It appears many are following in lockstep, lining up and eager to get their jab. They appear completely unaware that this first-ever-of-its-kind mRNA “vaccine” will not prevent them from contracting the virus nor will it prevent them from transmitting the virus. It will merely lessen the severity of their symptoms.
Yet most of those who have been tested “positive” with the highly suspect PCR test ((whose excessively high Cycle Thresholds that result in an extremely high percentage of false positives (by some experts’ accounts-over 90%) -are finally being brought to light)) exhibit and experience no symptoms in the first place.
And remember, once you get the jab you will still need to wear a mask and socially distance. So you may ask, what’s the point?
For more background, please also see:
Anyone still presuming that a Positive PCR test is showing a COVID case needs to read this very carefully
Back to this story.
So, once again, the goalposts have been moved. Now even after getting poked with a rushed experimental mRna vaccine you’ll need to continue this lockdown ritual. After the shot you’ll be monitored and tracked. You will be the experiment. That will also eventually be your ticket to participate. The idea of vaccine or immunity passports, which until now was dismissed as a conspiracy theory are being floated now to familiarize the masses with the long-planned goal.
In a heavy push to get these jabs in as many arms as possible, the propaganda machine is marching out celebrity spokespersons as heroes while ignoring the reports of adverse affects, as well as not only censoring but going as far as de-platforming those who shed light on any such information.
If our safety and well-being was really a priority wouldn’t at least the brakes be pumped and more careful steps be taken in jabbing as many arms as possible with a concoction that has been rushed through the testing and approval processes in order to get these enormously profitable potions to market?
Before we get into the long list of stories below, let’s look at this prime example of propaganda media spin and censorship.
ATLANTA (AP) — Baseball Hall of Famer Hank Aaron, former U.N. Ambassador and civil rights leader Andrew Young and former U.S. Health and Human Services Secretary Louis Sullivan got vaccinated against COVID-19 in Georgia on Tuesday, hoping to send a message to Black Americans that the shots are safe.
Getting vaccinated “makes me feel wonderful,” Aaron told The Associated Press. “I don’t have any qualms about it at all, you know. I feel quite proud of myself for doing something like this. … It’s just a small thing that can help zillions of people in this country.”
Immediately “fact-checkers” knew there was no connection to the experimental vaccine.
But have a look for yourself. Do a little digging and come to your own conclusions. And remember, after many years of unsuccessful attempts to create a vaccine against coronavirus miraculously “successful” candidates are now coming out of the woodwork.
VIDEO: panel discussion with Robert F Kennedy Jr. & Del Bigtree re: previous Mrna vaccine development
329 Deaths + 9,516 Other Injuries Reported Following COVID Vaccine, Latest CDC Data Show
The numbers reflect the latest data available as of Jan. 22 from the CDC’s Vaccine Adverse Event Reporting System website. Of the 329 reported deaths, 285 were from the U.S., and 44 were from other countries. The average age of those who died was 76.5.
As of Jan. 22, 329 deaths — a subset of 9,845 total adverse events — had been reported to the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) following COVID-19 vaccinations. VAERS is the primary mechanism for reporting adverse vaccine reactions in the U.S. Reports submitted to VAERS require further investigation before confirmation can be made that an adverse event was linked to a vaccine.
The Moderna vaccine lot numbers associated with the highest number of deaths were: 025L20A (13 deaths), 037K20A (11 deaths) and 011J2A (10 deaths). For Pfizer, the lot numbers were: EK5730 (10 deaths), EJ1685 (11 deaths), EL0140 (15 deaths), EK 9231 (12 deaths) and EL1284 (11 deaths).
Anyone suffering from a serious injury will have little legal recourse because they will be directed to the Countermeasures Injury Compensation Program which has rejected 90% of vaccine-injury claims over the past decade.
An overview of Covid-19 Vaccine Side Effects and Allergic Reactions worldwide.
Amid increasing calls for suspension of the use of mRNA-based COVID-19 vaccines produced by companies such as Pfizer, especially among elderly people, the situation in Norway has escalated significantly as the Scandi nation has now registered a total of 29 deaths among people over the age of 75 who’ve had their first COVID-19 vaccination shot.
Deaths have occurred among people receiving both the Moderna and the Pfizer-BioNTech vaccines, according to the reports.
In addition to the deaths, people have reported 96 life-threatening events following COVID-19 vaccinations, as well as 24 permanent disabilities, 225 hospitalizations, and 1,388 emergency room visits.
It’s not just the old and frail, in Israel, which proudly lays claim to the greatest vaccination effort in the world (largest percentage of the population inoculated),
As RT reports, at least 13 Israelis have experienced facial paralysis after being administered the Pfizer Covid-19 vaccine, a month after the US Food and Drug Administration reported similar issues but said they weren’t linked to the jab.
Israeli outlet Ynet reported, citing the Health Ministry, that officials believe the number of such cases could be higher.
“For at least 28 hours I walked around with it [facial paralysis],” one person who had the side effect told Ynet.
“I can’t say it was completely gone afterwards, but other than that I had no other pains, except a minor pain where the injection was, but there was nothing beyond that.”
Ynet quoted Prof. Galia Rahav, director of the Infectious Diseases Unit at Sheba Medical Center, who said she did not feel “comfortable” with administering the second dose to someone who had received the first jab and subsequently suffered from paralysis.
“No one knows if this is connected to the vaccine or not. That’s why I would refrain from giving a second dose to someone who suffered from paralysis after the first dose,” she told the outlet.
Finally, as we noted yesterday following the news of rising post-vaccination deaths in Noway, health experts from Wuhan, China, called on Norway and other countries to suspend the use of mRNA-based COVID-19 vaccines produced by companies such as Pfizer, especially among elderly people.
HURON, Ohio, January 27, 2021 (LifeSiteNews) — A 39-year-old woman with no known comorbidities died unexpectedly in northern Ohio within 48 hours of receiving a COVID-19 vaccine, which was reportedly required by her employer.
Janet L. Moore, a nurse aide at Admirals Pointe Nursing Home (APNH) in Huron, was found unresponsive in her car outside her apartment complex on December 31 around 8:00 p.m., her brother Jacob Gregory told LifeSiteNews.
“She was coming home from work and as soon as she drove into her parking lot she passed away,” he said. “According to her neighbors she wasn’t feeling good directly after the vaccine, and then ever since the vaccine she was actually feeling nauseated, she’d have like migraines and stuff like that. And then, within 48 hours, she ended up passing away.”
Gregory mentioned that his deceased sister, a mother of two sons, was required to receive this vaccine due to her nursing home employment.
Nearly a dozen employees were forced from their jobs due to the policy, and 27 wrote letters of complaint seeking to have the policy changed.
Their concerns included how this biological agent, which was rushed through development and testing, may have dangerous, unknown long-term effects, while others expressed worries about it affecting their pregnancy or fertility.
SANTA ANA (CBSLA) – A 60-year-old Orange County man died after receiving a second dose of the coronavirus vaccine. Now investigators are trying to determine if the vaccination played any role in his death.
Hours after getting his second Pfizer dose on January 5, Tim Zook was in the emergency room of the hospital where he worked.
He fell into a coma within two days and passed away four days after getting the shot.
“In my mind his death was 100 percent linked to the vaccine. There is no other explanation,” she said. “He was in very good health. He didn’t smoke, he drank alcohol once in a while but only socially. He worked out, we had kayaks, he was a deep sea fisherman,” she added.
What’s more, the doctor started to experience unusual symptoms, and three days after vaccination, small spots began to appear on Gregory Michael’s feet and hands. In response, he went to the emergency room at Mount Sinai. As his blood count was not in the normal ranges, he was admitted to the ICU, his wife told Sputnik. Shortly after, he suffered a stroke and died.
