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11 Myths v. Facts About Your Ostomy



After an Ostomy surgery, seeking tips from fellow ostomates in online communication, support groups, and forums can be helpful. Distinguishing between fact and fiction can be tough. With over 112 years of experience among all of our Customer Service Representatives, we have gathered a list of Ostomy Myths vs Facts to provide accurate information about life with an Ostomy.


#1. You must only use the Ostomy Pouching System provided by the hospital or doctor’s office.

Fact: After Ostomy surgery, your stoma and body may undergo many changes. During the initial weeks and months, you may need to adjust your Ostomy Pouching System accordingly.

 

#2. All Ostomy Products are identical, and the type of pouching system you wear doesn’t make a difference.

Fact: There is a wide variety of Ostomy Products available, tailored to meet the unique needs of each individual living with an Ostomy.

 

#3. Your stoma shouldn’t change size a few months after surgery.

Fact: in the weeks and months following Ostomy surgery, your stoma may indeed change in size and appearance.

 

#4. Experiencing skin irritation is just a part of life with an Ostomy.

Fact: Skin damage around your stoma can cause pain and infection. Preventing this damage is crucial for maintaining healthy peristomal skin and your comfort.

 

#5. Having an Ostomy means your significant other won’t love you the same way.

Fact: It is normal to feel anxious about relationships after Ostomy surgery. Open communication with your partner about any concerns is key. Remember, having an Ostomy is nothing to be ashamed of.

 

#6. Odor is inevitable when you have an Ostomy.

Fact: With time, you’ll become more comfortable with your Ostomy Pouch and gain confidence in its ability to control odors.

 

 

#7. Since I have an Ostomy, I can’t enjoy the food I love anymore.

Fact: Immediately after surgery, you may be more sensitive to foods, but this sensitivity can improve over time. Gradually re-introduce different foods into your diet and monitor how your body reacts.

 

#8. Having a Colostomy or Ileostomy means I shouldn’t pass anything from my rectum.

Fact: Even after Ostomy surgery, the colon or rectum may still produce mucus. If have concerns about your output, it’s important to reach out to your healthcare professionals.

 

#9. I can’t get my pouch or wafer wet, so I can’t enjoy water activities or bathe with my pouching system in place.

Fact: You can shower, swim, or even use a hot tub with your pouching system on. If your pouch has a filter, cover it with the provided covers.

 

#10. Having an Ostomy means you can’t wear stylish, form-fitting clothing, and people will notice it.

Fact: Before your Ostomy Surgery, did you notice Ostomy Pouches on others in public? Probably not. Consider using wraps or special undergarments to conceal your pouch and boost your confidence.

 

#11. Insurance doesn’t cover Ostomy care, so I have to pay for my supplies out of pocket.

Fact: Contact your insurance provider to understand what your plan covers and how it pays for Ostomy Supplies.

 

How Can We help?


Whether you’re looking for information on Ostomy care products, troubleshooting common issues, or simply seeking advice on managing day-to-day life with an Ostomy, we’ve got you covered. Our team has the expertise and firsthand understanding to address all your concerns and provide you with practical solutions tailored to your individual needs.



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