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The Problem with Pain: Sensory Processing Disorder

The Problem with Pain

Sensory processing disorder can lead to dangerous situations.

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            Long before my son was diagnosed with Autism, we knew he struggled with sensory processing issues. Sensory Processing Disorder (SPD) affects many neurodivergent thinkers. Sometimes those sensory issues may be inconvenient or draw attention. This week I was reminded of why SPD can be scary. Like many SPD “sensory seekers”, my son does not process pain the way other people do.

“That Tickles!”

            This weekend, my son went skating for the first time. I got a call from one of the adults in the group not long after they started skating. They said my son had fallen several times and hurt his wrist, but he didn’t seem to be in too much pain. He ended up staying for the next hour playing arcade games (since skating was obviously not his thing), and I took him to get his wrist checked after they got back.

            The look of confusion on the nurse’s face was obvious. She began to move his wrist, and he began laughing.

            “That tickles!” he laughed.

The nurse looked back at the X-ray and could see the broken bone. No wonder she was confused. I quickly pointed out that he has sensory processing issues. He doesn’t process pain the same way other kids do. When we saw the orthopedic doctor two days later it was more of the same. He only rated his pain at about a 3 or 4 and laughed when the doctor pressed on the broken bone. Thank goodness the X-rays showed the problem. Otherwise, no one would have taken him seriously.

It’s Scary

            The inability to process pain can lead to some scary situations. For my son, it means he doesn’t always realize when the shower is too hot. He will walk out into an ice storm in his shorts. And, like this weekend, he doesn’t realize when he’s hurt.

            Sure, we’ve found ways to protect him, like keeping the water heater thermostat turned down to control the temperature of the water. When he was younger, I would pick out his clothes for him on extreme weather days. Sometimes making him sit down for a while after hurting himself gave his brain time to process things and realize he was in pain. Often when he does cry from pain it’s because he’s physically bleeding. I suspect the blood is a visual cue that helps him recognize when he’s hurt.

            As a parent, this is scary because I know how important it is to react to pain. God gave us a sense of pain to teach us our limits. Without recognizing when we’re in pain, we only hurt ourselves worse. When my son was a toddler, he touched a hot furnace, but because he didn’t immediately process the feeling of pain, he didn’t remove his finger until he had a significant burn. As he’s grown, he’s had ingrown toenails that he doesn’t seem to notice until they are so bad that the doctor has to cut them out.

            The list of ways this affects my son goes on, and I know many parents who can add their own stories. As a parent, this is the scary side of SPD.

What Can You Do?

Note: The products linked in this section are ones I’ve used or are used by many parents, teachers, and occupational therapists. These are affiliated links, and I may receive some compensation at no cost to you. You can find more information in the Privacy Policy link at the bottom.

            Dawn Sonnier is a local occupational therapist and has worked with sensory seekers in classrooms and in therapeutic settings. She and I combined our knowledge to offer a few ideas for parents and those living and working with those who have low registration or hyposensitivity as part of their SPD and aren’t always aware of pain.

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