Mumsnet has not checked the qualifications of anyone posting here. If you have any medical concerns we suggest you consult your GP.
Anyone have experience of a stoma - please help!(49 Posts)
DH had ilisotomy as a result of crohns about 12 weeks ago. Generally going okay, but as had a couple of episodes of stomach upset. During which time he gets severely dehydrated, VERY quickly, making him faint and feeing general crap. Currently having one of these episodes, projectile vomiting, and getting very dehydrated quickly. Anyone have experience of this during the early recovery stages and any tips would be MUCH appreciated !! Thanks...
I had a temporary ileostomy due to Crohns, and I'm actually having surgery at 7am to have a permanent one! I came on err to distract myself and find your post ... Crazy how things work!
Anyway, when I went through this with my temporary one I was told full fat coke and ready salted crisps, the sugar will help with the faint feeling, the salt helps with the absorption of fluids. If it lasts for more than 2 days I'd ring his stoma nurse or go to your GP as he may need fluids, if it gets too bad just go to a&e. I have Crohns though and I understand that sometimes all you need is to sleep, drink and eat what you can and rest without going to every medical professional! Definitely do the coke and crisps thing, and keep an eye on it! Especially the output, if it's significantly reduced just go to a&e as there may be a blockage caused by scar tissue and that needs sorting. Hope he feels better soon!
I just wanted to say hello and that I had a colostomy fitted two weeks ago due to Crohn's disease as well. Hence me being awake at two in the morning. I find I get very thirsty very quickly and have been advised to be constantly drinking. Sometimes I feel miserable although I am aware it's early days. How long have they anticipated recovery to be? I will have to go back to work next month and still feel like I have been hit by a bus (I also had my fifth and ''final' bowel resection
Sorry I haven't been much use. If I have any problems we locally have stoma nurses (linked to hospital) have you got similar? They have been fantastic (have wound infection and stoma problems).
Oh wow snap!! I had a permanent stoma 5 weeks ago and am up late because I'm thirsty and sore as well. It is so reassuring to see other people who have one as sometime you feel so alone. Another chrons person here as well I've been getting very thirsty - I find water with Gatorade in it really helps. Wannabe, I know what you mean about getting back to work. I have to get back soon but just have no clue how I will manage a commute and a 8 hour day as I get tired. Best wishes to you all and as I say, nice to be in contact with others going through this.
Thanks ouch and wannabe for such quick replies!
Output is actually really high, watery, yellow (sorry for details). Has taken some loparomide and we have the full fat coke on the go! He is complaining of stomach pains. And is being sick which is obviously not helping with the dehydration.
Really hope it's just teething problems as we really thought the operation would be the end of the misery this bloody illness brings!!!
Wannabe - his recovery has been pretty good, still very very tired (again is this normal), he was back to work after 6weeks, but out of hospital after one week....
Consultant said recovery could be anything from 6-12 weeks.
Are these episodes are teething problems, a bug picked up, or just life with a stoma? Poor DH, he never moans but I can see he is just fed up with it all.
Ouch - wishing you all the best for your op tomorrow!!
And hello ifyouletme! Thanks for post also! Good luck with the recovery x
Verybusymum I had the same thing recently. Huge amounts of watery output, stomach cramps and really thirsty, extreme nausea. It lasted 24 hours and then I felt much better. How long has your poor dh had it? Any longer than that and i would go to a&e as could be a blockage. Poor thing i feel for him (and for you), its so tough when you just want to be better and feel crap. Has he had any output in his bag or just water?? Could he force down a banana as that helps with potassium and thickening output.
Does he have any anti-sickness medication? I have ondanestron and cyclzine which help! Definitely try eat some solids, just watery is an indication of a blockage too, but as you said there is a lot id be prepared to bet it's just teething problems - but it's always best to be safe!
Thanks for the luck, ill need it, I'm very nervous!
Will be thinking of you Ouch, hope the op today goes smoothly. Have you had to fast and take horrible prep stuff??
No, they do an 'enhanced recovery' thing at my hospital and my surgeon says that prep cause more stress on the patient and bowel before hand - so pleased I got away with it! I've had some carbohydrate drinks which aren't that bad, just a bit sweet, they're meant to help my body recover when I don't eat after the op, so I don't get super skinny!
Well he finally got to sleep. Every time he drank anything it came straight up. So hoping the sleep will do him the world of good and although maybe worn out when he wakes hoping, the pain and watery over frequent output would have settled. He is under such pressure as its our babies 1st bday party on Sunday. I told him it doesn't matter, we can rearrange but he doesn't want to. Typically bad timing!!
He had a blockage before with no output and terrible pain, the culprit a pea! Which he now avoids. I never realised a blockage could result in watery output
Will get him to speak to GP about anti sickness pills, thanks for that idea!!
[Thanks] to you all for advice.
Wishing you luck again with your operation OUCH, you will be in good hand.
And wishing each one of you a very speedy recovery!
We had enhanced recovery at the hospital I was in. I was amazed how quickly they try and turf you after major surgery. I have found it so hard since I have been home. Everything exhausts me and I have been returning to the hospital daily as have an infection in my wound (am on augmentin 675mg four times a day) and the stoma was pulling away from the stomach wall. They are keeping an eye on it. I have no appetite so am losing weight.
I was told to avoid coke due to gas. Does it help then?
