trophywench
Well-Known Member
- Relationship to Diabetes
- Type 1
That's hillarious!
No it absolutely ain't. This was in December 2022 - and it's HORRIFYING.
That's hillarious!
I already moved from another local GP to this one as they seemed so much better. I now just do my own research.I probably would find a new GP.
Yes completely normal, many T2s that test self fund the strips.As a Type 1 I'm amazed at the GP's response. Is this normal? How can T2's manage their diabetes without knowing how different foods affect them?
It’s really not. I’ve been told the line about “don’t test as you’ll need your fingers to read braille” by a doctor before tooThat's hillarious!
Shocking! "Don't test, we'll take care of everything" and then they don't. This forum is pure gold.It’s really not. I’ve been told the line about “don’t test as you’ll need your fingers to read braille” by a doctor before too
I don't understand this when people on insulin are told to test.It’s really not. I’ve been told the line about “don’t test as you’ll need your fingers to read braille” by a doctor before too
On diagnosis in 2000ish, but not yet on insulin, I was given a meter, standard practice then for all, and told to use only outside 3 fingers on each hand, because you will need your index fingers and thumbs if (when possibly implied) you go blind.I don't understand this when people on insulin are told to test.
Is that because we are less likely to need to read braille?
Yet another example how education about the kit helps then, but first they need to be educated themselves how to use bgm for testing foods rather than solely for insulin dosages and hypo avoidance.Another aspect of this common attitude about T2s not needing to self test may be that surgeries fear that self-testers will take up surgery time asking if it is significant that their readings have been 5.6 for weeks but have now risen to 5.8.
Hi docb,If you go back to the NICE guidelines on treatment of T2 you will find that there is no real guidance on the subject of monitoring.
Probably just assume you’ll have to struggle to read braille because of all the testingI don't understand this when people on insulin are told to test.
Is that because we are less likely to need to read braille?
Being a GP is a job. And some really aren't that good at their job. The real world.Hello everyone, I haven't posted here for a few years but I think this forum is the best place to ask my question.
My partner was diagnosed T2 six months ago and at the beginning I gave him my spare blood testing kit to keep an eye on his BG levels. I expected his GP to prescribe a test kit but he didn't.
The strips are now finished so he asked his GP for a prescription. His GP refused telling him he doesn't need to check his BG! He will have his bloods checked every 3 months and that's enough. He doesn't need to stress over his BG levels.
As a Type 1 I'm amazed at the GP's response. Is this normal? How can T2's manage their diabetes without knowing how different foods affect them?
Maybe there is a change of policy for T2's but I thought you got one box of test strips per month?
Hi docb,
The question for me is, does self testing t2's provide information that could be used to improve control? If so, then on health grounds, surely the NICE advice should be clear, that testing should be made available.
My brother, T2, was distinctly advised to use the sides of fingers and avoid fingertips BECAUSE we all need the sensitivity of our fingertipsfor everyday sensitivity and dexterity.Being a GP is a job. And some really aren't that good at their job. The real world.
And a productive discussion relies on others taking on-board what you have to say. Not throwing any stones.My brother, T2, was distinctly advised to use the sides of fingers and avoid fingertips BECAUSE we all need the sensitivity of our fingertipsfor everyday sensitivity and dexterity.
If HCPs have somehow lost sight of that fairly obvious rationale, this is a huge shame - and something of a disgrace if true. But at the very least we can quietly explain and educate those who might have been misled.
Hi,It depends.
I was diagnosed with a hba1c of 83, bought a meter, did a few tests, and then didn't do any for three months.
I just changed 'lifestyle' and lost weight.
Next hba1c was 36.
Just before the blood test I used a trial Libre and the first reading I saw in the 5s.
After a week I knew things had come under control.
Maybe I was just lucky in that the weight loss/diet change got levels back down.
I certainly had no idea what was going on for 3 months.
The lack of being able to act freely began long before covid hit.Hi,
Of course, if someone chooses not to test, be that by circumstances or just not wanting to test that is their right. The question seems to be about blanket GP decisions not to allow type 2's to self test, regardless of circumstances. If testing can help in their control, then nothing wrong with clear guidance being given (NICE) making self testing available to those that wish to test?
There again, just becasue the NICE guidance is unclear, a GP in practice can "practice" what they see fit based on their experience and good judgement. Although we seem to have moved away from those medicallly trained, being able to freely act on their own good judgement and instead blindly following official guidelines, following covid.
Hi,
Of course, if someone chooses not to test, be that by circumstances or just not wanting to test that is their right. The question seems to be about blanket GP decisions not to allow type 2's to self test, regardless of circumstances. If testing can help in their control, then nothing wrong with clear guidance being given (NICE) making self testing available to those that wish to test?
There again, just becasue the NICE guidance is unclear, a GP in practice can "practice" what they see fit based on their experience and good judgement. Although we seem to have moved away from those medicallly trained, being able to freely act on their own good judgement and instead blindly following official guidelines, following covid.
Wow! there's another question for another discussion. If those diagnosed are not even told about testing, then they can't even make an informed decision to test or not. Got to say, i'm very suprised by some of the points raised in this thread about availability and advice on testing.Testing has never been mentioned to me.