Ex-Pentagon Analyst Doubts China Would Risk Sending Surveillance Balloon Over US
Sputnik – 04.02.2023
WASHINGTON – A former US defense official told Sputnik it is hard to imagine why China would risk sending an uncontrollable balloon with high-end surveillance equipment over the United States.
The Pentagon on Friday said it detected another Chinese surveillance balloon – this one transiting Latin America, which comes a day after the US identified the first one over Montana.
Beijing said the balloon over the US is a civilian airship intended for scientific research, however, Secretary of State Antony Blinken scrapped a high profile visit to China over the incident.
“It is hard to imagine why the Chinese would risk sending military-grade surveillance equipment in a vulnerable, uncontrollable balloon that cannot even be directed to a specific target,” former Pentagon analyst Chuck Spinney said. “These high altitude balloons basically go with the wind-flows.”
US constitutional historian and political commentator Dan Lazare said the US response has been a gross overreaction. Canceling an important diplomatic trip over something as trivial as this is absurd, he added.
China’s foreign ministry on Friday said the airship deviated far from its planned course and regrets the unintended entry into US airspace due to force majeure.
Merck’s Taxpayer-Subsidized COVID Pill Linked to New Virus Mutations, Study Finds
By Michael Nevradakis, Ph.D. | The Defender | February 3, 2023
Merck’s oral antiviral pill for COVID-19, molnupiravir — marketed under the name Lagevrio — may be fueling the development of new and potentially deadly variants of COVID-19, according to the authors of a new preprint study.
The study, released Jan. 27 by a team of U.S. and U.K researchers, found, “It is possible that some patients treated with molnupiravir might not fully clear SARS-CoV-2 infections, with the potential for onward transmission of molnupiravir-mutated viruses.”
Merck received significant taxpayer funding from the Biden administration to develop and distribute molnupiravir, and the U.S. government bought nearly 2 million courses of the drug on the taxpayer’s dime.
The study, which is pending peer review, followed the discovery by a middle school science and math teacher in Indiana who found numerous variants of COVID-19 emerged after molnupiravir began to be widely distributed.
Scientists had long warned that the development of such mutations from the use of molnupiravir was possible.
“It’s not a surprise that molnupiravir could cause [the] escape of mutant virus strains or substrains into the population,” said Dr. Harvey Risch. “Its main function is to get the virus to mutate faster.”
Risch, professor emeritus and senior research scientist in epidemiology (chronic diseases) at the Yale School of Public Health, told The Defender :
“The idea is that it will mutate itself to death. But some live mutants could get out, and this paper gives evidence that they have.”
Brian Hooker, Ph.D., P.E., chief scientific officer for Children’s Health Defense, said the study’s authors scanned global SARS-CoV-2 sequence databases looking for mutations characteristic of those by molnupiravir (G-to-A and C-to-U) and found an uptick of those mutants starting in 2022 — after molnupiravir was put on the market and specifically in countries where molnupiravir was distributed.
“Although this isn’t ‘direct proof’ that the mutations came directly from molnupiravir use,” Hooker told The Defender, “the evidence is very compelling, confirming the fears of many who warned of this prior to FDA [U.S. Food and Drug Administration] approval of the drug in late 2021.”
The FDA granted molnupiravir Emergency Use Authorization (EUA) on Dec. 23, 2021, for use in mild-to-moderate COVID-19 infections in patients 18 and over.
The EUA came just one day after the FDA authorized Pfizer’s COVID-19 antiviral treatment Paxlovid.
Merck this week announced massive revenues from sales of molnupiravir in 2022, but projected a significant decrease in those sales in 2023.
The FDA on Wednesday removed the requirement that a person has to test positive for COVID-19 in order to get a prescription for molnupiravir or Paxlovid.
‘I think we are courting disaster’
Molnupiravir “works by creating mutations in the COVID-19 genome that prevent the virus from replicating in the body, reducing the chances it will cause severe illness,” according to Bloomberg.
However, according to Science, the findings of the preprint study suggest “some people treated with the drug generate novel viruses that not only remain viable, but spread.”
This finding “underscores the risk of trying to intentionally alter the pathogen’s genetic code,” leading some researchers to “worry the drug may create more contagious or health-threatening variations of COVID,” Bloomberg reported.
Virologist William Haseltine, Ph.D., chair and president of ACCESS Health International, has repeatedly raised such concerns about molnupiravir.
“It’s very clear that viable mutant viruses can survive [molnupiravir treatment] and compete [with existing variants],” Haseltine told Science. “I think we are courting disaster.”
According to the Gateway Pundit, “When one studies how Lagevrio works, this should not come as a shock. The pill attacks the COVID virus by trying to alter its genetic code.”
The Gateway Pundit reported:
“Once inside a human cell, a virus can make 10,000 copies of its genetic code in a few hours. Each copy made increases the risk the virus makes a rare mistake and creates an inexact replica.
“This is how mutations happen as we have seen with COVID. A drug that deliberately alters a virus’s genetic code would greatly increase the mutation risk.”
Dr. Jonathan Li, a virologist and the director of Li Laboratory, associated with Harvard Medical School and Brigham and Women’s Hospital, told Bloomberg :
“There’s always been this underlying concern that it could contribute to a problem generating new variants. This has largely been hypothetical, but this preprint validates a lot of those concerns.”
According to Science, Haseltine and other scientists have long worried that molnupiravir would create COVID-19 mutations that “would survive and propagate — and perhaps turn out to be more transmissible or virulent than before.”
A Merck spokesperson described that theory as “an interesting hypothetical concern,” prior to the drug receiving EUA.
The same scientists also worried that aside from the virus, the DNA of those receiving the drug might also mutate, Science reported.
These concerns led “researchers and citizen scientists” to examine COVID-19 genome sequences cataloged in the international GISAID (Global Initiative on Sharing Avian Influenza Data) database, seeking to identify mutations likely to be caused by molnupiravir.
‘Clearly something is happening here’
Searching for these mutations was based on the premise that, “Rather than inducing random changes in the virus’ RNA genome, [molnupiravir] is more likely to cause specific nucleic acid substitutions, with guanine switching to adenine and cytosine to uracil,” added Science.
Through this process, Ryan Hisner, a middle school science and math teacher from Monroe, Indiana — described by Science as a “virus hunter” — ultimately “identified dozens of sequences that showed clusters of those hallmark substitutions.”
