Epilepsy Blog Relay: One family pushing the boundaries of Lennox-Gastaut Syndrome
Lili was diagnosed with Lennox-Gastaut syndrome (LGS), a rare and severe form of epilepsy, but therapeutic horseback riding was an activity she could enjoy.… Read More
Lili was diagnosed with Lennox-Gastaut syndrome (LGS), a rare and severe form of epilepsy, but therapeutic horseback riding was an activity she could enjoy.… Read More
I never expected to be on this journey as an Epilepsy Mom but here I am.… Read More
Jes now writes Wishes for Mercy to inspire families battling epilepsy and to build supportive relationships within the special needs community.… 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.… Read More
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. … Read More
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. … Read More
Clair writes, Becoming a Mum with Epilepsy. She hopes women will be given the information & support to feel more confident and less alone in becoming a Mum… Read More