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

Where To Go From Here? I'm Baffled!


vegan lisa

Recommended Posts

vegan lisa Rookie

I'm totally baffled as to what to even discuss with my doctor. Here's a short summary of where I've been:

*Misdiagnosed with gastritis after suffering from stomach pain, which at the time I thought was heartburn. I know now that sharp pain under the left ribcage isn't heartburn, but that's what I thought it was back then. I was "treated" with nexium and diet (no spicy foods, no alcohol, no fried foods, etc). Got much, much worse. Regularly had D, black, tarry, loose stools, more pain. Joint pain continued, hormone issues continued (early menopause symptoms).

*After 6 months of suffering, I was referred to a GI who did blood testing (3 tests plus total IgA), an endoscopy with 3 biopsies, a CT scan, and a colonoscopy. All were normal. Blood results were 0. The biopsies were totally clear. However, at this point I HAD developed actual heartburn!

*I quit taking nexium. Aside from the pain in my stomach and the D for 3 hours most mornings, joint pain and menopause stuff, the rest went away. No more oily stools, NO MORE Heartburn!! Bad Nexium!

*My GI doctor said "You do not have any of the illness which I treat." and dismissed me as a patient.

*At this point, I took matters into my own hands. I quit eating any foods I thought were suspicious: gluten, apples, and honey. I felt 90% better. NO joint pain, no heartburn, but still had occasional mild stomach pain, an occasional D that I couldn't be sure was from cross contamination or some other food I had eaten. I had a few slip-ups that I was aware of, but it's so hard to draw that direct connection between the oatmeal I ate and the 4 days of D, brain fog and fatigue. Maybe I was just fighting some virus?

*So my regular doctor referred me to a GI specialist at a big research hospital at a University a few hours from where I live. He looked at my biopsy slides again, and said there was mild inflammation in my stomach and in the join of the esophagus and stomach. (Duh, the nexium I was taking gave me heartburn!) For what it's worth, he did seem very knowledgeable about celiac and non-celiac gluten sensitivity/intollerance. He really thinks celiac is unlikely. He decides that my pain might be from the stomach acid and puts me on Zantac and gives me the go ahead to eat whatever I want. This was last week.

I've been taking Zantac for 4 days, and I reintroduced apples (still no honey or gluten). I feel awful. I have heartburn every single minute. I have that horrible taste in my mouth, and my whole chest hurts. I've had a constant mild headache (known side effect). My stools are getting dark and oily again. The doctor's idea was that the histamine blocker in Zantac would help me reintroduce foods, but so far, not good with apples.

So what do I do now?? Do I try wheat?? It seems so hard to draw any direct connections between symptoms and what I eat. There are too many variables! How long do I give the zantac? I've given up on apples to see if I feel better, and I don't yet. But, the apple thing seems really weird, right? I don't have problems with other high-fructose foods. Nor do I have much burping (except when I'm on a heartburn med!).

The new GI doc also wants to re-do the EGD, but what else could he be looking for? The meds that make people "forget" don't work for me. I remember every thing from my first EGD. I really don't want to put myself through that in a hospital 2 hours from home to get more inconclusive results, you know?

Any ideas/advice is welcome. I really don't know what to do, or if it's possible to make any progress with or without a doctor. There aren't any tests left to run! My food diary doesn't seem to be telling me much, either.

Thanks for reading my long saga!

Lisa


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



Celiac.com Sponsor (A8-M):



Takala Enthusiast

Q.

"..... but what else could he be looking for ?"

A. Insurance reimbursements.

This has been a simple answer to a simple question.

Q.

"...but what do I do now ?"

A. Stop eating foods that bother you, and stop taking medications which are making it worse. By eliminating the root cause, you may be able to reintroduce other safe foods back in.

ravenwoodglass Mentor

I would also say to stop the meds that are making you worse. You say you felt 90% better gluten free so do stay gluten free. Many of us react to oats so do drop those also. 4 days of D. brain fog and fatigue are typical 'I got glutened reactions'. Do you eat soy? That can also be a problem so eliminating that would be my next step.

If you have been gluten free the tests for celiac will be negative. If you want them to diagnose you for celiac you need to go back on gluten for 3 months or so.

cassP Contributor

the only antacid pill i'll take ever again is Zantac- and ONLY temporarily IF i have an ulcer...

its better to take something more mild like Pepto Bismol or tums (gluten-free ones only).. because the proton pump inhibitors can make things worse- they shut down your stomach so that it cant make stomach acid.. but if your stomach is not in the middle of an ulcer- it NEEDS all your stomach acid.. if your stomach doesnt have enough stomach acid- then that sphincter between the stomach and esophagus will loosen and not clamp down.. and then whatever acid is left in your stomach will leak into your esophagus.

plus- if you reduce your stomach acid too much- you then cant digest foods properly.. and it creates an environment in which H.Pylori LOVE to flourish in.

apples CAN be problematic not just because of the fructose, but because of it's acidity. if i were you, i would avoid apples untill you've got this whole thing figured out.

good luck, hope you find your answers

canutillo Rookie

My dd19 is cannot eat apples. Or any fruit with a pit. I would stop with the apples. Then when you are feeling good again, it is up to you if you want to try gluten. I wouldn't bother if you feel so much better.

