Saying the SEND system is in crisis is no great reveal; it is proving ruinously expensive while failing to deliver either improved experiences or outcomes.
One consequence of its long-term failure has been great antagonism between families and schools, with the idea parents must fight tooth and nail for the support their child needs now regarded as a fact of life.
This belief is now so well established I am concerned it is spreading out of the SEND system and becoming a feature of school life in general.
Parents may be coming to believe they are letting their children down if they don’t fight for extra support for them regardless of how well they are doing in school.
This is a quite understandable thing to do and not new.
Many parents who can afford to do so have always sent their children to private school and many others for whom this is too expensive pay for private tuition to try and secure their children extra advantages.
The new problem we have is we are now conceptualising a failure to achieve as well as others on a quite average range as evidence of specific learning difficulty or disability, with many families now believing they let their children down if they do not find them extra support to help boost their performance.
The first problem with this is that we grade children by comparing them with others, which means this becomes an arms race – to reach the top you must outcompete others; if they are getting extra help then you must get your child the same or more help if they are to remain competitive.
The second issue is this sort of thinking makes not being at the top of the class a medical problem rather than an inevitability for most people.
“She’s working so hard,” a parent might say, “but she’s only getting 3s and 4s. We feel this isn’t what she should be getting for all of that. Can we investigate whether there’s something that’s holding her back?”
Here often begins the route to some sort of diagnosis, informal or formal, and then theoretically additional support that should address the issue and restore morality.
If the support available did lead to better learning, then this might not be a problem.
But does it?
Do movement breaks and fiddle toys, coloured paper and wobble cushions, mental health interventions and other well-meaning strategies boost attainment?
The evidence for these rarely disprove the null hypothesis.
So why do we persist? Why do we layer on more and more of these ineffective things and pretend they’re doing good when we usually have so little evidence they are?
I fear the answer is because we’ve made “additional” the point rather than looking at the evidence of what is likely to help. This might be because what really works is usually what works for everyone – things like overlearning, reading, homework and practice; hard, effortful, unglamorous work that takes a long time that probably won’t rocket you to the top of the class regardless of how diligent you are.
Facing this, it’s easy to see why the snake-oil is so tempting.
And it’s also important to say here that when practice is dubious families often don’t know this – they have no reason to believe what they have been told by those in authority isn’t true, which makes their frustration and concern entirely understandable. What must it be like to worry about your child struggling and then hear another child with comparable difficulties is receiving a raft of strategies and interventions your child isn’t getting?
Recently at a conference I got talking to a SENCO about the poor state of evidence for the sorts of strategies commonly suggested by educational psychologists, other teaching-adjacent professions and increasingly, the internet.
“Oh, I know,” she said, “but they (the parents) come in expecting something extra and they won’t leave without that. Sometimes I just have to give them something to protect the relationship. Otherwise, they’ll just make a complaint.”
We then talked more about why her job was so hard – about all the pressures that existed that made her feel she had no choice but to implement things she did not agree with and knew were of no use at all.
Because “additional” may have become the point with whether it works or not reduced to an afterthought.
Two years ago, at a conference I described the process my wife and I went through to get our daughter her EHCP.
I used a phrase familiar to those of us with children who find life harder and need more help – those often identified as having a special educational need – common advice given to parents when filling in forms about their child’s struggles.
Some of you might know it too.
“Describe her on her worst possible day,” we were told, “otherwise they’ll say you’re fine and you won’t get anything.”
I looked up and saw three people in the audience crying.
Three experienced teachers and school leaders in their conference smart-casual openly weeping over their specially bought stationary.
I knew why at once – it was because they were parents as well as teachers.
They knew what those words meant, not just professionally but personally too.
They knew what it felt like to be asked to describe a beloved daughter “on her worst possible day.”
Imagine if you had to do this for your child when they first started school.
Imagine being made to write all their lowest moments, their failings, their embarrassments and their intimacies on a piece of paper for someone you don’t know to read and judge.
Imagine the shame and the humiliation.
If you’ve never had to, and you can’t imagine, let me help.
It’s dreadful.
I’ve cried myself.
Once – memorably at my desk at work when I opened a screening questionnaire about my wonderful then five-year-old to find a question asking me, as her dad:
“Does she talk for long periods of time about things nobody else is interested in.”
I blinked back hot, angry tears and then then baring down so hard on the paper with my pen I almost broke it wrote, in capitals.
“I AM ALWAYS INTERESTED IN WHAT SHE HAS TO SAY.”
This is the deficit model and what it does. It makes parents like me cry.
It makes the price of help failing first and then having to share those failures as if making confession.
It makes humiliation the price of support.
What must this feel like for the most vulnerable children in our schools, those already made acutely aware they are falling behind their classmates every time they do so much as a quiz?
Why the indignity?
Why are things organised this way?
This is impossible to understand without first understanding how many features of modern society are based on the medical model, which aims to find problems and then fix them – to diagnose and then treat.
On its own terms the medical model has been enormously successful with millions of people across the world living longer, healthier lives because of it.
We need it.
I do not want to go to a doctor with a serious illness and be told unpleasant symptoms are a positive feature of my identity which need to be affirmed, or something I must simply endure because they are an inherent part of who I am.
If I am ill, I want someone to find out why and then cure me.
But the medical model is of no use – even dangerous – when applied to people who are not diseased.
And a person with – for example – a learning disability is not ill, broken or deficient.
Finding learning to do things harder than others is an aspect of their humanity and should not be a source of fear or shame.
There is nothing inherently wrong with someone who finds things hard to do, but to help them with these things the orthodoxy requires us to medicalise them – to construct them as deficient or poorly so they can receive the correct treatment.
For example – for a child to get extra help with reading they must first fail at it, which might then allow for a diagnosis of dyslexia, which should – theoretically at least – lead to corrective interventions or adjustments. Similarly, a child who struggles to focus and concentrate must fail at things because of their difficulty before receiving a diagnosis of ADHD which again – theoretically at least – should get them the support they need to be successful.
This can be an unpleasant, even undignified process but perhaps it is worth it if it results in better experiences and outcomes.
But this framing and the associated processes are not improving much at all.
Despite identifying increasing numbers of children with specific educational needs requiring extra support and spending increasingly vast sums, at scale neither outcomes nor experiences are improving, and we are amid a system wide collapse that will hurt our most vulnerable children most.
Why are things so bad?
The first reason is many of the diagnoses we use in education are of little use to those who get them, because even when there is consensus around the meaning of the diagnosis itself they are catch-all umbrella terms that can easily lead to stereotyping.
Williams Syndrome – which my daughter has – is a good example.
While there is no doubt of WS’s biological origin and cause – a microdeletion of genes on chromosome seven – the people who carry this difference are very different to each other.
Some are non-verbal and need lots of help to look after themselves.
Others can read and write just as well as most people their age.
Some have great musical talent and play instruments in professional orchestras.
Others have little musical talent but love to sing and dance.
The range of characteristics is just too wide for the diagnosis to give any more than the broadest of steers on what a school should do for children with the condition – and we can’t even know what characteristics are caused by the genetic difference and what are caused by other genetic and environmental factors.
Does it even make sense to say anything people do is a result of their condition given a condition is inherently part of them anyway?
Is Bessie’s love of music because she has WS?
Or is it because I love music too and have always listened to it with her since she’s been a baby?
Is it both? Is her love of music her WS or just her? Is there a difference? Does trying to make a distinction make any sense at all? Does it even matter?
To begin with when we began working with researchers and learning scientists we thought – perhaps even hoped -we would find special ways of learning that would allow Bess to make faster progress, but we soon learned things don’t really work that way.
There are no hacks.
While Williams Syndrome has some consistent features, the way those with it learn is basically the same as those who don’t.
Struggling with reading? Phonics and lots of practice.
Struggling with numeracy? Manipulatives and lots of overlearning of the basics.
Struggling to pay attention? Limit distractions and build this up progressively.
Everything I’ve read suggests this is true of just about everybody – while the extent of struggle might be different what helps is usually more of what know works for everyone, just done better.
And this brings us to an important point.
Finding learning harder for whatever reason – even where this has a genetic cause – is not a deficit. Someone who finds learning hard is just as beautifully human as someone for whom it’s a breeze.
Nothing has gone wrong.
There is nothing to fix.
There is nothing to cure.
Even if we wanted to change Bessie – which we don’t because that would mean trading her for a hypothetical someone we don’t know – we couldn’t and, by trying, we would signal to her she isn’t good enough as she is, which is heartbreaking to even think about.
But, sadly, I think society does this to a lot of people because our values are underpinned by the meritocratic myth – the idea everyone starts at the same point and what we end up achieving in life is down to how hard we try.
Think about how we celebrate those who achieve the most – famous actors and musicians, millionaire entrepreneur businesspeople, politicians and global leaders. We honour them because we – as a society – choose to believe they are worthy of our admiration because of personal qualities we should all aspire to and have the capacity to emulate.
Is this true? Do the highest in society rise to their positions because they deserve to?
Sometimes? Maybe.
Usually? Probably not.
Always? Certainly not.
And this is profound because an unpleasant inverse of this aspect of the meritocratic myth is those who fail to reach such heights – most of us – must accept this is because they are less competent, less able, perhaps simply less good than those who do.
This framing – and the associated deficit model – makes a failure to be good at something a source of shame and worrying about not being good enough a source of understandable anxiety.
Might this be a driver of the recent uptick in the number of young people diagnosed with conditions such as ADHD and ASD?
Perhaps it might.
It would be logical for those struggling to feel successful to look for medicalised reasons for their difficulties, especially if they believe there are interventions and treatments available that can help, and especially if they’re feeling pressure to be productive and achieve things they doubt their capacity for.
Here, it is important to be clear about the difference between medical diagnosis and the sorts of diagnosis more common in education – a poorly understood difference explained well in Professor Timini’s recent book “Searching for Normal.”
Timini explains diagnoses like ADHD are tautologies because they are descriptions of symptoms which say nothing about the cause – like saying someone has got a headache because their head hurts – this means they tell us little about what causes the condition.
This does not necessarily mean a diagnosis isn’t real or helpful.
There are many conditions – for example migraines and schizophrenia – that are also tautologies and are no less vital for being such.
But it’s important to understand every diagnosis is a medical process which creates a deficit model because to say someone has a “disease” or “disorder” is to say there is something wrong with them that requires fixing.
Perhaps surprisingly the popular view this is true is not supported by evidence.
While received wisdom often holds conditions such as ADHD and ASD have biological markers – for example gene variants of chemical imbalances – while this is often asserted and studied, no study has shown this to be true, which is why diagnosis of these remain tautologies. This – for reasons I haven’t time to get into today – is often not as clear as it should be.
For example, the NHS says “The cause of ADHD is not always known. ADHD may be caused by genetic differences.”
I don’t like this phrasing very much as it disguises the truth – no study has ever found anything biological that causes the condition despite huge amounts of time and money being spent trying.
This would not be as much of a problem if it was better understood why tautological diagnoses are very different to purely medical diagnosis; that they don’t lead to proven effective treatment or medical management in the same way.
This is now being discussed more and there is growing unease that instead they are problematising and medicalising normal human behaviours and creating deficits where none existed before – making people who are no unwell think that they are.
But, nonetheless, these diagnoses are valued by many who receive them.
Many people who receive a diagnosis for a condition with no proven medical cause say they find it useful and affirming because it helps them understand why they find some things harder to do than others where before they were regarded as being lazy, disorganised or plain stupid.
Families often report finding the diagnosis of their children helpful because it makes them feel they understand them better.
This is understandable.
Different people do find things harder or easier than others for reasons beyond their control and victim blaming – telling them their suffering is their fault – is both untrue and cruel.
Many also feel a lack of evidence for a medical cause for a condition does not prove there isn’t one – only that the cause has not yet been discovered.
If this is true – and of course it might be – then waiting for such evidence to be discovered before finding ways to help would be irresponsible because while we wait, thousands of children will not be helped.
Some go further and argue advances we have made in understanding neurodiversity have exposed problems the traditional model for schooling simply cannot cope with.
These people argue that for many years those who struggle in school have had no choice but to struggle on, hiding and masking their suffering to fit into a system inherently hostile to them – the development of new diagnoses and the expansion of existing ones has given people the language they need to explain their struggles and challenges and is protective of their dignity because it makes these things part of their identity rather than shameful moral failings.
I have no doubt this affirmative model of difference has helped many people – giving them back a sense of dignity by providing terms and language allowing them and others to see their struggles and difficulties as not moral deficiencies but evidence they face more significant challenges than others.
There is a profound and important truth in this.
While we do – as is often pointed out – all have the same numbers of hours in a day our days are not the same and we do not all start from the same point. To achieve the same things some must struggle harder than others and it is good to be always mindful of this to protect the dignity of those with less privilege and to check the hubris of those who have more.
We must also take care not to gaslight the very real struggles and even suffering of those finding school hard. We live in a flatlining economic, post-manufacturing world in which it has never been as important as it is to do well in school as it is now.
The parents of Generation A and Z are the children of Blair, told that Education, education, education was the path to wealth, meaning and fulfilment.
So many more jobs require degrees.
There are fewer and fewer second chances and jobs that require no qualifications have never been so insecure or undignified.
All of this on top of an endless flow of Instagram posts and TikTok videos implying the entire world is happy, attractive and endlessly productive.
It is hardly a mystery many people are looking so hard for reasons they don’t feel they are keeping up and looking for explanations and helpful strategies.
But – as well-meaning as it may be – the process of diagnosis and intervention is not without risks and potential trade-offs.
Firstly, because it reinforces the idea that the only way to have value is to be productive and those who are less productive are of less value.
This is inherently ableist and condemns huge numbers of people to inevitable failure.
Secondly, a diagnosis of a special educational need does not definitely mean a child will receive better provision – indeed the results of a recent SchoolsWeek investigation suggests that in many cases it might make things worse.
The investigation – into the contents of Section F in EHCP documents – revealed some horrifyingly dubious practice including programmes such as “Squiggle While You Wiggle” and even teaching children to their “preferred learning style” – a practice that has been comprehensively debunked and driven out of mainstream education.
