6 People You Meet Along Your Journey With Epilepsy
You’ve been diagnosed with epilepsy. A life-changing experience. Epilepsy doesn’t always show its cards and it can go unnoticed by family, friends and the public. With epilepsy being a part of your everyday life, you’re bound to meet a variety…
The Ultimate Gift Guide – Gift Ideas For Someone With Epilepsy
Epilepsy is hard to explain, let alone understand. It can be a real head scratcher to come up with an ideal gift for someone living with epilepsy, especially if you don’t live with it yourself. Not to worry! This gift…
Things To Never Do When Someone Tells You They Have Epilepsy
I remember the very first time that someone spoke the words, “Everything will be okay!” speaking about my epilepsy. Fire engulfed my stomach. When a family member spoke this to me, I knew they meant well, however, I wanted to…
Understanding Brain Fog And Epilepsy
Speaking candidly, alongside seizures, brain fog is one of the most difficult – and sometimes exhausting – parts of living with epilepsy. What does brain fog feel like? Brain fog is more than just the occasional forgetfulness. We all experience…
6 Ugly Sides of Epilepsy Most People Don’t Like Talking About
It’s no secret that having a chronic illness sucks. There are sides to having epilepsy that are ugly or not well studied, and many people don’t know about them at all. Yes, there are still myths – and I’m not…
The Road Doesn’t End Here
One of the most difficult challenges since my diagnosis with epilepsy is finding reliable means of transportation. Sure. I have my husband and members of family who extend their willingness to help me get to and from where I want…
How to Beat the Heat Living with Epilepsy
“‘Cause a little bit of summer is what the whole year is all about.” – John Mayer What do you think of when you hear the word “summer”? Vacation, flip-flops, the beach, napping all afternoon in the hammock, fresh squeezed…
What NOT To Do When Living With Epilepsy
Living with epilepsy, I often reflect on new and different ways to embrace the reality of my condition. Over the course of a decade, I’ve pursued and pocketed different suggestions for what to do, whether it be a new medication…
