The Older True Great Awakening with 105 pages

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It was the Queen and now the Pope ... COINCIDENCE??

All LIES will be revealed.

When you find out the TRUTH on the POPE, you will ne more than SHOCKED. I guarantee that!

article: https://www.newsmax.com/platinum/vatican-pope-francis-health-conclave/2021/12/07/id/1047663/

 

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Add one more to the list. 

 

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The scientific community speaks out against the health policy of the authorities: the declaration of Great Barrington (USA) against massive injections of mRNA has collected 870.000 signatures.

While the President of the French Republic meets this Monday, December 6, a new Council of Defense to fight against the spread of the epidemic of Covid-19, more and more voices are raised against the health policy completely crazy of the authorities which aims to vaccinate more and more the population. After the third dose of vaccine imposed, under penalty of deactivation of the health pass! There is now the question of vaccinating children from 5 to 11 years old. A decision that would be very serious according to many doctors and researchers that we have reported here.

Serious side effects

Mass vaccination with a still experimental messenger RNA vaccine has long worried the scientific community. As of October 4, 2020, three high-level scientists, Prof. Martin Kulldorff, professor of medicine at Harvard University, biostatistician and epidemiologist, specializing in the detection and monitoring of infectious disease outbreaks and in the evaluation of vaccine safety. Dr. Sunetra Gupta, professor at Oxford University, an epidemiologist specializing in immunology, vaccine development and mathematical modeling of infectious diseases. And Dr. Jay Bhattacharya, a professor at Stanford University School of Medicine, a physician, epidemiologist, health economist, and public health policy expert specializing in infectious diseases and vulnerable populations, recommended an alternative approach to Covid-19 in what was called the Great Barrington Declaration. Because they are very concerned about the side effects of mass vaccination on populations.
What do they advocate? A “focused” protection. That is to say, to protect as much as possible the elderly, the infirm, the frail and to leave the others to live normally until the society reaches the collective immunity. However, mass vaccination by mRNA makes this collective immunity impossible.
One of the original co-signatories was Dr. Simon Thornley, an epidemiologist and biostatistician at the University of Auckland. The Great Barrington Declaration has since been signed by 60,000 physicians and scientists and is becoming increasingly well known around the world. A petition has so far gathered 870,000 signatures of support.

The Great Barrington Declaration

“The Great Barrington Declaration – As infectious disease epidemiologists and public health scientists we have grave concerns about the damaging physical and mental health impacts of the prevailing COVID-19 policies, and recommend an approach we call Focused Protection.

Coming from both the left and right, and around the world, we have devoted our careers to protecting people. Current lockdown policies are producing devastating effects on short and long-term public health. The results (to name a few) include lower childhood vaccination rates, worsening cardiovascular disease outcomes, fewer cancer screenings and deteriorating mental health – leading to greater excess mortality in years to come, with the working class and younger members of society carrying the heaviest burden. Keeping students out of school is a grave injustice.

Keeping these measures in place until a vaccine is available will cause irreparable damage, with the underprivileged disproportionately harmed.

Fortunately, our understanding of the virus is growing. We know that vulnerability to death from COVID-19 is more than a thousand-fold higher in the old and infirm than the young. Indeed, for children, COVID-19 is less dangerous than many other harms, including influenza.

As immunity builds in the population, the risk of infection to all – including the vulnerable – falls. We know that all populations will eventually reach herd immunity – i.e. the point at which the rate of new infections is stable – and that this can be assisted by (but is not dependent upon) a vaccine. Our goal should therefore be to minimize mortality and social harm until we reach herd immunity.

The most compassionate approach that balances the risks and benefits of reaching herd immunity, is to allow those who are at minimal risk of death to live their lives normally to build up immunity to the virus through natural infection, while better protecting those who are at highest risk. We call this Focused Protection.

Adopting measures to protect the vulnerable should be the central aim of public health responses to COVID-19. By way of example, nursing homes should use staff with acquired immunity and perform frequent testing of other staff and all visitors. Staff rotation should be minimized. Retired people living at home should have groceries and other essentials delivered to their home. When possible, they should meet family members outside rather than inside. A comprehensive and detailed list of measures, including approaches to multi-generational households, can be implemented, and is well within the scope and capability of public health professionals.

