Graphene meets RNA technology, for cancer vaccines

Double trouble

by Jon Rappoport

July 13, 2021

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As soon as Operation Warp Speed was announced, I made it clear that one of the prime goals was: winning approval for experimental RNA technology.

RNA tech had never gotten a green light prior to the COVID vaccine. Why? Because it was highly dangerous. Generally speaking, massive inflammatory response was the issue: the body attacks itself.

But RNA tech allows new vaccines to be developed faster, easier, and cheaper. Therefore, researchers could claim to discover new viruses at the drop of a hat (without authentic proof), and pharma companies could develop new vaccines (aka genetic RNA treatments) overnight.

It became Bill Gates’ and Tony Fauci’s mission to drag an RNA COVID vaccine across the finish line to emergency-use approval, come hell or high water. They were determined to crack open the marketplace for a flood of RNA medical products.

In yesterday’s, article, I highlighted the arrival of a “miracle” substance, graphene, trumpeted as the core of a whole new frontier in medicine.

For example, Merck is using it to research the creation of IMPOSED nerve responses in the body, in order to knock out a whole host of “disease conditions.”

Of course, the acknowledged toxicity of graphene nanoparticles is underplayed; in particular, their tendency to cause lung infections.

And now graphene and RNA tech meet, in new research into cancer vaccines. As they say, what could possible go wrong?

The reference is “In Situ Transforming RNA Nanovaccines from Polyethylenimine Functionalized Graphene Oxide Hydrogel for Durable Cancer Immunotherapy,” 2/17/21, ACS Publications.

Here is an excerpt from the optimistic abstract: “Messenger RNA (mRNA) vaccine is a promising candidate in cancer immunotherapy…Here, we report an injectable hydrogel formed with graphene oxide (GO) and polyethylenimine (PEI). The released nanovaccines can protect the mRNA from degradation and confer targeted delivering capacity to lymph nodes…”

The scramble is now underway to deploy both RNA genetic tech and graphene in all sorts of medical “innovations.”

You don’t get just one danger; you get two.

And here is a third wrinkle. According to conventional vaccine theory, the injected RNA would cause cells of the body to produce a protein unique to cancer tumors. The immune system would attack this protein and, up the road, be prepared to destroy cancer before it could gain a foothold.

It’s possible that researchers from the old failed US viral cancer project of the 1960s and 70s could now rewrite history, get in line, and say, “We never failed. Robert Gallo DID discover two cancer viruses, which also have unique proteins. Let’s develop an RNA-graphene injection that empowers the immune system to attack these viruses…”

I mention this because those failed cancer researchers went on to claim a new virus called HIV caused a condition called AIDS. And like COVID, the “causative virus” was never isolated, never proved to exist.

HIV and SARS-CoV-2 are both phantom fantasies. And in both cases, the drug/vaccine treatments are massively destructive.

The medical cartel at work.

The Matrix Revealed

(To read about Jon’s mega-collection, The Matrix Revealed, click here.)

Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

Genetic baloney in thick slices

by Jon Rappoport

July 8, 2021

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Gene research companies tend to come and go. They start out banging and popping like fireworks in the sky, and then they fade out—selling themselves to larger outfits who’ve hired better liars…

Once upon a time, it sounded easy. Start with a disease, find the gene responsible for the disease, and correct the problem.

Then, researchers wondered, was disease the result of one gene or a group of genes acting together?

Either way, the proof would be in devising cures for diseases using gene therapy. “Not yet, but soon…”

And regardless, the major need was: money. Lots and lots of money.

This need required good PR people. “We have to pump up the idea that we’re on the edge of tremendous breakthroughs. We’re always on that edge…”

This hype also needed to obscure the fact that there wasn’t (and isn’t) ANY gene cure for ANY disease.

As time passed, lack of cure could be a problem. In fact, it could mean curing disease was not a genetic undertaking at all. What about environment? Toxicity? Malnutrition? Poverty? In order to raise money, those factors would have to be pushed back out of view.

Instead, the PR people would need to flood the news with positive glow around the subject of gene research. Also known as exaggeration. Or bullshit.

You can spot the key terms in these articles. POSSIBLE, SHOULD, COULD, EXPECTED TO, SEEMS, ON THE HORIZON, MAY BE, COULD LEAD TO, EVENTUALLY, and of course, the ever-popular BREAKTHROUGH.

