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 Our Content
    eNewsletter
    Donate

Just Got Back Celiac Panel Results Back


Cheli

Recommended Posts

Cheli Newbie

I sent my 6 year old to the doc because he was having tummy problems. I asked him to do a Celiac Panel and it came back at 193. the range is 33-200. So my question is this borderline? Should I just drop the issue? What should I do? The doc now thinks he might have consipation because we had an x-ray done that showed that he was backed up. That is what the doc thinks is the problem is. I don't buy it.

Thanks, Cheli


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

Did he only give you one number? There should have been several.

Did he tell you what that number was testing?

It doesn't hurt anyone to go gluten-free, but it's a lot of work if you don't need it! If he's backed up, you can see what happens once the constipation issue is resolved.

chrissy Collaborator

i didn't know any of the tests had a range like that----i guess it must depend on the way the lab does their testing?? i agree with carla---work on the constipation issue---the x-ray shows that it is definitely an issue---but not what is causing it. also, ask for copies of his test reslults.

Cheli Newbie

All the test reads is

Discription Value Ref. Range Units

IMMUNOGLOBULIN A 193 33-200 mg/dL

Oh I just read that fine print :-)

Tissue Transglutaminase Antibody, IgA to follow.

What does that mean? How long will this take? What should I look out for when we do get it?

Sorry, don't know much about the tests. I do know about Celiac because my bestfriend's mom has it. She is in the last stage of it.

Thanks again,

Cheli

Rachel--24 Collaborator
All the test reads is

Discription Value Ref. Range Units

IMMUNOGLOBULIN A 193 33-200 mg/dL

Oh I just read that fine print :-)

Tissue Transglutaminase Antibody, IgA to follow.

What does that mean? How long will this take? What should I look out for when we do get it?

This isnt enough to rule out Celiac. The TtG is more specific....I have no idea why it says TtG to follow?? Usually all the results come back together. The Celiac panel consists of 5 different tests. You only have the results for one test.

Cheli Newbie

I guess I will have to just wait and see if the doc calls me and lets me know when he gets the others.

Cheli

Ursa Major Collaborator

Cheli, I agree with the others. Your doctor should have done five tests, not just two, and it's weird that you don't have at least those two back together. And constipation can be caused by celiac disease, not just diarrhea. So, your son's bowels being backed up could be a symptom of celiac disease. But it should be looked after for sure.

What do you mean by your best friend's mom is in the last stage of celiac disease? There is no last stage, unless you're not eating gluten-free! If you consume no gluten, you will be healthy with celiac disease (unless you were diagnosed very late in life, and developed a bunch of autoimmune diseases on top of celiac disease).


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



Celiac.com Sponsor (A8-M):



Cheli Newbie

She was told late in life. She does eat gluten free food but has gotten bad stuff before. She can not have any of her food touch anything that has been touched by things with Gluten in it. She can get an attack but just by touching a counter top that might have had non gluten free food on it. She has to use gluten free stuff on her skin because she can get sick. She really has it bad. She can loose so much weight when this happens. She has lost up to 40lbs in one attack. The doc told her that she has it very bad.

Cheli

CarlaB Enthusiast

There are many of us who are pretty sensitive. Anyone eating gluten-free has to keep their food away from crumbs. Think of the flu -- it doesn't matter how much of the bug you are exposed to, you get sick -- it's similar with celiac. After you get off gluten, you get pretty ill when you eat it, even a small amount.

Some people are bothered by products for the skin, some are not. All of us avoid things that can get in our mouths like shampoo, lipstick, etc. I get a rash on my scalp if I use shampoo with wheat in it. But, it wouldn't bother me to touch something like bread, etc., only something that stays on my skin for a time. I prefer not to touch bread and do not prepare food with gluten for my family because of the danger of getting it into my food.

It sounds like hers was very progressed, meaning she probably had a lot of damage. I was fortunate to catch mine before a lot of damage was done.

Ursa Major Collaborator
She was told late in life. She does eat gluten free food but has gotten bad stuff before. She can not have any of her food touch anything that has been touched by things with Gluten in it. She can get an attack but just by touching a counter top that might have had non gluten free food on it. She has to use gluten free stuff on her skin because she can get sick. She really has it bad. She can loose so much weight when this happens. She has lost up to 40lbs in one attack. The doc told her that she has it very bad.

Cheli

Actually Cheli, that is the way all of us are! You either have it, or you don't. She doesn't have it bad, this is NORMAL for all of us! We ALL have to use gluten free shampoo, conditioner, soap, lotion, toothpaste, lipstick etc.

