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

Help Please


Shaunta

Recommended Posts

Shaunta Newbie

Here's a little history.

I've had stomach/digestion problems all my life. I had ulcers when I was 8. When I had my son 15 years ago I had severe stomach pain (rivaling child birth, which I had just gone through) paired with terrible rotten-egg burps and follwed by vomiting and liquid stools until I felt like I would be better off dead. This happened until I stopped drinking milk. Throughout my life I've had pale, bulky, foul smelling, sticky bowel movements at least five and up to eight or more times per day.

After my 4-year-old was born, I had a sudden onset of sudden exhaustion and my hair started falling out. When I went to the doctor, he ran some thyroid tests and said not only was I not hypothyroid, I bordered on hyperthyroid (despite weighing 300 pounds and having zero energy) and blamed everything on being fat and postpartum.

It's four years later and about a two months ago the exhaustion which never left suddenly got much worse. I also started noticing a lot of gas, my hair never stopped falling out after I had my baby, and the harder I tried to lose weight the more I gained. I'd gained about 80 pounds in the past four years.

My doctor ran a lot of tests. My cholesterol was low (125), my vitamin D was alarmingly low (15) and I was also low on iron and borderline on vitamin B (I'm not sure which one.) My thyroid again showed to be not only not hypo but close to hyper.

Two weekends ago I was so exhausted (wanting to cry when my alarm went off or my baby woke up, even if I'd had 12 hours of sleep.) My husband bought me a loaf of sourdough bread and all I ate for three days was peanut butter sandwiches. By Monday morning I was in so much pain I could barely get out of bed. My back and legs were hurting enough to cause tears. I was physically ill, pale, itchy, and generally miserable. When I got to work, I googled and read about celiac and stopped eating gluten that day (last Monday.)

Wednesday I woke up with energy. Thursday I made a five hour drive without having to pull over to either use the bathroom or close my eyes because I was so tired I couldn't drive safely. It's a week now, and the weird white/yellow coating that's been on my tongue is gone, my legs and face aren't swollen anymore, my hair has stopped falling out, and despite being on my period and having a cold I have more energy than I've had since I was a kid.

Last Wednesday my doctor ordered some blood tests at my request. I'd been gluten free for two days, and she ordered me to fast before I took the tests. (The tester lady was surpised and said that this test doesn't usually require fasting.)

Here are the results:

Gliadin IgG/IgA Ab Prof, EIA

Deamidated Gliadin Abs, IgA 4.0 U/mL Limit: 0.0 - 10.0

Deamidated Gliadin Abs, IgG 0.9 U/mL Limit: 0.0 - 10.0

Endomysial Antibody IgA

Endomysial Antibody IgA Negative Negative

Can someone help me understand what this means? Does it mean I don't have Celiac? I feel so much better on the diet, I'm not planning on going back to eating gluten. But I'm curious if I can have Celiac with test levels like this. Thank you for any help.

Shaunta


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



Celiac.com Sponsor (A8-M):



RiceGuy Collaborator

Welcome to the board, and congratulations on figuring out what has been making you sick.

While I'm not an expert on the antibody tests, I do know there are often false negatives. Same with the biopsy. However, if your test results are accurate, I'd have to guess your reaction is not autoimmune, possibly more like an allergy. This may be the difference between gluten intolerance and Celiac, but I don't know for sure. That might also explain your quick recovery. I suppose though, that it may be possibly for an immune system to produce a different antibody than the ones associated with Celiac. Again, I'm no expert on it. If you never actually developed Celiac, I'd say you're quite fortunate indeed.

Either that, or you've made one incredibly fast recovery.

Being self-diagnosed, I never delved into the specifics of the blood tests. I'm sure others will have more insight for you.

ravenwoodglass Mentor

Welcome to the board. It sounds like your dropping gluten has already made a real difference in how you feel. That is usually a real good indication that you have issues with it. If you want to have a biopsy done you need to get back onto gluten until those tests are done.

I was severely ill and saw a decrease in tummy issues within days, as you did but it took a while for other stuff to improve. I hope you continue to progress smoothly.

We often have some ups and downs at first but you have come to a good place for knowledge and support. Ask any questions you need to.

Shaunta Newbie

Thanks for your responses :)

I think my main worry is that this is all in my head. Either somehow I've become a hypochondriac or else I want to feel better so badly that my brain is taking me there regardless of whether my health is actually improving. Like a placebo effect, I guess.

I don't know. I guess I wanted the blood test to tell me exactly what was wrong with me. I do feel better though. I do.

rinne Apprentice

Trust yourself, the tests may be wrong but driving for five hours and having energy again is not psychosomatic. :)

CeliBelli Newbie
....

