Epilepsy Blog Relay: Maureen vacations where epilepsy is considered a curse
People around the world believe that epilepsy is a curse. Maureen decided to spend her vacation getting to know a community that believes this about epilepsy.
Living Well With Epilepsy’s, Epilepsy Blog Relay™ is an epilepsy awareness movement to designed to maximize collaboration and eliminate stigma. Thanks as always to our generous sponsors and partners!
People around the world believe that epilepsy is a curse. Maureen decided to spend her vacation getting to know a community that believes this about epilepsy.
Fran Turauskis, founder and editor of Seize Your Adventure, has taken a moment out of her busy schedule to share her own epilepsy story.
If my child hadn’t been diagnosed with epilepsy, I’m not sure if I would know how to help during a seizure. Knowledge is power when it comes to first aid.
People with epilepsy experience the impact of stigma everyday. In many cases this can lead to a sense of vulnerability and despair. Elaine shares how she deals with those feelings.
Nancy Jane and her husband have shared the story of preparing for his brain surgery for epilepsy. They are ready for a better option.
Colleen and Paul, a teen newly diagnosed with epilepsy, are on a mission to make seizure safe schools a requirement nationwide.
Roman was diagnosed with epilepsy as a result of cortical dysplasia at the age of 3.5 months old. Learn more about cortical dysplasia here.
Meet Carolyn Parker Boyd: She’s an epileptic movie producer and she has a new project titled, “Where’s Gramps?”