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

Gluten Free But Not Celiac?


JustCan

Recommended Posts

JustCan Explorer

I just got my biopsy results and there's no evidence of celiac disease. But, after having done a gluten challenge, I know that gluten is poison for me and will definitely maintain a gluten free diet.

That said, while I'm happy the biopsy was negative, I'd still like some kind of proof that I'm gluten intolerant other than the diet itself.

Am I crazy? I'd love to hear from others that live gluten-free but aren't celiacs (wisdom from celiacs is welcome too :D) .


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



Celiac.com Sponsor (A8-M):



Guest j_mommy

It's totally possible that you have results from the diet!!!!

Were you gluten-free before your biopsy???? Did you do a gluten challenge prior to the biopsy if you were gluten-free????

Also remember that you can have false negatives with biopsies if they don't take enough samples!

All that said if the gluten-free diet is working for you, stay with it!!! Do whatever you need to to be healthy.

Have you had testing done for gluten intolerance???

JustCan Explorer
It's totally possible that you have results from the diet!!!!

Were you gluten-free before your biopsy???? Did you do a gluten challenge prior to the biopsy if you were gluten-free????

Also remember that you can have false negatives with biopsies if they don't take enough samples!

All that said if the gluten-free diet is working for you, stay with it!!! Do whatever you need to to be healthy.

Have you had testing done for gluten intolerance???

Thanks for your response! Yes, I was gluten-free before the biopsy and did a month long gluten challenge. I was really sick by the end of the month but there's no way to know if it was long enough. I also had bloodwork that was negative but I was gluten free at that time so it wasn't accurate. But no, I haven't been tested just for gluten intolerance. Is that the Enterolab test or is there another way?

Guest j_mommy

You're right on the part about length of gluten challenge.....there are standards but like celiac...I think it's different for everyone!

I would say your dietary response is enough of proof that you need to be gluten-free.

As for testing...I believe you could get that through entrolab....others will be able to comment on that more! i more knowledgeable about celiac than gluten intolereance!

Good Luck :D

gfpaperdoll Rookie

Dietary trial is the ultimate diagnosis, nothing else is really needed.

A negative biopsy just means that they did not see any abnormality in the tissue samples that they took. You could still have villi damage, it can be patchy & they might not have biopsied that area.

Also, the biopsy is up to the doc's interpretation, did he read it right????

I would not be betting my health on the result of anything as unreliable as a biopsy.

You can test thru Enterolab.com & see if you have a problem with gluten, diary... & get the gene test. I think the gene test is a real clue.

enterolab can just tell you if you have a problem with gluten not whether you are gluten intolerance or celiac, or allergic, well some people use the genes for that gauge, which is really not right either.

Anyway, good for you for figuring out that you are healthier gluten free.!!!

nmw Newbie

I had negative blood tests (had been gluten-free 2 weeks at the time), no biopsy and have been gluten-free for 16 months. Positive dietary response is all I need to confirm that for me, gluten is poison. My doc wrote "non-celiac gluten sensitive" in my chart. I don't feel the need to know anything beyond what I already know.

Dandelion Contributor

My bloodwork came back negative and my biopsy came back with no signs of damage, but my doctor lists me as gluten intolerant based on my dietary response. So I would say that dietary response is proof enough. I too was gluten free before I went to get the blood test and biopsy, but I felt so good that there was not a chance I would eat gluten again just for test results. I went from 9 years of feeling so ill that my general doctor had me tested for lyme disease, lupus, r.a., and cancer of every type to not feeling ill every single day.

If you do want to get other testing done there is also a company called Kimball Genetics that does it(blood and cheek swab). I know they were recently at the Gluten Free Vendor Fair at SUNY Farmingdale. I've never been tested by them, but did contact them for information and they seem very professional. Maybe somebody else on here has used them.


