In many states, minors may consent to receive COVID-19 shot even without parent’s knowledge
By Mordechai Sones | America’s Frontline Doctors | June 30, 2021
A District Administration survey conducted just before the FDA’s authorization for 12-15-year-olds to receive the COVID-19 shot found that only 3 in 10 parents said they would vaccinate their children right away, with most instead wanting to wait and see, or saying they would not get their child vaccinated at all or would do so only if required for school.
However, with the authorization of Pfizer’s shot for 12-15-year-olds, a group that totals almost 17 million, minors can consent to receive the COVID-19 shot even without the parent’s knowledge in many states.
The age at which a minor can consent to receive the experimental biological agent in Alabama is age 14; in San Francisco, 12; Philadelphia, 12; North Carolina, 11; South Carolina, 16. America’s Frontline Doctors (AFLDS) Legal Director Ali Schultz explained: “They can all consent, minors can consent, on their own, even if they live with their mom and dad who are married, they live with their parents, no issues, the child literally can consent at school to receive the vaccine, without the parents even knowing.”
She continued: “We’ve had so many people reach out, and they were just heartbroken, they cannot believe that their child was able to get this without them even knowing, because as parents they were personally against the vaccine, and no-one even ran it by them.
“And what’s even scarier: It’s up to the health care provider, in a multitude of states; Iowa, Idaho, Washington, Arkansas; so if a ‘health care provider’ deems that it is appropriate for a minor to get the vaccine, then they can do so without parental consent.”
According to District Administration, although most states still require parental consent, “the landscape may be shifting slightly as more jurisdictions seek to encourage vaccination of young people.” Their specific findings are as follows:
- Most states (41) require parental consent for vaccination of minors below the age of 18, although one of these states (NE) requires consent below age 19. There are some exceptions to these requirements:
- Many allow for certain minors, such as those who are emancipated, homeless or living apart from their parent or guardian, or married, to self-consent.
- Cities in two states (San Francisco in CA and Philadelphia in PA), have moved to allow minors, ages 12 and older, to self-consent for COVID-19 vaccination.
- In one state (AZ), if a parent refuses to consent for COVID-19 vaccination, but if a child or a doctor requests it, a court order can be obtained to allow for vaccination.
- In 5 states, a minor’s ability to self-consent is based on a specific age as follows:
- Two states where a minor must be at least 16 (RI and SC)
- One state where a minor must be at least 15 (OR)
- One state where a minor must be at least 14 (AL)
- One state where a minor must be at least 11 (DC; in DC, each healthcare provider may institute additional requirements which could include requiring a parent or guardian to be present).
- The remaining 5 states apply the “mature minor doctrine”, meaning that there is no specific age cut-off but providers have discretion to decide if a minor possesses the maturity to consent for themselves (AR, ID, NC, TN, WA).
- This means that parental consent has already been required for 16-17 year-olds in most states (41) since the initial authorization of the Pfizer vaccine on December 11, 2020. Two additional states require consent for some subset of 12-15 year-olds, bringing the count to 43 states where most minors in this age group would need parental consent. Once the next group of children is eligible for vaccination, those below age 12, this number will grow to 45.
National Vaccine Information Center‘s Barbara Loe Fisher commented on the “shifting landscape”: “This past year, we have seen many lawmakers in the U.S. and other countries vote to eliminate or severely restrict civil liberties in the name of the public health. One of the most outrageous legislative actions violating parental and human rights took place in Washington, D.C. in November 2020 when City Council officials gave doctors the power to vaccinate children as young as 11 years old and hide what they did from parents. The D.C. Mayor refused to veto the bill and, in January 2021, the U.S. Congress sat on its hands and gave tacit approval to enactment of the most dangerous child vaccination law in America.”
She continued: “In a breathtaking violation of medical ethics and several federal laws, the new vaccine concealment law in Washington, DC allows doctors to extract “informed consent” from young children too immature to know what informed consent means or what a vaccine reaction looks and feels like. The D.C. City Council majority, with only three members dissenting, cruelly disempowered parents by voting to make it illegal for a doctor, insurance company or school administrator to divulge a child’s vaccination history in records that can be seen by the child’s mother or father.
“An 11-year old child does not know or understand his or her personal health history but most parent do. If a child has experienced previous vaccine reactions, has severe allergies or other health conditions that could increase vaccine risks, parents kept in the dark will not have a way to protect their child from further harm.
“Parents who don’t know which vaccines their children have been given will not be able to monitor them for signs of a potentially life-threatening vaccine reaction that requires immediate medical treatment. If the child is injured or dies after vaccination, parents will not know they must apply to the federal Vaccine Injury Compensation Program (VICP) before the filing deadline expires.
“Parents will not know their insurance company has been billed for vaccines. Parents will not know that a school the child attends is in possession of their child’s secret vaccination records even when there is a vaccine exemption for religious belief reasons on file with the school.
“This blatant violation of a parent’s moral right and legal responsibility to make medical risk decisions on behalf of a minor child was endorsed by the American Academy of Pediatrics22 and pushed through by the DC City Council, while the Mayor and the US Congress looked the other way.”
She concluded: “The Universal Declaration of Bioethics and Human Rights states that:
“The interests and welfare of the individual should have priority over the sole interest of science or society;” and “For persons who are not capable of exercising autonomy, special measures are to be taken to protect their rights and interests;” and “Any preventive, diagnostic and therapeutic medical intervention is only to be carried out with the prior, free and informed consent of the person concerned, based on adequate information.”
“It is a profound betrayal of public trust for any city, state or federal government to strip parents of their God given right to protect their children from harm by allowing a doctor to give a child a pharmaceutical product without getting a parent’s permission. Science is not perfect, doctors are not infallible, and pharmaceutical products like vaccines come with risks that can be greater for some individuals than others, which is why parents must retain the human right to exercise informed consent to medical risk taking on behalf of their minor children.
“Will the vaccine concealment bill that is now law in Washington, DC be exported to your state next?”
