• 🚨 Study Claims COVID Caused More Heart Damage Than Vaccines — Here’s What the Authors Got Wrong

    Rainer Johannes Klement, Ph.D + Harald Walach reanalyzed data and found that while coronaviruses might cause myocarditis, the COVID-19 vaccines cause at least as much or more.

    Study Claims COVID Caused More Heart Damage Than Vaccines — Here’s What the Authors Got Wrong
    A 2023 study admitted that the COVID-19 mRNA vaccines cause myocarditis, but claimed the COVID-19 virus was even more damaging than the vaccine. A recent, more detailed review of their data, however, showed the opposite is likely true.

    Angelo DePalma, Ph.D.
    human heart with covid vaccine
    Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free.

    Despite the known side effects of mRNA COVID-19 vaccines, some studies (here, here and here) and health websites (here, here and here) argue that whatever vaccination’s adverse outcomes, being unvaccinated is worse.

    In one such study, Dr. Christian Mueller and his co-authors concluded the COVID-19 virus — not the vaccine — was responsible for more myocarditis, or heart muscle damage, than the vaccine.

    However, when Rainer Johannes Klement, Ph.D., a physicist at Leopoldina Hospital in Schweinfurt, Germany, and Harald Walach, a clinical psychologist and head of the Change Health Institute in Basel, Switzerland, reanalyzed Mueller’s data they found that while coronaviruses might cause myocarditis, the COVID-19 vaccines cause at least as much or more.

    The Klement paper appeared in the Feb. 1 edition of The Egyptian Health Journal.

    Mueller’s study

    Mueller set out to quantify and compare myocarditis in vaxed versus unvaxed subjects and to explain possible mechanisms.

    To explore these mechanisms, the researchers tested subjects for antibodies against interleukin-1 receptor antagonist (IL-1RA), the SARS-CoV-2-nucleoprotein, the viral spike protein and 14 inflammatory cytokines.

    Since none of these measures differed between study groups, the “mechanism” issue was unresolved.

    To assess myocarditis investigators tested 777 hospital workers (median age 37, 69.5% women) for cardiac troponin T one and three days after they received an mRNA-1273 booster. Cardiologists typically prescribe this test after a suspected heart attack to quantify the extent and duration of heart damage.

    Of the 40 subjects (5.1%) with elevated troponin on Day 3, 22 (2.8%) were diagnosed with myocarditis, with 20 cases occurring in women and two in men.

    The researchers reported that among these subjects troponin elevations were mild and temporary and did not involve abnormalities as determined by electrocardiogram. No patients experienced “major adverse cardiac events” within 30 days of receiving the shot.

    Mueller’s team concluded:

    COVID-19 associates with a substantially higher risk for myocarditis that [sic] mRNA vaccination …
    Myocarditis related to COVID-19 infection has shown a higher mortality than myocarditis related to mRNA vaccination.
    Before the COVID-19 vaccine were [sic] available, the incidence and extent of myocardial injury associated with COVID-19 infection was [sic] much higher than observed in this active surveillance study after booster vaccination.
    One of the Mueller co-authors had commercial ties to diagnostics companies. Another had previously been compensated by diagnostics and vaccine manufacturers. Mueller had relationships with diagnostics, pharmaceutical and vaccine companies at the time he wrote the paper.

    Where did Mueller go wrong?

    One way to measure treatment effects is to compare an outcome, for example, blood pressure, in the same subjects before and after the treatment and report before-and-after results.

    Although this option was known to medical researchers and available to him, Mueller did not take advantage of it — either because he did not think to measure pre-booster troponin levels or chose not to report them for some reason, perhaps because they did not align with his other results.

    Instead, his team took an approach that required two well-matched study groups. Although Mueller claimed placebos and controls met this requirement they differed on the feature that mattered most: heart health.

    Vaccinated subjects with current or recent heart issues were excluded from the study, while all control subjects had just entered the hospital with heart symptoms and were therefore already at greater risk for myocarditis.

    Klement and Walach found more anomalies in the Mueller paper.

    RFK Jr. and Brian Hooker Vax-Unvax
    RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax”

    Order Now

    They began their critique by citing three 2021 studies on COVID-19 vaccine-induced myocarditis (here, here and here). All three studies showed myocarditis became a concern shortly after the COVID-19 vaccine introductions.

    They discussed three papers in some detail:

    A 2023 German autopsy study on 25 unexpected deaths within 20 days of COVID-19 vaccination identified acute myocarditis as the most probable cause of death in four cases.
    A 2023 report on myocarditis in 303 non-vaccinated and 700 vaccinated asymptomatic subjects found significantly higher damage in the vaccinated persisting for up to 180 days post-vaccination.
    One of the first autopsy papers, an Indian-led study based on World Health Organization pharmacovigilance data reported 2.1 times the risk for cardiac arrest, 2.7 times the risk for acute heart attack, 2.6 times the risk for elevated troponin, and 7.3-fold higher levels of D-dimer for COVID-19 vaccinations compared with the use of other medications.
    These studies strongly suggest that myocarditis became an issue only after the mRNA vaccine rollouts. They contradict Mueller’s statement that the “extent of myocardial injury associated with COVID-19 infection was much higher than observed in this active surveillance study after booster vaccination.”

    According to Klement and Walach, this statement is wrong for two reasons.

    First, in addition to the non-equivalence of controls’ and subjects’ heart-health status, Mueller ignored the much larger number of COVID-19-infected, unhospitalized, unvaccinated individuals with (presumably) much lower troponin levels compared with patients entering the hospital with heart symptoms.

    Second, Klement and Walach argued that the public health impact of myocarditis depends not only on the incidence or rate among study groups but the size of those groups. The significance is that a lower incidence in a very large group (vaccinated) is more meaningful than a slightly higher rate in a very small group (individuals infected with COVID-19).

    scales of justice
    Your support helps fund this work, and CHD’s related advocacy, education and scientific research.

    Donate Now

    On that basis, Klement and Walach estimated the number of myocarditis cases among all German COVID-19 hospitalizations at 27,467, and among those who were vaccinated at 1.97 million.

    As a result, regardless of myocarditis severity, there were 71.7 times as many myocarditis cases among the vaccinated as among those hospitalized for COVID-19.

    A similar analysis for Switzerland estimated 169,960 cases of myocarditis among vaccinated compared with 8,179 among those hospitalized for COVID-19. Although not as dramatic as the German estimates this still shows a much higher occurrence of heart damage among vaccinated versus hospitalized.

    In a June 2021 paper, Walach, Klement and Dutch data analyst Wouter Aukema concluded that based on 700 adverse reactions, 16 serious side effects and 4.11 deaths for every 100,000 vaccinations, COVID-19 vaccines were released with insufficient safety data.

    The authors said the risk-benefit ratio for mRNA vaccines did not add up because “for three deaths prevented by vaccination we have to accept two inflicted by vaccination.”

    Mueller told The Defender via email:

    “Our study reveals an important lack of prospective safety data concerning COVID-19 vaccines. Given the magnitude of the vaccinated population compared to the much smaller proportion of the population that became infected and developed symptoms, including a small percentage with possible heart damage, our findings should remain qualitatively robust.”

    LEARN MORE ⬇️
    https://childrenshealthdefense.org/defender/covid-study-myocarditis-vaccines/

    Join ➡️ @ShankaraChetty
    🚨 Study Claims COVID Caused More Heart Damage Than Vaccines — Here’s What the Authors Got Wrong Rainer Johannes Klement, Ph.D + Harald Walach reanalyzed data and found that while coronaviruses might cause myocarditis, the COVID-19 vaccines cause at least as much or more. Study Claims COVID Caused More Heart Damage Than Vaccines — Here’s What the Authors Got Wrong A 2023 study admitted that the COVID-19 mRNA vaccines cause myocarditis, but claimed the COVID-19 virus was even more damaging than the vaccine. A recent, more detailed review of their data, however, showed the opposite is likely true. Angelo DePalma, Ph.D. human heart with covid vaccine Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. Despite the known side effects of mRNA COVID-19 vaccines, some studies (here, here and here) and health websites (here, here and here) argue that whatever vaccination’s adverse outcomes, being unvaccinated is worse. In one such study, Dr. Christian Mueller and his co-authors concluded the COVID-19 virus — not the vaccine — was responsible for more myocarditis, or heart muscle damage, than the vaccine. However, when Rainer Johannes Klement, Ph.D., a physicist at Leopoldina Hospital in Schweinfurt, Germany, and Harald Walach, a clinical psychologist and head of the Change Health Institute in Basel, Switzerland, reanalyzed Mueller’s data they found that while coronaviruses might cause myocarditis, the COVID-19 vaccines cause at least as much or more. The Klement paper appeared in the Feb. 1 edition of The Egyptian Health Journal. Mueller’s study Mueller set out to quantify and compare myocarditis in vaxed versus unvaxed subjects and to explain possible mechanisms. To explore these mechanisms, the researchers tested subjects for antibodies against interleukin-1 receptor antagonist (IL-1RA), the SARS-CoV-2-nucleoprotein, the viral spike protein and 14 inflammatory cytokines. Since none of these measures differed between study groups, the “mechanism” issue was unresolved. To assess myocarditis investigators tested 777 hospital workers (median age 37, 69.5% women) for cardiac troponin T one and three days after they received an mRNA-1273 booster. Cardiologists typically prescribe this test after a suspected heart attack to quantify the extent and duration of heart damage. Of the 40 subjects (5.1%) with elevated troponin on Day 3, 22 (2.8%) were diagnosed with myocarditis, with 20 cases occurring in women and two in men. The researchers reported that among these subjects troponin elevations were mild and temporary and did not involve abnormalities as determined by electrocardiogram. No patients experienced “major adverse cardiac events” within 30 days of receiving the shot. Mueller’s team concluded: COVID-19 associates with a substantially higher risk for myocarditis that [sic] mRNA vaccination … Myocarditis related to COVID-19 infection has shown a higher mortality than myocarditis related to mRNA vaccination. Before the COVID-19 vaccine were [sic] available, the incidence and extent of myocardial injury associated with COVID-19 infection was [sic] much higher than observed in this active surveillance study after booster vaccination. One of the Mueller co-authors had commercial ties to diagnostics companies. Another had previously been compensated by diagnostics and vaccine manufacturers. Mueller had relationships with diagnostics, pharmaceutical and vaccine companies at the time he wrote the paper. Where did Mueller go wrong? One way to measure treatment effects is to compare an outcome, for example, blood pressure, in the same subjects before and after the treatment and report before-and-after results. Although this option was known to medical researchers and available to him, Mueller did not take advantage of it — either because he did not think to measure pre-booster troponin levels or chose not to report them for some reason, perhaps because they did not align with his other results. Instead, his team took an approach that required two well-matched study groups. Although Mueller claimed placebos and controls met this requirement they differed on the feature that mattered most: heart health. Vaccinated subjects with current or recent heart issues were excluded from the study, while all control subjects had just entered the hospital with heart symptoms and were therefore already at greater risk for myocarditis. Klement and Walach found more anomalies in the Mueller paper. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now They began their critique by citing three 2021 studies on COVID-19 vaccine-induced myocarditis (here, here and here). All three studies showed myocarditis became a concern shortly after the COVID-19 vaccine introductions. They discussed three papers in some detail: A 2023 German autopsy study on 25 unexpected deaths within 20 days of COVID-19 vaccination identified acute myocarditis as the most probable cause of death in four cases. A 2023 report on myocarditis in 303 non-vaccinated and 700 vaccinated asymptomatic subjects found significantly higher damage in the vaccinated persisting for up to 180 days post-vaccination. One of the first autopsy papers, an Indian-led study based on World Health Organization pharmacovigilance data reported 2.1 times the risk for cardiac arrest, 2.7 times the risk for acute heart attack, 2.6 times the risk for elevated troponin, and 7.3-fold higher levels of D-dimer for COVID-19 vaccinations compared with the use of other medications. These studies strongly suggest that myocarditis became an issue only after the mRNA vaccine rollouts. They contradict Mueller’s statement that the “extent of myocardial injury associated with COVID-19 infection was much higher than observed in this active surveillance study after booster vaccination.” According to Klement and Walach, this statement is wrong for two reasons. First, in addition to the non-equivalence of controls’ and subjects’ heart-health status, Mueller ignored the much larger number of COVID-19-infected, unhospitalized, unvaccinated individuals with (presumably) much lower troponin levels compared with patients entering the hospital with heart symptoms. Second, Klement and Walach argued that the public health impact of myocarditis depends not only on the incidence or rate among study groups but the size of those groups. The significance is that a lower incidence in a very large group (vaccinated) is more meaningful than a slightly higher rate in a very small group (individuals infected with COVID-19). scales of justice Your support helps fund this work, and CHD’s related advocacy, education and scientific research. Donate Now On that basis, Klement and Walach estimated the number of myocarditis cases among all German COVID-19 hospitalizations at 27,467, and among those who were vaccinated at 1.97 million. As a result, regardless of myocarditis severity, there were 71.7 times as many myocarditis cases among the vaccinated as among those hospitalized for COVID-19. A similar analysis for Switzerland estimated 169,960 cases of myocarditis among vaccinated compared with 8,179 among those hospitalized for COVID-19. Although not as dramatic as the German estimates this still shows a much higher occurrence of heart damage among vaccinated versus hospitalized. In a June 2021 paper, Walach, Klement and Dutch data analyst Wouter Aukema concluded that based on 700 adverse reactions, 16 serious side effects and 4.11 deaths for every 100,000 vaccinations, COVID-19 vaccines were released with insufficient safety data. The authors said the risk-benefit ratio for mRNA vaccines did not add up because “for three deaths prevented by vaccination we have to accept two inflicted by vaccination.” Mueller told The Defender via email: “Our study reveals an important lack of prospective safety data concerning COVID-19 vaccines. Given the magnitude of the vaccinated population compared to the much smaller proportion of the population that became infected and developed symptoms, including a small percentage with possible heart damage, our findings should remain qualitatively robust.” LEARN MORE ⬇️ https://childrenshealthdefense.org/defender/covid-study-myocarditis-vaccines/ Join ➡️ @ShankaraChetty
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    Study Claims COVID Caused More Heart Damage Than Vaccines — Here’s What the Authors Got Wrong
    A 2023 study admitted that the COVID-19 mRNA vaccines cause myocarditis, but claimed the COVID-19 virus was even more damaging than the vaccine. A recent, more detailed review of their data, however, showed the opposite is likely true.
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  • FREEMASONRY & ZIONISM – 1. Apocalyptic “Cataclysms” by Synagogue of Satan | VT Foreign Policy
    February 24, 2024
    VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel

    $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts
    Source: Embassy of Israel, Washington, D.C. and US Department of State.

    “To the angel of the church in Smyrna write: These are the words of him who is the First and the Last, who died and came to life again. I know your afflictions and your poverty—yet you are rich! I know about the slander of those who say they are Jews and are not, but are a synagogue of Satan”.
    Saint John Apostle and Evangelist – Book of the Revelation (Rev. 2, 8-10)

    In the cover image the prime minister of the Israeli Zionist Regime Benjamin Nethanyau and the “Pope of Freemasonry” Albert Pike

    NB – some quotes of American persons have been translated from sources in Italian so forgive any stylistic errors or differences with the original ones

    By Fabio Giuseppe Carlo Carisio

    VERSIONE IN ITAIANO

    «The revelation from Jesus Christ, which God gave him to show his servants what must soon take place. He made it known by sending his angel to his servant John, who testifies to everything he saw—that is, the word of God and the testimony of Jesus Christ. Blessed is the one who reads aloud the words of this prophecy, and blessed are those who hear it and take to heart what is written in it, because the time is near».

    This Prologue to the Book of the Revelation (Apocalypse) of Saint John the Evangelist, the only Apostle who died without martyrdom as a reward for his loyalty to Jesus under the cross of Golgotha, reread in recent days, after almost a million deaths caused in recent years by the wars in Ukraine, Syria. Iraq and Libya (to name the best known) and after the genocide of the Israeli army in Palestine in which over 8 thousand children were massacred by bombs in a few weeks together with around 22 thousand adults, we should be inspired by a profound spiritual reflection also by virtue of the prophecy on Armageddon, the final battle of the armies foretold in the Holy Land in the same text on the Apocalypse which in Greek, it is good to remember it only means “revelation”, “prophecy” and not “catastrophe”.

    They take on an equally tragic meaning if we think of the holocaust of millions of victims caused both by the pandemic triggered by a SARS-Cov-2 built in the laboratory and by the killer vaccines with which unscrupulous Big Pharma is testing the world population like a massive human guinea-pig to reach the transhumanist goal of eugenic health culture: denial of Nature and the Almighty God of the Judeo-Christian tradition, which has survived 7 thousand years of attempts at annihilation.

    THE GENOCIDE OF THE PALESTINIANS AND THE HOLOCAUST OF THE VACCINATED

    Faced with this extraordinary “pande-medic holocaust” made invisible by the denialism of those who govern politics and science in obedience to the powers of the New World Order clearly theorized as an evolution of NATO by the Hungarian-American plutarch George Soros in 1993, the Palestinian victims , Ukrainian, Syrian conflicts caused precisely by military conflicts plotted by the Atlantic Alliance and by Anglo-Saxon intelligence appear as the ordinary, inevitable consequence of the hatred and ferocity that has plagued human history since the time of Cain. This name will come back later…

    Therefore, the biblical reference in the Book of Revelation to “those who proclaim themselves Jews and are not, but belong to the synagogue of Satan” does not appear in vain in the case of the Zionist leader Netanyahu who is carrying out a genocide of Palestinians after having mass vaccinated his fellow Israelis for a gigantic transversal business between the Weapons Lobby and Big Pharma with American President Joesph Biden.

    Modern telecommunications means – where not blocked as in Gaza to prevent reckless reporters from documenting the war crimes ordered by Israeli Prime Minister Benjamin Netanyahu already renamed “the Hitler of the 21st Century” by Turkish lawyers who demand his indictment – have made the bloody genocide tacitly legalized by the West and carried out in the churches and hospitals of Palestine terrifying, bringing before the eyes and ears cries that implore revenge and make the sense of forgiveness waver even in Christians, all this satanic torment appears comparable screams from the silence imploded in the hearts of children torn by lethal myocarditis or in the brains devoured by turbo-cancer of the victims of adverse reactions to the mRNA Covid vaccines.

    Precisely because their roar against death is silent, broken in the throat by a sudden illness of which political, health and judicial authorities too often do not want to detect and reveal traces of the FAILURE OF A SYSTEM. Precisely that of the New World Order which is seeking God’s mercy with the merciless human reason capable of killing an 8-month-old baby girl, Indi Gregory, although she had a concrete hope of being assisted.

    THE CATACLYSM FORECAST BY THE “POPE” OF AMERICAN FREEMASONRY

    If all this happening is not a coincidence but appears to be an international and historical conspiracy foreseen in very remote times by the American “Pope of Freemasonry”, a Southern general, about whom we have already written, who was among the Confederate supporters of the Civil War but also among the founders of the KuKluxKlan and among the followers of satanic rites: Albert Pike.

    We have already mentioned his extensive correspondence with the 33rd degree Freemason of the Supreme Council of the Ancient Accepted Scottish Rite Giuseppe Mazzini who, thanks to the financing of the hooded friends of the London lodges ready to host him even though he was a fugitive terrorist in Europe, planned the Expedition of the Thousand of Masonic guerrilla Giuseppe Garibaldi with whom the Kingdom of Italy wrested a part of Rome from the Papal State in the gigantic and crude plot against Christianity and the Catholic Church, partly attenuated only by the faith of the Ruling Savoy Dynasty.

    But we had missed some passages which in the light of today’s events take on monstrous relevance, furthermore proving the imprint of Freemasonry, like a Mark of the Beast, in every religious and political conflictual drift, prodigiously foreseen in detail by General Pike.

    In these first episodes we will analyze the conspiratorial complicity of Freemasonry with Zionism. In the next one with Nazism and Jihadist Islamism, where in a previous investigation we have analyzed the role of hooded men between Capitalism and Communism.

    «The Third World War will have to be fomented by taking advantage of the differences stirred up by the agents of the Illuminati between political Zionism and the leaders of the Islamic world. The war will have to be oriented so that Islam (including the State of Israel) destroy each other, while at the same time the remaining nations, once again divided and opposed to each other, will then be forced to fight each other until to complete physical, mental, spiritual and economic exhaustion».

    This is what Pike wrote to Mazzini on 15 August 1871 in a letter according to the revelations made by the commodore of the Canadian navy William Guy Carr which he later reported in his famous 1954 book Pawns in the Game. He stated that he learned about the letter from the anti-Mason, Cardinal José María Caro Rodríguez of Santiago, Chile, the author of The Mystery of Freemasonry Unveiled (Hawthorne, California, Christian Book Club of America, 1971).

    The Navy official can be considered very reliable as worked also for the Canadian Intelligence Service during World War II, and in 1944 he published Checkmate in the North, a book about an invasion by the Axis forces to take place in the area of the CFB Goose Bay (Canadian Forces Base Goose Bay).

    Carr’s books often discuss a Luciferian conspiracy by what he called the “World Revolutionary Movement,” but he later attributed the conspiracy more specifically to the “Synagogue of Satan.”

    The term was not a reference to Judaism as he wrote: “I wish to make it clearly and emphatically known that I do not believe the Synagogue of Satan (S.O.S.) is Jewish, but, as Christ told us for a definite purpose, it is comprised of ‘I know the blasphemy of them which say they are Jews, and are not, but are the synagogue of Satan.’ (Rev. 2:9 and 3:9)


    Albert Pike, the Pope of American Freemasonry
    The Canadian commodore reported what we had already mentioned in the previous investigation on Pike and which we will try to contextualize both in the biblical, esoteric and historical context in the following lines.

    «The First World War had to be fought to allow the “Illuminati” to overthrow the power of the czars in Russia and transform this country into the fortress of atheist communism. The differences stirred up by “Illuminati” agents between the British and German Empires were used to foment this war. After the war was over, communism had to be built and used to destroy other governments and weaken religions».

    Citing Confederate General Pike who was Grand Master of the Mother Lodge of Charleston (but also, in all probability, the only Southerner to have had, until recently, a statue in his memory in the USA sculpted by an Italian but recently destroyed by vandals), the commodore added:

    «The Second World War had to be fomented by taking advantage of the difference between fascists and political Zionists. The war had to be fought in order to destroy Nazism and increase the power of political Zionism, in order to allow the establishment of the sovereign state of Israel in Palestine. During the Second World War, a Communist International had to be established as strong as the whole of Christianity. At this point the latter had to be contained and kept under control until required for the final social cataclysm».

    Rereading these sentences after having published an investigation into the recent Israeli military plan for the genocide and forced exodus of Palestinians in Egypt and Europe represents a disturbing and burning confirmation but is not enough to understand the deepest motivations of the diabolical NWO conspiracy.

    On 15 August 1871, as revealed by Carr, the Pope of American Freemasonry Pike revealed to Mazzini that at the end of the Third World War those who aspire to World Government would cause the greatest social cataclysm ever seen.

    «We will unleash the nihilists and atheists and provoke a formidable social cataclysm which will clearly show, in all its horror, to the nations, the effect of absolute atheism, the origin of barbarism and bloody subversion».

    And then again:

    «Then everywhere citizens, forced to defend themselves against a world minority of revolutionaries, these destroyers of civilization, and the multitude disillusioned by Christianity, whose worshipers will be devoid of orientation in search of an ideal, will receive the true light through the universal manifestation of pure doctrine of Lucifer finally revealed to the public eye, a manifestation which will be followed by the destruction of Christianity and atheism conquered and crushed at the same time».

    GEOPOLITICAL ANALYSIS OF THE THIRD WORLD WAR IN FRAGMENTS

    If we carefully analyze what has happened in the last twenty years, rereading them with the lens of a geopolitical intelligence analysis, we can put together these dramatic events that prove the gradual increase of the Third World War “in a patchy pattern, in fragments, or in small pieces” as defined several times by Pope Francis.

    September 11, 2001 – From the World Trade Center to the War in Afghanistan

    Avoidable massacre of the attacks on the Twin Towers facilitated by the obstacles posed by the American counter-espionage of the Central Intelligence Agency (CIA) to the investigations of the director of anti-terrorism of the FBI John O’Neill (who died in the World Trade Center where he was hired after being fired following sabotage of his professional activity). The hidden role of the Israeli counter-intelligence Mossad came to light immediately, recently with the disconcerting confirmation that two of the hijackers were collaborating with the CIA.

    Thanks to that event, the USA, led by the Weapons Lobby controlled by investment funds of Zionist financiers such as Larry Fink, began the terrible and unsuccessful war in Afghanistan

    July 18, 2007 – Hamas conquers Gaza

    Palestinian President Abbas issued a decree outlawing the Hamas militias who defeated Fatah (a Palestinian political and paramilitary organization, part of the PLO, of which Yasser Arafat was leader) and therefore removed the Gaza Strip from the control of the Authority Palestinian national authority.

    According to various intelligence experts including a former CIA director, Hamas, linked to the Sunni Muslim Brotherhood (sons of another Masonic history…), was financed by the USA and Israel precisely to lead to the Palestinian exodus plan that was configured in recent days after the attacks of 7 October which took the highly expert Israeli secret services (Shin Bet, Mossad and the military Aman) by surprise.

    March 15, 2011 – Civil War in Syria

    The Syrian Civil War begins thanks to the Color Revolution financed by Soros and armed by the CIA’s MOM operation with the supply of TOW anti-tank missiles to extremist jihadist factions related to Al Qaeda.

    In 2014, ISIS founded by Caliph Al Baghdadi entered the war shortly after his liberation from Camp Bucca where he was detained by the US Army for terrorist activity in Iraq. He was believed to be a Mossad and CIA agent

    February 20, 2014 – Start of the War in Ukraine

    The second Orange Revolution financed by the Zionist Soros in Kiev explodes in all its violence due to the shooting of mysterious mercenary snipers on Ukrainian policemen and the crowd. It seems like a repeat of what the CIA hatched in 2002 in Caracas. The coup financed by NATO countries materializes with the escape of the legitimately elected president Viktor Fedorovyč Yanukovych to friendly Russia.

    From there begins the Donbass Civil War which became a Global Conflict after the start of Moscow’s military operation to protect the pro-Russian victims of genocide by the neo-Nazi guerrillas of the Azov Battalion led by the Kiev Regime and also armed by Israel in an apparent, crazy paradox …

    April 2014 – “Sabotaged” elections in Palestine

    Fatah and Hamas sign agreements in Gaza for the return to voting in all PNA territories, foreseeing elections for the following October.

    In July, however, the Israelis launched Operation Protective Edge to destroy clandestine tunnels into their country, triggering a resurgence of military clashes. Only on 28 August was a ceasefire declared by both sides but the electoral consultations were postponed and never agreed upon again.

    October 2023 – Genocide Planned and Legalized in Gaza

    Hamas captures hostages from an Israeli Rave Party and several kibbutz settlers in the illegally occupied territories. Israel responds disproportionately by bombing everyone, women, children, hospitals, churches, UN officials. Few Western politicians denounce a GENOCIDE which instead appears LEGALIZED by almost all NATO countries.

    If we correlate the recurring subjects of these events it is easy to deduce that the Third World War in fragments has already been implemented for at least two decades with an enormous occult direction of that NATO evoked by Soros to embody the New World Order.

    ANALYSIS OF THE SOCIAL CATALYSM: MANMADE VIRUS PANDEMIC

    Let’s go back to the tired “forecasts” of the Freemason Albert Pike and reread a significant phrase:

    «We will unleash the nihilists and atheists and provoke a formidable social cataclysm which will clearly show, in all its horror, to the nations, the effect of absolute atheism, the origin of barbarism and bloody subversion».

    Since 2001, the American virologist Anthony Fauci began playing with dangerous viruses manipulated in the laboratory as biological weapons thanks to enormous funding provided by both the Department of Health and Defense, including through Pentagon agencies such as DARPA.

    https://www.gospanews.net/en/2024/01/09/faucis-testimony-before-us-congress-uncovered-drastic-failures-in-public-health-systems-and-pandemic-origin/

    In 2004 the European Commission chaired by Romano Prodi, a Soros associate, financed the Wuhan Institute of Virology strengthened by the son of President Jiang Zemin, the Executioner of Tiananmen, also in light of an agreement on collaborations for research in the bacteriological field signed with the American president Bill Clinton in 1999.

    In December 2019 the first outbreak of SARS-Cov-2 was discovered in Wuhan and for over 2 years the USA blamed the Chinese while the scientific community of Fauci & Co. tried to cover up the artificial orgone ascertained by the Senate Health Commission and the House Investigation Committee of the US Congress only in 2023.

    Now even many US politicians admit their nation’s role in building the laboratory virus. This is denied by the National Intelligence Directorate led by Avril Haines who was deputy CIA director expert in bio-weapons when Fauci was carrying out experiments on Coronaviruses on behalf of the Obama-Biden administration together in Wuhan.

    European Union politicians continue to ignore or deny the artificial origin of the virus. While almost everyone has welcomed, so much so as to impose them as mandatory even for many professional categories, the experimental mRNA genetic serums based on the toxic Spike protein and promoted by a swirl of billionaire interests of Big Pharma with governments and the usual Zionist lobbies who also invest in Warlord corporations.

    Even the Catholic Church genuflects to the Vaccine GOD.

    Let’s reread Pike’s prophecy again, a truly disturbing name when associated with the almost homonymous Covid-19 protein.

    «Then everywhere citizens, forced to defend themselves against a world minority of revolutionaries, these destroyers of civilization, and the multitude disillusioned by Christianity, whose worshipers will be devoid of orientation in search of an ideal, will receive the true light through the universal manifestation of pure doctrine of Lucifer finally revealed to the public eye, a manifestation which will be followed by the destruction of Christianity and atheism conquered and crushed at the same Time»

    HISTORICAL ANALYSIS OF THE RELATIONSHIP BETWEEN FREEMASONRY AND ZIONISM

    The detractors of the military geopolitical analyst and writer William Guy Carr who refers to the diabolical plan of the Pope of American Freemasonry are based on the fact that Albert Pike in 1871 could not have known about the birth of Communism, nor of Nazism, nor of Zionism.

    Nor even knowing about the two world wars. Unless you were among those who designed them.

    This observation can easily be refuted by citing some historical references already mentioned and which we will highlight.

    «In July 1782 the Order of the Illuminati allied itself with Freemasonry during the Congress of Wilhelmsbad, which the historian Freemason Albert Mackey defined as ‘the most important Masonic Congress of the eighteenth century’ – we read on the website Freemasonry Unmasked, full of anecdotes and authoritative historical sources – The participants in that Congress had to swear not to reveal the decisions they had made to anyone (see Nesta H. Webster, World Revolution, 1921, page 31)».

    Wilhelmsbad Castle was owned by the Ashkenazi Jewish banker (of Khazar-European origins) Mayer Amschel Rothschild who, according to various historians, in 1777 brought together twelve of his most influential friends and convinced them that if they pooled their resources they could dominate the world: this is how the Bavarian Illuminati was born.

    The French Revolution confirms their success with the annihilation of the first important Catholic Monarchy. It will be the experience of the Paris Commune of 1871, the regurgitation of the regime of terror, that will inspire Lenin in his plan for the subsequent Bolshevik and Communist revolution.

    So Pike was not only still alive at the time but knew the details.

    The Independent Order B’nai B’rith or Bené Berith (Hebrew: בני ברית, “sons of the covenant”) is a Jewish lodge founded in 1843 during the presidency of John Tyler and still existing and active. It was founded at the Sinsheimer Café, in the Wall Street neighborhood of New York, by Henry Jones and eleven other people on October 13, 1843. The original name was in German “Bundes-Brueder” (which means “League of Brothers”), in the current one which retains the initials (“BB”).

    Most of the founders were German-Jews: that is, Ashkenazi like Mayer Amschel Rothschild but also like his descendant Walter Rothschild, eldest son and heir of the banker Nathan Mayer Rothschild, the first Jewish baron of England.

    Walter Rothschild was among the promoters of the declaration for the formation of the Jewish state in Palestine, later earning the merit of becoming president of the Council of Deputies of British Jews from 1925 to 1926.

    From these seeds we arrived at 1917 when a letter from the British Foreign Minister Arthur Balfour, addressed to the “Dear Lord Rothschild”, sanctioned Balfour’s declaration which committed the British government to supporting the creation in Palestine of a home for the Jews in respect for the rights of other resident minorities.

    How did Albert Pike know all these things before they happened?

    Very simple because he was among those who concerted them in 1860 when the Southern general through Young America planned the American Civil War to defend the right to slavery, Mazzini with Young Italy committed himself to the Expedition of the Thousand and Henry John Temple, 3rd Viscount of Palmerston, British Secretary of State and exponent of the Grand Lodge of England guaranteed all financial and political support.

    The first expressions of proto-Zionism took shape, for example, in the foundation of the Universal Israelite Alliance in 1860, an organization aimed at the emancipation of the Jewish communities in the Middle East and North Africa, and in the publication of various works, including Rome and Jerusalem, written in 1862 by the German Jewish philosopher Moses Hess, Derishat Zion by the Polish-Prussian rabbi Zvi Hirsch Kalischer, and the hymn Hatikvah, whose lyrics were written by Naftali Herz Imber and which later became the anthem of the State of Israel.

    Zionism draws its roots from the new cultural environment generated in the context of the emancipation of European Jews starting from the French Revolution and throughout the 19th century and from the Haskalah.

    The haskalah, with a small delay compared to other Enlightenment movements, arose in Germany and then spread throughout much of Europe and to a small extent also across the Atlantic. The father and inspirer of the movement was Moses Mendelssohn, close to Gotthold Ephraim Lessing, a free thinker of Protestant extraction and an energetic defender of the Jews in Germany. The latter introduced Mendelssohn into the world of Berlin intellectuals where he dedicated himself to the composition of philosophical essays and dissertations.

