Saturday, August 27, 2022

The only school district in the US to require public school covid vaccinations just caved. Muriel Bowser's Washington DC stunt has imploded

The criminal imposition of mandates to force children to get COVID vaccinations was floated in many school districts, especially those on the woke west coast. The reason I say it is criminal is because neither the manufacturers nor the USG are willing to risk being held liable for injuries.  So they have made none of the "licensed" vaccine available, and so while the vaccines are technically licensed for kids 12 and up, it is not possible to procure the licensed product.  So instead kids (and adults) are being injected with the EUA product, which is shielded from virtually all liability.  One hopes fraud will pierce the liability shield, but so far there has not been a single case in which this has happened.

Schools on the west coast that imposed these mandates either withdrew them in the face of legal challenge (LAUSD challenged by the Health Freedom Defense Fund) or announced a year's postponement last spring.

But that did not stop tough girl Muriel Bowser, DC's mayor, from threatening to kick kids out of school as recently as yesterday if they weren't vaccinated. (See below).  She also brought us vaccines for 11 year olds without parental permission.  Where is this sister getting her advice? 

Anyway, maybe she did not like the headline below.  Maybe she was scared of the lawsuits.  Maybe she  just found out the vaccine program was experimental.  Maybe 40% of teens expelled from school did not seem like a winning slogan for her next election.

Whatever it was, yesterday she flipped.  The vaccine mandate to attend public school was postponed till January.  Maybe by then she will have been recalled.  We can only hope.


40 Percent of D.C.'s Black Teens Will Soon Be Barred From School Because They Aren't Vaccinated

Mayor Muriel Bowser and the D.C. Council will force all public school students ages 12 and up to be vaccinated against COVID-19.

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Then, a few hours later, this happened:

 https://wtop.com/dc/2022/08/dc-public-schools-push-back-student-immunization-deadlines/

DC public schools push back student immunization deadlines

D.C. public schools are pushing back enforcement deadlines for students who fail to receive their required vaccinations, including against COVID-19.

According to the new attendance guidelines issued Friday, students age 12 or older will have until Jan. 3, 2023, to have received all the needed doses of a COVID vaccine before facing exclusion from school.

Children in pre-K through fifth grade have until Oct. 11 to complete all their routine pediatric immunizations, while students in sixth through 12th grade have until Nov. 4.

Paul Kihn, the District’s deputy mayor for education, told local school officials in a letter that the staggered approach to enforcement is meant to reduce the number of students who can be excluded from schools at any given time.

Families will be sent notices of noncompliance between one and two months before exclusion, depending on grade level.

The new vaccination deadlines for different age groups, issued on Aug. 26. (Screenshot)

“We have heard from many of you about the challenges of tracking enforcement for COVID-19 vaccinations, particularly given the layered 70-day implementation window since the vaccine for 12 to 15-year-old youth was fully approved by the U.S. Food and Drug Administration in July,” Kihn wrote.

“We hope that the Jan. 3, 2023, date for first exclusions of noncompliant students will give schools and LEAs additional time to prepare and for students to get their COVID-19 vaccinations.”

D.C. Public Schools requires immunization against COVID-19 for school enrollment and attendance from all students of an age where a COVID vaccine has received full FDA approval.

Although COVID vaccines are now available for children older than 6 months through an emergency use authorization, the FDA has only granted full approval for children ages 12 and older as of late August.

In a press briefing, Kihn said the decision gives families with students age 12 and up more time to seek COVID vaccines, with the FDA’s full approval coming just weeks before classes start. Kihn also said schools will make use of the extra time to get their own records in order.

“We are working hard to ensure we’ve got accurate COVID-19 vaccination uploaded in all of our systems,” Kihn said. “Because it’s a newer vaccination, it requires a little more time and operational effort to do that. We want to make sure we’re only excluding students based on accurate information.”

State superintendent of education Christina Grant backed the updated approach.

“We think a family’s primary care provider is the best place for students to receive their annual well-child visit and their immunizations,” Grant said. “We think it’s critically important to ensure that we keep our schools safe open, and that we prevent any emergence of diseases that have proven to be eradicated across the country and in the District.”

Two days to discuss: nothing. There is no human data on how these newly formulated vaccines work

CDC has scheduled its ACIP Advisory Committee meeting for Sept. 1 and 2 to sign off on the new Omicron boosters.

The normal notice was not provided in advance of this meeting.

In accordance with 41 CFR 102-3.150(b), less than 15 calendar days' notice is being given for this meeting due to the exceptional circumstances of the COVID-19 pandemic and rapidly evolving COVID-19 vaccine development and regulatory processes…

Matters To Be Considered: The agenda will include discussions on use of COVID-19 vaccines booster doses. A recommendation vote(s) is scheduled. Agenda items are subject to change as priorities dictate.

Procedure for Oral Public Comment: All persons interested in making an oral public comment during the September 1-2, 2022, ACIP meeting must submit a request at https://www.cdc.gov/​vaccines/​acip/​meetings/​ no later than 11:59 p.m. EDT, August 30, 2022, according to the instructions provided.

What’s the hurry? There is barely any COVID. New cases are at their lowest level in 3 months. ICU cases have been way down for a full 6 months.

While it is legal for FDA to omit convening its advisory committee when it makes an important decision, such as authorizing new boosters—without requiring so much as a phase 1 trial in humans—the ACIP (CDC’s advisory committee on immunization practices) and not the CDC itself makes the vaccine recommendations for the entire United States. Then the CDC Director signs off on them. So CDC could not get around convening this ACIP meeting. FDA isn’t convening one because probably Paul Offit and other members would give FDA a blast of truth about such a bold and reckless move: approving vaccines for widespread use before even the shoddiest Phase 3 trial in humans had been performed.

