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

Severe Pain, Celiac Issue


LouiseF

Recommended Posts

LouiseF Newbie

Hello,

My GI Dr suggested I come here and look for some help because he is at the end of testing and doesn't know what else to do.

I was diagnosed with celiac disease 5 full years ago. Have been diligent about staying away from gluten. Each year I get my celiac disease tested and my numbers are always well below 10.

I had intestinal pain before this for 25 years. After getting off of gluten it never went away. Last October a new severe pain started in my gall bladder area. I have had an ultrasound, Hida scan, CT scan and colonoscopy. All test results came back that everything was fine. I had an endoscopy with a test and it showed that my villa spore was still damaged. To my dr that indicated I am still being exposed to gluten. I don't see how.

The pain now (4 months later) can be very bad in my gall bladder. He thought it was biliary dyskinesia and wants to take the gall bladder out. I would rather not.

He is sending me to a nutritionist next monday in the hopes that he can help me.

Anyone have any ideas of what this pain could be from?

I have a VERY healthy diet and in the past year I have lost 52 lbs.

I would appreciate any suggestions from anyone.

Thank you


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



Celiac.com Sponsor (A8-M):



LouiseF Newbie

I did a post earlier stating that had intestinal pain for 25 years. I forgot to mention something important.

5 full years ago I found out that I have celiac disease.

I have been real strict about staying off of gluten ( as far as I know).

My intestinal pain never went away.

Last October I started with a new real bad pain in my gall bladder area.

Since then I have had ultrasound, Hida Scan, Ct Scan, colonoscopy. All test results came back negative.

I had bloodwork showing IgA deficient. Now my GI dr is perplexed and suggested I come here and see if someone can help me.

Endoscopy showed villa sprue damage as if I was still getting gluten. I don't see how.

I am trying to eat only warm foods, no food combinations that will promote fermenting of foods in my belly.

I take 30 billion pro-biotics. It all isn't making it go away. This pain has been here for 4 months now.

Any suggestions would be greatly appreciated.

burdee Enthusiast

I did a post earlier stating that had intestinal pain for 25 years. I forgot to mention something important.

5 full years ago I found out that I have celiac disease.

I have been real strict about staying off of gluten ( as far as I know).

My intestinal pain never went away.

Last October I started with a new real bad pain in my gall bladder area.

Since then I have had ultrasound, Hida Scan, Ct Scan, colonoscopy. All test results came back negative.

I had bloodwork showing IgA deficient. Now my GI dr is perplexed and suggested I come here and see if someone can help me.

Endoscopy showed villa sprue damage as if I was still getting gluten. I don't see how.

I am trying to eat only warm foods, no food combinations that will promote fermenting of foods in my belly.

I take 30 billion pro-biotics. It all isn't making it go away. This pain has been here for 4 months now.

Any suggestions would be greatly appreciated.

After I was diagnosed with celiac disease and casein allergy, I abstained from those and also had continual gut pain. Later tests diagnosed 5 more delayed reaction (IgG and IgA) food allergies. Abstaining from those foods helped somewhat. However, continual gut pain influenced me to request tests for gut bacteria, parasites and yeasts. Over a 4 year period I was diagnosed with and treated for infections from 5 different gut bacteria, 2 parasites, and one fungus. Nevertheless some digestive pain continued until another doctor tested my stomach acid production and diagnosed low stomach acid which prevented me from completely digesting what I ate and caused bloating, gas and cramping pain. Now I can finally eat and digest normally with digestive supplements and abstinence from all my food allergens. I also continued to abstain from any kind of alcohol derived artificial sweetners, which can cause similar symptoms.

So I suggest you get a blood test (ELISA) for other delayed reaction food allergies, a stool test for gut bugs and a stomach acid production test to see if your digestion is impaired. (Good luck with that last one, because most docs are brainwashed by Big Pharma's acid blocker drug campaigns.)

LouiseF Newbie

After I was diagnosed with celiac disease and casein allergy, I abstained from those and also had continual gut pain. Later tests diagnosed 5 more delayed reaction (IgG and IgA) food allergies. Abstaining from those foods helped somewhat. However, continual gut pain influenced me to request tests for gut bacteria, parasites and yeasts. Over a 4 year period I was diagnosed with and treated for infections from 5 different gut bacteria, 2 parasites, and one fungus. Nevertheless some digestive pain continued until another doctor tested my stomach acid production and diagnosed low stomach acid which prevented me from completely digesting what I ate and caused bloating, gas and cramping pain. Now I can finally eat and digest normally with digestive supplements and abstinence from all my food allergens. I also continued to abstain from any kind of alcohol derived artificial sweetners, which can cause similar symptoms.

So I suggest you get a blood test (ELISA) for other delayed reaction food allergies, a stool test for gut bugs and a stomach acid production test to see if your digestion is impaired. (Good luck with that last one, because most docs are brainwashed by Big Pharma's acid blocker drug campaigns.)

