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

Where in San Francisco area should I get an Endoscopy? (Anthem Blue Cross, for < $10,000!)


SFmaybeCeliac

Recommended Posts

SFmaybeCeliac Newbie

I'm trying to find a decent place to get an endoscopy for celiac -- I had a highly recommended doctor at Kaiser, but am now on Anthem Blue Cross, and an endoscopy is very expensive at UCSF where my GI doctor recommended it.  It can be 10,000$ without insurance, would still be $2000 with my great no-deductible EPO plan!

Other places seem to be much cheaper (as low as $1000, which would end up costing me $200). But I have no idea if they are reputable and competent at celiac diagnosis (all I have is the the occasional yelp review, usually for a colonoscopy...).

Do you have any recommendations? Or know someone who might, who I can private message? I can check to see if they are covered by my insurance. 

 

For reference, it's important that the doctors be pretty competent -- my previous endoscopy was negative, but my ttg tests are 4x normal and going up every time I'm tested -- so I want to have confidence that I won't get a false negative!


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



Celiac.com Sponsor (A8-M):



Scott Adams Grand Master

You might get some of the names of doctors who do the least expensive procedures and check them here:

Open Original Shared Link

SFmaybeCeliac Newbie

Thanks, that's helpful as a bare minimum :)

Though I I'm hoping to find someone who not only is not bad, but someone who is explicitly recommended for Celiac diagnoses, given that I've already had one potential false negative (from a highly regarded doctor). Perhaps there is some directory for this too?

Scott Adams Grand Master
cyclinglady Grand Master

Will your insurance run the rest of the celiac panel or was that already done?   The TTg is often used for initial screening.  A positive result usually requires a full celiac panel as the next diagnostic procedure before  biopsies.  

Open Original Shared Link

 

SFmaybeCeliac Newbie

Hmm. These are my results: 

  • Tissue Transglutaminase Antibody, IgA: 77.6 (standard:  <20.0 CU)
  • Gliadin Ab IgA, Deamidated: 15.5  (standard: <20.0 CU)
  • Gliadin Ab IgG, Deamidated: 57.5 (standard:  <20.0 CU)
  • IgM, serum:  80 (standard: 39 - 333 mg/dL)
  • IgG, serum: 867 (standard: 672 - 1760 mg/dL)
  • IgA, serum:  169 (standard: 89 - 581 mg/dL) 

Is that considered a full celiac assay and expected results? 

cyclinglady Grand Master

Just the EMA is missing.  That test, if I recall, is very specific to celiac disease but is expensive to run.  You have a positive on the DGP IGG though.  Two positives, I would say that you mostly likely have celiac disease but I am not a doctor!  

It is recommended that more that four biopsies are taken.  This will help insure that they catch damaged areas.  The small intestine is vast (stretched out the size of a tennis court).  It is 22 or so feet long. Even Dr. Joseph Murray, GI at Mayo Clinic and one of the leading celiac disease experts in the US, has said that it is easy to miss damaged areas (heard that on a video recently).  So celiac disease tests are not perfect.

Do you have a copy of your previous biopsy and endo reports?  

Do you mind if I ask what were your initial symptoms?  

Here is more reading:

Open Original Shared Link

 


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



Celiac.com Sponsor (A8-M):



  • 2 weeks later...
SFmaybeCeliac Newbie

Thanks so much for your detailed reply.  Unfortunately I missed the email about it or I would have responded sooner. 

I had 10-12 biopsies taken.

This is the report summary and symptoms:
FINAL PATHOLOGIC DIAGNOSIS SMALL INTESTINE, DUODENUM, BIOPSY: - NO SIGNIFICANT PATHOLOGIC ABNORMALITY. STOMACH, BIOPSY: - NO SIGNIFICANT PATHOLOGIC ABNORMALITY. NO H. PYLORI-LIKE ORGANISMS IDENTIFIED. 3/2014 DQ2+, DQ8 negative
Currently gets colds periodically, no other GI symptoms. Has 2-3 BM/day, no pain. Stool is formed to soft. Good appetite though not very high calorie diet. Usually 2-3 meals/day. 
 

Do you know if there is a way to find the EMA test / get my insurance to do it? According to my doctor "My system won't let me order the endomysial antibody for some reason"

I'm still looking for a place to do an endoscopy too, though I'm running out of time before the end of the year. :/

cyclinglady Grand Master

Aren't any of your doctors able to recommend a GI doctor?  I know you are trying to find a cheaper endoscopy, but if it were me, I would pay the $2k even if I had to get a second job or borrow from family and friends.  But only you can make that decision since you know your financial circumstances.  You had two positives on the celiac panel.  Getting the EMA test.  How is that going to help?  Will you go gluten-free if that is positive or what?  I do not understand.  Your insurance will cover an endoscopy, right?  

I do not mean to be harsh, but we are talking about your health.

SFmaybeCeliac Newbie

I appreciate your concern! 

The reason I am hesitant to get a second endoscopy is that I don't have any real reason to expect it to be positive. It was negative before, not much has changed, and it costs much more at UCSF than anywhere else almost, but I'm just not sure where else I should trust. 

So it seems dumb to spend so much money in it, if I can find a better option. (either another highly specific test, or an alternate less expensive trusted location)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,902
    • Most Online (within 30 mins)
      7,748

    Patty6133
    Newest Member
    Patty6133
    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

    • 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.
    • Scott Adams
      In this case the beer is excellent, but for those who are super sensitive it is likely better to go the full gluten-free beer route. Lakefront Brewery (another sponsor!) has good gluten-free beer made without any gluten ingredients.
    • trents
      Welcome to the forum, @catsrlife! Celiac disease can be diagnosed without committing to a full-blown "gluten challenge" if you get a skin biopsy done during an active outbreak of dermatitis herpetiformis, assuming that is what is causing the rash. There is no other known cause for dermatitis herpetiformis so it is definitive for celiac disease. You would need to find a dermatologist who is familiar with doing the biopsy correctly, however. The samples need to be taken next to the pustules, not on them . . . a mistake many dermatologists make when biopsying for dermatitis herpetiformis. 
×
×
  • 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.