This Is What I Imagine Autism Feels Like for My Son
Editor’s note: This is written by a mother from the perspective of her son.
Anyway, my mom and dad picked us all up from school at 12:14 on Tuesday afternoon. I was in science, and I was surprised when I heard my name on the loudspeaker. When I got in the car, they told my three brothers and my sister and me that we were going for a flu shot. We were all very mad about that.
Then they pulled the car over and said, “Why don’t we go to Disney instead?”
I didn’t know what to think about it. I was happy, but I also like to know about things a long time before they happen so I can think and talk and plan for them.
We got to Disney around 6 at night, and the first thing I did as soon as we got to our hotel was unwrap the soap in the bathroom. I do this every time we go to a hotel. While everyone else is bouncing on the beds and wheeling the suitcases around, I go quietly into each bathroom and find the soap.
We had dinner in a crowded restaurant. I could tell everyone around me was happy-happy-happy, but I could not stop worrying about school. I was worried about missing something fun like a movie during class, and I kept asking my mother over and over to email my teacher.
There was a man sitting right behind me, and he was laughing so hard and weird it sounded like a donkey who had just heard the funniest joke ever. Then my father ordered something pink and spiny called crab legs, and their fishy smell bothered me. And there was a woman at the table next to us who was wearing a string of Christmas lights around her neck, and they were blinking on and off over and over again.
All of a sudden, my brain could barely breathe. It was already 9:23 p.m., and I really like to be in bed by 8:30 p.m., and because of this laughing and the blinking and the smelling, I felt like my skin was trying to come off of my face.
I tried doing my newest trick, which is making my fingers dance and twitch in front of me. It makes me feel good, but I can tell it does not make my mom feel good, because she leaned over and asked me to stop. She said we should have brought my stress ball, and if I had known about the trip, I would have reminded her a lot of times to pack it.
So I tried to keep my hands still, but I felt like a balloon that was going to pop. I had to do something, so I shouted, “What the F*&%!” I know these words are bad, but sometimes they feel so good to say. They feel hot and salty on my tongue, and when I shout them, it’s like letting a little bit of air out of the balloon.
In Disney we went to visit places called parks every day, except they look nothing like regular parks that have slides and stuff. These places are huge and crowded, and they have music and food and people called characters wandering around in their big silly costumes.
The minute we stepped into the park everyone — especially my brothers and sister — started to be so bossy about me. It was making me really mad.
“Jack! Over here!”
“Jack, stay with us!”
Finally I screamed, “Everyone stop bossing me!”
Mom took me aside and told me our family just wants to make sure I’m safe and that I don’t wander off, but it still didn’t feel good. I am 11, not a baby.
The ride called Space Mountain was so fun. My dad took me and my brother Charlie back to the park until late one night, and we rode it all together, and it made me so happy. I could not stop talking about it.
Sometimes I can’t stop thinking or talking about things, like that night at dinner I kept asking and talking about the death penalty because I saw something about it on the television at the airport. Whatever I am thinking about gets big and huge in my mind, and it pushes everything else to the side, like an elephant in a crowded elevator.
My mom got a little mad and said, “Jack! We are in Disney! Please stop talking about the death penalty.”
The next day we went to a place called Epcot, which was totally boring and not as fun as the park called the Magic Kingdom because it was all about learning.
We were on line to go on a ride inside of this big ball that looks just like one of the golf balls my dad keeps in the garage but he tells us not to fool with, and I turned to my mom and asked when it was going to snow at home.
The lady in line behind us heard me, and she said, “Oh, you said it! You said that nasty word, snow!”
I had to double-check because I didn’t think snow was was a nasty word. Snow is nice. It is cold and pretty and sometimes we don’t have to go to school if we get a lot of it.
“Snow is not nasty. You are freaking wrong.”
When I said this to her, the smile disappeared from her face like someone had wiped it away with a sponge. My mom put her arms around my shoulders and turned me away, and then she turned back to the lady and said a few things quietly. I think she was telling them about my autism.
I used to hate when she did this because it made me feel bad. But my mom tells me a lot that autism is not a secret — it is not something to feel embarrassed or ashamed of, because it is as much a part of me as the freckle on my left leg.
World, all day long you flash and dance around me being your funny, stinky, noisy, happy, scary self. You confuse me.
See, I am like a fish inside an aquarium. I want to watch you from behind the glass. I want to stay in my school and eat my regular food and listen to my favorite radio station and go to bed at my normal time. I do not like surprise trips.
I am safe here, in my bubble. Your sounds are muted and hushed, and I can tell the difference between a nasty word and a nice word. I don’t have to listen to your big loud donkey laughs or shut my eyes against your blinking lights.
At Disney we took something called a shuttle a lot. One night we were riding the shuttle late. It was very dark inside, and I was sitting next to my mom and thinking about snow and nice words and nasty words, and then I remembered another word I didn’t know.
“Mom. What does for loner mean.”
“Well, it means, like, to be a alone. A person who is alone. Why are you asking? Do you think you’re a loner?”
“Without you. For yes.”
I could not see her face, but I could feel her wearing her sadness on her body like an itchy sweater, the kind she makes us wear for our Christmas picture. I put my head on her shoulder and then she put her head on my head, and we stayed that way until the shuttle stopped, even though I don’t usually like to touch people for that long.
On our second to last day, we had lunch in an African restaurant called Sanaa, where we could look out the window while we ate and watch giraffes and ostriches strolling around. Our server was a nice smiley man named Boylson. His nametag said he came from Botswana, which is in Africa, and he didn’t get mad when I shouted, “This food. Makes no sense to me.”
After we were done eating this funny bread called naan and my brothers and sister wandered away from the table to look at the animals, I heard my mother ask Boylson if they had autism in Botswana.
She is not shy, my mom.
“Oh yes,” he smiled at her. It was not a real smile that made his face look happy, but more like he stretched the corners of his mouth. “It is everywhere.”
Then she asked about services, and evaluations, and doctors, and he just looked at her and smiled once more, gentle-like this time.
“You know, there was a boy in our village who could not hear a single sound. Nothing at all. But still, we found a way to talk to him. We loved him.”
I was thinking hard about a boy who could not hear a single sound, because I think that would be weird and also maybe kind of nice not to have to hear loud donkey laughs, but when I looked at my mother I could tell she wasn’t thinking about that boy at all. I could tell she was thinking about me.
She was thinking about always trying to find new ways to talk to me, and to hear me, and to love me — to nudge me out of my fish tank and into the wide, open world. She knows I don’t want to be a loner.
I think I know the answer, world.
You and I, we can’t be something or someone we’re not. We can’t change all the way for each other. But this does not mean we won’t be friends.
So I think you should keep being your stinky, funny, loud, busy self. Tell your jokes and laugh your laughs and smell your smells.
And I will continue to be myself. I will do my double-checking and try to understand your words and shrink the elephant in my brain so he’s smaller, more like a turtle.
In the meantime, if you happen to notice a boy standing in the airport and his fingers are dancing in front of his eyes, be kind.
I am trying.
Follow this journey on Carriecariello.com.
The Mighty is asking the following: What’s one thing people might not know about your experience with disability, disease or illness, and what would you say to teach them? If you’d like to participate, please send a blog post to firstname.lastname@example.org. Please include a photo for the piece, a photo of yourself and 1-2 sentence bio. Check out our Share Your Story page for more about our submission guidelines.