The application of the Keshe Foundation GANS Plasma Technology to prevent and overcome the African Swine Fever and the blue ear disease the large-scale farm trial in China

From Keshe Foundation Wiki
Jump to: navigation, search

This article is part of the KF Plasma Times April 2019

Kfplasmatimes10 african swine fever.jpg
Test site:Pig farm with a building holding 829 pigs, aged 50-days-old, with average weight of 25kg.

Test carried out by the request of the Chinese government officials with Keshe Foundation providing the

material and farmers applying the plasma technology.

Collaboration: Keshe Foundation scientist, the management of the farm, their specialists, farm workers

and the renowned Chinese professor supervising the process in live animal husbandry.

The pig farming company owning and operating multiple farms with 2 million pigs in China.

Test date: 19th January 2019 to 3th February 2019

TEST BACKGROUND

The success of the first two trials of treating the African swine fever by Keshe Foundation, has attracted the attention of relevant department in pig farming sector in China.

1.1. FIRST TRIAL

In the first trial carried out by the Keshe Foundation, the GANS plasma technology was applied on a pig which for 3 months was suffering from the ASF. In this case the farmer was supplied with the GANS plasma water and applied it accordingly to the received instructions. Within 3 days, the first signs of recovery were observed and within 7 days, the pig did not show any signs of the fever and entered full recovered (full case documented in Appendix A).

1.2 SECOND TRIAL

The second trial demonstrated the successful reversal and prevention in pigs infected by the ASF, treated within the first two days of detecting the condition. When the symptoms of vomiting and lack of appe- tite were first discovered by the farmer in his small 30 pigs’ farm, the GANS plasma technology was immediately administrated by him. The farm was located in the highly infected ASF area and the farmer is one of the knowledge seekers, following the Keshe Foundation. He contacted the Foundation and requested help, and so the GANS materials were immediately delivered to him. The pig farm and all the pigs were immediately sprayed and watered, by the farmer, with the revolutionary GANS plasma water. The farmer immediately noticed the stoppage of the spreading of the virus to the rest of his pigs and after two weeks of not observing any symptoms of the virus, he manage to sell his pigs on the market (full case documented in Appendix B).

1.3 THIRD TRIAL

Following the success of the first and the second trial, the Keshe Foundation keept the Chinese government officials informed and aware of their achievements and requested for a larger test trial, this time to be observed and controlled by independent observers and officials. In mid-January, the Keshe Foundation was notified by the leading professor appointed by government, to be ready for an 80-pigs test trial. In response, the Foundation prepared materials ready for this trial case.

A meeting with industry experts was arranged by the National Security Department. After explaining in detail, the principle of plasma technology to eliminate viruses and the process of applying the plasma technology, the professor arranged for the Keshe Foundation to visit a farm, belonging to a large pig company in China, which was infected by the ASF virus. The professor and the CEO of the company in writing confirmed to the Keshe Foundation that in one of their farms, a number of pigs were tested positive for the ASF. The professor and the government officials requested the Keshe Foundation to undertake a larger than originally plannedA meeti trial, involving 829 animals. The Keshe Foundation representative, together with the afore-mentioned professor, the CEO, the general manager and the team of technicians and farmers, attended the infected farm on Saturday, 19th January 2019. This farming company, in 2018 bred and sold more than 2 million pigs. The professor informed the Keshe Foundation officials that the company lost thousands of pigs in the past months since the out-break of the virus in China, which has had a serious impact on the company's business.

On attending the farm by the Keshe Foundation and the management of the company, the process of reversal and prevention was immediately implemented. It was then left to the management, the workers and the technicians of the company to observe and document the outcomes of the initiated process. The Keshe Foundation visited the farm the following Saturday and the company was happy with the outcomes.

