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NYC Mayor Eric Adams says online platforms need to use AI to censor

By Cindy Harper | Reclaim The Net | May 22, 2022

New York City Mayor Eric Adams has used this month’s Buffalo shooting to call for more social media censorship.

Speaking live on PIX11’s Morning Show, Adams was asked by the host Hazel Sanchez what could be done about regulating social media.

“Governor Hochul, she was on PIX11, demanding social media platforms be held accountable. Now, you’ve been calling for that since the suspected Brooklyn subway shooter, Frank James, allegedly posted racist rants online,” Sanchez said. “But social media’s been around and unregulated for a long time. So what kind of change can you see happening?”

Mayor Adams responded, saying that it was time for social media platforms to start using “artificial intelligence to identify words, identify phrases, to immediately remove and censor some of this information.”

Mayor Adams likened the censorship techniques to the removal of President Trump’s Twitter account; “We did it to Donald Trump on Twitter. He was dangerous to the country. So why aren’t we doing it to the everyday people who are using it and is dangerous to our neighborhoods and communities?”

Likening his censorship demands to his similar demands for social media platforms to censor some forms of rap on social media, Adams stated, “The type of violence that’s being promoted on social media is beyond anything I’ve ever witnessed before.

“Particularly in some of the drill music that actually taunts and threaten people. There’s a direct correlation. That’s the type of social media monitoring we believe the social media companies should do.”

Earlier this year, New York City Mayor Eric Adams expressed concern about drill rap, a form of trap music popular in the city, because of its depiction of violence and firearms. Drill artists and rap writers have expressed concerns over the mayor’s remarks.

“We pulled Trump off Twitter because of what he was spewing,” Adams, a former NYPD officer, said at the time. “Yet we are allowing music, displaying of guns, violence, we’re allowing it to stay on these sites.”

“We are going to pull together the social media companies, and state that you have a civic and corporate responsibility.”

May 22, 2022 Posted by | Civil Liberties, Full Spectrum Dominance | | 1 Comment

Bill Gates’ media control dream

By Keean Bexte | The Counter Signal | May 19, 2022

The Bill and Melinda Gates Foundation has doled out over $319 million in grants, awards, and charity to media organizations, including $38 million to so-called “investigative journalism” centres.

According to Mint Press News (MPN), which sorted through over 30,000 documents, Bill Gates has given roughly $38 million to investigate journalism centres aimed at training journalists. Of this sum, over $20 million has gone to the International Center for Journalists, which “builds the expertise and digital skills journalists need to deliver trustworthy news essential for vibrant societies.”

The generous donations given to the ICFJ over several years have been given with the express purpose of producing journalists who focus on “data-driven health and development news reports to help African media to better contribute to setting development agendas and furthering public accountability,” according to the Bill and Melinda Gates Foundation’s website.

Producing health-obsessed investigative journalists is a common trend with Gates.

According to the Foundation’s website, the Premium Times Centre for Investigative Journalism received its grant ($3,800,357) to “support sustained high-quality, evidence-based, and solutions-oriented media coverage of global health and development issues in Primary Health Care systems, Agriculture & Financial Inclusion.”

Other recipients of over $1 million include The Pulitzer Center for Crisis Reporting ($2,432,552) to “support editorial projects focused on global health issues,” Fondation EurActiv Politech ($2,368,300), International Women’s Media Foundation ($1,500,000), Center for Investigative Reporting – $1,446,639, InterMedia Survey institute ($1,297,545), and The Bureau of Investigative Journalism ($1,068,169).

Put simply, it appears Bill Gates wants to install a personal army of professional scrutineers in various media outlets that disseminate his position on healthcare and propaganda about public officials who deviate.

Gates also, of course, funds the journalism programs of several universities, including Johns Hopkins University, Columbia University, the University of California Berkeley, Tsinghua University, Seattle University, Rhodes University, and Montclair State University.

Harvard University (of which Gates is a dropout), the University of Southern California, Boston University, and Ahmadu Bello University have also received money from Gates’ Foundation to take on various media projects.

Producing new journalists isn’t the only area in media that Gates is focusing on, though. He also targets experienced journalists in legacy media organizations. According to MPN’s report, a total of $166.2 million has been given to well-known legacy media organizations.

“The money is generally directed towards issues close to the Gateses hearts. For example, the $3.6 million CNN grant went towards “report[ing] on gender equality with a particular focus on least developed countries, producing journalism on the everyday inequalities endured by women and girls across the world,” while the Texas Tribune received millions “to increase public awareness and engagement of education reform issues in Texas.” Given that Bill is one of the charter schools’ most fervent supporters, a cynic might interpret this as planting pro-corporate charter school propaganda into the media, disguised as objective news reporting,” reports MPN.

Just over one decade ago, Bill Gates was under fire for his attempt to control the media through spread-out donations, but this fire seems to have flickered out until recently.

“Beyond their subject matter, these [health report stories] have something else in common: They were all bankrolled by the Bill & Melinda Gates Foundation,” the Seattle Times wrote in 2011.

“Better-known for its battles against global disease, the giant philanthropy has also become a force in journalism.”

“The foundation’s grants to media organizations such as ABC and The Guardian, one of Britain’s leading newspapers, raise obvious conflict-of-interest questions: How can reporting be unbiased when a major player holds the purse strings?”

Unsurprisingly, the Seattle Times and the Blethen Corporation do not appear to have ever received money from Bill Gates.

May 22, 2022 Posted by | Corruption, Full Spectrum Dominance | , | 1 Comment

FDA Dumps More Pfizer Documents: Why Were So Many Adverse Events Reported as ‘Unrelated’ to Vaccine?

By Michael Nevradakis, Ph.D. | The Defender | May 17, 2022

The latest release of Pfizer-BioNTech COVID-19 vaccine documents raises questions about how frequently adverse events experienced by clinical trial participants were reported as “unrelated” to the vaccine.

The 80,000-page document cache released May 2 by the U.S. Food and Drug Administration (FDA) includes an extensive set of Case Report Forms (CRFs) from Pfizer trials conducted at various locations in the U.S.

The documents also include the “third interim report” from BioNTech’s trials conducted in Germany (accompanied by a synopsis of this report and a database of adverse events from this particular set of trials).

The FDA released the documents, which pertain to the Emergency Use Authorization (EUA) of the vaccine, as part of a court-ordered disclosure schedule stemming from an expedited Freedom of Information Act (FOIA) request filed in August 2021.

Public Health and Medical Professionals for Transparency, a group of doctors and public health professionals, submitted the FOIA request.