Efforts to help those who find things more aren’t dignified if they don’t help, regardless of good intentions.
I do not want my daughter – or anyone else’s child – dancing in a corridor, sitting in a sensory tent or rubbing her hands in sand and water based on a hunch or a badly constructed study that has never replicated.
Secondly, diagnosis and the potential construction of deficit in children may result in diagnostic overshadowing and something I’ve only quite recently become aware of – the nocebo effect.
Diagnostic overshadowing is what happens when people assume the characteristics or behaviour of a person with a diagnosis is the cause of what they do and think, when it might be a completely unrelated environmental factor.
A good example of this might be the assumption a child is not making progress in reading because of dyslexia when the main and most important cause is they aren’t doing any practice at home.
Here, assumption can easily become a low expectation, which can then impoverish the educational provision they receive – these easily become dangerously self-reinforcing too – as in “Ash has dyslexia, so we won’t push him too much on his reading at home – he’s always going to find this difficult.”
This can then create a negative feedback loop whereby the diagnosis – in this case dyslexia – removes opportunities for the recipient of the diagnosis to improve at the thing they struggle with.
There is also danger in believing a child’s diagnosis is a fixed, immutable condition that must be accommodated because it can’t be cured or meaningfully ameliorated.
As well-meaning as this might be it can also be disabling if more and more concessions and adaptations are made and the child and their family come to believe they cannot do without them.
What was intended to be a scaffold can turn into a cage.
And it can be very hard not to fall into this cage because of the Nocebo Effect.
Nocebo is placebo’s evil twin – it is when a person develops new symptoms, or existing ones worsen purely because of the belief they have a medical condition regardless of whether they do or don’t.
I think this is so common as to be unremarkable.
It certainly happens to me, and I suspect it happens to us all to a greater or lesser extent.
Recently, for the first time after coming across a reference to them on an online running magazine, I became aware of a very mild bunion on my left foot. Ever since, I feel discomfort and even a slight pain when wearing some shoes. Even though I know – rationally – that it is deeply implausible this discomfort and pain developed at the exact same time I noticed the bunion I can’t shake it. Even though I know my symptoms have most probably developed psychosomatically, they are real to me and very annoying.
It is very possible something like this might happen to at least some children receiving tautological and descriptive diagnoses and associated “treatments” and interventions.
If a child is told they have a medical condition such as ADHD, is there a risk that this could then worsen their symptoms as they learn more about them? If a child is told they read better with green paper, overlays or lenses could they then find it harder to read black text on plain white paper? If a child is told they have a sensory processing disorder, is it possible their symptoms worsen as they become more aware of them?
Why was this?
Before going on it would be unfair not to acknowledge there are some who strongly argue that the development of new symptoms and the worsening of existing ones are not psychosomatic but real existing ones revealed by a process called “unmasking,” in which a person stops suppressing aspects of their personality as they become more confident and comfortable.
It is possible this is true, and it is of course also possible both nocebo and unmasking could be happening at the same time.
Evidence for both these claims – of nocebo and unmasking – at present might well be inconclusive either way, but this does not mean we should dismiss the possibility of either – this would be just as irresponsible as saying that – for example – in the absence of definitive proof head injuries in rugby might cause cumulative brain injuries we should make no changes and take no precautions.
Being responsible means considering all possibilities – we should not shut down conversation about any possibility when we aren’t certain what the truth is.
So, what should we do?
As always, pointing out problems is much easier than finding solutions.
What is the best approach to protecting the dignity of the most vulnerable children?
How do we best help young people experiencing extra difficulty without problematising them?
Before anything else we must acknowledge whatever our opinions about the medical – or quasi-medical – model the education system operates within we and the families we are responsible for have no choice but to play along.
As unpleasant as it often is, at present the only way children can get the extra support they need is to prove failure and without doing this they may not get any help at all – in these circumstances a diagnosis can be necessary as an explanation that then unlocks funding and other resource.
Even if we disagree failing to engage would be irresponsible because it would mean ignoring the real specific difficulties children are facing – we need to know what’s hard for them so we can help.
There are also limits to our agency – parents have the right to make medical decisions for their children and provision in Section F of EHCPs is a legal entitlement regardless of whether that provision is sound or not.
For what it’s worth, I think this is bad law but accept this is not a reason it is acceptable to break it.
So, what can we do?
I propose adopting one simple principle we could apply to all our work; every action has potential positive effects and risks.
By this I mean we must dismiss the assumption doing anything is better than doing nothing, and that we shouldn’t try things just because they are a thing to try.
We must not fall into the trap of “something must be done, this is something, let’s do that thing.”
I propose before anyone does anything we involve a wide range of people in deliberately and carefully thinking through these potential positives and potential risks.
For example, a dyslexia diagnosis might lead to improved self-esteem and access to helpful assistive technologies, but it might also lead to a sense of fatalism about reading that could conceivably limit progress.
ADHD medication may have the potential to improve academic focus leading to better results in tests, but it might also lead to dependency and progressively increasing doses to maintain the same effects.
Applying the principle properly would require us to look at individuals and contexts too, because these would have a bearing on the extent of potential positive effects and risks – this might require us to go beyond just education and into health too, which feels appropriate given the overlap we often experience in schools.
For example, if professionals did this, they might be slower to recommend amphetamines for ADHD to a child with a family history of either addiction or heart disease than they would for a child in a family without this.
Many decisions about diagnosis and treatment will rightfully remain in the hands of families rather than schools and here the role of teachers and leaders would be ensuring that these decisions are fully informed – that families have considered both potential positives and risks before deciding what they should do.
This could look like this:
“Yes, we could put in for exam concessions for Sophia based on this diagnosis, and some children say they have found this useful, but before we go for that as an option, I want you to be aware this would mean all her exams when it comes to the GCSEs would be longer, which means she would be in exams a lot more of the time. Could you have a chat with her about this is something you all still want to do?”
Or:
“We could give Tom pink resources as this optometrist has suggested, but before we look at that I want you to read this summary of studies which shows there is no evidence this helps beyond the placebo effect. I also want you to be aware we have seen children who report finding reading harder on white resources after they were provided with coloured paper than before. This might be because of something called the nocebo effect.”
I could go on, but I hope I’ve made my point – by exploring advantages and trade-offs over specifics we can have much better discussions than by getting into stand-offs over generalised and more abstract concepts.
Doing this right means being scrupulously professionally honest whatever paradigm you most fit into and adopting scout over soldier mode; claiming large numbers of children are being made mentally ill by normal school rules and routines would be as irresponsible as claiming a Ritalin prescription is an inevitable fast-track to illegal Class A drug addiction.
I hope by doing this we would evolve better more evidence informed conversations – and if we are to make any progress at all this is essential, because at present our systemic shared knowledge about special educational needs is dire.
Too few people know the differences between how different diagnoses are arrived at, or the evidence bases behind widespread intervention practice. There is far too much of “let’s just try this and see what happens” and far too little honest and open impact analysis.
Too few people understand why the structure of different studies matters so much or even why debate is so charged and angry.
This might feel damning, but I don’t think it is controversial among teachers and school leaders who regularly say the aspect of their jobs they are least confident about are those to do with educating those with special educational needs and disabilities.
We must do better, and this means learning more and this also means being brave – in not just accepting something as being true because someone has told us – even, especially, with confidence it is true.
This I know – at present but I hope this will change – feels like going against the grain.
It concerns me that even asking questions like I’ve done today feels professionally risky – that many people feel unable to do the same not because they fear strong opposing arguments but because they fear the fury and rage of those who disagree with them. It concerns me that my positionality – as in being the parent of a child so directly affected by this – is why I feel I have more agency to talk about this than others who are far better qualified to do so.
It concerns me we call those most tasked with the education of those with the greatest challenges “co-ordinators” and not leaders, because it implies their role is to do what others tell them to do without question – to accept on faith the advice they get is both sound and appropriate.
The best SENCOs I know do not do this – they are respectfully sceptical – they question and interpret, challenge and support, even when they know this is likely to lead to tough, difficult conversations because their motivation remains doing what is best for specific children they know well in contexts nobody knows better.
It means respectfully challenging people who say things like “he can’t help that because of his autism,” or “we can’t expect her to pay attention because of her ADHD.”
We need more of this.
We must point out the risks of assumptions and generalisations – that assumptions and attitudes can become self-perpetuating and lock a child into a pattern of thought and behaviour that holds them back rather than lifting them up.
These conversations about benefits and risks could – if we approach them honestly and in good faith –help us learn the things we must learn – leading ultimately to wiser decisions and better experiences and outcomes for our most vulnerable children.
In all of this we must not lose sight of the purpose of education – why we bother sending children to school at all.
Schools are places of academic study. Place in which children learn important, beautiful things so they know more and as a result can do more, so they can go on to live fuller, wilder and more meaningful lives.
This means accepting a responsibility to change – even transform – children.
To take them as they are, of course, but then help them become more by changing and developing
A responsibility to meet children where they are, yes, but also to go further and help them overcome their challenges. To do things they never thought they could do. To gift them opportunities to be more, to do more, than they ever thought possible, whether this is becoming the first woman to visit Mars or whether it is learning to eat all by themselves with a knife and fork.
To not be content with limited, confined lives because we believe some people incapable of overcoming their challenges.
To never be satisfied with “well that’s good enough for them, because..”, or “we can’t expect more given these circumstances.”
A child’s dyslexia means we must do better at teaching them to read.
A child’s ADHD means we must do better at helping them pay attention.
This does not mean being unrealistic and naïve by suggesting everyone can reach the same meritocratically measured heights if they try hard enough.
This is not true, and it is insulting to the dignity of those – like my daughter – who are very unlikely to become millionaires or famous musicians or artists.
But that’s OK because the true purpose of education is not to compare us against each other and in this we can all find dignity.
It isn’t about being the best.
This is hollow hubris and empty arrogance.
No.
It’s about learning more.
Doing more.
Becoming more.
In believing in the inherent value of us all as we are, but also in the capacity for us all to change, to overcome our problems and to astonish ourselves in achievements we once thought beyond our grasp.
Conversations about special educational needs are already tough and I predict they are about to get even more difficult.
Two opposing paradigms are on a collision course.
The first holds that developments in neuroscience are revealing powerful new insights about the way in which different human brains work, and as a result we are learning why some children in schools struggle and are rapidly developing helpful treatments and interventions.
As a result, many children now have the opportunity to thrive where once they were doomed to drown.
To those that take this position withholding diagnosis or treatment is ethically inexcusable.
The other paradigm rejects the claim anything new about human brain function has been discovered at all.
Those of this position believe there is no valid evidence there are biological causes for common difficulties such as ADHD and huge numbers of children are being inappropriately medicalised for quite normal human behaviours.
These people are worried about treatments and interventions that happen because of diagnosis because they think they come from a false premise, which makes them more likely to do harm than good.
The positions aren’t inevitably opposed – it is of course possible to believe some conditions are evidence based whereas others aren’t – but fighting over which is which doesn’t feel a helpful way forward either.
What would be better?
I propose adopting one simple principle; every action has potential positive effects and risks.
I then propose that before anyone does anything we involve a wide range of people in deliberately and carefully thinking these through.
For example, a dyslexia diagnosis might lead to improved self-esteem and access to helpful assistive technologies, but it might also lead to a sense of fatalism about reading that could conceivably limit progress.
ADHD medication may have the potential to improve academic focus leading to better results in tests, but it might also lead to dependency and progressively increasing doses to maintain the same effects.
Applying the principle properly would require us to look at individuals and contexts too, because these would have a bearing on the extent of potential positive effects and risks – this might require us to go beyond just education and into health too, which feels appropriate given the overlap we often experience in schools.
For example, perhaps people may be slower to recommend ADHD medications for a child with a family history of either addiction or heart disease than they would for a child in a family without this.
Many decisions about diagnosis and treatment will rightfully remain in the hands of families rather than schools and here the role of teachers and leaders would be ensuring that these decisions are fully informed – that families have considered both potential positives and risks before deciding what they should do.
This could look like this:
“Yes, we could put in for exam concessions for Sophia based on this diagnosis, and some children say they have found this useful, but before we go for that as an option, I want you to be aware this would mean all her exams when it comes to the GCSEs would be longer, which means she would be in exams a lot more of the time. Could you have a chat with her about this is something you all still want to do?”
Or:
“We could give Tom pink resources as this optometrist has suggested, but before we look at that I want you to read this summary of studies which shows there is no evidence this helps beyond the placebo effect. I also want you to be aware we have seen children who report finding reading harder on white resources after they were provided with coloured paper than before.”
I could go on, but I hope I’ve made my point – by exploring advantages and trade-offs over specifics we can have much better discussions than by getting into stand-offs over generalised and more abstract concepts.
As I write this I’m toying with the idea of a toolkit that holds all this in one place – a factsheet really – “here are the potential benefits of X.. here are the risks.”
Doing this right means being scrupulously professionally honest whatever paradigm you most fit into and adopting scout not soldier mode; claiming huge numbers children are being made mentally ill by normal school rules and routines would be as irresponsible as claiming a Ritalin prescription is an inevitable fast-track to illegal Class A drug addiction.
I hope by doing this we would evolve better more evidence informed conversations – and if we are to make any progress at all this is essential, because at present our systemic shared knowledge about special educational needs is dire. Too few people know the differences between how different diagnoses are arrived at, or the evidence bases behind widespread intervention practice. Too few people understand why the structure of different studies matters so much or even why debate is so charged and angry.
This might feel damning, but I don’t think it is controversial among teachers and school leaders who regularly say the aspect of their jobs they are least confident about are those to do with educating those with special educational needs and disabilities.
We must do better than this and this means learning more.
Conversations about benefits and risks could – if we approach them honestly and in good faith – help us do this, leading ultimately to wiser decisions and better experiences and outcomes for our most vulnerable children.
A few years ago, in the Golden Era of Edu-Twitter, Berny Andrews and I suggested the Department of Education needed a team of philosophers.
We were only half joking.
Very often the success or failure of educational strategy and policy is not in technical formulation or implementation but in purpose, and purpose is always about belief and philosophy.
