Is autism really a “problem?”
Filed Under (Acceptance, Adam, Autism and Intelligence, Autism and Learning, Communication, autism) by Estee on 20-02-2010
We’ve had some encouraging messages lately, haven’t we? The HBO production of Temple Grandin played by Claire Danes shows that while (and many of us have read Temple’s books already) the world caused her anxiety, she could “see details other people are blind to,” she says. “I have a gift.”
Certainly the idea of giftedness, which happens in non autistic and autistic persons, can be yet another stereotype in assessing autistic people. Perception, on the other hand, is something to think about deeply.
When Adam was very young, we had these water blocks that were dyed different colours. Adam was mesmerized by these blocks watching the water swish and swoosh. Then all of a sudden, my wobbly toddler took them up to the window and peered through them. Ah, I thought. If only we could all stare at the world through coloured water blocks. How beautiful it would be. I know was also in part a cooing mother of a young autistic boy, so anything he did like this made me hyper-aware. But still.
When he got his “legs” and we began walking around the neighbourhood, Adam memorized his routes. To this day, if we take him to his old house and walk from there or the park nearby, he will remember how to get to that park or get back through the old “secret pathway” to the old house — which has even since been torn down and rebuilt! Remember, that was his two-three year old brain. In April, he will be eight-years-old.
Coming out soon will be a new version of Lewis Carroll’s Alice in Wonderland, directed by Tim Burton. Many people suspect that Carrol was himself autistic with his different perceptual abilities. He is often cited as a person who “suffered” from micropsia and macropsia, which is a neurological condition that changes the way the brain perceives the size of objects. When Alice falls down that rabbit hole, we get a look into Carroll’s mind.
Scientific American Mind published Extraordinary Perception by Wray Herbert this month. It discusses how psychologists at University College London “think that it might be a mistake to consider [autistic] distractability as simply a deficit. To the contrary, Anna Remington and John Swettenham and their colleagues speculate that people with ASD might have greater than normal capacity for perception, so that what appears as irrelevant distraction is really a cognitive bonus.” I added autistic to distractability as many therapies for autism as well as medications are geared at lessening it.
The test, the article shows, was for subjects to “rapidly determine if the letters N or X were present in the ring” on a computer screen. Participants had to then “hit the corresponding key on the keyboard. Some of the circles — those with more letters — were more difficult to process than others. There were also other letters floating outside the circle, but the subjects were specifically instructed to ignore those letters. Those floating letters were the laboratory equivalent of an irrelevant distraction in the real world.” In measuring perceptual capacity, researchers saw that “everyone was slower at the task when the ring contained more letters. The researchers were also measuring distractibility. When a letter outside the ring was one of the target letters (N or X), the subjects often took a longer time finding the N or X in the ring — indicating they were distracted by the presence of a target letter in the location that they were supposed to ignore.”
The researchers reasoned “that as long as the subjects’ total perceptual capacity was not exhausted, they would also process the irrelevant, distracting letters within their visual field. Once they had surpassed their perceptual capacity — once the ring of letters was sufficiently complex — irrelevant processing would stop [bold mine]. So if ASD subjects in fact have greater processing capacity, then they should process more distracting information even as the main task becomes increasingly complex.”
In conclusion, “although there was no difference among subjects in either reaction time or accuracy on the main task, those with ASD processed the irrelevant letters while solving much more complex problems...Put another way, they weren’t ignoring the main task, nor were they distracted away from it. Instead they were completing their work and moving on, using their untapped capacity” [bold mine].
This article also concludes that while this is a benefit, it also does have “real-life consequences.” They begin and end the article citing Tim Page, an author with Aspergers from his book, Parallel Play: Growing Up With Undiagnosed Asperger’s. Page recounts his time in school who failed an essay about his field trip which was quite detailed in terms of his way of perceiving it, and how he was scolded for writing in that particular way. “I had noticed the wrong things,” he writes.
As a parent of an autistic child who has difficulties with verbal communication, I have to ask the question: “whose problem is this anyway?” Certainly I have been dealing with issues, at least issues for me as Adam cannot comment here yet, so I am fully aware that I need to be fair. He has very real sensory and perceptual differences, so I set up a basement full of equipment for him to self-soothe. He has even learned to “self-regulate” by going to read his own books, and I never had to teach him that. His body will completely quiet as he flips through pages of encyclopedias, dictionaries, cookbooks, among many other subjects. He may even appear to layperson as not really paying attention and just flipping pages, but I know it’s more than that. His body-jerking almost always stops, which is how I conclude that he is soothed by his books. I am imagining him looking at those books over and over again, and what he may be gleaning from them. Still, when it comes to getting the responses WE need, he using a “special” reading program at school. Indeed it is really helping with his expressive reading ability, and maybe even with his vocabulary. So I need to let him do both. He needs to learn to respond in a world that doesn’t yet understand the way he learns. He also needs to flip through pages and pages on his own. I can sit beside him sometimes also and talk about the books he is reading. We can type about what he is reading, we can draw stories and make more conclusions or assumptions about what he is reading. When we do things together calmly, we are having lots of fun.