Mercury News provided the list of where parental or guardian consent is now generally required for COVID-19 vaccinations among people ages 12 to 15, based on a CNN query to health departments across all 50 states:
- Alabama — Yes for younger than 14
- Alaska — Yes
- Arizona — Yes
- Arkansas — Yes
- California — Yes
- Colorado — Yes
- Connecticut — Yes
- Delaware — Yes
- Florida — Yes
- Georgia — Yes
- Hawaii — Yes
- Idaho — Yes
- Illinois — Yes
- Indiana — Yes
- Iowa — “It is up to each individual health care provider/health system”
- Kansas — Yes
- Kentucky – Yes
- Louisiana — Yes
- Maine — Yes
- Maryland — Yes
- Massachusetts — Yes
- Michigan — Yes
- Minnesota — Yes
- Mississippi — Yes
- Missouri — Yes
- Montana — Yes
- Nebraska — Yes
- Nevada — Yes
- New Hampshire — Yes
- New Jersey — Yes
- New Mexico — Yes
- New York — Yes
- North Carolina — No for teens
- North Dakota — Yes
- Ohio — Yes
- Oklahoma — Yes
- Oregon — Yes for younger than 15
- Pennsylvania — Yes
- Rhode Island — Yes
- South Carolina — Yes
- South Dakota — Yes
- Tennessee — Yes for younger than 14
- Texas — Yes
- Utah — Yes
- Vermont — Yes
- Virginia — Yes
- Washington — Yes
- West Virginia — Yes
- Wisconsin — Yes
- Wyoming — Yes
Additionally, some private businesses or pharmacies have their own rules.
Retraction of paper on vaccine deaths spurs call for more scrutiny of COVID-19 death reports
Medical journal sets much higher burden to show deaths from vaccine than from COVID, say authors of retracted paper.
By Greg Piper | Just the News | July 2, 2021
Should public health authorities scrutinize deaths attributed to COVID-19 as closely as they scrutinize deaths attributed to COVID-19 vaccines?
Defenders of a controversial study on the risk-benefit ratio of COVID-19 vaccines are calling hypocrisy on a medical journal for retracting the paper a week after publishing it, following the resignations of several journal editors in protest.
In a Friday retraction notice in the journal Vaccines, the editor in chief and “several” editorial board members said the paper’s authors were not able to “satisfactorily” answer claims that they conflated correlation with causation.
Analyzing data from the Netherlands Pharmacovigilance Centre, known as LAREB, the paper’s authors estimated COVID-19 vaccines take two lives for every three they save. The country leads Europe in vaccine adverse-reaction reporting.
Authors Harald Walach, Rainer Klement and Wouter Aukema challenged criticism from Eugene van Puijenbroek, who leads LAREB’s scientific department, that they had misused its data.
“This starts a long-overdue debate on how to gauge the safety of COVID-19 vaccines,” they wrote in a statement provided to Retraction Watch Thursday.
“Currently we only have association, we agree, and we never said anything else. But the same is true with fatalities as consequences of SARS-CoV2-infections [sic],” which are “rarely vetted by autopsy or second opinion” to confirm they were caused by the novel coronavirus, rather than incidental to infection.
Brown University epidemiologist Andrew Bostom wasn’t impressed by the journal’s “baloney” explanation for the retraction, either. “The [vaccine] deaths are as causally related as C19 deaths which allow for any positive test within 30-60 days of a death from any cause to be tallied as a C19 death,” he wrote in a Twitter message to Just the News.
Bostom pointed to a June study, not yet peer-reviewed, of a sample of deaths in the U.S. Vaccine Adverse Events Reporting System reported through April. The sample was limited to people who got early vaccinations, primarily elderly or those with “significant health conditions.”
Researchers at the University of London and New Zealand’s Massey University found that they could rule out “vaccine reaction” as a contributing factor in just 14% of deaths. “Contrary to claims that most of these reports are made by lay-people and are hence clinically unreliable, we identified health service employees as the reporter in at least 67%,” they wrote:
Correlation versus causation is also an ongoing issue in research on the effectiveness of masks in mitigating the spread of COVID-19. Commenters immediately challenged a Thursday report in MedPage Today on a study that purported to find masks effective in stopping in-school transmission, but had no control group of mask-optional schools.
‘Largest vaccination experiment in history of medicine’
The journal Vaccines was under internal pressure to retract the paper almost immediately. Two of its editors, virologist Florian Krammer and immunologist Katie Ewer, publicly announced their resignations on Twitter within three days of publication.
Science magazine reported four more resignations from Vaccines by July 1, including the journal’s founding editor in chief. Ewer made the same correlation-versus-causation argument and complained that the paper was “being used by anti-vaxxers and COVID-19-deniers as evidence that COVID-19 vaccines are not safe.”
Only one of the three peer reviewers was identified by name, Anne Ulrich, chair of biochemistry at the Karlsruhe Institute of Technology in Germany.
Her review said the authors made “plausible and convincing arguments” for why they chose the Dutch adverse-reaction data, and their analysis was “performed responsibly … without methodological flaws” and with “necessary caveats.”
After controversy, Ulrich told Science the analysis was done “responsibly and without flaws.” (One of the anonymous reviewers was confused why the authors compared the Dutch adverse-reaction data with “number needed to vaccinate” data from a large Israeli field study.)
The journal’s retraction said the paper’s authors reached “incorrect and distorted conclusions” by ignoring the caveats in LAREB, the Dutch reporting system.
Both “healthcare professionals and patients are invited to report suspicions of adverse events that may be associated with vaccination,” but “a causal relation” is not needed. It also said the paper falsely claimed “fatal cases were certified by medical specialists.”
After the journal announced the investigation, Aukema, one of the authors, tweeted that the Dutch reporting system was unlike most in the EU by “timely reporting” adverse reactions to the European Medicines Agency, “so theirs is the best data available.”
According to Science, LAREB official van Puijenbroek wrote to Vaccines the day after the paper’s publication, making the same arguments that appeared in the retraction. He did not respond to an email from Just the News asking for that message, which does not appear to be posted anywhere.
In the statement the paper’s authors gave Retraction Watch, they challenged van Puijenbroek’s characterization of the register’s data.
Just this spring, the LAREB official told the journal Regulatory Science that the Dutch register received more than half of its 34,000 adverse-reaction drug reports in 2019 from “marketing authorisation holders.” The rest came from “healthcare professionals and patients.”
The majority of reports came from parties who “by law, are required to report,” and LAREB says it checks all submissions for “completeness and possible ambiguities,” requesting additional information if necessary. If it’s treating COVID-19 vaccine reports differently, it should say so, the authors wrote.
Treating all deaths following COVID-19 infection as virus-caused deaths, which created a staggering official death toll, has given rise to “an unprecedented sloppy regulation process” that allowed the novel mRNA vaccine technology to be widely tested in humans for the first time, they wrote.
Van Puijenbroek is tacitly arguing that “the largest vaccination experiment in the history of medicine cannot be assessed for safety and unforeseeable toxicities,” but the authors believe “it is mandatory” to use existing “imperfect data” to gauge vaccine safety.
