Cheers. Ive been ok for a while and the diabetes has sort of eased off a little, even though its always in the back of my mind. Today has thrown me little but I feel ok now and last test over 2 hts ago i was 10.2 but i will be less now so happy ish days.3 and a half months then, sorry I was half a month out!
pre-diagnosis the pancreas is trying as hard as it can to produce insulin with x number of beta cells down, then along comes some extra injected insulin to ease it's burden, and in fact make the pancreas redundant as you're covering all the carbs off with the injected stuff - this gives it time to repair and recuperate a bit - so it eventually gets back working or at least trying to and coughing and spluttering insulin as and when it can, hence the lows and/or not needing injections to cover some meals.
But there is no way of knowing if and when your pancreas is going to play ball, so unfortunately lots of testing and hoping for the time being - you'll soon notice if and when it completely packs in. I think the honeymoon period is probably the hardest time for a T1D, you're probably still reeling from the diagnosis, and think you've got a handle on it and then wham lots of lows and then even the thought of the possibility that the docs got it wrong.........!
It will get easier, just keep testing and go careful.
Had to laugh at this one, sounds about right!I think Fridays shenanigans by my Pancreas had worn the little fella out, and on Saturday he decided to have a bit of a rest.
I test two hours after every meal bar breakfast as eating the same food was not having much of an effect on my sugars, so I decided to give my aching fingers a rest.As you are on so little insulin, if you don't have one already it might be worth asking your diabetes clinic for a half unit pen, then you could perhaps see if 0.5u with a meal might help with the rise - if that's happening most times, your #8 post seem to indicate you don't routinely test after a meal hence the query about going high after food?
Had to laugh at this one, sounds about right!
6 Weetabix sounds a good amount to start the day with. I used to put banana on mine.I love weetbix and have eaten them every day since I was diagnosed. I have found that they're a great food since they're fairly moderate GI, easy to carb count, filling and delicious! I've had 6 today alreadyI agree with everyone else - your experience sounds like a typical problem for newly diagnosed people. Just wanted to share my weetbix experiences!
6 Weetabix sounds a good amount to start the day with. I used to put banana on mine.
I could eat 6. Normally have 4 but that's rare at the moment.Not all at once lol! I had 2 for breakfast, 2 for lunch, another 1 for lunch coz I was still hungry, and 1 for afternoon snack. I put peanut butter on mineMy breakfast today was 2 weetbix, an apple, and some chocolate ice cream
I never have more than 3 at once. But sometimes I feel so hungry and I would love to eat 6!I could eat 6. Normally have 4 but that's rare at the moment.
When diagnosed, my brother a 35 year veteran turned up on my doorstep with a bunch of flowers and a box of Weetabix. Your new best friend he said.I love weetbix and have eaten them every day since I was diagnosed. I have found that they're a great food since they're fairly moderate GI, easy to carb count, filling and delicious! I've had 6 today alreadyI agree with everyone else - your experience sounds like a typical problem for newly diagnosed people. Just wanted to share my weetbix experiences!
One of the lads at work gave me a penguin biscuit and said 'I hope that doesn't kill you '
Have you had a look at a Freestyle Libre sensor? (your DSN may have some(1) to give out for a trial)so I decided to give my aching fingers a rest
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