• 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"....






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

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

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    And with that said

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    I'd like to first tell you the story about

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    this uh... little girl named Dana

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

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

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    uh... she had when we were in Boston

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

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    and uh...

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    I rembember her being admitted and she was excited at first

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    and then just before they got into her the OR

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

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    who wouldn't be? Because surgeries today are complicated

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    and they're often very risky.

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

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    Dana will arrive to hospital for her ??? surgery

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    and instead of being prepped for anesthesia for the OR

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    the surgeon will just take a syringe and inside the syringe

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    there are millions of tiny robots, of tiny machines

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    that will be injected into Dana's bloodstream.

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

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    they will excite out the injured tissue,

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    then will remove dead cells,

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    then they will...

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

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    they will release drugs that relief pain and reduce inflammation

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    and all the while Dana will be sitting on the chair

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

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

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    And...(giggles)

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    uh... when these robots

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    have completed their job they'll simply disintegrate

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    and disappear from her bloodstream the next day.

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    So these nanobots have been envisioned in the past 30 years

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

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

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    here in Israel.

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    I'll show you this syringe

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    which I've brought from my lab.

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    So this syringe has inside it a thousand billion robots.

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    So these robots are each fifty nanometers

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

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

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

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

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    But over the past year and a half

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    in my group at Bar-Ilan University

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

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    medical and therapeutic tasks.

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    We've invented ways of making them safe for use

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    and non-inmunogenic

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    and we learned how to tune their stability in our bloodstream

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    to fit either short-term or long-term

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    even days long medical procedures.

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    So to carry out medical and therapeutic procedures in our body

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    with the upmost precision,

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    we need to be able to control molecules

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    Controlling molecules is a very simple challenge

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    in modern scientific knowledge.

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

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    So despite...

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    amazing progress made in the past four decades

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

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    has been essentially unchanged

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    and it's similar as two hundred years ago

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    right? You hear about about big pharmaceutical companies

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    spending huge amounts of money

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    searching for better, safer drugs.

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    Attempts that usually fail.

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    OK? but,

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    searching for let's say a safer cancer drug,

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

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    Because searching for a safer cancer drug

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

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    We don't search for such guns,

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    what we do is training soldiers to use that gun properly

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

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    But there are things we can do with drugs

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    for example, we can put the drugs

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    in particles from which they difuse slowly.

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    We can attach a drug to a carrier

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    which takes someplace but, this is not real control.

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    When we were thinking about control we're thinking about

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    processes is the real world around us

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    and what happens when we want to control a process

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    that's beyond our capabilities as humans

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    we just connect this process to a computer

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    and let the computer control this process for us.

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    OK? So that's what we do.

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    But obviously this cannot be done with drugs because

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

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    The computer is in fact so much bigger

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

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    Our nanobots which were in the syringe

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    solve this problem because they are in fact

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    computers the size of molecules.

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    and they can interact with molecules

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    and they can control molecules directly,

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    so just think about all those

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    drugs that have been withdrawn from the market

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    for excessive toxicity

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    right?

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    It doesn't mean that they are not effective,

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    they were amazingly effective,

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    they were just guns shooting in all directions

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    but in the hands of a well-trained soldier

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    or a well-programed nanobot

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    using all the existing drugs

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    we could hypothetically kill almost any disease.

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    So we might not need even new drugs.

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    We have amazing drugs already,

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

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    and our nanobots...

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

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    So there is an interesting question "how do we build

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

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    so the simple answer would be: we can use molecules

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    to build this machine.

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

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

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    which is DNA.

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    And in fact every part of the robot,

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    every part of out nanorobots:

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    Moving parts, axis, locks, chasis, software,

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    everything is made from DNA molecules.

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    And the techonology that enables us to do this

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

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

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    which was also featured in TED,

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    and it's called DNA origami.

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

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    we use a single long strand of DNA

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    and we fold it into virtually any shape we want.

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    For example these shapes, so these are actual microscopic images

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

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

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    are a hundred nanometers in size

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

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    Now since 2006 several researchers, really talented ones,

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

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

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    using this technique.

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    And these researchers also gave us computer-aided design tools

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    that enable everyone

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    very very simply to design objects from DNA

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    So these CAD tools amazingly

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    enable us to focus o n the shape we want

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

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

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

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    is a spreadsheet with fragments of DNA

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

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

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    several days later to your doorstep

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

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    and these molecular bricks will self-assemble into

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

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

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

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

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

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

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

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

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    and the nanobot can be programmed to turn on and off

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    these functions at certain places and at certain times

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    this is how we control those molecules

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

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    sequestres anything, any payload you put inside

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

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    for example, it cannot engage target cells or target tissues

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

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    based on molecular cues it finds from the environment

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    so programming the robot is virtually like assemblying a combination lock

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    using disks that recognize digits,

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

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

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    any cargo inside is now accessible,

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    it can attack target cells or target tissues

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    or other robots which you'll see later on.

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

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

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    We can control which payload becomes accessible at which time point

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

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    So what you can do is you can take nanobots,

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    you can put the nastiest cancer drug you may find

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    into the robots, even a cancer drug

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    that's been withdrawn because of excessive toxicity

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    Ok? When the robot is locked

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

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    nothing happens, no cell is affected, because the robot

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    safely sequesters those drugs inside.

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    When we unlock the robots

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

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

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    to help us see better the output.

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

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    so only the tumor cells

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    uh... only the tumor cells die because

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

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    So it does not harm them at all.

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    And we have nanorobots in our lab that can target

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    about ten types of cancer already and other cell targets

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    and my team keeps expanding this range monthly.

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    So these are nanorobots and to another topic

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    organisms in nature, like bacteria and animals

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

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    conveys advantage

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    and capabilities beyond those of the individual

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    and since we are interested in

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    very complex medical procedures, very complex therapeutic settings,

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    we're wondering what we could do

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    if we could engineer artificial swarm behaviors

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

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    Can we teach them to behave like animals, like insects

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

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    So you could think one way to do it would be

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    to look at a natural swarm like this one of fish

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

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    in molecules of course

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    that mimic the same behaviour

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    this is virtually impossible, it's impractical

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

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    and you design a very basic set of interaction rules

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

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    and you let the behaviours emerge from that group

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

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    for example, just as ants

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    can shake hands and form physical bridges between two trees

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    or two remote parts of the same tree,

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    we already have nanorobots that can reach out for each other

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    touch each other and shake hands in such a way

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    they form physical bridges.

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    Then you can imagine these robots

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    extending, making bridges extending from one-half

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    to the other half of an injured tissue,

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    an injured spinal cord for example

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

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    and once they stretched over that tissue gap

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

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

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    So we already did that and...

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

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    and this is amazing because as you can see here

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

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

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    while "B" is not and viceversa.

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    So this is good for combination therapy

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    with combination therapy we take multiple drugs, right?

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    and sometimes two or more of these drugs

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    can collide and generate side effects,

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

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    and the robots will time the activities so that

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

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

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    Another example that we did is the quorum sensing.

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

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    It means nanorobots can count themselves

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

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    this is a mechanism invented by bacteria in evolution

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    and they regulate amazing behaviours based on just their population density

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

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    so our robots can count themselves and switch to on

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

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

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    to become active only when reaching a certain dose

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

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

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    so this nanobots can do computing.

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

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

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

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

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    and these logic gates are set to interact to produce computations

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    so we can also produce computation by setting interactions between nanorobots

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    to emulate logic gates like you see here

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    and they form chains and they form pairs

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

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    of computing based on interacting nanorobots

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    and to prototype these

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    we are using animals, very interesting animals

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    these are cockroaches,

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

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    they're actually from South America

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

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    [Laughter]

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

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

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    have you ever tried putting cockroach to sleep?

