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 » Anyone use chitopower to help herxing?

 - UBBFriend: Email this page to someone!    
Author Topic: Anyone use chitopower to help herxing?
valymemom
Frequent Contributor (1K+ posts)
Member # 7076

Icon 1 posted      Profile for valymemom     Send New Private Message       Edit/Delete Post   Reply With Quote 
This morning I read the information explaining herxing posted by TheSkyKing and saw chitopower mentioned to help with a herx.

Who has found it beneficial?


Posts: 1240 | From Centreville,VA | Registered: Mar 2005  |  IP: Logged | Report this post to a Moderator
minoucat
Frequent Contributor (1K+ posts)
Member # 5175

Icon 1 posted      Profile for minoucat     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi there. I did not use chitopower, but I did use CSM, which I think is functionally similar (binds toxins). I don't know -- I couldn't pull up the webpage.

I think CSM may have helped over the long run to bind neurotoxins--or something-- and get rid of them; but it made my headache much worse at the start of using it (by my 3rd time using it, no headache. But a lot of other things had changed by then, too).

I don't know what to think about the whole Bb/babs neurotoxin theory -- I've read arguments pro and con, and my own experience is not definitive.

Mostly I'm just responding to bounce this back up the page and get more input. I hope your son finds relief soon (for your sake, too. It's terrible to watch the people you love suffer). If you need more herx relief ideas, let us know.


Posts: 2331 | From WA | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
Kira
LymeNet Contributor
Member # 2676

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

I've used ChitoPower and it did help me a lot...The only thing is that it is so very expensive...~$100 a bottle...so it's hard to be able to afford it on an ongoing basis.

During my worst herxes I was popping 6 capsules several times a day...so the bottle would be gone in a week or two...but it worked where other stuff that I knew of wasn't at the time. Helped clear my brain fog and achiness.

It's better than plain Chitosan because it has smaller molecules and can bind to toxins even in the blood stream, vs just like fibre (Chitosan) in the gut.

Now that I have experienced how beneficial coffee enemas are, though...I would consider giving that a try first (less expensive), but if I could afford Chito power on an ongoing basis, I would certainly continue to use it!!

All my best,
Kira


Posts: 802 | From Chicago suburbs, Illinois | Registered: Jun 2002  |  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.