Type 1'stars R Us

Hehe I forget about that aspect Never knew how much insulin had gone in!! Just reattach and push the plunger and hope for the best

 

@porl69, another hats off, these make me want to hide behind the sofa
Off for my 2nd scan in a month. I've got to drink 2 pints of water an hour before. Sorry forgot I wouldn't mention numbers and these aren't that important anyway

 

Lol, I learned not to ram it home too fast. Nice steady action. Problem was with the glass syringes occasionally there was a little resistance with the plunger encountered in the glass syringe barrel which needed a little extra exertion, breaking the steady flow & "bottle necking" the needle?

With leg injecting rotation, I had this diagram with days of the week. Alittle like a butcher's cut, wall hanging or miniature car parking spaces mapped out on both legs...

 

Hello everyone!! Hope you all had a great new year and Christmas!

I have a quick question, I’m trying to do a low carb diet, (yes another new year resolution!) not for weight loss but just to try and improve my health in general, but obviously it’s quite difficult to do a really low-carb diet without having hypos at the start? What type of foods do you eat when you’re having a hypo but trying to avoid carbs?!? Currently I’m drinking Lucozade which seems to be working but thinking I might grow tired of that and it goes flat if you open a bottle and then don’t use it for another few days!

Any ideas would be most appreciated!!

 

eek!

 

Hi,

Firstly? Basal test. Whatever the amount of carbs or not in a diet you bolus for, get the groundwork sorted first before the building.
https://mysugr.com/basal-rate-testing/

Secondly, don't avoid carbs if you are low. A couple of Jelly babies or the same number from a more covienient pack of fruit pastels do it for me..
Insulin is a ride you can't get off. So if it goes adrift? Don't feel you failed at LC. Treat that hypo.

Edit, I'll tag in @Mel dCP she's a recent pumper & LCs.

 

I would suggest Glucotabs - you can have a measured amount to quickly bring you out of a hypo and they don't 'go off' quickly. You're also unlikely to be tempted to neck the whole tube of them.

@Jaylee makes a great suggestion to do some basal testing - as it's perfectly possible this and your ratios will change as you adapt to a new diet.

 

I was DX'd in 1997, so missed the torture tools and chemistry sets, but did use plastic syringes, 12mm needles, and drawing up from vials of insulin, and very early on pee dip strips and matching the colour on the side of the pot. I can't remember my first proper blood meter but I know it seemed to require a lot of blood. I can't remember ever being told about CP, or anything else really - it was start at this dose eat that amount, speak to the nurse and we'll adjust the dose as and when. But I do remember that first dose of insulin was like a magic bullet. But the steel needles look horrendous - physically and psychologically life scarring!

How many of us will be dreaming tonight about 12 ft needles chasing us around an impossible maze of Mars bars (fun sized ones at that)!

 

20 years for me, and I think the same re the torture age. I was put on MDI, given novopens and a medisense meter (possibly with a small cost) - test strips on the NHS, needles weren't for a while. The stab-u-like device wasn't a horror. I was also given a vial of each insulin and a handful of syringes - I still have the syringes They didn't try anything with exchange units or carb counting at all. I remember asking the consultant when diagnosed what to do with different readings (since it was obvious to me that I could use them as a guide to tweak things) and he dismissed me saying I should treat them as random! I worked it out for myself...

 

When I lived in Leeds, around 2001-2002, I was being taught carb counting for the first time under the team at LGI, as I had just made it onto the pump waiting list. Alas, I didn't get the pump (as I was moving away), but I adjusted my MDI doses accordingly, and loved the flexibility. When I saw my suburban GP for something unrelated, about a year later, he tried to convince me that I should not be carb counting, nor should I be varying my doses. Seems he was of the old school where fixed doses and constant snacking to balance the insulin were the norm. I politely nodded and ignored his advice...

 

Ooooops.....apologies to you. There are worst implements BUT there maybe be youngsters on here and we dont want them to have nightmares . Ewwww fake orange taste is the pits, they would have been spat out,,,,,,,conference call or not lol

 

Not strictly low carb, but if I can catch a low early enough, I try an apple, orange or banana. I figure it is a good opportunity to get some fruit onboard. I think you have to go a little bit easy on yourself while you adjust your insulin to your new regime.

 

Oh this thread make me giggle

All this trip down memory lane is fun.