After 14 days of the start of the trial, the Keshe Foundation and the management of the company met on the 28th January, in the presence of the Chairman, at the headquarter of the company. Based on the success of the initial trials, the company requested from the Keshe Foundation to provide materials, for the prevention of the ASFV and the Blue ear virus, for one of their mother pig farms, where they had positively identified the ASF virus. The GANS water material for this purpose was delivered to the company on February 3rd and was applied on the cohort of 1000 pregnant pigs. At the time of compiling this report (13th February), the Keshe Foundation has not received any reports from the company on any losses or cases of infection on the farm.

VIRUSES

2.1 AFRICAN S WINE F EVER VIRUS

African swine fever virus is a large enveloped double stranded DNA virus that is the sole member of the genus Asfivirus within the family Asfarviridae (Asfar = African swine fever and related viruses). African swine fever virus is the only known DNA arbovirus and is transmitted by soft ticks of the genus Ornithodoros. Virus strains are distinguished by their virulence to swine, which ranges from highly lethal to subclinical infection. Virus strains can also be differentiated by their genetic sequences, and various virus-encoded genes, including P72 (also referred to as P73) that can be used for genotyping the virus; however, the genomic diversity of the virus in the nature, remains to be thoroughly characterized. The genome of African swine fever virus contains a unique complement of multigene families.

2.2 PORCINE REPRODUCTIVE AND RESPIRATORY SYNDROME VIRUS

Porcine reproductive and respiratory syndrome (PRRS), also called Porcine Blue Ear disease, is a highly contagious disease caused by porcine reproductive and respiratory syndrome (PRRS) virus. Concomitant as lower reproductive, difficult breathing and blue or purple ear, and causing other infectious diseases are its main characteristics. Porcine blue ear disease virus is a single-stranded RNA virus, which lacks a corrective mechanism in the process of viral infection and replication and produces a high mutation rate of offspring virus. The mutation rate of PRRS is 1,000 times higher than that of other DNA viruses, 1 million times faster than the mammalian genome.

INTRODUCTION M.T. K ESHE OF THE NEW SCIENCE AND TECHNOLOGY BY NUCLEAR SCIENTIST

A new discovery and understanding

The new GANS plasma technology of the Keshe Foundation was developed for deep space virus applications and as reported on in this document, successfully resolves the AFS and PRRS virus cases.

In collaboration between the Keshe Foundation’s and the South Sierra Leone University’s scientists, through testing and confirmation of the effectiveness of plasma technology in Ebola virus trials in Africa, it has become clear that the new space plasma technology is very effective when dealing with viruses.

Up to now, the world of science had problems in understanding the operation, working and effects of viruses on human and animal cells. Modern medicine developed antibiotics to deal with the infected cells, but we never fully understood the working of cells which are infected by a virus. Plasma science educates us that we have to look at viruses as energy packages which link and attach themselves to organic cells and until all the energy of this energy pack is used, the signs of the virus will be present in that cell in the human or animal body.

The new space technology by the Keshe Foundation, through the application of plasma energy packs produced by the GANS material, has the ability to deplete the energy of the virus that attached itself to the amino acid or to the cell, by creating a condition that causes the virus to immediately disappear from the affected cell.

Where, the energy of the virus is now in much weaker strength is delivery to the GANS plasma which does not bear any strength of the original virus. Where the virus energy is broken up into a weaker field in the GANS plasma.

With this depletion of the energy from the virus, the virus lives behind damage cells which can lead to secondary infections and at the same time, due to the depletion of the stronger strand of the virus, the energy which remains in some cells, behaves and becomes the second weaker virus in the energy magnetic field strength, which affects the RNA of the animals. The weak strand RNA, now manifest itself in some of the weak cells or new cells as an RNA virus, known as Blue ear. The new RNA strand of virus now creates a secondary virus known as Blue ear virus. Then the new strand of virus, attaches itself to new cells and leads to a creation and observation of high temperature and fever, after the first temperature caused by the African swine fever virus.

Continuous application of a new GANS plasma technology with the weaker strength GANS water to match the strength of the Blue ear fever to be fed for the second time to the animals to deplete the energy of the new virus involving to new Blue ear virus and totally eradicate the new virus.

