Lawmakers demand answers on Facebook censorship at behest of Biden administration
By Cindy Harper | Reclaim the Net | June 10, 2021
Following the revelation that Facebook’s CEO Mark Zuckerberg was in email communication with the country’s top epidemiologist Dr. Anthony Fauci, House Republicans sent a letter demanding answers on why the company censored lab leak theories.
According to the Republican legislators, the emails suggest that Fauci advised Facebook to censor the lab leak theories.
Ranking members of the House Judiciary Committee and House Oversight Committee, Jim Jordan and James Comer wrote a letter addressed to Zuckerberg demanding answers on why his company censored content suggesting COVID-19 leaked from a lab.

The letter accuses the government of using a private company to violate free speech. It requested Facebook to provide all documents and communication between its employees and government officials.
“In light of Facebook’s subsequent censorship of certain COVID-19 content – including content about the pandemic’s origin – these communications with Dr Fauci raise the prospect that the federal government induced Facebook to censor certain free speech in violation of the First Amendment,” the letter states.
“Facebook’s censorship decisions did not occur in a vacuum, and there are indications that Facebook may have made content-moderation decisions regarding COVID-19 at the behest of certain government policies and positions,” the legislators added.
Until recently, most scientists dismissed the idea that the virus leaked from a lab in China. However, in recent weeks, evidence supporting the lab leak theory has emerged, forcing Facebook to review its COVID-19 misinformation policies.
In late May, after President Joe Biden announced that the lab leak theory needed more investigation, Facebook announced it would no longer flag content suggesting that COVID 19 was man-made.
The legislators gave Facebook two weeks to respond to the letter.
Canada becoming an actual death camp
By Jon Rappoport | No More Fake News | June 10, 2021
They’re called the College of Physicians and Surgeons of Ontario (CPSO).
As their home page states, they “regulate the practice of medicine in Ontario. Physicians are required to be members to practice medicine in Ontario.”
In other words, CPSO is THE medical board. They run the show. If practicing doctors make a wrong move or say the wrong thing, CPSO is there to step on their faces and discipline them and even cancel their licenses to practice.
But now a new rebel group of Canadian MDs has emerged. Why? Because CPSO has issued a fascist edict threatening practicing doctors. Read the threat carefully.
College of Physicians and Surgeons of Ontario [CPSO] Statement on Public Health Misinformation (4/30/21):
“The College is aware and concerned about the increase of misinformation circulating on social media and other platforms regarding physicians who are publicly contradicting public health orders and recommendations. Physicians hold a unique position of trust with the public and have a professional responsibility to not communicate anti-vaccine, anti-masking, anti-distancing and anti-lockdown statements and/or promoting unsupported, unproven treatments for COVID-19. Physicians must not make comments or provide advice that encourages the public to act contrary to public health orders and recommendations. Physicians who put the public at risk may face an investigation by the CPSO and disciplinary action, when warranted. When offering opinions, physicians must be guided by the law, regulatory standards, and the code of ethics and professional conduct. The information shared must not be misleading or deceptive and must be supported by available evidence and science.”
WE’RE YOUR BOSSES. YOU DO WHAT WE TELL YOU TO DO. SHUT YOUR MOUTHS. MARCH STRAIGHT AHEAD. KILL YOUR PATIENTS IF YOU HAVE TO, BUT OBEY US.
The new rebels against this monster call themselves the Canadian Physicians for Science and Truth. This is a brief excerpt from their response:
“On April 30, 2021, Ontario’s physician licensing body, the College of Physicians and Surgeons of Ontario (CPSO), issued a statement forbidding physicians from questioning or debating any or all of the official measures imposed in response to COVID-19.”
“We regard this recent statement of the CPSO to be unethical, anti-science and deeply disturbing.”
“As physicians, our primary duty of care is not to the CPSO or any other authority, but to our patients.”
