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Do daily BG readings actually matter that much?

If you buy the sd Codefree strips direct from the supplier they are even cheaper than eBay or amazon. I'm not at home but I think the site is www.homehealth-uk.com. There's a promo code on the lid of the box and if you type that in on the order the strips are nearer £5 for 50.


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It's home health on ebay where I get the strips! At least I know for next time as I've thrown the box away! Many thanks :)
 
Although I am a newbie I have found no evidence so far that suggests there is a way to reverse this condition - otherwise surely everyone would be doing it? Hopefully such a breakthrough will be made one day.

I'd love to be off the meds but my GP thinks I need them so because of that I am in the health care system, but my original point of this thread asked whether that means I need to be personally adding to that system by testing, or simply rely on the advice of my GP every 6 months or so.

A more lively debate than I imagined, but overall the strongest opinion is to voluntarily test to enable me to work out what I should or should not eat which seems sensible and educational in these early months of my new ailment. I think its time to sort out a meter! Thanks all.

Great decision Phil. You will have a learning curve as you take readings, but if you keep asking questions there are loads of people on here who can help you understand what's going on.

:)
 
Although I am a newbie I have found no evidence so far that suggests there is a way to reverse this condition - otherwise surely everyone would be doing it? Hopefully such a breakthrough will be made one day.

I'd love to be off the meds but my GP thinks I need them so because of that I am in the health care system, but my original point of this thread asked whether that means I need to be personally adding to that system by testing, or simply rely on the advice of my GP every 6 months or so.

A more lively debate than I imagined, but overall the strongest opinion is to voluntarily test to enable me to work out what I should or should not eat which seems sensible and educational in these early months of my new ailment. I think its time to sort out a meter! Thanks all.

The good thing is that if you don't find testing regularly useful, you can stop at any time. And you'll only be out of pocket by a few quid.

Priceless.
 
I'm not too sure if I should have started a new thread as I'm a newbie who is still coming to terms with T2. I'm really not sure what my symptoms are, I feel fine except for urinating more and being a bit solid in the others. I'm undecided about testing but wondering if I should start just to find out what is going on. Had my chat with Diet Nurse today and she suggested waiting for my second HbA1c and see where I was going with diet control. She said my increased urinating was my body trying to get rid of my sugars.... so something is not so good.... although I do like cooking I do seem to eat the same things week after week... just not so much as I used to.
 
I don't have the wide experience of some on this forum, having only been diagnosed since March. My doctor and DN said that I didn't need to test, although I test once a week and have done so since the start of April. I looked at testing first thing, but decided that the 2 hrs after a meal would be a good guide. At the start I was also just adjusting my diet and have now gone fully onto the LCHF diet for the last month or so.

My readings started out at over 9 (2 hrs after a meal) and have gradually decreased as I have adapted my diet until last week when it was 5.2.

I Know that I have lost about 7ibs in weight since diagnosis and have been taking more exercise, walking in the main for about miles every other day as a brisk pace and being more active in the garden and even going up and down stairs quickly a few times a day. Not a huge change, but one that seems to be working on a graduated basis.

Some of the problems with LCHF is that I'm allergic to most nuts. I was previously fanatical about eating low fat stuff as I had previously had high cholestral, which I got under control by changing my diet to low fat. Now, I'm back eating full fat cheese, eggs etc. As I'm a veggie I always check the ingredients of what food I buy, now I also check things like carb and glucose and sugars well. Some manufacturers are quite clever at putting those items on labeling in the smallest of type, which I have difficulty in reading due to poor vision. (Not diabetes related -just very short sighted). I have adjusted the types of fruit that I eat, getting rid of the high sugar types and substituting those low in sugar - it seems to work, although I miss eating grapes, which I love, but I know, won't love me.

When first diagnosed I got very worried about the consequences of diabetes, but having calmed down and taken the measure of what I can and can't do, have struck a balance that seems to be working,. I'm on the metaformin 500g 3 times a day, but would like to reduce it if possible, but will have to wait for the next 3 month checkup, which I believe will be due towards the end of June.

I have had a couple of blips, where I have felt really unwell, but I could actually put my finger on what had caused it. Once, I had gone out for a meal and had eaten potato based foods which seemed to really affect me very quickly. Lesson learned and now a strict No, No. Than a couple of weeks ago I got a really bad cold (which is still hanging around) which seemed to cause BS to fluctuate for some reason - I presume that the battle going on in the body against the germs had something to do with that. But drinking a lot and resisting the urge to take cold or flu remedies was I believe the right one. I'm on enough meds as it is.