Those who are not vulnerable should immediately be allowed to resume life as normal. Simple hygiene measures, such as hand washing and staying home when sick should be practiced by everyone to reduce the herd immunity threshold. Schools and universities should be open for in-person teaching. Extracurricular activities, such as sports, should be resumed. Young low-risk adults should work normally, rather than from home. Restaurants and other businesses should open. Arts, music, sport and other cultural activities should resume. People who are more at risk may participate if they wish, while society as a whole enjoys the protection conferred upon the vulnerable by those who have built up herd immunity.”

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https://thepulse.one/2021/12/07/3d-printed-assisted-suicide-pod-is-now-legal-in-switzerland/

 

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The TRUTH is also very FUNNY!!

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You were right Mr. President, the MSM are the ENEMY OF THE PEOPLE!!

 

 

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https://generaldispatch.whatfinger.com/wisconsin-hearing-going-on-15700-voters-in-wisconsin-have-the-same-voter-registration-number-more/

 

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Jab Causing More Deaths Due To Decreased Immune System – Funeral Director John O’Looney
BY RED VOICE MEDIA
DECEMBER 8, 2021

https://www.redvoicemedia.com/video/2021/12/jab-causing-more-deaths-due-to-decreased-immune-system-funeral-director-john-olooney/

 

 

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"The Lil' Talk Show" w/Brad Published December 9, 2021

TIP: You might want to try to listen to the longer videos by changing the speeds to 1.25 or 1.5 or even 1.75 to save time. > Click on setting "Star" and then select SPEED and then you can select the speed you want. 

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I hope you realize that the MSM pushed his so called innocence for over 2 years.

Thank God the TRUTH finally came out.
I can't wait until the MSM are ALL charged and held accountable for the millions of crimes THEY have committed over the years. 

https://www.msn.com/en-us/news/crime/jussie-smollett-found-guilty-in-alleged-hate-crime-hoax-trial/ar-AARF0tn

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3 hours ago, Pompeii said:

I hope you realize that the MSM pushed his so called innocence for over 2 years.

Thank God the TRUTH finally came out.
I can't wait until the MSM are ALL charged and held accountable for the millions of crimes THEY have committed over the years. 

https://www.msn.com/en-us/news/crime/jussie-smollett-found-guilty-in-alleged-hate-crime-hoax-trial/ar-AARF0tn

 

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This will tell you why most of these politicians (95%) & MSM (99%) are THE BIGGEST LIARS ON THE FACE OF THIS EARTH!! They must pay for these CRIMES against us, WE THE PEOPLE!! 

Those aged well.... Smollett was found guilty of a hoax hate crime on all counts apart from one. Count 6 reportedly refers to Smollett reporting on Feb. 14, 2019, to detective Robert Graves that he’d been a victim of an aggravated battery.

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The Ivermectin Story >> (Short Film) 

 First discovered in 1973, ivermectin won the Nobel Prize in 2015. What makes this drug so extraordinary? Please watch the video below because it is the TRUTH you are not hearing anywhere.

Ivermectin is one of the safest drugs out there. Most of the MSM, Hospitals & Doctors are lying to you about this drug. >>> Ivermectin CURES COVID!

ALL LIES WILL BE REVEALED

 

 

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Pennsylvania Supreme Court throws out Wolf administration’s school mask mandate

https://www.mcall.com/news/breaking/mc-pa-virus-outbreak-pennsylvania-mask-mandate-20211210-eoy7dblqpfe6hfy7e6qvvatgby-story.html

https://www.msn.com/en-us/news/us/pa-supreme-court-says-school-mask-mandate-is-overturned/ar-AARHzzY

 

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Dr. Byram Bridle: Viral Immunologist Debunks Mask Protect People From Covid

 

This might work?? 

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Exposed: Confidential Documents Show Pfizer’s Jab Blackmail Of Governments Around The World

https://www.redvoicemedia.com/2021/12/exposed-confidential-documents-show-pfizers-jab-blackmail-of-governments-around-the-world-video/

 

 

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https://madisonarealymesupportgroup.com/2021/10/21/groundbreaking-nebraska-ag-says-doctors-can-legally-prescribe-ivermectin-hcq-for-covid-calls-out-fda-cdc-fauci-media-for-fueling-confusion-misinformation/

Spoiler

GROUNDBREAKING: NEBRASKA AG SAYS DOCTORS CAN LEGALLY PRESCRIBE IVERMECTIN, HCQ FOR COVID, CALLS OUT FDA, CDC, FAUCI, MEDIA FOR ‘FUELING CONFUSION AND MISINFORMATION’

At the request of the Nebraska Department of Health, on Oct. 15, Nebraska Attorney General Doug Peterson issued a legal opinion that Nebraska healthcare providers can legally prescribe ivermectin and hydroxychloroquine for the treatment of COVID, so long as they obtain informed consent from the patient.

