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After any bowel operation, you may notice that certain foods upset the normal working of your bowel (or your stoma, if you have one).
High-fibre foods, such as fruit and vegetables, may make your stools loose and make you pass them more often than normal.
Depending on the type of surgery you’ve had, you may have diarrhoea|. Tell your doctor or nurse if this happens, as they can give you medicine to help. It’s important to drink plenty of fluids if you have diarrhoea.
This is often only a temporary reaction, and after a while you may find that the same foods don’t have any effect. There are no set rules about the types of food to avoid and each person needs to experiment for themselves. Some foods that disagree with one person may be fine for another.
You may also find that your bowel produces more wind| than before, and this can sometimes build up in the abdomen and cause pain. Drinking peppermint water or taking charcoal tablets can help to reduce this. Your doctor can prescribe these for you, or you can get them from your chemist.
It can sometimes take months for your bowel movements to get back to normal after surgery, and you’ll probably need to find out which foods are right for you through trial and error. Some people may find that their bowel is always more active than before their surgery, and that they have to eat carefully to control their bowel movements.
If you continue to have problems, it’s important to talk to a dietitian at the hospital, as they can give you specialist advice for your individual situation.
You may our information on eating problems and cancer| helpful.
Some people with cancer of the rectum will need to have a colostomy. This can be daunting at first. Learning to look after a stoma takes time and patience, and no one expects you to be able to cope straight away. Like anything new it will get easier with time and practice.
In most hospitals there are specially-trained nurses called stoma care nurses (or colorectal nurses) who you’ll usually meet before your operation. They will show you how to look after your stoma and help you cope with any problems.
You may also find it helpful to talk to someone who has already learned to live with a stoma. Your nurse or doctor can often arrange for a volunteer to visit you and talk to you about the more practical and personal aspects of living with a stoma. This advice can be invaluable, particularly in the first few months after your operation. You can also contact the Colostomy Association|.
The Healthtalkonline| website has information about colostomies. It also has video and audio clips of people who have stomas talking about their experiences.
Before your operation, the nurse or doctor will carefully plan the position of your stoma so that your bag stays in place, whether you are sitting, standing or moving around.
For the first few days after your operation, the nurse will show you how to look after your colostomy and make sure that the bag is emptied and changed as often as necessary. At first your stoma will be slightly swollen and it can take several weeks before it settles down to its normal size.
As soon as you’re feeling well enough, the nurse will show you how to clean your stoma and change the bags. There are several different types of bag or appliance available, and the nurse will help you choose a suitable one.
When the nurse is showing you how to look after your stoma, it may help for a partner or close relative to be with you, in case you have any difficulties when you get home.
Before you leave hospital, your nurse will make sure that you have a good supply of stoma bags. Before you start to change or empty your bag, make sure that you have plenty of bags and cleaning materials to hand. It’s a good idea to keep everything you need in one place, so that you don’t have to search for things at the last minute. Make sure you allow yourself plenty of time and privacy, so that you can work at your own pace without any interruptions.
Some people with a colostomy avoid wearing a bag by flushing-out (or irrigating) their colostomy about once a day, although this method doesn’t suit everyone. Your stoma nurse will be able to discuss this with you in more detail.
There are different ways of getting stoma supplies when you’re at home. You can get all your supplies from your chemist. Sometimes it’s better to get your supplies direct from a specialised supply company. These may also offer a cut-to-fit and home delivery service. The Colostomy Association has details of companies.
The supplies are free, but you’ll need a prescription from your GP. If you’re aged between 16 and 60, make sure that your doctor signs the form saying that you’re entitled to free prescriptions.
Once you’re at home you can phone the stoma nurse if you have any problems. Your GP may also arrange for a district nurse to visit you for a few days when you first leave hospital. They can make sure you’re coping at home, and sort out any problems that you may have with your stoma.
Having a colostomy is a big change in your life. Many people find that they are embarrassed by the stoma, and that it affects the way they feel about their bodies. Embarrassment about a stoma can also affect relationships, and some people are uncomfortable about their partner seeing it.
These feelings are a natural part of coming to terms with the changes that a stoma causes, and usually decrease gradually over time.
You can contact our cancer support specialists| if you want to talk about any concerns you have.
Content last reviewed: 1 July 2012
Next planned review: 2014
For answers, support or just a chat, call the Macmillan Support Line free (Monday to Friday, 9am-8pm)
If you have any questions about cancer, need support or just want someone to talk to, ask Macmillan.
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© Macmillan Cancer Support 2013
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