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

Gingivitis Or Food Reaction?


LuvMoosic4life

Recommended Posts

LuvMoosic4life Collaborator

I've posted about this before but couldnt find the thread.

I've ben getting little red dots in my mouth off and on. They arent painful, but not very pretty looking. The last time I posted about this I really didn't know what they were (and still dont) but it seems I get them when I am stressed or introducing new foods. They are ussually on the inside of my cheeks and I will only get one or rwo at a time....ysterday I opened my mouth and there was one right near my lip on the inside of my cheek. I've never had one this close to my lips before.....this morning when I woke up I tasted blood and noticed that the little red dot had burst.....its almost like it is a collection of blood that forms......this would explain why I sometimes taste blood for no reason in my mouth.....now I am wondering if these things are forming down my throat b/c I specifically have tasted blood a few times after singing ( I hope they are not on m vocal chords)

but anyways. I take good care of my teeth, floss rinse and brush 2-3 times a day. I havent been able to afford a dentist visit in over year, but decided to make one, I'm going next week. I've also noticed the gums receeding on two of my teeth (the same ones on both sides of my mouth) and it is very snesitive to cold and sugary stuff.... other than that my mouth is healthy....so I dunno

has anyone experienced this? is it a reaction to something I'm doing? or a gum disease? I would find it hard to believe I have a gum disease...but then who knows.....I never knew my whole life that I was gluten intolerant!! I really hope it isnt something more serious....


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



Celiac.com Sponsor (A8-M):



jewi0008 Contributor

Yes, I get these, too!!!!! Mine, I know, though are NOT FROM WHEAT/GLUTEN. I think they may be from nuts or peanuts??? Any thoughts on that? They are definitely food related. They popped up on Thanksgiving again.

If anyone could help us on this it would be so appreciated!

LuvMoosic4life Collaborator

you know. everytime I eat nuts I start feeling like crap and noticed these pop up! It sucks b/c I love nutts.....I'm going off of them for a week or so to see if I feel better.

jewi0008 Contributor

Let me know what happens!!!! My mouth gets REALLY funny...not just the blood things. And I have terrible bm's!!!

you know. everytime I eat nuts I start feeling like crap and noticed these pop up! It sucks b/c I love nutts.....I'm going off of them for a week or so to see if I feel better.
LuvMoosic4life Collaborator

I'll definitly post back after my appt..... hopefully the dentist gives me a better explanation than the school health center (they just said, "oh, thats wierd")

jewi0008 Contributor

have you gone to the dentist yet?!

I'll definitly post back after my appt..... hopefully the dentist gives me a better explanation than the school health center (they just said, "oh, thats wierd")
  • 1 month later...
LuvMoosic4life Collaborator

I believe i finally figured this out.

Salt.

I normally eat all whole foods with very little sodium in my diet. I bought some corn tortillas the other day, i defintly ate too many because I could feel the salt irritating my mouth. I woke up the next day tasting blood in my throat, looked in, sure enough, thre were a few little red dots that have started to burst. It seems to happen whenever I have proccessed crunchy foods, especially corn. I'm going back to completley ignoring corn, I had over 8 trips to the bathroom with D today thanks to tortilla chips. Not sure which ones they were b/c I tried two kinds, Riceworks (which have corn in them) and Santitias...which I know could possibly be CC, but the D reaction happened after the Riceworks chips which I ate yesterday....I havent had corn in so long, so I guess I got my definit answer that I cant tolerat large amounts, if any at all.....I'll try again in the future...with a small amount :lol: ....


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor
I believe i finally figured this out.

Salt.

I normally eat all whole foods with very little sodium in my diet. I bought some corn tortillas the other day, i defintly ate too many because I could feel the salt irritating my mouth. I woke up the next day tasting blood in my throat, looked in, sure enough, thre were a few little red dots that have started to burst. It seems to happen whenever I have proccessed crunchy foods, especially corn. I'm going back to completley ignoring corn, I had over 8 trips to the bathroom with D today thanks to tortilla chips. Not sure which ones they were b/c I tried two kinds, Riceworks (which have corn in them) and Santitias...which I know could possibly be CC, but the D reaction happened after the Riceworks chips which I ate yesterday....I havent had corn in so long, so I guess I got my definit answer that I cant tolerat large amounts, if any at all.....I'll try again in the future...with a small amount :lol: ....

Those little red dots could also have been caused by CC and not by salt. Gluten can and does effect the oral mucosa. There are other countries where they use the mucous membranes of the mouth or the rectum for challenge and diagnosis so that folks don't have to be made ill for months on a food challenge. You also have to keep in mind that the D that results from CC could take as long as 3 or 4 days to hit. I am not saying you don't have an issue with corn, you may. But the best way to challenge that is going to be to leave it out of your diet completely for a bit and then consume it in as 'pure' a form as possible for at least a week and look for a reaction.

Lovey25 Rookie

I know I read somewhere that Celiac/gluten allergy can cause oral ulcers. I have problems with this too and have for a very long time -- on the back of the tongue -- and once I read that info., all of my gluten symptoms started to make more and more sense. After being gluten-free for two and a half months, the ulcers have gotten much better and smaller, though not completely gone.

So maybe even if they're caused by gluten and you've been gluten-free for a while now, perhaps your bleeding ulcers could still just be due to how long you had been eating gluten in your life, before knowing you had a problem. Does that make sense?

I'm not saying I'm right or I'm the expert... it's just an idea that I wanted to throw out there because I know I have problems with it too.

AliB Enthusiast

The red dots are blood blisters. I have had them occasionally - usually near my tonsils at the back of my mouth and usually in response to eating plums of all things (which I now usually avoid unless cooked), but then I have had allergic reactions to peaches and nectarines and occasionally apples and strawberries and they are the same family (rosacea - apples, apricots, cherries, nectarines, peaches, pears, plums and strawberries) so its not surprising really. They all contain malic acid, citric acid and L-quinic acid in different quantities which may be why I react to some fruit but not others. I have reacted occasionally to certain types of apples yet I can eat other types normally with no problem at all. Weird.

People who react to the rosacea family usually have a birch pollen allergy but I am not aware of ever having had that. I can eat them all cooked with no problem at all. People of Mediterranean extraction who have a reaction cannot usually even eat them cooked. Even weirder.

I have wondered if it could be the fruit throwing the acid/alkaline balance in the body out - or even that if our bodies are already over acid the fruit can just tip the balance and that could set up the allergy/reaction.

Blood blisters are due to a food reaction of some kind. There is a possibility in your case it could even be caused by something the food is sprayed with or depending on what it is that is causing the reaction even an additive of some kind.

It may have been the salt, it may have been something that was added to the salt or it may also have been something in the tortilla ingredients. A lot do react to corn and although you may find you can get away with a few chips, perhaps it was the fact that you had too many that triggered the reaction and overloaded your body's ability to cope with whatever it was.

It could be CC from gluten but we can't always assume that to be the case. Many react to a lot more than just gluten.

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. - xxnonamexx replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      My journey is it gluten or fiber?

    2. - cristiana replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    3. - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

    4. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      My journey is it gluten or fiber?

    5. - trents replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

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

    • Total Members
      132,696
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • xxnonamexx
      I read that as well but I saw the Certified Gluten free symbol that is the reason I ourchased it.
    • cristiana
      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac.  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
    • knitty kitty
      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
×
×
  • 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.