Post-Nissen Fundoplication Problems: What helps?
I had a nissen wrap operation in 1999. I still have problems at night after about 4 hours of sleep. I've tried all kinds of drugs to help relieve the gas. Right now I am on 40 mg of pantoprazole in the morning before breakfast. Most of the time days are fine. I have problems being regular on bowl movements, so I have a high amt of gas from the meds I take to go number 2. At night is when I have real problems. Any kindred spirits out there?
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I don’t know where you live but Dr Parkman at Temple Hospital in Philadelphia specializes in gastroparesis.
I'm so very sorry to hear about your grandson, very difficult to watch. I DID have 2 gastric emptying studies, one showed food in my tummy after 18 hrs. of no food, the next one was negative.
I am considering asking my GI provider to order another one, since I do feel I'm not digesting food properly at all. But since I just had brain shunt surgery, I think I'm going to wait a bit to get the study done. Thank you so much for the warm wishes! Much appreciated!
I had a 360 Nissan done in 2007 at Johns Hopkins. The wrap was way too tight. I had several balloon dilations over the next few years and finally had a revision of the Nissen to a 270 wrap performed by the same surgeon. A year after the first Nissen I started to gain weight which I desperately wanted to do; however, I also had new GI issues including a a growing stomach/abdomen that was rock hard, severe constipation (prior to the surgery I had IBS-D), and nausea. The 270 didn’t do much - I still get esophageal spasms, food gets stuck where the wrap is, & I have to take reflux meds bc food & liquids come back up into my mouth. Over the next 2 years my stomach got increasingly bigger, I was in constant pain, & I barely had a bowel movement and it got to the point where I didn’t have any. The rest of my body started to puff up and I looked like a pregnant pillsbury doughboy. Ppl would often ask me when I was due and there was woman on the street who said “you must be having twins!” I would just give a smile and move on. After the head of GI at Johns Hopkins called me a conundrum and seeing other GI specialists in PA, I got an appt at the Mayo Clinic in Rochester.
I found out there that I had vagus nerve damage, gastroparesis, & that my colon had died (and that I had been walking around w/ a dying colon for years) & that I needed a total colectomy.
I was thrilled that they figured out what was wrong and “how to fix it.”
Things aren’t great by any means GI-wise right now BUT it’s a million times better than how I was when I first got to Rochester.
I actually saw Dr. Parkman at Temple Hospital right before I went to the Mayo Clinic !!! (Probably 2-3 months before)
Unfortunately, after spending a week living out of a hotel room in Philadelphia and seeing Dr. Parkman for an appt, had the tests he ordered performed, and an appt to get the results he did not have anything new to tell me. He just read me the results that which he said were all normal and that was it. After asking him if he had any idea of what may be causing my GI problems he just said no- he offered no guesses, other possible tests, or doctors that might be of help.
I’m so sorry. I know that several people praise him.
Why do I still have painful GERD after Nissen Fundolpication?
Almost 3 years ago I had the surgery it was difficult and long recovery. Nothing changed regarding my symptoms. I tried Voquenza which helped greatly for a while. I went to the Dr. who asked me if I wanted him to stretch my esophagus again.
That had not helped prior.
Recently the GERD has gotten worse. I feel like I’m just waiting to get esophageal cancer that I’m just alone that no one could care less. I have a referral from my primary somewhere else. It is hard to get through the night. I feel like I’m choking, pain in the stomach and throat it’s awful. My Gastroenterologist gave me no options. Advocate for yourself because no one looks out for you as a patient.