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

Need Help With School Project


Debby

Recommended Posts

Debby Newbie

My daughter is doing a school project on Celiac and I was wondering if

a few people would help her out and just answer a question for her.

"I'm a student doing a report on Celiac and I am trying to emphasize

how common the disease is as well as encourage the public to become

more aware of it. For part of my project I am inquiring on how much

money in doctor bills people have spent before being diagnosed.

(including what insurance paid) Thank you for any help your can give

me" Kim


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



Celiac.com Sponsor (A8-M):



gfgypsyqueen Enthusiast

I can't give you an exact amount, but I have been in many emergency rooms as a child with abdominal pain. As a young adult I had years of health problems and lables of bulemia and IBS (neither were correct). Throw in a couple of surgeries "to look around". Then I finally started getting really sick. My undiagnosed illness affected my new baby too. She's ok in the end. I finally lost a gallbladder and an appendix and got a diagnosis of Celiacs. Now I am much healthier. In total I would guess around $7K to $10K for my costs on surgeries, medications, lab work, etc. How much it ran without insurance I don't know.

For my toddler, the meds, lab work, and testing has run around 3K and she still does not have an "official" diagnosis. She responded really well to the diet after an inconclusive biopsy for Celiacs.

Hope the school project turns out well. Post the results :)

Debby Newbie

Thank you so much for your help!

I will let you know how my report goes.

Debby Newbie

gfgypsyqueen

Is it possible to get a first name. I am required to have a name.

You can email it to

debbierb at hotmail

Thanks

Kim

I can't give you an exact amount, but I have been in many emergency rooms as a child with abdominal pain. As a young adult I had years of health problems and lables of bulemia and IBS (neither were correct). Throw in a couple of surgeries "to look around". Then I finally started getting really sick. My undiagnosed illness affected my new baby too. She's ok in the end. I finally lost a gallbladder and an appendix and got a diagnosis of Celiacs. Now I am much healthier. In total I would guess around $7K to $10K for my costs on surgeries, medications, lab work, etc. How much it ran without insurance I don't know.

For my toddler, the meds, lab work, and testing has run around 3K and she still does not have an "official" diagnosis. She responded really well to the diet after an inconclusive biopsy for Celiacs.

Hope the school project turns out well. Post the results :)

mtraezme Newbie

I would say I probably spent around $4,000 before I gave up on doctors and diagnosed myself because they refused to believe anything was wrong with me. My first name is Ezme. Good luck with the project. Tomorrow is our last day of school! :D

holiday16 Enthusiast

Never diagnosed officially with celiac, but over the past two years between me and insurance it adds up to about $13,000. I remember adding up a few years ago what it was up to and that came to about $20,000 so over $30,000 total when it's all said and done and that's probably conservative. My problems started in 1999 so that's about 9 years. Never had a biopsy so they can't say celiac, but do agree I have a problem with gluten.

Thankfully we have really good insurance, but I also spent alot of money out of pocket to see other Drs. that weren't covered by insurance. I know at least another $5000 on that and probably closer to $10,000.

debmidge Rising Star

Michael - spent about $7000 medical bills in a 30-year span; this does not include the free medical attention he received from the Veteran's Hospital (couldn't be much because they refused to give him medical testing - so if I had to put a price on it it ran about $600 in 1977 - some of these costs are before healthcare costs skyrocketed so they may seem low by today's standards, but iin 1977 I think an average annual salary was $12,000 and minimum wage was about $1.75 per hour.

As to insurance: it's hard to determine because for many years our insurance was free as my employer used to pay for it. So I'd have to say the insurance cost for the years it was not free was about : $20,000 (20 years of group rate health insurance premium) for one person ; and my employer during years of 1979 to 1988 when he paid it was about $2500 for one person (9 years of group rate health insurance premium)

Also, you have to add in the "loss of income" costs -- the loss of income for each day taken off of work to go for testing and the loss of income when you can no longer work due to your "un" or "mis" diagnosed disease. This is the true cost of illness: reduced income or no income and reduced or lost opportunity to work (i.e., turned down for promotion or raise because you "are out too much" or you are perceived as being "sickly." That's the monetary loss that society does not seem to want to add up and see it as the true cost (along with healthcare and health insurance) that is harming our society.

My husband's illness has cost us not only medical costs but 30 years of income that a healthy man would have made.


