It’s over. And it’s just begun.
The surgery is in the past and it went really well. The doctor told us that everything went as planned and they were even able to take my colon out through the ostomy which means they did not have to make another incision for it. However, he did say that, by the looks of my colon, this was the right decision to have it taken out. He also confirmed that I definitely have Crohn’s Disease (and not Ulcerative Colitis) and will not be a candidate for a j-pouch or possible ostomy reversal in the future. In all honesty, I wasn’t counting on that as an option to begin with.
But now, I’m having to move on post-colon. Following surgery, I spent pretty much the whole day in the recovery area waiting for a room. My family and friends were able to come back and see me for a few minutes here and there, but I slept most of the time. It was about 7 p.m. before I was moved into a room. By this time I was feeling alright, just very sore and not able to move much. I’m also hooked up to a bunch of different lines, so moving around is logistically difficult as well.
Overnight was interesting. I won’t get into it, but let’s just say that I am not a fan of semi-private rooms. I don’t think I slept for more than a half-hour at a time the whole night.
Today I’m still dealing with pain and being tired, but it’s been more manageable that I thought. I don’t like the whole not being able to get up and move around when I want to. And not having been to the bathroom in two days is bizarre! I haven’t quite wrapped my head around that, yet.
I met with the ostomy nurses today and they began showing me how to take care of my ostomy. (I also found out that I have been slightly mistaken with my terminology. I actually have an ileostomy, rather than a colostomy, since none of my large intestine is left.) They walked me through cleaning the stoma and changing the bag. This was the part of the day that was the most difficult. Really seeing it for the first time, I think the reality of it hit me. This is going to take some getting used to, and there are going to be times where I’m going to have a difficult time accepting it. I still know this was the right thing, but actually coming face-to-face with it was overwhelming. I’m doing better now, though.
My next steps include getting back some mobility, learning more about the ostomy care and pain control. Also, the clear liquid diet has got to go! Hopefully moving onto something solid in the morning.
I think that about covers it. I wanted to give everyone an update and give one more big Thank You for all of your love, support and prayers. They have been paying off!

7 Comments
Praying praying praying! Love you lots! You are such a champ for doing this Steph! Stick with it – I am so proud of you and excited for you to get your life back!
May 8, 2012 at 6:49 pmThanks, beautiful. Y’all’s support has meant a lot. Love ya!
May 9, 2012 at 8:34 pmHey Stephanie! Good luck and I hope everything works out for you. Keep us updated on how you get situated with the stoma.
November 25, 2014 at 1:53 amJust realized this is a really old post. Sorry about that 🙂
November 25, 2014 at 1:54 amHello,
April 30, 2015 at 2:17 pmThank you so much for having this website. It is helping me understand more about Ostomies. I have just suffered my 5th attack of diverticulitis. I have been turned down for surgery by 3 different surgeons already. They say there is a 90% chance I will end up with a bag if I make it through the surgery. I have no small intestine already so it would be permanent.
There is an alternative, and that is for them not to do the surgery and make a small incision and just give me the bag. If I don’t do the surgery each attack will get worse until they have no choice to do it as an emergency.
After reading all your information, I’m going to go back to the surgeon who said (only one out of 3) he would make a small incision and put in the bag.
Can you give me any before hand advice? Any information would be greatly appreciated.
Thank you,
Tina
My name is Janet and my story is a little different. I had a neurogenic bladder for the last 18 years and over time my condition became really bad with incontinence. I had multiple surgeries and had control for about 7 years and then things became progressively worse where my anal sphincter went and my colon died and I had no motility. Needless to say my surgeon took out 1/2 my colon at my request because I was so young and I wanted to make certain that just because my left colon didn’t work, how did he know that the right didn’t. Well they ended up having to go in again, take the other 1/2 of my colon and do a bladder augmentation simultaneously. Now I have a permanent ileostomy and have to Catherine to see through my belly button. I have lost 72 lbs. And am struggling with keeping my bag on. Any suggestions anyone????
May 7, 2015 at 6:11 pmYour story about your surgery sounds like mine. I had my large intestine removed 8 years ago due ulcerative colitis. Had jpouch for that long. 2 years ago I had surgery for a ileostomy due to crohns. I was in hospital 1 week before my surgery and was put on fluids to build my strength up before the surgery.
August 18, 2015 at 1:25 pmI remember stoma nurse meeting after the surgery to show me how to clean around the stoma and explain how to change the bag. I was in so much pain I was pushing the pain medication button evey 20 min. I was in hospital 28 days.