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

About My 3 Y/o Son


my3yo

Recommended Posts

my3yo Newbie

I have a 3 y/o son who has some strange symptoms and I am wondering if he might be sensitive to gluten and wanted some opinions.  He was tested last fall for only a couple allergies (environmental) and is allergic to dogs, cats, and dust mites...no foods were tested.  I have always limited his dairy because I am lactose intolerant (trying a gluten free diet to see if that is really my problem).  As he's gotten older I've increased his dairy and he seems to tolerate it.  But  he has constant loose stools.  His pediatrician said its not a problem but it is horrible smelling and he farts all the time.  I believed the dr. when she said not to worry about the loose stool but now I have 7 mo old who already has formed stool most of the time and my 3 y/o has never (maybe rarely) had formed stool.  Also, he has a urinary problem I think.  He will sometimes pee every 10-30 minutes all day long.  I've read that gluten can cause damage to the bladder and cause frequency and urgency symptoms.  The doctor checked him for diabetes because of his frequent urination and he does not have an infection.  He also has dry/rashy skin almost always but he has red hair and very fair skin so I just figured he had sensitive skin.  Also I've read that gluten can cause "flabby muscles" and my sister has always told me that his hands seem to have low muscle tone and always seem loose/floppy.  I don't have anything to compare it too.  I think his feet are floppy and he tends to be slightly pidgeon toed and the doctor said that the muscles with improve with age and correct itself.  He was also anemic at 1 year old and takes an iron supplement now.  I don't know, could be a lot of unrelated coincidences and I could just be a crazy mom thinking something more is wrong but I'm just not sure and thought someone here might have more insight.  I thought about just putting him on a gluten free diet for 2 weeks to see if his stool hardens.


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



Celiac.com Sponsor (A8-M):



moosemalibu Collaborator

I don't think you are a 'crazy mom' at all. A lot of the symptoms you are talking about are signalment of celiac disease in children. I would request a celiac panel for him. Be sure he is eating gluten though otherwise it could be a false negative.

nvsmom Community Regular

I too would have him tested before trying the diet because if you want to test later, you'll have to reintroduce gluten for a few weeks for accurate testing- two months if he has been gluten-free for a long while.

When requesting testing, ask for:

TTG IgA and tTG IgG (most popular tests)

DGP IgA and DGP IgG (these are the best tests for kids, by far)

Ema IgA (tends to be positive in more advanced cases)

Total serum IgA (a control test)

AGA IgA and AGA IgG (older and less reliable tests)

The endoscopic biopsy is also an option

Be aware that celiac disease tests are not as reliable for very young children so there is a greater chance for false negatives. False negatives can happen if testing after going gluten-free too.

If your 3yo does have negative results, it old be non-celiac gluten intolerance (NCGI) which has all the same symptoms of celiac disease except for the villi damage. It could also be due to false negatives. If he is negative, try the gluten-free diet anyways but give it a minimum of two months (six is much better) before you decide if it has helped. There are many symptoms that can take months to improve and sometimes BM's are slow to change. Keeping a symptom and food journal will help keep track of the changes.

Good luck!

my3yo Newbie

I talked with my husband and he doesn't see a reason to get our son tested.  He thinks that we should just put him on a gluten free diet and if he gets better that is enough of a reason not to have gluten.  Is there really a need to get tested?  If he is celiac vs. gluten sensitive, the diet is the same.  Is it important for other reasons to have the diagnosis officially?  I'm just wondering because I really don't know what to say to my husband.  Thanks for all your advice so far!  I appreciate it!

frieze Community Regular

if you are in the USA, you will need dx to require school to comply.

nvsmom Community Regular

I agree that the main reason would be for school accommodations. Check with the schools in your area and find out how they would handle food sensitivities with or without a doctor's diagnosis.

snowmom Rookie

Once you eliminate gluten, it's very difficult to test for celiac down the road. As pps said, if it is truly celiac, a formal diagnosis is important for school accommodation. But it could also help ensure that your DS adheres to the diet as he grows up and makes his own food decisions.  We have a relative who decided that her toddler had problems with gluten many years ago (and the child probably did have either NCGI or celiac), but now that he's an almost teenager I don't think he takes it as seriously as he would if he'd been told that he had a disease. I'm not that familiar with how sensitive people with NCGI are to varying levels of gluten, but with celiac, your child must ensure total lifelong gluten elimination, which isn't a walk in the park. Impressing on our DD (and our friends and relatives who eat with her) the gravity of the diagnosis was one of the reasons we wanted biopsy confirmation.

