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

Do You Think I Have Celiac?


Chelsea-Lynne

Recommended Posts

Chelsea-Lynne Rookie

I have had stomach issues (cramps and diarrhea) since I was young, and I used to see a gastroenterologist. I believe she did the blood tests (whatever they had in early 2000s...I don't know if it is different now) for Celiac and they came back negative. She just diagnosed me with IBS. Years later, I decided to try eating gluten free to see if it helped. I have been eating gluten free for probably about 5 to 6 years now, and I no longer have the stomach issues that I used to have. I actually deal with constipation now, but I think that could be from eating a lot of rice products. It is such a pain to eat gluten free, and people always think I don't actually have Celiac since I was never officially diagnosed with it. I can't get tested though because I have been eating gluten free for so long. Recently, my twin sister got the blood tests done for Celiac and one of them came back positive (the rest were negative). She had the same stomach issues as I did, and decided to just start eating gluten free as well. Since eating gluten free, she has noticed her toenails are clearing up (she has had a problem with them for years that look like fungus, but it always came back negative for fungus).

 

I decided to just try something with gluten tonight to see what happened. I chose something that I have been missing...Twizzlers haha. I ate one Twizzler about 1-2 hours ago, but I haven't had any stomach issues yet...is it too soon to tell? This is so weird.

 

Update: I just started to get a slight headache. Could that be from the gluten? I actually used to get a lot of headaches when I was younger before eating gluten free.


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

One Twizler might not be enough gluten to make you feel bad after 5 years gluten-free. 

IrishHeart Veteran

...yes, not enough to induce a reaction, probably.

 

And rice should not cause constipation. If you are eating lots of brown rice, you should be pretty "fibered up" and the pipes should

be running smoothly.

 

Something else is causing the big C in you. (IMHO of course.)

Chelsea-Lynne Rookie

...yes, not enough to induce a reaction, probably.

 

And rice should not cause constipation. If you are eating lots of brown rice, you should be pretty "fibered up" and the pipes should

be running smoothly.

 

Something else is causing the big C in you. (IMHO of course.)

Really? I thought a small amount would be more likely cause a reaction after so long of eating gluten free since my system isn't used to it. Yeah..I guess it could also be that I don't drink enough water.

nvsmom Community Regular

I get migraines from gluten, so I would say that it is possible the twizzler caused it...but that is a very small amount.

If your symptoms have gone while on the gluten-free diet, I think sticking with it would be wise - especially if your twin has celiac disease which makes it more likely that you do too.

As an aside, hypothyroidism (Hashimoto's) can cause C, and celiacs have a higher incidence of it than the rest of the population. If you have symptoms beyond C, you could get it checked.

Best wishes.

Chelsea-Lynne Rookie

I get migraines from gluten, so I would say that it is possible the twizzler caused it...but that is a very small amount.

If your symptoms have gone while on the gluten-free diet, I think sticking with it would be wise - especially if your twin has celiac disease which makes it more likely that you do too.

As an aside, hypothyroidism (Hashimoto's) can cause C, and celiacs have a higher incidence of it than the rest of the population. If you have symptoms beyond C, you could get it checked.

Best wishes.

 

Thanks. I actually do have hypothyroidism. I'm being treated, so my levels are fine now. 

I'm not sure if she definitely has Celiac since only one of the blood tests came back positive.

cavernio Enthusiast

Well, you definitely have the genes necessary for it, and you had celiac symptoms before you were gluten free (although we all know celiac symptoms could be any number of things), and being gluten free makes you feel better.

If you had a really noticeable reaction from eating gluten, then that's either you reacting to gluten or a placebo. (If you were really worried about a placebo wait until all symptoms go away and get a friend or family member to feed you gluten in something at some unknown point in the future.) However, having no observable reaction to eating gluten doesn't mean you don't have celiac disease. It's sort of a one way street in those regards. We see posts here of celiacs who usually react to tiny amounts of gluten but, for whatever reason, ate a piece of regular bread, and they noticed nothing. Also, people used to think that celiac disease would cure itself after a time, and then people could go back to eating gluten, because they didn't get symptoms when they ate it.

 

You once thought you were a celiac, now you even have more reason to believe you are a celiac from your twin's diagnosis...even if you're dizygotes it's still a family member with it. Her diagnosis shouldn't make you question your own self-diagnosis now, it only strengthens it.

