Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Orientation


baby.alpaca

Recommended Posts

baby.alpaca Rookie

Hello,

I'm very happy to have found this forum.

I'm a 30 y.o. male. My issues begin about two years back. I was under a lot of work stress at this time and living in areas where food options where limited. I suddenly found my body was getting sick daily. I attributed this to the food I was consuming at the time, small towns where ingredients weren't the best and hygiene wasn't the ideal. I was getting diarrhea with heavy gas daily. At first I tried taking over the counter medicine, but this didn't help much. I started limiting my diet to only fruit, toasted bread and tuna yet I was still getting sick daily. Eventually I ended up going to the town doctor who said I had colitis and that it was caused by stress. 
I remember she gave me some medication and I eventually ended up quitting that work gig because the stress was too much. When I got back home to the city my health improved but there were still some small issues (not as noticeable as before but still there). 
A few months later I had an anal abscess which came very close to extending to other organs and damaged my sphincter about 40% (I only mention this because I've read that celiac disease can sometimes be triggered by surgery). This wasn't my first anal surgery, as I had already had an anal fissure about a year prior. 
Once the anal abscess healed I had another surgery to help correct my sphincter but the result wasn't what we expected. I ended up doing hyperbaric chamber to help my wound heal. 
This entire process caused me a great deal of stress. Due to the damage to my sphincter I had a small level of gas incontinence which caused even more stress.
The diarrhea and gas problems where still very present. I was depressed and didn't understand why I was getting sick daily. My proctologist told me to visit a gastroenterologist he recommended. He said before we continue working on my sphincter we have to find out what is causing these issues. The gastro. had me do some some test on a sample of my excrement. When she saw the results she said everything looked ok except for the level of mucus. She said I should have a colonoscopy. I did, and they took a biopsy. Results showed that the small fibers that absorb the nutrients where damaged and almost completely gone and that there was some type of colitis present (I forget the name). She then said I had to have blood tests because this might be celiac disease. She said it wasn't chrons or cancer.
I just had the tests done two days ago and results will be ready until the 22nd of this month.

Now, I've written all this just to ask.... since I've already had the blood tests (I made sure to consume gluten daily prior to my blood tests) and I've already had the colonoscopy and biopsy. Do you think I'd be okay if I started a gluten free diet from now? 

From what I gather from my doctor, based on the colonoscopy and biopsy results she's pretty sure it could be celiac disease but she just needs the blood tests to confirm.

Thank you for your time!

 


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

Hi,

You need to be eating gluten daily for 8 to 12 weeks before the blood tests.  And be eating  gluten for 2 weeks before the endoscopy.  If this didn't happen, your test results may not be valid.

I suggest you cut down eating gluten to a minimal amount for now,  Don't stop entirely until the Dr, appointment and test verification.  You'll need to decide if you are going to follow the gluten-free diet regardless of the test results.  I suggest you decide to go gluten-free for 1 year and see how it affects your health regardless of test results.  Our bodies are pretty good about letting us know what they don't like if we listen.

trents Grand Master

Welcome to he forum, baby.alpaca!

I'm a little confused by your post. Doctors don't use a colonoscopy to diagnose celiac disease. They use an "endoscopy." A colonoscopy examines the lower intestinal track below the area that is directly affected by celiac disease. Celiac disease directly affects the small bowel, the area just below the stomach. It damages the mucosa of the small bowel which is where the nutrients in our food are absorbed. Specifically, it blunts the "villi," the small, finger like projections of the mucosal lining that provide the abundant surface area for nutrient absorption. Celiac disease is classified as an autoimmune disease and one that is triggered by the ingestion of the gluten found in wheat, barely, rye and (for about 10% of celiacs) oats. 

A colonoscopy cannot reach up far enough to examine and biopsy the small bowel so they run the scope down through the mouth, throat, stomach and into the small bowel. So my question is, has your doctor scheduled an endoscopy for you yet? If so, you should continue eating the equivalent of 1-2 slices of wheat bread per day until the scoping is done. If your gastro has already done the blood tests specific for celiac disease, and they are positive, he (or she) may or may not want to do an endoscopy. If you can gut it out (excuse the pun), I would continue to consume some gluten until you find out whether or not your doctor wants an endoscopy done. You can cut back on gluten but continue to eat 1 or 2 slices of wheat bread worth of gluten daily to prevent healing of the mucosa. On the other hand, if the blood tests are positive for celiac disease you may opt to forego the endoscopy/biopsy of the small bowel and just assume you have celiac disease. 

Historically, the endoscopy/biopsy of the small bowel has been the gold standard for confirming celiac disease but there is a recent tendency for doctors to forego it if the blood tests are strongly positive. 

Having said all that, other bowel diseases such as Crohn's and ulcerative colitis are experienced by celiacs in higher numbers than with the general population. In fact, there is a higher incidence of many autoimmune diseases in the celiac population than in the general population.

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,382
    • Most Online (within 30 mins)
      7,748

    victimm
    Newest Member
    victimm
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • lauramac
      I was diagnosed with Celiac Disease abput 10 years ago. When I was initially diagnosed my only "symptom" was persistently low iron (that occasionally dipped into anemia). After diagnosis,  over time, I started to develop symptoms when exposed to gluten--they have been overall relatively minor, but have increased over time (and yes, I realize my guts are likely being wrecked regardless of the symptoms) on the rare occasions I've been exposed to gluten. I had COVID19 last week (now testing negative) and was glutened last night (never trust anything labeled gluten-free in a mixed environment). I had my traditional symptoms (sharp gas pains, burping, nausea, stomach ache) but they were accompanied by new, more intense symptoms (muscle cramps all over my body--feet, calves, biceps, neck, shoulders, jaw, abdomen, I'm still sore today and cold sweats). I spent about 6 hours writhing before I felt well enough to get up.  I have been told by my allergist that COVID19 can cause your immune system to hyper react. I'm wondering if that's what happened here.   Has anyone else had experience getting glutened post COVID19? Relatively shortly after recovering from COVID19? Was it a more extreme reaction or same? I can't seem to find any articles on this, so I thought I'd ask the community.  Thank you!
    • Rogol72
      A friend of mine is in the bar trade most of his life and has never heard of lines being mixed for different type of beers and ciders. Better to stick with cans.
    • Rejoicephd
      Thanks very much for confirming my suspicion @Scott Adams! That helps a lot because I'm really trying to track down and get rid of these sources of cross-contact and so I'm going to just rule out the draft ciders and hope that helps. Also @Rogol72 its nice to hear you haven't had a problem on that side of the pond - draft cider lines being used for cider only certainly sounds like the right way to do it, but I think that must not always be practiced over here! 
    • Zuma888
      I didn't ask a doctor about this actually. I did ask several doctors a long time ago and they told me gluten has nothing to do with hashimoto's. One of them told me to do a gluten challenge to test for celiac, but at the time I was in graduate school so couldn't afford to be even more ill than I was. If you have the symptoms, I really don't advise you to do a gluten challenge. It messed me up mentally and physically for months. At the same time, I benefitted from doing the challenge in the sense that it convinced me that all my symptoms were truly from gluten - even stuff like insomnia! So now I am terrified to eat gluten, whereas before I would have a little once in a while and not notice anything dramatic. 
    • Winnie-Ther-Pooh
      I am in a similar situation where I can't feasibly do a gluten challenge but have all the symptoms and I have 2 celiac genes. I'm curious if your doctor advised you to eat as if you had a diagnosis or if they were more dismissive about it. 
×
×
  • Create New...