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

Finally Seeing A Gi -- Any Advice?


gatita

Recommended Posts

gatita Enthusiast

I've been gluten-free for six months now and my joint and GI symptoms are much better, though the the GI ones still flare up. I was never endo'd, only had three blood tests (anti-gliadin IgA,TTG and total IgA) that were normal; and then a followup one for anti-gliadin IgA that was a high positive.

My doc couldn't do the endo because my duodenal ulcer was too inflamed (and he wondered if maybe the 'ulcer' is actually villi damage). So he had me try going gluten-free, and after a few months of that showed intolerance, it was too late to do more blood tests. I know, I know... it's all bass ackwards!

So I'm pretty sure my official diagnosis says 'gluten intolerant' without a definitive rule-out of celiac.

I can no longer tolerate wheat or gluten at all, so a gluten challenge would be hard.

Soooo.... It's taken me months to finally get a GI appointment, now what should I ask him to do?

I'd like to get nutrition testing (I know people have often posted here which tests to get but darn, I'm having a hard time finding them via search).

Are there any other tests/services I should ask him for?

I'm also worried he's an "IBS guy" and will just try to put me on IBS drugs, but there doesn't seem to be any celiac expert in our small county.

Thanks for listening y'all... :)


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

You will need to test levels of vitamins A, B's (especially B12 and folate), D, E and K, and iron/ferritin, potassium, magnesium, calcium, zinc. Also get your thyroid checked (TSH, free T3, free T4 and TPO antibodies).

gatita Enthusiast

You will need to test levels of vitamins A, B's (especially B12 and folate), D, E and K, and iron/ferritin, potassium, magnesium, calcium, zinc. Also get your thyroid checked (TSH, free T3, free T4 and TPO antibodies).

Thank you! I wouldn't even have thought of thyroid...

mushroom Proficient

Thank you! I wouldn't even have thought of thyroid...

Thyroid problems are probably the most common co-rider autoimmune problem for celiacs. :)

And by the way, don't accept any "IBS" prescriptions. Just tell him you prefer to get to the bottom of problems rather than mask them.

Takala Enthusiast

Take the test results from the other doctor, too, so he doesn't try starting some Wild Goose Chase.

Celiac Mindwarp Community Regular

Maybe write down your questions. I always forget by the time I get in the office. My new GI took my paper and wrote to me with answers to all my questions. Wow.

gatita Enthusiast

Thanks for the good ideas!

I did print out my test results and will show him. Also wrote up a one-page health history starting with the lactose intolerance I was born with, LOL. (Couldn't even drink mother's milk).

I will also print a list of questions (including the list of tests you've given me).

Mushroom, I do plan to push back on the IBS thing and am not at all interested in their IBS drugs. It's bad enough I have to take the occasional Immodium when work etc. calls for it.

Mindwarp, that's amazing your GI wrote to you with answers. Wow is right.


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



Celiac.com Sponsor (A8-M):



gatita Enthusiast

Just a quick followup. The doc was GREAT! He never mentioned IBS at all, yay!!!!!!! He read my one-page medical life story and my questions and really appreciated that I'd done that.

He suspects celiac despite my previous negative blood test. He believes I also have SIBO caused by my gluten intolerance. I'm doing antibiotics for that followed by minimum three months on probiotics. He ordered the HLA gene test, endoscopy, colonoscopy, malabsorption stool tests, and vitamin deficiency and h pylori tests. Whew....

I noticed that under allergies, my chart now says "wheat" which I'm glad of because now I have something official to show even if the other tests come up negative. He sounded like he will at the very least diagnose NCGI after the tests are over.

What was interesting was he said our local biopsy folks are incredibly well trained to spot celiac, and he thought that even though I've been gluten-free for six months they might still find some damage. That surprised me.

He left it up to me as to whether I want to do a 2-week gluten challenge before the endo, but said he doesn't usually recommend it for someone with symptoms as bad as mine. (He seems to be up on the latest research where some specialists are now saying two weeks is often long enough for a gluten challenge.)

Anyway, thanks again for the suggestions, it all went better than I'd hoped!

mushroom Proficient

Oh, I am so glad you found a "keeper". Not many of us are that lucky! You go, girl !!

Celiac Mindwarp Community Regular

That is great, so glad you got a wow too!!

I ended up with an NCGI diagnosis after genetic testing, which he took seriously, and sent me to adietician..

Hope all the testing and diagnosis go well, sounds like you really found a good one :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,804
    • Most Online (within 30 mins)
      7,748

    Sister Sip Sip
    Newest Member
    Sister Sip Sip
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      This article, and the comments below it, may be helpful:    
    • nanny marley
      Oh yes I can understand the tiredness after going threw all that, must be exhausting especially on the mind I have high aniexty so I can understand that , I wish there more easier ways for people to get help , I had a MRI on my spine some years ago without anything it was really quick and no prep , I understand the need for  them to see better with the bowel ,but you think they would use something a little less traumatic  for ibd sufferers on the bowels by now ,I hope your feeling better today 🙏
    • Colleen H
      I wonder if tingling burning feet are part of it.. I'm not sure if it's the med reaction that people with gluten intolerance get or the food we ate  It's frustrating because a person who did not want to admit to himself I had this condition wanted me to eat this chicken sandwich and now I'm stuck with a variety of symptoms plus now I'm hungry on top of it..  I'm new to this so I forget that "one bite" of the wrong thing can hurt us.😔. Do we stop eating if someone exposed us to gluten ??  My stomach is rumbling but my joints hurt ...  It's weird because I can feel the anxiety coming on.  I get joint problems ,  I don't know if anyone ever got hot flashes?? I suppose if it affects people head to toes you can get that too.   It's weird...hard to decipher what is what.   Also how long do I have to deal with this attack??  Makes me feel like not getting up out of bed.  I get too many symptoms which  horrible.  Thank you for your response..  
    • wellthatsfun
      as my last post stated, i was diagnosed via endoscopy on the 14th of june. i have been eating amazing home cooked meals, luckily, mainly cooked by my boyfriend who is extremely careful about contamination (and is an incredible cook at that). however, i find myself in a mental rut still. being 18, this is the time in my life where i should be exploring things, going out, having fun. yet every corner i turn i'm tortured by the amazing smell of something i can't have anymore. the wonderful sight of such yummy foods. it's near torture. if my boyfriend and his friend who lives with us buy something i can't have, they'll usually eat it outside of the house or the car or wherever we are - which is greatly appreciated - but even seeing a burger or chips or a sausage roll in their hands guts me almost beyond repair. i just wanna have it again too. i miss it. i feel left out and it makes me very sad all the time. it's not their fault. they are allowed to eat whatever they want to, whatever their intestines will allow. it just stings, bad. and i feel so ungrateful given i basically have a private chef who is doubly the love of my life. but it's just so hard. i know i'll adapt. i haven't given up hope.i just wanted to vent. thank you for reading
    • RDLiberty
      Thank you. I must have misinterpreted a study or something. Thank you for the clarification. Much appreciated. Almost three years into my celiac diagnosis and I'm still learning new things. 
×
×
  • 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.