By Megan Redshaw 

Few subjects have been more controversial than ivermectin and hydroxychloroquine — two long-established, inexpensive medications widely and successfully used in many parts of the world for the prevention and treatment of COVID.

By contrast, the use of both medications against COVID has been largely suppressed in the U.S, where doctors have been threatened and punished for prescribing them.

On Oct. 15, Nebraska Attorney General (AG) Doug Peterson issued a legal opinion that Nebraska healthcare providers can legally prescribe off-label medications like ivermectin and hydroxychloroquine for the treatment of COVID, so long as they obtain informed consent from the patient.

However, if they did neglect to obtain consent, deceive, prescribe excessively high doses or other misconduct, they could be subject to discipline, Peterson wrote.

The AG’s office emphasized it was not recommending any specific treatment for COVID. “That is not our role,” Peterson wrote. “Rather, we address only the off-label early treatment options discussed in this opinion and conclude that the available evidence suggests they might work for some people.”

Peterson said allowing physicians to consider early treatments will free them to evaluate additional tools that could save lives, keep patients out of the hospital and provide relief for our already strained healthcare system.

The opinion, based on an assessment of relevant scientific literature, was rendered in response to a request by Dannette Smith, CEO of the Nebraska Department of Health and Human Services.

Smith asked the AG’s office to look into whether doctors could face discipline or legal action under Nebraska’s Uniform Credential Act (UCA) — meant to protect public health, safety and welfare — if they prescribed ivermectin or hydroxychloroquine.

“After receiving your question and conducting our investigation, we have found significant controversy and suspect information about potential COVID-19 treatments,” Peterson wrote.

For example, a paper published in the Lancet — one of the most prestigious medical journals in the world — denounced hydroxychloroquine as dangerous, yet the statistics were flawed and the authors refused to provide analyzed data.

The paper was retracted, but not before countries stopped using the drug and trials were cancelled or interrupted.

“The Lancet’s own editor-in-chief admitted that the paper was a ‘fabrication,’ a ‘monumental fraud’ and a ‘shocking example of research misconduct’ in the middle of a global health emergency,” Peterson wrote in the opinion.

A recently published paper on COVID recognized that “for reasons that are yet to be clarified,” early treatment has not been emphasized despite numerous U.S. healthcare providers advocating for early treatment and “scores of treating and academic physicians” — who have published papers in well respected journals — urging early interventions.

Peterson cited numerous studies showing ivermectin and hydroxychloroquine reduced mortality by up to 75% or more when used as a preventative or prophylaxis for COVID, suggesting hundreds of thousands of lives could have been saved had the drugs been widely used in America.

“Every citizen — Democrat or Republican — should be grateful for Doug Peterson’s thoughtful and courageous counteroffensive against the efforts of Big Pharma, its captive federal regulators, and its media and social media allies to silence doctors and deny Americans life-saving treatments,” Robert F. Kennedy Jr., chairman of Children’s Health Defense, told The Defender via email.

“We finally have a leader who puts constitutional rights, peer-reviewed science and human health above industry profits. Doug Peterson is uncowed and unbowed — a genuine hero on horseback for all Americans.” Kennedy said.

Children’s Health Defense President Mary Holland agreed. “This Nebraska AG opinion lets doctors get back to being doctors — without being second-guessed by government, pharmacists and others interfering in the crucial doctor-patient relationship,” Holland said.

Although the AG’s office did not rule out the possibility that other off-label drugs might show promise — either now or in the future — as a prophylaxis or treatment against COVID, it confined its opinion to ivermectin and hydroxychloroquine for the sake of brevity.

Nebraska AG highlights science on ivermectin

In his legal opinion, Peterson concluded evidence showed ivermectin demonstrated striking effectiveness in preventing and treating COVID, and any side effects were primarily minor and transient. “Thus, the UCA does not preclude physicians from considering ivermectin for the prevention or treatment of COVID,” Peterson wrote.

