Living with a stoma

Here you find information about life with a stoma, how to keep your skin around the stoma healthy, as well as useful online tools for ensuring you still have the right product to troubleshooting any problems you might be having.

Experienced in living with a stoma

Keeping the skin around your stoma healthy

Keeping the skin around your stoma healthy

Taking care of your stoma and the skin around it will ensure that your stoma pouch can work optimally. This will help you feel secure and confident in any situation. How to keep your skin and stoma healthy
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Keeping the skin around your stoma healthy

Most people living with a stoma experience irritated skin now and again. However, irritated skin is not a ‘normal’ skin condition. For your stoma pouch to be comfortable and worry-free, it’s important to prevent skin irritation and maintain healthy skin in the area.

 

The cycle of irritation

Leakage leads to contact between output from the stoma and the skin, which causes irritation. The problem is that once your skin becomes irritated, the adhesive on your pouch won’t attach properly, leading to more leaking of output. A vicious cycle of leakage and skin irritation can develop.


Six steps to healthy skin around your stoma:

  1. Make sure your skin is clean and completely dry before applying the adhesive part of the pouch
  2. Adjust the hole in the adhesive so that it fits exactly the diameter of your stoma. After surgery it’s normal that you body shape will change. It’s important that you keep checking to see if your template is the right size and shape for your stoma. Check this by positioning your cutting template over your stoma to see if the hole fits perfectly.
  3. Regularly check the size of the stoma, especially if you have a hernia
  4. Ensure full contact between the adhesive and your skin by exerting light pressure with your hand
  5. Change your appliance as soon as you feel any itching or discomfort
  6. Make sure to use the stoma appliance and accessories most appropriate for your body profile

Choose the right type of stoma appliance that fits your body

Find the right accessories

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Getting the best fit for your body

Getting the best fit for your body

Every body is different, and your body changes over time. A stoma operation is a big change, so read more about how to get the right stoma appliance to fit your body now. Finding the right product
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Getting the best fit for your body

In the months and years following your operation, you may notice certain changes to your body. These changes can include: 

  • Weight gain or loss as you recover from the illness that caused the operation
  • Fold or scarring of the skin around your stoma
  • Hernia development connected to your stoma

As these changes occur, it’s important that you make sure your stoma pouch continues to provide the right fit.

A tight seal between the pouch and your skin is essential to good stoma care. If, for example, the area around your stoma changes from being regular to being more inwards, it may be time to switch to a convex pouch. You may also need to use additional accessories.

Our online self-assessment tool, BodyCheck, will help you figure out your current body profile and whether your body has changed significantly. It has suggestions for the right pouches and accessories for you.

The Brava online interactive accessory guide can help you to troubleshoot and solve typical stoma pouch issues including skin problems.

It’s a good idea to consult with your stoma care nurse about pouch fit and accessories.

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Coping with pouch issues, ballooning and pancaking

Coping with pouch issues, ballooning and pancaking

Ballooning and pancaking are tricky issues that can occur when using a stoma pouch. But there are things you can do to prevent them from happening. Read more here about these issues and how to deal with them. Read more
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Coping with pouch issues, ballooning and pancaking

Ballooning happens when there’s a build-up of gas in the stoma pouch, making it inflate like a balloon. Pouches have charcoal filters that help deal with wind by deodorizing and releasing it from the pouch. But if the filter capacity cannot handle the gas produced, or if it has become moist or blocked by solid output from the stoma, gas build-up can occur.

What can you do to prevent ballooning?
One of the main ways to prevent ballooning is to minimise the amount of gas your digestive system produces. Chewing food thoroughly really helps, as can avoiding food and drinks that you know make you produce a lot of gas. These could be nuts, beans, fizzy drinks or sparkling wine.

If ballooning does occur, you can release the gas from the pouch in the privacy of a toilet, if you use an open bag or use a two-piece system. Changing the pouch when needed can also help prevent ballooning. Finally, it may be worth trying another type of stoma pouch and filter type.

Pancaking happens when there is a vacuum in the stoma bag and the bag sticks together. This stops the output from dropping to the bottom of the bag and can block the filter. There is then a risk that the pouch will be pushed off the abdomen.

