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

Gluten Challenge


dfish

Recommended Posts

dfish Apprentice

Hello! I was diagnosed with celiac disease 14 months ago after blood work and have not been very good about following a gluten free diet until recently (within the last month or so). I went to see a gastro because of some other concerns (he is not who originally diagnosed me, that was a general practitioner) and he's concerned about the results of my blood tests not being conclusive for celiac, so he wants me to do a gluten challenge. My next appointment to take blood is in three weeks and to possibly schedule a biopsy at that time. My question is this. I've been eating gluten for a week now since my last doctor's appointment, and I am miserable! If I stop eating gluten again now, is two weeks from my last ingestion a short enough time that my blood work/biopsy will still show some signs of celiac, or do I need to keep eating gluten and being miserable for another two weeks? I was kind of hoping I could get away with a week's worth of gluten and then stopping, especially since I have only truly been gluten free for about a month before starting to eat gluten again.

Thanks so much for your time!!! This disease is so confusing to me and my family and friends that it's great to have a place to ask questions from people who know something about it!

D


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



Celiac.com Sponsor (A8-M):



lovegrov Collaborator

Well, just to frustrate you some more, nobody can tell you how long to eat gluten for certain because it depends on the individual. Most experts would say that if you've been strictly gluten-free for a while you need to eat gluten for three months. Yes, three months.

The fact that you've improved on the gluten-free diet and and are feeling much sicker eating gluten is some evidence in itself. Are you satisfied you have it based on your reaction? What about the tests was "not conclusive?"

richard

KaitiUSA Enthusiast

3 months is usually how long they tell you to be on gluten to have a positive biopsy and blood results. I know people that have done it in 3 weeks but that varies from person to person and for some people that is too short of a time. Did you have positive blood tests 14 months ago? If you had the positive results then why do you need them now?

dfish Apprentice

Richard:

I wasn't actually feeling much better off of the gluten (which is part of the reason why I went back to gastro doctor). I was still having pretty bad diarrhea and stomach pains, and began having major heartburn, which is why I went to the GI doctor (I wasn't able to sleep because of the severity of the heartburn). The tests I had done previously only came back positive for IGG, not for IGA or anti endomysial antibodies. The doctor said that there's a number of things that can cause a positive IGG and that without the positive IGA or anti endomysial antibodies, it's not a conclusive diagnosis of celiac disease. Is that true? I don't know anything about this. Some information I've read online has said that my symptoms could even be caused by endometriosis! Ack! I know that I can pinpoint the date (to the date) that my stomach problems began over a year ago and that going gluten free has not been "revolutionary", I guess, in terms of helping my symptoms and has, in fact, made some things worse (like heartburn), but now I just feel MORE miserable than I felt before since I started eating gluten last week. I have also cut out caffeine, carbonation, fried foods, red meat, and dairy this last week thinking that I could at least isolate some stuff if I started feeling better even though I was eating gluten. Still feel, no pun intended, like poop. :)

Is the info about the tests the doctor said true? Do I even need to bother with this challenge stuff?

KaitiUSA Enthusiast

If you were not doing good on the whole diet and still eating gluten that could be why you were not feeling better. You are not going to get better while you are still on gluten if you are in fact a celiac. It took me 3 months of being gluten free completely to feel about 85% better and longer then that to get back to normal. So it would not happen overnight. My first blood test 2 of the 3 things came back positive and the IGA negative then I got a celiac test done by a reliable celiac testing lab and that test was able to prove I had celiac.

If you have only been completely gluten-free for the past month that might not have been enough time for your body to heal. For some people it takes months and for some it doesn't take long. Also, at first when I started going gluten free there was so many things I thought were gluten free that turned out not to be so there could still be some things slipping into your diet. I hope you start to feel better :D

jknnej Collaborator

I agree with Kati; if you're not 100% gluten-free it could be why you don't feel better. Honestly, once you start eliminating gluten your body gets really angry when a little slips in. I would even venture to say it makes you worse off than you were before.

I also think the first 3 months of gluten-free diet are just as miserable as being on gluten. I am at the tail end of it and starting to feel better but my body went through some serious withdrawl symptoms. They are finally starting to subside, so I say hang in there.

If you pass the three months Absolutely, for sure gluten-free, then check to see what else it could be. I put that last because most of us, by the time we realize we have celiac disease, have already had all of those other tests!!!!

lovegrov Collaborator

I would agree that just a positive Igg isn't an absolute diagnosis (although I do know people who had a positive biopsy after just a positive Igg). Of course I don't know if you have celiac disease, but if you never really followed the diet very well, then there's absolutely no way for you to know if going gluten-free would help or not. Until you go COMPLETELY gluten-free and stay that way for an extended period (more than a month), you can't tell if the diet's helping you. If you DO have celiac disease and you're slipping or cheating frequently, you will continue to fail to improve.

richard


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



Celiac.com Sponsor (A8-M):



Guest BellyTimber

I would say the same as I said in my reply to one of our other correspondents under this topic area, go accompanied, I have had my nose in books on the subject continuously for years (gluten-free diet, not necessarily celiac disease), groups on the subject, kept in touch with individuals doing the same, nutritionist from the Institute of Optimum Nutrition.

To be honest yours is the exact question in my mind when I joined the bulletin board hours ago and I 'm working my way through replying as I go.

I know the answer is, they must take a hike but then I shan't have a plausible prospect of a diagnosis for my job absences. I thought we only have this problem in the UK but it seems doctors are the same the world over.

Thanks so much for daring to post, our Inner Man guides us well...

Best wishes.

Michael

Guest BellyTimber

Another thing - if you were diagnosed has this person any business undiagnosing you?

Come to think of it that has been done to me several times as well.

M.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,964
    • Most Online (within 30 mins)
      7,748

    Cbear
    Newest Member
    Cbear
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.