Tal Zaks, Former Chief Scientist at Moderna, Speaks of Nanomedicine, Personalized Vaccines and Genetic Engineering in 2017

Scientist quote/unquote: “hacking the software of life.”

Tal Zaks, former Chief Medical Officer at Moderna (currently partnering with Orbimed) – gives us another look at their terminology of “hacking the software of life”, i.e. – changing/modifying our genes.

Piggybacking off of Klaus Schwab’s statements that gene-editing changes YOU, not to mention Craig Venter’s (of the Human Genome Project) admission that:

“It’s pretty stunning when you just replace the DNA software in the cell, and the cell instantly starts reading that new software, starts making a whole different set of proteins. And within a short while, all the characteristics of the first species disappear. And a new species emerges from this software that controls that cell going forward.”

Craig Venter of the NIH and Human Genome: Creating Synthetic Life | ” – trying to design what we want biology to do”

– it is clear that, by definition, “rewriting the genetic code” changes what it means to be human – or changes whatever species is being modified. Craig Venter himself says that a “new species emerges from this software”.

So while these doctors and scientists try to sugarcoat these ill-conceived endeavors (even if they were born of good intentions initially… “the road to hell is paved with good intentions”), the attempts at genetically changing our DNA have grave consequences; not only on the physical-molecular level, but on the conscious-soul level as well.

Here, Tal Zaks, in a Tedx Talk from November 2017, specifically mentions vaccines (a total of 17 times in a 10 minute presentation) to administer this genetic-changing software. In addition, he also alludes to collecting DNA in order to make “personalized vaccines”. An endeavor that DARPA is also invested in:

DNA Script Partners with Moderna to Develop On-Demand Vaccines and Therapeutics for DARPA

SOUTH SAN FRANCISCO, Calif., and PARIS | April 27, 2021

[ https://www.dnascript.com/press-releases/dna-script-partners-with-moderna-to-develop-on-demand-vaccines-and-therapeutics-for-darpa/ ]

“Rewriting the Genetic Code” – Tal Zaks (2017)

Source: odysee | @RedPillman | Rewriting the Genetic Code

Full transcript below. Some embellishment has been added for emphasis.

Tal Zaks: “So I started my professional life about thirty years ago as a nurse and the pediatric intensive care unit.

And I remember this one infant, let’s call him Jonathan, who came in really really ill. Seemed to have a rare genetic defect, but in those days, gene diagnosis was still in its infancy so we couldn’t really figure out what’s wrong with him.

And in the years since, as I’ve trained as a physician scientist, we’ve been living in this phenomenal digital and scientific revolution. And I’m here today to tell you that we’re actually hacking the software of life. And that it’s changing the way we think about prevention and treatment of disease.

So here’s all the biology you need to know in 30 seconds. Our body is made out of organs, our organs are made out of cells, and in every cell there’s this thing called “messenger RNA” or mRNA for short, that transmits the critical information from the DNA, our genes, to the protein, which is really the stuff we’re all made of.

This is the critical information that determines what a cell will actually do. And so we think of it like an operating system. And it’s not just in every cell of our body. It’s actually in every cell of every organism of life. It’s the same thing.

And so, if you could actually change that, which we call the software of life, you could introduce a line of code, or change a line of code, it turns out that has profound implications for everything from the flu, to cancer. And I’m going to demonstrate that with three short examples.

Let’s start with the flu. So many of us get a vaccine. What is a vaccine? It is an injection in our arm where we get bits and pieces of the virus; the protein, and that teaches our immune system to recognize the virus and so when we get infected we’re not sick.

Now imagine if instead of giving the protein, we would give the instructions on how to make the protein. How the body can make its own vaccine. That’s an mRNA vaccine.

And here’s what it looks like from the cell.”

Image Source: Tal Zaks / Tedx Talks

“So the traditional approach has protein floating around your cells. An mRNA vaccine approach has the cells themselves in your own body making the vaccine.

What’s more alarming: a stranger prowling the neighborhood, or somebody who’s just broke into your ground-floor, and tripped the alarm?

That’s what happens with an mRNA vaccine. You’re tripped the alarm wire and now the cell is dialing 9-1-1. It’s calling the police at the same time as it’s making the protein and saying, ‘that’s the bad guy’.

That’s how an mRNA works. And for the last several years we’ve shown this actually works in a whole multitude of animal models. Earlier this year we published the first actual study in people. And it actually works in people.

We took a group of volunteers and injected them with a messenger RNA vaccine against a variant of flu/influenza. And all of these volunteers got the immune response we were hoping to see. The side-effect profile was pretty benign, what you would see with any normal type vaccine.

So we’ve proven the principle, this actually can work. It works in people and now we’re going to be developing a whole slew of vaccines against diseases for which we don’t have one. So that’s infectious disease.

