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  1. knitty kitty

    knitty kitty

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    ALBANICKAP

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    Sicilygirl

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Showing content with the highest reputation on 01/30/2025 in all areas

  1. badastronaut
    Thanks very much for the in depth reply!!! I'll discuss it with my doctor next week!
    1 point
  2. Jordan23
    I would stop Xanax. It will eat away at your DAO enzymes needed to break down histamine . No energy drinks will do the same. I use to have all reactions in stomach now it's changed and started in my chest , which completely sucks and bummed. Maybe your reacting to high histamine foods. But it's hard to avoid cross contamination. I would get pea milk made...
    1 point
  3. TerryinCO

    New Guy Here...

    I haven't been on the site for a while and I have some update info. Genetic tests show I have the Celiac markers and high risk for Celiacs's (10X it shows). Immoglobulin A and G are low - just below the 'green' range; immoglobulin M is in the 'green'. Zinc, Iron, magnesium, ferritin, and b12 are all in the 'green' range. I've been off the PPI...
    1 point
  4. ALBANICKAP
    Thank you Scott, I will try what u suggested.
    1 point
  5. knitty kitty
    Hi, @Sicilygirl, I had lost a great amount of weight, felt depressed, and had no appetite early on. I found that taking Thiamine in the form Benfotiamine extremely helpful. Doctors routinely check B12 and Vitamin D, but they fail to test for deficiencies in other B vitamins like Thiamine, because blood tests for other vitamins are not accurate...
    1 point
  6. Sicilygirl
    Hello Scott, I did lose weight at the beginning of diagnosis and I know that it will take time to put on the weight I did lose. I think I have no appetite because this has been a roller coaster of emotions and a Big change on my body and its out of whack mentally and pysically. I think I am just depressed to be honest.
    1 point
  7. knitty kitty
    @Soleihey, Do get checked for thiamine deficiency. Blood tests for thiamine deficiency are not accurate. You can have "normal" levels in the blood, but still be deficient because thiamine stores inside cells are depleted. Thiamine deficiency can cause ataxia, tremor, muscle twitching, leg weakness, constipation, and slurred speech. I had these...
    1 point
  8. knitty kitty
    Thiamine supplementation will help this "air hunger" . It's known as "sailors' asthma" because sailors used to get thiamine deficiency at sea without fresh meat. Thiamine Hydrochloride supplements will help. So will Allithiamine, so called because it is derived from plants in the Alum family, onions and garlic. Benfotiamine will also help.
    1 point
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    • trents
      Welcome to the forum, @Emma2322! Can you give us some context here? This online community exists to support those with gluten-related disorders such as celiac disease and gluten sensitivity. Does your cousin suffer from a gluten-related disorder?
    • trents
      Welcome to this online community, @Mina H! 1. Apart from any consideration of crypt hyperplasia, villous atrophy is the hallmark of celiac disease. There are some other things that can cause villous atrophy such as an intolerance to cow's milk protein (CMP), chronic NSAID use, a certain blood pressure med, certain parasitic intestinal infections and a few other medical conditions but they are relatively unlikely compared to celiac disease being the cause, especially in view of the accompanying symptoms you list. 2. The endoscopy with biopsy is still considered to be the gold standard of celiac disease diagnosis, not blood antibody testing. Blood antibody testing is in some ways the "rule out" step for determining whether or not to move on to the second and more definitive stage of diagnosis, namely, the endoscopy/biopsy. There is a movement afoot to diagnose celiac disease based on blood antibody testing alone but only when the TTG-IGA score reach 10x mormal. 3. All the symptoms you describe are classic and scream of celiac disease. If your healthcare system in Japan is unable or unwilling to grant you an official diagnosis based on the biopsy results and your symptoms, your next step would be to engage with the gluten free diet and see if your symptoms improve over a period of weeks/months.
    • Emma2322
      My name is Emma and I'm 36. I am here to learn about IVF treatment because my cousin is going to do her IVF but I heard from many people it's very hazardous. Could anybody tell me if she should go for treatment or not?
    • Mina H
      Hi. My biopsy results just came back and it's a little confusing. Here's what the report says (I translated it myself from Japanese): Biopsy report -Chronic duodenitis -The mucosa shows mild to moderate lymphocytic infiltration, and the villi are partially shortened and atrophic. -Mild lymphocytic infiltration is seen in the surface and crypt epithelium. -Crypt hyperplasia is not clearly present, but the findings are considered not inconsistent with celiac disease. (My note: Japanese people like this kind of statement) -No findings of granulomas, specific infectious disease, or malignancy are observed   The GI said he didn't see anything special during the upper endoscopy but sent samples (not sure how many samples he took) for biopsy. 1. So, my question is, does the biopsy report makes sense? (Villi atrophy and lymphocytes are present, but no clear crypt hyperplasia? Can it still be considered MARSH 3a (because of villi atrophy?) and therefore suggestive of Celiac?   I have to say, althought not completely gluten free, recently, I've been trying to avoid gluten when cooking for myself but I would eat pizza or cheese cake or cookies or pasta now and then, maybe at least one-two times a week. I'm quite shocked because ever since I learned that I have a Celiac gene, althought not strict complete gluten free, I really tried not to eat bread or pasta or pizza every meal or everyday (even changed my soy souce to flour-free Tamari sauce), but it was enough to damage the villi. I think many Asian condiments contain gluten, even some vinegar in Japan... 2. Another question is the biopsy result alone enough to confirm I am Celiac, since getting a blood test is not readily available and expensive to do in the country I'm living in (Japan)? Or should I continue eating gluten and wait 8 weeks and pay out-of-pocket for the antibodies test too (super expensive to me though ($500 USD, even endoscopy is practically free/cheap here) because the blood draw will be done by a clinic in Tokyo, but the sample has to be sent to a US lab)? Hoever, I live very far from Tokyo or large cities so there will also be travel costs. *** Background Info: I'm Asian female living in Japan where Celiac is thought to be very rare, so the blood test for antibodies is not readily available even through doctors. I'm not Japanese, by the way. I learned several years ago that I am HLA-DQ2.5 positive (heterozygous). Symptoms: Recently, I've been feeling off whenever I ate something with gluten. But the symptoms were vague like having to run into bathroom, constipation (I suppose more constipation than diarrhea), brain fog/dizziness, tiredness/daytime sleepiness, gassy/bloating or cramps, random abdominal pain (I thought it was due to ovulation or something). I thought it was IBS or something. I also had acid reflux sometimes, successfully controlled or healed through acid watcher's diet etc. The most problematic symptom for me was acid reflux or LPR/silent reflux (I did a Peptest and there was pepsin detected in my saliva even when I didn't particularly felt heartburn!), I thought it was because I ate dark chocolate and drank spearmint tea everyday so stopped. Reflux is why I went to the GI to ask for uppper endoscopy.
    • trents
      Welcome to the forum, @Terrance Donald! Are you actually allergic to gluten or do you say that meaning you either have celiac disease or NCGS (Non Celiac Gluten Sensitivity), neither of which are allergies?
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