Newbie T1

Status
Not open for further replies.

AnchorFaced

Member
Relationship to Diabetes
Type 1
Hi all,

Have been meaning to introduce myself for a while and think now is as good a time as any.

I was diagnosed back in March 2021 after ignoring/not realising symptoms over the preceding 6 months. Having not put all the pieces together I just thought it was stress and would resolve after sorting out a challenging period at work. Nope.

I've always been able to put away food without putting on the pounds (Lucky me) however it became obvious that I was really eating a lot. Large bowls of Pasta, plenty of Mash, thanks, and generally a good diet but then I really started craving sweet stuff. A few more KitKats and Twirls in the fridge to raid on. All washed down with nice cold water...lots of water... and peeing. Curiously Breakfast was never my bag, I'd just load up on Coffee and have a snack around 10ish. I'm now eating large bowls of Granola everyday. Looking back I'm rightly mortified now knowing what was happening to my body. Did not have a clue. Eating what I wanted and losing weight (now down 10kgs at this point), sounds like a win.

Then I noticed the nervous shaky feeling dialled up a notch, always feeling stressed. I couldn't concentrate at work at all and tired most of the time. I do enjoy a cheeky nap on a Friday afternoon, always have done but this was up to every other day. Also I started feeling the cold and not the Bed warming champion of the previous years straight. My lower legs were cold, feet were blocks of ice, but it's winter and I live in a Barn. Still didn't really click and neither did my wife.

So by now I'm not coping at work. Falling behind in time sensitive assignments and not really performing to any great standard but at this point I also stopped caring, I just wanted to see the day out and have a nap. Stressed much? Possibly, because I've now a mountain of work I'm behind on. Fortunately my team are professionals and crack on, they know what needs doing and I've my No2 to supervise and manage them, which he does marvellously.

Google "Thirsty all the time and peeing lots" Click.
Well that sounds like me, yup I check all those and the dodgy eyesight. But am I? Really? How has that happened? Environment, Stress, Virus apparently. I don't know and neither does the scientific community. Better ask a Doctor because they know stuff and I feel like a Zombie with a sweet tooth.

I fire off an eConsult with my symptoms. Peeing lots, thirsty, will turn tricks for a Caramel. Click. Ring 999. Oh come on, I'm not that bad and love watching Channel 5 ER fly on the wall, so that's my benchmark for needing the Blues and Twos. I'll just ring for an appointment and so I get one for a week later. Sorted.

GP rings me on the weekend at about 0930 and asks if I can come in. I rock up and they measure my BG after I reel off my aliments. I'd not had brekkie that morning so my fasting BG tested 15 mmol (just a number isn't it). It wasn't long before lunch I was in Treliske to be seen by the Acute Diabetic team. I really hate (strong word I know) but I hate my blood being drawn. Can't help it. I tense up, breathing goes rapid and mouth goes dry whilst simultaneously receiving a Bafta and 2 Golden Globes for drama. And that is the life for this newly minted T1D.

Fast forward to nearly a year later and the HbA1c has dropped from an initial 114, then to 55 and now to 44 in November. My wife and I have grasped the basics, still reading and adapting to the fickle Honeymoon period which started around July with constant lows and coincided with being eligible for the Libre. My first meal taking no Bolus was emotional to the point of making a grown man cry.

Now we're both in a good routine, looking at the trends with my 1 unit of Basel onboard and roughly 1:10 Bolus for meals.

The NHS support has been amazing and my DSN has been on the ball with spot on advice and experience. Quite how she manages it with the workload and replies to my emails well out of hours. I feel fortunate for that, and the massive advances in medical devices where we are now.

My TiR is consistently over 90%, not worrying about the occasional high which always comes down with my last Beta cells squeezing a drip out conveniently to allow a cheeky snack before bed time.

It won't last and at some point in the unknown future I'll take on the full role. In the mean time I have my Libre to entertain, alerting us with false lows and random numbers but generally doing a decent job on the whole. I've learnt to spot carbs at 50 yards and can confidently enjoy a few miles walking without dipping and more importantly being able to do something about it if it does. Snacks, sweets strategically staged in the car, pockets, bags, bedside and the portable stab station everywhere I go. It's easy but constant work. I get good days where my range doesn't shift and I almost feel I'm not T1 but after a few emotional trips at the start, I'm not so easily fooled. T1 has me, not the other way round.

