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

Puzzled


donnal

Recommended Posts

donnal Apprentice

My history includes having been tested for celiac with neg results (blood--had a scoping years before that and no abnorm cells were taken and tested). Well, I kept having gut issues as well as fatigue and a bad taste in my mouth and began reading about gluten-free diet so I went gluten-free back in April, then added corn-, soy-, dairy- and egg-free, adding back eggs which seemed OK. Each time I'd add back something, even gluten, I'd have mixed results (have been keeping a diary). So this past sund hubby and I went to Galveston for a couple of days and I ate everything wrong. On purpose. Well, the outcome was inconsistent. Some times I had pretty bad pain a/o bloating (up to 7 on scale of 0-10 once) but other times no problems. My main improvements, it seemed, on the diet were more energy, no bad taste in mouth, much less/very infreq gut issues (never D, always C has been the problem) but these didn't seem a problem on our time away (except, as stated above, sometimes gut issues). I have to factor in the point that there was no stress on this trip, whereas I have a fairly high level of stress normally. So, where does the diet fit in all this? Does the stress make the gut issues worse or is it possibly all stress related and not food issues at all, since I tested neg anyway (I know the tests aren't 100% reliable). My main concern is that if I have "borderline" gluten problems I don't want to make my body systems pay by eating it despite not having consistently evident "side effect". I am an RN so I know disease processes often don't manifest until damage is done and I don't particularly want that. On the other hand, there is no need to be trying to find appropriate foods if that is not really a problem. I thought maybe some of you out there might have some ideas of the directions I should head in now. Would it be "beneficial" to keep eating "wrong" until problems occur or should I just go back to G-, C-, S-, D- free limits? Thanks for any input!! DE


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

Have you considered having stool antibody testing? That may be helpful for you. Enterolab cannot diagnose celiac but they can tell you if you are forming antibodies to gluten, soy, casien, yeast and they can also measure the amount of fat to give you an idea if you are suffering malabsorption.

With the number of body systems effected by the antibody response it really is not a good idea to continue on gluten until you get severe symptoms if the diet is needed. There are some things that just may not be reverseable if you do that. Also US medicine unfortunately knows little about gluten impact on any system other than the gut. The risk is so high that it really would benefit you to avoid gluten if gluten is an issue.

YoloGx Rookie

There are some people who are gluten sensitive without having true celiac. You are right it could still cause degenerative disease(s). I think that if you feel better without it and the other grains etc. you seem to not tolerate well, avoid them. After a while you could challenge yourself again. It may be its OK for you to have these grains once in a while if you don't have true celiac. If you do, generally you will know it after you have been strictly off of the glutens for say 6 months.

The thing is however you could be getting trace glutens from other sources which would mask your response when you make the challenge. I was getting trace gluten from soap and shampoo and lotion for instance since vitamin E (tocopherol) in these products is usually made from wheat germ. Even animal food can be a source of this--so wash your hands after handling the food. And caramel color for instance is made from barley. Alcohol is usually made from grains so this too could be a source of constant exposure for you at work since alcohol is often used to clean equipment etc. Always use gloves! It made a huge difference for me to go off all this trace gluten stuff. There is a list here on Celiac.com of trace glutens in the home area that you can access. Then when I just got cross contaminated my response was D--which usually I never get. Like you its more C. Though not now being off all gluten.

For me it is worth being in this potentially more reactive state (if exposed to gluten) since without any of the glutens I no longer have joint problems and headaches and my eyes are not as sensitive. My energy too is growing in leaps and bounds and I am less subject to getting ill. If I do get exposed to trace gluten now I take probiotics or live sugar-free yogurt and pineapple or bromelain/papain right away to help counteract the immune response--and it really does help--that plus the following few days some detox herbs like dandelion, yellow dock and cleavers to deal with the resultant liver and lymph etc. toxicity and marshmallow root to soothe and heal the villi along with bromelain/papain which also takes down the inflammation.

It is said too that gluten isn't really that good for anyone since it is difficult to fully digest plus also due to the opiates involved, so avoiding it for the most part is good for everybody. The trick however is for you to figure out how strict and on the lookout that you need to be. Maybe you are lucky enough to be someone who really can feel better being off this stuff but can have it in a pinch or at someone's party now and then.

Good luck!

Bea

gfpaperdoll Rookie

My guess is that the "taste" in your mouth is from Barley. If that is the case you should really be careful. barley is in everything. As a nurse you should know how important the immune system is. That is what is altered when you eat gluten, with or without "symptoms".