I’m thinking about our crack team of edu-philosophers because I’m thinking about the possibility ECHPs might be removed as part of a drive to make our system more effective and more inclusive.
I understand why this might seem a good thing to do.
They are inconsistent and badly written, and most worryingly of all, the recent SchoolsWeek investigation revealed how immune they appear to have been to the evidence-informed movement that has led to improvements in many other areas.
Those that input into EHCPs appear to have little or no meaningful professional or personal accountability for their success or failure, which is hugely concerning given the legal powers they enjoy – if an ECHP says a school must do something then it must, regardless of whether that thing is useful or absolute rubbish, with the school alone held to account for its success or failure.
As something of an aside it’s interesting to note how this can place the law at odds with the SEND Code of Practice, which obligates us to remove barriers to learning.
The result of all this has been disastrous. Every year we spend more money on these plans while outcomes and experiences seem to get worse and worse.
Doing so – in theory – would lead to schools having more money and more say in how its spent and given how bad things are, the bar for better certainly feels quite low.
It’s also in line with my belief the best people to make decisions are almost always those closest to the problem.
Personally, I’d much rather my daughter’s SENCO and teacher decided what would best help her than a professional who might make their recommendations on an assessment lasting a couple of hours or less.
But – as things stand – I think removing EHCPs could be disastrous for our most vulnerable young people.
It surprises me a bit to find myself writing this, but even after some quite hard thinking, I’m confident we are too far away from a position where the benefits of making such a radical move would outweigh the risks.
Removing ECHPs and the associated individually ring-fenced funding would remove a layer of protection some children need in the hope improvements driven by generally more efficient spending would mean they wouldn’t need them anymore.
This feels very uncertain, firstly because I have significant doubts the wider system has the capacity and capability to improve its general inclusivity were it given more money to do so, because so much of SEND support intervention is formed from the same dubious evidence base the problematic strategies and practices in ECHPS come from too.
Getting rid of EHCPs won’t solve the bad practice problem. It will just result in the money being wasted by different people.
Secondly and even more worryingly, in a context of slashed budgets, unfunded pay-rises, expectation of further “efficiencies” and looming cuts I am not confident money saved by reducing or eliminating EHCPs would be spent on the most vulnerable learners were it detached from individual children. It doesn’t feel unreasonable to be concerned a primary driver of this might – even if this wasn’t the initial intent – turn out to be the desire to reduce overall education costs.
Given how under pressure we all are to reduce costs it feels deeply unlikely the billions saved would all go back into schools.
But plausibly, schools might see some of it.
If this were to happen I think it is possible provision for many and perhaps most children would improve, but this brings me back to the philosophy I began with – I worry that this utilitarian improvement would come with what J S Mill called “The Tyranny of the Majority” – really terrible experiences and outcomes for the very most vulnerable children who would find themselves stripped of their only protection.
A few years ago, I read a story about a woman who – after a terrible and disfiguring accident – was being considered for the world’s first facial transplant. The issue was that to make this viable what remined of her own face would have to be completely removed first. This would be worth it if the transplant was certain to work but it wasn’t and if it failed then she would be left with no face at all – an almost unimaginably horrifying prospect.
I see a similar risk in the removal of ECHPs in the hope that what will replace them will be better – perhaps it will – but what happens if it isn’t? What happens to our very most vulnerable children if schools don’t become inclusive enough to accommodate them if they don’t have personally linked funding?
I really worry this sort of thing might directly affect my family.
I worry in a few years we may find our choices for my daughter are reduced to mainstream with no extra help, or a Special School, when what we might want is for her to attend a mainstream school with a level of extra help that can only be provided with money allocated directly to her.
I hope my worries are unfounded.
Perhaps a plan will emerge that offers people like B better protection and support in a different way to the deeply flawed ECHP system.
But perhaps not and I think the risks of this must be very, very clearly understood and mitigated against if families like mine are going to have confidence things will get better as a result of change. We will need to be reassured this will not turn into a cost-cutting exercise that benefits other children at the expense of our own – that our own kids won’t become the minority to Mill’s tyrannical majority.
Personally, I’d far prefer we began by cleaning up what’s in ECHPs and holding those who input into them to account before we seriously consider getting rid of them entirely.
Sadly, one thing families like ours understand well is that no matter how bad things seem, they can always get worse.
In 1429 a French peasant with no military experience led an army against the Anglo-Burgundians, driving them from their bastion and forcing them to retreat across the Loire River.
At the age of thirteen she began hearing voices sent by God. They gave her a sacred mission to save France by expelling its enemies and installing its rightful king.
She was later captured and burnt at the stake.
This young woman is popularly known as Joan of Arc.
It’s a strange story, but perhaps not as strange to her contemporaries as it is to us – the medieval world was far more comfortable with miracles, visions, voice and direct divine intervention than we are today.
Our post enlightenment unease about the mystic and strange makes us seek explanation that makes sense in our very different paradigm, and a very common question asked about Joan today is whether she might have been schizophrenic – it’s the sort of question I’d expect from a curious, lively-minded Year 8 learning about her for the first time in a history lesson.
Oh dear.
What happens next might go something like this.
“3-2-1 all eyes on me and pens down – listen carefully. Historians generally don’t like to ask questions like this because all diseases and afflictions are socially constructed by us. The term schizophrenia was first used by a Swiss psychiatrist named Eugen Bieuler to describe a collection of symptoms he observed in some of his patients, including hallucinations, delusions and muddled thoughts. The term was first used in 1908, nearly five hundred years after the life of Joan of Arc. Bieuler did not know what caused it and even today we don’t have one test for it. We still don’t really know what it is. Asking whether Joan of Arc was schizophrenic doesn’t’ make sense because schizophrenia did not exist when she did. Her explanation of visions from God is valid and useful in the world she lived in where people believed this sort of thing happened quite often.”
Pity my Year 8, right!
I suspect my answer might make them and their classmates wish the question had never been asked, because there isn’t the sort of straight, easy answer young people like but, because I think it both interesting and important, I subject them to it anyway.
This – to a greater or lesser extent – is true of almost all diseases and illnesses.
Having modern terms for them doesn’t mean we have found some sort of empirical truth – indeed post modernists would have us believe there is no such thing at all – they’d say all truth is constructed by us.
Does this mean that we should embrace as sort of nihilism and abandon the pretence entirely?
Should we stop using terms like schizophrenia because they’re socially constructed?
No.
This would be big mistake because doing so would mean us denying all truths created by humans.
There are a great, great many of these and we need them.
Language philosopher J L Austin explored this in a series of lectures he gave in 1955, in which he coined the term “Performative Utterances.”
Austin defined these as words or phrases that just don’t merely describe reality but change it.
His best know example might be the words in a marriage ceremony. When a vicar says, “I pronounce you man and wife”, he or she is not just describing something that empirically already exists but changing reality itself.
Where a moment before there were two legally single people, there is now a married couple.
Whether or not you agree with the concept of marriage there is no doubt – within the context of our society – it is real. It is a reality we rely on and has very powerful social and legal ramifications.
We need it.
Whether or not there is an empirically “true”, perhaps even divinely defined concept called marriage is irrelevant because it is real in this almost entirely socially constructed world.
But this does not make it a free for all.
Validity and authority are – as J L Austin points out – integral to the validity and usefulness of socially constructed concepts. Children role-playing a marriage ceremony on a playdate don’t run the risk of transforming reality and becoming married by accident, because anyone performing a marriage ceremony must be given legal authority to do it and to get this, they must pass through well understood and agreed processes themselves.
For something to be real and therefore useful the legitimacy of the processes of construction must be understood and accepted.
This is why marriage is a useful term.
Schizophrenia is also a useful term because the diagnosis is arrived at by a well-understood framework of methods consistent between medical practitioners and it allows access to powerful and effective treatments that can demonstrably improve the lives of those who suffer from the condition.
What then of the terms we use in education?
Are these useful?
Many are, if they are used correctly and as intended.
For example, the term Pupil Premium is useful because it is a mechanism by which extra funding and support are directed to schools serving populations of greater social disadvantage. The processes used to assign a child with pupil premium status are shared and well understood which means we can use it as a good rule of thumb measure of provision and performance gaps.
Pupil Premium – like marriage and schizophrenia – is a useful term when it is understood and used appropriately.
Other terms are messier.
Let’s begin with dyslexia.
The NHS defines dyslexia as a common learning difficulty affecting up to one in ten people, causing problems with reading, writing and spelling. Its symptoms – again this comes from the NHS – include reading and writing slowly, mixing up the order of letters in words, being confused by letters that look similar and writing similar looking letters such as b and d the wrong way round.
The causes of dyslexia are controversial and its interesting to note how careful the language used by the NHS is – its website says, “it is thought certain genes inherited from your parents may act together in a way that affects how some parts of the brain develop”, a sentence which while superficially clear is full of cautionary qualifiers.
This uncertainty has led some researchers to argue dyslexia does not exist as a medical condition and instead is related to the great complexity of the English phonic code which makes it especially hard to learn compared to most other languages.
There is broad and helpful consensus that difficulties experienced by those with dyslexia are identical to those experienced by almost all emerging readers, which is why the strategies recommended by the NHS are the same – the most important being the expert, targeted teaching of phonics along with lots of shared reading and overlearning.
So, does dyslexia exist?
It’s irrelevant.
Who cares?
Whether there is a medical condition called dyslexia or not, the term is useful and without it many people would be worse off.
In this world those struggling to read without an explanation as to why are understandably fearful of being labelled as stupid given how mainstream scorn and ridicule of those who find learning hard is – think how accepted terms like retard, moron, cretin and idiot are compared to slurs attacking gender and race.
People with dyslexia talk about this a lot, about how relieved they were when they learned the reason they found reading so hard when others they knew found it so easy was not their fault.
The term dyslexia is useful, firstly because it is protective and secondly because it opens up avenues of good support. Those diagnosed with dyslexia can be given more expert targeted phonics instruction, more paired and small-group intervention and, with patience and hard work, will improve their reading.
Stripping them of their dyslexia identifier might well make these interventions less likely to succeed because it could lead to them internalising the idea they are “stupid”, affecting their confidence and making it less likely they would commit to programmes and interventions we have good evidence are helpful.
So, despite the complexity and controversy, dyslexia is a useful term and because it is we should continue using it.
While I know this might frustrate people, I have no interest in debating the medical status of dyslexia because to me it is unimportant.
But the utility of terms for many other educational difficulties are much more questionable because they are less well defined and because the interventions and strategies used to address them are not helpful and can – mainly through opportunity cost – even do harm.
Let’s explore some of these, beginning with a condition called Meares-Irlen Syndrome or sometimes Visual Stress, commonly diagnosed in children who find reading difficult to learn.
“Visual stress (pattern-related visual stress, sometimes incorrectly called ‘Meares-Irlen Syndrome’ or ‘Scotopic Sensitivity Syndrome’) is the experience of unpleasant visual symptoms when reading, especially for prolonged periods. Symptoms include illusions of shape, movement and colour in the text, distortions of the print, loss of print clarity, and general visual irritation. Visual stress can also cause sore eyes, headaches, frequent loss of place when reading and impaired comprehension. Visual stress is thought to be caused by the striped effect of black writing on white paper which causes over stimulation and excitation of the visual cortex.”
The factsheet goes on to say these symptoms are likely to be alleviated by tinted lenses in glasses or through coloured overlays, and that earlier controversy around these was resolved by scientific studies conducted by Professor Arnold Wilkins of the University of Essex in the 1990s.
The sheet links to a website of unclear provenance, which says about 5% of children may read up to 25% faster with a coloured overlay than without one, with no clear link to the study’s methodology, which I’d especially like to see given the suspiciously round figures.
The claim controversy around the condition and the coloured paper and lenses commonly used to treat it has been resolved is not reflected in more recent literature.
The most up-to-date review I could find, published in 2016 in the US National Library of Medicine concludes “the use of coloured lenses or overlays to ameliorate reading difficulties cannot be endorsed and that any benefits reported by individuals in clinical settings are likely to be the result of placebo, practice or Hawthorne effects.”
Further investigation bears this out – the consensus beyond those professionally or financially invested in advocating for the existence of such conditions is that there is no evidence for Visual Stress, Meares-Irlen Syndrome or that tinted lenses, or coloured paper makes reading easier.
The brazen doublethink can be astonishing.
Dyslexia UK – a company offering paid for private assessments for dyslexia even says “A number of research studies have investigated Visual Stress and have concluded that there is a lack of evidence that Visual Stress exists. They have also not found proof that treatments, such as Irlen lenses, are effective in helping people with reading difficulties”, but then goes on to advise assessment for the condition by a qualified optometrist anyway.
Here the validity of diagnostic processes is important because the associated outcomes are not useful to those subjected to them – they move emphasis from what we have good evidence for – like phonics instruction, to strategies like coloured lenses and papers we have no evidence for and are likely to make it harder for those having trouble reading to access helpful provision.
They may even construct difficulties and even disabilities in those who do not have them.
I have taught many children maintaining they are unable to read black text on white backgrounds. This is a very significant concern given that once they leave school, they enter a world in which they are unlikely to be given all the information they require on the coloured paper they have been taught to believe they need.
So, are there such things as Meares-Irlen Syndrome or Visual Stress?
The answer is almost certainly no, and this is important not because being empirically right or wrong is important but because such a diagnosis is likely to lead to worse provision and outcomes and so isn’t useful.
A child with this identifier is less likely to get support in reading we do know works because of the almost certainly incorrect belief that the coloured resources will do the job.
Sadly, education is full of similarly problematic pseudo-scientific diagnostic procedures and associated labels and if anything, they are increasing.
A big driver of this is the lack of substantive standardisation around many commonly used terms which are often used as descriptive catch-alls for things we have no real understanding of.
For example, while severe, mild and moderate learning difficulty are common identifiers on school SEND registers, there is no agreed process by which such labels are assigned to children, making any meaningful conversation about how to best help children assigned them impossible at systemic scale.
It is worrying how hard it is to get examples of how such determinations are made beyond a general sense they are for children who do not do well on tests, which could be for any number or combination of reasons including poor teaching itself.