When we teach him a new communication device, it may appear to the person who is teaching that Adam is not focused enough — indeed he appears to be “highly distracted.” On an AAC device (we are still awaiting one from a service-provider here in Toronto) his finger will go to the right picture, letter, or answer, and then he will quickly go to another one to check out what it will do. A keyguard helps him direct his finger more quickly to the correct response. He may have trouble finishing sentences (when he types) and then be reminded to “stay on task.” This is in large part what Facilitated Communication attempts to assist with if done correctly — to remind and assist with the focus. To a person who cannot detect that Adam was about to give the “right” answer (or rather the answer that was requested of him), he would receive a failing grade. Adam is very young and I believe he is not given the benefit of the doubt enough, although his team members are good with this.
It is only fair to say that we do not KNOW everything he knows. We do not fully understand how he takes all this knowledge in and we are the ones that deem his versions of knowledge as irrelevant. We have not developed sufficient ways to measure his responses or his way of learning and seeing, except for the ways we measure responses and knowledge from people who are not autistic. This brings me back to the old ABA adage, “if we can measure it, we can deal with it.” Unfortunately, the way we have historically dealt with autism is by eliminating the behaviours and learning patterns that are essential to an autistic person’s existence. Perhaps continuing to fund this research more heavily is important because as we understand how autistic people learn, we can not only develop better learning tools, but come to better appreciate our children.
Trying to understand this is a first step. As Adam’s parent, I see many of the so-called “issues” being mine, and yes, I become just as frustrated as many other parents out there. It’s really hard to see Adam in distress and it’s even harder to always be guessing what may be causing anxiety or body-jerking (Lack of calcium? Trouble at school? New self-awareness of difference? Trouble with transitioning from task to task? Lack of sleep? Seizures? A very long winter? Lack of exercise? Another neurological issue?…The guess work list is too long). Since Adam appears to be in discomfort since late last fall, I am really working hard at figuring this out (wait-lists are long here in Toronto). Sleep issues, anxiety issues — I know when I have a level head, there is more that I can do for him to ease the situation. We need science now to figure out many of our questions.
Sometimes it feels that makeshift solutions only lead to more issues. Sure, we all want things to be a little easier, but Adam requires more consideration in order to achieve that balance between helping him through discomfort as well as accommodating his needs. As I have been through a difficult year, like many of you out there, I completely understand the reasoning, but I have to keep a level head and look at what Adam has also gone through with a “broken” family. I have needed my sleep, but if Adam cannot, I have to find safe ways of letting him stay up until his body will sleep naturally. I know what I’m saying isn’t easy and there are still days I will resort to the Melatonin, even though, because of the guesswork involved, it pains me to do so. Yet I also know it’s important to stop and slow down and think about how Adam feels and perceives. When I do, everything seems a little easier. As a parent, I can even become proud of myself (it’s important) that I’ve not only managed well, but have helped Adam out too. We are still on that path to finding out if we can help Adam, but I am always wondering excessively about how I perceive the “problem.”
I’m interested in what people in science think about this Perception study. I think we have to spend a lot more time imagining what it feels like to be in Wonderland.
——-
Excerpts from:
“Extraordinary Perception” by Wray Herbert in March/April 2010 issue of Scientific American Mind, pp. 68-69.
Further Reading:
Selective Attention and Perceptual Load in Autism Spectrum Disorder, Anna Remington, John Swettenham, Ruth Campbell and Mike Coleman in Psychological Science (in press). Published online October 14, 2009. www3.interscience.wiley.com





ESTÉE KLAR
TORONTO, ONTARIO, CANADA
Writer/Curator/Founder of The Autism Acceptance Project. Lecturer on autism & the media, and parenting. Graduate student Critical Disability Studies, York University. I like to write about our journey, musings, attitudes towards autism.











That seems to be the big question: How are our biases shaping how we perceive our children’s experiences?
It seems many scientists aren’t prepared to question their own biases, and that’s rather frustrating for those of us who need the answers science can provide. It’s always good to see researchers who are ready and willing to question the assumptions of the status quo. We need more of that before we’re going to answers we can use.
Ludovicus Carolus was if nothing else an interesting mathematician and philosopher.
I have cited the annotated Jabberwocky in the context of linguistic conundrications as he is one of the more inventive users of English.
I don’t suppose you have ever heard of hemisomatagnosia, but it is a condition where the perception is that one side of you is bigger than the other, something which appears to be part of my migraine aura phenomenon.
