Beautifully Complex

Worry can feel like love. When you're raising neurodivergent kids, worry can even feel like the responsible thing to do. But worry quietly pulls our attention inward, and our kids' nervous systems notice. In this episode, I'm joined by psychologists Dr. Susan Bauerfeld and Chris Parrott, co-authors of “Base Camp Parenting: Worry Less to Help Your Kids More.” They offer a framework I love. Our kids are out there climbing their own mountains, and our role is to be the base camp, the place they return to rest, recover, and make sense of what happened on the climb. A base camp leader doesn't climb for their child or drag them to the summit. They help them take the next step. We talk about the real difference between concern and worry, and why concern keeps us focused outward on what our child needs, while worry turns us inward to manage our own discomfort. Chris and Susan walk through their process for catching worry in the moment: spotting it, noticing and naming what you feel, normalizing it, asking whether the alarm is actually helping, and exhaling to reset your nervous system. We also explore how kids look to us to answer the question "Are we okay?", why a parent stuck in alarm can keep a child stuck there too, and the simple shift from worry to wonder that opens up possibilities instead of shutting them down. If worry has become the background noise of your parenting, this conversation offers a gentler, more grounded way forward, for you and for your child. Listen to the full episode now.

Take the free quiz to find out where to start with your neurodivergent child: parentingadhdandautism.com/quiz

Show notes and more resources at parentingadhdandautism.com/381

Become a supporter of this podcast: https://www.spreaker.com/podcast/beautifully-complex--6137613/support.

You can find additional resources at parentingadhdandautism.com. It's not just about the struggles, it’s about progress, one step at a time.

Some mornings, the most dysregulated person in the room isn't your child. It's you. And that doesn't make you a bad parent. It makes you human, with a nervous system that's been hypervigilant for a long time.

In this episode on nervous system regulation for parents of neurodivergent kids, I'm getting honest about my own history as a yeller. When my son was little, I raised my voice to break through his non-stop energy and get us out the door. What I didn't know then was that I was co-escalating with him, two dysregulated nervous systems pulling each other further into the fire.

We talk about why co-escalation is the flip side of co-regulation, and why it drains your battery so fast. I share how to apply the same behavior-as-communication lens you use for your child to yourself, so yelling or shutting down becomes a signal of what you need, not proof of a character flaw. You'll hear the body cues and triggers to watch for, a simple breath you can use in the hardest moments, and the words I use to explain the science of a dysregulated "bodyguard" to kids so you can both take a break.

We also dig into repair, why it matters more than perfection, and what it can sound like after you've said things you wish you hadn't. And we get proactive, with small daily glimmers that help fill your own battery in as little as three to five minutes a day.

If you've ever lost it with your child and then spent the rest of the day in shame, this episode is for you. You matter too.

Listen to the full episode now.

Take the free quiz to find out where to start with your neurodivergent child: parentingadhdandautism.com/quiz

Show notes and more resources at parentingadhdandautism.com/380

Become a supporter of this podcast: https://www.spreaker.com/podcast/beautifully-complex--6137613/support.

You can find additional resources at parentingadhdandautism.com. It's not just about the struggles, it’s about progress, one step at a time.

Kids notice far more than we give them credit for. They already know reading takes longer, focus slips away, or conversations feel harder for them than for their friends. Without an explanation, so many neurodivergent kids land on the most painful story available: I'm the problem.

In this episode, I'm joined by pediatric neuropsychologists Dr. Katia Fredriksen and Dr. Yael Rothman, authors of the “Different Thinkers” book series, to talk about one of the questions I hear often from parents: how do I talk with my child about their diagnosis?

We get into why so many of us fear a label, and why giving our kids words for how their brain works often brings relief, community, and the beginnings of self-advocacy. Yael shares how she starts the conversation long before an evaluation is finished, by getting curious and using a child's own words to describe what's hard. Katia explains why it helps to sort through our own feelings first, how to choose a calm, connected moment, and how a teacher conference or a recent appointment can open the door naturally.