Last year the Director overruled her advisory committee on the adult boosters. Which is unheard of. Rochelle must have been getting her marching orders from God, no Fauci, no Schwab or whoever gives the Great Reset orders, I guess.

So, this is a tricky situation for the ACIP and the Rochelle windup doll. The USG has already ordered about 180 million doses from Pfizer, and some unknown amount from Moderna. So the rollout plan has to be approved by the ACIP Committee.

Last time this happened, the federal government announced its purchase of boosters the day after the FDA advisory committee met. When committee member Paul Offit was later interviewed by Z-Dogg, Offit described the meeting, then the booster vaccine purchase announced the next day, and Offit told Z-Dogg, “The Fix Was In.”

He also told Z-Dogg how it took 20 years to develop the rotavirus vaccine, and then how “nauseating” it was when it rolled out, wondering what side effects it might cause (minute 46). 

This time, the bold and the reckless Biden flunkies didn’t even wait for the meeting to be held, and pre-bought the vaccine ahead of time. If that is not signalling to the members how they are expected to vote, I don’t know what is.

Normally the Committee members show extreme docility regarding the votes CDC wants them to take, even if it means lots of babies will die who didn’t need COVID shots in the first place. However, this is the first time in history a totally new vaccine is to be pushed through the ACIP with no human trials. 3 months ago, it had not even been designed.

Flu shots are slightly adjusted each year, and essentially grandfathered in. But they get used in the southern hemisphere first, so the north (us) gets the benefit of essentially six months of trials down under.

But in this case, for the first time in history, the new boosters with mRNA for omicron BA.4/5 plus the old mRNA vaccine formulation have been through no trials at all. Pfizer only applied for the right to perform clinical trials on Monday Aug. 22 and on August 25 said they had not started yet.

So, it is the ACIP that is to be left holding the bag on this one. Will they suck it up and vote yes? Will they bleat a little, then vote yes? Or will they realize they have been positioned to take the fall and actually ponder the meaning of their vote?

I will live blog the ACIP meeting for Children’s Health Defense. Please join me, and let’s do our best to witness what they try to pull off.

I have also applied to speak during the public comment section. Will I be blocked again?

Here is another wrinkle. Four of the 15 ACIP members are supposed to have completed their 4 year terms on June 30, though their names are still listed on the ACIP roster and they were part of a meeting last month. I think they will be gone at the next meeting, and a new group replacing them will have already been vetted to make sure there are no glitches with this upcoming vote. We won’t know who they are, probably, until September 1. Here are the likely departing members:

AULT, Kevin A., MD, FACOG, FIDSA
Professor and Division Director
Department of Obstetrics and Gynecology
University of Kansas Medical Center
Kansas City, KS
Term: 10/26/2018 – 6/30/2022

KOTTON, Camille Nelson, MD, FIDSA, FAST
Clinical Director, Transplant and Immunocompromised Host Infectious Diseases
Infectious Diseases Division, Massachusetts General Hospital
Associate Professor of Medicine, Harvard Medical School
Boston, MA
Term: 12/23/2020 – 6/30/2022

MCNALLY, Veronica V., JD
President and CEO
Franny Strong Foundation
West Bloomfield, Michigan
Term: 10/31/2018 – 6/30/2022

TALBOT, Helen Keipp, MD
Associate Professor of Medicine
Vanderbilt University
Nashville, TN
Term: 10/29/2018 – 6/30/2022

The Israeli Ministry of Health commissioned a study into vaccine side effects. The researchers came back after 6 months and warned them about medical-legal liability./ Etana Hecht

From Etana's Substack:

https://etana.substack.com/p/safe-and-effective-wash-rinse-repeat

The World’s Laboratory

That Albert Bourla, CEO of Pfizer coined Israel as the “world’s laboratory” is by now well known.

By any reasonable definition, one can assume that the world’s laboratory would be meticulously tracking all vaccine-related data with all the seriousness that a mass medical intervention deserves. Unfortunately at this point, almost two years after the vaccination campaign began, what we look back and find is a dysfunctional mess at the most basic levels.

Let’s begin with December 2020. The vaccination campaign began in Israel, followed closely by the rest of the world, with the elderly, at risk, and healthcare workers. The general population followed at a rapid rate. Throughout that entire first year, the most basic assumption should be that any negative outcomes from the vaccination campaign would be followed closely, with reports of adverse events taken extremely seriously, and meticulously recorded. After all, the rest of the world and Pfizer itself are relying on our data, are they not?

Well, if they were, they didn’t have much to work with. For almost the entirety of 2021, there was no functional central reporting system in place in Israel. There was a form one could send in anonymously, with no way to be tracked or contacted. At the same time, social media was getting flooded with personal testimonies of women who were suffering menstrual irregularities since vaccination. Not only was that signal not taken seriously, but the Israeli Ministry of Health (MOH) deleted thousands of comments of people suffering post-vaccination from a Facebook post of theirs. Thankfully someone archived it so the comments will live on. Just so we remember why we’re fighting so hard to reveal what went on behind the scenes, this is one tiny snapshot from thousands of similar comments back in Oct 2021 (auto-translated from Hebrew):

Finally, at the end of 2021, the MOH quietly released a new system for reporting adverse events post-vaccination, and simultaneously commissioned Professor Mati Berkowitz, a leading Israeli expert on pharmacology and toxicology from Asaf Harofe hospital, to form a team to conduct a study into the adverse event reporting system for the following 6 months as reports came in.

