The emergence of nanobot society
OUTRAGED HUMAN













So, they injected it into the military, police, emergency services.... Now everyone is injected with a device with a "real IP ADDRESS"....






0:00

Thank you very much. So one word of notice before we begin,

0:03

all the technologies that you are going to see here now are real.

0:06

And with that said

0:07

I'd like to first tell you the story about

0:10

this uh... little girl named Dana

0:12

she's very special for me because she's my daugther

0:14

and Dana was born with a leg condition requiring frequent surgeries like this one

0:19

uh... she had when we were in Boston

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and um... I remember taking her to that particular surgery

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and uh...

0:26

I rembember her being admitted and she was excited at first

0:31

and then just before they got into her the OR

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I looked at her and she was... afraid, she was little worried and

0:38

who wouldn't be? Because surgeries today are complicated

0:41

and they're often very risky.

0:42

Now let's imagine a few years into the future, into the near future hopefully,

0:47

Dana will arrive to hospital for her ??? surgery

0:50

and instead of being prepped for anesthesia for the OR

0:54

the surgeon will just take a syringe and inside the syringe

0:58

there are millions of tiny robots, of tiny machines

1:02

that will be injected into Dana's bloodstream.

1:04

They will autonomously locate the place they need to be in,

1:08

they will excite out the injured tissue,

1:11

then will remove dead cells,

1:13

then they will...

1:14

stimulate and guide the regrowth of healthy cells across those tissue gaps,

1:18

they will release drugs that relief pain and reduce inflammation

1:23

and all the while Dana will be sitting on the chair

1:25

eating a sandwich, reading a book, might be the next

1:28

twilight saga book which she'll be able to read because she will be 16 by then

1:32

And...(giggles)

1:33

uh... when these robots

1:35

have completed their job they'll simply disintegrate

1:39

and disappear from her bloodstream the next day.

1:42

So these nanobots have been envisioned in the past 30 years

1:45

by people like Eric Drexler, Robert Freitas and Ray Kuzweil.

1:49

Today I'm going to show you that these robots exist

1:51

here in Israel.

1:54

I'll show you this syringe

1:56

which I've brought from my lab.

1:58

So this syringe has inside it a thousand billion robots.

2:03

So these robots are each fifty nanometers

2:06

long as you can see in this slide under the microscope.

2:11

Fifty nanometers is about 2000 times thinner than the thickness of your hair

2:16

OK? And... umm... These robots were born actually 3 years ago

2:20

in a research I did with Shawn Douglas, now a UCSF Professor.

2:24

But over the past year and a half

2:25

in my group at Bar-Ilan University

2:27

We've been developing and testing robots for a variety of

2:31

medical and therapeutic tasks.

2:33

We've invented ways of making them safe for use

2:37

and non-inmunogenic

2:38

and we learned how to tune their stability in our bloodstream

2:41

to fit either short-term or long-term

2:44

even days long medical procedures.

2:47

So to carry out medical and therapeutic procedures in our body

2:50

with the upmost precision,

2:51

we need to be able to control molecules

2:53

Controlling molecules is a very simple challenge

2:56

in modern scientific knowledge.

2:58

OK? Let's speak for example about the class of molecules we know as drugs

3:02

So despite...

3:04

amazing progress made in the past four decades

3:06

the way we think about drugs and we the way we use drugs

3:09

has been essentially unchanged

3:11

and it's similar as two hundred years ago

3:14

right? You hear about about big pharmaceutical companies

3:17

spending huge amounts of money

3:19

searching for better, safer drugs.

3:22

Attempts that usually fail.

3:24

OK? but,

3:25

searching for let's say a safer cancer drug,

3:28

half it is a concept that has a flaw in it.

3:30

Because searching for a safer cancer drug

3:32

is basically like searching for a gun that kills only bad people

3:36

We don't search for such guns,

3:37

what we do is training soldiers to use that gun properly

3:42

Of course in drugs we can't do this because it seems very hard

3:45

But there are things we can do with drugs

3:47

for example, we can put the drugs

3:49

in particles from which they difuse slowly.

3:51

We can attach a drug to a carrier

3:54

which takes someplace but, this is not real control.

3:57

When we were thinking about control we're thinking about

4:00

processes is the real world around us

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and what happens when we want to control a process

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that's beyond our capabilities as humans

4:08

we just connect this process to a computer

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and let the computer control this process for us.

4:13

OK? So that's what we do.

4:15

But obviously this cannot be done with drugs because

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the drugs are so much smaller than the computers as we know them

4:23

The computer is in fact so much bigger

4:25

it's about a hundred million times bigger that any drug molecule.

4:28

Our nanobots which were in the syringe

4:31

solve this problem because they are in fact

4:34

computers the size of molecules.

4:36

and they can interact with molecules

4:38

and they can control molecules directly,

4:40

so just think about all those

4:42

drugs that have been withdrawn from the market

4:45

for excessive toxicity

4:46

right?

4:47

It doesn't mean that they are not effective,

4:49

they were amazingly effective,

4:51

they were just guns shooting in all directions

4:53

but in the hands of a well-trained soldier

4:56

or a well-programed nanobot

4:58

using all the existing drugs

5:01

we could hypothetically kill almost any disease.

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So we might not need even new drugs.

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We have amazing drugs already,

5:09

we just don't know how to control them, this is the problem

5:11

and our nanobots...

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hopefully solve this problem and I'll show you how.

5:15

So there is an interesting question "how do we build

5:19

a robot or a machine the size of a molecule?"

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so the simple answer would be: we can use molecules

5:25

to build this machine.

5:26

So we're using molecules, but we're not using just any molecule.

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We're using the perfect, most beautiful molecule on earth, at least in my opinion,

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which is DNA.

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And in fact every part of the robot,

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every part of out nanorobots:

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Moving parts, axis, locks, chasis, software,

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everything is made from DNA molecules.

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And the techonology that enables us to do this

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originated thirty years ago when the pioneering works of Nadrian Seeman,

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culminating 7 years ago in the works of Paul Rothemund from Caltech,

5:56

which was also featured in TED,

5:58

and it's called DNA origami.

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Now in DNA origami we do not use a piece of paper,

6:02

we use a single long strand of DNA

6:05

and we fold it into virtually any shape we want.

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For example these shapes, so these are actual microscopic images

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of shapes the size of molecules that were folded from DNA.

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so the smiley you see here in the center of the screen for example

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are a hundred nanometers in size

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and we make billions of them in few... in a single reaction.

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Now since 2006 several researchers, really talented ones,

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have been expanding the limits of the technically feasible in DNA origami

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and now we have an astonishig array of shapes and objects which we can build

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using this technique.

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And these researchers also gave us computer-aided design tools

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that enable everyone

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very very simply to design objects from DNA

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So these CAD tools amazingly

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enable us to focus o n the shape we want

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forgetting the fact that these structures are in fact assemblies of molecules.

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so this is for example a shape the computer can actually turn into DNA molecules.

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and the output of this CAD software, as you can see,

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is a spreadsheet with fragments of DNA

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which you can attach to a message and send to a company

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one of two dozen companies that make DNA by order and you'll get those DNA's

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several days later to your doorstep

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and when you get them all you need to do is just mix them in a certain way

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and these molecular bricks will self-assemble into

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millions of copies of the very structure that you designed using that CAD software

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which is free by the way, you can download it for free.

7:34

So, let's have a look at our nanorobots.

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So, this is how the nanorobots look like, it's built from DNA as you can see

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And it resembles a clam shell in which you can put cargo

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You can load anything you want starting from small molecules, drugs,

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proteines, enzymes, even nano-particles. Virtually any function

7:54

that molecules can carry out, can be loaded into the nanobot

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and the nanobot can be programmed to turn on and off

8:01

these functions at certain places and at certain times

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this is how we control those molecules

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and so this particular nanorobot is in an off state, it's closed,it's securely

8:12

sequestres anything, any payload you put inside

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so it's not accessible to the outside of the robot,

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for example, it cannot engage target cells or target tissues

8:22

But we can program the nanobot to switch to an on state

8:26

based on molecular cues it finds from the environment

8:30

so programming the robot is virtually like assemblying a combination lock

8:34

using disks that recognize digits,

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but of course instead of digits we are assemblying disks that recognize molecules.

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So these robots can turn from off to on and when they do

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any cargo inside is now accessible,

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it can attack target cells or target tissues

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or other robots which you'll see later on.

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And so we have robots that can switch from off to on

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and off again, we can control their kinetics of transition.

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We can control which payload becomes accessible at which time point

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Let's see an example how these robots for example control a cancer drug

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So what you can do is you can take nanobots,

9:14

you can put the nastiest cancer drug you may find

9:17

into the robots, even a cancer drug

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that's been withdrawn because of excessive toxicity

9:23

Ok? When the robot is locked

9:25

and you put them in your mixture of healthy cells and tumor cells

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nothing happens, no cell is affected, because the robot

9:32

safely sequesters those drugs inside.

9:35

When we unlock the robots

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all cells die because the cargo inside the [robot] attacks anything on sight.

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So all cells eventually die. In this case this is a fluorescent molecule

9:46

to help us see better the output.

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But when we program the nanobots to search for tumor cells particulary,

9:53

so only the tumor cells

9:56

uh... only the tumor cells die because

9:59

the robot doesn't care about the bystander cells, about the healthy cells.

10:04

So it does not harm them at all.

10:06

And we have nanorobots in our lab that can target

10:09

about ten types of cancer already and other cell targets

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and my team keeps expanding this range monthly.

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So these are nanorobots and to another topic

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organisms in nature, like bacteria and animals

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have learned very early in evolution that working in a coordinated group

10:29

conveys advantage

10:31

and capabilities beyond those of the individual

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and since we are interested in

10:36

very complex medical procedures, very complex therapeutic settings,

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we're wondering what we could do

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if we could engineer artificial swarm behaviors

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into our nanobots as well so we could have extraordinarily large groups of nanobots

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Can we teach them to behave like animals, like insects

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and how do you do this? So the question is interesting.

10:58

So you could think one way to do it would be

11:01

to look at a natural swarm like this one of fish

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and simulate the dynamics of the entire swarm and then try to write the codes

11:09

in molecules of course

11:10

that mimic the same behaviour

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this is virtually impossible, it's impractical

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what we do is we take the single fish or a single nanobot in our case

11:20

and you design a very basic set of interaction rules

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and then you take this one, this nanobot, you make a billion copies of it

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and you let the behaviours emerge from that group

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let me show you some examples of the things we can already do

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for example, just as ants

11:38

can shake hands and form physical bridges between two trees

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or two remote parts of the same tree,

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we already have nanorobots that can reach out for each other

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touch each other and shake hands in such a way

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they form physical bridges.

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Then you can imagine these robots

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extending, making bridges extending from one-half

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to the other half of an injured tissue,

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an injured spinal cord for example

12:00

or an injured leg in the case of Dana, my daughter

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and once they stretched over that tissue gap

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they can apply growth factors, as payloads, and those growth factors

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stimulate the re-growth and guide re-growth of cells across the gap.

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So we already did that and...

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we have robots that can cross regulate each other just like animals do in groups

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and this is amazing because as you can see here

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you can have two types of robots, Type-A and Type-B

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they can cross regulate each other, such that "A" is active

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while "B" is not and viceversa.

