The Nuremberg Code vs US Law and The Push For World Government

TradeBait2 Made the comment:

I have been reminding folks on here – the Fed has to be bankrupted at some point. It will either be by the white hats or the black hats. The Gab post you show is correct for the most part IMO. The Fed has fueled the Great Reset, which is why they could care less about how much debt we have in America because we will not exist as an independent nation in their black hat world.
Digital one world currency is the plan. Why do you think there were coin shortages recently? Why do you think they hate crypto and parallel economies so much? Why do they want America at odds with Russia, but falling right in line with China? Where Xi falls in this I am not certain. But I do know China and the Chi-coms are a CB [central bank] creation.
The linchpin is digital currency.
Follow the money….

That is the first half of the comment

Actually I can see where he is going since I also have warned of this much earlier.

The Push For World Government

A few years ago Soros directed the USA to overthrow the ELECTED government in both Syria and Ukraine. (Trump side stepped both.)

Why? Because the EU is the model for a global government. Soros wanted the EU to annex the Ukraine. The elected president said HE!! NO! so he was ousted and a pro-EU puppet was put in his place who has since been voted out while Trump was in the White House.

Russia tossed Soros out and put out a warrant for him. Russia makes much of their money selling gas to Europe. It also gives them leverage to keep the EU from expanding into their sphere of influence. Soros wants to remove Russia’s leverage by putting in a pipeline from the middle east to Europe. ALL the countries that were opposed to that pipeline have been overthrown EXCEPT for Syria.

If you want a World Government similar to the European Union then you are on Soros side. If you want sovereign nations you are on the side of Russia….. AND I am still of that opinion.

BREXIT THE MOVIE will give you the details on how the EU is actually run.

https://www.youtube.com/watch?v=UTMxfAkxfQ0

Former World Trade Organization Director-General Pascal Lamy tells you point blank that the EU is the template for the desired World Government and it has been the plan since the 1930s.

All had lived through the chaos of the 1930s — when turning inwards led to economic depression, nationalism and war. All, including the defeated powers, agreed that the road to peace lay with building a new international order — and an approach to international relations that questioned the Westphalian, sacrosanct principle of sovereignty…
Pascal Lamy, Whither Globalization

Lamy is quite blunt in stating national sovereignty is passé:

…more than half a century ago that the Frenchman Jean Monnet, one of the shapers of post-war Europe, said, “The sovereign nations of the past can no longer provide a framework for the resolution of our present problems. And the European Community itself is no more than a step towards the organizational forms of tomorrow’s world.” His assessment was as valid then as it is now….
Pascal Lamy, Global Governance: Lessons from Europe

Lamy indicates that a super state fashioned after the European Union is the goal and he calls for European-Inspired Global Governance:

This is what Global Warming was really about. We have all seen the political message morph over the decades from Global Warming to Climate Change to Weather Weirding.

As H.L. Mencken said:

“The whole aim of practical politics is to keep the populace alarmed — and hence clamorous to be led to safety — by menacing it with an endless series of hobgoblins, all of them imaginary.”

In other words, create a crisis to order to implement Diocletian’s Problem-Reaction-Solution

Mencken also warns:

“The urge to save humanity is almost always only a false face for the urge to rule it.”

The UN put the concept into practice via the IPCC. The IPCC mandate states:

The Intergovernmental Panel on Climate Change (IPCC) was established by the United Nations Environmental Programme (UNEP) and the World Meteorological Organization (WMO) in 1988 to assess the scientific, technical and socio-economic information relevant for the understanding of human induced climate change, its potential impacts and options for mitigation and adaptation. http//www.ipcc-wg2.gov/ (No longer available)
IPCC

Notice the IPCC ASSUMES the hypothesis of human induced climate change IS TRUE and goes from there.

With Reagan killing off the Cold War, Pascal Lamy takes ‘Practical Politics’ the next step, by telling us about a “new enemy to unite us” (Global Warming) A global enemy needed to create Legitimacy, one of the ‘four legs’ needed to implement a global government…

I see four main challenges for global governance today.
The first one is leadership, i.e. the capacity to embody a vision and inspire action, in order to create momentum. Who is the leader? Should it be a superpower? A group of national leaders? Selected by whom? Or should it be an international organization?
The second one is efficiency, i.e. the capacity to mobilize resources, to solve the problems in the international sphere, to bring about concrete and visible results for the benefit of the people. The main challenge here is that the Westphalian order gives a premium to “naysayers” who can block decisions, thereby impeding results. The ensuing viscosity of international decision-making puts into question the efficiency of the international system.
The third one is coherence, for the international system is based on specialization. Each international organization focuses on a limited number of issues. The World Trade Organisation deals with trade, the International Labour Organisation with labour issues, the World Meteorological Organisation with meteorology and so the list continues. It is a fact: the UN is not really overarching, assuming this was the initial intention.
The last challenge that I see is that of legitimacy— for legitimacy is intrinsically linked to proximity, to a sense of “togetherness”. By togetherness, I mean the shared feeling of belonging to a community. This feeling, which is generally strong at the local level, tends to weaken significantly as distance to power systems grows. It finds its roots in common myths, a common history, and a collective cultural heritage. It is no surprise that taxation and redistribution policies remain mostly local!
There is one place where attempts to deal with these challenges have been made and where new forms of governance have been tested for the last 60 years: in Europe. The European construction is the most ambitious experiment in supranational governance ever attempted up to now. It is the story of a desired, delineated and organized interdependence between its Member States…. http://www.wto.org/english/news_e/sppl_e/sppl220_e.htm
Pascal Lamy

In another presentation Lamy again addresses the problem of legitimacy:

It gives me great pleasure to be here today to participate in this thematic debate on the United Nations in global governance, an issue of the utmost importance given the urgency of the global challenges we are facing… As for legitimacy, I see two avenues to strengthen it. First, domestically, by increasing the visibility of international issues and giving citizens a greater say…. https://archive.globalpolicy.org/social-and-economic-policy/the-three-sisters-and-other-institutions/global-governance-and-the-three-sisters-1-11/50398-lamy-urges-raising-un-ecosoc-profile.html%3Fitemid=id.html
Pascal Lamy

By now, with Al Gore exiting stage left, Trump entering stage right, it is pretty obvious that ‘Global Warming’ has lost its high panic factor and the climb down is in progress. However the need for a ‘Crisis to Unite Us’ and a reason to implement ‘Agenda 21 – Sustainability’ and ‘Global Governance’ still remains. WORSE for the Globalists the fiat currency central banking system is on its last legs and about to IMPLODE, as many people like Dave of the X22 Report and Clif High and others have been warning us. Up to now we have been wondering what the next hobgoblin would be. And now we know it’s COVID -19!!! A Bio-Weapon and a Poison Jab that kills off a lot of the population, crashes the world economy and ushers in a Vaccine Digital Passport soon to be linked to the BRAND NEW DIGITAL WORLD CURRENCY and Social Credit Score.

And that brings us to the second part of TradeBait2’s comment.

