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

1 Week Left Till Endoscopy And Colonoscopy!


Mommabearof3

Recommended Posts

Mommabearof3 Rookie

I can't wait till testing is over. My bloods came back negative, but it turns out they didn't run a full panel so the scope is my last chance for a diagnosis at this point. I don't care even if it comes back negative, the first thing I'm doing is cutting a lot of crap, including gluten, from my diet to try to improve my stomach.

I'm in so much pain today because I'm stopped up, after months of D. I haven't taken anything or changed my diet, so no clue why this is happening now :-(

Liz


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



Celiac.com Sponsor (A8-M):



icelandgirl Proficient

I can't believe they didn't run a full panel...How frustrating! Are you thinking about having the do the rest of the bloodwork? You are doing so great hanging in there with all of this waiting. Please let us know how the biopsy goes.

Mommabearof3 Rookie

It is frustrating. I thought I was waiting for more results to load to my online account, because they were were also suposed to run a free T4 which they apparently didn't.

They only ran three celiac tests (the two deaminated iga and igg ones andthe tissue trans...whatever that long word is...iga) and a total iga. IGA came back at 332, with the range being 66 to 344. So I'm not IGA deficient, but they didn't test total IGG.

I don't even know if I should push for additonal testing or what. I looked at the lab guidelines on tests and they do not offer any other celiac tests but these three. I don't know if it's worth seeking out another doctor or just get the endo done and do the diet anyway.

I don't "need" a diagnosis. As an example, I have a pretty severe gastrointestinal reaction to straight up eggs. Worse then my regular reaction to things I eat. I figured it out on my own, and when asked at doctor appointments or past hospital stays, no one has ever questioned me on it. They just mark my chart as "egg allergy" and we move on. Only one nurse ever asked me what happens when I eat them, I told her about the 4 plus hours I will be in the bathroom and she just said, yeah I'd stay away from them too.

Liz

SMRI Collaborator

The total IgG is less important than the total IgA.  If your TTIgA/IgG's came back negative with a normal IgA, that information is about as accurate as you can get.  Now, if you have symptoms of low IgG, that might be a test to ask for.  Are you sick all the time with colds, pneumonia, bronchitis, severe sinus infections, etc. that need 3 or 4 rounds of antibiotics to clear?  The GI stuff could be low IgG subclass 3 but that portion of the overall IgG is so small that it won't alter the overall IgG level.  I'm assuming they have done food allergy testing?

Mommabearof3 Rookie

Thanks for that info. I have multiple sinus infections, ear infections, severe bronchitis requiring antibiotics, steroids and nebulizer treatments throughout the year. I saw an ent a month ago because I've had multiple ear infections in the last 2 to 3 years after 25 years of none and he said it was caused by allergies but did not offer any testing, just gave me allergy medicine.

I've always had odd occurrences of illness, 2nd grade I had strep throat 8 times in the school year, I'd get better and 5 days later I would have it again.

I also had mono when I was 14 and that completely killed my entire system for years.

Liz

SMRI Collaborator

Thanks for that info. I have multiple sinus infections, ear infections, severe bronchitis requiring antibiotics, steroids and nebulizer treatments throughout the year. I saw an ent a month ago because I've had multiple ear infections in the last 2 to 3 years after 25 years of none and he said it was caused by allergies but did not offer any testing, just gave me allergy medicine.

I've always had odd occurrences of illness, 2nd grade I had strep throat 8 times in the school year, I'd get better and 5 days later I would have it again.

I also had mono when I was 14 and that completely killed my entire system for years.

Liz

 

I would make an appointment with an infectious disease doctor.  Given your Celiac testing came back negative, it's possible with your symptoms that you issues are immune related and not Celiac.  They should test your full IgG as well as the 4 subclasses.  I'm assuming you are old enough to remember the movie "Boy in the Plastic Bubble"  that is the same condition as the immune deficiency, an extreme case of it. With the upper respiratory symptoms, you are probably low IgG subclass 2 and the GI stuff is possibly low subclass 3.  Your overall IgG levels could be, and probably are, "normal" but since subclass 1 is the biggest, you need the subclasses tested as well.  If you were subclass 1 deficient, you would be in the hospital for a couple weeks with most of those above illnesses needing IV antibiotics.  I don't know where you are located but I'll suggest again going to Mayo for a complete work up vs having a test here, a test there and getting to the bottom of your symptoms.

Mommabearof3 Rookie

I would make an appointment with an infectious disease doctor. Given your Celiac testing came back negative, it's possible with your symptoms that you issues are immune related and not Celiac. They should test your full IgG as well as the 4 subclasses. I'm assuming you are old enough to remember the movie "Boy in the Plastic Bubble" that is the same condition as the immune deficiency, an extreme case of it. With the upper respiratory symptoms, you are probably low IgG subclass 2 and the GI stuff is possibly low subclass 3. Your overall IgG levels could be, and probably are, "normal" but since subclass 1 is the biggest, you need the subclasses tested as well. If you were subclass 1 deficient, you would be in the hospital for a couple weeks with most of those above illnesses needing IV antibiotics. I don't know where you are located but I'll suggest again going to Mayo for a complete work up vs having a test here, a test there and getting to the bottom of your symptoms.

