My now 3.5 year old son was diagnosed a year ago with Doose syndrome via mutation of the SLC6A1 gene, he had started having seizures at 5-7 months of age and I had attempted to address this with our pediatrician and the referring neurologist for a year before his actual diagnosis but it took his seizures changing presentation to drop seizures in the bath tub before they sounded the alarm of possible seizures and scheduled our first EEG. He is currently taking 5ml of Keppra twice a day and Levetiracetam 8ml twice a day and an accompanying 50mg of vit B once a day. We haven't had any break through seizures in a few months that I or his dad, or school teachers have noticed (although I am not completely confident his school environment is as attentive as I would hope). Does anyone here have any experience with these two diagnosis that they could provide stories and opinions on? We haven'y had many interactions with his specialists since not having breakthrough seizures and I want to be relieved but also don't want to be missing anything. His Speech development is delayed enough that we qualify for early preschool intervention and I am seeing some improvement but maybe not enough?