Living with bladder cancer
During surgery to remove your (cystectomy), your surgeon might make an internal pouch to hold urine. This operation is called a continent urinary diversion, or a mitrofanoff.
On your tummy (abdomen) you have a small hole called a . To pass urine, you pass a thin tube ( ) into the stoma. The catheter goes all the way into the internal pouch. This allows you to control (be continent) when urine comes out. You don’t have to wear a bag to collect urine, as you would after a urostomy.
You will need to learn how to look after your stoma and pouch. The nurses will show you how to:
empty urine from your pouch
wash out your pouch
Find out about having surgery to make an internal urine pouch
After your operation, you have a catheter in the new opening on your (stoma). This drains your urine. You have the catheter while your body heals. It is in place for about 6 weeks after your operation.
You go home with the catheter in place. Your nurse will show you how to care for it.
After this time you’ll come back into hospital. Your doctor or nurse will remove the catheter. Your stoma nurse will then teach you how to empty your pouch and wash it out.
You empty urine from the pouch by putting a catheter into the stoma. This is called self catheterisation. Your stoma nurse shows you how to do it.
To start with, you empty the pouch every 2 hours or so. As the pouch gradually stretches, you empty it every 4 to 6 hours during the day.
To empty your pouch you need:
a disposable catheter
lubricating gel
a container to drain urine into, or access to the toilet
gauze / tissues
You may also want a mirror to begin with to be able to guide the catheter into your stoma.
At first, you might drain the urine into a container. This is so that your nurse can keep a record of how much urine you are passing each time. After a while you can drain the urine straight into the toilet.
You don't have to worry about keeping everything free from germs (sterile) when you self catheterise. But try to be as clean as possible. You want to keep the risk of introducing an as low as you can. It’s best not to touch the end of the catheter that you are going to put into the stoma.
To empty your internal pouch you should:
wash your hands
open the catheter packaging
open the gel
take out the catheter and moisten the blunt end with water or gel (unless it is pre lubricated)
look at your stoma to check it is clear of any mucus
use a tissue with warm water to wipe away any mucus
make sure one end of the catheter is in the container or toilet ready to collect urine
gently feed the catheter into your stoma
keep feeding the catheter in until urine starts to come out, then insert it a further 4 to 6 cm
drain the urine into the container or toilet
when no more urine comes out insert the catheter in a little more to make sure no more urine is left inside
gently remove the catheter out of your stoma
throw the catheter away
wash your hands
Sometimes you may have trouble getting the catheter in. If this happens, try pulling it back a bit and gently pushing it in again. It can help to roll the catheter between your fingers as you put it in.
Washing out your pouch is also called irrigating the pouch. Mucus can build up inside the pouch. So you might need to wash this out regularly. If mucus builds up in the pouch, the stoma can stop draining properly. You can develop bladder stones or problems with infection.
Your specialist nurse tells you how often you need to do this. It varies, and the advice is different for each person.
To wash out your pouch you need:
a disposable catheter
lubricating gel
cooled boiled water for irrigating
50ml catheter syringe
container for your the waste, or access to a toilet
Start by emptying the urine out of your pouch with the catheter. But leave the catheter in after the urine has all drained out. Then:
pull up the irrigating solution into the syringe
fit the syringe onto the end of the catheter
gently push the end of the syringe in so that the water is pushed into your pouch
disconnect the catheter and empty the contents into the toilet or gently withdraw the contents (follow the advice given to you by your stoma nurse)
fill the syringe again and repeat
keep irrigating and emptying the syringe until there is no more mucus and the fluid that comes out is clear
gently pull out the catheter and throw it away
Your doctor or stoma nurse might prefer you to use sterile salt water solution (saline) or bottled water. Different people prefer one solution to another, but they are all fine to use. You can use bottled water to wash out the pouch if you’re away from home.
The amount of mucus your pouch produces might decrease with time. So you may be able to irrigate less often. Eating certain foods, colds or hay fever will also cause more mucus to develop. You can eat less of these foods to reduce the amount of mucus you produce.
Stoma appliances are products such as and catheters to help you care for your stoma.
Find a stoma appliance supplier
Some organisations can give you advice and support. They might be able to arrange for you to meet other people with an internal urine pouch.
Meeting someone who has been through a similar experience might help you to cope. They know what is important to tell you. And they can answer your questions from first hand experience.
Last reviewed: 01 Oct 2025
Next review due: 01 Oct 2028
Your surgeon makes an internal pouch to hold your urine, and a new opening (stoma) on your tummy. You pass a thin tube (catheter) into the stoma to pass urine and you don't have to wear a bag.
Coping with bladder cancer can be difficult. There are things you can do and people who can help you to cope.
There are organisations and support groups to help you cope with bladder cancer and its treatment.
Get practical and emotional support to help you cope with a diagnosis of bladder cancer, and life during and after treatment.
Bladder cancer is cancer that starts in the lining of the bladder.

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