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

Strong Positive Gliadin Ab


mela14

Recommended Posts

mela14 Enthusiast

This is my second time posting and could use some help here. I've been sick for about 10 years with so many different health problems. Through the past few years things have gotten really bad. I am constantly sick and complaining of muscle and joint pain.Without getting into the whole nightmare I will say that I have lost a lot of weight and complained of feeling week, malnourshed, achy, extremely fatigued with constant migraines. I also complained of diahrea and foul smelling gas and bowel movements. I always assumed it was viral because of all the flu like sypmtoms that came with it. I was told it was fibromyalgia. I am down to 92 libs at 5'3.5". I have not been able to put on weight. I have been to many doctors and told them that I feel better when I do not eat so they assumed I was anorexic. Many times after eating i get sick and feel like I swallowed poison. I got so bad that I used to moan and cry in my sleep feeling sick..and so bloated that I looked pregnant! Often times this happened after going out to dinner with my husband. I felt toxic! i went to about 4 GI drs and all said IBS . they also sent me to gyns thinking it was endometriois. ( i had 7 surgeries for it!! and no ENDO) anwyay, my question is that recently I flew out of my state to see a dr for chronic fatigue. I brought some blood tests and he said that I showed strong positive for Gliadin Antibodies. He put me on a gluten free diet and sent me to a dietician. I have been keeping a journal and finding that I am intolerant to a few other things too. A few times I accidentally had gluten in something and I was sick for days. Is the Gliadin AB test a reliable one for gluten intolerance? Other gluten blood tests seem to be normal. I think there are 3 different tests that can be done. The gliadin AB came back with a 63......which was very strong positive. So is it safe to say in the presence on my symptoms and this one particular blood test that I should continue on this diet? I don't know who else to go to. Another interesting thing that I learned on line is that over-exposure to gluten can cause this intolerance along with trauma, surgery, etc. Well...yes to all of the above! My dad is a baker and I grew up in an Italian bakery....bread and pastries were always around and we thought nothing to eat them for desert. I now learned that everything he baked was made with High-Gluten Flour! I never even knew what it was! I'm not sure what my next step should be and don't want to go through another endoscopy or colonscopy only to bve told it is IBS. Could it be that years ago when they did those procedure they didn't even bother to test for gluten? I am so confused!

Any insight would be appreciated.

Thanks,

Mel


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



Celiac.com Sponsor (A8-M):



darlindeb25 Collaborator

mel--i think listening to your body is the answer----do you feel much better on a gluten-free diet--you stated that you have found other allergens too----the way i look at it--if you keep eating gluten and feel terrible and when you take the gluten away, you feel better, then the gluten is gone from my life--we do not need gluten in our lives to be healthy--i know many feel you must be doctor diagnosed, but i dont feel that way--i doctored for so many years and never found relief until i went gluten free--but my odds are against me in that respect---my sister and i have had the same symptoms all our lives and she is doctor diagnosed and my father just recently was too--so the odds are very strong that i am celiac or at the very least gluten intolerant--i will never go back to a gluten lifestyle--i listen to this old body of mine ;) deb

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,685
    • Most Online (within 30 mins)
      7,748

    Janahawk
    Newest Member
    Janahawk
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.3k

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Thanks for the additional information. I was thinking of asking you if your daughter was taking methylated vitamins since she has the MTHFR gene but you beat me to it. To answer the question you posed in your original post, as I explained, celiac disease does not damage the colon but the lining of the small bowel. If the damage is pronounced enough and the doc doing it is experienced, yes, the damage done to the lining of the small bowel can be spotted with the naked eye.
    • cameo674
      I could not locate the correct Gary Brecka video where he explains the methylation process and specifically states things about how people with the MTRR homozygous gene mutation are known to suffer from heartburn due to a weakened valve/sphincter where the esophagus and the stomach connect.  My brother had the youtube video sent to him from 10x health which is probably why I cannot locate it.     I will have read up on mast cell activation.  I do not know anything about it.  Tums is my preferred gerd treatment.  I always figured a little extra calcium could not hurt me.  
    • cameo674
      Trents: Due to a genetic mutation, my daughter has inherited from both parents she cannot process the Folic Acid provided in the fortified American grains.   An MD told her to avoid eating fortified grains.   My daughter makes the assumption that unless she makes the food item, that the baker used a fortified grain so she has been limiting her gluten intake since 2020.   Her Psychiatrist was who tested her for MTHFR gene issue because she suffers from depression and severe anxiety. The Psychatrist also instructed my daughter to supplement with a methylated version of folate once she knew my daughter was homozygous, because the methylated version bypasses the mutated gene step so her body can absorb it.  Low folate absorption impacts serotonin and dopamine production.  My husband and I also both have two other homozygous gene mutations that interfere with vitamin absorption: MTRR and VDR taq.  The first interferes with B-12 absorption which requires us to take a methylated B-12 vitamin and the second with Vitamin D absorption so we have to take higher doses to stay within normal levels.   My brother, who has the exact same gene mutations, went through 10x health genetic testing for vitamin supplements (paid by his employer) and received a huge report saying the same things about which types of supplements had to be taken.  Gary Brecka does videos on how these gene mutations impact the vitamin absorption pathways.       If my brother had not gotten his testing through work, he would never would have started his supplement journey.  His testing is what triggered my getting functional health testing that tested similar biomarkers to his.  Again the celiac testing was an add-on test that I did off the cuff.  
    • trents
      Welcome to the forum, @growlinhard1! If eliminating gluten from your diet makes significant improvement in your symptoms then there are two possibilities. Either you have celiac disease (aka, gluten intolerance) or NCGS (Non Celiac Gluten Sensitivity, aka, gluten sensitivity). The difference is that celiac disease is an autoimmune disorder that creates inflammation and, over time, damages the lining of the small bowel which inhibits nutrient absorption whereas NCGS does not damage the lining of the small bowel. They share many of the same symptoms. At the end of the day, the antidote for both is to abstain from foods that contain wheat, barley or rye, the three gluten-containing grains. Some countries supply stipends and healthcare benefits for those with an official celiac diagnosis. If you live in the USA that does not apply. The main reasons for seeking an official celiac diagnosis are psychological and social. Many people have a hard time not falling off the gluten free bandwagon without an official diagnosis. They find it easy to rationalize it all away as being temporary or due to something else. When you have an official diagnosis, you tend to take gluten-free eating more seriously. Socially, family and friends are more likely to respect and attempt to comply with your need to eat gluten free if you have an official diagnosis of celiac disease. Your physician is more likely to take you seriously as well if you have an official diagnosis because there are typically other health problems that are spinoffs which develop from celiac disease in time. One autoimmune disease invites others. There are no tests for NCGS. Celiac disease must first be ruled out. We do have specific tests for celiac disease. By the way, some experts believe that NCGS can transition into celiac disease. If your endoscopy/biopsy is only a month away, I would encourage you to stick it out and go back on gluten to get an official diagnosis. You still have time to get a valid test result if you start back on gluten now, 10g of gluten daily which is about the amount found in 4-6 slices of wheat bread.
    • BoiseNic
      I have the same problem. No matter what I eat, I seem to get a break out every 1 to 2 months. I do not do oats, citrus fruits, apples, onions and other foods also, as those cause reactions. The only time I have zero problems is when I fast. The only staple grain I have is quinoa, as that doesn't seem to cause me issues. I have linked mine to a microbiome imbalance. I am currently on month 3 of Skinesa. It's supposed to take 3 months before seeing results. I guess we'll see.
×
×
  • Create New...