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 » Dr. K's parasite protocol...

 - UBBFriend: Email this page to someone!    
Author Topic: Dr. K's parasite protocol...
17hens
Frequent Contributor (1K+ posts)
Member # 23747

Icon 1 posted      Profile for 17hens     Send New Private Message       Edit/Delete Post   Reply With Quote 
Question about what to expect -

I was on 4 months of Parastroy (before going to Germany for Bionic treatment). I had a very easy time of it, although I'm FULL of parasites.

DD, on the other hand, couldn't handle one week of Parastroy at beginner's dose as it made her stomach acid CRAZY. So we quit, to fight the battle another day.

Just yesterday, I got DD an appt. w/ our old LLMD and told them it was for parasites. He knows nothing about parasites but I'm going in w/ Dr. K's protocol under my arm and begging for help.

Finally, to my question...what could DD expect on the parasite drugs, since they're strong enough to rid in 6 weeks? As in, how bad might it get? Any idea? Nausea, diarrhea, vomiting, fatigue, brain fog??? Oh, no, sounds terrible!!

My concerns are-
1)I haven't done it first so I don't know how she'll feel and
2)if it gets really bad, how will she handle school?

Any input would be much appreciated!

--------------------
"My flesh and my heart may fail, but God is the strength of my heart and my portion forever." Psalms 73:26

bit 4/09, diagnosed 1/10

Posts: 3043 | From PA | Registered: Dec 2009  |  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 
Hens,

My LLMD put me on Alinia for parasites and Babs... I should get that something this week... but I'm scared to try it!

Hopefully someone can help...

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

Posts: 1391 | From Lyme Land | Registered: May 2011  |  IP: Logged | Report this post to a Moderator
sixgoofykids
Moderator
Member # 11141

Icon 1 posted      Profile for sixgoofykids   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Maybe wait for a break. I found parasite treatment to be tough.

Then again, it depends on the parasites. My daughter had no trouble with it at all.

--------------------
sixgoofykids.blogspot.com

Posts: 13449 | From Ohio | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
17hens
Frequent Contributor (1K+ posts)
Member # 23747

Icon 1 posted      Profile for 17hens     Send New Private Message       Edit/Delete Post   Reply With Quote 
Can you describe tough?

--------------------
"My flesh and my heart may fail, but God is the strength of my heart and my portion forever." Psalms 73:26

bit 4/09, diagnosed 1/10

Posts: 3043 | From PA | Registered: Dec 2009  |  IP: Logged | Report this post to a Moderator
Knight33
LymeNet Contributor
Member # 22028

Icon 1 posted      Profile for Knight33     Send New Private Message       Edit/Delete Post   Reply With Quote 
I just started Dr. K's parasite protocol. I'm on ivermectin right now (2nd on the rotation).

Let me tell you... it's rough... my brain fog hasn't been this bad since I first got sick. My doctor told me to keep going though and push through it.

Just make sure you do some detox stuff with it. I'm doing chlorella and coffee enemas. Also about to add detoxamin. The parasites release a lot of biotoxins and metals and such when they are killed.

I was also put on miracle mineral solution (mms) at the same time as the ivermectin so I'm not sure which caused my brain fog to come back so bad. I stopped taking to mms but continued with the protocol.


Oh, and this protocol really does work. Worms are literally pouring out of me. It's sort of dramatic though. I never had any stomach problems or anything either. Crazy.

Posts: 121 | From Houston, TX | Registered: Aug 2009  |  IP: Logged | Report this post to a Moderator
GiGi
Frequent Contributor (5K+ posts)
Member # 259

Icon 1 posted      Profile for GiGi         Edit/Delete Post   Reply With Quote 
Parasite treatment is tough especially if your body cannot regulate toxic metals. Parasites are loaded with them and flood the system at die-off.

I have been warning people to test for KPU -- that crashes are tough if you have it, and even worse if you have become allergic to the metals - If you kill, you have to be prepared with the fallout and know what to do, whether you use pharmaceuticals, green laser, infrared, or literally any mobilizing therapy. Even accupuncture can spread the toxins around. It is not a herxheimer - it is flooding the system with toxins that makes it difficult for organs, especially the kidneys. Do protect yourself --
binders, binders, butyrate, Unda 243, Solidago, charcoal, microsilica, and more....

Knight33, good luck, and do rule out KPU --- it costs very little to find out and the benefits if corrected are huge! If you learn to test yourself, it is very easy to figure out what the body needs next to avoid crises and to feel better.

http://www.klinghardtacademy.com/images/stories/powerpoints/hpu%202009.pdf
http://planetthrive.com/2010/04/hpukpu-protocol-for-lyme-and-autism/

Take care.

Posts: 9834 | From Washington State | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
17hens
Frequent Contributor (1K+ posts)
Member # 23747

Icon 1 posted      Profile for 17hens     Send New Private Message       Edit/Delete Post   Reply With Quote 
Knight, oh my goodness, you said the dreaded brain fog word! That is my biggest fear! She's got school! Ugh!

Thank you, GiGi. I'll look into it too.

--------------------
"My flesh and my heart may fail, but God is the strength of my heart and my portion forever." Psalms 73:26

bit 4/09, diagnosed 1/10

Posts: 3043 | From PA | Registered: Dec 2009  |  IP: Logged | Report this post to a Moderator
phil C
Member
Member # 34473

Icon 1 posted      Profile for phil C     Send New Private Message       Edit/Delete Post   Reply With Quote 
is there a definitive way to test for parasites

--------------------
my wife and I and all 4 of our children have chronic lyme disease. My mission is to fix that.

Posts: 30 | From NJ | Registered: Oct 2011  |  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 
hens, the brain fog is more the mms than the parasite treatment...
Posts: 1834 | From US | Registered: Oct 2008  |  IP: Logged | Report this post to a Moderator
canefan17
Frequent Contributor (5K+ posts)
Member # 22149

Icon 1 posted      Profile for canefan17     Send New Private Message       Edit/Delete Post   Reply With Quote 
phil c,

By treating

The stool tests are less accurate than Lyme tests.

[ 11-02-2011, 10:24 PM: Message edited by: canefan17 ]

Posts: 5394 | From Houston, Tx | Registered: Aug 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.