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    We put in the freezer for seven minutes

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    in they fall asleep

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    and we can inject these nanorobots inside

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

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    And those robots

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    while they're doing this, the robots read molecules

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    from the cockroaches' inputs

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    and they write their outputs in the form of drugs

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    activated on those cockroaches' cells

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

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    architectures of interecting nanorobots that can emulate logical operators

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

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    [....]

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    that can control multiple drugs simultaneously

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

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

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    of an 8-bit computer like Commodore 64.

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

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    my team [has] developed nanorobots that carry antennae

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    these antennae are made from metal nano-particles.

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    Now, the antennae enable the nanobots

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    to respond to externally applied electromagnetic fields

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    so these nanorobots, this version of nanobots

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

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    or for example using a controller

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

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

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    to control nanobots.

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    For example you can imagine nanorobots being injected

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    to Dana, my daughter for example,

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    and the doctor can guide those robots

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

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    And you can already see an example where we actually took

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    cancer cells and loaded robots with cancer drugs

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    and activated the drug by a hand gesture.

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

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    as you can see here.

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    And the interesting thing is that

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

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    the controller actually links those nanobots to the network

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    so they have an actual IP address

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

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    for example, my doctor's smartphone

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

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

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

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    has their own unique molecular signature

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

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    and if you know these molecules

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

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    and you can program them to look for bits,

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    this could be for example signally molecules between cells,

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    and either fetch them for diagnostics

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    or carry them to different addresses.

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    And we already have robots that can hijack

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    signals between cells

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    and manipulate an entire network of communications between cells

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

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    communicate and orchestrate to perpetuate a disease.

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    So before I finish I'd just like to thank

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    my amazing team at Bar-Ilan University

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

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    starting from the George Chuch's Lab in Harvard

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

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    and I really hope that

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    anywhere between a year and five years from now

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    we'll be able to use this in humans

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    and finally witness the emergence of nanobot society.

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    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
    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 Follow @zeeemedia Website | X | Instagram | Rumble https://donshafi911.blogspot.com/2024/04/the-emergence-of-nanobot-society.html
    OUTRAGED.SUBSTACK.COM
    The emergence of nanobot society
    So, they injected it into the military, police, emergency services.... Now everyone is injected with a device with a "real IP ADDRESS".... Thanks for reading OUTRAGED’s Newsletter! Subscribe for free to receive new posts and support my work. 0:00 Thank you very much. So one word of notice before we begin,
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  • The Shedding Disease
    What's going on and what to do about it

    Dr. Syed Haider

    Back in the 1300s during the Black Death plague outbreak in Europe, people were dropping like flies from this mystery illness. No one knew how it spread or how to protect themselves.

    Imagine their shock when some folks started getting sick without ever coming into direct contact with a plague victim!

    Turns out, the plague was spreading through fleas hitching a ride on rats. Even if you never touched a sick person, a plague-carrying flea could jump off a rat and bite you, infecting you with the deadly disease.

    Image
    Huge rat > truly gigantic flea > normal or tiny (?) peasant
    Crazy, right?

    Fast forward to today, and as most of you already know we might be facing a somewhat similar situation with the clot shots.

    For the FOBs (Fresh off the Boat from normie land), hear me out…

    So there's been a ton of stories popping up lately about unvaxxed people, mostly women, having all sorts of weird health issues after being around recently vaccinated folks.

    We're talking things like wacky periods, miscarriages, crazy autoimmune flares, cancers, strokes, etc, all in people who never got the jab themselves.

    At first it seemed like coincidence, but the reports kept piling up.

    It got many doctors scratching their heads (others like me didn’t scratch, we just knew) and wondering, could there be something to this?

    Image
    Man scratches head, Not me.
    Could vaccinated people be "shedding" something that's making unvaccinated people sick?

    There's a few theories flying around.

    One is that the spike proteins made by the vaccines are hitching a ride in tiny bubbles called exosomes that are released in breath, sweat, and other bodily fluids. So an unvaxxed person breathes in these exosomes and boom(!), the toxic spike proteins get into their body and start wreaking havoc. Some people seem super sensitive and react to even tiny amounts.

    Image
    Exosomes are just little bits of our cells membranes that bud off, and can carry anything inside them. In a way viruses are just a class of exosomes, but carrying genetic material that originated outside us (and then multiplied inside us).
    Another idea is that the vaccines are turning people into stealthy virus super-spreaders without them even knowing it. They might feel fine, but they could be carrying and shedding high amounts of virus to everyone around them. So it's not really something in the shot that's being shed, its that they catch COVID, have no symptoms and then just go around spreading COVID everywhere and it’s the COVID that causes the problem (sounds like Big Pharma cope to me, kind of like: it's all in their heads! So yeah, I’m not buying it either).

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

    Share

    There's even studies showing the vaccines contain DNA junk from the manufacturing process that might be messing with our microbiome and turning vaxxed people into walking bio-hazards (this is more like it).

    Some theories are farther out there, like it’s some kind of energetic imbalance, or it’s graphene oxide, or even some kind of nanotech (all your cells are belong to us! not very convincing imo).

    Image
    This is not real! My take on the "flashing lights" in the nanotech videos: spinning particulate crystals dispersing incident light from the microscope? The apparently self-assembling structures: chemical gardens? The broadcasted MAC addresses? Put that sample in a Faraday cage and check it again.
    Anyway, regardless of the mechanism there’s something strange going on.

    The science is still new (there's not much of a career in studying this stuff), but evidence is beginning to stack up suggesting that this "vaccine shedding" stuff might be legit.

    Researchers are finding vaccine cooties like mRNA, spike proteins, and weird DNA bits in saliva, vaginal secretions, sperm, breast milk, even the air around vaxxed people.

    Image
    For the love of God don’t vax the kiddos.
    So what to do?

    Figure out your personal risk level. Some folks seem to be more sensitive than others, especially if you already have health issues (or had spike toxicity before). Might be smart to take extra precautions.

    Rain check: avoid swapping saliva or other Fun Time Activities with vaxxed people if you can, at least for a few weeks to months after they get the shot.

    Feed your body the good stuff to beef up your natural defenses. We're talking clean eats, plenty of Zzz's, and immune-boosting supps like the sunshine vitamin (I mean actual sunshine), as well as actual supplements like C, D, zinc, and quercetin.

    Consider adding some anti-shedding supplements to your arsenal, like

    DETOX [spike buster] to bust up clots or ivermectin to nuke those spike proteins. Work with a dialed in doc (i.e. me) to find the right combo for you.

    If you got mega-dosed with someone's shed, you might need to pull out the big detox guns like plasma donation (which is better tho the paid, or more expensive, less available therapeutic plasmapheresis), ozone therapy, ultraviolet blood irradiation, low-dose naltrexone, microbiome restoration (i.e. stool transplants, probably somewhere in South America or maybe Australia), or IV exosomes. We can help with a custom detox plan at mygotodoc.com (that's me).

    Don't forget to clean your space! Some have reported you can detoxify a room where shedding occurred using hypochlorous acid (Danolyte) or Chlorine Dioxide. UV light systems may also be able to zap any shed cooties floating around (plus they kills normal COVID too, bonus!)

    Share

    Bottom line, we need way more research on this shedding stuff ASAP. But until we know for sure it's not a thing, better safe than shedding or shed upon.

    We all have the right to choose what goes in our bodies, and that includes not getting stealth dosed with someone else's vaccine gunk.

    The health bigwigs need to step up and take this seriously stat (yea right - someone needs to take them to the woodshed, or just shed on them).


    Until then (forever?), keep your eyes open, trust your gut, and do what you gotta do to stay safe out there!

    And if you think you got shed upon, speak up and find a doc who will actually listen (again: moi).

    Shedding is no joke, but together we'll get through this and come out stronger on the other side.

