“I have already written about the currency reset and other features of a technocratic future waiting in the wings. —New levels of visible surveillance, social credit scores, universal guaranteed income, Internet of Things, energy-use quotas, smart cities.

—Events can move in several directions, going forward. In this article, I explore one of those directions.

The occasion is this fake pandemic; the big hammer is the vaccine against the phony COVID.

As Fauci mentioned a couple of months ago, it could be a DNA vaccine—new technology—which means it is really gene therapy. Synthesized genes are injected into the body. They purportedly set up immunity. Actually, they PERMANENTLY alter the genetic makeup of the

recipient.

As you can imagine, this creates the opportunity to put many different genes into humans. To try to invent “new humans.”

The so-called immunity certificates Fauci is now talking about? They would be issued to people who test positive on the new antibody tests for COVID-19—which is an interesting turnaround, because, since 1984, positive tests results have generally been taken to mean “infected.” Why the shift?

Because there is a need for these immunity certificates—as an INTRO to condition the population to an IDEA.

If and when the COVID vaccine arrives, the certificates would be used to signify immunity for all those who take the shot.

It would function as a license. Your passport into the Brave New World. You’re “immune,” so you’re allowed to move out of fear mode. And circulate and travel and enter schools…

For DNA vaccines, the reference is the New York Times, 3/15/15, “Protection Without a Vaccine.” It describes the frontier of research. Here are key quotes that illustrate the use of synthetic genes to “protect against disease,” while changing the genetic makeup of humans. This is not science fiction:

“By delivering synthetic genes into the muscles of the [experimental] monkeys, the scientists are essentially re-engineering the animals to resist disease.”

“’The sky’s the limit,’ said Michael Farzan, an immunologist at Scripps and lead author of the new study.”

“The first human trial based on this strategy — called immunoprophylaxis by gene transfer, or I.G.T. — is underway, and several new ones are planned.” [That was five years ago.]

“I.G.T. is altogether different from traditional vaccination. It is instead a form of gene therapy. Scientists isolate the genes that produce powerful antibodies against certain diseases and then synthesize artificial versions. The genes are placed into viruses and injected into human tissue, usually muscle.”

Here is the punchline: “The viruses invade human cells with their DNA payloads, and the synthetic gene is incorporated into the recipient’s own DNA. If all goes well, the new genes instruct the cells to begin manufacturing powerful antibodies.”

Read that again: “the synthetic gene is incorporated into the recipient’s own DNA.”

Alteration of the human genetic makeup.

Not just a “visit.” Permanent residence.

The Times article taps Dr. David Baltimore for an opinion:

“Still, Dr. Baltimore says that he envisions that some people might be leery of a vaccination strategy that means altering their own DNA, even if it prevents a potentially fatal disease.”

Yes, some people might be leery. If they have two or three working brain cells.

This is genetic roulette with a loaded gun.

And the further implications are clear. Vaccines can be used as a cover for the injections of any and all genes, whose actual purpose is unannounced.

The vaccine masters have a problem. They know their genetic technology is far from perfect. Plans to re-engineer the human race are not a simple one two three.

For example, consider the latest and greatest genetic tool, called CRISPR.

Here is a backgrounder I wrote a year ago.

New CRISPR gene-editing: the extreme dangers

Technologynetworks.com (6/26/17): “CRISPR gene editing is taking biomedical research by storm. Providing the ultimate toolbox for genetic manipulation, many new applications for this technology are now being investigated and established. CRISPR systems are already delivering superior genetic models for fundamental disease research, drug screening and therapy development, rapid diagnostics, in vivo editing and correction of heritable conditions and now the first human CRISPR clinical trials.”

All hail.

It’s called CRISPR, a much faster, more precise, and cheaper technique for editing genes. Researchers are in love with it. You can find hundreds of articles and studies fawning over the innovation.

At phys.org, however, we have this, ahem, warning note (5/29/17): “…a new study published in Nature Methods has found that the gene-editing technology can introduce hundreds of unintended mutations into the genome.”

Oops.

