A while back I started a new job as therapist. Having completed graduate school, I was so happy to be working in my field. Despite my excitement, my new job brought challenges. One of those challenges included management of my seizures. I developed new triggers and had to rework my daily routine … Read More
Sometimes, finding adventure means ignoring fears and jumping in with both feet. Going canyoning in Slovenia required just that!
People with epilepsy experience the impact of stigma everyday. In many cases this can lead to a sense of vulnerability and despair. Elaine shares how she deals with those feelings.
Stigma can make you feel ashamed, embarrassed and it can make you lose your confidence. Try to remember that you are not your condition.
Epilepsy is one of the most common conditions affecting the brain yet there is still a stigma associated with epilepsy. Could sharing personal stories create a tipping point to change the dynamic?
I’ve had epilepsy since I was 14 (now 31) and about 6 years ago I began to suffer from post-ictal psychosis.
I feel as though I am not alone anymore. What I struggle with is, in a way, normal. My brain doesn’t always function correctly and it causes seizures, but I am not alone, and I am not helpless.
Sometimes, in my fight to eliminate stigma and live a “normal” life, I create the perception that my life is easy and free from struggle. However, in my speech at the Epilepsy Foundation of Western/Central Pennsylvania’s (EFWCP) annual Mardi Gras Gala I showed what life with epilepsy is like–both the good and the bad parts.