What can you do to prevent pancaking?
Blowing air into the pouch before putting it on will help stop a vacuum from occurring. In addition, a drop of oil or lubricant in the pouch will help the output to get to the bottom of the bag.

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Skin irritation around my stoma

Skin irritation around my stoma

Skin irritation around your stoma is usually caused by leakage of output getting underneath the adhesive of your stoma pouch. It is uncomfortable and can stop your pouch from working well. Read more about what to do if this happens. The skin around your stoma
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Skin irritation around my stoma

The skin around your stoma should look similar to the skin on the rest of your body. Immediately after you take off the adhesive, it may be a little pink, but if this doesn’t fade or if the skin is broken or damaged, your skin may be irritated.

What should I do? 

  • Remove the adhesive and check the back. Is there any sign of faeces or urine that could have caused the irritation?
  • Is there any irritation or damage around your stoma that corresponds to what you see on the adhesive?
  • How well does your pouch fit around your stoma? Is your skin exposed to the output from the stoma due to poor fitting? Assess the diameter and shape of your stoma to see if your template has the right size and shape. Use the release liner from the pouch as a guide and if needed, adjust the hole in the adhesive so that it exactly fits the diameter and shape.
  • What is the position of the stoma opening in relation to the surface of your skin? Is it above the skin surface, level with the skin surface or below the skin surface? If the stoma is level with or below the skin surface, or if it is situated in a deep fold, you may need a different type of pouch or accessories for your body profile. Try the Coloplast BodyCheck tool to check fit.
  • Has the adhesive eroded? If so, the pouch may have needed to be changed earlier. Try more frequent changes or consider an erosion-resistant adhesive if you’re not already using one.

If your skin irritation is caused by other reasons, consult your stoma care nurse or doctor.

Choose the right type of stoma appliance that fits your body.

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Becoming confident with your ostomy!

Who to tell and what to say about your ostomy

Who to tell and what to say about your ostomy

After your surgery, one of the big questions may be: how and who do I tell about my ostomy? Read more
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Who and what to tell about your stoma

Whatever you decide to do, the most important thing is that you are comfortable with your decision. You may want to explain that you had major surgery because of a serious illness and now wear an ostomy pouch. This often leaves few other questions to be asked and people will see that you have a straightforward attitude towards your condition..

Family and friends:

Being open and honest with the people close to you can help you get back to the life you had before your stoma surgery. In the beginning, it’s important for the people closest to you to understand that although you are back home, recovery from major surgery will take time.

Children:

If you have young children or grandchildren you may feel that they are too young to understand. However, children tend to cope well if they are given the information in a simple way. Children will often pick up on secrets and hiding the truth from them can sometimes make them think a situation is more serious than it really is.

At work:

Many people are concerned about telling work colleagues. And just like with family and friends, who you tell and what you tell them is entirely up to you. However it’s usually advisable to ensure that at least one person knows you have an ostomy. Then, in case there are any problems or issues, you will have someone to talk to.

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Holidays and travelling with an ostomy

Holidays and travelling with an ostomy

Having an ostomy needn't stop you from travelling or start planning a holiday a few months after your surgery. Read more
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Holidays and travelling with an ostomy

Travelling:

Having an ostomy shouldn't stop you from traveling. You may, however, need a bit of time to adjust to having an ostomy and feel ready to travel. Start by taking short trips, and see how it goes from there.

Whether you are traveling by car, ferry, train or plane, it’s important to be well prepared. Pack a small, travel changing bag and keep plenty of extra pouches and any other supplies you may need with you.

Flying:

If you are flying, make sure you pack plenty of supplies to take with you on the flight and for while you’re away, plus extra for contingencies. Divide up your supplies in different bags just in case your luggage is misplaced or your flight is delayed. Don’t forget that scissors aren’t permitted in carry-on luggage, so cut all of your barriers to fit your stoma before you fly.

Don’t be concerned about your pouch expanding due to the change in cabin pressure. Ostomy pouches have been designed and tested to withstand pressure changes.

Traveling abroad:

Before you travel abroad, check your travel insurance policy to see how your condition and circumstances are covered while away.

In warmer climates, you may perspire more and thus need to change your pouch more frequently. Always make sure your skin is completely dry before applying a new pouch to ensure a good secure fit. If necessary, use a hairdryer to dry the area – but be careful not to have the heat setting too hot.

