RFK, Jr. Warned FDA Three Months Ago About Ingredient in Pfizer COVID Vaccine That Likely Caused Life-Threatening Reaction in Two UK Healthcare Workers

RFK, Jr. Warned FDA Three Months Ago About Ingredient in Pfizer COVID Vaccine That Likely Caused Life-Threatening Reaction in Two UK Healthcare Workers
An investigation this week identified polyethylene glycol (PEG) as the likely reason two people in the UK suffered anaphylaxis after receiving Pfizer’s COVID vaccine. In September, CHD Chairman RFK, Jr. warned the FDA that PEG in COVID vaccines could lead to severe allergic

by Lyn Redwood, RN, MSN, The Defender, Children’s Health Defense
December 11, 2020

 

On Dec. 2, Britain’s Medicines and Healthcare Products Regulatory Agency (MHRA) became the first in the world to approve a COVID-19 vaccine developed by Germany’s BioNTech and Pfizer.

A mass vaccination campaign that targeted frontline workers to receive the vaccine began on Dec. 8. Within 24 hours of launching the campaign, MHRA acknowledged two reports of anaphylaxis and one report of a possible allergic reaction.

Reuters reported late yesterday afternoon that an investigation into the anaphylactic reactions by MHRA has identified polyethylene glycol, or PEG, as the likely culprit.

Imperial College London’s Paul Turner, an expert in allergy and immunology who has been advising the MHRA on its revised guidance, told Reuters: “The ingredients like PEG which we think might be responsible for the reactions are not related to things which can cause food allergy. Likewise, people with a known allergy to just one medicine should not be at risk.”

It was also reported that PEG, which helps to stabilize the shot, is not in other types of vaccines.

The statements by Turner that “PEG is not in other types of vaccines” and that people with allergies to “just one medicine should not be at risk” are a failed attempt to provide false assurances and are patently untrue.

Moderna, Pfizer/BioNTech and Arcturus Therapeutics COVID vaccines all utilize a never-before-approved messenger RNA (mRNA) technology, an experimental approach designed to turn the body’s cells into viral protein-making factories. This technology involves the use of lipid nanoparticles (LNPs) that encapsulate the mRNA to protect them from degradation and promote cellular uptake.

The LNP formulations in the three COVID-19 mRNA vaccines are “PEGylated,” meaning that the vaccine nanoparticles are coated with a synthetic, non-degradable and increasingly controversial PEG.

COVID mRNA vaccines are not the only vehicle for PEG involvement in COVID-19 vaccine production. Researchers at Germany’s Max Planck Institute report developing a process for COVID-19 vaccine production to purify virus particles at “high yield.” The process involves adding PEG to a virus-containing liquid and passing the liquid through membranes.

On Sept. 25, Robert F. Kennedy, Jr., chairman and chief legal counsel for Children’s Health Defense (CHD), notified the Steven Hahn, director of the U.S. Food and Drug Administration (FDA), Dr. Peter Marks director of FDA’s Center for Biologics Evaluation and Research and Anthony Fauci, director of the National Institute for Allergy and Infectious Diseases, of the serious and possibly life-threatening anaphylactic potential of PEG.

CHD received the following response from the FDA, on Dec. 2, but has not yet received a response from Fauci.

 

In earlier communications with Moderna scientists regarding the controversial use of PEG in the company’s COVID-19 vaccine due to the potential for life-threatening anaphylaxis and need for pre-screening for PEG antibodies prior to vaccine administration, they insisted that the existence of PEG antibodies was purely hypothetical and underserving of concern:

“Pre-screening populations based on hypothesized biomarkers, such as anti-PEG antibodies, is not a strategy currently employed in our clinical trials.”

Given the recent evidence of PEG anaphylaxis in Pfizer mRNA vaccine recipients, I wonder if FDA and vaccine manufacturers will now reconsider their position.

An extensive review of PEG therapeutics, published in 2013, documented adverse effects of PEGylation and questioned the wisdom behind the continued use of PEG in drug development. The authors concluded that “the accumulating evidence documenting the detrimental effects of PEG on drug delivery make it imperative that scientists in this field break their dependence on PEGylation.”

The statement by Turner that “people with a known allergy to just one medicine should not be at risk,” is also not true.

2018 study, “Immediate Hypersensitivity to Polyethylene Glycols and Polysorbates: More Common Than We Have Recognized” reports there are more than 1,000 products, including prescription drugs, that contain PEG. (See chart below for detailed descriptions of PEG containing drugs.)

The decision to allow people with other medication allergies to receive vaccines that utilize PEG in the manufacturing or delivery of the vaccine is a very risky proposition — especially given that Pfizer has said people with a history of severe adverse allergic reactions to vaccines or the candidate’s ingredients were excluded from their late stage trials.

We have no idea what the incidence of allergy or anaphylactic reactions will be once Pfizer begins global distribution of the vaccine, without such exclusions.

2016 study reported detectable and sometimes high levels of anti-PEG antibodies in approximately 72% of contemporary human samples and about 56% of historical specimens from the 1970s through the 1990s. The population’s increased exposure to PEG-containing products since the 1990’s makes it natural to assume that anti-PEG antibodies will continue to be widespread.

As approval of PEGylated mRNA vaccines for COVID-19 occurs, the uptick in exposure to injected PEG products will be unprecedented and potentially disastrous.

While four out of five doctors regularly prescribe PEGylated drugs, only one out of five are aware of the potential for anti-PEG antibody responses. And only a third even know that PEG is in the drugs that they are prescribing.

A Vanderbilt University researcher agrees that there is a widespread lack of recognition that PEG hypersensitivity is possible, much less that it manifests on a regular basis. While it has been recommended to screen patients for anti-PEG antibody levels “prior to administration of therapeutics containing PEG” such testing is currently only available in research settings.

In a declaration effective Feb. 4, the Secretary of Health and Human Services invoked the Public Readiness and Emergency Preparedness Act (PREP Act) and declared Coronavirus Disease 2019 (COVID-19) to be a public health emergency warranting liability protections for covered countermeasures, including vaccines.

The fact that the FDA has abdicated its responsibility for assuring the safety of COVID vaccines to vaccine  manufacturers means we are on our own to study the science, and weigh the benefits and risks of all drugs and vaccines.

CHD will continue to monitor this important safety issue in an effort to keep you well informed on the science and public policies surrounding COVID-19 vaccine development.

Descriptions of PEG containing drugs:

 




COVID Vaccine—History Matters

COVID Vaccine—History Matters

by Jon Rappoport, No More Fake News
December 11, 2020

 

Now that governments are going to roll out “a vaccine to save the world” (see here and here), people should become aware of a history they don’t know exists.

The article below was a small section of my book, AIDS INC., which I wrote in 1987-8. At the time, I decided to take a look at vaccines and see what I could find out about them.

My ensuing research led me into all sorts of surprising areas.

Since the period of 1987-8, much more has come to light about vaccine safety and efficacy. Here is what I discovered way back when—


“The combined death rate from scarlet fever, diphtheria, whooping cough and measles among children up to fifteen shows that nearly 90 percent of the total decline in mortality between 1860 and 1965 had occurred before the introduction of antibiotics and widespread immunization. In part, this recession may be attributed to improved housing and to a decrease in the virulence of micro-organisms, but by far the most important factor was a higher host-resistance due to better nutrition.” Ivan Illich, Medical Nemesis, Bantam Books, 1977

“In a recent British outbreak of whooping cough, for example, even fully immunized children contracted the disease in fairly large numbers; and the rates of serious complications and death were reduced only slightly. In another recent outbreak of pertussis, 46 of the 85 fully immunized children studied eventually contracted the disease.

“In 1977, 34 new cases of measles were reported on the campus of UCLA, in a population that was supposedly 91% immune, according to careful serological testing. Another 20 cases of measles were reported in the Pecos, New Mexico, area within a period of a few months in 1981, and 75% of them had been fully immunized, some of them quite recently. A survey of sixth-graders in a well-immunized urban community revealed that about 15% of this age group are still susceptible to rubella, a figure essentially identical with that of the pre-vaccine era.” Richard Moskowitz, MD, The Case Against Immunizations, 1983, American Institute of Homeopathy.

“Of all reported whooping cough cases between 1979 and 1984 in children over 7 months of age – that is, old enough to have received the primary course of the DPT shots (diphtheria, pertussis, tetanus) – 41% occurred in children who had received three or more shots and 22% in children who had one or two immunizations.

“Among children under 7 months of age who had whooping cough, 34% had been immunized between one and three times…

“… Based on the only U.S. findings on adverse DPT reactions, an FDA-financed study at the University of California, Los Angeles, one out of every 350 children will have a convulsion; one in 180 children will experience high-pitched screaming; and one in 66 will have a fever of 105 degrees or more.” Jennifer Hyman, Democrat and Chronicle, Rochester, New York, special supplement on DPT, dated April, 1987.

“A study undertaken in 1979 at the University of California, Los Angeles, under the sponsorship of the Food and Drug Administration, and which has been confirmed by other studies, indicates that in the U.S.A. approximately 1,000 infants die annually as a direct result of DPT vaccinations, and these are classified as SIDS (Sudden Infant Death Syndrome) deaths. These represent about 10 to 15% of the total number of SIDS deaths occurring annually in the U.S.A. (between 8,000 and 10,000 depending on which statistics are used).” Leon Chaitow, Vaccination and Immunization, CW Daniel Company Limited, Saffron Walden, Essex, England, 1987.

“Assistant Secretary of Health Edward Brandt, Jr., MD, testifying before the U.S. Senate Committee on Labor and Human Resources, rounded… figures off to 9,000 cases of convulsions, 9,000 cases of collapse, and 17,000 cases of high-pitched screaming for a total of 35,000 acute neurological reactions occurring within forty-eight hours of a DPT shot among America’s children every year.” DPT: A Shot in the Dark, by Harris L. Coulter and Barbara Loe Fischer, Harcourt Brace Jovanovich.

“While 70-80% of British children were immunized against pertussis in 1970-71, the rate is now 39%. The committee predicts that the next pertussis epidemic will probably turn out to be more severe than the one in 1974/75. However, they do not explain why, in 1970/71, there were more than 33,000 cases of pertussis with 41 fatal cases among the very well immunized British child population; whereas in 1974/75, with a declining rate of vaccination, a pertussis epidemic caused only 25,000 cases with 25 fatalities.” Wolfgang Ehrengut, Lancet, Feb. 18, 1978, p. 370.

“… Barker and Pichichero, in a prospective study of 1232 children in Denver, Colorado, found after DTP that only 7% of those vaccinated were free from untoward reactions, which included pyrexia (53%), acute behavioral changes (82%), prolonged screaming (13%), and listlessness, anorexia and vomiting. 71% of those receiving second injections of DTP experienced two or more of the reactions monitored.” Lancet, May 28, 1983, p. 1217

“Publications by the World Health Organization show that diphtheria is steadily declining in most European countries, including those in which there has been no immunization. The decline began long before vaccination was developed. There is certainly no guarantee that vaccination will protect a child against the disease; in fact, over 30,000 cases of diphtheria have been recorded in the United Kingdom in fully immunized children.” Leon Chaitow, Vaccination and Immunization, p. 58.

“Pertussis (whooping cough) immunization is controversial, as the side effects have received a great deal of publicity. The counter claim is that the effectiveness and protection offered by the procedure far outweigh the possible ill effects… annual deaths, per million children, from this disease over the period from 1900 to the mid-nineteen seventies, shows that from a high point of just under 900 deaths per million children (under age 15) in 1905, the decline has been consistent and dramatic. There had been a lowering of mortality rates of approximately 80% by the time immunization was introduced on a mass scale, in the mid-nineteen fifties. The decline has continued, albeit at a slower rate, ever since. No credit can be given to vaccination for the major part of the decline since it was not in use.” Chaitow, Vaccination and Immunization, p. 63.

“… the swine-flu vaccination program was one of its (CDC) greatest blunders. It all began in 1976 when CDC scientists saw that a virus involved in a flu attack outbreak at Fort Dix, N.J., was similar to the swine-flu virus that killed 500,000 Americans in 1918. Health officials immediately launched a 100-million dollar program to immunize every American. But the expected epidemic never materialized, and the vaccine led to partial paralysis in 532 people. There were 32 deaths.” U.S. News and World Report, Joseph Carey, October 14, 1985, p. 70, “How Medical Sleuths Track Killer Diseases.”

“Despite (cases) in which (smallpox) vaccination plainly failed to protect the population, and despite the rampant side-effects of the methods, the proponents of vaccination continued their attempts to justify the methods by claims that the disease had declined in Europe as a whole during the period of its compulsory use. If the decline could be correlated with the use of the vaccination, then all else could be set aside, and the advantage between its current low incidence could be shown to outweigh the periodic failures of the method, and to favour the continued use of vaccination. However, the credit for the decline in the incidence of smallpox could not be given to vaccination. The fact is that its incidence declined in all parts of Europe, whether or not vaccination was employed.” Chaitow, Vaccination and Immunization, pp. 6-7.

“Smallpox, like typhus, has been dying out (in England) since 1780. Vaccination in this country has largely fallen into disuse since people began to realize how its value was discredited by the great smallpox epidemic of 1871-2 (which occurred after extensive vaccination).” W. Scott Webb, A Century of Vaccination, Swan Sonnenschein, 1898.

“In this incident (Kyoto, Japan, 1948) – the most serious of its kind – a toxic (vaccine) batch of alum-precipitated toxoid (APT) was responsible for illness in over 600 infants and for no fewer than 68 deaths.

“On 20 and 22 October, 1948, a large number of babies and children in the city of Kyoto received their first injection of APT. On the 4th and 5th of November, 15,561 babies and children aged some months to 13 years received their second dose. One to two days later, 606 of those who had been injected fell ill. Of these, 9 died of acute diphtheritic paralysis in seven to fourteen days, and 59 of late paralysis mainly in four to seven weeks.” Sir Graham Wilson, Hazards of Immunization, Athone Press, University of London, 1967.

“Accidents may, however, follow the use of this so-called killed (rabies) vaccine owing to inadequate processing. A very serious occurrence of this sort occurred at Fortaleza, Ceara, Brazil, in 1960. No fewer than 18 out of 66 persons vaccinated with Fermi’s carbolized (rabies) vaccine suffered from encephalomyelitis and every one of the eighteen died.” Sir Graham Wilson, Hazards of Immunization.

“At a press conference in Washington on 24 July, 1942, the Secretary of War reported that 28,585 cases of jaundice had been observed in the (American) Army between 1 January and 4 July after yellow fever vaccination, and of these 62 proved fatal.” Sir Graham Wilson, Hazards of Immunization.

“The world’s biggest trial (conducted in south India) to assess the value of BCG tuberculosis vaccine has made the startling revelation that the vaccine ‘does not give any protection against bacillary forms of tuberculosis.’ The study said to be ‘most exhaustive and meticulous,’ was launched in 1968 by the Indian Council of Medical Research (ICMR) with assistance from the World Health Organization (WHO) and the U.S. Centers for Disease Control in Atlanta, Georgia.

“The incidence of new cases among the BCG vaccinated group was slightly (but statistically insignificantly) higher than in the control group, a finding that led to the conclusion that BCG’s protective effect ‘was zero.’” New Scientist, November 15, 1979, as quoted by Hans Ruesch in Naked Empress, Civis Publishers, Switzerland, 1982.

“Between 10 December 1929 and 30 April 1930, 251 of 412 infants born in Lubeck received three doses of BCG vaccine by the mouth during the first ten days of life. Of these 251, 72 died of tuberculosis, most of them in two to five months and all but one before the end of the first year. In addition, 135 suffered from clinical tuberculosis but eventually recovered; and 44 became tuberculin-positive but remained well. None of the 161 unvaccinated infants born at the time was affected in this way and none of these died of tuberculosis within the following three years.” Hazards of Immunization, Wilson.

“We conducted a randomized double-blind placebo-controlled trial to test the efficacy of the 14-valent pneumococcal capsular polysaccharide vaccine in 2295 high-risk patients… Seventy-one episodes of proved or probable pneumococcal pneumonia or bronchitis occurred among 63 of the patients (27 placebo recipients and 36 vaccine recipients)… We were unable to demonstrate any efficacy of the pneumococcal vaccine in preventing pneumonia or bronchitis in this population.” New England Journal of Medicine, November 20, 1986, p. 1318, Michael Simberkoff et al.

“But already before Salk developed his vaccine, polio had been constantly regressing; the 39 cases out of every 100,000 inhabitants registered in 1942 had gradually diminished from year to year until they were reduced to only 15 cases in 1952… according to M. Beddow Baylay, the English surgeon and medical historian.” Slaughter of the Innocent, Hans Reusch, Civitas Publishers, Switzerland, and Swain, New York, 1983.

“Many published stories and reports have stated, implied and otherwise led professional people and the public to believe that the sharp reduction of cases (and of deaths) from poliomyelitis in 1955 as compared to 1954 is attributable to the Salk vaccine… That it is a misconception follows from these considerations. The number of children inoculated has been too small to account for the decrease. The sharp decrease was apparent before the inoculations began or could take effect and was of the same order as the decrease following the immediate post-inoculation period.” Dr. Herbert Ratner, Child and Family, vol. 20, no. 1, 1987.

“So far it is hardly possible to gain insight into the extent of the immunization catastrophe of 1955 in the United States. It may be considered certain that the officially ascertained 200 cases (of polio) which were caused directly or indirectly by the (polio) vaccination constitute minimum figures… It can hardly be estimated how many of the 1359 (polio) cases among vaccinated persons must be regarded as failures of the vaccine and how many of them were infected by the vaccine. A careful study of the epidemiologic course of polio in the United States yields indications of grave significance. In numerous states of the U.S.A., typical early epidemics developed with the immunizations in the spring of 1955… The vaccination incidents of the year 1955 cannot be exclusively traced back to the failure of one manufacturing firm.” Dr. Herbert Ratner, Child and Family, 1980, vol. 19, no. 4, “Story of the Salk Vaccine (Part 2).”

“Suffice it to say that most of the large (polio) epidemics that have occurred in this country since the introduction of the Salk vaccine have followed the wide-scale use of the vaccine and have been characterized by an uncommon early seasonal onset. To name a few, there is the Massachusetts epidemic of 1955; the Chicago epidemic of 1956; and the Des Moines epidemic of 1959.” Dr. Herbert Ratner, Child and Family, 1980 vol. 19, no. 4.

“The live (Sabin) poliovirus vaccine has been the predominant cause of domestically arising cases of paralytic poliomyelitis in the United States since 1972. To avoid the occurrence of such cases, it would be necessary to discontinue the routine use of live poliovirus vaccine.” Jonas Salk, Science, March 4, 1977, p. 845.

“By the (U.S.) government’s own admission, there has been a 41% failure rate in persons who were previously vaccinated against the (measles) virus.” Dr. Anthony Morris, John Chriss, BG Young, “Occurrence of Measles in Previously Vaccinated Individuals,” 1979; presented at a meeting of the American Society for Microbiology at Fort Detrick, Maryland, April 27, 1979.

“Prior to the time doctors began giving rubella (German measles) vaccinations, an estimated 85% of adults were naturally immune to the disease (for life). Because of immunization, the vast majority of women never acquire natural immunity (or lifetime protection).” Dr. Robert Mendelsohn, Let’s Live, December 1983, as quoted by Carolyn Reuben in the LA WEEKLY, June 28, 1985.

“Adminstration of KMV (killed measles vaccine) apparently set in motion an aberrant immunologic response that not only failed to protect children against natural measles, but resulted in heightened susceptibility.” JAMA Aug. 22, 1980, vol. 244, p. 804, Vincent Fulginiti and Ray Helfer. The authors indicate that such falsely protected children can come down with “an often severe, atypical form of measles. Atypical measles is characterized by fever, headache… and a diverse rash (which)… may consist of a mixture of macules, papules, vesicles, and pustules… ”


The above quotes reflect only a mere fraction of an available literature which shows there is a need for an extensive review of vaccination. It is certain that undisclosed, unlooked for illness occurs as a result of vaccines, or as a result of infection after protective immunity should have been conferred but wasn’t. A certain amount of this sort of illness is immunosuppressive in the widest sense, and some in a narrower sense (depression of T-cell numbers, etc.). When looking for unusual illness and immune depression, vaccines are one of those areas which remain partially hidden from investigation. That is a mistake. It is not adequate to say, “Vaccines are simple; they stimulate the immune system and confer immunity against specific germ agents.” That is the glossy presentation. What vaccines often do is something else. They engage some aspect of the body’s immune-response, but to what effect over the long term? Why, for example, do children who have measles vaccine develop a susceptibility to another more severe, atypical measles? Is that virulent form of the disease the result of reactivation of the virus in the vaccine?

Official reports on vaccine reactions are often at odds with unofficial estimates because of the method of analysis used. If vaccine-reaction is defined as a small set of possible effects experienced within 72 hours of an inoculation, then figures will be smaller. But doctors like G.T. Stewart, of the University of Glasgow, have found through meticulous investigation, including visits to hospitals and interviews with parents of vaccinated children, that reactions as severe as brain-damage (e.g., from the DPT vaccine) can be overlooked, go unreported and can be assumed mistakenly to have come from other causes.




Vaccine Study Costs Doctor His License

Vaccine Study Costs Doctor His License

by Del Bigtree w/ Dr. Paul Thomas, MD
December 11, 2020

 



Oregon Pediatrician Dr. Paul Thomas, MD has come under fire by the Oregon Medical Board for providing informed consent to his patients.

After publishing a study using the data from his more than 13000 patients, the Oregon Medical, in an attempt to silence the highly controversial study results, suspended his license.

#PaulThomas #InformedConsent #VaccineSafety #Oregon




CNN: ‘Don’t Be Alarmed’ if People Start Dying After Taking the Vaccine

CNN: ‘Don’t Be Alarmed’ if People Start Dying After Taking the Vaccine
“That won’t necessarily have anything to do with the vaccine.” 

by Paul Joseph Watson, Summit News
December 8, 2020

 

In an article on the COVID vaccine rollout, CNN says that Americans shouldn’t be alarmed if people start dying after taking the vaccine because “deaths may occur that won’t necessarily have anything to do with the vaccine.”

The advisory appeared in an article titled ‘Why vaccinate our most frail? Odd vote out shows the dilemma’ in which Dr. Kelly Moore, associate director of the Immunization Action Coalition, cautions that vaccines don’t work as well on the frail and elderly compared to healthy people.

“When shots begin to go into arms of residents, Moore said Americans need to understand that deaths may occur that won’t necessarily have anything to do with the vaccine,” states the report.

“We would not at all be surprised to see, coincidentally, vaccination happening and then having someone pass away a short time after they receive a vaccine, not because it has anything to do with the vaccination but just because that’s the place where people at the end of their lives reside,” Moore said.

She then said Americans shouldn’t be alarmed to see people dying a day or two after receiving the COVID vaccination.

“One of the things we want to make sure people understand is that they should not be unnecessarily alarmed if there are reports, once we start vaccinating, of someone or multiple people dying within a day or two of their vaccination who are residents of a long-term care facility. That would be something we would expect, as a normal occurrence, because people die frequently in nursing homes.”

While deaths in care homes of people who take the vaccine are described as normal and nothing to do with the vaccine, some would suggest that you could make the exact same argument about deaths of those with multiple comorbidities in care homes that were put down to COVID.

Many have and have been shouted down for doing so.

Connect with Paul Joseph Watson at Summit News




Sausage Making at FDA: How Human Cancer Cells Got Into Vaccines

Sausage Making at FDA: How Human Cancer Cells Got Into Vaccines
In a 2012 meeting, the FDA voted to allow the use of human fetal cells and adult human tumor cells in vaccines, despite acknowledging the many risks, including that vaccine recipients might later develop cancer.

by Robert F. Kennedy, Jr., The Defender, Children’s Health Defense
December 10, 2020

 

“If the American people knew some of the things that went on at the FDA, they’d never take anything but Bayer aspirin.” — Len Lutwalk, FDA scientist
“The FDA, by spinelessly knuckling under to every whim of the drug companies, has thrown away its high reputation, and in doing so, forfeited our trust.” — Drummond Rennie, deputy editor of JAMA
“[The] honest employee fears the dishonest employee. There is also irrefutable evidence that managers at CDER (Center for Drug Evaluation and Research of the FDA) have placed the nation at risk by corrupting the evaluation of drugs and by interfering with our ability to ensure the safety and efficacy of drugs. While I was at FDA, drug reviewers were clearly told not to question drug companies and that our job was to approve drugs … If we asked questions that could delay or prevent a drug’s approval — which of course was our job as drug reviewers — management would reprimand us, reassign us, hold secret meetings about us or worse … When you are able to dig in, if you found issues that would make you turn down a drug, you could be pressured to reverse your decision, or the review would then be handed off to someone who would simply copy and paste whatever claims the company made in the summary document … I believe I also have documentation of falsification of documents, fraud, perjury and widespread racketeering, including witnesses tampering and witness retaliation.” — Ronald Kavanagh, Ph.D., pharmacist who reviewed medications for the FDA from 1998 to 2008
Vaccines and related biological products advisory committee today

Today — Thursday, Dec. 10 — the Vaccines and Related Biological Products Advisory Committee (VRBPAC), which is the U.S. Food and Drug Administration’s (FDA) internal panel that licenses new vaccines as “safe and effective,” will meet to consider Pfizer’s COVID vaccine. VRBAC will meet in one week, Dec. 17, to consider approval of the Moderna vaccine.

The damning safety studies in Pfizer’s late release clinical trial data dump, and the severe (life-threatening) allergic reactions that bedeviled the vaccine’s UK rollout, have raised red flags and public anxiety about the safety of the companies’ mRNA vaccines. Anthony Fauci has addressed growing skepticism about COVID vaccines and the Operation Warp Speed program, by reassuring the public that “VRBPAC” is an “independent panel of leading experts” whom the public can absolutely trust to assure vaccine safety.

In order to help you make your own conclusion about how reliably VRBPAC will protect your health, I excerpt below the transcripts from the cavalier, ignorant and astonishingly unethical deliberations during the 2012 VRBPAC meeting where panelists voted unanimously to allow use of human tumor cells in vaccines. I urge you to read and make up your own mind whether you want to place your health — and perhaps your life — in the hands of these reckless charlatans and irresponsible clowns.

How FDA originally approved use of fetal cells in vaccines

FDA allows both human fetal cells and adult human tumor cells in vaccines. Both types have cancer risks. While both Pfizer and Moderna tested their mRNA vaccine using fetal cells, there are no fetal cells, cell debris or DNA in their final products.

However, according to company documents, Johnson and Johnson (Janssen) and Altimmune’s COVID vaccines are manufactured in the human fetal cell line PER-C6, and thus the final vaccine products will contain cellular debris and DNA fragments from these cells. Researchers harvested these cell lines from the eyeball of an 18-week-old human fetus aborted in 1985, and then rendered them immortal by making them cancerous.

The AstraZeneca, Cansino, Gamayela, Vaxart, LongComm and Upitt vaccines are manufactured in the human fetal cell line HEK293, and thus the final vaccine products will contain cellular debris and DNA fragments from the fetal HEK-293 cell line. Scientists harvested this cell line from the kidney of a female Dutch fetus legally aborted in 1973 and then immortalized the cells by rendering them cancerous.

Normal primary cells, which are unable to replicate indefinitely, ultimately die. Immortalized cell lines are derived from known malignant cancer cells such as those obtained from Henrietta Lacks (HeLa) or created in the laboratory by introducing viral oncogenes or chemical exposures capable of mutating normal primary cells into immortal tumor cells.

According to FDA’s “The Pink Sheet” dated Nov. 29, 1999, for two decades the agency has been acutely aware of the inherent risks of using immortalized cell lines for vaccine development. The FDA CBER Director Dr. Peter Patriarca, M.D. explained that continuous cell lines are used for their ability to self-propagate, making them an ideal substrate on which to grow viruses, “the worst thing we are concerned about is …  malignancy, because some of these continuous cells have the potential for growing tumors in laboratory animals.”

Patriarca further conceded that “the technology to make these vaccines actually exceeds the science and technology to understand how these vaccines work and to predict how they will work.” This dire “black box” conundrum that Patriarca described in 1999 is even more acute today with the urgent pressure to develop COVID vaccines before manufacturers have tested them in animals or subjected them to long-term safety studies.

We call vaccines “biologics” because vaccinologists have traditionally grown their antigens on biological substrates — usually animal tissue. Competing companies culture COVID vaccines on a variety of animal strata. The Merck and IAVA COVID vaccines are manufactured in vero monkey cells, and thus contain cellular debris and DNA fragments from vero monkeys in the final product. The Sanofi, GSK, and Novavax COVID jabs are manufactured in insect cells and thus contain insect cellular debris and DNA fragments in the final products.

Public health advocates criticize the use of animal tissues in vaccines due to risks that they carry endogenous viruses, microbes, parasites and lack safety testing. (Plague of Corruption, Mikovits 2020).The first use of human fetal cells in vaccines occurred around 60 years ago, but the practice is increasingly popular. It was always controversial. Immunologists long considered using cells from aborted human fetuses in vaccines to be a high-risk gambit; human DNA debris is much more likely to infiltrate cells in vaccinated individuals than insect or monkey DNA.

Researchers and regulatory agencies have worried for more than 50 years about the potential for injected DNA to cause cancer. According to Dr. Theresa Deisher, a research scientist, primitive (unmethylated) DNA chains from human fetuses have the ability to 1) activate immune receptors that could lead to autoimmune attacks in susceptible individuals who have genetic predispositions that cause their own DNA to be under-methylated, or 2) insert into cells where they could combine with host DNA and cause mutations.

Regulators have in the past predicted that the odds of that happening were less than 1 in a trillion. However, in early gene therapy trials this event did indeed occur in 4 of 9 boys, 1 of whom died from the leukemia the insertions caused.

“Researchers have long observed that when introduced DNA enters a cell, it chooses a region of the cell that gives it a survival advantage. These could be the regions that are most likely to produce long-living cancer cells,” Dr. Deisher told me. FDA has never made any effort to test the safety of this practice or to determine whether the epidemic of soft-tissue cancers is “vaccine-generation” children is related to the use of cancerous fetal cells in vaccines. Even worse, in 2002, FDA green-lighted vaccine companies to use cancerous tumor cells from adults in vaccines.

FDA as an arm of Big Pharma

Before reviewing the shocking transcript of the FDA meeting that approved this dubious practice, we need to understand the conflicts and corruption that pervade this rogue agency. If we are to ever develop safe, effective COVID vaccines, we need first to stop thinking of the FDA as a regulatory agency; it is an arm of the notoriously corrupt pharmaceutical industry.

According to a 2017 Emory University study entitled “Thick as Thieves? Big Pharma Wields Its Power with the Help of Government Regulation,” FDA bureaucrats act as “enablers, or perhaps worse still, [they are] complicit in questionable or ethically unsound activity as a result of being driven by self-serving motives ….” A 1992 law that allows drugmakers to buy fast-track approvals for new products from FDA has poured concrete on a regulatory dynamic already corrupted by all the ubiquitous mechanisms of “agency capture.”

Between 2000 and 2010, pharmaceutical companies paid the FDA $3.4 billion to gain rapid drug approvals. Today, Pharma companies underwrite three-quarters of FDA’s budget for scientific reviews (ProPublica) and fund nearly 50% of the FDA’s total annual budget through PDUFA fees. In exchange, the agency increasingly fast-tracks expensive drugs and vaccines with significant side effects and unproven health benefits.

No one at FDA wins kudos for slowing down those money flows. To the contrary, according to FDA’s own employees, drug company payments bias regulators, with “an inclination toward approval.”

According to Dr. Michael Carome, a former Health and Human Services (HHS) official and a director of the advocacy group Public Citizen, “Instead of a regulator and a regulated industry, we now have a partnership … That relationship has tilted [the FDA] away from a public health perspective to an industry friendly perspective.”

Corrupt vaccine approval panels

But as corrupt as FDA is, the internal panels — VRBAC — that approve new vaccines make the rest of the agency look like a Sunday church picnic.

When Dr. Fauci, Paul Offit, Peter Hotez and Bill Gates tell you that you needn’t worry because FDA is the “gold standard” for vaccine safety and that the ultimate licensing decision will be made by an “independent panel of experts,” they are talking about VRBPAC. But VRBPAC is far from “independent.” It is not even comprised exclusively of public officials. Instead, it is populated by outside “experts” who are almost all pharmaceutical industry insiders.



In 2003, following a 3-year investigation, the United States Congress’s House Oversight Committee found VRBAC was completely dominated by the vaccine industry.

According to findings of the congressional investigation, VRBAC’s “independent” vaccine panel members often share vaccine patents with the pharmaceutical companies whose products they are evaluating. They “own stock in those vaccine companies, receive payment from those companies for research and paid speeches. They occupy consulting lofty and powerful sinecures and accept payments to monitor vaccine trials and funding for their academic departments.”

The 2000-2003 U.S. House Government Reform Committee’s investigation of VRBPAC found that: (1) “The overwhelming majority of members, both voting members and consultants, have substantial ties to the pharmaceutical industry.” (2) “Conflict of interest rules employed by the FDA … have been weak, enforcement has been lax and committee members with substantial ties to pharmaceutical companies have been given waivers to participate in committee proceedings … In many cases, significant conflicts of interest are not deemed to be conflicts at all.”

Congressional investigators offered a typical example of the sort of financial entanglements that put VRBPAC under Pharma’s slavish control. That example was the December 12, 1997, VRBPAC meeting that approved Wyeth’s (now Pfizer’s) rotavirus vaccine, Rotashield.

The Congressional investigators detailed the committee’s cozy nepotism with vaccine makers.

“Examples of Conflicts of Interest:

    1. “For instance, 3 out of 5 FDA advisory committee (VRBPAC) members who voted to approve the rotavirus vaccine in December 1997 had financial ties to pharmaceutical companies that were developing different versions of the vaccine.
    2. “One out of five voting members’ employer had a $9,586,000 contract for a rotavirus vaccine.
    3. “One out of five voting members was the principal investigator for a Merck grant to develop a rotavirus vaccine.
    4. “One out of five voting members received approximately $1 million from vaccine manufacturers toward vaccine development.”

Congressional investigators concluded that, “Altogether, four out of the five committee members had conflicts of interest that required waivers, and their recommendation for approval of the vaccine was unanimous.”

Here’s what happened at the 2012 FDA meeting on fetal cells

HHS acknowledges that the FDA and Centers for Disease Control committees that contract and review new vaccines have historically not used “evidence-based medicine.” To illustrate what this means, one only need read (below) the astonishing transcript of the 2012 panel that first approved the use of adult cancer tumor cells in vaccines.

This transcript shows what the public is never supposed to see: the behind-the-scenes sausage-making of federal vaccine approvals. Here, you will read for yourself how the “independent,” “gold standard” panelists entrusted with protecting your children made monumentally consequential decisions, not on evidence-based science, but by rolling the dice and taking what they knew was a horrendously risky bet on public health

In any other realm, this transcript would be proof of negligent homicide. The sickening side-view of VRBAC’s deliberations reveals FDA’s “trusted experts” for what they are; sadistic boys in lab coats giddily discussing the removal of wings from flies. We are all lab rats in their high-risk population-wide experiment. At FDA’s vaccine division, that sort of reckless decision-making is routine.

In 2012, most live virus vaccines were from animal tissue and the idea of putting potentially cancerous tumor cells from adult “donors” in vaccines was still a daring and audacious gamble. That September, the FDA VRBPAC committee met to discuss this risky innovation. The transcript of that meeting — showing captive FDA officials considering a proposal by the pharma cabal to allow the use of human cancer cells (HeLa) to replace animal tissue in the manufacture of vaccines — is proof of reckless criminal conduct.

The HeLa cells are well known to cause cancer in animals, but Big Pharma wanted to lower production costs of vaccines and this method is cheaper and faster than using animal tissue for the cultivated media. The obvious question of whether such vaccines might induce cancer in recipients was on the top of the VRBPAC agenda. Health authorities and vaccine manufacturers blatantly acknowledged their uncertainty regarding the safety of vaccines made from HeLa cancer tumors as they voted to make a dangerous high-stakes gamble that would lower costs for vaccine makers

Unbelievably, FDA voted to allow pharmaceutical companies to produce vaccines using human cells without reviewing a single scientific study to determine if the outcome would be safe.

Before, I quoted some of the criminally reckless statements from the meeting directly. A more detailed account appears in this article.

This was a full meeting of FDA’s VRBPAC in 2012 to decide on the use of human tumor cell lines for the production of vaccines. I list these speakers and their titles at that time:

  • Dr. Philip Krause, Acting Deputy Director of OVRR (Office of Vaccine Research and Review) and FDA’s CBER (Center for Biologics Evaluation and Research). Also, Principal Investigator for Vaccine Safety: Virus Detection and Latency.
  • Dr. Doug Lowy, Director of the National Cancer Institute of the NIH.
  • Dr. Robert Daum, Chair of the VRBPAC.
  • Donald W. Jehn M.S., Designated Federal Officer for VRBPAC.
  • Keith Peden, PhD, Chief of LDNAV, DVP/OVRR/CBER.
  • Dr. Marion Gruber, Director of the FDA’s Office of Vaccines.
  • Dr. Nathanial Brady, a self-described clinician.
  • Dr. Pamela McInnes, a vaccine development expert and the Director of the Division of Extramural Research at the NIH’s National Institute of Dental and Craniofacial Research, and previously a Deputy Director under Anthony Fauci at the National Institute of Allergy and Infectious Diseases.
Pharma knew that their tumorigenic vaccines might cause tumors in recipients.

Dr. Philip Krause acknowledged the risks when he said: “We have really identified three major factors that could potentially convey risk from tumor-derived cells. And these include the cells themselves … and if they were tumor-derived cells then maybe they themselves could form tumors in a vaccine recipient.”

Government regulators acknowledged that tumor cell lines can cause tumors.

Dr. Doug Lowy acknowledged this when he said: “What I think is qualitatively different about the tumor cell lines is the fact that they can cause tumors.”

FDA officials knew that tumors might occur decades after vaccination.

Dr. James Cook acknowledged this when he commented: “But certainly, if you are going to address this question about tumor risk from vaccines made in tumor cell lines, it’s going to have to be a decade’s question.”

FDA openly acknowledged that its primary objective was not to assure public safety but to help vaccine manufacturers.

Dr. Robert Daum, the leader of the meeting, commented: “ …but we are here to consider the issues that we would like to advise the agency to consider in helping the company continue the manufacturing process, what should they be concerned about, what should they be watching for.”

