I suppose, people being people, that other Aspies have tried to explain how the condition affects their functioning in some way, such as difficulty reading non-verbal signals, only to hear, “I, like, get that too, you know: maybe I’m a bit Aspergers.” Even after ignoring the involuntary wince that is triggered whenever language is tortured in my presence, I struggle to respond to that. While I don’t want to dismiss out of hand the possibility that they might be correct, it can be hard to explain how AS (and autism) are  about more than being awkward in social situations.

What I want to say to these people – but can’t because my AS makes it too difficult to formulate an adequate response without zoning out for too long and dropping out of the conversation – is that I doubt very much whether they do have AS. AS is not like a salad bar where you get to choose how much of each symptom you want. It’s not something I chose to have – I have it, live with it and cope with the challenges as best I can. Each symptom taken in isolation does not define the condition: it is called a pervasive disorder for a reason. It is a set of symptoms, usually with varying degrees of severity, and having AS means you pretty much got the lot.

What is “the lot”? To quote the Wikipedia article which summarizes the DSM-IV diagnostic criteria,

[…] a pattern of symptoms rather than a single symptom. It is characterized by impairment in social interaction, by stereotyped and restricted patterns of behavior, activities and interests, and by no clinically significant delay in cognitive development or general delay in language.

This doesn’t even attempt to explain why these symptoms occur: it is just a “pattern” that recurs and has been labelled as Asperger Syndrome. The label is a convenience, nothing more, to cover the effects of particular cognitive differences. It does not describe the differences between individuals with AS, the varying degrees of difficulty we face in everyday situations. Couched in the most general terms it says nothing about how it feels from the inside – how exhausting it is to deal with “normal” life, to feel so often that we have to consciously act “normal” with other people so that we are not seen as alien, to face censure for “inappropriate” behavior when we don’t conform to their “normal” standards.

I doubt that any sighted person would describe themselves as “a bit blind” because they close their eyes occasionally. Likewise, they are not “a bit Aspie” because they sometimes feel awkward in social situations or have a fanatical interest in, say, football. There is evidence that the Aspie label is somehow becoming seen as “cool” – I can’t understand why this should be so, because I know first-hand that the reality is that even in a mild form it causes significant difficulties for those directly affected, and also indirectly for those such as partners in relationships.