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

Biting Inside Of My Cheeks


mamaloca2

Recommended Posts

mamaloca2 Apprentice

Does anyone kno wif there is a connection between Celiac disease and habitual biting of the inside of the mouth. I have done it since I was a kid and now my son who is only four does it. Does anyone else have this problem?


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



Celiac.com Sponsor (A8-M):



chrissy Collaborator

sounds more like an obsessive-complulsive behavior-----and OCD can run in families.

jennyj Collaborator

Wow. I have done this as long as I can remember. My dad used to say "Jenny stop it," all the time. I tend to do it when I am very nrevous or watching TV. I don't know if there is a connection but you are not alone.

Kellygirl Rookie
Wow. I have done this as long as I can remember. My dad used to say "Jenny stop it," all the time. I tend to do it when I am very nrevous or watching TV. I don't know if there is a connection but you are not alone.

Yep I am obsessive complusive and I do it all the time, even while sleeping. I am celiac too, but I never really questioned if they go together or not!

Kelly

mamaloca2 Apprentice
sounds more like an obsessive-complulsive behavior-----and OCD can run in families.

I don't have any other traits that are OCD. And I only really bite them when a am stressed. I just noticed when I got glutened that I did it much more, and thought there could be a connection.

mamaloca2 Apprentice
Wow. I have done this as long as I can remember. My dad used to say "Jenny stop it," all the time. I tend to do it when I am very nrevous or watching TV. I don't know if there is a connection but you are not alone.

Us too! Even if it's not related to celiac, seems like there's got to be something more to it. Thanks for your reply!

RiceGuy Collaborator

I used to have similar sorts of stuff happen, but by accident. Usually it was my lip that got chomped :angry: Thankfully, this has subsided/disappeared, and I believe the key was a sublingual methylcobalamin (vitamin B12) supplement. Either that or it just took time, but I notice that my teeth are straighter too, and no longer have the aching that would come and go.

Still a bit of teeth clenching, but not as bad as it used to be.


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

I actually trained myself to do this. On gluten or under great stress I am a teeth grinder. I have broken them in my sleep, those good old celiac teeth, and I do it to keep from grinding. Perhaps a mouth guard might help you and your son, your dentist can give you one with the best fit. Another thing that helps, at least for me, is a hot compress on my cheek before bed. When I get glutened it helps my muscles to relax and I don't do as much grinding and biting. Plus it feels very soothing.

cmom Contributor

I used to accidentally bite the inside of my mouth and once I did it, it seemed like I did it several times, each time very painful. Hadn't thought much about it until reading these posts. That's a good thing cause that means it "ain't " happenin' anymore!!!!!!

zakismom Newbie

I used to do this all the time! I also used to bite my lip until it turned into a bump. I don't do it as much but I do know that if I get glutened I get a mouth sore.

Rusla Enthusiast

I do this all the time, although it could be not just an ocd but in some cases a tourettes thing.

Stargirl* Newbie

Hi.

I am a long time lurker, first time poster. ;)

My daughter bites the inside of her cheeks and lips. I have put it down to the mouth ulcers she used to have until the gluten intolerance diagnosis.

  • 4 weeks later...
mwahlman Newbie

You may be refering to TMJ. I was recently diagnosed with this by my dentist, around the same time as my Celiac Diagnosis.

I am unsure if the two are directly related, or if I just have been lucky finding medical professionals who arent qwacks lately.

"TemporoMandibular Joint and muscle disorders" The following article goes over the specifics:

Open Original Shared Link

Does anyone kno wif there is a connection between Celiac disease and habitual biting of the inside of the mouth. I have done it since I was a kid and now my son who is only four does it. Does anyone else have this problem?
lob6796 Contributor
Does anyone kno wif there is a connection between Celiac disease and habitual biting of the inside of the mouth. I have done it since I was a kid and now my son who is only four does it. Does anyone else have this problem?

Interesting, I would have never connected the two. I do it alot (ugh the scars!), and my mom, who never knew she did it, went to a special dentist the other day and the lady goes "wow, you really bite your mouth alot, huh?" The dentist said she is probably doing it in her sleep without realizing it. I have Celiac, and she is suspected of having it.

Guhlia Rising Star

I am mildly OCD and I compulsively scratch my lips with my teeth. I'm assuming this is about the same as what you guys are talking about. Luckily, most of my OCD symptoms disappeared when I went gluten free. Unfortunately, this one hasn't gone away completely. It has gotten better though since going gluten free. I think there's definitely a connection with OCD and gluten.

Ursa Major Collaborator

I have Tourette's syndrome and Asperger Syndrome, and I have always done that, too. It isn't possible to determine if in my case it is a tic, OCD (which I have mildly, but not enough for a separate diagnosis, as EVERYBODY with TS and AS has some compulsive behaviours) or a stim (self-stimulating behaviour, typical for people on the autistic spectrum).

But I do know that I don't do things like that as much as I used to when still eating gluten, and my tics have decreased as well.

JamiD Apprentice

*reluctantly raises hand*

Gawd, I'm doing it right now.

I've habitually chewed/bit my inside cheeks and lips since I was a teen. I do it more when I'm not physically busy.

Never been diagnosed w/ OCD and I would say that if I have it, it is mild.

