Emily’s Perspective: Emily’s First Time Abroad
I recently traveled abroad with my sister. I was so excited, but as the day got closer, I became worried about all the ‘What ifs’.… Read More
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: 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™: 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
Epilepsy Blog Relay™: An Everyday Challenge
Emerging from the tunnel, I heard my mom’s voice say, “Jade, it’s okay now”. Living with Epilepsy is an everyday challenge.… Read More
Healthcare Debate: Leila’s Take on Managing the Cost of a Preexisting Condition
When I calculate the cost of each medication I take, I could be paying over $1000 per month to manage my epilepsy if I did not have insurance to help.… Read More
Healthcare Debate: Rachel’s Take on Living Without Healthcare Insurance
The future of healthcare in the United States has become frightening and scary for our family since three of my four family members have epilepsy.… Read More
Healthcare Debate: Abby’s Take on Living with a Preexisting Condition
Those working on the new healthcare bill that doesn’t cover preexisting conditions must NOT have any loved ones who are affected by one. … Read More