…… You do not want to use the Nuremberg Code as your get out jail free card from jabs. You fall into the hands of international law superseding national law. It’s a set up, don’t fall for it.
Cannot tell you the number of times I have prepared a post and deleted it because I doubted folks on here would pay attention or believe it. This is the world I lived in for 35 years and escaped.

As I showed above that “international law superseding national law” is exactly what Pascal Lamy was yammering about a decade ago and what Klaus Schwab is threatening us with now.

So how do we escape this TRAP if it is being set?

Use USA LAW!

I find it interesting that the internet is FULL of the Nuremberg Code…….

……and the GERMAN/CALIFORNIA LAWYER Reiner Füllmich and 50 Lawyers, but I went nutz trying to find the US LAWS. It took me over ½ hour.

And WHY does Reiner Füllmich have no problem with YouTube???? When everyone else gets the boot?

https://duckduckgo.com/?q=Reiner+F%C3%BCllmich+youtube&t=brave&ia=videos&iax=videos

JW in Germany even brought us this comment:

I watched it for about half an hour and thought it was important enough to post here. The dozens of witnesses/experts that will be speaking in the next days are from around the world…many of the names you may already know.
Day 1 Opening Session of the Grand Jury Proceeding
A group of international lawyers and a judge are conducting criminal investigation modeled after Grand Jury proceedings in order to present to the public all available evidence of Covid 19 Crimes Against Humanity to date against “leaders, organizers, instigators, and accomplices” who aided, abetted, or actively participated in the formulation and execution of a common plan for a pandemic
https://gettr.com/post/psoiulc122

Those are things that make you go HMMMmmm…..

I think Reiner Füllmich and his group is sincere but it is very very possible they are being used.

So after a LOT of digging at Cornell Law I found the provision that covers the situation for the military: 10 U.S.C. § 1107. “This provision prohibits the administration of investigational new drugs, or drugs unapproved for their intended use, to service members without their informed consent.”

And finally after a lot more searching I stumbled across the information that civilians are covered under a FDA Regulation and not a law:
CFR – Code of Federal Regulations Title 21 as of January 6, 2022

Subpart B – Informed Consent of Human Subjects
   § 50.20 – General requirements for informed consent.
   § 50.23 – Exception from general requirements.
   § 50.24 – Exception from informed consent requirements for emergency research.
   § 50.25 – Elements of informed consent.
   § 50.27 – Documentation of informed consent.

[Code of Federal Regulations]
[Title 21, Volume 1]
[CITE: 21CFR50.20]

TITLE 21–FOOD AND DRUGS
CHAPTER I–FOOD AND DRUG ADMINISTRATION
DEPARTMENT OF HEALTH AND HUMAN SERVICES

SUBCHAPTER A – GENERAL
PART 50 — PROTECTION OF HUMAN SUBJECTS
Subpart B – Informed Consent of Human Subjects
Sec. 50.20 General requirements for informed consent.
Except as provided in §§ 50.23 and 50.24, no investigator may involve a human being as a subject in research covered by these regulations unless the investigator has obtained the legally effective informed consent of the subject or the subject’s legally authorized representative. An investigator shall seek such consent only under circumstances that provide the prospective subject or the representative sufficient opportunity to consider whether or not to participate and that minimize the possibility of coercion or undue influence. The information that is given to the subject or the representative shall be in language understandable to the subject or the representative. No informed consent, whether oral or written, may include any exculpatory language through which the subject or the representative is made to waive or appear to waive any of the subject’s legal rights, or releases or appears to release the investigator, the sponsor, the institution, or its agents from liability for negligence.
[46 FR 8951, Jan. 27, 1981, as amended at 64 FR 10942, Mar. 8, 1999]

BUT there is a cockroach in the ointment.

§ 50.24 – Exception from informed consent requirements for emergency research.

[Code of Federal Regulations]
[Title 21, Volume 1]
[CITE: 21CFR50.24]

TITLE 21–FOOD AND DRUGS
CHAPTER I–FOOD AND DRUG ADMINISTRATION
DEPARTMENT OF HEALTH AND HUMAN SERVICES

SUBCHAPTER A – GENERAL
PART 50 — PROTECTION OF HUMAN SUBJECTS
Subpart B – Informed Consent of Human Subjects
Sec. 50.24 Exception from informed consent requirements for emergency research.
(a) The IRB responsible for the review, approval, and continuing review of the clinical investigation described in this section may approve that investigation without requiring that informed consent of all research subjects be obtained if the IRB (with the concurrence of a licensed physician who is a member of or consultant to the IRB and who is not otherwise participating in the clinical investigation) finds and documents each of the following:
(1) The human subjects are in a life-threatening situation, available treatments are unproven or unsatisfactory, and the collection of valid scientific evidence, which may include evidence obtained through randomized placebo-controlled investigations, is necessary to determine the safety and effectiveness of particular interventions.
(2) Obtaining informed consent is not feasible because:
(i) The subjects will not be able to give their informed consent as a result of their medical condition;
(ii) The intervention under investigation must be administered before consent from the subjects’ legally authorized representatives is feasible; and
(iii) There is no reasonable way to identify prospectively the individuals likely to become eligible for participation in the clinical investigation.
(3) Participation in the research holds out the prospect of direct benefit to the subjects because:
(i) Subjects are facing a life-threatening situation that necessitates intervention;
(ii) Appropriate animal and other preclinical studies have been conducted, and the information derived from those studies and related evidence support the potential for the intervention to provide a direct benefit to the individual subjects; and
(iii) Risks associated with the investigation are reasonable in relation to what is known about the medical condition of the potential class of subjects, the risks and benefits of standard therapy, if any, and what is known about the risks and benefits of the proposed intervention or activity.
(4) The clinical investigation could not practicably be carried out without the waiver.
(5) The proposed investigational plan defines the length of the potential therapeutic window based on scientific evidence, and the investigator has committed to attempting to contact a legally authorized representative for each subject within that window of time and, if feasible, to asking the legally authorized representative contacted for consent within that window rather than proceeding without consent. The investigator will summarize efforts made to contact legally authorized representatives and make this information available to the IRB at the time of continuing review.
(6) The IRB has reviewed and approved informed consent procedures and an informed consent document consistent with § 50.25. These procedures and the informed consent document are to be used with subjects or their legally authorized representatives in situations where use of such procedures and documents is feasible. The IRB has reviewed and approved procedures and information to be used when providing an opportunity for a family member to object to a subject’s participation in the clinical investigation consistent with paragraph (a)(7)(v) of this section.
(7) Additional protections of the rights and welfare of the subjects will be provided, including, at least:
(i) Consultation (including, where appropriate, consultation carried out by the IRB) with representatives of the communities in which the clinical investigation will be conducted and from which the subjects will be drawn;
(ii) Public disclosure to the communities in which the clinical investigation will be conducted and from which the subjects will be drawn, prior to initiation of the clinical investigation, of plans for the investigation and its risks and expected benefits;
(iii) Public disclosure of sufficient information following completion of the clinical investigation to apprise the community and researchers of the study, including the demographic characteristics of the research population, and its results;
(iv) Establishment of an independent data monitoring committee to exercise oversight of the clinical investigation; and
(v) If obtaining informed consent is not feasible and a legally authorized representative is not reasonably available, the investigator has committed, if feasible, to attempting to contact within the therapeutic window the subject’s family member who is not a legally authorized representative, and asking whether he or she objects to the subject’s participation in the clinical investigation. The investigator will summarize efforts made to contact family members and make this information available to the IRB at the time of continuing review.
(b) The IRB is responsible for ensuring that procedures are in place to inform, at the earliest feasible opportunity, each subject, or if the subject remains incapacitated, a legally authorized representative of the subject, or if such a representative is not reasonably available, a family member, of the subject’s inclusion in the clinical investigation, the details of the investigation and other information contained in the informed consent document. The IRB shall also ensure that there is a procedure to inform the subject, or if the subject remains incapacitated, a legally authorized representative of the subject, or if such a representative is not reasonably available, a family member, that he or she may discontinue the subject’s participation at any time without penalty or loss of benefits to which the subject is otherwise entitled. If a legally authorized representative or family member is told about the clinical investigation and the subject’s condition improves, the subject is also to be informed as soon as feasible. If a subject is entered into a clinical investigation with waived consent and the subject dies before a legally authorized representative or family member can be contacted, information about the clinical investigation is to be provided to the subject’s legally authorized representative or family member, if feasible.
(c) The IRB determinations required by paragraph (a) of this section and the documentation required by paragraph (e) of this section are to be retained by the IRB for at least 3 years after completion of the clinical investigation, and the records shall be accessible for inspection and copying by FDA in accordance with § 56.115(b) of this chapter.
(d) Protocols involving an exception to the informed consent requirement under this section must be performed under a separate investigational new drug application (IND) or investigational device exemption (IDE) that clearly identifies such protocols as protocols that may include subjects who are unable to consent. The submission of those protocols in a separate IND/IDE is required even if an IND for the same drug product or an IDE for the same device already exists. Applications for investigations under this section may not be submitted as amendments under §§ 312.30 or 812.35 of this chapter.
(e) If an IRB determines that it cannot approve a clinical investigation because the investigation does not meet the criteria in the exception provided under paragraph (a) of this section or because of other relevant ethical concerns, the IRB must document its findings and provide these findings promptly in writing to the clinical investigator and to the sponsor of the clinical investigation. The sponsor of the clinical investigation must promptly disclose this information to FDA and to the sponsor’s clinical investigators who are participating or are asked to participate in this or a substantially equivalent clinical investigation of the sponsor, and to other IRB’s that have been, or are, asked to review this or a substantially equivalent investigation by that sponsor.
[61 FR 51528, Oct. 2, 1996]