Wannabe that sounds so painful you poor thing. I haven't actually tried the coke thing myself but my stoma nurse said if I ever thought I had a blockage to drink a bit as it may help. I sympathise with the no appetite - mine is only coming back now.
Verybusymummy I hope your dh is feeling ok. And that the birthday tomorrow is a happy one. You sound so supportive and amazing, bless your heart.
Take care everyone! Sometimes it feels like two steps forward, one step backwards. But sounds like we are all really early days with our stomas and getting to know what works/doesn't.
Think you can put a bit of sugar in the coke and that makes it flat .
Maybe try rehydration powders like dioralyte ?
Cant believe they sent him home with no antisickness tablets ,well really you need those sublingual ones that just dissolve next to gum as if being sick ,tablets are no good ! .
Buccastem is one I think .
Would it be worth trying to get over the counter ,otherwise A&E or OH GP ?
Sounds awful for all of you .
My colostomy was years ago, and nurse retired soon after, no arrangements made for successor. Colostomy Association's free magazine was a real help, and their system of having trained volunteers available for a chat also very useful, particularly on a bad day.
Best wishes to Ouch for the op, you'll soon get used to changed life with (hopefully) no poo problems.
Just checking in to see how things are. I am seeing the surgeon today in clinic. Am 2 weeks 4 days post op and see feeling rough! I am finding it frustrating. Am so tired but struggle to get comfortable in bed. Eating is still difficult and I just feel fed up generally.
Anyway verybusy wondered how your husband was getting on?
Hi I hope it is OK to join in here, my DP had an ileostomy just over 2 weeks ago for bowel cancer, happily we had the news this week that there is no spread. He has been very unwell and is only now getting his appetite back. We are a bit unsure about his medication, he has run out of Naproxen the anti inflammatory he was prescribed in hospital and we wondered if he still needs to take that? I think it was for the internal bruising after his operation. Also if he is not taking those is it still best to take his antacid (Omeprazole) to avoid getting indigestion/reflux whilst things settle down. Thanks in advance for any replies.
How are you all doing??
fish, I am please you had the news that it has not spread. Hope is continuing to recover well.
Wannabe - sorry to hear you are still feeling unwell and low. How did it go with the surgeon?
DH unfortunately missed our baby's party. He was so ill,he couldn't even manage to get out of bed. And once the vommiting stopped, he was wiped out for another 3-4 days.
In fact, he too is so so so tired all of the time, It's funny because both consultant and GP said once the bowel is removed he would feel a million times better to be rid of it, It seems to not be the case at the moment.
DH is also very fed up at the moment. He is tired, he gets stomach pains and indigestiony pains and the output is quite high. Not really sure how to make him feel better, other than let him rest and take it easy. Is this pain normal and
Can I ask about output?? Since he was unwell, his output is quite high and he is having to empty lots during a 24hr period, particularly at night. Is this normal? And is pain normal too? He drives me mad slightly because he refuses to call up the stoma nurses to get these questions answered!
Oh very that sounds hard .
Could you ring the stoma nurse and have a chat with her ? Or would that upset your DH ?
Hi all. I can't believe the timing of this thread. My df had his bowel removed 3 weeks ago due to bowel cancer and has an ileostomy. He has had some complications with blockages due to scar tissue. He is back in hospital at the moment as he is quite weak. Unfortunately they have found what he calls a trace of cancer in his lymph nodes and is going to start chemo in a few weeks.
He gets a lot of pain when the blockages starts and very little output. He is then very sick and feels better for a day or two then it all starts again.
When I had my illeostomy I always suffered very high, watery output. I found one of the best things was marshmallows and jelly babies, silly as it sounds they really helped to thicken the output up. Also a spoonful of applesauce per day.
I was always told to avoid fizzy drinks but to drink squash / juice (not plain water though as that can dehydrate you).
I was also told to avoid fruit with pips, nuts, peas, sweetcorn as they can cause blockages.
Good luck everyone and hope those of you struggling are feeling a bit better now x x
Do you mean apple sauce from the jar that you have with a roast?
Well we are up again tonight, he has indigestion type pains all over. In his back, chest, stomach cramps which come and go - is this Normal??
It's not is it?
I am making an appointment with GP tomorrow for him, no arguments
My mum had a colostomy and had to avoid peas like the plague, they were terrible. When she started bringing food up again, it usually meant a blockage, so if he's still having problems, definitely get him to the doctor or hospital.
As an aside, if you add water to any fizzy drink, it usually knocks the fizz out of it - the more water you add, the less fizzy it becomes. I (and Mum) used to drink flat ginger ale for nausea, but coke would work too (we just didn't like coke) and coke would help to digest/dissolve whatever is causing the problem, if it's food.
Good luck - hope it's easily fixed.
very no that doesn't sound right . Is he on anything for indigestion ,like omneprazole ( sp? )? sorry if you've already covered that .
Is there someone with specialist knowledge you could contact - have you got any numbers to ring about this type of thing ? Can you ring the ward he was treated on ?
I know it can be hard to get through sometimes - I phoned the Macmillan people at the hospital once and they contacted the specialist nurse for me and got her to ring me . The MacMillan person has an answer phone if they're not there but they're very good at phoning back .
It just seems so wrong that you're left struggling to cope with this on your own . And unless your GP is really good I worry that they won't know much and will just refer you back to hospital . Though maybe they could ring on your behalf .
Good luck ,let us know how it goes .
Join the discussion
Please login first.