My son is pretending to be a puppy. We’ve just finished looking after my sister in law’s dog, so both boys are very interested in all things canine at the moment. I’m resistant to getting a new dog, but the whole dog sitting experience may just have been a clever ploy by the rest of my family (led of course, by my wife) to make it happen. I’m not about to give in! Besides, B is doing a perfectly passable impression of a dog himself: running, barking, eating things off the floor, chewing things he shouldn’t. I ask him what type of dog he’s pretending to be. He answers, “I’m pretending to do a law course.” I am totally thrown by this, and only later learn that he means lure course. Apparently this is a feature of Nintendogs, which he has also been playing. Anyway, the point is that he is fully involved in this pretend play, which raises a question. Since when did my autistic son become so imaginative? Isn’t a lack of imagination a hallmark of the condition?
The answer is no. People on the spectrum can be highly imaginative, as I’m sure anyone with experience of autism will testify to. My son is increasingly imaginative and engages in all sorts of play, both on his own and with his brother. I’ve often found this a rather contradictory and confusing aspect of autism, until a recent lightbulb moment, when an important distinction was made clear. Children and adults on the spectrum often struggle not with imagination, but with social imagination. This is an important difference. Social imagination is a person’s ability to predict what others are thinking and feeling, to imagine and predict what might happen next, to understand the consequences of what is said and done in a social situation. This makes a lot of sense and explains the difficulties many people on the spectrum have with dealing with people and what to them can be the unpredictability of social interaction.
I was feeling pretty stupid for not making this distinction before. I must have read it a hundred times without ever letting it really sink in. Then I read a recent thread on Mumsnet, which sought to clarify the distinction between imagination and social imagination. Thankfully, I am not alone in my misconception. Many of the commenters on the thread spoke of how their asd child was also highly imaginative and how it went against their preconceptions. The thread is worth a read, as is the blog link on it.
So yes, my son is imaginative. But what of his social imagination? How is he with people? Without a doubt, my son is a friendly, gregarious little boy. He will talk to anyone. As I write, I am in a children’s soft play area. I cannot hear B, but I can see him. He is talking to an adult stranger, although I cannot work out what he is saying. I have no doubt that it is a very one way conversation. B will be talking, no doubt, about cars. He may have asked the stranger what she drives, but that will be the only give and take in the conversation. The rest of the conversation, if it can be called that, will be a monologue by my son on his current favourite make and model. He will not read the stranger’s expression, not pick up on her body language (or bemusement/lack of interest/annoyance) and give her few opportunities to join in. He will not understand the rules of conversation because he lacks the social imagination to do so. It is a very typical, very common scenario. B will talk to anyone and is not shy about starting a conversation. It must, of course, relate to whatever his special interest is. Try to steer the conversation elsewhere and he will simply wander off. He is brutally honest in that respect.
When it is time to leave the play area, I notice B has a small toy, the sort you get in a plastic egg from a vending machine. “Where did you get that?” I ask. “From the machine.” he answers. “Where did you get the money?” I ask. “From the lady.” he replies. Here’s me thinking he was talking about cars. He was actually tapping her for 20p. Which she gave to him. Words fail me.
While I’m on the subject of the indoor play area, let me share another little anecdote. B is in the under 3s only area (he’s five, but keeping him out of there is a relentlessly thankless task). He is climbing along the edge of the area, but there is a girl in his way. The mother of the girl is sat on the table next to me, but is unaware it is my son. “GET OUT OF THE WAY! NOW!” screams B (with no thought of how she might feel). When she doesn’t move, he screams at her again. Realising he is potentially psychotic, the girl runs to her mum. “That boy is shouting at me” she whines to mummy (the little sneak). The mum asks why, to which the girl answers, “no reason” (clearly there was a reason- she was in his way). “If it happens again, tell me. I’ll soon deal with him” she threatens. At this point, B ambles over to me. The woman, sat next to me, falls silent. Awkward.
My son’s difficulty with social imagination can be seen in a number of other ways. He is an excellent reader, but his comprehension of situations in books (specifically fiction) is poor. He struggles to describe characters’ reactions and interactions, motivations and likely responses. He cannot tell me what a character might be thinking or feeling, beyond the most basic of (usually visual) clues. It’s little wonder that he prefers non-fiction so much. He also avoids the type of play that involves characters interacting. We’ve bought him many toys over the years that might encourage this, such as Playmobil sets with families. The characters get ignored, but he will, predictably, play with the vehicles. It’s difficult as a parent to relate to this. Playing imaginatively with toys such as these had been such a huge part of my childhood. My son plays differently.
