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 » WHICH Ingenex/MDLab tests to do?

 - UBBFriend: Email this page to someone!    
Author Topic: WHICH Ingenex/MDLab tests to do?
duramater
LymeNet Contributor
Member # 6480

Icon 5 posted      Profile for duramater     Send New Private Message       Edit/Delete Post   Reply With Quote 
In a phone consult with my old LLMD, he suggested I have my PCP do some tests from Ingenex & MDlab - Lyme stuff and other tick illnesses. I want to bring the forms to my doc next week.

I went to the two websites to get the forms and sample instructions: Crud city! There are a bajillion tests on these forms. So exactly which ones did your doc do???

A bit of background if this should help:

I've had regular ELISAs before be positive, blood and CSF. But this time around (I'm sick again), nada. Even had PCRs on blood and CSF this time. Bupkiss. All they will give me without a positive test is doxy which isn't working (I'm bed-bound with neuro & cardiac symptoms and pancreatitis too - related???). Because I am so weak and ill, I can't make it to the LLMD because it is too far. So this route is the best thing to do right now.

So what are the best tests to order off these forms? Also, because I was sick so many years ago before they knew about these other related illnesses, I've not been tested.

So, if you could list the tests that were done on your Ingenex &/or MDLabs results, that would help a ton. If I don't do the forms, I think my doc will be too overwhelmed to know what to order.

Thanks a bunch folks.


Posts: 689 | From western MA (we say buttER and pizzA) | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
duramater
LymeNet Contributor
Member # 6480

Icon 1 posted      Profile for duramater     Send New Private Message       Edit/Delete Post   Reply With Quote 
Up for some help; dig out those test results folks and read me the tests done! Thanks.
Posts: 689 | From western MA (we say buttER and pizzA) | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
minoucat
Frequent Contributor (1K+ posts)
Member # 5175

Icon 1 posted      Profile for minoucat     Send New Private Message       Edit/Delete Post   Reply With Quote 
For Bb, we did the Igenex Western Blot IgG and IgM. The hubby was positive on both; I'm hardly ever positive on anything.

For babs, the hubby did the Igenex Babs PCR specific to WA-1 (very important to check for the right strain, which is related to where you think you were infected. Didn't come up with a positive, which is not unusual for PCRs. The FISH wasn't available then; I understand that it's a much better test for babs. But he was so symptomatic for babs that the LLMD treated anyway.

Didn't test for bart, treated based on sx.

Checked for mycoplasma and black fungus using the darkfield microscope. Positive for both.

Having said all that -- can't your LLMD at least tell you what tests he'd want to have run? Seems kind of cold to expect you to come up with this yourself.

Failing everything else, how about you contact whatever lab you want to use and see what tests the physicians are requesting for cases like yours? Igenex.com and mdl.com, I believe.

There's also the Bowen Lab, which I've never used; if you're looking for something that will force your PCP or your insurance to fork over treatment, I don't know if Bowen has enough credibility with the powers that be for their results to be useful.


Posts: 2331 | From WA | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
bg
Junior Member
Member # 46416

Icon 1 posted      Profile for bg     Send New Private Message       Edit/Delete Post   Reply With Quote 
DM,

I had WESTERN BLOT IGM & IGG done on myself & hubby. These 2 tests cost $180; $90 each. If you have them bill you, it's an extra $40...

I'm POSITIVE on both; he had some positives but not enough to be declared positive.

IGENEX does NOT handle insurance so it's PREPAY by check/credit card!

I submited IGX paid bill to Iowa's BC/BS, which sent to BLUE CARD Calif. I was reimbursed only $43 since IGX is NOT on approved list of labs BC deals with!

MD & BOWEN both accept MOST insurances they told me.

Whoever does your test, make sure their form was SIGNED BY DR. & HAS A DIAGNOSIS ON.

On their form, write you want results FAXED to your dr. and paper copy sent there. Mine were lost after IGX sent for about 5 wks.

Good luck! Betty G.

