LymeNet Flash: where can you get rife?

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

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.

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 » Questions and Discussion » Medical Questions » where can you get rife?

UBBFriend: Email this page to someone!

Author

Topic: where can you get rife?

randibear
Honored Contributor (10K+ posts)
Member # 11290

posted

if you cannot afford a rife machine or don't know how to make one, can you go to a doctor or somekind of homeo and get treatments?

do people share a machine or what?

i'd like to try it but can't afford it.

--------------------
do not look back when the only course is forward

Posts: 12262 | From texas | Registered: Mar 2007 | IP: Logged |

psr1
LymeNet Contributor
Member # 22957

posted

I'm with you! Looking for someone in the metropolitan NYC area to share one with.

Posts: 360 | From New York | Registered: Oct 2009 | IP: Logged |

Keebler
Honored Contributor (25K+ posts)
Member # 12673

posted

-
PM with any personal contacts or individual names, do not post on open forum. Links to business are okay to post, though.
--------------------

psr1 - contact your local support groups and all the LLMDs around you - give them a little flyer to pass along if this comes up in conversation with others.

Randi, I just sent you a PM with the contact for a EMEM5a Rife. He makes no profit at all and is extremely nice and honest. I have one of these. For me, the fan is very loud but he's never had anyone else say that.

Have you read Rosner's Rife book yet? It has some very good details.
============

RIFE

http://www.lymebook.com/lyme-disease-rife-machines-bryan-rosner

Book: Lyme Disease and Rife Machines by Bryan Rosner

-

Posts: 48021 | From Tree House | Registered: Jul 2007 | IP: Logged |

jamieL
LymeNet Contributor
Member # 16563

posted

Randi,

I live close to you. Sort of. I'll send you a p.m..

--------------------
Diagnosed with :yme and mycoplasma pneumonia Aug 08.
Treating with Doxy and Ceftin ever since. 15 sessions in hyperbaric o2 chamber

Posts: 183 | From all around | Registered: Jul 2008 | IP: Logged |

Pinelady
Frequent Contributor (5K+ posts)
Member # 18524

posted

Probably no where pretty soon.

http://flash.lymenet.org/ubb/ultimatebb.php/topic/3/24051

They are hitting all our possible treatments. This is so sad. He is 69 years old and they are doing this to him.

~ Rife Researcher Facing 51 Months in Federal Pen!
The Dr. Rima Reports Talks with This Researcher. Listen Now:

http://www.thefreedomlink.org/Dr_Rima_Reports.php
scroll down to "The Dr. Rima Reports with Jim Folsom"

[ 02-22-2010, 05:18 PM: Message edited by: Pinelady ]

--------------------
Suspected Lyme 07 Test neg One band migrating in IgG region
unable to identify.Igenex Jan.09IFA titer 1:40 IND
IgM neg pos
31 +++ 34 IND 39 IND 41 IND 83-93 +
DX:Neuroborreliosis

Posts: 5850 | From Kentucky | Registered: Dec 2008 | IP: Logged |

springshowers
Frequent Contributor (1K+ posts)
Member # 19863

posted

I just posted a link to where they are selling and buying used Rife machines and maybe on that forum you might want to post where you are and your interest.

The link is in the last post of the Rife Thread.. I posted it just today.

Posts: 2747 | From Unites States Of America | Registered: Apr 2009 | IP: Logged |

map1131
Frequent Contributor (5K+ posts)
Member # 2022

posted

I would never risk my machine by using to medically treat another person. Never.
That might sound hard, but that's fact.

Pam

--------------------
"Never, never, never, never, never give up" Winston Churchill

Posts: 6495 | From Louisville, Ky | Registered: Jan 2002 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

You can afford a cruise, but not a $460 rife machine???

They are very cost effective. Just think about it.

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

Posts: 96239 | From Texas | Registered: Feb 2001 | IP: Logged |

lymielauren28
Frequent Contributor (1K+ posts)
Member # 13742

posted

I would in a heart beat, but that's just me. I DARE someone to come try and take my machine away. It would be their last mistake.

--------------------
"The only way out is through"

Posts: 1434 | From mississippi | Registered: Nov 2007 | IP: Logged |

Printer-friendly view of this topic

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
http://www.lymenet.org/