Epilepsy Blog Relay™: 7 Things I Wish I Had Known About LGS
Kelly’s Story: The seven things I wish I had known before my daughter was diagnosed with Lennox-Gastaut syndrome (LGS).
Kelly’s Story: The seven things I wish I had known before my daughter was diagnosed with Lennox-Gastaut syndrome (LGS).
Kat’s Story: I am an artist, an author, a jeweler, a mother, a wife, and a writer. Epilepsy is simply a part of my life, as much as every other thing.
Heidi’s Story: I realize that more people need information about Epilepsy that is why I started the page Epilepsy Education and Support.
From Soo: Caregivers are the unsung heroes in the fight to gain seizure freedom and help us living with epilepsy achieve a fulfilling life.
On day 5 of the Epilepsy Blog Relay™, Carys reminds us “We can battle this together and educate society!”
As part of the Epilepsy Blog Relay™, I share why I am thankful to be living with Epilepsy.
Day 2 of the Epilepsy Blog Relay™ Don’t miss Beth Schill’s post on http://anthrosuit.blogspot.com/. Beth’s site, [Per]Suit of Anthropology, is a blog dedicated to the exploration of modern business trends and perspectives from the view of anthropologist, with a special emphasis on cultural understandings of work-life balance and disability rights in the workplace. … Read More
Thank you for reading my March 2017 Epilepsy Blog Relay blog post. I’d like to talk a little bit about Epilepsy in everyday life, including why I am working to share my own story.