That study concluded in May 2022, and the story surrounding the results of the study itself, the reaction to the results by the MOH, the internal conversation between the research team and the MOH, and the manner in which they presented it to the public is deeply concerning. The various pieces of this story were researched, put together, and released by Israeli journalist Yaffa Shir-Raz and Professor Retsef Levi from MIT, an expert in health systems and risk management and a member of the Israel Public Emergency Council for the COVID 19 Crisis.

Research Team Presents

In early June 2022, there was a Zoom meeting conducted between high-ranking officials at the MOH, and Professor Berkowitz with members of his team. The meeting was to discuss the results of the study, and how to move forward. An unknown source leaked a recording of the zoom, and though it may raise more questions than it answers, the public deserves to know what was truly found in the report, and how the MOH manipulated both data and language to present it to the public.

Yaffa and Professor Levi analyzed the report and the Zoom call, and discovered the following disturbing outcomes:

  • The report and the findings from the report were withheld from the public by the MOH for 2 months. It was released at the beginning of August.

  • As mentioned above, the adverse events reports analyzed were collected beginning 12 months after vaccination, for 6 months. What the MOH then did with the results presented to them by the researchers was calculate rates of adverse events using a denominator of TOTAL vaccines administered, which is about 18 million. The majority of the population got vaccinated with 2 or 3 doses prior to the launch of the reporting system, which means the adverse events in the reports are representative of a very small portion of injections, yet presented as though it’s a comprehensive study of the vaccination campaign.

  • Missing from the report is the size of the population that was studied. The report indicates that this is a report done on the general population, but in reality, it only covers ~15% of the Israeli population. There are 4 main Health Maintenance Organizations, and every Israeli is a member of one of them. Only one of those HMOs, called Meuhedet, complied with the request to hand over the data collected by the reports. Again, using the denominator of all doses given, the MOH didn’t include 85% of reports in their equation.

    Example: As you can see from the report itself, they refer to 18+ million doses administered. The adverse event reports that they studied numbered 8,000+, and they verified 6259 separate events. This represents the rate of adverse events to come from those numbers, however, the 6259 is only representing reports that came in beginning ONE YEAR after the launch of the vaccination, and of those, it only represents about 15% of the reports, from the one health clinic that cooperated and shared their data. With that information in mind, 6259 represents a far greater rate of adverse events than is presented.

  • Contrary to endlessly repeated claims by Pfizer and the MOH that there aren’t serious side effects, and side effects that do occur are short-lasting, the report doesn’t reflect that at all. They define “short-term” as lasting a few days, but 90% of the reports showed effects lasting up to 3 months, with 60% of the reports lasting longer than 3 months, some of them still ongoing.

  • The approval to vaccinate babies ages 6 months through 4 years came three weeks AFTER the report was submitted to the MOH. The MOH did NOT disclose the findings of the report to the committee tasked with approving the vaccine for babies.

Zoom Leaks

The video clips that have been leaked from the Zoom meeting are damning.

Part 1- Rechallenge

Professor Berkowitz can be heard discussing the concept of “rechallenge”. This is a method that proves causation between 2 events, when the reaction to an intervention re-occurs or worsens with another dose. It proves that the reaction was caused by the dose, and was not coincidental. There was a high rate of dose dependent adverse events, and the study proved causation. (The video itself has English subtitles)

Part 2- Medical-Legal Liability

In this clip, Professor Berkowitz discusses the legal liability of the Ministry of Health. Translated from Hebrew, the quote is:

“Here we will have to really think medical-legal. Why medical-legal? Because for quite a few adverse events we said: 'OK, it exists, and there is a report, but still get vaccinated'. I mean, we have to think about how to write it and how to present it correctly. So this will not yield lawsuits later: 'Wait, wait, wait, you said everything will pass and you can get vaccinated. And now look what happened to me. The phenomenon continues.”

Part 3- How Many Men Suffered Menstrual Irregularities?

If the above findings weren't as absurd as they are, I might not believe this next part. In their infinite wisdom, the MOH thought they could get away with calculating the denominator of vaccines against the reports of menstrual irregularities using the total number of adult injections. Adult. Not women. Adult. This means that men were included in the equation of how common menstrual irregularities were.

Besides their brilliance in completely messing up any semblance of a proper calculation, this video clip from the zoom is a team member explaining that they proved causality between menstrual irregularities and vaccination due to re-challenge, and that most of the reports (90%) reported long lasting irregularities.

Logic dictates that if they weren't aware of a connection between menstrual irregularities and vaccination, then they're also not aware of if or how that will affect female fertility. Yet, if we take a look at the official MOH website, the "safe and effective" narrative is still the party line, even for pregnant women. The same Professor Mati Berkowitz who conducted this research report is a signature on this report that states the Covid vaccine is safe for pregnant women.

True Journalism

This all adds to the mounting pile of evidence, anecdotes, data, and testimony for the claim that the Covid vaccines are much more harmful than they were advertised to be.

For a comprehensive conversation about these findings, please watch this interview by Ilana Rachel Daniel at Children’s Health Defense TV.

I’ve only recently begun to appreciate the role that true journalism plays on behalf of citizens. Our job as citizens who were wronged by our governments and medical establishments is to keep looking for the truth and sharing it widely. One day the work of true journalists like Yaffa Shir-Raz will hold to account those who far overstepped their boundaries in our lives.

Thursday, August 25, 2022

No clinical trials. No advisory committee. Newly formulated boosters to be injected starting in 10 days !?!

