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Hi Fab. What is the placement of patient with respect to the old diathermy output. Is the output those two angled antenna arms or is that for climbing sparks. And what about for in vitro vials.Quote:
Originally Posted by Fabrizio del Tin
I have some confusion because an alternative concept
Could have a spark device discharging into a gas tube as a terminal load . Didnt rife always use plasma tubes ??? Any thoughts? ??
Old diathermy is similar to Violet Ray. You also have similar electrodes. You can use effluvia on a short distance and even contact plates.
Violet Ray has one electrode in plasma and the charge must find earth. But all rifes tubes in old photos were not single tube . Maybe they never showed photos of the earlier apparatus. What do you think ?Quote:
Originally Posted by Fabrizio del Tin
Hello
The charge finds earth by ionizing air, creating ozone and nitrogen oxides (smells). Tesla coil, output voltage around 20,000 volts. Wave form very similar to the first Rife apparatuses. Damped oscillations.
Best regards
Diathermy machines have 2 poles, and they usually use a pancake coil for output at 150,000 V. But they also come with intermediate settings to have D'Oudin voltage and a lower voltage too, but at high current. You easily cook meat with the low voltage terminals.
Rife simply used the first transformer only of the 3. He custom wound it in order to have an output of 5,000 V.
That is just a little above the requirement to get helium full spectrum down to soft x-rays.
If you were to use argon, you need a much higher voltage (15,000 V should suffice).
The good advantage in using air, such as in violet wands, is that you can have a very broad spectrum. CO2 naturally has a broadband spectrum that resonates with microorganisms.
If you just use nitrogen oxide you obtain what Rife describes, matching treatment time and any other parameter. It can travel the flesh at depth at a magnitude smaller than radio wave speed.Quote:
Originally Posted by Jean Mareche
Hello,
I know these devices very well, having used them for decades for leak testing in glassware under vacuum (Holo electron devices) A potentiometer could be used to vary the output.
Best regards
Hi!Quote:
Originally Posted by Jeff Sutherland
This is only partially correct information. A cell can change its metabolism for other reasons as well:
- low osmotic potential of the cell membrane resulting, for example, from the wrong composition of lipids that make up the membrane
- for a small supply of oxygen to the cell fluids and inside the cell
- acidification of body fluids
This change in metabolism is built into the cell's defense mechanisms, which in this way begins to ferment glucose in the absence of oxygen, instead of burning it in oxygen. In this way, by consuming about 15 times more glucose, it manages to keep it alive.
Scientists have so far been concerned about the mechanism of cancer transmission to other organs, and this is where the BL theory works.
The immune system, which should eliminate such cells in the embryo, has an almost impact on the development of cancer, but sometimes it is so busy that it is impossible to locate and process all the signals.
What is the conclusion?
What is the consensus of specialists about the devices that can eliminate cancer? breast and bone?
From my experience Rife is not better than others in terms of success, but is better in terms of worsening things, Chemicals and radiations can produce cancer in a healthy individual, curing cancer with that is a bad approach.
All cases that i known treated in this way, have shorter or no longer life after diagnostic than untreated ones.
Cancer is time consuming, a visit a week at a Rife specialist not works, it need every day attention, more times a day, Rife alone do not do much.
All malignant cells have genetic mutations, this is the primary cause of cancer, immune system usually kill them before spreading, immunotherapy proved it`s value, but in most cases is not enough alone, Rife with immunotherapy is almost no experience, i can`t say that works.
Metabolic or hormonal disorders or altered environment can accelerate spreading of malignant cells but is unlikely that produce cancer by themselves, mutagens (chemicals and radiations) are proved to produce cancer, perhaps in early obscure stages of developing of a cancer altered environment may help malignant cells to survive and spread, by giving them a metabolic advantage and altering immune system`s effectiveness.
