Last week I was surfing the Internet and came across a headline proclaiming autism and circumcision are linked. I couldn’t help myself. I laughed out loud.
In no certain order, I have read the following explanations for autism over the years:
Autism is caused by mercury.
Autism is caused by lead.
Autism begins with poor maternal bonding.
Certain pesticides may trigger autism.
Plastics.
Gluten aggravates autism spectrum disorder.
People with autism should eat more strawberries.
Too much automotive exhaust is a leading cause of autism.
Chemicals found on non-stick cookware may trigger autism.
The one about maternal bonding is sort of painful for me. The truth is, I did have a hard time bonding with infant Jack. The little guy shrieked and whined and cried for a solid year. He started sleeping through the night at six weeks, and stopped at three months.
I was exhausted, and Joe and I were fighting constantly; bickering and arguing and long screaming matches. For the first time, I could feel my marriage slipping away from me like sand through my fingers.
And my first child, Joey—sweet, uncomplicated, good-natured Joey—was a year old at the time. His easy nature only highlighted his new brother’s fussiness.
But I am certain there is no one on earth more bonded to this boy now, and guess what? He still has autism.
I am happy to announce that I do know what caused Jack’s autism, and without further ado, I’d like to tell you.
Wait for it.
It’s kind of a big deal.
Drum roll, please.
Jack has autism because, as his 5-year old brother Henry says, he was bornd-ed with it.
Yes, I believe autism is a genetic condition. I believe that somehow Joe’s DNA mixed up with my DNA and together we had a child who thinks Wednesday is orange. Perhaps his unique genetic coding makes him more sensitive to things in our environment like lead and mercury and plastic.
I don’t know about the strawberry thing though.
(For years I blamed Joe’s side of the family for the autism gene. But a few years ago I went to a funeral for someone on my side of the family, and I looked around the room and was all like hmmmmm.)
I was in a coffee shop last week and a woman came up and introduced herself to me. She said her daughter, Lily, is in Jack’s fifth grade class. I nodded and smiled, took my cup of coffee—ok, ok, and my cupcake—from the counter and turned to leave.
“Wait,” she touched my arm. “I just wanted to tell you something. Lily told me that a boy called Jack weird the other day in class.”
I cringed. “Oh, well, yes. That happens.”
“Lily said she told the boy that Jack isn’t weird. She told him he’s exactly the way he’s supposed to be.”
You can see my dilemma. If I start running around declaring autism an epidemic and screeching about how we need to find out where it’s coming from and who started it and how to cure it, well, that sort of contradicts the whole message of acceptance and tolerance and open-mindedness.
This fragile glass house we’ve been working so hard to build over the past decade will explode into a thousand tiny pieces.
But on the other hand, it sort of is an epidemic. Other families are going to have babies and maybe they would like to have some idea of how to prevent this tricky spectrum disorder from striking. My own children will have their children, and if autism is indeed caused by automotive exhaust, it would be good to know so we could all buy electric cars.
At the same time, I don’t want to focus so much on the what and when and where and how that I forget about the who.
Because I don’t care where it came from.
But I am kind of curious.
It doesn’t matter to me why Jack has autism.
But it might be good information to have.
There’s nothing wrong with him.
Maybe there’s a little something wrong with him because he just spent the last forty-five minutes talking about all the different kinds of gum that Wal-Mart sells.
I wouldn’t change a thing.
I might change a few things.
I celebrate autism and all of its spectacular wonder.
I hate autism because it makes my son talk about gum and Wal-Mart so much.
He is broken.
He is whole.
Autism is no one’s fault.
Maybe I should stop using Tupperware and make him eat strawberries even though he hates them and re-paint the house to make sure there is no lead on the walls or the windowsills.
Maybe I should throw away our frying pan.
Maybe I should have loved him harder, deeper, more when he was a tiny swaddled baby squirming in my arms.
Maybe this is my fault.
As you can see, my feelings about Jack’s autism diagnosis are as complicated as a prism with a thousand colors and angles and light. Some days, my doubts are soft whispers within my heart, other times it’s as though someone is shouting in my ear.
I am not a scientist. I am not smart enough for that. But I am a mother. And although I am not really smart enough for that either, I do know autism from that angle. I know the rigidity and the obsessiveness and the rage over having an aide in school. I know the disappointment and the fear. I know the quiet longing that comes with being different or weird, because I see it every single day.
When you live with someone who has autism, you say the phrase for now a lot.
For now, the radio is on the right station.
For now, he’s not screaming.
For now, he’s sleeping.
For now, he’s safe.
So, for now, I’m going to believe Jack’s autism is because of DNA and RNA and heredity.
For now, I will try to add broad splashes of green and blue and purple and orange to science’s black and white brush strokes. Together, we will fill in autism’s canvas until a clearer picture comes forward.
