On the morning of January 25, 1993, a man named Mir Amal Kansi appeared outside CIA headquarters in Langley, Virginia, where he began assassinating people who were driving their cars into the facility. He ended up killing two CIA employees and wounding three others.
Four years later, FBI agents arrested Kansi in Pakistan and brought him back to the United States.
Kansi was prosecuted in a Virginia state court for murder, where he was convicted and sentenced to die. On November 14, 2002, the state of Virginia executed him.
What I find fascinating in this episode is that under U.S national-security law, when the CIA assassinates people, it isn’t considered murder. But as Kansi’s case shows, when people assassinate CIA officials, it is considered murder.
Kansi gave the reason for his assassinations. No, he didn’t say that he hated America for its “freedom and values.” He said that the reason he was assassinating CIA officials was to retaliate for the fact that the U.S. government was killing people in Iraq and for its role in helping Israel kill Palestinians.
Under U.S. national-security law, U.S. officials can assassinate anyone they want — “communists,” “terrorists,” “bad guys,” “adversaries,” “opponents,” “rivals,” or “enemies.” When they do that, it’s to be called an “assassination” or a “targeted killing.”
Moreover, under the law, U.S. officials can kill whoever they want with economic sanctions, as they were doing with the Iraqi people at the time that Kansi was retaliating. I am reminded of U.S. Ambassador Madeleine Albright’s infamous statement that the deaths of half-a-million Iraqi children from the sanctions were “worth it.” Those killings weren’t called “murder” of course. They were called unfortunate deaths arising from the sanctions.
U.S. officials also wield the authority to kill whoever they want with invasions of Third-World countries. The people of Afghanistan and Iraq can attest to that. Again, those killings are not considered to be murder. They are considered to be casualties of war.
If, however, anyone retaliates against the national-security establishment by assassinating officials within the national-security establishment, it’s called “murder,” in which case the assassin will be put to death after being accorded a trial.
Of course, this was the law prior to the 9/11 attacks. After those attacks, the law was implicitly amended to provide that the national-security establishment had the option of taking “bad guys” like Kansi to Gitmo, where they could be tortured, held indefinitely without trial, or executed after a kangaroo trial before a military tribunal.
All this hypocrisy goes to show what the conversion from a limited-government republic to a national-security state has done to the consciences of the American people. Most everyone has come to accept the state-sponsored assassinations and deaths arising from sanctions, embargoes, invasions, occupations, and wars of aggression to just be part of the U.S. government’s “foreign policy tools.”
As I pointed out in a recent blog post, however, the Pentagon’s and the CIA’s assassinations constitute murder, just as Kansi’s assassinations do. Why, even Lyndon Johnson referred to the CIA’s assassination program as “Murder, Inc.,” which is precisely what it is. The same goes for deaths arising from sanctions, embargoes, wars of aggression, invasions, and occupations. It’s just plain murder.
Referring to Kansi, Virginia prosecutor Robert F. Horne stated, “I’ve tried an awful lot of killers in my life, and I think he’s the only one I’ve run into that is absolutely proud of what he did. You get a lot of killers who don’t feel all that bad about what they did, but he’s proud of it.”
Apparently Horne has never met any CIA assassins. Like Kansi, they feel really good about their killings and are absolutely proud of what they do. What Horne fails to realize is that even though Kansi is a “bad guy” for assassinating people, that doesn’t convert the CIA assassins into “good guys.”
It’s probably worth mentioning that after Kansi was executed, four American citizens were assassinated in Pakistan in retaliation.
What we need in America is a great awakening, one that involves a revival of individual conscience. When that day comes, Americans will put a stop to the evil within our midst by converting America back to a limited-government republic and putting an end to state-sponsored murder. It will also make Americans traveling overseas a lot safer.
February 9, 2022
Posted by aletho |
Militarism, Progressive Hypocrite, Timeless or most popular, War Crimes, Wars for Israel | CIA, Human rights, Iraq, Palestine, United States |
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Attention has increasingly begun to turn towards vaccine efficacy and vaccine damage now that we have collated some twelve months of data. HART has recently focused on the issue of the appropriateness and efficacy, as well as safety, of vaccinating children. One of the issues that has not been explored by anyone is liability for vaccine-induced damage; by this is meant liability to those not covered by the blanket government indemnity given to the vaccine manufacturers, but the potential liability of those pushing the vaccines, be that the personal liability of government officials, NHS employees, schools as well as public and private sector employers (or potentially the officials and employees of these organisations themselves). This is a real issue given that none of the individuals encouraging, administering or in other ways nudging or coercing the acceptance of these procedures has any idea of the content of the vaccines, nor of the medium or long term side effects that these might produce.
This article was prompted by an unconfirmed report (court papers have not been published so as far as we are concerned this remains anecdotal) from France that a life insurance company had refused a claim under its policy against the death of an insured individual who died of the vaccine. The refusal was justified on the basis that damage from experimental voluntary medical procedures are not covered (the vaccines are currently still of course only approved under an emergency protocol) and that such a death would therefore be classified as suicide. It went on to say that suicide from this cause was also not covered under its policy. The case was taken to the highest court in France and the claimants lost. It is not clear that an English court, for a similar situation in England and Wales under English law, would come to the same conclusion. The view from discussions in the insurance market is that it would not, but this is also anecdotal at this stage. Suicide would almost invariably be covered under an English law life insurance policy. However, the French case does begin to put this issue into sharper relief.
There have also been reports from an insurer in the United States (OneAmerica) that deaths of 16-64 year olds have increased by 40%, based on its numbers in comparable quarters year on year. Similar increases have been reported by the Insurance Regulatory and Development Authority of India. This is a catastrophic increase, given that a 1-in-200-year event would correspond to a 10% increase and would in itself be categorised as a catastrophe event by insurers if it were widely experienced. While one or two swallows does not make a summer, this is an unfolding event that insurers and regulators will be watching closely. The time to watch is this month as insurers begin to report on their Q4/21 numbers, but the picture is not likely to improve throughout the year. Swiss Re and Munich Re, the world’s most prolific reinsurers, will be worth keeping an eye on, as a key market bellwether. If the numbers are half or even a quarter as bad as OneAmerica’s data, there will have been some actuarial deep dives and the focus will soon turn to begin investigation of the vaccine as one of the only materially different exogenous factors that could have influenced the data.
Furthermore, one of the states of the USA is in the early stages of introducing primary legislation to make employers liable for just this sort of event. The US is notoriously litigious, though Canada and Australia are very close behind. The principle of requiring the manufacturer and in some cases distributor as well as in this instance the administrator of a product to be liable if it causes harm is a perfectly sound one. This ultimately would be for the courts to decide, but in a liability policy, all parties involved with the drug that does harm would be in the chain of people to sue. However, in the case of vaccinations, a key part of that principle has long been abandoned, in that for decades now, since the first Reagan administration and Thatcher’s era in the UK, governments have given full indemnities to the pharmaceutical industry for vaccine-related liabilities. Yet governments themselves offer only paltry and complex compensation schemes that can take years to pay out at huge actual, as well as emotional cost to the victims, for sums that come nowhere close to being real compensation. This is and always has been unjust, legally unwise and morally wrong. It effectively encourages the wrong priorities for pharma, giving profit an easy priority over safety. And worst of all, it leaves victims powerless, jobless, and of course injured. It puts them and their wider families into crippling financial difficulties and does nothing to curb the behaviour of pharma. The family speaking here describe the huge financial impact in addition to the impact of the injury itself on an 18-year-old girl and her parents. Add to that, cooperative governments that then mandate vaccines and encourage or coerce employers to do so. This is disproportionate given the risk from the virus in most younger people and we witness a healthcare system that seems to have become prone to forget — or even relegate — what should be a sacrosanct principle of First Do No Harm. The result is a toxic mix in which the only beneficiaries are the balance sheets of pharma and their shareholders.