 

One other benefit of getting a formal diagnosis is insurance coverage following diagnosis. That covers follow-up testing to make sure the antibody levels are improving and, depending on your carrier, it might also include dietary counseling as you begin the gluten-free diet. Our GI practice also  screens celiac kids for other associated autoimmune diseases, although I'm not sure if all GIs do that.


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



Celiac.com Sponsor (A8-M):



greenbeanie Enthusiast

I would also recommend getting him tested. Though a blood draw is no fun with a little kid, if the results give any indication of celiac it could turn out to be really important later to have proper follow-up covered by insurance.

As for the urinary frequency issue, my daughter and I both had that. We'd both have to pee several times an hour, all day long. For me this went on for over 20 years, and like your son I was checked for diabetes and infections (many times) and always had normal results. My daughter had traces of blood in her urine several times, with no infection, and doctors could never figure out why. She was diagnosed with celiac last summer, just after she turned four, and I had a confusing mix of test results but went strictly gluten-free along with her. The urinary frequency stopped for both of us within a week, and it hasn't returned.

my3yo Newbie

Thanks so much for all your help so far!  I talked with my husband again and am planning to make an appointment with the pediatrician in the next few weeks to talk to her about this.  I have a feeling we will be referred to a GI specialist if she thinks I'm on to something and I don't know how long that will take.  Other than the tests mentioned above is there anything specific I should request, ask or mention symptom wise to her.  I'm going to try to write everything out so I don't forget stuff.  

my3yo Newbie

I would also recommend getting him tested. Though a blood draw is no fun with a little kid, if the results give any indication of celiac it could turn out to be really important later to have proper follow-up covered by insurance.

As for the urinary frequency issue, my daughter and I both had that. We'd both have to pee several times an hour, all day long. For me this went on for over 20 years, and like your son I was checked for diabetes and infections (many times) and always had normal results. My daughter had traces of blood in her urine several times, with no infection, and doctors could never figure out why. She was diagnosed with celiac last summer, just after she turned four, and I had a confusing mix of test results but went strictly gluten-free along with her. The urinary frequency stopped for both of us within a week, and it hasn't returned.

 

Thank you for mentioning the urine frequency symptoms.  My husband thinks he is just waiting too long to go to the bathroom (and I agree with this at times) but there is no reason he should have to go to the bathroom that often.  We already limit his fluids per the pediatrician as that was all she recommended we do when he was negative for diabetes.  Today he went to the bathroom at least every half hour and leaked into 3 pairs of underwear.  Maybe this is his issue.  The only thing that doesn't make sense is sometimes he doesn't seem to have the frequency.  Sometimes he'll go a week and do well and hold his urine for 3-4 hours...maybe he has less gluten during these times?

snowmom Rookie

my3yo, I'm talking way out of my expertise here, but on the urinary frequency issue, you might check out these two articles. Some very reputable doctors have speculated that there's an association between constipation and bedwetting and wetting accidents: 

 

Open Original Shared Link

 

Open Original Shared Link

 

Of course, in some kids, constipation could also be a symptom of celiac or gluten intolerance, so this could all be part of a larger picture. But either way, it seems like your doc should be trying to get to the bottom of the urinary frequency issue, and not just tell you to limit his fluids (that advice sounds kind of unusual to me).  Hopefully a GI can look at all of these symptoms and help you find an answer!! Best wishes.

my3yo Newbie

my3yo, I'm talking way out of my expertise here, but on the urinary frequency issue, you might check out these two articles. Some very reputable doctors have speculated that there's an association between constipation and bedwetting and wetting accidents: 

 

Open Original Shared Link

 

Open Original Shared Link

 

Of course, in some kids, constipation could also be a symptom of celiac or gluten intolerance, so this could all be part of a larger picture. But either way, it seems like your doc should be trying to get to the bottom of the urinary frequency issue, and not just tell you to limit his fluids (that advice sounds kind of unusual to me).  Hopefully a GI can look at all of these symptoms and help you find an answer!! Best wishes.

