Funny how it feels like i'm waiting for something horrible to happen everytime we start a new drug. I wake up in the morning and wait until Carrie comes into my room. I'm listening for the seizures that only happen in the morning. She lays in my bed and listens for Darren's seizure while i go have a bath. I should probably just wake him up but it took him forever to fall asleep last night. I thought all these aed's made a person tired. It sure hasn't gone that way for Darren. He started at 250 mg of Keppra last night on top of the 25 mg clobazam/day that he is already on. I've having to put it in his mouth myself as i've found his meds untouched at the breakfast table once or twice and that is too many with 5 little children in the house!! He is not pleased with this treatment but there is nothing else to do.