Problems months after colon resection surgery: What Helps?

Posted by joyce1 @joyce1, Feb 25, 2017

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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Profile picture for jacob73 @jacob73

I never was offended mate👌🏼. I'm sarcastic myself, it's in my blood I'm English and Jewish. No other way to be I reckon🤣👍🏻.

So I'm 6 days post-OP let me ask you this...how many pain pills is okay to take? My doc upped my dosage from 1 Norco every 4 hours to 2 every four hours. I haven't had any today as I think it slowed my bowels. I went this morning but, there was only about two fists full of poo. That said, all I had was soup, half a slice white bread and one egg. Up until yesterday morning i was going all the time, albeit only a small amount, but at least 7x a day. I understand this is called clumping. One goes a massive amount and then things slow down. Tonight I'm having sponge cake with cooked cinnamon apples. Not sure what else I'll eat to be honest. The pain gets worse as the day progresses. I don't have UC, or Crohn's, or IBD, however I was mostly constipated until 24, then it became 50% constipation, 50% diarrhoea. Might have to ask my GI doc about Linzess. I don't want to do Miralax every bloody day.

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I went home with a bacterial infection which was not addressed until Jsnuary, 2020; my bowels were all messed up. I think someone else might be able to give you a more straight forward answer. My diet was pretty limited (in my choices). I did incorporate apple slices for fiber and juggled back and forth between adding bulk and fiber to foods that would not irritate causing loose stools. I still eat later in the day. 2:30-3:00 pm, so I can pass my stool early evening. I choose todo this eating schedule so I can make appointments during the day and exercise (on treadmill right now! Multitasking!!!). Took me awhile to figure it out, but I’m sure, in time, you will be good to ago. I hope you get other members responding with helpful advice. Take care

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Profile picture for lisag03 @lisag03

I had my sigmoid (and some other parts) removed via open surgery on 5/6/19. Since then, I developed an anastomtic leak (5/16) SBO (8/19 caused by adhesions—this was resolved with laparoscopic surgery) and had another bowel resection on 11/6 after I had a bowel perforation. This was caused by an unconfirmed entrocutaneous fistula. I developed sepsis as the result of another leak and was hospitalized for five weeks. In my experience, it has taken a lot of adjustment, and my digestion still isn’t normal. Part of this is because I underwent chemo which caused some digestive issues, but stopped chemo in 8/19. I am still struggling with bouts of painful
Constipation. It makes me fearful of another obstruction. I think a lot of it has to do with what I eat because I’m typically a healthy eater and a lot of healthy foods are troublesome. My nutritionist said to take 1/2 to 1 dose of miralax daily if needed. I have a lot of bloating after eating and I’m guessing this may be my new normal. Drink a lot of fluid and try the miralax. If you have other specific questions I will be happy to answer

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Jesus mate, I'm very sorry you've been through all that! May I ask your age? That's quite a lot if sh*te to go wrong with repeated surgeries. What caused the leak? How did they address it? According to my doc that is something I don't need to concern myself with as I've never had any type of abdominal surgery.

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I had my sigmoid (and some other parts) removed via open surgery on 5/6/19. Since then, I developed an anastomtic leak (5/16) SBO (8/19 caused by adhesions—this was resolved with laparoscopic surgery) and had another bowel resection on 11/6 after I had a bowel perforation. This was caused by an unconfirmed entrocutaneous fistula. I developed sepsis as the result of another leak and was hospitalized for five weeks. In my experience, it has taken a lot of adjustment, and my digestion still isn’t normal. Part of this is because I underwent chemo which caused some digestive issues, but stopped chemo in 8/19. I am still struggling with bouts of painful
Constipation. It makes me fearful of another obstruction. I think a lot of it has to do with what I eat because I’m typically a healthy eater and a lot of healthy foods are troublesome. My nutritionist said to take 1/2 to 1 dose of miralax daily if needed. I have a lot of bloating after eating and I’m guessing this may be my new normal. Drink a lot of fluid and try the miralax. If you have other specific questions I will be happy to answer

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Profile picture for virgo1952 @virgo1952

I guess I need to tone it down. It’s partly my (attempted) dry humor. No harm, I hope. Law, me too. Not a lawyer, paralegal then on to further education in business and psychology. Kind of an odd combination but like u (in a way). I left the business side of a hospital and became a patient advocate. Worked with geriatrics mainly. Know enough to hold a conversation at a cocktail party but not a expert by any means. I’m glad you are cheeky! I apologize about the misdiagnosis, no excuse for that. I hope you will accept my apology 😳

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I never was offended mate👌🏼. I'm sarcastic myself, it's in my blood I'm English and Jewish. No other way to be I reckon🤣👍🏻.

