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 take Lymphomyosot?

 - UBBFriend: Email this page to someone!    
Author Topic: Anyone take Lymphomyosot?
Love my kids
LymeNet Contributor
Member # 32876

Icon 1 posted      Profile for Love my kids     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi,

I take Lymphomyosot, liquid vials. Anyone else? I used to find it online for about $50 for 10 vials. Now, can't find it for under $100. I do this every other day Sub Q so that is pricey! It does help with detox for me so I'd like to continue.

Thanks for any leads.

--------------------
Healing thoughts to you,

L.

Posts: 101 | From USA | Registered: Jul 2011  |  IP: Logged | Report this post to a Moderator
feelfit
Frequent Contributor (1K+ posts)
Member # 12770

Icon 1 posted      Profile for feelfit     Send New Private Message       Edit/Delete Post   Reply With Quote 
I did about 5 treatments of Lymphomyosot IV and it helped immensely with detox/lymph buildup. My doctor had me continue on Lymphomyosot drops, not vials.

I have done 15 drops 2x day since Jan. and my puffiness/swelling has not returned. HAve you considered/tried the drops? They can be taken orally or rubbed on the skin.

Best!

Posts: 3975 | From usa | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
Energy2Heal
LymeNet Contributor
Member # 2010

Icon 1 posted      Profile for Energy2Heal     Send New Private Message       Edit/Delete Post   Reply With Quote 
You can buy Lymphomyosot drops online at www.iherb.com. Much less expensive - only about $23 per bottle. I take 10 drops 3x per day.

They also have tablets there even cheaper. I prefer the drops, but tabs could come in handy if you have to be on the go.

Posts: 443 | From The Wild West | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
chootik
LymeNet Contributor
Member # 11221

Icon 1 posted      Profile for chootik     Send New Private Message       Edit/Delete Post   Reply With Quote 
I got the liquid vials from my doc and he wanted me to do injections but on the bottle it said for consumption by mouth only so I didn't do the injections.

I'm wondering did you guys buy the ones that are for injection or are using the oral liquid for injection?

Thanks

Posts: 247 | From Ca | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
Energy2Heal
LymeNet Contributor
Member # 2010

Icon 1 posted      Profile for Energy2Heal     Send New Private Message       Edit/Delete Post   Reply With Quote 
There are four kinds of Lymphomyosot - tablets, oral drops, oral vials and IV vials.

The first three are available on iHerb.

I have used all four, although I don't know where to get the IV vials in this country (haven't looked for them here)

You should never use the oral drops or oral vials for injections. I am currently using the oral drops.

Posts: 443 | From The Wild West | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
chootik
LymeNet Contributor
Member # 11221

Icon 1 posted      Profile for chootik     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks Andrew.

That's what I thought! But the doc said he has others using the oral vials for injections, which I thought was kinda crazy.

I think the IV vials you would have to get from Germany. At the time the doc was out of the IV vials but I'm not sure if we can get it without a perscription.

Posts: 247 | From Ca | Registered: Feb 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 
When you can feel the little balls under your chin, it is time for Lymphomyosot - any form. I also use Poke Root drops and Red Rood drops.

When the lymph is stuck, toxins can't get out and nutrients cannot get in.

Posts: 9834 | From Washington State | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
mlg
LymeNet Contributor
Member # 35383

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

Have you tried Itires?

Posts: 697 | From CA | Registered: Dec 2011  |  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.