Hisner took to Twitter with his concerns, where he came into contact with Thomas Peacock, Ph.D., a virologist at the Imperial College London. They and other U.K. and U.S. researchers “systematically reviewed more than 13 million SARS-CoV-2 sequences in GISAID and analyzed those with clusters of more than 20 mutations,” according to Science.
The team found “a large subset showed the hallmark substitutions; all dated from 2022, after molnupiravir began to be widely used,” Science reported.
According to the preprint study, Molnupiravir, “acts by inducing mutations in the virus genome during replication. Most random mutations are likely to be deleterious to the virus, and many will be lethal.”
However, the researchers wrote:
“It is possible that some patients treated with molnupiravir might not fully clear SARS-CoV-2 infections, with the potential for onward transmission of molnupiravir-mutated viruses.
“We set out to systematically investigate global sequencing databases for a signature of molnupiravir mutagenesis. We find that a specific class of long phylogenetic branches appear almost exclusively in sequences from 2022, after the introduction of molnupiravir treatment, and in countries and age groups with widespread usage of the drug.
“Our data suggest a signature of molnupiravir mutagenesis can be seen in global sequencing databases, in some cases with onwards transmission.”
Peacock told Science these “signature clusters” were up to 100 times more likely to be identified in countries where molnupiravir was widely used, including the U.S., U.K. and Australia, as compared to countries such as Canada and France, where it was not in widespread use.
“Clearly something is happening here,” said Peacock.
Merck: ‘no evidence’ any antiviral agent has contributed to the emergence of circulating variants’
Theo Sanderson, Ph.D., a geneticist at the Francis Crick Institute and co-author of the preprint, told Science “We are not coming to a conclusion about risk” just yet, with regard to whether or not these mutations may lead to more severe COVID-19 variants.
Indeed, according to the preprint study, the variants identified by the researchers have not been shown to be more lethal or more evasive to immunity than other existing strains of COVID-19.
However, Haseltine illustrated the potential risk via the analogy of owning a pet lion: “Just because it didn’t bite you yesterday doesn’t mean it won’t bite you today.”
According to the Gateway Pundit :
“Merck was warned by multiple scientists their drug might create problematic mutations which would render the virus more dangerous and difficult to treat. The company decided to blow off any concerns and put Lagevrio [molnupiravir] on the market anyway.”
As previously reported by The Defender, Dr. James Hildreth, president and CEO of Meharry Medical College and member of Biden’s COVID-19 Health Equity Task Force, expressed concerns about mutant variants escaping.
In 2021, Hildreth told an FDA advisory panel, “Even if the probability is very low, one in 10,000 or 100,000, that this drug would induce an escape mutant from which the vaccines we have do not cover, that could be catastrophic for the whole world actually.”
Also in 2021, Haseltine told Science :
“You are putting a drug into circulation that is a potent mutagen at a time when we are deeply concerned about new variants. I can’t imagine doing anything more dangerous.
“If I were trying to create a new and more dangerous virus in humans, I would feed a subclinical dose [of molnupiravir] to people infected.”
Two other recent studies also called out molnupiravir, questioning its effectiveness and raising concerns the drug may help lead to the development of new COVID-19 variants.
A December 2022 preprint by a team of Australian researchers, found “this commonly used antiviral can ‘supercharge’ viral evolution in immunocompromised patients, potentially generating new variants and prolonging the pandemic.”
And a study published Jan. 28 in The Lancet found, “Molnupiravir did not reduce the frequency of COVID-19-associated hospitalisations or death among high-risk vaccinated adults in the community.”
University of Cambridge clinical microbiologist Ravindra Gupta, Ph.D., told Science that while it’s unclear whether molnupiravir will cause deadlier COVID-19 variants, the overall results of these recent studies “call into question whether molnupiravir should be used.”
Merck spokesperson Robert Josephson defended the product, telling Bloomberg, “There is no evidence that any antiviral agent has contributed to the emergence of circulating variants.”
Molnupiravir ‘different’ than Paxlovid — and ‘riskier’
Although molnupiravir is similar to Paxlovid in that both are oral antiviral treatments for COVID-19, Hooker told The Defender there are significant differences in how the two drugs work:
“Molnupiravir acts on the SARS-CoV-2 virus by directly inducing mutations in the RNA genome. This is a completely different mode of action compared to Pfizer’s product, Paxlovid, and in my estimation is quite dangerous.
“Merck claimed the mutation rate induced by molnupiravir would kill the virus and that mutants wouldn’t escape, but that has been shown to be false in studies of immunocompromised patients.”
Hooker said Paxlovid — and the COVID-19 vaccines — can potentially lead to the development of mutations as well.
But in his view, the “mechanism of action” used by molnupiravir is different — and far riskier — than Paxlovid and COVID-19 vaccines, which merely increase the virus’ lifetime in the human body, giving the virus a greater opportunity to naturally mutate.
Hooker said:
“In contrast, molnupiravir directly induces mutations and thereby vastly increases the mutation rate of the virus in the human host.
“In my estimation, this is a very dangerous way to treat such an infection, given the implications of creating random mutants.”
Merck made billions from molnupiravir — thanks to taxpayers
In 2022, sales of Merck’s molnupiravir hit $5.68 billion, fueled in part by strong fourth-quarter sales of the drug in Asia.
Fourth-quarter sales of molnupiravir reached $825 million, more than doubling analyst expectations of $358 million.
These strong earnings were boosted by government — or taxpayer — support.
In June 2021 — with molnupiravir still in clinical trials, which weren’t completed until October 2021 — the federal government signed a $1.2 billion contract with Merck for 1.7 million courses of the drug, at a cost of approximately $712 per patient.
An analysis by Melissa Barber of the Harvard T.H. Chan School of Public Health and Dzintars Gotham of King’s College Hospital in London found the cost of production of molnupiravir was approximately $1.74 per unit — or $17.74 for a five-day regimen.
By those calculations, the U.S. government paid a near-4,000% markup.
In March 2022, during his State of the Union address, President Biden announced the “Test to Treat” initiative, which allowed those who tested positive for COVID-19 at a pharmacy to obtain free antiviral pills — including molnupiravir — on the spot.
One month earlier, the Biden administration had proceeded with a new purchase of 3.1 million courses of molnupiravir, with the option to purchase more.
Estimates for Merck, and other COVID-19 drugmakers, are less rosy for 2023, as the public tires of all things pandemic and Biden looks to end the COVID-19 national emergency in May.
According to Reuters, sales of molnupiravir are expected to fall to about $1 billion this year, contributing to an expected decline in sales for Merck from $59.3 billion in 2022 to $57.2-$58.7 billion this year.
