0418-2017-Cancer in Exchange for Peace

https://www.youtube.com/watch?v=vbRZli-XM48

Introduction:
The Keshe Foundation (KF), an independent, non-profit, non-religious,
space-based organization founded by nuclear engineer, Mehran Tavakoli
Keshe, is introducing to humanity, the science of the universe, plasma
science. KF develops universal knowledge in space technology to provide
solutions to major global problems revolutionizing agriculture, health,
energy, transportation, materials and more. The application of plasma
science in the form of specially developed plasma reactors and devices will
give humanity the real freedom to travel in deep space. Plasma science
exists throughout the whole universe. It is here and it belongs to you. Our
knowledge, research and development regarding the plasma structure has
progressed to the point of enabling everyone to participate in the process.
Become a creator and understand the work of the universe for the good of
humankind on this planet as well as in space.
www.KesheFoundation.org
Plasma, GANS and Nano Materials
The use of Magravs, Nano materials, GANS, liquid plasma, field plasma and
other plasma technology have come as a new dawn for humanity to progress
and work in harmony with the universe. Conventional technology
applications are wasteful, damaging and cause pollution to the planet and
all living beings. Plasma science offers solutions and improves existing
methods and use of resources in all aspects that touch the lives of all beings.
Plasma is defined by the Foundation as the entire content fields which
accumulate and create matter and is not defined by physical characteristics
like ionization or temperature. Also with plasma science we understand how
we can convert matter back to the fields. According to Mr. Keshe Magrav
stands for magnetic gravitational which means that plasma absorbs or
gives. And every plasma has both; it has give and it has take and when they
cant find the balance they distance themselves until they find balance they
can give to the others, that they can receive what they want to receive and
give further. Certain atoms and molecules release and absorb magnetical
gravitational fields. Released fields are available to be absorbed by other
objects.
The KF has developed a way to gather these free flowing fields from
the environment within a resourceful and beneficial new state of transitional
matter which M T Keshe named GANS. The first step of the process of the
formation of various basic types of GANS is nano coating metal. This is

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carried out by either chemically etching steam coating with sodium
hydroxide or thermally by heating by fire coating by gas burner. During
either coating processing gaps between the outermost layers of atoms are
created. The residual coating is often referred to as nano coating defined by
the structured layers of nano material which build up during the creation
process of the coating. Nano coated metal in interaction with various metal
plates in a salt water solution creates Magrav fields. These fields then
attract available elements to form a specific gans which collects and settles
at the bottom of the container. This GANS is formed from independent
energized molecules like little suns that can be used in various applications.

03:50
The KF is extending invitations to medical doctors of any practice and
specialty to apply to the foundations private weekly medical workshop.
This includes medical doctors, dentists and veterinarians. Scientists of the
KF develop different types of plasma therapies and cures that utilize
advanced, non-invasive plasma technology. The weekly, private medical
teaching workshop educates doctors to the plasma science behind the
therapies along with the functionality and operation of revolutionary plasma
medical devices. The goal of the private teachings is to add plasma health
knowledge to the profound knowledge of medical doctors. The weekly class
is broadcast live over the internet through a secure, private channel every
Wednesday from 2 to 5 pm Central European Time. Presently, the class is
only offered in English. However you are free to bring a translator to the
class. If you cannot participate in the live broadcast you can watch them
later at your convenience through a private internet portal. Every patients
case that is discussed in the workshop will be kept anonymous and private.
This includes catalogued findings and data gained from the analysis of the
patients health issues.
Any medical doctor in the world who wants to participate can do so
by sending an email to doctors@spaceshipinstitute.org . In your email
please state your willingness to participate in the medical teaching
workshop. If you are planning on bringing a translator to the workshop,
please state this in your email as well. After we receive your email we will
contact you with the instructions on how to apply to the workshop. As a part
of the application process, applicants who apply including any translators
brought into the workshop will be required to sign the KF World Peace
Treaty which can be found at the following we address:
http://keshefoundation.org/worldpeacetreaty/WorldPeaceTreaty.pdf

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All applicants will be required to provide proof of their education and
ability to practice medicine and will also be required to pass an extensive
security background check before they are granted access to the teaching
workshop. Healthful plasma technology is here now, the use of which
increases exponentially on a day to day basis on every continent. We
encourage you to come and learn about this revolutionary technology. Apply
today.

The KF is extending an invitation to experienced farmers, agricultural

specialists and researchers to apply to the foundations private weekly
agriculture teaching workshops. If you fall into one of these categories and
are interested in plasma technology integration into agriculture you are
invited to apply. Scientists and agricultural technicians at the KF
continually develop and apply new methods of food and fiber production,
soil fertility management, plant and livestock health management and
increased farm production using the most advanced plasma technology that
is taught at the KF spaceship institute.
In the teaching workshop you will learn the science of plasma
technology and its application in the field of agriculture for enhanced and
equitable global food production while minimizing costs and external inputs.
Practicing farmers and KF scientists will demonstrate their application of
plasma technology in agriculture and the ensuing results of such
applications thus deepening and enriching learning for all participants in
the private teachings.
Participants are encouraged to demonstrate their farming practices in
the teaching workshop. The private teachings are broadcast in English live
over the internet through a secure private channel every Wednesday at 10
am to 1 pm Central European Time. If necessary you may bring a translator
to the workshop. All applicants are required to provide proof of their
education and professional qualifications and must pass a security
background check and are required to sign the Keshe Foundation World
Peace Treat which can be found at the following website:
http://keshefoundation.org/worldpeacetreaty/WorldPeaceTreaty.pdf
Translators that attend must also pass a security check and sign the World
Peace Treaty. For details on how to join the private teachings in agriculture
send and email to
agriculture@kfssi.org stating that you would like to participate. Include in
your email your education and agricultural experience and the reasons for
your interest in plasma technology. Applicants will be contacted with
further instructions and details in the application process.

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Introductory video.

Cancer Blueprint Day April 18, 2017

11:02 Rick:
Welcome everyone to the cancer blueprint day of the Keshe Foundation
(KF) Spaceship Institute. This is the first of perhaps the weekly series that
may occur and it is Tuesday, April 18, 2017, and we have the title of the
workshop is
Cancer Solution in Exchange for PeaceCancer Blueprint Day
And this is about the new cancer solution breath-through being presented by
Mr. Keshe.

11:49: Mr. Keshe (K)

Good morning, good day to you as usual wherever and whenever you listen
to this group of teaching. As you remember we started the blueprint updates
2 years ago whenever we see a change of course. In that respect at this
moment we have come to the point that there is enough information,
knowledge, information, background knowledge and experiments done by
scientists on different aspects of the technology. We have to clarify the use
of the materials and how they have been used. This teaching today will
start a new course of action for the KF.

K: One of the biggest problems for humanity has been what we call cancer.
Cancer has been something that wherever and whenever the doctors could
not understand the knowledge of the change of the conditions of the
physicality of the body of the man. In that process when the doctors cannot
understand it they call it cancer. That is all it is. Now we started exploring
more and more and understanding more and more in how the cancer actually
progresseshow, where, why and which methods it is established in the
body of man. For the past 30 to 40 years to the knowledge of cancer has
become fairly tuned to full understanding. What we understand in KF is
very simple. Cancers are produced in 3 to 4 ways as far as we can see. One
is emotional and this is when thee emotion of the man creates a given energy
and that energy in interaction with the matter state of the body manifests
itself as an entity. In space we say that you can wish and you will receive.
You can put your hand out and have the energy from your soul that by the
filtering of your wishes of what the order is, you will receive the material.

14:17 K:

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We create the emotion of sorrow, we create the tears. We know the process
and we never knew actually how to control it. We create emotion of
rejection and in that process what we want to reject, we create the material
for it to start the process of rejection. In the olden stays man knew even how
to reject part of his arm, hand and fingers when they were trapped without
cutting it. The wish was so strong that like reptiles they could literally sever
the finger or the arms but this knowledge over time has disappeared in the
vocabulary in the knowledge of the man in the brain of the man. But to the
same extent when man wishes to create, to reject, to bring about a condition
where he wants to see a change and that change because it is given by the
wish of the man, it is so strong that no medicine can use radiation, you can
use anything you like in present medicine. But you will find out it will come
back again because in the world of medicine today, the world of science has
missed the main criteria of cancer. 95% of cancer is caused by emotion so
in that emotion and that condition man subconsciously wants to create a
condition in which that organ will not be there be it the prostate, the breast,
liver or the stomach cancer or whatever we might call it.

15:59 K:
We never understood and this is one of the main problems with the world of
science that cancer, the majority of it, is emotionally based and we wish it.
Our wish is so powerful that no medicine in the world can overcome it.
They give you chemotherapy, they give you everything else and after a few
years it comes back because in the present world of science the emotion of
the man is not calibrated. We have not considered it. With this new
technology where we tackle the source of cancer and that is why you see
such rapid changes and that is why we put this cancer teaching on. Now for
the first time we understand in the 99% of the cancer the physical change in
the structure of the body of the man is wished by the emotion of the man
through the source of the energy of the soul of the man. We wish it
subconsciously and we create it directly. Then we come to see what we
have created. It is very much as when we wish to have a longer finger for a
musician for an instrument in the same way we create these organs and these
materials inside ourselves.

17:40 K:
With the new technology which we offer and which is on the table that we
will discuss and see some facts of it and some papers which are delivered by
what we call the standard medical trial system. You see the explanation we
uses what we called certain gases in nano state of the matter we call gans

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where in fact no perfect system has ever been created to use and produce one
type of gans. In all the ganses produced especially with CO2 there is always
a minute amount of gans (gas in nano state) of zinc. That amount of zinc
within the structure of the CO2 plays its game. The emotion and neuro
system of the man work through the zinc in the gans state so why this
technology works well is because in one way you change the energy of the
tumor and on the other hand you elevate the soul of the patient through the
elevation of the emotion through the zinc. So this is what you see on the
results because now we understand it, we understand the process and the
situation and how it has risen.

19:09 K:
Why do you wish to have breast cancer? Why do wish not to have breast
cancer, but the wish for your child not to suffer the pain you suffered in
childhood? Or the wish that the child does not go through childhood that
you dont want the suffering to carry on was the best way. A woman gives
life through the breast for feeding the child. So we see the cancer in the
breast. We see the same thing when there is conflict between the father and
son and the majority of the time we see there is prostate cancer. Where does
the father give life to a child? The prostate is a player in the game. He wants
to get rid of what caused him the problem that he will never make the same
problem again.

19:49 K:
Now we understand that a lot of diseases are what we know as
psychosomatic which means psychologically through emotion we create the
physicality of the disease. Cancer is another one and more we understand
the more we realize the psychosomatic condition of cancer can be changed
in two ways. We can hammer it and bombard with radiation and
chemotherapy and anything else, or we can go a new way which is to solve
the problem at its root which is the emotion. Once you solve the problem at
its root you elevate the emotion so that with it you allow different fields to
reach or to be reached by the physicality the cancer is just a technicality to
change. This is important for us. This is why in the program today and in
the coming weeks you will see strange phenomenon and you will see things
that are impossible in the present world of medicine today. This is the
reason; for the first time we go to the essence of the majority of the cancer
positions which means the body want to produce something new so that the
mistakes of the past can not be repeated. In that producing the material is
accumulated and in that process creates cancer.

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21:30 K:
Cancers are literally done in a very simple way. What we see is very simple:
The body of the man has the emotion and in achieving that emotion it
creates a field and in the interaction where the field is received with that
emotion leads to the point of new tangibility of the matter.

The body of the man has a given content. It has copper, zinc, calcium,
potassium, and every other material which the body of the man carries. So
when the strength of the emotion filtered from the soul of the man in coming
to the matter solidifies to the center of the cancer. What we see, and Dr.
Rodrigo and other doctors will tell you this, is that up to now when you go
to the doctors, the doctors have not been concerned about what elements are
elevated in the blood. But in the new technology we have to because now
we understand if the strength of the field which is filtered from the soul of
the man through the emotion of the man comes to be at the strength of zinc
or copper that material in that point becomes the seed of the oyster of the
cancer. So every cancer has a center and in that process once it is started the
immune system of the body of the man tries to get rid of what is created by
the emotion and by physicality. So now we get what you call an immune
system attack trying to disturb or destroy the center, the material that the
emotion of the man has created.

24:09 K:
In that process what see as it carries on is the furtherist one comes into play
and now we see the oystering. And we see the growth of the tumor. And if
this condition is repeated because now that you have managed to survive it
gets replicated in other parts of the body of the man.

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So in this technology we can deplete the oyster and then remove the wish of
the man, the center element. Or by looking at the blood results in the
element sector we see what material is elevated and that material which is
elevated gives you the indication of what makes the seed of the cancer cell.
In single tumors doctors who have experimented with Keshe Technology
can tell you that you can remove this cell in a specific way by producing
certain systems where the energy transfer between the systems allows the
depletion of the energy of the material and once the mother seed of the pearl
has disappeared, the cancer has no strength. What we see is the tumor goes
black and then when it goes black it is a matter of time that the immune
system of the body of the man will more or less deplete and eat up
everything. You will see one of these in a few minutes.

25:55 K:
It was shown in the Rome conference by Dr. Rodrigo and for the first time
we will show it in the public. It is unimaginable what you will see; those
who have seen it because it has been on the internet sometimes. It is the
major achievement with the new technology. It is plasma and understanding
the change of not only the environment of the man but changing the emotion
of the man and then allowing the depletion of the cancer to a normal entity
that itself disappears our and is absorbed by the body of the man. In that
process sometimes we see the rejection of the pearl of the cancer, the
center of the pearl.

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26:44 K:
We have other cancers which are created by accident, and sometimes the
same process of the emotion comes by hitting where something hits your
body. We see this quite a lot especially recently in what is known as car
accidents. Heavy car accidents can create the same kind of center which
then starts the center and it goes through. There is another cancer that is not
a cancer but has been part of the mans progress in the evolution of his life.
We evolve and in that evolvement of life to fit in the new environment, our
body cannot operate or does not see how to handle the new changes. What
we see now in many cases part of the evolution of the cancer comes with
women. Up to 100 years ago menopause in women was 25 to 35 years.
now in more nations where we see more national security we see more
sharing of the burden of the growing of the children by the society and this
figure of menopause for women is getting pushed to the 50s, 60s and 70s.
This in some women cannot go through because of the emotion that comes
with the change, we can see some evolutionary cancers that are very hard to
handle and extremely difficult to process and these count for 1 to 5% of the
cancers today.

K:
The accidental cancer is random and there is no date for it. But with more
and the more high speed accidents that we see, 5, 10 to 15 years later we will
see the beginning of cancer and when you go back to the patient and ask
them they say that they had an accident in such a place. We are seeing this as
part of the cancer system.

