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I see a lot of patients who have been harmed by COVID and the shots.

What I rarely see is anyone who was exposed to the spike protein but still feels perfectly fine: just here for a checkup, doc!

Most of my patients did feel perfectly fine for weeks, months and sometimes years after their spike protein exposure, before suddenly coming down with severe symptoms.

But in these cases there was ongoing inflammation, spike persistence, perhaps viral persistence, micro clotting, perhaps autoimmunity, alterations in gut bacteria and more that could have been detected far sooner.

This is important because it's always easier to prevent illness than to treat illness once it manifests.


http://donshafi911.blogspot.com/2024/04/so-you-got-spiked-now-what-especially.html

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.
======


https://open.substack.com/pub/makismd/p/mrna-injury-stories-australian-dad?r=29hg4d&utm_medium=ios

So You Got Spiked: Now What?
Especially important for athletes and future parents: invest in your health, your future & future generations.

Dr. Syed Haider
Spikehead | Niskia | Flickr
I see a lot of patients who have been harmed by COVID and the shots.

What I rarely see is anyone who was exposed to the spike protein but still feels perfectly fine: just here for a checkup, doc!

Most of my patients did feel perfectly fine for weeks, months and sometimes years after their spike protein exposure, before suddenly coming down with severe symptoms.

But in these cases there was ongoing inflammation, spike persistence, perhaps viral persistence, micro clotting, perhaps autoimmunity, alterations in gut bacteria and more that could have been detected far sooner.

This is important because it's always easier to prevent illness than to treat illness once it manifests.

Thank you for reading Dr. Syed Haider. This post is public so feel free to share it.

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It takes a lot to push your body out of health and often takes a lot to push your body back into the fully resilient state of health you were in before.

This is contrasted with symptomatic, or functional recovery - with Long Haul it’s often relatively easy to get someone back to feeling 90-100% better while they are taking treatments like ivermectin and making some lifestyle changes.

What is harder is to get them back to the place of resilience they were at before they got sick: able to eat whatever they want, sleep whenever they want, get by without supplements and meds, etc.

I certainly believe it is possible and it does happen, but that complete healing is a harder nut to crack than simply functional recovery dependent on various “crutches”.

Obviously part of complete and deep healing is making the often drastic lifestyle changes - because it was the poor lifestyle that got you in trouble in the first place, along with toxic exposures from the environment and food.

So ultimately you don’t really want to return to the way things were before you got sick: that would just set you up to get sick all over again.

This is confusing for people, because they thought they were fine.


I hear this repeatedly: I was so healthy before COVID (or the shot).

But when I push a bit it's clear patients were not sleeping enough, were overtraining, under too much stress, having too much caffeine/alcohol, not getting enough sun, spending too much time indoors, online, in front of screens, eating relatively poorly, consuming too many pesticides, seed oils, had leaky gut, autoimmune issues, skin issues, etc.

Many patients list no medical problems yet also list a number of medications for psychiatric diseases, hypertension, cholesterol, migraines, erectile dysfunction, etc. We’re hardwired to minimize things, to ignore them and to forget them.

Our culture trains us to have high time preference: meaning we prefer the present too much compared to the future.

Most people are depleting their reserves instead of building them. Just as most find it difficult to save money or invest for the future, most also find it difficult to invest in their health with exercise, sleep, sun, diet, etc.


The millionaire who eats through their savings rather than investing it can live high on the hog for a few years, but eventually the millions run out and then they’re left with nothing.

The same happens with our health: youth and health usually go hand in hand and they are a form of wealth that can be used up before its time, or can be conserved and built upon so that it lasts for the long term.

So the first thing everyone must do is clean up their act and start investing in their future. The most important wealth is health.

Second, anyone who got the shot and thinks they are fine, should still consider doing something to check themselves out: there is a lab panel I order at mygotodoc.com that can be done at a local lab and may be covered by insurance.

Register Free at mygotodoc

There are more advanced panels we can send to Incelldx to check for spike protein in monocytes and for advanced inflammatory markers. There is an atypical amyloid fibrin microclot score we can order from a specialized pathology lab, and there is Dr Sabine Hazan’s gut microbiome testing that I can order via Progenabiome.

There are some supplementary tools as well like tracking heart rate variability, sleep quality, and continuous glucose monitoring that is especially important for those with poor metabolic health, which is most people nowadays.

Athletes might especially consider cardiac screening with troponin, BNP, EKG, Echo and perhaps even a cardiac MRI: when sudden death is a possibility even seemingly excessive screening may become sensible.

Doctors Taking ER Call: A Dying Breed
But the population I worry the most about are women in their reproductive years. Dr James Thorp has spoken out about this at length in interviews and peer reviewed papers. Totality of the Evidence compiles the data currently available.

A baseline pre-pandemic miscarriage rate around 12% is already too high and data suggests it has shot up after the vax rollout. VAERS miscarriage reports spiked 4070% post shots. The initial Pfizer trial suggested a rate above 80% based on incomplete data, though it was misreported at the time by using the wrong denominator to hide the alarm.

I know what it feels like to lose a baby. It tears your heart out. It’s difficult to forgive yourself for perceived mistakes that may have triggered the pregnancy loss.

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Before pregnancy is a time to build your resources: focus on supercharging your nutrient stores. Eat organ meats, eggs, steak, milk and avoid junk food: no seed oils or sugar and avoid pesticides. Consider plasma donation to cut down body stores of toxic chemicals. Optimize sleep, sun, stress management, body fat levels, and metabolic health. Generally aim to get into the best shape of your life.

And if you were exposed to spike protein check to see if you need to detox from it.

You can eliminate spike and microclots and inflammation and even autoimmunity triggered by the shots or COVID.

If you don’t deal with it before pregnancy you may have to deal with it during pregnancy in the form of long haul or worst case scenario a pregnancy loss triggered by spike, and even after birth your baby may be harmed via spike in breast milk.

There is a report in VAERS of a breastfed baby dying soon after its mothers got the shot:

One report doesn’t mean it’s only happened once. VAERS is severely underreported, especially for these shots.

We should heed the warnings Pfizer gave male trial participants not to go near pregnant women and if having sex with women of childbearing age, to use at minimum two forms of contraception.

If anything we have far more data now than we did then to suggest that spike protein exposure is unsafe for everyone and especially those pregnant or breastfeeding.

Many of my female patients report altered menstrual cycles and other symptoms whenever they are exposed to those recently vaccinated.

Shedding is a real phenomenon and it can wreak havoc on the female reproductive system.

Whether or not there is a depopulation agenda we are seeing a dramatic worldwide drop in live birth rates.

Sperm counts have dropped, female fertility is at all time lows, and miscarriage rates have shot up.

