Published
Will they be inserting an NG tube? If they do that, it will most likely be temporary. If it were to be long term, they would need to do a gastrostomy and put a tube right into his stomach or intestine (jejunostomy..I think). Why don't you just ask?
Like 3rdshift said, he will be able to get all of his nutrients this way. They will pump enough into him to get his strength back and hopefully come home soon!
Kristy
thanks very much for all your help guys. He actually got the tube put straight into his stomach. This all happened so fast no one has really had much time to ask questions and get the info we hoped to have gotten. We were told he needed the tube Tuesday afternoon and it will Wednesday (tpday) at 11:00 that they did the surgery. Our heads are all still spinning from the news. For right now the tube is a long term thing but eventually he might be able to gain the muscles back to swallow and he can have it removed. Once again thanks for all your support and help you guys are so great.
Kimberly
Very sorry to hear about your fiance. Give our best to him. Is he on a continous feeding, or is it bolus? What type of nutrition are they using? Sounds like eventually they will try him out on thickened liquids and pureed foods. If he can tolerate that well, he will move up. Takes time, I know, but have patience. Pneumonia with complications can be quite a battle. But, it appears he's on his way back. Good luck.
well I just thought I would update everyone on what has been happening with my fiancee. The hospital let him go home on x-mas eve even though he was not cleared of his pneumonia. Things were not getting better at all and at 12:40am on Friday December 27th he passed away at home with me and his family by his side. He was not strong enough to cough it out and it finally filled his lungs up until he suffocated to death. Even though I miss him already I know that it is what's best for him. He is no longer in pain and suffering and can finally live a normal life in Heaven.
Kimberly
Wannabe RN Kim
12 Posts
hey everyone,
This is only my second time posting a message on this site but I visit it regularly. I'm not yet a nursing student (hoping to be excepted next Sept) so I've never really had anything to post, but today I got some bad news and would like some input. My fiancee is in the hospital for pneumonia and was told today that he will need a tube feeding put it because the flap that covers your airway when you eat is not doing its job. This is devastating news because he also has NF2 which has rendered both of his arms and legs to be fairly useless.
I was just wondering if you guys had any info about tube feeding you'd be willing to share and any thoughts or sugestions. Any help given would be greatly appreciated. You guys are a great bunch of people!
Kimberly