The Most Revolutionary Act

Uncensored updates on world events, economics, the environment and medicine

The Most Revolutionary Act
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About stuartbramhall

Retired child and adolescent psychiatrist and American expatriate in New Zealand. In 2002, I made the difficult decision to close my 25-year Seattle practice after 15 years of covert FBI harassment. I describe the unrelenting phone harassment, illegal break-ins and six attempts on my life in my 2010 book The Most Revolutionary Act: Memoir of an American Refugee.

22 Countries Successfully Used Ivermectin To Treat Covid 19; Why Was It Banned in the US?

Updated 2022 Article

“Twenty countries are using Ivermectin to treat Covid-19. They include Mexico, Guatemala, Argentina, Brazil, Bolivia, Slovakia, the Czech Republic, Portugal, Nigeria, and Egypt. In South Africa doctors are allowed to prescribe Ivermectin, but it is not being rolled out everywhere and in hospitals and clinics.  According to Jackie Stone, a doctor in Zimbabwe, since January – when Ivermectin began to be used – it has cut COVID hospital admissions and deaths over 70%.

“The death rate rose sharply in January and peaked on the 25th at 70 deaths per day. Official authorisation for the use of Ivermectin was granted on 26th January. Just one month later, on 26th February, the COVID death rate had fallen to zero”.

A meta-analysis gold standard review of 24 randomised trials conducted in 15 countries among more than 3400 people worldwide of clinical trials – just released by the BIRD group in the UK – showed that deaths are dramatically reduced when Ivermectin is administered. Published in the American Journal of Therapeutics the most rigorous statistical standards were applied by world-leading biostatistician, Mr Andrew Bryant, and medical doctor and researcher Dr Tess Lawrie. The results concluded that Ivermectin has an over 70% success in preventing deaths in hospitalised patients.

A plea to allow the use of Ivermectin as Covid-19 treatment delivered to Ramaphosa’s house – BizNews.com

Via https://agrdailynews.com/2024/05/22/a-plea-to-allow-the-use-of-ivermectin-as-covid-19-treatment-delivered-to-ramaphosas-house/

Childhood Vaccine Schedule Led to ‘Greatest Decline in Public Health in Human History’

childhood vaccine schedule

Dr Mercola

Story at-a-glance

  • A U.S. Senate roundtable discussion, hosted by Sen. Ron Johnson, tackled a taboo topic — why public health agencies have not studied the health outcomes of vaccinated versus unvaccinated children
  • In 1962, children received just five vaccine doses. As of 2023, children up to age 18 receive 73 doses of 16 different vaccines; the cumulative effects of this childhood vaccine schedule have never been tested
  • Research shows vaccinated children experienced significantly higher instances of various health issues, including allergies, asthma, behavioral issues and gastroenteritis
  • The 1986 National Childhood Vaccine Injury Act requires the U.S. Department of Health and Human Services (HHS) to report on vaccine safety every two years, but the agency has “never submitted a vaccine safety report to Congress”
  • Health agencies have data on health outcomes for vaccinated and unvaccinated children, but they refuse to make it public, likely due to financial conflicts of interest

A U.S. Senate roundtable discussion, hosted by Sen. Ron Johnson, tackled a taboo topic — why public health agencies have not studied the health outcomes of vaccinated versus unvaccinated children — and have refused to make data on the topic available to the public.1

“They do not publish the results [or] let any independent scientist in to look at that information,” Brian Hooker, chief scientific officer for Children’s Health Defense, said. “They refuse to publish the results and they really know why. It’s because the bloated vaccination schedule is responsible and is, I would say, in part responsible for the epidemic of chronic disorders that we see in children in the U.S.”2

In 1962, children received just five vaccine doses. As of 2023, children up to age 18 receive 73 doses of 16 different vaccines. The cumulative effects of this childhood vaccine schedule have never been tested.

Explosion of Childhood Vaccines Led to ‘Greatest Decline in Public Health in Human History’

Del Bigtree, CEO of the Informed Consent Action Network (ICAN), referenced the significant increase in chronic illnesses that’s risen along with the number of childhood vaccines.

“In the 1980s, when we were giving 11 doses of about three vaccines, the chronic illness rate, which includes neurological and autoimmune disease, was 12.8%. Once we passed the 1986 [National Childhood Vaccine Injury] Act and we had the gold rush of vaccines explode … the chronic illness rate, neurological and autoimmune disease, skyrocket[ed] to 54%,” he said.3

However, that was in 2011 to 2012 — and might be even worse today. “We have no idea since then how bad this has gotten. But what you were looking at right there is the greatest decline in public health in human history,” Bigtree noted.4 He added:5

“None of the 14 routine vaccines on the CDC’s recommended schedule … was ever put through long-term double-blind placebo-based safety trials prior to licensure. Since this type of trial is really the only way to establish that a pharmaceutical product is safe, it is misinformation to state that the vaccines are safe.”

On the contrary, a number of studies suggest that unvaccinated children may be healthier than those who are vaxxed.

Vaccinated Children Have Higher Rates of Asthma, Neurodevelopmental Disorders and More

Dr. Paul Thomas, whose medical license was suspended due to his advocacy for informed consent regarding vaccinations, along with James Lyons-Weiler from the Institute for Pure and Applied Knowledge (IPAK), conducted a study comparing the health of vaccinated and unvaccinated children.6

Their findings revealed that vaccinated children experienced significantly higher instances of various health issues, including:7

Asthma Allergies
Eczema Sinusitis
Gastroenteritis Respiratory infections
Middle ear infection Conjunctivitis
Breathing issues Behavioral issues

Notably, among the 561 unvaccinated children, none were diagnosed with attention deficit hyperactivity disorder (ADHD), whereas 0.063% of children who had received some or all recommended vaccinations were diagnosed with ADHD.

“The implications of these results for the net public health effects of whole-population vaccination and with respect for informed consent on human health are compelling,” they wrote.8 The study also points out that the rate of autism spectrum disorder in their practice was half that of the U.S. national average (0.84% versus 1.69%). The rate of ADHD in the practice was also about half the national rate.

According to the authors, “The data indicate that unvaccinated children in the practice are not unhealthier than the vaccinated and indeed the overall results may indicate that the unvaccinated pediatric patients in this practice are healthier overall than the vaccinated.”9

At the roundtable, Hooker added, “‘When you look at developmental delays, when you look at asthma, when you look at ear infections, when you look at allergies, when you look at ADD [attention deficit disorder], ADHD, autism,’ unvaccinated children fare ‘way better.’”10

Aluminum Toxicity Alone Is a Problem

There are multiple mechanisms of potential harm when it comes to vaccination. One of them involves aluminum, the most commonly used vaccine adjuvant.11 A demonstrated neurotoxin, aluminum is added to certain vaccines to increase the immune response and, with that, theoretically generate a higher response of protective antibodies.

However, repeated exposure to vaccine components such as aluminum could be harming children. As Hooker shared, “28 vaccines are given in the first year of life, one vaccine on the first day of life and upwards to eight vaccines when an infant is just 2 months old. If you look at the aluminum toxicity alone, it far surpasses the single-day toxicity limit for aluminum exposure in newborns.”12

A study funded by the U.S. Centers for Disease Control and Prevention (CDC) found that, among children with and without eczema, exposure to vaccine-associated aluminum was positively associated with persistent asthma. There was a 1.26- and 1.19-times higher risk of persistent asthma for each additional milligram of vaccine-related aluminum exposure, respectively, for children with and without eczema.13

Children who received all or most of the recommended childhood vaccines that contain aluminum received a cumulative aluminum exposure dose of more than 3 milligrams (mg). This group had, at least, a 36% higher risk of developing persistent asthma than children who received fewer vaccines, and therefore had a less than 3-mg exposure to aluminum.14

The study was observational in nature and stopped short of saying that it proves a link between aluminum-containing vaccines and asthma. The CDC also stated that it has no intention of altering its vaccine recommendations based on this study alone.15 However, the researchers pointed out that rates of asthma in U.S. children steadily increased in the 1980s and 1990s, then remained steady since 2001.

