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

Gluten Intolerance - Symptoms and Should I get Tested?


nacoconut

Recommended Posts

nacoconut Newbie

I think I may have gluten sensitivity. Or Celiac disease? I don't really know.

So, where to go from here? My Dr. said that I don't need to be eating gluten for my results to come back positive (I have heard the opposite). I don't think they will anyway, I'd be the unlucky person with negative results, and can they even detect a sensitivity over intolerance anyway? Supposedly, Celiac isn't in the family.  Should I just stop eating it, and if I feel better, know I shouldn't eat gluten and proceed with life? Or should I find a really good allergy Dr. and go to them? I'm just worried nothing will come up, as that's the norm unless I've broken a bone, and I'm tired of feeling horrible on a daily basis.

How do I know if I can still eat foods that are processed in a facility with wheat? Are all Celiacs/people with sensitivity affected?

My symptoms
- lifelong headaches, migraines
- Daily bloating (got way worse returning after living abroad for several months)
- fatigue (though I do eat well)
- some brain fog/ irritability/ mood swings
- depression (even though I am a happy person, happy with life)
- eczema on arms 
- random nausea 

I do not have any nutrient deficiency. I don't run to the bathroom 20 times after eating bread. I've tried to clear up my issues for years now and no one can figure out what's wrong.

Ps. I'm not allowing things to be stuck up me... and I'm not okay with anesthesia.
Thanks for the help!
 

 

 


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



Celiac.com Sponsor (A8-M):



SLLRunner Enthusiast

If you truly want to find out if you are celiac, you have to have blood tests and/or an endoscope which, as you guessee it, means a needle in your arm and/or a camera down your throat, and you do have anesthesia with the endoscope.  It is my understanding that the endoscope is the gold standard of diagnosing celiac disease because it involves biopsies of your small intestine tissue.  If I am incorrect about this someone will enlighten both of us.  :)

Here is an answer to your question about eating gluten prior to testing:
Open Original Shared Link

Here is also an article:  Open Original Shared Link

It sounds like you have been consulting with your doctor, but it sounds like he does not specialize in digestive issues. I would ask for a referral to a gastroenterologist, who does specialize in digestive disease. 

cyclinglady Grand Master

Ugh!  Your doctor sounds like he is not celiac savvy!  You must be consuming gluten daily (about 8 to 12 week) prior to a celiac blood panel.  If you are gluten free, your body will stop producing antibodies!  SSL Runner is right!  

Open Original Shared Link

I happen to be the first in my family to have celiac disease which is an autoimmune disorder (not an allergy) than runs in families.  My family is riddled with AI disorders (lupus, RA, MS, thyroiditis, etc.)  You could be the first in your family too!  Anemia was my primary symptom.  I had no known gut issues to gluten.  I went in for a routine colonoscopy (yeah, I'm in the over 50 club) and was shocked with the GI suggested celiac disease and ordered an endoscopy too.   But, he was right!  I had moderate to severe intestinal damage!  Both procedures were easy.  The colonoscopy (which is usually not ordered for celiac disease) prep was the hardest.  How much jello and clear broth can a person eat!  

If all celiac testing is negative, you could try going gluten free to see if symptoms resolve.  But diet adherence can be difficult (but not impossible) without a formal diagnosis.  

Your best bet is plenty of research.  See if you can get another doctor too.  

nacoconut Newbie

I do have a GI but haven't seen her in a few years. She was leaning towards lactose intolerance at first and we did a bunch of testing and I was also treated for parasite. She suggested an endoscopy but I won't do anesthesia. Is there a way to do it without? 

My GP said eating gluten free didn't matter, so I will be returning to the GI. Unless it is better to go to an allergy specialist? 

Just worried nothing will show up, and now my family thinks I'm a hypochondriac, hah. 

squirmingitch Veteran

You MUST be eating gluten for blood testing. I don't care what your doc says. If you don't keep eating gluten until the blood is drawn then you can get a false negative. It's happened countless times!!!!! 

An allergy specialist will do you no good in dx'ing celiac disease. Better to go to the GI. It may be possible to do the endoscopy under heavy sedation but not anesthesia but I'm not sure. I have a friend who did a colonoscopy where she watched it on the monitor so she was awake enough to do that.  You will have to discuss that with the GI. If you can work something out with the GI so you will have the endoscopy then you will need to continue eating gluten until the endoscopy is completed.

cyclinglady Grand Master

You could have an allergy to wheat and that is totally unrelated to celiac disease.  But, why are you so worried about having an endoscopy?  I have been "knocked out" for several things (C-section, gallbladder, etc.) and I can relate to your concerns (actually, my hubby worries more about this) but each time, the end result was well worth it.  

Did you know that most celiacs have lactose intolerance?  It is because the enzymes used to digest lactose are released from the villi tips.  If those are damaged from celiac disease, you can not digest lactose.  The intolerance varies with the degree of damage.  In many cases, based on genetics, you become lactose intolerant due to age or race.  It's like a huge chunk of the world population.  If you fall into that category, you will never overcome lactose intolerance.  

Get to your GI.  Keep eating gluten until all testing is complete.  And you are not a hypochondriac!

squirmingitch Veteran

nacoconut,

Apparently there are many options for the endoscopy procedure & you can do it without general anesthesia. Many people have gone through it with just a throat numbing spray. I found a few links I thought you might like to read:

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



nacoconut Newbie

Cyclinglady, 

Because of anesthesia as a child, I have extreme needle phobia to the point of either passing out, running out of the room, or being sedated which usually doesn't work once I see the needle. I'm doing my best, but some doctors have refused to take blood because of it. I will do this if I must but I don't know how I will react or what my GI will do.