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So this is good for combination therapy

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with combination therapy we take multiple drugs, right?

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and sometimes two or more of these drugs

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can collide and generate side effects,

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but here you can put one drug here, one drug here

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and the robots will time the activities so that

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one drug is active, the other is not and then they can switch

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and so two or more drugs can operate at the same time without actually colliding.

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Another example that we did is the quorum sensing.

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Now quorum sensing is great, it's a bacterial inspired behaviour

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It means nanorobots can count themselves

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and they can switch to "on" only when reaching a certain population size

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this is a mechanism invented by bacteria in evolution

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and they regulate amazing behaviours based on just their population density

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for example, bioluminescence, this one of the well-studied examples

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so our robots can count themselves and switch to on

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only when reaching a certain population size which we can program.

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This is great because this is a mechanism of programming a drug

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to become active only when reaching a certain dose

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around the target, regardless of its inherent dose-response curve.

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One last I'm gonna show to you is computing,

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so this nanobots can do computing.

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How's so? If you think about your computer at home,

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the processor of the computer is in fact a gigantic swarm of transistors

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In an i7 core for example you have 800 million transistors approximately

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and they're set to interact in certain ways to produce logic gates

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and these logic gates are set to interact to produce computations

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so we can also produce computation by setting interactions between nanorobots

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to emulate logic gates like you see here

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and they form chains and they form pairs

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and my team in Bar-Ilan University [has] already developed several architectures

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of computing based on interacting nanorobots

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and to prototype these

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we are using animals, very interesting animals

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these are cockroaches,

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they are very easy to work with, the're very sweet,

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they're actually from South America

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and I'm a Soutamerican myself so I fell kinda related

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[Laughter]

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And hum... so what we do is we inject those robots into the cockroach

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and to do that we of course had to put the cockroaches to sleep

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have you ever tried putting cockroach to sleep?

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We put in the freezer for seven minutes

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in they fall asleep

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and we can inject these nanorobots inside

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and after 20 minutes they start running around, they're happy.

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And those robots

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while they're doing this, the robots read molecules

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from the cockroaches' inputs

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and they write their outputs in the form of drugs

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activated on those cockroaches' cells

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so we can do, we can see that and we already have, as you can see,

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architectures of interecting nanorobots that can emulate logical operators

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and you can use these as modular parts to build any type universal computer you want

15:19

[....]

15:21

that can control multiple drugs simultaneously

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as a result of biocomputing, this is real universal computing in a living animal.

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Now we already have systems that have [the] computing capacity

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of an 8-bit computer like Commodore 64.

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To make sure we don't lose control over the nanobots after they're injected

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my team [has] developed nanorobots that carry antennae

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these antennae are made from metal nano-particles.

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Now, the antennae enable the nanobots

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to respond to externally applied electromagnetic fields

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so these nanorobots, this version of nanobots

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can actually be activated with a press of a button on a joystick

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or for example using a controller

16:01

such as the Xbox or Wii if you ever had the chance of playing with those

16:05

and you can see one of my students in the lab configuring an Xbox app

16:09

to control nanobots.

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For example you can imagine nanorobots being injected

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to Dana, my daughter for example,

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and the doctor can guide those robots

16:19

into the site, into the leg and just activate them with a hand gesture.

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And you can already see an example where we actually took

16:26

cancer cells and loaded robots with cancer drugs

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and activated the drug by a hand gesture.

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and we can actually kill cancer cells just by doing this,

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as you can see here.

16:36

And the interesting thing is that

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because the controller like the Xbox is connected to the internet,

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the controller actually links those nanobots to the network

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so they have an actual IP address

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and they can be accessed from a remote device sitting on the same network,

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for example, my doctor's smartphone

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So, OK?, just like controlling a controller, this can be done.

17:00

The last thing I'm gonna show is, if you look at our body

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you'll see that every cell type, every organ, every tissue

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has their own unique molecular signature

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and this is equivalent to a physical IP address made of molecules

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and if you know these molecules

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you can use those nanobots to browse the Organism Wide Web, as we call it

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and you can program them to look for bits,

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this could be for example signally molecules between cells,

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and either fetch them for diagnostics

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or carry them to different addresses.

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And we already have robots that can hijack

17:33

signals between cells

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and manipulate an entire network of communications between cells

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and this is great for controlling very complex diseases in which many cell types

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communicate and orchestrate to perpetuate a disease.

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So before I finish I'd just like to thank

17:50

my amazing team at Bar-Ilan University

17:52

and all the colleagues that took part in this extraordinary journey,

17:55

starting from the George Chuch's Lab in Harvard

17:57

and ending today in Bar-Ilan University in the new Faculty of Life Sciences,

18:01

and I really hope that

18:03

anywhere between a year and five years from now

18:06

we'll be able to use this in humans

18:08

and finally witness the emergence of nanobot society.

18:11

Thank you very much.


https://www.digitaltrends.com/cool-tech/nanobots-live-cockroach-thought-control/





https://www.digitaltrends.com/cool-tech/nanobots-live-cockroach-thought-control/

https://www.timesofisrael.com/israeli-scientists-use-nanobots-and-thoughts-to-administer-drugs/


Israeli scientists say they have come up with a way for brain power to control when drugs are released into the body, by using tiny robots made out of DNA to deliver the medication internally.

Researchers at the Interdisciplinary Center in Herzliya and Bar-Ilan University in Ramat Gan have built the nanobots to which medication is attached and then are injected into the body. The nanobots have a “gate” that opens or closes — thereby controlling drug release — depending on brain activity.

In order to achieve this, the New Scientist magazine said, the researchers developed a computer algorithm that could tell whether a person’s brain was resting or carrying out some form of mental activity, such as math problems. A fluorescent-tinted drug was then added to the nanobots, which were injected into a cockroach placed inside an electromagnetic coil.

Israeli scientists say they have come up with a way for brain power to control when drugs are released into the body, by using tiny robots made out of DNA to deliver the medication internally.

This coil was then connected to an EEG cap worn by a person asked to perform mental calculations. The computer recognized increased brain activity by the cap wearer, which triggered the “gate” on the nanobots inside the cockroach, releasing the fluorescent drug that was visible as it spread through the insect’s body.

The idea is to use the delivery system for people with mental health issues, which are sometimes triggered before sufferers are aware they need medication.

By monitoring brain activity, the nanobots could deliver the required preventative drugs automatically,

for example before a violent episode of schizophrenia.

https://www.newscientist.com/article/2102463-mind-controlled-nanobots-could-release-drugs-inside-your-brain/


The group has built nanorobots out of DNA, forming shell-like shapes that drugs can be tethered to. The bots also have a gate, which has a lock made from iron oxide nanoparticles. The lock opens when heated using electromagnetic energy, exposing the drug to the environment. Because the drug remains tethered to the DNA parcel, a body’s exposure to the drug can be controlled by closing and opening the gate.

By examining when fluorescence appeared inside different cockroaches, the team confirmed that this worked.

The idea would be to automatically trigger the release of a drug when it is needed. For example, some people don’t always know when they need medication – before a violent episode of schizophrenia, for instance. If an EEG could detect it was coming, it could stimulate the release of a preventative drug.

https://www.youtube.com/watch?v=BxJPceCV51g Nanobots Successfully Used on Living Animal for the First Time - IGN News

0:38

to treat human ailments or weaponized

0:40

hijacked by a snake themed terrorist

0:42

organization and then used to destroy

0:43

Paris but I suppose it's only a matter

0:45

of time


“This syringe has inside it a thousand billion robots.”

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https://donshafi911.blogspot.com/2024/04/the-emergence-of-nanobot-society.html

DNA contamination in Covid vaccines DOES get into human cells, new evidence shows
It also appears that the contamination enters the cell nucleus and integrates with human DNA

Rebekah Barnett
Regulators and fact checkers claim that plasmid DNA contamination in the mRNA Covid vaccines can’t change your genomic DNA, but new evidence suggests that it actually can.

The fact checkers assert that DNA contamination poses no risk to your genomic DNA because your body will naturally destroy any contaminant DNA before it even gets into the cells.

Even if the contaminant DNA could get into cells, there’s no way it can enter the cell nucleus, where genomic integration events occur, they say.

And even if the contaminant DNA could enter the nucleus, which it can’t, it still couldn’t genomically integrate unless specific enzymes are present, they say.

However, results from independent lab testing conducted on ovarian cancer cell lines show that contaminant DNA from Pfizer’s Covid vaccine not only crossed into the cells, but that it survived multiple cell divisions. This is suggestive that the contaminant DNA is able to transfect (enter) the cell nucleus, and that it integrated with the human cell DNA.

TLDR

1. Scientists claim that Pfizer vaccine contaminant DNA has been detected in ovarian cancer cell line DNA, but they do not yet know if it’s chromosomal (heritable) or extra-chromosomal DNA (not heritable)

2. This is an in vitro (in a lab dish) finding, and needs to be replicated in vivo (in a human patient)

3. As the finding is specific to cancer cell lines, it is not generalisable, but scientists say it may give an indication of what cancer patients in remission could experience after mRNA Covid vaccination

4. This finding calls into question fact checker claims that mRNA Covid vaccine DNA contamination can't enter cells, can't enter the nucleus, and cannot integrate with human DNA.
Last year, Boston-based genomics scientist Kevin McKernan made the shocking discovery that the mRNA Covid vaccines are contaminated with excessive levels of plasmid DNA, an artefact of the vaccine production process.

McKernan’s findings were soon confirmed by multiple independent labs around the world for both the Pfizer and Moderna mono- and bi-valent vaccines, including lots approved for children, with one Canadian study led by Dr David Speicher concluding that there are “billions to hundreds of billions of DNA molecules per dose.”

Scientists including McKernan, University of South Carolina cancer genomics scientist Dr Phillip Buckhaults, and Dr Wafik El-Diery, head of the Cancer Centre at Brown University, expressed concerns that fragments of plasmid DNA contamination could cause adverse events, autoimmune problems and cancers in some patients.

But perhaps most significantly, there is also a theoretical risk of the contaminant DNA integrating with patients’ chromosomal DNA and modifying the human genome. This is of particular concern with the Pfizer vaccine, which contains an SV40 enhancer sequence, used in gene therapies “to drive DNA into the nucleus,” explains McKernan.

While regulators have taken a ‘wait and see’ approach, independent scientists, including McKernan, have been more proactive, initiating experiments testing for evidence of genomic integration.

Now, the first results are in.

In an experiment conducted together with German molecular biologist Dr Ulrike Kämmerer, McKernan has detected vaccine contaminant DNA in ovarian cancer cell lines treated with Pfizer’s Covid vaccine.

The scientists found a chimeric combination of human ovarian cell line DNA and spike sequence DNA derived from the contaminating plasmid at at least one, and possibly two sites.

“If anything, this work has put to bed the question regarding if this contaminant DNA gets into the cell, and the chimeric human and contaminant spike DNA sequences imply it has entered the nucleus,” McKernan says.

“The PCR and sequencing data both demonstrate the vaccine is getting into the cell and surviving cell passaging. It is likely bioactive and being partially replicated.”

