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Urostomy takedown

Posted by uroman, on Fri Aug 20, 2010 7:31 am
Looking for anyone who has had a urostomy take down.  Just want info on what to expect.  The reason for my take down to continent urostomy is simpley to get rid of the bag.  I have had no other issues for the past 27 years.

thanks for any information,
Reply by Patches, on Sun Aug 22, 2010 6:27 pm
Do you mean a reversal?
Reply by uroman, on Mon Aug 23, 2010 7:02 am
Yes, well going from incontinent to continent urostomy.
Reply by Miss Scarlet, on Mon Aug 23, 2010 4:02 pm
Hi Uroman
I do not understand what you maen. I have a urostomy and I thought all urostomies were permanent. So if you have the bag taken away what do you get in its place ?
Reply by uroman, on Tue Aug 24, 2010 10:26 am

They'll take a piece of colon and make an artifical bladder out of the colon.  The ureters attach to the new bladder.  There will be a small stoma that will be cathaterized every 4-7 hrs to empty the bladder.  Usually the stoma can not be seen because it is in the belly button.  So with all that said there will be no need to wear an external  pieces to collect the urine.
Reply by Miss Scarlet, on Tue Aug 24, 2010 3:27 pm
Wow Uroman. That sounds amazing. When is your operation. ? Hope it goes well.
Reply by uroman, on Wed Aug 25, 2010 8:56 am
It is scheduled for the 21st of september.  I'm excited but nervous.  I have been so use to what I have for well over half my life.  Thanks for the wishes.

FYI - if you have any interest in making the switch talk to a pediatric urologist.  They have more experience compaired to the adult urologist.
Reply by Catesmom, on Wed Aug 25, 2010 11:28 pm
Wow, I also have a urostomy and never knew that was an option.
Good luck with your surgery.
Reply by uroman, on Thu Aug 26, 2010 8:59 am

Boston Childrens Hospital.  Dr. Nguyen is a pediatric urologist who does this surgery.  In case your interested.

Reply by girlygirl, on Thu Jan 26, 2012 5:21 pm
wishing you every success with your op. wish it was an option for us all but for a lot of us its permanent, but i suppose we learn to live with it..eventually!
Reply by vanessavy, on Mon Sep 03, 2012 8:53 pm
I never knew anyone that had this but I know of people so congrats! It is similar to my contient ileostomy but for the bladder. I debated having one since I have bad Interstitial Cystitis but I am not sure I could manage draining 2 pouches even though I know of a model that has a Kpouch and a Bladder pouch aka The Indiana Pouch.
Reply by Cornet, on Wed Mar 25, 2015 5:40 am

Fascinating topic uroman.  Had heard of this but assumed the bladder emptying was difficult.  I guess by now you've had the op, so would like to hear how its all working.

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