Epilepsy Blog Relay: New epilepsy diagnosis after seven years
After seven years of struggling to get a proper epilepsy diagnosis, Laura found a neurologist who would listen. She’s now a year seizure free!… Read More
Epilepsy Blog Relay: Coach gets honest about her epilepsy diagnosis
Despite fear and shame from stigma, this metabolic coach is ready to go public about her epilepsy diagnosis. Read how she found the strength to share her story.… Read More
Epilepsy Blog Relay: Help from an epilepsy support group
Early on, Soo’s family would not use the word epilepsy in their home. Now, she is an advocate and makes the most of her local epilepsy support group.… Read More
Epilepsy Blog Relay: Choosing hope despite brain tumor related epilepsy
Amber shares her story of brain surgery and brain tumor related epilepsy. She shares her struggle to find hope and create a life despite her challenges.… Read More
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