There are simple solutions that can accomplish short term goals of fertility and symptom relief and there are more comprehensive lifestyle based solutions that solve the underlying problems for the long term.

Free Lifestyle Ebook/Webinar/Course

Invest in yourself and your children for the long run and you won’t be sorry.

https://blog.mygotodoc.com/p/so-you-got-spiked-now-what

https://telegra.ph/So-You-Got-Spiked-Now-What-04-02

More Proof mRNA Shots Edit Human Genome
New Study Again Shows LINE-1 "Junk DNA" Does The Dirty Work

Dr. Syed Haider
Could the mRNA shots edit germline DNA?
Honest scientists have always been worried about retrointegration of foreign mRNA from “vaccine” shots into our own cellular DNA.

This fear should have been allayed by rigorous genotoxicity safety studies before the mRNA shots where rolled out, but those studies were waived by the Big Pharma controlled FDA (with the DoD behind the scenes pulling all the strings).

Previous research showed that this could theoretically occur in a human liver cancer cell line inside a controlled laboratory setting utilizing our own bodies reverse transcriptase enzymes that are upregulated in cancer cells.

Naysayers still argued that this situation was impossible or at least extremely unlikely to occur in our bodies.

Unfortunately there is now further proof that this really does occur, either right away after vaccination, or if not, then it’s even more likely to occur once a vaccinated individual catches COVID-19, as long as vaccinal mRNA remains present in the body (so far we know it remains in circulation for weeks and in the lymph nodes for months - likely far longer, since all the studies had to be stopped, presumably due to lack of funding, or out of fear of creating unpublishable papers since the news wasn’t looking good).

Thank you for reading Dr. Syed Haider. This post is public so feel free to share it.

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A new paper by Zhang et al, just released on Feb 13, 2023 proves that at artificially high concentrations in a lab setting, the SARS-CoV-2 virus can retrointegrate into our genome.

Thankfully during natural infection such high levels of viral RNA do not typically occur, but … (you knew there had to be a “but”)

… such high levels are induced by mRNA vaccination.

So what the paper may actually prove in the roundabout way of most modern research (required for publication to ever happen in todays politically charged Big Pharma controlled publishing environment) is that the mRNA in the shots is in fact likely to retrointegrate into our cellular DNA.

To dig into the details we need to start with a quick basic bio refresher:

Understanding Genetics
Nearly every cell in our bodies carries a full copy of our genetic code, or genome (the exceptions are red blood cells that have no genome, and sperm and egg cells that have half a genome since they are meant to combine with half of someone else's genome).

Our genome is made up of individual genes encoded by DNA and bundled together into 46 chromosomes that are stored in a central compartment of our cells called the nucleus.

In order to “read" the DNA code and convert it into the structure that makes up our bodies, it is first translated by a “reader” protein that writes it out into a new free floating molecule called mRNA for messenger RNA (the mRNA shots carry this messenger RNA, not modified RNA as some people think).

The mRNA, unlike the DNA is not stuck inside the chromosome and it can exit the nucleus, going into the larger compartment called the cytoplasm of the cell, where its message is “read” and translated into an amino acid sequence that folds itself into a protein (either a body protein, or in the case of the shots the spike protein, or in the case of an RNA virus infection like SARS-CoV-2, all the proteins of the virus).

Now going back to the nucleus: some of the individual DNA encoded genes can move around within their chromosomes and have therefore been described as "jumping genes" or technically speaking: transposable elements (TEs).

Jumping genes!
Some of these jumping genes (Class 1 TEs) use a copy and paste mechanism and others (Class 2 TEs), like the one in the cartoon depiction above, use a cut and paste mechanism.

The Class 1 TEs (AKA retrotransposons) that use the copy and paste mechanism do so by translating their DNA into RNA and then converting the RNA back into DNA and inserting it somewhere else in the genome.

The Class 1 TEs or retrotransposons, include within themselves the genetic code necessary to create their own protein enzyme to convert the DNA back into RNA, which is termed reverse transcriptase.

Fun fact: retroviruses like HIV can be considered a special subtype of retrotransposon that can not only reinsert inside the same cell, but also travel to other cells “infecting” them and reverse transcribing into their genomes.

In humans the only active jumping genes are from CLASS 1 TEs/retrotransposons and are called LINE-1 retrotransposons (LINE stands for Long Interspersed Nuclear Elements).

LINE-1 retrotransposons were once considered to be junk DNA, they are usually inactivated, but can be turned on in aging cells, cancer cells, virus infected cells and in general in any cell subjected to significant stress.

Junk DNA, which makes up 98.5% of our genome, is still little understood. It may help regulate the activity of the other 1.5% of the genome that does code for proteins, is likely involved in genome evolution, and has been implicated in disease states like cancer, autism and dozens of genetic diseases.

So, what’s been shown in this new paper by Zhang et al, is that a lab clone of the SARS-CoV-2 virus, when present in very high levels, does turn on LINE-1, which means it also turns on the LINE-1 reverse transcriptase enzyme, which it then makes use of to reverse transcribe itself into our DNA.

But even worse: genome sequencing found the viral genetic code transcribed into our DNA not only in cells where LINE-1 was actively turned on, or overexpressed above baseline, but even in cells where it was not.

Is Sangamo's Gene-Editing Approach a Bust? | The Motley Fool
Then, instead of studying the LNPs and spike protein RNA used in the shots, the researchers (who valued their careers) used a different mechanism of delivering low levels of nucleocapsid RNA into the cells in the lab to see if they also up regulated LINE-1 expression and were integrated into the cellular DNA.

Turns out this handicapped experiment did not up regulate LINE-1, or get taken up in detectable quantities by healthy cells, though it did lead to genomic uptake in cells that already had LINE-1 upregulated - which again happens in aging cells, cancer cells, virus infected cells or simply in cells under stress (perhaps from LNP and spike protein induced inflammation?).

The study authors addressed the discrepancy in retrointegration between the viral clone and their handicapped version of an mRNA shot by theorizing there were:

"...several possible explanations for the differences in the levels of retrotransposition in infected and transfected cells: (i) The relative abundance of viral RNA is almost 2 orders of magnitude higher in infected than in transfected cells which would increase the probability of association with LINE1 proteins; (ii) virus infection, but not viral mRNA transfection, can induce endogenous LINE1 expression; (iii) multiple factors during SARS-CoV-2 infection can inhibit the antiviral/anti-retrotransposition function of stress granules (48–53), which could increase retrotransposition.”

The first theory is the most concerning.

Based on what we know from a 2020 study by Xie et al that showed the very high levels of intracellular viral RNA achieved by infectious clones, we can extrapolate that in the current study by Zhang et al the concentration of mRNA achieved by the SARS-CoV-2 viral clone was likely about 1000X greater than the low levels typically found during a natural infection.

