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Lauren Quirke

Founder & Lead Consultant

Lauren is the founder of Somenté and works directly with parents raising neurodivergent children. With a background in neuro rehabilitation and a Master's degree in clinical exercise physiology, she brings a neuroscience-led lens to understanding what's actually happening beneath a child's behaviour — working alongside families' existing clinical teams, rather than in place of them.

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"How do you do that? I could never get them to do that." It is the question I hear more than any other, usually from a parent watching their child attempt something in a session that they have never once tried at home. My answer is always the same, and it always surprises people. It was not the activity I chose, and it was not a technique I had that they didn't. It had nothing to do with being a specialist. It was that I started somewhere completely different, somewhere that most parenting advice never reaches at all.

Where most advice starts, and why it keeps failing

The parenting space for neurodivergent children is saturated with strategies: what to do when everything falls apart, how to structure the morning routine, which approach to use for homework resistance, how to get through the hard moments in public. If you are raising a neurodivergent child, you have almost certainly worked your way through a long list of them, and if you are reading this, some version of that list probably has not stuck. I want to suggest that the question worth asking is not which strategy to try next, but why none of them are holding. In almost every family I have ever worked with, the answer is the same: the strategies are being introduced into a nervous system that has not yet been given the conditions to actually receive them.

What has to be true before anything can change

Here is what years of working directly with neurodivergent children have taught me. No meaningful, lasting change happens in a child who does not feel safe, not safe in the physical sense, but safe in the neurological sense. Stephen Porges, in his polyvagal theory, calls this process neuroception: the nervous system's constant, subconscious scanning of the environment for cues of safety and threat, running well beneath awareness and long before conscious thought. Your child is not deciding whether they feel safe. Their nervous system is deciding for them, moment by moment, based on signals neither of you may be consciously aware of. A child whose nervous system is reading the environment as threatening, or reading themselves as a problem, is a child whose capacity to absorb new information, build new skills, or trust the process is fundamentally limited. This is not a philosophy so much as a neurobiological fact. Neuroplasticity, the brain's ability to form new pathways and responses, requires very specific conditions, and those conditions are not met under stress. The neuroscientist Amy Arnsten at Yale University has shown that even mild, uncontrollable stress rapidly impairs the prefrontal cortex, the part of the brain responsible for learning, sequencing, and building new skills. When a child's system is operating in protection mode, the capacity for new learning is not merely reduced; it is functionally unavailable. You can introduce the activity, you can use all the right words, and the skill will not transfer.

This is the loop so many families are stuck in, and I suspect you will recognise it. The approach that worked for a week before it stopped. The morning routine that held until one small thing changed and everything unravelled. The thing that every article promised would work, and briefly did, and then did not. You try something, it holds for a few days, and then you are back to square one; you try something else, and the same thing happens. The missing variable is almost never the approach itself. It is that the nervous system it is being introduced to has not yet been given what it needs to actually hold new learning.

This is also why the same child can be entirely absorbed in something they love for three hours and completely unable to begin a single step of something else five minutes later. It is not inconsistency, and it is not defiance. It is a nervous system whose available capacity shifts with what it is being asked to do and, crucially, with how safe it feels doing it. For many of these children, emotional intensity arrives fast and at full volume, while the recovery from that intensity is far slower and more costly than it looks from the outside. So this is where I start, with every family, before anything else.

What your child is actually sensing

Neurodivergent children are often extraordinarily sensitive to the emotional environment around them. Their nervous systems frequently process relational and emotional cues at a higher intensity than those of neurotypical children: they pick up on tone before words, they read body language before they read the sentence, and they feel the energy in a room long before they have any language for it. This maps onto something communication research has understood for a long time, that the relational meaning of a message, whether we feel accepted or judged, safe or unsafe, is carried far more by the nonverbal channel of tone and body than by the words themselves. We can control our words. We are far less able to control everything underneath them, and it is everything underneath them that a neurodivergent child reads first. Which means they can feel it when they feel like a problem.

I have watched this happen in real time, in session after session. A parent who flinches slightly when their child stims in public. A parent who feels a pull of discomfort when their child's way of being in the world, their movement, their communication, their reactions, stands out in a crowd. A parent who is exhausted, trying everything, and still carrying a layer of grief about who their child is; not because they love them any less, but because this is genuinely hard, and grief is a real part of that experience. None of those parents are doing anything wrong, and all of them love their children deeply. But the child is reading it, and what the child is learning, quietly and early, is that who they are creates discomfort for the people they love most.

It is worth pausing here to ask yourself a question that requires real honesty, because I ask it of every parent I work with. When your child does the thing that draws looks, the stimming, the volume, the moment everything becomes too much in the middle of the supermarket, what happens in your face and your body before you say a single word? Not what you say. What you signal. Your child already knows the answer, and they knew it long before you did.

I want to share a moment that has stayed with me. I had been working with a child for nearly two years. He was eight years old, and we had built a great deal together: his regulation vocabulary, his ability to read his own body, the tools he reached for when things got hard. One day I asked him whether his parents did the deep pressure squeezes with him at home, the same ones that settled his nervous system in our sessions. He said no. When I asked why he had never shown them, he thought about it for a moment and then said: because I don't want to embarrass them. He was eight years old, and he had already decided that his sensory needs were something to carry quietly, to protect the people he loved most from the discomfort of seeing them. That is what shame does. It does not reduce the need; it removes the outlet and adds weight to the load.

This sits inside a broader pattern I see in almost every family I work with. Many neurodivergent children hold themselves together through the environments that feel demanding, school, social situations, anywhere performance is required, and then release all of that held tension the moment they walk through the front door. What a parent experiences as their child falling apart at home is not home being the problem. It is home being the one place safe enough to finally let go. The collapse at home is evidence of trust, and it deserves to be understood as such: not managed, not corrected, but received.

