Morgan’s Epilepsy Story Morgan shares her epilepsy story about living with Temporal lobe epilepsy. Morgan’s epilepsy story was first published on the site in 2012 When I was 15 months old, I had my first seizure. I had been sick and running a very high fever. According to my mom and my … Read More
Steve Wynn In March of 2010, Michael Gomoll lost his son suddenly to Dravet’s Syndrome, a rare form of epilepsy. Gomoll then established The Joseph Gomoll Foundation to honor his son, and began preparing for the release of the Joey’s Song project. One of the leading supporters in the Joey’s Song … Read More
Our last post provided you with information on a project called Joey’s Song. The project was created after Joey Gomoll succumbed to Dravet (pronounced Dra-vay) syndrome. This rare form of epilepsy robbed Joey of most of the ability to speak, but it didn’t stop him from communicating with everyone he met … Read More
When Michael Gomoll lost his son Joseph Martin Gomoll suddenly in March of 2010 to Dravet’s Syndrome, a rare form of epilepsy, he decided to take action. Gomoll turned his pain into an opportunity for those living with epilepsy. He established The Joseph Gomoll Foundation to honor his son and since it’s inception, the … Read More