What are the lifestyle changes with permanent G-Tube?

Posted by lummy @lummy, Mar 13 4:25pm

Due to the beginnings of possible silent aspiration events and possible aspiration events during eating, what are lifestyle changes like if I were to need a permanent G-Tube. What are the pluses and minuses? What is life like with a G-Tube?
I have not had aspiration pneumonia at this point and am eating regular meals. I eat things that are easy to eat. Also, what are your suggestions for preventing the need to go the G-Tube route? What has worked and what hasn’t worked to prevent going down this route?
I appreciate learning from your experiences.
Thank You,
Phil

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Profile picture for omaest @omaest

I'm writing this early Saturday morning while getting my "breakfast" through my G-Tube. I've had the tube since July of 2024 and without it I'd probably be dead. Mainly because trying to find nutritious foods that I could actually swallow without aspirating was extremely difficult. I was starving myself, becoming more frail and my immune system was extremely compromised. My life has changed because there are very few social activities that are not accompanied without food. Needless to say our restaurant bill is next to nothing. I'm lucky that I do like to cook and bake so I make most of my husband's dinners and he helps me with the tube. I am able to keep up with my hobbies of playing and collecting Mah Jongg sets, knitting, quilting, reading and baking. I've had a few problems with the tube but they were fixed. I am on my third tube, they last anywhere between 6 - 8 months and are easily replaced. Travel is confined but that might be my choice not the choice of others with tubes. More restrictions on my life style are because of my immune system rather than the tube. It took me about a year before I realized I'd be better off with the tube. I wish I had done it before I became so weak. My worry then was the G-tube would shorten my life and make it difficult - the actual opposite has happened, it has added time to my life and for the most part ease. Someone else has added about the necessity of cleanliness with the tube - a must. Also, I have purchase Waterproof PD Dialysis Catheter Wound Cover Shields so I can shower or bathe normally. My surgeon said I could go swimming but I'm not going to chance it. I'll have to get more than one opinion. I hope this helps. Good luck on your journey.

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@omaest
Can you share what you use to cover you tube while bathing? I still leak a little from my mik-e tube so need something that covers it completely. I would love to bathe again

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Profile picture for oldjarhead @oldjarhead

@praying4miracle
Most "Tubies" take baths, swim in pools or the ocean with no trouble...but public hot tubs or public pools are generally avoided. There are a number of Facebook Groups for us folks who are tied to a tube. Indeed I have learned more in those Groups than anywhere else...and I have educated many doctors as I've shared things I've learned. I've had my G-tube three years and now have the low profile MiniOne.

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@oldjarhead
Thank for your share. Can you also give me the name of the Facebook group?

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Profile picture for praying4miracle @praying4miracle

@omaest
Can you share what you use to cover you tube while bathing? I still leak a little from my mik-e tube so need something that covers it completely. I would love to bathe again

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@praying4miracle This is what I order from Amazon:
https://www.amazon.com/dp/B0C7MT8VBH

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Profile picture for oldjarhead @oldjarhead

@lummy

I change my own tubes now, after going to the VA and having an LPN do the change which I did for maybe three changes. I also buy my MiniOne buttons direct from AMT because the VA will only furnish the Avanos Mickey and it is a bit larger than the AMT MiniOne. I keep a couple of spares on hand should the balloon burst.

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@oldjarhead
Thank you for this great information. You are a great resource.
I appreciate you.
Thanks,
Phil

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Profile picture for omaest @omaest

I also had to go to the ER for one exchange because the balloon broke and the tube was too small. There is an office of General Surgeons nearby connected to my health care (Unity Point). I go to either the surgeon who inserted my first tube or the one who saw me at ER. Now, after reading what Gary wrote - I am going to see if I can make an official appointment in 6 months rather than wait for something to happen. The digestive care unit has been less than helpful and has only seen me twice in two years once was after I had developed an infection (surgical stuff left in during the insertion started to fester) and the other time just a check up.

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@omaest Thanks for information.

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Thanks everybody for feedback’

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The Oley Foundation is a leading nonprofit providing support, education, and an equipment donation program for people on tube feeding (enteral nutrition).
They may have helpful resources.

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Profile picture for praying4miracle @praying4miracle

Hi Phil,
Sorry to hear about your pending decision and swallowing challenges. I have been on a g-tube since my botched operation over a year ago.
I have silent aspiration when i eat and cannot drink any thing now after radiation without coughing. I hate to say permanent as I am hopeful. I still eat some to keep the muscles at their best. And am very careful about a clean mouth before eating so if I aspirate it does not turn into pneumonia. Get a tongue scrapper to make sure.
Life with a peg removes the stress around trying to get enough calories in and reduces risk of pneumonia since you are eating. It is tough to watch others eat and not participate. .. times like Thanksgiving and Christmas can be depressing. Maybe some type of combination would work for you.
Peg tube cleanliness is important as they tend to leak a little. This isn't too bad but should be watched to avoid infection. My first one had the tube extender attached and got pulled on clothing when I jogged and after a restless night in bed. There will also probably be extra tissues that grows around the peg as your body tries to heal the incision around the peg which can bleed. I exchanged my original one for a miki (spelling). These need to be changed out periodically...no big deal. 2 minutes process. I have heard that tubes may cause damage to the stomach lining but low risk and I had no choice. Be sure to ask you doctor. Major downside...no submerging in water...no baths or swimming due to risk of infection. Showering is ok.
Hope this helps,
Donna

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@praying4miracle
Donna - what does your tube look like? I'm ready to get another one because of leakage around the tube - I've had this done three times and each time the tube extender was wider around. Each time the extension is also less flexible and my clothing seems to bother it as well as movement of my arms, twisting, etc. I have a G-tube (inserted surgically rather than endoscopically). My issues started when the incision started festering and it was found the surgeon had left a drainage tube or something in my stomach.

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Profile picture for omaest @omaest

@praying4miracle
Donna - what does your tube look like? I'm ready to get another one because of leakage around the tube - I've had this done three times and each time the tube extender was wider around. Each time the extension is also less flexible and my clothing seems to bother it as well as movement of my arms, twisting, etc. I have a G-tube (inserted surgically rather than endoscopically). My issues started when the incision started festering and it was found the surgeon had left a drainage tube or something in my stomach.

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@omaest
See below. Hope this works for you.
Since you can remove the tubes after feeding, it really cuts down on the friction issue. You will need to replace them periodically but it takes two minutes - they use the same hole - just remove the old and replace with a new one.
The nurse assistant was done with mine before I even new it.
Good luck
-Donna

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