The 2001 date is significant, as most aluminum-containing vaccines were added to the childhood vaccine schedule before 2001. This includes, for example, diphtheria, tetanus, and acellular pertussis (DTaP), hepatitis B, some formulations of Haemophilus influenzae type b (Hib) and pneumococcal conjugate vaccines. According to the study:16

“There are many environmental and genetic risk factors for asthma, and any contribution from vaccine-associated aluminum has not been proven or supported through replication. However, because most aluminum-containing vaccines were added to the routine schedule prior to 2001 … observed national trends in asthma prevalence during childhood are not incongruous with the effect estimates observed here.”

COVID Shots Caused 30 Child Deaths for Every One Saved

COVID-19 shots were added to the U.S. childhood, adolescent and adult vaccine schedules after a unanimous (15-0) vote by the U.S. CDC’s Advisory Committee on Immunization Practices (ACIP). By adding the shots to the vaccine schedule, it paves the way for U.S. schools to require them for attendance.

Pfizer and Moderna, the shots’ makers, were also granted permanent legal indemnity, which otherwise would have disappeared once COVID-19 shots were no longer protected under emergency use authorization (EUA).17 Yet the shots have proven disastrous for children.

Hooker told the roundtable research shows “that for every one child that is saved from death from COVID-19, there are 30 child deaths associated with the COVID-19 vaccine. So, the risk-to-benefit ratio in terms of mortality is 30 to 1.”18

A now-retracted narrative review published in the journal Cureus called for a global moratorium on mRNA COVID-19 shots,19 citing significant increases in serious adverse events among those who received the injections, along with an “unacceptably high harm-to-reward ratio.”20

When factoring in absolute risk and the “number needed to vaccinate” (NNV), a metric used to quantify how many people need to be vaccinated to prevent one additional case of a specific disease, the review found “for every life saved, there were nearly 14 times more deaths caused by the modified mRNA injections.”21

The authors of the paper also said the shots should be immediately removed from the childhood vaccine schedule, while boosters should also be suspended. “It is unethical and unconscionable to administer an experimental vaccine to a child who has a near-zero risk of dying from COVID-19 but a well-established 2.2 percent risk of permanent heart damage based on the best prospective data available,” the paper notes.22

Heart damage from the shots includes myocarditis, which is inflammation of the heart muscle that can cause heart failure, abnormal heartbeat and sudden death. “Myocarditis is a serious disorder and 76% of all cases following COVID-19 vaccination, as reported to the Vaccine Adverse Event Reporting System [VAERS], required emergency care and/or hospitalization,” Hooker said. However, the “CDC significantly downplays myocarditis as a side effect of the vaccine.”23

Health Agency ‘Never Submitted’ Required Vaccine Safety Reports to Congress

The roundtable discussion occurred as part of a larger discussion on “Federal Health Agencies and the COVID Cartel.” The group included medical experts, political figures, journalists and whistleblowers who accused government, media and Big Pharma of censorship and coverups related to COVID-19 jab injuries.24

Hooker testified that the 1986 National Childhood Vaccine Injury Act requires the U.S. Department of Health and Human Services (HHS) to “report to Congress on the state of vaccine safety in the U.S. every two years.” However, he said HHS has “never submitted a vaccine safety report to Congress.”25

Hooker also reported that health agencies have data on health outcomes for vaccinated and unvaccinated children, but they refuse to make it public. The data, which includes close to 30 years’ worth of information on more than 10 million people, is housed in a database called Vaccine Safety Datalink.

Despite Hooker making more than 120 Freedom of Information Act (FOIA) requests, and going through “congressional representatives to get the Vaccine Safety Datalink itself,” he says, “It is simply something that they will not do.”26 He believes financial conflicts of interest are the reason why:27

“CDC buys and sells $5 billion worth of vaccines a year through the Vaccines for Children program. They also spend half a billion dollars a year … advertising and through public relationship campaigns for vaccinations in general, as compared to a woeful budget of $50 million that is being used for vaccine safety every year.”

In a discussion on Steve Bannon’s “War Room,” Hooker added that, as it stands, public health agencies are not protecting the public from vaccine injuries — something to carefully consider in your own medical decisions regarding vaccinations:28

“The CDC, FDA and NIH (National Institutes of Health) are derelict in their duty … to protect children and adults against vaccine injury in order to report to Congress the state of vaccine safety science, and their responsibility to the American public and to public health in order to protect the American public.”

[…]

Via https://articles.mercola.com/sites/articles/archive/2024/05/22/childhood-vaccine-schedule.aspx

After trying really, really hard, CDC found a 2nd case of conjunctivitis and attributes it to bird flu

https://www.cdc.gov/media/releases/2024/s0522-human-case-h5.html

Dr Meryl Nass

Case Background

A dairy worker who was being monitored because of their work exposure to H5N1-infected cattle reported symptoms to local health officials. Two specimens were collected from the patient. An upper respiratory tract specimen collected from the worker’s nose was negative for influenza virus at the state health department laboratory. The eye specimen was sent to CDC for testing because it is one of a few labs where those specimens can be used with the CDC A(H5) test. The specimen was received by CDC and testing results confirmed A(H5) virus infection. The nasal specimen was retested at CDC and confirmed to be negative for influenza. The state was then notified of the results. The designation of the influenza virus neuraminidase (the N in the subtype) is pending genetic sequencing at CDC. Attempts to sequence the virus in the clinical specimen are underway and will be made available within 1-2 days if successful. Additional genetic analysis will look for any changes to the virus that could alter the agency’s risk assessment.

Conjunctivitis (eye infection) has been associated with previous human infections with avian influenza A viruses and is part of the current CDC case definition for A(H5N1) surveillance. While it’s not known exactly how eye infections result from avian influenza exposures, it may be from contamination of the eye(s), potentially with a splash of contaminated fluid, or touching the eye(s) with something contaminated with A(H5N1) virus, such as a hand. High levels of A(H5N1) virus have been found in unpasteurized milk from H5N1-infected cows.

CDC Activities—[Be impressed. Be Very Impressed—Nass]

This case was detected through the state’s implementation of CDC’s recommended monitoring and testing strategies in exposed persons. In addition to enhanced and targeted surveillance, CDC also has:

  • Held numerous weekly engagements with state and local HDs around increasing their preparedness posture
  • Updated interim recommendations for worker protection to include those who work with dairy cows
  • Issued a Health Alert Notice (HAN) on identification of human infection and recommendations for investigations/response
  • Held a call with states asking them to move from preparedness to readiness
  • Updated interim recommendations for worker protection to include those who work in slaughterhouses
  • Conducted numerous calls with groups representing farmworkers
  • Asked states to furnish PPE for farmworkers [for conjunctivitis. Really?]
  • Announced incentives for workers who participate in public health research efforts into the outbreak. [Pay workers to get tested so CDC can claim it found more cases]
  • Asked states to work with clinical labs to increase submissions of positive influenza virus samples to public health labs for subtyping

Given the high levels of A(H5N1) virus in raw milk from infected cows, and the extent of the spread of this virus in dairy cows, similar additional human cases could be identified. Sporadic human infections with no ongoing spread will not change the CDC risk assessment for the U.S. general public, which CDC considers to be low.

