NewsCaster Ai Review | Build News Broadcasting Websites Like CNN, BBC & FoxNews


Brand New Ai App Powered by ChatGPT 4.2 That Builds Us 𝐒𝐞𝐥𝐟-𝐔𝐩𝐝𝐚𝐭𝐢𝐧𝐠 News 𝐁𝐫𝐨𝐚𝐝𝐜𝐚𝐬𝐭𝐢𝐧𝐠 𝐒𝐢𝐭𝐞𝐬 𝐢𝐧 𝐀𝐍𝐘 𝐍𝐢𝐜𝐡𝐞…𝐈n 𝐀𝐧𝐲 𝐋𝐚𝐧𝐠𝐮𝐚𝐠𝐞 𝐢𝐧 3𝟎 𝐒𝐞𝐜𝐨𝐧𝐝𝐬…

A web-based tool called NewsCaster AI was created to automate the development and administration of news websites. It gathers content from multiple sources (RSS feeds) and posts it on your website using artificial intelligence. This makes it possible to start a news website that consistently publishes new information without the need for human article writing.


Read More >>
https://dilip-review.com/newscaster-ai-review/


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NIST - Scientists modify common lab refrigerator to cool faster with less energy:

https://phys.org/news/2024-04-big-quantum-chill-scientists-common.html

#Refrigeration #PulseTubeRefrigerator #Refrigerator #PTR #AcousticOptimization #Efficiency #Cryogenics #Physics

EX-FEMINIST SPEAKS SOME TRUTH
https://www.bitchute.com/video/jF9wEkPWb34N/

'We broke into IDF, hold quarter of a million documents,' hacker group Anonymous claims.

Pro-Palestinian hackers allege that after penetrating the Justice Ministry, they now possess 20 gigabytes of data, including nearly a quarter-million documents related to the Israeli military.
https://www.jpost.com/international/article-797925

Why Do American Administrations Slave for Israel - VT Foreign Policy
Why Do American Administrations Slave for Israel? By Dr. Elias Akleh April 8th. 2024 Although the state of Israel was illegally founded by colonial …
http://donshafi911.business.blog/2024/04/15/why-do-american-administrations-slave-for-israel-vt-foreign-policy/

Why Do American Administrations Slave for Israel?
By Dr. Elias Akleh

April 8th. 2024

Although the state of Israel was illegally founded by colonial settler terrorist groups such as the Haganah, Irgun, and the Stern (Lehi) gangs, who started the still ongoing Palestinian Genocide 76 years ago in 1948 when they perpetrated hundreds of gruesome massacres against Palestinian civilians, detonated to the grounds hundreds of Palestinian towns and villages, and bulldozed thousands of fertile fields uprooting thousands of tens of hundreds yeas old olive and orange trees to build their illegal settler colonies, successive American administrations had blindly and obediently slaved for maintaining and strengthening this illegal presence in the middle of the Arab world.

A ROCKEFELLER INSIDER GIVES A RARE GLIMPSE OF THE REAL REASONS FOR THE FEMINIST MOVEMENT. "ONE REASON
https://www.bitchute.com/video/vxDgOKuEuPru/

Pro-Palestinian Hackers Claim Massive Data Breach of Israeli Ministry https://www.thehackerwire.com/pro-palestinian-hackers-claim-massive-data-breach-of-israeli-ministry/

The President of the ICJ Joan E. Donoghue was a legal advisor to Secretary of State Hillary Clinton under the Obama administration. Joan Donoghue takes her instructions from Washington.

Moreover, the conduct of the genocide is a joint Israel-US endeavor with US forces involved in Israel’s combat units.

Nobody in the media nor in the peace movement has underscored the fact that the President of the ICJ is de facto in “conflict of interest”.

“The anger of the World has been pacified for a while with the false celebration of a fake “victory” at The Hague. The US chief judge at ICJ must be laughing.

Israel’s genocide will continue while the US and its chief justice at the ICJ keep the world at bay for very long with new false words and delaying actions.” (Karsten Riise, Global Research emphasis added)


http://donshafi911.blogspot.com/2024/04/fake-justice-at-hague-icj-appoints.html https://donshafi911.blogspot.com/2024/04/fake-justice-at-hague-icj-appoints.html?m=1

What is significant is that the German Health authorities based on official data have now been obliged under Freedom of Information to reveal the devastating nature and impacts of the Covid lockdowns imposed on 190 countries, starting March 11, 2020.

Most of the independent studies including those conducted by Global Research have been the object of censorship.