To conclusively end this debate, governments or “university consortia” should set up a transparent “systematic observational post-marketing surveillance study” across a large group of vaccinated people, they said.
mRNA technology pioneer blasts Big Tech censorship
Dr. Malone’s LinkedIn account was deleted
By Christina Maas | Reclaim the Net | July 2, 2021
Dr. Robert Malone, a pioneer of mRNA technology, is being censored by Big Tech platforms. According to Malone, the mRNA-based COVID-19 vaccines carry some risks that are being downplayed by public health bodies and his statements are coming up against ‘misinformation’ policies on many social media platforms.
Malone’s team conducted early research on mRNA back in 1990, showing that nanoparticles could transfect mRNA into cells before Hungarian biochemist Katalin Karikó worked on solving some of the obstacles in introducing mRNA into cells throughout the 90s.
Malone’s personal LinkedIn account was removed this week without warning or explanation.
“The historic record of what I have done, stated, figured out (and when) etc. over time is a key part of establishing my credibility and track record as a professional,” Robert Malone tweeted Wednesday. “And that has been erased completely and arbitrarily without warning or explanation.”
The premium LinkedIn account for the government and biotech consultancy business he runs with his wife Jill was not removed.
“He was given no notice, no warnings,” Jill wrote in a statement to Just the News. “He has a 10-15 year old account – has never even had a warning. 6,000 followers.”
It appears LinkedIn took issue with a recent post Malone made about Health Canada responding to the concerns he and other experts raised about the presence of the “spike protein” in the mRNA-based COVID-19 vaccines.
The Canadian health regulator warned about a small number of cases involving heart inflammation in young male adults and adolescents observed after receiving the Moderna and Pfizer-BioNTech vaccines.
In the since-unavailable post, Malone wrote: “This is certainly a big step forward in my opinion – particularly in contrast to the communication (or lack thereof) and denial from the US and other governments. At least we are now discussing the merits and limitations of the scientific data.”
The Microsoft-owned professional networking platform refused a request for comment on why Malone’s account was removed.
This was not the first time Malone was censored by a mainstream social media platform. A few days ago, YouTube removed an episode of the DarkHorse podcast, run by evolutionary biologist Bret Weinstein, where Malone warned about the spike protein in the coronavirus vaccines.
Following the removal, he appeared on Fox News and claimed that the CDC was yet to conduct “risk benefit analyses” of the vaccines, warning that in young people, the vaccines’ “benefits probably don’t outweigh the risks.”
YouTube demonetized the two channels that broadcast the DarkHorse episodes, a move Weinstein said would affect “more than half of our family income.”
According to Jill, YouTube “seems to be banning any content with him [Malone] in it.” She is of the opinion the platform is targeting her husband for contradicting the narrative by the WHO and CDC, which insist that the vaccines are safe.
According to Martin Kulldorf, a Harvard Medical Professor who was locked out of his Twitter account for a month for expressing skepticism on the effectiveness of masks, such censorship is dangerous.
Speaking to Just the News, Kulldorf said: “Open debate is especially important during a public health emergency when many important public health question[s] do not yet have a known answer.”
He said Big Tech platforms should reinstate all suspended accounts, because “To censor and silence scientists under such circumstances can lead to many unnecessary deaths.”
Petition to Halt FDA Approval of COVID Vaccines
By Dr. Joel S. Hirschhorn | July 3, 2021
In the global COVID pandemic there has not been a more important action to protect public health than the current Citizen Petition to FDA to stop the full approval of COVID vaccines until many serious concerns and issues are genuinely addressed.
There has been no significant coverage of this historic petition by mainstream and corporate social media. This cancel action is itself as remarkable as the petition itself. This is a concerted effort to keep the public uninformed about the many problems with the COVID vaccines. Any person who spends the time to peruse the 20-page petition would most likely have a very negative view of the vaccines. For the unvaccinated this awareness would greatly increase vaccine hesitancy and rejection. For the vaccinated it would produce concern and regret.
The political system would literally go crazy if the petition was seriously covered by big media. Big drug companies would jump into action to suppress political and media attention to the petition. The goal of this article is to better inform the public and motivate people to take action.
CONTEXT
Before delving into the substance provided in the petition context is needed to fully understand the critical importance of the petition and make the case for individuals to officially express their support for it as part of the federal regulatory process.
One rational reaction to reading the very detailed, 20-page petition signed by 27 physicians and medical researchers from the US and other nations is this: Why not use all the detailed concerns about the COVID vaccines to demand FDA take the experimental vaccines off the market?
Indeed, the biggest name on the list of signatories is the esteemed Dr. Peter McCullough of Baylor University. He has been very outspoken and honest about many pandemic issues. He has said that, considering the high numbers of deaths and serious health impacts associated with taking the vaccines, FDA should do what it has done in the past when new medicines and vaccines had high negative impacts. Take them off the market.
Why not petition FDA to do this? Just imagine what stopping the whole COVID vaccine effort worldwide would cause. Political and public health systems would not know what to do. They would be totally stunned and flummoxed. So, though the current petition does not do this, it definitely took considerable courage to make the case to FDA to not move quickly from an emergency use authorization to full approval of the COVID vaccines.
People who have not fallen victim to the endless propaganda of the political, big media and public health systems promoting COVID vaccine jabs may not be willing to seriously examine the medical and scientific details of the petition. The problem is cognitive dissonance. Too many people will not easily resolve their propaganda induced positive views of the vaccines with the medical and science details in the petition. But that is what must happen. People must temper their fear of COVID infection with awareness that vaccines are now experimental and have not been sufficiently proved safe for all users.
The potential frustration and fear if the vaccines were deemed insufficiently safe could be mitigated by advocating for early home/outpatient treatment and preventive use of a number of cheap, safe and fully approved generic medicines. The government and public health system have blocked their wide use in favor of the wait-for-the-vaccine strategy that serves the financial interests of vaccine manufacturers. As presented in detail in Pandemic Blunder and this website, there are mountains of medical evidence to justify the treatment protocols. They are legitimate, proven alternatives to experimental and insufficiently tested vaccines that might be fully approved by FDA.
To achieve true protection of public health we need an avalanche of official public support for the petition. More details later on how people can do this.
WHAT THE PETITION EMPHASIZES
A week after the June 1 petition, lead authors of the petition published an editorial in the British Medical Journal with the title “Why we petitioned the FDA to refrain from fully approving any covid-19 vaccine this year.” Here are some key statements that use plain language to summarize key parts of the petition:
“The message of our petition is ‘slow down and get the science right—there is no legitimate reason to hurry to grant a license to a coronavirus vaccine.’ We believe the existing evidence base—both pre- and post-authorization—is simply not mature enough at this point to adequately judge whether clinical benefits outweigh the risks in all populations.”
