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 induced body odor?


justwantcure

Recommended Posts

justwantcure Newbie
(edited)

Hi everyone, I'm getting a blood test for Celiac next week, but I've been dealing with this really embarrassing problem and it's really made my life difficult. For the past 2 years I've had strong body odor, described as fecal/sulfur like. This body odor only began when I was hired to work in a bakery (it's so gross, I'm sorry). Before this I've been on long plane rides and out in public with no complaints, but now it's impossible for me to even go to the movie theater.

 

I've seen ENTs for this, dentists, etc. -- no tonsil stones, gum disease, cavities. No doctors seem to have any idea what this could be. My only clue is it began when I started working at the bakery, and I'm constantly inhaling gluten for hours each day. The weird thing is I can't smell this on myself but everyone around reacts the same, so it has to be from me. Also forgot to mention, I had a blood panel done to see if it could be diabetes - and it came back with a severe B12 deficiency and vitamin D deficiency. My doctor said the normal level for B12 should be 1200, but mine was at 200.

 

Has anyone here dealt with something similar? I'm not sure what else I can do. I know for a fact it's not TMAU since my in-laws reacted to me recently, but before that I would see them often and there was no complaints about any smells. And I traveled a lot on planes before all of this too (maybe 6 or more times a year) and there was zero reactions.

Edited by justwantcure
important detail added

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



Celiac.com Sponsor (A8-M):



Scott Adams Grand Master

There are others who have posted on this topic, and these links might help:

 

Awol cast iron stomach Experienced

Hi i don't recall that I had a smell per se. I do know that after detoxing after the Gluten challenge. I was sweating out at night rest time as if I was running a high fever from illness. My husband even noticed it was unusual.

Are you still working at the bakery? Did you finish all your celiac testing?

If so then my opinion would be to support your body in detoxing and support your gi tract in replacing microflora-probiotic to hopefully get back your homeostasis and natural scent.  It's possible your body was actively fighting hard with constant exposure at the bakery to detox any inhalation\ possible ingestion.  I am not a Dr but someone with gi issues and  DH who went a long time misdiagnosed. I went alternative routes to cope with whatever I had that didn't seem to be fixed by my former misdiagnosis'.

It sounds like you are on right track getting that vitamin d deficiency and b12 issue addressed. 

For me I use several ways to detox depending on what feels right for you

Drinks tons of water

Dandelion tea

Acupuncture

Epsom salt bath

Exercise

Many of these help me you could find the one that works best for you or a combination of them. 

Best wishes

Posterboy Mentor
On 4/18/2019 at 11:28 AM, justwantcure said:

Hi everyone, I'm getting a blood test for Celiac next week, but I've been dealing with this really embarrassing problem and it's really made my life difficult. For the past 2 years I've had strong body odor, described as fecal/sulfur like. This body odor only began when I was hired to work in a bakery (it's so gross, I'm sorry). Before this I've been on long plane rides and out in public with no complaints, but now it's impossible for me to even go to the movie theater.

 

I've seen ENTs for this, dentists, etc. -- no tonsil stones, gum disease, cavities. No doctors seem to have any idea what this could be. My only clue is it began when I started working at the bakery, and I'm constantly inhaling gluten for hours each day. The weird thing is I can't smell this on myself but everyone around reacts the same, so it has to be from me. Also forgot to mention, I had a blood panel done to see if it could be diabetes - and it came back with a severe B12 deficiency and vitamin D deficiency. My doctor said the normal level for B12 should be 1200, but mine was at 200.

 

Has anyone here dealt with something similar? I'm not sure what else I can do. I know for a fact it's not TMAU since my in-laws reacted to me recently, but before that I would see them often and there was no complaints about any smells. And I traveled a lot on planes before all of this too (maybe 6 or more times a year) and there was zero reactions.

justwantcure,

I don't know if this will help you are not ...but it is worth a shot.

There  is a genetic condition than cause you to smell like rotting fish.

https://www.medicinenet.com/fish_odor_syndrome_trimethylaminuria/article.htm#how_do_people_inherit_fish_odor_syndrome_trimethylaminuria

You said B.O. but are you sure it's not your breath?

I used to have an ulcer (being undiagnosed) that caused a condition called "dragon breath" or bad breath on steroids....my friends would tell me I had bad breath ...despite brushing my teach regullarly.

https://www.sciencedaily.com/releases/2008/11/081123222846.htm

It was bad enough ...I could cup my hand and test my breath for it's smell and I was repulsed by the smell and when I have encountered other's with dragon breath ....I can usually tell them it' an ulcer (I can stand 10 feet away) and still smell their breath....It is quite an abnormal thing.

Bad breath is also known as Halitosis ...but when it is ruining your life...it is probably most likely from an ulcer and you don't know you have one.

try buying your some mastic gum ...it really works wonders for ulcers.

https://www.dailymail.co.uk/health/article-97549/A-gum-cure-stomach-ulcers.html

I hope this is helpful but it is not medical advice.

Posterboy,

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,893
    • Most Online (within 30 mins)
      7,748

    Sgp
    Newest Member
    Sgp
    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

    • Scott Adams
      You've done an excellent job of meticulously tracking the rash's unpredictable behavior, from its symmetrical spread and stubborn scabbing to the potential triggers you've identified, like the asthma medication and dietary changes. It's particularly telling that the rash seems to flare with wheat consumption, even though your initial blood test was negative—as you've noted, being off wheat before a test can sometimes lead to a false negative, and your description of the other symptoms—joint pain, brain fog, stomach issues—is very compelling. The symmetry of the rash is a crucial detail that often points toward an internal cause, such as an autoimmune response or a systemic reaction, rather than just an external irritant like a plant or mites. I hope your doctor tomorrow takes the time to listen carefully to all of this evidence you've gathered and works with you to find some real answers and effective relief. Don't be discouraged if the rash fluctuates; your detailed history is the most valuable tool you have for getting an accurate diagnosis.
    • Scott Adams
      In this case the beer is excellent, but for those who are super sensitive it is likely better to go the full gluten-free beer route. Lakefront Brewery (another sponsor!) has good gluten-free beer made without any gluten ingredients.
    • trents
      Welcome to the forum, @catsrlife! Celiac disease can be diagnosed without committing to a full-blown "gluten challenge" if you get a skin biopsy done during an active outbreak of dermatitis herpetiformis, assuming that is what is causing the rash. There is no other known cause for dermatitis herpetiformis so it is definitive for celiac disease. You would need to find a dermatologist who is familiar with doing the biopsy correctly, however. The samples need to be taken next to the pustules, not on them . . . a mistake many dermatologists make when biopsying for dermatitis herpetiformis. 
    • trents
      You state in an earlier post that you don't have celiac disease. Here in this post you state you will "be doing another test". What will this test be looking for? What kind of celiac disease testing have you had done? If you have used a Entero Labs it sounds like you have had stool testing done for celiac disease which is not widely accepted as a valid celiac disease diagnostic testing method. Have you had blood antibody testing for celiac disease done and do you realize that for antibody testing to be valid you must have been eating generous amounts of gluten for a period of weeks/months? 
    • Gigi2025
      No, I've not been diagnosed as celiac.  Despite Entero Labs being relocated to Switzerland/Greece, I'll be doing another test. After eating wheat products in Greece for 4 weeks, there wasn't any reaction.  However, avoiding it here in the states.   Thanks everyone for your responses.  
×
×
  • 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.