    A varied and open movement, the haskalah probably did not close its doors even to exponents of the Frankist heresy, a sort of tail of the messianic movement of Shabatai Zevi which had long been in opposition to official Judaism, perhaps linked to lodges of freemasonry, another force of the times, definitely in relation to the Enlightenment philosophy.

    Many Jews influenced by the haskalah and the closeness it brought with European culture were seduced by the possibility of assimilation by embracing Christianity. Just think of the family of Karl Marx, descended from rabbis who converted to Protestantism, as did Mendelssohn’s own daughters. Others, however, laid the foundations of the new science of Judaism, the Wissenschaft des Judentums.

    THE LODGES INSPIRED BY THE SON OF THE BIBLICAL MURDERER CAIN

    In the previous investigation we highlighted how Marx received the task of writing Capital from British Freemasonry. In other reports we have highlighted the fundamental role played by the Protestants in the birth of the Grand Lodge of London on 24 June 1717.

    Today we add another detail by recalling the figure of John Theophilus Desaguliers (La Rochelle, 12 March 1683 – Covent Garden, 29 February 1744) who was an English scientist, religious and Freemason of French origins.

    Desaguliers emigrated to England in 1694, due to the Edict of Fontainebleau, which revoked the freedom of worship of Protestants. He approached Freemasonry, becoming Grand Master of the First Grand Lodge of England in 1718, and Deputy Grand Master in 1723 and 1725. Under his leadership, the Grand Lodge of London and Freemasonry developed in an “astonishing” way in the islands British, to the point that «in 1740 there were already more than 180 lodges».

    Each of the earliest Masonic texts contains some sort of history of the craft, or guild, of Freemasonry. The oldest work of this type, the Royal Manuscript, dating from 1390 to 1425, has a brief history in the introduction, which states that the “craft of Freemasonry” began with Euclid in Egypt, and arrived in England during the reign of ruler Æðelstan.

    A little later, the Cooke Manuscript traces Freemasonry to Jabal, son of Lamech (Genesis 4, 20-22), and tells how this knowledge reached Euclid, from him to the children of Israel when they were in Egypt, and so on for an elaborate route to Æðelstan. This myth formed the basis for later manuscript foundations, all of which claim that Freemasonry dates back to Biblical times, and pegs its institutional consolidation in England during the reign of Æðelstan (927-939).

    Shortly after the formation of the first Grand Lodge of England, James Anderson was commissioned to summarize these “Gothic constitutions” into a pleasing modern form. The constitutions produced by his work have a more widespread historical introduction than any previous one, and once again connect the history of what Freemasonry had become to its biblical roots, always inserting Euclid into the chain of narrative.

    The first question that a connoisseur of Judeo-Christian history should ask is almost banal.

    Why do the Freemasons, due to fabulous legendary and historical beliefs, trace Freemasonry to one of the descendants of the murderer Cain and not to the third son of Adam named Set from whom the Semitic culture was born?

    In this, the manipulation carried out over the centuries by Rabbinic Taldumist Judaism, well described by the Judaism expert Professor Paola Persichetti in the previous investigations in which she highlights the correlations of this Jewish regurgitation following the Destruction of the Temple of Jerusalem, seems evident.

    In France, Chevalier (Knight) Ramsay’s 1737 conference added Crusader Freemasons to the family tree claiming that they had revived the craft with secrets recovered in the Holy Land, under the patronage of the Knights Hospitaller. At this point, the “history” of the profession of continental Freemasonry separated from that of Freemasonry in England which in the meantime had published its “charter”.

    THE SCHSM ON THE GREAT ARCHITECT OF THE UNIVERSE

    The Constitutions of the Free-Masons, “for the use of the lodges” in London and Westminster, was published in 1723. It was edited by the Presbyterian clergyman James Anderson, by order of John Theophilus Desaguliers, and approved by a committee of the grand lodge under its control. The work was reprinted in Philadelphia in 1734 by Benjamin Franklin, who in that year became Grand Master of the Pennsylvania Freemasons. It was also translated into Dutch (1736), German (1741) and French (1745).

    Anderson was minister of the Presbyterian church in Swallow Street, London, which had formerly been a Huguenot church, and whose pastor in the 1690s was Desaguliers’ father. At the time of his meeting with Desaguliers, he appears to have presented himself as a Talmudic scholar.

    In various historical testimonies that we summarize for brevity, Anderson himself seems to imply the existence of an Italian Grand Lodge.

    In Naples in 1728 he saw the light of the first regular Masonic lodge established in Italy, La Perfetta Unione. Raised by the will of the Prince of San Severo, it had Egyptian symbols such as the pyramid, the Sphinx and the radiant sun in its emblem. Subsequently, the English lodge (“La Loggia degli Inglesi”) was established in Florence, founded in 1731 and Freemasonry spread rapidly, despite a series of papal prohibitions.

    But already ahead the so-called Great Schism occurred. According to a widespread opinion, the schism between French and English Freemasonry originates from the general assembly of the Grand Orient of France in September 1877. Accepting the recommendation contained in a report by the Protestant pastor (and Freemason) Frédéric Desmons, the assembly decided by a majority of amend its constitutions by inserting the formula “its principles are absolute freedom of conscience and human solidarity”. This replaced the previous statement “its principles are the existence of God, the immortality of the soul and human solidarity”.

    The reaction of the United Grand Lodge of England (UGLE) was the resolution of March 1878 which reiterated “That the Grand Lodge, while anxious to welcome in the most fraternal spirit the Brethren of any foreign Grand Lodge whose proceedings are conducted according to the Ancient cornerstones of the Order, among which the first and most important is the faith in T. G. A. O. T. U. [“the great Architect of the universe”, in English acronym], cannot recognize as ‘true and genuine’ Brothers all those who have been initiated in lodges that deny or ignore that faith.”

    FREEMASONRY SIMILAR TO THE BEAST OF THE APOCALYPSE

    Having concluded this long but necessary historical digression on Freemasonry implemented with various Wikipedia sources, let’s return to the beginning. To the book of the Apocalypse of Saint John and the disturbing esoteric symbolisms.

    If we summarize the historical notes above we can easily conclude that the first promoters of Zionism in the USA were the founders of the B’nai B’rith Lodge composed of Ashkenazi Jews (as Adolph Hitler is also believed to be) that the historians of Jewish culture they define the “13th Tribe of Israel” as they derive from the diaspora of the Khazars who had converted to Judaism for purely political reasons.

    While in Europe it spread thanks to the Rothschild Dynasty (Red Shield) which was the first to weave subversive plots with an anti-Catholic vocation from the birth of the Bavarian Illuminati up to the pact of terror for the French Revolution from which the liberation of the proto- Zionism together with that Masonic concept of “Liberté, Égalité, Fraternité” imposed by guillotining even the elderly nobles of the Catholic Vendée French region.

    In light of all this, the words of the Satanist Albert Pike, Pope of American Freemasonry, take on an iconic relevance in the common project between Masonic and Zionist Lodges for the New World Order:

    «Then everywhere citizens, forced to defend themselves against a world minority of revolutionaries, these destroyers of civilization, and the multitude disillusioned by Christianity, whose worshipers will be devoid of orientation in search of an ideal, will receive the true light through the universal manifestation of pure doctrine of Lucifer finally revealed to the public eye, a manifestation which will be followed by the destruction of Christianity and atheism conquered and crushed at the same time».

    But following this hermeneutical path to the Book of the Apocalypse, one of the most important allegories comes to mind with disconcerting and terrifying impetus:

    «The dragon stood on the shore of the sea. And I saw a beast coming out of the sea. It had ten horns and seven heads, with ten crowns on its horns, and on each head a blasphemous name. The beast I saw resembled a leopard, but had feet like those of a bear and a mouth like that of a lion. The dragon gave the beast his power and his throne and great authority. One of the heads of the beast seemed to have had a fatal wound, but the fatal wound had been healed. The whole world was filled with wonder and followed the beast. People worshiped the dragon because he had given authority to the beast, and they also worshiped the beast and asked, “Who is like the beast? Who can wage war against it?» (Rev. 13, 1-4)

    The prophet Saint John the Apostle and Evangelist delves into the concept with an aura vision

    «Then I saw a second beast, coming out of the earth. It had two horns like a lamb, but it spoke like a dragon. It exercised all the authority of the first beast on its behalf, and made the earth and its inhabitants worship the first beast, whose fatal wound had been healed» (Rev. 13, 11-12)

    It is not really scary to note how traditional esoteric Freemasonry became manifest thanks to the Anglican political schism of the Protestants and allowed Pharisaic Judaism, defeated by the Diaspora after the Crucifixion of the Messiah awaited by the Jews, to be reborn in its Talmudic form with Judaism then became with Zionism the most powerful component of the New World Order?

    We have historical clues that help identify Freemasonry as one of the two apocalyptic Beasts. But this theme will be explored in greater depth if and when we receive from the Holy Spirit the gift of the wisdom necessary to interpret it. Therefore today we cannot help but insinuate doubt…

    POWER OF CHRIST IN THE PROPHECY OF SAINT JOHN THE APOSTLE

    But it is precisely Chapter 12 of the Book of the Apocalypse (Rev. 12, 7-12) which comes to illuminate with a radiant dawn of hope the dangers of all of us Christians who strive to be among those “who listen to the words of this prophecy and put into practice the things that are written in it”:

    «Then war broke out in heaven. Michael and his angels fought against the dragon, and the dragon and his angels fought back. But he was not strong enough, and they lost their place in heaven. The great dragon was hurled down—that ancient serpent called the devil, or Satan, who leads the whole world astray. He was hurled to the earth, and his angels with him».

    Then I heard a loud voice in heaven say:

    “Now have come the salvation and the power
    and the kingdom of our God,
    and the authority of his Messiah.
    For the accuser of our brothers and sisters,
    who accuses them before our God day and night,
    has been hurled down.
    They triumphed over him
    by the blood of the Lamb
    and by the word of their testimony;
    they did not love their lives so much
    as to shrink from death.
    Therefore rejoice, you heavens
    and you who dwell in them!
    But woe to the earth and the sea,
    because the devil has gone down to you!
    He is filled with fury,
    because he knows that his time is short.”

    Since Saint John was the only Apostle who died without martyrdom for his loyalty to Jesus Christ under the cross and also survived the hell of imprisonment on Patmos (where he received the visions and locutions collected in the Apocalypse), it is probably very useful to start believing him…

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    BOOK OF REVELATION (APOCALYPSE) – HOLY BIBLE

    Epiphanius – Massoneria e sette segrete, Controcorrente Edizioni, pag. 163, 164, 165, 166. – Citazioni da I Nuovi Vespri

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    Fabio G. C. Carisio
    Fabio is investigative journalist since 1991. Now geopolitics, intelligence, military, SARS-Cov-2 manmade, NWO expert and Director-founder of Gospa News: a Christian Information Journal.

    His articles were published on many international media and website as SouthFront, Reseau International, Sputnik Italia, United Nation Association Westminster, Global Research, Kolozeg and more…

    Most popolar investigation on VT is:

    Rumsfeld Shady Heritage in Pandemic: GILEAD’s Intrigues with WHO & Wuhan Lab. Bio-Weapons’ Tests with CIA & Pentagon

    Fabio Giuseppe Carlo Carisio, born on 24/2/1967 in Borgosesia, started working as a reporter when he was only 19 years old in the alpine area of Valsesia, Piedmont, his birth region in Italy. After studying literature and history at the Catholic University of the Sacred Heart in Milan, he became director of the local newspaper Notizia Oggi Vercelli and specialized in judicial reporting.

    For about 15 years he is a correspondent from Northern Italy for the Italian newspapers Libero and Il Giornale, also writing important revelations on the Ustica massacre, a report on Freemasonry and organized crime.

    With independent investigations, he collaborates with Carabinieri and Guardia di Finanza in important investigations that conclude with the arrest of Camorra entrepreneurs or corrupt politicians.

    In July 2018 he found the counter-information web media Gospa News focused on geopolitics, terrorism, Middle East, and military intelligence.

    In 2020 published the book, in Italian only, WUHAN-GATES – The New World Order Plot on SARS-Cov-2 manmade focused on the cycle of investigations Wuhan-Gates

    His investigations was quoted also by The Gateway Pundit, Tasnim and others

    He worked for many years for the magazine Art & Wine as an art critic and curator.

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    https://www.vtforeignpolicy.com/2024/02/freemasonry-zionism-1-apocalyptic-cataclysms-by-synagogue-of-satan/
    FREEMASONRY & ZIONISM – 1. Apocalyptic “Cataclysms” by Synagogue of Satan | VT Foreign Policy February 24, 2024 VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts Source: Embassy of Israel, Washington, D.C. and US Department of State. “To the angel of the church in Smyrna write: These are the words of him who is the First and the Last, who died and came to life again. I know your afflictions and your poverty—yet you are rich! I know about the slander of those who say they are Jews and are not, but are a synagogue of Satan”. Saint John Apostle and Evangelist – Book of the Revelation (Rev. 2, 8-10) In the cover image the prime minister of the Israeli Zionist Regime Benjamin Nethanyau and the “Pope of Freemasonry” Albert Pike NB – some quotes of American persons have been translated from sources in Italian so forgive any stylistic errors or differences with the original ones By Fabio Giuseppe Carlo Carisio VERSIONE IN ITAIANO «The revelation from Jesus Christ, which God gave him to show his servants what must soon take place. He made it known by sending his angel to his servant John, who testifies to everything he saw—that is, the word of God and the testimony of Jesus Christ. Blessed is the one who reads aloud the words of this prophecy, and blessed are those who hear it and take to heart what is written in it, because the time is near». This Prologue to the Book of the Revelation (Apocalypse) of Saint John the Evangelist, the only Apostle who died without martyrdom as a reward for his loyalty to Jesus under the cross of Golgotha, reread in recent days, after almost a million deaths caused in recent years by the wars in Ukraine, Syria. Iraq and Libya (to name the best known) and after the genocide of the Israeli army in Palestine in which over 8 thousand children were massacred by bombs in a few weeks together with around 22 thousand adults, we should be inspired by a profound spiritual reflection also by virtue of the prophecy on Armageddon, the final battle of the armies foretold in the Holy Land in the same text on the Apocalypse which in Greek, it is good to remember it only means “revelation”, “prophecy” and not “catastrophe”. They take on an equally tragic meaning if we think of the holocaust of millions of victims caused both by the pandemic triggered by a SARS-Cov-2 built in the laboratory and by the killer vaccines with which unscrupulous Big Pharma is testing the world population like a massive human guinea-pig to reach the transhumanist goal of eugenic health culture: denial of Nature and the Almighty God of the Judeo-Christian tradition, which has survived 7 thousand years of attempts at annihilation. THE GENOCIDE OF THE PALESTINIANS AND THE HOLOCAUST OF THE VACCINATED Faced with this extraordinary “pande-medic holocaust” made invisible by the denialism of those who govern politics and science in obedience to the powers of the New World Order clearly theorized as an evolution of NATO by the Hungarian-American plutarch George Soros in 1993, the Palestinian victims , Ukrainian, Syrian conflicts caused precisely by military conflicts plotted by the Atlantic Alliance and by Anglo-Saxon intelligence appear as the ordinary, inevitable consequence of the hatred and ferocity that has plagued human history since the time of Cain. This name will come back later… Therefore, the biblical reference in the Book of Revelation to “those who proclaim themselves Jews and are not, but belong to the synagogue of Satan” does not appear in vain in the case of the Zionist leader Netanyahu who is carrying out a genocide of Palestinians after having mass vaccinated his fellow Israelis for a gigantic transversal business between the Weapons Lobby and Big Pharma with American President Joesph Biden. Modern telecommunications means – where not blocked as in Gaza to prevent reckless reporters from documenting the war crimes ordered by Israeli Prime Minister Benjamin Netanyahu already renamed “the Hitler of the 21st Century” by Turkish lawyers who demand his indictment – have made the bloody genocide tacitly legalized by the West and carried out in the churches and hospitals of Palestine terrifying, bringing before the eyes and ears cries that implore revenge and make the sense of forgiveness waver even in Christians, all this satanic torment appears comparable screams from the silence imploded in the hearts of children torn by lethal myocarditis or in the brains devoured by turbo-cancer of the victims of adverse reactions to the mRNA Covid vaccines. Precisely because their roar against death is silent, broken in the throat by a sudden illness of which political, health and judicial authorities too often do not want to detect and reveal traces of the FAILURE OF A SYSTEM. Precisely that of the New World Order which is seeking God’s mercy with the merciless human reason capable of killing an 8-month-old baby girl, Indi Gregory, although she had a concrete hope of being assisted. THE CATACLYSM FORECAST BY THE “POPE” OF AMERICAN FREEMASONRY If all this happening is not a coincidence but appears to be an international and historical conspiracy foreseen in very remote times by the American “Pope of Freemasonry”, a Southern general, about whom we have already written, who was among the Confederate supporters of the Civil War but also among the founders of the KuKluxKlan and among the followers of satanic rites: Albert Pike. We have already mentioned his extensive correspondence with the 33rd degree Freemason of the Supreme Council of the Ancient Accepted Scottish Rite Giuseppe Mazzini who, thanks to the financing of the hooded friends of the London lodges ready to host him even though he was a fugitive terrorist in Europe, planned the Expedition of the Thousand of Masonic guerrilla Giuseppe Garibaldi with whom the Kingdom of Italy wrested a part of Rome from the Papal State in the gigantic and crude plot against Christianity and the Catholic Church, partly attenuated only by the faith of the Ruling Savoy Dynasty. But we had missed some passages which in the light of today’s events take on monstrous relevance, furthermore proving the imprint of Freemasonry, like a Mark of the Beast, in every religious and political conflictual drift, prodigiously foreseen in detail by General Pike. In these first episodes we will analyze the conspiratorial complicity of Freemasonry with Zionism. In the next one with Nazism and Jihadist Islamism, where in a previous investigation we have analyzed the role of hooded men between Capitalism and Communism. «The Third World War will have to be fomented by taking advantage of the differences stirred up by the agents of the Illuminati between political Zionism and the leaders of the Islamic world. The war will have to be oriented so that Islam (including the State of Israel) destroy each other, while at the same time the remaining nations, once again divided and opposed to each other, will then be forced to fight each other until to complete physical, mental, spiritual and economic exhaustion». This is what Pike wrote to Mazzini on 15 August 1871 in a letter according to the revelations made by the commodore of the Canadian navy William Guy Carr which he later reported in his famous 1954 book Pawns in the Game. He stated that he learned about the letter from the anti-Mason, Cardinal José María Caro Rodríguez of Santiago, Chile, the author of The Mystery of Freemasonry Unveiled (Hawthorne, California, Christian Book Club of America, 1971). The Navy official can be considered very reliable as worked also for the Canadian Intelligence Service during World War II, and in 1944 he published Checkmate in the North, a book about an invasion by the Axis forces to take place in the area of the CFB Goose Bay (Canadian Forces Base Goose Bay). Carr’s books often discuss a Luciferian conspiracy by what he called the “World Revolutionary Movement,” but he later attributed the conspiracy more specifically to the “Synagogue of Satan.” The term was not a reference to Judaism as he wrote: “I wish to make it clearly and emphatically known that I do not believe the Synagogue of Satan (S.O.S.) is Jewish, but, as Christ told us for a definite purpose, it is comprised of ‘I know the blasphemy of them which say they are Jews, and are not, but are the synagogue of Satan.’ (Rev. 2:9 and 3:9) Albert Pike, the Pope of American Freemasonry The Canadian commodore reported what we had already mentioned in the previous investigation on Pike and which we will try to contextualize both in the biblical, esoteric and historical context in the following lines. «The First World War had to be fought to allow the “Illuminati” to overthrow the power of the czars in Russia and transform this country into the fortress of atheist communism. The differences stirred up by “Illuminati” agents between the British and German Empires were used to foment this war. After the war was over, communism had to be built and used to destroy other governments and weaken religions». Citing Confederate General Pike who was Grand Master of the Mother Lodge of Charleston (but also, in all probability, the only Southerner to have had, until recently, a statue in his memory in the USA sculpted by an Italian but recently destroyed by vandals), the commodore added: «The Second World War had to be fomented by taking advantage of the difference between fascists and political Zionists. The war had to be fought in order to destroy Nazism and increase the power of political Zionism, in order to allow the establishment of the sovereign state of Israel in Palestine. During the Second World War, a Communist International had to be established as strong as the whole of Christianity. At this point the latter had to be contained and kept under control until required for the final social cataclysm». Rereading these sentences after having published an investigation into the recent Israeli military plan for the genocide and forced exodus of Palestinians in Egypt and Europe represents a disturbing and burning confirmation but is not enough to understand the deepest motivations of the diabolical NWO conspiracy. On 15 August 1871, as revealed by Carr, the Pope of American Freemasonry Pike revealed to Mazzini that at the end of the Third World War those who aspire to World Government would cause the greatest social cataclysm ever seen. «We will unleash the nihilists and atheists and provoke a formidable social cataclysm which will clearly show, in all its horror, to the nations, the effect of absolute atheism, the origin of barbarism and bloody subversion». And then again: «Then everywhere citizens, forced to defend themselves against a world minority of revolutionaries, these destroyers of civilization, and the multitude disillusioned by Christianity, whose worshipers will be devoid of orientation in search of an ideal, will receive the true light through the universal manifestation of pure doctrine of Lucifer finally revealed to the public eye, a manifestation which will be followed by the destruction of Christianity and atheism conquered and crushed at the same time». GEOPOLITICAL ANALYSIS OF THE THIRD WORLD WAR IN FRAGMENTS If we carefully analyze what has happened in the last twenty years, rereading them with the lens of a geopolitical intelligence analysis, we can put together these dramatic events that prove the gradual increase of the Third World War “in a patchy pattern, in fragments, or in small pieces” as defined several times by Pope Francis. September 11, 2001 – From the World Trade Center to the War in Afghanistan Avoidable massacre of the attacks on the Twin Towers facilitated by the obstacles posed by the American counter-espionage of the Central Intelligence Agency (CIA) to the investigations of the director of anti-terrorism of the FBI John O’Neill (who died in the World Trade Center where he was hired after being fired following sabotage of his professional activity). The hidden role of the Israeli counter-intelligence Mossad came to light immediately, recently with the disconcerting confirmation that two of the hijackers were collaborating with the CIA. Thanks to that event, the USA, led by the Weapons Lobby controlled by investment funds of Zionist financiers such as Larry Fink, began the terrible and unsuccessful war in Afghanistan July 18, 2007 – Hamas conquers Gaza Palestinian President Abbas issued a decree outlawing the Hamas militias who defeated Fatah (a Palestinian political and paramilitary organization, part of the PLO, of which Yasser Arafat was leader) and therefore removed the Gaza Strip from the control of the Authority Palestinian national authority. According to various intelligence experts including a former CIA director, Hamas, linked to the Sunni Muslim Brotherhood (sons of another Masonic history…), was financed by the USA and Israel precisely to lead to the Palestinian exodus plan that was configured in recent days after the attacks of 7 October which took the highly expert Israeli secret services (Shin Bet, Mossad and the military Aman) by surprise. March 15, 2011 – Civil War in Syria The Syrian Civil War begins thanks to the Color Revolution financed by Soros and armed by the CIA’s MOM operation with the supply of TOW anti-tank missiles to extremist jihadist factions related to Al Qaeda. In 2014, ISIS founded by Caliph Al Baghdadi entered the war shortly after his liberation from Camp Bucca where he was detained by the US Army for terrorist activity in Iraq. He was believed to be a Mossad and CIA agent February 20, 2014 – Start of the War in Ukraine The second Orange Revolution financed by the Zionist Soros in Kiev explodes in all its violence due to the shooting of mysterious mercenary snipers on Ukrainian policemen and the crowd. It seems like a repeat of what the CIA hatched in 2002 in Caracas. The coup financed by NATO countries materializes with the escape of the legitimately elected president Viktor Fedorovyč Yanukovych to friendly Russia. From there begins the Donbass Civil War which became a Global Conflict after the start of Moscow’s military operation to protect the pro-Russian victims of genocide by the neo-Nazi guerrillas of the Azov Battalion led by the Kiev Regime and also armed by Israel in an apparent, crazy paradox … April 2014 – “Sabotaged” elections in Palestine Fatah and Hamas sign agreements in Gaza for the return to voting in all PNA territories, foreseeing elections for the following October. In July, however, the Israelis launched Operation Protective Edge to destroy clandestine tunnels into their country, triggering a resurgence of military clashes. Only on 28 August was a ceasefire declared by both sides but the electoral consultations were postponed and never agreed upon again. October 2023 – Genocide Planned and Legalized in Gaza Hamas captures hostages from an Israeli Rave Party and several kibbutz settlers in the illegally occupied territories. Israel responds disproportionately by bombing everyone, women, children, hospitals, churches, UN officials. Few Western politicians denounce a GENOCIDE which instead appears LEGALIZED by almost all NATO countries. If we correlate the recurring subjects of these events it is easy to deduce that the Third World War in fragments has already been implemented for at least two decades with an enormous occult direction of that NATO evoked by Soros to embody the New World Order. ANALYSIS OF THE SOCIAL CATALYSM: MANMADE VIRUS PANDEMIC Let’s go back to the tired “forecasts” of the Freemason Albert Pike and reread a significant phrase: «We will unleash the nihilists and atheists and provoke a formidable social cataclysm which will clearly show, in all its horror, to the nations, the effect of absolute atheism, the origin of barbarism and bloody subversion». Since 2001, the American virologist Anthony Fauci began playing with dangerous viruses manipulated in the laboratory as biological weapons thanks to enormous funding provided by both the Department of Health and Defense, including through Pentagon agencies such as DARPA. https://www.gospanews.net/en/2024/01/09/faucis-testimony-before-us-congress-uncovered-drastic-failures-in-public-health-systems-and-pandemic-origin/ In 2004 the European Commission chaired by Romano Prodi, a Soros associate, financed the Wuhan Institute of Virology strengthened by the son of President Jiang Zemin, the Executioner of Tiananmen, also in light of an agreement on collaborations for research in the bacteriological field signed with the American president Bill Clinton in 1999. In December 2019 the first outbreak of SARS-Cov-2 was discovered in Wuhan and for over 2 years the USA blamed the Chinese while the scientific community of Fauci & Co. tried to cover up the artificial orgone ascertained by the Senate Health Commission and the House Investigation Committee of the US Congress only in 2023. Now even many US politicians admit their nation’s role in building the laboratory virus. This is denied by the National Intelligence Directorate led by Avril Haines who was deputy CIA director expert in bio-weapons when Fauci was carrying out experiments on Coronaviruses on behalf of the Obama-Biden administration together in Wuhan. European Union politicians continue to ignore or deny the artificial origin of the virus. While almost everyone has welcomed, so much so as to impose them as mandatory even for many professional categories, the experimental mRNA genetic serums based on the toxic Spike protein and promoted by a swirl of billionaire interests of Big Pharma with governments and the usual Zionist lobbies who also invest in Warlord corporations. Even the Catholic Church genuflects to the Vaccine GOD. Let’s reread Pike’s prophecy again, a truly disturbing name when associated with the almost homonymous Covid-19 protein. «Then everywhere citizens, forced to defend themselves against a world minority of revolutionaries, these destroyers of civilization, and the multitude disillusioned by Christianity, whose worshipers will be devoid of orientation in search of an ideal, will receive the true light through the universal manifestation of pure doctrine of Lucifer finally revealed to the public eye, a manifestation which will be followed by the destruction of Christianity and atheism conquered and crushed at the same Time» HISTORICAL ANALYSIS OF THE RELATIONSHIP BETWEEN FREEMASONRY AND ZIONISM The detractors of the military geopolitical analyst and writer William Guy Carr who refers to the diabolical plan of the Pope of American Freemasonry are based on the fact that Albert Pike in 1871 could not have known about the birth of Communism, nor of Nazism, nor of Zionism. Nor even knowing about the two world wars. Unless you were among those who designed them. This observation can easily be refuted by citing some historical references already mentioned and which we will highlight. «In July 1782 the Order of the Illuminati allied itself with Freemasonry during the Congress of Wilhelmsbad, which the historian Freemason Albert Mackey defined as ‘the most important Masonic Congress of the eighteenth century’ – we read on the website Freemasonry Unmasked, full of anecdotes and authoritative historical sources – The participants in that Congress had to swear not to reveal the decisions they had made to anyone (see Nesta H. Webster, World Revolution, 1921, page 31)». Wilhelmsbad Castle was owned by the Ashkenazi Jewish banker (of Khazar-European origins) Mayer Amschel Rothschild who, according to various historians, in 1777 brought together twelve of his most influential friends and convinced them that if they pooled their resources they could dominate the world: this is how the Bavarian Illuminati was born. The French Revolution confirms their success with the annihilation of the first important Catholic Monarchy. It will be the experience of the Paris Commune of 1871, the regurgitation of the regime of terror, that will inspire Lenin in his plan for the subsequent Bolshevik and Communist revolution. So Pike was not only still alive at the time but knew the details. The Independent Order B’nai B’rith or Bené Berith (Hebrew: בני ברית, “sons of the covenant”) is a Jewish lodge founded in 1843 during the presidency of John Tyler and still existing and active. It was founded at the Sinsheimer Café, in the Wall Street neighborhood of New York, by Henry Jones and eleven other people on October 13, 1843. The original name was in German “Bundes-Brueder” (which means “League of Brothers”), in the current one which retains the initials (“BB”). Most of the founders were German-Jews: that is, Ashkenazi like Mayer Amschel Rothschild but also like his descendant Walter Rothschild, eldest son and heir of the banker Nathan Mayer Rothschild, the first Jewish baron of England. Walter Rothschild was among the promoters of the declaration for the formation of the Jewish state in Palestine, later earning the merit of becoming president of the Council of Deputies of British Jews from 1925 to 1926. From these seeds we arrived at 1917 when a letter from the British Foreign Minister Arthur Balfour, addressed to the “Dear Lord Rothschild”, sanctioned Balfour’s declaration which committed the British government to supporting the creation in Palestine of a home for the Jews in respect for the rights of other resident minorities. How did Albert Pike know all these things before they happened? Very simple because he was among those who concerted them in 1860 when the Southern general through Young America planned the American Civil War to defend the right to slavery, Mazzini with Young Italy committed himself to the Expedition of the Thousand and Henry John Temple, 3rd Viscount of Palmerston, British Secretary of State and exponent of the Grand Lodge of England guaranteed all financial and political support. The first expressions of proto-Zionism took shape, for example, in the foundation of the Universal Israelite Alliance in 1860, an organization aimed at the emancipation of the Jewish communities in the Middle East and North Africa, and in the publication of various works, including Rome and Jerusalem, written in 1862 by the German Jewish philosopher Moses Hess, Derishat Zion by the Polish-Prussian rabbi Zvi Hirsch Kalischer, and the hymn Hatikvah, whose lyrics were written by Naftali Herz Imber and which later became the anthem of the State of Israel. Zionism draws its roots from the new cultural environment generated in the context of the emancipation of European Jews starting from the French Revolution and throughout the 19th century and from the Haskalah. The haskalah, with a small delay compared to other Enlightenment movements, arose in Germany and then spread throughout much of Europe and to a small extent also across the Atlantic. The father and inspirer of the movement was Moses Mendelssohn, close to Gotthold Ephraim Lessing, a free thinker of Protestant extraction and an energetic defender of the Jews in Germany. The latter introduced Mendelssohn into the world of Berlin intellectuals where he dedicated himself to the composition of philosophical essays and dissertations. A varied and open movement, the haskalah probably did not close its doors even to exponents of the Frankist heresy, a sort of tail of the messianic movement of Shabatai Zevi which had long been in opposition to official Judaism, perhaps linked to lodges of freemasonry, another force of the times, definitely in relation to the Enlightenment philosophy. Many Jews influenced by the haskalah and the closeness it brought with European culture were seduced by the possibility of assimilation by embracing Christianity. Just think of the family of Karl Marx, descended from rabbis who converted to Protestantism, as did Mendelssohn’s own daughters. Others, however, laid the foundations of the new science of Judaism, the Wissenschaft des Judentums. THE LODGES INSPIRED BY THE SON OF THE BIBLICAL MURDERER CAIN In the previous investigation we highlighted how Marx received the task of writing Capital from British Freemasonry. In other reports we have highlighted the fundamental role played by the Protestants in the birth of the Grand Lodge of London on 24 June 1717. Today we add another detail by recalling the figure of John Theophilus Desaguliers (La Rochelle, 12 March 1683 – Covent Garden, 29 February 1744) who was an English scientist, religious and Freemason of French origins. Desaguliers emigrated to England in 1694, due to the Edict of Fontainebleau, which revoked the freedom of worship of Protestants. He approached Freemasonry, becoming Grand Master of the First Grand Lodge of England in 1718, and Deputy Grand Master in 1723 and 1725. Under his leadership, the Grand Lodge of London and Freemasonry developed in an “astonishing” way in the islands British, to the point that «in 1740 there were already more than 180 lodges». Each of the earliest Masonic texts contains some sort of history of the craft, or guild, of Freemasonry. The oldest work of this type, the Royal Manuscript, dating from 1390 to 1425, has a brief history in the introduction, which states that the “craft of Freemasonry” began with Euclid in Egypt, and arrived in England during the reign of ruler Æðelstan. A little later, the Cooke Manuscript traces Freemasonry to Jabal, son of Lamech (Genesis 4, 20-22), and tells how this knowledge reached Euclid, from him to the children of Israel when they were in Egypt, and so on for an elaborate route to Æðelstan. This myth formed the basis for later manuscript foundations, all of which claim that Freemasonry dates back to Biblical times, and pegs its institutional consolidation in England during the reign of Æðelstan (927-939). Shortly after the formation of the first Grand Lodge of England, James Anderson was commissioned to summarize these “Gothic constitutions” into a pleasing modern form. The constitutions produced by his work have a more widespread historical introduction than any previous one, and once again connect the history of what Freemasonry had become to its biblical roots, always inserting Euclid into the chain of narrative. The first question that a connoisseur of Judeo-Christian history should ask is almost banal. Why do the Freemasons, due to fabulous legendary and historical beliefs, trace Freemasonry to one of the descendants of the murderer Cain and not to the third son of Adam named Set from whom the Semitic culture was born? In this, the manipulation carried out over the centuries by Rabbinic Taldumist Judaism, well described by the Judaism expert Professor Paola Persichetti in the previous investigations in which she highlights the correlations of this Jewish regurgitation following the Destruction of the Temple of Jerusalem, seems evident. In France, Chevalier (Knight) Ramsay’s 1737 conference added Crusader Freemasons to the family tree claiming that they had revived the craft with secrets recovered in the Holy Land, under the patronage of the Knights Hospitaller. At this point, the “history” of the profession of continental Freemasonry separated from that of Freemasonry in England which in the meantime had published its “charter”. THE SCHSM ON THE GREAT ARCHITECT OF THE UNIVERSE The Constitutions of the Free-Masons, “for the use of the lodges” in London and Westminster, was published in 1723. It was edited by the Presbyterian clergyman James Anderson, by order of John Theophilus Desaguliers, and approved by a committee of the grand lodge under its control. The work was reprinted in Philadelphia in 1734 by Benjamin Franklin, who in that year became Grand Master of the Pennsylvania Freemasons. It was also translated into Dutch (1736), German (1741) and French (1745). Anderson was minister of the Presbyterian church in Swallow Street, London, which had formerly been a Huguenot church, and whose pastor in the 1690s was Desaguliers’ father. At the time of his meeting with Desaguliers, he appears to have presented himself as a Talmudic scholar. In various historical testimonies that we summarize for brevity, Anderson himself seems to imply the existence of an Italian Grand Lodge. In Naples in 1728 he saw the light of the first regular Masonic lodge established in Italy, La Perfetta Unione. Raised by the will of the Prince of San Severo, it had Egyptian symbols such as the pyramid, the Sphinx and the radiant sun in its emblem. Subsequently, the English lodge (“La Loggia degli Inglesi”) was established in Florence, founded in 1731 and Freemasonry spread rapidly, despite a series of papal prohibitions. But already ahead the so-called Great Schism occurred. According to a widespread opinion, the schism between French and English Freemasonry originates from the general assembly of the Grand Orient of France in September 1877. Accepting the recommendation contained in a report by the Protestant pastor (and Freemason) Frédéric Desmons, the assembly decided by a majority of amend its constitutions by inserting the formula “its principles are absolute freedom of conscience and human solidarity”. This replaced the previous statement “its principles are the existence of God, the immortality of the soul and human solidarity”. The reaction of the United Grand Lodge of England (UGLE) was the resolution of March 1878 which reiterated “That the Grand Lodge, while anxious to welcome in the most fraternal spirit the Brethren of any foreign Grand Lodge whose proceedings are conducted according to the Ancient cornerstones of the Order, among which the first and most important is the faith in T. G. A. O. T. U. [“the great Architect of the universe”, in English acronym], cannot recognize as ‘true and genuine’ Brothers all those who have been initiated in lodges that deny or ignore that faith.” FREEMASONRY SIMILAR TO THE BEAST OF THE APOCALYPSE Having concluded this long but necessary historical digression on Freemasonry implemented with various Wikipedia sources, let’s return to the beginning. To the book of the Apocalypse of Saint John and the disturbing esoteric symbolisms. If we summarize the historical notes above we can easily conclude that the first promoters of Zionism in the USA were the founders of the B’nai B’rith Lodge composed of Ashkenazi Jews (as Adolph Hitler is also believed to be) that the historians of Jewish culture they define the “13th Tribe of Israel” as they derive from the diaspora of the Khazars who had converted to Judaism for purely political reasons. While in Europe it spread thanks to the Rothschild Dynasty (Red Shield) which was the first to weave subversive plots with an anti-Catholic vocation from the birth of the Bavarian Illuminati up to the pact of terror for the French Revolution from which the liberation of the proto- Zionism together with that Masonic concept of “Liberté, Égalité, Fraternité” imposed by guillotining even the elderly nobles of the Catholic Vendée French region. In light of all this, the words of the Satanist Albert Pike, Pope of American Freemasonry, take on an iconic relevance in the common project between Masonic and Zionist Lodges for the New World Order: «Then everywhere citizens, forced to defend themselves against a world minority of revolutionaries, these destroyers of civilization, and the multitude disillusioned by Christianity, whose worshipers will be devoid of orientation in search of an ideal, will receive the true light through the universal manifestation of pure doctrine of Lucifer finally revealed to the public eye, a manifestation which will be followed by the destruction of Christianity and atheism conquered and crushed at the same time». But following this hermeneutical path to the Book of the Apocalypse, one of the most important allegories comes to mind with disconcerting and terrifying impetus: «The dragon stood on the shore of the sea. And I saw a beast coming out of the sea. It had ten horns and seven heads, with ten crowns on its horns, and on each head a blasphemous name. The beast I saw resembled a leopard, but had feet like those of a bear and a mouth like that of a lion. The dragon gave the beast his power and his throne and great authority. One of the heads of the beast seemed to have had a fatal wound, but the fatal wound had been healed. The whole world was filled with wonder and followed the beast. People worshiped the dragon because he had given authority to the beast, and they also worshiped the beast and asked, “Who is like the beast? Who can wage war against it?» (Rev. 13, 1-4) The prophet Saint John the Apostle and Evangelist delves into the concept with an aura vision «Then I saw a second beast, coming out of the earth. It had two horns like a lamb, but it spoke like a dragon. It exercised all the authority of the first beast on its behalf, and made the earth and its inhabitants worship the first beast, whose fatal wound had been healed» (Rev. 13, 11-12) It is not really scary to note how traditional esoteric Freemasonry became manifest thanks to the Anglican political schism of the Protestants and allowed Pharisaic Judaism, defeated by the Diaspora after the Crucifixion of the Messiah awaited by the Jews, to be reborn in its Talmudic form with Judaism then became with Zionism the most powerful component of the New World Order? We have historical clues that help identify Freemasonry as one of the two apocalyptic Beasts. But this theme will be explored in greater depth if and when we receive from the Holy Spirit the gift of the wisdom necessary to interpret it. Therefore today we cannot help but insinuate doubt… POWER OF CHRIST IN THE PROPHECY OF SAINT JOHN THE APOSTLE But it is precisely Chapter 12 of the Book of the Apocalypse (Rev. 12, 7-12) which comes to illuminate with a radiant dawn of hope the dangers of all of us Christians who strive to be among those “who listen to the words of this prophecy and put into practice the things that are written in it”: «Then war broke out in heaven. Michael and his angels fought against the dragon, and the dragon and his angels fought back. But he was not strong enough, and they lost their place in heaven. The great dragon was hurled down—that ancient serpent called the devil, or Satan, who leads the whole world astray. He was hurled to the earth, and his angels with him». Then I heard a loud voice in heaven say: “Now have come the salvation and the power and the kingdom of our God, and the authority of his Messiah. For the accuser of our brothers and sisters, who accuses them before our God day and night, has been hurled down. They triumphed over him by the blood of the Lamb and by the word of their testimony; they did not love their lives so much as to shrink from death. Therefore rejoice, you heavens and you who dwell in them! But woe to the earth and the sea, because the devil has gone down to you! He is filled with fury, because he knows that his time is short.” Since Saint John was the only Apostle who died without martyrdom for his loyalty to Jesus Christ under the cross and also survived the hell of imprisonment on Patmos (where he received the visions and locutions collected in the Apocalypse), it is probably very useful to start believing him… Subscribe to the Gospa News Newsletter to read the news as soon as it is published Fabio Giuseppe Carlo Carisio © COPYRIGHT GOSPA NEWS prohibition of reproduction without authorization follow Fabio Carisio Gospa News director on Twitter follow Gospa News on Telegram MAIN SOURCES BOOK OF REVELATION (APOCALYPSE) – HOLY BIBLE Epiphanius – Massoneria e sette segrete, Controcorrente Edizioni, pag. 163, 164, 165, 166. – Citazioni da I Nuovi Vespri STORIA DELLA MASSONERIA – WIKIPEDIA GOSPA NEWS – CONSPIRACY – FREEMASONRY – NWO GOSPA NEWS – CHRISTIANS PERSECUTED GOSPA NEWS – WUHAN-GATES DOSSIER GOSPA NEWS – PALESTINE GOSPA NEWS – WAR ZONE GOSPA NEWS – WEAPONS LOBBY DOSSIER GOSPA NEWS – COVID-19, VACCINES & BIG PHARMA DOSSIER Fabio G. C. Carisio Fabio is investigative journalist since 1991. Now geopolitics, intelligence, military, SARS-Cov-2 manmade, NWO expert and Director-founder of Gospa News: a Christian Information Journal. His articles were published on many international media and website as SouthFront, Reseau International, Sputnik Italia, United Nation Association Westminster, Global Research, Kolozeg and more… Most popolar investigation on VT is: Rumsfeld Shady Heritage in Pandemic: GILEAD’s Intrigues with WHO & Wuhan Lab. Bio-Weapons’ Tests with CIA & Pentagon Fabio Giuseppe Carlo Carisio, born on 24/2/1967 in Borgosesia, started working as a reporter when he was only 19 years old in the alpine area of Valsesia, Piedmont, his birth region in Italy. After studying literature and history at the Catholic University of the Sacred Heart in Milan, he became director of the local newspaper Notizia Oggi Vercelli and specialized in judicial reporting. For about 15 years he is a correspondent from Northern Italy for the Italian newspapers Libero and Il Giornale, also writing important revelations on the Ustica massacre, a report on Freemasonry and organized crime. With independent investigations, he collaborates with Carabinieri and Guardia di Finanza in important investigations that conclude with the arrest of Camorra entrepreneurs or corrupt politicians. In July 2018 he found the counter-information web media Gospa News focused on geopolitics, terrorism, Middle East, and military intelligence. In 2020 published the book, in Italian only, WUHAN-GATES – The New World Order Plot on SARS-Cov-2 manmade focused on the cycle of investigations Wuhan-Gates His investigations was quoted also by The Gateway Pundit, Tasnim and others He worked for many years for the magazine Art & Wine as an art critic and curator. VETERANS TODAY OLD POSTS www.gospanews.net/ ATTENTION READERS We See The World From All Sides and Want YOU To Be Fully Informed In fact, intentional disinformation is a disgraceful scourge in media today. So to assuage any possible errant incorrect information posted herein, we strongly encourage you to seek corroboration from other non-VT sources before forming an educated opinion. About VT - Policies & Disclosures - Comment Policy Due to the nature of uncensored content posted by VT's fully independent international writers, VT cannot guarantee absolute validity. All content is owned by the author exclusively. Expressed opinions are NOT necessarily the views of VT, other authors, affiliates, advertisers, sponsors, partners, or technicians. Some content may be satirical in nature. All images are the full responsibility of the article author and NOT VT. https://www.vtforeignpolicy.com/2024/02/freemasonry-zionism-1-apocalyptic-cataclysms-by-synagogue-of-satan/
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    FREEMASONRY & ZIONISM – 1. Apocalyptic “Cataclysms” by Synagogue of Satan
    “To the angel of the church in Smyrna write: These are the words of him who is the First and the Last, who died and came to life again. I know your afflictions and your poverty—yet you are rich! I know about the slander of those who say they are Jews and are not, but are a...
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  • CDC’s Own Scientists Found Masks Ineffective for Covid-19 but Recommended Them Anyway
    Officials at the Centers for Disease Control and Prevention openly questioned the findings of its own scientists’ studies contradicting the agency’s public messaging about mask effectiveness