29:02 K:

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What is important for us today is that we touch on the emotional ways the
cancer has been handled. You will see DrR show the process of cancer
reversal in a way that can be distributed on the internet today. This is one of
the impossibilities in the world of science. Even 5 months ago the doctors
would have been going crazy telling you this was impossible, but in the
hands of highly competent and knowledgeable Dr. Rodrigo, you see the
change. This is because he understood the totality and he was not just
handling the tumor. He helped change the environment, creating a condition
of breathing, creating a condition of elevation of the soul which through the
elevation of the soul. This was done in a way that changed the expectation of
the emotion by raising the strength of the filter strength of the emotion. That
filter does not exist anymore. Now there is no reason to keep the
communication between the brain of the man and the tumor. In that process
where the brain has no more contact in the physicality of the confirmation of
the existence of the tumor, the tumor becomes redundant because it has lost
the reason for which it was created. Now if the strength was a 2 with the
elevation of the emotion at 3, there is no room for 2. You change the
environment of the emotion and what we call the filter strength and then you
see the change in the position. Now once you elevate the soul, it is a matter
for the physicality of the body of the man to lose something that suddenly
appeared here. Through the immune system and the reduction of cells, the
creation of new cells and then you will see the changes.

31:09 K:
What we would like to do is go to Dr. Rodrigo because they said the proof of
science is in the black box theory which means we keep a black box of the
body of the woman. Dr. Rodrigo will take it and if any doctor in the world
can tell us how such a thing is possible then we have a new magician and
our magic is the world of plasma. We show this first and then go to the
next step. We have a number of people want to show or explain how they
have overcome cancer and how we know in one case that the wish of the
person is so overwhelming that he does not want to be able to carry on
because there is something in the background which is only to her or him
only that wishes the termination the way he or she likes. We cannot override
the wish of the man and it does not matter what we use. Thy shall not steal.
A physician cannot override but can elevate the soul of the patient so that the
patient sees a new life. And if that new life does not satisfy the condition he
or she can take a new course. I would like to ask Dr. Rodrigo in the
background to join us.

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32.34: K:
Dr.R is one of the heads of the earth council for South America. I will go
silent and I will take over when you finish.
33:41 Dr. Rodrigo (DrR):
I work with a group of doctors that work together to change the process. I
will show the video. This is a case of breast cancer treated by plasma
technology presented on
0339-2017 Keshe Foundation Spaceship Institute Universal Science
Presentations Medical, Rome, Italy. Recording can be found at:
https://archive.org/details/201703290000KFSSIUniversalSciencePresentatio
nsMedical
Dr.Rodrigo Vildosola: Breast Cancer Treatment with Plasma Technology

DrR:
Now I am going to present a case with breast cancer treatment by Plasma
Technology. But before that I am going to talk a little bit about my
background.
Completed Medical School in Mexicali, Mexico
Specialty in General Surgery and Plastic/Reconstructive Surgery in
Mexico City, Mexico
Fellowship in Plastic/Reconstructive Surgery in Madrid, Spain
Fellowship in Plastic/Reconstructive Surgery in Luca, Italy
Private Practice in Plastic/Reconstructive surgery for thirty years. I
have quite a bit of experience in this area.

DrR:
The Breast Cancer Patient was a 36 year old female. It was the left breast,
lower-inner quadrant. The core biopsy results were invasive ductal
carcinoma, nuclear grade 3. She chose not to follow traditional
chemotherapy and came to me 6 months after she was diagnosed. This is a
very aggressive cancer. We are going to see some photos that I will warn
you are very graphic. This is a case that was sent to me. When she came,
this patient with breast cancer already had a biopsy. One week after the
biopsy the breast started growing enormously. The patient was put on
antibiotics for three weeks. She refused to do surgery and chemotherapy and
chose alternative methods of treatment.

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When she came to me she had no energy, high fever, pain in her left breast
that resulted in sleepless nights. When she came to me she asked if I could
help her and I said that we would try to do the plasma energy therapy. I had
seen beautiful results and she was welcome to try it. I invited her to stay
inside a machine you will see later on. I asked her to see what the end result
would be. She stayed for an hour and then went home. The next day she
said the previous night was the first time in several months that she was able
to sleep without any pain. She was willing to start the plasma energy
treatments.

The only blood test that she had showed Leukocytosis (due to the infectious
process); this meant the white cells were increasing. She also had anemia
that continued to require blood transfusions. Before I address this patient and

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the cancer I would like to explain how we as doctors in plasma technology
are addressing the health issues. We divide them into 4 steps:
Physicality, Energy, Emotions and Soul

The physicality is which all doctors see medicine as the physical and treat
only in that area. As doctors we work on the physicality all the time. We
remove tumors, we give treatments of pills, tablets, etc. and that is the only
area that we as doctors work at.

When I ask the doctors about energy they always refer that energy comes
from the brain. I say to them that the brain is electrical impulses and is part
of the physicality and the Energy, Emotions and Soul are different. I would
explain every single one. Most of the doctors dont address the Emotions.
Most doctors see emotions as relating to religion and they dont address the
emotions. Now the way we address any disease is the elements of the body.

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 The physicality that we see is medical plasma and the doctors are seeing the
elements of the body. Every element of the body has its own gravitational
magnetic field so we can work on area. 96% of the body is made of 4
elements: Nitrogen, Hydrogen, Carbon and Oxygen. We have to understand
that 96% of plants and animals are also made of the elements. The other 4%
are the other 27 elements so we need to balance the body with the 96% made
up of CONH (carbon, oxygen, nitrogen and hydrogen). We dont need
millions of medications if we understand the plasma technology. We need
to know the kinds of metals are in the body and we can change the disease
process. We have to understand how the life is made in this world and the
elements of the body and where those elements come from.

In order to understand the body we have to understand the macro universe.

Everyone knows the sun has a magnetic and gravitational field and the earth
has magnetic and gravitational fields. These fields create life. The beautiful
light we see during the day that we call the sun actually is not the sun. It is
the light that happens between the interactions of the magnetic and
gravitational fields of the sun and the magnetic gravitational fields of the
earth. We see this light here. That interaction brings the elements to earth
which are carbon, oxygen, hydrogen and nitrogen. We are made of these
elements. This plasma technology duplicates this effect and we can bring
these elements into the environment. That is what we do.

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 If it were a sun then why is it completely dark when we go to space? If the
sun is so big why doesnt it light up the whole universe and space which is
completely dark? Not only that when we go out (to space) and you see those
videos or astronauts working outside of the satellites, you see no light, no
stars. So that light is inside of the interaction of the stratosphere of the earth
and the sun which creates the light. The importance of that friction that
brings elements in all the universe is all the elements we see on the periodic
table. What happened in this particular place between the sun and the earth
there are certain elements which include carbon, oxygen, hydrogen and
nitrogen. That means the earth and all living things on it are made of these
elements.

96% of our bodies are made of these elements. 96% of the structure of the
bodies of the plants is made of these elements. 96% of the bodies of the
animals are made of these elements. The rest of the elements are part of the

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earth. So that is important to understand why this technology is capable of
imitating and replicating the effects of these fields and bringing and creating
this energy. So we can add those elements and more of other elements to
create an environment so that people are able to be in the environment to be
able to change ourselves, to be able to regenerate and correct our cells. We
live in a world with so much pollution and imbalance of the elements that
they create diseases. So this environment that is created in the body gives it
those elements that will be able to change and reconstruct and build it.

The body is made of up 96% (CONH) carbon, oxygen, nitrogen and

hydrogen. The body is made up of 75% H2O. Once we understand the
interaction of the amino acids, and the body being made of 75% H2O this
releases the energy of the body which is Hydrogen. Let me give you an
example. When we are thirsty and we have been working a lot we need a
little water because we have been sweating a lot and we feel weak. And the
solution is to drink several sips of water. Normally the water has to go
through the mouth and the stomach and so forth and the body takes the water
throughout the body to the cells. But actually what the body needed was
energy so when we took in the water and the water is changed into plasma; it
releases the energy out of it to every part of the body.

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The way we see energy in the body is so different. There are a lot of devices
that can prove that we have energy around the body and there are people
who can see the energy. We have a doctor in the medical group who can
see the energy, Klaus D. the way to understand this is when we are thirsty
and need water every cell of the body needs the water so we drink the water
and wait from minutes to hours to get this to every single cell. But as soon as
we have a sip of the water we feel the effect because the hydrogen in that
environment touches every single cell in the body. This is the plasma state.
We have proven that the body is a plasma organ and not just physicality as
we have though of it. Once we understand how the body works and how the
body is the ways of treatment are going to change dramatically. So we have
energy in the body that connects every cell in the body. I will give you
another example. If you stop breathing for 20 seconds or a minute,
Every single cell needs oxygen and is crying for oxygen. Just hold your
breath for 20 seconds, less than a minute, and every single cell of the body is
crying for that little amount of oxygen. As soon as you breathe in the body
responds to the oxygen. Even when you breathe in the oxygen hasnt
reached the lungs and alveoli and it has effects instantly in the all the cells.
So we have the feel throughout the body. That is the way the body works.
While we understand that the body has so many connections; we can
connect and make so many changes. We have to carry the oxygen through
the red cells of the body and it takes a lot of time. But we have the field of
energy around the body and when the air passes over the top of the tongue it
changes to the plasma. It leaves the oxygen and goes to every single cell in
the body. We have this energy field around us.

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45:03 DrR:
Another way of thinking is that with the emotions we have also said in
medicine that 98% of diseases are psychosomatic. What does
psychosomatic mean? In the medical field they say that psychosomatic
means stress. Stress is a bad word and means nothing.

Stress means there is some type of hyperactivity of the brain or the body that
will have to shut it down. We have given pills to shut down the brain
instead of addressing the emotions. We say there are stress and some kind
of hyperactivity and we give pills to shut down the brain, to calm down the
body and to relax and that will fix or change the environment of the body.
We dont see that; I would say that stress is a very bad word and I would say
that 100% of diseases involve the emotions. Let me give an example about
the emotions. Look at Alzheimers. Mr. Keshe has given us so many
examples about this. What has happened with Alzheimers? According to
medicine the brain is dying. Why is it dying? They take an MRI and see a
black spot on the brain and say it is dying. People with Alzheimers dont
like the present that they are living. People that normally move from one
country to another and dont like that new country live in the past, from
one house to another house or move in with different family members. They
have changed the environment and the reality they lived in. That is why
they remember and live in the past. They dont live in the present but inside
the past in their brain. Inside the brain in the subconscious is says the
present doesnt matter and it starts to shut down the brain, the body. Then
the brain is not connected to the present because they live in the past. That
why people start exhibiting depression, because they live in the past. We
have to address the emotional issues in order to bring them back to normal.
This is not part of this presentation but it is part of the emotional connection
to a disorder. When you change the environment people come back to their

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reality. I didnt have time to present people with Alzheimers who were in
bed, not moving, not blinking, being fed with feeding tubes through their
noses. When we treat them with these ganses people come back to reality. It
is incredible what we have seen. So the emotions affect the whole body.

48:40 DrR:

In the 4th level we see the process of any disease is the connection to the
soul. As I said many people think that this only another part of religion. We
are not the body; we are souls living in this environment in this life. When
we are able to connect to the souls it means that no emotion is involved in
this and nothing bothers us. Nothing bothers the body, so the body heals. It
is incredible and that is the beauty of helping us get rid of the emotions and
touch the souls of ourselves and be able to change everything. So how do
apply this technology? We have a protocol that we have created with the
medical team. We do this for every patient.

19
It doesnt matter if they have cancer, diabetes, hypertension, Parkinsons or
whatever disease the body has. For every person we address the disease this
way. This is the protocol we follow for any patient that includes using the
breathing device for every single person we treat. 95 to 98% of the diseases
involve emotion so we give these devices to every patient in treating the
disease. Drinking water Gans brings balance to the body. We use the
Health Plasma Units to target the organ(s). That means that once you are
inside this health unit it will heal you. It is going to start some changes
inside the body. We have to target the body and understand what part of the
body has a problem. In a cancer the body may have more of an element that
may need to be removed (such as calcium). Mr. Keshe has explained that
the seed of the cancer has a greater amount of some kind metal and we can
change that. We can construct something in the body if there is a lack of an
element that keeps the body from being in balance and bringing about
changes. We give the body what it needs to repair any part of the body, any
organ in the body.

We use the breathing device to target emotions. We use the devices that use
the water ganses: ZnO (zinc) water gans50% and CO2 water gans50%.
These are mixed and we target the emotions. If we put a person inside a
health unit without treating the emotions it is hard to bring balance to their
body and their body will not be able to reconstruct itself and change the
problem or the disease. I would say the 100% of the people that we treat, we
have to address the emotionsall of them.

20
52:22 DrR:
People all over the world have created devices in order to get this
environment of ZnO and CO2. I use this tube myself. I have a 5/8ths tube
and a 11/4 tube. The bigger tube wraps the smaller tube that is filled with
the liquid ganses of CO2 and ZnO and people breathe the air that surrounds
the inner tube (not in the tube). When people come to be they ask how I
know there is energy inside. I have two plastic balls that have the liquid of
CO2 gans inside. I tell them to put the balls closer to each other and they
feel the energy like magnets. It is energy interacting between the ganses so
every person I treat I have them use a breathing device. As soon as they
start breathing a few days later they are starting to feel a lot better. They
know they have emotions and those emotions dont affect them any more
and they feel more relaxed, able to sleep and think better. We have to
understand that we create our own reality. If we have access to the mid-
brain we have the control of the emotions. Let me put it this way: when you
have access to the mid-brain you can access everything and you can create
the reality you want. If we have problems and drama in our lives, we
created this drama in our lives and emotional problem we created this and
change the body according to the emotions and reality we wanted to create.
What we have in the mid-brain we create a reality.

54:13 DrR:
How many master teachers do we have right now to teach us to create a new
reality that has us focus on something loving and beautiful and a different
environment? If we have so much drama we created it and we cannot create
a different reality. In order to get to the mid it is like we are having a funnel
or water with a bottle neck. There is a small window of access to the mid

21
brain. Like I said it is like a funnel. We have so many emotions that cover
that window. So you have to get through those emotions that create that
reality. So the technology of using the gans waters of ZnO and CO2 should
remove and clean that path so we have clean, open access to the mid-brain
so that we can create a different reality and we stop thinking about the drama
that created the disease. It just disappears. We have so many doctors in the
world that treat the emotions and we see results even in traditional medicine.
So this works; we created the diseases and not just cancer, but any disease.
We have access to the mid-brain, the root of those dramas and we can create
anything. That helps a lot.