This problem is surprisingly poorly understood.
Many commentators and even experienced school and systemic leaders seem unaware SEND registers are not products of well-understood and shared processes leading to robust, useful definitions but the subjective opinions of a vast range of individuals with little shared knowledge – for example a group of school governors I talked with recently were genuinely shocked to hear that a high number of pupils on a schools SEND register labelled as having learning difficulties was not in itself a useful explanation for a school’s poor performance in national examinations.
It might be assumed greater involvement and input of professionals such optometrists, educational psychologists and SEND specialists would provide more clarity but, unfortunately, these often create even more confusion. Many do not have standardised procedures either and the diagnostic terms they arrive at are often just as disputed as those used by teachers and schools.
There is significant debate and controversy around increasingly commonly used sciency sounding terms such as sensory processing difficulty, slow processing, trauma and attachment disorder, among lots of other labels found on documents such as pupil passports and EHCPs.
Sometimes there is debate about the existence of such conditions at all, and even when there is broad agreement about existence, there is disagreement about the specifics, making the terms of no practical use because the people using them don’t share an understanding of what they mean.
This is something else not systemically well understood by parents, school leaders, teachers or – too often – even those working within SEND departments in school.
The underpinning paradigm is that the diagnostic processes and the associated identifications are as sound and useful as medical diagnoses are, with robust and powerful interventions or treatments available to those assigned the labels. Philosophically this may well be because we have a medical model of educational deficit and disability that locates issues in learning within those who find it more difficult rather than the provision they receive.
This would not be so bad if those using these terms did not imply they were akin to medical diagnosis and did not mislead with statistics aping this different discipline. There was a good example of this in a recent training session I attended online on trauma, in which the presenter said, “bottling up stress and emotions increases risk of cancer by 50%.”
This – of course – is utter nonsense and isn’t even something that could be studied.
At best this is an unethical interpretation of a study that exists and at worst it’s just made up.
There is even evidence of this problem in the job title of the person in each school leading on special educational needs and disabilities – the SENDCO.
The “Co” bit is for “co-ordinator”, which implies the job is more enacting the advice of others rather than making decisions themselves about what might best help struggling children do better in the school context.
The underpinning principle is the idea children who find learning harder do so because they are fundamentally different to other children and that meeting their needs means finding out what’s “wrong” and then doing additional and/or different things to fix them.
As I began with, whether this was empirically true or not wouldn’t matter if the help children got because of the labels assigned to them benefited them, but – while it does for some, for example as it may do for blind and deaf children – it often doesn’t.
Instead, a determination or identification can easily lead to worse provision.
First, there is inevitable genericism when schools feel they are expected to enact lots of different strategies developed by lots of different professionals in contexts they have little experience in. The result is the construction of the “SEND learner”, who despite not existing has – nonetheless – great importance to the way schools attempt to meet the needs of those struggling to make progress in school.
Who then is this SEND learner? Not the highly academi blind boy in 9A, and not the wheelchair using girl in 8B either.
No, not these children.
Instead, the child is more likely to be boy, more likely to be Pupil Premium, more likely to behave badly, more likely to be summer born and – of course – much more likely to do badly on exam and tests.
What help do these children get because of identification? Do they get the best teachers timetabled to their classes? Do they get whole school policy formed in their best interests? Are the research bases for the interventions and additional and different strategies imposed on them rigorously interrogated, tested and assessed for impact?
Sadly, the answer to this is often no, and this is why commercial programmes like “Squiggle While You Wiggle” and “Write Dance” appear on the EHCPs of children like my daughter who finds writing hard, when what she needs is more supervised, encouraging practise to strengthen the muscles in her hands.
Thank goodness she goes to a school who know this.
Before going further, it is important and fair to acknowledge some commonly deployed techniques, programmes and strategies that are of no or little benefit to the children subjected to them may have value if applied properly, but this is often very tough to do and so is understandably rare.
An illuminating example of this can be seen in “movement breaks”, which seem to be appearing increasingly frequently in SEND support and EHCPs. Conclusions on the efficacy of these are predictably hard to find because – again predictably – there is no shared understanding of what a movement break is.
Is it having PE, drama and music on the timetable?
Is it walking between lessons?
Is it a twenty-minute break in the morning and a forty-minute lunch?
These are embedded features of the way most schools organise themselves which means if we use the loosest definition there is no obligation to change anything at all.
If the definition is tightened to mean movement breaks within lessons things get messier.
Would doing something like this be useful for children who find learning harder? Perhaps – but the evidence isn’t conclusive and incorporating such practice into a school would require a lot of work and feels like it would have a high potential for failure.
I’m not aware of any English schools even trying – if any are they’re very rare.
Instead, much more common are schools allowing some individual children to get up and move round the classroom or perhaps use an exit pass to go outside for an agreed period to wander about.
There is no evidence this does any good whatsoever – I’d be surprised if anybody had even thought it worth researching because the negatives are so obvious.
Allowing it has at worst the potential for disruption and disorder and at the very best significant opportunity cost, because if a child isn’t in a lesson doing what their teacher is telling them to do, they can’t learn anything.
The evidence base for some other commonly recommended strategies and techniques is even weaker.
Fidget Toys are a good example.
These emerged as a craze five or so years ago, have not gone away and are often still included in SEND support and even in EHCPs for children who have trouble paying attention.
The point of all this is the leap between identifying a child as having a SEND need and helping them is a yawning chasm – we cannot assume identification does any good and must be open to the plausibility it might do harm.
We must consider the very real plausibility that identifying a child with a SEND need makes their education not better, but worse.
We must also be open to the possibility this may be part of the reason that while SEND spending continues to increase, we are not seeing better outcomes or experiences for the children and families in the system. If identifications and associated interventions aren’t useful then spending more on them will just waste money.
Of course, schools need more money but without reform in the way it is spent more funding will not have a proportionate impact.
And we need it to.
Recently, my wife and I have been advised to pursue an ADHD diagnosis for our daughter who has Williams Syndrome and certainly does finds paying and sustaining attention much more difficult than most of her friends.
I suspect those doing the advising – outside of her school who understand perfectly – are bemused by our reluctance, but perhaps this talk has allowed you to understand why we might choose not to.
Would it help her?
Would it lead to more robust teaching, more careful prioritisation of curriculum and interventions that help her concentrate for longer? Or would it lead to badly conceptualised movement breaks and fidget spinners to occupy her, so she doesn’t bother others or get in their way?
Would it lead to pressure for us to put her on a potentially lifelong path of medication which is something as parents we absolutely do not want. Even if such a diagnosis were to help her in the short term how sure can we be that in the years ahead it won’t lower expectations and become an excuse for why she can’t do the things others can?
Does it even matter what we do?
Do we even have the power to stop this happening, or will she be labelled informally by her teachers and others who work with her whatever we do? If it’s inevitable, do we go for the diagnosis as the lesser of two evils so we can try and exert more control?
So many questions. So much we don’t know. So much trepidation and fear about what the future holds for our lively, inquisitive, curious eight-year-old girl and what the world will make of her – what people like you will make of her and who she is.
Do the schools you lead think about this sort of stuff as much as we do? Does it keep you up at night? While we don’t need you to lose sleep, we’d like you to think about the same things we do about Bessie for the children and families you are responsible for – the children with the least amount of time to waste, requiring expert instruction more than anyone else.
It’d really help us out if you did.
Part 2: Beyond Labels.
I began by explaining why asking whether a condition is real is going about things the wrong way, because what’s important is whether identifying anyone with anything is useful not whether it is real.
This is a good place to start thinking about solutions too.
Children who believe they need – for example – coloured paper to read are not usually lying.
It would be very unwise and perhaps even cruel for a school to announce that because there isn’t good evidence the coloured paper helps, its teachers will just stop providing it to the children who believe they need it.
This is unlikely to do any good and likely to do harm, because the removal of something the child and their family truly believes helps them will generate hurt, confusion and anger and this would make them less and not more likely to commit to strategies for which there is better evidence.
It would probably be more effective and kinder to continue providing the paper to those used to working this way while ensuring the child is also receiving more robust intervention. It would also be both kind and ethical to explain to these children and families that beyond Placebo and Hawthorne effects there isn’t good evidence such an approach is useful and the potential long-term consequences of such beliefs, so if they choose to continue, they are at least doing so from a more informed position.
People are absolutely entitled to believe anything they want to about themselves if they find the belief useful, and while schools can and should share knowledge with their communities, they should not attempt to persuade people they are not who they think they are. Many, many people find a diagnosis or identification hugely helpful because it helps them better understand themselves and gives them access to a community of shared experience where there is both emotional and practical support.
The sticking point is where the right of humans to be whoever they want to be runs up against the inherently collectively organised educational system which cannot be organised around what everyone wants without revolution.
I think there are plenty of people who believe the only way forward is revolution – those who believe that children learn in radically different ways to each other and that any system that doesn’t orientate itself towards highly personalised education for all is doomed to failure – as something of an aside this is why I think innovations in AI are so seductive.
These people think differences between children are under-identified and I can’t help wondering whether those giving advice – and there’s always so much advice – are even interested in helping improve the real-life ways in which schools and classrooms operate and how best to help struggling young people access them better.
At my most uncharitable I’ve even wondered whether a sort of moral purity is more important to them – a belief saying what they should think happen in their personal edutopia is fighting the good fight, leaving people like us to find concrete, realistic ways that improve the experience of vulnerable young people we professionally and often personally care about very much.
There is a powerful and persuasive lobby that’s been successful in convincing many young people and their families they are fundamentally and immutably different to others, and that without recognition of this they cannot succeed.
This is claim that – at best – is open to challenge.
But just telling the people who believe this they are wrong will not help and attempts to do so are driving much of the antagonism between families and schools.
It’s an unwise approach.
Moving forward requires us to steer clear of bunfights over whether things are real or not real, move beyond general identification and diagnosis and instead focus on the specific educational difficulties faced by individual children and deal with these whatever we or they believe about their origins.
Families, schools and other professionals all want children to succeed so instead of being drawn into fruitless and often hurtful arguments we should find ways to make children successful.
Before anything else schools must have – at least – a strong shared understanding of the ways in which they identify children with Special Educational Needs so that its possible to have meaningful conversations about the most effective ways to help them. All too often this is simply not the case with a lack of consistency within a school or MAT meaning there isn’t any shared meaning around the terms used.
When this is the case identifying labels become dangerous distractors.
Regardless of a diagnosis or label what’s almost always needed first is what’s often called quality teaching or universal provision. I’ve written about what I think this means elsewhere and in summary it means calm, consistent, dignified and predictable environments and clear instruction broken down into digestible chunks with responsive teaching – hard to accomplish but essential for all children and especially those who experience the most difficulty when trying to learn.
It also means reviewing curriculum with the interests of those who find learning hardest prioritised, because many of the issues experienced by these children originate in planning that thinks first of those who find learning easiest.
““They actually make sure there’s enough stuff in the curriculum for the fastest-learning students to be occupied all year. And so there’s far too much for most students. I think that’s logically consistent but immoral. When the curriculum’s too full, you have to make a professional decisions about what stuff you’re going to leave out, and the important point here is that not all content is equally important.”
This – of course – requires schools to be even more expert.
Schools that do these things well are likely to find the number of children requiring additional support will be far lower than those where the basics are not in place minimising issues caused by inconsistent labelling.
And all schools would benefit from honestly reviewing practice in their classrooms to ensure this vital first stage is in place -all too often this is just assumed.
In a classroom in which the basics are not in place the conditions and labels assigned to children is likely to be irrelevant – it’s not possible for additional-different provision to compensate for substandard general teaching.
Where adjustment, adaptation and intervention are necessary, these should be based on the specific educational challenges faced by children and not general terms for which there is little if any shared understanding.
We should stop talking about general characteristics of children who are Pupil Premium or have sensory processing disorders, dyslexia or ADHD or autism and instead focus on the specific challenges they face.
Schools are not hospitals or clinics and should not be in the business of identifying medical or pseudo-medical conditions.
That is not their job.
They don’t have the capacity to do it and where they are complicit in it, they should stop.
Instead, schools should be looking at the specific problems children have with learning and looking at specific solutions to those problems regardless of any identifier.
A dyslexic child’s problem is not dyslexia. It’s reading. Help them with that.
A child’s ADHD isn’t their problem. Concentrating might be. Help them with that.
What does it matter if a child’s distress around loud noises and big crowds is due to autism? Isn’t the problem the environment she finds upsetting? Fix that.
None of this is easy and we should not understate the scale of the challenge.
At an event last year, I was quite rightly scalded by Gary Aubrin for saying that much of the answers we need are “just” good teaching.
Gary’s point to me was there is no such thing. Teaching is hard to do well. Running good schools is hard too. There is a huge job of work for most of us just in this and until we’ve all got on top of this, nothing else matters.
Answers are hard to find, which is why we need those who lead teaching and learning in schools to be experts not just co-ordinators – they must have the knowledge and competence to know what best helps those who struggle.
And regrettably they must also be guards against those claiming expertise who either don’t have it at all or have it in contexts so different to schools their advice isn’t useful. This means not taking claims made by others at face value – it means having expertise to question and interpret studies, papers and the associated advice as I hope I’ve tried to do here.
It requires leadership not just co-ordination.
It requires leaders in school to know how identifications are arrived at and what the consequences are for those assigned these identifications. They must evaluate the impact of strategies and interventions, and they must be prepared to end them if they aren’t helping even when – especially when – they face pressure from others to continue with them even in the face of failure.
This is in support of and not in breach of the SEND code of practice, which legally requires us to remove barriers to learning, but it does means being courageous enough to stand up to well-meaning but damaging generalisations such as “he’s got a learning difficulty so he can’t do that”, or “his ADHD means he won’t be able to,” or “he’s not been diagnosed but you can just tell he’s on the spectrum”, whoever they come from.
We must not make claims that aren’t useful or acquiesce to those making such claims if these don’t lead to better provision.
Personally, I feel I understand the tensions quite well. Seven years ago, my daughter was diagnosed with Williams Syndrome, and this has taken me on quite a journey.
