If I were you I would definitely ask my psychologist for a copy of anything she sent to social security - if she is willing to release it to you. It is very hard to tell what is going on in your case until you read your records.
I second this but suggest not to just ask her but also get copies of what the social security itself has received (this can also be done throu legal means). I actually had two male workers in the social security office sabortage my case so I believe i was knocked back twice due to them.
These two had previously told me they didnt believe in ME/cfs and actually said they would make sure I didnt get benefits. Fortunately on remembering these comments after the 2 time I appealed was rejected and I couldnt figure out why as I had great backing info to my case and I was so sick that I couldnt even stay seated and had to lay for appointments
so on my third and final appeal just before it was just for assessment, I then wrote for a copy of everything in my files backing my case only to find that my supportive info wasnt in fact there and had been removed and vanished so had been missing from the assessments. (some of that had been previously posted in and other of it had been directly handed to them over the desk unfortunately going throu the two guys who didnt believe in ME/CFS).
i can only wonder just how many people with ME these two stopped from getting benefits.
So I highly advise everyone to check that the place where your assessment is being done has ALL your info. Dont only trust they have it.
The assessor (my case ended have having to be assessed in another state) told me had that info been there, I would been granted the first time and wouldnt had to go throu 3 appeals.