Sensing Something Different

Image credit: Photo by
Thomas Hawk
on Flickr
Licensed under Creative Commons

I was feeling blah this morning and wondering what to write about when I read on Marla's blog that it's Sensory Processing Disorder (SPD) Awareness Month. If you are like our family, every month is SPD awareness month. In fact, we are actually so aware that we do even better than that: every moment of our day is SPD awareness moment! Of course, some of you are wondering what it is that we're so very aware of.

Most of you will remember learning about the five senses (taste, touch, smell, sight and hearing), but do you know what the most important sense organ in your body is? Your brain. For example, I just took a sip of hot tea from a shiny red mug and each sensory input -- from the soft scent of chamomile to the glint of light off the mug to the way the tea burned my tongue (which is still tingling a little now) to the taste of the tea to the firm sound of ceramic mug being placed on wooden table-- had to be processed by my brain.

So, what happens when there is no physical problem with my tongue or the nerves in it, but my brain misprocesses that burnt tongue as a tickle instead of pain? Or what if my brain cranks up the wattage on the light and makes that glint of light blinding? Or if it keys in on the smell of chamomile so much that it seems overpowering? If I process that input differently, I'll probably respond in ways that seem unusual. And that's what happens with SPD.

My son's brain processes a lot of his world differently, but he is most sensitive to sound. When Austen was a toddler, he was terrible frightened of anything that was made of plastic and looked like it might make sounds. In short, he was terrified of anything that resembled, um, a toy. He would scream in terror and curl in a ball covering his ears until we removed the offensive object from his sight.

He once received a gift from a relative: a book that had buttons to make noises as you read along with the story. As he tore of the wrapping paper, his hand hit one of the buttons and he shrieked. He clearly felt it was the most horrible trick someone could have played. A book? A nice silent book that made noises?! I had to promise him that I had made the book go away to the other side of the Earth. (I didn't want to tell him that I actually donated it to the library, because I knew we'd never be able to go there again. As it is, we may never be able to visit Nepal. My apologies to the Nepalese.) I've managed to avoid further incidents by pre-opening presents and screening for noise makers, although we were both tricked a year ago by a musical greeting card, a find that (unfortunately) delighted his sister.

What SPD means for Austen is that when he hears the tinny sound of electronic music that seems to delight other children, his brain tells him it's nails on a chalkboard broadcast over stadium loudspeakers. Pure aural torture. And he reacts in a way that seems (to the rest of the world) out of proportion to what they hear, but completely appropriate for the way his brain is processing the sounds.

SPD has a strong genetic component, which explains why I don't wear socks but do wear sunglasses inside. My brain is also on a slightly different setting than the rest of the world. But if you've been reading me for any amount of time, you know that already.


Visit the SPD Foundation's website for more information and an overview of what SPD is and how it is treated.

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5 Comments

  1. Sophie in the Moonlight says:

    You distilled a very complicated disorder into a very simple engineering format. Great job.

    My older son is really sensitive about fabrics. He could never wear those cute little boy shirts with the big patches sewn on the front because the stitching around and the weight of the decoration jarred his skin. That's the only way to say it. It was just an unwelcome, highly disruptive sensation to his skin.

    He's in Cub scouts now and the only way he will wear his cub scout shirt is over another very soft 100% cotton shirt that's been washed 50 times. Oh, yeah, and fabric softener. I have to use the liquid kind and 3 sheets of the dryer kind for each load so that the clothes have a uniform feel to them. His grandma, my husband's mom, has the same sensitivity. I'm really sensitive to light. I seriously cannot drive during the daytime without sunglasses. My eyes close as soon as bright light hits them. So unsafe. Poor kid got it from both sides.

  2. Mary says:

    The J-man's sensory issues seem to be mostly tactile and oral. Right, so eating? Doesn't happen. I know, you have the same issue, but at least you can get some calcium into him! We're now trying that calcium-enriched applesauce, since applesauce is the only non-crispy-crunchy thing he will eat. Also the talking? It doesn't happen either. Plus, the J-man has some serious vestibular things going on, so stairs and heights are a challenge.

    I wish everyone could understand SPD, without everyone having to live with it.

  3. Mama Mara says:

    I carry around an article about sensory overload in my purse. When, say, my 15-year-old gags at the sight of white food and runs screaming from the school picnic, or my 12-year-old tells great-aunt Lucy that she smells like cow poop, I pull out the article to educate the offended. May I print your post to add to my purse knowledge base?

  4. Mary P Jones (MPJ) says:

    Absolutely, Mama Mara. And that's a great idea. I should have something like that for store clerks. The cashiers at the sensory-overload-wonderlands known as Target and the grocery store tend to get the butt end of most of our meltdowns.

  5. melissa says:

    Good post MPJ :)

    It's odd to me how a lot of Owen's sensory sensitivites have traded out recently. He's less averse to textures these days but much more aware and bothered by sounds. He spent the whole time we were at the pumpkin patch covering his ears because he couldn't handle the sound of the corn cannon - a very muffled popping sound hundreds and hundreds of yards away.

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