Cat McGill

Stimming for mental health

Yesterday was tricky. I was doing a new thing that I’d never done before, and which necessitated me being around lots of noisy children for a prolonged period of time. (Tap dancing in a showcase, if you’re interested.) When we got home, I told my husband that he was not allowed to talk to me until I came out from under my duvet. Up until now, my duvet has been pretty much my only coping strategy, and as life is going through a difficult phase I feel like I’m using it all the time. Often I get home from work and go straight to bed. I’ve been eating meals in bed. I’ve been working in bed. It’s good, because it does help me feel better, but it’s quite limiting, and it’s affecting my relationships with my family, particularly my children.

Read More »

Reflections on the year

I know it’s a bit early for the traditional ‘looking back over the year’ post, but I’m in a reflective sort of mood this evening, after randomly deciding to re-read a blog post which I wrote just after Christmas last year. Something strange and unprecedented happened this week in our therapy session; the therapist asked us to consider whether we could stop sessions for the moment, because we seem to be – touch wood – doing alright. Unfortunately Tickle hasn’t managed therapy for some weeks now, and it seems that he really isn’t ready for it at the moment, but as his behaviour at home is more or less OK our therapist seems to think that we should just get on with life for a bit, and then maybe come back later when he’s ready. It’s a strange idea, having fought SO hard to get in to therapy, and particularly because we both know that without it our family would have broken apart in a rather spectacular fashion… could we let go of this security blanket?

Read More »

Birthdays

Tickle understands birthdays much more than he used to. We met him for the first time on my birthday; we’d brought cake, and we shared it, and he sang Happy Birthday to me. That’s what birthdays were: cake and singing. Tickle moved in with us about a week before his sixth birthday. I still remember we had to practically drag him in to the toy shop to choose a present, and he literally pointed at the thing right in front of him. (He wasn’t that interested in the presents on the day itself, but he did sing to his cake quite a lot.) It’s my birthday tomorrow. Tickle is quite excited about that, because he knows there will be cake. I’m working early tomorrow, so as there won’t be time for presents in the morning we decided to do them this evening instead. Tickle was *extremely* excited about this, so much so that the excitement tipped right over in to getting really cross that he wasn’t allowed to open anything, and WHY NOT I GOT ANY PRESENTS??

Read More »

Grief

We had to have our cat put down yesterday. She was only two years old, so it came as a huge shock to all of us. We are all coping with it in our own ways; Fairy is distracting herself with books and writing stories, I am crying buckets and welded to my duvet, Husband is musing about getting a memorial wind chime for our apple tree. Tickle, however, has been the biggest surprise. Tickle, is demonstrably and unashamedly sad. Tickle doesn’t spend much time interacting with the cats, but I know he does love them, and considers them part of the family – whenever we go on holiday he tells me he misses them, and he’s still not quite sure why they don’t come with us. But that’s not why I am surprised by his grief. I’m surprised because it’s a really big emotion, and he is allowing it to exist in his body without feeling the need to block it out or run away.

Read More »

I say what I mean and I mean what I say

Autistic people aren’t supposed to be any good at communication. It’s this word that is always used – deficit – like there is something wrong or something lacking from the way we choose to communicate. Granted, autism is a spectrum, and some people on the spectrum do find communication difficult, and aren’t very good at it. But then, some people who aren’t on the spectrum also find communication difficult, and aren’t very good at it. I am *exceptionally* good at communicating my feelings, thoughts, opinions, and desires to other people. I say *exactly* what I mean, no more, no less. The trouble is, I have realised as I’ve got older, that most people don’t like this at all.

Read More »

A day in the life

My alarm is going off at 6.40am. I’m awake enough already to switch it off; not quite awake enough to hit snooze instead. Luckily, I have anticipated this and set a second alarm for 7am, which is when I absolutely HAVE to get up. I think I only woke once last night, to get up for the loo around 2am. I’m not sure if it’s my sleep apnoea or my age, or just stress, but I don’t often manage to get through the night these days. It’s unusual for me not to have woken again around half five, dragged to consciousness by the shouting in the next room. Perhaps Husband has done well at keeping Tickle quiet this morning, or perhaps I’m so tired I just don’t remember. We have been trying out something new lately, trying to teach Tickle that morning really doesn’t start at 4am, that his bedroom light stays off until 6am whether he likes it or not. We’re having mixed success. Well, I say ‘we’, but I really mean Husband, as he is the one who sleeps on a mattress in Tickle’s room. It’s been almost a year since we regularly slept in the same bed.

Read More »

Sensory issues?

I thought I couldn’t be autistic because I didn’t have any sensory issues. Then I remembered how much I hate stickers. Thin, shiny bit of paper that stick to your skin. Urgh. And then they peel up at the edges and when you brush up against them they make a flicking noise… it makes me cringe. I hate going on training courses where they make you wear name stickers. I have learned to tolerate it, but I will take them off as soon as I can. The trouble is, taking them off involves touching them, and then when you try to throw them away they get stuck to your fingers…

Read More »

Stimming

So here goes, the start of a self-exploration of what autism means to me. In this first blog I’m going to talk about stimming. The term ‘stimming’ refers to self-stimulating behaviours that are often used by people with autism or other developmental disorders. The most common one you’re likely to think of is flapping your hands – my son does this a lot when he’s excited! Some people rock, some people jiggle, hum, bang their head, make noises; there’s really no end to the variety of stims possible.

Read More »

Noise. (And a bit on music)

I’ve chosen noise as my next topic to explore as it’s one that fascinates me, and I haven’t quite got my head around it fully yet. I have a very mixed relationship with noise. I’m a musician by trade, and a music teacher. I LOVE noise. When I was teaching secondary music I could quite happily sit at my desk surrounded by a class of thirty kids playing keyboard while I marked my A level essays, and still be able to pick out the ones who were hitting the demo button instead of doing their work. My classroom was noisy and chaotic, and I loved it.

Read More »

Me and my autism

I have been thinking a lot lately about identifying as autistic, and why – especially as a person who thought I knew quite a bit about autism – it took me so long to realise that I have it myself. There are still a lot of misconceptions about what autism is and how it displays, particularly in females. When I was learning about autism in the late 90s, the lack of theory of mind was an essential part of diagnosis, and we were taught that autism is much less common in women, but much more severe. As I’ve been doing more recent research, I’ve found I don’t really identify with a lot of the prominent autistic female narratives that I’ve found in books or blogs. For this reason I’ve decided to explore this in a series of short blogs as I get a chance to put my thoughts down, partly as a way of making sense of it myself, and partly for any other women who feel different but don’t quite know why.

Read More »