On CDKL5: A story of a hard to recognize illness in kids
According to Randi, “When our daughter first had a seizure it was subtle, quick, and questionable.” Today, she shares a story of hard to recognize seizures.… Read More
Traveling with Epilepsy: Finding Adventure in Slovenia
Sometimes, finding adventure means ignoring fears and jumping in with both feet. Going canyoning in Slovenia required just that!… Read More
Reimagining The Third Door Following an Epilepsy Diagnosis
Landis shares how her epilepsy diagnosis caused her to reimagine Alex Banayan’s concept of The Third Door.… Read More
5 tips for dealing with an epilepsy diagnosis
Many of us will face a devastating diagnosis and some will even face life with a chronic illness, like Epilepsy. Here are a few tips to help.… Read More
Adjusting to an Epilepsy Diagnosis
Kristine shares her experience with adjusting to an Epilepsy Diagnosis. She describes her fears, denial and experience of feeling isolated.… Read More
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