Adverse events during Pfizer vaccine trials in the U.S. usually reported as ‘unrelated’ to vaccination

Pfizer conducted a series of vaccine trials at various locations in the U.S., including the New York University Langone Health Center, Rochester Clinical Research and Rochester General Hospital (Rochester, New York) and the J. Lewis Research, Inc. Foothill Family Clinic (Salt Lake City, Utah).

The Pfizer documents released this month by the FDA included a series of CRFs for patients who suffered some type of adverse event during their participation in the COVID-19 vaccine trials.

As the documents reveal, despite the occurrence of a wide range of symptoms, including serious cardiovascular events, almost none were identified as being “related” to the vaccine.

Such serious yet “unrelated” adverse events included:

Of the CRFs found in the documents released this month, only one adverse event is clearly specified as being related to the vaccination: a participant who suffered from psoriatic arthritis, with no prior history of the condition.

In addition, several CRFs indicated exposure during pregnancy (see here and here), or during a partner’s pregnancy (see here and here). However, the documents provided do not appear to have provided any follow-ups regarding any outcomes or potential adverse events for the participants, their partners or their newborn babies once born.

In some instances, while the CRFs claimed the adverse events suffered by patients were not related to the vaccine, their cause was unspecified, simply indicated as “other,” while in another case, a participant’s “unplanned” small bowel obstruction and panic attacks were listed as being unrelated to the vaccination despite no relevant medical history pertaining to the SAEs (severe adverse events) in question.

Did Pfizer hide critical information from regulators?

It is difficult to draw concrete conclusions about any specific case from the data provided by CRFs and vaccine trial summaries.

However, what raises eyebrows is the very large number of adverse events — often serious and often requiring the hospitalization of the patients involved — that were determined to be “unrelated” to the administration of the COVID vaccine.

Previously released Pfizer documents also included discrepancies in the recording of adverse events.

According to investigative journalist Sonia Elijah, these discrepancies include:

  • Trial participants were entered into the “healthy population” but were, in actuality, far from healthy.
  • SAE numbers were left blank.
  • Barcodes were missing from samples collected from trial participants.
  • The second vaccine dose was administered outside the three-week protocol window.
  • New health problems were dismissed as “unrelated” to the vaccination.
  • A remarkable number of patients with an observation period of exactly the same duration — 30 minutes, with very little variety in observation times and raising questions as to whether patients were adequately observed or were put at risk.
  • Oddities pertaining to the start and end dates of SAEs – for instance, a “healthy” diabetic suffered a “serious” heart attack on October 27, 2020, but the “end” date for this SAE is listed as the very next day, even though the patient was diagnosed with pneumonia that same day.
  • Impossible dating: in the aforementioned example of the patient who sustained a heart attack and pneumonia, the individual in question later died, but the date of death is indicated as the day before the patient was recorded as having gone to a “COVID ill” visit.
  • Unblinded teams, who were aware of which patients received the actual vaccine or a placebo, were responsible for reviewing adverse event reports, potentially leading to pressure to downplay COVID-related events in the vaccinated, or to indicate that adverse events were related to the vaccine.
  • Other adverse events were indicated as “not serious” despite extensive hospital stays, of up to at least 26 days in the case of one patient who suffered a fall which was classified as “not serious,” yet facial lacerations sustained as a result of the fall were attributed to hypotension (low blood pressure).

Many of these practices seem to appear in the trial-related documents released this month.

Medical and scientific experts who spoke to The Defender expressed similar concerns about what this month’s tranche of documents reveals, and addressed cases of “disappearing” adverse events.

Brian Hooker, chief scientific officer for Children’s Health Defense, remarked:

“I’m most concerned about ‘disappearing’ patients. One cannot conduct a valid trial and simply omit the results that they don’t like!

“With the stories about Maddie de Garay and Augusto Roux surfacing, I have to wonder how many other participants were dropped in order to hide vaccine adverse events/effects.

“If you look at the data in VAERS [Vaccine Adverse Event Reporting System], COVID-19 vaccines are the most dangerous ever introduced into the population.”

Dr. Madhava Setty, a board-certified anesthesiologist and senior science editor for The Defender, said:

“The ‘unrelated’ label the investigators use to divert attention from AEs [adverse events] is a powerful point that stands on its own. We haven’t pushed back on this enough.

“Equivalently, we can say that the meager and short-lived benefit of these shots is also ‘unrelated’ using their ‘standards.’ On what grounds can they say that their product is preventing infection (which it isn’t anymore), or death (marginally)?

“They cannot have it both ways. They cannot claim a benefit through short-term outcomes while denying that side effects of any kind are related to their product.

“That’s the whole point of doing a trial. You cannot prove causation, only statistically significant correlation.”

Setty provided further context for his remarks in an April 2022 article for The Defender and in a March 2022 presentation, in which he discussed the number of these adverse events and how Pfizer swept them away (timestamp 24:00).

In Setty‘s view:

“There’s a high likelihood of malfeasance going on. [Pfizer whistleblower] Brook Jackson says the PIs [principal investigators] were unblinded. If true, it would make it very easy for the investigators to bump up the AEs in the placebo group while ignoring some of the AEs in the vaccine group.

“Pfizer claims that 0.5% of placebo recipients suffered a serious adverse event compared to 0.6% in the vaccine group. This is how these events were obscured.”

The extant body of evidence indicates Pfizer “is hiding critical information from regulators,” Setty said:

“The clincher is in the memorandum to the VRBPAC [Vaccines and Related Biological Products Advisory Committee] (Table 2, efficacy populations), where they show us that five times more people in the vaccine group were pulled out of the trial than the placebo within seven days of their second shot for ‘important protocol deviations.’

“In a trial that big the chances that could have happened coincidentally is infinitesimally small (less than 1 in 100,000).

“Moreover, months later, the same thing happened in the pediatric trial (Table 12). This time, six times more children were pulled from the trial after their second dose.

“There are, of course, procedural differences when administering a placebo versus the mRNA vaccine, but why didn’t it happen after the first dose as well?

“Mathematically, that is about as close as you can get to eliminating any ‘shadow of doubt.’ With a formal allegation by a trial coordinator that states the same thing [referring to whistleblower Brook Jackson], we can be assured Pfizer is hiding critical information from regulators.”

BioNTech trials in Germany claim few adverse events ‘related’ to vaccine

The BioNTech trial in Germany tested various dosages of two COVID-19 vaccine formulas, labeled BNT162b1 and BNT162b2 — the latter granted EUA by the FDA.

