The good bad and ugly of epilepsy online support communities
Hayley shares her experience with epilepsy online support communities for those newly diagnosed, or just new to online support.… Read More
On explaining epilepsy to peers
Being an individual living with epilepsy, the one question I get a lot is, “What is epilepsy?” The scientific definition is a chronic neurologic disorder with many possible causes including illness, brain damage, or abnormal brain development.… Read More
When embracing cowardice shows bravery
Just because I appear brave doesn’t mean that I’m not hiding a coward inside that I’m now prepared to admit and take responsibility for… Read More
When hope returns to a life with epilepsy
A little bit of hope has returned and grows every week, every month, like a light at the end of a long, dark tunnel as I continue parenting with epilepsy.… Read More
Why was the June Epilepsy Blog Relay Delayed Until July?
I am planning to run the Epilepsy Blog Relay this July to fulfill the promise I made to you and to myself. I hope you will follow along.… Read More
When a Husband Becomes Epilepsy Caregiver
My husband, Pete, and I met before my diagnosis. But, when I was diagnosed with Intractable Seizures, Pete became my life-line.… Read More
COVID and our Epilepsy Superheroes
As our world has dealt with the reality of being confined to home due to COVID – many of us felt the pressure in unique ways. But perhaps those of us with epilepsy also found some freedom.… Read More
Emily’s Perspective: Newly diagnosed with epilepsy or epileptic seizures?
Are you new to Epilepsy? Have you had a recent diagnosis of epileptic seizures in your family? Maybe I can help ease the anxiety with this column.… Read More