Jump to content
  • 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

Hi From Me


wwebby

Recommended Posts

wwebby Apprentice

Hi everyone, I haven't visited this board in a year because I started to deny that I had a gluten problem last year and started eating gluten again. I even had Enterolab tests done last year and was positive for everything, so I don't know why I can't convince myself to stay gluten-free. I realized that I was doubting my own "self-diagnosis" and decided to go to a "real" gastroenterologist for the full Celiac blood panel and possibly an endoscopy. I guess I want the "real" diagnosis to get myself more committed to gluten-free and to make it easier to say to my friends and family that yes, I did go to a "real" doctor. I hate how people doubt this disease. And I hate how people call it an allergy! I am eating gluten right now because of the testing coming up, so my friend and I got a pizza last night and I said, "well, I have to eat some because I'm getting retested," and she said, "oh, yeah. I forgot about your little allergy." UGH! LITTLE ALLERGY??? But you know, I was the same way 10 years ago. I didn't understand why people couldn't have peanut butter from a jar that had bread crumbs in it. It seemed paranoid to me, but now I know better.

Anyway, I'm tired and cranky and gassy and itchy because of all the gluten I ate yesterday. I see the doc on the 29th. I wish they'd consider celiac testing an "emergency" and test us sooner than the weeks and weeks they make us wait--and eat gluten!


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



Celiac.com Sponsor (A8-M):



Guest jhmom

Hi wwebby (((((((hugs))))))))) to you!

I could not imagine eating gluten, even the slightest bit sends me to the moon! :( You poor thing, I do hope the testing is right around the corner and that you will not have to eat gluten much longer. BUT remember an improvement on a gluten-free diet is also a good test, even some docs will tell you that!

Hang in there and get better soon! :D

kejohe Apprentice

I second that, my son had positive blodd test and complete recovery on the gluten-free diet, so his doc decided the biopsy wasn't necessary and I am very thankful. I wholeheartedly believe that recovery on the diet is the biggest indicator for diagnosis there is.

Feel better soon!

plantime Contributor
your little allergy."  UGH!  LITTLE ALLERGY??? 

I had a woman call it "a little sensitivity" and tell me that eating whole wheat 4 or 5 times a day would cure it. A man kept trying to tell me that I could just take shots for it! I hope those people do not have to learn about it the hard way!

Guest gillian502

I agree with the annoyance of having a serious auto-immune disease mislabled as an "allergy." I try to calmly explain to people that the difference between an allergy and an auto-immune disease is: when you ingest something you're allergic to, your body attacks what you've just ingested. When you ingest something and you have an auto-immune disease, your body attacks ITSELF. That is the very nature of auto-immune. It drives me crazy that people can't at least be respectful of things even if they don't fully understand them!

terri Contributor

I'm traveling this week and all meals are being eaten in a restaurant. The servers and chefs have bent over backward to accomodate me and I haven't gotten sick at all. Yet. But, I am nervous about it.

mannabbe Newbie

Gillian,

I agree with your statements about "allergy" not representing our auto-immune condition - but what out Terri, who is eating out in restaurants all week? That's where the rubber hits the road for me - what do I say in a restaurant? My experience is that restaurant staff snap to attention when they hear the word "allergy" and that "gluten intolerance" and (rather controversially) "gluten allergy" are the operative words in the restaurant world.

If any of you have had experience making the whole "eating out" scene work in other ways, I would love to hear about it.

Terri, I just survived 10 days away from home and (miraculously!) returned home well. Yet another disaster averted - at least that's how it feels.