Agreed that there are other mechanisms that precipitate a cell into an anerobic state. I submit the only one that really matters in the case of cancer is the Rife BX BY organism infecting mitochondria and flipping the cell into an anerobic state. This sets up the cells for a carcinogen to start the random DNA mutations seen in cancer and the promoting agents to increase the rate of uncontrolled proliferation.Quote:
Originally Posted by Stanislaw Chmielarz
Mitochondria is a symbiotic organism has own DNA, relation with cancer is complex and almost unknown.
some studies:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779192/
One thing emerge from this document, malignant cell must have required energy to proliferate, in almost tumors mitochondrial regulation and function are preserved, nuclear genome mitochondrial control is preserved and cell eliminate mutant defective mitochondria.Some tumors are related with mutant defective mitochondria, but those cells simply have not enough energy to be so aggressive.
Signaling between mitochondria and host cell is complex.
Jeff,
The process that you describe makes cancer an intelligent process, an intelligent being so-to-speak, and not just some genetic defect that causes cells to proliferate. So, cancer becomes a complexity with its own instinct for survival and living process. Its own DNA.
Your described "flipping the cell into an anerobic state" would be the result of a DNA hybridization which would result in a new being. A parasite.
Industrial fermenting processes utilize the bacillus litcheniformis microbe in order to "flip the cell into an anerobic state" if I am stating this correctly.
I was just thinking that it would be a simple enough process to place some bacillus L. onto a microscope slide and expose it to frequencies ?
dj
The consensus among the leading scientists when I was getting my Ph.D. in Carcinogenesis was that cancer was an evolutionary innovation that enabled the animal to stay alive long enough to reproduce in a toxic environment. So in that sense it is an intelligent process.Quote:
Originally Posted by Dan Jenson
Hi all:
The response to the question is YES but!!.
To achieve the best results the set up is of primary importance.
I learned it in the daily doing.
You have to have the following:
1- Body temperature measurement and recording, hardware and software from PicoTech.com.
You need this device to SEE what is taking place in the Clients body while you apply Rife frequencies.
It will take you some 5-6 sessions before you can handle the temperature levels with confidence.
You have to measure body temperature with a resolution of 0.01C, customize Pico Log to this level.
What you measure is RATE of change. You can NOT compare true temperature between different people.
Temp. will raise after killing the bacteria from .02 to .15C or more, with a Std time of 2min 15 second. This is an average don't take it as the rule, some bacteria's brake at 4 min!!!
Keep notes of freq. and temp., for comparison between sessions, very important.
Watch for common frequency like the 880.
No Bacteria present NO temp goes up for that frequency.
The ideal outcome is: you pass all the freq. and temp increment is zero. that is the end of treatment!!
2- I use a 27Mhz system with linear lamp of 52 cm, I made several lamp in Neon shop until I got the right gas pressure.
The Rife treatment is not the only thing you have to take in account.
I started with cats and dogs to see if it worked, and all OK, and I follow with humans.
Treatment: Almost 2hr Lamp session, 3 times a week, for three weeks.
Sugar is forbidden, same for Carbohydrates (no visits to the bakery) and Alcohol. Eat Alkaline food.
The surprise: Some People came back from his Doc routine control after 3 month!! How is this possible???
After a week revising all the details I got the idea about the Bacteria eggs like Rife had, of how it reproduced, I looked at the reproduction time and found the answer. The reproduction time is 28 days!!!
After finishing the treatment next day bacteria eggs opens and lay new eggs "Goodby Lamp Work".
To solve this problem I used the Bob Beck Zapper, the Client should buy a Zapper and used it at home "every day" for 30 days to kill the new born Bacteria. If one day is skipped he should start all over again. For safety reasons he should use the zapper for two month.
Control: The client should come in for temperature control during week 3 of Zapper application. Zapper can fall and brake and not work. I control the zapper with an Oscilloscope.
I hope this comments can to increase Rife Technology to a higher degree of confidence.
HL
Hi Ionut,Quote:
Originally Posted by Ionut Nebel
During my reading of many researches and studies (I am not a specialist)
The human body is competent and able to heal itself without interference.
