Ostomy: Adapting to life after colostomy, ileostomy or urostomy
It takes time to become comfortable with an ostomy — a surgically created opening in your abdomen that allows waste or urine to leave your body.
Many questions may run through your mind as you practice good ostomy care and live your life. It can help to talk to others who have been there. Perhaps you'd like to ask others questions like: What can I eat? What about leaks? Can I go back to work after colostomy? Can I ride a bike with an ileostomy? Will everyone figure out I've had urostomy surgery just by looking at me? What about intimacy?
Welcome ostomates. Let's talk frankly about living with an ostomy. Why not start by introducing yourself? What type of ostomy do you have? How's it going?
Interested in more discussions like this? Go to the Ostomy Support Group.
Adapt——recommended by ost run’s at Mayo. Made by hollister
I use the bags w/ filters. They help to eliminate some of the gas build up, but then the side effect is that the gas escape at not always the best time. It is really uncontrollable farting.
I don’t believe I could be much help on this one. My husband has a urostomy and we have not had problems with odor with his pouch. We do use Lysol spray around the bedroom due to the night bag. Wish I could be more help.
I m74and have a colostomy 39 years ago never had any issues with it. I was lucky that I didn't have cancer. I farm, drove truck and work in a grain elevator. I've had a normal life with it
Welcome, Mick. 39 years, wow. What has changed over the decades with colostomy pouches/devices? What improvements have been most grateful for?
I use converted wafers and pouches. The biggest change was when they went to predict for the stone Other wise there hasn't been any changes. At first I had to watch what I ate but through the years I can eat most food. All I can say is I am lucky not to have any problems. Thanks for letting me share.
I have gotten several antibiotic resistant UTI's and a few regular UTI's since getting my Urostmies in May 2020. I don't get any of the typical symptoms because I had a cystectomy. I never knew I had one unit it reached my kidneys making me really, really sick ending up hospitalized. I am getting better at noticing even the slightest changes in my urine such as smell, foamy, etc. I use OTC (AZO) urinalysis sticks and/or drop by my Uro's office to drop off a be sample (so they can also run a culture). Getting a clean catch when sporting bilateral urostmies is a challenge as well. Getting a sample from a bag is simply not accurate in my mind. You just need to be very in tune with your body. It has taken me a while but I'm getting better at it.
Hi I'm Catelynn I also had an ileostomy and am seeking support in coping with issues re: same
I am new to Mayo clinic support group
Hi Catelynn, welcome. Tell us a bit more about yourself. What led to your needing an ileostomy? What challenges are you coping with?