
A grown man wrestling a duvet cover turns out to be a surprisingly accurate metaphor for what happens when children with EBSA and neurodivergence are expected to navigate a school system that assumes they instinctively know the rules.
My husband cannot make a bed.
I don’t mean he’s a bit slow at it, or that he folds things in a vaguely abstract, modern-art kind of way. I mean he genuinely, spectacularly cannot put a duvet cover on. It has reached the point where I no longer ask. It’s better for both of us.
Over the years I have found him, on more than one occasion, physically inside the duvet cover. Not metaphorically. Actually in it. Arms flailing, fabric twisting, face peering out of the opening like someone attempting escape from a soft, floral prison.
Most people know how to put a duvet cover on. You’re expected to just… know. No one teaches you. You absorb it. You figure it out. And if you can’t?
Well, it’s “not that hard,” is it?
That’s when the joke stopped being just a joke.
Because I started to think about the children we work with—particularly those experiencing EBSA, and those who are neurodivergent.
And I wondered: What if school feels like that duvet cover?
From the outside, the system looks logical. Structured. Predictable.
You go in, you sit down, you learn, you revise, you sit the exam.
There are choices, different schools, subjects, pathways, but ultimately everyone is expected to reach the same endpoint. A system that, much like the duvet cover, looks simple if you already know how it works.
But recent conversations in education are starting to acknowledge something important. For many children, particularly those with ALN/SEND, the system hasn’t just been difficult. It’s been unworkable.
The government itself has described the current system as one that has “failed… too many children,” with families forced to fight for support that often never materialises in practice. And when you listen to the young people we work with, that rings painfully true.
Because for children experiencing EBSA, school isn’t just a place of learning. It can feel overwhelming, unpredictable, and unsafe. The noise, the expectations, the social demands, and the pressure to perform, it all builds. And from the outside, what we see is absence.
But from the inside? It’s panic. It’s shut down. It’s tangled up in something you cannot navigate, while people outside say, “Just come in. It’s not that hard.”
For neurodivergent children, the experience can be just as disorientating.
They are often expected to navigate:
- Unspoken rules
- Fast-paced verbal instructions
- Sensory-heavy environments
- Abstract expectations about behaviour and learning
All without those things ever being explicitly taught. The system assumes understanding.
But assumption is not the same as access.
And this is where the current ALN/SEND reforms start to matter. Because, on paper, they are trying to address exactly this gap.
There is talk of moving away from a “one size fits all” model. Of introducing Individual Support Plans for every child with ALN/SEND. Of training all teachers, not just specialists, to adapt how they teach. Of creating “inclusion bases” within mainstream schools for children who find the environment overwhelming.
There is investment, billions in fact, into specialist support, early identification, and services like educational psychology and speech and language therapy.
And that sounds promising.Because, in theory, it suggests a shift. From expecting the child to figure out the duvet cover…to changing how the duvet is held in the first place.
But there is a tension here because alongside that vision sits another reality.
Families and organisations are already raising concerns that, without enough capacity and clarity, these plans risk becoming resource-led rather than needs-led. Questions remain about whether support will actually be available when it’s needed. Whether Individual Support Plans will be meaningful, or just another document. Whether reducing reliance on formal plans like EHCPs could weaken legal protections for the children who need them most. And perhaps most importantly whether the system will truly adapt to the child or whether the child will still be expected to adapt to the system.
Because if we’re honest, this isn’t a new problem.
The ALN/SEND system has been under strain for years. Demand has risen sharply. Outcomes for these pupils remain significantly lower than for their peers. And in that context, it’s not hard to see how children, especially those with EBSA or who are neurodivergent, end up feeling exactly like my husband inside that duvet cover.
Confused.
Frustrated.
Increasingly aware that everyone else seems to be managing something they cannot.
So what do we do with that?
Because this isn’t just about policy. It’s about perspective. The reforms talk about inclusion and early support. About making help available “without a fight”. But inclusion isn’t just about placing children back into the same system with a few adjustments. It’s about recognising that for some children, the system itself needs translating.
Breaking down the steps.
Making the invisible visible.
Slowing it down.
Changing the environment, not just the expectation.
Because I’ve learned something from all those moments of finding my husband tangled up in a duvet cover.
From the outside, it looks simple.From the inside, it isn’t.And no amount of shouting instructions from across the room will fix that. What helps is something much quieter. Someone stepping in.Turning it the right way round. Showing, not telling, where the corners are.
If these ALN/SEND reforms are going to mean anything for the children we work with, for those experiencing EBSA, for those who are neurodivergent, then that’s the shift they need to make real.
Not just more structure. Not just more plans. But more understanding. These children are not failing the system. They are doing their best to navigate something that was never designed for them.
And until we truly see that, they will keep getting stuck… inside the duvet cover.
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