My Laparoscopic Nissen Fundoplication Experience


Sep 17, 2015

I had the LNF surgery three days ago and just wanted to tell you my experience of it all as I was terrified of the surgery and of the side effects afterwards - so much so I considered cancelling it at the last minute! I read a lot of information on the web in the days leading up to the surgery (good and bad) and was left feeling that even people with what seemed to be good experiences seemed to be having a very hard time. As it is so far I've been pleasantly surprised!

I had surgery due to a loose gullet which was confirmed via endoscopy. I opted to not be sedated so I could get the results these are then (if you're sedated you get them a few days later as you tend not to be awake enough afterwards to take in the information). The endoscopy wasn't the most pleasant experience but was over fairly quickly and something I could do again if needed without being nervous about it.

I then had all of the PH testing which confirmed acid reflux and the associated tests for swallowing that confirmed that I was a good candidate for Nissens.

Fast forward to three days ago and arrived at the hospital very nervous about it all and feeling like I wanted to back out. I'd read information on the web about bloating, not being able to burp, not being able to vomit, dumping, diarrhea, etc. and couldn't see how I could live with all of that afterwards! My surgeon was very dismissive of most of my fears (in a good way) and confirmed that not being able to vomit may be a side effect and short term bloating may be an issue but the rest of the side effects won't be an issue. I really trust the surgeon as he has always been very open with facts and statistics so was happy to go ahead with the surgery.

Feedback from the surgeon was that the surgery was very straightforward. He found a Hiatus Hernia which hadn't showed up before which he fixed as part of the fundoplication.

Since the surgery I've had a lot of discomfort in my tummy area but I've put this down to the holes that were made for the procedure rather than the fundoplication as it is very localised on the surface of my tummy. My lungs have been a bit sore since too and breathing in deeply has been uncomfortable but both issues have eased over the past three days.

In terms of eating and drinking I'd been told by the surgeon to experiment with textures to see what I can handle which is much better than the clear fluids for a week I was expecting. So far I have been able to drink water, squash, Horlicks and Decaf coffee without any issues. It takes a lot longer to get through a drink as there is a feeling inside like a funnel where liquids get backed up a bit when I swallow too much but there is no pain associated with this and it goes away after a few seconds. I managed to each half a bowl of Weetabix the morning after the surgery, moving on to custard, semolina and chicken soup over the past couple of days, none of which was strained. I'm probably not drinking enough due to how long it takes but my bladder and bowel movements are pretty normal so I'm not too worried about that at this stage. Also I am able to burp after eating and drinking. Probably not voluntary at the moment but when my body feels like it needs to it does. The same goes for passing wind too although there seems to be a lot more of that than usual!

So far I have no regrets about the surgery and feel that it was definitely the right thing to do. I expected the weeks after the surgery to be difficult but so far haven't suffered too badly. I'm self employed and work from home on a computer and am aiming to do a few hours this afternoon building up to full-time again next week, one week after the surgery. However, if I wasn't working from home I don't know if I could manage working in a office at this stage yet and definitely couldn't handle a commute via car, train, etc.

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I have very large fibroids, and I've been offered a few options by different doctors. The first surgeon I saw recommended open surgery. The risks associated with major open surgery are serious. The first, and biggest concern, for me is the risk of waking up without a uterus. I'm quite attached to my uterus. My second concern is the amount of time I'd be out of work. I freelance, and my job is very physical. I will not be able to return quickly, and I don't get paid time off.

I was not on any type of insurance when, March, I found out the problems I'm experiencing are due to fibroids, so I went on Medicaid to pay for medications. Several doctors have recommended that I go on Lupron, which is $800 to $1,200 a shot.

Being on Medicaid, I'm fearful that I won't get the same level of treatment post-op. A few nights in a hospital charity wing can be deadly. Let's face it.

I went to get a second opinion from a doctor who referred me to a the head of robotic surgery at the hospital. She told me my fibroids can be removed laparoscopically. I researched the procedure, and the surgeon I was referred to, and I'm on the fence about what I should do. The surgeon would need to break up the fibroid in order to get it out, and when the FDA began discouraging its use she was quoted in an article touting it. "It needs more research." Well, I'm on public assistance. I'm on public assistance and I'm not stupid.

I'm between a rock and a hard place here, because none of my options are good. Morcellation spreads cancer in 1 out of every 350 myomectomies, which is why the machine is being recalled.

