I was told that as there are no nerve endings, I wouldn't be able to tell when my stoma was active. I can't always, but at other times I have a feeling of pressure that is uncomfortable and sometimes borderline painful, and sure enough my stoma is outputting. My abdomen is also 'harder' at the top of the stoma and there's often a sense of drag. The stoma nurse didn't seem to think there was a problem with a hernia. Do any of you get sensations when your stoma is working? Is that dragging sense something that will pass, or do I need to be thinking about a belt or something to support the bag? Am trying with the pocket inside briefs but haven't found the right fit yet. Any and all advice/ feedback gratefully received :)
Hi Elle55a30c and welcome to the group.
I’m not sure what type of stoma you have, but I have a urostomy and a colostomy. I can feel when the colostomy is working usually, and sometimes it can feel quite uncomfortable just before it “goes”. I’ve always put that down to the normal contractions there just before the output is coming out.
I’ve never had a hernia, so I don’t know what that would feel like but I don’t have any hardness in my abdomen. In terms of support belts, I personally don’t use them, but hopefully others who do can advise on them.
I also just wear normal underwear with no pockets inside-I’ve had 2 stomas for 5.5 years now, and I like to have some normality with my underwear! I’ve never worn any specialist stoma underwear or swimwear as for me I don’t feel that’s needed for me but lots in the group do so you should get some helpful replies about this.
I see from another post you are not long out from surgery, so I hope your recovery is going well. It takes a while for things to settle down, and for you get used to the new sensations but everything becomes second nature with a bit of practice!
Sarah xx
Hi, and thank you for the reply :) It's good to know it's not strange that I can feel my stoma working - colostomy. It is early days, and the stoma nurse is due back Monday so I'll raise the issue about the hardness just above the stoma again. I'm probably just super concerned about getting a hernia.
Developing a hernia was quite a fear for me too in the early days, especially with 2 stomas. I think it’s quite natural. Just be careful in your recovery as regards lifting and don’t try to do too much too soon as you’ll have healing going on inside and that takes a bit of time.
Nowadays, the thought of getting a hernia isn’t on my mind at all. I’ve become used to being careful over the years with things like lifting so I don’t think about it, but in the early days when everything is new we tend to worry more.
I found my stoma nurse in the Community invaluable when I was discharged, so do share any concerns with her-I found mine great for advice and support.
Sarah xx
Thank you - that's reassuring. The being careful about lifting is hard to get used to - husband is basically following me round saying "I don't think you should be about to lift that!", with me going "Oh, it's only - nah, you're probably right!" ;). I think the stoma nurse is bringing some abdominal exercises with her next visit, so there's that :)
Hi Elle
Wise SarahH21 has given you some excellent advice.
I would echo, I can feel when my colostomy is going to work (weirdly never felt my temporary illeostomies, but do feel the colostomy).
I have also been scared of hernias. My surgeon said to me don't do something that increases the pressure in your abdomen - ie lifting heavy things, and for example standing and pushing weights above your head. I've found walking has been a good very gentle way to recover the abdomen from surgery.
Good to hear your stoma nurse might give you some exercises. I didn't get anything useful from my lot, so I used a book called "The Bowel Cancer Recovery Toolkit" as a guide for some staged, gentle core exercises. The book is written by a physiotherapist who has a stoma. She also has a website and offers 1:1 pilates rehabilitation sessions if you fancy that, just google her name.
All the best.
Hi Babotie :) Thank you for the response and for the link - will def have a look at that. I'm starting with gentle walking - was up and about in the ward corridors and am now walking with husband and dog at least once a day (not walking the dog myself as stoma nurses said a hard no to that!) I had to go into my GPs the day after discharge to get some stitches removed, and then a few days later to get a flu jab, so I've had to be out and about, which is a good thing (even if not always feeling like it!)
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