“The CPSO statement orders us to violate our duty and pledge to our patients…”
I wondered what medical treatments, in general, CPSO supports and tolerates. It took me three minutes to find a Toronto outfit called the Centre for Addiction and Mental Health Foundation (CAMH). They promote electro-convulsive therapy. In other words, shock treatment.
In other words, delivering electric shocks to the brain. As a cure for “mental illness.” I call it torture.
Apparently, this treatment is just fine and dandy, but telling patients the COVID lockdowns are criminal is forbidden by the Nazi bureaucrats at CPSO. Saying the vaccine is dangerous is forbidden. Saying masks are useless and harmful is forbidden.
What would happen if these medical rebels, the Canadian Physicians for Science and Truth—say, 10,000 of them—took this war to the wall?
Practiced non-harmful medicine, kept warning their patients about the sociopathic COVID regulations and the vaccine, refused to knuckle under to the Nazi bureaucrats, even to the point of having their licenses stripped and going to jail?
What would happen, as many thousands/millions of Canadians rallied to their side?
I’ll tell you what would happen. Sanity. Revolution. The downfall of the scum.
We’re at Nuremberg 2.0, people. If you don’t know what that means, look it up.
Doctors clear their vision and their brains and do their level best to HEAL, or they follow orders of the Commandants and maim and kill. It’s one side or the other.
In my 83 years, I’ve known a few very good doctors, and a number of The Cold Ones. The Cold Ones administer, without feeling or remorse, the Book of Death.
They’re ice on the outside, and rotting fungus and stench within.
Many of them sit at the top of medical boards.
They turn open societies into concentration camps.
REBEL.
Kentucky Judge Invalidates All of Governor Bashear’s State of Emergency Actions
By John H. Bryan | The Civil Rights Lawyer | June 8, 2021
Today my colleague from Kentucky, Chris Wiest, received an awesome ruling from the Circuit Court of Boone County declaring that all of Governor Andy Bashear’s emergency orders and actions are unconstitutional and void. The ruling was in the state-court challenge to the governor’s emergency powers executive orders, filed by Wiest on behalf of Beans Cafe’ & Bakery.
Dr. Stephen Petty, an actual expert in masks, testified at the trial about their uselessness under the circumstances in which they’re being idolized. Here’s an excerpt from the order pertaining to Dr. Petty. For those bureaucrats and social media tyrants who would censor this, this is from an actual court order issued today. Not that you care:
Stephen E. Petty, P.E., CIH, testified as an expert and was accepted as such without objection. Mr. Petty has served as an expert witness in approximately 400 cases relating to toxic or infectious exposure, personal protective equipment (“PPE”), and as a warning expert. He also served as an epidemiology expert for the plaintiffs in the Monsanto “Roundup” cases, and for those in the Dupont C8 litigation. In connection with his service as an expert, he was deposed nearly 100 times and has provided court testimony in approximately 20 trials. Mr. Petty holds nine U.S. patents, has written a book comprising nearly 1,000 pages on forensics engineering, is a certified industrial hygienist, and a recognized expert with the Occupational Safety and Health Agency. Mr. Petty helped write the rules on risk assessment for the State of Ohio and has trained Ohio’s risk assessors.
Mr. Petty explained that the field of his expertise is “to anticipate and recognize and control things that could hurt people, everything from making them sick to killing them.” He testified that, in this context, he has analyzed the use of masks and social distancing in connection with Covid-19. He testified that both the six-foot-distancing rule, and mask mandates, are wholly ineffective at reducing the spread of this virus. Masks are worthless, he explained, because they are not capable of filtering anything as small as Covid-19 aerosols. In addition, masks are not respirators and lack the limited protections that respirators can provide.
The N-95 respirator, which he states is in the bottom class of what may be classified as a respirator, is rated to filter 95% of all particles that are larger than .3 microns. However, a Covid-19 particle, which is only between .09 to .12 micron, is much smaller. Mr. Petty further explained that an N-95 will not even filter above .3 microns if it is not used in accordance with industry standards. Among the requirements, respirators must be properly fitted to seal along the face, and they also must be timely replaced. Mr. Petty stated that N-95 masks, which he said are often utilized as surgical masks, are “not intended to keep infectious disease from either the surgeon or from the patient infecting each other” but only to catch the “big droplets” from the surgeon’s mouth.”
