Judgey Eyes

Having a son who doesn’t talk puts a big target on my back. Cooper is different and yet he looks like a completely adorable, average boy. And in most cases he is. You would never know by looking at him that he doesn’t say any words. There are a lot of situations where people stare at us. For example, Cooper does a lot of high picture ‘talking’ in all vowels. Often, it is very loud. If we are at Target or wherever he will point and ‘talk’ away. Usually, he will get progressively louder and more animated because we don’t understand what he is saying. People stare. It’s heartbreaking. And I get mad. Mad at Cooper for doing it, made at myself for getting mad and mad at the A-hole staring at us.

I feel that there are 3 reasons why people stare at us when Cooper is have a meltdown (I am sure other moms can relate):

1. They are judging us.

Judging our parenting. Judging me. Judging Cooper. Judging the bag of cookies I am ripping open and giving him just so we can get out of the store. Thanking God they are not dealing with my son. What they don’t know is he can’t talk. He can’t tell me what he wants or why he is mad or frustrated. They don’t know that my husband and I are so worn down sometimes we could just give up and that their stares are crushing to us.

2. They can relate.

All toddlers have meltdowns and tantrums. It’s not just my son. I always make sure to give a nice smile to a fellow mom when they are encountering the dreaded tantrum or whatever. We’ve all been there.

3. They feel bad for me.

This is the worst one for me. I don’t want people to feel bad for me. It’s humiliating. If Cooper acts out in the waiting room at his speech therapy appointments people stare at me and I feel 2 inches big. The receptionist ALWAYS stares at me and it makes me insane. Jamie said I should call her out but that is so not me.

Having a son like Cooper has changed me in so many ways. Too many to list! But I will tell you that it has made me aware of children and their behaviors. And what it is doing to the moms and dads. My heart breaks for them because I know all to well what they are going through.

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Kate Swenson

Kate Swenson lives in Minnesota with her husband Jamie, and four children, Cooper, Sawyer, Harbor and Wynnie. Kate launched Finding Cooper's Voice from her couch while her now 11-year-old son Cooper was being diagnosed with autism. Back then it was a place to write. Today it is a living, thriving community of people who want to not only advocate for autism, but also make the world a better place for individuals with disabilities and their families. Her first book, Forever Boy, will be released, April 5, 2022.

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2 Comments

  1. VeganDee on December 20, 2013 at 10:38 pm

    My mother could relate somewhat to what you describe here. When I was four years old, I was diagnosed with Legg Perthes Disease. I spent the next three years on crutches…. and was instructed by my doctor not to put any weight on my left leg …so that meant: No walking on my left leg. No running, no swimming, no roller skating, no climbing on the playground.

    For three years my mother endured strangers giving us “the eye” because they could not IDENTIFY what was wrong with me. I had two crutches and my left leg was in a sling to keep all the weight off. For three very long years. My left hip eventually repaired itself. So mission was accomplished.

    I will tell you that my mild-mannered 25 year old Mom (at that time) did call out a few people who she felt were judging her (and me).

    Folks need to be aware that they are staring…. have some courtesy, folks. One day you may be on the wrong end of a stare. No fun. No fun, indeed.



  2. Diagnosing Apraxia | findingcoopersvoice on January 9, 2014 at 2:26 pm

    […] break. Secondly, and most important, we had no pressure in our lives. No expectations and no judgey eyes. We spent our days playing and having fun. I played more trains and did more puzzles than I ever […]