    World Council for Health
    This article was originally published by The Defender — Children’s Health Defense’s News & Views Website.

    cdc masks ineffective covid feature
    The Centers for Disease Control and Prevention’s (CDC) own scientists conducted studies showing N95 respirators are no more effective at stopping viruses than surgical masks — yet the agency issued guidance contradicting those and other studies showing both types of masks are ineffective at stopping the spread of COVID-19, according to an investigation by independent journalist Paul D. Thacker.

    The investigation, published this week in two parts on The Disinformation Chronicle, details how CDC leadership openly questioned the findings of CDC scientists’ studies contradicting the agency’s public messaging about mask effectiveness.

    During the pandemic, mask advocates “shifted goalposts and demanded N95 respirators,” Thacker said, claiming they perform better than surgical masks at stopping the virus.

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    However, Thacker said CDC scientists found no difference between N95 and surgical masks in the ability to stop the spread of respiratory viruses. The findings of the CDC studies are consistent with other peer-reviewed studies on the efficacy of masks in preventing COVID-19, according to Thacker.

    “But the CDC responded by saying people can’t say that,” Thacker told The Defender.

    To shut down the controversy, the CDC, in its Jan. 23 post on preventing the transmission of pathogens in healthcare settings, warned researchers that to suggest facemasks and respirators are the same “is not scientifically correct,” Thacker wrote.

    CDC ignores own studies questioning N95, mask effectiveness

    According to Thacker, CDC guidance for controlling the spread of infections had not been updated since 2007. This prompted the CDC, in 2022, to select “a bunch of science experts,” and ask them “to update the agency’s scientific guidance to hospitals on how to control infections.”

    In November 2023, the experts produced an 80-page systematic review and meta-analysis, examining whether N95 respirators were more effective than surgical masks. The review found that while N95 respirators are better at filtering particles, the finding that they are more effective at stopping viruses “has been less conclusive.”

    The systematic review also examined the “effectiveness” of N95 respirators and surgical masks “under ‘real world’” conditions and found “no difference” between the two.

    The review also found numerous symptoms reported by N95 mask users, including: “difficulty breathing, headaches, and dizziness; skin barrier damage and itching; fatigue; and difficulty talking.”

    According to Thacker, the CDC is not pleased with these findings, suggesting in its recent update that its own scientists were wrong.

    “Although masks can provide some level of filtration, the level of filtration is not comparable to NIOSH Approved respirators,” the CDC said.

    The post also stated, “The COVID-19 pandemic has forever changed the approach we take in healthcare settings to protect healthcare personnel, patients, and others from transmission of respiratory infections.”

    More evidence contradicting the CDC’s public position came at a June 2023 CDC meeting in Atlanta, when Erin Stone, MPH, a public health analyst in the agency’s Office of Guidelines and Evidence Review, presented the findings of a meta-analysis on the effectiveness of N95 respirators and surgical masks.

    According to Stone, the data “suggests no difference” in their effectiveness.

    Yet, in November 2023 testimony before the U.S. House of Representatives’ Energy and Commerce Committee, CDC Director Mandy Cohen sidestepped questions regarding mask effectiveness and refused to deny she would reinstate mask mandates for children.

    According to Thacker, in December 2023, just six days after Cohen’s testimony, The BMJ’s Archives of Disease in Childhood journal published a study finding that “mask recommendations for children are not supported by scientific evidence.”

    “Recommending child masking does not meet the accepted practice of promulgating only medical interventions where benefits clearly outweigh harms,” the study authors noted.

    Thacker: CDC guidance based on politics, not science

    Thacker said the CDC contradicted its own findings on mask efficacy even in the early stages of the COVID-19 pandemic.

    “Soon after the pandemic started, the CDC began promoting masks to stop the spread of COVID,” Thacker wrote. “And it did so despite CDC publishing a May 2020 policy study in their own journal, ‘Emerging Infectious Diseases,’ that did not find a ‘substantial effect’ for masks in stopping the transmission of respiratory viruses.”


    twitter.com/CDCgov/status/1378462317109731334
    That same month, the CDC began publicly promoting N95 respirators as a more effective means of controlling the spread of COVID-19.

    However, on its webpage promoting the superiority of N95 respirators, the CDC admitted “there’s not a whole lot of evidence that N95 respirators do in fact work better than masks at stopping viruses,” Thacker wrote.

    “Laboratory studies have demonstrated that FFRs [filtering facepiece respirators] provide greater protection against aerosols compared with surgical masks … however, the results of clinical studies have been inconclusive,” the CDC wrote, citing a 2019 study in JAMA comparing N95 respirators to masks.

    “Among outpatient health care personnel, N95 respirators vs medical masks as worn by participants in this trial resulted in no significant difference in the incidence of laboratory-confirmed influenza,” the JAMA study noted.


    twitter.com/CDCgov/status/1256655451195715585
    According to Thacker, the results of these studies confirm the widely accepted pre-COVID-19 scientific consensus on the ineffectiveness of masks of any kind in stopping the spread of viruses. Thacker cited statements the World Health Organization made in 2019 and the CDC’s guidance on virus control.

    In a 2020 appearance on CBS’ “60 Minutes,” Dr. Anthony Fauci said that while a mask might “block a droplet” and “make people feel a little better,” it does not provide “the perfect protection that people think it is.”



    According to Thacker, “For some reason, a ‘masks work’ political movement began to grow,” despite Fauci’s statements and the findings of these studies.

    “I’m not really sure what happened or what we do next,” Thacker wrote. “But something weird took place in America where liberal elites began messaging among themselves ‘masks work.’ They then grew this into a crusade.”

    The movement was effective in getting the CDC on board with issuing mask guidance, Thacker said.

    Four years after the onset of the pandemic, the CDC now openly cheerleads for masks, despite research the agency published showing that masks don’t really protect people from catching viruses, he said.

    “And this is why the experts advising the CDC are getting all this pushback: they didn’t tell the CDC what the CDC wanted to hear,” Thacker wrote.

    Harvey Risch, M.D., Ph.D., professor emeritus and senior research scientist in epidemiology (chronic diseases) at the Yale School of Public Health, told The Disinformation Chronicle the CDC “has succumbed to political influences.”

    Risch said:

    “It made policies for school closures in order to please the teachers’ union. Its charitable organization allows pharma to feed it hundreds of millions of dollars that would be illegal to go directly to the agency, and this gives pharma major influence on CDC policies.”

    According to Thacker, the CDC has continued to double down on guidance promoting mask efficacy. A Jan. 23 letter the agency sent to its own advisers appears to encourage them to add more mask guidance to the agency’s new guidelines for the spread of pathogens, based on the conclusion that N95 respirators are effective.

    “Too much science is forcing CDC to request a science do over,” Thacker wrote, referring to the CDC’s Jan. 23 post, which states that its new recommendations should not “be misread to suggest equivalency between facemasks and NIOSH Approved respirators, which is not scientifically correct nor the intent of the draft language.”

    Thacker said his investigation shows that “in their guidance to the CDC, experts do recommend masks as part of what they call ‘transmission-based guidance’ which the CDC defines as a second tier of infection control.” However, the CDC’s own guidance also finds that masks are effective only for “source control” — preventing an already infected person from infecting others.

    “But this isn’t what the CDC wants,” Thacker wrote. “They want the experts to write guidelines that recommend healthy people wear masks, even though research shows masks won’t really stop healthy people from getting sick.”

    “The CDC has caught the ‘masks work’ political wave and is now demanding that independent experts conform to their preferred mask dictates,” he added.

    In doing so, the CDC is rejecting science it doesn’t like, including several other non-CDC studies that have questioned mask effectiveness.

    A study published in Annals of Internal Medicine in November 2022 found no difference between N95 respirators and surgical masks in stopping the spread of COVID-19. These findings were mirrored in a January 2023 Cochrane meta-analysis on mask effectiveness.

    According to the Cochrane report, “The use of a N95/P2 respirators compared to medical/surgical masks probably makes little or no difference for the objective and more precise outcome of laboratory‐confirmed influenza infection.”

    A May 2023 study published in Ecotoxicology and Environmental Safety suggests N95 respirators may expose wearers to dangerous levels of toxic compounds linked to seizures and cancer.

    A September 2023 meta-analysis published in Clinical Research Study examined mask studies published since 2019 in the CDC’s Morbidity and Mortality Weekly Report (MMWR).

    According to the findings of the meta-analysis:

    “MMWR publications pertaining to masks drew positive conclusions about mask effectiveness >75% of the time despite only 30% testing masks and <15% having statistically significant results. No studies were randomized, yet over half drew causal conclusions.

    “The level of evidence generated was low and the conclusions were most often unsupported by the data. Our findings raise concern about the reliability of the journal for informing health policy.”

    Real-world examples also call into question narratives regarding mask efficacy.

    Sweden, for instance, did not mandate or recommend masks for the general public during the first wave of the COVID-19 pandemic, and only did so in certain situations in the later stages of the pandemic, according to The Conversation. Yet, its total excess deaths during the first two years of the pandemic were among the lowest in Europe.”

    In 2020, Swedish state epidemiologist Anders Tegnell said, “We see no point in wearing a face mask in Sweden, not even on public transport,” adding there were “at least three heavyweight reports … which all state that the scientific evidence is weak.”

    A Swedish government commission noted low levels of excess mortality in 2020 and 2021 and said that, at most, masks should have been “recommended.”

    Soon after the report was released, a Feb. 25, 2022, Boston Herald op-ed stated that Sweden “got it right.”

    “I don’t understand what is driving the ‘masks work’ political movement,” Thacker told The Defender. “There were plenty of stories written pointing out that there isn’t much scientific evidence that masks stop respiratory virus spread.”

    “Maybe people were just scared and wanted to believe masks provide protection?” he said.

    Thacker also cited the historical precedent of the Spanish Flu epidemic in 1918, when the Red Cross campaigned for masks all across America.

    “California’s state board of health ran a study comparing towns that had mask mandates against those that did not. They found that there was no difference and published the study in the American Journal of Public Health in 1920,” Thacker said.

    “Maybe these mask campaigners need to read a little history,” he added.

    Thacker is now calling on whistleblowers inside the CDC to contact him “to discuss what is going on inside the agency.”

    “I’m talking to CDC people and hope to learn what is going on inside the agency. I plan to write more on this,” Thacker told The Defender.

    “CDC Director Mandy Cohen wants to restore trust in the agency, but that won’t happen if she keeps putting politics ahead of scientific evidence,” he said.

    If this content is important to you, share it with your network!

    Share

    This article was written by Michael Nevradakis, Ph.D. and 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.


    If you find value in this Substack and have the means, please consider making a contribution to support the World Council for Health. Thank you.

    Upgrade to Paid Subscription

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    Give Direct to WCH

    https://worldcouncilforhealth.substack.com/p/cdcs-own-scientists-found-masks-ineffective

    https://donshafi911.blogspot.com/2024/02/cdcs-own-scientists-found-masks_16.html
    CDC’s Own Scientists Found Masks Ineffective for Covid-19 but Recommended Them Anyway Officials at the Centers for Disease Control and Prevention openly questioned the findings of its own scientists’ studies contradicting the agency’s public messaging about mask effectiveness World Council for Health This article was originally published by The Defender — Children’s Health Defense’s News & Views Website. cdc masks ineffective covid feature The Centers for Disease Control and Prevention’s (CDC) own scientists conducted studies showing N95 respirators are no more effective at stopping viruses than surgical masks — yet the agency issued guidance contradicting those and other studies showing both types of masks are ineffective at stopping the spread of COVID-19, according to an investigation by independent journalist Paul D. Thacker. The investigation, published this week in two parts on The Disinformation Chronicle, details how CDC leadership openly questioned the findings of CDC scientists’ studies contradicting the agency’s public messaging about mask effectiveness. During the pandemic, mask advocates “shifted goalposts and demanded N95 respirators,” Thacker said, claiming they perform better than surgical masks at stopping the virus. If this content is important to you, share it! Share However, Thacker said CDC scientists found no difference between N95 and surgical masks in the ability to stop the spread of respiratory viruses. The findings of the CDC studies are consistent with other peer-reviewed studies on the efficacy of masks in preventing COVID-19, according to Thacker. “But the CDC responded by saying people can’t say that,” Thacker told The Defender. To shut down the controversy, the CDC, in its Jan. 23 post on preventing the transmission of pathogens in healthcare settings, warned researchers that to suggest facemasks and respirators are the same “is not scientifically correct,” Thacker wrote. CDC ignores own studies questioning N95, mask effectiveness According to Thacker, CDC guidance for controlling the spread of infections had not been updated since 2007. This prompted the CDC, in 2022, to select “a bunch of science experts,” and ask them “to update the agency’s scientific guidance to hospitals on how to control infections.” In November 2023, the experts produced an 80-page systematic review and meta-analysis, examining whether N95 respirators were more effective than surgical masks. The review found that while N95 respirators are better at filtering particles, the finding that they are more effective at stopping viruses “has been less conclusive.” The systematic review also examined the “effectiveness” of N95 respirators and surgical masks “under ‘real world’” conditions and found “no difference” between the two. The review also found numerous symptoms reported by N95 mask users, including: “difficulty breathing, headaches, and dizziness; skin barrier damage and itching; fatigue; and difficulty talking.” According to Thacker, the CDC is not pleased with these findings, suggesting in its recent update that its own scientists were wrong. “Although masks can provide some level of filtration, the level of filtration is not comparable to NIOSH Approved respirators,” the CDC said. The post also stated, “The COVID-19 pandemic has forever changed the approach we take in healthcare settings to protect healthcare personnel, patients, and others from transmission of respiratory infections.” More evidence contradicting the CDC’s public position came at a June 2023 CDC meeting in Atlanta, when Erin Stone, MPH, a public health analyst in the agency’s Office of Guidelines and Evidence Review, presented the findings of a meta-analysis on the effectiveness of N95 respirators and surgical masks. According to Stone, the data “suggests no difference” in their effectiveness. Yet, in November 2023 testimony before the U.S. House of Representatives’ Energy and Commerce Committee, CDC Director Mandy Cohen sidestepped questions regarding mask effectiveness and refused to deny she would reinstate mask mandates for children. According to Thacker, in December 2023, just six days after Cohen’s testimony, The BMJ’s Archives of Disease in Childhood journal published a study finding that “mask recommendations for children are not supported by scientific evidence.” “Recommending child masking does not meet the accepted practice of promulgating only medical interventions where benefits clearly outweigh harms,” the study authors noted. Thacker: CDC guidance based on politics, not science Thacker said the CDC contradicted its own findings on mask efficacy even in the early stages of the COVID-19 pandemic. “Soon after the pandemic started, the CDC began promoting masks to stop the spread of COVID,” Thacker wrote. “And it did so despite CDC publishing a May 2020 policy study in their own journal, ‘Emerging Infectious Diseases,’ that did not find a ‘substantial effect’ for masks in stopping the transmission of respiratory viruses.” twitter.com/CDCgov/status/1378462317109731334 That same month, the CDC began publicly promoting N95 respirators as a more effective means of controlling the spread of COVID-19. However, on its webpage promoting the superiority of N95 respirators, the CDC admitted “there’s not a whole lot of evidence that N95 respirators do in fact work better than masks at stopping viruses,” Thacker wrote. “Laboratory studies have demonstrated that FFRs [filtering facepiece respirators] provide greater protection against aerosols compared with surgical masks … however, the results of clinical studies have been inconclusive,” the CDC wrote, citing a 2019 study in JAMA comparing N95 respirators to masks. “Among outpatient health care personnel, N95 respirators vs medical masks as worn by participants in this trial resulted in no significant difference in the incidence of laboratory-confirmed influenza,” the JAMA study noted. twitter.com/CDCgov/status/1256655451195715585 According to Thacker, the results of these studies confirm the widely accepted pre-COVID-19 scientific consensus on the ineffectiveness of masks of any kind in stopping the spread of viruses. Thacker cited statements the World Health Organization made in 2019 and the CDC’s guidance on virus control. In a 2020 appearance on CBS’ “60 Minutes,” Dr. Anthony Fauci said that while a mask might “block a droplet” and “make people feel a little better,” it does not provide “the perfect protection that people think it is.” According to Thacker, “For some reason, a ‘masks work’ political movement began to grow,” despite Fauci’s statements and the findings of these studies. “I’m not really sure what happened or what we do next,” Thacker wrote. “But something weird took place in America where liberal elites began messaging among themselves ‘masks work.’ They then grew this into a crusade.” The movement was effective in getting the CDC on board with issuing mask guidance, Thacker said. Four years after the onset of the pandemic, the CDC now openly cheerleads for masks, despite research the agency published showing that masks don’t really protect people from catching viruses, he said. “And this is why the experts advising the CDC are getting all this pushback: they didn’t tell the CDC what the CDC wanted to hear,” Thacker wrote. Harvey Risch, M.D., Ph.D., professor emeritus and senior research scientist in epidemiology (chronic diseases) at the Yale School of Public Health, told The Disinformation Chronicle the CDC “has succumbed to political influences.” Risch said: “It made policies for school closures in order to please the teachers’ union. Its charitable organization allows pharma to feed it hundreds of millions of dollars that would be illegal to go directly to the agency, and this gives pharma major influence on CDC policies.” According to Thacker, the CDC has continued to double down on guidance promoting mask efficacy. A Jan. 23 letter the agency sent to its own advisers appears to encourage them to add more mask guidance to the agency’s new guidelines for the spread of pathogens, based on the conclusion that N95 respirators are effective. “Too much science is forcing CDC to request a science do over,” Thacker wrote, referring to the CDC’s Jan. 23 post, which states that its new recommendations should not “be misread to suggest equivalency between facemasks and NIOSH Approved respirators, which is not scientifically correct nor the intent of the draft language.” Thacker said his investigation shows that “in their guidance to the CDC, experts do recommend masks as part of what they call ‘transmission-based guidance’ which the CDC defines as a second tier of infection control.” However, the CDC’s own guidance also finds that masks are effective only for “source control” — preventing an already infected person from infecting others. “But this isn’t what the CDC wants,” Thacker wrote. “They want the experts to write guidelines that recommend healthy people wear masks, even though research shows masks won’t really stop healthy people from getting sick.” “The CDC has caught the ‘masks work’ political wave and is now demanding that independent experts conform to their preferred mask dictates,” he added. In doing so, the CDC is rejecting science it doesn’t like, including several other non-CDC studies that have questioned mask effectiveness. A study published in Annals of Internal Medicine in November 2022 found no difference between N95 respirators and surgical masks in stopping the spread of COVID-19. These findings were mirrored in a January 2023 Cochrane meta-analysis on mask effectiveness. According to the Cochrane report, “The use of a N95/P2 respirators compared to medical/surgical masks probably makes little or no difference for the objective and more precise outcome of laboratory‐confirmed influenza infection.” A May 2023 study published in Ecotoxicology and Environmental Safety suggests N95 respirators may expose wearers to dangerous levels of toxic compounds linked to seizures and cancer. A September 2023 meta-analysis published in Clinical Research Study examined mask studies published since 2019 in the CDC’s Morbidity and Mortality Weekly Report (MMWR). According to the findings of the meta-analysis: “MMWR publications pertaining to masks drew positive conclusions about mask effectiveness >75% of the time despite only 30% testing masks and <15% having statistically significant results. No studies were randomized, yet over half drew causal conclusions. “The level of evidence generated was low and the conclusions were most often unsupported by the data. Our findings raise concern about the reliability of the journal for informing health policy.” Real-world examples also call into question narratives regarding mask efficacy. Sweden, for instance, did not mandate or recommend masks for the general public during the first wave of the COVID-19 pandemic, and only did so in certain situations in the later stages of the pandemic, according to The Conversation. Yet, its total excess deaths during the first two years of the pandemic were among the lowest in Europe.” In 2020, Swedish state epidemiologist Anders Tegnell said, “We see no point in wearing a face mask in Sweden, not even on public transport,” adding there were “at least three heavyweight reports … which all state that the scientific evidence is weak.” A Swedish government commission noted low levels of excess mortality in 2020 and 2021 and said that, at most, masks should have been “recommended.” Soon after the report was released, a Feb. 25, 2022, Boston Herald op-ed stated that Sweden “got it right.” “I don’t understand what is driving the ‘masks work’ political movement,” Thacker told The Defender. “There were plenty of stories written pointing out that there isn’t much scientific evidence that masks stop respiratory virus spread.” “Maybe people were just scared and wanted to believe masks provide protection?” he said. Thacker also cited the historical precedent of the Spanish Flu epidemic in 1918, when the Red Cross campaigned for masks all across America. “California’s state board of health ran a study comparing towns that had mask mandates against those that did not. They found that there was no difference and published the study in the American Journal of Public Health in 1920,” Thacker said. “Maybe these mask campaigners need to read a little history,” he added. Thacker is now calling on whistleblowers inside the CDC to contact him “to discuss what is going on inside the agency.” “I’m talking to CDC people and hope to learn what is going on inside the agency. I plan to write more on this,” Thacker told The Defender. “CDC Director Mandy Cohen wants to restore trust in the agency, but that won’t happen if she keeps putting politics ahead of scientific evidence,” he said. If this content is important to you, share it with your network! Share This article was written by Michael Nevradakis, Ph.D. and 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. If you find value in this Substack and have the means, please consider making a contribution to support the World Council for Health. Thank you. Upgrade to Paid Subscription Refer a friend Donate Subscriptions Give Direct to WCH https://worldcouncilforhealth.substack.com/p/cdcs-own-scientists-found-masks-ineffective https://donshafi911.blogspot.com/2024/02/cdcs-own-scientists-found-masks_16.html
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    CDC’s Own Scientists Found Masks Ineffective for Covid-19 but Recommended Them Anyway
    Officials at the Centers for Disease Control and Prevention openly questioned the findings of its own scientists’ studies contradicting the agency’s public messaging about mask effectiveness
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  • CDC'S own scientists conducted studies showing N95 respirators are no more effective at stopping viruses than surgical masks — yet the agency issued guidance contradicting those and other studies showing both types of masks are ineffective at stopping the spread of COVID-19, according to an investigation by Paul D. Thacker.