To reach this finding, Dr Kämmerer first treated ovarian cancer cell lines with mRNA Covid vaccines, using cells treated with AstraZeneca and Janssen vaccines as controls.

The cells were then ‘passaged’, meaning they were left to divide and replicate numerous times. This has the effect of “rinsing away residual vaccine,” explains McKernan.

Immunohistochemistry (IHC) was then performed, a staining process that Dr Kämmerer used to detect levels of spike protein expression produced by the vaccine modified-RNA.

This was to confirm that the lipid nanoparticles (LNPs) carrying mod-RNA and plasmid DNA contamination “did their job and delivered the payload,” says McKernan. Measuring how many cells expressed spike protein also allowed the scientists to determine how much of the vaccine to treat the cells with.


Immunohistochemistry performed with Pfizer top left, AstraZeneca top right as a control. Source: Kevin McKernan’s Substack
Cell lines were then sent in cold storage to McKernan’s Boston lab, where his team used qPCR to screen which samples to sequence the cell line DNA.

“What we found is, [contaminant] DNA that is getting transfected into ovarian cancer cell lines is replicating in the cells,” says McKernan, noting that the ratio of vaccine contaminant DNA to human cell DNA was “higher than we expected.”

Chimeric sequences of human and vaccine contaminant DNA were detected at two sites: chromosomes 9 and 12, with the evidence for the latter being the strongest. “But we don't know if it's extra-chromosomal or whether it's chromosomal because of the Illumina (short read) method we used to sequence,” explains McKernan.


Source: Kevin McKernan’s Substack
Extra-chromosomal DNA is not part of the chromosome, and is therefore less likely to replicate and to be heritable. Chromosomal DNA, on the other hand, is heritable and more likely to be replicated. A third category, mitochondrial DNA, is heritable, but only from the maternal line.

You can read a detailed account of methods and findings via McKernan’s Substack article, ‘Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2.’

‘Major advance,’ but clinical implications are limited

McKernan emphasises that these findings cannot be generalised, stating that “it is too early to make comments on the clinical implications.”

“The study is performed in ovarian cancer cell lines. It is not performed in patient cells, but this is a proxy for what might happen in an ovarian cancer patient who's in remission,” says McKernan, especially as there is evidence that the LNPs go to the ovaries.

The risk for patients in this scenario is that integration events with contaminant DNA might cause aberrant cell growth, which poses a risk to immune suppression of new cancer cells.

McKernan notes that his experiment only picked up on putative integration events that persisted after multiple cell replications. That is to say, the scientists were not able to detect integration events that may have occurred, but then died off immediately.

At the moment, no one knows how many integration events might be occurring, or what effect that would have on patients. “The unknowns are just exponential,” says McKernan.

The cancer cell line experiment can be said to be “a microcosm of genome integration of contaminated DNA,” said Japanese molecular oncology scientist Hiroshi Arakawa, in his own analysis of McKernan and Dr Kämmerer’s experiment, published to his popular science blog on which he shares critical views on Covid vaccine safety.

Akira calls the two possible integrations observed in Dr Kämmerer’s experiment a “major advance” laying the ground for further experimentation. “What happens in cultured cells can also occur in normal cells, and a wide variety of abnormalities can occur depending on the site of genome integration,” such as “the induction of cancer or malignant transformation,” he wrote (translated from Japanese to English).

LNPs deliver contaminant DNA straight to the cells

A key assumption underlying claims that mRNA Covid vaccine contamination cannot enter the cell nucleus, and cannot genomically integrate with host DNA, is that the contamination will never make it into dividing cells, which would be required for integration to occur.

This is based on the assumption that the LNPs containing both mod-RNA and contaminant DNA mostly stay in the muscle at the injection site. As muscle cells do not divide, there’s no problem, the logic goes.

This is misleading, however, as Pfizer’s own biodistribution data shows that the LNPs enter the blood and every major organ system, including the ovaries, as mentioned above. While it is true that muscle cells don’t divide, LNPs distributed around the body can transfect any number of dividing cells in various organ systems.


Table 4-2. shows biodistribution of LNPs, Pfizer Nonclinical Evaluation Report, 2021
From there, it’s only a matter of time before the LNP contents get into the cell nucleus, says McKernan. “In any dividing cell, the nucleus dissolves. So, when people say the DNA can get into the cytoplasm [inside the cell membrane] but won't get into the nucleus, well, in any dividing cell, it will end up getting into the nucleus.”

It is possible that the dissolution of the cell nucleus during division is the mechanism underlying McKernan and Dr Kämmerer’s observed passaging of contaminant DNA, but further research will be required to confirm or disprove this hypothesis.

Because of the effectiveness of LNPs in delivering their contents into cells, McKernan, Dr Buckhaults and Dr Speicher have questioned the suitability of the current regulatory limits on contaminant DNA in vaccines, which were set prior to the introduction of LNP technology in vaccines.

Regulators unconcerned

I sent McKernan’s Substack article documenting the new DNA integration findings to Australia’s drug regulator, the Therapeutic Goods Administration, for comment.

The TGA did not address the new findings, but a spokesperson from the TGA responded,

“The Department of Health and Aged Care has every confidence in the safety, quality and efficacy of the various approved COVID-19 vaccines for use in Australia. The TGA’s assessment of all vaccines is based upon high quality evidence, including studies and reviews published in peer-reviewed scientific and clinical journals.”

However, when asked previously to provide evidence for its position that Covid vaccines pose no risk of DNA integration, the TGA provided no peer-reviewed scientific evidence to support its claims.

Instead, the TGA provided links to a Mayo Clinic fact page with no scientific citations, an article by the discredited RMIT FactLab, and a scientific commentary article suggesting that in vitro findings cannot be generalised.

Furthermore, TGA has not been forthcoming with the evidence it does hold. When asked to release Covid vaccine batch testing results under Freedom of Information, the regulator provided all 74 pages - fully redacted.

In the US, the Food and Drug Administration (FDA) denied that contaminant DNA in the mRNA vaccines can enter the nucleus or pose any threat to patients’ genomic DNA, in a response to concerns raised by Florida Surgeon General, Dr Joseph A. Ladapo in December of last year.

Additionally, the FDA misleadingly refuted the presence of SV40 proteins in the vaccines, when in fact Dr Ladapo raised concerns over the presence of an SV40 enchancer sequence in the Pfizer vaccine, as confirmed by Health Canada and numerous independent laboratories.

Such ham-fisted mischaracterisation of a gene therapy sequence by the FDA is suggestive of either gross incompetence, or a disinformation play. Both are concerning.

Science journalist Maryanne Demasi reported, in November last year, that the FDA shut down her enquiries into the DNA contamination matter, refusing to confirm if it found levels of DNA that exceeded acceptable levels, or if it was investigating further.

The presence of contamination has been officially acknowledged by the European Medicines Agency (EMA) and Health Canada, with the latter also acknowledging the presence of the SV40 enhancer sequence, though both regulators deny that the amounts exceed regulatory limits, or that the DNA contamination poses any risk.

‘No excuse’ for ignoring ‘screaming hot signal’

Instead of denying excessive DNA levels and deferring to manufacturers’ reported test results, regulators should run their own qPCR testing on batch lots, says McKernan.

Then, “they would see what everyone else is seeing, which is that sometimes the CT scores come out as low as 13… that’s a screaming hot signal.”

“As a reference, the Covid test would call people positive at 33-35,” McKernan explains. “That’s a million-fold difference (20 CTs). A million-fold less Covid RNA and you're positive and quarantined. But you can inject a million-fold more past your mucosa?”

There’s “no excuse” for regulators to not sequence every vaccine lot, says McKernan, when the costs for doing so have dropped dramatically in recent years.

“DNA sequencing costs have dropped 100,000 fold in the last decade. They have relaxed the DNA contamination limits 1000-fold in this time frame. It likely only costs $1,000 in reagents for millions-to-billions of dollars worth of product.”


Source: National Human Genome Research Institute
DNA sequencing by regulatory agencies is important not just for measuring quantities, says McKernan, but also for determining the type of DNA contamination.

“Not all DNA is created equal. Some is designed to replicate - when it gets into a cell, it can make more of itself. It's a massive loophole in the regulations that they don't do sequencing. But it's never been cheaper. You can precisely know the nature of the DNA in every single vial.”

Scientists pick up regulators’ slack

In the absence of any regulatory appetite for investigating the risks of DNA contamination in the mRNA Covid shots, and particularly the risk of genomic integration, independent scientists have taken the baton.

“We are writing up our findings and will publish a preprint soon,” says McKernan, who is planning further testing in partnership with Dr Kämmerer. “We’re doing more experiments first. We need to sequence deeper to find out if the integration events are in chromosomal or extra-chromosomal DNA.”

Dr Buckhaults is also running his own experiment, calling for de-identified samples of tumours or fresh blood from pathology and hematology labs. These samples will be tested for the presence of plasmid DNA contamination, with whole genome sequencing to then be carried out on positive samples to identify genomic integration sites.

In an email outlining his experiment, Dr Buckhaults told me that he intends to report his findings in a peer-reviewed publication, predicting that the work could take “a few months to a year,” depending on how fast samples come in.

“I am hopeful to prove my concerns are unwarranted by accumulating a lot of negative data, and of course negative data takes the most time to collect,” he said.

McKernan says he is aware of other labs running tests for contaminant plasmid DNA integration, but cannot disclose the details at present.

Decentralisation the future of science?

McKernan says he has experienced some pushback for publishing his methods and findings in real time via Substack, X, and preprints. But, he believes that making his data available as quickly as possible is a way for the field of science to regain public trust.

“Many will criticize our disclosure of preliminary findings but we feel this is an insult to the intelligence of the average person,” says McKernan.

“It's a form of scientific elitism that implies people can't handle the truth and will be scared like sheep if given a glimpse of how the true scientific process is performed. Scientists are 90% of the time wrong but only publish the times when they are right. There is no journal of negative results.“

In light of the prospect that most published research findings are false (as famously asserted in a 2005 article by Professor John Ioannidis), McKernan questions the value of peer-review, instead favouring replication or refutation in the real world.


Source: X
For this reason, McKernan says he has not prioritised peer-reviewed publication for his DNA contamination findings, but is rather focusing on conducting more experiments and releasing the data as he goes - even when it’s incomplete, or requires further experimentation.

“We were not expecting to find any integration events at this depth of coverage, but they are evident to anyone who downloads our public reads. To not speak to obvious evidence in such data would be irresponsible even when such evidence doesn't 100% answer a given question,” says McKernan.

Dr Buckhaults takes a somewhat different view. After sharing his initial plasmid DNA contamination findings in a South Carolina Senate hearing in September last year, the video recording broke the internet.

Believing the hearing to have been private, Dr Buckhaults was alarmed that the widespread distribution of his testimony may have caused “unintended, harmful side effects.” He requested that YouTube take down his testimony video, which is now defunct.


Source: X
In our correspondence, Dr Buckhaults stressed that while more research is warranted, he is of the opinion that the public “should not overreact to the news of the plasmid DNA contamination. It's serious enough that scientists need to hustle and figure out if it's causing any health problems now or down the road, but it's not cause for the general public to be alarmed.”

