Hello,
I was wondering if anyone has gone through Nissen Fundoplycation surgery? I am 22 and have been suffering for several years from severe GERD and IBS. I was finally diagnosed in November and am having the surgery next week. What can I expect in terms of
recoveryRecovery position - series, did it work. . . ?
Any information would be greatly appreciated!
Thank you,
Kate
I'm not sure if that 24 hour-ph question was directed to me, but I'll answer it anyway! My test results showed that I have very high acid, I don't know numbers, but were they found the most informative result was from the esophageal manometry, the first test once the 24-hr tube is in place. It tests the pressure on the swallowing tube. I had 0% pressure which was causing the regurgation and severe acid.
I'm young for the surgery, but as I have been suffering from this for just over two years and my system is showing serious signs of damage (holes in the esophogeus, tooth and gum damage, weight loss, asthma and now irritable bowel syndrome) my gastro doctor, the surgeon and I have decided that I really am an excellent candidate.
Thanks again for your quick response.
Kate
I feel I need to tell you my story of the events before and after my surgery. First I have to say that my results do not necessarily reflect the outcome of the majority of patients, although I also am searching for help online to see if anyone has been dealing with what I've been going through since my surgery! First a little background info about what led me to having the surgery. I am a 44yo female. I suffered from severe heartburn for years.It led to esophagitis with ulcer formations, I suffered from aspiration pneumonia,I had such severe esophageal sphincter tone that if I bent down at times I would reflux stomach contents out my nose and mouth. I found some significant relief from prilosec for about a year. I had the 24 hour Ph probe,UGI etc, and finally had the surgery. The surgery worked great....no more heartburn(until recently its coming back). I ended up with a surgical hernia, which I've had repaired once so far, which came back and need to have it repaired again, but cant right now because I'm too ill and weakened from the dumping syndrome caused from the surgery!
( I dont want to take up a lot of time explaing what dumping syndrome is but you can go to GOOGLE. com, and search up "dumping syndrome") As far as I have been told their is no cure for it. Oh well, after my surgery I felt pretty good except for a little nausea and occasional diarhhea. I weighed 226 lbs when I had my surgery. I began losing weight almost immedietly but didnt think much of it , it actually was wonderful to be getting my weight down. The problem is I got more nauseous,lost my appetite as time went on.I have abdominal pain which gets worse when I eat,I'm to the point of having to force my self to eat and even keep my fluids going. I'm down to 145 lbs and no end in sight. Please dont think this sounds like a great weight reduction cure... because it is literally probably going to kill me.....I feel so weak from all this, that I feel like I'm dieing slowly.I'm a nurse and was at work last year and past out from this, ended up with a concussion and neck injury. The other night at work I had to leave and go to the emergency room to get IV fluids because I was so dehydrated. They did orthostatic blood pressures on me(thats where they take your BP and Pulse laying ,sitting, standing)and I passed out. Luckily I didnt get hurt.I have bad veins and when I get so dehydrated its even worse to find a vein.I'm soon going to need to have a mediport put in for IV access,and most likely will have to have a feeding tube put in because I just cant get enough food and fluids in to me because of the severe nausea.
My Doctor never told me this could happen, I since foud out through research that a small percentage of patients can end up with this dumping syndrome. It's the vagotomy part of the surgery that causes this. So please talk to your surgeon about this. If I had it to do over again I might have had the surgery,but told him not to do the vagotomy(a vagotomy is where they cut some of the nerves to your stomach that help you secrete stomach acid to help in digestion). I'm sure all I needed was to have my esophageal sphincter tightened up to prevent my stomach acid from coming up my esophagus and throat.
I am so disabled from this that I will have to go out on disability very shortly.
If anyone out there wants to e-mail me to talk about this feel free. my email is ***@****, also I would love to hear any one elses experience with this and if your going through what I am!!! Thanks for listening and good luck,
Marilyn
PS you might want to print out this letter and show your surgeon before you go through with it.