Cancer Support and Caregivers Who Are Trail Blazers!

[clay]

Originally Posted by Wrang1er

I agree wholeheartedly about the nurses!

They are taking that PEG tube out tomorrow. I think you are right, Clay, regarding the stoma. You can see that it's much wider than the tube. I believe from all the pressure put on it from vomiting.

She now has an NGtube which is sucking all that nastiness out of her. She's experiencing pain but she's getting Dilaudid through her IV every four hours. She's also getting fluids. No food or drink though.

I had to laugh earlier. She asked the nurse for ice. The nurse complied but with instructions that she can only have a little.

I left the room and when I came back she was still eating ice. I told her she's only allowed a few pieces. She replied that she knew but she was addicted to it. She's a little out of it.

Hey Wrang! Good on getting j-peg out. I have to tell you, I had an NG tube for 5 weeks back in December when I got so sick & was in hospital for 50 days, had surgery, too. They put a PICC line in my arm, into my superior vena cava to give me TPN (total parenteral nutrition)...a specially mixed bag of lipids(fats), nutrients, vitamins, minerals, electrolytes, etc, that I had for 2 weeks.

As far as her eating the ice chips..no worries as the NG will just suck it right back out...lol. BUT the chips will stimulate more gastric acids...

I, too, got Dilaudid IV for most all 50 days....whoohoo. It would make me so loopy, within seconds. The nurses got so much laughter once I was "drugged". LOL.

Otherwise, at least she has pain under control Has NG to empty tummy and got ice chips, so all is good, yes....at least control over some of her problems....hugs buddy!