But, “The reality is that`transfection experiments with contaminated DNA' have been carried out on vast numbers of people around the world in the name of vaccination,” writes Arakawa.

Perhaps the experiment participants will be the ones to decide if they should be alarmed, or not.

The FDA was contacted for comment about Dr Kämmerer and McKernan’s new findings, but they did not respond by publication deadline. This article will be updated if comment is received.

View Kevin McKernan’s write up of his DNA integration experiment (in partnership with Dr Kämmerer) here. Scroll down for links to sequencing data files.

Pathology and hematology labs wishing to send samples to Dr Buckhaults are invited to contact him at the University of South Carolina.

Update 23 March 2024: This article was edited to add mention of the Dr David Speicher et al. finding of “billions to hundreds of billions of DNA molecules per dose” of the mRNA vaccines, and the scientists’ concerns that regulatory limits on DNA contamination have not taken LNP transfection into account.


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From an article I wrote for Umbrella News on this topic last year:

The TGA maintains that allegations put forward in the case about the potential for mRNA vaccines to alter the recipient’s DNA are unfounded. A spokesperson for the TGA told Umbrella News,

“COVID-19 vaccines do not alter a person’s DNA. The mRNA in the vaccines does not enter the nucleus of cells and is not integrated into the human genome. Thus, the mRNA does not cause genetic damage or affect the offspring of vaccinated individuals.”

“The TGA continues to monitor the scientific literature associated with the SARS – CoV-2 virus and the various COVID-19 vaccines approved for use in Australia.”

With reference to the specific studies cited in the case materials, the TGA pointed Umbrella News to an RMIT ABC Fact Check post from 2022 purporting to ‘debunk’ claims that mRNA jabs are genotoxic. This is the same site that ‘debunked’ claims that COVID vaccines can cause menstrual disruption, before peer-reviewed scientific studies proved that they can and do (the post has not been corrected).

As evidence that it is “well established” that vaccine mRNA and protein do not enter the nucleus, the TGA provided a link to a Mayo Clinic fact page which provides no studies or scientific evidence in support of its claims.

The TGA did provide one commentary article published in a scientific journal which pointed out that the in vitro liver cell line study cannot be extrapolated to generalise about in vivo findings (in a human, not a dish) without further research being undertaken.

Additionally, RMIT FactLab was suspended by Facebook in August 2023 after an uproar over its blatantly biased and factually dubious ‘fact checking’ of media articles relating to the Voice referendum campaign. It also transpired that RMIT FactLab had falsely represented its accreditation with the International Fact-Checking Network as current, when it had in fact lapsed.


https://news.rebekahbarnett.com.au/p/dna-contamination-in-covid-vaccines

CDC’s Own Scientists Found Masks Ineffective for Covid-19 but Recommended Them Anyway
Officials at the Centers for Disease Control and Prevention openly questioned the findings of its own scientists’ studies contradicting the agency’s public messaging about mask effectiveness

World Council for Health
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website.

cdc masks ineffective covid feature
The Centers for Disease Control and Prevention’s (CDC) own scientists conducted studies showing N95 respirators are no more effective at stopping viruses than surgical masks — yet the agency issued guidance contradicting those and other studies showing both types of masks are ineffective at stopping the spread of COVID-19, according to an investigation by independent journalist Paul D. Thacker.

The investigation, published this week in two parts on The Disinformation Chronicle, details how CDC leadership openly questioned the findings of CDC scientists’ studies contradicting the agency’s public messaging about mask effectiveness.

During the pandemic, mask advocates “shifted goalposts and demanded N95 respirators,” Thacker said, claiming they perform better than surgical masks at stopping the virus.

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However, Thacker said CDC scientists found no difference between N95 and surgical masks in the ability to stop the spread of respiratory viruses. The findings of the CDC studies are consistent with other peer-reviewed studies on the efficacy of masks in preventing COVID-19, according to Thacker.

“But the CDC responded by saying people can’t say that,” Thacker told The Defender.

To shut down the controversy, the CDC, in its Jan. 23 post on preventing the transmission of pathogens in healthcare settings, warned researchers that to suggest facemasks and respirators are the same “is not scientifically correct,” Thacker wrote.

CDC ignores own studies questioning N95, mask effectiveness

According to Thacker, CDC guidance for controlling the spread of infections had not been updated since 2007. This prompted the CDC, in 2022, to select “a bunch of science experts,” and ask them “to update the agency’s scientific guidance to hospitals on how to control infections.”

In November 2023, the experts produced an 80-page systematic review and meta-analysis, examining whether N95 respirators were more effective than surgical masks. The review found that while N95 respirators are better at filtering particles, the finding that they are more effective at stopping viruses “has been less conclusive.”

The systematic review also examined the “effectiveness” of N95 respirators and surgical masks “under ‘real world’” conditions and found “no difference” between the two.

The review also found numerous symptoms reported by N95 mask users, including: “difficulty breathing, headaches, and dizziness; skin barrier damage and itching; fatigue; and difficulty talking.”

According to Thacker, the CDC is not pleased with these findings, suggesting in its recent update that its own scientists were wrong.

“Although masks can provide some level of filtration, the level of filtration is not comparable to NIOSH Approved respirators,” the CDC said.

The post also stated, “The COVID-19 pandemic has forever changed the approach we take in healthcare settings to protect healthcare personnel, patients, and others from transmission of respiratory infections.”

More evidence contradicting the CDC’s public position came at a June 2023 CDC meeting in Atlanta, when Erin Stone, MPH, a public health analyst in the agency’s Office of Guidelines and Evidence Review, presented the findings of a meta-analysis on the effectiveness of N95 respirators and surgical masks.

According to Stone, the data “suggests no difference” in their effectiveness.

Yet, in November 2023 testimony before the U.S. House of Representatives’ Energy and Commerce Committee, CDC Director Mandy Cohen sidestepped questions regarding mask effectiveness and refused to deny she would reinstate mask mandates for children.

According to Thacker, in December 2023, just six days after Cohen’s testimony, The BMJ’s Archives of Disease in Childhood journal published a study finding that “mask recommendations for children are not supported by scientific evidence.”

“Recommending child masking does not meet the accepted practice of promulgating only medical interventions where benefits clearly outweigh harms,” the study authors noted.

Thacker: CDC guidance based on politics, not science

Thacker said the CDC contradicted its own findings on mask efficacy even in the early stages of the COVID-19 pandemic.

“Soon after the pandemic started, the CDC began promoting masks to stop the spread of COVID,” Thacker wrote. “And it did so despite CDC publishing a May 2020 policy study in their own journal, ‘Emerging Infectious Diseases,’ that did not find a ‘substantial effect’ for masks in stopping the transmission of respiratory viruses.”


twitter.com/CDCgov/status/1378462317109731334
That same month, the CDC began publicly promoting N95 respirators as a more effective means of controlling the spread of COVID-19.

However, on its webpage promoting the superiority of N95 respirators, the CDC admitted “there’s not a whole lot of evidence that N95 respirators do in fact work better than masks at stopping viruses,” Thacker wrote.

“Laboratory studies have demonstrated that FFRs [filtering facepiece respirators] provide greater protection against aerosols compared with surgical masks … however, the results of clinical studies have been inconclusive,” the CDC wrote, citing a 2019 study in JAMA comparing N95 respirators to masks.

“Among outpatient health care personnel, N95 respirators vs medical masks as worn by participants in this trial resulted in no significant difference in the incidence of laboratory-confirmed influenza,” the JAMA study noted.


twitter.com/CDCgov/status/1256655451195715585
According to Thacker, the results of these studies confirm the widely accepted pre-COVID-19 scientific consensus on the ineffectiveness of masks of any kind in stopping the spread of viruses. Thacker cited statements the World Health Organization made in 2019 and the CDC’s guidance on virus control.

In a 2020 appearance on CBS’ “60 Minutes,” Dr. Anthony Fauci said that while a mask might “block a droplet” and “make people feel a little better,” it does not provide “the perfect protection that people think it is.”



According to Thacker, “For some reason, a ‘masks work’ political movement began to grow,” despite Fauci’s statements and the findings of these studies.

“I’m not really sure what happened or what we do next,” Thacker wrote. “But something weird took place in America where liberal elites began messaging among themselves ‘masks work.’ They then grew this into a crusade.”

The movement was effective in getting the CDC on board with issuing mask guidance, Thacker said.

Four years after the onset of the pandemic, the CDC now openly cheerleads for masks, despite research the agency published showing that masks don’t really protect people from catching viruses, he said.

“And this is why the experts advising the CDC are getting all this pushback: they didn’t tell the CDC what the CDC wanted to hear,” Thacker wrote.

Harvey Risch, M.D., Ph.D., professor emeritus and senior research scientist in epidemiology (chronic diseases) at the Yale School of Public Health, told The Disinformation Chronicle the CDC “has succumbed to political influences.”

Risch said:

“It made policies for school closures in order to please the teachers’ union. Its charitable organization allows pharma to feed it hundreds of millions of dollars that would be illegal to go directly to the agency, and this gives pharma major influence on CDC policies.”

According to Thacker, the CDC has continued to double down on guidance promoting mask efficacy. A Jan. 23 letter the agency sent to its own advisers appears to encourage them to add more mask guidance to the agency’s new guidelines for the spread of pathogens, based on the conclusion that N95 respirators are effective.

“Too much science is forcing CDC to request a science do over,” Thacker wrote, referring to the CDC’s Jan. 23 post, which states that its new recommendations should not “be misread to suggest equivalency between facemasks and NIOSH Approved respirators, which is not scientifically correct nor the intent of the draft language.”

Thacker said his investigation shows that “in their guidance to the CDC, experts do recommend masks as part of what they call ‘transmission-based guidance’ which the CDC defines as a second tier of infection control.” However, the CDC’s own guidance also finds that masks are effective only for “source control” — preventing an already infected person from infecting others.

“But this isn’t what the CDC wants,” Thacker wrote. “They want the experts to write guidelines that recommend healthy people wear masks, even though research shows masks won’t really stop healthy people from getting sick.”

“The CDC has caught the ‘masks work’ political wave and is now demanding that independent experts conform to their preferred mask dictates,” he added.

In doing so, the CDC is rejecting science it doesn’t like, including several other non-CDC studies that have questioned mask effectiveness.

A study published in Annals of Internal Medicine in November 2022 found no difference between N95 respirators and surgical masks in stopping the spread of COVID-19. These findings were mirrored in a January 2023 Cochrane meta-analysis on mask effectiveness.

According to the Cochrane report, “The use of a N95/P2 respirators compared to medical/surgical masks probably makes little or no difference for the objective and more precise outcome of laboratory‐confirmed influenza infection.”

A May 2023 study published in Ecotoxicology and Environmental Safety suggests N95 respirators may expose wearers to dangerous levels of toxic compounds linked to seizures and cancer.

A September 2023 meta-analysis published in Clinical Research Study examined mask studies published since 2019 in the CDC’s Morbidity and Mortality Weekly Report (MMWR).

According to the findings of the meta-analysis:

“MMWR publications pertaining to masks drew positive conclusions about mask effectiveness >75% of the time despite only 30% testing masks and <15% having statistically significant results. No studies were randomized, yet over half drew causal conclusions.