The latest cache of Pfizer documents suggests a pattern, similar to the one in the U.S. trials, of not reporting adverse events as related to the vaccine.

According to the third interim report, dated March 20, 2021, among trial participants who were administered the BNT162b2 candidate vaccine granted EUA in the U.S.:

  • 87% of younger participants reported solicited local reactions, and 88% reported solicited systemic reactions, with 10% reporting solicited systemic reactions of Grade 3 or higher.
  • 87% of younger participants experienced “mild” solicited local reactions, and 35% experienced “moderate” solicited local reactions.
  • 88% of younger participants experienced “mild” solicited systemic reactions, and 38% experienced “moderate” solicited systemic reactions. As stated in the report:

“The most frequently reported solicited systemic reactions of any severity were fatigue (n=40, 67%), followed by headache (n=32, 53%), malaise (n=24, 40%), and myalgia (n=23, 38%). The remaining symptom terms were less frequent.

“For nausea, headache, fatigue, myalgia, chills, arthralgia and malaise each symptom was assessed as severe in <10% of participants.”

  • 43% of younger participants reported a total of 51 unsolicited TEAEs (treatment-emergent adverse events, referring to conditions not present prior to treatment or that worsened in intensity after treatment) within 28 days of the first or second dose, nine of which were deemed to be “related” to the vaccination. One participant in this category sustained a TEAE assessed as Grade 3 or higher, but “which was assessed as not related by the investigator.”
  • TEAEs among younger participants included hypoaesthesia, lymphadenopathy, heart palpitations, external ear inflammation, blepharitis, toothache, non-cardiac chest pain, cestode infection, oral herpes, tonsillitis, neck pain, insomnia, anosmia and dysmenorrhea.
  • No unsolicited treatment-emergent serious adverse events (TESAEs) or deaths were reported among younger participants, but one discontinued participation due to moderate nasopharyngitis.
  • One younger participant “discontinued due to a moderate AE (nasopharyngitis).”
  • 86% of older participants reported solicited local reactions, with 6% reporting solicited local reactions of Grade 3 or higher, 78% reporting “mild” solicited local reactions and 36% reporting “moderate” solicited local reactions.
  • 72% of older participants reported solicited systemic reactions, with 11% of these participants sustaining solicited systemic reactions of Grade 3 or higher, 69% sustaining “mild” solicited reactions and 36% sustaining “moderate” solicited reactions.
  • 33% of older participants reported a total of 20 unsolicited TEAEs, four of which were determined to be “related” to the vaccination. Among older participants, 8% reported a TESAE of Grade 3 or higher, with “one event assessed as related by the investigator.”
  • One older participant was reported to have sustained a “not related TESAE” (an ankle fracture).
  • TESAEs among older participants included back pain, chest pain, facial injury, increased lipase, increased amylase, muscle spasms, musculoskeletal pain, tendon pain, orthostatic intolerance, renal colic, seborrhoeic dermatitis and “painful respiration.”

Among trial participants who received the BNT162b1 candidate vaccine (not granted EUA):

  • 86% of “younger participants” reported solicited (expected) localized reactions (remaining in one part of the body), with 18% reporting Grade 3 or higher solicited local reactions, 86% of younger participants reporting “mild” solicited local reactions and 54% reporting “moderate” solicited local reactions.
  • 92% of younger participants reported solicited systemic reactions (spreading to other parts of the body), with 44% reporting Grade 3 or higher solicited systemic reactions, 90% reporting “mild” solicited systemic reactions and 74% experiencing “moderate” solicited systemic reactions.

The report states:

“The most frequently reported solicited systemic reactions of any severity were fatigue (n=68, 81%), headache (n=66, 79%), myalgia (n=51, 61%), malaise (n=50, 60%), and chills (n=47, 56%). The remaining symptom terms were less frequent.

“For nausea, vomiting, diarrhea, myalgia, arthralgia and fever each symptom was assessed as severe in ≤10% of participants.”

  • 45% of younger participants reported a total of 83 unsolicited (unexpected) TEAEs within 28 days of receiving the first or second dose.

A total of 51 of these unsolicited TEAEs were reported as “related” to the vaccination, while 2% of participants sustained Grade 3 or higher TEAEs (four in total), “of which three events were assessed as related by the investigator.”

No unsolicited TESAEs or deaths were reported in this category.

  • According to the report, among younger participants, TEAEs included:

“‘General disorders and administration site conditions’ reported by 9 participants (11%),” including influenza-like illness and injection site hematoma.

“‘Nervous system disorders’ reported by 10 participants (12%),” including presyncope, hyperaesthesia, paraesthesia, and headache.

“‘Respiratory, thoracic and mediastinal disorders’ reported by 9 participants (11%),” including cough and oropharyngeal pain.”

Other symptoms included back pain, musculoskeletal chest pain, cervicobrachial syndrome, taste disorder, sleep disorder, depression, hallucination, dysmenorrhoea, pruritus and pityriasis rosea, while one participant required the excision (removal) of a papilloma.

  • One younger participant discontinued participation in the trial, “due to a moderate AE (malaise),” while another participant discontinued participation “due to dose-limiting toxicity.”
  • 83% of “older participants” reported solicited local reactions, but none were reported as Grade 3 or higher, while 83% of solicited local reactions were “mild” and 42% were “moderate.”
  • 92% of older participants reported solicited systemic reactions, with 28% of participants experiencing Grade 3 or higher solicited systemic reactions, 89% experiencing “mild” solicited systemic reactions, and 61% experiencing “moderate” solicited systemic reactions.

According to the report:

“The most frequently reported solicited systemic reactions of any severity were headache (n=29, 81%), fatigue (n=27, 75%), myalgia (n=18, 50%), and malaise (n=18, 50%). The remaining symptom terms were less frequent.”

  • 36% of participants reported a total of 24 unsolicited TEAEs within 28 days of the first or second dose, nine of which were assessed as “related” to the vaccination.

Of the participants in this category, 11% reported TEAEs of Grade 3 or higher (four events in total), with one of these events assessed as “related” to the vaccination.

  • TEAEs reported by older participants included oropharyngeal pain, nasopharyngitis, bladder dysfunction, sleep disorder, musculoskeletal pain and musculoskeletal chest pain, pollakiuria, migraine, syncope and alopecia.
  • One older participant receiving the BNT162b1 candidate sustained a TESAE (syncope), and there were no deaths in this category.

