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

Possibility Of Celiac Disease?


zs1994

Recommended Posts

zs1994 Newbie

Hi all,

I'm new to this forum. I have a diabetic sister who was also diagnosed with celiac a year ago. For the past week or so I've had an upset stomach without fever. Symptoms are:

- lack of appetite and weight loss

- stomach gas, burping & flatulence

- loose stools, sometimes diaherrea

- bloating after eating and stomach noises

Went to the doctor and he said it's most likely a stomach virus or bug but he's ordered a blood test for celiac screening because my sister has it.

I wanted to ask what the likelihood is of me having celiac? I know only the testing will confirm but do my symptoms hint of it and can symptoms come on all of a sudden? I'm 21 and usually healthy. Thanks all!


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

Welcome! Read this link from the University of Chicago. It is good to be tested every few years (even without symptoms) or as symptoms develop.

Open Original Shared Link

zs1994 Newbie

Welcome! Read this link from the University of Chicago. It is good to be tested every few years (even without symptoms) or as symptoms develop.

Open Original Shared Link

Hi thank you for the quick reply, i understand it makes sense for me to be tested. Is the blood test usually accurate?

cyclinglady Grand Master

Well, it is not perfect, but what is? You should get copies of your sister's results and at least make sure you are getting the same tests. For example, my doctor ran the entire panel and I only tested positive on one (DGP IGA) and negative on the rest yet biopsies revealed a Marsh Stage IIIB (mod to severe intestinal damage). So, my kid gets the complete panel and not just the TTg and IGA deficiency celiac screening tests (cheapest/basic and in all fairness catches 95% of celiacs) because of my tests. I am getting the rest of my family tested again since they all got the basic screening.

You might test negative like my kid, but you will need to get tested every few years. That is the standard procedure when you have a first-degree relative with celiac disease.

Good to keep on top of your health! My goal is to prevent my kid and younger relatives from doing severe damage to their bodies and suffering needlessly!

Always keep records of your lab tests in case you change doctors or need to share with other family members in order to get them tested.

zs1994 Newbie

Wow, thats an extremely informative post, thank you very much. I'll make a note of comparing my results and test paremeters with my sister's data. As for now, I guess it's nothing other than a really anxious wait!

cyclinglady Grand Master

Here are the tests for celiac disease:

-Tissue Transglutaminase (tTG) IgA and (tTG) IgG

-Deamidated Gliadin Peptide (DGP) IgA and (DGP) IgG

-EMA IgA

-total serum IgA and IgG (control test)

-AGA IGA and AGA IgG - older and less reliable tests largely replace by the DGP tests

-endoscopic biopsy - make sure at least 6 samples are taken

(Source: NVSMOM -- )

zs1994 Newbie

Here are the tests for celiac disease:

-Tissue Transglutaminase (tTG) IgA and (tTG) IgG

-Deamidated Gliadin Peptide (DGP) IgA and (DGP) IgG

-EMA IgA

-total serum IgA and IgG (control test)

-AGA IGA and AGA IgG - older and less reliable tests largely replace by the DGP tests

-endoscopic biopsy - make sure at least 6 samples are taken

(Source: NVSMOM -- )

Many thanks again, i'm from the UK by the way, i don't think they perform that many tests. From what I've read the main test performed here is Tissue Transglutaminase (tTG) IgA and (tTG) IgG.


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



Celiac.com Sponsor (A8-M):



zs1994 Newbie

It's been almost 2 weeks since my symptoms began. I'm convinced i'm a Celiac! Don't really have any abdominal pain and my gas and bloating has reduced but my loose stools haven't stopped. Most of the time they are loose and a few times actual diaherrea. But the main thing is they always float. Sorry about the detailed info! Can anyone relate to this?

ravenwoodglass Mentor

Since this is still going on an appointment with your doctor would be a good idea. You need to be screened for celiac anyway with a sister that has it and it would also be a good idea for your doctor to test your stool for food poisoning or a bacterial infection.

gilligan Enthusiast

Before I was diagnosed, I had the very same symptoms at you.  They just cropped up out of the blue and wouldn't go away.  I was sure I was just run down and tired after a trying summer and start to the school year. After about 4 months (and Christmas break - I teach), I went to my gp who sent me to a g.i.  Yep, celiac!

