Gallbladder is gone so where is this pain from?

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HI

Had the dreaded gallbladder removed last June after only 7 months of pain (so I'm pretty lucky).

Everything went well, home the same day - took a good 4 weeks to feel totally better after the op but eating was ok and I don't seem to be affected by bowel issues like some people.

Only problem is I have dull ache in exactly the same place I used to get the gallbladder pain. It's not intense pain but it's in the front RUQ under my ribs and moves round the side and to my back.

It doesn't seem to appear after anything in particular and most of the time it's there constantly. Suppose it's more of an annoyance than anything else because I'm always aware of this ache. I'm quite reluctant to go to my GP because after spending about 7 months constantly in the surgery last year updating painkillers and nausea pills I don't want them to think I'm addicted to medical attention.

Just wondered if anyone had anything similar or if it's just a by-product of surgery that I'll have to get on with?

Thanks

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  • Posted

    Hi everyone

    Anyone that doesn't suffer gastrointestinal problems constantly day in day out over many years ,doesn't really understand what's going on with us

    I've had over the past 20 years Ulcers, Helicobacter Pyloris (treated 3 times)

    Reflux (just this on its own is enough)

    Esophagitis.Polyps removed Gastritis

    Gall bladder removed,a dozen or more endoscopic procedures.,not to mention sleepless nights intense pain nausea vomiting dizziness and general mal estar and lack of energy

    I'm 55 now and have another scan coming to check for stones in my bile canal

    Oh but you must eat badly are overweight don't exercise drink too much I hear some say

    Well I eat fruit and veggies don't smoke don't drink alcohol (which I recommend to anyone)exercise over an hour a day 7 days a week

    Guess at the end of the day it is just meant to be and I should be just thankful that I don't have something that is debilitating like some poor folks

    Hope you get better soon and we all someday find a solution for our gastrointestinal problems.

    • Posted

      Trust me take one to two tablespoons of raw all natural honey. The real stuff and your pain will disappear in 10 minutes. Works every time.
  • Posted

    Trust me. The best thing in the world for stomach pain after gallbladder surgery even years after surgery is pure raw honey.

    I discovered this after my gallbladder was removed 3 years ago. I tried everything. Even went to the ER one night the pain was so bad. The doctors couldn't figure it out and had no clue what to do. Just gave me pain killers that didn't work. I decided to take matters into my own hands and researched how raw natural honey has been used to cure all sorts of problems. Even the Egyptians thousands of years ago used honey to cure most things. So every time I eat the wrong foods and start having stomach pains I take one to two tablespoons of raw all natural honey. Not the fake stuff at the store. Buy some at a local supplier or health food store. It has to be the all natural raw honey. Keep it on hand just like you would a medicine. After taking one to two tablespoons your stomach pain will disappear in 10 minutes. Trust me it really works. It's amazing! Doctors are just not trained in natural cures and will not tell you this nor even know about this. Try it and save yourself alot of uneccesary pain and even a ER visit. Hope this helps some people out there. God bless.

  • Posted

    So just over 2 years since my surgery and original post on this site.  Sad to say that things haven't improved in any way, same RQ pain same feeling of dripping inside at surgical site, blood feels like it starts to boil moving through my whole body until my brain feels like it's melting, some chest pain.  Bounced from one specialist to the next all with a "take this tablet approach"  I have had every scan, x-ray, blood test prod and poke with nothing showing. Feel so lost as it has impacted my life so dramatically, from the moment that I wake to when I finally fall asleep through sheer exhaustion the symptoms don't leave me.   I used to pedal 350 kms a week, work out, climb and live life, now most days I can barely function and spend the days housebound sleeping on and off on the couch, It's no way to live.  I am frustrated with the medical fraternity as they all seem to have the response of only wanting to mask my symptoms through medication and not actually diagnose what is the cause. On my next upcoming visit I am already aware the tablet on offer is going to be anti depressant / psychosis medications for their side effects which possibly may relax the nerve endings. I don't want to be a medicated zombie so not sure how this is even a consideration. Despite all my frustration I intend to keep on fighting to find a reason why, I want to be healed from this awful journey not just medicated. 

    My heart goes out to all that are suffering as I know the journey can be tough, but don't give up, fight for everyday and be the best that you can be.  Control the things you can, diet and water are paramount, keep a healthy attitude and most of all believe that you can and will be healed.

    C.

    • Posted

      Hay CoffeeCycle22 . PLEASE READ FROM FELLOW CYCLIST – We and many others are identical clones

      I read your post. heart breaking I know, Outdoor exercise freak to : "I used to pedal 350 km's a week, work out, climb and live life, now most days I can barely function and spend the days housebound sleeping on and off on the couch, It's no way to live"

      I'm been living with similar problems for 12 years now post GS. I would like to share with you a support treatment supported by medical opinion.  it’s NOT a cure. Sadly it confirms a simple fact, the gallbladder function in food digestion does more than what we were told "just stores" bile and the “GB not need, can life normal life without it” I’m dyslexic, so please be patient with my writing, likened walking on glass. 