I dug back in my files and found a piece I wrote in 2011. As you’ll see, the “breakthroughs” touted then haven’t panned out so far. You don’t read about them in the press these days. The PR pros have moved on to other exaggerations.

The first 2011 article I cited was from Reuters, headlined: SCIENTISTS FIND “MASTER SWITCH” GENE FOR OBESITY. Here are a few choice tidbits. Note the key terms I just mentioned.

“…and say it should help the search for treatments…”

“…the regulating gene could be [a] target for drugs to treat…”

“…seems to act as a master switch…”

“We are working hard…to understand these processes and how we can use this information to improve treatment…”

Sure. You bet.

Zero results.

Next, a 2011 blockbuster piece in the Financial Times. The headline read: SCIENTISTS FIND GENETIC LINK TO DEPRESSION.

Standard trumpet blaring.

Here are the text nuggets. Again, note key terms.

“The discovery…is expected to lead to a better biological understanding of the condition and eventually to more effective antidepressants…”

“…as possibly for the first time we have found a genetic locus for depression.”

“…is likely to pin down the gene responsible…”

“…which may be the basis for designing more effective antidepressants…”

Sure. You bet.

Zero results.

Moving ahead in time—From “On 17 December 2015, the journal Science voted [gene-editing tool] Crispr-Cas9 ‘Breakthrough of the Year’, saying that it had ‘matured into a molecular marvel’. It is already being used in cancer immunotherapy to edit a patient’s own T-cell genome in order to remove the gene that ‘tells’ these immune cells not to target cancerous tissue.

It’s already being used—but where are the cures? Nowhere.

Anybody out there want to partner with me in launching a new company? This is a major winner. It covers a very broad area. Actually, there is no human endeavor it doesn’t cover. The name of the company? MAYBE COULD BE INC.

“We’re always on the edge and the frontier. We’re always breaking through. We’re always raising money. We’re always pumping our stock. We’re always ready to sell the company to a sucker with deep pockets.”

Let’s look at another type of gene research organization. This one happens to be the largest single medical research outfit in the world. It’s part of the US government: the National Institutes of Health (NIH). Their PR is different. They’re hedging their bets and covering their bases in every possible way. They’re saying YES, NO, AND MAYBE all at once. Of course, they can get away with it, because they run on taxpayer money. Their annual budget is a formidable $30 billion. Grit your teeth and read through their text that explains “genetic diseases”:

“A genetic disorder is a disease caused in whole or in part by a change in the DNA sequence away from the normal sequence. Genetic disorders can be caused by a mutation in one gene (monogenic disorder), by mutations in multiple genes (multifactorial inheritance disorder), by a combination of gene mutations and environmental factors, or by damage to chromosomes (changes in the number or structure of entire chromosomes, the structures that carry genes).”

“As we unlock the secrets of the human genome (the complete set of human genes), we are learning that nearly all diseases have a genetic component. Some diseases are caused by mutations that are inherited from the parents and are present in an individual at birth, like sickle cell disease. Other diseases are caused by acquired mutations in a gene or group of genes that occur during a person’s life. Such mutations are not inherited from a parent, but occur either randomly or due to some environmental exposure (such as cigarette smoke). These include many cancers, as well as some forms of neurofibromatosis.”

That is a DON’T BLAME US statement. “Don’t blame us if a disease we thought was genetic turns out to be something else. Don’t blame us if it’s 65.34 percent environmental, 4.52 percent genetic, and 30.14 percent who knows what. Don’t blame us if toxicity triggers genetic malfunctions and, in the absence of the toxicity, there would be zero cases of the disease. Don’t blame us if a disease has nothing to do with genes. We’re ready to jump in any direction. We may not know much, but we’re sitting on a pile of cash. Don’t blame us if we don’t have any solid genetic cures for anything. We’re working hard. That’s all you can ask us to do.”

If there is one disease the public tends to believe can be cured by gene therapy, it is sickle cell anemia. The PR pros have done a good job there. However, states: “Gene therapy is an experimental technique that aims to treat genetic diseases by altering a disease-causing gene or introducing a healthy copy of a mutated gene to the body.”

