CSN Login
Members Online: 9

Stomas after Pelvic Exenteration what are they like?

oncebitten2shy
Posts: 5
Joined: Aug 2010

Looking to talk to someone who has had this proceedure done and can tell me about the stomas and the bags. Just want to know what I can expect. Will be having this done in about 3 weeks.

dorsco
Posts: 2
Joined: Jun 2010

I just posted a message on your other post. There are a few ladies on www.inspire.com that have been through this same surgery. There is also some people on UOAA, must do not have cancer diagnosis but they have colostomies and urostomies. I am very sorry that this is happening, I'm not sure why there are a few of us who must go through this but there must be some kind of reason. Please get at least a couple opinions before you go through this. It deffinately sounds like you need exenteration for maybe they don't need both ends and the bladder could be made internally so you don't have 2 bags. Please keep me posted.

Dorie

naggymaggie
Posts: 15
Joined: Nov 2009

I have looked up stoma care because I know it will be the next step for me if the cancer comes back. YouTube videos on urostomy and colostomy ileostomy care seem geared to nurses or caregivers but it is good to see the right way to care for yourself. I am sure that a good quality of life is very much related to quick wound and stoma healing. I hope this helps-I feel for you and wish you the very best!

Subscribe with RSS
About Cancer Society

The content on this site is for informational purposes only. It is not a substitute for professional medical advice. Do not use this information to diagnose or treat a health problem or disease without consulting with a qualified healthcare provider. Please consult your healthcare provider with any questions or concerns you may have regarding your condition. Use of this online service is subject to the disclaimer and the terms and conditions.

Copyright 2000-2014 © Cancer Survivors Network