“We focus on methods and processes, outlining the many remaining unknowns about safety and effectiveness—and suggest the kinds of studies needed to address the open questions.”
“Trials by vaccine manufacturers were designed to follow participants for two years, and should be completed before they are evaluated for full approval.”
“We also call on FDA to require a more thorough assessment of spike proteins produced in-situ by the body following vaccination—including studies on their full biodistribution, pharmacokinetics, and tissue-specific toxicities.”
“We all agree that there remain many open, unanswered questions surrounding the efficacy and safety of covid-19 vaccines that must be answered before the FDA gives serious consideration to granting full approval.”
“Some surveys suggest that vaccine hesitancy in the United States is due, in part, to lack of full FDA approval. While approval might lead to increased public confidence in covid-19 vaccines, as well as provide legal support for employer-instituted vaccine mandates, to approve a medical product for these reasons is outside FDA’s regulatory purview. Approval decisions must be driven by the safety and efficacy data. The potential unintended consequences of a rushed approval may contribute to growing mistrust of the US public health and regulatory institutions.”
“For each covid-19 vaccine, the benefits may ultimately outweigh the harms. Or not. Or we may end up in a more nuanced position, finding that benefits outweigh harms for some populations, but not others. Only time—and better evidence—will tell.”
Now, some key parts of the petition itself are presented to further illustrate what medical and science perspectives have been formulated to pressure FDA to better evaluate the COVID vaccines.
A most important point made in the petition is this. Work must be done to show that there is “substantial evidence of clinical effectiveness that outweighs harms in special populations such as: infants, children, and adolescents; those with past SARS-CoV-2 infection; immunocompromised; pregnant women; nursing women; frail older adults; and individuals with cancer, autoimmune disorders, and hematological conditions.” This is so important because so many of the deaths and harmful impacts have occurred in these groups.
Most importantly: “The widespread use of a COVID-19 vaccine under EUA, particularly for a limited amount of time, also is not a valid reason to approve a product.”
And here is a critical point that many critics of the vaccines have focused on: “In-situ production of SARS-CoV-2 spike protein is the target mechanism of action of all COVID-19 vaccines with an EUA at present. Therefore, the safety profile of spike protein itself (i.e., in the absence of virus) must be thoroughly understood [in all populations]. Recently, evidence of systemic circulation of spike protein or its components in subjects post-immunization was reported. All studies we are aware of to date raise concerns about the safety of spike protein, and the concentration of circulatory spikes was correlated to the disease severity in COVID-19 patients.”
WHAT PEOPLE CAN DO
Though FDA cannot ignore the petition, there is no assurance that it will genuinely address all of the issues and concerns in it. Or that it will postpone approval of the vaccines until there is sufficient research and analysis into all the points in the petition.
It must be appreciated that the petition is authorized by federal law. The FDA citizen petition process, described in Title 21 of the Code of Federal Regulations (21 CFR Part 10), allows individuals and community organizations to request the agency make changes to health policy. Any “interested person” can request the FDA “issue, amend or revoke a regulation or order,” or “take or refrain from taking any other form of administrative action.” Granting full approval of the COVID vaccines is a major FDA administrative action with both national and global significance.
What is needed is a massive number of people officially registering their support of the petition on the proper FDA website. This can be done anonymously. Here are important links for the petition:
- The Citizen Petition (Docket ID: FDA-2021-P-0521)
- To comment on the petition
- To read others comments on the petition
- Main FDA docket for the petition (Docket ID: FDA-2021-P-0521)
Dr. Joel S. Hirschhorn, author of Pandemic Blunder and many articles on the pandemic, worked on health issues for decades. As a full professor at the University of Wisconsin, Madison, he directed a medical research program between the colleges of engineering and medicine. As a senior official at the Congressional Office of Technology Assessment and the National Governors Association, he directed major studies on health-related subjects; he testified at over 50 US Senate and House hearings and authored hundreds of articles and op-ed articles in major newspapers. He has served as an executive volunteer at a major hospital for more than 10 years. He is a member of the Association of American Physicians and Surgeons, and America’s Frontline Doctors.
Many medical organizations “cosign” CDC/HHS baloney about myocarditis being rare, mild.
Institutional capture on steroids
By Meryl Nass, MD | June 30, 2021
This statement alone is enough to make one give up entirely on American medicine. It drips with corruption. It provides no data, no useful information. It simply tells us that our tax dollars have been used to buy all these people and the once-upon-a-time meaningful organizations they represent. Whenever the spin doctors tell you “the facts are clear” and then omit the facts, run for your life!
I can’t tell you exactly what the HHS agenda is. I can’t tell you why they want us all jabbed, over and over again. I can only tell you it makes no medical sense, they are hiding the side effects, and these people are lying to us. Over and over. These people hid the effective treatments for Covid. They insisted we wear ineffective masks. They pretended there was no aerosol spread. They are not here to help us.
The following statement has been co-signed by the U.S. Department of Health and Human Services (HHS), Centers for Disease Control and Prevention (CDC), American Academy of Family Physicians (AAFP), American Academy of Pediatrics (AAP), American College of Obstetricians and Gynecologists (ACOG), American College of Physicians (ACP), American Heart Association, American Hospital Association (AHA), American Medical Association (AMA), American Nurses Association (ANA), American Public Health Association (APHA), Association of Public Health Laboratories, Association of State and Territorial Health Officials (ASTHO), Big Cities Health Coalition, Council of State and Territorial Epidemiologists, Infectious Diseases Society of America, and National Association of County and City Health Officials (NACCHO):
“As physicians, nurses, public health and health care professionals, and, for many of us, parents, we understand the significant interest many Americans have in the safety of the COVID-19 vaccines, especially for younger people. Today, the CDC Advisory Committee on Immunization Practices (ACIP) met to discuss the latest data on reports of mild cases of inflammation of the heart muscle and surrounding tissue called myocarditis and pericarditis following COVID-19 vaccination among younger people.
“The facts are clear: this is an extremely rare side effect, and only an exceedingly small number of people will experience it after vaccination. Importantly, for the young people who do, most cases are mild, and individuals recover often on their own or with minimal treatment. In addition, we know that myocarditis and pericarditis are much more common if you get COVID-19, and the risks to the heart from COVID-19 infection can be more severe.
“The vaccines are safe and effective, and they prevent COVID-19 illness. They will help protect you and your family and keep your community safe. We strongly encourage everyone age 12 and older who are eligible to receive the vaccine under Emergency Use Authorization to get vaccinated, as the benefits of vaccination far outweigh any harm. Especially with the troubling Delta variant increasingly circulating, and more readily impacting younger people, the risks of being unvaccinated are far greater than any rare side effects from the vaccines. If you get COVID-19, you could get severely ill and be hospitalized or even die. Even if your infection is mild, you or your child could face long-term symptoms following COVID-19 infection such as neurological problems or diminished lung function.”