    CDC’s Own Scientists Found Masks Ineffective for COVID — But Agency Recommended Them Anyway
    According to an investigation by independent journalist Paul D. Thacker published this week in The Disinformation Chronicle, officials at the Centers for Disease Control and Prevention openly questioned the findings of its own scientists’ studies contradicting the agency’s public messaging about mask effectiveness

    Michael Nevradakis, Ph.D.
    cdc masks ineffective covid feature
    Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free.

    The Centers for Disease Control and Prevention’s (CDC) own scientists conducted studies showing N95 respirators are no more effective at stopping viruses than surgical masks — yet the agency issued guidance contradicting those and other studies showing both types of masks are ineffective at stopping the spread of COVID-19, according to an investigation by independent journalist Paul D. Thacker.

    The investigation, published this week in two parts on The Disinformation Chronicle, details how CDC leadership openly questioned the findings of CDC scientists’ studies contradicting the agency’s public messaging about mask effectiveness.

    During the pandemic, mask advocates “shifted goalposts and demanded N95 respirators,” Thacker said, claiming they perform better than surgical masks at stopping the virus.

    However, Thacker said CDC scientists found no difference between N95 and surgical masks in the ability to stop the spread of respiratory viruses. The findings of the CDC studies are consistent with other peer-reviewed studies on the efficacy of masks in preventing COVID-19, according to Thacker.

    “But the CDC responded by saying people can’t say that,” Thacker told The Defender.

    To shut down the controversy, the CDC, in its Jan. 23 post on preventing the transmission of pathogens in healthcare settings, warned researchers that to suggest facemasks and respirators are the same “is not scientifically correct,” Thacker wrote.

    CDC ignores own studies questioning N95, mask effectiveness

    According to Thacker, CDC guidance for controlling the spread of infections had not been updated since 2007. This prompted the CDC, in 2022, to select “a bunch of science experts,” and ask them “to update the agency’s scientific guidance to hospitals on how to control infections.”

    In November 2023, the experts produced an 80-page systematic review and meta-analysis, examining whether N95 respirators were more effective than surgical masks. The review found that while N95 respirators are better at filtering particles, the finding that they are more effective at stopping viruses “has been less conclusive.”

    The systematic review also examined the “effectiveness” of N95 respirators and surgical masks “under ‘real world’” conditions and found “no difference” between the two.

    The review also found numerous symptoms reported by N95 mask users, including: “difficulty breathing, headaches, and dizziness; skin barrier damage and itching; fatigue; and difficulty talking.”

    According to Thacker, the CDC is not pleased with these findings, suggesting in its recent update that its own scientists were wrong.

    “Although masks can provide some level of filtration, the level of filtration is not comparable to NIOSH Approved respirators,” the CDC said.

    The post also stated, “The COVID-19 pandemic has forever changed the approach we take in healthcare settings to protect healthcare personnel, patients, and others from transmission of respiratory infections.”

    More evidence contradicting the CDC’s public position came at a June 2023 CDC meeting in Atlanta, when Erin Stone, MPH, a public health analyst in the agency’s Office of Guidelines and Evidence Review, presented the findings of a meta-analysis on the effectiveness of N95 respirators and surgical masks.

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    According to Stone, the data “suggests no difference” in their effectiveness.

    Yet, in November 2023 testimony before the U.S. House of Representatives’ Energy and Commerce Committee, CDC Director Mandy Cohen sidestepped questions regarding mask effectiveness and refused to deny she would reinstate mask mandates for children.

    According to Thacker, in December 2023, just six days after Cohen’s testimony, The BMJ’s Archives of Disease in Childhood journal published a study finding that “mask recommendations for children are not supported by scientific evidence.”

    “Recommending child masking does not meet the accepted practice of promulgating only medical interventions where benefits clearly outweigh harms,” the study authors noted.

    Thacker: CDC guidance based on politics, not science

    Thacker said the CDC contradicted its own findings on mask efficacy even in the early stages of the COVID-19 pandemic.

    “Soon after the pandemic started, the CDC began promoting masks to stop the spread of COVID,” Thacker wrote. “And it did so despite CDC publishing a May 2020 policy study in their own journal, ‘Emerging Infectious Diseases,’ that did not find a ‘substantial effect’ for masks in stopping the transmission of respiratory viruses.”


    That same month, the CDC began publicly promoting N95 respirators as a more effective means of controlling the spread of COVID-19.

    However, on its webpage promoting the superiority of N95 respirators, the CDC admitted “there’s not a whole lot of evidence that N95 respirators do in fact work better than masks at stopping viruses,” Thacker wrote.

    “Laboratory studies have demonstrated that FFRs [filtering facepiece respirators] provide greater protection against aerosols compared with surgical masks … however, the results of clinical studies have been inconclusive,” the CDC wrote, citing a 2019 study in JAMA comparing N95 respirators to masks.

    “Among outpatient health care personnel, N95 respirators vs medical masks as worn by participants in this trial resulted in no significant difference in the incidence of laboratory-confirmed influenza,” the JAMA study noted.


    According to Thacker, the results of these studies confirm the widely accepted pre-COVID-19 scientific consensus on the ineffectiveness of masks of any kind in stopping the spread of viruses. Thacker cited statements the World Health Organization made in 2019 and the CDC’s guidance on virus control.

    In a 2020 appearance on CBS’ “60 Minutes,” Dr. Anthony Fauci said that while a mask might “block a droplet” and “make people feel a little better,” it does not provide “the perfect protection that people think it is.”



    According to Thacker, “For some reason, a ‘masks work’ political movement began to grow,” despite Fauci’s statements and the findings of these studies.

    “I’m not really sure what happened or what we do next,” Thacker wrote. “But something weird took place in America where liberal elites began messaging among themselves ‘masks work.’ They then grew this into a crusade.”

    The movement was effective in getting the CDC on board with issuing mask guidance, Thacker said.

    Four years after the onset of the pandemic, the CDC now openly cheerleads for masks, despite research the agency published showing that masks don’t really protect people from catching viruses, he said.

    “And this is why the experts advising the CDC are getting all this pushback: they didn’t tell the CDC what the CDC wanted to hear,” Thacker wrote.

    Harvey Risch, M.D., Ph.D., professor emeritus and senior research scientist in epidemiology (chronic diseases) at the Yale School of Public Health, told The Disinformation Chronicle the CDC “has succumbed to political influences.”

    Risch said:

    “It made policies for school closures in order to please the teachers’ union. Its charitable organization allows pharma to feed it hundreds of millions of dollars that would be illegal to go directly to the agency, and this gives pharma major influence on CDC policies.”

    According to Thacker, the CDC has continued to double down on guidance promoting mask efficacy. A Jan. 23 letter the agency sent to its own advisers appears to encourage them to add more mask guidance to the agency’s new guidelines for the spread of pathogens, based on the conclusion that N95 respirators are effective.

    “Too much science is forcing CDC to request a science do over,” Thacker wrote, referring to the CDC’s Jan. 23 post, which states that its new recommendations should not “be misread to suggest equivalency between facemasks and NIOSH Approved respirators, which is not scientifically correct nor the intent of the draft language.”

    Thacker said his investigation shows that “in their guidance to the CDC, experts do recommend masks as part of what they call ‘transmission-based guidance’ which the CDC defines as a second tier of infection control.” However, the CDC’s own guidance also finds that masks are effective only for “source control” — preventing an already infected person from infecting others.

    “But this isn’t what the CDC wants,” Thacker wrote. “They want the experts to write guidelines that recommend healthy people wear masks, even though research shows masks won’t really stop healthy people from getting sick.”

    “The CDC has caught the ‘masks work’ political wave and is now demanding that independent experts conform to their preferred mask dictates,” he added.

    In doing so, the CDC is rejecting science it doesn’t like, including several other non-CDC studies that have questioned mask effectiveness.

    A study published in Annals of Internal Medicine in November 2022 found no difference between N95 respirators and surgical masks in stopping the spread of COVID-19. These findings were mirrored in a January 2023 Cochrane meta-analysis on mask effectiveness.

    According to the Cochrane report, “The use of a N95/P2 respirators compared to medical/surgical masks probably makes little or no difference for the objective and more precise outcome of laboratory‐confirmed influenza infection.”

    A May 2023 study published in Ecotoxicology and Environmental Safety suggests N95 respirators may expose wearers to dangerous levels of toxic compounds linked to seizures and cancer.

    A September 2023 meta-analysis published in Clinical Research Study examined mask studies published since 2019 in the CDC’s Morbidity and Mortality Weekly Report (MMWR).

    According to the findings of the meta-analysis:

    “MMWR publications pertaining to masks drew positive conclusions about mask effectiveness >75% of the time despite only 30% testing masks and <15% having statistically significant results. No studies were randomized, yet over half drew causal conclusions.

    “The level of evidence generated was low and the conclusions were most often unsupported by the data. Our findings raise concern about the reliability of the journal for informing health policy.”

    Real-world examples also call into question narratives regarding mask efficacy.

    Sweden, for instance, did not mandate or recommend masks for the general public during the first wave of the COVID-19 pandemic, and only did so in certain situations in the later stages of the pandemic, according to The Conversation. Yet, its total excess deaths during the first two years of the pandemic were among the lowest in Europe.”

    In 2020, Swedish state epidemiologist Anders Tegnell said, “We see no point in wearing a face mask in Sweden, not even on public transport,” adding there were “at least three heavyweight reports … which all state that the scientific evidence is weak.”

    A Swedish government commission noted low levels of excess mortality in 2020 and 2021 and said that, at most, masks should have been “recommended.”

    Soon after the report was released, a Feb. 25, 2022, Boston Herald op-ed stated that Sweden “got it right.”

    “I don’t understand what is driving the ‘masks work’ political movement,” Thacker told The Defender. “There were plenty of stories written pointing out that there isn’t much scientific evidence that masks stop respiratory virus spread.”

    “Maybe people were just scared and wanted to believe masks provide protection?” he said.

    Thacker also cited the historical precedent of the Spanish Flu epidemic in 1918, when the Red Cross campaigned for masks all across America.

    “California’s state board of health ran a study comparing towns that had mask mandates against those that did not. They found that there was no difference and published the study in the American Journal of Public Health in 1920,” Thacker said.

    “Maybe these mask campaigners need to read a little history,” he added.

    Thacker is now calling on whistleblowers inside the CDC to contact him “to discuss what is going on inside the agency.”

    “I’m talking to CDC people and hope to learn what is going on inside the agency. I plan to write more on this,” Thacker told The Defender.

    “CDC Director Mandy Cohen wants to restore trust in the agency, but that won’t happen if she keeps putting politics ahead of scientific evidence,” he said.

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    https://childrenshealthdefense.org/defender/cdc-scientists-masks-ineffective-covid-agency-recommended/

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    https://donshafi911.blogspot.com/2024/02/cdcs-own-scientists-found-masks.html
    CDC'S own scientists conducted studies showing N95 respirators are no more effective at stopping viruses than surgical masks — yet the agency issued guidance contradicting those and other studies showing both types of masks are ineffective at stopping the spread of COVID-19, according to an investigation by Paul D. Thacker. CDC’s Own Scientists Found Masks Ineffective for COVID — But Agency Recommended Them Anyway According to an investigation by independent journalist Paul D. Thacker published this week in The Disinformation Chronicle, officials at the Centers for Disease Control and Prevention openly questioned the findings of its own scientists’ studies contradicting the agency’s public messaging about mask effectiveness Michael Nevradakis, Ph.D. cdc masks ineffective covid feature Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. The Centers for Disease Control and Prevention’s (CDC) own scientists conducted studies showing N95 respirators are no more effective at stopping viruses than surgical masks — yet the agency issued guidance contradicting those and other studies showing both types of masks are ineffective at stopping the spread of COVID-19, according to an investigation by independent journalist Paul D. Thacker. The investigation, published this week in two parts on The Disinformation Chronicle, details how CDC leadership openly questioned the findings of CDC scientists’ studies contradicting the agency’s public messaging about mask effectiveness. During the pandemic, mask advocates “shifted goalposts and demanded N95 respirators,” Thacker said, claiming they perform better than surgical masks at stopping the virus. However, Thacker said CDC scientists found no difference between N95 and surgical masks in the ability to stop the spread of respiratory viruses. The findings of the CDC studies are consistent with other peer-reviewed studies on the efficacy of masks in preventing COVID-19, according to Thacker. “But the CDC responded by saying people can’t say that,” Thacker told The Defender. To shut down the controversy, the CDC, in its Jan. 23 post on preventing the transmission of pathogens in healthcare settings, warned researchers that to suggest facemasks and respirators are the same “is not scientifically correct,” Thacker wrote. CDC ignores own studies questioning N95, mask effectiveness According to Thacker, CDC guidance for controlling the spread of infections had not been updated since 2007. This prompted the CDC, in 2022, to select “a bunch of science experts,” and ask them “to update the agency’s scientific guidance to hospitals on how to control infections.” In November 2023, the experts produced an 80-page systematic review and meta-analysis, examining whether N95 respirators were more effective than surgical masks. The review found that while N95 respirators are better at filtering particles, the finding that they are more effective at stopping viruses “has been less conclusive.” The systematic review also examined the “effectiveness” of N95 respirators and surgical masks “under ‘real world’” conditions and found “no difference” between the two. The review also found numerous symptoms reported by N95 mask users, including: “difficulty breathing, headaches, and dizziness; skin barrier damage and itching; fatigue; and difficulty talking.” According to Thacker, the CDC is not pleased with these findings, suggesting in its recent update that its own scientists were wrong. “Although masks can provide some level of filtration, the level of filtration is not comparable to NIOSH Approved respirators,” the CDC said. The post also stated, “The COVID-19 pandemic has forever changed the approach we take in healthcare settings to protect healthcare personnel, patients, and others from transmission of respiratory infections.” More evidence contradicting the CDC’s public position came at a June 2023 CDC meeting in Atlanta, when Erin Stone, MPH, a public health analyst in the agency’s Office of Guidelines and Evidence Review, presented the findings of a meta-analysis on the effectiveness of N95 respirators and surgical masks. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now According to Stone, the data “suggests no difference” in their effectiveness. Yet, in November 2023 testimony before the U.S. House of Representatives’ Energy and Commerce Committee, CDC Director Mandy Cohen sidestepped questions regarding mask effectiveness and refused to deny she would reinstate mask mandates for children. According to Thacker, in December 2023, just six days after Cohen’s testimony, The BMJ’s Archives of Disease in Childhood journal published a study finding that “mask recommendations for children are not supported by scientific evidence.” “Recommending child masking does not meet the accepted practice of promulgating only medical interventions where benefits clearly outweigh harms,” the study authors noted. Thacker: CDC guidance based on politics, not science Thacker said the CDC contradicted its own findings on mask efficacy even in the early stages of the COVID-19 pandemic. “Soon after the pandemic started, the CDC began promoting masks to stop the spread of COVID,” Thacker wrote. “And it did so despite CDC publishing a May 2020 policy study in their own journal, ‘Emerging Infectious Diseases,’ that did not find a ‘substantial effect’ for masks in stopping the transmission of respiratory viruses.” That same month, the CDC began publicly promoting N95 respirators as a more effective means of controlling the spread of COVID-19. However, on its webpage promoting the superiority of N95 respirators, the CDC admitted “there’s not a whole lot of evidence that N95 respirators do in fact work better than masks at stopping viruses,” Thacker wrote. “Laboratory studies have demonstrated that FFRs [filtering facepiece respirators] provide greater protection against aerosols compared with surgical masks … however, the results of clinical studies have been inconclusive,” the CDC wrote, citing a 2019 study in JAMA comparing N95 respirators to masks. “Among outpatient health care personnel, N95 respirators vs medical masks as worn by participants in this trial resulted in no significant difference in the incidence of laboratory-confirmed influenza,” the JAMA study noted. According to Thacker, the results of these studies confirm the widely accepted pre-COVID-19 scientific consensus on the ineffectiveness of masks of any kind in stopping the spread of viruses. Thacker cited statements the World Health Organization made in 2019 and the CDC’s guidance on virus control. In a 2020 appearance on CBS’ “60 Minutes,” Dr. Anthony Fauci said that while a mask might “block a droplet” and “make people feel a little better,” it does not provide “the perfect protection that people think it is.” According to Thacker, “For some reason, a ‘masks work’ political movement began to grow,” despite Fauci’s statements and the findings of these studies. “I’m not really sure what happened or what we do next,” Thacker wrote. “But something weird took place in America where liberal elites began messaging among themselves ‘masks work.’ They then grew this into a crusade.” The movement was effective in getting the CDC on board with issuing mask guidance, Thacker said. Four years after the onset of the pandemic, the CDC now openly cheerleads for masks, despite research the agency published showing that masks don’t really protect people from catching viruses, he said. “And this is why the experts advising the CDC are getting all this pushback: they didn’t tell the CDC what the CDC wanted to hear,” Thacker wrote. Harvey Risch, M.D., Ph.D., professor emeritus and senior research scientist in epidemiology (chronic diseases) at the Yale School of Public Health, told The Disinformation Chronicle the CDC “has succumbed to political influences.” Risch said: “It made policies for school closures in order to please the teachers’ union. Its charitable organization allows pharma to feed it hundreds of millions of dollars that would be illegal to go directly to the agency, and this gives pharma major influence on CDC policies.” According to Thacker, the CDC has continued to double down on guidance promoting mask efficacy. A Jan. 23 letter the agency sent to its own advisers appears to encourage them to add more mask guidance to the agency’s new guidelines for the spread of pathogens, based on the conclusion that N95 respirators are effective. “Too much science is forcing CDC to request a science do over,” Thacker wrote, referring to the CDC’s Jan. 23 post, which states that its new recommendations should not “be misread to suggest equivalency between facemasks and NIOSH Approved respirators, which is not scientifically correct nor the intent of the draft language.” Thacker said his investigation shows that “in their guidance to the CDC, experts do recommend masks as part of what they call ‘transmission-based guidance’ which the CDC defines as a second tier of infection control.” However, the CDC’s own guidance also finds that masks are effective only for “source control” — preventing an already infected person from infecting others. “But this isn’t what the CDC wants,” Thacker wrote. “They want the experts to write guidelines that recommend healthy people wear masks, even though research shows masks won’t really stop healthy people from getting sick.” “The CDC has caught the ‘masks work’ political wave and is now demanding that independent experts conform to their preferred mask dictates,” he added. In doing so, the CDC is rejecting science it doesn’t like, including several other non-CDC studies that have questioned mask effectiveness. A study published in Annals of Internal Medicine in November 2022 found no difference between N95 respirators and surgical masks in stopping the spread of COVID-19. These findings were mirrored in a January 2023 Cochrane meta-analysis on mask effectiveness. According to the Cochrane report, “The use of a N95/P2 respirators compared to medical/surgical masks probably makes little or no difference for the objective and more precise outcome of laboratory‐confirmed influenza infection.” A May 2023 study published in Ecotoxicology and Environmental Safety suggests N95 respirators may expose wearers to dangerous levels of toxic compounds linked to seizures and cancer. A September 2023 meta-analysis published in Clinical Research Study examined mask studies published since 2019 in the CDC’s Morbidity and Mortality Weekly Report (MMWR). According to the findings of the meta-analysis: “MMWR publications pertaining to masks drew positive conclusions about mask effectiveness >75% of the time despite only 30% testing masks and <15% having statistically significant results. No studies were randomized, yet over half drew causal conclusions. “The level of evidence generated was low and the conclusions were most often unsupported by the data. Our findings raise concern about the reliability of the journal for informing health policy.” Real-world examples also call into question narratives regarding mask efficacy. Sweden, for instance, did not mandate or recommend masks for the general public during the first wave of the COVID-19 pandemic, and only did so in certain situations in the later stages of the pandemic, according to The Conversation. Yet, its total excess deaths during the first two years of the pandemic were among the lowest in Europe.” In 2020, Swedish state epidemiologist Anders Tegnell said, “We see no point in wearing a face mask in Sweden, not even on public transport,” adding there were “at least three heavyweight reports … which all state that the scientific evidence is weak.” A Swedish government commission noted low levels of excess mortality in 2020 and 2021 and said that, at most, masks should have been “recommended.” Soon after the report was released, a Feb. 25, 2022, Boston Herald op-ed stated that Sweden “got it right.” “I don’t understand what is driving the ‘masks work’ political movement,” Thacker told The Defender. “There were plenty of stories written pointing out that there isn’t much scientific evidence that masks stop respiratory virus spread.” “Maybe people were just scared and wanted to believe masks provide protection?” he said. Thacker also cited the historical precedent of the Spanish Flu epidemic in 1918, when the Red Cross campaigned for masks all across America. “California’s state board of health ran a study comparing towns that had mask mandates against those that did not. They found that there was no difference and published the study in the American Journal of Public Health in 1920,” Thacker said. “Maybe these mask campaigners need to read a little history,” he added. Thacker is now calling on whistleblowers inside the CDC to contact him “to discuss what is going on inside the agency.” “I’m talking to CDC people and hope to learn what is going on inside the agency. I plan to write more on this,” Thacker told The Defender. “CDC Director Mandy Cohen wants to restore trust in the agency, but that won’t happen if she keeps putting politics ahead of scientific evidence,” he said. DETAILS ⬇️ https://childrenshealthdefense.org/defender/cdc-scientists-masks-ineffective-covid-agency-recommended/ Join ➡️ @ShankaraChetty https://donshafi911.blogspot.com/2024/02/cdcs-own-scientists-found-masks.html
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    CDC’s Own Scientists Found Masks Ineffective for COVID — But Agency Recommended Them Anyway
    According to an investigation by independent journalist Paul D. Thacker published this week in The Disinformation Chronicle, officials at the Centers for Disease Control and Prevention openly questioned the findings of its own scientists’ studies contradicting the agency’s public messaging about mask effectiveness
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  • Staphylococcus aureus bacteria use an immune system trick to colonize up to 80% of humans, and that same strategy to evade vaccine-based immunity.

    This explains why all staph vaccines up to now have failed to provide clinically relevant immunity.

    https://childrenshealthdefense.org/defender/staph-infection-vaccines-fail/

    Join 👉 https://t.me/RogerHodkinson
    Staphylococcus aureus bacteria use an immune system trick to colonize up to 80% of humans, and that same strategy to evade vaccine-based immunity. This explains why all staph vaccines up to now have failed to provide clinically relevant immunity. https://childrenshealthdefense.org/defender/staph-infection-vaccines-fail/ Join 👉 https://t.me/RogerHodkinson
    CHILDRENSHEALTHDEFENSE.ORG
    Why Vaccines for Staph Infections Always Fail
    Staphylococcus aureus bacteria use an immune system trick to colonize up to 80% of humans, and that same strategy to evade vaccine-based immunity. This explains why all staph vaccines up to now have failed to provide clinically relevant immunity, according to a paper published last month in Cell Reports Medicine.
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  • Following the protests in Brussels last week by farmers from across the European Union (EU), the European Commission offered some concessions to the agricultural sector — but said it will not scale back its plan to cut 90% of greenhouse gas emissions by 2040, Reuters reported Tuesday. https://childrenshealthdefense.org/defender/eu-farmers-protest-concession-net-zero-climate/
    Following the protests in Brussels last week by farmers from across the European Union (EU), the European Commission offered some concessions to the agricultural sector — but said it will not scale back its plan to cut 90% of greenhouse gas emissions by 2040, Reuters reported Tuesday. https://childrenshealthdefense.org/defender/eu-farmers-protest-concession-net-zero-climate/
    CHILDRENSHEALTHDEFENSE.ORG
    Protesting Farmers Win Big Concessions, But EU Leaders Dig in Their Heels on Net Zero Climate Target
    After the farmer protests in Brussels last week, European Commission leaders announced concessions to lighten the burden of greenhouse gas reductions on growers, but held the course with plans to cut 90% of emissions by 2040.
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  • ‘Defies Belief’: WHO Does Nothing as Kids’ Chemo Drugs Fail Strength, Purity Tests
    https://childrenshealthdefense.org/defender/who-kids-chemotherapy-drugs-fail-purity-tests-asparaginase/
    ‘Defies Belief’: WHO Does Nothing as Kids’ Chemo Drugs Fail Strength, Purity Tests https://childrenshealthdefense.org/defender/who-kids-chemotherapy-drugs-fail-purity-tests-asparaginase/
    CHILDRENSHEALTHDEFENSE.ORG
    ‘Defies Belief’: WHO Does Nothing as Kids' Chemo Drugs Fail Strength, Purity Tests
    Studies reveal that the chemotherapy medicine asparaginase widely fails purity and strength tests, but a year after warnings, the World Health Organization has failed to take any meaningful action to protect children.
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  • Israel Has Killed Nearly 900 Palestinians Since ICJ Order to Prevent Acts of Genocide
    Buoyed by the staying support of American officials, Israeli forces have continued to commit atrocities in Gaza.

    Prem Thakker February 2 2024, 11:45 a.m.
    30 January 2024, Palestinian Territories, Rafah: Palestinians bury the bodies of 80 Palestinians, who were handed over by the Israeli army through the Kerem Shalom border crossing, in a mass grave. Photo by: Mohammed Talatene/picture-alliance/dpa/AP Images
    In the week since the International Court of Justice ruled that the Israeli government is plausibly committing genocide and ordered it to prevent potential further acts of genocide, Israeli forces have only continued committing atrocities against Palestinians.

    Buoyed by the staying support of American officials, Israeli forces have killed at least 874 Palestinians and injured at least 1,490 in Gaza since last week’s ICJ ruling, according to Palestinian Health Ministry figures from Saturday, January 27, to Friday, February 2. That’s not to mention other acts of Israeli violence in the occupied West Bank and Jerusalem. The loss of life should not be dismissed as “collateral damage,” contrary to what Prime Minister Benjamin Netanyahu has said.

    Video clips and news reports from the past week underscore the ongoing horror. A mass grave with 30 handcuffed, blindfolded, and executed bodies was found in a school in northern Gaza. A 6-year-old girl in Gaza reportedly watched as Israeli forces shot and killed her family inside the very car she was in; she apparently survived, but her whereabouts are now unknown. An Israeli soldier filmed himself in the city of Khan Younis echoing Netanyahu’s rhetoric about the biblical tale of Amalek, where God orders the killing of an entire society — comments that helped South Africa’s lawyers demonstrate Israel’s genocidal intent. “We killed tens of thousands of Amalekites,” the soldier pronounced. “The moral thing is to understand that every Arab is a suspect.”

    During a raid on a refugee camp in occupied Jerusalem, Israeli forces locked a Palestinian person up in chains, forced him into military garb, and used him as a human shield, Al Jazeera reported.

    On Tuesday, Israeli soldiers dressed as medical staff invaded a hospital in the West Bank and executed three Palestinians by shooting them “in the head at point-blank range.” One of them had been in the hospital for nearly four months after being paralyzed by missile fragments from an Israeli drone. Palestinians who were released from an Israeli prison on Thursday shared disturbing testimony of being humiliated inside, their bodies bearing evidence of torture. And in one clip that surfaced this week, an Israeli soldier is seen forcing a busload of kidnapped Palestinians to praise his family and say they will be his family’s slaves.

    Backgrounding the atrocities in Gaza is the broader misery the entire population faces. The BBC noted that UNICEF’s biggest concern is the “estimated 19,000 children who are orphaned or have ended up alone with no adult to look after them.” CNN reported that Palestinians are eating grass and drinking polluted water amid famine conditions. The Guardian reported that 50-62 percent of all buildings in Gaza have likely been damaged or destroyed.

    Earlier this week, a federal court affirmed the ICJ’s finding that Israel may be carrying out a genocide and warned the Biden administration to reconsider its unconditional support for Israel’s war effort. Yet U.S. officials and lawmakers have apparently not gotten the memo.

    The Intercept asked Sen. John Fetterman, D-Pa., to comment on the court rulings that the accusations of genocide by Israel are credible. “I don’t accept that. I reject that. I don’t believe that is Israel’s intention: to commit genocide,” said Fetterman, who has emerged as one of Israel’s most staunch Democratic defenders, on Thursday. “I do believe that their goal is to neutralize or dislodge Hamas from that. And I believe that they certainly do not want to take the lives of any innocent Palestinians and I certainly don’t assign higher value to my children versus a Palestinian child. I mean, I wouldn’t want anybody to die throughout all this tragedy, and it’s just an awful situation.”

    Most Read

    Within hours of the ICJ issuing its ruling last Friday, Israel alleged that 12 of 30,000 — 0.04 percent — employees of the United Nations Relief and Works Agency for Palestine Refugees in the Near East were involved in Hamas’s attack on October 7. The United States immediately suspended its funding of UNRWA, the largest provider of humanitarian aid in Gaza, spurring a cascade of other nations to follow suit.

    Sky News later obtained an Israeli document that actually downgrades the allegation to 0.02 percent of UNRWA staff (six people) being involved in Hamas’s attack. Sky News reported that the documents, which allege further ties between UNRWA and Hamas “make several claims that Sky News has not seen proof of and many of the claims, even if true, do not directly implicate UNRWA.”

    The contrast between the U.S. decision to pause funding based on unverified allegations and its unwillingness to reconsider its military funding of Israel, despite serious allegations of genocide, is stark.

    Fetterman also said that he supports the suspension of funding to UNRWA. When asked why the standard of suspending funding while investigating serious allegations doesn’t apply to the Israeli government, Fetterman dodged the question.

    Fetterman: Well, again, it — well, it’s not. We need a full investigation and find out just how much a part of it was about that and how much, you know, the old question: how much they knew and when they knew that.

    The Intercept: So you’re saying that for Israel as well?

    Fetterman: Yeah, OK, so good, all right, well good.

    Reporter Said Arikat confronted State Department spokesperson Matthew Miller on the tension Wednesday. “I’ll say with respect to the charges of genocide, we believe that they’re unfounded,” Miller said. “We continue to support Israel’s right to take action to ensure that the terrorist attacks of October 7th cannot be repeated, but we want them to do so in a way that complies with — fully with international humanitarian law.”

    Miller was then asked about Israel receiving aid even as Israeli government officials call for the ethnic cleansing of Palestinians and maintain good standing in government.

    “When the secretary traveled to Israel on his most recent visit,” Miller said, “he made clear that he thought it was important that the Israeli government speak out against those matters and those comments publicly and reiterate that it is not the policy of the Israeli government to force Palestinians from Gaza.”

    But, as has continued to be the case, Israeli officials have stepped on the assurances of the U.S. Two days after the ICJ ordered the Israeli government to prevent and punish incitements of genocide from public officials, National Security Minister Itamar Ben-Gvir and Finance Minister Bezalel Smotrich were among 11 cabinet ministers and 15 coalition members of the Knesset who rallied at conference hosted by hundreds of settlers calling for the settlement of Gaza.

    On Tuesday, Defense Minister Yoav Gallant reportedly told members of the Knesset’s Foreign Affairs and Defense Committee that afte​​r their military campaign ends, Israel will maintain military control of Gaza, so it can operate similarly to the way it does in the West Bank.

    On Thursday, Smotrich said that allowing aid into Gaza contradicts the goals of Israel’s campaign, and that he spoke with Netanyahu, who supposedly assured him that things will change soon. Israeli ministers Benny Gantz and Gadi Eisenkot reportedly called to limit humanitarian aid as well. Meanwhile, at aid crossings, people in Israel have taken cue from their leaders, attempting to block aid trucks from entering Gaza, where hundreds of thousands of people — including the hostages held by Hamas — are at risk of starvation and malnutrition, every day since the ICJ ruling.