Of Significance, the official documents of the Germany’s Ministry of Health consistent with the independent reports published in the course of more than 4 years pertaining to the COVID-19 lockdowns, the mandatory wearing of the face mask, and the experimental mRNA vaccines.


http://donshafi911.blogspot.com/2024/04/bombshell-official-data-from-germanys.html

The third Guest Artist Recital of The U.S. Army Band 2024 American Trombone Workshop featured Jeff Gittleson & Alex Felker playing Angel's Tango by Steven Verhelst, SSG Kyle Price & SSG Michael Burner playing Red Spain by Nicola Ferro, Matthew Ethier & pianist Topher Ruggiero playing Thoughts of Love by Arthur Pryor, and John Gruber & pianist Topher Ruggiero playing Romance by William Grant Still. #ArmyMusic #OberlinCollege #Oberlin #BassTrombone #Trombone #ATW #ATW2024 #Music

The U.S. Army Blues featured jazz trombonist Steve Turre, who was joined for a finale by Altin Sencalar and the winners of the National Jazz Solo Competition, Pablo Muller Santiago & Jackson Churchill, at The U.S. Army Band 2024 American Trombone Workshop. #SanctifiedShells #Shells #ArmyBlues #MilitaryMusic #JazzTrombone #Jazz #Trombone #ATW2024 #ATW #Music

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

0:21

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

0:25

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

0:33

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

4:02

and what happens when we want to control a process

4:06

that's beyond our capabilities as humans

4:08

we just connect this process to a computer

4:10

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

4:19

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.

5:05

So we might not need even new drugs.

5:07

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...

5:13

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?"

5:21

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.

5:30

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

5:34

which is DNA.

5:36

And in fact every part of the robot,

5:38

every part of out nanorobots:

5:40

Moving parts, axis, locks, chasis, software,

5:44

everything is made from DNA molecules.

5:46

And the techonology that enables us to do this

5:49

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

5:52

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.

5:59

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.

6:08

For example these shapes, so these are actual microscopic images

6:12

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

6:16

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

6:19

are a hundred nanometers in size

6:21

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

6:24

Now since 2006 several researchers, really talented ones,

6:28

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

6:32

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

6:35

using this technique.

6:36

And these researchers also gave us computer-aided design tools

6:41

that enable everyone

6:43

very very simply to design objects from DNA

6:46

So these CAD tools amazingly

6:49

enable us to focus o n the shape we want

6:52

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

6:57

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

7:02

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

7:05

is a spreadsheet with fragments of DNA

7:08

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

7:11

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

7:16

several days later to your doorstep

7:18

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

7:23

and these molecular bricks will self-assemble into

7:26

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

7:30

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

7:34

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

7:38

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

7:42

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

7:45

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

7:49

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

7:54

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

7:57

and the nanobot can be programmed to turn on and off

8:01

these functions at certain places and at certain times

8:05

this is how we control those molecules

8:07

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

8:16

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

8:18

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,

8:37

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

8:42

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

8:47

any cargo inside is now accessible,

8:49

it can attack target cells or target tissues

8:52

or other robots which you'll see later on.

8:54

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

8:58

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

9:02

We can control which payload becomes accessible at which time point

9:05

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

9:12

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

9:19

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

9:29

nothing happens, no cell is affected, because the robot

9:32

safely sequesters those drugs inside.

9:35

When we unlock the robots

9:37

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

9:42

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

9:46

to help us see better the output.

9:48

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

10:12

and my team keeps expanding this range monthly.

10:17

So these are nanorobots and to another topic

10:22

organisms in nature, like bacteria and animals

10:26

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

10:34

and since we are interested in

10:36

very complex medical procedures, very complex therapeutic settings,

10:40

we're wondering what we could do

10:42

if we could engineer artificial swarm behaviors

10:46

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

10:51

Can we teach them to behave like animals, like insects

10:55

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

11:04

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

11:12

this is virtually impossible, it's impractical

11:15

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

11:23

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

11:27

and you let the behaviours emerge from that group

11:31

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

11:35

for example, just as ants

11:38

can shake hands and form physical bridges between two trees

11:42

or two remote parts of the same tree,

11:44

we already have nanorobots that can reach out for each other

11:47

touch each other and shake hands in such a way

11:49

they form physical bridges.

11:51

Then you can imagine these robots

11:53

extending, making bridges extending from one-half

11:56

to the other half of an injured tissue,

11:58

an injured spinal cord for example

12:00

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

12:03

and once they stretched over that tissue gap

12:06

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

12:10

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

12:14

So we already did that and...

12:17

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

12:21

and this is amazing because as you can see here

12:24

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

12:28

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

12:32

while "B" is not and viceversa.

