Educated Guesses
October 23, 2008 by Kristina Chew, PhD
Filed under Health

After being so very tired on Tuesday, Charlie got himself out of bed on Wednesday morning, got dressed and zoomed out the door sans sweatshirt and bookbag before either Jim or I could shove on our shoes. After a tough couple of days at school, Wednesday was very good.
Jim had suggested that keeping Charlie in motion (especially out of doors) might help. Last year Charlie had Adapted Physical Education at 11am, just around the time he was getting sluggish and his energy was ebbing. This year, he has gym at 8.37, right after he gets to school. That means he’s active first thing in the morning, perhaps gets a bit tired from the workout, and then has a long day of working at his desk, learning pre-vocational and life skills (his class has the use of a home-ec room’s kitchen and also a washer and dryer).
Charlie’s teacher and the consultant followed up on Jim’s suggestion and had Charlie go out for walks periodically on Wednesday and this helped a lot. I can sit for hours in a chair and work and read. Charlie (like Jim) needs to get up at regular intervals—half hour, twenty minutes. I’m sure the crisp cool air also helped to wake him up; no doubt the heater has been turned on for his school. Charlie’s classroom has windows that open onto a hallway, but no source of direct fresh air. As I know from watching my students as I taught them the third declension of Latin nouns yesterday, cold day, warm classroom, something difficult to attend to—-these can all be the ingredients for dozing off.
Charlie’s alertness and his spontaneous language continued for the rest of the day. He got off the bus and, after running a card through the Language Master, told me “I had a great day.” He told me “carrots” and then “I need help, bag” and I got out a plastic Ziploc and handed it to him; Charlie packed it full of baby carrots. He said “grapes, please” and asked for “help” and I got him another Ziploc and he packed that one really full with purple grapes, carefully pulling many off the stems. There was a final request for help to seal the bags and he put them his lunchbox, zipped it shut, and placed it on the top shelf of the refrigerator.
Then he asked to play cello. As I brought the cello into his room, he asked for the bow.
We usually go bowling with some other families with autistic kids his age on Wednesday. Charlie said no to this and requested a walk which, under a brilliant blue autumn sky and with loads of leaves to crunch in, made for a very nice time together. Then we made our way through Jersey commute traffic to pick up Jim at the train.
I know I don’t, can’t, know what’s really going on in Charlie’s mind. The words Charlie says (so far) don’t readily explain how he might be feeling. Over the years, in unspoken recognition that language is not the easiest mode of communication for Charlie, I’ve become a serious student of the educated guess. I still write every night about Charlie’s day in a journal as I’ve done since he was a baby and this exercise has been a way to note patterns of occurrences. I try to write down, as much as I can, only what Charlie did, what we did; what I saw.
Jim, further, has a good instinctual sense for what Charlie might be feeling, whether nighttime hyper bouts or anxiety so intense that it makes you freeze up. So we continually guestimate what might be the reason for an afternoon of intermittent shrieks, for a sudden need to run run run run run.
Those things happened on Tuesday afternoon; I suspected unusual stomach trouble, and this proved to be the case. I’ve heard it said more than a few times that, isn’t it something awful that a child can’t explain in words that he or she has terrible pains in their stomach or head. Charlie can’t tell us those things in words, yet, but that’s meant it completely behooves us to understand him on his terms. Sometimes we’re so wrong you’d wonder why we bother; other times, we kind of figure it out.
Yesterday after getting home, Jim proposed a father-and-son dinner. I handed Charlie a new dark blue hooded sweatshirt, as the one he’s worn for the past year needed a good washing. He’d said an adamant “no” to the new sweatshirt when I first showed it to him. Yesterday night, after I had explained that we had to wash the other sweatshirt, Charlie pulled on the new one. He adjusted the hood—far bigger, and lined in soft, new fleece—on his head and shoved one hand at a time in the big front pocket. It’s an adult size small so he has some room to grow into it and the hood didn’t hide so much of Charlie’s face that I couldn’t see him smile happily.
After he and Jim went out and came back and Charlie was asleep, I took out some of the carrots and grapes from the bags Charlie had packed. Even a boy growing and growing up pretty fast can only eat so many carrots.















I love to hear about your experiences as a parent. And even though my guys are much more verbal, I still find myself guestimating what they are feeling at times. It appears to me that having more words does not equate to the ability to express one self’s thoughts or feelings in any level of the spectrum.
Isn’t it funny (and not funny ha ha) how parenting a special needs child is like a great mystery and us parents are the detectives. We are always analyzing things to figure out how it all fits together and solve the issue.