serenity wrote:
No, I don't have a dx, so it was validating, but it was also a little embarrassing, too. I can't help but wonder if all my sons' teachers, and paras chat about the possibility of me having AS during their lunch after an IEP meeting. Do you think that you'll ever go get an official dx, ChatBrat? I think I may someday when I can scrape up enough money.
I'm afraid to. I've had to fight tooth and nail to get dr's take me seriously as it is with my physical problems. I'm so afraid that they'll think I'm
looking for something to be wrong with me. Dr's and counselors hate it when you try to
suggest what the problem could be. They think it's only
their job and you're not supposed to read about anything medical in books or the internet. If you haven't slaved in college/university reading hundreds of books and heard an ungodly amount of lectures for many years, you're supposed to sit there and keep your mouth shut.
I think what I'll do someday is, instead of going through my HMO, I'll save up and pay for a private session with someone known to work with and diagnose AS people (I might have to go to a big city for that.) If I get diagnosed with it, I can eventually let my PCP know. If I don't get diagnosed with it, I won't let my PCP know that I sought help and he'll never be the wiser.