FDA officials knew that they could not prove vaccine safety using test animals to assess oncogenicity.

Dr. Keith Peden acknowledged this fact when he said: “I’m not optimistic that we’re going to find animal models to assess oncogenicity of DNA. That’s why I’m feeling that maybe it’s the clearance aspect that we have to deal with, with respect to DNA.”

FDA officials deliberately terminated animal safety tests too early in order to conceal consequences.

Dr. Robert Daum acknowledged this fact when he said: “Are they watching these animals long enough? Should it be longer?”

Dr. Keith Peden acknowledged this fact when he said: “Is it relevant to safety that a cell forms a tumor after a year, a year-and-a-half?”

FDA decided to keep the tumor cell lines secret, because doctors and the public may be alarmed and say “Oh, my God!” if they knew the truth.

Dr. Nathanael Brady acknowledged this when he said: “How is this group (of vaccines) going to be able to be accepted by the consumers … As soon as you hear “a tumor-derived cell line,” how do you explain that, put the public at ease?”

Dr. Robert Daum further acknowledged these facts: “ …the practicing medical community and also the lay public. They are going to hear that we are recommending, or that the manufacturers are making, vaccines with tumorigenic cell lines and say, ‘Oh, my God,’ even if there’s no scientific basis to say, ‘Oh, my God.’”

FDA decided to use deceptive language to convince doctors and the public that the vaccines were safe even when they, themselves, were unconvinced of safety.

Dr. Philip Krause acknowledged this when he said: “… because it’s a discussion of how one communicates these issues and how the public will perceive them. But I’m not completely sure that we have a complete answer on the fundamental scientific question. So how can you communicate a scientific consensus that the product is safe unless we’re sure that you, the experts we are asking to advise us, are convinced that it’s safe?”

FDA decided to hide information about their use of tumor cells and omit it from package inserts.

Dr. Marion Gruber proposed this deception when he said: “The minute you describe something in the package insert in terms of potential clinical safety concerns, I think that really precludes using these cell substrates.”

Dr. James Cook agreed to the deception when he said: “When it gets right down to what’s in the vial and what the patient is going to ask me about, whether it’s safe, I’m not going to say, well, you know, HeLa cells kill nude mice.”

Dr. Robert Daum acknowledged the deception when he said: “I don’t know that our charge is to micromanage the package insert today. I think that’s a new discussion, with lots of issues that we haven’t really aired completely.”

Health authorities were skeptical about safety of the tumor lines, but they decided to subject the public to the risk, so that they could perform a global population-wide live human experiment.

Dr. Robert Daum agreed to conduct the mass human experiment with the following statement: “So I’m not sure that we can give a certainty there’s no risk — don’t worry about this … It’s sort of a brave new world. We’re all doing it together. But I think that you are doing a beautiful job.”

FDA officials opted to toss the dice, perform the population-wide human experiment, and learn about the risks as time goes by.

FDA officials even cast this experiment as a noble venture in the quest for scientific knowledge. Dr. Pamela McInnes made this stunning appeal to her colleagues: “… even though there are challenges [risks to humans] to using the new technologies, they have to be embraced and we have to continue to try to learn from them and struggle through that learning curve.”

In the end, FDA decided to take the risks. The leader of the committee says, “I’m a vaccine guy,” then urged his cronies to approve.

Dr. Robert Daum said: “I’m a vaccine guy. They are wonderful to prevent infectious diseases … I hope that I’m speaking for everybody when I say that’s the answer to your question. If not, please chime in now.”

The committee formally approves the method of making vaccines from human cancer tumors.

Dr. Robert Daum said: “To come back to the agency’s question of whether this committee believes it’s correct scientifically to go forward with the development of these vaccines, our answer is yes.”

Prior to voting to go forward, the committee made the following conclusions:
  • Making vaccines with cells that are directly derived from human cancer tumors is faster and cheaper than breeding animals for the culture media.
  • Millions of potentially cancer-causing vaccines will be produced.
  • The vaccines may possibly cause genetic mutations.
  • Millions of dollars will be made by vaccine promoters.
  • The health of millions of consumers may be jeopardized.
  • Information about how vaccines are made will be hidden from doctors and consumers.

This 2012 VRBPAC meeting perfectly illustrates the reckless, malevolent and murderous zeitgeist underlying the Pharma/HHS partnership. VRBPAC’s “devil-may-care” decision-making allowed pharmaceutical companies to use potentially cancerous fetal cells to make millions of vaccines.

Since that meeting, vaccines containing cancerous cells and DNA strands from aborted fetuses have become pervasive among the 72 doses of vaccines that FDA has approved, and CDC “recommends” for American children. Today, the vaccines for chickenpox, MMR, hepatitis A and shingles contain fetal DNA.

There is little chance of consequence to vaccine makers from making this reckless choice, and much potential benefit. The 1986 National Vaccine Injury Act makes pharmaceutical companies immune from negligence claims and from product defect lawsuits by injured plaintiffs. Since cancer takes years to develop, causation is virtually impossible for injured petitioners to prove in the Federal Vaccine Court where HHS is the defendant.

Furthermore, by the time a tumor develops, the three-year statute of limitations for the vaccine injury has long expired. Pharma is therefore recklessly and pathologically bold about putting carcinogens in vaccines.

Finally, it’s worth considering that cancer treatment drugs like Keytruda are among pharmaceutical companies’ largest profit makers. Precipitating a cancer epidemic in human populations only benefits vaccine makers’ bottom line.

Remember, these are the same companies and the same FDA regulators that brought us the opioid epidemic.




Warning: Anti-Fertility Shot

Warning: Anti-Fertility Shot

by Rosanne Lindsay, ND, Nature of Healing
December 7, 2020

 

A new experimental, genetically engineered, recombinant mRNA COVID vaccine is being released ‘at warp speed’. China biotech companies are promising millions of doses of COVID vaccines.  The United States paid billions to six other companies, including Pfizer pharmaceutical, which are ready to deploy their versions of the not-yet-FDA-approved shot.

Pfizer Warning Disclosed

In a December 2020 article in LifeNews.com, Pfizer pharmaceutical WARNED pregnant women not to use the COVID-19 mRNA vaccine due to fertility and breastfeeding risks. While this is important news for millions of women, Pfizer has not warned anyone that their study excluded two other groups: 1) those who had a previous diagnosis of COVID-19 disease, and those who are immunocompromised. Immunocompromised people fail to adequately to clear infections.  Those with an autoimmune disease create autoantibodies that attack their own tissues. They also fail to clear infections adequately. According to medical doctors, “both groups can create potentially life-threatening conditions.”

As of 2017, 50 million people, or 20% of the population have one or more autoimmune disease. Many people with autoimmune disease may not know that development of autoimmune disease is linked with exposure to aluminum adjuvants, which are found in vaccines.

If you are immunocompromised with an autoimmune disease, The American Autoimmune and Related Diseases Associations (AARDA) suggests you proceed with caution when it comes to the COVID shot. See their guidelines here for autoimmune conditions.

What if you want to get pregnant?

Is the shot worth the risks?

GARDASIL Recycle

On December 1, 2020, the ex-Pfizer head of respiratory research Dr. Michael Yeadon requested the European Union to halt the COVID vaccine, calling it female sterilization:

The vaccinations are expected to produce antibodies against spike proteins of SARS-CoV-2. However, spike proteins also contain syncytin-homologous proteins, which are essential for the formation of the placenta in mammals such as humans. It must be absolutely ruled out that a vaccine against SARS-CoV-2 could trigger an immune reaction against syncytin-1, as otherwise infertility of indefinite duration could result in vaccinated women.

The COVID vaccine follows in the wake of the last recombinant vaccine for the human papilloma virus (HPV).

In 2007, the HPV4, quadravalent, GARDASIL triple-shot series was introduced to girls ages 9-26, to prevent infertility. Then came HPV9 given as two or three shots. No one reported that Gardasil-9 contains more than double the toxic aluminum content of the original vaccine and has no fewer reported side effects.

After more than a decade of reviews, GARDASIL has proved to do exactly the opposite of what it claimed. For more, see my 2014 article Guard Against GARDASIL and a 2018 article by the Weston A. Price Foundation.

The deployment of the HPV GARDASIL vaccine worldwide resulted thousands of young women in the E.U. who suffered. In the U.S., over fifty-eight thousand adverse reactions—including four hundred twenty-seven deaths—have been reported after HPV vaccine injections. The primary adverse effect experienced by recipients was listed as Primary Ovarian Insufficiency (POI) resulting in premature menopause.

Infertility.

Reported in the medical journals, adolescent infertility is a facet of the Autoimmune/Inflammatory Syndrome Induced by Adjuvants.

An adolescent infertility shot that increases the risk of infertility and autoimmunity?

Imposter DNA

According to pathologist, Dr. Sin Hang Lee, well-known for using cutting-edge DNA sequencing for molecular diagnoses:

Once a segment of recombinant DNA is inserted into a human cell, the consequences are hard to predict. It may be in the cell temporarily or stay there forever, with or without causing a mutation. Now the host cell contains human DNA as well as genetically engineered viral DNA.

Under the Trojan Horse of a vaccine, imposter DNA can be injected and incorporated into your own DNA that manufacture proteins, aka autoantibodies, that attack your cells. Not only do autoantibodies lead to autoimmune diseases, but also to ADHD, seizures, autism, Alzheimer’s and Sudden Infant Death Syndrome (SIDS). All fall under the heading of Autoimmune/Inflammatory Syndrome Induced by Adjuvants. Adjuvants are aluminum-based neurotoxins of vaccines.

In 2016, Dr. Lee sent an open letter of complaint to the World Health Organization’s Global Advisory Committee on Vaccine Safety citing lack of safety data on the vaccine and lack of credibility. But global authorities pay no attention to deaths and injuries caused by vaccine products since vaccine makers are not held accountable for any damages from their products under Bubble Indemnity.

The medical narrative uses fear and contradiction to confuse. They suggest that a virus called HPV “makes it more difficult for a woman to conceive and remain pregnant.” Yet in the next sentence they disclose “However, it is important to remember that most cases of HPV clear up without any need for treatment.” In the fine print, scientists also disclose that no study suggests that HPV contributes to infertility.

The media promoted the experimental HPV jab, not only as a prevention to infertility, but also as a “cure-all” for cervical cancer and genital warts.

Scientists admit that the immune system clear up infections on its own, without treatment. If you consider that clue, you might say goodbye to the germ theory. Under The Terrain Theory, viruses are called exosomes, like enzymes, created within your own cells to cleanse the cells of toxins, a self-cleaning service by your cells. So, while the Germ Theory of disease paints a virus as an enemy, the Terrain Theory of disease welcomes a virus as a friend.  The deception of virology and vaccines says that viruses are alive and contagious when they are not:

The entirety of virology and vaccine science is predicated on one thing—that viruses are infectious agents that cause disease.
Without this theory, vaccines would not be ‘effective’ or ‘work’ in the minds of the people.
Without the virus theory, vaccines would crumble like a house of cards.

The Mandate Strategy

The HPV recombinant vaccine mandate was part of a strategy to coerce compliance with vaccines that genetically modify human DNA. In 2007, both Merck Pharmaceutical and Texas Governor Rick Perry, pushed an HPV vaccine mandate  for young girls, ages 9-14. Parents had to consent. However, the editor of JAMA opposed mandating vaccinating girls against the virus.

Note: there will always be two opposing scientific narratives to keep people confused about their inherent right to refuse. Science is a distraction in the health freedom equation.

The HPV vaccine mandate failed. Then, in 2018, scientists pushed the vaccine on boys, suggesting that the presence of HPV in contaminated sperm negatively affects pregnancy outcomes. The CDC claimed that it provides long-lasting protection against penile and anal cancer. But what happens after the vaccine efficacy wanes after 3-5 years?

When women face only a 0.6 percent risk of cervical cancer and men face a 0.2 percent risk of rare anal and penile cancers, is it logical to continue to use a vaccine with so many complications?

Since the 2007 GARDASIL shot first rolled out, negative effects have continued in both boys and girls. A recent July 2020 study in Scientific Reports titled, Human papillomavirus vaccine-associated premature ovarian insufficiency and related adverse events: data mining of Vaccine Adverse Event Reporting System concluded:

We detected disproportionate reports of premature ovarian insufficiency (POI) and related events, including amenorrhea, menstruation irregular, FSH increased, and premature menopause, following human papillomavirus (HPV) vaccine from FDA Vaccine Adverse Event Reporting System (VAERS).

2018 Indian Journal of Medical Ethics study titled “Increased incidence of cervical cancer in Sweden: Possible link with HPV vaccination,” was later retracted.

An anti-cancer shot that increases the risk of cancer?

Ironically, HPV vaccines have injured and killed far more children than ever would have gone on to develop HPV-associated cancers without the vaccine. Before the ‘warp speed’ deployment of the next experimental, recombinant shot, it might be wise to assess the damage from the consequences of the last one.

HPV Vaccine Damage Report

May 2007 editorial in the New England Journal of Medicine questioned the vaccine’s “overall vaccine effectiveness, duration of protection, and adverse effects that may emerge over time,” as the clinical trials did not provide these answers.

VAERS, continues to receive reports of young girls experiencing serious reactions to GARDASIL Adverse reactions include unconsciousness, seizures and facial paralysis, Bells Palsy, Guillain Barre syndrome, speech and vision problems, arthritis, and lupus, and death, after being injected.

Public Interest Group, Judicial Watch, reported in May 11, 2007, that the VAERS data base showed 1,637 adverse reaction reports. Of 42 women who were vaccinated with GARDASIL while pregnant, 18 experienced complications, ranging from miscarriages to fetal abnormalities. As of Dec. 13, 2013, there were a total of 29,918 vaccine reaction reports made to the VAERS associated with GARDASIL vaccinations, including 140 deaths.

In 2011, the Institute of Medicine (IOM) produced a report, Adverse Effects of Vaccines: Evidence and Causality, concluding that “evidence convincingly supports a causal relationship between HPV vaccine and syncope (fainting), and anaphylaxis.”

In a December 2012 study in the journal Advances in Bioscience and Biotechnology, Dr. Lee confirmed the presence of vaccine DNA fragments (HPV-16 L1) in the postmortem blood of a girl who had died shortly after receiving the GARDASIL vaccine, noting the vaccine has the ability to provoke an exaggerated immune response. He also pointed out that the rate of anaphylaxis in girls receiving GARDASIL is five to 20 times higher than any other school-based vaccination program.

In a 2014 study from Keele University in England, Dr. Christopher Exley, examined sixty-two semen samples and found “unequivocal evidence” of high concentrations of aluminum, especially in the semen of men with low sperm counts.

A review published in the 2014 Autoimmunity Reviews linked the HPV vaccine to autoimmunity:

Along with the introduction of the HPV vaccines, several cases of onset or exacerbations of autoimmune diseases following the vaccine shot have been reported in the literature and pharmacovigilance databases, triggering concerns about its safety.

A 2015 study at the University of Texas showed that young women, ages 20-26, who received the four-strain GARDASIL vaccine were more likely than non-HPV-vaccinated women to be infected with high-risk nonvaccine strains of HPV ten years later. In other words, there is a greater risk of infection in those who take the vaccine.

In the 2018 Journal Pediatrics, a Vaccine Safety Datalink study titled, “Primary Ovarian Insufficiency and Adolescent Vaccination,” correlated ovarian failure with vaccinations, including HPV vaccines.

The March 24, 2020 British Medical Journal titled “Ongoing inadequacy of quadrivalent HPV vaccine safety studies” concluded, “Cochrane could not exclude an increased risk of HPV vaccine mortality “and “medical journals are at risk of becoming arms of the pharmaceutical industry highlights an increased scientific need for alert and active critique of industry-funded trials. [

A June 2018 study (retracted) in the Journal of Toxicology and Environmental Health analyzed a database of more than eight million American women and found a 25 percent lowered probability of pregnancy associated with HPV vaccination.

As of December 2019, data from the CDC shows that more than one in eight American women—12 percent—have trouble conceiving and bearing a child.

Based on this review, will the COVID19 shot increase the risk for respiratory distress, infertility, autoimmunity and cancer all in one?

Trust Your Innate Immune System

If you are a woman of child-bearing age, do you want the choice to be a mother?

If you are pregnant or nursing, congratulations. Avoid the the two-shot COVID-19 mRNA Vaccine if you want to have more children. According to a UK government document for medical professionals states that there is little data about the risks of the vaccine thus far, and animal reproductive toxicity studies are not finished. Therefore, the Pfizer vaccine, BNT162b2, “is not recommended during pregnancy.”

Pregnant or not, know you always have a choice. You can choose to trust a vaccine maker who is not liable, or reliable, because they do not stand behind their products. Or you can trust your gut, the center of your innate immune system, the defense system you were born with.

Your immune system is designed to work in balance with nature, under the laws of nature, or Holism. This innate system is balanced between two poles: 1) cellular or T cell-mediated immunity, and 2) humoral or B cell-mediated immunity, and they have a reciprocal relationship. When one is artificially stimulated, the other is suppressed.

When viruses are injected into the body, an imbalance occurs—only B cells are activated to create antibodies. Killer T cells are subsequently inhibited, and an engineered virus can temporarily inactivate killer T cells. Dr. Rebecca Carley, M.D. writes, “The ‘prevention’ of a disease via vaccination is, in reality, an inability to expel organisms due to the suppression of the cell-mediated response. Thus, rather than preventing disease, the disease is actually prevented from ever being resolved.”

Holism explains that when people are exposed to a virus, not everyone gets sick. Researchers at the University of Michigan (U of M) showed that when injected with infectious viral agents, a strong immune system and infectious disease could not co-exist. That’s because the cells of your immune system determines whether a virus manifests or not.

When it comes to COVID or any condition, why inject a virus which medical experts claim causes disease? If it is well established that autoimmunity is induced by aluminum adjuvants, then is this shot safe for anyone?

 


Rosanne Lindsay is a Naturopath, writer, earth keeper, health freedom advocate and author of the books The Nature of Healing, Heal the Body, Heal the Planet and  Free Your Voice, Heal Your Thyroid, Reverse Thyroid Disease Naturally.

Rosanne Lindsay is available for consultation through Turtle Island Network.  Subscribe to her blog at natureofhealing.org.

 

Connect with Rosanne Lindsay, ND




Dr. Vernon Coleman: Vital Information About the Covid-19 Vaccine

Vital Information about the Covid 19-Vaccine

by Dr. Vernon Coleman
December 4, 2020

 



Original video available at Vernon Coleman’s Brand New Tube channel.

[As a service to protect truth from censorship & to share widely, mirrored copies of this video are available at Truth Comes to Light BitChute, Brighteon, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]

Transcript:

Imagine this. A man and a woman get into a car. The woman sits in the driving seat. The man in the passenger seat. The woman is taking her driving test and the man beside her is the examiner. The woman is a terrible driver and no one thinks she will pass the test.

Before she starts the car the woman unfastens her handbag, removes her purse and takes out £1,000 in nice new banknotes. She then turns to the driving examiner.

`I know you and your wife both need a nice holiday,’ she says, handing over the money. `This has nothing to do with the driving test I’m about to take but I’d like you have this.’

`Well, thank you, very much,’ says the driving examiner. `Now, let’s see how you get on with your driving test, shall we?’

You might think a trifle unlikely.

But listen to this.

The Bill and Melinda Gates Foundation has a chunky sized investment in the drug company Pfizer which is making the new vaccine which has just been approved for covid-19 in the UK.

The MHRA in the UK is the first regulator in the world to approve the vaccine. It’s fair to say that other countries are possibly a bit puzzled. I don’t think anyone envies Britain for having the fastest regulator in the world. In the US, Dr Fauci, originally said the UK regulators had rushed their approval. But, predictably, he later apologised for saying that. What a surprise that was to us all.

But in 2017 the Bill and Melinda Gates Foundation entered into what I can only call a financial arrangement with the MHRA – the bit of the UK government which regulates medicines and makes sure that they are safe. (MHRA stands for the Medicines and Healthcare Products Regulatory Agency).

Bill and Melinda’s Foundation handed over £980,000 to the MHRA.

So bear with me if I go over this again.

First, the Bill and Melinda Gates Foundation makes a big investment in Pfizer.

Second, the Bill and Melinda Gates Foundation hands over £980,000 and the MHRA smiles sweetly and says thank you very much.

Third, the MHRA is the first agency in the world to approve the new Pfizer vaccine. It is, I suspect, the fastest ever approval of a vaccine.

Even if this tripartite relationship is entirely innocent it should never have happened. What is yet another Government agency doing accepting money from Gates? It was Gates who said that if they were very good at vaccinating people they could reduce the population considerably.

And Pifzer?

Well, to be honest with you, Pfizer’s record isn’t anything you would want to boast about. If you worked there you’d keep quiet about it I think and say you worked for the tax people or robbed banks for living.

So, for example, in the UK, Pfizer was fined £84.2 million for overcharging the NHS by 2,600% and in the US Pfizer was hit with a $2.3 billion fine for mis-promoting medicines and paying kickbacks to doctors. At the time I think the $2.3 billion fine was one of the biggest fines for fraud in American history. It might still be for all I know.

The MHRA should be closed down immediately.

And how did my imaginary driving test student get on?

Oh, to everyone’s surprise she passed her test. She hit a bus, ran over two old ladies and collided with a lamppost when she tried to park. But she passed.

And so this is Britain today.

I have been writing about doctors and drug companies for half a century. My first book on drugs and drug companies was called `The Medicine Men’ and it was published in 1975. I can honestly say I have never come across anything quite so disgraceful, so blatant as the MHRA, Bill Gates and Pfizer link.

And no one cares.

Have you heard about this on the BBC?

Have MPs been shouting about it?

Have the papers run this story on their front pages?

I despair. I really do.

Meanwhile, the confusion goes on and on.

Matt Hancock’s chum and co-author, who is now in charge of vaccinations in the UK or is it just England or maybe just Stratford-upon-Avon, suggested that people who don’t have the covid-19 vaccination might not be allowed to enter cinemas or watch football matches.

I wasn’t surprised. They were always going to say that.

And then senior ministers seemed to change their mind and overrule him. But I rather bet that people who have the vaccine will be given some sort of certificate. After all the EU has been planning a vaccination passport since 2018.

The American government has a clinical trial under way which is testing messages to see which ones are most likely to persuade people that they should have the vaccination.

If you want to get your freedom back,’ then accept the vaccine.’

`If you want to keep your job,’ then accept the vaccine.’

That sort of thing. All devised by psychologists to manipulate, blackmail and coerce. And all for a vaccine which experts around the world agree is for an infection which is no more lethal than the ordinary, annual flu. You can see why the trickery is necessary.

Almost every survey I have seen suggests that most people don’t want the vaccine. Even many health professionals don’t want it. My friend Dr Colin Barron reported that even a great chunk of GPs said they wouldn’t have the vaccine – and they’re making over £12 a jab for giving it.

Of course, if governments everywhere wanted to persuade people to have the vaccine they could be a little more open about the advantages and disadvantages: the benefits and the risks.

It is normal in medicine for doctors to tell patients about all the side effects which may be associated with the treatment they are having.

Indeed, it isn’t just normal, it’s compulsory.

If you go into hospital to have an operation they’ll list all the possible things that can go wrong.

If you are given medication then they’ll tell you about the hazards. Or they should. It’s called informed consent.

There is only one exception: vaccines.

There is no such thing as `informed consent’ about vaccines because doctors aren’t allowed to question vaccines and vaccination in public.

Since anyone who questions the safety or efficacy of vaccines is automatically defined as an anti-vaxxer they can hardly expect doctors to tell patients about the risks. If they did then every doctor would automatically be an anti-vaxxer and be demonised.

You don’t have to be spreading rumours about vaccines to be classified as a dangerous anti-vaxxer.

Some are asking if the first dose of the vaccine will be merely a placebo – to encourage everyone to believe the vaccine is safe. I’m not surprised people are asking that.

After all, lots of dirty things happen in the world of vaccines. Back in 2009, Time magazine reported that Germany had been accused of offering a flu vaccine made by one company, and believed to have fewer side effects, to politicians, civil servants and soldiers and another, potentially riskier vaccine to everyone else.

The riskier vaccine was called Pandemrix. And I dealt with that in my book `Covid 19: The Greatest Hoax of the Century’ – which was banned almost everywhere but which is now available free as a pdf on my website www.vernoncoleman.com and is also free on the Light Paper website – thelightpaper.co.uk

Any doctor who questions the efficacy of a vaccine is officially an anti-vaxxer. If the alleged virus has never been isolated and identified how have they managed to make a vaccine? Why is the vaccine said to be better than natural immunity? Why will people need more than one dose? Why will they need it every year? It’s illegal to ask the questions so there are no answers.

The social media channels such as ScrewYouTube don’t differentiate between loonies suggesting that vaccines will make your hands drop off and turn you bright blue and experienced physicians asking for more information about vaccines.

Everyone asking for information about vaccines is officially an anti-vaxxer – and will be silenced.

The British Army is now concentrating on removing material from the internet if it questions vaccines and vaccination.

I doubt if the soldiers doing this work are qualified doctors – they aren’t expected to judge between serious, professional questions and wild accusations.

They just take down everything.

ScrewYouTube does the same, of course.

Any video which questions vaccine safety, reports acknowledged vaccine problems or criticises drug companies which make vaccines will be deleted.

No questions asked. No chance to defend.

Simple, rapid execution.

The authorities seem to me to have created a problem, the alleged covid-19 epidemic, and they have created a solution – a vaccine.

And yet the list of questions which need to be asked grows longer every day.

I predicted some time ago that there could be infertility problems with the vaccine, and on 3rd December Richie Allen broadcast details of government guidelines which suggested a huge – but not entirely unexpected – cover up.

Richie revealed that although health care professions are warned that it is unknown whether the vaccine has an impact on infertility this warning was not included in the information for those having the vaccine. Maybe there will be an infertility problem and it won’t be apparent for another five or ten years when a few thousand nurses and doctors find they can’t get pregnant. Bill Gates has a certain amount of history in this area.

Medical journal articles have suggested that there are a lot of questions still unanswered.

It’s difficult to know precisely what has been tested, of course, because there is a great deal of secrecy about the trials.

A vaccine should stop serious illness developing and it should interfere with the transmission of a disease and it should be safe.

Do any of the covid-19 vaccines do all or any of these?

The mysteries seem endless.

Will the vaccine really be safe for 80-year-olds? Has it been tested on 80-year-olds? Back in March 2020 I warned that one of the aims of this whole hoax was to get rid of old people. Is this what is going to happen now? Back in March I also warned that another aim was to introduce mandatory vaccinations.

It is said that 100% of those who had two doses of Moderna’s mRNA vaccine had what are called systemic adverse events. Not nice.

And 50% of those who had the Pfizer vaccine were said to be ill.

The Astra Zeneca trial was similar.

And The Lancet reported that there was a possibility that people who had one of the vaccines might have an increased risk of developing an HIV infection.

When testing new drugs, companies usually test against a placebo. Half the patients in a trial get the new drug and half get a sugar pill.

But in their trial it seems that Astra Zeneca tested their new covid-19 vaccine against a meningitis vaccine which is known to produce significant adverse effects.

Why would they do this?

Well, at the risks of upsetting the 77th Brigade, could it be because this would enable them to argue that their vaccine was safer than the placebo?

Is that entirely fair? I doubt if I am the only doctor to think it isn’t.

Even the Financial Times seemed upset by Astra Zeneca. In an article headlined, `Doubts raised over Astra Zeneca Oxford Vaccine Data’ the FT reported that there had been a mistake in the dosage given and that all the people testing the vaccine had been under 55 years of age.

By questioning the vaccine has the FT has become an anti-vaxxer newspaper? Will their website will now be taken down?

The questions keep on coming I’m afraid.

The head of `Operation Warp Speed’ in the USA, who is helping to get vaccines ready for use, is apparently a former GSK executive which seems to me to be a tad incestuous. Mind you, the Chief Scientific Officer in the UK is a former GSK executive.

What else can’t I tell you?

Well, it seems that a little quiet scepticism might not be entirely unfair. At least 66 fully tested and approved vaccines in the US have, over the years, been discontinued – largely for safety reasons. And billions of dollars have been paid in compensation to patients injured by vaccines – or paid to their relatives when patients died or were very severely injured. The UK Government has its standard, miserly £120,000 fee for vaccine damaged patients. And that is paid by taxpayers not drug companies.

What steps is the MHRA taking to ensure that any side effects are properly and speedily recorded?

Why did the drug companies insist on being given indemnity if their vaccines cause no problems? No other companies are indemnified if they produce dangerous products. Well, Bill Gates insisted on indemnity being given. The UK Government has, I think, finally agreed to give its standard £120,000 vaccine damage fee to anyone with severe side effects. But try living on £120,000 if you’re paralysed for life.

Still, there is one bright thought I can share with you.

The vaccine companies want their products to be given emergency approval. This will enable the vaccines to be brought out quickly – by accepting a lower standard of effectiveness and safety.

But when a vaccine is brought out using Emergency Use Authorisation the States in America are banned I believe from mandating the vaccine. They can’t force people to take it.

And a full licence, which would allow mandatory vaccines, will or should take years to acquire.

So here’s a thought: will it be legal for individual companies, schools and so on to insist that people have the vaccination?

And although the drug companies and doctors have been given legal immunity – they can’t be sued if their product is dangerous – does that immunity stretch to company bosses and teachers demanding that you have a vaccine?

One thing is for certain: if someone tries to force you to have a vaccine then it would be wise to insist that the boss signs and dates a letter confirming that he or she is forcing you to be vaccinated and that he or she takes responsibility for any health problems which ensue.

I wonder how many bosses would risk that.

Finally, don’t try bribing your driving instructor.

You could probably go to prison for that.

Only governments and billionaires can get away with that sort of behaviour scot free.


Copyright Vernon Coleman December 4th 2020

For the background to vaccines and vaccination, Vernon Coleman’s book “Anyone who tells you vaccines are safe and effective is lying – here’s the proof is available on Amazon as a paperback and an eBook.




At This Point, Are Americans Anything More Than Lab Animals?

At This Point, Are Americans Anything More Than Lab Animals?

by Gary D. Barnett, GaryDBarnett.com
December 9, 2020

 

“We slow the progress of science today for all sorts of ethical reasons. Biomedicine could advance much faster if we abolished our rules on human experimentation in clinical trials, as Nazi researchers did.” ~ Paul Nitze

The idea of brutal experimentation on animals has always been justified by claiming that it is necessary in order to benefit the health or mental well being of humans. This propagandist thinking could and would lead to a public acceptance of experimenting and torture of living things in the false name of human progress. But it was also meant to condition man to accept harm to one species in order to better his own. It stands to reason that once this mindset was in place, it could be argued that human experimentation could enhance that ‘progress’ much further, thereby becoming a necessary evil that could be seen as beneficial, especially if it began with psychological experimentation, and not physical. Now that the psyche and body are in many cases being seen as one and the same, why not use medical testing of some humans so as to benefit the collective? In this scenario, the individual would be destroyed in favor of the group, and this could easily lead to sacrificing some for the good of all. The result of this progression would be that we are all lab animals now.

In this era of the fraudulent coronavirus ‘pandemic,’ most are well on their way to becoming a nation of mindless drones that will be accepting of human experimentation. This is in fact already happening, but it seems that it will get much worse very soon. Fear can breed aggression, but considering the herd mentality of the human species, it is much more likely to breed passivity and compliance, both very detrimental to survival in what could be considered any normal way of life. It is not that this government and its controllers have not used its citizens and others for these purposes in the past, but today it is becoming rampant, and is even out in the open concerning current policies in place.

Most all that is now being mandated by the political class is based on experimentation. That experimentation is predicated on compliance testing, this regardless of the gross harm caused. You see, when experimenting with the human animal, it is first necessary to gauge the psyche of the average person in order to know how far the experiment can advance. Because of this, it is crucial to perform psychological experimentation prior to physical experimentation. This of course is not necessary with animals, but is vital with ‘reasoning’ humans. With mass compliance, it becomes evident to the ruling sector of society that the people are prepared to become guinea pigs, and therefore are ripe for abuse. These lockdowns, distancing rules, mask wearing, voluntary business closings, virus testing, and restrictions to liberty at every level, are simply tests to see if the people are willing to follow ludicrous and dangerous instructions in order to gain some sort of false safety due only to pre-planned government propaganda. It has been obvious that Americans in large part have been willing to do absolutely anything they were told to do, including allowing their older family members to be psychologically tortured, and effectively murdered, due to forced isolation by the state.

The ultimate goal of the state here is to first destroy the human spirit, leaving an empty mind and a blank slate so that the people at large are ready and willing to become the test subjects for their claimed masters. The day of the first significant physical experiment on this population is fast approaching, and at this time seems imminent. That experiment will rival many of the heinous and torturous ‘scientific’ persecutions of the past, but will be unique in that it will be made to seem voluntary instead of being done through incarceration and brute force. But there is a sinister aspect of this feigned voluntarism that exposes a heinous psychological manipulation.

I am speaking here of course of the coming poisonous ‘Covid-19’ vaccination. The contradiction and foretelling of doom is obvious, so why are so many already willing to be used as lab animals? The first sign of great danger lies in the fact that the state has exempted the pharmaceutical companies developing these experimental toxins from all liability. The state with your money is also paying for the development of these virulent injections, while allowing unlimited profit to its partners in crime. In addition, the government is claiming to be liable, but that is a lie, as government has nothing, and produces nothing; it only steals from those that do. So each and every citizen guinea pig taking this deadly and experimental vaccine is personally liable for any and all harm. What this means is that vaccine manufacturers, deliverers, and the government have zero risk, while the people retain all the physical, mental, medical, and financial liability. This is a true government coup d’état, in that the human lab animals take all the risk, contract all the sickness, disease and even face death, and also pay for all the damages.

While the political class will crow loudly about this not being mandatory, they will at the same time threaten every single individual that does not bow down to the state and take this vaccine. Those threats will be brutal, and meant to destroy any that do not comply. So this vaccine will really be mandated in that those that disobey will be abused, and attempts by the government to force consent will be completely inhumane. The ability to get daily necessities including food will be eliminated, as will most all travel, working and supporting family without an immunization pass, gaining medical care, access to any service, all public entertainment and activities, and most anything vital to life. Does this sound voluntary to you?

But this experimentation will not end here, but will also continue as long as the people allow it to continue. There will be new experimental vaccines, new updated injections, injectable nanoparticles, chips, property confiscation and redistribution, RNA and DNA experimentation, universal basic income, governmental digital money, tracking devices, and many other intrusions said to be necessary for any citizen wanting to be able to move about or function in any ‘new normal’ manner. So long as the people comply with these orders, the list of demands by the state will be innumerable.

We are all facing one giant experiment where the powerful controlling ‘elites’ and their pawns in government are the mad scientists, and the common masses are the lab animal test subjects.

There is only one answer to this madness: Disobey every government order and be prepared to defend at all costs your life, your family, your property, and your freedom!

“The enrichment center would like to announce a new employee initiative of forced voluntary participation.

If any Aperture Science employee would like to opt out of this new voluntary testing program, please remember; science rhymes with compliance.

Ted Kosmatka, Portal 2: Lab Rat

Source links:

Herehere, here, and here.

The Best of Gary D. Barnett




Doctors & Medical Experts Worldwide Warn Humanity Against Taking the COVID19 Vaccine

Doctors & Medical Experts Worldwide Warn Humanity Against Taking the COVID19 Vaccine

by World Doctors Alliance
December 7, 2020

 



Ask The Experts : Covid19 Vaccines

Original video is available at World Doctors Alliance Brand New Tube channel.

  1. Dr. Andrew Kaufman, Medical Doctor & Forensic Psychiatrist from the USA
  2. Dr. Hilde de Smet, Medical Doctor from Belgium
  3. Dr. Nils R. Fosse, Medical Doctor from Norway
  4. Dr. Elizabeth Evans, Medical Doctor from the UK
  5. Dr. Mohammad Adil, Medical Doctor from the UK
  6. Dr. Vernon Coleman, General Practioner from the UK
  7. Prof. Dolores Cahill, Molecular Biologist and Immunologist from Ireland
  8. Dr. R. Zac Cox, Holistic Dentist & Homeopath from the UK
  9. Dr. Anna Forbes, Medical Doctor from the UK
  10. Dr. Ralf ER Sundberg, Medical Doctor from Sweden
  11. Dr. Johan Denis, Medical Doctor & Homeopath from Belgium
  12. Dr. Daniel Cullum, Chiropractic Physician from the USA
  13. Moritz von der Borch, Medical Journalist from Germany
  14. Dr. Anne Fierlafijn, Medical Doctor from Belgium
  15. Dr. Tom Cowan, Medical Doctor from the USA
  16. Dr. Kevin P. Corbett, Retired Nurse & Health Scientist from the UK
  17. Dr. Carrie Madej, Medical Doctor from the USA
  18. Dr. Barre LandoPhysician from the USA
  19. Kate Shemirani, Natural Nurse from the UK
  20. Sandy Lunoe, Pharmacist from Norway
  21. Boris Dragin, Licensed Acupuncturist from Sweden
  22. Dr. Piotr Rubas, Medical Doctor from Poland
  23. Dr. Natalia Prego Cancelo, Medical Doctor from Spain
  24. Dr. Rashid Buttar, Medical Doctor from the USA
  25. Dr. Nour De San, Medical Doctor from Belgium
  26. Dr. Kelly Brogan, Medical Doctor from the USA
  27. Prof. Konstantin Pavlidis, Metaphysicist from the UK
  28. Dr. Sherri Tenpenny, Medical Doctor from the USA
  29. Senta Depuydt, Journalist from Belgium
  30. Dr. Heiko Santelmann, Medical Doctor from Germany
  31. Dr. Margareta Griesz-Brisson, Neurologist from Germany
  32. Dr. Mikael Nordfors, Medical Doctor from Sweden
  33. Dr. Elke F. de Klerk, Medical Doctor from Holland

Corman-Drosten review of PCR test

[As a service to protect truth from censorship & to share widely, mirrored copies of this video are available at Truth Comes to Light BitChute, Brighteon, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]

 




Call to Action: Join RFK, Jr. and Children’s Health Defense in Urging the FDA to Slow Down the COVID-19 Vaccine Approval Process

Call to Action: Join RFK, Jr. and Children’s Health Defense in Urging the FDA to Slow Down the COVID-19 Vaccine Approval Process

by Children’s Health Defense
December 7, 2020

 

On December 4, Robert F. Kennedy, Jr. sent a letter to Peter Marks, Director of the Center for Biologics Evaluation and Research’s (CBER), on behalf of Children’s Health Defense (CHD) asking the Food and Drug Administration (FDA) to take a cautious approach in approving COVID-19 vaccines that have been developed at “warp speed.” Considering that almost $4.5 billion has been paid out to vaccine injured individuals from vaccines developed in traditional timelines, caution, and concern for human safety should be the FDA’s top priority in the approval process.

