Mom was given the ng tube when in the hospital for surgery. While she was there she did fairly well with her feedings, she had some gastric issues but they seemed to pass. Since she has been home she has been getting sick to her stomach halfway through her feedings. I have adjusted the volume to try to have it go slower but it still seems to make no difference. Is it possible that she can't handle the nutren? She had it the entire time she was in the hospital. I worry that maybe I am missing something here.
The visiting nurse doesn't come back till Thursday next week. We meet with the surgeon, ro and mo, Mon., Tues, and Wed.
Other than that issue she is doing fantastic!
Will update on her more later. Any help about her feeding would be greatly appreciated.

Donna, I had the same issues when I went home after my first surgery. I started being sick to my stomach with the tube feedings. I chalked it up to me being more active being home than I was in the hospital. I started trying some different types of foods and found that the Walgreen brand liquid food suited me best and it saved me money! I just started using my new PEG and had that sick to my stomach/headachy feeling tonight. I hate it!
Take care,
Minnie

Hi Donna,

We are using Bill's PEG exclusively for feeding although the last few days his throat is way less sore, so he is drinking water and Gatorade by mouth. His script calls for 6 cans of 1.5 Nutren with fiber a day...a hard amount to get in him as he can only tolerate 1 can at a time. The first feeding (gravity) in the morning is his roughest...he gets a "flush" and slight nausea and has to sit still for at least 1/2 hour to get over it. We learned that he needed to shower and get dressed for his AM rad treatment before each feeding to allow time to just sit afterward. Each feeding during the day gets easier but it still is not perfect. I make sure that he gets at least 10 ounces of water with each feeding...seems to help all the way around and provides hydration...almost two quarts a day if we make all the feedings.

We have not tried anything else...this is what home health (insurance) provided us and we have stuck to it. I would a)give it a little time..b)add plenty of water before and after the can...and c)make sure she is still for a little time after feedings.

None of the nutritionists at the MO/RO had an answer for the "yuckies" after the Nutren...acted as if they had never heard of such...go figure. So, we have just toughed it out.

1 More treatment day left and we are done! Yea!

Good luck, Deb

The sitting still for a while after thing is really important, especially when the PEG is new and her stomach isn't used to it yet. If necessary, you may need to do half a can, in a slow drip form, at a time, let her rest, then give some more. That's what I had to do when my stomach was at it's queasiest! The other thing is to experiemnt with how she is sitting when she gets fed. Either stitting too upright or leaning too far back during and after tube feedaing can make it harder for the stuff to get through the stomach.

Nelie

Thanks!

Today's feeding went miserably. The machine continued to beep, she was hungry and couldn't get the nutren in...turns out that her dobhob is broken. I am vrey fortunate to have a friend across the street who is a medic in the army. He came over to aide me in trying to figure out what was happening, we tried flushing the line through and came upon the clog. He was so patient and continued to work the line. Finally we heard a pop. Mom said she could taste something, started to gag a little--saline. Called the ENT on call, fortunate for us, he met mom on Friday and said to give her her meds by mouth.
I hope that they remove the trach and tube tomorrow. She is so hungry. No food tonight, not even that delicious nutren. I hate the smell of it, it reminds me of baby formula....my older daughter got sick and spit up--projectile in my mouth!! 17.5 yrs later and still gag at the memory.

I'll share all the info above with mom, it helps so much to know it's not just us.

Donna,
I hope for your mom's sake and your's too that the tube comes out soon. Sounds like she is having an awful time. My mom could not tolerate Nutren. She did best when she first started on Jevity. My guess is that, based on everything we tried, the Nutren might not have enough water in it as part of the formula, or else the fiber may be filling her up too much. My mom has had her tube for 4 months now and tolerates the feedings well, although still vomits every once in awhile if she has a lot of mucous and starts a coughing fit right after eating. Overall it was a lot of trial and error, but maybe the Jevity would help??? We also use Carnation VHC to cut back on the volume required for some feedings. My mom takes in a lot now - 2 cans of Jevity twice a day and one can of carnation twice a day (a total of over 2,000 calories).

I hope this helps. Send me a message if there is anything else I can do to help. We have been through the clogs, the vomiting, you name it!

I hope your mom is doing well. Sounds like, given all that has happened she is really doing a great job, as are you.

Amy

Hi Amy,
Thanks so much for your help.
Feeling a bit lost at the moment, she is so hungry and the appt with her surgeon isn't until 1pm. I know she could handle something to eat by mouth, but can't allow her to do it.

Where are you in NJ?

Donna--will be thinking of you and mom at appointment--hope all goes well for you both,

Brenda

I also use the Nutren 1.5 with fiber. What I do is dilute it with water and then run it through the tube. I mix a can of Nutren with 300 cc's of water and then run clean water through my tube when I am done to clean the tube out.

Billy

Thanks Billy.