(For the record, I didn't realize how long this post would be. I apologize in advance.)
I hate asking this. I truly do. I've been torturing myself with this question for about two years, and I figure that if I can bring this up anywhere, it'll be here.
Am I better off just going on insulin and getting it over with?
I NEVER talk to people about this, but while on the phone with a friend tonight I admitted that I don't care if I'm put on insulin, because it truly doesn't scare me and anything is better than what I've been experiencing lately.
I know I just upped my dose of Met, but honestly I don't expect that to do much. The Met worked "well" originally, or maybe I was so happy with the way I was feeling that I didn't mind the actual numbers. Then it wasn't working so well, and I wasn't feeling so great anymore. So my endo told me to up the dose.
I don't like this runaround. My BG control has been getting progressively worse over the last three or so years, but this past year has been the worst.
I don't want to change things again and again and know I'll probably have to change them again. I don't think this is going to be a matter of changing the meds until we get it "right"--because, honestly, that hasn't been my experience. Januvia worked fine for the month and a half I was taking it, and then everything went to hell once I stopped. (And knowing what I know now about Januvia, I wouldn't go on it again.) I was on Met 500mg for less than three months before things got worse again (not that they were all that great to begin with). Why should I expect anything different from Met 1000mg? Or any other drug?
I understand that if I do have MODY (which, given my research, actually seems likely), then I'm just not on the right kind of medication. But I'll always be waiting for the day when my BG rises again, and I'll constantly be on edge because, based on how things work out for me in general, it seems like that's the only way this will end. Also, I don't like the look of the side effects of the sulfonylureas (specifically weight gain and constant hunger--I can deal with the hypos).
I know that, technically, my BG on Met isn't "that high", but I'm still at my wit's end. And, as I've said before, if it weren't for that darned c-peptide, I'd have been begging for insulin in October. I was ready to beg for insulin, actually, before I heard how high my c-peptide was.
I'm also frustrated with the fact that I don't have much control over the foods I eat and when. Today was the kind of day where I had a protein bar for lunch on the train. Sometimes I'll run in to Target for a yogurt. Sometimes it's tuna and crackers, and sometimes it's pizza. (For the record, tuna and crackers, about half the carbs of pizza, with like 10 times more protein, annoys my BG more than pizza does. That tells me that pizza is the better option?) I feel like insulin might give me a little more freedom (and maybe a little less guilt) on days where the choice is between a yogurt (and then being hungry all day) and a grilled chicken sandwich (where at least I stand a chance but will ordinarily wreak havoc on my BG).
Has anyone else felt like this, long before they maxed out the doses on all (or most) of the available options for oral meds? Is it "weird" that I feel like this?