DIED SUDDENLY & WAKING THE SHEEPLE

Some people wouldn’t know Tyranny

if it covered their faces,

Locked them in their homes,

Enacted the biggest wealth transfer in History

Censored them

made them show papers

and forcibly injected them

with a slow ‘poison’….

RDS in the following comment points out one of the problems we have in waking up the Sheeple. There are highly ‘respected’ doctors and PhDs, who write papers in prestigious journals backing the mRNA vaccines even though they KNOW they are unsafe.

RDS:

Wolf Moon
OMG, this article below is a must-read. Linked from an AMA EdHub email one received today. It’s a JAMA piece written by Dr. Peter Marks — he’s the head of the CBER department of the FDA (Center for Biologics Evaluation and Research). Dr. Marks was in on the ground floor of Operation Warp Speed. Dr. Marks KNOWS EVERY DATA PIECE SUBMITTED TO THE FDA FROM PFIZER-BIONTECH ABOUT THE CLINICAL TRIALS FOR BNT162b2 BACK IN 2020 — AND EVERY DATA PIECE SINCE THEN ALSO.
Dr. Marks was in on recommending that the FDA authorize the UNPROVEN, ONLY TESTED ON 8 MICE new “COVID-19 + Omicron BA.4 + Omicron BA.5 booster shot.”
His linked article below is a screed for the development of “new” and “different types” of COVID-19 “vaccines” — including ones that specifically target the T-cell response in the body.
Dr. Marks KNEW that the “vaccines” developed during Operation Warp Speed and given quick EUAs by the FDA WOULDN’T DO THE JOB:
From his article:
“One potential model for approaching such development [of a COVID-19 vaccine] was used successfully at the beginning of the pandemic when Operation Warp Speed evaluated numerous global vaccine types and focused on advancing several promising candidates, knowing full well that most would ultimately not be found to meet the criteria set forth for a safe vaccine with adequate efficacy.” (bolding and Italics mine)
Dr. Marks represents the “medical establishment” and DeepState.
IMO, the “medical establishment” and the DeepState have it as their business to continue to put these dangerous COVID-19 “vaccines” into people — and develop new “vaccines” to keep damaging / destroying the immune systems of those who take them.
His article:
https://jamanetwork.com/journals/jama/fullarticle/2799600
December 9, 2022
“Urgent Need for Next-Generation COVID-19 Vaccines”
Peter Marks, MD, PhD
https://www.youtube.com/watch?v=Nat1za4sKjA
As an additional note. For those who might wish to watch the documentary it is available to watch free until the end of January. All that is required is your email I think. The link follows.
https://therealanthonyfaucimovie.com/trailer/

In addition to censorship and smearing of dissenting voices, hospitals and doctors were getting the carrot and stick treatment – Lose your license OR get big bucks for pushing bogus PCR tests, ventilators, Remdesivir and killing patients. – For example “A COVID-19 diagnosis provides extra payments to coroners!”

To make sure the Sheeple could not make a solid connection between the Covid Vaccine and death, the shot is a slow ‘poison’ with a variety of adverse reactions.

Steve Kirsch: Vaccines are taking an average of 5 months to kill people

The CDC has been hiding the Social Security Administration death master file. I got it from a whistleblower. This shows deaths are taking 5 months from the jab to happen. This is why it’s hard to see.

Remember this time factor as we look at the data I found.

Finally we have the DELIBERATELY compromised VAERS system that is SUPPOSED to alert the CDC and FDA to harmful drugs.

Why Did the CDC Silence the Million Dollar Harvard Project Charged With Upgrading Our Vaccine Safety Surveillance System? BY TRUTH SNITCH

NOTE THE DATE! → OCTOBER 24 2017

There are major problems with the vaccine adverse event reporting system (known as VAERS) which the CDC considers the “front line” of vaccine safety. VAERS was created in 1990 by the CDC and FDA as a means to collect and analyze adverse effects that are associated with vaccines. Unfortunately, the failings of VAERS are “kept from the consciousness” not only of the public, but also from the doctors, pediatricians, and nurses that the public rely on to provide reliable information as to the safety of vaccines. I say “kept from the consciousness” rather than “kept secret” because while these failings are publicly disclosed for all the world to see, they are for all intents and purposes BURIED in documents seldom searched out by the average member of the medical community, much less by the average individual. You could say that the information has been very effectively hidden in plain sight…

In 2000, the 6th Report by the Committee on Government Reform addressed the failings of VAERS in its address of the Vaccine Injury Compensation Program…. [The] Congressional report notes (on page 15), “Former FDA commissioner David A. Kessler has estimated that VAERS reports currently represent only a fraction of the serious adverse events.” (emphasis by author)… That leads us to the interesting case of the CDC and Harvard Pilgrim Healthcare Inc.

The Department of Health and Human Services (HHS) gave Harvard Medical School a $1 million dollar grant to track VAERS reporting at Harvard Pilgrim Healthcare for 3 years and to create an automated reporting system which would revolutionize the VAERS reporting system- transforming it from “passive” to “active.”…

I’ll quote the findings directly from the report,

“Adverse events from drugs and vaccines are common, but underreported. […] Likewise, fewer than 1% of vaccine adverse events are reported. Low reporting rates preclude or slow the identification of ‘problem’ drugs and vaccines that endanger public health. New surveillance methods for drug and vaccine adverse effects are needed.”

Again, let’s stop and think about this revelation for a moment: fewer than 1% of vaccine adverse events are reported. The CDC’s entire vaccination propaganda campaign rests on their claim that side effects from vaccination are exceedingly rare (and predominantly minor). According to the CDC, in 2016 alone, VAERS received 59,117 vaccine adverse event reports. Among those reports were 432 deaths, 1,091 permanent disabilities, 4,132 hospitalizations, and 10,274 emergency room visits. What if these numbers actually represent less than 1% of the total as this report asserts? Simple multiplication would yield vaccine adverse events reports numbering 5,911,700!…

the United States of America Centers for Disease Control ghosted Harvard Pilgrim Healthcare, Inc.

For those who are unaware, Google dictionary defines ghosting as,

“the practice of ending a personal relationship by suddenly and without explanation withdrawing from all communication.”

Personally, I would hope that I could hold an organization like the CDC to a higher standard, but… After a one million dollar grant was paid and three years of research conducted on what appeared to be a very successful upgrade to the passive VAERS system, the team’s CDC contacts went MIA

. The ESP:VAERS final report states, “Unfortunately, there was never an opportunity to perform system performance assessments because the necessary CDC contacts were no longer available and the CDC consultants responsible for receiving data were no longer responsive to our multiple requests to proceed with testing and evaluation.”

So in 2017, the CDC DELIBERATELY left a useless reporting system in place when they had the opportunity to upgrade it.

Since the VAERS data set is compromised as well as next to useless, I decided to see if we could find another way to connect the mRNA vaccines to deaths. There is a nifty site called Dead or Kicking.

If you go to https://deadorkicking.com/death-statistics/us/2020/ (Towards the bottom)

there is the graph “United States death comparison by age in 2020“

By changing the date in the URL you get the different years AND if you place your mouse over the graph, it will give you Deaths, Death Rate and Population for each age group.

You can save the graphs for any year – or all of them – as examples, as Wolf did below. Right-clicking on a graph lets you “save image as” or “copy image”.

2019

2020

2021

2022

Note Added By Wolf – CHECK THIS ONE OUT!!!

I originally thought I would see a major drop in the population over 75 but that did not happen since the Baby Boomer cohort is filling the 65+ age groups faster than the orchestrated depopulation can kill them. Notice there are less people in the 45 to 54 age group than in the 55-64 age group. That is a REAL PROBLEM for the Cabal.

Social Security Scam: Where Did the $2.5 Trillion Surplus Go?

July 19 2011

…The Social Security Trust Fund should currently have $2.5 trillion in surplus. So how is it that these checks could stop being issued if the debt ceiling isn’t raised? Economics professor Dr. Allen Smith, author of The Looting of Social Security: How The Government is Draining America’s Retirement Account, has been reporting on the theft of Social Security funds for years….

Age / Date	2019	2020	2021	2022
85+	6,604,958	6,628,013	6,673,175	6,715,875
75-84	15,969,872	16,022,410	16,139,651	16,250,631
65-74	31,483,433	31,571,207	31,773,610	31,970,852
55-64	42,448,537	42,643,579	42,929,850	43,208,648
45-54	40,874,902	41,050,404	41,371,452	41,683,591

So I created another table this time of USA Death Rates by age group by year. I included 6 years before covid as a baseline. Then the two years, 2019 & 2020, when Covid hit the USA plus the two years, 2021 and 2022 when the mRNA vaccine was progressively rolled out, starting with adults, then school age children and finally babies.

Age/Date	2013	2014	2015	2016	2017	2018	2019	2020	2021	2022
85+	136.60	134.08	136.74	133.92	135.74	134.51	132.29	162.24	138.49	120.22
75-84	46.48	45.64	45.79	44.75	44.73	43.86	43.08	52.16	50.33	49.00
65-74	18.02	17.86	17.97	17.89	17.91	17.83	17.65	20.92	22.25	23.96
55-64	8.60	8.70	8.75	8.84	8.86	8.87	8.83	9.86	10.85	12.05
45-54	4.06	4.05	4.04	4.06	4.02	3.96	3.92	4.23	5.08	6.12
35-44	1.72	1.75	1.80	1.92	1.95	1.95	1.99	2.12	2.88	3.92
25-34	1.06	1.08	1.17	1.29	1.33	1.29	1.29	1.37	1.76	2.24
15-24	0.65	0.65	0.70	0.75	0.74	0.70	0.70	0.72	0.86	1.05
5-14	0.13	0.13	0.13	0.13	0.14	0.13	0.13	0.13	0.14	0.14
1-4	0.26	0.24	0.25	0.25	0.24	0.23	0.23	0.23	0.22	0.25
<1	5.95	5.88	5.90	5.83	5.67	5.58	5.53	5.56	4.88	4.39

The following groupings are interesting…..

RETIREES 75+

We know 5 democrat governors forced people with ACTIVE COVID INFECTIONS into nursing homes, killing a lot of the elderly and they were not the only ones. 45% of all US coronavirus deaths occurred in nursing homes.

Also there was the DELIBERATE mis-diagnosis of flu and pneumonia followed by refusal to treat until the person was so sick they needed to be put on a ventilator & remdesivir thus killing up to 88% of those patients.

There was also deferred health care. Study: 4 in 10 U.S. adults deferred medical care due to COVID-19

The result of all of this, is the most vulnerable elderly had already been killed off in 2020 as the much higher death rates for 2020 shows, but by 2021 and 2022 the death rates decrease from that high. Although the elderly were vaccinated, unlike athletes and younger, physically active people, the elderly are going to be a lot more sensitive to what their bodies are telling them and NOT pushing it. They are also more likely to have doctors checking their heart health and be on heart and circulatory medications.

March 2020 Myocarditis in athletes: A clinical perspective

Abstract

Myocarditis is an important cause of arrhythmias and sudden cardiac death (SCD) in both physically active individuals and athletes.

>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>

RETIREES 65 to 74

The 65 to 74 group is going to be a mixed bag. Compared to the 75+ group they are less likely to be in a nursing home or to have gotten deathly ill in 2020, although a certain percentage will have died. However they are likely to get the vaccine. Thanks to Medicare, they are more likely to be in contact with medical professionals who would try to talk them into the jab. They are also going to be a lot more physically active than older retirees and therefore stressing their hearts more after getting the mRNA vaccine.

You can see the combination of poor health care in 2020 followed by the vaccines and then boosters as the death rate increases year by year from 2019 through 2022.

>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>

FORCED RETIREMENT/SMALL BUSINESS WORKERS 45 to 64

The 45 to 64 are an interesting group. Corporations force retirements and actively discriminate against those 45 years and up because age discrimination laws have no real teeth. Therefore the people 45 and up are most likely NOT working for ‘Corporate America’ and are either small business people or hired by small business people. (BTDT) This group is the most likely to have had a ‘rude awaking’ about the world we live in and are NOT going to be as trusting. Older people are also more likely to tell their boss to go F..K themselves with the darn needle. Like the 65 to 75 group you can see the increase in death rate year to year but it is not as sharp an increase. They are also more likely to be in better health than retirees.
If You’re Over 50, Chances Are the Decision to Leave a Job Won’t be Yours
Age discrimination in the workplace happening to people as young as 45: study

>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>

WORKING AGE CORPORATE AMERICA 15 TO 44

The age group 15 to 44 is the group most likely to show PURE UNADULTRATED DATA about Mortality & the mRNA vaccine although there may be some confounding from drug use increasing over the years. Covid-19 virus has little effect on the death rate in 2020. However as the boosters and the 5 month time delay kicks in you can see the death rate almost doubled in 2022 compared to 2019 and earlier.

THIS IS THE GROUP TO WATCH.

JANUARY 3, 2022 – Insurance executive says death rates among working-age people up 40 percent

….Scott Davison, the CEO of OneAmerica, a $100 billion life insurance and retirement company headquartered in Indianapolis.

“The data is consistent across every player in the business.”

Davison said death rates among working age people –

those 18 to 64-years-old – are up 40 percent in the third and fourth quarter of 2021 over pre-pandemic levels.

“Just to give you an idea of how bad that is, a three sigma or 200-year catastrophe would be a 10 percent increase over pre-pandemic levels,” Davison said. “So, 40 percent is just unheard of.”

He blames it on Covid instead of the mRNA vaccine of course. “…the third and fourth quarter of 2021…” would be after Steve Kirsch’s 5 month window. So far I can not find any 2022 insurance data. HMMMmmmm

>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>

CONTROL GROUP 1 TO 14

The 1 year to 14 can be considered the ‘Control Group’ Covid has little if any effect on the death rate in 2020. They were not vaxed until quite recently (November 2021) and boosters were not approved until May 19, 2022. The death rate so far has been flat but I would expect an uptick after the first of this year as the effects of the boosters kick in.

>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>

BABIES UNDER 1 YEAR

The Under one year of age is interesting since there is actually a slight dip in mortality. Are weaker babies more subject to spontaneous aborting after Mom is vaxed?

>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>

TIMELINE of Emergency Use Authorization of mRNA VACCINES

The FDA makes it VERY HARD to figure out just when they authorized the use of the mRNA vaccine in youngsters. I gleaned out the following dates. Starting from the FDA Covid Vaccine site.

Turns out it is the CDC who has the final say on vaccination of children so I have also included the CDC news releases.

12/18/2020 – EUA issued for the Moderna COVID-19 Vaccine, December 18, 2020.
Emergency Use Authorization (EUA) of the Moderna Inc. COVID-19 Vaccine for the prevention of COVID-19 in individuals 18 years and older.

YEAR 2021

06/10/2021 — Vaccines and Related Biological Products Advisory Committee will meet in open session to discuss, in general, data needed to support authorization and/or licensure of COVID-19 vaccines for use in pediatric populations.

FDA DEFINES:
Pediatric use. (A) Pediatric population(s)/pediatric patient(s): For the purposes of paragraphs (c)(9)(iv)(B) through (c)(9)(iv)(H) of this section, the terms pediatric population(s) and pediatric patient(s) are defined as the pediatric age group, from birth to 16 years, including age groups often called neonates, infants, children, and adolescents.

.
09/17/2021 — Application for administration of a third (“booster”) dose of Comirnaty (COVID-19 Vaccine, mRNA) in individuals 16 years of age and older.

10/26/2021 — Vaccines and Related Biological Products Advisory Committee Meeting
The committee will discuss a request to amend Pfizer-BioNTech’s Emergency Use Authorization (EUA) for administration of their COVID-19 mRNA vaccine to children 5 through 11 years of age.

10/14/2021 – Vaccines and Related Biological Products Advisory Committee Meeting
The committee will discuss the Emergency Use Authorization (EUA) of the ModernaTX Inc. COVID-19 vaccine and the Janssen Biotech Inc. COVID-19 vaccine for the administration of an additional dose, or “booster” dose, following completion of the primary series, to individuals 18 years of age and older.

November 2, 2021 – CDC Recommends Pediatric COVID-19 Vaccine for Children 5 to 11 Years

Today, CDC Director Rochelle P. Walensky, M.D., M.P.H., endorsed the CDC Advisory Committee on Immunization Practices’ (ACIP) recommendation that children 5 to 11 years old be vaccinated against COVID-19 with the Pfizer-BioNTech pediatric vaccine. CDC now expands vaccine recommendations to about 28 million children in the United States in this age group and allows providers to begin vaccinating them as soon as possible.

YEAR 2022

Jun 17, 2022 FDA authorizes COVID-19 vaccines for children age 6 months and older

The Food and Drug Administration today authorized Moderna’s COVID-19 vaccine for children aged 6 months through 17 years old and Pfizer’s COVID-19 vaccine for children aged 6 months through 4 years old, as recommended this week by its vaccine advisory committee. The vaccines previously were authorized for older children.

Before vaccinations can begin, the Centers for Disease Control and Prevention must recommend the vaccines for these age groups. CDC’s Advisory Committee on Immunization Practices is scheduled to vote tomorrow on whether to authorize the vaccines for children age 5 and under.

December 08, 2022 Today, the U.S. Food and Drug Administration amended the emergency use authorizations (EUAs) of the updated (bivalent) Moderna and Pfizer-BioNTech COVID-19 vaccines to include use in children down to 6 months of age.

Children 6 months through 5 years of age who received the original (monovalent) Moderna COVID-19 Vaccine are now eligible to receive a single booster of the updated (bivalent) Moderna COVID-19 Vaccine two months after completing a primary series with the monovalent Moderna COVID-19 Vaccine.

Dec 9, 2022 CDC Expands Updated COVID-19 Vaccines to Include Children Ages 6 Months …

Following FDA action, today CDC expanded the use of updated (bivalent) COVID-19 vaccines for children ages 6 months through 5 years.

May 19, 2022 – CDC Strengthens Recommendations and Expands Eligibility for COVID-19 Booster Shots

Following today’s meeting of the Advisory Committee on Immunization Practices’ (ACIP), CDC is expanding eligibility of COVID-19 vaccine booster doses to everyone 5 years of age and older. CDC now recommends that children ages 5 through 11 years should receive a booster shot 5 months after their initial Pfizer-BioNTech vaccination series.

GC/wm

Why I’m Glad I Watched the Ken Burns PBS Propaganda Special Blaming the Holocaust on America’s Evil Trump Supporters (Or Their Terrible Nativist Parents and Grandparents)

TL;DR – Watch this sucker while ignoring the myopic neo-Bolshevik “refugee” propaganda, but instead keeping in mind the current COVID/WEF insanity, to get a grip on the incipient climate-excused holocaust of the depopulationists, which is the fault of SOCIALISM, same as the soon-to-be-dwarfed “Holocaust” of the 1930s and 1940s.

OK – just a bit more detail…..

Don’t watch the Ken Burns Holocaust special for any of the slanted, leftist, socialist messaging stapled onto the historical facts in a DNC-approved and ADL-edited way.

Watch this PBS special while subversively keeping in mind the new socialist, depopulationist, eco-nuttery holocaust which now exceeds 6 million COVID dead and will soon DWARF the old “Holocaust” of so much hypocritical and self-centered angst.

Calmly stroke Suspicious Cat, as the Holocaust is falsely linked to rejection of current “asylum seekers” in a face-palmingly stereotypical and Trump-hating way.

Watch this PBS special while “rebelliously” remembering that RIGHT NOW we are in a DESIGNED CRASH of the world economy, which will kill BILLIONS of innocent people if not stopped – and which is largely driven with the eager participation of globalist and socialist “Jazis” – who are no less evil than the Nazis of old – self-righteous in their “ESG/DEI” zeal, with their vain self-assurance that they and they alone know the answers which must be forced upon the world.

Watch this special remembering Andrew Cuomo, Anthony Fauci, Ralph Baric, Joe Biden, WEF, Klaus Schwab, Pfizer, CCP and Albert Bourla, and keeping close in mind, the NEW holocaust which has already killed over 6 million worldwide by the virus ALONE, and is already creating even-more-massive excesses in mortality in every country, in unacknowledged proportion to acceptance of the “vaccines”.

Watch this PBS propaganda special while remembering how the US and China co-created biological “gain of function” which literally DWARFS the mere chemical nastiness of a bug spray, “Zyklon B”, itself more comparable to Fauci’s murderous remdesivir, or the midazolam they apparently used for “COVID euthanasia” in the UK.

Watch this special while remembering the millions who died around the world from both virus and vaccines, including tens of thousands of Israelis, as secular Jewish leaders condemned their own and didn’t lift a finger, other than to censor Zev Zelenko, and to suppress their own report on the dangers of the vaccines they INVESTED IN.

Watch this special in strict analogy of the THEN unbelievability of the “final solution”, to the NOW unbelievability of “depopulation”.

Realize that the problem isn’t antisemitism or “refugee acceptance” – it’s SOCIALISM.

SOCIALISM KILLS – no matter which brand.

Representative Alexandria Ocasio-Cortez (D-NY) and Senator Ed Markey (D-MA) were joined by Democratic lawmakers from both the House and Senate on February 7, 2019, to introduce Green New Deal legislation.

Oh, hell. I said enough already. Do I really need to explain this?

If so, I’ll do it in the comments.

But the bottom line is that this special has a lot of great facts, which – if you are prepared to see them in the context of current events – are quite convincing that we ARE in the late beginning of yet another socialist holocaust.

Buckle up.

W

PS – Oh yeah – the URL…..

https://www.pbs.org/kenburns/us-and-the-holocaust/

PPS – The Depopulation Series – a Bibliography

The Population Control Shot – Introduction

The Population Control Shot – New Sodompox Limited Edition

The Population Control Shot – Did Bill Gates Gaffe, Troll, Let it Slip, Or None of the Above?

The Population Control Shot – CDC Backs Out of the Shot-Up Saloon Like Nothing Happened

The Population Control Shot – Understanding the Peoples Climate Temple

Conspiracy to Suppress Competing Science – The Case Against Bill & Melinda Gates

I think it is now quite clear that Bill and Melinda Gates need to get the hell out of science and medicine for the good of humanity.

I am going to show you why.

I am not saying that Bill Gates is doing anything new. I am saying that he moved his disastrous “Windows Effect” from information technology – which Gates corrupted and hindered with his inferior product and short-sighted greed – to human health – where Gates is doing the exact same thing, only with more obvious damage to society and individuals.

I’m going to start at the END – with the most recent bit of evidence, which finally compelled me to write this article.

Hat tip apudlo on Gab for reposting this link, leading me to this study.

https://gab.com/vaccineregrets/posts/107907074039803194

New Ivermectin Study — Same 70% Reduction in Deaths

Not using Ivermectin killed about 688,000 Americans

Igor Chudov

LINK: https://igorchudov.substack.com/p/new-ivermectin-study-same-70-reduction?s=r

This isn’t just a 70% reduction in mortality of COVID-19 relative to no treatment. This is 70% reduction relative to treatment with Anthony Fauci’s “gold standard of care”, remdesivir.

Actually – let’s take a bit of a sidebar and then a hypostrophe (return from a parenthetical discussion) on the subject of remdesivir.