Not sure ... did you try Treepatrol/tincup's newbie links to see what they might have about testing also?


Posts: 1 | From US | Registered: Aug 2015  |  IP: Logged | Report this post to a Moderator
riversinger
Frequent Contributor (1K+ posts)
Member # 4851

Icon 1 posted      Profile for riversinger   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Igenex accepts Medicare, with proper ICD-9 codes. MDL accepts Medicare and other insurance. Bowen is not allowed to accept any insurance.

With Igenex, I had Lyme Western Blot and the Dot Blot Urine Antigen test following an antibiotic challenge.

For Babesia, the WA-1 antibody, B. Microti antibody IgM and IgG, Babesia FISH, Babesia PCR on whole blood.

For Ehrlichia, PCR for HME and HGE on serum, IgG and Igm antibody for HME and HGE.

Some of these were probably done as panels, but I can't tell from the tests. I also was tested for Bartonella, but can't find which test it was.

I was positive for Lyme and HME. My doctor thinks I have Babesia in spite of negative tests.

Make sure, whatever you test for, that your doctor provides you with diagnosis codes (ICD-9.) They are required for any kind of insurance re-imbursement.

------------------
Sonoma County Lyme Support
[email protected]


Posts: 2142 | From California | Registered: Nov 2003  |  IP: Logged | Report this post to a Moderator
duramater
LymeNet Contributor
Member # 6480

Icon 1 posted      Profile for duramater     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hey folks,

thanks for info to date. river, as i have medicare, i'll be submitting directly to ingenex and mdlab w/o pre-pay.

i know the code for lyme (oh so well) but does the doc have to use codes for the other diseases if we are only ruling them out?

can you tell me what codes were used on your paperwork if you have access to it?

many thanks to all for their effort

~DM


Posts: 689 | From western MA (we say buttER and pizzA) | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
riversinger
Frequent Contributor (1K+ posts)
Member # 4851

Icon 1 posted      Profile for riversinger   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I think you do have to use the individual codes, especially for Medicare. They are very particular. I'm sorry, I don't know the codes for anything but Lyme. Can't your doctor's office look these up for you?

The diagnosis codes aren't printed out on the lab results. If necessary, you can look up ICD-9 codes on the web.

------------------
Sonoma County Lyme Support
[email protected]


Posts: 2142 | From California | Registered: Nov 2003  |  IP: Logged | Report this post to a Moderator
ArtistDi
Frequent Contributor (1K+ posts)
Member # 2297

Icon 1 posted      Profile for ArtistDi     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi. I see you are in Western MA--my area of
the country. There is a doctor here who
is lyme sympathetic and can do your blood work for Igenex or MDL. Has kits in his office.

Email me and I will give you his name and
number.

[This message has been edited by ArtistDi (edited 31 January 2005).]


Posts: 1572 | From Hatfield, MA, USA | Registered: Mar 2002  |  IP: Logged | Report this post to a Moderator
bg
Junior Member
Member # 46416

Icon 1 posted      Profile for bg     Send New Private Message       Edit/Delete Post   Reply With Quote 
Riversinger,

You mentioned the dx code. The dr. puts the code of what HE/SHE thinks you might have, and it's NOT lyme!

So from what I have learned, you don't show the lyme dx there since lyme HAS NOT been confirmed/dx. The dr. must furnish the code of his choice.

Drs. office did not put a dx code on mine going to IGX, and put a really wrong code on my husbands! He has essential tremors and they showed Lewy body disease! someone screwed up royally. Betty G.


Posts: 1 | From US | Registered: Aug 2015  |  IP: Logged | Report this post to a Moderator
riversinger
Frequent Contributor (1K+ posts)
Member # 4851

Icon 1 posted      Profile for riversinger   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Betty,

Actually, if they are testing for Lyme, they do have to put the Lyme code, at least if you want to get paid. I know this for a fact, because my insurance sends it back unpaid with no dx code, and if it isn't the code for what they are testing, or something related, they also won't pay.

