Winterwatch
Well-Known Member
- Messages
- 50
- Type of diabetes
- Type 1
Hi @Winterwatch ,
Yep, I've been there... They assume by "the book" you are having too many hypos to acieve the A1c.. Felt like I couldn't win.
I am hypo aware, even whilst sleeping. Had no more than usual & never in my time needed intervention (even as a child.) with lows...
Hats off for your result. I've not driven mine al low as yours.. But still below the recomended "benchmark."
Hi Jaylee, thanks for the reply. Out of interest, what do you (or others if you know) tend to consider to be a hypo? I think my hospital's main concern is that I lose hypo awareness. As it is, I usually get symptoms at around 3.6, which probably coincides with that being the low alert setting on my CGM. I would normally also correct a high 3 (i.e. 3.8/3.9) as and when I see it, but wouldn't consider that to be a hypo or a negative result.
Yes, all the time, only been diagnosed for nearly three years and have been in the low 5's for the last two years. My first consultant was very judgemental and never listened. The second one is younger and is more supportive but he wants me to start having higher numbers. My DSN was horrific and so glad she has moved on. I am super sensitive to going low and high, and happier in the middle. At this stage I am not after any support, well given up wanting any, just want my results and enough test strips, (they are trying to limit them).I am wondering whether anyone else gets a hard time from their hospital for their A1c being "too low".
By way of background, my stats since diagnosis in February 2017 are:
February 2017 - 10.5%
April 2017 - 6.7%
August 2017 - 4.5%
March 2018 - 4.5%
October 2018 - 4.5%
The only result that my hospital have been happy with was April 2017 (which was elevated because it was so soon after diagnosis). For the three most recent visits, I've essentially been told to loosen my control because the numbers are too low. Given that A1c is an average, I don't know how they can make the assumption that I must be having frequent hypos - in fact, I am in range 98-99% of the time (3.6 - 6.7 mmol/mol). Not only do a get a hard time about it at the appointment, I then get a letter written about it to my GP each time.
Just one example - they say I should be between 6.5 and 8 mmols before bed. At best this seems overly cautious (especially if you know you tend to rise a bit over night). At worst, it seems irresponsible. I wonder whether this kind of advice is aimed at covering their own liability. I understand that not everyone tries (or is able) to achieve non-diabetic levels and that the standard guidelines may be appropriate in most cases. But if someone wants to do better than that, I don't see why they should not support that.
It's highly frustrating to put in so much work on a daily basis to have it disregarded. Saying that, I haven't been able to see the consultant since my diagnosis in February so perhaps he would take a different view. I am intending to take a print out of my daily stats next time to see if that alleviates their concerns.
Anyone else get this? Do you just continue to do your own thing and put up with the visits?
which probably coincides with that being the low alert setting on my CGM.
I am wondering whether anyone else gets a hard time from their hospital for their A1c being "too low".
By way of background, my stats since diagnosis in February 2017 are:
February 2017 - 10.5%
April 2017 - 6.7%
August 2017 - 4.5%
March 2018 - 4.5%
October 2018 - 4.5%
The only result that my hospital have been happy with was April 2017 (which was elevated because it was so soon after diagnosis). For the three most recent visits, I've essentially been told to loosen my control because the numbers are too low. Given that A1c is an average, I don't know how they can make the assumption that I must be having frequent hypos - in fact, I am in range 98-99% of the time (3.6 - 6.7 mmol/mol). Not only do a get a hard time about it at the appointment, I then get a letter written about it to my GP each time.
Just one example - they say I should be between 6.5 and 8 mmols before bed. At best this seems overly cautious (especially if you know you tend to rise a bit over night). At worst, it seems irresponsible. I wonder whether this kind of advice is aimed at covering their own liability. I understand that not everyone tries (or is able) to achieve non-diabetic levels and that the standard guidelines may be appropriate in most cases. But if someone wants to do better than that, I don't see why they should not support that.
It's highly frustrating to put in so much work on a daily basis to have it disregarded. Saying that, I haven't been able to see the consultant since my diagnosis in February so perhaps he would take a different view. I am intending to take a print out of my daily stats next time to see if that alleviates their concerns.
Anyone else get this? Do you just continue to do your own thing and put up with the visits?
I think this is common. I share your frustration... It's almost like they expect type 1s to have bad control.... I've often felt they suspect I'm lying when I say I don't have bad hypos.
I can't afford libre or don't think I need one for daily management but my plan is to get one twice yearly before consultant appointment just so that I can prove that I'm not having hypos.
With my driving license renewal coming up, I don't want to take any chance. It's also difficult because I get different consultant each time.
I keep non-diabetic bs eating low carb - Hba1c 5.3%
Yes, all the time, only been diagnosed for nearly three years and have been in the low 5's for the last two years. My first consultant was very judgemental and never listened. The second one is younger and is more supportive but he wants me to start having higher numbers. My DSN was horrific and so glad she has moved on. I am super sensitive to going low and high, and happier in the middle. At this stage I am not after any support, well given up wanting any, just want my results and enough test strips, (they are trying to limit them).
I have gone in with all the information to alleviate their fears and they still ask if I feel hypos. Sending you loads of support and hope they start supporting you, well done for doing so well.
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