Joe Rogan Know He Not Posed To Publicly Rub Horse Deworming Paste In His Hiney For Covid

Success against #COVID19 will likely require both vaccines & treatments. We’re pleased to share we’ve started a Phase 2/3 study of our oral antiviral candidate—specifically designed to combat SARS-CoV-2—in non-hospitalized, low-risk adults: https://t.co/su5VtfbWPX

— AlbertBourla (@AlbertBourla) September 1, 2021

msdnc |   Podcast host Joe Rogan told his millions of followers Wednesday that he has Covid-19 and used ivermectin, a drug typically used on livestock that health experts have urged the public to avoid.

Rogan, host of the immensely popular Spotify podcast "The Joe Rogan Experience," posted a video to Instagram explaining he tested positive for the coronavirus following his return from a live show Saturday. He said he had “fevers and sweats” and that he “threw the kitchen sink” at the illness.

His treatments included monoclonal antibodies and ivermectin, Rogan said. Ivermectin, which is not an anti-viral drug, is generally used to treat or prevent parasites in animals such as horses.

The U.S. Food and Drug Administration last month urged people to stop believing misinformation claiming the livestock treatment would help cure Covid, saying it saw multiple reports of patients who have been hospitalized after "self-medicating with ivermectin intended for horses.”

The agency clarified that FDA-approved ivermectin tablets meant to treat people with certain conditions caused by parasitic worms as well as topical formulations used for head lice and skin conditions like rosacea are different from the drug used on animals. Ivermectin tablets and topical formulations for humans have "very specific doses" that are significantly smaller than the doses meant for animals.

Patients who overdose with ivermectin can experience nausea, vomiting, diarrhea, low blood pressure, allergic reactions, dizziness, problems with balance, seizures, coma and even death, according to the FDA.

Rogan has more than 13 million followers on Instagram, and his podcast is the most-streamed program on Spotify.

 

This Is Not The First Time The Government Was Hand-in-Glove With The Drug Industry

C-19 is a disease of the eldery and obese. And the extremely unlucky healthy people who sometimes fall prey to a novel vascular endothelial proliferation vector in the body.
 
Does anybody really believe vaccine immunity is better than natural immunity? As a society the young developing natural immunity would have been the preferred public health strategy. The experimental mRNA therapeutics target a single antigenic point on the virus. ONE. The spike protein.
 
Natural immunity targets 28 antigenic proteins on the virus. Robust immunological memory produces a vast array of Defense in Depth.
 
From a scientific perspective the masking/vaxxing strategy is farcical and deserving of contempt. Many Public Health authorities apparently no longer believe in evolution via immunological memory and have become Flat Earthers.
 
Another common sense point, most miss. Where does the virus enter the human body? Through the respiratory tract. The nose and mouth. Where is the vaccine given? In the shoulder. On the other side of the moat. Sure some IgG through the lymphatic system probably progresses to the lungs. And then wanes over time.
 
But the defense against infection from respiratory viruses begins in the mucosal immunity. IgAs are produced here. They are much more important in preventing infections from C-19 and other respiratory illnesses than IgG which is blood based for the most part.
 
Guess what? Natural immunity from infection equals robust IgA response the second time the virus tries to enter the individual.
 
This would not be the first time the “government” hand in glove with the drug industry used its offices to circumvent FDA oversight and safety requirements, in order to establish a national for profit health care agenda. Prior example: life time use of hormone drug replacement therapy for women.
 
Following is a well-researched and documented study of the long-standing government recommendations and health information campaign advocating for the multi-billion dollar hormone replacement drug industry. This government agenda fell to “science” only when its decades long recommendations were finally put to a double blind, randomized study.
 
Ironically, the study was intended to support official FDA approval for lifetime drug use instead of short-term symptomatic use; only to learn the very drugs were causing the very problems they had been previously telling women they would avoid if they used these drugs, and plenty more.
 
The template is familiar- establish a public health social agenda using an unproven hypothesis, partner with a for-profit pharmaceutical company, and actively discredit all opposition:
 
The Greatest Experiment Ever Conducted on Women: Exploding the Estrogen Myth (Barbara Seamans – solid health researcher with footnotes)

Only NIH Approved Treatments Get The HHS Prep Act Liability Waiver

“Enacted in December 2005, the PREP Act authorizes the Secretary of HHS (Secretary) to issue a declaration (called a PREP Act declaration) that provides immunity from tort liability (except for willful misconduct) for claims of loss caused, arising out of, relating to, or resulting from administration or use of countermeasures to diseases, threats and conditions determined by the Secretary to constitute a present, or credible risk of a future public health emergency to entities and individuals involved in the development, manufacture, testing, distribution, administration, and use of such countermeasures.” (link)

 

A PREP Act declaration is specifically for the purpose of providing immunity from tort liability, and is different from, and not dependent on, other emergency declarations.

 

Under the HHS Notification, the PREP Act has been modified: “The amended Section VII adds that PREP Act liability protections also extend to Covered Persons for Recommended Activities that are related to any Covered Countermeasure that is:

 

1. licensed, approved, cleared, or authorized by the Food and Drug Administration (FDA) (or that is permitted to be used under an Investigational New Drug Application or an Investigational Device Exemption) under the Federal Food, Drug, and Cosmetic (FD&C) Act or Public Health Service (PHS) Act to treat, diagnose, cure, prevent, mitigate or limit the harm from COVID–19, or the transmission of SARS–CoV–2 or a virus mutating therefrom; (link)

 

The attachment of a liability or tort waiver to only cover FDA approved therapeutics likely explains a shift amid the medical community to stop patients treatment due to coverage restrictions on their malpractice insurance.  Additionally, Big Pharma -the group who controls NIH- wouldn’t make as much money if their mandatory vaccines had a less costly alternative.  So there’s that.

