Jump to content
  • 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):

Symptoms and my trigger for gluten exposure? Does anyone have this too ?


Tony G

Recommended Posts

Tony G Rookie

Hello, I was diagnosed w celiac in 2016 and I am male age 46- there is some extended family also w celiac.  What happened w me is that I started to get canker sores/ mouth sores in my mouth and especially on tongue and in and around cheeks, inside lip area, they became too frequent and lasted a few days always- would go away for a week and then boom another round of them in my mouth.  After a few visits to different doctors they finally focused on celiac potentially after my blood test showed elevated and then I got a endoscopy to confirm.  Since then I have been very careful w gluten free, I only buy gluten free products at home and don't only go by ingredients labels to see if any wheat, I am sure that occasionally when I do eat out despite being as careful as I can there is inevitably CC ...... I will still get the mouth sores occasionally and it's very hard to determine if they come about bc I have gotten CC or is this something I will always get because I have celiac and doesn't matter if I get exposed to gluten or not??  I am hoping someone else has these type of triggers out there, I don't see this symptom mentioned a lot out there 


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



Celiac.com Sponsor (A8-M):



trents Grand Master

There is a question in my mind as to whether the canker sores are actually caused by your celiac disease. Sounds like the doctors pinned it on celiac disease as there was laboratory evidence proving you were a Celiac. And having canker sores is in fact one of the documented medical conditions associated with celiac disease. But there are many other possible causes.

Have you had follow up lab work and endoscopy to check the response of your celiac disease to gluten free eating?

ravenwoodglass Mentor

Have your doctors done any vitamin and mineral panels on you? Sores like that can be caused by vitamin deficencies. The B vitamins in particular.  You could try supplementing with a stress level B + C combo.

Ennis-TX Grand Master

I second the supplementing, celiac leads to damaged intestines and malabsorbtion of nutrients leading to issues with vitamin deficiencies. One other thought keep a food diary, it could also be caused by another food, spice, or additive in said foods. Celiac messes with your immune system and often we develop allergies and food intolerance issues the longer we leave it untreated. It seems from patterns I noticed that many people get issues with food they were eating when a exposure happened, a theory goes your immune system gets confused and associate another food with the exposure thus developing a allergy or intolerance to it. Other common issues are the fact 10% celiac also react to oats the same. AND due to villi damage many also have issues with producing the enzymes to break down dairy, but I doubt this would lead to your sores.

I get blood blisters/sores in my mouth from corn since I developed a allergy to it. Just a thought the sores could be an allergic reaction to another ingredient. SO keep a food diary and see if you can find a spice, sauce, or ingredient that is associated with these sores your getting.

cyclinglady Grand Master

Just enter “canker sores” in the forum’s search box located at the top right and you will see how many members struggle with canker sores....TONS!  

Tony G Rookie

thank you very much for the replies, at my 6month follow up my labs showed still mildy elevated blood test for celiac and doctor said to be careful with CC but also i had D vitamin deficiency and was low - i did a weekly high dose of vitamin D supplement for about 8 weeks and then they suggested i continue to do an over the counter supplement of Vitamin D supplement (cholecalciferol 1,000 units/daily) which i have been taking the Centrum daily gummies which it says it has extra Vitamin D3 1,000 IU ....is this the same thing or should I be taking something else ?  I am going to be going in soon for another follow up and labs and discuss these things.

As far as diet , yeah its tough to pinpoint....typically i drink coffee, for meals lunch I do have alot of tomato based foods like tomato soup for lunch and then when i do gluten-free Pasta with regular store bottled sauce that says gluten-free and i still have ketchup often with a hamburger at home.  i do alot of chicken dishes with basic seasonings or marinades whcih again are gluten-free

trents Grand Master
3 hours ago, Ennis_TX said:

I second the supplementing, celiac leads to damaged intestines and malabsorbtion of nutrients leading to issues with vitamin deficiencies. One other thought keep a food diary, it could also be caused by another food, spice, or additive in said foods. Celiac messes with your immune system and often we develop allergies and food intolerance issues the longer we leave it untreated. It seems from patterns I noticed that many people get issues with food they were eating when a exposure happened, a theory goes your immune system gets confused and associate another food with the exposure thus developing a allergy or intolerance to it. Other common issues are the fact 10% celiac also react to oats the same. AND due to villi damage many also have issues with producing the enzymes to break down dairy, but I doubt this would lead to your sores.

