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

Risk A Gluten-challenge?


allison

Recommended Posts

allison Rookie

Hi everyone,

I'm new here. I was sick for three years (mostly extreme exhaustion, stomach pains, occassional diarrhea, dizziness, nausea) and decided to try eliminating gluten after a doctor SUGGESTED it (nobody but nobody could figure out what was wrong). I felt much better about a month after the elimination and have been gluten-free since August 2005. Now (and for the last two weeks) I feel like crap again, but I don't think I have been eating differently than usual (maybe a little less careful due to starting a new job and stress?).

The things is that I have never been positively diagnosed because I was in school/traveling and my insurance didn't cover me where I was. Now I'm in NYC and am having an endoscopy on Monday, but I don't think it will really say anything b/c I am gluten-free and have been for a while. (I had the blood tests for antibodies in July and there wasn't any, but it said on the results that they are inconclusive if the person has not been eating gluten.)

So what I'm wondering is: should I risk a gluten challenge? The problem is that I have a job to deal with--and so if I can't go to work, what am i supposed to do? Not a big deal to go to work when you feel sort of bad, but I've been out all this week because I am so dizzy, and my stomach is really bad (especially in the morning, and also with reflux--I think.)

What do you all thing? Has anyone ventured to do this? I can't get a straight answer from anyone on how much gluten I'd have to eat or how long I'd have to eat it before getting a reaction that would be visible in an endoscopy.

Meanwhile, I've eaten only brown rice, boiled chicken, homemade chicken broth, eggs, and minimal amts of gluten-free bread since Tuesday and don't feel any better. SO DIZZY!

Would love to hear what you think--just reading this board is making me feel less depressed--this has been such a long road!

Allison


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

It's a hard call and a personal decision.

I've read four months, the equivalent of four slices per day. I've also read three months and six months. If gluten disables you, that will be VERY long.

Stress can definately contribute to health problems. Google adrenal fatigue and see if it sounds like what you're suffering. It's related to stress.

Our health can be a real puzzle. I'm still working on my puzzle myself

Corkdarrr Enthusiast

As delicious as a gluten challenge sounds some days, I sincerely doubt I would make it.

For me, a postive dietary response was the biggest thing and then I got some testing done through Enterolab just to confirm it for myself.

I've been doing an elimination diet for the past month and feel way better. It's boring and I'm ready to throw a fit if I have to eat stirfry one more night, but obviously something I cut out made me feel a lot better.

Like Carla said, it's a personal decision. But to me, it just wouldn't be worth it.

Courtney

aikiducky Apprentice

How long does your typical gluten reaction last? I ask because mine can sometimes last up to three weeks (not the D necessarily but stuff like bloating, nausea and fatigue). So if you had something a couple weeks ago, maybe ate at a restaurant and got cross contamination on something? It could still explain why you feel bad again right now, but in that case it should pass after a couple more weeks.

I've also heard amounts of time like three months, four or even six, and even then, sometimes people get negative biopsies but feel better gluten free. It's quite a long time to be sick, to confirm something you already know... but it's your decision. :) I should metion that I don't have an official diagnosis for this precise reason so I'm a bit biased. :)

Pauliina

sparkles Contributor

If you have been gluten-free and have been feeling better, I don't think I would risk a gluten challenge. BUT it is a personal decision... I would really consider what the benefit of being glutened on purpose would be! Good luck on your decision.

Creative-Soul Newbie

Whether or not to do a challenge is a very difficult decision to make... for me, I couldn't afford any "official" testing anyway, so I finally decided to attempt one in July as sort of a definitive "diagnosis" for myself...I had been gluten-free for a while and decided that if I experienced any symptoms that would be enough proof for me! After the first day or so I wanted to DIE. A few days later I found myself at my doctor's office (even though I couldn't afford it!) and we had a long talk. He said to stop the challenge immediately seeing that my symptoms were that severe, and that that was enough proof for him as well! So... that's how I was diagnosed...

I think diet alone is a very valid diagnostic tool... Whatever you decide to do, I wish you all the best. All you can do is to make the correct decision for yourself...

Guest cassidy

If you were feeling much better for over a year on the gluten-free diet, then I think that is positive evidence that you need to stay on the diet regardless of what has been going on for the last two weeks.

I can't tell you what has been happening in the last two weeks - you said you may have been less careful. It usually takes me 3 weeks to totally get over a glutening, so even if it happened once, it could still be that. Or, maybe you have another intolerance or some other situaton going on. I just wouldn't think that if the diet made you feel better that it could suddenly not make you feel better anymore. That doesn't make sense to me.

If you have been gluten-free then the biopsy will be negative and I don't see what that will prove. You could always start a gluten challenge and you will probably get very sick and decide to stop doing it. You could always delay the biopsy and see if this temporary problem goes away and then decide what you want to do.

Good luck deciding.


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



Celiac.com Sponsor (A8-M):



hineini Enthusiast

This is a hard one. I tried to go on a gluten-challenge for my blood test because I'd already been gluten-free for 4 months... And I was really excited at the thought of eating all my fave foods again... And BAM, I got so sick I only made it 36 hrs on the challenge! I've been strictly gluten-free since, and have had to accept that this will preclude me from getting a definite diagnosis. I'm learning to live with this, but it's hard. Sometimes it makes me feel a little crazy. I know how sick gluten makes me but I feel that I'm lying when I say "I have celiac disease." My doctors, however, really support me being gluten-free because they've seen how much less sick I am. This really helps.

ajay Newbie
So what I'm wondering is: should I risk a gluten challenge? The problem is that I have a job to deal with--and so if I can't go to work, what am i supposed to do? Not a big deal to go to work when you feel sort of bad, but I've been out all this week because I am so dizzy, and my stomach is really bad (especially in the morning, and also with reflux--I think.)

