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Indigestion/Gastritis Not Improving


jasonD2

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jasonD2 Experienced

My recent endoscopy showed mild duodenitis. I was taking supplements for candida back in September and they started to cause indigstion, so i stopped. well it never went away and now im finding it impossible to eat. i am drinking chamomile, slippery elm and marshmallow root tea and taking licorice lozenges before meals and its still not improving. some days are better than others but its just not going away. ive been eating less and am loosing even more weight now. i should be at 155 lbs and am at 140. is there anything that can be done to fix this? I can't live like this..im turning into skin and bones.


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lynnelise Apprentice

When I was diagnosed with gastritis and duodenitis the doctor gave me a Rx for Carafate. After a couple of weeks I was able to eat pain free!

ravenwoodglass Mentor

I would suggest dropping all the 'remedies' you are taking. Then after a few days add them back one at a time. Have you tried Pepto Bismal or has your GI reccommended anything? If you haven't mentioned this to the doctor who did the endo you should do so.

jasonD2 Experienced

Did it cure it or just relieve the symptoms?

ravenwoodglass Mentor

Did it cure it or just relieve the symptoms?

For me the pepto cured the problem, I only needed to take it for about a week or two. I took it at the slightest hint of pain after the first time I took it, right after the endo. The only times I have taken it since is the few times I have been glutened or soyed.

  • 2 weeks later...
Tom Riggins Newbie

I had duodenitis. Twenty years ago a doctor prescribed Carafate for me. Great stuff and basically inert but when I've asked other doctors over the years to prescribe it they have acted like it was the last thing they would have thought of. I took it about ten minutes before meals.

  • 3 weeks later...
Chrisco Apprentice

My recent endoscopy showed mild duodenitis. I was taking supplements for candida back in September and they started to cause indigstion, so i stopped. well it never went away and now im finding it impossible to eat. i am drinking chamomile, slippery elm and marshmallow root tea and taking licorice lozenges before meals and its still not improving. some days are better than others but its just not going away. ive been eating less and am loosing even more weight now. i should be at 155 lbs and am at 140. is there anything that can be done to fix this? I can't live like this..im turning into skin and bones.

I have chronic gastritis and was given carafate however I didn't take it cause it was liquid form and I have trouble with taking liquid medicines. My doctor gave me phenergan for the nausea that was caused from the gastritis. This helps me eat. Usually after an hour after taking it I feel tons better and am able to eat and keep the food down.


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  • 1 year later...
amypie Newbie

I was sent to this forum after a google search about mild duodenitis. I had an endoscopy done 2 days ago and my discharge paperwork said I had hiatial hernia, gastritis and duodenitis. I went in for biopsy's on my stomach and intestine to look for an ulcer and check for celiac disease along with bacteria I may have. I was reading JasonD2's posts and it seems we have a few similiar problems. I have not been taking any of the supplements that were montioned here but I was told a year and a half ago I had lactose intolerence and I've been having problems with bloating, nausea, and a huge protruding stomach. I was diagnosed at 17 with IBS and at 23 with diverticulosis. I've also been diagnosed with depression. It seems like these "misdiagnosis'" come with a gluten/celiac intolerence. I was just wondering anyone's thoughts on this. I have been tested but won't get results for 2 weeks. I cut wheat and gluten out for a wwek, accidently had some and got sick. That happened twice. Then I read that it was important to not stop eating gluten before you are diagnosed because it can mees up the test results. I added it back in and didn't have as many problems. From what I read, if I did have Celiac I would be losing weight and I have been gaining and my stomach inflammation is not going away. Any thoughts???

mushroom Proficient

Hi amypie, and welcome.

There are so many myths that circulate about celiac disease, and one of these myths is that if you have not been losing weight you cannot be celiac. There are just as many overweight celiacs who cannot lose as underweight celiacs who cannot gain. I was one of the former, my sister one of the latter. We come in all shapes and sizes. :D

Well, no doubt if you have been reading you will have read about the bloating, nausea and distended abdomen. These are not urban myths. These are for real, although not for all. That is the confusing part about diagnosing celiac - there is such a range of symptoms, and if your symptoms don't fall within the particular doctor's experience he will say you can't have it. But you CAN. And while you are still eating gluten you would not expect your stomach inflammation to go away.

Lactose intolerance is one of the first signs because gluten destroys the part of the small intestine that produces the enzyme to digest lactose. IBS is not a diagnosis in and of itself - it is merely a description of a set of symptoms that doctors cannot pin a diagnosis on. Diverticulosis is a real condition which often accompanies other gastrrointestinal disorders from what I understand. Depression is a biggie - it is one of the main symptoms of the neurological form of gluten intolerance and so many have been on so many anti-depression meds before they are diagnosed.

If I were you I would expect my results to be positive. But even if you are not celiac, you have all the symptoms of gluten intolerance and should go on the gluten free diet anyway. If your doctor is not planning on doing any blood testing, you can start right now. Or you can wait and ask him to perform the celiac panel. Either way, I think you are a member of our exclusive little club :D Come on in!