CDC Recommendations

  • People should avoid close, long, or unprotected exposures to sick or dead animals, including wild birds, poultry, other domesticated birds, and other wild or domesticated animals (including cows). [In other words, let your pets and livestock die rather than handfeeding them, etc.?]
  • People should also avoid unprotected exposures to animal poop, bedding (litter), unpasteurized (“raw”) milk, or materials that have been touched by, or close to, birds or other animals with suspected or confirmed A(H5N1) virus. [PPE to change the chicken bedding?]
  • CDC has interim recommendations for prevention, monitoring, and public health investigations of A(H5N1) virus infections in people. CDC also has updated recommendations for worker protection and use of personal protective equipment (PPE).
  • Following these recommendations is central to reducing a person’s risk and containing the overall public health risk. [Which is near zero now.]

More information is available on the CDC website at https://www.cdc.gov/flu/avianflu/avian-flu-summary.htm.

[1] first human case of A(H5N1) bird flu in the United States linked to an outbreak in dairy cows was also the first likely case of human infection with A(H5N1) from a cow globally. [In other words, no other countries have agreed to perform the same charade as CDC is doing with cows.] This was reported on April 1, 2024. The person reported eye redness as their only symptom, consistent with conjunctivitis, and recovered. Learn more about this case in a letter published in the New England Journal of Medicine titled Highly Pathogenic Avian Influenza A(H5N1) Virus Infection in a Dairy Farm Worker. The April 1 case was actually the second human case of A(H5N1) reported in the United States. The first human case of A(H5N1) bird flu in the United States was reported in 2022 in a person in Colorado who had direct exposure to poultry and who was involved in depopulating poultry with presumptive A(H5N1) bird flu. The 2022 human case was not related to dairy cattle. The person only reported fatigue without any other symptoms and recovered. Learn more at U.S. Case of Human Avian Influenza A(H5) Virus Reported.

[…]

Via https://merylnass.substack.com/p/major-cdc-press-release-after-trying

Peter Daszak Gets DOD and CIA Funding. Why Don’t They Ask About That?

Who is Peter Daszak, exec who sent taxpayer money to Wuhan lab?

Peter Daszak is the President of EcoHealth Alliance, the organization most closely associated with the potential lab leak at the Wuhan Institute of Virology (WIV) that may have started the Covid crisis.

The U.S. House Committee on Oversight and Accountability has recently done a lot of “research” on Daszak and EcoHealth, resulting in a published report on May 1, 2024 with the earth-shattering finding that there exist “serious and systemic weaknesses in the federal government’s—particularly NIH’s—grant making processes.” Furthermore, these very bad weaknesses “not only place United States taxpayer dollars at risk of waste, fraud, and abuse but also risk the national security of the United States.”

This sounds pretty serious: Our taxpayer dollars and our national security are at risk. Some very bad things are happening, apparently. What are those bad things? “Weaknesses in the NIH’s grant making process.” Is that really all the Committee could come up with? If those grant-making weaknesses are so terrible, what does it recommend we do about them?

Based on its findings, the Committee recommended some very broad, but not very specific, actions:

  1. To Congress: “Reign in [they used “reign” instead of “rein” – a noteworthy Freudian slip] the unelected bureaucracy, especially within government funded public health.
  1. To the Administration: Recognize EcoHealth and its President, Dr. Daszak, as bad actors…and ensure neither EcoHealth nor Dr. Daszak are awarded another cent, especially for dangerous and poorly monitored research.

The Administration must have taken heed, because a mere two weeks later, on May 15, 2024, the Subcommittee made this triumphant announcement:

“HHS has begun efforts to cut off all U.S. funding to this corrupt organization. EcoHealth facilitated gain-of-function research in Wuhan, China without proper oversight, willingly violated multiple requirements of its multimillion-dollar National Institutes of Health grant, and apparently made false statements to the NIH. These actions are wholly abhorrent, indefensible, and must be addressed with swift action.”

Note the bizarre disconnect between the description of “this corrupt organization” and its “abhorrent, indefensible” actions, and the accusations leading to such extreme claims, which include conducting research without proper oversight (nobody ever does that!), violating requirements of its NIH grant (a bureaucratic infraction) and “apparently” making false statements to the NIH (not even for sure).

In any event, “swift action” must be taken. What exactly is that action?

“HHS has begun efforts to cut off all U.S. funding” to EcoHealth. “Begun efforts” – sounds like concrete results are imminent. Not just imminent but consequential. Like “future debarment” and “funding suspension.” (sarcasm intended)

But wait. Didn’t they already do that? Yes, they did.

2020 funding suspension

Quick reminder: On April 24, 2020, the NIH canceled funding for Wuhan Institute of Virology (WIV) gain-of-function research led by EcoHealth Alliance, because the Trump Administration suspected (or knew) such research may have had something to do with the Covid pandemic.

The scientific world was outraged. Seventy-seven U.S. Nobel Laureates and 31 scientific societies wrote to NIH leadership requesting review of the decision. Gain-of-function research must continue! In August 2020 the NIH reversed the cancellation and started funding EcoHealth and WIV again. [ref]

The Nobel Laureates and scientific societies won the day: Humanity-saving research to develop deadly pathogens not found in nature could continue unhindered by radical NIH funding cuts.

And yet: NIH grants are a mere fraction of EcoHealth Alliance’s overall government funding.

So which funds are being “suspended” this time around?

Actually, none.

The very threatening “notice of suspension and proposed debarment” sent to EcoHealth Alliance by HHS on May 15, 2024, reassures the organization (whose behavior has been abhorrent and indefensible) that “suspension and debarment actions are not punitive.”

We’re not trying to punish you for your bad behavior, the letter says. We just want to make sure there are non-punitive “consequences” for that behavior. For example:

Offers will not be solicited from, contracts will not be awarded to, existing contracts will not be renewed or otherwise extended for, and subcontracts requiring United States Federal Government approval will not be approved for EHA [EcoHealth Alliance] by any agency in the executive branch of the United States Federal Government, unless the head of the agency taking the contracting action determines that there is a compelling reason for such action.

[BOLDFACE ADDED]

In other words, if the head of the “agency taking the contracting action” determines there is “a compelling reason” to contract with Ecohealth, then this whole suspension and debarment thing is moot. So not punitive. And, pretty much, no consequences. And, also, no funds “suspended.”

Nevertheless, given the horrendous behavior of EcoHealth, as detailed in the announcement of the non-punitive consequences – how could any government agencies possibly have compelling reasons to engage in “contracting action” with “this corrupt organization”?

EcoHealth is mostly funded by the State Department and Pentagon

In an extensive expose on Peter Daszak and EcoHealth Alliance, The Intercept reported in December 2021:

EcoHealth Alliance’s funding from the U.S. government, which Daszak has said makes up some 80 percent of its budget, has also grown in recent years. Since 2002, according to an Intercept analysis of public records, the organization has received more than $118 million in grants and contracts from federal agencies, $42 million of which comes from the Department of Defense. Much of that money has been awarded through programs focused not on health or ecology, however, but on the prevention of biowarfare, bioterrorism, and other misuses of pathogens.

[BOLDFACE ADDED]

Here’s what nearly two decades of government funding for EcoHealth Alliance looks like (graph from Intercept article):

As RFK Jr. wrote, based on this information, in The Wuhan Cover-Up:

By far, Daszak’s largest funding pool was the CIA surrogate, the United States Agency for International Development (USAID). Through USAID, the CIA funneled nearly $65 million in PREDICT funding to EcoHealth between 2009 and 2020.

