I didn't have diabetes initially (I couldn't have been accepted into the military if I had). I started on pills as type 2. But the pill started failing me after only about one year. Now insulin is the only thing keeping me going. It probably makes me a type 1, don't you think.No idea what type you are hun, but as you know were all different when it comes to how insulin works or doesn't work for us.
I didn't have diabetes initially (I couldn't have been accepted into the military if I had). I started on pills as type 2. But the pill started failing me after only about one year. Now insulin is the only thing keeping me going. It probably makes me a type 1, don't you think.
I find something interesting in the details about you that were included in your post. You show a single Lantus dose of 100. For years I've been taking one night dose of 20 units. Long in the past, I tried upping it a little at a time and stopped at 30, but seeing apparently no difference, I went back to the 20 I was advised to use. How did you work up to 100?
http://www.diabetes.co.uk/difference-between-type1-and-type2-diabetes.html
was told positive for Celiac cut the gluten and my numbers went into normal range but now its finding a lower dosage that still is effective, but so far it seems that the 100 units though at times to much and causing me to hit in the 30s (spent a week when ill unable to get above 80 - was between 32 and 50 for the week - long enough that we cut my lantus dosage from 100 to 50units with humalog as needed after getting better again of course my body no longer liked the 50 units and my numbers started to rise again each morning so back to 100 units. We're right now working to find the right amount that will keep me during the day - which might mean a split dosage eventually but he doesn't won't to do that as yet. He wont's a full year of being Gluten Free to have my body settle in with whats happening (cause it can take that long for gluten to get out of the system fully.
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I'm not expert but my mom is a T2 (80s years old and 100% diet controlled and always has been she's never been on insulin or medication for it, just watching what she ate) and when she was first told she wasn't even over weight (she was at normal weight for her height. A friend of ours thinks that her's was caused my stress since no one in her family on either side was diabetic (cancer in the family yes, but no diabetes) so when she got told she was diabetic it thought her for a loop to say the least (out of left field the diagnoses came), So when I gold told D as well I assume T2 not T1 since no history on either side of my family lines other then my mom being T2.
Personally I think there might well be triggers for T2 just like there might be for T1 that makes it appear out of apparent no where. Wether it be a gene that gets turned on or off or something that is already inside us that just needs that trigger point to be activated (i think this because of how many native people I know who have D, yet it was virtually unheard of before settlers came over - so makes me think environmental as well as something in the food that's eaten are triggers, and the more diverse the population gets the more possible triggers one is exposed to in their life that could trigger it or other medical conditions).
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