Emily’s Perspective: My Family’s Epilepsy Experience
Epilepsy doesn’t just impact the person diagnosed, it also effects the entire family. Emily shares her family’s experience and offers advice to others.… Read More
Epilepsy Blog Relay: Emily’s perspective on the SmartWatch
The SmartWatch is a new device that will monitor movement and detect any abnormal patterns in motions such as any experienced in an epileptic seizure.… Read More
Emily’s Perspective: Young Epilepsy Champions 2016
Young Epilepsy Champions Awards will celebrate the achievements of children and young people with epilepsy.… Read More
Emily’s Perspective: Remembering my first seizure
I often talk about today, and what has been going on in my life. This month I’d like to do a bit of a ‘throwback’ and remember my first seizure.… Read More
Emily’s Perspective: Home Treatment
This month I am going to be focusing on home treatment for Epilepsy. There are a few things you can do to make things a little less stressful or tiring.… Read More
Emily’s Perspective: Facts and Myths about Epilepsy
Do you know the differences between facts and myths surrounding Epilepsy?… Read More
Emily’s Perspective: What one word describes how you feel about epilepsy?
This post is part of the Epilepsy Stigma Blog Relay which will run from June 1 through June 30. Follow along and add comments to posts that inspire you! I have always worried about work. Do you need to take time off after a seizure? How long should you take to recover? … Read More
Emily’s Perspective: Back to the working world
I’m going to be 21 in a few months and generally, Epilepsy aside, I am in a pretty healthy condition. Just recently I was given the all clear for working with Epilepsy. That means I am fit to work even though I still having a seizure every now and then. But that’s … Read More