In fact the levels of mRNA in each cell achieved by the viral clone in the current study are actually far more likely to be achieved by transfection into cells of LNPs in the shots carrying spike protein mRNA than they are during a natural infection.

Life finds a way. - Reaction GIFs
So if the authors first theory is correct, that the difference in retrointegration rates simply depends on the intracellular concentration of foreign RNA, then retrointegration is very likely to occur due to exposure to mRNA in the shots, and it is likely to dramatically increase in case someone who has received the shot later becomes infected by the SARS-CoV-2 virus - since we know it upregulates LINE-1 expression, or if they are put under other stressors including the development of cancer, or by the stress of long COVID, chronic vaccine injury, autoimmune disease, autonomic dysfunction, POTS, MCAS, etc - all of which are also sadly enough triggered by the shot.

This is less likely to happen in germ cell DNA - our sperm and egg cells - and lets hope it doesn’t happen, since we already know that the shots likely do transmit altered immunity from mother to child, if they also pass on the mRNA coding the spike protein itself then huge swaths of humanity may be forever genetically altered.

Heres hoping the label “junk DNA” actually applies in this case…

But, if you’ve been vaccinated: don’t worry!

At mygotodoc we routinely reverse vaccine injuries and sincerely believe every disease has a cure.

Fear is more likely to kill you than the shot (but do stop getting the boosters), and I mean that literally: fear destroys the immune system.

A healthy immune system can keep any illness in check even if from a retrointegrated virus or viral mRNA fragment.

There are a lot of unknowns, but don’t let that scare you. Take your health into your own hands and start making positive changes today.

https://blog.mygotodoc.com/p/more-proof-mrna-shots-edit-human


https://telegra.ph/More-Proof-mRNA-Shots-Edit-Human-Genome-09-17-2

BEWARE!

Epoch Times is now promoting Aspirin from a government study which says that Aspirin "may" reduce liver fat.

Calling it "Baby Aspirin” is a clever way of making it sound harmless but do not be deceived!

👉A NBC News report from 2011 revealed internal leaked documents proving that the pharmaceutical ingredients in Bayer Aspirin induce autoimmunity!

https://www.youtube.com/watch?v=XOp5mTmAUr8&embeds_referring_euri=https%3A%2F%2Ftwitter.com%2F&source_ve_path=Mjg2NjY&feature=emb_logo

And a study from 2019, also reported by NBC, further confirmed that a seemingly harmless "one Aspirin per day" is not only harmful to health but also does NOT prevent heart attacks or cardiovascular disease!

https://www.youtube.com/watch?v=X0x7uI_SYBE&embeds_referring_euri=https%3A%2F%2Ftwitter.com%2F&source_ve_path=Mjg2NjY&feature=emb_logo

Meta Refuses to Answer Questions on Gaza Censorship, Say Sens. Warren and Sanders
Sam BiddleMarch 26 2024, 8:00 a.m.
WASHINGTON, DC - MARCH 03: Sen. Elizabeth Warren (D-MA) questions U.S. Federal Reserve Chair Jerome Powell as he testifies at a Senate Banking, Housing, and Urban Affairs Committee hearing on the Fed's "Semiannual Monetary Policy Report to the Congress," on Capitol Hill on March 3, 2022 in Washington, DC. (Photo by Tom Williams-Pool/Getty Images)
Citing the company’s “failure to provide answers to important questions,” Sens. Elizabeth Warren, D-Mass., and Bernie Sanders, I-Vt., are pressing Meta, which owns Facebook and Instagram, to respond to reports of disproportionate censorship around the Israeli war on Gaza.

“Meta insists that there’s been no discrimination against Palestinian-related content on their platforms, but at the same time, is refusing to provide us with any evidence or data to support that claim,” Warren told The Intercept. “If its ad-hoc changes and removal of millions of posts didn’t discriminate against Palestinian-related content, then what’s Meta hiding?”

In a letter to Meta CEO Mark Zuckerberg sent last December, first reported by The Intercept, Warren presented the company with dozens of specific questions about the company’s Gaza-related content moderation efforts. Warren asked about the exact numbers of posts about the war, broken down by Hebrew or Arabic, that have been deleted or otherwise suppressed.

The letter was written following widespread reporting in The Intercept and other outlets that detailed how posts on Meta platforms that are sympathetic to Palestinians, or merely depicting the destruction in Gaza, are routinely removed or hidden without explanation.

A month later, Meta replied to Warren’s office with a six-page letter, obtained by The Intercept, that provided an overview of its moderation response to the war but little in the way of specifics or new information.

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“Meta’s lack of investment to safeguard its users significantly exacerbates the political situation in Palestine and perpetuates tech harms on fundamental rights in Palestine and other global majority countries, all while evading meaningful legal accountability,” Mona Shtaya, nonresident fellow at the Tahrir Institute for Middle East Policy, told The Intercept. “The time has come for Meta, among other tech giants, to publicly disclose detailed measures and investments aimed at safeguarding individuals amidst the ongoing genocide, and to be more responsive to experts and civil society.”

Meta’s reply disclosed some censorship: “In the nine days following October 7, we removed or marked as disturbing more than 2,200,000 pieces of content in Hebrew and Arabic for violating our policies.” The company declined, however, to provide a breakdown of deletions by language or market, making it impossible to tell whether that figure reflects discriminatory moderation practices.

Much of Meta’s letter is a rehash of an update it provided through its public relations portal at the war’s onset, some of it verbatim.

Now, a second letter from Warren to Meta, joined this time by Sanders, says this isn’t enough. “Meta’s response, dated January 29, 2024, did not provide any of the requested information necessary to understand Meta’s treatment of Arabic language or Palestine-related content versus other forms of content,” the senators wrote.

Both senators are asking Meta to again answer Warren’s specific questions about the extent to which Arabic and Hebrew posts about the war have been treated differently, how often censored posts are reinstated, Meta’s use of automated machine learning-based censorship tools, and more.

Accusations of systemic moderation bias against Palestinians have been borne out by research from rights groups.

“Since October 7, Human Rights Watch has documented over 1,000 cases of unjustified takedowns and other suppression of content on Instagram and Facebook related to Palestine and Palestinians, including about human rights abuses,” Human Rights Watch said in a late December report. “The censorship of content related to Palestine on Instagram and Facebook is systemic, global, and a product of the company’s failure to meet its human rights due diligence responsibilities.”


Related

Meta Considering Increased Censorship of the Word “Zionist”

A February report by AccessNow said Meta “suspended or restricted the accounts of Palestinian journalists and activists both in and outside of Gaza, and arbitrarily deleted a considerable amount of content, including documentation of atrocities and human rights abuses.”