As in the case of the African swine fever, this new eradicated secondary virus leaves some damaged cells in the body of the animal, which these damaged cells lead to the manifestation of secondary infection, as in the same as with African Swine fever, which these new damaged cells leads to manifestation of second cycle of high temperature in the body of the animal.

Therefore, M.T. Keshe uses a third new GANS plasma strength material in the strength of the antibiotic. This third GANS by test in laboratories in Europe supports that this GANS is many times more powerful than any antibiotic, in giving to the animals during the two infections period of the African swine fever and to Blue ear fever in the body of animals will reduce and eliminate the fever.

M.T. Keshe has suggested and showed in the 829 pigs’ trial that the introduction of the GANS plasma water to the environment of the whole pig farm building, immediately converts the African swine fever and consequently the manifestation of the Blue ear virus. Usage of the plasma water for infection control in one of the trial groups, overcame the virus and its infection.

The company was advised to provide amoxicillin in the section three and four and that in 7 days, saved the life of all the infected animals in the control groups in the building.

Within 14 days of application there is no sign of the virus or fever in any of the infected animals in the farm house. Prior to the application of the plasma technology, all the animals were showing the symptoms of high temperature and fever.

This is a major breakthrough in the world of science and from this point onwards makes it possible to handle and overcome any viruses infecting animals or humans. The solution is to find the strength of the virus and simply develop a weaker strand of the same strength. So that, as the virus delivers its energy to new GANS plasma water it losses its strength/energy and leaves no signs of the virus. This is a major breakthrough in the world of science and a new understanding of the work of viruses in the space which now is unraveled by the Iranian nuclear physics, expert in the Space plasma technology. The development and application of the new plasma material known as Gas in Nano-state Solid (GANS) was successfully tested in a number of trials in China in the areas of agriculture thus increasing the harvest, and in medical applications of the technology through European-certified health systems.

Notes: It has to be understood, in the GANS plasma technology, the high strength energy magnetic gravitational fields always feed the lower strength magnetic fields of the same, to bring the interaction of the two into balance. Therefore, large amount of same strength always feeds its energy to the lower amount of the same strength. Therefore, in viruses, the virus energy pack has to find a matching field in the amino acid spectrum strength to be able to interact and lock into one of the elements of the amino acid. (O or H, N and C). Understanding that all the elements of the amino acid of every cell are not of the same strength explains why the viruses can attach themselves to different animals or humans and only affect certain animals or species and cannot cross to other animals.

The second aspect which can now be answered is that now that the higher strength of the virus strand is consumed, the weaker strand attaches itself through the RNA strength, to the stronger element of the amino acid of the protein. In that process, as it is closer to the stronger element of the protein, the exchange of the energy of the virus to the protein is less and so this leads to a weaker and less damage to the cells of the body of the animal. Therefore, the animal can live longer life, but still shows the effect of the same virus or the mutation of it, if the strength of the weaker strand of the virus is at the same strength of the RNA as that of the weaker DNA strenghth. Therefore, the weaker strand RNA energy strength in having the matching strength to the heavier element of the protein, now locks into the animal cell as a weaker strand of the same virus, or similar to another virus strand strength can manifest itself and a totally new virus can be observed.

It has to be understood that in plasma technology when we use the term ‘GANS plasma water’, this water is not plain water, but it carries plasmatic magnetic fields potential. This means that when we use GANS Plasma water as feeding water or spraying water, it affects the entire environment even several meters around the application area by covering it with the magnetic fields of plasma, and not only the area that is in direct contact with it. The GANS plasma water makes a magnetic, energetic field connection with the surrounding environment and can cover the whole area and not only the area which is watered with it.

Therefore, when we spray or feed the animals, the field of the GANS plasma water spans across the whole body of the animal, without going through the blood or lymph circulation. Therefore the interaction in the body of the animal or in the environment treated with the GANS plasma water is instantaneous. As a result, the effect of the plasma water in the given environment, can last for weeks and months.

TRIAL PROCESS

COMMUNICATION WITH THE PIG FARM TO PREPARE THE PROCESS

Fig. 1. Conversations for preparing the trial.