And now we go to USA lawyer, Attorney Thomas Renz and his interview on Bannon’s War Room.

Episode 1,619 – Beijing Olympics Fail; Legal/Financial Investigations Of Big Pharma

https://rumble.com/vu5amo-episode-1619-beijing-olympics-fail-legalfinancial-investigations-of-big-pha.html

ROUGH TRANSCRIPT (start at 18:15)

ATTORNEY THOMAS RENZ: We have to get it to the public and that is where the War room is so important.
Se are going to be submitting this to a case in Alabama. We are going to be submitting ths to a number of different places in the military, ahhh I guess law enforcement world. And we are looking to bring this into the civilian law enforcement as well. There is no question as to what is happening. These are major crimes and you know Steve, I don’t know if you have got this but we just yesterday, dated February 4th, got a document from the CDC that re-affirms everything we said last week when we said they know this. If you are interested that document actually says it is was in the meeting yesterday, it was presented yesterday it says the CDC is working to monitor these things and they are monitoring the DOD data. Which indicates to me, I don’t know if you have heard the DOD s response? DOD to me has committed fraud and conspiracy. They have said there baseline data from 2016 to 2020 was wrong. They didn’t notice it until we pointed it out in the whistle blower testimony. But some how even though they didn’t notice it, it magically got corrected in 2021.

I mean seriously, How stupid do they think the American people are?

STEVE BANNON: What about adjudicating this. What about Alabama? (21:40)

RENZ: We have a case in Alabama where we are challenged the EUA authorization of the vaccine….. Balance of harm tests…. Generally you have to show more benefit than injury… we are also challenging on mis branding, because the CDC changed the definition of vaccines so they could call these gene therapies a vaccine. BTW Pfizer and Moderna have admitted they are gene therapy in their documents. And we have challenged it on several other fronts so that’s in court. This document and all this DOD stuff just came to us. We have declarations under penalty of perjury and those declarations will be submitted to the court. They are getting updated right now because we’ve had this new data come forward related to this…. We have been working with attorneys all over the world and around the country… and we have been getting this data out and we are giving it to anyone who wants to use it anywhere they can. And we believe it will help. We have to find the right court like you said. Until we find a court that is willing to listen and have an evidentiary hearing, it’s tough. We are going to have more info on that coming up…..

STEVE: asks about military JAG system and Senator Johnson. Senator Johnson first.

RENZ: The problem for Senator Johnson is he is not getting enough support from other Senators. He has gotten NO RESPONSE from anyone else [including Rand Paul but he does not say that.]

STEVE: What about JAG? [24:50]

RENZ: Since the data has only been out for a week or two, we are working thru a number of JAG officers….. I got another letter this week…. From all places the Texas National Guard, one of the people there saying they are going to reject all the religious exemptions and we don’t want doctors giving medical exemptions. They actually say they view it as a COMMAND ISSUE and not a medical issue. So if a doctor thinks a soldier should not have this for a medical reason, they are to shut-up and take orders according to this document. We submitted that to Senator Johnson as well as some others.

This is a disaster in the military and they have created a situation where it is very very difficult for our solders to fight this. We do however have quite a number of military personnel stepping forward. And quite a number of JAG officers and others who, because of the publicity we have gotten on this, in the last week or so, are now wiling to step up and do something so we’ll see.

It goes on to Edward Dowd about the insurance industry data about unexpected deaths in working age people from there. Steve Bannon mentions that Zero Hedge covered the information given too. Suicide? How Some Life Insurance Companies Are Dealing With Experimental Vaccines Deaths

A very informative earlier video from the War Room showing the DOD changing the data from Thomas Renz. It also has Ed Dowd, a Financial guru who worked for Blackrock…. Yeah, Blackrock. He is calling out not only the vaccine manufacturers but the FDA for massive FINANCIAL fraud similar to ENRON. The video also has an interview with Dr Malone.

From 27:00 to 35:15 minutes

https://rumble.com/vtkou8-episode-1602-the-big-short-pfizer-and-moderna-the-new-enron-are-criminal-ch.html

-GC

Big Pharma – Government – University Collusion on COVID Vaccines

Newly Uncovered COVID Vaccine Contracts Lead Unexpectedly to Academic Corruption and Shill Science Attacks on Honest, Skeptical Scientists

A Gail Combs deep dive into a tangent of Karen Kingston’s latest revelation on Pfizer Comirnaty vaccine deaths and injuries, leads back to the war against truth-telling doctors and scientists – this time by their own CORRUPT university employers.

