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

Pediatrician Won't Test For Celiac


scarlet-willow

Recommended Posts

scarlet-willow Rookie

I am a newly diagnosed Celiac. My gastro advised that we get my 3 boys tested, regardless of symptoms. Well... their ped will not test them unless they present with symptoms! I find this incredibly frustrating because I love our pediatrician. He has been my boys' only Dr and he's been very, very good. But everything I have read says that all 1st degree (and sometimes even 2nd degree) relatives should be checked for this.

I have a well-child appointment scheduled for October, so I can try to convince him again then. Maybe I can get him to reconsider. My other options would be going to a pediatric gastro (which will be a huge hassle with 3 very young children) OR paying otu of pocket for one of those any labs places to do it... which would probably be even more expensive.

Any thoughts or suggestions of what I can say to help convince out ped to test my boys now? I don't want to lie to him and say they have symptoms when they don't.


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



Celiac.com Sponsor (A8-M):



squirmingitch Veteran

What about calling your gastro & telling him the ped refuses to test your boys as he (the gastro) advised. Ask the gastro if he will test the boys. it's only a blood test --- no biggie for a blood draw --- it's not like only peds can draw blood from kids.

Darn210 Enthusiast

The GI is right in that your boys should be screened.

I'd call your GI's office and let him know that the ped won't test. Your GI can request the test for your boys or his office can call your pediatrician and let him know that the request has come through your GI.

When my daughter was diagnosed, her pedGI requested the testing for my son and recommended that my husband and I have our PCP request our screening test . . . he told us to let him know if we ran into any trouble but we didn't.

Darn210 Enthusiast

I apparently type at the pace of a snail as squirmingitch's post wasn't there when I started posting . . . and my post is FIVE minutes later. My old typing teacher would not be happy ;)

come dance with me Enthusiast

You can just see a GP for a blood test can't you?

eatmeat4good Enthusiast

I agree with telling your gastro that the ped won't test.

Then ask for a referral to a ped that will. Let your ped know that you will be going to another ped until you find one that will test your children since this is an inherited disease. You can tell him you are happy with his work except for this situation which is serious to you and your children.

Or see if your gastro will do it.

Or your GP.

Took me two years to find one that would agree to test my son. The excuse was that he didn't have classic symptoms and wasn't emaciated. Wrong.

He tested positive.

Roda Rising Star

My boys ped wouldn't test my boys either. They both were seeing a pediatric allergist/immunologist at the time and I got him to send me the order for the blood test. There was no problem at all. Both tested negative on blood work after I was diagnosed. I had oldest retested yearly and he was always negative. He has been gluten free for now a year and is doing wonderful. Two years after my diagnosis I had the youngest son retested and he was positive.


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



Celiac.com Sponsor (A8-M):



Mizzo Enthusiast

AS A LAST RESORT (and we had to do this ) I lied to my Dr about tummy pains to get myself and husband tested because he wouldn't budge. We waited a few weeks after my DD was confirmed and the household had been gluten-free to mention it again to the DR. saying we noticed changes when gluten-free in house to nonGf outside of house.

We preferred to keep this doc and have had NO other problems with him but this.

StephanieL Enthusiast

Your GI wont be able to order the tests for your kids. Only a Dr. seeing the patient can order testing. You can have your Dr. send a letter to your Ped about the fact that it's genetic and they the kids need to be tested. If your Ped still won't I would seek out a new Ped or get a referral from your Ped for a pediatric GI who would most likely do the testing.

Good luck! The medical community has so much to learn about Celiac :(

squirmingitch Veteran

Your GI wont be able to order the tests for your kids. Only a Dr. seeing the patient can order testing. You can have your Dr. send a letter to your Ped about the fact that it's genetic and they the kids need to be tested. If your Ped still won't I would seek out a new Ped or get a referral from your Ped for a pediatric GI who would most likely do the testing.

Good luck! The medical community has so much to learn about Celiac :(

But I would make sure your GI tells the ped exactly which tests to order. Since the ped has refused to test them then it stands to reason that he won't know what the full celiac panel consists of.

MitziG Enthusiast

What an arrogant jerk. So tired of doctors who forget why they have a job. Definitely get a letter from the GI with the specific tests and demand he run them. If not, take your business elsewhere.

