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 » About to start flagyl.. any advice?

 - UBBFriend: Email this page to someone!    
Author Topic: About to start flagyl.. any advice?
DDEC2
Member
Member # 30313

Icon 1 posted      Profile for DDEC2     Send New Private Message       Edit/Delete Post   Reply With Quote 
Currently in my 4th month of treatment. I am currently on Azith and Ceftin.

My LLMD decided its time to add flagyl to the mix. Ive read the horror stories on here and was just wondering what can i expect and what precautions should i take?

Thanks.

--------------------
Igenex results 4-6-2011:
IGM 23-25:IND,31++,41++,58+,66+,83-93+

IGG 30+,39+,41+++

Posts: 80 | From Chicago IL | Registered: Jan 2011  |  IP: Logged | Report this post to a Moderator
Parisa
LymeNet Contributor
Member # 10526

Icon 1 posted      Profile for Parisa     Send New Private Message       Edit/Delete Post   Reply With Quote 
Some people have a hard time with it and others don't. My husband made great progress on Flagyl. The type of improvement where you improve daily.

Good luck!

Posts: 984 | From San Diego | Registered: Nov 2006  |  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 
I'm taking IV Flagyl and did fine last month. I only pulse it for one week per month... so so far so good. Nothing bad to report here and too early to tell if it's helping!

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

Posts: 1391 | From Lyme Land | Registered: May 2011  |  IP: Logged | Report this post to a Moderator
LBS
LymeNet Contributor
Member # 33323

Icon 1 posted      Profile for LBS     Send New Private Message       Edit/Delete Post   Reply With Quote 
DDEC2 - I started Flagyl today, sliver of a pill. How is it working for you?

--------------------
Tick Bite: March 2011
ABX Treatment: August 2011
Diagnosed: September 2011

Posts: 137 | From God's Got This! | Registered: Aug 2011  |  IP: Logged | Report this post to a Moderator
TF
Frequent Contributor (5K+ posts)
Member # 14183

Icon 1 posted      Profile for TF     Send New Private Message       Edit/Delete Post   Reply With Quote 
My advice is to adhere strictly to the anti-yeast diet while on flagyl so as to avoid getting a yeast infection.

From page 15 of Burrascano; all the flagyl tips:

"Important precautions:

1. Pregnancy while on Flagyl is not advised, as there is a risk of birth defects.

2. No alcohol consumption! A severe, "Antabuse" reaction will occur, consisting of severe nausea,
flushing, headache, and other symptoms.

3. Yeast overgrowth is especially common. A strict anti-yeast regimen must be followed.

4. Flagyl can be irritative to the nervous system- in the short term, it may cause irritability, "spacey" feelings, etc. Longer term, it can affect the peripheral nerves, causing tingles, numbness, etc. If mild, a change in dose may be required. Often, extra vitamin B can clear these symptoms. If the nerve
symptoms persist or are strong, then metronidazole must be discontinued or these symptoms may become very long lasting.

5. Strong Herxheimer-like reactions are seen in almost everyone."

http://www.ilads.org/lyme_disease/B_guidelines_12_17_08.pdf

Posts: 9931 | From Maryland | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
Kramberry
LymeNet Contributor
Member # 34032

Icon 1 posted      Profile for Kramberry     Send New Private Message       Edit/Delete Post   Reply With Quote 
Are you addresing any co infections?

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

Posts: 215 | From California | Registered: Sep 2011  |  IP: Logged | Report this post to a Moderator
Kudzuslipper
Frequent Contributor (1K+ posts)
Member # 31915

Icon 1 posted      Profile for Kudzuslipper     Send New Private Message       Edit/Delete Post   Reply With Quote 
years ago, before a Lyme DX, i took flagyl and cipro for diverticulitis. I remember my reaction, because my doctor who had been out of town when I went in called me to see how i was doing, and I remember telling her "I was fantastic, in fact giddy, and have a ton of energy and nothing hurts" we both assumed that it was just because my gut had made me feel so bad... now of course I wonder if it was because of Lyme. And of course I don't remember how I felt later in the course.

Although not sure how I would react now that I have been on different abx for 5 months and it won't be a 10 day course.

I would say just proceed with caution... if anything bothers you, call your doctor, if your doctor doesn't get back right away and you are nervous just stop it. Or if you are really nervous go to the emergency room of course.

good luck.

Posts: 1728 | From USA | Registered: May 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.