One sure-fire way of stopping vaccine mandates in their tracks is for primary legislation to ensure that employers are liable if they go along with government mandates or nudges. Insurers are likely to react by reviewing coverage for such scenarios, where under legislation they can. Employers will not wish to assume such liabilities without adequate insurance. And should they fall foul of this obvious pitfall, shareholders may resort to Director’s and Officer’s liability insurance lawsuits before which Workers’ Compensation (and their European and other-world equivalents) actions are likely to play out.
Let us hope that such legislation passes and spreads swiftly around the world.
February 9, 2022
Posted by aletho |
Timeless or most popular, War Crimes | COVID-19 Vaccine, France, UK, United States |
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A succession of events in recent weeks all point to the inescapable fact that nearly 75 years of Israel’s painstaking efforts to hide the truth about its origins and its racist apartheid regime are failing miserably. The world is finally waking up, and Israel is losing ground quicker than it is able to gain new supporters or whitewash its past and ongoing crimes.
First, there were the revelations about Tantura, a peaceful Palestinian village whose inhabitants were mostly exterminated by Israel’s Alexandroni Brigade on 23 May, 1948. Like many other massacres committed against unarmed Palestinians over the years, the Tantura massacre was mostly remembered by the village’s few survivors, ordinary Palestinians and Palestinian historians. The mere attempt in 1998 by Israeli graduate student Theodore Katz to shed light on that bloody event ignited a legal, media and academic war, forcing him to retract his findings.
In a recent social media post, Professor Ilan Pappé revealed why, in 2007, he had to resign his position at Haifa University. “One of my ‘crimes’,” wrote Pappé, “was insisting that there was a massacre in the village of Tantura in 1948 as was exposed by MA student, Teddy Katz.”
Now, some Alexandroni Brigade veterans have finally confessed to the crimes in Tantura.
“They silenced it. It mustn’t be told, it could cause a whole scandal. I don’t want to talk about it, but it happened.” These were the words of Moshe Diamant, a former member of the Alexandroni Brigade who, with other veterans, revealed in the documentary “Tantura” by Alon Schwarz, the gory details of the horrific crimes that were committed in the Palestinian village.
An officer “killed one Arab after another” with his pistol, said former soldier Micha Vitkon. “They put them into a barrel and shot them in the barrel. I remember the blood in the barrel,” explained another. “I was a murderer. I didn’t take prisoners,” admitted Amitzur Cohen.
Hundreds of Palestinians were killed in Tantura in cold blood. They were buried in mass graves, the largest of which is believed to be under a car park at the Dor Beach, to which Israeli families flock daily.
The Tantura massacre is arguably the most glaring representation of “hidden” Israeli criminality on the occupation state’s roll call of shame. However, this is not the story of Tantura alone. The massacre in the village is representative of something much bigger, of ethnic cleansing on a huge scale, forceful evictions and mass killings. Thankfully, the truth is now being unearthed and exposed.
In another example, the Israeli army launched a full-scale military operation in 1951 to ethnically cleanse Palestinian Bedouins from the Naqab Desert. The tragic scenes of entire communities being uprooted from their ancestral homes were justified by Israel with the usual cliché that the terrible deed was carried out for “security reasons”.
In 1953, Israel passed the so-called Land Acquisition Law, which allowed the occupation state to seize the land of the Palestinians who had been forced out of their homes. By then, Israel had unlawfully expropriated 247,000 dunams of land in the Naqab, with 66,000 remaining “unutilised”. The remaining land is currently the epicentre of an ongoing saga involving Palestinian Bedouin communities in Israel and the Israeli government, which makes ludicrous claims that the land is “essential” for Israel’s “development needs”.
Extensive research conducted by Professor Gadi Algazi points to Israel’s narrative in the Naqab being a complete fabrication. According to numerous newly-revealed documents, Moshe Dayan, then the head of the Israeli army’s Southern Command, was central to an Israeli government and military ploy to evict the Bedouin population and to “revoke their rights as landowners”, under the conveniently created Israeli law, which allowed the government to “lease” the land as if it was its own.
“There was an organised transfer of Bedouin citizens from the north-western Negev eastward to barren areas, with the goal of taking over their lands,” Algazi told Haaretz. “They carried out this operation using a mix of threats, violence, bribery and fraud.”
The entire scheme was organised in such a way as to facilitate the claim that the Palestinians had moved “voluntarily”, despite their legendary resistance and “the stubbornness with which they tried to hold onto their land, even at the cost of hunger and thirst, not to mention the army’s threats and violence.”
Furthermore, a newly-released volume by French historian Vincent Lemire has entirely dismissed the official Israeli version of how the Moroccan Quarter in Jerusalem was demolished in June 1967. Although Palestinian and Arab historians have long argued that the destruction of the neighbourhood — 135 homes, two mosques and more — was done as per the order of the Israeli government through the then Jewish Mayor of Jerusalem, Teddy Kollek, Israel has just as long denied that version. According to the official Israeli account, the demolition of the neighbourhood was carried out by “15 private Jewish contractors [who] destroyed the neighbourhood to make space for the Western Wall plaza.”
In an interview with Agence France-Presse (AFP), Lemire said that his book offers “definitive, written proof on the pre-meditation, planning and coordination of this operation,” and that includes official meetings between Kollek, the commander of the Israeli army and other top government officials.
The story continues with more heartbreaking revelations as a well-integrated version of the truth exposing long-hidden or denied facts. The days of Israel getting away with these crimes seem to be behind us. For the third time in a little over twelve months, a major human rights organisation, on this occasion Amnesty International, has condemned Israeli apartheid.
Amnesty’s report, “Israel’s Apartheid against Palestinians: A Look into Decades of Oppression and Domination”, is 280 pages of damning evidence of Israel’s racism and apartheid. It does not shy away from connecting Israel’s violent present with its equally bloody past, nor does it borrow from Israel’s deceptive language and self-serving division of Palestinians into disconnected communities, each with a different claim and a different status. For Amnesty, as was the case with Human Rights Watch’s report in April last year, Israeli injustices against the Palestinians must be recognised and duly condemned in their entirety.
“Since its establishment in 1948, Israel has pursued an explicit policy of establishing and maintaining a Jewish demographic hegemony,” wrote Amnesty, “while minimising the number of Palestinians and restricting their rights.” This could only happen through mass killing, ethnic cleansing and genocide, from Tantura to the Naqab, to the Moroccan Quarter, the Gaza Strip and Sheikh Jarrah. The Israeli roll call of shame is long.