A third-party audit commissioned by Meta itself previously concluded it had given the short shrift to Palestinian rights during a May 2021 flare-up of violence between Israel and Hamas, the militant group that controls the Gaza Strip. “Meta’s actions in May 2021 appear to have had an adverse human rights impact … on the rights of Palestinian users to freedom of expression, freedom of assembly, political participation, and non-discrimination, and therefore on the ability of Palestinians to share information and insights about their experiences as they occurred,” said the auditor’s report.

In response to this audit, Meta pledged an array of reforms, which free expression and digital rights advocates say have yet to produce a material improvement.

In its December report, Human Rights Watch noted, “More than two years after committing to publishing data around government requests for taking down content that is not necessarily illegal, Meta has failed to increase transparency in this area.”

Update: March 26, 2024, 1:11 p.m. ET
This story has been updated to include a statement received after publication from Mona Shtaya, a nonresident fellow at the Tahrir Institute for Middle East Policy.

https://theintercept.com/2024/03/26/meta-gaza-censorship-warren-sanders/

The Silent Shame of Health Institutions
J.R. Bruning
For how much longer will health policy ignore multimorbidity, that looming, giant elephant in the room, that propagates and amplifies suffering? For how much longer will the ‘trend’ of increasing diagnoses of multiple health conditions, at younger and younger ages be rendered down by government agencies to better and more efficient services, screening modalities, and drug choices?

Multimorbidity, the presence of many chronic conditions, is the silent shame of health policy.

All too often chronic conditions overlap and accumulate. From cancer, to diabetes, to digestive system diseases, to high blood pressure, to skin conditions in cascades of suffering. Heartbreakingly, these conditions commonly overlap with mental illnesses or disorders. It’s increasingly common for people to be diagnosed with multiple mental conditions, such as having anxiety and depression, or anxiety and schizophrenia.

Calls for equity tend to revolve around medical treatment, even as absurdities and injustices accrue.

Multimorbidity occurs a decade earlier in socioeconomically deprived communities. Doctors are diagnosing multimorbidity at younger and younger ages.

Treatment regimens for people with multiple conditions necessarily entail a polypharmacy approach – the prescribing of multiple medications. One condition may require multiple medications. Thus, with multimorbidity comes increased risk of adverse outcomes and polyiatrogenesis – ‘medical harm caused by medical treatments on multiple fronts simultaneously and in conjunction with one another.’

Side effects, whether short-term or patients’ concerns about long-term harm, are the main reason for non-adherence to prescribed medications.

So ‘equity’ which only implies drug treatment doesn’t involve equity at all.

Poor diets may be foundational to the Western world’s health crisis. But are governments considering this?

The antinomies are piling up.

We are amid a global epidemic of metabolic syndrome. Insulin resistance, obesity, elevated triglyceride levels and low levels of high-density lipoprotein cholesterol, and elevated blood pressure haunt the people queuing up to see doctors.

Research, from individual cases to clinical trials, consistently show that diets containing high levels of ultra-processed foods and carbohydrates amplify inflammation, oxidative stress, and insulin resistance. What researchers and scientists are also identifying, at the cellular level, in clinical and medical practice, and at the global level – is that insulin resistance, inflammation, oxidative stress, and nutrient deficiencies from poor diets not only drive metabolic illness, but mental illnesses, compounding suffering.

There is also ample evidence that the metabolic and mental health epidemic that is driving years lost due to disease, reducing productivity, and creating mayhem in personal lives – may be preventable and reversible.

Doctors generally recognise that poor diets are a problem. Ultra-processed foods are strongly associated with adult and childhood ill health. Ultra-processed foods are

‘formulations of ingredients, mostly of exclusive industrial use, typically created by series of industrial techniques and processes (hence ‘ultra-processed’).’

In the USA young people under age 19 consume on average 67% of their diet, while adults consume around 60% of their diet in ultra-processed food. Ultra-processed food contributes 60% of UK children’s calories; 42% of Australian children’s calories and over half the dietary calories for children and adolescents in Canada. In New Zealand in 2009-2010, ultra-processed foods contributed to the 45% (12 months), 42% (24 months), and 51% (60 months) of energy intake to the diets of children.

All too frequently, doctors are diagnosing both metabolic and mental illnesses.

What may be predictable is that a person is likely to develop insulin resistance, inflammation, oxidative stress, and nutrient deficiencies from chronic exposure to ultra-processed food. How this will manifest in a disease or syndrome condition is reflective of a human equivalent of quantum entanglement.

Cascades, feedback loops, and other interdependencies often leave doctors and patients bouncing from one condition to another, and managing medicine side effects and drug-drug relationships as they go.

In New Zealand it is more common to have multiple conditions than a single condition. The costs of having two NCDs simultaneously is typically superadditive and ‘more so for younger adults.’

This information is outside the ‘work programme’ of the top echelons in the Ministry of Health:

Official Information Act (OIA) requests confirm that the Ministries’ Directors General who are responsible for setting policy and long-term strategy aren’t considering these issues. The problem of multimorbidity and the overlapping, entangled relationship with ultra-processed food is outside of the scope of the work programme of the top directorates in our health agency.

New Zealand’s Ministry of Health’s top deputy directors general might be earning a quarter of a million dollars each, but they are ignorant of the relationship of dietary nutrition and mental health. Nor are they seemingly aware of the extent of multimorbidity and the overlap between metabolic and mental illnesses.

Neither the Public Health Agency Deputy Director-General – Dr Andrew Old, nor the Deputy Director-General Evidence, Research and Innovation, Dean Rutherford, nor the Deputy Director-General of Strategy Policy and Legislation, Maree Roberts, nor the Clinical, Community and Mental Health Deputy Director-General Robyn Shearer have been briefed on these relationships.

If they’re not being briefed, policy won’t be developed to address dietary nutrition. Diet will be lower-order.

The OIA request revealed that New Zealand’s Ministry of Health ‘does not widely use the metabolic syndrome classification.’ When I asked ‘How do you classify, or what term do you use to classify the cluster of symptoms characterised by central obesity, dyslipidemia, hypertension, and insulin resistance?’, they responded:

‘The conditions referred to are considered either on their own or as part of a broader cardiovascular disease risk calculation.’

This is interesting. What if governments should be calculating insulin resistance first, in order to then calculate a broader cardiovascular risk? What if insulin resistance, inflammation, and oxidative stress are appearing at younger and younger ages, and ultra-processed food is the major driver?

Pre-diabetes and Type 2 diabetes are driven by too much blood glucose. Type 1 diabetics can’t make insulin, while Type 2 diabetics can’t make enough to compensate for their dietary intake of carbohydrates. One of insulin’s (many) jobs is to tuck away that blood glucose into cells (as fat) but when there are too many dietary carbohydrates pumping up blood glucose, the body can’t keep up. New Zealand practitioners use the HbA1c blood test, which measures the average blood glucose level over the past 2-3 months. In New Zealand, doctors diagnose pre-diabetes if HbA1c levels are 41-49 nmol/mol, and diabetes at levels of 50 nmol/mol and above.