Three days after vaccination, small spots began to appear on Gregory Michael’s feet and hands. In response, he went to the emergency room at Mount Sinai. As his blood count was not in the normal ranges, he was admitted to the intensive care unit, according to Heidi Neckelmann. Unfortunately, shortly after, he suffered a stroke and died.
According to Darren Caprara, director of operations at the Miami-Dade medical examiner’s office, Gregory Michael’s death is the first that the county medical examiner’s office has seen where a COVID-19 vaccine could have played a role.
Earlier, Carlos Palestino, the brother-in-law of Mexican doctor Karla Cecilia Perez, was paralyzed hours after receiving the Pfizer/BioNTech COVID-19 vaccine, according to reports.
Moderna acknowledges receiving a report from the California Department of Public Health (CDPH) that several individuals at one vaccination center in San Diego were treated for possible allergic reactions after vaccination from one lot of Moderna’s COVID-19 Vaccine.
Lynch, who had already received both doses of Pfizer’s coronavirus vaccine, was tested for the virus after a staff member in his Boston office tested positive earlier in the week. The congressman received his positive test Friday afternoon.
New York Rep. Adriano Espaillat has tested positive for COVID-19 — after completing his vaccination against the virus last week.
“I am following guidance from my physician and quarantining at home after having tested positive for COVID-19,” wrote Espaillat, 66.
Dec 30 (Reuters) – A nurse in California tested positive for COVID-19 more than a week after receiving Pfizer Inc’s vaccine, an ABC News affiliate reported https://bit.ly/2L8iBel on Tuesday, but a medical expert said the body needs more time to build up protection.
“At this stage it is still difficult to draw definitive conclusions about the effectiveness of the vaccine, for better or worse.”
(Covid-19 Vaccine Side Effects World Map – bit.ly/vaxxmap)
“A Jefferson County woman who received a COVID-19 vaccine said a lymph node in her armpit swelled to the size of a golf ball days later. Misty Russell received a Moderna vaccine from a batch linked to six allergic reactions at a site in San Diego.”
46-year old healthcare worker dies day after receiving COVID-19 vaccine; govt says death not related to jab
By ROMEO F. QUIJANO, M.D.
Department of Pharmacology and Toxicology
College of Medicine, University of the Philippines Manila
The COVID-19 (SARS-Cov-2) vaccine is fraught with hazards. This should be the obvious, rational conclusion of anyone who cares to objectively study the available scientific and other relevant information about it. There are many factual danger signals that are easily discernible.
During the 2002-2003 SARS-1 outbreak, it took about 20 months before a vaccine was made ready for human testing in clinical trials despite the fact that concerns about safety were still unresolved. This was already way too fast compared to the usual time necessary for pre-clinical trials or animal studies to be satisfactorily completed before any ethical experimentation on human beings or clinical trials can be started. Yet for Covid-19 candidate vaccines, clinical trials were started barely five months after SARS-Cov-2 emerged, bypassing the necessary pre-clinical studies normally required and ignoring the serious safety concerns in the previous attempt to rush a SARS-1 vaccine (which was eventually scrapped).
One major safety concern in developing a vaccine is how to get around the danger that the vaccine might actually “enhance” the pathogenicity of the virus, or make it more aggressive possibly due to antibody-dependent enhancement (ADE), as what happened with previous studies on test vaccines in animals. If that should happen in a major human trial the outcome could be disastrous. (1,2,3,4) This serious adverse effect may not even be detected by a clinical trial especially in highly biased clinical trials laden with conflicts of interest involving vaccine companies. Even when a serious adverse event is detected, this is usually swept under the rug.
