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

So Confused....


shan1523

Recommended Posts

shan1523 Rookie

Ok, mini-history...ds Noah started solids at 5 months age, reacted badly to oatmeal and barley cereal, rash, distended belly, screaming in pain and diarrhea, so we took him off gluten...well except I didnt know all hidden gluten stuff, so he would have diarrhea and the rash stayed for a few more months, he was always a big boy (9.8 born at 36 weeks, yes the dates were right) so when he didnt gain any weight for a few months, the dr's didnt worry, but when he didnt grow height wise (also tall--always 98% for height) they worried ...anyways we took him totally off gluten at 9 months, after I found this site, and talked to some others about what all gluten is...he had a bite of some glutened food at 14 months and screamed in pain, got the distended belly and diarhhea....the doc did some blood work (only 2 of the 5 tests though, I have since learned) and they told me in was inconclusive (didnt say yes, but didnt say no, and wanted me to continue the diet for now since he;s young)....flash to now..he is 2 years and 4 months...Im going crazy not knowing if its celiac or gluten intolerance....(I got tested all five tests, and Im negative) his baby sister is 3 months and we are going through multiple GERD tests and milk soy protien allergy issues, she has apnea issues blah blah blah...so I figured shes going through all the tests, might as well try Noah again with gluten, and do his tests(another reason - have paid our out pocket maxs for the year so all tests would be free to us right now)

ANYWAYS, point is, he has had gluten, small amouts, but gluten none the less, for 3 days now, and no diahrea no screaming no distended belly....Im so confused, I thought he would react somehow...but does this mean he outgrew his intolerance and never had celiac?

He couldnt drink milk for 2 years, but we trialed it in June and hes doing fine...(he has milk protein intolerance issues as a baby, but thankfully outgrew them)

Im so confused..and sick of being at the doctors..my three month old was at the ER sunday, her dr Mon, we have another appt tomorrow and a test on mon......

anyone else have a toddler that suddenly has no symptoms?

Thanks

Shannon


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



Celiac.com Sponsor (A8-M):



Jestgar Rising Star

There was a study where they fed potentially Celiac babies gluten starting at different months (3-6 months, 6-9 months) and found that babies who started eating gluten sooner had more of the painful symptoms. Babies who started eating gluten later still developed the damaged villi, but didn't have the gastro symptoms.

So Noah could still have Celiac, but be in the silent phase of it.

You could try the antibody tests, or the biopsy, or just not feed him gluten, but I think feeding him gluten without finding out for sure might be doing him damage in the long run.

mommida Enthusiast

The kids don't seem to react to the accidental gluten exposures as I do. My daughter didn't seem to react for at least three or four last times, until she was just vomiting two days ago. (could have been a stomache bug, but she didn't have a fever only vomited once and has wanted to just sleep since and the brown circles under her eyes - Dr.'s call them allergy shiners)

You've got to remember that some people are asymptomatic.

You just don't know what kind of reaction you're going to get.

It is really hard trying to figure out what little ones are experiencing. My son gets brain fog so bad it scares him because he can't remember the words he wants to use, and then he can be so iiritable you just want to run away from him.

L.

shan1523 Rookie
The kids don't seem to react to the accidental gluten exposures as I do. My daughter didn't seem to react for at least three or four last times, until she was just vomiting two days ago.

Thats kinda why Im confused --in the past he has reacted to accidental glutening, and now no reaction at all...he is tired, but he also gave up naps and has a colicky/GERDling sister who keeps him awake....

I know part of me doesnt want to trial it in case Im hurting him, but then I also just want to know...like give it 2 weeks and then do the full celiac panel....

Thanks for the quick responses...

Shannon

ds Noah 6.28.04---gluten issues...now confused

dd Audrey 7.13.06---preemie, GERD, MSPI, apnea

GFBetsy Rookie

I believe that for the tests to be accurate, he'll have to be eating gluten for at least 3 months. (That's the recommendation, anyway.) If you are going to be worrying about this for years if you don't have a definitive diagnosis, then I'd suggest that you go through with the gluten challenge. My daughter's bloodwork came back "Indeterminate", but I knew it runs in the family, and I could see the symptoms she was displaying, so I took her off gluten anyway. 3 days later her diarhea was gone and she was smiling. For me, that's enough. When she does manage to eat gluten (sneaking her sister's sandwich crusts, etc.) she doesn't have any major reactions but her initial reactions make me stick with the diet. I decided that she can decide to do a gluten challenge when she gets to be 12 or so (if she wants), but until then I am going to do the best for her that I can - and that means keeping her off gluten.

That may seem like conflicting advice, but what I mean is: If you need a definitive diagnosis in order to be consistent with a gluten free diet, then do what you need to do in order to get one. Doing a gluten challenge for a few months is unlikely to kill him (although, if he does have celiac, it might lead to further food allergies because of the Leaky Gut problems celiac causes). Either way, think long and hard about it and weigh the options and then do what you need to do.

Good luck!

AndreaB Contributor

Even with going back on gluten for 3 months, it may not be long enough. Many teens and adults have suffered other intolerances and autoimmune diseases with challenges and/or not adhereing to the diet.

If you can, try enterolab. You can do the whole gluten panel or maybe just the gene test. If you know the genes you'll know more of what you're looking at.

Open Original Shared Link

Personally, I'm inclined to think that if he had a problem before it will manifest itself again at a later time.

shan1523 Rookie

Thanks for the replies...its just so hard, cuz I want to know, but I dont want him to suffer, my DH and I decided to stop trialing the gluten since tests are often inconclusive so young anyways (and I dont want to do the biopsy (my 3month old has to have one for gerd issues and that will be hard enough)

anyway we started to see his behavior and mood change,and he got an odd rash, not the typical DH rash, but a rash...so it was enough to know his body was reacting somehow...so we are off it again, and I dont plan on re-trying it for many many years...

I think i just had a momentary lapse of judgement on my part, I never really planned on re-intro-ing it so young, but I think Im just overwhelmed with my daughters issues I just wanted Noah's to be done...oh well...

thanks for all the replies though

Shannon


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



Celiac.com Sponsor (A8-M):



Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,543
    • Most Online (within 30 mins)
      7,748

    yfuvhg
    Newest Member
    yfuvhg
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.