In the decade leading up to the COVID pandemic, Peterson found numerous studies showing ivermectin’s antiviral acti­vity against several RNA viruses by blocking the nuclear trafficking of viral proteins, adding to 50 years of research confirming ivermectin’s antiviral effects.

In addition, safety data for ivermectin showed side effects were “vanishingly small.” The latest statistics available through VigiAccess reported only 5,674 adverse drug reac­tions to ivermectin between 1992 and October 13, 2021, an “incredibly low” number given that 3.7 billion doses have been administered since the 1980s, Peterson wrote.

Peterson cited several studies showing ivermectin led to improvement of COVID outcomes when used in early treatment or as a prophylaxis, while noting many studies with negative findings about ivermectin “excluded most available evidence,” cherry picked data within studies, misreported data, made unsupported assertions of adverse reactions to ivermectin and had “conclusions that did follow from evidence.”

Peterson also found that epidemiological evidence for ivermectin’s effectiveness, derived by analyzing COVID-related data from various states, countries or regions is instructive in the context of a global pandemic.

In one instance, a group of scholars analyzed data comparing COVID rates of countries that routinely administer ivermectin as a prophylaxis and countries that did not. The research showed “countries with routine mass drug administration of pro­phylactic … ivermectin have a significantly lower incidence of COVID-19.”

“This ‘highly significant’ correlation manifests itself not only ‘in a worldwide context’ but also when comparing African countries that regularly administer prophylactic ‘ivermectin against parasitic infections’ and African countries that do not,” Peterson wrote. “Based on these results, the researchers surmised that these results may be connected to ivermectin’s ability to inhibit SARS-CoV-2 replication, which likely leads to lower infection rates.”

Nebraska AG calls out FDA, Fauci on hypocrisy on ivermectin

Many U.S. health agencies have now addressed the use of ivermectin for COVID. The National Institutes of Health (NIH) has adopted a neutral position, choosing not to recommend for or against the use of ivermectin — a change from its position in January 2021 where it discouraged use of the drug for treatment of COVID.

Peterson wrote:

“The reason for the change is the NIH recognized several randomized trials and retrospective cohort studies of ivermectin use in patients with COVID-19 have been published in peer-reviewed journals. And some of those studies reported positive outcomes, including shorter time to resolution of disease manifestations that were attributed to COVID-19, greater reduction in inflammatory marker levels, shorter time to viral clearance, [and] lower mortality rates in patients who received ivermectin than in patients who received comparator drugs or placebo.”

Yet, on Aug. 29, Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases within the NIH, went on CNN and announced “there is no clinical evidence” that ivermectin works for the prevention or treatment of COVID. Fauci went on to reiterate that “there is no evidence whatsoever” that it works.

“This definitive claim directly contradicts the NIH’s recognition that ‘several randomized trials … published in peer-reviewed journals’ have reported data indicating that ivermectin is effective as a COVI D-19 treatment,” Peterson wrote.

In March 2021, the FDA posted a webpage, “Why You Should Not Use lvermectin to Treat or Prevent COVID-19.”

“Although the FDA’s concern was stories of some people using the animal form of ivermectin or excessive doses of the human form, the title broadly condemned any use of ivermectin in connection with COVID-19,” Peterson wrote. “Yet, there was no basis for its sweeping condemnation.”

Peterson wrote:

“Indeed, the FDA itself acknowledged on that very webpage (and continued to do so until the page changed on September 3, 2021) that the agency had not even ‘reviewed data to support use of ivermectin in COVID-19 patients to treat or to prevent COVID-19.’ But without reviewing the available data, which had long since been available and accumulating, it is unclear what basis the FDA had for denouncing ivermectin as a treatment or prophylaxis for COVID-19.

“On that same webpage, the FDA also declared that ‘[i]vermectin is not an anti-viral (a drug for treating viruses).’ It did so while another one of its webpages simultaneously cited a study in Antiviral Research that identified ivermectin as a medicine ‘previously shown to have broad-spectrum anti-viral activity.’”

“It is telling that the FDA deleted the line about ivermectin not being ‘anti-viral’ when it amended the first webpage on September 3, 2021,” Peterson noted.