Now for the second example, let’s talk for a minute about cancer. Horrible disease. Cancer has affected the lives of many of us and will affect the lives of many more of us as we age.

The problem with cancer at the cellular level is that the DNA is screwed up. You’ve got these mutation on this screwed up DNA, leads up to screwed up information that makes screwed up protein. And so the cell loses control.

Now, how do you figure out what is actually screwed up? Well, you got to figure out the whole sequence, right?

It took us decades and billions of dollars to sequence the human genome, and we’ve done that. We achieved that in 2003. And now we’re less than 15 years later, and it takes us a week. And we can do it for every patient. So now we can go and figure out what exactly is screwed up in a patient, and we can use that information to make a vaccine.

We take that information, say a patient with lung cancer, and we take it – we take the biopsy, we figure out the sequence, we figure out their immune system, we – and that all becomes information. It goes up in the cloud into a bioinformatic algorithm and then automatically makes a vaccine that we administer into their normal tissue; into the muscle to try and wake up their immune system.

Now the challenge, of course, is that every person’s cancer is different. Mutation happened by random chance. And so to do this you have to make it personalized.

So this is me, but if every patient is different, what we’re going to have to do is make a personalized cancer vaccine for every patient. And that’s exactly what we’ve started to do. Every patient gets a vaccine that’s based on the sequence and their own tumor.

So when we started to do this a couple years ago, my CEO stopped by one evening and said, “Tal, I get the idea but is this going to work?” And I said, “Look, Stefan. I don’t know, but we’ve got all the pieces to try and answer the question so we should try.”

And today I can tell you that I still don’t know if it’s going to work. But I know we’re able to actually run the experiment. Earlier this week the first patient was treated with a personalized cancer vaccine we made just for her.

So in the months and years to come we will know the answer of whether we can actually wake the immune system against somebody’s cancer with a personalized cancer vaccine so stay tuned.

I’m gonna finish with a third example of something called “methylmalonic acidemia” or MMA for short. Now the name doesn’t matter. Okay? This is just a disease that is caused by an enzyme that’s critical for metabolism. And children are born and they lack this one crucial gene. And so their body is not able really to fight infection properly or anytime they have any sort of stress, their body goes into crisis. They have one gene that’s gone awry and it causes a really significant disease.

If you look at what happens over time, for these children, about 1/3 of them don’t make it to the age of 10. You see here the survival curve whether the gene is completely lost or whether there’s just an aberration in it, the survival is impaired.

And, what do we do? Well there’s not much you can do because the missing protein is actually missing inside their cells. So what do we do? Well, here’s what we do. We take out their liver and we transplant the liver from a donor that is healthy and normal into these kids.

Think about it. They’re missing one critical piece of information and what we do is transplant an entire organ. Well, it fixes the problem, but what if there’s a better way? What if we could fix the missing information?

So based on innovations, nanomedicine, a new class of invention that Bob Langer across the river at MIT in Cambridge has been inventing, we’re now able to package this information and messenger RNA with a goal of giving it as an infusion, and then having it go to the liver to replace that missing information.

Is this going to work? Well we know the biology works. So together with the National Institutes of Health, we’ve studied this in a mouse model and this mouse has been engineered to have the exact same problem that the kids have. They’re lacking the one – the same gene. And you can see in the red line what happens to these mice when they’re born. Pretty much immediately they die. They cannot cope with stress. But if you inject messenger RNA that codes for the one missing protein that replaces that information, these mice, all of them survive, as you can see in the green line. And if you look at them they not only survive, they’re actually growing, they’re gaining weight, they look like they’re healthy littermates.

We’re hoping to start the clinical trial in the near future and the idea is the same thing here. If you think about what it is we’re trying to do, we’ve taken information and our understanding of that information and how that information is transmitted in a cell, and we’ve taken our understanding of medicine and how to make drugs and we’re fusing the two. We think of it as information therapy.

I started by telling you about Jonathan and 30 years ago, and I was a nurse in the intensive care unit, I worked two night shifts, and Jonathan came in when he was about 12 months old and very quickly became dependent on a ventilator. And for the next 15 months or so, every time I came into the unit he was my patient to care for. You know, bathe, feed, treat, play with – he couldn’t talk, he was on a ventilator, but he was very much alive and you could tell – you could play with him, his eyes would – would follow me. After a while he would recognize me. Until one day I came into the unit for my shift and he was no longer there. He had died because of an infection in between shifts.

Imagine a world where we cannot just diagnose, but we can actually use the information to create vaccines to wake up the immune system to something like cancer and to fix the missing information for children with diseases like Jonathan, so that they can leave the ICU and live a healthy life.

Thank you.”

What is “nanomedicine”?