I can clearly remember when B’s lack of social imagination was first pointed out. It seems like a lifetime ago but it’s been less than two years. We had our first appointment with a speech and language consultant. We had concerns over his apparent speech delay and concerns had been raised by his nursery. But the consultant seemed less concerned with his lack of speech than she did with his lack of interest in the toys in the room. He had an intense interest in the drawers, filing cabinets, stationery and computer in the room, but was oblivious to the teddy bear’s picnic she had set up. Part of the assessment involved imaginative play with the teddies (pouring drinks, serving toy cake etc). My son had no interest. He didn’t want to say hi to the teddy, he didn’t want to put them in the house. He didn’t want to look at them and he wouldn’t look at the consultant much either. He quickly became restless and agitated and bored, but I knew what to do. I took out my phone and handed it to him. He immediately immersed himself in pressing buttons and making things flash and beep. It was a lightbulb moment for the consultant. The delayed speech, lack of imaginative play, intense interest in buttons, the restlessness. It all added up. By then, we’d done the maths too. We didn’t need to be told he was autistic.
As I recounted the details to my parents later that day, I cried a little. My mum and dad understood that I was upset, but I doubt they could comprehend why. They could not equate what I had told them with the (rare) sight of their son in tears. They did not know what this meant, in the way that I knew what it meant. This was probably around the time we first used the word autistic in connection with their grandson. They are still trying to work out what that means now, let alone back then. It was difficult for me to make them see the implications of what the health advisor had observed, the enormity of my son’s inability to interact socially. My parents have not seen me cry since that day.
This week I have been reading ‘Look Me in the Eye’ by John Elder Robison. The book is a memoir about growing up with Aspergers, and the difficulties encountered. Robison describes how, “People with Asperger’s or autism often lack the feelings of empathy that naturally guide most people in their interactions with others… I have learnt that kid’s with Asperger’s don’t pick up on social cues. They don’t recognise a lot of body language or facial expressions. I know I didn’t.” Clearly he has struggled throughout his life but at the same time, despite the lack of social imagination, Robison is clearly a very imaginative person. He is able to write a compelling story and has carved a very successful pathway through life for himself. This gives me hope.
Despite the problems that a lack of social imagination can bring, it is difficult to think of it as a disability, at least not yet. My son is at the age when this lack of social understanding and imagination makes him an utterly charming, beguiling, adorable little boy. He knows no social barriers and therefore does not withhold his feelings or his reactions. He will race up to a familiar person and shout their name, grab their hand and, of course, talk to them about cars. It’s the same with strangers. I watch people as they melt in his company, charmed and disarmed by his utter lack of self-consciousness. He’s easy to fall in love with and popular with the staff at school.
The time may soon come when B’s lack of social imagination causes problems. He may begin to crave, but not access, close friendships with other children. He may become conscious of his own differences, of not fitting in. We also need to instill in him an awareness of ‘stranger danger’. He lives in a world of complete innocence and sadly, but necessarily, a little bit of reality may be required. I worry about him.
For now though, I think my son benefits, rather than suffers from, a lack of social imagination. My eldest son told me recently that B is “famous” at school. Everyone knows my boy. You can take that to mean what you want; perhaps ‘infamous’ would be more appropriate! Of course, he’s oblivious to his fame. To him, the world is a playground. He doesn’t have time to stop and think what people may think of him. Most of the time, he’s too busy enjoying himself. Wouldn’t you like to be like that?





Do you know something your posts hit the mark every time. I have often wondered about this too as in my eyes small boy uses his imagination every day . However when i think about it its not in the social way. Btw ,when small boy was having his autism assessment the consultant set up a scenario with a few wooden toy people and made one fall down a ladder. Small boy ignored the little injured wooden person’s cries for help completely and proceeded to take great pleasure in enhancing his injuries somewhat by reversing over him twice with the toy ambulance provided.Its worth adding that there was lots of jottings made at this point. Lol .
Perhaps Small Boy was imagining it was another annoying health care professional! Thanks for sharing and putting a smile on my face x
What a great post and yes, once again you have hit the nail right on the head. Our children do not lack imagination. Nor do they lack empathy as is so commonly perceived. I read ‘Look me in the eye’ a few years ago now and I loved it. To me Robison’s way of explaining his life made perfect sense. And like you, I have often watched my son while his been enraptured by simple things, like sunlight reflecting on a window, and thought, how lovely it would be to be able feel that same degree of delight in the simplest of things.
Thanks. Aspie Kid posted a very interesting tweet today: Mind blindness (the inability to read minds) is not lack of empathy (the ability to feel what other people feel).
Thank you I will check it out.
I have two sons on the spectrum and this almost perfectly describes the struggle I have to explain their behaviour to other people. I am probably also on the spectrum but all three of us have different ‘ways’ with social imagination. I am desperate not to get it wrong, it actually causes me great distress and I apologise frequently for things I haven’t even done! My empathy level is off the scale and I put everyone else above me. My older son has absolutely no empathy, no understanding of how his actions impact others and his sole focus is himself. In the summer he shoots water guns at the local kids then goes bananas when they do the same to him. In the winter he throws snowballs but turns murderous if any are thrown at him. It’s so hard for other kids to understand, is it any wonder he has no friends? My younger son enjoys a luckier scenario as he has a very sociable twin brother who reels in friends and keeps them there for both of them. This is something he does naturally and I hope it will mean that my youngest doesn’t end up socially ostracised like his older brother.