On January 17th, 2019, the Keshe Foundation received confirmation that a pig farm infected with the ASFV was found for testing. The initial communication with the Keshe Foundation was to prepare the farm to receive and apply the new material. The instruction was given for the farm to prepare a number of 50-liter plastic buckets, each with a tap positioned at one third height from the bottom of the bucket (Fig 1. - A).

Conversation’s translation (Fig 1. – A): A:

Good morning, Director Zhou told me that on Saturday, we will go with you to the farm. Can I know the details of the arrangement? Mr. Keshe wants to stay there for couple of days to see the preliminary test results. A: We need the farm to prepare four, 50-liter buckets as showed in the picture above, the tap should be positioned one-third from the bottom of the bucket.

A: We need four groups of pigs to do the test, keep the sick ones in the old environment, we need to deal with the environment.

Additional information

In addition to the process and treating the infected pigs, we suggested that the farm can sterilize the flesh of sick and dead pigs with the GANS water to test if it eliminates the virus from the flesh of the ani- mal, which can prevent the infected meat from entering the food chain (Fig 1. – B).

Conversation translation (Fig 1. – B):

A: Is it possible to prepare some flesh from the dead pigs, when we arrive there on Saturday? We want to test if the virus in the meat can be killed by just treated it with GANS water.

B: Sick pigs need to be buried to follow the regulation.

A: He just wants to test before you bury them. He promises that he will not eat it.

A: This is important for the security of the food chain.

UNDERSTANDING THE SITUATION THE A FRICAN SWINE FEVER VIRUS OF PIG FARMS AND CONFIRMING THE PRESENCE OF

Fig. 2. Confirming the ASFV was detected in the target farm

On January 18th, 2019, the basic information on the pig farm was provided to the Keshe Foundation and the professor appointed by the government and General Manager of the company, confirmed that the ASFV laboratory blood test was positive.

Before the onset of the virus, it was confirmed that there were 829 piglets in the farm building. These pigs were around 50-days-old and weighed, on average, around 25 kg. By January 18th, there were about 810 piglets left, as 19 pigs already died in the first 24 hours.

Clinical symptoms began to appear in the farm building on January 16th, and blood samples of 10 pigs were tested in laboratory on January 17th. The results confirmed the presence of the African swine fever virus.

From January 17th, pigs in the farm began to die: 7 pigs died on January 17th, 10 died on January 18th and 19 died on January 19th, before the Keshe Foundation team arrived at the pig house, at 2PM.

Conversation’s translation (Fig. 2):

A: Were those pigs checked for the virus before our trial?

B: Let me check.

B: Already confirmed by laboratory means.

A: May I ask how many pigs were there to test?

C: Total 810, sampled test, so it is not exactly certain which pig were sick.

C: They are piglets, about 50-days-old, weighing around 25kg.

C: There is a building nearby, which also has more than 800 pigs, around 130-days-old, not showing sickness yet. This building needs prevention, very close, just 8 meters away.

C: No, they showed clinical symptoms the day before yesterday, and hence sent the samples to the laboratory to test, the result shows ASFV positive.

B: Should we focused on prevention tomorrow?

C: The process is human isolation, pig pens isolation, and environment disinfection.

I think these 800 pigs to do the process, and the other 800 is to do the prevention.

I MPLEMENTATION PROCESS AND TRACKING FEEDBACK

Kfplasmatimes10 africanswinefever figA-B.png

DAY 1

On site

The Keshe Foundation officials were picked up by the professor and driven three hours to the city nearby the farm. At arrival, introducing the CEO and the General manager and the local stuff of the company.

Mr. Keshe, the founder of the Keshe Foundation arrived at the hotel at 10:30 on January 19th, where he had a meeting with the managers and staff of the pig farm company to understand their situation and he explained the application scheme and principles of the new GANS plasma technology.

Arriving at the pig farm around 1pm, we observed that one or two pigs were dead in each pen due to the virus and some of them had not been moved out of the pen (as can be seen in some of the pictures below). The Keshe Foundation team immediately took videos and notes of the sick pigs.

