Aerosol Infection by Flu Viruses

Photo by Kickstarter Michael Gilvary Sick Building Project – view here

For years Frequency Foundation has been reporting on flu virus aerosol infection. Many of these infections are caused by airborne parasites where masks can block large particles. However, for virus particles of a few microns, masks are ineffective. This came to a head in COVID when it became clear that medical scientists do not understand basic physics. See https://www.wired.com/story/the-teeny-tiny-scientific-screwup-that-helped-covid-kill/

Frequencies are mathematic data that do not lie. They are present in a building or not. Frequencies sent to the building consistently reduce infection 100% of the time. You do not need a clinical trial to show this after you do it on hundreds of buildings with 100% success (in at least reducing infection if not eliminating it).

Furthermore, if you are skeptical, it only takes a few weeks on your building to prove it either helps or does not help. The alternative is to live with the infection continuously.

Conventional flus, spread by aerosol parasites, were radically reduced during COVID with masks, despite the propaganda masks were ineffective in stopping the COVID virus. The 6 foot separation was also a myth that has been debunked in the science journals. Do your own research. There is real data out there.

Here we just want to emphasize that aerosol infection is one of the primary routes of viral infection, particularly for COVID, and buildings that are not properly ventilated with air cleaners that kill viruses become infected. There are many companies that do sick building remediation but they are expensive and your local Starbucks, Whole Foods, Home Depot, and other vendors are not using them every week. A single really sick person can infect a store that does not have air clearers and ventilation that kill viruses and other pathogens quickly.

This is why we have the “Sick Building Service” for weekly scans for $99/month. We have many individual subscribers for home that are infected as people are well aware that mold is a critical issue. When we scan buildings using the same technology we use for people we find viruses, bacteria, and many other things in addition to mold. It is so inexpensive that some of our homes use this service every month, continuously.

It is critical for health clinics and restaurants to be aware of the Sick Building Service because these are the areas that become most infected, most often, by the most people. We find the same thing in retail and wholesale stores. Clearing these buildings with frequencies not only prevents infection of customers and employees, it significantly changes the atmosphere in the store make it feel more friendly. People linger longer and buy more products as one of the largest retail furniture outlets in Hawaii discovered.

Monkey Pox

Clinicians have been asking about Monkey Pox so Frequency Research Foundation investigated. In addition to identified cases there appears to be low level asymptomatic infections in the general population. There have been previous outbreaks in the United States so there are old strains as well as new strains.

Monkey Pox has been wargamed at the 2021 NTI Munich Security Conference who predicted an outbreak on 15 May 2022 so it is arriving right on schedule.

For pathogens of public health concern, Frequency Research Foundation provides frequencies found to be useful for researchers under a Creative Commons share and share alike license. This means you can use it freely when citing it’s source and if you find a way to make it better you must share that.

Researches are well aware that frequencies can be both helpful and harmful and testing is required to see if frequencies are applicable. We make no warrantees and you use these frequencies at your own risk for research purposes only. Diarrhea has been noticed on occasion when running these frequencies.

We do commit to upgrade them if you have photos of an infection where the frequencies are not working. We will post these frequencies free for subscribers along with updates as they are improved. You might subscribe to make sure you get notified of the updates.

Frequencies are provided in F100 script language which will run directly on any F100 type device. For running these frequencies on Spooky2 hardware you can put them in the Spooky2 Tools translation program on this web site. For more information on how to use these frequencies see the Frequency Research Foundation FAQ available with all product downloads.

#monkey pox
#copyright 2005-2022 Frequency Research Foundation, USA. Offered for license under the Attribution Share-Alike
#license of Creative Commons, accessible at http://creativecommons.org/licenses/by-sa/4.0/legalcode and
#also described in summary form at http://creativecommons.org/licenses/by-sa/4.0/. By utilizing these frequencies
#you acknowledge and agree that you have read and agree to be bound by the terms of the Attribution ShareAlike
#license of Creative Commons.
repeat 4 #more repeats will be needed as 4 repeats are for highly tuned DMI/SG2 systems with DNG photos
dwell 90
program c
vbackfreq a 0.049787068 0 71.5
vbackfreq b 0.090909090 0 71.5

#monkey pox 20220521
fuzz .002% 2
54545454 44545454 35454544 24545454 20454545
19445454 18676767 17454545 16454545 15454545 14454545 13454545 12454545 11454545
10454545 9454545 8454545 7454545 6454545 5454545 4545454 3445454 2445454 1676767
fuzz .044% 1
967676 845454 745454 665454 645454 545454 465454 445454 313654 267676 154544 96767 84545 74545
fuzz .044% .2
66767 54545 44545 34545 24545 14545 9454 8454 7454 6676 5454 4454 3545 2454 1454
fuzz .044% .1
945 854 767 654 554 467 354 267 154