“The level of evidence generated was low and the conclusions were most often unsupported by the data. Our findings raise concern about the reliability of the journal for informing health policy.”

Real-world examples also call into question narratives regarding mask efficacy.

Sweden, for instance, did not mandate or recommend masks for the general public during the first wave of the COVID-19 pandemic, and only did so in certain situations in the later stages of the pandemic, according to The Conversation. Yet, its total excess deaths during the first two years of the pandemic were among the lowest in Europe.”

In 2020, Swedish state epidemiologist Anders Tegnell said, “We see no point in wearing a face mask in Sweden, not even on public transport,” adding there were “at least three heavyweight reports … which all state that the scientific evidence is weak.”

A Swedish government commission noted low levels of excess mortality in 2020 and 2021 and said that, at most, masks should have been “recommended.”

Soon after the report was released, a Feb. 25, 2022, Boston Herald op-ed stated that Sweden “got it right.”

“I don’t understand what is driving the ‘masks work’ political movement,” Thacker told The Defender. “There were plenty of stories written pointing out that there isn’t much scientific evidence that masks stop respiratory virus spread.”

“Maybe people were just scared and wanted to believe masks provide protection?” he said.

Thacker also cited the historical precedent of the Spanish Flu epidemic in 1918, when the Red Cross campaigned for masks all across America.

“California’s state board of health ran a study comparing towns that had mask mandates against those that did not. They found that there was no difference and published the study in the American Journal of Public Health in 1920,” Thacker said.

“Maybe these mask campaigners need to read a little history,” he added.

Thacker is now calling on whistleblowers inside the CDC to contact him “to discuss what is going on inside the agency.”

“I’m talking to CDC people and hope to learn what is going on inside the agency. I plan to write more on this,” Thacker told The Defender.

“CDC Director Mandy Cohen wants to restore trust in the agency, but that won’t happen if she keeps putting politics ahead of scientific evidence,” he said.

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This article was written by Michael Nevradakis, Ph.D. and originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.


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https://worldcouncilforhealth.substack.com/p/cdcs-own-scientists-found-masks-ineffective

https://donshafi911.blogspot.com/2024/02/cdcs-own-scientists-found-masks_16.html

CDC'S own scientists conducted studies showing N95 respirators are no more effective at stopping viruses than surgical masks — yet the agency issued guidance contradicting those and other studies showing both types of masks are ineffective at stopping the spread of COVID-19, according to an investigation by Paul D. Thacker.


CDC’s Own Scientists Found Masks Ineffective for COVID — But Agency Recommended Them Anyway
According to an investigation by independent journalist Paul D. Thacker published this week in The Disinformation Chronicle, officials at the Centers for Disease Control and Prevention openly questioned the findings of its own scientists’ studies contradicting the agency’s public messaging about mask effectiveness

Michael Nevradakis, Ph.D.
cdc masks ineffective covid feature
Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free.

The Centers for Disease Control and Prevention’s (CDC) own scientists conducted studies showing N95 respirators are no more effective at stopping viruses than surgical masks — yet the agency issued guidance contradicting those and other studies showing both types of masks are ineffective at stopping the spread of COVID-19, according to an investigation by independent journalist Paul D. Thacker.

The investigation, published this week in two parts on The Disinformation Chronicle, details how CDC leadership openly questioned the findings of CDC scientists’ studies contradicting the agency’s public messaging about mask effectiveness.

During the pandemic, mask advocates “shifted goalposts and demanded N95 respirators,” Thacker said, claiming they perform better than surgical masks at stopping the virus.

However, Thacker said CDC scientists found no difference between N95 and surgical masks in the ability to stop the spread of respiratory viruses. The findings of the CDC studies are consistent with other peer-reviewed studies on the efficacy of masks in preventing COVID-19, according to Thacker.

“But the CDC responded by saying people can’t say that,” Thacker told The Defender.

To shut down the controversy, the CDC, in its Jan. 23 post on preventing the transmission of pathogens in healthcare settings, warned researchers that to suggest facemasks and respirators are the same “is not scientifically correct,” Thacker wrote.

CDC ignores own studies questioning N95, mask effectiveness

According to Thacker, CDC guidance for controlling the spread of infections had not been updated since 2007. This prompted the CDC, in 2022, to select “a bunch of science experts,” and ask them “to update the agency’s scientific guidance to hospitals on how to control infections.”

In November 2023, the experts produced an 80-page systematic review and meta-analysis, examining whether N95 respirators were more effective than surgical masks. The review found that while N95 respirators are better at filtering particles, the finding that they are more effective at stopping viruses “has been less conclusive.”

The systematic review also examined the “effectiveness” of N95 respirators and surgical masks “under ‘real world’” conditions and found “no difference” between the two.

The review also found numerous symptoms reported by N95 mask users, including: “difficulty breathing, headaches, and dizziness; skin barrier damage and itching; fatigue; and difficulty talking.”

According to Thacker, the CDC is not pleased with these findings, suggesting in its recent update that its own scientists were wrong.

“Although masks can provide some level of filtration, the level of filtration is not comparable to NIOSH Approved respirators,” the CDC said.

The post also stated, “The COVID-19 pandemic has forever changed the approach we take in healthcare settings to protect healthcare personnel, patients, and others from transmission of respiratory infections.”

More evidence contradicting the CDC’s public position came at a June 2023 CDC meeting in Atlanta, when Erin Stone, MPH, a public health analyst in the agency’s Office of Guidelines and Evidence Review, presented the findings of a meta-analysis on the effectiveness of N95 respirators and surgical masks.

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According to Stone, the data “suggests no difference” in their effectiveness.

Yet, in November 2023 testimony before the U.S. House of Representatives’ Energy and Commerce Committee, CDC Director Mandy Cohen sidestepped questions regarding mask effectiveness and refused to deny she would reinstate mask mandates for children.

According to Thacker, in December 2023, just six days after Cohen’s testimony, The BMJ’s Archives of Disease in Childhood journal published a study finding that “mask recommendations for children are not supported by scientific evidence.”

“Recommending child masking does not meet the accepted practice of promulgating only medical interventions where benefits clearly outweigh harms,” the study authors noted.

Thacker: CDC guidance based on politics, not science

Thacker said the CDC contradicted its own findings on mask efficacy even in the early stages of the COVID-19 pandemic.

“Soon after the pandemic started, the CDC began promoting masks to stop the spread of COVID,” Thacker wrote. “And it did so despite CDC publishing a May 2020 policy study in their own journal, ‘Emerging Infectious Diseases,’ that did not find a ‘substantial effect’ for masks in stopping the transmission of respiratory viruses.”


That same month, the CDC began publicly promoting N95 respirators as a more effective means of controlling the spread of COVID-19.

However, on its webpage promoting the superiority of N95 respirators, the CDC admitted “there’s not a whole lot of evidence that N95 respirators do in fact work better than masks at stopping viruses,” Thacker wrote.

“Laboratory studies have demonstrated that FFRs [filtering facepiece respirators] provide greater protection against aerosols compared with surgical masks … however, the results of clinical studies have been inconclusive,” the CDC wrote, citing a 2019 study in JAMA comparing N95 respirators to masks.

“Among outpatient health care personnel, N95 respirators vs medical masks as worn by participants in this trial resulted in no significant difference in the incidence of laboratory-confirmed influenza,” the JAMA study noted.


According to Thacker, the results of these studies confirm the widely accepted pre-COVID-19 scientific consensus on the ineffectiveness of masks of any kind in stopping the spread of viruses. Thacker cited statements the World Health Organization made in 2019 and the CDC’s guidance on virus control.

In a 2020 appearance on CBS’ “60 Minutes,” Dr. Anthony Fauci said that while a mask might “block a droplet” and “make people feel a little better,” it does not provide “the perfect protection that people think it is.”



According to Thacker, “For some reason, a ‘masks work’ political movement began to grow,” despite Fauci’s statements and the findings of these studies.

“I’m not really sure what happened or what we do next,” Thacker wrote. “But something weird took place in America where liberal elites began messaging among themselves ‘masks work.’ They then grew this into a crusade.”

The movement was effective in getting the CDC on board with issuing mask guidance, Thacker said.

Four years after the onset of the pandemic, the CDC now openly cheerleads for masks, despite research the agency published showing that masks don’t really protect people from catching viruses, he said.

“And this is why the experts advising the CDC are getting all this pushback: they didn’t tell the CDC what the CDC wanted to hear,” Thacker wrote.

Harvey Risch, M.D., Ph.D., professor emeritus and senior research scientist in epidemiology (chronic diseases) at the Yale School of Public Health, told The Disinformation Chronicle the CDC “has succumbed to political influences.”

Risch said:

“It made policies for school closures in order to please the teachers’ union. Its charitable organization allows pharma to feed it hundreds of millions of dollars that would be illegal to go directly to the agency, and this gives pharma major influence on CDC policies.”

According to Thacker, the CDC has continued to double down on guidance promoting mask efficacy. A Jan. 23 letter the agency sent to its own advisers appears to encourage them to add more mask guidance to the agency’s new guidelines for the spread of pathogens, based on the conclusion that N95 respirators are effective.

“Too much science is forcing CDC to request a science do over,” Thacker wrote, referring to the CDC’s Jan. 23 post, which states that its new recommendations should not “be misread to suggest equivalency between facemasks and NIOSH Approved respirators, which is not scientifically correct nor the intent of the draft language.”

Thacker said his investigation shows that “in their guidance to the CDC, experts do recommend masks as part of what they call ‘transmission-based guidance’ which the CDC defines as a second tier of infection control.” However, the CDC’s own guidance also finds that masks are effective only for “source control” — preventing an already infected person from infecting others.

“But this isn’t what the CDC wants,” Thacker wrote. “They want the experts to write guidelines that recommend healthy people wear masks, even though research shows masks won’t really stop healthy people from getting sick.”

“The CDC has caught the ‘masks work’ political wave and is now demanding that independent experts conform to their preferred mask dictates,” he added.

In doing so, the CDC is rejecting science it doesn’t like, including several other non-CDC studies that have questioned mask effectiveness.

A study published in Annals of Internal Medicine in November 2022 found no difference between N95 respirators and surgical masks in stopping the spread of COVID-19. These findings were mirrored in a January 2023 Cochrane meta-analysis on mask effectiveness.

According to the Cochrane report, “The use of a N95/P2 respirators compared to medical/surgical masks probably makes little or no difference for the objective and more precise outcome of laboratory‐confirmed influenza infection.”

A May 2023 study published in Ecotoxicology and Environmental Safety suggests N95 respirators may expose wearers to dangerous levels of toxic compounds linked to seizures and cancer.

A September 2023 meta-analysis published in Clinical Research Study examined mask studies published since 2019 in the CDC’s Morbidity and Mortality Weekly Report (MMWR).

According to the findings of the meta-analysis:

“MMWR publications pertaining to masks drew positive conclusions about mask effectiveness >75% of the time despite only 30% testing masks and <15% having statistically significant results. No studies were randomized, yet over half drew causal conclusions.

“The level of evidence generated was low and the conclusions were most often unsupported by the data. Our findings raise concern about the reliability of the journal for informing health policy.”

Real-world examples also call into question narratives regarding mask efficacy.

