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Celiac Disease Pre-Diagnosis, Testing & Symptoms

If you haven't yet been diagnosed this is the place you can discuss your symptoms and any test results that may indicate that you might have the disease.


19,067 topics in this forum

  1. LoopyLou
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  2. Fourgifts
    cyclinglady
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  5. sgm405
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  6. chocolatesunrise
    cyclinglady
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  7. LondonJules1
    Ennis-TX
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  8. VLH
    Beverage
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  12. Marie1976
    1888
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  13. Basslover
    Rweber
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  14. Hayley-1982
    cyclinglady
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  15. Christy71
    squirmingitch
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  16. Jefferson Adams
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  17. rowanie
    chocolatesunrise
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  18. marynrandy
    cyclinglady
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  19. Matt C
    GFinDC
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  20. GlutenFreeRegerts
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  21. Chase80
    Keight
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  22. Keight
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  23. Z4CH
    Awol cast iron stomach
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  24. pinkpandapants
    MaryinAz
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  25. Tracey E
    Scott Adams
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  26. LBell-Aus
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  27. Solafide3
    squirmingitch
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  • Recent Activity

    1. - Chrissyjo replied to Chrissyjo's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
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      I think I’ve got it ?

    2. - Jodi Lee K posted a topic in Related Issues & Disorders
      0

      Celiac and Styes

    3. - Jake R. replied to Jake R.'s topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
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      Newly Diagnosed

    4. - trents replied to MG1031's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      5

      13 y/o new celiac dx and joint pain

    5. - trents replied to Jake R.'s topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
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      Newly Diagnosed


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  • Posts

    • Chrissyjo
      Thanks all for your replies. I ended up having my gastrocopy last week. I did get a biopsy done for celiac. The man who did the test was sure I didn’t have it so we will see what the result is 
    • Jodi Lee K
      Hi. I have known I have Celiac disease coming up on 2 years. I have never had problems with styes before my diagnosis. I can no longer wear makeup without waking up the next day with horrible painful swelling in part of my eye lid. (at least one) I’ve been to many doctor and specialist appointments over it and they just say to wash my face more. I’m  looking for safe makeup product recommendations? Has anyone had an experience similar? What other things should I watch out for? 
    • Jake R.
      I did some reading from the link you posted and will definitely use the information provided to my advantage! I feel very lucky with my current situation, as my family has been very supportive as well as my closer friend-group. I appreciate the welcome and the information!
    • trents
      By the way, B12 is necessary for the uptake of iron. B12 deficiency is extremely common in the celiac population and, of course, plugs right into the fact of anemia also being extremely common in the celiac population. Some people have a form of anemia known as pernicious anemia in which the anemia is caused by the death of the parietal cells in the stomach. The parietal cells are where "intrinsic factor" is produced, an enzyme necessary for the absorption of B12 which, in turn, is necessary for the absorption of iron from the diet.
    • trents
      Welcome to the forum, @Jake R.! First of all, kudus to the doc who ordered the test checking for celiac disease based on the family history of it. Many in the celiac population suffer for many years before getting a proper diagnosis and that despite have classic GI symptoms. I will embed an article that you might find helpful in polishing your efforts to eat gluten free as there can be quite a learning curve involved. Some of this may be overkill unless you are a super sensitive celiac. Gluten is hidden in many food products where you would never expect it to be found and then there is the whole challenge of CC (Cross Contamination), particularly when dining out.    But let me caution you about the falling of the "other shoe", so to speak, of finding out you have celiac disease. There is this great sense of relief at the front end of the experience in finally discovering what what wrong with you that was causing so much distress and discomfort. But then it begins to dawn on you that having celiac disease has a social cost to it. You can't just accept spontaneous invitations to go over to friends or family's homes for dinner or to go out to their favorite restaurants to eat with them. Some of them simply will not understand or believe that this is a real medical problem and that you must avoid all gluten in order to guard your health and be safe. You may begin to feel like a fifth wheel at social gatherings and it may cost you some friendships. I'll embed an article link on one person's commentary about this phenomenon. Just a heads up.        
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