Epilepsy Know

02/14/2026

With Tim Coles – I'm on a streak! I've earned a Emotions badge for 8 months in a row. 🎉

02/14/2026

With Deanna Cotten – I'm on a streak! I've been a top fan for 3 months in a row. 🎉

02/10/2026

With University Health Network – I'm on a streak! I've been a top fan for 3 months in a row. 🎉

02/08/2026

And here's a post that was on my FB page, and had to share this out. Please take care everyone.

https://www.facebook.com/share/1ahsuiF2GS/

02/08/2026

For people who live in Canada, I will be phoning the Canadian Epilepsy Alliance on Monday. This is to inform of the treatment I have received from not only my previous Landlord and his minion manager, but also from the Medicine Hat Regional Hospital and the Medicine Hat City Police. I've got a story about how I've been treated and the injuries I've suffered. So fed up of the ignorance that abounds out there.

02/05/2026

There are no word's, only tears to find out about the loss of a dear Friend from Fort McLeod Alberta. Her husband had text me saying that his wife Kathy Scout-Bastien had passed away in her sleep February 4th. She had a life-long battle with Epilepsy and no doubt passed away from SUDEP.
Kathy had been a very dear friend, and so I'm posting on my Epilepsy Know website. She was in her 50's and too young to die as we all are.
Deepest condolences to Kathy's husband Wade and their grown children. There are no word's.
Anyone who dares to think that Epilepsy isn't a challenge, look up SUDEP, as that's the diagnosis I had gotten before my surgery in 2019.
Having not heard of the term SUDEP, Specialists in the area of Neurology seem to be very uneasy broaching the subject.
So my beloved Kathy, you've earned your wings to a more joyous ending. It won't stop my tears for a while. R.I.P my dear.

02/02/2026

Sharing this out, as SUDEP is definitely not a diagnosis you want to be diagnosed with. Onward and Forward us Epilepsy Warrior's must go, to spread the word on Epilepsy and the many different types of Epilepsy. Wishing everyone a great day out there. Huggs to all.

Purple Day is on the horizon on 26th March 2026.

Last year, so many of you helped make our Purple Day campaign a success, raising vital funds and awareness of epilepsy. Whether you’ve joined us before or are new to our community, we’d love you to get involved this year and help make an even bigger impact.

Save the date and keep your eyes peeled for more information!

02/02/2026

With James Williams – I just got recognized as one of their top fans! 🎉

02/02/2026

Sharing this out there to inform others about your group and website that you're working on. All the best to you and everyone out there affected by Epilepsy. All the best going forward.

Hoping your 2026 is off to a great start! This year Purple Peace is looking forward to new opportunities for education, community involvement, and breaking down stigmas around epilepsy. We hope you will join us this year on this journey!

02/02/2026

With Nature Science – I'm on a streak! I've been a top fan for 3 months in a row. 🎉

02/02/2026

With Tim Coles – I'm on a streak! I've earned a Emotions badge for 7 months in a row. 🎉 Keep going forward Tim, one day at a time.