Hi hed,
I'm glad you have a different neuro. Some of them are very arrogant. They let all their education go to their heads. My first neuro/psych was great. He wanted me to be fully involved in my treatment. I really missed him when he went to practice at a psych hospital. The only problem with him was he told me I had a seizure disorder, but never explained it, he focused on the depression (bipolar actually). He treated me with meds that treat both disorders. Anyway, I wasn't as computer literate as I am now & didn't look into seizure disorders. Oh, please keep in mind that some meds do treat depression & epilepsy. On the other hand some AED's do cause depression.
After he stopped treating me, I saw a regular psych who didn't know about my epilepsy. I only saw him for about a year. I was still on Trileptal prescribed by a different neuro. Then I lost my insurance & quit the psych (actually he quit me, saying he couldn't hel me any more for the bipolar) & weaned of trileptal. Within a year I was having lots of seizures. I went another 1 1/2 years before my family doctor suspected seizures & sent me to my current neuro. (I didn't suspect seizures since my 1st neuro never talked about them.)
The first time I saw my current neuro/psych, he was totally arrogant, said if I wasn't losing consiousness that I wasn't having seizures - which as we all know is nonsense. When he ran the EEG & confirmed "very active seizure activity", he started med for the seizures, but since I'd already been on all depression meds except MAOI's, he didn't focus on the bipolar. Anyway, as I was saying, he was still very arrogant. So after that visit, I did a ton of research. I went back and was able to describe & name every type of seizure I have, and even say why doctors say "seizure disorder" instead of epilepsy. He was amazed at my new knowledge & it reflected in his attitude & treatment toward me.
Then I learned about keeping an ep diary. When I took it on my visit in November, he said it was great. He sat there & read over it, counting the number of each type of seizure, everything. He was glad to have it.
Have you found a good ep diary yet? Are you going to just write one out or are you going to do one on a web site? I use one from a web site. There aren't very many diary web sites, but I think they are better than one you write out by hand. They are more uniform & easier for a doctor to read over quickly, which as we all know, is very important since we have little time with our doctors. I'll give you the site if you are interested.
Have you been able to determine yet whether your depression started before or after your onset of epilepsy? I know that can be difficult to determine. Seizures can definately mess up our memories. Maybe family or friends can help you determine when your depression started.
You mentioned a dream. Is it the same dream all the time? I have the same recurring dream - standing in the hallway of my old school, not knowing where to go, feeling lost. I thought it might be seizure related because it is similar to one type of seizure I have. But I was assured that it wasn't a seizure. But it was also suggested to me that I talk to my psychologist about it. I haven't gotten around to it yet as we seem to have so many other things to deal with. Bipolar w/o any meds to treat it is vey difficult to say the least. Then add PTSD & anxiety disorders. I keep him busy.
Well, sorry to ramble on like this. I totally understand your depression & your frustrations with arrogant neuro's. Let me know if you want the web site for the ep diary & if you want to use it, I will tell you how to copy & format it in a way that will make a doctor more willing to read it. You can send me a private message if you want. Take care
Shelia