#monkey pox 20220521
fuzz .002% 2
56767676 44545454 34545454 24545454 20454545
19454545 18454545 17454545 16454545 15454545 14454545 13454545 12454545 11454545
10445454 9545454 8545454 7454545 6455645 5454545 4754545 3545454 2454544 1445454
fuzz .044% 1
945454 867674 754546 685454 667676 545454 465454 431354 367676 245454 167676 95454 86767 76767
fuzz .044% .2
65454 56767 46767 34545 24454 16767 9667 8545 7545 6545 5454 4545 3676 2676 1676
fuzz .044% .1
945 854 745 654 554 467 354 245 154
goto end

#monkey pox cataract 20140923 20181218 20190427 20190519# 20190806 20220521
fuzz .002% 2
57864356 44554545 36554543 24454345 20454345
19434545 18454545 17454547 16345454 15454345 14545454 13545444 12543454 11454545
10445454 9454545 8545454 7545454 6545584 5454545 4754545 3545454 2545454 1545454
fuzz .044% 1
954655 845454 754545 664545 645454 554545 464545 445454 313454 245434 154545 94545 84545 75454
fuzz .044% .2
64543 54545 44545 35444 25434 13454 9454 8454 7545 6454 5545 4454 3545 2545 1543
fuzz .044% .1
945 877 745 667 567 454 345 245 145
goto end

label end
end repeat

Viruses Are Constantly Floating Down Through the Atmosphere

Deposition rates of viruses and bacteria above the atmospheric boundary layer

The ISME Journal (2018)
doi:10.1038/s41396-017-0042-4
Download Citation
- Microbial ecology

Abstract

Aerosolization of soil-dust and organic aggregates in sea spray facilitates the long-range transport of bacteria, and likely viruses across the free atmosphere. Although long-distance transport occurs, there are many uncertainties associated with their deposition rates. Here, we demonstrate that even in pristine environments, above the atmospheric boundary layer, the downward flux of viruses ranged from 0.26 × 10⁹ to >7 × 10⁹ m⁻² per day. These deposition rates were 9–461 times greater than the rates for bacteria, which ranged from 0.3 × 10⁷ to >8 × 10⁷ m⁻²per day. The highest relative deposition rates for viruses were associated with atmospheric transport from marine rather than terrestrial sources. Deposition rates of bacteria were significantly higher during rain events and Saharan dust intrusions, whereas, rainfall did not significantly influence virus deposition. Virus deposition rates were positively correlated with organic aerosols <0.7 μm, whereas, bacteria were primarily associated with organic aerosols >0.7 μm, implying that viruses could have longer residence times in the atmosphere and, consequently, will be dispersed further. These results provide an explanation for enigmatic observations that viruses with very high genetic identity can be found in very distant and different environments.

SV40 Virus Frequencies

Recent work on multiple cases of SV40 with related cancers led to significant updates to multiple strains of the virus using the latest frequency templates. Each virus strain has over two dozen frequencies which target the virus, all of the components of the machinery for the virus, the DNA of cells contaminated with the virus, and the energy system of the human body which is distorted by the virus. All frequencies are available to subscribers.

[trx_button type=”square” style=”filled” size=”small” align=”center” link=”https://www.frequencyfoundation.com/product/sv40-version-2-0/” popup=”no” top=”inherit” bottom=”inherit” left=”inherit” right=”inherit”]SV40 Frequencies[/trx_button]

Bookchin, D. and J. Schumacher (2004). The Virus and the Vaccine: The True Story of a Cancer-Causing Monkey Virus, Contaminated Polio Vaccine, and the Millions of Americans Exposed. New York, St. Martin’s Press.

Everyone infected with the SV40 virus should read this book and that includes at least 100 million Americans. The contamination of polio vaccine with the carcinogenic SV40 virus apparently continues even today in some cases. Information on the most carcinogenic of all viruses and its connection with polio vaccine has been systematically suppressed since the 1960’s. Careers have been threatened, some destroyed, others altered dramatically. Funding for investigating what will come to be known as one of the greatest public health problems of the 20th century is still severely restricted.

The authors original article in the Atlantic Monthly (Feb 2000) has been expanded into a riveting book that reads like a novel. Extensively documented, it includes a complete bibliography of all research on SV40 and notes from interviews of every major player in this controversy who is still alive. The story would make a great episode for the X-Files and you might never look at the NIH in quite the same way again. The 2004 controversy over NIH officials acting as consultants for the drug companies is only the tip of the iceberg.

Char Boehme published a set of frequencies on the Rifers list ([email protected]) developed from available DNA sequencing data. I have tested her frequencies against a known SV40 infection and they all test positive, demonstrating the value of DNA sequencing data and her technique. We both view this as a widespread public health problem generated by contaminated vaccines.

Parasites are often infected with SV40. When you kill them, they release more SV40. You may need to repeatedly clear your system of this virus after killing parasites. In addition, when killing cancer cells in SV40 induced tumors, the virus will be released and cause reinfection. Run SV40 frequencies after killing SV40 induced tumor cells. Finally, a magpulser will stimulate virus production in infected cells and this must be dealt with.