“In the new study, the researchers sequenced the entire genome of mice that had undergone CRISPR gene editing in the team’s previous study and looked for all mutations, including those that only altered a single nucleotide.”

“The researchers determined that CRISPR had successfully corrected a gene that causes blindness, but Kellie Schaefer, a PhD student in the lab of Vinit Mahajan, MD, PhD, associate professor of ophthalmology at Stanford University, and co-author of the study, found that the genomes of two independent gene therapy recipients [mice] HAD SUSTAINED MORE THAN 1500 SINGLE-NUCLEOTIDE MUTATIONS AND MORE THAN 100 LARGER [GENE] DELETIONS AND INSERTIONS. None of these DNA mutations were predicted by computer algorithms that are widely used by researchers to look for off-target effects.” (Emphasis is mine.)

“’Researchers who aren’t using whole genome sequencing to find off-target effects may be missing potentially important mutations,’ Dr. Tsang says. ‘Even a single nucleotide change can have a huge impact’.”

Genetic roulette is alive and well.

Spin the wheel, see what numbers come up. Good effects, bad effects, who knows? Step right up and take your chances.

Of course, researchers who admit these tremendous problems remain optimistic. They look forward to “refining the method.” That’s a cover for: “we really don’t know what we’re doing right now.”

Unfortunately, much science operates in this fashion. Launch a new technology, and turn a blind eye to the consequences. For example, place mercury, a devastating neurotoxin, in vaccines. What harm could result—aside from the destruction of children’s brains.

Here is more gushing PR, otherwise known as throwing stuff at the wall and seeing what sticks: “There are weekly press releases and updates on new advances [in CRISPR] and discoveries made possible with this technology; the first evidence is now emerging that CRISPR-Cas9 could provide cures for major diseases including cancers and devastating human viruses such as HIV-1.” (technologynetworks.com)

The train has left the station.

And just in case you think only the most careful and competent leading lights of the genetic research community would be permitted to get within a mile of CRISPR, here is more from technologynetworks.com:

“CRISPR-Cas9 systems, tools and basic methodology are very accessible as ready to go toolkits that anyone with lab space and an idea can pick up and start working with…In response to a growing need, companies such as Desktop Genetics have developed open access software to accelerate CRISPR experimentation and analysis.”

That’s good to know. “Anyone with lab space and an idea” can jump on board and have at it.

Do your own cross breeding of the pregnant phrases, “What could possibly go wrong,” and “Nothing to see here, move along,” and you’ve summarized the situation.

“They say they cured my anemia, but now I turn green and purple and I keep falling down.”

If all this isn’t enough to make you see the dangers of CRISPR, consider this statement about engineering human immune cells (T-cells) in a “safer” way. From statnews.com (June 23, 2013):

“The experiment would alter the immune system’s T cells only after they’re removed from a patient. That gives scientists the chance to screen the CRISPR’d cells to make sure only the three intended genes, all involved in making T cells find and destroy tumor cells, are altered. But after those T cells are infused back into a patient to fight melanoma, sarcoma, or myeloma, the CRISPR system can keep editing DNA, and tracking such edits becomes like following a polar bear in a snowstorm.”

Not very comforting. Once set in motion, even under the most protected and limited conditions, CRISPR can keep on working, scrambling genes in unknown ways.

So…when it comes to DNA vaccines, aka gene therapy, a plan to precisely re-engineer humans could quite easily descend into uncontrolled chaos.

And the controllers and elite funders of the vaccine know that.

What to do?

With the global population as their guinea pigs, perhaps they would start small. Introduce the slightest possible gene-alteration, stand back and see what happens. Try out a gene that would ordinarily—hopefully—achieve next to nothing. Try to measure the results.

Viewed from one angle, the whole fake epidemic is a set-up for the vaccine, and for mandatory vaccines.

I have written about the special exemption from liability recently issued by the US Dept. of Health and Human Services. Basically, anyone associated with pharmaceutical strategies undertaken “against the coronavirus” cannot be sued, regardless of “adverse effects” of medicines or vaccines.

Taking a stand against mandatory vaccines—any and all vaccines—is more important than ever.