“Nanomedicine is defined as the medical application of nanotechnology. Nanomedicine can include a wide range of applications, including biosensors, tissue engineering, diagnostic devices, and many others. In the Center for Nanomedicine at Johns Hopkins, we focus on harnessing nanotechnology to more effectively diagnose, treat, and prevent various diseases.”

[ https://cnm-hopkins.org/what-is-nanomedicine/ ]

Interestingly, but not surprisingly, Johns Hopkins was the organization that the WEF (World Economic Forum / Klaus Schwab – famous for the “Great Reset” agenda) chose to moderate the EVENT 201 Plandemic Pandemic exercise, with the help of the Bill and Melinda Gates Foundation…

And while, of course, Mr. Zaks ends his speech high-lighting the beneficial aspects of a “gene-editing vaccine” and reminds the audience that it is to “cure cancer” or any other number of diseases, we must be alert to alternative motives and the implications of what could arise from such technological tampering of the human genome, not to mention a collection of the population’s DNA in a database – to control and alter at their discretion.

Now aside from those chilling prospects, is it worth it to forever alter a human being, and what it means to be human, by injecting them with genetic changing software? What possibilities might arise from such an endeavor? Are we SURE that they have our best interest in mind? (that is a rhetorical question, by the way… because of course they don’t) If they can change us as a species, then it follows suit that it can change our emotions, our thoughts, even our very purpose.

There are some things in life which should not be meddled with. “Life” itself, is definitely one of them.

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Featured image by Gerd Altmann from Pixabay

Dr. Michael Yeadon (Former Pfizer Chief Scientist) Warns Pregnant Women of the Dangers of Taking The Experimental COVID Vaccine

Study on women showed “vaccine induced autoimmune attack, on their own placenta.”

Dr. Michael Yeadon, a former Chief Scientist and VP of the Allergy and Respiratory Unit of Pfizer, has been very outspoken in his assessment of these “vaccines”, and has called this agenda out several times for being deliberate crimes against humanity. The following video below is an explanation and warning to people – specifically for women who are pregnant or who are of child-bearing potential, to avoid these dangerous injections.

Source: bitchute | WHAT IS TRUTH?/WAS IST WAHRHEIT? |
3 THINGS WOMEN SHOULD KNOW ABOUT THE COVID JAB – DR. MICHAEL YEADON

The following text is transcribed from the above video with some embellishment added for emphasis. All words are from Dr. Michael Yeadon.

“You’re being lied to. I’m being lied to. We’re not being treated like adults. And the authorities are not giving us full information about the, the risks of these products. And so I’m going to try and do a non-science presentation, um, because I really want to speak to you who are probably not scientists. You’ll be a lay audience. So I’m going to do my best.

So, uh, three things to tell you about my concerns about the impact of these vaccines in reproductive health, fertility and pregnancy.

The first thing, is so obvious, that you’ll agree with me when I tell you. And that’s, we never, EVER, give experimental medicines to pregnant women. Why do we not do that? Well, you’ll probably will have heard of the word ‘thalidomide’. 60 years ago, through, I think an ignorant failure of medicines regulation, we were more exposed to a new product for morning sickness called thalidomide. And it led to at least 10,000 birth malformations. And we didn’t know at the time, that the studies they were doing at the time simply wouldn’t pick out thalidomide as the actual toxin in the womb.

And I think it also taught us that babies are not safe and protected inside the uterus, which is what we used to think. But in fact, there are a miracle of minute development, critical stages, especially in the early stages, where if they interfered with biochemicals or something else, it can change the course of development to that child irreparably.

So that’s the thing to tell you. You never ever give, really inadequately tested medicines, medicinal products, to a pregnant woman. And that’s exactly what is happening. Our government is urging pregnant women, and women of child-bearing age, to get vaccinated. And they’re telling them they’re safe. And that’s a lie. Because those studies have simply not been done.

So reproductive toxicology has not been undertaken with any of these products. Certainly not a full battery of tests that you would want. So here we are, dosing potentially hundreds of millions of women of child-bearing potential, with products which are untested in terms of impacts on fertilization and development of a baby. That’s bad enough, because what that tells me is that there’s recklessness; no one cares. The authorities do not care what happens. But it’s much worse than that. And remember, I’m a toxicologist as well as a research scientist.

Two things to tell you.

The first only came to light because of a Freedom of Information request made by somebody to the Japanese medicines regulator. So the Japanese medicines regulator had required Pfizer to do a study where they looked at how the vaccine distributed around the body, in this case of a rat, over time. It’s a distribution pharmacokinetic study. And they were not required in America or Europe, because that’s not what you do with vaccines. Another – for another day. But the Japanese regulators required it.

Now I’ve seen a copy of that report, and I’m entirely able to read and interpret it. And to my horror, what we find is the vaccine doesn’t just distribute around the body and then wash out again. Which is what you hope. It concentrates in ovaries of rats. And it concentrates, at least, twenty-fold over the concentration in other background tissues like muscles.