Sweden, for instance, did not mandate or recommend masks for the general public during the first wave of the COVID-19 pandemic, and only did so in certain situations in the later stages of the pandemic, according to The Conversation. Yet, its total excess deaths during the first two years of the pandemic were among the lowest in Europe.”

In 2020, Swedish state epidemiologist Anders Tegnell said, “We see no point in wearing a face mask in Sweden, not even on public transport,” adding there were “at least three heavyweight reports … which all state that the scientific evidence is weak.”

A Swedish government commission noted low levels of excess mortality in 2020 and 2021 and said that, at most, masks should have been “recommended.”

Soon after the report was released, a Feb. 25, 2022, Boston Herald op-ed stated that Sweden “got it right.”

“I don’t understand what is driving the ‘masks work’ political movement,” Thacker told The Defender. “There were plenty of stories written pointing out that there isn’t much scientific evidence that masks stop respiratory virus spread.”

“Maybe people were just scared and wanted to believe masks provide protection?” he said.

Thacker also cited the historical precedent of the Spanish Flu epidemic in 1918, when the Red Cross campaigned for masks all across America.

“California’s state board of health ran a study comparing towns that had mask mandates against those that did not. They found that there was no difference and published the study in the American Journal of Public Health in 1920,” Thacker said.

“Maybe these mask campaigners need to read a little history,” he added.

Thacker is now calling on whistleblowers inside the CDC to contact him “to discuss what is going on inside the agency.”

“I’m talking to CDC people and hope to learn what is going on inside the agency. I plan to write more on this,” Thacker told The Defender.

“CDC Director Mandy Cohen wants to restore trust in the agency, but that won’t happen if she keeps putting politics ahead of scientific evidence,” he said.

DETAILS
https://childrenshealthdefense.org/defender/cdc-scientists-masks-ineffective-covid-agency-recommended/

Join @ShankaraChetty


https://donshafi911.blogspot.com/2024/02/cdcs-own-scientists-found-masks.html

Virology - The Damning Evidence
The Stake In The Heart For This Pseudoscientific Profession

dpl
Introduction

One never realize how big the task of writing on a subject is until you start. One thing you can be assured of is how much you learn by writing about your findings or thoughts. My stance on virology has been clarified in two previous posts as follows:

The Gatekeepers Club.

Virus Lie - The Result of 4 Years of Study.

Another thing you quickly realize on this journey is how easy it is to censor someone, especially if you start hitting a nerve. I have documented some of it underneath the conclusion of the The Gatekeepers Club article. It is very important to make copies of your work, as shadow banning is one thing, but if these platforms decide to terminate your channel and all the work you have done is on it, you will obviously lose it all. We were in that same position about a year ago when Discord decided to terminate our channel. Twenty of the smartest people you would ever know had been working on it for close to two years, and it was gone overnight. Therefore, this post will serve as safekeeping for some of the best information that I have come across in the last few weeks proving that virology is pseudoscience.


Update - 18 September 2023

The order of the sections of this article has been rearranged to introduce the most important information first. As mentioned in my most recent article titled: Hacking at the Root of the Virus Issue it was explained that for the longest time I thought that failure to “isolate” viruses was the most important evidence to focus on. This is however not the case as explained in detail in the “Hacking at the Root of the Virus Issue” article.

Transmission is the fundamental assumption on which virology rest. Without proof of transmission, nothing downstream matters. Even though understanding these downstream concepts will never be a waste of time one must consider that the normal man on the street will not be interested in complicated terminology and processes.

It is of crucial importance for the no virus community to find easier ways to explain the fallacy that is virology. Seeing as no one need a laboratory to assess whether transmission is possible and because we can observe this phenomena ourselves (Inductive reasoning) this is the linchpin for virology. A twitter space where we discussed this can be viewed here (*Note: Jamie was cut off during his talk and his section was not included).

As discussed during the twitter space, we have reviewed the available transmission studies and a summary of these studies can be seen below.

Transmission / Infection

One of the funniest things you will see while debating the trolls on Twitter is that they will provide studies conducted to prove the efficacy of vaccines. The people that undertake these studies assume that transmission or infection has already been proven, but nothing could be further from the truth. That is why it is important for us to list the peer-reviewed studies that disprove transmission or infection to further demonstrate that virology is a pseudoscience. The list of studies was compiled with the help of Jamie, georgie&donny, and Aldhissla (also see Aldhissla’s list on polio here).

(*Please note that this section is open to comments at the moment and anyone that want to add notes or studies are free to leave a comment).

The Journal of Infectious Diseases, Vol. 2, No. 2 (Mar. 1, 1905):
- Chapman, 1801: Tried to transmit measles using the blood, tears, the mucus of the nostrils and bronchia, and the eruptive matter in the cuticle without any success.
- Willan, 1809: Inoculated three children with vesicle fluids of measles but without success.
- Albers, 1834: Attempted to infect four children with measles without success. He quoted Alexander Monro, Bourgois, and Spray as also having made unsuccessful inoculations with saliva, tears, and cutaneous scales.
- Themmen, 1817: Tried to infect 5 children with measles. 0/5 children became sick.

Charles Creighton, 1837 (A history of epidemics in Britain). "No proof of the existence of any contagious principles by which it was propagated from one individual to another."

EH Ackernecht, writing about Anticontagionism between 1821 and 1867 - “That the anticontagionists were usually honest men and in deadly earnest is shown, among other things, by the numerous self-experiments to which they submitted themselves to prove their contentions.” also see “Famous are the plague self-experiments of Clot-Bey, the offers for plague self-experiment by Chervin, Lassis, Costa, Lapis, and Lasserre, and the cholera self-experiments of Fay, Scipio Pinel, Wayrot, and J.L. Guyon. The amazing thing is that almost all of these experiments failed to produce the disease.”

Note on Hospitals by Florence Nightingale, 1858 - "Suffice it to say, that in the ordinary sense of the word, there is no proof, such as would be admitted in any scientific inquiry, that there is any such thing as 'contagion." also see "Just as there is no such thing as 'contagion,' there is no such thing as inevitable 'infection."

Andreas Christian Bull, 1868 - “It does not seem apparent in this small [polio] epidemic that contagion played any role, because the disease occurred here and there in the different places of the district without the possibility of establishing any relation between the various cases or the families of the same.”

Karl-Oskar Medin, 1887 - A Swedish pediatrician who was the first to examine a polio outbreak, concluded that it was an infectious, but not contagious, disease.

Charles Caverly, 1894 - Investigated the first US polio epidemic: ”it is very certain that it was non-contagious.”

Journal of American Medical Association, Volume 72, Number 3, 1919 (or additional link here):

- Warschawsky, 1895 - Injected small pigs and rabbits with blood taken in the eruptive stage. All results were negative.
- Belila, 1896 - Placed warm nasal mucus and saliva from measles patients on the nasal and oral mucous membrane of rabbits, guinea-pigs, cats, mice, dogs and lambs, but without any positive results.
- Josias, 1898 - Rubbed measles secretions over the throat, nose and eyes of several young pigs, but without any effects.
- Geissler, 1903 - Inoculated sheep, swine, goats, dogs and cats in various ways with the bodily fluids from patients with measles; including smearing, spraying, rubbing. All results were negative.
- Pomjalowsky, 1914 - Injected measles blood into guineapigs, rabbits and small pigs. All results were negative.
- Jurgelunas, 1914 - Inoculated blood from patients with measles into suckling pigs and rabbits, but without effect.

Leegaard, 1899 - Was not able to prove a single case of patient-to-patient contagion in a polio outbreak in Norway. "Infantile paralysis is of an infectious, but not of a contagious nature. As a matter of fact no indisputable instance of contagion could be proved."

Dr. Rodermund, 1901 - From his diary of SmallPox experiments. For 15 years he smeared the pus of smallpox patients on his face and used to go home with his family, play cards at the gentleman’s club and treat other patients and never got sick or saw a single other person get sick.

Walter Reed, 1902 - “Without entering into details, I may say that, in the first place, the Commission saw, with some surprise, what had so often been noted in the literature, that patients in all stages of yellow fever could be cared for by non-immune nurses without danger of contracting the disease. The non-contagious character of yellow fever was, therefore, hardly to be questioned.”

Landsteiner & Popper, 1909 - "Attempts to transmit the disease [polio] to the usual laboratory animals, such as rabbits, guinea pigs, or mice, failed."

F.E. Batten, (1909) - “Against the infectivity of the disease may be urged, first, the absence of spread of infection in hospital. The cases of poliomyelitis admitted to hospital freely mixed with other cases in the ward without any isolation or disinfection, some 70 children came in contact, but no infection took place. (p. 208, last paragraph)”

The Boston medical and surgical journal, 1909 - An inquiry a 1908 polio outbreak found the following: “A large number of children were in intimate contact with those that were sick, and of these children an insignificant minority developed the disease.” 244 children were in intimate contact with those who were afflicted with polio. Of those 244 children, an "insignificant minority" developed the disease.

Massachusetts State board of health, 1909 - "Poliomyelitis prevailed in epidemic form in Kansas during the summer of 1909 … No method of contagion could be found, and the author does not consider the disease contagious."

Flexner & Lewis, 1910 - Multiple unsuccessful polio transmission attempts. "Many guinea-pigs and rabbits, one horse, two calves, three goats, three pigs, three sheep, six rats, six mice, six dogs, and four cats have had active virus introduced in the brain but without causing any appreciable effect whatever. These animals have been under observation for many weeks."

A Washinton, 1911 - “I have not seen any cases of Polio contagion. We put the patients on one side and typhoid cases on the other, and no nurse or mother was infected. If the disease was so contagious, I don't see why the nurses and mothers would not have been infected.”

J.J. Moren, 1912 - "Monkeys suffering from polio in the same cage with healthy monkeys, do not infect others."

P. H. Römer, 1913 - "No proofs of the contagiousness of the disease [polio] could be obtained in the great epidemic in New York in 1907, nor in the epidemic in the Steiermark (Furntratt, Potpeschnigg) nor in Pomerania (Peiper).

H. W. Frauenthal, 1914 - "Advocates of the contagion theory were at a loss to account for the fact that spontaneous [polio] transmission among laboratory monkeys was never known to occur ... There is no proof that spontaneous transmission of acute poliomyelitis, without an inoculation wound, can take place. There is no proof that contact contagion takes place. Spontaneous development of the disease among laboratory animals is unknown."

W.H. Frost, 1916 - "The disease [polio] develops in a such a small proportion of people known to have been intimately associated with acute cases of polio." ... "The majority of cases of poliomyelitis can not be traced to known contact, either direct or indirect, with any previous case."

W. L. Holt, 1916 - Investigated an epidemic of polio and found that he was "surprised that I could trace hardly any cases to personal contact with others, there rarely being successive cases."

Dr. I. D. Rawlings, 1916 - "Any one who has had much experience with poliomyelitis is struck by the infrequency, relatively, of the secondary cases among direct contacts ... there were approximately 1,500 direct contacts, and yet but one possible case occurred among them. Also among the large number of people that came from New York and other infected areas not a single case occurred.”

H. L. Abramson, 1917 - Attempts to induce polio in a monkey by injecting the spinal fluid of 40 polio patients (rather than the ground cord) into the brain failed.