Laurie


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



Celiac.com Sponsor (A8-M):



terri Contributor

The restaurants here in Seattle have been incredible! I have my gluten free dining card which I laminated at Kinkos and last night the chef came to my table 4 times! They usually poach my salmon as that requires a special pan, and give me veggies and a salad. Last night the chef fried me some potatos and onions in the same pan as he backed my fish. For breakfast I've been ordering egg white omelets as that gets cooked in a pan and not a grill. Hard boiled eggs and fruit have worked out fine. Lunch has been the very hardest. Usually a salad with whatever grilled meat that is cooked over a flame that they have. I think I've lost 3 or 4 pounds this week though. Oh well, I'll have fun putting it on at home. Everyone feels sorry for me but they don't understand. I feel great! For the first time in years!! I've been gluten-free for 3 weeks now and what a difference!!!!!

mannabbe Newbie

Terri,

I live in Seattle - and I'd love to know the name of the restaurant you went to where the chef came to your table 4 times! I highly recommend Wild Ginger downtown - the majority of their menu is either already gluten free, or can easily be made gluten free. Also, try to make time for a trip to Flying Apron Bakery in the U District. You won't believe their gluten-free, vegan chocolate cupcakes.

happy travels, Laurie

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,664
    • Most Online (within 30 mins)
      7,748

    Lkscot0uky
    Newest Member
    Lkscot0uky
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Inkie
      Thank you for the information ill will definitely bring it into practice .
    • Scott Adams
      While plain, pure tea leaves (black, green, or white) are naturally gluten-free, the issue often lies not with the tea itself but with other ingredients or processing. Many flavored teas use barley malt or other gluten-containing grains as a flavoring agent, which would be clearly listed on the ingredient label. Cross-contamination is another possibility, either in the facility where the tea is processed or, surprisingly, from the tea bag material itself—some tea bags are sealed with a wheat-based glue. Furthermore, it's important to consider that your reaction could be to other substances in tea, such as high levels of tannins, which can be hard on the stomach, or to natural histamines or other compounds that can cause a non-celiac immune response. The best way to investigate is to carefully read labels for hidden ingredients, try switching to a certified gluten-free tea brand that uses whole leaf or pyramid-style bags, and see if the reaction persists.
    • Scott Adams
      This is a challenging and confusing situation. The combination of a positive EMA—which is a highly specific marker rarely yielding false positives—alongside strongly elevated TTG on two separate occasions, years apart, is profoundly suggestive of celiac disease, even in the absence of biopsy damage. This pattern strongly aligns with what is known as "potential celiac disease," where the immune system is clearly activated, but intestinal damage has not yet become visible under the microscope. Your concern about the long-term risk of continued gluten consumption is valid, especially given your family's experience with the consequences of delayed diagnosis. Since your daughter is now at an age where her buy-in is essential for a gluten-free lifestyle, obtaining a definitive answer is crucial for her long-term adherence and health. Given that she is asymptomatic yet serologically positive, a third biopsy now, after a proper 12-week challenge, offers the best chance to capture any microscopic damage that may have developed, providing the concrete evidence needed to justify the dietary change. This isn't about wanting her to have celiac; it's about wanting to prevent the insidious damage that can occur while waiting for symptoms to appear, and ultimately giving her the unambiguous "why" she needs to accept and commit to the necessary treatment. 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
      Welcome to the community! Generally, for a gluten challenge before celiac disease blood tests, Tylenol (acetaminophen) is considered safe and should not interfere with your antibody results. The medications you typically need to avoid are those like ibuprofen (Advil, Motrin) or naproxen (Aleve) that can cause intestinal irritation, which could potentially complicate the interpretation of an endoscopy if you were to have one. However, it is absolutely crucial that you confirm this with either your gastroenterologist or your surgeon before your procedure. They know the specifics of your case and can give you the definitive green light, ensuring your surgery is comfortable and your celiac testing remains accurate. Best of luck with your surgery tomorrow
    • Xravith
      Thank you for the advice. I’ve actually never checked for nutritional deficiencies, but for as long as I can remember, I’ve always taken vitamin and mineral supplements — otherwise my symptoms get worse. This week I stopped eating gluten to confirm whether my symptoms are really caused by it. Starting next week, I’ll reintroduce gluten — it’s sad to go back to how I was before — but at least I’ll be able to take the necessary tests properly. I think the diagnostic process will be long, but at least I’m happy that I finally decided to address this doubt I’ve had for years.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.