I get blood blisters/sores in my mouth from corn since I developed a allergy to it. Just a thought the sores could be an allergic reaction to another ingredient. SO keep a food diary and see if you can find a spice, sauce, or ingredient that is associated with these sores your getting.

Do you have references that support this assertion? Oats producing a Celiac reaction has always been a controversial topic, anecdotally, anyway. But as far as I know all the studies done have not supported this when cross contamination with wheat is ruled out. Here is an example from a pretty recent study: Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master
25 minutes ago, trents said:

Do you have references that support this assertion? Oats producing a Celiac reaction has always been a controversial topic, anecdotally, anyway. But as far as I know all the studies done have not supported this when cross contamination with wheat is ruled out. Here is an example from a pretty recent study: Open Original Shared Link

Open Original Shared Link
 

One study, found a few others talking about people with celiac developing a separate antibody reaction to oat proteins, and only certain varieties of oats at that that was done in Europe, I found countless threads of others reacting. I recall reading the 10% ratio years ago but can not find the article, hell even several others and even moderators here quote that statistic. Perhaps they have the study with that saved.....I know I had reactions to oats...it was different then my standard gluten reactions but still caused issues.

trents Grand Master

That article cites a pretty dated study. Doesn't necessarily make it invalid but does make me a little cautious about buying into the premise.

Posterboy Mentor
4 hours ago, trents said:

That article cites a pretty dated study. Doesn't necessarily make it invalid but does make me a little cautious about buying into the premise.

trents and Tony G,

see the canadian site that lists many updated resources.

it is rare but does happen (oats sensitivity) in a small number celiac's.  I didnt' see what percent that was though.

Open Original Shared Link

the gluten free society summarizes the "oats" issue well.

Open Original Shared Link

quoting

"The studies above were all published after Jan. of 2011.  In medicine, it can take 20-30 years for new information to become common knowledge among doctors.  So I don’t expect that many physicians will be talking about the potential for oat to be a problem for those with gluten sensitivity."

and they term it a "subgroup"

as often is the case many times we as patients often know our bodies better than the doctor's do.

Tony G as for the mouth uclers.

swilling with salt water will help them go away quicker.

but taking the amino acid Lysine will help your ulcers/caneker sours stay in remission. 

take it 1000mg at a time with each meal and 3 or 4 days they will mostly go away especially if you use the salt water method with the lysine.

you can take lysine ahead of an outbreak too to keep them at bay.

***this is not medical advice but I hope it is helpful. I only know it helped me.

I used to take Lysine but don't need it much anymore these days.

your arginine/lysine balance is out of wack.  You can google it.

oh . . the red sauce (tomatoes) you described is exactly what caused my mouth to be sore/raw right before an out brake.  I usually could take them for a a week until they went away on their own unless they got on my tongue and then only eating one side was more than I could bare and out would come the lysine and salt water. . .  Until I learned to take it (lysine) to keep them at bay and my lysine/arginine ratios  in balance.

again I hope this is helpful.

posterboy,

trents Grand Master

Good point, Posterboy about the lag time between research and findings becoming common knowledge in the medical community.

GFinDC Veteran

Hi TonyG,

Check out the info at the vitamin D council site.  They ran tests on various vitamin D pills.  They are not all the same.  Also, oily fish is a good natural source of vitamin D.

Open Original Shared Link

 

AJS3849 Rookie

Another possibility for the mouth sores would be GERD.  Celiac and GERD often go hand-in-hand.  There is a mistaken belief that heartburn is the most common manifestation of GERD, but that is not necessarily so.  It is possible to have "silent reflux" or "respiratory reflux" where the acid actually invades your mouth and sinuses and this can cause mouth sores.  An excellent book on the subject is "Dr. Koufman's Acid Reflux Diet" by Dr. Jamie Koufman.  It was recommended to me by the nutritionist at my gastroenterologist's office and I've found it very helpful in explaining symptoms that were difficult to diagnose and in offering dietary modifications that I have found far more effective than medications.

