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

11 Cavities In A 3 Year Old?


floridanative

Recommended Posts

floridanative Community Regular

Okay - some of you know that I have tried unsuccessfully to get my sister (tested neg. for Celiac) to get her children tested as well. The girl catches every virus around and is sick 1/2 the time and the boy who is three is thought to have lactose intolerance which you know Celiac imitates very well. So we were visiting the family out of town over the weekend and my husband informed me that my nephew has 11 cavities according to my sister. Does this sound abnormal to anyone or is that just the way some kids baby teeth are? He does not eat a lot of sugar and if he gets a soda it's a very rare treat - unlike most other kids I know who drink soda every day and do not have cavities. As I the aunt and my Mother (the kids blood grandmother) both have Celiac, we know it runs in the family. I have two cavities now and had a root canal last spring and just now found out I have osteopenia due to lack of calcium absorption. I'd appreciate any opinions I can get.


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

I have six kids and none of them had anywhere near 11 cavities by the time they were three!!!! Not normal!

AndreaB Contributor

If the child ate a lot of candy, sweets, pop, sugar, sugar, sugar, then I would say yes.

Also if the child never brushed their teeth I'd say maybe.

Something else is going on here (IMO)

nikki-uk Enthusiast

Sounds very similar to my friends little boy.

By the age of around 6yrs he had to have 5 teeth out as the dentist couldn't save them-in fact,it was the dentist who suggested that he wasn't absorbing calcium.

After seeing a paediatrician,he thought it was celiac disease,but bloods were negative.He was eventually diagnosed with lactose intolerance.

I've gotta say,I do actually wonder though-is he a coeliac?

My friend thinks I am a crazy coeliac spotter( :ph34r: !),but I know that he still has D even when he hasn't had milk,but hey I've broached the subject,and she's happy with the fact that he had neg bloods all them years ago <_<

Have you explained to your sister that the state his teeth could be due to celiac disease?

At the end of the day,if she's adamant you're wrong about celiac disease,there's not much else you can do-although very frustrating I know. :)

jerseyangel Proficient

That sounds like an excessive amount of tooth decay for a 3 year old--especially one who eats very little sugar. Considering the family history, this added with the lactose intolerance should convince your sister to have him tested. What does she have against the testing?

floridanative Community Regular

First of all - thank you to everyone for sharing your opinions.

Jerseyangel - you may not have read my older post about my sister's idiot pediatrician. He thinks if my sister doesn't have Celiac - her kids do not need to be tested. I've sent all the proven medical info showing that is ridiculous and told her repeatedly her kids should be tested at age five even if they have NO symptoms due to our family history. I guess she doesn't want him to have it and really the baby teeth will fall out eventually. But if he gets cavities in his permanent teeth like he has now, I don't think my sister can put off testing him for Celiac then. I just think it would be better to find out now if he has it since he could go off gluten and he'd never even remember having it.

jerseyangel Proficient
First of all - thank you to everyone for sharing your opinions.

Jerseyangel - you may not have read my older post about my sister's idiot pediatrician. He thinks if my sister doesn't have Celiac - her kids do not need to be tested. I've sent all the proven medical info showing that is ridiculous and told her repeatedly her kids should be tested at age five even if they have NO symptoms due to our family history. I guess she doesn't want him to have it and really the baby teeth will fall out eventually. But if he gets cavities in his permanent teeth like he has now, I don't think my sister can put off testing him for Celiac then. I just think it would be better to find out now if he has it since he could go off gluten and he'd never even remember having it.

Hi Tiffany--Yes, I missed that post. The doctor--should have known <_< I just hate to see anyone have a delay in diagnosis. I hope that she will change her mind--it would be easier for the little boy to get off gluten now, if need be, before he gets any older. Not to mention his health and development if he does have it.


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor
First of all - thank you to everyone for sharing your opinions.

Jerseyangel - you may not have read my older post about my sister's idiot pediatrician. He thinks if my sister doesn't have Celiac - her kids do not need to be tested. I've sent all the proven medical info showing that is ridiculous and told her repeatedly her kids should be tested at age five even if they have NO symptoms due to our family history. I guess she doesn't want him to have it and really the baby teeth will fall out eventually. But if he gets cavities in his permanent teeth like he has now, I don't think my sister can put off testing him for Celiac then. I just think it would be better to find out now if he has it since he could go off gluten and he'd never even remember having it.