To begin with I wanted so much to believe she was different in exciting ways to others – that her genetic deletion and associated learning disability would be compensated for by special talents and an interesting, unique way of learning.
I was wrong.
She is – of course as all children are – unique and special but as we’ve discovered more about her, taking part in academic studies and working with experts in her condition, we’ve learned she has much in common with other children the same age.
She finds some things more difficult than most, but she doesn’t learn in a fundamentally different way.
Why did I not want to believe this when we first got her diagnosis?
I can’t be sure because memories are tricky, slippery things but I suspect it was because the idea of a learning disability felt shameful, and I wanted there to be compensations.
It’s hard to say that because it’s an admission there was something about my daughter, I was not able to accept. That I had the arrogance to want her to be something of my own making and not herself.
I’m ashamed of ever thinking it.
More important than my shame is if I had allowed myself to persist in this belief then perhaps, I’d have allowed her to be exposed to things that did not help her.
Perhaps she’d be squigging while she wiggles but wouldn’t be able to write as well.
Perhaps she wouldn’t be able to read because we wouldn’t have made phonics instruction such a priority for her school and us.
When I think of the joy she’s now experiencing reading road-signs and the names of songs she sees appearing on the display of the car stereo, of the little book she carries round to write her thoughts in, when I think of all this I’m struck breathless by the possibility she might not be able to do these things as well had I not been able to let go of my first, shameful framing.
Six years ago, my wife and I learned our then one-year-old daughter Bessie had been born with a rare genetic condition called Williams Syndrome – it’s fascinating and you should look it up.
It means with some very distinctive and charming personality features, Bessie lives with a life-long learning disability.
This is not something gone wrong.
It is not a problem.
It is who she is and we would have her no other way because were she changed she would not be her.
Seeing things this way changed my life, transforming the way I see my work.
Transforming the way I see my life.
In a way that feels very real to me it was a miracle that took me back to a journey when without really knowing, I had lost my way.
I was made to confront the fact education is not structurally set up in the best interests of those who find learning most difficult – those most likely to be identified with Special Educational Needs and those most likely to end up either informally or formally excluded from it.
In a context of worsening behaviour, rising suspensions and exclusions, and increased absenteeism and school refusal there is much debate around how schools can be more inclusive.
It is good we are talking about this, but it is also hard.
Today I’d like to talk about how schools with Christian values, and particularly Church of England schools might approach these challenges.
Before beginning it feels important to point out I do not believe these challenges are brand new ones – instead they are the result of an intensification of forces that have always existed in education.
I think schools have always often been hostile environments for children who find learning hard because they are expressions and mechanisms of a worldly meritocracy that values people for their supposedly individual achievements.
Society – underpinned by the meritocratic value system – honours the people who achieve most in obvious, familiar ways – those who make important scientific discoveries, produce beautiful art, build profitable companies, make big political decisions or – like you do – manage networks of many schools.
These people, people like you and me – life’s winners – are rewarded through prestige, large salaries and even national honours.
While only the most arrogant and least self-aware of these would claim their success down to only them, meritocratic framing requires us believe the successful deserve to be personally rewarded and we should view them as role models we can all learn from and perhaps – if we work hard enough – even emulate.
This is always something of a conceit.
Successful people are not successful because of their own rugged individualism.
Some were born into affluent families and benefited from an excellent education that propelled them into strategic entry level jobs obtained though good networks or even straight-up nepotism.
Others were lucky enough to be born with minds that learn easily and with good health, which meant they could focus their attention on their careers free of distraction.
I – of course – am an expression of the rule and no exception.
Here I am getting to feel all important by talking to lots of very important people in central London.
Is this because I am Very Clever and Worthy and Better Than Others?
No.
I had the good fortune to be born into a supportive and loving family and have – touch wood – so far enjoyed good health and a stable marriage.
I have the advantage of being financially secure enough to take risks with my work many others could not, which is why I am here now and able to do what I do.
I have had a lot of help and benefit from a support system that allows me time and space to pursue thoughts and interests others seem to want to hear about – for example, I wrote the first draft of this talk while my wife took our two children to the zoo.
About now she will be returning from the school run, which was bound to be even more stressful than usual because it is School Photo Day.
Could I be here if it was not for my advantages and privileges?
What would I have done this if I were a single parent?
Would I have the time?
Could I be here?
How many important voices are silent because those with them don’t have the advantages that allow them to be speak?
The point here is very few if any of us really “deserve” what happens to us, good or bad, but for society to give life meaning we tell stories of constructed correlations and patterns that downplay or leave out luck.
We like to think deserving people deserve their success and happiness because it is reassuring. It makes life make sense.
Believing people get what they deserve is comforting, providing a sense of order and security.
Schools are often this is microcosm – very often they most affirm and value those who find things easiest, and here the effects of meritocratic values are magnified, because perhaps the most important aim of most schools is that their pupils achieve good grades, constructing those who don’t for whatever reason as failures.
Even where individual leaders are uncomfortable with this – and many are – what they can do is limited because their own most important success metrics – things like SATs results and Attainment and Progress 8 – are oriented towards children achieving academic success.
Should we then abandon meritocracy as our underpinning value system?
Probably not.
None of the problems with it mean we should turn our backs on meritocracy altogether in the hope whatever we might dream up to replace it will be better.
I’m pretty sure despite meritocracy being mostly fiction, in the absence of a better framework we probably are better off with it than we would be with other underpinning structures that have been tried in the past.
Before meritocracy rose to dominance in the 1700s and 1800s, the value systems of many societies were unashamedly organised around inherited power and wealth with associated rigid hierarchies designed to keep everyone In Their Place.
A diverting historical illustration of this can be found in how remarkable it was Oliver Cromwell promoted some officers in his New Model Army based on their ability rather than their social position, an idea that at the time was considered rather subversive and even dangerous.
Hereditary status and privilege were no better than what we have now and would do great harm if we tried to reintroduce them, especially now the world is more secular than it was with religion less able to offer the traditional counter-narrative that regardless of rank all would be judged as equals by God after death.
Anyone curious about this might like to be look up the traditional medieval church painting of the Three Living and the Three dead, which was a stark and salutary reminder to those at the apex of the old feudal system about how little this would mean when their time came.
Tom Holland’s book Dominion is good on this too – about why Christianity was initially so repellent to the Roman Empire. Holland – who has recently been on his own journey back to faith – argues the Christian placing of all on spiritually equal footing threatened the very fabric of the predator society they had created.
But I digress.
The point is fictional or not, society is meritocratically constructed and in this world school leaders would be shirking important responsibilities if they stopped paying attention to academic success metrics because of philosophical objections.
Whether it is morally right, or morally wrong, better grades open more doors and give children more choice and control. Both practically and morally it isn’t wrong to focus on improving these, especially for those who have few other advantages.
This is why I have such a problem with famous successful people who have benefited from their formal traditional educations advocating wholesale root-and-branch revolution. It’s marked how often the people who do this come from great privilege and how rarely successful people coming from great disadvantage argue for an end to exam grades and qualifications.
In most contexts children benefit from a school paying close attention to their academic performance and schools that do not do this let children down.
We all know this.
But schools focused too much on only the academic performance of their pupils – those that lean too far into meritocratic values – leave space for the humiliation and degradation of many children.
We can talk as much as we like about how all GCSE grades are passes but the world constructs those who achieve lower than a 4 as failures because we’ve called a 4 a “pass” and a 5 a “strong pass.”
Similarly at primary children who don’t achieve the “expected” standard have by association not met systemic expectations and so have failed – at only eleven – to get to where the world says they should have got and are judged as less than classmates who have met or exceeded them.
This is antithetical to Christian values, to the values of those of other faiths and to many of those of no faith at all.
While Christians have evidence from the Bible for their beliefs in the inherent equality of all, most non-Christians will take no issue with the underpinning meaning of the following from the Bible.
Gensis 1:26 says that “God created man in his own image, in the image of God he created him; male and female he created them.”
Later the Book of Proverbs – Chapter 22 verse 2 says “Rich and poor have this in common: The Lord is the Maker of them all.”
This means that all humans – all children – are sacred, holy and of equal inherent value regardless of what they do or don’t achieve.
In his letter to the Galatians, Paul says, “There is neither Jew nor Greek, there is neither slave nor free, there is neither male nor female; for you are all one in Christ Jesus.” Paul doesn’t mean the differences between people aren’t real and aren’t important – instead, he is emphasising the inherent equality of all humans before God.
All are of value – each individual important personally to God. Each is loved, and the fulfilment of Christian values must mean valuing all.
While the world may say some people are of more value than others, Jesus certainly does not.
How can this tension – the tension between worldly meritocracy and what God says about people – be resolved by Christian schools?
How can they value each of their pupils – particularly those often identified with SEND who are most vulnerable to humiliation and exclusion – while existing within a paradigm that ascribes more value to those able to achieve most?
For some and for me once the answer is beguilingly simple – if we remove the barriers to learning that hold back those who struggle we can create a level field and create equality of opportunity. This – in my view – is the driver of a lot of “additional and different” practice, which relies on the assumption anyone is capable of anything,
But this doesn’t work because while we don’t like to confront it head on there are many children who for lots of different reasons find learning harder than others whatever we do.
Like the poor in Matthew 26:11, those who find learning harder will always be with us,
How do we help these children? How do we value them in a world that doesn’t?
This is a question the Church of England has already spent time wrestling with.
The Flourishing Schools document acknowledges the need to value all children and wisely concludes unless schools do this it is impossible for them to flourish.
It says:
“Flourishing can only happen when each and every child is treated with dignity. For they are all unique and inherent worth.. Therefore, they are to be loved unconditionally, enabled ambitiously, supported compassionately and championed relentlessly.”
How might this inspiring vision be realised?
Perhaps the answer is not in trying to resolve the tension between the meritocratic world and God, but instead in balancing them.
In Mark 12 the Pharisees set Jesus a trap by asking whether Jews should pay tax to Ceasar or not.
This appears to put Jesus in something of a bind. If He says they should pay taxes he places God below the Roman Emperor, but if He says they should not he is encouraging civil disobedience and places Himself and those following his direction at great risk for no benefit.
So, Jesus borrow a denarius coin and asks whose head is on it.
After getting a reply – Caesars – he responds by saying “Render to Ceasar the things that are Caesar’s, and to God the things that are God’s.”
This might offer schools a way forward.
Perhaps the instrumentalist outcomes of education – exam grades and associated success metrics – are equivalent of taxes to Ceasar – inevitabilities we cannot avoid and must pay close attention to whether we want to or not.
Like taxes, exam grades and the associated success metrics are here to stay, part of the world we all live in.
Whatever we do as schools they will always be there.
Individual children and young people who achieve top grades will always be celebrated by society through personal validation, more opportunities and more prestigious and often more comfortable lives.
Schools with pupils who achieve great exam results will always appear on the top of league tables, and those that don’t will be shamed, because this is Ceasar’s world, and his share will take care of itself.
So, what of God’s share?
What of the inherent value of all people -of all children?
What should schools do so those who find learning harder are as valued and meaningfully included as those who find it easy?
Here the Bible does not offer an easy outs or platitudes– it does not say those who begin with less are just automatically blessed and approved of by God. The Parable of the Talents in Matthew and Luke makes it clear as much is as expected from those who begin with little as is from those who are blessed with more. Here the servant who starts with the least but hides it away is the servant who is rebuked when the master returns.
Everyone is expected to contribute.
Our challenge is finding ways in which all can be included – ways in which all children in all schools can belong, share and contribute.
How, practically, can this be achieved?
The first and perhaps easiest step was one Tom Rees and I explored in our Five Principles Paper published last year.
The third of these principles was “success in all its forms.”
By this we meant schools should not only celebrate and affirm children for meritocratic instrumentalist achievements like exam grades and going on to prestigious universities, but also for other less measurable qualities like kindness, enthusiasm, commitment and service to others.
I think lots of school try to do this but too often their efforts end up as a sort of bless ‘em wooden spoons – consolations for those who can’t win in the zero-sum competition of the meritocratic real world.
This is not mainly the fault of schools.
As expressions of the society of which they are part emphasising the aspects of life that aren’t often instrumentally rewarded can seem naïve and unworldly, and it is sensible to worry this might lead to a general lowering of ambition and the inability to pay Ceasar his taxes.
As understandable as this is, it is still unfortunate because the results damage us all and might well be significant reason some of the most important roles in society are so low status and low paid; cleaners; carers; labourers; delivery drivers.
All these roles and many others are essential to us all, and it is troubling the lessons about them we learned during the pandemic have been so quickly forgotten.
Perhaps schools could do something meaningful about this by meaningfully recognising and celebrating the qualities of community and service.
Perhaps school reports should place just as much emphasis on how children contribute to their communities and their positive characteristics as they do on their test scores and grades.
Perhaps prize-giving ceremonies should centre these things too, honouring children for more than just academic, sporting or musical achievements.
Personally, I know how powerful this can be – my elder daughter Bessie has Williams Syndrome and an associated general learning disability and is near the bottom of the class in reading, writing and numeracy.
Despite this her school reports are a joy to read, because as well as being honest about where she is and what she needs to work on, they also include descriptions of a boundless enthusiasm that lifts all around her, what she is like as a friend and honours her for the many clubs and extra-curricular activities she takes part in.
Not very long ago her teacher emailed me on a Friday evening to tell me how Bessie had told the class that while she knew she wasn’t perfect, she was perfect for her family, and what an important lesson that had been for her classmates.
More of this for more children because it isn’t just children who find learning harder who deserve to be valued for more than what they achieve academically.
Indeed, it’s worth pointing out what a burden young people for whom learning is easy can find their own advantages if they feel this is all they are valued for.
Not very long ago I worked closely with a young woman who had spent years feeling crushed by the high data-driven targets that had been applied to her because she got high KS2 SAT sores. She said these meant nothing she did in school, nothing she learned or found interesting was really of value if she wasn’t going to finish with Grade 9s in everything.
This had depressed her, made her anxious, stunted her learning and wasted a lot of her time.
Only when released from the weight could she focus properly on her studies and find any joy in her work.