Most of the pigs were inactive, we could observe the high temperature from the color from the skin (Bright red color as was pointed out by the staff of the company due to fever). Most of the pigs were huddled together, some pens had the traces of vomit on the ground, and the excrement of the pigs was inside the pens. The smell of the place was so bad that we felt uncomfortable in the throat and lungs after a while, one could smell the death in the farm house. Some pigs were very thin and sick.

In the last picture (Fig 3. – J) on the right, one can see the dead animals were placed in bags for disposal.

Start of on-site process to reverse the virus
Kfplasmatimes10 africanswinefever fig4.png

Due to the limited raw materials brought in by the Keshe Foundation - as the original plan by the profes- sor was to process 80 pigs at a different site - we had to improvise to cover as many pigs as we could and at the same time create separate application and control for maximum coverage of the whole pig house of 810 pigs.

Therefore Mr. Keshe decide to divide the whole pigsty into five sections and apply different process to each section.

As in Fig. 4, from the entrance, the furthest 6 pens including both left side and right side, that is pens No.17 to No.22, were labeled as Section 1. The following 6 pens, that is No.14, No.15, No.16, No.23, No.24 and No.25 were assigned to Section 2. The next 6 pens, including No.11, No.12, No.13, No.26, No.27 and No.28 pens, were marked as Section 3. Pen No.3 to No.10 and No.29 to No.36 constituted Section 4. The first pen on the right side of the entrance - pen No.37 - was designated as the sick bay, where all the sick animals from all the pens were isolated before dying. Pen No.2 was designated as the dead animals’ storage, with animals temporarily packed in plastic bags.

Kfplasmatimes10 africanswinefever fig3.png
Fig 4. Division of pens into the five sections.
Sections 1 to Section 4, were isolated from each other by placing a large plastic sheet across the building (as depicted in Fig 5. – A).
Fig 5 - A + B
Fig 5 - C + D
Section 1 was then cleaned of any animal waste (Fig 5. – B) and then sprayed with the specific GANS water mixture, labeled as W (collected from the top of the plastic container) with the animals inside. The entire surface of the bodies of the animals located in this section were sprayed with the ‘W plasma water’ (Fig 5. – C).

At the same time, the dead pigs and those with severe symptoms were removed. The body temperature of random pigs was measured (Fig 6. – A), and the pigs which body temperature was tested were marked (Fig 5. – B).

Fig 6. Measuring the body temperature of pigs, on January 19th, 2019.

There were 24 pigs in pen No.17, 2 pigs were seriously sick and hence were moved out, with 22 pigs left. The body temperature of the four chosen pigs was 40.5, 40.4, 39.6 and 39.7 degrees Celsius, respectively (Fig 7 – C).

Pen No.18, originally had 26 pigs, with one removed due to sickness, leaving it with 25 pigs. The body temperature of the two randomly selected pigs was 41 and 40 degrees Celsius, respectively (Fig 7. – B).

Pen No.19, had 3 dead pigs and one with a fractured leg, so there were 22 pigs left in total in this section. The body temperature of the two selected pigs was 40.3 and 39.9 degrees Celsius, respectively (Fig 7. – A).

Pen No.20, originally had 23 pigs, one dead animal was removed and there were 22 left. The body temperature of the five randomly selected pigs was 41, 40.5, 40.4, 40.2 and 39.7 degrees Celsius, respectively (Fig 7. – D).

Pen No.21, originally had 25 pigs, no pigs removed. The body temperature of the four selected pigs was 41, 40.4, 39.5 and 39.2 degrees Celsius respectively (Fig 7. – E).

Pen No.22, originally had 23 pigs, there were 22 left after the removal of one seriously sick pig. The body temperature of the three chosen pigs was 41.8, 40.2 and 39.9 degrees Celsius, respectively (Fig 7. – F).

The number of pigs in these 6 pens totaled to 145 prior to the removal of diseased and dead pigs, which left 139 pigs at the start of the trial in this section (Fig 7. – A).