1974girl Enthusiast

I agree with getting the GI to send over the order. They do it all the time. And request like someone else said that he asks for the WHOLE panel. (EMA included) Some labs won't do EMA unless Ttg is positive so not sure how that really works.

I asked my ped. to test her since she has Hashimotos and dad is type 1 diabetic. She did it with no problem. She told me that it would be negative since she didn't have any symptoms but if she wanted me to, she'd do it. (I mean, WE are paying for it) She called me and said "I can't believe this but she is positive....waaaayyyyyy positive." I would get it done to prevent any other auto-immune diseases. The GI is hoping that by going gluten free, we can prevent my dd from getting type 1 diabetes like her dad did at 19. There are studies in lab rats that show it does help but then there is another one with humans that says it doesn't. Who knows but we are hoping for the best! (And taking vitamin D to help that along!)

mamaupupup Contributor

Gosh do I understand!!! It took me 18 months to get my kids tested...went through three doctors...

Our girls' GI will (and did) write orders for any of their first and second degree relatives.

You are not alone! Thinking of you! Keep up all your hard work!

come dance with me Enthusiast

I'm not familiar with the medical system over there, but here, a GP can order a test without any hassles.

frieze Community Regular

I am a newly diagnosed Celiac. My gastro advised that we get my 3 boys tested, regardless of symptoms. Well... their ped will not test them unless they present with symptoms! I find this incredibly frustrating because I love our pediatrician. He has been my boys' only Dr and he's been very, very good. But everything I have read says that all 1st degree (and sometimes even 2nd degree) relatives should be checked for this.

I have a well-child appointment scheduled for October, so I can try to convince him again then. Maybe I can get him to reconsider. My other options would be going to a pediatric gastro (which will be a huge hassle with 3 very young children) OR paying otu of pocket for one of those any labs places to do it... which would probably be even more expensive.

Any thoughts or suggestions of what I can say to help convince out ped to test my boys now? I don't want to lie to him and say they have symptoms when they don't.

maybe he needs to understand that by not testing he is commiting malpractice?

mamaupupup Contributor

I agree with frieze...in fact my husband and I are both outraged at how poorly doctors behave...I used the word "criminal" to describe this case.

mushroom Proficient

I would more likely term it ignorance and/or willful negligence. :)

mamaupupup Contributor

agreed, mushroom! :) I was feeling very angry :angry:

  • 1 month later...
Skysmom03 Newbie

We did the exact same thing. My ped was fine with it because she said some people have it and dont even realize it. She said that 1st degree relatives need to get tested because of the risk of lymphoma , melanoma, and other cancers. My son had no symptoms either .... Sue enough his blood test was positive and according to biopsy results the GI believes he has had it for three years or so. I would find a different pediatrician. If you have insurance and they will pay for it, there is no reason why they couldn't do it.

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

      What are Celiac Disease Symptoms?

    2. - klmgarland replied to klmgarland's topic in Dermatitis Herpetiformis
      2

      Help I’m cross contaminating myself,

    3. - Scott Adams replied to klmgarland's topic in Dermatitis Herpetiformis
      2

      Help I’m cross contaminating myself,

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

      My only proof

    5. - Scott Adams replied to Colleen H's topic in Related Issues & Disorders
      1

      Methylprednisone treatment for inflammation?


  • 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):



  • Upcoming Events

  • Posts

    • 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.
    • Scott Adams
      Based on what you've described, it is absolutely possible you are dealing with non-celiac gluten sensitivity (NCGS).  Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If your symptoms go away on a gluten-free diet it would likely signal NCGS.   Your situation is a classic presentation: a negative celiac panel but a clear, recurring pattern of symptoms triggered by gluten. The symptoms you listed—particularly the extreme fatigue, bloating, neurological-psychiatric symptoms like depression and anxiety, and even the skin manifestations like facial flushing—are all well-documented in research on NCGS. It's important to know that you are not alone in experiencing this specific combination of physical and emotional reactions. The only way to know for sure is to commit to a strict, 100% gluten-free diet under the guidance of a doctor or dietitian for a period of several weeks to see if your symptoms significantly improve. It is also crucial to rule out other potential causes, so discussing these symptoms with a gastroenterologist is a very important next step.
×
×
  • 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.