 

The PREP Act offers hospitals blanket financial liability protection in treating C19 patients only if the hospitals follow the approved protocol; if hospitals treat only with CDC, FDA approved countermeasures, i.e. NIH approved measures, they keep the liability shield. Any hospital deviating from the protocol loses the PREP Act C19 liability shield, it seems. Again, follow the money.

 

I can’t see any other reason hospitals would fight so hard to block dying patients last-chance medical requests for an FDA approved drug used off-label but not EUA’d for C19. It might explain the hospital’s use of the term “human guinea pig”.

 

This is from a brief outline of the current PREP Act applied to C19 treatments. Ivermectin is not a "covered countermeasure” by this definition.

 

“Fourth, the medical product at issue must be a covered countermeasure. The PREP Act specifies four types of covered countermeasures: (i) a qualified “pandemic or epidemic product”; (ii) a “security countermeasure”; (iii) a drug, biological product,or device that the U.S. Food and Drug Administration (FDA)has authorized for emergency use; and (iv) a “respiratory protective device” that is approved by the National Institute for Occupational Safety and Health (NIOSH).”

mRNA Neo-Vaccinoids A "Solution" In Search Of A Problem For Some Time Now...,

cepi  |  As the COVID-19 pandemic shows, in a world characterised by increasing population density, human mobility, and ecological change, emerging infectious diseases (EIDs) pose a real and growing threat to global health security.

Epidemic diseases affect us all. They do not respect borders.

The costs of EIDs are vast, in both human and economic terms. As well as the devastating death toll and disruption to societies, COVID-19 could cost the global economy $4.1 trillion, or almost 5% of global gross domestic product. Even small epidemics can cause tremendous economic disruption.

Vaccines are one of our most powerful tools in the fight to outsmart epidemics. The development of vaccines can help save lives, protect societies and restabilise economies.

The Coalition for Epidemic Preparedness Innovations’ (CEPI’s) mission is to stimulate and accelerate the development of vaccines against emerging infectious diseases and enable access to these vaccines for people during outbreaks.

Historically, vaccine development has been a long, risky, and costly endeavour. Planning for emerging infectious diseases is especially challenging: the market potential for vaccines against these diseases is limited and testing such vaccines is difficult.

We need a better system to speed the development of vaccines against emerging infectious diseases.

Events like the devastating 2014/15 outbreak of Ebola in West Africa—which killed more than 11,000 people and had an economic and social burden of over $53 billion—showed us that very few vaccines are ready to be used against these threats.

The world’s response to this crisis fell tragically short.  A vaccine that had been under development for more than a decade was not deployed until over a year into the epidemic. That vaccine was shown to be 100% effective, suggesting that much of the epidemic could have been prevented.

The creation of CEPI

The Coalition for Epidemic Preparedness Innovations (CEPI) was launched at Davos 2017 as the result of a consensus that a coordinated, international, and intergovernmental plan was needed to develop and deploy new vaccines to prevent future epidemics.

We are an innovative global partnership between public, private, philanthropic, and civil society organisations working to accelerate the development of vaccines against emerging infectious diseases and enable equitable access to these vaccines for affected populations during outbreaks.

Close collaboration with global partners are crucial to ensure the success of our work. Therefore, we will support coordinating activities to improve our collective response to epidemics, strengthening capacity in countries at risk, and advancing the regulatory science that governs product development.

CEPI 2017 Presentation to the WHO

 

Representatives Of Pollution And The Hurricane Of Sacrificial Violence

charleseisenstein |  Aside from criminals, who today serves as the representative of Smith’s “disorder,” “social chaos,” and “breakdown of values” that seem to be overtaking the world? For most of my life external enemies and a story-of-the-nation served to unify society: communism and the Soviet Union, Islamic terrorism, the mission to the moon, and the mythology of progress. Today the Soviet Union is long dead, terrorism has ceased to terrify, the moon is boring, and the mythology of progress is in terminal decline. Civil strife burns ever hotter, without the broad consensus necessary to transform it into unifying violence. For the right, it is Antifa, Black Lives Matter protesters, critical race theory academics, and undocumented immigrants that represent social chaos and the breakdown of values. For the left it is the Proud Boys, right wing militias, white supremacists, QAnon, the Capitol rioters, and the burgeoning new category of “domestic extremists.” And finally, defying left-right categorization is a promising new scapegoat class, the heretics of our time: the anti-vaxxers. As a readily identifiable subpopulation, they are ideal candidates for scapegoating.

It matters little whether any of these pose a real threat to society. As with the subjects of criminal justice, their guilt is irrelevant to the project of restoring order through blood sacrifice (or expulsion from the community by incarceration or, in more tepid but possibly prefigurative form, through “canceling”). All that is necessary is that the dehumanized class arouse the blind indignation and rage necessary to incite a paroxysm of unifying violence. More relevant to current times, this primal mob energy can be harnessed toward fascistic political ends. Totalitarians right and left invoke it directly when they speak of purges, ethnic cleansing, racial purity, and traitors in our midst.

Sacrificial subjects carry an association of pollution or contagion; their removal thus cleanses society. I know people in the alternative health field who are considered so unclean that if I so much as mention their names in a Tweet or Facebook post, the post may be deleted. Deletion is a certainty if I link to an article or interview with them. The public’s ready acceptance of such blatant censorship cannot be explained solely in terms of its believing the pretext of “controlling misinformation.” Unconsciously, the public recognizes and conforms to the age-old program of investing a pariah subclass with the symbology of pollution.

This program is well underway toward the Covid-unvaxxed, who are being portrayed as walking cesspools of germs who might contaminate the Sanctified Brethren (the vaccinated). My wife perused an acupuncture Facebook page today (which one would expect to be skeptical of mainstream medicine) where someone asked, “What is the word that comes to mind to describe unvaccinated people?” The responses were things like “filth,” “assholes,” and “death-eaters.” This is precisely the dehumanization necessary to prepare a class of people for cleansing.