Dold et al. 1917 (Original paper in German from Muenchener Medizinische Wochenschrift 64 ( 1917), bottom of p 143) - Injected healthy people with the nasal secretions taken from one ill person, 1/40 healthy people became ill.

A review of the investigations concerning the etiology of measels, A. W. Sellards
harvard Medical School. Boston, Massachusetts as seen below:
- Jurgelunas, 1914: Tried to produce measles in monkeys using inoculations of the blood and mucus secretions from measles patients as well as by exposing the animals to patients in measles wards. All results were negative.
- Sellards, 1918: Tried to transmit measles to 8 healthy volunteers without a prior history of measles exposure. 0/8 men became sick after multiple failed attempts.
- Sellards and Wenworth, 1918: Inoculated 3 monkeys in various ways, including intensive injections of blood from measles patients. The animals remained well.
- Sellards and Wenworth, 1918: Blood from measles patients was injected simultaneously into 2 men and 2 monkeys. Both men remained symptom-free. One of the two monkeys developed symptoms that were not suggestive of measles.

Milton Rosenau, 1918 - Professor of preventive medicine and hygiene at Harvard, notes that "monkeys have so far never been known to contract the disease [polio] spontaneously, even though they are kept in intimate association with infected monkeys." Page 341.

Hess & Unger, 1918 - "In three instances the nasal secretion of varicella patients was applied to the nostrils; in three others the tonsillar secretion to the tonsils, and in six, the tonsillar and pharyngeal secretions were transferred to the nose, the pharynx, and the tonsils. In none of these twelve cases was there any reaction whatsoever, either local or systemic."

Hess & Unger, 1918 - The vesicle fluids from people with chickenpox was injected intravenously into 38 children. 0/38 became sick.

Published in the Journal - American Medical Association, 1919 - Need Of Further Research On The Transmissibility Of Measles And Varicella. “Evidently in our experiments we do not, as we believe, pursue nature's mode of transmission; either we fail to carry over the virus, or the path of infection is quite different from what it is commonly thought to be.”

Milton J. Rosenau, March 1919 - Conducted 9 separate experiments in a group of 49 healthy men, to prove contagion. In all 9 experiments, 0/49 men became sick after being exposed to sick people or the bodily fluids of sick people.

More information on the Rosenau studies here.

Wahl et al, 1919 - Conducted 3 separate trials on six men attempting to infect them with different strains of Influenza. Not a single person got sick.

Schmidt et al, 1920 (Original paper in German here) - Conducted two controlled experiments, exposing healthy people to the bodily fluids of sick people. Of 196 people exposed to the mucous secretions of sick people, 21 (10.7%) developed colds and three developed grippe (1.5%). In the second group, of the 84 healthy people exposed to mucous secretions of sick people, five developed grippe (5.9%) and four colds (4.7%). Of forty-three controls who had been inoculated with sterile physiological salt solutions eight (18.6%) developed colds. A higher percentage of people got sick after being exposed to saline compared to those being exposed to the “virus”.

Williams et al, 1921 - Tried to experimentally infect 45 healthy men with the common cold and influenza, by exposing them to mucous secretions from sick people. 0/45 became ill.

Mahatma Gandhi, 1921 - "and the poison that accumulates in the system is expelled in the form of small-pox. If this view is correct, then there is absolutely no need to be afraid of small-pox" also see "This has given rise to the superstition that it is a contagious disease, and hence to the attempt to mislead the people into the belief that vaccination is an effective means of preventing it."

Blanc and Caminopetros, 1922 (original paper in French here) - Material from nine cases of shingles was inoculated into the eyes, cornea, conjunctiva, skin, brain, and spinal cord of a series of animals, including rabbits, mice, sheep, pigeons, monkeys, and a dog. All results were negative.

Robertson & Groves, 1924 - Exposed 100 healthy individuals to the bodily secretions from 16 different people suffering from influenza. 0 people of 100 whom they deliberately tried to infect with Influenza got sick That is because Viruses don't cause disease.

Bauguess, 1924 - "A careful search of the literature does not reveal a case in which the blood from a patient having measles was injected into the blood stream of another person and produced measles."

The problem of the etiology of herpes zoster, 1925 - "Many other authors report entirely negative results following the inoculation of herpes zoster material into the sacrified corneas of rabbits: Kraupa (18); Baum (19); LSwenstein (8), Teissier, Gastinel, and Reilly (20) ; Kooy (21) ; Netter and Urbain (22); Bloch and Terris (23); Simon and Scott (24); and Doerr (25). It is evident, therefore, that the results of attempts to inoculate animals with material from cases of herpes zoster must be considered at present to be inconclusive."

Volney S and Chney M.D., 1928 - A study where it is clearly stated that cold is not infectious.

Dochez et al, 1930 - Attempted to infect 11 men with intranasal influenza. Not a single person got sick. Most strikingly one person got very sick when he accidently found out that is what they were trying to do. His symptoms disappeared when they told him he was misinformed.

L. L. Lumsden, 1935 - “Painstaking efforts were made throughout the studies to obtain all traces of transmission of the disease through personal contact, but it appears that in this outbreak in Louisville evidence of personal association between the cases of poliomyelitis, suggestive of cause and effect, was no more common than that which might have been found if histories had been taken of personal association between cases of broken bones occurring in the city in the same period.”

Thomas Francis Jr et al, 1936 - Gave 23 people influenza via 3 different methods. 0 people got sick.. They gave 2 people already "suffering from colds" the influenza who also did not get sick

Burnet and Lush, 1937 - 200 people given "Melbourne type" Influenza . 0 people showed any symptoms of disease. 200/0.

Lumsden, 1938 - "It is quite usual in small [polio] outbreaks in rural counties for individual cases to develop in separate homes three or for miles apart without there being any evidence of direct or indirect personal contact having operated between persons afflicted."

L. L Lumsden, 1938 - ”The general and usual epidemiological features of the disease [polio] all appear opposed to the hypothesis that poliomyelitis is a contagious disease spread among human beings by nose-to-nose or any other direct personal contact.”

Burnet and Foley, 1940 - Attempted to experimentally infect 15 university students with influenza. The authors concluded their experiment was a failure.

Thomas Francis Jr, 1940 - Gave 11 people "Epidemic Influenza" 0 people got sick. That is because viruses don't cause disease.

John Toomey, 1941 - A veteran polio researcher: "no animal gets the disease from another, no matter how intimately exposed."

A. R. Kendall, 1945 - “The epidemiological facts of poliomyelitis are these: … (2) A majority of cases of clinically diagnosable poliomyelitis (polioparalysis) occur sporadically, with no history of contact with previous cases. (3) Two cases of polioparalysis in one family are unusual, even though no precautions are taken to prevent cross infection. (4) Clinically diagnosable cases of poliomyelitis (polioparalysis) show little tendency to spread, even in schools or other places of public gathering. (5) Incidence of polioparalysis is no greater among doctors and nurses, in intimate contact with acute cases than it is among the civil population, even though the former are exposed freely to infection.” […] “Polioparalysis is not contagious.”

E. B. Shaw & H. E. Thelander, 1949 - “The epidemiology of the disease [polio] remains obscure. There has been a tendency to depart from an early theory that the disease spreads by means of direct contact.”

Albert Sabin, 1951 (inventor of the polio vaccine). "There is no evidence for the transmission of poliomyelitis by droplet nuclei."

Archibald L. Hoyne, 1951 (alternative link here) - “However, in the Cook County Contagious Disease Hospital where the latter procedure has not been used there has never been a doctor, intern, nurse or any other member of the personnel who contracted poliomyelitis within a period of at least thirty-five years, nor has any patient ever developed poliomyelitis after admission to the hospital.”

Ralph R. Scobey, 1951 - ”Although poliomyelitis is legally a contagious disease, which implies that it is caused by a germ or virus, every attempt has failed conclusively to prove this mandatory requirement of the public health law.” Professor of clinical pediatrics and president of the Poliomyelitis Research Institute, Syracuse, N.Y.

Ralph R. Scobey, 1952 - "In addition to the failure to prove contagiousness of human poliomyelitis, it has likewise been impossible to prove contagiousness of poliomyelitis in experimental animals."

Douglas Gordon et al, 1975 - This study gave 10 people English type Influenza and 10 people a placebo. The study was negative. Most telling is they admit that mild symptoms were seen in the placebo group, proving that the inoculation methods cause them.

Beare et al 1980 (refer to reference 6 in the linked paper). Quote from John J Cannell, 2008 as follows - “An eighth conundrum – one not addressed by Hope-Simpson – is the surprising percentage of seronegative volunteers who either escape infection or develop only minor illness after being experimentally inoculated with a novel influenza virus.”

Nancy Padian, 1996 - A study which followed 176 discordant couples (1 HIV positive and the other negative) for 10 years. These couples regularly slept together and had unprotected sex. There were no HIV transmissions from the positive partner to the negative partner during the entirety of the study.

John Treanor et al, 1999 - Gave 108 people Influenza A. Only 35% recorded mild symptoms such as stuffy nose. Unfortunately 35% of the placebo control group also developed mild symptoms proving the methods of inoculation are causing them.

Bridges et al, 2003 - "Our review found no human experimental studies published in the English-language literature delineating person-to-person transmission of influenza... Thus, most information on human-to-human transmission of influenza comes from studies of human inoculation with influenza virus and observational studies."

The Virology Journal, 2008 - ”There were five attempts to demonstrate sick-to-well influenza transmission in the desperate days following the pandemic [1918 flu] and all were ’singularly fruitless’ … all five studies failed to support sick-to-well transmission, in spite of having numerous acutely ill influenza patients, in various stages of their illness, carefully cough, spit, and breathe on a combined total of >150 well patients.”

Public Health Reports, 2010 - ”It seemed that what was acknowledged to be one of the most contagious of communicable diseases [1918 flu] could not be transferred under experimental conditions.”

Jasmin S Kutter, 2018, - Our observations underscore the urgent need for new knowledge on respiratory virus transmission routes and the implementation of this knowledge in infection control guidelines to advance intervention strategies for currently circulating and newly emerging viruses and to improve public health.
- There is a substantial lack of (experimental) evidence on the transmission routes of PIV (types 1–4) and HMPV.
- Extensive human rhinovirus transmission experiments have not led to a widely accepted view on the transmission route [35, 36, 37, 38, 39, 40].
- However, until today, results on the relative importance of droplet and aerosol transmission of influenza viruses stay inconclusive and hence, there are many reviews intensively discussing this issue [10, 45, 46, 47, 48, 49, 50].
- Despite this, the relative importance of transmission routes of respiratory viruses is still unclear, depending on the heterogeneity of many factors like the environment (e.g. temperature and humidity), pathogen and host [5, 19].

Jonathan Van Tam, 2020 - Conducted these human trials of Flu A in 2013. 52 people were intentionally given "Flu A" and made to live in controlled conditions with 75 people. 0 people sick. 0 PCR positive.

J.S. Kutter, 2021 - “Besides nasal discharge, no other signs of illness were observed in the A/H1N1 virus-positive donor and indirect recipient animals.” The animals were subsequently euthanized after the animals experienced what the scientist describe as having breathing difficulties (no further details were given to describe their condition). *Refer to Note 1.