PREFACE by Wolf Moon

Remember people saying that there was no such thing as the “FDA-approved” Comirnaty version of the Pfizer vaccine in existence?

Well, it turns out that REAL, LIVE COMIRNATY is out there, it has already killed over 50 people [in VAERS – yeah – do the math – x20 (1000), x40 (2000), or x100 (5000)], and – now even more shocking – there was some kind of bureaucratic screw-up in the contract and approval process which makes Pfizer LIABLE for all the deaths and injuries.

Look – I don’t know about the latter part – that’s “the law”, which is basically filled with LIES at this point. Whether any of these people will ever answer for anything is highly debatable, in my opinion.

But that’s not where this goes.

Gail Combs started looking at this video, and discovered ANOTHER scandal – the fact that universities which are silencing and firing honest doctors and scientists are not doing so from some misperception or moral high ground. These universities are turning on honest doctors and scientists because the universities themselves are COMPROMISED – by money, corruption, and the involvement of OTHER scientists at those same universities in the “scamdemic”.

We don’t yet know how deep this goes, but we do know this – the universities are clearly in cover-up mode. It’s not just limited to the vaccines. Fauci’s horrifying executioner remdesivir was forwarded past Trump, thanks to “work” done at one such university.

Follow along with Gail and you’ll see the SHAME of what has happened to many American universities, once bastions of free thinking and HONESTY – now CORRUPT and enemies of TRUTH.

-Wolf

START HERE….

FDA Broke Pfizer’s EUA Shield: Liability Protection Gone, Time To Bring Down The Gavel (10 minutes)

Stew Peters Show, Published January 26, 2022

LINK: https://www.redvoicemedia.com/2022/01/fda-broke-pfizers-eua-shield-liability-protection-gone-time-to-bring-down-the-gavel/

LINK: https://rumble.com/vtcugv-fda-broke-pfizers-eua-shield-liability-protection-gone-time-to-bring-down-t.html

Stew Peters interviews former Pfizer employee and analyst Karen Kingston, who does deep dives into patents and contracts. She found the three major contracts for Moderna, J&J and Pfizer.

Stew: “Karen says she found contracts showing the DOD was in control of what data went to the FDA from vaccine trials. If that is true, then DOD not Big Pharm, was the central figure in any vaccine cover-up…. Military leaders maybe exposed as well…. When the FDA approved the Pfizer vax under the name Cormirnaty, it somehow broke their immunity shield.”

That is not exactly correct. DOD delegated it to Pfizer. With the Pfizer contract with the US Army, it appears that, it was delegated to Pfizer to have the ability to manipulate the data that was submitted to the FDA.

With the Moderna contract for example it shows HHS [US Dept of Health & Human Services] had the authority to manipulate the data that was submitted to the FDA. The contract date is 4/03/2020 for ½ billion $$$ with NIH subsidizing a lot of the contract. It was for producing 100 million mRNA vaccines. The contract (shown) states:

* Contractor shall submit draft FDA submission to BARDA at least 15 days prior to FDA submission
* BARDA will provide feedback to Contractor within 10 days of receipts
* The Contractor MUST address, in writing its consideration of all concerns raised by BARDA prior to FDA Submission.

NOTICE THE DATE 4/03/202. No wonder they wanted to kill HCQ in April!

April 7, 2020 Trump’s Critics Attack His Optimistic Case for Hydroxychloroquine

Karen goes on to say that the contract says that BARDA can provide EDITS to the Data and THAT gets submitted to the FDA. She has never seen anything like this before. This [editing] is why the data was so phenomenally positive. This explains why the Whistle Blowers at Ron Johnson’s Formun found the DOD data had been ‘edited’ to remove the tons of adverse events.

She also said a lot of that contract is redacted including the Key personnel at BARDA .

The J&J contract of an mRNA vaccine was signed 08-Apr-2015 and 60 out of the 90 pages are redacted.

She then goes into the most recent contract. It is a joint mission of Dept of Defense and Dept of Health & Human services who contract with Pfizer/BoiNTech “for the co-development and distribution (excluding China) of a potential mRNA-based Coronavirus vaccine aimed at preventing Covid-19 infection“….. LOTS OF REDACTION….

The Research Collaboration & License Agreement
by and between
PFIZER INC.
and
BIONTECH RNA PHARMACEUTICALS GmbH [Germany]
and
BIOTECH AG
July 20, 2018

Again the DATE July 20 2018 shows mRNA vaccines for the next outbreak of Covid WAS A DONE DEAL!

@5:00 Karen EXPLAINS the OOPS in the Contract. You can not have a contract for commercialization WITHOUT A FDA APPROVAL DATE!!! So how in Hades did they KNOW there would be FDA APPROVAL? This shows it was PRE-PLANNED IN 2018.

@7:00 She also found the Cormirnaty lots used in the USA and the VAERs data

LOT NUMBERS
FD7220
FE3592
FF2587
FF2588
FF2590
FF2593
FF8841
VAERS Dec 2021
Deaths = 51
Disabilities = 94
Hospitalizations 415

So who is BARDA?

Biomedical Advanced Research and Development Authority (BARDA)

WE ARE BARDA
The Biomedical Advanced Research and Development Authority (BARDA), within the Office of the Assistant Secretary for Preparedness and Response in the U.S. Department of Health and Human Services, provides an integrated, systematic approach to the development of the necessary vaccines, drugs, therapies, and diagnostic tools for public health medical emergencies such as chemical, biological, radiological, and nuclear (CBRN) accidents, incidents and attacks, pandemic influenza, and emerging infectious diseases.
Together with our industry partners, BARDA promotes the advanced development of medical countermeasures to protect Americans and respond to 21st century health security threats.

About NIH | National Institutes of Health (NIH)
A part of the U.S. Department of Health and Human Services, NIH is the largest biomedical research agency in the world

So there is your Fauci connection.

And that brings me to the digging I have been doing.

I start with the Chair of the COVID VACCINE ADVISORY BOARD, Hana El Sahly, M.D. of Baylor College of Medicine. She is the one who wrote the Remdesivir paper for Fauci, just in the nick of time so he could get that toxin approved for the use in hospitalized elderly Covid patients.

Baylor College rang a major bell with me. This Yahoo News articles shows why:

August 2, 2021

Dr. Peter McCullough Sued by Baylor After Appearance on Stew Peters Show…

Dr. Peter McCullough is being sued by the healthcare system that just mandated 40,000 employees to get the jab, and they’re doing it out of spite. Here’s the list of emails to those targeting him, if you wish to let them know how you feel….

Sidebar by Wolf – Dr. McCullough on Stew Peters

I dare anybody to watch this and find anything wrong with anything that Peter McCullough is saying. He is basically admitting – at a time when social media was still removing people for saying as much – that the vaccines seemed to no longer be working. And NOW we know why – because of the delta variant.