I don’t know exactly what that picture looks like yet, but I like to imagine it is a utopia of sorts; the perfect intersection of science and people. There are strawberries and puppies and lots of peppermint gum in Wal-Mart, the kind in the blue container.
There are tall, blonde girls named Lily and boys with glasses named Jack.
And if you look hard enough, you can see a glass house in the distance—almost on the horizon. It glints and sparkles in the sunlight, and it is breathtaking.
If you look closer, you will see a sentence etched into the front door. This one sentence—this collection of eight words—well, they are very, very big.
They are a shored wall against a flood of uncertainty.
They are a million bright stars in an otherwise long, dark night.
They are peace and forgiveness, power and pride. They are everlasting absolution.
The first time I heard them, I was in a coffee shop buying a cupcake.
“He’s exactly the way he’s supposed to be.”

Carrie is a Mother of five, wife to Joe, blogger and author of a memoir about parenthood and autism called “What Color is Monday?”
Carrie is also part of the Huffington Post Blogger Team.
Love it! I work in Special Education Dept. I will share this today with my teachers who already know that these children are “exactly who they are supposed to be”. May I confess these children are secretly our favorites!
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Thank you, Jacqueline 🙂
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I want to slap people, who blame anything on Autism. Sometimes I think that people find it easier to blame something or anything and go around screaming “It’s all something else’s fault” rather than just suck it up and go “They’ve got it, let’s take the next step”.
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Amazing post!! I absolutely love it. I work with wonderful families like yours everyday. Some feel as you do and some are far, far away from that idea. I’ve learned from experience that parents must find their own way on this journey. Some may never find it. But in any case the rest of us can certainly believe children with autism are exactly as they are supposed to be. Thank you for the beautiful post. 🙂
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Reblogged this on The Militant Negro™.
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My older daughter has been diagnosed the Asperger’s syndrome as an adult. When she was little, this diagnosis did not exist. As a child, she was thought to be slow in school. I fought this concept because at an early age, she could watch complicated movies with full comprehension and recall. I would read to her books and she would quickly memorize them and then with total recall, play out the different parts. Her favorite story was the Hobbit. This is sad to say but fortunately, she was also significantly hearing impaired. I became her advocate. The school personnel did not need me to say who I was when I called because they instantly recognized my voice.This hearing disability allowed me to find her the help within the school system such as language development therapy. I loved her as is and just made sure she always had a circle of friends to allow her to have social interaction. Eventually, I took time off a successful career to spend the quality time with her that she needed. I tutored her myself. Pretty soon, she was earning great grades and she began to realize that she was actually smart. I enrolled her in a local theater program for years. Here she found success. It was fun for her. She memorized and played her parts well but she also was learning social skills. I signed her up for the Dale Carnegie program so that she could become comfortable speaking in front of people. She was a teenager in a class of adults who were very supportive. For her middle school years, I placed her in a private school where the teacher student ratio was 1 to 10. I made sue she participated in various activities which were fun for her. She attended a local high school which specialized in the arts and she graduated as a Florida academic scholar. Then she received almost a full scholarship to a top rated college and she graduated with a GPA over 3.0.
No, it has not been easy for her. There are always those who cannot tolerate those who act differently. I have told her that those are the ones with a disability. She is such a decent, honorable, kind, hardworking, reliable, honest, loyal family member, friend and employee that anyone is fortunate to associate with her except those who are idiots. Unfortunately, there are a lot of idiots out there but fortunately she has had a lot of support throughout her life including a family who just loves her, loyal friends and coworkers. Frankly, she is a fun person whose company I genuinely enjoy. She is someone who I admire tremendously because I know her courage in not giving up. She continues to love learning.
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I forgot to add that the Asperger’s syndrome is a form of autism. I never did worry about how she became to be different. I just helped her to be the wonderful person she has become.
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Hi Gronda,
Thank you so much for sharing from your own experiences.
Much appreciated.
Best, Mike.
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We are all God’s children and he loves us all.
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God bless him Henry is a genius!
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Oh how I liked this post……………just saying
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May God Blesses..
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Thanks for your lovely post. I think a world where Wednesdays are orange would be pretty wonderful.
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no matter how we try to find perfection in this world, we can’t. And that is because everything is the way it is supposed to be. Everything that is not perfect in ones mind, is perfectly perfect in somebody else’s.
The truth is – even if we find what caused something, we can’t change a thing as today is the only day that matters. We can’t change our past and we can’t predict our future. We can only live today, right here, right now.
The best we can do is – love and go with the flow of life because that is how it is supposed to be. Right answers come at the right time. Right choices are made with the given information and those are the best choices we could have made.
We can’t waste our lives by trying to play “what if” scenarios in our heads.
Your post made me smile!
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