The normal body temperature of a healthy pig is below 39.5, and hence most of the measured pigs showed first signs of fever.

After taking body temperature measurements, both the pigsty and the pig were sprayed, and pigs were fed with GANS water. The blood samples were collected after one hour from the first feeding of pigs with GANS water.

From pen No.17, blood sample of one of the pigs was collected and the test tube number is 674-1-1. The same was done for pen No.18 and the test tube number is 939-2-1. Sample from a pig in pen No.19 has the test tube number 855-1-1.

From pen No.20, two pigs’ blood samples were collected, and each sample was divided into two parts. For pig No. 1, one blood sample was labeled as 900-4-1, the other sample had ‘F1 GANS’ water added to it to test the effect of the GANS water on blood (sample labeled as 932-4-1-F1). For pig No.2, one blood sample was labeled as 940-4-2, to the other one ‘W GANS’ water was added to test the effect of the GANS plasma water on blood. The second test tube number was labeled as 879-4-2-W.

In the pen No.20, one of the pig’s blood was collected, the test tube number is 912-5-1.

From pen No. 22, one pig’s blood sample was collected, and it was divided into two parts. One sample was labeled 953-6-1, the other had ‘F2 GANS’ water added to test the effect of the GANS water on blood. The second test tube was label as 612-6-1-F2.

Control group blood samples were bundled together, and on the same night, 10 blood samples were placed in a paper box and sent to the laboratory for testing.

As it was explained in the introduction to the GANS plasma technology, it should now be understood that the GANS waters added to a number of blood samples sent to the laboratory for testing for the presence of the virus; the plasmatic fields in these test tubes affects all the blood samples and negative results were expected for the presence of ASF and PRRS viruses.

Kfplasmatimes10 africanswinefever fig6b.png
Fig 7. Original record of pig numbers, temperature measurement and blood samples from the six pens of section one.
On the night, after spraying and feeding pigs with GANS water, the piglets quietly laid down togethern (Fig 8. – A, B).
Fig 8. Piglets laid down quietly after GANS water feeding.

All the sick pigs from the other untreated areas were moved to the pen No. 37 by the entrance and were sprayed and fed with the ‘W GANS water’ only.

At this point, the full length of the central corridor was sprayed with the ‘W GANS water’ twice to change the whole environment of the building.

For the frequent use of the GANS water in tanks, the GANS water needs to remain still for 6 hours for the GANS to settle at the bottoms of the tank. Then the energized water, which gained the magnetic and gravitational field strength of the GANS, is ready to be used for the next batch of feeding and spraying of the farm building.

Due to the large number of animals that escalated from 80 to more than 800, the GANS plasma water production could not fully meet the demand of the pig farm. Therefore, the original water feeding system of the pig farm was turned on after one night, and the pigs drank both, the normal water from the pipes and the GANS water. Therefore, the lack of availability of sufficient amounts of GANS water to feed the animals with, has extended the process by couple of days.

On January 19th, The record was written for the comparation the food consumption in the future that all pigs were fed with 14 packs of food and the Section 1 consumed only 3 packs of food.

DAY 2

On site

At 1pm on January 20th, 2019 the status of the pigs was assessed. Piglets were still dying in untreated areas, but the numbers were lower than in the previous day (Fig 9 – A, B).

The treated pigs in Section 1 were active during the GANS water feeding (Fig 10. – A). The piglets laid still together after drinking the GANS water (Fig 10. – B).

Fig 9. Pigs which died on January 20 th , 2019.
Fig 10. Piglets drank and then lied down after drinking GANS water, on Jan 20th 2019.
Fig 11: The pigs in the sick pen, on January 20th 2019.

Pigs in the sick pen (pen No.37) were very weak and continuously dying.

The body temperature of the pigs on the farm, was continuous monitored during the trial.

In Pen No.17, one pig which was previously tested had a body temperature of 41 degrees Celsius.