The science behind this portrayal is dubious. Contrary to the association of the unvaccinated with public danger, some experts contend that it is the vaccinated that are more likely to drive mutant variants through selection pressure. Just as antibiotics result in higher mutation rates and adaptive evolution in bacteria, leading to antibiotic resistance, so may vaccines push viruses to mutate. (Hence the prospect of endless “boosters” against endless new variants.) This phenomenon has been studied for decades, as this article in my favorite math & science website, Quanta, describes. The mutated variants evade the vaccine-induced antibodies, in contrast to the robust immunity that, according to some scientists, those who have already been sick with Covid have to all variants (See this and this, more analysis here, compare to Dr. Fauci’s viewpoint.)

It is not my purpose here, however, to present a scientific case. My point is that those in the scientific and medical community who dissent from the demonization of the unvaxxed contend not only with opposing scientific views, but with ancient, powerful psycho-social forces. They can debate the science all they want, but they are up against something much bigger. Rwandan scientists could just as well have debated the precepts of Hutu Power for all the good that would have done. Perhaps the Nazi example is more apposite here, since the Nazis did invoke science in their extermination campaigns. Then as now, science was a cloak for something more primal. The hurricane of sacrificial violence easily swept aside the minority of German scientists who contested the science of eugenics, and it wasn’t because the dissidents were wrong.

The FDA Has No Credibility This Blogger Is Bound To Acknowledge...,

emilyposts |   A year ago, I would have tried to convince people that the FDA was the gold standard for COVID pharmaceuticals.

Now, I see that the agency needs to fail in order for it to be forced to make radical changes so that the public can trust that the label “approved by the FDA” means its safe.

Compounding the problem is that the FDA’s credibility gap has created a vacuum in which conspiracy theories and misinformation grow quickly. The result is many people don’t believe that the vaccine was actually approved. They don’t trust that it is safe to be vaccinated. They don’t even know who runs the FDA.

Had the FDA made the vaccines authorization and later approval process easy to understand by the public, this mess of vaccine distrust would not have happened. But the FDA refuses to work in public, deliver information in terms we all understand or even show their faces.

And all this could have been avoided if the FDA press office didn’t operate like the Cold War Kremlin. I tried to turn that ship around last year and was thrown overboard for the effort.

My FDA Assignment

I was hired at the FDA during the pandemic because the Commissioner, Dr. Stephen Hahn, needed someone skilled at handling the press in a crisis at the highest levels of government.

I was a spokesman for Capitol Hill leadership during 9/11 and a press secretary at the State Department during the wars in Iraq and Afghanistan.

The strategic communications needed for COVID was no different than the wars. The FDA needed to get as much information as allowed out to the public as quickly as possible and be accessible to reporters 24/7.

 

Two Senior FDA Biologics Reviewers Resign Over Pfizer Final Approval Fiasco

endpts  |   Two of the FDA’s most senior vaccine leaders are exiting from their positions, raising fresh questions about the Biden administration and the way that it’s sidelined the FDA.

Marion Gruber, director of the FDA’s Office of Vaccines Research & Review and 32-year veteran of the agency, will leave at the end of October, and OVRR deputy director Phil Krause, who’s been at FDA for more than a decade, will leave in November. The news, first reported by BioCentury, is a massive blow to confidence in the agency’s ability to regulate vaccines.

The bombshell announcement comes at a particularly crucial moment, as boosters and children’s shots are being weighed by the regulator. The departures also come as the administration has recently jumped ahead of the FDA’s reviews of booster shots, announcing that they might be available by the week of Sept. 20.

A former senior FDA leader told Endpoints that they’re departing because they’re frustrated that CDC and their ACIP committee are involved in decisions that they think should be up to the FDA. The former FDAer also said he’s heard they’re upset with CBER director Peter Marks for not insisting that those decisions should be kept inside FDA. What finally did it for them was the White House getting ahead of FDA on booster shots.

FDA’s former acting chief scientist Luciana Borio added on Twitter, “FDA is losing two giants who helped bring us many safe and effective vaccines over decades of public service.”

“These two are the leaders for Biologic (vaccine) review in the US. They have a great team, but these two are the true leaders of CBER. A huge global loss if they both leave,” Former BARDA director Rick Bright wrote, weighing in on the news. “Dr. Gruber is much more than the Director. She is a global leader. Visionary mastermind behind global clinical regulatory science for flu, Ebola, Mers, Zika, Sars-cov-2, many others.”

Grieving Military Parents Burn Old Cornpop...,

dailymail |  The mother of a Marine killed in the Kabul airport attack called President Joe Biden a 'dementia-riddent piece of crap' as the president meets with families of the 13 fallen service members on Sunday

'My son was one of the Marines that died yesterday,' Kathy McCollum said in a radio interview on Friday of her 20-year-old late son Rylee.

'[He was] getting ready to come home from freaking Jordan to be with his wife to watch the birth of his son,' McCollum said. 'And that feckless, dementia ridden piece of crap just sent my son to die.'

'I woke up at four'o'clock this morning to Marines at my door telling me my son was dead,' she said in the emotional account.

President Biden made an unannounced trip to Delaware on Sunday morning for a ceremony to honor the service members killed by an ISIS-K suicide bomber.

He stood in silence, his right hand to his chest, as a succession of flag draped transfer cases were carried past him from a C-17 Globemaster plane.

The 13 killed on Thursday were Navy corpsman Max Soviak, Army Staff Sergeant Ryan Knauss, and Marines Hunter Lopez, Rylee McCollum, David Lee Espinoza, Kareem Nikoui, Jared Schmitz, Daegan Page, Taylor Hoover, Humberto Sanchez, Johanny Rosario, Dylan Merola and Nicole Gee.