The other step is drinking the water. The CO2 is to target the cell
connection, neuro system and emotion. The ZnO targets the Emotion. We
use the CuO (copper oxide) for the muscles, ligaments, and as a disinfectant.
We can use every single element and we can create any elements that we
need in order to bring balance to the body. We can bring change and have
the body regenerate. Also we use CH3 for energy and the way it works is
that we have the 75% of the body as water (H2O). There are 2 molecules of
hydrogen in the H2O and when we get the CH3 it has interacted with the
water of the body and hydrogen is released as the energy. That is how we
get energy. We have to understand a little chemistry of how the body works.
The CH3 is used for energy but in particular is not given to cancer patients.
We never use CH3 on cancer patients because CH3 gives energy by
releasing hydrogen to every cell of the body including the tumor cells. Even
though the cancer patients have no energy and are weak we have to be
careful not to give them the CH3 as we dont want to energize the cancer

22
cells. Even though people are weak we dont want to give the CH3 to give
extra energy to the tumor cells and they will grow as well.

Also, people with different diseases like cancer; we can give energized
plasma food. We can use a device like this with the plasma food gans liquid
inside. We can use patches filled with the food liquid gans that we put on
their back and CO2 patch on the front of their stomachs. We have a
different twist on giving food to the body because the body works on a
plasma state. We dont to eat anything. The body, once we have eaten food
and it goes to the stomach, the stomach turns every element that we eat to
plasma. We can give another lecture on this and its a beautiful way to
understand how the body works. When I give lectures I explain to people
how the nano technology is made and how we create energy. When we nano
coat the layers on the copper plates, we see that nano coating the layers is
similar to the nano coating the body does as layers of nano coating on every
organ. We work with plasma and if you give the body the plasma it needs, it
will gather through the skin. This is another way to understand.

23
If you want to know more about how to use the plasma this Plasmatic First
Aid chart is a way of understanding how to use the plasma energy. You can
go to www.keshefoundation.org or Keshe Foundation on facebook. Every
member that joins the KF can find the plasmatic first aid charts that explain
how to use the plasma. Everyone could have this in their homes as a
different way to have plasmatic first aid.

1:00:35 DrR:
I created these plasma health units from blueprints that Mr. Keshe gave us.
A lot of people around the world are making these kinds of devices and
anyone can use whatever they want as the structure. The main thing is the
coils inside that Mr. Keshe taught us to make. They create an environment
when you are inside the unit that you feel the energy. When I give lectures
people say to them energy is peace and love. When we talk about energy

24
with the health plasma unit once you are in the environment of the unit you
feel the tingling and the heat of the energy going through the body. Once
people go inside it feels good and it will help you to have the elements you
need. On the bottom the unit has coils mixed with CuO (copper oxide) and
CO2. In the middle that covers the whole body is the gans of CO2 and at the
top is ZnO. The wires, the plasma batteries are made of ZnO and the gans
used have ZnO; this controls the emotions.

01:02:23 DrR:

To understand the effect of this technology we have to understand that in

order for us to survive 80% of the energy comes through the skin or through
breathing. 20% of the energy we need to survive comes through the food
that we eat. That 20% of food also reaches us as plasma energy. So once
we understand this technology it is a different way to treat the patient and
they can receive energy through the skin or through breathing. So if 80% of
the energy comes through the skin if we put the elements in the environment
that we need our bodies will take them. This technology replicates the
effects of being under the sun and receiving all the elements of nitrogen,
carbon, oxygen and hydrogen from the environment and feeling great. We
need the sun in order to survive. We are given nonsense that the sun only
helps to synthesize Vitamin D. But it elements the body need in the form of
the amino acid proteins (CONH-carbon, oxygen, nitrogen and hydrogen) the
body needs. This is what we need from the sun and we are creating
environments that we can get the elements the body needs. We can create
any other elements since the body is made of 27 elements. If the body needs
some of those elements we can create it as a plasma and give it to the body.

25
I created a different health unit thanks to Mr. Keshes teaching. We created
this unit using plasma inside a tube that is inside another tube. The inner
tube has different liquid gans that the outer ring. Normally it has a mixture
of ZnO and CO2. Just this liquid can change the body and give the body the
elements it needs to start repairing and changing itself. I would say this
brings miracles. This is a beautiful unit and people can sit inside for minutes
or an hour. When they do this one or two times a day it is sufficient.
Staying all day in the environment will not repair everything. Using this has
to be done with gaps between the use. What we are doing is retraining the
environment. We have so much pollution in our environments that we
create imbalance in the body that start making diseases. We have so many
poisons on the food that we eat and chemicals and pesticides everywhere.
These chemicals in our bodies start creating diseases. So this environment
inside has created a beautiful environment and the body has to remember
how to work and function normally. So the same they body creates diseases
is the same way we have to retrain the body. We train the brain to do the
opposite of the condition that needs to be change. The body has the ability
to repair itself the same way it does if we cut ourselves. If have a small skin
cut, the body can repair it. The body can repair every part of the body even
the brain tissue. Doctors say that brain tissues cannot be repaired and we
have proven many times that the brain tissue can re-grow. We can re-grow
any part of the brain and nervous system.

1:06:46 DrR:
We have proven this and I invite people to be involved with this technology
and attend the meetings. There are a lot of students all over the world giving
lectures. We can find in many countries and many languages the

26
technology. We have no barriers or limitations for understanding. There are
a lot of people all over the world teaching this technology in every single
language. We want to bring different environments to the body.

We have the privilege to have an incredible person named Klaus D who can
see the energy from any devices. He asked me to show him these devices
and he saw the energy around the devices. He said there was toroid field of
energy from the unit on the left and it goes back and forth across your body.
This unit on the right creates a vortex. In the unit on the left has a see-saw
effect and pulls the energy they need to release. The unit on the right creates
vortexes connected to earth so whatever the body has to get rid of goes to the
earth. These are 2 different approaches. A lot of people around the world
are making the devices in order to bring balance to people. All this
technology belongs to you and the world as Mr. Keshe has said. The way
we used to see invention of devices is that people who created the devices
created patents and kept things to themselves to make money.
The beautiful heart of Mr. Keshe is that he has created all this technology,
patented it, and whoever wants to do something with the plasma energy, he
has given this to humanity. Whoever builds something related to plasma
does it for humanity. There is no more mine, I created it and Im going to
make money off it. all this technology belongs to humanity and when we
create something it is posted on Facebook, and different websites to give
people access to it. They can start replicating it and changing it. This
technology is for everybody and nobody owns this technology. Humanity
owns this technology as a gift from Mr. Keshe. We have to take advantage
of this technology to change the world.

27
1:10:06 DrR:
The plasma energy brings fields that balance the body. Plasma always tries
to bring balance to the body, the universe, the whole galaxy. So whatever
happens in the body, the body is trying to bring balance and change the
condition of disease in the body. We create a different environment using
the different liquid gans to change the body by adding something the body
needs or by removing something from the body to create the balance. If you
have a knee problem with the cartilage and are waiting for a knee
replacement, if we have a piece of that cartilage, once we bring that
environment around the knee, the knee can repair itself and we dont need
the surgery. In the future we wont need any surgery. With this technology
we can remove anything or we can repair anything. We dont pills,
injections and surgery. It will all be gone. We are working together to bring
this technology to people. We are testing it. Humanity, often when
presented with a new technology, wants results right away. We are learning
and we have a group of doctors that are learning how to use the technology.
We are seeing results and as soon as people have results there is a website
where people can post them. We invite you to use the technology and share
whatever you change. Any changes or experiences in your body we ask you
to share with us. We want everyone to share any experience they have with
this technology. Bring something to humanity.

01:12:47 DrR:
The last protocol we use on patients are the CO2 GANS Ampoules.

28
We have trials going on that are using CO2 Gans Ampoules for cancer
patients who cannot stand in the health units or come to use any of the
devices. We have this new way of treating these patients and are having
beautiful results with the use of the gans water even with severe conditions
of HIV patients, Malaria, Ebola and conditions that we thought there was no
cure for. Now we can bring balance to the body so that the body can change
and repair. It can reconstruct itself and we are bringing balance to the
balance. The technology gives the body the elements it needs to repair itself.
That is what we do. 96% of the body is made of CONH (carbon, oxygen,
nitrogen and hydrogen.) When we give the body those elements in a plasma
form the body can start changing its environment.

01:14:03 DrR:

Now we go back to the patient with the breast cancer. I like to explain to
people how this technology works on the body so they can understand how

29
we can have these results. This is the patient with the big huge tumor. First
we had to analyze the emotions.

The left breast is between the mother and children. This is the breast most
women feed first for the baby. We are connected to the mother through the
left breast. Women breast feed from both, but most of the time they start the
feeding with the left breast and this is the connection of the mother and the
child. When you have issues with your mother or child you have the
connection with the breast that is connected to the love emotion of that
person. When you have issues sometimes with them you create something
in your brain that you want to cut or get rid of that connection. It might be a
bad connection with your mother or your child. What is that connection?
Your breast is. The brain says that the mother is connected to the child and
it will get rid of the connection through cancer. If the brain creates the
disease, we can do the opposite. When we treat the emotions we do that the
same we reconstruct the breast. The right side is connected to the father. I
want to take advantage to explain how important the breast is. We know
that we have 5 organ senses. We use the eyes for sight; the ears for hearing.
The mouth is for tasting and the nose for smelling. We have the skin for
touch. But we have another organ sense and it is not just only for women. It
is for everyone. The organ that controls the emotions is the breast which is
connected to emotions even for men. It has a big antenna. And we control
the emotion. Here is another example of this: the breast is a big antenna that
picks up all the emotions. If you watch a soap opera or any movie and you
watch that facing the TV, all emotions come to the breast and you feel that
energy. I invite you to watch that movie or soap opera on the side, not
facing the TV. You see the effect is totally different and you are not
receiving that energy straight to the body. So it is as though you are covered

30
with protective metal and you dont feel the same way. The emotions come
through the breast. The whole body works so differently.

01:18:27 DrR:
Back to this patient now; I get excited everytime I explain this to people
because it is so beautiful. As I said to all patients with cancer, we do a blood
test to determine which metals are high in the blood. The one we find higher
is the one that is involved in the cancer and that will be the seed of the
cancer. Once we understand the magnetic gravitational energy, how we can
explain that is that something is pulling and creating the cells and using the
energy of the body people who have cancer dont die of cancer; they die
from the lack of energy and they dont have energy. The tumor pulls all the
energy and people die from the lack of energy. Something inside the tumor
or the cancer pulls all the energy. With this plasma technology we name that
point as the gravitational and the stronger gravitational field that pulls the
energy. We have to create a different environment outside of the body in
order to change that strong field of energy inside the body. Once we
understand and know the metal energy that is pulling the energy, we make
gans of that metal, whatever it is. In this case the calcium was high but I
have seen breast cancer with arsenic involved in the tumor. Some other
people had lead or mercury. Whatever metal we find in this tumor we have
to make the gans of that metal in order to create the different environment.

01:20:34 DrR:

This is the sample of the metal that we had to find that was the seed of the
cancer and in this case it was calcium. The way we make calcium is easy.

31
We have chicken bones from chicken you have cooked for dinner. Cut the
bones in small pieces and boil them in vinegar 5 times until they become
like jelly. Once they are like this, get rid of the vinegar. Then put them in
caustic and add boiling water. That starts to create the nano coating of the
calcium and energize the molecules of the bones. There is a lot of teaching
on making gans of food or elements and you will find them on you tube and
knowledge seekers workshops. There are instructions for making any kind
of gans. This was with the bones and left for 6 days in the caustic. After 6
days it is rinsed with distilled water and you clean out the caustic that is
salty, an alkaline solution. When we get rid of that we add CO2 gans water
and after 24 hours we have the gans of calcium. This is the way to do it and
its the same way you do the gans of food. This is the process for doing it.

When you make the patches you can use any element, any plasma inside of
that and create the element.

32
Once you have the patches of calcium we create different fields with 2
patches and we put them on the sides of the breast. In this case with a huge
cancer we put one patch on the side of the tumor on the left breast on the
right side. We put the stronger patches on right side and the weaker on the
left. What does this mean, the stronger and the weaker? The stronger has 3
times. Once we create the plasma and put them on patches, there will be 3
mm of patches on the right side and 1 mm of patches on the left side. The
ratio is 3 to 1. That environment creates an environment of the interaction of
the fields and we have calcium inside. We have different strengths of
calcium on the outside of the breast with stronger on the right side and
weaker on the left side. So it creates a magnetic gravitational field in
between that brings the balance and changes the environment. Little by little
that seed spot starts disappearing or becomes part of the body. Remember
the body has calcium but in normal concentration.

01:24:28 DrR:

33
If this is a small breast with a small tumor the higher concentration goes on
the back at the breast level and the smaller concentration goes on the front.
We create an environment with this energy that goes in between.

Whatever is inside blends to the energy fields or elements and changes the
environment. This is the same way if we want to repair or add something
we can do it the same way with the patches and bring the elements inside the
body in order to bring the change.

As the breast started opening as you see in the photos and Im sorry to
show these graphic photos but it is the only way to show thisthe cancer
was very aggressive and there was a lot of infection as the cancer was
destroying the inside. The cancer stopped growing and all the tissue started
being rejected.

34
01:25:43 DrR:
This is the see that crested; it looked terrible and stopped growing. When
this patient saw the doctor no one wanted to touch it. She was taken to the
hospital because the doctors were afraid of this. No one wanted to touch it
and no had any experience with this. Thank God nobody wanted to touch it.
We kept putting this patient inside of this environment. The body grew so
big and then pieces of the tissues started coming off the body. When she
started to reject pieces the calcium inside was very high. There was
bleeding and she had to have blood transfusions. They didnt want to do
anything on her. I asked them to do a biopsy and no one wanted to do it.
The tissue that grew on the left side had the seed dying. The body was
rejecting the tissue and to start to shrink because a lot of the breast tissue
was destroyed inside.

I asked the doctors and we had to go to 5 different doctors to find someone

to do the biopsy. They said it was cancer and they didnt need to take the

35
time to do the biopsy. We insisted and we finally found a doctor who would
do the biopsy because he wanted to prove that the cancer was still there.

01:28:12 DrR:
This was the CT Scan showing the reduction of the tissue and the lymph
nodes. At the beginning the lymph nodes were very big before she went
through this process with the plasma technology. Every part of the body
will start changing. We were finally able to get a biopsy of this:

This report said there was fibro connective tissue with extensive coagulative
necrosis. There was granulation (scarring), coagulative and calcification
indicating tumor necrosis.no evidence of viable tumor seen in current
biopsy. There was no tumor any more, just the destruction with the dead
tissue. The cancer was gone. We work on this patient to keep this

36
environment. The body is still changing and we are still using the
technology to change the environment for this patient. If we need surgery
(reconstructive) we have to wait at least 6 months to get all the tissue
softened and then we can start the changes for reconstruction but still using
this technology.

