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

Need Advice Please :)


JessicaB

Recommended Posts

JessicaB Explorer

ok. I would like to know everyones point of view on my stance. I had the blood test for celiac done on 11/15/2005. Here were the levels, IGA 1 (should be 0-4) igg 74 (should be 0-9)ttg iga 0, ttg igg 2 (should be 0-5), endomysial antibody iga 68l (should be 70-400). The doctor said usually two of the first numbers should be high for celiac but since my antibodies were low, thats why only one was high, DOES THAT MAKE SENCE???

Well.....He said the 74 is very high, most likely is has to be celiac. I recieved my biopsy results today THEY ARE NEGATIVE......!! Why???? If im in so much pain when i eat gluten why is there no damage? This has been going on since i had my daughter in july 2004??

Im going to see a specialist at the University of Maryland, Center for Celiac Research, anyone heard of that??

DOES ANYONE KNOW ABOUT THESE LEVELS???? PLEASE LET ME KNOW ASAP I WOULD LIKE TO KNOW YOUR POINT OF VIEWS. DO I HAVE CELIAC?? WHY IS THE BIOPSY NEGATIVE, I KNOW THE SPECIALIST WILL TELL ME BUT I NEED YOUR POINT OF VIEW, OF COARSE, EVERYONE HERE HAS THE EXPERIENCE AND KNOWLEDGE, THANKS A BUNCH!


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



Celiac.com Sponsor (A8-M):



jknnej Collaborator

Hi Jessica,

I can't tell you too much about the tests, but I can tell you that my situation was almost exactly like your own. I only had one high test and the others were normal plus a negative biospy. But, some of the people on the board have said to me that if any of my blood levels were high, I at the very least have gluten intolerance. According to what you said, I doubt a specialist will make very much difference. I have seen one and I didin't get a sure answer.

According to my doctor, I do not have Celiac disease because of the biopsy. He says I have a 50% chance according to the blood work and that I don't have to be gluten free because that is not enough evidence. That is because only one of my tests was high and the biopsy was negative. If you have the same situation you will probably hear the same thing. He is a specialist and knows a lot about celiac disease. He did give me the following advice though:

since I was always sick before going gluten-free it can't hurt to try the gluten-free diet. I am better now after going gluten-free. I have been gluten-free for a year now. I personally know that regardless of whether I have celiac disease or not I need to be gluten free because I am not sick anymore. After all this, he agrees with me and thinks I probably have at the very least gluten intolerance and possibly celiac disease even though there wasn't any damage. He is VERY schooled in celiac disease and as soon as my biopsy was done he was telling me that there are even histiological signs that he can see with the naked eye in most of his Celiac patients that were not present in me, nor were the lab results positive.

Your situation may be a lot different. I can tell you, though, that a biopsy is considered the "gold standard" test for celiac disease and if that came back negative they probably will not diagnose you with celiac disease. You can, though, try going gluten-free to see if you feel better on the diet. If you do, great! If not, maybe there is something else going on in your body.

I haven't had stomach issues in a year (except that i am lactose intolerant and from time to time I divulge in ice cream! ) I get a tummy ache then but it's my own fault and not gluten related!!

So, I would say since you already had the biopsy, try going gluten-free and see if your symptoms get better. It does take time for some, though, and for others they feel better right away.

Good luck!!!!!

JessicaB Explorer

cool, so you saw him also. Yeah ever since i gave birth to my daughter i have had really bad abdominal pain. I went to like 6 different doctors, i have been xrayed, and tested for just about everything, i just want answers ya know. I mean i cant complain that much because the only symptoms i have is pain, depression, mood swings, and bloating. But the bloodtest came out high so i dont know. Thank you for replying to my post. It really helps to know what others have gone through and their similar experiences. Thanks again, and i hope we can keep in touch!

jknnej Collaborator

No problem...there are so many other posters here who are more knowledgeable about the science than I am; however, I think a gluten-free diet can't hurt you since you've already had a biopsy. Normally the only reason NOT to try gluten-free is if you have an upcoming biopsy; then being gluten-free can give you a false negative. But if you were consuming gluten when you had your test than you are safe.

I would try the diet and see if it helps your abdominal pain. The symptoms certainly sound familiar and if you've already been tested for many other things it sounds like it can't hurt to try!

Keep in touch..we're always here!!!! for those of us who are gluten-free this board is like our lifeline!

gabby Enthusiast

The Maryland Celiac center is a top knotch facility....I've been thinking of going there myself. They are not just treating people, but they also do leading edge research. If you can remember...please post here about your experience with them, because I'd love to know if they are more helpful for you (note: I live in Canada, and want to know if it is worth the time and money to make a trip down!)

As for having a negative biopsy....here's what I know. Medicine is not an exact science, there is actually quite a bit of art to it. You can only get so much info from tests, and the rest has to come from putting all the pieces of the puzzle together. You wouldn't believe how many people are sitting in wheelchairs with multiple sclerosis, but all the MS tests come back negative (15% of them actually). Have you heard of women who are 7 months pregnant getting blood tests that say they are not pregnant? etc. The point is that there are always exceptions to the rule...and you could be one of them. A biopsy is a funny thing, because the doctors don't test your entire intestines. They take little pieces from a few parts...but they might miss the damaged sections.