But the toxins (which you mentioned) surrounding us from every side impede the functioning of the body.
When cancer arises, yes, the immune system is the most important wall, and this wall cannot be destroyed by chemotherapy and radiotherapy.
But at the same time, a direct hit must be made to the place of the tumor, as (Royal Rife and other scientists) did.
Direct strikes to the tumor do not conflict with strengthening the immune system and cleaning the body with multiple programs that have proven to be effective.
I am completely convinced that the mechanism that Rife worked on .. targets the tumor directly (this is my hunch and not a scientific view frankly)
Hi Muath!
If You want to hit the tumor directly use 465MHz frequency but, a safe power is not known at this time(!).
very nice Horacio,Quote:
Originally Posted by Horacio Lange
I tried to translate your words accurately in order to fully understand everything you said.
What you have mentioned is very useful information.
The problem I have is that I did not get any device yet.
I am lost between the types and the high prices.
I am lost because I am (Arabic) and do not understand the accurate information because of Google Translate and because I am not specialized in these matters.
I am now linking information from here and there.
And I hope to get to something good
Hi Stanislaw,Quote:
Originally Posted by Stanislaw Chmielarz
sorry I embarrass myself because of my many (dumb) questions.
but this frequency (465MHz)!! How can I get it?
From what device?
and what do you mean (safe power is not known at this time(!).)?
Hi!
This frequency and its harmonics are used to detect cancerous tumors due to the increased absorption of this frequency by the cancer cells.
It can be used to overheat these cells and cause them to die.
Therefore, the necessary power is not known yet because it depends on many factors.
Diet plus iodine is safer, but the therapy must last for about 3 months.
I am at the stage of agreeing the test conditions and I have already built some devices.
Do I understand from your words that this frequency cannot be reached until this moment?Quote:
Originally Posted by Stanislaw Chmielarz
Can I get one of my friends who speak English and understand electricity to communicate with you? I desperately need a frequency to be effective in bone cancer
This must be a special device which can generate such a high frequency. Ordinary "Rife" devices, I know, cannot go as high.Quote:
Originally Posted by Muath Abuadas
So these devices are not capable?Quote:
Originally Posted by Stanislaw Chmielarz
like: john bedini (RPX) or Lakhovsky Multiple Wave?
So what is the solution?
INDIBA invests a lot of resources in researching its technology to ensure the best results. During this research, a team from the highly regarded Spanish University Hospital Ramón y Cajal in Madrid (Dr. Ubeda and his team) have been investigating what happens to the body's cells when INDIBA is applied. They have found that INDIBA's 448 kHz frequency is effective in stimulating stem cell proliferation and differentiation, and that normal healthy cells are not damaged in the process. Tests were also carried out on certain types of cancer cells in vitro, where it was found that the number of these cells decreased, but not the number of normal cells, making it a safe process to use on humans and therefore also on animals.
Muath, the closest we have to a true Rife is to use a plasma system of at least 60 watts, with transport or direct frequencies above 3.0 Mhz.
john bedini (RPX) is just a signal mixer, not a Rife.
Lakhovsky Multiple Wave is another technology, in general it helps the electrical repolarisation of the cells, but does not cure anything specifically.
a good device is expensive... for many technical reasons that require it, not the whim of the manufacturer...
unfortunately I haven't treated anyone for bone cancer, I don't know what can help.
to better understand what a Rife system is, here is the breakdown.
https://www.rifevideos.com/the_rife_machine_report.html
maybe the better machine for cancer is this: https://www.resonantlight.com/
I also visited this site beforeQuote:
Originally Posted by Carlos Palau
But what was missing from me
..is the advice of professionals like you.
Now I will strive to find the best solution
I thank you very much
I don't want to bother you any more, I don't want to bother you any more, but let me ask you, as I asked others:
About the possibility of contacting you with a friend who speaks English and has experience in this field to get accurate and truthful information?
I don't think there is a clear solution for this "cancer", it is more complicated than just having helicobacter .... I would try doctors who also use phytotherapy which is very powerful and beneficial.
