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.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    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

    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
    • Scott Adams
      Is this the same restaurant? https://www.facebook.com/TheHappyTartFallsChurch/ Is it too late to take this up with your credit card company? Normally you have a few months to do a chargeback with them. It seems very odd that they are taking this approach with someone who is likely to be a regular customer--not a good business-minded way of handling things!
    • Scott Adams
      Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs. Because of this it took me decades to overcome a few long-standing issues I had that were associated with gluten ataxia, for example numbness and tingling in my feet, and muscle knots--especially in my shoulders an neck. Only long term extensive supplementation has helped me to resolve these issues.        
×
×
  • 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.