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 Protocol

 - UBBFriend: Email this page to someone!    
Author Topic: Marshall Protocol
Ellen101
Frequent Contributor (1K+ posts)
Member # 35432

Icon 1 posted      Profile for Ellen101     Send New Private Message       Edit/Delete Post   Reply With Quote 
I was wondering who here has done or are doing the Marshall Protocol. If you are doing it now are you noticing improvement compared to what you were seeing with traditional lyme treatment?

I'm really confused as to which way to go. My Vit D was extremely low so my PCP had me take a high dose once a week for 3 months to bring it back up and now I'm taking 1000mg /day. I see that Vit D is contraindicated in the protocol.

Posts: 1748 | From United States | Registered: Dec 2011  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Personally, I would pass.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
JRWagner
Frequent Contributor (1K+ posts)
Member # 3229

Icon 1 posted      Profile for JRWagner     Send New Private Message       Edit/Delete Post   Reply With Quote 
1. Protocol is dangerous/unhealthy... Vit. D3 is essential for optimization of immune system, etc.
2. Marshall lists a RESEARCH FOUNDATION... turns out to be his HOME ADDRESS.
3. Marshall lists a hospital affiliation... HIS WIFE WORKS THERE... NOT HIM!
Ego maniac... bogus treatment.

Pass...

Posts: 1414 | From Ny, Ny | Registered: Oct 2002  |  IP: Logged | Report this post to a Moderator
Neil M Martin
LymeNet Contributor
Member # 2357

Icon 1 posted      Profile for Neil M Martin     Send New Private Message       Edit/Delete Post   Reply With Quote 
The "protocol" seemed worth a try as my Vitamin D levels were out of range high. It was a very detailed protocol but an MD and ND suggested that I consider it.

After over a year on Benicar I had better stamina and mental clarity but my BP was 80/40. I felt more ligh headed than normal and weak, and discontinued Benicar went back to my prior routine on oral antibiotics alone.

Then my ankles and feet began to swell. My GFR
was low (is now back to normal) and my doctor said I was not supposed to up and quit Benicar.

I now take water pills for my kidneys.

I called MP. Dr. Marshall answered. He said you need ongoing advice from the MP web site: it is virtually impossible to succeed with on protocol on your own.

Sounding a bit gruff, he directed me to his web site. I do not think he was that interested in my situation.

This is only my experience. The protocol may have helped others. I still avoid sunlight and reduce my Vitamin D intake.

--------------------
Neil

Posts: 697 | From Tucson, AZ USA | Registered: Apr 2002  |  IP: Logged | Report this post to a Moderator
Ellen101
Frequent Contributor (1K+ posts)
Member # 35432

Icon 1 posted      Profile for Ellen101     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for all the feedback. After alot of reading and reviewing what was posted I really don't think it is for me.

To begin with my Vit D was extremely low where as it seems those who went that route had high levels to begin with.

Posts: 1748 | From United States | Registered: Dec 2011  |  IP: Logged | Report this post to a Moderator
CD57
Frequent Contributor (1K+ posts)
Member # 11749

Icon 1 posted      Profile for CD57     Send New Private Message       Edit/Delete Post   Reply With Quote 
You will not find much support for MP on here, Ellen. I know several who went through high dose abx and did not improve, only to recover their health on MP. It's same as anything, works for some and not others.
Which of your Vit D's was low? You need to get two measurements, 1,25 D and 25-OH. One is usually low and the other high in Lyme and chronically ill people.

Posts: 3528 | From US | Registered: Apr 2007  |  IP: Logged | Report this post to a Moderator
CD57
Frequent Contributor (1K+ posts)
Member # 11749

Icon 1 posted      Profile for CD57     Send New Private Message       Edit/Delete Post   Reply With Quote 
By the way, as the far as the danger of the protocol....what we are doing here with high dose long term antiobiotics is pretty dangerous....but we and our doctors seem to blow that right off.
Posts: 3528 | From US | Registered: Apr 2007  |  IP: Logged | Report this post to a Moderator
Ellen101
Frequent Contributor (1K+ posts)
Member # 35432

Icon 1 posted      Profile for Ellen101     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks CD 57 I will have to pull out my labs and check them out.

Yes, you have a really good point what we are doing here with antibiotics, parasite treatments etc is definitely very dangerous as well.

Posts: 1748 | From United States | Registered: Dec 2011  |  IP: Logged | Report this post to a Moderator
lymewarrior03
LymeNet Contributor
Member # 3891

Icon 1 posted      Profile for lymewarrior03   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
M.P. is a hoax that preys on desperate sick people
Posts: 661 | From NY | Registered: May 2003  |  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 
-
You are NOT a candidate for the MP, with your vitamin levels. It's just that simple. You would not qualify.

It's for those with HIGH Vitamin D but even then, IMO, after much study, I think it is far too limited for anyone with any tick-borne infection and can be quite dangerous.
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
(old thread)

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
Ellen101
Frequent Contributor (1K+ posts)
Member # 35432

Icon 1 posted      Profile for Ellen101     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by Lymetoo:
(old thread)

Yes, this was back in December, but thanks for the responses
Posts: 1748 | From United States | Registered: Dec 2011  |  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 
-
Ohhhhh . . . I dive right in and forget to look at the date.

Thanks for waking up my brain and reminding me to FIRST look at the posting date. It can sure save time when we check the date.
-

Posts: 48021 | From Tree House | Registered: Jul 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.