Their remains arrived at Dover Air Force Base, at 8am for a 'dignified transfer,; when fallen troops' return to American soil is marked by a solemn movement.

theconservativetreehouse |  Mrs. Shana Chappell is furious at the Biden administration, and now that we know the military was aware of the pending attack before it took place – the horrific event is even worse.  Mrs. Chappell’s voice cries out in anger and grief.   The incompetence and failed leadership in the Afghan withdrawal led to the death of her son, Kareem Nikoui.  Her Facebook and Instagram accounts have now been suspended.  

 

A Voluntary Product Of The System Publicly Threatening To Tear The System Down On Social Media?

Fist Tap Dale...,

Worse Than Horse Deworming Paste - CDC And Media Again Caught Prevaricating And Propagandizing

nakedcapitalism  |  Last Friday, the CDC published “Outbreak Associated with SARS-CoV-2 B.1.617.2 (Delta) Variant in an Elementary School — Marin County, California, May–June 2021” (“Outbreak”). This got a lot of play in the Northern California press, with a good deal of reporting done (or at least original stories written), because the study was led by Marin County Public Health, and they with other California epidemiologists and experts wrote the study up and then submitted it to the CDC, which accepted it. Good for them! However, there is a question “Outbreak” does not ask, and that the press did not ask. Carefully avoiding spoilers — though few NC readers will be surprised at the plot twist — I will first quote the “Outbreak” on the incident. Then I will switch into media critique mode, and present the headlines from Northern Califonia. After that, I will present the implications drawn from the outbreak by the press (which are more broad spectrum than the headlines). Finally, I will give the unasked question from “Outbreak” a thorough airing, and conclude.

Here is what “Outbreak” says in the “Investigation and Findings” section:

The outbreak location was an elementary school in Marin County, California… Each grade includes 20 to 25 students in single classrooms. Other than two teachers, one of whom was the index patient, all school staff members were vaccinated (verified in California’s Immunization Registry). The index patient became symptomatic on May 19 with nasal congestion and fatigue. This teacher reported attending social events during May 13–16 but did not report any known COVID-19 exposures and attributed symptoms to allergies. The teacher continued working during May 17–21, subsequently experiencing cough, subjective fever, and headache. The school required teachers and students to mask while indoors; interviews with parents of infected students suggested that students’ adherence to masking and distancing guidelines in line with CDC recommendations (3) was high in class. However, the teacher was reportedly unmasked on occasions when reading aloud in class. On May 23, the teacher notified the school that they received a positive result for a SARS-CoV-2 test performed on May 21 and self-isolated until May 30. The teacher did not receive a second COVID-19 test, but reported fully recovering during isolation.

The index patient’s students began experiencing symptoms on May 22. During May 23–26, among 24 students in this grade, 22 were tested…. Twelve (55%) of the 22 students received a positive test result, including eight who experienced symptom onset during May 22–26. Throughout this period, all desks were separated by 6 ft. Students were seated in five rows; the attack rate in the two rows seated closest to the teacher’s desk was 80% (eight of 10) and was 28% (four of 14) in the three back rows…

On May 22, students in a another classroom, who differed in age by 3 years from the students in the class with the index case and who were also ineligible for vaccination began to experience symptoms. The two classrooms were separated by a large outdoor courtyard with lunch tables that were blocked off from use with yellow tape. All classrooms had portable high-efficiency particulate air filters and doors and windows were left open. Fourteen of 18 students in this separate grade received testing; six tests had positive results. Investigation revealed that one student in this grade hosted a sleepover on May 21 with two classmates from the same grade. All three of these students experienced symptoms after the sleepover and received positive SARS-CoV-2 test results. Among infected students in this class, test dates ranged from May 24 to June 1; symptom onset occurred during May 22–31.

So that’s the outbreak. Here are the headlines:

• CDC: Unvaccinated Marin County teacher caused big COVID-19 outbreak in school San Francisco Chronicle
• CDC study finds unvaccinated Marin Co. teacher infected 22 elementary school students with COVID ABC7
• CDC report confirms unvaccinated Marin County teacher was source of Delta variant outbreak KTVU
• CDC study shows unvaccinated teacher started Delta COVID outbreak at Marin school KSBW
• One Unvaccinated Teacher In Marin School Seeded COVID Outbreak That Infected Over a Dozen Students, Their Siblings, and Parents SFist
• How 1 unvaccinated Marin County teacher started a delta variant outbreak: CDC study KRON4

There is a unanimity of opinion by the headline-writing editors that the source of the problem was the index case: the unvaccinated teacher. Indeed, that’s without justification — that is, is not only a matter of aghastitude — given the “Implications for Public Health Practice” in the Summary section of “Outbreak”:

Vaccines are effective against the Delta variant, but transmission risk remains elevated among unvaccinated persons in schools. In addition to vaccination, strict adherence to multiple nonpharmaceutical prevention strategies, including masking, are important to ensure safe school instruction.

(I presume the Summary is tacked on to the submitted study by CDC.) Now let’s turn to the bodies of the stories, where there is a broader spectrum of opinion than in the headlines.

The Commission on Information Disorder?

Harpers |  In the beginning, there were ABC, NBC, and CBS, and they were good. Midcentury American man could come home after eight hours of work and turn on his television and know where he stood in relation to his wife, and his children, and his neighbors, and his town, and his country, and his world. And that was good. Or he could open the local paper in the morning in the ritual fashion, taking his civic communion with his coffee, and know that identical scenes were unfolding in households across the country.