According to Mr. Petty, masks have no standards, are not respirators, and do not even qualify as protective equipment. In contrast, respirators have standards, including rules that state respirators may not be worn by persons with facial hair, must be fitted to ensure a seal, and must be timely replaced—or, as in higher end respirators, the cartridges must be replaced to prevent saturation. In addition, standards for respirators also require users to obtain a medical clearance because the breathing restriction can impair lung function or cause other problems for persons having such limitations. Putting those persons in a respirator can harm their well-being.
Concerning the effectiveness of respirators, Mr. Petty explained that it comes down to “big stuff” versus “small stuff.” Big stuff can be taken out by the body’s defenses, such as its mucus tissue, where droplets can be caught and eliminated. The small stuff, however—like aerosols—are more dangerous. Masks cannot filter the small stuff. According to Petty, because Covid-19 particles are comprised of aerosols, it is really, really, small stuff. And, as he pointed out, an N-95 is designed to filter larger particles. Even for particles as large as .3 micron, Mr. Petty testified that an N-95’s effectiveness is in direct proportion to its seal. In fact, he stated it becomes completely ineffective if 3% or more of the contact area with the face is not sealed.
Mr. Petty testified that masks leak, do not filter out the small stuff, cannot be sealed, are commonly worn by persons with facial hair, and may be contaminated due to repetitive use and the manner of use. He emphatically stated that mask wearing provides no benefit whatsoever, either to the wearer or others.
He explained that the big droplets fall to the ground right away, the smaller droplets will float longer, and aerosols will remain suspended for days or longer if the air is stirred. Mr. Petty testified that the duration of time that particles remain suspended can be determined using “Stoke’s Law.” Based on it, for particles the size of Covid-19 (.12 to .09 micron) to fall five feet would take between 5 and 58 days in still air. Thus, particles are suspended in the air even from previous days. And so, he asks, “If it takes days for the particles to fall, how in the world does a six-foot rule have any meaning?”
Mr. Petty acknowledged that both OSHA and CDC have recommended that people wear masks. However, he called this “at best dishonest.”61 As an example on this, he pointed to CDC guidance documents where, on page 1, it recommends wearing a mask; but then on page 6, admits that “masks, do not provide . . . a reliable level of protection from . . . smaller airborne particles.”62 According to Mr. Petty, those agencies have smart individuals who know better. Mr. Petty points out that, even before March 2020, it was known that Covid-19 particles are tiny aerosols. And on this, he states that he insisted that fact early on. He also points to a more recent letter by numerous medical researchers, physicians and experts with Ph.D.s, asking the CDC to address the implications of Covid-19 aerosols. During Dr. Stack’s subsequent testimony, he also acknowledged that Covid-19 is spread “by . . . airborne transmission that could be aerosols . . . .”
Finally, Mr. Petty pointed to another recent study by Ben Sheldon of Stanford University out of Palo Alto. According to that study, “both the medical and non-medical face masks are ineffective to block human-to-human transmission of viral and infectious diseases, such as SARS, CoV-2 and COVID-19.”64 The Court finds the opinions expressed by Mr. Petty firmly established in logic. The inescapable conclusion from his testimony is that ordering masks to stop Covid-19 is like putting up chain-link fencing to keep out mosquitos. The six-foot- distancing requirements fare no better.