Do I take that gamble? Open surgery sounds terrible, and it will set me back for a long time--and that's if everything goes right! So should I risk laparoscopic surgery and hope that I get on with my life safely, or do I get the traditional major surgery? My friends and family are pushing me to get a laparoscopic myomectomy but I have reservations. I've also been exposed to a lot of chemicals, because I'm a painter. I've since been more diligent, if not militant, about safety and protection... but exposure is exposure. I worry about it. Certain types of cancers do run in my family, ovarian, uterine, cervical, etc. not being among them. Other endocrine related cancers do run in my family, along with diabetes and endocrine conditions not related to cancer. My mother had endometriosis, and both my mother and sister would get ovarian cysts. I, however, do not.

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I hope you don't mind me posting on here a rambled question as I'm new to the forum and haven't contributed yet. I've read through several posts about Laparoscopic Ventral mesh Rectopexy and some not so positive outcomes, and my heart goes out to you all!

I had the LVR done nearly 6 weeks ago. I have had chronic constipation for 7.5 years now and have only just, this past year, been able to get anyone to take me seriously. I'm now 26, and have been through everything in terms of diet, water, exercise, toilet position, relaxation, supplements etc. I have been on Dulcolax daily; things like Senna or Movicol don't seem to do anything, and newer drugs like Prucalopride have been useless. I paid for a private consultation in Oxford follow my request to my NHS gastroenterologist for a transit study and defecating proctogram. I had a rectocele and intussusception grade with with full rectal prolapse. 

On a side note, I have pernicious anaemia, folic and iron deficiencies, and was recently diagnosed with Hypothyroidism (after a lot of pushing!). I am being treated for all of these but the Levothyroxine for hypo isn't doing anything, so the GP has suggested some people look online for an alternative NDT...

Post surgery, I've been constipated as usual. The Movicol / Laxido did nothing on 2 sachets a day. 3 sachets a day and nothing happened either. Dulcolax did something, but it didn't work as quickly or as effectively as it did prior to surgery. Last week I called the consultant and he suggested I may have impaction and to take Citramag. I've done that this week and it was horrendous - 2 sachets and 8 hours later, and I was finally able to go. This was mostly with pushing my stomach out, massaging my stomach, moving around etc.

I feel like there's still some kind of obstruction because with laxatives I know there's something in the rectum, but it goes no further. Without laxatives, and I don't feel anything there; it's like nothing happens in the descending colon, there's no 'activity' that I can feel. Before surgery, the transit study showed all markers still in my colon as I didn't move my bowels at all. The markers were mixed, some made it to the rectum but many were at the top of the descending colon. I'm wondering whether it's possible I'm still 'obstructed' and whether my colon is even working (all these years having to take a stimulant laxative surely won't help!)

I was just wondering whether anyone has any thoughts? I'm exhausted, just spent all of the money I had to my name on this surgery and I feel like it's worse. I should have been looking to go back to work from next week but that's not going to happen with the state I'm in. I don't want to be on laxatives, and I feel these past 7 1/2 years have been a complete waste. It all seemed to happen over night that I became constipated as I'd never had any problems with my digestion before that (I was prescribed iron tablets and thought it might be those, so I stopped taking them but never regained bowel function). 

I see the surgeon next week but don't know what I should be asking or what options I should look to explore. I can't go on like this and I'm sorry for the rambling and feeling sorry for myself, I'm just feeling very alone right now and pretty fed up.

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Five hours now and I feel good but I can hear everything around me, the talking , the tv, things very far away are very clear. My dog barked right beside me and I nearly jumped off my chair, scared me. It was loud. I used to watch tv on 65 volume now it's at 40 volume.

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I think there are three major factors that contribute to the outbreak (environmental, mental, and diet), and I'll explain each in more detail:

Environmental: During dry winter seasons, I develop skin rashes all around my body (guys hate lotion), I think if dry skin can contribute to skin rashes, it probably can contribute to pompholyx outbreak as well.

Solution: Make sure your body is well moisturized, I really don't enjoy the oily sensation, but it sure beats waking up to the itch in the middle of the night! Cetaphil cream (not lotion) work very well for me. Stock up when they're on sale!

Mental+Sleep: I was unemployed when the first episode occurred, and I think stress has a lot to do with it. Also, make sure you sleep at least 7 hours a day, and try to relax and think positive thoughts as much as you can.

Solution: I just try to be grateful of what I have... there are people out there who are suffering diseases 1000x worse than pompholyx or being unemployed....

Diet: The dermatologist told me to cut out chocolate and nuts (especially peanuts) completely. It was HARD. But I started about 2 weeks ago, and it's been working so far. There was a scientific study about the possibility of chromium in chocolate that induced a flare up (from breast milk)

http://www.ncbi.nlm.nih.gov/pubmed/17671414

For nerds like me, you can check it out (be aware though, it's just a sample size of 1!)

solution: see above, you can cut out coffee too, but that will be too hard for me.