 

Thanks for the articles.  I found them very interesting.  I think I'm going to just have to talk with his pediatrician about everything.  I wouldn't guess he is constipated as he usually has a bowel movement 1-2 x per day and they are loose.  I do know that when people have partial bowel obstructions they sometimes don't know because loose stool can still move around the obstruction so I guess he could be constipated and the articles specifically mentioned that they didn't suspect constipation.  I just feel something is not right and my search for bladder answers led me to suspect gluten but now maybe its just this.  Hopefully we get some answers. 

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. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    2. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    3. - nanny marley replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      20

      Insomnia help

    4. - David Blake commented on Scott Adams's article in Product Labeling Regulations
      1

      FDA Moves to Improve Gluten Labeling—What It Means for People With Celiac Disease

    5. - nanny marley replied to wellthatsfun's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      nothing has changed

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

    • Total Members
      133,343
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • asaT
      plant sources of calcium, such as spinach, have calcium bound to oxalates, which is not good. best source of calcium is unfortunately dairy, do you tolerate dairy? fermented dairy like kefir is good and or a little hard cheese. i do eat dairy, i can only take so much dietary restriction and gluten is hard enough! but i guess some people do have bad reactions to it, so different for everyone.  
    • asaT
      i take b12, folate, b2, b6, glycine, Nac, zinc, vk2 mk4, magnesium, coq10, pqq, tmg, creatine, omega 3, molybdnem (sp) and just started vit d. quite a list i know.  I have high homocysteine (last checked it was 19, but is always high and i finally decided to do something about it) and very low vitamin d, 10. have been opposed to this supp in the past, but going to try it at 5k units a day. having a pth test on friday, which is suspect will be high. my homocysteine has come down to around 9 with 3 weeks of these supplements and expect it to go down further. i also started on estrogen/progesterone. I have osteoporosis too, so that is why the hormones.  anyway, i think all celiacs should have homocysteine checked and treated if needed (easy enough with b vit, tmg). homocysteine very bad thing to be high for a whole host of reasons. all the bad ones, heart attack , stroke, alzi, cancer..... one of the most annoying things about celiacs (and there are so many!) is the weight gain. i guess i stayed thin all those years being undiagnosed because i was under absorbing everything including calories. going gluten-free and the weight gain has been terrible, 30#, but i'm sure a lot more went into that (hip replacement - and years of hip pain leading to inactivity when i was previously very active, probably all related to celiacs, menopause) yada yada. i seemed to lose appetite control, like there was low glp, or leptin or whatever all those hormones are that tell you that you are full and to stop eating. my appetite is immense and i'm never full. i guess decades or more ( i think i have had celiacs since at least my teens - was hospitalized for abdominal pain and diarrhea for which spastic colon was eventually diagnosed and had many episodes of diarrhea/abdominal pain through my 20's. but that symptom seemed to go away and i related it to dairy much more so than gluten. Also my growth was stunted, i'm the only shorty in my family. anyway, decades of malabsorption and maldigestion led to constant hunger, at least thats my theory. then when i started absorbing normally, wham!! FAT!!!    
    • nanny marley
      Great advise there I agree with the aniexty part, and the aura migraine has I suffer both, I've also read some great books that have helped I'm going too look the one you mentioned up too thankyou for that, I find a camomile tea just a small one and a gentle wind down before bed has helped me too, I suffer from restless leg syndrome and nerve pain hence I don't always sleep well at the best of times , racing mind catches up I have decorated my whole house in one night in my mind before 🤣 diet changes mindset really help , although I have to say it never just disappears, I find once I came to terms with who I am I managed a lot better  , a misconception is for many to change , that means to heal but that's not always the case , understanding and finding your coping mechanisms are vital tools , it's more productive to find that because there is no failure then no pressure to become something else , it's ok to be sad it's ok to not sleep , it's ok to worry , just try to see it has a journey not a task 🤗
    • nanny marley
      I agree there I've tryed this myself to prove I can't eat gluten or lactose and it sets me back for about a month till I have to go back to being very strict to settle again 
    • trents
      You may also need to supplement with B12 as this vitamin is also involved in iron assimilation and is often deficient in long-term undiagnosed celiac disease.
×
×
  • 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.