01:30:06 DrR:
Thank you; I will take Questions if there are any. I will stop sharing and
open to all of you.

01:30:30 Rick:
Let me remind the viewers if they have a question they can put their hand up
and I will promote them to panelist.

01:31:04 K:
Thank you very much Dr. Rodrigo; this was an impressive presentation and
this actually shows what the technology is about. We have to understand
that this is not the only way that breast cancer shows itself. We have some
breast cancers that are internal and are closed and somehow created
internally. We dont see the tumor without the X-rays. And these cause
what has been said the end of life, the termination of the physicality. There
are a number of things that have been raised here and this process took 60 to
90 days from the start to the end. We do not see any secondary cancer in the
body at this moment and it shows there is no need for the operation and once
you elevate the emotion of the man in respect to his soul, the body will take
its position. Our features are decided by our emotion in respect to the
energy of the soul of the man.

01:32:33 K:
There is something that I keep repeating and it has been repeated by Dr.
Rodrigo. That is that there is a massive misunderstanding about the position
of the soul of the man and this misunderstanding has led to a lot of
problems. In the present time we imagine at this time the soul of the man is
somewhere above the head on the body of the man.

37
We have thought that this was the position of our soul (above the head). So
we have nothing to do with the soul; it is something (we think) that is
outside of us. But with the present knowledge that we have gained we now
understand the soul of the man is within the center of the brain. That is why
your soul as a source of the center of the energy acts as the sun of the life
in the body. It takes rays inside the body and as you create different filters
around it, you dictate in reality different physicalities.

This is not fully understood the soul is not outside the body. If you can look
at MRIs you get nowadays. And if you look closely you will find the soul of
the man in the brain of the man in the bottom part of the brain.

38
01:34:17 K:
We will explain this very soon how the brain of the man is created. As we
go into more depth of the knowledge we open more pieces of knowledge
that has been hidden to the man. This will change a lot. So what happens is
that this the position of the soul and your emotion goes around the soul of
the man and in that position your emotion in its time and interaction leads to
the physical manifestation of the physicality of the man in his emotional part
and in respect to the physicality in the replication of the body of the man.

01:35:11 K:
We see the hands and the fingers on the side of the ears, we see the upper
arms on top of the brain and we see everything to do with the shoulder and
everything else which grows inside.

39
This has been one of the mysteries of the creation where man thought his
soul was outside his body. But in fact
The soul of the man in operation is the essence of the creation of the man is
in the center of the brain of the man. That position allows the fields to be
affected by the emotion and that emotion reflects in the physicality of the
man. And now we understand how we lead ourselves into cancer. Every
cell of the body of the man carries the emotional part as much as it does the
physical part. So this has been part of what we see and how we change the
condition because all we do as present people is to change the filtering
thickness.

If you change the strength of the filter and it increases in strength at the
lower strength there is no cancer to be created and that is how you disarm
the body from its own tools of destruction of itself. In so many ways and
places once man understands this a lot of things come to order. In the
present understanding you call energy points the different chakras. What
you call the energy points are controlled by the body of the man itself.

40
01:37:07 K:
Then you understand that what you thought to be a chakra above your head,
an energy point that you called the position of the soul, is within the center
of the brain of the body of the man. This is what is important to all of us.
For the first time we can position our soul. If you translate or re-define the
soul as the center of the energy of the creation of the entity of the physicality
of the man then it is easier to define and interact with creation. It is not a
mystery that there is something that leads to our creation. The sun is in the
center of the solar system; we dont see the sun outside and that it creates the
earth and the other planets. How can it be any different in the body of the
man? The soul of the man sits within the structure of his own sun. if you
look at the whole structure of the brain of the man or any animal, we see it.
We want it to be mysterious but in fact the essence of this is that as this sun
soul radiates out it leads to our creation. If you put it together in a different
way there is no difference between the sun and the body of the
Man.

.
The sun sits in the center and radiates out equally and so does the soul of the
man. Due to massive amount of material that we fit around it we have create
a faster reduction in the fields of this and this is what you have. In that rapid
reduction you lead to better, faster physicality. If you look at the sun as the
rays go out the higher and further and wherever it goes the plasma of the sun
leads to the creation of the physical parts such as the earth, Saturn, Venus
and in the energy transfer in the center with the shell of its fields, we create
what we call the solar system. So is the body of the man and the brain has
become the filter.

41
As the sun rays go out, the further the rays go this leads to the physical part
of the earth, Saturn, Venus and the rest of the solar system. The brain is the
filter in the body of the man. Here (the diagram showing the sun) the mass
of the filter is less so the slowing down of the fields is much slower and so is
the expansion of the size and the body of the physicality. In the brain of the
man the physicality is different where actually the filtering is much stronger
and in compacted fields so you see the physical structure. There is no
difference in the world of creation. This is what we can now interact and
now we feed the emotion and by feeding the emotion we change the filter
strength from sadness to joy. Now we understand that every emotion has
field strength of giving and taking. We can change it; what is pain to me is
not pain to somebody else. It could be joy. With this knowledge we can
decide to change. With that change because the strength changes the fields
in respect to what was createdthe disappearance of the cancer. All we do
is we continuously surround the body and enter the body with fields of
plasmatic condition that the body takes its position to the elevation of its
own magnetic field of the emotion and change of the cancer. This can be
any disease.

42
If you understand this then you understand that in the coming time when
man travels in deep space the strength of fields that man creates around his
soul will dictate the shape of man in deep space. Then we become the
chameleons of space.

01:41:21 K:
In a way through the process of the health section we opened the door to the
reality of creation in the universe. These are at the moment are very much
what it is of the present limited understanding of the man in respect to his
own life. But what we have done we have used for thousands of years we
have used herbs and materials which could effect. In the recent past we
increased the knowledge into the hand of those who could compact it and we
have called them the pharmaceuticals and different names such as tablets,
injections and anything else we like to only affect the physicality. We never
understood that the emotion of the man is connected to zinc in totality. Once
we understood this, it changed the course. Now we can change the strength
of the emotion in the physicality according to what we put in. On Thursday
I will explain this more in the public teaching and then we will understand
more how some of us are vegetarians and some are meat eaters and how our
lives change according to the amount of energy we absorb.

01:42:47 K:
It will be very interesting; we open a new dimension in teaching on
Thursday and you will understand. What has happened to us in the past few
decades is that we have given our trust of our world of health into the hand
of what we call the man of science and the man of science according to what
their financial backers have said have cheated and depleted the life of the
man. Now in past decades we have given our trust in the hands of people

43
who have managed to control legislation and push anything they like to
affect our physicalities and we call them pharmaceuticals. In fact they have
been helpful but in so many ways all the medicine we have is one way.
Medicine treats the physicality without understanding the emotion which has
come into play.

01:44:07 K:
One of the emotions that resulted in the abuse of medication is what we call
the beautiful people or what you call schizophrenics. The world of medicine
has never understood that the world of the schizophrenic is a world of two
entities within the body of one man. We always called them the twins
because we could see they had two physicalities and we call them the
Siamese twins that share part of the physicality. But because of our own
lack of understanding we never understand that two souls can live within
one body that can share the body. In totality in the world of creation we call
them the twin stars. When you look at the twin stars we dont look at two
individual stars; we look at the collective effect of that entity in its
environment. So in so many ways if the world of medicine ever understood
this they would not have created medicine for the schizophrenic because
they know it does not work. They have understood nothing in the reality of
the world of creation that there are two souls within the structure of one
physical body. No medication can change this unless you bother one and
you elevate the strength in the emotion in one that affects the emotion of the
other. If the man of medicine could understand that there are two or three
entities in the body of the man you call a schizophrenic you will never give
him medicine. You will ask his name and what does he want to be known
as. How does he want to present himself? And you will find out that you
speak to different souls. They may have different language and they may
dress differently and they react differently. They show different emotions
within the physicality of the one who carries too many (souls). This is the
lack of understanding of the man in which we create medicines for the things
we dont understand and then because of our lack of understanding we
enforce it with castration and imprisonment and put these people in
institutions; we should be in there, not them because in reality we never
understood the totality of the creation. We are too physical and we dont
understand. So maybe with these teachings as with cancer we have become
through our medicine the cancer of life of these people who are in entity the
twins and the triplets. We have to see it to believe it and speak to them the
language that they understand. You are speaking to 2 or 3 souls that are
confined within the same body. I have taught how this happens many times.

44
At the same time as the pharmaceuticals have created their own way of
control that nobody else can afford to do it and they have brought in the
clinical trials where we kill more to prove more of how ignorant of the
knowledge of creation that we are.

01:47:20 K:
At the present clinical trials when want to introduce something new create
different animals. You allow animals to give birth or to be created and born
and then you infect them with the diseases that are bothering you and you
are too chicken to do it yourself so you give it to the mouse and to the rats.
Then you will see what it does to them and then you say because 99% of the
body of whatever animal is close to the man so we can barely or maybe use
it for ourselves. But on the other hand the man never understood that the
creation of the amino acids from the atmospheric part of the body of the
planet has led to the creation of the man. That is why all the animals have so
much closeness to the man. It is because man up to now never understood
that he is made out of 3 parts of this beautiful planet that we call earth.

01:48:17 K:
Earth has the gaseous part, the liquid part and the solid part of the planet.
The amino acids of the body of the man come from the gaseous part. And
that is why most of the animals on this planet are so close to each other.
Science never understood that the totally of life on this planet depends on
this. Whatever is made is of the gaseous part which is the CONH (carbon,
oxygen, nitrogen and hydrogen), the common elements. They interact with
the metal part or the liquid part of the environment that we call the surface of
the planet and this leads us to different kinds of creation. On Thursday I will
explain this very clearly and how animals created under conditions of certain
strengths have the same features and why the man, the cat and the lion have
two sections of the brain and how he comes to have 2 legs, 2 arms and
everything else or they become the birds with the wings and the legs. For
the first time I will disclose this understanding so that the man will
understand more about himself and how he attains his physicality and he
understanding this how he will change physicality in different dimensions
when he enters the universal community.
******
Resume transcribing here.

01:49:49 K:

45
In this process of understanding the structure, the present pharmaceuticals
creates another headache and are pushing man to the verge of absolute
insanity. This insanity is why do we have to kill animals for us to be sure
when we use something we are too cowardly because it will damage us. I
said sometime ago if a condition of testing is good for us and that important
then every restaurant and carry-out should have the FDA certificate that the
food has been tested on the mice and has killed no mice. But we dont do
that. We decided that wherever there is a lot of money we attach to the
physicality the control. Nobody controlled my grand parents and great
grandparents for generations when they were the medicine men. Now it
makes a lot of sense to make a lot of money and we have the controls of the
pharmaceuticals and nowadays if you want to even eat a mint you have to
have the certificate from the shop that it is mint and what the FDA does with
it.

01:51:08 K:
For this reason to comply with the regulations that the material is safe and
stop criticism with KF, we collaborated with scientists in Tokyo. The
original testing was to show that these materials that we use that are copies
of the universe which we call gans that are packs of energy are non toxic and
dont harm us. Because there has been a lot of criticism that these things are
this and that, we went step by step, element by element, to find out which
ones have which effect. So we started with clinical step that we called
Phase One which is for toxicity and we will see this test done by the
scientist himself in Tokyo University and he will present the paper. this
paper is fundamental and will be the cornerstone of all the application of
what we call CO2 and ZnO. We need to do many of these toxicity studies
by the energy level transfer and not by killing animals. As I said before we
start this part we bless these animals through their souls the weakness and
cowardice of not testing this on ourselves. As I said before when we lose
those on the line that were to protect our lives, the military term is to stand
by the flag and stand beside us. We do the same for football players who
served us and gave us pleasure. Maybe it is time to stay silent for the souls
of the animals sacrificed to prove through these ridiculous conditions of
what we call medical controls. I ask you to stay silent for a minute and then
we come back and start the presentation by one of the most sincere scientists
I know. He is one of the most highly intelligent people I know and one of
the most honest men I have known on this planet. Please stay silent for one
minute. (a minute of silence).
01:54:43 K:

46
Thank you very much. If you were here with us in this room you heard
something strange; even the church bells started ringing. Very strange. The
Creator is with us. Let me introduce you to the scientist and many of you
know him and have met him and you have seen his presentations. He is one
of the leading scientists in Tokyo University. He is the man who took KF
into Tepco and he is the man who collectively worked with KF to eradicate
the conditions and the problem we saw with Tepco. All he got was to be
sacked from his job because he released the name of Tepco to KF. He is a
man of intelligence to understand why they were carrying on so many tests.
It was not for Mickey Mouse in Tokyo, but for Tepco because they had a
problem with the nuclear reactors (Fukushima). You have seen JK Japan
for collaboration he has done with Tokyo University as he was one of the
excellent senior students in the past. He did most of the examination and
most of the testing with the supervision of the scientists in Tokyo
University. We financed what was there from our side and this paper was
done by him and he delivered the beautiful papers which were read and
approved by the professors on Phase One and Phase Two. What we have
seen has been such rapid and perfect results we decided to publish the third
paper because what we saw as a result confirms the correctness of the
technology in eradicating cancer in one go. Usually we spend months to see
the results. With this technology and use of the gans materials in the data
which we present to you scientifically it shows that it does not need months
or uncertainty. The results indicate and show that in the case of intestine
cancer that applies to stomach and large intestine we have seen 100%
reduction in all cancers with the animals tested. 5 of the 10 animals were
sacrificed and the data showed no toxicity. I do not see any reason for the
other 5 to be sacrificed. This is enough. In that case and because of this
situation now in Tokyo University the final paper has been written done by
the scientist who has done it.

01:58:08 K:
I ask Mr. KF Japan to present every paper today step by step of Trial Phase
One Information delivery. Those of you from governments we respect you;
those from pharmaceuticals you will learn something new. Those third
world nations which cannot afford 150,000 to 200,000 for chemotherapy
(for each individual) your nation can achieve the results with less than one
dollar. But there is most probably a high guarantee that the cancer will not
come back. With this technology you sorted the root of it which is in the
emotion in most of the cases. I will go quiet and I invite our sincere partner
in development to take over. You all know him; he has given us some

47
lectures before and he will tell us step by step. I have asked him how he
produced the material so that you as governments and citizens can produce
this material yourselves. You have to understand that this is the disclaimer:
this is what we have seen and this is what is scientifically approved and has
been collected. I feel sorry for pharmaceuticals for all the chemotherapy
from today and I rejoice because I know that they did not work. They give
you a life sentence of 5 to 10 years, maybe a little less or a little more.

