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 » XMRV testing?

 - UBBFriend: Email this page to someone!    
Author Topic: XMRV testing?
jackie81
LymeNet Contributor
Member # 27031

Icon 1 posted      Profile for jackie81     Send New Private Message       Edit/Delete Post   Reply With Quote 
Does anyone know where you can get XMRV testing done? Also, is it available to Canadians?
Posts: 574 | From Out there somewhere | Registered: Jul 2010  |  IP: Logged | Report this post to a Moderator
Mariski
Member
Member # 24942

Icon 1 posted      Profile for Mariski     Send New Private Message       Edit/Delete Post   Reply With Quote 
The Whittemore Peterson Insitute -- which is where connection between the XMRV retrovirus and CFS was discovered -- recommends that you have the testing done here:

http://www.vipdx.com/order/

The tests are quite comprehensive, as they now include both XMRV and other human MLV-related viruses.

They tests can be done using just blood serum, or culture, or both.

Your doctor needs to set up the account. I assume that it would be available to Canadians, but I am not sure.

Posts: 40 | From New York | Registered: Mar 2010  |  IP: Logged | Report this post to a Moderator
mcaringella
LymeNet Contributor
Member # 24848

Icon 1 posted      Profile for mcaringella   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
My doctor is doing it thru a local university grant study. I'm in southern california. Let me know if you want more info and I'll PM you.

--------------------
Blessings to you!

Posts: 141 | From Southern California | Registered: Mar 2010  |  IP: Logged | Report this post to a Moderator
jackie81
LymeNet Contributor
Member # 27031

Icon 1 posted      Profile for jackie81     Send New Private Message       Edit/Delete Post   Reply With Quote 
I do want more info but I am wondering if Canadians can participate?
Posts: 574 | From Out there somewhere | Registered: Jul 2010  |  IP: Logged | Report this post to a Moderator
maritzap
Member
Member # 11146

Icon 1 posted      Profile for maritzap     Send New Private Message       Edit/Delete Post   Reply With Quote 
Is your doctor in southern CA also? I am in San Diego and am interested in this test for my daughter. can you pm me please if you can't share publicly the university study info.
Thank you!

Posts: 75 | From San Diego, CA | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
baileypup
LymeNet Contributor
Member # 22824

Icon 1 posted      Profile for baileypup     Send New Private Message       Edit/Delete Post   Reply With Quote 
I would also like the info, and am in So Cal/San Diego area. Can you please pm the university grant study info.

Is this Dr. B. in OC, and if not, what doctor do you see?

Posts: 964 | From san diego | Registered: Oct 2009  |  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.