LymeNet Flash: What is a rife machine?

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 » What is a rife machine?

UBBFriend: Email this page to someone!

Author

Topic: What is a rife machine?

Nal
Frequent Contributor (1K+ posts)
Member # 6801

posted

Ive heard mention on it here but Im wondering what it is and how it works. Is it expensive?

Nancy

Posts: 1594 | From Colorado | Registered: Jan 2005 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

Why don't you do a search on Google? I really can't explain it. Basically it uses frequencies to zap the spirochetes. A man named Royal Rife invented it in the 1930's.

About the same time, penicillin was discovered. And of course, the medical establishment ignored the Rife for the most part.

You can get a "no-rift" rife for around $75. The next cheapest is around $450. Mine should be arriving in about 2 wks! Yippeeee!!

You really should order skyking's book. You'll learn alot about Lyme. [and rife]
www.lymebook.com

------------------
oops!
Lymetutu

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

janet thomas
Frequent Contributor (1K+ posts)
Member # 7122

posted

I second that endorsement of the book, very informative. Many years of Lyme knowledge.

Posts: 2001 | From NJ | Registered: Mar 2005 | IP: Logged |

ivebeentricked
Member
Member # 6944

posted

I am so sick of abx and I know how bad they are for us, but I have also heard some very scary things about rife machines. I have corresponded with w number of people who say they have done more harm than good and one woman claims that it really screwed up her nervous system.

who has used them with success? is there anyone with any problems from them?

Posts: 99 | From California | Registered: Feb 2005 | 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/