February 8, 2022
Posted by aletho |
Ethnic Cleansing, Racism, Zionism, Timeless or most popular, War Crimes | Human rights, Israel, Palestine, Zionism |
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Endless COVID-19 booster shots are being presented as the solution to the pandemic, as repeated injections increase the level of antibodies in your body.1 In December 2021, for instance, Moderna reported that their COVID-19 booster shot increased the level of antibodies by 37-fold, and when a full dose was given — the same amount used for the initial shots — antibody levels rose 83-fold.2
Pfizer and BioNTech have also announced that their booster shots increase antibody levels, but to what end? Artificially inflated antibodies signal to your body that you’re always infected, and the resulting immune response could prove to be detrimental to your health.
Such a condition can only lead to a “death zone,” accelerating the development of autoimmune conditions such as Parkinson’s, Kawasaki disease and multiple sclerosis, according to tech leader and COVID analyst Marc Girardot, who urges a retreat from the vaccination “death zone” before it’s too late.3
Are Boosters Taking Humans to the Death Zone?
Mountaineers are familiar with the “death zone,” which describes the top portion of the world’s tallest mountains — areas of such high altitude that oxygen is scarce, where humans can only survive for a matter of hours. “The same principle applies to our immune system,” Girardot explains, referring to the intense response our bodies mount in response to infection.
The response includes a high fever to damage virions, T-cell elevations and increased antibody production to rid your body of “viral debris.” This is designed to be a temporary response; after the threat is neutralized, your body tamps down its immune response. Girardot states:4
“Once the infection is gone, a regiment of sentinels is left in the mucus to guard the entrance for the remainder of the epidemic, a few roaming sentinels with lifelong memory are set, and the rest wanes back down to bring peace and balance. It’s called homeostasis. The fever dissipates. T-cells self-destruct rapidly. And antibodies wane progressively.”
This is by design, as a perpetual fever and high levels of antibodies keep your body in a dangerous state. Just as chronic stress — keeping your body in an extended state of “fight or flight mode” — increases disease risks, so, too, do permanently elevated levels of antibodies. Girardot details three reasons why:5
“1. Too long a fever would end up breaking down all healthy cells, and so the remedy would be worse than the illness.
2. Perpetual specialized T-cells are also dangerous as they can start off-target attacks of healthy cells (as often occurs with immune checkpoint blockade treatments against cancer), and would be like leaving your home filled with a battalion of armed soldiers with their guns loaded and pin-less hand-grenades.
3. Finally, very high levels of antibodies with nowhere to go are also extremely dangerous. They can passively bind to receptors of healthy cells, and kickstart a cascade of autoimmune diseases. Land mining where you live.”
Decreased Antibodies Isn’t a Measure of Waning Immunity
Remember, your immune system is designed to work in response to exposure to an infectious agent. Your adaptive immune system, specifically, generates antibodies that are used to fight pathogens that your body has previously encountered.6 During normal infections, high fever and temporary T-cell elevations, along with elevated antibodies to the infection, gradually dissipate.
However, declining antibodies shouldn’t be confused with declining immunity. Early data on SARS-CoV-2 also found that antibody titers declined rapidly in the first months after recovery from COVID-19, leading some to speculate — incorrectly — that protective immunity against SARS-CoV-2 may also be short-lived.7
Senior author of the study, Ali Ellebedy, Ph.D., an associate professor of pathology & immunology at Washington University School of Medicine in St. Louis, explained, “It’s normal for antibody levels to go down after acute infection, but they don’t go down to zero; they plateau.”8
A biphasic pattern of antibody concentrations against SARS-CoV-2 was uncovered,9 in which high antibody concentrations were found in the acute immune response that occurred at the time of initial infection. The antibodies declined in the first months after infection, as should be expected, then leveled off to about 10% to 20% of the maximum concentration detected.
When a new infection occurs, cells called plasmablasts provide antibodies, but when the virus is cleared, longer lasting memory B cells move in to monitor blood for signs of reinfection.10 Bone marrow plasma cells (BMPCs) also exist in bones, acting as “persistent and essential sources of protective antibodies.”11
According to Ellebedy, “A plasma cell is our life history, in terms of the pathogens we’ve been exposed to,”12 and it’s in these long-lived BMPCs were immunity to SARS-CoV-2 resides.
Among people who have recovered from COVID-19, most of the participants had BMPCs that secreted antibodies specific for the spike protein encoded by SARS-CoV-2 at both seven months and 11 months after infection.13 This is evidence of long-lasting immunity,14 even if levels of anti-SARS-CoV-2 spike protein (S) antibodies decline rapidly in the first four months after infection.
There’s a Cost to Massive, Artificially Elevated Antibodies
COVID-19 shots are poised for a perpetual cycle of ongoing booster shots every few months. After up to two doses of the initial shot, and a third booster already on the roster, a fourth booster is already being discussed, including by Moderna CEO Stéphane Bancel, who said that the efficacy of the third shot is likely to decline over several months, necessitating another shot soon thereafter.15
“Many politicians and vaccine manufacturers adamantly propose repeated injections, boosters every 3 or 4 months, as if waning antibodies were a sign of lost immunity,” Girardot said. “In reality, they are scapegoating the natural drop in antibodies. It is a smokescreen to hide their failure and the ineffectiveness of these intramuscular vaccines.”16
The reality is, repeatedly, artificially inflating antibodies comes with a cost. It’s known, for instance, that certain autoimmune diseases are seen alongside high levels of antibodies.17 Vaccine-induced autoimmunity is a well-known phenomenon, and molecular mimicry may be to blame.18
It occurs when similarities between different antigens confuse the immune system.19 There are often significant similarities between elements in the vaccine and human proteins, which can lead to immune cross-reactivity. When this occurs, researchers explained in Cellular & Molecular Immunology, “the reaction of the immune system towards the pathogenic antigens may harm the similar human proteins, essentially causing autoimmune disease.”20
In relation to COVID-19 shots, specifically, researchers wrote in the Journal of Autoimmunity, “Indeed, antibodies against the spike protein S1 of SARS-CoV-2 had a high affinity against some human tissue proteins. As vaccine mRNA codes the same viral protein, they can trigger autoimmune diseases in predisposed patients.”21
Already, case reports suggest that COVID-19 shots may trigger vaccine-induced immune-mediated and autoimmune hepatitis,22 and Girardot is concerned that repeated booster shots will only worsen outcomes:23
“In the case of an infection, the risk is relatively limited as the bulk of antibodies ends up binding to viral material circulating in large numbers. However, in the case of repeated doses, it’s very different.
After the second shot, it is likely that limited amounts of spike are produced as T-cells rapidly destroy production capacity. Thus, for most of us, large quantities of antibodies will inevitably be left idle circulating aimlessly, expanding exponentially (time x quantity) the risk of an accidental binding with catastrophic consequences.”
Natural Infection Produces Broad Immunity
Training your body to produce singular antibodies for one spike protein cannot compare to the protection provided by natural immunity, which occurs after recovery from an illness. Speaking with Daniel Horowitz, pathologist Dr. Ryan Cole explained that natural infection produces broad immunity that can’t be matched by vaccination:24
“A natural infection induces hundreds upon hundreds of antibodies against all proteins of the virus, including the envelope, the membrane, the nucleocapsid, and the spike. Dozens upon dozens of these antibodies neutralize the virus when encountered again.
Additionally, because of the immune system exposure to these numerous proteins (epitomes), our T cells mount a robust memory, as well. Our T cells are the ‘marines’ of the immune system and the first line of defense against pathogens. T cell memory to those infected with SARSCOV1 is at 17 years and running still.”
