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

My Blood Work Was Very Expensive - I'm Very Upset


Carolita

Recommended Posts

Carolita Rookie

Hello all.

I got the bill for my blood work on Friday and they are charging me $899.00 :blink:

My insurance will not cover it b/c where I work they offer a very weird insurance where they give you a certain amount of $ (no much) and then is up to you to pay until you meet a deductible. Anyway, it will be out-of-pocket. I didn't know the blood work would be that much. I'm very upset about it.

Also, the doctor wants to see me to tell me I have Celiac disease. I called the nurse and asked if they could tell me over the phone what I need to know. The nurse talked to the Dr. and she basically told her she needed to see me b/c Celiac is a very rare disease and that I will not understand over the phone what I need to know. That made me very upset. They want to charge $57 for the visit and explanation. Do you think is worth going to the appointment. I don't want to be sick or jeperdize my health but I'm not paying $57.00 so she can tell me to stay away from Gluten. I don't know. Maybe there is more to it. What do you guys think?

Please help.

Thanks!!!!!!

Carol :(


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



Celiac.com Sponsor (A8-M):



wolfie Enthusiast

OUCH!!! Sorry that you have to pay that out of pocket. :( Is the dr aware that you are paying that amount out of pocket and that you really can't afford another $60 for them to tell you to eat gluten-free? There could be other health issues related to Celiac that he/she wants to discuss with you, though.

Good luck!

mommida Enthusiast

The doctor may want to run more tests for vitamin and nutrient defiency related problems/diseases associated with Celiac.

I would personally spend the 57 bucks on some gluten free food staples you will need and ask for a copy of the tests.

(Did I read somewhere there is a Celiac support network that actually sends out a gluten free food basket for newly diagnosed? Or is that just certain doctors or hospitals?)

L.

Carolita Rookie

Hello Kim.

I'm not sure. I talked to the nurse and I hope she conveyed the information. I get the impression that the nurse doesn't want to get involved :(

Thanks ... I might go see her. I have another appointment on the 20th to get my second Hepatitis B shot for school.

Carol :unsure:

_____________________________________________

Hello Mommida.

Thanks for the reply. I don't know about the free basket. What do you mean by gluten free food staples? I'm still very new at this.

Thanks for your help,

Carol :(

wolfie Enthusiast

Maybe you could combine those 2 into 1 appointment? That may save you some $$.

I know it stinks....we have a high deductible, too. Most of our well care is covered at 100%, but a lot of testing/urgent care stuff isn't.

penguin Community Regular

Ouch! Sorry your insurance wouldn't cover it! My insurance covered all but $2 of it (I have really good insurance), but what you're being charged is about what my insurance got charged.

Personally, I don't think the appointment would be worth it at this point. Your first flag is that his nurse said "celiac is a rare disease", which tells me they probably have outdated information. Even my doctor told me I'd find out more doing research on my own than what she or a nutritionist could tell me. I would say that you research it yourself and then make an appointment for a follow-up 3-6 months down the line to see how you are progressing.

Just my take.

Carolita Rookie

Kim ... I think I'll go get my lab results and ask if we can convine both appointments. I can read what the results say and try to make some sense of it. I have tried doing that in the past. I think though, they wanted to see me soon ... I hope is nothing really bad :(

So, in general insurances don't cover Celiac testing / urgent care? I thought it was just mine b/c is not a very good one.

Carol :unsure:

________________________________________________

Thanks Chelsea. I will be leaving my job very soon and going back to school so I will have a different insurance (offered by the school) around June so I hope it will cover it. Hopefully they don't come back with some excuse about it being a pre-existing condition. I hate being sick. Not only does one have to deal withe the disease but with the insurance as well.

Thanks for your input. I knew I could count on your guys.

Carol ;)


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor
Hello all.

I got the bill for my blood work on Friday and they are charging me $899.00 :blink:

My insurance will not cover it b/c where I work they offer a very weird insurance where they give you a certain amount of $ (no much) and then is up to you to pay until you meet a deductible. Anyway, it will be out-of-pocket. I didn't know the blood work would be that much. I'm very upset about it.

Also, the doctor wants to see me to tell me I have Celiac disease. I called the nurse and asked if they could tell me over the phone what I need to know. The nurse talked to the Dr. and she basically told her she needed to see me b/c Celiac is a very rare disease and that I will not understand over the phone what I need to know. That made me very upset. They want to charge $57 for the visit and explanation. Do you think is worth going to the appointment. I don't want to be sick or jeperdize my health but I'm not paying $57.00 so she can tell me to stay away from Gluten. I don't know. Maybe there is more to it. What do you guys think?

Please help.

Thanks!!!!!!

Carol :(

Carol, Make sure your doctor knows your financial situation, not all but some will reduce your bill. Also if you are in state that has any kind of medical assistance program you may be able to get help with that bill under a emergency program. If the lab was located in your local hospital you can also go to their finacial offices and ask for help with problem. Most hospitals have programs to cover stuff for people who are under or not insured. They don't always let that fact be readily known so don't assume there is no help available without asking first.

Carolita Rookie

Thank you Ravenwoodglass. I'll do that. I think it was done at the hospital since the bill came from them. I called the hospital and they told me they forwarded it to my insurance and are waiting on them to reply so I'll wait and see what happens. Maybe I woun't have to pay all of it.

Thanks,

Carol ;)

ravenwoodglass Mentor
Thank you Ravenwoodglass. I'll do that. I think it was done at the hospital since the bill came from them. I called the hospital and they told me they forwarded it to my insurance and are waiting on them to reply so I'll wait and see what happens. Maybe I woun't have to pay all of it.