Of note, none of the participants for either vaccine candidate were pregnant, which raises questions about recommending and administering the vaccine to pregnant women despite the absence of any clinical trial data.

As the documents show, a wide range of adverse effects were reported, including cardiovascular and nervous system conditions, most of which were determined to be unrelated to the vaccination itself.

Michael Nevradakis, Ph.D., is an independent journalist and researcher based in Athens, Greece.

© 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

May 22, 2022 Posted by | Deception, Science and Pseudo-Science | , , , | 3 Comments

Monkeypox Fears May Rescue Endangered Corporations

By Whitney Webb | Unlimited Hangout | May 20, 2022

In recent days, concern over a global outbreak of monkeypox, a mild disease related to smallpox and chickenpox, has been hyped in the media and health ministries around the world, even prompting an emergency meeting at the World Health Organization (WHO). For some, fears have centered around monkeypox being the potential “next pandemic” after Covid-19. For others, the fear is that monkeypox will be used as the latest excuse to further advance draconian biosecurity policies and global power grabs.

Regardless of how the monkeypox situation plays out, two companies are already cashing in. As concern over monkeypox has risen, so too have the shares of Emergent Biosolutions and SIGA Technologies. Both companies essentially have monopolies in the US market, and other markets as well, on smallpox vaccines and treatments. Their main smallpox-focused products are, conveniently, also used to protect against or treat monkeypox as well. As a result, the shares of Emergent Biosolutions climbed 12% on Thursday, while those of SIGA soared 17.1%.

For these companies, the monkeypox fears are a godsend, specifically for SIGA, which produces a smallpox treatment, known by its brand name TPOXX. It is SIGA’s only product. While some outlets have noted that the rise in the valuation of SIGA Technologies has coincided with recent concerns about monkeypox, essentially no attention has been given to the fact that the company is apparently the only piece of a powerful billionaire’s empire that isn’t currently crumbling.

That billionaire, “corporate raider” Ron Perelman, has deep and controversial ties to the Clinton family and the Democratic party as well as troubling ties to Jeffery Epstein. Aside from his controlling stake in SIGA, Perelman has recently made headlines for rapidly liquidating many of his assets in a desperate bid for cash.

Similarly, Emergent Biosolutions has also been in hot water. The company, which has troubling ties to the 2001 Anthrax attacks, came under fire just under two weeks ago for engaging in a “cover up” over quality control issues relating to their production of Covid-19 vaccines. A Congressional investigation found that quality control concerns at an Emergent-run facility led to more than 400 million doses of Covid-19 vaccines being discarded. The Emergent factory in question had been shut down by the FDA in April 2021. They were allowed to reopen last August before the government terminated the contract. Given that the majority of the company’s business is tied to US government contracts, the loss of this contract, and the accompanying poor publicity, the news that its smallpox vaccine may soon be of international interest is likely seen as a godsend by the company.

Notably, this is the second time in a year that both companies have benefitted from pandemic or bioterror fears propagated by the media. Last November, speculation rose that a re-emergence of the eradicated virus that causes smallpox would soon take place. This first began with Bill Gates’ comments on the prospects of smallpox bioterrorism during a November 4th, 2021 interview and was followed by the November 16th announcement of a CDC/FBI investigation into 15 suspicious vials labeled “smallpox” at a Merck facility in Philadelphia. Now, roughly six months later, the same fears are again paying off for the same two companies.

A Killer Enterprise

Emergent Biosolutions was previously known as BioPort. The company was founded by Fuad el-Hibri, a Lebanese businessman, who leveraged his contacts with powerful US former military officials and politicians, to take control of a flailing Michigan factory. It was the only factory authorized to produce an anthrax vaccine.

The anthrax vaccine was known to have major problems even before BioPort had acquired it, and is believed by many investigators to be one of the main causes of “Gulf War” syndrome. The vaccine itself, originally developed at Fort Detrick, had little to no safety track record at the time it was administered to US troops in the First Gulf War – a problem that was never remedied. However, its chronic safety issues and its clumsy, multi-dose regimen would later prompt BioPort/Emergent Biosolutions to spend years developing a new formulation of its anthrax vaccine.

The creation of BioPort coincided with the Clinton administration’s efforts to mandate the anthrax vaccine for all members of the US Armed Forces. With control over the only source of anthrax vaccine, BioPort was poised to make a killing.

Once the company acquired the Michigan facility, it took large amounts of US government funds, ostensibly to make improvements at the site. However, the company declined to use the funds to make the necessary repairs, instead spending that money on its executives’ offices, as opposed to the vaccine factory, and millions more on bonuses for “senior management.” Pentagon auditors would later find that still millions more had gone “missing” and BioPort’s staff were unaware of the cost of producing a single dose of the vaccine. Despite the clear mismanagement and corruption, BioPort demanded to be bailed out by the Pentagon, and they were. Meanwhile, the Michigan facility lost its license after a government inspection found numerous safety issues.

However, by August 2001, BioPort stood to lose the Pentagon contracts – its only source of income. The Pentagon began preparing a report, due to be released in September 2001, that would detail a plan for letting BioPort go. Thanks to the September 11, 2001 attack on the Pentagon, that report was never released. Shortly thereafter, the 2001 anthrax attacks began.

Just months before, BioPort had contracted Battelle Memorial Institute to help rescue its flailing vaccine program. The deal gave Battelle “immediate exposure to the vaccine” and it was used in connection with the Pentagon-funded, gain-of-function anthrax program that involved both Ken Alibek and William C. Patrick III, two bioweapons experts with deep ties to the CIA. That program was housed at Battelle’s West Jefferson facility in Ohio. That facility is believed by many investigators to be the source of the anthrax used in the 2001 attacks.

The ensuing panic from the anthrax attacks led the Department of Health and Human Services (HHS) to intervene. They gave BioPort its license back in January 2002 despite persisting safety concerns at its vaccine production facility in Michigan. BioPort was not content to merely see its past contracts with the Pentagon restored, however, as it began lobbying heavily for new contracts for anthrax vaccines intended for American civilians, postal workers and others. They would get them, largely thanks to HHS’ then-counter-terrorism adviser and soon to be HHS’ newest Assistant Secretary — Jerome Hauer. Hauer would later join the board of BioPort, after it reformed as Emergent Biosolutions, in 2004.