01:59:48 K:
This is our findings and this is what we see and it is the responsibility of
every individual to decide for themselves. We teach you how to make the
material because we are strong and we know this brings you benefit in
elevating the soul of humanity. In this process everything will be explained
in detail. We allow the governments, and we know they are sitting in the
background from different nations, and scientific organizations to ask and
put questions directly to us. This is your right. We dont allow you to
foreclose on this technology because the technology belongs to humanity
and is a gift from KF to the world. This time we dont make the mistakes of
the past. We share the knowledge through the hand of the scientists. We
will carry on with trials that you and the pharmaceuticals want to do and our
scientists at KF will deliver this directly to all of you. this means that if you
are a member of the pharmaceuticals and you want to be part of the work it
is your job to join us on the KF website www.cancerprocessing.org that we
have developed. You can there and go to the bottom of the page and you
will see that there are 2 links. One link is connected to those individuals who
want to carry on with the cancer process. The other one is for
pharmaceuticals and governments. We release the knowledge fully and
there is some we cannot disclose here as we did before so you can rapidly
develop these things in the background. We know government officials
from a number of African nations are in the background. We respect you
and this is a gift to Africa. This is for all of you and this means if you are a
member of the pharmaceuticals we will deliver these products across Ghana
and territory in the following weeks at the disposal of the nation. The
government will tell us how they want to handle it. There should be no
cancer in Ghana in the next 12 to 18 months for those who are connected to
the emotional part of the body of the man. We release these technologies
because Ii is the right of man to be free from the shackles of the control.

02:03:09 K:

48
I said to our reporters very recently: in these pages we see the cancer
touching the physicality of the man and we are giving the knowledge freely.
In the present environment what we have discovered and what we are
sharing is worth trillions. With this opening we hope the cancer sitting with
man and the financial world will respond the same. We call on people like
Bill Gates to open the funds for development. We know other people who
are sitting there and this is the time you wanted to bring vaccinations and
now KF technology is at the disposal of man for cancer.

02:03:57 K:
We know of the funds of Bill Gates in the Netherlands. We know of them;
we talk to them. Open it up for humanity and there will be no cancer, if you
are the true man of your word. We know other people that are serving the
same and we ask you to open your wealth to humanity, not to KF. Allow
these technologies to open up rapidly so that we get rid of the cancer of
financial control. The healthy man does not need any health care. On the
other hand we see nations' leaders controlling the pharmaceuticals for the
control of nations. Many of these are the kingships. In the countries where
there are kings we see they control the pharmaceuticals to their benefits. We
call the end of kingships. The man has to be free from the cancer of
kingship. All men are equal. Our wish is our command and we shall see the
end of the kingships very, very soon across Europe and the rest of the world.
this is the wish of the supporters of the KF and it shall be done. We
challenge the richest men in the world to open their wealth to serve
humanity through KF and other organizations who work as KF does and not
to benefit themselves on the front end and be charitable in the back.

02:05:31 K:
I invite a very simple man to explain to you. I have known him for nearly 4
years. He has risked everything in his life. Do you remember that I told you
the American government wanted to stop the process with Tepco? They put
his wife and 4 year old child in prison to stop the process. It was his wife
and children and the American government did this to block Tepco. So he
has received everything that we have through; he has been through it too.
KF Japan (KFJ) can you take over and please go through all the pages of
every paper one by one.

KFJ: thank you can you hear me well?

K: yes, good afternoon; you have the total freedom and I would like you to
share the knowledge on the first clinic trial to show the material is used

49
scientifically as non-toxic. Then I would like you to present the second
paper that shows the material for its application to cancer and thirdly go
ahead and close with the third test and results on the mice that you have.
These papers will be free on the KF Blueprint website for governments to go
very rapidly. It shortens the application very rapidly. We thank sincerely the
chancellor at Tokyo University and the professors who helped with this. If
you are Japanese send your thank you letters and commissions to the
chancellor of Tokyo University. He and especially the professors have been
elemental in the background who have helped us do this job. Sometimes the
chancellors dont see the reality because of the position of the power. Pray
for his soul that we extend this research into Fukushima and that area. No
nation needs cancer research and this development more than Japan at the
moment because of the large number of cancers that have come across due
to Fukushima. If you are Japanese send your thanks and letters to the
University chancellor. If you are from anywhere from any part of the world
and you have respect for the work of the foundation do the same. It is very
easy; send your gratitude to the University of Tokyo for what you release as
the Blueprint for Cancer today. Without them this would not be possible
and thank the government of Japan in knowing openly we were researching
who allowed the research to be carried on so they could see the benefit for
the nation. KFJ the floor is yours. Thank you very much for four years of
work.

KFJ: thank you sir, None of this could be issued without your support and
mostly emotional and also financial. The technology is yours. We just find
new ways to use it. So I would like to thank the University of Tokyo and the
professors and assistance who tried their best under stressful conditions to
carry on this research. So, none of this could have been achieved without
your support. Anyway I am still trying to recover from Dr. Rodrigos photos
and his presentation.
K: everytime I share this presentation with KFJ he says he is going sick; the
photos are sickening that Dr R presented. But at least a mother is there for
her child. That is the beauty of it. I leave it to you; start your presentation
please.

KFJ: Can you see these?

K: yes we see the medical and biological uses of CO2 & Copper GANS.

KFJ: I started with water purification before the cancer research almost two
years ago. so I started manufacturing copper gans to purify contaminated

50
water, mostly lake water or any water to turn into drinking water. My
application was focused on Africa and you know the situation. I was trying
to find a cheap way to achieve decent, drinkable water for the people there.
I started doing this copper GANS.

K: can you first tell us your background and who you are? This is our
tradition.
KFJ: Okay. Right now I am in Japan and I and my family spend most of my
time in Japan. We are not Japanese and we came to Japan because of
government pressure we left behind. I grew up here and got a scholarship
from the University of Tokyo which is one of the best universities in the
world. I graduated in chemical engineering with very high honors. Then my
business was with a trading company in Japan. I did that for a long time. I
was in trading all over the world including Europe. I was selling chemicals
and anything you might expect from the trading companies. I was making
lots of money. Tepco was one of our customers and is one of the biggest
major trading hubs in Japan. And the Japanese government was one of our
customers. The Japanese dont come to your company and buy things,
especially overseas. They use intermediary companies called trading
companies. If there is not a company in Japan then they use trading
companies. The institution or the customer or the other give purchase orders
to the trading companies who contact the manufacturers. Then they get a
commission for this business arrangement. I was working for a trading
company. Tepco was our customer. Tepco was a government entity and
after the incident happened (Fukushima) they needed pipes, robotic systems
and more. One of them was my main responsibility was to supply ionization
methods for Tepco. I was shopping all over the world for ionization
methods that might work to decontaminate Fukushima. I encountered Mr
Keshe on the web and his technology and I was very skeptical. I wanted to
give it a try. The difference is the feeling that I was dragged by Tepco to
Mr Keshe so somehow I could have his technology supplied with samples.
This is the part I still cannot understand and is still a dilemma for me. Did I
find this directly or was I directed by Tepco to go to Mr. Keshe and get some
samples. This is a different situation and because the computers and search
engines and everything can be attacked. It is unlikely when you write
ionization exchange on the web the first thing you come to was Mr. Keshe
on my work computer. But when I would go home and enter ionization on
my computer what I encountered was a different thing. So, it was something
like fishing I thought. I realized that after a long time.

51
KFJ: I happened to know Mr. Keshe with the ionization and the rest you
know. It became a different situation in the end. But Tepco got what they
wanted, they got all the information and they used it very well without
giving Mr. Keshe the credibility (acknowledgement) of what he did. The
past is past. Fukushima is more or less safe and people are moving to
Fukushima. Can you imagine moving after Chernobyl? Everybody knows
of Chernobyl in Russia. Tepco was worse than Chernobyl. So now after 4
to 5 years the people who used to live there are moving back. So what kind
of technology achieved this normally on Earth? None of the companies in
their literature have any such technology existing. It was decontamination
on a massive scale for soil, water and whatever you got. I still believe that
Tepco is still using Mr. Keshes technology. Maybe they took it further not
only trying different kinds of gans. They have lots of scientists. They can
achieve many things. Lets stop the Tepco issue for the moment.

KFJ: Mr. Keshe is this enough information?

K: no problem; I just wanted you to give your background and that you were
qualified to do these tests.
KFJ: I still think Tepco should pay.
K: in time this will change; dont worry. Can you carry on with your
presentation please?

KFJ: this is how I started working on cancer. This water is lake water from
a small pond in Tokyo. I made the copper gans and there is regular water.
You can see the copper gans powder in the mixture. It was mixed with
water and filter. When you filter this, the powder of the gans remains in the
filter. The beauty of it is that you can reuse the gans. You have energized or
gans water and you put a few drops of this copper gans water into the
contaminated water and mix it and wait for 6 hours and you see the color
change. You wait for another 6 hours and you see this color change. When
you wait for 24 hours you see the drinkable water. You start with
contaminated water and you end up with this drinkable water. The powder
(gans) can be used many times and this is the cheapest way to decontaminate
the water. I was very amazed with the results and these are the results
(2.20.36). At the lab we did the testing and this is what we get so it was
proven scientifically. The contaminated water became drinkable water.

KFJ: I wanted to focus on the medical uses of gans and I wondered what
could be done with this. But when I started this and we made these products
and they were all made we got a lot of criticism on the internet. It was

52
awful. They were saying the gans was poisonous and you will die if you eat
or drink this. By mistake I had this in my refrigerator and my wife used this
and she and my child consumed it without my knowledge. Everything is
fine. We had to prove the criticism with the orthodox methods and we had
to sacrifice many animals to do that. This is the CO2 gans and this is how
you make it.

KFJ: I see the internet says it is unstable. This is unlikely in Japan, so

hopefully I am not hacked.

K: Just carry on; no problem. If you go to KF website you will see that we
have a method that we show for making CO2. This is the method being
done in Tokyo and this is how KFJ does this. You are all familiar with this
process and this is how KFJ does this. The results KFJ gets with the
technology is using the production of CO2 this way.

KFJ: We try to get the higher yield. This is more or less the same and
everyone can follow the same way. We keep the solution at 60 degrees C.
In a day we get plenty of gans with this method. In order to get a
pharmaceutical grade look at #7 on the chart. There are a few extra steps to
get pharmaceutical grade. What we did when we made the gans you collect
the water and gans is in the bottom of the plastic container. Mix the gans
from the bottom of the container and centrifuge it for 10000 RPM for 10
minutes. In the end you replace the water with MilliQ which is used in the
pharmaceutical (research) instead of water. You centrifuge to separate what
is inside. When you centrifuge the contents of the plastic container with the

53
MilliQ you separate it. You dont see anything on the upper side but you
have the powder. You get the water out and the salt out and all sorts of stuff.
It is like a washing. You fill it up with water and you use Son-K
(sonification?). They use that mostly to mix salad dressing. It is the
surfactant that mixes the water and the oil in dressing. #9 on the chart shows
you the parameters you can apply. What you do is that you repeat the
centrifuge 4 times; it is a washing. #8 shows that you sonicate it again
with the same amount of MilliQ. You can do as many times as you like, but
4 times is enough. In the end you have the very pure gans powder. We
dried the gans powder at 80 degrees C. When you dry it you get clumps.
You can grind it and according to Mr. Keshe you use plastic and not metals
to grind it. You can use a plastic grinder for your application. We used a
special drying to get all the air out. This is how pharmaceuticals are made.
Steps 8 through 12 followed the pharmaceutical way and I dont know that
you need to do it this way. Everybody can do it this way. If you follow this
recipe you can replicate it and get what we achieved. This is for the Gans
powder.

KFJ: the particle sizes of the gans powder vary a lot. If you are going to get
this absorbed in the intestines it has to be nano sized. Further, we had to
make a nano particle gans of CO2 and ZnO. Here is just prepared the
process on the chart for CO2. You can use exactly the same way to make the
nano particles of the zinc. 1-9 is the process for the powder. You dont dry
the powder for the ZnO. When you are finished with the washing you filter
with ashless 8 to 10 micron filter. This gets the bigger particles out (step 10)
and you discard them. There is something called ultra filtration membrane
used in osmotic equipment and you filter. Then you have the particle size of
less than 100 nano in the water. Depending on the quality of the mesh,
sometimes it is very sharp and you get less than 100 nano. Sometimes you
can get 200 nano depending on the quality of mesh that used. We can get
160 to 180 nano. This is used for mostly creating nano particles that we use
in our replication. We used the CO2 nano particles mostly. This is nano
size that is easy to be absorbed or injected.

54
KFJ: after the water purification we wanted to do experiments in the lab.
This is a very basic test to see if gans works on damage to human DNA.
This is called a collect assay that is a very basic test done by the laboratories.
The lights that you see are the mitochondria of the DNA. Mitochondria are
like the cell of the DNA. The lights you see that look like comets are the
DNA and mitochondria is intact in this first picture. There is no hydrogen
peroxide, H2O2, which is a chemical that destroys DNA and kills it. You
see in the 2nd photo on the right that the DNA is wasted by the H2O2. When
you mix the healthy DNA with the H2O2 you get the destroyed and wasted
DNA. It is almost dead. What we did on the 3rd photo on the lower left we
added CO2 Gans water. You use the gans water which is the clear water.
The powder of the CO2 was mixed with water and then filtered. We mixed
the DNA with the gans water with CO2 Gans Water, and after that we added
the H2O2. This time H2O2 had no effect on the DNA. The DNA was intact
and this is very interesting. This was the beginning of everything at the
University of Tokyo when they saw this test. They could not believe what
was happening by adding regular water (CO2) and the H2O2 did not
damage and waste the DNA as you see in the photo on the upper right. The
DNA was intact. This is how all the testing started.

KFJ:

55
KFJ: I got 2 mice from a colleague and we induce a tumor on the mouse on
the left. Its a big tumor. It was a big tumor as you can see the comparison
the coin picture of the 100 Japanese Yen. We were manufacturing the gans
water and we had a lot of it and we wanted to try it. After the injections this
showed it worked for cancer. This was done in 2015. I injected this right
into the tumor for almost a month. This tumor was under the skin of the
mouse and wasnt destructive of the other skin. When the tumor was gone
the mouse was back to normal. This test did not have a control group so it
was not scientifically okay.

