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 » Clove Bud Oil for Bart -- Anyone?

 - UBBFriend: Email this page to someone!    
Author Topic: Clove Bud Oil for Bart -- Anyone?
LymeMECFSMCS
LymeNet Contributor
Member # 13573

Icon 1 posted      Profile for LymeMECFSMCS   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I just ordered some clove bud oil to try for bartonella, following the suggestion of Dr. JS's new book on bart. I'm already taking Rifampin and houttuynia, as well as Cumanda (sometimes) for bart.

I'm not sure how to use the clove bud oil exactly, or what to expect, so I'd love to hear experiences from any who have tried it.

Posts: 929 | From Massachusetts | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
GenaD
LymeNet Contributor
Member # 11988

Icon 1 posted      Profile for GenaD     Send New Private Message       Edit/Delete Post   Reply With Quote 
I got something called "clovanol" and I mix it with olive oil and put it on toast. I was told to work up from 30 to 120 drops of clovanol,and keep the ratio of olive oil to clovanol 3:1. I find it really rather disgusting, but I'm giving it a shot!

So far I really don't feel any herx or side effects but I've only been using cumanda and clovanol about a week.

--------------------
"Never underestimate the power of a few committed people to change the world. Indeed it is the only thing that ever has."
--Margaret Mead

Posts: 290 | From New York | Registered: May 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 
-

Essential oils can be very powerful.

Not all essential oils are for consumption, though, so be sure.

Some essential oils can burn. Be sure to get expert instruction.

some are just meant to be smelled . . . some mixed with a carrier oil, such as almond oil, and rubbed into the skin. Do not go over the number of drops suggested - and be sure the ratio to carrier oil is perfect - otherwise it can burn.

Thieves' is one that is suggested (topically and to smell) for lyme, BTW, based upon a formula used during the plague in Europe. Historically, it has good accounts.

-

[ 06. July 2008, 11:38 PM: Message edited by: Keebler ]

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Alv
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
I have not triede it yet..
i am up to 10 hh capsules...tomorrow will increae in 15

but bart still there....I am planing on adding it...but not for at least 1 month

IP: Logged | Report this post to a Moderator
jamescase20
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
I tried black pepper with levaquine and it took down the "Bart headache" that levaquine seems to make for me.
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.