Merck’s stock price dropped by about 2% with Thursday’s announcement.
Despite these large earnings, overall sales of molnupiravir lagged significantly behind Paxlovid in 2022. Sales of Paxlovid reached $18.9 billion last year.
Michael Nevradakis, Ph.D., based in Athens, Greece, is a senior reporter for The Defender and part of the rotation of hosts for CHD.TV’s “Good Morning CHD.”
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
US giving cold feet to countries willing to normalize with Syria
Press TV – February 3, 2023
The United States is actively working to discourage countries willing to normalize relations with Syria, according to a report.
The report, based on the summary of a recent UN Security Council meeting on Syria seen by al-Akhbar, shows that Washington has tried to draw “red lines” for countries seeking to normalize with Syria, return the Syrian refugees to their homeland, or help find a permanent solution to the crisis in the Arab country.
Regarding the return of refugees, the report said instead of encouraging a repatriation process, the United States is urging the host countries to “double their support” for refugee programs, despite the heavy social and economic burden the refugee crisis puts on some of these countries, most notably Lebanon.
Al-Akhbar said the European representatives present in the meeting conditioned their support for the reconstruction of Syria and the repatriation of refugees on Damascus accepting a “credible and comprehensive political process” – which is considered by many to mean a political process dictated by Washington.
The report said that the summary of the meeting, which was held on January 25, shows the US-led camp continues to block a rapprochement – facilitated by Russia and Iran – between Syria and Turkey.
Ankara resumed diplomatic contacts with Damascus in late December, following a decade of severed ties in the wake of the crisis in Syria.
Turkey has now announced its willingness for a meeting between President Recep Tayyip Erdogan and his Syrian counterpart Bashar al-Assad.
A number of Arab countries have also resumed contact with Syria, including Oman and the United Arab Emirates.
Attempts by France & Germany to Negotiate With Russia Should Be Prevented, Bolton Tells Pranksters
By Andrei Dergalin – Sputnik – 02.02.2023
John Bolton shared his thoughts on topics such as the anti-Russian sanctions imposed by the West and the prospects of Ukraine’s NATO membership with Vovan and Lexus.
Former US presidential advisor John Bolton has made some rather frank admissions during a phone conversation with whom he thought was the ex-president of Ukraine, Petro Poroshenko.
Alas, his interlocutor turned out to be the well-known Russian prankster duo known as Vovan and Lexus, who promptly spilled the beans online.
During the chat, Bolton apparently insisted that all attempts by Germany or France to hold negotiations with Russia amid the current crisis in Ukraine should be disrupted, and claimed that the sooner Ukraine and Georgia become members of NATO, the better.
Regarding the sanctions imposed by western powers against Russia, Bolton complained that they weren’t enough and that Moscow continues to bypass these punitive measures.
He also commented on the promise made over three decades ago by former US Secretary of State James Baker to the former leader of the USSR Mikhail Gorbachev regarding NATO not expanding to the east, claiming that Baker merely “launched into arguments and looked for ways to avoid confrontation,” as the pranksters put it.
‘Türkiye and UAE told to cut trade ties with Russia’
RT | February 3, 2023
US officials have warned Türkiye and the United Arab Emirates against maintaining economic and financial ties with Russia because trade is undermining sanctions, Bloomberg reported on Friday, citing people with knowledge of the matter.
The warnings were reportedly voiced by the undersecretary for terrorism and financial intelligence at the US Treasury, Brian Nelson, during meetings with Turkish officials on Thursday and Friday.
Nelson’s visit to Türkiye comes as part of a regional tour that included the UAE earlier this week, and is said to be aimed at discussing Washington’s concerns over rising exports to Russia that include US goods.
US officials have called on the two countries to clamp down on the flow of goods to Russia, the sources told the news agency, adding that millions of dollars’ worth of export-controlled items were reaching the sanctions-hit country, and could be used by the defense industry to extend the conflict in Ukraine.
Scores of Turkish exporters shipped over $800 million worth of goods to Russia, including $300 million in machinery and another $80 million in electronics in the eight months through October 2022, according to people who spoke on condition of anonymity.
Other areas of concern reportedly include Russian vessels either sanctioned or subject to export controls making port calls in Turkey.
Meanwhile, the UAE has maintained ties with both Ukraine and Russia. The Gulf state’s ruler, Mohammed bin Zayed Al Nahyan, traveled to meet Russian President Vladimir Putin in October amid the continuing conflict in Ukraine. The leaders expressed Moscow and Abu Dhabi’s willingness to develop cooperation on all levels.
‘Nobody can tell us how to live’: Hungary slams US envoy for meddlesome remarks
“We welcome non-governors and non-regents”
Press TV – February 3 2023
Hungarian Foreign Minister Peter Szijjarto has lashed out at the US ambassador to Budapest for meddling in the country’s internal affairs over its support for Russia, saying, “Nobody can tell us from the outside how to live.”
Szijjarto issued the scathing rebuke on Thursday after David Pressman, who has represented Washington in Budapest since September last year, censured Hungary’s push for the continuation of policies endorsed by Russian President Vladimir Putin and the country’s opposition to Western-led anti-Russia sanctions over the conflict in Ukraine.
“Nobody can tell us from the outside how to live, so it is of no interest what a citizen of another country – be it an ambassador – thinks about the domestic political processes in Hungary,” Szijjarto said at a press conference. “We ask for more respect for the Hungarians, even from the ambassador.”
Stressing that it is not Pressman’s “job to interfere in the internal affairs of Hungary,” the Hungarian foreign minister said, “If he wants to use his stay in Hungary to qualify the activities of the government elected by the Hungarian people with a fairly clear majority… then he will have a very difficult time.”
Szijjarto said when Hungary receives foreign ambassadors, it expects them to behave appropriately and work to improve bilateral relations, emphasizing that the era of foreign envoys telling Hungarians how to live in their own country “is over.”
Hungary has on numerous occasions voiced opposition to Western sanctions against Moscow in response to Russia’s protracted military operation in Ukraine, arguing that the restrictions have wreaked havoc on the EU economy.
Last month, Hungarian Prime Minister Viktor Orban also slammed Germany’s decision to support Ukraine by supplying 14 Leopard 2 tanks, warning that such steps would make Western countries active participants in the conflict. Orban stressed that, instead of arming Kiev, the West should pursue “a ceasefire and peace talks” in Ukraine.
