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 » Who hasn't rife helped? (Page 3)

 - UBBFriend: Email this page to someone!   This topic comprises 3 pages: 1  2  3   
Author Topic: Who hasn't rife helped?
D Bergy
Frequent Contributor (1K+ posts)
Member # 9984

Icon 1 posted      Profile for D Bergy     Send New Private Message       Edit/Delete Post   Reply With Quote 
It has always been a mystery how it can work for one person and not another.

I understand that happening with, for instance, my Crohn's treatment of using LDN. It is known to work about 70 to 80% of the time. Since it is altering the immune response, I can understand that is going to vary for each individual.

Frequency treatment for Lyme should kill Spirochetes, at the very least, in anyone. I noticed some do get a Herx, but do not improve otherwise. That makes some sense, as this can happen using any treatment.

I am not sure if it is a detox issue or what it is, but that problem is not so much a treatment problem, but something else. If four different treatment methods produce the same result, then you have to find out the reason for lack of recovery other than the method of killing Lyme. Certainly one of four methods should have produced some improvement.

What really puzzles me is no reaction at all, good or bad. That one I have no explanation for.
I wish I knew the answer, because not knowing does not help anyone.

Dan

Posts: 2924 | From Minnesota | Registered: Aug 2006  |  IP: Logged | Report this post to a Moderator
Porsche
LymeNet Contributor
Member # 7644

Icon 1 posted      Profile for Porsche     Send New Private Message       Edit/Delete Post   Reply With Quote 
Lauren said:
quote:

I used to post regularly on the Lyme Friends website when I first began my Rife journey and I was torn apart by someone much in the same manner that you're tearing apart Catskill now. I'm wondering if you're the same person? Of course if you are you won't speak up and say so, so I suppose that's neither here nor there.

No, it wasn't me. I have never joined that group....I don't even go there to read either. I barely post here as you can see from my whopping 112 posts to date over a five year period.

Dig down a little deeper in your past, and I'm sure that you can find a few more bitter memories that you can heap on my back as well. Maybe a little psycho analysis will help. Maybe it will help to put an end to your need to continually lash out at others when they disagree with you.

You use the term ``torn apart'' to describe what happened to you and catskill both. I didn't see what happened to you over there, but I doubt if it's an accurate description of what really happened, based on what I wrote here. All I did was to give actual proof of what she claimed, and what she did in reality. It was all matter of factly laid out. I didn't attack her character as a whole, or try to make her out as some kind of evil person like you are trying to do to me. I attacked her argument with her own statements, because that's what people need to see.

Why is it necessary to use a real example? Because rifers believe that experience is king, and that no one's opinion means didley unless they have actually used it. It isn't enough to give examples from people that have found rife to be useless; it has to be first hand information from actual experience. But it doesn't stop there; if there are negative testimonies against rifing, well there has to be a reason like operator error or machine malfunction. And then finally if all else fails, attack the person and try to discredit their testimony as you and others have tried to do in this thread.

Posts: 132 | Registered: Jul 2005  |  IP: Logged | Report this post to a Moderator
METALLlC BLUE
Frequent Contributor (1K+ posts)
Member # 6628

Icon 1 posted      Profile for METALLlC BLUE     Send New Private Message       Edit/Delete Post   Reply With Quote 
Why was this post brought back up again with the same posts as it had a week ago?

Either way, I saw my LLMD yesterday (Dr H in NY). They are encouraging me to use Rife now. They said "We have a routine for people who Rife that will support your treatment. The Rife is your decision, we don't know or suggest frequencies, but we can provide plenty of help in detox, heavy metals, and many other areas.

This was a shock to me. It was the PA who I saw and have worked with. She is brilliant. She did "not" prescribe or recommend this to me, but she seemed excited and happy about my decision to take it seriously.

At any rate I'm exhausting a few more antibiotics before starting. She prescribed ongoing Rifampin, Tindimax, Naltrexone, RX Chelex, Vitamin D3, Milk Thistle, Vitamin B6, (Multi Mineral), Lariam, Magnesium, Diflucan or VFEND, Ongoing Nystatin, VSL3/Theralac/Saccrymycin, ALA, and NAC, as well as Dr. Zhangs Hepa#2.

She also told me to get a Reverse Osmosis unit installed for fresh water. She told me I need to drink a lot, especially when I begin Rife. She told me once I'm done with the antibiotics, then I can start Rife if I choose.

Anyway, I thought this was exciting news since I'd never heard her so excited about Rife before.

--------------------
I am not a physician, so do your own research to confirm any ideas given and then speak with a health care provider you trust.