Peterson said the FDA’s most controversial statement on ivermectin was made on Aug. 21, when it posted a link on Twitter to its “Why You Should Not Use lvermectin” webpage with this statement: “You are not a horse. You are not a cow. Seriously, y’all. Stop it.”

“This message is troubling not only because it makes light of a serious matter but also because it inaccurately implies that ivermectin is only for horses or cows,” Peterson wrote.

Peterson said the FDA has assailed ivermectin’s safety while ignoring the fact that physicians routinely prescribe medications for off-label use and that ivermectin is a “particularly well-tolerated medicine with an established safety record.”

Peterson added the FDA is ignoring several randomized controlled trials and at least one meta­analysis suggesting ivermectin is effective against COVID. He pointed out the Centers of Disease Control and Prevention has adopted a similar stance — unsupported by scientific evidence — and the media has fueled confusion and misinformation on the drug.

Peterson questions professional associations’ stance on ivermectin

Professional associations in the U.S. and internationally have adopted conflicting positions on ivermectin and COVID. The American Medical Association (AMA), American Pharmacists Association (APhA) and American Society of Health-System Pharmacists (ASHP) issued a statement in September strongly opposing the ordering, prescribing or dispensing of ivermectin to prevent or treat COVID outside of a clinical trial.

But their statement relied solely on the FDA’s and CDC’s suspect positions.

The AMA, APhA and ASHP also mentioned a statement by Merck — the original patent-holder — opposing the use of ivermectin for COVID because of a “concerning lack of safety data in the majority of studies.”

“But Merck, of all sources, knows that ivermectin is exceedingly safe, so the absence of safety data in recent studies should not be concerning to the company,” Peterson wrote.

Peterson called into question the objectivity of Merck in providing an opinion on ivermectin that U.S. health agencies are relying upon. “Why would ivermectin’s original patent holder go out of its way to question this medicine by creating the impression that it might not be safe?” Peterson asked. “There are at least two plausible reasons.”

Peterson explained:

“First, ivermectin is no longer under patent, so Merck does not profit from it anymore. That likely explains why Merck declined to ‘conduct clinical trials’ on ivermectin and COVID-19 when given the chance.

“Second, Merck has a significant financial interest in the medical profession rejecting ivermectin as an early treatment for COVID-19. [T]he U.S. government has agreed to pay [Merck] about $1.2 billion for 1.7 million courses of its experimental COVID-19 treatment, if it is proven to work in an ongoing large trial and authorized by U.S. regulators.”

Merck’s treatment is known as “molnupiravir,” and aims to stop COVID from progressing when given early in the course of disease. When Merck announced Oct. 1, that preliminary studies indicated molnupiravir reduced hospitalizations and deaths by half, the drug maker’s stock price immediately jumped to 12.3%.

“Thus, if low-cost ivermectin works better than, or even the same as molnupiravir, that could cost Merck billions of dollars,” Peterson wrote.

Pharma giant Merck is facing accusations of price gouging after it charged the U.S. more than $700 per patient for a taxpayer-funded coronavirus treatment that, according to research, costs just $17.74 to produce.https://t.co/BSYYnPmRBl

— Robert F. Kennedy Jr (@RobertKennedyJr) October 8, 2021

Peterson takes on science of hydroxychloroquine

Peterson said based on his review of the evidence, his office did not find clear and convin­cing evidence that would warrant disciplining physicians who prescribe hydroxychloroquine for the prevention or early treatment of COVID after first obtaining informed patient consent.

Peterson pointed to similar findings with hydroxychloroquine — a less toxic derivative of a medicine named chloroquine — widely used since it was approved by the FDA in 1955 for treatment of malaria.

Peterson noted that as early as 2004, a lab study revealed chloroquine was “an effective inhibitor of the replication of the severe acute respiratory syndrome coronavirus (SARS-CoV) in vitro” and should “be considered for immediate use in the prevention and treatment of SARS-CoV infections.”

In 2005, another study showed chloroquine had strong antiviral effects on SARS-CoV infection and was effective in preventing the spread of SARS-CoV in cell cultures.

Other studies showed hydroxychloroquine exhibited antiviral properties that can inhibit SARS-CoV-2 virus entry, transmission and replication, and contains anti-inflammatory properties that help regulate pro-inflammatory cytokines.