    One clip even shows a right-wing activist telling an aid truck driver, a Palestinian citizen of Israel, that “I am the owner here, you are a slave here.”

    https://theintercept.com/2024/02/02/israel-gaza-icj-palestinian-deaths/

    https://donshafi911.blogspot.com/2024/02/israel-has-killed-nearly-900.html
    Israel Has Killed Nearly 900 Palestinians Since ICJ Order to Prevent Acts of Genocide Buoyed by the staying support of American officials, Israeli forces have continued to commit atrocities in Gaza. Prem Thakker February 2 2024, 11:45 a.m. 30 January 2024, Palestinian Territories, Rafah: Palestinians bury the bodies of 80 Palestinians, who were handed over by the Israeli army through the Kerem Shalom border crossing, in a mass grave. Photo by: Mohammed Talatene/picture-alliance/dpa/AP Images In the week since the International Court of Justice ruled that the Israeli government is plausibly committing genocide and ordered it to prevent potential further acts of genocide, Israeli forces have only continued committing atrocities against Palestinians. Buoyed by the staying support of American officials, Israeli forces have killed at least 874 Palestinians and injured at least 1,490 in Gaza since last week’s ICJ ruling, according to Palestinian Health Ministry figures from Saturday, January 27, to Friday, February 2. That’s not to mention other acts of Israeli violence in the occupied West Bank and Jerusalem. The loss of life should not be dismissed as “collateral damage,” contrary to what Prime Minister Benjamin Netanyahu has said. Video clips and news reports from the past week underscore the ongoing horror. A mass grave with 30 handcuffed, blindfolded, and executed bodies was found in a school in northern Gaza. A 6-year-old girl in Gaza reportedly watched as Israeli forces shot and killed her family inside the very car she was in; she apparently survived, but her whereabouts are now unknown. An Israeli soldier filmed himself in the city of Khan Younis echoing Netanyahu’s rhetoric about the biblical tale of Amalek, where God orders the killing of an entire society — comments that helped South Africa’s lawyers demonstrate Israel’s genocidal intent. “We killed tens of thousands of Amalekites,” the soldier pronounced. “The moral thing is to understand that every Arab is a suspect.” During a raid on a refugee camp in occupied Jerusalem, Israeli forces locked a Palestinian person up in chains, forced him into military garb, and used him as a human shield, Al Jazeera reported. On Tuesday, Israeli soldiers dressed as medical staff invaded a hospital in the West Bank and executed three Palestinians by shooting them “in the head at point-blank range.” One of them had been in the hospital for nearly four months after being paralyzed by missile fragments from an Israeli drone. Palestinians who were released from an Israeli prison on Thursday shared disturbing testimony of being humiliated inside, their bodies bearing evidence of torture. And in one clip that surfaced this week, an Israeli soldier is seen forcing a busload of kidnapped Palestinians to praise his family and say they will be his family’s slaves. Backgrounding the atrocities in Gaza is the broader misery the entire population faces. The BBC noted that UNICEF’s biggest concern is the “estimated 19,000 children who are orphaned or have ended up alone with no adult to look after them.” CNN reported that Palestinians are eating grass and drinking polluted water amid famine conditions. The Guardian reported that 50-62 percent of all buildings in Gaza have likely been damaged or destroyed. Earlier this week, a federal court affirmed the ICJ’s finding that Israel may be carrying out a genocide and warned the Biden administration to reconsider its unconditional support for Israel’s war effort. Yet U.S. officials and lawmakers have apparently not gotten the memo. The Intercept asked Sen. John Fetterman, D-Pa., to comment on the court rulings that the accusations of genocide by Israel are credible. “I don’t accept that. I reject that. I don’t believe that is Israel’s intention: to commit genocide,” said Fetterman, who has emerged as one of Israel’s most staunch Democratic defenders, on Thursday. “I do believe that their goal is to neutralize or dislodge Hamas from that. And I believe that they certainly do not want to take the lives of any innocent Palestinians and I certainly don’t assign higher value to my children versus a Palestinian child. I mean, I wouldn’t want anybody to die throughout all this tragedy, and it’s just an awful situation.” Most Read Within hours of the ICJ issuing its ruling last Friday, Israel alleged that 12 of 30,000 — 0.04 percent — employees of the United Nations Relief and Works Agency for Palestine Refugees in the Near East were involved in Hamas’s attack on October 7. The United States immediately suspended its funding of UNRWA, the largest provider of humanitarian aid in Gaza, spurring a cascade of other nations to follow suit. Sky News later obtained an Israeli document that actually downgrades the allegation to 0.02 percent of UNRWA staff (six people) being involved in Hamas’s attack. Sky News reported that the documents, which allege further ties between UNRWA and Hamas “make several claims that Sky News has not seen proof of and many of the claims, even if true, do not directly implicate UNRWA.” The contrast between the U.S. decision to pause funding based on unverified allegations and its unwillingness to reconsider its military funding of Israel, despite serious allegations of genocide, is stark. Fetterman also said that he supports the suspension of funding to UNRWA. When asked why the standard of suspending funding while investigating serious allegations doesn’t apply to the Israeli government, Fetterman dodged the question. Fetterman: Well, again, it — well, it’s not. We need a full investigation and find out just how much a part of it was about that and how much, you know, the old question: how much they knew and when they knew that. The Intercept: So you’re saying that for Israel as well? Fetterman: Yeah, OK, so good, all right, well good. Reporter Said Arikat confronted State Department spokesperson Matthew Miller on the tension Wednesday. “I’ll say with respect to the charges of genocide, we believe that they’re unfounded,” Miller said. “We continue to support Israel’s right to take action to ensure that the terrorist attacks of October 7th cannot be repeated, but we want them to do so in a way that complies with — fully with international humanitarian law.” Miller was then asked about Israel receiving aid even as Israeli government officials call for the ethnic cleansing of Palestinians and maintain good standing in government. “When the secretary traveled to Israel on his most recent visit,” Miller said, “he made clear that he thought it was important that the Israeli government speak out against those matters and those comments publicly and reiterate that it is not the policy of the Israeli government to force Palestinians from Gaza.” But, as has continued to be the case, Israeli officials have stepped on the assurances of the U.S. Two days after the ICJ ordered the Israeli government to prevent and punish incitements of genocide from public officials, National Security Minister Itamar Ben-Gvir and Finance Minister Bezalel Smotrich were among 11 cabinet ministers and 15 coalition members of the Knesset who rallied at conference hosted by hundreds of settlers calling for the settlement of Gaza. On Tuesday, Defense Minister Yoav Gallant reportedly told members of the Knesset’s Foreign Affairs and Defense Committee that afte​​r their military campaign ends, Israel will maintain military control of Gaza, so it can operate similarly to the way it does in the West Bank. On Thursday, Smotrich said that allowing aid into Gaza contradicts the goals of Israel’s campaign, and that he spoke with Netanyahu, who supposedly assured him that things will change soon. Israeli ministers Benny Gantz and Gadi Eisenkot reportedly called to limit humanitarian aid as well. Meanwhile, at aid crossings, people in Israel have taken cue from their leaders, attempting to block aid trucks from entering Gaza, where hundreds of thousands of people — including the hostages held by Hamas — are at risk of starvation and malnutrition, every day since the ICJ ruling. One clip even shows a right-wing activist telling an aid truck driver, a Palestinian citizen of Israel, that “I am the owner here, you are a slave here.” https://theintercept.com/2024/02/02/israel-gaza-icj-palestinian-deaths/ https://donshafi911.blogspot.com/2024/02/israel-has-killed-nearly-900.html
    THEINTERCEPT.COM
    Israel Has Killed Nearly 900 Palestinians Since ICJ Order to Prevent Acts of Genocide
    Buoyed by the staying support of American officials, Israeli forces have continued to commit atrocities in Gaza.
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  • The Truth About HPV Vaccination, Part 3: Can It Prevent Cervical Cancer?
    There are no valid studies showing the vaccine for the human papillomavirus, or HPV, prevents cervical cancer. However, there are studies suggesting the vaccine could increase the risk of cancer.

    The Epoch Times

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    By Dr. Yuhong Dong

    Editor’s Note: This third installment in a multi-part series about the human papillomavirus, or HPV, vaccine examines studies that link the vaccines to increased risk of serious neurological and autoimmune disorders. Read Part 1 here and Part 2 here.

    In part 1 and part 2 of this series, we discussed the human papillomavirus (HPV) vaccine and its links to ovarian insufficiency and autoimmune disease.

    In part 3, we turn to questions regarding the effectiveness of the vaccine to prevent cervical cancer, and the limitations of relevant clinical trials to detect such a type of effect.

    Summary of key facts

    There are multiple obstacles in designing a valid clinical trial to prove the HPV vaccine could prevent cervical cancer, e.g. long lead time, lack of adequate informed consent, complexity between HPV infection and cervical cancer and the negative impact of girls’ sexual behavior, which may worsen the risks of cervical cancer.
    Most of the HPV’s interventional clinical trials have too short a follow-up time to draw a concrete conclusion.
    In a large Swedish observational trial, which is treated as the most convincing study to prove the HPV vaccine’s effects on cervical cancer, a few confounding factors were not adequately balanced between the HPV vaccination group versus the unvaccinated group.
    The National Cancer Institute’s Surveillance, Epidemiology, and End Results Program (SEER) data and another U.S. study found the HPV vaccine has no effects in reducing cancer rates.
    Two other registry-based studies in Australia and the U.K. suggest that HPV vaccination is associated with increased cervical cancer rates in certain age groups.
    Long lead time from HPV infection to cervical cancer

    Typically, there is a long period from HPV infection to cervical epithelium abnormalities, then cervical cancer.

    HPV infections usually last 12–18 months and are eventually cleared by the immune system.

    Fewer than 10% of HPV infections are persistent.

    There are two types of precancerous cervical lesions, low-grade or high-grade. Low-grade cervical neoplasia grade 1 (CIN1) is usually transient and resolves naturally within one to two years.

    Only a few persistent infections progress to the clinically meaningful high-grade, CIN2 or 3. Meanwhile, the median time from CIN2/3 to transition to cancer is estimated to be 23.5 years.

    Among those with weakened immune systems, HPV-related cancer might progress more quickly.

    In a review of the natural history of HPV infection, the complex pathway from infection to cancer is elucidated, including what is known (purple boxes) and where uncertainty remains (blue boxes).



    Difficulty running clinical trials for the HPV vaccine

    Because of the long lead time from HPV infection to cervical cancer, a prospective, randomized controlled trial is not easily designed and feasibly implemented.

    Lack of long-term follow-up is a common issue for most clinical trials to prove the HPV vaccine’s effectiveness in preventing cervical cancer.

    For example, a 2007 study found that Gardasil was effective in reducing HPV-associated cervical precancerous lesions rate by 20%.

    This study followed their subjects for only an average of three years after administration of the first dose.

    Furthermore, due to the complex uncertainties in the natural history between HPV infection and cervical cancer, it is not easy to claim the effectiveness of the HPV vaccine.

    A randomized trial is designed to balance the two groups — vaccine and placebo — so that any unmeasured confounding variables which might influence the outcome of the trial are distributed evenly.

    However, if the treatment group knows they got the vaccine, might their behaviors change? Might they be less risk-averse, thinking they have some protection?

    For example, girls might think they are vaccinated and “protected” from cervical cancer and may tend to initiate sexual intercourse at a younger age or engage in sexual activities with more partners.

    However, sexual intercourse at a young age, multiple sexual partners and oral contraceptive use are associated with an increased risk of cervical cancer in women.

    In other words, HPV vaccination may offer some protection if offered before sexual activity is initiated, but it may also be associated with increased behavioral risk factors.

    Whether the benefits of vaccination outweigh any risks is therefore a multifactorial question deserving of careful longitudinal study.

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    Systemic analysis of 12 clinical trials on HPV vaccine efficacy

    In 2020, a Queen Mary University study led by Dr. Claire Rees reviewed 12 randomized clinical trials for Cervarix and Gardasil. The investigators found that the trials did not include populations representative of the vaccination target groups, and the trial design may have overstated vaccine efficacy.

    For example, one trial design generated evidence that the vaccine prevents CIN1. But this is not meaningful because these lesions usually resolve on their own.

    Furthermore, the study accessed efficacy against low-grade precancerous lesions. But this is not necessarily suggestive of efficacy against the more serious but much less frequent high-grade lesions.

    Finally, the cytology screenings were done every six to 12 months instead of every 36 months (normal screening interval), meaning the efficacy of the vaccine may have been overestimated, as low-grade lesions could go away spontaneously.

    All this is to say the HPV vaccine may be effective at preventing more serious lesions which lead to cervical cancer, but it is hard to know because of these poorly designed trials.

    Nothing is conclusive without a larger trial powered to detect a difference in rates of more serious cervical changes according to the typical screening schedule. However, such a trial has not yet been performed.

    Swedish nationwide health registry study

    A nationwide Swedish health registry-based study followed 1,672,983 women for 12 years to assess the association between HPV vaccination and the risk of cervical cancer.

    In this study, the cumulative incidence of cervical cancer was 47 cases per 100,000 women vaccinated and 94 per 100,000 unvaccinated, suggesting that HPV4 vaccination was associated with a reduced risk of 49 to 63% of invasive cervical cancer at the population level.

    Even though the results are positive, the study researchers raised a few concerns themselves.

    First, HPV-vaccinated women could have been generally healthier than unvaccinated women. This is known as “healthy volunteer bias.”

    Second, a mother’s history of cervical cancer might be associated with both vaccination uptake and underlying risk of cervical cancer as well as screening rates.

    Third, lifestyle and health factors such as smoking, sexual intercourse at a young age, multiple sexual partners, oral contraceptive use and obesity are reportedly associated with the risk of cervical cancer.

    These factors have not been thoroughly analyzed by this study and could have contributed to the data.

    Furthermore, parental education level and annual household income level may be interconnected with lifestyle factors such as smoking status.

    Strengths of this study include its size, duration and outcome of interest being invasive cancer, not low-grade lesions. However, it is impossible to exclude the relationship between lifestyle factors, vaccination uptake and cervical cancer.

    Only a randomized controlled trial (RCT) could balance the two groups on these unmeasured — but related — risk factors.

    However even if the risk factors (sexual behaviors) are fully balanced at baseline with an RCT, it is hard to keep them still balanced during the whole study course after HPV vaccination.

    No association found in a U.S. database

    Meanwhile, researchers found no association between vaccination and cancer mortality in the U.S.

    According to the National Cancer Institute’s SEER program, the incidence of deaths from cervical cancer before Gardasil’s introduction in the U.S. had been steadily declining for years and, in 2006, was 2.4 per 100,000 women.

    The data from 2016–2020 is 2.2 per 100,000 women — essentially unchanged.

    In a cross-sectional study using a nationally representative sample of U.S. adults aged 20–59 years, among 9,891 participants, the researchers did not find an association between HPV vaccination and HPV-related cancers.

    Increase in cervical cancer after HPV vaccine rollout: Australia

    In Australia, government data similarly reveal an increase in cervical cancer rates in certain age groups of women following the implementation of the Gardasil vaccine.

    Thirteen years after Gardasil was recommended for teenagers and young adults, there has been a 30% increase in 30- to 34-year-old women (4.9 cases/100,000 compared to 6.6 cases/100,000 in 2020) being diagnosed with cervical cancer.

    Even though the rates decreased in other age groups, the abnormal increase in the 30–34 age group needs an explanation.



    Several factors should be considered.

    First, this database does not tell the stage of cancer. More cancer diagnosed at an early stage may result in a cancer-rate increase.

    Second, decreasing cancer rates could be caused by declines in screening rates, perhaps due to the pandemic and/or a reluctance to get tested.

    Third, Australia has an increasing proportion of immigrants from South Asia, and these cultural factors may influence the cervical cancer-screening rate.

    A study of South Asian women living in Australia found that almost half had never had a previous screening test.

    Cervical cancer rates rise after HPV vaccination in the UK

    In the U.K., HPV vaccination was introduced in 2008 for girls aged 12–13 with catch-up for those aged 14–18. Many expected cervical cancer rates in women aged 20–24 to fall by 2014 as the vaccinated cohorts entered their 20s.

    However, in 2016 national statistics showed a worrying and substantial 70% increase in the rate of cervical cancer at ages 20 to 24 (i.e. from 2.7 in 2012 to 4.6 per 100,000 in 2014).

    While the author would consider it to be too early to draw conclusions regarding vaccine efficacy in protecting against cancer, this merits further study.

    Accordingly, an analysis was conducted in the U.K. in 2018 in response to public interest regarding this increase in cervical cancer.

    Researchers from Queen Mary University and King’s College London found that it was attributable to an increase in the proportion of women first screened at age 24.5 years.

    The increase was limited to stage I cervical cancer. But there was no evidence of a lack of screening leading to increasing rates.

    While the researchers considered it too early to conclude vaccine efficacy in protecting against cancer, these findings merit further study.

    Could HPV vaccines make HPV infections worse?

    Besides the vaccine’s unclear effectiveness in cancer prevention, studies further suggest the suppression of the HPV strains targeted by the vaccine may induce more virulent strains.

    For example, a 2015 study found that vaccinated young adult women had a higher prevalence of high-risk HPV types other than types 16 and 18, putting them at risk for more aggressive cervical and other HPV-related cancers.

    Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases in China, is the chief scientific officer and co-founder of a Swiss biotech company and former senior medical scientific expert for antiviral drug development at Novartis Pharma in Switzerland.

    If you or your child suffered harm after receiving the Gardasil HPV vaccine, you may have a legal claim. Please visit Wisner Baum for a free case evaluation. Click here to watch a Gardasil litigation update interview with Wisner Baum Senior Partner Bijan Esfandiari.

    https://childrenshealthdefense.org/defender/truth-hpv-vaccine-part-3-et/


    https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-3.html
    The Truth About HPV Vaccination, Part 3: Can It Prevent Cervical Cancer? There are no valid studies showing the vaccine for the human papillomavirus, or HPV, prevents cervical cancer. However, there are studies suggesting the vaccine could increase the risk of cancer. The Epoch Times Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. By Dr. Yuhong Dong Editor’s Note: This third installment in a multi-part series about the human papillomavirus, or HPV, vaccine examines studies that link the vaccines to increased risk of serious neurological and autoimmune disorders. Read Part 1 here and Part 2 here. In part 1 and part 2 of this series, we discussed the human papillomavirus (HPV) vaccine and its links to ovarian insufficiency and autoimmune disease. In part 3, we turn to questions regarding the effectiveness of the vaccine to prevent cervical cancer, and the limitations of relevant clinical trials to detect such a type of effect. Summary of key facts There are multiple obstacles in designing a valid clinical trial to prove the HPV vaccine could prevent cervical cancer, e.g. long lead time, lack of adequate informed consent, complexity between HPV infection and cervical cancer and the negative impact of girls’ sexual behavior, which may worsen the risks of cervical cancer. Most of the HPV’s interventional clinical trials have too short a follow-up time to draw a concrete conclusion. In a large Swedish observational trial, which is treated as the most convincing study to prove the HPV vaccine’s effects on cervical cancer, a few confounding factors were not adequately balanced between the HPV vaccination group versus the unvaccinated group. The National Cancer Institute’s Surveillance, Epidemiology, and End Results Program (SEER) data and another U.S. study found the HPV vaccine has no effects in reducing cancer rates. Two other registry-based studies in Australia and the U.K. suggest that HPV vaccination is associated with increased cervical cancer rates in certain age groups. Long lead time from HPV infection to cervical cancer Typically, there is a long period from HPV infection to cervical epithelium abnormalities, then cervical cancer. HPV infections usually last 12–18 months and are eventually cleared by the immune system. Fewer than 10% of HPV infections are persistent. There are two types of precancerous cervical lesions, low-grade or high-grade. Low-grade cervical neoplasia grade 1 (CIN1) is usually transient and resolves naturally within one to two years. Only a few persistent infections progress to the clinically meaningful high-grade, CIN2 or 3. Meanwhile, the median time from CIN2/3 to transition to cancer is estimated to be 23.5 years. Among those with weakened immune systems, HPV-related cancer might progress more quickly. In a review of the natural history of HPV infection, the complex pathway from infection to cancer is elucidated, including what is known (purple boxes) and where uncertainty remains (blue boxes). Difficulty running clinical trials for the HPV vaccine Because of the long lead time from HPV infection to cervical cancer, a prospective, randomized controlled trial is not easily designed and feasibly implemented. Lack of long-term follow-up is a common issue for most clinical trials to prove the HPV vaccine’s effectiveness in preventing cervical cancer. For example, a 2007 study found that Gardasil was effective in reducing HPV-associated cervical precancerous lesions rate by 20%. This study followed their subjects for only an average of three years after administration of the first dose. Furthermore, due to the complex uncertainties in the natural history between HPV infection and cervical cancer, it is not easy to claim the effectiveness of the HPV vaccine. A randomized trial is designed to balance the two groups — vaccine and placebo — so that any unmeasured confounding variables which might influence the outcome of the trial are distributed evenly. However, if the treatment group knows they got the vaccine, might their behaviors change? Might they be less risk-averse, thinking they have some protection? For example, girls might think they are vaccinated and “protected” from cervical cancer and may tend to initiate sexual intercourse at a younger age or engage in sexual activities with more partners. However, sexual intercourse at a young age, multiple sexual partners and oral contraceptive use are associated with an increased risk of cervical cancer in women. In other words, HPV vaccination may offer some protection if offered before sexual activity is initiated, but it may also be associated with increased behavioral risk factors. Whether the benefits of vaccination outweigh any risks is therefore a multifactorial question deserving of careful longitudinal study. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now Systemic analysis of 12 clinical trials on HPV vaccine efficacy In 2020, a Queen Mary University study led by Dr. Claire Rees reviewed 12 randomized clinical trials for Cervarix and Gardasil. The investigators found that the trials did not include populations representative of the vaccination target groups, and the trial design may have overstated vaccine efficacy. For example, one trial design generated evidence that the vaccine prevents CIN1. But this is not meaningful because these lesions usually resolve on their own. Furthermore, the study accessed efficacy against low-grade precancerous lesions. But this is not necessarily suggestive of efficacy against the more serious but much less frequent high-grade lesions. Finally, the cytology screenings were done every six to 12 months instead of every 36 months (normal screening interval), meaning the efficacy of the vaccine may have been overestimated, as low-grade lesions could go away spontaneously. All this is to say the HPV vaccine may be effective at preventing more serious lesions which lead to cervical cancer, but it is hard to know because of these poorly designed trials. Nothing is conclusive without a larger trial powered to detect a difference in rates of more serious cervical changes according to the typical screening schedule. However, such a trial has not yet been performed. Swedish nationwide health registry study A nationwide Swedish health registry-based study followed 1,672,983 women for 12 years to assess the association between HPV vaccination and the risk of cervical cancer. In this study, the cumulative incidence of cervical cancer was 47 cases per 100,000 women vaccinated and 94 per 100,000 unvaccinated, suggesting that HPV4 vaccination was associated with a reduced risk of 49 to 63% of invasive cervical cancer at the population level. Even though the results are positive, the study researchers raised a few concerns themselves. First, HPV-vaccinated women could have been generally healthier than unvaccinated women. This is known as “healthy volunteer bias.” Second, a mother’s history of cervical cancer might be associated with both vaccination uptake and underlying risk of cervical cancer as well as screening rates. Third, lifestyle and health factors such as smoking, sexual intercourse at a young age, multiple sexual partners, oral contraceptive use and obesity are reportedly associated with the risk of cervical cancer. These factors have not been thoroughly analyzed by this study and could have contributed to the data. Furthermore, parental education level and annual household income level may be interconnected with lifestyle factors such as smoking status. Strengths of this study include its size, duration and outcome of interest being invasive cancer, not low-grade lesions. However, it is impossible to exclude the relationship between lifestyle factors, vaccination uptake and cervical cancer. Only a randomized controlled trial (RCT) could balance the two groups on these unmeasured — but related — risk factors. However even if the risk factors (sexual behaviors) are fully balanced at baseline with an RCT, it is hard to keep them still balanced during the whole study course after HPV vaccination. No association found in a U.S. database Meanwhile, researchers found no association between vaccination and cancer mortality in the U.S. According to the National Cancer Institute’s SEER program, the incidence of deaths from cervical cancer before Gardasil’s introduction in the U.S. had been steadily declining for years and, in 2006, was 2.4 per 100,000 women. The data from 2016–2020 is 2.2 per 100,000 women — essentially unchanged. In a cross-sectional study using a nationally representative sample of U.S. adults aged 20–59 years, among 9,891 participants, the researchers did not find an association between HPV vaccination and HPV-related cancers. Increase in cervical cancer after HPV vaccine rollout: Australia In Australia, government data similarly reveal an increase in cervical cancer rates in certain age groups of women following the implementation of the Gardasil vaccine. Thirteen years after Gardasil was recommended for teenagers and young adults, there has been a 30% increase in 30- to 34-year-old women (4.9 cases/100,000 compared to 6.6 cases/100,000 in 2020) being diagnosed with cervical cancer. Even though the rates decreased in other age groups, the abnormal increase in the 30–34 age group needs an explanation. Several factors should be considered. First, this database does not tell the stage of cancer. More cancer diagnosed at an early stage may result in a cancer-rate increase. Second, decreasing cancer rates could be caused by declines in screening rates, perhaps due to the pandemic and/or a reluctance to get tested. Third, Australia has an increasing proportion of immigrants from South Asia, and these cultural factors may influence the cervical cancer-screening rate. A study of South Asian women living in Australia found that almost half had never had a previous screening test. Cervical cancer rates rise after HPV vaccination in the UK In the U.K., HPV vaccination was introduced in 2008 for girls aged 12–13 with catch-up for those aged 14–18. Many expected cervical cancer rates in women aged 20–24 to fall by 2014 as the vaccinated cohorts entered their 20s. However, in 2016 national statistics showed a worrying and substantial 70% increase in the rate of cervical cancer at ages 20 to 24 (i.e. from 2.7 in 2012 to 4.6 per 100,000 in 2014). While the author would consider it to be too early to draw conclusions regarding vaccine efficacy in protecting against cancer, this merits further study. Accordingly, an analysis was conducted in the U.K. in 2018 in response to public interest regarding this increase in cervical cancer. Researchers from Queen Mary University and King’s College London found that it was attributable to an increase in the proportion of women first screened at age 24.5 years. The increase was limited to stage I cervical cancer. But there was no evidence of a lack of screening leading to increasing rates. While the researchers considered it too early to conclude vaccine efficacy in protecting against cancer, these findings merit further study. Could HPV vaccines make HPV infections worse? Besides the vaccine’s unclear effectiveness in cancer prevention, studies further suggest the suppression of the HPV strains targeted by the vaccine may induce more virulent strains. For example, a 2015 study found that vaccinated young adult women had a higher prevalence of high-risk HPV types other than types 16 and 18, putting them at risk for more aggressive cervical and other HPV-related cancers. Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases in China, is the chief scientific officer and co-founder of a Swiss biotech company and former senior medical scientific expert for antiviral drug development at Novartis Pharma in Switzerland. If you or your child suffered harm after receiving the Gardasil HPV vaccine, you may have a legal claim. Please visit Wisner Baum for a free case evaluation. Click here to watch a Gardasil litigation update interview with Wisner Baum Senior Partner Bijan Esfandiari. https://childrenshealthdefense.org/defender/truth-hpv-vaccine-part-3-et/ https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-3.html
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    The Truth About HPV Vaccination, Part 3: Can It Prevent Cervical Cancer?
    There are no valid studies showing the vaccine for the human papillomavirus, or HPV, prevents cervical cancer. However, there are studies suggesting the vaccine could increase the risk of cancer.
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  • The Truth About HPV Vaccination, Part 2: Studies Link the Vaccines to Neurological, Autoimmune Disorders
    Researchers who looked closely into the Gardasil HPV vaccine concluded the risks from the vaccine seem to significantly outweigh the as-yet-unproven long-term benefits.

    The Epoch Times

    Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free.

    By Dr. Yuhong Dong

    Editor’s Note: This second installment in a multi-part series about the human papillomavirus, or HPV, vaccine examines studies that link the vaccines to increased risk of serious neurological and autoimmune disorders. Read Part 1 here.

    Summary of key facts

    A Danish review of 79,102 female and 16,568 male subjects, found human papillomavirus (HPV) vaccines had significantly increased rates of serious nervous system disorders. Postural orthostatic tachycardia syndrome (POTS) and complex regional pain syndrome were judged “definitely associated” with the HPV vaccine.
    A large Danish and Swedish study including nearly 300,000 girls found a significant association between the HPV vaccine and increased rates of Bechet’s syndrome (rate ratio 3.37), Raynaud’s disease (1.67) and type 1 diabetes (1.29).
    A large study including 3 million Danish and Swedish women aged 18 to 44, identified seven adverse events with statistically significant increased risks following HPV vaccination: Hashimoto’s thyroiditis, celiac disease, lupus erythematosus, pemphigus vulgaris, Addison’s disease, Raynaud’s disease and encephalitis, myelitis, or encephalomyelitis.
    A 2017 French study of over 2.2 million young girls found evidence of a 3.78-fold increased risk of Guillain-Barré syndrome (GBS). A 2011 U.S. study found nearly a two-and-a-half to 10 times greater risk of acquiring GBS within six weeks post-Gardasil vaccination.
    While the underlying mechanisms causing these autoimmune reactions are not yet fully understood, some researchers speculate that the sizable overlap in protein sequences between the HPV and the human genome may cause the immune system to attack itself. Others are concerned that the adjuvants (such as aluminum) used to attract the attention of the immune system may be causing harm.
    Neurological and autoimmune disorders

    Danish review found increased nervous system disorder

    In 2020, a group of Danish scientists conducted a systematic review of the overall benefits and harms of HPV vaccines.

    Twenty-four eligible randomized controlled clinical studies were obtained, with a total of 95,670 participants, mostly women, and 49 months mean weighted follow-up.

    Almost all controls were given an active comparator vaccine (typically a hepatitis vaccine with a comparable aluminum-based adjuvant).

    Given that the adjuvant is highly immunogenic by design (it is meant to grab the attention of the immune system), this trial design makes it difficult to detect an excess risk with the HPV vaccines.

    Without true controls (such as a saline placebo), the real risks of HPV vaccination cannot be accurately assessed.

    In the vaccine group, 367 cancers were detected, compared to 490 in the comparator group.

    Younger participants (15 to 29) seemed to benefit more from the vaccine concerning preventing moderate HPV-related intraepithelial neoplasia compared to older participants (ages 21 to 72). Younger participants also had fewer fatal harms.

    Even though the studies were flawed in their design, at four years post-vaccination, those who had received the HPV vaccines had significantly increased rates of serious nervous system disorders: 49%, as well as general harms totaling 7%.

    The serious harms that were judged “definitely associated” with HPV vaccines were postural orthostatic tachycardia syndrome and complex regional pain syndrome. POTS had a nearly twofold increase in the vaccinated group.

    By July 2017, only two-thirds of the results from HPV vaccine trials had been published, and only about half the results had been posted, due to manuscript length limitations, reporting bias and confounding journal articles offering a limited view of trial outcomes.

    This Danish systematic review compiled data from all the HPV trials to offer a summary of the evidence thus far.

    Nevertheless, the investigators acknowledged that despite three years of work, the limitations of their analysis remained. These included reporting bias, incomplete reporting, data fragmentation and limited trial follow-up.

    These investigators similarly note that the trials were powered to assess the benefits of HPV vaccination, not rare harms. The degree to which benefits outweigh risks is therefore unknown.

    They concluded that future research should carefully evaluate the harms following Gardasil 9 compared to Gardasil because the former contains more than double the virus proteins and aluminum-containing adjuvant than the same dose of Gardasil.

    RFK Jr. and Brian Hooker Vax-Unvax
    RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax”

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    Large studies reveal autoimmune events

    In 2009, the HPV4 vaccine was integrated into the Danish childhood vaccination program. Since then, two large cohort studies on the HPV4 vaccine adverse events have been carried out using the hospital-based healthcare registries of Denmark and Sweden.

    The first study in Denmark and Sweden included 296,826 girls aged 10 to 17 who received a total of 696,420 HPV4 vaccine doses.

    The scientists evaluated rate ratios for autoimmune events and found no significant association for 20 out of 23 events.

    They found a significant association between the HPV4 vaccine and Bechet’s syndrome (rate ratio 3.37), Raynaud’s disease (1.67) and type 1 diabetes (1.29).

    But after further review, they concluded that there was insufficient evidence for a causal association, because of the weakness of the signal and the lack of an underlying mechanism to explain biological plausibility.

    In a second large cohort study, the same team expanded their research to more than 3 million Danish and Swedish adult women aged 18 to 44.

    The authors identified seven adverse events with statistically significant increased risks following HPV4 vaccination: Hashimoto’s thyroiditis, celiac disease, lupus erythematosus, pemphigus vulgaris, Addison’s disease, Raynaud’s disease and encephalitis, myelitis or encephalomyelitis.

    After sensitivity analyses, the association between HPV4 vaccination and celiac disease was the most robust finding.

    Celiac disease is a condition where a person’s immune system attacks the body’s own gut after eating gluten.

    As the graph below shows, the scientists used two risk periods after HPV4 vaccination: the first 180 days and after.

    1 time since first dose HPV4 vaccine coeliac cases
    Time since the first dose of the HPV4 vaccine for vaccinated coeliac cases in a cohort of Danish and Swedish women. Credit: Journal of Internal Medicine
    The authors noted that the observed 56% increased risk of celiac disease “was strong, and the increase was strikingly similar in both risk periods after vaccination.”

    Celiac disease is underdiagnosed in Denmark.

    So one possible explanation is that vaccination visits allow a chance for this and other conditions to be diagnosed and explored.

    This explanation suggests that the association between the HPV vaccine and autoimmune disorders may be coincidental.

    However, given the lack of any real control groups in these studies, as well as the growing body of scientific literature from countries around the world showing problems with the HPV vaccine, dismissing these safety signals as coincidence seems short-sighted.

    Large French study and U.S. VAERS study identify risks of Guillain-Barré Syndrome

    The concern about autoimmune disease adverse events has contributed to low HPV vaccination uptake in France.

    A 2017 study of over 2.2 million young girls in France found troubling evidence of a link with Guillain-Barré syndrome. GBS is a condition that arises when our own antibodies attack the nerves.

    The incidence of GBS was found to be 1.4 per 100,000 person-years among the vaccinated girls compared to 0.4 per 100,000 among the unvaccinated, resulting in an increased risk of GBS of more than 200%.

    The association appeared to be “particularly marked in the first months following vaccination.”

    This finding is corroborated by the pattern of adverse reactions reported worldwide. Data from a large number of case reports document similar serious adverse events associated with Gardasil administration, with nervous system disorders of autoimmune origin being the most frequently reported.

    A 2011 U.S. study found that the estimated weekly reporting rate of post-Gardasil GBS within the first six weeks (6.6 per 10,000,000) was higher than in the general population, and higher than post-Menactra and post-influenza vaccinations.

    In particular, there was nearly a two-and-a-half to 10 times greater risk of acquiring GBS within six weeks after vaccination, compared to the general population.

    Additionally, the study found Gardasil vaccination was associated with approximately eight-and-a-half times more emergency department visits, 12.5 times more hospitalizations, 10 times more life-threatening events and 26.5 times more disability than the Menactra vaccination.

    Plausible mechanisms of harm

    Despite the conflicting data in the scientific literature to date, it is clear that the HPV vaccines can cause autoimmune disorders in susceptible people. But how?

    Autoimmunity has been reported as a complication of natural infection as well as virus vaccination. This phenomenon has been observed with many viruses, including the Epstein-Barr virus, COVID-19 and HPV.

    According to a 2019 study, the HPV vaccine contains epitopes — portions of the virus proteins — that overlap with the human proteins.