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



Celiac.com Sponsor (A8-M):



Guest Doll

If you feel better gluten free, (and all your tests checked out OK), stay gluten-free. My 2 cents.

andreagrant Apprentice

I had no signs of damage in the 2 (!) samples the GI doc took during my biopsy (and he was a jerk in person too). I went gluten-free anyhow, as my father and grandfather both have celiac and I was having classic symptoms. It's been 5 months and I feel like a new person--totally miraculous change (except the couple glutenings...). When I described my family history, symptom, and dietary response to my new house doctor (the old one got fired for reading my "negative" biopsy to me and suggesting I eat more WHEAT BRAN for my "IBS"), he wrote "celiac" in the chart and we moved on to the next topic. Even without that I would have stuck with it since I feel so good!

  • 2 weeks later...
CMCM Rising Star

I just attended a lecture by Dr. Fine of Enterolab. He discussed all this...so here's the bottom line, which MOST DOCTORS DO NOT UNDERSTAND!!!!

Think of gluten sensitivity as a SPECTRUM of reactions: at one end of the spectrum are those with zero observable symptoms. At the other end of the spectrum are very very sick individuals who OFTEN are diagnosed with celiac disease via biopsy. ONLY those with the celiac gene will end up with celiac disease. However, you do NOT have to have the celiac gene to be sensitive to gluten and to get very sick from it. The symptoms run the gamut of zero to horribly sick. There are some celiacs who have no symptoms. Some celiacs are terribly ill. Some people with gluten sensitivity (but no celiac gene) are just as sick as a sick celiac. And with or without the celiac gene, a gluten sensitive person can eat gluten and cause other auto-immune reactions.

There are a fair number of celiac specialists who are beginning to say it's probable that MOST, if not all Americans are at the very least gluten sensitive, and probably no one should eat gluten. Period.

Ultimately, we have to change the mindset of all this: Lacking a diagnosis of celiac disease (whichis after all, the worst end of the spectrum), you still must look at dietary response: If eating gluten makes you sick, it's probably doing damage to your body and you must stop eating it. If eliminating gluten makes you feel better, there's your answer. You don't need, I repeat, you DO NOT NEED a doctor to say you have celiac disease in order to follow the diet. Eventually, all this will be common medical knowledge, but right now it's not, unfortunately.

gfpaperdoll Rookie

YES, to CMCM's post ....

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 replied to McKinleyWY's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Accuracy of testing concerns

    2. - McKinleyWY posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Accuracy of testing concerns

    3. - trents replied to Teaganwhowantsanexpltion's topic in Introduce Yourself / Share Stuff
      4

      A little about me and my celiac disease

    4. - Peace lily replied to AristotlesCat's topic in Super Sensitive People
      118

      Gluten Free Coffee

    5. - Teaganwhowantsanexpltion replied to Teaganwhowantsanexpltion's topic in Introduce Yourself / Share Stuff
      4

      A little about me and my celiac disease

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

    • Total Members
      133,237
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • 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!
    • trents
      I know what you mean. When I get glutened I have severe gut cramps and throw up for 2-3 hr. and then have diarrhea for another several hours. Avoid eating out if at all possible. It is the number one source of gluten contamination for us celiacs. When you are forced to eat out at a new restaurant that you are not sure is safe, try to order things that you can be sure will not get cross contaminated like a boiled egg, baked potatos, steamed vegies, fresh fruit. Yes, I know that doesn't sound as appetizing as pizza or a burger and fries but your health is at stake. I also realize that as a 14 year old you don't have a lot of control over where you eat out because you are tagging along with others or adults are paying for it. Do you have support from your parents concerning your need to eat gluten free? Do you believe they have a good understanding of the many places gluten can show up in the food supply?
    • Peace lily
      Okay went online to check green mountain k cups .It was said that the regular coffees are fine but they couldn’t guarantee cross contamination.with the flavors. im trying to figure out since I eliminated the suyrup so far so good. I’m hoping. thanks it feels good to listen to other people there views.
    • Teaganwhowantsanexpltion
      Thank you I will i have been on a strict gluten free diet ever since I got diagnosed but sometimes places lie about there food so there r some things that do get contaminated which causes me to throw up on end for several hours until I can't hold myself up anymore 
×
×
  • 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.