FDA Plans to Approve Omicron-Targeting Booster Vaccines

Pfizer-BioNTech and Moderna have developed new booster shots optimized for Omicron. They could be approved as soon as Labor Day.

Pfizer-BioNTech and Moderna have developed new booster shots optimized for Omicron. They could be approved as soon as Labor Day.

The Food and Drug Administration (FDA) will likely authorize new Pfizer-BioNTech and Moderna vaccine boosters, updated to combat the emerging COVID-19 variants.

Both mRNA vaccine manufacturers submitted their bivalent booster vaccine candidates to the FDA for Emergency Use Authorization (EUA). The Moderna and Pfizer-BioNTech bivalent boosters are both designed to target the Omicron BA.4/BA.5 and original wild-type COVID-19 strains.

As COVID-19 mutates, it has become more resistant to the vaccines intended to combat its earliest iteration. Additionally, the COVID-19 vaccines naturally wane over time. The highly infectious BA.5 variant is now responsible for an estimated 90% of COVID-19 cases in the United States. This has motivated Pfizer-BioNTech and Moderna to rapidly produce “new and improved” boosters; the BA.5 variant only emerged in June 2022.

Moderna’s EUA seeks approval to administer the updated booster to adults 18 years and older. Pfizer-BioNTech filed their EUA for persons 12 years and older.

Notably, the FDA’s Vaccine and Related Biological Products Advisory Committee (VRBPAC) is not expected to convene and offer a recommendation on the EUAs. If the FDA authorizes these boosters, as the agency is expected to do, the decision will then go to the US Centers for Disease Control and Prevention (CDC).

The CDC’s Advisory Committee on Immunization Practices (ACIP) will convene on September 1 and 2, after which CDC Director Rochelle Walensky, MD, MPH, must sign off on the updated boosters.

Pfizer-BioNTech and Moderna have presented positive data of these new boosters in animal models, human studies have not been completed.  [Have they even started yet?]

If Walensky does approve the new Omicron boosters after next week’s meeting, the shots could be rolled out within a couple days of Labor Day.

What a difference a month makes: WHO tells the press some truth today about the monkeypox vaccines

The story is evolving.  First the Jynneos vaccine was 85% effective.  (Maybe they meant effective at causing cardiac inflammation?)

Today at its press conference, the WHO dropped a truth bomb.  Dr. Kate O'Brien, Director of Immunizations at the WHO, said she wanted to emphasize the following about the monkeypox vaccines:

"We don't have a substantial amount of information about what their performance is."

Does that mean we will soon learn they don't work at all?

Timeline with Terry: my interview with Terry Gilberg

https://ctva.tv/watch-on-demand-below/?video_id=58351&title=TIMELINE%20with%20TERRY%20-%20Guest%20Dr.%20Meryl%20Nass

Monday, August 22, 2022

CDC inexplicably deletes and changes another metric, after disingenuously promising improved transparency.

The NY Times has published a graphic with 4 separate graphs on it daily, since close to the start of the pandemic.  It received all the information in the graphs (and probably the graphics themselves) from the CDC.

The graphs provided the number of cases, ordinary hospitalizations, tests performed and deaths.

Months ago, a useful metric was added:  ICU admissions, which helps define the severity of the current variant.

The third graph in the set showed the number of tests performed daily.  This was useful information, because the number of positive cases was usually directly related, to an extent, to the number of tests.  One could see that by testing more, you upped the number of cases.  When tests were easily available, more tests were done.  When test centers closed, the would be fewer cases reported.

Well, the number of tests performed daily is gone.  Now we have a different graph, which is % positivity on tests.

This is also useful information, but should not have supplanted the number of tests performed.  It would have complemented the number of tests performed.

% positivity essentially tracks the case waves, while the number of tests done suggests to what extent test availability influences the number of cases.

These graphs are particularly important because they encompass the period of time since the start of the pandemic, allowing clear comparisons with other dates since the start of the pandemic.


Now that CDC admitted it has neither been nimble nor transparent with its data and analyses, and claims it will now do better, why have CDC and the Times removed a crucial metric that allowed us to better understand each COVID wave and variant?

Saturday, August 20, 2022

Vera Sharav: “Unless All of Us Resist, Never Again is Now” – Full Speech – Nuremberg, August 20, 2022

https://childrenshealthdefense.eu/eu-issues/vera-sharav-unless-all-of-us-resist-never-again-is-now-75th-anniversary-of-the-nuremberg-code/

My good friend Vera Sharav's speech today at the 75th Anniversary of the Nuremberg Code, Nuremberg, Germany

----------------------------------------------------------------------------------

I came to Nuremberg to provide historical context to the current global threat confronting our civilization. These past 2 1⁄2 years have been especially stressful— as painful memories were rekindled.

In 1941, I was 31⁄2 when my family was forced from our home in Romania & deported to Ukraine.

We were herded into a concentration camp – essentially left to starve. Death was ever-present. My father died of typhus when I was five.

In 1944, as the Final Solution was being aggressively implemented, Romania retreated from its alliance with Nazi Germany. The government permitted several hundred Jewish orphans under the age of 12 to return to Romania. I was not an orphan; my mother lied to save my life.

I boarded a cattle car train – the same train that continued to transport Jews to the death camps – even as Germany was losing the war.

Four years elapsed before I was reunited with my mother.

———————

The Holocaust serves as the archetypal symbol of unmitigated evil

– Moral norms & human values were systematically obliterated.
– The Nazi system destroyed the social conscience.
– Millions of people were worked to death as Slave laborers.
– Others were abused
as experimental human guinea pigs.