You may also be at increased risk of diarrhea or dehydration. Drink plenty of water, and consider bringing medicine to treat diarrhea, just in case.

Once you are on vacation, remember that you can still do all of the same activities you did before, and relax and enjoy yourself.

Vacation tips:

  • Store stoma pouches in a cool place
  • Use bottled drinking water to change your pouch when out and about
  • Apply suntan lotion after you’ve put your pouch on, as the creams may affect the adhesive
  • Seal and empty used pouches and dispose of them with normal trash
  • If you feel a bit self-conscious about leaving pouches in your hotel room, use public trash cans
  • Before leaving for your vacation, find out where you can get professional healthcare assistance at your destination, just in case.
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Going back to work

Going back to work

After surgery, it’s natural to want to get back to your everyday life as soon as you can. Going back to work may be part of that and, with a bit of planning, there’s no reason why it shouldn’t be possible. Read more
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Going back to work

Thinking ahead:

After surgery, it’s entirely possible for most people to go back to work. But when and how you do this really depends on how you feel, the type of work you do, and the stoma operation you had.

Talk to your employer and discuss your options as soon as possible. It may be possible to return to work part-time; this could be particularly helpful when you first go back as you may still feel tired and need time to get used to new routines.

Try it out:

A few weeks before you go back, do a few trial runs where you dress and plan your day as if you were going to work. Think about your diet and when and how many times a day you may need to change or empty your pouch. This will help you to establish routines and plan your day accordingly. Most importantly, it will make you feel prepared.

Tips:

  • Speak to your employer as soon as you can
  • If possible, build up your working hours gradually
  • Check the available changing facilities at work
  • Pack a small changing bag that you can take discreetly to the bathroom
  • Do trial runs before you start work, thinking about diet and clothing etc.
  • If your company provides healthcare insurance, check whether your condition affects the policy
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Dining Out

Dining Out

It's one thing to prepare meals at home. But what if you eat in the restaurant or have something delivered? Here you will find tips on how to prepare properly and what you need to consider. Read more
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Dining Out

Eat carefree - that's how it works

Perhaps this seems like a giant step to you. But there is no reason why you shouldn't eat in a restaurant.

Good preparation is important

You can always contact the restaurant to prepare before you go. And many restaurants put their menu online, so you can always find out what's available before you visit the restaurant.

Where to go

Maybe first choose a restaurant that you already know well. You don't have to be overly cautious, but you should be practical. Order what you feel like, but consider how you react to certain foods. Do not hesitate to ask the waitress which ingredients are used.

If possible, you can also order dishes that you have already tried at home. This will let you know how you are likely to respond. In turn, if you eat more and more different foods gradually, your concerns about eating out will decrease. Even if it is part of your life to drink alcohol at home, it is better to take it slowly. So a small beer is better than a big one. In this way, your body can get used to alcohol more easily and possible reactions can be reduced or even avoided altogether.

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Socializing

Socializing

It's important to socialize. Don't let ostomy hold you back in your social life – enjoy life with friends and family. Read more
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Socializing

Don't let ostomy surgery keep you home

Though most things are easier in the comfort of home, it is really important to get back to living and enjoying all the things that you were doing before your surgery. That includes going out and socializing with friends and family.

Will it be awkward?

It is only natural to be concerned about having to explain your situation to people you don't know. But when meeting new people, remember that you do not owe them an explanation of your condition, and it is totally up to you if and when you choose to tell them.

Have a short explanation ready

Sometimes, preparing a short and confident explanation will help put your mind at ease even if you don't ever use it. For instance, you could simply explain briefly that you went through a serious illness, and because of that you had major surgery and now wear an ostomy pouch.

Avoid being too technical, and try to be open to questions - without over-sharing. Don't feel you have to explain details of your surgery even if they ask.

What about family and friends?

If you are open and honest with the people close to you, it can help you get back to the life you had before your ostomy surgery. It is completely normal if you still feel uncomfortable talking about it right after surgery. Keep in mind that opening up and sharing can be helpful to you and to them.

How to involve your partner

If you have a partner, it is good to have an open and honest discussion socializing with friends and acquaintances. Involving your partner in how you would like to explain your condition if and when you choose to, will help both of you handle the situation more naturally.