This coming Thursday, December 10, CBER’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) will meet in open session to discuss Emergency Use Authorization (EUA) of the Pfizer-BioNTech COVID-19 vaccine for the prevention of COVID-19 in individuals 16 years of age and older. CHD asks that you take the following steps to urge VRBPAC to make safety the chief concern in its considerations:

  1. Send RFK, Jr.’s letter to CBER Director Peter Marks to both Marks and Senator Ron Johnson of Wisconsin, chair of the Senate Homeland Security and Governmental Affairs Committee who has expressed similar COVID vaccine safety concerns.
  2. Send the letter below to your representatives in the House and Senate letting them know that you support Mr. Kennedy’s call for caution in making decisions regarding emergency use authorization of Pfizer’s COVID vaccine as well as any other COVID vaccine in development.

With the VRBPAC meeting coming up so quickly, the time to act is now.

Link here to Robert F. Kennedy, Jr.’s letter
and easy fill-in form for sending.

 




Boom: Florida Forcing Labs to Report Number of PCR Test Cycles—Game Changer

Boom: Florida Forcing Labs to Report Number of PCR Test Cycles—Game Changer
If the governor of Florida handles this breakthrough correctly, it could be the beginning of the end for one widespread piece of COVID test fakery…
And the beginning of the end of “rising case numbers”

by Jon Rappoport, No More Fake News
December 8, 2020

 

As I’ve reported, COVID testing labs never tell doctors or patients how the PCR test is run. [1]

This means the number of cycles is a secret.

A cycle is a step up in amplification of the tissue sample taken from the patient.

As even Tony Fauci has asserted, tests run at 35 cycles or above are useless. [1] [2] They’re also misleading. The results tend to be positive, meaning the patient is “infected with the virus.” But this is false.

However, as I’ve also reported, the CDC and the FDA recommend that the test should be run at up to 40 cycles. [1] [3] This is a direct hustle. It ensures false positives and higher COVID case numbers—used as justification for lockdowns.

Now, the state of Florida is doing something unheard of. It’s demanding that labs report the “cycle threshold” for every test they run.

Here is the relevant wording in a release from the Florida governor, Ron DeSantis, and the state Department of Health, dated December 3, 2020 [4]:

“Cycle threshold (CT) values and their reference ranges, as applicable, must be reported by laboratories to FDOH via electronic laboratory reporting or by fax immediately.”

“If your laboratory is not currently reporting CT values and their reference ranges, the lab should begin reporting this information to FDOH within seven days of the date of this memorandum.”

We can assume there is only one reason for this order. The Florida governor and the Department of Health are aware that tests run at 35 cycles or higher are useless and misleading, and they want to stop this crime.

Imagine what happens if the trend of “new COVID cases” in Florida soon takes a sudden dip and keeps on falling—because labs are finally telling the truth. Because their deceptive test results are being rejected. The con will be exposed.

And imagine other states following Florida’s example.

I have a few concerns. The term “cycle threshold” is taken to be more or less synonymous with “number of cycles.” But I would prefer Florida simply say: “All labs must report the number of cycles for each PCR test they run.” For me, that would be clearer.

And then, down in the Florida memo, we have this: “If your laboratory is unable to report CT values and their reference ranges, please fill out the brief questionnaire attached to this memorandum and submit by facsimile to the FDOH’s Bureau of Epidemiology confidential fax line…” [the link to the questionnaire is in [4]]

Unable to report? Why would any lab be unable?

The questionnaire offers two bizarre possibilities. The first: “Although the qualitative result is generated based on a CT value, the assay/instrument does not provide the user [the lab] with the actual CT value—it only provides the qualitative result.”

What?? This indicates the lab’s PCR equipment is internally pre-programmed to run the test at a certain number of cycles, and the lab doesn’t know what that number is, can’t find out, and can’t demand the equipment manufacturer disclose that vital piece of information. ABSURD. We’re dealing with a state secret?

The second item in the questionnaire for labs: “The laboratory does not have a separate mechanism to report the CT value to FDOH [Florida Dept. of Health] since the CT value does not get reported to the submitting provider.”

No mechanism for reporting? SET ONE UP. Email, fax, pencil and paper, carrier pigeon. Also ABSURD.

As always, the devil is in the details. I’m sure many labs will try to avoid reporting. They don’t want to be exposed as the charlatans they are.

Memo to Florida Governor DeSantis: Don’t let the labs weasel out of this one. Don’t let them give you excuses. Don’t let them off the hook. Failure to report true facts during a public health crisis is felony. Charge a few labs, drag them into court. Put fear of prosecution into state labs. You’re on the right track. You’ve made a major breakthrough. You see the con at work. You don’t want your state to be pressured into lockdowns based on fake case numbers derived from deceptive tests. Now make sure your enforcement personnel crack down on reluctant labs. Go the distance. If labs have equipment pre-set for the number of cycles, and they don’t know how to get inside the equipment to find that number, bring in pros who will do the job for them. I believe you’ll uncover a major scandal. Much of that equipment will be pre-set for 40 cycles. Keep updating the public on what you discover. Blow this crime wide open. Keep a very close eye on your public health officials. Among them, you’ll find agents who don’t want the truth to emerge. They’ll try to sabotage your good efforts every which way they can.

DON’T LET THEM.


SOURCES:

[1] https://blog.nomorefakenews.com/2020/12/03/lockdowns-are-based-on-fraud-open-letter-to-people-who-want-freedom/

[2] https://www.youtube.com/watch?v=a_Vy6fgaBPE

[3] https://www.fda.gov/media/134922/download

[4] https://www.flhealthsource.gov/files/Laboratory-Reporting-CT-Values-12032020.pdf

 

 




Pathologist Petitions FDA to Halt Pfizer Emergency Use Authorization Until Vaccine Efficacy Confirmed

Pathologist Petitions FDA to Halt Pfizer Emergency Use Authorization Until Vaccine Efficacy Confirmed
The major reason for petitioning the FDA for a stay of action is that the Phase 2/3 clinical trial of the Pfizer vaccine used a presumptive RT-qPCR diagnostic test.

by Informed Consent Action Network
sourced from The Defender, Children’s Health Defense
December 7, 2020

 

Connecticut pathologist Dr. Sin Hang Lee and Informed Consent Action Network (ICAN) have petitioned the U.S. Food and Drug Administration (FDA) to require accurate counts of COVID-19 cases in the Pfizer/BioNTech COVID-19 mRNA vaccine trial.

“Until an accurate count of COVID-19 cases in the vaccinated and placebo groups has been determined for vaccine efficacy evaluation, we are asking the FDA to stay its decision regarding the emergency use authorization for this vaccine,” said Dr. Lee, director of Milford Molecular Diagnostics Laboratory.

The major reason for petitioning the FDA for a stay of action is that the Phase 2/3 clinical trial of the Pfizer vaccine used a presumptive RT-qPCR diagnostic test. This test is acknowledged by the medical science community to generate high rates of false-positive results among qualified trial participants from the placebo group with minor symptoms such as a sore throat or a new cough. This is especially evident when a de facto unblinding among the trial participants has taken place, according to the petition.

The Pfizer/BioNTech vaccine trial primarily uses an RT-qPCR test that employs cycle thresholds possibly up to 44.9 to identify COVID-19 “cases.” Samples deemed positive that require high levels of amplification (cycle thresholds greater than 30 to 35) are usually false positives, said Dr. Lee.

A recent review of a COVID-19 PCR test, which was signed by 22 international scientists, emphatically stated:

“To determine whether the amplified products are indeed SARS-CoV-2 genes, biomolecular validation of amplified PCR products is essential. For a diagnostic test, this validation is an absolute must. Validation of PCR products should be performed by either running the PCR product in a 1% agarose-EtBr gel together with a size indicator (DNA ruler or DNA ladder) so that the size of the product can be estimated. The size must correspond to the calculated size of the amplification product. But it is even better to sequence the amplification product. The latter will give 100% certainty about the identity of the amplification product. Without molecular validation one cannot be sure about the identity of the amplified PCR products…”

A recent petition to the European Medicines Agency to stay their COVID-19 vaccine trials used similar arguments regarding the inaccuracy of the PCR tests being used and the need for confirmatory sequencing.

On Dec. 1, Switzerland’s medical regulator, Swissmedic, said it lacks the necessary information to approve three different coronavirus vaccines ordered by the government, including the Pfizer vaccine.

In a recent interview about the pending review of the Pfizer COVID-19 vaccine, FDA Commissioner Stephen Hahn has promised, “we will make a determination regarding safety and efficacy based upon our very stringent criteria.”

As stated in the petition, if Pfizer is unable to perform the needed sequencing tests on the 180 RNA samples to confirm their stated vaccine efficacy rate of 95%, Dr. Lee has offered to re-test the residues of these samples in his laboratory.

Dr. Lee said his laboratory is located only one hour’s driving distance from Connecticut-based Pfizer Inc., and he will submit all the testing data to the FDA to support its vaccine evaluation based upon “very stringent criteria,” as promised by the FDA Commissioner.

Dr. Lee’s Sanger sequencing-based method for molecular diagnosis of SARS-CoV-2 was published in International Journal of Geriatrics and Rehabilitation.




New Details in COVID Testing Scandal

New Details in COVID Testing Scandal

by Del Bigtree with Jefferey Jaxen, The HighWire
December 7 2020

 



New details have emerged about the test used for #COVID19, highlighting serious inaccuracies in results and past comments by the tests’ creator doubting the accuracy of PCR testing.

German virologist Christian Drosten’s guidelines on detection of the novel coronavirus for the PCR tests was accepted after only 24 hours of surveillance before becoming the standard. His paper is now being contested and peer reviewed for the first time allowing for some shocking discoveries of error that would potentially render the PCR test completely useless.

#PCRTests #Casedemic #Covid19




UK Braces for Pfizer’s Experimental Shot

UK Braces for Pfizer’s Experimental Shot

by Jefferey Jaxen, The HighWire
December 7, 2020

 

Last week, the United Kingdom jumped in front of all other Western nations when it was the first to give emergency approval to Pfizer’s experimental Covid vaccine.

As Pfizer’s novel injectable product got the green light from Britain’s Medicines & Healthcare products Regulatory Agency (MHRA), The New York Times wrote:

“European regulators on Wednesday cast doubt on the rigor of Britain’s review and said that the authorization was limited to specific batches of the vaccine, a claim that Pfizer denied and British officials did not address.”

Echoing the doubt in part was Switzerland’s medical regulator Swissmedic publicly declared necessary information was lacking, and it would not sign off on three different coronavirus vaccines [Pfizer, Moderna and AstraZeneca’s] ordered by the Swiss government.

Swissinfo.ch noted: “The regulator said important data on safety, efficacy and quality are still missing. It has reached out to the manufacturers, who provided data from their studies.”

At a press briefing last Tuesday organized by the Federal Office of Public Health., Swissmedic’s Claus Bolte threw down the gauntlet: “We lack data on the effectiveness of the clinical trials and on the important subgroups that participated in these large studies,” Bolte, head of the authorization division, explained as Swissmedic demurred from endorsing the unproven jabs.

Nevertheless the UK marched forward with their strategy, echoed by most nations around the  world, to target frontline health workers and everyone who lives or works in long term care facilities, for the first round of experimental vaccines.

Swaths of the medical community are increasingly hesitant at being… steamrolled? Socially pressured? Coerced? Given an offer they can’t refuse?…into becoming Phase 4 Post-Marketing data points for Pfizer’s experimental vaccine – and for good reason!

Until recently, the bulk of scientific data known publicly about Pfizer’s shot came via the company’s carefully worded press releases. This inconvenient truth has dawned on the medical community who are first in line for the shot.

Doctors and nurses are not convinced about the vaccine data. To those ends, large health systems, medical societies and the federal government are launching an effort to persuade front-line health-care providers to take experimental shots.

A rushed propaganda arm is kicking into gear behind the scenes in an attempt to quell widespread vaccine hesitancy erupting within the medical community.  Unanswered questions, lack of transparency, questionable safety profiles, absent liability and the limited trial endpoints of the experimental vaccines deserve further public debate before premature assumptions of widespread uptake are made by health officials and national leaders.

In the US, vaccine-makers are given legal protection from any injuries or death caused by their injectable products. Outside America, this concept is foreign and scoffed at (as it should be!), by citizens of other countries. After the rushed approval of Pfizer’s shot, the UK population received a sobering lesson in Big Pharma’s modus operandi.

Mere days after the UK gave Pfizer’s Covid vaccine the green light, Pfizer’s Department of Health and Social Care confirmed the company had also been given indemnity protecting it from legal action as a result of any problems with the vaccine.

Simultaneously, in the true spirit of transparency, Pfizer’s UK management spoke to journalists at a press conference but refused to explain why the company needed an indemnity, according to The Independent: “We’re not actually disclosing any of the details around any of the aspects of that agreement and specifically around the liability clauses.”

Ministers have also changed the law in recent weeks to give new protections to companies such as Pfizer, giving them immunity from being sued by patients in the event of any complications, according to reports.

The UK government has published information regarding Pfizer’s COVID-19 mRNA Vaccine BNT162b2 for UK health professionals. Comprised of the latest, most up-to-date data and science, from the company itself, the information leaflet notes the following points:

“It is unknown whether COVID-19 mRNA Vaccine BNT162b2 has an impact on fertility.”

“Animal studies into potential toxicity to reproduction and development have not been completed.”

“The most frequent adverse reactions in participants 16 years of age and older were pain at the injection site (> 80%), fatigue (> 60%), headache (> 50%), myalgia (> 30%), chills (> 30%), arthralgia (> 20%) and pyrexia (> 10%) and were usually mild or moderate in intensity and resolved within a few days after vaccination.”

“In the absence of compatibility studies, this medicinal product must not be mixed with other medicinal products.” 

Major bombshell’s were delivered last week. The first one was from doctors Wolfgang Wodarg and Michael Yeadon, in the form of a legal petition to the European Medicines Agency. They have demanded a “stay,” or halt, to Phase III trials of Pfizer’s BNT162 in Germany, and in all other EU protocol countries until study design is amended.

The doctors deemed the current study designs for the Phase II/III trials of Pfizer/BioNTech to be inadequate for several reasons.

One such reason are that the clinical trials for new experimental Covid vaccines candidates, which use polymerase chain reaction (PCR) tests as the primary evidence of infection, are inadequate to accurately assess efficacy, say the doctors.

Along the lines of understanding safety, or a lack thereof, the doctors also raised the very real issue of Antibody Dependent Enhancement (ADE). This is a common problem with the family of coronaviruses and a major, well-documented reason why many previous vaccine trials for other coronaviruses failed.

The doctors write: “Major safety concerns were observed in animal models. If ADE occurs in an individual, their response to the virus can be worse than their response if they had never developed an antibody in the first place.”

Once thought to be a baseless theory, the admittedly untested effects on fertility from Pfizer’s shot has scientific standing to be questioned. The petition reads:

Syncytin-1…is derived from human endogenous retroviruses (HERV) and is responsible for the development of a placenta in mammals and humans and is therefore an essential prerequisite for a successful pregnancy, is also found in homologous form in the spike proteins of SARS viruses. There is no indication whether antibodies against spike proteins of SARS viruses would also act like anti-Syncytin-1 antibodies. However, if this were to be the case this would then also prevent the formation of a placenta which would result in vaccinated women essentially becoming infertile. To my knowledge, Pfizer/BioNTech has yet to release any samples of written materials provided to patients, so it is unclear what, if any, information regarding (potential) fertility-specific risks caused by antibodies is included.

Here’s EMA co-petitioner Dr. Wolfgang Wodarg speaking about his action in a recent interview with Del Bigtree on The HighWire:

https://thehighwire.com/videos/health-expert-stop-covid-vax-experiments/

Threaded throughout the paper was information discovered from the second major bombshell: The paper purporting to validate the primary RT-PCR test to detect SARS-CoV-2 used since January for the detection of coronavirus has been deemed “useless” by an external peer-review.

This is the same test used to determine if the new Covid vaccines are effective! Starting to see the house of cards yet? Listen to this guy:

Dr. Michael Yeadon, co-petitioner on the EMA legal document and one of the 22 medical professionals who has signed onto the external peer-review of the PCR test. This interview is with talkRADIO’s Julia Hartley-Brewer:



 




$218 MILLION Paid Out for Vaccine Injuries and Deaths in 2020 for FDA Approved Vaccines (NOT Fast-tracked)

$218 MILLION Paid Out for Vaccine Injuries and Deaths in 2020 for FDA Approved Vaccines (NOT Fast-tracked)

by Brian Shilhavy, Health Impact News
December 6, 2020

 

The federal government Advisory Commission on Childhood Vaccines (ACCV) under the U.S. Department of Health and Human Services met on December 3, 2020, and the Department of Justice reported that during a 3-month period from August 16th through November 15th this year, 166 cases of vaccine injuries were compensated through the National Vaccine Injury Compensation Program (NVICP).

You can read the full report here.

The NVICP was started as a result of a law passed in 1986 that gave pharmaceutical companies legal immunity from being sued due to injuries and deaths resulting from vaccines.

Today, anyone suffering from a vaccine injury or death must sue the U.S. Government and go up against their top attorneys.

In the fiscal year 2020 the NVICP has paid out $218 MILLION in damages due to vaccine injuries and deaths. (Source.)

Health Impact News is the only media source I am aware of that covers these quarterly meetings, and if we were to try and share articles like this one publishing these government reports, we would be accused of publishing “fake news.” (Previous reports are listed here.)

But as you can clearly see by clicking on these links, all of these reports were submitted during their quarterly meeting on December 3, 2020, and are stored on the Health Resources & Services Administration government website.

So clearly the various “fact checkers” and Big Tech social media companies define “real news” as only what appears on the Big Pharma and government-endorsed corporate media outlets. Anything outside of that is “fake news” to them if it disagrees with what they want you to know, and has absolutely nothing to do with the truth at all.

The $218 MILLION paid out for vaccine injuries and deaths this year was NOT paid by the pharmaceutical manufacturers. It is funded from taxes paid on each vaccine, and as of September 30, 2020, that fund had a balance of over $4 BILLION. (Source – p. 10)

The other thing to understand is that these funds are paid on vaccines that have gone through the FDA full approval process, not fast-tracked vaccines approved for emergency use. It typically takes 5 to 7 years to bring a new vaccine to market.

So none of these funds will be available to anyone who suffers injuries or dies due to the FDA fast-tracked for emergency use authorization (EUA) experimental COVID19 mRNA vaccine.

Injuries and deaths due to those vaccines fall under a different program, the CounterMeasures Injury Compensation Program (CICP).

There are several differences between the NVICP and CICP:

The CICP is designed to handle pandemic or other health emergency countermeasures as declared by the Secretary of HHS, and this will be the likely landing spot initially for any injuries or deaths alleged as a result of receiving a COVID-19 vaccine.

First, the CICP does not allow the petitioner to seek reimbursement of attorney fees nor medical expert costs.

In the NVICP, these costs are reimbursable even when the petitioner loses as long as the initial claim was shown to have a reasonable basis.

These costs can run on average of $35,000 to $75,000 and as high as $300,000.

I doubt if many petitioners can afford this cost out of their own pocket. So you are basically on your own: just you and the Secretary of HHS.

A second reason is that when you submit your petition, copies of your medical records need to be included. And that is all.

In the NVICP, generally your attorney will also submit research studies, expert reports to support your claim, but not so in the CICP.

A third reason is that if you are one of the very few who have been compensated in the CICP (8%), there is no award for pain & suffering, and no award for loss of future wages.

There is in the NVICP, up to $250,000 for pain & suffering.

Currently, nearly 74% of all claims are compensated in the NVICP, granted the vast majority are influenza vaccines administered to adults claiming shoulder injury or Guillain-Barre syndrome (GBS).

A forth reason is that there is no judicial appeal process; no higher court to appeal.

In the CICP, the appeal process is limited to appealing to the Secretary of HHS who determined the fate of your petition in the first place.

Renee Gentry, a Washington DC based attorney who practices in the NVICP, was quoted on my podcast Right on Point, with the following:

“In the CICP, you have the right to file a petition and lose.”

Think about that.

Read the full article here.

In short, your government is lying to you. They have been telling the public for years that all vaccines are “safe and effective,” and that the “science is settled.”

This lie is then proclaimed through the Pharma-funded corporate media, and any dissenting voices are vigorously censored.

And this has always been for vaccines that went through the full, lengthy FDA approval process.

Why would you start believing them now when they are fully admitting that the new COVID vaccines are being fast-tracked, and that the mRNA vaccines are an entirely new class of vaccine never before distributed to the public?

Comment on this article at VaccineImpact.com.




Do You Trust A Pharm Tech to Administer the Most Complex Vaccine In Human History?

Do You Trust A Pharm Tech to Administer the Most Complex Vaccine In Human History?

by Age of Autism
December 6, 2020

 

CVS is hiring THOUSANDS of pharmacy technicians and pharmacists to administer the Covid vaccine.

Pharmacy interns and techs who meet HHS requirements can administer childhood, COVID-19 vaccines

I am not belittling the career choice of pharma tech. But you should know that a person with a high school diploma or GED who makes $21,000 will be injecting you with this brand new vaccine. A Pharmacy Intern is a pharmacy school student. The vaccine needs to be stored, thawed, mixed, spoken to in a soft voice and told that it is the prettiest vaccine ever according to documentation. UK Pfizer Covid Doc – Read it

Salary for a Pharm Teach ranges from high $20Ks to low $30Ks. Source Zip recruiter

From the CVS hiring site:

Education: High School diploma or equivalent (preferred).

UK Pfizer Covid Doc – Read it

The rushed vaccine is gasoline. Add human error?




What’s Not Being Said About the Pfizer Coronavirus Vaccine. “Human Guinea Pigs”?

What’s Not Being Said About the Pfizer Coronavirus Vaccine. “Human Guinea Pigs”?

by F. William Engdahl, GlobalResearch
December 5, 2020

 

Bill Gates is actively financing and promoting new untested vaccines supposed to keep us at least somewhat safe from a ‘ghastly” death from the novel coronavirus and supposedly allow us to resume somewhat “normal” lives. The Pharma giant Pfizer has now announced what they claim were spectacular results in initial human tests. They use an experimental technology known as gene editing, specifically mRNA gene-editing, something never before used in vaccines. Before we rush to get jabbed in hopes of some immunity, we should know more about the radical experimental technology and its lack of precision.

The financial world went ballistic on November 9 when the pharma giant Pfizer and its German partner, BioNTech, announced in a company press release that it had developed a vaccine for Covid19 that was “90%” effective.

The controversial US head of NIAID, Tony Fauci (right) rushed to greet the news and the EU announced it had purchased 300 million doses of the costly new vaccine. If you believe financial markets, the pandemic is all but past history.

Suspicious events

However it seems Albert Bourla, the CEO of Pfizer, doesn’t share the confidence of his own claims. On the day his company issued its press release on the proposed vaccine trials, he sold 62% of his stock in Pfizer, making millions profit in the deal. He made the sell order in a special option in August so it would not appear as “insider selling”, however he also timed it just after the US elections and the mainstream media illegitimately declared Joe Biden President-elect. It seems from appearances that Bourla had a pretty clear conflict of interest in the timing of his press release on the same day.

Bourla lied and denied to the Press that his company had received any funds from the Trump Administration to develop the vaccine when it came out they contracted in summer to deliver 100 million doses to the US Government. Further adding to the suspect actions of Pfizer was the fact the company first informed the team of Joe biden rather than the relevant US government agencies.

But this is far from the only thing alarming about the much-hyped Pfizer announcement.

The German Partner

Pfizer, famous for its Viagra and other drugs, has partnered with a small Mainz, Germany company, BioNTech, which has developed the radical mRNA technique used to produce the new corona vaccine. BioNTech was only founded in 2008. BioNTech signed an agreement with the Bill & Melinda Gates Foundation in September, 2019, just before announcement in Wuhan China of the Novel Coronavirus and just before BioNTech made its stock market debut. The agreement involved cooperation on developing new mRNA techniques to treat cancer and HIV. Curiously that press release, “The Gates Foundation sees BioNTech potential to ‘dramatically reduce global HIV and tuberculosis’” 05. September 2019, has now been deleted.

BioNTech also has an agreement with one of the largest drug producers in China, Shanghai Fosun Pharmaceutical Co., Ltd (“Fosun Pharma”) to develop a version of its mRNA vaccine for novel coronavirus for the Chinese market. Ai-Min Hui, President of Global R&D of Fosun Pharma said in an August statement, “Dosing the first Chinese subject with BNT162b1 marks a milestone of the global co-development program in China. We are closely working with BioNTech and regulatory authorities to evaluate the safety and efficacy of BNT162b1 and other mRNA vaccine candidates…”

This means that the same German biotech company is behind the covid vaccines being rushed out in China as well as the USA and EU. The vaccine is being rushed through to eventual approval in an alarmingly short time.

Both US and EU authorities and presumably also Chinese, waived the standard animal tests using ferrets or mice and have gone straight to human “guinea pigs.” Human tests began in late July and early August. Three months is unheard of for testing a new vaccine. Several years is the norm. Because of the degree of global panic engendered by WHO over the coronavirus, caution is thrown to the wind. Vaccine makers all have legal indemnity, meaning they can’t be sued if people die or are maimed from the new vaccine. But the most alarming fact about the new Pfizer-BioNTech gene edited vaccine is that the gene edited mRNA for human vaccine application has never before been approved. Notably, two year peer reviewed tests with mice fed genetically modified corn sprayed with Monsanto glyphosate-rich Roundup first showed cancer tumors after nine months as well as liver and other organ damage. Earlier Monsanto company tests ended at three months and claimed no harm. A similar situation exists with the gene edited mRNA vaccines that are being rushed out after less than 90 days human tests.

“Explicitly experimental”

Dr. Michael Yeadon replied in a recent public social media comment to a colleague in the UK; “All vaccines against the SARS-COV-2 virus are by definition novel. No candidate vaccine has been… in development for more than a few months.” Yeadon then went on to declare,

“If any such vaccine is approved for use under any circumstances that are not EXPLICITLY experimental, I believe that recipients are being misled to a criminal extent. This is because there are precisely zero human volunteers for…whom there could possibly be more than a few months past-dose safety information.”

Yeadon is well qualified to make the critique. As he notes in the comment, “I have a degree in Biochemistry & Toxicology & a research based PhD in pharmacology. I have spent 32 years working in pharmaceutical R&D, mostly in new medicines for disorders of lung & skin. I was a VP at Pfizer & CEO…. of a biotech I founded (Ziarco – acquired by Novartis). I’m knowledgeable about new medicine R&D.” He was formerly with Pfizer at a very senior level.

Human guinea pigs?

The Pfizer-BioNTech vaccine is experimental and far from guaranteed safe, despite the fact that Pfizer, the EU and the notorious Dr Tony Fauci seem ready to roll it out even before year end to hundreds of millions of humans.

The experimental technology is based on a rather new gene manipulation known as gene editing. In a major article in the 2018 New York Council on Foreign Relations magazine, Foreign Affairs, Bill Gates effusively promoted the novel gene editing CRISPR technology as being able to “transform global development.” He noted that his Gates Foundation had been financing gene editing developments for vaccines and other applications for a decade.

But is the technology for breaking and splicing of human genes so absolutely safe that it is worth risking on a novel experimental vaccine never before used on humans? Contrary to what Bill Gates claims, the scientific answer is no, it is not proven so safe.

In a peer reviewed article in the October, 2020 journal Trends in Genetics, the authors conclude that “the range of possible molecular events resulting from genome editing has been underestimated and the technology remains unpredictable on, and away from, the target locus.”

Dr. Romeo Quijano, retired professor of Pharmacology and Toxicology at the College of Medicine, University of the Philippines Manila, noted some of the dangers of the experimental gene editing when applied to human vaccines. Quijano warns of,

“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. 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.”

He cites the case of another Gates mRNA vaccine candidate, Moderna, where “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…”

He notes,

“Exogenous mRNA is inherently immune-stimulatory, 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.” Quijano adds, “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… and may promote blood coagulation and pathological thrombus formation.”

Quijano writes in the extensively documented article,

“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…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.”

Bill Gates, the mRNA vaccine makers including Pfizer/BioNTech and Moderna, and their close allies such as Dr. Tony Fauci of the NIAID are clearly playing fast and loose with human lives in their rush to get these experimental vaccines into our bodies. Notably, the same Dr. Fauci and his NIAID owns the patent on a vaccine for dengue fever known as Dengvaxia, marketed by Sanofi-Pasteur and promoted as an “essential” vaccine by Tedros’ WHO since 2016. Robert F. Kennedy Jr. (right) noted that Fauci and NIAID “knew from the clinical trials that there was a problem with paradoxical immune response,” but they gave it to several hundred thousand Filipino kids anyway. It was estimated that as many as 600 vaccinated children died before the government stopped the vaccinations.

Clearly the well-established Precautionary Principle–if in serious doubt, don’t– is being ignored by Fauci, Pfizer/BioNTech and others in rushing to approve the new mRNA vaccine for coronavirus. Messenger RNA technology has yet to produce an approved medicine, let alone a vaccine.




Bill Gates on How the New Vaccine Is Designed to Change Our DNA Forever

Bill Gates on How the New Vaccine Is Designed to Change Our DNA Forever

 

 




Vaccine Risk Event Goes Global

Vaccine Risk Event Goes Global

by Del Bigtree, The HighWire
December 4, 2020



This past week, vaccine safety advocates put up informative banners across major highways throughout all 50 states and in 3 countries.

Del chats with organizers Joshua Coleman and Olivia Mikos from V is for Vaccine who used the biggest traffic day of the year to their advantage to draw attention to #Covid19 vaccine safety.

#V4Vaccine #V4VGlobalDemo #VaccineTrials #VaccineSafety

V is for Vaccine: https://www.visforvaccine.com/




What We Know So Far About U.S. Government’s Plan to Track COVID Vaccine Recipients

What We Know So Far About U.S. Government’s Plan to Track COVID Vaccine Recipients

To track COVID vaccine recipients, Operation Warp Speed has resurrected a program devised after the September 11 attacks that was quickly defunded following public backlash over privacy concerns.

by Dr. Joseph Mercola
sourced from The Defender, Children’s Health Defense
December 3, 2020

 

Story at-a-glance:

  • Operation Warp Speed (OWS), a joint operation between U.S. Health and Human Services and the Department of Defense, continues to be shrouded in secrecy.
  • OWS is a public-private partnership tasked with producing therapeutics and a fast-tracked COVID-19 vaccine — 300 million doses’ worth that are intended to be made available starting in January 2021.
  • OWS has plans to engage an “active pharmacovigilance surveillance system” to track Americans for 24 months following vaccination.
  • One of OWS’ four key tenets is “traceability,” which includes confirming which of the approved vaccines were administered regardless of location (public or private), reminding recipients to return for a second dose and ensuring that the correct second dose is administered.
  • Google and Oracle, multinational computer technology corporations headquartered in California, in the heart of Silicon Valley, have been contracted to “collect and track vaccine data” as part of OWS’ surveillance systems.
  • OWS, rather than being directed by public health officials, is heavily dominated by military, technology companies and U.S. intelligence agencies, likening it to a successor for Total Information Awareness (TIA), a program that sprang up after the September 11 attacks but was quickly defunded following public backlash over privacy concerns.

Operation Warp Speed, a joint operation between U.S. Health and Human Services (HHS) and the Department of Defense (DOD), continues to be shrouded in secrecy, but little by little information is emerging that long-term monitoring of the U.S. public is part of the plan.

At face value, OWS is a public-private partnership tasked with producing therapeutics and a fast-tracked COVID-19 vaccine — 300 million doses’ worth that are intended to be made available starting in January 2021.

But it appears the involvement doesn’t end there. Rather than just ensuring a vaccine is produced and made available for those who want it, Moncef Slaoui, the chief scientific adviser for Operation Warp Speed, dubbed the coronavirus vaccine czar, said in an interview with The Wall Street Journal that the rollout will include “incredibly precise … tracking systems.”

Their purpose? “To ensure that patients each get two doses of the same vaccine and to monitor them for adverse health effects.” In an interview with The New York Times, Slaoui described it as a “very active pharmacovigilance surveillance system.”

What will the vaccine monitoring system entail?

This is the number one question, and one that hasn’t been answered, at least not officially. “While Slaoui himself was short on specifics regarding this ‘pharmacovigilance surveillance system,’” news outlet Humans Are Free reported, “the few official documents from OWS that have been publicly released offer some details about what this system may look like and how long it is expected to ‘track’ the vital signs and whereabouts of Americans who receive a Warp Speed vaccine.”

One of the documents, “From the Factory to the Frontlines: The Operation Warp Speed Strategy for Distributing a COVID-19 Vaccine,” was released by HHS. It also mentions the use of pharmacovigilance surveillance along with Phase 4 (post-licensure) clinical trials in order to assess the vaccines’ long-term safety, since “some technologies have limited previous data on safety in humans.”

The report, which lays out a strategy for distributing a COVID-19 vaccine, from allocation and distribution to administration and more, continues:

“The key objective of pharmacovigilance is to determine each vaccine’s performance in real-life scenarios, to study efficacy, and to discover any infrequent and rare side effects not identified in clinical trials. OWS will also use pharmacovigilance analytics, which serves as one of the instruments for the continuous monitoring of pharmacovigilance data.

“Robust analytical tools will be used to leverage large amounts of data and the benefits of using such data across the value chain, including regulatory obligations. Pharmacovigilance provides timely information about the safety of each vaccine to patients, healthcare professionals, and the public, contributing to the protection of patients and the promotion of public health.”

Similar language was reiterated in an October 2020 perspective article published in The New England Journal of Medicine (NEJM), written by Slaoui and Dr. Matthew Hepburn.

Hepburn is a former program manager for the U.S. Defense Advanced Research Projects Agency (DARPA), where he oversaw the development of Profusa an implantable biosensor that allows a person’s physiology to be examined at a distance via smartphone connectivity. Profusa is also backed by Google, the largest data mining company in the world.

In NEJM, the duo writes, “Because some technologies have limited previous data on safety in humans, the long-term safety of these vaccines will be carefully assessed using pharmacovigilance surveillance strategies.”

‘Traceability’ a key tenet of operation warp speed

Humans Are Free also references an OWS infographic, which details the COVID-19 vaccine distribution and administration process. One of the four key tenets is “traceability,” which includes confirming which of the approved vaccines were administered regardless of location (public or private), reminding recipients to return for a second dose and ensuring that the correct second dose is administered.

That word — pharmacovigilance — is used again, this time as a heading inferring that the U.S. Food and Drug Administration and the U.S. Centers for Disease Control and Prevention will be involved in “24-month post trial monitoring for adverse effects/additional safety feature.” Pharmacovigilance, also known as drug safety, generally refers to the collection, analysis, monitoring and prevention of adverse effects from medications and other therapies.

Passive reporting systems for adverse events, like the Vaccines Adverse Event Reporting System, already exist and are managed by the FDA and CDC.

However, a report released by Johns Hopkins Bloomberg School of Public Health, Center for Health Security suggests that passive systems that rely on people to send in their experiences should be made into an “active safety surveillance system directed by the CDC that monitors all vaccine recipients — perhaps by short message service or other electronic mechanisms — with criteria based on the World Health Organization Global Vaccine Safety Initiative.”

What’s more, according to Humans Are Free, “Despite the claims in these documents that the ‘pharmacovigilance surveillance system’ would intimately involve the FDA, top FDA officials stated in September that they were barred from attending OWS meetings and told reporters they could not explain the operation’s organization or when or with what frequency its leadership meets.” STAT News further reported:

“The Food and Drug Administration, which is playing a critical role in the response to the pandemic, has virtually no visibility into OWS — but that’s by design … The FDA has set up a firewall between the vast majority of staff and the initiative to separate any regulatory decisions from policy or budgetary decisions.

“FDA officials are still allowed to interact with companies developing products for OWS, but they’re barred from sitting in on discussions regarding other focuses of OWS, like procurement, investment or distribution.”

Johns Hopkins Bloomberg School of Public Health, Center for Health Security, by the way, has ties to Event 201, a pandemic preparedness simulation for a “novel coronavirus” that took place in October 2019, along with Dark Winter, another simulation that took place in June 2001, which predicted major aspects of the subsequent 2001 anthrax attacks.

Hepburn also reportedly “ruffled feathers” during a June 2020 presentation to the CDC’s Advisory Committee on Immunization Practices because he offered no data-rich slides, which are typically part of such presentations, and, STAT News reported, “Several members asked Hepburn pointed questions he pointedly did not answer.”

Google and Oracle contracted to collect vaccine data

Google and Oracle, multinational computer technology corporations headquartered in California, in the heart of Silicon Valley, have been contracted to “collect and track vaccine data” as part of OWS’ surveillance systems, a partnership Slaoui reportedly revealed in his Wall Street Journal interviewAccording to Humans Are Free:

“If the Warp Speed contracts that have been awarded to Google and Oracle are anything like the Warp Speed contracts awarded to most of its participating vaccine companies, then those contracts grant those companies diminished federal oversight and exemptions from federal laws and regulations designed to protect taxpayer interests in the pursuit of the work stipulated in the contract.

“It also makes them essentially immune to Freedom of Information Act requests. Yet, in contrast to the unacknowledged Google and Oracle contracts, vaccine companies have publicly disclosed that they received OWS contracts, just not the terms or details of those contracts. This suggests that the Google and Oracle contracts are even more secretive.”

In an interview with investigative journalist Whitney Webb, it’s also revealed that Slaoui, a long-time head of GlaxoSmithKline’s vaccine division, is a leading proponent of bioelectronic medicine, which is the use of injectable or implantable technology for the purpose of treating nerve conditions.

The MIT Technology review has referred to it as hacking the nervous system. But it also allows monitoring of the physiology of the human body from the inside.

Slaoui is also invested in a company called Galvani Bioelectronics, which was cofounded by a Google subsidiary. “So, you have Google being contracted to monitor this pharmacovigilance surveillance system that aims to monitor the physiology and the human body for two years,” Webb says.

“And then you have the ties to the Profusa project,” she adds, “which oddly enough is supposed to work inside the human body for 24 months — the exact window they’ve said will be used to monitor people after the first [vaccine] dose.”