In pen No.18, one pig which was previously tested had a temperature of 40.1 degrees Celsius and another randomly sampled pig had a body temperature of 39 degrees Celsius. Therefore, the first signs of the effectiveness of the GANS plasma water on animals started to show in the drop of the body temperatures to 39 degrees Celsius.

Fig 12: Conversation regarding retesting of the blood samples and keeping them separate

In pen no.22 one pig which was tested before, was measured to have a body temperature of 40 degrees Celsius.

One day since the start of the processing, most of the pigs remained feverish and were not yet showing any signs of recovery.

The test results of the first batch for all 10 blood samples collected on the 19th was reported by phone from the laboratory in the afternoon of January 20th. We were told that for all the samples the African swine fever virus was negative, but what was more peculiar was that the virus reference control samples in the laboratory, had also failed to detect African swine fever virus.

In response, Mr. Keshe explained (please read the note in the introduction of the new technology in respect to the influence of the fields of the GANS plasma water on its environment) that the GANS plasma depletes the energy of the virus through the interaction of the fields of the water and the virus to GANS plasma water. Therefore, the GANS water which was added into couple of the blood sample tubes has affected the virus present in all the 10 test tubes by neutralizing it. Therefore, in the laboratory tests not only the blood samples shipped to the laboratory showed no signs of the virus but al- so all the other samples brought together with them, were tested as negative due to the GANS plasma water depleting the virus in all the samples.

The same result was observed in the agriculture section of the application of GANS water, where the seeds watered with the GANS water and the neighboring seeds that were only watered with standard water, grow at the same rate. Only the referenced sample that was 100 meters away, has shown far lower growth than the GANS-watered section. Therefore, the GANS water affects the entire environment of the virus, and not only where it comes in direct contact with it. 

Therefore, it is advisable that the subsequent samples for the control group, are kept at all time at a distance of more than one meter apart from the samples from the treatment group or those that have GANS water added directly to them (Fig 12).

Conversation’s translation (Fig. 12):

A: Mr. Keshe suggest that you keep those 10 blood samples and also the control blood and try to get a new control blood sample. If you can test positive for the new control blood samples, and those other 10 samples still keep negative, then this can also explain how the plasma field changed the blood samples.

A: Your laboratory should strictly separate any blood samples processed by our technology, the needles needs to be separated and need to separate the samples during the transportation by a minimum distance of one meter. A: Take blood samples every day, at the same time, so it is the time to take blood test this afternoon again.

B: Already arranged to take blood samples again this afternoon. Thank you.

The Keshe Foundation team left the farm at 3pm on January 20th, 2019. It was requested by Mr. Keshe to carry on with the processing of the 6 pens in Section 1, and of those pigs in the sick pen – to spray the ‘W GANS water’ on the pigsty, corridors and the body of pigs, three times a day; also to feed the pigs in Section 1 with ‘F1 GANS water‘, three times a day and to fed pigs in the sick bay with the ‘W GANS water' all the times.

On the evening of January 20th, 2019, a weak pig was reported dead in Pen No.17. The dead body was sent to the laboratory to check for the presence of African swine fever virus and for the first time the laboratory confirmed the presence of the Blue ear disease as the cause of death. This confirmed Mr. Keshe’s theory of a change of a double strand DNA virus to a single strand RNA virus, where previously there were no signs and no confirmation by the farm or the laboratory of any Blue ear virus case.

On January 20th, 2019, blood was collected again from pigs in the first test section.

Fig 13. One pig died in pen No.17, on January 20 th , 2019.

DAY 3

Fig 14. Empty disinfected Section 2.

On January 21st, Mr. Keshe on return to Beijing, asked for an implementation of a buffer section between Section 1 and the other pigs, which were not processed.

Therefore, the farming team moved out all the pigs in the 6 pens next to Section 1, to Section 4, this included pen No.14, No.15, No.16, No.23, No.24 and No.25. The floor and the ceiling of these pens, marked as Section 2 in Fig. 4, were cleaned with normal water and then sprayed with ‘W GANS water’, and also separated from Section 3 with plastic sheets for total isolation.