Over frequencies our American never tuned in to, red-baiting, ultra-right-wing radio preachers hyperventilated to millions. In magazines and books he didn’t read, elites fretted at great length about the dislocating effects of television. And for people who didn’t look like him, the media had hardly anything to say at all. But our man lived in an Eden, not because it was unspoiled, but because he hadn’t considered any other state of affairs. For him, information was in its right—that is to say, unquestioned—place. And that was good, too.

Today, we are lapsed. We understand the media through a metaphor—“the information ecosystem”—which suggests to the American subject that she occupies a hopelessly denatured habitat. Every time she logs on to Facebook or YouTube or Twitter, she encounters the toxic byproducts of modernity as fast as her fingers can scroll. Here is hate speech, foreign interference, and trolling; there are lies about the sizes of inauguration crowds, the origins of pandemics, and the outcomes of elections.

She looks out at her fellow citizens and sees them as contaminated, like tufted coastal animals after an oil spill, with “disinformation” and “misinformation.” She can’t quite define these terms, but she feels that they define the world, online and, increasingly, off.

Everyone scrounges this wasteland for tainted morsels of content, and it’s impossible to know exactly what anyone else has found, in what condition, and in what order. Nevertheless, our American is sure that what her fellow citizens are reading and watching is bad. According to a 2019 Pew survey, half of Americans think that “made-up news/info” is “a very big problem in the country today,” about on par with the “U.S. political system,” the “gap between rich and poor,” and “violent crime.” But she is most worried about disinformation, because it seems so new, and because so new, so isolable, and because so isolable, so fixable. It has something to do, she knows, with the algorithm.

What is to be done with all the bad content? In March, the Aspen Institute announced that it would convene an exquisitely nonpartisan Commission on Information Disorder, co-chaired by Katie Couric, which would “deliver recommendations for how the country can respond to this modern-day crisis of faith in key institutions.” The fifteen commissioners include Yasmin Green, the director of research and development for Jigsaw, a technology incubator within Google that “explores threats to open societies”; Garry Kasparov, the chess champion and Kremlin critic; Alex Stamos, formerly Facebook’s chief security officer and now the director of the Stanford Internet Observatory; Kathryn Murdoch, Rupert Murdoch’s estranged daughter-in-law; and Prince Harry, Prince Charles’s estranged son. Among the commission’s goals is to determine “how government, private industry, and civil society can work together . . . to engage disaffected populations who have lost faith in evidence-based reality,” faith being a well-known prerequisite for evidence-based reality.

The Commission on Information Disorder is the latest (and most creepily named) addition to a new field of knowledge production that emerged during the Trump years at the juncture of media, academia, and policy research: Big Disinfo. A kind of EPA for content, it seeks to expose the spread of various sorts of “toxicity” on social-media platforms, the downstream effects of this spread, and the platforms’ clumsy, dishonest, and half-hearted attempts to halt it. As an environmental cleanup project, it presumes a harm model of content consumption. Just as, say, smoking causes cancer, consuming bad information must cause changes in belief or behavior that are bad, by some standard. Otherwise, why care what people read and watch?

Big Disinfo has found energetic support from the highest echelons of the American political center, which has been warning of an existential content crisis more or less constantly since the 2016 election. To take only the most recent example: in May, Hillary Clinton told the former Tory leader Lord Hague that “there must be a reckoning by the tech companies for the role that they play in undermining the information ecosystem that is absolutely essential for the functioning of any democracy.”

NIH Being Effectively Sued For Deception With Regard To Ivermectin Efficacy...,

Trialsite  |  On August 25, NIH appeared in conference in federal court in the District of New Jersey. The purpose of the appearance was for resolution of Jin-Pyong Peter Yim v National Institutes of Health and for scheduling of “motion practice”, if necessary. I am the plaintiff in the case. Beneath the legal formalities, the case could reveal that NIH deceived the nation on a treatment for COVID-19.

NIH is alleged to have violated the Freedom of Information Act. NIH failed to respond to a document request made on January 28, 2021:

“All updates to the Coronavirus Disease 2019 (COVID-19) Treatment Guidelines that were endorsed by a vote of the Panel. (Date Range for Record Search: From 01/01/2021 To 01/28/2021)”

The purpose of the FOIA request was not to obtain the document. Rather, it was to know if a vote was held to endorse the NIH recommendation on ivermectin. NIH violated FOIA because it did not respond within the time defined by statute. A complaint was filed against the NIH on March 26, 2021 to appeal the non-response. NIH answered the complaint on June 30. The answer included an exhibit and testimony.

NIH was represented by Margaret Ann Mahoney. She stated that NIH had responded to the FOIA request. She was referring to the NIH FOIA response from April 23:

“You requested all updates to the Coronavirus Disease 2019 (COVID-19) Treatment Guidelines that were endorsed by a vote of the Panel (Date range for record search from 01/01/2021 to 01/28/2021). All approved updates to the guidelines are posted online and can be found here. The documents posted on this website respond to your request in full.”

I requested a change to the NIH response. The NIH response is ambiguous as to whether the requested document exists. I provided a URL that refers to a single document. I requested that that URL be given in the NIH FOIA response if that recommendation was endorsed by a vote.

The conference was presided over by Judge Lois H. Goodman. She gave her opinion following discussion between the plaintiff and defendant. She expressed skepticism of the legal basis for the complaint. However, she urged further negotiation and allowed for “motion practice” if no agreement was reached. Her concluding remarks are here.

Following the conference, Judge Goodman also issued the following order:

“TEXT ORDER directing parties to confer to attempt resolution to this dispute. Parties to report to the Court as to the results of those efforts to resolve by 9/8/2021. If, matter cannot be resolved, dispositive motions to be filed by 9/24/2021 and to be returnable on 10/18/2021. Ms. Mahoney is directed to provide pro se plaintiff with a copy of this text order. So Ordered by Magistrate Judge Lois H. Goodman on 8/26/2021 .”