    This means that if we develop antibodies to those viruses, we may also generate autoantibodies to our own cells, which is the root cause of autoimmune dysfunction.

    The study showed that most of the immunoreactive HPV L1 epi­topes are overlapping peptides present in human proteins.

    The authors explained that this “unexpected enormous size of the peptide overlap between the HPV epitopes and human proteins” is relevant, and may be why a wide variety of autoimmune diseases have been reported post-HPV vaccination, including ovarian failure, systemic lupus erythematosus, breast cancer and sudden death, among others.

    Why some people develop these conditions and others do not is unclear.

    The authors suggest that vaccines should target the few peptides that do not overlap with human proteins, but which do overlap with the other HPVs.

    Despite this overlap and the potential for causing autoimmune disease, medical doctors usually ignore or dismiss the connection. We are told that these diseases are rare.

    The human body has something called immune tolerance. This protects a person’s immune system against attacking itself. Therefore, HPV infection is also “immune tolerated,” which means it lays dormant for some time until it becomes cancerous.

    HPV vaccination was actually designed with this immune tolerance in mind.

    Given the human body’s built-in defenses against autoimmune conditions, vaccinology requires an immunogenic catalyst to get the body’s attention. This is the job of an adjuvant.

    An adjuvant is an ingredient used in a vaccine that the body recognizes as foreign. It is added to vaccines so that the body will mount a stronger immune response.

    The idea is that in attacking the adjuvant, the body will also recognize other vaccine ingredients (in this case, purified HPV proteins).

    In addition, the antigen dose is much higher than in natural infections and the capsids in the vaccine are directly exposed to systemic immune responses as opposed to the virus staying relatively hidden within the natural barrier of the skin following infection.

    The vaccine was well-designed to trigger an immune response, but this advantage may come at a cost: Generating antibodies to HPV proteins through vaccination could, theoretically, set the stage for an autoimmune attack.

    Link between HPV-vaccine-associated nervous system dysfunction and autoimmunity

    A December 2022 Danish and German study was designed to elucidate a possible mechanism of harm.

    The lead author, Dr. Jesper Mehlsen, a specialist in treating autoimmune conditions, noted that the HPV major capsid L1s antigen resembles human autonomic nerve receptors, including G-protein coupled receptors (GPCR).

    According to the researchers, in the past several years, case series of suspected vaccination side effects have pointed to three disease entities: POTS, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and complex regional pain syndrome. These syndromes may be associated with neuroendocrine GPCR antibodies.

    From 2011 to 2018, researchers saw 845 patients (839 females, six males) with suspected side effects following the HPV4 vaccine. The control group included vaccinated people without side effects.

    Moderate to severe fatigue was recorded in 83.3% of the patients but in none of the controls.

    A high prevalence of symptoms, such as dizziness (91%), heart palpitations (71%), nausea (80%) and hyperactive bladder suggested that the patients were experiencing some kind of autonomic dysfunction.

    Autonomic dysfunction occurs when the part of the nervous system that controls well-being and balance does not function properly.

    2 most frequent symptoms hpv vaccine
    Most frequent symptoms reported by 612 patients in Denmark. Credit: Journal of Autoimmunity
    Twenty-four percent higher antinuclear antibodies (ANA, a common type of autoantibodies) were found in patients, suggesting possible autoimmunity.

    3 antinuclear antibodies HPV vaccines
    A larger proportion of the symptomatic patients were found with a common type of autoantibodies compared to healthy controls. Credit: Journal of Autoimmunity
    Antibodies against the adrenergic ß-2-receptor and muscarinic M-2 receptors were also found significantly higher in patients.

    Many of the symptoms, including immune activation and autonomic dysregulation, could be mediated or aggravated by dysregulated autoantibodies against adrenergic receptors and impaired peripheral adrenergic function.

    The authors suggested that girls and women with probable side effects of HPV vaccination have symptoms and biological markers compatible with an autoimmune disease closely resembling that seen in ME/CFS.

    Interestingly, people who already had HPV infections at some point appeared to be at greater risk for adverse events following vaccination.

    The authors noted that “prior disease may precondition some individuals for vaccine-related adverse events.”

    They also noted that some of the adverse events resembled long-COVID symptoms.

    Universal HPV vaccination called into question

    Academic researcher at the University of British Columbia, Lucija Tomljenovic, and neuroscientist Christopher Shaw, who have closely looked into Gardasil, have argued that the risks from the vaccine seem to significantly outweigh the as-yet-unproven long-term benefits.

    In a 2012 comment published in the American Journal of Public Health, they took issue with “incomplete and inaccurate” data and poorly designed trials.

    Vaccination is unjustified if the vaccine carries any substantial risk, as healthy teenagers face little to no risk of dying from cervical cancer.

    Risk-benefit analyses must be conducted to ascertain the overall balance of benefits and harms on both individual and societal levels.

    Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases in China, is the chief scientific officer and co-founder of a Swiss biotech company and former senior medical scientific expert for antiviral drug development at Novartis Pharma in Switzerland.

    If you or your child suffered harm after receiving the Gardasil HPV vaccine, you may have a legal claim. Please visit Wisner Baum for a free case evaluation. Click here to watch a Gardasil litigation update interview with Wisner Baum Senior Partner Bijan Esfandiari.

    The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children's Health Defense.

    https://childrenshealthdefense.org/defender/truth-hpv-vaccine-part-2-et/

    https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-2.html
    The Truth About HPV Vaccination, Part 2: Studies Link the Vaccines to Neurological, Autoimmune Disorders Researchers who looked closely into the Gardasil HPV vaccine concluded the risks from the vaccine seem to significantly outweigh the as-yet-unproven long-term benefits. The Epoch Times Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. By Dr. Yuhong Dong Editor’s Note: This second installment in a multi-part series about the human papillomavirus, or HPV, vaccine examines studies that link the vaccines to increased risk of serious neurological and autoimmune disorders. Read Part 1 here. Summary of key facts A Danish review of 79,102 female and 16,568 male subjects, found human papillomavirus (HPV) vaccines had significantly increased rates of serious nervous system disorders. Postural orthostatic tachycardia syndrome (POTS) and complex regional pain syndrome were judged “definitely associated” with the HPV vaccine. A large Danish and Swedish study including nearly 300,000 girls found a significant association between the HPV vaccine and increased rates of Bechet’s syndrome (rate ratio 3.37), Raynaud’s disease (1.67) and type 1 diabetes (1.29). A large study including 3 million Danish and Swedish women aged 18 to 44, identified seven adverse events with statistically significant increased risks following HPV vaccination: Hashimoto’s thyroiditis, celiac disease, lupus erythematosus, pemphigus vulgaris, Addison’s disease, Raynaud’s disease and encephalitis, myelitis, or encephalomyelitis. A 2017 French study of over 2.2 million young girls found evidence of a 3.78-fold increased risk of Guillain-Barré syndrome (GBS). A 2011 U.S. study found nearly a two-and-a-half to 10 times greater risk of acquiring GBS within six weeks post-Gardasil vaccination. While the underlying mechanisms causing these autoimmune reactions are not yet fully understood, some researchers speculate that the sizable overlap in protein sequences between the HPV and the human genome may cause the immune system to attack itself. Others are concerned that the adjuvants (such as aluminum) used to attract the attention of the immune system may be causing harm. Neurological and autoimmune disorders Danish review found increased nervous system disorder In 2020, a group of Danish scientists conducted a systematic review of the overall benefits and harms of HPV vaccines. Twenty-four eligible randomized controlled clinical studies were obtained, with a total of 95,670 participants, mostly women, and 49 months mean weighted follow-up. Almost all controls were given an active comparator vaccine (typically a hepatitis vaccine with a comparable aluminum-based adjuvant). Given that the adjuvant is highly immunogenic by design (it is meant to grab the attention of the immune system), this trial design makes it difficult to detect an excess risk with the HPV vaccines. Without true controls (such as a saline placebo), the real risks of HPV vaccination cannot be accurately assessed. In the vaccine group, 367 cancers were detected, compared to 490 in the comparator group. Younger participants (15 to 29) seemed to benefit more from the vaccine concerning preventing moderate HPV-related intraepithelial neoplasia compared to older participants (ages 21 to 72). Younger participants also had fewer fatal harms. Even though the studies were flawed in their design, at four years post-vaccination, those who had received the HPV vaccines had significantly increased rates of serious nervous system disorders: 49%, as well as general harms totaling 7%. The serious harms that were judged “definitely associated” with HPV vaccines were postural orthostatic tachycardia syndrome and complex regional pain syndrome. POTS had a nearly twofold increase in the vaccinated group. By July 2017, only two-thirds of the results from HPV vaccine trials had been published, and only about half the results had been posted, due to manuscript length limitations, reporting bias and confounding journal articles offering a limited view of trial outcomes. This Danish systematic review compiled data from all the HPV trials to offer a summary of the evidence thus far. Nevertheless, the investigators acknowledged that despite three years of work, the limitations of their analysis remained. These included reporting bias, incomplete reporting, data fragmentation and limited trial follow-up. These investigators similarly note that the trials were powered to assess the benefits of HPV vaccination, not rare harms. The degree to which benefits outweigh risks is therefore unknown. They concluded that future research should carefully evaluate the harms following Gardasil 9 compared to Gardasil because the former contains more than double the virus proteins and aluminum-containing adjuvant than the same dose of Gardasil. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now Large studies reveal autoimmune events In 2009, the HPV4 vaccine was integrated into the Danish childhood vaccination program. Since then, two large cohort studies on the HPV4 vaccine adverse events have been carried out using the hospital-based healthcare registries of Denmark and Sweden. The first study in Denmark and Sweden included 296,826 girls aged 10 to 17 who received a total of 696,420 HPV4 vaccine doses. The scientists evaluated rate ratios for autoimmune events and found no significant association for 20 out of 23 events. They found a significant association between the HPV4 vaccine and Bechet’s syndrome (rate ratio 3.37), Raynaud’s disease (1.67) and type 1 diabetes (1.29). But after further review, they concluded that there was insufficient evidence for a causal association, because of the weakness of the signal and the lack of an underlying mechanism to explain biological plausibility. In a second large cohort study, the same team expanded their research to more than 3 million Danish and Swedish adult women aged 18 to 44. The authors identified seven adverse events with statistically significant increased risks following HPV4 vaccination: Hashimoto’s thyroiditis, celiac disease, lupus erythematosus, pemphigus vulgaris, Addison’s disease, Raynaud’s disease and encephalitis, myelitis or encephalomyelitis. After sensitivity analyses, the association between HPV4 vaccination and celiac disease was the most robust finding. Celiac disease is a condition where a person’s immune system attacks the body’s own gut after eating gluten. As the graph below shows, the scientists used two risk periods after HPV4 vaccination: the first 180 days and after. 1 time since first dose HPV4 vaccine coeliac cases Time since the first dose of the HPV4 vaccine for vaccinated coeliac cases in a cohort of Danish and Swedish women. Credit: Journal of Internal Medicine The authors noted that the observed 56% increased risk of celiac disease “was strong, and the increase was strikingly similar in both risk periods after vaccination.” Celiac disease is underdiagnosed in Denmark. So one possible explanation is that vaccination visits allow a chance for this and other conditions to be diagnosed and explored. This explanation suggests that the association between the HPV vaccine and autoimmune disorders may be coincidental. However, given the lack of any real control groups in these studies, as well as the growing body of scientific literature from countries around the world showing problems with the HPV vaccine, dismissing these safety signals as coincidence seems short-sighted. Large French study and U.S. VAERS study identify risks of Guillain-Barré Syndrome The concern about autoimmune disease adverse events has contributed to low HPV vaccination uptake in France. A 2017 study of over 2.2 million young girls in France found troubling evidence of a link with Guillain-Barré syndrome. GBS is a condition that arises when our own antibodies attack the nerves. The incidence of GBS was found to be 1.4 per 100,000 person-years among the vaccinated girls compared to 0.4 per 100,000 among the unvaccinated, resulting in an increased risk of GBS of more than 200%. The association appeared to be “particularly marked in the first months following vaccination.” This finding is corroborated by the pattern of adverse reactions reported worldwide. Data from a large number of case reports document similar serious adverse events associated with Gardasil administration, with nervous system disorders of autoimmune origin being the most frequently reported. A 2011 U.S. study found that the estimated weekly reporting rate of post-Gardasil GBS within the first six weeks (6.6 per 10,000,000) was higher than in the general population, and higher than post-Menactra and post-influenza vaccinations. In particular, there was nearly a two-and-a-half to 10 times greater risk of acquiring GBS within six weeks after vaccination, compared to the general population. Additionally, the study found Gardasil vaccination was associated with approximately eight-and-a-half times more emergency department visits, 12.5 times more hospitalizations, 10 times more life-threatening events and 26.5 times more disability than the Menactra vaccination. Plausible mechanisms of harm Despite the conflicting data in the scientific literature to date, it is clear that the HPV vaccines can cause autoimmune disorders in susceptible people. But how? Autoimmunity has been reported as a complication of natural infection as well as virus vaccination. This phenomenon has been observed with many viruses, including the Epstein-Barr virus, COVID-19 and HPV. According to a 2019 study, the HPV vaccine contains epitopes — portions of the virus proteins — that overlap with the human proteins. This means that if we develop antibodies to those viruses, we may also generate autoantibodies to our own cells, which is the root cause of autoimmune dysfunction. The study showed that most of the immunoreactive HPV L1 epi­topes are overlapping peptides present in human proteins. The authors explained that this “unexpected enormous size of the peptide overlap between the HPV epitopes and human proteins” is relevant, and may be why a wide variety of autoimmune diseases have been reported post-HPV vaccination, including ovarian failure, systemic lupus erythematosus, breast cancer and sudden death, among others. Why some people develop these conditions and others do not is unclear. The authors suggest that vaccines should target the few peptides that do not overlap with human proteins, but which do overlap with the other HPVs. Despite this overlap and the potential for causing autoimmune disease, medical doctors usually ignore or dismiss the connection. We are told that these diseases are rare. The human body has something called immune tolerance. This protects a person’s immune system against attacking itself. Therefore, HPV infection is also “immune tolerated,” which means it lays dormant for some time until it becomes cancerous. HPV vaccination was actually designed with this immune tolerance in mind. Given the human body’s built-in defenses against autoimmune conditions, vaccinology requires an immunogenic catalyst to get the body’s attention. This is the job of an adjuvant. An adjuvant is an ingredient used in a vaccine that the body recognizes as foreign. It is added to vaccines so that the body will mount a stronger immune response. The idea is that in attacking the adjuvant, the body will also recognize other vaccine ingredients (in this case, purified HPV proteins). In addition, the antigen dose is much higher than in natural infections and the capsids in the vaccine are directly exposed to systemic immune responses as opposed to the virus staying relatively hidden within the natural barrier of the skin following infection. The vaccine was well-designed to trigger an immune response, but this advantage may come at a cost: Generating antibodies to HPV proteins through vaccination could, theoretically, set the stage for an autoimmune attack. Link between HPV-vaccine-associated nervous system dysfunction and autoimmunity A December 2022 Danish and German study was designed to elucidate a possible mechanism of harm. The lead author, Dr. Jesper Mehlsen, a specialist in treating autoimmune conditions, noted that the HPV major capsid L1s antigen resembles human autonomic nerve receptors, including G-protein coupled receptors (GPCR). According to the researchers, in the past several years, case series of suspected vaccination side effects have pointed to three disease entities: POTS, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and complex regional pain syndrome. These syndromes may be associated with neuroendocrine GPCR antibodies. From 2011 to 2018, researchers saw 845 patients (839 females, six males) with suspected side effects following the HPV4 vaccine. The control group included vaccinated people without side effects. Moderate to severe fatigue was recorded in 83.3% of the patients but in none of the controls. A high prevalence of symptoms, such as dizziness (91%), heart palpitations (71%), nausea (80%) and hyperactive bladder suggested that the patients were experiencing some kind of autonomic dysfunction. Autonomic dysfunction occurs when the part of the nervous system that controls well-being and balance does not function properly. 2 most frequent symptoms hpv vaccine Most frequent symptoms reported by 612 patients in Denmark. Credit: Journal of Autoimmunity Twenty-four percent higher antinuclear antibodies (ANA, a common type of autoantibodies) were found in patients, suggesting possible autoimmunity. 3 antinuclear antibodies HPV vaccines A larger proportion of the symptomatic patients were found with a common type of autoantibodies compared to healthy controls. Credit: Journal of Autoimmunity Antibodies against the adrenergic ß-2-receptor and muscarinic M-2 receptors were also found significantly higher in patients. Many of the symptoms, including immune activation and autonomic dysregulation, could be mediated or aggravated by dysregulated autoantibodies against adrenergic receptors and impaired peripheral adrenergic function. The authors suggested that girls and women with probable side effects of HPV vaccination have symptoms and biological markers compatible with an autoimmune disease closely resembling that seen in ME/CFS. Interestingly, people who already had HPV infections at some point appeared to be at greater risk for adverse events following vaccination. The authors noted that “prior disease may precondition some individuals for vaccine-related adverse events.” They also noted that some of the adverse events resembled long-COVID symptoms. Universal HPV vaccination called into question Academic researcher at the University of British Columbia, Lucija Tomljenovic, and neuroscientist Christopher Shaw, who have closely looked into Gardasil, have argued that the risks from the vaccine seem to significantly outweigh the as-yet-unproven long-term benefits. In a 2012 comment published in the American Journal of Public Health, they took issue with “incomplete and inaccurate” data and poorly designed trials. Vaccination is unjustified if the vaccine carries any substantial risk, as healthy teenagers face little to no risk of dying from cervical cancer. Risk-benefit analyses must be conducted to ascertain the overall balance of benefits and harms on both individual and societal levels. Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases in China, is the chief scientific officer and co-founder of a Swiss biotech company and former senior medical scientific expert for antiviral drug development at Novartis Pharma in Switzerland. If you or your child suffered harm after receiving the Gardasil HPV vaccine, you may have a legal claim. Please visit Wisner Baum for a free case evaluation. Click here to watch a Gardasil litigation update interview with Wisner Baum Senior Partner Bijan Esfandiari. The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children's Health Defense. https://childrenshealthdefense.org/defender/truth-hpv-vaccine-part-2-et/ https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-2.html
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    The Truth About HPV Vaccination, Part 2: Studies Link the Vaccines to Neurological, Autoimmune Disorders
    Researchers who looked closely into the Gardasil HPV vaccine concluded the risks from the vaccine seem to significantly outweigh the as-yet-unproven long-term benefits.
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  • The Truth About HPV Vaccination, Part 1: How Safe Is It, Really?
    This first installment in a multi-part series about the human papillomavirus, or HPV, vaccine explores peer-reviewed scientific literature that reveals serious safety concerns about a vaccine widely regarded as safe.

    The Epoch Times

    Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free.

    By Yuhong Dong

    The decline of public trust in COVID-19 vaccines significantly impacts vaccination rates against routine childhood diseases. This multiple-part series explores the international research done over the past two decades on the human papillomavirus (HPV) vaccine — believed to be one of the most effective vaccines developed to date.

    Summary of Key Facts

    This multiple-part series offers a thorough analysis of concerns raised about HPV vaccination following the global HPV campaign, which commenced in 2006.
    In the U.S., the HPV vaccine was reported to have a disproportionately higher percentage of adverse events of fainting and blood clots in the veins. The U.S. Food and Drug Administration (FDA) acknowledges that fainting can happen following the HPV vaccine, and recommends sitting or lying down to get the shot, then waiting for 15 minutes afterward.
    International scientists found that the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) logged a substantial increase in reports of premature ovarian failure from 1.4 per year before 2006 to 22.2 per year after the HPV vaccine approval, yielding a Proportional Reporting Ratio of 46.1.
    The HPV vaccine is widely regarded as one of the most effective vaccines developed to date. Nevertheless, safety issues have been raised following its approval, and in response, additional research has been published and litigation has been brought on behalf of those with a vaccine injury.

    In this HPV vaccine series, Parts I and II explain how the vaccine works and the evidence suggesting there may be legitimate safety concerns. The remaining parts present questions about real-world vaccine effectiveness and identify specific ingredients which may pose harm.

    The information presented here is drawn from peer-reviewed scientific literature from the U.S., Australia, Denmark, Sweden, France and Japan, as well as statistics published by public health agencies in each of these countries.

    More than 100 hours of research and internal peer review among scientists with experience in infectious diseases, virology, clinical trials and vaccine epidemiology have been invested in presenting this summary of the evidence.

    Large registry-based studies have identified plausible associations between HPV vaccination and autoimmune conditions, including premature ovarian insufficiency or premature ovarian failure, Guillain-Barré syndrome (GBS), postural orthostatic tachycardia syndrome and chronic regional pain syndrome.

    While it is easy to be enthusiastic about recent advances in human vaccine technology, we should keep in mind that achieving real and lasting good health is much more than just the absence of a certain virus.

    RFK Jr. and Brian Hooker Vax-Unvax
    RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax”

    Order Now

    What is HPV?

    According to the CDC, HPV is the most common sexually transmitted infection in the U.S.

    HPV is a small DNA virus infecting human cutaneous epithelial cells in the mucosa and skin. More than 150 strains of the HPV virus have been identified.

    HPV infection is so common that the majority of sexually active people will get it at some point in their lives, even if they have only one or very few sexual partners. It can spread through sexual intercourse and oral sex. It can also pass between people through skin-to-skin contact, even by people who have no symptoms.

    HPV infection causes genital warts, some of which can turn into cancer. For the most part, however, HPV infection is benign. More than 90% of HPV infections cause no clinical symptoms and are self-limited, meaning the virus is cleared by the body via natural immunological defenses.

    HPV-associated cancers

    High-risk HPV types (types 16, 18 and others) can cause cervical cell abnormalities that are precursors to cancers.

    Type 16 is associated with approximately 50% of cervical cancers worldwide, and types 16 and 18 together are linked to 66% of cervical cancers.

    An additional five high-risk types, 31, 33, 45, 52 and 58, are linked with another 15% of cervical cancers and 11% of all HPV-associated cancers.

    Infection with a high-risk HPV type is associated with a higher chance of the development of cervical cancer but, by itself, HPV infection is not the sole risk factor to cause cancer. There are many other reasons, as discussed in this paper.

    Given the prevalence of infection, it is unsurprising that globally, cervical cancer is the fourth most common cancer in women. In 2018, an estimated 570,000 women were diagnosed with cervical cancer worldwide and more than 300,000 died of the disease.

    In the U.S., nearly 50,000 new HPV-associated cancers occur annually, with women infected at a slightly higher rate than men.

    But in 9 out of 10 cases, HPV goes away within two years without causing health problems.

    Only persistent HPV infections may lead to cancer. These infections evade the immune system’s innate cell-mediated defenses.

    The incidence of cervical cancer can be controlled as a result of the implementation of routine testing and screening, including Pap and DNA tests.

    HPV vaccines

    Three HPV vaccines — bivalent HPV vaccine (Cervarix, 2vHPV), quadrivalent HPV vaccine (Gardasil, 4vHPV or HPV4) and 9-valent HPV vaccine (Gardasil 9, 9vHPV) — have been licensed by the FDA.

    The HPV vaccine uses recombinant technology to assemble the shell of the virus — L1 capsid protein. These viral-like particles do not contain the virus genome and are not infectious.

    Cervarix, developed by GlaxoSmithKline, is a bivalent vaccine against HPV types 16 and 18, that was pulled from the U.S. market in 2016 due to “very low market demand.”

    Merck’s original Gardasil vaccine was designed to prevent infections from four strains (types 6, 11, 16 and 18).

    On June 8, 2006, after the FDA’s fast-tracked review, Gardasil was approved for use in females ages 9 to 26 for the prevention of cervical, vulvar and vaginal cancers.

    According to the label accompanying the vaccine, the ingredients in Merck’s first Gardasil vaccine were proteins of HPV, amorphous aluminum hydroxyphosphate sulfate, yeast protein, sodium chloride, L-histidine, polysorbate 80, sodium borate and water for injection.

    On Oct. 16, 2009, the FDA approved Gardasil (HPV4) for use in boys ages 9 through 26 for the prevention of genital warts caused by HPV types 6 and 11, but not for cancer.

    In 2010, it approved Gardasil for the prevention of anal cancer in males and females ages 9 to 26.

    Four years later, the FDA approved an updated vaccine, Merck’s Gardasil 9, for use in girls ages 9 to 26 and boys ages 9 to 15 for the prevention of cervical, vaginal and anal cancers.

    Gardasil 9 contains the same ingredients as Gardasil, but offers protection against nine HPV strains, adding five additional types (HPV types 31, 33, 45, 52 and 58).

    The current HPV vaccination schedule recommended by the CDC is two doses for both boys and girls aged 11 or 12. However, it is approved for children as young as 9. The second dose is given 6 to 12 months after the first.

    For those aged 15 and above, a three-dose schedule is implemented at one- to two-month and six-month intervals, although antibody-level studies suggest that two doses are sufficient.

    The vaccine prompts the body to produce neutralizing antibodies against HPV. Antibody responses appear to peak seven months after the first dose (or one month after the third dose). The vaccine-induced antibody levels appear to be 10 to 100 times higher than those after natural infection.

    The high vaccine effectiveness (90 to 98%) against the fast-growing, abnormal cells which may cause precancerous lesions in people ages 16 to 26 suggested that the best timing for vaccination was to give it to patients before they became sexually active.

    HPV VAERS reports from 2 large countries

    U.S. HPV vaccine adverse events

    On Aug. 19, 2009, the Journal of the American Medical Association published an article authored by scientists from the FDA and CDC that reviewed the safety data for Gardasil for adverse events reported to VAERS between June 2006 through December 2008.

    During that time, there were 12,424 reports of adverse events. Of these, 772 (6.2%) were serious.

    VAERS is a passive surveillance system, which is subject to multiple limitations, including underreporting, unconfirmed diagnosis, lack of denominator data and no unbiased comparison groups.

    Nevertheless, it is a useful and important tool for detecting postmarket safety issues with vaccines.

    A disproportionately high percentage of Gardasil VAERS reports were of syncope (fainting) and venous thromboembolic events (blood clots in the veins) compared with other vaccines. There were 8.2 syncope events per 100,000 HPV doses and 0.2 venous thromboembolic events per 100,000 HPV doses reported, respectively.

    The Gardasil package insert includes a warning about fainting, fever, dizziness, nausea and headaches (page 1) and notes at least the following adverse reactions reported during postmarketing surveillance (section 6.2): Guillain-Barré syndrome, transverse myelitis, motor neuron disease, venous thromboembolic events, pancreatitis and autoimmune disorders.

    Australia HPV vaccines adverse events

    In 2007, Australia reported an annual adverse drug reaction rate of 7.3/100,000, the highest since 2003, representing an 85% increase from 2006.

    Per the analysis of the Adverse Drug Reactions System database by the Australian Department of Health and Aging, this increase was “almost entirely due to” reports following the national rollout of the three-dose HPV vaccination program for young females in April 2007; 705 of the 1,538 adverse drug reactions reported that year were from the Gardasil vaccine.

    1 vaccine adverse events australia chart
    In Australia, the ADR increase in 2007 was almost entirely due to the three-dose HPV vaccination program for females aged 12 to 26 years in April 2007. Credit: Australian Government Department of Health and Aged Care.
    Moreover, though people may take different vaccines other than HPV, the HPV vaccine was the only suspected vaccine to cause adverse reactions in 96% of records. Twenty-nine percent had causality ratings of “certain” or “probable” and 6% were defined as “serious.”

    2 vaccine types vaccine suspected chart
    In these HPV-induced ADRs, 674 were suspected to be related to HPV vaccines, 203 had causality ratings of “certain” or “probable,” and 43 were defined as “serious.” Credit: Australian Government Department of Health and Aged Care.
    Japan withdraws recommendation, vaccine acceptance plunged

    In 2013, the Japanese raised concerns about a variety of widely reported post-vaccination serious adverse events. This led the government to suspend recommending the HPV vaccine for six years. Vaccine acceptance of HPV in Japan plunged significantly after 2013, from 42.9% to 14.3%, or from 65.4% to 3.9%.

    Researchers around the world also started to investigate HPV safety. A World Health Organization (WHO) position paper released on July 14, 2017, concluded that the HPV vaccines were “extremely safe.”

    The same report estimated approximately 1.7 cases of anaphylaxis per million HPV doses, that no association with GBS was found, and that syncope (fainting) was “established as a common anxiety or stress-related reaction to the injection.”

    In the spring of 2022, Japan announced it was relaunching its HPV vaccination drive. Mainstream news outlets reported that for thousands of women, the cost of caution may have led to preventable HPV-induced cancers and an estimated 5,000 to 5,700 deaths.

    However, a true risk-benefit analysis would also consider the number of serious adverse events prevented by putting the program on hold. The question remains: Was Japan’s caution warranted, or should their national vaccination program have continued?

    Ovarian insufficiency

    Concerns that the vaccine may be negatively affecting fertility have been detailed in the scientific literature.

    In 2014, a peer-reviewed case series describing premature ovarian failure among Australian women following HPV vaccination was published in the Journal of Investigative Medicine.

    This prompted other researchers to systematically examine the VAERS data to see if there was a connection between premature ovarian failure and Gardasil. Their study found a “potential safety signal” and concluded that “further investigations are warranted.”

    VAERS analysis on ovarian failure

    Two recent publications based on VAERS reports (first study, second study) found that events with a probable autoimmune background were significantly more frequent after HPV vaccination compared to other vaccinations.

    The team of international scientists that did the second study evaluated reports between 1990 and 2018. They found that among the 228,341 premature ovarian failure reports, 0.1% was considered to be associated with HPV vaccination with a median age of 15 years and the time to onset was 20.5 days following vaccination.

    The primary symptoms were amenorrhea (80.4%) and premature menopause (15.3%).

    Most strikingly, the mean number of premature ovarian failure cases increased significantly from 1.4 per year prior to 2006 to 22.2 per year after the HPV vaccine was approved, with a proportional reporting ratio of 46.

    The investigators noted that the WHO and CDC declared the HPV vaccine safe regardless of lacking adequate research into safety concerns.

    For example, the authors note that in a CDC-sponsored VAERS study, 17 cases of premature ovarian failure were identified but 15 were excluded due to insufficient information to confirm the diagnosis. A separate observational study using the Vaccine Safety Datalink found no increased risk.

    But this study was too underpowered to detect a signal. In addition, a cross-sectional survey study using National Health and Nutrition Examination Survey data relied on an inaccurate measurement of premature ovarian failure and self-reported HPV vaccination.

    In summary, the researchers detected a strong safety signal even after accounting for a potential upswing in reports due to media coverage after the product launch (they refer to this as “notoriety bias”).

    Because VAERS is a passive reporting system, the data may be incomplete and are often unconfirmed by physicians. Therefore, this study cannot provide a definitive link between HPV vaccination and premature ovarian insufficiency or premature ovarian failure but does generate a hypothetical link.

    The authors of the second study conclude by insisting that “this signal warrants well-designed and appropriate epidemiological research.” They note that “if the signal is confirmed, the risk is small compared to the lifetime risk of cervical cancer.”

    However, the benefit-risk profile on an individual level is not uniform.

    Given the health impacts of premature ovarian insufficiency and premature ovarian failure — some of which may be irreversible — and the declining mortality rate for cervical cancer even in the prevaccine era, the risk-benefit profile for HPV vaccination remains unclear.

    3 case reports on ovarian insufficiency

    In the 2014 investigation mentioned above, a general practitioner in Australia noticed that three girls developed premature ovarian insufficiency following HPV4 vaccination.

    As a result of vaccination, each of the girls (ages 16, 16 and 18) had been prescribed oral contraception to treat menstrual cycle irregularities. Typically, women present with amenorrhea (no periods) or oligomenorrhea (infrequent periods) as the initial symptom of premature ovarian insufficiency.

    One girl had irregular periods following three doses of HPV vaccination. She then became amenorrheic and was diagnosed with premature ovarian insufficiency.

    Another girl’s periods were “like clockwork” until after the third HPV dose, which she received at age 15. Her first cycle after being vaccinated for the third time started two weeks late, and her next cycle was two months late. The final cycle began nine months later. The patient had no family history of early menopause.

    She was diagnosed with premature ovarian failure at 16. Lab work found hormone levels consistent with those of postmenopausal women, but her bone mineral density was normal.

    The authors of this case series noted that in preclinical studies of HPV4, the five-week-old rats only conceived one litter and the only available toxicology studies appear to be on the male rodent reproductive system.

    However, only two of three doses were administered prior to mating, and the overall fecundity was 95%, slightly lower than the control rats (98%) that received no vaccination prior to mating.

    The dose tolerance recommendations were based on an average weight of 50 kilograms for an adolescent girl but failed to take into account that HPV4 is administered to girls ages 9 to 13 years, who range in weight from 28 to 46 kilograms.

    Danish retrospective cohort study finds no link

    A 2021 study also evaluated premature ovarian insufficiency in a nationwide cohort of nearly 1 million Danish females ages 11 to 34 years.

    The researchers used Cox proportional hazard regression to detect an increased risk of premature ovarian insufficiency diagnosis by HPV4 vaccination status during the years 2007-2016. The hazard ratio for premature ovarian insufficiency (vaccinated versus unvaccinated) was 0.96.

    One limitation was that data on age at menarche (first menstruation) and oral contraceptive use were not available. Girls who had not yet reached menarche would not be at risk for premature ovarian insufficiency, of course.

    The authors excluded girls under age 15 in a sensitivity analysis and still found no signal, concluding that no association was found between HPV4 vaccination and premature ovarian insufficiency.

    Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases from China, is the chief scientific officer and co-founder of a Swiss biotech company and a former senior medical scientific expert for antiviral drug development at Novartis Pharma in Switzerland.

