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Monday was the day of G’s full evaluation, the one we’ve waited for over a year to receive. We spent the day answering questions, listening to G answer questions, watching G be examined physically, watching as G played and interacted with the doctors. I went through it all, my stomach in knot, wondering what each doctor was writing down, if G was doing things “right”.
At the end of the day, we spoke with the doctor while G played computer games in the next room. The first thing that she told us, was that G was astoundingly smart. In fact, he has and IQ of 122 (confirming once and for all that my children are indeed smarter than me). With that said, she went on to explain that G did in fact have a mild case of Aspergers.
Even though we have known that for so long, finally hearing it out loud still hit me, making my brain freeze and stealing the air from my chest for a brief moment.
We were told to start G on Melatonin for his sleep problems, and to look into getting him OT through school, and exploring socialization groups. She advised us to stay calm in the midst of his fits, to help him with joint compressions, and to stop struggling so much over food. She told us to look into the Maine Autism Network, and wished us luck, assuring us that G was a wonderful and extremely bright boy.
And G is still G no matter what. His amazing teacher called me yesterday to let me know she was having G join a new math club at school, and he continued to be a “dear” in his classroom. Last night we struggled through yet another meltdown. Tonight, we will begin the Melatonin. Now that we k now for sure what’s going on, we can work to help G the best we can. And maybe find a little help for ourselves along the way.