- Messages
- 9,267
- Location
- Worcestershire
- Type of diabetes
- Type 1
- Treatment type
- Pump
- Dislikes
- Hypos, rude people, ignorance and grey days.
I'm impressed by your defence of a "too low" HbA1c, though I'm not sure what an HCP can do to stop you having a lower HbA1c than they want, confiscate, or ration, your insulin? send someone round to force you to eat carbs? make big pizzas and pies compulsory?
Maybe this is the reasons CCGs are having so much trouble agreeing to fund Libre, it's a massive shift of control, away from the HCP to the patient, perhaps they just can't handle it.
When we had our "inducation" for libre I remember the doctor it jokingly saying you won't need us any more soon, as technology allows you to monitor your own health more and more, but maybe this is the root of the problem.
Thanks Alison - i'd actually enjoy being told to eat pizza and pies if given the chance tooAlthough the reality would mean i'd probably end up high as a kite for 2-3 days afterwards !! (favourite saying is I need drugs to stop me getting high..)
I am not so sure that CCG's are so concerned about control and who becomes responsible as it is very much down to the individual, it is mostly a cost issue having discussed this with a few nurses at my last pump meeting, also with my particular CCG it is also the variation on readings on the libre and the time lag. Every time I see/speak to my DSN I always give her a run down on how my management has changed/improved on the basis of using the system and she can see how important it is in my control, if she could access it for me she would but in my CCG there is unlikely to be any funding available for the next 2 years.
My case as it stands now is presenting a very credible picture for what CGM's can do to improve many aspects of diabetes control, whenever I speak to a GP/nurse/consultant, to help promote this for the wider insulin dependent audience. I wasn't in full launch mode today as my brain was signalling in the background telling me to ease off the glucose gas, but it was great to hear a GP say this and without hesitation to discuss the benefits of why my 42 doesn't impact on my hypo awareness due to the fact that I have less of them and they are less severe than when I was trying to fumble around in the dark ricocheting with levels of 2.2 to 18 (that's my control at it's worst when trying to live normally with injections and a meter and a moderate to high carb diet). Yes there's a combination of factors involved in control but being able to see a moving picture of your control is very empowering if used in the right way.
morning all, 9.9 last night, 8.8 this morning, guess I'm aiming for 7.7 at lunch!
Fail!
also with my particular CCG it is also the variation on readings on the libre and the time lag.
Right this diabetic lark is getting on my nerves now. I have an appointment with hospital a week on Tuesday at the pump clinic with a view to being put on a pump. This is mainly due to unpredictable dawn phenomenon; I can go to bed with a 5.5 and wake up with a 13!!!!. It does happen intermittently however, but on a fairly regular basis.
Now for the past 10 days or so after speaking with DSN, she told me to start injecting my evening Levemir in my bum and area i had not used a great deal before. Ever since then my control has become really good. Bedtime 5.5, early hours maybe 6.5 then dropping back to 5.5 when i get up. Even my daytime BG have been fairly good, within 4--7 most of time except for small spike straight after eating before falling back. This is despite taking around 15% less Levemir.
Now if i go to pump clinic at end of month and if i keep up these decent BG are they going to turn round and say, your control is good why should we give you a pump.
Like Helensaramy has experienced, is better having poor control and getting all of the tech to help you
Not content with the tinkering I've done in xDrip so far, I've spent some of this morning setting up a Nightscout site to upload the data too. I intend to use this to gain reporting functionality which xDrip doesn't really show much of.
They look much more comprehensive than what you get in xDrip+ and I've been able to backfill data from the day my current sensor started. Can share more details in a PM if you like?Be interested to know what you find out or what the reports do show.
Yes yes on my list of "things to do" but at the moment I'm distracted by pork pie.
They look much more comprehensive than what you get in xDrip+ and I've been able to backfill data from the day my current sensor started. Can share more details in a PM if you like?
Yep, I am interestedThey look much more comprehensive than what you get in xDrip+ and I've been able to backfill data from the day my current sensor started. Can share more details in a PM if you like?
Right this diabetic lark is getting on my nerves now. I have an appointment with hospital a week on Tuesday at the pump clinic with a view to being put on a pump. This is mainly due to unpredictable dawn phenomenon; I can go to bed with a 5.5 and wake up with a 13!!!!. It does happen intermittently however, but on a fairly regular basis.
Now for the past 10 days or so after speaking with DSN, she told me to start injecting my evening Levemir in my bum and area i had not used a great deal before. Ever since then my control has become really good. Bedtime 5.5, early hours maybe 6.5 then dropping back to 5.5 when i get up. Even my daytime BG have been fairly good, within 4--7 most of time except for small spike straight after eating before falling back. This is despite taking around 15% less Levemir.
Now if i go to pump clinic at end of month and if i keep up these decent BG are they going to turn round and say, your control is good why should we give you a pump.
Like Helensaramy has experienced, is better having poor control and getting all of the tech to help you
Actually the only reason I used "carp" was because I couldn't remember all those names we made up for various swear words
We never fail bro.Fail!
You can't use your bum forever, so there is still an issue with other injection sites. This does show that injection sites are an issue for you, and if I recall that was what the doctor said when he recommended you for a pump.
I think this is a really difficult one. If I remember correctly, @smc4761 has had diabetes for over 30 years, same as me. When I asked the nurse consultant how long it'd take for my lipohypertrophy to disperse, shel ooked at me and said, 'how long did it take to develop'? as in, it's not likely to disappear in my lifetime. So I've scrabbled around for new sites and at the moment I'm managing. Injecting in some places, like my bum, is an option but it has problems for me: seeing what I'm doing in certain areas, and managing to keep track of where I've injected so I don't end up injecting repeatedly in the same place. I find that so much easier in my abdomen and to some extent my arms. Thighs are out as for some reason absorption seems quite erratic there. So even if it's working now for @smc4761 , if it was me I'd be wondering how long that would last. And I'm not sure how you measure who really needs a pump...@smc4761 if your control stays good do you really need a pump? - when someone else who might really need it doesn't get one.
I know we would all like to have the latest and greatest tech
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