Hi Allison,

You can search around the boards a bit about testing, because a lot of people wrestle with it. I think part of the question is, do you personally need an official diagnosis? Some people need to have it medically confirmed, for whatever reasons. And if that's what you need, then that's a valid reason. Some figure if you improve on the diet, what more evidence do you need?

Some notes of caution:

1) A positive result is a positive result, but a negative result is a big question mark. There seem to be a lot of people on the boards who officially tested negative but definitely react to gluten. From what you've said, it sounds to me like it would be in your best interest to live gluten free no matter what you get for test results.

2) In my experience (and others have mentioned it, too) after you have gone gluten-free, you may be even more sensitive to gluten than you were before. It's like now your body has enough strength to really react to it. That may be where you are now-- A new job and stress can distract you enough that some small amount of gluten sneaks in and whammo! I used to get big red hives when I ate wheat. I had an accidental challenge this spring. I got a full-on anaphylactic reaction.

There were times when I wanted to get tested for celiac disease since I do get digestive symptoms as well (they just come later). I still wonder if I'm "really" Celiac, but after that last incident, I am firmly in the "not worth it" camp.

I would say the doctor who suggested eliminating gluten should have tested you then... But so many people have problems getting their doctors to even recognize that there's a problem, so I'm *really* glad it even came up as a suggestion. And that you tried it.

Anyway, welcome. Please keep us posted on how you're doing. People here can be very helpful and supportive (and part detective, too).

allison Rookie

Hi everyone!

Your responses are all much appreciated. This has been a very long and difficult road, and I was so SO grateful when I finally felt better that I didn't even want to darken the door of a doctor. The only reason I'm really serious about getting this checked out now is because I'm sick again.

For the record, I don't NEED the official result. Reading on this board, I think I may do a challenge, but only until it makes me sick. Then I'm out. I'll know and accept for sure. And be more careful. I know I must have CCed sometime in the last few months.

Right now, it's obvious that I'm having a major GERD issue (I should have stayed on the prevacid), which will probably show up on Monday in the endoscopy. Other than that, I am SOOOO dizzy, but my stomach has started to feel better and I'm grateful for that too.

I just find it so hard to function when dizzy! Anyone else dealing with this?

Here's another question for you all: something I didn't even connect with gluten before: mouth sores. Have you all had them? What did they look/feel like? I had white BIG ones in the the back of my throat, almost on my tonsils.

Thanks again everyone--this board is a saviour!

Allison

All

Hi Allison,

You can search around the boards a bit about testing, because a lot of people wrestle with it. I think part of the question is, do you personally need an official diagnosis? Some people need to have it medically confirmed, for whatever reasons. And if that's what you need, then that's a valid reason. Some figure if you improve on the diet, what more evidence do you need?

Some notes of caution:

1) A positive result is a positive result, but a negative result is a big question mark. There seem to be a lot of people on the boards who officially tested negative but definitely react to gluten. From what you've said, it sounds to me like it would be in your best interest to live gluten free no matter what you get for test results.

2) In my experience (and others have mentioned it, too) after you have gone gluten-free, you may be even more sensitive to gluten than you were before. It's like now your body has enough strength to really react to it. That may be where you are now-- A new job and stress can distract you enough that some small amount of gluten sneaks in and whammo! I used to get big red hives when I ate wheat. I had an accidental challenge this spring. I got a full-on anaphylactic reaction.

There were times when I wanted to get tested for celiac disease since I do get digestive symptoms as well (they just come later). I still wonder if I'm "really" Celiac, but after that last incident, I am firmly in the "not worth it" camp.

I would say the doctor who suggested eliminating gluten should have tested you then... But so many people have problems getting their doctors to even recognize that there's a problem, so I'm *really* glad it even came up as a suggestion. And that you tried it.

Anyway, welcome. Please keep us posted on how you're doing. People here can be very helpful and supportive (and part detective, too).

key Contributor

I tried to eat gluten for a challenge, but only lasted like 2 days. I was sick as a dog! It was miserable and so I have never made it through one.

My guess is that you are getting gluten contamination from somewhere else. I don't know about the dizziness. You may want to ask in a separate topic about that. I had that once in College and don't know if it was related to undiagnosed celiac disease, but it was horrible.

As far as the reflux, there are quite a few of us having that right now too. I am not really sure what else is causing mine or if I have gotten gluttened from somewhere. THe endoscopy will help see where you are at anyway.

Goodluck and hope you feel better soon.

Monica

Have you had a flu shot? Just curious, because I have heard of a few people having dizziness after that. I had two relatives that had it for awhile. I also had had an MMR vaccine when I suffered dizziness in college. Mine lasted for 6 months. I do vaccinate my kids, but still worry about possible side effects, but they have been ok, so far.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    2. - tiffanygosci posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Aldi Pueblo Lindo Yellow Corn Tortillas

    3. - tiffanygosci replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    4. - trents replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    5. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,977
    • Most Online (within 30 mins)
      7,748

    Riley.
    Newest Member
    Riley.
    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

    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
    • tiffanygosci
      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
    • trents
      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
    • Mari
      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
×
×
  • 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.