Your Child Has Just Been Diagnosed With Autism

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Dear friend, (whose child has just been diagnosed with autism.)

Your child has just been diagnosed with autism. Maybe it came as a shock. Maybe not.
Maybe like me you already had an idea that something was going on. But you still felt the sting when the words were said out loud.

There are so many things I want to tell you. So many important things that I feel you should know.

But right now, if you were anything like I was 9 years ago, your head is spinning.

You are motivated and paralyzed at the same time. You want to do everything you can as fast as you can to help your son. But you are also hitting a lot of dead ends. It feels like hurry up and wait.

At least it did for me. You feel a bit like you failed your son. You feel scared and worried and angry and sad. You feel it all.
I won’t throw a bunch of stuff at you. Because either you won’t remember it or it will overwhelm you.
I’ll just tell you the really important things.

First, your child is exactly who he is supposed to be.

He’s not different because he has a diagnosis. It wasn’t given to him by a doctor. He is the same amazing kid as he was before the the label was given. Remember that.

Second, let your child show you the way.

He will lead you off the path of ‘typical’ and into his magical world. Go with him. Sit. Listen. Learn.
Just be there with him as he studies the sky and dances to music you cannot hear. Be his shield too. The world doesn’t understand autism yet.
And while you may not yet either, you are now at the forefront of his journey. You will encounter unkindness and fear towards his differences.
The first time it happens it will take your breath away.
And know there is no way to ready yourself for it. But once it happens you will truly understand what advocacy means. And it will give you a strength like you’ve never encountered before. It is a gift to protect these tiny humans.

Third, believe in your child.

Believe in him so much that people think you are crazy. And then believe in him more. You will be told all the things he will never do. The story of his future will be written for him and you.
Rip it up mama. Rip it up and write a new story. Yes, the chapters may be different than every other child you know. His story will be unlike the others. And that’s okay.
It will be just as beautiful and just as profound. No one else can write his future. Remember that. Believe in him.

And lastly, give yourself grace.

A diagnosis of autism can feel scary and different. And it’s okay to say that. But different isn’t necessarily bad. It’s just…different. Go slowly and take it all in.
And love that little one.

Welcome to the club. Look for the helpers mama. We are out here. Whether it’s other mothers like me or autistic adults who can teach us both.

Lean on those who get it. Ask questions and let us help when we can. You are not alone. Not ever.
Signed, a mama who has been there before.
Finding Cooper’s Voice is a safe, humorous, caring and honest place where you can celebrate the unique challenges of parenting a special needs child. Because you’re never alone in the struggles you face. And once you find your people, your allies, your village….all the challenges and struggles will seem just a little bit easier. Welcome to our journey. You can also follow us on Facebook.
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Kate Swenson

Kate Swenson lives in Minnesota with her husband Jamie, and four children, Cooper, Sawyer, Harbor and Wynnie. Kate launched Finding Cooper's Voice from her couch while her now 11-year-old son Cooper was being diagnosed with autism. Back then it was a place to write. Today it is a living, thriving community of people who want to not only advocate for autism, but also make the world a better place for individuals with disabilities and their families. Her first book, Forever Boy, will be released, April 5, 2022.

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