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Intimacy and pregnancy

Intimacy and pregnancy

A stoma can affect your body image, but it does not have to affect the relationship with your partner or any pregnancy. Continue reading for easy, practical advice on living with an ostomy. Read more
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Intimacy and pregnancy

Intimacy and pregnancy with ostomy

After ostomy surgery, it is natural that you are worried about the appearance of the body. It may take time to get used to the physical changes and you may feel less attractive as a result. It can be a challenge but it is important to accept it as part of who you are.

What happens to the intimacy?

Intimacy and a normal love relationship can be resumed after ostomy surgery. How and when depends on the type of surgery you have undergone. Impotence and / or discomfort may occur if the rectum or bladder has been removed (women may also be affected).

It is important to talk to your partner and not feel too self-conscious because of the surgery. It is also important to talk to your ostomy nurse who is used to discussing the concerns you are experiencing and can help you in many ways. There are also several handy tips and tricks to cope with everyday obstacles. For example, you can customize lingerie so that they are worn as a tube around the body and cover the bag, or to use mini bags for intimate situations.

Can I have children?

In short, yes. Having a stoma does not prevent a woman from having a baby throughout her pregnancy and giving birth normally. As the stomach grows, the stoma will simply follow the shape of the abdomen as it changes. In later stages of pregnancy you may need to use a mirror when changing your bag. The delivery takes place in the normal way.

Talk about it

There is nothing safer than someone who really understands what you are experiencing. Through your local patient association you can meet other stoma surgeons and get useful tips, inspiration and personal support.

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Diet and Nutrition

Diet and Nutrition

Read what you should consider in the first two to six weeks after the operation and also after your complete recovery - we name a few tips and tricks! Read more
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Diet and Nutrition

Nutrition tips for ostomy patients

In general, people with a stoma can eat and drink what they want, unless the surgeon or stomatotherapist has given them any other recommendations. But just like before the operation, some dishes are easier to digest after the operation than others. And immediately after the procedure, it can be helpful to pay special attention to the body's signals.

Immediately after the procedure

New research has shown that the faster you eat “right” food after the procedure, the faster your digestive system will get going again. Basically: Talk to your doctor about your meal plan after the ostomy.

In the first 2 to 4 weeks
  • Your body is still in the healing process. Food that is easier to digest aids healing.
  • You may feel a little bloated. So try to eat only a little at a time and eat more often.
  • Easily digestible dishes are a good start.
  • Chewing thoroughly is very important for good digestion.
4 to 6 weeks after the ostomy
  • Sometimes the appetite subsides in the first four to six weeks after the ostomy / surgery.
  • It may therefore be necessary to supplement your diet with proteins *.

Are there dishes that I am not allowed to eat?

There is no reason to avoid certain foods. But it's good to know that different foods affect stool properties in different ways. If you are unsure about a particular food, try a small amount first. If you don't have any problems - enjoy it! We recommend that you keep a food diary where you can record what you have eaten and what the effects are.

Don't be afraid of new dishes - but everything with reason. You may notice that certain foods cause more bloating than others. And even if these foods are not bad for you, you may want to reduce them a little. The same applies to chewing gum.

Just experiment and discard what is not good for you - you will find a balanced diet that suits you. Some foods, especially fiber-rich foods, can lead to regular constipation, in which undigested foods block the intestines. Chewing thoroughly can help, but constipation can be a serious problem. Read more about constipation further down this page.

What about fruits and vegetables?

You can still eat the famous "five servings" every day! The skins of some types of fruit and vegetables are quite firm. Therefore, it is best to peel them to avoid problems. This is especially true for potato and apple skins. And maybe you just have to prepare fruit and vegetables in a new way. with vegetables in the form of soups or fruit as fruit smoothies?

If vegetables get a little softer while cooking, this is also helpful. And root vegetables can be used to make mashed or puree very well.

When an accident occurs?

A bad experience should never result in you giving up a particular food. Only in the case of repeated problems should you perhaps better remove the "wrongdoer" from the menu.

And please remember: everyone reacts individually. What is good for one person does not necessarily have to fit for another.

 

* After consulting your doctor.