This may explain why a retrospective observational study published August 25, 2021, found that natural immunity is superior to immunity from COVID-19 shots, with researchers stating, “This study demonstrated that natural immunity confers longer lasting and stronger protection against infection, symptomatic disease and hospitalization caused by the Delta variant of SARS-CoV-2, compared to the BNT162b2 two-dose vaccine-induced immunity.”25
Pharmaceutical companies and health officials are making plans for ongoing boosters, including combination shots that include, for example, a COVID-19 shot, a flu shot and a respiratory syncytial virus (RSV) shot, in one injection — coming in 2023 — to avoid “compliance issues.”26
Nearly two dozen pathogens are currently being targeted for the development of new shots,27,28 and it’s likely that you’re going to see a continued push for more jabs and boosters. Will humans’ immune systems, and overall health, be able to withstand such an assault? Girardot doesn’t think so:29
“Today, I would like to underscore the absolute lunacy of delivering these products to an entire population every 3-4 months. It’s nothing short of criminal. In my earnest opinion, repeated vaccine injections can only lead to one outcome: generalized illness and death …
The vaccination ‘Death Zone’ exists, and we need to urgently go back down in the valley, we need to stop vaccinating, stop boosting aimless antibodies and trust our immune systems.”
Sources and References
February 8, 2022
Posted by aletho |
Science and Pseudo-Science, Timeless or most popular, War Crimes | Covid-19, COVID-19 Vaccine |
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An investigation into eight attacks attributed to the loyalist Ulster Defence Association (UDA) or the Ulster Freedom Fighters (UFF) has identified “significant failures” by UK authorities during the period known as The Troubles in Northern Ireland in the 1990s.
Laying out the findings in the 344-page report, published on Tuesday, Marie Anderson, the police ombudsman for Northern Ireland, claimed she was “deeply concerned” by the findings, which showed members of the police force, the Royal Ulster Constabulary (RUC), had deliberately destroyed files.
The “damning” investigation, which found “undiluted evidence of the policy of collusion,” stated that “11 murdered citizens and their families were systemically failed by the British state in life and in death.”
A spike in violence from loyalist paramilitary groups during the Troubles saw the RUC seek to expand its network of informants within the UDA and UFF. The RUC was condemned for a “totally unacceptable” practice of using informants who “were actively participating in serious criminality” and, in some cases, murders. However, the report did not find evidence that police had been handed information that could have stopped the attacks.
The Troubles, which lasted from the 1960s to the late 1990s, saw violent attacks and reprisals between Irish republican paramilitaries and Ulster loyalist groups. The UDA, which had tens of thousands of members at one point, has been deemed responsible for killing hundreds of people during the conflict. It was formally banned in August 1992, and announced in 2007 that “the war is over.” However, in 2018, then-Police Service of Northern Ireland Chief Constable George Hamilton claimed members of the UDA were still involved in criminal activities.
“Areas of the report make uncomfortable reading and I want to offer my sincere apologies to the families of those killed and injured for the failings identified in this report,” PSNI Temporary Assistant Chief Constable Jonathan Roberts said in a statement.
In his remarks, Roberts acknowledged the “continuing distress being felt by all of the families of those killed and injured in these attacks, and want to acknowledge the pain and suffering that they all continue to feel.”
February 8, 2022
Posted by aletho |
Civil Liberties, Deception, Timeless or most popular, War Crimes | Human rights, UK |
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The U.S. national-security establishment and its acolytes in the mainstream press are celebrating the U.S. military’s murder in Syria of Islamic State leader Abu Ibrahim Hashimi Qurayshi. Mind you, they don’t call it murder. They call it a “targeted killing” of a “bad guy” or a “terrorist.” But murder it is because the U.S. military has no legitimate authority to kill anyone in the Middle East (or anywhere else), whether it be people it labels “bad guys,” “terrorists,” “communists,” “opponents,” “rivals,” “adversaries,” or “enemies.”
Let’s take a look at the Bill of Rights, specifically the Fifth Amendment. Yes, I know that the national-security establishment and its supporters in the federal judiciary hold that the Bill of Rights doesn’t apply to the military, the CIA, and the NSA. But a close reading of the amendment reveals that there is no exception carved out for the national-security branch of the government. By its express terms, the restrictions in the Fifth Amendment apply to everyone in the federal government, not just to some people within the federal government.
The Fifth Amendment states in part: “No person shall be deprived of life without due process of law.”
Notice something important about that language: It doesn’t say “No American shall be deprived of life without due process of law.” It says “No person shall be deprived of life without due process of law.” That means it encompasses citizens of other countries.
Notice something else important: It doesn’t say “No person within the United States shall be deprived of life without due process of law.” It says “No person shall be deprived of life without due process of law.”
That’s what the Pentagon just did to Qurayshi. In a raid on a safe house in Syria, the Pentagon just deprived him of life without due process of law.
The Pentagon is pointing out that Qurayshi actually killed himself and his family with a bomb once the raid commenced. That doesn’t mean, of course, that the Pentagon isn’t responsible for killing him. The raid is the proximate cause of Qurayshi’s death as well as the deaths of other people who were with him, including women and children. That is, if the raid had not taken place, Qurayshi and those other people would still be alive.
In fact, the Pentagon is also responsible for the deaths of the women and children that were killed by Qurayshi’s suicide bomb. The Pentagon was well aware of the possibility that he could decide to blow himself up rather than be taken captive and carted away to Gitmo for torture and perpetual incarceration. That awareness did not stop them from conducting the raid anyway. The deaths of those women and children was a risk that the Pentagon felt was worth taking.
What is due process of law? It means notice and a trial. The Bill of Rights expressly prohibits the federal government from killing anyone without first giving him notice of criminal charges and a trial in federal district court. The notice comes in the form of a criminal indictment issued by a federal grand jury. At the trial, federal prosecutors are required to prove to a jury (or a judge) beyond a reasonable doubt that the accused is guilty of the offense for which they wish to kill him.
At the risk of belaboring the obvious, the Pentagon did not provide notice and a trial to Qurayshi before they raided that safe house and brought about his death and the deaths of more than a dozen other people. Perhaps the reason for that is that U.S. officials felt that they couldn’t prove that Qurayshi had committed a criminal offense against the United States.
National-security officials and their supporters implicitly claim that their “war on terrorism” trumps the Fifth Amendment. Really? Where does it say that in the Fifth Amendment? I certainly don’t see a “war on terrorism” exception in that amendment.
Indeed, what business do the Pentagon and the CIA have sitting in Syria and killing people? The last time I checked, Congress had not declared war on Syria. Moreover, the Syrian government has never invited the U.S. government to situate its troops and agents within the country. That makes the Pentagon and the CIA illegal interlopers in a foreign land, where they are killing whoever they want with impunity.
We also mustn’t forget that it is the Pentagon and the CIA that are responsible for the rise of ISIS in the first place, owing to their illegal and unconstitutional war of aggression against Iraq.
What is a “war of aggression”? It is a type of war that was declared a war crime at the Nuremberg War Crimes Tribunal. That was the tribunal that put accused Nazi war criminals on trial. The tribunal, which included U.S. officials, convicted German officials of attacking other nations. That’s what they called waging a “war of aggression.”
