wiserkurtious
Well-Known Member
- Messages
- 368
- Location
- hull
- Type of diabetes
- Type 1
- Treatment type
- Insulin
- Dislikes
- diabetes :P having to eat food in moderation
I'd look for a new doctor, if I were you.
I'd also ask for copies of your medical records from the hospital and the GP, including blood test results, so you can find out what the story is with your kidneys, and check that everything has been thoroughly investigated.
I'm not sure it's possible to lose iron by running. Usually you either have to donate blood, have surgery, or have an injury where you lose blood. (Women lose iron with menstruation and pregnancy).[/QUOTE
Not going to lie, this sounds pretty standard. Type 1 is not easy to diagnose as in the symptoms can be a bucket load of things. Sounds like your Dr was following procedure to me.
Whenever i get blood work done i always ask for a full copy for my own records. It makes it easier to thoroughly go through each item tested and ensure that I understand what the test was, why they did it, and what the results indicated. The internet is fantastic for allowing me to understand everything. I advise everyone to do the same.
As for borderline Anemia and Kidneys - I find some doctors like to give people the 'kidney damage, eye damage, numb feet' speech with the hopes that it scares us into managing better. It doesn't mean they know nothing, it just means they don't know how to communicate what they know to you specifically. I would find a new Doctor if you are finding them hard to talk to about your concerns or if they do not seem to listen to you well enough.
My doctor is all business, and focus mainly on avoiding complications and as such she speaks about complications frequently and has VERY strict goals for me, that seem a bit unrealistic lol but you gotta aim for perfection everyday right, i mean why try if you aren't going to try hard?
Yeah, it's just medical paternalism, the belief that Doctor Knows Best and patients are like children - they are better not to be troubled with things like their medical records. I don't know what sort of patient advocacy/rights organisations and laws you have in the UK, but in NZ, doctors, nurses and receptionists all know that they must provide records on request or else they will be in legal trouble.Hi CatLady and everyone. When I was diagnosed (20 years ago T2) it took 3 years of going to the surgery where the docs said my symptoms were just signs of aging. Booked in to see the nurse for a Well Man Check, and bingo. Generally I've found that practice/prescribing nurses are much more "with it" than GPs. Now on insulin, my current GP practice won't print out blood results - "imagine the cost if we had to give everyone a sheet of A4"!! I've offered to take them in a ream of paper each time - but then they say "but what about the toner costs?". Doh! So email it? "no we are not allowed to email patients". A friend of mine was recently called in for an annual review - she said her GP was "so caring" till I told her how much they got paid for ticking that annual review box. Good luck!!!
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