Making adjustments and finding gratitude Living well with epilepsy to me isn’t about being seizure free. It isn’t about wishing I could drive. It isn’t about wishing I didn’t have to take pills every day, and it isn’t about wishing I could be in a different job. Living well with epilepsy to … Read More
Are you new to Epilepsy? Have you had a recent diagnosis of epileptic seizures in your family? Maybe I can help ease the anxiety with this column.
Dear Mum, You were there to hold my hand on my way to the first of many tests for Epilepsy diagnosis. The one who smiled at me with so much love to ease my fears through the old door window as I lay there all wired up to the EEG. You laughed … 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.
Purple Day 2017 is quickly approaching! Join Emily and get and share ideas to celebrate and support one another on March 26, 2017!
Looking back on 2016, I realise it may have been the most exciting year ever, including a Champion Award and a Wing Walk among other amazing adventures.
This post is part of the Epilepsy Blog Relay™ which will run from November 1 through November 30, 2016. Follow along! Emily’s Perspective It’s the most wonderful time of the year!!! Christmas and wintertime are my favourite time of year, and for so many others too, but this festive season can be … Read More
In 2006 I was diagnosed with Epilepsy. At the time I was confused; we all were. I have written quite a bit about my general experience but basically, I grew to adapt to my seizures and new lifestyle and I just got on with my life. I was nearly 11 and I … Read More