That’s what U.S. officials did with Iraq. It is undisputed that Iraq never attacked the United States. When the U.S. government attacked this impoverished third-world country, it was waging a “war on aggression.” Moreover, the fact that the Pentagon and the CIA did not secure the constitutionally required congressional declaration of war before committing this Nuremberg-type crime only makes the situation more egregious.
After U.S. officials installed a puppet regime with their war of aggression on Iraq, ISIS formed with the aim of ousting that U.S.-installed puppet regime. In fact, many of the ISIS members had been officials in the Saddam Hussein regime that was violently ousted from power by the U.S. invasion and occupation of the country. (It’s worth noting that Saddam was a partner and ally of the Pentagon and the CIA during the 1980s, when he was killing Iranians in his own war of aggression against Iran.)
Thus, if the U.S. government had never waged an illegal and unconstitutional war of aggression against Iraq, there never would have been an ISIS, which means that the man they just murdered — Abu Ibrahim Hashimi Qurayshi — would not have been the leader of ISIS, which means that he and his family would not be dead today.
Of course, Qurayshi will quickly be replaced, just like drug lords are quickly replaced after they are killed or captured by drug-war agents. ISIS will retaliate for Qurayshi’s killing, and the “war on terrorism” will continue, just as the drug war continues, which means ever-increasing budgets, power, and influence for the national-security establishment. The “war on terrorism” is a better racket than the “war on drugs” and perhaps even better than the old Cold War racket of the “war on communism.”
February 7, 2022
Posted by aletho |
Illegal Occupation, Timeless or most popular, War Crimes | CIA, Iraq, Syria, United States |
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THOUGH I ask this question as a layman, it hardly seems an unreasonable one. It is this:
What exactly is causing the increased risk of infection following vaccination, evidence of which was reported in the Daily Sceptic last week?
From the most recently published UKHSA Vaccine Surveillance Report data for those who are triple-jabbed and from other NHS data published on the double jabbed, the Daily Sceptic have been able to establish the infection rates by vaccination status as well as the unadjusted vaccine effectiveness for infection for those having two or three doses. The conclusion they reached is that the infection rates continue to be considerably worse in the vaccinated, both double and triple jabbed, which translates into what they describe as ‘highly negative unadjusted vaccine effectiveness estimates’. (My italics)
Their report emphasises that these figures are of rates per 100,000 and therefore already take into account the different sizes of the cohorts, meaning that their finding is not because there are more vaccinated people than unvaccinated in the population, and that factor is taken fully into account. You can read the full analysis here.
It is not just this report – which confirms the daily anecdotal evidence I am in receipt of about people I know to be double or triple vaccinated going down with Covid, especially since the booster was rolled out so determinedly – there also are the reports of surging cases in some of the most vaccinated of countries, most notably Israel. Much as Jacob Rees-Mogg and the Guardian, amongst others, really want to believe that it is unvaccinated who are commandeering all the available ventilators, this is not the case as Will Jones has previously laid bare.
On Saturday Dr Jones reported on the recent dramatic statement of one Professor Yaakov Jerris, the director of a coronavirus ward in an Israeli hospital, who has said that between 70 and 80 per cent of the serious cases in his hospital are fully vaccinated and how the vaccine has ‘no significance regarding severe illness’.
All of which brings me to the question of a phenomenon called Antibody Dependent Enhancement which I first heard of when Mike Yeadon warned about it last April under questioning from James Delingpole.
The term refers to the possibility that the vaccine-induced antibodies in the body somehow augment (rather than mitigate against) the infection when you actually catch it, or if these original antibodies don’t make the infection worse, subsequent booster jabs may well.
Could this be the reason for the spate of covid infection and illness? Could it even be the reason for the shocking surge in post-vaccine illnesses that Neville Hodgkinson reported here last week.
If so, was this a risk that the gene therapy vaccine researchers and producers were aware of?
All of which makes the battle over the FDA’s release of all documents related to the licensing of Pfizer’s Comirnaty COVID vaccine of all the more moment and importance. Their desire to keep their files secret for 75 years raises the question of what it is that they do not want us to know.
February 7, 2022
Posted by aletho |
Deception, Timeless or most popular, War Crimes | COVID-19 Vaccine |
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More evidence is surfacing showing that hospitals today are still collecting federal funds as an incentive to diagnose patients with “COVID” via a PCR Test, even if the patient was brought to the hospital with gunshot wounds, or to have a child, or from a car accident.
Project Veritas released a video yesterday of a whistleblower, Jeanne Stagg, who was working as a Senior Administrative Nurse at United Healthcare in Louisiana.
She came forward to expose the fraudulent practices still going on in hospitals today where people who have no symptoms of COVID come into the hospital, such as from gunshot wounds, or to have a baby, or because they were in a car accident, and are then tested positive for COVID and coded as a “COVID patient” when they are admitted to the hospital.
This releases federal funding that financially benefits the hospitals, but can literally kill the patient because they get the wrong treatment.
And to demonstrate how this is happening, a man has just come forward to give his testimony in public about how he was in a car accident, where EMS ambulance services arrived on the scene and sedated him against his will, air lifted him to a hospital allegedly in Tucson, Arizona, and he woke up 8 hours later on a ventilator because he was diagnosed as a “COVID” patient.
He was all alone in his room when he woke up, so he took himself off of the ventilator, removed the IV and catheter, and demanded to be released from the hospital.
He considers himself lucky to be alive today.
This is on our Bitchute channel, and also on our Telegram channel.
February 5, 2022
Posted by aletho |
Corruption, Deception, Timeless or most popular, Video, War Crimes | Covid-19, United States |
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New Zealand – The Medsafe report Adverse events following immunisation with COVID-19 vaccines: Safety Report #39 – 31 December 2021 lists 46,000 adverse events reported since the start of the Pfizer vaccine rollout in New Zealand. Historically this is 30 times the rate of adverse effects reported for flu vaccines. More than 50 per cent of these adverse effects are reported by medical professionals and about 40 per cent by affected members of the public via the CARM (Centre for Adverse Reactions Monitoring) website. Prior experience published by Medsafe concludes that only 5 per cent of adverse events are reported to CARM. A total of 8.1million doses have been administered in NZ.
The ten most common adverse events
Some 44,000 of the 46,000 adverse events are dismissed by Medsafe as ‘non-serious’—a number which has been echoed by politicians across the NZ political spectrum and by our Ministry of Health as evidence that the Pfizer vaccine is safe. The ten most common adverse events (all rated as non-serious) are as follows (from Medsafe). The total number of events below is more than 44,000 because many people experienced multiple symptoms.
The Mayo Clinic in USA reported before the pandemic that the risk of developing myocarditis is rare and lists the following concerning symptoms of myocarditis:
Mayo Clinic—Myocarditis Symptoms
If you’re in the early stages of myocarditis, you might have mild symptoms such as chest pain, rapid or irregular heartbeats, or shortness of breath. Some people with early-stage myocarditis don’t have any symptoms. The signs and symptoms of myocarditis vary, depending on the cause of the disease. Common myocarditis signs and symptoms include:
• Chest pain
• Rapid or irregular heartbeat (arrhythmias)
• Shortness of breath, at rest or during activity
• Fluid buildup with swelling of the legs, ankles and feet
• Fatigue
• Other signs and symptoms of a viral infection such as a headache, body aches, joint pain, fever, child dizziness, a sore throat or diarrhea
Sometimes, myocarditis symptoms may be similar to a heart attack. If you are having unexplained chest pain and shortness of breath, seek emergency medical help.
