He made her cry

The little girl’s cries were nearly as loud as Max’s screams. She hid her face in her mother’s leg, sobbing. Her four year old words stung my heart even though she didn’t mean them to. “The little boy is yelling at me. Why is he yelling at me?” I tried to quiet Max but he needed to tell me something.

Except the only way he can is by making loud noises at the top of his lungs. Sometimes he points but today, the bright lights and colors of the mall were just too much for him. “He’s not misbehaving.” I wanted to say “This is just the way he talks.” But where Max’s words come out overloud, mine were caught in the silence of my throat.

I had only wanted to take him out to holiday shop. My oldest daughter, Olivia at my side doing her best to figure out what it was he wanted. She gets him. She doesn’t look at the boy, straining in his stroller to get to whatever it is he needs or wants and think he’s being mean to her. It’s just the way he is and she accepts it.

Sometimes we forget that loud voice that doesn’t form true words can be so very jarring. To be honest, it wasn’t much louder than the ambiance of the Mall; the overhead music paired with the children’s TV show playing in the store, the sounds of screaming children just outside at the inside playground, the people loudly divulging their personal business on cell phones and the store attendants yelling back and forth through the store as they discussed the newest display in which we were fully submerged, knee high in sprawling boxes.

It was chaos plain and simple and Max had had enough.

I tried to hurry and pick out my purchases still listening to the mother console her child while I felt her eyes across the rack shooting daggers at me. “It’s not his fault.” I wanted to say and defensively add, “She’s not even near him.” but I’m new to this diagnosis and for the past three years I’ve sheepishly gone about my business, ushering Max out of stores as quickly as possible, dropping armloads of purchases down on random counters just to relieve myself of the snooty stares from other patrons. I haven’t found my voice yet when I’m out and getting glares of disapproval from people that think my son is just being bad.

I want to shout at them “It’s the florescent lights! It’s the freakish Santa display! It’s the fifty thousand twinkling lights that line every aisle, the loud sounds from motion activated toys, the six dozen TV’s that stretch the entire height of the wall, the whatever overstimulating thing competing with every other overstimulating thing.” But I can’t. I don’t.

I just quietly do my best to placate my son and move away as quickly as possible. Do my best to ignore the haughty looks.

Before I didn’t understand. I thought Max was “a handful” I waited for the day he’d “grow out of it” when I could go to the store and have him be okay in a shopping cart, to ask me for something instead of scream. To walk beside me, hand in hand without being gripped by white terror that he’ll bolt. We stayed at home away from the stares, the rude glares from mother bears who’s child cries because Max is over loud. Away from the danger and over stimulation.

Other than therapy and the grocery store where he allowed himself to be buckled into the rocketship shopping cart, he was effectively house bound. I’m trying to change that.

I shut my eyes, tears pricking behind the lids as I made my way to the counter. Max yelling, reaching to touch the sparkling red and gold Christmas tree just above his head. The arched brow of the checkout girl at a particularly loud and long outburst nearly sent the barely withheld drops over the edge. I’m not comfortable yet saying Max is Autistic in public. I’m not comfortable explaining away his behavior as a disability. I don’t think strangers get the right to invade my privacy because their public phone call is being disturbed by a child trying to cope with excess. I look at my oldest daughter as she tries and fails to talk to her brother. He never looks at her, never responds to her soothing voice as she coos to him, doesn’t turn when she asks for a hug or tries to show him a toy.

She never flinches when he screams long and loud right near her ear showing more patience than 99% of the adults we meet. I hug her as we leave, her present tucked in the bottom of the bag, the one she didn’t notice me buy because she was being a good big sister. I wish there was more I could give her, some way to show how much I appreciate her selflessness.

The mother and the little girl pass us on our way out “Why is he yelling at me?” She wimpers again.

Olivia turns, looks her straight in the eye and says “He’s not yelling at you, that’s just the way he talks.”

The tears return for a different reason. I hold her hand as we leave and think it might not be so hard to find my voice after all.

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17 comments on “He made her cry

  1. Hi, your blog is touching and revealing. I think it takes a lot of courage to get through this. I am a mom of an 11 year old boy with autism. His younger brother gets it too. I would be more than happy to share anything i know with you. my email is janek729@gmail.com
    My blog is everythingisathing.wordpress.com
    A family member that follows my blog and yours recommended yours.
    I am sending you a virtual hug.
    Jane

  2. LeAnn Kahl says:

    A powerful narrative. I felt I was there with you Crystal. For all those parents out there facing this, you are their voice.

  3. oldbirds says:

    You write like a novelist with heart, and courage. It’s no wonder Kim loves you and your family.

  4. Jessica Evans says:

    Crystal- you brought tears to my eyes with this. Your children are all amazing and the love you have for them is so apparent in everything that you do. I wish I could tell you in person, since we’ve never met outside of the strange world that is the internet, that you are a wonderful mom. If there is any Mama who can find a way to make the world a better, easier place for her baby, it is you.

  5. Erin King says:

    Hi! I am a special education teacher, and just came across your blog from a friend. I just wanted to say hang in there! It WILL get better and you are doing an AMAZING job. I’m sure you know this, but this journey is not a sprint. Take your time, learn everything you can, try anything that sounds good to you, and most of all…NEVER stop loving and advocating for Max. He sounds like one wonderful and amazing boy πŸ™‚

  6. Kathy Veloski says:

    Crys, I read your blogg and it made me cry! People can be so rude. If Max had a hearing aid, or braces on his legs or was in a wheel chair , they understand right away and are more carring. But , if someone has a disability you cannot see, or dont understand they can often be crule in thier ignorance. Dont let it get to you. Your right , its not thier business! But if it makes you feel better let em have it, both barrels! He is a beautiful little boy. You take him out and do what you want, he has the right to be out and enjoy the world too and you. And give him hugs and kisses for me and the girls and your other little guy too. Tell them I am proud of them . They will become wonderful, aware carring adults!! I worked with people with all kinds of disablities including Autisim. It can be difficult and stressfull and going out in public can be more so, but it will become less stressfull as time goes on. Love him for what he can do now and keep teaching him. He can and will make progress and learn more and more as he grows. Never ever give up. He will teach you as well. Dont be afraid to aske for help and remember to take “me” time for you and hubby. Love you all!!! Aunt Kathy

  7. I admire you so much for not taking the easy way out by never taking Max out in public. It takes courage, I know, to deal with the stares and lack of understanding from others. You’re a great mom. And I can’t even begin to tell you how much I admire your daughter. What a treasure! My thoughts are with you.

  8. I feel where you are coming from Crystal. We have exactly the same with our son. The looks you get from people when he is crying and shouting, trying to tell you what he wants. I found my voice, it was always there with me, I am outstpoken in instances like that, but when you say something people just give you a big mouth back.
    The worst one we hear a lot from adults as well as kids is … Jesus, he sounds like a damn fire truck. If it was not accompanied by a roll of the eyes I would wake away from it.

    I heard a great description the other day of people with Autism.The are parked diagonally across a parallel universe. I’m going to use that next time people look at me.

    As your Aunt says, we never give up.

    • Hi Alex! I’m working on getting some cards made with information on Autism so that when I just can’t take the time to explain or I don’t want to go into it, I can just hand someone a card which will also say something along the lines of “your patience and understanding is appreciated…”

      I like that description, too. I’ll have to remember it.

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