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

Blood Test Positive...biopsy Negative.


MollyBrack

Recommended Posts

MollyBrack Newbie

Two years ago I was diagnosed via bloodwork as having Celiac. Here are the results from that test:

Gliadin IgA Ab 32 0 - 19 Units H Tissue Transglut Ab IgA 98 0 - 19 Units H

 

Last week I was hospitalized for gallbladder surgery and an upper GI series of tests were done including a biopsy testing for Celiac which came back negative. 

 

One GI doc said that the blood test is 100% reliable and no biopsy was necessary.

The doc who did the endoscopy said that the blood work is completely unreliable and only a biopsy will tell the truth.

P.S. Both docs said "it's just an allergy...you can eat bread once in a while, just don't over-do it"

 

Now what??

 

Have I gone two years without croissants for NOTHING???

;)

 

 


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



Celiac.com Sponsor (A8-M):



psawyer Proficient

Hi,

 

You were diagnosed two years ago. If you have been following a gluten-free diet for two years, it is quite likely that your villi have healed, and will give a negative biopsy result. Likewise, a blood test today would not find antibodies, because you don't make them without gluten, and that's why your villi can heal.

 

I showed a strong positive on a biopsy in 2000. A repeat procedure a few years later showed no abnormalities. It didn't mean I don't have celiac disease; it meant that my adherence to the diet was successful, and my intestines had healed.

 

A competent gastroenterologist should know that.

 

:(

bartfull Rising Star

If you've been gluten-free for 2 years you will test negative on the blood tests and the biopsy. Your doctor should KNOW that. And both of them should know that you CAN'T eat a little bread once in a while. They are both idiots, IMO!

MollyBrack Newbie

Yes, this makes sense to me. I read up a bit more and understand why the biopsy could be negative either way. 

 

And yes, it is alarming that both of the GI "specialists" I've seen, my GP and my rheumatologist ALL have said that Celiac disease is "just an allergy". 

notme Experienced

they should give them all celiac 'connect the dots' workbooks - if you have rheumatoid arthritis, that is also related to celiac.  i guess they all lose $$ if they don't treat you for one *symptom* at a time..........  and eating bread once in awhile will keep you sick enough to keep going to the doctor:  job security!  if you eat enough gluten, i guess you can keep all sorts of doctors in business :(

w8in4dave Community Regular

Wow!! Thats crazy!! I mean I read all over that you have to be eating Gluten for a while to be tested positive. Why would they tell you that? That is some crazy stuff right there!! So have you felt better after your two years Gluten Free? 

MollyBrack Newbie

I just got  a letter from the GI practice congratulating me on being celiac free. I brought up the thing about negative results because I've been off gluten to my GP and she dismissed it as "internet stuff". 

 

So, who do you believe...four people who have been to medical school or a hundred different websites that contradict them? The one site that I think gives some credibility is www.uptodate.com which is the one many doctors use when researching a diagnosis. It is the latest information from medical journals and research outcomes. You have to be a doctor to see the whole site but consumers can see parts of it. My rheumatologist showed me the section on celiac where it CLEARLY says that it is NOT an allergy but an auto-immune disorder. Then he told me it's really an allergy and I should have birthday cake if I want it.

 

Dave -- I wish I could say that I feel a lot better off of gluten, but really only a couple of my symptoms have improved (headaches and brain fog). I do have rheumatoid arthritis so many other symptoms are the same - joint pain, fatigue, etc. It's sometimes hard to tell if being gluten-free has helped, but I think that it has and I intend to remain so. Although, I have to say I experimented with a giant chocolate eclair one day just to see what would happen and  what happened was...nothing. But other times I've gotten a little soy sauce and been sick immediately.

 

It's all very confusing and frustrating not to feel confident in my diagnosis and treatment, and to have my doctors all poo-pooing the whole thing. But I gather from reading various forums that this is a common situation and that many healthcare professionals still don't really understand Celiac disease. 


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Open Original Shared Link

Why not believe people with a medical degree who are experts in celiac Disease?

w8in4dave Community Regular

I just got  a letter from the GI practice congratulating me on being celiac free. I brought up the thing about negative results because I've been off gluten to my GP and she dismissed it as "internet stuff". 

 

So, who do you believe...four people who have been to medical school or a hundred different websites that contradict them? The one site that I think gives some credibility is www.uptodate.com which is the one many doctors use when researching a diagnosis. It is the latest information from medical journals and research outcomes. You have to be a doctor to see the whole site but consumers can see parts of it. My rheumatologist showed me the section on celiac where it CLEARLY says that it is NOT an allergy but an auto-immune disorder. Then he told me it's really an allergy and I should have birthday cake if I want it.

 

Dave -- I wish I could say that I feel a lot better off of gluten, but really only a couple of my symptoms have improved (headaches and brain fog). I do have rheumatoid arthritis so many other symptoms are the same - joint pain, fatigue, etc. It's sometimes hard to tell if being gluten-free has helped, but I think that it has and I intend to remain so. Although, I have to say I experimented with a giant chocolate eclair one day just to see what would happen and  what happened was...nothing. But other times I've gotten a little soy sauce and been sick immediately.

 

It's all very confusing and frustrating not to feel confident in my diagnosis and treatment, and to have my doctors all poo-pooing the whole thing. But I gather from reading various forums that this is a common situation and that many healthcare professionals still don't really understand Celiac disease. 

 

Sorry to hear after 2 years your really not feeling any better. Wish there was something magical I could say. But there isn't. I am going to pop into that site you posted. Good luck to you I hope you find the answer you need.