    Drop a comment below and let me know if you’ve been shed upon, what you know works and what else we should do (Nuremberg 2.0, anyone?).

    https://blog.mygotodoc.com/p/the-shedding-disease

    https://telegra.ph/The-Shedding-Disease-03-20
    The Shedding Disease What's going on and what to do about it Dr. Syed Haider Back in the 1300s during the Black Death plague outbreak in Europe, people were dropping like flies from this mystery illness. No one knew how it spread or how to protect themselves. Imagine their shock when some folks started getting sick without ever coming into direct contact with a plague victim! Turns out, the plague was spreading through fleas hitching a ride on rats. Even if you never touched a sick person, a plague-carrying flea could jump off a rat and bite you, infecting you with the deadly disease. Image Huge rat > truly gigantic flea > normal or tiny (?) peasant Crazy, right? Fast forward to today, and as most of you already know we might be facing a somewhat similar situation with the clot shots. For the FOBs (Fresh off the Boat from normie land), hear me out… So there's been a ton of stories popping up lately about unvaxxed people, mostly women, having all sorts of weird health issues after being around recently vaccinated folks. We're talking things like wacky periods, miscarriages, crazy autoimmune flares, cancers, strokes, etc, all in people who never got the jab themselves. At first it seemed like coincidence, but the reports kept piling up. It got many doctors scratching their heads (others like me didn’t scratch, we just knew) and wondering, could there be something to this? Image Man scratches head, Not me. Could vaccinated people be "shedding" something that's making unvaccinated people sick? There's a few theories flying around. One is that the spike proteins made by the vaccines are hitching a ride in tiny bubbles called exosomes that are released in breath, sweat, and other bodily fluids. So an unvaxxed person breathes in these exosomes and boom(!), the toxic spike proteins get into their body and start wreaking havoc. Some people seem super sensitive and react to even tiny amounts. Image Exosomes are just little bits of our cells membranes that bud off, and can carry anything inside them. In a way viruses are just a class of exosomes, but carrying genetic material that originated outside us (and then multiplied inside us). Another idea is that the vaccines are turning people into stealthy virus super-spreaders without them even knowing it. They might feel fine, but they could be carrying and shedding high amounts of virus to everyone around them. So it's not really something in the shot that's being shed, its that they catch COVID, have no symptoms and then just go around spreading COVID everywhere and it’s the COVID that causes the problem (sounds like Big Pharma cope to me, kind of like: it's all in their heads! So yeah, I’m not buying it either). Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share There's even studies showing the vaccines contain DNA junk from the manufacturing process that might be messing with our microbiome and turning vaxxed people into walking bio-hazards (this is more like it). Some theories are farther out there, like it’s some kind of energetic imbalance, or it’s graphene oxide, or even some kind of nanotech (all your cells are belong to us! not very convincing imo). Image This is not real! My take on the "flashing lights" in the nanotech videos: spinning particulate crystals dispersing incident light from the microscope? The apparently self-assembling structures: chemical gardens? The broadcasted MAC addresses? Put that sample in a Faraday cage and check it again. Anyway, regardless of the mechanism there’s something strange going on. The science is still new (there's not much of a career in studying this stuff), but evidence is beginning to stack up suggesting that this "vaccine shedding" stuff might be legit. Researchers are finding vaccine cooties like mRNA, spike proteins, and weird DNA bits in saliva, vaginal secretions, sperm, breast milk, even the air around vaxxed people. Image For the love of God don’t vax the kiddos. So what to do? Figure out your personal risk level. Some folks seem to be more sensitive than others, especially if you already have health issues (or had spike toxicity before). Might be smart to take extra precautions. Rain check: avoid swapping saliva or other Fun Time Activities with vaxxed people if you can, at least for a few weeks to months after they get the shot. Feed your body the good stuff to beef up your natural defenses. We're talking clean eats, plenty of Zzz's, and immune-boosting supps like the sunshine vitamin (I mean actual sunshine), as well as actual supplements like C, D, zinc, and quercetin. Consider adding some anti-shedding supplements to your arsenal, like DETOX [spike buster] to bust up clots or ivermectin to nuke those spike proteins. Work with a dialed in doc (i.e. me) to find the right combo for you. If you got mega-dosed with someone's shed, you might need to pull out the big detox guns like plasma donation (which is better tho the paid, or more expensive, less available therapeutic plasmapheresis), ozone therapy, ultraviolet blood irradiation, low-dose naltrexone, microbiome restoration (i.e. stool transplants, probably somewhere in South America or maybe Australia), or IV exosomes. We can help with a custom detox plan at mygotodoc.com (that's me). Don't forget to clean your space! Some have reported you can detoxify a room where shedding occurred using hypochlorous acid (Danolyte) or Chlorine Dioxide. UV light systems may also be able to zap any shed cooties floating around (plus they kills normal COVID too, bonus!) Share Bottom line, we need way more research on this shedding stuff ASAP. But until we know for sure it's not a thing, better safe than shedding or shed upon. We all have the right to choose what goes in our bodies, and that includes not getting stealth dosed with someone else's vaccine gunk. The health bigwigs need to step up and take this seriously stat (yea right - someone needs to take them to the woodshed, or just shed on them). Until then (forever?), keep your eyes open, trust your gut, and do what you gotta do to stay safe out there! And if you think you got shed upon, speak up and find a doc who will actually listen (again: moi). Shedding is no joke, but together we'll get through this and come out stronger on the other side. Drop a comment below and let me know if you’ve been shed upon, what you know works and what else we should do (Nuremberg 2.0, anyone?). https://blog.mygotodoc.com/p/the-shedding-disease https://telegra.ph/The-Shedding-Disease-03-20
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    The Shedding Disease
    What's going on and what to do about it
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  • 🚨Dr Lee Merritt : “Doctors around the world are showing that cancer is intracellular parasites”😳
    “If you look at cancer under a light microscope, its essentially indistinguishable from parasite egg sacs”

    Is that why they tried so hard to shut down Ivermectin and other anti-parasitics during #Covid?

    Should we be looking at cancer in a different way? Is cancer related to parasites, worms or fungus?

    https://rumble.com/v47y06r-dr-lee-merritt-doctors-around-the-world-are-showing-that-cancer-is-intracel.html
    🚨Dr Lee Merritt : “Doctors around the world are showing that cancer is intracellular parasites”😳 “If you look at cancer under a light microscope, its essentially indistinguishable from parasite egg sacs” Is that why they tried so hard to shut down Ivermectin and other anti-parasitics during #Covid? Should we be looking at cancer in a different way? Is cancer related to parasites, worms or fungus? https://rumble.com/v47y06r-dr-lee-merritt-doctors-around-the-world-are-showing-that-cancer-is-intracel.html
    Like
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  • Do You Know What’s in a Vaccine? Chemical Ingredients
    Addendum to the Childhood Vaccination Series


    All Global Research articles can be read in 51 languages by activating the Translate Website button below the author’s name.

    To receive Global Research’s Daily Newsletter (selected articles), click here.

    Click the share button above to email/forward this article to your friends and colleagues. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles.

    ***

    Over the last few decades, the number of chemicals added to foods and other products has skyrocketed. Chemicals are added to “enhance flavor”, make fruits and vegetables look fresh, extend the shelf life of packaged foods and for other invented reasons. A cornucopia of chemicals are also found in lotions and beauty products with the ostensible reason that these chemicals make beauty products feel, look, and smell nice.

    Along with this increase in heavily processed foods has come increased skepticism about the necessity of inserting chemical additives into everything we touch and taste. A significant and growing segment of the US population are beginning to examine the health consequences of ingesting and absorbing these chemical-laden products.

    This growing awareness about the adverse effects of ingesting and absorbing synthetic ingredients and the public’s understanding of the attendant health benefits of consuming products free from synthetic chemicals has prompted consumers to seek out organic ingredient-based items in their foods and skin lotions.

