Epilepsy Blog Relay: Tips to feel less isolated and alone after an epilepsy diagnosis
Michael shares how he feels isolated and alone since his diagnosis of epilepsy. He doesn’t know anyone else living with epilepsy.
Epilepsy Blog Relay: Henry’s Fight with Dravet Syndrome
Henry at about 1 year old, started having seizures again but this time there was no fever. Our lives just changed forever.
Epilepsy Blog Relay: A way through a diagnosis of epilepsy
My first grand-mal seizure landed me in the hospital and really opened my eyes. When I received a diagnosis of epilepsy, I was just 23.
Epilepsy Blog Relay: Living With A Spouse Who Has Epilepsy
Mike admits, “when your spouse has epilepsy you will find it’s easy to help them. It may take a little extra work, but it’s worth it because you love them.”
Epilepsy Blog Relay: Jade’s keto journey
Jade shares how she took something that was crushing her spirit (epilepsy), and turned it into what drives her. She shares her own Keto Journey with us.
Epilepsy Blog Relay: Brain surgery reminds Teo of the importance of adaptability
Teo shares his story of brain surgery. He shares the importance of flexibility and the ability to adapt to every situation.
Epilepsy Blog Relay: Raising a child with multiple chronic conditions
Rachel’s son Andrew has multiple chronic conditions including Cerebral Palsy, Lennox Gastaut Syndrome and Cortical Visual Impairment. She shares a sneak peek into raising a child with special needs.
Epilepsy Blog Relay: Ways to help with medication costs
This post is part of the Epilepsy Blog Relay™ which will run from March 1 through March 31. Follow along! Alison’s Story Since my diagnosis with epilepsy in 2006, I feel like I’ve tried every medication possible to try and stop my seizures. My neurologist added Fycompa in 2016, I’m still not seizure free, but … Read More