On review of the medical literature, there are clearly multiple forms of SV40. One mutated form cannot replicate and there are others. See:

Simian virus 40 (SV40) DNA replication: SV40 large T antigen unwinds DNA containing the SV40 origin of replication. Dean FB, Bullock P, Murakami Y, Wobbe CR, Weissbach L, Hurwitz J. Proc Natl Acad Sci U S A. 1987 Jan;84(1):16-20.

Complete nucleotide sequence of SV40 DNA.
Fiers W, Contreras R, Haegemann G, Rogiers R, Van de Voorde A, Van Heuverswyn H, Van Herreweghe J, Volckaert G, Ysebaert M. Nature. 1978 May 11;273(5658):113-20.

The determination of the total 5,224 base-pair DNA sequence of the virus SV40 has enabled us to locate precisely the known genes on the genome. At least 15.2% of the genome is presumably not translated into polypeptides. Particular points of interest revealed by the complete sequence are the initiation of the early t and T antigens at the same position and the fact that the T antigen is coded by two non-contiguous regions of the genome; the T antigen mRNA is spliced in the coding region. In the late region the gene for the major protein VP1 overlaps those for proteins VP2 and VP3 over 122 nucleotides but is read in a different frame. The almost complete amino acid sequences of the two early proteins as well as those of the late proteins have been deduced from the nucleotide sequence. The mRNAs for the latter three proteins are presumably spliced out of a common primary RNA transcript. The use of degenerate codons is decidedly non-random, but is similar for the early and late regions. Codons of the type NUC, NCG and CGN are absent or very rare.
______________________________________________

There is a new article out on the connection between cancer and the SV40 virus which is widely distributed in the human population because of polio vaccination contamination. NCI has followup studies on Army “volunteers” who were given contaminated polio vaccine in 1960-61.

Testing a volunteer (who was in the Army and given the vaccine in 1960) with a liver tumor and a history of melanoma and multiple basal cell carcinomas showed SV40 distributed throughout all organ systems. Plate zapping organ by organ was required to root it out.

I’ve noticed SV40 in several other cancer patients. Electronic medicine researchers should check each other for presence of this virus and eradicate it. SV40 causes cancer in lab animals, causes cells to become immortal in vitro, and is found in human tumors. It inactivates genes related to controlling cancerous growth. SV40 antibodies are present in 3-4% of the population. SV40 can start a tumor growing including cells that are not infected with HIV. The uninfected tumor cells have a selective growth advantage and replace infected cells, caused the SV40 virus to disappear. This stealth phenomena is one of the reasons it has been difficult to conclusively state that SV40 is causing cancer. However, for some tumors, the evidence is far stronger than smoking.

Simian virus 40 in human cancers
Regis A. Vilchez MD, Claudia A. Kozinetz PhD, MPH, Amy S. Arringtonc, Charles R. Madden PhD and Janet S. Butel PhD
The American Journal of Medicine Volume 114, Issue 8 , 1 June 2003, Pages 675-684

Abstract

Background
Many studies have reported the presence of simian virus 40 (SV40) deoxyribonucleic acid (DNA) or protein in human brain tumors and bone cancers, malignant mesothelioma, and non-Hodgkin’s lymphoma. However, the small samples and lack of control groups in some reports have made it difficult to assess their reliability.

Methods
Studies were included in this analysis if they met the following criteria: original studies of patients with primary brain tumors and bone cancers, malignant mesothelioma, or non-Hodgkin’s lymphoma; the investigation of SV40 was performed on primary cancer specimens; the analysis included a control group; and the same technique was used for cases and controls. Included reports were published from 1975 to 2002.

Results
Thirteen studies fulfilled the criteria for the investigation of primary brain cancers (661 tumors and 482 control samples). Specimens from patients with brain tumors were almost four times more likely to have evidence of SV40 infection than were those from controls (odds ratio [OR] = 3.9; 95% confidence interval [CI]: 2.6 to 5.8). The association was even stronger for mesothelioma (OR = 17; 95% CI: 10 to 28; based on 15 studies with 528 mesothelioma samples and 468 control samples) and for bone cancer (OR = 25; 95% CI: 6.8 to 88; based on four studies with 303 cancers and 121 control samples). SV40 DNA was also more frequent in samples from patients with non-Hodgkin’s lymphoma (OR = 5.4; 95% CI: 3.1 to 9.3; based on three studies with 301 cases and 578 control samples) than from controls.

Conclusion
These results establish that SV40 is associated significantly with brain tumors, bone cancers, malignant mesothelioma, and non-Hodgkin’s lymphoma. Studies are needed to assess current prevalence of SV40 infections.

http://dx.doi.org/10.1016/S0002-9343(03)00087-1