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Does This Sound Like Celiac? Please Help!


leethinker

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leethinker Rookie

Hi everyone,

I've posted here before. I recently had an endoscopy done. Unfortunately, it was not to test for celiac, but rather just to see if there was anything else going on in there like cancer. Luckily everything was good except for mild gastritis. I've done a blood test IgE which showed that I definitely have a "food allergy". That was 650 when it should be under 100. My doc said my symptoms are from the food allergy and I should just go home and test it out myself through an elimination diet.

These are my symptoms, all of which developed while I was pregnant with my second child:

- Slightly elevated bilirubin levels

- Pain in upper abdomen (almost always), including a very annoying pain under my left rib.

- CHRONIC constipation. (I am not exaggerating!)

- EXTREME tiredness all the time.

- Headaches.

- Very dry excema on my hands, inbetween my fingers.

- Joint pains (my knees are suddenly grinding even though I am thin and do no sports at all; my right shoulder hurts all the time, and started hurting around the time the rest of my symptoms developed.)

- Mouth ulcers/canker sores in my mouth, & cracked corners of my lips (this happens occassionally)

- Mild depression and relatively strong anxiety which I cannot explain logically

- Major trouble concentrating. (I often say I feel like I have ADD)

- Blurry vision even though my eyesight is nearly 20-20

- My skin every so often starts to hurt really bad, like it's burning. It hurts to even touch slightly. It's really strange. It will just start up and then last for a day, and then return to normal. Really wierd.

I'm going to a medical doctor who is also a homeopath on Monday, and I am really hoping she will test me for celiac. I swear I have this! Supposedly my family doc tested for a gliadin allergy but it was negative. However, I had gone gluten-free for two weeks before the blood test and then only a couple days before the test I started eating gluten again. So, maybe I didn't have enough in my system to show up?? On the other hand, my doc said it's probably IBS, so I'm starting to think they don't take me seriously.

I'm so incredibly frustrated.

My son, with whom I was pregnant when my symptoms started, had an "allergy" to grains the first year of his life. Everytime he ate a piece of bread or cracker, pasta, etc., he would break out on his face in a terrible rash. I took him off gluten and it went away. I then kept testing, periodically giving him a piece of bread, and -whatdoyaknow- his rash came back. After around his first birthday, however, his rash never came back and now he can eat gluten without getting a rash.

Anyway, what you do all think??? I'm starting to get really depressed, angry and desperate!!! I want to go off gluten but I really want to know what it is. It's bothering me. I especially want to know so that, in case I do have celiac, I can get my kids tested. They're so little I want them to be healthy. I think my daughter might be sensitive too.

Thanks a lot for your help.

Kerri


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ravenwoodglass Mentor

I think you should get the full celiac panel run when you see the doctor on Monday. But do remember that there are false negatives. The doctors advice to do an elimination diet was really a good one, it is too bad he didn't refer you to someone or give you some guidance himself. If you don't want another endoscopic exam for biopsies then do just go ahead and give the diet a good strict try. Do you have a copy of the report from your endoscopy that you already had? Sometimes there are changes, like gastritis, certain changes in the mucosal lining, elevations in certain cells that can be seen that are common to celiac but not always diagnostic or recognized as being celiac related. When you are ready to start the diet you have come to the right place for info. There is a lot more to it than just food so feel free to ask any question you need to.

ShayFL Enthusiast

Kerri...you need a complete Celiac panel run and you need to have been eating gluten in fair amounts daily for a good 3 months before the test. Otherwise there is a strong risk of a false NEG. Then you will need another biopsy to take samples specifically for Celiac. This is the only way to get an official dx for Celiac.

If you dont want to do that, then you can pay out of pocket for Enterolab to test for gluten sensitivity and get the genetic testing to see if you have Celiac genes. This will not dx Celiac, but will tell you if you are intolerant to gluten and if you even have the genes.

Do this first and depending on your results you can move on to your kids.

The other alternative is just to eat a gluten-free diet and be healthy. Same for your kids.

What you decide is entirely up to you.

CarlaB Enthusiast

It sounds like you have something systemic going on. I would test for the whole celiac panel and don't get off gluten until you do. :)

If that isn't it, it can still be a toxin problem .... gluten can be a toxin for many of us who do not have celiac. www.biotoxin.info is a website that talks about toxins - mold, gluten, Lyme Disease.

Also, you might check this out - Open Original Shared Link

Whatever, you do, keep looking until you discover how to fix the problem. :)

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    • Oldturdle
      It is just so sad that health care in the United States has come to this.  Health insurance should be available to everyone, not just the healthy or the rich.  My heart goes out to you.  I would not hesitate to have the test and pay for it myself.  My big concern would be how you could keep the results truly private.  I am sure that ultimately, you could not.  A.I. is getting more and more pervasive, and all data is available somewhere.  I don't know if you could give a fake name, or pay for your test with cash.  I certainly would not disclose any positive results on a private insurance application.  As I understand it, for an official diagnosis, an MD needs to review your labs and make the call.  If you end up in the ER, or some other situation, just request a gluten free diet, and say it is because you feel better when you don't eat gluten.      Hang in there, though.  Medicare is not that far away for you, and it will remove a lot of stress from your health care concerns.  You will even be able to "come out of the closet" about being Celiac!
    • plumbago
      Yes, I've posted a few times about two companies: Request a Test and Ulta Labs. Also, pretty much we can all request any test we want (with the possible exception of the N protein Covid test and I'm sure a couple of others) with Lab Corp (or Pixel by Lab Corp) and Quest. I much prefer Lab Corp for their professionalism, ease of service and having it together administratively, at least in DC. And just so you know, Request a Test uses Lab Corp and Quest anyway, while Ulta Labs uses only Quest. Ulta Labs is cheaper than Request a Test, but I am tired of dealing with Quest, so I don't use them so much.
    • Scott Adams
      PS - I think you meant this site, but I don't believe it has been updated in years: http://glutenfreedrugs.com/ so it is best to use: You can search this site for 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/   
    • trents
      A lot to think about here. Does anyone have any recommendations for third party laboratories that will do full panel celiac screens private pay in the U.S.?
    • Scott Adams
      You don't need an official diagnosis to request a gluten-free diet in either a hospital or nursing home--this can be requested by anyone. The higher costs associated with existing conditions for life insurance is a reality, and regardless of your politics, it could become a reality again for health insurance in the USA. For many this could make health insurance unaffordable, thus, everyone who is undiagnosed should understand such potential consequences before they go the official diagnostic route. As mentioned, once it's on your medical record, it won't go away.
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