K
I'd revert back to the previous version.
Although, knowing my luck it still wouldn't work because I didn't clear everything out and then forget to eat because I was having too much "fun"debugging the Xbox.
Oxford and my garden are flat and flood so the walking around is easy for me, must be hard on a slope, good exercise thoughI remembered to take my rings off but my watch also keeps track of my activity and I didn't want to mis out on my steps up and down the garden. And when I say "up" I mean up as it is a steep garden.
Good luck!@hh1 I'm doing the heavy duty stuff this afternoon............ got 75 tulip bulbs to plant and all the leaves to bring together and dead heading and the list goes on. No long walk though so hope madam BG will behave................. unlikely!
I have the pump clinic next Tuesday to see if i may be a suitable candidate for one. Last week had a really good week, but as with all things type 1, overnight and this morning, its all gone wrong (or maybe right). I am deliberately not taking any additional correction doses.
So a decent day yesterday from midday to bedtime, staying around the 6.5 mark, which i am happy with. Bed on a 6.2, slight movement to 6.6 at 2.45am, before finally reaching 10.6 when i got up this morning. Welcome back dawn phenomenon.
Had my porridge plus correction does and 2 hours later sat at 13.9. Now just before lunch sitting at 10.4. I would have expected this to be around 6. So more correction dose with lunch and lets see how this goes.
I am also keeping a food and insulin diary for the next 9 days, give the consultant something to work with
I think that's the one thing I truly resent about T1 - having to eat sometimes when I really, really, really don't want to!Ive just tested b4 i go to bed and hypo again at 3.2 although i dont feel ill would illness make you have lower bgs normally im high if im not well im sat here with a piece of toast im not even hungry grrr
Hi @helensaramay, You raise a very pertinent question. And the wish to be super-independent is boon and a curse regarding this.
In early years, before glucose meters and better insulins, I was canoeing alone, hiking and doing 7 day canoe trips through wilderness terrain with relative strangers, and went tramping around New Zealand by myself at times.
At the now 52 year mark on insulin after one particularly bad hypo where i stopped breathing and my wife saved me ( some mouth to mouth resuscitation and 2 glucagon injections later) I cannot imagine being on my own.
That episode led to me being on an insulin pump and that has made a BIG difference but not enough to relish any thought of living alone. I have to agree with the notion that control of one's type 1 diabetes becomes more difficult the longer one has it but CGM in whatever form, pumps etc have changed the diabetes landscape for TIDs so much in recent years that there are better chances of being independent for longer is my guess.
So how did after lunch go, well not that great. Just about to drive home at 4pm and its dropped down to 4.5, so cup of coffee 2 sugars and a biscuit and within 5 minutes its up to 5.9. Drive home it now 8.4, an hour later its dropped backed down to 5.9 and falling.
One thing predictable about type 1, is the unpredictable
Totally agree.What a wonderful post.
I have to agree how the hell did those of us with type 1 for 30+ years actually survive 1970-1990 when we had no blood test meters, all we had was pee on a stick which was useless
Now we have blood meters, cgm, better insulins, insulin pumps. Where are we going to be in the next 30 years
Hi @helensaramay, You raise a very pertinent question. And the wish to be super-independent is boon and a curse regarding this.
In early years, before glucose meters and better insulins, I was canoeing alone, hiking and doing 7 day canoe trips through wilderness terrain with relative strangers, and went tramping around New Zealand by myself at times.
At the now 52 year mark on insulin after one particularly bad hypo where i stopped breathing and my wife saved me ( some mouth to mouth resuscitation and 2 glucagon injections later) I cannot imagine being on my own.
That episode led to me being on an insulin pump and that has made a BIG difference but not enough to relish any thought of living alone. I have to agree with the notion that control of one's type 1 diabetes becomes more difficult the longer one has it but CGM in whatever form, pumps etc have changed the diabetes landscape for TIDs so much in recent years that there are better chances of being independent for longer is my guess.
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