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

Advice On Bringing Up Concerns With Gluten To Doctors


Sunshine Sassie

Recommended Posts

Sunshine Sassie Rookie

Hi everyone,

 

I had my first GI appointment today (for colonoscopy) but the GI seemed to think my case wasn't severe enough to do a colonoscopy; or any other tests. I am pleased to hear that information (was not looking forward to a colonoscopy) but disappointed that he would not run any other test (x-ray, etc.) I feel like I am in too much pain for it to just be IBS. He prescribed me an anti-depressant to help cope with the pain and told me to take Miralax once a day for a month and then come back.

 

I have been experimenting with gluten since May and know that it contributes to my pain if not is the cause. I didn't bring it up to him because I felt like he had his mind made up that I have IBS and was scared to say anything.

 

Does anyone have any advice on bringing up gluten to your doctor? I feel like the doctors don't understand how severe my symptoms are and do not take me seriously. I may have a complex about it because I am only 25.

 

I am eating gluten every day to be tested; if I ever get the courage to bring it up to my doctor. I have had a blood test when I was not eating gluten and it came back negative and IGA deficient.


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



Celiac.com Sponsor (A8-M):



Georgia-guy Enthusiast

Sunshine,

First of all, welcome! (As I do not think I have seen any of your prior posts)

Like you, I have had issues with my doctors believing things I say. It's been a long journey that has ultimately lead to me having to get an pay for blood work at a private lab. I do not wish that upon you, and I do t really recommend it.

As far as what you can do to get your doctor to listen and at least consider gluten as the problem, start keeping a "food and symptom journal". Write down exactly what you eat, when you eat it, any symptoms that start, when they start, how long they last, and every doctor's favorite question "how bad on a scale of 1-10?" Doing this will give you some ammunition to bring to your doctor showing gluten may be the problem. You may also want to do things like have pasta tonight, then in a few days make the exact same dish with a gluten free pasta and toppings to see if there are the same symptoms. when recording symptoms, I would recommend using the side of caution. If anything feels out of how a 100% healthy person would feel, write it down as a symptom. Do NOT be afraid of your doctor, your doctor works for YOU, not the medical facility. If your doctor ignores your complaints, you may want to find a new one. Try doing some research to see if there are any doctors in your area that specialize in celiac disease. You can also look for a local celiac support group and if there is one, ask them want doctors their members use (and definitely see if you are welcome to come to meetings!).

Keep in mind as well that being IgA deficient (I'm guessing you got that from a "total IgA test" showing a deficiency) is rather common with celiacs. Since that is the case, I would ask that the doctor run the IgG based tests next time. By any chance do you happen to have a copy of the actual results from the last test and the lab "normal" ranges?

(As a side note, I no longer feel like the baby on here as I am 25 as well.)

nvsmom Community Regular

Yes, GeorgiaGuy has s right. With low IgA, you'll need the IgG based tests which are tTG IgG, DGP IgG, EMA IgG (if available), and ay be the old AGA IgG. The IgA based tests will almost always be falsely negative in a celiac with low IgA, which occurs in 5% of celacs.

You'll need to keep eating the gluten for about 8-12 weeks for the tests to be accurate.

Good luck with the doctor. I understand about doctor nerves, I actually did a home test and brought it in to my doctor for proof (it was an IgA based test so it would not work for you).

Best wishes.

Jmg Mentor

Does anyone have any advice on bringing up gluten to your doctor? I feel like the doctors don't understand how severe my symptoms are and do not take me seriously. I may have a complex about it because I am only 25.

 

I am eating gluten every day to be tested; if I ever get the courage to bring it up to my doctor. I have had a blood test when I was not eating gluten and it came back negative and IGA deficient.

 

This is what I wish someone had told me at round about your age, maybe a little earlier.

 

Doctors earn their status but they're not infallible and no GP can know everything about every condition, it's impossible. They are all under time / cost pressures and however well meaning will naturally want to progress your case and move on to the next as quickly as possible. 