I've missed out loads but just an introduction right? Oh, I'm now 47, so a bit late to the party. Never know what you'll get and this spin of the wheel has kept life spicy.
 
Welcome to the forum
 
Good morning @AnchorFaced and welcome to the forum.

You made me chuckle over breakfast with your upbeat account of your journey through your diagnosis. Good to have you on here and I look forward to your contributions to the forum. The Honeymoon Period is an ‘interesting time‘ as the few remaining beta cells join in, sometimes. But it keeps you on your toes and having the Libre makes life a lot easier to head off highs and lows.

Keep in touch and fire away with any questions that arise.
 
Hi and welcome from another late starter. I am just coming up to my 3 year diaversary next month. All I can say is that it slowly gets easier, but it sounds like you are doing great already. I love bolus free meals but sadly they don't happen too often these days.
Which insulins have they started you on? Only 1 unit of basal is impressive!!

Anyway, good to have you on the forum and I hope you find it as hugely beneficial as I have. Please feel free to ask anything that you don't understand and if you fancy joining a slightly more social thread, come and join us on the "Group 7-day Waking Average" thread, The "Average" part has fallen by the wayside and we currently treat it as a virtual drop in centre where we post our waking reading and generally have a bit of chat about life, the universe and all that, diabetes related or otherwise.... I've posted a link below if you are interested.
 
Hi AnchorFaced, welcome to the forum.

Glad that you’ve been able to jump right into managing your diabetic journey. It sounds as though you’ve got a good grip of things so congratulations on your progress so far.

Do let us know if there’s anything we can do to help and do keep us posted on how you’re getting on.
 
Welcome to the forum!
I hate my blood being drawn. Can't help it. I tense up, breathing goes rapid and mouth goes dry whilst simultaneously receiving a Bafta and 2 Golden Globes for drama.
Oh, I felt the same way. Imagine when I first met my Diabetes team, I had blood taken, was trying to relax in the waiting room and the nurse came back like "I am so sorry, they just told me we need another sample" 😱 . I used to hate needles, so I also had a very dramatic moment when I heard I needed to start on insulin. But after 3 (or 4) blood tests in a couple of weeks, I don't feel too nervous anymore. At least that's a positive!

I love that you take it with good humor, take care and keep posting 🙂
 
Thank you for all your lovely replies and I do intend to keep posting as this a fantastic resource and helpful community. Having read many posts with great advice, either confirming what I was doing or enabling me to ask the right questions has been invaluable. I've my own newbie horror stories and will regale you all in other threads.
Which insulins have they started you on? Only 1 unit of basal is impressive!!
Started on Abasaglar and Novorapid and still using those. The Pens are great and switched over to the half unit NovoPen Echo for my Bolus.

When the Honeymoon kicked in, I did ask my DSN if the Basel could be stopped but she advised it was better to have at least some onboard.
I used to hate needles, so I also had a very dramatic moment when I heard I needed to start on insulin.
The drawing of blood from the arm is the exception. I can take Vaccinations, Dental numbing and the daily stabbing without a second thought, or Ricky Gervais announcing my name.
The Honeymoon Period is an ‘interesting time‘ as the few remaining beta cells join in, sometimes.
It initially was the most emotional period and from my experience the hardest to prepare for. I
 
Hello and welcome @AnchorFaced , glad you’ve joined us 🙂

Sorry you’ve had to join the diabetes club but thanks for a great introduction 🙂

Good to hear you’ve got Libre to give you an overview of what’s going on whilst your beta cells squeeze out their remaining insulin units :(

I can remember my honeymoon period in 1978-79 when I genuinely thought I was the first Type 1 to be cured. Sadly it didn’t last long!
 
Glad to hear that you have the half unit pens @AnchorFaced , especially in the early days as doses can be tiny, and the smaller adjustments make life so much easier.

I think for all of us it is a such a shock being diagnosed and I knew absolutely nothing about Diabetes at that time. However the learning curve was very steep, and the initial period somewhat unpredictable, and even now 14 years in there are days when my Diabetes just doesn't behave, and there is no obvious reason for the weirdness. Just one of those days.

The vast experience that is available on here is such a good resource, so whilst no one wants need to join, it is a great place to be able to share ideas, have a moan, ask for help, ….
 
Status
Not open for further replies.
Back
Top