I can't claim to be in control, but I am serious about working sensibly both with the doctor and DN, but also with some of the wisdom available here. The other day I was in a Chemists shop and he was busy selling a BT Machine to a customer and giving her all sorts of advice about how to use it (she was apparently newly diagnosed) and insisted that she tested first thing in the morning? This seems to me from what I have read elsewhere on these forums to be a bad idea as first thing the BS is automatically raised as the body adjusts to rising and getting ready for a day of activity? I mentioned that I tested weekly and the chemist asked why (he was suggesting she tested daily - perhaps thinking of the profits when she came back for more lances and test strips). I queried that saying that my GP has said that testing was unnecessary at as T2, but he had no objection to my doing so if it gave me peace of mind. The DN agreed with that.

In the end, it's getting to know how diabetes is affecting you day to day, what food or drinks might be the trigger for raised BS and substituting others more appropriate. Becoming more active and exercising or doing practical things like gardening, etc. I now walk to the shops and carry stuff home rather than jumping in the car. Small things, combined with sensible measures seem to suit me, but might not suit or be possible for others.
 
I'm not too sure if I should have started a new thread as I'm a newbie who is still coming to terms with T2. I'm really not sure what my symptoms are, I feel fine except for urinating more and being a bit solid in the others. I'm undecided about testing but wondering if I should start just to find out what is going on. Had my chat with Diet Nurse today and she suggested waiting for my second HbA1c and see where I was going with diet control. She said my increased urinating was my body trying to get rid of my sugars.... so something is not so good.... although I do like cooking I do seem to eat the same things week after week... just not so much as I used to.

Hi,

Welcome! This forum is a fantastic source of knowledge and experience. I've learned so much!

Something I only learned recently (from a couple of people on this forum) is that the extra widdling happens when your blood glucose rises above about 10.5. Apparently that is when the kidneys start dumping sugar into the urine. Useful to know, eh?

So even without a meter you can roughly gauge that your BG is above or below that figure.

Mind you, while getting your glucose down to below 10 is a good goal, it is just a stepping stone to good control...

Have a look at some of the foodie threads. Lots of inspiration there :)
 
I don't have the wide experience of some on this forum, having only been diagnosed since March. My doctor and DN said that I didn't need to test, although I test once a week and have done so since the start of April. I looked at testing first thing, but decided that the 2 hrs after a meal would be a good guide. At the start I was also just adjusting my diet and have now gone fully onto the LCHF diet for the last month or so.

My readings started out at over 9 (2 hrs after a meal) and have gradually decreased as I have adapted my diet until last week when it was 5.2.

I Know that I have lost about 7ibs in weight since diagnosis and have been taking more exercise, walking in the main for about miles every other day as a brisk pace and being more active in the garden and even going up and down stairs quickly a few times a day. Not a huge change, but one that seems to be working on a graduated basis.

Some of the problems with LCHF is that I'm allergic to most nuts. I was previously fanatical about eating low fat stuff as I had previously had high cholestral, which I got under control by changing my diet to low fat. Now, I'm back eating full fat cheese, eggs etc. As I'm a veggie I always check the ingredients of what food I buy, now I also check things like carb and glucose and sugars well. Some manufacturers are quite clever at putting those items on labeling in the smallest of type, which I have difficulty in reading due to poor vision. (Not diabetes related -just very short sighted). I have adjusted the types of fruit that I eat, getting rid of the high sugar types and substituting those low in sugar - it seems to work, although I miss eating grapes, which I love, but I know, won't love me.

When first diagnosed I got very worried about the consequences of diabetes, but having calmed down and taken the measure of what I can and can't do, have struck a balance that seems to be working,. I'm on the metaformin 500g 3 times a day, but would like to reduce it if possible, but will have to wait for the next 3 month checkup, which I believe will be due towards the end of June.

I have had a couple of blips, where I have felt really unwell, but I could actually put my finger on what had caused it. Once, I had gone out for a meal and had eaten potato based foods which seemed to really affect me very quickly. Lesson learned and now a strict No, No. Than a couple of weeks ago I got a really bad cold (which is still hanging around) which seemed to cause BS to fluctuate for some reason - I presume that the battle going on in the body against the germs had something to do with that. But drinking a lot and resisting the urge to take cold or flu remedies was I believe the right one. I'm on enough meds as it is.

I can't claim to be in control, but I am serious about working sensibly both with the doctor and DN, but also with some of the wisdom available here. The other day I was in a Chemists shop and he was busy selling a BT Machine to a customer and giving her all sorts of advice about how to use it (she was apparently newly diagnosed) and insisted that she tested first thing in the morning? This seems to me from what I have read elsewhere on these forums to be a bad idea as first thing the BS is automatically raised as the body adjusts to rising and getting ready for a day of activity? I mentioned that I tested weekly and the chemist asked why (he was suggesting she tested daily - perhaps thinking of the profits when she came back for more lances and test strips). I queried that saying that my GP has said that testing was unnecessary at as T2, but he had no objection to my doing so if it gave me peace of mind. The DN agreed with that.