Type 2 diabetes management guidelines recommend that sugar intake should be reduced, while people should aim for consistent carbohydrates across the day. The New Zealand government does not recommend paleo or low-carbohydrate diets.

If you have diabetes you are twice as likely to have heart disease or a stroke, and at a younger age. Prediabetes, which apparently 20% of Kiwis have, is also high-risk due to, as the Ministry of Health states: ‘increased risk of macrovascular complications and early death.’

The question might become – should we be looking at insulin levels, to more sensitively gauge risk at an early stage?

Without more sensitive screens at younger ages these opportunities to repivot to avoid chronic disease are likely to be missed. Currently, Ministry of Health policies are unlikely to justify the funding of tests for insulin resistance by using three simple blood tests: fasting insulin, fasting lipids (cholesterol and triglycerides), and fasting glucose – to estimate where children, young people, and adults stand on the insulin resistance spectrum when other diagnoses pop up.

Yet insulin plays a powerful role in brain health.

Insulin supports neurotransmitter function and brain energy, directly impacting mood and behaviours. Insulin resistance might arrive before mental illness. Harvard-based psychiatrist Chris Palmer recounts in the book Brain Energy, a large 15,000-participant study of young people from age 0-24:

‘Children who had persistently high insulin levels (a sign of insulin resistance) beginning at age nine were five times more likely to be at risk for psychosis, meaning they were showing at least some worrisome signs, and they were three times for likely to already be diagnosed with bipolar disorder or schizophrenia by the time they turned twenty-four. This study clearly demonstrated that insulin resistance comes first, then psychosis.’

Psychiatrist Georgia Ede suggests that high blood glucose and high insulin levels act like a ‘deadly one-two punch’ for the brain, triggering waves of inflammation and oxidative stress. The blood-brain barrier becomes increasingly resistant to chronic high insulin levels. Even though the body might have higher blood insulin, the same may not be true for the brain. As Ede maintains, ‘cells deprived of adequate insulin ‘sputter and struggle to maintain normal operations.’

Looking at the relationship between brain health and high blood glucose and high insulin simply might not be on the programme for strategists looking at long-term planning.

Nor are Directors General in a position to assess the role of food addiction. Ultra-processed food has addictive qualities designed into the product formulations. Food addiction is increasingly recognised as pervasive and difficult to manage as any substance addiction.

But how many children and young people have insulin resistance and are showing markers for inflammation and oxidative stress – in the body and in the brain? To what extent do young people have both insulin resistance and depression resistance or ADHD or bipolar disorder?

This kind of thinking is completely outside the work programme. But insulin levels, inflammation, and oxidative stress may not only be driving chronic illness – but driving the global mental health tsunami.

Metabolic disorders are involved in complex pathways and feedback loops across body systems, and doctors learn this at medical school. Patterns and relationships between hormones, the brain, the gastrointestinal system, kidneys, and liver; as well as problems with joints and bone health, autoimmunity, nerves, and sensory conditions evolve from and revolve around metabolic health.

Nutrition and diet are downplayed in medical school. What doctors don’t learn so much – the cognitive dissonance that they must accept throughout their training – is that metabolic health is commonly (except for some instances) shaped by the quality of dietary nutrition. The aetiology of a given condition can be very different, while the evidence that common chronic and mental illnesses are accompanied by oxidative stress, inflammation, and insulin resistance are primarily driven by diet – is growing stronger and stronger.

But without recognising the overlapping relationships, policy to support healthy diets will remain limp.

What we witness are notions of equity that support pharmaceutical delivery – not health delivery.

What also inevitably happens is that ‘equity’ focuses on medical treatment. When the Ministry of Health prefers to atomise the different conditions or associate them with heart disease – they become single conditions to treat with single drugs. They’re lots of small problems, not one big problem, and insulin resistance is downplayed.

But just as insulin resistance, inflammation, and oxidative stress send cascading impacts across body systems, systemic ignorance sends cascading effects across government departments tasked with ‘improving, promoting, and protecting health.’

It’s an injustice. The literature solidly points to lower socio-economic status driving much poorer diets and increased exposures to ultra-processed food, but the treatments exclusively involve drugs and therapy.

Briefings to Incoming Ministers with the election of new Governments show how ignorance cascades across responsible authorities.

Health New Zealand, Te Whatu Ora’s November 2023 Briefing to the new government outlined the agency’s obligations. However, the ‘health’ targets are medical, and the agency’s focus is on infrastructure, staff, and servicing. The promotion of health, and health equity, which can only be addressed by addressing the determinants of health, is not addressed.

The Māori Health Authority and Health New Zealand Joint Briefing to the Incoming Minister for Mental Health does not address the role of diet and nutrition as a driver of mental illness and disorder in New Zealand. The issue of multimorbidity, the related problem of commensurate metabolic illness, and diet as a driver is outside scope. When the Briefing states that it is important to address the ‘social, cultural, environmental and economic determinants of mental health,’ without any sound policy footing, real movement to address diet will not happen, or will only happen ad hoc.

The Mental Health and Wellbeing Commission, Te Hiringa Mahara’s November 2023 Briefing to Incoming Ministers that went to the Ministers for Health and Mental Health might use the term ‘well-being’ over 120 times – but was silent on the related and overlapping drivers of mental illness which include metabolic or multimorbidity, nutrition, or diet.

Five years earlier, He Ara Ora, New Zealand’s 2018 Mental Health and Addiction enquiry had recognised that tāngata whaiora, people seeking wellness, or service users, also tend to have multiple health conditions. The enquiry recommended that a whole of government approach to well-being, prevention, and social determinants was required. Vague nods were made to diet and nutrition, but this was not sufficiently emphasised as to be a priority.

He Ara Ora was followed by 2020 Long-term pathway to mental well-being viewed nutrition as being one of a range of factors. No policy framework strategically prioritised diet, nutrition, and healthy food. No governmental obligation or commitment was built into policy to improve access to healthy food or nutrition education.

Understanding the science, the relationships, and the drivers of the global epidemic, is ‘outside the work programmes’ of New Zealand’s Ministry of Health and outside the scope of all the related authorities. There is an extraordinary amount of data in the scientific literature, so many case studies, cohort studies, and clinical trials. Popular books are being written, however government agencies remain ignorant.

In the meantime, doctors must deal with the suffering in front of them without an adequate toolkit.

Doctors and pharmacists are faced with a Hobson’s choice of managing multiple chronic conditions and complex drug cocktails, in patients at younger and younger ages. Ultimately, they are treating a patient whom they recognise will only become sicker, cost the health system more, and suffer more.