The shift I ask every family to make

The most powerful thing you can do for your neurodivergent child is not a technique. It is a shift in how you understand them, not just in theory, but in the felt sense; in the way you speak about them and the way you respond to them in the small, unremarkable moments of an ordinary day.

This is what I call the neuroaffirming foundation, and it underpins everything in my practice. It means understanding and affirming how a child's nervous system actually works rather than working against it. It asks you to move away from the belief that your job is to help your child fit into the world as it currently exists, and toward genuinely understanding your child's world first, so that navigating the wider world becomes sustainable for who they actually are.

In practice, this looks like specific things. It looks like letting your child wear their headphones in the supermarket even when it draws looks, because their sensory safety matters more than the perceptions of strangers. It looks like speaking about their differences with genuine curiosity rather than frustration or apology, and celebrating how their brain works rather than quietly wishing it were different. It looks like believing, with real certainty, that they are not behind, they are not broken, and they are not a problem to be solved. They have a nervous system with specific needs, and they are entirely capable when those needs are met. None of this is about lowering your expectations of your child. It is about understanding what they actually need in order to meet them.

Why your regulation is part of theirs

One of the most important things I share with every family I work with is this: your nervous system is one of the most powerful regulatory resources your child has access to. Co-regulation is not a therapy technique; it is a neurobiological reality. Longitudinal research by Ruth Feldman, tracking families across the first ten years of a child's life, has shown that parental responsiveness and child emotional regulation are bidirectional and mutually reinforcing. A regulated, attuned caregiver directly supports the development of a child's own capacity to regulate. A calm, settled nervous system lends steadiness to one that is overloaded. When you are regulated, genuinely settled rather than suppressing your stress, your child's nervous system has something to borrow from. And when you are dysregulated, even if you never raise your voice, they feel that too. Think of the tense school run where you have not slept, have said nothing, have done nothing wrong, and your child is already harder to reach before you have left the driveway. That is not coincidence. That is co-regulation working in both directions.

This is not a demand for perfect calm. No parent is calm at all times, and that is not the expectation. What matters is understanding that your own state is not separate from your child's experience; it is part of it. The environment you hold, which includes you, is among the most powerful influences on how much capacity your child has available to grow.

And the environment you build at home shapes what your child can access everywhere else. A child who feels genuinely understood and accepted develops something that travels with them: self-awareness about what their nervous system needs, and a growing capacity to move through difficulty without it becoming evidence that something is wrong with them. Things can still be hard. But they have something real to build from, and that foundation does not stay at home.

Why this work always comes first

The presenting challenges are real. The school struggles, the sensory overload, the emotional dysregulation, the executive functioning difficulties are all real, and all of it deserves careful attention. And beneath all of it, these children are working significantly harder to get through an ordinary day than anyone around them realises. That effort deserves to be seen too.

I also want to be honest about scope. The neurodivergent spectrum is wide, and the complexity of what is happening in some children's brains and bodies should never be underestimated. There is a significant difference between a child who struggles to make friends and a child whose regulation needs are extreme, or whose sensory-seeking is physically distressing or risky. I am not claiming that building the foundation described here is the complete answer for every family. For many, the picture also includes occupational therapy, psychology, speech pathology, and other specialist input that is essential and irreplaceable. What this foundation does is make every other form of support more effective once it is in place. Somenté works alongside the specialists in your child's life, not instead of them.

But none of it shifts sustainably unless a child fundamentally believes that the people around them see them as extraordinary, not in spite of how their brain works, but including it. A child carrying shame about who they are cannot take in feedback, cannot build self-belief, and cannot tolerate the discomfort of working on hard things, which all real development requires. A child who feels genuinely seen and safe does all of those things with a willingness that can be remarkable to witness.

This is why, in my work with families, building this foundation is always the starting point. Not because it is the most obvious thing to address, and not because it is the thing parents usually come asking for. Most parents come wanting to know what to do. The answer, which I have watched hold true across every child I have ever worked with, is that what you do next matters far less than the relationship in which you do it. The change you are looking for starts here: in your understanding of your child, in your home, in the twenty-three hours that no specialist is present for. When it starts here, everything that follows has a foundation to actually stand on, and the progress you have been working so hard toward, the change that has felt just out of reach, begins to hold.

A note from Lauren

Every parent who finds this article has come here through a different road. Some of you have been navigating this for years, carrying more than most people around you know. Some of you are just at the beginning, still trying to understand what is actually happening for your child. Some of you are somewhere in between, with a picture that is starting to form but still has pieces missing.

Wherever you are, you came here because you are trying to understand. That is not a small thing.

This article is not the complete answer. Nothing in a single piece of writing can be. But if something here felt true, or put words to something you have been quietly knowing, I hope it gives you a little more to stand on.

If you would like to understand what this looks like for your family specifically, I offer a free 30-minute conversation. No agenda except to get the real picture of what is happening for your child, and to talk about what changes when you start there.

I would love to hear from you.

Lauren

References

Arnsten, A. F. T. (2009). Stress signalling pathways that impair prefrontal cortex structure and function. Nature Reviews Neuroscience, 10(6), 410–422. https://doi.org/10.1038/nrn2648

Feldman, R. (2015). Mutual influences between child emotion regulation and parent-child reciprocity support development across the first 10 years of life: Implications for developmental psychopathology. Development and Psychopathology, 27(4), 1007–1023. https://doi.org/10.1017/S0954579415000656

Porges, S. W. (2007). The polyvagal perspective. Biological Psychology, 74(2), 116–143. https://doi.org/10.1016/j.biopsycho.2006.06.009

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