Does MRNA Technology Edit Our Genetic Code?

The War on Cancer has been raging for over a century, and Tal Zaks may have the biggest breakthrough yet.

His idea, to go straight to the source of the problem and edit the genetic code that causes the body to produce cancerous cells, could save millions of lives without a single surgery or chemotherapy regimen.

Tal Zaks is the Chief Medical Officer of Moderna Therapeutics.

That’s the description on this TED talk, it says it fairly clearly that he’s editing the genetic code with MRNA technology, which Facebook banned people for saying even though Mark Zuckerberg said it himself and censored himself saying it.

We are actually hacking the software of life” was what he said, and that he called it “information therapy”.

Here’s an article from around the same time, 2018, from the Sloan Kettering cancer center, where they say they just found out that some types of cancer may be caused by the MRNA messenger code, rather than the DNA.

There’s a problem with the MRNA making a certain type of tumor suppressing protein and they only just figured that out, maybe, and have no idea if hitting it with a vaccine software update will fix the problem(s).

That guy literally said it took them years and years to map the whole human genome, but now they can do it in a week, and make a new vaccine for each individual person, and each individual tumor.

Really? They can just do that now, rewrite the genetic code of anyone’s DNA or RNA, and make cancer just disappear? No, they haven’t tested it yet.

The population of the world are the test subjects for this new MRNA vaccine technology, they didn’t even start with animal trials first.

80% of people in the Moderna trials of the covid vaccine had fairly noticeable side effects, and then Bill Gates censored himself saying that.

They’re going to send in a piece of MRNA code that tells the cells to make a protein that exists on the spike proteins of the coronavirus that they made in the Wuhan lab, and then it will make them.

How long will it keep making those proteins for? Nobody knows. They say it will just harmlessly move out of the cell, and stop doing what it does, after forcing it’s way into them, but I don’t think they even know what will happen.

This guy is talking about using these codes to repair organs, repair spinal cords maybe. Anything, everything, but first, you need a guinea pig, or billions of them.

Skeptics are saying they made the virus to kill you, and they’re making the vaccine to sterilize you or give you cancer, and then they can make more money from the treatments for those things.

They’re already banning many of these vaccines in dozens of countries, but they haven’t even been officially approved yet, won’t finish stage three trials for another couple of years.

Thousands of experts who were previously vaccine designers and makers are being censored for loudly calling for them to stop doing what they’re doing completely. Keep that firmly in your mind if they tell you you’re vaccine hesitant or whatever.

Moderna has partnerships with AstraZeneca, Merck, and The Bill and Melinda Gates Foundation who said if they do a really good job on vaccines and health care, they can reduce the population of the world ten to fifteen percent.

“I would say that mRNA is better suited for diseases where treatment for short duration is sufficiently curative, so the toxicities caused by delivery materials are less likely to occur,” said Katalin Karikó, a pioneer in the field who serves as a vice president at BioNTech.

That makes vaccines the lowest hanging fruit in mRNA, said Franz-Werner Haas, CureVac’s chief corporate officer. “From our point of view, it’s obvious why [Moderna] started there,” he said.


Leave a Reply

Fill in your details below or click an icon to log in: Logo

You are commenting using your account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s

%d bloggers like this: