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 » EBV reference help

 - UBBFriend: Email this page to someone!    
Author Topic: EBV reference help
KentuckyWoman
LymeNet Contributor
Member # 38894

Icon 1 posted      Profile for KentuckyWoman     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am trying to find where I read somewhere, either on here or in "Cure Unknown" about how patients with Lyme will test positive for EBV. I did test + last year for EBV, but would like to find that reference.
Help Anyone??

--------------------
KentuckyWoman
tired of medical run-arounds

Two roads diverged in a wood, and I, I took the one less traveled by,
And that has made all the difference.
~ ~ Robert Frost

Posts: 221 | From Kentucky | Registered: Sep 2012  |  IP: Logged | Report this post to a Moderator
minimonkey
LymeNet Contributor
Member # 8693

Icon 1 posted      Profile for minimonkey     Send New Private Message       Edit/Delete Post   Reply With Quote 
My LLMD told me that Lyme reactivates EBV -- and my EBV antibodies are off the charts (literally) every time I've had them tested --

Valtrex helped immensely with a lot of my symptoms.

I am fairly certain I've read reference to this somewhere, too, but I don't remember where.

--------------------
"Looks like freedom but it feels like death..
It's something in between, I guess"

Leonard Cohen, from the song "Closing Time"

Posts: 822 | From California | Registered: Jan 2006  |  IP: Logged | Report this post to a Moderator
Haley
Frequent Contributor (1K+ posts)
Member # 22008

Icon 1 posted      Profile for Haley     Send New Private Message       Edit/Delete Post   Reply With Quote 
My doctor doesn't even test for EBV as he says everyone has it.
Posts: 2232 | From USA | Registered: Aug 2009  |  IP: Logged | Report this post to a Moderator
Ellen101
Frequent Contributor (1K+ posts)
Member # 35432

Icon 1 posted      Profile for Ellen101     Send New Private Message       Edit/Delete Post   Reply With Quote 
I believe I heard that most people would test positive for EBV as well. What is important is if the virus is active or not.

minimonkey what symptoms did valtrex help you with?

Posts: 1748 | From United States | Registered: Dec 2011  |  IP: Logged | Report this post to a Moderator
KentuckyWoman
LymeNet Contributor
Member # 38894

Icon 1 posted      Profile for KentuckyWoman     Send New Private Message       Edit/Delete Post   Reply With Quote 
ah, thanks you all. I think i get it now. I somehow had it in my dizzy head that EBV positives were really somehow not nec EBV, but Lyme showing up in that way.

I know.. I know.. I'm a goober.

At least that explains my test last year.. I thought I'd had mono as a teen, but then it showed up last year as if THAT was the "diagnosis" for my lethargy, etc.

--------------------
KentuckyWoman
tired of medical run-arounds

Two roads diverged in a wood, and I, I took the one less traveled by,
And that has made all the difference.
~ ~ Robert Frost

Posts: 221 | From Kentucky | Registered: Sep 2012  |  IP: Logged | Report this post to a Moderator
timaca
Frequent Contributor (1K+ posts)
Member # 6911

Icon 1 posted      Profile for timaca     Send New Private Message       Edit/Delete Post   Reply With Quote 
This may help you: http://chronicfatigue.stanford.edu/infections/herpes.html

Read all the sections under the Herpes Virus sections. Also, check out some of the publications on this page: http://chronicfatigue.stanford.edu/infections/herpes-research.html

Best, Timaca

Posts: 2872 | From above 7,000 ft in a pine forest | Registered: Feb 2005  |  IP: Logged | Report this post to a Moderator
KentuckyWoman
LymeNet Contributor
Member # 38894

Icon 1 posted      Profile for KentuckyWoman     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thank You timaca, that did help to explain some things.

--------------------
KentuckyWoman
tired of medical run-arounds

Two roads diverged in a wood, and I, I took the one less traveled by,
And that has made all the difference.
~ ~ Robert Frost

Posts: 221 | From Kentucky | Registered: Sep 2012  |  IP: Logged | Report this post to a Moderator
BuffyFan
LymeNet Contributor
Member # 34679

Icon 1 posted      Profile for BuffyFan     Send New Private Message       Edit/Delete Post   Reply With Quote 
so if it's not active no treament?
Posts: 287 | From somewhere | Registered: Oct 2011  |  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 
My non-lyme specialist doc tells me EBV is one of those that's just everywhere, we've all got some here and there, with chronic immune suppression (such as with lyme), then naturally it would be more active. It's one he doesn't bother to treat specifically, but rather works on immune support generally.
Posts: 1927 | From se usa | Registered: Mar 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.