So I'm 6 days post-OP let me ask you this...how many pain pills is okay to take? My doc upped my dosage from 1 Norco every 4 hours to 2 every four hours. I haven't had any today as I think it slowed my bowels. I went this morning but, there was only about two fists full of poo. That said, all I had was soup, half a slice white bread and one egg. Up until yesterday morning i was going all the time, albeit only a small amount, but at least 7x a day. I understand this is called clumping. One goes a massive amount and then things slow down. Tonight I'm having sponge cake with cooked cinnamon apples. Not sure what else I'll eat to be honest. The pain gets worse as the day progresses. I don't have UC, or Crohn's, or IBD, however I was mostly constipated until 24, then it became 50% constipation, 50% diarrhoea. Might have to ask my GI doc about Linzess. I don't want to do Miralax every bloody day.

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I guess I need to tone it down. It’s partly my (attempted) dry humor. No harm, I hope. Law, me too. Not a lawyer, paralegal then on to further education in business and psychology. Kind of an odd combination but like u (in a way). I left the business side of a hospital and became a patient advocate. Worked with geriatrics mainly. Know enough to hold a conversation at a cocktail party but not a expert by any means. I’m glad you are cheeky! I apologize about the misdiagnosis, no excuse for that. I hope you will accept my apology 😳

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I'm an AML Leukeamia survivor mate. My oncologist sent me to a colorectal oncologist. So perhaps they wanted to be *uber careful. And, I'm definitely still feeling like sh*te. I just think things can be smoother for patients. I understand the lingo fine. In fact, I practiced law for a decade, got I'll went back to university in order to go to medical school in my mid 40's. I'll be taking the MCAT this June. I hope to be a patients advocate when I'm done. My medical history is riddled with physicians that could care less. So, yes I'm a cheeky b*stard😆.

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It’s the medical lingo. That’s the area where my re-section was performed. I had enough of my sigmoid to re-attach and I didnot require a colostomy bag. Also checked my lymph nodes for cancer and they were clear. Your inflammation and pockets caused damage (I’m assuming) and that is why you had a re-section. Different situations, but same approach. Mine to stop the spread of cancer and yours(?) due to damage. I guessing from what you have shared. Get out your dictionary and learn some new words!!! It’s a language in the medical world. You must be feeling better,. getting feisty???? It can frustrating.

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Here's an odd tidbit...I had a Robotic Xi sigmoidectomy, however on the hospital release info it says "LAR" Lower Anterior Resection. To my knowledge none of my rectum was removed, only my entire Sigmoid and about 3 inches of my descending colon. Why can't things just be straight forward🤬???

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Profile picture for Kanaaz Pereira, Connect Moderator @kanaazpereira

Thanks for sharing your insights, @virgo1952. It is so helpful to hear from others who’ve been there.

Welcome to Connect, @jacob73. I'd like to bring fellow members @sundance6 @corn50 @bamagirlxyz @1943 @rdmishio @mosito @wibly @lisag03 @jmccabe51 @adrianspa @readingteacher and others into this discussion as they have experiences with the recovery after sigmoid colon resection or that of a loved one. You may also be interested in reading this discussion that talks about some of the issues you're experiencing

– Sigmoid colon resection: What to expect for recovery? https://connect.mayoclinic.org/discussion/sigmoid-colon-resection-10282019/

With regard to the incision, have you spoken to a wound specialist, @jacob73?

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I remember asking similar questions of others. Joined the Digestive Health group too, when I was diagnosed with c-diff. That was helpful also. It’s very confusing and scary for many reasons. The medical world has changed. Better care in many ways, but I think information is limited and/or can be censored. Fear of legal responsibility. You have to be informed. Ask questions. Be ready to “rock” the boat if necessary. sasha

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Thanks for sharing your insights, @virgo1952. It is so helpful to hear from others who’ve been there.

Welcome to Connect, @jacob73. I'd like to bring fellow members @sundance6 @corn50 @bamagirlxyz @1943 @rdmishio @mosito @wibly @lisag03 @jmccabe51 @adrianspa @readingteacher and others into this discussion as they have experiences with the recovery after sigmoid colon resection or that of a loved one. You may also be interested in reading this discussion that talks about some of the issues you're experiencing

– Sigmoid colon resection: What to expect for recovery? https://connect.mayoclinic.org/discussion/sigmoid-colon-resection-10282019/

With regard to the incision, have you spoken to a wound specialist, @jacob73?

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