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

Brand New


Apsaroke

Recommended Posts

Apsaroke Newbie

Hi everyone,

My name is Chris and it appears that I may have Celiac. I have recently completed the GI and the biopsy came back with blunted villi and mucosal duodenitis (sp?). I'm supposed to go in next week for a blood test specifically to test for Celiac.

I have had digestion issues off and on for years my entire life, however it's been within the last 4 years that things started to get escalate including attacks that have sent me to the hospital. The situation has gotten even worse since July of '07 where I am now pretty much not absorbing much of anything that I eat. I've lost a total of 30 pounds and now weigh in at 110 pounds (height is 5'4").

Additionally -- some of the attacks have been so bad that my body goes into overdrive trying to get rid of the "intruder" and it responds as it would with a severe allergic reaction. This sent me to meet with an allergist who has eliminated HAE (angioedema) and the only things that I responded to are Eggs(1), Milk(2), and Beef(3), listed in order of sensitivity along with scores.

I do have a couple of questions and would appreciate any advice.

1 - I'm seeing references here to enterolab. What exactly is that?

2 - Once the nurse from the GI office informed me of the biopsy results and the upcoming bloodwork, I stopped eating gluten. I have been gluton free for 2 days now. But further reading on the internet had me run across a reference that I should be eating a normal gluten diet prior to the blood test. My only issue is that is that today was the first day that I was able to actually eat something that didn't send me into stomach cramps. The pain is intolerable and I'm so weary of it. If this is something that I have to do, then of course I will do it, but I'm wondering if anyone here had stopped ingesting gluton prior to their bloodwork.

My biggest concern right now is the weight loss. While I understand that responses to going gluten free can be very individualistic, I'm hoping for some suggestions on timelines where other people who experienced weight loss might share with me how long it took for their weight to stabilize and then for them to regain weight.

Having this problem and having had it undiagnosed for so long has robbed me of quite a bit, not only due to never feeling well, but also the depression and irritability that I have had which has impacted my quality of life, but also most recently, it has cost me my marriage. I guess that I really need some hope that things do get better.

Thanks in advance for any help.


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



Celiac.com Sponsor (A8-M):



Ursa Major Collaborator

Hi, and welcome to these boards. Your GI has done things backwards. Normally the blood test is done first, and then the biopsy to confirm the diagnosis. If your villi are blunted, and you have the symptoms, you have celiac disease. Especially since you've had a great response to the diet, there is no doubt at all about the diagnosis.

If I was you, I'd keep eating gluten-free and skip the blood test. You already have a firm diagnosis of celiac disease, no more tests needed. Geez, what is it with doctors these days!

It might take some time before you will gain weight, because you can't absorb nutrients due to villi damage. Be patient, things will normalize eventually. But you have been ill for a long time, you won't heal overnight.

Also, if you have tested allergic to milk and eggs, it would be wise to also eliminate those for the time being. I would also include soy in that list, as it can also hinder healing (besides the fact that unfermented soy is unhealthy).

Make sure you get enough protein and healthy fat. And yes, your body needs saturated fat, non-hydrogenated coconut oil is one of the healthiest saturated fats.

Apsaroke Newbie

Thank you for the quick reply, Ursa. It is really appreciated.

The GI procedure was done on the heels of an emergency room visit (the very next morning) so I won't hold hard feelings about the backwards approach. I was just so happy that someone was being very aggressive and serious in trying to find out what was happening.

I'll post-pone the bloodwork until I meet with my primary care physician and talk with her about it. I appreciate the validation you offer for that. Thinking about going back on gluten just for bloodwork and going through that pain again is something that I just really don't want to do.

Also, thank you for the advice on the non-hydrogenated coconut oil. I've added it to my shopping list. Today is the day I go out for my first gluten free grocery shopping trip!

I've also seen references on the internet about working with a dietician. Is this something that a lot of folks do or do most folks just go forward, avoid gluten and have things sort out on their own over time? I meet with my primary care physician on the 24th (whom I absolutely adore!) and I know she'd refer me to a dietician in a heartbeat if I asked for it. I just want to make sure it would actually be helpful or is that something that really wouldn't be worth the expense?

Thank you for your patience with yet another newbie to this. It's very nice to know that there is a network of individuals to help out. Makes it not so lonely and scary. :)

cruelshoes Enthusiast
1 - I'm seeing references here to enterolab. What exactly is that?