Such examples of cronyism are more common than not when it comes to Emergent Biosolutions. Indeed, the company has frequently relied on individuals who spend their careers passing through the “revolving door” between the pharmaceutical industry and government, particularly those who also moonlight as bioterror alarmists. One of the main individuals critical to the company’s success over the years has been Robert Kadlec. Kadlec served as the top bioterror advisor to the Pentagon in the weeks leading up to the 2001 anthrax attacks. Months prior, he had participated in the June 2001 simulation Dark Winter, which “predicted” major aspects of the subsequent anthrax attacks. Kadlec subsequently crafted much of the legislation that would create the country’s subsequent bioterror/pandemic response policy, including BARDA and the Strategic National Stockpile.

Soon after leaving government, Robert Kadlec helped found a new company in 2012 called “East West Protection,” which develops and delivers “integrated all-hazards preparedness and response systems for communities and sovereign nations.” The company also “advises communities and countries on issues related to the threat of weapons of mass destruction and natural pandemics.”

Kadlec formed the company with W. Craig Vanderwagen, the first HHS Assistant Secretary for Preparedness and Response (a position Kadlec had helped write into law and would later hold himself). The other co-founder of East West Protection was Fuad El-Hibri, the founder of BioPort/Emergent Biosolutions, who had just stepped down as Emergent’s CEO earlier that year.

Kadlec then became a consultant. Kadlec’s consultancy firm, RPK Consulting, netted him $451,000 in 2014 alone, where he directly advised Emergent Biosolutions as well as other pharmaceutical companies like Bavarian Nordic. Kadlec was also a consultant to military and intelligence contractors, such as the DARPA-backed firm Invincea and NSA contractor Scitor, which was recently acquired by SAIC.

Kadlec would return to government as HHS ASPR under Trump, a position which he held at the time the Covid-19 crisis began. The year prior, in 2019, Kadlec had conducted a months-long simulation focused on a global pandemic originating in China called Crimson Contagion. Once the Covid-19 crisis began in earnest, he played a major role in securing Covid-19 vaccine contracts for Emergent Biosolutions, despite his conflicts of interest, some of which he had declined to disclose upon being appointed to serve as ASPR.

Emergent Biosolutions’ pattern of corrupt behavior, beginning with its anthrax vaccine, can be seen with its recent actions as it relates to its production of Covid-19 vaccines. Per the recent Congressional report, released just days before the recent spike in concern over monkeypox began, Emergent lab workers “intentionally sought to mislead government inspectors about issues” at its Baltimore-based plant and also repeatedly “rebuffed” efforts by AstraZeneca and Johnson & Johnson to inspect their facilities. “Despite major red flags at its vaccine manufacturing facility, Emergent’s executives swept these problems under the rug and continued to rake in taxpayer dollars,” House Oversight and Reform Committee Chairwoman Carolyn Maloney (D-NY) stated upon the report’s release. Yet such “major red flags” can be found throughout the company’s entire history, for those willing to take the time to look.

Just days after the Congressional report was released, Emergent Biosolutions announced that it would acquire the exclusive worldwide rights to the “first FDA-approved Smallpox Oral Antiviral for all ages” from the company Chimerix. The drug, called TEMBEXA, is only for the treatment of smallpox, which the company refers to as “a high priority public health threat.” The press release on the company’s acquisition of TEMBEXA states that multi-million US government contracts for the product are anticipated. The FDA formally approved the drug last June.

Emergent Biosolutions also has the rights to the smallpox vaccine known as ACAM2000, which can also be used to treat monkeypox. The vaccine, originally produced by Sanofi, was acquired by the company in 2017. As a result, the company has an essential monopoly over smallpox vaccines as ACAM2000 is “the only vaccine licensed by the FDA for active immunization against smallpox disease for people determined to be at high risk of smallpox infection.”

Given their track record, it’s worth asking why Emergent Biosolutions has been working in recent months to pivot much of its business into smallpox treatments. However, there is no speculation needed when observing that the current monkeypox fears and helping rescue the company, whose shares had fallen some 26% year to date before concern over the recent monkeypox outbreak began to grow.

Whatever comes of the monkeypox situation, Emergent Biosolutions’ decades-long track record is undeniably one of corruption and cronyism.

BioArmor” for Ron Perelman’s Flailing Business Empire

SIGA Technologies, which likens its products to “Human BioArmor”, features a quote from Bill Gates at the top of its about page. The quote reads: “[…] the next epidemic could originate on the computer screen of a terrorist intent on using genetic engineering to create a synthetic version of the smallpox virus […]” The quote is from Bill Gates’ speech to the 2017 Munich Security Conference, where he used the threat specifically of smallpox to argue that “health security” and “international security” be merged. Notably, last March, the Munich Security Conference hosted a simulation of a global pandemic caused by a “genetically engineered monkeypox virus.”

SIGA is one example of a company that seeks to find its niche in the middle of “health security” and “international security.” It specifically provides “solutions for unmet needs in the health security market that comprises medical countermeasures against chemical, biological, radiological, and nuclear (CBRN) threats, as well as emerging infectious diseases.” The majority of contracts for CBRN medical countermeasures in the US are funded by the Pentagon. While it promotes itself as a CBRN threat-focused company, SIGA is, for now, singularly focused on smallpox.

Indeed, SIGA Technologies is only currently profitable in the event of an actual outbreak of smallpox or a related disease, or when fear of a smallpox bioterror event is high. Specifically, concern over the latter has led to the company to win government contracts to produce TPOXX for the Strategic National Stockpile (SNS). This is because TPOXX is only used to treat active smallpox or monkeypox infection, not prevent it. This means that it is only useful if smallpox, monkeypox or a related disease is actively infecting people or if there is a high risk that one of these diseases will soon infect large groups of people. TPOXX was first approved in 2018 by the FDA and was approved by the European Medicine Agency (EMA) this past January. The FDA approved an intravenous version of TPOXX just this past Thursday. Overall, SIGA has received over $1 billion from the US government to develop TPOXX.

SIGA is currently partnered with HHS’ BARDA, the Department of Defense, the CDC and the NIH. Another partner is Lonza, a European pharmaceutical manufacturing firm that is partnered with both the World Economic Forum and Moderna. SIGA’s CEO, Phillip Gomez, is an alumni of PRTM Consulting, where he would have worked closely with Robert Kadlec, as the two men overlapped as directors of the firm and both worked advising government agencies on matters of public health and biodefense.

SIGA is also notable because it is possibly the only company in the business empire of corporate raider Ron Perelman that is not attached to growing mountains of debt. Perelman is one of the notorious corporate raiders from the 1980s who conducted corporate takeovers fueled by junk bonds, particularly those connected to Michael Milken’s Drexel Burnham Lambert. Perelman’s business tactics have long been informed by his volcanic temper and his ruthlessness, with former Salomon Brothers CEO John Gutfruend once remarking that “believing Mr. Perelman has no hostile intentions is like believing the tooth fairy exists.”