0range Apprentice

Many doctors are very deficient in their knowledge about autoimmune disorders, not just celiac. Hasn't it been uniformly agreed upon that it isn't an allergy or an intolerance? Strikes me as so odd that specialists would not know this.

Mum in Norway Contributor

I study nutrition, and last fall we had a course on diseases. This was only very basic, but even there we learnd that 'celiac is an autoimmune disease that is triggerd by consuming gluten. Gluten will then caus the body to attack the small intestine, resulting in a flattening of the villi. Only cure is being glutenfree for life, and after some time of being glutenfree the intestine will heal and there will be no sign of the disease.'.

 

Thats about all it said about celiac, but it seems to be more than many docs' know! How can that possibly be?

nora-n Rookie

of course the biopsy will be negative after a while off gluten!!

 

Where was that?

Do they really tell patients their celiac went away?

bartfull Rising Star

You should contact the AMA and let them know what these doctors  are telling patients. They should be stipped of their licenses to practise!

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. - SilkieFairy replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      IBS-D vs Celiac

    2. - par18 replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      IBS-D vs Celiac

    3. - trents replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      IBS-D vs Celiac

    4. - SilkieFairy replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      IBS-D vs Celiac

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

    • Total Members
      133,339
    • Most Online (within 30 mins)
      7,748

    Teresa King
    Newest Member
    Teresa King
    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

    • SilkieFairy
      I realized it is actually important to get an official diagnosis because then insurance can cover bone density testing and other lab work to see if any further damage has been done because of it. Also, if hospitalized for whatever reason, I have the right to gluten-free food if I am officially celiac. I guess it gives me some legal protections. Plus, I have 4 kids, and I really want to know. If I really do have it then they may have increased risk. 
    • par18
      Been off this forum for years. Is it that important that you get an official diagnosis of something? It appears like you had a trigger (wheat, gluten, whatever) and removing it has resolved your symptom. I can't speak for you, but I had known what my trigger was (gluten) years before my diagnosis I would just stay gluten-free and get on with my symptom free condition. I was diagnosed over 20 years ago and have been symptom free only excluding wheat, rye and barley. I tolerate all naturally gluten free whole foods including things like beans which actually helps to form the stools. 
    • trents
      No coincidence. Recent revisions to gluten challenge guidelines call for the daily consumption of at least 10g of gluten (about the amount in 4-6 slices of wheat bread) for a minimum of 3 weeks. If possible, I would extend that two weeks to ensure valid testing.
    • SilkieFairy
      Thank you both for the replies. I decided to bring back gluten so I can do the blood test. Today is Day #2 of the Challenge. Yesterday I had about 3 slices of whole wheat bread and I woke up with urgent diarrhea this morning. It was orange, sandy and had the distinctive smell that I did not have when I was briefly gluten free. I don't know if it's a coincidence, but the brain fog is back and I feel very tired.   
    • knitty kitty
      @Jane02, I hear you about the kale and collard greens.  I don't do dairy and must eat green leafies, too, to get sufficient calcium.  I must be very careful because some calcium supplements are made from ground up crustacean shells.  When I was deficient in Vitamin D, I took high doses of Vitamin D to correct the deficiency quickly.  This is safe and nontoxic.  Vitamin D level should be above 70 nmol/L.  Lifeguards and indigenous Pacific Islanders typically have levels between 80-100 nmol/L.   Levels lower than this are based on amount needed to prevent disease like rickets and osteomalacia. We need more thiamine when we're physically ill, emotionally and mentally stressed, and if we exercise like an athlete or laborer.  We need more thiamine if we eat a diet high in simple carbohydrates.  For every 500 kcal of carbohydrates, we need 500-1000 mg more of thiamine to process the carbs into energy.  If there's insufficient thiamine the carbs get stored as fat.  Again, recommended levels set for thiamine are based on minimum amounts needed to prevent disease.  This is often not adequate for optimum health, nor sufficient for people with absorption problems such as Celiac disease.  Gluten free processed foods are not enriched with vitamins like their gluten containing counterparts.  Adding a B Complex and additional thiamine improves health for Celiacs.  Thiamine is safe and nontoxic even in high doses.  Thiamine helps the mitochondria in cells to function.  Thiamine interacts with each of the other B vitamins.  They are all water soluble and easily excreted if not needed. Interesting Reading: Clinical trial: B vitamins improve health in patients with coeliac disease living on a gluten-free diet https://pubmed.ncbi.nlm.nih.gov/19154566/ Safety and effectiveness of vitamin D mega-dose: A systematic review https://pubmed.ncbi.nlm.nih.gov/34857184/ High dose dietary vitamin D allocates surplus calories to muscle and growth instead of fat via modulation of myostatin and leptin signaling https://pubmed.ncbi.nlm.nih.gov/38766160/ Safety of High-Dose Vitamin D Supplementation: Secondary Analysis of a Randomized Controlled Trial https://pubmed.ncbi.nlm.nih.gov/31746327/ Vitamins and Celiac Disease: Beyond Vitamin D https://pmc.ncbi.nlm.nih.gov/articles/PMC11857425/ Investigating the therapeutic potential of tryptophan and vitamin A in modulating immune responses in celiac disease: an experimental study https://pubmed.ncbi.nlm.nih.gov/40178602/ Investigating the Impact of Vitamin A and Amino Acids on Immune Responses in Celiac Disease Patients https://pmc.ncbi.nlm.nih.gov/articles/PMC10814138/
×
×
  • 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.