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 » L'Hermitte's and Lyme

 - UBBFriend: Email this page to someone!    
Author Topic: L'Hermitte's and Lyme
patsmad
Member
Member # 9178

Icon 1 posted      Profile for patsmad     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hey, can someone tell me if L'Hermitte's sign (buzzing/zapping down the spine when neck is bent forward) can be associated with Lyme Disease? I have had this for 10 months along with other "classic" MS symptoms, and I am desperately hoping for Lyme Disease (I had a test done at IGeneX and I'm still considered "negative", with only four positive points & two that were IND). No evidence of MS, either, so I'm in limbo. Also, I'm taking Doxycycline orally - can this be effective even for neuro-Lyme?
Thanks.

Posts: 23 | From wyoming | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
Bluetick
Member
Member # 8467

Icon 1 posted      Profile for Bluetick     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have that symptom. LLMD and non-LL neurologist told me that it is caused by lyme and/or MS.

MS is basically a symptom, not really a diagnosis. The term 'multiple sclerosis' just means multiple areas of demyelination in the CNS and can be used to describe these symptoms caused by lyme disease.

My LLMD believes that MS is lyme disease.

[ 13. May 2006, 03:05 PM: Message edited by: Bluetick ]

Posts: 98 | From MA | Registered: Dec 2005  |  IP: Logged | Report this post to a Moderator
dontlikeliver
Frequent Contributor (1K+ posts)
Member # 4749

Icon 1 posted      Profile for dontlikeliver     Send New Private Message       Edit/Delete Post   Reply With Quote 
I had L'hermittes 7 years ago. It can be caused by any inflammation as far as I know, it is not exclusive to MS.
Posts: 2824 | From The Back of Beyond | Registered: Oct 2003  |  IP: Logged | Report this post to a Moderator
Reno'sBack
LymeNet Contributor
Member # 7367

Icon 6 posted      Profile for Reno'sBack     Send New Private Message       Edit/Delete Post   Reply With Quote 
Bluetick, Yay!!! I found you! [Big Grin] Do you see Dr.P?

Do you know the others with demyelination? I'm not online enough.

Thanx~Reno

--------------------
~Life's too short, eat dessert first

Posts: 134 | From PA | Registered: May 2005  |  IP: Logged | Report this post to a Moderator
Bluetick
Member
Member # 8467

Icon 1 posted      Profile for Bluetick     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Reno,

Yup, I see Dr. P. I know of a few people on here with demyelination and lyme disease.

I hope that you are doing well with treatment.

Bluetick

Posts: 98 | From MA | Registered: Dec 2005  |  IP: Logged | Report this post to a Moderator
TheCrimeOfLyme
Frequent Contributor (1K+ posts)
Member # 4019

Icon 1 posted      Profile for TheCrimeOfLyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
Ive had it ever since I was in my early teens, so about for 13 years.

--------------------
You want your life back? Take it.

Posts: 3169 | From Greensburg, Pennsylvania | Registered: Jun 2003  |  IP: Logged | Report this post to a Moderator
patsmad
Member
Member # 9178

Icon 1 posted      Profile for patsmad     Send New Private Message       Edit/Delete Post   Reply With Quote 
You've had it for 13 years - I'm assuming you don't have MS? Have you been treated for Lyme, and if so, do you know why you still have L'hermitte's?
Posts: 23 | From wyoming | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
BOEJR
LymeNet Contributor
Member # 1734

Icon 1 posted      Profile for BOEJR     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Patsmad,

Are you having your testing done while you are activily on Abx? This would make a substantial difference in the results.

Just a thought.

Julia

--------------------
Please consult your LLMD before making any changes to your treatment regimen.

Posts: 641 | From NJ, USA | Registered: Oct 2001  |  IP: Logged | Report this post to a Moderator
patsmad
Member
Member # 9178

Icon 1 posted      Profile for patsmad     Send New Private Message       Edit/Delete Post   Reply With Quote 
No, I wasn't on antibiotics when I was tested for Lyme.
Posts: 23 | From wyoming | Registered: May 2006  |  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 
I developed L'Hermittes last year -- shortly before I was diagnosed with Lyme. Ducks were trying to go down the MS road with me, but the overall clinical picture was clearly more lyme than MS. MRI of CSpine ruled out disc problems, etc.

I came back CDC positive for Lyme, and the L'Hermittes was one of the first symptoms to disappear with abx treatment.

--------------------
"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
   

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.