Experimental. Aims to. Not an established cure. The confusion arises because, as with a number of diseases, the researchers and the PR flacks claim they’ve definitely traced the illness to a gene or two. They’ve struck gold. But, as you read further, you discover they’re just not ready to cure the patient. Clinical trials are underway. More work in the lab is necessary. The pudding is there, but the proof of it isn’t. They claim to know the cause; they just don’t know what to do with it.

In science, that’s known as a hypothesis. Or more simply, a speculation. You say you’ve found an answer, but you can’t apply it. This means: you don’t have an answer.

“There is no doubt. We went down into the mine and we found evidence of extraordinary amounts of gold. We just don’t know how to get it out. What’s that? You want to see the gold? No, I’m sorry. The public isn’t allowed down there. Only the professionals can enter. But don’t worry. We’re very close to a breakthrough. The gold will emerge soon. Trust us.”

Trust you? Sure. How much do you need to finish the job? Fifty million? A hundred million? Let me call my broker and sell some stock. I’ll write you a check. Just put a plaque with my name on the wall. Let me know how I’ll profit on this venture. I’m in. I’ve always wanted to invest in MAYBE COULD BE INC.

In case you need to be reminded, the RNA COVID vaccines are genetic treatments. The PR pros tell us they are working quite well. And they’re remarkably safe.

If you’re buying that line, I have electric cars for sale. And they have wings. One charge in your garage, and they’ll get you from Earth to Mars in just under two hours.

The Matrix Revealed

(To read about Jon’s mega-collection, The Matrix Revealed, click here.)

Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

COVID-19 is a plague spreading death across the country and globe… Or is it?

Terran note: This is the second essay I received without a name on COVID vaccines.

COVID-19 is a plague spreading death across the country and globe… Or is it?

Let us first assess the concept of infection used to promote the COVID-19 pandemic. Daily, in every form of media, we are told that millions of people are being “infected” with COVID-19. Yet the definition of infection with COVID-19 virus is principally testing positive for the virus using a nasal swab test. However, the presence of germs-like COVID-19-in our nose is not a demonstration of an infection.

A rich mixture of microorganisms reside on our skin, in our mouths, ear canals, our intestines, and yes, in our noses. The skin, mouth, and nose are fundamentally purposed to provide barriers to germs- so that we dont get infections. Germs harmlessly colonize these areas. The germs on or even in our bodies such as the nasal passages- are colonizers, and their presence is not ever considered to represent an infection. Indeed, if all the germs isolated from a single nasal swab from one healthy individual were identified, any assortment of the following might be present: Staphylococcus aureus (S. aureus), Streptococcus pneumoniae, Haemophilus influenzae, Propionibacterium acnes, rhinovirus, respiratory syncytial virus, infuenza A, Influenza B, rotavirus, Epstein barr virus and yes, the coronavirus and even the COVID- 19 variant (to name a few).

If we considered every germ in the nose an infection-like we do for COVID-19–the outcome would be absurd. For example, about 20% of people have nasal colonies of the potentially lethal bacteria S. aureus. If over the next year we nasal swabbed every nose in the United States for S. aureus, and we accepted nasal colonies to represent infection, about 66 million people would be considered “infected” by the bacteria. Hospitals and clinics would be flooded with S. aureus “infected patients and the greatest outlay of antibiotics and “vaccinations” in the history of the world would ensue. In addition, of the 2.8 million deaths expected in the US over the next year, 20%, or 560,000 deaths could be considered S. aureus associated. If the US government were paying hospitals to list this as cause of death on death certificates as they are now with COVID, S. aureus would be a new leading cause of death in the US.

Like a parlor trick, the immunological assessment normally used to test for an acute infection (serological testing for IgG/lgM antibodies) was cast aside for this pandemic, and an irrelevant but wildly positive nasal swab testing approach was used to build fear of a COVID-19 outbreak. The nasal swab has not actually provided a shred of evidence that there is an outbreak of clinical infections with COVID-19 virus.

Since there is no evidence of an outbreak of COVID-19 infections, we might ask does epidemiology data-ie. the appearance of unexpected infectious disease-related deaths in the community-support the notion that we are in the midst of pandemic?