For example, initial clinical trial results for the COVID-19 vaccine of Moderna reportedly showed that three of the 15 human experimental subjects in the high dose group suffered serious and medically significant symptoms. Moderna, however, concluded that the vaccine was “generally safe and well tolerated,” which the corporate-dominated media dutifully reported, covering-up the real danger from the vaccine.(5,6,7,8) In a brazen act of unethical behaviour, Moderna even used a volunteer vaccine recipient, Ian Haydon, to appear in many appearances on media promoting Moderna’s experimental COVID-19 vaccine. Moderna encouraged Haydon to appear on TV to deceive the public and its shareholders. Less than 12 hours after vaccination, Haydon suffered muscle aches, vomiting, spiked a 103.2 degree fever and had lost consciousness.(9) The vaccine, pushed by Dr. Anthony Fauci, director of the US National Institute of Allergy and Infectious Diseases, and financed by Bill Gates, used an experimental mRNA technology that supposedly would allow rapid deployment, waiving the usual pre-clinical and animal studies.
The fact that an entirely new RNA vaccine technology which has never been used before in humans is a danger signal that should not be ignored. Several of the US candidates (Moderna, Pfizer/BioNTech, and Arcturus Therapeutics) are using this never-before-approved technology. Exogenous mRNA is inherently immunostimulatory, and this feature of mRNA could be beneficial or detrimental. It may provide adjuvant activity and it may inhibit antigen expression and negatively affect the immune response. The paradoxical effects of innate immune sensing on different formats of mRNA vaccines are incompletely understood. Potential safety concerns include local and systemic inflammation, biodistribution and persistence of expressed immunogen, stimulation of auto-reactive antibodies, and potential toxic effects of non-native nucleotides and delivery system components. A mRNA-based vaccine could also induce potent type I interferon responses, which have been associated not only with inflammation but also potentially with autoimmunity. Another potential safety issue could derive from the extracellular RNA which has been shown to increase the permeability of tightly packed endothelial cells and may promote blood coagulation and pathological thrombus formation. (10)
Another danger of mRNA vaccines is the use of biotech “carrier systems” involving lipid nanoparticles (LNPs). LNPs “encapsulate the mRNA constructs to protect them from degradation and promote cellular uptake,” and additionally, rev up the immune system. The LNP formulations in the three mRNA Covid-19 vaccines are also “PEGylated,” meaning that the vaccine nanoparticles are coated with a synthetic, non-biodegradable and increasingly controversial polymer called polyethylene glycol (PEG). LNPs could contribute to one or more of the following: immune reactions, infusion reactions, complement reactions, opsonation reactions, antibody reactions or reactions to the PEG from some lipids or PEG otherwise associated with the LNP, as well as adverse reactions within liver pathways or degradation of the mRNA or the LNP, any of which could lead to significant adverse events. Furthermore, PEG can also provoke severe neuropsychiatric symptoms in offsprings, including mood swings, rage, phobias and paranoia. Investigators who once assumed that the polymer was largely “inert” are now questioning its biocompatibility and warning about PEGylated particles’ promotion of tumor growth and adverse immune responses that include “probably underdiagnosed” life-threatening anaphylaxis. This is a significant concern since a 2016 US study reported detectable and sometimes high levels of anti-PEG antibodies (including first-line-of-defense IgM antibodies and later-stage IgG antibodies) in approximately 72% of contemporary human samples and about 56% of historical specimens from the 1970s through the 1990s. The manufacturers of genetically engineered adenoviral vector COVID-19 vaccines undergoing clinical trials (Johnson & Johnson, Oxford, and CanSino) also use PEG as an inexpensive additive for vaccine storage. If one of the PEGylated mRNA vaccines for Covid-19 gains approval, the increased exposure to PEG will be unprecedented and potentially disastrous. (11,12)
Like the mRNA vaccines, the adenoviral vector COVID-19 vaccines are still experimental and have not been used before in mass vaccination for infectious diseases. Given the history of poor safety record of many vaccines, the risk of unpredictable and potentially disastrous adverse effects is of utmost concern.