Of the ten most common adverse effects of Covid-19 vaccination reported to CARM in NZ, you can see eight are listed as symptoms of myocarditis by the Mayo Clinic. Given that myocarditis is the most common known severe outcome of Covid-19, why have the eight common vaccine adverse effects also known to be symptoms of myocarditis been characterised as ‘non-serious’? Is this a glaring case of misdiagnosis? If so, why?
NZ GPs and medical personnel had a naive expectation of vaccine safety
The first point to note is that most NZ medical professionals had expectations of vaccine safety based both on years of experience with vaccination programmes and the extensive medical education they had received. They had no prior experience with drugs or vaccines which had not already completed years of testing and safety evaluation. It was for them therefore virtually unthinkablethat the Pfizer vaccine was unsafe. Moreover the Pfizer vaccine trial results had already characterised the common adverse effects as non-serious. For this reason the very common reports of chest discomfort and shortness of breathfollowing Covid-19 vaccination, which according to prior protocols should have led to intensive investigation and treatment, were dismissed as non-serious without investigation and in most cases without reporting to CARM. Perhaps their very common occurrence fostered an attitude of indifference and dismissal which many victims suffered in NZ when they reported such symptoms to their GP or to hospital staff.
Rates of Myocarditis symptoms are higher than realised
The prevalence of a wide range of known myocarditis symptoms is probably indicative of a very high rate of subclinical and mild myocarditis following Pfizer vaccination. The important point to note is that the recommended treatment for mild myocarditis is rest. Most people recover if it is treated early with sufficient prolonged rest. If left untreated, myocarditis can restrict the capacity of the heart to pump blood which can lead to serious cardiac events such as heart attack, stroke, and arrhythmia. It is wrong to undertake vigorous physical activity including sport while suffering from myocarditis. It is clear from this that insufficient precautionary instructions were given to vaccine recipients about the risks they faced and the steps that they needed to take to avoid these risks. This may have contributed to cardiac problems including among some recipients undertaking vigorous physical exercise.
The possible extent of these cardiac events is indicated by multiple reports to voluntary organisations. An important point to note here is that reporting to CARM is not mandatory, a very unfortunate yet unforgivably deliberate omission. Medsafe attempts in its Safety Report #39 (referenced above) to dismiss the significance of adverse events by comparing their rate to population norms. In the absence of mandatory reporting, especially considering that Medsafe knows adverse events are grossly under-reported, all such comparisons are statistically meaningless.
A public information campaign is essential
Belatedly Dr Ashley Bloomfield, Director General of the Ministry of the Health, struck a note of alarm about myocarditis in his December 15 2021 letter to directors of district health boards, but this concern did not alter much the processes being applied. Individuals experiencing myocarditis following their first vaccination are still being denied exemptions. Those suffering strokes and heart attacks are in some if not most cases being denied Accident Compensation Commission (ACC) assistance. There is also a virtual data black-out on rates of cardiac events and hospitalisations and on ACC claims. Anecdotal and whistleblower reports here and overseas suggest these might be high but considering that data collection has been haphazard due to the ‘non-serious’ label, these might be hard to quantify unless the government makes an honest attempt to inform the public of risks and ask people to come forward who are already affected. This is particularly important as many stroke, cardiac and other serious adverse event sufferers have already been emphatically informed by their GP or other medical professionals that their symptoms must be unrelated to the Pfizer vaccination – an egregious form of victim-blaming lacking any scientific basis.
For more information: HatchardReport.com
February 4, 2022
Posted by aletho |
Science and Pseudo-Science, War Crimes | COVID-19 Vaccine, New Zealand |
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The European (EEA and non-EEA countries) database of suspected drug reaction reports is EudraVigilance, verified by the European Medicines Agency (EMA), and they are now reporting 38,983 fatalities, and 3,530,362 injuries following injections of four experimental COVID-19 shots:
From the total of injuries recorded, almost half of them (1,672,872 ) are serious injuries.
“Seriousness provides information on the suspected undesirable effect; it can be classified as ‘serious’ if it corresponds to a medical occurrence that results in death, is life-threatening, requires inpatient hospitalisation, results in another medically important condition, or prolongation of existing hospitalisation, results in persistent or significant disability or incapacity, or is a congenital anomaly/birth defect.”
A Health Impact News subscriber in Europe ran the reports for each of the four COVID-19 shots we are including here. It is a lot of work to tabulate each reaction with injuries and fatalities, since there is no place on the EudraVigilance system we have found that tabulates all the results.
Since we have started publishing this, others from Europe have also calculated the numbers and confirmed the totals.*
Here is the summary data through January 29, 2022.
Total reactions for the mRNA vaccine Tozinameran (code BNT162b2,Comirnaty) from BioNTech/ Pfizer: 17,578 deaths and 1,704,757 injuries to 29/01/2022
- 48,240 Blood and lymphatic system disorders incl. 242 deaths
- 57,541 Cardiac disorders incl. 2,554 deaths
- 522 Congenital, familial and genetic disorders incl. 51 deaths
- 22,590 Ear and labyrinth disorders incl. 11 deaths
- 1,911 Endocrine disorders incl. 6 deaths
- 25,814 Eye disorders incl. 38 deaths
- 133,365 Gastrointestinal disorders incl. 681 deaths
- 422,360 General disorders and administration site conditions incl. 5,024 deaths
- 1,931 Hepatobiliary disorders incl. 90 deaths
- 18,455 Immune system disorders incl. 95 deaths
- 76,443 Infections and infestations incl. 1,878 deaths
- 33,972 Injury, poisoning and procedural complications incl. 331 deaths
- 42,585 Investigations incl. 502 deaths
- 11,344 Metabolism and nutrition disorders incl. 273 deaths
- 201,643 Musculoskeletal and connective tissue disorders incl. 212 deaths
- 1,629 Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 153 deaths
- 278,744 Nervous system disorders incl. 1,859 deaths
- 2,513 Pregnancy, puerperium and perinatal conditions incl. 74 deaths
- 251 Product issues incl. 3 deaths
- 30,622 Psychiatric disorders incl. 207 deaths
- 6,150 Renal and urinary disorders incl. 266 deaths
- 68,129 Reproductive system and breast disorders incl. 6 deaths
- 72,531 Respiratory, thoracic and mediastinal disorders incl. 1,884 deaths
- 78,059 Skin and subcutaneous tissue disorders incl. 146 deaths
