Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Gallbladder Issues And Celiac


Guest BornToRide

Recommended Posts

Guest BornToRide

I started having what I think are gallbladder issues. I have always has some minor pain for years here and there on the right side under the ribcage. Well, it really started acting up recently when I changed my diet (no I do not eat a lot of fat or fried foods - never have). I have since learned that gallbladder disease is often a component of celiac disease, but should get better once the gluten is removed from the diet.

What have you experienced in this respect, if any?


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Mtndog Collaborator

There is some relationship. In fact, myself and jaten had our gall bladders out around the same time last May. I had gall stones that they found while trying to diagnose me with celiac. I waited a year and finally had the surgery. No regrets at all!

DEFINITELY get it checked out because going gluten-free won't get rid of the stones (as far as I know) and you should find out what's going on. They generally will do bloodwork and an ultra-sound to see and then you can go from there.

Guest BornToRide

Yes, I have an ultrasound scheduled next Fridays to check. What kind of supplements do you need to take since you no longer have a gallbladder and does that work well? Also, how did you find that you were legume intollerant too?

Viola 1 Rookie
I started having what I think are gallbladder issues. I have always has some minor pain for years here and there on the right side under the ribcage. Well, it really started acting up recently when I changed my diet (no I do not eat a lot of fat or fried foods - never have). I have since learned that gallbladder disease is often a component of celiac disease, but should get better once the gluten is removed from the diet.

What have you experienced in this respect, if any?

If the pain is on the right side and below the rib cage, it may be gall bladder, but frequently the ultra sound will be just fine and the pain turns out to be the illium.

Because of the Celiac digestive system, quite often particles of food will pass through the intestine a little larger than normal and sit in the illium, which causes irritation. This will show up on the tiniest gluten contamination. There really isn't much that can be done for it except try as hard as possible not to be contaminated. Which of course we all do anyway.

Mtndog Collaborator
If the pain is on the right side and below the rib cage, it may be gall bladder, but frequently the ultra sound will be just fine and the pain turns out to be the illium.

Because of the Celiac digestive system, quite often particles of food will pass through the intestine a little larger than normal and sit in the illium, which causes irritation. This will show up on the tiniest gluten contamination. There really isn't much that can be done for it except try as hard as possible not to be contaminated. Which of course we all do anyway.

Viola- This is really good to know- I had no clue about that!

You don't need to take any supplements if you have your gall bladder removed. It's like a "storage facility" for bile and once it's gone, your liver readjusts (USUALLY rather quickly) and produces less bile. I am DEFINITELY not advocating you have the surgery....that's up to you and your doctor, but telling you this in case you decide to.

I had mine because I am trying to get preggers and they said many women have gall bbladder problems AFTER pregnancy and I didn't want to risk having to have my gall bladder out while pregnant.

As far as the legume intolerance goes, I cut out gluten and replaced it with a lot of soy and peanut butter but still felt icky. I realized I was soy intolerant so I cut it out and when I tried to eat it again, I felt really sick. Same with other legumes. So basically it was an elimination diet.

When I eat peanut butter, I feel glutened :( So sad because I LOVE LOVE LOVE peanut butter.

Jo.R Contributor

Oh, no peanut butter. :o That is also one of my favorites, so sorry.

They took my gall bladder out first. The test showed it was irritated. It wasn't until after I found out that I had Celiac that I found out my gall bladder could get better (I didn't have stones) if I went gluten free. I was a little upset, after my deductible and paying 20% we paid over $2000 for the tests and surgery. On the other hand I'm lucky, I have no bad side effects from having it out. My grandmother couldn't digest onions after having her gall bladder out, and I have a friend who has to watch how much she eats of certain foods.

If you don't have stones, I'd wait and see if going gluten free will help. Having it out could limit what you can eat, when you are already so limited. Also if they don't find stones in your ultrasound they will want you to do another test. I can't remember the name, but they inject you with a chemical and watch your gall bladder. If your medical is like mine, I would ask a lot of questions before doing it. It is expensive. Ask your doctor about putting it on hold and see if the gluten free diet will correct the problem. But go through with the ultrasound, you need to know if you have stones.

Good luck!

NoGluGirl Contributor

Dear BornToRide,

I had my gallbladder removed several years ago when I was 20. I had an ultrasound, HIDA scan, and all that. Nothing showed at tall. I knew it still had to be the trouble though. My intuition is always right. I learned the hard way not to ignore it.

My doc relied to heavily on the tests. He figured it could not possibly be gallbladder disease, because my tests showed nothing. I told him I had done some research online, and found out these tests are only about 33 percent accurate at best. :( That leaves a rather large margin for error.