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Beverage and Drinks

Beverage and Drinks

As with everyone else, the drinks you consume affect the digestive tract. Here you can find tips for people with ileostomy and colostomy. Read more
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Beverage and Drinks

Drinks affect the digestive tract

If nothing speaks against it, you should consume at least two liters of fluid ** a day. This also prevents constipation. But you may be wondering if you can still enjoy your morning coffee, a glass of wine, or carbonated drinks.

Here are a few pointers:

  • Coffee and tea are fine, but as usual, you should pay close attention to any reactions in your digestive tract.
  • Carbonated drinks can lead to gas formation.
  • Beer can make the stool more fluid.
  • You can drink alcohol. However, alcohol can promote dehydration. So make sure you have enough water.
Especially for people with ileostomy

You can lose fluid especially after the procedure due to the relatively high amount of stool (approx. 1,500 ml). If nothing speaks against it, it is recommended to drink at least two liters of water daily plus the corresponding amount of fluid lost through the stool.

Three to twelve weeks after the procedure, the small intestine gradually gets used to absorbing more fluid and you may not have to compensate for the loss of fluid as you did in the beginning. Patients with ileostomy lose two to three times more fluid and electrolytes through stool than others.

 

** After consulting your doctor and if there is no disease that requires volume reduction.

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Tips for flying

Tips for flying

You may have some concerns if you are travelling by plane – what do you do in the security check? Can the bag explode under air pressure? Or what about noises? Read more
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Tips for flying

Before you go

When booking your ticket: it might be a good idea to book a seat near the toilet as it might help take away some of your concerns and make you feel more confident as well.

You can bring as much as you can in your hand luggage within the requirements of the airline, but since you will not be allowed to bring scissors in your hand luggage we recommend that you cut all your barriers to the right size before you fly.

Going through security

The security scanner might detect your pouch, but you do not have to show your pouch, and security should not ask you to remove clothing to expose it or let them touch it. You may be asked to rub your hand against the pouch on the outside of your clothes, but that should be the extent of the examination. You can always show them your travel certificate, which explains your condition, the medical supplies you are carrying and why you might need support and privacy.

In the air

There is a slight risk that the pressure will cause the pouch to balloon. If this should happen all you need to do is go into the bathroom and take out the air. And remember that just as often ballooning is caused by something you ate or drank – so when you're flying be extra careful with carbonated drinks. If you are a little self-conscious about noise from the pouch, you will be pleasantly surprised by how noisy an airplane cabin is.

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Warm climate

Warm climate

Warm climate and sunscreen can affect the adhesion, but help is here - there are a few things you can do to make the barrier stick better. Read more
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Warm climate

Warm climate

If the climate is warm enough to make you perspire more than usual, the barrier might lose adhesion and you may need to change your pouch more frequently.

Make sure your skin is completely dry before you apply a new barrier for good adhesion. It can be a bit tricky if the weather is very hot and humid – if drying your skin is difficult, you can use a hairdryer on low heat to dry the area (but be careful that it does not get too hot and keep it away from the stoma itself).

Sun lotion

Apply sunscreen after you put on your barrier, as the lotion could affect the baseplate and make it harder to stick. Read about applying sunscreen in the 'use sunscreen' section.

Storage

We recommend that your supplies are stored in a cool place – do not leave your ostomy products e.g. in the car for long periods during hot weather, since the heat may damage the adhesion.

Storage

Talk to your stoma nurse – and get the products you need

Talk to your stoma nurse – and get the products you need

When spending time in a warmer climate you might need a few more products than usually. For some people a skin barrier that helps the adhesive stick better can be very helpful, and if it is the edges not sticking properly an elastic tape can be a possible solution. Some benefit from using a antiperspirant on the skin in the area to be covered by the adhesive. 

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Beach and Swimming

Beach and Swimming

Going swimming can be a big thing when you have an ostomy – what to wear? Will the barrier stick? Read a few tips here. Read more
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Beach and Swimming

What should you wear for beach- and swimwear?

The most important is that you wear something that makes you feel good – feel as you. Some people do not mind showing their bag when going to the beach, whereas some prefer covering up. Do what makes you feel the best. Unfortunately, buying specialty swimwear is no guarantee of a good fit. On the other hand, you might be able to find regular swimwear that fits your need perfectly.

On the beach, a sarong or wrap can be a great way to gracefully cover up without feeling out of place.