Now – as I have said before, and I mean said before repeatedly, and again and again, remdesivir AT BEST does nothing…..

LINK: https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2781959

ARCHIVE: https://archive.ph/FrP5h

…..but more likely, it’s worse, and remdesivir is killing advanced hospitalized COVID-19 cases by mimicking the damage from advanced COVID-19 itself.

The Murder of Veronica Wolski by Fauci and Gilead’s Zyklon D

There will be justice for Veronica Wolski, because we will DEMAND IT. And until there IS justice, we will drag the CRIMES of Anthony Fauci and Gilead “Pharmaceuticals” and their SLEAZY ASSOCIATES thorough the headlines, over and over, until people SPIT IN THEIR PATH as they walk down the streets. So where do we begin? …

NIH and Gilead Blamecasting Remdesivir Renal Toxicity to an Excipient

Well, they can lock us out of The Q Tree, but they can’t stop the truth from getting out. Enjoy a post first over on The U Tree and now HERE. Here is a quickie in my WAR ON REMDESIVIR. Fellow Treeper barkerjim dropped an interesting document today, from back in July, which showed the …

Hat tip DP…. wait for the remdesivir part…..

Cardiologists encouraging q6 month V-compliance despite myocardial damage and the use of inpatient R-vir despite WHO recommendation against and overt kidney/liver damage contributing to death are manifestations of mass formation psychosis @PaLegis @dougmastriano @PAHouseGOP pic.twitter.com/7iKoA7IEJB
— Peter A. McCullough, MD, MPH® (@P_McCulloughMD) March 6, 2022

This is actually quite analogous to what the “medical establishment” did with mercury back in the day, when calomel and other mercury medicines killed and injured MILLIONS of Americans in the 19th century.

DEAR KAG: 20220304 – The Pub is OPEN / Mercury and Arsenic as the mRNA and Remdesivir of Pre-Fauci America

The Pub is OPEN! We are NOT serving mercurials or arsenicals today – or EVER – but we ARE serving MODERN SUBSTITUTES like penicillin – to the non-allergic, of course. While our beloved REAL bartender takes a needed break of unknown duration, we continue to ENDEAVOR TO PERSEVERE. Christmas Spirit And now, the rules of …

But let’s return to BILL GATES.

Fauci and remdesivir are another story. Bill Gates is all about the vaccines. If Gates is kicking remdesivir under the table, I would not be surprised, but I tend to doubt it, because Gates seems to respect OTHER corrupt players, to some extent.

The point is, this brand new study CONFIRMS what we know from many other studies – that ivermectin really does reduce death from COVID-19 – and that it does so substantially.

Not only THAT, but the “70% reduction” figure has appeared MULTIPLE TIMES before, and is not only confirming in its magnitude, but is also extremely indicting of Bill Gates, as we shall see in a moment.

One “70%” case is cited in the link – a recent Malaysian study – where is appears that the authors deliberately misinterpreted their data, effectively HIDING a 70% reduction in mortality by ivermectin, by claiming the “p” value of the results meant they were insignificant, being only 91% instead of 95% or 99% (basically, the study was too small).

This “capture and kill by underpowering the study” is a NIFTY TRICK, which was also discussed by Steve Kirsch, and which I have covered previously.

DEAR KAG: 20220225 – … Failure of Socialized Science and Peer Review Exposed in a JAMA-Published Ivermectin Study

The big picture, however, is that (1) authors have a variety of means of making a paper produce conclusions that are completely at odds with the data, and (2) they are using such techniques to satisfy their sponsors when the “science” doesn’t give the results hoped for by the sponsors.

Don’t believe me?

It turns out there is ANOTHER 70% reduction ivermectin paper we need to talk about.

And in that case, there is strong evidence that BILL GATES is behind the effective SCIENTIFIC BURYING of the result.

Hat tip to eilert and Sundance for this one.

This is the biggie. This is where Bill Gates showed his true self to the planet.

TIME and PERSISTENCE have narrowed down WHERE and WHEN it was, that ivermectin was blocked from becoming a universal treatment for COVID-19.

This work is mostly due to Tess Lawrie, who was one of the speakers (from England, via internet video) at the Defeat the Mandates rally in Washington, DC.

Sundance at CTH brings us the story HERE.

LINK: https://theconservativetreehouse.com/blog/2022/03/04/dr-andrew-hill-the-man-who-killed-millions/

The article frames a video by Tess Lawrie, which, as Sundance rightly states, is STUNNING. Yes, it is somewhat professionally produced, but speaking as a scientist, this is one of the most insightful and direct explorations of institutional scientific misconduct which has ever been put on the table.

LINK: https://rumble.com/vwg569-a-letter-to-andrew-hill-dr-tess-lawrie-ivermectin-suppression-killed-millio.html

It is shockingly clear from this video that ivermectin was saving OVER 70% – in fact 75% – of hospitalized patients who would have otherwise died. They are talking about tens of thousands of patients DAILY. Using an EXTREMELY safe drug.

This video lays it all out – who was responsible for the corruption of the conclusions of the preprint which blocked ivermectin – a FRONT ORGANIZATION for Bill & Melinda Gates called Unitaid. We don’t know the names of the individuals in Unitaid yet, but it’s very clear that TENS OF THOUSANDS immediately, and ultimately HUNDREDS OF THOUSANDS – worldwide even MILLIONS of people died – because of an ABUSE OF SCIENCE.

It’s very simple. Anybody can see what they did there.

“Let them die – we want the money.”

But now, let me tell you something MORE.

There is also evidence that Bill Gates has done EVEN MORE to block “old” drugs for COVID-19.

Begin with “LancetGate” and the “LancetGate Effect“. LancetGate was the first instance, where a FALSE anti-hydroxychloroquine paper – later RETRACTED – literally caused DEATHS that could be seen on a graph, due to panicked withdrawal of HCQ from patients in Switzerland, by a RASH bureaucratic ban on treatment with it.

This is explained in an article I did, covering a SECOND case of the LancetGate effect, where a ban on ivermectin was lifted, resulting in suppression of a wave of the delta variant in Indonesia.

LancetGate Effect 2.0 – Indonesia

The murderous LancetGate Effect is back, and this time it killed thousands before bureaucrats relented and allowed doctors to save patients. [ Hat Tip to barkerjim for alerting me to this Indonesian case. ] Part 1 – LancetGate Effect 1.0 and 1.1 Ah, the memories of LancetGate! That moment when “they” “finally” “proved” that hydroxychloroquine …

I have always suspected that Bill Gates was somehow behind the retracted LancetGate paper, but I’ve never been able to prove it. Part of that suspicion dated back to the very beginning of the COVID pandemic. When Bill Gates, “Mr. Vaxx and Vaxx Alone”, decided that treatments needed study, I knew that THE FIX WAS IN.

FIRESTARTER Bill Gates Downplays Effectiveness of Water on Fire – Says “We Need To Study All Kinds of Liquids and Promote The Best Ones”

Yeah. This fucker can PAY FOR MY RESPIRATOR. Just read this. The guy who funded the UNETHICAL virus research that gave me the fucking shortness of breath….. The guy who promoted a curiously fortuitous corona virus “exer-psy-op” while his CHINESE FRIENDS let loose the ChiCom-19 virus….. The guy who worked with DEMOCRATS to try to …

And then, when LancetGate hit, I suspected Gates.

However, it was only LATER that I stumbled upon ANOTHER instance of Gates’ apparent meddling in the scientific examination of hydroxychloroquine. Discussed HERE:

DEAR KAG: 20211224 – Christmas Eve – The Pub is OPEN / How Bill Gates Took Down Hydroxychloroquine

The Pub is OPEN again! With a blend of humor and seriousness, like any good bar, we celebrate this grand re-opening of WOLF’S PUB on Christmas Eve, December 24, 2021, by actually opening near closing time on Christmas Eve Eve, but what the heck. IT’S ALMOST CHRISTMAS. While our beloved bartender takes a needed break …

This one was actually a bit of a gold mine. Not only did I find that Facebook, Twitter, Gates and Pfizer were all tied behind a study which trashed hydroxychloroquine – there was ANOTHER study in the mix, funded by this gang, which pooh-poohed ivermectin.

These papers did NOT get big play in public – rather, they were used to quietly influence doctors behind the scenes. Gates is CUNNING, and he clearly does NOT want the “crowd” interfering in his delicate, moneyed, subversive operations.

He LEARNED after LancetGate, IMO, to be a bit more stealthy.

I have NOT looked at these two papers since the discovery of the funding. I do believe that when it first came out, I may have read the HCQ paper, if it’s the one I think it is, which was done in Brazil. I remember that at the time, I thought it was problematic for some reason, but I don’t really want to look at it again, because I think it would be better if OTHER scientists looked at these two studies and figured out what’s wrong with them.

Because I will BET MONEY there is something wrong with them. But I would rather just be the one to point out the funding issues, and let others find the science problems independently.

Now – there is one other potential scandal here, which almost nobody is talking about except me, and that has to do with the “suppression” of the fact that simple, normal, drug-store antihistamines have a rather profound effect in preventing death by COVID-19.

You didn’t know that, did you?

The Spanish nursing home study. Never heard of it, unless you follow a few sites like this one, or Jo Nova, or Karl Denninger.

This signal showed up in the literature several times, and NOBODY followed up on it. But in terms of saving lives, simple, over-the-counter antihistamines have been IMPRESSIVE.

All covered here:

The Zyrtec Rebellion

Everybody underestimates Spain. The last letter in “PIGS” is far less of an insult than an error. Years ago, when I was at a conference, and Japanese industrial spies were getting me drunk (it was a great red wine), I decided that I had to give them SOMETHING for their time and effort, if only …

AND HERE……

Dear KMAG: 20220103 Joe Biden Didn’t Win ❀ Open Topic / Benadryl Could Have Saved Grandma / The Gatesification of Science

Joe Biden didn’t win. This is our Real President: AND our wonderful REALFLOTUS. Hopefully, this great couple is getting some REST, because they may NEED IT. I am telling y’all – the Trumps may very well be on their way back to the White House in 1-3 years. In fact, the way Obammunism has been …

You see, it’s actually rather ironic, but while we were all distracted by the drama of hydroxychloroquine and ivermectin, nicely seeded by the other side, nobody paid any attention to the massive live-saving signal from drugstore antihistamines.

Something out in the public, that nobody could have stopped us from using. Something that – from THEIR point of view – could not have been allowed to become a public controversy, if they wanted the vaccines approved.

This is why – even though I am totally in favor of HCQ and ivermectin – I think it’s important to look deeper, and see how ALL OF US were fooled. The Spanish nursing home study was DONE treating patients in June of 2020. The results were in. The doctors finished their paper in September, but had already gone to the media 3 weeks into June.

There is no reason we could not have been saving people worldwide with their protocol, other than the likelihood that somebody didn’t want that knowledge to get out. And one of the ways to do that, is to set up a Hegelian conflict where the media sides AGAINST treatments in favor of the vaccines as “the only way”.

EVERYTHING after that is just a story of the FAILURE of human science, with all its “big data” and all its “artificial intelligence”, to FIND THAT SIGNAL, AMPLIFY IT, and START SAVING LIVES.

But that’s not what happened. Using a Hegelian process, we were made to fight over TWO DRUGS that THEY COULD CONTROL – and our minds were steered away from even safer and possibly even more effective common drugs that THEY COULD NOT CONTROL.

Even famotidine (a digestive tract H2 antihistaminic) is a distraction from the obvious truth that respiratory-tract-affecting H1 antihistaminics were found by both the Spanish authors and Dr. Chetty in South Africa to completely eliminate mortality from the inflammatory stage of COVID-19, if administered as soon as hypoxia ensues, or better still, at the first symptoms of the disease.

Well, here’s what I think.

I don’t think this signal was “lost”. I think this signal was covered up when possible, and distracted from when it could not be covered up.

And if you don’t think Bill Gates was somehow involved in that, you have a lot of catching up to do.

EVENT 201 SPONSORS:

Event 201 was designed to give people PRECONCEPTIONS.

Event 201 was designed to make sure people believed certain things – many of which science was about to find were simply UNTRUE. It was also designed to make sure people did NOT believe other things – or think them possible. And, I believe, Event 201 is also why much of the World Health Organization’s early advice was just plain BAD.

THEY were misled TOO.

At this point, I’m not sure how much Bill Gates is responsible for, but I do know this.

I am prepared to question every single word that comes out of his mouth.

He is NOT HERE TO HELP. I am not sure what in the hell he is up to, but he’s not here to help.

W

DEAR KAG: 20220225 – The Pub is OPEN / COVID-19 Vaccine Interference With AIDS and Syphilis Tests / Moscow Mule Revisited / Failure of Socialized Science and Peer Review Exposed in a JAMA-Published Ivermectin Study

The Pub is OPEN!

And we’re finally serving a NORMAL DRINK tonight. Even though it’s a SECOND ROUND.

STAY TUNED…..

While our beloved REAL bartender takes a needed break of unknown duration, we continue to ENDEAVOR TO PERSEVERE.

and what time of year is it now???

Christmas Spirit

We continue our WAAAAAY too-long celebration of Christmas by noting that some of our neighbors STILL have their lights and decorations up.

We saw a nice red Christmas bow laying in somebody’s yard by their driveway.

We ourselves just got rid of our tree.

And TODAY is the 25th of the month. That’s VERY “Christmassy”.

So yeah. Given that there are a few ~~days~~ ~~weeks~~ months AFTER Christmas where it’s STILL Christmas, that means we have a few more weeks left. Riiiiiiight?

Sure! So have some hot CHRISTMAS chocolate!

And now, the rules of the pub.

HOUSE RULES

God bless us, every one! Tiny Tim had such a beautiful soul. He hadn’t a mean bone in his body…unlike most of us. But in keeping with Christmas, we promise to honor Wolf’s rules and keep Scrooge at bay. The Utree is where the Ghost of Christmas Present will conduct you should you need to rattle some chains. Another option, should all hell break loose is here.

Now, back to business.

AMEN!

Free the January Brothers!

Current Art On The Wall

We’re just gonna segue into the next item with our selection, if that’s OK.

This gets a bit “planetary”…..

**Christiaan Huygens, Saturn, and Something**

https://owlcation.com/stem/Huygens-Mission-on-Titan

**LINK: https://www.instagram.com/p/BAOVsasAXhl/**

**Mercury**, the old cure for ***grandgore***.

COVID-19 Vaccine Interference With AIDS and Syphilis Tests

Earlier this week, RAC brought a news item from CTH, which really got me thinking:

FDA Warns of Vaccine Induced Positive Syphilis Test

This had to do with a CDC alert…..

LINK: https://www.cdc.gov/std/FDA-alert-12-20-2021.pdf

…..which was based off of an FDA alert (sketchy link)…..

…..which actually links back to a different CDC alert (even sketchier link)…..

WHATEVER.

Here is that final CDC alert. Only the top 3 paragraphs are important here.

Let me quote the text of those first 3 paragraphs for Zoe. I will make BOLD what is important.

Dear Partners in Prevention,

December 20, 2021

I’m writing to share the U.S. Food and Drug Administration (FDA) alert sent to clinical laboratory staff and health care providers about a syphilis test. The alert reports that false reactivity, or “false-positive,” Rapid Plasma Reagin (RPR; non-treponemal) test results, when using the Bio-Rad Laboratories BioPlex 2200 Syphilis Total & RPR kit, can occur in some people who received a COVID-19 vaccine and includes recommendations for addressing these potential false positives.

Historically, false-reactive RPR test results have been observed in people with systemic infections unrelated to syphilis, such as tuberculosis, rickettsial diseases, and endocarditis. False-reactive RPR testing also has been previously observed following immunization (specifically following smallpox vaccine). False reactivity with RPR can also occur during pregnancy.

Per CDC’s 2021 STI Treatment Guidelines, reactive RPR results should always be confirmed with treponemal testing (e.g., Treponema pallidum particle agglutination, TP-PA). This is, in part, because of the above-mentioned issue: false-positive nontreponemal test results can be associated with multiple medical conditions and factors unrelated to syphilis. According to FDA’s alert, treponemal testing for syphilis does not appear to be impacted by this issue.

Allow me to translate.

It turns out that “being vaccinated for COVID-19” throws off an ANTIBODY-BASED SYPHILIS TEST, and can give false positives.

The reason is that these are a sort of antibodies against substances released from cells attacked by certain diseases and conditions. Thus, they’re not exclusively the downstream product of syphilis.

Normally, certain diseases, certain vaccines, and pregnancy can all throw off this more rapid but less conclusive syphilis test, and that is part of the reason why people are supposed to follow up this easier test, with a test that looks for the actual organism which causes syphilis.

Thus, we have added one more cause for the test to be thrown off.

This is not the same as the HIV test that was thrown off by a particular Australian vaccine, because the antigen in the vaccine actually contained an HIV protein (gp41) as part of the vaccine, and created antibodies against HIV. I talked about that last week. That was a much more direct test interference, easily expected.

Saved From The Frankenvax

How a Psycho Vaccine Marrying the Infamous COVID Spike Protein to HIV’s Neurotoxic gp41 Was [Allegedly] Canned by a Mere Testing SNAFU How Australia Dodged The First Mad Vax Bullet of the WEF Scamdemic / Plannedemic Darwin Award Vaccine Featured Insane Merger of HIV and COVID But Failed Due to Buggering of AIDS Tests, NOT …

What I find interesting is that one of the things that normally sets off the syphilis test is endocarditis.

Endocarditis, which is inflammation of the inner surfaces of the heart, is one of the three main heart inflammations, thus being pretty damned close to myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the outer sac), both of which have very prominent correlations to the jabs.

So while this means that – NO – the shots are not giving people syphilis – the shots ARE basically acting like an illness, and very much like a known cardiac illness.

You were warned.

Now – while I was researching syphilis, I became interested in the treatment with compounds of mercury.

Traditional mercury-based pastes were used in cures. Whilst this was partially effective, the toxic side effects of the mercury probably outweighed any advantages.

This is actually a HUGE understatement.

It turned out that arsenic was considerably better.

The first effective treatment for syphilis was arsphenamine, discovered by Sahachiro Hata in 1909, during a survey of hundreds of newly synthesized organic arsenical compounds led by Paul Ehrlich. It was manufactured and marketed from 1910 under the trade name Salvarsan by Hoechst AG.^[88] This organoarsenic compound was the first modern chemotherapeutic agent.

It wasn’t too long after that success, that penicillin took over as the real cure for syphilis.

I will come back to MERCURY in a future post, because I found something quite amazing in its history.

But if you look ONE COLUMN TO THE LEFT and TWO ROWS UP…..

COPPER is also bacteriostatic and algicidal – and at concentrations below where it is a health risk. And THAT leads back to a DRINK that Grandmaintexas introduced us to……

Moscow Mule Revisited

Based upon my reading of Grandma’s post on the subject, the Moscow Mule simply is not a proper Moscow Mule unless it is served in copper vessels.

The health effects of COPPER are about as debatable as the effects of mercury – although, in general, copper is much less toxic, so when it’s being “not good for you”, it’s a lot less “not good for you” than lead. At the same time, copper is much MORE toxic to things like algae, fungi, plant roots, and other “pests”, than it is to us, and that is why it is found among the gardening pesticides in hardware stores. The antimicrobial activity of copper is extremely well-documented, but appears to be complex. Simply having copper in the household or workplace environment seems to have health benefits – and this was particularly noted back in the days of less sanitary environments. Water passing through copper fixtures tended not to spread disease.

We tend to forget about OLD SCIENCE, so we can’t put new things into good perspective.

LEAD and other CHEMICAL ADVANCES saved us from the horrible BIOLOGICAL diseases and maladies of the uncivilized life.

Did they have chemical consequences? Yes. The TRICK is REMEMBERING AND ADMITTING OLD RISKS AND BENEFITS while also DISCOVERING AND ADMITTING NEW RISKS AND BENEFITS, then BALANCING HONESTLY with the PROPER PRIORITIES which put PEOPLE FIRST.

It is VERY easy to see where CDC went off the rails with the COVID-19 vaccines, being unable to admit old benefits (of lasting immunity to caught and treated diseases), while also being unable to admit new risks (of vaccines using untested and immature technologies).

Likewise, looking back, it is easy to see that basic sanitation – not vaccination – REALLY conquered diseases. Vaccines came in, mopped up, and took all the credit, by design, because bad people realized that vaccines in the hands of a technological elite, combined with an ignorant populace they can essentially murder and experiment on at will, allow them to basically FARM HUMANITY.

Sorry, Bill Gates. We understand your social engineering of us. We know your M.O. We know your real intentions. Including for the “people of color” you pretend to care about.

You will note that, in general, the further down the periodic table one goes, the more toxic the metals. Surprisingly, the second-lightest one – beryllium – is quite toxic, but even lightweight aluminum simply isn’t all that bad, in the big picture (but you’ve got to keep it on the OUTSIDE). In contrast, if you get down and heavy there with mercury, thallium and lead, or even as far down the table as cadmium and indium, the metals can be quite toxic.

Lead used to be used for plumbing – enough to lend its name to the profession. Copper then took over – before plastic began to displace copper. Nevertheless, copper is still highly valued for plumbing, as well as for electrical wiring.

As noted above, copper in drinking water is an interesting beast. Lead and copper in drinking water are controlled by the EPA under something called the Lead and Copper Rule, or LCR. Note that the linked document, which talks about the most recent “upgrade” to the rule, is over 400 pages. Yeah – there is a MESS of goofiness outside the actual rule there. Most of the concern is about lead, which is now highly restricted. Here is all that is said about copper’s toxicity in the linked explainer:

Acute copper exposure causes gastrointestinal distress. Chronic exposure to copper is particularly a concern for people with Wilson’s disease because they are prone to copper accumulation in body tissue, which can lead to liver damage, neurological, and/or psychiatric symptoms. For a more detailed explanation of the health effects associated with copper see Appendix E of the final rule Economic Analysis (USEPA, 2020). EPA did not propose revisions to the copper requirements; thus, the final rule does not revise the copper requirements.

Copper is basically off the hook at 1.3 ppm or below. That number has not been upgraded. Why is that level important? In my opinion, it’s because copper is bacteriostatic and algicidal in practice at between 0.1 and 1.0 ppm. Thus, one can SAFELY DRINK water which is being purified against microorganisms with copper.

And THAT would include the Moscow Mule, depending upon how long it sits.

I refer you now to an excellent article, which relies on a breathless scaremongering headline, but actually DOES provide a balanced set of viewpoints on both the DANGERS and BENEFITS of dietary copper.

Sipping This Popular Cocktail Is a “Health Hazard,” Experts Say

AFTER 27 MINUTES, YOU MAY BE AT RISK OF HEAVY METAL POISONING.

LINK: https://bestlifeonline.com/moscow-mule-copper-news/

ARCHIVE: https://archive.fo/6YT3X

First of all, copper isn’t really a “heavy metal” IMO, but whatever. It’s heavier than some.

You will note, after reading at the link, that you have to drink a ton of Moscow Mules, or a few that have sat around for a very long time, to MAYBE get sickened by them.