The Holocaust did not begin in the gas chambers of Auschwitz and Treblinka.
The Holocaust was preceded by 9 years of incremental restrictions on personal freedom, & the suspension of legal rights and civil rights.

The stage was set by fear-mongering & hate-mongering propaganda.

A series of humiliating discriminatory government edicts demonized Jews as “spreaders of disease.” We were compared to lice.

———————

The real viral disease that infected Nazi Germany is Eugenics— Eugenics is the elitist ideology at the root of all genocides.

– Eugenics is cloaked in a mantle of pseudo- science.
– It was embraced by the academic & medical establishment as well as the judiciary — in Germany and the United States.
– Eugenicists justify social & economic inequality.
They legitimize discrimination, apartheid, sterilization, euthanasia, and genocide. The Nazis called it “ethnic cleansing” — for the protection of the gene pool.
Medicine was perverted from its healing mission & was weaponized.
First, it was to control reproduction through forced sterilization; then it was to eliminate those deemed to be “sub-human” —Untermenschen. The first victims of medical murder were 1,000

German disabled infants and toddlers. This murderous operation was expanded to an estimated 10,000 children up to age 17.
The next victims were the mentally ill; they were followed by the elderly in nursing homes. All of these human beings were condemned as “worthless eaters”.
Under Operation T-4, designated hospitals became killing stations where various extermination methods were tested – including Zyclon B — the gas that was used in the death camps.

———————

The objective of the Nazi Final Solution was to annihilate the entire 11 million Jewish Population of Europe as quickly and efficiently as possible.
The Nazis enacted discriminatory laws; they utilized modern technology; low-cost industrial methods; an efficient transportation system; & a highly trained bureaucracy that coordinated the industrial genocidal process. The objective was high speed, maximum efficiency at lowest cost.

The human casualties of this unprecedented genocide were 6 million Jews & 9 million other people whom the Nazis dehumanized as Untermenschen.
The purpose of Holocaust memorials is to warn and inform future generations about how an enlightened, civilized society can be transformed into a genocidal universe ruled by absolute moral depravity.
If we are to avert another Holocaust, we must identify ominous current parallels before they poison the fabric of society.
Since the Nazi era, the study of history & most of the humanities—including philosophy, religion, and ethics — have been overshadowed by an emphasis on utilitarian science & technology.
As a result, few people recognize foreboding similarities between current policies & those under the Nazi regime.
By declaring a state of emergency—in 1933 & in 2020, constitutionally protected personal freedom, legal rights, and civil rights were swept aside. Repressive, discriminatory decrees followed.

In 1933, the primary target for discrimination were Jews; today, the target is people who refuse to be injected with experimental, genetically engineered vaccines. Then and now, government dictates were crafted to eliminate segments of the population.

In 2020, government dictates forbade hospitals from treating the elderly in nursing homes. The result was mass murder.
Government decrees continue to forbid doctors to prescribe life-saving, FDA approved medicines; government-dictated protocols continue to kill.

The media is silent – as it was then.
The media broadcasts a single, government-dictated narrative – just as it had under the Nazis. Strict censorship silences opposing views.
In Nazi Germany few individuals objected; those who did were imprisoned in concentration camps.

Today, doctors & scientists who challenge the approved narrative are maligned; their reputations trashed. They risk losing their license to practice as well as having their homes & workplace raided by SWAT teams.

———————

The moral significance of the Nuremberg Code cannot be overstated:

The Nuremberg Code is the most authoritative, internationally recognized document in the history of medical ethics.

This landmark document was formulated in response to the evidence of medical atrocities committed by Nazi physicians and scientists.

The Code sets forth moral boundaries for research involving human beings.

The Nuremberg Code rejects the ideology of Eugenics & unequivocally asserts the primacy & dignity of the individual human being – as opposed to “the greater good of society.

American jurists who formulated the Nuremberg Code incorporated the official 1931 German “Guidelines for Human Experimentation” authored by Dr. Julius Moses. Those Guidelines remained legally in force until 1945. The Nazis violated them in their entirety. Dr. Moses, who was Jewish, was deported to Theresienstadt where he died.

———————

The Nuremberg Code defined foundational, universal moral and legal standards; affirming fundamental human rights.

These human rights apply to every human being.

– The Code sets limits on the parameters of permissible medical experiments.
– Equally important, the Nuremberg Code holds doctors and research investigators personally responsible to ensure the human subjects’ safety & to ensure that the person freely gave his voluntary, fully informed consent. The standards of the Nuremberg Code are incorporated in the International Criminal Code. They are legally applicable today in peacetime & during war.

The objective of the Nuremberg Code is to ensure that medicine, never again deviates from the precautionary ethical principle, “First, do no harm.

The Nuremberg Code has served as a blueprint for subsequent national and international codes of human rights – to ensure that:
– the rights & dignity of human beings are upheld;
– & to ensure that medical doctors never again engage in morally abhorrent experiments.
– Like the 10 Commandments, not a word of the Code may ever be changed.

The first of 10 ethical principles lays down the foremost ethical requirement – which is spelled out in great detail:

The voluntary consent of the human subject is absolutely essential”.

This means that the person involved should have legal capacity to give consent; should be so situated as to be able to exercise free power of choice, without the intervention of any element of force… constraint or coercion; and should have sufficient knowledge & comprehension of the elements of the subject matter involved as to enable him to make an understanding and enlightened decision. This… requires that before the acceptance… of an affirmative decision by the experimental subject… [he] should be [informed of] the nature, duration, and purpose of the experiment; the method and means by which it is to be conducted; all inconveniences & hazards reasonably to be expected; and the effects upon his health or person which may possibly come from his participation in the experiment.
The duty and responsibility for ascertaining the quality of the consent rests upon each individual who initiates, directs or engages in the experiment. It is a personal duty & responsibility which may not be delegated to another with impunity.