It takes time to heal. I read somewhere that it can take up to 4 years for gluten to get out of your system. I have been gluten-free for a year and will still on occassion break out in a new patch of dh or feel really icky for a couple of days- but am still improving. So that feeling 90% better can still reach 100% with time.

Of course, there could be something else in your diet that effects you (corn, soy, dairy, etc)

vegan lisa Rookie

Thanks for your thoughts. I quit taking the Zantac, which as you all pointed out, makes perfect common sense! It took about 2 weeks to recover from the rebound reflux when I quit taking Nexium, but I'd been on that for 7 months. I've only been on Zantac for 3 days, so I hope to recover more quickly.

I put a call in to my GI, but am going to hold off on any food introductions until I feel better. The doctor insisted it would be fine to do all of this at once, but clearly it isn't fine.

I love apples, but it's not like they are hard to avoid, so that's an easy one to take out of my diet again. Thanks for the tip on apples, Ii didn't realize that it was a problem food for acid, espeicially since the foods I usually think of as acidic (tomatoes, citrus) are fine for me. I think.

Ok, off to think about something else before I start second guessing myself. Again.

Thanks for your replies. The first reply made me laugh! All of the replies were very helpful! I appreciate your time and wisdom!

Lisa

cassP Contributor

i know- i didnt always know that apples (esp. apple juice) can be too acidic...

im fine with tomatoes in moderation. lemons & grapefruit actually turn the stomach and body alkaline. and OJ-> i avoid like the plague!!!!!!! unless i wanna end up worshipping the porcelain god :(


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
      131,699
    • Most Online (within 30 mins)
      7,748

    RelievedP
    Newest Member
    RelievedP
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)

    • There are no registered users currently online

  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • cristiana
      @Gigi2025  Thank you for your interesting post.  Some of what you say chimes with something my gastroenterologist tells me - that he has clients who travel to France and find the same as you  - they will eat normal wheat baguette there without issue, for example.  His theory was he thought it might be to do with the locally sourced wheat being different to our own in the UK? But I have to say my own experience has been quite different. I have been to France twice since my diagnosis, and have been quite ill due to what was then (pre-2019)  poor labelling and cross-contamination issues.  My TTG test following my last visit was elevated - 'proof of the pudding', as we say in the UK!  It was not just a case of eating something like, say, shellfish, that disagreed with me - gluten was clearly an issue. I've also been to Italy to visit family a couple of times since my diagnosis.  I did not want to take any chances so kept to my gluten free diet, but whilst there what I did notice is that coeliacs are very well catered for in Italy, and many brands with the same ingredients in the UK are clearly marked on the front of their packaging that they are 'senza glutine'.  In the UK, you would have to find that information in the small print - or it puts people off buying it, so I am told!  So it seems to me the Italians are very coeliac aware - in fact, all children are, I believe, screened for coeliac disease at the age of 6.  That must mean, I guess, that many Italian coeliacs are actively avoiding gluten because, presumably, if they don't, they will fall ill?        
    • deanna1ynne
      Thank you both very much. I’m pretty familiar with the various tests, and my older two girls with official dxs have even participated in research on other tests as well. I just felt overwhelmed and shocked that these recent results (which I found pretty dang conclusive after having scott clean labs just six months ago) would still be considered inconclusive. Doc said we could biopsy in another six weeks because my daughter was actually way more upset than I anticipated about the idea of eating it for years before doing another biopsy. It doesn’t hurt her, but she’s afraid of how it may be hurting her in ways she can’t feel. She’s currently eating mini wheats for breakfast, a sandwich with lunch, and a side of pasta along with every dinner, so I’m hoping we’re meeting that 10g benchmark mentioned in that second article!
    • knitty kitty
      Have you tried a genetic test to look for Celiac genes?  No gluten challenge required.  
    • knitty kitty
      Hello, @ElisaAllergiesgluten, Have you tried going on a low histamine Paleo diet like the Autoimmune Protocol diet?  A low histamine AIP diet would help your body rid itself of the extra histamine it's making in response to allergies.  Are you Celiac as well?   Since we need more thiamine when we're stressed, adding Benfotiamine, a form of Thiamine Vitamin B 1, can help the body calm down it's release of histamine.  Benfotiamine improves Sailors' asthma.  
    • knitty kitty
      Don't skimp on the gluten daily while undergoing the gluten challenge!  
×
×
  • 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.