    More people are showing interest in knowing about the ingredients in their food and striving to ‘eat clean.’ This increased awareness is evidenced in the steady growth of the organic food industry and trends in the natural and organic cosmetic industry where demand is higher than ever.

    This same level of concern has begun to seep into the public conscience regarding a certain medical product that has mostly avoided scrutiny – the vaccine.

    Having been trained to accept that this product is a customary aspect of everyday life, most people haven’t given much thought to what’s inside the vaccine vials. Rarely will the vaccine ritual in the doctor’s office include a discussion about the ingredients which are about to be injected into the patient’s body. It’s highly likely the physicians and nurses themselves don’t know the ingredients of each vaccine.

    So what’s in that vial? What’s coming through that needle?

    A Partial List of Ingredients

    Aluminum: Aluminum salts are used in some vaccine formulations as an adjuvant. An adjuvant is a substance added to vaccines to ostensibly enhance the immune response. Examples of aluminum salts in some vaccines are aluminum hydroxide, aluminum phosphate, alum (potassium aluminum sulfate) or mixed aluminum salts.

    In a 2011 study Canadian scientists Professor Christopher Shaw and Dr. Lucija Tomljenovic stated the following:

    “Aluminum is an experimentally demonstrated neurotoxin and the most commonly used vaccine adjuvant. In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation and associated neurological complications and may thus have profound and widespread adverse health consequences.”

    Multiple studies have shown that the intramuscularly injected aluminum vaccine adjuvant is absorbed into the systemic circulation and travels to different sites in the body, such as the brain, joints, and the spleen, where it accumulates and is retained for years post-vaccination.

    Mercury (thimerosal): Thimerosal is an ethyl mercury-based preservative used in vials that contain more than one dose of a vaccine (multi-dose vials) to prevent germs, bacteria and/or fungi from contaminating the vaccine. While in decline some flu vaccines and childhood vaccines in multi-dose vials still utilize thimerosal.

    Mercury is known to be a genotoxic agent, even in minute concentrations, which can damage the genetic information within a cell causing mutations, which may lead to cancer.

    A meta-analysis epidemiological study suggested thimerosal containing vaccines significantly increased the risk of neurodevelopmental disorders.

    A 2011 study suggested there may be higher rates of blood and brain mercury levels in monkeys exposed to vaccines containing thimerosal.

    The American Academy of Pediatrics and the U.S. Public Health Service (1999) published a joint statement that urged “all government agencies to work rapidly toward reducing children’s exposure to mercury from all sources.”

    Gelatin: Gelatin is used as a stabilizer in some vaccines licensed in the U.S. Stabilizers are added to vaccines to protect the active ingredients from degrading during manufacture, transport and storage.

    Gelatin is a protein obtained from cows or pigs and produced by the partial hydrolysis of collagen extracted by boiling animal parts such as cartilage, tendons, skin, bones and ligaments in water. Some people might have a severe allergic reaction to it.

    Certain vaccine viruses are grown on gelatin derived from the ligaments of pigs fed heavy doses of glyphosate in their feed. Gelatin comes from collagen which has lots of glycine.

    Gelatin is one of the most commonly identified causes of allergic reactions to vaccines.

    A 1999 Japanese study showed most anaphylactic reactions and some urticarial reactions to gelatin-containing measles, mumps, and rubella monovalent vaccines were associated with gelatin allergy. Based on these findings Japan removed gelatin from vaccines in 2000.

    Formaldehyde: Formaldehyde is used during the manufacture of some vaccines to inactivate viruses (like polio and hepatitis A viruses) or bacterial toxins (like diphtheria and tetanus toxins).

    Formaldehyde is a human carcinogen based on evidence from cancer studies in humans and is listed as aknown to be human carcinogen in the National Toxicology Program’s (NTP) Twelfth Report on Carcinogens(2011).

    Phenol/Phenoxyethanol: Phenoxyethanol is used in vaccines and biologics as a preservative to prevent microbial growth.

    A 2010 study, The relative toxicity of compounds used as preservatives in vaccines and biologics, assessed the relative cytotoxicity of the levels of the compounds commonly used as preservative in US licensed vaccines and found that for phenoxyethanol it was 4.6-fold, for phenol 12.2-fold and for Thimerosal >330-fold.

    They concluded, “None of the compounds commonly used as preservatives in US licensed vaccine/biological preparations can be considered an ideal preservative, and their ability to fully comply with the requirements of the US Code of Federal Regulations (CFR) for preservatives is in doubt.”

    Case reports (here, here and here) have suggested a link between phenoxyethanol and urticaria (hives), eczema and anaphylaxis.

    Triton X-100: Triton X –100 or octylphenol ethoxylate (OPE) is a surfactant (reducing the surface tension of liquids) and stabilizer present in some influenza vaccines.

    OPEs are endocrine disruptors and break down relatively easily into Octylphenols (OPs), which are more harmful. Endocrine disruptors can alter reproductive function, increase incidences of breast cancer, affect growth patterns and neurodevelopment in children and change immune function.

    Squalene: Squalene is a naturally-occurring substance derived primarily from shark liver oil. When combined with other ingredients it becomes an adjuvant, which, like aluminum, is added to vaccines to elicit a stronger immune response from the body.

    A 2000 study demonstrated that one intradermal injection of squalene adjuvant produced arthritis in rats.

    Some believe that Gulf War Syndrome was linked to the presence of squalene in certain lots of the anthrax vaccine.

    Beta-propiolactone: Beta-propiolactone (BPL) is a commonly used reagent for the inactivation of viruses for use in vaccine preparations. It has recently been used in the development of an inactivated SARS-CoV-2 vaccine preparation.

    Beta-propiolactone is a known carcinogen. Local sarcomas have been produced by subcutaneous injection of beta-propiolactone in rats. In the laboratory sarcomas and squamous papillomas in mice were produced by a single subcutaneous injection of a minute amount of beta-propiolactone.

    Polysorbate 80: Polysorbate 80 is present in some vaccines to stop the vaccine from separating into its component parts. In a PubMed study Polysorbate 80 was described as, “a ubiquitously used solubilizing agent that can cause severe nonimmunologic anaphylactoid reactions.”

    In a pharmacological study on mice and rats Polysorbate 80 produced, “mild to moderate depression of the central nervous system with a marked reduction in locomotor activity and rectal temperature, exhibited ataxia and paralytic activity and potentiated the pentobarbital sleeping time.”

    The results of that study concluded, “The results of the present study indicate that polysorbate 80 can neither be used as a solvent for isolated tissue experiments nor when considered for intravenous administration.”

    Another study from the American Association for Cancer Research (AACR) suggested the dietary emulsifier polysorbate 80 may induce low-grade inflammation which may contribute to metabolic diseases and increase the potential for development in colon cancer.

    Genetically modified yeast: S. cerevisiae, a species of yeast, is used in vaccines in a variety of ways. It is used as an adjuvant and now through genetic manipulation it is being used to create artificial antibodies

    Studies have suggested that genetically engineered yeast used in vaccines may be a contributing factor to autoimmune disorders.

    Monosodium Glutamate (MSG): Monosodium Glutamate is used in small amounts in some vaccines to keep them stable and protect them from losing potency even when exposed to heat and light.

    In a study that looked at rat fertility and MSG consumption the authors found there was a negative impact on the rats’ fertility.

    In another study it was noted that chronic MSG intake caused kidney dysfunction and renal oxidative stress in the animal model.

    Cells From Aborted Fetus: Fetal cell lines are used to grow viruses which are then collected from the cell cultures and processed further to produce the vaccine itself.

    The cell lines are propagated from lung tissue of mature aborted and used in the current manufacture of a number of routine vaccines, including measles, mumps and rubella (MMRV), diphtheria, tetanus, pertussis and polio, (DTaP-IPV), Hepatitis A and chickenpox.