- 3,871 Social circumstances incl. 22 deaths
- 21,010 Surgical and medical procedures incl. 204 deaths
- 42,532 Vascular disorders incl. 766 deaths
Total reactions for the mRNA vaccine mRNA-1273 (CX-024414) from Moderna: 11,008 deaths and 543,543 injuries to 29/01/2022
- 12,365 Blood and lymphatic system disorders incl. 120 deaths
- 18,287 Cardiac disorders incl. 1,142 deaths
- 190 Congenital, familial and genetic disorders incl. 11 deaths
- 6,310 Ear and labyrinth disorders incl. 8 deaths
- 502 Endocrine disorders incl. 6 deaths
- 7,475 Eye disorders incl. 36 deaths
- 44,340 Gastrointestinal disorders incl. 413 deaths
- 145,153 General disorders and administration site conditions incl. 3,630 deaths
- 793 Hepatobiliary disorders incl. 54 deaths
- 5,370 Immune system disorders incl. 22 deaths
- 23,070 Infections and infestations incl. 1042 deaths
- 10,286 Injury, poisoning and procedural complications incl. 208 deaths
- 12,129 Investigations incl. 393 deaths
- 4,847 Metabolism and nutrition disorders incl. 263 deaths
- 66,358 Musculoskeletal and connective tissue disorders incl. 223 deaths
- 682 Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 85 deaths
- 91,230 Nervous system disorders incl. 1,029 deaths
- 907 Pregnancy, puerperium and perinatal conditions incl. 10 deaths
- 98 Product issues incl. 4 deaths
- 9,441 Psychiatric disorders incl. 181 deaths
- 3,030 Renal and urinary disorders incl. 214 deaths
- 12,547 Reproductive system and breast disorders incl. 9 deaths
- 23,251 Respiratory, thoracic and mediastinal disorders incl. 1,162 deaths
- 27,540 Skin and subcutaneous tissue disorders incl. 96 deaths
- 2,239 Social circumstances incl. 45 deaths
- 3,028 Surgical and medical procedures incl. 203 deaths
- 12,075 Vascular disorders incl. 399 deaths
Total reactions for the vaccine AZD1222/VAXZEVRIA (CHADOX1 NCOV-19) from Oxford/ AstraZeneca: 7,977 deaths and 1,154,757 injuries to 29/01/2022
- 13,912 Blood and lymphatic system disorders incl. 278 deaths
- 20,984 Cardiac disorders incl. 830 deaths
- 235 Congenital familial and genetic disorders incl. 8 deaths
- 13,406 Ear and labyrinth disorders incl. 7 deaths
- 692 Endocrine disorders incl. 6 deaths
- 20,086 Eye disorders incl. 32 deaths
- 107,453 Gastrointestinal disorders incl. 434 deaths
- 304,993 General disorders and administration site conditions incl. 1,855 deaths
- 1,039 Hepatobiliary disorders incl. 69 deaths
- 5,409 Immune system disorders incl. 40 deaths
- 42,266 Infections and infestations incl. 620 deaths
- 13,630 Injury poisoning and procedural complications incl. 198 deaths
- 25,681 Investigations incl. 205 deaths
- 13,023 Metabolism and nutrition disorders incl. 126 deaths
- 168,174 Musculoskeletal and connective tissue disorders incl. 165 deaths
- 743 Neoplasms benign malignant and unspecified (incl cysts and polyps) incl. 40 deaths
- 234,117 Nervous system disorders incl. 1,178 deaths
- 635 Pregnancy puerperium and perinatal conditions incl. 20 deaths
- 199 Product issues incl. 1 death
- 21,051 Psychiatric disorders incl. 69 deaths
- 4,338 Renal and urinary disorders incl. 78 deaths
- 16,849 Reproductive system and breast disorders incl. 3 deaths
- 41,401 Respiratory thoracic and mediastinal disorders incl. 1,082 deaths
- 52,064 Skin and subcutaneous tissue disorders incl. 65 deaths
- 1,617 Social circumstances incl. 9 deaths
- 1,973 Surgical and medical procedures incl. 30 deaths
- 28,787 Vascular disorders incl. 529 deaths
Total reactions for the COVID-19 vaccine JANSSEN (AD26.COV2.S) from Johnson & Johnson: 2,420 deaths and 127,305 injuries to 29/01/2022
- 1,229 Blood and lymphatic system disorders incl. 51 deaths
- 2,552 Cardiac disorders incl. 204 deaths
- 40 Congenital, familial and genetic disorders incl. 1 death
- 1,319 Ear and labyrinth disorders incl. 3 deaths
- 105 Endocrine disorders incl. 1 death
- 1,656 Eye disorders incl. 10 deaths
- 9,588 Gastrointestinal disorders incl. 88 deaths
- 34,487 General disorders and administration site conditions incl. 685 deaths
- 153 Hepatobiliary disorders incl. 13 deaths
- 544 Immune system disorders incl. 10 deaths
- 8,521 Infections and infestations incl. 207 deaths
- 1,147 Injury, poisoning and procedural complications incl. 25 deaths
- 6,086 Investigations incl. 131 deaths
- 756 Metabolism and nutrition disorders incl. 60 deaths
- 17,116 Musculoskeletal and connective tissue disorders incl. 55 deaths
- 86 Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 8 deaths
- 23,413 Nervous system disorders incl. 245 deaths
- 55 Pregnancy, puerperium and perinatal conditions incl. 1 death
- 30 Product issues
- 1,766 Psychiatric disorders incl. 22 deaths
- 535 Renal and urinary disorders incl. 31 deaths
- 2,941 Reproductive system and breast disorders incl. 6 deaths
- 4,468 Respiratory, thoracic and mediastinal disorders incl. 304 deaths
- 3,760 Skin and subcutaneous tissue disorders incl. 10 deaths
- 409 Social circumstances incl. 4 deaths
- 867 Surgical and medical procedures incl. 74 deaths
- 3,676 Vascular disorders incl. 171 deaths

*These totals are estimates based on reports submitted to EudraVigilance. Totals may be much higher based on percentage of adverse reactions that are reported. Some of these reports may also be reported to the individual country’s adverse reaction databases, such as the U.S. VAERS database and the UK Yellow Card system. The fatalities are grouped by symptoms, and some fatalities may have resulted from multiple symptoms.
On January 29, 2021 a mass funeral protest for children who have died after receiving a Pfizer vaccine was held in Geneva, Switzerland.
Someone recorded the event and made a short video. This is on our Bitchute Channel, and also on our Telegram channel.
February 4, 2022
Posted by aletho |
Civil Liberties, Video, War Crimes | COVID-19 Vaccine, European Union, Human rights |
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The U.S. Food and Drug Administration (FDA) on Monday granted full approval of Moderna’s Spikevax COVID vaccine for people 18 and older.
Similar to the agency’s licensing last year of Pfizer’s Comirnaty vaccine, the approval raised a number of legal questions related to mandates and product availability.
Spikevax is a two-dose primary series, approved also for administration as part of a heterologous (“mix and match”) single booster dose for individuals who previously completed their original series of vaccinations with the Pfizer or Johnson & Johnson COVID vaccines.
According to the FDA, Spikevax “has the same formulation as the [Emergency Use Authorization (EUA)] Moderna COVID-19 Vaccine and … can be used interchangeably with the EUA Moderna COVID-19 Vaccine to provide the COVID-19 vaccination series.”
However, in its approval letter, the FDA said Spikevax is “legally distinct” from the Moderna EUA vaccine:
“The licensed vaccine has the same formulation as the EUA-authorized vaccine and the products can be used interchangeably to provide the vaccination series without presenting any safety or effectiveness concerns. The products are legally distinct with certain differences that do not impact safety or effectiveness.”
The FDA made the same distinction between the Pfizer-BioNTech EUA vaccine and the Pfizer Comirnaty vaccine, which the agency fully licensed in August, 2021, a move that raised questions about liability and the legality of vaccine mandates.