You don’t necessarily have to be autistic to have a non standard neurology, mine is maybe twice or three times exceptional, I would still be different even if I weren’t autistic, and in some way the later discovery of migraine aura as an explanation for so many perceptual phenomena was a much greater and more significant revalation than autism if you can believe that
Good point, L.R. I say this on a particularly bad body spasming day for Adam. I want to find out what THAT is.
I see no objection to melatonin to aid sleep. I take it whenever I think I’m going to need to get to sleep soon, as when I have an early appointment in the morning. I have Amitriptyline and Lorazepam, but I prefer the melatonin, as it doesn’t leave me feeling drugged in the morning. I don’t know of any bad side effects.
My favorite version of “Jabberwocky” is the translation into Yiddish by Raphael Finkel: http://www.cs.uky.edu/~raphael/yiddish/jabber.html
“Calloo! Callay! O frabjous day!’ becomes (in transliteration) “Calloo! Callois! A yom-tov grois!”
Delicious culture-meld :-).
I know some has been written on Melatonin. It just so happens Adam had his worst spasming day yesterday. I’m not sure if he’s deficient in Calcium or Magnesium or of course I’m concerned it’s a side effect of Melantonin.
It has been Adam’s first week in his new house (not even a full week). Yesterday was also his first weekend. Adam doesn’t tantrum. He hasn’t cried all that much. I’m also wondering if this is an effect of transition.
Last night he spent the night with this dad who has moved back into our old house and Adam was awake all night. You see? Maybe Adam is completely confused right now.
But the spasms are frightening because he can’t even hold a cup of juice without spilling it.
I love my little Autie. I love everything he is. This stuff just started last December and it has been on and off. I don’t see autism as the problem — it’s this stuff that’s particularly difficult. And how much of this is because of all the changes in his life? Or are they new organic issues?
I have also wondered about the effects of Melatonin—Charlie actually fell asleep without it tonight. He does this about once every one or two weeks and I like knowing sometimes he just does not need it.
Regarding Adam being confused with so many moves and transitions and the back and forth between houses (and his old house too)—having resettled in our old house fairly recently, I would say that Charlie was initially fine with this, and then had a long transition period. Adam’s had so much to deal with—it often takes Charlie weeks, months, to adjust to things. He is, like Adam, very sensitive to everything around him and often, when there aren’t the words yet, the communication comes through the body (in Charlie’s case).
Thank you for the Alice in Wonderland analogy. I think it is one to keep pondering.
My father relayed to me a story tonight of when he had moved several times as a child, he would keep exploring. He would sleep as a child for only 4 hours a night. It used to drive his mother nuts (in addition to finding every nook and cranny of the house and going into it). This is just like Adam. Also, looking for tight dark spaces, deep pressure, climbing into drawers and under beds seems to me that Adam is speaking volumes — he is asking for security. I have to admit this weekend surprised me after he was so happy mid-last week. It was the most difficult weekend yet in terms of spasming. I have to be prudent to get tests done so I can rest my mind that this is not organic. If it is, then I will at least know what to do.
I tend to believe this is transitional stress and it amazes me how adults forget how difficult this is for little children — including me, I think. Then I remember how hard the year has been for me and want to smack my head — what am I thinking?! Of course this is dawning on Adam now in a HUGE way.
It seems that he loves his new home. But also he is dealing with change. Excitement and distress are happening at the same time here.
Thanks for your comment, Kristina. It’s hard to wait for the answers.
My son is also 8, almost 9, and he has been “off” for the past couple of months, and over the years, I have noticed that this time of year is ALWAYS a difficult one for him…..I wonder if Adam is responding to the weather in any way? I myself struggle with the “winter blues” and I often wonder if that is why my son always seems to have his worst behaviours January to March…..I have absolutely no scientific evidence to back me up…..but I can say that anectdotally when ever my son has his worst episodes of behaviour you can bet that a full moon is right aroudn the corner, so I wonder if the seasons also have an effect….sounds crazy, but it makes me go “hmmmmmmm”
It could also be a trigger. But he makes noises that sound like choking now and this is new. I will not rest until I at least have his tests done.
I so feel its about understanding our different strengths and weaknesses, we often can do complex things like the Rubik cube, but easy tasks can frustrate us often becoming an irrelevance…. we have our own way of doing things, interrupting the world, a different sort of intelligence in a way different but the same, let me explain for non spectrum minds from north to south, spectrum minds often from North/east to south west.!
I find this fascinating as I have just stumbled across this blog, but only earlier I was discussing whether my complete lack of ability to judge distance, time or size with friends was a by product of my autism. I think some further reading might be in order for me!
- sambennetts.com
Sam, your blog looks very interesting too!
[...] Alice in Wonderland in an attempt to catch up on all of those wonderful movies out there. I wrote about Carroll and his autism here. I have come home to receive a “love letter” from my son and then to coincidentally read [...]