(p. 228, Kindle Edition)

Yet another article examining Daszak’s military/biodefense ties appeared in Independent Scientist News in December 2020, reporting that most of EcoHealth Alliance’s Pentagon funding “was from the Defense Threat Reduction Agency (DTRA), which is a branch of the DOD which states it is tasked to “counter and deter weapons of mass destruction and improvised threat networks.”

Furthermore,

The military links of the EcoHealth Alliance are not limited to money and mindset. One noteworthy ‘policy advisor’ to the EcoHealth Alliance is David Franz. Franz is former commander of Fort Detrick, which is the principal U.S. government biowarfare/biodefense facility.

The ISN article also provides a handy spreadsheet detailing EcoHealth funding.

So what is the Oversight Committee overlooking – and why?

There is no mention of DoD, DTRA or USAID funding in the Committee’s announcement or in the utterly performative, 100% toothless notice of suspension and debarment they sent to Peter Daszak. Does the U.S. House Committee on Oversight and Accountability not know who the major government funders of EcoHealth Alliance are?

If any agency can bypass the suspension and debarment by “determining that there is compelling reason” to fund EcoHealth, what is the point of those non-punitive consequences?

Why this charade of accountability when, in fact, the supposed overseers are willfully ignoring what’s actually going on?

Clearly, the Committee is not interested in investigating Daszak’s role in the biodefense industry that was responsible not just for the gain-of-function research that may have created SARS-CoV-2, but for the entire Covid pandemic response – which was most definitely not about public health and was, in fact, all about creating and administering the medical countermeasures which were the monomaniacal focus of the biodefense responders.

What to ask Peter Daszak if we had actual oversight

If the Committee were serious about investigating Peter Daszak and EcoHealth Alliance, here are some questions they would ask:

Non-public health funding sources and projects

  • Most of the government funding for EcoHealth Alliance comes not from public health agencies but from USAID (State Department/CIA) and the Pentagon. What projects are these non-public health agencies funding? Are these projects related to biodefense/biowarfare research?
  • Is the USAID and Pentagon-funded virus research conducted by EcoHealth and/or its partners intended primarily to prepare for naturally occurring pandemics or for potential biowarfare/bioterrorism attacks?
  • Do the USAID and Pentagon-funded projects conducted by EcoHealth and/or its partners involve creating pandemic potential pathogens as part of biodefense/biowarfare research?
  • Do you know or suspect that SARS-CoV-2 was an engineered virus created as part of a USAID and Pentagon-funded biowarfare/biodefense project?
  • Do the USAID and Pentagon-funded projects conducted by EcoHealth and/or its partners involve work on medical countermeasures against potential biowarfare/bioterrorism agents?

Disease X op-ed

  • On February 27, 2020, before the Covid pandemic had been declared and before anyone in the U.S. had died of Covid-19, you wrote an op-ed for The New York Times stating that the novel coronavirus was “Disease X.” You explained that the term Disease X was coined by you and a bunch of experts at the World Health Organization in 2018. In your report from 2018, it says:

“Disease X represents the awareness that a serious international epidemic could be caused by a pathogen currently not recognized to cause human disease. Disease X may also be a known pathogen that has changed its epidemiological characteristics, for example by increasing its transmissibility or severity.”

Why were you so sure, so early on, even before we knew there was a pandemic, that this was Disease X? What was it about SARS-CoV-2 (which, after all, was named as a direct successor of the original SARS, to which it was said to be very similar) that made it seem so uniquely dangerous to you? Why did you feel you had to warn the whole world about it on the pages of the NYT? 

  • Did you think SARS-CoV-2 was a known pathogen that had “changed its epidemiological characteristics” by “increasing its transmissibility or severity”? If yes, what made you think that?
  • Did you think SARS-CoV-2 was a potential bioweapon that had been developed using funds from USAID and DOD by EcoHealth Alliance and/or its research partners in China or elsewhere?
  • The New York Times has subsequently erased your Disease X op-ed from their online 2/27/2020 issue. You can only find it through the direct link. Why do you think they have made it all but impossible for anyone who doesn’t already know about the article to find it? Do you regret having written it?

Linking Disease X to genetic vaccine platforms

  • In the NYT op-ed, you provided a link from the term “Disease X” to a 2018 CNN article in which Dr. Anthony Fauci says that, in order to combat such dangerous as-yet-nonexistent pathogens, “the WHO recognizes that it must “nimbly move” and that this involves creating “platform technologies.”

Fauci goes on to say that “scientists develop customizable recipes for creating vaccines. Then, when an outbreak happens, they can sequence the unique genetics of the virus causing the disease, and plug the correct sequence into the already-developed platform to create a new vaccine.”

That sounds an awful lot like the mRNA platform used for the Covid countermeasures that came to be known as the “mRNA vaccines.”

Why did you link to that particular article from your op-ed about disease X? Were you suggesting that the solution to the pandemic that you appeared to be predicting would be a genetic platform in which the “correct sequence” could be plugged to create vaccines?

  • Were you already aware of the Covid mRNA vaccines being developed at the time of your op-ed (February 27, 2020) by Moderna and BioNTech/Pfizer, long before the official launch of Operation Warp Speed (May 2020)?
  • Is it true that the Pentagon considered the mRNA platforms to be the preferred countermeasures against Covid-19, and that these were always intended to reach full funding and development, starting all the way back in January 2020?
  • Was the USAID and Pentagon-funded research conducted EcoHealth and/or its partners related to the development of such mRNA vaccines? If so, how?

[…]

Via https://debbielerman.substack.com/p/peter-daszak-does-biodefense-work

 

US-Europe Divisions Deepen Over Palestinian Statehood

A man waving a Palestinian flag, 2024.A man waving a Palestinian flag, 2024. | Photo: X/ @szetotm

teleSUR Newsletter

The U.S. continues to oppose the growing wave of countries joining the recognition of the Palestinian state.

On Wednesday, Norway, Ireland and Spain decided to recognize Palestine as a state, marking a significant shift in European policy more than seven months into the current Israeli offensive against Gaza.

However, U.S. National Security Advisor Jake Sullivan dismissed the three nations’ move as “unilateral recognition”, asserting that President Joe Biden believes the two-state solution should be achieved “through direct negotiations through the parties.”

As Israel and Hamas failed to reach a ceasefire agreement during talks in Cairo earlier this month mediated by Egypt, Qatar, and the United States, the U.S. opposition to the recognition has highlighted expanding transatlantic divisions.

RECOGNITION WAVE

In Wednesday’s coordinated announcements, Norway was the first to act. Norwegian Prime Minister Jonas Gahr Store declared at a press conference that “a Palestinian state is a prerequisite for achieving peace in the Middle East.”

Ireland quickly followed. In Dublin, Irish Prime Minister Simon Harris said the decision should not have to wait “indefinitely” when it is “the right thing to do.” He expressed confidence that more countries would take this important step in the coming weeks.

Spain joined in soon after. Spanish Prime Minister Pedro Sanchez said that Spain recognizes Palestine “for peace, for justice, and for consistency,” urging both parties to engage in dialogue to achieve a two-state solution.

The text reads, “Historic!! ‘Today, Ireland, Norway, and Spain announce that we recognize the State of Palestine,’ said the Irish Prime Minister. The Europe of honor is leading the way. Other countries will follow. There will be no turning back.”

In the past week, several other European countries, including Malta and Slovenia, have also signaled their intent to follow suit. Belgian Prime Minister Alexander De Croo said Wednesday that Belgium was waiting for the “right moment.”

Shada Islam, a Brussels-based commentator on EU affairs, suggested that the recognition by Norway, Ireland, and Spain is “almost certainly” going to be followed by Belgium, Malta, and Slovenia in the coming weeks.

