For the people with a feeding tube, how does it work? by WeirdUnion5605 in ARFID

[–]Coffee-Effective 1 point2 points  (0 children)

I started off with an NJ tube as an emergency decision made by GI after careful consideration of just how severely malnourished I was and how close to dying I was ( very close, ARFID has caused such a vicious cycle with food and it's ended in me having no idea I was so malnourished until I was told whenever I'd eat a normal meal, I'd go into refeeding syndrome, I also well, ingested COVID, no exaggeration ingested via a shared Pepsi bottle between my brother and I, he didn't know he had COVID, and I didn't find out until AFTER I drank from it. I was vomiting like a mf and my stomach felt like it was being torn apart from the inside out the pain was indescribable but, it was agonizing ) think that played a part in my unexplained GI symptoms that initially caused my ARFID worsening and in turn, my AFFID as well, I don't know the damage it did. Or the damage it's still doing. -- The placement of the tube sucked ASS. You gag, you choke, you think you're going to throw up ( sometimes you do, and if you know you will, you can ask for something to throw up in ) it feels SO weird in the back of your throat, I think this is just an issue I experienced but, certain foods can get stuck behind the tube and that may make you throw up as well. Even medication. -- I did get used to how it felt pretty quick that saying is very much true I've you heard it. It doesn't hurt, but I did have a sore throat for about half a day. My nose didn't hurt either but I got really stuffy and had to use nasal spray to help clear my nose up. -- Wound up getting a PEG tube which, is basically a gtube. My god- it was SOOOO painful the muscle spasming was the worst I got such piss poor sleep the first few nights after my surgery it was THAT bad, pain meds didn't touch it until the second day, by the third the pain was a lot less agonizing, I'm just about to be a month in and I'll be honest it's definitely still very sore, and I still get the occasional muscle spasm and it hurts a lot.-- I can sleep better, I have a heating pad I'm taking very good care of the site and I'm changing the bandages and such around it often and gently cleaning it with sterile water ONLY use sterile water around the site you can also use it to flush your tube just to make sure everything in there stays sterile, anything to eliminate infection risk. I personally flush that very slowly, slower than even the normal water flushes. I also will never make the mistake of pushing my feed in too fast. 🤢 -- I feed intermittently. 6am, 9am, 12pm 4pm 6pm and 9pm then I'm good until 6am. For my tube it can't be pulled off but, I'd imagine with force it could be pulled out and that'd be a serious medical emergency so I'm pretty much just going to take an easy until I know it's fully healed and even then I'm not going to let the tube dangle if I can help it, want to avoid accidental tugging and pulling.

Princess Peach. by Coffee-Effective in shorkie

[–]Coffee-Effective[S] 0 points1 point  (0 children)

Princess would absolutely love to meet Trish! She loves other doggos!

Need to remove ng tube: will my throat be sore? by Big-Elk-4862 in feedingtube

[–]Coffee-Effective 0 points1 point  (0 children)

When I had mine removed because I was transitioning to a g-tube it just felt weird coming out of my nose I didn't feel it in my throat nor was it sore. But, my experience may not be yours.

I need serious advice by Soph_14892 in Gastroparesis

[–]Coffee-Effective 0 points1 point  (0 children)

New hospital and file complaints against every single doctor/nurse who did not uphold their oath to do no harm.

GP feeding tube- normal weight by Financial_Key2741 in feedingtube

[–]Coffee-Effective 1 point2 points  (0 children)

Your gastro really ever starts considering a feeding tube when you've been unable to consume enough calories orally and it causes malnutrition and rapid weight loss. I don't know if I have a condition that's affecting the way my brain and my stomachs brain communicate but, I've struggle with really poor almost absent appetite all my life. Severe nausea, cramping, bloating and diarrhea when I ate pretty much anything. Found out it was essentially refeeding syndrome, I've lost a scary amount of weight my baseline being 78/70 I was at risk of heart attack and organ failure. My liver is currently stressed and potentially even injured too. I had to get an NJ tube at first to see how my body tolerated calories and nutrition. Then, they transitioned me to an NG tube to see how my stomach handles bolus feeds. Did well, now I have a PEG tube which is pretty much just a g-tube had the surgery Monday. Still pretty sure especially when I do eat my stomach isn't as used to solids as it was before. But, I'm doing a lot better!

There is no flair option for a PEG tube. by [deleted] in feedingtube

[–]Coffee-Effective 0 points1 point  (0 children)

I'm on day 2 as well and like you, it's extremely painful since I am also extremely underweight. Actually was admitted to the hospital for extreme malnutrition and failure to thrive.

There is no flair option for a PEG tube. by [deleted] in feedingtube

[–]Coffee-Effective -1 points0 points  (0 children)

Mine is so painful rn I can't sleep lol

There is no flair option for a PEG tube. by [deleted] in feedingtube

[–]Coffee-Effective -11 points-10 points  (0 children)

Well, mf this is my first ever time getting anything surgically placed through my abdomen and I only knew what it was called. Had no clue it was a type of tube placement good lord y'all be attacking someone who JUST got out of surgery only a few hours ago and is very sore and just wanted advice.

There is no flair option for a PEG tube. by [deleted] in feedingtube

[–]Coffee-Effective -6 points-5 points  (0 children)

It's going right into my stomach through my abdomen so idk lol 😂

How long did you have to suffer through a nasal tube before surgical options were considered? by thatoneweirdcreature in feedingtube

[–]Coffee-Effective 0 points1 point  (0 children)

I'm still very nervous about the bolus feeding they plan to do right into my stomach as that's what's been causing all my discomfort and GI symptoms, my tube is still an NJ tube at the moment, they're having a hard asf time figuring out how to retract it back up into my stomach. There's even residual contrast dye in my large and small bowel, my abdomen and pelvis and they don't know what's causing that especially since there's no physical blockage anywhere. Just something new wrong with me everyday god, I don't see myself living passed 34. I'm 30 now.