Perelman is also known for being a long-time patron of the Clinton family, even though, more recently he donated to Donald Trump’s political campaigns. Perelman apparently first became interested in courting influence with the Clintons after marrying Patricia Duff in 1994. Duff was deeply connected to the Democratic Party, having worked for Democratic pollster Pat Cadell, and she had also worked for the House panel that “investigated” the assassinations of John F. Kennedy and Martin Luther King Jr. Prior to marrying Perelman, she had been married to movie mogul Michael Medavoy and had “introduced Clinton to the Hollywood establishment,” according to the Washington Post.

As Perelman’s wife, Duff styled herself a leading Democratic fundraiser, with the 1995 fund-raising dinner being emblematic of that. Also, in 1995, Perelman attended a $1,000-a-plate dinner in New York for the Clintons, where Perelman sat across from the President, as well as a state dinner for Brazil’s president at the White House.

For Perelman, his generosity to the Clinton political machine resulted in an appointment by Clinton to the board of trustees of the Kennedy Center in 1995. Other, less public gestures from the Clintons were likely, as Perelman offered much more to the First Family than he appears to have received in return. Perhaps most notable of Perelman’s favors for Bill Clinton was his offering of jobs to scandal-ridden members of his administration, Webster Hubbell and Monica Lewinsky, in the wake of their respective controversies. However, after the job offers were publicly reported, both Hubbell and Lewinsky were let go, though the offers later caught the attention of independent counsel Ken Starr. Starr never subpoenaed or investigated Perelman or the offers he had made to Hubbell or Lewinsky.

The controversial hirings had been arranged between Perelman and Clinton advisor Vernon Jordan, who sat on the board of Revlon, a Perelman-controlled company, while his wife was on the board of another Perelman-owned firm. Jordan was known as Clinton’s “conduit to the high and mighty” and had taken Clinton to the 1991 Bilderberg conference. On the decision to hire Lewinsky following the scandal, a former business associate of Perelman’s told the Washington Post that “It’s like the Mafia, it’s all done in code,” adding that “I can assure you that Ronald made the decision to give Lewinsky the job. And I can assure you he wouldn’t want to know why Jordan was asking.”

In 1995, Perelman held a Clinton fundraiser at his mansion, with guests including singer Jimmy Buffett, Miami Vice actor Don Johnson, actor Michael Douglas’ then-wife Deandra and DNC co-chair Don Fowler. Other guests included A. Paul Prosperi, a corrupt Clinton crony, and the now infamous Jeffrey Epstein. Clinton himself attended the fundraiser. According to the Palm Beach Post, guests had donated at least $100,000 to the DNC to attend the dinner with the President. This was, of course, in the lead up to the 1996 election, and the DNC would later come under heavy scrutiny due to illegal fundraising. This fundraiser was not Epstein’s only interaction with Perelman – Perelman would later be listed as a frequent dinner guest of Epstein’s in the 2003 Vanity Fair profile penned by Vicky Ward and is listed in Epstein’s black book of contacts.

For most of the 2000s, Perelman has sat atop a massive, ever-growing fortune. Yet, since 2020, Perelman has “been unloading assets ‘A lot of them. Rapidly.’” It started with sales of valuable paintings at Sotheby’s and soon extended to Perelman’s investment company MacAndrews & Forbes, which disposed of its interest in two companies that same year, including $1 billion in shares in Scientific Games. According to MoneyWeek, Perelman’s net worth dropped from $19 billion in 2018 to $4.2 billion in late 2020, “prompting speculation that he’s running out of money.” Over the course of last year, Perelman has continued to “downsize”, looking to sell off his estate in the Hamptons for $115 million, another 57-acre estate worth $180 million and two townhouses in Manhattan’s Upper East Side for $60 million.

Other assets held by Perelman’s company MacAndrews & Forbes are also drowning in debt. One of the few assets of the company that isn’t currently haemorrhaging money or struggling with debt is its shares in SIGA Technologies. Perelman’s main company, MacAndrews & Forbes, has long been one of SIGA’s biggest investors and remains its largest shareholder, controlling 33% of all shares.

Since Perelman got involved with SIGA, accusations of corruption have plagued the company. For instance, in May 2011, SIGA was given a no-bid contract worth about $433 million to develop and produce 1.7 million doses of anti-viral drug for smallpox. At the time there was no evidence the smallpox drug in question was capable of treating the disease and there was alarm among some HHS staffers that SIGA’s return on investment from the contract was “outrageous.” The contract began to be investigated over concerns that the contract had been awarded to SIGA precisely because it was controlled by Perelman, who had donated heavily to Barack Obama. At the time, CNN noted the following about Perelman’s connections to the Obama White House:

“Ronald Perelman is controlling shareholder of Siga Technologies and a longtime Democratic Party activist and fundraiser. He’s also a large contributor to Republicans, but has been a particular friend of the Obama White House.

Also on Siga’s board of directors is Andy Stern, former president of the Service Employees International Union, who has had close relations with the Obama administration and who has supported President Barack Obama’s health care initiatives.”

As a result of these concerns and the potential conflict of interest, a congressional investigation began. Days after learning that this key government contract may be in jeopardy, SIGA executives sold off large amounts of company stock at an average price of $13.46 per share, netting its Chief Executive Officer and Chief Scientific Officer at the time millions of dollars. A month later, the company announced that its contract had been downsized and shares in the company fell to under $2 by that December.

Given past “pay-to-play” accusations around Perelman’s role in the firm during the Obama administration, when President Joe Biden served as Vice President, what are we to make of the recent media hype around monkeypox? Or concerns raised last year of a bioterrorism event involving smallpox?

Perhaps it’s more important to ask other questions – why has Perelman’s role in SIGA been largely obfuscated or totally ignored by recent reporting on the company? Similarly, why has Emergent Biosolutions’ horrific track record also been excluded from recent reports, including the major complaints from Congress made against the company less than two weeks ago? It seems the fear being generated around monkeypox is not only boosting shares for these two rotten companies, it’s helping the public forget their past sins.

Whitney Webb has been a professional writer, researcher and journalist since 2016. She has written for several websites and, from 2017 to 2020, was a staff writer and senior investigative reporter for Mint Press News. She currently writes for The Last American Vagabond.