“We recommend getting vaccinated right away if you haven’t yet. It is the best way to protect yourself, your loved ones, your community, and to return to a more normal lifestyle safely and quickly.”
Dr. Rachel Levine, Assistant Secretary for Health, U.S. Department of Health and Human Services
Dr. Rochelle Walensky, Director, U.S. Centers for Disease Control and Prevention
Dr. Ada Stewart, MD, FAAFP, President, American Academy of Family Physicians
Dr. Lee Savio Beers, MD, FAAP, President, American Academy of Pediatrics
Dr. Maureen G. Phipps, MD, MPH, FACOG, Chief Executive Officer, American College of Obstetricians and Gynecologists
Dr. George M. Abraham, MD, MPH, FACP, FIDSA, President, American College of Physicians
Dr. Mitchell S. V. Elkind, M.D., M.S., FAAN, FAHA, President, American Heart Association
Richard J. Pollack, President and Chief Executive Officer, American Hospital Association
Dr. Gerald E. Harmon, M.D., President, American Medical Association
Dr. Ernest J. Grant, PhD, RN, FAAN, President, American Nurses Association
Dr. Georges C. Benjamin, MD, Executive Director, American Public Health Association
Scott J. Becker, MS, Chief Executive Officer, Association of Public Health Laboratories
Dr. Michael Fraser, PhD, CAE, FCPP, Chief Executive Officer, Association of State and Territorial Health Officials
Chrissie Juliano, MPP, Executive Director, Big Cities Health Coalition
Janet Hamilton, MPH, Executive Director, Council of State and Territorial Epidemiologists
Dr. Barbara D. Alexander, MD, MHS, FIDSA, President, Infectious Diseases Society of America
Lori Tremmel Freeman, MBA, Chief Executive Officer, National Association of County and City Health OfficialsFor more information and resources on this rare side effect, visit CDC’s website here.
DC AG subpoenas Facebook for data on ALL users that have spread “COVID-19 misinformation”
Unmasking people for wrongthink
By Tom Parke | Reclaim the Net | July 2, 2021
The District of Columbia (DC) Attorney General (AG) Karl Racine, a Democrat, has subpoenaed Facebook for a wide range of records related to “COVID-19 misinformation” on the platform.
The subpoena was filed on June 21 and demands that Facebook identify all groups, pages, and accounts that have violated the platform’s far-reaching COVID-19 misinformation rules.
It also calls for Facebook to release an internal study that looked at vaccine hesitancy among its users. Media reports on this study in March claimed that it showed that non-rule breaking Facebook content may be causing “substantial” harm.
If Facebook were to comply with this subpoena, it would likely impact millions of users. Facebook has removed more than 18 million pieces of content from Facebook and Instagram for violating its COVID-19 misinformation rules and applied warning labels to more than 167 million pieces of COVID-19 content.
The subpoena is part of a previously undisclosed investigation into whether Facebook is violating consumer protection laws.
Racine’s director of communications, Abbie McDonough, told Politico that the investigation is part of an effort to ensure that Facebook cracks down on “vaccine misinformation.”
“Facebook has said it’s taking action to address the proliferation of COVID-19 vaccine misinformation on its site,” McDonough said. “But then when pressed to show its work, Facebook refused. AG Racine’s investigation aims to make sure Facebook is truly taking all steps possible to minimize vaccine misinformation on its site and support public health.”
The move follows previous reports of Democrats working with Big Tech to censor content that they deem to be misinformation.
Most notably, a recent lawsuit showed evidence of Democrats flagging alleged misinformation to Twitter via a “partner portal” and Twitter responding by removing the flagged tweets.
Another example of this is Democrats demanding that Facebook and Twitter “address” 12 prominent vaccine skeptics in April. Since they made their demands, four of these vaccine skeptics have had their social media accounts shut down.
Lawmakers have also suggested that the federal government may have “induced Facebook to censor certain speech in violation of the First Amendment” and demanded that the tech giant explain why it censored lab leak theories.
This attempt from the DC AG to identify Facebook users for posting COVID-19 misinformation comes as the tech giant is using increasingly aggressive measures to target people based on the content they share and interact with.
Yesterday, it started asking users whether they’re concerned about their friends “becoming an extremist” and warned users that they “may have been exposed to harmful extremist content.”
And in May, a whistleblower revealed that Facebook is using a secret internal filter to flag “liberty-based” and “religious-based” vaccine skepticism and using a secret algorithm to suppress negative vaccine experiences.
JCVI Scientist: “Let Kids Catch Covid Instead Of Jabbing Them!”
By Richie Allen | July 1, 2021
Robert Dingwall, a member of the JCVI (Joint Committee on Vaccination and Immunisation) has suggested that allowing children to catch Covid and build up natural immunity to the infection, may be safer than vaccinating them.
Dingwall (pictured) sits on the JCVI. The committee advises the government on who should get vaccinated and when. It is currently considering whether 12-18 year-olds should receive the jab. Dingwall took to Twitter yesterday and stated:
“Teenagers are at intrinsically low risk from Covid. Vaccines must be exceptionally safe to beat this. Given the low risk of Covid for most teenagers, it is not immoral to think that they may be better protected by natural immunity generated through infection than by asking them to take the possible risk of a vaccine.”
He went on to say that the pandemic, “would end through population immunity, whether from vaccination or prior infection”.
However, SAGE member John Edmunds told BBC Newsnight last night, that the country should not fully reopen until all secondary school children are vaccinated. He said:
“At some point we do have to dismantle all of these measures that we’ve put in place. I think, for me, the safest time to do that is when children have been vaccinated, certainly secondary-school-aged children at least. That’s the safest way.”
John Edmunds is a lunatic. As Robert Dingwall pointed out, Covid presents no real risk to children. Children should not be coerced into taking a medicine on behalf of someone else.
In fact, Dingwall should go further. The great majority of the population are at no serious risk from Covid. The evidence is overwhelming that the jabs present a far greater risk than the virus.
Government Says Vaccine Passports Won’t Be Mandatory – They’re Lying
By Richie Allen | June 30, 2021
The Daily Mail is reporting this morning that the government has shelved plans to use vaccine passports after July 19th, the so-called Freedom Day.
The Mail claims that it has been told that covid certification will not be required at mass gatherings when restrictions are lifted.