A focus on the other aspects of life is then, I believe, an important thing schools can do to be more inclusive to more children – to make it possible for more to feel belonging.
This is a good point to examine the risks and opportunities afforded by the recent changes announced by Ofsted, which will mean a “report card” of different indicators replacing an overall judgement.
This is a real opportunity because this really could lead to better incentives for schools to consider a wider range of ways in which children can flourish, but it is also a threat because less clarity might mean even greater focus on academic outcomes that will remain publicly available through examination results and associated league tables and judgements on attainment and progress that place a school on a scale from well below average to well above it.
We should not push for inspection or other accountability measures to lose interest in the academic work of those who find learning harder, because valuing these children for only their non-academic achievements is exclusionary and limiting too.
Doing this would further reinforce meritocracy because it assigns more potential and value to those who learn easily and have other qualities, constructing those who don’t find learning easy as being less complete.
Here it’s also useful to look at the oft-quoted John 10:10, which says that Jesus came so we all “may have life, and have it to the full.”
Life to the full does not mean us giving those who find academic work hard a pass out from it and just allowing them to do other things, because this would be to accept a limited life and would rob them of the wonderful gifts of academic work.
It isn’t just Christians who see this trap.
If we were to say that academic study isn’t important for some children, we would also be failing in our obligation to pass to children a cultural inheritance which is theirs by birthright, and we would almost certainly widen the existing divisions between those born with economic advantage and those born without.
Doing so is unchristian and anti-equity – something expressed well, albeit in some language we would not use today, by Robert Tressel in the Ragged Trousered Philanthropists when he wrote:
“Every little child that is born into the world, no matter whether he is clever or dull, whether he is physically perfect or lame, or blind; no matter how much he may excel or fall short of his fellows in other respects, in one thing at least he is their equal – he is one of the heirs of all the ages that have gone before.”
Christian or not, being truly inclusive must mean finding ways to include even those who struggle most in meaningful academic work.
For this I’d like our guide to be the Christian philosopher Simone Weil, who wrote a paper in 1951 called “The Right Use of School Studies with a View to a Love of God.”
Weil’s thesis is the purpose of school studies should be to increase capacity for prayer.
Without further explanation, I know this would be an extremely provocative curriculum intent for even the most confidently Christian school to adopt so please bear with me for a moment.
While Weil says “prayer,” the phrase “the state of prayer” fits just as well, and by this Weil means a state of perfect attention to something bigger than oneself.
Weil argues school studies – whether literature, mathematics, history, geography, science or whatever, are a good way of achieving this state when those studying them honestly and humbly submit themselves to their activities and exercises with the aim of learning to pay attention and not for external validation.
Weil goes as far as saying those who pursue their studies with the aim of achieving top grades for their own sake will not be able to study properly because this would distract them from innate wisdom found in their subjects.
She says:
“Students must work without any wish to gain good marks, to pass examinations, to win schools successes; without any reference to their natural abilities and tastes, applying themselves equally to all their tasks, with the idea that each one will help to form in them the habit of that attention which is the substance of prayer.”
This is very hard to do.
When learning something new most of us are constantly on the look-out for shortcuts that get us to an answer quickly without a full and complete understanding – we often feel wired to look for ways to cheat the test. I have a hunch this is why recent technological attempts to gamify learning don’t work as well as we’d like them to. For about three years I diligently subjected myself to fifteen minutes a day of DuoLingo German only to find at the end while I’d accrued thousands of points and risen up many of its league tables, I still wasn’t really that much better at German. The problem, I think, was I became so fixated on keeping my streaks and getting silly meaningless awards that I lost sight of what the point of it really was.
The prouder we are, the harder we find to prevent our egos intruding on what we study, especially if we are learning about something we already have feel strongly about.
As a religious person I am always aware of this when I read arguments written by atheists dismissing God – even when the argument is coherent and logically organised, I find myself internally interrupting, arguing and disagreeing even before I’ve finished reading – arrogantly inserting myself in the work and by so doing risking misunderstanding and mischaracterisation.
The problem here is caused by us seeing learning as the means to an often-selfish end – a weapon with which to win the meritocratic fight through high grades, or armour to protect ourselves from the perspectives and opinions of those we do not approve of or dislike.
Weil argues this is fundamentally wrong – even unchristian. Instead, she says, we should be seeking to truly understand and know, and that the harder and more challenging the study the better because this allows more opportunity to learn to be better at properly paying attention.
She says:
“It does not even matter much whether we succeed in finding the solution or understanding the proof, although it is important to try really hard to do so.”
For those of our children who find learning harder this is brilliant news because it gives them equal status to their friends who find it easier.
By making the aim to pay attention and to really learn and understand rather than being at the top of the class we make the endeavour of learning one all can take part in on an equal footing, which feels like an expression of true inclusion. This realisation has changed my teaching practice – for example I am now very clear about how much I disapprove of those in my classes competing over scores in tests because this is exclusionary to those who improve but don’t finish top. I am not naïve – I know they do this anyway when I’m not around but I think it important those who struggle most see their history teacher is on their side in this – that while those around them might think the point is the highest score I do not.
Valuing the work – the process – means that those who find learning hardest – those most often identified with SEND – have the opportunity to be just as blessed as those who find learning a breeze.
A teacher, school or even a MAT adopting Weil’s approach could not just tag this on – it’s a whole philosophy and would mean orientating recognition and honour towards humble, diligent effort and away from those who rise to the top because they just find it easy to fly there.
It might also mean changing the way schools try to improve academic standards – a shift away from systems designed to track and drive progress through numbers and grades and a refocusing on the substance of learning itself – assessment designed to identify what children know and adaptive planning that takes children from where they are to the next step on the ladder – an assessment-teaching cycle that aims not to boost grades but to make it easier for children to pay proper attention to what they are learning.
This might on the face of it seem daunting and even scary – many of those who run schools have become so accustomed to things like progress against target grades and numerical data input that a world without them seems unimaginable.
The good news for those considering a realignment is that much accepted practice to chase grades and drive progress is – bluntly – nonsense anyway.
For example, target grades at an individual level are invalid making common intervention cycles based on these meaningless.
Saying things like “aim for a 4”, or “get them to a 6” is usually just plain silly because grades are so abstract – children get the grades they do by learning more and doing more so a focus on the substance of learning might well result in better outcomes too, even for those who find learning easiest.
I heard a good practical example of this quite recently from a maths teacher at a highly selective school depressed by the number of Grade 9 Maths GCSE students he saw who struggled to transition to “A” Level.
The reason – he felt – was that many of these were clever enough to memorise formula and equations they did not really understand and while this was enough to get them the very highest grades at the lower qualification it made taking the step up extremely challenging because they had little understanding of the underpinning principles and structures the new content built upon.
Some – I suspect the humbler and wiser – were able to accept and realign, but those who had internalised the meritocratic idea the point was to finish top found it much harder.
As difficult as it might be to do, truly inclusive schools should not focus directly on grades.
Instead, they should focus on the process of learning because getting better at this is an appropriate ambition for everyone from a child with a learning disability to one who aspires to study at Oxford.
I think this is the most beautiful way to see inclusion I’ve come across.
It is now old-pat Growth Mindset freed of the unhelpful and dishonest rhetoric that led to people saying things like “if you work hard can become anything you like,” which further humiliated those for who this was not true.
People like my daughter.
A school built around Weil might instead say, “no, you won’t all be the best in the world at this but all of you can, by carefully and diligently completing the work we set for you, learn more and it’s in doing that work – in paying proper attention – that you win our respect and admiration.”
It’s comforting to me that perhaps – perhaps -such an inclusionary educational philosophy might place children like Bessie on at least a level playing field.
And the good news is so far, he school – A proudly Church of England primary with a Catholic Provision – has succeeded in this. Bessie continues to delight herself with what she learns.
She doesn’t find reading as easy as many others, but each day she gets a bit better, and she loves to pore over books.
She loves learning.
It delights her.
Just last week she came home unable to stop talking about Everest, Tenzing Norgay and Edmund Hilary and was delighted to be able to take in a prayer flag to show her friends that her mummy picked up on a work trip to Nepal where she was working on helping local communities find innovative solutions to their local problems.
Bess won’t achieve top grades when the examination cycle rolls round to her. She may never sit exams. We don’t know. Whether she does or not will depend on what is best for her.
Knowing this frees us from what ultimately is a distractor from what learning should be about anyway – it allows us to see the point is Everest, Norgay and Hilary not the grade she gets on a report she might one day write about it.
It allows us to see that what matters is whether what she learns helps her, enriches her, fills her with wonder, awe and optimism, equips her to flourish and thrive.
How strange it seems when we first learned about who she was we cried because we thought it was bad news.
Isn’t this what we want for all children?
What a gift she has given us – one her academically very able but more nervous younger sister is already benefiting from too because it has made her parents better parents.
Bessie has led me to a place where I understand her goals to be the right goals for all of us.
Not to aim for the highest marks but instead to try to learn to pay attention so it is possible to really learn – about mountaineers and dinosaurs, about Samuel Pepys cheese and most importantly of all, of how much God loves her the way she is.
Her school is exceptional, and I know what they do is not easy but could it be something we might aim for?
AI is stalking the world for problems it can present itself as the solution to – problems you did not even know you had.
It will organise our calendars and write emails to our bosses and employees.
AI will paint our pictures and script our film.
It will write our poetry and letters to our lovers.
For teachers it brings great news too.
AI can plan your lessons – saving you time and easing your workload.
Except it won’t, because it can’t, because planning is a human process that only happens in human minds.
Those that think AI can plan make an important category error because they don’t understand what planning really is and have confused it with creating resources, which AI is very good at.
Resources – PowerPoint slides, booklets, worksheets or a physical written plan are products of planning but aren’t planning.
Planning is a teacher thinking about the material and how best this can be taught to a particular real life flesh-and-blood class.
AI cannot do this.
AI enthusiasts and its early adopters are not the first to make this error – the confusion between resourcing and planning has been a problem for teaching for as long as I can remember, dating right back to when I was an NQT, and the scheme of work was kept in the department office in bulging box folders stuffed with worksheets and coloured OHTs. As inexperienced as I was then, to me, “planning” a lesson often meant little more than finding something for children to do related to the topic at hand.
Later the internet arrived, and the earliest manifestations of TES resources and other file sharing sites allowed teachers to find activities and resources designed and created by teachers far beyond the individual school they worked at. Also, around this time, the rise and rise of email and file-sharing mechanisms (“the shared drive”) promoted greater teacher-to-teacher interactivity and it became commonplace – even typical – to share out “planning.”
One history teacher might make the PowerPoints for Year 7 Normans while another would do Year 8 Industrial Revolution saving time for both.
This was never – as James Theobald has written very well about here – very satisfactory.
Tasks and activities that made intuitive sense to the person making the resource made far less sense to a different person because they lack nuance on how each slide should be introduced and framed, or the success criteria of the tasks.
Even an image is never just an image – a portrait of Elizabeth I, for example, can mean many different things depending on the angle at which it is approached, which differs according to a teacher’s plan.
The point is that the resources are not the plan – the plan is the underpinning thinking and without it experiences and associated outcomes are impoverished.
It is – of course – possible to turn someone else’s resources and plan into one of your own by thinking through it, adjusting and tweaking until the whole thing hangs together in a way that makes sense, but this – in my experience anyway – usually takes just as much time as planning from scratch and is far less satisfying.
AI is so problematic because it allows the products of planning – resources and timed sequencing – to be produced with minimal thought.
In seconds I could enter “Plan a lesson for a group of Year 8 pupils on the Reformation of the English Church”, but what would be spat back at me in even less time wouldn’t be a plan at all unless I sat down and thought it all through, a process which would almost certainly result in me doing something different anyway, because I’d then be thinking about my particular class and the children in it, what they had and hadn’t covered, who had missed bits and who was likely to need extra help.
This is something Martin Robinson got to a long time ago in this short but very beautiful blog post about how a Design and Technology teacher’s plan for teaching a Dovetail Joint existed in his mind as a product of decades of thought and experience and how shameful it was this was not understood.
There are many AI enthusiasts who argue AI should only ever be used as a starting point to generate ideas – but while this is where the journey begins it is not where it will end.
As planning appears to take less and less time and we privilege its artefacts over the thought that creates then, we will be expected to do other things instead and given how much teachers generally value planning we should be concerned about what we may be expected to do instead.
In the short-term AI may save us minutes and hours, but everything I have ever known in twenty-years working in education convinces me when something is taken away from us it is always replaced by something else.
When I first started teaching messages in pigeon-holes were soon replaced by email.
Do you have more time?
Then there was a paradigm shift on marking in secondary schools.
Do you have more time?
Then the data war and half termly data-drops and associated analysis became much less frequent and onerous.
Do you have more time?
What then if “planning” lessons by AI becomes normalised?
We all know teachers should have high expectations of pupils.
Teachers who think their pupils can learn and do lots set more challenging work than those doubting their capacities and this leads to more progress.
Nobody – quite rightly – argues against high expectations.
Officially you can’t even be a teacher if you don’t have them – they’re in the Teacher Standards.
But high expectations aren’t the same thing to everyone. Given the huge variability in our education system how could they be?
Different teachers and schools demand different levels of effort and have differing standards on acceptable general behaviour.
But we don’t talk about it well because being accused of having low expectations isn’t just an observation – in teaching it’s a personal and professional insult.
Describing someone as having “low expectations” is damning, meaning at heart we think the person is not a good practitioner.
Thinking about whether we have high enough expectations makes us angry and defensive.
But it shouldn’t – ideally there would be no reason to take it so personally because our expectations are more products of our environments and experiences than deeply held and immutable core beliefs.
If we have always been managed by terrible bullying bosses, then we will expect future bosses to be terrible and bullying. If we have always hated exercise, then we will expect a new sort of exercise to be horrible.
Conversely if we have always enjoyed Indian food, we’ll be excited a newly opened Keralan restaurant and if we’ve always liked science fiction films and loved Dune 1 then we’re more likely to rush to see Dune 2.
The point is expectations are not ethereal or objective – they are set by what we have seen and experienced before.
This is true of standards in schools.