The conflict of interest is massive, in part because Google owns YouTube, which has been banning our videos, a majority of which are interviews with health experts sharing their medical or scientific expertise and viewpoints on COVID-19, since June 2020. As noted by Humans Are Free:

“With Google now formally part of OWS, it seems likely that any concerns about OWS’s extreme secrecy and the conflicts of interest of many of its members (particularly Moncef Slaoui and Matt Hepburn) as well as any concerns about Warp Speed vaccine safety, allocation and/or distribution may be labeled ‘COVID-19 vaccine misinformation’ and removed from YouTube.”

Is total surveillance set to become the new normal?

OWS, rather than being directed by public health officials, is heavily dominated by military, technology companies and U.S. intelligence agencies, likening it to a successor for TIA, a program managed by DARPA that sprang up after the September 11 attacks.

At the time, TIA was seeking to collect Americans’ medical records, fingerprints and other biometric data, along with DNA and records relating to personal finances, travel and media consumption. According to Webb:

“We now know, for example, that the NSA and the Department of Homeland Security are directly involved in Operation Warp Speed, But there are some indications as to what they could be involved with.

“And the fact that Silicon Valley companies that have been known to collaborate with intelligence [agencies] for the purpose of spying on innocent Americans — Google and Oracle, for example — are going to be involved in this surveillance system … for everyone that gets the vaccine.

“It’s certainly alarming, and it seems to point to the fulfillment of an agenda that was attempted to be pushed through or foisted on the American public after September 11, called Total Information Awareness, which was managed, originally, by DARPA.

“It was about using medical data and non-medical data — essentially all data about you — to prevent terror attacks before they could happen, and also to prevent bioterror attacks and even prevent naturally occurring disease outbreaks.

“A lot of the same initiatives proposed under that original program after September 11 have essentially been resurrected, with updated technology, under the guise of combating COVID-19.”

A key difference is that TIA was quickly defunded by Congress after significant public backlash, including concerns that TIA would undermine personal privacy. In the case of OWS, there’s little negative press and media outlets are overwhelmingly supportive of the operation as a way to resolve the COVID-19 crisis.

But what if it’s not actually about COVID-19 at all, but represents something bigger, something that’s been in the works for decades? As Humans Are Free puts it:

“The total-surveillance agenda that began with TIA and that has been resurrected through Warp Speed predated COVID-19 by decades.

“Its architects and proponents have worked to justify these extreme and invasive surveillance programs by marketing this agenda as the ‘solution’ to whatever Americans are most afraid of at any given time. It has very little to do with ‘public health’ and everything to do with total control.”

Published with permission from Mercola.




The Ruling Class Claims They Are Getting the COVID-19 Vaccine

The Ruling Class Claims They Are Getting the COVID-19 Vaccine

by Mac Slavo, SHTFplan.com
December 3, 2020

 

Bill Clinton, George W. Bush, and Barack Obama all say they will be getting the new Coronavirus vaccine. As if we didn’t trust the ruling class already, this should seal the deal. This is an obvious bit of propaganda.

The three former presidents from both sides of the aisle (political parasites and members of the ruling class) have all pledged to take a COVID-19 vaccine on camera when it’s available to them, hoping to assuage fears at a time when recent polls have shown that just under half of Americans said they would not take a vaccine, according to a report by Today. 

As Brian with High Impact TV says, “anytime a world leader takes a V-A-double-X on TV, it might behoove the general public to take a closer look.”



We know these three former presidents have all lied to us and deceived us, so the very idea of them taking the vaccine on video is laughable. Even if they do get a shot, does anyone honestly believe it’s anything more than a simple saline solution?  Wake up, folks. It’s 2020 and people are still falling for this.

Obama said on “The Joe Madison Show” on SiriusXM Wednesday that he was committed to taking a vaccine. “I promise you that when it’s then made for people who are less at risk, I will be taking it, and I may end up taking it on TV or having it filmed just so that people know that I trust this science, and what I don’t trust is getting COVID,” he said.

A statement by Bush aide Freddy Ford provided to NBC News and first reported by CNN indicated that the 43rd president (who lied extensively about weapons of mass destruction and 9/11 to send the troops into endless wars) would also be publicly taking the vaccine when it becomes available. “A few weeks ago President Bush asked me to let Dr. Fauci and Dr. Birx know that, when the time is right, he wants to do what he can to help encourage his fellow citizens to get vaccinated,” Ford said. “First, the vaccines need to be deemed safe and administered to the priority populations. Then, President Bush will get in line for his, and will gladly do so on camera.”

Not convinced yet? Well, let’s add in Bill Clinton. He’s been an honest and upstanding ruler, right? (That’s sarcasm.) Clinton’s staff indicated he would take the vaccine and potentially be filmed doing it, NBC News White House correspondent Kristen Welker reported on TODAY Thursday.

So that’s it! Roll up your sleeve and submit, slaves. The presidents are going to.  And there’s no way they’d ever lie and fake these videos of them getting the vaccine. Of course, they’ll be getting the same shot they want us to take… (sarcasm again)




Qantas Airlines: No Jab No Flight

Qantas Airlines: No Jab No Flight

by Del Bigtree with Jefferey Jaxen, The HighWire
December 4, 2020

 



The CEO of Australian airline Qantas triggered a frenzy by being the first major airline to announce their intention to require #Covid19 vaccines for their passengers. The HighWire reports.




Operation VECTOR Exposed — This Is Why the Coming Vaccine Rollout Must Be Rejected!

MUST SEE: Operation VECTOR Exposed — THIS Is Why The Coming Vaccine Rollout MUST BE REJECTED!!!

by Dan Dicks, Press for Truth
December 3, 2020

 

The Canadian Armed Forces have engaged operation VECTOR, its vaccine rollout plan to immunize the entire population of Canada.

The plan is being rushed through under the guise that COVID-19(84) is the biggest threat to humanity and therefore the military (who have recently been caught engaging in propaganda campaigns to scare the Canadian people) is now tasked with ensuring a nationwide rollout as early as Spring of 2021.

In this video Dan Dicks of Press For Truth exposes operation vector as a plan that must be avoided at all costs!

DO NOT get the shot because the shot IS the pandemic!



WATCH ON  BITCHUTE   FLOTE   LBRY   MINDS




Survivors of Lethal Drug & Shock Deep Sleep Therapy Vindicated After 30 Years

Survivors of Lethal Drug & Shock Deep Sleep Therapy Vindicated After 30 Years

An Australian judge’s condemnation of a dangerous psychiatric treatment linked to 48 deaths and once used in U.S. mind-control experiments, ignites new calls for a global ban on electroshock treatment.

by CCHR International
December 1, 2020

 

A recent finding by an Australian federal judge has vindicated hundreds of patients subjected to potentially lethal Deep Sleep Treatment (DST) involving heavy psychotropic drugs and electroshock. Jan Eastgate, the international president of CCHR, said CCHR helped get the practice banned in New South Wales in 1983 following 48 deaths. The group also exposed its use in U.S. Central Intelligence Agency (CIA)-funded brutal experiments during the 50s and 60s, where patients were electroshocked while in a drug-induced coma.[1] But a judgement on November 25, 2020 has reignited calls for electroshock treatment (ECT) used in DST to also be banned.

The Australian findings were in relation to two former DST doctors, Dr. John Gill and deregistered psychiatrist, John Herron, who questioned the publication of a 2016 book, the author of which had re-hashed the findings of a NSW Royal Commission into DST in 1988-1990, and other reports, including coroner inquests. CCHR and a nurse, Rosa Nicholson, had played a pivotal role in obtaining the re-opening of coroner inquests that linked DST to the deaths, and other actions leading to the $15 million government inquiry that condemned DST. Two DST doctors waited nearly 30 years to challenge the Commission findings that relied upon testimony from patients, CCHR, nurses, and international experts that condemned DST. The experts also were critical of the way in which ECT was practiced at the now-closed for-profit Chelmsford psychiatric hospital. (Read article on the case.)

In a multi-million-dollar court challenge, this year’s findings were the opposite of what the doctors had anticipated.[2] Judge Jayne Jagot of the Australian Federal Court NSW Registry reinforced the Royal Commission findings, stating the Commission’s report “exposed atrocities and horrors at Chelmsford and the applicants’ roles in perpetuating those atrocities and horrors on patients who, on any reasonable view, were the victims” of “gross negligence, unethical conduct and medical malpractice.”

Further, “In my view, the very nature of DST was dehumanizing and traumatizing. Patients and their families were not informed about what was proposed. Patients were rendered effectively comatose for no good reason, for lengthy periods, making them defenseless, helpless, and incontinent. While sedated they were subjected to ECT without anesthetic, oxygen or muscle relaxants.”

The case reflects problems that still exist with electroshock today, including in the U.S. As used in DST, Judge Jagot said: “Many patients were not told they would be given ECT, and if they had known, would never had allowed it.” Eastgate, whose CCHR headquarters are in Los Angeles, said: “In the U.S. today, statistics on the number of patients forced to undergo ECT without consent or based on misleading, if not fraudulent, information are not maintained. Consumer fraud is notorious, because often patients are not informed ECT causes brain damage.”

Judge Jagot also stated: “ECT was open to abuse and was routinely abused” at Chelmsford hospital. “This reinforces my conclusion that it is likely that no patient gave informed consent to DST because no patient would have knowingly consented to a procedure with such a serious risk of harm and death had they been informed (as they should have been) about available alternatives and that DST was an experimental and unproven procedure.”

Eastgate and the former Chelmsford Hospital whistle-blower nurse, the late Rosa Nicholson, worked together for many years exposing DST and ECT in Australia. Judge Jagot’s judgement reinforced the vindication Nicholson obtained in the Royal Commission. The nurse had photocopied records as evidence against DST, which CCHR turned over to the NSW Attorney General to act and which helped CCHR to get four coroner’s inquests re-opened.[3] Eastgate and Nicholson met following a DST psychiatrist, Dr. Harry Bailey, was publicly exposed for his sexual affair with a patient, Sharon Hamilton, that he’d electroshocked and her subsequent suicide. The psychiatrist, himself, was put under DST following Hamilton’s death and years later, in 1985, he, too, committed suicide.

When the DST case arose again this year after so many years, Eastgate wrote a tribute to the nurse to reinforce the facts about her work.

In 1980, Eastgate provided copies of Rosa’s photocopied records to 60 Minutes—described by them as a “sizable dossier on Chelmsford Hospital.” 60 Minutes’ award-winning expose called “The Chelmsford Scream,” also showed how “Politicians had been warned that things were dangerously out of control…The psychiatric profession closed ranks around their colleague [Bailey].” It had been known for years that something was gravely amiss at Chelmsford but 60 Minutes could not find a psychiatrist to speak out individually about it on camera. In fact, CCHR provided its co-founder, the late Dr. Thomas Szasz, then a professor of psychiatry based in New York, to comment.

Anthony McClellan, a director of the 60 Minutes programs on DST said words to the effect that “The 60 Minutes program would never have been aired if not for the documents provided by Ms Eastgate.” And, in turn, Nicholson, Eastgate said.

As Judge Jagot quoted, “Rosa Nicholson became the central figure in exposing the truth about the dozens of deaths caused by medical malpractice inside Chelmsford Hospital.” Further, her contribution “to the exposure of the iniquitous goings-on at Chelmsford was a worthwhile endeavour that has increased, not reduced, the total sum of human knowledge.”

In a united effort, patient survivors of DST, especially the late former actor, Barry Hart, their families, nurses, several journalists, legislators and CCHR, were instrumental in causing a legacy of patient rights, but which CCHR says are currently being undermined in Australia that has seen a nearly 50% increase in the use of ECT since 2010.

In the U.S., over 100,000 Americans every year are subjected to ECT, some aged 0-5, according to State information. The over $3 billion a year industry prompted CCHR’s latest documentary, Therapy or Torture? The Truth About Electroshock, which includes the story of DST.

The delivery of DST in NSW is a criminal offense under the NSW Mental Health Act, while in Western Australia, ECT is banned and carries a jail sentence and/or financial fine if administered to minors—all thanks to CCHR. In the U.S., CCHR and ECT survivors were also instrumental in obtaining a ban on ECT use on minors in four states. CCHR wants to see such a ban extend to all age groups globally.

An online petition also supports a ban on ECT.

Judge Jagot said she had “formed strong impressions of Dr Gill and Mr Herron… They were unable to accept criticisms of their treatment of their patients and patients generally in Chelmsford who were administered DST and ECT. They appeared powerfully motivated by a need to see themselves vindicated from the serious adverse findings made by the Royal Commission against them. Their entire approach to their conduct was self-justificatory and self-exculpatory [free of guilt].”

Eastgate added the recent decision also vindicated CCHR and the Church of Scientology that established it in 1969 to investigate and expose psychiatric violations of human rights. “The doctors tried to undermine the years of work it took to get inquests reopened, media coverage to raise awareness about the DST risks, the medical licensing board complaints Barry Hart and I filed against Herron and Bailey, the support given the Chelmsford Victims Action Group, and much more that culminated in the Royal Commission. These are documented events.”

As one article on the Chelmsford scandal summarized, “Its outcome was rightly not just condemnation of Bailey—but rather, an investigation into how mental health services should be regulated so as to prevent such individuals from so perniciously undermining the practitioner’s Hippocratic promise to ‘do no harm.’”[4]

CCHR International also encourages patients damaged by ECT or their families to report this to the group using its online abuse report form.

References:

[1] “1950s–1960s: Dr. Ewen Cameron Destroyed Minds at Allan Memorial Hospital in Montreal,” AARP, 18 Jan. 2015, https://ahrp.org/1950s-1960s-dr-ewen-cameron-destroyed-minds-at-allan-memorial-hospital-in-montreal/; “Deep Sleep Treatment Death Nightmare Awakes 30 Years Later to Condemn Current Psychiatric Practices,” TruthAboutECT.org, updated 27 Nov. 2020, https://truthaboutect.org/deep-sleep-treatment-death-nightmare-awakes-30-years-later/

[2] “‘Deep sleep therapy’ doctors lose multi-million-dollar fight to clear their names: Dr John Gill, a former GP and deregistered psychiatrist John Herron used defamation laws to try and ‘rewrite history,’” Australian Doctor, 26 Nov. 2020.

[3] John Adams inquest (26 Jan. 1978 and Jan. 1980); Sharon Hamilton (March/April 1979); Miriam Podio (1982); Audrey Francis (1986)

[4] https://chelmsfordblog.wordpress.com/




Will Face Masks Cause Facial Deformities in Children?

Will Face Masks Cause Facial Deformities in Children?

by John C. A. Manley, MuchAdoAboutCorona.ca
December 3, 2020

 

“When wearing a mask, most of us breathe with our upper chest muscles and with our mouth open,” states Children’s Minnesota on their website. While the hospital admits this can cause “increased stress and anxiety” there are other more long-lasting concerns.

According to a paper, in the peer-reviewed journal General Dentistry, “children’s whose mouth breathing is untreated” may develop the following deformities:

  • long, narrow faces
  • narrow mouths
  • high palatal vaults
  • misalignment between the teeth of the two dental arches
  • gummy smiles

As well as “many other unattractive facial features.”

Yet, how many children are being taught how to breathe while wearing a mask? Instead, many (if not most) are sucking in air through their mouth, as an instinctual reaction to the rise in carbon dioxide. This lowers the position of their tongue, which is key factor in normal facial development.

As the author of the paper, Dr. Yosh Jefferson, DMD, states: “If mouth breathing is treated early, its negative effect on facial and dental development and the medical and social problems associated with it can be reduced or averted.”

Instead, face masks may very well exacerbate the problem leading to a generation of deformed children. Because, it’s not just the mouth breathing. How will a growing face and two developing ears respond to a muzzle stretched around it for hours each day?

And, for what? There is no proof masks are effective at stopping infection. And, even if they were, children are practically immune from COVID-19 (a deadly disease that oddly focuses on old people who were on the verge of dying already).

But don’t worry, kids, if you grow up with an odd looking face all you have to do is… keep wearing your mask. No one will notice.

Facial deformities: Yet another reason to stop the masking madness.


 

John C. A. Manley has spent over a decade ghostwriting for medical doctors, as well as naturopaths, chiropractors and Ayurvedic physicians. He publishes the COVID-19(84) Red Pill Posts – an email-based newsletter dedicated to preventing the governments of the world from using an exaggerated pandemic as an excuse to violate our freedom, health, privacy, livelihood and humanity.  You can visit his website at: MuchAdoAboutCorona.ca




EPA Forced to Study Glyphosate, Finds Pesticide Could Injure or Kill 93% of Endangered Species

EPA Forced to Study Glyphosate, Finds Pesticide Could Injure or Kill 93% of Endangered Species

The long-anticipated draft biological evaluation released by the EPA found that 1,676 endangered species are likely to be harmed by glyphosate, the active ingredient in Monsanto’s Roundup, the world’s most-used pesticide.

by Center for Biological Diversity
sourced from The Defender, Children’s Health Defense

 

The U.S. Environmental Protection Agency (EPA) released a draft biological evaluation last week finding that glyphosate is likely to injure or kill 93% of the plants and animals protected under the Endangered Species Act.

The long-anticipated draft biological evaluation released by the agency’s pesticide office found that 1,676 endangered species are likely to be harmed by glyphosate, the active ingredient in Roundup and the world’s most-used pesticide.

The draft biological opinion also found that glyphosate adversely modifies critical habitat for 759 endangered species, or 96% of all species for which critical habitat has been designated.

“The hideous impacts of glyphosate on the nation’s most endangered species are impossible to ignore now,” said Lori Ann Burd, environmental health director at the Center for Biological Diversity. “Glyphosate use is so widespread that even the EPA’s notoriously industry-friendly pesticide office had to conclude that there are hardly any endangered species that can manage to evade its toxic impacts.

Hundreds of millions of pounds of glyphosate are used each year in the U.S., mostly in agriculture but also on lawns, gardens, landscaping, roadsides, schoolyards, national forests, rangelands, power lines and more.

According to the EPA, 280 million pounds of glyphosate are used just in agriculture, and glyphosate is sprayed on 298 million acres of crop land each year. 84% of glyphosate pounds applied in agriculture are applied to soy, corn and cotton, commodity crops that are genetically engineered to tolerate being drenched with quantities of glyphosate that would normally kill a plant.

Glyphosate is also widely used in fruit and vegetable production.

“As we prepare to feast on our favorite Thanksgiving dishes, the ugly truth of how harmful industrial-scale agriculture has become in the U.S. has never been so apparent,” said Burd. “If we want to stop the extinction of amazing creatures like monarch butterflies, we need the EPA to take action to stop the out-of-control spraying of deadly poisons.”

The EPA has, for decades, steadfastly refused to comply with its obligation under the Endangered Species Act to assess the harms of pesticides to protected plants and animals. But it was finally forced to do this evaluation under the terms of a 2016 legal agreement with the Center for Biological Diversity.

Emails obtained in litigation brought against Monsanto/Bayer by cancer victims and their families have uncovered a disturbingly cozy relationship between the agency and the company on matters involving the glyphosate risk assessment.

In one example, when the U.S. Department of Health and Human Services announced it would be reviewing glyphosate’s safety, an EPA official assured Monsanto he would work to thwart the review, saying, “If I can kill this, I should get a medal.” The Health and Human Services review was delayed for three years.

Monsanto/Bayer has also enjoyed broad support from the Trump White House. A domestic policy advisor in the Trump administration stated, “We have Monsanto’s back on pesticides regulation.”

Earlier this year, relying on confidential industry research, the EPA reapproved glyphosate. The EPA’s assessment contradicts a 2015 World Health Organization analysis of published research that determined glyphosate is a probable carcinogen.

President-elect Joe Biden has already tapped Michael McCabe, a former consultant to chemical giant DuPont, to join his Environmental Protection Agency transition board, drawing broad outrage, including from Erin Brockovich.




Warp Speed Ahead: COVID-19 Vaccines Pave the Way for a New Frontier in Surveillance

Warp Speed Ahead: COVID-19 Vaccines Pave the Way for a New Frontier in Surveillance

by John W. Whitehead, The Rutherford Institute
December 1, 2020

 

Man’s conquest of Nature, if the dreams of some scientific planners are realized, means the rule of a few hundreds of men over billions upon billions of men.” —C. S. Lewis, The Abolition of Man

Like it or not, the COVID-19 pandemic with its veiled threat of forced vaccinations, contact tracing, and genetically encoded vaccines is propelling humanity at warp speed into a whole new frontier—a surveillance matrix—the likes of which we’ve only previously encountered in science fiction.

Those who eye these developments with lingering mistrust have good reason to be leery: the government has long had a tendency to unleash untold horrors upon the world in the name of global conquest, the acquisition of greater wealth, scientific experimentation, and technological advances, all packaged in the guise of the greater good.

Indeed, “we the people” have been treated like lab rats by government agencies for decades now: caged, branded, experimented upon without our knowledge or consent, and then conveniently discarded and left to suffer from the after-effects.

You don’t have to dig very deep or go very back in the nation’s history to uncover numerous cases in which the government deliberately conducted secret experiments on an unsuspecting populacemaking healthy people sick by spraying them with chemicals, injecting them with infectious diseases and exposing them to airborne toxins.

Now this same government—which has taken every bit of technology sold to us as being in our best interests (GPS devices, surveillance, nonlethal weapons, etc.) and used it against us, to track, control and trap us—wants us to fall in line as it prepares to roll out COVID-19 vaccines that owe a great debt to the Pentagon’s Defense Advanced Research Projects Agency for its past work on how to weaponize and defend against infectious diseases.

The Trump Administration by way of the National Institute of Health awarded $22.8 million to seven corporations to develop artificial intelligence (AI), machine learning, etc., with smart phone apps, wearable devices and software “that can identify and trace contacts of infected individuals, keep track of verified COVID-19 test results, and monitor the health status of infected and potentially infected individuals.”

This is all part of Operation Warp Speed, which President Trump has likened to the Manhattan Project, a covert government effort spearheaded by the military to engineer and build the world’s first atomic bomb.

There is every reason to tread cautiously.

There is a sinister world beyond that which we perceive, one in which power players jockey for control over the one commodity that is a necessary ingredient for total domination: you.

By you, I mean you the individual in all your singular humanness.

Remaining singularly human and retaining your individuality and dominion over yourself—mind, body and soul—in the face of corporate and government technologies that aim to invade, intrude, monitor, manipulate and control us may be one of the greatest challenges before us.

These COVID-19 vaccines, which rely on messenger RNA technology that influences everything from viruses to memory, are merely the tipping point.

The groundwork being laid with these vaccines is a prologue to what will become the police state’s conquest of a new, relatively uncharted, frontier: inner space, specifically, the inner workings (genetic, biological, biometric, mental, emotional) of the human race.

If you were unnerved by the rapid deterioration of privacy under the Surveillance State, prepare to be terrified by the surveillance matrix that will be ushered in on the heels of the government’s rollout of this COVID-19 vaccine.

The term “matrix” was introduced into our cultural lexicon by the 1999 film The Matrix in which Neo, a computer programmer/hacker, awakens to the reality that humans have been enslaved by artificial intelligence and are being harvested for their bio-electrical energy.

Hardwired to a neuro-interactive simulation of reality called the “Matrix,” humans are kept inactive and docile while robotic androids gather the electricity their bodies generate. In order for the machines who run the Matrix to maintain control, they impose what appears to be a perfect world for humans to keep them distracted, content, and submissive.

Here’s the thing: Neo’s Matrix is not so far removed from our own technologically-hardwired worlds in which we’re increasingly beholden to corporate giants such as Google for powering so much of our lives. As journalist Ben Thompson explains:

Google+ is about unifying all of Google’s services under a single log-in which can be tracked across the Internet on every site that serves Google ads, uses Google sign-in, or utilizes Google analytics. Every feature of Google+—or of YouTube, or Maps, or Gmail, or any other service—is a flytrap meant to ensure you are logged in and being logged by Google at all times.

Everything we do is increasingly dependent on and, ultimately, controlled by our internet-connected, electronic devices. For example, in 2007, there were an estimated 10 million sensor devices connecting human utilized electronic devices (cell phones, laptops, etc.) to the Internet. By 2013, it had increased to 3.5 billion. By 2030, it is estimated to reach 100 trillion.

Much, if not all, of our electronic devices will be connected to Google, a neural network that approximates a massive global brain.

Google’s resources, beyond anything the world has ever seen, includes the huge data sets that result from one billion people using Google every single day and the Google knowledge graph “which consists of 800 million concepts and billions of relationships between them.”

The end goal? The creation of a new “human” species, so to speak, and the NSA, the Pentagon and the “Matrix” of surveillance agencies are part of the plan. As William Binney, one of the highest-level whistleblowers to ever emerge from the NSA, said, “The ultimate goal of the NSA is total population control.”

Mind you, this isn’t population control in the classic sense. It’s more about controlling the population through singularity, a marriage of sorts between machine and human beings in which artificial intelligence and the human brain will merge to form a superhuman mind.

“Google will know the answer to your question before you have asked it,” predicts transhumanist scientist Ray Kurzweil. “It will have read every email you’ve ever written, every document, every idle thought you’ve ever tapped into a search-engine box. It will know you better than your intimate partner does. Better, perhaps, than even yourself.”

The term “singularity”—that is, computers simulating human life itself—was coined years ago by mathematical geniuses Stanislaw Ulam and John von Neumann. “The ever accelerating progress of technology,” warned von Neumann, “gives the appearance of approaching some essential singularity in the history of the race beyond which human affairs, as we know them, could not continue.”

The plan is to develop a computer network that will exhibit intelligent behavior equivalent to or indistinguishable from that of human beings by 2029. And this goal is to have computers that will be “a billion times more powerful than all of the human brains on earth.”

Neuralink, a brain-computer chip interface (BCI), paves the way for AI control of the human brain, at which point the disconnect between humans and AI-controlled computers will become blurred and human minds and computers will essentially become one and the same. “In the most severe scenario, hacking a Neuralink-like device could turn ‘hosts’ into programmable drone armies capable of doing anything their ‘master’ wanted,” writes Jason Lau for Forbes.

Advances in neuroscience indicate that future behavior can be predicted based upon activity in certain portions of the brain, potentially creating a nightmare scenario in which government officials select certain segments of the population for more invasive surveillance or quarantine based solely upon their brain chemistry.

Case in point: researchers at the Mind Research Center scanned the brains of thousands of prison inmates in order to track their brain chemistry and their behavior after release. In one experiment, researchers determined that inmates with lower levels of activity in the area of the brain associated with error processing allegedly had a higher likelihood of committing a crime within four years of being released from prison. While researchers have cautioned against using the results of their research as a method of predicting future crime, it will undoubtedly become a focus of study for government officials.

There’s no limit to what can be accomplished—for good or ill—using brain-computer interfaces.

Researchers at Duke University Medical Center have created a brain-to-brain interface between lab rats, which allows them to transfer information directly between brains. In one particular experiment, researchers trained a rat to perform a task where it would hit a lever when lit. The trained rat then had its brain connected to an untrained rat’s brain via electrodes. The untrained rat was then able to learn the trained rat’s behavior via electrical stimulation. This even worked over great distances using the Internet, with a lab rat in North Carolina guiding the actions of a lab rat in Brazil.

Clearly, we are rapidly moving into the “posthuman era,” one in which humans will become a new type of being. “Technological devices,” writes journalist Marcelo Gleiser, “will be implanted in our heads and bodies, or used peripherally, like Google Glass, extending our senses and cognitive abilities.”

Transhumanism—the fusing of machines and people—is here to stay and will continue to grow.

In fact, as science and technology continue to advance, the ability to control humans will only increase. In 2014, for example, it was revealed that scientists have discovered how to deactivate that part of our brains that controls whether we are conscious or not. When researchers at George Washington University sent high frequency electrical signals to the claustrum—that thin sheet of neurons running between the left and right sides of the brain—their patients lost consciousness. Indeed, one patient started speaking more slowly until she became silent and still. When she regained consciousness, she had no memory of the event.

Add to this the fact that increasingly humans will be implanted with microchips for such benign purposes as tracking children or as medical devices to assist with our health. Such devices “point to an uber-surveillance society that is Big Brother on the inside looking out,” warns Dr. Katina Michael. “Governments or large corporations would have the ability to track people’s actions and movements, categorize them into different socio-economic, political, racial, or consumer groups and ultimately even control them.”

As I make clear in my book Battlefield America: The War on the American People, control is the issue.

In fact, Facebook and the Department of Defense are working to manipulate our behavior. In a 2012 study, Facebook tracked the emotional states of over 600,000 of its users. The goal of the study was to see if the emotions of users could be manipulated based upon whether they were fed positive or negative information in their news feeds. The conclusion of the study was that “emotional states can be transferred to others via emotional contagion, leading people to experience the same emotions without their awareness.”

All of this indicates a new path forward for large corporations and government entities that want to achieve absolute social control. Instead of relying solely on marauding SWAT teams and full-fledged surveillance apparatuses, they will work to manipulate our emotions to keep us in lock step with the American police state.

Now add this warp speed-deployed vaccine to that mix, with all of the associated unknown and fearsome possibilities for altering or controlling human epigenetics, and you start to see the perils inherent in blindly adopting emerging technologies without any restrictions in place to guard against technological tyranny and abuse.

It’s one thing for the starship Enterprise to boldly go where no man has gone before, but even Mr. Spock recognized the dangers of a world dominated by AI. “Computers make excellent and efficient servants,” he observed in “The Ultimate Computer” episode of Star Trek, “but I have no wish to serve under them.”




Under Guise of ‘Racial Justice,’ Johns Hopkins Lays Out Plan to Vaccinate Ethnic Minorities and Mentally Challenged First

Under Guise of ‘Racial Justice,’ Johns Hopkins Lays Out Plan to Vaccinate Ethnic Minorities and Mentally Challenged First
Claims made by Johns Hopkins Center for Health Security about its strategy for vaccinating ethnic minorities and the mentally challenged first, “as a matter of justice,” suggest ulterior motives.

by Jeremy Loffredo and  Whitney Webb
sourced from The Defender, Children’s Health Defense, December 1, 2020
originally published November 25, 2020 at Unlimited Hangout

 

With the first COVID-19 vaccine candidate set to receive an Emergency Use Authorization from the U.S. government in a matter of days, its distribution and allocation is set to begin “within 24 hours” of that vaccine’s imminent approval.

The allocation strategy of COVID-19 vaccines within the U.S. is set to dramatically differ from previous national vaccination programs. One key difference is that the vaccine effort itself, known as Operation Warp Speed, is being almost completely managed by the U.S. military, along with the Department of Homeland Security and the National Security Agency, as opposed to civilian health agencies, which are significantly less involved than previous national vaccination efforts and have even been barred from attending some Warp Speed meetings. In addition, for the first time since 2001, law enforcement officers and Department of Homeland Security officials are set to not be prioritized for early vaccination.

Another key difference is the plan to utilize a phased approach that targets “populations of focus” identified in advance by different government organizations, including the CDC’s Advisory Committee on Immunization Practices (ACIP). Characteristics of those “populations of focus,” also referred to as “critical populations” in official documentation, will then be identified by the secretive, Palantir-developed software tool known as “Tiberius” to guide Operation Warp Speed’s vaccine distribution efforts. Tiberius will provide Palantir access to sensitive health and demographic data of Americans, which the company will use to “help identify high-priority populations at highest risk of infection.”

This report is the first of a three-part series unmasking the racist components of the Pentagon-run project to both develop and distribute a COVID-19 vaccine. It explores the COVID-19 vaccine allocation strategy first outlined by the Johns Hopkins Center for Health Security and subsequent government allocation strategies that were informed by Johns Hopkins.

The main focus of this allocation strategy is to deliver vaccines first to racial minorities but in such a way as to make those minorities feel “at ease” and not like “guinea pigs” when receiving an experimental vaccine that those documents admit is likely to cause “certain adverse effects … more frequently in certain population subgroups.” Research has shown that those “subgroups” most at risk for adverse effects are these same minorities.

The documents also acknowledge that information warfare and economic coercion will likely be necessary to combat “vaccine hesitancy” among these minority groups. It even frames this clearly disproportionate focus on racial minorities as related to national concerns over “police brutality,” claiming that giving minorities the experimental vaccine first is necessary to combat “structural racism” and ensure “fairness and justice” in the healthcare system and society at large.

Part 2 of this series will discuss how Palantir, a company currently helping Department of Homeland Security and law enforcement violently target African Americans and Latinos, will be in charge of allocating “tailored” COVID-19 vaccines to those same minorities as well as Palantir’s origins and its executives’ views on race. Part 3 will explore the direct ties between a COVID-19 vaccine front-runner and the Eugenics Society, which was re-named the Galton Institute in 1989.

The planners

The Trump administration has been criticized for its rush to develop and deploy a COVID-19 vaccine and particularly for installing Monclef Slaoui, a former pharmaceutical executive with ongoing conflicts of interest, as chief scientific adviser for Operation Warp Speed, the Pentagon-run program to produce and distribute the vaccine. Yet, if and when a Biden administration takes power, Operation Warp Speed is set to proceed with little, if any, modification.

The Johns Hopkins Center for Health Security (CHS) director Tom Inglesby, who will serve on the Biden Health and Human Services (HHS) transition team, has praised Slaoui, telling Stat News that the longer someone like him can remain in charge of the nation’s COVID-19 vaccine effort, “the better it is for the country.”

Inglesby, who led discussions at the CHS’s Event 201 exercise in October 2019 and who was one of the primary authors of the controversial Johns Hopkins Dark Winter exercise in 2001, is emblematic of the U.S. government’s and the mainstream media’s general reliance on the Johns Hopkins Bloomberg School of Public Health (of which CHS is part) for pandemic-related matters. Slaoui regularly appears on network TV as a COVID-19 oracle and has been called “one of the nation’s go-to experts on the spread of the coronavirus.” Readers may note that the Johns Hopkins “coronavirus tracker” has been used by virtually every mainstream news source since the beginning of COVID-19 reporting. This relationship is expected to continue, if not intensify, in a Biden administration.

Both Kathleen Hicks, the lead on Biden’s Department of Defense (DOD) transition team, and Alexander Bick, on Biden’s National Security Council transition team, are scholars at Johns Hopkins Kissinger Center for Global Affairs, reflecting the university’s broader influence on a future Biden administration. Yet, the most significant way the Biden transition intersects with Johns Hopkins is through the CHS.

Originally called the Center for Civilian Biodefense Strategies, the CHS is a think tank within Johns Hopkins that regularly gives recommendations to both the U.S. government and the World Health Organization (WHO) and, like the Bill and Melinda Gates Foundation, has emerged as a voice of authority on all matters COVID-19 in the U.S. The center’s founding director was D. A. Henderson, best known for his role in the WHO-sponsored smallpox vaccination campaign. Henderson also held several government positions, including serving as associate director of the Office of Science and Technology Policy under George H. W. Bush. He was also the longtime dean of the Johns Hopkins School of Public Health.

Another member of the Biden transition team is Luciana Borio, a current member of the CHS steering committee. As both a former FDA scientist and former National Security Council member, Borio signifies the relationship between the national security state and the biosecurity state. She’s currently a vice president of In-Q-Tel, the venture-capital arm of the CIA.

In-Q-Tel’s current executive vice president, Tara O’Toole, who at the onset of the COVID-19 outbreak declared that “the best way ever to protect those who are well is with vaccines,” is Inglesby’s mentor and predecessor as director of the CHS. She was also a key player and the lead author of the CHS’s Dark Winter and CladeX bioterror simulations. The Engineering Contagion series published by The Last American Vagabond earlier this year explored the Dark Winter simulation in depth, including how the simulation eerily predicted the 2001 anthrax attacks that followed soon after September 11, 2001, with several participants demonstrating apparent foreknowledge of those attacks.

Ending racism with vaccines?

The Centers for Disease Control and Prevention (CDC) has consistently referenced materials developed by the CHS in its recent COVID-19 vaccine allocation literature. These CDC-issued materials form the backbone of the various vaccine allocation strategies issued by many state governments. Chief among these is the COVID-19 Vaccination Program Interim Playbook, published at the end of October. A key aspect of that program is the determination of “critical populations for COVID-19 vaccination, including those groups identified to receive the first available doses of COVID-19 vaccine when supply is expected to be limited.”

In August, the CHS published its Inglesby cowritten Interim Framework for COVID-19 Vaccine Allocation and Distribution, which is cited by the CDC as a key reference for its nationwide COVID-19 vaccine-allocation strategy. This report will examine this document, in particular, as well as other related documents that reveal that ethnic and racial minorities, specifically those over sixty-five and those who make up part of the “essential” workforce, are set to be the first to receive experimental COVID-19 vaccines.

The Interim Framework argues there is a need to prioritize ethnic minorities, particularly African Americans and Latino Americans, in order to reflect “fairness and justice.” It states that “a critical difference” between COVID-19 vaccine allocation and the “context envisioned in the 2018 guidance for pandemic influenza vaccine allocation” is the fact that the U.S. is “currently in the midst of a national reckoning on racial injustice, prompted by cases of police brutality and murder.” It goes on to state that “although structural racism was as present in the 2018 and previous influenza epidemics as it is today, the general public acknowledgment of racial injustice was not.”

It goes without saying that police brutality is decidedly unrelated to vaccine allocation as is increased national awareness of racial injustice as it relates to police brutality. This is further compounded by the police, in this document, being removed as a priority group for COVID-19 vaccine allocation, despite having been designated a priority group in all other government vaccine-allocation guidance since the 2001 anthrax attacks. Also odd is that it is only increased access of minorities to the COVID-19 vaccine that is cited as a way to address “structural racism in health systems,” not other policies that would be more likely to address the problem such as Medicare for All.

In addition, the Interim Framework admits that “communities of color, particularly Black populations, may be more wary of officials responsible for vaccine-related decisions due to past medical injustices committed by authorities on Black communities.” There is a long list of these “medical injustices” committed against minority communities by the U.S. government, including the infamous Tuskegee syphilis experiments, which are discussed in detail later.

Another odd passage on “justice” and “equity” as it relates to vaccinating ethnic minorities first states:

“In the context of vaccine allocation, treating individuals fairly has sometimes been defined as treating everyone the same or equally, for example, by distributing vaccines on a first-come, first-served basis or by giving everyone an equal chance at getting a vaccine via a lottery. Because the impact of the vaccine is different for different people (i.e., some people are at greater risk of death), the straightforward ways of treating people equally are often rejected as unfair or as an inefficient use of vaccine …

“In the context of vaccine allocation, promoting equity and social justice requires addressing higher rates of COVID-19–related severe illness and mortality among systematically disadvantaged or marginalized groups …

“As a matter of justice, these disparities in COVID-19 risk and adverse outcomes across racial and ethnic groups should be addressed in our overall COVID-19 response.”

