Post-cholecystectomy or gallbladder removal surgery
Hi – I had my gallbladder removed 17 years ago and have chronic, sharp back pain behind the port incision. That incision was in my upper left abdominal quadrant; the pain is felt in my back, directly behind the incision. It is thought that I have an adhesion in my upper left quadrant. Is it possible that nerves are trapped and that it causes referred pain in my back? The pain is nauseating and hasn't improved. I have been on anti seizure medication and a pain killer that isn't a percocet-type medication. I am curious if anyone else has persistent pain in their back following gallbladder surgery. If so, how is your pain treated.
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OH NO!! Scopolamine patches will constipate you.. they sent me to the hospital constipated..and the first thing the ER doctor said.. patches.. constipation..don't wanna scare you!! (I had my gallbladder out not emergency.. but "rushed")... Please ask your doctor about that patch.. I use Zofran and Promethazine for nausea..and Trulance (AM) and MiraLAX ( at night) and VSL3 Probiotics to help with constipation. And watch what I eat.. been constipated all my life.. also you can try Smooth Move tea..(didn't work for me but did for my sister and niece.. who only went once a month) I drink 2 Vanilla plant based Ensures.. plant protein 5 grams of fiber and 50% Vit C and D.. so with 2 you get 100% and eat Thomas multigrain English muffins with Country Crock plant butter 1 a day ..8 grams of fiber.. if you can do wheat..I hope this helps you!! Please ask about that patch!! Other alternatives to nausea..I'll be praying for you!!
I underwent emergency gallbladder removal surgery about 8 weeks ago. Now I am wrestling with near daily nausea, acute constipation, and occasional vomiting, I’m afraid to eat much, don’t have any appetite anyway, and am curious to know what has helped anyone else in a similar path? I’m wearing scopolamine patches round the clock, and taking laxatives to move my bowels. But this is really a tough recovery process, I can tell you!!
My sister had the same thing after her gallbladder surgery. She lived on Imodium until a doc put her on amitriptyline. It made a big difference. With the Imodium she remained in fear of having an accident while not at home before the Imodium took effect. The amitriptyline seems to work all day.
Thank you . I will check out Dr B Ardis’s podcast.
I just had another thought about this medication. Is this the one that's related to Ozempic, that was renamed. I would strongly encourage everyone to delve into Dr. Bryan Ardis's podcasts and see what he has to say about these meds!
Thank you for responding! Yes! I actually didnt have an endoscopy/colonoscopy up until last month. 😬 I was scheduled to set up an appointment last year in May but when my HIDA scan results came back, they scheduled me for surgery instead. I found out just yesterday that after surgery i was supposed to have an ultrasound and everything rechecked if the symptoms didnt go away, so its on the list now im waiting to hear back on the date for that. But YES even after surgery i still have the same symptoms i just dont have the boot feeling under my right rib cage anymore, shes had me on a low fat diet, high fiber diet, and a few others. I can eat the same thing breakfast, lunch & dinner all week…. Each day is different sometimes id be running to the bathroom in the middle of trying to eat, sometimes i go days without, it varies day to day. Minute to minute it feels like. I actually never gotten the COVID vaccines. Ive taken numerous medications, she started treating it as acid reflux but we trial and error (i would have to look at everything weve tried) its been so long, my brain isnt what it used to be anymore😅 now im on a trial of IBSRELA, today was my first day.
You’re welcome. Good luck! I hope you can keep it.
@blessedwildapplegirl
Thank you❣️❣️❣️
Based on your story and experience (thank you for sharing), I will try to keep my low functioning gallbladder as long as possible. 😉
Unless your gallbladder is filled with stones that they can’t get rid of, or is actually dead, don’t let them take it out! Oh, my God, I almost died after they took mine out because I couldn’t digest anything. I weighed 73 pounds for five years and subsisted on mashed potatoes and canned carrots. I’m 5 foot four. I’m finally back to being able to eat, although I’ve had something going on since last November, but before that I was eating, but I cannot longer eat any raw vegetables, no spices of any kind, so no prepared foods, fat doesn’t go down, (except for avocados and for a while, coconut milk yogurt, but then that started making me sick), the list goes on. Without a gallbladder, you don’t have enough digestive acids to fully digest your food and then you don’t absorb your vitamins, etc. It’s really dangerous and they shouldn’t even do it. They should check our gallbladders periodically and make sure they don’t have stones so they don’t have to take them out ever. It basically killed my mom because after they took hers out, she had constant diarrhea and began kind of wasting away and then she had such terrible acid reflux that they put her on a proton pump, inhibitor, which broke both of her hips, and also she got two infections, C diff and E. coli, which I have read is not that uncommon if you don’t have enough stomach acid. Her body couldn’t fight them. I would give anything to have my gallbladder back. I told the doctors for six years before it went out that it was going out and because they’re Pipida scan said that it wasn’t they didn’t believe me. I was right, but by the time they found it, it was already dead, and I had to remove it, or I would’ve gotten sepsis. I’m scheduled to have a colonoscopy in a couple of weeks and honestly, I don’t even trust doctors. Not sure what to do. I guess I’ll go, but I haven’t had very good experiences with doctors. It seems so difficult to find a really good one. Good luck to you, but again, I would keep your gallbladder if you can, unless it’s actually dying. 💕
Hi @bunnycuddlez , and welcome to Connect!
You are going through some awfulness, I am sorry. My journey includes some of what you describe and I so wish I could give you an easy button to push. I can say, keep moving forward. Joining Connect is a great step to take.
There certainly is a lot going on in our guts, and it sounds like you are in a good place with a GI that is making sure your anatomy, all your parts are working the way they should. That will be another step forward. You have some great input from others, too. It may move you forward even quicker to focus on what you can control in the meantime. Regular exercise and good, consistent meals helped me figure out they play a role. I have a regular routine so when it changes I can point to it. One example, I knew when I felt absolutely horrible after changing my eating routine and fasting for 10am blood work recently that going too long without eating makes a difference for me. Information like that is what only I can identify and helpful for my doctor to know.
Do you eat any differently since getting your gall bladder out? When do you have your CT and stomach emptying tests?