LINK: https://www.redvoicemedia.com/2021/08/stew-peters-show-dr-peter-mccullough-destroys-vaxx-efficacy-narrative-united-pilots-file-suit-to-stop-mandate/

LINK: https://rumble.com/vlblnr-dr.-peter-mccullough-destroys-vaxx-efficacy-narrative-united-pilots-file-su.html

Dec 20 2021

Doctor fired for spreading COVID misinformation finds supportive Crowd in Bartlesville.

Dr. Peter McCullough, a Dallas cardiologist who is largely discredited by the scientific community [Remember Dr McCullough is the MOST PUBLISHED AUTHOR OF SCIENTIFIC PAPERS IN THE USA.] for his assertions that the COVID-19 vaccines are unsafe and that early treatment options have been suppressed….
While McCullough said that doctors were probably afraid to show up to the event, one of Oklahoma’s top infectious disease physicians, Dr. Anuj Malik, director of infection prevention and control at Ascension St. John, said that the doctors he spoke to were not afraid to attend. They were just not interested in sitting through what would be seen as a “politically-motivated, ideological speech by a modern-day quack.”
Malik said. “With all due respect, none of McCullough’s ideas have been supported by any randomized, double-blind, controlled clinical trials,” [<=== THIS IS ALWAYS THE EXCUSE! NO data is allowed except that PAID FOR BY BIG PHARMA/NIH.]
McCullough shared what he said was a threatening letter from the American Board of Internal Medicine warning that he could lose his certification for spreading misinformation.
There is likely a good reason for his concern about losing certification. A Dallas County court granted a temporary restraining order against him in July on behalf of Baylor Scott & White Health for continuing to claim titles, including vice chief of internal medicine at Baylor University Medical Center, even after he was fired from Baylor in February.
In addition, an article in Medscape, an online global news source for physicians and healthcare professionals, reported that Texas A&M College of Medicine, Texas Christian University and University of North Texas Health Science Center School of Medicine have also cut ties with McCullough for spreading misinformation….

So the Baylor Connection made me curious.

And looky what I found! No wonder Baylor sued Dr McCollough in the hopes of shutting him up as they entice people to be lab rats!

June 8, 2021

Baylor launches clinical trial for COVID-19 vaccine booster

Researchers at the Vaccine and Treatment Evaluation Unit at Baylor College of Medicine have launched a clinical trial to study the safety and efficacy of a booster dose of the Moderna-mRNA-1273 COVID-19 vaccine…. The study is being conducted by the Infectious Disease Clinical Research Consortium in collaboration with the National Institute of Allergy and Infectious Diseases, part of the National Institutes of Health…. “It’s important to determine the magnitude of the immune response after a booster dose in persons who received different vaccines in their initial vaccine regimen. We will also be looking at the safety of a booster dose,” said Dr. Robert Atmar, professor of infectious diseases at Baylor and co-principal investigator of the national study.
This activity is supported by the Infectious Diseases Clinical Research Consortium (IDCRC) through the National Institute of Allergy and Infectious Diseases (NIAID) (UM1AI148684). The IDCRC, consisting of the Vaccine Treatment and Evaluation Units (VTEUs) and the IDCRC Leadership Group, was formed in 2019 to support the planning and implementation of infectious diseases clinical research that efficiently addresses the scientific priorities of NIAID. The consortium includes infectious diseases leaders and clinical researchers from Emory University, University of Maryland School of Medicine, Baylor College of Medicine, Cincinnati Children’s Medical Center and University of Cincinnati, FHI360, Fred Hutchinson Cancer Research Center, Johns Hopkins University, Kaiser Permanente Washington Health Research Institute, New York University, Saint Louis University, Vanderbilt University Medical Center, University of Alabama at Birmingham, University of Rochester, University of Washington, and NIAID. For more information about the IDCRC, please visit www.IDCRC.org.

https://idcrc.org/_includes/images/group_fullv2.jpg

January 21, 2020, Rockville, MD [Above photo]

With presentations from members of the NIAID, the Infectious Diseases Clinical Research Consortium (IDCRC) Leadership Group, and VTEU PIs, the inaugural meeting of the IDCRC began with opening remarks from Anthony Fauci, MD, NIAID director. Session topics featured details on working with the NIAID, the Division of Microbiology and Infectious Diseases, and grants management. Breakout sessions facilitated thoughtful discuss on the consortium’s scientific agenda, flu, STIs, malaria, enteric, and emerging diseases, mentoring and career development, special populations, emerging lab sciences, and operations.
https://idcrc.org/about/index.html

Leadership Operations Center

The IDCRC institutions are leaders of influential infectious diseases, immunology and clinical research programs focused on vaccines and STIs at eight top academic institutions and affiliates across the country. The programs, faculty and collaborators at these institutions have exceptional NIH/NIAID network and international connectivity, a history of performing outstanding ID clinical research and the experience and capability of rapidly responding to ID threats.

Bio Robert Atmar

Dr. Atmar is a member of the Baylor Vaccine Research Center and the federally funded Vaccine Treatment and Evaluation Unit (VTEU). This research group performs Phase I to Phase IV studies of experimental and licensed vaccines, and Dr. Atmar serves as Principal Investigator or Co-Investigator for the clinical trials. Dr. Atmar and the research group have been involved in important studies that led to the licensure of live attenuated and high dose inactivated influenza virus vaccines. They also have performed many studies evaluating vaccines targeting pandemic influenza, including H5N1, H9N2 and H7N9 viruses, and they have evaluated methods to improve vaccine immunogenicity, including delivery of vaccine by different routes of administration, different dosages, and with different adjuvant preparations. The group has also evaluated vaccines targeting other pathogens, including those with importance to biodefense.

NIH Clinical Trials Baylor: LINK

484 ACTIVE Studies found for: Baylor College of Medicine | Recruiting, Enrolling by invitation Studies

2,625 studies found in data base [Baylor College] and 4195 for just Baylor.
24,250 studies – Just college

224,279 studies – University

SEE:
https://clinicaltrials.gov/ct2/results/details?cond=&term=university&cntry=&state=&city=&dist=&Search=Search

>

So is there a Robert Atmar – Hana El Sahly connection???

PubMed(dot)Gov lets you search by author name. So I went looking to see if those two authored papers together.

Search for Atmar R
https://pubmed.ncbi.nlm.nih.gov/?term=Atmar+R&sort=date&size=50

AND WELL WELL WELLL the first two out of the BOX!!!

2022 Jan 26.

SARS-CoV-2 Omicron Variant Neutralization after mRNA-1273 Booster Vaccination.

Pajon R, Doria-Rose NA, Shen X, Schmidt SD, O’Dell S, McDanal C, Feng W, Tong J, Eaton A, Maglinao M, Tang H, Manning KE, Edara VV, Lai L, Ellis M, Moore KM, Floyd K, Foster SL, Posavad CM, Atmar RL, Lyke KE, Zhou T, Wang L, Zhang Y, Gaudinski MR, Black WP, Gordon I, Guech M, Ledgerwood JE, Misasi JN, Widge A, Sullivan NJ, Roberts PC, Beigel JH, Korber B, Baden LR, El Sahly H, Chalkias S, Zhou H, Feng J, Girard B, Das R, Aunins A, Edwards DK, Suthar MS, Mascola JR, Montefiori DC.