May 22, 2022 Posted by | Corruption, Deception, Science and Pseudo-Science, Timeless or most popular | , , , , , | 1 Comment

Pandemic 2: Monkeypox Madness

OffGuardian | May 21, 2022

Monkeypox – it’s the hip new disease sweeping the globe. Allegedly appearing almost simultaneously in over a dozen different countries on four different continents.

As we wrote in the early days of the Covid “pandemic”, the only thing spreading faster than the disease is fear.

The media reported the first UK case of monkeypox on the 7th of May. Less than two weeks later, we’re seeing some very familiar headlines. Just like that…Pandemic 2: Monkey Pox!! begins playing at all your favorite fear porn outlets.

Sky News tells us that UK Monkeypox “cases” have “doubled(!)”… from 10 to 20.

The BBC went real subtle with it, blaring“Monkeypox: Doctors concerned over impact on sexual health”

The New Scientist has actually used the P-word, asking “Can Monkeypox become a new pandemic?”, before answering, essentially, “probably no, but also maybe yes!”. Keeping their options open.

Science warns that “Monkeypox outbreak questions intensify as cases soar”

The Mirror has gone full paranoid already, headlining:

Russia looked into using monkeypox as biological weapon, claims ex soviet scientist

So that’s one direction the story might go.

To be clear, “monkeypox” (whatever that even means in this context), is NOT a Russian bio-weapon. It’s not a Western bio-weapon either. Or Chinese bio-weapon. It’s just another scare story. And a rushed, half-hearted one at that.

One of the signs that marked the Covid “pandemic” as a psy-op from an early stage was the sheer speed with which the hysteria spread. Far from learning from their mistakes, the powers-that-be have decided to go even faster this time.

Despite “cases” numbering barely in the dozens, the World Health Organization has called an emergency meeting, a strange thing to do when their annual Assembly starts literally tomorrow. But I guess when your launching a new product you need to do everything you can to get the hype going.

Despite just two “cases” in the entire United States (and indeed the fact they still don’t work), New York is bringing back mask recommendations.

Nobody has said “lockdown”… yet. But Hans Kluge, WHO regional director for Europe, is “concerned” that transmission could accelerate if people attend mass gatherings:

as we enter the summer season … with mass gatherings, festivals and parties, I am concerned that transmission could accelerate”.

(As inflation soars and the cost of living crisis only gets worse, it’s probably handy for them to have a new “public health” reason to ban protests or clampdown on civil unrest. Just a thought.)

There’s some good news though… for vaccine manufacturers, anyway. As Whitney Webb reports, two struggling pharmaceutical companies have already seen a big stock boost from the “outbreak”:

Regardless of how the monkeypox situation plays out, two companies are already cashing in. As concern over monkeypox has risen, so too have the shares of Emergent Biosolutions and SIGA Technologies. Both companies essentially have monopolies in the US market, and other markets as well, on smallpox vaccines and treatments. Their main smallpox-focused products are, conveniently, also used to protect against or treat monkeypox as well. As a result, the shares of Emergent Biosolutions climbed 12% on Thursday, while those of SIGA soared 17.1%.

Just as with Covid, and despite rumours they would be leaving the World Health Organization, Russia appears to be lining up with the WHO agenda. Already they are “tightening border quarantine” rules, vaccinating healthcare workers and supplying quick bedside tests internationally.

Looks like we might be in for an epic summer of scare-mongering, panic-buying & bucketloads of cringe.

💢Are the new jabs already prepped & ready to go?

💢Are the “our hospitals are overwhelmed videos” being filmed as we speak, complete with “monkey pox” moulage and crying nurses who turn out to have IMDB pages & multiple acting credits?

💢Are the sleepy masses going to be fooled yet again?

Watch this space…

May 22, 2022 Posted by | Fake News, Mainstream Media, Warmongering, Science and Pseudo-Science | | 2 Comments

The terrifying risks of genetic experimentation

By Guy Hatchard | TCW Defending Freedom | May 22, 2022

IT SAYS a lot about the primitive state of our knowledge of genetics that after two years of painstaking assessment, no consensus has been reached about the origins of coronavirus. Many geneticists have of course made up their minds based not on the highly unusual nature of the virus, but on its familiarity. It contains genetic sequences well known to science which appear to have been fudged together by researchers, possibly as part of a bioweapons programme.

Genetic engineers are the most dangerous people on the planet, putting serial killers and warmongers to shame. You may question whether it is possible to argue that genetic manipulation inevitably endangers the integrity of human DNA. The fact is that our DNA functions as part of a wider epidemiological network. Even disruption or alteration of this subsidiary network is quite sufficient to cause serious health problems.

Even fragments of genetic material pose dangers

A summary published by Nature on May 11 reports that viral fragments known as coronavirus ghosts are probably causing or complicating serious and lingering problems including long covid. They have been found to persist in the human gut for months where their continued presence can exhaust the immune system.

The extent of our current understanding of genetic function is wildly exaggerated. No geneticist can even construct a single cell organism from scratch. Not even close, a million miles away in fact. To date, what geneticists can do is fiddle about with natural genetic structures and maim their holistic function, or combine fragments from different organisms or biochemicals, rather like a five-year-old left with a book of matches and a box of fireworks.

DNA is a rigid taskmaster

Changes in genetic sequence, content, and function can and do have major consequences for genetic expression and that perforce includes our personality and social interaction. Our DNA is our rulebook, and it strictly enforces its own code in controlling our physiology and psychology. Change the rulebook and the consequences can be unpredictable.

You arrive at a football match at which, unknown to the players, the referee has been substituted. The new referee knows nothing about the rules of soccer, he has made them up and is about to rigidly enforce them. Imagine the ensuing chaos, consternation, and sheer disbelief.

Now imagine the situation if virtually all the players have such a deep belief in the authority of referees that anything that they do and say has to be accepted. There will be chaos, but no consternation or disbelief, just uninformed random mayhem.

Our genetic system commands acceptance much like the referee, our physiology and psychology has to comply. Change the DNA, its expression and function or its wider epidemiological network, even in a minor way, the physiology and psychology must respond. The consequences are going to be unpredictable, that is a known law of genetic manipulation.

Government control of the pandemic response has been a disaster

The New Zealand government claims that 95 per cent of the eligible population have received the mRNA vaccination, although only 70 per cent have been boosted, no doubt after the first shots left a bad taste and the prospect of endless jabs was daunting. mRNA inoculation has changed the way our immune system functions. Has this changed the temperament of the New Zealand population? You decide. The risks are real.

