A Possible Cause Of FOGVID Is Zwitterionic Polymers

It may be that Bill Gates’ mosquitoes aren’t the only involuntary vaccine vector being illegally tested upon the American public.

Americans alarmed by ‘chemical fog’ spreading across the US: Phenomenon sparks bioweapon conspiracy theories after drone sightings

h ttps://www.msn.com/en-us/weather/topstories/americans-alarmed-by-chemical-fog-spreading-across-the-us-phenomenon-sparks-bioweapon-conspiracy-theories-after-drone-sightings/ar-AA1wXHkJ

By Brooke Kato for Washington Post, 4 January 2025

New year, new conspiracy theories.

It’s true, then! The denial came so fast, I don’t even know what we’re talking about yet!

Parts of the US have been blanketed by a “mysterious” fog, sparking concern from locals who claim it has a “chemical” smell and exposure can result in flu-like symptoms.

A Florida resident told the Daily Mail that they felt sick after being outside in the fog for just 10 minutes.

“Within about an hour, I kept sneezing over and over for about three hours, and my eyes were really puffy,” the unnamed Floridian claimed. “I got very warm and I felt like I had a fever, and my stomach was cramping.”

The Daily Mail reports that the occurrences have eerie echoes of “Operation Sea-Spray” — a secret biological warfare experiment conducted by the US Navy back in 1950.

At the time, serratia marcescens and bacillus globigii bacteria were sprayed over the San Francisco Bay area to determine how vulnerable a large American city may be to a bioweapon attack. At least one American was killed and 10 others were seriously sickened.

How many military officers and ((civilian advisors)) were publicly hanged for that bioweapon deployment? Zero.

And here we are today, with people expressing zero trust in their leadership, specifically on the topic of bioweapon deployment.

Conspiracy theories have run rampant on social media as people in multiple states have reported a similar phenomenon, which comes after drone sightings in some areas of the country.

Footage online shows a flurry of particles floating within the fog, sparking fears that it is no ordinary weather event but rather, some sort of bio-weapon, users allege.

“Described as a thick, lingering blanket, the fog has left people sick—many experiencing sudden cold or flu-like symptoms after only brief exposure,” one person explained on X of the “so-called ‘chemical fogs’.” “Dubbed ‘Fogvid-24,’ some victims have also reported an unexplained loss of energy.”

According to The Daily Mail, people on X have reported “strange smells” that burn their noses, speculating that the government “dumped a bunch of microbes on the country this week, in the form of fog.”

“It tastes and smells like after setting off a lot of fireworks. That sulfur smell,” one TikTok user wrote, adding that it is “freaking me out.”

Meanwhile, a Kansas resident also told the outlet that she saw “massive amounts of chemtrails” in her area preceding the onset of the fog.

However, there is a scientific reason for why fog forms — and it has nothing to do with biological weapons.

Fog, a cloud of water droplets or ice crystals that form close to the earth’s surface…

Ohhh, fog is just water vapor! “And if the water vapor burns your eyes and stinks of sulfur, well, then maybe it has a few contaminants. Don’t worry about it.”

No, modern America is not London at the height of its coal usage. I looked for alternative, less Narrative-approved explanations, lying on this side of 1950… and I knew where to look.

Delivering the Promise of Gene Therapy

h ttps://inside.battelle.org/blog-details/delivering-the-promise-of-gene-therapy

By Andrea McCue, 21 August 2023

If you’re just joining us, Battelle Memorial Institute is the Freemasonic umbrella corporation that operates ALL of the United States’ research centers that aren’t university-affiliated. You might know them by names such as Sandia National Labs, or Lawrence Livermore, or…

CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) was discovered in 1993 as a naturally occurring acquired immune system in bacteria, for the protection against invading viral DNA. In the decade that followed, interest in this very bacteria-centric field of study grew, as researchers propelled the initial discovery of CRISPR from obscure biological research to advanced study.

Huh, those machines are based on a bacterium’s immune system?

In 2013, the CRISPR system was reconstituted in a test tube with its minimal necessary components, laying the foundation for a universally programable gene editor. Later that year, researchers used CRISPR for the first time in mammalian cells, demonstrating the ability to edit genomes in a completely different kingdom of life.

