This post is part of the Epilepsy Blog Relay™ which will run from March 1 through March 31. Follow along! Beth’s Story Beth tries to post regularly about a number of issues, ranging from her interests in business anthropology, talent management, career advice and her own journey with epilepsy. What is true, regardless of her … Read More
Most people are not aware of an illness until it touches them personally. So, Shonet started thinking about creative ways to raise epilepsy awareness.
I hadn’t had a seizure in months so I should’ve been happy. But, I was miserable. I didn’t realize my depression was a side-effect of my medication.
Shonet shares examples of epilepsy and fatigue in her own life and a few tips to actively avoid getting to the point of total exhaustion.
After the loss: Tonya always thought, because she was older and had more seizures, SUDEP would steal her away first. Instead, the family lost Jesy to SUDEP in 2012.
My epilepsy may not consume my life, yet it keeps my adventurous and daring soul from running free.
After years of mental and physical trauma from seizures, Michael discovered what he wanted to acomplish as a person, and as someone diagnosed with epilepsy.
Nancy remembers how her temporal lobe epilepsy (TLE) seizures always began with a feeling of deja vu and a sensation of falling.