The judge summarizes the situation nicely:
It is obvious from even a cursory review that the orders issued over the past fifteen months “attempt to control” and seek “to form and determine future rights and duties” of Kentucky citizens. These included ordering the closure of all businesses, except those the Governor deemed essential. He ordered churches closed, prohibited social gatherings, including at weddings and funerals, prohibited travel, and through CHFS, even prohibited citizens from receiving scheduled surgeries and access to medical care. And then there is the order that everyone wear a mask. These are, undeniably, attempts to control, set policy, and determine rights and duties of the citizenry. Except in those instances where the federal courts have stepped in, Defendants assert authority to modify or re-impose these orders at their sole discretion. Consider, for example, the recent modification of the mask mandate. It orders persons who did not get vaccinated for Covid-19 to wear masks but lifts that requirement for others. That is setting policy and determining future rights and duties.
At the hearing, Defendants took exception to the Attorney General’s characterization of the Governor’s actions as a “lockdown,” and argued that prohibiting persons from entering those restaurants is not the same as ordering that they be closed. But that doesn’t minimize the impact on those who lost their businesses as a result, or those in nursing homes condemned to spend their final hours alone, deprived of the comfort from loved ones (or even any real contact with humanity), or those citizens who the Governor prohibited from celebrating their wedding day with more than ten persons, or those he forced to bury their dead alone, without the consoling presence of family and friends (and who likewise were deprived of paying their final respects), or those persons who were barred from entering church to worship Almighty God during Holy Week, and even Easter Sunday, or those persons who were denied access to health care, including cancer-screenings, or those denied entry into government buildings (which they pay for with their taxes) in order to obtain a necessary license, and who were forced to wait outside for hours in the sweltering heat, or rain, purportedly to keep them from getting sick.
What the people have endured over the past fifteen months—to borrow a phrase from United States District Judge Justin R. Walker—“is something this Court never expected to see outside the pages of a dystopian novel.” Yet, Defendants contend that the Governor’s rule by mere emergency decree must continue indefinitely, and independent of legislative limits. In effect, Defendants seek declaratory judgment that the Constitution provides this broad power so long as he utters the word, “emergency.” It does not. For this Court to accept Defendant’s position would not be honoring its oath to support the Constitution; it would be tantamount to a coup d’état against it.
Here’s the order itself:
Yes, life is now a dystopian novel. Let’s hope this patriot judge’s order stands up on appeal in the state appellate courts in Kentucky. And thanks to Chris Wiest and the AG of Kentucky for fighting the good fight. The order notes that the permanent injunction against the governor goes into effect on June 10, 2021 at 5:00 p.m.
New Study Shows Hydroxychloroquine Boosts Covid Survival By More Than 200%
By Richie Allen | June 10, 2021
US scientists have claimed that a malaria drug can increase the survival rate of patients with severe Covid-19 by as much as 200 per cent. Doctors found that when ventilated patients were given hydroxychloroquine with zinc, their condition improved rapidly.
The study was conducted by Saint Barnabas Medical Center in New Jersey. 255 patients were involved. The results were published two weeks ago here.
Friends and supporters of former US President Donald trump were quick to jump on the findings. Trump was a strong advocate for treating severe Covid-19 with hydroxychloroquine.
Trump was widely criticised for pushing the drug. Scientists labelled him reckless. His adviser Dr. Anthony Fauci said at the time, that all the evidence to hand suggested that the treatment was ineffective against covid.
In March this year, the World Health Organization warned against using the drug to treat coronavirus. The WHO produced data which alleged hydroxychloroquine was ineffective.
Yet the authors of the new report claim:
“We found that when the cumulative doses of two drugs, HCQ and AZM, were above a certain level, patients had a survival rate 2.9 times the other patients.”
Last December, a study published by the International Journal of Antimicrobial Agents showed 84 per cent fewer hospitalizations among patients treated with the drug.
In January this year, a study carried out by Hackensack Meridian Health, showed encouraging results in patients with mild covid symptoms who were given hydroxychloroquine.
As I write this, UK Health Secretary Matt Hancock is facing a committee in Westminster. He’s answering questions about his government’s handling of the pandemic. It’s a walk in the park for Hancock. It’s one softball question after another so far.
