Dear World, This is What Autism Feels Like
(Editor’s note: I wrote this from Jack’s perspective, based on conversations and observations of him in Disney and in life.)
Dear World,
Last week my family went to Disney. We went to the one in Florida, not California. The one in California is called Disneyland and it opened on July 17th, 1955. Disney World opened in 1971.
Anyway, my mom and dad picked us all up from school at 12:14 on Tuesday afternoon. I was in science and I was very 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.
But this time my mom was all sneaky about it, because she hates when I know about trips. I always want to pack my own suitcase full of the things that make me feel calm inside, like my special bunny and my Chapsticks.
One time we argued for two hours because I tried to pack my humidifier for our skiing trip. I kept showing her how it would fit into the suitcase fine as long as it didn’t have any water in it but after a while she shouted, “We are not taking that humidifier, Jack! Stop driving me so crazy!”
We got to Disney around 6:00 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 e-mail 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 I could smell their fishy smell and it 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 and on and off over and over again.
All of a sudden my brain could barely breathe. It was already 9:23 PM and I really like to be in bed by 8:30 PM 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 very 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.
Words are very weird for me. If they sound even a little bit different I have to double-check in my brain before I recognize them.
Like the way my bus driver likes to say, this is the route home, and she says it like the root on a tree. When I hear her say this, I think of tall, straight trees with soft leaves.
Then one day we had a substitute bus driver and he said we’re going to take the same route home, except he didn’t say it like the tree root, he said it like rowt, so then I had to do my double-checking and figure out what he meant.
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!”
“Where’s Jack?”
“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 am safe and that I don’t wander off, but it still didn’t feel very good. I am eleven, 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 do my double-checking 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. My dad was always shouting, “Come on! We’re going to miss the shuttle!” and then when we got to the pick-up place it would have just left like a second ago so we’d stand around and wait another twenty minutes.
One night we were riding the shuttle very 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.”
“Oh, Jack.”
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.
Be tender.
I am trying.
From,
Jack
Cathy Ballou Mealey
November 23, 2015 @ 12:24 pm
“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.”
Amy G.
November 23, 2015 @ 12:52 pm
Love it. Thank you again.
Kathy
November 23, 2015 @ 2:12 pm
“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.” You said it all Jack…that is all I wish for my son Nick and the world…to be friends.
Jamie
November 23, 2015 @ 2:13 pm
Reading this helps me to understand my own son. Which I know will never really happen fully because he thinks so different than the rest of us. Thanks
Jeannie
November 23, 2015 @ 3:00 pm
Jack, my daughter is 17 (she has Asperger’s) and she would probably say the same thing as you did to the lady about the snow. (But she wouldn’t use the word “freaking,” so it wouldn’t be exactly the same as you said.) Keep on being yourself, Jack. We like hearing about your experiences.
Josii
January 29, 2016 @ 7:54 pm
I am 18,and have Aspergers, and that snow thing is really bothering me… i would of said the same thing.. And I still dont get it :/
Jan
November 23, 2015 @ 4:01 pm
Jack, you put words to things I don’t have words for. Thank you for being yourself and helping me to understand the “Jack” that lives in my house (his name is Brody).
Keri @ Reluctantly Suburban
November 23, 2015 @ 5:02 pm
Thank you.
My words are failing me.
Just thank you.
Christine Duffley
November 23, 2015 @ 6:35 pm
Dear Jack and Carrie, how awesome to read this piece. Jack, you are an excellent writer. I am just like your mom, Jack. Sometimes I just say “Stop” and I wish I had a better way to turn off that thought or feeling for my son, Christopher who is 14 and autistic as well. Thank you for being “real”, funny and helping the world know your world. You are special to the world, never forget… and together we make the world more gentle and loving. Christine Duffley
Sue Davis
November 23, 2015 @ 8:24 pm
What a thoughtful, beautiful post.
Kimberly
November 23, 2015 @ 8:53 pm
Thank you for your words Jack.
