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

Thinking I Need To Be Gluten Free


lesliev523

Recommended Posts

lesliev523 Rookie

Hello-

I have had stomach issues for a few years now. I am a 38 year old female, and for the past four years or so, I have had trouble with constipation (to the point where my doctor felt I was becoming dependant on laxitives). I have been extremely bloated, with indigestion and acid reflux. Three years ago, I had appendicitis. Then about four months ago, I started to get gall bladder issues. At least we think. My HIDA scan was normal, but I showed polyps on my ultrasound. I did have an endoscopy, which resulted in some biopsies. As far as I know, the biopsies were normal.... although at the time I was focused on the gall bladder, so I am wondering if I should ask more questions on those results. I had my gall bladder out on Friday 9/16/11. I still feel like crap, although it could be a result of the surgery.

I am thinking of trying to go gluten free because while I was watching what I ate for my gall bladder, I noticed other things. Going low fat didn't necessarily make a difference. I did notice that ice cream, pizza, and burgers made me feel ill. But when I had a plain old order of french fries, I was fine. Beer also triggered me, but not in a stomach issue way... if I had a few beers, I noticed I was extremely stuffed up and congested the next day.

Does this sound like it could be gluten allergies? I am going for a follow up tomorrow, and am going to request a blood test for celiac.... as well as to be tested for other food allergies. I would love some feed back.

Thanks!


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



Celiac.com Sponsor (A8-M):



Marilyn R Community Regular

It definitely sounds like you're headed down the right road. Can you ask your GI for a copy of the radiology report from the endoscopy biopsies? I've had doctor's offices fail to report abnormal labs...

lesliev523 Rookie

It definitely sounds like you're headed down the right road. Can you ask your GI for a copy of the radiology report from the endoscopy biopsies? I've had doctor's offices fail to report abnormal labs...

That is a good idea. I asked my doctor about it today, and she said there was nothing indicating celiac. I am so frustrated.

So do I try to go gluten free until they decide to do the allergy tests? I have to wait a few more weeks before I can have that done because they want to make sure I am fully recovered from having my gall bladder out first. UGGH!! HELP!!

Roda Rising Star

I wouldn't think having your gallbladder out would affect the celiac blood tests.

lesliev523 Rookie

I wouldn't think having your gallbladder out would affect the celiac blood tests.

I agree.... but they think that I should start feeling better and that the issues I am having currently are related to the surgery. Honestly, I don't think it is. It is almost like I feel worse than I did before surgery. Sure, I am still surgery sore. But the nausea, cramping, and gas are so much worse than before. And I really don't think that those symptoms are surgery related.

I almost think that my doctors think I am silly for questioning gluten, and that they keep putting me off.

So should I just go gluten free and to hell with the testing?

Bubba's Mom Enthusiast

If you're still eating gluten I'd ask for a Celiac blood panel to be done at the very least. In some people (about 30%)the blood tests come back normal even with Celiac disease..and..you could still have a sensitivity/intollerance if not full blown Celiac.

Your symptoms sound like you have a problem with gluten.

If your Dr doesn't want to run the test, or if it comes back negative you can still try eliminating gluten on your own and see how you feel.

GB problems/symptoms are pretty common in Celiacs. Most Dr.s have a very narrow range of symptoms they think of in regards to the disease and are relunctant to test or DX it. Keep pushing for answers.

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. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      how much gluten do I need to eat before blood tests?

    2. - trents replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      IBS-D vs Celiac

    3. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      how much gluten do I need to eat before blood tests?

    4. - SilkieFairy posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      IBS-D vs Celiac

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

    • Total Members
      133,321
    • Most Online (within 30 mins)
      7,748

    James Minton
    Newest Member
    James Minton
    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

    • catnapt
      oh that's interesting... it's hard to say for sure but it has *seemed* like oats might be causing me some vague issues in the past few months. It's odd that I never really connect specific symptoms to foods, it's more of an all over feeling of unwellness after  eating them.  If it happens a few times after eating the same foods- I cut back or avoid them. for this reason I avoid dairy and eggs.  So far this has worked well for me.  oh, I have some of Bob's Red Mill Mighty Tasty Hot cereal and I love it! it's hard to find but I will be looking for more.  for the next few weeks I'm going to be concentrating on whole fresh fruits and veggies and beans and nuts and seeds. I'll have to find out if grains are truly necessary in our diet. I buy brown rice pasta but only eat that maybe once a month at most. Never liked quinoa. And all the other exotic sounding grains seem to be time consuming to prepare. Something to look at later. I love beans and to me they provide the heft and calories that make me feel full for a lot longer than a big bowl of broccoli or other veggies. I can't even tolerate the plant milks right now.  I have reached out to the endo for guidance regarding calcium intake - she wants me to consume 1000mgs from food daily and I'm not able to get to more than 600mgs right now.  not supposed to use a supplement until after my next round of testing for hyperparathyroidism.   thanks again- you seem to know quite a bit about celiac.  
    • trents
      Welcome to the celiac.com community, @SilkieFairy! You could also have NCGS (Non Celiac Gluten Sensitivity) as opposed to celiac disease. They share many of the same symptoms, especially the GI ones. There is no test for NCGS. Celiac disease must first be ruled out.
    • trents
      Under the circumstances, your decision to have the testing done on day 14 sounds very reasonable. But I think by now you know for certain that you either have celiac disease or NCGS and either way you absolutely need to eliminate gluten from your diet. I don't think you have to have an official diagnosis of celiac disease to leverage gluten free service in hospitals or institutional care and I'm guessing your physician would be willing to grant you a diagnosis of gluten sensitivity (NCGS) even if your celiac testing comes up negative. Also, you need to be aware that oats (even gluten free oats) is a common cross reactor in the celiac community. Oat protein (avenin) is similar to gluten. You might want to look at some other gluten free hot  breakfast cereal alternatives.
    • SilkieFairy
      After the birth of my daughter nearly 6 years ago, my stools changed. They became thin if they happened to be solid (which was rare) but most of the time it was Bristol #6 (very loose and 6-8x a day). I was on various medications and put it down to that. A few years later I went on this strict "fruit and meat" diet where I just ate meat, fruit, and squash vegetables. I noticed my stools were suddenly formed, if a bit narrow. I knew then that the diarrhea was probably food related not medication related. I tried following the fodmap diet but honestly it was just too complicated, I just lived with pooping 8x a day and wondering how I'd ever get and keep a job once my children were in school.  This past December I got my yearly bloodwork and my triglycerides were high. I looked into Dr. William Davis (wheat belly author) and he recommended going off wheat and other grains. This is the first time in my life I was reading labels to make sure there was no wheat. Within 2 weeks, not only were my stools formed and firm but I was only pooping twice a day, beautiful formed Bristol #4.  Dr. Davis allows some legumes, so I went ahead and added red lentils and beans. Nervous that the diarrhea would come back if I had IBS-D. Not only did it not come back, it just made my stools even bigger and beautiful. Still formed just with a lot more width and bulk. I've also been eating a lot of plant food like tofu, mushrooms, bell peppers, hummus etc which I thought was the cause of my diarrhea before and still, my stools are formed. In January I ran a genetics test because I knew you had to have the genes for celiac. The report came back with  DQ 2.2 plus other markers that I guess are necessary in order for it to be possible to have celiac. Apparently DQ 2.2 is the "rarer" kind but based on my report it's genetically possible for me to have celiac.  I know the next step is to bring gluten back so I can get testing but I am just not wanting to do that. After suffering with diarrhea for years I can't bring myself to do it right now. So that is where I am!   
    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
×
×
  • 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.