From our experience there is no ‘one size fits all’ with ASD, I like to think of it as a buffet where everyone gets different things on their plate in different quantities but we’re all at the same function!
I absolutely love the buffet analogy! I will absolutely be stealing that one for myself!
Yes, I also struggled with the misconception that ASD means lack of imagination. My girl can pretend she’s a mermaid, dress-up and “talk like one” but she has not the social imagination to predict people’s reactions if she turned up to a birthday party dressed and acting like one.
It’s funny that you also mentioned several similarities between our children that I described a few years ago to a child psychologist as early concerns about E.
She used to ask strangers to fix her hair and take her to the toilet (which could be frightening if you lost sight of her at Pontins only to find that some random had taken her there.) She would talk about Princess Peach to any passer-by assuming that they also knew everything about her. She was also “famous” at school but at the same time curiously friendless. I was virtually laughed out of the psychologist’s office with the suggestion that I need a referral myself and it was obviously my fear of her embarrassing me that was the problem. He also seemed to be suggesting that i had looked-up the symptoms of Autism and was applying them in some Munchausen’s way to my daughter, whom along with myself, had barely been near a doctors office in years. It still shocks me to think that a parent’s concerns for their child could be dismissed in such a cack-handed manner by a mental health professional.
She no longer does these things as fortunately it was possible to utilise her reluctance to go against rules (do not approach strangers only “safe strangers” etc.) now she will still “talk at” people somewhat but its more with shop assistants and lollipop ladies now.
The biggest concern I think we all have as parents is the point when these traits/differences stop being endearing and “cute” to people and therefore less accepted or god-forbid cause them to become a target. This has been happening for us recently and
it is scary for many reasons one of them being that they themselves start to become aware of people being mean but not knowing why or how to handle it. I will do all I can to teach her to be proud of who she is because I never want her to start to hate herself which I can see happening as she gets older. I know i won’t be able to protect her from everything but if I help her to accept and be proud of her differences others a surely more likely to accept her too.
I find the future a scary place for similar reasons. Like you, I hope I will be able to instill self esteem in my boy. It sounds like you and your daughter are making good progress. Long may it continue this way x
Thanks for putting the link to my blog! (I didn’t realise it was mentioned elsewhere on Mumsnet).
So much of what we learn from aspergers is learned on the hoof, because we’re all different in so many ways. I really dislike generalised statements about aspies and what they can and can’t do! As I’m sure lots of other parents do too.
As an aspie myself, I’ve come to a new understanding of this difficulty with social imagination and am glad it’s struck a chord with people. Having said that, it would be so nice sometimes to flick a switch and know what to do! X
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I’ve just discovered your blog and really, really enjoyed reading this post and all the other replies. Your description of B sounds so much like our 13 yr old son J who is funny, charming and lovable, vulnerable and naive, intelligent and creative – as well as incredibly infuriating and totally ego-centric.
The reference to ‘brutal honesty’ reminded me of recently when my husband tried to have a ‘serious talk’ about an ‘incident’ at school when J prodded a TA in her chest area to get her attention. My husband tried to explain why the TA might not have liked him touching her like that but sensed that his talk was not making much of an impression as J appeared to be far more interested in playing with his Dr Who figures. My husband (a bit irritated) said to J in a sarcastic tone (completely wasted on him might I add) “Am I boring you?” To which J replied; “Yes, a bit”.
My youngest Son Oliver was diagnosed with Autism on 1st October so this is all still very new to our little family. Later that week, my Mother passed away so i’m not going to forget that week anytime soon I can tell you!
So much of what you describe in all of your posts really resonates with us though. My wife often says that you could be describing us, only three years into the future. Of course we have no way of knowing where we will be that far down the line, but your experiences with B often strike a chord with us, and we can usually find a similar example of how Oliver’s behaviour in social situations can be inappropriate. It is endearing to strangers right now as he is 2 and cute, so he gets away with it, but will the same be true when he is 8 or 10 and he goes up to a complete stranger and tries to cuddle them?
His imagination is certainly there though, I have no doubt of that, and all of his therapists have quickly concluded that he is a clever little boy, very capable of manipulating events to suit his needs. Social imagination as you say is a very different thing however and we most certainly need to try and help him with this.
Thanks for posting. We will continue to read that’s for sure!
I ran across your blog and have read with much attention. I do not have a child with Autism…..to my knowledge, and I say this because now that my kids are 28-26-25 I sometimes wonder. They had struggles with anxiousness and inability to cope in stressful situations, which caused them much pain…along with many other difficulties that has made, their lives harder. I am in no way comparing to your struggle and I will pray for daily life to level out for your son. I just wonder at times that I may have missed something along the way with them. The symptoms I read are very familiar, maybe there are less levels that they have had, I dont know really…I just know that they still struggle with anxiety and throw in an awful drug use to deaden the pain……This has nearly killed us…..but I enjoy reading, enjoy may not be the right word…..appreciate might be better. Thinking good thoughts for you all….preacherswifeintheknow
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