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

I can't give an exact number for all the time I was ill, 15 years to diagnosis after daily D set in but I was celiac since childhood, but the year before I was diagnosed we spent $17,000 (no that is not a typo) on my medical needs, the year after diagnosis we spent about $700. You would think insurance companies would be the ones to give the biggest push for testing since it resolves so many issues for so many people.

dollamasgetceliac? Explorer

In General I think it is in the 100, 000's for most patients... If you think of unnecessary surgeries that doctors do.

One of my Doctors said that many patients whom are diagnosed with abdominal problems, have the most unnecessary operations of all, because and I have heard this before that these patients keep running to the Doctor and then they get tiered of all the complaints and then they start operating.

The thing is the Doctors can't be blamed ( they usually only know what they have been taught) The hospitals are running a business, It is a business like any other.

Another doctor told me " Aha you suffer from headaches and stomach aches , that is the worse, the doctors hardly ever can really figure it out".

Idealy the Doctors would know more about Celiac, improve testing and get the word out, so that we can have happier healthier lives. :huh:

purple Community Regular

We spent $450 for the initial visit to an osteopath that diagnosed my daughter on the first visit as gluten intolerant. She never saw an md. Shes given up most gluten and if she does eat it she knows. So the diagnoses was right even though she has not had a biopsy. Praise God for direction!

Debby Newbie

I want to give a big THANK YOU to everyone that help me with my school project. So far I have finished my outline and have done my oral presentation and received 20/20.

Besides getting a good grade it's really great to educate all my fellow students and teachers that have never heard of celiac.

Thank you

Kim

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,650
    • Most Online (within 30 mins)
      7,748

    Alexandersgirl
    Newest Member
    Alexandersgirl
    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
      Did the GI doc give you any rational for stopping the Tylenol during the gluten challenge? I have never heard of this before and I can't imagine a good reason for it. Ibuprofen, maybe, because it is an anti inflammatory but acetaminophen?  I don't see that it would have any impact on the test results to take Tylenol.
    • Julie 911
      Good day! New members here and I have a question about medication. My gastroenterologist made me stop some medication during the gluten challenge beforenthe screening test but I have a little surgery tomorrow and I need to know if I can use tylenol for half a day or if it will give me false results using it.   Thanks 
    • Scott Adams
      I agree, there can be contamination at many points--milling is another possible source of contamination for any flours.
    • trents
      Keep in mind that with manufactured food products, "gluten free" doesn't equate to no gluten. Things that are naturally gluten free can be cross-contaminated with gluten in the field, in shipping and in processing. In the U.S. companies can use the gluten free label as long as the product doesn't exceed 20ppm of gluten. That amount still may cause a reaction in some people.
    • deanna1ynne
      Dd10 was tested for celiac four years ago bc two siblings were dx’d (positive labs and biopsies). Her results at the time were positive ema  and ttg (7x the UL), but a negative biopsy. We checked again three months later and her ttg was still positive (4x the UL), but ema and biopsy were negative. Doc said it was “potential celiac” and to keep eating gluten, but we were concerned about harming her growth and development while young and had her go gluten-free because we felt the labs and ema in particular were very suggestive of early celiac, despite the negative biopsies. She also had stomach aches and lethargy when eating it. We just felt it’d be better to be safe than sorry. Now, four years later, she doesn’t want to be gluten-free if she doesn’t “have to be,” so underwent a 12 week gluten challenge. She had labs done before starting and all looked great (celiac panel all negative, as expected.) Surprisingly, she experienced no noticeable symptoms when she began eating gluten again, which we felt was a positive sign. However, 12 weeks in, her labs are positive again (ttg 4x the UL and ema positive again as well). Doc says that since she feels fine and her previous two biopsies showed nothing, she can just keep eating gluten and we could maybe biopsy again in two years. I was looking up the ema test and the probability of having not just one but two false positives, and it seems ridiculously low.  Any advice? Would you biopsy again? She’s old enough at this point that I really feel I need her buy-in to keep her gluten-free, and she feels that if the doc says it’s fine, then that’s the final word — which makes me inclined to biopsy again and hope that it actually shows damage this time (not because I want her to have celiac like her sisters, but because I kind of think she already does have it, and seeing the damage now would save her more severe damage in the long run that would come from just continuing to eat gluten for a few more years before testing again.)  Our doc is great - we really like him. But we are very confused and want to protect her. One of her older sibs stopped growing and has lots of teeth problems and all that jazz from not catching the celiac disease sooner, and we don’t want to get to that point with the younger sis. fwiw- she doesn’t mind the biopsy at all. It’s at a children’s hospital and she thinks it’s kind of fun. So it’s not like that would stress her out or anything.
×
×
  • 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.