Interestingly, the availability of transparent epidemiological data in the US and other countries is difficult to find right now. One exception is the fairly comprehensive datapublished in Canada by the British Columbia Center for Disease Control (BCCDC) 1. BC is the third most populous province (5.1 million) in Canada and the BCCDC is the official source for data relating to what it considers to be COVID-19 related morbidity and mortality. The BCCDC transparency includes acknowledging its mortality data for individuals who did not test positive for COVID-19 but were considered to be infected by COVID-19 based purely on symptoms and/or likely exposure to someone that may have been COVID-19 infected. Based on this broad definition of COVID-19 infection, from January 15 through November 21, 2020 the BCCDC reported a total of 354 deaths in BC were associated with COVID-19 “infection”. Among the 354 deaths, 69% were individuals over 80 years old, and 35% of the deaths occurred with people over 90
years old. The median age at death overall was 85 years. Over the course of a year,

354 persons with a median age of 85 in a population of 5.1 million people died-this is a pandemic? Let’s have a closer look.

Consider the background mortality rate for the age group: based on historical actuarial data, 10% of persons 85 years old will die before their 86th birthday. Therefore, in British Colombia there are over 200,000 individuals over 85 years old and thus we could have expected about 20,000 deaths in the same demographic as those reported to have died from COVID-19 associated ilness. Only 354 deaths were attributed to COVID-19 among the 20,000-background mortality. Not too convincing for the greatest pandemic of all time- and hardly justification for collapsing commerce, immigration, and emigration, as well as limiting all forms of social interactions.

In the United States, epidemiological support for a pandemic is similarly difficult to grasp. During the past year, the US could have expected about 1.3 million deaths for the 80+ year-old population, the main demographic for COVID-19-associated deaths. During 2020 it was claimed that 400,000 elderly deaths in the US were COVID-19- associated. If these 400,000 deaths were in addition to the 1.3 milion expected, it would mean the size of the COVID-19 population susceptible to death from the virus (the 80+ year-old population) would be shrinking and thus over time the mortality rate should either be decreasing, or the population dying from the virus should be shifting to a younger age group because fewer remain in the 80+ population. Neither of these is occurring. To the contrary, the 7-day average for deaths related to COVID-19 as reported on December 31, 2020 was 3,462; on April 17, 2020, the height of the “pandemic,” there was a weekly average death rate reported of only 2,232. The death rate among the elderly population is repotedly increasing. If the 400,000 elderly deaths were in addition to what was normally expected among this population, the population would be declining and so would the number of deaths. There is no evidence the population over 80 years old has declined or is declining; and this tells us that there is no excess mortality occurring in that population. There can be only one explanation: that the 80+ year-old population said to be succumbing to COVID-19 are actually dying at an expected and normal rate, and thus there is no COVID-19-related excess mortality in the over 80 age group.

1 British Columbia (BC) COVID-19 Situation ReportWeek 50: December 6-December 12, 2020.

Then who is dying – what are the details of the so-called COVID-19-related deaths? Patients with terminal illnesses who would have been directed to hospice and extended care facilities are now being given COVID-19 diagnoses (ie., in some cases due to nasal swabs; in other cases it’s just assumed). They are shunted into hospitals, which receive money from the government for each COVID-19 admitted patient, and there they often receive unnecessary but profitable treatments for the hospital, their quality of life is decreased, they are kept from seeing family and friends, and many die alone and in pain. Feeble elderly, cancer patients, and stroke victims have been taken from extended care facilites and brought to die (for a proft) in hospitals. Samira Beckwith, president and CEO of Hope Healthcare, a large nonprofít hospice program in Fort Myers, Florida, summed up the situation in a revealing remark: “I just wonder, where are the people who should be coming to hospice with all the usual diagnoses, such as cancer?”2 It is worth consideration to question why the hospice industry seems to be suffering from a lack of business during the COVID-19 pandemic.

Based on COVID-19 testing strategies, there is no evidence that an infectious outbreak has occurred; and epidemiological findings simply provide no evidence of a significant increase in mortality among any demographic, not even those with a median age of 85 years who are naturally vulnerable to infectious disease.

Nevertheless, to rescue the population from the scourge of COVID-19, the largest and most costly effort ever to develop a vaccine was launched with unprecedented financial and political support of government, Fauci, and the Gates foundation. Strangely, the vaccines championed for development didn’t rely on any of the proven approaches, those that have been used in vaccine development for the past 70 years. Rather, government agencies, ostensibly racing to save the world from a deadly pandemic, inexplicably opted to support not only unproven, but historically ineffective vaccine strategies hyped by two similar start-up biotech companies.

