Our Stories Are Not All the Same

This will be my most unliked post, and I get it. I’m never trying to “start something” or offend anyone, but I do want to be honest in how I feel on this journey.  My name is Danielle. I share our families journey at Story of Noahism. I made a tiktok a couple weeks ago and on that app comments get a lot of attention. More so than IG. And one of my top comments meaning hundreds, almost 1k to be exact, of ppl have liked it, goes something like…

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The Ebbs and Flows of Autism

Early this morning our daughter came into our room, hopped into bed next to me, and began working on her intricate mindfulness sticker book. I watched as she elaborately and precisely filled out each piece of the picture, quicker than I ever could. A beautiful sight.  I said “good morning, sweetie”, but did not get a noticeable response. Craving interaction, I asked her what she was making a picture of in her book. Sadly, again there was no response. So, I re-asked, even more enthusiastically— still no response. Then I…

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I Never Stopped Talking To Him

Yesterday I interviewed my dear friend Leasa of Cody Speaks. If you don’t follow her you should. Her son Cody is 20. He loves videos and the mail. His autism was discovered when he was 17 months old. And he started talking at 9 years old. When she said that on the live, comments immediately came in asking what she did. What is the magic thing that got him to start talking? I understand because when I found Leasa and Cody, I asked the same question. My son was 7…

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Never Ever Give Up Hope

Our family’s number one goal is to get in the community together. It’s never really happened. Well, not successfully. But we refuse to give up. Tonight, our middle son had flag football practice. I wanted to go. My husband wanted to go. We wanted to get the other two boys out of the house. So, we did it. Cooper’s motivator and encouragement…two (not one!) vintage train magazines from eBay. His most favorite thing in the world. We stayed an hour. I have never, in nine years, been more proud of…

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Being Invisible

There are many beautiful things that I was gifted when I entered the world of special needs. Things that most people outside of our world know nothing about. Because they are unique to us. To our world. There are honestly to many to list. But one that rises to the top is that I get to see the people who see Cooper. One would think that a 9-year-old boy who dances in the rain and wears brightly colored leggings couldn’t possibly be overlooked. But it happens every day. People hear…

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Doctors And Nurses: Thank You

This little peanut had an outpatient surgery this morning. Nothing too serious. But nevertheless it needed to be done. I want to say the hugest thank you to Pediatric Surgical Associates, LTD and Children’s Minnesota for providing outstanding care. Harbor was charming, patient, darling and easy. It went as smooth as it possibly could have. And everyone was so kind to us. For anyone who has followed us for a while, you know that my older son Cooper is no stranger to different procedures. This mama has spent many hours wandering the halls of…

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Your Ups And Downs

Some days I wish I could just press reset. Or snap my fingers and make life easier for you. But I can’t. It doesn’t work that way. Instead it feels like ups and downs. Today you had an amazing speech session. The best in months! I think we gave you a hundred high fives. But then when it was over you dropped to the ground in the lobby and refused to get up. It was hard. It was over paper. You also kept a bandaid on your toes. You are…

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The Future Of Autism

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…

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Well-Child Visit

This little guy and I just came from his 18-month well-child visit. He’s 22 months actually so I was late. But only by four months. Not too bad if you ask me. I blame Covid. But really it’s because life is crazy and he’s healthy and we are all thankful to be able to avoid the doctor’s office right now. I have two other boys too. Cooper is 9. Sawyer is 7. I don’t remember any of Sawyer’s baby visits. I think because they were easy. He was easy. He…

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The Things I Wonder

Kid, I spend a lot of time thinking about the things you cannot tell me. There are little things. Like why you point to certain clouds or put your ear up to the wind and laugh. There are big things too. Like why you hit your head in frustration. Does it hurt? Do you hear something I cannot? I wonder why you like trains so much. I wonder why you carry the DVD cases but don’t watch the movies. I wonder if you are lonely. I wonder if you get…

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