In general, avoid drinking acidic things that have been in contact with copper for a long time, and you will be OK.

Remember – most household water has sat around in copper pipes for quite a while at neutral pH, and it’s simply not toxic (due to copper). You DO get less lead if you flush your water 30 seconds before getting drinking water, but again – we’re talking about levels that would make Romans, Victorians, and even people from 70 years ago howl with laughter at our prissy over-concern – even knowing the science.

Perspective is very important – as you are about to see in a beautiful example of the failure of modern science, thanks to CCP socialism infecting both global science and science publishing.

Failure of Socialized Science and Peer Review Exposed in a JAMA-Published Ivermectin Study

The fact that Pierre Kory now calls JAMA “PHAMA” is a nice short way of saying that medicine has been utterly taken over by the pharmaceutical industry, and IMO set back several thousand years. Hippocrates would be HORRIFIED by what has happened to medicine – and I say that as somebody OUTSIDE medicine, and a lot closer to the pharmaceutical industry.

IMO it’s too late to save the pharmaceutical industry from scandalous criminal survival – but it’s not too late to save the profession of medicine from utter moral death. And thus, you will be treated to my following scientific opinion.

Steve Kirsch doesn’t play defense. He saw how JAMA (the Journal of the American Medical Association) completely FUMBLED an ivermectin paper, and how Pierre Kory picked it up off the ground, taking complete control, but more or less just standing there, lamenting the bad refs and horrible cheating. So Kirsch did the only thing he does. He grabbed the ball from Kory and ran it back for a touchdown.

“New JAMA paper show Ivermectin blows the COVID vaccines out of the water”

This is an utter reversal of the conclusion of the paper.

All because some guy in the stands named “Massimaux” spotted the free ball and yelled “FUMBLE!!!”

If you understand science, and science publishing, then you will see that what Kirsch did here was BRUTAL. And I’m gonna show you where all the bruises and black eyes are.

I almost feel sorry for JAMA, but not enough to miss this opportunity to LEAP ONTO THE DOGPILE and give AMA’s hare-brained PC leadership a good WEDGIE.

Don’t worry about the AMA. They’re protected by Pfizer, Biden, and the media. And just like any good mafia arrangement, as long as AMA keeps saying the right things, and not saying the wrong things, everything is gonna be OK.

Everything but science. But that’s OK, too.

We’ll take care of things. Just like we did here.

Here is the Kirsch gab that grabbed my attention.

Repeating for Zoe, as well as our silicon friends…..

Steve Kirsch
@stkirsch
22h·

New JAMA paper show Ivermectin blows the COVID vaccines out of the water

https://stevekirsch.substack.com/p/new-jama-paper-show-ivermectin-blows?r=o7iqo&utm_campaign=post&utm_medium=web

New JAMA paper show Ivermectin blows the COVID vaccines out of the water

Whoops! How embarrassing! The CDC gave you bad advice. If you want to survive COVID, you should use the drug they said to avoid, and avoid the drug they said to…

stevekirsch.substack.com

View Link Feed

2,589 likes
208 comments
1,670 reposts
42 quotes

Now, as soon as I saw this, I was going….

“Wait a second. I thought there was some paper just out that Alex Berenson said was basically the end of ivermectin, although scientifically, I know that’s pretty much impossible. I know there is SOME explanation for why this paper (which I have not read yet) has to be deviating in some way from the MANY papers that show limited but solid efficacy – and especially against DEATH – just like HCQ. But this CANNOT be the same paper. No way! Kirsch would not be saying this unless the results were stunningly IN FAVOR of ivermectin, and there is no WAY that some authors with a NEGATIVE-LEANING study would be……. I mean….. WHAT THE HELL????”

SO – I just stopped to see what in the hell paper Kirsch was talking about.

YUP.

This is the SAME PAPER.

ARTICLE: https://jamanetwork.com/journals/jamainternalmedicine/fullarticle/2789362

SUPPLEMENTARY: https://cdn.jamanetwork.com/ama/content_public/journal/intemed/0/ioi220006supp2_prod_1644957301.65433.pdf

This is the SAME PAPER that caused Alex Berenson to issue TWO articles:

Ivermectin fails

To the ivermectin fanatics

Now we’ve discussed (in the comments on this site) Berenson’s very weird attack on Robert Malone when they appeared together on Fox News, which didn’t make sense THEN, but which does NOW – and I will explain that momentarily. But first, back to Kirsch.

Kirsch explains that – YES – this paper states in BOTH its abstract and its conclusion the following:

“The study findings do not support the use of ivermectin for patients with COVID-19.”

However, that is NOT what the data says.

Certainly not to everybody.

Certainly not to me.

In other words, DIFFERENT scientists (like Kirsch, Kory, me, and an anonymous Twitter poster names Massimaux, who found the key issue) have looked at the data, and see something quite different.

Kory goes into a rather long analysis of the whole war against ivermectin, but Kirsch digs into Kory’s article and then finds and elucidates the key nugget – discovered by Massimaux – that just ends the arguments.

It helps to read this in Kirsch’s article, but if you’re going to be lazy, I’ll explain here.

Here is Massimaux’s tweet:

In the I-TECH study, of 490 patients, 241 got Ivermectin and 331 were vaccinated.

Can we compute the vaccine effectiveness AGAINST DEATH and Ivermectin effectiveness AGAINST DEATH? Yes, we can! See the figure.

Which prevented more deaths, The Vaccine or Ivermectin? pic.twitter.com/WszQMQkAYX
— Massimaux (@masimaux) February 20, 2022

Look at the bottom line in the two tables and compare. Not only is ivermectin CLEARLY better than the vaccine at preventing death – the significance of the result is significantly greater.

If the efficacy of ivermectin against death is not true, then very little else in the study is true.

This data says that ivermectin is exactly what we’ve been saying it is. It’s not a miracle cure, but it WORKS – particularly in preventing DEATH – its only real purpose. That result is IN THE PAPER. It is IN THE DATA. And if the authors want to argue that it’s not in the data, because it’s not significant enough, then nothing ELSE is in the data, because most everything else is even LESS significant.

Now it’s very important to realize that this nice little pair of tables FROM THE DATA is not due to the original authors – it’s due to a POST-PUBLICATION “peer review” by somebody who looked at the very same data, and PROVED using the authors’ own data that they were WRONG to say that the data didn’t support use of ivermectin.

So why did the authors tack on that wrong statement?

Did the EDITORS make them tack on that statement?
Did the AUTHORS tack it on to get the paper to publish?
Or is the “peer bias” against ivermectin, mostly due to the media, SO STRONG that scientists didn’t even look through their own data to see a conclusion they didn’t want to see?

Or is it a combination of ALL of these?

It is clearly in the data that ivermectin is three times as effective as the vaccines in preventing death. Even more importantly, if you add in what is known OUTSIDE the paper in question – namely the adverse effects of the vaccine and the safety of ivermectin, then it’s a no-brainer to NOT take the vaccine and to just use ivermectin. And Kirsch explains THAT rather nicely.

The data LITERALLY justify our position.

This was my hunch all along, and as vaccine side effects loomed larger and larger, and ivermectin proved to be rather shockingly harmless, even at antiviral doses comparable to large-animal systemic antiparasitic doses. All ivermectin had to do was prevent death to some moderate extent, and it was a no-brainer that people should take it.

To conclude anything else, based on the data, is murderous folly, in my opinion.

When I was a young lad – a mere student – but also one who WROTE PAPERS (because I had a great professor who TRAINED US to be full-blooded scientists), we EXPECTED to be CRITICIZED in peer review by people exactly like Steve Kirsch, Pierre Kory, and myself. We expected that others would look at data and see it completely differently.

And we would then have to ACKNOWLEDGE the alternative interpretations, or convince the editors that the criticism was not even worth acknowledging (a VERY rare occurrence in any legitimately contested field).

My lab had PRACTICE criticizing other people’s work – and we expected it in return. I personally found quite a few errors in the literature. Most were small – mostly problems of the writing – but some were huge and affected the science. Sometimes the big errors would only partially alter the author’s conclusions, but other times they had a significant impact.

However, I have to admit that I never ran into data which PROVED THE OPPOSITE of the authors’ main conclusion – even if only to the critic – and THAT is what we have here.

PEER REVIEW is designed to subject a paper to (hopefully at least TWO) critical readers who will very likely DEMAND improvements. Those improvements often mean acknowledging DIFFERENT views of the data as being possible and maybe even reasonable.

That kind of QUALITY peer review was VERY OBVIOUSLY not done here.

What we have RIGHT HERE is a demonstration that HERD REVIEW is much more important than PEER REVIEW.

PEER REVIEW is subject to BIAS. It is subject to SUBVERSION and GAMING.

I go back to the Zhang mask paper, for crying out loud.

To me, this will always remain a horrifying example of “fitting the data to the theory”, rather than looking to see what the data says. You can just look at this graph and see the crime.

I lay this stuff SQUARELY at the feet of SOCIALISM, which has politicized science and removed control of science from the people of science themselves, investing much of it in a media which WILL NOT question government narratives. People raised under socialism who become “go-alongers” – and so SOME degree that is everybody – stop questioning things that need to be questioned.

I have WATCHED and I have SEEN how WEF and CCP corruption have degraded science everywhere.

They’re not going to fix this stuff – at least not yet.

But until then, know this:

Ivermectin WORKS, and it was just proven by people who said it doesn’t work.

Thanks to HERD REVIEW.

One last point.

Why did Alex Berenson not see this?

IMO, it’s because Berenson is simply not a scientist – he’s an investigative journalist. Thus, his virtue-signaling attack on Malone was meant to show “journalistic balance”, NOT that he himself had deeply researched the history of the topic, in which case he (Berenson) would have likely said “Yes, Malone really is the most foundational of the founding fathers of the tech.”

But let’s not blame Alex too hard. THE AUTHORS OF THIS STUDY – that’s right – the authors themselves – didn’t see it, either.

See what I’ve always said? Real science is contentious.

But it has a good heart.

It wants the TRUTH.

ENJOY THE SHOW.

Thank you all for being here. Have a great weekend.

W

Who Approved and Upheld These Vaccines? The Covid Second Opinion Forum Held by Ron Johnson vs. the FDA Vaccines & Related Biological Products Advisory Committee (VRBPAC)

A background research post by Gail Combs

PREFACE

by Wolf Moon

It is useful for me to explain Gail’s post – to help you understand the importance of it.

People in government regulation of science and medicine do not make decisions in a vacuum – but they may make their decisions in an artificial atmosphere which is created, composed, and altered by those with the extreme power and ability to CONTROL INFORMATION.

LancetGate was very demonstrative of this ability to control science and medicine.

After watching a variety of FDA decisions under the Trump and Biden administrations, it has become very clear to me that FDA resides in a political and economic crosswinds, highly influenced by many parties with strong expectations and abilities to influence. And yet, the shocking (but welcome) advisory recommendation AGAINST COVID vaccine boosters – then overridden by the political operative Rochelle ~~Alinsky~~ Walensky in CDC – shows how a coordinated injection of honest medicine and common sense into FDA decision-making (THANK YOU, Steve Kirsch!) can sometimes make its case heard – even if only momentarily.

Sadly, it seems to me that Pfizer is back in the driver’s seat again. We thus have to ask WHY.

What Gail has done is to look at one endpoint of the argument (frontline doctors and publishing scientists who have run into the problems), which leads to the other, where we begin to find the reasons why FDA generally decides things in favor of big industry and big government, and not to the benefit of individual patients and doctors.

By looking at the doctors and scientists who supported logical and ethical TREATMENT of COVID-19, and who were wrongly and unethically BLOCKED and DENIED PERMISSION at every point – we can see that undue industry and political influence in NIH, CDC, and FDA are most likely responsible for decisions that make absolutely no sense to truly independent scientists and doctors. The video Gail includes is rather astounding in terms of showing us how much went wrong. What we are now seeing reminds me of science and medicine in the Soviet Union. Absolutely incredible.

What Gail has done here is to “follow the influence” – to show that FDA decision-making has NOT been in a vacuum, precisely because the members of the FDA advisory committee are not truly independent, but are in fact actors for the very same powerful forces that benefit from FDA decisions which are now inscrutable at the doctor-patient frontline.

Perhaps even more astoundingly, the very SYSTEM of NIH, FDA, and CDC seems to be designed, at this point, to leave NOBODY ACCOUNTABLE. Advisory groups and even department responsibilities are created, rearranged, and dismissed, so that NOBODY takes responsibility for mandates that defy logic and even violate the common medical sense of the past.

If something goes wrong in this chaotic system of responsibilities in the wrong places, you either blame everybody or nobody at all. This is why, in my opinion, the entire federal governent had to get rid of Trump.

DIG ALONG WITH GAIL, as she finds the CLUES – first in the testimony of Ron Johnson’s witnesses – then in the backgrounds of members of an important FDA advisory panel.

With that, here’s Gail.

The Covid Second Opinion Forum

It would be nice to let Senator Johnson know we saw this:

CONTACT: https://www.ronjohnson.senate.gov/contact

Offices – Mail address and Phone: https://www.ronjohnson.senate.gov/office_locations

MANY THANKS TO GA/FL and Wolf M00n for alerting us to the Covid 2nd opinion Forum

Here’s a must watch – A SECOND OPINION – SENATOR RON JOHNSON FORUM.
Begins at 40:19 – https://rumble.com/vt62y6-covid-19-a-second-opinion.html
“Discussion begins around 40 minute mark. Sen. Ron Johnson moderates a panel discussion, COVID-19: A Second Opinion. A group of world renowned doctors and medical experts provide a different perspective on the global pandemic response, the current state of knowledge of early and hospital treatment, vaccine efficacy and safety, what went right, what went wrong, what should be done now, and what needs to be addressed long term.”
More at https://www.ronjohnson.senate.gov
GA/FL

It is five hours long and I went through the whole video. I recommend listening to it as you work on other things since there is not much to watch. It is much better than the speeches at the March Against Mandates.

My, comments posted 1/25/2020:
1:41:50 – 1:50:00 Dr Paul Marik on Remdesivir:
4 million hospitalized 850,000 million died. He says cheap approved drugs could have save 500,000 lives (That is the 1/2 million again that I figured out by a different method.)
He eviscerated NIH/FAUCI.

Fauci Told POTUS Remdesivir was good 10 days in. Researchers Changed the study END POINT to HIDE DEATHS. The OTHER study SHOWING the deaths/toxicity of Remdesivir in Ebola trial was released at 11:00 am JUST before the Afternoon presentation of the corrupted Remdesivir-Covid study that was presented by Fauci to POTUS. (More on this below) He also mentioned U.S. Centers for Medicare & Medicaid Services gives bonuses to hospital to treat MEDICARE (the old and ‘useless’) patients with this toxic drug.

Steve Kirsch made it clear he thought it was corruption and worse several times.

Incriminating evidence – Steve Kirsch’s newsletter
New VAERS analysis reveals hundreds of serious adverse Events that the CDC and EDA Never Told Us About

3:12:00 MyFreeDoctor (dot)com:
This group treated 150,000 and only lost four.

3:35:00 Dr Peter McCollough talks about vaccines:
Originally there were three different advisory boards during the trials but when it came to the EUA those boards were gotten rid of AND THAT IS WHY CLOT SHOT WAS NOT PULLED IN JANUARY 2021!
Steven Kirsch says right after that there is HARD evidence at least 4 in the CDC/FDA were getting royalties…

4:02:00
The risk increases with each shot. mRna was ENGINEERED to TAMP DOWN RESPONSE to evade ADE BUT it looks like it ALSO tamps down response to viruses, bacteria, and cancer.
New Study Dr Voss out of the Netherlands.
There are too many Dr Voss in the netherlands for me to hunt down the correct one.
https://pubmed.ncbi.nlm.nih.gov/?term=voss%20netherlands&sort=date
(Could be KL Koss since she has papers about the heart and colon and cancer. papers: https://pubmed.ncbi.nlm.nih.gov/?term=Koss+KL&cauthor_id=8943944

4:43:00 Attorney Tom Renz:

He has Dept of Defense Whistleblowers with the data from the D-Med data base. They have taken data ‘snapshots’ over time and it shows THE DATA BASE WAS TAMPERED WITH TO HIDE THE INJURIES TO OUR SOLDIERS!
Senator Johnson Ordered PRESERVE YOUR RECORDS….

January 25, 2022 14:52
Apparently Daniel Horowitz chased down Attorney after the Ron Johonson Senate Hearing for some additional clarifications.
https://thelibertydaily.com/bombshell-cover-up-cancer-diagnoses-in-the-military-rose-over-three-fold-since-jabs-were-introduced/
para59r

5:05:00
Myocarditis and heart Hits 18 to 24 yr old males the worst. up to 50 years 21,000 cases so far.
A lot more good info.

Dr. Christina Parks made comments through out the presentation.

January 25, 2022 20:09
Yes – Dr. Christina Parks has made some excellent points about how differently people with African genetic background react to CV19 AND THE VACCINES.
Ethnicity does matter in medicine – my sister had concurrent dengue fever and malaria and her response was severe and peculiar to a certain ethnicity so….we learned may have some middle eastern/african blood somewhere previously unknown to us.
GA/FL

The Timeline of FDA Decisions

Heading down the Rabbit Hole on Vaccines that Dr Peter McCollough opened.

Emergency Use Authorization — FDA
As background, this gives the laws, who has the authority and the timeline.

TIME LINE:

October 13, 1976 – New York Times:
Swine Flu Program Is Halted in 9 States As 3 Die After Shots
“After the deaths, swine flu vaccinations were halted throughout Allegheny County, which includes Pittsburgh, and the Federal Center for Disease Control sent doctors to investigate….“

September 1, 2020 CNN
Past vaccine disasters show why rushing a Covid-19 vaccine now would be ‘colossally stupid’
This is actually a very good article on BAD vaccines and what it can do to the public’s trust.

And then we come to the FDA, the meetings and WHO is on the board.

October 22, 2020
Discussing, in general, the development, authorization and/or licensure of vaccines to prevent COVID-19

On October 22, 2020, the Center for Biologics Evaluation and Research’s (CBER), Vaccines and Related Biological Products Advisory Committee (VRBPAC) will meet in open session, to discuss, in general, the development, authorization and/or licensure of vaccines to prevent COVID-19.
FDA

Those are probably the three boards Dr Peter McCollough talks about. The third was the FDA Vaccines and Related Biological Products Advisory Committee that hold these meetings. Note they are meeting just before the election and it contains ALL three boards.
….

These meetings are AFTER the STOLEN ELECTION but again all three advisory boards are present.

December 10, 2020
Discussing First Emergency Use Authorization Request for a COVID-19 Vaccine

On December 10, 2020, the Center for Biologics Evaluation and Research’s (CBER), Vaccines and Related Biological Products Advisory Committee (VRBPAC) will meet in open session to discuss Emergency Use Authorization (EUA) of the Pfizer-BioNTech COVID-19 Vaccine for the prevention of COVID-19 in individuals 16 years of age and older.
FDA

December 17,2020

Discussing Second Emergency Use Authorization Request for a COVID-19 Vaccine

Agenda
The meeting presentations will be heard, viewed, captioned, and recorded through an online teleconferencing platform. On December 17, 2020, the Center for Biologics Evaluation and Research’s (CBER), Vaccines and Related Biological Products Advisory Committee (VRBPAC) will meet in open session to discuss Emergency Use Authorization (EUA) of the Moderna, Inc., COVID-19 Vaccine for the prevention of COVID-19 in individuals 18 years and older.
FDA

December 15, 2020 updated December 18

The ACIP met last week to review the Pfizer-BioNTech vaccine and recommended moving forward with its distribution to anyone over age 16. The FDA issued an EUA on Saturday following the meeting and notified the CDC and Operation Warp Speed to coordinate distribution plans. Initial doses were shipped over the weekend. The first round of deliveries will be completed in all 50 states this week…
Pfizer’s initial distribution of vaccines will be given to 21 million health care workers and 3 million mostly elderly people living in long-term care facilities.
As vaccines are deployed, data on potential or delayed side effects will be collected to answer questions that would have been addressed in long-term trials with millions of participants under nonemergency circumstances….
Nat’l Conf. of State Legislators

December 14, 2020, 8:33 PM – Black nurse in New York, Sandra Lindsay, gets the first vaccine.

A month later we get the first Adverse Reaction Reports.
January 18, 2021 – Coronavirus: California calls for pause, investigation after Allergic Reactions to Moderna Vaccine

Biden is installed in the White House and the FDA/CDC does no real investigation. Instead NOTE THE CHANGE IN MEETING MINUTES.

February 26, 2021
Discussing Third Emergency Use Authorization Request for a COVID-19 Vaccine

Agenda
The meeting presentations will be heard, viewed, captioned, and recorded through an online teleconferencing platform. The committee will meet in open session to discuss EUA of the Janssen Biotech Inc. COVID-19 Vaccine for active immunization to prevent COVID-19 caused by SARS-CoV-2 in individuals 18 years and older. <== NO ADDITIONAL ADVISORY BOARDS!
Meeting Materials
FDA intends to make background material available to the public no later than 2 business days before the meeting. <== THIS IS THE INFORMATION people are having to SUE FOR!
FDA

Note there are NO MEETINGS TO DISCUSS DEATHS OR ADVERSE REACTIONS! This is the NEXT MEETING:

June 10, 2021

Discussing Pediatric Use of COVID-19 Vaccines

The Committee will meet in open session to discuss, in general, data needed to support authorization and/or licensure of COVID-19 vaccines for use in pediatric populations.
Meeting Materials
FDA intends to make background material available to the public no later than 2 business days before the meeting. If FDA is unable to post the background material on its website prior to the meeting….
FDA

Now we come to the meat, exactly who is at those meetings?

The VRBPAC Advisory Committee

The Committee reviews and evaluates data concerning the safety, effectiveness, and appropriate use of vaccines and related biological products which are intended for use in the prevention, treatment, or diagnosis of human diseases, and, as required, any other products for which the Food and Drug Administration has regulatory responsibility. The Committee also considers the quality and relevance of FDA’s research program which provides scientific support for the regulation of these products and makes appropriate recommendations to the Commissioner of Food and Drugs.
The Committee shall consist of a core of 15 voting members including the Chair. Members and the Chair are selected by the Commissioner or designee from among authorities knowledgeable in the fields of immunology, molecular biology, rDNA, virology; bacteriology, epidemiology or biostatistics, vaccine policy, vaccine safety science, federal immunization activities, vaccine development including translational and clinical evaluation programs, allergy, preventive medicine, infectious diseases, pediatrics, microbiology, and biochemistry.
FDA

Applying for Membership on FDA Advisory Committees

As part of the Food and Drug Administration’s (FDA’s) ongoing efforts to recruit qualified experts with minimal conflicts of interest who are interested in serving on FDA advisory committees, FDA is requesting nominations for members to serve on its advisory committees….
Conflicts of Interest:
Potential candidates are asked to provide detailed information concerning such matters as financial holdings, employment, and research grants and/or contracts in order to permit evaluation of possible sources of conflict of interest.
FDA

Oooh Boy, they do not sound good. I am digging up and placing here a lot of info on each individual. However I have screened out much much more. What struck me, is out of the sixteen only three do not have major expertise in pediatrics. ALL have ties to NIH/Fauxi or the FDA or the CDC. Some have ties to drug companies and more than one has ties to China. Most are women and three are foreign educated and probably not American born. Out of over 300 million people, you would think they could find Americans.