56
We saw that the CO2 gans worked for cancer and this was done in 2015. I
injected the CO2 into the tumor for a month. This tumor was under the skin
of the mouth and wasnt destructive to the other skin. Then the tumor was
gone the mouse was like a healthy mouse. This is the first experiment I did
myself that led to the bigger experiments. In order to prove this works we
had to implement some orthodox ways, the regular scientific ways which all
of them actually requires us to use the animals, especially mice. In order to
do the toxicity tests, we followed the regular testing process with 65 mice to
prove the CO2 gans was not toxic. I put all the information on the
presentation as notes. If this is being recorded, if you want to replicate the
experiment all the information is on this presentation and you can replicate
this and see the results for yourself. Once there is criticism at least we have
scientific evidence on the scientific base and we can stop all the unbased
criticism.

KFJ: We used 65 mice and divided them in 13 groups of 5 mice in each

group. We used CO2 gans and CO2 particles were less than 100 nano. The
average particle size was 25 nano. We injected all the mice except for 5 and
injected all with the gans from 1,400 to .5 mg per kilo. We injected the mice
through the vein in the tail. That was the experiment that was done. We had
to sacrifice some of the mice after one day, three days, and sixteen days to
see if there was accumulation or damage to the tissues.

The is called the LD50 estimation to define the toxicity. According to the
test, the toxicity level for the mice at 1,400 mg per kilo is a lot. We didnt
carry further tests because at any standards this 1,400 mg per kilo means it

57
was non toxic. We didnt see any need to carry this further to 2000, 5000 or
10,000. There was no need to waste the lives of any more animals. We
stopped at 1,400 mg for the non-toxicity.

The blood kinetics test is that once we injected the nano particle gans we
wanted to see what happened with the blood. The concentration of the gans
nano particles in the blood goes high and then vanishes rapidly within an
hour. What this means is that the gans nano particles in the blood go into the
tissues.

58
We show gans on the tissues on the liver, kidney and spleen of the mice that
were sacrificed to measure the gans inside the liver, kidney and spleen. We
had to measure how much gans was inside the tissues. This is the test and it
looks like the gans is not accumulated in the tissues. It either goes through
the urine or feces of the mouse. In one hour you lose all the gans that was
injected. Everything stays in the bladder and that means it was neither in the
blood or the tissues and there was no accumulation of this and it was rapidly
discarded. When you look at the photos these are the particle examinations
are from days 1 to 16 to see if there was any tissue damage and none was
observed. We did not see damage to the tissues. These are the photos of the
tissues.

Once we injected the gans and the nano particles we expected some kind of
damage as you would see with other elements injected. This was the control
group. With the scientific eye when you look at the photos there is no
damage in any of the tissues from days 1 through 16 with different mice
sacrificed. According to the conclusion the toxicity for mice is greater than
1,400mg/kg by injection.

59
This means the gans is non-toxic. It did not damage the tissues and it is not
stored in the body. It is rapidly discarded. This was Experiment 1 done in
November-December, 2016 to prove the non-toxicity of the gans. So after
that we switched to the cancer efficacy of CO2 and ZnO.

K: Let me stop you for a second. This is clinical phase one.

KFJ: this is the toxicity to get this clinical phase one.
K: Now you are presenting the cancer cell trial.
KFJ: yes, this was non-toxic. We had to determine the non-toxicity for the
cancer experiment. Most cancer treatment done on the cells are done with
chemo therapy and they are toxic chemicals. We had to follow the rules that
they elevate the chemicals used in chemo therapy.

K: can I ask you a very stupid question? If pharmaceutical companies

receive certification with high toxicity levels how do they get certification?
KFJ: they have to adjust and dilute it.
K: so the amount is diluted to reduce the toxicity?
KFJ: yes. To test the cancer cell and they have toxicity it is okay with the
pharmaceuticals till they get to the root. Mercury and arsenic are very toxic
and kill everything around them quickly so there is no way to get approval
for these kinds of chemicals. Everybody knows these are very toxic.

K: so can we make a conclusion on the paper on the first trial? Please go

back to it. We have proven that the CO2 is non-toxic.
KFJ: yes.

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K: are there any questions from the panel? Do any of the governmental or
scientific people in the background want to ask any questions? Do you see
any questions in the background? The webmasters will tell us.

Rick: what is MilliQ?

KFJ: if you Google it you will see that MilliQ is a water substitute 1 to use in
the experiments instead of water. You have to use this water for the
centrifuge. This is just a brand name. To be scientific you use MilliQ but
you can use regular water as well.
K: may I ask a question? According to scientific and FDA they tell us that
hot water can be replaced by CO2 plasma water which is much more
effective. They told us when we had a meeting with them that they preferred
to use CO2 gans water over anything else because it is that effective.

KFJ: yes, it is effective. We had a lot of criticism that the CO2 was toxic.
Mr. Keshe: yes, scare mongering is a way of controlling things and we saw a
lot of this. We see where it comes from. Now this is the paper done in
Tokyo University to analyze this. If you follow the same procedures you
should get the same results and this shows to us that CO2 is non-toxic to the
organs of the animals. This was crucial in order for us to do the second
trials.

Rick: are stone grinders or bowls useful instead of plastic? And another
question on filtering: Could Clensui micro fiber water filters be used? These
filters are used in household water filters and tech hospitals as well.
KFJ: yes, if you go to 100 nano or 200 nano you can use it. Anything you
get under the nano you are free to use it. We preferred to use the mesh we
had in the lab. Anything that can process 100 nano, you are free to use it.

Rick: what about grinding with a stone grinder?

KFJ: Usually in the lab and pharmaceuticals we use metal grinders for
different chemicals and pills. Mr. Keshe said not to use any metal when
grinding.
Rick: so people could use a mortar and pestle.

1
https://en.wikipedia.org/wiki/Milli-Q --Milli-Q is a trademark created by Millipore Corporation to
describe 'ultrapure' water of "Type 1", as defined by various authorities (e.g. ISO 3696), as well as their ...

61
KFJ: Yes. I did that because Mr. Keshe advised me not to use any metal
when grinding. So we had a glass mortar. I used that. I think Mr. Keshe
knows the interaction of the gans powder and the other metals.

K: are we within the time limit?

Rick: we are 3 hours and there is a suggestion for a 5 minute break so we
can start with the restart before the 4 hour mark.
K: keep the videos going and we will take a 5 minute break.
Rick: Facebook is the only thing that has to restart.
K: we will come back in 5 minutes with phase 2. We will be back in 5
minutes. We will go into the animal clinical trials that are correct for cancer.
5 minute break.

K: we have a number of the audience outside; we are in the Austria KF

center as we were last week. We have a number of scientists, doctors and KF
followers who are here to see. Would you like to start again? Let us start
with the paper number 2.

KFJ: after we determined the toxicity (non-toxicity of the CO2 gans) we

switched to the anti-cancer efficacy of CO2 and ZnO. These nano particles
were manufactured according to the method that I described before. The
gans in the water is nanocized.
K: did you use the gans itself or just the gans water on its own for this trial?
KFJ: I used the gans water. In order to use gans it has to be dispersed in the
water to retain the nano particle.

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K: you are speaking about nano particles and we are speaking about the gans
which are made of the environmental condition and not as the matter state;
there is a big difference. Ok, carry on. This is paper number 2, the Anti-
Cancer Efficacy of CO2 and ZnO, Gans Nanoparticles in Vitro. .

KFJ: yes. The test method we used on human cancer cell tissue. We
elevated three types of cancer as you see in the page above. The equipment
and reagents are written in detail on this paper so you can replicate and get
the same results scientifically. I wont go through this page step by step but
you can replicate from following this page. The test material was GANS
nano particles and Amino CH3 containing water. This was CO2 and ZnO
and we used these particles in difference dilutions in purified water. We
tried four different materials: ZnO and CO2 nano particles were placed
either in water or in Amino which is CH3 containing water. This is totally
different. In general when you add Amino-CH3 it really energizes all the
cells including the cancer cells. So when you have a very strong cancer cell
you know that gans is not working for some reason. This is how we
elevated. Before we started the experiment we werent warned of this effect
of the Amino-CH3 containing water. Mr. Keshe advised us to use Amino
water instead of water and we were expecting to get the higher efficiency of
the cancer treatment. When you add Amino-CH3 the cancer cells also get
energized. This was unexpected for me with the results that I got. We used
that water hoping for a better yield for the cancer treatment but it was
actually the opposite. In that case you can probably use the Amino-CH3
water for something else like energizing your immune system. It could be
used for different kinds of illnesses. We tried it with cancer and it didnt
work.

K: what do you mean that it didnt work?

KFJ: it energized the cancer cells.
K: do you mean the Amino or the water of the CH3.
KFJ: I mean the water of the CH3.
K: you used the water of the CH3 from the systems you built yourself?
KFJ: yes, sir.
K: the Amino becomes effective?
KFJ: no the cancer cells get too powerful by absorbing the Amino.
K: so you cannot use the CH3 for the cancer cells?
KFJ: yes, sir. All the cells are getting energized.

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Rick: isnt that what you have said, Mr. Keshe, not to use the CH3 because it
will tend to increase the cancer?
K: we use the CH3 for feeding.
Rick: right.
K: we use the CH3 as the process of extending the energy. This confirms it.
Rick: in the case of the cancer cell it would feed off that energy like it does
with sugar?
K: yes.
Rick: in certain cases would the cancer be over feeding itself and have a
short life because it blows up in the tests in the lab? Did it just keep
proliferating or did it just blow up and die?
KFJ: it didnt grow fast and die. It is very much protected against the nano
particles. What I guessed was that it was the GANS nano particles that
destabilize the lizozomes of the cells. The lizozomes of the cells are the
toxic. Lizozomes contain the toxic waste or rubbish in the cell. The cell
does not discard toxic material outside. The cells tend to keep the rubbish
inside the lizozomes like the rubbish bag. I believe that the membranes of
the lizozomes burst out and the toxic materials inside the lizozomes are
released and kill the cancer cell. So these nano particles work the same way.
They dont go to the healthy tissues. Instead selectively they go to the
cancer cells. Its almost like a human and they want to kill this. They are
not going to the DNA of the cancer cells because the DNA of the cancer cell
cannot replicate itself. It is easy. Its a marvelous way to totally destroy a
cancer cell. This is the best way! You kill the cancer cell inside with its own
toxic waste. There is no way for it to escape from that.

K: this is done with the CO2?

KFJ: yes this is done with the CO2 and I think
Rick: are you saying that you did separate tests with just the CO2 gans and
then another test with the CH3? Or did you just use the CH3 water for the
whole test.
KFJ: I did it with the water and the CH3 water. I will go through the details.
I just wanted to share how it works. We need different equipment to define
how the nano particles find their way into the cells and into the lizozomes.
What is seen under the microscope is that way so this is a theory that we will
have to prove. We are working on this.
K: okay, carry on .

KFJ: the particle analysis that we get is in order to define how the nano
particles are being measured. The nano particles ..

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K: please move your paper up as we cant read the bottom of the page.

KFG: you see the particle sizes of the gans of CO2 and ZnO and all the
information is written for the scientists to replicate.

We did the cell culture and exposure with GANS CO2 and ZnO nano
particles. These are mainly done scientifically and what I can say is that we
used 3 different concentrations of the gans that was 5 mg. 10mg and 15mg
of the CO2 NP gans and 0.025mg, 0.050mg and 0.1mg of the ZnO NP gans.
These were either in the amino water or the purified water. There were 2

65
different mediums that they were dispersed in. This is the cell viability and
this is the main assay to determine the assay and how we created the data.
This was to express the data.

This is the analysis for when the cancer cells die. We know we killed them
from inside and when the cancer cell started to die there are certain
chemicals that are synthesized in the cancer cells. Those chemicals are
released in the blood. When you take the blood (and see the chemicals) you
know the cancer cells are dying. To determine the amount of cancer cells
you can measure the blood.

K: this is what you call the markets.

KFJ: yes, the markers. So those are various markers. Here is another assay
Mr. Keshe paid for:

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This is mainly done for the research. The DNA ladder assay is a
photographic assay. You get the DNA of the cancer cell and see if it is
interactive or not. It is an assay similar to the mitochondria of the DNA is
showed you before. Also there are oxidative parameters. When a cancer
cell dies it produces oxidative chemicals. You can determine the status of
the cancer cells and patient according to the amount of these in the blood. It
works the same with the animals.

67
The following is more detail in order to express the cancer parameters. I will
go through the markers and protein assay later.

Now we go to the results:

This is the hydrodynamic particle analysis and the CO2 particles were less
than 100nm (hydrodynamic size). Following is more information on the
results:

68
69
KFJ: the graph above is talking about the selective killing of cancer cells by
GANS ZnO. What is says is that there are tissues that were subjected to the
ZnO particles for 24 hours. After 24 hours we measured the cell viability
meaning how many cells were dying or surviving considering the cancer
cells. The orange is the control group and then we show the different
concentrations used to determine the efficacy of the treatment. The last is
used for comparison. What I will share that the amount recommended is 0.1
mg per ml and that works the best. With the amino water it was almost
intact. The ZnO is diluted with amino water. The yellow contained only
ZnO and water and you get almost 100% efficacy. This is for the ZnO. The
next graph is for the CO2 GANS NP.

70
The CO2 diluted in the Amino does not have much efficacy. On the other
side the CO2 diluted in the water is the greatest efficacy. You can replicate
these same things.

The graph above is again the CO2 and ZnO NPs in the human cancer cells.
We do the PRC analysis to determine the levels of the genes with 4 different
parameters. Again a control group was used and that is the orange. When
you use CO2 and ZnO diluted with water we had the greatest efficacy. On
the other side when it was diluted with Amino it was not much different than

71
the control group. As far as you can see the graphs the ZnO had just a little
higher than the efficacy of the CO2. It is pretty negligible when you
compare it to the control group.

The next graph shows the anti-cancer efficacy of CO2 and ZnO GANS NP
in Vitro.

The graph below shows the PCR analysis. When we used the amino in the
GANS it was not effective against the cancer cells. When you used the
GANS in water it was effective.

72
The graph below shows the shared expression of protein levels of apoptotic
genes in human liver cancer cells.

This graph continues for the P53.

73
The data on this shows the consistency.

This following is the last graph:

This graph is consistent with all the other data.

74
We didnt care to put this data on the graph. This is the DNA fragmentation
which means when you add the poisonous chemical to any cell the DNA is
disturbed. You can see the control group shows the cancer is intact and the
DNA is protected. Once you add the GANS ZnO the DNA looks like it is
falling apart. The ZnO and Amino dont affect the DNA and the cancer
looks protected. With the CO2 the DNA starts to fall apart.

This is consistent with the other data we presented.

The ROS and MDA are showing oxidant levels. When the cancer cell is
dying it releases these chemicals that are high in the cancer patient. After
chemo therapy the cancer tests are to measure the dying of cancer cells and
the measuring of the antioxidant levels in the patient. As we see and we
would expect the levels much higher in the control and this is consistent.
The ZnO is a little higher in efficacy than the CO2. The cancer cells were
much healthier when you added the Amino water to the GANS. These are
indicators and are consistent with the data of what we performed before.