For example, among other dangers, the virus-vectored vaccines could undergo recombination with naturally occurring viruses and produce hybrid viruses that could have undesirable properties affecting transmission or virulence. The numerous variables affecting the probability that recombination will take place and the possible outcomes of recombination are practically impossible to quantify accurately given existing tools and knowledge. The risks, however, are real, as exemplified by the emergence of mutant types of viruses, enhanced pathogenicity and unexpected serious adverse events (including death) following haphazard mass vaccination campaigns and previous failed attempts to develop chimeric vaccines using genetic engineering technology.
Genetically engineered vaccines carry significant unpredictability and a number of inherent harmful potential hazards, including unintended and unwanted side effects with regard to the targeted or non-targeted individuals. Potential undesirable immunological effects include unexpected immunopathological reaction, autoimmune reaction, long-term tolerance, persistent infection and latent infections. There is also the potential to transfer or recombine genetic material from genetically engineered viruses or GE virus-vector vaccines to the targeted individual germ line cells. It can also undergo chromosomal integration or insertional mutagenesis, leading to random insertions of vaccine constructs into host cellular genomes, resulting in alterations of gene expression or activation of cellular oncogenes, thus raising the possibility of inducing tumors. Even minor genetic changes in, or differences between, viruses can result in dramatic changes in transmission abilities, host preferences, and virulence. The new, hybrid virus progenies resulting from such events may have completely unpredictable characteristics. Virulence reversion, for example, was documented when a live recombinant vaccinia–rabies glycoprotein virus vaccine prepared for wild raccoons and foxes infected a 28-yr-old pregnant woman. (13) Virulence reversion was also documented when recombination between commercial infectious laryngotracheitis virus (ILTV) vaccines in poultry has resulted in virulent recombinant viruses that caused severe disease and that have emerged as the dominant field strains in important poultry producing regions in Australia. (14)
The risks of recombination was actually raised earlier in a meeting convened by the World Health Organization in 2003, wherein regulators representing the European Union, the US, China, and Canada raised the specific issue on recombination: “Recombination of a live virus-vectored vaccine with a circulating or reactivated latent virus could theoretically generate a more pathogenic strain…The risk of recombination should be studied if possible in a non-clinical model system, but should also be considered in clinical study designs.” This was listed among the “recommendations to WHO and priorities for future work” as one of several “issues of critical importance to be investigated further.” (15) Apparently, however, the WHO, governments and the vaccine industry never took this recommendation seriously. This comes as no surprise, given the history of WHO’s rapid approval and endorsement of several such live virus-vectored vaccines without the necessary and thorough safety studies, made especially concerning during the current mad scramble for a COVID-19 vaccine.
There’s also a concern that some people may already be immune to the adenovirus carrying the coronavirus gene into the body since adenoviruses circulate through the human population making the vaccine ineffective. (16) Data on the initial clinical trial of the adenoviral vector COVID-19 vaccine made by CanSino Biologics of China that was published in the Lancet showed that in the highest of the three doses used in the study, the number of side effects was high — 75% of the people in the highest dose group reported at least one side effect. Side effects included fever — pain at the injection site, headache, fatigue, among others. Ten volunteers (9% of the overall study group) had Grade 3 side effects, defined as “serious and medically significant symptoms,” six (17%) in the highest dose group and two (6%) each in the low and middle dose groups. The study also found that one dose of the vaccine, tested at three different levels, appeared to induce a good immune response in some subjects. But about half of the volunteers — people who already had immunity to the backbone of the vaccine — had a dampened immune response. (17)
The Dengvaxia vaccine fiasco in the Philippines also illustrates the danger of rushing a vaccine and allowing corporate interests driven by market forces to address people’s health needs. As a result, many of the vaccinated suffered or died after a botched mass vaccination program.(18) According to the Chief Pathologist of the Public Attorney’s Office, 153 of those vaccinated with Dengvaxia had died as of February 18, 2020. (19)
