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

Results


124chicksinger

Recommended Posts

124chicksinger Apprentice

IGA Serum, high 560 - the doctor said nothing about it; didn't even mention it to me.

 

Tissue Transglutam AB IGA - 1  -  Antibody not detected

Tissue Transglutam Ab IGG - 1 - Antibody not detected

Endomysial SCR IGA w/rfl - negative

 

biopsy pathology - negative for celiac damage

 

------

While I'm happy with this, I do believe I'm gluten sensitive or intolerant. Also in reviewing this disease, candida comes up a lot with similar and same symptoms.  I was certain after the scopes the doctor said the inflammation in my esophagus could be related to yeast.  I mentioned this today, and he said "i would never say that."  Basically, he said that Metformin could be giving me some heartburn, and I should for the diverticulosis eat a high fiber diet with plenty of whole grains.  I'm as healthy as a horse, and I feel so ill. 

 

I told him I eliminated the obvious sources of gluten since the scoping and will continue on that path because perhaps I'm sensitive/intolerant.  His answer was "whatever...if you want to do that, do that."  I have the feeling he doesn't believe in gluten intolerance/sensitivity.  

 

I am done trying to put a name to whatever is causing my bloating and pain and apparently inflammation in my digestive tract.

 

Thank you everyone for listening to my issue while trying to find out and "diagnose" my ills.

 


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

Hi,

 

It's fine to go gluten-free without positive test results.  There are no tests for non-celiac gluten intolerance (NCGI) yet, so the  only way to know is to trial the gluten-free diet.  And there are probably a lot more people with NCGI than with celiac disease.  Do stick with the gluten-free diet for at least 6 months and record your results.  A food / symptoms diary can help you pinpoint food reactions.

nvsmom Community Regular

My kids were negative on their celiac disease tests too so now that they are gluten-free and feeling better, the improvement is viewed as a "coincidence" by their doctor. NCGI is very real and has basically all the same symptoms as celiac disease except the villi atrophy and the dh rash. Nasty! I hope you feel better soon on the gluten-free diet. :)

And ditto Paul, a food and symptom journal is really helpful to see patterns when most symptom changes are too slow to notice on a day by day basis.

cyclinglady Grand Master

I would give up gluten for six months. It is worth a try. My cousin gave up gluten after getting a negative endo. She feels much better. My husband gave it up 13 years ago without a formal dx.

Then you need to track your foods to see what might trigger other issues besides intestinal. Like red wine triggers my rosacea. I am allergic to milk proteins, nuts and intolerant to eggs and garlic. Besides being gluten-free, I am on a very low carb diet now to keep my blood glucose levels low. But after a year, I am finally feeling better.

I guess what I am saying is to not give up!

Oh, you have been diabetic for a long time. Did the GI check for gastroparesis which is caused by diabetic related nerve damage in the gut?

NoGlutenCooties Contributor

 I have the feeling he doesn't believe in gluten intolerance/sensitivity.  

 

You may want to find a new doctor.  Doctors tend to be very slow to accept anything that cannot be cured with a drug.  It is as if it goes against their DNA.

I agree with the others on this one... try going 100% gluten free for a few months and see how you feel.  If that isn't enough to convince you, go back to eating gluten and see if your symptoms come back.  If you have non-Celiac gluten intolerance then the results of this self-test will be enough to convince you never to touch the stuff ever again - no matter what the doctors say.

124chicksinger Apprentice

Thank you all for your responses.  Cycling lady, thank you for mentioning gastroparesis; I saw that during my "research" into my symptoms, and I do not think it is that (no nausea or vomiting), and I have been Dtype2 for about 14 years.

 

For 10 days now, since I had the scopes, I am eating gluten free, even looking for/avoiding the hidden gluten.  To my surprise, I am not hungry.  I have no cravings at all, not even for the obvious carbs.  I started taking a probiotic 2 days ago. I am logging all meals, glucose readings, bathroom habits, and weight.

 

Is it okay to continue to post here even tho the tests state I am not celiac? I don't want to be considered a poser.  I plan to be gluten-free for at least 3 months and see what difference it makes.

cyclinglady Grand Master

Of course you are welcome at this forum! It is for anyone struggling from the effects of eating gluten or those helping family or friends.


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



Celiac.com Sponsor (A8-M):



GottaSki Mentor

Absolutely you are welcome...regardless of diagnosis we all struggle with the same issues.

NoGlutenCooties Contributor

 To my surprise, I am not hungry.  I have no cravings at all, not even for the obvious carbs.  

 

I didn't have any added hunger or craving issues either.  I've only been gluten free for coming up on 6 months and just had my first gluten-free roll a couple of weeks ago.  That was the first I even wanted anything close to bread.  Consider yourself to be very lucky... some people seem to have horrible withdrawal.

Oh... and of course you're welcome here!  Anyone with gluten issues is welcome - diagnosis or not.  :)

GFinDC Veteran

Yes, yes, u r berry, berry welcome here! :)

 

Lots of people come to the forum to try and figure out if they have a gluten related issue, and their tests don't show it yet or maybe never.  Since there is no accepted testing for NCGI, it leaves it up to us to figure out if we have it or not.  Docs ain't much help at the moment.  Even celiac testing has flaws and is not 100% accurate, after all these years.  The positive results are more accurate than the negative results..

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    2. - tiffanygosci posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Aldi Pueblo Lindo Yellow Corn Tortillas

    3. - tiffanygosci replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    4. - trents replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    5. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,978
    • Most Online (within 30 mins)
      7,748

    Beverley Blanchard
    Newest Member
    Beverley Blanchard
    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

    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
    • tiffanygosci
      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
    • trents
      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
    • Mari
      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
×
×
  • 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.