Tears of Joy: A Yearbook Photo’s Impact

There are quite a few stories in the news right now about kids with disabilities being excluded from events at school. This happens every year. And as mom to a child with nonspeaking autism, reading them hurts. Because I know. I know what it feels like to have a misunderstood child. And feel like you don’t belong. It’s an ache. It’s a deafening silence. It’s hope. It’s anger. Its frustration. It’s more. I’m sharing this with you because something beautiful happened. Something I didn’t expect. And it has humbled me.…

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Summertime on the Spectrum

Summertime is different for some kids… So many of you are asking me about Cooper’s summer plans. A valid question. He finishes up school this week. Then he will be an eight grader. He absolutely understands that school is almost done for the year. I know because yesterday when we walked him to the bus he held up three fingers the entire way and had us repeat…’three more days.’ He likes his reassurance that one. Summer breaks are different for kids like Cooper. Or maybe it’s just him. I guess…

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He Deserves to Live with Dignity and Respect

And then she said, ‘you are so lucky that your son doesn’t care what he looks like. Or care about the latest trends in clothes or even what his hair looks like. It’s so hard these days to keep up.’ She finished it with, ‘I bet he doesn’t even care what you dress him in…’ I’ve been thinking about that conversation for over a week now. I know what she was getting at. I know what she was implying. She was telling me I was lucky that my kid didn’t…

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Looking at Hope in a Realistic Way

Hope. Gosh I hear that word a lot. Have hope. Never give up hope. All we can do is hope. If we give up hope, than what do we have left.’ In the world of special needs, hope is a hot topic. Hope and I have had a rocky relationship over the last few years. For years I hoped nothing was wrong with my baby. Then I hoped my toddler would catch up. And then I hoped that it was ‘just’ a speech delay. Then I hoped it wasn’t autism.…

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We Attended a United Dance Together

The child you have right now is not the child you will have forever. Let that sink in. You can also say the hard that you have now right now is not the hard you will have forever. Years ago, when my son was 4 and 5, and autism was new, we were really struggling. This sweet boy couldn’t communicate. He didn’t feel well. He had anxiety and adhd that seemed to consume him. We couldn’t leave the house. We didn’t sleep. We didn’t stop moving. We quite literally never…

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Am I Brave Enough…?

I just left the grocery store. I only had a few things today so opted for the self checkout today. While I scanned my items, I became aware of two young men next to me. I would say they were both in their 20’s. It dawned on me rather quickly that one was helping the other shop for groceries. He was helping him scan each item, slow and meticulously. Talking him through he step. The gentleman being helped was very much enjoying himself. He was laughing and making very happy…

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Mother’s Day and Inclusion

There is a memory I often share about Mother’s Day. In fact I think it’s even in my book. It impacted me so deeply. So much so that I’m still talking about it 11 years later. My son Cooper is the one who first made me a mom. Today he is 13 years old. He has a diagnosis of severe nonverbal autism. I like to tell the moms and dads of newly diagnosed children that it takes time. Every part. Acceptance. Understanding. Advocacy. It all takes time. Eleven years ago,…

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A Mother’s Letter to Her Autistic Teenager

Kate and Cooper

My son, I like to write you these little notes so that one day, when I’m old and gray, and my memory isn’t so good, I can remember you. Your life. And us. You are 13. You are a teenager. When you were diagnosed with autism all those years ago, and the future felt confusing, maybe even a little bit scary, I would wonder what you would be like at this age. Because the teenage years can be interesting. And autism, well it muddles the edges. There are no ‘what…

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‘What Kind of Autism Does He Have?’

I get that question a lot lately. It typically comes from someone new to my life. A fellow sports parent. A stranger at a party. A grandparent at the park. See when I tell people I have four kids, ages 2 to 13, people ask questions. What schools do they go too? What sports do they play? Do you know so and so? My son is 13 too! I tell them about each of my kids, with pride and love and humor. I share stories like all moms. The stories…

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Don’t Forget About the Siblings

Really sweet story I wanted to share with you. My son Sawyer is 11 years old. When I describe him I use words like smart, athletic, kind, and empathetic. I honestly think he got the best parts of his Dad and me. And of all four of my kids, I worry the most about him. That surprises people sometimes when I share that. But he’s my tender one. He carries the most. And he worries the most about his brother Cooper who is autistic. The other day, during a game,…

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