Special Educational Needs Spending is Being Exploited by Middle-Class Parents
The Mail has a piece by Dr Max Pemberton about the deeply uncomfortable truth concerning special educational needs children in the UK:
A significant chunk of the money that should be spent on educating all children is being hoovered up by the special educational needs system, and it is increasingly being gamed by sharp-elbowed middle-class parents.
A report published last week by the think-tank Policy Exchange lays bare what many working in children’s services have suspected for some time. SEND (Special Educational Needs and Disabilities) spending has risen in real terms by 58.5% in the last six years, with a greater rise – 65% – in wealthier local authorities compared to poorer areas, where it increased by 51%.
Seven of the 10 councils that saw the biggest rises were in the most affluent areas, such as Hampshire, Kent and Surrey.
Since 2015, half of all new school funding has been spent on SEND. Let that sink in. Half.
Nearly one in five children in England are now classed as having a SEND need, and the number of EHCPs (Education, Health and Care Plans) has more than doubled since 2015.
You can find Policy Exchange’s report here.
As Pemberton explains:
There are children with profound and serious special educational needs who desperately need support. Children with severe autism, significant learning disabilities, complex physical needs.
These children and their families deserve every penny of funding and then some. The system exists for them but it is failing them. And that is the problem.
The problem, he says, are certain parents who are incapable of or unwilling to accept that their offspring might not be geniuses:
Some middle-class parents simply cannot accept that their child might not be that bright, or that sociable, or that talented. When two successful, high achieving parents produce a distinctly average child, the idea that their charge is just, well, ordinary is intolerable. There must be something wrong.
There must be a reason he or she is not top of the class. And so begins the frantic quest for a diagnosis, a label, something that explains why their offspring isn’t the genius they expected.
Policy Exchange’s Report (p. 8) states:
Despite clear evidence linking SEND needs to deprivation, spending has risen fastest in the most affluent 50% of local authorities. Over the six-year period average SEND spending increased in real terms by 65% in the 50% most affluent local authorities in England, whilst rising by 51% in the 50% most deprived council areas – a difference of 14 percentage points. 70% of the councils that saw the highest increases in SEND spending were in the 50% most affluent local authority areas. This inequitable growth, despite clear links between deprivation and SEND need, highlights how factors beyond natural increase are driving spending growth in the SEND system. Previous research by the Sutton Trust has found that middle class families were more likely to appeal to the SEND Tribunal to secure an EHCP and more likely to secure a special school place for their child.
Pemberton explains, and as usual you only need to follow the money:
It couldn’t possibly just be that not every child is exceptional. Far easier to get an ADHD diagnosis than to accept that your child finds maths hard because maths is hard.
What makes this worse is a growing trend of parents bypassing the usual assessment routes altogether by going private. NHS waiting lists for autism and ADHD assessments can stretch to years.
A BBC Panorama investigation in 2023 exposed how some private clinics were diagnosing ADHD after rushed online consultations. One senior NHS psychiatrist told the programme that almost everyone who paid for a private assessment was being diagnosed.
There is, of course, a clear financial incentive for private clinics to do this: parents are paying customers, and a diagnosis is what they are paying for. No diagnosis, no repeat business.
Local authorities are legally obliged to consider privately obtained reports, and many parents know this.
So they hire SEND consultants and commission independent educational psychologist reports at over a £1,000 a time, and if the council says no, they appeal to the SEND Tribunal.
It requires money, confidence and time – the kind of resources that affluent, entitled families have and that families in deprived communities do not.
This site has already carried pieces about this scandal by Mary Gilleece, for example on how SEND spending should be cut.
The Policy Exchange Report concludes:
The Government’s upcoming reforms must grapple with the funding challenges in the system. With the Government committing to assume responsibilities for SEND funding – and the deficits councils have accrued – from the end of 2028, placing the SEND system on a secure financial footing will be essential for public finances. The system cannot offer fairness to schools, families and young people with SEND if financial sustainability – and the reassurance that support can be sustained for as long as it is needed – cannot be restored as part of future reform.
The Mail’s piece is worth reading in full.
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I suspect that a lot of this isn’t needed at all and that in many cases, simply tolerating that some children are different despite they’re not per se less capable than the others would be sufficient. Example of that: When I was still in school, there was an environmental excursion into a large nearby wood planned (the Soonwald, Soon Forest, to be precise) late in the year. On the appointed day, the weather was terrible but the excursion went ahead nevertheless. The bus full of pupils ended up toppling over in a violent snowstorm. Naturally, this was a big topic of discussion at school and I opined that the excursion shouldn’t have been allowed to go ahead because of the weather but had been allowed to go ahead nevertheless because of a desire for environmental self-gratification by the responsible people. The specific term I used was Selbstbefriedigung, German for masturbation, but I didn’t know this at time. This was obviously immediately reported¹ to the responsible person, namely, the head² and was one of the many school scandals I caused more-or-less inadvertently by using words I meant in a certain way but whose actual meaning different substantially from what I believed… Read more »
Here in the UK, there are so many children with Special Educational Needs and Disabilities (SEND) that it is costing local authorities a fortune dealing with it.
The government and local authorities should provide “means tested” assistance to all those that need it with wealthy parents paying their way.
To alleviate future damage to children and the costs involved there should be a government investigation as to why there is a big increase of children with SEND.
Once the reasons or likely reasons have been discovered then something drastic should be done so that babies and children avoid the toxins that cause the health problems to protect them in the future.
