Daniel Willingham is a professor of psychology at the University of Virginia, where he has taught since 1992. His research once centered on the brain basis of learning and memory, but for more than 15 years, he has focused on the application of cognitive psychology to K-16 education. He was appointed early this year by President Obama to be a member of the National Board for Education Sciences, the independent and nonpartisan arm of the U.S. Education Department, which provides statistics, research and evaluation on education topics.
In this post, Willingham writes about something different — his family — and he offers an unusual lesson for everybody. He can be reached at firstname.lastname@example.org and you can follow him on Twitter @DTWillingham.
By Daniel Willingham
March 18 was National Trisomy-18 Awareness Day. It’s important to me because one of my daughters, Esprit, has Trisomy-18. In the spirit of the day I’m going to offer just a little background for those who are unfamiliar with it, but focus mostly on one interaction small children typically have with Esprit — staring at her.
By way of background, Trisomy-18 is a chromosome disorder. Each cell in the human body has 23 pairs of chromosomes, strands of DNA. Trisomy means that there are three copies, not two, of one of the pairs. Three copies of the 21st chromosome is Trisomy-21, also called Down syndrome. Three copies of the 18th chromosome give you Trisomy-18, also called Edwards Syndrome. (So now you know why they picked March 18 — 3/18 — as Trisomy-18 Awareness Day. )
There’s no particular cause for the disorder; it’s a fluke. There’s also no cure, and more than 90 percent of children born with Trisomy-18 die before they turn 1.
Esprit is unusual for still being here at age 13, but her profile is typical of Trisomy-18 in other ways. She cannot walk or speak, and she learned to sit upright about a year ago. Cognitively, she’s like a 1-year-old on many dimensions.
My goal here is not to raise awareness about the medical side of Trisomy-18 — if you’ve read to this point, you’ve come close to the end of my knowledge — but rather to consider the manner in which you are most likely to encounter a child with Trisomy-18 when you are out and about with your own child.
Older kids (and their parents) will sneak a surreptitious glance at Esprit. Many adults will smile and some will approach her, always with warmth. But kids ages 2 to 6 are generally flummoxed when they see her — and show it. Parents are usually not prepared to respond to their child’s curiosity and bafflement.
Your 5-year-old will notice that Esprit doesn’t look like other children. She has facial features typical of Trisomy-18 kids. Her head is small, her ears low-set, her chin recedes and her eyelids droop, so she usually looks sleepy.
But your child wouldn’t be paying attention to these facial features because others are much more noticeable. Esprit is tiny for her age, weighing just 50 pounds, and she’s usually in a large wheelchair that provides support for her back. She also wears a TLSO (a brace) around her midsection, and orthotics on her feet.
To a 5-year old, this is a sight.
So usually he stares. (I’ll call the child “he” to keep pronouns unambiguous, with “she” meaning Esprit.) That makes the parent uncomfortable, and they try to call the child away, distract him, so he’ll unlock his gaze. The parent doesn’t say “don’t stare”; doing so would acknowledge that he’s staring and that there’s something to stare at. Eventually, the parent might drag or chivy the child away, with the child looking back the whole time, staring.
I appreciate that you don’t want your child to stare, but ignoring his interest or trying to rush away doesn’t work well and sends your child the message that there’s something wrong here. Admonishing the child once out of earshot by saying “it’s not nice to stare” will not make him accept a disabled kid as part of the shopping mall crowd next time he sees one. Kids this age are too young for that. (If there’s any effect, it will be to make him a sneakier starer.)
Here’s an alternative. Encourage your child to add a social element to the staring. It’s natural and unobjectionable that he’s curious about a child who looks different. Staring feels wrong because interaction with another person demands some outward acknowledgment that there is a fellow human in front of you. You can gape at a skyscraper or a sunset, but no matter how interesting another person is to behold and for whatever reason, you must give social signals that you recognize that they are not an object.
Once you add social signals, staring doesn’t feel like staring. Staring while smiling, for example, seems perfectly appropriate. Sure, a 5-year-old’s voluntary smile is comically phony, but who cares? It’s the thought that counts. Or encourage your child to say “hi” or to wave. Any of these changes the dynamic from “observation of a spectacle” to a bid for social interaction. (It will also thrill Esprit.)
More outgoing kids will ask questions, usually of my wife or me rather than Esprit. Please don’t shush them, and please don’t worry about what they will ask. Parents (and strangers) don’t expect social graces at this age, so we know we’ll hear, “What’s wrong with her?” or “What’s that?” (pointing to her orthotic). We’re very used to talking with children about Esprit’s disability. Questions are a way of initiating social interaction. They’re great.
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Each family’s experience is different, of course, and I’d never claim to speak for all parents of disabled children. But the next time your little one stares at someone different, give the social signal strategy a try. Let me know how it goes.
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