Because I am hyper-organised (crap), I scheduled time to write a post for World Diabetes Day—spot the deliberate mistake. Said designated day took place on 14 November, unmarked by we at the Diabetes Diet. Hey ho!
Instead, here I am posting about it more than a week later. You could argue that living with diabetes also takes place on the other 363 days (and the extra one every four years) of the year, so why make the 14th special, although awareness-raising exercises are always useful.
Anyway, I thought I’d list some of the quirky things about living with diabetes. We all know the big stuff, but there are some teeny-tiny bits you put up with which aren’t obvious to those who don’t have the condition…
Gnawing anxiety when parted from your bag. I have an industrial-sized handbag so I can carry around everything—blood testing equipment, two pens, spare needles, jelly babies and a full make-up kit*. When I visit people and they try to take my bag from me to put it with coats, I cling to it. I’m never more than a few metres from that bag.
A trail of litter that follows you everywhere. I do my best to dispose of it at the time, but I wish someone would invent a small bin that magically appears at your side every time you do a blood test or injection so you can throw away your used needles and blood testing sticks there and then. Every few days or so, I have to do a clear out of my bag where old needles, their wrapping and used sticks gather at the bottom. Once, I was in Regent’s Park in London and I spotted a used blood testing stick on the group and it delighted me. I knew it wasn’t mine**, but the thought that there was another type 1 in the vicinity felt comforting.
An aversion to ordering drinks when you are out that are in a glass. How do you know it’s the diet version? I only feel secure when my drink comes in its bottle or can. Otherwise, you might end up drinking the full-sugar one which will hit you like a sledge hammer almost immediately.
Puncture-marked fingers. I’m still on the waiting list for the FreeStyle Libre so in the meantime, my fingers keep that little collection of black dots that marks frequent finger pricking. You are supposed to vary the fingers, but my right hand bears the brunt of tests because I’m left-handed.
Toilets are very important. High blood sugars make you pee a lot and the first thing I work out whenever I go anywhere is—where’s the loo? Also, I’m not fussy. I have friends who won’t use dirty toilets such as the ones you get on trains. I don’t care. It’s a loo and it’s going to take me from bursting discomfort to huge relief in minutes.
It’s a full-time job. Managing diabetes takes up a lot of time and energy. You don’t get holidays and you can’t quit, and you have to do it on top of everything else you do. The boss is often a moody cow too. The skill-sets needed include arithmetic (figuring out insulin doses to match food), organisation (making sure you have everything you need when going out and keeping on top of your prescriptions), an understanding of biology and how your body works, and the ability to forward plan for most aspects of your life.
*Strictly speaking, not needed for diabetes
**On second thoughts, it could have been. Those things get everywhere. I’m always finding them in weird places.
It sounds like a real lifestyle! But you look like your handling it like an expert. Xx
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Thanks Sharon. And there are far worse conditions to have than type 1 diabetes. Plus the ‘job’ skills you get from it are transferable!
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I enjoyed your post Sharon. It truly is a full time job. One thing I do is to eat at the same time everyday to help keep my glucose numbers regular. Going out to eat off schedule messes me up.
Teri Green
Atlas Biomechanics
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Yes, you have to find what works for you.
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I’m just back from holiday. I went a snorkelling trip with Steven. One hour in the water. There was a cliff side on the water’s edge so there was no opportunity to stop once started. He overdosed on fanta full sugar before hand to make sure he didn’t have a hypo. There is a lot you take for granted when you don’t have insulin dependent diabetes.
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In Australia, we have a government funded toilet map. It’s more for people like me with an irritatable bowel, but it works just as well for people who need to empty their bladders often too.
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Amazing! I’ve been known to use toilets in council buildings on the lines of my council tax paid for this, so I’m entitled to take advantage.
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I’d say go for it. Better in a toilet than not.
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Don’t forget having to eat jelly babies to be legally allowed to drive 😬
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I keep hoping they’ll start doing packets of black jelly babies only. Or making them free for diabetics.
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my doctor says he can tell who tests and who does and does not test regularly by the marks on their fingers. Yeah mine have the tiny black dots all over them.
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It once turned up in a crime drama on the BBC where the pathologist could tell the dead body in front of her was someone with diabetes, thanks to the black marks!
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Exceptional Article
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