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In which I try to handcuff the wind

Today, today as I write this, probably not today when I publish this, right now, I am having emotions . This is a fairly normal thing, right? We're living breathing animals, we have emotions. However, I find it confusing. Some emotions I've managed to more or less pin down: dreading, pleased, frustrated, comfortable, neglected, some others. But many others, I don't truly understand, they are vague and nebulous, just a... feeling, that's affecting me in some way. As I write this, I'm trying to focus on the emotion I'm going through. It feels tense. It has elements of frustration. I'm also a bit tearful. More than anything, though, I feel disconnected, that I've broken free of my moorings, that my brain isn't tied particularly closely to reality. It's unsettling. It's not a feeling of physical disconnection, or disembodiment - I'm fortunate enough not to suffer with that - but more that sensory perception is almost overwhelmingly magnifi...

A little more about interviews and jobs

Nothing that I specifically need to add, just wanted to link to this, because it is such a model for how companies can act when it comes to hiring autistic people. https://www.campaignlive.co.uk/article/why-microsoft-hiring-autistic-talent-drive-creativity/1458408   Speaking at the #DiverseMinds conference in London today (1 March), Michael Vermeersch, digital inclusion lead at Microsoft, said that the company’s drive to hire autistic talent has an 80% success rate.  Sharing what he described as "the greatest feedback he had ever received," he explained how one such employee had stated: "For the first time in many years I feel like it is not a weakness to have a disability." An open policy Microsoft launched a pilot project to hire autistic people in April 2015. According to Vermeersch, when Mary Ellen Smith, the corporate vice-president for operations, spoke at the United Nations about a pilot scheme the company had launched to employ people w...

A brief note on terminology

The language of autism, or rather, of describing autism and autistic people can be vague and shifting. After all, both the science and the community are developing. And I don't claim this to be anything other than my view; nevertheless, sometimes words are used which bother me a bit, and I'd like to address that. Asperger's Syndrome : was a diagnosis first introduced in 1944, and removed from widespread medical usage in 2013. As with many obsolete medical terms, increased understanding meant that its definition was no longer felt to be accurate. However, many people diagnosed with Asperger's during those seven decades are still very happy to identify with it (or the colloquial Aspie), and I'd not criticise that. That said, if you don't personally identify as having Asperger's, or you're not talking to/about someone who you know does identify that way, then it's best to avoid the term. Autistic Spectrum Disorder : is the medically accepted term. I...

The employment gap

Here's a link: http://www.autism.org.uk/get-involved/media-centre/news/2016-10-27-employment-gap.aspx Think a moment about the stat. 16% of autistic adults in full-time work. Sixteen percent . That is desperate and shameful - and it doesn't even consider how many of those lucky sixteen percent are able to fulfil their potential and develop their career. Another link: https://www.wearethecity.com/nine-ten-uk-companies-not-considering-neurodiverse-candidates/ If only 10% of workplaces make accommodation for neurodiversity, that inarguably presents an obstacle to autistic and other neurodiverse people, it will contribute to the employment gap, and any proposals to address the problem should be both welcomed and encouraged However, it only gets us so far. Before adjustments can be made to help an autistic person in the workplace, they have to be in the workplace . Granted, very few people enjoy interviews and assessment centres, whether neurotypical or not - but for aut...

Time to talk

Today is Time to Talk day, run by the campaign Time to Change. And I want to talk about this. Of course, as you're reading this, it's not Time to Talk day (that was February 1st); it's taking me a while to get this blog together, I'm not a spontaneous person, things take time and they take preparation. I promise, however, that I am sat here writing on the relevant day. Firstly, and above all else, I need to clarify something: I have no objection to Time to Talk. It's a great idea. It is hopefully benefiting many people, encouraging those with a wide range of mental health issues - or those affected by such issues in others - to find support from friends and family and colleagues. It is an important thing. It is a good thing. Far too often, we are afraid to discuss mental health, because of the stigma attached. I won't go into that matter here, better to link to the official site: https://www.time-to-change.org.uk/about-us/our-impact . So yes, it's a g...

I get pissed off by a tweet

This is by no means the worst thing I've read about autism: Nevertheless, it struck a nerve, and pushed me over the line from 'maybe I should write a blog' to 'yep, definitely need to start writing a blog'. Over the past year, I've found myself increasingly assertive in opposing misconceptions and lies about autism wherever I find them. At the heart of these, so often, is the idea of autism as a disease - one you can catch, one you can perhaps cure. When this rears its head, you'll often find scientifically-literate folk fighting back - and I'm glad they do, it's important work. However, there's a personal perspective that I always want to add, something very simple yet so often overlooked: I am not a disease. Look at that tweet. It's not shouty and crazy, it's not full of woo. In a very level and apparently considered (if scientifically nonsensical) manner, it presents autism as a dreadful condition that one can catch from a p...

I decide to write a blog

Before we began with the questions, and there were a lot of questions, I was told how it would work: the questions, then I'd go out into the waiting room for a while whilst they discuss my assessment, reach some conclusions, and if there was any uncertainty, I'd be asked to come back for further questions, further assessment. Certainly, the impression seemed to be, that second stage of assessment was more likely than not. Then the questions came, and I answered best I could, and as planned, I was asked to wait outside. No sooner had I sat down than they called me back; diagnosis of autism, no further assessment required, not borderline, clear as day, autistic. Lurch back eight months: a helpful therapist called Liz, a curious rounded room in the turret of an odd-looking building, asking me if it had ever been suggested I might be autistic (no, never). I did some informal tests, was put on a waiting list, eventually got that assessment. But Liz told me something else, she to...