———————

The genocidal culture that permeated the Nazi regime did not end in 1945. It metastasized in the United States.

At the end of the war, US government agents helped 1,600 high ranking Nazi scientists, doctors, & engineers to evade justice at Nuremberg.

These Nazi technocrats facilitated the murderous Nazi operations. They were Hitler’s partners in crimes against humanity. They were secretly smuggled into the US under Operation Paperclip. This was in violation of explicit orders by President Harry Truman. These Nazi criminals were placed in high-level positions at major American scientific & medical institutions where they continued their work.

What’s more, these Nazi technocrats trained a generation of American scientists, doctors, & engineers.
This is how Nazi methods, & the immoral disregard for human values were entrenched in America.

In 1961, in his farewell address to the nation, President Dwight Eisenhower warned against the increasing dominance of “the military-industrial complex” whose “total influence – economic, political, even spiritual – is felt [everywhere]

Eisenhower warned: “we must be alert to the danger that public policy could itself become the captive of a scientific-technological elite.

In 1979, a report to the President, by the US Commission on the Holocaust, chaired by Auschwitz survivor Elie Wiesel warned:
…the inclination to duplicate the Nazi option and once again to exterminate millions of people remains a hideous threat.”

Those who declare that Holocaust analogies are “off limits”—are betraying the victims of the Holocaust by denying the relevance of the Holocaust.

The Nuremberg Code has served as the foundation for ethical clinical research since its publication 75 years ago.

The Covid pandemic is being exploited as an opportunity to overturn the moral and legal parameters laid down by the Nuremberg Code.

The Nuremberg Code is our defense against abusive experimentation.

———————

Humanity is currently under siege by the global heirs of the Nazis.

A posse of ruthless, interconnected, global billionaires have gained control over national & international policy-setting institutions.

They have embarked on implementing a diabolical agenda:
– Overthrow democracy & Western civilization;
– Depopulate the global population;
– Eliminate nation-states & establish One World Government;
– Eliminate cash & establish one digital currency;
– Inject digital IDs & artificial intelligence capabilities into every Human being. If these objectives become a reality, we will be digitally surveilled 24 hours a day, 7 days a week.

In May 2022, at the World Economic Forum in Davos, Klaus Schwab, the architect of the dystopian Great Reset declared:
“Let’s be clear, the future is not just happening; the future is built by us, a powerful community here in this room. We have the means to impose the state of the world.”

The ultimate goal of these megalomaniacs is to gain total control of the worlds’ natural resources, financial resources and to replace humans with Transhuman robots.

[1] Transhumanism is a bio-tech- enhanced caste system – the New Eugenics.

Klaus Schwab’s lead advisor is Yuval Noah Harari, an Oxford University trained, Israeli. Harari is a proponent of the New Eugenics & Transhumanism.

Harari refers to humans as “hackable animals” He declared: “We have the technology to hack humans on a massive scale…

Harari despises the very concept of God.

Transhumanists despise human values, & deny the existence of a human soul. Harari declares that there are too many “useless people.” The Nazi term was “worthless eaters

This is the New Eugenics.
It is embraced by the most powerful global billionaire technocrats who gather at Davos: Big Tech, Big Pharma, the financial oligarchs, academics, government leaders & the military industrial complex. These megalomaniacs have paved the road to another Holocaust.

This time, the threat of genocide is Global in scale.

This time instead of Zyklon B gas, the weapons of mass destruction are genetically engineered injectable bioweapons masquerading as vaccines.

This time, there will be no rescuers. Unless All of Us Resist, Never Again is Now.

———————

Vera Sharav
Holocaust Survivor
Public Advocate for Human Rights
Founder and President of the Alliance for Human Research Protection (AHRP)

Monkeypox virus: some truth about the virus and the horribly false solution

Monkeypox is a real virus that spreads due to skin contact, almost exclusively. If you don’t want to call it a virus, that is okay with me. It is a contagious something that spreads person to person or rarely between animals and humans. If you are not in really closely contact with someone while they are harboring a replicating virus, you won’t get it. Okay, sheets and towels and [smallpox] blankets might spread it, based on experience with smallpox.

The CDC wants to reinvent itself so we can all trust it again. This would require it to produce guidance that is helpful, not harmful, and to be truthful—which it has been unable to do so far, and I don’t think it knows how.

But I can remind the CDC how to make itself useful. Remember the AIDS epidemic, Tony and Rochelle? Aren’t you both supposed to be among America’s top experts on AIDS? That’s your specialty, right?

When NYC faced an HIV epidemic, it closed the bathhouses. It didn’t raise the status of its equity office, Rochelle. Simple, but it made a difference.

Monkeypox is a mild disease but the “pocks” are a great annoyance, because we hate seeing and dealing with them. In some areas, like the mouth and private parts, their downstream effects can be rather painful. The pocks may result in scarring.

Let’s face it: we don’t like dealing with pocks, especially the majority of us who always want to look good. And so the media have taken our distaste and projected it back to us, making the illness appear a lot worse than it actually is. Most cases have only had a few pocks.

The disease (open pocks) lasts from 1-4 weeks. The viral syndrome (fever, malaise) only lasts a few days. CDC said to its ACIP Advisory Committee on June 24 that only symptomatic care is generally needed, and I think that is correct: drink fluids, rest. I don’t think they necessarily want the rest of the population to know that.

