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Access to test strips - can you logically answer 'no' to these questions?

Alternatively @Brunneria there's always the gentle reminder that 80% of obese people are not diabetics so therefore using that rationale, there's a lot more to the whole situation than someone simply eating themselves into this condition!

Good point. But how many of that 80% have comprehensive glucose tolerance tests?

Bloodsugar101 describes a number of different ways that impaired glucose tolerance starts to show itself - and a raised fasting BG is often not a symptom until quite late in the process - with full blown type 2 usually coming very late, after years of identifiable evidence (but not nec years of raised fasting BG).

But it is unrealistic to expect a pressurised NHS to give people those tests - heck, most identified pre-diabetics are lucky to get a test annually (my doctor seemed surprised when I reminded him that I hadn't had one in 3 years, and my father was told he was 'normal' with a fasting BG of 6.7, no need for follow up).

A comprehensive set of tests would include an extended oral glucose tolerance test, over 4+ hours. And several fasting tests, over different days and different times.

It just isn't going to happen.
 
Hello to everyone, I have only just found this series of posts on T2, should/should'nt test. When I was first diagnosed I was given a meter and strips straight away, and that has has continued, it has always been my absolute belief that all diabetis should have testing meters and strips.
Infomation is the basic need to keep this under control, in all aspects of life.
Diabetes is a very bad condition and by not monitoring it, can give a false feeling of it's ok to just put the blinkers on and ignore what is going on within your body.
The NHS is founded by central govenerment, who as we all know is tightening the belt si much that very soon it won't work at all. The tories are notorious for wanting to sit on their piles, which is the only way they feel comfortable, the bottom line has lots of money in it.
The condition is not monitored and kept under control, could well result in blindness, (RNIB needs more guide dogs) amputations, (more false legs, joints etc). So we the sufferers of this condition must make the doctors and nhs start to support us, in a proper manner, we want to test and keep our eye on our bs results and keep records of what happens like being 7.1 then starting to shake, sweat, tremble and know that a hypo is getting going big style, then testing expecting to find bs in boots, but it's only 5,?, what a surprise, with out my meter I would have been panicking. or maybe even using a hypo kit to bring the bs levels back up, when it was not needed, maybe just the effects of the heat and going a lot on a very hot day, good data = right responses to the situation and no panic stations.


So I agree with all that has gone before this post, information is vital to such a body ruining condition, and testing is vital to the picture, some gp's dont want to spend money onwhat they see as a waste of resources, they are not the ones with the condition. Not all t2's could afford to pay for their own testing strips, as their financial situationis on the tightside of things. I have been very fortunate to have replied for a testing meter on 2 occasions and been sent both from different companies, and these are clever types that can down load the data direct to your computer records.
One seems like a general type, and the other is the cartridge type for t1 insulin dependant people, maybe I could give these away to somebody who needs them.


All diabetics stand up and demand equal treatment and equal support equipment, it is vital to our health and wellbeing.
2015 get the tories out and maybe labour will be able to reverse the damage that has been done, just like tony b did in 1997, after the damage by the previous tory govenment damage, ttfn
 
I was on test strip via prescription and i got a letter saying from the docs saying that it was not necessary and they would give me one a week instead of unlimited.
By then i knew how to control my diabetes and what spiked me and what did not and what to eat when.
So i shot them a letter complaining that they were treating me as a number and not an individual. It made no difference but let me vent my feelings.
I travel abroad constantly and find the need to test more than once a week so i get more if i need them but it takes some persuading but i don't give up.
But i have to say now i understand my body and food i can get away with once a week testing. I have it under control as my figures show.
We are all different that is my story it may be different for you.
 
 

My dad is a type 2 diabetic and he hasn't been given a meter, test strips or any medication. He eats very healthily and is always on the move and the result is that his blood sugar is always in range. Given this, perhaps some DN experience a dilemma as to whether the above gadgets are needed for type 2's as some are in remission and some people are struggling?
 

Those struggling need meters to help them get on track. Those "in remission" need them to help them stay there. There are very few "in remission". In any event, they should be given out at the time of diagnosis, when they are most needed.
 
Those struggling need meters to help them get on track. Those "in remission" need them to help them stay there. There are very few "in remission". In any event, they should be given out at the time of diagnosis, when they are most needed.

I can agree with that, but in my Dad's case, it seems like he's the exception to the rule. As a type 1, I've offered to let him use my blood glucose meter and he always refuses as his blood sugar is within range when he has his diabetic review. I've even asked him if he misheard the Dr. when HE says he was diagnosed with type 2!
 

Good luck to your dad, I hope he manages to stay that way. You can take a horse to water, but you can't make him drink ......
 

Can I ask what his numbers are?

Only 'being 'in range' sounds fantastic, but it rather depends what that range is.

I aim for lower than the NHS guidelines (with varying effect) because the reading I have done suggests that NHS guidelines are not low enough to prevent the onset of complications, in the long run.
 
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I was diagnosed with type 2, 16 months ago , after being rushed into hospital after having 2 heart attacks at home ,the hospital gave me a tester and strips b4 I came home and was showed how to use it ,my doctor always gives me strips and tester on script when I ask ,although he and my diabetic nurse do say I do not need to to it everyday or every week ,, although when I had a few hypos he did ask me to check everyday for 2 weeks as he had changed my medication so he could see how I was doing on the new meds still confused with my new way of life at moment ,and new to this site ,hoping to pick up some useful information to help me through this ,confused.com
 
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