We also get practical about the moment many parents dread, when a child asks, "Does this mean I'm broken?" You'll hear how to name what's genuinely hard without sugarcoating it, while weaving in real strengths, support, and hope. I share the simple activity that changed everything for my own son, and pulled me out of fix-it mode for good.

When kids understand their brains, shame loosens its grip, and emotional regulation gets a little more possible. This isn't one big talk. It's an ongoing conversation that grows as your child grows.

Listen to the full episode now.

Take the free quiz to find out where to start with your neurodivergent child: parentingadhdandautism.com/quiz

Show notes and more resources at parentingadhdandautism.com/379

Become a supporter of this podcast: https://www.spreaker.com/podcast/beautifully-complex--6137613/support.

You can find additional resources at parentingadhdandautism.com. It's not just about the struggles, it’s about progress, one step at a time.

I put a lot of my own body image struggle onto my daughter without ever meaning to, and I didn't catch it happening until it already had. That's exactly the kind of quiet, unintentional pattern Erin Washington and I dig into in this conversation.

Erin spent two decades cycling through anorexia and exercise bulimia, much of it hidden behind being the perfectionist, the straight-A student, the driven athlete nobody worried about. She's now the author of several books, including her newest, I'm Just Like Me, and the founder of the Blue Butterfly Foundation, which pairs teen girls struggling with self-image and body image with mentors who've lived through the exact same thing.

We talk honestly about what it actually looks like to model a healthy relationship with food and your own body in front of your kids, why physical compliments can quietly teach a child that beauty is their most important trait, and how something as small as a comment in the mirror or a diet before a big event gets absorbed by a watching child far more than anything you say directly to them. Erin also shares how representation shaped her own daughter's sense of what's possible, and why she wrote a children's book explaining, in simple terms, why none of us are supposed to look like anyone else.

If you've ever wondered whether you're passing along your own body image noise to your kids, or you're just looking for language that helps your daughter feel more at home in her own skin, this conversation is full of real, doable shifts you can start using today.

Listen to the full episode now.

You can find additional resources at parentingadhdandautism.com and Regulated Kids.com — because it's not just about the struggles, it's about progress, one step at a time.

Show notes and more resources at parentingadhdandautism.com/378

Become a supporter of this podcast: https://www.spreaker.com/podcast/beautifully-complex--6137613/support.

You can find additional resources at parentingadhdandautism.com. It's not just about the struggles, it’s about progress, one step at a time.

My own kid has told me for years that talking to people online is just easier than talking to them in person. I used to wonder if that was a red flag. Andrew Fishman helped me understand that it actually might be the opposite.

Andrew is a licensed clinical social worker and author of “Parenting a Gamer” who specializes in the impact of video games on mental health. He spent years running group therapy for autistic kids, teens, and adults before focusing his practice on adolescent gamers, many of them neurodivergent.

In this episode, we get into why gaming can feel like the safest, most predictable place in a kid's whole day, especially for a kid whose brain works differently than the world around them expects. Andrew breaks down why success in a game is actually guaranteed in a way it almost never is in real life, why that fairness matters so much to a kid who's used to things not going their way, and how the social rules inside a game, like no eye contact required, no reading of body language, can strip away exhausting layers of decoding for an autistic or ADHD kid.

We also talk honestly about safety, the parental controls that actually work, what to do when your kid gets pulled into online conflict because their sense of justice won't let something slide, and why the meltdown at transition time usually isn't really about the game at all. Andrew shares the question that changes everything when your kid won't log off, and a handful of specific games worth knowing about, including one built specifically to help autistic kids practice social skills.

If gaming has ever felt like a battlefield in your house, this conversation will change how you see it. Listen to the full episode now.

You can find additional resources at parentingadhdandautism.com and Regulated Kids.com — because it's not just about the struggles, it's about progress, one step at a time.

Show notes and more resources at parentingadhdandautism.com/377

Become a supporter of this podcast: https://www.spreaker.com/podcast/beautifully-complex--6137613/support.

You can find additional resources at parentingadhdandautism.com. It's not just about the struggles, it’s about progress, one step at a time.