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

Waiting On Results?


DestinyLeah

Recommended Posts

DestinyLeah Apprentice

Hi, I am new to the boards and had a question I was hoping someone could help with.

I was hospitalized a month ago, and the team of four docs on my case could not stop my vomiting and diarrhea without completely keeping food out of my system. My mom eventually asked for a GI specialist after a week of this tug-of-war with my digestive system, and negative tests for Cushing's Syndrome, parasites, infections, and viruses, along with four blown veins from the large amounts of potassium chloride and water they had to push into me to keep me functioning. The GI doctor asked my mom about my childhood and concluded that I may have celiac.

Two days later, I had positive results from blood tests (two different doctors had ordered the same test at once, both returned positive from separate labs) and was scheduled for an endoscopy. The endoscopy went well, but revealed a stomach ulcer not caused by H Pylori, and that 3/4 of my small intestine was nearly too injured to function at all. Biopsies were taken, and I was put on a gluten free diet. Within a week, I had regained the lost 10 pounds, was holding a steady heart rate and hydration level, and had gone longer without nausea and tummy pain than I had ever remembered before. I was released with a "tentative diagnosis" and told to call for results in another week.

I have called. And called... and called. It has been a month, and still the lab has no definite answers, as noone there knows what they are looking for, and a specialist had been called in at last check.

My insurance denied the entire claim for $42,000 and the hospital is demanding payment, but have yet to supply their end of the deal with a "yes" or "no".

After a month, can they even get the information they need from the biopsy, or is it no longer viable, and I will need a new one? :(


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



Celiac.com Sponsor (A8-M):



2kids4me Contributor

Biopsies dont go bad - not to worry. The samples are taken and then frozen and thin tissue slices taken and placed on a slide and stained.

It's frustrating to say the least that a histopathologist (the person who would examine your slide) hasn't written a report yet of his findings!

I would ask questions and find out why it's taking so long! Why would they have people looking at it - who have no clue? Isn't the "specialist", the one who should have looked at it all along?

Hope you get an answer soon.

Based on your response to gluten free, and the blood results - I think that is conclusive, at least in my mind

Sandy

ravenwoodglass Mentor
Hi, I am new to the boards and had a question I was hoping someone could help with.

I was hospitalized a month ago, and the team of four docs on my case could not stop my vomiting and diarrhea without completely keeping food out of my system. My mom eventually asked for a GI specialist after a week of this tug-of-war with my digestive system, and negative tests for Cushing's Syndrome, parasites, infections, and viruses, along with four blown veins from the large amounts of potassium chloride and water they had to push into me to keep me functioning. The GI doctor asked my mom about my childhood and concluded that I may have celiac.

Two days later, I had positive results from blood tests (two different doctors had ordered the same test at once, both returned positive from separate labs) and was scheduled for an endoscopy. The endoscopy went well, but revealed a stomach ulcer not caused by H Pylori, and that 3/4 of my small intestine was nearly too injured to function at all. Biopsies were taken, and I was put on a gluten free diet. Within a week, I had regained the lost 10 pounds, was holding a steady heart rate and hydration level, and had gone longer without nausea and tummy pain than I had ever remembered before. I was released with a "tentative diagnosis" and told to call for results in another week.

I have called. And called... and called. It has been a month, and still the lab has no definite answers, as noone there knows what they are looking for, and a specialist had been called in at last check.

My insurance denied the entire claim for $42,000 and the hospital is demanding payment, but have yet to supply their end of the deal with a "yes" or "no".

After a month, can they even get the information they need from the biopsy, or is it no longer viable, and I will need a new one? :(

First off welcome to the celiac world, hopefully you will feel better soon.

I am addressing the insurance denial, have you called the insurance company directly to find out why they denied? Sometimes it can be as simple as the hospital sent the bills to the wrong place, it has happened to me. They would simply resubmit. If they are withholding payment because you don't have a 'diagnosis' yet talking to someone at the insurance company might help also. It seems like this was definately an unjust denial, you do have the right to find out why and fight it. I would also contact the hospital itself and ask what is going on, they may be able to help also.

Stay gluten free and you have come to a great place for info and support. I hope they get everything straighted out with the billing soon.

DestinyLeah Apprentice

I got my diagnosis today. Funny story, that. I called the GI to ask for results, and the lady at the desk responded that my results were negative for Celiac. So I grabbed a cookie, but before I took a bite, got the feeling I should call back. I asked her to look back through my charts, just to be sure. She yet again said I was negative for Celiac, then I heard my doctor yelling at her to give the phone over. She told me that I tested negative for antibodies on blood drawn after having no food for two weeks, and that it was to be expected. She then told me that due to my progress and the genetic markers, she had asked for a second opinion on my biopsy results and sure enough, I had Celiac. The nurse at the desk had seen one negative result and told me that I was free to eat whatever I wanted. My doctor said the cookie could have put my life in danger because of the amount of damage already done to my body.

I guess we know ourselves enough to question things that go against our own *gut* feelings.

The insurance talked to us, though the hospital wouldn't. The hospital is refiling with them because what was wrong on the claim was simply the patient number on a couple of meds where a chart was mixed. They have recieved my results and are going to cover full costs when the hospital finishes cleaning up the records.

Lisa Mentor

Welcome also

When I read that you were about to take a bite out of that cookie...I yelled "NO" out load!! I bet you could here me. :o

I am relieved that you didn't and also relieved for you that the insurance is being re-addressed.

I am glad that you are feeling better. Stick with us as we travel this road together.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,972
    • Most Online (within 30 mins)
      7,748

    Hawaiian Snow
    Newest Member
    Hawaiian Snow
    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

    • Mari
      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
    • cristiana
      Interesting, when I suffered for a few months with ectopics I noticed that carbohydrates would cause indigestion and bloating in my stomach, then that would lead to my heart skipping beats, and I could feel it in my throat, it was very unsettling.  My last serious bout of this was after eating a Muller Rice Pudding for breakfast.   I happened to be wearing a 48 hour halter at the time and cardiology picked it up, but they weren't worried about what they saw. There was some British doctor who'd made some videos on the Vagus nerve that I remember watching at the time which made sense of what I was experiencing, there did seem to be some sort of connection.
    • Scott Adams
      Here are summaries of research articles on celiac disease and migraines: https://www.celiac.com/celiac-disease/celiac-disease-amp-related-diseases-and-disorders/migraine-headaches-and-celiac-disease/
    • Yaya
      I asked my cardiologist about stopping vitamins.  He said his tests account for all detectable vitamins from sources other than food.  I only need to stop them for a couple of days.  He has me keep records of meds and vitamins I've ingested over the past 10 days and prior and he does his calculations.   
    • jessysgems
      Reply to treats I try and eat to bring up the glucose. Sometime I get up 3 times a night and eat something. I don't think food is the issue. A lot of the food they say should help doesn't.  Many mornings my level is 59 and I feel sick, sometimes for hours. It has been recommended I go to an Endocrinologist.  
×
×
  • 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.