75
The following shows the consistency with the data.

76
The conclusion discusses using the cancer cells and cancer tissue. There
was no toxicity to the body but only to the cancer cells by the CO2 and ZnO
GANS NP.

This is only done to the level of the pharmaceutical companies. This is the
basic research. If you go to the human trials there will be more tests. Phase
3 is putting this in Vivo.

What is done after that level will have preliminary tests. This was done on
the cellular level. The whole living organism will be worked on. This

77
mouse purposely has 2 cancer tumors. I injected the NP GANS into the
tumors daily at 0.1 ml per day for 20 days. As you see there is no trace of
tumor that is left. After we see that we were encouraged to go to the second
step where we used the mice.

K: thank you very much. What you see in the pictures on the left side is
when the animal was injected and had 2 tumors and in 20 days there were no
tumors.
KFJ: yes.
K: may I ask you a question regarding our understanding. This phase of
testing allows the 3rd phase to come in to be operational. What are the
chances usually in the normal pharmaceutical condition that you can go from
this phase of the animal tests you can go for rapid results? Usually if you
were doing this with other cancer cells with other products how long would
this take?
KFJ: 3 years or so.
K: so because of the efficiency of this material we can see that the testing
can be reduced? This is a breakthrough.

KFJ: this acts like chemo therapy. I used the same process that was used to
develop chemo therapy agents. This has gone much faster. The toxicity
testing takes a long time. It normally takes 2 to 3 years to determine the
toxicity levels and adjust so that you dont kill the human and you only kill
the cancer. After you determine that the human trials start. It is a long, long
trial.
K: the two phases that we have seen, if this was for a pharmaceutical with
the chemicals, how long does it take?
KFJ: it takes 3 to 4 years.
K: so when it takes 3 to 4 years to see these kinds of results this was done in
the matter of 2 to 3 months from phase one to now. So in a way it is an
effective way and especially for the government officials sitting in the
background, this can be done in any university structure or any structure in
any country, especially in the 3rd world. It can be done very rapidly and at
low cost. This is the beauty of it.
KFJ: the chemo therapy agents themselves are not easy to adjust. There are
stability issues and there are interactions with the other chemicals that are
injected. It is a huge project. The beauty of the ganses is they dont react
with anything and is non-toxic. Even the herbs are toxic up to some level, if
it is tumeric or green tea extract or whatever. Even they are toxic. But this
is not toxic and it makes everything much easier and much faster.

78
K: so we shouldnt see any side effects in this way as we see with the
present pharmaceutical situations?
KFJ: no. You know the story; my wife made a soup out of the gans water
(by mistake) and my kid ate it with no side effects.
K: if people dont know the story KFJ had some bottles of this as drinking
water and his wife made soup out of it. We are talking about a fair amount
of it and he had a fair amount of it. KFJ called me and said Mr. Keshe
somebody put fish in this and they all drank it.
KFJ: the funny thing is my son is 6 years old and after he had the soup he
grew a huge interest in the planets.

K: he became part of the planetary system.

KFJ: Now he is asking me about satellites and all sorts of things.
K: the important thing is that you cannot overdose yourself and the body
only takes what it needs.
KFJ: probably if you ate kilos of the powder you might clog your intestines
but there is no toxicity in this.

Rick: We had a question about that because you mentioned about mg. a
couple of pages back. It said micrograms but you said milligrams. There is
question.
K: it is micrograms; I noticed that.
Rick: so it was micrograms per millimeter.

K: You have done a beautiful presentation on the effectiveness and the speed
of the technology. We had such a breakthrough a few years ago when the
scientists at US FDA were using one system and they moved into _______
(3.39.32) blood. They killed and destroyed a lot of animals to speed up 5
years because of the level of energy in that blood which is blue blood.
That is not royal family blood by the way. It is just happened to be that
kind of blood. So I hope you know the joke. If you are a true British you
are blue blooded and the people never knew the reason why. When the
Vikings attacked the kingdom from the north, the British were so illiterate
and backwards and they did not even have an arrow to fight the Vikings.
The only thing they could find to do was to paint themselves blue and the
Vikings had never seen blue people screaming at them and the Vikings used
to run away. So they say if you are a true blueblood you are of the ones
who painted themselves. Now we find the solution in another way.

79
K: The beauty of this is that it reduces a lot of expenditure and time. From
this point on you will see pressure from the pharmaceuticals. The pressure
is on the pharmaceuticals not on us. Now different materials can be mixed
with CO2 and ZnO. We go into the level of new materials in which ganses
can be used without creating any side effects. We know a number of
researchers that are going around with a number of governments which by
use of the gans water they are literally cutting around any side effects of
medicine. This is not just what we see here. The implication of CO2 gans
water itself will revolutionize the world of medicine and the
pharmaceuticals. It costs literally nothing and you can produce it
unconditionally and reprocess it.

K: The implication of this anti-cancer test in these two papers will become
historical papers. These papers will be the backbone of the future of
pharmaceuticals because it changes everything. This is why we said if you
are in the background, we put this on the website. Deliver this to every
pharmaceutical company and to everyone you know. Its no use for others
trying to bypass or take over because they are not aware of it. It gives
validity to the science to be publicly used. The beauty of what you have
seen these past few hours is that no organization has ever shared knowledge
so freely. This is trillions of dollars of research there at your fingertips. We
are not afraid of it being stolen; we are proud to make a gift of it and this is
the beauty of the foundation.

K: if this speeds up development of other materialsand we have seen the

effectiveness of it with Dr. Rodrigos presentationthis can save a lot of
lives. As I said the parents who grieve for their children and the children
who lose their parents can be remedied by this and brought to the market.
We will go into the 3rd Paper which we have curtailed. It has been stopped
because whatever we wanted to achieve has been achieved. I saw the results
last week and I asked that the final paper be written. It is no use carrying on
any further. The data you are going to see is so effective that there is no
ambiguity. CO2 in the gans condition that we present in paper 3 is the
solution for cancer. There is no doubt and you will see the data. We
challenge any organization to challenge us

K: The beauty of this paper is as you have seen the strength of our
knowledge from the ground up. Everything you have seen including the
machines used on these papers is not unusual. This can be replicated. I
asked the Japanese team to make sure everything is transparent. No

80
organization will ever publish these papers. They go to the back shelves of
the pharmaceuticals and nobody ever sees them so they can continue to
make millions. This is the beauty of what we are doing and the openness
with which we are doing this.

K: I thank Japan and Tokyo University and I ask all of you, and it doesnt
matter how many of you, go to the Tokyo University website and thank
them for the gift of the nano particle that was presented today and supported
by them. Thank the chancellor for his dedicated job with his university in
allowing this to happen because there is more to happen in Tokyo. You will
see; we will go to different dimensions with these papers in Japan. The
beauty of it was that when we asked for this to be presented, nobody
objected for these kinds of papers to go public. They all wanted to be here
to present it. The beauty of this is sharing the knowledge in such a vast way.
We go to the Paper 3 which is the final and it was literally finished
yesterday. The paper was written yesterday and I asked them last week
when we saw the first two animals sacrificed, that was it.

KFJ: we cut the third test in half.

K: we had to do it; it was there with all the data of the trial. He was going
to test other materials. We got the result we were looking for and this is
traditional; when you achieve a result the trial stops. As I said before the
UN ran a trial for HIV. It was done 5 to 10 years ago and was going some
trials in Africa to reduce HIV. The scientific paper is in the background and
they found in the trials that by circumcision of the man they could reduce
AIDS transmission from one to another. And the process was so successful
and they saw the reduction. After 6 months the whole project was stopped
because it (circumcision) became compulsory. It was a subtle change that at
the point of the cut of the skin it created the protection. It is normal that
when you are successful in a trial you stop and you dont go any further.
There is no use trying to find something else when you have found what you
are looking for.

K: the trial Number 3 will be shown and then we invite any questions. Then
we will tell you what we have planned. Would you like to go into the
presentation of the trial on the animals please? Would you like to show the
live animal paper on testing?
KFJ: Yes, sir.
K: let me tell you something that is fantastic: this test has taken just about 3
weeks; it could have taken 10 to 20 years or at the minimum 5 to 10 years

81
for what we have. It shows the beauty and the perfection of the technology.
This is paper 3, Anti Cancer Efficacy of CO2 and ZnO GANS Nano
particles in Vivo. This means it was digestive. You dont need to inject it.
You can take it home; its become like a headache table. If you have a
headache you get the tablet, a few aspirin. Now we need more clarification
by world institutions to examine and to check. Literally the institutions and
individuals who go with this and try it, more or less upon the approval of the
organization, with a lot of people in the system or by themselves, twenty
days is the amount of time you need for getting rid of a tumor. There is a
background on understanding that you have to find the right dosage. We
think we know what the dosage is from testing on the animals.

K: We have a good idea with what we have seen, and the scientific cleanup
has to be done to be precise, the cost of saving a life from cancer with this
technology is less than one Euro when you mass produce it. It is cheaper
than aspirin. The biggest nightmare for man, cancer, it has now become the
biggest joy to live. Listen to this and we will rapidly deliver this technology
in Ghana Atomic as a way of cancer treatment for all of Africa. We leave it
to the individuals for the donation to the Foundation for further
development. We dont put any price on it and it can be done. The beauty
of it is our strength of sharing (which was done) because we know it will
change the course of humanity. But the biggest problem is that I have
developed another problem for mankind with this.

K: Millions and millions of people die every year of cancer. That is why the
7 billion become 10 billion much faster. Is there a need for man to go into
space? The beauty of this is that you calculate how many million people
every day die of this and in the short time to come they will not die. The
population explosion will be a reality in a hundred years. It will go beyond
and this is one of the reasons on the other hand that we can use this
technology in space so that you can survive for hundreds of years in deep
space without actually worrying now that the biggest problem is solved. A
dedicated man in Japan has changed the course for humanity. Go ahead
please.

KFJ: thank you sir, none of this was possible without your support, your
invention and you financial support. So what we have achieved here is
actually yours, sir.
K: Go ahead, please.
KFJ: Yes, sir.

82
K: while he is trying to share his screen I will let you know something new
about KF. From next term sometime in May as you know we have the
Wednesday morning Agriculture teachings and on Wednesday afternoons
we have the doctors teaching. From next term we will add Monday
morning from 10 to 1 as part of Scientific Paper deliveries and we will bring
scientists whose methods can be part of KF or that have been independently
silenced by science for whatever reasons. We give the world scientists a
platform to release and discuss their technologies. Maybe some will be
beneficial to us and maybe some will not be beneficial to us. But it will be
beneficial to those who might use it.

K: so, in the coming weeks we add a 4th special class for the scientists and
you have to be a scientists. We dont want to do it any other way, but we
will leave it as open as possible. And in that session we discuss the latest
scientific papers. If you know a scientist whose paper has never seen the
light of day because of whatever reasons, we have another scientist here and
I discussed this with him a couple of days ago. We will put a team and Mr.
Kahn (KFJ) will head the team of other scientists to work and to bring the
work of others to the forefront. And we do it in a way to give them a
chance. In another way we will see their knowledge that will enlighten us.
In the same way as I said, one of the biggest problems for humanity is the
kingship. Now we will have scientists to present what has been cleared out.

K: We will also run a power program on Monday afternoon in the coming

weeks for those who have been imprisoned due to their science and what has
been stolen and for whatever reasons they have been attacked. And we have
seen that to a number of scientists particularly in Belgium where they
imprison the scientists who dont give their (information to) or they kill
them. So if you know scientists who are in that position, bring their works
and we will fight for their freedom. The KF will finance every means to
bring the world scientists who have been imprisoned by mis-justice,
especially by the king of Belgium to steal from humanity. We open this
public support. There are many, many scientists especially in ex-Russia
who are imprisoned. Or there are scientists in other countries, who because
of their work have been imprisoned. We give them a platform and we
search for their freedom.

K: This is our job. We cannot have a nation, as One Nation and KF that we
live in and are building and have men of science and men of integrity
imprisoned by thieves of their science. Because of this especially in

83
Belgium, it will be one of the first nations to end the monarchy because the
monarchy in Belgium is beyond control. There is no monarchy; it is the
terrorism of scientists. And we ask for those that are sitting there and
publicizing and supporting these kinds of behavior. From now on scientists
will be supported and protected by the KF. We are not there and we do not
ask for any riots. We ask for a silent request to allow the scientists to be free
to deliver their work and not have it stolen from them.

K: If I had been imprisoned as was the plan, you would never have seen this
technology; it would have been hidden. The plan was to castrate us, put us
in prison and whatever we do is theirs. As you saw the king of Belgium
came to me begging for me to give him the technology or leave the country.
I left the country. He abdicated. We fight for freedom and at the moment
we have another case in Belgium. They want to put us in prison for giving
our technology freely by a man who has already assassinated many people.
The chief constable of Kortec, Mr. Delanoix, has now come up with a new
approach, that we are terrorists. Scientists have become terrorists while they
(Belgian authorities) terrorize others. We handed this case over to the
International Police and we are working very closely. And, the sessions on
Monday afternoons is to stop these things. If you know scientists or men of
integrity in their beliefs who are in prison KF stands as their supporter. This
is our job. This is where we are. We are free to give our knowledge and we
are free to support the man of freedom. Go ahead please and thank you very
much.

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KFJ: we did the in vivo with the live animals. Actually this experiment was
supposed to be completed by now. It started on February 20, 2017 and it was
supposed to be completed in one month which is my mistake mostly because
the place where we use the lab. It is at the University of Tokyo, and they are
not actually handling the live animals there especially the mice. But most of
the work has been done there. There was an issue and we had to figure out
how to induce cancer in the mice. Anyway they were chemically induced or
we got the tumor to inject into them. It didnt work out and they didnt get
the cancer. We had to figure out how to make the cancer in the mice in 3
weeks. So it got delayed a little bit. We started first with the mice and the
groups in it. With the orally fed mice if we had success we didnt need to
sacrifice the second ones which would have been the ones that were injected
with the nano particles.

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KFJ: we started using the nano gans of CO2 and ZnO and mixed the
particles and fed it to the mice. There were 50 mice and 10 were used as the
control group. The other group consisted of mice with cancer and they were
only fed with CO2 nano particles. The 3rd group of 10 mice with induced
cancer was fed with ZnO nano particles. The 4th and 5th groups would have
been injected with CO2 or CO2 and ZnO. We limited the number of mice
and normally these experiments are done with 15 (50?) mice. Mr. Keshe
was not comfortable with the amount of mice to be sacrificed. This is the
minimum you can get for some sort of significant data. The amount of CO2
to ZnO mixed was 3:13 parts of CO2 and 1 part ZnO.