      I’m writing because I don't want to see another two years of your life wasted, with no answers. I lost many years looking for answers, after many DR’s and GI’s I have not received any  definitive treatment or even a diagnosis. There is none, only trial and error and personal extermination around diet. As a result, I lost my career, jobs, income, relationships, every goal in life set. But first some questions to consider:

      -Why are the opinions provided to patients so variable on likely outcomes? On the far far left is the DR's and Surgeons and patient handout information. In the middle is all these people experiencing many post problems I.E testimonies see throughout this forum, patients  receiving treatments that kind of don’t work, no real diagnose / answers received and if you look through carefully many have the same 101 post issues which seem to be around ( IBS, Acid reflux, pain, fatigued, digestive issues ) . And on the far right are the medical studies, evenout of the NHS, all detailing (PCSyndrome ) outcomes , high as 43% woman being affected, chronic and life long and a long list of horrible problems never disclosed from the far left or during problem medical assessments.

      - If the far left opinion is being used by DR during investigations, is this going be a problem and prevent treatment help?

      -Any why is it, if you walk into a Holistic / naturopathic doctor’s clinic, you will receive an immediate answer on what’s going wrong and treatment which involves around diet, food elimination and supplements to aid digestion as opposed to chemical based drugs treating side effects ?

      My share on what helped me recover get well in your exact situation is this: My health failed immediately after my GB was removed. Lasted only 5 months before IBS issues kicked in, stomach pain, Acid reflux (but really bile causing Acid) and massive fatigue and mass / weight gain to boot. I used to do 200 sit-ups every day. I watched this mass slowly take hold before my eyes. At 11 months, had to take extended leave due to fatigue at work.  I always ate a low fat diets (probably why I lost my GB! to single pigmented stone, as I was told at the time remove the GB required). At 3 year mark. Sick in bed, stomach pains, not able to work, lost my job, hospital advising I had not problems, no access to treatment or support would be provided, I decided this was no way to live. Exit planning took place. I decided on a location. Maxed out my credit cards, flew to France for some last rides, my passion for 26 years prior surgery, started cycling very young . Day one:  felt like my heart was going to give out on the smallest climbs, supper scared of peddling hard – heart attack. Day three, with alp d'huez on my left, I rode past the spot Id picked out.  Cut a long story short and to a solution. I kept riding past this awesome high view spot. Over the next week, riding in summer heat, Vitamin D, (liver being flushed out, all the toxins from food not processed being burn out of my body) I started to recover very rapidly. Rode up a hill in pace, (you know ones you can sprint up due to being small and low gradient) without the stomach pain as experienced every time I cycled for over a year. Longer story shorter , at week Six and 3000km under my belt, I found myself cycling around an Italian lake section, with a local rider hanging on for life,  average 35-40km . I was back to normal pre surgery 3 years prior, a very long list of PCS issues flushed out of my body and I can eat anything I liked (everything on the bad list also!!).  Ant the end of that ride I stopped for lunch on the lake side, cried my eyes out for an hour.

      I put it down to, getting more bile out of a flushed out liver to food, food is digested better, nutrients extracted better, body heals. As I said this is not a cure only a root cause confirmation, as soon as I return to a desk job, despite cycling as you normally do in weekends and offer work, the body slowly shuts down. At month 9 I end up having to quit work due to the health issues, in so much pain.  I’ve managed to extend working to 12 months, cycling to work 10-15km + 4 weeks off doing the cycle thing very much helps. So is the Mediterranean and Paleo diet – not a solution without exercise to help bile to food. I found if I did not return, cycled 2 hours a day and NOT seated at a desk for more than 4 hours a day, I can retain my health.

      I’m in France again right now recovering my health again. I fell off a MTB in March. Total immobilized DR orders for 2 months. Sure enough immunity issues kicked in, got sick with flue bugs for another 1.5 months, weight jumped 8KG, massive breast plate of fat kicked in, huge belly, could hardly ride up a small hill with about becoming exhausted, could not breath – more like panting like a dog.   Ground HOG day, experienced health shutdown before many times!!  It’s taken only 2500km to recover, I’m feeling lost better, 85 -90% normal fitness, and another 3 weeks should do it.

      So my advice to try. Crawl out of your sick bed, in summer heat, start riding daily for hours on end – SEE WHAT Happens !! First week will be horrible as the stored toxins from poorly procced food hit the blood stream. I’ve even experienced liver stones passing type pain for first 2-3 weeks.  You will find hard long rides have great impact, results seen next day.  We are all different. My issue has always NOT been the big D but Constipation, massive weight gain, fatly liver from know where. Diet change won’t work for me alone, need  zero impact cardio exercise, Medical studies confirm diet + exercise helps PCS issues. Running I find is bad, just bounces the mass around for more fat to be squeezed in as testified by others! I may have had bile duct injury repaired on the fly, but my doctors / hospitals won’t investigate, they take the far left opinion, post issues don’t exist, it’s in your head , take some antidepressant medication for IBS. After 5-6 GI’s in private consultations over many years looking for a diagnosis one wonders what it’s like to be an ATM machine, very painful with no income what so ever for years. 