Please let her know that even though these are baby teeth the adult ones are also being effected. How is his growth, ask her where he was at birth and where he is now. Has he lost ground? Undiagnosed celiac in children has life long effects to their brains and bodies. It can stunt growth severely and can cause problems with learning and cognition. The longer she waits the more chance there is that the delay will cause permanent damage. I hope she not only will test but will also try the diet.

flagbabyds Collaborator
Okay - some of you know that I have tried unsuccessfully to get my sister (tested neg. for Celiac) to get her children tested as well. The girl catches every virus around and is sick 1/2 the time and the boy who is three is thought to have lactose intolerance which you know Celiac imitates very well. So we were visiting the family out of town over the weekend and my husband informed me that my nephew has 11 cavities according to my sister. Does this sound abnormal to anyone or is that just the way some kids baby teeth are? He does not eat a lot of sugar and if he gets a soda it's a very rare treat - unlike most other kids I know who drink soda every day and do not have cavities. As I the aunt and my Mother (the kids blood grandmother) both have Celiac, we know it runs in the family. I have two cavities now and had a root canal last spring and just now found out I have osteopenia due to lack of calcium absorption. I'd appreciate any opinions I can get.

Thats weird!

I've never had a cavatie, and im 16.

You gotta love them rich silicon valley people having flourine in the h2o we drink out of the tap.

TCA Contributor

My son is 3 and had dentla surgery week before last for his nonexistant enamel. 7 crowns, 3 fillings, and sealants on the 2 teeth that were left. He had classic sypmtoms since birth and had a dairy allergy that he outgrew. His bloodwork was inconclusive and he had 2 neg. biopsies. Symptoms persisted, so we tried the diet and it was a miraculous turn around. After gene testing, he was given a somewhat positive diagnosis. Not on his chart, but to me because of insurance purposes. The dr. knows me well and said he didn't want to do more harm than good since he knows I"ll keep him on the diet.

Please tell these moms to try the diet even if the tests are negative. I guess that is if you can get them to do the tests in the first place!!!

My SIL needs to be tested too, but hasn't been. I think she just doesn't want to know. It's frustrating, but we can't make thier decisions for them.

prinsessa Contributor

I had tons of cavites my whole life (starting at a young age) and I never ate much candy and brushed my teeth all the time. I never had symptoms of gluten intolerance before a year or so ago so I don't know if that has anything to do with it (I think it does though). Hopefully your sister will get him tested. Good luck!

gfp Enthusiast

floridanative: Is this in the UK? just asking because the dental service is terrible and the way dentists get paid is by creating work.

When I was about 10 my dentist retired and someone took over the practice. I went from no cavities to him finding a new one each time, I stopped going when I was 11-12 but my mother continued and eventually ended up in a malpractice suite .. long story... and although the dental assoc defended his actions offically he was struck off for something else about a year after.,

chrissy Collaborator

some kids just have really soft baby teeth(2 of my non-celiacs have had to have some pulpotomies on baby teeth, but with celiac in the family i would sure want to get them tested if i were your sister------is she not testing because her doc doesn't feel it is necessary, or because she just doesn't want to do it?

floridanative Community Regular

Where my sister lives, there is not ONE doctor in the entire town who knows any current info on Celiac. My onw Celiac Mother is supposed to have a biopsy late this month when she'll have been gluten free for over three months.....at least the diet is working for her so I don't think she'll go back to gluten when he tells her she doesn't have Celiac - blookwork was positive in March.

Back to my sister's ped. He knows almost nothing of Celiac (dx'd his first patient with it recently and he's in his 40's) and told her if she doesn't have it then there's no need to test her kids. It's hard to convince people that doctors really don't know about Celiac and my sister knows I haven't been to medical school.... I've sent her all the info with all the symptoms and I just think she doesn't want her kid to have it so she'd rather not think that he could. I've been fairly abnoxious about the fact that her doc knows nothing, can't be trusted to recognize Celiac, and her kids both need to be tested. Now I have to tread lightly so I can keep a relationship with my sister. We only see each other a few times a year but I don't want those times to be strained because of the Celiac elephant in the room.