Finally, when I had pestered him enough, he let me see a surgeon. When I saw the surgeon, he was very thorough. I love that! ;) Anyway, I told him about the Abdominal CT I had done more than three years prior. It had showed a gallstone, and that idiot doctor I had at the time missed it. I found that out when my tech told me when I had the ultrasound the fall before! I was so mad I could not see straight.

To this day, if I see that woman, I very well might rip her head off! :angry: She told me I was crazy pretty much. My parents believed her. So did every other doctor I went to see because of that. No matter who I saw, they were already convinced I was not physically sick. I was forced to go to counseling and take nearly every anti-depressant or anti-anxiety drug on the market.

I even was taken up to IU Med where I had an entire team of doctors working on me. I had an endoscopy, intercolisis, gastric emptying study, even more blood work, and a colonoscopy. This was all for them to tell me I was crazy. Naturally, another anti-depressant was perscribed, which I do not know if I will ever get off of. Of all things, the one doctor heading the group was the head of Gastroenterology and Hepatology!

He should have known that! The gallbladder is part of the hepatobialary system! :blink: So, I switched Primary Care Physicians after returning. Then, fast-forward a couple years, and there I sat in the surgeon's office. He said considering my symptoms, I was a candidate for surgery. I felt it was the right thing to do.

My feeling was right. It turns out, at my ten day post-op check up, my gallbladder was very inflamed and irritated, and nearly ruptured. After a while, I was not feeling any better. All my doctor ended up doing was giving me pills. I could not take it anymore. I then read about Yeast overgrowth.

I asked the local healthfood store clerk about doctors that knew about it.

She recommended the doctor I am with now. She is a holistic physician as well as an MD. She is the one who diagnosed me as Celiac. I used to have reflux so bad, I had to sleep practically sitting straight up. Now, I can even occaisionally skip my second dose of Prilosec OTC. That never would have happened before going gluten free.

An important thing to remember is, once you have your gallbladder removed, you need to be careful about your fat intake. Otherwise, you could develop a stone in your bile duct. Also, you normally will get diarrhea and stomach cramps because you cannot digest fat well anymore. If left untreated, pancreatitis can result. There is no cure for that. :( I met a woman who had gone to the ER 15 times in 2 months, and was misdiagnosed. She was told she was crazy. Well, it turns out the tests did not show anything like mine, and it turned out there was a sandy substance made of bile called sludge in there.

It ate through her gallbladder and into her pancreas. She had a feeding tube in her bellybutton.

She told me she had to be extremely strict with her fat intake, cannot ever have any alcohol, and had kidney and liver problems. She was not much older than I was. The woman told me I was making the right decision to get it removed now.

I apologize for this being so long, but I just wanted you to know how important this is. The link between Celiac and gallbladder problems seems pretty strong.

Sincerely,

NoGluGirl


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Mtndog Collaborator
An important thing to remember is, once you have your gallbladder removed, you need to be careful about your fat intake. Otherwise, you could develop a stone in your bile duct. Also, you normally will get diarrhea and stomach cramps because you cannot digest fat well anymore.

If left untreated, pancreatitis can result. There is no cure for that. :( I met a woman who had gone to the ER 15 times in 2 months, and was misdiagnosed. She was told she was crazy. Well, it turns out the tests did not show anything like mine, and it turned out there was a sandy substance made of bile called sludge in there.

It ate through her gallbladder and into her pancreas. She had a feeding tube in her bellybutton.

She told me she had to be extremely strict with her fat intake, cannot ever have any alcohol, and had kidney and liver problems. She was not much older than I was. The woman told me I was making the right decision to get it removed now. I apologize for this being so long, but I just wanted you to know how important this is. The link between Celiac and gallbladder problems seems pretty strong.

OMG- this is horrible!!!!!!!!! I have a question- did your surgeon tell you that you needed to watch your fat intake after your gall bladder removal? Mine never said anything :unsure:

And the woman you're referring to had this because she DIDN"T have her gall bladder out, right? :ph34r:

NoGluGirl Contributor
OMG- this is horrible!!!!!!!!! I have a question- did your surgeon tell you that you needed to watch your fat intake after your gall bladder removal? Mine never said anything :unsure:

And the woman you're referring to had this because she DIDN"T have her gall bladder out, right? :ph34r:

Dear Mtndog,

Yeah, this poor woman. I felt so sad for her. She, like many of us, are left dealing with permanent mistakes doctors made. :( My surgeon did not tell me to watch my fat intake, but I was talking to someone else in the waiting room that said she had diarrhea the first six months after her operation. I came across this while doing research on the internet. I later asked my primary care physician, and he said that it is a good idea to be careful. If I eat too much fat, I get cramping, diarrhea, and nausea. My reflux usually increases as well.