E-mail: [email protected]

Posts: 4157 | From Western Massachusetts | Registered: Dec 2004  |  IP: Logged | Report this post to a Moderator
Sheryl777
LymeNet Contributor
Member # 17804

Icon 1 posted      Profile for Sheryl777     Send New Private Message       Edit/Delete Post   Reply With Quote 
Metallic, please let us know if they seem to like one machine better than another or whether they like several. They might not be able to state that for fear of the law. I mentioned to my LLMD that I was interested in rife, specifically an EMEM, but he didn't comment on it although he said a lot of people were helped by rifing.

Sheryl

Posts: 258 | From Spokane, WA | Registered: Oct 2008  |  IP: Logged | Report this post to a Moderator
METALLlC BLUE
Frequent Contributor (1K+ posts)
Member # 6628

Icon 1 posted      Profile for METALLlC BLUE     Send New Private Message       Edit/Delete Post   Reply With Quote 
They do not support any particular machine.

--------------------
I am not a physician, so do your own research to confirm any ideas given and then speak with a health care provider you trust.

E-mail: [email protected]

Posts: 4157 | From Western Massachusetts | Registered: Dec 2004  |  IP: Logged | Report this post to a Moderator
JR
LymeNet Contributor
Member # 16898

Icon 1 posted      Profile for JR     Send New Private Message       Edit/Delete Post   Reply With Quote 
"Who hasn't rife helped?"

Rife didn't help me one bit.

Posts: 365 | From Sylvania | Registered: Aug 2008  |  IP: Logged | Report this post to a Moderator
IckyTicky
Frequent Contributor (1K+ posts)
Member # 21466

Icon 1 posted      Profile for IckyTicky     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hasn't helped me because I have not been able to try it yet... that said, I have a personal friend who recently cured his own cancer using only rife.

--------------------
IGM: 18+, 23+, 30+, 31+++, 34+, 39IND, 41++, 58+++, 66+, 83-93IND
IGG: 31+, 39IND, 41+
Also positive for Mycoplasma Pneumoniae and RMSF.
Whole family of 5 dx with Lyme.

Posts: 1014 | From Texas | Registered: Jul 2009  |  IP: Logged | Report this post to a Moderator
springshowers
Frequent Contributor (1K+ posts)
Member # 19863

Icon 1 posted      Profile for springshowers     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hello Icky.. Thats great news..
Does that person have a blog or a place they told their story?

I am trying to introduce this to my mother as a possiblity for her cancer treatment and a success story would be a nice thing to be able to read..

Thanks Let me know .

Posts: 2747 | From Unites States Of America | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
tick battler
Frequent Contributor (1K+ posts)
Member # 21113

Icon 1 posted      Profile for tick battler     Send New Private Message       Edit/Delete Post   Reply With Quote 
For those of you like JR and wildcondor and others who say rife has not helped them, it would be so helpful to hear the details of your experience.

Can you share what machine you used and how often you used it and how long your sessions were and whether you herxed during or after it?

This is the type of info that would be really helpful.

Thanks,
tickbattler

Posts: 1763 | From Malvern, PA | Registered: Jul 2009  |  IP: Logged | Report this post to a Moderator
JR
LymeNet Contributor
Member # 16898

Icon 1 posted      Profile for JR     Send New Private Message       Edit/Delete Post   Reply With Quote 
Rife never helped me because I never rifed. [Razz]

I followed Dr. B's guidelines and was treated for about 2 years. All better now.

Posts: 365 | From Sylvania | Registered: Aug 2008  |  IP: Logged | Report this post to a Moderator
j_liz
LymeNet Contributor
Member # 20496

Icon 1 posted      Profile for j_liz     Send New Private Message       Edit/Delete Post   Reply With Quote 
I just scanned the posts quickly, so I may have missed this...

I was surprised that nobody mentioned "THE CANCER CURE THAT WORKED". I am told that Dr. Rife did prove rife in the court trial mentioned (post said one patient died).

liz

Posts: 472 | From NJ | Registered: May 2009  |  IP: Logged | Report this post to a Moderator
tick battler
Frequent Contributor (1K+ posts)
Member # 21113

Icon 1 posted      Profile for tick battler     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, I just saw the documentary about Rife. He did cure something like 13 out of 14 terminally ill people from cancer using his machine.

Have you read the book you mentioned above, liz? I am considering getting it.

