Epilepsy Blog Relay™: Spreading the word with Thunderclap
Living Well With Epilepsy has created our very own using Thunderclap to spread the word about the Epilepsy Blog Relay™.… Read More
Epilepsy Blog Relay™: Silver lining playbook
Ever woken up to find three beautiful, strong men smiling down at you? Handsome paramedics (and EMTs) are truly the silver lining to seizures. … Read More
Epilepsy Blog Relay™: Jenny LaBaw on Epilepsy and Fitness
As a fitness professional, I encourage other people living with epilepsy (and their families) to focus on their health. This means sleeping well, keeping stress low, eating healthy and keeping active. … Read More
Epilepsy Blog Relay™: Staying strong no matter what
As a baseball player having so many seizures (over 40-50) and being put on all sorts of medication impacts performance. So staying strong mentally and physically is really important to me.… Read More
Leila’s Ideas: Speaking about stigma at the Mardi Gras Gala
Sometimes, in my fight to eliminate stigma and live a “normal” life, I create the perception that my life is easy and free from struggle. However, in my speech at the Epilepsy Foundation of Western/Central Pennsylvania’s (EFWCP) annual Mardi Gras Gala I showed what life with epilepsy is like–both the good and the bad parts.… Read More
Emily’s Perspective: Young Epilepsy Champions 2016
Young Epilepsy Champions Awards will celebrate the achievements of children and young people with epilepsy.… Read More
Thinking about epilepsy camp?
Have you been thinking about participating in a local epilepsy camp? Here you will find info on a few camps around the country. … Read More
Megan’s Story: Have you heard of vertiginous epilepsy?
My name is Megan and I have a very rare type of epilepsy known as vertiginous epilepsy, or commonly known as epileptic vertigo. … Read More