Government sources have revealed that those attending festivals, concerts or sporting events will not be required to show proof of vaccination or proof of immunity. That sounds good right?
Wrong. The Mail also reports that:
Organisers will, however, be permitted to run their own schemes, with the Premier League among those expected to introduce some form of certification to prove those attending football grounds do not pose a Covid risk.
There’s the kicker. Organisers will be permitted to run their own schemes. The government is simply passing the buck to the private sector. Here’s what I think will happen in the coming months. It’s all so predictable.
Shortly, the government will confirm that it will not be imposing mandatory covid certification. There will be lots of virtue signalling. Ministers will wax lyrical about civil liberties. “The UK is not that sort of country,” they will claim.
The government will say that it has listened to the hospitality industry and understands the concerns of pub and restaurant owners who do not want to be chasing customers for proof of vaccination.
From late July, through August and September, life will feel more normal. It’ll be a false dawn. We’ll hit October. Covid case numbers will rise steadily. Many of those who took the mRNA jabs will become seriously ill and die. This will be blamed on the mythical variants.
Testing will be ramped up. The redundant and thoroughly discredited PCR test will find Covid in nearly everyone who is screened. The government will say that there is a danger that the NHS will be overwhelmed. They’ll say that flu is back too. Of course it’ll be a very virulent strain of flu. The government will tell us that regretfully, restrictions must be reimposed.
There will be real panic in the hospitality and entertainment industries. Fearing for their businesses, owners will scream bloody murder. At the 11th hour a compromise will be reached. That compromise will be the introduction of vaccine passports.
Landlords and restaurateurs who were previously critical of the scheme, will rush to embrace it. People who had a covid booster jab and a flu jab (meaning they will have had four jabs in 2021), will demand the introduction of the passport to allow them to socialise.
Enormous pressure will be brought to bear on people like me who haven’t had a jab and never will. This was never about a virus. It was always about conditioning us to take gene altering vaccines and lots of them. It’s unimaginably evil, but it is happening.
American Medicine, American Malfeasance
By Dr. Gary Null and Richard Gale | Global Research | June 26, 2021
An issue that is rarely discussed or given serious attention is the over-specialization in healthcare. Modern medicine’s approach to identify and treat illnesses and tackle the reduction of infections has in many instances ceased to be multidisciplinary. Medicine has also become increasingly compartmentalized and confined to a rigid materialistic belief system that has now established its own set of standards, criteria and values that are often contrary to gold-standard scientific protocols. The consequence is that its narrow single-mindedness has insulated modern medicine from objective criticism and preserved its internal flaws, errors and fabrications, which have contributed to the unnecessary injury and death of countless patients.
US healthcare spending reached $3.8 trillion in 2019. Due to the Covid pandemic, expenditures for 2020 will be astronomically higher. One might expect that with the world’s most expensive healthcare system, the US would equally have the best evidence-based practices to keep its citizens healthy. By now we should be proficiently expert at preventing and reversing disease, while making minimal errors resulting in injury or death. However, the exact opposite is the case. Instead of minimizing disease-causing factors, American medicine causes more illness through misguided diagnostic testing, overuse of medical and surgical procedures, and over prescribing pharmaceutical drugs. The fundamental reason for this catastrophe is that today’s healthcare establishment, and corporate science in general, over relies on profit-generating motives.
Dr. Peter Gotzsche is arguably recognized as one of the world’s foremost experts in evaluating evidence-based medicine (EBM). As the co-founder of EBM’s preeminent flagship organization – the Cochrane Collaboration — to review and analyze peer-reviewed clinical research, he is intimately knowledgeable about the widespread corruption permeating the pharmaceutical industry and medical journals. In his book Deadly Medicines and Organized Crime, he writes,
“The reason why we take so many drugs is that drug companies do not sell drugs. They sell lies about drugs… The patients do not realize that although their doctors know a lot about diseases, human physiology and psychology, they know very little about the drugs that have been concocted and dressed up by the drug industry.”
After we take a fair and objective look at American medicine during the past five decades, especially at the statistics of iatrogenic fatalities, or deaths caused by prescribed medications and medical error, our healthcare establishment is found to be anything but benign. Despite its many noteworthy discoveries and merits, a substantial amount of recommended medical practice has failed patients. “If the medical system were a bank,” writes Dr. Stephen Persell at Northwestern University’s School of Medicine, “you wouldn’t deposit your money here, because there would be an error every one-in-two to one-in-three times you made a transaction.” Dr. Persell is referring to the rates of preventable medical errors causing patients serious injury and now the third leading cause of death.
There is excellent evidence to support the argument that iatrogenic deaths have passed cancer fatalities and are now challenging heart disease for the number one spot. A 2008 study found as many as half of adverse events reported by patients were not recorded in their hospital charts. As of 2017, investigations continue to find that less than 10% of medical errors are reported. Reported adverse effects vary depending on the specialty and frequently go unnoticed or are improperly evaluated. An additional study found that almost two thirds of cardiologists had refused to report a serious error they had direct personal knowledge of to an authority.
As one example, heart disease is America’s leading cause of fatality, accounting for 665,000 deaths annually. The CDC, which consistently undermines health threats if it means positioning itself in opposition to private commercial interests, estimates that 34 percent of cardiovascular fatalities are premature and preventable. In contrast, the American Heart Association claims 80 percent are preventable. What are the heads of our federal health agencies doing to advocate on the side of prevention? Little to nothing.
There is no realistic and science-based national policy in place to lessen cardiovascular, cancer and diabetic death rates. Since the most viable and effective means to prevent these diseases are natural and within every person’s means, it is not financially lucrative to divert federal funding away from pharmaceutical treatments and surgical procedures. The CDC and FDA are largely dependent upon monetary income received from the drug and medical device industries.
Earlier we reported about the systemic corruption and fraud that has plagued the CDC and FDA for decades. It would be far cheaper to completely empty, dismantle, fumigate and rebuild the agencies anew rather than continue exerting pressure for reforms, which have only perpetuated a killing spree by protecting life-threatening drugs, vaccines and unnecessary medical procedures. Dr. Gotzsche notes, the same is true for private drug companies. Despite the numerous lawsuits drug companies have lost in federal courts, nothing has fundamentally changed in order to deter them from illegal activities to increase profits. In fact, the cost of paying out settlements and settling lawsuits is factored into the expense of doing business.
A decade ago, we teamed up with three board-certified physicians to undertake the task to review the peer-reviewed literature in order to recalculate the statistics from many branches of medicine in order to arrive at a more realistic casualty rate due to medical error. We began with a basic question. Do the current standards of American medical practice and its supporting science prove that the recommended therapies and healthcare protocols – whether drugs, surgery, diagnostic methods, medical devices, etc – are actually effective? And if so, at what cost to the patients’ health and well-being?