See my recent thread about how to get the documentary if you want to watch it. I found it fascinating.

tickbattler

Posts: 1763 | From Malvern, PA | Registered: Jul 2009  |  IP: Logged | Report this post to a Moderator
j_liz
LymeNet Contributor
Member # 20496

Icon 1 posted      Profile for j_liz     Send New Private Message       Edit/Delete Post   Reply With Quote 
My sis and I have gone halve-sies on a couple of Lyme books, it is one of them. She read it and was very excited about it. I haven't read it, because of my brain fog, but I may be able to read it now. Maybe when hubby picks up my Rife machine he can get that for me, too.

I am going to check out your other post about the docu. Sorry, I didn't get back to you sooner. I hadn't marked to get emails notification, I have now.

liz

Posts: 472 | From NJ | Registered: May 2009  |  IP: Logged | Report this post to a Moderator
Marnie
Frequent Contributor (5K+ posts)
Member # 773

Icon 1 posted      Profile for Marnie     Send New Private Message       Edit/Delete Post   Reply With Quote 
Rife therapy, to work, requires the RIGHT frequency (scanned and pulsed) for the right amount of time using the most powerful machine made (which increases the depth of penetration).

It takes many treatments to be effective just as it takes MULTIPLE HBO "dives" to work...along with reducing inflammation simultaneously.

Bb is camped out in the MEMBRANES...very specifically the "basement membranes". Google that and see where they are.

Because it is so close to blood vessels, lyme becomes a vascular problem. "H16" is the category.

Healing takes TIME.

If antibiotics (alone!) worked, a few "rounds" should do the job.

Heating is key...how we heat the infected cells via "frequencies" or "lightwaves" or other means is key.

When our own defense cells are infected, Bb makes them "cold" and in we send the "de-icer" NaCl to Bb's pleasure...as it needs NaCl for motility and has a gene for Na-ATPase which does this: ATP-> ADP.

The infected cells are functioning solely on glycolysis (glucose for energy) and maybe becoming "immortal" (HeLa) cells.

Not good.

Bb triggers TNF alpha and (worse) IL1 B which together, in time will do a number on your pancreatic cells.

IL1 B blocks insulin release which activates an enzyme called PFK which Bb is dependent on....

Up goes glucose.

Many lyme patients develop diabetes, hypothyroid, etc., etc.

Porshe, do you know HOW your microwave oven works to heat foods (esp. those loaded with glucose)? Microwave ovens use frequencies.

And my Advantium oven cooks/heats with the "speed of light".

Before you try to say there is nothing to far infrared therapy too, you might want to look at this:

Recruiting Far Infrared Irradiation for Control, Management and Treatment of Amyotrophic Lateral Sclerosis (ALS)
Condition: Amyotrophic Lateral Sclerosis
Interventions: Radiation: Far Infrared Radiation (5μm to 20μm wavelength); Radiation: Far infrared radiation

Recruiting Far Infrared Irradiation for the Management, Control and Treatment of Frontotemporal Dementia
Condition: Pick Disease of the Brain
Intervention: Radiation: Radiation: Far Infrared Radiation (5μm to 20μm wavelength)

Recruiting Energy Specific Far Infrared Radiation Treatment for AIDS
Condition: HIV Infections
Interventions: Radiation: Far infrared; Radiation: Far infrared radiation

Recruiting Far Infrared Irradiation for Stroke Rehabilitation
Condition: Stroke
Intervention: Radiation: Far Infrared Radiation

Recruiting Far Infrared Irradiation for Management and Treating of Parkinson's Disease (PD)
Condition: Parkinson's Disease
Intervention: Radiation: Far Infrared Radiation (5μm to 20μm wavelength)

Recruiting Far Infrared Irradiation for Managing, Control and Treatment of Huntington's Disease (HD)
Condition: Huntington Disease
Intervention: Radiation: Far Infrared Radiation

Recruiting Far Infrared Irradiation for Managing and Treating Multiple Sclerosis (MS)
Condition: Multiple Sclerosis
Intervention: Radiation: Far Infrared Radiation (5μm to 20μm wavelength)

http://clinicaltrials.gov/search/open/intervention=radiotherapy

We are entering a new time. We WILL be using soundwaves and lightwaves to heal. It is coming fast.

Rife:

http://www.rife.de/files/smithsonian.pdf

Scroll down to page 208 near the bottom...

Posts: 9481 | From Sunshine State | Registered: Mar 2001  |  IP: Logged | Report this post to a Moderator
map1131
Frequent Contributor (5K+ posts)
Member # 2022

Icon 1 posted      Profile for map1131     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thank God. That's not just for us with lyme & company. There's this "C" disease that we must have change in treatment protocols.

Pam

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

Posts: 6495 | From Louisville, Ky | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
  This topic comprises 3 pages: 1  2  3   

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.