Last week Covid Response Minister Chris Hipkins struck a positive note. Requirements for pre-departure Covid testing are being phased out. He also reminded us that the Covid-19 Public Health Response Act has an in-built sunset clause and must be repealed by May 13, 2023.

Be warned, Hipkins added that he planned to incorporate its provisions into existing legislation and added that the management of the virus should become a part of the normal functioning of government.

Do you think that our government is capable of managing the outcomes of uncontrolled biotechnology experimentation? No, it is not. Biotechnologists are not honestly warning the government of risks, just as the family members of criminals often shield their black sheep and provide them with alibis.

The biotechnology industry has been operating a fraud

The commercial biotechnology industry has been running a con. The technique is to make big promises to encourage investment and grants. There is nothing too large to promise – freedom from disease, long life . . . When nothing is achieved and problems inevitably occur, you make even bigger promises and ask for more money. Nothing is said about the risks.

As a result, biotechnology has become a highly influential part of our society accounting for much of university funding and speculative investment. At root, the hype is based on an improbable dream and phantasm. In actuality, biotechnology is presenting the world with an elevated risk profile that threatens to dwarf all others.

Just think, the whole basis of our society, health, creativity, kindness, intelligence, morality, happiness, and so much more relies on the optimal operation of our DNA. Risk that and you risk everything, including even topical issues like the integrity of the global supply chain and social stability.

Time to say it clearly: we made a big mistake. Millions have died from the cure and the cause. Only the cessation of genetic experimentation can protect us from more injury, mental turmoil, deaths and global catastrophes.

May 22, 2022 Posted by | Science and Pseudo-Science, Timeless or most popular | | Leave a comment

Former head of the ruling Social Democrats, Oskar Lafontaine, blames NATO for Ukraine conflict

Samizdat | May 22, 2022

A veteran top German politician has said the West’s refusal to listen to Moscow’s concerns is one of the main causes of the current conflict in Ukraine. Oskar Lafontaine, who from 1995 until 1999 served as chair of the Social Democrats, accused the West of ignoring Russia’s security interests for years.

In an interview with left-wing newspaper Junge Welt published on Saturday, Lafontaine argued that “for a long time, we have been in a situation where Russia and China have been militarily encircled by the US.” The former SPD leader said Moscow had made it clear to NATO for 20 years that Ukraine should not become part of the military alliance – a scenario, which, according to Lafontaine, would mean US missiles deployed on the Ukraine-Russia border.

“These security interests were consistently ignored,” the politician said. And this was “one of the key reasons for the outbreak of the Ukraine war.”

Speaking of Ukraine’s NATO aspirations, the former SPD chair dismissed the argument that every country is free to decide what alliance to join.

“Everyone knows that the US would never accept Cuba’s accession to a military alliance with Russia, nor the deployment of Russian missiles on the US border with Mexico or Canada,” Lafontaine argued.

According to the German politician, Russia’s key concern in Ukraine is not NATO accession per se, but the prospect of missiles appearing on the border with minimal warning time.

Lafontaine broke down the Ukraine crisis into three key phases: firstly, NATO’s relentless eastern expansion, despite warnings from within the US that the strategy risked a conflict with Russia; secondly, President Putin’s “decision to invade Ukraine”; and thirdly, Joe Biden’s “war of attrition.”

The politician said America’s $40 billion dollar aid package for Ukraine, consisting mostly of weapons, is further “proof that the US does not want peace.”

“They want to weaken their rival Russia and say so quite openly,” he added.

Lafontaine, however, clarified that he condemns the war, “just like I condemn without any qualification all other wars that violate international law.”

The politician argued that further arms to Ukraine will prolong the war, meaning “yet more people will die.” He accused politicians in the West of thinking purely in the categories of ‘victory’ and ‘defeat,’ while ignoring the “most important” aspect, which is saving people’s lives.

According to Lafontaine, “those, who do not want more people to die, must be against any prolongation of the war, and consequently also against any weapons delivery.”

He criticized the argument that by providing military support to Kiev, the West is helping Ukraine defend itself, questioning why no one called for supporting “countries attacked by the US with deliveries of German weapons” in the past.

Speaking of Russia sanctions, Lafontaine claimed that they “are increasingly hurting people here at home – especially those with lower incomes, who can no longer pay their energy bills.”

“We are shooting ourselves in the knee. The US is probably laughing at us, because they are hardly affected by the sanctions, they can sell their liquefied natural gas in Europe in bigger quantities and their defense industry is getting a lot of business.”

The former SPD chair believes the current German leadership is in no position to work in the country’s own best interest, being nothing more than a “loyal vassal of the US.”

Lafontaine noted that the Green Party, which is part of the ruling coalition, has firmly entrenched itself in the role of the “extended arm of the US in the Bundestag” since the Yugoslav war. The party “supports every US decision when it comes to wars,” the politician said, adding that the Greens only pay attention to human rights violations when those happen in Russia or China.

The party’s current stance illustrates a radical transformation from a pacifist political force it once was. The Social Democratic Party, which the current Chancellor Olaf Scholz is a member of, too, has changed dramatically, according to its former chair, drifting away from its principles of peace, disarmament and social improvements.

Lafontaine reserved special criticism for the German press, which “is blind to the US war crimes” while offering a platform for warmongers.

The veteran German politician said that many in Germany feared that the “war will spread,” calling on the public to take to the streets in keeping with the tradition of the “peace movement of the 1980’s.”

May 22, 2022 Posted by | Militarism | , , , | 5 Comments

Australian Doctors Finally Speak Out! – Conference Of Conscience – Part 1

Zee Media | May 19, 2022

Over the past two years, no professional group has been silenced, threatened, or targeted more than Australian doctors. So many have stayed silent because of organisations such as AHPRA and various Medical Boards threatening to suspend or de-register them if they dare voice their genuine concerns as physicians.

For the first time in a conference of this nature, a group of brave Australian doctors have finally decided to speak out about what they and their patients have been subjected to, the ways the government and TGA have skewed the safety and efficacy data of the COVID-19 vaccines, purposeful suppression of early treatment that could have saved hundreds of thousands of lives, and the danger of continuing the COVID-19 vaccination program.

Australia and the whole world is currently at risk. The World Health Organization who is largely responsible for millions of deaths globally is currently proposing a global Pandemic Treaty which seeks to give the WHO complete control over every country. More information about this can be found on

Stay tuned for Part 2.

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May 22, 2022 Posted by | Science and Pseudo-Science, Timeless or most popular, Video | , , , | 2 Comments