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.… Read More

Epilepsy Blog Relay™: How a diagnosis of LGS connected one family to an entire community

This post was written by Elizabeth Terry, a historian and author in St. Louis, and mom to Spencer who has Lennox-Gastaut Syndrome (LGS). Living Well With Epilepsy is grateful to Lundbeck, a Sponsor of the November 2015 Epilepsy Blog Relay™. I remember my husband and I whispering to each other, “Is this … Read More

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