 

Even if you decided you wanted a straight out answer, ate gluten everyday for 3 months, then got a biopsy done, you could still be gluten intolerant without being a "gold-standard" celiac and have the biopsy come back normal.

 

Yes, headaches are a fairly common symptom for celiacs. But they're also pretty common to everyone.


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



Celiac.com Sponsor (A8-M):



Chelsea-Lynne Rookie

Well, you definitely have the genes necessary for it, and you had celiac symptoms before you were gluten free (although we all know celiac symptoms could be any number of things), and being gluten free makes you feel better.

If you had a really noticeable reaction from eating gluten, then that's either you reacting to gluten or a placebo. (If you were really worried about a placebo wait until all symptoms go away and get a friend or family member to feed you gluten in something at some unknown point in the future.) However, having no observable reaction to eating gluten doesn't mean you don't have celiac disease. It's sort of a one way street in those regards. We see posts here of celiacs who usually react to tiny amounts of gluten but, for whatever reason, ate a piece of regular bread, and they noticed nothing. Also, people used to think that celiac disease would cure itself after a time, and then people could go back to eating gluten, because they didn't get symptoms when they ate it.

 

You once thought you were a celiac, now you even have more reason to believe you are a celiac from your twin's diagnosis...even if you're dizygotes it's still a family member with it. Her diagnosis shouldn't make you question your own self-diagnosis now, it only strengthens it.

 

Even if you decided you wanted a straight out answer, ate gluten everyday for 3 months, then got a biopsy done, you could still be gluten intolerant without being a "gold-standard" celiac and have the biopsy come back normal.

 

Yes, headaches are a fairly common symptom for celiacs. But they're also pretty common to everyone.

Thanks. I guess I just wish I didn't have to eat gluten free. People hate going out to eat with me since we can only go to certain places. It really stinks. :(

 

And my sister wasn't officially diagnosed with Celiac, though.

mushroom Proficient

Thanks. I guess I just wish I didn't have to eat gluten free. People hate going out to eat with me since we can only go to certain places. It really stinks. :(

 

And my sister wasn't officially diagnosed with Celiac, though.

 

We all think it would be nice if we didn't have to eat gluten free :)  but that's not the reality.  We have to deal with what is as much as possible, not what we wish it would be. 

 

It is not necessary for all celiac tests to be positive ~~ one is enough.  The tests all exist because not all of them will pick it up; some catch the disease earlier than others, there are a lot of variables involved in celiac testing.  If they were all required to be positive very few people would be diagnosed. 

 

And you do have another autoimmune disease... I think it is probably time to accept it for what it is :)   Now, if you noticed no improvement gluten free (totally) after three months, THEN you could re-evaluate.

cavernio Enthusiast

I got a biopsy because I wanted to be treated seriously as a patient by doctors. I asked the GI, who was saying I should get a biopsy, multple times about other reasons why my blood tests could have shown up positive, and he dodged the question every time.

IrishHeart Veteran

Thanks. I guess I just wish I didn't have to eat gluten free. People hate going out to eat with me since we can only go to certain places. It really stinks. :(

 

And my sister wasn't officially diagnosed with Celiac, though.

 

I use the app Find Me Gluten Free to find plenty of places to eat out. There are more options than you may think! and my WE friends (wheat eaters) and I can dine out together.  :) do not despair. 

IrishHeart Veteran

I got a biopsy because I wanted to be treated seriously as a patient by doctors. I asked the GI, who was saying I should get a biopsy, multple times about other reasons why my blood tests could have shown up positive, and he dodged the question every time.

 

 

Crohn's and other inflammatory bowel diseases can sometimes raise the TTG levels, according to my GI, which is why he does a work up for all inflammatory bowel diseases when he suspects celiac, but blood work is not conclusive or symptoms are atypical. 

  • 2 weeks later...
Chelsea-Lynne Rookie

I just got a copy of my twin sister's bloodwork, and these are her results:

 

Anti-Endomysial: normal

Gliadin IGG: 47 HI

Gliadin IGA: normal

 

Do you think she has a good chance of actually having Celiac or no?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,546
    • Most Online (within 30 mins)
      7,748

    KimberlyAnne76
    Newest Member
    KimberlyAnne76
    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
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • 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.
×
×
  • 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.