This extreme emphasis on the “fairness and justice” of prioritizing minorities for the vaccine is contradicted by other claims made in the same document. For example, the document also states:

“The ultimate safety of an approved vaccine is not completely knowable until it has been administered to millions of people. During clinical trials, tens of thousands of individuals will receive the vaccine but that may fail to show safety concerns that occur with less frequency, such as 1 in a million. This can be a concern for particularly severe adverse effects.”

It also notes: “It is also possible that certain adverse effects may occur more frequently in certain population subgroups, which may not be apparent until millions are vaccinated.”

Notably, African Americans are understood to be at a higher risk for adverse reactions to vaccines. According to a study by the University of Pennsylvania, African Americans exhibit a disproportionately higher immune response to certain flu shots. And in 2014, the Mayo Clinic found that African Americans have almost double the immune response to the rubella vaccine as Caucasian Americans. Immune reactions that are too strong can result in more adverse events and inflammatory responses such as transverse myelitis, a debilitating inflammation and paralysis of the spinal cord. A 2010 study in the Journal of Toxicology and Environmental Health showed that African American boys were at significantly greater risk of suffering severe neurological injury from the hepatitis B shot as compared to Caucasians.

This raises the question as to whether African Americans should be prioritized for a poorly tested vaccine when the available science shows that this demographic may be at a higher risk for adverse reactions to vaccines. Previous coronavirus vaccine projects triggered immune responses so strong that the test animals died, and the vaccine projects got scrapped. The Johns Hopkins CHS Interim Framework claiming that vaccinating African Americans and other ethnic minorities first represents “fairness and justice” and would address “structural racism” does not square with its admission that the safety of the COVID-19 vaccine is “not completely knowable” until millions have received it and that “certain adverse effects may occur more frequently in certain population subgroups.”

Who is really to blame for ‘vaccine hesitancy’?

For a successful rollout of a COVID-19 vaccine, the federal government will need to reckon with “vaccine hesitancy,” which the WHO named as one of the top ten threats to global health in 2019 and which is a major concern discussed at length in the August Interim Framework on COVID-19 vaccination strategies.

According to recent polls, such hesitancy is, understandably, most prevalent among African Americans, the group that has most commonly been used as human guinea pigs by the U.S. government and associated scientific and medical institutions. For instance, there are the infamous Tuskegee University experiments, devised by the U.S. Public Health Service (now a division of HHS) and the CDC. The unwitting participants in the study, all of whom were African American, were told that they were receiving free health-care services from the federal government, while actually they were being intentionally untreated for syphilis so government scientists could study the devastating progression of the disease. Deception was critical to the experiment, as the participants did not know they were part of an experiment at all and were also kept unaware of their true diagnosis. While Tuskegee may be the most well-known example of racist medical experimentation in the U.S., it’s far from the only one.

For example, during the Manhattan Project, the undertaking that produced the atom bomb, the U.S. government contracted dozens of physicians to inject unknowing hospital patients with up to 4.7 micrograms of radioactive plutonium, forty-one times normal lifetime exposure. The goal of this experiment was to pinpoint the dosage at which radioactive elements such as plutonium would cause illnesses like leukemia, and to measure the amount of radioactivity that lingers in the blood, tissues, bones, and urine. Between 1944 and 1994 the Atomic Energy Commission supported thousands of experimental projects sanctioning such radiation on human subjects, most of whom were African Americans.

From 1954 to 1962, the Sloan-Kettering Institute, which receives hundreds of millions of dollars of NIH funds annually, injected over four hundred African American inmates at Ohio State Prison with live cancer cells to observe how the body might destroy them. The primary sponsor for this research was the National Institutes of Health, which also partially sponsored the Tuskegee experiments.

From 1987 through 1991, U.S. researchers administered as much as five hundred times the approved dosage of the Edmonton-Zagreb (EZ) measles vaccine to African American and Latino babies in low-income Los Angeles neighborhoods as part of a vaccine experiment. Consent forms did not inform parents of the increased dosage or of the fact that the vaccine was experimental. Parents were also not informed that the vaccine had already been given to 2,000 children in Haiti, Senegal, and Guinea-Bissau with disastrous results. For example, in Senegal, children who received the jab died at a rate  80% higher than children who did not receive it. The CDC would later characterize the U.S. trials as “clearly a mistake.”

Between 1992 and 1997, Columbia University’s Lowenstein Center for the Study and Prevention of Childhood Disruptive Behavior Disorders conducted studies that sought to establish a link between genetics and violence, focusing on minority children in New York City. These experiments targeted 126 boys between the ages of six and ten, 100% of whom were either African American, Latino, or biracial. In exchange for $100 and a $25 Toys “R” Us gift card, the children, selected because their older brothers had come into contact with the juvenile probation system, were taken from their homes, denied food and water, and given a drug called fenfluramine. Prior to these experiments, fenfluramine had never been administered to people under the age of twelve, and it was already known that the drug was associated with heart-valve damagebrain damage, and death.

Such historical facts raise obvious questions about the reasons for “vaccine hesitancy” and how they are currently being approached by the U.S. government and related institutions. While it would make the most sense to combat this problem by holding to account the people responsible for past abuses, such as those described above, the opposite has been the case. Instead, the CHS and other institutions, particularly regarding the coming COVID-19 vaccination campaign, have proposed several other means of combatting “vaccine hesitancy,” ranging from deception to information warfare to economic coercion.

A dark legacy poised to continue

Given the long-standing exploitive relationship between U.S. medicine and ethnic minorities, the August Interim Framework addresses the situation that communities of color, and in particular black populations, “may be more wary of officials responsible for vaccine-related decisions due to past medical injustices.” It states: “Anticipate hesitancy among marginalized populations who may be fearful or wary of seeking vaccination at sites that have historically caused mistrust.”

Another CHS paper, published in July, “The Public’s Role in COVID-19 Vaccination,” which is cited heavily in the August framework, acknowledged the U.S. “legacy of experimentation on Black men and women.”

However, the CHS document also notes that more than one COVID-19 vaccine candidate “may be available at the same time” and they “may have different safety and efficacy profiles across different population groups and may have different logistical requirements.” It adds that “it is also possible that certain adverse effects may occur more frequently in certain population subgroups, which may not be apparent until millions are vaccinated.”

It is notable that Palantir, the CIA-linked government technology contractor, has been put in charge of creating the software that will “decide” which “population subgroups” are given what vaccine. Palantir is perhaps best known for its controversial role in targeting undocumented immigrants through its contracts with ICE and its role in predictive-policing efforts that disproportionately targeted African Americans. It is certainly unsettling that those same ethnic groups that Palantir is most controversial for targeting on behalf of the national-security state and law enforcement are the same “critical populations” that the company will initially identify for the U.S. military–led COVID-19 vaccination program, Operation Warp Speed.

In addition, in a move that can only aggravate minority community “vaccine hesitancy,” the August CHS Interim Framework recommends that the CDC transform the current “vaccines adverse-event reporting system” from a voluntary system that relies on individuals sending in reports to the government to “an active surveillance system” that “monitors all vaccine recipients,” possibly via unspecified “electronic mechanisms.”

The Last American Vagabond reported last month that Operation Warp Speed, seemingly having taken a cue from the Interim Framework, plans to utilize “incredibly precise … tracking systems” that will “ensure that patients each get two doses of the same vaccine and to monitor them for adverse health effects.” Those systems will be managed, in part, by the intelligence-linked tech giants Google and Oracle.

The main stated purpose of these “tracking systems,” referred to in other Warp Speed documents as “pharmacovigilance systems,” is to monitor the longer-term effects of new, unlicensed vaccine-production methods that are being used in the production of every Warp Speed COVID-19 vaccine candidate. Per Warp Speed’s own documents, these methods “have limited previous data on safety in humans … the long-term safety of these vaccines will be carefully assessed using pharmacovigilance surveillance and Phase 4 (post-licensure) clinical trials,” following the administration of the COVID-19 vaccines to the prioritized “critical populations.”

A strategy takes shape

Given the above, the unprecedented facets of the Warp Speed COVID-19 vaccination plan — that is, its focus on ethnic minorities as the first to receive the experimental COVID-19 vaccine, its interest in giving different vaccine candidates to “different population groups,” and studying the largely unknown effects through “tracking systems” and unspecified “electronic mechanisms”— are all things that would obviously further fuel mistrust by those ethnic groups that have historically been targets of medical experimentation by the U.S. government.

Furthermore, that COVID-19 vaccine development and distribution efforts are being spearheaded by the military and national-security apparatus, as well as having the intimate involvement of controversial contractors such as Palantir, will likely exacerbate minority distrust as Operation Warp Speed advances, given that these same groups are those most often found to be on the receiving end of militarized state violence.

Also concerning is that law enforcement, military, and Department of Homeland Security officials will no longer be priority vaccine-allocation targets, for the first time since the 2001 anthrax attacks, while no convincing reason for their exclusion is offered.

Yet, instead of honestly addressing these unprecedented recommendations, the effort to get around the “vaccine hesitancy” issue as it relates to minorities plans to rely on tactics that avoid addressing any of these issues directly. In one example, although the August Interim Framework recommends “directly prioritizing” ethnic minorities, it recognizes that doing so “could further threaten the fragile trust that some have in the medical and public health system, particularly if there is the perception that there has been a lack of testing to assess vaccine safety and that they are the ‘guinea pigs.’” The document also states that “the implementation of directly prioritizing communities of color could also be challenging and divisive, as determining how to access specific populations and how to determine eligibility based on race or ethnicity includes many sensitive challenges.”

As a workaround for such concerns, the CHS suggests that “prioritizing other cohorts of the population, such as essential workers or those with underlying health conditions associated with poorer COVID-19 outcomes, could also indirectly help address the disproportionate burden of this pandemic on communities of color” due to the high representation of those minorities in the essential workforce.

The document continues: “While this approach might avoid some of the challenges outlined above, it would also need to be implemented in a way that ensures vaccines are equitably distributed across subcategories of these categories.” Thus, it suggests prioritizing “those individuals and groups who face both severe health and severe economic risks, specifically essential workers at higher risk of severe illness — or whose household members are at higher risk — who will suffer severe economic harm if they stop working.” Those groups at “higher risk of severe illness,” the document later notes, are incidentally ethnic minorities.

In other words, the strategy proposed by the CHS is to specifically prioritize cohorts of the U.S. population that contain high proportions of ethnic minorities without directly prioritizing those minorities in order to, somewhat deceptively, avoid exacerbating “vaccine hesitancy” concerns among those groups by directly singling them out.

The Interim Framework acknowledges the high prevalence of ethnic minorities in the essential workforce and cites a paper published in April 2020 by the Center for Economic and Policy Research that notes “people of color are overrepresented in many occupations with frontline industries.”

In addition to prioritizing essential workforce cohorts, which have a high percentage of ethnic minorities, the CHS document also suggests that prisoners, another group where ethnic minorities are heavily overrepresented, and “undocumented immigrant communities of color” should also be prioritized. Like the essential workforce strategy, this would ensure increased vaccine uptake by ethnic minorities without prioritizing them directly.

It is also worth noting that, in addition to the focus on ethnic minorities, the Interim Framework also recommends that “differently abled and mentally challenged populations, who can experience difficulties in accessing healthcare and could be in higher-risk living settings, such as assisted living facilities,” be included as a “target population” along with ethnic minorities.

This strategy as laid out by the CHS appears to have been embraced by the CDC’s ACIP, which is the official government body that will designate the “target populations” of the COVID-19 vaccination strategy.

Also in August, Kathleen Dooling, a CDC epidemiologist writing on behalf of ACIP’s COVID-19 Vaccines Work Group, stated that “groups for early phase vaccination” should be those that “overlap” the most with, first, those with “high risk” medical conditions, second, essential workers, and, third, adults over sixty-five. As previously noted, the essential workforce is predominantly composed of ethnic minorities.

Notably, the “high risk” medical conditions listed in this same document are conditions that are all significantly more prevalent among ethnic minorities, such as type 2 diabetesobesitychronic kidney diseaseserious heart conditions, and sickle cell disease. Cancer is also listed and, while prevalent across the U.S. population at large, the incidence of cancer is highest among African Americans.

Particularly notable is the inclusion of sickle cell disease, as African Americans in the U.S. have a much higher probability of having that condition than any other group. According to 2010 data analyzed by the CDC, the sickle cell gene, which is necessary in both parents for a child to inherit sickle cell disease, is present in 73 per 1,000 African American newborns, compared to three per 1,000 Caucasian newborns.

The “overlap” strategy fits with current CDC ACIP guidelines for vaccine recommendations, which hold that, if vaccination supply is limited, the CDC should “reduce the extra burden the disease is having on people already facing disparities.” The “overlap” strategy as laid out in the recent ACIP COVID-19 Vaccines Work Group document, however, has the inevitable end result of ensuring that the vast majority of those who will first receive the experimental COVID-19 vaccine will be ethnic minorities over the age of sixty-five and ethnic minorities in the essential workforce.

Also noteworthy in relation to the prioritization of ethnic minorities is that in March the government interpreted federal regulations to grant liability immunity to any entity producing, distributing, manufacturing, or administering COVID-19 countermeasures, including vaccines. According to HHS, this move may also “provide immunity from certain liability under civil rights laws,” meaning that those involved with the COVID-19 vaccination campaign may not be liable if found to violate the rights of groups protected under civil rights law, that is, ethnic minorities.

Controlling the narrative

Another tactic promoted by the CHS, as well as the CDC and Warp Speed, to combat “vaccine hesitancy” is aggressive communication strategies that include “saturating” the media landscape with provaccine content while greatly reducing content deemed to promote “vaccine hesitancy.” The national-security state, which is managing Operation Warp Speed, has become increasingly involved in this media effort, particularly by censoring content that is considered to be anti-vaccine (including, in their view, news outlets critical of the pharmaceutical industry and vaccine manufacturers) by using counterterror tools that have previously been used to disrupt online terrorist propaganda.

After the October 2019 coronavirus pandemic simulation, Event 201, the CHS issued a statement that media companies have a responsibility to ensure that “authoritative messages are prioritized.” The CHS had co-sponsored Event 201 alongside the World Economic Forum and the Bill and Melinda Gates Foundation.

There is much more to this information war than just the rapidly accelerating online censorship effort. For instance, the official Operation Warp Speed document “From the Factory to the Frontlines” notes that “strategic communications and public messaging are critical to ensure maximum acceptance of vaccines, requiring a saturation of messaging across the national media.” It also states that “working with established partners — especially those that are trusted sources for target audiences — is critical to advancing public understanding of, access to, and acceptance of eventual vaccines” and that “identifying the right messages to promote vaccine confidence, countering misinformation, and targeting outreach to vulnerable and at-risk populations will be necessary to achieve high coverage.”

The document also notes that Warp Speed will employ the CDC’s three-pronged strategic framework known as “Vaccinate with Confidence” for its communications thrust. The third pillar of that strategy is called “Stop Myths” and has as a main focus “establish[ing] partnerships to contain the spread of misinformation” as well as “work[ing] with local partners and trusted messengers to improve confidence in vaccines.”

Like the official Warp Speed guidance, the CDC Interim Framework also sees “community outreach” as an essential element for a successful vaccine campaign and suggests funding and training community health workers to promote vaccination specifically to “underserved, disproportionately affected groups.” It details how the U.S. government might engage African Americans, Latino Americans, and lower-income populations to build trust in connection with vaccine recommendations and get around “concerns that they are ‘testing subjects’ for a novel vaccine.”

The CHS document notes, for example, the importance of cultural competence when promoting vaccines, advising that vaccinating at “churches, schools, culturally specific community centers or senior centers” might sit better with marginalized populations and make them feel more at ease. Such considerations were further elaborated on by Luciana Borio in September. That month, the vice president of In-Q-Tel and member of Biden’s transition team, wrote that while it may be appropriate to use U.S. military resources for vaccination efforts, “any such federal engagement must be done in a collaborative manner sensitive to public perceptions that may be engendered by having a public health function fulfilled by individuals in uniform.”

A July CHS paper, “The Public’s Role in COVID-19 Vaccination,” a document Luciana Borio also helped write, argued, “Vaccination sites should not be heavily policed or send any signals that the site may be unsafe for Black or other minority communities.” This CHS paper further states that “trusted community spokespersons” should be utilized for a “communication campaign,” amplifying “vaccine-affirming, personally relevant messages.” Like similar WHO materials, it advocates tailoring the campaign to specific audiences and identifying a network of spokespeople to deliver a “salient and specific message repeatedly, delivered by multiple trusted messengers and via diverse media channels.”

The CDC also recommends vaccine administration at places such as university parking lots, soup kitchens, public libraries, and faith-based organizations. An October CDC report reads: “For people living in institutions, consider vaccination at intake; for people attending colleges/universities, vaccinate at enrollment.” It also proposes that U.S. states and territories utilize nontraditional vaccination sites such as homeless shelters and food pantries.

The prospect of red-carpet celebrities, influencers, and “trusted messengers” endorsing public-health policy is not unthinkable. According to NBC New York, New York and New Jersey have already recruited celebrities to urge residents to follow CDC guidelines. Actors including Julia Roberts, Penelope Cruz, Sarah Jessica Parker, Robin Wright, and Hugh Jackman earlier this year joined a coordinated campaign to “pass the mic to COVID-19 experts.”

In addition, this summer the WHO paid PR firm Hill & Knowlton Strategies $135,000 to identify micro-influencers, macro-influencers, and what it calls “hidden heroes” who “shape and guide conversations” to promote WHO messaging on social media and promote the organization’s image as a COVID-19 authority. Hill & Knowlton are controversial for having previously manufactured the false “incubator baby” testimony delivered in front of Congress that propelled the U.S. into the first Gulf War in the early 1990s.

The Public’s Role in COVID-19 Vaccination” also urges using groups such as faith-based organizations, schools, homeowners’ associations, and unions trusted by “hard-to-reach audiences” to convey positive vaccine messages and to “modulate public perceptions of vaccination.” Accordingly, the July CHS paper notes “the importance of using outside groups who have relationships with the community, instead of direct government involvement.” It should be noted that during the Tuskegee experiments, the U.S. Public Health Service hired Eunice Rivers, a black nurse with a close relationship to the local minority community, to maintain contact with those who were part of the experiment to ensure they continued to participate.

This outsourcing framework as laid out by the CHS is reproduced in the federal government’s own literature. An October CDC report, Interim Playbook for Jurisdiction Operations, describes the importance of engaging what minority populations would consider “trusted sources” such as union representatives, college presidents, athletic coaches, state licensure boards, homeless shelter staff, soup kitchen managers, and faith leaders to “address hesitancy” in relation to the COVID-19 vaccine.

Operation Warp Speed’s document “From the Factory to the Frontlines,” released the same day as the CDC Interim Playbook, gives more specific examples of the government’s ongoing work with organizations “representing minority populations,” stating that faith-based organizations can be critical. “HHS’s Center for Faith and Opportunity Initiatives is working with minority-serving faith and community groups … and encouraging participation in the vaccination program,” the document reads. It also states that an “information campaign” led by HHS’s public affairs department is already working to “target key populations and communities to ensure maximum vaccine acceptance.”

Of note is that a member of Biden’s Office of Management and Budget (OMB) transition team is Bridget Dooling. The OMB houses the Office of Information and Regulatory Affairs, which reviews all regulations across the federal government. Dooling previously worked at OIRA, and from 2009 until 2011 worked under the direction of then-OIRA administrator Cass Sunstein. On Twitter, Dooling regularly interacts with Sunstein. She has frequently promoted Sunstein’s work on Twitter, especially this past month.

Notably, in 2008, Sunstein authored a paper encouraging the U.S. government to employ covert agents to “cognitively infiltrate” online dissident groups that promote antigovernment “conspiracy theories” and to maintain a vigorous “counter misinformation establishment.”

Elements of his strategy for tackling anti-government “conspiracy theories” are analogous to the aforementioned CHS theme of using “outside groups who have relationships with the community” instead of the government directly. “Governments can supply these independent bodies with information and perhaps prod them into action from behind the scenes,” he contended in his paper.

Sunstein was recently made chair of the World Health Organization’s Technical Advisory Group on Behavioral Insights and Sciences for Health to ensure “vaccine acceptance and uptake in the context of COVID-19.”

In September he also wrote an opinion piece for Bloomberg, “How to Fight Back against Coronavirus Vaccine Phobia,” suggesting that “high-profile people who are respected and admired by those who lack confidence in vaccines” will help sell the public on the safety of vaccines. “Trusted politicians, athletes or actors — thought to be ‘one of us’ rather than ‘one of them’ — might explicitly endorse vaccination,” he writes.

When all else fails, coerce

In addition to this information warfare approach to combating “vaccine hesitancy,” the government also intends to stave off possible hesitancy through economic coercion, that is, by using economic incentives, even linking vaccination to entrance into the workforce, housing assistance, food, travel, and education.

Sunstein’s Bloomberg piece, for example, states that when a vaccine is available, “an economic incentive, such as a small gift certificate, can help” make it easy for “people who are at particular risk. Such gift cards will inevitably be more effective at swaying decisions of the poor.”

Former 2020 Presidential Candidate and U.S. Representative for Maryland’s 6th congressional district John Delaney recently penned an article in the Washington Post, “Pay Americans to Take a Coronavirus Vaccine,” in which he argues a way to overcome the “historical level of distrust” in the vaccine development process is to take advantage of the current economic crisis and “pay people to take a COVID vaccine.” Delaney writes, “Such an incentive might be the most effective way to persuade people to overcome suspicion or even fear …”

CHS’s “The Public’s Role in COVID-19 Vaccination,” paper also details how bundling services like “food security, rent assistance, [and] free clinic services” with vaccination can increase vaccine intake. “Local and state public health agencies should explore opportunities to bundle COVID-19 vaccination with other safety net services,” it suggests. One way of doing this is to simply provide “food aid, employment aid, or other preventative health services” that “may be urgently needed” at vaccination sites. “[And] in some cases,” says the CHS, “it also may be acceptable and feasible to deliver vaccination via home visits by community health nurses when vaccination is bundled with delivery of other services.”

This strategy for increasing vaccine intake parallels what the CHS proposes in order to make digital contact tracing technology (DCTT) widespread in the population without mandating it outright. “Instead of making use fully voluntary and initiated by users, there are ways that DCTT could be put into use without users’ voluntary choice,” a recent CHS paper “Digital Contact Tracing for Pandemic Response” reads. It continues: “For example, use of an app could be mandated as a precondition for returning to work or school, or even further, to control entry into a facility or transportation (such as airplanes) through scanning of a QR code.”

Palantir and priority populations

Aside from the troubling aspects of the COVID-19 vaccination strategy as outlined above, there is the separate issue of the way in which these “populations of focus” will be chosen and identified. Palantir, the big data firm with deep and persisting ties to the CIA, has created a new software tool expressly for Warp Speed called Tiberius. Not only will Tiberius use Palantir’s Gotham software and its artificial intelligence components to “help identify high-priority populations,” it will produce delivery timetables and map out the locations for vaccine distribution based on the masses of data it has collected through various contracts with HHS and data-sharing alliances with In-Q-Tel, Amazon, Google and Microsoft, among others.

These data include extremely sensitive information about American citizens and the lack of privacy safeguards governing Palantir’s growing access to American healthcare data has even gotten the attention of Congress, with several senators and representatives warning in July that Palantir’s massive stores of data “could be used by other federal agencies in unexpected, unregulated, and potentially harmful ways, such as in the law and immigration enforcement context.”

Given that Palantir, at present, is best known for targeting the same minorities that are slated to be “priority populations” for early receipt of the experimental COVID-19 vaccine, Tiberius and the company behind it, including the obsessive “race war” fears of its top executive, will be explored in Part 2 of this series.


Jeremy Loffredo is a reporter for The Defender.




Johns Hopkins Study Explodes COVID Death Hoax; It’s Re-Labeling on a Grand Scale

Johns Hopkins Study Explodes COVID Death Hoax; It’s Re-Labeling on a Grand Scale
“This patient who died had an ordinary heart attack.”
“Not anymore. We’re repackaging it as COVID.”

 

by Jon Rappoport, No More Fake News
November 30, 2020

 

Don’t blink. Johns Hopkins may delete or retract their analysis at any moment. Their author’s study is devastating. Too hot to handle.

UPDATE: Yes, I wrote that opener a few hours before Johns Hopkins stepped in and DID retract the article. Boom. [1] [2] [3] [4]

Hopkins claims the article has been used to spread misinformation about the pandemic, and contains factual errors. CDC is cited as one correct source of facts. Hmm.

Regardless, here is my article, finished before the Johns Hopkins retraction. Since then, I’ve only polished it a bit in several places, for clarity:

Months ago, I told you this, in a number of articles: The overwhelming percentage of people who are “dying from the virus” are actually dying from traditional diseases.

These people have been relabeled and repackaged as “COVID-19.”

It has nothing to do with “the virus.”

A new analysis from Johns Hopkins confirms this in spades.

The Johns Hopkins News-Letter article, in a student publication, is headlined, “A closer look at US deaths due to COVID-19.” It lays out the case made by “Genevieve Briand, assistant program director of the Applied Economics master’s degree program at Hopkins.”

As you keep reading, keep this in mind: If the so-called increase in mortality from COVID is offset, almost exactly, by a decrease in deaths from all other major diseases…

Indicating that the so-called COVID deaths are nothing more than an exercise in re-labeling, then…

You can say there is a new coronavirus, but it’s even less harmful than flu, because virtually everybody recovers…

Or you can say the whole story of a new coronavirus is a fake narrative. There is no new virus.

My readers know I’ve been offering much evidence for the latter conclusion.

Here are key quotes from the Johns Hopkins News-Letter article:

“These data analyses suggest that in contrast to most people’s assumptions, the number of deaths by COVID-19 is not alarming. In fact, it has relatively no effect on deaths in the United States.”

“This comes as a shock to many people. How is it that the data lie so far from our perception?”

“When Briand looked at the 2020 data during that seasonal period, COVID-19-related deaths exceeded deaths from heart diseases. This was highly unusual since heart disease has always prevailed as the leading cause of deaths. However, when taking a closer look at the death numbers, she noted something strange. As Briand compared the number of deaths per cause during that period in 2020 to [deaths per cause in] 2018, she noticed that instead of the expected drastic increase across all causes, there was a significant decrease in deaths due to heart disease. Even more surprising, as seen in the graph below, this sudden decline in deaths is observed for all other causes.”

“This trend is completely contrary to the pattern observed in all previous years. Interestingly, as depicted in the table below, the total decrease in deaths by other causes almost exactly equals the increase in deaths by COVID-19. This suggests, according to Briand, that the COVID-19 death toll is misleading. Briand believes that deaths due to heart diseases, respiratory diseases, influenza and pneumonia may instead be [may have been] recategorized as being due to COVID-19.”

“The CDC classified all deaths that are related to COVID-19 simply as COVID-19 deaths. Even patients dying from other underlying diseases but are infected with COVID-19 count as COVID-19 deaths. This is likely the main explanation as to why COVID-19 deaths drastically increased while deaths by all other diseases experienced a significant decrease.”

“’All of this points to no evidence that COVID-19 created any excess deaths. Total death numbers are not above normal death numbers. We found no evidence to the contrary,’ Briand concluded.”

“’If [the COVID-19 death toll] was not misleading at all, what we should have observed is an increased number of heart attacks and increased COVID-19 numbers. But a decreased number of heart attacks and all the other death causes doesn’t give us a choice but to point to some misclassification [re-labeling],’ Briand replied.”

“In other words, the effect of COVID-19 on deaths in the U.S. is considered problematic only when it increases the total number of deaths or the true death burden by a significant amount in addition to the expected deaths by other causes. Since the crude number of total deaths by all causes before and after COVID-19 [was first announced] has stayed the same, one can hardly say, in Briand’s view, that COVID-19 deaths are concerning.”

Of course, there is some mealy-mouthed backtracking in the article. The virus is deadly and the pandemic is real, etc. But the data are the data.

The whole COVID operation is a hoax.

If I thought other honest researchers would investigate and re-calculate the Hopkins analysis, I would say, let’s see what they come up with. But based on my experience, there will be, at best, a brief flurry of articles in the press about this extraordinary finding, and then the scientific and press denizens will move on, as if nothing happened. That is their way. They briefly expose a scandal and then they slither off to cover up the scandal.

The other possibility is: Hopkins will retract the analysis, claiming it was flawed. That is the other strategy the low-crawling creatures sometimes deploy.

So there you have it.

Hoax. Con. Fake.

As I keep reporting, the virus (never proven to exist) is the cover story for the true phase-one goal: destruction of the economy.

If the virus were real, if it were attacking people left and right, the all-cause mortality numbers would be through the roof.

But they aren’t.

“I have a great idea, Bill. Let’s declare a fake pandemic. We’ll report all sorts of high death numbers. But really, we’ll just be subtracting numbers from other traditional diseases that cause deaths, and we’ll add those numbers to our fake pandemic.”

“Sounds great, Tony. Can you pull it off? I mean, it’s pretty obvious.”

“Sure, we can pull it off. And if some journalist with a mainstream reputation or an institution suddenly develops a brief infection of ETHICS, we’ll call their work a mistake or a lapse in judgment.”

“You mean an institution like the World Health Organization or Johns Hopkins?”

“Right. We’ll say the institution didn’t issue the study, it was just one of their people, a lone researcher. And if necessary, the institution, under pressure, will back off. But that’s assuming anyone noticed the study in the first place. Normally, these ‘revelations’ surface for a moment and then sink like a stone. No one cares. A pandemic is a money waterfall. The beneficiaries won’t sacrifice their bottom lines, or their reputations…”

Of course, people can rise up and raise holy hell.


SOURCES:

[1] https://www.jhunewsletter.com/article/2020/11/a-closer-look-at-u-s-deaths-due-to-covid-19

[2] https://web.archive.org/web/20201126163323/https://www.jhunewsletter.com/article/2020/11/a-closer-look-at-u-s-deaths-due-to-covid-19

[3] https://drive.google.com/file/d/1iO0K75EZAF8dkNDkDmM3L4zNNY0X-Xw5/view

[4] https://www.youtube.com/watch?v=3TKJN61aflI




Police for Freedom: Spanish Police Rise Up Against “Covid” Lies & Mandates — Saying No to Masks, Forced Vaccines & Crimes Against Humanity

Police for Freedom: Spanish Police Rise Up Against “Covid” Lies & Mandates — Saying No to Masks, Forced Vaccines & Crimes Against Humanity

 

Marching with Policias por la Libertad in Valencia 

by Dawn of Peace
November 30, 2020

 



Original video is available at Dawn of Peace YouTube channel.

An amazing movement is beginning to take form in Spain as a group of police has come together to blow the whistle on the systemic human rights abuse and take a stand for freedom.

On the 28th of November, Policías por la Libertad (Police for Freedom) were leading the peaceful march through Valencia, supported by Dawn of Peace, Doctors for Truth, Scientists for Truth, Firemen for Freedom and Truth, Soberanía y Salud as well as Rebelión en La Granja.

We are coming together and standing on the right side of history! Join us!

Contact the groups here:
Policías por la Libertad : https://www.policiasporlalibertad.org
Dawn of Peace : https://dawnofpeace.org
Medicos por la Verdad : https://medicosporlaverdad.es
Soberanía y Salud : https://soberaniaysalud.com/ https://soberaniaysalud.com/
Rebelión en La Granja : https://t.me/ReVelionenlagranja
Difusión Josep Pamies : https://t.me/BoticaBerde

 



See Related:

‘Police for Freedom’: Spanish Officers Demonstrate Against the Coronavirus Lockdown and Masks

by Amy Mek, RAIR Foundation USA
November 30, 2020

 

On November 28, 2020, “Police for Freedom” a group comprised of Spanish Law Enforcement officers, held a demonstration in the streets of downtown Valencia, Spain. The officers are protesting against their socialist government’s management of the Chinese coronavirus, the violation of citizens freedoms, and the mandated mask measures.

The demonstrators held signs declaring, “Enough with the Lies, “Enough with the Human Rights Abuse”, “The police want to breathe”, and “No to the Vaccine”.

“Police for Freedom” is a recently formed group that brings together members of State Security Forces and private surveillance groups to ensure the rights of Spanish citizens are protected. This same patriotic group held a large march in Madrid on November 7.

The groups spokesperson Sonia Vescovacci, a national police officer on leave of absence, has called for the civil liberties of citizens to be respected. Vescovacci has encouraged her fellow officers to fail to comply with the government tyrannical orders to punish people who do not use masks or deny the seriousness of the pandemic.

Although the group instructed all participants to wear masks, a large portion of the demonstrators did not listen to their request. Following the rally, Valencia’s local government targeted police, the event organizers and participants for failing to comply with the states coronavirus measures. Ninety police officers have received fines for demonstrating against the “Imposition of masks” without wearing them.

Read More Here

 




The Strangely Unscientific Masking of America

The Strangely Unscientific Masking of America

by Jenin Younes, American Institute for Economic Research
November 27, 2020

 

I remember vividly the day, at the tail end of March, when facemasks suddenly became synonymous with morality: either one cared about the lives of others and donned a mask, or one was selfish and refused to do so. The shift occurred virtually overnight.

Only a day or two before, I had associated this attire solely with surgeons and people living in heavily polluted regions. Now, my friends’ favorite pastime during our weekly Zoom sessions was excoriating people for running or socializing without masks in Prospect Park. I was mystified by their certitude that bits of cloth were the only thing standing between us and mass death, particularly when mere weeks prior, the message from medical experts contradicted this new doctrine.

On February 29, the U.S. surgeon general infamously tweeted: “Seriously people – STOP BUYING MASKS. . . They are NOT effective in preventing general public from catching #Coronavirus.” Anthony Fauci, the best-known member of the coronavirus task force, advised Americans not to wear masks around this time. Similarly, in the earliest weeks of the pandemic, the CDC maintained that masks should be worn only by individuals who were symptomatic or caring for a sick person, a position that the WHO stood by even longer.

As rapidly as mask use became a matter of ethics, the issue transformed into a political one, exemplified by an article printed on March 27 in the New York Times, entitled “More Americans Should Probably Wear Masks for Protection.” The piece was heavy on fear-mongering and light on evidence.  While acknowledging that “[t]here is very little data showing that flat surgical masks, in particular, have a protective effect for the general public,” the author went on to argue that they “may be better than nothing,” and cited a couple of studies in which surgical masks ostensibly reduced influenza transmission rates.

One report reached its conclusion based on observations of a “dummy head attached to a breathing simulator.”  Another analyzed use of surgical masks on people experiencing at least two symptoms of acute respiratory illness. Incidentally, not one of these studies involved cloth masks or accounted for real-world mask usage (or misusage) among lay people, and none established efficacy of widespread mask-wearing by people not exhibiting symptoms.  There was simply no evidence whatsoever that healthy people ought to wear masks when going about their lives, especially outdoors.  Yet by April, to walk the streets of Brooklyn with one’s nose and mouth exposed evoked the sort of reaction that in February would have been reserved for the appearance of a machine gun.

In short order, the politicization intensified. President Trump refused to wear a mask relatively early on, so resistance to them was equated with support for him. By the same token, Democratic politicians across the board eagerly adopted the garb; accordingly, all good liberals were wearing masks religiously by the beginning of April. Likewise, left-leaning newspapers such as the New York Times and the Washington Post unequivocally promoted mask-wearing after that March 27 article, with no real analysis or consideration of opposing views and evidence.

The speed with which mask-wearing among the general public transitioned from unheard of to a moral necessity struck me as suspicious. After all, if the science was as airtight as those around me claimed, surely masks would have been recommended by January or February, not to mention during prior infectious disease outbreaks such as the 2009 swine flu. It seemed unlikely that the scientific proof became incontrovertible sometime between late February and late March, particularly in the absence of any new evidence surfacing during that time period.

Perhaps none of this is particularly surprising in this hyper-political era. What is shocking is the scientific community’s participation in subverting evidence that does not comport with the consensus. A prime example is the Institute of Health Metrics Evaluation’s (“IHME”) rather astounding claim, published in the journal Nature-Medicine and echoed in countless articles afterward, that the lives of 130,000 people could be saved with a nationwide mask mandate.

As my colleague Phil Magness pointed out in an op-ed in the Wall Street Journal, the IHME model was predicated upon faulty data:  it assumed that 49% of Americans were wearing masks based on a survey conducted between April and June, while claiming that statistic represented the number of Americans wearing masks as of September 21.  In fact, by the summer, around 80% of Americans were regularly wearing them.  (Ironically, had Dr. Fauci and the Surgeon General not bungled the message in March, mask use probably would have reached much higher rates much earlier on).

This called into question the accuracy of the 130,000 figure, since many more people habitually used masks than the study presumed.

Although Magness contacted Nature-Medicine to point out the problem, after stalling for nearly two weeks, the journal declined to address it.  Needless to say, the damage had been done:  newspapers such as the New York Times undoubtedly would fail to correct the error and any retractions certainly would be placed far from the front page, where the initial article touting the IHME figure appeared. Thus, as expected, the unfounded claim that 130,000 lives could be saved with a nationwide mask-mandate continues to be repeated, including by president-elect Joe Biden and National Institutes of Health Director Francis Collins.

That the science behind mask-wearing is questionable at best is further exemplified by a letter to the editor written in response to Magness’s article. Dr. Christopher Murray acknowledged that rates of mask-wearing have steadily increased, but then concluded that masks should be used because they are “our first line of defense against the pandemic” and current IHME modeling indicates that “if 95% of U.S. residents were to wear masks when leaving home, we could prevent the deaths of tens of thousands of Americans” because “masks work,” and “much deeper pain is ahead if we refuse to wear them.”

None of this accounts for the failure of either Nature-Medicine or the IHME modelers to recognize and correct the error.  Moreover, neither the IHME modelers nor Dr. Murray provide any evidence that masks work. They assume masks are extremely effective at preventing spread of the coronavirus, and then claim that the model is correct for that reason. This sort of circular reasoning is all-too typical of those who so vociferously insist that masks are effective without going to the trouble of substantiating that contention – or differentiating what is likely a modest benefit from mask-wearing in specific indoor locations and around high-risk individuals from the media-driven tendency to depict masks as a silver bullet for stopping the virus in all circumstances.