Sara
November 23, 2015 @ 9:02 pm
Dear Carrie, you’ve done it again. I’m here in Tokyo, Japan, in my old adopted home which i haven’t visited for 10 years and having an amazing time. Maybe because my heart is already so open because of this wonderful experience i am having, or maybe because of the gifted writer that you are, i’m reading your post with tears streaming down my face. “… we found a way to talk to him. We loved him.” This is my wish for my own dear son, for everyone who suffers, for the entire world – for those around them to find a way to love them.
Kirsty @ My Home Truths
November 23, 2015 @ 9:47 pm
I loved reading this. We took our 11 yo to WDW earlier this year which involved a long haul flight from Australia and weeks away from home. We did a LOT of preparation to get him there and we all ended up having the best time but I could definitely see him in this post. He struggled whenever we dined in particular because of the noise and distractions but he loved the rides which seemed to give him the sensory input he needed to get through it. He wasn’t as much of a fan of Space Mountain – once was enough for him – but he went on the Seven Dwarves Mine Train multiple times and always came away with a smile.
Deb
November 23, 2015 @ 10:51 pm
You always make me cry.
Tammy
November 24, 2015 @ 1:13 am
We went to Disneyland 2 weeks ago for my daughter’s 18th birthday. I prepared so much for Nash, age 10 to enjoy this trip as much as he could. We went 3 years ago when we didn’t really understand all that autism is and how to deal with it and our son. We did better this time. I hate autism so much most days and other days just fascinated by it and how it works…or doesn’t. You always bring an emotion that I can’t feel at the time because if I do…I may not be able to stop. Thanks for your Monday writing.
Gigi
November 24, 2015 @ 7:34 am
Great piece. Have you heard of the Brain supplement, EHT? It helps regular people, like me, who don’t have autism with mental clarity. It helps me focus and I no longer have times when I’m searching for words. It’s botanically based and was discovered by the researchers at Princeton university. It might help you get a different perspective. Email me for more info or go to: http://skincarewonder.buyneriumeht.com/
Autism Mom
November 24, 2015 @ 10:49 am
Beautiful. This is my favorite part: “…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.”
Alexis R.
November 27, 2015 @ 1:25 pm
This is so beautiful. I work in a classroom for severe autism at a middle school, and each and every child has my heart in their hands. They try so hard to fit into the world – but it’s the world who needs to try harder to fit them in. Love and hugs to Jack and your family.
Kristen M.
November 28, 2015 @ 3:03 pm
Thank you Jack. My 8 year old son has HFASD, and I will read this to him. I just know he will identify with most of what you said. It will make him feel better to know that someone else feels the same. Please continue being yourself! You are truly amazing!
hernameishope
November 28, 2015 @ 7:50 pm
This blog post is so full, deep… Thank you for sharing with us a piece of your heart. <3. Take care & God Bless! 🙂
Janet Anderson
November 29, 2015 @ 5:28 pm
Every blog post I read makes me a better person and Jack is such a special person. A gift from God to all of us who share living with the same fears, wondering if our loved one will fit into society. He is perfect in the eyes of God and will always be. Carrie thank you for sharing your family with us and the world. You are a blessing.
Jenn M
November 30, 2015 @ 12:40 am
“I could not see her face, but I could feel her wearing her sadness on her body like an itchy sweater” ~ Carrie, this is my favorite line because Jack describes you exactly as I feel when I’m trying to ‘hide’ behind a happy face but my thoughts for my own ASD son can scare me on the inside
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Veronica
June 29, 2016 @ 9:55 am
Funny – reading this about Jack I see some of myself..I wonder if this Autism isn’t really just an exaggerated Introvert-ism() – I have always retreated from the ‘crazy’ world, never understood why people like all that hoopla & furious ‘goings on’ they do for no apparent reason than because it is ‘something you do’ ! The need for being part of what others are doing..to me is selling your own self for the sake of being accepted by the ‘group’, which I have always resisted. I think the article is wonderful, expressive & helps others to understand this situation some find themselves in. I am 70 and I can remember kids who were ‘different’ when I was at school so it may not be a current dietary thing causing this or vaccines, but maybe we are just recognizing or labelling things differently ?
Anyway, tell Jack he is a lovely person and I wish him the most wonderful life, and just enjoy being who you are…every one of us has something to teach every other one of us. Thank you for the lessons I learnt today from you Jack X