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I quite often check Libre with finger prick. Libre measures interstitial glucose level which is not the same as blood glucose. I can usually tell when Libre is misbehaving and, therefore, I finger prick more often.
I also remember, when first diagnosed, how much better I felt after having some insulin!
I began injecting myself very early on and I was 4 weeks away from my 9th birthday when diagnosed. I refused to inject the orange thinking it would be more beneficial to inject myself!
Hello Jonathan G
I totally agree about about the orange and also agree about injecting myself
Sometimes I find it a pain to do
But then I am still alive
Like I said things have come a long way since those days
For that I am truly grateful
I personally don't think they will ever find some mircle cure either tablet or injection
To rectify this condition
It seems world wide it's growning with more people becoming diabetic one or two
And not to sound morbid I have had a good life
 
You should have test strips if needed already though, abbot are quick at sending replacements
Abbott were NOT quick at sending replacements between c. Feb '21 to c. Jul 22. Their representatives on the phone lines were clearly constrained by "the script of responses they had to follow" and 7 working days was their "norm". At least my expectations were managed, albeit not with a solution that was satisfactory for me. If there is now an improvement on their service delivery that, of course would be welcome - but wouldn't change my opinion that adult Patients and carers of minors should be allowed to hold a reserve.
and as it sounds like there are a lot of failures for this person, if theyd been reporting them all along theyd already have spare sensors.
I'm confused by your remark about this person (me [and I don't take sugar[) reporting failures all along. Who, exactly do you think I should have been reporting these failures to? In theory Abbott already knew, since their records showed I was regularly requesting replacements. Reporting anything to the NHS is not just a waste of time and energy, there is no evidence that somebody with responsibility even knows what the users have to tolerate.

Your comment about already having spare sensors is what my original response was all about and I don't see why you are challenging my remarks. Am I missing something?
If i run out of sensors due to failures and didnt have a spare, i'd just fingerprick for the 1-2 days until the replacement arrived.
Curiously, because I had a thoroughly unpleasant 1st year without CGM I did at least do my apprenticeship in managing with only fps. I wouldn't choose to go back to that world. I also very regularly tested my hypo awareness! It seems that some people now do get CGM from a very early stage after their diagnosis. That is great, in principle, but it does leave some people far from well prepared to manage only with fps. No doubt they will survive. That is sort of akin to saying you have a car but the windscreen urgently needs cleaning - but it's OK to manage for a couple of days. If a patient needs a reserve sensor then it should be prescribed and the person authorising such a prescription should search their moral compass and apply medical judgement and write the script. Regardless of whether it is only 2 days or nearer 10. Nobody should be forced to unnecessarily go hypo (or hyper) just because an HCP won't exercise the judgement implicit in the training and authority they have spent years receiving.
 
It’s April 2024 so not sure of the relevance of this?
The relevance, @Lucyr, is that you commented that Abbott were relatively speedy and that was not my experience; ever. It was part of your wider comment that we should manage without having a reserve sensor. That is not a principle that I support.

How about explaining who (and how?) I should have been reporting all these failures to? That was another remark you made which, if I'm honest about this, irritated me no end.

You are entitled to offer an opinion - but not dictate what someone else must do. I remind you of your original contribution:
You should not be asking your GP surgery to issue extra prescriptions to cover failed sensors. Your GP should only be issuing 2 sensors per month regardless of how many failures you have. Any failures or falling off early you need to report to abbot to get them to replace.
I said at that time that I thought your response was a bit too rigid. You see many things as "black and white", "right or wrong". Alas in the real world so many things are not so clearcut, no matter how one might wish they were / are. In this example GPs could and in my opinion should exercise judgement and apply some common sense. If an individual is happy to muddle through without a reserve sensor that is their prerogative. I wasn't happy to regularly be returned to that position and when having over 50% failure rate I found that downright unacceptable. I appealed to my GP and that appeal was heard and resolved. With CGM I can generally achieve 70+% TIR; without CGM I rapidly could return to the "roller coaster" of serious lows, high rebounds then lows again. An unnecessary stressful situation. Just the constant finger prick checking and monitoring is a major intrusion on my daily living and my need to do that checking was inevitably intrusive on my wife's daily living.

I would be happy to park this dialogue now and accept that we agree to disagree.
 
How about explaining who (and how?) I should have been reporting all these failures to? That was another remark you made which, if I'm honest about this, irritated me no end.
You report the failures to abbot, using the online form or by phoning them. The delivery speed in 2021 is irrelevant as abbot have vastly ramped up their processes since 2021, only ever takes me a day or two now from filling in the online form to receiving the sensor.
 
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