Thank you for the nice response. My GI Dr said that he doesn't believe in food allergy testing ( because I asked him to do some). he felt they can be inaccurate.

I was tested for parasites by a naturopathic dr and my gi dr gave me an antibiotic about 6 months later just incase. So it is hard for me to stay away from definitive foods but I don't consume much sugar, dairy or meat. I have some but not much. After reading peoples posts it almost seems like I need to stay off of them 100% as a test.

I also took an acid reducer for a month through the GI dr as an experiment. No results. I am very much into herbs and natural health so I can discuss this new issue about acid with my naturopathic dr and see if there is something that she recommends.

I am so far from Big Pharma, I stay away from them. that is all the dr know. It is VERY sad. thanks again.

ravenwoodglass Mentor

You say you stay away from meat. Do you consume soy? It may not be the case for you but soy gives me the pain you describe. It took me 5 years to figure it out. Are you eating mostly fresh unprocessed foods? Are you being careful about CC in your home and especially in restaurants? A very few of us are sensitive to distilled gluten in alcohol. Are you someone who drinks distilled gluten beverages? If yes then try switching to something for sure gluten free like wine and see if that helps.

Simona19 Collaborator

I would like to suggest something too. Can you be fructose intolerant? I'm and after going gluten free I will have a very bad and strong reaction to fructose now. Before I had bloating, gas, occasional diarrhea from it, but now I will have excruciating pain in my intestines. It feels like somebody chop me in half. I must stay away from things that have high content of fructose - apples, pears, syrup, jelly, fruit from jars, etc. If you eat mostly vegetable and fruit, can this be your problem?How to find out, if you are fructose intolerant is to have hydrogen breathing test, or eat 1-2 apples on empty stomach and wait 3 hours. If you will react with pain, bloating, then you are fructose intolerant. Try to avoid fruit with high content of fructose. Berries and small amount of citrus fruit is ok to eat.

Also I'm also reacting to other vegetables like broccoli, cauliflower, cabbage, Brussels sprouts, etc. It happened after gluten and casein free diet. I will have them in very small amounts and I will have strong reaction anyway. Before I had bloating, now pain.

Because I mentioned breathing test I would like to tell you about SIBO. It can also cause pain in the intestines. My doctor gave me also antibiotics to kill it, but after about two months I still had pain and bloating. I asked the doctor to check it again, if everything was killed-bacteria the first time. I had another test and it was positive. I got second round of stronger antibiotics.

Did you have CT with contrast? Did doctor checked, if you don't have any obstruction that can cause pain?

Also one last thing. Can you have pinched nerve in your spine that is causing problems in your right upper quadrant? It's the long shot, but when I went to a chiropractor, I saw a poster in his office where was spine and nerve connection to each organ. I mentioned this just in case.

I hope that you will find very soon what is causing this pain and have pain free life again.

Bubba's Mom Enthusiast

I did a post earlier stating that had intestinal pain for 25 years. I forgot to mention something important.

5 full years ago I found out that I have celiac disease.

I have been real strict about staying off of gluten ( as far as I know).

My intestinal pain never went away.

Last October I started with a new real bad pain in my gall bladder area.

Since then I have had ultrasound, Hida Scan, Ct Scan, colonoscopy. All test results came back negative.

I had bloodwork showing IgA deficient. Now my GI dr is perplexed and suggested I come here and see if someone can help me.

Endoscopy showed villa sprue damage as if I was still getting gluten. I don't see how.

I am trying to eat only warm foods, no food combinations that will promote fermenting of foods in my belly.

I take 30 billion pro-biotics. It all isn't making it go away. This pain has been here for 4 months now.

Any suggestions would be greatly appreciated.

My first thoughts are that you have another food intolerance. Your Dr. is right..testing isn't good at finding them. Soy gives me pain like you described and it's in SO many things! I found it hiding in my supplements. It was in my fish oil, D3, in my Multi. It's in salad dressings, chocolate, It's in all sorts of things.

Do you eat a mainly whole foods diet, or do you eat the gluten-free replacement foods? Some peole react to the small amount of gluten those foods contain.

Another thing it *could* be is fructose malabsorption.

It would be a good idea to have the acid level in your stomach tested too.

I was put on acid blocking meds years ago for reflux. Nobody tested my acid levels. Low acid can cause indigestion and reflux, much like too much acid can.

I've been having the very same pain you descibe. My gallbladder function is at 30% and I was told to consult a surgeon about having it removed. I did a bit of looking online and found that biliary dyskenisia can cause those symptoms. I also found that the acid reducer I've been on for years contributes to the dyskenesia. I went off it to see if I get any improvement, because I don't want surgery!

