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Really Bad Breath, Worse On Gluten


Meg123

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Meg123 Explorer

I have had ongoing, permanent bad breath (my little children always tell me) since going gluten light,(after a period of gluten free) and have noticed it's been getting worse, but much much worse since doing this challenge.

I am also aware it's a sign of candida infection. I was just wondering if any one else noticed that they had bad breath when on gluten and then it got better when they went gluten free? Or if it is a known sign of celiac disease / gluten intolerance. I haven't seen it on any lists of symptoms anywhere, but often real peoples experiences are the best ....

thanks


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dilettantesteph Collaborator

I've been off gluten three years now, but your post reminded me. It was an issue for both my son and I. We were diagnosed at the same time. We don't notice it now, even when we get glutened, so I'd forgotten all about it. Hopefully it will go away for you too.

sreese68 Enthusiast

I read something about bad breath on a food intolerance list I'm on. One person mentioned that diabetes can cause odor. Another mentioned this link: Open Original Shared Link (low carb diet causing bad breath) I personally don't know anything about this topic, but thought I'd forward this info in case it helps...

mommida Enthusiast

Eosinophilic Esophagitus also causes bad breath. Have you noticed and creamish/ white spots on your tonsils? It smells like puss.

Diebetic ketosis smells like acetone (an ingredient in nail polish remover)

Sinus problems, candida overgrowth, food intolerances/ GI problems, and dry mouth/dental issues can also be a factor.

It is a reason to see a doctor.

Kate79 Apprentice

I think bad breath can definitely be a gluten intolerance/celiac symptom. I never realized I had an issue with bad breath until my fiancee told me about it. According to him, it's only present when I've had gluten and my breath is normal when I'm gluten free - which I've been for about 9 months now. He can tell if I've had any accidental gluten by my breath (in addition to my other symptoms - mostly bloating and migraine). Anyway, he says it smells 'like something crawled down my throat and died'. Yikes!

  • 6 months later...
daddys-girl Newbie

Yes.. I am experimenting the same thing.. I have not been diagnosed with Celiac but I have PCOS and decided to try going Gluten free because I heard that it may jump start my cycle on it's own..

But I did notice that my breathe is fresher.. I had a deep cleaning and it didn't help.. So I thought that my case was more severe.. But I guess my body isn't able to handle Gluten very well., I have been Gluten free for about a week or so.. Thank u for your post!!

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    • trents
      Not necessarily. The "Gluten Free" label means not more than 20ppm of gluten in the product which is often not enough for super sensitive celiacs. You would need to be looking for "Certified Gluten Free" (GFCO endorsed) which means no more than 10ppm of gluten. Having said that, "Gluten Free" doesn't mean that there will necessarily be more gluten than "Certified Gluten" in any given batch run. It just means there could be. 
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      I think it is wise to seek a second opinion from a GI doc and to go on a gluten free diet in the meantime. The GI doc may look at all the evidence, including the biopsy report, and conclude you don't need anything else to reach a dx of celiac disease and so, there would be no need for a gluten challenge. But if the GI doc does want to do more testing, you can worry about the gluten challenge at that time. But between now and the time of the appointment, if your symptoms improve on a gluten free diet, that is more evidence. Just keep in mind that if a gluten challenge is called for, the bare minimum challenge length is two weeks of the daily consumption of at least 10g of gluten, which is about the amount found in 4-6 slices of wheat bread. But, I would count on giving it four weeks to be sure.
    • Paulaannefthimiou
      Are Bobresmill gluten free oats ok for sensitive celiacs?
    • jenniber
      thank you both for the insights. i agree, im going to back off on dairy and try sucraid. thanks for the tip about protein powder, i will look for whey protein powder/drinks!   i don’t understand why my doctor refused to order it either. so i’ve decided i’m not going to her again, and i’m going to get a second opinion with a GI recommended to me by someone with celiac. unfortunately my first appointment isn’t until February 17th. do you think i should go gluten free now or wait until after i meet with the new doctor? i’m torn about what i should do, i dont know if she is going to want to repeat the endoscopy, and i know ill have to be eating gluten to have a positive biopsy. i could always do the gluten challenge on the other hand if she does want to repeat the biopsy.    thanks again, i appreciate the support here. i’ve learned a lot from these boards. i dont know anyone in real life with celiac.
    • trents
      Let me suggest an adjustment to your terminology. "Celiac disease" and "gluten intolerance" are the same. The other gluten disorder you refer to is NCGS (Non Celiac Gluten Sensitivity) which is often referred to as being "gluten sensitive". Having said that, the reality is there is still much inconsistency in how people use these terms. Since celiac disease does damage to the small bowel lining it often results in nutritional deficiencies such as anemia. NCGS does not damage the small bowel lining so your history of anemia may suggest you have celiac disease as opposed to NCGS. But either way, a gluten-free diet is in order. NCGS can cause bodily damage in other ways, particularly to neurological systems.
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