2 - Once the nurse from the GI office informed me of the biopsy results and the upcoming bloodwork, I stopped eating gluten. I have been gluton free for 2 days now. But further reading on the internet had me run across a reference that I should be eating a normal gluten diet prior to the blood test. My only issue is that is that today was the first day that I was able to actually eat something that didn't send me into stomach cramps. The pain is intolerable and I'm so weary of it. If this is something that I have to do, then of course I will do it, but I'm wondering if anyone here had stopped ingesting gluton prior to their bloodwork.

Open Original Shared Link is another form of testing that uses a stool sample rather than blood. It is generally used by those who cannot or choose not to go through testing in the traditional bloodwork/biopsy route. Enterolab's results are not diagnostic. It cannot give you a celiac diagnosis. It can only say that you are producing antibodies to gluten. Enterolab's results are not widely accepted by much of mainstream medicine, because Dr. Fine has never published his results in a peer reviewed forum. Since you already have positive results on a biopsy, I would not be inclined to do enerolab testing if I were in your situation. The biopsy is currently considered the "gold standard" for diagnosis.

I had my biopsy before my bloodwork as well. Normally the bloodwork leads the doctor to order the biopsy. That's the reason it is usually the other way around. A few days off of gluten is not going to be enough to skew your results. It's when you start to go longer than a few days that you can run into problems. If I were in your situation, I would get into the lab as soon as possible and have the complete celaic panel done. That will give you a baseline measurement now to monitor your healing against. Celeiac bloodwork should be repeated yearly to monitor compliance and healing. If you get a reading now, you will have something to compare it to with your future bloodwork. However, I will mention that it is not impossible to have negative bloodwork and a positive biopsy. It is still a celiac diagnosis, however. If your bloodwork is negative, I would still avoid gluten.

Hope this helps.

Nancym Enthusiast

I see no reason not to have the blood work done, just remember that 30% of celiac blood testing is negative unless the villi is completely destroyed. If you get an ignorant doctor they might try to convince you that, based on negative blood work, that you don't have celiac disease. A biopsy should be the final word on that.

Apsaroke Newbie

Thank you for the replies everyone. Sorry for the delay..I've been busy de-toxifying the house so to speak and running here and there replenishing the pantry.

I meet with my primary care doctor in the morning and will be discussing everything with her including the advice given here. I'm still gluten-free and I have now been on liquid vitamins for a week which is really starting to help the energy levels. Still hanging around at 110.5 pounds however, but at least I'm no longer losing weight!! :)

I think at this time, the only way I would consider going back on gluten for the blood test would be if I was also provided something for the nausea and pain management. At the end (prior to the emergency GI procedure) working was impossible and I was in the hospital the evening prior to the procedure.

Thanks again to everyone posting here.

happygirl Collaborator

Safe foods: https://www.celiac.com/articles/181/1/Safe-...ents/Page1.html

Unsafe foods: https://www.celiac.com/articles/182/1/Unsaf...ents/Page1.html

companies that won't hide gluten on their labels: Open Original Shared Link

Hope these help in navigating labels.

Other good websites for info:

www.celiacdiseasecenter.columbia.edu

www.celiacdisease.net

www.celiaccenter.org

www.celiaccentral.org


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor
I see no reason not to have the blood work done, just remember that 30% of celiac blood testing is negative unless the villi is completely destroyed. If you get an ignorant doctor they might try to convince you that, based on negative blood work, that you don't have celiac disease. A biopsy should be the final word on that.

Please forgive the correction but up to 30% of us even with total villi destruction will show negative. As one who was in end stage celiac before diagnosis with constant negative blood work I thought it was important to clarify. I agree with the others about the need to stay on the diet regardless of the results of the blood test. The endo was conclusive, you are celiac no matter what the blood tests show. Choosing to do them is up to you, just don't go by the result if it is negative. Dietary response is really the final word and when you combine that with the 'gold standard' of a positive biopsy there really is no doubt.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,914
    • Most Online (within 30 mins)
      7,748

    ChrisMary
    Newest Member
    ChrisMary
    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

