Shareable Quotes from Epilepsy Blog Relay Stories
Here are a few great quotes from this month’s Epilepsy Blog Relay stories. Feel free to share these on social media. Each image links through to the full story.… Read More
Epilepsy – My Invisible Disability
Edward shares, “For the past thirty-three years, I have been living with epilepsy, an invisible disability.”… Read More
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.… Read More
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