Chip off the old block.
The apple doesn’t fall far from the tree.
and my personal favorite, taught to me by a friend:
Cats don’t have dogs.
Because really, they don’t.
All these expressions mean the same thing – our kids are a lot like us.
I’ve written a lot about all the sensory challenges that my son Howie has. But my other two have their sensory “things” too.
As do I.
I’m a clear sensory avoider. I don’t like hugs or being too close to people I don’t know. I’ll be the one to sit across the room on the chair rather than share a comfy couch. I can’t stand it when someone sits right next to me in a movie theater, especially when there are still plenty of open seats. And at a party or gathering, I’ll be the one holding up the wall in the corner, nursing the same drink all night so I don’t lose my spot. That’s just me. And really? Never touch my neck. Or feet. Off limits. I haven’t worn a turtleneck or scarf since I was in grade school, and if I can avoid socks and boots, I’m a happy person.
I have my food issues too. If something doesn’t smell or look right, I can’t eat it. While I am a big fan of food in general, I have some serious texture issues. Like tomatoes. And olives. And a banana that is more than a day ripe. I’m shuddering as I write.
And of course, my fear of failure paralyzes me. I quit softball because I didn’t want to try out. I worked my butt off in school because the thought of a bad grade terrified me. I retreat and read to escape.
My oldest is a lot like that. He likes his personal space, and he likes it quiet. He can’t stand it if his shirt is too tight on his neck. If the house gets too noisy or if someone in his class is clicking their pen, he’s upset. His food needs to look just right or he won’t eat it, and forget about mixing any food together. He’ll play baseball but gets frustrated quickly with team competitive sports. He prefers to play the piano and read. He gets really good grades, but wants more from school than just rote work. He wants it to mean something.
My youngest needs his socks to fit just right and his pajamas to be loose. I used to think that his meltdowns over spilled food were a sensory thing, but we discovered quickly that it was because he was missing out on food.
And my husband…well, this is my post not his. Let’s just say that our two sensory avoiding/perfection seeking trees created some apples that didn’t fall far from us. Or something like that.
It’s clear that somehow our kids got this from us.
Somewhere in the mix, Howie came along as the lone sensory avoider and seeker. He’s the only one with an actual sensory processing disorder diagnosis. And with that also came the autism spectrum diagnosis.
So it was great interest and a knowing smile that I read the essay “Like Mother, Like Son” by Amanda in the book Wit and Wisdom from the Parents of Special Needs Kids (yes, that’s the book I’m in too!). I’ve been a reader of Amanda’s great blog Confessions From HouseholdSix for a while, and was so glad when she agreed to write a post for the SPD Blogger Network on her son’s sensory issues. They received their second autism diagnosis in the their family about a month before we got our second one.
In her essay, she writes:
When I dreamed of what my children would be like, I dreamed they would be like me. They would get good grades in school. They would like to play sports. They would be involved in other academic activities after school as they got older. I never dreamed of the word autism.
Autism has been a funny little word in our house. My oldest son was diagnosed later at age eight and a half. By this point I had realized that this child is me, only more intense. But he is me. Does that put me on the spectrum too? This is a question that my son’s diagnosis has made me ponder often.
She goes on to talk about all the sensory issues that she shares with her son, and they were so familiar. Clothing troubles? Check. Food issues? Check. Desire for perfection? Check.
Her last paragraph sums it up nicely:
Are these all traits of autism? It’s hard to say. Does this mean I’m on the spectrum too? I don’t know. I do know that autism or not, I did get a child like mine.
And this is, of course, what swirls around in my head all the time. Is my oldest on the spectrum too, like his brothers? Are we?
It’s a question that I’m not sure has an answer, nor perhaps does there need to be one. We all know that the spectrum is broad and wide, and that everyone – EVERYONE – has some sensory issues. It’s about how you cope with them. For Howie, he can’t cope with them right now. So we’re teaching him. And in that process, we’re teaching his brothers – and the rest of us – how to cope as well.
I do know that seeing pieces of me in my kids gives me a better understanding of what they are going through, and gives me more patience and tolerance in helping them through the tough moments.
That’s what Amanda’s essay did for me. Seeing myself in her words helped me be a better parent. Just another way that I feel a little less alone in this world.
“As we go down life’s lonesome highway,
Seems the hardest thing to do,
Is to find a friend or two.
That helping hand, someone who understands.
And when you feel you’ve lost your way,
You’ve got someone there to say, “I’ll show you.”
Ooo-oooo.