Here are the results:

Gliadin IgG/IgA Ab Prof, EIA

Deamidated Gliadin Abs, IgA 4.0 U/mL Limit: 0.0 - 10.0

Deamidated Gliadin Abs, IgG 0.9 U/mL Limit: 0.0 - 10.0

Endomysial Antibody IgA

Endomysial Antibody IgA Negative Negative

Can someone help me understand what this means? Does it mean I don't have Celiac? I feel so much better on the diet, I'm not planning on going back to eating gluten. But I'm curious if I can have Celiac with test levels like this. Thank you for any help.

Shaunta

Shaunta,

Welcome aboard. I was diagnosed just 15 months ago, and I sympathize with you. Researching celiac disease rapidly becomes a crash course in immunology and genetics. I highly recommend that you ask your doctor for a genetics test, either by Prometheus or Kimball Labs, which are two of the best. There are several very good, in depth essays on genetics testing for celiac disease by Dr. Scot Lewey here:

https://www.celiac.com/authors/45/Dr.-Scot-Lewey

I also recommend you ask your doctor for a referral to a good gastroenterologist with experience treating celiac patients and discuss with them doing an endoscopy to biopsy your small intestine. That is considered the gold standard for diagnosis of celiac disease. You will not want to go completely gluten-free until you have that procedure done, as you will begin to heal rapidly, as you've already learned. Given your extensive medical problems, I urge you to get all of this done as quickly as scheduling allows.

Why go to all this trouble, if just going gluten-free seems to do the trick? Because celiac disease can be serious, even life threatening, and if you do indeed have it, you want the medical proof in hand in the form of official medical diagnosis. You may need this when dealing with doctors and hospitals in the future, since they will not give much credence to someone who is self-diagnosed. The other reason is that if you are celiac, you must follow a very strict gluten-free diet, and this is not easy. It is well worth it if you are celiac; but it may be an unnecessary burden if you are not.

More importantly, if all the testing indicates you are not likely to have celiac disease, you will still want to pursue answers about what you do have, particularly if living gluten-free helps. Gluten may or may not be the culprit, but it may be a clue. Getting these answers brings burdens and responsibility, but it also brings immensely liberating relief, too.

I wish you all the luck finding answers and getting diagnosed. Hang in and persevere. You are worth it.

mushroom Proficient
I think my main worry is that this is all in my head. Either somehow I've become a hypochondriac .....

Good golly, Ms.Molly. Don't let the doubters get to you. We get enough of that nonsense from our doctors and families without starting to spout it ourselves :ph34r: Only you know how your body reacts to things; you live in it every day.


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
      131,536
    • Most Online (within 30 mins)
      7,748

    Flibertygibbet
    Newest Member
    Flibertygibbet
    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

    • 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.  
    • Celiac50
      That sounds so very likely in my case! I will absolutely ask my doctor on my next bone check coming up in March... Thanks a lot! 
    • trents
      Calcium levels as measured in the blood can be quite deceiving as the body will rob calcium from the bones to meet demands for it by other bodily functions. Also, supplementing with calcium can be counterproductive as it tends to raise gut pH and decrease absorption. More often than not, the problem is poor absorption to begin with rather than deficiency of intake amounts in the diet. Calcium needs an acidic environment to be absorbed. This is why so many people on PPIs develop osteoporosis. The PPIs raise gut pH. And some people have high gut PH for other reasons. Low pH equates to a more acidic environment whereas high pH equates to a more basic (less acidic) environment.
    • Celiac50
      Kind thanks for all this valuable information! Since my Folate was/is low and also my Calcium, there IS a chance I am low in B vitamins... My doctor only measured the first two, oh and Zinc as I has twisted her arm and guess what, that was mega low too. So who knows, until I get myself tested properly, what else I am deficient in... I did a hair mineral test recently and it said to avoid All sources of Calcium. But this is confusing for me as my Ca is so low and I have osteoporosis because of this. It is my Adjusted Ca that is on the higher side and shouldn't be. So am not sure why the mineral test showed high Ca (well, it was medium in the test but relative to my lowish Magnesium, also via hair sample, it was high I was told). But anyway, thanks again for the VitB download, I will look into this most certainly!
    • ElisaAllergiesgluten
      Hello good afternoon, I was wondering if anyone has ever brought their anti-allergy pills? I have been wanting to use their Cetirizine HCI 10mg. They are called HealthA2Z and distributed by Allegiant Health.I’m also Asthmatic and these allergies are terrible for me but I also want to be sure they don’t have any sort of gluten compound.    I have tried calling them but to no avail. Has anyone ever used them? If so, did you had any problems or no problems at all?    thank you
×
×
  • 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.