Neurodivergent Conversations | Autism, ADHD, AuDHD, PDA, Emotional Regulation, SEND parent, Meltdowns, Special Needs Parent

If sleep feels like the hardest part of neurodivergent family life, you’re not imagining it—and you’re not failing. In this episode, Greer Jones talks with sleep specialist Melisa Moore about why neurodivergent kids (and adults!) often have more sleep challenges… and what can actually make things gentler.

Melisa breaks down the “why” in a way that’s clear and grounding: biology and genetics can play a role, circadian rhythms can be different (like ADHD tending later and autism sometimes being inconsistent), and some neurodivergent profiles come with a higher likelihood of specific sleep disorders. Then there’s the big real-life layer: things like allergies, eczema, reflux, anxiety, and more—stuff that isn’t “a sleep disorder,” but absolutely messes with sleep.

From there, you’ll get practical support that doesn’t demand perfection. Melisa shares her “5 S’s” of bedtime routines—short, sweet, sensory-soothing, streamlined, and steady—and offers permission to stop chasing the ideal. Even a bedtime routine once a week can help.

You’ll also hear a refreshingly nuanced take on screens: the research isn’t as black-and-white as “all devices ruin sleep.” For some kids (and adults), a little screen time can quiet the brain enough to fall asleep faster—and you can still move toward “good, better, best” without turning bedtime into a battle.

Finally, if your child wakes in the night and needs the exact same sound/light setup to settle again, you’ll understand why—and what to tweak so everyone gets more rest.

In this episode, we talk about:

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If your life feels like a beautiful, noisy jumble—kids, work, relationships, responsibilities, and about 47 open tabs in your brain—this episode will feel like a deep exhale.

Greer Jones sits down with Jessica Lamb (mom, business owner, podcaster, and recently diagnosed ADHDer) to talk about what it’s actually like to hold all the roles at once—especially when you don’t naturally compartmentalise and everything feels layered on top of everything else. Jessica describes family life as “chaos,” but not in a hopeless way—more like: this is the water we swim in, and we’ve learned how to live here.

They get honest about the season of early motherhood and how ADHD can show up hard when executive functioning takes a hit—right when you’re trying to learn how to be a parent. Jessica shares that she’s still figuring out what “self-care” even means for her, but one thing is clear: therapy is her anchor—a predictable space to decompress and untangle the mental knots.

You’ll also hear the kind of practical, real-life support that doesn’t require a perfect routine:

Jessica also talks about redefining success as an ADHD entrepreneur—success as the right systems, the right number of clients, and work that supports the life you actually want (not just what looks impressive from the outside). And in a moment that will make so many ADHD brains feel seen, she shares how she’s learned to stop shaming her procrastination and instead build around it—setting herself up so deadline-time focus becomes a strength, not a moral failure.

This episode is for the mom who looks “put together” on the outside but feels like a duck paddling furiously underneath. It’s a reminder that you’re not behind—you’re adapting. And a little more grace (from you and from others) goes a long way.

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Have you ever noticed that fun is usually the first thing to go when life gets hard? When the budget is tight, when you're exhausted, when you're running on fumes — fun feels like a luxury you can't afford.

But what if that's exactly backwards?

In this episode, Greer sits down with Annie F. Downs — author, podcaster, and all-around fun enthusiast — for a conversation that feels like a warm exhale. Annie gently challenges the idea that fun has to be big, expensive, or perfectly timed. She makes the case that the moments we need fun the most are usually the ones where we think we can't have it.

Together, Greer and Annie explore:

This episode is for any mom who has quietly stopped doing the things that used to light her up — and who needs a gentle reminder that she still matters in the equation too.

You don't need a vacation. You don't need three days off. You might just need a slushie, a craft store, and permission to play again.

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Don't forget to grab your FREE ticket to the Everyday Neurodivergent Parenting Summit happening May 11-14!

If you've ever felt like motherhood was supposed to be the thing that finally felt easy — and instead it somehow got harder — this episode is for you.

Greer sits down with Amy Marie Hann, ADHD coach and mom of neurodivergent kids, for an honest, grounding conversation about what it actually feels like to parent with ADHD. Not the productivity-hack version. The real version — the shame, the overcommitment, the mental load that never seems to let up.