None of us can have any food that has been touched by something containing gluten, it would make us sick. If your son really has celiac disease, this is the way it will be for him, too. You will have to buy a new toaster for his gluten free bread, you will NEVER be able to just take a hamburger patty out of a bun for him to eat, or take croutons off a salad, as the patty or the salad would make him sick. You would have to buy a new cutting board, just to make his food, new cooking spoons (if you have wooden ones), you'll need to replace (or have his own) scratched non-stick cookware, as well as your plastic strainer, as you cannot clean it completely of the gluten from regular noodles.

You would need to read every label of any food you buy to avoid hidden gluten. You would not be able to use peanut butter, mayonaise, butter or jam for him, if somebody has put a knife back into one of those, after spreading those things on regular bread. You can't use the same knife to make his sandwich after making yours. You can't stir his food with the same cooking spoon you just used to stir something containing gluten.

That is NORMAL life, every day, for EVERYBODY with celiac disease. I guess, in this lady's doctors mind, we all 'have it bad' then.

Her doctor sounds very ignorant. Unfortunately, many doctors are very ignorant of celiac disease.

Daxin Explorer

I can only speak for me, but my blood work had 4 antibodies on it.

One of the results was triple the normal range, and one other was almost double. The other 2 were what the doctor said were considered "equivical", meaning that based on the symptoms I had given him and his own observations (everything BUT a biopsy) could be taken to be celiac. There were other blood tests leading up to this last one a few weeks ago.

AS far as how long does it take? I was told it should only take about 4 days.

Ursa Major Collaborator
AS far as how long does it take? I was told it should only take about 4 days.

Wow, only four days? Here in Canada it takes four to six weeks! It seems when it comes to anything medical, they won't do anything fast and in a timely manner.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,198
    • Most Online (within 30 mins)
      7,748

    Jamie0230
    Newest Member
    Jamie0230
    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

    • Scott Adams
      Clearly from what you've said the info on Dailymed is much more up to date than the other site, which hasn't been updated since 2017. The fact that some companies might be repackaging drugs does not mean the info on the ingredients is not correct.
    • RMJ
      To evaluate the TTG antibody result we’d need to know the normal range for that lab.  Labs don’t all use the same units.  However, based on any normal ranges that I’ve seen and the listed result being greater than a number rather than a specific number, I’d say yes, that is high! Higher than the range where the test can give a quantitative result. You got good advice not to change your diet yet.  If you went gluten free your intestines would start to heal, confusing any further testing,
    • Bev in Milw
      Scott is correct….Thank you for catching that!      Direct link for info  of fillers.    http://www.glutenfreedrugs.com/Excipients.htm Link is on 2nd page  of www.glutenfreedrugs.com   Site was started by a pharmacist (or 2) maybe 15-20 yrs ago with LAST updated in  2017.  This makes it’s Drug List so old that it’s no longer relevant. Companies & contacts, along with suppliers &  sources would need to be referenced, same amount effort  as starting with current data on DailyMed      That being said, Excipient List is still be relevant since major changes to product labeling occurred prior ’17.           List is the dictionary that sources the ‘foreign-to-us’ terms used on pharmaceutical labels, terms we need to rule out gluten.    Note on DailyMed INFO— When you look for a specific drug on DailyMed, notice that nearly all of companies (brands/labels) are flagged as a ‘Repackager’… This would seem to suggest the actual ‘pills’ are being mass produced by a limited number of wholesaler suppliers (esp for older meds out of  patent protection.).      If so, multiple repackager-get  bulk shipments  from same supplier will all  be selling identical meds —same formula/fillers. Others repackager-could be switching suppliers  frequently based on cost, or runs both gluten-free & non- items on same lines.  No way to know  without contacting company.     While some I know have  searched pharmacies chasing a specific brand, long-term  solution is to find (or teach) pharmacy staff who’s willing help.    When I got 1st Rx ~8 years ago, I went to Walgreens & said I needed gluten-free.  Walked  out when pharmacist said  ‘How am I supposed  to know…’  (ar least he as honest… ). Walmart pharmacists down the block were ‘No problem!’—Once, they wouldn’t release my Rx, still waiting on gluten-free status from a new supplier. Re: Timeliness of DailyMed info?   A serendipitous conversation with cousin in Mi was unexpectedly reassuring.  She works in office of Perrigo, major products of OTC meds (was 1st to add gluten-free labels).  I TOTALLY lucked out when I asked about her job: “TODAY I trained a new full-time employee to make entries to Daily Med.’  Task had grown to hours a day, time she needed for tasks that couldn’t be delegated….We can only hope majorities of companies are as  conscientious!   For the Newbies…. SOLE  purpose of  fillers (possible gluten) in meds is to  hold the active ingredients together in a doseable form.  Drugs  given by injection or as IV are always gluten-free!  (Sometimes drs can do antibiotics w/ one-time injection rather than 7-10 days of  pills .) Liquid meds (typically for kids)—still read labels, but  could be an a simpler option for some products…
    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
×
×
  • Create New...