Sigmoid colon resection: What to expect for recovery?
It’s been 4+weeks since my resection. Found a cancerous polyp during a routine screening. Some frustration over the lack of information given by the surgeon as to what to expect afterwards. Late 60’s so I know the healing will take time. Mostly, struggling with bowel urgency/frequency and experiencing stomach pain from gas (pretty sure) is three months s realistic time frame for returning to “normal”? I’ve seen some posts that talk about two years? No further treatment so I was lucky. If anyone has had this surgery and went through or is going through the healing process, I would love to hear from you. Just kind of out there.
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15 years ago I had a so-called “Dukes B” colon resection for a cancerous polyp which protruded partially through the colon wall but did not reach the nearby lymph nodes.
Post surgery radiation following this and a subsequent radical prostate surgery were deliberately delayed 5 years so as not to inflame a previously long existing hemorrhoidal pain or irritation condition. Unfortunately, a 5 year delay only postponed that daily discomfort from which I still suffer daily. Earlier hemorrhoidal removal surgery might have been a good idea and long term fix, but I am now 86 and resist all and any elective surgery. Consult your doctor if this condition applies to you.
That is great to hear you have recovered relatively well. I bet pickle ball helps you as well. We are looking into that as well.
I had an emergency open colon resection early September 2021 due to a twisted colon. They removed 18". I had been experiencing on and off extreme pain for a while. I am 70. Spent 11 days in the hospital. I was back to playing pickleball 5 weeks after going home. Still taking ducolax and miralax daily, but otherwise doing very well. I too have about a 6" vertical scar.
The hernias were from having so many open abdominal surgeries in a short time. It weakened the abdominal wall. My second surgery required a wound vac and therefore, the wound wasn’t sutured outside. My third surgery was laparoscopic but I developed a fistula. My fourth surgery was open as well and the umbilical hernia was most noticeable. I also ended up having diastasis recti as well as the umbilical hernia and two others. I just had surgery in June to repair them all and they repaired everything including the muscle separation. It is called component separation surgery. I had a few complications, including discovering I’m now allergic to contrast, but am back to running and barre classes
Best of luck to you!!!
I'm having a LAR October 4 and there will be uro-gynecologist there to put stents in my ureters.
Yes. I go back to the Urologist in 6 weeks and have a handful of questions for him.
Was wondering if other folks who had a robotic sigmoidectomy had a Urologist put stents in bladder parts as a precaution?
What caused the hernias?
How exactly did they find your tumor in your bladder? Was it when they went in to put the stents in your ureters for the surgery?
John, ask about an oncology dietitian at your cancer center. They may have one. My dad was referred to one after his colon surgery. It was helpful.