    If you or your child suffered harm after receiving the Gardasil HPV vaccine, you may have a legal claim. Please visit Wisner Baum for a free case evaluation. Click here to watch a Gardasil litigation update interview with Wisner Baum Senior Partner Bijan Esfandiari.

    The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children's Health Defense.

    https://childrenshealthdefense.org/defender/hpv-vaccine-safety-concerns-part-1-et/


    https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-1.html
    The Truth About HPV Vaccination, Part 1: How Safe Is It, Really? This first installment in a multi-part series about the human papillomavirus, or HPV, vaccine explores peer-reviewed scientific literature that reveals serious safety concerns about a vaccine widely regarded as safe. The Epoch Times Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. By Yuhong Dong The decline of public trust in COVID-19 vaccines significantly impacts vaccination rates against routine childhood diseases. This multiple-part series explores the international research done over the past two decades on the human papillomavirus (HPV) vaccine — believed to be one of the most effective vaccines developed to date. Summary of Key Facts This multiple-part series offers a thorough analysis of concerns raised about HPV vaccination following the global HPV campaign, which commenced in 2006. In the U.S., the HPV vaccine was reported to have a disproportionately higher percentage of adverse events of fainting and blood clots in the veins. The U.S. Food and Drug Administration (FDA) acknowledges that fainting can happen following the HPV vaccine, and recommends sitting or lying down to get the shot, then waiting for 15 minutes afterward. International scientists found that the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) logged a substantial increase in reports of premature ovarian failure from 1.4 per year before 2006 to 22.2 per year after the HPV vaccine approval, yielding a Proportional Reporting Ratio of 46.1. The HPV vaccine is widely regarded as one of the most effective vaccines developed to date. Nevertheless, safety issues have been raised following its approval, and in response, additional research has been published and litigation has been brought on behalf of those with a vaccine injury. In this HPV vaccine series, Parts I and II explain how the vaccine works and the evidence suggesting there may be legitimate safety concerns. The remaining parts present questions about real-world vaccine effectiveness and identify specific ingredients which may pose harm. The information presented here is drawn from peer-reviewed scientific literature from the U.S., Australia, Denmark, Sweden, France and Japan, as well as statistics published by public health agencies in each of these countries. More than 100 hours of research and internal peer review among scientists with experience in infectious diseases, virology, clinical trials and vaccine epidemiology have been invested in presenting this summary of the evidence. Large registry-based studies have identified plausible associations between HPV vaccination and autoimmune conditions, including premature ovarian insufficiency or premature ovarian failure, Guillain-Barré syndrome (GBS), postural orthostatic tachycardia syndrome and chronic regional pain syndrome. While it is easy to be enthusiastic about recent advances in human vaccine technology, we should keep in mind that achieving real and lasting good health is much more than just the absence of a certain virus. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now What is HPV? According to the CDC, HPV is the most common sexually transmitted infection in the U.S. HPV is a small DNA virus infecting human cutaneous epithelial cells in the mucosa and skin. More than 150 strains of the HPV virus have been identified. HPV infection is so common that the majority of sexually active people will get it at some point in their lives, even if they have only one or very few sexual partners. It can spread through sexual intercourse and oral sex. It can also pass between people through skin-to-skin contact, even by people who have no symptoms. HPV infection causes genital warts, some of which can turn into cancer. For the most part, however, HPV infection is benign. More than 90% of HPV infections cause no clinical symptoms and are self-limited, meaning the virus is cleared by the body via natural immunological defenses. HPV-associated cancers High-risk HPV types (types 16, 18 and others) can cause cervical cell abnormalities that are precursors to cancers. Type 16 is associated with approximately 50% of cervical cancers worldwide, and types 16 and 18 together are linked to 66% of cervical cancers. An additional five high-risk types, 31, 33, 45, 52 and 58, are linked with another 15% of cervical cancers and 11% of all HPV-associated cancers. Infection with a high-risk HPV type is associated with a higher chance of the development of cervical cancer but, by itself, HPV infection is not the sole risk factor to cause cancer. There are many other reasons, as discussed in this paper. Given the prevalence of infection, it is unsurprising that globally, cervical cancer is the fourth most common cancer in women. In 2018, an estimated 570,000 women were diagnosed with cervical cancer worldwide and more than 300,000 died of the disease. In the U.S., nearly 50,000 new HPV-associated cancers occur annually, with women infected at a slightly higher rate than men. But in 9 out of 10 cases, HPV goes away within two years without causing health problems. Only persistent HPV infections may lead to cancer. These infections evade the immune system’s innate cell-mediated defenses. The incidence of cervical cancer can be controlled as a result of the implementation of routine testing and screening, including Pap and DNA tests. HPV vaccines Three HPV vaccines — bivalent HPV vaccine (Cervarix, 2vHPV), quadrivalent HPV vaccine (Gardasil, 4vHPV or HPV4) and 9-valent HPV vaccine (Gardasil 9, 9vHPV) — have been licensed by the FDA. The HPV vaccine uses recombinant technology to assemble the shell of the virus — L1 capsid protein. These viral-like particles do not contain the virus genome and are not infectious. Cervarix, developed by GlaxoSmithKline, is a bivalent vaccine against HPV types 16 and 18, that was pulled from the U.S. market in 2016 due to “very low market demand.” Merck’s original Gardasil vaccine was designed to prevent infections from four strains (types 6, 11, 16 and 18). On June 8, 2006, after the FDA’s fast-tracked review, Gardasil was approved for use in females ages 9 to 26 for the prevention of cervical, vulvar and vaginal cancers. According to the label accompanying the vaccine, the ingredients in Merck’s first Gardasil vaccine were proteins of HPV, amorphous aluminum hydroxyphosphate sulfate, yeast protein, sodium chloride, L-histidine, polysorbate 80, sodium borate and water for injection. On Oct. 16, 2009, the FDA approved Gardasil (HPV4) for use in boys ages 9 through 26 for the prevention of genital warts caused by HPV types 6 and 11, but not for cancer. In 2010, it approved Gardasil for the prevention of anal cancer in males and females ages 9 to 26. Four years later, the FDA approved an updated vaccine, Merck’s Gardasil 9, for use in girls ages 9 to 26 and boys ages 9 to 15 for the prevention of cervical, vaginal and anal cancers. Gardasil 9 contains the same ingredients as Gardasil, but offers protection against nine HPV strains, adding five additional types (HPV types 31, 33, 45, 52 and 58). The current HPV vaccination schedule recommended by the CDC is two doses for both boys and girls aged 11 or 12. However, it is approved for children as young as 9. The second dose is given 6 to 12 months after the first. For those aged 15 and above, a three-dose schedule is implemented at one- to two-month and six-month intervals, although antibody-level studies suggest that two doses are sufficient. The vaccine prompts the body to produce neutralizing antibodies against HPV. Antibody responses appear to peak seven months after the first dose (or one month after the third dose). The vaccine-induced antibody levels appear to be 10 to 100 times higher than those after natural infection. The high vaccine effectiveness (90 to 98%) against the fast-growing, abnormal cells which may cause precancerous lesions in people ages 16 to 26 suggested that the best timing for vaccination was to give it to patients before they became sexually active. HPV VAERS reports from 2 large countries U.S. HPV vaccine adverse events On Aug. 19, 2009, the Journal of the American Medical Association published an article authored by scientists from the FDA and CDC that reviewed the safety data for Gardasil for adverse events reported to VAERS between June 2006 through December 2008. During that time, there were 12,424 reports of adverse events. Of these, 772 (6.2%) were serious. VAERS is a passive surveillance system, which is subject to multiple limitations, including underreporting, unconfirmed diagnosis, lack of denominator data and no unbiased comparison groups. Nevertheless, it is a useful and important tool for detecting postmarket safety issues with vaccines. A disproportionately high percentage of Gardasil VAERS reports were of syncope (fainting) and venous thromboembolic events (blood clots in the veins) compared with other vaccines. There were 8.2 syncope events per 100,000 HPV doses and 0.2 venous thromboembolic events per 100,000 HPV doses reported, respectively. The Gardasil package insert includes a warning about fainting, fever, dizziness, nausea and headaches (page 1) and notes at least the following adverse reactions reported during postmarketing surveillance (section 6.2): Guillain-Barré syndrome, transverse myelitis, motor neuron disease, venous thromboembolic events, pancreatitis and autoimmune disorders. Australia HPV vaccines adverse events In 2007, Australia reported an annual adverse drug reaction rate of 7.3/100,000, the highest since 2003, representing an 85% increase from 2006. Per the analysis of the Adverse Drug Reactions System database by the Australian Department of Health and Aging, this increase was “almost entirely due to” reports following the national rollout of the three-dose HPV vaccination program for young females in April 2007; 705 of the 1,538 adverse drug reactions reported that year were from the Gardasil vaccine. 1 vaccine adverse events australia chart In Australia, the ADR increase in 2007 was almost entirely due to the three-dose HPV vaccination program for females aged 12 to 26 years in April 2007. Credit: Australian Government Department of Health and Aged Care. Moreover, though people may take different vaccines other than HPV, the HPV vaccine was the only suspected vaccine to cause adverse reactions in 96% of records. Twenty-nine percent had causality ratings of “certain” or “probable” and 6% were defined as “serious.” 2 vaccine types vaccine suspected chart In these HPV-induced ADRs, 674 were suspected to be related to HPV vaccines, 203 had causality ratings of “certain” or “probable,” and 43 were defined as “serious.” Credit: Australian Government Department of Health and Aged Care. Japan withdraws recommendation, vaccine acceptance plunged In 2013, the Japanese raised concerns about a variety of widely reported post-vaccination serious adverse events. This led the government to suspend recommending the HPV vaccine for six years. Vaccine acceptance of HPV in Japan plunged significantly after 2013, from 42.9% to 14.3%, or from 65.4% to 3.9%. Researchers around the world also started to investigate HPV safety. A World Health Organization (WHO) position paper released on July 14, 2017, concluded that the HPV vaccines were “extremely safe.” The same report estimated approximately 1.7 cases of anaphylaxis per million HPV doses, that no association with GBS was found, and that syncope (fainting) was “established as a common anxiety or stress-related reaction to the injection.” In the spring of 2022, Japan announced it was relaunching its HPV vaccination drive. Mainstream news outlets reported that for thousands of women, the cost of caution may have led to preventable HPV-induced cancers and an estimated 5,000 to 5,700 deaths. However, a true risk-benefit analysis would also consider the number of serious adverse events prevented by putting the program on hold. The question remains: Was Japan’s caution warranted, or should their national vaccination program have continued? Ovarian insufficiency Concerns that the vaccine may be negatively affecting fertility have been detailed in the scientific literature. In 2014, a peer-reviewed case series describing premature ovarian failure among Australian women following HPV vaccination was published in the Journal of Investigative Medicine. This prompted other researchers to systematically examine the VAERS data to see if there was a connection between premature ovarian failure and Gardasil. Their study found a “potential safety signal” and concluded that “further investigations are warranted.” VAERS analysis on ovarian failure Two recent publications based on VAERS reports (first study, second study) found that events with a probable autoimmune background were significantly more frequent after HPV vaccination compared to other vaccinations. The team of international scientists that did the second study evaluated reports between 1990 and 2018. They found that among the 228,341 premature ovarian failure reports, 0.1% was considered to be associated with HPV vaccination with a median age of 15 years and the time to onset was 20.5 days following vaccination. The primary symptoms were amenorrhea (80.4%) and premature menopause (15.3%). Most strikingly, the mean number of premature ovarian failure cases increased significantly from 1.4 per year prior to 2006 to 22.2 per year after the HPV vaccine was approved, with a proportional reporting ratio of 46. The investigators noted that the WHO and CDC declared the HPV vaccine safe regardless of lacking adequate research into safety concerns. For example, the authors note that in a CDC-sponsored VAERS study, 17 cases of premature ovarian failure were identified but 15 were excluded due to insufficient information to confirm the diagnosis. A separate observational study using the Vaccine Safety Datalink found no increased risk. But this study was too underpowered to detect a signal. In addition, a cross-sectional survey study using National Health and Nutrition Examination Survey data relied on an inaccurate measurement of premature ovarian failure and self-reported HPV vaccination. In summary, the researchers detected a strong safety signal even after accounting for a potential upswing in reports due to media coverage after the product launch (they refer to this as “notoriety bias”). Because VAERS is a passive reporting system, the data may be incomplete and are often unconfirmed by physicians. Therefore, this study cannot provide a definitive link between HPV vaccination and premature ovarian insufficiency or premature ovarian failure but does generate a hypothetical link. The authors of the second study conclude by insisting that “this signal warrants well-designed and appropriate epidemiological research.” They note that “if the signal is confirmed, the risk is small compared to the lifetime risk of cervical cancer.” However, the benefit-risk profile on an individual level is not uniform. Given the health impacts of premature ovarian insufficiency and premature ovarian failure — some of which may be irreversible — and the declining mortality rate for cervical cancer even in the prevaccine era, the risk-benefit profile for HPV vaccination remains unclear. 3 case reports on ovarian insufficiency In the 2014 investigation mentioned above, a general practitioner in Australia noticed that three girls developed premature ovarian insufficiency following HPV4 vaccination. As a result of vaccination, each of the girls (ages 16, 16 and 18) had been prescribed oral contraception to treat menstrual cycle irregularities. Typically, women present with amenorrhea (no periods) or oligomenorrhea (infrequent periods) as the initial symptom of premature ovarian insufficiency. One girl had irregular periods following three doses of HPV vaccination. She then became amenorrheic and was diagnosed with premature ovarian insufficiency. Another girl’s periods were “like clockwork” until after the third HPV dose, which she received at age 15. Her first cycle after being vaccinated for the third time started two weeks late, and her next cycle was two months late. The final cycle began nine months later. The patient had no family history of early menopause. She was diagnosed with premature ovarian failure at 16. Lab work found hormone levels consistent with those of postmenopausal women, but her bone mineral density was normal. The authors of this case series noted that in preclinical studies of HPV4, the five-week-old rats only conceived one litter and the only available toxicology studies appear to be on the male rodent reproductive system. However, only two of three doses were administered prior to mating, and the overall fecundity was 95%, slightly lower than the control rats (98%) that received no vaccination prior to mating. The dose tolerance recommendations were based on an average weight of 50 kilograms for an adolescent girl but failed to take into account that HPV4 is administered to girls ages 9 to 13 years, who range in weight from 28 to 46 kilograms. Danish retrospective cohort study finds no link A 2021 study also evaluated premature ovarian insufficiency in a nationwide cohort of nearly 1 million Danish females ages 11 to 34 years. The researchers used Cox proportional hazard regression to detect an increased risk of premature ovarian insufficiency diagnosis by HPV4 vaccination status during the years 2007-2016. The hazard ratio for premature ovarian insufficiency (vaccinated versus unvaccinated) was 0.96. One limitation was that data on age at menarche (first menstruation) and oral contraceptive use were not available. Girls who had not yet reached menarche would not be at risk for premature ovarian insufficiency, of course. The authors excluded girls under age 15 in a sensitivity analysis and still found no signal, concluding that no association was found between HPV4 vaccination and premature ovarian insufficiency. Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases from China, is the chief scientific officer and co-founder of a Swiss biotech company and a former senior medical scientific expert for antiviral drug development at Novartis Pharma in Switzerland. If you or your child suffered harm after receiving the Gardasil HPV vaccine, you may have a legal claim. Please visit Wisner Baum for a free case evaluation. Click here to watch a Gardasil litigation update interview with Wisner Baum Senior Partner Bijan Esfandiari. The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children's Health Defense. https://childrenshealthdefense.org/defender/hpv-vaccine-safety-concerns-part-1-et/ https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-1.html
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    The Truth About HPV Vaccination, Part 1: How Safe Is It, Really?
    This first installment in a multi-part series about the human papillomavirus, or HPV, vaccine explores peer-reviewed scientific literature that reveals serious safety concerns about a vaccine widely regarded as safe.
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    The Truth About HPV Vaccination, Part 1: How Safe Is It, Really?
    This first installment in a multi-part series about the human papillomavirus, or HPV, vaccine explores peer-reviewed scientific literature that reveals serious safety concerns about a vaccine widely regarded as safe.
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  • Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule
    A review paper published last week in the journal Cureus is the first peer-reviewed paper to call for a global moratorium on the COVID-19 mRNA vaccines. The authors say that reanalyzed data from the vaccine makers’ trials and high rates of serious post-injection injuries indicate the mRNA gene therapy vaccines should not have been authorized for use.

    Brenda Baletti, Ph.D.
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    Governments should endorse a global moratorium on mRNA vaccines until all questions about their safety have been thoroughly investigated, according to the authors of a new, peer-reviewed article on the COVID-19 vaccine trials and the global vaccination campaign published last week in Cureus, Journal of Medical Science.

    Cureus is a web-based peer-reviewed open-access general medical journal using prepublication peer review.

    The authors surveyed published research on the pharmaceutical companies’ vaccine trials and related adverse events. They also called for the COVID-19 vaccines to be removed immediately from the childhood immunization schedule.

    After the first reports from vaccine trials claimed they were 95% effective in preventing COVID-19, serious problems with method, execution and reporting in the trials became public, which the paper reviewed in detail.

    Evidence also shows the products never underwent adequate safety and toxicological testing, and since the vaccine rollout, researchers have identified a significant number of adverse events (AEs) and serious adverse events (SAEs).

    Authors M. Nathaniel Mead, Stephanie Seneff, Ph.D., Russ Wolfinger, Ph.D., Jessica Rose, Ph.D., Kris Denhaerynck, Ph.D., Steve Kirsch and Dr. Peter McCullough detailed the vaccines’ potential serious harms to humans, vaccine control and processing issues, the mechanisms behind AEs, the immunological reasons for vaccine inefficacy and the mortality data from the registrational trials.

    They concluded, “Federal agency approval of the COVID-19 mRNA injectable products on a blanket-coverage population-wide basis had no support from an honest assessment of all relevant registrational data and commensurate consideration of risks versus benefits.”

    They also called for the vaccines to be immediately removed from the childhood immunization schedule and for the suspension of the boosters.

    “It is unethical and unconscionable to administer an experimental vaccine to a child who has a near-zero risk of dying from COVID-19 (IFR, 0.0003%) but a well-established 2.2% risk of permanent heart damage based on the best prospective data available,” they wrote.

    Finally, the authors called for a full investigation into misconduct by the pharmaceutical companies and the regulatory agencies.

    It is the first peer-reviewed study to call for a moratorium on the COVID-19 mRNA products, Rose told The Defender.

    “Once a proper assessment of the safety and efficacy claims was made herein — upon which the emergency use authorization (EUA)’s and ultimate final authorizations were granted — it was found that the COVID-19 injectable products were neither safe nor effective,” she added.

    According to McCollough, “mRNA should never have been authorized for human use.”

    Lead author Mead told The Defender, “Our view is that any risk-benefit analysis must consider how much the presumed benefit in terms of reduced COVID-19 related mortality is offset by the potential increase in vaccine-induced mortality.”

    Here are six takeaways from the review:

    1. The COVID-19 ‘vaccines’ are reclassified gene therapies that were rushed through the regulatory process in a historically unprecedented manner

    Before the seven-month authorization process for the mRNA vaccines, no vaccine had ever gone to market without undergoing testing of at least four years, with typical timelines averaging 10 years.

    To speed the process, the companies skipped preclinical studies of potential toxicity from multiple doses and cut the typical 6-12 month observation period for identifying longer-term adverse effects and the established 10-15-year period for monitoring for long-term effects such as cancer and autoimmune disorders, the authors wrote.

    The trials prioritized documenting effective symptom reduction over SAE and mortality. This was particularly concerning, the authors argued, because mRNA products are gene therapy products reclassified as vaccines and then given EUA for the first time ever for use against a viral disease.

    However, the gene therapies’ components have not been thoroughly evaluated for safety for use as vaccines.

    There is an uninvestigated and major concern that the mRNA could transform body cells into viral protein factories — with no off-switch — that produce the spike protein for a prolonged period causing chronic systemic inflammation and immune dysfunction.

    The spike protein in the vaccine, the authors said, is associated with more severe immunopathology and other AEs than the spike protein in the virus itself.

    The authors suggested that massive government investment in mRNA technology, including hundreds of millions before the pandemic and tens of billions once it began, meant, “U.S. federal agencies were strongly biased toward successful outcomes for the registrational trials.”

    The financial incentives along with political pressures to deliver a rapid solution likely influenced a series of flawed decisions that compromised the integrity of the trials and downplayed serious scientific concerns about risks with the technology, they added.

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    2. Steps were taken in trials to overestimate vaccine efficacy

    Because the trials were designed to assess whether the mRNA vaccine reduced symptoms, they did not measure whether the vaccines prevented severe disease and death. Yet the vaccine makers repeatedly claimed that they do.

    “No large randomized double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalization, or death,” the authors wrote.

    Additionally, the number of people who contracted clinical COVID-19 in both the placebo and intervention groups was “too small to draw meaningful, pragmatic, or broad-sweeping conclusions with regard to COVID-19 morbidity and mortality.”

    Pfizer’s 95 % efficacy claims were based on 162 of 22,000 placebo recipients contracting PCR-confirmed COVID-19 compared to eight of 22,000 in the vaccine group. None of the placebo recipients died from COVID-19. In the Moderna trials, only one placebo death was attributed to COVID-19.

    There was also a much larger percentage of “suspected COVID-19 cases” in both groups, with participants showing COVID-19 symptoms but a negative PCR test. When factoring in those cases, measures of vaccine efficacy drop to about 19%.

    The trial subject pool was comprised of largely young and healthy individuals, excluding key groups — children, pregnant women, elderly and immunocompromised people — which can also obscure the vaccine’s actual efficacy and safety.

    Findings from reanalyses of data from the Pfizer trials can be interpreted as showing the vaccines made “no significant difference” in reducing all-cause mortality in the vaccinated versus unvaccinated groups at 20 weeks into the trial, the authors wrote.

    Even the six-month post-marketing data Pfizer presented to the U.S. Food and Drug Administration (FDA) showed no reduction in all-cause mortality from the vaccine.

    The authors reanalyzed that data, adjusting the analysis of deaths to better account for the fact that when Pfizer unblinded the study people from the placebo group took the vaccine, and found the vaccine group had a higher mortality rate (0.105%) than the unvaccinated group (0.0799%), which they said was a conservative estimate.

    One of the most glaring issues with the registrational trials, they noted, was that they exclusively focused on measuring risk reduction — the ratio of COVID-19 symptom rates in the vaccine group versus the placebo group — rather than measuring absolute risk reduction, which is the likelihood someone will show COVID-19 symptoms relative to people in the population at large.

    According to FDA guidelines, accounting for both approaches is crucial to avoid the misguided use of pharmaceutical products — but the data were omitted, leading to an overestimation of an intervention’s clinical utility.

    While both vaccines touted an approximately 95% risk reduction figure as their efficacy figure, the absolute risk reductions for Pfizer and Moderna’s vaccines were 0.7% and 1.1% respectively.

    “A substantial number of individuals would need to be injected in order to prevent a single mild-to-moderate case of COVID-19,” the authors wrote.

    As an example, using a conservative estimate that 119 people would need to be vaccinated to prevent infection, and assuming that COVID-19 had a 0.23% infection fatality rate, they wrote that approximately 52,000 vaccinations would be necessary to prevent a single COVID-19-related death.

    However, “Given trial misconduct and data integrity problems … the true benefit is likely to be much lower,” they wrote.

    And, they added, one would need to assess that benefit along with harms, which they estimate to be 27 deaths per 100,000 doses of Pfizer. That means, using the most conservative estimates, “for every life saved, there were 14 times more deaths caused by the modified mRNA injections.”

    They also noted that post-rollout evidence confirmed the efficacy claims were overstated. For example, two large cohort Cleveland clinic studies showed the vaccine could not confer protection against COVID-19 — instead, in those trials, more vaccinated people were more likely to contract COVID-19.

    One study showed the risk of “breakthrough” infection was significantly higher among people who were boosted and that more vaccinations resulted in a greater risk of COVID-19.

    A second study showed adults who were not “up-to-date” with their shots had a 23% lower incidence of COVID-19 than their “up-to-date” colleagues.

    3. The trials underestimated the adverse events, including death, despite evidence in the data.

    Harms were also underreported and underestimated for a number of reasons, according to the authors, a practice that tends to be common in randomized industry-sponsored vaccine trials in general and “exceptionally evident” here.

    First, because Pfizer unblinded the trial within just a few weeks of the emergency use authorization and allowed people in the placebo group to take the vaccine, there was not sufficient time to identify late-occurring harms because there was no longer a control group.

    “Was this necessary, given that none of the deaths in the Pfizer trial were attributed to COVID-19 as the primary cause, and given the very low IFR [infection fatality rate] for a relatively healthy population?” they asked.

    Also, trial coordinators were “haphazard” in their approach to monitoring AEs. They prioritized documenting events thought to be related to COVID-19 rather than to the vaccines for the first seven days and only recorded “unsolicited” AEs for 30-60 days. After that period, even very SAEs, like death, were not recorded. Even for the AEs recorded in the first seven days, they only solicited data from 20% of the population.

    None of the trial data was independently verified. “Such secrecy may have enabled the industry to more easily present an inflated and distorted estimate of the genetic injections’ benefits, along with a gross underestimation of potential harms,” they wrote.

    Subsequent analysis by Michels et al. revealed that deaths and other SAEs — like life-threatening conditions, inpatient hospitalization or extension of hospitalization, persistent or significant disability/incapacity, a congenital anomaly, or a medically significant event — did occur after the cutoff period and before the FDA advisory meeting where emergency authorization was recommended.

    During the first 33 weeks of the Pfizer trials, 38 subjects died, according to Pfizer’s own data, although independent research by Michels et al. estimated that that number is only approximately 17% of the actual projected number due to missing data.

    And after that, the rate of deaths continued to increase. Michaels et al. found Pfizer failed to report a substantial increase in the number of deaths due to cardiovascular events. They also found a consistent pattern of reporting delays on the date of the death on subjects’ case reports.

    Overall, the review authors reported that there were “twice as many cardiac deaths proportionately among vaccinated compared to unvaccinated subjects in the Pfizer trials.”

    In their discussion, the authors wrote “Based on the extended Pfizer trial findings, our person-years estimate yielded a 31% increase in overall mortality among vaccine recipients, a clear trend in the wrong direction.”

    This raises serious red flags about how the registrational trials were conducted, Mead said. “Assessments of the safety profile of the COVID-19 modified mRNA injections warrant an objective precautionary perspective, any substantial upward trend in all cause mortality within the intervention arm of the trial population reflects badly on the intervention.”

    4. Numbers of SAEs in the trials and post-rollout reporting are well-documented, despite claims to the contrary.

    Both Pfizer and Moderna found about 125 SAEs per 100,000 vaccine recipients, or one SAE for every 800 vaccines. However, because the trials excluded more vulnerable people, the authors note, even higher proportions of SAEs would be expected in the general population.

    The Fraiman et al. reanalysis of the Pfizer trial data found a significant 36% higher risk of SAEs, which included deaths and many life-threatening conditions in the vaccinated participants.

    Official SAEs for other vaccines average around only 1-2 per million. Fraiman et alestimated 1,250 SEAs per million vaccines, exceeding that benchmark by “at least 600-fold.”

    After the vaccine rollout, analyses of two large drug safety reporting systems in the U.S. and Europe identified signals for myocardial infarction, pulmonary embolism, cardio-respiratory arrest, cerebral infarction, and cerebral hemorrhage associated with both mRNA vaccines, along with ischemic stroke.

    And millions of AEs have been reported to those systems.

    Another study by Skidmore et al. estimated the total number of fatalities from the vaccines in 2021 alone was 289,789. Autopsy studies have also provided additional evidence of serious harms, including evidence that most COVID-19 mRNA vaccine-related deaths resulted from injury to the cardiovascular system.

    In multiple autopsy studies, German pathologist Aren Burkhardt documented the presence of vaccine-mRNA-produced spike proteins in blood vessel walls and brain tissues. This research helps to explain documented vaccine-induced toxicities affecting the nervous, immune, reproductive and other systems.

    The Pfizer data also showed an overwhelming number of adverse effects. According to a confidential document released in August 2022, Pfizer had documented approximately 1.6 million AEs affecting nearly every organ system, and one-third of them were classified as serious.

    In Pfizer’s trial, Michels and colleagues found a nearly 4-fold increase (OR 3.7, 95%CI 1.02-13.2, p = 0.03) in serious cardiac events (e.g., heart attack, acute coronary syndrome) in the vaccine group. Neither the original trial report nor Pfizer’s Summary Clinical Safety report acknowledged or commented on this safety signal.

    “The serious adverse events are all well documented,” Mead said. “Yet it’s surprising to see so many in the medical field continue to ignore or dismiss outright the latter half of the equation when considering all cause mortality trends.”

    5. The failure to appropriately test for safety and toxicity poses serious problems.

    Researchers have raised concerns that the mRNA technology is inherently unstable and difficult to store, which leads to batch variability and contamination linked to different rates of AEs.

    Recent findings by McKernan et al. that found Pfizers’ mRNA vaccines are contaminated with plasmid DNA that shouldn’t be present — and wasn’t present in the vaccines used in the trials – raising serious safety issues.

    That’s because “Process 1,” used in the trials to generate the vaccines involved in vitro transcription of synthetic DNA — essentially a “clean” process. However, that process isn’t viable for mass production, so the manufacturers used “Process 2,” which involves using E. coli bacteria to replicate the plasmids.

    Removing plasmids E coli. can result in residual plasmids in the vaccines and the effects of their presence is unknown.

    McKernan’s work also revealed the presence of DNA from simian virus 40 (SV40), an oncogenic DNA virus originally isolated in 1960 from contaminated polio vaccines, induces lymphomas, brain tumors, and other malignancies in laboratory animals, raising other safety concerns.

    Researchers from Cambridge published a paper in Nature in December 2023, where they found an inherent defect in the modified RNA instructions for the spike protein in COVID-19 immunizations that causes the machinery that translates the gene to the spike protein to “slip” about 10% of the time

    This process creates “frameshifts” that cause cells to produce “off-target” proteins in addition to the spike. These proteins, which developers either failed to look for or did not report to regulators, cause undesirable immune responses whose long-term effects are unknown.

    6. There are many different possible biological mechanisms that cause AEs and vaccine ineffectiveness.

    The review points readers to a series of papers that explain a number of different theories to explain the high number of AEs from the COVID-19 mRNA vaccines.

    “The mechanisms of molecular mimicry, antigen cross-reactivity, pathogenic priming, viral reactivation, immune exhaustion, and other factors related to immune dysfunction all reinforce the biological plausibility for vaccine-induced pathogenesis of malignant and autoimmune diseases,” they wrote. And these mechanisms of immune activation are distinct from the body’s response to a viral infection.

    They also note the toxic effects of the primary adjuvant, PEG, and of the spike protein itself.