Amy talks about why ADHD moms are so prone to over-extending themselves (hint: it's not a discipline problem — it's how your brain processes time and priority), and why the gap between the mom you imagined being and the mom you are right now can feel so painful.

But this isn't a heavy episode. It's a hopeful one.

Amy shares where to actually start when everything feels urgent and overwhelming — and it's not another complicated system. It's something much smaller, and much more doable. She also talks about why taking care of yourself isn't selfish — it's one of the most powerful things you can do for your neurodivergent kids.

They also get into something that feels quietly important: safety. What it means to find environments where your family can actually exhale. And why, as the mom, you often have to be the one who goes first.

In this episode, you'll hear about:

You are the right parent for your child. Even on the hard days. Especially on the hard days.

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If you've been waking up exhausted before the day even starts, moving through the hours in a fog, snapping more than you want to, and quietly wondering what happened to the version of you that felt okay — this episode is for you.

Greer sits down with Irin Rubin, founder of MamaZen, for one of those conversations that feels less like an interview and more like someone finally saying out loud the thing you've been carrying alone.

Irin spent years in maternal burnout before she found something that actually helped — and it wasn't a planner, a routine, or another self-care tip. It was learning to regulate her own nervous system first. And everything changed from there.

In this conversation, Greer and Irin talk about:

This episode is especially for moms raising neurodivergent kids — many of whom are navigating their own nervous systems at the same time. There's no judgment here. Just honesty, warmth, and a quiet reminder that you are the anchor. And anchors need tending too.

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If you've ever felt like you're living on the edge of yourself — keeping everyone else afloat while quietly disappearing — this episode was made for you.

Greer sits down with Michelle Anderson, founder of JMB Inspired and host of the Radiant Moments Caregiver Oasis podcast, for an honest, deeply human conversation about what it really means to be a caregiver inside neurodivergent and medically complex family life.

Together, they explore the parts of caregiving that don't get talked about enough: the always-on mental load, the invisible emotional work, the loneliness of asking for help and not knowing how, and what it feels like to one day realize you can't remember what you even like anymore.

But this episode isn't just about naming the hard stuff. It's about finding your way back — in micro moments, in community, in tiny choices that say I matter too.

In this episode, you'll hear about:

The mental and emotional load that never really switches off — and why "just relax" isn't the answer. How micro moments and habit stacking can quietly rebuild your regulation without adding to your plate. Why "call me if you need anything" often leaves caregivers more isolated — and how to ask for and offer specific, real-life support. What it feels like to lose yourself inside a caregiving role, and the gentle, small ways you can begin to find your way back. The kind of community that actually helps — and why it's okay if it looks completely different than you expected.

This conversation is warm, practical, and full of the kind of honesty that makes you exhale and think yes, that's exactly it.

Whether you're a neurodivergent mom, a parent of a neurodivergent or medically complex child, or simply someone who has been carrying too much for too long — you are not alone, and you're allowed to be part of your own care plan.

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If you’ve ever thought, “Why can’t I stay calm when my child is melting down?”—this episode wraps you in so much compassion, without letting you off the hook in a shame-y way.

Greer Jones is joined by Lisa Candera, an autism mom of 18 years who built the kind of support she couldn’t find anywhere: support that starts with the parent’s regulation first—because (as Lisa says) we are our children’s environment, and emotions are contagious.

Together, they talk about the real reason “just be consistent” isn’t enough when you’re parenting a neurodivergent child: you’re often living in a hyper-vigilant state, your nervous system is already on high alert, and the moment things go sideways, your brain goes straight into default mode.

Lisa shares a powerful starting point that’s simple-but-not-easy: do less. Pause. Stop jumping in to fix it. Create space between what’s happening and your response so you can respond with intention instead of reacting from fear (fear of judgment, fear about the future, fear you’re “doing it wrong”).

They also reframe meltdowns in a way that’s honestly a relief: the meltdown isn’t proof you failed—it’s information. A sign that something was a “bridge too far” that day. And from there, you can get curious instead of personal.

You’ll walk away with grounded, in-the-moment tools (like deep breathing and tapping/EFT) and a deeper reminder: neurodivergent is not just a label—it’s a whole different operating system. Respecting that changes everything.

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What if the first positive thing connected to your child’s diagnosis was… a dog in a little jacket that makes people smile?

