If I couldn't manage acceptable control on MDI (and I appreciate I'm lucky I can, or perhaps it's because I work quite hard at it) and had to use a pump, it really would curtail my activities.
Oi Bev, don't go twisting my words into pro-pumping 😉 😛
Oi Bev, don't go twisting my words into pro-pumping 😉 😛
He he - why Katie - are you thinking about a pump?Bev
Hahaha I don't think Bev meant to twist it. I actually read both your posts to mean the same anyway 😉
I do agree though and I'm not saying this about Copepod necessarily.
There are people on the cwd list who have this great control but don't carb count, don't have hypos or hypers and the rest of us just think, how the hell is this possible as we work our butts off trying to get a small semblance of control.
It just boils down to luck of the draw really and how your body is made up. For some people, although they do work hard, the same as some of the rest of us, their HbA1c will always be better because overall they have better numbers and I think that this is down to a bit of luck in as much as their diabetes behaves itself.
Don't get me wrong luck is not normally a word I would associate with diabetes and it is all pants but I think you get my drift, well hope you do. 🙂
Fortunately my French doc is allowed to prescibe a pump for too many hypos even if the Hb A1c is well within targets.
For what it's worth Copepod, I read a blog article by a crazily active mountain-climbing T1 who was returning to MDI from pumping as he found his pump was too much bother in the wild. (OK, OK not that it would be for everyone pumpers!)
I thought the point about being able to change basals at any time was a very good one. Having said that though, with all your insulin eggs in one basket, a kinked cannula/duff infusion site could send you into hyper meltdown halfway up a cliff.
I love too that pumpers are being honest about the amount of work and care required to pump effectively.
What is clear to me from this discussion is that they are both far from perfect systems (though pumping may just have the edge). Each have very particular pros and cons, and that we need to find the one that works best for us at whatever period of life we find ourselves.
The only time I've seen an insulin pump in action, it was attached to a Mountains for Active Diabetics member, when we were both changing into posh clothes for a DUK award ceremony - she seemed to be having lots of bother fitting it inside her dress.
I also worry about the "having all insulin eggs in one basket" aspect - that would have been disastrous in my recent 48 hours (very) wild camping staffing an abseil section of 4 day & night adventure race.
I'm sure pumps are right for the people who have them (and their parent), but I wouldn't want to be forced to have one, and am very appreciative that my situation (whether luck / genetics / self management) means I find MDI more suitable.
Hiya everyone,i have been referred to go on a pump and cant decide if i want to or not.I would like the people who are using a pump to say if they are better now they are pumping or were they better controlled before pumping,and any advice on pumping would be helpful.I dont see DSN until 13 sep and she is going to give me all the literature then,said it was no good giving it to me unless we knew for definate i had been referred.Thanks.