    They close their analysis of the vaccines with a complex explanation for the different immunological basis for protection provided by the vaccines versus natural immunity through infection. They explain the mechanisms for vaccine failure and problems generated by the ability for the mRNA vaccines to perpetuate the emergence of new variants.

    https://childrenshealthdefense.org/defender/scientists-global-moratorium-mrna-vaccines-removal-childhood-schedule/


    https://donshafi911.blogspot.com/2024/01/scientists-call-for-global-moratorium.html
    Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule A review paper published last week in the journal Cureus is the first peer-reviewed paper to call for a global moratorium on the COVID-19 mRNA vaccines. The authors say that reanalyzed data from the vaccine makers’ trials and high rates of serious post-injection injuries indicate the mRNA gene therapy vaccines should not have been authorized for use. Brenda Baletti, Ph.D. global moratorium mrna covid vaccine feature Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. Governments should endorse a global moratorium on mRNA vaccines until all questions about their safety have been thoroughly investigated, according to the authors of a new, peer-reviewed article on the COVID-19 vaccine trials and the global vaccination campaign published last week in Cureus, Journal of Medical Science. Cureus is a web-based peer-reviewed open-access general medical journal using prepublication peer review. The authors surveyed published research on the pharmaceutical companies’ vaccine trials and related adverse events. They also called for the COVID-19 vaccines to be removed immediately from the childhood immunization schedule. After the first reports from vaccine trials claimed they were 95% effective in preventing COVID-19, serious problems with method, execution and reporting in the trials became public, which the paper reviewed in detail. Evidence also shows the products never underwent adequate safety and toxicological testing, and since the vaccine rollout, researchers have identified a significant number of adverse events (AEs) and serious adverse events (SAEs). Authors M. Nathaniel Mead, Stephanie Seneff, Ph.D., Russ Wolfinger, Ph.D., Jessica Rose, Ph.D., Kris Denhaerynck, Ph.D., Steve Kirsch and Dr. Peter McCullough detailed the vaccines’ potential serious harms to humans, vaccine control and processing issues, the mechanisms behind AEs, the immunological reasons for vaccine inefficacy and the mortality data from the registrational trials. They concluded, “Federal agency approval of the COVID-19 mRNA injectable products on a blanket-coverage population-wide basis had no support from an honest assessment of all relevant registrational data and commensurate consideration of risks versus benefits.” They also called for the vaccines to be immediately removed from the childhood immunization schedule and for the suspension of the boosters. “It is unethical and unconscionable to administer an experimental vaccine to a child who has a near-zero risk of dying from COVID-19 (IFR, 0.0003%) but a well-established 2.2% risk of permanent heart damage based on the best prospective data available,” they wrote. Finally, the authors called for a full investigation into misconduct by the pharmaceutical companies and the regulatory agencies. It is the first peer-reviewed study to call for a moratorium on the COVID-19 mRNA products, Rose told The Defender. “Once a proper assessment of the safety and efficacy claims was made herein — upon which the emergency use authorization (EUA)’s and ultimate final authorizations were granted — it was found that the COVID-19 injectable products were neither safe nor effective,” she added. According to McCollough, “mRNA should never have been authorized for human use.” Lead author Mead told The Defender, “Our view is that any risk-benefit analysis must consider how much the presumed benefit in terms of reduced COVID-19 related mortality is offset by the potential increase in vaccine-induced mortality.” Here are six takeaways from the review: 1. The COVID-19 ‘vaccines’ are reclassified gene therapies that were rushed through the regulatory process in a historically unprecedented manner Before the seven-month authorization process for the mRNA vaccines, no vaccine had ever gone to market without undergoing testing of at least four years, with typical timelines averaging 10 years. To speed the process, the companies skipped preclinical studies of potential toxicity from multiple doses and cut the typical 6-12 month observation period for identifying longer-term adverse effects and the established 10-15-year period for monitoring for long-term effects such as cancer and autoimmune disorders, the authors wrote. The trials prioritized documenting effective symptom reduction over SAE and mortality. This was particularly concerning, the authors argued, because mRNA products are gene therapy products reclassified as vaccines and then given EUA for the first time ever for use against a viral disease. However, the gene therapies’ components have not been thoroughly evaluated for safety for use as vaccines. There is an uninvestigated and major concern that the mRNA could transform body cells into viral protein factories — with no off-switch — that produce the spike protein for a prolonged period causing chronic systemic inflammation and immune dysfunction. The spike protein in the vaccine, the authors said, is associated with more severe immunopathology and other AEs than the spike protein in the virus itself. The authors suggested that massive government investment in mRNA technology, including hundreds of millions before the pandemic and tens of billions once it began, meant, “U.S. federal agencies were strongly biased toward successful outcomes for the registrational trials.” The financial incentives along with political pressures to deliver a rapid solution likely influenced a series of flawed decisions that compromised the integrity of the trials and downplayed serious scientific concerns about risks with the technology, they added. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now 2. Steps were taken in trials to overestimate vaccine efficacy Because the trials were designed to assess whether the mRNA vaccine reduced symptoms, they did not measure whether the vaccines prevented severe disease and death. Yet the vaccine makers repeatedly claimed that they do. “No large randomized double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalization, or death,” the authors wrote. Additionally, the number of people who contracted clinical COVID-19 in both the placebo and intervention groups was “too small to draw meaningful, pragmatic, or broad-sweeping conclusions with regard to COVID-19 morbidity and mortality.” Pfizer’s 95 % efficacy claims were based on 162 of 22,000 placebo recipients contracting PCR-confirmed COVID-19 compared to eight of 22,000 in the vaccine group. None of the placebo recipients died from COVID-19. In the Moderna trials, only one placebo death was attributed to COVID-19. There was also a much larger percentage of “suspected COVID-19 cases” in both groups, with participants showing COVID-19 symptoms but a negative PCR test. When factoring in those cases, measures of vaccine efficacy drop to about 19%. The trial subject pool was comprised of largely young and healthy individuals, excluding key groups — children, pregnant women, elderly and immunocompromised people — which can also obscure the vaccine’s actual efficacy and safety. Findings from reanalyses of data from the Pfizer trials can be interpreted as showing the vaccines made “no significant difference” in reducing all-cause mortality in the vaccinated versus unvaccinated groups at 20 weeks into the trial, the authors wrote. Even the six-month post-marketing data Pfizer presented to the U.S. Food and Drug Administration (FDA) showed no reduction in all-cause mortality from the vaccine. The authors reanalyzed that data, adjusting the analysis of deaths to better account for the fact that when Pfizer unblinded the study people from the placebo group took the vaccine, and found the vaccine group had a higher mortality rate (0.105%) than the unvaccinated group (0.0799%), which they said was a conservative estimate. One of the most glaring issues with the registrational trials, they noted, was that they exclusively focused on measuring risk reduction — the ratio of COVID-19 symptom rates in the vaccine group versus the placebo group — rather than measuring absolute risk reduction, which is the likelihood someone will show COVID-19 symptoms relative to people in the population at large. According to FDA guidelines, accounting for both approaches is crucial to avoid the misguided use of pharmaceutical products — but the data were omitted, leading to an overestimation of an intervention’s clinical utility. While both vaccines touted an approximately 95% risk reduction figure as their efficacy figure, the absolute risk reductions for Pfizer and Moderna’s vaccines were 0.7% and 1.1% respectively. “A substantial number of individuals would need to be injected in order to prevent a single mild-to-moderate case of COVID-19,” the authors wrote. As an example, using a conservative estimate that 119 people would need to be vaccinated to prevent infection, and assuming that COVID-19 had a 0.23% infection fatality rate, they wrote that approximately 52,000 vaccinations would be necessary to prevent a single COVID-19-related death. However, “Given trial misconduct and data integrity problems … the true benefit is likely to be much lower,” they wrote. And, they added, one would need to assess that benefit along with harms, which they estimate to be 27 deaths per 100,000 doses of Pfizer. That means, using the most conservative estimates, “for every life saved, there were 14 times more deaths caused by the modified mRNA injections.” They also noted that post-rollout evidence confirmed the efficacy claims were overstated. For example, two large cohort Cleveland clinic studies showed the vaccine could not confer protection against COVID-19 — instead, in those trials, more vaccinated people were more likely to contract COVID-19. One study showed the risk of “breakthrough” infection was significantly higher among people who were boosted and that more vaccinations resulted in a greater risk of COVID-19. A second study showed adults who were not “up-to-date” with their shots had a 23% lower incidence of COVID-19 than their “up-to-date” colleagues. 3. The trials underestimated the adverse events, including death, despite evidence in the data. Harms were also underreported and underestimated for a number of reasons, according to the authors, a practice that tends to be common in randomized industry-sponsored vaccine trials in general and “exceptionally evident” here. First, because Pfizer unblinded the trial within just a few weeks of the emergency use authorization and allowed people in the placebo group to take the vaccine, there was not sufficient time to identify late-occurring harms because there was no longer a control group. “Was this necessary, given that none of the deaths in the Pfizer trial were attributed to COVID-19 as the primary cause, and given the very low IFR [infection fatality rate] for a relatively healthy population?” they asked. Also, trial coordinators were “haphazard” in their approach to monitoring AEs. They prioritized documenting events thought to be related to COVID-19 rather than to the vaccines for the first seven days and only recorded “unsolicited” AEs for 30-60 days. After that period, even very SAEs, like death, were not recorded. Even for the AEs recorded in the first seven days, they only solicited data from 20% of the population. None of the trial data was independently verified. “Such secrecy may have enabled the industry to more easily present an inflated and distorted estimate of the genetic injections’ benefits, along with a gross underestimation of potential harms,” they wrote. Subsequent analysis by Michels et al. revealed that deaths and other SAEs — like life-threatening conditions, inpatient hospitalization or extension of hospitalization, persistent or significant disability/incapacity, a congenital anomaly, or a medically significant event — did occur after the cutoff period and before the FDA advisory meeting where emergency authorization was recommended. During the first 33 weeks of the Pfizer trials, 38 subjects died, according to Pfizer’s own data, although independent research by Michels et al. estimated that that number is only approximately 17% of the actual projected number due to missing data. And after that, the rate of deaths continued to increase. Michaels et al. found Pfizer failed to report a substantial increase in the number of deaths due to cardiovascular events. They also found a consistent pattern of reporting delays on the date of the death on subjects’ case reports. Overall, the review authors reported that there were “twice as many cardiac deaths proportionately among vaccinated compared to unvaccinated subjects in the Pfizer trials.” In their discussion, the authors wrote “Based on the extended Pfizer trial findings, our person-years estimate yielded a 31% increase in overall mortality among vaccine recipients, a clear trend in the wrong direction.” This raises serious red flags about how the registrational trials were conducted, Mead said. “Assessments of the safety profile of the COVID-19 modified mRNA injections warrant an objective precautionary perspective, any substantial upward trend in all cause mortality within the intervention arm of the trial population reflects badly on the intervention.” 4. Numbers of SAEs in the trials and post-rollout reporting are well-documented, despite claims to the contrary. Both Pfizer and Moderna found about 125 SAEs per 100,000 vaccine recipients, or one SAE for every 800 vaccines. However, because the trials excluded more vulnerable people, the authors note, even higher proportions of SAEs would be expected in the general population. The Fraiman et al. reanalysis of the Pfizer trial data found a significant 36% higher risk of SAEs, which included deaths and many life-threatening conditions in the vaccinated participants. Official SAEs for other vaccines average around only 1-2 per million. Fraiman et alestimated 1,250 SEAs per million vaccines, exceeding that benchmark by “at least 600-fold.” After the vaccine rollout, analyses of two large drug safety reporting systems in the U.S. and Europe identified signals for myocardial infarction, pulmonary embolism, cardio-respiratory arrest, cerebral infarction, and cerebral hemorrhage associated with both mRNA vaccines, along with ischemic stroke. And millions of AEs have been reported to those systems. Another study by Skidmore et al. estimated the total number of fatalities from the vaccines in 2021 alone was 289,789. Autopsy studies have also provided additional evidence of serious harms, including evidence that most COVID-19 mRNA vaccine-related deaths resulted from injury to the cardiovascular system. In multiple autopsy studies, German pathologist Aren Burkhardt documented the presence of vaccine-mRNA-produced spike proteins in blood vessel walls and brain tissues. This research helps to explain documented vaccine-induced toxicities affecting the nervous, immune, reproductive and other systems. The Pfizer data also showed an overwhelming number of adverse effects. According to a confidential document released in August 2022, Pfizer had documented approximately 1.6 million AEs affecting nearly every organ system, and one-third of them were classified as serious. In Pfizer’s trial, Michels and colleagues found a nearly 4-fold increase (OR 3.7, 95%CI 1.02-13.2, p = 0.03) in serious cardiac events (e.g., heart attack, acute coronary syndrome) in the vaccine group. Neither the original trial report nor Pfizer’s Summary Clinical Safety report acknowledged or commented on this safety signal. “The serious adverse events are all well documented,” Mead said. “Yet it’s surprising to see so many in the medical field continue to ignore or dismiss outright the latter half of the equation when considering all cause mortality trends.” 5. The failure to appropriately test for safety and toxicity poses serious problems. Researchers have raised concerns that the mRNA technology is inherently unstable and difficult to store, which leads to batch variability and contamination linked to different rates of AEs. Recent findings by McKernan et al. that found Pfizers’ mRNA vaccines are contaminated with plasmid DNA that shouldn’t be present — and wasn’t present in the vaccines used in the trials – raising serious safety issues. That’s because “Process 1,” used in the trials to generate the vaccines involved in vitro transcription of synthetic DNA — essentially a “clean” process. However, that process isn’t viable for mass production, so the manufacturers used “Process 2,” which involves using E. coli bacteria to replicate the plasmids. Removing plasmids E coli. can result in residual plasmids in the vaccines and the effects of their presence is unknown. McKernan’s work also revealed the presence of DNA from simian virus 40 (SV40), an oncogenic DNA virus originally isolated in 1960 from contaminated polio vaccines, induces lymphomas, brain tumors, and other malignancies in laboratory animals, raising other safety concerns. Researchers from Cambridge published a paper in Nature in December 2023, where they found an inherent defect in the modified RNA instructions for the spike protein in COVID-19 immunizations that causes the machinery that translates the gene to the spike protein to “slip” about 10% of the time This process creates “frameshifts” that cause cells to produce “off-target” proteins in addition to the spike. These proteins, which developers either failed to look for or did not report to regulators, cause undesirable immune responses whose long-term effects are unknown. 6. There are many different possible biological mechanisms that cause AEs and vaccine ineffectiveness. The review points readers to a series of papers that explain a number of different theories to explain the high number of AEs from the COVID-19 mRNA vaccines. “The mechanisms of molecular mimicry, antigen cross-reactivity, pathogenic priming, viral reactivation, immune exhaustion, and other factors related to immune dysfunction all reinforce the biological plausibility for vaccine-induced pathogenesis of malignant and autoimmune diseases,” they wrote. And these mechanisms of immune activation are distinct from the body’s response to a viral infection. They also note the toxic effects of the primary adjuvant, PEG, and of the spike protein itself. They close their analysis of the vaccines with a complex explanation for the different immunological basis for protection provided by the vaccines versus natural immunity through infection. They explain the mechanisms for vaccine failure and problems generated by the ability for the mRNA vaccines to perpetuate the emergence of new variants. https://childrenshealthdefense.org/defender/scientists-global-moratorium-mrna-vaccines-removal-childhood-schedule/ https://donshafi911.blogspot.com/2024/01/scientists-call-for-global-moratorium.html
    CHILDRENSHEALTHDEFENSE.ORG
    Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule
    A review paper published last week in the journal Cureus is the first peer-reviewed paper to call for a global moratorium on the COVID-19 mRNA vaccines. The authors say that reanalyzed data from the vaccine makers’ trials and high rates of serious post-injection injuries indicate the mRNA gene therapy vaccines should not have been authorized for use.
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  • 🚨 ‘Futile + Dangerous’: Cameroon First of 20 African Countries to Roll Out GSK’s Malaria Vaccine for Babies

    Cameroon this week launched a campaign to vaccinate 250,000 babies, beginning at age 6 months, with GlaxoSmithKline’s malaria vaccine — a shot that even the Bill & Melinda Gates Foundation said won’t work.

    https://childrenshealthdefense.org/defender/cameroon-africa-gsk-malaria-vaccine-babies/

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    🚨 ‘Futile + Dangerous’: Cameroon First of 20 African Countries to Roll Out GSK’s Malaria Vaccine for Babies Cameroon this week launched a campaign to vaccinate 250,000 babies, beginning at age 6 months, with GlaxoSmithKline’s malaria vaccine — a shot that even the Bill & Melinda Gates Foundation said won’t work. https://childrenshealthdefense.org/defender/cameroon-africa-gsk-malaria-vaccine-babies/ Join ➡️ @ShankaraChetty
    CHILDRENSHEALTHDEFENSE.ORG
    ‘Futile and Dangerous’: Cameroon First of 20 African Countries to Roll Out GSK’s Malaria Vaccine for Babies
    Cameroon this week launched a campaign to vaccinate 250,000 babies, beginning at age 6 months, with GlaxoSmithKline’s malaria vaccine — a shot that even the Bill & Melinda Gates Foundation said won’t work.
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  • MMR Vaccine Debate Heats Up as Media Claim ‘Vaccine Hesitancy’ to Blame for Recent Outbreaks
    As major news outlets linked reports of measles cases in the U.S. and U.K. to declining vaccine rates, experts told The Defender that case numbers in the U.S. have been extremely low for decades and the very minor variations in vaccination rates do not make a difference.

    Brenda Baletti, Ph.D.
    mmr vaccine media outbreaks feature
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    Measles outbreaks are in the news again.

    In the U.S., local health departments and media reported about 16 cases of measles between December 2023 and January. The outbreaks occurred in Philadelphia, New Jersey, Georgia and Washington.

    In the United Kingdom, the UK Health Security Agency reported 209 cases between January and November 2023 and about 319 cases between October 2023 and the present.

    Media blamed international travel and declining vaccination rates among children as “probably” behind the outbreaks.

    But Dr. Liz Mumper, a pediatrician, told The Defender it doesn’t make sense to assume the unvaccinated are to blame. She said cyclical outbreaks still occur even in populations with nearly 100% vaccination, such as college students.

    Dr. Paul Thomas, a retired pediatrician and author of “The Vaccine-Friendly Plan: Dr. Paul’s Safe and Effective Approach to Immunity and Health-from Pregnancy Through Your Child’s Teen Years Paperback,” told The Defender some cases of measles are reported every year. Despite the hype around the recent outbreaks, he said, “There have not been any significant measles outbreaks in the U.S. for decades.”

    The largest recent national spike in measles cases occurred in 2019 when 1,274 cases were reported, according to the Centers for Disease Control and Prevention (CDC). It was the worst year for measles in the U.S. since 1992.

    Since 2019, the number of cases reported has been significantly lower: In 2020, there were 13 cases, in 2021, 49 cases, in 2022 there were 121 cases and in 2023, there were 56 cases. The post-2019 numbers also tend to be lower than the numbers from 2000-2018, which averaged around 200 per year.


    Credit: Centers for Disease Control and Prevention
    Measles is a contagious childhood viral disease characterized by a cough, runny nose and fever, followed by a generalized rash.

    It was declared to be eliminated in the U.S. in 2000 — meaning there was no continuous transmission.

    Mortality from measles in the U.S. declined significantly during the 20th century — 98% from 1900 to 1963, before the measles vaccine was introduced — due to advances in living conditions, healthcare and nutrition, according to Physicians for Informed Consent.

    Since 2000, there have been only four measles deaths in the Americas — three in 2000 and one in 2022, according to a November 2023 CDC report.

    The overwhelming majority of the approximately 130,000 measles deaths annually occur in countries in the global south that have weak health infrastructures, according to the World Health Organization (WHO). Those deaths, along with measles hospitalizations in the global north, are associated with vitamin A deficiency.

    “Measles can be deadly if a child does not have access to safe water and medical care,” Mumper said. “In developed countries, fatalities from measles are very rare.”

    Effective treatments include vitamin A in high doses and attention to hydration status, Mumper said.

    “Many natural methods to help the body fight viruses, like extra vitamin D and vitamin C are effective but not widely recommended by mainstream medicine,” she added.

    Prior to the introduction of the vaccine in the U.S. in 1963, most people contracted measles and gained lifetime immunity, and the number of deaths had dropped to 0.9 per 100,000 for children under age 10.

    The vaccines significantly reduced the number of reported measles cases, with efficacy rates that can be upwards of 95%, Thomas said. However, he added immunity from the vaccines wanes over time.

    “From a mechanistic standpoint, the lifelong 100% natural immunity comes when measles is caught through respiratory spread. Giving a vaccine by injection may be an inherently poor substitute for Mother Nature,” Mumper said.

    Approximately 83% of children globally received one dose of the measles, mumps and rubella (MMR) vaccine by their first birthday in 2022.

    RFK Jr. and Brian Hooker Vax-Unvax
    RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax”

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    Hotez, Offit blame the ‘anti-vaxers’ for measles outbreaks

    Although case numbers have declined in the U.S. since 2020, and the recently reported cases were either among adults or children who may be too young to have completed the MMR vaccine schedule, news reports about the outbreaks consistently link them to lower post-pandemic vaccination rates among kindergarteners.

    The CDC recommends two doses of the MMR vaccine, with the first dose at 12 to 15 months old and the second dose between ages 4 and 6.

    The agency reported that from the 2019-20 school year to the 2021-22 school year vaccination rates for state-required vaccines among kindergarten children declined from approximately 95% to approximately 93%, and the exemption rate increased to 3.0%.

    CDC data going back to 2011 show that rates typically vary from year-to-year, but consistently stay above 93%.

    Thomas said the drop has been minimal and “given the loss of immunity in both children and adults in the vaccinated, this minor reduction in MMR uptake by children is not going to make a difference [in infection rates].”

    Dr. Peter Hotez, a go-to “expert” for mainstream media on vaccines — and a vaccine developer and patent holder himself, who has repeatedly smeared vaccine safety advocates as “anti-science aggressors” — told ABC and CBS News that he thought the sporadic outbreaks were likely a result of lowered vaccination rates and that they were going to get worse.

    “We’re just seeing now, this is the tip of the iceberg,” Hotez said. “We’re going to be seeing this in communities across the United States in the coming weeks and months because of the spillover of the U.S. anti-vaccine movement of childhood immunizations.”

    According to ABC — quoting Hotez, Dr. Paul Offit and the Mayo Clinic’s Dr. Gregory Poland — this is due to vaccine “misinformation” linking vaccines and autism, combined with the politicization of the COVID-19 vaccines, which Hotez said caused “an acceleration of anti-vaccine sentiments.”

    Hotez has been making these arguments for years, writing a New York Times op-ed in 2020 claiming there is no link between vaccines and autism and blaming unvaccinated people for infectious disease outbreaks.

    Offit said given the vaccine’s efficacy, it was “unconscionable” for parents to forgo vaccination for their children.

    But there is a significant and growing body of evidence suggesting the MMR vaccine can cause autism in certain susceptible children. That includes evidence that U.S. Department of Justice lawyers suppressed testimony by their own expert witness making the link, and evidence from whistleblower William Thompson, Ph.D., that the CDC covered up its own data showing a link between vaccines and autism.

    In a Substack post from 2022, Dr. Peter McCullough evaluated a study on the “Association Between Vaccine Refusal and Vaccine-Preventable Diseases in the United States,” namely measles and pertussis.

    The study indicated that since measles was declared eradicated in 2000, there have been 18 published studies of 1,416 measles cases — 43.2% of the cases occurred in vaccinated people and no hospitalizations or deaths were reported.

    McCullough concluded:

    “Large fractions of ‘preventable disease outbreaks’ involving measles and pertussis occur because vaccines fail to provide adequate protection. Given the neuropsychiatric concerns over the MMR vaccine and the stochastic risk of allergic/immunologic reactions to any injection including components of (DTaP, Tdap) or MMR, the parental movement for vaccine choice is well justified.

    “For measles and pertussis, the vaccines convey imperfect protection and breakthrough infection (vaccine failure) should receive considerable ‘blame’ by public health researchers.”

    Mumper said the vaccine schedule has changed, lowering efficacy. “Vaccine efficacy was calculated to be ~94% when the first dose was given at 15 months,” she said.

    “Now babies are scheduled to get the first dose at 12 months (only 85% efficacy) and their second dose at kindergarten.”

    Mumper added, “People with different genotypes respond differently to MMR vaccines, so there is variable measles transmission depending on the individual’s immune response. Up to 10% of the population does not develop enough protective antibodies.”

    New outbreaks lead push for adults to get another MMR

    Derek Gatherer, Ph.D., a lecturer in biomedical and life sciences at Lancaster University who is funded by the U.K. government to study “vaccine hesitancy,” said the solution to the problem of measles outbreaks is more vaccination — for adults.

    Gatherer published a recent article in The Conversation blaming the vaccine-hesitant for the outbreaks. He argued that even adults who are already vaccinated should consider getting more MMR jabs.

    “Measles is the most infectious disease known to science — adults should consider getting another MMR vaccine,” he declared.

    Gatherer conceded that the measles risk to adults is extremely small, but said “adult MMR is still worthwhile as it goes beyond just protecting the person who receives the vaccination,” stopping asymptomatic infections from spreading.

    Thomas said it is not common to recommend booster shots to adults for illnesses they were vaccinated for as children. “However,” he added, “the pharmaceutical industry, backed by the CDC, has been looking at the adult population as an untapped resource to expand market share and penetration.”

    Reports of cases rising in the UK

    In the U.K., measles was considered eliminated in 2016, but it resurfaced in 2018.

    U.K. MMR vaccination rates average 85%, down from a peak of 88.6% in 2014, with some locations reporting rates as low as 74%.

    According to The Guardian, “Most experts agree that misinformation about the MMR jab is very unlikely to play a significant role in declining vaccination rates.

    “It is too easy to blame anti-vaccine sentiment for the measles outbreaks,” Helen Bedford, professor of children’s health at the University College London Great Ormond Street Institute of Child Health told the paper. “Although some mistrust of vaccines may play a small part, research shows that parental vaccine confidence remains high.”

    Experts there pointed to pandemic disruptions in vaccination, concerns among Muslim and Jewish communities about the use of porcine gelatin in the vaccine, and also the fact that because the disease is so rare, people are less concerned about possible risks.

    England’s National Health Service is launching an MMR vaccination campaign, the BBC reported, contacting 4 million parents via text, email or letter to inform them their child has not had one or two doses of the vaccine.




    🚨 MMR Vaccine Debate Heats Up as Media Claim ‘Vaccine Hesitancy’ to Blame for Recent Outbreaks
    “Many natural methods to help the body fight viruses, like extra vitamin D + vitamin C are effective but not widely recommended by mainstream medicine." — Dr. Liz Mumper
    https://childrenshealthdefense.org/defender/mmr-vaccine-media-measles-outbreaks
    MMR Vaccine Debate Heats Up as Media Claim ‘Vaccine Hesitancy’ to Blame for Recent Outbreaks As major news outlets linked reports of measles cases in the U.S. and U.K. to declining vaccine rates, experts told The Defender that case numbers in the U.S. have been extremely low for decades and the very minor variations in vaccination rates do not make a difference. Brenda Baletti, Ph.D. mmr vaccine media outbreaks feature Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. Measles outbreaks are in the news again. In the U.S., local health departments and media reported about 16 cases of measles between December 2023 and January. The outbreaks occurred in Philadelphia, New Jersey, Georgia and Washington. In the United Kingdom, the UK Health Security Agency reported 209 cases between January and November 2023 and about 319 cases between October 2023 and the present. Media blamed international travel and declining vaccination rates among children as “probably” behind the outbreaks. But Dr. Liz Mumper, a pediatrician, told The Defender it doesn’t make sense to assume the unvaccinated are to blame. She said cyclical outbreaks still occur even in populations with nearly 100% vaccination, such as college students. Dr. Paul Thomas, a retired pediatrician and author of “The Vaccine-Friendly Plan: Dr. Paul’s Safe and Effective Approach to Immunity and Health-from Pregnancy Through Your Child’s Teen Years Paperback,” told The Defender some cases of measles are reported every year. Despite the hype around the recent outbreaks, he said, “There have not been any significant measles outbreaks in the U.S. for decades.” The largest recent national spike in measles cases occurred in 2019 when 1,274 cases were reported, according to the Centers for Disease Control and Prevention (CDC). It was the worst year for measles in the U.S. since 1992. Since 2019, the number of cases reported has been significantly lower: In 2020, there were 13 cases, in 2021, 49 cases, in 2022 there were 121 cases and in 2023, there were 56 cases. The post-2019 numbers also tend to be lower than the numbers from 2000-2018, which averaged around 200 per year. Credit: Centers for Disease Control and Prevention Measles is a contagious childhood viral disease characterized by a cough, runny nose and fever, followed by a generalized rash. It was declared to be eliminated in the U.S. in 2000 — meaning there was no continuous transmission. Mortality from measles in the U.S. declined significantly during the 20th century — 98% from 1900 to 1963, before the measles vaccine was introduced — due to advances in living conditions, healthcare and nutrition, according to Physicians for Informed Consent. Since 2000, there have been only four measles deaths in the Americas — three in 2000 and one in 2022, according to a November 2023 CDC report. The overwhelming majority of the approximately 130,000 measles deaths annually occur in countries in the global south that have weak health infrastructures, according to the World Health Organization (WHO). Those deaths, along with measles hospitalizations in the global north, are associated with vitamin A deficiency. “Measles can be deadly if a child does not have access to safe water and medical care,” Mumper said. “In developed countries, fatalities from measles are very rare.” Effective treatments include vitamin A in high doses and attention to hydration status, Mumper said. “Many natural methods to help the body fight viruses, like extra vitamin D and vitamin C are effective but not widely recommended by mainstream medicine,” she added. Prior to the introduction of the vaccine in the U.S. in 1963, most people contracted measles and gained lifetime immunity, and the number of deaths had dropped to 0.9 per 100,000 for children under age 10. The vaccines significantly reduced the number of reported measles cases, with efficacy rates that can be upwards of 95%, Thomas said. However, he added immunity from the vaccines wanes over time. “From a mechanistic standpoint, the lifelong 100% natural immunity comes when measles is caught through respiratory spread. Giving a vaccine by injection may be an inherently poor substitute for Mother Nature,” Mumper said. Approximately 83% of children globally received one dose of the measles, mumps and rubella (MMR) vaccine by their first birthday in 2022. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now Hotez, Offit blame the ‘anti-vaxers’ for measles outbreaks Although case numbers have declined in the U.S. since 2020, and the recently reported cases were either among adults or children who may be too young to have completed the MMR vaccine schedule, news reports about the outbreaks consistently link them to lower post-pandemic vaccination rates among kindergarteners. The CDC recommends two doses of the MMR vaccine, with the first dose at 12 to 15 months old and the second dose between ages 4 and 6. The agency reported that from the 2019-20 school year to the 2021-22 school year vaccination rates for state-required vaccines among kindergarten children declined from approximately 95% to approximately 93%, and the exemption rate increased to 3.0%. CDC data going back to 2011 show that rates typically vary from year-to-year, but consistently stay above 93%. Thomas said the drop has been minimal and “given the loss of immunity in both children and adults in the vaccinated, this minor reduction in MMR uptake by children is not going to make a difference [in infection rates].” Dr. Peter Hotez, a go-to “expert” for mainstream media on vaccines — and a vaccine developer and patent holder himself, who has repeatedly smeared vaccine safety advocates as “anti-science aggressors” — told ABC and CBS News that he thought the sporadic outbreaks were likely a result of lowered vaccination rates and that they were going to get worse. “We’re just seeing now, this is the tip of the iceberg,” Hotez said. “We’re going to be seeing this in communities across the United States in the coming weeks and months because of the spillover of the U.S. anti-vaccine movement of childhood immunizations.” According to ABC — quoting Hotez, Dr. Paul Offit and the Mayo Clinic’s Dr. Gregory Poland — this is due to vaccine “misinformation” linking vaccines and autism, combined with the politicization of the COVID-19 vaccines, which Hotez said caused “an acceleration of anti-vaccine sentiments.” Hotez has been making these arguments for years, writing a New York Times op-ed in 2020 claiming there is no link between vaccines and autism and blaming unvaccinated people for infectious disease outbreaks. Offit said given the vaccine’s efficacy, it was “unconscionable” for parents to forgo vaccination for their children. But there is a significant and growing body of evidence suggesting the MMR vaccine can cause autism in certain susceptible children. That includes evidence that U.S. Department of Justice lawyers suppressed testimony by their own expert witness making the link, and evidence from whistleblower William Thompson, Ph.D., that the CDC covered up its own data showing a link between vaccines and autism. In a Substack post from 2022, Dr. Peter McCullough evaluated a study on the “Association Between Vaccine Refusal and Vaccine-Preventable Diseases in the United States,” namely measles and pertussis. The study indicated that since measles was declared eradicated in 2000, there have been 18 published studies of 1,416 measles cases — 43.2% of the cases occurred in vaccinated people and no hospitalizations or deaths were reported. McCullough concluded: “Large fractions of ‘preventable disease outbreaks’ involving measles and pertussis occur because vaccines fail to provide adequate protection. Given the neuropsychiatric concerns over the MMR vaccine and the stochastic risk of allergic/immunologic reactions to any injection including components of (DTaP, Tdap) or MMR, the parental movement for vaccine choice is well justified. “For measles and pertussis, the vaccines convey imperfect protection and breakthrough infection (vaccine failure) should receive considerable ‘blame’ by public health researchers.” Mumper said the vaccine schedule has changed, lowering efficacy. “Vaccine efficacy was calculated to be ~94% when the first dose was given at 15 months,” she said. “Now babies are scheduled to get the first dose at 12 months (only 85% efficacy) and their second dose at kindergarten.” Mumper added, “People with different genotypes respond differently to MMR vaccines, so there is variable measles transmission depending on the individual’s immune response. Up to 10% of the population does not develop enough protective antibodies.” New outbreaks lead push for adults to get another MMR Derek Gatherer, Ph.D., a lecturer in biomedical and life sciences at Lancaster University who is funded by the U.K. government to study “vaccine hesitancy,” said the solution to the problem of measles outbreaks is more vaccination — for adults. Gatherer published a recent article in The Conversation blaming the vaccine-hesitant for the outbreaks. He argued that even adults who are already vaccinated should consider getting more MMR jabs. “Measles is the most infectious disease known to science — adults should consider getting another MMR vaccine,” he declared. Gatherer conceded that the measles risk to adults is extremely small, but said “adult MMR is still worthwhile as it goes beyond just protecting the person who receives the vaccination,” stopping asymptomatic infections from spreading. Thomas said it is not common to recommend booster shots to adults for illnesses they were vaccinated for as children. “However,” he added, “the pharmaceutical industry, backed by the CDC, has been looking at the adult population as an untapped resource to expand market share and penetration.” Reports of cases rising in the UK In the U.K., measles was considered eliminated in 2016, but it resurfaced in 2018. U.K. MMR vaccination rates average 85%, down from a peak of 88.6% in 2014, with some locations reporting rates as low as 74%. According to The Guardian, “Most experts agree that misinformation about the MMR jab is very unlikely to play a significant role in declining vaccination rates. “It is too easy to blame anti-vaccine sentiment for the measles outbreaks,” Helen Bedford, professor of children’s health at the University College London Great Ormond Street Institute of Child Health told the paper. “Although some mistrust of vaccines may play a small part, research shows that parental vaccine confidence remains high.” Experts there pointed to pandemic disruptions in vaccination, concerns among Muslim and Jewish communities about the use of porcine gelatin in the vaccine, and also the fact that because the disease is so rare, people are less concerned about possible risks. England’s National Health Service is launching an MMR vaccination campaign, the BBC reported, contacting 4 million parents via text, email or letter to inform them their child has not had one or two doses of the vaccine. 🚨 MMR Vaccine Debate Heats Up as Media Claim ‘Vaccine Hesitancy’ to Blame for Recent Outbreaks “Many natural methods to help the body fight viruses, like extra vitamin D + vitamin C are effective but not widely recommended by mainstream medicine." — Dr. Liz Mumper https://childrenshealthdefense.org/defender/mmr-vaccine-media-measles-outbreaks
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    MMR Vaccine Debate Heats Up as Media Claim ‘Vaccine Hesitancy’ to Blame for Recent Outbreaks
    As major news outlets linked reports of measles cases in the U.S. and U.K. to declining vaccine rates, experts told The Defender that case numbers in the U.S. have been extremely low for decades and the very minor variations in vaccination rates do not make a difference.
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