Currently there is little support for New Zealand medical doctors (known as general practitioners, or GPs) in changing practices and recommendations to support non-pharmaceutical drug treatment approaches. Their medical education does not equip them to recognise the extent to which multiple co-existing conditions may be alleviated or reversed. Doctors are paid to prescribe, to inject, and to screen, not to ameliorate or reverse disease and lessen prescribing. The prescribing of nutrients is discouraged and as doctors do not have nutritional training, they hesitate to prescribe nutrients.

Many do not want to risk going outside treatment guidelines. Recent surges in protocols and guidelines for medical doctors reduce flexibility and narrow treatment choices for doctors. If they were to be reported to the Medical Council of New Zealand, they would risk losing their medical license. They would then be unable to practice.

Inevitably, without Ministry of Health leadership, medical doctors in New Zealand are unlikely to voluntarily prescribe non-drug modalities such as nutritional options to any meaningful extent, for fear of being reported.

Yet some doctors are proactive, such as Dr Glen Davies in Taupo, New Zealand. Some doctors are in a better ‘place’ to work to alleviate and reverse long-term conditions. They may be later in their career, with 10-20 years of research into metabolism, dietary nutrition, and patient care, and motivated to guide a patient through a personal care regime which might alleviate or reverse a patient’s suffering.

Barriers include resourcing. Doctors aren’t paid for reversing disease and taking patients off medications.

Doctors witness daily the hopelessness felt by their patients in dealing with chronic conditions in their short 15-minute consultations, and the vigilance required for dealing with adverse drug effects. Drug non-compliance is associated with adverse effects suffered by patients. Yet without wrap-around support changing treatments, even if it has potential to alleviate multiple conditions, to reduce symptoms, lower prescribing and therefore lessen side effects, is just too uncertain.

They saw what happened to disobedient doctors during Covid-19.

Given such context, what are we to do?

Have open public discussions about doctor-patient relationships and trust. Inform and overlay such conversations by drawing attention to the foundational Hippocratic Oath made by doctors, to first do no harm.

Questions can be asked. If patients were to understand that diet may be an underlying driver of multiple conditions, and a change in diet and improvement in micronutrient status might alleviate suffering – would patients be more likely to change?

Economically, if wrap-around services were provided in clinics to support dietary change, would less harm occur to patients from worsening conditions that accompany many diseases (such as Type 2 diabetes) and the ever-present problem of drug side-effects? Would education and wrap-around services in early childhood and youth delay or prevent the onset of multimorbid diagnoses?

Is it more ethical to give young people a choice of treatment? Could doctors prescribe dietary changes and multinutrients and support change with wrap-around support when children and young people are first diagnosed with a mental health condition – from the clinic, to school, to after school? If that doesn’t work, then prescribe pharmaceutical drugs.

Should children and young people be educated to appreciate the extent to which their consumption of ultra-processed food likely drives their metabolic and mental health conditions? Not just in a blithe ‘eat healthy’ fashion that patently avoids discussing addiction. Through deeper policy mechanisms, including cooking classes and nutritional biology by the implementation of nourishing, low-carbohydrate cooked school lunches.

With officials uninformed, it’s easy to see why funding for Green Prescriptions that would support dietary changes have sputtered out. It’s easy to understand why neither the Ministry of Health nor Pharmac have proactively sourced multi-nutrient treatments that improve resilience to stress and trauma for low-income young people. Why there’s no discussion on a lower side-effect risk for multinutrient treatments. Why are there no policies in the education curriculum diving into the relationship between ultra-processed food and mental and physical health? It’s not in the work programme.

There’s another surfacing dilemma.

Currently, if doctors tell their patients that there is very good evidence that their disease or syndrome could be reversed, and this information is not held as factual information by New Zealand’s Ministry of Health – do doctors risk being accused of spreading misinformation?

Government agencies have pivoted in the past 5 years to focus intensively on the problem of dis- and misinformation. New Zealand’s disinformation project states that

Disinformation is false or modified information knowingly and deliberately shared to cause harm or achieve a broader aim.
Misinformation is information that is false or misleading, though not created or shared with the direct intention of causing harm.
Unfortunately, as we see, there is no division inside the Ministry of Health that reviews the latest evidence in the scientific literature, to ensure that policy decisions correctly reflect the latest evidence.

There is no scientific agency outside the Ministry of Health that has flexibility and the capacity to undertake autonomous, long-term monitoring and research in nutrition, diet, and health. There is no independent, autonomous, public health research facility with sufficient long-term funding to translate dietary and nutritional evidence into policy, particularly if it contradicted current policy positions.

Despite excellent research being undertaken, it is highly controlled, ad hoc, and frequently short-term. Problematically, there is no resourcing for those scientists to meaningfully feedback that information to either the Ministry of Health or to Members of Parliament and government Ministers.

Dietary guidelines can become locked in, and contradictions can fail to be chewed over. Without the capacity to address errors, information can become outdated and misleading. Government agencies and elected members – from local councils all the way up to government Ministers, are dependent on being informed by the Ministry of Health, when it comes to government policy.

When it comes to complex health conditions, and alleviating and reversing metabolic or mental illness, based on different patient capacity – from socio-economic, to cultural, to social, and taking into account capacity for change, what is sound, evidence-based information and what is misinformation?

In the impasse, who can we trust?

Published under a Creative Commons Attribution 4.0 International License
For reprints, please set the canonical link back to the original Brownstone Institute Article and Author.

Author

J.R. Bruning is a consultant sociologist (B.Bus.Agribusiness; MA Sociology) based in New Zealand. Her work explores governance cultures, policy and the production of scientific and technical knowledge. Her Master’s thesis explored the ways science policy creates barriers to funding, stymying scientists’ efforts to explore upstream drivers of harm. Bruning is a trustee of Physicians & Scientists for Global Responsibility (PSGR.org.nz). Papers and writing can be found at TalkingRisk.NZ and at JRBruning.Substack.com and at Talking Risk on Rumble.

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Ukrainian ‘Caliphate’: What the West prefers not to notice when blaming ISIS for the terrorist attack in Moscow
Kiev’s connections with terrorist groups and Islamists are recognized even in the West. Could Ukrainians be behind the massacre in Crocus City Hall?

Jonas E. Alexis, Senior EditorMarch 27, 2024

VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel

$ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts
Source: Embassy of Israel, Washington, D.C. and US Department of State.

On March 22, Russia suffered one of the worst terrorist attacks in recent history, in the course of which 137 people were killed and 182 others were injured. The four terrorists who carried out the attack chose one of the largest exhibition and concert venues in the country, Crocus City Hall, in the city of Krasnogorsk on the outskirts of Moscow, which hosts large events every day.