Coverage of a recent mask study conducted in Denmark likewise epitomizes the failure of the scientific community to rigorously engage with results that do not fit the prevailing masks-as-a-panacea narrative. The first randomized and controlled study of its kind (another appeared in May but it pertained to flu and had similar results), it found an absence of empirical evidence that masks provide protection to people wearing them, although it apparently did not assess whether they prevent infection of those who encounter the wearer.  The report was covered in a New York Times article bearing the patronizing headline, “A New Study Questions Whether Masks Protect Wearers. You Need to Wear Them Anyway.”

Noting that the results “conflict with those from a number of other studies,” primarily “laboratory examinations of the particles blocked by materials of various types,” the author remarked that, therefore, this research “is not likely to alter public health recommendations in the United States.” Notably, laboratory examinations, as opposed to the Danish study, do not account for the realities of everyday mask usage by non-medical professionals.

The author then quotes Susan Ellenberg, a biostatistician at the University of Pennsylvania, who claims that the study indicates a trend: “‘in the direction of benefit’ even if the results were not statistically significant. ‘Nothing in this study suggests . . . that it is useless to wear a mask,’” according to Dr. Ellenberg.

Nor does anything in this study suggest that it is useful to wear a mask, a fact that Dr. Ellenberg (and the headline) conveniently ignores. Furthermore, if a result is statistically insignificant, it should not be used to make the case for any proposition — as even I, a layperson, know.

Scientists ought to dispassionately analyze data that contradicts their biases and assumptions, and be open to changing their beliefs accordingly. That the results of the only randomized, controlled study were and continue to be automatically discounted demonstrates that, when it comes to the subject of masks, anything approximating the scientific method has gone out the window. That is all the more evident given the lack of interest that mask proponents have shown in conducting a randomized, controlled study themselves.

An article in the Los Angeles Times went even further: it twisted the findings of the Danish study to argue, incomprehensibly, that the research demonstrated more mask-wearing is warranted.  The author cited, as supposedly compelling evidence that masks work, the low Covid-19 death rates in Singapore, Vietnam, and Taiwan.  Indeed, according to the latest YouGov poll, administered in mid-November, 83% of Americans now wear masks in public, higher rates than Vietnam (77%) and Taiwan (82%).

Furthermore, there are other explanations, apart from widespread mask usage, for the remarkably low death rates in these countries.   Some scientists believe that previous exposure to other coronaviruses in these regions may confer partial or total immunity to SARS-CoV-2. Others have speculated that obesity, environment or genetics could be the reason that Europe and the United States have substantially higher death rates than many Asian and African countries; after all, obesity is one of the most significant risk factors for severe illness.

To conclude on the basis of low death rates in several countries that masks prevent coronavirus transmission is patently absurd, illogical, and unscientific. A casual observer might also note that coronavirus cases (albeit not necessarily deaths) are rising in many parts of the world, regardless of mask mandates or rates of implementation. While not a controlled experiment, this fact at least ought to be addressed when making such sweeping claims.

Ultimately, I do not have the credentials to determine whether or not –or to what extent — masks work. But it is obvious that the issue has become so politicized that mainstream media outlets, politicians, and even scientists seize upon the slightest bit of favorable evidence, dismiss out of hand anything that conflicts with their theory, and most egregiously of all misrepresent the data, to support the conclusion that masks worn by asymptomatic people prevent coronavirus transmission.

And masks are only one part of this story: school closures, lockdowns, and social distancing all have been dogmatically embraced as a means of controlling infection. The substantial evidence that these mechanisms are not effective, particularly beyond their duration, has been automatically rejected for too long. This is not science: it is politics, and those within the profession who have refused to examine their confirmation biases, or manipulated the evidence to score political points, are utterly unqualified for the job.

 



Jenin Younes is a public defender in New York City. She enjoys running, restaurants, and reading in her free time.

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Attorney Dr. Reiner Fuellmich: 1st of Many Lawsuits Has Been Filed to Attack Use of PCR Tests Which Are the Cornerstone of “Crimes Against Humanity” Crisis

Attorney Dr. Reiner Fuellmich: 1st of Many Lawsuits Has Been Filed to Attack Use of PCR Tests Which Are the Cornerstone of “Crimes Against Humanity” Crisis

by Dr. Reiner Fuellmich
November 25, 2020
this is an excerpt from Ben Swann’s RT podcast

 



Original video is available at Dr. Reiner Fuellmich YouTube channel.

[As a service to protect truth from censorship & to share widely, mirrored copies of this video are available at Truth Comes to Light BitChute, Brighteon, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]




Will The Shots Be Mandatory?

Will The Shots Be Mandatory?

by Jefferey Jaxen, The HighWire
November 24, 2020

 

Throughout the coronavirus response, those within ‘official’ positions around the world have chimed in on the idea of a mandatory Covid shot. Their hopes and potential future plans have been all over the board causing apprehension and confusion within the public. Whether you want the eventual shot, being rushed through emergency use authorization, or not, answers have not been clear.

In what has been a growing trend in political, and now health reporting, shadowy anonymous sources have driven headlines and news cycles. Always framed as ‘for their protection,’ yet ignoring accuracy or ability to verify their prognostications, the vaccine narrative hasn’t escaped it.

CNBC is now reporting that “The Food and Drug Administration has asked a group of advisors to set aside three days in early December for potential meetings to discuss Covid-19 vaccines…according to two people familiar with the plans. The advisory group may be asked to weigh in on Pfizer and Moderna’s vaccines, said the people, who asked not to be named because the plans aren’t yet public.”

Biden gave his answers in October during an ABC News Town Hall saying “we should be thinking about making it mandatory.” When asked how he would enforce that, Biden appeared to describe a scenario where he would ask Governors and mayors to execute the mandates.

Anyone paying attention to the last few years of American legislation sweeping across states [originally justified due to a measles outbreak] will easily see how such mandates will roll out. They will take the form of coercion by law, threatening to take away anything from access to school [for children] and daycare all the way to unemployment benefits for adults. Meanwhile, grocery stores, travel, and concert venues have already signaled they are open to denying access unless proof of vaccination is shown.

Frontline workers are being targeted for the first round of the Covid shots. It will be no surprise if hospitals treat their previously celebrated frontline heroes like subhuman rule-violators if they refuse the experimental shot.

Tests cases have already proven themselves in thorough court settings when it came to mandatory flu shots for healthcare workers. The “vaccinate or mask” policy was ruled unreasonable and called “a coercive tool” instead of a protective health policy in a case brought against the Sault Area Hospital in Sault Ste. Marie.

Nevertheless, the medical community, whose aggressively protected dictum of lauding the safety and efficacy of vaccination when doling them out to kids, are now suddenly questioning the coming shots they’ll be coerced into taking. Or through the lens of the mainstream media’s open discriminatory stance, the medical community has turned into ‘anti-vaxxers.’

A Facebook group titled NHS Workers for Choice, No Restrictions for Declining a Vaccine insist they are not an anti-vaccine – but that didn’t stop the media from calling them names. The group was made up of “hundreds of NHS staff” including “a GP, several A&E nurses, healthcare assistants, lab workers, and care home staff” according to the Daily Star hit piece.

Meanwhile, here in the U.S. the Washington Post spins their coverage a little gentler with its piece titled Doctors and nurses want more data before championing vaccines to end the pandemic. WaPo writes of a propaganda push when describing “Large health systems, medical societies and the federal government are launching an effort to persuade front-line health-care providers to take novel vaccines.”

The endless hype surrounding the endpoint data from Pfizer, Moderna and AstraZeneca’s shot is not thorough at this stage, published in peer-reviewed journals or even transparent for the public to access. It’s from simple science by press release public relations statements. In addition, the data being submitted for Emergency Use Authorization to the FDA is often resting on a small number of the total participants involved in the trials.

Speaking to the matter, vaccine safety scientist and infectious diseases physician Rebecca Chandler wrote:

“Perhaps watching a scientific community praise and promote vaccines based on press releases rather than review of data may actually promote vaccine skepticism.”

The hesitancy among doctors and nurses is not the same as the anti-vaccine movement, writes the WaPo who appear to be correct. Traditionally, what the media labels ‘anti-vaxxers’ were parents who were ‘pro-vax’ until experiencing an injury in their child after following recommended schedules put forth by officials. In juxtaposition, the WaPo writes of New Jersey State doctors “Among professionals contacted by the state, “some did not want to be in the first round, so they could wait and see if there are potential side effects,” New Jersey Health Commissioner Judith M. Persichilli said at a Nov. 9 news briefing. Of those who said they would not take the vaccine, many said they would be more than willing to get the vaccine at a later date, when more data is available,” she said.” It appears those doctors are going to wait around and see if the people they inject will show adverse reactions before deciding to take the shot themselves.

A survey of 609 healthcare workers in Los Angeles found respondents reported unwillingness to participate in a coronavirus vaccine trial, with 66.5% intending to delay vaccination.

Over the last month, headlines abound intending to shape the public narrative around the coming Covid shot. Global News Canada asks A coronavirus vaccine is almost ready. But will you take it? Forbes tells you What The Public Thinks About Mandatory Covid-19 Vaccinations. 

Some within government are already taking counter-actions.Florida state Rep. Anthony Sabatini took to Twitter writing:

Florida Gov. DeSantis stated regarding the hyped press releases from Covid vaccine-makers hype, “I do believe that these breakthroughs represent probably the greatest rays of hope that we have seen since the pandemic began,”

Gov. DeSantis stated that Florida residents will not be mandated to take either vaccine.

While states are also now chiming in about how they will handle getting the shot into the arms of their residents. Law.com writes, “The New York State Bar Association on Saturday passed a resolution urging the state to consider making it mandatory for all New Yorkers to undergo COVID-19 vaccination when a vaccine becomes available, even if people object to it for “religious, philosophical or personal reasons.

Regarding the kids, government contractor Dr. Moncef Slaoui said in a recent interview, “the plan is to run trials at an expedited pace over the coming months, first with younger adolescents, then toddlers, and, finally, infants. If that goes well, Slaoui, expects most kids will be able to get vaccinated by the middle of next year.” writes Yahoo news.

The final word is that of Dr. Michael Yeadon, who holds a degree in Biochemistry & Toxicology & a research-based PhD in pharmacology. Dr. Yeadon spent 32 years working in pharmaceutical R&D and was a VP at Pfizer. He posted this letter to Twitter,

Whatever one’s views are about political management of the pandemic in [the] U.K., we believe strongly that mandated or coerced use in the wider population of part-developed vaccines should play no role whatsoever in recovering from it. 

Those at distinctly elevated risk of severe illness & death, of course should be offered it, using fully informed consent. But absolutely not mandated or coerced vaccination. We so argue this, because it’s illegal and unethical. It might be countered that this letter is superfluous because no one is suggesting it. Sadly, that isn’t true. On the contrary, senior figures from governments across the world are proposing exactly this. Leading U.K. politicians have worryingly even said that “our national policy now is to suppress the virus as much as possible until a vaccine becomes available.

Despite any promises of a non-coercive Covid shot, the government’s apparatus for ramming through all sorts of legislation to eliminate any barrier hindering injectable pharmaceutical product lines making their way into your body is well-established over the last few years. Starting with a measles outbreak in 2019, nearly 200 bills suddenly appeared, as if waiting for the right moment. It was clear it wasn’t about measles then, and perhaps in a short time, we may discover there may be more to this new vaccine push than simply attempting to stop a cold virus or save lives – a primary endpoint that the Covid trials weren’t even designed for in the first place.

 

Connect with Jefferey Jaxen at The HighWire




COVID 19: Mounting Evidence of International Fraud

COVID 19: Mounting Evidence of International Fraud

by Iain Davis, In This Together
November 16, 2020

 

COVID 19, and the subsequent governmental responses, appear to be part of an international conspiracy to commit fraud. It seems there is no evidence that a virus called SARS-CoV-2 causes a disease called COVID 19.

Sometimes you have to go with your gut. I am not an expert in genetics and, as ever, stand to be corrected. However my attention was drawn to some research published by the Spanish medical journal D-Salud-Discovery.  Their advisory board of eminently qualified physicians and scientists lends further credibility to their research. Their claim is astounding.

The genetic primers and probes used in RT-PCR tests to identify SARS-CoV-2 do not target anything specific. I followed the search techniques outlined in this English translation of their report and can corroborate the accuracy of their claims about the nucleotide sequences listed in the World Health Organisations protocols. You can do the same.

D-Salud-Discovery state there are no tests capable of identifying SARS-CoV-2. Consequently all claims about the alleged impact of COVID 19 on population health are groundless.

The entire official COVID 19 narrative is a deception. Ostensibly, there is no scientific foundation for any part of it.

If these claims are accurate we can state that there is no evidence of a pandemic, merely the illusion of one. We have suffered incalculable loss for no evident reason, other than the ambitions of unscrupulous despots who wish to transform the global economy and our society to suit their purposes.

In doing so this “parasite class” have potentially committed countless crimes. These crimes can and should be investigated and prosecuted in a court of law.

Identification of What Exactly?

The World Health Organisation (WHO) classified COVID-19 (COronaVIrus Disease 2019). They declared a global COVID 19 pandemic on March 11th 2020.

The WHO’s Laboratory testing guidance states:

“The etiologic agent [causation for the disease] responsible for the cluster of pneumonia cases in Wuhan has been identified as a novel betacoronavirus, (in the same family as SARS-CoV and MERS-CoV) via next generation sequencing (NGS) from cultured virus or directly from samples received from several pneumonia patients.”

The WHO’s claim is that the SARS-CoV-2 virus causes the disease COVID-19. They also allege this virus has been clearly identified by researchers in Wuhan.

In the WHO’s Novel Coronavirus 2019-nCov Situation Report 1, they state:

“The Chinese authorities identified a new type of coronavirus, which was isolated on 7 January 2020……On 12 January 2020, China shared the genetic sequence of the novel coronavirus for countries to use in developing specific diagnostic kits.”

These two statements from the WHO clearly suggest the SARS-CoV-2 virus was isolated (meaning purified for study) and then genetic sequences were identified from the isolated sample. From this, diagnostic kits were developed and distributed globally to test for the virus in towns, cities and communities around the world. According to the WHO and Chinese researchers, these tests will find the virus that causes COVID 19.

Yet the WHO also state:

“Working directly from sequence information, the team developed a series of genetic amplification (PCR) assays used by laboratories.”

The Wuhan scientists developed their genetic amplification assays from “sequence information” because there was no isolated, purified sample of the so called SARS-CoV-2 virus. They also showed electron microscope images of the newly discovered virions (the spiky protein ball containing the viral RNA.)

However, such protein structures are not unique. They look just like other round vesicles, such as endocytic vesicles and exosomes.

Virologists claim that it is not possible to “isolate” a virus because they only replicate inside host cells. They add that Koch’s postulates do not apply because they relate to bacteria (which are living organisms). Instead, virologists observe the virus’ cytopathogenic effects (CPE), causing cell mutation and degradation, in cell cultures.

When Chinese researchers first sequenced the full SARS-CoV-2 genome they observed CPE in Vero E6 and Huh7 cells. Vero E6 are an immortalised monkey cell line and Huh7 are immortalised cancer (tumorigenic) cells. Meaning they have been maintained in vitro (in petri dish cultures) for many years.

Central to the official SARS-CoV-2 story is the idea that it is a zoonotic virus, capable of bridging the species gap from animals to humans. When scientists from the U.S. CDC “infected” various cells with the novel virus they noted the following:

“We examined the capacity of SARS-CoV-2 to infect and replicate in several common primate and human cell lines, including human adenocarcinoma cells (A549) [lung celles], human liver cells (HUH7.0), and human embryonic kidney cells (HEK-293T), in addition to Vero E6 and Vero CCL81 [monkey cells]……No cytopathic effect was observed in any of the cell lines except in Vero cells [monkey cells]…….HUH7.0 and 293T cells showed only modest viral replication and A549 cells [human lung tissue cells] were incompatible with SARS-CoV-2 infection.”

The CDC did not observe any CPE in human cells. They saw no evidence that this alleged virus caused any human illness. Nor did this supposed human virus show any notable replication in human cells, suggesting human to human infection would be impossible.

Noting this problem, a team of Polish scientists introduced this sequenced “virus” to human epithethelium (airway) cells. They observed the effects on these HAE cultures for 5 days. They noted much greater replication than the CDC scientists but ultimately stated:

“We did not observe any release of the virus from the basolateral side of the HAE culture.”

Meaning they did not see any evidence of the supposed virions breaching the cell wall membrane. Again suggesting this so called virus isn’t infectious in human beings.

It is not clear that SARS-CoV-2 is a human virus capable of causing illness. It may not even physically exist. Is it nothing more than a concept based upon predictive genetic sequences?

Voyage Of Discovery

The Wuhan Center for Disease Control and Prevention and the Shanghai Public Health Clinical Centre published the first full SARS-CoV-2 genome (MN908947.1 ). This has been updated many times. However, MN908947.1 was the first genetic sequence describing the alleged COVID 19 etiologic agent (SARS-CoV-2).

All subsequent claims, tests, treatments, statistics, vaccine development and resultant policies are based upon this sequence. If the tests for this novel virus don’t identify anything capable of causing illness in human beings, the whole COVID 19 narrative is nothing but a charade.

The WUHAN researchers stated that they had effectively pieced the SARS-CoV-2 genetic sequence together by matching fragments found in samples with other, previously discovered, genetic sequences. From the gathered material they found an 87.1% match with SARS coronavirus (SARS-Cov). They used de novo assembly and targeted PCR and found 29,891-base-pair which shared a 79.6% sequence match to SARS-CoV.

They had to use de novo assembly because they had no priori knowledge of the correct sequence or order of those fragments. Quite simply, the WHO’s statement that Chinese researchers isolated the virus on the 7th January is false.

The Wuhan team used 40 rounds of RT-qPCR amplification to match fragments of cDNA (complimentary DNA constructed from sampled RNA fragments) with the published SARS coronavirus genome (SARS-CoV). Unfortunately it isn’t clear how accurate the original SARS-CoV genome is either.

In 2003 a team of researchers from from Hong Kong studied 50 patients with severe acute respiratory syndrome (SARS). They took samples from 2 of these patients and developed a culture in fetal monkey liver cells.

They created 30 clones of the genetic material they found. Unable to find evidence of any other known virus, in just one of these cloned samples they found genetic sequences of “unkown origin.”

CHART: E Gene target sequence

Examining these unknown RNA sequences they found 57% match to bovine coronavirus and murine hepatitis virus and deduced it was of the family Coronaviridae. Considering these sequences to suggest a newly discovered SARS-CoV virus (new discoveries being ambrosia for scientists), they designed RT-PCR primers to test for this novel virus. The researchers stated:

“Primers for detecting the new virus were designed for RT-PCR detection of this human pneumonia-associated coronavirus genome in clinical samples. Of the 44 nasopharyngeal samples available from the 50 SARS patients, 22 had evidence of human pneumonia-associated coronavirus RNA.”

Half of the tested patients, who all had the same symptoms, tested positive for this new alleged virus. No one knows why the other half tested negative for this novel SARS-CoV virus. The question wasn’t asked.

This supposed virus had just a 57% sequence match to allegedly known coronavirus. The other 43% was just “there.” Sequenced data was produced and recorded as a new genome as GenBank Accession No. AY274119.

The Wuhan researchers subsequently found an 79.6% sequence match to AY274119 and therefore called it a novel strain of SARS-CoV (2019-nCoV – eventually renamed SARS-CoV-2). No one, at any stage of this process, had produced any isolated, purified sample of any virus. All they had were percentage sequence matches to other percentage sequence matches.

Isolate Nothing

Scientists are very annoyed because they keep saying the virus has been isolated but no one believes them. This is because, as yet, no one has provided a single purified sample of the SARS-CoV-2 virus. What we have instead is a completed genome and, as we are about to discover, it isn’t particularly convincing.

Investigative journalists Torsten Engelbrecht and Konstantin Demeter asked some of the scientists who said they had images of SARS-C0V-2 virions to confirm these were images of an isolated, purified, virus. None of them could.

In Australia scientists from the Doherty Institute, announced that they had isolated the SARS-CoV-2 virus. When asked to clarify the scientists said:

“We have short (RNA) sequences from the diagnostic test that can be used in the diagnostic tests”

This explains why the Australian government state:

“The reliability of COVID-19 tests is uncertain due to the limited evidence base…There is limited evidence available to assess the accuracy and clinical utility of available COVID-19 tests.”

In The UK, in July, a group of concerned academics wrote a letter to the UK Prime Minister Boris Johnson in which they asked him to:

“Produce independently peer reviewed scientific evidence proving that the Covid-19 virus has been isolated.”

To date they have not received a reply.

Similarly, UK researcher Andrew Johnson made a Freedom of Information Request to Public Health England (PHE). He asked them to provide him with their records describing the isolation of a SARS-COV-2 virus. To which they responded:

“PHE can confirm it does not hold information in the way suggested by your request.”

Canadian researcher Christine Massey made a similar freedom of information request, asking the Canadian government the same. To which the Canadian government replied:

“Having completed a thorough search, we regret to inform you that we were unable to locate any records responsive to your request.”

In the U.S. the Centre For Disease Control (CDC) RT-PCR Diagnostic Panel state:

“…No quantified virus isolates of the 2019-nCoV are currently available……..Detection of viral RNA may not indicate the presence of infectious virus or that 2019-nCoV is the causative agent for clinical symptoms.”

Last updated on 13th July 2020, the CDC are yet to obtain any pure viral sample from any patient said to have the disease of COVID-19. They openly admit their tests don’t necessarily show if SARS-CoV-2 is either present or causes COVID 19.

We are told that none of this matters. That we are ignorant and just don’t understand virology. Therefore, we must except pictures of things we know could be something else and genetic sequences (which could be anything else) as conclusive proof that this virus, and the disease it is supposed to cause, are real.


Testing For Nothing

The WHO, and every government, think tank, policy steering committee, government scientific advisor, supranational institutions and others who promote the official COVID 19 narrative, assert that SARS-CoV-2 causes COVID 19. While no one has ever produced a sample of this supposed virus, the alleged SARS-CoV-2 genome has been published. It is in the public domain.

Key genetic sequences, in the SARS-CoV-2 genome, are said to have specific functions. These are the target proteins that scientists test for to identify the presence of the “virus”. These include:

  • RNA-polymerase (Rd-Rp) gene – This enables the SARS-CoV-2 RNA to replicate inside the cytoplasm of COVID 19 diseased epithelial cells.
  • S gene (Orf2) – this glycoprotein forms the spike on the SARS-CoV-2 virion surface which supposedly facilitates SARS-CoV-2 binding to the ACE2 receptors on cells, allowing the RNA inside the virion protein shell (capsid) to pass into the now infected cell.
  • E gene (Orf1ab) – small membrane protein used in viral assembly
  • N gene (Orf9a) – the nucleocapsid gene which binds the RNA in capsid formation

The WHO maintain a publicly available record of the RT-PCR primers and probes used to test for SARS-CoV-2. The primers are specific nucleotide sequences that bind (anneal) to the antisense and sense strands of the synthesised cDNA (called forward and reverse primers respectively.)

The cDNA strands separate when heated and reform when cooled. Prior to cooling, nucleotide sequences called probes are introduced to anneal to specific target regions of the suspected viral genome. During amplification, as the regions between primers elongate, when a primer strikes a probe, the probe decays releasing a fluorescent or dye which can then be read by researchers.

It is the identification of these markers which scientists claim to prove the presence of SARS-CoV-2 in a sample.

Something else which is publicly available is the Basic Local Alignment Search Tool (BLAST). This allows anyone to compare published nucleotide sequences with all those stored by the U.S. National Institutes of Health (NIH) genetic database called GenBank. Therefore we can BLAST the claimed SARS-CoV-2 primers, probes and target gene sequences.

The WHO’s forward, reverse primers and probe protocols, for the alleged SARS-CoV-2 viral genome, are based upon RdRp, Orf1, N and E gene profiles. Anyone can run them through BLAST to see what we find.

The vital RdRP nucleotide sequence, used as a forward primer is – ATGAGCTTAGTCCTGTTG. If we run a nucleotide BLAST this is recorded as a complete SARS-CoV-2 isolate with a 100% matched sequence identity. Similarly the reverse E gene primer sequence – ATATTGCAGCAGTACGCACACA – reveals the presence of the Orf1ab sequence which also identifies SARS-CoV-2.

However, BLAST also enables us to search the nucleotide sequences of the microbial and human genomes. If we search for the RdRp SARS-CoV-2 sequence it reveals 99 human chromosome with a 100% sequence identity match. The Orf1ab (E gene) returns 90 with a 100% sequence identity match to human chromosomes.

Doing the same for these sequences with a microbial search finds 92 microbes with a 100% match to the SARS-CoV-2 E gene and 100 matched microbes, with a 100% sequence identity, to the vital SARS-CoV-2 RdRp gene.

Whenever we check the so called unique genetic markers for SARS-CoV-2, recorded in the WHO protocols, we find complete or high percentage matches with various fragments of the human genome. This suggests that the genetic sequences, which are supposed to identify SARS-CoV-2, are not unique. They could be anything from microbial sequences to fragments of human chromosomes.

So called fact checkers, like Reuters’ Health Feedback project, have been quick to dismiss the claims of those who have noticed the apparent lack of specificity in the supposed SARS-CoV-2 genome. Using a slew of strawman arguments like, “this claim suggests every test should be positive,” (which it doesn’t) their debunking attempt runs something like this:

Primers are designed to bind to specific nucleotide sequences that are unique to the virus. The forward primer may bind to a particular chromosome but the reverse primer doesn’t bind to the same chromosome and so the chromosome is not present in the SARS-CoV-2 virus. Moreover because the forward and perverse primers envelop the sequence to be amplified the cDMA sequence between primers is unique to the virus.

This seems to deliberately misrepresent the significance of these findings by forwarding an argument that no one, other than the fact checkers themselves, are making. BLAST searches show that these target sequences are not unique to SARS-CoV-2. Nor do all targets need to be found for a result to be deemed positive.

Moroccan researchers investigated the epidemiology of Moroccan alleged cases of SARS-CoV-2. Nine percent were positive for three genes, eighteen percent were positive for two genes and seventy three percent for just one. As we have just discussed, many may have been positive for none.

This is entirely in keeping with WHO’s test guidelines. They state:

“An optimal diagnosis consists of a NAAT [nucleic acid amplification test] with at least two genome-independent targets of the SARS-CoV-2; however, in areas where transmission is widespread, a simple single-target algorithm can be used……One or more negative results do not necessarily rule out the SARS-CoV-2 infection.”

Regardless of the spurious arguments of well funded fact checkers, if the forward and reverse primers identify junk, perhaps one being the fragment of a chromosome and the other a microbial sequence, then the amplified region between them is probably junk too.

The argument that RT-PCR only finds RNA is specious. Natural transcription (the separation of DNA strands) occurs during gene expression. No one is saying whole chromosomes or microbes are sequenced in the alleged SARS-CoV-2 genome. Though they may, for all we know. They are saying the alleged markers, used to test for this supposed virus, are not fit for purpose.

RT-PCR tests do not sequence the entire genome. They look for incidents of specific probe florescence to indicate the presence of sequences said to exist. These sequences are defined by MN908947.1 and the subsequent updates. These primers and probes could reveal nothing but RNA matches extracted from non-coding, sometimes called “junk,” DNA (cDNA.)

For example the SARS-CoV-2 S gene is meant to be highly specific to the SARS-CoV-2 virus genome. The target sequence is – TTGGCAAAATTCAAGACTCACTTTC. A microbial BLAST search returns 97 microbial matches with 100% identity sequence match. The lowest identity percentage match, within the top 100, is 95%. A human genome BLAST also finds a 100% sequence match to 86 human chromosome fragments.

No matter where you look in the supposed genome of SARS-CoV-2, there is nothing in the WHO’s test protocols that clearly identifies what it is. The whole genome could be false. The tests do not prove the existence of SARS-CoV-2. All they reveal is a soup of unspecified genetic material.

If so, as there are no isolates or purified samples of the virus, without a viable test, there is no evidence that SARS-CoV-2 exists. Therefore, nor is there any evidence that a disease called COVID 19 exists.

This infers that there is no scientific basis for any claims about COVID 19 case numbers, hospital admissions or mortality figures. All measures taken to combat this deadly virus are quite possibly founded upon nothing.

Conclusive Fraud

Fraud is a criminal act. The legal definition of fraud is:

“Some deceitful practice or willful device, resorted to with intent to deprive another of his right, or in some manner to do him an injury.”

The Legal definition of a conspiracy is:

“A combination or confederacy between two or more persons formed for the purpose of committing, by their joint efforts, some unlawful or criminal act”

It seems, those who claim we face a pandemic have not provided any evidence to show that a virus called SARS-CoV-2 causes a disease called COVID 19. All of the information strongly suggesting this possibility is readily available in the public domain. Anyone can read it.

For there to be a fraud the deceit must be wilful. The intention must be to deliberately deprive others of their rights or injure them in some other way. If there is evidence of collusion between individuals ad/or organisations to commit fraud, then this is a conspiracy (in Common Law jurisdictions) or a Joint Criminal Enterprise (JCE) under International Law.

It seems COVID 19 has been deliberately used as a casus belli to wage war on humanity. We have been imprisoned in our own homes, our freedom to roam restricted, freedom of speech and expression eroded, rights to protest curtailed, separated from loved ones, our businesses destroyed, psychologically bombarded, muzzled and terrorised.

Worse still, while there is no evidence of unprecedented all cause mortality, there were unseasonable spikes in deaths. These correlate precisely with Lockdown measures which saw the withdrawal of the health services we pay for and a reorientation of public health services to treat one alleged disease at the exclusion of all others.

Further, it is proposed by those who have forwarded the COVID 19 story, that this alleged disease provides justification for the complete restructuring of the global economy, our political systems, societies, cultures and humanity itself.

To be allowed to participate in their so called “new normal,” which is the wholesale transformation of our entire society without our consent, they insist we submit to their conditions.

These include, but aren’t limited to, bio-metric surveillance of everyone, the centralised control and monitoring of all of our transactions, oppressive business and social restrictions and an effective demand that we have no right to sovereignty over our own bodies. This constitutes the condition of slavery.

There is no doubt that we have been deprived of our rights and injured. In Common Law jurisdictions innocence is presumed, but the evidence that harm has been deliberately caused by an international conspiracy is overwhelming. Destructive policies, enacted by governments across the world, clearly originated among globalist think tanks and supranational institutions long before the emergence of this non existent pandemic.

In Napoleonic Code jurisdictions, guilt is presumed. In order for the accused conspirators to prove their innocent they must show that, despite their immeasurable resources, they have collectively been unable to access or understand any of the freely available evidence suggesting COVID 19 is a myth.

Those responsible for the crime of conspiracy to commit global fraud should be tried. If found guilty they should be imprisoned while the rest of us get on with trying to repair the damage they have already inflicted.



Author Iain Davis is an independent researcher and short filmmaker and the author of the new book, A Dangerous Ideology. See more of Iain’s work at his blog site In This Together and follow him at Twitter & Steemit & MINDS

 

Connect with Iain Davis at In This Together

 

 




David Icke: New Definition of Insanity — Having the Gates Vaccine

New Definition of Insanity: Having the Gates Vaccine

by David Icke
November 20, 2020

 



Video available at David Icke BitChute channel.

[As a service to protect truth from censorship & to share widely, mirrored copies of this video are available at Truth Comes to Light BitChute, Brighteon, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]

 

cover image credit pixunfertig / pixabay

 




COVID-19 vs Homo Sapiens Ascorbicus

COVID-19 vs Homo Sapiens Ascorbicus

by Theo Farmer, Orthomolecular.org
November 20, 2020

 

(OMNS Nov 20, 2020) On an orthomolecular farm, one that uses no agricultural chemicals, and no pharmaceutical products with animals or farmers, we have a different perspective on viruses, and thus our response to the COVID19 situation may be counter to what is generally propagating in the mainstream.

For those who are unfamiliar with this topic, just a warning. This might be uncomfortable to read, but healing is not necessarily comfortable. It would be good to start with some history.

Vitamin C Mutants

In 1979, Irwin Stone published a paper, a medical hypothesis, entitled Homo Sapiens Ascorbicus, a Biochemically Corrected Robust Human Mutant. [1] Stone had been researching vitamin C and publishing papers on it for decades, and personally was taking lots of vitamin C in an attempt to match the levels he knew that animals make in their bodies continuously.

He and his wife had been in a head-on collision years earlier where he had broken most of his bones. Both had been taking many grams of vitamin C daily, and, to the surprise of medics that arrived on the scene, neither were in shock when the ambulance arrived. He was told that he would never walk again, but he was fully recovered and walking in 3 months, and he attributed that to his taking 50-60 grams of vitamin C a day while in the hospital. Stone and his wife had both experienced being the robust human mutants that he described in his paper.

What Irwin Stone knew was that a goat our size, when under stress, can produce up to 100 grams per day of vitamin C, converting glucose, blood sugar, to ascorbate. [2] Humans produce none, but we have the same mammalian cells as a goat and the same need for ascorbate, according to Stone. Stone called ascorbate “the healing factor” and he and other vitamin C researchers felt that calling ascorbate a “vitamin” did not adequately describe its necessity in helping humans prevent and heal from disease and injury.

Orthomolecular vs Pharma

Double Nobel Laureate, Linus Pauling, coined the term “orthomolecular” in 1968 in an article he published in the journal Science which was titled “Orthomolecular Psychiatry.” [3] In 1970, he wrote the bestselling book Vitamin C and the Common Cold. [4] In it is a chapter where he criticizes the pharmaceutical industry of the time for selling toxic chemicals as cold remedies when all humanity needed to know was to take high levels of ascorbate to neutralize viral infections.

Also in the 1970s, Pauling’s colleague at Stanford, Dr. Robert Cathcart treated thousands of people for various diseases in his private practice using only oral ascorbic acid. His research showed us that any viral infection could be addressed by raising the ascorbate level in the body high enough. [5] So viruses, even viral pneumonia, handled by people who are “skilled at taking vitamin C” as Cathcart put it, were a non-issue. Essentially Cathcart showed that, to the robust human mutant called Homo Sapiens Ascorbicus, viruses are a non-issue. [6]

Also by the 1970’s, the pharmaceutical industry apparently had been granted controlling influence by the mass media and governments of the world, and had a huge influence on the information distributed through our educational systems. They had essentially programmed humanity into building a dependency on their industry and products. They took control of both sides of every argument, arguing that vitamin C was important for every human, and that everyone needed to take vitamin C daily only in MILLIGRAM quantities, and they propagated rumors about the dangers of overdosing vitamin C. Mainstream medicine marginalized the information that Pauling was trying to get out, shoved his message off into a hidden corner, and those of us who grew up in the 60’s and 70’s simply weren’t trained to understand vitamin C and our human need for vitamin C. Today, the mainstream is still trapped in a model that was essentially obsoleted by Pauling and his orthomolecular colleagues in the 1970s. This industrial medicine model leads us astray from optimal health for ourselves and our children, even though it claims to offer “advanced” solutions.

Fortunately, Pauling’s Orthomolecular medicine continued to develop over the decades, in the background, and it continues to evolve today, healing people using only proper doses of nutrients. [7,8] Today, orthomolecular medicine, with only nutrients in its tool chest, is a serious competitor to the dominant pharmaceutical medicine model. Many of orthomolecular treatments are effective at relieving disease in a few hours or even a few minutes, as in the case of using vitamin C in a nebulizer for lung issues like asthma. [9] And it’s very easy for any human to prove that taking a few grams of vitamin C every 15 or 30 minutes during a day can shut down a virus, any virus, even a “novel” virus. [10,11]

Orthomolecular Farming

Somewhat battered by the dominant “health care” paradigm, my wife, Kira, and I started livestock farming with a commitment to living in a new paradigm: being pharmaceutical free and chemical free in all of our living and farming methods. We had knowledge and experience using vitamin C when we started this 160-acre farm. We had already used it for things like shutting down viral pneumonia and eliminating Kira’s dependency on epi-pens when she got stung by a wasp, and we used it to help a horse heal a broken hip bone. I had personally shut down many colds and other viruses in a day or two and was discovering how I could prevent sunburn and other radiation damage using Vitamin C and E [12, 13]. We kept my handicapped son Cameron going for years beyond his life expectancy by high dosing him with vitamin C when he had respiratory issues. We already had one grandchild, Helios, who was a vitamin C baby, and since then, we’ve welcomed more vitamin C baby grandchildren.

Each of these cascading experiences are powerful revelations on our journey to a new paradigm based on truth. Through our personal experiences, and by contrasting our gullibility earlier in life with the dramatic health benefits we realized and observed by high dosing vitamin C, we are becoming . . .

A New Farmer Species

One cause of “circling disease” in cattle is listeriosis, an infection that inflames the covering of the cow brain, similar to meningitis in humans. [14] In the mainstream veterinary model, this is a fatal disease in cows. A circling cow is about to die without massive antibiotic treatment, and even with that expensive treatment, it’s most likely to die. But with an understanding of the biochemistry of ascorbate in animals, this is a simple disease to treat, completely resolvable within hours. [15].

As orthomolecular practitioners with extensive experience dealing with all kinds of animal and human health issues using only high dose nutrients, we are simply not impressed by the mainstream COVID19 misinformation. Since we started this farm, we have been telling people that we are immersed in misinformation: lies about raw milk being dangerous, lies about food additives being safe, lies and obfuscation about nutrients, lies about vaccines being safe and useful, and, by omission, about the importance and power of a balanced microbiome in the soil, plants, animals, and humans.

When you have proven for yourself the truth, the lies have no traction. We have become, in essence, immune to the lies.

Mask-free, Gloves-free, Disinfectant-free

I titled this article “COVID19 vs Homo Sapiens Ascorbicus” because I think one of the main things we’ve proven in the years on this farm, and continue to prove daily, is Irwin Stone’s hypothesis. On this farm, we strive to match the levels of vitamin C in our bodies that animals produce. In doing so, we have become the robust human mutants that Irwin Stone predicted was possible all the way back in 1979. The reason we don’t worry about viruses, even novel viruses, is because they don’t affect the animals here and they don’t affect the homo sapiens ascorbicus farmers that we have become.

To the robust mutant, I have to say that the world has looked very strange for a long time, way before the COVID19 craze.

Out in the world, back when we were “original-recipe” homo sapiens, we were ignorantly downing food additives like polysorbate-80 (an emulsifier) in processed foods assuming it was safe, when in actuality it was damaging our gut microbiome, and we were injecting the same additive in vaccines to “boost the immunity of our children,” when in actuality it was opening up their blood brain barriers to the flow of more toxins.

