but I do not think they would let him make us do it. Mr. Aldrin should know more about this than I do; he is a manager. So he must think Mr. Crenshaw can do it or will try to do it.
It is hard to go to sleep.
ON FRIDAY MORNING, CAMERON TELLS ME THAT MR. ALDRIN called him, too. He called everyone. Mr. Crenshaw has not said anything to any of us yet. I have that uncomfortable sick feeling in my stomach, like before a test that I do not expect to pass. It is a relief to get on the computer and go to work.
Nothing happens all day except that I finish the first half of the current project and the test runs all come out clean. After lunch, Cameron tells me that the local autism society has posted a meeting at the Center about the research paper. He is going. He thinks we should all go. I had not planned anything this Saturday other than cleaning my car, and I go to the Center almost every Saturday morning anyway.
On Saturday morning, I walk over to the Center. It is a long walk, but it is not hot this early in the morning and it makes my legs feel good. Besides, there is a brick sidewalk on the way, with two colors Page 30
of brick—tan and red—laid in interesting patterns. I like to see it.
At the Center, I see not only people from my work group but also those who are dispersed elsewhere in the city. Some, mostly the older ones, are in adult day care or sheltered workshops with a lot of supervision and live in group homes. Stefan is a professor at the smaller university here; he does research in some area of biology. Mai is a professor at the larger university; her field is in some overlap of mathematics and biophysics. Neither of them comes to meetings often. I have noticed that the people who are most impaired come most often; the young people who are like Joe Lee almost never show up.
I chat with some of the others I know andlike, some from work and some from elsewhere, like Murray, who works for a big accounting firm.Murray wants to hear about my fencing; he studies aikido and also hasn’t told his psychiatrist about it. I know thatMurray has heard about the new treatment, or for what reason would he be here today, but I think he does not want to talk about it. He doesn’t work with us; he may not know it is near human trials. Maybe he wants it and wishes it were. I do not want to ask him that, not today.
The Center isn’t just for autistic people; we see a lot of people with various other disabilities, too, especially on weekends. I do not know what all of the disabilities are. I do not want to think about all the things that can be wrong with someone.
Some are friendly and speak to us, and some do not. Emmy comes right up to me today. She is nearly always there. She is shorter than I am, with straight dark hair and thick glasses. I do not know why she has not had eye surgery. It is not polite to ask. Emmy always seems angry. Her eyebrows bunch together, and she has tight little wads of muscle at the corners of her mouth, and her mouth turns down.
“You have a girlfriend,” she says.
“No,” I say.
“Yes. Linda told me. She’s not one of us.”
“No,” I say again. Marjory isn’t my girlfriend—yet—and I do not want to talk about her to Emmy.
Linda should not have told Emmy anything, and certainly not that. I did not tell Linda Marjory was my girlfriend because she is not. It was not right.
“Where you go to play with swords,” Emmy says. “There’s a girl—”
“She is not a girl,” I say. “She is a woman, and she is not my girlfriend.” Yet, I think. I feel heat on my neck, thinking of Marjory and the look on her face last week.
“Linda says she is. She’s a spy, Lou.”
Emmy rarely uses people’s names; when she says my name it feels like a slap on the arm. “What do you mean, ‘spy’?”
“She works at the university. Where they do that project, you know.” She glares at me, as if I were doing the project. She means the research group on developmental disabilities.
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