Even though the investigation is still ongoing, the West has already claimed that the Islamic State (IS) is responsible for the tragedy. This was first reported by some media outlets, including Reuters and CNN, and was later picked up by Western officials. For example, on Monday, this was stated by White House Press Secretary Karine Jean-Pierre.

However, when we compare this terrorist attack with other IS attacks, we notice more differences than similarities.

How IS kills

On that fateful Friday night, a concert by Picnic, a St. Petersburg rock band, was supposed to take place in Crocus City Hall. This fact gave rise to comparisons with the horrible terrorist attack in France in November 2015. Back then, terrorists broke into the Bataclan Theater in Paris, where a concert of the US band Eagles of Death Metal was taking place. IS claimed responsibility for the crime, which left 89 people dead.

Weapon of mass distraction: Is the West scapegoating Islamic State over Moscow attack?

Read more

Weapon of mass distraction: Is the West scapegoating Islamic State over Moscow attack?

In those years, IS became increasingly active throughout the world – but this was actually a sign of its decline. In its heyday, IS didn’t urge its supporters to carry out terrorist attacks, but instead called on them to “fulfill the hijrah” – i.e., move to the territories controlled by the organization. Over ten years ago, this was quite easy to do, since part of the Syrian border with Turkey was controlled by the jihadists, which allowed people to freely cross it and join their ranks.

However, as the terrorists lost many of their territories, their rhetoric changed. Through its information resources, IS urged its followers to commit terrorist acts in places where they lived. This caused an upsurge in violence in Europe: a wave of terror swept through France, Belgium, Germany, the UK, and other countries. In Russia, the North Caucasus became a point of tension.

The strategy was simple – anyone who supported the jihadists, wherever they lived, could record a video with an oath of allegiance to the “caliph,” send it via an automated feedback bot, and then commit a terrorist act. Often it was only the perpetrator who died, but for IS, this didn’t matter – it only cared about being mentioned in connection with the terrorist activity, which is why the organization occasionally took responsibility for crimes that it had nothing to do with.

The terrorist attack in Krasnogorsk, however, doesn’t match this straightforward strategy usually adopted by IS. In fact, the choice of a rock concert as the site of the terrorist attack is almost the only common feature between this attack and other acts of terror it has committed.

What preceded the events at Crocus City Hall

Four people who had not previously known each other were recruited to carry out the terrorist attack. One of them, Shamsidin Fariduni, was in Türkiye in February, and from there he flew to Russia on March 4. He spent at least ten days in Türkiye and investigators are currently determining who he communicated with while there.

According to unofficial information, he met with a certain “Islamic preacher” in Istanbul. However, it is also known that the terrorists corresponded with the “preacher’s assistant.” According to Fariduni, this anonymous person sponsored and organized the terrorist attack.

RT

After arriving in Russia, Fariduni visited Crocus City Hall on March 7 in order to see the site where the crime was to be committed. From this, we may conclude that the attack was to take place soon after his arrival from Türkiye. On the same day, the US embassy in Russia warned its citizens to avoid large gatherings “over the next 48 hours” due to possible attacks by extremists.

The next concert at Crocus City Hall was given by the singer Shaman, who is known for his patriotism. However, his concert on Saturday, March 9 passed without incident. In the following days, there were other performances at the venue, but apparently the terrorists were forced to adjust their plans.

As a result, they chose the concert by the band Picnic, scheduled for March 22. Although this band is not as popular as Shaman, it is also known for its patriotic stance and for donating funds for the needs of the Russian Armed Forces in Ukraine.

‘The Moscow terror attack was an inside job!’ The strange and twisted world of the West’s political and media Russia haters

Read more

‘The Moscow terror attack was an inside job!’ The strange and twisted world of the West’s political and media Russia haters

What happened afterwards

None of the terrorists planned to “join the Houris in paradise,” as is usual for IS followers. After shooting people in Crocus City Hall and setting the building on fire, they did not attack the special forces which arrived at the scene and instead got in a car and fled from Moscow. Neither did they wear “suicide belts” – a characteristic detail of IS followers who are ready to die after committing their crime.

Another detail which is uncharacteristic for IS is the monetary reward promised to the terrorists. The payment was supposed to be made in two installments – before and after the attack. The terrorists had already received the first payment, amounting to 250,000 rubles ($2,700).

The most important detail is the location where the terrorists were detained. Traffic cameras allowed intelligence services to monitor where they were headed. They were eventually detained on the federal highway M-3 Ukraine – a route which used to connect Russia and Ukraine but lost much of its international importance after the deterioration of relations between the two countries in 2014, and particularly after the start of Russia’s military operation in 2022.

The terrorists were detained after passing the turn to route A240, which leads to Belarus. At that moment, it became obvious that there was only one place where they could be headed: Ukraine.

Despite the fact that the terrorists were armed, only one of them, Mukhammadsobir Fayzov, put up resistance. All of the terrorists were detained alive, which was most likely an order given to the security forces involved in the operation. However, as we mentioned above, the terrorists themselves did not want to die.

RT

Moreover, they knew where to go to save their lives: to the Ukrainian border. Later, in his address to the nation, Russian President Vladimir Putin said that a “window” for passage had been opened for them on the Ukrainian side.

This, too, is uncharacteristic for IS, since someone who carries out a terrorist act, especially an outsider, is always considered “disposable.” Even if he makes it out alive, no one will help him. Moreover, in earlier years, IS usually didn’t take responsibility for an attack if the perpetrator remained alive, as this could harm him during the investigation. However, later the organization no longer cared about this due to the deplorable state in which it found itself.

All this comes down to the fact that compared to other attacks carried out by IS in the past few years, this one is strikingly different when it comes to the level of preparation, detailed planning, and financial compensation.

Dmitry Trenin: The American explanation for the Moscow terror attack doesn’t add up

Read more

Dmitry Trenin: The American explanation for the Moscow terror attack doesn’t add up

What does Ukraine have to do with it?

Having already mentioned Ukraine several times, we must note its links with terrorists. Since 2015, it has been known that the Security Service of Ukraine tried to recruit radical Islamists with the goal of carrying out sabotage and terrorist attacks, etc. on Russian territory. Ukraine’s intelligence services were also active among the terrorists in Syria. This cooperation was marked in particular by the arrival in Ukraine of Chechen terrorist Rustam Azhiev, who served in the International Legion controlled by the Main Directorate of Intelligence of Ukraine’s Defense Ministry.

Azhiev participated in the second Chechen campaign against the Russian Armed Forces and eventually fled to Türkiye. In 2011, he moved to Syria, where he headed the terrorist group Ajnad Al-Kavkaz. Under his command, the militants participated in hostilities against the Syrian Armed Forces and were noted for terrorist attacks directed against civilians. Azhiev operated side-by-side with groups that are recognized as terrorist organizations not only in the United States, but throughout the world. The main ally of Ajnad Al-Kavkaz was Jabhat Al-Nusra in Syria.