Now, as transformed mutants, we no longer buy into the logic behind these practices. Homo sapiens ascorbicus aren’t affected by, and certainly don’t fear, viruses. So using pharmaceutical products to treat disease or alter our immune systems or the immune systems of our animals doesn’t make any sense.

As homo sapiens ascorbicus, we choose not to comply with unconstitutional dictates like masks, gloves, and Purell to avoid a disease that will never affect us. To our subspecies, those dictates look positively tyrannical. We know how to prevent viral infection using vitamin C, and, fortunately, we also know that high dosing vitamin C will protect us from the carcinogenic “sanitation” products being sprayed and spread freely now from shopping cart to shopping cart, on plexiglass and pin pads, and airborne in the stores that we must frequent in our quest to recruit and transform new homo sapiens ascorbicus. If you happen to see a maskless farmer in the crowd, you may be looking at one of the new, robust homo sapiens ascorbicus “mutants” that Irwin Stone predicted back in 1979. We are that new orthomolecular “species.”

A New Model

One of the founding quotes of our farm is from Buckminster Fuller, who was a brilliant contemporary of Linus Pauling. Fuller said, “You never change things by fighting against the existing reality. To change something, build a new model that makes the old model obsolete.”

For the last decade, we have been busy building a new reality, a farm community that homo-sapiens ascorbicus prefer to live in, one that better fits our robust mutant transformation. In observing the happenings of 2020, it seems that the existing reality, which is currently dominated by homo sapiens (original version), is failing and fading away into fear and overdue obsolescence. The new model is ours for the building, and the new model will be occupied by fearless mutants of the species homo sapiens ascorbicus and many others who, in their own way, have transcended the hysteria of the mainstream narrative.

So that’s an orthomolecular farmer’s response to COVID19. If you haven’t already figured out your relationship to ascorbic acid, ascorbate, the healing factor, vitamin C, you might want to. It will change your life. However, be aware that you may become a robust human mutant as well and you may find yourself with a naked face in a crowd of masked homo-sapiens who live in an obsolete reality.

(Theo Farmer administers the Facebook and MeWe groups titled “Vitamin C and Animals.” He is also the author of the children’s book Buttercup, Me and Vitamin C, a free pdf download at https://www.hfpma.online/shop )

Editor’s note: The views expressed in this article are the author’s and not necessarily that of all members of the Orthomolecular Medicine News Service Editorial Review Board. OMNS welcomes divergent opinions and discussion on a variety of subjects. Readers may submit their own article drafts to the Editor at the contact email below.

References

1. Stone, I. (1979) Homo Sapiens Ascorbicus, A Biochemically Corrected Robust Human Mutant. Med Hypotheses, 5:711-721. https://pubmed.ncbi.nlm.nih.gov/491997

2. Chatterjee IB, Majumder AK, Nandi BK, Subramanian N. (1975) Synthesis And Some Major Functions Of Vitamin C In Animals. Annals of the New York Academy of Sciences 258 Second Confer: 24-47. https://nyaspubs.onlinelibrary.wiley.com/doi/epdf/10.1111/j.1749-6632.1975.tb29266.x

3. Pauling L. (1968) Orthomolecular psychiatry. Varying the concentrations of substances normally present in the human body may control mental disease. Science. 160:265-271. https://pubmed.ncbi.nlm.nih.gov/5641253

4. Pauling L. (1970) Vitamin C and the Common Cold. W.H.Freeman & Co. ISBN-13:978-0425048535

5. Cathcart RF (1981) Vitamin C, titrating to bowel tolerance, anascorbemia, and acute induced scurvy. Med Hypotheses, 7:1359-1376. http://doctoryourself.com/titration.html

6. Cathcart RF. Vitamin C pioneer. https://www.youtube.com/watch?v=VkkWDDSti_s

7. Journal of Orthomolecular Medicine. http://orthomolecular.org/library/jom

8. Orthomolecular Medicine News Service. http://orthomolecular.org/resources/omns

9. Levy T. (2019) Reboot Your Gut: Optimizing Health and Preventing Infectious Disease. Orthomolecular Medicine News Service. http://www.orthomolecular.org/resources/omns/v15n16.shtml

10. Hickey S, Roberts H, Downing D. (2014) Can Vitamin C Cure Ebola? Orthomolecular Medicine News Service. http://orthomolecular.org/resources/omns/v10n13.shtml

11. AscorbateWeb. An historical compendium of 20th-Century medical & scientific literature attesting to the efficacy of ascorbate (a.k.a. “Vitamin C”) in the treatment and prevention of human and animal illnesses and diseases. https://www.seanet.com/~alexs/ascorbate

12. OMNS (2012) Vitamin C Prevents Radiation Damage: Nutritional Medicine in Japan. Orthomolecular Medicine News Service. http://www.orthomolecular.org/resources/omns/v08n06.shtml

13. Hickey S, Yanagisawa A, Saul AW, Schuitemaker GE, Downing D. (2012) Fukushima Radiation Release is Worse than You Have Been Told: What You Can Do to Protect Yourself. Orthomolecular Medicine News Service http://orthomolecular.org/resources/omns/v08n17.shtml

14. The Cattle Site. listeriosis. https://www.thecattlesite.com/diseaseinfo/192/listeriosis

15. Farmer T. (2020) C is for Cattle: How high-dose ascorbate therapy works on the farm. Orthomolecular Medicine News Service. http://orthomolecular.org/resources/omns/v16n52.shtml

Nutritional Medicine is Orthomolecular Medicine

Orthomolecular medicine uses safe, effective nutritional therapy to fight illness. For more information: http://www.orthomolecular.org

Find a Doctor

To locate an orthomolecular physician near you: http://orthomolecular.org/resources/omns/v06n09.shtml

The peer-reviewed Orthomolecular Medicine News Service is a non-profit and non-commercial informational resource.

Editorial Review Board:

Seth Ayettey, M.B., Ch.B., Ph.D. (Ghana)
Ilyès Baghli, M.D. (Algeria)
Ian Brighthope, MBBS, FACNEM (Australia)
Gilbert Henri Crussol, D.M.D. (Spain)
Carolyn Dean, M.D., N.D. (USA)
Ian Dettman, Ph.D. (Australia)
Damien Downing, M.B.B.S., M.R.S.B. (United Kingdom)
Ron Erlich, B.D.S. (Australia)
Hugo Galindo, M.D. (Colombia)
Martin P. Gallagher, M.D., D.C. (USA)
Michael J. Gonzalez, N.M.D., D.Sc., Ph.D. (Puerto Rico)
William B. Grant, Ph.D. (USA)
Tonya S. Heyman, M.D. (USA)
Suzanne Humphries, M.D. (USA)
Ron Hunninghake, M.D. (USA)
Robert E. Jenkins, D.C. (USA)
Bo H. Jonsson, M.D., Ph.D. (Sweden)
Felix I. D. Konotey-Ahulu, MD, FRCP, DTMH (Ghana)
Jeffrey J. Kotulski, D.O. (USA)
Peter H. Lauda, M.D. (Austria)
Thomas Levy, M.D., J.D. (USA)
Alan Lien, Ph.D. (Taiwan)
Homer Lim, M.D. (Philippines)
Stuart Lindsey, Pharm.D. (USA)
Victor A. Marcial-Vega, M.D. (Puerto Rico)
Charles C. Mary, Jr., M.D. (USA)
Mignonne Mary, M.D. (USA)
Jun Matsuyama, M.D., Ph.D. (Japan)
Joseph Mercola, D.O. (USA)
Jorge R. Miranda-Massari, Pharm.D. (Puerto Rico)
Karin Munsterhjelm-Ahumada, M.D. (Finland)
Tahar Naili, M.D. (Algeria)
W. Todd Penberthy, Ph.D. (USA)
Selvam Rengasamy, MBBS, FRCOG (Malaysia)
Jeffrey A. Ruterbusch, D.O. (USA)
Gert E. Schuitemaker, Ph.D. (Netherlands)
T.E. Gabriel Stewart, M.B.B.CH. (Ireland)
Thomas L. Taxman, M.D. (USA)
Jagan Nathan Vamanan, M.D. (India)
Garry Vickar, M.D. (USA)
Ken Walker, M.D. (Canada)
Raymond Yuen, MBBS, MMed (Singapore)
Anne Zauderer, D.C. (USA)
Andrew W. Saul, Ph.D. (USA), Editor-In-Chief
Associate Editor: Robert G. Smith, Ph.D. (USA)
Editor, Japanese Edition: Atsuo Yanagisawa, M.D., Ph.D. (Japan)
Editor, Chinese Edition: Richard Cheng, M.D., Ph.D. (USA)
Editor, French Edition: Vladimir Arianoff, M.D. (Belgium)
Editor, Norwegian Edition: Dag Viljen Poleszynski, Ph.D. (Norway)
Editor, Arabic Edition: Moustafa Kamel, R.Ph, P.G.C.M (Egypt)
Editor, Korean Edition: Hyoungjoo Shin, M.D. (South Korea)
Assistant Editor: Helen Saul Case, M.S. (USA)
Technology Editor: Michael S. Stewart, B.Sc.C.S. (USA)
Legal Consultant: Jason M. Saul, JD (USA)

Comments and media contact: drsaul@doctoryourself.com OMNS welcomes but is unable to respond to individual reader emails. Reader comments become the property of OMNS and may or may not be used for publication.

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Truth Comes to Light editor’s note: I recommend the work of Dr. Andrew Kaufman and Dr. Tom Cowan to understand the research showing that viruses are not at all what we have been taught. ~ Kathleen

See related articles from this site:

Exposing the Lie — Hippocratic Hypocrisy: A Tale of Two Snakes

 

The Contagion Fairy Tale

 

The Deception of Virology & Vaccines | Why Coronavirus Is Not Contagious

Dr. Tom Cowan w/ Dr. Andrew Kaufman: Strong Intuition and Deep Research Are Exposing the Medical Lies Used to Instill Fear in Humanity




Dr. Andrew Kaufman: Reviewing the Recently Published Danish Study on Effectiveness of Masks

Dr. Andrew Kaufman: Reviewing the Recently Published Danish Study on Effectiveness of Masks

by Dr. Andrew Kaufman
November 19, 2020

 



Available at Dr. Andrew Kaufman’s LBRY or YouTube channels.

After being denied publication by three major journals, the Danish group has finally been published in the Annals of Internal Medicine. You won’t be surprised by what they found if you are part of this community. We now have some high quality evidence on our side. Check out the paper here:

“Effectiveness of Adding a Mask Recommendation to Other Public Health Measures to Prevent SARS-CoV-2 Infection in Danish Mask Wearers. A Randomized Controlled Trial”

Dr. Kaufman will be speaking at the World Freedom Alliance Rally in Copenhagen, Denmark on Saturday, November 21, 2020.

 

Connect with Dr. Andrew Kaufman at AndrewKaufmanMD.com

cover image credit AnnaliseArt / pixabay




Fourth Gardasil Lawsuit Against Merck Alleges Its HPV Vaccine Caused Debilitating Injuries

Fourth Gardasil Lawsuit Against Merck Alleges Its HPV Vaccine Caused Debilitating Injuries
“I want to warn kids of the terrible risks for this vaccine and let other injured girls know that they are not alone. The Gardasil vaccine stole my life. Before Gardasil, my future was filled with endless possibilities.”

by Robert F. Kennedy, Jr., Children’s Health Defense
November 18, 2020

 

Today, the national law firm of Baum Hedlund Aristei & Goldman and I filed our fourth Gardasil lawsuit against Merck, on behalf of Sahara Walker, 19, of Lake Mills, Wisconsin, who suffered debilitating injuries from the HPV vaccine.

When she took the Gardasil jab at age 11, Sahara was happy, healthy, popular, athletic and an academic superstar who had just scored in the top 97th percentile of all Wisconsin students in math.

Two days later, Sahara was vomiting and experiencing headaches, severe body aches, fevers and soul-crushing fatigue that made her sleep her days away. Within a month she was either bedridden or wheelchair bound.

Her symptoms worsened. In 2015, Sahara endured 54 doctor appointments and her medication regimen climbed to 55 pills per day. Specialists diagnosed Sahara with neurocardiogenic syncope, postural orthostatic tachycardia (POTS), a form of orthostatic intolerance called orthostatic hypotension, small fiber neuropathy and severe autoimmune autonomic neuropathy. Her injuries forced her to homeschool from grades 6 to 12.

Today, Sahara, 19, takes 14 prescription medications and receives an expensive intravenous immunoglobulin treatment every three weeks.

“I want to warn kids of the terrible risks for this vaccine and let other injured girls know that they are not alone,” Sahara explained. “The Gardasil vaccine stole my life. Before Gardasil, my future was filled with endless possibilities. Now, my life is a parade of accommodations and medical interventions. It’s not how a 19 year old should live. I’m fighting for all of us.”

If Merck had warned Sahara’s mother about Gardasil’s dangers, she never would have allowed her daughter to receive the HPV vaccine.

“We are pro-vaccine, but we would have never had Sahara get Gardasil if we knew the risks,” Sahara’s mother said. “She went from perfectly healthy to sick and disabled within days of the shot. It’s beyond any doubt that Gardasil caused her injuries.”

Internal documents showed that Merck cherry-picked its own data to mislead the U.S. Food and Drug Administration and doctors about Gardasil’s safety and efficacy. We aim to get justice for Sahara and others impacted and to force Merck to stop defrauding the public so that we can protect our children.




David Icke w/ Former FEMA Operative Celeste Solum: Barcoding You Via PCR Tests, Vaccines, Mass Depopulation, Terraforming & Transforming All Life on Earth

David Icke w/ Former FEMA Operative Celeste Solum: Barcoding You Via PCR Tests, Vaccines, Mass Depopulation, Terraforming & Transforming All Life on Earth

Video by David Icke.
Links and excerpts provided by Truth Comes to Light editor. 

 

Conversation excerpts:


Celeste Solum:

“My breaking news is, anyone, anyone who has taken a covid test — they have placed a magnetic beacon. You have been tagged. You have been barcoded. And I am going to provide you the evidence of that today…” 

“I also want to draw people’s attention to the word ‘illuminate’…I don’t know if you’ve recognized it, but as an organic farmer, I have. It’s like things looked like a different color. The colors were not the same as before. .. I tripped on, in my research, that these forces and powers that are retooling and restructuring our planet, have restructured light.”

David Icke:

“A lot of people are now seeing about changing humans and barcoding humans — changing the nature of humans — but they want to change the nature of all life on earth, no matter what it is…”

###

Celeste Solum:

“Right now, your doctor can get paid for your execution…”

David Icke:

It’s a difficulty that people have… to grasp just the scale of psychopathic, frikking evil that we’re dealing with.”

###

Celeste Solum:

You can imagine my horror when, in January, I went to the World Economic Forum and I saw all those plans and they had been operationalized. So, no longer were they on the shelf. No longer were they sitting in computers. All the public leaders around the world were declaring that they were operationalized, which means that they were activated…

This covid situation is the first deployment of a construct, a new lifeform, if you will  It is not a virus. It is a nano, synthetic, biological life…– and what I mean by that is they have learned how, through evil technology, to fuse biological life and robotics. And the purpose of that is for extermination — because they don’t want anything of the old world. They want a new world…

I can show you military documents that talk about the old humans and the new humans. And they want, by 2025, to have the old humans eradicated. And any human from now on basically has to be engineered in a laboratory and enhanced and augmented and part of the matrix…”

###

David Icke: 

“It makes perfect sense to me because, where I’m coming from… is that behind all this is a force that isn’t human. And it’s working through this network of, I think, largely hybrids — running this web that I call the global cult. And this non-human force is basically assimilating and transforming humans and human life — and, indeed, all life on earth, to fit its own design. And it’s been operating in the background. You can see it mentioned in all the ancient cultures, the Bible, everywhere… And it then makes sense that they would see us, as humans, in the way some humans see animals.”

Celeste Solum:

“Yeah. Basically, they believe that they are the custodians of the animals or the stock, the chattel. We’re nothing to them. And now is the time. They tolerated us for a time… But now is the time that they want to eradicate all life that is not made in a laboratory…”

###

David Icke: 

“…It seems, as I’ve observed their mentality through the years, that they are obsessed with order… They are very ill-at-ease with states of flux that they don’t control…”

###

Celeste Solum:

“They are retooling and rewiring our bodies. Each one of us right now has 20,000 to 30,000 nanoparticles… They’re not active… Right now, they are in a sensory capacity…”

David Icke:

“It’s clear — the whole agenda of transforming the human body. How is this going to be impacted by the covid vaccine? Because when you’ve got these psychopaths insistent, not least through mandatory, that every man, woman and child on the planet is vaccinated with this thing. It’s obviously not about a virus. It’s about the transformation of everyone’s body….” 

Celeste Solum:

“So many years ago, like over decades ago, DARPA wanted to put chips into…”

David Icke:

“For people who don’t know, DARPA is the technological development arm of the Pentagon and gives evil a bad name.”

Celeste Solum:

” Well, they do black ops…

So they wanted to put chips and RFIDs… in people’s brains but they didn’t want to have to do surgery. So after many, many years they came up with a gel that would do the same thing… This gel is called hydrogel or Quantum Dot…

So what will happen with the vaccine is, you’ll get it injected into you and then it assembles — it self assembles. And then it swarms through your body. There are 33 different classifications… of robots — each with a different mission and a payload deployed into your body…” 

###

David Icke:

“What’s the relevance to all of this… of the whole tecno-electromagnetic-5G web that’s being built all around us?… Does it have an effect of activating this to another level?”

Celeste Solum:

“So basically, how it works is they deployed all these…nano synbios into our body that… Their bellies are hollow. They can carry a poison… It can carry a virus, a bacteria, a fungus. It can carry… it has explosive capabilities — more explosive capability (one nanoparticle) than TNT… It gets its marching orders from the frequency that is being aimed at it. “

###

Celeste Solum:

“Back at the parting of the Red Sea in the Bible, it says the seas split. In the Hebrew… it talked about the sea coagulated like curds… And so, another breaking news story that I’m going to be sharing this week is —  between an enzyme and these nanoparticles they are coagulating our body like cheese curds. 

…what the doctor’s perceived as pneumonia was not pneumonia but a swarming of the nanoparticles into the lungs, making a… primitive coagulation– but they intend to do this to the whole bloodstream.  So, if they’re not going to get you one way, they’re going to get you another way.”

###

David Icke:

“What’s the significance then of … sticking this probe up people’s noses —  just fo this test — right up to the brain?”

Celeste Solum:

“A couple of different things. One, if you pierce the blood-brain barrier… But they really don’t need that because they’ve already figured out how to get this — these nanoparticles — to cross the blood-brain barrier. But you are then getting, in many instances, the hydrogel straight into the brain. It doesn’t even have to travel through the body…”

###

David Icke:

“The bottom line is, take your mind back. And stop just doing or believing what authority tells you…

Whatever happens, we keep going. Because not keeping going is just not an option.”

 

 

Original video is available at David Icke BitChute channel.

[As a service to protect truth from censorship & to share widely, mirrored copies of this video will be  available at Truth Comes to Light BitChute, Brighteon, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]

Links mentioned in this interview:


World Economic Forum: Pioneers of Change Summit 2020

International Barcode of Life

Consortium for the Barcode of Life

Barcode of Life Data Systems

Clade X Pandemic Exercise Segment 1, Segment 2, Segment 3, Segment 4

PhyloCode

CIA Declassified & Sanitized version of The Adam and Eve Story (PDF)

World Organisation for Animal Health

Terrestrial Animal Health Code     Terrestrial Animal Health Code PDF

Terrestrial Manual — Manual of Diagnostic Tests and Vaccines for Terrestrial Animals

Aquatic Animal Health Code

Definition of “Stamping Out”

Manual on Procedures for Disease Eradication by Stamping Out 

The Beacon® Optofluidic System

Bill Gates and MIT Unveil Quantum Dots to Mark Children

DNA-Conjugated Magnetic Nanoparticles for Bio-Analytical and Biomedical Applications 


Celeste has a paid website/channel/community at $25 per month here: https://celestialreport.com

Celeste’s Christian/blblical-focused (free) website is shepherdsheart.life

Free content for Celeste will be coming soon on YouTube. Previously her free content was shared at diamondisc channel but will be moving to a new channel.  Check back with diamondisc for details: https://www.youtube.com/user/diamondisc/videos

Connect with David Icke at DavidIcke.com & Ickonic.com

 


 See videos related to The Story of Adam and Eve unclassified CIA document:

The Next End of the World | C.I.A. Classified

Bizarre Secret Files Released on Lost Ancient Human Civilizations…

 




Portuguese Court Rules PCR Tests as Unreliable & Unlawful to Quarantine People

Portuguese Court Rules PCR Tests as Unreliable & Unlawful to Quarantine People

by GreatGameIndia
November 18, 2020

 

The court stated, the test’s reliability depends on the number of cycles used and the viral load present. Citing Jaafar et al. 2020, the court concludes that

“if someone is tested by PCR as positive when a threshold of 35 cycles or higher is used (as is the rule in most laboratories in Europe and the US), the probability that said person is infected is less than 3%, and the probability that said result is a false positive is 97%.”

The court further notes that the cycle threshold used for the PCR tests currently being made in Portugal is unknown.

The threshold cycles used in PCR tests in India is between 37 and 40, which makes the reliability of the PCR test less than 3% and the false positive rate as high as 97%.

This case concerned the fact that four people had been quarantined by the Regional Health Authority. Of these, one had tested positive for COVID using a PCR test; the other three were deemed to have undergone a high risk of exposure. Consequently, the Regional Health Authority decided that all four were infectious and a health hazard, which required that they go into isolation.




Dr. Tom Cowan: The PCR Test is NOT a Valid Diagnostic Tool

The PCR Test is NOT a Valid Diagnostic Tool

by Dr. Tom Cowan
November 17, 2020

 



Original video is available at Dr. Tom Cowan YouTube channel.

[As a service to protect truth from censorship & to share widely, mirrored copies of this video are available at Truth Comes to Light BitChute, Brighteon, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]




ICAN’s Attorneys on Medical Exemptions to Masks

ICAN’s Attorneys on Medical Exemptions to Masks

by Informed Consent Action Network. ICanDecide.org
November 17, 2020

 

Del Bigtree asked ICAN’s attorneys to explain when someone can claim a medical exemption and whether a business can ask for proof of the medical exemption.

ICAN’s attorneys, led by Aaron Siri, provided this letter.  In short, ICAN has been advised that, upon asserting a medical exemption to wearing a mask, the business cannot ask for proof of the medical exemption.

If you want to complete a self-assessment to determine if you have a medical exemption to wearing a mask, here are self-assessment forms for residents in New YorkCalifornia, and Texas.  If you would like a self-assessment form for another state, please let us know!

 

Connect with Informed Consent Action Network, ICanDecide.org




Agendas & Doublespeak Mar Covid Vaccine’s Pending Release

By Jefferey Jaxen, The HighWire
November 16, 2020

 

With so little information public, and the information we do have is not genuinely encouraging, a cynical person might suggest the only thing breathless media coverage of Covid vaccine news has done is create pump-and-dump stock opportunities for investors.

As Bloomberg wrote: There’s ‘a wave of euphoria’ surging through global finance markets. Hooray? Pfizer’s latest stock surge was supported by press release hopium rooted in Science™. Like corporate media’s reporting on vaccine Science™, inconvenient truths are misrepresented, glossed over or outright ignored.

Just as Pfizer’s recent press release hyped its first interim analysis from its phase 3 study, the company’s CEO Albert Bourla sold 61% of his stock,  netting him a cool $5.6M.

The sale was part of a pre-scheduled 10b5-1 trading plan. So were Moderna’s Chief Medical Officer Tal Zaks and their CEO Stephan Bancel,  who made $63,069,210 and $58,591,783 respectively over the last six months with the world’s eyes on their vaccine development milestones. Optics be damned, as the companies simultaneously gobble up taxpayer money while their leadership unload stocks at record pace.

Science™ by press releases get dissected almost immediately nowadays, laying bare their shortcomings. Covid vaccine makers and their front men are throwing out big numbers to grab headlines across corporate media. Operation Warp Speed head contractor Dr. Moncef Slaoui said Friday, speaking from the White House Rose Garden (through a mask), that 20 million Americans could receive the shot by December. Followed up with 25-30 million each month after that.

Two narratives are running parallel throughout media to direct two different types of consumers. While the ‘pump and dump’ headlines target investors, the ‘vaccine will save us all’ reporting aims at the eventual mandatory consumers.

Sometimes the two meet in the middle and the veil lifts. For instance,  Reuters recent articleEurope ‘must grit teeth’ on COVID-19 as vaccine euphoria fades

Reading between the lines, Reuters might be telling investors to be on the lookout for the next Science™ by press release before making any financial moves, while commoners in Europe under second lockdown, “must grit [your] teeth.” Or perhaps another translation: Don’t mistake our media hype aimed at investors to think you’ll get out of your [second] unscientific lockdown anytime soon, Europe!

Similarly, Yahoo News ran the headlinePfizer vaccine could be key to conquering COVID-19 — but don’t throw away your mask yet. One statement message for investors, another for people under authoritarian edicts.

A recent BMJ analysis by Peter Doshi reviewed Covid vaccine frontrunners. Current trials, hyped at every turn, aren’t designed to save lives. Doshi writes, “None of the trials currently underway are designed to detect a reduction in any serious outcome such as hospital admissions, use of intensive care, or deaths. Nor are the vaccines being studied to determine whether they can interrupt transmission of the virus.

He continues, “In all the ongoing phase III trials for which details have been released, laboratory confirmed infections even with only mild symptoms qualify as meeting the primary endpoint definition. In Pfizer and Moderna’s trials, for example, people with only a cough and positive laboratory test would bring those trials one event closer to their completion.”

So why are we waiting for a vaccine to save us when its basic metrics aren’t designed to do so? In the early days of the coronavirus response, all measures were predicated on things going back to normal once the vaccine arrived. Now headlines have drastically changed. Lockdowns are here and increasing and your masks aren’t coming off when the vaccine savior arrives.

Yet that’s not stopping Ticketmaster or the airlines. Both are now considering digital vaccine verification to attend concerts or travel. A billboard.com exclusive reports, “After purchasing a ticket for a concert, fans would need to verify that they have already been vaccinated (which would provide approximately one year of COVID-19 protection)”  Where the claim ‘approximately one year of COVID-10 protection’ comes from is anyone’s guess.

Meanwhile, the World Economic Forum’s CommonPass [for the commoners] is being tested for international flight travel. The CommonPass takes traveler’s vaccine status or Covid test and prints out a scannable QR code used by airlines or border officials.

Then there’s Microsoft founder and not a doctor Bill Gates who previously claimed countries could be back to normal by “late 2021” if a vaccine is found. The Sun reports that Gates will meet with UK Prime Minister Boris Johnson to “plan a national vaccine rollout plan with the pharma giants.”

Johnson has taken criticism for announcing a second lockdown, a move he deemed a ‘nuclear deterrent’ not to be embarked upon again after the collateral damage and life-years-lost recorded from the first round of UK lockdowns.

Even the notorious Dr. Fauci’s flip flops are now openly abusive as he ratchets up the rhetoric. Fauci recently stated the UK and US are countries that “have that independent spirit.” But now is the time to “do what you’re told” continued Fauci with an uncomfortable laugh.

Upon Pfizer’s latest press release, The Lancet’s editor-in-chief Richard Horton tweeted:

Unfortunately for many like Horton, the realization should be arriving that public trust may have never been a primary goal of vaccine-makers. Science™ regularly takes a backseat to profits and ethics [see Pfizer hit with $2.3B largest criminal fraud fine in history by Justice Department]. And even when proper science should be followed, it is often sidestepped. Regularly failing to use inert placebos during vaccine trials, using trial designs with obscenely short observation windows to monitor serious adverse events, refusing to conduct vaccinated vs unvaccinated trials to compare total health outcomes and deep conflicts of interest are all in a day’s work for vaccine makers.

It should be noted that one ofthe biggest retractions in modern history by a journal, The Lancet, happened on Horton’s watch. The investigation leading to the retraction wasn’t prompted by some internal watchdogs or misinformation czars, it was driven from public pressure by independent scientists and researchers.

Second waves of lockdowns are upon us. Many who thought the vaccine would return us to normalcy have had a rude awakening. Since we are given no clear exit plan by ‘officials,’ perhaps it’s time to make our own.

Connect with Jefferey Jaxen at The HighWire

 

cover image credit squarefrog / pixabay




Corona Investigative Committee Attorney Reiner Fuellmich w/ Patrick Bet-David: Powerful Conversation on Global Lawsuit Over Coronavirus

Corona Investigative Committee Attorney Reiner Fuellmich w/ Patrick Bet-David: Powerful Conversation on Global Lawsuit Over Coronavirus
Patrick Bet-David and Dr. Reiner Fuellmich discuss revelations around the covid narrative, including a breakdown of what’s really been going on and how we are going to hold the people who orchestrated all of this accountable.

 

German Lawyer Sues The World Over Coronavirus

by Patrick Bet-David, Valuetainment
November 13, 2020



Patrick Bet-David has a virtual sit down with consumer protection trial lawyer Reiner Fuellmich to talk about the Coronavirus and his work on the German Corona investigation committee.

Panic Paper (in German) https://bit.ly/3f3IZRF

About the guest: Dr Reiner Fuellmich is one of four members of the German Corona Investigative Committee, which since July 10, 2020, has been listening to large number of international scientists’ and experts’ testimonies, to find answers to questions about the pandemic, being asked by people worldwide.

 

Connect with Patrick Bet-David at Valuetainment or PatrickBetDavid.com

Connect with Dr. Reiner Fuellmich at Fuellmich.com

Connect with the Corona Investigative Committee at Corona Ausschuss

 

[As a service to protect truth from censorship & to share widely, mirrored copies of this video are available at Truth Comes to Light BitChute, Brighteon, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]


see related:

Dr. Reiner Fuellmich on The Corona Fraud Scandal | International Network of Lawyers Will Argue the Biggest Tort Case in World History




Medical Doctor/Manager for Wyoming’s State Public Health Department/Preparedness Unit Warns About Unfolding Medical Tyranny & Dark, Deadly History of Covid Vaccine Development

Medical Doctor/Manager for Wyoming’s State Public Health Department/Preparedness Unit Warns About Unfolding Medical Tyranny & Dark, Deadly History of Covid Vaccine Development
Dr. Igor Shepherd: Covid Vaccinations Are “Global Genetic Genocide” and “Biological Weapons of Mass Destruction”

 

Truth Comes to Light editor’s note: The article below is sourced from garydbarnett.com. The video is from Julie Formsby YouTube channel.  As is heard in the introduction to Dr. Igor Shepherd’s talk and further detailed in Gary Barnett’s article, Dr. Igor Shepherd’s scientific background, life experience and areas of study are extensive, beginning in communist Soviet Union.  In the video, Dr. Shepherd shares his background and offers his perspective on current events — tying in his knowledge of totalitarian government agenda, biological weapons and vaccines as tools for the tyrannical takeover and destruction of humanity.


Dr. Igor Shepherd’s Talk About the Horrors of a ‘Covid’ Vaccine

by Gary D. Barnett
November 15, 2020

 

Dr. Igor Shepherd is a medical doctor/manager for Wyoming’s State Public Health Department/Preparedness Unit, and is on the Covid response team.

I was able to have a conversation with Dr. Shepherd after he did a talk for “Keep Colorado Free and Open” this past Tuesday. Dr. Shepherd wrote to me, and I was able to get a copy of his important talk. He has taken great risk to do this talk about the horrors of this new ‘Covid-19’ vaccine, so I recommend that all watch and listen. It is a fairly long talk and questions are answered at the end, but it is worth every minute of your time. He calls them “Biological Weapons of Mass Destruction.”

Dr. Shepherd was born and raised in the Soviet Union, and became a Military Doctor in St. Petersburg, Russia, and studied under the Strategic Rocket Force. He is an expert today on bio-weapons, Chemical, Biological, Radiological, Nuclear, and high yield Explosives,(CBRNE) and Pandemic preparedness. His view is that these vaccines are very similar technology to the bio-weapon RND used to develop viral weapons. He fully understands that the plan of depopulation and mandatory vaccinations will be at our doorstep very soon, and is shocked that the American people are so passive concerning this enemy takeover. He believes that this fake pandemic is the means by which a communist global government will be ushered into existence; one that cannot be voted out. I agree with this thinking, as this technocratic takeover and economic destruction will be communistic in nature.

Copyright © 2020 GaryDBarnett.com




[As a service to protect truth from censorship & to share widely, mirrored copies of this video are available at Truth Comes to Light BitChute, Brighteon, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]

 

Connect with Gary D. Barnett

Video source: Julie Formsby
Original video title: 11.10.20 Keep Colorado Free & Open – Community Action Meeting – Dr Igor Shepherd




New Hampshire Releases Bombshell Report Questioning Safety Of 5G

New Hampshire Releases Bombshell Report Questioning Safety Of 5G

by Derrick Broze, The Last American Vagabond
November 12, 2020

 

A new report from the state of New Hampshire has concluded that the safety of 5G technology is a concern for the health of the people, the animals, and the environment.

On November 1, a 111-page report describing the health concerns associated with 5G technology was released by the New Hampshire Commission to Study the Environmental and Health Effects of evolving 5G technology. The report was released to New Hampshire Governor Christopher T. Sununu, Speaker of the House  Stephen J. Shurtleff, and President of the Senate Donna Soucy.

The recommendations include:

– state agencies include information on their websites regarding the dangers of radiofrequency (RF) microwave radiation from all sources;
– calling on state agencies to add warnings concerning newborns, young children and pregnant women;
– ensuring any new wireless antennae installation located on private property to be placed away from residences, businesses, and schools;
– encourage the deployment of fiber optic cables and wired connections;
– recommend that state agencies work with scientific experts to develop RF radiation safety limits to protect trees, plants, birds, insects, and pollinators

5G — or 5th generation cellular technology — is the name for the latest telecom technology upgrade. The new technology is expected to herald the beginning of Smart Cities, where driverless cars, pollution sensors, cell phones, traffic lights, and thousands of other devices interact in what is known as “The Internet of Things.” However, there have been a number of health and privacy concerns raised by opponents of the rapidly advancing 5G expansion.

These concerns led the New Hampshire house to pass HB 522 in 2019, a bill which created the commission, tasking it to “study the environmental and health effects of evolving 5G technology.” The Commission was made up of several legislators who are also medical doctors and engineers, a scientist with expertise in electromagnetic radiation, a  New Hampshire Town Councilperson and representatives from the New Hampshire Attorney General’s Office, Department of Health & Human Services and the Department of Business and Economic Affairs.

The Commission also featured members of the wireless industry, including the CTIA, the largest wireless industry lobby which has been instrumental in promoting 5G. The members of the industry signed onto the “minority report” that stated “the scientific consensus” is that wireless technology is safe. However, the “majority report” documents substantial scientific evidence finding harmful health and environmental impacts.

In early November, the commission concluded that the safety of 5G has “come into question because of the thousands of peer-reviewed studies documenting deleterious health effects associated with cellphone radiation exposure.” The majority of the commission voted in favor of sending 15 recommendations to the Governor.

The report also recommends US federal agencies coordinate “to protect people, wildlife, and the environment from harmful levels of radiation” and states that “until there is Federal action, New Hampshire should take the initiative to protect its environment.” The strongest call to action was a recommendation that a resolution be introduced to the House of the U.S. Congress to require the Federal Communication Commission (FCC) to commission an independent review of the current radiofrequency (RF)
standards of the electromagnetic radiation in the 300MHz to 300GHz microwave spectrum.

The 5G Commission’s goal was to answer several questions regarding the safety of 5G. The commission asked the following:

– “Why are the FCC radiofrequency exposure limits set for the United States 100 times higher than countries like Russia, China, Italy, Switzerland, and most of Eastern Europe?”

– “Why have more than 220 of the world’s leading scientists signed an appeal to the WHO and the United Nations to protect public health from wireless radiation and nothing has been done?”

– “Why have the cumulative biological damaging effects of ever-growing numbers of pulse signals riding on  the electromagnetic sine waves not been explored, especially as the world embraces the Internet of Things, meaning all devices being connected by electromagnetic waves, and the exploration of the number of such pulse signals that will be created by implementation of 5G technology?”

Devra Davis PhD, MPH, President of Environmental Health Trust, commended the state of New Hampshire for “taking the time to generate such an important and historic document.” Davis also called for reducing wireless exposure in light of the growing body of evidence. Davis has previously published research documenting the scientific evidence which indicates that radiofrequency radiation from mobile phones and other wireless devices is a possible human carcinogen and recently published a paper on cell phone radiation and colon cancer.

Davis and the Environmental Health Trust have also partnered with the Children’s Health Defense in a join lawsuit against the FCC. The suit, filed in July, accuses the FCC of failing to protect human health and the environment by dismissing scientific evidence of harm from wireless radiation. The suit alleges that the FCC violated numerous laws and ignored scientific evidence when it decided on December 4, 2019 that FCC radiofrequency-exposure limits and regulations provide adequate protection and thus, should not be updated.

New Hampshire is not the first state to call for independent study of 5G technology. Back in May 2019, the Louisiana House unanimously voted to have the Louisiana Department of Environmental Quality and the Department of Health study the effects of 5G technology on the environment and public health.

Corruption Written Into Law

According to the FCC’s regulations, local governing bodies are not allowed to consider health risks when making their decisions. This is because the federal law known as the Wireless Communications Act of 1996 prohibits local jurisdictions from considering perceived health effects when taking an action on a proposed facility. Instead, cities and towns can only regulate cell sites based on the aesthetics and placement of the devices.

This problem was only made worse in September 2018, when the FCC passed a new rule putting the federal government in complete control of the 5G rollout. In April 2019, President Trump issued an executive order stating that local and state bodies must now approve new 5G infrastructure within 90 days. The Trump administration also initiated a cap on the fees local governments can charge telecom companies wanting to install 5G technology.

Additionally, in early February 2019, the Senate Commerce, Science, and Transportation Committee held a hearing on the future of 5G wireless technology and its impact on the American people and economy. At the hearing, U.S. Senator Richard Blumenthal (D-CT) raised concerns about the lack of scientific research and data on the technology’s potential health risks. In early December 2018, Senator Blumenthal and California Representative Anna Eshoo held a press conference asking the FCC to provide evidence that 5G technology is safe

New York Congressman Thomas Suozzi also sent a letter to the FCC seeking answers about the technology. “Small cell towers are being installed in residential neighborhoods in close proximity to houses throughout my district,” said Rep. Suozzi in his letter“I have heard instances of these antennae being installed on light poles directly outside the window of a young child’s bedroom. Rightly so, my constituents are worried that should this technology be proven hazardous in the future, the health of their families and value of their properties would be at serious risk.”

