I am new to this seizure thing, and still learning what is causing mine. I have been trying to learn as much about things as possible. My mom is big into the Gluten stuff, having our whole family tested for sensitivities to gluten. I am staying off it for the most part, but haven't really noticed much of a difference. I have a question regarding how the neurologists take this.. Mine doesn't seem concerned with gluten playing a part in seizures at all. Have you ran this by your regular team of Dr's, and if so, what do they say? I am noticing that most of the neurologists just want to shove pills down us and not explore what the CAUSE of the seizures are. Anyone else experiencing that when discussing the gluten issue?