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  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Seeking a Doctor » Need a doctor in Upstate NY who uses the rife machine for treatment

 - UBBFriend: Email this page to someone!    
Author Topic: Need a doctor in Upstate NY who uses the rife machine for treatment
butterfly23
Junior Member
Member # 44719

Icon 1 posted      Profile for butterfly23     Send New Private Message       Edit/Delete Post   Reply With Quote 
Does anyone know of a doctor in upstate new York who diagnoses lyme disease with an electrodermal machine (also called a body scan) and treats lyme disease with a rife machine + supplements?
Posts: 1 | From Syracuse, New York | Registered: Sep 2014  |  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 
-
Rife is deemed "experimental" and therefore MDs are not allowed by law to do more than answer a question about rife if YOU bring it up. They are not allowed to use a rife machine for patients or even suggest it. NDs are, though.

IF you bring it up first, MDs can share what other patients may have told them of their experiences with rife, though that's where their freedom to talk about it stops.

As for diagnostics with an electrodermal machine, indeed, it can be very helpful but you want far more than that, too. And for the coinfections as well.

You need the wisdom of a very experienced ILADS educated LL doctor to clinically assess you, taking into account their experience, their training, your history and your current presentations / symptoms / abilities.

Such assessment will be important not just to determine if you "have" it but also what body systems / organs might be most affected . . . and what kinds of treatments might best work.

And . . . what coinfections might be involved.

A clinical assessment is really important. A LLMD can certainly assess you. Just explain you are not so interested in the CDC tests or others if they are out of your reach or need to save money for actual treatments that might be within reach.

For other methods, in addition, So you might look for a LL ND. LLMDs may know of some, too.

Hope you get some specific replies, of course. Ultimately, it's more cost effective to get your own rife . . . still, it's great to have a LL ND guide you. Good luck.


http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=117755;p=0

Topic: RIFE Machine - Reference LINKS & How to Find an ILADS educated LL ND
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  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 
-
I'm likely going out on a huge limb here, too. But I'm so tired of so many not having money for treatments.

If you have only so much, and if that might cover getting a rife machine but no more . . . I would get the rife and do your very intelligent best to go forward from there.

It's not ideal but we have to do a priority list. It will serve no purpose to assess if you won't have means to treat. So my advice above might just be turned on its head.

IMO, the top priority is being able to have a rife machine of your own if this is the path you choose.

Of course, it's best to have expert medical assessment so you know as well as you can what you are dealing with - and expert guidance and do your best to attain that but, if it's just not possible, certain choices might need to be made in light of practical matters. Good luck.
-

[ 09-29-2014, 08:20 PM: Message edited by: Keebler ]

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
hopingandpraying
Frequent Contributor (5K+ posts)
Member # 9256

Icon 1 posted      Profile for hopingandpraying     Send New Private Message       Edit/Delete Post   Reply With Quote 
Check the online state Lyme groups at:
http://health.groups.yahoo.com/group/newyorklyme

Maybe they can help.

Some more resources for you (including Support Groups info):
www.lyme-aware.org/new-york.html
www.empirestatelymediseaseassociation.org

Posts: 8981 | From Illinois | Registered: May 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  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.