We have to do a third levemir shot at 1.30am for my daughter to help stop the morning rise. Prior to this we were giving novorapid at 5am so she didn't have a rapid morning rise. We're normally up several other times a night sorting her blood sugars anyway!
Hi donnelysdogs, I've had a few switches of insulin regimen over the yeard but for the last 16 years I've injected in early mornings to beat the dawn phenomenon, it's been my own trial and error, and my current regimen is:He done late shifts for a very long time... so when diabetes should fit in to our lives I dont particularly want to go to bed without him and then just be disturbed anyway... so the worst part is 4am waking and then sometimes brain just is not awake and functioning or it wakes and I'm then awake... if I want to get up because I'm awake then I have to inject... and then if I found myself tired I couldnt go back to bed cos I've taken my waking dose as well and will go hypo.
So total frustration. When mornings are dark the livht has to go on to inject so hubby disturbed as well.
Just wish there was an alternative to the 4am waking or just to hear that somebody else has to do it would be good!! If you know what I mean..
I know on pump my basal rate shot up from .33 before 4am to 1.25 starting 4am and the cgm confirms I have to do it.
Hi donnelysdogs, I've had a few switches of insulin regimen over the yeard but for the last 16 years I've injected in early mornings to beat the dawn phenomenon, it's been my own trial and error, and my current regimen is:
- 5 a.m Levemir
- 6 a.m Novorapid 1 unit (with put food, so by 8 a.m I'm usually between 4.8 - 5.6).
- 7 p.m Novorapid 3 units with 10g carb two thirds protein, including a big salad.
- 4 p.m 2 units sometimes without food, usually with 10g carb, like an apple.
- 9 p.m Levemir
I sleep early and wake up early, I'm working by 8 a.m. and if I don't inject the Novorapid in the morning, without food, my BS would go up to 13 or more. It took a while to adjust it to a steady level but I found that in the mornings my BS tends towards highs so I cut out eating my apple, (I've never been a breakfast eater really) then and it would stay level until lunch time.
20 or 25 years ago I injected higher doses and ate more varied foods but my metabolism changed and it's down to the same amount of the same thing each day now. Boring as hell but I'd rather avoid the mess of spikes and stick to the same meals, if you can call them that.
So you're not the only one doing early morning shots, and I know it's a pain, but I wake up a few times between 2 a.m. and 4 a.m. and sometimes inject 1 unit of Novorapid to correct an upward-looking result. I test 8 or 9 times a day, if not I wouldn't have a clue.
43 years of this cruel T1 hasn't made it easier, I certainly don't have great control of B.S all the time, I do a lot of corrective shots. Sometimes the body just wants to do its own thing and I tear my hair out. Thankfully I haven't had to buy a wig yet.
For me T1 is draining, all the testing and planning and intervention when necessary. But it's there and we have to bite the bullet, to get on with it...I tell myself to take it one day at a time. No more beating myself up like I used to; that only came when I realised and accepted there's no such thing as perfect control which clinic visits always made me think I wasn't getting and had to strive for. My control is not high or low, it's in between, I make a lot of effort to be 'stable' and it isn't easy.
I'm sure maby of us would relax a bit more if some doctors and nurses who falsely believe there's an ideal perfect diabetic control stop adding to the burden of diabetes with that attitude. There's always a cloud of censorship about how good we are at controlling those bloody BS and how doomed we are if we don't get it right. If we were conditioned to relax about our results -yes work on getting better results - but relax and not be under that horrible gun, it wouldn't drain the living daylights out of us so much, that head pressure to get it right all the time. They should try living with it for a day.
I must shut up now. Hope you're feeling alright.
@donnellysdogs , the 1.30am levemir isn't perfect...1 unit drops her a bit much at 4am and half a unit still gives a small morning rise, but it helps a lot. It's never perfect is it?! But we're having the best nights we've had in the last 2 years. We've discussed pumps with our team, as they're keen for my daughter to have one. We're reluctant to go for it just yet though as she's doing well with MDI and dexcom at the moment and we worry about her losing her sense of freedom being attached to something else.
What about the omnipod? It is a wireless pump! Not as accurate as the 640g or as 670g will be but far more accurate than mdi! I'm going on the 640g but I have looked into the omnipod too! It has a hand set the size of a mobile phone and the reservoir is in the pump which attaches to ur delivery site!I used to but after 5 years brilliant use I cant tolerate cannulas and them blocking. Not just occasionally. The hosp mentioned me having the 670 with sensor when its available in UK but after I asked how the cannula problem could be overcome they agreed basically that the algorythims of the insulin and glucose wouldnt be able to cope. So MDI is only option.
What about the omnipod? It is a wireless pump! Not as accurate as the 640g or as 670g will be but far more accurate than mdi! I'm going on the 640g but I have looked into the omnipod too! It has a hand set the size of a mobile phone and the reservoir is in the pump which attaches to ur delivery site!
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