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Gluten-Free Foods, Products, Shopping & Medications

Share info on about GF products, medications, cosmetics, etc., or warn others about dangerous ones. Which ingredients are safe and which are not? Food labeling issues and legislation.


18,513 topics in this forum

  1. SabrinaLuvsGluten
    Emme999
    • 4 replies
    • 4.7k views
  2. Guest Addicted2Gluten
    KaitiUSA

    Gluten Free Shaving Creams

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  3. anerissara
    Guest
    • 7 replies
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  5. Guest Leidenschaft
    rma451

    Awesome Noodle Bowl!

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    • 3.9k views
  6. Wandering Hermit
    calico jo
    • 17 replies
    • 7k views
  7. mytummyhurts
    celiac3270
    • 18 replies
    • 2.8k views
  8. 12bGF
    lotusgem
    • 4 replies
    • 2.2k views
  9. jknnej
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  10. rmmadden
    lovegrov
    • 1 reply
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  12. Guest BERNESES
    mommida

    Gluten Free Hair Color?

    • 1 reply
    • 4.3k views
  13. kvogt
    jenvan
    • 3 replies
    • 1.4k views
  14. beelzebubble
    celiac3270
    • 5 replies
    • 3k views
  15. Guest GFLisa0405
    Guest

    Chi Chi's Salsa

    • 1 reply
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  16. Guest gliX
    angel-jd1

    Mcdonalds Salads

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    • 5.6k views
  17. beks
    plantime
    • 2 replies
    • 6k views
  18. mela14
    • 7 replies
    • 1.9k views
  19. tammy
    • 0 replies
    • 1.7k views
  20. Guest gillian502
    Guest

    Vick's Nyquil

    • 9 replies
    • 23.9k views
  21. SabrinaLuvsGluten
    tammy
    • 7 replies
    • 26.1k views
  22. gills29
    celiac3270
    • 9 replies
    • 1.8k views
  23. jaimek
    stef-the-kicking-cuty
    • 15 replies
    • 5.9k views
  24. HAPPY DOG SUZ
    • 0 replies
    • 1.2k views
  25. mytummyhurts
    • 9 replies
    • 4.5k views
  26. jknnej
    lovegrov

    Wine

    • 3 replies
    • 1.4k views
  27. sdore

    Vitamins

    • 2 replies
    • 1.3k views

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  • Posts

    • Scott Adams
      Thanks for sharing this! Here is more info about those cookies: https://partakefoods.com/collections/cookies 
    • Scott Adams
      According to their site: https://shop.hersheys.com/our-brands/reeses/034000943265.html
    • Scott Adams
      The positive Anti-deamidated Gliadin IgA result (12 U/ml) suggests possible celiac disease, but it is not definitive on its own, as this marker can also be elevated in other conditions or even in non-coeliac gluten sensitivity (NCGS). Do you know if they also ran a tTg-Iga test? This is the definitive test for celiac disease. The absence of classical symptoms like significant bloating or pain upon gluten reintroduction, along with your history of IBS and sensitivity to legumes, complicates the picture (legumes can be cross-contaminated with wheat). While celiac disease remains a possibility, other conditions like NCGS, leaky gut, or additional food intolerances could also explain your symptoms. A biopsy would provide more conclusive evidence for celiac disease, but for that you need to be eating lots of gluten daily in the weeks leading up to the endoscopy. In the meantime, adopting a gluten-free diet and supporting gut health with supplements (e.g., probiotics, L-glutamine) may help reduce inflammation and symptoms, but it’s important to consult a healthcare professional to tailor your approach and rule out other underlying issues. This article might be helpful. It breaks down each type of test, and what a positive results means in terms of the probability that you might have celiac disease. One test that always needs to be done is the IgA Levels/Deficiency Test (often called "Total IGA") because some people are naturally IGA deficient, and if this is the case, then certain blood tests for celiac disease might be false-negative, and other types of tests need to be done to make an accurate diagnosis. The article includes the "Mayo Clinic Protocol," which is the best overall protocol for results to be ~98% accurate.    
    • Scott Adams
      You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Liquid lunch
      I don’t think it matters much, there’s another type of cordyceps but I’m not sure if there’s a lot of difference, the one I’m using is cordyceps sinensis from maesyffin in wales, sinensis is the one with a long history of medicinal use in china. I think the alcohol (vodka) in the tincture helps with uptake vs taking capsules. And yes, changing my diet helped but it’s almost impossible to maintain as I can’t eat any lectins or sugar which is almost everything. Low lectin is about the best to hope for, they’re in everything. I can eat teff, millet, hemp seeds, blueberries, strawberries, blackcurrants, yogurt, cheese, walnuts, pistachios, macadamia, Brazil nuts, broccoli, sweet potato, carrots, beetroot, olives, rocket, onions, garlic, avocado, kale, mushrooms, chlorella/spirulina, and fish. That’s about it. I keep quail and make their food myself because lectins get into the commercial pellet fed chickens eggs. It took me years of adding one thing at a time with three weeks of pain every time I got it wrong to figure this out but there’s a finger prick blood test available now that will tell you which foods are triggering your autoimmune system, they test for 200+ different proteins and measure igg and ige antibodies. Good luck, I hope the mushrooms help but best to address the cause of the problem I think and have the igg and ige antibody test. The test won’t work if you’re already taking the mushrooms.
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