N Engl J Med.

And the Affiliations:

• Moderna, Cambridge, MA.
• National Institute of Allergy and Infectious Diseases (NIAID), Bethesda, MD.
• Duke University Medical Center, Durham, NC.
• NIAID, Bethesda, MD.
• Emory University School of Medicine, Atlanta, GA.
• Fred Hutchinson Cancer Research Center, Seattle, WA.
• Baylor College of Medicine, Houston, TX.
• University of Maryland School of Medicine, Baltimore, MD.
• National Institutes of Health, Bethesda, MD.
• Los Alamos National Laboratory, Los Alamos, NM.
• Brigham and Women’s Hospital, Boston, MA.
…..

2022 Jan 26.

Homologous and Heterologous Covid-19 Booster Vaccinations.

Atmar RL, Lyke KE, Deming ME, Jackson LA, Branche AR, El Sahly HM, Rostad CA, Martin JM, Johnston C, Rupp RE, Mulligan MJ, Brady RC, Frenck RW Jr, Bäcker M, Kottkamp AC, Babu TM, Rajakumar K, Edupuganti S, Dobrzynski D, Coler RN, Posavad CM, Archer JI, Crandon S, Nayak SU, Szydlo D, Zemanek JA, Dominguez Islas CP, Brown ER, Suthar MS, McElrath MJ, McDermott AB, O’Connell SE, Montefiori DC, Eaton A, Neuzil KM, Stephens DS, Roberts PC, Beigel JH; DMID 21-0012 Study Group.N Engl J Med.

Affiliation
• From the Departments of Medicine and Molecular Virology and Microbiology, Baylor College of Medicine, Houston (R.L.A., H.M.E.S.), and Sealy Institute for Vaccine Sciences, University of Texas Medical Branch, Galveston (R.E.R.); the Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore (K.E.L., M.E.D., K.M.N.), and the Division of Microbiology and Infectious Diseases (S.C., S.U.N., P.C.R., J.H.B.) and the Vaccine Research Center (A.B.M., S.E.O.), National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda; Kaiser Permanente Washington Health Research Institute (L.A.J.), the Departments of Medicine (C.J., T.M.B., M.J. McElrath) and Laboratory Medicine and Pathology (C.J., C.M.P.), University of Washington, the Vaccine and Infectious Disease Division (C.J., C.M.P., C.P.D.I., E.R.B., M.J. McElrath) and the Statistical Center for HIV/AIDS Research and Prevention (D.S., J.A.Z.), Fred Hutchinson Cancer Research Center, and Seattle Children’s Research Institute (R.N.C.) and the Department of Pediatrics (R.N.C.), University of Washington School of Medicine, Seattle; the Department of Medicine, Division of Infectious Diseases, University of Rochester, Rochester (A.R.B., D.D.), NYU Langone Vaccine Center and Division of Infectious Diseases and Immunology, Department of Medicine, NYU Grossman School of Medicine, New York (M.J. Mulligan, A.C.K.), and NYU Langone Hospital-Long Island Vaccine Center Research Clinic and the Division of Infectious Disease, Department of Medicine, NYU Long Island School of Medicine, Mineola (M.B.) – all in New York; the Departments of Pediatrics (C.A.R.), Microbiology and Immunology (M.S.S.), and Medicine (S.E., D.S.S.), the Center for Childhood Infections and Vaccines (C.A.R.), Hope Clinic of Emory Vaccine Center (S.E.), Emory Vaccine Center, and Yerkes National Primate Research Center (M.S.S.), Emory University School of Medicine, Emory University, and Children’s Healthcare of Atlanta (C.A.R.) – all in Atlanta; the Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh (J.M.M., K.R.); Cincinnati Children’s Hospital Medical Center, Division of Infectious Diseases, University of Cincinnati College of Medicine, Cincinnati (R.C.B., R.W.F.); and FHI 360 (formerly Family Health International) (J.I.A.) and Duke Human Vaccine Institute (D.C.M.) and the Department of Surgery (D.C.M., A.E.), Duke University Medical Center, Durham, NC.

2021 Oct 15

Heterologous SARS-CoV-2 Booster Vaccinations – Preliminary Report.

Authors: Atmar RL,….. El Sahly HM…

EPub 2021 Sept 22
Efficacy of the mRNA-1273 SARS-CoV-2 Vaccine at Completion of Blinded Phase.

El Sahly HM, … COVE Study Group. N Engl J Med. 2021 Nov 4….. Epub 2021 Sep 22….

PubMed lists: COVE Study Group [Corporate Author]

COVE STUDY GROUP:

Hana M. El Sahly, MD is principal investigator for Baylor and under her is listed
Jennifer A. Whitaker, C. Mary Healy, Christine Akamine, Wendy A Keitel, Robert L Atmar, Annette Nagel, Sandra Francisco, Thea Marie Cordero, Janet Brown, Jennifer Christensen, Caroline Doughty-Skierski, Connie Rangel, Carrie Kibler, Coni Cheesman, Lisreina Toro, Chanei Henry, Chianti Wade Bowers, Pedro Piedra, Kathy Bosworth, Kayla Burrell, Jesus Banay, Tykel Eddy, Trent Davis, Shetel Anassi, Yvette Rugeley, Olga Rybina-Willis
…..

So what about the OTHER 15 on the ‘Advisory Board’ I checked, none are in the COVE study group.

….

And one last Baylor – Atmar paper:

SARS-CoV-2 Vaccination During Pregnancy: A Complex Decision.

Wang EW, Parchem JG, Atmar RL, Clark EH.Open Forum Infect Dis.

2021 Apr 10

Abstract
As the first severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines passed UK and US regulatory milestones in late 2020 and early 2021, multiple professional societies offered recommendations to assist pregnant and breastfeeding people as they choose whether to undergo vaccination. Despite such guidance, the lack of data describing vaccine safety, immunogenicity, and efficacy in pregnant and breastfeeding people has made this decision challenging for many. However, even considering the paucity of data, the known risks of coronavirus disease 2019 during pregnancy likely outweigh the not yet fully elucidated risks of SARS-CoV-2 vaccines, which have reassuring safety and efficacy profiles among nonpregnant people.

The Chair of the FDA Vaccines and Related Biological Products Advisory Committee is so compromised she should NEVER have been anywhere near the approval process!

-GC

Summary

After viewing the tape of Dr. Peter McCullough on Stew Peters, I’m both shocked and disappointed that Baylor (IMO both the College of Medicine and the allied University) would do anything except DEFEND Dr. McCullough for simply speaking TRUTH when nobody else dared to say it.

At a time when all of social media was defending what now amounts to SCIENTIFIC ERROR, Baylor – a renowned institution – accused a TRUTH-TELLER of “misinformation” for being on the cutting edge.

To borrow from Trump…… “SAD!”

