LymeNet Flash: Can't recover from last Rife treatment-please help

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 » Can't recover from last Rife treatment-please help

UBBFriend: Email this page to someone!

Author

Topic: Can't recover from last Rife treatment-please help

Mariel25
Member
Member # 45205

posted

Did Rife almost two weeks ago and can't recover. Thought processes are totally messed up and I am up all night until 6:00 am when I sleep for about three hours. How can I get out of this? Hadn't Rifed for over two years and did 2 minutes on 10 frequencies. To make matter worse, my doctor's office is not calling me back after I was supposed to be on treatment a month ago. Your thoughts are apprecaited.

Posts: 61 | From Connecticut | Registered: Jan 2015 | IP: Logged |

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

posted

-
While seemingly very conservative, a total of 20 minutes the first time (back) may have been a bit too long for your body. Or maybe using 10 different frequencies the first time back out of the gate was too much.

Did you end with 10K? You can do 10K every day

(even though you followed the guideline that "rifing for lyme should be no less than 12 days apart" . . . or until a herx is cleared).

Ending each session with 10K and using it daily can really help calm inflammation and the herx response.

Still, if you did that (or do in the future) it may not be enough. Maybe your liver support needs some adjusting.

So sorry to hear of your reaction. I have to think there is something that will help. And that you can get back to rife, too, when this clears up a bit.
-

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

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

posted

-
I suggest calling a LL ND (naturopathic doctor) who would also be rife "literate" at least to some degree.

MDs are not allowed to discuss rife or guide treatment with rife specifics, other than to share brief comments that others may have shared with them about their experiences. A LLMD would be able to guide the support around rife, however.

Your local lyme support groups would be the place to start asking about any LL NDs who know about rife.

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=123746;p=0

Topic: MAGNESIUM - Informational Links set

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=3;t=030792;p=0

LIVER & KIDNEY SUPPORT & and several HERXHEIMER support links, too.
-

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

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

posted

-
You might want to post this question over in the discussion thread, too:

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

Topic: RIFE Machine - Reference LINKS
-

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

Mariel25
Member
Member # 45205

posted

Thanks- this is awful. You try to do something you think can help and you end up in worse shape.

Posts: 61 | From Connecticut | Registered: Jan 2015 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

Sure hope you can get back to square one. Do anything you can to detox.

[group hug]

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

Posts: 96222 | From Texas | Registered: Feb 2001 | IP: Logged |

Mariel25
Member
Member # 45205

posted

Thank you- I'll try to detox. Not much else to do but wait it out.

Posts: 61 | From Connecticut | Registered: Jan 2015 | IP: Logged |

hopingandpraying
Frequent Contributor (5K+ posts)
Member # 9256

posted

Here is the link for the "Rife Support and Sharing Thread":

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=088778;p=0

Check the online state Lyme groups at:
https://groups.yahoo.com/neo/groups/ConnecticutLyme/info

Maybe they can help.

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

http://www.lymenet.org/SupportGroups/UnitedStates/Connecticut/

Posts: 8981 | From Illinois | Registered: May 2006 | 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/