LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » CD57 LabCorp vs Quest

 - UBBFriend: Email this page to someone!    
Author Topic: CD57 LabCorp vs Quest
MamaBear11
LymeNet Contributor
Member # 25116

Icon 1 posted      Profile for MamaBear11   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
My LLMD has ordered a CD57 test through LabCorp. Problem is, my health insurance only covers tests done at Quest.

I have read in certain places that Quest doesn't even perform the test, which may give me ammunition to try to convince my insurance co. to cover it through LabCorp.

Does anyone know if that is still accurate and LabCorp is the only lab who does the CD 57 tests, or is it now just a matter of LabCorp being the only lab that provides reliable results?

--------------------
Untreated Lyme for 25+ years.
Two kids, too much pain & fatigue, no hope of ever being able to treat.

Posts: 310 | From Northeast | Registered: Mar 2010  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
LabCorp's test is the best out there. I agree that I don't think Quest even does the same test. They are really lame when it comes to anything but mundane testing. (like CBC's... they can probably handle that!!)

Did you find out how much the CD57 costs thru LabCorp??

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
MamaBear11
LymeNet Contributor
Member # 25116

Icon 1 posted      Profile for MamaBear11   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for the reply. I haven't found out yet how much it costs through LabCorp, but it wouldn't matter anyway, since I have no money to pay for it. So one way or another, I will have to find a way to convince my health insurance company to cover it if I want to have the test done.

The good news is, I think, that this test does not seem to be the definitive word in diagnosing Lyme disease. At least according to older threads from Lymenet that I have read tonight. So if I can't find a way to pay for it, it shouldn't be the end of the world.

--------------------
Untreated Lyme for 25+ years.
Two kids, too much pain & fatigue, no hope of ever being able to treat.

Posts: 310 | From Northeast | Registered: Mar 2010  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by MamaBear11:


The good news is, I think, that this test does not seem to be the definitive word in diagnosing Lyme disease. At least according to older threads from Lymenet that I have read tonight. So if I can't find a way to pay for it, it shouldn't be the end of the world.

You are absolutely correct! No worries at all on this one!

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
sk8ter
LymeNet Contributor
Member # 8671

Icon 1 posted      Profile for sk8ter     Send New Private Message       Edit/Delete Post   Reply With Quote 
Labcorp has a patient assist program that is a discount program...Call them and ask how much that test is on their discount program.
Posts: 871 | From orange county, ca. | Registered: Jan 2006  |  IP: Logged | Report this post to a Moderator
MichaelTampa
Frequent Contributor (1K+ posts)
Member # 24868

Icon 1 posted      Profile for MichaelTampa     Send New Private Message       Edit/Delete Post   Reply With Quote 
It is about $150-$200 from LabCorp before any insurance payments. Absolutely correct that Quest does not have it. I do think there is one other lab that does it, I read that somewhere, but it was not Quest.
Posts: 1927 | From se usa | Registered: Mar 2010  |  IP: Logged | Report this post to a Moderator
BackinStOlaf
Frequent Contributor (1K+ posts)
Member # 23725

Icon 1 posted      Profile for BackinStOlaf     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am pretty sure that labcorp is the best for that test

--------------------
First Symptom 9/09
Multiple docs, negative Labcorp test
LLMD: 1/10
Positive Igenex/CDC test
Treatment 2/10
2/10-8/10 Amox, ceftin, zith, flagyl
Currently: Bicillin, Minocycline, still dealing with severe breathing issues

 -

Posts: 1121 | From New York, New York | Registered: Dec 2009  |  IP: Logged | Report this post to a Moderator
MistyB
Member
Member # 27969

Icon 1 posted      Profile for MistyB     Send New Private Message       Edit/Delete Post   Reply With Quote 
It's weird - my insurance only covers Labcorp, but not Quest... and since we were new to the policy, I had a bunch of stuff done at Quest (waiting for that fun bill to come in).

I have also heard that Quest doesn't do CD57 - and my doc does them at Labcorp.

misty

--------------------
12yo Daughter w/severe anxiety, fatigue, dizziness, BPII - IGM 41+, 23+ and IGG 66+, 41+
Self - Undiagnosed - have peripheral neuropathy, hearing loss, facial tics, fatigue and a MRI w/lots of lesions.

Posts: 26 | From Worcester, MA | Registered: Sep 2010  |  IP: Logged | Report this post to a Moderator
minerva
LymeNet Contributor
Member # 20410

Icon 1 posted      Profile for minerva     Send New Private Message       Edit/Delete Post   Reply With Quote 
i had this done and my doc didn't use lab corp and we got a breakdown with to many numbers and my doc didn't really know how to read it, so not only did i pay my 20% it took forever and i am no futher ahaead.

just a heads up. labcorp is the one you want.

Posts: 161 | From sonoma county | Registered: May 2009  |  IP: Logged | Report this post to a Moderator
ktkdommer
Frequent Contributor (1K+ posts)
Member # 29020

Icon 1 posted      Profile for ktkdommer     Send New Private Message       Edit/Delete Post   Reply With Quote 
My doctor said I needed to have CD-57's done at LabCorp. Insurance doesn't cover it because it is too new and is considered experimental. If I self paid right up front it was $153. If I would have tried to bill it through insurance and they didn't cover it, the cost to me then would be over $200. Lucky me, I got to pay for 3 of the tests in different months.
My youngest was 48, I'm 80 and my oldest is 100. The doctor wants us to be 150 before discontinuing treatment.

--------------------
Things are never dull. After 3 fighting Lyme, 2 are in remission. Youngest is still sick, age 22. He has new diagnosed Chiari Malformation and Ehlers Danlos Syndrome.

Posts: 1366 | From Perrysburg, Ohio | Registered: Nov 2010  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.