In the end, it's getting to know how diabetes is affecting you day to day, what food or drinks might be the trigger for raised BS and substituting others more appropriate. Becoming more active and exercising or doing practical things like gardening, etc. I now walk to the shops and carry stuff home rather than jumping in the car. Small things, combined with sensible measures seem to suit me, but might not suit or be possible for others.
Welcome to you too!

It looks like you are off to a really good start, and you have an understanding medical team. That is priceless.
 
Although I am a newbie I have found no evidence so far that suggests there is a way to reverse this condition - otherwise surely everyone would be doing it? Hopefully such a breakthrough will be made one day.

I'd love to be off the meds but my GP thinks I need them so because of that I am in the health care system, but my original point of this thread asked whether that means I need to be personally adding to that system by testing, or simply rely on the advice of my GP every 6 months or so.

A more lively debate than I imagined, but overall the strongest opinion is to voluntarily test to enable me to work out what I should or should not eat which seems sensible and educational in these early months of my new ailment. I think its time to sort out a meter! Thanks all.

You won't regret getting the metre.

Sent from the Diabetes Forum App
 
I don't have the wide experience of some on this forum, having only been diagnosed since March. My doctor and DN said that I didn't need to test, although I test once a week and have done so since the start of April. I looked at testing first thing, but decided that the 2 hrs after a meal would be a good guide. At the start I was also just adjusting my diet and have now gone fully onto the LCHF diet for the last month or so.

My readings started out at over 9 (2 hrs after a meal) and have gradually decreased as I have adapted my diet until last week when it was 5.2.

I Know that I have lost about 7ibs in weight since diagnosis and have been taking more exercise, walking in the main for about miles every other day as a brisk pace and being more active in the garden and even going up and down stairs quickly a few times a day. Not a huge change, but one that seems to be working on a graduated basis.

Some of the problems with LCHF is that I'm allergic to most nuts. I was previously fanatical about eating low fat stuff as I had previously had high cholestral, which I got under control by changing my diet to low fat. Now, I'm back eating full fat cheese, eggs etc. As I'm a veggie I always check the ingredients of what food I buy, now I also check things like carb and glucose and sugars well. Some manufacturers are quite clever at putting those items on labeling in the smallest of type, which I have difficulty in reading due to poor vision. (Not diabetes related -just very short sighted). I have adjusted the types of fruit that I eat, getting rid of the high sugar types and substituting those low in sugar - it seems to work, although I miss eating grapes, which I love, but I know, won't love me.

When first diagnosed I got very worried about the consequences of diabetes, but having calmed down and taken the measure of what I can and can't do, have struck a balance that seems to be working,. I'm on the metaformin 500g 3 times a day, but would like to reduce it if possible, but will have to wait for the next 3 month checkup, which I believe will be due towards the end of June.

I have had a couple of blips, where I have felt really unwell, but I could actually put my finger on what had caused it. Once, I had gone out for a meal and had eaten potato based foods which seemed to really affect me very quickly. Lesson learned and now a strict No, No. Than a couple of weeks ago I got a really bad cold (which is still hanging around) which seemed to cause BS to fluctuate for some reason - I presume that the battle going on in the body against the germs had something to do with that. But drinking a lot and resisting the urge to take cold or flu remedies was I believe the right one. I'm on enough meds as it is.

I can't claim to be in control, but I am serious about working sensibly both with the doctor and DN, but also with some of the wisdom available here. The other day I was in a Chemists shop and he was busy selling a BT Machine to a customer and giving her all sorts of advice about how to use it (she was apparently newly diagnosed) and insisted that she tested first thing in the morning? This seems to me from what I have read elsewhere on these forums to be a bad idea as first thing the BS is automatically raised as the body adjusts to rising and getting ready for a day of activity? I mentioned that I tested weekly and the chemist asked why (he was suggesting she tested daily - perhaps thinking of the profits when she came back for more lances and test strips). I queried that saying that my GP has said that testing was unnecessary at as T2, but he had no objection to my doing so if it gave me peace of mind. The DN agreed with that.

In the end, it's getting to know how diabetes is affecting you day to day, what food or drinks might be the trigger for raised BS and substituting others more appropriate. Becoming more active and exercising or doing practical things like gardening, etc. I now walk to the shops and carry stuff home rather than jumping in the car. Small things, combined with sensible measures seem to suit me, but might not suit or be possible for others.
I would test a bit more if I were you at the moment. My doc says the important one is fasting bloods ie before food or drink. Testing will help you fine tune what you eat. Your bs goes up with illness usually:( mine goes haywire! If you're eating LCHF and you feel funny - test. Because I lost weight and halved bs, I hypod because I didn't need the 3 met a day I was on. Doc reduced it down to one. Hope this helps!
 
If you buy the sd Codefree strips direct from the supplier they are even cheaper than eBay or amazon. I'm not at home but I think the site is www.homehealth-uk.com. There's a promo code on the lid of the box and if you type that in on the order the strips are nearer £5 for 50.


Sent from the Diabetes Forum App

Thank you for that link, Peacetrain:).
 
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