Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Celiac.com!
    eNewsletter
    Donate

Is It Worth Seeing A Doc If Not On Gluten Normally?


brendab

Recommended Posts

brendab Contributor

So I am almost convinced my 2 year old has a gluten intolerance if not Celiac and I would like the official diagnosis but I don't want him on gluten for weeks if it's a "maybe" or a negative altogether. He's only 2 and I took him off wheat at 4 months of age (he was exclusively breastfed so I was really the one off of wheat for his delayed allergies) and I suspect he had gluten issues when his siblings had something that they dropped or left on the table and he ate it but I never really put it together nor did I think gluten exposure. I did a trial of barley the other day as he's not tested positive for barley allergy, just so I could see if gluten bugged him and he had yellow, moth-ball smelling poop with a HUGE amount in the diaper and lots of undigested food. I'd say that was a definite reaction but that was the ONLY exposure I did on purpose, normally it's naturally avoided with him so the damage to his villi most likely won't be there and the blood test will probably be negative.

So what I am wonder is, if I take him to a Pediatric GI will I be wasting my time and co-pay? Will there be other testing they would do? What else should I expect?

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



Jestgar Rising Star

I'm curious why you'd need an 'official' diagnosis?

Link to comment
Share on other sites
brendab Contributor

I'm curious why you'd need an 'official' diagnosis?

I'm hoping insurance will help pay for food at least and am hoping there are other benefits as well. I feel like I am lying if I say that my son and I have Celiac's if it's not been proved and diagnosed. I'm overly honest that way, is that lame? LOL

Link to comment
Share on other sites
kareng Grand Master

Where I live, an official dx is needed to get official help in school. I think most teachers would help without it. I have heard on here that colleges require notes from doctors for gluten-free food in dorms. And even then, some of them won't honor that. I have used my official note from my doctor to take food in places that don't allow that normally. Some places we have just said "food allergy" and that is enough.

Link to comment
Share on other sites
mario Explorer

I'm hoping insurance will help pay for food at least and am hoping there are other benefits as well. I feel like I am lying if I say that my son and I have Celiac's if it's not been proved and diagnosed. I'm overly honest that way, is that lame? LOL

You did get an official diagnosis.... Yellow poop

Link to comment
Share on other sites
brendab Contributor

You did get an official diagnosis.... Yellow poop

Is yellow poop only reserved for Celiac's or do you think it may be another intestinal disorder/disease? I certainly would want it treated right, I guess I have to also remember the gluten that was given and yellow poop was the result. I am still learning :)

Link to comment
Share on other sites
Looking for answers Contributor

I don't think insurance will help cover food (hopefully someone will chime in if I'm wrong, but I've never heard of that). It's almost better not to have it on your medical record in my opinion. If you ever need private insurance, the diagnosis could be a problem. They approve insurance based on a point system. I had my sister look it up for me once (she's an insurance broker), and Celiac diagnosis set me over my point limit - meaning I am unisurable in the private realm. Thank god for group benefits! :blink:

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



brendab Contributor

I don't think insurance will help cover food (hopefully someone will chime in if I'm wrong, but I've never heard of that). It's almost better not to have it on your medical record in my opinion. If you ever need private insurance, the diagnosis could be a problem. They approve insurance based on a point system. I had my sister look it up for me once (she's an insurance broker), and Celiac diagnosis set me over my point limit - meaning I am unisurable in the private realm. Thank god for group benefits! :blink:

Yikes! Really????? I have so much to think about, I am not sure where to start!

Link to comment
Share on other sites
Gardening Apprentice

I thought that with the new healthcare bill, pre-existing conditions were no longer a problem for getting health insurance?

A diagnosis might be helpful/needed for school. She may need accomodations for issues like cross-contamination, art supples (play-doh, glue, etc), she'll need her own food everytie there's a borthday celebration or a pizza party... And then most colleges require you to purchase a full meal plan the first year - which may not work for a celiac.

Link to comment
Share on other sites
brendab Contributor

I thought that with the new healthcare bill, pre-existing conditions were no longer a problem for getting health insurance?

A diagnosis might be helpful/needed for school. She may need accomodations for issues like cross-contamination, art supples (play-doh, glue, etc), she'll need her own food everytie there's a borthday celebration or a pizza party... And then most colleges require you to purchase a full meal plan the first year - which may not work for a celiac.

For now I home school my children for many different reasons, one being many food allergies and this would be just one more for our family. I'm interested to see what else others have to say in their experiences as well. I'm just not wanting to put him through being sick to maybe get a positive result. I wish there was another way :(

Link to comment
Share on other sites
my3monkees Rookie

For now I home school my children for many different reasons, one being many food allergies and this would be just one more for our family. I'm interested to see what else others have to say in their experiences as well. I'm just not wanting to put him through being sick to maybe get a positive result. I wish there was another way :(

I wanted to let you know you are not alone!