Peterson wrote, “many large observational studies suggest that hydroxychloroquine significantly reduces the risk of hospitalization and death when administered to ­particularly high-risk outpatients as part of early COVID-19 treatment.”

Peterson said the drug is considered to be so safe it can be prescribed for pregnant women, yet during the pandemic, the FDA raised questions about hydroxychloroquine and adverse cardiac events.

These concerns prompted one group of researchers to conduct a systematic review of the hydroxychloroquine safety literature pre-COVID. Their review indicated people taking hydroxychloroquine in appropriate doses “are at very low risk of experiencing cardiac [adverse events], particularly with short-term administration” of the drug.

Researchers noted COVID itself can cause cardiac problems, and there was no reason “to think the medication itself had changed after 70 years of widespread use,” Peterson wrote.

Peterson said one piece of key flawed data had substantially contributed to safety concerns surrounding the drug — the admittedly fraudulent Lancet study that falsely claimed hydroxychloroquine increased frequency of ventricular arrhythmias when used for treatment of COVID.

The findings were so startling that major drug trials involving hydroxychloroquine “were immediately halted” and the World Health Organization pressured countries like Indonesia that were widely using hydroxychloroquine to ban it. Some countries, including France, Italy and Belgium, stopped using it for COVID altogether.

Peterson wrote:

“The problem, however, is that the study was based on false data from a company named Surgisphere, whose founder and CEO Sapan Desai was a co-author on the published paper.

“The data were so obviously flawed that journalists and outside researchers began raising concerns within days of the paper’s publication. Even the Lancet’s editor in chief, Dr. Richard Horton, admitted that the paper was a fabrication, a monumental fraud and a shocking example of research misconduct in the middle of a global health emergency.”

Despite calls for the Lancet to provide a full expansion of what happened, the publication declined to provide details for the retraction.

As with ivermectin, the FDA and NIH adopted positions against the use of hydroxychloroquine for COVID — making assertions that were unsupported by data. The AMA, APhA and ASHP, which opposed ivermectin, also resisted hydroxychloroquine for the treatment of COVID.

By contrast, the Association of American Physicians and Surgeons, and other physician groups, support the use of both ivermectin and hydroxychloroquine as an early treatment option for COVID. Peterson cited an article co-authored by more than 50 doctors in Reviews in Cardiovascular Medicine who advocated an early treatment protocol that includes hydroxychloroquine as a key component.

Governing law allows physicians to prescribe ivermectin and hydroxychloroquine, AG says

Neb. Rev. Stat. § 38-179 generally defines unprofessional conduct as a “departure from or failure to conform to the standards of acceptable and prevailing practice of a profession or the ethics of the profession, regardless of whether a person, consumer or entity is injured, or conduct that is likely to deceive or defraud the public or is detrimental to the public interest.”

The regulation governing physicians states that unprofessional conduct includes:

“[c]onduct or practice outside the normal standard of care in the State of Nebraska which is or might be harmful or dangerous to the health of the patient or the public, not to include a single act of ordinary negligence.”

Peterson said healthcare providers do not violate the standard of care when they choose between two reasonable approaches to medicine.

“Regulations also indicate that physicians may utilize reasonable investigative or unproven therapies that reflect a reasonable approach to medicine so long as physicians obtain written informed patient consent,” Peterson wrote.

“Informed consent concerns a doctor’s duty to inform his or her patient, and it includes telling patients about the nature of the pertinent ailment or condition, the risks of the proposed treatment or procedure and the risks of any alternative methods of treatment, including the risks of failing to undergo any treatment at all.”

Peterson said this applies to prescribing medicine for purposes other than uses approved by the FDA, and that doing so falls within the standard of care repeatedly recognized by the courts.

Peterson said the U.S. Supreme Court has also affirmed that “off-label usage of medical devices” is an “accepted and necessary” practice, and the FDA has held the position for decades that “a physician may prescribe [a drug] for uses or in treatment regimens or patient populations that are not included in approved labeling.”

Peterson said the FDA has stated “healthcare providers generally may prescribe [a] drug for an unapproved use when they judge that it is medically appropriate for their patient, and nothing in the federal Food, Drug and Cosmetic Act (“FDCA”) limit[s] the manner in which a physician may use an approved drug.”