First a cameo of each of the players, and then if you wish you can look at some of the other information I dug out. If you click on the name it takes you to the information they provided to the FDA, often pages and pages citing the papers they wrote and who they worked for. This is the information I used with some added from other sources.

CAMEOS

DIRECTOR
Prabhakara Atreya, Female connected to Fauci She has no FDA bio.

Ph.D. biochemistry Memorial University of Newfoundland, in Canada 1987

Wayne State University, School of Medicine, Detroit, MI 1989 – 1990 (messing with fiber cell membranes of frog, chick, bovine, rabbit and human lenses)

Plant Pathology, University of Kentucky, Lexington KY – Papers 1990 &1995

FDA since 2010 per BIO but actually a paper shows she was working @ FDA in 1999.

NIH paper shows she was at NIH in 1998
Plant Pathology, University of Kentucky, Lexington KY – Papers 1990 &1995 (Only 13 papers found)

…..

Chair
Hana El Sahly, M.D.
Baylor College of Medicine (Woman)

Wrote paper on Remdesivir used by Fauci to trick President Trump. The one referred to by DR. McCullough

…..

Paula Annunziato, M.D. ***
Vice President and Therapeutic Area HeadVaccines Clinical ResearchMerck

Seems to specialize in Pediatric Vaccines.

Archana Chatterjee, M.D., Ph.D.
Dean Chicago Medical School (Woman)

specialises Pediatrics Vaccines

Pune University, Maharashtra, India 1979-1983

Army Medical Corps, Military Hospital, Gaya, India, 1985 -1988

She is nationally recognized for her work in vaccine development for human papilloma viruses – think Gardasil. I wonder how well acquainted she is with Gregg Sylvester, below & Bill Gates? – Controversial vaccine studies: Gates and Infertility

…….

CAPT Amanda Cohn, M.D.
Expertise: Pediatrics, Vaccines

Chief Medical Officer – National Center for Immunizations and Respiratory Diseases – CDC
The mission of the National Center for Immunization and Respiratory Diseases (NCIRD) is the prevention of disease, disability, and death through immunization

59 Scientific papers: many authored with Nancy E Messonnier

Time to check the Atlantia graveyards… And I am NOT kidding.

…..

Hayley Gans, M.D. (woman)
Expertise: Pediatrics, Infectious Diseases
Department of Pediatrics
Stanford University Medical Center

Author with a bunch of Chinese with FUNDING from China, using the bogus PCR test to say people who have recovered can catch Covid again and re-infect others. This is WHY natural immunity was never on the table and vaccines were.

….

Holly Janes, Ph.D.
Expertise: Biostatistics
Professor – Fred Hutchinson Cancer Research Center
Vaccine and Infectious Disease Division
Division of Public Health Sciences – Seattle, WA

Holly is a biostatistician working on the design and analysis of vaccine studies, with a particular expertise in HIV prevention and vaccine science. Worked for NIH and Bill & Melinda Gates Foundation.

…..

Michael Kurilla, M.D., Ph.D.
Expertise: Infectious Diseases, Pathology
Director, Division of Clinical Innovation National Center for Advancing Translation Sciences
National Institutes of Health (NIH <– He works for Fauci)
Bethesda, MD 20852

….

Myron Levine, M.D., D.T.P.H., F.A.A.P

Expertise: Infectious Diseases

Associate Dean for Global Health – Vaccinology and Infectious Diseases

Center for Vaccine Development – University of Maryland School of Medicine Baltimore, MD

Faculty at CVD have served in critical leadership roles in U.S. and international research and policy efforts. For example, Neuzil co-chaired the COVID-19 Prevention Trials Network, a research network established by the National Institute of Allergy and Infectious Diseases [ Dr. Fauci was appointed director of NIAID in 1984.] in response to the pandemic. Vaccine research at CVD continues, with an emphasis on reaching the populations most impacted by COVID-19 and testing pediatric vaccines.
University of Maryland

….

H. Cody Meissner, M.D. (Male)
Expertise: Infectious Diseases

Professor of Pediatrics – Tufts University School of Medicine
Director, Pediatric Infectious Disease

H. Cody Meissner, MD, is a leading national expert on childhood vaccinations who consults with the Centers for Disease Control and Prevention on periodic updates to the recommended immunization schedule for newborns through 18-year-olds. At Tufts Children’s Hospital at Tufts Medical Center he heads the Division of Pediatric Infectious Diseases…
H. Cody Meissner, MD, Vice Chair (’19)
H. Cody Meissner, MD | Tufts Medical Center

…..

Paul Offit, M.D.

Expertise: Infectious Diseases

Professor of Pediatrics, Division of Infectious Diseases, The Children’s Hospital of Philadelphia

Paul A. Offit, MD is the Director of the Vaccine Education Center at the Children’s Hospital of Philadelphia as well as the Maurice R. Hilleman Professor of Vaccinology and a Professor of Pediatrics at the Perelman School of Medicine at the University of Pennsylvania. He is a recipient of many awards including the J. Edmund Bradley Prize for Excellence in Pediatrics from the University of Maryland Medical School, the Young Investigator Award in Vaccine Development from the Infectious Disease Society of America, and a Research Career Development Award from the National Institutes of Health. Dr. Offit has published more than 160 papers in medical and scientific journals in the areas of rotavirus-specific immune responses and vaccine safety….
FDA

In 2017, Dr. Offit was a weekly columnist for The Daily Beast.

A look at his recent peer-reviewed papers shows he is targeting vaccine hesitant parents.

https://pubmed.ncbi.nlm.nih.gov/?term=Offit+PA&cauthor_id=24011750&size=20

This says it all:

Plotkin SA, Offit PA, Reiss D.: Important New Resource for Clinicians Giving Expert Witness Testimony on Vaccines. Pediatr Infect Dis J. 37(12), Dec. 2018.

To the Editors:

Vaccination is under attack by individuals who occasionally use the legal system to oppose mandatory vaccination laws and in some cases to obtain exemptions for particular children whose parents are opposed to vaccination. During the legal proceedings, as we have witnessed, experts testifying in favor of vaccination may be challenged with references from journals of doubtful quality that oppose vaccination.
To provide important references that discuss and disprove claims made against vaccines, the Vaccine Education Center at the Children’s Hospital of Philadelphia has created a library of references addressing certain safety issues that may be useful as an aid and refresher to clinicians giving expert testimony on the safety of vaccines and to lawyers defending vaccination of children.
The Children’s Hospital of Philadelphia legal library may be entered through the web address vaccine.chop.edu/safety-references.
We would be grateful if you could inform your colleagues about the availability of this resource, which should be of great value for experts testifying for vaccination and for clinicians who need to convince parents about vaccine safety. https://journals.lww.com/pidj/Fulltext/2018/12000/Important_New_Resource_for_Clinicians_Giving.42.aspx
The Pediatric Infectious Disease Journal

………..

Steven Pergam, M.D.
Expertise: Infectious Diseases
Medical Director
Infection Prevention
Seattle Cancer Care Alliance — Seattle, WA

He seems to specialize in cancer and immuno-compromised and seems to be the best of a bad bunch, until you see he is tied at the hip to NIH & CDC from 2009 to present as well as to various drug companies.

….

Jay Portnoy, M.D.

Expertise: Consumer Representative (This is the guy representing the public)

Professor of Pediatrics

Medical Director of Telemedicine Section of Allergy, Asthma and Immunology

Children’s Mercy Hospital Kansas City, MO

150 papers mainly on allergies. American College of Allergy, Asthma & Immunology – “…a professional medical association of more than 6,000 allergist-immunologists and allied health professionals…” AND if you search long enough…. You find the American College of Allergy, Asthma & Immunology wrote an Article urging allergists to support more funding for NIH (Fauci)

He is also on a Task Force Paper recommending those with severe egg allergies to go ahead and get the Flu vaccine, just do it at the allergist because “… personnel to recognize and equipment to treat anaphylaxis need to be immediately available…”

….

Andrea Shane, M.D., M.P.H., M.Sc.

Expertise: Pediatric & Infectious Diseases

Professor of Pediatrics, Director Division of Pediatric Infectious Diseases – Emory University School of Medicine – Atlanta, GA

International exchange fellowship, Children’s Hospital at Montefiore and Beijing Children’s Hospital, Beijing, China October-November, 1999

Lieutenant Commander, United States Public Health Service, 2001-2003;

Inactive Reserve Corps (IRC) 2003-until IRC dissolved in 2010.

Centers for Disease Control and Prevention, Advisory Committee on Immunization Practices (ACIP) respiratory syncytial virus (RSV) immunoprophylaxis working group, appointed member, 2009-until committee dissolved by CDC in 2011.

01 August 2007- 01 August 2016 Co- investigator, NIH/NIAID/DMID Vaccine and Treatment Evaluation Unit (VTEU)

influenza vaccine to breastfeeding women trial, DMID#09-007;

…..

Paul Spearman, M.D.
Expertise: Pediatric & Infectious Diseases

Director, Division of Infectious Diseases
Albert B. Sabin Chair in Pediatric Infectious Diseases
Cincinnati Children’s Hospital Medical Center
Professor, Department of Pediatrics
University of Cincinnati School of Medicine Cincinnati, OH

This guy is a really big heavy weight.

There is cross-over with the lady above, Andrea Shane. Any bets he pulled her in to be his ‘female puppet’ – a good little government soldier?

03/2009-09/2016: Vice Chair for Research Department of Pediatrics Emory University School of Medicine

03/2009-09/2016: Chief Research Officer Children’s Healthcare of Atlanta Atlanta, GA

[Andrea Shane is Attending Pediatrician Children’s Healthcare of Atlanta Emory Healthcare Grady Health 2006 – present ]

This guy has a full page of COMMITTEE MEMBERSHIPS, National and International, and a whole section for NIH Councils and Study Sections AND… NIH/NIAID HIV Vaccine Trials Network – Protocol Chair, HVTN 088 Protocol 2010-present

Not to mention his connections to the drug companies and China.

………

Geeta K. Swamy, M.D.
Expertise: Infectious Diseases
Senior Associate Dean Vice Chair for Research & Faculty Development
Associate Professor, ObGyn, Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine
Duke University, Durham, NC

2004 – 2006 Duke University Associate Faculty Department of Obstetrics & Gynecology Division of Maternal-Fetal Medicine & Division of Clinical & Epidemiological Research

2009 – present Duke University Vaccine Trials Unit Investigator Duke Translational Research Institute Durham, NC

Grants from, NIH-NIAID, GlaxoSmithKline, CDC-NCIRD, ACOG/Merck & Company,

2015

Consultative Workshop: Immunology Research Gaps Related to Maternal Immunization – Bill & Melinda Gates Foundation

WHO Brighton Collaboration Global Alignment of Immunization Safety Assessment in Pregnancy – Chair, Fetal Distress Working Group

…

Gregg Sylvester, M.D., M.P.H. +
Expertise: Alternate Industry Representative
Vice President – Medical Affairs, Seqirus Inc., Summit, NJ

• Launched Pfizer’s Pediatric and Adult Pneumococcal conjugate vaccine,

Spearheaded science-based rationale to preserve Pfizer’s Prevnar 13 infant schedule in US recommendations

• Launched Merck’s HPV4 vaccine in over 100 countries

• Partnered with community organizations in Delaware to reduce infant mortality, teen pregnancy rates and HIV rates

Created the medical affairs strategy for Merck’s HPV4 vaccine, Gardasil

….

Vaccine Approval For Children

Now, if you have time & stomach, a deeper dive into the people who unleashed the Clot Shot on babies.

DIRECTOR
Prabhakara Atreya, Ph.D.
Division of Scientific Advisors & Consultants
Center for Biologics Evaluation & Research
Food and Drug Administration – Silver Spring, MD

Dr. Prabhakara Atreya, an Indian American scientist is a 10 year veteran at the US Food and Drug Administration which she joined in 2010. Prior to this appointment, Atreya worked at the National Institutes of Health, leading the Office of Scientific Review. She has a PhD in biochemistry, biophysics and molecular biology from the Memorial University of Newfoundland, in Canada. She was one of the team of US regulators and independent experts of Vaccines and Related Biological Products Advisory Committee (VRBPAC). At the time of emergency use authorization for Pfizer’s Covid-19 vaccine, she was the Acting Designated Federal Officer of VRBPAC.
LINKED-IN

Thesis:
Atreya, Prabhakara Lakshmi (1987) Conformational aspects of proline hydroxylation in collagen biosynthesis : studies with synthetic peptides. Doctoral (PhD) thesis, Memorial University of Newfoundland.

Probable Papers (13):
Affiliation: Department of Plant Pathology, University of Kentucky, Lexington
I think this paper is what Fauci Spotted:
Construction of in-frame chimeric plant viral genes by simplified PCR strategies.
Atreya CD, Atreya PL, Pirone TP. Plant Mol Biol. 1992 Jun;19

Site-directed mutations in the potyvirus HC-Pro gene affect helper component activity, virus accumulation, and symptom expression in infected tobacco plants.
Atreya CD, Atreya PL, Thornbury DW, Pirone TP.Virology. 1992 Nov

Mutational analysis of the coat protein N-terminal amino acids involved in potyvirus transmission by aphids.
Atreya PL, Lopez-Moya JJ, Chu M, Atreya CD, Pirone TP.J Gen Virol. 1995 Feb;76
…
Her papers then show a move to NIH
Affiliation: Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892-0720, USA.
The NS1 protein of human respiratory syncytial virus is a potent inhibitor of minigenome transcription and RNA replication.
Atreya PL, Peeples ME, Collins PL.J Virol. 1998 Feb;

And then the move to FDA.
Affiliation: Laboratory of Pediatric and Respiratory Viral Diseases, DVP/CBER, Food and Drug Administration, Bethesda, MD 20892, USA.
Respiratory syncytial virus strain A2 is resistant to the antiviral effects of type I interferons and human MxA.
Atreya PL, Kulkarni S.Virology. 1999 Sep 1; (@ FDA)

Role of type I IFNs in the in vitro attenuation of live, temperature-sensitive vaccine strains of human respiratory syncytial virus.
Loveys DA, Kulkarni S, Atreya PL.Virology. 2000 Jun

……..
Her resume STINKS! She has three papers on human respiratory syncytial virus, and a bunch of early papers on cloning and tinkering with plants @ Univ Kentucky and earlier papers messing with fiber cell membranes of frog, chick, bovine, rabbit and human eye lenses @ Wayne State Univ, MI NOTHING ELSE except the Sex Card, Race Card and probably not American born.
……..

These are her picks:

CHAIR:
Hana El Sahly, M.D.
Baylor College of Medicine
May 18, 2020
Hana El Sahly on Remdesivir and the NIH’s Adaptive COVID-19 Treatment Trial (Well that answers WHO set up elders for DEATH!)

On May 15, Texas Monthly reported on their conversation with Dr. Hana El Sahly of Houston’s Baylor College of Medicine. In the coming days, she will begin registering hospitalized participants at Baylor St. Luke’s Medical Center and Ben Taub Hospital for the second phase of the National Institutes of Health’s Adaptive COVID-19 Treatment Trial, or ACTT. She’s Baylor’s lead investigator for participation in the program, which in its first phase analyzed a randomized, controlled trial designed to evaluate the safety and efficacy of the investigational antiviral remdesivir. Preliminary findings suggested that patients treated with remdesivir recovered faster than patients who received a placebo, which led to the May 1 announcement that remdesivir would be the first medication to receive FDA authorization for emergency use for COVID-19.
“We found that for patients who have COVID-19 pneumonia bad enough to get them to the hospital, treatment with remdesivir expedites the time to recovery by an average of four days per patient,” says El Sahly…
Hana El Sahly, M.D.

Education

Undergraduate education American University of Beirut, Lebannon Bachelor of Science, 1987-1990Medical education American University of Beirut, Lebannon School of Medicine, Doctor of Medicine, 1990-1994

Scientific Papers (46)

Several presentations on “HIV vaccines”
Fauci must love her:

Review Panels, Committees
Member, Safety Monitoring Committee, National Institutes of Health-sponsored vaccine clinical trial 05-0011; 2006
Reviewer, Loan Repayment Program, National Institute of Allergy and Infectious Diseases, National Institutes of Health; 2008
Member, Safety Monitoring Committee, National Institutes of Health-sponsored vaccine clinical trial 08-0009; 2009
Reviewer, Scientific Review Program, National Institute of Allergy and Infectious Diseases; 2010
Member, Data Safety Monitoring Board, Protein Sciences Corporation vaccine clinical trial PSC-22; 2010
Member, Safety Monitoring Committee, National Institutes of Health–sponsored study DMID 10-0043; 2011
Member, Safety Monitoring Committee, National Institutes of Health-sponsored study DMID 11-0007; 2011
Reviewer, Scientific Review Program, National Institutes of Health, P01 application “Towards A Universal Influenza Vaccine”; 2012
Member, Safety Monitoring Committee, National Institutes of Health sponsored study DMID 13-0087; 2014
Member, Publications Committee, Infectious Diseases Society of America; 2014-2017
Member, Safety Monitoring Committee, Mercia Pharma Inc-sponsored study NOVA MAS-1; 2015
Member of the Food and Drug Administration Vaccine and Related Biological Advisory Committee; 2016–
Reviewer, Influenza pre-applications, US Army Medical Research and Materiel Command-Congressionally Directed Medical Research Programs, 2016
WHAT THE HECK IS THIS!! => Member, ID week program planning committee, 2017-2019

Is this her daughter: Dr. Hana Mohammed Elsahly, MD 28, practicing in Houston, TX?
……

Paula Annunziato, M.D. ***
Vice President and Therapeutic Area Head
Vaccines Clinical Research
Merck
Seems to specialize in Pediatric Vaccines.
Nuv said…

…..

Archana Chatterjee, M.D., Ph.D.
Dean Chicago Medical School
Vice President for Medical Affairs
Rosalind Franklin University of Medicine and Science
M.B.B.S. (Equivalent to M.D.): Pune University, Maharashtra, India 1979-1983
Army Medical Corps, Military Hospital, Gaya, India, 1985 -1988
Major Scientific Interest: Vaccine development. She forgets to mention her main trial target is infants.

Principal Investigator: Recent Research Projects/Grants
GSK = GlaxoSmithKlinePled Guilty and Pay $3 Billion to Resolve Fraud Allegations & Failure to Report Safety Data – July 2012
(Nice people she worked for.)

Date: 2018-2019 Sponsor: Department of Health and Human Services, Administration For Community Living

Date: 2018-2020 Sponsor: Pfizer A Phase 2, Randomized,Trial ….Pneumococcal Conjugate Vaccine in Healthy Infants.

Date: 2018-2020 Sponsor: GSK …Study to Assess the Safety & Immunogenicity of Meningococcal Vaccine & 1 Pneumococcal Vaccine when Administered Concomitantly with Routine Vaccines to Healthy Infants.

Date: 2018-2020 Sponsor: GSK … dose-escalation study to evaluate safety, reactogenicity and immunogenicity of GSK Biologicals’ respiratory syncytial virus (RSV) investigational vaccine based on the RSV viral proteins F, N and M2-1 encoded by chimpanzee-derived adenovector.. when administered… to RSVseropositive infants aged 12 to 23 months.

Date: 2017-2019 Sponsor: MedImmune ….Study to Evaluate the Safety and Efficacy of MED18897, a Monoclonal Antibody With an Extended Half-life Against Respiratory Syncytial Virus, in Healthy Preterm Infants. [Are they going to give the infants the RSV?]

Date: 10/2015-10/2017 Sponsor: Merck…, Study to Evaluate the Safety, Tolerability, and Immunogenicity of Different Formulations of V114 [15-valent pneumococcal conjugate vaccine ] in Healthy Adults and Infants.

Date: 10/2015-10/2016 Sponsor: Astra Zeneca An observational study of RSV hospitalization in preterm infants.

Date: 9/2014-2017 Sponsor: GSK … multinational study … of GSK Biologicals’ MMR vaccine (209762)… compared to Merck (M-M-R®II or VaxPro), as a first dose, both co-administered with Varivax, Havrix (all subjects) and Prevnar 13 (US subset) in healthy children 12 to 15 months of age.

Peer-Reviewed Articles (120)

Appointments:
2020 – Invited to serve on NIH (NCI) Special Emphasis Panel to evaluate grant applications received in response to the RFA(s) with primary focus on HIV-Associated Malignancy Research

2019 to present – Invited to serve as and appointed a member on the Vaccines and Related Biological Products Advisory Committee (VRBPAC) of the United States Food and Drug Administration (US FDA)

2012 -2019 – Consultant to the US FDA

2014 – Merck Vision 2027 Expert Input Forum on Vaccine Policy

2008 – 2012 – Member, Anti Infective Drug Advisory Committee (AIDAC), Center for Drug Evaluation and Research, US FDA

2008 -2012 – Invited to serve on the National Vaccine Advisory Boards for Merck, GlaxoSmithKline and Novartis Pharmaceutical Companies

2008– Merck Vaccination Service Award, recognition of commitment to improving public health through vaccination.

2006 – Invited member, Sanofi-Pasteur, MedImmune, Abbott Pharmaceutical Companies’ National Advisory Boards

2003 – Invited Session Chair at an International Symposium organized by the Merieux Foundation entitled, “Vaccination in Tomorrow’s Society – New Information Pathways”. Annecy, France

Merieux Foundation …. AND THAT GETS INTERESTING…. WIKI

In October 2004, the FM was the beneficiary of a Franco-Chinese agreement that led to the creation of the Institut Pasteur de Shanghai.…
In 2012, the FM continued its partnership with the Chinese Academy of Medical Sciences.
In 2015, the CAMS-FM partnership founded the Christophe Mérieux Laboratory (CML) at the Institute of Pathogen Biology in Beijing to focus on the study pneumonia and tuberculosis. Researchers at the CML “benefit from and training modules developed by the Emerging Pathogens Laboratory in Lyon”,[5][6] a BSL-4 lab which was also built by the FM in 1999 and since 2005 is now operated by INSERM.[7]
In 2015, the FM participated in the donation by the French government of CIRI’s Biosafety Level 4 expertise to the Wuhan Institute of Virology.
In January 2017, a researcher who was financed by the CAMS-FM partnership participated in a study of human rhinovirus and genotype A21…..
https://en.wikipedia.org/wiki/Fondation_M%C3%A9rieux
WIKI

“Mentorship and sponsorship of faculty and learners has been a hallmark of Dr. Chatterjee’s entire thirty- year career in academic medicine…” LINK [I am sure she has been kissing FauXi’s ass for years to get funding.]
MORE:

….Board certified in general pediatrics and pediatric infectious diseases, she is nationally recognized for her work in vaccine development for human papilloma viruses and in antibiotic resistance. She has completed more than 100 clinical trials and published more than 50 peer-reviewed articles, 23 invited review articles, 17 book chapters and one book.
The first woman and person of color to serve as dean of CMS, Dr. Chatterjee, a native of India, earned her medical degree from the Armed Forces Medical College at Pune University in India and her PhD from the University of Nebraska Medical Center (UNMC) in Omaha….
https://www.rosalindfranklin.edu/news/rfu-announces-selection-of-new-dean-for-chicago-medical-school/

…..