Our results and final conclusions were startling and culminated in the release of a widely read and referenced book, Death by Medicine. We made every effort to avoid editorial commentary to our findings. We decided to only report the statistics and facts with our calculations. The fact that our data placed iatrogenic error as the number one cause of death in America was alone sufficient. What was novel in our analysis was that we included preventable deaths, such as certain infections and severe nutrient deficiency, which could have been easily corrected by clinicians and medical personnel if viable prevention programs had been part of our healthcare system. After publication the book was sent to hundreds of journalists, federal officials and non-profit medical organizations. It was completely ignored by the orthodoxy; however, it became increasingly popular among alternative and complementary medical physicians who were already fully aware of the structural dangers to public health within conventional medical care.
Revisiting American medicine’s legacy of iatrogenic deaths is now more crucial than ever because the same behaviors that have contributed to the nation’s leading cause of death are being repeated during the Covid-19 pandemic. The government and federal health officials are in reprehensible denial of inexpensive and highly effective drugs, such as Ivermectin and hydroxychloroquine, to treat early and middle stage SARS-2 infections. Cases of Covid infections and deaths have been grossly exaggerated. And now we are realizing that the efficacy and safety profiles of the vaccines are orchestrated scams. As a result, the entire institutional edifice to vaccinate the global population is destined to become the greatest scandal of the 21st century.
Unfortunately, nobody can acquire accurate statistics for Covid-19 vaccine associated injuries and deaths from the CDC’s Vaccine Adverse Events Reporting System (VAERS). Careful weekly monitoring of VAERS’ adverse event updates convince us that the entire system is criminally rigged. CDC officials overseeing the database are undoubtedly fudging numbers after ratio of adverse events, including deaths, per number of doses administered are compared to the more robust and accurate EudraVigilance database in the European Union and the less reliable Yellow Card System in the UK.
As of June 17, VAERS was reporting 329,021 injuries and 5,888 deaths due to the Covid vaccines. The database’s most recent update is reporting an additional 26,541 injuries but 1,972 less deaths. How can this sudden disappearance of almost 2,000 deaths be accounted for? The mysterious loss of fatality entries occurred during the same week as a CDC working group of outside medical professionals was reviewing an association between the mRNA vaccines and the rising number of reported cases of cardiac inflammation or myocarditis. The group concluded that there is indeed “a likely association.” The occasion of deleted deaths in VAERS is also on the heels of the Israeli Shamir Medical Center report that Pfizer’s vaccine is linked with occurrences of thrombotic thrombocytopenic purpura, an autoimmune disorder associated with a rare form of blood clotting. However, despite weekly local news stories around the nation about youth as young as 19 years of age dying of vaccine complications shortly after receipt of an mRNA vaccine, the CDC is claiming that all 1,200 persons, between 16-24 years of age, recovered and no deaths were reported. Does this account for the likely scrubbing of entries in VAERS?
But it is much worse. We only need to look at the European Union’s statistics for adverse Covid-19 vaccine events and compare that with VAERS and the CDC’s recent conclusion to realize there is a massive cover-up in our government’s efforts to sanitize the safety record of Covid vaccines. As of this week the EudraVigilance system is reporting over 1.5 million injuries and 15,472 deaths. Within those figures, 28,583 injuries and 1,862 deaths are from cardiac complications such as myocarditis.
Second, the EU and US have administered approximately the same number of Covid vaccine doses, roughly 409 million and 379 million respectively. Therefore we should expect to find a similar dose-to-injury ratio. Again we discover the CDC gaming the nation’s reporting system to lessen the perception of lethal risks. Based upon the EU ratio we can conservatively estimate that a minimum of 14,300 Americans have been killed by the vaccines so far. If we go back a week before the CDC scrubbed entries in VAERS, it would be over 17,000 Covid vaccine deaths. The actual number of Americans suffering adverse reactions would be 1.4 million.
In other words the EU is reporting 4 times more vaccine injuries and deaths than American health officials. In both the US and EU, Pfizer’s mRNA vaccine accounts for the majority of these casualties. Unless the Covid-19 vaccines engineer a personal vendetta against people holding EU passports, these numbers don’t add up.
Before the arrival of the Covid vaccines, Merck’s anti-inflammatory drug Vioxx was widely regarded as the single largest pharmaceutical catastrophe in American medical history. The drug should never have been approved and licensed in the first place; and, Merck knew beforehand that the drug would be lethal and concealed that documentation from FDA regulators. Vioxx was on the market for five years before being withdrawn. At the time of the federal class action lawsuit against Merck, FDA epidemiologist Dr. David Graham estimated the drug had killed 60,000 patients due to heart attacks and strokes. Since the majority of deaths were among elderly patients, a later report by the American Conservative predicted that upwards to half a million patients may have died from the drug over the course of a longer period. Yet during those years Merck was cashing in $2 billion annually from Vioxx sales, earning over double its eventual $4.8 billion fine after being found guilty.
To put this into a broader perspective, the Covid vaccines have only been distributed for six months and have now contributed to a realistic 17,000 deaths or upwards towards 30,000 this year alone. Since the vaccines’ immunity quickly wanes and it seems certain they provide little protection against new SARS-2 strains, health officials are already recommending regular booster shots. Similar to a prescription medication, those who buy into the vaccine propaganda hype are in principle relying upon these vaccines for life or until such time the virus resides into just a seasonal nuisance. Consequently iatrogenic vaccine injuries and deaths may likely continue at current rates during forthcoming years. The Covid-19 vaccines are on track to outpace the conservative number of Vioxx deaths over three-fold and even modern medicine’s most deadly drugCerivastatin, manufactured by Bayer in the late 1990s and responsible for over 100,000 deaths during the four-year period it was on the market. In short time, Covid vaccines will be the deadliest drug to have emerged from Big Pharma.
A study published in the Journal of Patient Safety estimated that 400,000 unnecessary and preventable deaths occur annually in American hospitals alone. At that rate, it is not surprising that the large majority of deaths ruled as SARS-2 infections happened in hospitals. If our federal health officials had been competent, and less compromised by the demands and influence of drug makers, most of these fatalities likely would never have occurred.
It has been estimated that US taxpayers have paid out $39 billion for Covid-19 vaccine development, funding and towards nationalized response measures. Most of this has been horribly wasted after we consider other options on hand to curb the pandemic but were categorically ignored. “In the case of vaccines in general,” the journal Health Affairs observed,
“the government often plays an outsized role, but in the era of Covid-19 the government’s role was even more central than usual. The government essentially removed the bulk of traditional industry risks related to vaccine development: a) scientific failures, b) failures to demonstrate safety and efficacy, c) manufacturing risks, and d) market risks related to low demand.”