Medication:

As a prophylaxis, I take a 180mg fexofenadine every night. In addition, when you see (or feel) small blisters starting to accumulate, there are two topical steroids that I use.

0.05% clobetasol propionate (GSK markets it as Dermovate), ointment form

0.5mg/gm fluocinonide, cream form

http://img.medscape.com/fullsize/migrated/551/352/dn551352.tab4.gif

clobetasol is listed as class 1, very high potency steroid, and fluocinonide is listed as class2, high potency steroid. My dermatologist assured me that applications to the extremities (fingers, toes) will not cause a lot of absorption to the body, so you can be very generous in your application.

I also take multi-vitamins. My dad (who's an MD) told me Asians do not absorb B-vitamins very well, so it's important to supplement with either B-complex or B-12 vitamins.

This is a pesky condition to have...

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Wouldn’t  the ultrasound identify these if any? Has any of you done this test (Flexible Cystoscopy)?

Does any of you managed to have an Antibiogram test (or ABG)  which allow to identify what antibiotic is right for that type of bacteria?

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It's always fear of the unknown which scares of most. After the procedure the only pain I really experienced was wind as they had probably pumped the world's gas supply into me (ok so I might have exaggerated a bit) but seriously, it's not all that bad and you'll feel ok right after one big release.

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Most of these things I thought were just normal women's behaviour, but after speaking with many other women who have since gone off various other contraception, it has been brought to my attention, this all might be a side effect.

I have not had a period since having it inserted -except when it was removed after the three years while waiting to have it inserted again- which has been great. Despite this my main concern are the constant headaches, so I am having it removed and staying off contraception like this for a while to see what changes may occur.

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Experience With SI Joint Injections?

Anyone have experience with SI joint injections?

I have been dealing with pain (from nagging to disabling) for almost a year. A year ago, the pain slowly progressed to the point that any position was uncomfortable...sitting, standing, walking, sleeping was impossible (for some reason the pain seems worst at night). At that point, I called my spine surgeon (had a lumbar burst fracture 5 years ago so already had a doctor ), but the first available appointment was a month out...I scheduled the appointment and went to the ER after not sleeping any more than an hour or two for several weeks in a row due to pain. They gave me a Toradol injection, muscle relaxers, and Vicodin. I went home thinking that I would finally sleep...WRONG! All those drugs did nothing to stop the pain! I struggled through the next few weeks until my appointment. My doctor's first guess was a disc problem due to my history; however, MRI showed healthy discs and fracture site looking as good as a burst fracture can After a few more tests, he diagnosed me with an SI joint problem and put me on Relafen for 6 weeks to control inflammation. After 3 weeks, I did see improvement...The pain returned to the "annoying" level. Since that time, the pain has been up and down...Always there, not always awful, but sometimes miserable for weeks at a time. I had a foot/ankle reconstruction in November and had a HUGE flair up after that...I realized that I really had an issue when my back pain was keeping me awake at night, not the heel bone that had been sawed into three chunks! I was hoping this problem would just disappear as mysteriously as it began; but, unfortunately, it looks like it's here to stay. My doctor has recommended an SI joint injection as the next step.

Has anyone had success with SI joint injections? My typical symptoms are left side lower back, hip, and thigh pain from just annoying to feeling like my bones are disintegrating...that's the best description I can come up with I also have a lot of muscle soreness in those areas.

How was the "injection experience?" I've had cortisone injections in my foot before, and they were not pleasant...So, I'm definitely not excited about this. I have a high pain tolerance and have dealt with a lot of medical procedures, but something about someone sticking a big needle in my back doesn't give me a warm, fuzzy feeling.

Did you have increased pain for a few days following the injection? After the ones in my foot, I had fairly severe pain for several days...I think they called it a cortisone flair.

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Hemorrhoids :: My Experience Of Haemorrhoidectomy

Day 0.

Scheduled to go to the hospital at 7:30am. Booked in no problem, just thirsty from lack of water. Was no.3  on the list so went into theatre at 11:30 ish. Nice anaesthetists, no issue with the general being put in. Drifted away quickly it seems. Only bad thing was th surgical stockings they made me wear, clashed with my gown.