K: can I interrupt? The reason we used a mixture of CO2 and ZnO is

because the cancer is emotionally dependent. You have to do this. You
cannot just go with CO2. This is what I said from the beginning. We have
to consider that even though we make 100% CO2 there is always some ZnO
in it because of the way you produce it. Carry on please.

KFJ: yes, the CO2 does contain some ZnO. The ZnO stops the reoccurrence
in the future. In the efficacy we didnt mix CO2 and ZnO but did individual
tests. In the individual tests there was no difference. I saw and I thought
that would be good if we could mix the CO2 and ZnO because the ZnO also
has some kind of property that stops the reoccurrence of the cancer cells.
The other side of the ZnO is more on the cellular base and more toxic than
CO2. It is 100 times more toxic than CO2 as a material. If you use ZnO
gans water, that is not the case. But what we are dealing with here is

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serious, terminal cases and tumors are almost 1/10th of the body surface.
The gans water would probably work as well and you wouldnt have to
worry about the toxicity of ZnO or CuO.

K: the thing is we prefer to use CO2 with the water of the ZnO of the nano
particles. You have the security of no heavy particles in the body.
KFJ: yes, ZnO is actually the nano particles. So we found a way eventually
how to produce the cancer in the mice that is in the report.

KFJ: the parameters here are 3 grams of CO2 or ZnO gans and they are used
in different combinations. I used 3 parts of CO2 and one part of ZnO. I
mixed 3 grams of CO2/ZnO powder into 1 liter of pure distilled water.

K: One liter? So you mixed how much again?

KFJ: yes, one liter. I mixed 3 grams of CO2 powder for 1 liter of water. Or
you can use 0.227 or 0.5 grams of CO2 and 0.75 grams of ZnO. When you
get the solution you get 0.3mg per ml.
K: can I refer and go back to this? This is what you learned from the
experiments at Tepco?

KFJ: no, not actually.

K: they used the dry material.
KFJ: yes they did but they did not disclose how much they used in each part.
K: but this is better than knowing how they used it.

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KFJ: yes, maybe they will disclose that we follow the same method. They
mixed with the water and they fed the mice with the water one by one every
day and this is the same method we followed. There were 50 mice with 10
in each group. There is a control group of 10 with cancer. Right now we are
in the 2nd phase and we fed mice with CO2 and we fed mice with CO2 plus
ZnO solution. And before going to the results I will show you the picture
because we dont have enough as we only have 5 that we sacrificed.

40612
You have to sacrifice the animals (3 white mice pictured) to see that there
are no internal tumors. After 20 days the cancer is more healed. When you
sacrifice the animals it looks like this. The blood indicators are not there and
there are no visible tumors. We dont know what is under it. So we have to
sacrifice the animals and prove the cancer is gone. This is why we sacrificed
these animals. This is the original photo of inducing cancer (the mouse on
the left). Then we feed them for 20 days and there are two cases here. The
third photo on the right shows what we get at the end. It is similar to Dr.
Rodrigos treatment especially in this case. This case has healed much
more. These are the photos I can show you. The next page shows there is
not much after the 4th day

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The control group consists of 10 mice and you can see this is 2.27 grams of
tumor. After 20 days feeding 0.3 mg a day of the CO2 you get .
K: you have 2 instead of 20 at the beginning of the 3rd line of information.

KFJ: no, the 2 is for the 2 mice that were sacrificed. There were 10 mice in
the control group. Of the 10 mice there were only 2 that were sacrificed and
cut (to check for tumors).

Mr Keshe: there are no cancer markers in the blood in the 8 in this group>?
KFJ: no markers are in the blood. In order to see there is no cancer we have
to cut the mice and look inside.
K: you sacrificed 2 out of the 10 and there were no blood markers.
KFJ: yes, the rest of the 10 had no blood markers for cancer. We have not
cut them yet.
K: there were no cancer markers in the other 8 of this group.
KFJ: yes, because we have to do .today is the 18th and if I had 2 weeks
K: There is no use killing more when the data is there. Carry on please.

KFJ: Yes. The last part is the group of CO2 and ZnO and it is the same at 20
days and this is the control group. In the control group is the numbers are the
same. There is only one control group. This is the main control group and
the numbers are the same. Out of the 10 mice we fed CO2 and ZnO and we
only sacrificed 3 so far. 7 are still living in the cages. They showed no
markers of cancer. What we confirmed after the sacrifice of the 3 is that

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there are no tumors, no cancer and no side effects. There was 100%
reduction in both cases.
Mr. Keshe: what do you have on your data for the first day of reduction of
tumors and markers?
KFJ: we see them for 3 to 4 days after being fed (CO2, ZnO) we see the
reduction. By 8 days the blood markers for cancer are very low and you can
pick up the cancer. The cancer persists for almost 2 weeks and gets smaller
day by day. You dont get any cancer markers in the blood even though the
see the cancer tumor is big and it is inconsistent.
K: even though there are no markers? And then the tumors reduce (in size).

KFJ: Yes, the data is inconsistent.

K: when is the first day you see reduction?
KFJ: You visibly see the reduction in one week.
K: what about the blood results on the markers? On the report you show
30% reduction after the 2nd or 3rd day.

KFJ: Yes. It depends on the mouse itself. Some mice are more healthy and
eat and drink more and are more lively. Some of the others are not so lively.
Some of the blood markers drop in 3 to 4 days and once mouse didnt show
the marker change until 8 days.
K: what about the 10 in group 1?
KFJ: Eventually in 2 weeks everybody is wrapped up.
K: there are no cancer markers.
KFJ: yes, there are no cancer markers. In the 2 groups it starts 3 to 4 days
and you lose the cancer markers mostly in 8 days. On the contrary when
you see the markers disappearing you see the tumor getting smaller and
shrinking but you still have the cancer. This is inconsistent. The tumor is
getting smaller. You would expect things in the blood and the antioxidant
and protein levels in the blood are inconsistent. The results are there. We
cannot detect the cancer in the blood. But the results are there.

Mr Keshe: so we dont see a need for sacrificing any more animals. But this
is all for intestinal cancer, am I correct?
KFJ: yes.
K: We need other organizations around the world, other universities and
government organizations to come in. Go to the bottom of the KF website
which is set up for www.cancerprocessing.org and join us to share the
burden and give the financial support needed to test this for other organs
such as liver, kidneys, and other tumors. Thank you very much, Tokyo.

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KFJ: thank you very much.

K: the important position for us is now we know we have seen it is 100% no

cancer. So we need this to be done and to be completed because we know
this technology and this CO2 supports the intestinal cancer. This is our
finding. The reason I brought this is I couldnt see for the last week why we
would sacrifice more animals. All of us die; that is normal. As the results
were coming in the last week I asked for the report because there is no need
to go forward and sacrifice any more animals. We injected them, gave them
the cancer, we fed them to get rid of the cancer and we proved 10 out of 10
have no cancer. 5 were sacrificed out of 20 and it confirms no toxicity and
no cancer tumor. We need to take this further and we can do this at KF
Ghana with the research in the Atomic Commission. The reason we brought
this up is for more scientific organizations to joint the KF in collaboration
tests. Of course it will be headed by Mr. Kahn. At KF we are very involved
in this and as you have seen with Dr. Rodrigo it worked with the breast
cancer. If you look at it digestive or environmental works the same. When
you use injections there is a minute amount; when you use digestive it is still
a high proportion. We have done the calculation on the basis of present
understanding and we see this as a blueprint for cancer and for the reversal
of cancer. For human beings we estimate that for 100 kilo body weight it is
800mg which is less than a gram. Am I correct?

KFJ: yes, in human it is more or less converted to a gram.

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K: we have been asked if there is enough for the chancellor of Tokyo
University, the president.
KFJ: there must be.

Mr Keshe: thank Tokyo University for their effort and what they brought to
humanity. And especially if you are Japanese without Tokyo University this
would not have been possible. It is important that we understand and respect
the people who have done the job for the foundation. In any way we can do
we have to go to the next step and finance the next phase for different organs
as part of the results that are not here. This report will be completed in the
next week or so with a lot of detailed information for the doctors to come in
that we see a small amount of gans in the blood stream analysis. This to us
is a very good thing because we inject in gans trials into the blood circle.
But if the gans found the way in then in a way it can deliver the same thing
to the other organs if there is a secondary cancer. That is for the scientists to
do.

Mr Keshe: As far as we can see from the other trials and investigations this
brings us to a close in a way of the foundation work with the blueprint.
This means and thank you very much, Benjamin. This will be in the Ghana
Atomic very soon. I can see Benjamin on the right side (he should be in the
factory but he is at home watching this). What we are going to do if you are
a pharmaceutical we have given you a path. We know many people have
used gans in different forms to overcome cancer. But because of the threats
from what I call the hooligans of the internet they have been pushed not to
publish. We ask you to deliver your findings. We know there are Germans,
Belgians, and Americans who have used the cancer process with the gans.
Now know this is safe and we have seen the work of Dr. Rodrigo. We have
seen this with the scientific; we did the human trials before the animal trials.
That is the way it should be. If humans have it we leave them alone. We
inject them into the animals to see if we can save the human. Those of you
who have cancer, volunteer your life. This is the right way and then we
bless your soul and elevate your soul.

Rick: is there a way to save the lab test animals maybe some of the ones that
are put away?
Mr Keshe: write an email to the Chancellor and say that we would like to
adopt the animals who survived. Why not? We have seen people adopting
dogs after they are not longer hunting dogs. Write to the Chancellor that you
will give them love and care.

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Rick: this lab testing of animals is a world wide phenomenon as well.
K: but they dont know what they are going to get; but this time we know
they have no cancer so they can be given a good life. Please, can someone
find the Tokyo University chancellors email?
Tokyo University ChancellorPresident, Makoto Gonokami, PhD
Dr. Makoto Gonokami gonokami@ap.t.u-tokyo.ac.jp

K: These people have a lot of fear from the others because these things are
not done this way. These are afraid for their position. These things bring
millions of dollars to the university and take 30 to 40 years and a lot of
PhDs. Everything we have done was in less than 6 to 8 months. So, we
should thank a lot of people, especially Mr. Kahn, especially if you knew
what I know that he has gone through for the past two years from Tepco, and
the rest of it. He had to rush from Tokyo to go to California where the
American police incarcerated his child. This is unbelievable, separating a
mother from her child just to pressurize the man while he is away. Tepco
speak to the Japanese about only what we achieve and they dont want
anyone else to know. We are aware of it. So we leave it as that; we
understand a lot of things.

K: So we are seeing that GANS are safe and non-toxic. We are talking
primarily in respect to CO2 and ZnO; they have been tested and are non-
toxic. We do not speak about any other GANS such as copper or anything
else. Please understand, once you have a good working system what is the
use to try something else? Maybe something will work better but the
combination of CO2 and ZnO support both the physicality and emotional
changes. One thing that is not here and you will see it when we go into
more detail is that the mice after 4 or 5 days are running around. Am I
correct?
KFJ: yes, they are having fun.

K: They are having fun. We dont know how much fun, but we will know in
about 20 days. So we try to bring this section of the blueprint and we will
come back every Thursday morning. If you are trying the material as a
scientific organization, report back to the foundation. If you have tested it or
are testing it, please report back to the foundation. We will publish it on this
page and we will need a huge amount of financial support for these kinds of
research that is done by all the people. We know the Ghana Atomic Center
will be built in the next 2 or 3 months. I am back in Ghana in the next few
weeks and then we carry on with the process.

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K: It is important to allow other scientists to share the knowledge with us
and I know that a lot of you know a lot of it. You know scientists whose
work is essential to humanity and it has been shelved. Send it to the same
point at the bottom and then we will find a way to disclose their work or
bring them in to explain themselves. A lot of scientists cannot believe that
they are being given a chance to show their work. They have been silenced
very heavily. It is our job as One Nation to support all our citizens,
scientists and the rest. And, I said at the Rome Conference that my wish is
to see the end of kingship and my wish is for the king of Belgium to be the
first and the rest follow and that this is peaceful with a lot of pray and
respect that we can elevate the soul of the king to put his crown down (to
show) he is equal to the rest of the men and not elevated just because he
carries a gun in his pocket.

K: Thank you very much indeed and we will see you on Thursday and we
will explain the fundamental structure of the body of the man and open
another door into the world of the science. And then you will understand
even how you are constructed without knowing why you have a brain and
what is the function of the brain to start with that starts with the soul of the
man. Thank you for very much indeed for today. Are there any questions in
the background?

Sandy, Universal Council: Mr. Keshe, I would like to thank the doctors and
the researchers for the great gift and let them know that the Universal
Council is giving them their support to them. I just wanted this opportunity
to thank them.

Mr Keshe: thank you very much; please make your link on the KF front
page as usual where the Youtubes are so that people can see this part of the
teaching. Please dont forget to write to Tokyo University and thank him for
what he has given by the University.
Dr. Makoto Gonokami
gonokami@ap.t.u-tokyo.ac.jp

We will come back on Thursday morning. We will carry on with the

research and we need huge amount of financial support. The Ghana center
will be built in the next few months. It is important to allow other scientists
to share the knowledge with us. There are scientists whose work has been
shelves. We will find a way to expose their work. Many scientists have been

94
silenced very heavily. It is my wish to see the end of kingship and the wish
is for the kingdom of Belgium to be the front. Thank you very much and we
will see you on Thursday and we will explain the fundamental structure of
the man. You will understand the function of the brain. Thank you for
today. And thank all the professors that this technology could be tested.
Thank you very much.

KFJ: I want to add something; we did injections but I suggest that people not
knowing. Injecting yourself with GANS, I dont recommend that you need
to do that.
K: I think we will leave it at that because we are going into the feeding.
Please dont do injections.

Rick: there was a question from someone: is it okay to drink the gans or only
the water energized by the gans?
K: Read the paper; that is the easiest way. There is a process in how you
drink water in different ways and it gives you different properties. If you
have people with high blood pressure and high sugar you find out that how
you mix the things together affects in a different way. It is the same water
and the way you do it is what counts. If you are diabetic Benjamin is in the
background and if he is still there he can tell you how to do it. If you have
high blood pressure, using the same water in a slightly different way brings
your blood pressure down and holds it down. It is important on how you
mix it. Thank you very much; bring your brain with you on Thursday and
you might find out how it was made. Thank you very much. Thank you
very much Mr. Kahn.

Rick: that brings to an end the Cancer Blueprint Day for Tuesday April 18,
2017. Thank you everybody for attending and I hope you got something out
of it. I know that it seems like everyone did. This is a big moment for
mankind and perhaps for others in the universe.

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