I think my case of measles around age 7 was probably worse—I had the things in my mouth and all over my body and eating and drinking was painful and I felt miserable. Here is what my measles looked like:

I am not sure how long people remain contagious with monkeypox; our public health officials have not informed us yet. From UptoDate:

until the 2022 outbreak, transmission outside of a household and sustained human-to-human spread had been rare….Viral shedding and period of infectiousness — A person is considered infectious from the onset of clinical manifestations until all skin lesions have scabbed over and re-epithelialization has occurred.

A report of seven cases in the United Kingdom between 2018 and 2021 demonstrated polymerase chain reaction (PCR) positivity in blood and upper respiratory tract samples for at least three weeks in three of the patients. However, it is not clear what this means with respect to infectivity, and the correlation of PCR and culture positivity was not described in the report. Thus, PCR testing of throat or blood samples is generally not done for clinical decision making, and the duration of isolation is determined by clinical evaluation.

Which means, treat the lesions like we treat shingles, cause we don’t really know the duration of contagiousness. If they told us you stop being infectious after a few days or a week, it would seem milder, and the powers that be don’t seem to want that.

Instead the PTB and media are really milking it. For example, writing in depth articles about this serious threat to the nation. Like this one from the WaPo, which is desperately helping the USG to stay on top of the narrative, after I and perhaps others spilled the beans about how much vaccine the USG actually owns. (16 million doses, they say, but it could be more, despending how much has been trashed.) My guess is none has been destroyed and we probably have 30-40 million full doses, some of which may have expired. Sitting frozen in Denmark, hidden from view. Excerpts from the in depth article of August 17 are below, with commentary:

Chaplin [CEO of the Jynneos manufacturer] threatened to cancel all future vaccine orders from the United States, throwing into doubt the administration’s entire monkeypox strategy.

“People are begging for monkeypox vaccines, and we’ve just pissed off the one manufacturer,” said one official who spoke on the condition of anonymity because they were not authorized to comment.

Juice up the story by creating a fake conflict. Make sure it hints of future shortages. CYA by making it anonymous. BTW, this WaPo article includes 3 videos of three gay men showing off their lesions. Because the Yuck! factor is critical to sell the vaccines.

a plodding bureaucracy left hundreds of thousands of gay men facing the threat of an agonizing illness

Nobody has died after 10,000 US cases identified, so it better at least be agonizing. Occasionally.

Demetre Daskalakis, a senior official at the Centers for Disease Control and Prevention, was working from home on HIV prevention projects over the May 14 weekend when CDC colleagues summoned him to an urgent call as cases of unusual lesions had begun to appear in Britain.

Daskalakis quickly brushed up on the symptoms and origins of monkeypox.

“I did the yeoman’s work of getting my infectious-disease biology textbook out and just reviewing stuff about monkeypox to be ready,” Daskalakis said.

Are you impressed? Senior CDC official reads a few paragraphs in a textbook to bone up on monkeypox. What about reading the original literature, bonehead, so you actually might know something, given your responsibility for the entire country’s response?

I have to tell you, I was at a discussion of anthrax about 20-25 years ago with scientists from Fort Detrick and CDC scientists (CDC made the decisions about handling the anthrax letters response). David Ashford and Art Friedlander were there. The CDC people were ignorant about anthrax then; they never had bothered to read the primary literature. That’s why CDC let people keep working in the AMI building in Florida for several days after anthrax was discovered, and minimized the risk to postal workers.

Some things never change.

At the time, the national emergency stockpile held 2,400 doses of Bavarian Nordic’s Jynneos, the only vaccine approved by the Food and Drug Administration for monkeypox. While the United States had purchased millions more potential doses, they sat in Bavarian Nordic’s factory in Denmark, either as finished doses in freezers or as raw materials, waiting to be turned into vaccines.

The U.S. stockpile also had hundreds of millions of shots of an older vaccine approved for the related smallpox virus, ACAM2000, although health officials were wary of using that vaccine — given the increased risk of side effects and even inadvertent illnesses — and considered it a fallback.

But the Jynneos doses in the stockpile were losing shelf life because its freezers were capable of storing the doses only at negative 20 degrees Celsius, while Bavarian Nordic’s freezers in Denmark kept doses stored at negative 50 degrees Celsius.

Before, the media and CDC said the ACAM-2000 stockpile was “at least 100 million.” After I pointed out we bought 300 million doses back in the early 2000s and plenty more since, the story got updated to hundreds of millions. The ACAM-2000 production company is now under the ownership of the anthrax vaccine manufacturer, Emergent BioSolutions. Which means there will be no quality control on vaccine production. This company had to throw away nearly 400 million COVID vaccine doses due to contamination. The taxpayer’s loss. Congress said so

Committees’ Report on Emergent BioSolutions Uncovers Extensive Vaccine Manufacturing Failures, Deliberate Efforts to Hide Deficiencies.  May 10, 2022

Okay, so the US had already spent around $1.6 billion on the Jynneos vaccine, intended mainly for smallpox, before monkeypox showed up in May. The company had been producing doses for the USG since 2013 or a bit earlier. But the WaPo, the USG mouthpiece, is hinting to us that the government was too cheap to buy the necessary freezers to store it, and that is the excuse why they have been sitting in Denmark? AYFKM?

No, they weren’t kidding.

Shipping the doses would create additional challenges in keeping the vaccines as cold as possible for their 4,000-mile voyage to the United States.

“Every time we move doses from their freezer to the [stockpile] … we lose two years of shelf life,” said Dawn O’Connell, head of the Administration for Strategic Preparedness and Response, which oversees the national stockpile. “Every time we convert doses from [raw materials] to a vial, we lose seven years of shelf life.”

