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TTNOGluten

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TTNOGluten Explorer

Well after a follow up to see the gastro, got some interesting news, I have been gluten free now for over five months, my epigastric discomfort and back/rib pain continue, but after a EGD on tuesday my biopsy is now reported as normal and my labs are also normal. So I guess I am happy, just still trying to figure out why my symptoms seem the same. Curious to know if the musculoskeletal pain, ribs, back, and belly continue even after your intestine looks normal under a microscope?? Any thoughts????


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pondy Contributor

My biopsy came back pretty much "normal" also (yea!) - but like you, my upper left GI pain continued... turns out my stomach was full of H Pylori. I am thinking that was a primary cause for the pain because - happy fo report - that pain has pretty much subsided now that I am about 2 weeks post antibiotic treatment.

So, I don't know if that helps or anything... but also - sugar, soy and dairy can bring the pain right back in my case.

I hope that you discover & eliminate the source(s) of pain soon!! I can empathize with you. So very sorry that you've been suffering!

Hang in there!

Pondy

YoloGx Rookie

I have found eating more home made cultured food (yogurt, sauerkraut) and gluten-free miso to repopulate the gut with good bacteria really helps. It also helps to eat things like adzuki beans and avoid heavy animal fats for a while to give the liver and gall bladder a break. Better to eat fish and shrimp etc., and maybe some skinless chicken, but no other meat--and eat lots of fresh greens and drink lots of water. No doubt right now the liver/gallbladder and kidneys are overworked due to likely leaky gut going on because of the damaged villi in the intestines. This distress then gives one intestinal, back, neck and shoulder pain as well as headaches.

Katrala Contributor

Maybe it isn't gluten-related? Those without celiac disease can also have such problems as well.

Has your doctor looked into any other non-celiac reasons?

TTNOGluten Explorer

I have had so many tests it seems that it is making me confused at times. Most of them continue to come back negative, yet the nausea, back and rib cage pain, and dizziness in the morning continue. Starting to feel helpless with finding an answer as I just want to feel better. Prior to August 9th I felt great and then bam overnight all of m symptoms came on. Never any GI problems before, but now overnight I have celiac disease, also never have I had any dairy problems for 41 years and now bam all of the sudden I allergy test to have a casein allergy?? I do what I am told, and eliminate these things, and no improvement, even had my gallbladder taken out, still nothing. I am beginning to think this is something neurologic, although MRI of brain looks normal. Really at this point I just want my life back from this nonsense. I will keep looking for answers until I come up with one that makes me better. Who knows maybe this is what I am to expect with celiac disease. Maybe even after the villi heal and labs normalize you still have symptoms. People talk of being glutened. I never knew really what that meant, because since the start of this on August 9th, I have never had one day of feeling well to know what getting glutened is?? Who knows?

Thanks for your answers I hope to read others insight, and hope that someone else has felt the way I do that can guide me in the righ direction

burdee Enthusiast

After I was dx'd with celiac disease and casein allergy I went gluten/casein free. Symptoms continued. I soon suspected and stool test later confirmed soy intolerance. 2 years later ELISA tests confirmed 4 more delayed reaction (IgG mediated) food allergies. During the 4 yr period after my celiac disease I was tested for, dx'd with and treated for 8 different gut bug infections (5 bacterial, 2 parasitic, one yeast). Symptoms continued. I found a new ND who looked for why I kept getting symptoms (and infections). Tests showed low stomach acid production, low vit D3, low thyroid (Hashimoto's actually) and low white blood cells. After resolving with supplements and/or treating all that I finally have normal digestion and no more 'gluten' symptoms, which were really caused by a myriad of other things. I still have sensitivity to sorbitol and other alcohol derived sugars, because of leaky gut. The longer you had undiagnosed (or misdiagnosed celiac disease), the more likely you have leaky gut and/or other food alleries and/or autoimmune diseases and/or other complications.

After you eliminate gluten and all sources of cross-contamination, don't just assume your ongoing symptoms are gluten related. Get tested for other things from a holistic doctor who considers other delayed reaction food allergies, gastrointestinal infections, other digestive problems (like low stomach acid production) and other autoimmune disesases. (Hashimoto's causes constipation, which I thought was my celiac/food allergy reaction. Interestingly after I normalized my thyroid function with supplementa, I got diarrhea (instead of constipation) the next time I accidentally ingested one of my allergens. Depending on how long you had undx'd celiac disease, you may need to resolve many issues before you are symptom free. Nevertheless, the journey is well worth feeling healthy finally.

Bubba's Mom Enthusiast

Just another thought..I had been on PPI medication for relux for years. After going gluten-free and soy free, I was still having a burning pain, much like you described. I also have a low functioning gallbladder, and it was recommended I have it taken out.

In my search to find info about biliary dyskenesia, and what *might* help bring my function back to normal, I found a link between PPIs and dysfunction. I asked my new Dr. if he thought my GB function might improve off gluten and maybe off the PPI? He told me to try it and see if it helps.

Since stopping the PPI, my pain is much less. I also don't have the terrible GERD I had before my DX and going gluten-free. Now I'm assuming gluten was causing my reflux, not excess acid?

If you are on a PPI, ask your Dr. if it's safe to try going off it for a bit to see if it helps your pain?

You may also have areas that aren't healed 100%? The endoscope isn't long enough to check your entire small intestine, and if samples were taken from the part it could reach, it's possible there's patchy areas that are still healing? It would be hard for the Dr. to know to grab a sample in one of those areas if the damage isn't obvious to the naked eye? It sounds like you are on the right path to healing though!


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    • marion wheaton
      Thanks for responding. I researched further and Lindt Lindor chocolate balls do contain barely malt powder which contains gluten. I was surprised at all of the conflicting information I found when I checked online.
    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
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