12:34

So this is good for combination therapy

12:36

with combination therapy we take multiple drugs, right?

12:39

and sometimes two or more of these drugs

12:41

can collide and generate side effects,

12:43

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

12:46

and the robots will time the activities so that

12:49

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

12:52

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

12:57

Another example that we did is the quorum sensing.

13:00

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

13:05

It means nanorobots can count themselves

13:08

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

13:12

this is a mechanism invented by bacteria in evolution

13:15

and they regulate amazing behaviours based on just their population density

13:18

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

13:23

so our robots can count themselves and switch to on

13:26

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

13:29

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

13:33

to become active only when reaching a certain dose

13:36

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

13:41

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

13:43

so this nanobots can do computing.

13:45

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

13:48

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

13:53

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

13:58

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

14:02

and these logic gates are set to interact to produce computations

14:05

so we can also produce computation by setting interactions between nanorobots

14:10

to emulate logic gates like you see here

14:13

and they form chains and they form pairs

14:15

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

14:19

of computing based on interacting nanorobots

14:22

and to prototype these

14:24

we are using animals, very interesting animals

14:27

these are cockroaches,

14:28

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

14:30

they're actually from South America

14:32

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

14:35

[Laughter]

14:36

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

14:40

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

14:43

have you ever tried putting cockroach to sleep?

14:46

We put in the freezer for seven minutes

14:48

in they fall asleep

14:49

and we can inject these nanorobots inside

14:52

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

14:55

And those robots

14:57

while they're doing this, the robots read molecules

14:59

from the cockroaches' inputs

15:01

and they write their outputs in the form of drugs

15:04

activated on those cockroaches' cells

15:06

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

15:09

architectures of interecting nanorobots that can emulate logical operators

15:14

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

15:25

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

15:30

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

15:33

of an 8-bit computer like Commodore 64.

15:36

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

15:40

my team [has] developed nanorobots that carry antennae

15:44

these antennae are made from metal nano-particles.

15:47

Now, the antennae enable the nanobots

15:49

to respond to externally applied electromagnetic fields

15:52

so these nanorobots, this version of nanobots

15:55

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

15:58

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.

16:11

For example you can imagine nanorobots being injected

16:14

to Dana, my daughter for example,

16:16

and the doctor can guide those robots

16:19

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

16:23

And you can already see an example where we actually took

16:26

cancer cells and loaded robots with cancer drugs

16:29

and activated the drug by a hand gesture.

16:31

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

16:34

as you can see here.

16:36

And the interesting thing is that

16:39

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

16:44

the controller actually links those nanobots to the network

16:47

so they have an actual IP address

16:49

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

16:53

for example, my doctor's smartphone

16:55

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

17:04

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

17:08

has their own unique molecular signature

17:11

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

17:15

and if you know these molecules

17:17

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

17:21

and you can program them to look for bits,

17:23

this could be for example signally molecules between cells,

17:26

and either fetch them for diagnostics

17:28

or carry them to different addresses.

17:30

And we already have robots that can hijack

17:33

signals between cells

17:34

and manipulate an entire network of communications between cells

17:37

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

17:43

communicate and orchestrate to perpetuate a disease.

17:46

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.”

https://outraged.substack.com/p/the-emergence-of-nanobot-society?utm_source=cross-post&publication_id=1087020&post_id=143145132&utm_campaign=956088&isFreemail=true&r=1sq9d8&triedRedirect=true&utm_medium=email

