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 » Cash Labs=Frustration

 - UBBFriend: Email this page to someone!    
Author Topic: Cash Labs=Frustration
abhistbuff
Member
Member # 28230

Icon 8 posted      Profile for abhistbuff     Send New Private Message       Edit/Delete Post   Reply With Quote 
Has anyone else out there been frustrated by labs that are "cash only" and will not bill your insurance? For example...My last LLMD who said he wanted to test for magnesium by scraping skin cells inside my mouth instead of doing blood work? 290 dollars instead of it being covered completely. Has anyone else been annoyed with such tests? Do Lyme patients have the right to ask questions about such things? Or should we just sit back while our bank accounts are drained?
Posts: 63 | From dc | Registered: Sep 2010  |  IP: Logged | Report this post to a Moderator
Carol in PA
Frequent Contributor (5K+ posts)
Member # 5338

Icon 1 posted      Profile for Carol in PA     Send New Private Message       Edit/Delete Post   Reply With Quote 
Although the lab will not submit the bill to insurance, I think that you can.
You may need to call around to get the right form to use.

The blood test for magnesium might be covered by insurance, but what good is it if it doesn't give the information that you need?

Are you taking mag supplements and eating foods high in magnesium?

Posts: 6947 | From Lancaster, PA | Registered: Feb 2004  |  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 
A lot of this stuff my insurance won't cover. My LLMD knows that I need the best way and covered way to test. He usually lets me make a choice understanding that there are 3 of us. Some testing I will pay out of pocket for and sometimes it is only for my sickest child.

My sister is sick and out of work so she questions almost everything. Her doctor I think knows it comes with the territory. Her insurance is horrible.

It is frustrating when you can't get what your doctor tells you you need to get well.

I'm sure your doctor knows the difference in the magnesium testing and what might give him more diagnostic data. I would ask.

--------------------
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
Fuel1212
LymeNet Contributor
Member # 29312

Icon 1 posted      Profile for Fuel1212     Send New Private Message       Edit/Delete Post   Reply With Quote 
Its nearly impossible to find a deficiency in mag with a standard blood test.

I think he knows what he is doing..

Make sure you submit to your ins to see if they will cover at least part of it. Ask your doctor to use a routine code.... seems to help me


Fuel

--------------------
IgM- 31,34,39,83-93 IND
IgM- 41+

IgG- 31,34,39,83-93 IND
IgG- 41++

Posts: 610 | From Lymeville | Registered: Nov 2010  |  IP: Logged | Report this post to a Moderator
abhistbuff
Member
Member # 28230

Icon 1 posted      Profile for abhistbuff     Send New Private Message       Edit/Delete Post   Reply With Quote 
I do consume foods high in magnesium and take supplements. When it comes to cash labs I have been shocked to learn that:

A doctor can be the owner of the lab himself. (that will not take insurance)

There are many tests that evaluate adrenals, nutrition, etc that are available to the medical community and covered by many insurance carriers.

Mine will only reject a claim if the test is available from a mainstream lab already.

Posts: 63 | From dc | Registered: Sep 2010  |  IP: Logged | Report this post to a Moderator
scorpiogirl
Frequent Contributor (1K+ posts)
Member # 31907

Icon 1 posted      Profile for scorpiogirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yep ALL my tests and now my daughter's test were cash up front. Mine exceeded $5,000 and hers were close to $3,000. Lab Corp was the only place that took insurance!

I'm finding out this week that the Compounding Pharmacies don't accept insurance either! So my B 12, cholestyramine, etc... are also cash upfront. I have yet succeed in getting my insurance to reimburse me for this... nor did they pay for my Bicillin. Sooo FRUSTRATING!!

Lyme is definitely a rich man's disease!!

--------------------
 -

Posts: 1391 | From Lyme Land | Registered: May 2011  |  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.