The decade since has brought not only a Nobel Prize1 for this discovery but also a deluge of CRISPR literature. Researchers in diverse communities around the world quickly adopted this technology, editing the genomes in organisms across the tree of life.

Continued modification has led to ongoing development and innovation, resulting in an array of powerful and precise CRISPR-based gene editors.

Most importantly, the last decade has brought CRISPR to the cusp of human gene therapy. In 2021, clinical trials conducted by both Editas and Intellia treated the very first groups of humans with CRISPR-based therapies.

That’s a guarantee of the Apocalypse, not a sign. I know we’re going into the End Times, because if God does not interrupt this DNA-tampering technology development then humanity is unquestionably doomed. They’ll mutilate our children before they’re even conceived.

Either God is about to nuke the entire planet to pre-microchip tech, and somehow keep us there, or He doesn’t care if the children of Satan contaminate the very DNA definition of God’s Greatest Creation In His Image. The latter will be true when, and only when, humanity’s remaining time is shorter than a generation.

I bet those plagues of John’s Revelation… contamination of the freshwater supply, blotting out the sun, open sores on everybody… will, like Hollywood movies, turn out to be inspired by real-life events.

In June of 2023, the FDA accepted a biologics license application (BLA) for Exa-cel,2 a CRISPR-based cell therapy to treat sickle cell disease and transfusion-dependent β-thalassemia (TDT), putting the field on track to see the first FDA approved CRISPR based therapy by 2024.

As they say, the future is now. BUT, the future has a problem!

Despite these breakthroughs, the next era of gene therapy hinges on the precise delivery of the genetic payloads to their target cells or tissues.

Simply put, a viable delivery solution needs to protect the target, bind to a precise cell, cross the cell membrane, and release the cargo.

Traditionally, these payloads are administered via viral delivery methods, but several drawbacks are stunting progress.

Time and Expense

Viral delivery vehicles are difficult to mass produce, with problems including low purity and yield, resulting in expensive and inefficient manufacturing.

Low Cargo Capacity

Next-generation CRISPR therapies (such as base and prime editors) are too large to be encapsulated in a singular viral genome.

Prolonged Expression

Once genetic modifications are made, viral genomes can persist for years in the nuclei of their target cells. Over time, this continued expression can lead to off-target effects and unintended alterations.

Unintended Immunity

The body can acquire immunity to therapies in cases where multiple doses are required.

Immunogenicity

The immunogenicity of viruses may cause hepatotoxicity at doses required for effective gene therapy.

A New Method of Delivery

Polymeric nanoparticles (PNP) show major promise as a non-viral delivery method for gene therapy. PNPs could be the key to the safe and efficient delivery of a diverse range of therapeutics.

Although tiny, the nanoparticles can carry a larger payload than viral vectors. The diversity provides the potential to identify PNPs that target specific cell types, reducing unintended impacts of off-target delivery. PNPs also make repeat application possible, avoiding immunogenicity. Finally, once the intended cells are modified, the gene editing machinery naturally degrades.

Researchers at Battelle are taking PNPs one step further. They have designed a robust synthesis platform with tracking and machine learning capabilities to unlock high-throughput in vitro and in vivo screening of up to one thousand nanoparticles at a time.

They probably designed that with data from their COVID-nanoparticle science experiment.

h ttps://gunnerq3.substack.com/p/why-darpabattelle-put-graphene-in

So, obvious question: if viral delivery methods are becoming obsolete for the above-stated reasons, then is inhalation of nanoparticles one of the alternatives being considered?

No More Needles? Inhalable mRNA Could Revolutionize Medicine

h ttps://scitechdaily.com/no-more-needles-inhalable-mrna-could-revolutionize-medicine/

By the American Chemical Society, 13 November 2024

Dated just two months ago.

A groundbreaking study introduces stable inhalable mRNA treatment using nanoparticles that hold up during nebulization, showing significant potential in treating lung diseases without injections.

Many people dislike getting shots for treatments or vaccines…

They don’t trust the science!