Because the hog house is a large open space, even though isolated with plastic film, there is no way to completely seal sections of it, as some air can still float between. The personnel multiple times a day walks through all the areas using the central corridor and hence walks between the infected pig pens and the test trial area. Therefore, a buffer section was established to reduce the possibility of transportation of the viruses from one section to the other. Section 2 is sprayed once a day with ‘W GANS water’ for disinfection and protection.

Every day the central corridor was sprayed three times a day, with ‘W GANS water’.

The instruction was given by Mr. Keshe to create a third section to test the effect of the different GANS strength on pigs. The farming team separated six more pens adjacent to the Section 2 and isolated them with plastic sheets. This section covers pen No.11, No.12, No.13, No.26, No.27, and No.28 and was marked as Section 3 of the trial area (Fig 15 – A, B).

In this section, the procedure was slight different and involved spraying the pens once a day with the ‘W GANS water‘ to neutralize the field of the viruses, and at the same time once a day spraying of the pigs’ body and feeding them with the ‘W GANS water’ (Fig 15 – A, B).

The total numbers of pigs in this section at the outset of the segregation was 131 pigs, after moving all the sick pigs out into the sick pen and washing the pigs and the pens with the ‘W GANS plasma water’.

The breakdown of the number of pigs in each pen was as followed: 18 pigs in pen No.11, 23 pigs in pen No.12, 21 pigs in pen No.13, 25 pigs in pen No.26, 22 pigs in pen No.27, and 22 pigs in pen No.28.

Fig 15: Instructions of procedures for Sections 2 and 3.

Conversation’s translation (Fig. 15):

A: Tomorrow, please move out the pigs in the 6 pig pens of the third section , and use our ‘W GANS water’ to disinfect it, and choose 60 to 70 pigs in good condition, send them back to 3 of the 6 pens, keeping 3 pens toward the entrance empty. Spray the pig pens in Section 2 and Section 3 once a day with ‘W GANS water’ and spray the body of pigs in Section 3 also once a day. Also feed the pigs in Section 3 with the ‘W water’. Please notice it is the ‘W water’ and one needs to hold the water still for 6 hours, until it has no floating blue particles, and only then can use the water to feed the pigs. You can move one bucket from Section 1 to Section 3.

A: Keep spraying the pens and pigs and feed the pigs in Section 1, three times per day before Wednesday.

A: Everyday, check if the temperature of the pigs dropped.

A: If any pig dies in the test area, please take pictures.

A: Now the second isolation section is empty. Is the third section cleaned and disinfected and the healthy pig put back?

A: Pay attention to the top of the plastic film where the air can come in, spray more times, and all the ventilation openings also need to be sprayed every day.

B: The third isolation section, we are still working on it, but those pigs in Section 3 have nowhere to go, because the pigs in Section 2 are already moved to Section 4. If we move all the pigs from Section 3, it is too much, cannot put into.

B: Can we move all the sick and week pigs from Section 3 to Section 4?

A: Yes, but the floor needs to be washed with water, then pick out all the sick and weak pigs in Section 3 and move to the sick pen and send those healthy pigs back into Section 3 after disinfection. Do not put any pigs in Section 2 now.

The remaining pig pens, pigs of which were not given or sprayed with any GANS water, were called Section 4. The only process of keeping the spreading of the virus under control was spraying of the central corridor area with the ‘W GANS plasma water’. This proves that a change to the environment can prevent the pigs from getting infected, only by breathing and being in the environment of the fields.

On 21st Jan, the lab test result of the blood samples from the feverish pigs’, taken on January 20th, showed negative results for African swine fever virus (Fig. 16 and Fig. 17). The pathological test result for the pig that died in pen No.17 on the 19th of January, also gave negative for the African swine fever virus.

Fig 16. Confirming the blood test result is ASFV negative.

May I know the test result of blood?

Please share the test result in time after it comes out, as a reference to adjustment of the test process.

The test result is negative, but we are not sure if those pigs were infected originally.