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
For Father’s Day, this bride sends her Dad a note of thanks.… Read More
This post is part of the Epilepsy Blog Relay™, which will run from June 1 to June 30, 2018. Follow along! Getting real about constipation I’ve been on medication to manage my epilepsy for more than 30 years. On Living Well With Epilepsy we have talked about some of the side effects … 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