Um, what’s it doing there? Well I don’t know. You don’t want this product in your ovaries. It’s simply not necessary to induce immunity to have a vaccine in your ovaries. And, as it’s concentrating in the ovaries, getting higher concentrations over time, they have not even defined what the maximum levels are or when that occurs.

So, so now we’ve got a second problem; that the vaccine, at least in rats, distributes in the ovaries. And I’ll tell you, a general rule of thumb in toxicology, is if you don’t have any data to counter contradict what you’ve learned, that’s the assumption you make for humans. So my assumption at the moment, is that’s what’s happening to every female who’s been given these vaccines. These vaccines are concentrating in her ovaries.

That’s very worrying. So we don’t know what that will do, but it cannot be benign. And it could be seriously harmful. Because the vaccines will then express the coronavirus spike protein and we know that there are unwanted biologies from that spike proteins. That’s the second one.

I’ve got another one now, and it’s even worse! Because it’s actually, this time an experiment in humans. In females.

I wrote with a German doctor 8 months ago, a petition to the European Medicines Agency. And amongst several concerns we had, one was that the spike protein is faintly similar, not very strongly, but faintly similar to an essential protein in your placenta. Something that’s absolutely required for both fertilization and formation and maintenance of the placenta. So you can’t get pregnant and have a successful pregnancy if this protein is damaged in any way. And we noticed that the coronavirus spike protein is similar. Similar enough that I would worry.

And I wanted them to do some experiments, hopefully to rule out the possibility that when you vaccinate the person, who then makes spike proteins, and they develop an immune response against this spike protein; my worry was that there would be an echo. You know. A faint signal that would potentially bind this similar protein in the placenta. And the studies just came out a few weeks ago and it says, exactly, what I was worried about.

15 women were given Pfizer vaccines, they drew blood samples every few days, and they measured antibodies against the spike protein; which took several weeks to appear. They also measured antibodies against the placenta. And they found within the first 1-4 days an increase of two and a half to three times – a 300% increase, in the antibodies against their own placenta. In the first 4 days. Um, so, I’m sorry to say this, but that is a vaccine induced autoimmune attack, on their own placenta.

And I think you can only expect that that is happening in every woman of child-bearing potential, is generating antibodies against this critical protein required for fertilization and successful pregnancy. Now, what the effect will be we can’t be certain. Again it can’t be benign. I don’t know whether it’s enough to cause first trimester losses. But I would think it would, because I’ve looked at the literature, and women who are unfortunate enough to have what are called autoimmune diseases, tend to have a higher rate of first trimester losses. And what this vaccine’s done is induced an autoimmune response.

So, I’m here to warn you that if you are of child-bearing potential, or younger – so, not at menopause, I would strongly recommend you do not accept these vaccines. Thank you.”

Thank you to Dr. Michael Yeadon for bringing this awareness and research to the forefront and warning people of the potential dangers to this COVID vaccine.

I also want to point out that most vaccine trials take 10-15 years, if not more, to determine safety and efficacy. Yet with the COVID vaccine, it was developed in 2 MONTHS since word of the outbreak hit (some sources are claiming it is because of the wonderful advancements being made in tech and the “stupendous foresight of the NIH” to predict a similar outbreak would happen… if that’s what you would like to believe…) and the clinical trials started soon after. With emergency authorized use only, NOT APPROVED, 9 months later.

With this in mind, even if it becomes “approved” – in which this little caveat has caused more drama and confusion than what was necessary – are we going to still continue to trust the FDA, the CDC, NIH, NIAID on these incredibly unnecessary vaccines, when we can now see the results of this rushed mRNA/spike protein experiment? Not to mention, there are treatment regiments available that are KNOWN to treat this illness, in which the EUA would not be required since under their own regulations they state:

“Under an EUA, FDA may allow the use of unapproved medical products, or unapproved uses of approved medical products in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions when certain statutory criteria have been met, including that there are no adequate, approved, and available alternatives.”https://www.fda.gov/vaccines-blood-biologics/vaccines/emergency-use-authorization-vaccines-explained

Doctors have proven, IN COURT, that Ivermectin, an already approved medicine, works and nutraceutical bundles are beneficial in treating these respiratory syndromes. Yet they are being SUPPRESSED by the very health agencies that are promoting vaccines every where we turn, even though the vaccines are not approved and are causing thousands upon thousands of side effects and deaths.

Please do your research and use critical thinking and discernment. Doctors like Michael Yeadon get nothing from trying to save your life and help you (except censorship and ridicule from the mainstream media and big tech platforms) and shows genuine concern for our well-being. While pharmaceutical companies have gained BILLIONS from pushing these experimental vaccines onto the population.

Thank you again to all of the sincere doctors/scientists/healthcare workers/researchers who are bringing all of this information to light.