Swimming

Always make sure that the barrier sticks properly before going swimming – give it some time after applying. Be aware that the water can affect the adhesion negatively, so make sure to change your product more frequently if needed. For some people it can be helpful to use accessories when going swimming – using a skin barrier that helps the adhesive stick better can be very helpful, and if it’s the edges not sticking properly an elastic tape can be a possible solution.

It is always a good idea to talk to your ostomy nurse if you have any questions. You can also contact one of our customer service representatives at 1800 102 0550.

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How to prevent the stoma from smelling

How to prevent the stoma from smelling

The fear of smell from the ostomy bag is a well-known problem for most people who have an ostomy. However, the reality is that most ostomy bags prevent all odor from coming out. Read more
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How to prevent the stoma from smelling

Odor, or the fear of odor from the ostomy bag, is a well-known problem for most people who have an ostomy. However, the reality is that most ostomy bags are made of material that prevents all odors from coming out, and that most also have a filter that removes odors from intestinal gases. However, if the bag is not changed often enough, the filter can be blocked by feces, which can cause odor.

If you use a disposable bag and you do not clean the outlet properly after emptying, odor can easily escape into the environment. Thoroughly clean the outlet to avoid this.

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Sun Safety

Sun Safety

Staying in the shade is an effective way to reduce sun exposure - especially between 10AM and 4PM when the sun is at the highest point. Read more
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Sun Safety

Did you know that skin can burn in just 15 minutes in the summer sun?

Staying in the shade is an effective way to reduce sun exposure. You can use trees or built shade structures, or bring your own umbrella to the park, beach, etc.!

Whatever you use for shade, make sure it casts a dark shadow. Though being in the shade it is still recommended that you use other protection - such as clothing, hats, sunglasses and sunscreen.

 

These guidelines are not exhaustive and you should always seek advice and guidance from professional if you have any doubts.

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Exercise with Ostomy

Exercise with Ostomy

Many believe that they can no longer exercise or perform physical activities when they have an ostomy. There are many different types of exercise - find one that you like. Read more
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Exercise when having an ostomy

Exercise is healthy and there are few physical limitations to participate in recreational activities after receiving a colostomy or ileostomy.

Once you have recovered from the surgery, you can return to most of the activities you did before, sports, gardening, etc. However, we recommend that you contact your doctor or ostomy therapist before resuming / starting these activities again.

If necessary, the stoma can be protected with a special protective accessory, contact your stoma therapist.

  • Cycling, ball sports, golf and similar sports usually do not cause problems, but you should avoid physical sports such as boxing for practical reasons.
  • Weightlifting should also be avoided as it may increase the risk of developing a sliding hernia.
  • Exercising a more strenuous sport and getting sweaty can affect the durability of the booklet. Therefore, it is a good idea to change the booklet before exercising to ensure that the bandage is held securely in place.

Most often, the biggest challenge when participating in various sports is psychological. Unfortunately, the experience of leaks, or the fear that the bag will leak, causes some people to avoid sports activities.

When you participate in team sports, you rarely have the opportunity to shower individually. Some people with an ostomy may find it very difficult to undress in front of others and thereby show their ostomy. Teammates can notice this which can lead to curious questions, but it should not limit your willingness to participate.

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Upholstery tips

Upholstery tips

Your stoma does not prevent you from wearing certain types of clothing - the most important thing is that you wear something that makes you feel good. Read more
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Upholstery tips

You can probably dress like you did before your surgery. The most important thing is that the clothes do not prevent the stool from falling into the bag.

The stoma must be positioned so that it does not get in the way of the type of clothing you usually use. In most cases, this means that it must be placed below the waist, where it would otherwise be subjected to friction from the waistband / belt. Tight waists over the stoma should be avoided as they can push against the bag and cause leakage or even prevent the stool from leaving the stoma.

For men, it may be more practical to use braces instead of a belt, but some may still prefer to use braces only when they have a blazer or similar at the top.

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Ostomy Care Patient Testimonials

"Clothes are a part of my identity, so I worried about what I could wear after my operation. Today, I still dress the way I want."

"I was so glad to get back to work, it meant a lot to me. At first I worried about my ostomy appliance, but now I'm just focused on the job."

"I lost 35 kilos when I was ill. But I have put it all back on. I feel determined, I'm training regularly and I'm now a specialist personal trainer."

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