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

Qusestion About Endo...and Already Gluten Free


Mama of 6

Recommended Posts

Mama of 6 Rookie

I have a endo scheduled for June 11th. I have already been gluten free since May 1st, if I had villia damage would it still show. If not when do I need to go back on gluten to be visible. I really am not wanting to, I live in horrible pain when eating gluten and take a LONG time to detox from it.


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

I do wish doctors would tell people not to stop with gluten until their endos and blood tests for celiac were all done. If you really need the endo you need to immediately get back on gluten and perhaps consider resceduling the endo for July or August. Does that thought curdle your blood? If so listen to your body. Your doctor can still check for other problems if you are already gluten free but not for celiac.

MitziG Enthusiast

Yeah, you are likely to get a false negative now. It takes 3-4 months of heavy gluten consumption to show the damage- even then it is iffy.

Did you have positive bloodwork already? Combined with your obvious symptoms, you really don't need a confirming biopsy, unless your dr insists and you feel you need his word for a diagnosis.

This is why many people give up on the "gluten challenge" and diagnose themselves. Getting sick from gluten means you shouldn't eat it. Period.

Mama of 6 Rookie

I didn't have positive bloodworm it was actually negative...I just happen to be getting the endo for constant nausea. Just was hoping that they were able to see something. However I am not willing to gluten myself for a POSSIBLE diagnoses.

Just a side note my son did have low IgA level. And is now being tested for IGG levels. Just not understanding why his would show and he is only 6 compared to my while life of eating gluten. I am more frustrated than anything, but I am feeling greatful that I found the culprit.

MitziG Enthusiast

I had undx celiac for 30+ years. My blood tests were a weak psotive. Endoscopy showed many years of damage, total villous atrophy.

My daughter (12) had high blood tests, but not as much damage to villi (though still positive)

My son (7) had very high antibodies, total villous atrophy.

I have a THEORY that because my immune system was so wore out from years of gluten onslaught, it could not muster much of a response anymore to make antibodies to gluten- or anything else I was constantly sick with every little bug that came around- now I NEVER get sick!

tom Contributor

Yeah, you are likely to get a false negative now. It takes 3-4 months of heavy gluten consumption to show the damage- even then it is iffy.

...

Any link for that? I've been trying to gather info on gluten challenge durations & qtys, but I've found very little.

IMHO, a challenge of "3-4 months of heavy gluten consumption" is very rare.

People really have gotten positive celiac disease biopsies from just weeks of moderate consumption.

SO many variables of course - for all we know some subjects were only gluten-free for a month, while others were gluten-free for years before a study began.

MitziG Enthusiast

No links, just going by what I have read here many times. Obviously, every person is going to be different, and the OP may show damaged villi still. Or they might do the full gluten challenge and still come up negative. I tend to error on the side of caution. If someone is going to have the procedure done, best to give it the best chance of showing up!


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

I didn't have positive bloodworm it was actually negative...I just happen to be getting the endo for constant nausea. Just was hoping that they were able to see something. However I am not willing to gluten myself for a POSSIBLE diagnoses.

Just a side note my son did have low IgA level. And is now being tested for IGG levels. Just not understanding why his would show and he is only 6 compared to my while life of eating gluten. I am more frustrated than anything, but I am feeling greatful that I found the culprit.

Was your total IgA tested? You may be low also. In my family I was severely ill for many many years and always showed a false negative. Both my children were low positive on testing though they had much milder GI symptoms. Celiac testing really leaves a lot to be desired.

Mama of 6 Rookie

My total IgA wasnt low. I am just really confused, I just got his results from the IgG and they are normal (7.4 units Normal 19 and below) However his IgA was even lower now. Ugh....I don't know where to go from here.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      how much gluten do I need to eat before blood tests?

    2. - trents replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      IBS-D vs Celiac

    3. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      how much gluten do I need to eat before blood tests?

