~Epilepsy in Real Life~
We were with three other couples, and randomly enough, one of the couples knows someone with epilepsy, another couple (us) has epilepsy, and a third couple's child is currently testing for newly emerging epilepsy… 3 out of the 4 couples somehow touched by Epilepsy. And that's not why we were together... the conversation unexpectedly ended up there.... Continue Reading →
Maybe you’re new to Epilepsy and in that case, one of my usual posts depicting daily life or the continual struggles/side effects would be most helpful. However, today is short and sweet for once. I welcome the newbies but I’m talking to the “old timers,” whether Epileptic yourself or a caregiver...
The goal is to establish care for all seeking answers for his/her Epilepsy and begin to provide more hope for the families fighting this disease together. With less than 15 epilepsy specific neurosurgeons nation-wide, with only 2 using specific cutting-edge robotic devices on the West coast, we are starting here...
Twenty years ago, I didn't take the chance to be my own advocate, but now I have the chance to understand what's out there... and not be afraid of it...
(This post is part of the Epilepsy Blog Relay™ which runs from November 1 through November 30.) You know what a new med is like? It's like hope, optimism, your savior, terror, your enemy, the one thing that can make you worse. This last time, while I was in the hospital, we ditched one med... Continue Reading →
In Megan's Shoes 