Although it can be difficult to adjust at first, having an ileostomy does not mean you cannot have a full and active life.
Many people with a stoma say their quality of life has improved since having an ileostomy because they no longer have to cope with distressing and uncomfortable symptoms.
But if you're finding it difficult to adjust after your operation, it may help to get in contact with others who have had similar experiences through support groups like the Ileostomy and Internal Pouch Support Group.
You may also find the following information useful if you have an ileostomy, or are due to have one in the near future.
Before and after the ileostomy procedure, you'll see a nurse who specialises in helping people with a stoma.
The nurse will advise you about equipment you'll need and how to manage your stoma.
Your stoma will produce liquid digestive waste that can range from a watery consistency to a consistency similar to porridge, which is collected in a stoma bag.
There's a wide range of stoma bags available, but a specialist stoma nurse can help you choose the most suitable appliance for you.
To help reduce skin irritation, stoma bags are made from hypoallergenic (non-allergic) material, and contain special filters to help ensure the bags do not release any unpleasant odours.
They can be easily drained through an opening in the bottom and can be concealed under everyday clothes.
It's usually best to empty your bag into a toilet when it's about one-third full as this prevents the bag bulging underneath your clothes.
You'll usually be advised to replace the bags and dispose of them in the general rubbish (not down the toilet) every 1 or 2 days.
At first, living with an ileostomy can be a distressing experience. It may take some time before you get used to it, but with practise and the support of your stoma nurse and family, using stoma bags will become routine.
There are also additional products that can make living with an ileostomy more convenient.
Your stoma care nurse will be able to advise you about the most appropriate equipment to help you manage your ileostomy successfully.
If you have an ileostomy, you'll be entitled to free NHS prescriptions for necessary products.
You'll be given an initial supply of stoma bags before you leave hospital, as well as your prescription information.
Let your GP know your prescription information so they can make a note of it in your medical records and issue prescriptions in the future.
Your prescription can either be taken to the chemist or sent to a specialist supplier who will deliver the appliances.
There's no need to stockpile supplies, but it's recommended that you order more appliances while you still have plenty left so you do not run out.
The output of your stoma can cause irritation to the skin surrounding the opening, so it's important to keep the skin clean.
You should regularly clean the area using mild soap and water.
You may notice small spots of blood around the stoma when you clean it. This is perfectly normal.
It's caused by delicate blood vessels in the tissues of the stoma, which can bleed easily. The bleeding will soon stop.
Burning or itching skin is a sign that you need to change your equipment.
If a large area of skin becomes inflamed, contact your GP or stoma nurse, who will be able to prescribe a cream, powder or spray to treat this.
In the first few weeks after surgery, you'll usually be advised to follow a low-fibre diet.
This is because having a high-fibre diet can make the consistency of your stools thicker, which can cause the bowel to become temporarily blocked.
After around 8 weeks, you'll usually be able to resume a normal diet.
As you recover, you should try to eat a healthy, balanced diet that includes plenty of fresh fruit and vegetables (at least 5 portions a day) and wholegrains.
If you decide to introduce new foods into your diet after surgery, try to introduce them slowly, at the rate of 1 type of food each meal.
This will allow you to judge the effects of the food on your digestive system.
You may find it useful to keep a food diary so you can keep a record of the food you have eaten and how you feel afterwards.
For example, you may find you experience diarrhoea after eating spicy foods, or after drinking alcohol or caffeinated drinks.
If you no longer have a large intestine (colon), you're at greater risk of dehydration.
This is because one of the functions of the colon is to reabsorb water and minerals back into the body.
It's therefore important to drink plenty of water if you have an ileostomy, particularly in hot weather or during periods where you're more active than normal.
Sachets of fluid replacement solutions for dehydration are also available from pharmacies.
In the first few weeks after surgery, you may experience a lot of gas (flatulence).
This is harmless, but it can be embarrassing and uncomfortable. It should subside as your bowels recover from the effects of surgery.
Chewing food thoroughly and not eating foods that cause gas can help.
Fizzy drinks and beer also cause gas. Do not skip meals to try to prevent gas as it'll make the problem worse.
If the problem persists, your GP or stoma nurse should be able to recommend a medicine that can help to reduce gas.
Many people also worry their external bag will smell. But all modern appliances have air filters with charcoal in them, which neutralises the smell.
If necessary, special liquids and tablets that are placed in the bags are available to reduce any odour.
Many medicines are designed to dissolve slowly in your digestive system.
This means some medications may not be as effective if you have an ileostomy as they could come straight out into your bag.
Let your GP or pharmacist know about your stoma so they can recommend an alternative type of medicine, such as an uncoated pill, powder or liquid.
In women, having an ileostomy can affect the effectiveness of oral contraceptive pills, so you may want to discuss alternative forms of contraception with your GP or pharmacist.
Once you have fully recovered from surgery, there's no reason you cannot return to most of your normal activities, including work, sports, travelling and having sex.
Speak to your stoma nurse before returning to your normal activities, however, as they can offer advice about issues you may need to take into consideration now you have an ileostomy.
For example, they can advise you about wearing protective stoma guards while playing sports, or stocking up on ileostomy products before travelling.
Living with an ileo-anal pouch is different from living with an ileostomy because the procedure does not involve creating a stoma in the tummy (abdomen).
Instead, digestive waste is stored in an internal pouch and excreted through the rectum and anus.
If you have had an ileo-anal pouch, you may find you need to empty it up to 20 times a day during the first few days after the operation.
But the number of times you need to go to the toilet will slowly reduce as the pouch expands and you get used to controlling muscles that surround it.
Most people find their pouch activity settles down after 6 to 12 months, although the number of bowel movements will differ from person to person.
Exercising the muscles that control the passing of stools (pelvic floor muscles) can help make going to the toilet easier if you have an ileo-anal pouch.
It can also reduce the likelihood of accidental leaks during the first few weeks after the operation.
Pelvic floor exercises, as outlined below, are a good way of improving your muscle control:
Ideally aim for 10 short, fast and strong contractions.
Anal soreness or itchiness is common in people with an ileo-anal pouch. Having regular baths should help relieve this.
Using a skin protection cream is also recommended. Your GP will be able to advise you about the best cream for you.