Don’t hold your breath waiting for a committee member to ask him if he’d considered sending hydroxychloroquine or ivermectin to care homes and hospitals, to treat those who had to be ventilated for severe covid.
WHO’s Chief Scientist Served with Legal Notice for Disinformation and Suppression of Evidence
By Colin Todhunter | OffGuardian | June 9, 2021
On 25 May 2021, the Indian Bar Association (IBA) served a 51-page legal notice on Dr Soumya Swaminathan, the Chief Scientist at the World Health Organisation (WHO), for:
[H]er act of spreading disinformation and misguiding the people of India, in order to fulfil her agenda.”
The Mumbai-based IBA is an association of lawyers who strive to bring transparency and accountability to the Indian justice system. It is actively involved in the dissemination of legal knowledge and provides guidance and support to advocates and ordinary people in their fight for justice.
The legal notice says Dr Swaminathan has been:
Running a disinformation campaign against Ivermectin by deliberate suppression of effectiveness of drug Ivermectin as prophylaxis and for treatment of COVID-19, despite the existence of large amounts of clinical data compiled and presented by esteemed, highly qualified, experienced medical doctors and scientists,”
And:
Issuing statements in social media and mainstream media, thereby influencing the public against the use of Ivermectin and attacking the credibility of acclaimed bodies/institutes like ICMR and AIIMS, Delhi, which have included ‘Ivermectin’ in the ‘National Guidelines for COVID-19 management’.”
The IBA states that legal action is being taken against Dr Swaminathan in order to stop her from causing further damage to the lives of citizens of India.

Dr Soumya Swaminathan, WHO Chief Scientist
The notice is based on the research and clinical trials carried out by the ‘Front Line COVID-19 Critical Care Alliance’ (FLCCC) and the British Ivermectin Recommendation Development (BIRD) Panel. These organisations have presented an enormous amount of data that strengthen the case for recommending Ivermectin for the prevention and treatment of COVID-19.
The IBA says that Dr Swaminathan has ignored these studies and reports and has deliberately suppressed the data regarding the effectiveness of Ivermectin, with an intent to dissuade the people of India from using it.
However, two key medical bodies, the Indian Council for Medical Research (ICMR) and the All India Institute of Medical Sciences (AIIMS) Delhi, have refused to accept her stand and have retained the recommendation for Ivermectin, under a ‘May Do’ category, for patients with mild symptoms and those in home isolation, as stated in ‘The National Guidelines for COVID-19 management’.
It is interesting to note that the content of several web links to news articles and reports included in the notice served upon Dr Swaminathan, which was visible before issuing the notice, has either been removed or deleted.
It seems that the vaccine manufacturers and many governments are desperate to protect their pro-vaccine agenda and will attempt to censor information and news regarding the efficacy of Ivermectin.
The legal notice can be read in full on the website of the India Bar Association.
Is there a Problem with the Lopez-Medina, Colombia-based Study Implicating Ivermectin?
Major Pharma Companies Including Merck Funding the Trial Site during the Study
By Michael B. Goodkin MD, FACC | TrialSite News | June 9, 2021
Although a great majority of ivermectin-based studies have indicated real promise, one particular study conducted by a small trial site in Colombia received unprecedented media attention when the study results indicated negligible impact. What hasn’t been disclosed by media is the seriously questionable pharmaceutical industry support of this one trial site. During the study, a handful of some of the largest drug companies in the world gave this site money. What’s not clear is why this occurred and whether the funds are correlated to some nefarious agenda. This author suggests that the publisher should have scrutinized this industry funding perhaps more carefully.
On March 4th, 2021, an article appeared in JAMA titled, “Effect of Ivermectin On Time To Resolution of Symptoms Among Adults With Mild COVID.” It concluded, “The findings do not support the use of ivermectin for treatment of mild COVID-19, although larger trials may be needed to understand the effects of ivermectin on other clinically relevant outcomes.”