Russia launched what it calls a special military operation in Ukraine on February 24, 2022, over the perceived threat of the ex-Soviet republic joining NATO and to “de-Nazify” Kiev. Since then, the United States and Ukraine’s other allies have sent Kiev tens of billions of dollars’ worth of weapons, including rocket systems, drones, armored vehicles, tanks, and communication systems.
Western countries have also imposed a slew of economic sanctions on Moscow. The Kremlin has said the sanctions and the Western military assistance will only prolong the war.
Witness Forced to Walk Back Accusations That Led Maine Medical Board to Suspend Dr. Meryl Nass’ License
By Michael Nevradakis, Ph.D. | The Defender | February 1, 2023
The Maine Board of Licensure in Medicine on Tuesday held its third hearing on the suspension of Dr. Meryl Nass related to her treatment recommendations for patients with COVID-19.
As it did on day two of the hearings, held on Oct. 27, 2022, the board focused on Nass’ alleged “sloppy” record-keeping for three patients she treated and on her prescribing of ivermectin and hydroxychloroquine for those patients.
The board suspended Nass, a member of the Children’s Health Defense scientific advisory board, on Jan. 12, 2022, without a hearing.
The board initially accused Nass of “unprofessional” and “disruptive” behavior, spreading “misinformation” and prescribing hydroxychloroquine and a “deworming medication” (ivermectin) to patients.
However, the board withdrew the accusations of “misinformation” on Sept. 26, 2022, just prior to her first hearing date, Oct. 11, 2022.
The board’s case now rests on Nass’ alleged non-adherence to the medical “standard of care” as it pertained to ivermectin and hydroxychloroquine for treating COVID-19 and on the alleged “record-keeping” issues.
Two witnesses hired by the board — Dr. Thomas Courtney of the Maine Medical Center and Dr. Jeremy Samuel Faust, an emergency physician at Brigham and Women’s Hospital in Massachusetts and instructor at Harvard Medical School — testified during Tuesday’s proceedings, and Nass’ attorney, Gene Libby, cross-examined Courtney.
Cross-examination pokes holes in ‘expert witness’ testimony
Throughout his testimony, Courtney repeated his assertion that Nass did not follow an adequate standard of care in prescribing ivermectin and hydroxychloroquine to three patients, alleged improprieties in her communication and remote (telemedicine) consultations with the patients, and claimed Nass’ record-keeping was lacking.
But Courtney was obliged to walk back significant portions of his earlier testimony under his cross-examination by Libby.
For instance, Courtney claimed Nass did not adhere to an appropriate standard of care because she failed to advise two of her patients who didn’t recover as expected to seek care at an emergency room.
But under cross-examination, he acknowledged Nass had, in fact, advised the patients to go to the ER.
Courtney also criticized Nass for not prescribing monoclonal antibodies to her patients, one of whom was pregnant.
However, when cross-examined, Courtney admitted that, unlike hydroxychloroquine, monoclonal antibodies were not recommended for pregnant women and most monoclonal antibodies available at the time Nass was advising her patients were known to be ineffective against the Omicron variant of COVID-19, the dominant strain of the virus at that time.
Libby pointed out that the pregnant patient fully recovered eight days after the onset of her illness and had a normal birth, during which she was administered hydroxychloroquine and monoclonal antibodies.
Because evidence shows monoclonal antibodies are ineffective for pregnant women, the patient’s full recovery was credited to hydroxychloroquine.
Courtney also criticized Nass for making decisions about a patient’s care, including which medications to prescribe, on the basis of incomplete medical records.
He later walked back those claims after Libby demonstrated that Nass had received extensive documentation about the condition of one of the patients from his spouse, who provided Nass with vital signs, including the patient’s blood oxygen level.
Libby noted the three patients had specifically requested not to be treated with remdesivir, had asked to be prescribed ivermectin and hydroxychloroquine — and were fully within their rights as patients to request such treatment. Courtney was obliged to concur.
Libby also pointed out that off-label prescriptions of medications such as ivermectin and hydroxychloroquine, even for uses other than their primary purpose, are well within the generally accepted standard of care for physicians, and that federal agencies such as the U.S. Food and Drug Administration (FDA) and the National Institutes of Health do not issue binding requirements in this regard.
Courtney confirmed these statements.
In another characteristic exchange, Courtney, who had previously been critical of alleged gaps in Nass’s record keeping, was forced to concede that he did not “personally have a strong opinion on it.”
Referring to Courtney’s testimony, Nass wrote on her blog that despite his “opining that I lacked the fitness to practice medicine, he was unable to identify a single thing I had done wrong in my records.”
“I sent 2 patients to the ER when they did not recover as expected, although one of the board’s initial charges against me was that I failed to do so,” Nass wrote.
She likened the board’s accusations against her to “simply throwing lots of spaghetti on the wall to try and overwhelm me with charges so I would wilt and surrender my license.”
Referring to the medical claims Courtney made, Nass wrote:
“Courtney did not know the difference between an EUA [Emergency Use Authorization] product and a licensed drug. He incorrectly repeated a false claim made only once by FDA that the EUA for HCQ [hydroxychloroquine] was withdrawn because you would need to administer a toxic dose to get benefit. He had clearly failed to give that assertion any thought. Nor had he evaluated the U.S. government literature showing it to be false.
“He thought I should have treated 2 outpatients with monoclonal antibodies, but eventually agreed that cases in December 2021 were a mix of Omicron and Delta when the patients were ill, that none of their variants had been sequenced so we did not know which variant they had, and the monoclonals would not have worked against Omicron variants, which were likely to have been present then.”
“Doctor Courtney doesn’t read journal articles,” Nass wrote. “He sticks by the recommendations of government agencies and his specialty organization, the Infectious Diseases Society of America (IDSA).”
Nass noted that the IDSA was sued by the State of Connecticut “for denying the existence of chronic Lyme disease.”
In the brief time that was available for Faust to begin his testimony, he focused on attacking the credibility of Dr. Harvey Risch, an epidemiologist at the Yale University School of Public Health, for a journal article he wrote finding that treatments such as hydroxychloroquine were effective against COVID-19.
Nass had relied in part on Risch’s findings in dispensing hydroxychloroquine to her patients. During his testimony, Faust claimed, “There’s no disagreement here among the most prestigious experts in this area” with regard to the purported lack of effectiveness of hydroxychloroquine in treating COVID-19 patients.
