When my son was very young, we discovered he had epilepsy. He was only six weeks old and we were at his baby shower. Our typical life ended and we were thrown into the world of special needs. For the first year we focused on keeping him alive. For the second year we searched for as much normalcy as we could find. We were very lucky and got (knock wood) control of his seizures last year with the help of the Ketogenic diet and a couple seizure meds. I can breathe a little easier now. I can think a little clearer now. I want to make sense of all we have been though, will go through. I want to help others going through this insanity if I can. This is why I have decided to blog. I know it will help me, and I hope it will help you.