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

CASE 01 - Autopsy proven myocarditis death in AUSTRALIA
Barrack Heights NSW, AUSTRALIA - Roberto Garin was only 52 when he ‘died suddenly’ on 28 July 2021. The healthy father of two teenagers began feeling ill 48 hours after his first Pfizer shot and dropped dead in front of his terrified wife Kirsti six days later while she was on the phone to paramedics.
Garin’s family immediately suspected the vaccine caused his death. Kirsti was told her husband was the first person to die after a Pfizer shot. In fact, 176 deaths following Pfizer jabs had already been reported to the Therapeutic Goods Administration (TGA), starting in the first week of the vaccine rollout.
But when Kirsti shared her concerns with filmmaker Alan Hashem, who released the video together with the accounts of other vaccine injuries and deaths, it unleashed a storm.
‘Misinformation researchers’ published by the ABC dismissed Kirsti’s ‘claims her 52-year-old husband died from “sudden onset myocarditis” after receiving the Pfizer vaccine’ because it didn’t ‘square with official data’.
Yet that was exactly what forensic pathologist Bernard l’Ons wrote in a brilliant report on his autopsy stating that the deceased’s heart showed a clear transition to severe giant cell myocarditis that could be ‘histologically dated to the time period of the Covid-19 mRNA vaccination’ and it was ‘reasonable to state that the deceased’s previously undiagnosed cardiac sarcoidosis may have transitioned to a fulminating myocarditis as a result of the Pfizer Covid-19 vaccination’ noting that myocarditis had been reported in reactions to the Pfizer vaccine. L’Ons proposed a mechanism by which the vaccine could trigger fatal myocarditis and advised that a possible therapeutic implication was that sarcoid patients be given an echocardiogram to detect whether their heart was affected in which case alternative vaccination types could be considered.
All of this was ignored by the TGA which refuses to admit to this day that any death can be attributed to a Pfizer vaccine and was parroted by the ABC. The TGA did admit that as of 22 August it had received ‘235 reports of suspected myocarditis, (inflammation of the heart muscle) and/or pericarditis (inflammation of the membrane around the heart) following vaccination’ with Pfizer but said, ‘These reports reflect the observations of the people reporting them and have not been confirmed as having been caused by the vaccine,’ and that ‘some events may be coincidental and would have happened anyway, regardless of vaccination.’
This is a particularly misleading statement. Four out of five reports to the TGA are submitted not by random ‘people’, but by highly qualified health professionals and in Garin’s case by a forensic pathologist.
Why would the TGA dismiss these reports? That’s a question Associate Professor Michael Nissen could perhaps shed light on. He was appointed to the TGA in February 2021, just as the Covid-19 vaccines were rolled out, to lead its Signal Investigation Unit which investigates safety issues that arise with vaccines in adverse reports or are raised by international regulators or the medical literature.
Prior to his appointment, Nissen was the Director of Scientific Affairs and Public Health at GSK Vaccines from October 2014 to January 2021, a period during which GSK and Pfizer entered into a joint venture. Nissen worked concurrently in hospital-based medical care and academia. He has led over 40 clinical trials and authored over 200 peer-reviewed publications including vaccine studies. In all these areas pharmaceutical companies are a major source of funding.
The TGA is sensitive about managing conflicts of interest for advisory committee members but offers no guidance on its website with regard to staff members although presumably the same principles should, at least in theory, apply. It notes that shares, involvement in clinical trials, employment, contracts, consultancies, grants, sponsorships, board memberships and so on, may give rise to a conflict of interest.
Robert Clancy, an Emeritus Professor of Pathology at the University of Newcastle Medical School and a member of the Australian Academy of Science’s Covid-19 Expert Database wrote in Quadrant online last week that ‘the power of the pharmaceutical industry and its pervasive influence at every level of political and medical decision-making’ has been underestimated in shaping the pandemic narrative which has been driven by commercial imperatives to such an extent that it has crushed scientific debate.
Clancy recounts that his approach to the College of Pathology (of which he was a Senior Fellow, a foundation Professor of Pathology, and past-Chairman of the College committee for undergraduate pathology education) calling for a national study to determine whether Covid vaccination was responsible for the increase in excess mortality in Australia and elsewhere by developing a protocol for post-mortems ‘to answer what is arguably the most important question facing medicine’ met with a rejection and a suggestion to take it instead to the TGA.
Nowadays, dying suddenly has become ominously familiar. According to a new film Died Suddenly available as of this week to stream via Twitter, in the last 18 months, the term ‘Died Suddenly’ has risen to the very top of ‘most searched’ Google terms. The film documents the surge in excess mortality in highly vaccinated countries. Dr. Peter McCullough, internist, cardiologist, epidemiologist, and one of the top five most-published, and most censored, medical researchers in the US, says that sudden death frequently occurs because the heart has been damaged by inflammation caused by Covid vaccines.
Papers that Pfizer and the Food and Drug Administration tried to hide for 75 years show that Pfizer knew in 2020 that myocarditis and pericarditis could be caused by its vaccine.
And in the Pfizer trial in Argentina, a report on a healthy 36-year old  participant – Augusto German Roux – who developed pericarditis immediately after his second Pfizer jab, mysteriously disappeared from the published trial results.
The Australian Technical Advisory Group on Immunisation (ATAGI) and the Cardiac Society of Australia and New Zealand (CSANZ) belatedly published a warning about myocarditis and pericarditis in September this year.
It was too late for Garin. Had his doctors known, his life might have been saved. His grieving family have still not received a cent in compensation. But Pfizer has apparently grossed nearly $100 billion from its sales of Covid-19 vaccines and treatments.
Rebecca Weisser is an independent journalist.
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https://open.substack.com/pub/makismd/p/mrna-injury-stories-australian-dad?r=29hg4d&utm_medium=ios