Reversal Surgery

I had an ileostomy reversal surgery in June and by mid July I was able to return to work.  I stayed 4 days in the hospital.   My previous surgery (in April) was removal of my large intestine along with the rectum (and tumor) and removal of part of my small intestine due to an infiltrating mesh.

Kathy

Rebecca:

This is my story.  Hope it provides some insight.

Background: I was diagnosed with rectal cancer in May 2017 (stage II clinical).  In July and August 2017 I underwent 25 sessions of radiation while taking Xeloda.  CT scan in September 2017 showed complete eradication of tumor.  Resection surgery was performed in October 2017 and a temporary ileostomy was created to allow my rectum more time to heal.  Pathological staging was reduced to TONOMO.  In November 2017 I agreed to adjuvant chemo (FOLFOX6) but only completed three sessions before I stopped due to the detrimental effects.  Another CT scan was conducted in March 2018 and indicated NED.  On March 26, 2018 I underwent surgery to remove my port and to reverse my ileostomy.

My surgery lasted about two hours and was without any complications.  However, I remained in recovery for an additional two hours because we could not get my pain under control.  Once I was rolled to my room I began to relax and finally my pain relented.  No catheter.  I had an IV and a PCA.  My diet was clear liquids only.  At this time we were monitoring for any issues from the surgery and anxiously awaiting the awakening of my bowels.  No issues during the night except for insomnia.

Tuesday (day after surgery) was the beginning of the increase in my intestinal discomfort.  By afternoon I was definitely feeling some cramping.  My appetite, even for liquids, began to wane.  During that night the intestinal discomfort turned into pain.

Wednesday was my worse pain day.  I would alternate between moments of relative rest separated by increasingly expanding episodes of very painful cramping.  That is when I began to vomit.  Oh boy, did that ever hurt!  I never developed any fever but I alternated between hot flashes and chills.  Miserable.  Finally, at 1 a.m. on Thursday morning I experienced my first BM.  I was so happy because it began the process of pressure relief in my bowels.  Those trips to the toilet occurred every 90 minutes until early morning.

Thursday was not as painful as Wednesday, but I still had my moments.  I was walking more frequently and for longer duration throughout the day.  I also sat on the toilet several times through the day (probably 10) and was evacuating nothing but clear liquids or slightly brown liquids.  Nothing anywhere close to a formed stool.  I tried to convince the surgeon to discharge me.  He knew best and I stayed one more night.

Friday was my day to leave the hospital.  I felt so much better and knew that my condition would improve and the healing process accelerate once I got home.  I was successful in getting their permission to leave the hospital on my own - no wheelchair.  I was motivated to put distance between me and the hospital!  When I got home I took a long nap.  As is my nature, I wanted to test my abilities so early that evening I drove myself to a Kroger (one minute drive) and bought some food items that I thought I would need.  I did this also to see if I could do it.  It was a success.  I did not poop in my pants.

Saturday and Sunday were similar days of recovery.  For whatever reason, my bowels seem to be more active at night so my sleep (at night) has been even more disrupted than it was with the ileostomy.  On average, I was making three trips to the toilet each night.  Through the days it was about 10 times.  Gas seemed to be the greatest culprit because it significantly increased the sense of urgency.

Overall, I am so happy to no longer share my life with an ileostomy.  In the meantime, I am defining my new normal and learning how to manage it.  By the way, after a few days of carefully selecting items to include in my diet, I said to heck with it and ate some corn on the cob and a fresh salad.  It was wonderful and did not cause me any intestinal distress.

Jim

Hi All,

I am new to the site and full of questions. I 73 years old am T3c N1 M0. I am on a short course of neoadjuvant therapy with plans for a surgical resection. Radiation done, just finished my 6th of 8 cycles of FOLFOX, so far AEs are manageable, terrible taste is bothering me the most right now, neuropathy starting to kick in Fatigue kicks in on Day 5-7 of my cycle and then I seem to bounce until the next Cycle. I continue to work, I travel once a month, and work from home. The next steps are the most worrisome - the thought of an ileostomy sounds terrifying, the surgeon says it would be in place 6-8 weeks, that even sounds long. I read about other options, but guess I need to explore the second opinion route and find someone/where who does the Laparoscopic resection to see if I would even be a candidate. Why do such a big surgery when there is an alternative to an open resection, leaving me with a ileostomy. Then there is the question if the tumor is no longer visible why not watch and wait. so many questions, anyone out there with any experience with this??

That is great to hear, how long did you have to have the ileostomy?

Best wishes for a great 2022! Sounds like you beat it!