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Pumps - are they uncomfortable?

Sarebear86

Active Member
Messages
35
Location
Letchworth
Type of diabetes
Type 1
Treatment type
Insulin
So I'm considering getting a pump but I'm a little concerned about the tubes and cannula being uncomfortable, especially at night? I also get extremely itchy and achey when I have a cannula in for a drip so am wondering if the pump cannulas feel similar? Any help would be greatly appreciated
 
Depends where you site the cannula really. Most pumps require site changes every 3 days so if you find where you have it to be uncomfortable you'll only have to move it in a day or two anyway, so it's no big deal.

I hate being cannulated in hospital. Having a pump in doesn't feel anything like that for me. I often forget where I've sited my pump and have to give myself a little pat down to find it.

Have look on YouTube for people actually using and placing pumps. Have a little Google for belts and things to wear pumps in to make sure they are nice and comfy and tucked away. It all ends up working fine when you find a way that suits you.
 
@Sarebear86 most of the time I'm completely unaware of it. I wear it in a Hid-in pump belt, and that's very easy to wear, and I rarely feel the cannula. Actually if I DO feel the cannula I assume that it's because it might have an issue so I change it straight away in those (very rare) scenarios.

In bed it's fine - sometimes I have it in my pocket, sometimes in its belt, sometimes just in a sock but 'free range' in the bed if *coughs* it's a warm night.

I borrowed an obsolete pump from my diabetes centre for a couple of weeks, and I test-wore it - I was staggered at how much less of a 'thing' it was than how I'd imagined.

I'd had diabetes for over 29 years before I got my pump. I wish I'd pushed much, much sooner for the opportunity to get one!

 
I forget Ive got mine on most of the time, at first (maybe a day or three) when you first start off on a pump you are constantly checking, but after that its just like its part of you.

Unlike @Snapsy I only have warm nights during the summer hahaha
 
Sarebear86 said:
So I'm considering getting a pump but I'm a little concerned about the tubes and cannula being uncomfortable, especially at night?
Click to expand...

I'm using a tubeless pump but don't find the Pods uncomfortable at night or during the day, in bed I try not to lay on the side where the pod is placed but apart from that all is good

Sarebear86 said:
also get extremely itchy and achey when I have a cannula in for a drip so am wondering if the pump cannulas feel similar?
Click to expand...

The hospital cannula is inserted into a vein which makes it uncomfortable and itchy, a pump cannula is inserted into the subcutaneous tissue just like on MDI, like the ladies (and Gaz) who have replied above I rarely feel the cannula in my body.
 
Thank you so much for the responses guys! I'm thinking I might as well give it a go especially if it's as easy as everyone says it is
 
Sarebear86 said:
Thank you so much for the responses guys! I'm thinking I might as well give it a go especially if it's as easy as everyone says it is
Click to expand...

Have you actually spoken to your consultant or DSN and been given an indication they would support you having a pump? That's the first step.
 
Sarebear86 said:
They were the ones that suggested it but I was unsure.
Click to expand...
it is some work -- you are needing to test a fair few times a day and your carb counting needs to be pretty spot on too.

I have been on a pump now for 14 months -- ( 44 years as a T1D )
best decision I have made
 
I been pumping for a month now and it is the best thing I have done. So much more control
 
I don't notice my pump at all, and often forget where my cannula is. When I first got my pump, I was aware of it for a couple of days simply because I wasn't used to it, but after that I didn't and don't notice it at all
 
don't notice it at all I've been pumping almost 11 years. Wouldn't give it back in a million years wish I'd gone on it sooner, I've been type 1 for 30 years
 
Although I'm not yet on a pump (I'm in the process of getting one) i do wear Iports, where the canula sits under the skin and you inject into the iport as I am not that great with injections. I don't feel my cannula at all, I did however after a whole start to itch and panicked thinking I was taking a reaction when Infact I wasn't, but I was given Cavilon. This is a barrier cream you put on prior to putting in the iport (or in your case a pump) and this stopped any itching I had
hope that helps
 

Thanks Laura! I didn't know they could give you anything to help with the itching, that's good to know
 
You can't feel it - I often forget I am wearing it. The part that takes the most getting used to is carrying it around all the time (in pockets, at bedtime etc)
 
It is nothing like the ones in hospital. The ones in your hands? Those hurt like a mf. I'd compare the initial set going in to when you get blood taken at the hospital. But once its in its in. I have my pump in a pouch around my neck at night, or down my bra during the day (they say one boob is always smaller so find that site and throw it in!) so it doesn't bother me but there are a world of options on how to store it to get the best rest you can. Some just shove it under their pillow tho. I don't find it itches, not unless I've left it in too long and need to change it and that just depends on the person. If you heal faster you will need to change faster as your body will try to start expel the site but if you don't you should get 3 days. Heat or cold can cause an itch but nothing too bad.
 
Been on a pump now for 5 weeks..35 years T1D. Resisted the pump for some years but was running out of options with pens so finally took the plunge. Taken a week or so to get levels right and to get use to the presence of it but defiantly the right move.
If you are lucky enough to be offered one go for it, the benefits far out way any of the little problems it may bring.
 
GPs can prescribe a spray to help remove the cannula after.
The cannulas are so tiny. They are minute, nothing like cannulas in veins etc!! If you can feel a cannula, it is a signal that it is not going to be working effectively,so best to change it.
 
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