The Comment Said “It’s always about the special needs kids…”

The comment said…It’s always about the special needs kids. You parents are always whining for them to get everything.” That comment was from a while back and it was in response to a post about how children with special needs/disabilities were forgotten during covid. A bold statement yes, but also true. It was made be a lady. One the same age as me. One with kids. She felt that everything is just handed to kids in special education. The statement has been in my head for a week now. Running…

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We Have IEP Wounds

I read a post this morning from the amazing Jillian Benfield about IEP Wounds. I believe everyone should read it. And I believe that words come into our lives at the exact moments we need to read them and feel them. I felt the tears start to fall this morning while I simultaneously nodded along with her words. I’m not going to rewrite what she wrote because she said it perfectly. But here is what I want to tell you. After yesterday, I, me, my husband, our son, we have…

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Little Big Things

When I share my son’s autism, my favorite parts to share are the little big things. The moments that happen that are so huge, yet so subtle, that sometimes I don’t realize they happened until hours later. Like this morning. At 3 am. When I was awake with a toddler who refuses to develop a love for sleep like her mama. My son Cooper is 11 years old. A tween. A soon to be sixth grader. He loves bullet trains, his grandparents, and episodes of Family Feud. He wants to…

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His Brother’s Safe Space

A few days ago we took a boat ride. Sawyer brought two friends. A brother and sister who are very much a part of our family. The big kids, Cooper included, all wanted to sit in front and screamed at Jamie to go faster. They were also supposed to watch for logs but that part didn’t happen. As we boated along we hit some rough water. It only lasted a minute or so. Pretty common on a Friday on the St. Croix River. Anyhow, Cooper squealed as a bit of…

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Understanding and Acceptance

People get really nervous around individuals who are non speaking. Or folks who use a wheelchair. Or who look different. I didn’t know that before I had my son Cooper. Before he led me wide eyed into the world of disability. Without knowing he showed me how a person can be invisible. A person standing front and center. Some of it’s subtle. The overlooking of a person. Some is not. And it’s hard to see. As his mom it’s hard to not get mad and sad and frustrated. Because I…

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Small Big Things

Something huge happened yesterday. But amidst the chaos of putting on sunscreen and watching kids jump into the pool and picking up wet towels I missed it. I was busy throwing a party. I wasn’t paying attention to small big things. My son Cooper is 11 years old. He loves balloons and parties and the frosting on cupcakes. He said his first word at age 9. It was mom. He says it long and drawn out, pausing on each letter as if he’s plucking them down from the sky. MMM-AW-MMM.…

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A Brave Day

Let me tell you about a boy. A boy who at eleven years old shows more bravery than most adults I know. But his bravery looks different so most overlook it. He has very few words. Not much for conversation. But his eyes…they tell a story. If you listen to him. Patiently. If you don’t rush him. And wait. He will tell you. If you don’t talk over him. Or speak for him. He will tell you how he hears things louder than you. And smells the faintest smells. And…

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I Wish Time Would Slow Down

This one and I needed some time together. At 9 years old he’s in that in between space where he will hold my hand but can run to the concession and grab his own soda. He needs me but doesn’t fully. He lays his head on me when he’s tired and uses his own hand to cover my eyes during the scary parts. He’s not embarrassed of me. But also thinks I’m super old. He loves his siblings fiercely. But asked today if we could go to the movies just…

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Wild Ones

Some kids are just mischievous. Wild. Busy. Exasperating. Curious. Spirited. All words we choose instead of naughty. They see a puddle and have to jump in it. A glass of water and have to dump it. A counter and have to climb it. They see a toy and immediately want to know how it works. How it’s wired. Taking it apart becomes vital. What’s it made of they think. They see mail and need to know what’s inside. A package becomes a possibility. It could be a Nerf gun or…

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Chloe

Yesterday morning our sweet girl Chloe passed away. She has been with our family as long as we have been one. She’s grown with us as we added four babies, seen 8 houses, and aged 15 years. She’s our Chloe girl. She’s a permanent fixture in our life. For 15 years she’s patiently waited at the door for us to come home. She’s lost her hearing and her sight, so we had to gently wake her up when we would get home. We don’t want to startle her. She went…

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