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 » MMS and who has tried it

 - UBBFriend: Email this page to someone!    
Author Topic: MMS and who has tried it
lymewreck36
Frequent Contributor (1K+ posts)
Member # 4395

Icon 1 posted      Profile for lymewreck36     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi guys. I just ran across this on the net. I will do a search for it here on LN. Has anyone here tried this MMS and had good results? If so, where did you buy your product?

Mary

http://mms-articles.com/MMS-intro.htm

Posts: 1032 | From North Carolina | Registered: Aug 2003  |  IP: Logged | Report this post to a Moderator
catskillmamala
LymeNet Contributor
Member # 12536

Icon 1 posted      Profile for catskillmamala     Send New Private Message       Edit/Delete Post   Reply With Quote 
MMS almost killed me. I got to 8 drops a day and had to be hospitalized for thrombocytopenia- a severe drop in platelets (<7,000 when it should be over 140,000).

I was at risk for internal bleeding. Blood vessels were breaking all over my body. I had to quit all other lyme meds and protocols and go on steriods for 3 months.

Not good for me! Just have to give my 2 cents.

Posts: 524 | From Hudson Valley, NY | 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 
Couldn't take it. Gave me terrible heartburn.

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

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
kitty9309
LymeNet Contributor
Member # 19945

Icon 1 posted      Profile for kitty9309     Send New Private Message       Edit/Delete Post   Reply With Quote 
Dangerous stuff. Not meant to be ingested. It is a disinfectant.

http://www.osha.gov/SLTC/healthguidelines/chlorinedioxide/recognition.html

Posts: 819 | From East Coast | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
steelbone
LymeNet Contributor
Member # 14014

Icon 1 posted      Profile for steelbone     Send New Private Message       Edit/Delete Post   Reply With Quote 
Some people do it transdermally.

I did it transdermally a few times.

Guess you could say i was a bit chicken with this stuff knowing how powerfull it can be.

Still there seems to be some people that do really well with it.

--------------------
All The Best,
Paul
[email protected]

The harder you work the luckier you get!

Posts: 965 | From Nebraska Cornhuskers fan in Massachusetts | Registered: Dec 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.