      I’ve discovered a lot more through years of reading medical studies. And I think Mediterranean diet works well but you have to live in heat, Mediterranean climates. Happy to share more. There a FB group called GB S ruined my L, I’m a member, touch base I can share more notes to a fellow cyclists – health, fitness and outdoors freak. The very very best Jason    Note: we are all different, male , female, no procedure done the same for all, 4 different types of stones, 20+ different root causes , removing the gallbladder doesn't  always fix problems. but can makes more issues or exciting worse of for the majority , majority  all is good after removal?.  GB must come out if its about to KILL you smile

  • Posted

    Good Morning let me tell y’all what happened to me last year on March 16,2017 I had 3 surgery on my gallbladder bladder that week along and just had a stint removed out my liver in November because of the gallbladder surgery. I couldn’t walk or talk or sit up in the bed by myself I stayed in the hospital a month the story is longer than this I’m just getting to the point, right now as we speak I’m having the worst pain ever I still can’t eat anything it comes right back up. I sleep with a heat pad I’m a mother of 3 grown kids and this surgery was the worst ever. Not only that I’m still under the doctor in it’s been a year. 
  • Posted

    Everyone wanted me to sue because the story is way more complicated than the short version I just posted. 
    • Posted

      I'm really sorry to hear this.  It's awful.  I'm now 5 years into my saga and still need more surgery.  The thing with these operations is that most of the time they go well.  But, and it's a big but, when they go wrong they go wrong big time.  And the NHS just band together and don't take responsibility.  It's dreadful. Keep strong

  • Posted

    I had my gall bladder out on April 21st 2018 and still have persistent symptoms. loose stools, severe bloating, sharp abdominal cramps, discomfort in the liver. Some of these pains feel the same as when the Gall Bladder was still there and some are new. Things have started to improve little by little but the timeline is way off for a "typical recovery" after this procedure.

    The best I have found on the subject is that those of us having issues are one of the unlucky 15% of patients that get something called "Postcholecystectomy Syndrome" or PCS. https://emedicine.medscape.com/article/192761-overview

    It gets us no closer to relief, this needs to be worked out by doctors but you need to find a doctor who will listen and take care in finding the underlying issues. I am just starting to dig into why I do not feel better than I do. I wish everyone luck.

  • Posted

    After 9 month of very very high liver levels, blocked bile duct, and specialists telling me that my gallbladder was certainly going to be coming out I was operated on. That was nearly 2 year ago. I lost a healthy 3 stone, I was feeling marvelous. Now, im feeling uncomfortable again. Burning sensation comes and goes daily. Getting up in a morning feel nauseous. Practically a constant dull ache, and feeling worn down with it. A few week ago, I contracted a stinker of a cold, with a persistent cough lasting over 3 week. Doc last week sent me for a chest xray which came back negative. Because nowadays a doc can only see to one ailment at a time for 10mins, I felt I couldn't raise this issue. I am going to try to see doc next week if appointment's allow. In the meantime do these symtons ring true with anyone, and any advice would be good. I'm taking a pre-prescribed 15mg lansoprazole I found,hoping this might settle the burning, just a couple days in on those pills. I can also state, cold drinks and sometimes just eating can trigger discomfort not long after intake...just like the old days of having a gallbladder.

    • Posted

      My heart goes out to you. Read my reply on how I use oil of oregano. ❤️
  • Posted

    I take oil of oregano for pain in that whole region. Definitely buy it at a health food store and I recommend shaking it up in a covered glass bottle before every sip. Look up on the Internet for frequency & dosages. Too much can cause serious harm. I go off it every so often, but return to it as the pains return. It and taking activated charcoal just a few times totally got rid of duodenum burning that I had for months after my gallbladder was removed from my side. Billiary stent removal upsets the duodenum area, and I had two stents installed back to back after getting pancreatitus. Oil of Oregano helps that, too. It reduces inflammation. Make sure to eat small portions and regularly. I feel ill if I over eat or go too long between meals. Too much fat good types or bad puts a strain on liver. Deep fried foods and too much of any kind of meat are no no’s. Make sure not too lay down until your stomach is empty. Pale stools are fatty stools. Stones and sludge can form in the liver so a proper diet and exercise are essential. Do what you can to keep your liver healthy. A blended drink of lemon water with a handful of parsley and a cucumber will help clear the liver. It’s said to do it once a day for 2 weeks and it cures fatty liver. I’m not a doctor so look all this stuff up and consult yours. Mine was very curious how I got rid of the duodenum burn! Wishing everyone here the best. ...My operation was 18 months ago. 

  • Posted

    Guys do not start taking any addiction medication like opioids, it’s realy bad but you can try duloxetine, and use cannabis oil and use valerian. Combined this is a good use. The pain is the nerve where the gallbladder used to sit, the bed of the gallbladder and this nerve is active still. You can also try nefopam, good luck stay strong and try ice packs with hot water bottle 

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