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 » Herxing alone in Oz - when will the prickling stop?

 - UBBFriend: Email this page to someone!    
Author Topic: Herxing alone in Oz - when will the prickling stop?
littabella
Member
Member # 12976

Icon 1 posted      Profile for littabella     Send New Private Message       Edit/Delete Post   Reply With Quote 
Please help. I have been on IV Rocefin 2g/day for 9 days, started herxing on day 3, prickling skin started day 6.

It starts when the abx goes in & stays until middle of the night. I wake up feeling great. The it starts all again with abx.

Have tried most things suggested on here but no relief. I am ready to stop abx. Does anyone know when the prickling will stop? If it is soon I can make it.

Bella [cussing]

--------------------
Lyme for 7 years. Various low doses oral doxy, amoxil, erythromicin. IV rocephin 2g/day 2 months.

Posts: 24 | From Australia | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
robi
Frequent Contributor (1K+ posts)
Member # 5547

Icon 1 posted      Profile for robi     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sounds like you are herxing. This happens when you are killing of the spirochetes. You may have many different symptoms. Over time they will lessen. It is hard to predict how long. That depends on many factors.

This board is a great place to come for support. We have all been there, done that ........... you will make it through even though it seems like you can't. Hang in there.

robi

--------------------
Now, since I put reality on the back burner, my days are jam-packed and fun-filled. ..........lily tomlin as 'trudy'

Posts: 2503 | From here | Registered: Apr 2004  |  IP: Logged | Report this post to a Moderator
CherylSue
Frequent Contributor (1K+ posts)
Member # 13077

Icon 1 posted      Profile for CherylSue     Send New Private Message       Edit/Delete Post   Reply With Quote 
My LLMD says burning skin is biotoxin die off. You need to detox aggressively. Talk to your doctor about this one.

CherylSue

Posts: 1954 | From Illinois | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
littabella
Member
Member # 12976

Icon 1 posted      Profile for littabella     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thank you Cherylsue and Robi! [kiss] I feel so alone over here. My doctors don't know anything about Lyme disease and are just following what I say.

What is "detox aggressively"? I need to find a doctor I can call in America to help us.

I would not be here today without the support of you fabulous people. Big Hugs.

--------------------
Lyme for 7 years. Various low doses oral doxy, amoxil, erythromicin. IV rocephin 2g/day 2 months.

Posts: 24 | From Australia | Registered: Aug 2007  |  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.