Hi everybody, thanks for all of your help.

I had my last straw with this neuro. See, we see the neurologists at Barrow Neurological Institute in Phoenix and I have faith in their reputation but some are a little too, well, shall I say confident. I fired him and moved over to another neurologist and she was absolutely wonderful. She decided not to order another EEG. Won't help. We are already know she has tons of seizure activity. She ordered levels to be drawn and her tegretol was low, once again. We upped her dose another 5 ml. Gave me some Klonipin wafers and we are good to go. She was an absolutely amazing doctor. She stated that if Emma has another seizure, she is changing meds.

Also, get this, she actually spent 45 minutes sitting with me and reviewing my daughter's MRI imaging WITH me.

I know somebody asked in the other forum (this was originally under the TBI thread but a mod moved it) when she gets them. She has only had these early in the morning. Sigh. My poor baby.