Just last week, hundreds of people living with epilepsy and their supporters came together to raise…
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It’s been a few months since my last blog. First, I want to sincerely thank the…
This poem sums up how I feel. Now I lay me down to sleep don’t let…
Okay y’all, I’m just going to say it. This one is not going to be easy…
“Thank you so much, this brought many smiles to our team let alone to the patients…
It was 1993, and I was a 21 year-old senior at Duke University double majoring in…
Hello everyone! I hope you all have been able to get some sort of rest and…
I do not know anything different then life with Epilepsy, having been diagnosed at two years…
Epilepsy comes in many forms/variants, and when I was in elementary school during the mid/late 1990s…
Hello, my fellow Warriors, and caretaker warriors! I did something that I have never been able…
Janice MacGregor’s take on real Friends and epilepsy. Janice MacGregor is from Saskatchewan, Canada. She…
It’s crucial to address misunderstandings about epilepsy. That’s why this year’s virtual Purple Day® Around…