Epilepsy Blog Relay: Kat’s take on medical marijuana and epilepsy
Kathryn shares personal anecdotes about her seizures and memory loss. It includes a candid discussion about medical marijuana as a treatment for epilepsy. … Read More
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.… Read More
Epilepsy Blog Relay: Alison on building your family when you have epilepsy
Blogger, Alison Zetterquist, hid her epilepsy for almost 35 years because of her own embarrassment. Now she shares tips on building a family of supporters.… Read More
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. … Read More
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.… Read More
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. … Read More
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.… Read More
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