We know now that everything Dr. Peter McCullough said was not only true, but that the science he cited was LEADING EDGE – pointing in the direction of future findings.

It is not “misinformation” to state scientific and medical findings which are both TRUE and in the process of CHANGING narratives. That IS what science is supposed to do.

China won’t have to fire a SHOT to steal academic leadership from the United States, if Baylor – in TEXAS of all places – is going to hand them scientific superiority on a silver platter.

Get the politics and the self-dealing OUT OF YOUR SCIENCE, BAYLOR.

It is a TRAVESTY for you, Baylor, to let your “big money scientists” force out your TRUTH-TELLERS based on POLITICS and motivated by their own SCIENTIFIC MISJUDGMENTS.

W

**A Book of Some Importance to Baptists**

COVID and BEYOND FAKE NEWS: The “Trusted News Initiative”

A Gail Combs deep dive into a curious item revealed by Robert Malone on Joe Rogan.

https://www.mediainfoline.com/wp-content/uploads/2018/11/Beyond-Fake-News-logo.jpg

Preface by Wolf Moon

Follow along as Gail Combs digs down a snake-infested rabbit hole from something that Dr. Robert Malone mentioned on Joe Rogan.

Once you understand how much preparation went into what is going on RIGHT NOW, you’ll realize that all the usual suspects had a plan, and it’s exactly what we’re seeing now, except they weren’t banking on us understanding their criminal conspiracy.

2:40:50 “We are in an environment where truth and consequences are fungible. This is Modern media management and warfare. The Truth is what those that are managing ‘The Trusted News Initiative’ say it is. “
Dr Robert Malone

From video Dr Robert Malone on Joe Rogan

https://rumble.com/vrv7k1-dr.-robert-malone-on-joe-rogans-podcast.html

CRITICAL TIMELINE

JULY 2019

BBC: Beyond Fake News

Trusted News Initiative
How news organisations can rebuild trust and tackle the next disinformation challenges.
Trust In News
The BBC’s Trusted News Initiative is a partnership that includes organisations such as Facebook, Twitter, Reuters and The Washington Post. It is the only forum in the world of its kind designed to take on disinformation in real time. Now we and our partners are going to share what we’ve all learned about how to tackle disinformation, and you are invited.

Trusted News Initiative or Corrupted News Initiative? Mission: Systematic censorship of the world’s top public health experts

In this August 13, 2021 article for Global Research, Elizabeth Woodworth explains how the Trusted News Initiative (TNI) was formed and what it means to our modern society.
According to Woodsworth, even before the pandemic, there has been a continued increase in public distrust to mainstream media. The TNI began in July 2019 when BBC Director-General Tony Hall convened various media companies and Big Tech companies to “arrive at a practical set of actions we can take together, right now, to tackle the rise of misinformation and bias…[by creating a] global alliance for integrity in news…to promote freedom and democracy worldwide”.
From the beginning, the goal of TNI was to counter “anti-vaxxers [who] were gaining traction on social media as a part of a “fake news” movement spreading “misleading and dangerous information”….
TNI has become an instrumental tool for the suppression of life-saving information….

Trump-Ukraine impeachment scandal: timeline of key events

YEAR 2019

18 July Trump issues instructions to withhold $392m in military aid from Ukraine

25 July Trump and Zelenskiy speak on the phone.

12 August A whistleblower complaint is filed.

24 September The House speaker, Nancy Pelosi, announces a formal impeachment inquiry into Trump’s actions.

6 October Lawyers for the first whistleblower say they are now representing a second.

8 October The state department prevents Gordon Sondland, US ambassador to the EU and a Trump donor, from testifying to a congressional impeachment hearing.

October 18 Event 201

https://i.ytimg.com/vi/YxxNZ5u6JXo/maxresdefault.jpg

Event 201

The Johns Hopkins Center for Health Security in partnership with the World Economic Forum and the Bill and Melinda Gates Foundation hosted Event 201, a high-level pandemic exercise on October 18, 2019, in New York, NY. The exercise illustrated areas where public/private partnerships will be necessary during the response to a severe pandemic in order to diminish large-scale economic and societal consequences.

….

October 18 – 28, 2019

https://obj.shine.cn/files/2019/10/18/b9afeeca-61e9-4c63-b79d-44a28dd12340_0.jpg

CISM Military World Games – U.S. Department of Defense

Top U.S. military athletes are competing against their counterparts from more than 100 nations during the 2019 Military World Games in Wuhan, China, Oct. 18-28.

Did the Military World Games Spread COVID-19?

The 2019 Military World Games, branded the “Peace Games,” was the largest military sports event ever held in China. More than 9,000 athletes representing the militaries of more than 100 countries competed in 27 sports…

Whistleblower: 2019 Wuhan Military Games Were China’s First Intentional COVID Super-Spreader Event

On July 21, 2021, Lawrence Sellin, Ph.D. broke the news on The Gateway Pundit from a China source that the release of COVID-19 at the 2019 Military World Games in Wuhan was a test of the longer-term effects of that type of bioweapon because foreign visitors to the Games would carry it back to their own countries and the consequences could be observed. . .

Letter to Congress:

https://gallagher.house.gov/sites/gallagher.house.gov/files/Letter_World%20Military%20Games_6.21.pdf

December 11, 2019 The Hill

Scientist claims first known COVID-19 case was Wuhan market vendor

Michael Worobey, head of the Department of Ecology and Evolutionary Biology at the University of Arizona, wrote in a piece published in the journal Science that a female seafood vendor who worked at the live animal market in Wuhan and became ill on Dec. 11, 2019, was likely the first known case of COVID-19.

December 18 – House voted to impeach Trump

CDC Museum COVID-19 Timeline

December 31, 2019 The World Health Organization China Country Office is informed of a number cases of pneumonia of unknown etiology…

January 2, 2020 The World Health Organization activates its incident management system…

January 5, 2020 CDC’s National Center for Immunization and Respiratory Diseases (NCIRD) activates a Center Level Response…

January 7, 2020 Chinese authorities identify and isolate a novel coronavirus….

January 7, 2020
CDC establishes a 2019-nCoV Incident Management Structure to guide the response….

[January 16, 2020 – Articles delivered & Impeachment Trial began in the Senate]
January 17, 2020 CDC begins screening passengers on direct and connecting flights from Wuhan, China

January 17, 2020 CDC deploys a team to Washington state to assist with contact tracing efforts in response to the first reported case

January 20, 2020 CDC confirms the first U.S. laboratory-confirmed case of COVID-19 in the U.S.

January 21, 2020 CDC transitions from a Center-led Incident Management Structure to an Agency-wide Structure and activates its Emergency Response System

[January 25, 2021, House impeachment managers delivered the article of impeachment to the U.S. Senate.]

February 5, 2020 Senate voted to acquit

March 27 2020 CARES act passed It pays hospitals to kill elderly covid patients. See Sec. 3710….. Assoc of American Physicians & Surgeons : Biden’s Bounty on your Life

The Timeline seems to indicate that President Trump was kept distracted while the Democrats and Mr Global put the pieces in place to unleash the Plandemic and force the world to take the clot shot.