I am in the same boat. My 13 has a "tentative" Celiac diagnosis since the ped and I decided not to put her through the scope and her blood work was negative. So it is in her medical record the doctor would back me up and still I find myself saying tentative instead of just saying, yes she has Celiac. Just because she doesn't have that gold standard diagnosis. Which is ridiculous, as she is as text book Celiac as you can get! She told us she would starve rather than go back to eating gluten for the challenge. Two years later, she still says the same thing. She was so tired of being sick and miserable, I can't blame her. So we will go without that official diagnoses, unless she wants it when she is older.

Now I am starting down the same road with my 7 yr. old.

I feel for you, we also homeshool, so we don't have to worry about dealing with the school either.

Hope you get it worked out!

Link to comment
Share on other sites
brendab Contributor

I wanted to let you know you are not alone!

I am in the same boat. My 13 has a "tentative" Celiac diagnosis since the ped and I decided not to put her through the scope and her blood work was negative. So it is in her medical record the doctor would back me up and still I find myself saying tentative instead of just saying, yes she has Celiac. Just because she doesn't have that gold standard diagnosis. Which is ridiculous, as she is as text book Celiac as you can get! She told us she would starve rather than go back to eating gluten for the challenge. Two years later, she still says the same thing. She was so tired of being sick and miserable, I can't blame her. So we will go without that official diagnoses, unless she wants it when she is older.

Now I am starting down the same road with my 7 yr. old.

I feel for you, we also homeshool, so we don't have to worry about dealing with the school either.

Hope you get it worked out!

Thank you for your input, we may or may not simply say he is Celiac just to simplify things. I was thinking today that if we told people he's intolerant they may not take much notice but when people hear the word disease, they tend to take notice and greater care.

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,210
    • Most Online (within 30 mins)
      7,748

    Sue Barnett
    Newest Member
    Sue Barnett
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      You have three celiac disease specific antibody tests that are positive: Endomysial  Antibody IGA (aka, EMA), tTG-IGA, and tTG_IGG. Furthermore, your Immunoglobulin A at 55 is low, meaning you are IGA deficient. This one is not an antibody test for celaic disease per se but a measure of "total IGA" levels and if low (yours is low) it can suppress the individual antibody scores and even cause false negatives. So, yes, it definitely looks like you have celiac disease.   Do not yet begin a gluten free diet as your physician may refer you to a GI doc for an endoscopy/biopsy of the small bowel lining for confirmation of the antibody testing. This may help:   
    • Bayb
      Hi, I received my labs via email yesterday and have not heard back from my doctor yet. Can anyone tell me if these results indicate I have Celiac?      Endomysial Antibody IgAPositive  Ft-Transglutaminase (tTG) IgA6  H0-3 (U/mL) - Negative 0 - 3 - Weak Positive 4 - 10 - Positive >10 - Tissue Transglutaminase (tTG) has been identified as the endomysial antigen. Studies have demonstrated that endomysial IgA antibodies have over 99% specificity for gluten-sensitive enteropathy. FImmunoglobulin A, Qn, Serum55  L87-352 (mg/dL) Ft-Transglutaminase (tTG) IgG183  H0-5 (U/mL) - Negative 0 - 5 - Weak Positive 6 - 9 - Positive >9
    • Aussienae
      Mine is definitely triggered by inflammation and stress! I do also have arthritis in my spine, but the pain is more in my pelvic area. Im sure i have other food intolerances or other autoimmune isues but the more I focus on it and see doctor after doctor, it just gets worse.  Best thing is get of Gluten! (I also avoid lactose). Try to limit stress and anything that causes inflammation in your body.
    • ButWhatCanIEat
      Good morning,   I got an email about replies to this post. Some of my doctors had blamed a slipped disc for the pain I had and that contributes, but after meeting with a gastroenterologist AGAIN and trying some lifestyle modifications, I found out I have IBS and can't tolerate corn or excessive fructose to any degree. Cutting out corn AFTER having cut out all gluten containing products was a real pain but I feel much better now!
    • trents
      So, I contacted Scott Adams, the author of that article and also the creator/admin of this website, and pointed out to him the need to clarify the information in the paragraph in question. He has now updated the paragraph and it is clear that the DGP-IGA does serve the purpose of circumventing the false negatives that IGA deficiencies can generate in the tTG-IGA antibody test.
×
×
  • Create New...