After Monday’s announcement, media outlets were quick to reassure the public the two Moderna vaccines are the same and that this was just a marketing ploy, where Moderna simply “rebranded” what is otherwise the same vaccine.
No ‘fully licensed’ COVID actually available
While Moderna’s Spikevax vaccine is now fully licensed, the original Moderna vaccine will remain under EUA. Indeed, the FDA on Jan. 7 reissued the EUA.
The FDA has also made it clear the Spikevax vaccine will not be available to the American public, announcing:
“Although SPIKEVAX (COVID-19 Vaccine, mRNA) and Comirnaty (COVID-19 Vaccine, mRNA) are approved to prevent COVID-19 in certain individuals within the scope of the Moderna COVID-19 Vaccine authorization, there is not sufficient approved vaccine available for distribution to this population in its entirety at the time of reissuance of this EUA.”
These claims parallel the chain of events that followed the FDA’s full approval of the Pfizer Comirnaty vaccine in August 2021.
At the time, Pfizer and the FDA claimed Comirnaty was not yet available, as there were sufficient stocks of the Pfizer-BioNTech EUA vaccine still available to be administered.
As of this writing, the FDA states, via its website, that Comirnaty products are “not orderable at this time.”
The FDA has not indicated when, or if, the Spikevax and Comirnaty vaccines will be available for distribution in the U.S.
Are EUA and fully licensed vaccines really interchangeable?
As reported by The Defender, there is a significant legal distinction between products authorized under EUA and those fully licensed by the FDA.
EUA products are experimental under U.S. law. Under the Nuremberg Code and federal regulations, no one can force a human being to participate in this experiment.
Specifically, under 21 U.S. Code Sec.360bbb-3(e)(1)(A)(ii)(III), “authorization for medical products for use in emergencies,” it is unlawful to deny someone a job or an education because they refuse to be an experimental subject. Instead, potential recipients have an absolute right to refuse EUA vaccines.
That’s an issue military members, unable to find any vaccination sites that offer the fully licensed Comirnaty vaccine, cited in various lawsuits challenging vaccine mandates.
Notably, on Nov. 12, 2021, a federal judge rejected an argument by the U.S. Department of Defense, in defending the military’s vaccine mandate, that the Pfizer Comirnaty and Pfizer-BioNTech vaccines are “interchangeable.”
U.S. law also requires the EUA designation be used only when “there is no adequate, approved and available alternative to the product for diagnosing, preventing or treating such disease or condition.”
This means that, in legal terms, all EUA products should be withdrawn once alternative products have received full approval.
Perhaps the most significant legal distinction, however, pertains to the legal protections afforded vaccine manufacturers, depending on how their product is classified.
Under the 2005 Public Readiness and Preparedness (PREP) Act, EUA-approved vaccines enjoy a significant liability shield. Specifically, vaccine manufacturers, distributors, providers, and government officials involved in the policymaking, approval, and distribution process are immune from any legal liability.
Under such regulations, the only way an injured party can sue is if he or she can prove willful misconduct, and if the U.S. government has also brought an enforcement action against the party for willful misconduct.
No such lawsuit has ever succeeded.
Conversely, fully licensed vaccines, such as Spikevax and Comirnaty, do not have a liability shield, and are instead subject to the same product liability laws as other products.
This means the Spikevax and Comirnaty vaccines could expose pharmaceutical companies to significant financial claims if individuals injured by the vaccines chose to sue the vaccine makers.
The rush to get COVID vaccines authorized for all ages — a ploy to avoid liability?
There’s another reason Pfizer and Moderna don’t want their fully licensed vaccines to be available yet — they’re waiting for the vaccines to be authorized, then licensed, for children as young as 6 months old.
Why? Because once a vaccine is fully licensed by the FDA, the only way its manufacturer can be shielded from legal liability is if the vaccine is added to the Centers for Disease Control and Prevention’s childhood vaccination schedule.
The National Childhood Vaccine Injury Act (NCVIA), passed into law in 1986, provides a legal liability shield to drugmakers if they receive full authorization for all ages and the vaccine is added to the mandatory schedule.
Reporting on the FDA’s approval of Spikevax, investigative journalist Jordan Schachtel wrote:
“Are Pfizer and Moderna waiting for full authorization for children’s shots to distribute Comirnaty and Spikevax to the masses? There’s plenty of litigators who have suggested that this is exactly what is going on in Big Pharma world.”
By creating the public perception that the Pfizer and Moderna EUA vaccines are fully approved, businesses, schools and other institutions are emboldened to impose vaccine mandates that violate existing law and allow the vaccines to be administered without informed consent.
It has also been argued that by relabeling the product, any previous data regarding vaccine injuries and side effects identified in association with the EUA vaccine are not counted in the safety studies for the approved vaccine.
The FDA approval of the Pfizer Comirnaty vaccine, its subsequent lack of availability and the continued administration of the Pfizer-BioNTech EUA vaccine led Children’s Health Defense (CHD) to file a lawsuit against the FDA and its acting director, Dr. Janet Woodcock, for their allegedly deceptive and rushed approval of the Comirnaty vaccine, arguing that the approval represented a classic “bait and switch” tactic.
CHD further alleged in its lawsuit that the FDA violated federal law when it simultaneously licensed Pfizer’s Comirnaty vaccine and extended Pfizer’s EUA — as the agency has now done with Moderna and Spikevax — for a vaccine that has the “same formulation” and that “can be used interchangeably,” according to the FDA.
FDA admits no safety data for Spikevax use among pregnant women
Beyond the legal questions raised by the FDA’s approval this week of Spikevax, the approval also raises safety questions.
For instance, the FDA admitted Spikevax was insufficiently tested on pregnant women, stating that “[a]vailable data on SPIKEVAX administered to pregnant women are insufficient to inform vaccine-associated risks in pregnancy.”
Furthermore, Spikevax was approved without having been tested for its ability to provide protection against the Omicron variant, which is reported to account for 99.9% of current U.S. COVID cases — it was approved only for providing protection against mutations that are no longer circulating.
And yet, the FDA cited the Omicron variant as the reason behind its decision to pull its EUA for monoclonal antibody products. The FDA claims that these products have not been shown to provide protection against the Omicron variant.
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.
February 3, 2022
Posted by aletho |
Deception, Timeless or most popular, War Crimes | COVID-19 Vaccine, FDA, Moderna, Pfizer, Spikevax, United States |
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The Costa Rica Ministry of Health in conjunction with the National Children’s Board (PANI) gave hospital officials the authorization to vaccinate all children in their care as long as there are no medical counter indications that would preclude it.
The issue arose after the parents of a child in a hospital in Heredia objected to their child being vaccinated after the child tested positive for Covid-19. Ultimately the child was vaccinated and discharged but only after a protest that became violent when a group organized online tried to remove the child from the hospital, resulting in the arrests of seven people.
In a statement from PANI they cited the the hosipital had the legal authority and the “fundamental right to health and life” of the child as paramount and part of the basis of the order.
While the first vaccination was administered it seems unlikely that the parents will follow up for any future Covid-19 vaccinations or that the Ministry of Health will intervene if the child is no longer under their care.
What is also unclear is if any other Costa Rica authorities will take any actions against the parents for failing to vaccinate their child in the future.
February 2, 2022
Posted by aletho |
Civil Liberties, War Crimes | Costa Rica, COVID-19 Vaccine, Human rights |
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