Thank you so much for reading this blog. I do appreciate your visit and your support. As you might know, I LOVE COFFEE! So I've teamed up with a thing called Buy Me A Coffee. If you enjoy my content and appreciate the time it takes to create such things then you can buy me a coffee! If you leave your Twitter @ name when you buy me a coffee, I will personally thank you. If you'd rather be anonymous then that's totally cool. Thanks for the caffeine!
Thursday, July 1, 2021
Death & Taxes
Thank you so much for reading this blog. I do appreciate your visit and your support. As you might know, I LOVE COFFEE! So I've teamed up with a thing called Buy Me A Coffee. If you enjoy my content and appreciate the time it takes to create such things then you can buy me a coffee! If you leave your Twitter @ name when you buy me a coffee, I will personally thank you. If you'd rather be anonymous then that's totally cool. Thanks for the caffeine!
Thursday, June 24, 2021
Confessions Of A Diabetic
Please forgive me Diabetes for I have sinned against you. Have you ever been to a confessional? I haven't and I suspect if I did it might be a case of "Are you sitting comfortably? Then I'll begin!"
T1D comes with advice from the professionals for living healthily and rightly so! Once upon a time, that advice came in the form of strict rules. "You will eat at X O'clock, inject at X O'clock, wake up when we tell you to and pee in a very small tube for us four times a year". Things have improved, of course, and now I only need to pee in a very small tube twice a year.
With rules, comes rule breaking or maybe rule bending. And so, today, I present to you some stories of my own rule breaking and bending for your consideration. They are all going to be Diabetes related, of course and all suitable for family viewing although I encourage you, reader to not copy any of the below or think that because that bloke from the Internet got away with it then you will too. Are we clear? Super! Let's begin.
My rule breaking began at an early stage. Oh, lancets were being changed, carbs counted and injections given on time (at that stage) but at school things went very differently. Please check out Hobnobs in Hiding for some tales of my schooldays with T1D.
Following education, with a job, money in my pocket and a Fiesta Popular Plus on the the drive, the world was my oyster! Diabetes had to tag along despite me generally ignoring it and refusing to answer it's calls. Those were the days of parties, drinking, pubs, clubs, girlfriends and things were great! Of course they were. I think most people refer to their late teens and early twenties as great times. I'm no exception although I do feel incredibly lucky.
Shall we begin with hypos? I once made a video which described my worst ever hypo and it's still true to this day. Following a weekend of excess, I woke for work, showered, injected (twice per day mixed insulin jabs at this point), jumped into my car and headed off to work, no finger prick. I didn't need to take finger pricks, I hadn't for years at that stage, I could feel when I was low. Yeah, right! Yawning, tired, a bit hazy? Absolutely, it'd been a long weekend and I was looking forward to getting to work for a rest. However, yawning, tired and hazy are also strong hypo symptoms for me. Then the sweating began and I opened a window. Then the shaking... the shaking... oh no! I'm hypo. I grabbed my bag (still driving at this stage) and opened juice box after juice box. Because of my ignorance of T1D and the frequent hypos that I was coping with, I used to carry several with me in the car to take to work. I was probably 5 minutes from my place of work when the flashing lights began. I'd stopped the car and took it out of gear. Engine still running, I reached for what must've been my third or four juice box and then nothing. Black. I woke up in hospital, tried to punch a doctor and then started crying.
I'm lucky because I'd stopped my car in a busy place where police would often drive by. One spotted me with smoke bellowing from my car's exhaust. At that stage I was having a seizure and had planted my foot on the accelerator. There were seconds between that happening and me stopping the car, even fewer seconds between that and me taking the car out of gear. The police officer dragged me from the car, ripping my blood soaked shirt open in the process. I don't know if he was expecting to perform CPR or was just clumsy. Blood soaked? Oh, yes, I had bitten my tongue during the seizure and things got a little red for that lovely white shirt. I'm lucky. I spent the next week at home, recovering from that incident which could've quite easily killed me or many innocent others. Diabetes, on that occasion, had had enough of being ignored. My behaviour changed, I began testing my BG before driving and ate a breakfast. I took all my Diabetes stuff to work and confessed my condition to my incredibly kind and understanding boss, who hadn't seen or heard from me in a week.
Hypers were more frequent... I think! That's because, as you've just read, I wasn't taking any finger pricks. I don't remember getting any test strips or lancets on a prescription for several years! I wonder if my GP thought that I was cured? I was getting my insulin pens and needles and that was it. Remarkably, I was never unwell because of high blood glucose, no DKA, no frequent need for the toilet or raging thirsts. I would love to see my BG results from those days but suspect they would reflect my extremely infrequent HbA1c tests which were often around 9 - 10%.
How many HbA1c tests did I submit to? After passing out, following one when I was 11 years old, I have memories of three others over the course of the next decade. I didn't have time for blood draws and the ensuing bollocking from my then DSN. I was young! I was a roarer! a rogerer! a gorger and a puker! (You'll understand that if you've ever watched Blackadder).
My DSN gave up trying to convince me to have an A1c. Instead, she relied on my detailed blood glucose diaries. Never in the course of human history had so many lies been written in one book, it was like a Tory manifesto! Of course, she couldn't question why I was always between 4mmol and 8mmol, solidly for a month because I wasn't letting them take an A1c from me! Those works of fiction kept me in their good books for years. Little wonder that I gained some success as a poker player in later life.