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. - Aretaeus Cappadocia replied to nancydrewandtheceliacclue's topic in Super Sensitive People
      11

      Celiac flare years after diagnosis

    2. - Aretaeus Cappadocia replied to nancydrewandtheceliacclue's topic in Super Sensitive People
      11

      Celiac flare years after diagnosis

    3. - Peace lily commented on Scott Adams's article in Latest Research
      2

      New Study Reveals How the Immune System Learns Which Foods Are Safe to Eat

    4. - nancydrewandtheceliacclue replied to nancydrewandtheceliacclue's topic in Super Sensitive People
      11

      Celiac flare years after diagnosis

    5. - Jmartes71 replied to Jmartes71's topic in Dermatitis Herpetiformis
      4

      Skin issues

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

    • Total Members
      134,061
    • Most Online (within 30 mins)
      10,442

    Francisco1007
    Newest Member
    Francisco1007
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.7k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Aretaeus Cappadocia
      @nancydrewandtheceliacclue, you are welcome. After looking at this thread again, I would like to suggest that some of the other comments from @Russ H are worth following up on. The bird-bread may or may not be contributing to what you are experiencing, but it seems unlikely to be the whole story. If you have access to decent healthcare, I would write down your experiences and questions in outline form and bring this to your Dr. I suggest writing it down so you don't get distracted from telling the Dr everything you want to say while you have their attention.
    • Aretaeus Cappadocia
      @Russ H, I partly agree and partly disagree with you. After looking at it again, I would say that the slick graphic I posted overestimates the risk. Your math is solid, although I find estimates of gluten in white bread at 10-12% rather than the 8% you use. Somewhat contradicting what I wrote before, I agree with you that it would be difficult to ingest 10 mg from flinging bread.  However, I would still suggest that @nancydrewandtheceliacclue take precautions against exposure in this activity. I'm not an expert, I could easily be wrong, but if someone is experiencing symptoms and has a known exposure route, it's possible that they are susceptible to less than 10 mg / day, or it is possible that there is/are other undetected sources of exposure that together with this one are causing problems. At any rate, I would want to eliminate any exposure until symptoms are under control before I started testing the safety of potentially risky activities. Here is another representation of what 10 mg of bread would look like. https://www.glutenfreewatchdog.org/news/wp-content/uploads/2019/10/10mgGlutenCrumbsJules.jpg Full article that image came from: https://www.glutenfreewatchdog.org/news/what-does-10-mg-of-gluten-look-like/
    • nancydrewandtheceliacclue
      @Aretaeus Cappadocia thank you for your reply and the link, that is very helpful to get a visual of just how small of an amount can cause a reaction. I know I am not consuming gluten or coming into contact with gluten from any other source. I will stop touching/tossing bread outside! My diet has not changed, and I do not have reactions to the things I am currently eating, which are few in number. My auto immune reaction just seems so severe. The abdominal pain is extreme. It takes a lot out of me. I guess I will be this way for the rest of my life if I ever happen to come into contact with gluten? I appreciate the help. 
    • Jmartes71
      Thankyou I did find out the Infectious disease is the route to go rather than dermatologist. I did reach out to two major hospitals and currently waiting on approval for one of them in Infectious Diseases to call me. I also did have implants ( I didn't know and sense not properly in my medical. Neither did surgeon)in 2006 and there was a leak 2023 during the same time I was dealing with covid, digestive issues, eyes and skin.Considering I " should  be fine" not consuming gluten/wheat, taking vitamins for sibo and STILL feeling terrible.It has to be parasites. I also take individual eye drops prescribed, could there be an issue there? Anyways my pcp thinks I need therapy because again they don't acknowledge my digestive issues because in my records it shows im fine, hintz the reason I had to go back to bay area hospital:(  I thought skin issues maybe sibo related but I feel and have seen and seriously trying not to think about it because it's disgusting. 
    • Aretaeus Cappadocia
      oops. I didn't see that before posting or I would have at least referenced it. The two recipes are pretty similar, but I think the newer one is a little simpler/faster. Next time though I will search more before posting.
×
×
  • Create New...