Say you, say me, say it for always,
Aw, that’s the way it should be.
Say you, say me, say it together, naturally” – Say You, Say Me by Lionel Richie

November 21, 2011 at 10:13 am
You know, it’s funny, the more Nik grows and changes, the more is dad and I can see the parts of us so clearly within him. As you said —intensified, but still part of us. I suspect “the spectrum” is as broad or as narrow as fits the individual’s paradigm. And, in my mind, yes, we are all somewhere along that spectrum.
November 21, 2011 at 10:14 am
Great post! I, too, often wonder if I might be a little bit on the spectrum. I am definitely a sensory avoider…and see similarities between my son’s quirks and mine. I think it is natural to ponder this. Reading your words helps me feel not-so-alone…thank you.
November 21, 2011 at 10:28 am
You have such a great perspective on the boys and yourself.
Sometime it would be fun to share how your apple fell from dad’s and my tree.
November 21, 2011 at 10:38 am
Susan, that *would* be an interesting tale. Do you blog? You should write the story. I’d read it.
November 21, 2011 at 10:39 am
Awesome post! My husband is the sensory avoider in our marriage…he hears white noise that I just tune out like the dishwasher running or the hot water heater or the sump pump for godssakes. I’m with you on the person sitting next to you in the movie theater though…drives me nuts! Just goes to show that not everything we see in our kids is the “autism” talking…they really are our mini-me’s sometimes!
November 21, 2011 at 10:51 am
I’ve long said that Charlotte is a more intense version of myself. I see it all the time. I also think that it’s a very gray area where neurotypical ends and the spectrum begins. I’ve joked before that Charlotte has one foot planted on the spectrum side and one on the NT side. But are there really sides? Everybody has quirks and sensory issues – and, to me, in my opinion, it’s very subjective for when it crosses into disability. For some people. There are some people for whom it’s not gray at all. I don’t know where I’m really going with this other than to say that all your questions are ones I’ve pondered as well.
November 21, 2011 at 11:39 am
I LOVE this post. What great perspective. I’ve never thought that my son is like me in the slightest – but then you wrote above about the movie theatre seats and I’m exactly the same! I practically go bonkers when someone sits to close to me. And don’t even get me started on people who get in your personal space when they are talking to you! I had a woman practically chase me around my driveway this summer because she kept getting in my space and every time I backed up she would just step even closer! This post is certainly food for thought!
November 21, 2011 at 12:16 pm
Right there in the corner of the room with you (a respectful distance away). In fact, you could save the spot for us while I refresh our drinks.
November 21, 2011 at 1:25 pm
I always say that my little guy gets it from me. He hates loud noises and so do I. Yes, not far from the tree at all~
November 21, 2011 at 5:27 pm
I recently wrote a post outlining how my sons autism is no genetic surprise when you look at myself and my husband. We both score highly on the Broad Autism Phenotype test (which you can do online). My daughter is probably the most sensory sensitive out of all of us, and is not ASD. WE are a mixed bag.
November 21, 2011 at 8:05 pm
Interesting and entertaining post!
November 21, 2011 at 8:13 pm
Totally love this post and relate as always. I did the “Out of Sync Child” checklist for myself when I first learned about J’s SPD and was totally blown away, and I understood a lot more about myself. Would love to be in that corner with you and Spectrummy Mummy. No touching and limited eye contact from me, but I’d love the company of people who get me. Thanks for another fabulous post!!
November 21, 2011 at 11:04 pm
Great post! I see so much of me in my kids too. I have huge sensory issues, learning issues and yes, a good fear of failure, yet I’m not on the spectrum myself. My husband is the same way. My poor kids just got some strong genes from both sides of the family tree so their symptoms are so much more intense.
November 22, 2011 at 6:14 am
I’m glad you could connect with what I wrote. I’ve not found many parents who looked at their child’s needs as things they have themselves. The more we delve into the boys’ diagnoses, the more I see it – in both of them. I’d be totally lying if I said i didn’t get anything out of my 5yo’s OT appointments myself. I like playing in the beans and beads with him. I like the tunnel. I like the putty and dough (even if he doesn’t). The big difference is I’m an auditory avoider, and my boys are seekers. I’ve really thought about getting myself a paid of the earphones I’ve seen some kids wear to block out the noise, because they can get quite loud.
November 27, 2011 at 10:48 pm
I have been telling my husband that I have a touch of autism for years now. I definitely have major sensory issues and my kids seem to have inherited all of them. Poor kids….