Dr. Eduardo Lopez-Medina et al. from Cali, Colombia, randomized 400 mildly ill patients, averaging 37 years old, to ivermectin 0.3 mg/kg or placebo. The time to resolution for ivermectin-treated patients was 10 days and placebo patients 12 days, which was not statistically significant.
Much has been written about the methodologic problems of the study but few read to the bottom of the article to see this:
Conflict of Interest Disclosures: Dr. López-Medina reported receiving grants from Sanofi Pasteur, GlaxoSmithKline, and Janssen as well as personal fees from Sanofi Pasteur during the conduct of the study. Dr. Oñate reported receiving grants from Janssen and personal fees from Merck Sharp & Dohme and Gilead outside the submitted work. Dr. Torres reported receiving nonfinancial support from Tecnoquímicas unrelated to this project during the conduct of the study. No other disclosures were reported.
Considerable press outlets noted this study, we suspect due to the fact that the ivermectin results were negligible, but none of the media addressed the possibility of conflict with industry.
Absolutely nothing has been written about the fact that the study was sponsored by Centro de Estudios en Infectogía Pediatrica and the authors were paid by 3 drug companies making COVID vaccines–Sanofi Pasteur, GlaxoSmithKline, and Janssen– and two making COVID therapeutics–Gilead and Merck.
We have some questions about this. Why did the authors disclose that they were receiving industry sponsor funds during the conduct of the study? Were these funds to actually direct the ivermectin study? That would most certainly be a conflict of interest material.
Merck’s expressed their intent on competing against the ivermectin generic approach. Why would this company be funding this small trial site operation in Colombia?
How could JAMA even think about publishing an article sponsored by 5 drug companies centering on a study targeting a generic competitor? Any layperson seeing this could think that this was highly suspect.
The potential conflict of interest was so severe that no journal should have published it.
Why would anyone do this study?
Was there a pressing need to know if 37-year-old patients got better sooner with ivermectin than placebo? There were a lot of resources put into this study. The only possible reason to do the study was for drug companies to have a vehicle to publish negative data about ivermectin. Is there anyone who believes the study was sponsored to add to the scientific knowledge about ivermectin for the treatment of COVID?
On February 4th, 2021, Merck, who had the original patent on ivermectin, put out a statement regarding ivermectin for COVID:
• No scientific basis for a potential therapeutic effect against COVID-19 from pre-clinical studies;
• No meaningful evidence for clinical activity or clinical efficacy in patients with COVID-19 disease; and
• A concerning lack of safety data in the majority of studies.
If Merck believed these statements to be true, why would they feel the need to go public with them?
Merck’s vaccine had failed. Merck had bought a company, Oncoimmune, for $425 million and gotten $356 million from HHS in taxpayer money to develop a therapeutic agent, CD24c. They had a material conflict of interest. Later, the European Medicines Agency and World Health Organization both quoted Merck’s statement while ignoring the conflict of interest and science in recommending against the use of ivermectin for COVID, other than for research. Were they influenced by Merck? CD24c was dropped, and Merck has oral antiviral molnupiravir in a phase II-III trial. Why would Merck sponsor a trial of ivermectin?
Why would JAMA publish an article showing that young patients who are expected to recover quickly don’t get better much more quickly with ivermectin?
This article did not warrant publication in JAMA. The only possible reason to publish it was to present false, negative information about ivermectin to readers.
Why was the age of the patients not mentioned in the key findings or conclusions?
The age of the patients made the article irrelevant. It could not have been an accident that the age was not mentioned in the key findings and conclusions. That would never happen at JAMA. The authors anticipated that many readers would miss the age of the patients and conclude that ivermectin is ineffective in early COVID. Dr. Adfarsh Bhimraj at Cleveland Clinic who heads the committee writing COVID recommendations for the Infectious Disease Association of America spoke with Helio Medical News on ivermectin. He had a similar observation in the Washington Post.
