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 » Why is this not used for Lyme treatment?

 - UBBFriend: Email this page to someone!    
Author Topic: Why is this not used for Lyme treatment?
IrTabby2
Member
Member # 31079

Icon 1 posted      Profile for IrTabby2     Send New Private Message       Edit/Delete Post   Reply With Quote 
So currently I have no immune system and am

very ill. Doing some research on here concerning

virus's and their effect on us, I read a comment

"Until we can learn how to fix our immune system

we need to treat the pathogens".


This really made me think because currently my

stepmother is undergoing chemo therapy for breast

cancer. And along with the chemo she is given

these shots which are basicly super powered

immune-system boosters.

To my logic if there is a medicine out there

that can super charge our immune system, why is

it not being used in the treatment of people with

LD or different virus's, when current treatments

are so inferior?

Posts: 34 | From NJ | Registered: Mar 2011  |  IP: Logged | Report this post to a Moderator
scorpiogirl
Frequent Contributor (1K+ posts)
Member # 31907

Icon 1 posted      Profile for scorpiogirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
The answer is simple, because they still don't believe that there is chronic lyme and that there is no way we all could be this sick!! Why fix something they don't believe we have?

--------------------
 -

Posts: 1391 | From Lyme Land | Registered: May 2011  |  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 
It is not quite that simple. If your immune system is overactive then you risk developing an autoimmune disease and possibly permanent nerve damage.

Also if you have bart it is probably suppressing your immune system in a major way and you may have no idea just what all you are infected with.

We think hubby has finally gotten rid of his bartonella or mycoplasma or BLO or whatever the mystery pathogen was. But now he has a new problem -- he is trying to treat babesia aggressively.

As a result when his red blood cells burst (hemolysis) his white blood count goes up and he runs very high fevers. He has been diagnosed with bacteremnia by blood cultures 2 times and has been hospitalized 4 times in the last 9 weeks with high fevers.

The normal 10 days of antibiotics for his specific bacteria have not worked as they should. His immune system almost seems to be working too well to identify the bacteria but it is not working to kill the bacteria.

This is just one example of how the immune system can be both under and over active and dysfunctional.

Bea Seibert

Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
IrTabby2
Member
Member # 31079

Icon 1 posted      Profile for IrTabby2     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thats an interesting way of lookint at it Bea. Tho,

your husbands story is just giving me more to worry

about. Hopefully he will find the trick and feel

better soon.

Posts: 34 | From NJ | Registered: Mar 2011  |  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.