I decided to go to see the GP today, for two reasons:
1. Discuss my metformin dose in the light of my recent HbA1c result (35). Presently on 2 x 500mg.
2. To find out why I'm getting dead hands most nights.
I managed to get a 6:50 evening appointment with a doctor I'd never met. It didn't bother me because I've never met most of them, not even my own GP.
When I explained my 6 months old diabetes history, he was very impressed and asked how I had achieved it. I just said I had monitored my bg levels and lowered my carb intake. He didn't bat an eyelid and said he wanted to put me on a pedestal ha ha.
We discussed the metformin and he has agreed to lower the dose to one 500mg dose per day. He has changed the type from ordinary to modified release because he said one a day is unusual. I hope they agree with me because I've been fine on the ordinary ones.
He then went on to explain that I shouldn't see my goal as being medication free as it wasn't that important. I understood that because I have read the debates about it here but I just feel I need a further challenge. He then went on to reinforce the fact that medication will be inevitable further down the line ... Progressive ...
As far as the dead hands go, because it begins on the side of my little fingers, he's ruled out carpal tunnel. He's banged my elbows, arms etc and checked out my neck. I now have a prescription for diethylamine salicylate cream and I have to massage it into my elbows 3 times a day. It's an anti inflammatory and he said to stop taking it if I get indigestion or heartburn. If there's no improvement I may have to have conduction tests (??)
The doctor also said if my bg levels began to creep to 40 or 45, I would have to go back to 2 x 500mg. (He said he's scared the nurse will tell him off!!)
His comment about the progressive nature of D has depressed me a little. I always knew it and understood but I was trying to put it to the back of my mind. I really don't want negativity to creep in to my thoughts.
Now I'm going to walk a portion of the 42.
Sorry if I've rambled.
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What has knocked you peacetrain? Your doc's "progressive" comment?
I conclude that many of our health car professionals have extremely low aspirations for we T2s. I can't comment for T1s as I haven't any personal experience. My take is that they routinely see a significant proportion of individuals who follow their advice, and can't achieve the sort of control many of us have achieved. And that'll be those who actually do something. I can't recall the stats, but I believe a significant proportion of T2s make no lifestyle changes when diagnosed. On those basis, it can be easy to see how expectations fall short of our higher than normal standards.
Of course, I may be doing our medics and fellow diabetics an extreme disservice. But, it's the only conclusion I can (un)comfortably reach.
Personally, I'll be doing all I can to control this flippin' thing. I have it on a tight leash, and I'm watching it like a hawk. I can do scary.
Chin up.
There's also the fact that the "official" advice on diet handed out to eat carbs, carbs and more carbs is almost a guarantee that the disease will continue to progress.
I'm sure these HCP's firmly believe the party line that they trot out - simply because they meet so few people like you who actually take charge and change their lifestyle.
Thanks for your support. So grateful.hi Peacetrain,
I don't post here that often, but just wanted to say how much your reaction to your doctors reinforcement of the "inevitable decline" message was just like mine. I'm sure they think they are doing their best, to avoid a crushing disappointment for those for whom it becomes true, but it was one of the most depressing things I had heard from a HCP since I was diagnosed (I heard this from our local hospital diabetic consultant at a DUK information day). I got really upset at the time, but was then more resolved than ever to try to prove them wrong!
Perhaps if enough of us manage to keep our HbA1c down, they might eventually have to change their stats.
Keep up the good work - sounds like you are doing great.
Sue
I decided to go to see the GP today, for two reasons:
1. Discuss my metformin dose in the light of my recent HbA1c result (35). Presently on 2 x 500mg.
2. To find out why I'm getting dead hands most nights.
I managed to get a 6:50 evening appointment with a doctor I'd never met. It didn't bother me because I've never met most of them, not even my own GP.
When I explained my 6 months old diabetes history, he was very impressed and asked how I had achieved it. I just said I had monitored my bg levels and lowered my carb intake. He didn't bat an eyelid and said he wanted to put me on a pedestal ha ha.
We discussed the metformin and he has agreed to lower the dose to one 500mg dose per day. He has changed the type from ordinary to modified release because he said one a day is unusual. I hope they agree with me because I've been fine on the ordinary ones.
He then went on to explain that I shouldn't see my goal as being medication free as it wasn't that important. I understood that because I have read the debates about it here but I just feel I need a further challenge. He then went on to reinforce the fact that medication will be inevitable further down the line ... Progressive ...
As far as the dead hands go, because it begins on the side of my little fingers, he's ruled out carpal tunnel. He's banged my elbows, arms etc and checked out my neck. I now have a prescription for diethylamine salicylate cream and I have to massage it into my elbows 3 times a day. It's an anti inflammatory and he said to stop taking it if I get indigestion or heartburn. If there's no improvement I may have to have conduction tests (??)
The doctor also said if my bg levels began to creep to 40 or 45, I would have to go back to 2 x 500mg. (He said he's scared the nurse will tell him off!!)
His comment about the progressive nature of D has depressed me a little. I always knew it and understood but I was trying to put it to the back of my mind. I really don't want negativity to creep in to my thoughts.
Now I'm going to walk a portion of the 42.
Sorry if I've rambled.
Sent from the Diabetes Forum App
Why feel guilty about the cost, I bet the Doc never feels that way when he gets his 50,000 a year. mine suggestet I should go to the gym each week, well as I am 83 and live on a low pension I wonder where he thinks I can get the money for such things?Sorry for your troubles Hyden and thank you for taking the trouble to read my post and respond.
When I commented about feeling guilty for costing money the doctor brushed it of and said it cost pennies to make millions.
Strange encounter for me that day.
Sent from the Diabetes Forum App
You're very kind. Thank you. My uncle is 81 and goes to the hospital ten miles away, every two weeks, for a blood transfusion. He can drive but is no longer allowed so he is taken. There is a special ambulance - non emergency, and holds a few patients. Is there nothing like this in your area? Or sometimes there are volunteer drivers.Why feel guilty about the cost, I bet the Doc never feels that way when he gets his 50,000 a year. mine suggestet I should go to the gym each week, well as I am 83 and live on a low pension I wonder where he thinks I can get the money for such things?
A big chunk on my income went on a Taxi as I was told not to drive after having the drops in my eyes, Ok it only cost one way as I do have a bus pass
but well 13 pound is a lot. anyone would think we got our meds for nothing, I have worked all my life done two years Natonal service
always payed my taxes and health, I never had a days dole money and in 1982 I got made redundant I did not bother to sign on I went and started to work for my self yes I did window cleaning and progress to becoming a Lanscape gardener.
So why us poor sods with all our allments worry that it cost a few pounds to keep us going am not sure as well when you here this mornings remarks about sacking 8000 guys from the army and then paying others to be trained as part time guys then yes they want 11000 new one but only have got 176, at present, they are offering 7000 a year, So why should we worry, after all we are been told we need to look after ourselves
no carer, I have no Nurse and only see the Doctor as he suggested once evey three months.
No my friend do not worry about what your few tablets cost.
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