    4. - SilkieFairy posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      IBS-D vs Celiac

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,321
    • Most Online (within 30 mins)
      7,748

    James Minton
    Newest Member
    James Minton
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • catnapt
      oh that's interesting... it's hard to say for sure but it has *seemed* like oats might be causing me some vague issues in the past few months. It's odd that I never really connect specific symptoms to foods, it's more of an all over feeling of unwellness after  eating them.  If it happens a few times after eating the same foods- I cut back or avoid them. for this reason I avoid dairy and eggs.  So far this has worked well for me.  oh, I have some of Bob's Red Mill Mighty Tasty Hot cereal and I love it! it's hard to find but I will be looking for more.  for the next few weeks I'm going to be concentrating on whole fresh fruits and veggies and beans and nuts and seeds. I'll have to find out if grains are truly necessary in our diet. I buy brown rice pasta but only eat that maybe once a month at most. Never liked quinoa. And all the other exotic sounding grains seem to be time consuming to prepare. Something to look at later. I love beans and to me they provide the heft and calories that make me feel full for a lot longer than a big bowl of broccoli or other veggies. I can't even tolerate the plant milks right now.  I have reached out to the endo for guidance regarding calcium intake - she wants me to consume 1000mgs from food daily and I'm not able to get to more than 600mgs right now.  not supposed to use a supplement until after my next round of testing for hyperparathyroidism.   thanks again- you seem to know quite a bit about celiac.  
    • trents
      Welcome to the celiac.com community, @SilkieFairy! You could also have NCGS (Non Celiac Gluten Sensitivity) as opposed to celiac disease. They share many of the same symptoms, especially the GI ones. There is no test for NCGS. Celiac disease must first be ruled out.
    • trents
      Under the circumstances, your decision to have the testing done on day 14 sounds very reasonable. But I think by now you know for certain that you either have celiac disease or NCGS and either way you absolutely need to eliminate gluten from your diet. I don't think you have to have an official diagnosis of celiac disease to leverage gluten free service in hospitals or institutional care and I'm guessing your physician would be willing to grant you a diagnosis of gluten sensitivity (NCGS) even if your celiac testing comes up negative. Also, you need to be aware that oats (even gluten free oats) is a common cross reactor in the celiac community. Oat protein (avenin) is similar to gluten. You might want to look at some other gluten free hot  breakfast cereal alternatives.
    • SilkieFairy
      After the birth of my daughter nearly 6 years ago, my stools changed. They became thin if they happened to be solid (which was rare) but most of the time it was Bristol #6 (very loose and 6-8x a day). I was on various medications and put it down to that. A few years later I went on this strict "fruit and meat" diet where I just ate meat, fruit, and squash vegetables. I noticed my stools were suddenly formed, if a bit narrow. I knew then that the diarrhea was probably food related not medication related. I tried following the fodmap diet but honestly it was just too complicated, I just lived with pooping 8x a day and wondering how I'd ever get and keep a job once my children were in school.  This past December I got my yearly bloodwork and my triglycerides were high. I looked into Dr. William Davis (wheat belly author) and he recommended going off wheat and other grains. This is the first time in my life I was reading labels to make sure there was no wheat. Within 2 weeks, not only were my stools formed and firm but I was only pooping twice a day, beautiful formed Bristol #4.  Dr. Davis allows some legumes, so I went ahead and added red lentils and beans. Nervous that the diarrhea would come back if I had IBS-D. Not only did it not come back, it just made my stools even bigger and beautiful. Still formed just with a lot more width and bulk. I've also been eating a lot of plant food like tofu, mushrooms, bell peppers, hummus etc which I thought was the cause of my diarrhea before and still, my stools are formed. In January I ran a genetics test because I knew you had to have the genes for celiac. The report came back with  DQ 2.2 plus other markers that I guess are necessary in order for it to be possible to have celiac. Apparently DQ 2.2 is the "rarer" kind but based on my report it's genetically possible for me to have celiac.  I know the next step is to bring gluten back so I can get testing but I am just not wanting to do that. After suffering with diarrhea for years I can't bring myself to do it right now. So that is where I am!   
    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
×
×
  • 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.