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 » Do you have to take Flagyl? from LymeMD blog

 - UBBFriend: Email this page to someone!    
Author Topic: Do you have to take Flagyl? from LymeMD blog
janet thomas
Frequent Contributor (1K+ posts)
Member # 7122

Icon 1 posted      Profile for janet thomas     Send New Private Message       Edit/Delete Post   Reply With Quote 
http://lymemd.blogspot.com/2008/07/do-you-have-to-take-flagyl.html

Friday, July 18, 2008

Do You have to take Flagyl?

Flagyl tastes bad and you can't drink alcohol with it: two negative. It causes a significant Herx.

It is thought to only kill Lyme cysts. The alternative drug is Tindamax. Many internet entries claim that Plaquenil also kills Lyme cyst. I have found no substantiation of this claim.

Some patients respond great to Flagyl while others do not. Again, Stratton has found it to be a critical part of his CPN protocol.

One could argue that cysts convert back to the other active forms and that long term therapy against spirochetes and L-forms is adequate. My experience is that Flagyl is helpful.

Spirochetes bathed in Rocephin or Doxycyline have been shown to convert to the cystic form within hours. I don't want to give the Lyme any place to run to. Have meds on board which can kill any of the three forms.

I will reiterate that pulses doesn't make sense to me. This allows for periods of time for the accumulation of large cyst loads. Once daily Flagyl, 250 mg or 500mg is adequate. (Don't tell anyone, but most patients who take low dose Flagyl in the morning seem to be able to drink at night without throwing up).

Cysts show up in the brain tissue of people with brain Lyme. So I can't say it is they are not disease causing. Nobody really knows. I don't use Flagyl in early therapy because patients Herx too much.

It should work as well orally as it does IV. Although there is no evidence based research to support this; many of my worst patients with neuroborreliosis have responded remarkably well when IV Rocephin, Zithromax and Flagly are given.

Another plus of Flagyl is that it treats C. diff. Any patients with a history of C. diff, pseudomembranous colits, are routinely given Flagly to help prevent recurrences of this potentially serious infection.

[ 08-01-2010, 01:26 PM: Message edited by: janet thomas ]

--------------------
I am not a doctor and this is not medical advice but only my personal experience and opinion.

Posts: 2001 | From NJ | Registered: Mar 2005  |  IP: Logged | Report this post to a Moderator
karenl
Frequent Contributor (1K+ posts)
Member # 17753

Icon 1 posted      Profile for karenl     Send New Private Message       Edit/Delete Post   Reply With Quote 
Janet,
my doctor has me on doxy 200 mg and wants me to start today in addition 1,500 flagyl.

I also have cpn.I understand he wants to address the cyst form of lyme. I was on flagyl 750 mg a day without doxy and was not doing too bad.

I think I get started my flagyl on 250 mg and work my way up as I have no time for a mega herx.

But as I understand the flagyl is a must in lyme treatment. I was doing so much better on doxy but probably only because the lyme went in the cyst.

Posts: 1834 | From US | Registered: Oct 2008  |  IP: Logged | Report this post to a Moderator
cleo
LymeNet Contributor
Member # 6646

Icon 1 posted      Profile for cleo     Send New Private Message       Edit/Delete Post   Reply With Quote 
I did not make progress until I gritted my teeth and stuck the flagyl out. First thing to clear was the fog and depersonalization and ear stuff. Then energy got better and the rest is slowly coming along.
Posts: 433 | From new york | Registered: Dec 2004  |  IP: Logged | Report this post to a Moderator
Lymeorsomething
Frequent Contributor (1K+ posts)
Member # 16359

Icon 1 posted      Profile for Lymeorsomething     Send New Private Message       Edit/Delete Post   Reply With Quote 
Cleo, are you pulsing your flagyl or running it daily?

--------------------
"Whatever can go wrong will go wrong."

Posts: 2062 | From CT | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
BackinStOlaf
Frequent Contributor (1K+ posts)
Member # 23725

Icon 1 posted      Profile for BackinStOlaf     Send New Private Message       Edit/Delete Post   Reply With Quote 
Weird that this doc is giving us hints on how we can drink alcohol

--------------------
First Symptom 9/09
Multiple docs, negative Labcorp test
LLMD: 1/10
Positive Igenex/CDC test
Treatment 2/10
2/10-8/10 Amox, ceftin, zith, flagyl
Currently: Bicillin, Minocycline, still dealing with severe breathing issues

 -

Posts: 1121 | From New York, New York | Registered: Dec 2009  |  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.