Problems months after colon resection surgery: What Helps?
Three months after colon resection I had a severe stomach cramp this morning and have not had a bowel movement yet. This is the first time this has happened. So far things have been good.
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Really so sorry to here you are still in pain and not right yet . But i can just say it has taken me 12months this month to feel 99% normal slowley you will see it getting better , I know surgent or nurses give you no proper information . keep your walks , drink water as much as you can ,, it will get better , but i do hope sooner for you god bless
@riana1 - Welcome to Connect!
Your new pain and discomfort sound a bit worrisome and you should probably check with your doctor.
Hello I just registered and not sure how to navigate site yet. I wish to get feedback on some symptoms I just recently started having. Had bowel surgery due to scar tissue adhesions 11/13/20. I have been taking Linzess and a stool softener to keep things moving along. Years ago I had gastric bypass surgery which I believe caused the adhesions. Anyway I have been able to eat with no problems that is until 1/15/21. All of a sudden my inner stomach feels tender and sore inside as if I just had surgery. Sharp pain in lower left bottom stomach and passing gas doesn’t seem to relieve it. For a couple of days my right side near liver was extremely tender inside and when pressed on. I cannot sleep on my stomach or sides only on my back. Anyway experiencing this?
Just a follow up a week later.. I took someone else's advice and even though my bowel movements are quite regular and of no concern, I decided to add LaxaDay back into my daily routine. I'm happy to say that between that and more water, the gallbladder area pain has reduced to a more tolerable place, so that's great advice for anyone else experiencing that.
This is indeed a new normal. It's very clear that I won't be "bouncing back" anytime soon - this will be a slow, gradual recovery. So glad to be able to read through everyone else's stories so it doesn't feel so lonely and unexpected.
I too had a sigmoidectomy op - 20th November 2020 due to a severe stricture from UC... my recovery has been nothing like I was lead to believe. Prior to surgery I was reasonably fit and was as prepared as I could be for my surgery (in hindsight there was so much information I wasn’t told prior - that I should have been told - eg - nerve endings being damaged / urinary issues / pelvic pain - the list goes on). Follow up post op has been non existent and a joke.. a phone call 6 weeks after. I either have chronic runny stools or constipation, a bloated gut (I could pass for 7 months pregnant) revolting smelling gas which my poor family have to live with - they never complain . All wonderful different sorts of pain - mainly at the resection sight - the pain I have been experiencing the last week is constant and if I stretch or move the wrong way the pain is a 10/10 - takes my breath away. I never know how much pain I am supposed to deal with - what’s normal and what’s not. I have been back to my GP - a couple of times - had a CT scan about 3 weeks ago and everything looked normal - on the outside i suppose. Nothing feels normal - everyday I am anxious and stressed about what the day will bring -how much pain will I have to deal with / will I be near a public toilet / what happens if I need to pass wind (it’s like an explosion - nothing discreet about it) .. I have been walking for about 45 minutes a day - everything I’ve researched has advised to undertake physical activity...I just want my normal life back - none of this is what I expected... 🥲.. I just want a normal bowel motion once a day and to be pain free and not pain every time I am doubled over in pain...this is so frustrating - coming up to 9 weeks post surgery..
Jacob, I believe that 3" incision is where they removed the colon and not for the robotic arm. With the robot OR with regular Lap surgery the scope usually goes through the belly button, which for me was very bruised and still is after 3 months.
Not yet, but I will ask when I next see him. I will say that I increased my water intake to the maximum amount I could tolerate, and that seemed to help (thanks for the tip!) . Also, nearly exactly at the three month mark, my stomach finally released the stiffness it had had since surgery, and I had a few days of it being soft and palpable. I immediately added in exercise probably too quickly, and noticed that on this fourth day it has stiffened again a little bit, but it’s still better than it was. So there’s one story for those searching about how quickly you can expect recovery. In terms of how far along my recovery is, I can walk about one or two miles flat right now (hills continue to slay me), I’m allowed to do five minutes on the bike, and my physiotherapy still looks mostly like stretches. But I’m feeling pretty good.
@cdnmom Welcome to Mayo Clinic Connect. How discouraging to expect a certain time frame for recovery, only to find out that is not the case. You picked a great conversation to be a part of.
Have you asked your physician if they can check for gallstones? They have done studies that show an increase of gallstones and gallbladder disease in patients who have had stomach/intestinal surgeries.
Thank you! That helps a lot. I do have a call into the surgeon for a follow up, but don't expect much more than a 2 minute appointment where he says it's all fine with no explanation. I'll try upping my water and fibre intake to see if it helps. I really appreciate hearing a story of someone ahead on the path. Thanks!
I’m a 45 yr old female and I’m almost 4 months post sigmoidectomy. The best advice I received is that it’s not a linear recovery. I still have pain/setbacks. I’m hoping the 5 month mark is the turning point. I also have “pulling” pain as well as sharp pains and some nerve damage. It’s my understanding that all this can be normal but certainly speak with your physician. What has helped me the most is staying on a routine with - tons of water, kefir, fiber supplement, stool softener and peppermint tea. Certain foods still put me in agony so I take note of that when I try new things. I’m also pretty distended still - that is the worst part for me and I’ve not figured out how to solve that issue. This group has really helped me through this unexpected lengthy recovery - I hope you find some answers. Hang in there!!!