Nass wrote:
“Faust was the Board’s epidemiology expert. He got some of the epidemiology right and he got a lot wrong. His arrogance when he was not sure of the answer was off-putting. He insulted Yale epidemiology professor Harvey Risch. He insulted my ability to read a journal article and he had a novel theory that this was sufficient disqualification to justify revoking my license.
“No one mentioned that Dr. Courtney could not cite journal articles used for forming his opinions on COVID treatment, having solely relied on pronouncements from government agencies.
“Should his license be revoked for that? Of course not.”
Nass also pointed out that Faust is a proponent of pregnant women receiving multiple mRNA injections. For instance, he was the lead author of “Pregnancy should be a condition eligible for additional doses of COVID-19 messenger RNA vaccines,” published in November 2022 in the American Journal of Obstetrics and Gynecology MFM.
Nass also wrote that Faust “publicly melted down when the mask mandate on planes was lifted,” accusing the Centers for Disease Control and Prevention of “killing babies.”
Next hearing set for March 2
The Maine board has scheduled two more hearings, the next one for March 2.
However, according to Nass, “The questioning of Dr. Faust is likely to take half a day more. Then I have 8 witnesses to go, including 3 patients who are at issue.”
About 140,000 people tuned in to Tuesday’s live broadcast of the proceedings, according to Nass.
Children’s Health Defense is providing support for Nass’ legal team.
Michael Nevradakis, Ph.D., based in Athens, Greece, is a senior reporter for The Defender and part of the rotation of hosts for CHD.TV’s “Good Morning CHD.”
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
California to Ditch Plans to Mandate COVID Vaccines for Schoolchildren
By Brenda Baletti, Ph.D. | The Defender | February 2, 2023
California will end plans to mandate COVID-19 vaccines for schoolchildren when the state ends its COVID-19 state of emergency on Feb. 28, California Department of Public Health officials told EdSource, which reported the news on Wednesday.
Commenting on the news, Michael Kane, national grassroots organizer for Children’s Health Defense (CHD) and founder of NY Teachers For Choice, told The Defender :
“We [in the movement] have some really good momentum right now, and what just happened in California is indicative of that.
“People are done with this. They’re done with the most extreme portions of this COVID agenda, the idea of this shot in kids is a no-starter for anybody.”
Gov. Gavin Newsom announced in October 2021, that California would be the first state to require COVID-19 vaccinations for children to attend school. It was also the first to mandate masking and staff vaccination measures.
At the time, state Sen. Richard Pan proposed legislation to strengthen the vaccine requirement even further by eliminating personal and religious exemptions. The legislation didn’t pass.
The vaccine requirement for children was originally set to kick in on July 1, 2022, when it was expected the vaccines, still under Emergency Use Authorization at the time, would be fully approved by the U.S. Food and Drug Administration (FDA).
But in April 2022, California announced it would delay the mandate to July 1, 2023.
The FDA still has not fully approved the COVID-19 vaccines for anyone under age 12. The CDC recommends the vaccines and the bivalent boosters for children ages 6 months and older.
The bivalent boosters were authorized for emergency use without any human clinical trials.
In California, 67% of 12- to 17-year-olds and 38% of children ages 5 to 11 have received two doses of the COVID-19 vaccine primary series. Less than 42% of 12- to 17-year-olds and less than 30% of 5- to 11-year-olds have been boosted.
Those numbers are higher than national averages. Only 58% of children ages 12 to 17 and 32% of children ages 5 to 11 have received two doses of the vaccine.
“The booster uptake is a complete failure, so this idea of routinizing a COVID shot for school every year, which is what they wanted, is failing in all the states they thought it was a guarantee in,” Kane said.
California ended the school mask mandate in March 2022, and ended the vaccine mandate for teachers and school staff in October 2022.
‘This kind of coercion never should have been normalized’
In the last two years, while state lawmakers debated California’s school vaccine mandate, school districts across the state proposed and passed their own COVID-19 vaccine mandates.
Alex Gutentag, former Oakland public school teacher and political analyst, told The Defender :
“Newsom has referred to California as ‘the true freedom state,’ but he more than any other U.S. governor has tried to undermine the medical freedom of kids and their families when it comes to COVID-19.
“It is definitely a positive development that California is ending its plan for a school mandate, but it’s important to remember that many kids have already been coerced into vaccination through the threat of both statewide and local mandates.
“Several California cities, including Los Angeles, told families that COVID vaccines would be required to attend school in person, but eventually had to scrap and delay these plans. It was a clear effort to increase vaccine uptake, and was a major abuse of power. This kind of coercion never should have been normalized.”
The pressure to scrap mandate plans came in part from attorneys and citizen advocacy groups who brought three major lawsuits against the Los Angeles Unified School District (LAUSD), the Piedmont Unified School District and the San Diego Unified School District (SDUSD).
Children’s Health Defense-California Chapter (CHD-CA) and Protection of the Educational Rights of Kids (PERK), a California-based child advocacy group, used state laws to rule out local policies and pause vaccine mandates in the LAUSD and the Piedmont school district.
They sued the LAUSD, the second-largest school district in the U.S., alleging the district lacked the legal authority to impose a COVID-19 vaccine requirement for students ages 12 and older.
The mandate would have excluded 32,000 students from in-person classes.
After Judge Mitchell L. Beckloff ruled the case could go forward in April 2022, the LAUSD announced it would delay the COVID-19 vaccine requirement until July 1, when the state mandate kicked in.
Piedmont also voted to repeal its mandate after a judge granted CHD-CA and PERK’s Application for an Alternative Writ of Mandate and ordered the district to show why its policy could not be struck down.
In San Diego, a group called Let Them Choose filed a lawsuit contesting the SDUSD’s vaccine mandate for school children ages 16 and up. The court ruled, and in December 2022, an appellate court affirmed, that the district’s mandate violated state guidelines.
According to Rita Barnett-Rose, legal director of CHD-CA, the San Diego ruling established that individual school districts cannot institute COVID-19 vaccine mandates at the district level, because there is a statewide statutory scheme in place to set mandates.
That means the end of the California COVID-19 vaccine mandate for children at the state level will effectively end all school mandates in California.
Political will for mandates faltering across the country
Rita Barnett-Rose underscored that California health officials have not yet made the news about ending the mandate for the state’s schools official. However, she said, “Right now it looks like positive news.”
However, Barnett-Rose said, “The question still remains, are they [state legislature] going to try to put something on the legislative agenda this year?”