If a teacher has only ever worked in schools in which behaviour is poor, they are far more likely to think this normal than a teacher who has only worked in schools where behaviour is excellent. If a leader has never worked in a place in which the completion of lots of outside school study is normalised they are far less likely to believe children capable of it and more likely to be satisfied with less and lower quality work.
This makes it hard for people to change their expectations – telling someone their expectations are too low doesn’t usually work because this is rhetoric against experience, which is a battle that only ever has one winner.
Our experiences are very powerful.
If you’ve worked in or led a school in which students angrily swear at staff regularly or where violence is not uncommon it can be very hard to believe much better is possible. When there are a lot of dysregulated children behaving chaotically the idea it’s possible for a school to be truly calm and orderly can seem absurd.
To these people – those struggling to stay afloat in the most challenging of circumstances – the idea other places have succeeded where they have apparently failed is often laughable and it’s logical to explain examples of success away; perhaps their demographic is radically different or perhaps they are faster to exclude the children who are most challenging. Perhaps they have more resources. Perhaps they just have more staff.
This is complicated because such explanations might be true.
But sometimes they are not.
Even in the areas of highest challenge children can behave as well and work as hard, but knowing this often means experiencing it.
Some schools are genuinely turning the dial, but for lots of reasons it can be hard to accept this.
This problem isn’t unique to teaching.
Prior to the Joseph Lister’s pioneering work on antiseptics the death of very large numbers of patients after surgical procedures from infection was regarded by doctors as sad but inevitable. When Lister began achieving astonishing survival rates it was natural some of the first reactions were of disbelief; firstly, the improvement seemed too good to be true, and secondly the idea tiny invisible “microbes” could kill a powerful fully grown man was logically absurd.
These sceptical reactions were not a demonstration of low expectations – they were a sensible and entirely reasonable reaction to something they had no reason to believe and would have been fools to take on face value, especially when the new methods slowed surgeons down.
The initially sceptical are not the villains. The villains of the story are those who refused to look at the evidence or to change their practice even after it became clear a huge breakthrough had been made.
Why didn’t they change? It’s impossible to be certain. Perhaps they had wrapped up their personal egos in their professional status which meant they felt any admission of prior mistakes reflected on them as people. Perhaps they were overcompetitive and couldn’t deal with the idea a rival had found something they missed.
Lister’s attitude was not helpful. Arrogant, contemptuous and dismissive he called his peers “murderers”, which led to further defensiveness and entrenchment.
There’s lots to learn from this.
It’d probably be better if we viewed our expectations as expressions of our past experiences rather than expressions of our moral characters. Given all the rhetoric this isn’t easy. Quite recently a friend of mine questioned whether my expectations were as high as his, which for a second made me bristle until I thought about it and realised his perspective was different because he had spent much more time working in schools achieving excellent outcomes than I had.
It wasn’t personal.
Not taking things as personally would make it all much easier to talk about – easier to admire others and learn from them – easier to understand and appreciate nuance and context.
Those achieving brilliant things shouldn’t get carried away either – they should remember their results are better not because they are better people but because they have had the privilege of a different perspective.
It isn’t easy to get to this point – accountability metrics in England are inherently competitive and create winners and losers with all the associated hurt and hubris.
But education isn’t a game and when we play it like it is the losers are the children we all want the best for.
It is hard to talk about things when people don’t have a shared understanding of the words they use, and words usually don’t mean anything on their own – terminology is only given meaning through practical examples.
Two people – for example – both thinking they work at “warm-strict” schools can find differences in how they interpret the phrase mean their disciplinary systems have very little in common.
Discussion of “inclusion” is affected by this ambiguity, because the people using it often mean very different things.
What is an inclusive classroom?
To get to a point where this can be a meaningful question, definitions and examples are needed to avoid misunderstanding and misinterpretation.
On its own the word “inclusion” means nothing.
To be included or excluded there must be something to be included in or excluded from.
Alone, inclusion is only a word in an unfinished sentence.
Schools have multiple functions, and this makes assessing how inclusive they are tricky; a school can be more inclusive in some aspects of its practice than it is in others.
A friend of mine who works for Children’s Services helped me understand this a couple of years back, after I expressed frustration about internal truancy at the school I was working at and how being in the building was pointless if children in it weren’t learning.
He pointed out things weren’t as simple – that many of the vulnerable children he worked with were more of a danger to themselves and others if they weren’t under adult supervision at school. He recognised these children probably weren’t learning much in the schools he placed them in, but for them the protective function of a school was more important.
His definition of inclusion was different to mine and so were his success indicators. This is a tension I’m not comfortable with but get and respect.
Inclusion in classrooms is easier to understand because the primary purpose of classrooms is learning.
To be inclusive the children in them must learn.
Creating and sustaining an inclusive classroom is difficult at the best of times.
Children often lack an inherent drive to learn what is on a school curriculum, and many would often prefer to be elsewhere.
Children who would rather be doing other things are not unusual or deficient. Nothing has gone wrong if they don’t want to do algebra or osmosis. It is normal for children to want to do stuff they want to do more than stuff they don’t. This means teachers often have reluctant audiences and must be skilled at directing their attention and motivating them.
If a history teacher fails to spot a child is drawing anime characters in their jotter instead of answering a question on the feudal system, they are not included. If a child daydreams away the day and nobody intervenes, they’ve not been included even if they have been present in every lesson. If a child can’t read the text a teacher gives them and then copies out the questions instead of answering them, they have not been included.
Before getting anywhere near SEND designation and the specific difficulties some children face in learning it’s important to understand issues around inclusion in classrooms affect all children – not just a few, and that the degree of inclusion and exclusion to learning children experience day-to-day and lesson-by-lesson varies and fluctuates.
Inclusion is a continuum, affects all children and changes over time.
The continuum is affected by the teacher, the behaviour of children, the curriculum and lots of other things too.
It’s possible for a classroom to be more inclusive on Monday than it is on Wednesday and for it to be less inclusive in the first half of the lesson than it is in the second. If there is a topic on the curriculum that lots of children are naturally interested in, then it may be easier to make the room more inclusive than if it is a topic that’s less compelling, and this may vary from child to child.
The learning vulnerabilities of children change over time too – something as simple as the normal fluctuations in a child’s mood can make it easier or harder for a teacher to include them in the lesson – techniques that worked fine one week may not work as well or even at all the next week.
Neither inclusion nor exclusion are fixed states, and so trying to become inclusive as if this were a threshold to cross is to set an impossible aim, because the conditions affecting it change all the time and however inclusive a classroom is there is always more that could be done.
Instead of trying to become “inclusive”, teachers should aim to be more inclusive more of the time and work on strategies and practices that make this more likely.
Seeing things this way means better professional conversations and better decision making, because it removes the moral coding the term has assumed, which leads to defensiveness and theatrical performativity for other adults.
It also means people can talk more honestly about where they really are without fear of a potentially humiliating judgement, and might allow them to look at small, specific things they can do to move on the continuum without feeling the journey is too long and hard for it to be worthwhile even beginning.
2.The way children learn is more similar than different.
There are people who believe children learn in very different ways and this means inclusive classrooms require different children doing different things.
This belief was at its peak when VAK learning styles were in vogue, and while these have been for the most part driven out of education the underpinning beliefs remain with us.
This is probably because the existence of a diversity of learning styles is a view now held by much of society, and the claim humans learn in very different ways is often repeated as fact even though there isn’t strong evidence it is true.
Such beliefs make it logical to believe some children can’t learn much in school if teachers do not match instruction to the different ways in which individual children learn.
It has even led some to argue schools are not capable of being inclusive because they are incompatible with the pluralistic ways in which children learn.
This view was (in)famously explained by the Ken Robinson’s “Changing Education Paradigms” video, which went further and argued the uniformity of schools destroys the innate creativity of children.
Those that believe this think teaching classes of children the same thing in the same way is inherently exclusive because being inclusive means different children doing different things.
Some may be working on coloured paper.
Some may be wearing headphones or using computers or tablets.
Some may be using fiddle toys while others sit on beanbags on the floor.
In classrooms like this the teacher will not be instructing the whole class – instead they use different methods with different pupils. Occasionally overstimulated children who need a break leave the room quietly to stand outside while the re-regulate before rejoining the class.
The room has a cheerful productive hum about it.
This is what teacher training twenty or so years ago held up as the ideal, and while this vision isn’t as often explicitly articulated it still has influence, particularly when inclusion is discussed.
SEND support built around conceptions of “additional/different” can imply inclusion must mean different things for different children and don’t sufficiently emphasise even when individualised strategies have value, they can’t be effective in contexts of disorder and confusion.
Another cause of confusion is how the assessment of individual needs of children is often done through processes detached from their context as members of classes.
Teachers aren’t private tutors, and don’t typically teach children one-on-one, which makes teaching strategies designed to work in this context of limited use to a typical mainstream teacher – what might be a helpful suggestion for an adult working with just one child can be terrible advice for a teacher teaching a class of twenty-nine.
When they try the result can be chaos.
Often it means confusion, unreasonable workloads and an inability to establish and set up the predictable and consistent routines and systems that allow lots of different people to be in one room working together.
This is not unique to teaching – any context in which there are lots of humans in one place – from battlefield armies to building sites to football grounds have common expectations, rules and modes of behaviour allowing individuals to work together towards a common aim, and this usually means doing many things in the same way.
It would be odd if classrooms in schools were the only exception to this; to be included children need agreed expectations of how to rub along together.
A reasonable response might be it isn’t the pluralistic teaching style vision itself that’s wrong, but that those who attempt to enact it aren’t doing it right – that teachers need to be better trained and resourced and if they were then more children would be included and it would be possible to create places in which lots of difference and adaptation become part of the culture.
The argument deserves to be taken seriously because any good idea can be ruined by poor resourcing and implementation. We must not be afraid of idealism because with pragmatism and good logistics this is the only thing that changes the world for the better.
In this case, however, it doesn’t fly because there isn’t enough good evidence children do learn in very different ways, which means solutions designed from this point beg the question by proceeding from a flawed premise.
Even if it were true there would be significant questions around scalability because we don’t have good examples of where such approaches have been successful, which means there aren’t good examples from which the system can learn. Finally, it’s worth noting that calls for the entire restructuring of the entire system and hugely increased funding to pay for it all aren’t serious – this would be a huge risk and secondly because without the resourcing to pay for it there is no path to effective implantation.
We should always be open to new and compelling evidence but in the meantime good intentions can’t excuse poor outcomes – visions of an ideal world can’t be a reason to do things we know won’t work in the world the children in our classrooms are taught in.
What then works better?
To understand we could look at the needs of children identified as having SEND, found on documents like pupil passports and Education Health Care Plans.
Here it is striking how typical strategies that are features of strong teaching for all children are emphasised; behaviour management techniques such as “have consistent, predictable routines”, and “responds well to praise”, and teaching strategies such as “break tasks down into smaller steps”, and “regularly check for understanding.”
Such strategies aren’t suggesting some children need radically different teaching to other children, but the problem is by identifying these as individual strategies for individual children there’s an implication these are things a teacher must do just for them rather than aspects of teaching practice that should be in place for everyone.
It is possible I’m overreaching, and I’m open to the possibility there may be some circumstances and conditions in which to be inclusive teaching must be extensively adapted but it is implausible most of the approximately 40% of children identified as having a SEND need at some point while at school have been assigned this label because they all learn differently to others.
And even where children have been identified with explicit and specific learning difficulties there is still little evidence this requires wholesale changes to instruction.
Where adaptations are most obvious it is often not clear these are of benefit.
For example it is common for children experiencing difficulties in learning to be prescribed different coloured paper or lenses, despite there being no conclusive evidence such practice outperforms the placebo effect. Worryingly, this is true of many separate specific strategies and interventions claiming to help vulnerable children, and evidence they do help is often limited to anecdotes on company websites and promotional leaflets.
This isn’t me nitpicking over minutia – it is important teachers know this because if there is no evidence something does what it claims to, then they shouldn’t expect any learning benefit from applying it. Conversely if someone insists something does work then a teacher should expect to see benefits. Whether something is likely to work or not is important for teachers to know because it will affect their planning and instruction.
There are few magic bullets.
The basic tenants of good teaching remain the same for just about everyone.
Where teaching is good it usually shares common principles. Even where it may appear to be quite different – for example someone teaching a person with a profound learning disability how to use cutlery, differences are usually superficial with the deeper structures – breaking things down into small steps and modelling – the same.
All this often means teachers often don’t need to target supposedly personalised strategies at only children specifically identified as needing such strategies – it’s easier, more logical and more beneficial for more children for the teacher to make sure these things are features of their regular teaching not add-ons for a select, special few.
Teachers seeking to make classrooms more inclusive should first focus on things that need to be in place for all children before attempting to make extensive individual level adaptation and differentiation. Those that do may find they are meeting the needs of many more children as a result.
When this is done well, inclusive classrooms do not look very different to good classrooms in general.
They are calm, quiet, orderly and clear.
Teachers explain things clearly in small steps and then tell children explicitly what to do. They pause to check kids have understood. They respond and adapt if they don’t. They have high expectations and maintain high standards, being predictable and consistent with routines, rules, rewards and sanctions so that more children are included in the group.
They speak to children with respect and ensure children treat them and their classmates with respect too.
Inclusive classrooms are places in which the teacher knows children in the room as individuals and targets the right question to the right pupil.
Inclusive classrooms are first good classrooms.
While this may not be sufficient, it is necessary, and no amount of bespoke, additional pedagogy can compensate for poor teaching.
Teachers must be careful attempt to meet individual need through individual adaptation don’t compromise the necessary base conditions so that nobody succeeds – it’s much harder to break things down into logical clear steps for everyone if a teacher is trying to do this for lots of different children in different ways because they think this is what is required of them.
So why do teachers feel they must do this, even when it’s against their better judgement?
Perhaps sometimes it happens because teachers lack confidence in their ability to create and maintain a calm and disruption free environment, or when leaders insist on seeing different things for lots of different children because they think this is what inclusion means. An example of this happening might be a SENDCo visiting lessons, observing only children identified as having SEND and then asking for more individual differentiation as a solution to a disorderly environment in which few children are able to learn, when the correct solution is at class and not individual level.
