Hello everyone! I hope you all have been able to get some sort of rest and relaxation, and something fun in for yourself this summer! As my life continues to
I do not know anything different then life with Epilepsy, having been diagnosed at two years old. In recent years, I have been diagnosed with intractable epilepsy, which has me
Epilepsy comes in many forms/variants, and when I was in elementary school during the mid/late 1990s it was only the AOL internet days. So, it was a lot trickier going
Hello, my fellow Warriors, and caretaker warriors! I did something that I have never been able to do. I have been struggling with depression and anxiety for a while now,
Janice MacGregor's take on real Friends and epilepsy. Janice MacGregor is from Saskatchewan, Canada. She has had epilepsy with tonic clonic and absence seizures for eighteen years. Janice does
It’s crucial to address misunderstandings about epilepsy. That’s why this year’s virtual Purple Day® Around The World event shines a bright light on education. Although epilepsy is widely recognized,
Authors: Jim Merse & Lena Lache, Purple Day® Every Day Blog Editors Nearly 1000 people have registered for Purple Day® Every Day’s annual epilepsy education conference – learn more about
I think every person has the ability to look at their life as a series of “befores” and “afters”. In most cases, the befores and afters are moments to be
Author: Alyssa Holmes As we begin the journey of being diagnosed with epilepsy, it is difficult for everyone and different for all. When I say everyone, I mean everyone. That
Author: Maria Martinez Hey guys! I hope you all are doing great. I know during this time it can get stressful especially with us warriors. I was digging through some
