Epilepsy Blog Relay: Building supportive relationships within the special needs community
Jes now writes Wishes for Mercy to inspire families battling epilepsy and to build supportive relationships within the special needs community.
Jes now writes Wishes for Mercy to inspire families battling epilepsy and to build supportive relationships within the special needs community.
For Father’s Day, this bride sends her Dad a note of thanks.
Reflecting on my life with epilepsy, I remember the medications and how they made me feel, the hospital stays, and the many, many doctor appointments. This Mother’s Day, it’s time for a special thanks to my mom who was there through it all. Looking back on the early days When I … Read More
A passion for creativity was something I hoped to pass on to Colleen. From a child to adult, I have always had a love for drawing, music, paint…anything in which I could create something of my own.
This post was written by Darla Davison, mom to Aaron who has Lennox-Gastaut Syndrome (LGS), a rare and severe type of epilepsy. Living Well With Epilepsy is grateful to Lundbeck, Champion Sponsor of the March 2018 Epilepsy Blog Relay™. Thrilling, Inspiring, Better together “This photo was taken just a day or two … Read More
Jes Armstrong is back again to share an update from her blog Wishes for Mercy, a blog about her experiences as mother to a special needs child who looks normal at first glance.
Sara’s Story: Getting around without a car (with kids!)
If someone had told me a year ago that in 12 months we would be doing most of our daily traveling by electric bike, I would have laughed. I live in Portland, and have a 3-year-old and a 5-year-old. It rains here for about 5 months out of the year. But, it happened.
From Dave: My son wakes up every day and takes a handful of pills. He may have already had a few seizures and he has to will himself to get ready for school.