    Aborted fetal cells are listed on vaccine package inserts as “Human Fetal Diploid Cells.” Two aborted fetal cell lines, WI-38 and MRC-5, have been grown under laboratory conditions since the 1960s. Diploid cells (WI-38, MRC-5) vaccines have their origin in induced abortions.

    The use of such cell lines can be profoundly objectionable to segments of the population who hold certain religious and/or philosophical beliefs.

    The Italian vaccine research and advocacy organization Corvelva released a study in 2019 regarding the use of aborted fetal cell lines in vaccines.

    In their summary they highlighted the following:

    The human genomic DNA contained in this vaccine is clearly, undoubtedly abnormal, presenting important inconsistencies with a typical human genome, that is, with that of a healthy individual.
    560 genes known to be associated with forms of cancer were tested and all underwent major modifications.
    There are variations whose consequences are not even known, not yet appearing in the literature, but which still affect genes involved in the induction of human cancer.
    What is also clearly abnormal is the genome excess showing changes in the number of copies and structural variants.
    Serum From Aborted Calf Fetus Blood: The purpose for the fetal bovine serum is to provide a nutrient broth for viruses to grow in cells.

    Humane Research Australia describes the process of how the blood is collected, “The blood is collected after the slaughter of a mature female cow, the mother’s uterus containing the calf fetus is removed during the evisceration process and transferred to the blood collection room. A needle is then inserted between the fetus’s ribs directly into its heart and the blood is vacuumed into a sterile collection bag.

    Only fetuses over the age of three months are used otherwise the heart is considered too small to puncture. Once collected, the blood is allowed to clot at room temperature and the serum separated through a process known as refrigerated centrifugation.”

    Beyond certain ethical considerations scientists have found that different bovine tissues contain different amounts of the BSE agent.

    Antibiotics: Antibiotics are used during the manufacturing process of some vaccines to stop bacteria growing and contaminating the vaccine.

    Antibiotics found in some vaccines include neomycin, streptomycin, polymyxin b, gentamicin and kanamycin.

    Polymyxin B comes with a warning that, “This medicine has not been fully studied in pregnant women. This medicine may cause kidney problems. This medicine may cause nerve problems”, as well as a laundry list of side effects.

    Similar warnings are found with streptomycin, neomycin, gentamicin, and kanamycin.

    A study out of Finland raised concerns about excessive antibiotic use in early childhood which may lead to weight gain and altered gut bacteria.

    What Else Could be in That Needle?

    The list above is not a complete account of all the ingredients found in various vaccine cocktails. A comprehensive manufacturers’ catalog of ingredients can be found here, here and here.

    The reality is that even a complete list issued by the producer doesn’t tell the entire story of what is found in vaccines.

    Using an Environmental Scanning Electron Microscope equipped with an X-ray microprobe a group of Italian scientists examined 44 samples of 30 different vaccines and found dangerous contaminants, including metal toxicants in 43 of the 44 samples tested.

    In the study, published in the International Journal of Vaccines and Vaccination, the researchers detected lead, chromium, nickel and other metals in every adjuvant sample tested.

    Additional metal contaminants identified in 25 of the human vaccines included platinum, silver, bismuth, iron, and chromium. Foreign impurities such as zirconium, hafnium, strontium, tungsten, antimony, bismuth, cerium and were also detected in many of the vaccines tested.

    The researchers commenting on their unexpected findings reported:

    The quantity of foreign bodies detected and, in some cases, their unusual chemical compositions baffled us. In most circumstances, the combinations detected are very odd as they have no technical use, cannot be found in any material handbook and look like the result of the random formation occurring….In any case, whatever their origin, they should not be present in any injectable medicament, let alone in vaccines, more in particular those meant for infants. [Emphasis added]

    When interviewed lead scientist Dr. Antonietta Gatti, of the National Council of Research of Italy and Scientific Director of Nanodiagnostics, explained that the discovery of vaccine impurities shocked the researchers:

    Those particles should not have been there. We had never questioned the purity of vaccines before. In fact, for us the problem did not even exist. All injectable solutions had to be perfectly pure and that was an act of faith on which it seemed impossible to have doubts. For that reason, we repeated our analyses several times to be certain. In the end, we accepted the evidence.

    Speculating on the potential consequences of these foreign impurities Dr. Gatti stated:

    The particles, be they isolated, aggregated or clustered, are not supposed to be there… Our tissues perceive these foreign bodies as potential enemies…Unfortunately, though, the particles we found in vaccines, are not biodegradable. So, all the macrophages’ efforts will be useless, and depending on the exact chemicals involved, the particles may be especially toxic. Cytokines and pro-inflammatory substances in general are released and granulated tissue forms, enveloping the particles. This provokes inflammation which, in the long run, if locally persistent, is known to be a precursor to cancer.

    Along with unlisted metal contaminants another unlisted contaminant was noted in some vaccines when a preliminary screening result from Microbe Inotech Laboratories Inc. detected glyphosate in the childhood vaccines they tested.

    Merck’s MMR II vaccine had 2.671 parts per billion (ppb) of glyphosate, Sanofi Pasteur’s DTap Adacel vaccine had 0.123 ppb, Novartis’ Influenza Fluvirin had 0.331 ppb, Glaxo Smith Kline’s HepB Energix-B vaccine had 0.325 ppb, Merck’s Pneumococcal Vax Polyvalent Pneumovax 23 had 0.107 ppb of glyphosate.

    These findings prompted Moms Across America to send a letter to the FDA, CDC, EPA,NIH and California Department of Health requesting that they test vaccines for glyphosate and recall contaminated vaccines.

    MIT scientist Dr. Stephanie Seneff remarked on the route by which glyphosate could get into vaccines:

    Collagen is a protein found in large amounts in the ligaments of cows, and these ligaments are often used in the production of gelatin. The MMR vaccine and flu vaccine viruses are grown as live cultures on gelatin sourced from cows fed high concentrations of glyphosate in their GMO Roundup­Ready feed.

    What to Do?

    Given the complex nature of the composition of vaccines and the paucity of information volunteered to the public on the manufacturing processes and ingredients that go into these products, how does one go about navigating this subject?

    Conventional wisdom might suggest, “Ask your doctor.” But how independent are these doctors?

    Where do you turn when you discover physicians and pediatricians, who have a legal duty to fully inform patients about vaccine risks and side effects, have ideological and material incentives to avoid presenting specific information that might cause a parent to question a vaccine?

    What about educational materials and advice from the agencies tasked with protecting public health? Can we trust the FDA and the CDC to provide detailed and unbiased information when it is known that they get substantial amounts of money from vaccine manufacturers?

    Informed consent is a principle in medical ethics and medical law that a patient must have sufficient information and understanding before making decisions about their medical care.This includes being given a thorough account of the risks and benefits of treatments, alternative treatments, the patient’s role in treatment, and their right to refuse treatment.

    Informed and individualized health care decisions about any product one puts into their or their children’s body starts with being fully informed with what is in that product.

    *

    Note to readers: Please click the share button above. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles.

    This article was originally published on Health Freedom Defense Fund.

