Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Confused by the gluten challenge?


elliespal

Recommended Posts

elliespal Newbie

Hi all,

I received a positive blood test for coeliac around 3 weeks ago and am currently awaiting my endoscopy appointment. 

I've been trying to explain and emphasise the seriousness of coeliac and how important it will be for me to be completely gluten free after the endoscopy (assuming it is positive). One thing that keeps cropping up is the question of; if gluten is so damaging to a coeliac to the extent that upon going gluten free I would need to worry about cross contamination etc, why am I allowed to continue eating gluten for the gluten test, especially without any monitoring from my current doctor? I do understand that the gluten challenge is a necessity for the endoscopy to understand the amount of damage and to receive an accurate diagnosis, however I'm finding it difficult to emphasise how poisonous gluten is for my system when it doesn't matter how much I currently consume?

On the same note, can anyone offer advice on how best to explain coeliac disease to family and friends in a way that makes them realise that this is more than an intolerance or lifestyle choice?

Thankful for any guidance on this strange journey ahead!

 


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master

This is a backward disease to dia, you have to keep eating to to show the damage....the more damage to be seen the more "oh this is bad"....the whole challenge in my opinion is to make it look as bad as can be for a positive dia....yeah stupid I know.
Open Original Shared Link
Depends on how you want to explain it....I have youtube videos to explain the disease to kids ....You can can simply say gluten is like drinking bleach/eating rat poison for my intestines. Or the more normal approach "My body treats the protein which is smaller then a germ and harder to clean off the keeping a CSI tech from finding blood, like a germ. And in creating antibodies to attack it, it also attacks and damages my intestines, (some people like me it can attack their nervous system and brain, or in the skin with DH). So any tiny and your own immune system (IE this is a autoimmune disease) will turn on your own body. SO gluten is very much like a bioweapon/poison to you and needs to be kept away from anything you eat, touch, or could get into your food (airborne flour, shampoos, lotion, etc.) Perhaps have them read the newbie 101 sections?
https://www.celiac.com/forums/topic/91878-newbie-info-101/

OH they do know this is genetic and anyone of them could have...or develop it later in life. And left untreated the damage caused can lead to other diseases, cancer, lymphoma, allergies, food intolerance, and in some cases like me brain and nerve damage that leave you with life changing disabilities and quirks.
 

 

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,246
    • Most Online (within 30 mins)
      7,748

    Shaxmom
    Newest Member
    Shaxmom
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.7k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • 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.
×
×
  • Create New...