“This was a well-done, but small trial in patients with mild or moderate disease,” Bhimraj said. He suggested that this is a negative study for a non-mortality outcome, but because the numbers were small, it might not have produced a statistically significant difference in effect size. The evidence is not enough to warrant a recommendation for the use of ivermectin. Other US experts who commented on the article have failed to notice the age of the patients and drug company sponsorship. It has crossed few American physicians’ minds that JAMA could be corrupted and knowingly publish a study with deceptive results in order to help drug companies.
Was the data fraudulent?
If the purpose of the article was to make it appear that ivermectin was ineffective in mild COVID, there is no reason to believe the data was real. There is no published randomized data for comparison. In the Dominican Republic, Dr. Jose Natalio Redondo reported that in 1300 patients with all degrees of illness, the length of illness went from 21 days to 10 days with ivermectin treatment.
Was JAMA aware that there was concern they had been corrupted and the article unreliable?
Sixteen members of the AMA Board of Directors were emailed that it appeared that JAMA had been infiltrated and the article fraudulent on March 10th, 2021. Eleven JAMA editorial board members were emailed about it April 12th. And one was spoken to. The same email was sent to executive editor Dr. Phil Fontanarosa April 13th. This reply was sent:
“Your message was brought to my attention.
I will look into these issues as outlined in your letter.
Please bear with me, as this will take some time, given the number of issues and the complexity of the concerns you raise, as well as other urgent issues and priorities we are addressing right now.”
As of 6/8/21, the article has been read online 759,000 times. How many of those readers concluded that ivermectin is ineffective for mild COVID and, as a result, did not prescribe it for their patients? To put things in perspective, Uttar Pradesh, India, with 210 million people, started ivermectin in August. By December, their mortality rate was 0.26 per 100,000. In the US, in December, it was 11 times higher at 2.8 per 100,000. Admissions in Mexico are down 75% due to ivermectin.
The JAMA article of 3/4/21 was a cleverly devised drug company creation designed to create the false impression that ivermectin was ineffective in mild COVID by claiming it didn’t shorten the duration of illness significantly. They knew people would miss the age of the patients and not read to the bottom of the article to see that it was sponsored by 5 drug company competitors. They knew people would leap to the conclusion that ivermectin was completely ineffective for COVID, not realizing that the article could not address its effects on hospitalization and death. An infectious disease doctor friend sent it to me as proof that ivermectin does not work. Drug companies would not have gone to these lengths if they did not fear ivermectin as a competitor.
JAMA reviewers could not possibly have missed the obvious conflict of interest. It was obviously their intention to spread misinformation. Leaving out the age of the patients was intentional to make readers think it was ineffective in everyone. The article has not only led to patient care being adversely affected but the article has been widely quoted as evidence against the use of ivermectin. WHO says it is the number one article in support of its position.
Doctors should contact JAMA to understand what is going on with the investigation. JAMA should report on their findings as they committed to this author to undertake an investigation.
Is this why the MSM don’t mention Sweden any more?
By Kathy Gyngell | The Conservative Woman | June 8, 2021
WHATEVER happened in Sweden with its policy of no masks and no lockdowns ?
In his latest brilliant video, Ivor Cummins invites us to see. Succinct and logical as ever, it is another must-watch. After making a statement about the official and therefore uncensorable data his analysis draws on – all the links to his evidence are provided – he asks the simple question: Who got the science correct? Ferguson and his big outfit at Imperial College, massively funded by Gates and Big Pharma interests? Or Anders Tegnell, Sweden’s chief epidemiologist, who said he could be judged around this time in 2021? The answer is Sweden, which followed the World Health Organisation’s 2019 pandemic guidelines that Britain threw in the bin.
Cummins goes on to show the real-world risk of death from Covid to be extremely small for those with PCR positive tests and infinitesimal for the rest. Taking Ireland as an example, he shows there is no evidence of excess deaths for the year 2020 and that Covid deaths simply make up a chunk of the normal deaths that would be expected anyway.
You can watch the video here.
The source article for the Sweden Data: https://shahar-26393.medium.com/not-a…



