Has anybody been to OHSU for treatment? I have read they have a good program. My neurologist seems good, and I like him, however, I am not yet stable on my medications, and it is nearly impossible to get through his nurse. I am on my 6th medication since October, because of hives, allergies, or I:? cannot tolerate the side effects. I had such a bad time with the Keppra-I tried to call, my husband called, and was told to call my Primary care doctor. My primary care doctor called him as she does not feel qualified to change these medications, and was told I would get a call back. After 2 days, I called her back, as I had not gotten a call back. She called again. She checked back a few hours later, to see if they had called-when I told her no, she called them again, and ripped into them. I finally got a call back from a nurse changing my meds. All of this took 2 horrible weeks. I am having several seizures a day again, and a nurse called today to tell me to double my meds, but I would like to go in to see my doctor to see about my sleeping issue as I have not seen him in 3 months. I cannot get an appointment until August 22nd. Does this seem right for a person that has only been diagnosed since last October, and has not found the right medication, or combination of medication to get myself stable, or at least in a state that I feel like I can function as normal as possible. I am new enough at this that I do not know if it is normal that I should have to wait so long to get in, or wait that long to at least get a call back.