rockape37
Well-Known Member
- Messages
- 351
- Location
- Kettering, Northamptonshire
- Type of diabetes
- Type 1
- Treatment type
- Pump
- Dislikes
- Over the top political correctness
I and i dare say I'm not alone am thinking of using a pump pouch. What i would like to know is how people wear them including pros and cons both from a Male prospective and Female prospective.
I'm in favour of the Hid in multiway type your views please.
Regards
Martin
For me a pouch is merely for comfort of wearing the pump and also access. At the moment i wear mine around my neck on an Id card lanyard, it serves it's purpose but can be annoying when it moves around and gets twisted and somtimes ends up upside down.It's an interesting discussion really. If I was using a pump without the CGM link up, I'd go for a patch pump, as I don't see any benefit to a tubed pump that needs to be hidden away and therefore having to wear something (that to me is) relatively uncomfortable to hide it.
This is how I feel too. I wear my pump in a pouch out of the way not to have it hidden, but to be able to wear it really comfortably somewhere where it means I'm not having to, say, yank it out of my pocket whenever I need to have a wee and in so doing potentially getting myself tangled up or dropping it. For me in the daytime this means anywhere above trouser top level, in a Hid-in. At night I either sling it in my much looser Spibelt or just have it free range.For me a pouch is merely for comfort of wearing the pump and also access.
A pouch for me means stability and not a means to hide it away.
I have never hidden myself away taking injections and won't do tge same when i have to check my pump or enter a carb value etc.
It would be nice if i could do things remotely with the 640, but then its still a lot less hassel using pens etc in my opinon and better BG control.This is how I feel too. I wear my pump in a pouch out of the way not to have it hidden, but to be able to wear it really comfortably somewhere where it means I'm not having to, say, yank it out of my pocket whenever I need to have a wee and in so doing potentially getting myself tangled up or dropping it. For me in the daytime this means anywhere above trouser top level, in a Hid-in. At night I either sling it in my much looser Spibelt or just have it free range.
I count myself very lucky to have an Insight, which means I don't actually have to access the pump itself to tell it to do something. I do do some things straight on the pump, sometimes - for instance today I'm at home poorly and am twiddling with elevated basal rates due to this infection, and I can easily get to it to press a few buttons and sort that out, especially if I'm under a blanket on the sofa and can't be faffed with reaching my arm out to grab the handset.
Given that I don't ever eat anything without testing first, which is something done on the handset, I always do the bolus calculation on the handset, and insulin delivery therefore also with the handset. Pump stays pouched-up and cosy, no fiddling, happy Snapsy.
I am finding, as time goes on (10 months pumping next week!) that more and more I've got the confidence to use either 'half' of the system. But I'm so glad I have the option to do this stuff remotely.
Thanks Martin - and I'm only so in love with my pump because it's my first, so I have no experience of others and their own individual and different features (although today's news about the Medtronic MiniMed applying to be licensed by the FDA in the States might well sway my 'wannabe' allegiance in the future!).
Not dissing any variations of this fabulous kit of ours - they are all different, as indeed are we! Take my Insight fanfare with a pinch of salt - I'm just a very keen newbie happy with a new toy. Hope I haven't caused any offence.
And I share your view that pumping is less hassle than pens - and hypos for me now are a rarity, because on MDI I was using far too much insulin. I love not having to eat ALL the time - I think that's my biggest bonus with pumping.
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