CAPT Amanda Cohn, M.D.
Expertise: Pediatrics, Vaccines
Chief Medical Officer
National Center for Immunizations and Respiratory Diseases
Centers for Disease Control and Prevention

Immunization and Respiratory Diseases (NCIRD) MISSION | CDC
The mission of the National Center for Immunization and Respiratory Diseases (NCIRD) is the prevention of disease, disability, and death through immunization and by control of respiratory and related diseases.
CDC

POSTGRADUATE TRAINING 2004 – 2006 Epidemic Intelligence Service, CDC, Atlanta, GA
WORK EXPERIENCE :
3/2019-present Chief Medical Officer (Acting), Vaccine Policy, Preparedness, and Global Health, Office of the Director, NCIRD, CDC
11/2015-present Executive Secretary, ACIP and Senior Advisor, Vaccines Office of the Director, NCIRD, CDC
5/2014-11/2015 Deputy Division Director, Immunization Services Division, NCIRD, CDC
01/2013-05/2014 Acting Epidemiology Team Lead Meningitis and Vaccine Preventable Diseases, DBD, NCIRD, OD
06/2006-12/2012 Medical Officer, Epidemiology Team Meningitis and Vaccine Preventable Diseases, Division of Bacterial Disease, NCIRD, CDC
07/2004-06/2006 Epidemic Intelligence Service (EIS) Officer, Epidemiology Program Office Centers for Disease Control and Prevention, Atlanta, GA Assigned to: Bacterial Vaccine Preventable Diseases Branch, National Immunization Program

Scientific papers: 59 many authored with Nancy E Messonnier
Great titles like:

Multistate Outbreak of Respiratory Infections Among Unaccompanied Children, June 2014-July 2014.
Conclusions: This respiratory disease outbreak was due to multiple pathogens, including Streptococcus pneumoniae serotype 5 and influenza viruses. Pneumococcal and influenza vaccinations prevented further transmission. Future efforts to prevent similar outbreaks will benefit from use of both vaccines. https://pubmed.ncbi.nlm.nih.gov/27001799/
[How about CLOSING THE DARN BORDERS!]
Understanding Factors Affecting University A Students’ Decision to Receive an Unlicensed Serogroup B Meningococcal Vaccine.
Compliance with recommendations and opportunities for vaccination at ages 11 to 12 years: evaluation of the 2009 national immunization survey-teen.
Adolescent immunizations and other clinical preventive services: a needle and a hook?
Immunizations in the United States: a rite of passage.
Attitudes, practices, and preferences of pediatricians regarding initiation of hepatitis B immunization at birth.
……

Hayley Gans, M.D.
Expertise: Pediatrics, Infectious Diseases
Professor of Pediatrics
Department of Pediatrics
Stanford University Medical Center

Fellowship: Stanford University School of Medicine (1998) CA

Medical Education: State University of New York Syracuse Medical School Registrar (1991) NY
Board Certification: American Board of Pediatrics, Pediatric Infectious Diseases (1999)
Residency: Stanford University Medical Center (1994) CA
Internship: Stanford University Medical Center (1992) CA
M.D., SUNY at Syracuse, Medicine (1991)

Fellowship Program Director, Pediatric Infectious Diseases (2006 – 2017)

Co-director, Pediatric Infectious Diseases Program for Immunocompromised Hosts, Children’s Hospital at Stanford (2013 – Present)
Associate Fellowship Director, Pediatric Infectious Diseases, Stanford University Medical Center (2017 – Present)
Director, Fellowship Education, Department of Pediatrics, Stanford University Medical Center (2017 – Present)

Sort of BLAAaaaah until you look at this paper:

Remember her focus is kids.

July 2020 Lancet preprint.
Kinetics of SARS-CoV-2 Positivity of Infected and Recovered Patients: A Single Center COVID-19 Experience and Potential Implications https://autopapers.ssrn.com/sol3/papers.cfm?abstract_id=3605268

Jia Huang – Southern University of Science and Technology CHINA and 42 other authors with only 7 others not Chinese. The other universities were Sichuan University, China and Sanford.

https://autopapers.ssrn.com/sol3/cf_dev/AbsByAuth.cfm?per_id=4257785

And then it REALLY GETS GOOD:

FUNDING STATEMENT: This work was supported by grants from Sanming Project of Medicine in Shenzhen (Jia Huang, No. SZSM201812065); Bill & Melinda Gates Foundations (Lei Liu); and from National Natural Science Foundation of China (Jia Huang, No. 81501651)

DECLARATION OF INTERESTS: The authors declare no competing interests.

ETHICS APPROVAL STATEMENT: This study was approved by the Ethics Committee of the Second Affiliated Hospital of Southern University of Science and Technology.[CHINA]

Abstract

BACKGROUND: Recurrence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) positive detection in infected but recovered individuals has been reported. Patients who have recovered from coronavirus disease 2019 (COVID-19) could profoundly impact the health care system if a subset were to be polymerase chain reaction (PCR)-positive again with reactivated SARS-CoV-2. We sought to define the kinetics and relevance of PCR-positive recurrence during recovery from acute COVID-19 to better understand risks for prolonged infectivity and reinfection.

METHODS: A series of COVID-19 414 patients, at The Second Affiliated Hospital of Southern University of Science and Technology in Shenzhen, China from January 11 to April 23, 2020. Univariable and multivariable statistical analysis of inpatient data were performed to develop an algorithm to predict patients at risk of recurrence of PCR positivity.
[REMEMBER PCR TESTS RETURN MAJOR FALSE POSITIVES – Reiner Fuellmich say this guy Droston isn’t a Doctor at all, but a bull**** artist. Christian Drosten & the Fraud Behind COVID 19 PCR Testing ]
FINDINGS: 16·7% recovered patients with PCR positive recurring one to three times, despite being in strict quarantine. Younger patients with mild pulmonary respiratory syndrome had higher risk of PCR positivity recurrence. The recurrence prediction model had an area under the ROC curve of 0·786.

INTERPRETATION: This case series provides clinical characteristics of recovered COVID-19 patients with recurrent SARS-CoV-2 positivity, despite strict quarantine, at a 16·7% rate. Use of a recurrence prediction algorithm may identify patients at high risk of recurrent SARS-CoV-2 positivity and help understand reactivation and reinfection possibilities to establish protocols for health policy.
LANCET

This is a very important paper because it REFUTES NATURAL IMMUNITY and green lights MORE DRACONIAN ECONOMY KILLING ‘Health Measures’

……

Holly Janes, Ph.D.
Expertise: Biostatistics
Professor — Fred Hutchinson Cancer Research Center
Vaccine and Infectious Disease Division
Division of Public Health Sciences – Seattle, WA

Dr. Holly Janes is a biostatistician working on the design and analysis of vaccine studies, with a particular expertise in HIV prevention and vaccine science. She also develops and applies statistical methodology for evaluating biomarkers for risk prediction and optimizing treatment decisions

Current Projects

Leadership for the Statistical Data Management Center of the HIV Vaccine Trials Network

Statistical methods for HIV prevention efficacy trials

Statistical methods for human challenge studies

Statistical evaluation of biomarkers for making treatment decisions https://www.fredhutch.org/en/faculty-lab-directory/janes-holly.html

HONORS, AWARDS, SCHOLARSHIPS:

2008 Travel Award, AIDS Vaccine Conference, Global HIV Vaccine Enterprise

2000 Cardiovascular Biostatistics Training Grant, National Institutes of Health

EDITORIAL RESPONSIBILITIES:

Associate Editor Journal of the National Cancer Institute (2015-2018)

Diagnostic and Prognostic Research (2016-present)

Statistical Communications in Infectious Diseases (2019-present)

RESEARCH FUNDING:

Active Funding:

2 UM1 AI068635 (PI: Gilbert P) 01/01/2014 – 11/30/2020 5.4 Calendar NIH/NIAID SDMC HIV Vaccine Trials Network

2 R01 CA152089 (PI: Janes H) 07/01/2010 – 11/30/2021 4.8 Calendar

NIH/NCI

Statistical Methods for Evaluating Markers for Treatment Selection

Interventions for disease treatment and prevention can potentially be made more cost-effective by using markers to identify in advance the individuals most likely to benefit from the treatment, and thus avoid treating those unlikely to benefit. [Rationed Health Care anyone?]

Lots more Mostly NIH and then this goodie:

38744 7/1/2006-4/30/2012

Bill & Melinda Gates Foundation

Vaccine Immunology Statistical Center (VISC) The VISC will provide 1) statistical and study design support for pre-clinical vaccine performance trials, 2) centralized data management services for the standardized evaluation of vaccine candidates, 3) development of new statistical methods for cross-species correlates-of-protection analysis.

Role: Faculty Statistician

BIBLIOGRAPHY Publications in Refereed Journals

1. Pepe MS, Janes H, Longton G, Leisenring W, Newcomb P. Limitations of the odds ratio in gauging the performance of a diagnostic, prognostic, or screening marker. Am J Epidemiol. 2004;159(9):882-90.

2. Janes H, Pepe M, Kooperberg C, Newcomb P. Identifying target populations for screening or not screening using logic regression. Stat Med. 2005;24(9):1321-38.

12. McElrath MJ, De Rosa SC, Moodie Z, Dubey S, Kierstead L, Janes H, Defawe OD, Carter DK, Hural J, Akondy R, Buchbinder SP, Robertson MN, Mehrotra DV, Self SG, Corey L, Shiver JW, Casimiro DR. HIV-1 vaccine-induced immunity in the test-of-concept Step study: A casecohort analysis. Lancet. 2008;372(9653):1894-905. PMCID: 2774110.

13. Pepe MS, Feng Z, Janes H, Bossuyt PM, Potter JD. Pivotal evaluation of the accuracy of a biomarker used for classification or prediction: Standards for study design. J Natl Cancer Inst. 2008;100(20):1432-8. PMCID: 2567415.

21. Barnabas RV, Wasserheit JN, Huang Y, Janes H, Morrow R, Fuchs J, Mark KE, Casapia M, Mehrotra DV, Buchbinder SP, Corey L. Impact of herpes simplex virus type 2 on HIV-1 acquisition and progression in an HIV vaccine trial (the Step study). J Acquir Immune Defic Syndr. 2011;57(3):238-44. PMCID: 3446850.

22. Fitzgerald DW, Janes H, Robertson M, Coombs R, Frank I, Gilbert P, Loufty M, Mehrotra D, Duerr A. An Ad5-vectored HIV-1 vaccine elicits cell-mediated immunity but does not affect disease progression in HIV-1-infected male subjects: Results from a randomized placebo-controlled trial (the Step study). J Infect Dis. 2011;203(6):765-72. PMCID: 3119328.

And many more. I am sure Fauci loves her.

……

Michael Kurilla, M.D., Ph.D.
Expertise: Infectious Diseases, Pathology
Director, Division of Clinical Innovation
National Center for Advancing Translation Sciences
National Institutes of Health

National Center for Advancing Translational Sciences

The National Center for Advancing Translational Sciences (NCATS) is one of 27 Institutes and Centers at the National Institutes of Health (NIH). The focus of NCATS is to advance the science of translation, which is the process of turning observations into interventions to improve health.
National Center for Advancing Translation Sciences

……

Myron Levine, M.D., D.T.P.H., F.A.A.P
Expertise: Infectious Diseases

Simon & Bessie Grollman Distinguished Professor
Associate Dean for Global Health
Vaccinology and Infectious Diseases Center for Vaccine Development
University of Maryland School of Medicine

Center for Vaccine Development and Global Health – UMB …

University of Maryland School of Medicine

For more than a year, researchers at the Center for Vaccine Development and Global Health (CVD) at the University of Maryland School of Medicine (UMSOM) have been working tirelessly on COVID-19 research, helping to pave the way for the use of vaccines and therapies that are being administered across the country.
Under the leadership of CVD director Kathleen Neuzil, MD, MPH, FIDSA, the Myron M. Levine, MD, DTPH, Professor in Vaccinology at UMSOM, researchers quickly pivoted decades of vaccine and infectious disease research experience toward combating this deadly virus, which continues to impact millions of people around the world.
Faculty at CVD have served in critical leadership roles in U.S. and international research and policy efforts. For example, Neuzil co-chaired the COVID-19 Prevention Trials Network, a research network established by the National Institute of Allergy and Infectious Diseases [NIAID Dr. Fauciwas appointed director of NIAID in 1984.] in response to the pandemic. Vaccine research at CVD continues, with an emphasis on reaching the populations most impacted by COVID-19 and testing pediatric vaccines.
CVD experts have launched an expansive grassroots campaign to educate the community and reach those who have been hit the hardest by this terrible virus, including members of the Black and Brown communities, the elderly, and those with underlying health risks.
“Our CVD team has worked tirelessly and meticulously to advance COVID-19 vaccines and to ensure they are reaching the most affected populations,” Neuzil said. “Our work continues as we begin testing vaccines in children and investigate booster vaccines to address the risk of COVID-19 variants.” [Like this Dude is neutral?]

Center for Vaccine Development and Global Health (CVD …

Our research, surveillance and vaccine development focuses on four key areas: Enteric Diseases, Malaria, Influenza and Respiratory Diseases, and Emerging Pathogens.
Overview
Our faculty and staff are experts in the field of global health and vaccinology, and they are dedicated to improving global health by conducting innovative, world-leading research in Baltimore and around the world. Our key mission is to harness the power of vaccines to prevent disease and save lives in the most vulnerable populations.

…….

H. Cody Meissner, M.D.
Expertise: Infectious Diseases
Professor of Pediatrics
Tufts University School of Medicine
Director, Pediatric Infectious Disease
Tufts Medical Center
POST GRADUATE TRAINING

1973 – 1975 Internship and Residency Boston Floating Hospital New England Medical Center Boston, MA

1975 – 1977 Research Associate Public Health Service National Institute of Child Health and Human Development National Institute (NICHD) Bethesda, MD Parent Agency is National Institutes of Health (Fauci)

2008 – Present Advisory Committee on Immunization Practices (ACIP) Centers for Disease Control and Prevention (CDC)

2010 – Present Massachusetts Vaccine Purchasing Advisory Council

2017 – Present National Vaccine Advisory Committee, United States Department of Health and Human Services

2017 – Present Vaccine Injury Compensation Program, United States Department of Health and Human Services

AWARDS

Massachusetts 2017 Recipient of the CDC Childhood Immunization Award

The National Vaccine Injury Compensation Program: Striking a Balance Between Individual Rights and Community Benefit.

Meissner HC, Nair N, Plotkin SA. JAMA. 2019 Jan 29

The Importance of MMR Immunization in the United States.

Perrone O, Meissner HC. Pediatrics. 2020 Aug

Principles of Vaccine Licensure, Approval, and Recommendations for Use.

Pickering LK, Meissner HC, Orenstein WA, Cohn AC. Mayo Clin Proc. Epub 2020 Feb 13.

H. Cody Meissner, MD | Tufts Medical Center

H. Cody Meissner, MD, is a leading national expert on childhood vaccinations who consults with the Centers for Disease Control and Prevention on periodic updates to the recommended immunization schedule for newborns through 18-year-olds. At Tufts Children’s Hospital at Tufts Medical Center he heads the Division of Pediatric Infectious Diseases

….

Paul Offit, M.D.
Expertise: Infectious Diseases
Professor of Pediatrics
Division of Infectious Diseases
The Children’s Hospital of Philadelphia

Paul A. Offit, MD is the Director of the Vaccine Education Center at the Children’s Hospital of Philadelphia as well as the Maurice R. Hilleman Professor of Vaccinology and a Professor of Pediatrics at the Perelman School of Medicine at the University of Pennsylvania. He is a recipient of many awards including the J. Edmund Bradley Prize for Excellence in Pediatrics from the University of Maryland Medical School, the Young Investigator Award in Vaccine Development from the Infectious Disease Society of America, and a Research Career Development Award from the National Institutes of Health. Dr. Offit has published more than 160 papers in medical and scientific journals in the areas of rotavirus-specific immune responses and vaccine safety. He is also the coinventor of the rotavirus vaccine, RotaTeq, recommended for universal use in infants by the CDC….
FDA

In 2017, Dr. Offit was a weekly columnist for The Daily Beast.

Papers:

2018

Plotkin, S.A., P.A. Offit, and P. Bégué, : “Vaccine mandates in France will save lives,” Science 359: 283-284, 2018.

Plotkin SA, Offit PA, Reiss D.: Important New Resource for Clinicians Giving Expert Witness Testimony on Vaccines. Pediatr Infect Dis J. 37(12), Dec. 2018.

To the Editors:

Vaccination is under attack by individuals who occasionally use the legal system to oppose mandatory vaccination laws and in some cases to obtain exemptions for particular children whose parents are opposed to vaccination. During the legal proceedings, as we have witnessed, experts testifying in favor of vaccination may be challenged with references from journals of doubtful quality that oppose vaccination.
To provide important references that discuss and disprove claims made against vaccines, the Vaccine Education Center at the Children’s Hospital of Philadelphia has created a library of references addressing certain safety issues that may be useful as an aid and refresher to clinicians giving expert testimony on the safety of vaccines and to lawyers defending vaccination of children.
The Children’s Hospital of Philadelphia legal library may be entered through the web address vaccine.chop.edu/safety-references.
We would be grateful if you could inform your colleagues about the availability of this resource, which should be of great value for experts testifying for vaccination and for clinicians who need to convince parents about vaccine safety. https://journals.lww.com/pidj/Fulltext/2018/12000/Important_New_Resource_for_Clinicians_Giving.42.aspx

2017

Offit, P.A.: “Commentary: Science Denialism Isn’t New to the Trump Administration,” Philadelphia Inquirer December 22 2017.

Offit, P.A.: “By Regulating Homeopathic Remedies, FDA Holds ‘Modern-Day Snake-Oil Salesmen’ Accountable,“ Philadelphia Inquirer December 28 2017.

2013

Williams SE, Rothman RL, Offit PA. Schaffner W, Sullivan M, Edwards KM. A randomized trial to increase acceptance of childhood vaccines by vaccine-hesitant parents: a pilot study. Academic Pediatrics (2013) 13: 475-480.

A look at his recent papers shows he is targeting vaccine hesitant parents.

https://pubmed.ncbi.nlm.nih.gov/?term=Offit+PA&cauthor_id=24011750&size=20

…..

Steven Pergam, M.D.
Expertise: Infectious Diseases
Medical Director
Infection Prevention
Seattle Cancer Care Alliance — Seattle, WA

He seems to specialize in cancer and immuno-compromised and seems to be the best of a bad bunch. But then we look at this:

SPECIAL NATIONAL RESPONSIBILITIES:

2009–2010 Independent Safety Monitor, NIH/NIAD, DMID Influenza Protocols: 09-0039, 09-0043, 09-0047, 09-0053, and 09-0054: H1N1

2010–2011 Independent Safety Monitor, NIH/NIAID, DMID Protocol 09-0002: Comparison of the Safety and Immunogenicity of Lyophilized IMVAMUNE® (1×108 TCID50) versus Liquid Formulation IMVAMUNE® (1×108 TCID50) Administered by the Subcutaneous Route and a Lower Dose Liquid Formulation IMVAMUNE® (2×107 TCID50) Administered by the Intradermal Route in Healthy Vaccinia-Naïve Individuals (Bavarian Nordic)

2011–2013 Member, Data and Safety Monitoring Board: Effect of tenofovir on genital HSV shedding: a randomized, double-blind, placebo-controlled, clinical trial

2015-present Member, Zoster Working Group, Advisory Committee on Immunization Practices (ACIP), Centers for Disease Control and Prevention, Department of Health and Human Services

2016-present Member, Abstract Selection Committee, Association for Professionals in Infection Control and Epidemiology (APIC)

2016-2017 Independent Safety Monitor, NIH/NAID, DMID Protocol 16-0117: Comparison .of High vs. Standard Dose Flu Vaccine in Pediatric Stem Cell Transplant Recipients

15. RESEARCH FUNDING

Current: Washington Vaccine Alliance (WAVA) Pilot Award (PI: S. Pergam) 10/1/13-6/30/20 Interactions between gastrointestinal microbiota, Influenza vaccine responses and respiratory viral infections in a large cohort of clinic employees

BAA-NIAID [Fauxi Director]-DMID-NIH-AI (PI: M. Ison; Subcontract PI: Pergam) 5/1/16-4/30/20 Phase II Multi-Center, Prospective, Randomized, Double-Blind Study of Nitazoxanide in Acute and Chronic Norovirus in Hematopoietic Stem Cell and Solid Organ Transplant Recipients 1U01AI132004-NIAID (PI: N.Halasa; Subcontract PI: Pergam)

7/5/2017-6/30/20 High vs. Standard Dose Flu Vaccine in Adult Stem Cell Transplant Recipients 1R01AI134808-NIAID (PI: D. Fredricks)

Completed:

NIH/NIAID T32 AI007-044 (PI: W. Stamm) 9/1/05-2/1/07 Host Defense Training in Allergy and Infectious Diseases

Industry Sponsored Clinical Trials:

Chimerix, Inc. (PI: Pergam) 2016-current An Intermediate-size, Expanded Access Protocol to Provide Bincidofovir for the Treatment of Serious Adenovirus Infection or Disease, Protocol CMX001-35”

6/17/2017-present Prior Industry Trials Merck, Sharp & Dohme Co., Inc (PI: Pergam)

2012-2015 Pergam, SA – CV Page 15 A Phase III, Double-Blind, Randomized, Placebo-Controlled, Multicenter Clinical Trial to Study the Safety, Tolerability, Efficacy, and Immunogenicity of V212 in Recipients of Autologous Hematopoietic Cell Transplants (HCT)

Cubist Pharmaceuticals, Inc.* (PI: Pergam) 2013-2015 A Phase IIIb, Multi-Center, Double-Blind, Randomized, Placebo-Controlled Study to Demonstrate the Safety & Efficacy of Fidaxomicin for Prophylaxis against C difficile-Associated Diarrhea in Individuals Undergoing Hematopoietic Cell Transplants (HCT) *formerly Optimer pharmaceuticals

KRT16/26/21, 01:40 PM

$ACXP In December 2014, Merck ($MRK) paid US$9.5 billion for Cubist ($CBST) largely to obtain marketing access to agents daptomycin and fidaxomicin. https://stocktwits.com/symbol/CBST

Chimerix, Inc. (PI: Pergam) 2016 A Multicenter Non-Interventional Study to Obtain Retrospective Data for Subjects Previously Diagnosed with Adenovirus Infection to serve as Matched Historical Controls for Study CMX001-304; Protocol No. CMX001-305

Chimerix, Inc. (PI: Pergam) 2015 – 2017 A Phase 3, Open-label, Multicenter Study of the Safety/Tolerability and Efficacy of Brincidofovir (CMX001) for the Prevention of Adenovirus (AdV) Disease in Subjects with Asymptomatic AdV Infection at Risk of Progression and for the Treatment of Subjects with Localized or Disseminated AdV Disease

Chimerix, Inc.

