a while. It’s a work in progress, but I’m grateful for this time to help me get started. I can proudly say that I am *almost* (knock on wood) 3 months seizure free. I hope everyone is staying safe & healthy during this time and can look at the bright side. We’re in this together!" #epilepsyawareness

The search for a cure continues. We're committed to funding the vital research we need to #endepilepsy. Curious to know what projects our donor dollars are powering? Check out our 2019 research report here: https://www.epilepsy.ca/2019-research-report.html

We want to thank the people, organizations, and Champions that have continually supported Epilepsy Canada. Each of our ongoing donors has made a meaningful difference in the lives of those living with epilepsy across the country. Their generous contributions and fundraising efforts have helped us fund vital research that will lead the way for an eventual cure. We invite you to visit our Honour Roll and help us celebrate Epilepsy Canada's ongoing supporters: https://www.epilepsy.ca/honour-roll.html