This post is part of the Epilepsy Blog Relay™ which will run from March 1 to March 31, 2018. Follow along! Emma’s Story Emma’s blog, Little Mama Murphy, shares stories from a family living with the ‘medical mystery’, of an undiagnosed child. Stories include stressing about coming to terms with the lack … Read More
Day 7 of the Epilepsy Blog Relay™ Epilepsy Education and Support was created to provide information and support for people with Epilepsy, caregivers and those who are interested in Epilepsy all over the world. Heidi’s Story I realize that more people need information about Epilepsy that is why I started the page … Read More
This post is part of the Epilepsy Blog Relay™ which will run from March 1 to March 31, 2018. Follow along! Living Out Loud In 2008, Jewell’s life drastically changed. She was diagnosed with a seizure disorder and since then, she has endured many EEG’s, EKG’s and MRI’s in an attempt to … Read More
This post is part of the Epilepsy Blog Relay™ which will run from March 1 to March 31, 2018. Follow along! Day 4 of the Epilepsy Blog Relay™ Sarah Louise joins the Epilepsy Blog Relay with an update from her site, Miss Sarah Louise’s Masterpieces and Munchies. She shares her experiences with … Read More
Jes Armstrong is back again to share an update from her blog Wishes for Mercy, a blog about her experiences as mother to a special needs child who looks normal at first glance. … Read More
As 2017 comes to a close, I thought I might take a minute to share Living Well With Epilepsy’s top 10 epilepsy stories this year. … Read More
We are coming to the end of our November Epilepsy Blog Relay™. As always, we will close with a live #LivingWellChat on Nov 30, at 7pm ET.… Read More
From Randi: I’m looking forward to everything that comes with having a newborn baby, but there is a cloud of guilt and sadness hanging over me.… Read More