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
This post is part of the Epilepsy Blog Relay™, which will run from June 1 to June 30, 2018. Follow along! Sharon’s Story Sharon Ross has a rare type of epilepsy. Though she has experienced seizures, the main impact the condition has on her life is her cognition. According to Sharon, her … Read More
This post is part of the Epilepsy Blog Relay™, which will run from June 1 to June 30, 2018. Follow along! Brodi’s Story Epilepsy should be a four-letter word, or so I thought. I have lived with epilepsy since I was three years old, and while my episodes have certainly frustrated and … 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