Fears are funny things. I have a lot of them. I'm scared of spiders, clowns, roller coasters and flying. I'm the worst person to watch a horror movie with - I will almost definitely scream, and I will have nightmares. I'm scared of the fact I have no life plan at present and, not that I'll openly admit it all that often, I'm scared that I won't get my (happily-)ever-after. And not in a I-need-to-settle-down-right-now way, but more a will-I-even-let-myself-settle-down-with-someone.
But fears often change. Not all of them, but as we grow up and change as a person, our fears change too. When I was a kid, I was terrified of dogs. Looking back, I'm not sure why, but now I'm such a dog person! Sleeping in the dark used to scare me too. Heights were a no-no. And, somewhat ironically, I used to also be terrified of needles.
When I was diagnosed with diabetes, I was sent to A&E and on arrival I was given a bed and told that a nurse would be round to insert a cannula into my arm. And I was terrified. My Mum did her best to distract me, but I could not focus my mind on anything other than the horrible nurse putting a cannula in my arm. (I should say, he wasn't actually horrible at all -- he was just the one inserting the cannula, so by default I didn't like him). Throughout my hospital stay, I had many blood tests done, my fingers were pricked every two hours, and I had to have another cannula inserted too.
After three days of being on a sliding scale of insulin, a DSN came to see me and told me that I couldn't be discharged from the hospital until I could administer my own insulin injections. If there was ever going to be something that made me get over my fear of needles, that was it. I took the insulin pen from her, I screwed the needle onto it, I pinched the skin of my right thigh, and I did my first injection. I was desperate to go home.
After that, I can honestly say I haven't flinched at needles. The needles my insulin pen took got progressively smaller (8mm, 6mm, 5mm, 4mm), I went for my flu jab every year, I had my BCG jab earlier this year, and I moved onto an insulin pump where the cannulas I started out with were 6mm steel ones. No problem.
So, yesterday morning, why did I completely freeze up when I had to use this?
My brain would not let me press that little button on the side to insert this cannula, a FlexLink, one where the needle comes out after. It took me about half an hour to work up the courage to do it (as well as a text to Lizzie and Shep, and some encouragement from some wonderful people on Twitter).
It's funny how our fears manifest themselves. I'd seen other people use the LinkAssist. I knew how to use it. I'd even used it on one of the soft-toy-pumps at clinic (yes, my diabetes clinic has soft-toy-pumps...very weird at first, but now I kind of like it). But holding it against my hip to "fire" into my skin...fear took over. Very weird.
It's funny how our fears manifest themselves. I'd seen other people use the LinkAssist. I knew how to use it. I'd even used it on one of the soft-toy-pumps at clinic (yes, my diabetes clinic has soft-toy-pumps...very weird at first, but now I kind of like it). But holding it against my hip to "fire" into my skin...fear took over. Very weird.
On a lighter, and much funnier, note, the tubing that came with the cannula above is 80cm long. And I am a very short, clocking in a height of 5ft1" (and a half...the half is very important!)
It's safe to say I'm very much looking forward to my delivery of 30cm tubing!
It's safe to say I'm very much looking forward to my delivery of 30cm tubing!
I know what you mean about not pressing the 'fire' button, even now (7 years on pump) I have the odd day when I don't want to press it. Also, not sure if you know, but there are 60cm tubes if you find 30cm too short :) x
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