All that shimmers isn’t … enhanced by lipid conjugate technology. Chimerix is a development-stage biopharmaceutical company, dedicated to accelerating the advancement of innovative for patients living with cancer and other serious diseases. Its two clinical-stage development programs include dociparstat sodium (DSTAT) and brincidofovir (BCV). DSTAT, is a glycosaminoglycan derivative of heparin with known anti-inflammatory properties and BCV is an oral antiviral in development for the treatment of smallpox.

2505 Meridian Pkwy Ste 100 Durham, NC,

https://www.dnb.com/business-directory/company-profiles.chimerix_inc.a1878daaef1b59d25a1d2e8876c4b4bf.html

Chimerix, Inc.’s key principal is Michael A Sherman. Chimerix, Inc. has 54 employees

https://wallmine.com/people/8557/michael-a-sherman

…..

Jay Portnoy, M.D.
Expertise: Consumer Representative (This the guy who is supposed to represent the interests of the Public.)
Professor of Pediatrics
Medical Director of Telemedicine Section of Allergy, Asthma and Immunology
Children’s Mercy Hospital Kansas City, MO

Offices and Board of Directors:

American Board of Allergy & Immunology (ABAI). 2014-present.

Vice President, American College of Allergy, Asthma & Immunology 2005-6.

Board of Directors, Black Healthcare Coalition. 2006-2009. [He is WHITE]

Editorships and Editorial Boards

Regional Editor, World Allergy Organization Journal. 2008 to 2012.

Section Editor, Annals of Allergy and Asthma. Appointed 2002 to 2005

Editor, Current Opinion on Allergy & Asthma. Issue on Pediatric Allergy. 2004 and 2005

Editor, Current Allergy and Asthma Reports. Issue on Pediatric Allergy. 2001-2013

Editorial Board, Allergy Watch. 1998-2001.

Editorial Board, Annals of Allergy and Asthma. 1994 to 2006

Editorial Board, Current Allergy Practice. 1993 to present

Other Appointments

FDA advisory panel (CBER), Allergenic Extracts.

2017-present FDA advisory panel (CDER). Respiratory and allergy drugs.

2010-present FDA advisory panel (CBER), Allergenic Extracts.

2005-2010 Special Emphasis Panel. T-cell Epitopes. NIAID. 2011.

https://www.fda.gov/media/105541/download

The guy has 151 papers mainly dealing with allergy so I am not going to look at all of them.

He seems to work with Environmental Allergens Workgroup. Also with American College of Allergy, Asthma & Immunology – “…a professional medical association of more than 6,000 allergist-immunologists and allied health professionals…” He is a Fellow, American Academy of Allergy, Asthma, and Immunology (AAAAI) …. if you search long enough…. You find an AAAAI Legislative Action article urging Allergists to support Fauci’s funding.

NIAID, NIEHS, NHLBI, MCAN Workshop Report: The Indoor Environment and Childhood Asthma: Implications for Home Environmental Intervention in Asthma Prevention and Management

The National Institute of Allergy and Infectious Diseases (NIAID), National Institute of Environmental Health Sciences (NIEHS), National Heart, Lung, and Blood Institute (NHLBI), and Merck Childhood Asthma Network (MCAN) sponsored a joint workshop to discuss the current state of the science with respect to the indoor environment and its effects…

Adverse reactions to vaccines practice parameter 2012 update

…..Thus although patients with a history of mild reactions to egg ingestion (hives only) can receive their vaccine in a primary care provider’s office, those with a history of more severe reactions (cardiovascular, respiratory, or gastrointestinal symptoms) should receive the influenza vaccine in an allergist’s office. In both cases, personnel to recognize and equipment to treat anaphylaxis need to be immediately available, but the allergist’s office affords additional expertise in this area should it be required…..
…..There has been a great deal of additional information published over the past year demonstrating the safety of influenza vaccination in patients with egg allergy. Health care providers should no longer withhold the vaccine from any patient with egg allergy. In an update to recommendations made in the last year, it is now considered safe for patients even with a history of a severe egg allergy to receive influenza vaccination…..

No worries, we will revive you when you almost die of anaphylaxtic shock, it is utmost importance for us to jab you with a shot that is probably useless so we can get paid our bonus.
…..

Andrea Shane, M.D., M.P.H., M.Sc.
Expertise: Pediatric & Infectious Diseases

Professor of Pediatrics
Director Division of Pediatric Infectious Diseases
Emory University School of Medicine – Atlanta, GA

Joint appointment:
Assistant Professor of Global Health Hubert Department of Global Health, Rollins School of Public Health, Emory University 01 September 2013-present

Military or Government Service: Lieutenant Commander, United States Public Health Service, 2001-2003; Inactive Reserve Corps (IRC) 2003-until IRC dissolved in 2010.
……
The United States Public Health Service is a collection of agencies of the Department of Health and Human Services concerned with public health, containing eight out of the department’s eleven operating divisions. The Assistant Secretary for Health oversees the PHS.
WIKI

ALSO:

OASH oversees the Department’s key public health offices and programs, a number of Presidential and Secretarial advisory committees, 10 regional health offices across the nation, and the Office of the Surgeon General and the U.S. Public Health Service Commissioned Corps. https://www.hhs.gov/ash/index.html
……

Centers for Disease Control and Prevention, Advisory Committee on Immunization Practices (ACIP) respiratory syncytial virus (RSV) immunoprophylaxis working group, appointed member, 2009-until committee dissolved by CDC in 2011.

Infectious Diseases Society of America (IDSA) National Global Public Health Committee (NGPHC), appointed member 2010-2013.

World Society of Pediatric Infectious Diseases (WSPID), Board Member and member of the Education Committee representing the Pediatric Infectious Disease Society (PIDS), appointed 2017; term through 2019.

[THIS IS WHERE SHE HAS A LOT OF POWER]
Manuscript reviewer:
American Journal of Infection Control, 2001-2003
Clinical Infectious Disease Journal, 2003-present
Journal of Infectious Diseases, 2003 – present
Pediatrics, 2006 – present
Journal of Pediatrics, 2006-present
The Pediatric Infectious Disease Journal, 2003-present
Infection Control and Hospital Epidemiology, 2003 – present
Archives of Pediatrics and Adolescent Medicine, 2006 – present
Emerging Infectious Diseases Journal, 2006 – present
Neonatology, 2008 – 2010
Journal of American Medical Association, 2009 – present
JAMA Pediatrics, 2013 – present
Journal of Pediatric Infectious Diseases, 2013-present
Pediatric Research 2017-present
Clinical Therapeutics, 2017-present
Faculty of 1000 (f1000), Public Health and Epidemiology section, post publication peer review of publications, 2009 -2011. [WTF???]
Pediatric Infectious Disease section with creation of the section, 2011-2014.

Honors and Awards:
International exchange fellowship, Children’s Hospital at Montefiore and Beijing Children’s Hospital, Beijing, China October-November, 1999

Department of Health and Human Services, Public Health Service Crisis Response Service Award, 2002

Department of Health and Human Services, Public Health Service Outstanding Unit Citation, 2002

National Foundation for Infectious Diseases (NFID) Advanced Vaccinology Course Travel Grant to attend ADVAC 9, Annecy, France, 2008

National Institute of Allergy and Infectious Diseases, Division of Microbiology and Infectious Diseases, Special Recognition, H1N1 influenza research, 2010

Center for Disease Control and Prevention, National Center for Emerging and Zoonotic Infectious Diseases Award for Excellence in Partnering-Domestic to NETEC (the National Ebola Training and Education Center)…. This award recognizes programs’ initiative and effectiveness through establishing and sustaining a strategic partnership with government, private sector, volunteer, or nonprofit organizations, 24 March 2016.

Contracts:

Co- investigator, NIH/NIAID/DMID Vaccine and Treatment Evaluation Unit (VTEU) – Emory University School of Medicine. Role: Site PI on rotavirus vaccine cross-over trial, DMID #08- 0017 and influenza vaccine to breastfeeding women trial, DMID#09-007; site co- investigator on other trials. Salary support, 01 August 2007- 01 August 2016….

………….

Paul Spearman, M.D.
Expertise: Pediatric & Infectious Diseases

Director, Division of Infectious Diseases
Albert B. Sabin Chair in Pediatric Infectious Diseases
Cincinnati Children’s Hospital Medical Center
Professor, Department of Pediatrics
University of Cincinnati School of Medicine Cincinnati, OH

This guy is a really big heavy weight. There is cross-over with the lady, Andrea Shane above. Any bets he pulled her in to be his ‘female puppet’ – a good little government soldier?

11/2005-09/2016: Professor and Division Director Nahmias-Schinazi Research Chair Pediatric Infectious Diseases Department of Pediatrics Emory University School of Medicine
11/2005-09/2016: Associate Director for Pediatric Studies Emory Vaccine Center Atlanta, GA
03/2009-09/2016: Vice Chair for Research Department of Pediatrics Emory University School of Medicine
03/2009-09/2016: Chief Research Officer Children’s Healthcare of Atlanta Atlanta, GA

[Andrea L. Shane is Attending Pediatrician Children’s Healthcare of Atlanta Emory Healthcare Grady Health 01 August 2006 – present ]

This guy has a full page of
COMMITTEE MEMBERSHIPS:
a. National and International:

NIH Councils and Study Sections Chair, NIH ZRG1 AARR-E (41)
December 2016 Member, NIH ZRG1 AARR-P (02)
December 2016 Chair, NIH SEP: ZRG1 AARR-K (02)M; AIDS and related research SEP
August 2016 Chair, NCI Board of Scientific Counselors, Site Visit Team, Review of HIV DRP, Frederick, MD
July 2016 Chair, NIH SEP: ZDE1; Approaches to Eliminate HIV and Opportunistic Pathogens from Oral Reservoirs
November 2015 Chair, NIH SEP: ZRG1 AARR-E; AIDS and AIDS-related
July 2015 Chair, NIH SEP: Basic Research on HIV Persistence
March 2015 Chair, NIH/NIDCR Review Panel on HIV and Oral
March 2015 Opportunistic Pathogens
.
.
.

NIH/NIAID HIV Vaccine Trials Network
Protocol Chair, HVTN 088 Protocol 2010-present
Chair, Chiron/Novartis Products Development Team 2000-2007
Chair, Wyeth Products Development Team 2001-2007 Protocol
Chair, HVTN 049 Protocol 2002-2007 Protocol
Chair, HVTN 056 Protocol 2002-2006 Protocol
Chair, HVTN 061 Protocol 2003-2005 Member, HVTN Phase I-II Committee 2002-2005 Protocol
Chair, HVTN 088 Protocol 2010-present
NIH/NIAID/DMID Vaccine and Treatment Evaluation Unit Co-Principal Investigator, Emory VTEU site 2007-present
Protocol Chair, VTEU 0008 Protocol 2009-2014
NIH/NICHD-Westat/NIAID IMPAACT Network Principal Investigator, Emory IMPAACT site 2014-present
.
.
.
CONSULTANTSHIPS:
Chiron, HIV Vaccines Development Team, Emeryville, CA 2003, 2004
Wyeth, HIV Vaccine Programs, Pearl River, NY 2003, 2004

EDITORSHIPS AND EDITORIAL BOARDS: [Again this is where a lot of power lies.]
Member of Editorial Board, Journal of Virology
Member of Editorial Board, Virology
Member of Editorial Board, Current HIV Research
Academic Editor, PLoS One

MANUSCRIPT REVIEWER: [There is that POWER again]
Journal of Virology (numerous, 1995-present)
Virology (numerous, 1998-present)
Current HIV Research (2001-present)
Ad Hoc reviewer, Biochemistry (2005, 2006)
Ad Hoc reviewer, Traffic (2005, 2006, 2007, 2013)
Ad Hoc reviewer, JAIDS (2004, 2011, 2012, 2013, 2014, 2015)
Ad Hoc reviewer, JBC (1997-present)
Ad Hoc reviewer, Leukocyte Biol (2000)
Ad Hoc reviewer, Vaccine (2000-2016)
Ad Hoc reviewer, Virus Research (2005, 2012, 2012, 2013)
Ad Hoc reviewer, Nature Structural Biology (2005)
Ad Hoc reviewer, PLOs Medicine (2006, 2007, 2008)
Ad Hoc reviewer, J Mol Biol (2007,2012, 2015, 2016)
Ad Hoc reviewer, PNAS (2007, 2008, 2009,2012, 2013, 2014)
Ad Hoc reviewer, JCB (2007, 2008, 2010, 2011,2012, 2013)
Ad Hoc reviewer, PLOs One (2008, 2009, 2010,2011,2012, 2013, 2014) 6
Ad Hoc reviewer, Cell Host and Microbe (2008-present)
Ad Hoc reviewer, Nature Medicine (2009, 2011,2012, 2016)
Ad Hoc reviewer, PLOs Pathogens (2009-present) Ad Hoc reviewer, J Immunology (2010, 2011, 2013) Ad Hoc reviewer, Retrovirology (2011-present)
.
.
GRANT SUPPORT:
a. Active Support

Federally funded:
NIH R01 AI058828: Role of Vpu in HIV Particle Assembly. Funded since 2004, currently in no-cost extension with competing renewal under review.
NIH R01 GM111027-17A1: Viral and Cellular Determinants of HIV-1 Assembly. Funded 9/16/2013-8/31/2017 (Principal Investigator). $200,000 initial period; $800,000 direct costs.
NIH R01AI11863: Mucosal Protection against HIV Generated by PIV5 Priming and VLP Boosting. Funded 4/01/2014-8/31/2018 (Principal Investigator, Multiple PI grant). $351,366/yr.
Private foundation funded:
None presently.
Industry Contracts:
None presently

b. Previous Support:
NIH R01HL125042: HIV-induced Redox Stress and the Alveolar Macrophage as a Resistant Reservoir. Funded 7/01/2014-6/30/2018 (Principal Investigator, Multiple PI grant). $686,584/yr; relinquished upon relocation to Cincinnati.
NIH K12 HD072245: Atlanta Pediatric Scholars Program. Funded 04/01/2011-11/30/2016 (Program Director). $324,000/yr.
HHSN275201300003C: Westat/NICHD Contract- IMPAACT Network; Pediatric and Adolescent HIV/AIDS Research Program at Emory University. Funded 9/01/2014-8/31/2019 (Site Principal Investigator). $450,000/yr estimated.
NIAID-DMID-NIH AI2012144: Vaccine and Treatment Evaluation Units (VTEU). Funded 9/13/2013-9/12/2020. (Co-Principal Investigator). $4-5M/yr estimated. 8
NIH R21 AI098592: HIV-specific B cell repertoire in humans following cross-clade immunization. Funded 7/01/2012-6/30/2014 (Principal Investigator). $150,000 initial period; $275,000 direct costs.

NIH R01 AI090656: Broadly-reactive antibodies against chimeric virus-host antigens. Funded 06/14/2010-05/31/2014 (Co-investigator).

I wonder if he knows Ralph Baric??

NIH U01 AI069418: HIV/AIDS Clinical Trials Unit. Funded 2/01/2007-11/30/2013 (Coinvestigator). HHS N272200800005C: Vaccine and Treatment Evaluation Units. Funded 11/01/07- 10/31/14 (Co-Director), $2,494,361/yr.
NIH U01AI78407 : Clonal Analysis of the Human B Cell Response to HIV. Funded 2/01/08-01/31/13 (Co-Investigator), $150,000/yr (Emory component); $750,000 total.
NIH RO1 AI40338: Viral and Cellular Determinants of HIV-1 Assembly. Funded since 1994; (Principal Investigator). $250,000 initial period; $1,150,000 total- now transitioned to GM111027 (active, above).
NIH R01 CA27834: Genetics of Primate “D” Type Retroviruses. Funded 09/24/07- 11/30/12 (Co-investigator), $250,000/yr, $1,250,000 total.
NIH R01 AI084834: Defining Neutralization Breadth in HIV-positive serum. Funded 9/01/2009-8/31/2011 (Principal Investigator), $250,000 initial period, $500,000 total.

NIH R21 AI65312: Pseudovirion Formation by Live Vector HIV Vaccines. Funded 06/01/2006-05/31/2008 (Principal Investigator), $150,000 initial period; $300,000 total.

NIH R01 AI067101: Novel Assays for Inhibitors of HIV Assembly. Funded 6/15/2005- 5/31/2008 (Principal Investigator), $200,000 initial period; $550,000 total.
NIH U01 AI47985: HIV Vaccine Trials Units. Funded 06/00-05/05. $1,438,628 initial period; $7,637,877 total.
NIH P30 AI054999: Vanderbilt-Meharry Developmental CFAR. Funded 05/01/03-04/30- 06 (Co-investigator), $528,468 initial period; $1,633,442 total.
NIH R29 AI40338-01A1: Membrane Binding and Transport of HIV-1 Pr55Gag. Funded 03/97-03/2002 (Principal Investigator). $ 70,000/ year; $350,000 total.
NIH R21 AI44369 (Innovation Grant): Development of Enhanced HIV-1 Pseudovirion Vaccines. Funded 07/99-06/01(Principal Investigator). $140,000/ year; $260,000 total.
NIH R55 CA83527-01A1: Induction of KSHV replication by HIV-1. Funded 03/00-02/02 (Principal Investigator). $80,000 total.
.
.
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NIH R01 AI52007: Development of Enhanced HIV-1 Pseudovirion Vaccines. Funded 06/2002-05/2007 (Principal Investigator), $225,000 initial period, $1,125,000 total.

NAI113678, GlaxoSmithKline: An open-label, multicenter, single arm study to evaluate the safety and tolerability of intravenous zanamavir in the treatment of hospitalized adult, adolescent, and pediatric subjects with confirmed influenza infection. Funded 10/02/12- 05/01/15. Principal Investigator.
P903-23, Cerexa: A multicenter, randomized, observer blinded, activ-controlled study to evaluate the safety, tolerability, efficacy, and pharmacokinetics of ceftaroline vs. comparator in pediatric subjects with acute bacterial skin and skin structure infections. Funded 01/01/2013-12/31/2014. Principal Investigator.
Merck Contract: Protocol 007: A Probe Study of the Safety, Tolerability, and Immunogenicity of a Three-dose Regimen of the Ad5 Gag Vaccine in Healthy Adults. Funded 04/01-12/02, $113,000 total (Principal Investigator).
Merck Contract: Protocol 012: A Probe Study of the Safety, tolerability, and Immunogenicity of the Ad5 HIV-1 Gag Vaccine. Funded 07/01/01-06/30/2003, $114,000 total (Principal Investigator).
Merck Contract: Protocol 016: A phase I dose-ranging study of the safety, tolerability, and immunogenicity of the Merck trivalent adenovirus serotype 5 HIV-1 gag/pol/nef vaccine in a prime-boost regimen in healthy adults. Funded 05/01/03-04/30/05, $117,000 total.
Basic Research Grant, Elizabeth Glaser Pediatric AIDS Foundation: Pseudovirion formation by live vector HIV vaccines. Funded 03/01/02-02/28/2004, $180,000 total.
.
.

LECTURESHIPS, SEMINAR INVITATIONS, AND VISITING PROFESSORSHIPS:
.
.

Invited speaker, Peking University Department of Biomedical Engineering, Beijing, May 2015: “HIV-1 replication in macrophages”
Invited speaker, Chinese Academy of Sciences, Institute of Biophysics, Beijing, May 2015: “Intracellular trafficking of the HIV envelope glycoprotein”

…………

Geeta K. Swamy, M.D.
Expertise: Infectious Diseases

Senior Associate Dean Vice Chair for Research & Faculty Development
Associate Professor, ObGyn
Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine
Duke University, Durham, NC

2004 – 2006 Duke University Associate Faculty Department of Obstetrics & Gynecology Division of Maternal-Fetal Medicine & Division of Clinical & Epidemiological Research

2009 – present Duke University Vaccine Trials Unit Investigator Duke Translational Research Institute Durham, NC

2010 – 2018 Duke University Director Duke Perinatal Research Center Department of Obstetrics & Gynecology Division of Maternal-Fetal Medicine Durham, NC

2012 – present Duke University Associate Professor Department of Obstetrics & Gynecology Division of Maternal-Fetal Medicine & Durham, NC

2013 – present Duke University Human Vaccine Institute Investigator Durham, NC

2016 – 2017 Duke University Associate Dean for Regulatory Oversight & Research Initiatives in Clinical Research Durham, NC

Professional Awards and Special Recognition

2008 NIH Young Investigator Award Perinatal Research Society Meeting, Santa Fe, New Mexico
2010 NIH – NIAID Special Recognition for H1N1 pandemic
2013 and 2014 “Outstanding Reviewer” (Top 10%), Obstetrics and Gynecology
2014 “Outstanding Reviewer” for Vaccine

RESEARCH

Active Grants:
NICHD Maternal-Fetal Medicine Research Units (MFMU) 4/7/11 – 3/31/21

NIH-NICHD (Swamy) Principal Investigator Participation as a clinical site in the NICHD sponsored MFMU Research Network to investigate treatment strategies for common yet unresolved obstetric conditions through large multicenter collaborative trials

Past Grants:
Health Works for Women, NIH Summer Research Fellowship, University of North Carolina at Chapel Hill, Center for Health Promotion & Disease Prevention, 1994

PiiiTCH Study-Prevention of Influenza in Infants by Immunization of Their Household Contacts (CDC, Walter) Co-Investigator

NIH-NIAID (HHSN272200800057C, Swamy) Duke Site Principal Investigator
Randomized, Double-Blind Trial on Safety & Immunogenicity of Inactivated Trivalent Influenza Vaccine in Pregnant Women

NIH-NIAID (HHSN272200800057C, Swamy) Duke Site Principal Investigator A Phase II Study in Pregnant Women to Assess the Safety and Immunogenicity of an Unadjuvanted Sanofi Pasteur H1N1 Inactivated Influenza Vaccine Administered at Two Dose Levels

GlaxoSmithKline (Swamy) Cost-effectiveness of seasonal influenza vaccination during pregnancy An epidemiological study to develop and validate a model for estimating the costs and outcomes related to seasonal influenza vaccination during pregnancy for both mothers and infants through age 6 months.

Charles Hammond Research Fund (Gray) Mentor Assessing Decision Making & Acceptance of H1N1 Influenza Vaccine Administered in a Research Setting In Pregnancy

CDC-NCIRD – 1U01IP000190-01 (Swamy) Principal Investigator Effectiveness of a Vaccination Program in the Community ObGyn Setting The main objective of this 2-year project is to conduct a clinic-based study to develop and assess the effectiveness of a vaccination program for adolescent and adult women in the community Ob/Gyn setting.

ACOG/Merck & Company Research Award on Immunization (Fortner/Swamy) Mentor/Principal Investigator Compliance with Vaccination in the Obstetrical Setting with Novel H1N1 and Seasonal Influenza Retrospective review of births occurring in Durham, North Carolina during the 2009-2010 influenza season to evaluate influenza vaccination practices during the novel H1N1 pandemic.