While this may shock and disturb a rational person, Health Affairs – a thoroughly orthodox medical publication – applauds the government’s negligent measures as “money well spent.”
For this reason it is crucial to understand the terrible decisions made during the Covid pandemic in the context of modern medicine’s past crimes and preventable failures. In the coming months Anthony Fauci’s reputation will become further tainted. We might predict he will resign as more evidence of incompetence emerges, and, in our opinion, perhaps criminal negligence in his handling of the pandemic and efforts to whitewash the US’s role in supporting gain of function research leading to the genetic engineering of the SARS-2 virus. Fortunately, unlike past scandals when misguided medical decisions were responsible for thousands of unnecessary disabilities and deaths, numerous doctors and scientists worldwide are raising their voices to condemn the lethal policies of the CDC, NIAID, British Health Ministry and the World Health Organization.
So what can we reasonably surmise at this point? At one time most Americans trusted science, medicine and our healthcare system without question or criticism. However, today we observe systemic corruption and gross conflicts of interest across the same federal health agencies that have also contributed to untold medical errors and deaths prior to SARS-2 arrival. They have weaponized pharmaceutical science and a supplicant braying media supports this perversion of medical facts. Now the drug-happy media is attacking the truth-tellers, the physicians, professors and accomplished journalists who are risking their careers and reputations to bring forth the fallacies in the pandemic narrative. This is one battle that the silent majority can find its voice and courage to step forth and support.
Richard Gale and Gary Null PhD direct Progressive Radio Network.
Hypocritical Gospel according to the Covidians
By Elephant City | The Conservative Woman | June 28, 2021
THE recent spectacle of the G7 leaders in Cornwall posing for photos in masks and then ripping them off to party down with no social distancing is only the latest and most blatant example of double standards from the Covidians. For anyone paying attention, they have been giving us a daily masterclass in advanced hypocrisy.
The Covidian faith is strongest among Left-leaning elite managerial types. Safetyism is a huge part of their religion. These are people who slather sunblock on their kids before they step out the door and monitor them with tracking apps on their phones. And then they allow their kids to be shot up with an experimental ‘vaccine’ (gene therapy) that was tested on only 1,131 children who were followed up for less than six months.
The Covidians tremble in their homes like gutless cowards because of a disease that has an average survival rate of at 99.8 per cent for the general population and nearly 100 per cent for the healthy population. And then they allow themselves to be injected with an experimental gene therapy with less than a year of safety data, authorised by regulatory agencies fully corrupted by Big Pharma money. So much for ‘stay safe’!
Covidianism is a branch of wokism. The woke take every opportunity to manufacture status by loudly proclaiming their concern for ‘social justice’. They seized on the pandemic as a chance to flaunt their shining virtue to the world by hanging out of windows and lustily banging pots and clapping. They conveniently ignored the fact that the lockdown policies they so eagerly supported crushed the working class. They considered it completely natural that a class of workers should have to deliver their food, work in the grocery stores, take their garbage and clean their streets, while they hid behind their computer screens and called for ever harsher lockdowns. Their idea of social justice consists of forcing others to face the risks of Covid while they attend Zoom meetings in their sweatpants.
As card-carrying members of the woke, the Covidians surely spent the last four or five years eagerly mouthing the central tenet of the faith: that the ‘patriarchy’ is the root of all evil; that a gang of Western white men has spent the last few centuries brutally oppressing everyone else in the world. And then, without any irony, they slavishly follow every command of Western white men such as Boris Johnson, Chris Whitty, Matt Hancock, Anthony Fauci and Joe Biden.
Likewise, as good wokesters, they no doubt eagerly signed up to the campaign to ‘defund STEM’ (because science itself is a tool of the dreaded patriarchy). Now, without the slightest tinge of shame, they angrily insist that we must ‘follow The Science.’ Of course, what they mean by ‘The Science’ is the institutional narrative favourable to Big Pharma.
The Covidians profess tremendous faith in the vaccine. Yet they find it almost impossible to let go of their precious masks, their flag of tribal identity. Likewise, despite their faith in the vaccine, the Covidian faithful insist that everyone else on earth be forced to take the vaccine (though presumably, if the vaccine works, they are protected so it doesn’t matter whether others take it).
As members of the elite managerial class, they obsess about the quality of their food, scrutinising food labels to be sure that anything they put into their bodies is organic, artisanal and free from chemicals. And then they queue to have a syringe full of unknown, barely tested, industrial genetic products shot directly into their bloodstream.
No doubt most Covidian women are strident feminists who mouth the slogan ‘my body, my choice’. Yet they eagerly support a national campaign of coerced ‘consent’ wherein the state forces the people to accept injection of unknown and potentially dangerous genetic material into their bodies. They are supporting the penetration of the state into their physical beings – mechanical rape on an industrial scale.
Likewise, these feminists have no doubt spent the last few decades working their way into every boardroom, professorship and political office. Now they vocally support being locked in their homes by the state. They gladly accept limits on their freedom that would make Saudi Arabian women look like liberated hippie chicks.
The Covidians claim that black lives matter, and yet they support policies that damage the working class, in which people of colour are disproportionately represented. Likewise, they support the regime that actively suppresses knowledge and use of ivermectin, a drug that would eliminate Covid. Thus they perpetuate a pandemic that disproportionately affects people of colour.
If you look closely at the words and actions of the Covidians, you will see nothing but contradiction and hypocrisy. This indicates an appalling lack of principles, because principles would demand some consistency across words and actions. Rather, for the Covidians, it’s all about obedience to the diktats of the mainstream media and government agencies. These people are reeds bending in the wind, incapable of thinking for themselves and only concerned with appearing virtuous. They have stood for nothing and fallen for everything.
These are just a few examples: please add more in the comments section. We have a duty to history to document the full depths of the mind-boggling hypocrisy of the Covidians.
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A low-fat, high-carb diet has been the largest public health experiment in history. It’s past time for a rethink.
By Malcolm Kendrick | RT | November 25, 2020
New research suggests that four billion people globally will be overweight in 2050. This trend can be traced back to the ‘low-fat, high-carb’ guidelines first issued in the 70s, and should prompt a major U-turn on dietary advice.
A recent report from the Potsdam Institute predicts that by 2050 there will be four billion overweight people in the world, with one-and-a-half billion of them obese. This is not entirely surprising. The world has been getting fatter for years, and things do not seem to be slowing down.
Why is this happening? … continue
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