To Deny Natural Immunity Is To Deny Science...,

alexberenson |  The question I get more than any other:

I had Covid. I had an antibody test to prove it. Am I protected (and do I need to get the vaccine)?

Let me start with the usual disclaimer: THIS IS NOT MEDICAL ADVICE. I AM NOT A PHYSICIAN.

But the answer is now increasingly clear: natural immunity from Covid following infection and recovery is HIGHLY protective against future Covid infections. Rates of reinfection are very low.

Perhaps natural immunity eventually wanes, but we don’t know when. In fact, a little-noticed paper from June suggests it may actually strengthen for at least a year - and provide plenty of protection from Delta and other variants.

I am not going into the problems with vaccine-generated protection today or with our political unwillingness to recognize natural immunity. (Remember, GOOD NEWS - we could all use it).

Let’s just look instead at why natural immunity works so well.

You immune response comes in two forms: “humoral” and “cellular.”

When you are infected with Sars-Cov-2, your body’s “B-cells” - part of the immune system - quickly pour out “antibodies.” These antibodies attack the viral particles circulating in your blood and other fluids, hoping to keep the virus from entering your cells and replicating itself.

This is humoral immunity. Your B-cells make antibodies in many different shapes. Some are better at sticking to the virus. Scientists call these “neutralizing” antibodies because they neutralize the “antigen,” the foreign body attacking you, keeping it from entering your cells.

Amazingly, your B-cells quickly figure out which antibodies neutralize most effectively and make more of them, while cutting back on those that don’t work.

At the same time, another part of the immune system - killer or CD8 T-cells - attacks cells that the virus has already infected. You destroy your own cells to prevent the virus from using them to make more copies of itself. This is cellular immunity.

For a few days after you are infected, your immune system is in a race with the virus. If you win the race, defeat the virus, and recover - as the vast majority of people infected with Sars-Cov-2 do - within a week or two you should have no measurable levels of virus in your body.

Why Don't Public Health Officials "Remember" What Happened With Polio Vaccine?

americanthinker |  Prior to the 1950s, paralytic polio was a scourge.  FDR was crippled from it while in his 30s, the March of Dimes was started to combat it, and photos of rows and rows of children in iron lungs were common in the media.  From this situation, vaccines were developed to combat the disease.

Polio is caused by one of three types of poliovirus that can cause paralysis and death.  In the 1950s, two vaccines were independently developed to combat it, one by Jonas Salk and the other by Albert Sabin.  Polio was eradicated, and today those vaccines are thought of as miracle drugs.  But were they?

In the early 1950s, Salk was the first to come out with a vaccine.  His was designed to treat all three polio viruses at once.  His approach seemed basic enough.  It was to grow polioviruses in the lab, kill them, and then inject healthy children with the dead viruses.  The idea was that the dead viruses could not reproduce, so they could not harm the children.  The children's immune system, however, would detect the injected viruses and produce effective antibodies against them, thus creating immunity against polio.

Just prior to beginning mass inoculations, samples of the Salk vaccine were sent to the National Institutes of Health (NIH) for safety testing. 

There, when bacteriologist Dr. Bernice Eddy injected the vaccine into her monkeys, some of them fell down paralyzed.  She concluded that the virus was not entirely dead as promised.  Instead, the virus was active and could reproduce in its host.  Eddy sounded the alarm and presented her findings.  A debate ensued in the corridors of power.  Advocates for caution were overruled, and the mass inoculation proceeded on schedule. 

The inoculation of children began in 1955.  Within days, some injected children were coming down with polio.  Some were even spreading the disease to family members.  Subsequent investigations determined that the vaccine had caused 40,000 cases of polio, leaving 200 children with varying degrees of paralysis and ten dead.  Alton Ochsner, a professor of surgery at Tulane Medical School, was such a strong proponent of proceeding with the inoculation program that he gave vaccine injections to his grandchildren to prove that it was safe.  Ochsner's grandson died from polio a few months later, and his granddaughter contracted polio but survived. 

This fiasco has become known as the Cutter incident.  It's named after the manufacturer of the vaccine.  The vaccine was recalled and retested for safety, but the damage had already been done in the mind of the public.

Fugg Around With Sheeple Quantum Biology, But You Not Gonna Phug With Mine...,

medical-net  |  Quantum biology is an emerging field of science, established in the 1920s, which looks at whether the subatomic world of quantum mechanics plays a role in living cells. Quantum mechanics is an interdisciplinary field by nature, bringing together nuclear physicists, biochemists and molecular biologists.

In a research paper published by the journal Physical Chemistry Chemical Physics, a team from Surrey's Leverhulme Quantum Biology Doctoral Training Centre used state-of-the-art computer simulations and quantum mechanical methods to determine the role proton tunneling, a purely quantum phenomenon, plays in spontaneous mutations inside DNA.

Proton tunneling involves the spontaneous disappearance of a proton from one location and the same proton's re-appearance nearby.

The research team found that atoms of hydrogen, which are very light, provide the bonds that hold the two strands of the DNA's double helix together and can, under certain conditions, behave like spread-out waves that can exist in multiple locations at once, thanks to proton tunneling. This leads to these atoms occasionally being found on the wrong strand of DNA, leading to mutations.

Although these mutations' lifetime is short, the team from Surrey has revealed that they can still survive the DNA replication mechanism inside cells and could potentially have health consequences.

Dr Marco Sacchi, the project lead and Royal Society University Research Fellow at the University of Surrey, said: "Many have long suspected that the quantum world - which is weird, counter-intuitive and wonderful - plays a role in life as we know it. While the idea that something can be present in two places at the same time might be absurd to many of us, this happens all the time in the quantum world, and our study confirms that quantum tunneling also happens in DNA at room temperature."

