The other day, someone on Twitter - an autistic person who doesn't experience them - asked me what it feels like to have a meltdown. It’s not a subject I especially like talking about - I’ve attempted to write about it several times on this blog, got frustrated, and given up. This past week, I … Continue reading On meltdowns
Nothing makes me a more committed proponent of the Social Model of Disability than modern lighting. I am far more disabled, as an autistic person, than I once was. I'm far less tolerant of sensory triggers than I once was. Noise and bright lights are the things that get me more than anything, and more … Continue reading Modern lighting is rubbish.
Over a decade ago, when I was working as a low-level administrator in a university student support unit, I remember a student who was a regular and frequent visitor to our service. He came in virtually every day. He spoke in a staccato, "mechanical"-sounding voice. He always wore the same choice of clothing: blue outdoor … Continue reading Why I “can’t possibly be Autistic”, Reason #3: I’m not THAT rigid, right?
Wearing sunglasses helps me cope with noise. And yes, I do mean noise in an auditory sense. But this doesn't have anything to do with synaesthesia which, to the extent I've analysed myself and my perceptions of the world so far, is not something that I experience. Over time since my diagnosis, I've reflected and reflected … Continue reading I wear sunglasses to deal with the noise.
[Author's note: I'm publishing this post almost simultaneously with a previous one because I had both stored up as drafts in my paper notebook, but hadn't had sufficient "get-up-and-go" to publish them until now. This is the more recent of the two.. However, I felt that the other post was sufficiently time-specific to need publishing … Continue reading It’s never all bad.
I talk to myself. An awful lot. When I do this, I'm almost invariably verbalising my thinking about, and processing of, the thing I'm doing at that particular moment. This isn't the same as the inner monologue that runs incessantly over everything that I do; the one I hear at every waking moment, but which … Continue reading Director’s Commentary
[Feature image description: close-up view of the trunk of a Weeping Willow tree, viewed from behind the metal railings of a bridge, diagonally leading away from the bottom left to the top right of the image. The tree is resplendent with masses of bright green leaves hanging downwards. Behind the tree and its branches, a … Continue reading The same crap, on top of everything different
A while back, I wrote a rather lengthy post about social interaction, empathy, and so on, and how (in my opinion), every little bit of behaviour we see in front of us comes down to how someone processes information. I’m still banging on about this, because I still get repeatedly fed up with people – … Continue reading On ‘symptoms’
As I wrote in another post a while back, sometimes it hits me. And this morning it really, really hit me. And I did something I've never done before. Since my official diagnosis, exactly two months ago today, I've been – as usual – in numerous situations at work where I've been required to 'network'. … Continue reading A line has been crossed.
I've been a little short on spoons over the past few weeks. Once the working day is over, and my children have got as much out of me as they need, my brain hasn't had sufficient processing power for me to blog, and I've struggled, even, with many everyday tasks. I'm all used up. I now feel … Continue reading The importance of self-care