Posts that talk about our general life as a family fall into this category.
Sawyer often tells me he feels like a failure, or that he feels like he’s stupid. He has told me multiple times now that he doesn’t know why he’s even alive. I tell him “God doesn’t make mistakes, and He made you because He thought the world needed one of you.” What I don’t tell Sawyer is that I feel like a failure because I can’t just magically make him feel better.
To all those parents out there struggling to keep going and keep being everyone’s cheerleader while you, yourself, are struggling- I see you.
A single day or month for world autism awareness never feels like enough and sometimes feels a little laughable because every day in our house is autism awareness day. There isn’t a day that goes by that our lives are not affected by autism and its nuances.
Do you ever look at or think about your kids and just feel overwhelmed with love and pride? I’ve had a lot of those days lately…
The most important news first: Sawyer is doing better.
In 2025, nobody should be using the r word anymore; it’s NOT ok.
Last night Sawyer asked me a question I’ve been waiting for since we first told him about his autism diagnosis: ” Momma, why do some kids in a family have autism and some don’t?”
I have been asked several times since starting this blog if I am worried that I’m sharing too much about Sawyer, or our life as a family. And honestly, sometimes I do worry about that. But the goal of this blog has and will always be to share our experiences as an autism family as a means of encouraging autism awareness and understanding.
Like a lot of people, I love spreading the word when I find something that I think is awesome. Whether it’s a great recipe, a new makeup item I can’t live without, a super cute shirt that’s flattering and affordable, or a product that makes life easier for me and my family.
Sawyer may be outgrowing my lap, but in my heart he will always be my baby boy.
A lot has happened since the last time I wrote.
After giving it a lot of thought, I’ve decided to move to Tennessee. Not only will it allow me to be at more of Caitlyn’s events and competitions, it will bring my children back together and give Sawyer more time to spend with his dad.
Our goal is to help share support and resources with families like ours. ♥
We love sharing when we find awesome places and things! Click the heart to check out a bunch of stuff our family loves!
Vanderbilt Kennedy Center is a very special place to our family. It’s where Sawyer was first diagnosed with autism, and it was through their incredible programs and research that he first received the therapy he needed to thrive. Our current political administration has pulled funding that pays for progams and services that help families like ours. Please consider donating to VKC to help others continue to receive the vital programs and services needed to help them succeed.
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