Indiba is not Rife, but it is a very good piece of equipment that maybe someone has out there.
I don't do therapy, I only manufacture the equipment... and I'm sorry but I don't speak English.
I think all the summary knowledge about Rife is in Nenah Silver's book.
http://www.rifehandbook.com/
frequencies most commonly used in bone cancer
10025, 10026, 10027, 12000, 13280, 20080, 21275, 34000, 34048, 34096, 34240, 34320, 45872, 49040, 52808, 53376, 56384, 58752, 59408
really thank you CarlosQuote:
Originally Posted by Carlos Palau
These are general frequencies found on all machines on the market and the only known frequencies for bone cancer, as I said, unfortunately, there is very little research on frequencies for this particular cancer.
you can build your machine with components already tested by other users.
the spooky generator has a very comprehensive software and allows you to program your stuff and have it stored there without depending on the computer.
https://www.spooky2-mall.com/product...y2-generatorx/
control board and plasma tube coupling coil can be purchased assembled.
https://spectrotek.com/pa3.htm
https://spectrotek.com/lc31.htm
the plasma tube can be ordered from Canada, the best manufacturer on the market without a doubt.
8 inch Phanotron tube
http://billsplasmatubes.com/
any of us can give you some advice on frequencies, if you need to buy for the treatment you can order them from us:
https://www.dnafrequencies.com/human-diseases
hi CarlosQuote:
Originally Posted by Carlos Palau
You helped me so much
And I started searching in my country for some specialists
to make the right device.
I have kept all the links you sent me.
I will tell you every progress I can make
You have given me a lot of explanation
As I told you, I will send this information to the specialist when I find him.Quote:
Originally Posted by Carlos Palau
But just to be a little more understandable:
These tools and devices have to be grouped together to reach the greatest possible help and impact?
yes, as listed, you get a 3.1 or 3.3 Mhz Carrier Rife, depending on the order, a complete set.
However, you need a good assembly technician.
if you need help, just ask us.
This is incredible information indeed. I've been trying to figure out myself which route to go and the genX (with the software ) - SPA5 - LC3 - 8 inch Phanotrom tube from Bill seems like a good option. Has anyone ever measured the output of a GenX ? is it consistent - putting out what it's supposed to be? I'm scared it's doing something other than what it says.
Is there any downside from a technical point in using a good sound card + Fredx as the generator instead of the Genx+software? Just curious.
PA3 Rife Plasma Tube Amplifier and LC31 is totally complete for what you need.
The genx is very accurate, and can handle higher frequency ranges, in my experience the 3.3Mhz carrier range is best suited to frequencies from 20000 to 70000 Hz.
If you don't mind relying on the computer you can buy the basic $100 spooky one.
Treating cancer is a time consuming endeavour you can try a frequency/set it may work some time, you need find other and other, i had no success perhaps some ones made it.
When cancer goes clinical time is gone, is already a multitude of clones of malignant cells, early detection is important, I no agree to use chemicals and radiations in any stage of cancer, especially in early cancer,
Very important, patient must stop eat meat, this thing alone can be stop evolution to clinical cancer.
Early detection by frequency was discussed in this forum, now are available PCR test that can detect cancer years before goes clinical.
As we discussed earlier cancer seems to an integrated entity not a collection of mutant cells, cancerous cells preserve most important systems as aerobic respiration, adhesion, signaling. tumor can a parasitic organism.
Another approach in cancer is to limit growth speed in a hard way, by limiting protein and manufacturing capability.
Normal cells do not use that machinery at full speed, but if is slowed down normal cells use it close the new limit, malignant cells lose that advantage, even if run that machinery at full speed (hard way slowed).
A way do to this is to break ribosomal complex by frequency, escaping mutations are unlikely, this is a long term evolution system, it has very few working variants.
If yow if you make immune system to recognize tumor as non self after you slow it down in hard way you may cure cancer.
