At least 8 times a day imho, plus a few night time tests.I didn't mean it like that, I have been testing more, it's just everyone I ask about the pump it's always the same answer that I'm not testing enough, there's some days I'm testing 7-8 times a day, how many times do I need to do it?
I can't get my head around why people would actually want something **** near permanently attached to them if they (like you) could get improved bloods from giving mdi.
If after trying to do blood tests and amending doses etc that reasonable control is not gained. Then it is perfectly reasonable to request a pump.
Just that there seems to more people wanting a permanent gadget attached to themselves without really tring to make the efforts with control using mdi.
It just scares me that people seem to think that pumps are an easy option without the full realisation that the management of them is more effort, testing is more frequent and DKA is possible from set failures etc.
I am eternally grateful that I have a pump, but it just worries me that if effort can't be made to inject and test on mdi then why should people expect to just get a pump, when others have made huge attempts to gain control and still can't gain good levels. Postcode lotteries still apply as well.
You shouldn't fear that you will offend anyone. We're all entitled to our opinions.PS DON'T WANT TO OFFEND ANYONE AND SORRY IF IT DONT MAKE SENSE LOL
You shouldn't fear that you will offend anyone. We're all entitled to our opinions.
This thread holds a lot of negative posts. All people need to remember is that people can change. Everyone should be able to get the best care possible.
lol definitely. Never hide what you think. Low blood sugars certainly allow us to speak our mindsExactly my point lol just had to get it off my chest and well you know the saying "drunken minds leads to the truth" or whatever maybe thats the case when you're hypo lmao!! x
In some aspects I agree, but the basics do need to be grasped ie carb counting and the ability and wanting to take control and manage your own health. It is not just a nice new electronic gadget to have.
The NHS has not got enough staff to give endless assistance to people on pumps. People have to have the attitude that they can manage a pump themselves and to do it.
There was a poster on here a while back that was having the threat of there pump funding stopped and having to give the pump given back, I can't recall what the final outcome was though.
Hi Kevin, if you didn't have doubts this wouldn't be normalI have been considering trying to get a pump or at least try for the last year or so and on a recent appointment with my diabetic specialist nurse she said I would be a candidate but there are some things that I still worry about and I am still in two minds. When you got one did you have doubts or were you 100%? I'm not a new diabetic I have been one for the last 16 years from the ago of 11
The pumps most people use have tubing which comes in different lengths and even though this may seem strange after being on injections for about 44 years it took less than 4 hours to get used to the tube. In fact I kept checking to make sure it was still thereThe management side of it isn't the bit that scares me as I already spend a lot of time and effort trying already it's having the device physically on my all the time that I'm worried about. Things like when sleeping or getting intimate with someone etc. what pumps do people have?
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