Start keeping a log of what you eat. Note any symptoms you get. Many food intolerances have a delayed reaction, so having everything written down can help you put the pieces of the puzzle together. It took me a while to figure out that soy was "getting me".

Good luck to you. I hope you can get this sorted out.


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



Celiac.com Sponsor (A8-M):



Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - knitty kitty replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      results from 13 day gluten challenge - does this mean I can't have celiac?

    2. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      49

      My journey is it gluten or fiber?

    3. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      results from 13 day gluten challenge - does this mean I can't have celiac?

    4. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      results from 13 day gluten challenge - does this mean I can't have celiac?

    5. - xxnonamexx replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      49

      My journey is it gluten or fiber?

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,368
    • Most Online (within 30 mins)
      7,748

    Klairep
    Newest Member
    Klairep
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • knitty kitty
      @catnapt,  Wheat germ contains high amounts of lectins which are really hard to digest and can be irritating to the digestive tract.  They can stimulate IgG antibody production as your blood test shows.   Even beans have lectins.  You've simply eaten too many lectins and irritated your digestive tract.   You may want to allow your digestive tract to rest for a week, then start on gluten in "normal" food, not in concentrated vital wheat gluten. This explains it well: Lectins, agglutinins, and their roles in autoimmune reactivities https://pubmed.ncbi.nlm.nih.gov/25599185/
    • knitty kitty
      I take Now B-1 (100 mg) Thiamine Hydrochloride, and Amazing Formulas L-Tryptophan (1000 mg).   Both are gluten free and free of other allergens.  I've taken them for a long time and haven't had a problem with them. I take Vitamin A from BioTech called "A-25".  It's gluten and allergen free and made in the USA.  It's a powder form of Vitamin A.  I was having trouble digesting fats at one point, but found I tolerated the powder form much better and have stuck with it since.   Tryptophan and Vitamin A help heal the intestines as well as improves skin health.  I get Dermatitis Herpetiformis and eczema flairs when my stomach is upset.  So I'm healing the outside as well as the inside.   I take one 1000 mg Tryptophan before bedtime.   With the Thiamine HCl, take 100 mg to start.  If you don't notice anything, three hours later take another. You can keep increasing your dose in this manner until you do notice improvement.  Remember not to take it in the evening so it won't keep you too energized to sleep. When I first started Thiamine HCl, taking 500 mg to 1000 mg to start was recommended.  If you've been thiamine insufficient for a while, you do notice a big difference.  It's like the start of a NASCAR race: Zoom, Zoom, turn it up!   This scared or made some people uncomfortable, but it's just your body beginning to function properly, like putting new spark plugs in your engine.  I took 1000 mg all at once without food.  It kicked in beautifully, but I got a tummy ache, so take with food.  I added in Thiamine TTFD and Benfotiamine weeks later and felt like I was Formula One racing.  So cool.  You may feel worse for a couple days as your body adjusts to having sufficient thiamine.  Feels sort of like you haven't cranked your engine for a while and it backfires and sputters, but it will settle down and start purring soon enough.  Adjust your dose to what feels right for you, increasing your dose as long as you feel improvement.  You can reach a plateau, so stay there for several days, then try bumping it up again.  If no more improvements happen, you can stay at the plateau amount and experiment with increasing your Thiamine TTFD.  It's like being your own lab rat.  LoL Yes, take one Benfotiamine at breakfast and one at lunch.  Take the B Complex at breakfast. Take the TTFD at breakfast and lunch as well.  I like to take the vitamins at the beginning of meals and the NeuroMag at the end of meals.   You may want to add in some zinc.  I take Thorne Zinc 30 mg at breakfast at the beginning of the meal.   Are you getting sufficient Omega Threes?  Our brains are made up mostly of fat.  Flaxseed oil supplements, sunflower seed oil supplements (or eat the seeds themselves) can improve that.  Cooking with extra virgin olive oil, avocado oil, or coconut oil is also helpful.   @Wheatwacked likes phosphotidyl choline supplements for his Omega Threes.  He's also had dramatic health improvement by supplementing thiamine.  You're doing great!  Thank you for sharing your journey with us.  This path will smooth out.  Keep going!  
    • catnapt
      good luck! vital wheat gluten made me violently ill. I will touch the stuff ever again.  
    • catnapt
      I wouldn't consider this lucky. I can NOT tolerate the symptoms. And I googled it and I was not even getting 10 grams of gluten per day and I was extremely ill. They'd have to put me in the hospital. I'm not kidding.   I will have my first appt with a GI dr on March 4th   I will not eat gluten again - at least not on purpose   they are going to have to come up with a test that doesn't require it. 
    • xxnonamexx
      What Thiamine Hydrochloride brand do you take? Is it like the other vitamins I have added? What brand Tryptophan and amount do you take. Thanks
×
×
  • 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.