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
      131,905
    • Most Online (within 30 mins)
      7,748

    Croissantl0v3r
    Newest Member
    Croissantl0v3r
    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

    • Scott Adams
      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:    
    • Xravith
      Yes, you are right. Indeed, I’ve been feeling anemic since the beginning of this week, and today I felt horrible during a lecture at the university, I was trembling a lot and felt all my body incredibly heavy, so I had to come back home. I’ll do a blood test tomorrow, but I’m just worried about the possibility of it coming back negative. I’ve been eating two cookies in the morning as my only source of gluten over the past two weeks—could that affect the final result?
    • trents
      Welcome to the forum, @Judy M! Yes, he definitely needs to continue eating gluten until the day of the endoscopy. Not sure why the GI doc advised otherwise but it was a bum steer.  Celiac disease has a genetic component but also an "epigenetic" component. Let me explain. There are two main genes that have been identified as providing the "potential" to develop "active" celiac disease. We know them as HLA-DQ 2.5 (aka, HLA-DQ 2) and HLA-DQ8. Without one or both of these genes it is highly unlikely that a person will develop celiac disease at some point in their life. About 40% of the general population carry one or both of these two genes but only about 1% of the population develops active celiac disease. Thus, possessing the genetic potential for celiac disease is far less than deterministic. Most who have the potential never develop the disease. In order for the potential to develop celiac disease to turn into active celiac disease, some triggering stress event or events must "turn on" the latent genes. This triggering stress event can be a viral infection, some other medical event, or even prolonged psychological/emotional trauma. This part of the equation is difficult to quantify but this is the epigenetic dimension of the disease. Epigenetics has to do with the influence that environmental factors and things not coded into the DNA itself have to do in "turning on" susceptible genes. And this is why celiac disease can develop at any stage of life. Celiac disease is an autoimmune condition (not a food allergy) that causes inflammation in the lining of the small bowel. The ingestion of gluten causes the body to attack the cells of this lining which, over time, damages and destroys them, impairing the body's ability to absorb nutrients since this is the part of the intestinal track responsible for nutrient absorption and also causing numerous other food sensitivities such as dairy/lactose intolerance. There is another gluten-related disorder known as NCGS (Non Celiac Gluten Sensitivity or just, "gluten sensitivity") that is not autoimmune in nature and which does not damage the small bowel lining. However, NCGS shares many of the same symptoms with celiac disease such as gas, bloating, and diarrhea. It is also much more common than celiac disease. There is no test for NCGS so, because they share common symptoms, celiac disease must first be ruled out through formal testing for celiac disease. This is where your husband is right now. It should also be said that some experts believe NCGS can transition into celiac disease. I hope this helps.
    • Judy M
      My husband has had lactose intolerance for his entire life (he's 68 yo).  So, he's used to gastro issues. But for the past year he's been experiencing bouts of diarrhea that last for hours.  He finally went to his gastroenterologist ... several blood tests ruled out other maladies, but his celiac results are suspect.  He is scheduled for an endoscopy and colonoscopy in 2 weeks.  He was told to eat "gluten free" until the tests!!!  I, and he know nothing about this "diet" much less how to navigate his in daily life!! The more I read, the more my head is spinning.  So I guess I have 2 questions.  First, I read on this website that prior to testing, eat gluten so as not to compromise the testing!  Is that true? His primary care doctor told him to eat gluten free prior to testing!  I'm so confused.  Second, I read that celiac disease is genetic or caused by other ways such as surgery.  No family history but Gall bladder removal 7 years ago, maybe?  But how in God's name does something like this crop up and now is so awful he can't go a day without worrying.  He still works in Manhattan and considers himself lucky if he gets there without incident!  Advice from those who know would be appreciated!!!!!!!!!!!!
    • Scott Adams
      You've done an excellent job of meticulously tracking the rash's unpredictable behavior, from its symmetrical spread and stubborn scabbing to the potential triggers you've identified, like the asthma medication and dietary changes. It's particularly telling that the rash seems to flare with wheat consumption, even though your initial blood test was negative—as you've noted, being off wheat before a test can sometimes lead to a false negative, and your description of the other symptoms—joint pain, brain fog, stomach issues—is very compelling. The symmetry of the rash is a crucial detail that often points toward an internal cause, such as an autoimmune response or a systemic reaction, rather than just an external irritant like a plant or mites. I hope your doctor tomorrow takes the time to listen carefully to all of this evidence you've gathered and works with you to find some real answers and effective relief. Don't be discouraged if the rash fluctuates; your detailed history is the most valuable tool you have for getting an accurate diagnosis.
×
×
  • 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.