  • 3 weeks later...
glutenfreek Newbie

Add one more person with celiac and bites their tongue...literally. I have wondered about OCD, never been diagnosed, but that doesn't mean much. Like others have mentioned I remember doing this as a child, my grandmother did it and so does my father. I have tried to stop numerous times, hence why I am on this site right now, seeing if anybody has ever been successful in kicking this nasty habit. I used to grind my teeth too and my dentist made me a mouth guard, (Wal Mart sells a mouth guard that you mold to your teeth at home, fairly easy to do and only $20). This stopped my grinding but I am having trouble with biting my tongue still. It is sooooo irritating, I do it in my sleep and sub consciously. I don't understand why I do this, I absolutely hate it, my tongue is sore all the time and looks repulsive I want to stop! Any suggestions or advice would be appreciated.

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. - knitty kitty replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      6

      Help understand results

    2. - knitty kitty replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      10

      Insomnia help

    3. - trents replied to pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Positive biopsy

    4. - pothosqueen posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Positive biopsy

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

    • Total Members
      132,993
    • Most Online (within 30 mins)
      7,748

    Tchudi
    Newest Member
    Tchudi
    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

    • knitty kitty
      That test is saying that your daughter is not making normal amounts of any IGA antibodies.  She's not making normal amounts of antibodies against gliadin, not against bacteria, not against viruses.  She is deficient in total IGA, so the test for antigliadin antibodies is not valid.  The test was a failure.  The test only works if all different kinds of antibodies were being made.  Your daughter is not making all different kinds of antibodies, so the test results are moot.  Your daughter should have the DGP IgG and TTG IgG tests done.   The tests should be performed while she is still consuming gluten.  Stopping and restarting a gluten containing diet can make her more sick, just like you refuse to eat gluten for testing.  Call the doctor's office, request both the IGG tests. Request to be put on the cancellation list for an appointment sooner.  Ask for genetic testing.   Celiac disease is passed on from parents to children.  You and all seven children should be tested for genes for Celiac disease.  Your parents, your siblings and their children should be tested as well.  Eating gluten is not required for genetic testing because your genes don't change.  Genetic testing is not a diagnosis of Celiac disease.  Just having the genes means there is the potential of developing Celiac disease if the Celiac genes are activated.  Genetic testing helps us decide if the Celiac genes are activated when coupled with physical symptoms, antibody testing, and biopsy examination. It's frustrating when doctors get it wrong and we suffer for it.  Hang in there.  You're a good mom for pursuing this!  
    • knitty kitty
      @hjayne19, So glad you found the information helpful.  I know how difficult my struggle with anxiety has been.  I've been finding things that helped me and sharing that with others makes my journey worthwhile. I like Life Extension Bioactive Complete B Complex.  It contains the easily activated forms of B vitamins needed by people with the MTHFR genetic variation often found with Celiac disease.   Avoid B Complex vitamins if they contain Thiamine Mononitrate if possible.  (Read the ingredients listing.)  Thiamine Mononitrate is the "shelf-stable" form of B 1 that the body can't utilize.  B vitamins breakdown when exposed to heat and light, and over time.  So "shelf-stable" forms won't breakdown sitting on a shelf in a bright store waiting to be bought.  (It's also very cheap.)  Thiamine Mononitrate is so shelf-stable that the body only absorbs about thirty percent of it, and less than that is utilized.  It takes thiamine already in the body to turn Thiamine Mononitrate into an active form.   I take MegaBenfotiamine by Life Extension.  Benfotiamine has been shown to promote intestinal healing, neuropathy, brain function, glycemic control, and athletic performance.   I take TTFD-B1 Max by Maxlife Naturals, Ecological Formulas Allthiamine (TTFD), or Thiamax by EO Nutrition.  Thiamine Tetrahydrofurfuryl Disulfide (TTFD for short) gets into the brain and makes a huge difference with the anxiety and getting the brain off the hamster wheel.  Especially when taken with Magnesium Threonate.   Any form of Thiamine needs Magnesium to make life sustaining enzymes and energy.  I like NeuroMag by Life Extension.  It contains Magnesium Threonate, a form of magnesium that easily crosses the blood brain barrier.  My brain felt like it gave a huge sigh of relief and relaxed when I started taking this and still makes a difference daily.   Other brands of supplements i like are Now Foods, Amazing Formulas, Doctor's Best, Nature's Way, Best Naturals, Thorne, EO Nutrition. Naturewise.  But I do read the ingredients labels all the time just to be sure they are gluten and dairy free. Glad to help with further questions.  
    • trents
      Welcome to the celiac.com community @pothosqueen!   Can you be more specific about which IGA test was run that resulted in 114 score and said to be "normal" and could you please include the reference range for what would be normal? By the size of that number it looks like it may have been what we call "total IGA" but that test is not usually run without also running a TTG-IGA. Total IGA tests for IGA deficiency. If someone is IGA deficient, then the celiac-specific IGA tests like the TTG-IGA will be inaccurate. Was this the only IGA test that was run? To answer, your question, yes, a positive biopsy is normally definitive for celiac disease but there are some other medical conditions, some medications and even some food proteins in rare cases that can cause positive biopsies. But it is pretty unlikely that it is due to anything other than celiac disease.
    • pothosqueen
      Upper endoscopy last week resulted in positive biopsy for celiac disease. The IgA they ran was normal (114). Does positive biopsy automatically mean definitive diagnosis?
    • hjayne19
      This is great thank you very much @Scott Adams
×
×
  • 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.