I would like to invite you to our Houston celiac support group meetings. here is the link

Open Original Shared Link

not that they believes in gluten intolerance, but a lot of us know better & just overlook that ignorance.

donnal Apprentice
My guess is that the "taste" in your mouth is from Barley. If that is the case you should really be careful. barley is in everything. As a nurse you should know how important the immune system is. That is what is altered when you eat gluten, with or without "symptoms".

I would like to invite you to our Houston celiac support group meetings. here is the link

Open Original Shared Link

not that they believes in gluten intolerance, but a lot of us know better & just overlook that ignorance.

Thanks for the link!!! I went to it and found the Tyler group's email--I had heard there was a Tyler group (I live in East Texas) but didn't know how to find out about it!

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents commented on Scott Adams's article in Kids and Celiac Disease
      2

      New Study Reveals Age and Racial Gaps in Pediatric Celiac Testing

    2. - Russ H replied to pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Positive biopsy

    3. - Scott Adams replied to pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Positive biopsy

    4. - Scott Adams commented on Scott Adams's article in Latest Research
      3

      New "Glowing Bacteria" Pill Could Transform Gut Disease Detection (+Video)

    5. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      7

      Help understand results

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,001
    • Most Online (within 30 mins)
      7,748

    bonniebeebe143
    Newest Member
    bonniebeebe143
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Russ H
      What you describe is seronegative villous atrophy (negative antibody tests but positive biopsy). It is uncommon in coeliac disease, and there are other causes, but the most common cause is coeliac disease. I would pursue this with your healthcare provider if possible. Based on clinical history, test results and possible genetic testing for susceptibility to coeliac disease it should be possible to give a diagnosis. There is a bit more here: Seronegative coeliac disease
    • Scott Adams
      If you are still eating gluten you could get a celiac disease blood panel done, but I agree with @trents and the gold standard for diagnosing celiac disease would be your endoscopy results. Is it possible they did do a celiac disease panel before your biopsy? This would be the normal chain of events. 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.    
    • trents
      Actually, it would be more correct to say that the genetic potential to develop celiac disease is passed down from parents to children. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% of the general population actually do. But it is also true that the offspring of those who do have active celiac disease are at a considerably higher risk of developing active celiac disease than those of parents who have the genes but don't develop the disease. Some recent, larger studies put the risk at near 50% for the first degree relatives of those who have active celiac disease.
    • Jordan Carlson
      Hello everyone! Been a while since I posted. The past few moths have been the best by for recovery for myself. I have been the least bloated I have ever been, my constant throat clearing is almost gone, I have stopped almost all medication I was prevously taking (was taking vyvanse for adhd, pristiq for anxiety,fomotadine/blexten for histamine blockers and singulair). Only thing I take now is Tecta. I also no longer get any rashes after eating. Things are going very well. Most success came actually once I upped my B12 daily dose to 5,000 mcg. I do have one thing I am un able to figure out and want to see if anyone else has this issue or has experience working around it. Ever since I was born I have always had a issue getting fruits and veggies down. No matter how hard I tried, it would always result in gagging or throwing up. Always just thought I was a picky eater. Now that my stomach and system has healed enough that I can feel when something is off almost istantly, I notice that after eating most fruits (sometimes I am ok with bananas) and veggies, my stomach instantly starts burning and my heart starts to pound and I get really anxious as if my body doesnt know what to do with what just enetered it. So I am thinking now that this is what probably was going on when I was born and my body started rejecting it before which caused this weird sensory issue with it causing the gagging. Hoping someone has some exprience with this as well because I would love to be able to enjoy a nice fruit smoothie once in a while haha. Thanks everyone!
    • wellthatsfun
      i know i've been rather cynical and sad about being fully diagnosed in june 2025, but my boyfriend has been consistently showing me the wonderful world that is gluten free cooking and baking. in the past couple of days he's made me a gluten free rice paper-wrapped spanakopita "pastry", plus a wonderful mac and cheese bechamel-ish sauce with gluten free pasta (san remo brand if you're in australia/if you can get your hands on it wherever you are).  those meals are notably gluten free, but mainly he's been making me easy gluten free meals - chili mince with white rice and sour cream, chicken soup with homemade stock from the chicken remains, and roast chickens with rice flour gravy and roast veggies. i'm a bit too thankful and grateful lol. how lucky could i possibly be? and, of course, for those who don't have someone to cook for them, it's quite easy to learn to cook for yourself. i've been making a lot of meals for us too. honestly, cooking is pretty darn fun! knowing basic knife skills and sanitary practices are all you really need. experimenting with spices will help you get on track to creating some really flavourful and yummy dishes. coeliac is a pain, but you can use it to your advantage. healthier eating and having fun in the kitchen are major upsides. much luck to all of you! let's be healthy!
×
×
  • 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.