Hi Everyone! Somewhat new to forum, though totally searched this site since my UC flared and my GI Dr. recommended (May 2013)I move on with my life and have j-pouch surgery. I totally appreciate the info and discussions here as I take this journey.
Had my step 1 in October 2013, and it was a cakewalk! I felt great 2 weeks out, and was able to manage my ostomy, after trying many different appliances. January 2014 was my 2nd surgery,and all went well. However once I got home I began having blockages- mostly due to motility issues, swelling/ inflammation, and a little piece of intestine flapping and blocking output. After many blockages (8-10), 2 admissions back to hospital through ER, I am home with a TPN (PICC line)for nutrition and IV fluid until I can begin eating again. Did ice chips 8 days after last hospital admission/blockage, moved to clear liquids, and unsuccessfully tried cream of wheat cereal yesterday - another blockage.
Have loop ileostomy this time, am trying to hold off til the 2-3 month mark to do takedown, tho my j-pouch was tested and is viable. Not on any meds. I am getting support from surgical team- just checking in here for thoughts/ ideas from people who have experienced this.
Sooo... My questions to you all with real experience is
1. Has anyone else experienced multiple blockages with the loop ileostomy and if so how long before you could eat? Did the blockages continue after take down?
2. I'm having lots, lots clear liquid out the back end/ anus. They think it's coming from pouch. I am also having some mucous which I know is typical, though I could control it after first surgery. Gravity definitely plays into it, as it happens mostly when
I stand. They also think perhaps the increased liquids from TPN may be contributing. Has anyone else experienced this? Most leakage info I've found on this site and others relates to after take down.
Obviously, my concern is that this lack of control (sphincter muscle?) will continue after next surgery. Any ideas, suggestions, experiences would be greatly appreciated!
Sorry to make this post so long- just didn't want to leave out important info! Thank you!
Had my step 1 in October 2013, and it was a cakewalk! I felt great 2 weeks out, and was able to manage my ostomy, after trying many different appliances. January 2014 was my 2nd surgery,and all went well. However once I got home I began having blockages- mostly due to motility issues, swelling/ inflammation, and a little piece of intestine flapping and blocking output. After many blockages (8-10), 2 admissions back to hospital through ER, I am home with a TPN (PICC line)for nutrition and IV fluid until I can begin eating again. Did ice chips 8 days after last hospital admission/blockage, moved to clear liquids, and unsuccessfully tried cream of wheat cereal yesterday - another blockage.
Have loop ileostomy this time, am trying to hold off til the 2-3 month mark to do takedown, tho my j-pouch was tested and is viable. Not on any meds. I am getting support from surgical team- just checking in here for thoughts/ ideas from people who have experienced this.
Sooo... My questions to you all with real experience is
1. Has anyone else experienced multiple blockages with the loop ileostomy and if so how long before you could eat? Did the blockages continue after take down?
2. I'm having lots, lots clear liquid out the back end/ anus. They think it's coming from pouch. I am also having some mucous which I know is typical, though I could control it after first surgery. Gravity definitely plays into it, as it happens mostly when
I stand. They also think perhaps the increased liquids from TPN may be contributing. Has anyone else experienced this? Most leakage info I've found on this site and others relates to after take down.
Obviously, my concern is that this lack of control (sphincter muscle?) will continue after next surgery. Any ideas, suggestions, experiences would be greatly appreciated!
Sorry to make this post so long- just didn't want to leave out important info! Thank you!