Watch on VideoPress https://videopress.com/v/p8R7ebPy
Please highlight, and copy the above link to share far and wide. Thank you.
Watch on VideoPress https://videopress.com/v/p8R7ebPy
Please highlight, and copy the above link to share far and wide. Thank you.
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. http://www.bccdc.ca/Health-Info-Site/Documents/COVID_sitrep/Week_50_BC_COVID-19_Situation_Report.pdf
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. https://www.aarp.org/caregiving/health/info-2020/hospice-care-coronavirus.html
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 https://cen.acs.org/pharmaceuticals/drug-deliveryWithout-lipid-shells-mRNA-vaccines/99/i8 ) 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.
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. https://www.sec.gov/Archives/edgar/data/1682852/000119312520074857/d884510dex991.htm
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. https://www.centerforhealthsecurity.org/event201/
7 Mnuchin Is Keeping $500 Billion In Bailout Funds Secret. Public Citizen, June 11, 2020. https://web.archive.org/web/20200616172043/https://www.nytimes.com/2020/06/15/Us/Politics/Coronavirus-Ppp-Trump-Congress.Html
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/
The essay below was received with no name attached. I’ve left it as much as possible unaltered. I have corrected spelling and minor grammatical errors (at least the ones I’ve noticed). Comments [in italics and red square brackets] are my own, as is my custom. I am not a doctor, not a molecular biologist, nor do I give medical advice.
I do notice when facts and logic based on scientific papers, don’t match what the Pharma-financed media is saying. Saying “IT’S SCIENCE!” is used to end honest dialog and deplatform concerned science researchers as heretics to the priesthood of Fauci and Collins. In a weird collusion of faith and Pharma, Dr Francis Collins has been the go to evangelist for vaccinations to evangelical America. He shows up at all their conventions. “IT’S SCIENCE!” is not some magic phrase that negates logic and facts makes something based on consensus and repetition of marketing talking points into science. Science at its heart is about disputing assumptions and disproving them.
I’m not even anti-vaccine. There was a time when I had issues with pneumonia, and I haven’t had it since being vaccinated for it. I think some of them do work, they have been time tested. I am not fond of the toxins they use in many of them as adjuvants. Mercury in particular. If I go to a country that requires a yellow fever vaccine I will probably get one. I am, however, not taking an mRNA vaccine for a disease I have already had and survived. I’ve got the antibodies. Everyone must be responsible for their own body. But keep in mind self driving cars don’t have the liability free reign that big Pharma has. That should give you pause.
I am not one that believes these mRNA vaccines will cause a huge number of fatalities. I have come to see over the past 8 years the human body is far more capable of rejuvenation and other astounding abilities than most people believe. But belief plays a big role in that, your body will do what your brain believes and will not do what you don’t believe is possible. Belief is what causes placebos to work. The body gladly serves the brain. Changing one’s way of thinking often changes one’s well being. We know this at a fundamental level, positive people are usually healthier.
There very could be a good number of autoimmune difficulties from this reckless pharmaceutical experiment on millions of unwitting humans. The side effects known so far are not consistent. Everyone is unique. So its difficult to make any prediction what comes from all this other than an more awakened and activist population. This is mostly about controlling the movement of people and tracking them.
The questions asked below are the ones the news media should have asked about COVID-19, but didn’t. The elephant in the room is the American news media is almost exclusively funded by ad revenue from pharmaceutical companies. They will not run stories critical of their income stream. This is simply paycheck corruption.
How does the biggest vaccination program in history fit into the COVID-19 story? Like the pandemic itself, the vaccines the FDA raced to approve are illegitimate. Simply there is no scientific or immunological basis for making a vaccine out of RNA. In fact, using RNA as an immunogen (a substance that stimulates the production of antibodies), might be among the worst possible approaches conceivable for a vaccine. Vaccines are designed to stimulate the body’s production of antibodies, substances that can bind and neutralize germs, protecting and ridding the body against infection.
For COVD-19, it is desired to stimulate the immune system to generate antibodies that target a unique protein present on the surface of a virus, dubbed the “spike” protein.
Proteins on the surface of a virus can form repeating organized structures, like the black and white polygons on a soccer ball. When cells of the immune system interact with the virus, the repeating structures allow receptors on the immune system cells to cluster around these viral proteins. The clustering provides a strong stimulation signal to the cells of the immune system responsible for producing antibodies. When the cells receive the signal from the clustering antibodies, they can then amplify the production and build up excess reserves of antibodies against the virus. For immunization, the strategy is to create a vaccine that can mimic this natural structure of virus to efficiently and potently stimulate antibody production. When targeting a specific molecule like the spike protein of the COVID-19 virus, the most effective way to make a strong vaccine is by injecting the spike protein, which is attached to tiny particles that are around the size of a virus. This approach, discovered in 1926, was the first so called subunit vaccine (as opposed to using a preparation of the virus itself) and until recently, the only type of vaccine approved for human use in the United States.
Sticking proteins on tiny particles works so well because the way the protein assemble mimics the repeating structure of proteins on the surface of a real virus, forming the matrix which can efficiently cluster receptors on the surface of antibody producing cells.
So why for the first time in history was RNA – an untested and truly unfathomable – approach promoted for the COVID-19 vaccination program?
RNA ?s not a protein, so it cannot be organized structurally, or in any other way, to directly stimulate an antibody response against the virus. RNA is used to indirectly code for the viral protein. When injected, RNA must somehow get into cells of the body and/or immune system 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 coded protein, but we do know that it is an extremely inefficient process.
Once the RNA gets into a cell, and the cell produces the desired protein (in this case the spike protein), the protein must somehow get presented to cells of the immune system responsible for making antibodies and do so in a way that clusters the receptors and activates these cells that produce antibodies.
The RNA’s ability to get into cells and produce a protein matrix is an extremely unlikely event. Since RNA is such a remarkably ineffective immunogen, the RNA vaccine is mixed with highly toxic substances, known as adjuvants. The adjuvant ingredients are designed to somehow help the RNA get into cells. The toxic adjuvants used are intended to make up for the lack of immunogenicity of the RNA by stimulating a very potent irritation, creating a massive insult prompting large numbers of immune cells to be recruited to the site of injection. This massive inflammation can help overcome the inefficiency of the RNA and stimulate an antibody response. In addition to being a terrible immunogen for a vaccine, RNA is probably the worst possible substance for a vaccine in terms of its suitability for storage and transport. RNA needs to be kept at extremely low temperatures. A good storage condition is -112°F or in liquid nitrogen, or else the RNA breaks down into useless fragments in minutes.
The use of an RNA as a vaccination strategy seems illogical. Conventional vaccines, proven over a century, work better, are less toxic, are simple to make, and are very stable to ship and store compared to RNA. With all of these factors, the RNA vaccine is being hailed as one of the biggest feats in medical history. So why did the US government provide $billions to Moderna? Is there some kind of complicity between the parties? One needs to simply look at the timeline.
Neutralizing Antiviral Antibody Responses. Zinkernagel Et Al. 2001. Advances In Immunology, Vol. 79
|CLICK SCREEN SHOT TO ENLARGE|