It is just according to the research I have done, you can still get stones in your bile duct. Watching your fat intake after the surgery can prevent this. Fat in excess is bad when your body no longer has the organ that processes it. A blockage in the bile duct can cause bile to back-up in your system, leading to pancreatitis, and liver damage.

The woman I told you about developed those problems because by the time they did take out her gallbladder, damage was done. They waited too long. She tried to tell the doctors, but naturally they wrote her off as a mental case. :( Now she is left suffering damage that cannot be reversed.

Sincerely,

NoGluGirl

Mtndog Collaborator
Dear Mtndog,

Yeah, this poor woman. I felt so sad for her. She, like many of us, are left dealing with permanent mistakes doctors made. :( My surgeon did not tell me to watch my fat intake, but I was talking to someone else in the waiting room that said she had diarrhea the first six months after her operation. I came across this while doing research on the internet. I later asked my primary care physician, and he said that it is a good idea to be careful. If I eat too much fat, I get cramping, diarrhea, and nausea. My reflux usually increases as well.

It is just according to the research I have done, you can still get stones in your bile duct. Watching your fat intake after the surgery can prevent this. Fat in excess is bad when your body no longer has the organ that processes it. A blockage in the bile duct can cause bile to back-up in your system, leading to pancreatitis, and liver damage.

The woman I told you about developed those problems because by the time they did take out her gallbladder, damage was done. They waited too long. She tried to tell the doctors, but naturally they wrote her off as a mental case. :( Now she is left suffering damage that cannot be reversed.Sincerely, NoGluGirl

I feel so bad for that poor woman.

I knew that you could get stones in your bile duct but I didn't know that watching your fat intake could help with this. Good to know as I have been suffering bouts of nausea and diarrhea that my doctor kept telling me was a virus (a 6 week virus? C'mon!). I see my GI next week and will mention this to her. maybe it plays into what's happening with me.

Thank you for the info!

NoGluGirl Contributor
I feel so bad for that poor woman.

I knew that you could get stones in your bile duct but I didn't know that watching your fat intake could help with this. Good to know as I have been suffering bouts of nausea and diarrhea that my doctor kept telling me was a virus (a 6 week virus? C'mon!). I see my GI next week and will mention this to her. maybe it plays into what's happening with me.

Thank you for the info!

Dear Mtndog,

You are so welcome for the info! It is scary, isn't it? I have been having pain under my ribcage again, and I am concerned this could be my trouble as well. The symptoms are pretty much the same as gallbladder disease. It has been difficult to find low-fat gluten-free food. I think that is the trouble. Too much fat is problematic. I know there are instances where there is damage done to the common bile duct, the papilla of Vater, and the Sphincter of Oddi. This is not common though. If that was the case, you probably would have suffered trouble right after surgery. Doctors can be so goofy. A six week virus. Right. :rolleyes: That is like saying to a woman who is 7 months pregnant she is sort of expecting! :lol: Your GI may be able to help you.

I really wish I could have done something for that poor woman, too. It is so unfair what happened to her. What is worse is, doctors have all the good attorneys, so when they screw up, they win anyway! They could kills someone in cold blood and get off. It makes me furious! :angry: My mother's best friend's mother-in-law bled to death because of a nurse's major mistake. She was there having dialysis that she needed due to the effects of her Diabetes. The nurse did not pay attention, and while attempting to put the IV in, hit a jugular (major artery) in the back of her neck. Blood was running all down her neck when they came in later. By that point, she had lost so much blood, it was too late. She bled to death. :( They tried to take them to court, but couldn't afford to. Other attorneys were already on retainer for the hospital, and could not do it. They would have had to go out of town to get someone who could represent them.

Sincerely,

NoGluGirl

tabdegner Apprentice

I just have to add to the whole gallbladder issue. I had mine out in January 2004 after 3 months of HORRIBLE pain. The dr couldn't figure out what was wrong because an ultrasound didn't show gallstones and I didn't have "classic" symptoms. After landing in the ER the day after Christmas, they finally did a HIDA scan and it showed my gallbladder wasn't functioning. When they took it out it was very very inflammed and "mangled" up as they said.

I was completely FINE and a new person for about 6 months after that and then the trouble started. I all of a sudden couldn't digest fat again. After many tests from the GI doctor, including an endoscopy and biopsy for celiac, he basically told me that I had postcholysisectomic syndrome. Which is trouble digesting fat even if you have your gallbladder out. He thinks my duct was still spasming when it was realeasing bile, or something like that. And he also said that they couldn't find anything wrong with me.