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    • trents
      So, essentially all of the nutrition in the food we eat is absorbed through the villous lining of the small bowel. This is the section of the intestinal track that is damaged by celiac disease. This villous lining is composed of billions of finger-like projections that create a huge amount of surface area for absorbing nutrients. For the celiac person, when gluten is consumed, it triggers an autoimmune reaction in this area which, of course, generates inflammation. The antibodies connected with this inflammation is what the celiac blood tests are designed to detect but this inflammation, over time, wears down the finger-like projections of the villous lining. Of course, when this proceeds for an extended period of time, greatly reduces the absorption efficiency of the villous lining and often results in many and various nutrient deficiency-related health issues. Classic examples would be osteoporosis and iron deficiency. But there are many more. Low D3 levels is a well-known celiac-caused nutritional deficiency. So is low B12. All the B vitamins in fact. Magnesium, zinc, etc.  Celiac disease can also cause liver inflammation. You mention elevated ALP levels. Elevated liver enzymes over a period of 13 years was what led to my celiac diagnosis. Within three months of going gluten free my liver enzymes normalized. I had elevated AST and ALT. The development of sensitivities to other food proteins is very common in the celiac population. Most common cross reactive foods are dairy and oats but eggs, soy and corn are also relatively common offenders. Lactose intolerance is also common in the celiac population because of damage to the SB lining.  Eggs when they are scrambled or fried give me a gut ache. But when I poach them, they do not. The steam and heat of poaching causes a hydrolysis process that alters the protein in the egg. They don't bother me in baked goods either so I assume the same process is at work. I bought a plastic poacher on Amazon to make poaching very easy. All this to say that many of the issues you describe could be caused by celiac disease. 
    • catnapt
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    • trents
      Welcome, @catnapt! The most recent guidelines are the daily consumption of a minimum of 10g of gluten (about the amount found in 4-6 slices of wheat bread) for a minimum of two weeks. But if possible stretching that out even more would enhance the chances of getting valid test results. These guidelines are for those who have been eating gluten free for a significant amount of time. It's called the "gluten challenge".  Yes, you can develop celiac disease at any stage of life. There is a genetic component but also a stress trigger that is needed to activate the celiac genes. About 30-40% of the general population possesses the genetic potential to develop celiac disease but only about 1% of the general population actually develop celiac disease. For most with the potential, the triggering stress event doesn't happen. It can be many things but often it is a viral infection. Having said that, it is also the case that many, many people who eventually are diagnosed with celiac disease probably experienced the actual onset years before. Many celiacs are of the "silent" type, meaning that symptoms are largely missing or very minor and get overlooked until damage to the small bowel lining becomes advanced or they develop iron deficiency anemia or some other medical problem associated with celiac disease. Many, many are never diagnosed or are diagnosed later in life because they did not experience classic symptoms. And many physicians are only looking for classic symptoms. We now know that there are over 200 symptoms/medical problems associated with celiac disease but many docs are only looking for things like boating, gas, diarrhea. I certainly understand your concerns about not wanting to damage your body by taking on a gluten challenge. Your other option is to totally commit to gluten free eating and see if your symptoms improve. It can take two years or more for complete healing of the small bowel lining once going gluten free but usually people experience significant improvement well before then. If their is significant improvement in your symptoms when going seriously gluten free, then you likely have your answer. You would either have celiac disease or NCGS (Non Celiac Gluten Sensitivity).
    • catnapt
      after several years of issues with a para-gland issue, my endo has decided it's a good idea for me to be tested for celiac disease. I am 70 yrs old and stunned to learn that you can get celiac this late in life. I have just gradually stopped eating most foods that contain gluten over the past several years- they just make me feel ill- although I attributed it to other things like bread spiking blood sugar- or to the things I ate *with* the bread or crackers etc   I went to a party in Nov and ate a LOT of a vegan roast made with vital wheat gluten- as well as stuffing, rolls and pie crust... and OMG I was so sick! the pain, the bloating, the gas, the nausea... I didn't think it would ever end (but it did) and I was ready to go the ER but it finally subsided.   I mentioned this to my endo and now she wants me to be tested for celiac after 2 weeks of being on gluten foods. She has kind of flip flopped on how much gluten I should eat, telling me that if the symptoms are severe I can stop. I am eating 2-3 thin slices of bread per day (or english muffins) and wow- it does make me feel awful. But not as bad as when I ate that massive amnt of vital wheat gluten. so I will continue on if I have to... but what bothers me is - if it IS celiac, it seems stupid for lack of a better word, to intentionally cause more damage to my body... but I am also worried, on the other hand, that this is not a long enough challenge to make the blood work results valid.   can you give me any insight into this please?   thank you
    • trents
      The biopsy looks for damage to the mucosal lining of the small bowel from the inflammation caused by celiac disease when gluten is ingested. Once you remove gluten from the diet, inflammation subsides and the mucosal lining begins to heal. 
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