Gutentag also noted the lack of an official announcement:
“I also think it’s notable that officials only said they were not going to implement the mandate after EdSource pressed them for answers. State leaders probably knew that there were too many legal and logistical challenges, but did not want to admit this in order to save face.
“All Californians should be concerned that our state government is not honest and direct with us about major policy decisions.”
This shift in California’s school mandate decision is the latest in a string of developments calling into question the COVID-19 vaccines and marking a shift in public consensus on vaccines.
“I’m not surprised at all that California is admitting that it’s not politically possible to force a shot that’s unnecessary and dangerous on children to attend school,” Kane said, adding:
“It makes perfect sense to me, given what I am seeing in New York that this same type of pressure is in California.
“The entire thing is political. The whole thing is what can we politically do? They can’t politically force the shot on kids. The fallout is too much. They just can’t risk it, you know.”
Barnett-Rose told The Defender she thinks that when Newsom announced the mandate he thought a lot of other states would follow suit.
“I’m hoping this signifies that the political will to force these mandates on kids is really declining significantly.”
CDC adds COVID shots to child immunization schedule
California reversed its vaccine mandate decision despite the fact that in October 2022, the Centers for Disease Control and Prevention recommended adding COVID-19 vaccines for children as young as 6 months old to the new Child and Adolescent Immunization Schedule, which will be rolled out this month.
The revised recommendations include the Moderna or Pfizer-BioNTech COVID-19 vaccine for children as young as 6 months and the Novavax COVID-19 vaccine for children as young as 12 years.
All COVID-19 vaccines being administered in the U.S. to people under 18 are still Emergency Use Authorized (EUA) products.
The FDA did grant full approval to Pfizer’s Comirnaty COVID-19 vaccine for ages 12 and older. However, the Comirnaty vaccine is not available in the U.S. — which means all children who get the Pfizer vaccine are getting an EUA product.
The FDA also informed a congressional committee in May 2022 that the COVID-19 vaccines for children under 6 would not have to meet the agency’s 50% efficacy threshold required to obtain EUA.
COVID-19 vaccines for adolescents, teens and adults had to meet the requirement.
“If these vaccines seem to be mirroring efficacy in adults and just seem to be less effective against Omicron like they are for adults, we will probably still authorize,” Peter Marks, M.D., Ph.D., director of the Center for Biologics Evaluation and Research at the FDA, told the House Select Subcommittee on the Coronavirus Crisis.
Last week, The Epoch Times reported that recently released emails revealed top officials, including Marks, rushed approval of Pfizer’s COVID-19 vaccine to enable vaccine mandates, despite concern by others in the agency that the rush compromised the integrity of the approval process.
On Dec. 9, 2022, the CDC expanded the use of updated (bivalent) COVID-19 vaccines for children ages 6 months through 5 years. They made that decision despite the fact that the bivalent shots were approved for adults without any clinical data and have yet to show efficacy.
In an amicus brief for a lawsuit challenging the vaccine mandate for school children in the state of Louisiana, CHD wrote:
“Simply put, the COVID vaccines have not been shown to be either effective or safe for children. The benefits to children are minuscule, while the risks — including the risk of potentially fatal heart damage — are ‘known’ and ‘serious,’ as the [FDA] itself has acknowledged.”
The Louisiana Department of Health rescinded the mandate.
Legal struggles continue over age of consent for vaccines
Legal battles over vaccines for children in California and elsewhere are ongoing.
In California, Maribel Duarte is suing the LAUSD and Barack Obama Global Preparation Academy alleging they vaccinated her 13-year-old son without her consent.
A vaccine clinic was set up in his school — Barack Obama Global Prep Academy — and he was allegedly bribed with a pizza to get vaccinated without parental consent.
One of the adults at the clinic requested the teen provide a parent-signed consent form, which he did not have. The child was then told to sign his mother’s name and not tell anyone.
Currently, Sen. Cheryl Kagen of Maryland is proposing Senate Bill 378, which would allow children 14 and up to consent to vaccination themselves and prevent parents from accessing medical records.
California attempted to pass a similar bill, SB 866, for children ages 12 and up.
The District of Columbia also attempted to pass a similar law, for children 11 and older, but a preliminary injunction issued in March 2022 temporarily blocked the district from implementing the law.
CHD and the Parental Rights Foundation sued the district and are seeking to declare the D.C. act unconstitutional.
The D.C. school district still plans to mandate children be vaccinated against COVID-19 to attend school starting in the 2023-2024 school year, just not without their parents’ consent.
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
NYT: Covid Vaccine Makers and Bill Gates’ GAVI Screwed Everyone
US Government and Other Governments are Holding The Bag
By Igor Chudov | February 1, 2023
This New York Times story from today is very illustrative of the current times.
Vaccine Makers Kept $1.4 Billion in Prepayments for Canceled Covid Shots for the World’s Poor
Separately, Johnson & Johnson is demanding additional payment for unwanted shots, confidential documents show.
It turns out that makers of Covid vaccines expertly screwed their customers, keeping a large part of the prepayment money advanced to them without shipping vaccine doses that no longer find any demand.
As global demand for Covid-19 vaccines dries up, the program responsible for vaccinating the world’s poor has been urgently negotiating to try to get out of its deals with pharmaceutical companies for shots it no longer needs.
Drug companies have so far declined to refund $1.4 billion in advance payments for now-canceled doses, according to confidential documents obtained by The New York Times.
The worst example is J&J, manufacturer of the Janssen vaccine, which was pulled from use worldwide due to blood clots. Despite that, J&J demands that more money be given to it “because of existing contracts.”
If it cannot strike a more favorable agreement with another company, Johnson & Johnson, it could have to pay still more.
Gavi and Johnson & Johnson are locked in a bitter dispute over payment for shots that Gavi told the company months ago it would not need, but which the company produced anyway. Johnson & Johnson is now demanding that Gavi pay an additional, undisclosed amount for them.
New York Times is lamenting this situation and highlights appeals to the conscience of vaccine makers:
Covid vaccine manufacturers “have a special responsibility” because their products are a societal good and most were developed with public funding, said Thomas Frieden, the chief executive of the global health nonprofit Resolve to Save Lives and a former director of the United States Centers for Disease Control and Prevention.
Who is Thomas Frieden? He is a former director of the CDC and also a convicted sex offender, in my opinion.
Vaccine makers resist Frieden’s appeals to their conscience because they do not have any.
Bill Gates’ GAVI is not asking Pfizer for refunds: Pfizer was paid directly by the US government. Did Bill Gates pull strings to have the US government hold the financial bag in the case of Pfizer?
