Having a colostomy for anal cancer
Find out about having a colostomy for anal cancer.
Having a colostomy for anal cancer
Your surgeon forms a colostomy during an operation called an abdominoperineal resection. They remove your anus, rectum and part of your bowel (colon). They then create an opening in the skin of your tummy and stitch the end of your bowel to the opening. The opening is called a stoma.
You put a special bag over the stoma (colostomy bag) to collect your poo (stools). The bag is called a colostomy bag.
Looking after your stoma
After your operation the stoma is swollen, but it gets smaller over a few days. A stoma has no nerves, so it doesn't hurt. It oozes a white mucus, which collects in the bag with your poo.
Learning to look after your stoma takes time. Your stoma nurse will teach you how to care for it. They give you advice on things like travelling or doing sports with a colostomy. You might also have questions about more private things like your sex life. These questions might be hard to ask. But your stoma nurse knows how a colostomy may affect your life in many personal ways. They can give you tips and support.
You can ask the stoma nurse to show a relative how to look after the stoma. This way they can help out when you get home. You can also phone your stoma nurse for advice and support after you leave hospital.
You can view and print the quick guides for all the pages in the treating anal cancer section.
Your surgeon will create a colostomy if you have an operation called an abdominoperineal resection. They remove your anus, rectum and part of your bowel (colon). Then the surgeon makes an opening in the skin of your tummy and stitches the end of your bowel to the opening. The opening is called a stoma.
After your operation the stoma is swollen but it gets smaller over a few days as it heals. It is round or oval in shape, and red like the inside of your mouth. It has no nerve supply, so doesn't hurt. But you have to take care not to injure it because you won't be able to feel pain there.
You put a special bag over the stoma (colostomy bag). Your poo (stools) pass out of the stoma into the bag. As well as passing stools, the stoma oozes mucus. This is normal and it collects in the bag with the poo.
Learning to look after a colostomy takes time. The medical team will help you to cope. There are specialists to help, especially the stoma nurse. They will visit you on the ward before and after your operation and help you to learn to look after your stoma.
The stoma nurse can answer your questions and show you the type of colostomy bag you will use at first. You learn how the bag works and how to fit and empty it. The stoma nurse or ward nurse look after your colostomy and change your bag for the first few days. They gradually encourage you to do it yourself.
The stoma nurse also gives you information about your diet. They can answer any questions you have about practical things, such as
- doing sports
- what to wear
You might also have questions on more private matters like how the stoma will affect your sex life. People often feel too embarrassed to discuss these details. But these questions are natural. Remember that the stoma nurse has experience in this and understands that a colostomy might affect your life in many personal ways. They will give you tips and support.
It is helpful to keep everything you need to change your colostomy together in a bag or in one place. That way, changing the colostomy can happen easily.
Talk to your stoma nurse or the ward nurses about the kind of support you feel you will need at home. You can ask the stoma nurse to show a close relative how to look after the colostomy. This way they can help out when you get home.
Your stoma nurse will give you their contact details before you leave the hospital. You can ring them for advice and support. The nurse may also arrange to visit you at home. Or a district nurse might visit for a few days to make sure you are coping.
Stoma supplies and prescription charges
Your stoma nurse will give you colostomy bags to take home. You will need to get more from the chemist or direct from a local stockist. The stoma nurse will give you the order code for the supplies you need. Make sure you always have plenty of extra supplies so that you don't run out.
The stoma supplies are free but your GP needs to give you a signed prescription. You can also apply for a Medical Exemption Certificate (MedEx) so that all your medicine prescriptions are free. You get the form to apply for the Medical Exemption Certificate from the hospital or your GP surgery.
The Colostomy Association has lists of stockists of colostomy equipment. They also give support and information to anyone with a colostomy.
Adjusting to living with a stoma is not always easy and might take time.
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