Woke up at 1:30 with a really sore throat and blocked nose and ears. Side effects of the general it seems. Bum was a little painful at this time. 2:00 moved to recovery room, still feeling a little sleepy. Had some water and he a nice cuppa. Had some bread and butter (they wouldn't let me leave if I didn't eat). No problems with the waterworks but did feel the need for a poo or pump. Nothing came though, no straining!!

Had an ibuprofen with the tea as felt pain. 30 minutes later it must have kicked in, as it was a dull throb then. Tried to do some puzzles in my book but kept dozing off. Nice nurse kept coming in to the my BP every so often and changed. Dressing when a bit fell out. Had a wander round the ward and got dressed. No problem walking, through balance was a bit wonky at times. Wife collected me at about 5 ready to go home.

Got in, had another pee. Opened get well box of presents, had a drink of tea, snarled some of the kids scampi and had a weetabix laced with flax seeds. Drinking lots of water,ergo peeing a lot and sitting on a hot wat bottle to relieve urge to poop. Took a codeine at 5 as well as a paracetamol and antibiotic, next set of Meds is about 10ish.

pain rating 3/10. No worse than a bad day of haemorrhoids at the moment.

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Hemorrhoids :: My Experience Of Surgery

My name is Gary. I am 57 and have had problems with hemorrhoids for years. It was getting to where I was spending two weeks out of the month basically ok due to constipation from opiate medication I have to take. Then one week where I use the prep H to push the roids back into place. Then often a week of just pain, stool softeners vs pain killers, and out of service.

I got referred to a surgeon recently and he said I had a bad case and set me up for surgery. They decided to do a colonistmy (colon probe. where I guess they pump you full of air and put a tube all the way up). I did not know that it was that extensive or I might of gone without it..at least not with this surgery.

I was told afterwards that I had some of the largest they had seen. Also the colon test showed some polyps they had to burn out. They did not look cancerous.

I had trouble getting cleaned out prior to surgery due to the pain and the opiates. As required I took 250 grams of miralax stool softener, 4 laxatives, and waited. I took them at 4 pm, had surgery lined up for 8:00 am with a 6:00am arrival. The drugs did not take effect until 1:00am so I was up until we had to leave for the hospital still on the toilet..and in severe pain.

I was still eliminating when we arrived. I was given a couple of ememas to use on myself. I couldn't hold them but they came out clear so they started the surgery, colon probe, and prostate exam.

I awoke after 2 hours of surgery. I was still under the anesthesia (I was put out) and not in terrible pain. I got up and was able to urinate. I had packing in me and was told to go home, take a bath, and they would come out. I had terrible cramps and gut pain, prostate pain, and severe anus pain. I have lots of stitches down there.

I went home and ate a small bowl of cereal and some oatmeal...and waited. I drank a bunch of juice and water but could not urinate. I was leaking blood everywhere. I took several baths and finally the packing came out. I took stool softeners and drank a lot. Finally the first meal, or what was left over from before, came out in the bath. I didn't have a full bowel push because of the pain but a bunch of crap, in small strings, some packing, and a huge amount of blood came out. I would say a pint.

I ate some more: a bacon and cheese bagel, some oatmeal, and stool softeners. I drank a bunch. I also had to take a bunch of painkillers. One the  third day I had an involuntary bowel push but came up empty. I couldn't take the pain. Blood was still coming out in drips all the time with a small amount of feces. I called the doctor and got more pain killers. I set up a plan last night to have a bowel movement this morning. I ate some more oatmeal after one day without food. I took several sleeping pills and some painkillers to stop the urge to have a bowel movement. I had to get up at 12:00am and take more pain killers to stop an early bowel urge which would come up with nothing as is my experience. I awoke at 7:00am, as planned, and held the pain killers aside. I forced a bowel movement and produced a large pile of soft serve sh*t which was full of blood. There was more to come but, now 6 days out, I was in too much pain to push again.

It becomes a real fight to live. I am addicted to painkillers from years of degenerative disk disease and arthritis due to an 80 foot fall in 89. I don't get my refill until the 13th which is 3 more days. I have enough for today. I have stayed away from the long acting painkillers unless I run out. I hope to pass more later today. I will probably try the same procedure.

Again, it is the sixth day, and I still cannot walk without using the furniture. I try and move around as much as possible. I have some blood a fecal leakage which I clean up each time with a bath or a soaking wet warm wash cloth. Then I fold a washcloth in half and put in between my swollen cheeks until dry. They shave you down there and the stubble that grows back is very painful to the opposite side. I have never felt such pain. Each day has been a little better except for the third in which I was worse. 

I would've still done the surgery if this all turns out ok. I will eat better, drink more, and do whatever I have to do to keep this from recurring.

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