The Future Of Autism

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When my son’s autism was discovered at age three, I focused on the present. I dove into getting him all the help he needed. And our family too.

When he was six, I started to think about the future. About forever. But I wasn’t ready yet. And many people told me not to think about it. They told me to wait. To take it day by day.

Now that he’s nine, almost double digits, I can see the future with some sort of accuracy. I like to say we all settled into autism. Him and our family.

And while his future, our future, looks different than most, I see unbelievable beauty too. I see hope. I see faith. I see a wonderful life. I see a family who treasures a boy and the gifts he brings to the world.

But there are also parts I hadn’t thought of. Parts of development that most people take for granted. Parts that are still hard for me to see.

Sometimes they take my breath away. Like a sneaky punch to the side. They come out of nowhere.

I didn’t know he’d get so big and so strong.

I didn’t know I’d have to place my hands over his and wash his hair.

I didn’t know he’d always need someone to hold his hand.

I didn’t know he wouldn’t be able to communicate pain to me. And that often, he would self-inflict it. No one prepared me for that.

I didn’t know he’d run into traffic or walk off a dock.

I didn’t know I’d always have to be on high alert.

I didn’t know how much protection he would need. His vulnerability is unbelievable.

I didn’t know people would stare at us.

I didn’t know I’d have to prove his worth repeatedly to a world that often overlooks him.

But there are other parts too.

I didn’t know a hug or a touch could be special.

I didn’t know a sound or a word could mean so much.

I didn’t know how much I could fiercely protect someone.

I didn’t know how I would look at my life, with unbelievable amounts of gratitude, and thank God for what I have been given. Because we are the lucky ones. 

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, subscribe for exclusive videos, and subscribe to our newsletter.

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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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