There is still a long and exciting road ahead of us to understand how biological processes work on the subatomic level, but our study - and countless others over the recent years - have confirmed quantum mechanics are at play. In the future, we are hoping to investigate how tautomers produced by quantum tunneling can propagate and generate genetic mutations."

Louie Slocombe, PhD Student, Leverhulme Quantum Biology Doctoral Training Centre and Study Co-Author

Jim Al-Khalili, a co-author of the study and Co-Director of the Leverhulme Quantum Biology Doctoral Training Centre at the University of Surrey, said: "It has been thrilling to work with this group of young, diverse and talented thinkers - made up of a broad coalition of the scientific world. This work cements quantum biology as the most exciting field of scientific research in the 21st century."

mRNA Neo-Vaccinoids Are An ABOMINATION To The Root Of Life Itself

discovermagazine |  With photosynthesis, scientists show for the first time that there are quantum effects in living systems. This could lead to better solar panels, energy storage or even quantum computers. (Credit: Shutterstock) We all probably learned about photosynthesis, how plants turn sunlight into energy, in school. It might seem, therefore, that we figured out this bit of the world. But scientists are still learning new things about even the most basic stuff (see also the sun and moon), and photosynthesis is no different. In particular, according to a study released Monday in Nature Chemistry, an international team of scientists showed that molecules involved in photosynthesis display quantum mechanical behavior. Even though we’d suspected as much before, this is the first time we’ve seen quantum effects in living systems. Not only will it help us better understand plants, sunlight and everything in between, but it could also mean cool new tech in the future.

The Quantum Conundrum

First, let’s back up. While photosynthesis may be taught in classrooms the world over, quantum mechanics is a bit less popular, in part because it’s so weird. Nobel Prize-winning quantum physicist Richard Feynman once said, "I think I can safely say that nobody understands quantum mechanics." It’s so impenetrable to non-experts that the same metaphors come up whenever someone tries to explain it. You might have heard of Schrödinger's Cat, which is both alive and dead at the same time thanks to quantum weirdness — in particular, because electrons can be in two states at the same time. It’s only when we observe the system that the weirdness collapses and reality “picks” one state: the cat’s actually alive (or dead), the electron’s actually at this end of the room (or that end). But quantum effects are typically limited to the very small, and only really observable in perfect, laboratory conditions. A living being, with its wet, messy systems, would be a tough place to find some quantum weirdness lurking — and yet we have. 

Molecular Madness

Scientists zoomed in on the Fenna-Matthews-Olson (FMO) complex, a key component of green sulfur bacteria's machinery for photosynthesis. It’s been a historical favorite for such research because we’ve long known its structure and it's fairly easy to work with. Previous experiments had seemed to show light-sensitive molecules in this area in two different states at the same time — that’s quantum weirdness — but the effect lasted more than 1 picosecond, which is much longer than expected. This new study shows that it was really just regular vibrations in the molecules, nothing quantum about it. But researchers have been excited about the possibilities of quantum biology for years, so having disproved the earlier experiments, the authors wanted to find some new evidence of their own. “We wondered if we might be able to observe that Schrödinger cat situation,” says co-author Thomas la Cour Jansen in a press release. And observe it they did! With a technique called two-dimensional electronic spectroscopy, researchers saw molecules in simultaneous excited states — quantum weirdness akin to a cat being alive and dead at the same time. What’s more, the effect lasted exactly as long as theories predicted it, suggesting this evidence of quantum biology will last. As the authors succinctly put it, “Thus, our measurements provide an unambiguous experimental observation of excited-state vibronic coherence in the FMO complex.” What could be simpler? The results shed light (haha) on how to harvest energy from light, and the team thinks they’re “generally applicable” to a variety of systems, living and non-living alike. This means it could result in engineering benefits such as better solar panels, energy storage or even quantum computers. And, of course, updated textbooks for tomorrow’s lessons on photosynthesis.

 

I Don't Think Of Quantum Biology As A Metaphor...,

quantamagazine  |   It’s not surprising that quantum physics has a reputation for being weird and counterintuitive. The world we’re living in sure doesn’t feel quantum mechanical. And until the 20th century, everyone assumed that the classical laws of physics devised by Isaac Newton and others — according to which objects have well-defined positions and properties at all times — would work at every scale. But Max Planck, Albert Einstein, Niels Bohr and their contemporaries discovered that down among atoms and subatomic particles, this concreteness dissolves into a soup of possibilities. An atom typically can’t be assigned a definite position, for example — we can merely calculate the probability of finding it in various places. The vexing question then becomes: How do quantum probabilities coalesce into the sharp focus of the classical world?

Physicists sometimes talk about this changeover as the “quantum-classical transition.” But in fact there’s no reason to think that the large and the small have fundamentally different rules, or that there’s a sudden switch between them. Over the past several decades, researchers have achieved a greater understanding of how quantum mechanics inevitably becomes classical mechanics through an interaction between a particle or other microscopic system and its surrounding environment.

One of the most remarkable ideas in this theoretical framework is that the definite properties of objects that we associate with classical physics — position and speed, say — are selected from a menu of quantum possibilities in a process loosely analogous to natural selection in evolution: The properties that survive are in some sense the “fittest.” As in natural selection, the survivors are those that make the most copies of themselves. This means that many independent observers can make measurements of a quantum system and agree on the outcome — a hallmark of classical behavior.

This idea, called quantum Darwinism (QD), explains a lot about why we experience the world the way we do rather than in the peculiar way it manifests at the scale of atoms and fundamental particles. Although aspects of the puzzle remain unresolved, QD helps heal the apparent rift between quantum and classical physics.

Only recently, however, has quantum Darwinism been put to the experimental test. Three research groups, working independently in Italy, China and Germany, have looked for the telltale signature of the natural selection process by which information about a quantum system gets repeatedly imprinted on various controlled environments. These tests are rudimentary, and experts say there’s still much more to be done before we can feel sure that QD provides the right picture of how our concrete reality condenses from the multiple options that quantum mechanics offers. Yet so far, the theory checks out.

