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

Healthcare Ins. And Celiac


sebbitt01

Recommended Posts

sebbitt01 Newbie

Sooo, we have been seeing a GI specialist for 8 months. Originally my 1 year old daughter had chronic diarrhea she had undigested sugars in her stools and a very high level of bad bacteria in her gut. So they said probably Celiac. We had some blood work done, and she tested Neg for IgA Atigladin (lovel level of IgA in general) but had an elevated level of IgG (triple the normal). Also High Neutrophil count, Low Lymphocyte level and VERY low Alkaline phosphate levels. We are starting a Gluten Free Diet today because insurance will not approve the biopsy. She is 2 years and 2 month old and weighs 23 pounds. She does not heal well at all (5 week for a mosquito bite) ... Has anybody faced this issue with insurance or anything similar to the blood work? Any ideas on how to deal with our insurance?

Thanks!!


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



Celiac.com Sponsor (A8-M):



Dixiebell Contributor

Can you post the results of the tests? A lot of people here are quite good at understanding those. There is a newer test DGP, you could see if they would do that one too.

Roda Rising Star

If you really want to try and persue the biopsy you could have her doctor write a letter explaining why they feel the need for the exam and petition the insurance company to cover it. IMHO it would cost them a whole lot less in the long run to find out now than many years of doctor visits etc if you were to not choose to go gluten free. My insurance does not pay for any genetic testing, but I had my youngest son's allergist/immunologist and ped write a letter to the insurance company to pay for a test they didn't cover for him. They were testing him for LAD (leukocyte adhesion deficiency and luckily he didn't have it) and they were testing genetic markers. I have never recieved a bill from the lab to this day and that was almost 5 years ago. But in the off chance you don't have luck with the insurance company, it certainly won't hurt anything to try the diet.

Mizzo Enthusiast

Sooo, we have been seeing a GI specialist for 8 months. Originally my 1 year old daughter had chronic diarrhea she had undigested sugars in her stools and a very high level of bad bacteria in her gut. So they said probably Celiac. We had some blood work done, and she tested Neg for IgA Atigladin (lovel level of IgA in general) but had an elevated level of IgG (triple the normal). Also High Neutrophil count, Low Lymphocyte level and VERY low Alkaline phosphate levels. We are starting a Gluten Free Diet today because insurance will not approve the biopsy. She is 2 years and 2 month old and weighs 23 pounds. She does not heal well at all (5 week for a mosquito bite) ... Has anybody faced this issue with insurance or anything similar to the blood work? Any ideas on how to deal with our insurance?

Thanks!!

No help here, just my story.

We had np problem with the biopsy as our GI ordered it. However when it came to me and my husband getting the bloodwork on ourselves based on the GI recommendation our Primary care would not order the test due to lack of symptoms. So I suddenly ;-) had celiac like symptoms and insisted on the bloodwork (an aunt on my mom's side also has Celiac so it was an easy push). My husband who actually has stomach problems took longer to convince the PC but eventually we both got tested.

good luck.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,032
    • Most Online (within 30 mins)
      7,748

    CE1963
    Newest Member
    CE1963
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
    • Scott Adams
      Those are driving distance from me--I will try to check them out, thanks for sharing!
    • Scott Adams
      I am so sorry you're going through this bad experience--it's difficult when your own lived reality of cause and effect is dismissed by the very professionals meant to help you. You are absolutely right—your violent physical reactions are not "what you think," but undeniable data points, and it's a form of medical gaslighting to be told otherwise, especially when you have a positive HLA-DQ2 gene and a clear clinical picture. Since your current "celiac specialist" is not addressing the core issue or your related conditions like SIBO and chronic fatigue, it may be time for a strategic pivot. Instead of trying to "reprove" your celiac disease to unwilling ears, consider seeking out a new gastroenterologist or functional medicine doctor, and frame the conversation around managing the complications of a confirmed gluten-free diet for celiac disease. Go in and say, "I have celiac disease, am strictly gluten-free, but I am still suffering from these specific complications: SIBO, chronic fatigue, dermatological issues, and high blood pressure linked to pain. I need a partner to help me address these related conditions." This shifts the focus from a debate about your diagnosis to a collaborative plan for your current suffering, which is the help you truly need and deserve to work toward bouncing back.
    • NanCel
      Hello, no I had to have them re done and then used a liner over the top.  Many dentists are not aware of the celiac effects.  Best of luck.   There is other material, yet, very expensive.
    • sleuth
      He is not just a psychiatrist.  He is also a neuroscientist.  And yes, I have already read those studies.   I agree with benfotiamine.  This is short term while glutened/inflammation occurs.  As I had already mentioned, these symptoms no longer exist when this phase passes.  And yes, I know that celiac is a disease of malnutrition.  We are working with a naturopath.
×
×
  • 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.