    • Clear2me
      All of a sudden I can't get any gluten-free nuts. There are only 2 nuts available that I can find on the market that are gluten-free. One is Mauna loa brand macadamia nuts, the other is Wonderful pistachios. Other than that all types of nuts that are plain nuts, roasted or raw are no longer gluten-free and are processed and plants that also process wheat.  Has anyone found a source for Pecans, almonds peanuts, walnuts, Pine nuts, etc that is gluten-free?
    • knitty kitty
      @Xravith, How are you doing?   Two cookies are not enough.  For testing, you need to be eating a minimum of ten grams of gluten for two weeks minimum before testing for Celiac antibodies.  Ten grams of gluten is roughly five or six slices of gluten containing bread per day for two weeks minimum. Breads that contain lots of gluten typically have large bubbles formed by gases escaping during baking.  Gluten helps form those bubbles of trapped gases, like a balloon.  Artisan breads, and thick, chewy pizza crust are good examples.  Look at the size of the bubbles in cakes and cookies.  Small bubbles, so not lots of gluten in them.  You'd have to eat tons of cookies to get ten grams.   Antibodies are made in the small intestine. If you eat at least TEN grams of gluten for at least two weeks, then there will be sufficient antibodies to move into the bloodstream, which can be measured in antibody tests.   If you eat less than ten grams of gluten daily, you will get celiac symptoms, but not enough antibodies will get into the bloodstream to be measured, resulting in false negatives.  Anemia, diabetes, and thiamine deficiency can also affect testing, resulting in false negatives. Since you are having such difficulty consuming sufficient quantities of gluten, you should consider getting a genetic test done.  You do not have to eat gluten to have a genetic test done.  Celiac is inherited.  It's in your genes.  Genes don't change whether you eat gluten or not.  A genetic test looks for the most common known Celiac genes.  If you do not have the genes, your doctor can look for other health conditions that can be causing symptoms.  If you do have Celiac genes, you can assume that those genes are actively causing symptoms.  An endoscopy to check for the amount of intestinal damage caused by Celiac Disease is usually done.   You should also be checked for nutritional deficiencies.  Ask for an Erythrocyte Transketolace Activity test, which checks for Thiamine deficiency.  Thiamine, Vitamin B 1, is one of the eight essential B vitamins.  Thiamine can become low quickly because our bodies use so much of it everyday.  If we're not replenishing Thiamine daily from our diet or because of malabsorption, we can become seriously ill.  Same with the other seven B vitamins.   Doctors are not familiar with nutritional deficiency symptoms as can occur in Celiac disease.  Please get checked for nutritional deficiencies.  Ask for the Erythrocyte Transketolace Activity test soon. Please let us know how you are doing.  
    • Rogol72
      @klmgarland, My dermatitis herpetiformis didn't clear up until I became meticulous about cross contamination. I cut out gluten-free oats and all gluten-free foods, dairy and gluten-free rice. Additionally, getting the right amount of protein for my body weight helped significantly in my body's healing process ... along with supplementing with enough of all the vitamins and minerals ... especially Zinc and Magnesium. I went from 70kg to 82kg in a year. Protein with each meal 3 times daily, especially eggs at breakfast made the difference. I'm not sure whether iodine was a problem for me, but I can tolerate iodine no problem now. I'm off Dapsone and feel great. Not a sign of an itch. So there is hope. I'm not advocating for the use of Dapsone, but it can bring a huge amount of relief despite it's effect on red blood cells. The itch is so distracting and debilitating. I tried many times to get off it, it wasn't until I implemented the changes above and was consistent that I got off it. Dermatitis Herpetiformis is horrible, I wouldn't wish it on anyone.  
    • klmgarland
      Thank you so very much Scott.  Just having someone understand my situation is so very helpful.  If I have one more family member ask me how my little itchy skin thing is going and can't you just take a pill and it will go away and just a little bit of gluten can't hurt you!!!! I think I will scream!!
    • Scott Adams
      It is difficult to do the detective work of tracking down hidden sources of cross-contamination. The scenarios you described—the kiss, the dish towel, the toaster, the grandbaby's fingers—are all classic ways those with dermatitis herpetiformis might get glutened, and it's a brutal learning curve that the medical world rarely prepares you for. It is difficult to have to deal with such hyper-vigilance. The fact that you have made your entire home environment, from makeup to cleaners, gluten-free is a big achievement, but it's clear the external world and shared spaces remain a minefield. Considering Dapsone is a logical and often necessary step for many with DH to break the cycle of itching and allow the skin to heal while you continue your detective work; it is a powerful tool to give you back your quality of life and sleep. You are not failing; you are fighting an incredibly steep battle. For a more specific direction, connecting with a dedicated celiac support group (online or locally) can be invaluable, as members exchange the most current, real-world tips for avoiding cross-contamination that you simply won't find in a pamphlet. You have already done the hardest part by getting a correct diagnosis. Now, the community can help you navigate the rest. If you have DH you will likely also want to avoid iodine, which is common in seafoods and dairy products, as it can exacerbate symptoms in some people. This article may also be helpful as it offers various ways to relieve the itch:  
×
×
  • 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.