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 » Marshall/ Buhner Hybrid Protocol

 - UBBFriend: Email this page to someone!    
Author Topic: Marshall/ Buhner Hybrid Protocol
memphisbluesman
Member
Member # 11570

Icon 1 posted      Profile for memphisbluesman     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am curious if anyone has thought of or experimented with using the Marshall Protocol with herbs instead of Minocycline? I know Dr. K wrote a year or two back that he was hopeful that a non antibiotic version of the MP would emerge.

I always said that I would be the last person to even consider the sun avoidnce required with the MP because I pracrically grew up on water skis and sailboats, but I have noticed that over the last two years I have had an increasingly bad reaction to sunlight.

I got the D-Metabolites test done and my 1-25 D was a whopping 79 with the normal range being 20-60. MY 25-D was only 27 so my ratio was right around 3. According to the MP site this makes my test results about as tell-tale as you can get.

I have gotten to the point to where my GI tract just doesnt tolerate ABX anymore.

[ 11. June 2007, 01:24 AM: Message edited by: memphisbluesman ]

Posts: 26 | From Memphis, TN | Registered: Apr 2007  |  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 
Memphisb,

"I know Klinghardt wrote a year or two back that he was hopeful that a non antibiotic version of the MP would emerge."

Could you point me to that "writing"? In which context?

Dr. K. is not anti-abx in general (I was on short-term abx myself under his direction), and just wondering what he was talking or writing about. I am pretty sure that he thinks MP was disappointing when he tried it with certain people.

Take care.

Posts: 9834 | From Washington State | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 10 posted            Edit/Delete Post   Reply With Quote 
welcome memphis!

please edit your post removing drs. last name, and only show DR. K! it's against rules of this board ok.

here's how to do this:

click on pencil to right side of your name, and that opens up both subject line and body text. now delete his last name after the K pleas.
click edit send when done.


now do a SEARCH, found at top under new post.

type in Marshall Protocol or MP for 2nd try
MEDICAL
TOPIC LINE
ANY DATE....make sure you have EDITED MY PROFILE TO SHOW LONGEST PERIOD OF TIME vs. default.

leave membership no. blank, hit send.

read ALL posts/replies about MP; many of them here. [Wink]

IP: Logged | Report this post to a Moderator
memphisbluesman
Member
Member # 11570

Icon 1 posted      Profile for memphisbluesman     Send New Private Message       Edit/Delete Post   Reply With Quote 
GIGI, I am referencing page 15 of 34 of the essay titled " A Look Beyond Antiobiotics". It is available in its entirety on Scott's website.

"Often patients develop sarcoidosis, which is rarely recognized (11). The
Lyme infected lymph nodes produce abnormal amounts of 1.25 di-hydroxy
vitamin D. The client often develops marked osteoporosis (most often in the
spine) along with other more typical Lyme symptoms. The blood test (1.25
di-OH vit D) will usually reveal the pathology (levels over 45), necessitating
therapy with the "M" protocol (18). It uses antibiotics together
with the angiotensin II receptor blocker olmesartan -medoxomil. By adding
the KMT lymph drainage technology twice/week results are often rapid and
miraculous. We hope to find alternatives to the antibiotic regimen in the near
future."

If Dr. K has a more updated opinion on the MP I would love to hear it. This essay is about 16 months old so I am sure he has treated several patients with the MP since then in order to build a stronger opinion one way or the other.


Betty, sorry about the name bit. I have actually been lurking here for over a year and rarely post. I can assure you that I have read every thread ever written about the MP. I simply am curious if anyone has experimented with an herbal version.

Posts: 26 | From Memphis, TN | Registered: Apr 2007  |  IP: Logged | Report this post to a Moderator
jarjar
LymeNet Contributor
Member # 8847

Icon 1 posted      Profile for jarjar     Send New Private Message       Edit/Delete Post   Reply With Quote 
The MP abx don't bother my stomach as they are low dose pulsed. I have heard others on this board mention that the MP abx don't upset their stomach either.

You only have to take a small dose of zith every 10 days and others every other day at low doses.

I do take Nature Biotics a S.B.O. product to protect my stomach.

With your 1.25 that high believe me you will feel a difference on the protocol.

Posts: 805 | From Utopia | Registered: Feb 2006  |  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.