Finding real support in the online epilepsy community
Hayley has shared her experience with online epilepsy support communities to help those who are newly diagnosed with epilepsy.
Hayley has shared her experience with online epilepsy support communities to help those who are newly diagnosed with epilepsy.
Regardless of who you’re working with to manage your epilepsy, open and honest communication with your healthcare team is a priority.
Lisa’s Story It was December 2007 and I had been suffering with awful, constant headaches for the past 2 years and had been going back and … Read More
Emily shares some insight to living with Epilepsy as an adult including how to handle work, transportation, stigma and anxiety.
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.
Like many people diagnosed later in life, Jewel had little knowledge of what Epilepsy was, and what life would be like living with it.
On 6/30 at 7pm ET, we will host our next #LIVINGWELLCHAT. We will hear from the community on what the new marijuana-based epilepsy drug could mean for families affected by LGS and Dravet Syndrome.
Many people have asked me what my seizure triggers are. So, I thought I would tell you both my triggers and what tools I use to combat them.