I just sent two sets of labs out with the dx of Chlamaydia psitacci. My doctor doesn't know if I have it, but that is what we are trying to find out. It seems screwy to me, but that is how it works.

------------------
Sonoma County Lyme Support
[email protected]


Posts: 2142 | From California | Registered: Nov 2003  |  IP: Logged | Report this post to a Moderator
ElizabethP
Member
Member # 6819

Icon 1 posted      Profile for ElizabethP     Send New Private Message       Edit/Delete Post   Reply With Quote 
ArtistDi,

I'm also in W. MA - tried e-mailing you to get the info on the MD who works with IGenex & MDL but it was returned. Any chance you can e-mail me with the info?

Thanks!


Posts: 27 | Registered: Jan 2005  |  IP: Logged | Report this post to a Moderator
minoucat
Frequent Contributor (1K+ posts)
Member # 5175

Icon 1 posted      Profile for minoucat     Send New Private Message       Edit/Delete Post   Reply With Quote 
DM, your email to me got eaten by the ether rats. Lost the message and your addy. Please resend. Cheers, m
Posts: 2331 | From WA | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
Paisley
LymeNet Contributor
Member # 6502

Icon 1 posted      Profile for Paisley     Send New Private Message       Edit/Delete Post   Reply With Quote 
if you are still in need code (s) for which tests let me know ...i have the kits for my pcp blood draw ...ther were quite a few tests my llmd ordered...haven't had my blood draw yet.
Posts: 298 | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
MammaLyme
Frequent Contributor (1K+ posts)
Member # 1257

Icon 3 posted      Profile for MammaLyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
Get the Bowen test www.bowen.org
The test is $250 as a donation and they recently received their patent for this test. They are waiting for FDA approval. This tests shows all the babesia and HME and HGE. I went to 16 doctors from 1994 when bitten until 2000 when I got a positive lyme from the LUAT test. Then I had the PCR from Igenex which only showed lyme. In 2001 a doctor had a presentation showing the Bowen tests and stated you can see the spiroketes waving back at you. I also had a positive Elisa from Quest; MDL was worthless and showed nothing; BBI showed babs only no lyme; band 41 from a Quest WB. Then my regular doctor let me go to Bowen.
SAVED MY LIFE. I not only had the pictures to show lyme but babesia, HME and HGE. No wonder I had gone to 16 different doctors who said I had MS, Lupus etc.
I no have no coinfections at all but still have medium lyme count. It did go all the way down to 1:4 when I really felt good. My husband is getting another test in two weeks after being on an IV for 5 months and then KETEK.
Bowen can see all of the babesia not just WA-1 and Microti.
Get well. Get this test.

Posts: 2173 | From Maryland | Registered: Jun 2001  |  IP: Logged | Report this post to a Moderator
duramater
LymeNet Contributor
Member # 6480

Icon 1 posted      Profile for duramater     Send New Private Message       Edit/Delete Post   Reply With Quote 
Paisely!

YES PLEASE post codes -- I'm going to try to contact labs today, but all help is SO welcome in case I can't make the calls for whatever reason. Doc appt on FRIDAY.

Many thaks

~DM


Posts: 689 | From western MA (we say buttER and pizzA) | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
duramater
LymeNet Contributor
Member # 6480

Icon 1 posted      Profile for duramater     Send New Private Message       Edit/Delete Post   Reply With Quote 
Up for Paisley help.
Posts: 689 | From western MA (we say buttER and pizzA) | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
Paisley
LymeNet Contributor
Member # 6502

Icon 1 posted      Profile for Paisley     Send New Private Message       Edit/Delete Post   Reply With Quote 
i need to get back to you in a few hours - i'll get it for you !
Posts: 298 | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
Paisley
LymeNet Contributor
Member # 6502

Icon 1 posted      Profile for Paisley     Send New Private Message       Edit/Delete Post   Reply With Quote 
duramater...do you have an email so I can get these to you?
Posts: 298 | Registered: Nov 2004  |  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.