Some of the United States’ traditional allies are considering recognition. French Foreign Minister Stephane Sejourne said that such recognition is not taboo, though he stressed the timing, saying conditions had not yet been met. German Foreign Minister Annalena Baerbock made a similar statement.

Wednesday’s recognition drew anger from Israel, which announced it is recalling its envoys to the three countries.

EXPANDING U.S.-EUROPE RIFTS

While the recognition has received mixed reactions in Europe, the continent’s stance on Israel has gradually shifted, especially as more than 35,000 Palestinians have been killed since Oct. 7, 2023. This shift has exposed rising rifts between the United States and Europe.

Store also revealed that Norway supports granting Palestine full membership status in the United Nations. The U.S., however, vetoed a draft resolution in April recommending that the General Assembly admit Palestine to the United Nations, drawing widespread disappointment.

Britain and Switzerland abstained from the vote, while the remaining members of the United Nations Security Council (UNSC) voted in favor.

Days earlier, the United States showed support for Israel by denouncing an International Criminal Court (ICC) application to arrest two Israeli government officials, including Prime Minister Benjamin Netanyahu, and three Hamas leaders.

Biden called the application “outrageous,” saying that “we will always stand with Israel against threats to its security.” In April, Biden also piled up U.S. aid to Israel by signing a security assistance bill that included approximately US$14.1 billion in funding to support Israel.

The Biden administration is considering potential sanctions against the ICC over the arrest request, said U.S. Secretary of State Antony Blinken on Tuesday. The United States and Israel are not members of the ICC.

In contrast, the French Foreign Ministry stated its support for the ICC, saying it supports “the fight against impunity in every situation.” Belgian Minister of Foreign Affairs Hadja Lahbib called the ICC request “an important step in the investigation of the situation in Palestine.”

EU foreign policy chief Josep Borrell asserted that “all states that have ratified the ICC statutes are bound to execute the Court’s decision.”

As United Nations agencies continued to warn of dire consequences in Gaza, including famine and epidemics, EU leaders in March unanimously called for “an immediate humanitarian pause leading to a sustainable ceasefire” in Gaza.

[…]

Via https://www.telesurenglish.net/news/US-Europe-Divisions-Deepen-Over-Palestinian-Statehood-Issue-20240523-0003.html

The Vaccine Mafia is Getting Nervous

They have a lot of money to lose if the WHO treaties don’t go through. So their manure and their lies just don’t stop. I love their desperation.

Look who the first 8 authors are of this hit piece, claiming we are the disinformationists! Sarah Gilbert was a coinventor of the Astra-Zeneca COVID vaccine that killed thousands of young women with brain clots, including a BBC radio presenter. Instead of crawling into a hole and hiding herself, she is begging to be allowed to invent yet more disastrous vaccines for the world.

Prof Petro Terblanche is managing director of Afrigen Biologics, South Africa, which hosts the WHO’s global mRNA technology vaccine hub.

Dr Jerome Kim is Director General of the International Vaccine Institute, South Korea.

Rajinder Suri is CEO of Developing Countries Vaccine Manufacturers Network, India.

Prof Padmashree Gehl Sampath is CEO of the Africa Pharmaceutical Technology Foundation, Rwanda.

Prof Kiat Ruxrungtham is founder and co-director of the Vaccine Research Center  at Chulalongkorn University, Thailand. 

Frederik Kristensen is managing director of the Regionalized Vaccine Manufacturing Collaborative and Coalition for Epidemic Preparedness Innovation.

Ramon Rao is CEO of Hilleman Laboratories, Singapore, which translates early discovery of vaccines and biologics for infectious diseases into affordable products with global health impact.

Prof Sarah Gilbert is Saïd Professorship of Vaccinology at Oxford University UK, and co-developed the Oxford-AstraZeneca COVID-19 vaccine.

The Pandemic Agreement: A Bridge to Nowhere or North Star to Access and Global Health Security?

https://healthpolicy-watch.news/the-pandemic-agreement-a-bridge-to-nowhere-or-north-star-to-access-and-global-health-security/

Sixteen leading scientists and manufacturers involved in vaccine development and production worldwide issue an urgent call for a pandemic accord that can be a ‘win-win for all.’ The full list of authors is available below.

Health misinformation was not invented during COVID-19 but was certainly brought to a higher, more malevolent  and destructive pitch during the pandemic.  That hostile crusade has since been (mis)directed at two landmark agreements, the Pandemic Prevention, Preparedness and Response Agreement (Pandemic Agreement), and amendments to the International Health Regulations (IHR), that are currently being negotiated by WHO’s 194 member states for approval at the World Health Assembly.

The overarching goal of ensuring that the world will deal more equitably with the next pandemic appears to be elusive as we near the deadline of May 2024 for the close of the negotiations.

Several social media and news outlets have claimed that the WHO is negotiating two instruments that will afford the agency far-reaching powers in case of a future pandemic….

[…]

Via https://merylnass.substack.com/p/the-vaccine-mafia-is-getting-nervous

The Media Slowly Backpedals, As They Slowly Erase the False Narrative

Mark Oshinskie

[…]

Media outlets and writers who fomented Coronamania have, over the past two years or so, been retreating slowly from the fear and loathing they began brewing up in March, 2020. They’ve calculated that a Covid-weary, distractable public won’t remember most of what they said earlier in the Scamdemic.

Last Friday, in two, paired articles, New York Times writers Apoorva Mandavilli and David Leonhardt continue this strategically slow retreat from the Covid lies they’ve sponsored. For the first time, they acknowledge that maybe the shots they’ve praised have caused a few of what jab-o-philic readers will dismiss as minor injuries.

As he begins his summary of Mandavilli’s theme, Leonhardt admits that the notion that vaxx injuries occurred makes him “uncomfortable.” He’s not expressing discomfort about the injuries themselves. He’s concerned that the vaxx critics might be proven correct.

Why would a self-described “independent journalist” be made uncomfortable by facts? What’s so repugnant about simply calling balls and strikes? Why does Leonhardt have a rooting interest? What’s so hard about admitting he’s been wrong, not just about the shots, but about all of the Covid anxiety he and his employer have incited throughout the past three-plus years?

Bear this in mind: In early 2021, Leonhardt went on a 1,600-mile road trip to get injected as early as he could. David, kinda neurotic and def not climate friendly.

Admitting error—or outright complicity with the Scam—during the Covid overreaction would entail losses of face and credibility. After all the harm the media has done, those consequences would be just and proper.

To avoid this result, the media and bureaucrats are backpedaling slowly to try to change their views without too many people noticing. In so doing, they’re very belatedly adopting the views of those, like me, who from Day 1, called out the hysteria driving, and the downsides to, the Covid overreaction.

But while they’ve incrementally changed parts of their message, they hold tightly to the central, false narrative that Covid was a terrible disease that indiscriminately killed millions. The Covophobes continue to falsely credit the Covid injections for “saving millions of lives” and “preventing untold misery.”

Times readers are a skewed, pro-jab sample. Thus, about half of the 1000+ commenters adopt Mandavilli’s and Leonhardt’s mythology that, even if the shots injured people, they were a net positive in a world facing a universally vicious killer. Relying on that false premise, these columnists and the commenters assert that no medical intervention is risk-free and that a few metaphorical eggs were inevitably broken while making the mass vaccination omelet. In their view, such injuries are a cost of doing business.

To begin with, where was such risk/reward analysis when the lockdowns and school closures were being put in place?

Moreover, The Times writers and most pro-jab commenters pretentiously and inappropriately claim the mantle of “Science.” To many, modern medicine is a religion and “vaccines” are a sacrament. Their pro-vaxx faith is unshakable. But these ostensible Science devotees unreasonably overlooked Covid’s clearest empirical trend: SARS-CoV-2 did not threaten healthy, non-old people. Therefore, neither non-pharmaceutical interventions (“NPIs”) nor shots should have been imposed upon those not at risk. The NPI and shot backers weren’t Scientists. They were Pseudo-Scientists.

