xmlns:og='http://ogp.me/ns#' Yeah. Good Times.: "All Kids Do That" Part 8: Behaviors

Sunday, February 5, 2012

"All Kids Do That" Part 8: Behaviors

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Today's contributor is Linda, who blogs at Outrunning the Storm.

I lost a close friendship after my four year old son, Charlie, was diagnosed with Asperger's Syndrome. Our children had been in the same preschool class together until mine was asked to leave due to growing behavioral problems.

When after nearly a year of struggle we finally received his diagnosis, I shared it with my friend.

Asperger's, I said. At the time, this new word was still bitter in my mouth and every time I heard myself say it out loud, it felt like a punch to my chest, it took my air for a second or two.

But why, she responded, I don't see it.

I wasn't ready yet. I had no words. I stumbled through a string of reasons I did not yet fully understand myself. He has trouble transitioning, he doesn't get social cues, he can't see other people's perspectives.....

That sounds like every four year old I know, she responded, maybe my daughter has Asperger's too.

Yeah, they are all like that, but, it's just that he's ...well....more....

It sounded weak because that's how I felt. Weak and alone and afraid and I needed so much from her in that moment. I just didn't know what yet. So I let our friendship drift apart.

She was right though, the hitting, shoving, and biting other kids, that my three year old was doing at preschool, was in many ways typical behavior for that age. Though he did it much more often than any of the other kids, that was not the entire story of why it is not the same.

Here is the difference. All children will act out in some way as they learn about the world. But, a typically developing child will see the reactions that other kids, teachers, or parents have to these behaviors and learn connections of cause and effect. This doesn't mean they will never do them again, but they are learning to trust their instincts about people and how they can be expected to behave. But, autism, for my son, means he does not see these reactions so he does not learn from this relationship of social cause and effect. To him people's angry reactions and subsequent punishments come completely out of the blue and end up giving him all the more reason to think he needs to fight to defend himself from a confusing and unpredictable world.

There are several reasons why he doesn't see these reactions. He does not recognize facial expressions. So the parental 'look' we are all so used to doing, means nothing to him, he simply doesn't see it. He can not hear the emotional tone in voices, so while a sweet, gentle voice is a preferable sound to him, it implies no different meaning than does an angry, stern tone. Finally, he does not understand that the way he views the world in any given moment is not the same as the way everyone around him sees it. So, if he thinks throwing a toy at someone is funny, then he has no reason to believe that child would see it any differently. By the way, this is called theory of mind, this understanding that everyone has their own unique thoughts and feeling, and some will say it means people with autism lack empathy. Please, please know this has nothing to do with empathy, that is a misconception that is so very hurtful to people on the spectrum and those of us who love them.

At one point, after I had read all the books and thought I understood, at least intellectually what everything I just explained meant, there was a moment with my son that finally brought me true clarity. I think it may have been the first time, in fact, I really saw him and understood what a struggle life must be for him.

We were at a park with his twin brother Tommy and Tommy's wild, raucous friend Kyle. Tommy and Kyle were running around, screaming, chasing each other, and laughing when Tommy began, through fits of giggles screaming, no. no, Kyle stop! He then happily continued to invite Kyle to try and catch him. At this moment, Charlie got up and grabbed Kyle by the shoulders, shoved him to the ground, and sat on his chest. I jumped up and quickly grabbed him off the boy.

What are you doing! I screamed.

Tommy told him to stop and he wouldn't.

I fell to my knees, I got it. That is all he saw. Not the laughter, not the obvious enjoyment in Tommy's voice. Just the words, that's all he had to go on. He was blind to the rest. Just imagine trying to navigate the social world on people's actual words alone.

I have since gotten back in touch with my lost friend. On our neighborhood walks, while the kids are in school, we once again talk about our mutual love of books and food and all the things that make me feel like a whole human being and not just a special needs mom.

But, then I make sure the topic turns to autism and all it means for our family. Because I know, my son will spend his life having to conform to fit in this world but, I have to believe that if I keep sharing his experiences with anyone who will listen then the world may learn to conform a little bit to fit him too.



Comments (21)

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I think my husband and I had a similar realization once we realized how literally our older son took everything. How our emotions and tone really didn't mean anything to him.
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As a member of the Knights of Columbus, a Catholic mens group, we started a "squire" program. It was meant to be a kind of boys club, with us as the mentors. We had events, and fund raisers, it was fun. All us men, working with the boys and bringing them along in the church. One of these boys had Asperger's. I say that now, but at the time, we had no idea. What we all knew was that this boy was "odd". His father is a good man, a good friend, and a member of the Knights as well. At our first outing, basically a sleep over in the school gym, he tried to explain his son. He told us that his son had social problems, and didn't interact with other kids, etc..etc. At the time, we thought that he was making apologies for his son, so we all said, "Sounds like the typical teen". He kept trying to explain, but we just reacted with the same line. I wish I knew then, what I know now, so I could have been there for my friend. Please forgive us NT's, we so often, just don't know.
oh man, they're so literal! words mean all to them & they take them seriously. at least you know your boy has his brother's back!
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I don't know what to say. Some of the above was familiar but not all of it. Hey, but his brother is lucky to have him. I was envisioning the scene and laughing. Adorable. Anyway, just wanted to let yall know I was reading. Good write.
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I think Asperger's is here to teach us how to listen, and in many ways it's surfacing BECAUSE we listen. For generations, people have been demanding conformity from their children in unsympathetic and many times violent ways. For the first time, we're tuning into the struggles of the Aspie. My point is, good for you, Outrunningthestorm, for hearing your child even though you had people saying "all kids do that". For intervening with healthy therapies instead of punishing him. For spreading the word so more people can hear kids like him.