squirmingitch Veteran

And don't stop eating a full gluten diet until ALL testing is completed otherwise it invalidates the tests.

binkman Rookie

Hi zs1994,

I had the same symptoms as you before my diagnosis. I'd been having them more and more frequently in the weeks leading up to my diagnosis but looking back now I can see that I'd been developing them on and off for a few months. They got really bad, and I started to get headaches and nerve pain in my feet, but I started to recover almost immediately after going gluten free. It takes some people a bit longer, but you have every reason to be optimistic. Good luck!

csa2015 Newbie

My wife has Celiac and the blood test was negative but after giving her history to a infectious disease specialist, she was diagnosed with Celiac. She went on a gluten-free diet despite the test and was back to normal in a week. Then she was accidentally contaminated and discovered the cause after getting sick again. Then later she did a gluten challenge test and was very sick about 5 hours after eating the gluten. Usually the tests are pretty accurate but not always.

Victor10 Rookie

Same thing happened to me, like exact. I'm also sure I have celiac. Thinking about it and my past with stomach issues makes sense now. Going to the doctor this Tues to get some tests done.

zs1994 Newbie

Thanks for all the replies, much appreciated. As easy as it is to worry that you may have Celiac, there are a few conditions out there that mimic Celiac symptoms, namely Giardia or related parasite/viral infections which can last a few weeks or even IBS. If my sister was not a Celiac, I wouldn't have got myself tested.

  • 2 weeks later...
zs1994 Newbie

Hi all

My doctor called me and said my blood test came back perfectly normal. My symptoms have all but gone and my stools have returned to normal too. Still have a little gas now and then but the one problem that remains is that I've lost my appetite or hunger I should say. Does this warrant a trip back to the doctor? I aim to get my blood test results printed out too. 

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. - Mmoc replied to Mmoc's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Blood tests low iGA 4 years later digestive issues

    2. - Aretaeus Cappadocia replied to Clear2me's topic in Gluten-Free Foods, Products, Shopping & Medications
      6

      Gluten free nuts

    3. - trents replied to Larzipan's topic in Related Issues & Disorders
      42

      Has anyone had terrible TMJ/ Jaw Pain from undiagnosed Celiac?

    4. - Scott Adams replied to Larzipan's topic in Related Issues & Disorders
      42

      Has anyone had terrible TMJ/ Jaw Pain from undiagnosed Celiac?

    5. - Wheatwacked commented on Scott Adams's article in Latest Research
      6

      Study Estimates the Costs of Delayed Celiac Disease Diagnosis (+Video)


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,387
    • Most Online (within 30 mins)
      7,748