…so scientists are exploring ways to develop medicines, like those made from messenger RNA (mRNA), that can be inhaled instead. A new study published today (November 13) in the Journal of the American Chemical Society highlights key progress toward creating inhalable mRNA therapies. Researchers describe their advanced lipid-polymer nanoparticle that can hold mRNA in a stable form for nebulization and deliver it effectively as aerosol droplets to the lungs of mice.

mRNA medicines work by encoding proteins that could help treat or prevent various diseases, including those affecting the lungs. However, these proteins are fragile and cannot penetrate cells on their own. To protect and deliver mRNA to lung cells, scientists use lipid nanoparticles—tiny fatty spheres that act like “suitcases,” carrying the mRNA safely to its target.

Yet, early versions of these lipid nanoparticles were unsuitable for inhalable treatments, as they tended to clump together or expand in size when sprayed. Previous efforts to solve this issue involved adding polymers, like polyethylene glycol, to the lipid particles. However, this approach did not provide sufficient stability for effective nebulized delivery.

Innovative Solution With Zwitterionic Polymers

Now, Daniel Anderson, Allen Jiang, Sushil Lathwal, and colleagues have hypothesized that a different type of polymer, one with repeating units of positively and negatively charged components called a zwitterionic polymer, could create mRNA-containing lipid nanoparticles that can withstand nebulization (turning a liquid into a mist).

Then in animal trials, the researchers determined that a lower-cholesterol version of the lipid nanoparticles with zwitterionic polymers was the optimal formulation for aerosol delivery. When transporting an mRNA encoding a luminescent protein, this nanoparticle produced the highest luminescence within the animals’ lungs and a uniform protein expression in the tissues, thereby demonstrating that it had the best ability to deliver inhaled mRNA.

Mice given three airborne doses of the optimal nanoparticle over a 2-week period maintained consistent luminescent protein production without experiencing measurable inflammation in the lungs. The delivery method even worked in mice with a thick layer of mucus lining their airways, which was meant to model the lungs of people with cystic fibrosis.

Taken together, the researchers say this set of results demonstrates the successful airborne delivery of mRNA using zwitterionic polymers in lipid nanoparticles. As a next step, they plan to conduct tests in larger animals.

Larger animals, they say.

Two months later, humans are complaining about dispersed particles in mist irritating their eyes and lungs.

I don’t know that it’s the field-testing of Zwitterionic PNP technology, but the explanation and timeline fit very well.

A way to test this is whether luminescent proteins begin showing up in peoples’ lungs, like those lab mice, or maybe those quantum-dot identifiers that Bill Gates invented. It would be something that a camera or flying drone would be able to detect, because a Man In Black ringing your doorbell to check your pulmonary function “for no reason at all” would be awkward.

Or, maybe they’re delivering a flu vaccine for an engineered flu they’re waiting to spray on those same populations in another few weeks. It IS almost flu season, isn’t it? and the newest flu vaccines are mRNA-based.

Postscript

I found this article while researching how mRNA contaminants are being spread into reproducing animals. It’s worth posting on its own.

Genetically Modified Chickens Don't Pass On The Flu

h ttps://www.npr.org/sections/health-shots/2011/01/19/133027476/genetically-modified-chickens-dont-pass-on-the-flu

By Richard Knox, 19 January 2011

Here's a neat genetic trick: Make a chicken that can get the flu, but can't pass it on to other birds -- or, presumably, to the humans who take care of them.

Playing God is a bad idea.

British researchers have done it.

Sigh.

The British team, with the support of a big poultry breeder and government funding, inserted a gene into chickens that blocks flu viruses from replicating. These genetically modified chickens can get infected. But their cells don't spew forth zillions of copies of flu viruses -- so nearby poultry don't get sick.

We’ve heard that one before. Other articles confirmed that the gene turns chickens into superspreaders who don’t become symptomatic. An artificial Marek’s Disease situation.

Their achievement, reported in the current issue of Science, addresses major problems for both poultry breeders and public health officials who worry about chickens as sources of flu viruses that make humans sick.

If these hurdles can be overcome, it might not be such a daunting task to replace the billions of ordinary chickens in commercial poultry herds with the GM type.

That means food supply. It also means they’d has to mass-cull billions of chickens… like they’re already doing… maybe on a state-by-state basis…

"That's because the trade in both broiler and egg-laying chickens has become consolidated in a handful of companies," Michael Greger of the Humane Society of the United States told Martin Enserink of Science.

They were passing this idea around… permanently mutating chickens to spread a plague faster than it normally would… back in 2011? a decade before COVID?