It's very hard to communicate well with an Aspie (I know - I am one). So if we can get Aspies and NTs to understand each other, think of the effect that could have on humanity in general.

P.S. jillsmo - I think your writing voice is adorable. It's a pleasure to read.
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Great post! The explanation about his interpretation of the world (theory of mind) was really enlightening - I mean I kind of knew some of that stuff, but it was spelled out in a clear, understandable way.
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Great explanation. It seems in some ways especially challenging for Aspies who do not necessarily present as the typical world's view of what an autistic person would be like. My cousin with Asperger's is talkative, smart, and funny. But of course, he has challenges too, that he and his family work really hard to manage. My son is further along the spectrum, and non-verbal, so we have our own set of challenges, but, for better or worse, when I say "he's autistic," no one tries to argue that fact. (Though I do still get "but he makes such good eye contact!")
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I love your post. Before our son was diagnosed at age 5, many of our friends tried to shrug off his bad behaviour. We've heard "I don't see it" from lots of people. The reason they don't see it is because they don't want to. And I don't blame them for not wanting to see it.

Our son demonstrates some of the same behaviour that your son does. He has no concept of exaggeration either. Every time someone gets mad or yells, Jacob wants to yell at them back. He too has difficulty in processing other behaviour and feelings. I just hope that our sons get "better" as they age.
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Thanks for posting, I can relate! This was how my son was in pre-school too. But back then the diagnosis was new (or maybe we just live far enough midwest no one here was talking about it yet in late 90s) and no one came to the conclusion. He was just a kid that didn't fit in. I remember my co-workers making comments about what could he possibly be doing to be kicked out of a preschool? All kids have behavior issues. Yeah, it is different but we didn't have a name for it then. Thanks for the post. I hope it helps others see the difference, whether in another kid or maybe even in their own so they can know to get their child evaluated.
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First, nice to newly meet you. I have (6 yo) triplets and two other children. My middle triplet has Aspergers and my First born triplet is starting the testing phase now---although she is barely detectable, other than some academic issues at this point.

Last year, my son peaked under the boys bathroom stall because he heard his friend in there. The friend flipped out and told the teacher and of course my son was horrified and confused and just absolutely beside himself because he just doesn't get what is/not socially acceptable. He has no body modesty and doesn't understand the need for privacy, etc!

The same week, "Jane" told him that she didn't like "Bobby" because "Bobby" was mean. So my son, very matter-of-factly, stood up and announced to the "Bobby" boy that "Jane" thought he was mean. This set off a huge episode of hurt feelings and panic, and betrayed feelings..etc. etc. etc.

I'm not telling you anything you don't already know. People are always stunned when I say my son has Aspergers. They have a hard time "seeing" what I see...or rather...seeing what he does NOT see. But we get it. So we got their backs, no?!
Wow! That is one of the best "all kids do that" responses that I have read. Thank you from the bottom of my heart for writing this. I will definitely be sharing.
Very powerful.

And spot on.
Very enlightening and touching post.
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Melissa Davis's avatar

Melissa Davis · 685 weeks ago

Thank you, love it
Great post...very well articulated. Thanks.
the lack of empathy actually comes from some of the people closest to us--the ones who immediately dismiss before thinking it through. Well said.
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Well put. I know a 13 year old boy who suffers every day from this literal thinking. It, of course, causes all kinds of misunderstandings from his peers. Many people are beginning to understand some things about autism - sensory issues, lack of eye contact, but understanding the literal thinking aspect would go a long way to true understanding.
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I really appreciate the distinction about literalness not being a lack of empathy. One of my best friends has an Aspie son (who is in turn one of my older son's best friends). I've always been confused by the empathy thing: I'd heard that Aspie meant lack of empathy but this kid is one of the most empathetic I know. He's very concerned about treatment of others; he identifies situations in which a child's feelings might be hurt and will discuss in detail how it can be rectified. But it is a spot-on description of him that he doesn't understand that others don't see the world the way he does. I've had conversations with him that are frustrating because it involves trying to clarify another world view and I've listened to his mother's exasperation over this inability to understand where someone else is coming from. Thank you so much for the clarification.
I am so glad I found this blog! My 8 year old son was recently diagnosed with Asperger's by a psychologist. We initially had a diagnosis of ADHD. It was during a visit with my son's wonderful pediatrician, where I told him all of the things that my son was doing, while crying and having a panic attack, that he told me that he might have Asperger's. He started behavior therapy for his social issues and regimented ideas of how games should be played. He has no idea why he gets in trouble in class some times. He has trouble seeing anyone's point of view, he can only see his own. He doesn't understand that his thing about following rules and trying to tell others what to do is why kids don't like him. He would rather be right than get along and have more (or lasting) friends. We have never had play dates and he's very immature. I'm learning how to deal with this and get him the help he needs to be successful. I totally get the "I don't think your son has that" reaction from family members. Denial doesn't make me feel any better. I am actually so relieved that there is something wrong and that we can get him help. I realized after reading "Look Me In the Eye" that my husband clearly has/had Asperger's. He doesn't want to really talk about that. It's a lot of work being an elementary school teacher, mom of two, and having 2 boys in the house with Asperger's. I know parents who have kids with more difficult problems go through more.
2 replies · active 616 weeks ago
just let him read and write. Talking about it is stressful. That's why I blog and read about research and other people's experience. Biggest challenge of late life diagnosis is framing your life till then. We all have stories about ourselves and they need a lot of reworking and re-understanding. Try to learn about the strengths of aspergers. Asperger's as an explanation of all the problems is much harder to accept then a development/learning/communication condition that made us the person we are. With the things we are rightly proud off: the commitments we made, the trust we gave, etc.
your comment about your husband reaction inspired me to give some reflections on my own diagnosis reaction on http://hansaspergerjunior.blogspot.com/

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