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Finally Getting Somewhere!


Ox on the Roof

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Ox on the Roof Apprentice

So, I don't have an official diagnosis, and my IgG and IgA blood work was negative. But why else would I be doing so well when I am cooking gluten-free at home - for a month now - and then get sick every time I eat out and make "educated guesses"?

After reading a bunch of stuff about McDonald's fries, I decided to give them a go. Within an hour, I started with the upper GI symptoms. I sound like Buddy the Elf after he drank the soda! Pepto Bismol is my friend. (A big THANKS to whoever gave me that suggestion!) Of course, I also had the Bacon Ranch salad with no chicken. So I am not sure exactly what the culprit was, but it was definitely something I ate.

Official diagnosis or no, gluten intolerance or Celiac, WHATEVER...I cannot eat gluten! It's a good feeling to finally get a clue as to what's been wrong with me for almost two years. Now, if I can just learn how to eat out without getting sick!


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mushroom Proficient

Well, can you try not eating out for a while, until you master the diet and learn all the hidden sources of gluten first? Then you can start figuring out how the restaurants can cross-contaminate you :P

GFinDC Veteran

Sounds like you are getting somewhere with your diet changes at home. It doesn't matter a whole lot what it's called, celiac or gluten intolerance, if it makes you sick then staying away from it is the right thing to do. Congrats on getting some food traps figured out! :)

Skylark Collaborator

I've given up on making educated guesses eating out. Either the restaurant has a gluten-free menu or I don't go there.

Ox on the Roof Apprentice

mushroom, I am starting to think that's the best way to go. My family usually eats out once a week with my in-laws. It's like Russian roulette! My family is very supportive, but I've been sick for so long that I hate imposing on them. But my new thought is that it isn't imposing on ANYONE to just have something to drink and maybe a plain baked potato, then eat when I get home.

gluten-free - thanks! It's WONDERFUL to feel better! Today marks one month gluten-free, and after tomorrow I will have survived the two biggest holidays (Thanksgiving was day one).

Skylark - I hear ya! With McD's, well...I don't even like that place, but they have an indoor playground, which is nice for my kids when it's freezing outside. I checked their website before I left and thought I was doing good, but my first bite of French Fry tasted weird to me. After about six fries, I realized that they tasted like McNuggets! I think they were fried together. At least it only lasted that night.

tea-and-crumpets Explorer

I've given up on making educated guesses eating out. Either the restaurant has a gluten-free menu or I don't go there.

I'm pretty much the same way. I have found that I trust chains (PF Changs, Biaggi's) more than I do local places, though -- I ate off the gluten free menu at a local place and got really sick. I feel like chains are more afraid of legal action so they really train their staff. I might be crazy, but it has worked for me so far.

Juliebove Rising Star

We do eat out a lot, but... We eat at the same places. We have food allergies, not celiac. We try to find places that cook the food from scratch (for the most part anyway). We tell them of our food allergies and they cook special meals for us. Often we order side dishes that we know are safe (except perhaps for cross contamination) such as canned or fresh fruit, bacon, cottage cheese, Hormel chili (not scratch, but safe) or in the case of a place like McDonalds, only the prepackaged items like the apple slices.

We do also eat at places with gluten-free menus.


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    • trents
      Welcome to the celiac.com community, @McKinleyWY! There currently is no testing for celiac disease that does not require you to have been consuming generous amounts of gluten (at least 10g daily, about the amount in 4-6 slices of wheat bread) for at least two weeks and, to be certain of accurate testing, longer than that. This applies to both phases of testing, the blood antibody tests and the endoscopy with biopsy.  There is the option of genetic testing to see if you have one or both of the two genes known to provide the potential to develop celiac disease. It is not really a diagnostic measure, however, as 30-40% of the general population has one or both of these genes whereas only about 1% of the general population actually develops celiac disease. But genetic testing is valuable as a rule out measure. If you don't have either of the genes, it is highly unlikely that you can have celiac disease. Having said all that, even if you don't have celiac disease you can have NCGS (Non Celiac Gluten Sensitivity) which shares many of the same symptoms as celiac disease but does not involve and autoimmune reaction that damages the lining of the small bowel as does celiac disease. Both conditions call for the complete elimination of gluten from the diet. I hope this brings some clarity to your questions.
    • McKinleyWY
      Hello all, I was diagnosed at the age of 2 as being allergic to yeast.  All my life I have avoided bread and most products containing enriched flour as they  contain yeast (when making the man made vitamins to add back in to the flour).  Within the last year or so, we discovered that even whole wheat products bother me but strangely enough I can eat gluten free bread with yeast and have no reactions.  Obviously, we have come to believe the issue is gluten not yeast.  Times continues to reinforce this as we are transitioning to a gluten free home and family.  I become quite ill when I consume even the smallest amount of gluten. How will my not having consumed breads/yeast/gluten for the better part of decades impact a biopsy or blood work?  I would love to know if it is a gluten intolerance or a genetic issue for family members but unsure of the results given my history of limited gluten intake.   I appreciate the input from those who have gone before me in experience and knowledge. Thank you all!
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