Epilepsy – My Invisible Disability
Edward shares, “For the past thirty-three years, I have been living with epilepsy, an invisible disability.”
My Journey with Epilepsy as a Young Adult: Keep Pushing and Stay Strong!
Brooke share her experience living with epilepsy as a young adult: I love to run, read, write, explore, take pictures and try new things.
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.
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.
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
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.
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.
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.