Epilepsy Blog Relay™: Interview with researcher Sarah Collard
I recently had the opportunity to interview Sarah Collard, a Fellow at Bournemouth University following the release of her article on Epilepsy & Exercise.… Read More
Epilepsy Blog Relay: Participate in Twitter Chat on Healthcare and Epilepsy
We close every Epilepsy Blog Relay™, with a live twitter chat. Today we share instructions, & questions to guide our discussion on healthcare and epilepsy.… Read More
Emily on Living with Absence Seizures
Emily has a positive outlook regarding epilepsy and despite living with absence seizures she has become an outspoken advocate sharing hope with others.… Read More
Epilepsy Blog Relay™: Leila’s Epilepsy Resolution Update
In January, I made a few Epilepsy Resolutions. I wanted to re-energize myself and do a better job at managing my epilepsy. I promised to keep you updated on how I’m doing…it’s not pretty, but here’s my first self-evaluation.… Read More
My Epilepsy Doesn’t Just Affect Me
Jessica’s Story: I didn’t really start Living Well With Epilepsy to tell my own story. But fair is fair, I suppose it is time to share my story.… Read More
Epilepsy Blog Relay: When Giving Up Is Not An Option
When I was diagnosed with Epilepsy at the age of six, my life transformed into a monsoon. I started having trouble socially, academically, and physically. It seemed as if my world was in a downward spiral until I was introduced to softball. That is where I learned that giving up was never an option.… Read More
Epilepsy Blog Relay™: Soo’s Story
Soo writes the blog Soo’s Epilepsy Corner. Soo is living with epilepsy and has dedicated her efforts to raising epilepsy awareness.… Read More
Epilepsy Blog Relay™: A Mom’s Perspective
This post is part of the Epilepsy Blog Relay™ which will run from June 1 to June 30, 2017. Follow along! For the blog relay this month, I wanted to provide another perspective. By now, you know mine. Epilepsy sucks. It’s a challenge… all. the. time. But, I always try to remember … Read More