This does not mean all children find things equally easy.
Those doing so are acting ethically and logically – as things stand there is no mechanism for parents to improve the overall quality of their child’s teaching, so if they are struggling seeking more bespoke support is their only option.
That said it seems unlikely we are seeing more struggling children because the nature of children in general has changed very quickly over the last few years.
More likely is in a context of rising poverty, increased time spent by children online, recruitment and retention issues, the collapse in children’s mental health services and declining real terms funding it is now harder for schools to create calm and positive classrooms for all, resulting in more kids struggling and being identified as having a SEND need.
This might mean better diagnosis or even overdiagnosis, but it is just as likely it means there are children with greater need who may have coped or even thrived before but are now not able to because we are experiencing the result of multi-system degradation.
These are difficult problems because many are not within the control of individual teachers.
While it is possible for teachers to be more inclusive when they focus on it, their efforts will be more impactful when school leadership supports them by creating conducive conditions to try – as hard as it is – to mitigate the effects of wider systemic failures.
All children benefit from consistency and predictability and if the learning and behavioural norms at a school aren’t clearly communicated and understood then associated confusion and disorder makes it hard for teachers to include children in their lessons.
Again, I think of my own daughter here.
When I think of her going to secondary school in a few years’ time I worry most about potential lack of clarity around things like how to behave at social times and on the corridor between lessons – if this is left to her to work out she’s more likely to make poorer choices and become dysregulated, which would make it harder for her to focus on her learning and harder for her teachers to include her.
This – again -is an example of how attending to getting the basics right for all children benefits those most likely to be marginalised most.
Answers will not be found in throwing more life belts to our drowning sailors – instead we need a better ship.
But there are dangers to what I’ve said so far -the most serious is a misinterpretation if the basics of schools are improved there would be nobody left requiring personalised support, and this isn’t true.
It is always possible to be more inclusive – the point of the continuum – and a calm, quiet, orderly, predictable, clear classroom can still be exclusive if a teacher allows children who find stuff harder than others to flounder.
3. Classrooms are compromises and more should be made in favour of those who would otherwise struggle most.
Designing any system that perfectly meet everyone’s needs is impossible because the interests and preferences of individuals are often opposed to each other. Trying to meet them all usually means nobody getting what they need.
The most able and knowledgeable children may prefer to learn independently but given how children are organised into classes allowing this for them means allowing it for all, and this has a negative effect on other children, and particularly those who find learning hardest who need the most direction and guidance.
A good example of this is the range of the primary curriculum and the size of the GCSE curriculum, which are too large.
A big curriculum is benefits those finding it easiest to learn because to cover all of it teachers must go too fast for those who struggle. At the end those finding learning easiest are those who gain top grades and access to more prestigious, high-status destinations. Those that find it hardest are least likely to see beauty or purpose in what they do and most likely to leave with qualifications of little practical use or value.
The purported purpose of SEND designation and – even more so EHCPs – is to balance this by requiring teachers and other education professionals pay more attention and afford more resource to these children than others. In many cases there needn’t be too much of a tension, and strong foundations make it easier for schools to identify and support the children who need help the most.
But while what works for all children usually benefits those with additional challenges most there will still always be children who require decisions to be made assertively in their favour even if this means others losing out.
Sometimes this is easy to see and straightforward to implement.
If a child with a hearing impairment needs to sit on the centre of the front row, then this need clearly outweighs the need of other children who might learn more if they sat there.
Similarly, if a visually impaired child requires a worksheet is blown up to A3 it would be unacceptable for the teacher to refuse to do it because it adds to their workload.
More difficult is – for example – what a teacher should do if almost all their class is ready to write an essay but some do not yet have sufficient mastery of the content to do it properly.
What should a teacher who wants to be more inclusive do in a situation like this?
Here teachers often – maybe usually – go with what they perceive the majority to be.
If most children are ready for the essay, then it’s time to write the essay and those that aren’t must muddle through as best they can.
Compromises like this may seem to be appropriately utilitarian in how they appear to be what’s best for the greater good, but they clearly favour the already advantaged most, which is uncomfortable because it is inherently inequitable.
This is a danger inherent in all societies and was written about well by John Stuart Mill – his arguments were latter summarised in the phrase “The Tyranny of the Majority”, which is what happens when what is best for most of a group is exclusively prioritised.
A more equitable compromise might be more pre work for those who aren’t ready even if this means some children must wait before beginning if the general conditions aren’t conducive to allowing some children to start while others receive more instruction.
Once children are working on their essays a more inclusive teacher would target individual support on the children experiencing most difficulty. This is equitable decision making because while the children finding the work easiest would also benefit from greater personal intervention, those struggling most lose out more if they don’t get help.
There’s nuance here too, and the concept of a continuum becomes important again.
Children aren’t either included or excluded in learning – they can be more or less included and including a child who grasps things easily more by, say, providing the class with more in-depth material or going at a pace that best suits them means those who struggle more are included less.
This might make them and their families happy, but it comes at a greater cost to those who struggle more, so it’s more equitable to make more decisions more in the interests of those who find learning harder especially when the system overall is slanted towards those who find it easiest.
This at scale would probably means trying to cover less.
This may seem radical but is not a fringe view – it’s one shared by Dylan Wiliam, emeritus professor at the UCL Institute of Education too.
None of this can be effective if strong general conditions aren’t embedded, and this is a mistake teachers can make through the best of intentions; if, for example, a class slides into talking and other off task behaviour when their teacher moves to individual support then this individual support won’t be effective and the result will probably be a-deterioration in general standards, which will affect those who struggle most making any individual support they receive ineffective.
Another helpful way of looking at this for classroom teachers is to first consider core principles of good instruction in general and then take steps to make sure every member of their class benefits from them, not just those who find learning comparatively easy.
Rosenshine’s Principles – adopted by many schools and teachers as a helpful heuristic for effective teaching – is a good place to begin.
Let’s explore just one – secure a high success rate.
This is easier to do for some children than others because of different starting points and differing learning abilities. Here a teacher who is being less inclusive might move on to new material after checking for understanding techniques show only some children have learned most of what they have just taught.
This is exclusive to children who have not achieved a high success rate because it means the teacher moving onto new material before they are ready. This means they can’t move onto the next stage – almost certainly in hierarchical subjects such as maths – and are excluded from the point at which they lost the thread. A teacher who is being more inclusive would spend more time responding and re-teaching so more children were able to secure a high success rate and be ready for the next stage.
And again, in this instance generally better teaching for all is likely to be inherently more inclusive because if – for example – explanations have been well sequenced and rehearsed to clarity then more children will achieve a high success rate meaning fewer requiring re-teaching and the teacher able to be more targeted and effective with those that do.
This is messy and complicated – and the only people able to decide what and how compromises should be made are classroom teachers as nobody else is close enough to the problem.
While it can be tempting for leaders and others to try and micromanage this, it doesn’t work.
4. Teachers should be in control of the decisions they make.
Children do not usually get a SEND identification in the same way unwell people receive a medical diagnosis.
They are assigned the label for many different reasons in many ways, and there are good reasons to be cautious about assuming there is shared meaning of the terms used.
There isn’t a standardised process or agreed criteria for adding a child to a school’s Special Educational Needs Register.
In many schools there is probably more process and procedure over buying a new laptop computer.
Indeed, the most significant predictor of whether a child is identified with SEND is the school they attend rather than anything about them.
We don’t know how much children identified as having SEND have in common with each other.
We don’t even really know who they are, and we don’t know whether they have enough in common to be grouped together at all.
Theoretically subdivisions such as “learning difficulty,” “cognition and learning”, and “social, emotional and mental health” should bring signal to the noise, but often they don’t because they too have no shared meaning; one setting might identify a child as having a cognition and learning difficulty, whereas another might not assess them has having a special educational need at all.
In practice a designation is made because a child isn’t attaining as highly as peers and nobody really knows why.
This makes it quite possible for a child to be identified as having special educational needs because they’re summer born, missed a lot of school or even because they’ve had limited access to good teaching.
Much of the information available isn’t secure enough for teachers to make decisions on without drawing on other evidence – most importantly what they notice about the learning of the child in their classroom. It means they can’t assume advice they are given on how to teach – say – children with cognition and learning difficulties is relevant to children in their classes because they can’t be certain the terms and criteria mean the same thing to everyone working with that child.
Similarly, while recommendations made by non-teaching professionals such as educational psychologists, counsellors and speech and language specialists can be useful, these recommendations are often not contextualised to the specific conditions in which a teacher encounters a child.
And this matters.
It’s striking how dissimilar the experiences of different teachers teaching the same child often are and the reasons for this can have little to do with how closely an individual plan is being followed.
This doesn’t mean teachers who want to be more inclusive should ignore information made available to them, but they should be allowed to be wise arbitrators of how best to use, interpret and apply advice, within legal frameworks meaning there are instances in which they must follow some directives for good reason.
The ability and capacity of teachers to do this varies, but nobody is capable of better decisions because nobody else is in the room with that child in that setting at that moment in time.
This is inevitable, and there’s nothing anyone can do about it even if they wanted to.
Ultimately, schools are set up for teachers to work with classes, and this means they must make minute-by minute decisions about how best to teach and include all pupils.
Micro-managing and imposing numerous and specific directions on them as to how to do this may be well-meaning but fails to account for the infinitive complexity within which teachers must work even if the way their pupils learn is mostly the same. It also invites in performativity; doing stuff not because it is really in the interests of children but to appease and satisfy other adults.
Where the evidence base is secure this might work but where it is not it doesn’t.
Better to empower and educate teachers to make better decisions than try and make decisions for them using incomplete and flawed information detached from the classrooms they work in.
5. Inclusion is the main business of classroom teachers.
Inclusion is primarily the business of classroom teachers.
Nobody can do it for them.
Attempts to try will fail.
“Inclusion” can’t be done by a SENDCO and Teaching Assistants alone – indeed this is a common concern and complaint of those who work with children identified with SEND who can often feel they are marginalised and siloed as if the education of a potentially hundreds of young people were only their responsibility.
There are just too many children who need great practice for a discrete specialised department or strategy to ever meet need.
Inclusion cannot be done by a strategy or policy document, or an IEP or a pupil passport or an EHCP.
Classrooms can only be made more inclusive by teachers, and they can only do this if they see the education of every child as their responsibility. They need practical support and help that makes it easier for them to fulfil this responsibility. This support must be clear and respectful of the contexts in which they work because when it isn’t it is too easy to think inclusion is too difficult and devolve responsibility for thinking about it to others. Support they get needs to start with the basics – leadership that makes schools calm, safe places in which there is room to think and decisions aren’t made in response to crisis.
Support should be dialogic and open to the possibility it might need to be changed and adapted when teachers find it isn’t helpful.
Inclusion – even when it is the first word of a completed sentence – is a verb not a noun, and teachers are the only people who can do it.
It must change as children and circumstances change. It must be worked on every minute. It is at the centre of good teaching, and teaching is not good if it is not inclusive.
It doesn’t need to feel mysterious or too hard to do, because most of it is about being a good teacher and seeing all pupils of equal value and having the same entitlement to learn. Seeing them as having more in common with each other than different.
I know to some this is a threat and must respect that, but to me it isn’t.
I don’t want either of my children to be thought of as special if this means being seen as fundamentally different to other children.
I want them to be seen as I and the people who know them best see them – perfectly normal, healthy human children requiring the things all children need to be happy and included in learning at school.
We are lucky, I know.
My children go to a school that understands this and sees inclusion in learning as a right both have – that respects the inherent humanity and value of all children.
This protects us from the SEND system which is failing everywhere.
It makes it matter less if documents are copy-paste terrible, the appointments cancelled, the advice inappropriate or even plain wrong – because the teachers are good teachers, and their values mean they include both my girls as much as it is reasonable to expect any child to be included in a system in which compromises must be made.
My final point is – I hope – the logical culmination and expression of the previous four.
Inclusion is primarily the business of classroom teachers and nobody can do it for them.
While the superstructure around inclusion can obscure this it does not make it any less true.
“Inclusion” can’t be done by a SENDCO and Teaching Assistants alone – indeed this is a common concern and complaint of those who work with children identified with SEND who can often feel they are marginalised and siloed as if the education of a potentially hundreds of young people were only their responsibility.
There are just too many children who need great practice for a discrete specialised department or strategy to ever meet need.
Inclusion cannot be done by a strategy or policy document, or an IEP or a pupil passport or an EHCP.
Classrooms can only be made more inclusive by teachers, and they can only do this if they see the education of every child as their responsibility. They need practical support and help that makes it easier for them to fulfil this responsibility. This support must be clear and respectful of the contexts in which they work because when it isn’t it is too easy to think inclusion is too difficult and devolve responsibility for thinking about it to others. Support they get needs to start with the basics – leadership that makes schools calm, safe places in which there is room to think and decisions aren’t made in response to crisis.
Support should be dialogic and open to the possibility it might need to be changed and adapted when teachers find it isn’t helpful.
Inclusion – even when it is the first word of a completed sentence – is a verb not a noun, and teachers are the only people who can do it.
It must change as children and circumstances change. It must be worked on every minute. It is at the centre of good teaching, and teaching is not good if it is not inclusive.
It doesn’t need to feel mysterious or too hard to do, because most of it is about being a good teacher and seeing all pupils of equal value and having the same entitlement to learn. Seeing them as having more in common with each other than different.
I know to some this is a threat and must respect that, but to me it isn’t.
I don’t want either of my children to be thought of as special if this means being seen as fundamentally different to other children.
I want them to be seen as I and the people who know them best see them – perfectly normal, healthy human children requiring the things all children need to be happy and included in learning at school.
We are lucky, I know.
My children go to a school that understands this and sees inclusion in learning as a right both have – that respects the inherent humanity and value of all children.
This protects us.
It makes it matter less if documents are copy-paste terrible, the appointments cancelled, the advice inappropriate or even plain wrong – because the teachers are good teachers, and their values mean they include both my girls as much as it is reasonable to expect any child to be included in a system in which compromises must be made.