Epilepsy Blog Relay: Suicide and the stigma of epilepsy
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.
Leila’s Ideas: Starting a New Job
Earlier this year, I started a new job as therapist. Having completed graduate school in 2015, I was so happy to be working in a field … Read More
Traveling with Epilepsy: Finding Adventure in Slovenia
Sometimes, finding adventure means ignoring fears and jumping in with both feet. Going canyoning in Slovenia required just that!
Epilepsy Blog Relay™: Do you KNOW Epilepsy? Say NO to stigma
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 Blog Relay™: Eradicating the Stigma Surrounding Epilepsy
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?
Jenny’s Story: I’m not afraid anymore
I’ve had epilepsy since I was 14 (now 31) and about 6 years ago I began to suffer from post-ictal psychosis.
Rachel’s Story: I am not alone anymore
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.
Leila’s Ideas: Speaking about stigma at the Mardi Gras Gala
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.