 

 

Dr. Christina Parks And Virginia Stoner Swing The Scientific SledgeHammer On The mRNA Neo-Vaccinoids

virginiastoner | Vaccine dangers hiding in plain sight FACT: There has been a massive increase in deaths reported to the Vaccine Adverse Event Reporting System (VAERS) this year. That’s not a ‘conspiracy theory’, that’s an indisputable fact. You can try to explain it or justify it, or even argue it doesn’t matter, but you can’t deny it.

We’re not talking about a modest increase in death reports, something we might chat about in concerned voices over Chai tea and bagels at a company mixer. We’re talking about a huge and unprecedented increase—so massive that in the last 4 months alone, VAERS has received over 40% of all death reports it has ever received in its entire 30+year history. So massive it’s literally “off the chart.” The first chart in the pair below shows VAERS death reports from 2014 thru 2020. If you tried to add the 2021 data to it, it would be way, way off the chart. The second chart shows how much detail was lost when the 2021 data was squeezed in.

The pair of charts below are another illustration. Notice all age groups had an increase in death reports from the COVID-19 vaccines—with both the 18-64 and 65+ age groups experiencing a dramatic “off the chart” increase.

The increase in VAERS death reports is not due to more vaccination Even with the COVID-19 shots, the estimated total vaccines administered so far this year is less than the yearly average–because we are only a quarter of the way through this year. No doubt the vaccine count will climb much higher by the end of this year, but it’s not the reason for the massive increase in VAERS death reports over the last 4 months. The following chart compares estimates of vaccines administered with deaths reported to VAERS, separating COVID-19 vaccines from other vaccines. The rate of reported deaths for other vaccines looks fairly normal; the massive increase is mainly from the COVID-19 vaccines.

There are many notes at the end of this paper about how the vaccine data was estimated, and where the data for these charts was obtained, along with the data table.

But, But.., Ivermectin Formulated And Prescribed For Humans Is As Cheap And Harmless As Aspirin....,

abcnews  |  Washington County's sheriff confirmed Tuesday night that jail inmates had been prescribed ivermectin, but did not say how many. It wasn't clear if all the inmates who were prescribed the medication had tested positive for COVID-19.

“There is an open investigation and we can’t comment on it right now," Embry told The Associated Press.

Dr. Rob Karas, the jail's physician, has said no inmates were forced to take the drug.

The U.S. Food and Drug Administration has approved ivermectin for use by people and animals for some parasitic worms, head lice and skin conditions. The FDA has not approved its use in treating or preventing COVID-19 in humans. According to the FDA, side effects for the drug include skin rash, nausea and vomiting.

“Using any treatment for COVID-19 that’s not approved or authorized by the FDA, unless part of a clinical trial, can cause serious harm,” the FDA said in a warning about the drug.

Embry declined to say who was the target of the board's investigation. The board has authority over physicians, but not jail facilities.

Sheriff Tim Helder did not return a message Thursday, and a spokesperson for the sheriff's office did not immediately respond to questions about the drug's use.

In a lengthy statement released to the AP Thursday, Karas defended the use of ivermectin to treat COVID-19. Karas said he has prescribed it to inmates and patients at his clinics who are significantly sick with COVID-19 since late 2020. He did not respond to questions about the investigation and the number of inmates who have have been prescribed the drug.

“I do not have the luxury of conducting my own clinical trial or study and am not attempting to do so," Karas wrote. “I am on the front line of trying to prevent death and serious illness."

The Northwest Arkansas Democrat-Gazette reported that the sheriff's office said Helder had learned of the drug's use at the jail on Tuesday. In a July 20 email to Helder, Karas recommended the sheriff's staff take it as a preventive measure against COVID-19 but did not mention its use on inmates. Karas has said he's taken the drug, as have members of his family.

Arkansas Karenwaffen Justice Of The Peace BIG MAD About MD Prescribing Ivermectin For Covid

dailymail  |  A jail doctor in Washington County, Arkansas, has been using an animal deworming drug to treat inmates with Covid-19 even though the US Food and Drug Administration (FDA) has specifically warned against it.

Ivermectin is often used as a dewormer in animals including cows and horses, and is not recommended for treating the virus. The FDA said it 'can cause serious harm'.

During a finance and budget committee meeting for Washington County on Tuesday night the jail's physician Dr Rob Karas asked for a 10 per cent increase in the medical services contract, even after the county sheriff confirmed that the jail health provider had been prescribing the drug. 

Dr Karas has faced calls to resign over the revelation.  

County-elected Justice of the Peace Eva Madison brought the issue back up towards the end of the meeting after jail officials presented their 2022 budget. 'I learned today that Dr Karas is giving ivermectin - cow dewormer - to the inmates at the jail,' she said.

Madison told members of the Washington County quorum court - the county's governing body - that a jail official and county employee, who asked to stay anonymous, told her they had been sent to the jail's clinic to get tested for Covid-19. 

When the unidentified person tested negative they told Madison they were given a $76 prescription for ivermectin, as reported by CBS News.

'They were concerned about the prescription, asked their primary care physician about it and the doctor told him to 'throw that in the trash,' she said.

'(The person) tested negative, was given a prescription for ivermectin, was told to go to Dr Karas's pharmacy just off campus to have it filled,' Madison told the committee. 

She added: 'He's out $76 because of Dr Karas prescribing dewormer to a county employee for treatment of a condition that he didn't have.

'The employee had the good fortune to have a physician that he could go to and ask for a second opinion. Our inmates do not have that choice.'

Washington County Sheriff Tim Helder did not say how many inmates at the 710-bed facility had been given ivermectin and defended Dr Karas, who has been prescribing the medication.