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. - TheDHhurts posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      need help understanding testing result for Naked Nutrition Creatine please

    2. - cristiana replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      14

      Insomnia help

    3. - wellthatsfun posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      nothing has changed

    4. - trents replied to Charlie1946's topic in Related Issues & Disorders
      48

      Severe severe mouth pain

    5. - Charlie1946 replied to Charlie1946's topic in Related Issues & Disorders
      48

      Severe severe mouth pain

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

    • Total Members
      133,105
    • Most Online (within 30 mins)
      7,748

    kyocera
    Newest Member
    kyocera
    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

    • TheDHhurts
      Hi, I bought Naked Nutrition Creatine. It lists itself as gluten free but is not certified. (It used to be, but they dropped it in the past year or two apparently.) I wrote the company and asked them what testing results they had for creatine and they sent me the attached, which says the test result for gluten is <0.025MCG. I'm used to seeing test results as ppm, so I'm not sure what <0.025MCG means. Can it be converted to ppm easily? I want to confirm that it is safe to use.
    • cristiana
      When I was still recovering my gastroenterologist suggested I bought lactofree product as I was very bloated.  So I bought some from the supermarket and from memory, I drank a nice big glass of milk - and it went right through me literally within an hour or so, if my memory serves correctly.  I came off dairy completely next and it worked like a charm, but started to reintroduce quite gradually it as I missed it! To this day, if I overdo dairy products, they work like a mild laxative.  I've never wanted to give up milk completely as I like it so much, and my mum had osteoporosis and it's an easy way of getting calcium.  But it doesn't really 'sit' well with me.   You may need to experiment a bit as when I was healing certain dairy products were worse than others - I could cope with one brand of Greek yoghurt, but I got extremely and painfully bloated with another brand of live British yoghurt.  
    • wellthatsfun
      i have been strictly gluten free for 7 months. this includes avoiding anything that may contain gluten and making sure surfaces and appliances are clean. i am 18 years old in australia and my tTG-IgA results were 69U/mL, pretty low compared to most people's, for reference. i feel the exact same as before. sure, i was pretty much asymptomatic/silent. the worst i'd get was occasionally bad stools and pitting of the nails/brittle hair since early childhood - and i was diagnosed with low iron and vitamin d which checks out due to easy bruising and such. but those symptoms have remained. maybe i'm jumping the gun, sure. i know it can take years to fully heal. but being over half a year in, i feel that i should be, y'know, healing. i'm nearly at my wits end and wondering if i should have a piece of bread or something to see how i go - to see if i possibly have refractory? my mental health is declining as i feel myself wanting to bang my head against a damn wall out of frustration every day. cravings haven't gotten better. look, i love the stuff i still can have, like salads and such. OH! i haven't lost any weight, which is mind boggling considering i eat very healthily now! i've always been on the chubbier side which is atypical of coeliac. i just don't know what's going on with me. i try to remain hopeful but i'm just so sad all the time. thanks for reading  
    • trents
      @Charlie1946There is a PM (Personal Message) tool built into the forum website that allows you to send a private message to other forum users. Just hover over their name with your mouse cursor and the menu containing that tool will pop up. This is useful if you want to communicate with an individual without everyone else involved in the thread seeing it.  Are you realizing that in my PPI taper down recommendations in an earlier post above, I was responding not to your posts but to @Caligirl57? If you must use a PPI, I certainly would advise taking the lowest dose that is effective for you.  
    • Charlie1946
      Hi everyone, I'm still trying to figure out how to each message individually. I saw one with some information on sebaceous hyperplasia but now I can't find it. I appreciate you all so much for all your responses and advice! God bless! Hi everyone, I'm still trying to figure out how to each message individually. I saw one with some information on sebaceous hyperplasia but now I can't find it. I appreciate you all so much for all your responses and advice! God bless! Hi everyone, I'm still trying to figure out how to each message individually. I saw one with some information on sebaceous hyperplasia but now I can't find it. I appreciate you all so much for all your responses and advice! God bless! Hi everyone, I'm still trying to figure out how to each message individually. I saw one with some information on sebaceous hyperplasia but now I can't find it. I appreciate you all so much for all your responses and advice! God bless! Hi everyone, I'm still trying to figure out how to each message individually. I saw one with some information on sebaceous hyperplasia but now I can't find it. I appreciate you all so much for all your responses and advice! God bless!
×
×
  • 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.