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Feeding Tubes and Dysphagia: What You Should Know

Feeding Tubes and Dysphagia: What You Should Know

People with dysphagia, or difficulty swallowing, sometimes cannot eat or drink enough by mouth to stay healthy and safe. When this happens, doctors may recommend a feeding tube. A feeding tube is a medical device that helps a person get the nutrition, fluids, and medicine they need.

Even though feeding tubes are common, there are still many misunderstandings about them. This article will explain why feeding tubes are used, what types exist, and the truth about some common myths.

Why Would Someone Need a Feeding Tube?

Swallowing disorders can result from neurodegenerative diseases, stroke, brain injury, head and neck cancer, and a number of other conditions. If a person is at risk of choking, aspirating, or is not getting enough nutrition, a feeding tube may help.

A feeding tube can be temporary or long-term, depending on the cause of the swallowing problem and how well the person responds to treatment.

Types of Feeding Tubes

  • NG Tube (Nasogastric Tube)
    A thin tube that goes through the nose, down the throat, and into the stomach.
    Often used for short-term feeding (days to weeks).
    Placed at the bedside without surgery.
  • G-Tube (Gastrostomy Tube)
    A tube placed directly into the stomach through a small opening in the belly.
    Used for longer-term feeding (weeks, months, or longer).
    Requires a minor surgery or endoscopic procedure.
  • J-Tube (Jejunostomy Tube)
    Similar to a G-tube, but goes into the small intestine (jejunum) instead of the stomach.
    Used if the stomach cannot be used for feeding (e.g., slow stomach emptying or high risk of reflux).

Your doctor and care team will choose the best type of feeding tube based on your health and medical needs.

Common Misconceptions About Feeding Tubes

  • Myth 1: “A feeding tube means I’ll never eat by mouth again.”
    Fact: Many people with feeding tubes still eat various amounts or consistencies by mouth, if it’s safe. Others use a feeding tube while they work on swallowing exercises. Some people recover enough to stop using the tube altogether.
  • Myth 2: “Feeding tubes are only for people at the end of life.”
    Fact: Feeding tubes are used at all stages of life and recovery. Children and adults may use them temporarily after illness, surgery, or injury. In fact, multiple studies have shown that feeding tubes do not prolong life or prevent aspiration in patients with advanced dementia.
  • Myth 3: “Having a feeding tube means I failed.”
    Fact: A feeding tube is a medical tool—not a sign of failure. It gives your body what it needs so you can stay strong, healthy, and focus on recovery.
  • Myth 4: “Feeding tube food isn’t real food.”
    Fact: Tube feeding formulas are made to meet a person’s nutrition needs. Some people even use blended real food through their feeding tube. Dietitians can help you choose the best option.

Conclusion

Feeding tubes can feel overwhelming at first. But for many people with dysphagia, they are an important part of treatment and healing. A feeding tube may help prevent malnutrition, dehydration, and reduce the risk of aspiration pneumonia, and allow people to focus on getting better.

If you or someone you care for is considering a feeding tube, talk to your doctor or a speech-language pathologist (SLP) who specializes in swallowing. Ask questions and learn about your options. Join our virtual or Facebook support groups to connect with others to learn about their experiences.

Additional Resource:

The Oley Foundation: www.oley.org

 

 



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“Traveling Space Available” (III)



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Report from Old Greenwich



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“Traveling Space Available” II

Mackenbach, Germany

December 3, 2016 at 0900 hours

Many years ago, I wrote an article for a travel magazine called “You and Europe” in a city not far from here. The article, which dealt with hitchhiking rides on military aircraft throughout what we used to call the “European Theater” was titled “Traveling Space Available.”

Now, years later, and traveling with a gastric tube feeding apparatus on board and a supply of formula, I find those words take on a very different meaning. Will there be space available on the airplane for my supply of formula? Is there “space available” in the cabin for the occasional and necessary feedings? Can I replenish my supply of formula while traveling here in the USA and abroad? Will I join my wife or others for meals out in cafes or restaurants? Is it all worthwhile? continue reading →



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My Belly Has Two Buttons

meikeleBy Meikele Lee, author of the children’s book “My Belly has Two Buttons” and lives in Helena, Mt.  She received a 2017 Purple Dragonfly Book Award; Honorable Mention in the category Special Needs/Disability Awareness. She is a wife and mother to 3 amazing children, one of whom has a feeding tube.  She has been in cosmetology for over 10 years, but became passionate about blogging when her youngest child’s oral aversions became life threatening.  She used blogging to try and understand her son’s condition and how he can relate to others with or without a feeding tube, and to help educate the public about these life saving devices. continue reading →