The Times’s stubborn, apocalyptic Covid narrative and pro-vaxx message has never squared with what I’ve seen with my own eyes. After four years in Covid Ground Zero, high-density New Jersey, and despite having a large social sphere, I still directly know no one who has died from this virus. I indirectly know of only five—relatives of acquaintances—said to have been killed by it. Each ostensible viral victim fits the profile that’s been clear since February, 2020: very old and unhealthy, dying with, not from, symptoms common to all respiratory virus infections, following a very unreliable diagnostic test.

Countering the intransigent shot backers, hundreds of commenters to the Mandavilli piece describe non-lethal injuries they sustained shortly after injecting. But both articles, and many commenters to the Mandavilli article, emphasize that “correlation isn’t causation.”

The persuasiveness of correlation is typically questioned only when one would viscerally prefer not to apply Occam’s Razor and adopt the most straightforward explanation for symptoms that began shortly after injection. I suspect that, in their personal dealings, those who say “correlation isn’t causation” seldom believe in coincidences.

I directly know six people who’ve had significant health setbacks shortly after taking the shots, including one death. These seem like too many coincidences. Further, what would provide convincing proof of vaxx injury causation? Autopsies are, perhaps strategically, rare. Having done litigation, I know experts will always disagree about causation if they’re paid well enough. And ultimately, doesn’t the cited “millions saved” study assume that correlation is causation?

While the peremptory assertions that the shots saved millions of lives are very questionable and poorly supported, many who read these statements will cite these as gospel because “millions” is a memorable, albeit speculative and squishy figure, and because, well, The New York Times said so!

While the columnists use this phony stat to justify mass vaccination, only one in five-thousand of those infected—nearly all of them very old and/or very sick or killed iatrogenically—had died “of Covid” before VaxxFest began. The vast majority of these deceased were likely to die soon, virus or no.

Thus, how can one say that the shots saved millions of lives? For how long were they saved? And did those who conducted the cited “millions of deaths” study believe they’d get future—professional lifeblood—grants if they didn’t find that the shots saved millions of lives?

Further, Mandavilli and Leonhardt never acknowledge—and may not even know of— the statistical sleight of hand that’s been used throughout by the jab pushers. I’ve described these tricks in prior posts. For example, there was “healthy vaccinee bias:” those who administered the shots strategically declined to inject those who were so frail that the shots’ systemic shock might kill them. And those who injected weren’t counted as “vaxxed” until 42 days after their first shot. As the shots initially suppress immunity and disrupt bodies, one should expect the shots to increase deaths in the weeks after the shot regimen begins. Injectees who died within this initial 42 days were falsely categorized as “unvaxxed.”

FWIW, my wife and I and all other non-vaxxers I know have predictably been fine. The shots didn’t save any of our lives or keep us out of the hospital. Our immune systems did. “The Virus’s” lethality was badly overhyped.

More medical intervention doesn’t necessarily improve health. To the contrary, and especially regarding the shots, less is often more.

While Mandavilli and others blame “vitriolic” anti-vaxxers for discouraging vaxx and booster uptake, vaxx failure itself more strongly discouraged injections than did anything any anti-vaxxer said. The government and media repeatedly touted the shots as “safe and effective” and guaranteed that they would “stop infection and spread.” Montages of these clips are likely still on the Net. Yet, countless injectees—including all injectees whom I know—have gotten sick, several times each.

Consequently, jabbers felt lied to. Based on such directly observable data of vaxx failure and experiencing or seeing vaxx injuries, and without reading studies or conducting courtroom trials, the public made its own observations and rendered its negative verdict about vaxx efficacy and safety by declining vaxx “boosters.” Besides, if anti-vaxxers held such sway over public opinion that they could stop people from taking boosters, their initial warnings would have stopped people from taking the initial shots.

Importantly, and by extension, as we skeptics were right about the shots, we were also right when we criticized the lockdowns, school closures, masks and tests that have been articles of Coronamanic faith. A recent CDC study so has so concluded.

Many of NPI and shot backers have taken refuge in “We-Couldn’t-Have-Known-ism.” But millions, including me, did know, based on widely available information, that the NPIs and shots were always bad ideas. And as we knew that only the old and ill were at risk and that the NPIs would cause great harm, those who are very belatedly admitting that “mistakes were made” not only also could have known; they should have known. Their failure to know reveals either a willful, opportunistic, tribalistic disregard of plainly observable information or a lack of intelligence.

Throughout the Scamdemic, Mandavilli and Leonhardt have belatedly, incrementally changed their disproven views. Their untenable alternative was to persist with a plainly failed narrative and trade in their credibility chips, issue-by-issue. But they’re doing so slowly to evade responsibility for being wrong when it mattered.

For example, for two years, Mandavilli strongly supported keeping schoolkids home. Similarly, 41 months after the Scamdemic began, Leonhardt quoted, with apparent surprise, an “expert” who says that Covid deaths correlate closely with old age. By the time they made these concessions, most of the public already knew that the columnists’ notions were wrong to begin with.

It also took Leonhardt 41 months to admit that Covid deaths were significantly overcounted. But, as when drivers who exhale a .25% blood alcohol level say they “only had a couple of beers,” neither Leonhardt nor the rest of the Covid-crazed will admit how much these numbers were strategically inflated.

Leonhardt had also backed Paxlovid, which has long since been widely devalued.

And Leonhardt very belatedly admitted that infection confers immunity: first to individuals, then to the group. By so conceding, he was merely validating a basic epidemiological principle—herd immunity—that was widely accepted before March, 2020 but, from 2020-22, was used to vilify those who stated it.

Further, while Leonhardt and Mandavilli continue to sell the phony “Pandemic of the Unvaccinated” narrative, far more vaxxed, than unvaxxed people have died with Covid.

Conspicuously, Mandavilli and Leonhardt also fail to mention that hundreds of thousands have suffered apparent vaxx injuries or deaths from heart attacks, strokes or cancers and that overall deaths have increased in highly vaxxed nations. Thus, when one considers all causes of death, the shots seem to have caused a net loss, not gain, in life span.

The Times writers ignore the tens of thousands of American post-vaxx deaths listed in the user-unfriendly, and therefore underused, VAERS database and the excess death increases in the most highly vaxxed nations in 2021-22. Unlike the vaxx injured, who are still alive, dead vaccinees tell no tales. Nor do most of their survivors because, as with families who’ve lost a young man in a war, those left to mourn don’t want to believe that their beloved has died avoidably or in vain. The reluctance to attribute deaths to the shots is particularly acute if the bereaved encouraged the decedent to inject.

While Mandavilli and Leonhardt now begrudgingly report that the shots may not, despite all of the ads and bureaucratic assurances, have been so safe after all, conceding that the shots have killed people is a bridge too far. At least for now.

But the Overton Window has been opened. Thus, the media backpedaling will continue, albeit slowly. Vaxx injuries and NPI-induced damage are not emerging trends. They’re established trends that deserve much more coverage than they’ve received. The lockdown/mask/test/vaxx supporters have been thoroughly wrong throughout. They have no credibility chips left.

I derive little satisfaction from watching their pro-vaxx/NPI case crumble. Firstly, unlike in a courtroom, where judges and juries are, at least in theory, focused on what witnesses say, most peoples’ attention is too scattered to notice the Covid fearmongers’ reversals. The media’s retreat has occurred very slowly. As the backtracking fearmongers have cynically calculated, the public’s Covid fatigue will blunt anti-media anger.

