I Had the Son Who Bit the Teacher

I had the son who bit the teacher. 

I had the son who couldn’t wait in line at the zoo, or sit through a meal in a restaurant, or play tag during recess. 

I had the son who slept fitfully and woke at dawn.

I had the son people stared at in the grocery store.

I had the son with autism.

We left parties early. We declined invitations to barbecues. We ate our cake quickly. We knew we were on borrowed time. 

I had the boy who freaked out at parades, got lost in the mall, snatched cookies from glass cases, asked people how much they weighed, shrieked when the radio station wasn’t clear, and destroyed every room he entered. 

He only ate chicken fingers, pancakes, cheeseburgers, or popcorn.

In the first grade, he was crushed by anxiety. All at once, his life was ruled by the iron fist of fear.

He chanted about painting babies blue, and worried about spiders in the bookcase, and repeated nonsensical lyrics only he understood.

He rubbed at a spot behind his ear until it bled.

He picked his cuticles until they were raw.

He pulled his teeth out long before they were loose enough.

Around age nine, obsessive compulsive disorder seeped in like water in a basement. 

He washed his hands. 

He checked the clock.

He filled the sink with ice.

I’d see other boys his age on the street or bouncing a ball, their face and limbs relaxed and easy, and my heart would squeeze tight.

I had to believe in him when no one else did.

When he was in sixth grade I had to walk down the longest hallways, with important people holding walkie-talkies and the words clear the room and realize they were talking about my son. 

I walked into the room, the floor littered with books, and collected my tearstained boy from the floor.

I walked to him slowly, as if he was a rare delicate bird who would fly off into the clouds if I moved too fast. When I got close, he stood up and I folded him in my mother-wings, careful, so careful, not to wrap too tight.

He laid his head on my shoulder and we swayed together lightly like leaves in the soft breeze. He wept. I wept, too. Because of him and for him and with him.

Through it all, there was a steady vibration growing beneath my ribcage—a tympani drumming to the beat of three syllables, one word: forever. 

Autism is forever. 

My son Jack is nineteen now. 

It’s better. He’s better. It’s not perfect, but we have a little breathing room.

He eats pumpkin pie, spaghetti, tuna fish, steak, popcorn, pancakes, cheeseburgers, and chicken fingers. 

He’s in a college program.

It didn’t come easily, or all at once. 

It was work.

It was timers at the dinner table, wild chases through the store, watching the purple night sky turn itself over to a tangerine sun. 

Finding the right combination of medication to soothe his spirit while putting Band-aids over the sore spots.

Applications, rejections, research. 

Reckless grace, radical mercy, and tender resilience. 

It was the hardest work I have ever known. 

It’s not a perfect success story.

Never, in a million years, did I imagine we’d make it this far. 

Sometimes he can’t figure out the social dynamics of friendship.

Sometimes he attacks his cuticles with a vengeance.  

Sometimes I see a tall boy with a ball, and my heart squeezes just the tiniest bit.

We still have a way to go, is what I am trying to say.

But it’s worth it. 

He’s worth it. 

Autism is heartbreak by a thousand papercuts, it’s true.

And when you’re staring into the face of forever, it’s easy to believe the minute where you stand will last a lifetime. 

But oh-so-slowly, one minute turns into moments of possibility, strung together like lights on a ribbon.

You see, autism is a game of short strides. It is a million small steps and tiny decisions and atomic goals. 

One day, you look up and realize all the work, all the hope, all the fear, all the worry is turning into something bigger than you imagined. 

One day, you look up, and the world is aglow.

“Mom. I think I’m going to study broadcasting.”