Feet Bigger Than Mine: A Mother’s Journey with Autism

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I don’t talk about our challenges associated with autism all that much any more. Some followers assume that life is easier now. Or our son is less autistic.

Neither of those things are true. Cooper is still very much significantly affected. But he is also wonderfully supported.
We, his family, our friends, his team, we know how to support him. And because of that…he is thriving. We all settled in as I like to say.

I’m not afraid to share either. It’s not that. I have my reasons. Ones that involve stigmas and dignity and well…I want to give hope to parents of newly diagnosed kids.

I want them to see my son’s beautiful progress when they Google severe nonverbal autism at 1 am.

I have moments sometimes though. Ones that cause me to pause. To take deep breaths. To feel all the feelings associated with this life we live.

This morning I was helping my son with his socks. At 12, he can put his socks on all by himself. A huge victory. One that we worked on for years. But often the socks are bunched and upside down. So I like to assist him. To make sure they are comfy.

I was checking his feet. As I do daily. His toes. Looking for any sign of self injuring. Checking the bottoms and tops and toes for owies that he can’t tell me about.

When I realized something.

The feet I was holding were bigger than mine.

Not tiny. Not even little.

And the fear. The worry. The wondering. The emotion. It all flooded me. And I fell out of my crouched position onto the floor at his feet.

And just paused as I looked up at him.

He was dancing in the chair to a Chuggington song. His hands were happy. His smile huge.

He is 13 years old. He is no longer a little boy. And many of his cares are still like a toddlers.

Today, I want to say out loud, and feel all the feelings. Because they are real. Because he is so loved. Because I’m scared sometimes. Because he’s growing older. And so am I. And I don’t know all the answers or what the future holds.

I’m terrified sometimes. And no one talks about this stuff. The constant battle to hold back the fear and pretend to put on a brave face and be invincible.

This secret world of autism.

Green checkered Vans. The shoes we share now. Mom and son.

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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