New Jersey Congressman Andy Kim sent a letter as well, noting that, “Current regulations governing radiofrequency (RF) safety were put in place in 1996 and have not yet been reassessed for newer generation technologies. Despite the close proximity to sensitive areas where these high-band cells will be installed, little research has been conducted to examine 5G safety.” Oregon Representative Peter A. DeFazio, House Transportation and Infrastructure Committee Chairman, wrote a letter to FCC Chairman Ajit Pai and acting FDA Commissioner Sharpless regarding the status of the government’s research into the potential health effects of RF radiation and its relation to the FCC’s guidelines for safe human RF exposure levels.

Despite the growing concern from state representatives, scientists, health professionals and journalists, the FCC has wholeheartedly endorsed the rollout of 5G, claiming that there are no public health concerns. Additionally, many cities and localities are raising alarm bells due to the federal government and their partners in Big Wireless usurping local control of 5G expansion. The Mayor of Danville, California went so far as to admit that the city council had “lost control” of the 5G rollout to the federal government and Big Wireless.

One of the reasons for this outright corruption and ignorance of scientific data is found in the New Hampshire commission report. The report referred to the FCC as a “captured agency with undue industry influence,” citing the Harvard Press Book “Captured Agency: How the Federal Communications Commission is Dominated by the Industries it Presumably Regulates,” which compares the wireless industry to the tobacco industry.

It is this revolving-door relationship between Big Wireless and the U.S. government regulatory agencies that has corrupted the research around the dangers of radiofrequency radiation and placed the American people directly in harm’s way.

Connect with Derrick Broze at The Last American Vagabond and The Conscious Resistance




Liverpool Lockdown

Liverpool Lockdown

by Del Bigtree, The HighWire, with Jefferey Jaxen
November 13, 2020

 



Video available at The HighWire Brighteon & BitChute channels.

Aided by British military, Liverpool have initiated a mass covid testing program on its population, in an attempt “to control #Covid19”. No matter how often tests prove to be inaccurate, it doesn’t seem to be stopping governing authorities in Europe, and parts of the US, from tightening their grip on the people. But there is hope. True to the spirit and tradition of Liverpool lore, the people, and elements of the science and academia, are challenging the draconian measures.

#PilotProgram #Ethics #Covid19 #NurembergTrials #TestandTrace #Yeadon #Pollock #TrueImpact




Celeb Piers Morgan Awarded ‘Vaxhole of the Week’

Celeb Awarded ‘Vaxhole of the Week’

by Del Bigtree, The HighWire
November 13, 2020

 



Video available at The HighWire BitChute and Brighteon channels.

What is a #Vaxhole? A person who quotes vaccine safety science that does not exist. What compelled Del to resurrect this HighWire tradition? British reporter Piers Morgan posted a tweet about the #Covid19 Vaccine you have to see to believe.

#Vaxhole #VOW #PiersMorgan #VaxholeOfTheWeek #TheHighWire #DelBigtree #COVID19 #Vaccine

 




Ticketmaster Says No Vaccine, No Entry! What Was Once “Conspiracy Theory” Is Now Conspiracy Fact.

Ticketmaster Says No Vaccine, No Entry! What Was Once “Conspiracy Theory” Is Now Conspiracy Fact

by Dan Dicks, Press for Truth
November 13, 2020

 

Vaccine certificates and immunity passports were just “conspiracy theories” 6 months ago and now they’re conspiracy fact as IBM, the CDC and the WHO are conspiring together to mass inoculate as much of the population as possible with a COVID-19(84) vaccine. In this video Dan Dicks of Press For Truth explains why IBM is a terrible choice for third party data handling while proving that so called “conspiracy theories” are slowly becoming conspiracy facts as the powers that ought not to be incrementally crank up the heat in a boiling frog scenario that is starting to get extremely hot! 



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How They’ll Fake the Success of the COVID Vaccine

How They’ll Fake the Success of the COVID Vaccine

by Jon Rappoport, No More Fake News
November 13, 2020

 

I’ve described how the major clinical trials of the COVID vaccine are designed to prevent nothing more than a cough, or chills and fever [1] [2].

The whole plan to gain FDA approval of the vaccine is a stark fraud.

Now let’s move on to the next con: how to make it seem the vaccine is a roaring success.

Brief background: My readers know I’ve presented a complete case to show the SARS-CoV-2 virus was never proved to exist in the first place [3] [4] [5] [6] [7] [8] [9] [10]. So the whole idea of a vaccine is a non-sequitur, an absurdity. Likewise, the PCR test for “the virus” is a fraud on several levels [11]:

For example, the number of “cycles” for which the test is set is a key factor. Each cycle is a huge amplification of the tissue sample taken from the patient.

When you blow up that tissue sample above 34 cycles, you get gigantic numbers of false-positive results, even by the standards of the test. Fauci has admitted it. I’ve pointed out that FDA guidelines nevertheless recommend doing the test at up to 40 cycles. This alone explains reports of “rising COVID case numbers.”

Let’s say Pfizer and then Moderna win FDA approval to release their vaccines in the US. With the military doing the logistics of shipping, millions of doses move out, and soon, an extraordinary number of Americans are lining up to take the shot.

After a suitable period of time, the elite medical planners will change the way the PCR test is done. The number of cycles will be drastically reduced. That order will go out to labs in the US.

What does this mean? It means that far fewer positive test results will occur.

Therefore, the trend of “new COVID cases” will stop rising. It will level off, and then it will fall.

This rigging will be heralded as proof that that vaccine is producing a victory over the virus.

There is another strategy: change the definition of “a case of COVID.” Make the new definition, in terms of clinical symptoms, more restrictive. Something like this would do the trick: “The patient must exhibit a body temperature of at least 100 for 48 consecutive hours.”

That will automatically cause a significant drop in the number of cases. The drop will be attributed to the salutary effect of the vaccine.

For purposes of lockdowns and general clampdowns [12], to promote more fear and punish areas where the economy is “too open,” a reverse-technique can be applied:

Make PCR tests adjust their cycles UPWARD, thus producing huge numbers of positive results and “new cases.”

“Well, in South Dakota, we have to mandate at least 100,000 more vaccinations in each of the following ‘hot spots,’ where case numbers have suddenly escalated. And we must lock down those areas immediately…”

Needless to say, any and all serious harm and death caused by the vaccine anywhere will be attributed to “the pandemic disease.”

And there you have it. Simple, brutal, criminal, and controlled from the federal level. A strategy for making it seem the COVID vaccine is effective, and saved the day.


Here is a backgrounder I wrote on the subject of COVID vaccine fraud:

Making a vaccine look like it’s a champion isn’t difficult for public health agencies. There are a number of strategies.

Of course, these fraudulent strategies would be serious crimes. But when has that stopped the CDC or the World Health Organization?

In no particular order—-

ONE: Rework the definition of a “COVID case.” Presently, the CDC absurdly allows doctors to diagnose a person with COVID who has a cough, or chills and fever, and lives in an area where cases are being claimed. No test necessary.

So change this practice, once the vaccine is approved. Demand testing for a diagnosis. State that cough alone is not enough. Chills and fever must also be present. Require fever to be above 100.

These and other changes would automatically shrink the number of cases. The drop in numbers would be attributed to the vaccine.

This “definitional shrinking” was, in fact, deployed in the 1950s, after the introduction of the polio vaccine.

TWO: Order a change in the way the PCR diagnostic test is done. The practice of amplifying the original test sample from the patient occurs in cycles, or jumps. The greater the number of cycles, the more likely the test will result in a COVID diagnosis. Therefore, order a reduced number of cycles for all testing labs.

Outcome? Fewer COVID diagnoses. Fewer case numbers. “The vaccine is working.”

THREE: Quietly restrict the present hospital practice of arbitrarily writing “COVID” on patient case and death files.

FOUR: Cook up and publish false studies showing more and more people are developing immunity to the virus. Attribute this to the vaccine.

FIVE: Another type of false study—“the transmission of the virus from person to person is slowing, thanks to the vaccine.”

SIX: Pump up the success of issuing Immunity certificates after vaccination. “People are feeling safer now. More businesses are reopening…”

SEVEN: Using the compliant press, simply issue bald declarations that the vaccine is a success.

EIGHT: Hide the many instances of injury and death from the vaccine. When necessary, claim COVID was the cause.

NINE: Warn that the wonderful vaccine-derived immunity is not permanent, and frequent booster shots are necessary.

TEN: Rework the definition of “vaccine-acquired immunity.” Even a very weak antibody response from the shot would qualify as “protective immunity.”

ELEVEN: Huge numbers of people with ordinary flu-like illness, pneumonia, and other traditional lung infections are being called “COVID.” Change this practice. Go back to calling many of these people “flu,” “pneumonia,” etc. COVID case numbers will drop. Claim the drop is the effect of the vaccine.

TWELVE: Presently, millions of so-called COVID cases have “co-morbidities.” These are prior serious health conditions which are, in fact, the true causes of illnesses and death. Of course, this is denied. But after the vaccine is introduced… scale back the practice of counting all these ill and deceased co-morbid patients as “COVID.” Case and death numbers will drop. Claim the vaccine is the reason.

THIRTEEN: After the vaccine is introduced, slow down testing for a brief period. This will automatically reduce the rate of new cases. Attribute the decline to the vaccine.

Committing these crimes are a walk in the park for public health agencies.

And appointing official mouthpieces to carry lies to the public is as easy as training little Faucis to sit up and bark.


SOURCES:

[1] https://blog.nomorefakenews.com/2020/11/11/covid-vaccine-revelation-sinks-like-a-stone-disappears/

[2] https://blog.nomorefakenews.com/2020/09/24/covid-vaccine-clinical-trials-doomed-to-fail-fatal-design-flaw/

~

[3] https://blog.nomorefakenews.com/2020/10/08/the-smoking-gun-where-is-the-coronavirus-the-cdc-says-it-isnt-available/

[4] https://blog.nomorefakenews.com/2020/10/09/covid-the-virus-that-isnt-there-the-root-fraud-exposed/

[5] https://blog.nomorefakenews.com/2020/10/12/the-fake-coronavirus-and-the-missing-study-the-secret-in-plain-sight/

[6] https://blog.nomorefakenews.com/2020/10/13/yet-another-case-of-the-missing-virus-they-lied-and-locked-down-the-world/

[7] https://blog.nomorefakenews.com/2020/10/15/if-the-virus-isnt-there-why-do-they-believe-it-is/

[8] http://blog.nomorefakenews.com/2020/10/19/dr-tom-cowan-explores-the-covid-virus-invented-out-of-sheer-nonsense/

[9] https://blog.nomorefakenews.com/2020/10/22/the-virus-that-isnt-there-genetic-sequencing-and-the-magic-trick/

[10] https://blog.nomorefakenews.com/2020/10/26/the-missing-virus-answering-critics-objections/

~

[11] https://blog.nomorefakenews.com/2020/11/06/smoking-gun-fauci-states-covid-test-has-fatal-flaw/

[12] https://www.rt.com/usa/506308-biden-covid19-advisor-lockdown/




Dr. Tom Cowan: Vulnerable People MORE Likely to Get Sick if People Around Them Are Wearing Masks

Dr. Tom Cowan: Vulnerable People MORE Likely to Get Sick if People Around Them Are Wearing Masks

by Dr. Tom Cowan, MD
November 12, 2020

 



Original video is available at Dr. Tom Cowan YouTube channel.

[As a service to protect truth from censorship & to share widely, mirrored copies of this video are available at Truth Comes to Light BitChute, Brighteon, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]

[Truth Comes to Light editor’s note: You can download a copy of the article mentioned by Dr. Tom Cowan here: Masks Don’t Work by Denis G. Rancourt, PhD — Download PDF  ]


cover image credit Candid_Shots / pixabay




David Icke w/ Dr. Tom Cowan: Truth About Viruses & Bacteria, the Body as a Living Crystal, Your Heart Is Not a Pump & the Contagion Myth

David Icke w/ Dr. Tom Cowan: Truth About Viruses & Bacteria, the Body as a Living Crystal, Your Heart Is Not a Pump & the Contagion Myth

by David Icke with Dr. Tom Cowan, MD
November 11, 2020

 

 

Original video available at David Icke BitChute channel.

[As a service to protect truth from censorship & to share widely, mirrored copies of this video are available at Truth Comes to Light BitChute, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]

Connect with Dr. Tom Cowan, MD

Connect with David Icke




The Contagion Fairy Tale

The Contagion Fairy Tale

by Thomas Cowan, MD and Sally Fallon Morell
November 10, 2020

 

Our book, The Contagion Myth, is now available (banned on Amazon but sold on other outlets) and has already generated dozens of comments, many of them challenging our contention that the corona “virus” does not exist and that the illness attributed to this virus is not contagious—one referred to our book as a fairy tale!

However, unlike most coronavirus skeptics, we are not arguing that the illness is just a bad case of the flu, with deaths due solely to pre-existing conditions or inappropriate hospital care; rather we postulate that the illness can be very serious and that the likely cause is radiation poisoning, probably from the worldwide deployment of 5G, starting in Wuhan, China and followed by major cities throughout the world.

Comments we have received include the following:

  • Okinawa does not have 5G but people are getting infected there;
  • Some friends went to a wedding in Kirkland, Washington and got Covid, so it must be infectious;
  • There’s 5G in New Zealand but very few cases of illness;
  • A school in our neighborhood has opened for in-person classes and there has been an outbreak—two people have tested positive;
  • A lot of people “got the virus” after a big no-mask motorcycle rally in Sturgis, South Dakota;
  • What about rabbits getting myxomatosis, a known viral disease.

With the exception of the rabbit comment (a subject to be explored in a future blog), these observations are just that—epidemiological observations, which are certainly interesting and deserve further exploration, but these in no way disprove our main contention that this virus does not exist and the illness attributed to it is not contagious.

Why take our word for the shocking claim that no scientist has found the so-called coronavirus?  Of course, you shouldn’t take our word for it, you should listen to what the experts are saying.  In July 2020, the FDA posted a CDC document entitled “CDC 2019-Novel Coronavirus (2019-nCoV), Real-Time RT-PCR diagnostic Panel. For Emergency Use Only. Instructions for Use.” Buried in the text, on page 39, is the following statement: “. . . no quantified virus isolates of the 2019-nCoV are currently available.”

In other words, our government is telling us that there are no purified isolated samples of this “novel coronavirus,” which means that the virus has never been isolated and purified.  What they are finding in the RT-PCR tests are fragments of genetic material, which actually come from human chromosome #8. This means that the results of all RT-PCR tests are invalid—the only thing they can tell us is that we are human beings.

A January, 2020 paper on testing tells us the same thing: “The ongoing outbreak of the recently emerged novel coronavirus (2019-nCoV) poses a challenge for public health laboratories as virus isolates are unavailable. . . [emphasis added]” Nevertheless, even without knowing what this virus is like, the researchers aim “to develop and deploy robust diagnostic methodology for use in public health laboratory settings without having virus material available.” A challenge indeed!

Here is an analogy to describe what is going on.  Let’s say you are a paid Lego specialist and someone offers to reward you if you can construct an exact replica of King Beauregard’s Medieval castle.  The referees put all the known Lego pieces out on a table and promise to pay you well to do the reconstruction. Naturally, you ask to see a picture of what the castle looked like or at least some sort of architectural plan so you know what to build.  But the referees say that you must reconstruct the castle without having access to any information about the original castle.  You think this is downright bizarre, but since a job is a job, you start looking.  You find pieces for a moat; you know that castles have moats and think that this must be part of the castle.  Then you find windows, turrets, soldiers, etc.–with each new finding you are given a castle-building Lego award and an increase in salary.  You write some software that fills in the rest of the castle from the fragments you have. Then you publish a peer reviewed paper on the “completed” castle for all the world to see.

Unfortunately, a child appears who looks like he has time traveled from the Middle Ages.  You show him the castle.  “Everybody knows that Beauregard didn’t have a castle.” He says.  “Beauregard was an impoverished aristocrat who was afraid of moats; he lived in a garret in London.”  But the show must go on, so his remarks are never published, while the Lego expert (who knows the child is right) keeps quiet and enjoys his hefty salary.

A number of readers have sent us studies “proving” the existence of pathogenic viruses.  In fact, one virologist claimed that “thousands of papers” show that isolated bacteria or viruses cause disease. (He also tried to convince us that one could sterilize one’s hands, cover them and they would remain sterile “indefinitely.”)

One was a link to a study with the promising title “Koch’s postulates fulfilled for SARS virus”, published 2003 in the prestigious journal Nature. We discuss this study in The Contagion Myth. The researchers claim that Severe Acute Respiratory Syndrome (SARS) is also caused by a coronavirus. The title itself is misleading, not to say fraudulent, because the researchers did not satisfy Koch’s postulates—which is the common-sense way of proving that a microbe causes disease. They did not satisfy River’s postulates either—River’s postulates are for proving that a virus causes a disease. These methods involve isolating and purifying a specific microbial organism from a number of individuals suffering from a specific disease and injecting the isolated, purified bacteria or virus into healthy organisms (animal or human). If every sick person has the organism and every test subject becomes ill, then you know that the specific microbe causes the specific disease.

Let’s focus on the process of isolating and purifying a virus—it’s hard to do but not impossible.  In 1973, the Pasteur Institute published guidelines for doing this. First the virologist takes mucus or secretions from a person with the disease.   The secretions are diluted and then put into a kind of blender. The resultant liquid is then passed through a very fine filter—fine enough to keep out bacteria and fungi but let the viruses through; the resulting liquid is called a supernatant. It contains the virus but also lots of other stuff as well. The supernatant must then be centrifuged in such a way that you get bands of particles of the same size and weight.  The scientist can determine which band is the virus using the known size and weight of viruses.  This band is removed from the supernatant with a pipette. This is the properly isolated and purified virus.  The virus is then transferred to some tissue to grow and multiply.

An important point is that when the virologist has finished the purification process of macerating, filtering and ultracentrifugation, he must then take an electron micrograph of the final, purified virus to show his colleagues that he has in fact successfully purified and isolated the virus.  Virologists have done this many times and for many different viruses.  Without an electron micrograph picture showing purification, no reputable journal would publish this work. The reason is simple: scientists are essentially told not to believe each other because someone says so.  If you say you isolated a virus you must show the picture to prove it, period.  Absent the picture it could be a total fabrication.  The way science is supposed to work, after you have isolated and photographed the virus, other scientists in other labs follow the exact steps that you outlined in your paper and show pictures of the same isolated virus.  Once a number of labs have done this, you have real proof that the virus exists.

In the case of the novel corona virus, every single published photograph we have seen showing the “isolated” virus shows no such thing.  Instead, it shows tissue with a number of dots, usually with an arrow pointing to the so-called coronavirus.  If you see tissue in the photograph, by definition, it’s not isolated.  An example of such a photograph comes from “Virus Isolation from the First Patient with SARS-CoV-2 in Korea,” published February 24, 2020 in the Journal of Korean Medical Science. Although the authors claim to have isolated the virus, the photographs they publish show “virus” structures inside and outside a cell (indicated by arrows), not isolated.

You can see a properly isolated “virus” in the electron microscopy image of the chicken pox “virus,” below. (By the way, although health officials claim that chicken pox is “highly contagious,” no studies have shown that exposing people to isolated chicken pox virus makes them sick.)

What virologists do today is use the liquid—called the supernatant–after either filtration or centrifuging to get rid of the bacteria, fungi and other larger material.  This is what they refer to as “purification.” This is like filtering the grounds out of coffee to get caffeine so you can study its effects.  But there are hundreds or thousands of other compounds in the coffee, so you still need to isolate the caffeine.  What the researchers should then do is put the supernatant in what’s called a sucrose density centrifuge column, which spins out the various compounds into bands.  One of these bands will contain the pure virus, which can then be photographed and analyzed.

Instead of working with pure virus, researchers use the supernatant, which contains all kinds of molecules and particles. Instead of doing a genetic analysis of the isolated virus, they do genetic analysis on the mess of compounds in the supernatant.

Now to get enough “virus” to use experimentally, virologists must grow it in a biological medium such as an animal or at least cells from an animal.  Unlike bacteria, which can be grown in petri dishes, viruses are not alive and can only “grow” in other living cells.

So they transfer the supernatant not to healthy tissue, but to tissue that has been starved of nutrients and poisoned with strong antibiotics—to make sure that what is left is only viruses and not bacteria and fungi.  The main type of tissue they use is kidney cells from various species, often monkey kidney cells (called Vero cells), and lung cancer cells. The “viruses” seem to multiply.  The resultant mess of “viruses,” particles, poisons, dead tissue and cellular debris—called “cultured” virus– is then sold to researchers as samples of “purified virus” for them to use in studies.

By the way, the CDC has published guidelines on “transport medium” for viruses.  This is what they use to inoculate the starved tissue which then grows the “virus.”  The three main ingredients are fetal bovine serum (extracted from still-living fetal calves and preserved with anti-fungals, among other poisons) along with two highly toxic antibiotics, amphotericin (affectionately called ampho-terrible) and gentamicin.  This ungodly mixture is then grown on monkey or fetal kidney cells.  Interestingly, all doctors know that the main organ affected by gentamicin and ampho-terrible is the kidneys.  So you poison the kidney, the kidney breaks down and then the virologist claims that the virus killed the kidney—without performing any controls. Don’t look behind the curtain, folks!

This practice is fraught with obvious problems for proving it is the virus and not the cancer cells or poisoned kidney cells that are causing disease when these viruses get injected into healthy test animals.

Remember that to prove that a specific virus is making humans or animals sick, they need to find the identical virus in many subjects who are sick with the same symptoms—and then make healthy humans or animals sick by exposing them to this virus.  But when researchers try to grow the purified virus on healthy cells, they don’t get a lot of viruses; and when they subject healthy tissue, healthy animals or healthy people to these “viruses,” illness does not result—and this is the wily virus that is going to kill us all!

Why do “viruses” multiply in the starved and poisoned kidney or cancer cells? Because when cells are starved or poisoned, they produce exosomes, which are identical in appearance and characteristics to what are called “viruses.” These tiny particles are helpful, not toxic.  They do not attack the cells and then multiply; rather, they are produced inside the cell, often in large amounts, when the cells are stressed by poison and starvation.

Viruses and exosomes are indistinguishable, as we learn from a study entitled “The Role of Extracellular Vesicles as Allies of HIV, HCV and SARS viruses,” published in the journal Viruses, May 2020.  To quote from the paper, “The remarkable resemblance between EVs [extracellular vesicles, that is, exosomes] and viruses has caused quite a few problems in the studies focused on the analysis of EVs released during viral infection.  Nowadays it is an almost impossible mission to separate EVs and viruses by means of canonical vesicle isolation methods, such as differential ultracentrifugation, because they are frequently co-pelleted due to their similar dimensions.  To overcome this problem, different studies have proposed the separation of EVs from virus particles by exploiting their different migration velocity in a density gradient or using the presence of specific markers that distinguish viruses from EVs.  However, to date, a reliable method that can actually guarantee a complete separation does not exist [emphasis added]. “

In other words, researchers can’t distinguish viruses from exosomes—that’s because they are the same thing and in reality, all viruses are exosomes.  Scientists are discovering that all of these “viruses” originate in our own tissues—they don’t attack us from the outside.

With this background, let’s then look at the study, “Koch’s Postulates fulfilled for SARS Virus.” The researchers took unpurified sediment from the snot of sick people, grew that in lung cancer cells until they got a sufficient quantity of cellular material to work with.  Then they centrifuged this mess again, not even attempting to purify any virus from the mixture.  Finally, they took this unholy mixture of snot sediment, lung cancer cells and who-knows-what-else and injected that into two unfortunate monkeys.  They didn’t do a control group by injecting saline into other monkeys or injecting lung cancer cells into monkeys or even injecting the liquid from the centrifuged material into monkeys. They just injected the cellular-debris-laden goop.  One of the monkeys got pneumonia, the other got a rash. That, claim the researchers, is the proof that a “coronavirus” can cause disease and that Koch’s postulates have been satisfied.

The Coronavirus Unveiled,” appearing in the New York Times, gives the impression that researchers are working with a genuine isolated coronavirus. Nevertheless, the article tells us that “In February, as the new coronavirus swept across China and shut down entire cities, . . . the best pictures anyone had managed to take were low-resolution images, in which the virus looked like a barely discernible smudge.”

How did the researchers isolate the virus?  They “doused the viruses with chemicals to render them harmless. . .” In other words, they poisoned them.  Then they somehow “concentrated the virus-laden fluid from a quart down to a single drop” after which they flash froze the drop. Then in the microscope they saw structures they called viruses.

This is not the proper way to isolate and characterize a virus, either.  Proper isolation involves ultrafiltration and centrifuging–not dousing with chemicals and flash freezing–and then performing various physical, biochemical and immunological analyses.

After seeing these particles—most likely helpful exosomes responding to the poisonous chemicals–the researchers state that “its intimately twisted genes commandeer our biochemistry [and] wrenches into our cellular factories, while others build nurseries for making new viruses.” This is highly imaginative horror-movie speculation, not science.

Virologist have three “hosts” they can use in their attempts to prove that viruses cause illness.  After “isolating” the virus, they can expose humans to the virus; they can expose animals to the virus; or they can use tissue cultures taken from various animal or human sources and expose the tissue culture to the virus.  Leaving aside the fact that they never actually isolate and purify the virus, which they openly admit, let’s assume that the unpurified fluid they are using does contain the relevant virus and therefore should be able to transmit infection.   I

In the history of virology, most virologists have decided not to do their experiments on human subjects as this is considered unethical.  In the case of the SARS-CoV-2 virus, we know of no published study that used humans as the test subjects.

Virologists also admit that in the case of most viral infections, there are no studies available proving infection in animals.  How a virus can infect and kill humans but not animals is left unexplained. Researchers get around this obvious biological conundrum by saying, “there are no animal models on which to test such-and-such a virus.” In other words, “We know that the virus infects and kills humans even though we’ve never tested the virus on humans because that would be unethical.  Therefore, we do our tests on animals, even though when we test animals. they don’t get sick, because they are not proper “hosts” for the virus. So, you’ll just have to trust us.”

In the case of SARS CoV-2, we know of two studies that used unpurified “virus” on animal models, one with hamsters and one with mice. In the hamster study, researchers took the unpurified, lung-cancer-grown, centrifuged animal secretions and squirted it down the throats and into the lungs of a group of unfortunate hamsters.  Some but not all of the hamsters got pneumonia and some even died.  We have no idea what would have happened if they had squirted plain lung cancer cells into the lungs of these hamsters, probably not anything good.  Even more perplexing, some of the hamsters didn’t even get sick at all, which certainly doesn’t square with the deadly contagious virus theory.

In the mouse study, researchers infected both transgenic mice and wild (normal) mice with unpurified virus.  None of the wild mice exposed to the “virus” got sick.  Of the mice genetically programmed to get sick, a statistically insignificant number either lost some fur luster or had an insignificant weight loss.  Thus, scientists have not been able to show that the Covid-19 “virus” causes harm to animals.

The third choice for virologist is to infect human and animal tissue with a “culture” of the virus to see what happens.  This is what they did in a study entitled, “Severe Acute Respiratory Syndrome Coronavirus 2 from Patient with Coronavirus Disease,” published in the CDC Bulletin, June 2020.

The purpose of the study was for a group of about twenty virologists to describe the state of the science dealing with the isolation and purification, and the biological characteristics of the new SARS-CoV-2 virus, and to share this information with other scientists for their own research. A thorough and careful reading of this important paper reveals some shocking findings.

First, in the section titled “Whole Genome Sequencing,” we find that rather than having isolated the virus and sequencing the genome from end to end, they “designed 37 pairs of nested PCRs spanning the genome on the basis of the coronavirus reference sequence. . . “ This means they actually looked at a mere thirty-seven primers out of the approximately thirty thousand base pairs claimed to be the genome of an intact virus.  They then took these thirty-seven segments and put them into a computer program, which filled in the rest of the genome.

This computer-generation step—called “whole genome sequencing”–constitutes scientific fraud of the highest order. Here is an equivalency: a group of researchers claim to have found a unicorn because they found a piece of a hoof, a hair from a tail, and a sliver of a horn. They then put that information into a computer and program it to re-create the unicorn, claiming that this computer re-creation is the real unicorn. Of course, they have never actually seen a unicorn so could not possibly have examined its genetic makeup to compare their samples with the actual unicorn’s hair, hooves and horn.

The researchers claim they decided which is the real genome of SARS-CoV-2 by “consensus,” sort of like a vote.  As different computer programs will come up with different versions of the imaginary “unicorn,” they come together as a group and decide which is the real imaginary unicorn. (By the way, this is how scientists characterized the measles “virus”—by consensus!)

But the real blockbuster finding in this study comes later, a finding so shocking that it’s hard to believe what we are reading.  “Therefore, we examined the capacity of SARS-CoV-2 to infect and replicate in several common primate and human cell lines, including human adenocarcinoma cells (A549), human liver cells (HUH 7.0), and human embryonic kidney cells (HEK-293T).  In addition to Vero E6 and Vero CCL81 cells . . .  Each cell line was inoculated at high multiplicity of infection and examined 24h post-infection.”

This is the third method virologists use to prove infection and pathogenicity — the method they usually rely on—namely, the inoculation of solutions they say contain the virus onto a variety of tissue cultures. As we have pointed out, such inoculation has never been shown to kill (lyse) the tissue, unless the tissue is first poisoned and starved (grown in a “minimal-nutrient medium.”)

In the Results section, the authors state: “Therefore, we examined the capacity of SARS-CoV-2 to infect and replicate in several common primate and human cell lines, including human adenocarcinoma cells (A549), human liver cells (HUH7.0), and human embryonic kidney cells (HEK-293T) . . . Each cell line was inoculated at high multiplicity of infection and examined 24h post infection.  No CPE was observed in any of the cell lines except in Vero cells.”

Note, CPE means “cytopathic effect,” which refers to structural changes in host cells that are caused by “viral invasion.” The infecting virus is said to cause lysis (breaking up) of the host cell or, when the cell dies without lysis, an inability to reproduce. Both of these effects are said to occur due to CPEs.

So did this viral material with its “intimately twisted genes commandeer the cellular biochemistry [and] wrench into the cellular factories, while others build nurseries for making new viruses?” Nothing of the sort!

The shocking thing about the findings is that using their own methods, the virologists found that solutions claimed to contain SARS-CoV-2 (as well as poisons)—even in high amounts –were not infective to any of the three human tissue cultures they tested.  In plain English, this means they proved, on their terms, that this “new coronavirus” is not infectious to human beings.  It is only infective to monkey kidney cells, and only when you add two potent drugs (gentamicin and amphotericin), known to be toxic to kidneys, to the mix.

Interestingly, in their conclusion the authors don’t mention this important fact. Only virologists reading the whole paper will find out that if you want to grow the virus, don’t bother to use human cell lines.

Meanwhile we have worldwide lockdown predicated on the idea that something called coronavirus causes disease.   As you can read, in all three of the human cell lines no CPE (no cell death, no infection) was observed.  Only Vero cells (monkey kidney cells) were adversely affected—and remember, the material injected into these cells contained kidney toxins.  So basically, they proved that the SARS-CoV-2 virus does not infect human tissue.

Another study sent to us comes with the fancy title,  “A Novel Chimpanzee Adenovirus Vector with Low Human Seroprevalence: Improved Systems for Vector Derivation and Comparative Immunogenicity.”

The researchers used “The wild type chimpanzee adenovirus isolate Y25 [which] was originally obtained from William Hillis, John Hopkins University of Medicine. The virus was passaged in HEK293A cells (Invitrogen, Cat. R705-07) and purified by CsCl gradient . . . Viral DNA was phenol extracted for genomic sequencing and cloning.”

The researchers purchased some material (not properly isolated even though it is called an “isolate”) which they then “passaged” through human embryonic kidney cells (called HEK293A), and then they “purified” it by CsCl gradient.  You can read about this technique here. It separates DNA molecules (not viruses) after mixing them with cesium chloride (a heavy metal salt) and ethidium bromide (a mutagen that can affect DNA biological processes, like DNA replication and transcription.)

This is the same smoke and mirrors—not true separation and isolation but “surrogate” techniques that use various poisons.

Another  study sent to us is entitled, “SARS-CoV-2 structure and replication characterized by in situ cryo-electron tomography,” published June 23, 2020. The authors begin with the creed of the faithful: “β-coronaviruses, including SARS-CoV-1 and Middle Eastern Respiratory Virus (MERS-CoV) are highly contagious pathogens that can cause severe lower respiratory infections. At the end of 2019, SARS-CoV-2 emerged in the city of Wuhan, China, likely through zoonotic transmission via a bat reservoir and a still unidentified intermediate host that subsequently led to a pandemic, accumulating to date to over 8 million cases and close to 500,000 deaths worldwide.”

The article provides no references for the statement that the SARS virus is “highly contagious” but does contain a lot of fuzzy electron-microscope photographs of tissues and cells whose genetic material they determined using PCR tests—the equivalent of finding moats and turrets in a bunch of Lego pieces.

The researchers did not isolate and purify the virus but instead used “monkey kidney derived VeroE6 cells” and “human pulmonary cell lines.”  In other words, they used cell lines grown in starved and poisoned cultures.

Later in the paper the authors state that they get different “morphologies” of the virus depending on which cell line they use.   In other words when grown on monkey kidney cells the virus looks one way, grown on lung cancer the same virus looks different.  That is like saying that if you plant some seeds in one garden you will get tomatoes but if you plant them in another garden you will get turnips.  What this observation tells us is that what they find comes from the tissue not the source “virus,” that is why they are different.

According to the authors, “Our report provides the first in situ cryo-ET analysis of coronaviruses at high preservation levels.” Wait a minute—this study was published on June 23, 2020. You mean they had no analyses of this virus before health officials called for universal lockdown?

By the way, Stefano Scoglio, PhD, from Italy, has come to the same conclusions that we have in a talk entitled “THE INVENTED PANDEMIC, the lack of VIRUS ISOLATION and the INVALID COVID-19 test.”

Says Scoglio, “At the center of the pandemic project stands the Covid swab test, which is based on the RT-PCR (Reverse Transcriptase- Polymerase Chain reaction): a sample of organic material is taken from the throat, or more rarely from the broncho-alveolar fluid, of the individual, and then the presence of the SARS-Cov-2 virus in the sample is tested. This is done by using the same RT-PCR methodology used to originally “isolate” the virus from patient zero. Thus, the Covid test depends essentially on the original isolation, or lack thereof, of the SARS-Cov2 virus, the original PCR isolation of the virus constituting the golden standard necessary to validate any subsequent Covid test. The problems with the original virus isolation, and thus with the ensuing swab test, are many, and they all point to the truth that the SARS-Cov2 virus has never been isolated and never tested for its pathogenicity.”

One argument we hear is that Koch’s postulates are irrelevant, out of date, useless or even “wrong.” If so, why do researchers claim to have satisfied Koch’s postulates, not only for Covid-19 but for other diseases like HIV/AIDS and Lyme’s disease.

For example, in 1997, scientists announced that human immunodeficiency virus (HIV) does fulfill Koch’ postulates and hence is the proven cause of AIDS.  The study involved taking the blood from an HIV-positive person and injecting it into one chimpanzee. They didn’t purify or isolate anything, just injected the blood into one chimpanzee. They kept the chimp for ten years–who knows what they fed it or anything about its conditions of confinement. After ten years the chimp developed an “opportunistic infection” (which could even be a yeast infection) and tested HIV-positive (a test result that occurs in at least thirty-three other conditions).  The study had no controls–like injecting the chimp with blood from someone with cancer or with blood from a healthy person.  This was the proof that HIV causes AIDS!  This is not science, but it keeps the grant money flowing.

With Lyme’s disease the “proof” that Koch’s postulates were fulfilled comes from a paper published in 1983, which reported detection of spirochete [spiral-shaped bacteria] in the blood of two patients with Lyme. The researchers then examined some ticks in the neighborhood and found the same spirochete.  That’s it, that was the “proof” of Koch’s postulates.

As we have explained, finding bacteria at the site of an injury or in a person with a disease in no way constitutes proof of causation any more than finding firemen at the site of a fire means they caused the fire.  Among other roles, bacteria act as scavengers in nature, they “eat” dead or diseased tissue.  Maggots play the same role; if you see a dead dog crawling with maggots, it would be crazy conclude that the maggots killed the dog. So why do scientists assume that the presence of “viruses” in a cell means that the cell has been attacked from the outside and taken over by hostile compounds?

If anyone can show us a properly done study in which the “coronavirus” from many sick people was isolated, purified, photographed and characterized according to the consensus agreement of the 1973 Pasteur Institute guidelines, and then shown to cause disease in healthy organisms (animals or humans), we will gladly withdraw the book. Meanwhile, we contend that the idea of a contagious coronavirus is a fairy tale.

 

The Contagion Myth is banned on Amazon but available at:

Dr. Cowan’s website https://drtomcowan.com/products/the-contagion-myth/

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RFK, Jr. w/ Dr. David Martin: Fauci’s “Sick, Demented” Criminal Ponzi Scheme, Dangerous Vaccines & Harmful Technology

RFK, Jr. w/ Dr. David Martin: Fauci’s “Sick, Demented” Criminal Ponzi Scheme, Dangerous Vaccines & Harmful Technology

 

TRUTH, with Robert F. Kennedy Jr., Season 2, Episode 8 featuring David E. Martin

by Robert F. Kennedy, Jr.,  Children’s Health Defense, with Dr. David E. Martin
November 8, 2020



Original video is available at Children’s Health Defense YouTube channel. If censored there, it will be found at childrenshealthdefense.org.

[As a service to protect truth from censorship & to share widely, mirrored copies of this video are available at Truth Comes to Light BitChute, Brighteon, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]

Description of video from Children’s Health Defense YouTube channel:

In the latest episode of our second season of “TRUTH” with Robert F. Kennedy, Jr., Kennedy interviews Dr. David Martin.

The two primarily discussed medical patents and the involvement from Dr. Anthony Fauci. Highlights of their conversation include:

– Breaking down Dr. David Martin’s company ‘M·CAM’ and how he found a way to put up intangible assets as collateral security.

– The Bayn – Dole Act that led to Fauci profiting from royalties off University patents.

– Fauci working for the NIAID but failing to study infectious diseases and allergies.

– Fauci involved in dodgy deals and price-fixing medicine in the USA.

– SARS vaccine patented in March 2019, 8 months before the COVID-19 outbreak.