Living up to Expectations
Well, we spent our two hours with the psychiatrist yesterday. And I got good news, more good news, and bad news.
The boys liked him, he was pleasant, easy to talk with, good and handling me ... so what's not to like? They relaxed and showed him their true selves. They were polite with thank you, please, no thank you and you're welcome. Oh and "may I please ..." a couple of times. But they were all over the place. Tucker ran laps around the table while he was answering questions. Michael answered the questions that he heard rather than what was really being asked.
I expressed my concern for Tucker's self-esteem. I mean right now anyway, he seems not to have any serious esteem issues. But what must it be like for him to live in a world where he's redirected, told to sit down, told to pay attention, told to finish his work, singled out a hundred times for every one time that the kid next to him is given the same feedback. How many days can that go on before he starts to wonder what's wrong with him? And the doctor uncovered a little of that already happening when he interviewed Tucker.
At the end of the session we left with a prescription for both of them to address ADHD and the recommendation that they both be signed up with a psychologist for group therapy to address specific behavioral and social issues.
The doctor did not give us the diagnosis I was expecting for Michael. He looked at all the different aspects of autism and said what I've heard before. He doesn't fit neatly into "Autism" because he's too high functioning, but he doesn't fit into "Asperger's" because he has language disturbance. SO the diagnosis remains "Pervasive Developmental Disorder, Not Otherwise Specified." That makes it harder to deal with the school because they really need that word "Autism" on a piece of paper before specific services are authorized to help him. ~sigh~
The doctor talked with me for a long time. Asked a lot of questions about the past year, what had happened with the divorce, and how the kids were doing now. I don't think you have to be a mind reader to know that I've worried a lot about this. I've felt guilty that doing the right thing for me was exactly the wrong thing for my kids. And I've thought that was a mistake. They are kids. They need to be put first. What does it mean for them long term that they have had to make the adjustments they've made? What does it mean for us as a family that we haven't been able to give them 100% of the support they have to have to make it? I mean, it's hard enough for "normal" kids when things happen. But when you have kids who have ... problems like my kids have, it seems to me that it's exponentially worse.
So I was expecting that he would talk to me about the damage and tell me things about how to undue it, or work to restore ... but he didn't. He looked at the kids, watched the way they interacted with me and with each other. And then he said the words that finally broke me down and had me bawling. "You are a good parent."
After that appointment I was so emotionally drained that I just came home. It was a lovely day. The kids played outside for a little while. And I just vegged out. I needed to do that. I talked to a couple of friends. Drank a diet coke ...
Then we swung by the library and picked up a few books. Went to the pharmacy and filled their prescription. Happily, it's the kind of med that should tell us within a few short days whether they are being helped. So we start that this morning. Wish us luck.
I haven't been keeping up with your sites this week. And I'm sorry for that. It seems that when I get emotional, I just can't sit still in my chair long enough to read.
Please don't give up on me. I'll be back around.
Terri
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