debs248
Well-Known Member
- Messages
- 486
- Location
- Southampton
- Type of diabetes
- Other
- Treatment type
- Non-insulin injectable medication (incretin mimetics)
- Dislikes
- Hypocrisy, mornings
I post here because my family don't want to listen, but there are things I want to get off my chest. That seems to me to fit the ethos of a soapbox.
They're under stress themselves and just don't have or aren't prepared to make enough time for me to have a moan.Has your family indicated why they don’t want to listen?
Yay for small wins. I try to spot positives but I can't see any caused by removing testing supplies from my repeat prescription list. Except that it led me to discover a "request prescription" option on the surgery's econsult system. But I'd still rather not to have had to iyswim.As a T1 I’ve been suggesting for a few years (with my “receipts.”) I need a pump as I actually need fractional insulin doses instead of adjustments in whole units? (At certain times of the day.)
I’ve just recently been prescribed half unit pens for basal & bolus..
lol, probably a step forward to that mirage of a pump, I suppose..
OK. My wife is a “swan.” Great woman. Paddles to keep afloat.. Neither I or my wife are getting any younger.. lovely woman. I do what I can to let her follow the river..They're under stress themselves and just don't have or aren't prepared to make enough time for me to have a moan.
Sorry you are going through this, but I had to laugh at the "novel cowritten by Orwell, Heller and Monty Python" as my surgery is unfortunately the same! Had to fight to get my Triglycerides result. Onwards and upwards xxxOh and apparently I can no longer use the home phlebotomy service because I left the house when the surgery *insisted* I come in immediately, back at diagnosis. It's like living in a novel cowritten by Orwell, Heller and Monty Python.
I was correct nobody phoned, but at least I can see my blood results in the NHS app. My HbA1C is down on last year so that's good.Totally agree. I had my assessments last week and was told the diabetes nurse would call me when they get the results, I'm not holding my breath.
Does your surgery have an active Patient Participation Group? All surgeries should have one but some are more active than others. The system at your surgery does sound inefficient. Do look into the PPG and tell them what you’ve just said here. It’s the sort of situation that the PPG should take up with the surgery.Not had a rant here for a while about my "special" GP surgery but hubby is sick of me complaining so I'll post here.
My first diabetic review since diagnosis in late April is apparently due on 17th July. Not sure how they figure that out as I still haven't had an initial assessment.
Anyway, having read up for myself about diabetes, here and elsewhere on the Internet, about what they should have provided/ told me, I asked if I needed to arrange blood tests beforehand or take a urine sample with me.
Yes, they want the urine sample, but they will draw blood *at the review* for testing. Unless they've got one of those fancy fridge-sized instant HbA1c testing machines in every surgery, what's the @#*&% point of doing it then?
My FBG is almost always in double digits and i'm on the maximum dosage of Metformin, so I'm pretty sure another medication is needed, but it'll be pure guesswork on everybody's part.
I'm not asking for special treatment or even anything particularly difficult, but really, is it too much to ask for basic common sense?
The system at your surgery does sound inefficient. Do check your see if they have an active Patient Participation Group. All surgeries are obliged to have one but some are more active than others. It’s amazing how few patients know about these Groups. Do tell them what you have said here and they should then take it up with the surgery. My PPG, of which I am Secretary, meets bi-monthly with a GP, Practice Manager and other surgery admin staff present so we are able to discuss any issues raised.Not had a rant here for a while about my "special" GP surgery but hubby is sick of me complaining so I'll post here.
My first diabetic review since diagnosis in late April is apparently due on 17th July. Not sure how they figure that out as I still haven't had an initial assessment.
Anyway, having read up for myself about diabetes, here and elsewhere on the Internet, about what they should have provided/ told me, I asked if I needed to arrange blood tests beforehand or take a urine sample with me.
Yes, they want the urine sample, but they will draw blood *at the review* for testing. Unless they've got one of those fancy fridge-sized instant HbA1c testing machines in every surgery, what's the @#*&% point of doing it then?
My FBG is almost always in double digits and i'm on the maximum dosage of Metformin, so I'm pretty sure another medication is needed, but it'll be pure guesswork on everybody's part.
I'm not asking for special treatment or even anything particularly difficult, but really, is it too much to ask for basic common sense?
You’re lucky you get all this. I haven’t had a foot check for over 5 years! Likewise HBA1c is either done or not, they are incredibly lackadaisical, and that is the hospital diabetes consultant’s clinic! Before Covid, we got all the checks recommended, these have slowly dwindled over the years.My diabetes reviews are done in two parts. Part one, urine test, blood pressure, foot checks, weight and blood taking with a health care assistant. I then attend a week or so later for part two with GP, nurse or pharmacist to discuss the results of the tests taken and any need to alter medication. I wonder if your surgery works that way too and you’ll have to book the second appt once you’ve had the first appt.
Having said all that it is remiss that you’re only being seen for your first ever appt two months after diagnosis.
Edit for typo
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