Carley’s Story: Living with Epilepsy
I am Carley Jones and I have been living with epilepsy since I was 13 years old. … Read More
Emily’s Perspective: Home Treatment
This month I am going to be focusing on home treatment for Epilepsy. There are a few things you can do to make things a little less stressful or tiring.… Read More
Traveling with Epilepsy: A Pharmacy in Croatia
My husband and I decided to do a weekend getaway to Zadar, Croatia. Part of going on vacation with epilepsy is doing the pill count thing. … Read More
Epilepsy Blog Relay™: Seeing Seizures from a New Perspective
Though I’ve lived with Epilepsy for most of my life, watching a family member experience seizures for the first time was harder than I ever imagined.… Read More
Epilepsy Blog Relay™: Epilepsy, depression and a little creativity
This post is part of the Epilepsy Blog Relay™ which will run from November 1 through November 30. Follow along and add comments to posts that inspire you! Having a medical condition is difficult, some individuals deal with their condition better than others, but the struggle is generally still there. Many people find … Read More
Emily’s Perspective: Parenting with Epilepsy
Many people living with Epilepsy are also parents. In this article, I offer suggestions for parenting while managing Epilepsy.… Read More
Leila’s Ideas: Balancing Life and Epilepsy
Trying to live a “normal” life while managing Epilepsy can be difficult. How are you balancing life and epilepsy?… Read More
Emily’s Perspective: Thoughts on the show “Epilepsy & Me”
Living with Epilepsy It’s scary, living in fear, living the unknown, not knowing when your next seizure will strike, if it’ll strike again at all. That’s what it’s like, living with an invisible disability. It’s hidden and sometimes, without warning, it can strike. I’ve lived the last 11 years of my life … Read More