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 » Lyme and MS

 - UBBFriend: Email this page to someone!    
Author Topic: Lyme and MS
takethat89
Member
Member # 45625

Icon 1 posted      Profile for takethat89     Send New Private Message       Edit/Delete Post   Reply With Quote 
I wondered if anyone would think it was worth seeing a neurologist to rule out stuff like MS. I read someone else in a group who believes they are two different things and treating for lyme with MS can cause huge problems and vice versa seems the treatments are boosting the immune system (lyme), vs suppressing it (MS)...but what if you had both? Thoughts? I have tested positive for lyme on igenex
Posts: 53 | From Texas | Registered: Apr 2015  |  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 could be dangerous to treat for "MS" if you really have Lyme. It may cause you to never be able to recover from the Lyme.

Treating for Lyme first will most likely fix the "MS." MS is a diagnosis of exclusion. There is no definitive test for it.

If I'm not mistaken, every single ALS patient who has been tested for Lyme has been found to have it. My thinking is that the same would be true for MS .. given that the testing was from a reliable lab and the results interpreted by a doctor who actually knows something about Lyme.

PS .. Neurologists are terrible at finding Lyme. For one thing, they think one must do a spinal tap and if it's negative, then everything is fine.

Nothing could be further from the truth. The spinal tap is about 20% accurate at finding Lyme.

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

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
takethat89
Member
Member # 45625

Icon 1 posted      Profile for takethat89     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for the response. Would this not be true then in treating for lyme when you also have mS if the two are in fact different things? Or if you had both. It is all confusing i guess. I think igenex testing is pretty reliable though? I am about to start lyme treatment and i have never been checked for MS, so i guess i get anxious thinking what if i have MS and lyme treatment actually makes me worse.
Posts: 53 | From Texas | Registered: Apr 2015  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=117839;p=0

Topic: Could (misdiagnosed) MS be Lyme?

Many links here about the Lyme-MS connection

Also be sure to watch the film: UNDER OUR SKIN
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
Be aware that steroids are often used to treat "MS" - why that can be so very devastating for a very long time for anyone with lyme:

http://flash.lymenet.org/scripts/ultimatebb.cgi/topic/1/100984?#000000

Topic: what do STEROIDS actually do to those with lyme? Risks, long term damage discussed. Links.
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  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 
I don't see any reason that treating for Lyme would make MS worse.

Which MS symptoms do you think you have?

Be sure to read the thread that Keebler posted .. the first link above.

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

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
project
LymeNet Contributor
Member # 46200

Icon 1 posted      Profile for project     Send New Private Message       Edit/Delete Post   Reply With Quote 
You might want to also take a look at http://cpnhelp.org/
There are a lot of MS patients on there. They are focused on eliminating the Chlamydia Pneumonia bacteria rather than Borrelia but some have reversed their diagnosed "MS" by taking antibiotics long-term. However their antibiotic protocol would probably kill other pathogenic bacteria like Borrelia too. It's likely most of these neurodegenerative conditions have some infectious component.

Posts: 131 | From CO | Registered: Jul 2015  |  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.