BUT hindsight is a wonderful thing. Yes syringes, needles and testing kits were interesting and fun to use some 20+ years ago, BUT at the time that was all that was available and it was simple a case of use or...…..well I like life and cake...….

Things have moved on, all for the better, but they do with all aspects of medicine and treatments and dealing with long term conditions has improved greatly over the years no matter how bad your GP/DSN/Medical Team may seem to you. Plus it will only improve as we move forward in time.

I get the whole "glad I was not diagnosed when I was younger...……" where as I am the opposite, I really do admire people who in the later years get this wonderful condition we enjoy and share because as I have seen it is a very BIG change in the way you live your life after diagnosis.

T1D is not rocket science, yes, I get the reason why people are scared of it and fearful of it.
But there are plenty of us out there that have had it for a very long time, before all the various diet fads, carb counting, MDI, pumps, fitness regimes, technology etc etc and some are walking wounded some are still intact with just flesh wounds but we are still here to offer (dubious ) advice and sometimes a realty check, plus a shoulder to cry on.

These days with the amount of information on offer plus the advances made in care, blood testing, nice lovely thin needles and variety of insulins it has never been easier to keep a track of this T1D malarkey and should NOT stop you from enjoying life (cake, chips, booze, rumpy pumpy, full fat anything) and stop you from doing anything.

Having said that it at times, T1D does things I have no idea why, annoys me, frustrates me and many WTF moments however it does not stop me doing anything and tomorrow will ALWAYS be better.

OK that might upset the apple cart, not meant to but you might get my drift. As I said in the rant I sometime see thing in a different way to other.

 

Thank you for the replies, yes I only got the insulin pump back in September so still adjusting the basal rates, my biggest annoyance is at night! A few nights on the trot night my BS shoots up, so increase my basal to counteract or try a temp basal, the following night I’m hypoing! My control is rarely above 10 during the day but nights are a pain!! Think I need to invest in a Miaomiao!

I’ve seen a lot of people post about low-carb diets helping them so thought my New Years resolution could be to give it a go, but do tend to have hypos quite regularly...I do like jelly babies!

As much as I could do with losing some weight due to other relating health conditions (Addison’s Disease), I’m fed up of feeling rubbish so feel it’s worth a shot!

Been diabetic 24 years (since 8 months old) so you would think I’d be a pro at this by now but still learning everyday!

 

Was it basically a colour -> number converter?

 

Good afternoon just a quick pop in to see if your all behaving lol


Had a drive into bandit country this morning and escape unscathed

 

@Knikki here here! with you all the way.

So we've looked back at the past and shuddered at the archaic devices and protocols some of us had to endure, do you think in 20yrs time we'll be looking back and laughing at the fact we had to inject using 4mm ultra-thin pen needles, stick funny looking CGMs and clunky pumps to ourselves - what would you image would be de rigueur by then?

 

@Knikki, no apple carts upset here, love the let's just enjoy life approach - until the next WTF gets me

@Cumberland, where's bandit country?

@slip that's a fascinating thought. I don't think about what might be in the future as it sets up hope for a cure; I'd rather just get on with it, accept any improvements that come along, and maybe I'll get the great surprise one day!

 

I have mostly normal blood sugar levels, but sometimes it goes higher, just wondering if it is possible to follow a low carb diet, and reduce the insulin I take

 

I was just about to post the same thing. All this talk of heres what it was like 30 years ago, got me thinking how much things have improved in past 10 years or so.

The next question will be what will type 1 look like in 10/15 years time. Will we we look back in horror at the fact that we had to inject ourselves numerous times per day. The primitive finger prick testing we did maybe 10 times a day. The constant struggle with highs and lows.

Amazing progress has been made in past 10 years, with insulin pumps, CGM, even better insulins, long may the progress continue

 

Blimey, I missed a lot of torture instruments! I was diagnosed in 1998 so was straight onto pens, but I had to buy my own needles. As a student, having to pay £20 a box was beyond me, so I used to make mine last as long as possible. Blood testing took ages and the results were read from a colour chart on the tub!

Interesting shift today, an elderly gent with heart failure. I must be getting used to this, I’m not getting the massive adrenaline spikes every time we get an alert. Although this one came in just as I was pulling up my trousers after a toilet stop and made me jump!

I’ll try that, thank you! Got yoga tonight, but it’s a stretching and gentle class and doesn’t seem to affect things too badly.