In a statement to KETV NewsWatch 7, Nebraska’s Department of Health and Human Services said:

“The Department of Health and Human Services appreciates the AG’s office delivering an opinion on this matter. The document is posted and available to medical providers as they determine appropriate course of treatment for their patients.”

© [10/18/21] Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our effort

 

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This shows you EXACTLY how the media & so called hollywood stars try to divide America, and most of you actually believe what they are saying. 

 

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Secret CIA Files Say Staffers Committed Sex Crimes Involving Children

Jason Leopold

Over the past 14 years, the Central Intelligence Agency has secretly amassed credible evidence that at least 10 of its employees and contractors committed sexual crimes involving children.

Though most of these cases were referred to US attorneys for prosecution, only one of the individuals was ever charged with a crime. Prosecutors sent the rest of the cases back to the CIA to handle internally, meaning few faced any consequences beyond the possible loss of their jobs and security clearances. That marks a striking deviation from how sex crimes involving children have been handled at other federal agencies such as the Department of Homeland Security and the Drug Enforcement Administration. CIA insiders say the agency resists prosecution of its staff for fear the cases will reveal state secrets.

The revelations are contained in hundreds of internal agency reports obtained by BuzzFeed News through Freedom of Information Act lawsuits.

 

One employee had sexual contact with a 2-year-old and a 6-year-old. He was fired. A second employee purchased three sexually explicit videos of young girls, filmed by their mothers. He resigned. A third employee estimated that he had viewed up to 1,400 sexually abusive images of children while on agency assignments. The records do not say what action, if any, the CIA took against him. A contractor who arranged for sex with an undercover FBI agent posing as a child had his contract revoked.

Only one of the individuals cited in these documents was charged with a crime. In that case, as in the only previously known case of a CIA staffer being charged with child sexual crimes, the employee was also under investigation for mishandling classified material.

The CIA did not answer detailed questions, saying only that the agency “takes all allegations of possible criminal misconduct committed by personnel seriously.”

A spokesperson for the Eastern District of Virginia, where many of the criminal referrals were sent, also did not answer detailed questions, saying the district “takes seriously its responsibility to hold accountable federal government employees who violate federal law within our jurisdiction.”

Four former officials who are familiar with how internal investigations work at intelligence agencies told BuzzFeed News there are many reasons that prosecutors might not pursue a criminal case. One of them, familiar with the workings of the CIA’s Office of the Inspector General, said the agency is concerned that in a criminal case, it could lose control of sensitive information.

The former official, who reviewed the declassified inspector general reports, characterized the concern from CIA lawyers as, “We can’t have these people testify, they may inadvertently be forced to disclose sources and methods.”

The official, who noted the agency has had a problem with child abuse images stretching back decades, said they understand the need to protect “sensitive and classified equities.” However, “for crimes of a certain class whether it’s an intelligence agency or not, you just have to figure out how to prosecute these people.”

Want to support more reporting like this? Become a BuzzFeed News member today.
Sexual crimes involving children, including the viewing of images of abuse, have been uncovered at other agencies that handle sensitive information. In a November 2009 report, the Department of Defense acknowledged that dozens of Pentagon staff members or contractors had such images. In 2014, the Inspector General of the Intelligence Community found that two officials from the National Reconnaissance Office, which oversees America’s spy satellites, acknowledged viewing images of child sexual abuse during polygraph examinations.

At a symposium in 2016, Daniel Payne, a top Pentagon security official, said that when workers’ computers were examined, “the amount of child porn I see is just unbelievable.”

The child abuse revelations are drawn from an unprecedented release of reports by the CIA’s Office of the Inspector General.

BuzzFeed News gained access to these documents after a decadelong pursuit, which included 13 public records requests and three separate Freedom of Information Act lawsuits.

Those requests, the earliest of which date back to 2012, were for investigations closed by the Office of the Inspector General, which acts independently of the agency to examine misconduct by employees or contractors.

New requests were filed each subsequent year. At first the CIA did not respond to the requests; then, it said it would take years to provide any documents. Those requests were followed in 2014, 2015, and 2020 by lawsuits, and the agency entered into negotiations about what documents to release. The coronavirus pandemic delayed the process by a year, but the agency finally began to release the documents in March and will release the final set in December.

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There is more than 1 movie going on ...  

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Yes, these clowns were also LIARS ..