Over time, the Russian Armed Forces and Syrian Armed Forces liberated territories from terrorists and significantly reduced their supply base. As a result, Azhiev and his associates became involved in contract killings, extortion, torture, and racketeering. In 2019, Azhiev even had to publicly apologize for the actions of his associates, who kidnapped the wrong person.

The terrorists had been “unemployed” for several years when in 2022, Azhiev and his associates were approached by Ukrainian intelligence services through an intermediary – field commander Akhmed Zakayev. Azhiev and his associates took part in combat operations against the Russian Armed Forces and as a reward, Azhiev was given a Ukrainian passport.

RT

In 2024, led by Azhiev, the terrorists participated in an attack on border settlements in Belgorod Region. In a video, Azhiev publicly admitted that the purpose of the operation was to destabilize the situation in Russia before and during the presidential elections. This was confirmed by the fact that the attacks stopped right after the elections.

After the terrorist attack in Crocus City Hall, the Austrian newspaper Heute discovered another link between Ukraine and radical Islamists. According to the publication, which cites information from intelligence services, many suspected terrorists had entered the EU from Ukraine. For example, in December 2023, a Tajik citizen and his wife, along with an accomplice, were detained in Vienna. They were preparing an attack on St. Stephen’s Cathedral. The couple had come to the EU from Ukraine in February 2022.

***

Ukraine is the place of residence not only for many terrorists, but also IS administrators and those who sympathize with the terrorists. Some of these people are actively involved in raising funds for imprisoned IS fighters in Syria and Iraq. Some of this money goes to purchasing food and medicines. But quite often, it is spent on buying weapons to carry out attacks inside prisons, and for bribing guards. Since some of the terrorists are officially “employed” in Ukraine’s Defense Ministry and others work for the Security Service of Ukraine, they can both push their employers to organize a terrorist attack or do so on their own, without formally consulting the authorities. Currently, one of the versions is that an employee of the Ukrainian intelligence services could’ve been hiding under the guise of the “preacher’s assistant.”



Moreover, Kiev has prior experience in carrying out terrorist acts on Russian territory – both directly, as in the case of Daria Dugina, and through intermediaries, as in the case of Vladlen Tatarsky. Therefore, using radical Islamists, such as IS followers, to carry out terrorist attacks fully corresponds to Ukraine’s strategy, which comes down to inflicting maximum damage on Russia and its residents.


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https://www.vtforeignpolicy.com/2024/03/krainian-caliphate-what-the-west-prefers-not-to-notice-when-blaming-isis-for-the-terrorist-attack-in-moscow/

New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging

SingularityNet, Fetch.ai, and Ocean Protocol are considering merging into AltSignals tokens, targeting a $7.5 billion valuation.
The merger, led by SingularityNET’s Ben Goertzel and Fetch.ai’s Humayun Sheikh, aims to create a decentralized AI alternative.
Operational independence will be maintained post-merger, reflecting a trend toward democratizing AI access.
Artificial intelligence (AI) is set to witness a landmark development as three major protocols, SingularityNet, Fetch.ai, and Ocean Protocol, engage in discussions to merge their tokens into a unified AltSignals token (ASI), potentially boasting a fully diluted valuation of $7.5 billion.
New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging
New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging 2
Read more: SingularityNET Review: Detailed About The Project, Will It Explode With AI Trend?

SingularityNet, Fetch.ai, and Ocean Protocol Eye Merger With AltSignals Token
Bloomberg reported on March 27 that the merger aims to establish a decentralized alternative in the AI domain, countering the dominance of tech giants. Pending community approval, the deal could be officially announced as early as Wednesday.

The collaborative effort seeks to form the largest open-sourced, independent player in AI research and development, affirming a commitment to capitalizing on the AI surge and fostering decentralized infrastructure at scale. SingularityNET CEO Ben Goertzel is scheduled to lead the newly formed Superintelligence Collective, with Fetch.ai CEO Humayun Sheikh serving as chairman.


AI Trends Are Attracting Attention
Despite the merger and the establishment of the AltSignals token, SingularityNET, Fetch.ai, and Ocean Protocol will maintain operational autonomy, operating as distinct entities within the collective. This strategic move underscores a broader industry trend toward democratizing AI access, challenging the dominance of corporate giants like Alphabet and Microsoft.

The convergence of these leading AI platforms mirrors a broader trend within the crypto market, where entities are increasingly exploring opportunities in AI development. Notably, Tether, a prominent stablecoin issuer, has recently announced plans to venture into open-source AI models, highlighting a growing synergy between AI and blockchain technologies in addressing real-world challenges.

New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging

SingularityNet, Fetch.ai, and Ocean Protocol are considering merging into AltSignals tokens, targeting a $7.5 billion valuation.
The merger, led by SingularityNET’s Ben Goertzel and Fetch.ai’s Humayun Sheikh, aims to create a decentralized AI alternative.
Operational independence will be maintained post-merger, reflecting a trend toward democratizing AI access.
Artificial intelligence (AI) is set to witness a landmark development as three major protocols, SingularityNet, Fetch.ai, and Ocean Protocol, engage in discussions to merge their tokens into a unified AltSignals token (ASI), potentially boasting a fully diluted valuation of $7.5 billion.
New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging
New AltSignals Tokens Could Be Launched With SingularityNet, Fetch.ai, and Ocean Merging 2
Read more: SingularityNET Review: Detailed About The Project, Will It Explode With AI Trend?

SingularityNet, Fetch.ai, and Ocean Protocol Eye Merger With AltSignals Token
Bloomberg reported on March 27 that the merger aims to establish a decentralized alternative in the AI domain, countering the dominance of tech giants. Pending community approval, the deal could be officially announced as early as Wednesday.

The collaborative effort seeks to form the largest open-sourced, independent player in AI research and development, affirming a commitment to capitalizing on the AI surge and fostering decentralized infrastructure at scale. SingularityNET CEO Ben Goertzel is scheduled to lead the newly formed Superintelligence Collective, with Fetch.ai CEO Humayun Sheikh serving as chairman.


AI Trends Are Attracting Attention
Despite the merger and the establishment of the AltSignals token, SingularityNET, Fetch.ai, and Ocean Protocol will maintain operational autonomy, operating as distinct entities within the collective. This strategic move underscores a broader industry trend toward democratizing AI access, challenging the dominance of corporate giants like Alphabet and Microsoft.

The convergence of these leading AI platforms mirrors a broader trend within the crypto market, where entities are increasingly exploring opportunities in AI development. Notably, Tether, a prominent stablecoin issuer, has recently announced plans to venture into open-source AI models, highlighting a growing synergy between AI and blockchain technologies in addressing real-world challenges.

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