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 » Artemisinin Question?

 - UBBFriend: Email this page to someone!    
Author Topic: Artemisinin Question?
lymebytes
Frequent Contributor (1K+ posts)
Member # 11830

Icon 1 posted      Profile for lymebytes   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi - have any of you taken artemisinin for Babesia?

I am trying to remember what dose I took (for only a month) way back and I believe the dose was 200mg 2x's per day - does this sound right?

And what vitamin cannot be taken with it? Is it COQ10? Any other? Also, should it be pulsed?

Lastly - anyone with real progress using it?

Thanks!

[ 10. October 2007, 08:28 PM: Message edited by: lymebytes ]

--------------------
www.truthaboutlymedisease.com

Posts: 2003 | From endemic area | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
SForsgren
Frequent Contributor (1K+ posts)
Member # 7686

Icon 1 posted      Profile for SForsgren         Edit/Delete Post   Reply With Quote 
I have used up to 1500mg for 3 days per Dr. K recommendations. It did not work. I still have Babesia. Of all the alternative therapies, Artemisinin is one that I have not found useful - though others have.

CoQ10 and I have heard some suggest Milk Thistle both be avoided.

--------------------
Be well,
Scott

Posts: 4617 | From San Jose, CA | Registered: Jul 2005  |  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 
Not sure what other LLMDs protocol is. Dr. Z protocol artemesinin protocol is 40 days, perhaps 80, but not at the dose referred to above by Dr. K

I'm curious why just 3 days? Scott, can you elaborate ?

And are CoQ10 and Milk Thistle avoided all together with artem. or just at the same dose time for a few hours ?

I'm assuming that they make take the medicine back out of body too fast for the reason why?

-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
winelyme
Member
Member # 11897

Icon 1 posted      Profile for winelyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi,

I have taken �rt twice and it seems to be helping. �t first I took
200mg 2x a day. Now I'm pulsing 400mg 3x a day for 3 days, off
for 3 weeks. Yes, you don't want to take COQ10 with �RT.

Good Luck [Smile]

Posts: 30 | From northern california | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
cbb
Frequent Contributor (1K+ posts)
Member # 788

Icon 1 posted      Profile for cbb     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've read that CoQ10 should not be taken with Mepron or Malarone.
What is the problem with taking it with Artemisinin?

Posts: 4638 | From South Carolina | Registered: Mar 2001  |  IP: Logged | Report this post to a Moderator
steven
LymeNet Contributor
Member # 13101

Icon 1 posted      Profile for steven     Send New Private Message       Edit/Delete Post   Reply With Quote 
just started artemisinin (200 mg/day) a few days go - im also still on biaxin and malarone (2 tbl./day).

cant say that malarone or arte has changed much - at least so far. maybe no babesia?

Posts: 226 | From earth | Registered: Sep 2007  |  IP: Logged | Report this post to a Moderator
bejoy
Frequent Contributor (1K+ posts)
Member # 11129

Icon 1 posted      Profile for bejoy     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have been taking Artemicin (or some form of Wormwood) for about a year, with occasional breaks of weeks or a month.

I make most of my decisions about what to take and how long based on muscle testing.

Artemicin keeps coming up positive and necessary for me month after month.

Note that the bottle says not to take for more than three weeks, so I'm not making recomendations to take it longer, even though it seems to be working well for me.

I can't say exactly how much it has helped me, since I take it concurrently with several other things, but my health is continuing to improve.

One thing I have noticed is that Artemicin healed sores in my nose that I have had for many years and couldn't seem to get rid of.

I know it was a result of Artemisin because the sores came back when I discontinued, and went away when I started back up.

I had always thought the sores were candida related, but now based on some posts about people possibly getting nosebleeds from babs,

I am wondering if they might have been from Babesia.

--------------------
bejoy!

"Do not go where the path may lead; go instead where there is no path and leave a trail." -Ralph Waldo Emerson

Posts: 1918 | From Alive and Well! | Registered: Feb 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.