Thanks for the info, it looks like I have some stuff to look up so I can understand igg and the immune system more. Yes, I remember the boy in the plastic bubble and I've often joked that I needed to be in one because I catch almost everything. I even had the chicken pox twice because the first time I didn't build up enough of an immunity to it.

I can't afford a trip to the mayo clinic unfortunately. I'LL hopefully know more after my testing Monday and I'm planning on still doing an elimination diet after testing in order to pinpoint what is bothering me.

Liz


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,929
    • Most Online (within 30 mins)
      7,748

    Mike Rowicki
    Newest Member
    Mike Rowicki
    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

    • lehum
      Hi and thank you very much for your detailed response! I am so glad that the protocol worked so well for you and helped you to get your health back on track. I've heard of it helping other people too. One question I have is how did you maintain your weight on this diet? I really rely on nuts and rice to keep me at a steady weight because I tend to lose weight quickly and am having a hard time envisioning how to make it work, especially when not being able to eat things like nuts and avocados. In case you have any input, woud be great to hear it! Friendly greetings.
    • Hmart
      I was not taking any medications previous to this. I was a healthy 49 yo with some mild stomach discomfort. I noticed the onset of tinnitus earlier this year and I had Covid at the end of June. My first ‘flare-up’ with these symptoms was in August and I was eating gluten like normal. I had another flare-up in September and then got an upper endo at the end of September that showed possible celiac. My blood test came a week later. While I didn’t stop eating gluten before I had the blood test, I had cut back on food and gluten both. I had a flare-up with this symptoms after one week of gluten free but wasn’t being crazy careful. Then I had another flare-up this week. I think it might have been caused by Trader Joe’s baked tofu which I didn’t realize had wheat. But I don’t know if these flare-ups are caused by gluten or if there’s something else going on. I am food journaling and tracking all symptoms. I have lost 7 pounds in the last 10 days. 
    • trents
      Welcome to the forum, @Hmart! There are other medical conditions besides celiac disease that can cause villous atrophy as well as some medications and for some people, the dairy protein casein. So, your question is a valid one. Especially in view of the fact that your antibody testing was negative, though there are also some seronegative celiacs. So, do you get reactions every time you consume gluten? If you were to purposely consume a slice of bread would you be certain to develop the symptoms you describe?
    • klmgarland
    • DebJ14
      I only went on the multi vitamin AFTER a couple of year of high dose, targeted supplementation resolved most of my deficiencies.  I was on quite a cocktail of vitamins that was changed every 6 months as my deficiencies resolved.  Those that were determined to be genetic are still addressed with specific doses of those vitamins, minerals and amino acids. I have an update on my husband and his A Fib.  He ended up in the hospital in August 2025 when his A Fib would not convert.  He took the maximum dose of Flecainide allowed within a 24 hour period.  It was a nightmare experience!  They took him into the ER immediately.  They put in a line, drew blood, did an EKG and chest Xray all within minutes.  Never saw another human for 6 hours.  Never got any results, but obviously we could see he was still in A fib by watching the monitor.  They have the family sign up for text alerts at the ER desk.  So glad I did.  That is the only way we found out that he was being admitted.  About an hour after that text someone came to take him to his room on an observation floor.  We were there two hours before we saw another human being and believe it or not that was by zoom on the TV in the room.  It was admissions wanting to know his vaccine status and confirming his insurance, which we provided at the ER desk.  They said someone would be in and finally a nurse arrived.  He was told a hospitalist was in charge of his case.  Finally the NP for the hospitalist showed up and my husband literally blew his stack.  He got so angry and yelled at this poor woman, but it was exactly what he needed to convert himself to sinus rhythm while she was there.  They got an EKG machine and confirmed it.  She told him that they wanted to keep him overnight and would do an echo in the morning and they were concerned about a wound on his leg and wanted to do a doppler to make sure he did not have a DVT.  He agreed.  The echo showed everything fine, just as it was at his annual check up in June and there was no DVT.  A cardiologist finally showed up to discharge him and after reviewing his history said the A Fib was due to the Amoxicillan prescribed for his leg wound.  It both triggers A Fib and prevents the Flecainide from working.  His conversion coincided with the last dose of antibiotic getting out of his system.  So, make sure your PCP understands what antibiotics you can or cannot take if susceptible to A Fib.  This cardiologist (not his regular) wanted him on Metoprolol 25 mg and Pradaxa.  My husband told him that his cardiologist axed the idea of a beta blocker because his heart rate is already low.  Sure enough, it dropped to 42 on the Metoprolol and my husband felt horrible.  The pradaxa gave him a full body rash!  He went back to his cardiologist for follow up and his BP was fine and heart rate in the mid 50's.  He also axed the Pradaxa since my husband has low platelets, bruises easily and gets bloody noses just from Fish Oil  He suggested he take Black Cumin Seed Oil for inflammation.  He discovered that by taking the Black Seed oil, he can eat carbs and not go into A Fib, since it does such a good job of reducing inflammation.   Oh and I forgot to say the hospital bill was over $26,000.  Houston Methodist!  
×
×
  • 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.