[…]

Via https://markoshinskie8de.substack.com/p/erasing-coronamania

 

U.S. Bankrolling Creation of Deadlier, More Contagious Bird Flu Strains

chicken and glove holding vial with words "bird flu: positive"

Under the guise of creating bird flu vaccines, U.S. government agencies and private funders like the Bill & Melinda Gates Foundation are bankrolling gain-of-function research to make bird flu viruses more lethal and transmissible among mammals.

U.S. health officials only recently admitted to funding gain-of-function research at the Wuhan Institute of Virology in China — but for decades, the U.S. government has funded the same type of dangerous research on bird flu in the U.S.

And that research continues today.

The Centers for Disease Control and Prevention (CDC), the Biomedical Advanced Research and Development Authority (BARDA), the National Institute of Allergy and Infectious Diseases (NIAID), the U.S. Department of Agriculture (USDA) — even the Bill & Melinda Gates Foundation — have funded or are funding research to make bird flu more pathogenic and/or more transmissible in mammals.

Appearing on the “Kim Iversen Show” on May 16, Brian Hooker, Ph.D., Children’s Health Defense chief scientific officer, said he is concerned the U.S. is “making agents of … biological destruction” that could “put us into another pandemic.”

Hooker echoed warnings by former CDC Director Robert Redfield, who suggested the next pandemic would be sparked by a leak from a lab working to humanize bird flu viruses.

Hooker told Iversen the CDC’s Influenza Division infected ferrets with the currently circulating H5N1 avian influenza strain, then infected human lung cells, to make the virus more infective to humans.

Their justification, he said, is to be prepared for a zoonotic outbreak — where a virus from a bird or other animal jumps to humans.

“The party line that you hear all the time is, ‘Well, we have to develop these pathogens because then we can develop the countermeasures,’ — the vaccines, the monoclonal antibodies, the therapeutics,” he said.

Long list of gain-of-function studies on bird flu

The CDC, BARDA, NIAID and the World Health Organization (WHO) have conducted or funded dangerous bird flu studies.

Jessica Belser, a lead researcher with the CDC, was involved in numerous studies exploring the pathogenicity and transmissibility of bird flu viruses. She is co-author of a March 2024 study on the H5N1 strain causing fatal disease and transmitting between co-housed ferrets.

In 2020, Belser studied how different strains of the H9N2 flu virus, which have genetic and antigenic differences, show varying patterns of replication and transmission in mammalian animal models. The Chinese Center for Disease Control and Prevention was a collaborator.

In 2016, Belser studied how different bird flu strains, including H5N1, H7N9 and H9N2, could infect human pulmonary endothelial cells.

Richard Webby, Ph.D., a BARDA-associated researcher and director of the WHO Collaborating Centre for Studies on the Ecology of Influenza in Animals and Birds, is co-author of a May 2024 paper studying the susceptibility and transmissibility in the pig population of highly pathogenic avian influenza derived from mink.

In a 2017 study funded by the NIAID, Webby tested bird flu vaccines on ferrets, infecting them with the wild virus to determine the vaccines’ efficacy.

Hooker told The Defender this research is dangerous because ferrets “are immunologically very close to humans. … It’s not a huge leap for them to suddenly get into the human population and start human-to-human transmission.”

Christine Oshansky, chief of Pandemic Vaccines and Adjuvants at BARDA, co-authored a 2021 study of highly pathogenic influenza H7N9 and a vaccine formulation.

In 2018, Oshansky tested H5N1 vaccines stored in the national Influenza vaccine stockpile for up to 12 years to determine if they could be effective against divergent A (H5) influenza viruses.

The WHO funded the May 2020 study, “Pandemic potential of highly pathogenic avian influenza clade 2.3.4.4 A(H5) viruses.” Collaborators included the CDC, the Food and Agriculture Organization of the United Nations, the Chinese Center for Disease Control and Prevention, the European Centre for Disease Prevention and Control and other organizations. Webby and Yoshihiro Kawaoka, DVM, Ph.D. of the University of Wisconson are among the listed authors.

“That’s the huge danger of doing this work,” Hooker said. “Whether it’s an accidental or intentional release, you’re playing with these pathogens so that they’re basically creating variants that are infectious in humans.”

This article was funded by critical thinkers like you.

The Defender is 100% reader-supported. No corporate sponsors. No paywalls. Our writers and editors rely on you to fund stories like this that mainstream media won’t write.

The vaccine cash cow

Hooker told Iversen there are “myriad patents associated with bird flu vaccines [and] bird flu pathogens.”

Kawaoka, the researcher long funded by NIAID to conduct bird flu research, has 78 patents in his portfolio, many of them related to bird flu vaccination.

In 2023, Kawaoka filed patents on:

  • Mutations that confer genetic stability to additional genes in influenza viruses (US-11802273-B2).
  • Recombinant influenza viruses with stabilized HA for replication in eggs (US-11807872 – B2).
  • A humanized cell line (US-11851648-B2).

In 2022, Kawaoka filed a patent for influenza virus replication for vaccine development (US-113906-B2).

Richard Bright, former BARDA director and a bird flu researcher at the CDC from 1998-2006, has an “extensive patent portfolio on — you guessed it — bird flu vaccines,” Hooker said. “And so these prophets of doom hit the airwaves and they scare everybody.”

[…]

Viahttps://childrenshealthdefense.org/defender/united-states-bankrolling-creation-deadlier-contagious-bird-flu-strains/

Two Toxic Weedkillers Linked to Serious Illness Found in ALL Pregnant Women

pregnant belly and pesticides being sprayed on corn field

 

In a first-of-its-kind series of biomonitoring studies published in Agrochemicals, researchers identified the presence of the herbicides dicamba and 2,4-D in ALL pregnant participants from both cohorts in 2010-2012 and 2020-2022.

The findings from this research are not surprising given the explosion of toxic petrochemical pesticides in the Midwest region of the U.S.

“The overall level of dicamba use (kilograms applied in one hundred thousands) in the U.S. has increased for soybeans since 2015 and slightly increased for cotton and corn,” the authors reported, based on U.S. Department of Agriculture National Agriculture Statistics Service survey results.

The authors also reported:

“The overall level of 2,4-D use (kilograms applied in one hundred thousands) in the U.S. was highest in 2010 for wheat, soybeans, and corn. The amount of 2,4-D applied increased the most for soybeans and corn from 2010 to 2020.”

The researchers focused on the states of Illinois, Indiana and Ohio, given the increase in dicamba and 2,4-D during the study period for both cohorts (2010-2022).

The researchers are based at Indiana University School of Medicine in the Department of Biostatistics and Health Data Science and Department of Obstetrics and Gynecology, Quebec Toxicology Center within the Institut national de santé publique du Québec and Benbrook Consulting Services.

Charles Benbrook, Ph.D., one of the authors, served as an expert witness in herbicide litigation but stepped down as executive director of the Heartland Health Research Alliance to avoid any conflicts of interest pertaining to the studies cited in the report. The study was published online on Feb. 20.

The methodology included the analysis of urine samples from the 2010-2012 Nulliparous Pregnancy Outcomes Study that enrolled 10,0037 pregnant participants from eight study sites across the three states, as well as a “smaller nested case-control study” in which 61 samples were gathered from women enrolled in the original study, in the first trimester in 2020-2022 periods and based specifically in Indiana.

“Cases were selected as participants in which any of the following occurred: hypertensive disorders of pregnancy, spontaneous preterm birth, gestational diabetes, stillbirth, or fetal demise < 20 weeks,” according to the researchers.

