Friday, 11 September 2026

Autism, the Holy Grail of education and chocolate-covered custard creams

After eight years of epic struggle (his first four years of school, before learning got less playful and required more sitting still and listening, were OK, good, even…), today marks the end of the first week of specialist autism college for 16-year-old Oliver.

It’s not just a relief for him. After eight years of defending him in meetings, representing him in meetings, advocating for him (and AuDHD in general) in meetings and battling for some level of provision and adjustment for him in meeting – and this is just one of my neurodivergent kids! – I we are done trying to fit into a one-size-fits-all education system. And I am, I realise, absolutely knackered. Thank god we didn’t have a fourth!

Image AI generated

 

A funny kind of thankful

And I’m grateful. I really am. Grateful to the council for funding his place (although, given that it was clear to everyone that Oliver needed specialist provision three years ago and they said no – leading to a cataclysmic breakdown and Oliver learning alone in a classroom from worksheets for the last two years – I think they were left with little choice). I’m grateful to the college for existing for people like Oliver. But, at the same time, I’m grieving for the life that 16-year-old him is not accessing.

At his college, there are literally six other students – in the entire college. (Just one of them is doing Sports Studies – one! Makes me wonder what possible sport he can be partaking in – athletics? Yoga? Walley?!)

Whilst Oliver couldn’t be dealing with large groups of people, busy corridors and sensory overwhelm, having so few students in the college allows for a very small friendship pool. And as everyone travels long distances to be there, even if he did make some good friends, he wouldn’t be able to freewheel off with them somewhere after college, as they all get picked up I taxis and whisked home as soon as the college day finishes.

I remember my 16 year old self and all the (mis)adventures and memories I made. It was probably the best time of my life. It’s sad that, for many autistic children, the choice is either overwhelm and autistic shutdown at a mainstream college, or shut off from the world and any chance of having those adventures and making those memories at a specialist setting.


Education's unobtainable Holy Grail 

I feel like the sentiments of this year’s SEND white paper, that calls for better integration of SEND students into mainstream school is, actually, the Holy Grail in all of this – if only it was possible.

·         Because teachers aren’t properly SEND trained and, even if they were, the extent of the curriculum, pressure to reach targets and reduction in classroom support would mean they don’t have the time or space in their teaching to accommodate different learning styles and needs.

·         Because secondary schools will still be huge, sprawling buildings that smell of cabbage and mashed potato, filled with echoing corridors and hundreds/thousands of other people.

·         Because learning will still, mainly, happen from the front of the class, through spoken word, written word and memorisation, because that’s the only way to teach en-masse when there’s one teacher and 30+ students – but these approaches don’t work for so many neurodivergent, visual learners.

·         And because, by trying to circumnavigate some of these challenges by having bigger SEND bases within mainstream schools you are, effectively, just creating mini specialist settings within mainstream schools. Turning the neurodivergent students into the ‘other’.

Honestly, I don’t know what the answer is, but surely there must be one? In the meantime, I’m just so relieved that I won’t have to be having any more battles with teaching staff and systems that don’t understand reasonable adjustments, and that Oliver can finally start learning about things that interest him and in a way that makes his brain come alive.

 

‘Not just’ any custard creams; Not just any family

Meanwhile, the eldest autistic in our family continues to drive me mad with his exasperating behaviour.

I mean, I absolutely advocate for autistic people and always will but, at the same time, living with their foibles – or at least my husband’s – can be infuriating.

Just yesterday, he admonished Oliver for eating two out of the packet of six chocolate-coated custard creams he’d bought from Marks and Spencer (for those who don’t know – it’s the Ritz of grocery shopping).

It’s a loss of control thing – he struggles with anything that takes control away from him and how he thinks things should play out…

Which, it seems, was him eating them all as, later that night, he took the (unopened) second packet of white chocolate-covered custard creams – arguably even better than the plain chocolate version – and ate not just two, but the lot (the evidence there for all to see in the bin the next morning)!

The hypocrisy is incredible! As is the complete lack of moderation or impulse control.

His reaction, on being discovered, was to go out and buy three more packs which he swears he won’t be eating any of. This is always what he does (this happens a lot) and, invariably what happens is that, they stay in the cupboard unopened (or opened with just one or two eaten) until, one night – normally when he’s a glass of wine down – his impulse control will go and he’ll eat them all again!


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