Epilepsy Blog Relay: Chantal writes a letter to epilepsy
Chantal has been battling epilepsy for 19 years with the help of VNS. She shares a recent letter to her epilepsy.… Read More
Epilepsy Blog Relay: On life changing decisions and brain surgery
Karen on brain surgery for epilepsy: My life was going well, epilepsy didn’t stop me doing anything and I thought why take the chance?… Read More
Epilepsy Blog Relay: How the First Lady can influence disease stigma
As I began digging deeper into the history of disease stigma, I learned more about how the first lady has impacted stigma in a variety of disease states.… Read More
Epilepsy Blog Relay: On Rescue Medications for Epilepsy
Rescue medications for seizures and epilepsy have been on my mind a bit recently. Not because I’ve had seizures but because there’s been a few changes in my life that put me more at risk for seizures.… Read More
Epilepsy Blog Relay: On Epilepsy and Stigma
Okay so I’ll be honest the topic of epilepsy and stigma is a bit of a bugaboo of mine. But I promise to spare you the soapbox today and make it interactive.… Read More
Epilepsy Blog Relay: On the importance of questioning side effects
I now know I need to question all the potential side effects a medication causes, even the rare ones.… Read More
Epilepsy Blog Relay: On Epilepsy and Religion
Here we take a look at two different perspectives on the question of epilepsy and religion. On one side faith provided strength while on the other side faith meant losing a community of loved ones.… Read More
Epilepsy Blog Relay: Racing Toward Seizure Freedom
Former TV news anchor and marathon runner Sarah Carlson shares about her journey with epilepsy as she races toward seizure freedom.… Read More