But just how far off from the tried-and-true vaccine approaches were the vaccines the FDA and the federal government raced to support? The government mobilized all its resources behind a highly speculative start-up company — massively promoted on the stock market — to make RNA-based vaccines. The fact is that there is no rational basis for making a vaccine out of RNA and there is no history of such a vaccine ever being used successfully in humans. To the contrary, using RNA as an immunogen (a substance that stimulates the production of antibodies), might be the most counterintuitive and least likely approach conceivable for a vaccine.

2 Hospices Now Ready to Accommodate Coronavirus Patients During Pandemic. (Dying at home with COVID-19 should be an option.) larry Beresford, AARP, May 18, 2020.

Vaccines are primarily designed to stimulate the body’s production of antibodies. Antibodies are substances produced by cells of the immune system that bind and neutralize germs and rid the body of infection. To target the COVD-19 virus, it isessential to stimulate the immune system to generate antibodies that bind to a very specific protein present on the surface of the virus, known as the “spike” protein, which allows the virus to attach to and enter cells in the body.

The immune system must interact with the spike protein and do so in specialized organs of the body (ie. lymph nodes) in order to generate antibodies. When proteins on the surface of a virus- like the spike protein-are recognized by cells of the immune system, this stimulates immune cells to produce excess amounts of antibodies against the virus protein. A vaccine is designed to provide the protein to the immune system in a manner that resenbles what would occur when the same protein is present on the virus. To target the spike protein of the COVID-19 virus, the most straightforward and effective way would be to inject purified spike protein mixed and attached to tiny particles of an inert substance known as alum. This approach, discovered in 1926, is a method of making a so-called subunit vaccine- -meaning a subunit of the virus was used instead of a whole virus in the vaccine. When mixed with the spike protein, the tiny alum particles would help the spike protein get delivered into the lymph nodes, stimulate the immune system to actively react to the protein, and present tiny particles with spike protein on the surface in a way similar to a virus. For nearly a century this approach was the only type of subunit vaccine shown to be safe and effective, and the only approved method in the US for human vaccination. 3

RNA vaccines are nothing like the familiar subunit vaccine: RNA is not a protein, so it cannot directly stimulate an antibody response against the virus spike protein. Instead, RNA is used to indirectly code for the viral protein. To produce the spike protein, the RNA must somehow find its way into cells of the body and instruct the cells to make the protein it encodes. No one knows exactly how the RNA gets into cells, or how it gets to a place in the cells where it can direct them to make the protein. RNA vaccines are known to be extremely inefficient and ineffective. Once the RNA gets into a cell, if the cell produces the desired protein (in this case the spike protein), then the protein must also somehow get presented to antibody-producing cells of the immune system in order to stimulate the production of antibodies against COVID-19.

The likelihood that RNA will get into the proper cells, that it will then trigger production of sufficient spike proteins, and that they will be “seen” by antibody-producing cells is an extremely unlikely event. Therefore, to compensate for the RNA’s being such an inefficient and ineffective immunogen, RNA vaccines are formulated with highly toxic immune stimulants, or adjuvants. More art than science, these adjuvants, in the form of PEG LNPS (pegylated lipid nanoparticles ) are intended to somehow help the RNA get into cells, and to create sucha massive inflammatory response that large numbers of immune cells are recruited to the site of injection. The effect is a local and systemic inflammatory insult that is intended to initiate a very specific antibody response.

3Alum: an old dog with new tricks. Yumei Wen and Yan Shi. Emerg Microbes Infect. 2016 Mar; 5(3): e25.

In addition to being a terible immunogen for a vaccine, RNA might be the worst conceivable substance for a vaccine in terms of its instability and thus its lack of suitability for storage and transport. An adequate storage condition for RNA is around- 112°F. If an RNA preparation warms to even refrigeration temperatures it breaks down into useless debris in minutes.

For the federal government to back the use of risky, unproven and unstable RNA vaccine–intended to address what was ostensibly an existential crisis–defies logic. Conventional vaccines would work to induce antibodies against the spike protein, and are already used for the flu and many other viruses. There have been billions of safe inoculations over 100 years with conventional vaccines. They are simple to make, and very stable to ship and store compared to RNA, So why did the US government finance, faciltate rapid approval, order hundreds of billions of dollars of the RNA vaccine, and now promoting a toxic concoction on US citizens? A look at the timeline of events suggests a frightening collaboration between the US federal government and Moderna (the start-up company behind the first approved RNA vaccine), Fauci, and Gates.