I will add some important weaknesses of cancer cells:
- the LD50 index is much lower for cancer cells than for healthy cells
- cancer cells stop multiplying in an alkaline environment, various therapies use it (honey-cinnamon, maple syrup - soda)
- cancer cells have lower resistance to high temperature than healthy cells (oncothermia)
- cancer cell complexes absorb 465MHz, so they can be detected and destroyed by overheating
- a method based on a urine test to determine whether the body has a cancerous process developed by a doctor from the Philippines has been known for a long time
Hi StanislawQuote:
Originally Posted by Stanislaw Chmielarz
Does this test have a specific name?
Tried searching for it on google
It seems that it is not available in all places?
I know that some chemicals related with cancer can be detected by trained dogs in urine, sweat, respiration, or simply smelling that person, but PCR proved more sensitive and is routinely available, detection is as least 3 years in advance to go clinical it finds transcripts of genes used by cancerous cells and not used by normal cells.
In cancer management you may consider systems evolution, some parts of genome are highly conserved, same information for more than 1 billion years, revealed by extensive sequencing of DNA of many species.
About 465MHz is easy to generate but i have no experience, i purchased some broad band power d mos fets up to 2 Ghz, 100w, even I was a child 30 years ago I generated some w in that band, now i see is perfectly possible to use a fiber laser as carrier, and target tumors.
That was developed by Manuel D. Navarro, M.D.
It's called HCG Urine Immunoassay.
Check out navarromedicalclinic.com
It is now run by his son, Efren Navarro, M.D.
---Paul Roxas, Philippines
Seems like they are no longer doing HCG testing anymore. Any other folks doing this in the USA?
Do you have any advise on frequency for a GIST tumor. I started at frequency 2008, then advanced to 2128. However, neither frequency has shrunk the tumors. I still believe that the machine works, it's just this cancer is a bit rare so there's no data out there. Thanks for your input.
Hello.
I would start treatment with flukes - intestinal fluke and fluke of the pancreas and liver - min. 30 minutes each, frequencies of Hulda Clark and Ch. Boehm. Then - Trichomonas and Helicobacter Pylori. Also Actinomycosis, Candida, Aspergillus. There can be many reasons - you need to look for the reason. Try R. Rife's original frequencies. What device do you have?
You also need to undergo an antiparasitic course of treatment.
I'm not sure what you mean by "flukes", this type of cancer is a sarcoma not a parasite. I have a coiling machine build by "Doug Coil Machines", it's an amplified frequency generator. I have been tested for H. pylori and it's negative. I have had a ton of genetic testing on my blood and the original specimen removed in 2020 and doctor's are baffeled as to the reason. Thanks for your reply.
Frequency 2008 is a 10-fold reduction in the sideband frequency for sarcoma - 20080, R. Rife and F. Hoyland. It operates only as a sideband with a carrier frequency of 3.3 MHz. But for this you need M.O.P.A. with plasma lamp. Just running the 2008 frequency won't do anything and Doug Coyle can't cure cancer. It's my opinion.
And about the role of parasites in the formation of cancer, read the works of H. Clark.
Cancer is a combination of several types of pathogens - for carcinoma, this is at least 2 pathogens (for example: bacteria + protozoa), and for sarcoma - at least 4 pathogens, so sarcoma is not treated and has never been treated - few people understand the reason for its formation. And since it is very difficult to diagnose pathogens, you need to act by the method of elimination - destroy pathogens sequentially: 1. first - parasites, because they are reservoirs for storing fungi, bacteria and viruses.
2. then - the protozoa.
3. then - fungi.
4. bacteria.
5. viruses.
Frequencies alone are NOT ENOUGH for sarcoma!
But you can do as you see fit.
Let's look at it from a different angle.
Cancerous cell changes can be detected and removed at an early stage by the immune system, but this immune system must have "free processing capacity" and if it is busy keeping larger numbers of pathogens in check, it simply cannot cope and the pathogens take over. Similarly with cases of activation of pathogenic bacteria during any "viral" infection.