If so, Bill certainly had personal financial reasons for this!
Bill and Melinda Gates Foundation invested 55 million into Pfizer’s vaccine maker BioNTech in Sep 2019.
This investment was made when BioNTech was an obscure company with no vaccines in the pipeline. That “unexpectedly” changed mere months later when BioNTech was selected to become the largest producer of Covid vaccines. Such lucky timing for Bill!
So, Bill Gates, having a financial interest in BioNTech, did not want his own GAVI to pay for BioNTech vaccines that eventually found no buyer; instead, the US government paid Pfizer directly. Pfizer will keep the funds, giving the US government an “option” to buy vaccines that nobody wants anymore.
Under the revised deal, a total of 600 million Pfizer doses will be made available to the US by the end of the year, giving the administration more time to find countries who want them. Pfizer had originally agreed to sell a billion shots at cost by this month.
Bill Gates-funded GAVI seems to have screwed its donors innovatively: the donors gave money towards Covid vaccinations, which fizzled. Hence, GAVI received back 1.6 billion out of 2.3 donated billions it gave Covid vaccine makers. Gavi, however, will not refund 1.6 billion to the donors and will use the money it recovered for other purposes, inflating its budget:
Had some vaccine manufacturers not been willing to renegotiate their contracts with Gavi, the costs to the organization could have been much higher. Gavi would have been on the hook for $2.3 billion for the doses it wanted to cancel, the documents show, but it saved $1.6 billion by exiting those contracts.
…
Donations for Covid shots substantially inflated Gavi’s budget, and the lost prepayments for canceled Covid vaccines do not threaten its regular childhood-vaccination work.
Such is the current state of the pandemic. The money is gone; vaccines do not work; people are dying suddenly; the government and Big Pharma do not want the public to pay attention.
If you, my reader, are in the United States, remember that the US government’s money is your money. Say bye-bye to it.
Will there be any real investigations?
Federal government is accused of using antiterrorism tech to target vaccine dissent
Using it against its own citizens
By Ken Macon | Reclaim The Net | February 2, 2023
The US federal government is adopting military-grade AI that was used to crack down on ISIS to censor dissent by US citizens on issues like election fraud and vaccine hesitancy, according to the executive director of the Foundation for Freedom Online, Mike Benz.
Private firms and universities have received millions of dollars in grants from the National Science Foundation (NSF), a federal agency, to develop tools similar to those developed by the Defense Advanced Research Projects Agency’s Social Media in Strategic Communications (SMISC) program in 2011.
SMISC’s tools were used “to help identify misinformation or deception campaigns and counter them with truthful information,” in the Middle East. In a report, Mike Benz detailed how the NSF and other organizations are using this technology to censor the speech of Americans.
“One of the most disturbing aspects of the Convergence Accelerator Track F domestic censorship projects is how similar they are to military-grade social media network censorship and monitoring tools developed by the Pentagon for the counterinsurgency and counterterrorism contexts abroad,” reads the report.
Speaking to Just the News, he said: “DARPA’s been funding an AI network using the science of social media mapping dating back to at least 2011-2012, during the Arab Spring abroad and during the Occupy Wall Street movement here at home. They then bolstered it during the time of ISIS to identify homegrown ISIS threats in 2014-2015.”
According to Benz, the NSF has adopted DARPA’s technology to target two groups of Americans: those skeptical of recent election results and those who claim COVID-19 vaccines could be harmful.
“The terrifying thing is, as all of this played out, it was redirected inward during 2016 — domestic populism was treated as a foreign national security threat,” Benz said.
“What you’ve seen is a grafting on of these concepts of mis- and disinformation that were escalated to such high-intensity levels in the news over the past several years being converted into a tangible, formal government program to fund and accelerate the science of censorship,” he said.
“You had this project at the National Science Foundation called the Convergence Accelerator,” Benz recounted, “which was created by the Trump administration to tackle grand challenges like quantum technology. When the Biden administration came to power, they basically took this infrastructure for multidisciplinary science work to converge on a common science problem and took the problem of what people say on social media as being on the level of, say, quantum technology.
“And so they created a new track called the track F program … and it’s for ‘trust and authenticity,’ but what that means is, and what it’s a code word for is, if trust in the government or trust in the media cannot be earned, it must be installed. And so they are funding artificial intelligence, censorship capacities, to censor people who distrust government or media.”
Benz noted how mainstream media and fact-checkers have become arbiters of truth, determining what is acceptable and unacceptable to post online, and how the pandemic has normalized “censorship in the name of public health.”
“What’s happened now is the government says, ‘Okay, we’ve established this normative foothold in it being okay to [censor political speech], now we’re going to supercharge you guys with all sorts of DARPA military grade censorship, weaponry, so that you can now take what you’ve achieved in the censorship space and scale it to the level of a U.S. counterinsurgency operation,’” Benz explained.
George Soros is either prophetic or pulls a lot of strings
By Tony Cox | RT | February 2, 2023
George Soros is either stunningly prescient or frighteningly influential when it comes to determining who will need to do all the bleeding and dying that he deems necessary to bring about a desirable “new world order.”
Consider the Hungarian-born billionaire’s essay on the future of NATO: “The United States would not be called upon to act as the policeman of the world. When it acts, it would act in conjunction with others. Incidentally, the combination of manpower from Eastern Europe with the technical capabilities of NATO would greatly enhance the military potential of the partnership because it would reduce the risk of body bags for NATO countries, which is the main constraint on their willingness to act. This is a viable alternative to the looming world disorder.”
Soros deserves credit for neatly describing the US and NATO strategy for bringing about and exploiting the Russia-Ukraine conflict. The Ukrainians are providing the manpower – in other words, the cannon fodder – and the Western puppeteers can endeavor to weaken Russia and enforce their vision of a favorable world order. They also can do this without having to make the case to their citizens that this is a fight for which it is worth tolerating body bags coming home from the front.
Additionally, by sharing the burden of providing military and economic aid to Kiev, the Western powers achieve the dual benefits of prolonging their proxy war and creating the impression that the whole world is steadfastly standing with the blue and yellow. That helps underpin the narrative frame that there is no moral basis for criticizing Ukraine policy and anyone who does so is probably a Kremlin agent.
The thing is, Soros didn’t write his take on the situation this week, this month or even in the past year. He didn’t even write it back in 2014, when he was allegedly backing the overthrow of Ukraine’s elected government and might have reasonably anticipated a coming conflict with Russia. No, Soros wrote this assessment in 1993, nearly 30 years ago.