    Featured image is from HFDF



    https://www.globalresearch.ca/do-you-know-what-vaccine/5839377
    Do You Know What’s in a Vaccine? Chemical Ingredients Addendum to the Childhood Vaccination Series All Global Research articles can be read in 51 languages by activating the Translate Website button below the author’s name. To receive Global Research’s Daily Newsletter (selected articles), click here. Click the share button above to email/forward this article to your friends and colleagues. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles. *** Over the last few decades, the number of chemicals added to foods and other products has skyrocketed. Chemicals are added to “enhance flavor”, make fruits and vegetables look fresh, extend the shelf life of packaged foods and for other invented reasons. A cornucopia of chemicals are also found in lotions and beauty products with the ostensible reason that these chemicals make beauty products feel, look, and smell nice. Along with this increase in heavily processed foods has come increased skepticism about the necessity of inserting chemical additives into everything we touch and taste. A significant and growing segment of the US population are beginning to examine the health consequences of ingesting and absorbing these chemical-laden products. This growing awareness about the adverse effects of ingesting and absorbing synthetic ingredients and the public’s understanding of the attendant health benefits of consuming products free from synthetic chemicals has prompted consumers to seek out organic ingredient-based items in their foods and skin lotions. More people are showing interest in knowing about the ingredients in their food and striving to ‘eat clean.’ This increased awareness is evidenced in the steady growth of the organic food industry and trends in the natural and organic cosmetic industry where demand is higher than ever. This same level of concern has begun to seep into the public conscience regarding a certain medical product that has mostly avoided scrutiny – the vaccine. Having been trained to accept that this product is a customary aspect of everyday life, most people haven’t given much thought to what’s inside the vaccine vials. Rarely will the vaccine ritual in the doctor’s office include a discussion about the ingredients which are about to be injected into the patient’s body. It’s highly likely the physicians and nurses themselves don’t know the ingredients of each vaccine. So what’s in that vial? What’s coming through that needle? A Partial List of Ingredients Aluminum: Aluminum salts are used in some vaccine formulations as an adjuvant. An adjuvant is a substance added to vaccines to ostensibly enhance the immune response. Examples of aluminum salts in some vaccines are aluminum hydroxide, aluminum phosphate, alum (potassium aluminum sulfate) or mixed aluminum salts. In a 2011 study Canadian scientists Professor Christopher Shaw and Dr. Lucija Tomljenovic stated the following: “Aluminum is an experimentally demonstrated neurotoxin and the most commonly used vaccine adjuvant. In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation and associated neurological complications and may thus have profound and widespread adverse health consequences.” Multiple studies have shown that the intramuscularly injected aluminum vaccine adjuvant is absorbed into the systemic circulation and travels to different sites in the body, such as the brain, joints, and the spleen, where it accumulates and is retained for years post-vaccination. Mercury (thimerosal): Thimerosal is an ethyl mercury-based preservative used in vials that contain more than one dose of a vaccine (multi-dose vials) to prevent germs, bacteria and/or fungi from contaminating the vaccine. While in decline some flu vaccines and childhood vaccines in multi-dose vials still utilize thimerosal. Mercury is known to be a genotoxic agent, even in minute concentrations, which can damage the genetic information within a cell causing mutations, which may lead to cancer. A meta-analysis epidemiological study suggested thimerosal containing vaccines significantly increased the risk of neurodevelopmental disorders. A 2011 study suggested there may be higher rates of blood and brain mercury levels in monkeys exposed to vaccines containing thimerosal. The American Academy of Pediatrics and the U.S. Public Health Service (1999) published a joint statement that urged “all government agencies to work rapidly toward reducing children’s exposure to mercury from all sources.” Gelatin: Gelatin is used as a stabilizer in some vaccines licensed in the U.S. Stabilizers are added to vaccines to protect the active ingredients from degrading during manufacture, transport and storage. Gelatin is a protein obtained from cows or pigs and produced by the partial hydrolysis of collagen extracted by boiling animal parts such as cartilage, tendons, skin, bones and ligaments in water. Some people might have a severe allergic reaction to it. Certain vaccine viruses are grown on gelatin derived from the ligaments of pigs fed heavy doses of glyphosate in their feed. Gelatin comes from collagen which has lots of glycine. Gelatin is one of the most commonly identified causes of allergic reactions to vaccines. A 1999 Japanese study showed most anaphylactic reactions and some urticarial reactions to gelatin-containing measles, mumps, and rubella monovalent vaccines were associated with gelatin allergy. Based on these findings Japan removed gelatin from vaccines in 2000. Formaldehyde: Formaldehyde is used during the manufacture of some vaccines to inactivate viruses (like polio and hepatitis A viruses) or bacterial toxins (like diphtheria and tetanus toxins). Formaldehyde is a human carcinogen based on evidence from cancer studies in humans and is listed as aknown to be human carcinogen in the National Toxicology Program’s (NTP) Twelfth Report on Carcinogens(2011). Phenol/Phenoxyethanol: Phenoxyethanol is used in vaccines and biologics as a preservative to prevent microbial growth. A 2010 study, The relative toxicity of compounds used as preservatives in vaccines and biologics, assessed the relative cytotoxicity of the levels of the compounds commonly used as preservative in US licensed vaccines and found that for phenoxyethanol it was 4.6-fold, for phenol 12.2-fold and for Thimerosal >330-fold. They concluded, “None of the compounds commonly used as preservatives in US licensed vaccine/biological preparations can be considered an ideal preservative, and their ability to fully comply with the requirements of the US Code of Federal Regulations (CFR) for preservatives is in doubt.” Case reports (here, here and here) have suggested a link between phenoxyethanol and urticaria (hives), eczema and anaphylaxis. Triton X-100: Triton X –100 or octylphenol ethoxylate (OPE) is a surfactant (reducing the surface tension of liquids) and stabilizer present in some influenza vaccines. OPEs are endocrine disruptors and break down relatively easily into Octylphenols (OPs), which are more harmful. Endocrine disruptors can alter reproductive function, increase incidences of breast cancer, affect growth patterns and neurodevelopment in children and change immune function. Squalene: Squalene is a naturally-occurring substance derived primarily from shark liver oil. When combined with other ingredients it becomes an adjuvant, which, like aluminum, is added to vaccines to elicit a stronger immune response from the body. A 2000 study demonstrated that one intradermal injection of squalene adjuvant produced arthritis in rats. Some believe that Gulf War Syndrome was linked to the presence of squalene in certain lots of the anthrax vaccine. Beta-propiolactone: Beta-propiolactone (BPL) is a commonly used reagent for the inactivation of viruses for use in vaccine preparations. It has recently been used in the development of an inactivated SARS-CoV-2 vaccine preparation. Beta-propiolactone is a known carcinogen. Local sarcomas have been produced by subcutaneous injection of beta-propiolactone in rats. In the laboratory sarcomas and squamous papillomas in mice were produced by a single subcutaneous injection of a minute amount of beta-propiolactone. Polysorbate 80: Polysorbate 80 is present in some vaccines to stop the vaccine from separating into its component parts. In a PubMed study Polysorbate 80 was described as, “a ubiquitously used solubilizing agent that can cause severe nonimmunologic anaphylactoid reactions.” In a pharmacological study on mice and rats Polysorbate 80 produced, “mild to moderate depression of the central nervous system with a marked reduction in locomotor activity and rectal temperature, exhibited ataxia and paralytic activity and potentiated the pentobarbital sleeping time.” The results of that study concluded, “The results of the present study indicate that polysorbate 80 can neither be used as a solvent for isolated tissue experiments nor when considered for intravenous administration.” Another study from the American Association for Cancer Research (AACR) suggested the dietary emulsifier polysorbate 80 may induce low-grade inflammation which may contribute to metabolic diseases and increase the potential for development in colon cancer. Genetically modified yeast: S. cerevisiae, a species of yeast, is used in vaccines in a variety of ways. It is used as an adjuvant and now through genetic manipulation it is being used to create artificial antibodies Studies have suggested that genetically engineered yeast used in vaccines may be a contributing factor to autoimmune disorders. Monosodium Glutamate (MSG): Monosodium