Even if the harms are due to a genetic disposition to a particular toxin, then that toxin should obviously be avoided regardless of whether the toxin is in a vaccine or not.
You should really stop to abuse people with a perfectly normal but rare “different development” for your anti-vaxx-crusade. I’m comfortably older than most childhood vaccinations in use today. During my time, only vaccinations against polio, tetanus and smallpox were mandatory for children and even this only when they were already at elementary school.
If you think vaccines are safe and effective you’re on the wrong forum.
Saying that all vaccines have high risks of serious side effects is as wrong as saying that they’re all safe and effective.
Imo the vaccines that have been in use for 30 or more years are highly likely to be safe, meaning that the risk of being vaccinated is much lower than the risk of being unvaccinated. If the older vaccines caused high levels of behavioural problems there would of been a surge in diagnoses when they were introduced even though 30 or more years ago far fewer diagnoses were made regardless of the cause. It could also be the case that some of the newer vaccines are safer than others, btw I’m convinced the Covid vaccines are by far the most dangerous so far, or the vaccines may be relatively safe on their own but multiple different vaccines significantly increase the risks.
I now assume ALL vaccines are unsafe, I was not anti-vax prior to “Covid” but I was very pro-choice and informed consent! My last vax was I think a Tetanus in the 1990’s.
The incidence and massive increase in Autism, MS, Alzheimer’s, Dementia and a whole swath of other physiological and psychological conditions need full investigation and that must include any and all “vaccines”.
We know the Big Pharma companies have not been running some, and maybe all of their double blind randomised tests properly, and we know there are dangerous additives, such as Thimerosal (Mercury), Aluminium Salts and Squalene in lots of these shots.
Dr Andrew Wakefield, who I believe one day will be exonerated, initially noticed a potential link between a vaccine and illness, and flagged it to the appropriate authorities, he did not initially claim a definite link, he merely suggested there should be a proper investigation, and for that his life and career were destroyed!
I will never willingly take a vaccine or gene therapy injection ever! But that is MY choice, everyone must make their own assessment and choice – but they most definitely should do so!
That something correlates with an increase in increasingly dubious autism diagnoses means nothing. It also correlated with the end of communist domination of eastern Europe, ever more aggressive anti-smoking campaigns and a lot of other things.
People with autism – the fairly few who actually have it instead of getting a diagnosis for the benefits it others as favour by some doctor – are people. They’re not your political football you can kick around as you see fit to deal with something entirely unrelated you happen to be afraid of.
I do not claim anything about this fear, in particular, neither that it’s justified nor that it’s unjusitified. I’m not interested in getting pricked with needles but apart from that, have no opinion on the topic. But I’m tired of being regarded as something like an obviously defective workpiece everybody can employ for his own benefit as he sees fit and then discard once this benefit has been accomplished.
I don’t remember writing that.
“Some middle-class parents simply cannot accept that their child might not be that bright, or that sociable, or that talented.”
Some middle-class liberals cannot face the possibility that they injured their own children and that is why they are so fearful of RFK Jr and a link being found between vaccines and autism and that is why they hate him and pro-safe vaxxers so much.
I think a lot of them also can’t accept that their child is a brat who they have no discipline over. I’ve seen that in my own family (next generation down).
Everyone wants to feel special.
No-one should want to be diagnosed as such.
Yet here we are…
If everyone is special then no-one is special…
Or no-one is special until everyone is special.
Only people who aren’t special want that. It’s a great disadvantage to stick out of the crowd in any way because the crowd fears and hates that and treats those who do accordingly. See also the eternal “Vaccines!!1” discussion above, which is based on the core assertion that These people cannot be people just like us!
But we are.
When I was at secondary school I was crap at maths for a few years. Regularly bottom of my class in tests. My parents stumped up for maths tuition from a Church friend on a Saturday morning. He showed me how maths could be interesting (thanks Mr Justin S.). I went from bottom to regularly first or second. He inspired me. That’s what many kids need: Inspirational teaching. I don’t reckon my regular school maths teacher was so very awful – just not very inspiring.
And what is the benefit to society, the economy by “investing” taxpayer money – making them poorer – on children who can never give a return on that investment?
If parents want these “special needs” children educated, they should pay for it.
Totally agree, “wealthy” parents should pay. A lot of these “Disorders” are contrived, and people just want a label assigned.
Personally, I think I’d be embarrassed to admit my kids were inadequate and in need of special treatment.
In the modern upside down age we live in having victimmpoints gets you a pass at middle class dinner parties for your stupid children.
I have told this story before but at around 13 my son came to me and said I think I’ve got ADHD or autism (can’t remember which now) because I can’t sit still. I told him what you’ve got is called being a boy. I think he had seen other children getting all sorts of perks and wanted a bit of the action.
Needless to say he’s absolutely fine.
This behaviour has been going on for as long as children have diagnosed as ‘special’ in some educational way. If there are educational benefits to be gained the middle classes will hunt them down. We have neighbours whose child is now 40 and they spent much money and effort to get their son diagnosed as dyslexic so that he could go to an expensive private school with a specialised unit for dyslexic children. He really just wasn’t very bright.
There used to be a cartoon which said “You are working class and your child is thick. You are middle class and your child is dyslexic.”
Now that the categories for ‘specialness’ have expanded and monetary gains can be made it’s amazing it’s taken so long for this to be noticed. Sadly it’s the genuinely needy children who lose out.
Your last sentence is of course crucial and I was about to say the same thing. It’s not fair on the children who have genuine problems.