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 » Dr. B mentions Borna Virus in recent lecture...anyone know anything about it?

 - UBBFriend: Email this page to someone!    
Author Topic: Dr. B mentions Borna Virus in recent lecture...anyone know anything about it?
tick battler
Frequent Contributor (1K+ posts)
Member # 21113

Icon 1 posted      Profile for tick battler     Send New Private Message       Edit/Delete Post   Reply With Quote 
Has your LLMD mentioned borna virus? If so, what was said about it? Any recommended treatments?

I noticed borna virus is something new that Dr. B didn't mention when I heard him lecture 2 years ago.

I expect we will hear more about it down the road.

Thanks,

tickbattler

Posts: 1763 | From Malvern, PA | Registered: Jul 2009  |  IP: Logged | Report this post to a Moderator
seibertneurolyme
Frequent Contributor (5K+ posts)
Member # 6416

Icon 1 posted      Profile for seibertneurolyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hubby was diagnosed with Borna Virus back in 2002 I think. He has been on the antiviral med Amantadine ever since. It has not really worked -- tested positive for Borna Virus a total of 4 times I think in total over 2 or 3 years. Unfortunately there are currently no labs which can test for this virus in the U.S. There is a test available in Germany, but we have not had the funds to have that test done.

Valtrex is another med possibility I think. But it is fairly expensive. Hubby's docs have never been very interested in pursuing viral issues and I know at some point that may need to be addressed.

If you do a search here on LymeNet there are a few threads I have posted over the years, but there has been very little research done on this virus since it was first discovered in humans. Lots of initial interest since it was found mostly in schizophrenic patients.

I am pretty sure Borna Virus was discussed at one of the Lyme conferences in the last year or two. Dr B didn't really know anything about it back in 2003 when hubby was his patient and had had a couple of positive tests at that time.

Bea Seibert

Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
jkmom
LymeNet Contributor
Member # 14004

Icon 1 posted      Profile for jkmom     Send New Private Message       Edit/Delete Post   Reply With Quote 
My daughter did the German borna virus test and was positive.

Her LLMD put her on Valtrex. He said he had seen bad things happen to his adult patients on Amantadine. The German lab used Amantadine in their studies.

My daughter got very giggly (in a good way) the first few days on the Valtrex. That wore off and she started having balance problems.

When I picked up the Valtrex for the second month, I noticed a side effect of Valtrex was balance problems. I asked the pharmacist about this and surprisingly, he said the balance problems were probably caused by die off of the virus.

She got bad enough that she couldn't really walk without help so we took her off to see what would happen. Her balance problems cleared up.

Her LLMD thinks she does need to do the Valtrex at some point, but we aren't doing it now.

Posts: 984 | From US | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
tick battler
Frequent Contributor (1K+ posts)
Member # 21113

Icon 1 posted      Profile for tick battler     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for the responses.

Bea - how was your husband diagnosed? You said you didn't get the German test done. Is there a test here that you did?

tickbattler

Posts: 1763 | From Malvern, PA | Registered: Jul 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.