Thanks,

Carol ;)

Also sometimes the insurance companies and the hospitals settle with themselves for a fraction of the cost. I well remember the first time I had 13 tubes of blood drawn and the bill was over $1000, but they actually got much less in the end. And welcome to the family, this board was a life saver for me there are soooo many nice, knowledgeable and even kooky folks around here.

tiredofdoctors Enthusiast

I'm with you on this one. My neuro doc drew an ataxia panel -- we got a letter FedEx'd to us by Athena Labs that stated they didn't know what the insurance was going to cover, but if we wanted to lock in a 20% co-pay, we could pay $1,299 by Visa, Mastercard, Discover or check by phone. If the insurance covered more than the 80%, they would refund the difference. Sure, let's go ahead and do that check by phone! I called today to cancel the testing. I don't know if I need to know that badly what type of genetic garbage caused gluten to screw up my brain.

Carolita Rookie
I'm with you on this one. My neuro doc drew an ataxia panel -- we got a letter FedEx'd to us by Athena Labs that stated they didn't know what the insurance was going to cover, but if we wanted to lock in a 20% co-pay, we could pay $1,299 by Visa, Mastercard, Discover or check by phone. If the insurance covered more than the 80%, they would refund the difference. Sure, let's go ahead and do that check by phone! I called today to cancel the testing. I don't know if I need to know that badly what type of genetic garbage caused gluten to screw up my brain.

Hello Lynne.

Wow!!! Is better to wait and see what the insurance will do. I understan what you mean. Medical treatment is getting more expensive by the minute :( Hope you fee better soon.

Thanks,

Carol ;)

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - marlene333 replied to Grace Good's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Bee balm lipbalm not gluten free

    2. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      4

      Related issues

    3. - Scott Adams replied to catsrlife's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      Patiently Waiting to See Results

    4. - catsrlife replied to catsrlife's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      Patiently Waiting to See Results

    5. - Jmartes71 replied to Jmartes71's topic in Coping with Celiac Disease
      4

      Related issues


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,261
    • Most Online (within 30 mins)
      7,748

    Pbaentine
    Newest Member
    Pbaentine
    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

    • marlene333
      To play it safe, use Vasoline Lip Therapy. No questions as to it containing gluten.
    • Mari
      jmartes, Thank you for sharing  more information with us. Most of us Celiacs whose problems do not clear up with in a few years have to decide what to do next. We can keep seeing DR.s and hope that we will get some  medication or advice that will improve our health. Or we can go looking for other ways to improve our health. Usually Celiac Disease is not a killer disease, it is a disabling disease as  you have found out. You have time to find some ways to help you recover. Stay on your gluten-free diet and be more careful in avoiding cross contamination . KnittyKitty  and others here can give you advice about avoiding some foods that can give you the gluten auto immune reaction and advice about vitamins and supplement that help celiacs. You may need to take higher doses of Vit. B12  and D3.  About 20 years before a Dr. suggested I might have Celiac disease I had health problems that all other Dr said they could not identify or treat. I was very opposed to alternative providers and treatments. So many people were getting help from a local healer I decided to try that out. It was a little helpful but then, because I had a good education in medical laboraties she gave me a book  to read and what did I think. With great skeptism I started reading and before I was half way through it I began using the methods outlined in the book. Using those herbs and supplements I went from hardly able to work to being able to work almost fulltime. I still use that program. But because I had undiagnosed celiac disease by 10 years later some  of my problems returned and I started to loose weight.    So how does a person find a program that will benefit them? Among the programs you can find online there are many that are snake oil scams and some that will be beneficial. by asking around, as I did. Is there an ND in your area? Do they reccomend that person? If you would like to read about the program I use go to www.drclark.net   
    • Scott Adams
      It's unfortunate that they won't work with you on this, but in the end sometimes we have to take charge of our own health--which is exactly what happened to me. I did finally get the tests done, but only after years of going down various rabbit holes and suffering. Just quitting gluten may be the best path for you at this point.
    • catsrlife
      My doctor didn't take the time to listen to anything. I don't even think she knows what it means. She is more concerned about my blood pressure that is caused by her presence than anything else and just wants to push pills at me. The so-called dermatologist wouldn't do a skin test. she prescribed all of these silly antihistamine skin meds. This lady didn't even know what she was talking about and said "they never turn out as celiac, they usually just say it's dermatitis so here's your meds," just like my regular quack. I'm trying to change insurance companies at the moment and that has been a battle because of red tape, wrong turns, and workers having wrong phone numbers. What a joke! The allergy blood days say I have a wheat allergy of .31. Hopefully it's just that and until I find a decent doctor and dermatologist, I'll just lay off the wheat anyway, since it gives me asthma, high blood sugar, and joint pain. So frustrated at this point. The rash on my back of arms/elbows is mostly gone. Both calves and chest have started up. smh. It comes and goes. It fades faster now, though, although my forearms still produce one or two bumps on each side. The itching has calmed down a lot except for the bump area. I have dry skin to begin with so anything affecting it just makes it crazy. i'm never going to eat wheat again. I don't care if they need it to produce results or if it is just an intolerance, allergy, or celiac. It gives me hell.
    • Jmartes71
      I had the test done by one of the specialist through second pcp I had only a few months because he was saying I wasn't.Even though Im positive HLA-DQ2 .My celiac is down played.I am with new pcp, seeing another girl doctor who wants to do another breathe test next month though Im positive sibo this year.I have high blood pressure not sure if its pain from sciatica or sibo, ibs or hidden gluten. Im in disability limbo and I should have never been a bus driver because im still suffering and trying to heal with zero income except for my husband. This isnt fare that my health is dictating my living and having ti beg for being revalidation of my disregarded celiac disease. Its an emotional roller coaster I don't want to be on and the medical made it worse.New pcp new gi, exhausted, tired and really fed up. GI doctor NOT girl..
×
×
  • 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.