Before the Diagnosis: The Fight That Changed Our Future
A few months after having my light bulb moment (you can read about that in The Truth About Early Autism Signs: A Mother’s Story of Realization and Hope), I finally started accepting that Nolan may have autism and went about setting up an appointment to get him evaluated through the school district.
Unfortunately, autism evaluations aren’t exactly a walk-in service. The soonest available slot was six months out—which, in mom time, feels like a decade. So if you’re reading this and you’re concerned about your child, please don’t wait. Schedule the evaluation now. Even if your child doesn’t have a disability, isn’t it better to know than to spend every night tossing and turning, wondering if you’re missing something? Clarity is a gift. And trust me—wondering every day is way harder than knowing and moving forward.
And here’s the truth that no one wants to say out loud:
The longer you wait to get your child help, the harder it is for them to heal.
Early treatment for autism isn’t just helpful—it’s critical. The brain is most flexible in the early years, which means the window for meaningful progress is wide open—but it doesn’t stay open forever. Every month matters. Every delay makes it harder for your child to build the skills they need to thrive.
If you’re still in the “maybe” stage, I shared our first lightbulb moment in The Truth About Early Autism Signs—it might help you feel less alone.
Becoming the Wrecking Ball Mom
Before the diagnosis, I became a wrecking ball with a Wi-Fi connection. I was on a mission to research everything I could about how to help Nolan heal. I’ve always believed in natural medicine, and I had this unshakable hope that healing was possible—even when people around me said, “You can’t heal autism.”
Spoiler alert: I didn’t listen. And I’m so glad I didn’t.
Even though I had a toddler, an infant, and was working part-time, I spent every spare moment diving into the stories of parents who had walked this road before me. I read every book I could find, joined Facebook groups, and Googled like it was my job. There were days I wanted to quit. Days I cried in the laundry room. Days I questioned everything. But pushing through that fight was the most important thing I’ve ever done.
If you’re in the thick of it right now, hear me: put in the work now, so you can meet your real child later. I wouldn’t know the version of Nolan I know today if I hadn’t fought through those early years.
If your days feel like a sensory circus, The Sensory Breakthrough That Changed Our Days—After Years of Struggle might give you a little hope. And if your mornings start in meltdown mode, How to Recover When the Day Starts in Meltdown Mode is one of the most honest things I’ve ever written.
Awaken Your Mama Bear
And here’s something else I learned the hard way:
You have to awaken your mama bear.
Before the diagnosis, I was still waiting for someone else to tell me what to do. But once I woke up that bear—that fierce, protective, unstoppable part of me—it changed everything.
No one in this world is going to advocate for your child the way you will. Not the doctors. Not the teachers. Not the well-meaning relatives who say “he’ll grow out of it.” You. It’s you.
Once you awaken that bear, you stop waiting for permission. You stop second-guessing. You start gathering the strength you need to help your child, because suddenly, it’s not about fear. It’s about love.
And love is powerful. Love is what fuels the research at 2 a.m. Love is what makes you switch out your cleaning products, overhaul your pantry, and stand up to professionals who don’t see your child clearly. Love is what makes you brave.
Two tools that helped me advocate and teach with confidence were:
Training Aliens – a social skills program that actually gets neurodivergent kids. It’s playful, emotionally safe, and gave me language to support Nolan’s interactions without shame or overwhelm. It helped me see his behavior through a lens of connection, not correction.
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Signing Time– a gentle, joyful way to help Nolan communicate when words were hard. It gave him power, and it gave me peace. If your child struggles with speech, transitions, or emotional regulation, this program is a game-changer. It’s not just about signs—it’s about giving your child a voice.
If you’re still waiting for someone to tell you it’s okay to fight—this is me, telling you:
Wake up the bear. Your child needs you. And you are already enough.
Cleaning the Fish Tank: Where Healing Begins
Before the diagnosis, I didn’t know where to start. But nearly every healing story I read began with one thing: clean up the environment.
I like to think of it as a dirty fish tank.
Imagine your child as a beautiful, sensitive little fish trying to survive in a tank so murky you can barely see through it. The water is filled with chemicals, noise, clutter, and stress. And that grime? It’s not just inconvenient—it’s suffocating.
Your job isn’t to fix the fish. Your job is to clean the tank.
So that’s what I did. I swapped out household products, filtered the air, simplified our routines, and started paying attention to every little thing that could be making Nolan’s world harder to navigate. It wasn’t glamorous. It wasn’t instant. But it was the beginning of something real.
If you’re wondering what that looked like in practice, I’ve shared the exact steps I took to clean up Nolan’s “fish tank” in this post. It’s full of gentle, sensory-friendly swaps and healing tools that helped us breathe again.
If you’ve ever wondered whether that toy your child clings to is “just a distraction,” That Toy Isn’t a Distraction. It’s a Sensory Survival Tool might shift your perspective. And if you’re trying to plan a vacation without losing your mind, How We Finally Enjoyed Vacation with Food Allergies—No Stress, Just Magic is full of practical magic.
What Comes Next
Those six months before the diagnosis were some of the hardest—and most transformative—months of my life. I didn’t have a label yet, but I had purpose. I was cleaning his tank, one choice at a time. And even though I didn’t know what the evaluation would say, I knew I was already showing up for him in the most important way.
In my next post, I’ll share what happened on the day of Nolan’s evaluation—what they said, how I felt, and why it didn’t break me. Spoiler: it actually gave me more hope than I expected.
If you’re homeschooling a neurodivergent child and wondering how to make it work, Neurodivergent Homeschooling Made Simple is a great place to start. And if you’re just plain burned out, Feeling Burned Out? A Survival Guide for Overstimulated Moms might be the hug you didn’t know you needed.
Ready to Take the Next Step?
If you’re walking a similar path, here’s what you can do right now:
- Bookmark this post so you can come back when you need strength
- Share it with a friend who’s wondering if their child might need help
- Subscribe or follow along so you don’t miss the next part of Nolan’s story
- Explore the related posts below for practical tips, emotional support, and real-life encouragement
You’re not alone. And the fact that you’re here—reading, wondering, showing up—is already proof that you’re the advocate your child needs.
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