Ben Killingley, 2022 - Gave 36 people what he considered to be purified Covid Virus Intranasally. The Results: Nobody got sick. *Refer to Note 2.

Notes

*Note 1 - Jasmin Kutter, 2021:

From the Results section: “Throat and nasal swabs were collected from the donor and indirect recipient animals on alternating days.” This on its own can lead to nasal discharge which is the only “sign of illness” that was noted in this study.

*Note 2 - Ben Killingley, 2022:

See the video explanation by Jamie here.

Ben Killingley also conducted a study in the early 2010's in which he had inoculated people in a room with 75 others some wearing masks others as a control. Not a single person even tested PCR positive. Some links to his previous studies include a 2011, 2019 and a 2020 study.

It is assumed that his latest, 2022 study, is a follow up to cover the findings of his previous findings. Some additional notes on the study referenced include:

- They gave 10 people the potent nephrotoxin Remdisivir.

- They measure sickness by means of a PCR test which isn't indicative of disease because it can tests positive with “asymptomatic” cases as well.

- Even if you say that a runny nose after swabbing is Covid. A 50% outcome to a direct challenge of something is a negative result. It doesn't suggest causation which would need to be at least 90%.

- The very methods of inoculation used during the study could cause the nasal congestion/discharge (which is their measure of whether someone is sick or not). This has been shown in previous studies.

- Lastly nobody was given "regeneron" because nobody got "sick".

*Note 3 - Dr Robert Willner, 1994:

December 7th 1994 Hollywood Roosevelt Hotel, Greensboro, N.C., Dr Willner (a medical doctor of 40 years experience) an outspoken whistleblower of the AIDS hoax. In front of a gathering of about 30 alternative-medicine practitioners and several journalists, Willner stuck a needle in the finger of Andres, 27, a Fort Lauderdale student who says he has tested positive for HIV. Then, wincing, the 65-year-old doctor stuck himself. In 1993, Dr. Willner stunned Spain by inoculating himself with the blood of Pedro Tocino, an HIV positive hemophiliac. This demonstration of devotion to the truth and the Hippocratic Oath he took, nearly 40 years before, was reported on the front page of every major newspaper in Spain. His appearance on Spain’s most popular television show envoked a 4 to 1 response by the viewing audience in favor of his position against the “AIDS hypothesis.” When asked why he would put his life on the line to make a point, Dr. Willner replied: “I do this to put a stop to the greatest murderous fraud in medical history. By injecting myself with HIV positive blood, I am proving the point as Dr. Walter Reed did to prove the truth about yellow fever. In this way it is my hope to expose the truth about HIV in the interest of all mankind.” He tested negative multiple times. He died of a Heart attack 4 months later 15th April 1995 (yeh right, funny how these naysayers all die suddenly. Link to the presentation here.

Ludicrous “Transmission” Studies

The picture of virology’s ludicrousy won’t be complete without a list of studies showing the insanity of what virologists claim to be transmission of disease. This include the injection of fluids into the brains and lungs of animals and we may just include some epidemiological studies to show how these are also not proof of anything. Joe Hendry mostly put it together and the papers we have are as follows (*Please note that this section is open to comments at the moment and anyone that want to add notes or studies are free to leave a comment):

Louis Pasteur, 1881 - For rabies, tried to demonstrate transmission by injecting diseased brain tissue "directly onto the surface of the brain of a healthy dog through a hole drilled into its skull."

Simon Flexner and Paul A. Lewis, 1910 - Spinal cords from deceased children were ground up and emulsified to be injected into the brains of monkeys. Study explained in detail here.

John F. Anderson and Joseph Goldberger, 1911 - Injected blood from a measles patient directly into the heart and brains of monkeys.

Carl Tenbroeck, 1918 - A mixture of ground up rat's livers, spleens, kidneys,
testicles, lungs, hearts, and brains was injected into the brains of other rats.

Claus W. Jungeblut, 1931 - Ground up monkey spinal cord was injected into the brains of other monkeys.

Wilson Smith, 1933 - “The infected animal is killed when showing symptoms, often at the beginning of the second temperature rise. The turbinates are scraped out, ground up with sand, and emulsified in about 20 c.cm. of equal parts of broth and saline. The emulsion is lightly centrifuged, and about 1 c.cm. of the supernatant fluid is dropped into the nostrils of another ferret.”

Thomas Francis and Jr, T. P. Magill, 1935 - Ground up ferret lung tissue was injected into the brains of rabbits.

Ann G. Kuttner and T'sun T'ung, 1935 - Ground up kidney and brain of a guinea pig was injected into the brain of another guinea pig.

Erich Traub. April 01 1936 - Ground up mouse brain was injected into the brains of guinea pigs.

Albert B. Sabin and Peter K. Olitsky, 1937 - Ground up mouse brain was injected into the brains of other mice.

G. John Buddingh, 1938 - Ground up chick embryo was injected into the brains 2 or 3 day old chicks.

Gilbert Dalldorf, 1939 - Ground up ferret spleens was injected into the brains of mice.

Claus W. Jungeblut et al, 1942 - Ground up brain or spinal cord of paralyzed mice was injected into the brains of 13 monkeys.

Henry Pinkerton and Vicente Moragues, 1942 - Ground up brain tissue from dying mice was injected into the brains of pigeons.

C. Kling et al, 1942 - Injected sewage sludge into the brains and abdomen of monkeys. This convinced him that he had isolated a virus and proven that the sewer is a vehicle for polio transmission.

D.M. Horstmann, 1944 - Allegedly "proved" that the feces of polio patients contained "poliovirus" by injecting fecal samples into monkeys' brains and spines.

Joseph E. Smadel et al, 1945 - Ground up pigeon spleen was injected into the brains of mice.

F. Sargent Cheever et al, 1949 - Ground up mouse brain was injected into the brains of rats and hamsters.

Isolation

Isolation has been well defined in Virus Lie - The Result of 4 Years of Study and to this day there has not been a single paper presented that could show the isolation of a virus without first contaminating the sample. This is shown in detail in the virus lie article and will not be repeated here again. One interesting point that can be captured here is all the studies showing a control test proving that the isolation method used for viruses is flawed. They can be listed as follows:

John F Enders, 1954 - Under other agents isolated during the study. "A second agent was obtained from an uninoculated culture of monkey kidney cells. The cytopathic changes it induced in the unstained preparations could not be distinguished with confidence from the viruses isolated from measles." It is highlighted here. Refer to the video explanation here.

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It is further discussed in the paper that "While there is no ground for concluding that the factors in vivo (in the body) are the same as those which underlie the formation of giant cells and the nuclear disturbances in vitro (outside a living organism), the appearance of these phenomena in cultured cells is consistent with the properties that a priori might be associated with the virus of measles.”

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Rustigian et al, 1955 - This paper is described in an article by Viroliegy here (look under Rustigain in the article).

Cohen et al, 1955 - This paper is also described in the same article by Viroliegy here (look under Cohen in the article).

Bech and von Magnus, 1959 - This paper is also described in the same article by Viroliegy here (look under Von Magnus in the article).

F Rapp et al, 1959 - This paper is described in a video by Spacebusters here. Most noteworthy is “Monkey kidney cells, however, are unsuitable for the investigations of the type reported here; Peebles et al. and Ruckle showed that monkeys, and cell cultures derived from them, are often infected with an agent serologically indistinguishable from human measles virus, which causes cytopathic changes in monkey kidney cell cultures almost identical with those caused by human measles virus.”

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Carl J. O’Hara et al, 1988 - The study demonstrated "HIV" particles in 18 out of 20 (90% of) AIDS-related lymph node enlargements but also in 13 out of 15 (88% of) non-AIDS-related enlargements. Which means that particles claimed to be HIV virions are non-specific since identical particles can be found in the majority of patients with enlarged lymph nodes not attributed to AIDS, and at no risk for developing AIDS. Refer to @Aldhissla45’s tweet here.

P Gluschankof et al, 1997 - This paper described in a video here with additional notes by Jamie here.

Julian W. Bess Jr., 1997 - This paper described in a video here with additional notes by Jamie here.

C.A. Cassol, 2020 - This paper is described by Andrew Kaufman here as well as by Thomas Cowan here.

“Unofficially” we can also add the Lanka 3 phase control experiment that can be seen here or searched for it here.

A further indication of the isolation procedure fallacy is shown in a study during which the CPE becomes more well defined with the addition of specific substances. The study is as follows:

Leon Caly et al, 2020 - “Following several failures to recover virions with the characteristic fringes of surface spike proteins, it was found that adding trypsin to the cell culture medium immediately improved virion morphology.” See a video explanation here.

Recent Requests and Statements

Further and more recent requests and statements that were sent to me by my good friend Courtenay are as follows:

May 5, 2022:
U.S. CDC and Agency for Toxic Substances and Disease Registry confirmed that a search of their records failed to find any that describe anyone on Earth finding an alleged “avian influenza virus” in the bodily fluids of any diseased diseased host (animal or human) and purifying “it”… which is necessary so that “it” could be sequenced, characterized and studied with controlled experiments. This can be viewed here.

May 20, 2022:
Public Health Agency of Canada confirmed that they have no record of any alleged “avian influenza virus” having been found and purified from the bodily fluid/tissue/excrement of any diseased “host” on the planet (in order for “it” to be sequenced, characterized and studied with controlled experiments) by anyone, anywhere, ever.
Insanely, they insist that:

“Viruses” are in hosts despite their utter inability to find them there,.

It’s necessary to “grow them” in non-host cells (as if “they” would grow better there than they allegedly grew in the diseased host lol).

They pretend that mixing complex substances together results in purification.

This can be viewed here.

December 20, 2021:
Public Health Agency of Canada confirmed that they have no record of any alleged “virus” having been purified from a sample taken from any diseased human on Earth, by anyone, ever, period. To be viewed here.

March 11, 2022:
U.S. Centers for Disease Control and Prevention and Agency for Toxic Substances and Disease Registry respond to a FOIA request for all studies / reports in their possession, custody or control describing the purification of any “virus” addressed by any “vaccine” on either their childhood or adult U.S. “immunization” schedule, directly from a sample taken from any diseased "host" on Earth where the sample was not first combined with any other source of genetic material. CDC/ATSDR provided 5 studies on “rotavirus” (thereby admitting they have no records for any other alleged viruses). None of these 5 studies actually describe isolation/purification of a “rotavirus” from a human.
Request, response, studies to be viewed here.

March 8, 2023:
Italy 2020: Inside Covid’s “Ground zero” in Europe - Three years ago the Western World came to a standstill. The official Covid-19 narrative depicted a strange suddenly-super-spreading, deadlier-than-flu virus hailing from China that landed in Northern Italy.

On February 20, 2020 the first alleged case of Covid-19 was discovered in the West in the Lombardy town of Codogno, Italy. Later that day the Italian government reported their first “Covid-19 death.”

Dramatic media reports emerging from Northern Italy were hammered into and onto the Western psyche giving the impression there was a mysterious “super spreading” and “super lethal” novel virus galloping across the region infecting and killing scores of people.

Read the rest of the report here.

Conclusion

The above list will be worked on over the coming years. If you think that any corrections need to be made or if you want to add additional studies, please leave a comment.


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