Quote:
Originally Posted by Yuriy Vladimirovich
Thanks, Yuriy...I had someone else tell me something similar. So I have added Ivermectin, Febendazole (for parasites) and Peach Tree Extract (for molds) along with going back to frequency 2008 but increasing my time on the machine. I appreciate your input! PS: Keeping Ukraine in our prayers!
Thanks for your input Stanislaw. I believe what you are saying. I had been cancer free for almost 4 years, but had several surgeries (unrelated) last year. My hip surgery caused a fat emboli in my lungs, that lead to a heart attack. All is fine now with no heart damage. Then another surgery just a couple months later. I believe this put too much stress on my whole body and it could not fight off the cancer. I have added Ivermectin, Febendazole and Peach Tree Extract (for mold) to my regiment and lastly, I'm going back to coiling at 2008. I am also taking a much harder look at my diet. Even though I've lost weight, I still eat too much sugar! So I'm hoping all of this combined will allow my body to become strong and along with coiling, will be abel to fight this cancer. Thank you again and God Bless!
What is the maximum frequency your device can produce? I believe that the higher the frequency, the better.
Higher frequencies can be better. Higher frequencies can be used on lower frequency machines by calculating and using the lower harmonic frequencies of the higher frequency.Quote:
Originally Posted by Yuriy Vladimirovich
Also, sweeping around a frequency can be useful. And varying the wave form can help, for instance changing from sine to square form.
Hello
Changing the waveform is changing number and relative amplitudes of harmonics, playing with the Fourier transform. With a generator able to construct the waveform (from a lookup table) you can make whatever you want.
Best regards
Thank all of you for your responses. Unfortunately, most of your suggestions are far beyond my knowledge. I do know my machine only goes to 2200. One of the major issues I believe is I've been coiling in the wrong area because the MRI report was mis-leading in it's description. I have gone back to 2008 frequency for sarcomas, used a better placement of the coil and have continued to up the time to 10 minutes every 3rd day...in addition, I have added Ivermectin, fenbendazole and gone on a strick KETO diet. Hopefully this will help boost my immune system while killing the cancer! Thank you all again!
2200 is the highest...
Greetings. I am a new member with a diagnosis of advanced endometrium cancer that has now moved beyond the uterus. I have a GB-4000 and have used one of the channels called Endometrium Cancer but would like to have more protocol and how to use the machine most effectively, frequency of use, is a channel more effective than sweeping, the authors of the channels are unknown and very much hoping that the quote by Charles Claessens:
If you don't get enough power at the right frequency to the tumor, you end up stimulating the cancer into growing more, rather than killing it, just as Rife said. would not apply!
Any advice would be appreciated.
Thank you,
Amy
Hi.
Use general Rife frequencies for cancer and sarcoma - 1607450 Hz, 11780000 Hz, 1529520 Hz, 1143000 Hz - all these frequencies are in the book and are included in the programs.
The cause of tumors can be infection with various pathogens.
They are difficult to diagnose, so you can use the method of exclusion.
If you do not understand how to act, look for a good specialist - you will not cope on your own, you will only waste time.
Cancer is not a place for experiments.
GIST [Gastrointestinal Stromal Tumor]: 0.12, 0.2, 0.9, 47.5, 5.26, 127.25, 335.91, 487.5, 692.49, 752.01 - in KHz ( x 1000)
Endometrial Cancer: 0.35, 0.93, 12.33, 25.23, 35.69, 87.5, 93.5, 233.63, 434, 519.34
Endometrial Polyps: 1.22, 3.27, 4.23, 6.87, 9.03, 74.05, 103.83, 274.35, 388.32, 482.23
Endometrioma [Ovary]: 0.13, 0.57, 0.78, 12.27, 68.29, 135.25, 272.72, 425.53, 733.91, 836.42
Endometriosis [Ovary]: 0.13, 0.57, 0.78, 12.27, 68.29, 355.72, 434.15, 571, 839, 932
- in KHz ( x 1000)