Hi Gerri – thanks again. I’m trying to make sense of this but as I’m very, very, VERY visual, it’s hard to comprehend or communicate what’s going on without us both looking at my beloved white board. ;0) I really am trying – and I really do appreciate your helpful advise more than you can probably realize. I wish you were my doctor! ;0)
Let’s say I split my Lantus dose and take 20 IU at 10 p.m. and 20 IU after I get up, say at 8 a.m. Won’t I end up with MORE Lantus in the evening (between 10 p.m. and midnight) when I don’t need it – and LESS Lantus in the morning (between 6 and 8 a.m.) when I do need it?
Given the advertised (?reliable?) coverage of 24 hours “life” from each injection site: I’m visualizing these doses as being stacking during their full-coverage times, and each one causing the stacked totals to taper off in little dips two hours before each injection and then ramp back up at the time of the injection. Do you see what I mean?
Granted the dips and rises will have less amplitude with two injections, but unless I set the alarm and inject one of them at 3 a.m. (rather than in the evening) it seems that the dips and peaks will hit exactly when I don’t need them to hit. ???
I am working on collecting data to get my insulin:carb ratio and my IISF (thank you!!!) and I agree that the doctor’s sliding scale is way innacurate and cludgy.
I know I need to increase the Novolog (most in the morning, less at midday, least at night) but in the meantime, it seems like I have a big Lantus problem, too. I can only increase it so much without going frequently hypo between say 11 p.m. and 3 a.m. or whenever my darn Dawn Phenom rears its head. I’ve already had one severe hypo at midnight and another at about 1:30 a.m. I can’t track my blood sugar all night manually AND sleep.
What I WANT is CGM and I’m putting all this into charts and spreadsheets to try to convince the head of the diabetes program at my HMO to get off his duff and help me get CGM approved by the HMO. I don’t give a rip what 80 of their Type II patients need or don’t need. I’m not in the 80%. I’m me and I have genetics that are unique – Chippewa, Choctaw, French, German, Serbian, English, etc. tons of auto-immune disease in my family, a genetic complete lack of a diurnal cycle in everyone descended from my Great-Grandmother Emma (it’s called a free-running circadian rhythm), etc.
My HMO has this whole song and dance about “our studies show that CGM doesn’t make a measureable difference in type II outcomes over time” and I just want to SCREAM at them, “Then what is your FREAKING plan to help ME?”
(Insert sound of head pounding here.)
I told my doctor I’d be willing to pay cash for it, but would you believe our HMO doesn’t even have a soul on-staff who is qualified to train patients how to use it or monitor its use afterwards, so they won’t prescribe it? To me that sounds like malpractice but for some reason they’re getting away with it. I think their standards of “care” are bordering on criminal.