Our 2017 Year in Review

I often find myself talking about all the things my autistic son can’t do. I don’t mean too. I’m not negative. I’m just human. And when you get together with a friend who also has an autistic child you start listing out where they are at. Yes, they are nonverbal. No, this and yes, this. And before you know it the things they can’t do outweigh the things they can do. I worry about where he is at. I get overwhelmed by how far he has to go. Sometimes I…

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January Guest Blogging Writing Challenge

Hi all! Thank you to everyone that submitted an ‘I am Thankful’ post in November and December. As we turn to the 2018 I’d like to change up the blogging topic! Every year on Sawyer’s birthday I write him a letter. I started when he was two. You can see last year’s letter below. Over the years I’ve started writing letters to the people that have played a role in our autism journey. Friends, family, strangers, even Cooper. Some times I thank them. Some times I apologize. And every time…

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I Changed My Way of Thinking and it Changed My Life

As a mom to a little boy with autism I live by the quote: ‘I changed my way of thinking and it changed my life.’ I haven’t done a video in over a week! In this (long) video I give an update on our life and then discuss my evolution as a mom to a child with a lifelong disability. I get asked daily if I really am as happy and positive as I appear in my videos. The answer is yes. 95% of the time my sons disability motivates…

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9 Big Mistakes Parents of Autistic Children Can Avoid

I often think of my son’s autism as a journey. A journey that not only he is on, but our family as well. A journey with many, many challenges. And holes and cliffs. And of course it’s slippery.  The hills have jagged rocks and most of the time I feel like I am hanging on for dear life. There is no safety harness or map. I typically don’t know if I am even going in the right direction. And perhaps at times I fear that I might be going backwards.…

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Will It Always Be This Hard?

I read a blog post today. It was written by a super exhausted mama for the super exhausted mama. Which obviously caught my eye. That’s me. I work full time. Two kids. One with autism. Three dogs. Home owner. Friend. Daughter. Spouse. I spend my days sharing autism, advocating, attempting to have a social life, trying to drink enough water, playing with my kids, exercising, fighting with Cooper over eating and communication, cooking dinner, cleaning my house, wishing I could walk my dogs, get a good night sleep and pee…

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I’m Thankful For You: The Child Who Defends My Daughter

This December I want to thank and honor the one child that defends my autistic daughter in school. I want you to know that I hear the positive things you are doing. I know you are sticking up for my daughter. And I can never thank you enough. My daughter Lillian was first diagnosed with autism when she was four years old. I had a hard time trusting this diagnosis because there wasn’t much testing done at all. We went the next few years without much help until Lillian was…

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A Conversation with Sawyer: Is My Brother Coming With?

A few nights ago, Jamie and I attended our four-year-olds first Christmas pageant. I can’t even tell you how excited I was to attend. Sawyer had been talking about it for weeks. I knew it was going to be special. Sawyer nailed it. Just like he always does. He stood, sang, participated and hammed it up. And we watched. It was wonderful. It was pretty special to watch him. My little Sawyer’s first Christmas concert. He’s a star! And also appears to have some emotions midway through. He’s on the…

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Does Parenting A Child With Special Needs Get Easier As They Age?

Have you ever wondered that? I used to all the time. I would be at a particularly low point in our Autism journey and I would ask that question to my mom or a friend or a doctor. And no one would tell me the truth. I just needed to hear if it was going to get easier or get harder. I needed an honest answer. The problem was I was asking the wrong people. I’m not surprised I get asked this question every day by parents of newly diagnosed…

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A Conversation with a Stranger

Last week I helped a father while his daughter was in the middle of an autistic meltdown. We’ve all been there. As the parent your focus is safety and getting through the meltdown. This man needed an extra pair of hands. And I had no problem offering mine. After she calmed down we had a quick conversation that has stuck with me. Without knowing each other, or saying much more than an introduction, he said, ‘I didn’t know how hard it was going to be. And I really didn’t know…

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How Does My Autistic Son Fit Into The Real World?

We spent the weekend at a water park. I will be honest when I say I was very worried about it. The trip involved a long drive, a hotel stay, waiting, walking, crowds, chaos, etc. You get it. Bringing Cooper somewhere like a water park would traditionally threw off his schedule for weeks. We’d go, have a really tough time and then come home thinking it would be better once we got him back into his routine with his things. Except we were wrong. Cooper, and our family, felt the…

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