← Return to 365 days later after surgery to remove esophageal cancer at Mayo

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@mrgvw

Where are you on your journey?

What stage are you?

Where is your treatment being done?

I have definite thoughts on this... not a fan of stents in general, although I can think of instances where they do have their uses (but very few). If you are in this for the long haul... and you are eligible for the J tube surgery, then this is the way to go. It is simply a tool to help you on your EC journey... they take it out of you in about 30 seconds, in a doctor's office, when it is no longer needed. I had mine for 8 months, 4 before my esophagectomy, and 4 after.

You wanna chat all things J tube, swallowing, stretches, stents, etc... just private message me. Be well...

Gary

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Replies to "Where are you on your journey? What stage are you? Where is your treatment being done?..."

I had a J tube for a few months following Stage 4 Esophageal Cancer surgery. The last few months were spent in nursing facilities which I found to not be very good for patients. Of the 4 places I was in, 95% of the nurses caring for patients didn't know the difference between a "J" tube and a "G" tube. Consequently, they thought nothing of crushing my meds and running them thru my J tube which clogged it up like cement. The G tube is larger & goes into the stomach & the smaller J tube goes into the intestine. Unclogging rarely worked and twice I had to go to ER to have the damaged tube removed and replaced with a new one. One nurse tried pouring hot water from the coffee maker into the tube which then exploded and the extremely hot water seriously burned my abdomen. I was so glad to get the tube removed after I finally returned home after 7 mo. of confinement.