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

Doctor Didn't "say" I Have It


ardere

Recommended Posts

ardere Newbie

First time poster needing some advice. I'm unsure of my diagnosis given by my doctor because we only did a gene test which came back positive. I have quite a history of evidence to consider. I know that most of you aren't doctors but it would be great if I got some opinions.

 

- Haven't been able to eat cakes since I was about 11(over 9 years ago), they always made me as bloated as a pregnant heifer.

- Over 2 years asgo I was diagnosed with lactose intolerance and was still able to eat bread and what not.

- Just under a year ago I started having problems with eating bread and I went gluten-free on my own accord. The doctor did a blood test then but since I hadn't been eating nothing came up and he said I was just gluten sensitive. 

- I avoided gluten but skipped every now and then and felt ill... Come last week I got my results from my DNA test from doc who said I was positive but we didn't do a biopsy cause I was not interested in feeling bad for 6 weeks and he agreed that was for the best.

- When I told my mum it was a genetic thing she said that her and my grandma don't eat bread because it makes them blotted!(they never got tested)

 

What I'm questioning is do I have celiac? Doctor never said I have celiac, just that my results are positive. At one point I thought it was all in my head before I spoke to me doctor. Do you need to have a positive gene and biopsy test to be diagnosed? Even ATM I have reflux and my stomach won't stop grumbling from a "gluten free pizza base" I ate less than week ago which was contaminated. 

 

Sorry for the rant, de Nile isn't just a river in Egypt!


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



Celiac.com Sponsor (A8-M):



1desperateladysaved Proficient

My doctor believed I had celiac when she saw my genetic results.  Mine showed 2 copies of HLA DQ2 and 2 copies of HLA DQ8.  I had been off gluten for 3 weeks.  I looked 5 months pregnant.  I shared my symptoms after going gluten free.  She told me I had celiac and should never eat gluten again.  Over time, since, I read the forum so much I discovered that you can have the genes without the disease.  This made me and other doctors question my diagnosis.  I did not think it would be ethical to eat the gluten for me to test, so I went on.  Since, I have found many things that back the diagnosis.

 

I have food intolerances beyond gluten.  I drank so much milk as a child, yet the dentist felt my bone mass was low.  The enamel had disappeared off my teeth when I was 17 years old.  I had foggy brain and fatigue that went away on the gluten free diet.  I had heel pain in one foot or the other for a few years.  When I went gluten free, both feet began to hurt at the same time.  Then the pain went away and never came back!

 

I spoke with a new MD the other day.  She didn't seem to be "buying my celiac"  I told her that I had been deficient in vitamin B, iron, Vitamin D, and magnesium (perhaps others) in spite of the fact I supplemented them.  When she heard that these levels had come up, she seemed to relax.  You might try to get as early of a baseline on nutrient levels as possible and compare later readings.  I think if you are eating a healthy diet, but have low nutrient levels it would indicate something is wrong with digestion.

 

If you weren't eating gluten when you did the blood test, it could be false negative.  One doesn't usually have antibodies to something they haven't eaten recently.  But are you avoiding all gluten or just major sources?

 

Hopefully, you will get a definitive enough for you diagnosis.  If you should be totally gluten free  you will do it.  I wish you the best in good health.

 

D

kareng Grand Master

A doctor isn't likely to diagnose you with Celiac based on a gene test.  About 30% of the population has the gene but only about 1% have Celiac.  If you want a "real" diagnosis, you would need to eat gluten for a few months and get re-tested.

 

At this point, you know gluten makes you feel bad.  Its up to you if that is enough of a reason to eat gluten-free.

 

Open Original Shared Link

 

Open Original Shared Link

ardere Newbie

He said it's probably not worthwhile doing a biopsy because of prior symptoms. Are biopsies the only conclusive way to know if you have celiac?

nvsmom Community Regular

Most doctors seem to like to diagnose with a biopsy or a biopsy with blood tests. Some doctors are willing to diagnose with positive blood tests alone,  Some doctors are aware that having the positive genes, a family history of celiac disease, and reactions to gluten makes it pretty likely you have celiac disease, but I'm not sure if the give a diagnosis with that or not - probably depends on the doctor.

 

Welcome to the board, BTW.  :)

Archived

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

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

    • Total Members
      132,629
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Jmartes71
      Shingles is dormant and related to chicken pox when one has had in the past.Shingles comes out when stress is heightened.I had my 3rd Shingles in 2023.
    • knitty kitty
      Here's one more that shows Lysine also helps alleviate pain! Exploring the Analgesic Potential of L-Lysine: Molecular Mechanisms, Preclinical Evidence, and Implications for Pharmaceutical Pain Therapy https://pmc.ncbi.nlm.nih.gov/articles/PMC12114920/
    • Flash1970
      Thank you for the links to the articles.  Interesting reading. I'll be telling my brother in law because he has a lot of pain
    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
×
×
  • 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.