Charles Hammond Research Fund (Swamy) Principal Investigator Association of Circulating Mitochondrial DNA Content and Preterm Birth Among Black Mothers

NIH-NIAID (HHSN272200800057C, Swamy) Duke Site Principal Investigator A Randomized, Double-Blind Trial on the Safety and Immunogenicity of Seasonal 2010-2011 Inactivated Trivalent Influenza Vaccine in Pregnant Women
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Vaccine & Treatment Evaluation Units 9/16/13 – 9/15/23
NIAID (HHSN272201300017I, Walter and Swamy)
Co- Principal Investigator Participation as a clinical site in the NIAID sponsored VTEU Network to conduct clinical trials of vaccine and treatments for infectious diseases

Contract PI for the following active trials
 A Phase I, Double-Blind, Dose Escalation Study to Evaluate the Safety and Pharmacokinetics of NTM-1632 vs Placebo Administered Intravenously in Healthy Adults

 Group B Streptococcus (GBS) Colonization and Disease Among Pregnant Women: A Historical Cohort Study

 A Phase I Cohort-Randomized, Double-Blind, Controlled Trial in Healthy Adults to Assess the Safety, Reactogenicity, and Immunogenicity of a Monovalent Inactivated Influenza A/H5N8 Virus Vaccine Administered Intramuscularly at Different Dosages Given With or Without AS03 or MF59 Adjuvants: Assessment of Immunological Responses and Lymphocyte Interplay

 A Phase II, Double-Blind, Randomized, Placebo-Controlled, Multicenter Trial to Assess the Safety and Efficacy of 5% Monolaurin Vaginal Gel Administered Intravaginally for the Treatment of Bacterial Vaginosis

 A Double Blind, Randomized, Placebo-Controlled, Phase I Dose Escalation Trial to Evaluate the Safety and Immunogenicity of an Inactivated West Nile Virus Vaccine, Hydro Vax-001, in Healthy Adults

 An Opportunistic Study to Evaluate the Population Pharmacokinetics of Beta-lactam Antibacterials in Adults Including Elderly Subjects (POPS_SILVER)

 A Population Pharmacokinetic Study to Evaluate Disposition of Azithromycin and Ertapenem in Pregnant Women Undergoing Cesarean Delivery After Failed Labor (POPS_CAN_DO)

 Targeted Reduction of Antibiotics Using Procalcitonin in a Multi-center, Randomized, DoubleBlinded, Placebo-Controlled Non-Inferiority Study of Azithromycin Treatment in Outpatient Adults with Suspect Lower Respiratory Tract Infection (LRTI) and a Procalcitonin (PCT) Level of ≤0.25 ng/mL (TRAP-LRTI)

Phase 3, Randomized, Observer-Blind, Placebo-Controlled, Group-Sequential Study to Determine the Immunogenicity and Safety of a RSV F Nanoparticle Vaccine with Aluminum in Healthy 3rd Trimester Pregnant Women; and Safety and Efficacy of Maternally Transferred Antibodies in Preventing RSV Disease in their Infants Novavax, Inc. (Swamy) 12/1/15 – 7/31/19

Principal Investigator Clinical Immunization Safety Assessment (CISA) 9/29/15 – 9/28/18 Clinical Study of the Safety of Simultaneous Administration of Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine (Tdap) and Inactivated Influenza Vaccine (IIV) in Pregnant Women CDC (HHS200-2012-53663, Swamy) Principal Investigator
.
.
.
GlaxoSmithKline Speaker Services, 2009 – 2012

NIH-NIAID Division of Microbiology & Infectious Diseases Working Group on the Enrollment and Safety Assessments of Pregnant Women in Clinical Trials of Drugs and Vaccines, 2010 to 2015

National Vaccine Advisory Committee – Maternal Immunization Working Group – 2014 to 2016

Appointed Member, February 2017 to present
HPV Working Group, February – June 2018

Consultative Workshop on Immunology Research Gaps Related to Maternal Immunization – Bill & Melinda Gates Foundation, May 25-26, 2015

WHO Brighton Collaboration Global Alignment of Immunization Safety Assessment in Pregnancy (GAIA) – Chair, Fetal Distress Working Group – 2015

Independent Data Monitoring Committee, GlaxoSmithKline, Inc. – RSV vaccines for the protection of children, 2015 to 2017

Data Safety Monitoring Board, Randomized Controlled Trial of Influenza Vaccine and Meningococcal Vaccine in Pregnant Malian Women and Their Infants Up To 6 Months of Age, Sponsor: Bill & Melinda Gates Foundation, 2011-2016

………….

Gregg Sylvester, M.D., M.P.H. +
Expertise: Alternate Industry Representative

Vice President – Medical Affairs
Seqirus Inc., Summit, NJ

Physician | Public Health Expert
Pharmaceutical Executive Expert in vaccine preventable diseases, pediatrics and population health.

Career Highlights
• Head of Medical Affairs for Seqirus, a CSL company
• Launched Pfizer’s Pediatric and Adult Pneumococcal conjugate vaccine, as well as Meningococcal B vaccine in the USA
• Launched Merck’s HPV4 vaccine in over 100 countries, presented to numerous National Immunization Technical Advisory Groups (NITAGs), public health and medical societies
• Partnered with community organizations in Delaware to reduce infant mortality, teen pregnancy rates and HIV rates

Professional Experience
SEQIRUS, a CSL company Summit, N.J Vice President, Medical Affairs 2016 – present
• Responsible for the strategy and implementation of Medical Affairs plan
• Ensures appropriate use of Seqirus’ influenza vaccines
• Overseas Phase IV research and presents data to NITAGs and other key stakeholders.

PFIZER VACCINES Collegeville, Pa
Vice President, Medical and Scientific Affairs: Americas 2013 – 2016
• Spearheaded science-based rationale to preserve Prevnar 13 infant schedule in US recommendations
• Successfully achieved an adult Prevnar 13 recommendation from US Advisory Committee on Immunization Practice
• Accelerated launch of groundbreaking Meningococcal B vaccine to accommodate urgent public health need

Global Head of Medical Affairs for Pediatric Vaccines 2010 – 2013
• Global Medical Lead for Pfizer’s Pediatric vaccine, Prevnar 13
• Created medical strategy for Prevnar 13, an asset exceeding over $5 billion in revenue
• Created innovate systems to improved scientific exchanges in a complex, global environment

MERCK VACCINES West Point, PA
Global Head of Medical Affairs for Adolescent Vaccines 2005 – 2010
• Created the medical affairs strategy for Merck’s HPV4 vaccine, Gardasil
• Spokesperson for all Merck vaccines
• Traveled extensively throughout the world presenting to governmental officials, regulatory agencies and public health/medical congresses

CHRISTIANA CARE HEALTH SYSTEM Greenville, DE
Medical Director, Eugene DuPont Preventive Medicine & Rehabilitation Institute 2001 – 2005
• Led Preventive Medicine for Delaware’s largest health care organization
• Expanded the community-based health programs, serving more than 50,000 people/year

DELAWARE HEALTH & SOCIAL SERVICES New Castle, DE
Cabinet Secretary 1997 – 2001
• Reported directly to Governor of the State of Delaware
• Managed the largest state agency, with more than 5,000 employees and an operating budget of ~$1 billion
• Implemented Medicaid Managed Care and Children Health Insurance Program (sCHIP) in Delaware State

Health Officer 1995 – 1997
• Led Delaware’s Public Health Division
• Formulated Public Health policies and supervised programs addressing high infant mortality rates, teen pregnancy rates, and low childhood immunization rates
• Promoted to Cabinet Secretary within one year

Chief of Community Health & Director of Maternal & Child Health 1993 – 1995
• Directed the development and implementation of community-based public health programs for the state of Delaware
• Managed an annual budget of $30,000,000 and 330 public health professionals

Selected Board Positions
IMA World Health: Chairman of the Board: 2017-2018;
Board Member: 2013 – present

DONORS: The majority of IMA World Health’s projects are funded through grants from generous public funding agencies and foundations.
CORUS INTERNATIONAL
◦ IMA World Health | Corus World Health
◦ Lutheran World Relief
◦ CGA Technologies ==> https://www.cgatechnology.com/
◦ Ground Up Investing
◦ LWR Farmers Market Coffee

Selected Honors and Awards
Merck Global Human Health Awards – 2007 & 2006 Winner: Franchise of the Year; 2006 Winner: Best Support of International Markets and 2008, 2007 & 2006

Education & Training Fellowships:

Public Policy – Joseph P. Kennedy, Jr. Foundation, assigned U.S. Senate, Washington, DC
Epidemic Intelligence Service – Centers for Disease Control & Prevention, Atlanta, GA
General Preventive Medicine Resident – Johns Hopkins School of Hygiene and Public Health, Baltimore, MD
Pediatric Intern, Resident and Chief Resident – Children’s Hospital of Buffalo – State University of New York at Buffalo School of Medicine, Buffalo, NY
Master of Public Health – Johns Hopkins School of Hygiene and Public Health, Baltimore,
MD Doctor of Medicine – Albany Medical College, Albany, NY
Bachelor of Arts – (History) – Ithaca College, Ithaca, NY
Veteran Status Commissioned Officer, United States Public Health Service: Rank – Commander – 1990 -1993

Summary

These are the people who have no problem giving an unvetted vaccine to children and pregnant women before the safety data is available. After all, they have been doing it on a smaller scale most of their careers.

-Gail Combs

GC/wm (written/edited)

DEAR KAG: 20220128 – The Pub is OPEN / Wolf’s Big Howl on January Sixth / Defeat The Mandates Picture Gallery / Why Isn’t Vaccine Localization a Thing?

The Pub is OPEN!

It’s GALLERY NIGHT, wherein our intrepid “print screen photographer” and “substitute bartender” presents his “artistic screen shots” of the Defeat The Mandates rally in Washington, DC.

While our beloved REAL bartender takes a needed break of unknown duration, we will continue to ENDEAVOR TO PERSEVERE.

Tonight’s drink special is not ethanol, but rather a different alcohol – epinephrine – a.k.a. – ADRENALINE.

Stay tuned! We’ll explain later!

Christmas Spirit

It looks like SANTA is still somewhere NORTH of the border, but he’s bringing FREEDOM!

Playing on the Jukebox

Well, we were looking for some stuff that was COMPLETELY DIFFERENT on the persnickety jukebox, and look what we found near the end of the last slider…..

EPIC COWBOY/WESTERN ROCK.

What the FREAKIN’ ‘ELL.

https://youtu.be/I8gr2hmIbew

Not sure what’s wrong enough with me to like this, but if you don’t enjoy this crazed version of cowboy, try an even crazier version of “Indian”.

And I mean that BOTH WAYS.

This stuff looks straight out of Burning Man.

And while that’s kind of interesting, it’s not about the kind of FREEDOM that goes with the ART on the wall tonight.

SO – we add some EPIC FREEDOM MOOD MUSIC for your GALLERY TOUR tonight.

That’s more like it.

And now, the rules of the pub.

HOUSE RULES

Now, back to business.

AMEN!

FREE the JANUARY BROTHERS

Article: Another Witness Tells Mafia Nan To GO TO HELL

And in the following video, you can actually hear the HOWL of WOLF MOON, telling MAFIA NAN exactly how he felt, when her Praetorian guard fired GRENADES upon a crowd filled with GRANDPARENTS, WOMEN and CHILDREN on January 6.

https://youtu.be/27Fci99hGww

Source: Capitol Offense: The Ugly Truth Behind The Five Deaths From January 6th and 7th – https://taylerhansen.substack.com/p/capitol-offense-the-ugly-truth-behind

Hat Tip GA/FL who made me aware of this excellent research.

My experience (including my WOLF HOWL) was documented in Section 4 of the following post, entitled

We Are Mighty To Save This Republic

The Truth About Our January Sixth Protest I was there, and I am PROUD of it. I am proud of the thousands and thousands of patriots who showed up to make an historic statement that the other side could only TRY to stop, by besmirching its beauty with their LIES and TRICKERY. Yes, their LIES …

Current Art On The Wall

We have a really interesting PHOTOGRAPHY exhibit in the bar this week. Consider this to be “gallery night”.

Prints are available FREE by right-clicking – or whatever you need to do on your device.

We have more pictures than just this collection, but these are some of the best. Enjoy a selection of magical moments from the DEFEAT THE MANDATES rally in Washington, DC last Sunday.

Dr. Heather Gessling

Dr. Lynn Flynn

Looking for this lady’s name!

Looking for this gal’s name, too!

Ernest Ramirez (vaccine injured and lost son)

And over in the corner, THIS RIGHTEOUS RANT is playing on a loop on our FREEDOM TV.

If you haven’t seen it, watch it. If you have seen it, watch it AGAIN!

Finally, you can watch the entire video HERE:

From: https://thehighwire.com/watch/

And now for our feature presentation…..

Why Isn’t Vaccine Localization a Thing?

One of the thing that tells me science is really out of whack right now, is the fact that scientists are discouraged from doing simple, plain-Jane things that would actually make vaccines safer for the general public, but are instead encouraged to go off in other, riskier, sexier, more profitable directions, while protected by a kind of “media umbrella of propaganda” which justifies, and rationalizes, but does not convince the HONEST skeptic and investigator.

In a sense, we still have the same sort of “patent medicine killers” of the late 19th century, with their poisonous potions – we’ve just changed WHO it is who is allowed to kill people and make money with bad medicines.

The fact that the very first COVID vaccines were of a risky, barely understood, and rather experimental type (mRNA or viral vector, i.e. genetic, full spike, in humans), while EASIER, FASTER, CHEAPER, SAFER, and much more familiar and better-understood vaccine types (protein or glycoprotein antigen, subunit) were IGNORED and SLOW-WALKED until later – well, it would have boggled my mind a long time ago, but no longer.

In my opinion, the “science”, if you can call it that, was guided by FAUCI PATENTS, rather than by what would have been best for patients AND for vaccine science.

The point about damage to vaccine science ITSELF is a point that Robert Malone often makes, which is critical. The people behind the bad, biased, self-interested, money-making vaccine choices, didn’t just screw THE PEOPLE – they screwed up the SCIENCE.

Let me be blunt. When people LIKE ME attack Tony Fauci, we’re not attacking science.

We’re attacking ABUSE OF SCIENCE by an OUT-OF-CONTROL BUREAUCRAT, aided by MERCENARY GLOBAL CORPORATIONS.

Tony Fauci is biased and corrupted by many sick and damaging compromises and ties to the industry he is SUPPOSED to be countering when necessary on America’s behalf – NOT coddling at every personally beneficial turn.

And all of this WRONGNESS was created under the cover of Francis Collins, who was used as a very phony TOTEM of “ethics” and “morality”. The man was pimped to the masses as a great Christian, as if that meant he WOULD and COULD do something about bureaucratic ethics and morality, while those very virtues he was meant to represent but not interfere with, were UNDONE by a series of corrupt administrations.

There is a LOT that is wrong with government regulation of science and medicine right now, and we need to talk about it.

Tonight, I’d like to talk about just ONE point of vaccine science which is weirdly out of whack, and protected ONLY by propaganda – and that is vaccine localization.

That means MAKING THE VACCINE STAY PUT WHERE YOU INJECT IT.

Obviously this is not working. OK? I’ll just be blunt.

One of the points frequently made against actual science on social media, mostly by CCP propagandists, IMO, is that vaccines simply do not leave the injection site, and thus all these systemic and distant effects which people allege to have been caused by vaccines, could not possibly have been caused by the vaccines. I saw this canard far more often than I should have, because people, generally, are not prepared to debate it.

Even when people just argue the evidence back and forth, because the reality is fuzzy and moves around between “localizes” and “migrates”, the argument itself is a fantastic deflection by the “protectors of vaccines”. Instead of talking about the very real problems caused by even LIMITED MIGRATION of vaccines, we’re one step removed from the problems.

These sorts of arguments – that the spike protein vaccines could NOT be migrating from the injection site – were completely undone by the Pfizer data obtained from Japan.

Yes, it was animals, and yes, it was perhaps at an over-sized dose, but the numbers themselves were SO substantial that these kinds of factors basically “factor out”. There is NO DOUBT from this data that there is a RISK of migration of “vaccine which infects cells and cranks out [highly pathogenic] spike protein which is HOPEFULLY dealt with cleanly by the immune system”.

The propaganda that vaccines don’t migrate was CLEARLY violated by the case at hand. That propaganda disappeared rather quickly, although I still hear it from nurses, and just bite my tongue.

Further – shockingly – the idea that the lipid nanoparticles containing the vaccine mRNA (basically what are called “virus-like particles” when injected as part of wasp venom) could actually have time to persist as part of skin lipids and BE SHED – well, it’s rather obvious from the data that this is a very real possibility.

The SKIN is an organ just like everything else. Everything else meaning all the OTHER organs that were getting the vaccine mixed into THEIR lipids in shocking amounts for a very long period of time.

Suddenly the CRAZIEST of the conspiracy theories about the mRNA vaccines was LITERALLY – and I mean LITERALLY – biophysically possible.

I had previously come up with a marginally feasible idea that maybe the spike protein itself was not just toxic, but HORMONE-LEVEL ACTIVE, to explain what people were reporting. But with the Pfizer data, I didn’t need any of that. The VACCINE ITSELF was ready to be shed.

And Pfizer hid this. Yeah. I can kinda see why.

So – if I may – let’s just set aside this foolishness that vaccines don’t migrate, and never have systemic or distant effects, because they do. It’s VARIABLE, but it’s REAL.

So why don’t people DO anything about this?

Why not do things that would absolutely ensure that vaccines CANNOT leave the injection site?

I can imagine a lot of things that MIGHT do this, but had never heard about any adjuvants or additives or vaccine designs that could effectively localize vaccines to arm or shoulder muscle, and simply make sure they didn’t migrate to even the slightest degree.

Solve THAT problem and pericarditis is GONE – RIGHT?

So why not do it? And why not BRAG about it if you CAN do it? Why not say how it’s done?

CRICKETS.

FAST FORWARD to a recent bit of knowledge that I happened upon IN REAL LIFE.

I noticed that I was somewhat jittery after having some minor dental work done. I was quite numb for the work, but later, after leaving the dentist’s office, with the numbness now faded, I noticed that I was shaky, edgy, and “wired”. That went away over the rest of the day. I just assumed that it was a side effect of the anesthetic.

I mentioned this to an anesthesiologist and a nurse, who both explained to me that it was NOT due to the anesthetic, but rather to epinephrine, which is sometimes ADDED to an injectable anesthetic in order to LOCALIZE it.

They explained to me that by epinephrine constricting the blood vessels in the region where the anesthetic is injected, the body removes less of the anesthetic by drawing it away in the blood stream – so the anesthetic STAYS at the site of the injection, giving a longer duration of anesthesia.

Sure enough, when I looked this up online, I found out it is quite real.

**https://journals.lww.com/anesthesia-analgesia/Fulltext/1998/05000/The_Effect_of_Varied_Doses_of_Epinephrine_on.21.aspx**

So I immediately thought to myself – why not do the same thing with vaccines?

Why not try to localize them with something like epinephrine?

But when I looked THAT up, the only results that I got, were for use of epinephrine (you know, as in the EPI PEN) in treating anaphylactic reactions TO vaccines. I probably didn’t look hard enough, but I’m not trying to get a patent or anything like that.

So who knows? It may be that adding epinephrine to vaccines could actually be GOOD in terms of reducing the severity of anaphylactic reactions – in addition to localizing the vaccine.

However, the possible technical feasibility of doing something isn’t my point.

My main point is simply ADMITTING THERE IS A PROBLEM.

If you could simply make these DAMN mRNA vaccines STAY where you put them, and if they didn’t crank out a bunch of bad stuff into the blood stream, then perhaps the only long-term risk would be something like cancer AT THE SITE OF INJECTION.

However, let’s be real. Nobody even TALKS about the problem. The media just DENIES IT.

In my opinion, “they” aren’t addressing this problem, because it gets on the way of “their” real purpose or purposes.

Vaccine localization is the last thing that these people wanted to “solve” here.

The people who CONTROL science and medicine don’t have to tell us about their entire agenda. They only have to tell us things that are somewhat plausible and rational.

In my opinion, mandatory vaccination is a PLATFORM for SOCIALISTS to do whatever they want to whomever they want. It gives them cart blanche to change society without accountability. That is the big picture, and has been their objective for well over 100 years.

Look at what communists are doing to Uighurs in Communist China RIGHT NOW.

Former #Uyghur camp detainees said they were given injections that stopped their periods or caused unusual bleeding consistent with the effects of birth-control drugs. #China_kills_muslims #EVilCCP https://t.co/xSDOvxS6xL
— Jeshurum david (@DavidJeshurum) July 17, 2020

Of Course: Bill Gates Praises China’s Response to COVID https://t.co/meIzorcKSM
— Sharon (@SweetFreedom29) January 24, 2022

Changing PEOPLE directly changes society FASTER.

They want to keep you alive, they keep you alive.
They want to sterilize you, they sterilize you.
They want to experiment on you, they experiment on you.
They want to kill you, they kill you.

Doing things which do not contribute to, or which would actually IMPEDE their “unholy grail” goal of direct control over humans, is simply NOT going to happen, if THEY can help it.

But that doesn’t mean that WE can’t give them a BAD HAIR DAY, EVERY SINGLE DAY, and fight for WHAT IS RIGHT in science and medicine.

defederalization of science
destalinization of medicine (de-obamatization in practice)
force ethics and transparency where socialists don’t want them
bring anti-deception tools and language INTO science itself
chase politics out of science, acting in both of them
increase citizen science literacy outside compromised institutions
work toward a BOR-compatible medical freedom amendment
many more

SO – just remember this.

Science and medicine won’t change when THEY do something about it.

Science and medicine will change when WE do something about it.

ENJOY THE SHOW.

W

WE HAVE THE COOKIES!

7136ad67c6068a95c5577c9397afad2b

DEAR KAG: 20220107 – The Pub is OPEN / TES Special Edition / Pimp Your Coof Kit / Dealing With Uncertainty / ThEthSkep’s Big Fix of All Things Coof: CCP Hiding Chinese 2018 Release of SARS-CoV-2 Virus

The Pub is OPEN!

Yeah, we still have staffing problems, but who doesn’t under China Joe?

While off to a rocky start, we are staying open as many days of the week as possible, just like some of the small businesses that I patronize.

Keep up that LOCAL PRESSURE on the Biden cabal by going to school board meetings and supporting TRUE non-monopoly capitalism – it SKEERS Kapo and Little Red Jen somethin’ FIERCE.

Merry Christmas and Happy Holidays! To the White House press– thank you for challenging us, for questioning and for holding us accountable as we all work to keep the American people informed. And to the press team–you are simply the best. Grateful every day to work with you. pic.twitter.com/xxBwLMzh2L
— Karine Jean-Pierre Archived (@PressSec46) December 23, 2021

Likewise, patronize those SMALL BLOGS that provide new viewpoints and ideas!

We Serve Whiskey And Guns To Indians Here!