In this episode, Greer talks with Robbie Campbell from Buddy Dogs, a service within Guide Dogs UK that places specially matched dogs with children who have vision impairments—often alongside other complex needs. Robbie explains why Buddy Dogs exists: guide dogs are trained for mobility and require a level of independence that simply isn’t realistic for most children. But the companionship, confidence, and connection that dogs bring? That can be life-changing for kids and families.

Robbie shares what he sees again and again: dogs becoming an “icebreaker” in public, helping kids feel more confident talking to others, and even opening doors for children to speak about their vision impairment in a new way—sometimes for the very first time. For some families, the Buddy Dog becomes a shift in the emotional story: instead of isolation and heavy equipment drawing stares, there’s a warm, inviting focus that brings people closer.

You’ll also hear how Buddy Dogs are different from guide dogs: Buddy Dogs aren’t trained for mobility tasks. They’re placed for companionship and day-to-day confidence-building—and they’re typically dogs who didn’t continue down the guide dog route, but are still beautifully suited for family life. Matching is taken seriously, including what a particular dog needs and what each family’s lifestyle can support, with training and ongoing check-ins to make sure the partnership stays strong.

The conversation also touches on neurodivergent families: many kids in the programme are also autistic, ADHD, or otherwise neurodivergent. Robbie describes how dogs often become natural regulators—helping with transitions, reducing anxiety, and bringing grounding presence (without being “task trained” like some assistance dogs). One story stands out: a child who arrived at a session as a whirlwind of anxiety and energy, then settled and connected once the dog entered the room—and after being matched, showed a remarkable shift in focus, communication, and calm.

Greer also shares her own experience: how giving her son simple dog-care “jobs” after school (feeding, playing, petting) has helped soften the tricky transition from school to home—because sometimes that repetitive, comforting connection is exactly what a nervous system needs.

This episode is a reminder that so much of disability and neurodivergence is invisible—and we never fully know what someone is carrying. Robbie’s takeaway is simple and powerful: be open, be curious, and be willing to support people as they are.

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Some kids don’t fall apart at school or out in public. They hold it together all day… and then unravel the second they walk through the front door—because home is the safest place their nervous system knows.

In this episode, Dr. Arielle Schwartz (psychologist, author, and mom) shares the story of how she “followed the clues” to understand what was really going on for her son—starting long before the word dyslexia ever entered the picture. She takes us back to early signs like sensory processing challenges, a highly sensitive nervous system, and delayed language development—plus the frustration of having a bright mind with big feelings and not enough ways to get it all out.

As school demands increased, the gaps became more visible—especially around reading. Arielle describes the heartbreaking moment when her son didn’t just avoid books… he hid from them—and how the shame of feeling “different” can show up shockingly early. One turning point came from an unexpected place: a film about dyslexia that helped her finally name what she was seeing and pursue a full evaluation.

From there, she opens up about what the diagnosis clarified (and what it didn’t), how hard it can be to find the right interventionist (not just the most qualified on paper), and why felt safety is everything for kids who freeze, shut down, or hide when learning feels threatening. She also shares how advocacy with schools can be both exhausting and necessary—and how one committed teacher chose to learn, grow, and become part of the solution.

And then comes the hope-filled part: the “game changers” that helped her son begin to see himself differently—community, mentorship, movement, and being surrounded by people who reflected back what was possible. You’ll hear why programs like Project Eye to Eye mattered so much, why some kids need parents out of the homework battle to protect the relationship, and how a few key supports can slowly unwind years of shame.

This conversation is tender, honest, and deeply reassuring—especially if you’re in that phase of parenting where you’re thinking, Is it my instinct… or am I overreacting? Arielle’s story is a reminder: your noticing matters. And with the right support, your child’s future can look so much brighter than it feels right now.

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If you’re parenting a child with ADHD (or you’re late-diagnosed yourself), it can feel like you’re constantly trying to “figure it out” — schedules, school, food, sleep, behaviour, emotions… all of it.

In this episode, Greer talks with Dr. Jennifer Dall about approaching ADHD through a whole-person lens: not as a “fix,” but as support for real life. They unpack why the basics (sleep, movement, food, connection) matter so much — and how to build strategies with your child so it doesn’t all sit on your shoulders.

What we cover

A gentle takeaway

You’re not failing. This is a learning process — for you and your child — and small shifts can make a big difference.

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