Another example of the danger of corporate fast-tracking of vaccine clinical safety trials is the case of the HPV (Human Papilloma Virus) vaccine. Two of the biggest vaccine manufacturers spiked their placebos with a neurotoxic aluminum adjuvant and cut observation periods. Numerous adverse events, including life-threatening injuries, permanent disabilities, hospitalizations and deaths, were later reported after vaccination with bivalent, quadrivalent or nine-valent HPV vaccines. The company scientists routinely dismissed, minimized or concealed those injuries using statistical gimmicks and invalid comparisons designed to diminish their relative significance. Some regulatory agencies were complicit in covering up increased incidence of adverse effects in post-marketing surveillance studies.(20, 21)
Another concern is that vaccines produced with cell cultures are often contaminated with naked nucleic acids, genomic fragments, retroviruses and other foreign materials that carry uncertain but potentially serious hazards. This contamination may be present in the source material, e.g. human blood, human or animal tissues, cell banks, or introduced in the manufacturing process through the use of animal sera. Many candidate COVID-19 vaccines are produced on what is called “immortal” cell lines or cancerous types of cells (e.g. Vero cells derived from the African green monkey) that could spread cancer-promoting material into the human recipient. Manufacturers and authorities assure us that these do not cause tumors per se. However, scientific studies tell us that after these cells have been repeatedly cultured a certain number of times, they can convert to a cancerous state. Immortal cell lines show 100-times greater number of DNA recombination events compared to normal cells. This could result in viral-viral or viral-cellular interactions that can generate new viruses and result to pathological consequences, including autoimmunity and cancer. (22) Even the US FDA recognized this danger. In a paper published in its website, it stated: “In some cases the cell lines that are used might be tumorigenic, that is, they form tumors when injected into rodents. Some of these tumor-forming cell lines may contain cancer-causing viruses that are not actively reproducing. Such viruses are hard to detect using standard methods. These latent, or ‘quiet,’ viruses pose a potential threat, since they might become active under vaccine manufacturing conditions.” (23)
Still another concern, not only in terms of safety issues but also on moral grounds, is the use of aborted fetal cells in vaccine manufacture. Vaccines produced from human fetal cells contain cell debris and contaminating fetal DNA (together with its epigenetic modification) which cannot be fully eliminated during downstream purification. This could cause insertional mutagenesis (potentially causing cancer) and autoimmunity in the vaccinated. At least six of the COVID-19 candidate vaccines (Cansino, AstraZeneca/Oxford, Janssen, ImmunityBio/NantKwest, University of Pittsburgh and Altimmune) use one of two human fetal cell lines: HEK-293, a kidney cell line that comes from a fetus aborted in about 1972; and PER. C6, a proprietary cell line owned by Janssen, developed from retinal cells from an 18-week-old fetus aborted in 1985. (24)
There are many plausible biological mechanisms for potential adverse effects of all the vaccines in the pipeline for COVID-19. The history of vaccination is replete with scientific evidence of adverse effects through enhanced pathogenicity, mutation, recombination, induced immune system dysfunction, and various non-specific effects following vaccination despite regulatory approval and prior clinical trials and other corporate sponsored studies that were claimed to be proof of safety. The inherent danger of injecting microbial protein fragments, contaminants, DNA and other foreign materials into the human body is well documented in the scientific literature. Practically all vaccines contain such hazardous foreign fragments and materials and are unavoidably unsafe. Furthermore, exposure of the vaccinee to other environmental hazards (pesticides, air pollutants, 5G radiation, ionizing radiation, etc.) resulting to synergistic adverse effects not captured by corporate sponsored “safety” studies is also another plausible mechanism that may result in acute or long-term injury, including death.
Safety assessments under the corporate dominated scientific milieu are grossly inadequate and oftentimes erroneous. Pre-clinical studies and clinical trials are done or sponsored by the very corporations who sell the vaccines and they do not adequately address the plausible adverse effects that cannot be detected by the corporate sponsored studies. There are no independent studies that could validate the claims of the vaccine manufacturers. Therefore, there is no reason to believe that the potential benefits from an upcoming COVID-19 vaccine would outweigh the potential adverse effects, despite assurances of safety by the vaccine industry, international institutions, governments and the mainstream medical science groups.
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