The study identified metabolites found within the samples evaluated, “including herbicides (dicamba, 2,4-D, and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T)), organophosphates insecticides (malathion dicarboxylic acid (MDA), para-nitrophenol (PNP), 3,5,6-trichloro-2-pyridinol (TCPy), 2-diethylamino-6-methylpyrimidin-4-ol (DEAMPY), and 2-isopropyl-6-methyl-4-pyrimidinol (IMPY)), and synthetic pyrethroids insecticides (cis-3-(2,2-Dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acid (cis-DCCA), trans-3-(2,2-Dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acid (trans-DCCA), 3-Phenoxybenzoic acid (3-PBA), 4-Fluoro-3-phenoxybenzoic acid (4-F-3-PBA), and cis-3-(2,2-Dibromovinyl)-2,2-dimethylcyclopropane carboxylic acid (cis-DBCA)).”

“We found that dicamba in pregnant study participants increased significantly in the more recent Midwest cohort from 2020 to 2022 relative to the earlier cohort from 2010 to 2012,” the researchers arrived at this conclusion based on existing and recent studies.

“Concentration levels of 2,4-D also increased in the more recent cohort, but the difference was not statistically significant.”

There are a plethora of studies that demonstrate the adverse health effects of both dicamba and 2,4-D, even at low levels. The research reported in Agrochemicals adds to the knowledge of widespread exposure and adverse effects.

For example, a 2021 study published in Toxicology found individuals working or residing in areas with frequent pesticide use, including 2,4-D, experience more incidences of neurodegenerative disease amyotrophic lateral sclerosis, or ALS, relative to the general population.

Additionally, studies published earlier this year in Toxics and Environmental Sciences Europe found increased instances of cancer, including liver cancer, as well as endocrine disruption and metabolic disorders via inducement of oxidative stress from chronic exposure to 2,4-D.

A troubling trend found in a separate study published in Global Pediatric Health found that young people are facing an unprecedented rise in liver disorders and metabolic syndrome. Tracking the latest science, particularly regarding pesticide exposure and chemical mixtures, can help bridge the existing research gaps.

Regarding dicamba, exposure to the toxic herbicide has been linked to various cancers according to a 2020 research study published by the National Institute of Health in the International Journal of Epidemiology.

Dicamba has also been linked to neurotoxicity, birth defects and kidney and liver damage, not to mention posing harm to birds, fish and other aquatic organisms, according to various peer-reviewed studies identified in the Gateway on Pesticide Hazards and Safe Pest Management webpage.

Dicamba also causes serious damage to non-genetically engineered (GE), non-target plants, damaging habitat and food sources for various organisms, especially for birds, according to fieldwork by Audubon of Arkansas.

See Daily News sections on dicamba and 2-4,D to learn more about the latest regulatory decisions and scientific literature pertaining to the two toxic pesticides.

There has been a flurry of litigation, industry reaction and corresponding actions by the U.S. Environmental Protection Agency (EPA) on dicamba since dicamba-tolerant soybeans and corn entered the domestic market back in 2016 when the EPA initially registered dicamba-based products such as Xtendimax.

In 2020, the 9th Circuit U.S. Court of Appeals nullified “EPA’s 2018 conditional registration of three dicamba weedkiller products for use on an estimated 60 million acres of DT (dicamba-tolerant through GE) soybeans and cotton,” finding that EPA did not adequately consider adverse health effects from over-the-top spraying of dicamba in approving its conditional registration.

Again, earlier this year in February, the U.S. District Court for the District of Arizona rendered moot the EPA’s 2021 approval of three dicamba-based herbicides after a damning Inspector General Report called out EPA’s violation of both the Endangered Species Act and Federal Insecticide, Fungicide, and Rodenticide Act and the agency’s failure to appropriately manage resistance and the devasting impact this failure has on farmers’ livelihoods.

For context, according to the U.S. Department of Agriculture, data gathered in 2018 and analyzed by the Center for Food Safety, “As much as 1 in every 6 acres of ultra-sensitive soybeans were injured by dicamba drift in 2018 alone, over 15 million acres.”

In spite of these developments, the EPA announced an existing stock order permitting the use of dicamba products for the 2024 growing season just a few weeks after this most recent court ruling.

The latest action regarding dicamba is the proposed registration of a new dicamba-based product for GE cotton and soybean crops with a 60-day public comment period that ends on June 3.

Advocates who champion public health, environmental protections and organic agriculture and land management practices put faith in the decades-long body of scientific literature that demonstrates the adverse health effects of toxic chemicals, substances and chemicals.

In this context, EPA continues to permit the use of toxic pesticides, despite the compounding scientific research that supports Beyond Pesticides’s goal to eliminate toxic petrochemical-based pesticides by 2032 and replace the current system defined by product swapping with one that aligns with the National Organic Program and its National List of Allowed and Prohibited Substances.

[…]

Via https://childrenshealthdefense.org/defender/dicamba-2-4-d-weedkillers-serious-illness-pregnant-women/?utm_id=20240521

The Egyptian Origins of Modern Medicine

The Egyptian Ebers Papyrus, psychiatry, depression etiology 1550 BC

Episode 22 Medicine: the Necessary Art

The History of Ancient Egypt

Professor Robert Brier

Film Review

In ancient Egypt, most physicians (and most scribes) were priests associated with temples. Aside from members of the government bureaucracy, they were the only literate members of Egyptian society. Inhotep, the royal architect who built the first step pyramid (see Sneferu: The First Egyptian Pyramid Builder), was also a physician and subsequently became a god associated with the Greek God Aesculapius. Many physicians belonged to temples dedicated to Tof, who would become the god Hermes in Greek mythology. Isis is also associated with healing and the laying on of hands.

Anubis, The Egyptian death god with dog head &quot; facts, art &amp; meaning

Tof

Sekhmet, a woman with the head of a lioness, was the Egyptian goddess of medicine. According to Egyptian mythology, Ra decided to send Sekhmet to wipe out mankind and Tof (the god with an Ibis head) who invented writing got her drunk so she forgot about destroying humanity.

Sekhmet – Egyptian Lioness Goddess - Symbol Sage

Tof is also associated with healing, known as wab (“purification”) in Egyptian. When Horus the son of Osiris lost his eye in his battle with Set (see The Ancient Egyptian Origin Myth ), Tof restored it by magic. In another myth he saved the infant Horus’s life after he was stung by a scorpion.

Sleeping in the temple at Dendera enabled physicians to dream the solution to your illness. People also sought the water cure (the origin of holy water) there, curing themselves by pouring water over themselves that had dripped over the statue of Horus. The temple the female king Hatsheput built in Thebes had a clinic on the roof and temple inscriptions detail patient experiences.

Exorcism was another common treatment, especially for blindness, which was caused by the gods. Most infections were treated with magic spells. One treatment for plague was to burn the bed linens. The treatment to make an old man a youth again was to give him wrinkle cream.

The skill of Egyptian physicians, frequently sought out by other Mediterranean countries, may have been related to their expertise in mummification. Unlike the ancient Greeks, the Egyptians allowed dissection of the dead.

Medicine was one of the few areas of knowledge preserved on papyri. The Edwin Smith surgical papyrus (from around 1700 BC) deals mainly with trauma (mainly broken bones). It lists 48 types of trauma starting with the head. It explains how to immobilize limbs via splinting, as well a offering a magical treatment (for frontal skull injury): grinding up an ostrich shell and painting your head with it.

The Papyrus Ebers (from around 1500 BC) lists 800 remedies, including rubbing a head injury with fish oil and wrapping a sore foot with a deer skin (because deer are really fast runners).

Film can be viewed free with a library card on Kanopy.

https://www.kanopy.com/en/pukeariki/video/1492791/1492846