    LizzieE
    Newest Member
    LizzieE
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Mmoc
      Thank you kindly for your response. I have since gotten the other type of bloods done and am awaiting results. 
    • Aretaeus Cappadocia
      I wanted to respond to your post as much for other people who read this later on (I'm not trying to contradict your experience or decisions) > Kirkland Signature Super Extra-Large Peanuts, 2.5 lbs, are labeled "gluten free" in the Calif Costcos I've been in. If they are selling non-gluten-free in your store, I suggest talking to customer service to see if they can get you the gluten-free version (they are tasty) > This past week I bought "Sliced Raw Almonds, Baking Nuts, 5 lbs Item 1495072 Best if used by Jun-10-26 W-261-6-L1A 12:47" at Costco. The package has the standard warning that it was made on machinery that <may> have processed wheat. Based on that alone, I would not eat these. However, I contacted customer service and asked them "are Costco's Sliced Almonds gluten free?" Within a day I got this response:  "This is [xyz] with the Costco Member Service Resolutions Team. I am happy to let you know we got a reply back from our Kirkland Signature team. Here is their response:  This item does not have a risk of cross contamination with gluten, barley or rye." Based on this, I will eat them. Based on experience, I believe they will be fine. Sometimes, for other products, the answer has been "they really do have cross-contamination risk" (eg, Kirkland Signature Dry Roasted Macadamia Nuts, Salted, 1.5 lbs Item 1195303). When they give me that answer I return them for cash. You might reasonably ask, "Why would Costco use that label if they actually are safe?" I can't speak for Costco but I've worked in Corporate America and I've seen this kind of thing first hand and up close. (1) This kind of regulatory label represents risk/cost to the company. What if they are mistaken? In one direction, the cost is loss of maybe 1% of sales (if celiacs don't buy when they would have). In the other direction, the risk is reputational damage and open-ended litigation (bad reviews and celiacs suing them). Expect them to play it safe. (2) There is a team tasked with getting each product out to market quickly and cheaply, and there is also a committee tasked with reviewing the packaging before it is released. If the team chooses the simplest, safest, pre-approved label, this becomes a quick check box. On the other hand, if they choose something else, it has to be carefully scrutinized through a long process. It's more efficient for the team to say there <could> be risk. (3) There is probably some plug and play in production. Some lots of the very same product could be made in a safe facility while others are made in an unsafe facility. Uniform packaging (saying there is risk) for all packages regardless of gluten risk is easier, cheaper, and safer (for Costco). Everything I wrote here is about my Costco experience, but the principles will be true at other vendors, particularly if they have extensive quality control infrastructure. The first hurdle of gluten-free diet is to remove/replace all the labeled gluten ingredients. The second, more difficult hurdle is to remove/replace all the hidden gluten. Each of us have to assess gray zones and make judgement calls knowing there is a penalty for being wrong. One penalty would be getting glutened but the other penalty could be eating an unnecessarily boring or malnourishing diet.
    • trents
      Thanks for the thoughtful reply and links, Wheatwacked. Definitely some food for thought. However, I would point out that your linked articles refer to gliadin in human breast milk, not cow's milk. And although it might seem reasonable to conclude it would work the same way in cows, that is not necessarily the case. Studies seem to indicate otherwise. Studies also indicate the amount of gliadin in human breast milk is miniscule and unlikely to cause reactions:  https://www.glutenfreewatchdog.org/news/gluten-peptides-in-human-breast-milk-implications-for-cows-milk/ I would also point out that Dr. Peter Osborne's doctorate is in chiropractic medicine, though he also has studied and, I believe, holds some sort of certifications in nutritional science. To put it plainly, he is considered by many qualified medical and nutritional professionals to be on the fringe of quackery. But he has a dedicated and rabid following, nonetheless.
    • Scott Adams
      I'd be very cautious about accepting these claims without robust evidence. The hypothesis requires a chain of biologically unlikely events: Gluten/gliadin survives the cow's rumen and entire digestive system intact. It is then absorbed whole into the cow's bloodstream. It bypasses the cow's immune system and liver. It is then secreted, still intact and immunogenic, into the milk. The cow's digestive system is designed to break down proteins, not transfer them whole into milk. This is not a recognized pathway in veterinary science. The provided backup shifts from cow's milk to human breastmilk, which is a classic bait-and-switch. While the transfer of food proteins in human breastmilk is a valid area of study, it doesn't validate the initial claim about commercial dairy. The use of a Dr. Osborne video is a major red flag. His entire platform is based on the idea that all grains are toxic, a view that far exceeds the established science on Celiac Disease and non-celiac gluten sensitivity. Extraordinary claims require extraordinary evidence, and a YouTube video from a known ideological source is not that evidence."  
    • Wheatwacked
      Some backup to my statement about gluten and milk. Some background.  When my son was born in 1976 he was colicky from the beginning.  When he transitioned to formula it got really bad.  That's when we found the only pediactric gastroenterologist (in a population of 6 million that dealt with Celiac Disease (and he only had 14 patients with celiac disease), who dianosed by biopsy and started him on Nutramegen.  Recovery was quick. The portion of gluten that passes through to breastmilk is called gliadin. It is the component of gluten that causes celiac disease or gluten intolerance. What are the Effects of Gluten in Breastmilk? Gliaden, a component of gluten which is typically responsible for the intestinal reaction of gluten, DOES pass through breast milk.  This is because gliaden (as one of many food proteins) passes through the lining of your small intestine into your blood. Can gluten transmit through breast milk?  
×
×
  • 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.