The other possibility is that your intestines are not yet damaged permanently...maybe they are in the process of getting damaged, but your body is strong enough to heal itself for now. I'd wait until the Maryland visit before going too crazy. Tell them your fears, ask them for their recommendations.

All the best to you. I really feel for you, and want you to know that what is happening to you is not as unusual as the medical community wants you to think.

JessicaB Explorer

I had a excellent experience at the University of Maryland today. I would highly reccomment Dr. Fesano, i think i spelled that wrong, sorry. Anyhow, since my bloodwork was high and biopsy negative i brought a copy of all my recent exams and tests with me, it was a full panel. The doctor asked me many questions and did a short exam. After about an hour or so we talked about what needs to be done. He needs to see the biopsy slide himself to determine if any damage has been done. He said sometimes a specialist should look at it because signs of damage can be easily overlooked normally. So basically i have celiac or a wheat intolerance. He discussed both situations to me and i understand more now than i did reading any website or any books i have looked at. He has a nutritionist that works with him, she talked to me, gave me samples of some gluten-free foods, and a free gluten-free cook book. It was great. Lets just hope that i just have wheat tolerance. Ill prob find out the end of next week. He told me that i should stay on the diet no matter which one it is of coarse, since i already feel better, since being gluten-free since thursday the 22nd. Has anyone had a similar experience? Well we will see. Oh, i got a sample of ANNIES gluten-free MAC N CHEESE, ITS REALLY GOOD, ESPECIALLY COMPARED TO ALL THE OTHER PASTAS IVE TRIED!!! Thanks for the replies. Email me anytime! mckaylaslove@aol.com

jknnej Collaborator

I'm so happy you got some answers:) Pretty much what I thought; if you have positive blood work you at least have an intolerance.

Annie's mac n cheese is the BEST.


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



Celiac.com Sponsor (A8-M):



JessicaB Explorer

YESSS! THE MAC N CHEESE IS THE BEST gluten-free PRODUCT IVE TRIED SO FAR. I ALSO LIKE THE AMYS RICE CRUST CHEESE PIZZA. I PUT SOME EXTRA PIZZA CHEESE AND PEPPERONIS ON IT, AND IT WAS REAL GOOD. WHATS SOME OF YOUR OTHER FAVORITES??

YEAH SO EITHER WAY IF I JUST HAVE AN INTOLERANCE I WILL STAY gluten-free, I JUST AM ANXIOUS TO FIND OUT. HA I JUST ORDERED A CASE OF THE MAC N CHEESE :)

Lovinglife Rookie

Dear Jessica,

I'm happy to hear that you've managed to get some answers. YES, be gluten-free/wheat-free as necessary. Take care of yourself.

Love,

Florence

  • 2 weeks later...
Jake Newbie
I had a excellent experience at the University of Maryland today. I would highly reccomment Dr. Fesano, i think i spelled that wrong, sorry. Anyhow, since my bloodwork was high and biopsy negative i brought a copy of all my recent exams and tests with me, it was a full panel. The doctor asked me many questions and did a short exam. After about an hour or so we talked about what needs to be done. He needs to see the biopsy slide himself to determine if any damage has been done. He said sometimes a specialist should look at it because signs of damage can be easily overlooked normally. So basically i have celiac or a wheat intolerance. He discussed both situations to me and i understand more now than i did reading any website or any books i have looked at. He has a nutritionist that works with him, she talked to me, gave me samples of some gluten-free foods, and a free gluten-free cook book. It was great. Lets just hope that i just have wheat tolerance. Ill prob find out the end of next week. He told me that i should stay on the diet no matter which one it is of coarse, since i already feel better, since being gluten-free since thursday the 22nd. Has anyone had a similar experience? Well we will see. Oh, i got a sample of ANNIES gluten-free MAC N CHEESE, ITS REALLY GOOD, ESPECIALLY COMPARED TO ALL THE OTHER PASTAS IVE TRIED!!! Thanks for the replies. Email me anytime! mckaylaslove@aol.com
floriter Newbie

:unsure: hi my name is teri

I'm new to this just register today i'm in the process of being dx or should i say dx with celiac I went for endoscopy to r/o gastitis my gi dr had told be she did some biopseys but didn't think any thing of it 3 weeks later rec'd lab slip in mail for iga , gliadin igg/iga,transglut iga, and reticulin iga I am am a nurse and wa curious about the test so i looked them up on the internet and saw they were all for celiac which I next looked up celiac disease I never thought my test would come back pos I still have not had my follow up with my gi its scheduled for next week I have alot of questions I called the office when I saw 3 of my test come back pos the nurse sent me copy of the celiac food list let me tell you this is all quit over whelming since i always considered myself a carbalcoholic I, trying the diet now its only been a week and I think I'm getting some contaminents ?? I'm not sure how serious I need to take this puzzled i

I've found this web site to be helpful but still have alot of ?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,556
    • Most Online (within 30 mins)
      7,748

    Majesticrb
    Newest Member
    Majesticrb
    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.