"How was your appointment?" family would sometimes ask. Oh, you know, fine considering I hadn't been and was eating a bacon sandwich in the Cafe instead. Nothing tastes as a good as a bacon sandwich when you should be getting strips torn off you by an angry DSN. Yum!
Life changes. I grew up, kind of, eventually and with family comes greater responsibility. Today, I check my BG all the time! I wear a CGM and finger prick to calibrate it. I go to my appointments. I don't lie to my HCPs. My A1c is between 6 and 7% and I will submit to as many blood draws as I'm asked for.
My blog is for my thoughts and brief tales relating to Diabetes. I have a larger collection of notes and stories which aren't necessarily family friendly. Confessions Uncut, if you will, which might make an interesting book. Should I write it?
In the meantime, if you relate or have a confession then tell me everything, my child in the comments below or Tweet me!
Thank you so much for reading this blog. I do appreciate your visit and your support. As you might know, I LOVE COFFEE! So I've teamed up with a thing called Buy Me A Coffee. If you enjoy my content and appreciate the time it takes to create such things then you can buy me a coffee! If you leave your Twitter @ name when you buy me a coffee, I will personally thank you. If you'd rather be anonymous then that's totally cool. Thanks for the caffeine!
Thursday, June 17, 2021
Diabetic Oddity
Major Tom/Bowie went on to describe leaving his space capsule and entering the void of space. Bowie was a tremendous lyricist and wordsmith, of course but I wonder if he would've considered a hypo as "floating in a most peculiar way"?
Perhaps he would've come up with a description which is beyond most of us.
Where am I going with this blog? I've made comments about this previously. That the words we use to describe Diabetes, our Diabetes, cannot ever be challenged. I describe myself as a Diabetic or a Type 1 Diabetic. I take blood tests. I try to control my Diabetes.... Oh! Ground Control! Perhaps I'll stop trying to ignore Bowie in this blog and just carry on referring to his lyrics.
Control is an interesting one. It seems to bring about great angst from some while others use it freely. Myself, I'll use that or "management". There are two reasons for that. Firstly, I'm of a vintage that is not upset by the words used by others unless they are used with the intent to cause upset or are used through hate. Secondly, sometimes, elements of MY Diabetes can be controlled. If an HCP asks me "How is your control?" or "How is your blood sugar control?" my first thought isn't how dare you use 'control' for a condition which isn't controllable! I'm not going to stand up and walk out or aggressively correct them. Instead, my default thought is that they're trying to get a basic grip on how I'm managing, lately. Lots of hypos, hypers, 100% in target, everything in between... something that can be improved? Great! If not, we move on to how magnificent I am. I accept "managing" and "control" in the same way.
I firmly believe that we shouldn't be challenging singular words in such circumstances. Reviews or appointments can be stressful occasions for us, as patients. I think our focus should be on gaining a positive from that 10-15 minute time slot and not leaving the clinic, feeling unnecessarily tense. HCPs are advised and trained on how to interact with patients but they're human beings. Human beings make mistakes sometimes especially after years of using some words which are now considered "No-Nos".
That doesn't mean we should ignore or forgive absolutely everything. I think if your HCP insults you or puts you down, if you're made to feel like a naughty schoolchild, then that's absolutely the right time to be vocal and complain.
What is correct and not correct in regards to how HCPs interact with us is personal to you. Your own offence is completely valid, of course. I do think it's time that we stopped indicating what is right or wrong, in regards to language, to people living with Diabetes, though. There is no right or wrong. You don't need to change the words which you've been using forever when talking about your own condition. We have enough on our plates, in my opinion. Leave the "correct" way to talk about Diabetes to your overworked and exhausted HCPs. Overworked and exhausted after working in hotbeds of Covid-19 for 18 months - Perhaps something to consider when the next HCP puts a foot wrong.
One thing which I do struggle to control is my coffee addiction...
Thank you so much for reading this blog. I do appreciate your visit and your support. As you might know, I LOVE COFFEE! So I've teamed up with a thing called Buy Me A Coffee. If you enjoy my content and appreciate the time it takes to create such things then you can buy me a coffee! If you leave your Twitter @ name when you buy me a coffee, I will personally thank you. If you'd rather be anonymous then that's totally cool. Thanks for the caffeine!
Friday, June 11, 2021
It's Good To Talk
Saturday, May 29, 2021
Incomparable - Oh, We Are Not The Same
Friday, May 21, 2021
What a Site! - Diabetes Tech Worn by Everyday Diabetics
That's Julie, she says "I wear my sensor on the side or to the front of my arm, because I can see it I’m more conscious of it so I don’t knock it off, when I wore it on the back of my arm I was always knocking it off especially at work and when strength training."
Jimmy likes to keep his sensor warm, "I wear my taped up sensor on the inside of my arm (it doesn't like the cold)"
Some sensors have a habit of coming loose and falling off! So putting a strap on could be a great idea, especially if you have a 3rd party add-on such as Bubble.
A late entry comes from this patch pump user. What goes on around the front, goes on around the back.