Yup! FREEDOM is GOOD TROUBLE, and we’re in favor of it, for everybody, much to the consternation of our local maskies and vaxxies.

I had the special pleasure of being “refused service” by a maskie recently – he simply walked away from the cash register and went into the back. Some of it was due to race. Having been “not served” because of race before, I can spot that fairly easily, and this person was not exactly “hard to read”.

Three other staffers (all forced to wear masks, sadly) came to my assistance and took my order.

I maintained a pleasant demeanor, as part of one of several psychological warfare tactics that I have adopted recently, in fighting against the VAXZIS and MASKZIS.

While our beloved REAL bartender takes a needed break of unknown duration, we continue to ENDEAVOR TO PERSEVERE.

So what’s on the ODD BAR’S CRAZY MENU this week?

We’ve served alcohols our first week, including menthol, ivermectin, and hydroxychloroquine.

Next, we served amines , including second generation antihistamines.

Today, we’ll toast each other with an element that we’ll borrow from Steve…..

…..and some very special natural alcohols and derivatives, including among the 4 of them, 3 terpenoids, 2 phenols, 1 ester, and 1 ether.

More on these wonderful “liqueurs” later!

Christmas Spirit

There’s still time to spread omicron! GET BUSY!!!

While we do have some members out with Omicron now, including Brave and Free, the real question is whether we’re going to see a big peak in March and April, like we did in 2020.

And if you’re gonna get sick, you might at least consider having some willing cohort, looking for that natural immunity, to get sick with you!

thank you pictures

Ah, thanks to SMILEY for reminding me of the goofy fun of these wonderful but stupid GIFs called “Blingees”!

And now, the rules of the pub.

HOUSE RULES

Now, back to business.

AMEN!

Current Art On The Wall

Now for something a bit different…..

Vector background. Molecules and chemical formulas

…..and something a bit more familiar.

David Teniers the Younger (1610–1690), *The Alchemist*, ca. 1643–45. Oil on panel, 20 1/8 x 28 in (51 x 71 cm). Herzog Anton Ulrich Museum, Braunschweig (139)

LINK: https://www.metmuseum.org/blogs/now-at-the-met/2020/alchemy-science-making-marvels

TES Special Edition

As one of the early “discoverers” of The Ethical Skeptic on Twitter, I was happy that I was able to get a few people interested in his precise and well-considered thoughts on things – especially regarding the phony scamdemic. TES was always utterly perturbed by the bad science of the “pandemic”, and worked on a daily basis to “correct the fact checkers” – which was all of hilarious, sad, and joyful.

After I was kicked off Twitter, I rarely saw him, due to my own laziness, really, but in 2021, some GREAT links to The Ethical Skeptic’s work popped up here. THANK YOU, to all who follow him and keep us informed.

THIS was a classic.

LINK: https://theethicalskeptic.com/2019/03/07/nelsonian-inference-and-cultivated-ignorance/

ARCHIVE: https://archive.fo/wZKYb

This work really helped me to GRASP and understand the leftist tactic of “pretending not to know”, and – more importantly – how to spot it.

So let’s look at some of his even more recent stuff.

Pimp Your Coof Kit

LINK: https://theethicalskeptic.com/2021/12/29/our-household-covid-kit-item-listing/

This one got us all thinking about “coof kits”, and GA/FL suggested some of us putting up our own versions. I initially thought that this might not be a good idea, because people’s needs and medical situations really VARY – one of the main reasons that “practicing medicine without a license” is actually a bad idea in normal times. I thought it better to have a broader discussion.

However, I just realized that I did put up a kind of “minimal” kit last week, and it’s worth looking at it.

This kit was designed for people who DON’T have a smart plan already figured out, and don’t want to investigate “hard to find” things like ivermectin and hydroxychloroquine.

Here is what I had, followed by my earlier reasoning. The main change is adding Vitamin C, as discussed below.

Wolf’s COVID Care Package

Thermometer (thermal digital is easiest)
Antigen test kit(s) (yeah, good luck finding one, although they are coming back after New Years)
Antihistamine of your choice (Claritin, Zyrtec, and Allegra are the easiest – 1-2 a day)
Aspirin (regular, or low-dose if your stomach doesn’t like it – 1 a day)
Listerine or Betadine mouthwash/gargle for mouth and throat
Vitamins C and D, Zinc, Calcium, Magnesium, Multivitamin including Selenium.
Quercetin (including natural sources) or Green Tea
Saline or other nasal spray, rinse, or wash of your choice

The thermometer tells you when to use your precious test kit – when you suddenly have a fever and a sore or tingly throat.

The test kit gets you a positive diagnosis that opens doors for things like antibodies, or an official test.

A positive test means you can BEGIN TREATMENT at THERAPEUTIC DOSES.

The antihistamine insures that YOU WILL ALMOST CERTAINLY NOT DIE, because it stops the second, allergic, inflammatory stage of COVID in its tracks.

The aspirin makes doubly sure you won’t get clots, but be careful – don’t take it if you’ve had trouble with aspirin. Talk to your doctor if unsure.

The gargles (Listerine or Betadine) massively reduce viral load and speed time to recovery.

The saline and nasal washes lower viral load, and maintain nasal breathing.

The quercetin and green tea help zinc’s antiviral action by increasing cellular zinc levels.

The vitamins and mineral supplements keep you at antiviral levels of these things. In particular, zinc and vitamin D3 need to be at non-deficient levels.

Please consult authoritative sources from TRUE medical doctors like the ones at https://flccc.net.

Cthulhu noted that I hadn’t mentioned Vitamin C – I have now added that, because it’s likely to help and can’t hurt (“First, do no harm”) and also follows the McCullough Principle (“Signals of Benefit, Acceptable Safety”). I don’t think it’s nearly as important as the antihistamine and “clot-blocker”, but I do have to admit that Vitamin C was certainly far better than nothing when I survived Wuhan with only mild lung damage.

What I’m going to do now is to encourage all of YOU to talk about your “war chests” and “coof kits”, and explain your reasonings about things.

This will help people who are deciding what THEY might want to add to their kits – OR REMOVE, if there is something better for their particular situation.

Remember – everybody has their own unique medical needs.

I will put my thoughts in the comments, just like everybody else.

NOW – about those natural “essential oils” in Listerine.

Let’s look at them.

Menthol

Thymol

Eucalyptol (2 views)

Methyl salicylate

These are all natural substances of roughly the same molecular size and composition (mostly carbon and hydrogen with 1-3 oxygen atoms), all of them being either pungent oily liquids or smelly, vaporous crystalline solids.

There are some relations between these things.

Thymol is basically menthol where the 6-membered ring has been made benzenoid – meaning like benzene – with 3 double bonds.

Notice that methyl salicylate is also benzenoid. Methyl salicylate is related to aspirin, and has similar activities. Don’t drink Listerine, even though the amounts are (believe it or not) rather small.

Eucalyptol is also structurally related to menthol, although it’s harder to see. Try to see it.

All of these natural substances, when isolated from their sources, were very early pharmaceuticals. They ALL have pharmacological activities, which many would regard as “primitive” by today’s standards, and yet, gargling Listerine is PROVEN to be extremely effective in reducing viral load of COVID-19 variants – about 80% as effective as iodine solutions.

Why might this be? Here is just ONE small line of immunological evidence.

LINK: https://pubmed.ncbi.nlm.nih.gov/9810029/

To be honest, we’re a bit late to the game here. Native Australians from the first wave of immigration, roughly 65,000 years ago, discovered the utility of eucalyptol by their own investigations.

LINK: https://successfulaffiliateru.com/medicinal-use-of-eucalyptus-the-australian-aboriginal-way/

Here is some additional information about early Australian medicine using natural products.

LINK: https://theconversation.com/the-art-of-healing-five-medicinal-plants-used-by-aboriginal-australians-97249

There is a great picture of what is essentially a native doctor’s medical bag in the second link. When it freaks you out a bit, let it. This is a way of getting you to appreciate human intelligence outside your modern experience.

Lastly – IODINE.

I have not tried this, and I am not sure I would like it, but it’s a viable option, IMO. I actually like Listerine, and it worked for me on delta, so I’m happy with that. I did NOT try Listerine in the nasal cavity. Not sure that I’d like that. I stuck to saline.

I did find a paper that showed Listerine to be roughly 80% as effective as povidone-iodine.

Here is link to a review which states something similar, and a summary of the review.

LINK: https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC7842245/

Executive summary

Methods

A review of literature was conducted regarding the use of commercially available antiseptics and SARS-CoV-2.

Results

Povidone-iodine (betadine), ethanol and essential oils (Listerine) and a combination of xylitol and iota-carrageenan (purified from red marine algae) were shown to reduce viral load of SARS-CoV-2 in vitro by 3–4 log₁₀ in 30 s.
Chlorhexidine, a widely used oral rinse, does not act as quickly in reducing viral load in 30 s as povidone-iodineI, but binds to cell proteins, extending protection.
Hydrogen peroxide is not as effective as other oral rinses in vitro and cell toxicity is a concern.
Hypertonic saline is not directly virucidal, but halts replication by increasing hypochlorous acid inside the cell.

Conclusion

Several commonly used nasal antiseptics and gargles have shown efficacy against SARS-CoV-2 in vitro and clinical trials are currently underway to study their impact on disease course and transmission.

Future perspective

These commercially available products should be further evaluated due to their potential ability to reduce the transmission of SARS-CoV-2 and other viruses that are yet to emerge.

You can also make your own povidone-iodine gargles and nasal rinses – Dr. McCullough has retweeted a nice recipe for this. Click through to Twitter for more information.

pic.twitter.com/JfPLaJgHAd
— Joel "Heart Prevention" Kahn MD, FACC (@drjkahn) December 31, 2021

Here is a great long post on all of these methods, including hydrogen peroxide – an alternative to iodine.

LINK: https://jeffreydachmd.com/2021/09/povidone-iodine-mouth-wash-rinse-gargle-for-c0-ld-prevention/

Do beware that some people need to be careful with iodine, including people with hypothyroid.

LINK: https://www.webmd.com/diet/foods-high-in-iodine#1

LINK: https://www.webmd.com/vitamins/ai/ingredientmono-35/iodine

Dealing With Uncertainty

LINK: https://theethicalskeptic.com/2021/12/24/the-riddle-of-certainty/

ARCHIVE: https://archive.ph/wpfWu

This is another GREAT article, talking about one of my FAVORITE complaints about modern science, which has resulted from a really SICK and UNHEALTHY compartmentalization, as well as insulation of scientists from internal criticism (lack of “herd review”). This condition has allowed all sorts of pathological science to gain ascendancy without check, balance, or proper community criticism.

For example, CLIMATE CHANGE gets more input from FINANCIERS than it does from the many scientists like me who think we are acting irrationally and presumptuously on ERRORS. These errors have been induced by the WRONG forces – beneficiaries not committed to truth – within a small pathologically influenced community – much like what’s going on with improperly influenced government science and the “clot shot”.

This piece by The Ethical Skeptic contains a graphic using a BULLSEYE which you really need to see. It makes a very important point about science – which I can apply DIRECTLY to Anthony Fauci.

Fauci’s extreme focus on antibodies to the spike protein as a nearly sole measure of “success” of the “clot shot”, is a perfect example of what TES is talking about.

I have referred to Fauci’s over-focus as “antibody hypnosis”. In fact, I see this kind of obsession and compulsion repeatedly throughout his career, and would wager that:

it’s why he always “wins” against the Judy Mikovitses and the Kary Mullises
it’s why he’s so highly paid
it’s why he’s tied to so many “grim reaper” experiments
it’s why corrupt industry loves him, and is in bed with him

TES makes a general point about the kinds of information which actually provide STRONGER PROOF – and this set includes something I love – INDEPENDENT CONFIRMATION BY ALTERNATE LINES OF REASONING – not just “duplication of results” and “confirmation of results” – which are both sadly lacking as well, but not nearly as important.

I have powerful, direct experiences in science with the need for RESOLVED DIVERSE INPUTS and AVOIDANCE OF HYPNOTIC REASONING as safeguards against pathological science.

However, THEY (and I mean “they”) are using various forms of hypnosis, including MASS, COMMUNITY, PEER, and INDIVIDUAL to advance science in ways that THEY want.

Human science is far more controlled than we either admit or understand.

Anyway, back to the article.

There is a quote from Elon Musk therein which is really worth your while, and which TES puts in the context of what he is talking about.

Bluntly, it feels wonderful to know that SOMEBODY GETS IT.

What Musk is talking about here is basically the “bullseye” metaphor that TES uses. And THAT is related to the following item.

While Fauci is very committed to the LEVELS of his antibodies, he has not properly processed feedback that would indicate he’s OPTIMIZING THE WRONG THING.

Here is a link to Steve Kirsch’s interpretation of Sucharit Bhakdi’s and Arne Burkhardt’s analysis of people who died after vaccination, showing that these deaths were ALMOST ALL related to the “clot shot”.

LINK: https://stevekirsch.substack.com/p/bhakdiburkhardt-pathology-results

Kirsch REALLY explains this well. Malone takes note of this, too.

IMO, it would appear that Fauci is optimizing the WRONG ANTIBODIES in the WRONG WAY, because the vaccines are CREATING the WRONG ANTIBODIES in the WRONG PLACES.

Please read Kirsch’s article and then the Bhakdi-Burkhardt paper to understand this.

PAPER: https://doctors4covidethics.org/wp-content/uploads/2021/12/end-covax.pdf

Now, Fauci may be optimizing the wrong antibodies in the wrong places for a variety of reasons. Those exact reasons are not nearly as important as the fact that they are simply WRONG.

I believe Bhakdi, Burkhardt, and Kirsch – this is a risky vaccine, and now we begin to understand WHY.

Based on this knowledge, I personally will not be taking these vaccines.

In my opinion, these results CLEARLY show that vaccination against SARS-CoV-2 should not be effected by IM injections of a full SARS-CoV-2 spike protein, and even more emphatically so, NOT by genetic vaccines delivered by IM injections. In my very early opinion, this is going to be a CLASSIC case for using RBD antigen (protein) and/or nasal delivery as a concession to the virus – with nasal delivery being used as a SAFETY feature and NOT merely a convenience.

To have SAFER vaccines for DISCRIMINATING SHOPPERS like me, we’re going to have to compromise with the virus. That’s just the way it is.

There may be SOME who thought that we could arrive at a compromise that would reduce human populations, but frankly I don’t like that deal.

In my opinion, ANYBODY with vascular, cardiac, clotting, or other issues like WANTING TO HAVE KIDS SOMEDAY, or NOT RISKING CANCER, should absolutely avoid the current clot shots.

In my opinion, the clot shot is stupidity advanced by greedy people who are controlled and manipulated by really evil people. In other words, it’s not stupid, greedy, or evil – it’s ALL OF THE ABOVE.

The DISEASE is no picnic, and I can see some people making the risk-benefit calculation in favor of the vaccine – particularly newer RBD antigen vaccines like Corbevax (Hotez/Baylor/India/open-source). But if people are dying in 5 years from experimental mRNA vaccines with the full spike protein – well, that is exactly like the RISK that one takes with SMOKING SOMETHING YOU DON’T UNDERSTAND.

Seriously, most Americans would refuse to take a novel “legal” or illegal designer drug, given stories like the “bath salts” and “Parkinson’s heroin” experiences which shocked the public in horror headlines.

Parkinson’s from Designer Heroin (Ironically related to Paraquat)

LINK: https://www.latimes.com/archives/la-xpm-1985-07-29-me-5136-story.html

LINK: https://pubmed.ncbi.nlm.nih.gov/28282815/

VIDEOS: https://duckduckgo.com/?q=mptp&iax=videos&ia=videos (warning – they’re really sad)

Effects of “Bath Salts” (Euphemism for CCP Designer Drugs)

LINK: https://www.npr.org/sections/parallels/2014/06/16/321779232/how-bath-salts-a-drug-made-in-china-wreaked-havoc-in-the-u-s

LINK: https://www.justice.gov/usao-wdny/pr/akron-man-arrested-importing-bath-salts-china

The CLOT SHOT is a RISK, and not all of us will want to take that risk.

Mandating that risk is EVIL, IMO, and Democrats deserve to DIE AT THE POLLS in November for it.

Period.

They have BLOOD on their hands.

ThEthSkep’s Big Fix of All Things Coof

LINK: https://theethicalskeptic.com/2021/11/15/chinas-ccp-concealed-sars-cov-2-presence-in-china-as-far-back-as-march-2018/

ARCHIVE: https://archive.fo/zww1q

This is what I really wanted to show you, right here.

The Ethical Skeptic, or TES, or “ThEthSkep“, as I sometimes call him, has proven to my satisfaction that CCP lied even MORE than we previously thought possible.

Is this hard to believe? That we got CHUMPED by CHINA yet again?

Yeah. Getting chumped by China YET AGAIN is a thing.

I am tempted to try to construct an “elevator pitch” of ThEthSkep’s argument, and have even asked him (in a moderated comment) if he could provide such a short explanation that I could pitch to others.

If he DOES provide one, I will do an entire post on it.

For the moment, I will just give you my “two paragraph description” of his very long and elegant post, which post I can guarantee most here will have trouble following.

TES argues that setting an earlier date for the actual initial Chinese release of an ancestral pathogen to current SARS-CoV-2, provides a far better explanation of the facts at hand, as well as some facts which he generated through analysis of the genetics of SARS-CoV-2 variants, than does the “standard model” of a late 2019 release, whether that late release is taken from the early Chinese LIES about a zoonotic outbreak in December 2019, or from the October 2019 Wuhan lab activities which have always struck me as potential disinformation.

In particular, an early 2018 release of a less pathogenic ancestor explains the omicron variant’s surprisingly early 2020 appearance and low pathogenicity so well, and China’s population resistance to the more pathogenic Wuhan variant, whether that was a descendant or (my thinking) a new release, that IMO it is the duty of the “standard model” to explain all of the facts better than the TES theory.

Now, like I said, this post by TES is not an easy read, even for those with some knowledge of the field, and even for those experienced in reading the scientific literature. He moves at “review speed” through a lot of reasoning and even his own work, which is not all shown, but which is all fully described and referenced.

I am actually WAITING for my first reading to fully sink in, but I can tell you this. As soon as I “freed myself” from the necessity of a late 2019 release, everything “coof” just started falling into place.

This is one of those things that starts generating RESETS in my mind, on everything I had thought before. Once you see what TES is getting at, it’s almost impossible to unsee it.

AND I CAN GO FURTHER.

I talk to a LOT of people, and listen carefully to their thinking about COVID. One of my sources is somebody who has a lot of contacts in Europe and Asia, especially India, due to working for an international firm.

That person strongly believes, based on illnesses within the corporation as well as associated entities, that something like COVID-19 was already circulating worldwide during ALL of 2019.

I had set this aside, unable to fit it into everything else I knew. NOW, however, it makes easy sense. In fact, the details which I don’t want to give, fit his model of spread EXACTLY.

If TES is correct, and I believe he is, then WE WERE DEALING WITH VARIANTS EVEN BEFORE THE CDC BEGAN TALKING ABOUT VARIANTS. In fact, they never told us that THE ORIGINAL WAS LIKELY JUST A VARIANT OF SOME PRIOR VARIANT.

And THIS explains much better why Fauci, Baric, Dazsak, and all the others were ready to cover up – because a virus related to their research had already gotten out in 2018. Going along with the Chinese story was a RELIEF to them – and they grabbed on tightly.

In other words, a conspiracy of aligning interests, not something discussed on paper or by phone. It’s a brilliant Chinese move, actually. Proffer a lie and see if our own scientists will join them in it.

The USEFUL IDIOT American media? NO PROBLEM.

And not just THAT stuff, but now we have much more evidence that these bugs could have been “in the wild” EVERYWHERE – including possibly just outside the Baric lab, near where Gail Combs picked up a “coofy” bug much earlier than would have been possible with a late 2019 release. (I will let her address the time-frames.)

Consider that China could even have been trying to FRAME or intimidate Baric with a stateside release in the vicinity of his lab. Why? Because NOW we have MOTIVE.

Does it make sense NOW that these highly contagious bugs could have been getting out willy-nilly from these laboratories? Or that China has been playing fast and loose with biological releases?

What does this mean?

It means that the whole NIH-Fauci-Wuhan complex has been in cover-up mode, trying to SAVE THEIR DANGEROUS RESEARCH which they know is VERY likely to be SHUT DOWN BY A CONGRESS RUN BY THE PEOPLE – no matter WHAT THE CAUSE OF THIS RELEASE.

Remember how I said the President Wolf Moon would send a cruise missile into every BSL level 4 that didn’t shut down immediately upon his inauguration? Those missiles armed with whatever insured that all viruses were FRIED?

See the motive to get rid of Trump now? WE THE PEOPLE cannot be allowed to interfere with their “holy” research.

And wait – there’s MOAR.

Somewhere in the years between 2005 and 2010, around the time I got an extremely SARS-CoV-2-like infection, complete with anosmia, exhaustion, and “sore lung”, I took note of the fact that all of my Asian colleagues in the “anti-CCP” camp became very religious about taking COVID-like precautions in our CCP-Chinese-infested workplace. These precautions included isolation, surface and aerosol measures, like wipes, air filters, and even clothing choices.

Most of us dismissed it as an “Asian thing” like masks, even though it was a sudden and new social phenomenon, but because I had contacts in that community who were sometimes sources of insight on CCP skulduggery, I noticed that ONLY the “antis” were engaging in the protective behaviors – the mainlanders and pro-CCP Hong Kongers/Taiwanese were not.

Interestingly, I was not getting any good information on the trend – unlike other scuttlebutt at the time.

Was it real or disinformation? Was it an op to flush out the antis? Was it “anti” paranoia?

I have no idea. But I personally think that China has been up to “bio-tricks” for a LONG time – as in back BEFORE SARS (2003).

If 2018 is the first time China released any biologicals, I would be VERY surprised.

SO – see what you think. Read this sucker, and then think about it.

I think TES is onto something.

A Note About January 6 – and More

I have been avoiding all things January 6, largely because I don’t want to give Nancy Gambino any “lift” as far as her phony “investigation” into HER OWN CRIME.

I understand her game plan, and I’m not going to play along.

I would have loved to have recounted that amazing day in another long, glowing, “all about me and my experiences” post, but no.

THIS IS WAR.

In my opinion, we can bring down these horrible communists faster by focusing on whatever WE want to focus on.

Nancy says “the fight is over here”.

NOPE. Go to hell, Mafia Bitch. We know what you did. With Kapo’s dirty FBI. And the backing of Mitch McConnell and SCOFFLAW SCOTUS.

Some may want to join the fight against Pelosi right now, and please feel free to “follow Darren Beattie into Pelosi’s breach”, but I think that MANDATES are going to kill these bastards at the polls, if we just help them commit electoral suicide.

Expose the “clot shot” risks more fully, and show that the mandates are MORE EVIL.

We need to make Democrats – destroying America for GREED under the cover of virtue signals – absolutely unelectable, and I think we can.

ENJOY THE SHOW.

Thank you all for being here. Have a great weekend.