Publicly filed documentation with the Securities and Exchange Commission (SEC) tells an incredible story. On January 13″, 2020, the U.S. National Institutes of Health (NIH) and the National Institute of Allergy and Infectious Diseases (NIAID) had already collaborated with Moderna to design a COVID-19 vaccine, and an agreement was in place to finance the company to launch a COVID-19 vaccine program.4 Incredibly, however, only two weeks earlier had Chinese authorities even announced that there was some kind of unidentified illness in Wuhan! It was not until January 11th: two days before the deal between Moderna and the US govenment that the first COVID-19 genetic sequence was published. The COVID-19 sequence published was derived from a single patient that had experienced and recovered from a respiratory infection.5 It was not even yet known whether this sequence could be related to any of the other infections that were being observed at the time in China.

We are therefore to understand that within two days from the identification of a coronavirus association in a single patient with a respiratory infection in Wuhan, Moderna had already collaborated with the Federal government to design and receive funding for a COVID-19 vaccine program. Federal government officials and Moderna had to know a COVID-19 pandemic was coming; and clearly the profits from the soorn to be pandemic were planned to go Moderna’s way.

It is undeniable that the planning for the pandemic was well underway prior to the identification of the COVID-19 virus on January 114, 2020.

4Moderna’s work on a potential vaccine for COVID-19. Regulatory filings with SEC.

5January 10, 2020 posting of a coronavirus genome relating to a single patient with respiratory infection. Communicated by Edward C. Holmes, University of Sydney on behalf of the consortium led by Professor Yong-Zhen Zhang, Fudan University, Shanghai.
In addition, less than two months prior to that, on October 18″, 2019-ust weeks before the Chinese government would go public with their suspicion that there was an unusual illness circulating in Wuhan province – the Bill & Melinda Gates foundation funded a gathering of world leaders from media, pharmaceutical industry and government to prepare for a coronavirus pandemic. The meeting, billed Event 201, was presented asa “high-level simulation exercise for pandemic preparedness and response6, The intent of the meeting was ostensibly to identify “areas where public/private partnerships will be necessary during the response to a severe pandenic in order to diminish large-scale economic and societal consequences.”

The Event 201 organizers were boldly modeling the pandemic exercise arounda virus they called NCOV, an abbreviation for novel coronavirus. The meeting specifically involved discussion and presentations relating to the social, economic and public relations management of a coronavirus pandemic. At the meeting, media representatives even discussed how to manage dissenting views, and how to quash ideas that challenged government claims of a pandemic. The timing and nature of the discourse impossibly foreshadowed policies and events that only weeks later would be dubbed the novel virus COVID-19″.

Is it reasonably possible that Event 201-planning for the NCOV pandemic – and the launch of the COVID-19 pandemic was simple coincidence? What are the odds? Couple that with the proven fact that both Fauci and Bill Gates are tied to and profiting from patents and the vaccines for this virus, and it is almost impossible to believe that what we are being told is true.

The COVID-19 pandemic generated a crash in the stock markets: February 19h through March 19, 2020, the DOW Jones industrial average lost almost 50% of its value. The overall collapse of the US stock markets represented a swing in value of trilions of dollars. Put another way, for the short-selling hedge fund industry, news of the pandemic provided a payday never before seen in the history of the financial world.

By March 27h, 2020 the US congress approved the largest emergency spending program in history, appropriating $2.700 trilion as part of the CARES Act. At least $1 trillion of these funds remains unaccounted for, including $1/2 trillion the U.S, Treasury Secretary Steven Mnuchin told Congress that he would distribute in secrecy7. Congress is set to announce another multi-trillion-dollar payout as part of a COVID-19 economic strategy-including almost $1/2 trillion to purchase vaccines from Moderna.

By November 2020, the richest 648 individuals in the US were reported to have gained $i trillion in wealth8. Bill Gates, who had the remarkable foresight to organize the nCOV pandemic think tank just weeks before the real pandemic–netted $20 billion himself.