Back then, in the wake of the Soviet Union’s collapse, Soros wanted to prevent former Soviet states and Warsaw Pact nations from becoming nationalist countries that would be governed according to their own interests and oppose the global order that he was promoting.
Western leaders had made assurances that NATO wouldn’t expand eastward, but Soros saw the military bloc as “the basis of a new world order.” He conceded that the group would need “some profound new thinking,” given that its original mission was “obsolete,” and he insisted that the alliance must be free to invite any country to join.
In fact, he saw a great opportunity for NATO to take advantage of the security void created by the Soviet collapse if it could act quickly. “If NATO has any mission at all, it is to project its power and influence into the region, and the mission is best defined in terms of open and closed societies.”
“The countries of Central Europe are clamoring for full membership of NATO as soon as possible, preferably before Russia recovers. Russia objects, not because it harbors any designs on its former empire but because it sees no advantage in consenting. Its national pride has been hurt and it is sick and tired of making concessions without corresponding benefits.”
Soros saw NATO as both a viable platform to develop into the anti-Russia enforcer for his new world order and the bright and shiny object to lure Europe’s former Eastern Bloc states into the fold. “NATO has a unified command structure which brings together the United States and Western Europe,” he said.
“There are great advantages in having such a strong Western pillar: It leads to a lopsided structure firmly rooted in the West. This is as it should be, since the goal is to reinforce and gratify the desire of the region for joining the open society of the West.”
The goal became reality. For example, Soros noted that there was nothing to prevent countries such as Poland, Czechia and Hungary from joining NATO. The three nations became the first wave of NATO’s post-Cold War expansion, joining the bloc in 1999. In fact, the bloc has since nearly doubled in size, adding 14 members by 2020 and teeing up Ukraine and Georgia as future prospects.
NATO moved right along the Russian frontier, placing strategic weapons and security guarantees on Moscow’s doorstep and helping to trigger the current crisis. As Soros acknowledged in 1993, Russia had no desire to restore the empire of Peter the Great – contrary to a popular CNN talking point. However, as the Kremlin warned repeatedly in the years leading up to the current conflict, Moscow couldn’t stand idly by while its national security interests were trampled.
It’s easy to see why Soros was and is so worried about nationalism: His vision could never sell with a government that served the interests of its own people.
NATO’s expansion binge didn’t make anyone safer. We know the little brothers, like the people of Ukraine, aren’t better off. They have the privilege of bleeding and dying as they provide the “manpower” for NATO’s proxy fight with Russia. As for the big brothers, they undermine their own security. Americans and Western Europeans are suffering the economic effects of the US-NATO sanctions war against Russia, and their governments are pushing them ever closer to a planet-ending nuclear Armageddon.
The Bulletin of the Atomic Scientists announced last week that its Doomsday Clock had advanced to within 90 seconds of midnight, the latest ever, indicating that humanity stands at “a time of unprecedented danger.” The group cited the Russia-Ukraine conflict, which has “challenged the nuclear order – the system of agreements and understandings that have been constructed over six decades to limit the dangers of nuclear weapons.”
Not to worry if you’re George Soros, 92 years old, and watching your geopolitical dreams come true. He and others like him can keep marching onward to perfect their world order as they see fit.
If we wonder whether NATO works on behalf of that order, we need look only at what has transpired and the framing of the current conflict. When Russian forces began their offensive against Ukraine last February, Western leaders and pundits condemned President Vladimir Putin for undermining the “rules-based international order.”
So NATO has emerged as the enforcer of the rules-based international order – the new world order, if you will – just as Soros called for three decades ago. The results of that “profound new thinking” are much the same as the political activist envisioned in 1993. He also called for expanding NATO to Asia, which hasn’t yet happened, but the bloc’s 2022 summit was enlarged to include representatives from Asia-Pacific “sentinel states” – Japan, South Korea, Australia and New Zealand.
Was Soros so much of a visionary that the hedge-fund investor could foresee how geopolitics would play out several decades ahead of time, or does his accuracy reflect the fact that he and his allies tend to get their way? Rather than prescience, is this situation more like the cook being a good predictor of what we’re going to have for dinner?
Soros himself offered a hint on that theory in his essay: “We have to act without full knowledge of the facts because the facts are created by our decisions.”
Anyone who suggests that Soros calls a lot of the policy shots is immediately condemned by the Western media as anti-Semitic because, after all, he has Jewish heritage. Never mind that he’s an avowed atheist who has been accused of undermining Israel’s democratically elected government and funding groups that defame the Jewish state.
So when Moldovan President Maia Sandu returns from a recent trip to Davos and promptly starts hinting about joining NATO – in violation of her country’s constitutional commitment to neutrality – we shouldn’t point out that she met with Alexander Soros, son of George Soros, during the summit. Revealing or trying to connect such dots would be anti-Semitic, according to the Western media.
It couldn’t be that George Soros wields an inordinate amount of influence over world affairs. It couldn’t be that some of his critics have legitimate and unbigoted disagreements with his ideas. It couldn’t be that his immunity to criticism is further evidence of his power.
And shut your eyes when a US watchdog group reveals that Soros has financial ties to at least 253 media organizations worldwide and funding links to 54 prominent media figures, including such names as Christiane Amanpour of CNN, Lester Holt of NBC News and Washington Post executive editor Sally Buzbee.
So Soros gets to wield his influence with impunity, apparently achieving what he wants in many cases. He gets to serve the interests of billionaires, defense contractors, power-mongering politicians and social engineers. But what about the rest of us, the other 8 billion people in the world? What about those who just want to be able to support our families, pursue happiness and live in peace – without worrying that iodine pills are sold out and there might not be time to build a nuclear fallout shelter?
Soros himself might prescribe us more bread and circuses, to keep the masses distracted – as well as tribalism, to keep the people divided – at least until we’re needed to serve as “manpower” for the cause.
Tony Cox is a US journalist who has written or edited for Bloomberg and several major daily newspapers.
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From the Archives
Israel: Strategic Ally or Liability?
By Stephen Sniegoski | My Catbird Seat | June 12, 2010
The claim that Israel serves as a valuable ally for the United States is made by both pro-Zionists and much of the anti-war and anti-Zionist Left that is influenced by Noam Chomsky. As a result of the Gaza flotilla massacre, which has caused a world-wide uproar against Israel, the value of Israel to the United States is being publicly questioned in more mainstream foreign policy forums. … continue
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