Glutamate is used in small amounts in some vaccines to keep them stable and protect them from losing potency even when exposed to heat and light. In a study that looked at rat fertility and MSG consumption the authors found there was a negative impact on the rats’ fertility. In another study it was noted that chronic MSG intake caused kidney dysfunction and renal oxidative stress in the animal model. Cells From Aborted Fetus: Fetal cell lines are used to grow viruses which are then collected from the cell cultures and processed further to produce the vaccine itself. The cell lines are propagated from lung tissue of mature aborted and used in the current manufacture of a number of routine vaccines, including measles, mumps and rubella (MMRV), diphtheria, tetanus, pertussis and polio, (DTaP-IPV), Hepatitis A and chickenpox. Aborted fetal cells are listed on vaccine package inserts as “Human Fetal Diploid Cells.” Two aborted fetal cell lines, WI-38 and MRC-5, have been grown under laboratory conditions since the 1960s. Diploid cells (WI-38, MRC-5) vaccines have their origin in induced abortions. The use of such cell lines can be profoundly objectionable to segments of the population who hold certain religious and/or philosophical beliefs. The Italian vaccine research and advocacy organization Corvelva released a study in 2019 regarding the use of aborted fetal cell lines in vaccines. In their summary they highlighted the following: The human genomic DNA contained in this vaccine is clearly, undoubtedly abnormal, presenting important inconsistencies with a typical human genome, that is, with that of a healthy individual. 560 genes known to be associated with forms of cancer were tested and all underwent major modifications. There are variations whose consequences are not even known, not yet appearing in the literature, but which still affect genes involved in the induction of human cancer. What is also clearly abnormal is the genome excess showing changes in the number of copies and structural variants. Serum From Aborted Calf Fetus Blood: The purpose for the fetal bovine serum is to provide a nutrient broth for viruses to grow in cells. Humane Research Australia describes the process of how the blood is collected, “The blood is collected after the slaughter of a mature female cow, the mother’s uterus containing the calf fetus is removed during the evisceration process and transferred to the blood collection room. A needle is then inserted between the fetus’s ribs directly into its heart and the blood is vacuumed into a sterile collection bag. Only fetuses over the age of three months are used otherwise the heart is considered too small to puncture. Once collected, the blood is allowed to clot at room temperature and the serum separated through a process known as refrigerated centrifugation.” Beyond certain ethical considerations scientists have found that different bovine tissues contain different amounts of the BSE agent. Antibiotics: Antibiotics are used during the manufacturing process of some vaccines to stop bacteria growing and contaminating the vaccine. Antibiotics found in some vaccines include neomycin, streptomycin, polymyxin b, gentamicin and kanamycin. Polymyxin B comes with a warning that, “This medicine has not been fully studied in pregnant women. This medicine may cause kidney problems. This medicine may cause nerve problems”, as well as a laundry list of side effects. Similar warnings are found with streptomycin, neomycin, gentamicin, and kanamycin. A study out of Finland raised concerns about excessive antibiotic use in early childhood which may lead to weight gain and altered gut bacteria. What Else Could be in That Needle? The list above is not a complete account of all the ingredients found in various vaccine cocktails. A comprehensive manufacturers’ catalog of ingredients can be found here, here and here. The reality is that even a complete list issued by the producer doesn’t tell the entire story of what is found in vaccines. Using an Environmental Scanning Electron Microscope equipped with an X-ray microprobe a group of Italian scientists examined 44 samples of 30 different vaccines and found dangerous contaminants, including metal toxicants in 43 of the 44 samples tested. In the study, published in the International Journal of Vaccines and Vaccination, the researchers detected lead, chromium, nickel and other metals in every adjuvant sample tested. Additional metal contaminants identified in 25 of the human vaccines included platinum, silver, bismuth, iron, and chromium. Foreign impurities such as zirconium, hafnium, strontium, tungsten, antimony, bismuth, cerium and were also detected in many of the vaccines tested. The researchers commenting on their unexpected findings reported: The quantity of foreign bodies detected and, in some cases, their unusual chemical compositions baffled us. In most circumstances, the combinations detected are very odd as they have no technical use, cannot be found in any material handbook and look like the result of the random formation occurring….In any case, whatever their origin, they should not be present in any injectable medicament, let alone in vaccines, more in particular those meant for infants. [Emphasis added] When interviewed lead scientist Dr. Antonietta Gatti, of the National Council of Research of Italy and Scientific Director of Nanodiagnostics, explained that the discovery of vaccine impurities shocked the researchers: Those particles should not have been there. We had never questioned the purity of vaccines before. In fact, for us the problem did not even exist. All injectable solutions had to be perfectly pure and that was an act of faith on which it seemed impossible to have doubts. For that reason, we repeated our analyses several times to be certain. In the end, we accepted the evidence. Speculating on the potential consequences of these foreign impurities Dr. Gatti stated: The particles, be they isolated, aggregated or clustered, are not supposed to be there… Our tissues perceive these foreign bodies as potential enemies…Unfortunately, though, the particles we found in vaccines, are not biodegradable. So, all the macrophages’ efforts will be useless, and depending on the exact chemicals involved, the particles may be especially toxic. Cytokines and pro-inflammatory substances in general are released and granulated tissue forms, enveloping the particles. This provokes inflammation which, in the long run, if locally persistent, is known to be a precursor to cancer. Along with unlisted metal contaminants another unlisted contaminant was noted in some vaccines when a preliminary screening result from Microbe Inotech Laboratories Inc. detected glyphosate in the childhood vaccines they tested. Merck’s MMR II vaccine had 2.671 parts per billion (ppb) of glyphosate, Sanofi Pasteur’s DTap Adacel vaccine had 0.123 ppb, Novartis’ Influenza Fluvirin had 0.331 ppb, Glaxo Smith Kline’s HepB Energix-B vaccine had 0.325 ppb, Merck’s Pneumococcal Vax Polyvalent Pneumovax 23 had 0.107 ppb of glyphosate. These findings prompted Moms Across America to send a letter to the FDA, CDC, EPA,NIH and California Department of Health requesting that they test vaccines for glyphosate and recall contaminated vaccines. MIT scientist Dr. Stephanie Seneff remarked on the route by which glyphosate could get into vaccines: Collagen is a protein found in large amounts in the ligaments of cows, and these ligaments are often used in the production of gelatin. The MMR vaccine and flu vaccine viruses are grown as live cultures on gelatin sourced from cows fed high concentrations of glyphosate in their GMO Roundup­Ready feed. What to Do? Given the complex nature of the composition of vaccines and the paucity of information volunteered to the public on the manufacturing processes and ingredients that go into these products, how does one go about navigating this subject? Conventional wisdom might suggest, “Ask your doctor.” But how independent are these doctors? Where do you turn when you discover physicians and pediatricians, who have a legal duty to fully inform patients about vaccine risks and side effects, have ideological and material incentives to avoid presenting specific information that might cause a parent to question a vaccine? What about educational materials and advice from the agencies tasked with protecting public health? Can we trust the FDA and the CDC to provide detailed and unbiased information when it is known that they get substantial amounts of money from vaccine manufacturers? Informed consent is a principle in medical ethics and medical law that a patient must have sufficient information and understanding before making decisions about their medical care.This includes being given a thorough account of the risks and benefits of treatments, alternative treatments, the patient’s role in treatment, and their right to refuse treatment. Informed and individualized health care decisions about any product one puts into their or their children’s body starts with being fully informed with what is in that product. * Note to readers: Please click the share button above. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles. This article was originally published on Health Freedom Defense Fund. Featured image is from HFDF https://www.globalresearch.ca/do-you-know-what-vaccine/5839377
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    Do You Know What’s in a Vaccine? Chemical Ingredients
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  • California Institute of Technology - Quantum entanglement of photons doubles microscope resolution:

    https://phys.org/news/2023-05-quantum-entanglement-photons-microscope-resolution.html

    #QuantumEntanglement #Entanglement #Biphoton #Photons #DawesLimit #HeisenbergLimit #OpticalResolution #Optics #QuantumMechanics #QuantumMicroscopyByCoincidence #QMC #LASER #Microscopy #QuantumPhysics #Physics
    California Institute of Technology - Quantum entanglement of photons doubles microscope resolution: https://phys.org/news/2023-05-quantum-entanglement-photons-microscope-resolution.html #QuantumEntanglement #Entanglement #Biphoton #Photons #DawesLimit #HeisenbergLimit #OpticalResolution #Optics #QuantumMechanics #QuantumMicroscopyByCoincidence #QMC #LASER #Microscopy #QuantumPhysics #Physics
    PHYS.ORG
    Quantum entanglement of photons doubles microscope resolution
    Using a "spooky" phenomenon of quantum physics, Caltech researchers have discovered a way to double the resolution of light microscopes.
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  • The cross section of a blade of grass, stained for the microscope. The smiley faces are the channels that the water is drawn up through.

    .

    .

    ????: The Mind Unleashed
    The cross section of a blade of grass, stained for the microscope. The smiley faces are the channels that the water is drawn up through. . . ????: The Mind Unleashed
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  • Teach me some scientific facts "Mr. computer"

    C-GPT:
    The human brain contains about 100 billion neurons. These neurons communicate with each other through electrical and chemical signals, allowing us to think, feel, and perceive the world around us.

    The Earth's atmosphere is composed of approximately 78% nitrogen, 21% oxygen, and 1% other gases, including carbon dioxide, neon, and helium.

    The speed of light is about 299,792,458 meters per second. This means that light can travel around the Earth's equator almost 7.5 times in just one second!

    The smallest living organisms on Earth are called bacteria. These single-celled organisms are so tiny that they can only be seen with a microscope.

    The largest living organism on Earth is a fungus called Armillaria ostoyae. It covers an area of approximately 2,200 acres in the Malheur National Forest in Oregon.

    I hope you find these scientific facts interesting!
    Teach me some scientific facts "Mr. computer" C-GPT: The human brain contains about 100 billion neurons. These neurons communicate with each other through electrical and chemical signals, allowing us to think, feel, and perceive the world around us. The Earth's atmosphere is composed of approximately 78% nitrogen, 21% oxygen, and 1% other gases, including carbon dioxide, neon, and helium. The speed of light is about 299,792,458 meters per second. This means that light can travel around the Earth's equator almost 7.5 times in just one second! The smallest living organisms on Earth are called bacteria. These single-celled organisms are so tiny that they can only be seen with a microscope. The largest living organism on Earth is a fungus called Armillaria ostoyae. It covers an area of approximately 2,200 acres in the Malheur National Forest in Oregon. I hope you find these scientific facts interesting!
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  • The nuggets came from two national fast-food chains in Jackson. The three researchers selected one nugget from each box, preserved, dissected, and stained the nuggets, then looked at them under a microscope.

    The first nugget was about half muscle, with the rest a mix of fat, blood vessels, and nerves. Close inspection revealed cells that line the skin and internal organs of the bird, the authors wrote in the American Journal of Medicine.

    The second nugget was only 40 percent muscle, and the remainder was fat, cartilage, and pieces of bone.

    "We all know white chicken meat to be one of the best sources of lean protein available and encourage our patients to eat it," lead author Dr. Richard D. deShazo of the University of Mississippi Medical Center in Jackson said.

    "What has happened is that some companies have chosen to use an artificial mixture of chicken parts rather than low-fat chicken white meat, batter it up and fry it and still call it chicken," deShazo told Reuters Health.

    "It is a chicken by-product high in calories, salt, sugar, and fat that is very unhealthy. Even worse, it tastes great, and kids love it, and it is marketed to them."

    The nuggets he examined would be OK to eat occasionally, but he worries that since they are cheap, convenient, and taste good, kids eat them often. His grandchildren "beg" for chicken nuggets all the time, and he compromises by making them at home by pan-frying chicken breasts with a small amount of oil, deShazo said.
    The nuggets came from two national fast-food chains in Jackson. The three researchers selected one nugget from each box, preserved, dissected, and stained the nuggets, then looked at them under a microscope. The first nugget was about half muscle, with the rest a mix of fat, blood vessels, and nerves. Close inspection revealed cells that line the skin and internal organs of the bird, the authors wrote in the American Journal of Medicine. The second nugget was only 40 percent muscle, and the remainder was fat, cartilage, and pieces of bone. "We all know white chicken meat to be one of the best sources of lean protein available and encourage our patients to eat it," lead author Dr. Richard D. deShazo of the University of Mississippi Medical Center in Jackson said. "What has happened is that some companies have chosen to use an artificial mixture of chicken parts rather than low-fat chicken white meat, batter it up and fry it and still call it chicken," deShazo told Reuters Health. "It is a chicken by-product high in calories, salt, sugar, and fat that is very unhealthy. Even worse, it tastes great, and kids love it, and it is marketed to them." The nuggets he examined would be OK to eat occasionally, but he worries that since they are cheap, convenient, and taste good, kids eat them often. His grandchildren "beg" for chicken nuggets all the time, and he compromises by making them at home by pan-frying chicken breasts with a small amount of oil, deShazo said.
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  • Check this out. I found this old Tasco 450x microscope I got as a young boy about 1971. Its in the original box and all but a couple of the original contents are still there. You can tell by my old birthday photo how excited i was. I am such a nerd. Also everything works and its in great shape.
    Check this out. I found this old Tasco 450x microscope I got as a young boy about 1971. Its in the original box and all but a couple of the original contents are still there. You can tell by my old birthday photo how excited i was. I am such a nerd. Also everything works and its in great shape.
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  • This is a microscope image of beach blade grass (Ammophila arenaria). It has small cells that seem to smile when you see them. beautiful nature.
    This is a microscope image of beach blade grass (Ammophila arenaria). It has small cells that seem to smile when you see them. beautiful nature.
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  • If you get the message, hang up. For psychedelic drugs are simply instruments, like microscopes, telescopes and telephones.

    The biologist does not sit with his eye permanently glued to the microscope, he goes away and works on what he has seen.
    - Alan Watts

    #philosophy #psychadelics #psychadelic #mushrooms #acid
    If you get the message, hang up. For psychedelic drugs are simply instruments, like microscopes, telescopes and telephones. The biologist does not sit with his eye permanently glued to the microscope, he goes away and works on what he has seen. - Alan Watts #philosophy #psychadelics #psychadelic #mushrooms #acid
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  • Have you taken a much closer look at Koalas’ hands? You would see that they have fingerprints that are nearly identical, just like humans.
    In fact, those are so alike that even detailed investigation under a microscope can effortlessly differentiate when it involves loopy, spinning ridges on koalas’ fingers from your own.

    https://www.mcgill.ca/oss/article/did-you-know/koalas-have-fingerprints-just-humans
    Have you taken a much closer look at Koalas’ hands? You would see that they have fingerprints that are nearly identical, just like humans. In fact, those are so alike that even detailed investigation under a microscope can effortlessly differentiate when it involves loopy, spinning ridges on koalas’ fingers from your own. https://www.mcgill.ca/oss/article/did-you-know/koalas-have-fingerprints-just-humans
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  • Tears are different under the microscope depending on their case!

    One of the awesomee facts people are unaware of is that it seems that our tears are transparent in color and similar for every situation—from happiness to sadness.
    However, that’s actually far from reality. It was discovered that our tears for different emotions differ from one another!

    #Awesomee
    #AF
    #Facts
    Don't forget to like and follow for AweSomee facts on a daily basis!

    Source:
    https://spectaclesms.com/blogs/tears
    Tears are different under the microscope depending on their case! One of the awesomee facts people are unaware of is that it seems that our tears are transparent in color and similar for every situation—from happiness to sadness. However, that’s actually far from reality. It was discovered that our tears for different emotions differ from one another! #Awesomee #AF #Facts Don't forget to like and follow for AweSomee facts on a daily basis! Source: https://spectaclesms.com/blogs/tears
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