I think I'm lactose sensitive as I can't do heavy ice creams or bisque anymore without having a stomach ache for the next 2 days. It has only become an issue within the last 4 years so that makes sense, before that no real issues but I didn't grow up on milk and prefer easier digested foods like yogurt and cheese.

All of this is making a lot of sense now! My mom has recently cut lactose, maybe I should urge her to get tested with me.

nacoconut Newbie

Squirm, thanks! I'll see if my GI can do this. I think she mentioned it being painful but I would rather deal with physical pain rather than needle anxiety!

manasota Explorer

It would not be unreasonable to ask for a mild sedative to be taken prior to even leaving your house.  You could  swallow a small tablet with a tiny bit of water.   Perhaps this would lessen your anxiety prior to getting the IV meds.  Might be worth a try.  You could even try a dose the evening before also.  DON'T LOOK AT THE NEEDLE!

nacoconut Newbie

Okay. I apparently already was tested, while eating plenty of gluten, and it came back negative. She suggested the endoscopy and I haven't been back in 2 years. I'm making an appointment.

How would I find out if it was a wheat allergy instead?

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. - Rogol72 replied to klmgarland's topic in Dermatitis Herpetiformis
      3

      Help I’m cross contaminating myself,

    2. - ShariW commented on Scott Adams's article in Frequently Asked Questions About Celiac Disease
      4

      What are Celiac Disease Symptoms?

    3. - klmgarland replied to klmgarland's topic in Dermatitis Herpetiformis
      3

      Help I’m cross contaminating myself,

    4. - Scott Adams replied to klmgarland's topic in Dermatitis Herpetiformis
      3

      Help I’m cross contaminating myself,

    5. - Scott Adams replied to Jmartes71's topic in Coping with Celiac Disease
      1

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,908
    • Most Online (within 30 mins)
      7,748

    ebrown
    Newest Member
    ebrown
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • Rogol72
      @klmgarland, My dermatitis herpetiformis didn't clear up until I became meticulous about cross contamination. I cut out gluten-free oats and all gluten-free foods, dairy and gluten-free rice. Additionally, getting the right amount of protein for my body weight helped significantly in my body's healing process ... along with supplementing with enough of all the vitamins and minerals ... especially Zinc and Magnesium. I went from 70kg to 82kg in a year. Protein with each meal 3 times daily, especially eggs at breakfast made the difference. I'm not sure whether iodine was a problem for me, but I can tolerate iodine no problem now. I'm off Dapsone and feel great. Not a sign of an itch. So there is hope. I'm not advocating for the use of Dapsone, but it can bring a huge amount of relief despite it's effect on red blood cells. The itch is so distracting and debilitating. I tried many times to get off it, it wasn't until I implemented the changes above and was consistent that I got off it. Dermatitis Herpetiformis is horrible, I wouldn't wish it on anyone.  
    • klmgarland
      Thank you so very much Scott.  Just having someone understand my situation is so very helpful.  If I have one more family member ask me how my little itchy skin thing is going and can't you just take a pill and it will go away and just a little bit of gluten can't hurt you!!!! I think I will scream!!
    • Scott Adams
      It is difficult to do the detective work of tracking down hidden sources of cross-contamination. The scenarios you described—the kiss, the dish towel, the toaster, the grandbaby's fingers—are all classic ways those with dermatitis herpetiformis might get glutened, and it's a brutal learning curve that the medical world rarely prepares you for. It is difficult to have to deal with such hyper-vigilance. The fact that you have made your entire home environment, from makeup to cleaners, gluten-free is a big achievement, but it's clear the external world and shared spaces remain a minefield. Considering Dapsone is a logical and often necessary step for many with DH to break the cycle of itching and allow the skin to heal while you continue your detective work; it is a powerful tool to give you back your quality of life and sleep. You are not failing; you are fighting an incredibly steep battle. For a more specific direction, connecting with a dedicated celiac support group (online or locally) can be invaluable, as members exchange the most current, real-world tips for avoiding cross-contamination that you simply won't find in a pamphlet. You have already done the hardest part by getting a correct diagnosis. Now, the community can help you navigate the rest. If you have DH you will likely also want to avoid iodine, which is common in seafoods and dairy products, as it can exacerbate symptoms in some people. This article may also be helpful as it offers various ways to relieve the itch:  
    • Scott Adams
      It's very frustrating to be dismissed by medical professionals, especially when you are the one living with the reality of your condition every day. Having to be your own advocate and "fight" for a doctor who will listen is an exhausting burden that no one should have to carry. While that 1998 brochure is a crucial piece of your personal history, it's infuriating that the medical system often requires more contemporary, formal documentation to take a condition seriously. It's a common and deeply unfair situation for those who were diagnosed decades ago, before current record-keeping and testing were standard. You are not alone in this struggle.
    • Scott Adams
      Methylprednisolone is sometimes prescribed for significant inflammation of the stomach and intestines, particularly for conditions like Crohn's disease, certain types of severe colitis, or autoimmune-related gastrointestinal inflammation. As a corticosteroid, it works by powerfully and quickly suppressing the immune system's inflammatory response. For many people, it can be very effective at reducing inflammation and providing rapid relief from symptoms like pain, diarrhea, and bleeding, often serving as a short-term "rescue" treatment to bring a severe flare under control. However, experiences can vary, and its effectiveness depends heavily on the specific cause of the inflammation. It's also important to be aware that while it can work well, it comes with potential side effects, especially with longer-term use, so it's typically used for the shortest duration possible under close medical supervision. It's always best to discuss the potential benefits and risks specific to your situation with your gastroenterologist.
×
×
  • 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.