I was able to control symptoms with some meds for a few months, but now I am having horrible problems again and it's more than digesting fat, it's digesting anything, period. Just went to the GI doctor again last week and he said I have IBS, maybe gasteroparisis, and gave me more meds. YUCK. And again he said that he has no idea what's wrong with me.

I am going gluten free for at least 2 weeks to see if that helps. My dr. said I don't have celiac, but with my strong family history (see my signature below) and every symptom in the book (almost) I don't see how I can NOT have celiac.

I think that either the gallbladder triggered celiac or the celiac triggered the gallbladder problem. Either way, I think they are very connected. And I am SO DONE WITH MEDS AND DONE BEING SICK!!! Wish me luck in my gluten free adventure!!!

Mtndog Collaborator

Tabdegner- Welcome to gluten-FREEDOM!!!!!!!!!!!!!!!!!!!!

Guest BornToRide

Thanks everyone for your inputs. I am sorry for the suffering some have endured. I just don't get it - the oath says do no harm. Not doing the right thing or anything does harm too :angry:

AZKat Newbie
Dear Mtndog,

You are so welcome for the info! It is scary, isn't it? I have been having pain under my ribcage again, and I am concerned this could be my trouble as well. The symptoms are pretty much the same as gallbladder disease. It has been difficult to find low-fat gluten-free food. I think that is the trouble. Too much fat is problematic. I know there are instances where there is damage done to the common bile duct, the papilla of Vater, and the Sphincter of Oddi. This is not common though. If that was the case, you probably would have suffered trouble right after surgery. Doctors can be so goofy. A six week virus. Right. :rolleyes: That is like saying to a woman who is 7 months pregnant she is sort of expecting! :lol: Your GI may be able to help you.

I really wish I could have done something for that poor woman, too. It is so unfair what happened to her. What is worse is, doctors have all the good attorneys, so when they screw up, they win anyway! They could kills someone in cold blood and get off. It makes me furious! :angry: My mother's best friend's mother-in-law bled to death because of a nurse's major mistake. She was there having dialysis that she needed due to the effects of her Diabetes. The nurse did not pay attention, and while attempting to put the IV in, hit a jugular (major artery) in the back of her neck. Blood was running all down her neck when they came in later. By that point, she had lost so much blood, it was too late. She bled to death. :( They tried to take them to court, but couldn't afford to. Other attorneys were already on retainer for the hospital, and could not do it. They would have had to go out of town to get someone who could represent them.

Sincerely,

NoGluGirl

I wanted to share what sometimes helps me with the pain under the ribcage. I also had my gallbladder out several years ago, it was not working, no stones but report after surgery said chronic inflammation and infection. When I have that pain, or indigestion even, I eat about 1/2-3/4 cup of organic UNsweetened applesauce. There is something about the malic acid in apples and applesauce that helps loosen up the bile. While it doesn't completely clear it up every time it almost always reduces the pain to at least a bearable level. Hope this will help you and others with this problem.

Mtndog Collaborator
I wanted to share what sometimes helps me with the pain under the ribcage. I also had my gallbladder out several years ago, it was not working, no stones but report after surgery said chronic inflammation and infection. When I have that pain, or indigestion even, I eat about 1/2-3/4 cup of organic UNsweetened applesauce. There is something about the malic acid in apples and applesauce that helps loosen up the bile. While it doesn't completely clear it up every time it almost always reduces the pain to at least a bearable level. Hope this will help you and others with this problem.

It's funny that you say that as I've always said that apples and potatoes are the two best foods for calming my stomach down!

NoGluGirl Contributor

Dear tabdegner,

Good luck with the gluten-free diet! I think it could help. The gallbladder issue is a major problem. There are many possibilities. However, the good thing is, this does not do you any harm. I would be more than happy to send you a list of safe foods. You will be surprised by what we can have, I think. Gallbladder issues were a problem for me probably for several years before it was finally removed. Thank God for intuition, or I would have been so screwed. Do not rely too heavily on your doctor. A lot of people have difficulty in readjusting after the operation. Your body cannot digest fat well most of the time. At least the postcholecystomic syndrome could be a possible answer to my troubles.

Dear AZKat,

Thank you for the tip. I will have to try that! Someone else on here was talking about how Celiac irritates the illium (a part of the body) that is located near there. I found that interesting. It is frustrating dealing with this misery on a daily basis. You think it was all going to be okay after the surgery, and yet you still suffer. :(

Sincerely,

NoGluGirl

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,548
    • Most Online (within 30 mins)
      7,748

    Lunaluv
    Newest Member
    Lunaluv
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.