Wait, what? Nearly the entire stockpile of tens of millions of doses has been produced in the past 9 years, and Assistant Secretary of HHS O’Connell just talked about them losing 9 years of shelf life when they get shipped and bottled. Sounds like they must be starting with more than 9 years of shelf life at minus 50 C. Which suggests virtually none of the stockpile expired, after earlier claims that 20 million doses had expired.

Didn’t the USG know this before spending $1.6 Billion to have them manufactured and stored in bulk in Denmark?

Wasn’t the purpose to buy this huge stockpile of vaccine in case of a smallpox emergency? Don’t you need to get it over here pronto when that happens? Like yesterday? Who is blowing smoke by implying there was no plan to rush this stuff from Denmark into arms in days or at most a few weeks, had smallpox occurred?

Early on, every monkeypox test required physicians to first get permission from a city or state epidemiologist, often an hours-long process that required multiple phone calls or emails — before the sample was sent to a public health laboratory, which could take days to release results.

Just like at the start of COVID, CDC controlled all US monkeypox testing. [I don’t know why they did this, but this is one way to control the number of reported cases. And maybe to let it spread more?] Only CDC had the test, and it wasn’t until around July 1 that CDC shipped tests to public health labs and commercial labs and allowed them to do testing as well.

The restrictions created a chokehold: Only about a dozen tests per day were being performed nationwide in early June, at a time when officials believed hundreds or thousands of daily tests were needed to detect infection clusters and head off an outbreak.

Sound familiar?

And communicating the risks of monkeypox to the public was proving to be a challenge, with officials struggling to warn the gay men who were disproportionately contracting the virus, often through sex with multiple partners, while not stigmatizing them.

This stigmatizing BS is a bad joke. Public health officials have been doing contact tracing for syphilis, for example, forever. No one ever said it would stigmatize the polyamorous, or sex workers. All the data are supposed to be strictly confidential. It’s what you do to save lives and prevent fetal malformations. Warn those at risk, dammit. Don’t stigmatize them. Inform them. Keep it confidential. You already have the syphilis protocols and know how to do this. Stop playing coy. Couldn’t CDC come up with a better excuse for not doing its job?

The job today: explain the nation’s plan to split vaccine doses in fifths and administer them with a new injection method, transforming about 441,000 doses of Jynneos into more than 2 million potential shots. The plan was finalized by the FDA over the pharmaceutical company’s safety concerns and after the company backed away from its CEO’s threat to cancel future orders.

So we are ‘unable’ to quickly get the Denmark 16 plus millions of doses shipped and bottled for use. The vaccine is fully licensed and legally could very well have liability attached to it if injuries occur (and plenty will-I previously wrote about very high numbers of recipients in the clinical trials with elevated cardiac enzymes and worsening HIV status). Hello Rochelle and Tony, was this deliberate? Instead of worrying about stigmatizing, are you warning HIV positive people that the vaccine is known to cause higher HIV virus titers and lower CD4 counts?

And then there is this: the USG is ‘able’ to get the already bottled doses sucked out of vials, diluted and totally rebottled as diluted product, never having undergone testing of the process, whether it works, whether the dose makes sense. The administration announced it will be doing that, which is not simple.

But they can’t just defrost and bottle the bulk vaccine? Seems to me it is a lot more complicated to remove, dilute and rebottle than to simply bottle what we already own. Especially since we own plenty. Buy the freezers, ship the stuff over, and have US companies bottle it. That is, if we really need it and this whole thing is not a clown show.

The diluted product got an EUA on August 9, which removes essentially all liability. How convenient. Maybe that is why the USG is diluting it? Or will they just bottle the old vaccine, call it diluted, and still get the liability waiver?

BTW, the intradermal injection method is the exact same method used when doing a TB test. Not hard to learn or to do.

So many gay men across the country still struggling to get vaccinated. A second dose needed 28 days after the first shot. At least 14 days after the second dose for full protection.

Full protection? STAT, as I previously noted, recently carried an Op-Ed by 2 former top officials at FDA on the monkeypox vaccines. They revealed that the Jynneos vaccine does not prevent transmission! It supposedly reduces severity of the disease. Except it is mild to begin with.

Where have we heard that before? Go get vaccinated, risk myocarditis or a worsening of HIV, wait 42 days for “full protection” from a diluted dose (or not) that has never been tested in humans—and then find out you can still catch and spread monkeypox.

Fool me once, shame on you. Fool me twice…

UPDATE Aug 20:

Breakthrough monkeypox cases emerge

Preliminary reports on monkeypox vaccinations suggest the vaccine is not 100 percent effective, and some breakthrough cases are occurring, the World Health Organization said during an Aug. 17 media briefing. 

In some cases, breakthrough infections are occurring in people vaccinated after a monkeypox exposure, which is intended to reduce disease severity. The breakthrough cases should not come as a surprise, as the WHO was not expecting 100 percent efficacy, according to Dr. Rosamund Lewis, the organization's technical lead for monkeypox. [Is it a surprise to the gay men lining up for hours for a shot at the shot?—Nass]

"We have known from the beginning that this vaccine would not be a silver bullet, that it would not meet all the expectations that are being put on it, and that we don't have firm efficacy data or effectiveness data in this context," she said.

Dr. Lewis cited a limited study from the 1980s, which showed that smallpox vaccines used at the time were about 85 percent effective against monkeypox. [It used a different vaccine, believed to be much more effective than Jynneos, however.—Nass]

She said it's unclear what the current vaccine's overall efficacy will be, but still stressed the importance of vaccination to protect those at high risk.