I am creative, active and have usually been able to keep my Epilepsy from interfering with me living my life. There have been chunks of time where I have failed in this endeavor. The treatment and understanding of E has evolved since I was younger and I am discovering a new understanding of my 'issues'. There are so many times in my life where the medical community has completely failed to provide any information or even belief of my 'symptoms'. I am amazed, yet so sad. How different could things have been?