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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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What if some “addictive behavior” is actually a nervous system trying to cope in the only way it knows how?
In this episode, Greer sits down with Ben Branson (The Hidden 20%) to talk about the overlap between neurodivergence and addiction, especially for people who were diagnosed late and spent years chasing dopamine, trying to regulate, and not knowing why life felt so hard.
They also talk about the bigger picture: long NHS waitlists, siloed assessments, and the painfully common experience of finally getting a diagnosis… and then being handed a letter with zero meaningful support attached.
This conversation is honest, sometimes fiery, and deeply human. It’s about what needs to change, but it’s also about something quieter: how understanding your brain can bring relief, context, and self-compassion.
In this episode, we talk about
Gentle reminder: if this topic touches something tender for you, take it slow. You’re allowed to pause and come back.
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If you’re a neurodivergent parent or you’re parenting a neurodivergent child, burnout can creep in quietly… until it suddenly doesn’t feel quiet at all.
In this episode, Greer talks with Liz (The Untypical OT) about what burnout actually is, why it’s so common in neurodivergent families, and why it’s often not your child causing it. They name the real load: the constant planning, the constant navigating, the constant advocating, and the systems that make everything harder than it needs to be.
They also talk about something that matters a lot: burnout isn’t something you can “self-care” your way out of. It’s nuanced. It’s personal. And the earlier you can recognize your warning signs, the more gently you can support yourself.
In this conversation, we cover
Gentle reminder: you’re not failing. You’re carrying a lot, and it makes sense that your body gets tired of holding it.
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If you have ever heard “they can’t communicate” and felt your stomach drop, this episode is for you.
Because communication is not a performance. It’s a connection. It’s a regulation. It’s being understood. And when we only count spoken words, we miss the ways autistic kids communicate all day long.
In this conversation, we reframe what communication actually is, talk about AAC in plain language, and share how to support non-speaking, minimally speaking, and situationally speaking people with more respect, more curiosity, and way less assumption.
Today on Neurodivergent Conversations, I’m joined by Becky, a Speech and Language Therapist and Clinical AAC Specialist with Smartbox Assistive Technology, and we are going there in the best way.
This episode is packed with the exact kind of clarity parents and educators need, including:
If you are searching for support with autistic communication, AAC strategies, minimally speaking autism, or neurodiversity-affirming speech therapy approaches, this episode will give you language, hope, and next steps you can actually use.
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Smartbox Assistive Technology
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What if you are not “too much,” “too chatty,” “too sensitive,” or “just rude”
In this episode, we talk about what it feels like to be diagnosed with ADHD later in life, the quiet shame so many women carry, and the surprisingly practical supports that can change your day-to-day.
Today on Neurodivergent Conversations, I’m sitting down with Lisa, who was encouraged toward her own late ADHD diagnosis through her daughter Michelle’s journey, and who now leads Lexie’s Voice, a nonprofit supporting families touched by autism and developmental disabilities.
We chat about:
You will leave with language for what you have been experiencing, and a few gentle ideas you can try this week if your brain is always five steps ahead of your body.
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Check out the refreshed website
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Marriage can feel hard for so many reasons… and when you’re in a neurodivergent household, it can feel like there are extra layers you can’t always name.
In this solo episode, Greer shares a very honest snapshot of her marriage: she has ADHD, her husband is autistic, and they’re raising an autistic/ADHD child (with another little one whose “brain type” they’re still learning). She talks about the real stress points, the growth they’ve fought for, and the small “language tools” that have made communication feel safer and more doable.
Greer also opens up about a turning point from about five years ago—when she was close to leaving—and what helped them start repairing: individual counselling, marriage counselling, and learning how their brains work.
Why marriage can feel especially heavy in an ADHD/autism relationship
How miscommunication often comes from what wasn’t said (or how something landed)
The difference between being near each other… and actually feeling connected
Practical phrases that reduce conflict (like “10 minutes to dream” and “10-minute tap out”)
Why scheduling hard conversations can help neurodivergent nervous systems feel safer
How “survival seasons” can look like couch time—and why that can be okay (for a while)
A gentle reminder: you’re on the same team, and you’re not alone
If you’re in a season where it feels like you’re roommates, not partners—there’s no shame in that. You’re carrying a lot. This episode is your reminder that help is allowed, connection can be rebuilt, and sometimes the first step is simply finding words that work for your brains.
Learn about the Exhausted to Empowered Collective
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If you are in a neurodivergent relationship we are doing a webinar talking about the everyday realities. The joys and challenges while being or being married to a neurodivergent person. Join us Feb. 12, at 8pm UK, replay is available!
What if the thing that feels impossible, moving countries with a sparkly-brained kid, could actually become the start of your child feeling more supported, more understood, and more free?
In this episode, we talk about the kind of preparation that helps autistic kids feel safe in big change, how to keep the vibe hopeful even when the logistics are a lot, and what it looks like to build community when you are new, anxious, and navigating a language barrier.
Today on Neurodivergent Conversations, I’m joined by Alexis Nicole from Mommashive, a travel and lifestyle creator living in Portugal after relocating from the United States with her family.
We get into the real, practical stuff you actually want when you are considering a move or a big trip with an autistic child, like:
This one is especially for the parent who is thinking, “I want to give my child more world, but I’m scared I’ll make everything harder.” You are not alone, and you are not the only one doing a ton of prep behind the scenes.
GUEST LINKS:
Follow Alexis over at Mamashive on Instagram
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Check out the refreshed website
Learn about the Exhausted to Empowered Collective
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SPONSOR LINKS:
Check out ADHD Central and their great tools!
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JOIN US FOR A WEBINAR for Neurodivergent Couples. Happening online February 12 at 8PM UK. Replay is available.
Ever feel like your brain is sprinting, even when you are sitting still?
Today on Neurodivergent Conversations, I’m joined by Graham, an author (including Babies Don't Talk), entrepreneur, and one of the humans behind ADHD Central, a brand analog supports for ADHD brains.
We chat about the real, everyday stuff that so many late-diagnosed adults quietly carry, like:
If you are navigating adult ADHD, neurodivergent just craving tools that feel doable, this one is going to land.
GUEST LINKS:
Follow ADHD Central
Check out their resources
GET THE LINKS
Check out the refreshed website
Learn about the Exhausted to Empowered Collective
Follow me on socials:
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Learn more about your ad choices. Visit megaphone.fm/adchoices
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