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 » tularemia

 - UBBFriend: Email this page to someone!    
Author Topic: tularemia
focusonsurvival
Member
Member # 9124

Icon 1 posted      Profile for focusonsurvival     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am wondering what kinds of treatments people have tried for tularemia and what the results were like? I have been on Levaquin. Doesn't seem to have helped much. I also wanted to know what kinds of symptoms people have had from Tularemia - although it may be hard to distinguish from Lyme. thanks, focus
Posts: 55 | From Mamaroneck, New york | Registered: Apr 2006  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
It's strange, but we rarely have anyone here who has been dxd with it. Dont' know why. Have you been checked for all the other diseases a tick might have given you?

Did you get tularemia from a tick?

You can do a search here by clicking on the little word "search" in the upper portion of this page. I just did that and came up with several links.

Here's one of them:
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=037225

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
focusonsurvival
Member
Member # 9124

Icon 1 posted      Profile for focusonsurvival     Send New Private Message       Edit/Delete Post   Reply With Quote 
I mean of course even if with the Lyme I never saw the tick, but believe I got if from a tick. So the answer is yes, I got tularemia from a tick. I know there are others who have this co-infection, according to Dr. B and just wanted someone to share if they have had this too.
Thanks, Focus

Posts: 55 | From Mamaroneck, New york | Registered: Apr 2006  |  IP: Logged | Report this post to a Moderator
Jill E.
Frequent Contributor (1K+ posts)
Member # 9121

Icon 1 posted      Profile for Jill E.     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Focus,

Can you tell me which lab you used for a Tularemia test? When I first was diagnosed with Lyme/coinfections, I asked my LLMD if there was a test for Tularemia because there have been confirmed cases in wild rabbits near me, and the darn tick that bit me gave me everything else...he said the tick could have given me Tularemia but he wasn't aware of tests or treatment. I'd appreciate any info because I'm concerned it could be one more disease that's being overlooked.

Thanks,
Jill

--------------------
If laughter is the best medicine, why hasn't stand-up comedy cured me?

Posts: 1773 | From San Diego | Registered: Apr 2006  |  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 
Jill,

Google search located this test kit.

http://www.nhdiag.com/tularemia.shtml

Bea Seibert

Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004  |  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 
Found a very thorough article on this. Lots of info as Tularemia is considered a biological weapon.

http://www.emedicine.com/emerg/topic591.htm

Seem to be several choices of antibiotics. No idea as to effectiveness.

Bea Seibert

Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
Jill E.
Frequent Contributor (1K+ posts)
Member # 9121

Icon 1 posted      Profile for Jill E.     Send New Private Message       Edit/Delete Post   Reply With Quote 
Bea,

Thanks so much for both links. I'm going to print all this out and bring it to my LLMD.

Jill

--------------------
If laughter is the best medicine, why hasn't stand-up comedy cured me?

Posts: 1773 | From San Diego | Registered: Apr 2006  |  IP: Logged | Report this post to a Moderator
elle
LymeNet Contributor
Member # 7721

Icon 1 posted      Profile for elle     Send New Private Message       Edit/Delete Post   Reply With Quote 
LabCorp has stopped offering the test for tularemia.

It is available at Quest.


elle

--------------------
When I feel blue . . . . . . its time to take another breath

Posts: 296 | From East Coast | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
focusonsurvival
Member
Member # 9124

Icon 1 posted      Profile for focusonsurvival     Send New Private Message       Edit/Delete Post   Reply With Quote 
Quest was where I got my test done.
Posts: 55 | From Mamaroneck, New york | Registered: Apr 2006  |  IP: Logged | Report this post to a Moderator
Jill E.
Frequent Contributor (1K+ posts)
Member # 9121

Icon 1 posted      Profile for Jill E.     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks - there used to be a Quest near me but several labs merged. If not still there, I know there are Quests in Los Angeles.

I appreciate the testing info.

Jill

--------------------
If laughter is the best medicine, why hasn't stand-up comedy cured me?

Posts: 1773 | From San Diego | Registered: Apr 2006  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Quest is lousy for all the other tests. I wouldn't depend on it to find anything. They have alot of false negatives.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96239 | From Texas | Registered: Feb 2001  |  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.