6 Event 201, A Global Pandemic Exercise.

7 Mnuchin Is Keeping $500 Billion In Bailout Funds Secret. Public Citizen, June 11, 2020.

8 U.S. Bilionaires Gained $1 Trillion Since The Pandemic Started. Statista, November 30, 2020. https://www.Statista.Com/Chart/22068/Change-In-Wealth-Of-Billionaires-During-Pandemic/

There is neither infectious disease evidence that a COVID-19 disease is occurring nor epidemiological evidence of an increase in mortality due to any infectious disease cause or any other cause. The launch of an impossibly timed and dangerous vaccine is being thrust upon an unwitting population that has been terrorized into believing in an existential threat from COVÍD-19. When we open our eyes and ears to the facts, the COVID-19 pandemic appears not as a public health catastrophe, but as an event for orchestrating an almost incomprehensible shift in wealth and power, a stripping of freedom that has been globally authorized through fear-and the most extraordinary scam in the history of the world.

Continue reading “COVID-19 is a plague spreading death across the country and globe… Or is it?”

Consciousness Descension into Matter – Lisa Renee and Energetic Synthesis

In Lisa Renee’s latest blog she talks about how our soul consciousness descends into matter from the higher dimensions into our third dimensional physical bodies. This Blog entry is taken from her Ascension Glossary. Just like Wikipedia, highlighted text below is linked to a new title page that gives a detailed description of the linked item.

One would not build a house in our physical world without first creating and then using a detailed blueprint to build off of. Below, Lisa describes how our human physical body has a divine blueprint that works holographically through a 12 Tree Grid template. The architecture is expressed physically through our DNA and RNA.

The Transduction Sequence describes the process by which consciousness undergoes several stages of Descension, passing through multiple layers of dimensionalization in order to manifest into a matter form. Consciousness uses a Blueprint, architecture to express itself in matter. A Core Manifestation Template is designed for consciousness to express itself into the biological form that is located within a specific dimension of time and space. As an example, the original angelic human 12 Strand DNA template is expressed through the holographic template of the 12 Tree Grid, or Kathara manifestation grid. Consciousness units arrange themselves into dimensional grids which form into layers of morphogenetic fields, containing specific instruction sets that build into energy spirals that make up the merkaba fields.

The Merkaba fields are what help to sustain the energy that builds the entire Lightbody construct, in which there are male-female sets of counter-rotating electromagnetic spirals of the consciousness energy. The male-female sets of consciousness energy spirals generate a DNA and RNA imprint. The DNA architecture is the masculine principle, while the RNA is the feminine principle. The DNA-RNA messaging circuitry must communicate together in balance. The DNA and RNA imprint project the entire lightbody hologram which organizes the light of the consciousness into a bio-energetic field, or auric field.

The auric field organizes into multiple layers of energy matrices that act as small computers, and these are the Chakras, the lower exist in the particle layers and the higher dimensional chakras exists in the anti-particle layers. The anti-particle chakras are Morphogenetic Chakras and they inform the instruction sets absorbed into the lower dimensional chakras, who can open the higher contents when they are able to hold the higher frequencies. Over time the chakras dissolve into each other when absorbing the higher dimensional frequencies.

The chakras send their processed energy as intelligent spirals into the nadial capsule which forms around the manifest biological form. The nadial capsule is comprised of the three-dimensional layers of the harmonic universe, in which the consciousness is stationed as an identity. The Nadial Capsule instructs how the consciousness must organize itself into the manifested DNA and RNA cellular biology. The DNA-RNA in matter sends its intelligent design to the Nadial Structure, which acts as the blueprint for energetic transmission and energetic receivers that form into the blueprint for the physical Brain and nervous system. The central nervous system transmits into the molecular structure and then into the nuclear core in the 1D Atomic Body, which informs the Dark Matter Template.

This nuclear core sends intelligent consciousness energy from all combined blueprint layers into the central nervous system, which sets the metabolic and biological base rhythms. These biological base rhythms are imprinted from the Soul and spiritual intelligence into the Blood, which form into the historical spiritual records. This blood record forms an imprint that is recorded in the brain to produce and distribute Hormones, and the natural chemical reactions that are recorded in each organ and gland, and into all cellular tissues.

When we understand the interaction of the consciousness imprints from our Soul and spiritual intelligence recorded into our Blood and biological form, then it becomes obvious that the human body is filled with the personalized spiritual records of that unique consciousness being.

(Source: Ascension Glossary – Consciousness Descension into Matter Biology)