 

No-one will ever know as much about your body as you do and no-one will ever have a bigger stake in getting the right answers. Be confident and assertive, if your body is telling you something then trust it and make sure you communicate it clearly to your Doctor. By all means take the prescribed medicine and advice but don't allow yourself to be fobbed off with something that will treat a symptom without also if possible making some progress towards determining its cause.  

 

If your eating gluten now it would make sense to make an appointment for a test so, if it does turn out to be a problem for you,  your not doing that for longer than strictly necessary. So make that your goal for your next appointment, write down some bullet points if that seems helpful. Get the test scheduled and take confidence from asserting yourself and taking ownership over your health.

 

That's pretty much what I'm doing now, I just really wish I'd done it years ago as the various symptoms I've experienced have had a big impact on me. 

Best of luck, hope you get the answers you need :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,741
    • Most Online (within 30 mins)
      7,748

    Kaz 1
    Newest Member
    Kaz 1
    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

    • Theresa2407
      Maybe you have a low  intolerance to Wheat.   Rye, Barley and Malt are the gluten in Celiac disease.  It has always been stated Wheat and Gluten, not just a Wheat intolerance.  Barley will keep me in bed for (2) weeks.  Gut, Migrains, Brain fog, Diahrea.  It is miserable.  And when I was a toddler the doctor would give me a malt medicine because I always had Anemia and did not grow.  Boy was he off.  But at that time the US didn't know anyone about Celiac.  This was the 1940s and 50s.  I had my first episode at 9 months and did not get a diagnosis until I was 50.  My immune system was so shot before being diagnoised, so now I live with the consequences of it. I was so upset when Manufacturers didn't want to label their products so they added barley to the product.  It was mostly the cereal industry.  3 of my favorite cereals were excluded because of this. Malt gives me a bad Gut reaction.
    • Gigi2025
      Thanks much Scott.  Well said, and heeded.   I don't have Celiac, which is fortunate.
    • Scott Adams
      Do you have the results of your endoscopy? Did you do a celiac disease blood panel before that?  Here is more info about how to do a gluten challenge for a celiac disease blood panel, or for an endoscopy: and this recent study recommends 4-6 slices of wheat bread per day:    
    • Scott Adams
      It is odd that your Tissue Transglutaminase (TTG) IgA level has bounced from the "inconclusive" range (7.9, 9.8) down to a negative level (5.3), only to climb back up near the positive threshold. This inconsistency, coupled with your ongoing symptoms of malabsorption and specific nutrient deficiencies, is a strong clinical indicator that warrants a more thorough investigation than a simple "satisfactory" sign-off. A negative blood test does not definitively rule out celiac disease, especially with such variable numbers and a classic symptomatic picture. You are absolutely right to seek a second opinion and push for a referral to a gastroenterologist. A biopsy remains the gold standard for a reason, and advocating for one is the most direct path to getting the answers you need to finally address the root cause of your suffering. Here is more info about how to do a gluten challenge for a celiac disease blood panel, or for an endoscopy: and this recent study recommends 4-6 slices of wheat bread per day:    
    • Scott Adams
      There is a distinction between gluten itself and the other chemicals and processing methods involved in modern food production. Your experience in Italy and Greece, contrasted with your reactions in the U.S., provides powerful anecdotal evidence that the problem, for some people, may not be the wheat, but the additives like potassium bromate and the industrial processing it undergoes here. The point about bromines displacing iodine and disrupting thyroid function is a significant one, explaining a potential biological mechanism for why such additives could cause systemic health issues that mimic gluten sensitivity. It's both alarming and insightful to consider that the very "watchdog" agencies meant to protect us are allowing practices banned in many other developed countries. Seeking out European flour and your caution about the high-carb, potentially diabeticgenic nature of many gluten-free products are excellent practical takeaways from your research, but I just want to mention--if you have celiac disease you need to avoid all wheat, including all wheat and gluten in Europe.
×
×
  • 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.