…………….

The NUREMBERG CODE is worth rereading before we go down into the snake pit.

https://pbs.twimg.com/media/FIQ9KIsVIAAeZ17.jpg

While Collins, Fauci, hospitals and medical boards moved to silence and censor ALL opinions by dissenting experts, the Trusted News Initiative also muzzled anyone else not advocating for the Clot Shot. However Mr Global went even further than censorship and threatening jobs and medical licenses.

TEN NIH STUDIES ON ‘VACCINE REFUSAL’

‘Vaccine Refusal’ is considered a ‘condition or disease’ that needs ‘treatment’ The following are trials to determine how to ~~convince~~ brainwash people into consenting to taking an experimental drug WITHOUT giving them full disclosure.

NEW TRIAL!!! COVID-19 Messaging for Vaccination

MIT Cambridge, MA ; Behavioral: Doctor Videos

Behavioral: Sharing Videos
Behavioral: Sharing Videos (Influencers)
(and 3 more…)

Collaborators:

Facebook, Inc. aka Mark Zuckerberg who was Caught Stealing Election With Ballot Drop Boxes

And his CHINESE WIFE (Red Diaper Baby from China?)

She was mostly raised by her Chinese grandmother, who spoke no English. She was a very dignified woman who clearly was a huge influence in Priscilla’s life…. But the precise details of how the family arrived in America are unclear. Reports in China say they came originally from the city of Xuzhou in eastern Chandong province, also the home city of Rupert Murdoch’s wife Wendi Deng. Others say that the family lived in Nanjing, an industrial town 150 miles west of Shanghai, before leaving to live first in Hong Kong and later in the US.
A source at the Asian-American Civic Association in Boston said it was ‘highly likely’ the family spent time in a refugee camp, either in Hong Kong or on arrival in the US.
Priscilla’s father said he was a refugee who had lived in Vietnam, according to Thai-born Napat
Records show Dennis,[Her father] who now owns a small wholesale fish business, was given a social security number as an ‘Asian Refugee’ between April 1975 and November 1979.

Code3

Stanford University

Harvard University

Yale University

Johns Hopkins University

Massachusetts General Hospital

Ludwig-Maximilians – University of Munich

National Institutes of Health (NIH)

Study Description

Brief Summary:

This study will distribute videos of health professionals encouraging Covid-19 vaccination to a large sample of Facebook users, and will test the most effective ways to maximize diffusion of this vaccine-related content to increase vaccination rates. The study sample will be U.S. states where vaccination rates remained low in fall 2021. The experimental design is an RCT with 4 groups, randomized at the county level: 1) a control group which receives no intervention, 2) a treatment group in which Facebook users receive ads which include videos of health professionals telling them to get vaccinated, 3) a treatment group in which Facebook users receive ads which include videos of health professionals encouraging them to help their friends to get vaccinated, and 4) a treatment group in which Facebook users receive ads which include videos of health professionals encouraging them to get their most influential friends to help their friends get vaccinated. In treatments 3 and 4, participants will have the option to sign up to be a “vaccine ambassador,” in which case they will get notifications when the study team posts new vaccine-related content, and will receive reminders about encouraging their friends to be vaccinated. The vaccine ambassadors will also be entered into a lottery to win prizes. The study team is building a website to host the videos of health professionals which answer common questions about Covid-19 vaccination. The investigators will measure engagement with the vaccine-related content as well as assess effects on vaccination rates at the county level.

Interventional (Clinical Trial)
Estimated Enrollment :	40,000,000 participants
Allocation:	Randomized
Intervention Model:	Parallel Assignment
Intervention Model Description:	There are four arms in the study which geographic areas are assigned to in parallel. The geographic areas in the three treatment arms will receive a Facebook ad campaign over the same time period to one another.
Masking:	None (Open Label)
Primary Purpose:	Treatment
Official Title:	Increasing the Effectiveness and Diffusion of COVID-19 Messaging for Vaccination
Actual Study Start Date :	December 22, 2021
Estimated Primary Completion Date :	January 2022
Estimated Study Completion Date :	June 2022

THAT IS 40 MILLION PEOPLE!!!

……….

A Tailored, Health Communication Intervention for HPV Vaccine Hesitant Families – Meharry Medical College, Nashville TN

……….

COVID-19 Vaccine Hesitancy and Dental Faculty Staff Members

– Ain Shams University Cairo, Egypt

………..

Development and Testing of ADEPT: A Parent Decision Support for Childhood Vaccinations

— Duke University Health System, Durham, NC ( Childhood vaccination decision support tool) Principal Investigator Lavanya Vasudevan, Ph.D.

Collaborator: National Institutes of Health (NIH) 1KL2TR002554 ( U.S. NIH Grant/Contract )

………..

Clinic-based HPV and COVID-19 Vaccine Promoting Intervention for AfAm Adolescents in Alabama

– University of Alabama at Birmingham (Behavioral: Intervention)

Contact: Henna Budhwani, PhD, MPH

……….

– Annenberg School Philadelphia, PA

Behavioral: Online Social Network and Collective Intelligence Intervention :

Behavioral: Independent Control

Collaborators: University of California, Davis, University of California, San Francisco, University of California, Berkeley

Brief Summary:

Social technologies for health have already become essential means for providing underserved populations greater social connectedness and increased access to novel health information. However, these technologies have also had negative unintended consequences. The resulting digital divide in social technology takes many forms – from explicit racism that excludes African American and Latinx populations from the resources enjoyed by White and Asian members of online communities, to self-segregation for the purposes of identity preservation and community-building that unintentionally results in limited informational diversity in underserved communities. The result is an often unnoticed, but highly consequential compounding of inequities.
This research seeks to use an online social network approach to address these challenges, in which the investigators demonstrate how reducing the online levels of network centralization and network homophily among African American community members directly increases their productive engagement with health-promoting information.

………..

Project 2VIDA! COVID-19 Vaccine Intervention Delivery for Adults in Southern California –

San Ysidro Health Chula Vista CA;
Care View Health Center San Diego, CA;
San Ysidro Health Care View Health Center, San Diego, CA; and 3 more…
Principal Investigator: Argentina Servin, MD, MPH, Asst Prof,
Sponsors/Collaborators National Institute on Minority Health and Health Disparities (NIMHD)
Behavioral: COVID-19 Individual Awareness and Education;
Behavioral: COVID-19 Community Outreach & Health Promotion;
Behavioral: COVID-19 Individual Health Education & Linkages to Medical and Supportive Services;
Biological: Pop-up community vaccination sites

-GC

Conclusion by Wolf Moon

Do you see it now? They knew exactly what they were doing. Schiff’s kabuki with Zuckerberg was like a GO signal to start the censorship.

That creepy pedophile loser, the compromised Dem Rep on the committee that’s SUPPOSED to control the IC, but is in fact CONTROLLED BY IT, signals to the IC social media that’s SUPPOSED to serve us, but in fact SERVES THE IC, that they need to start censoring us by removing InfoWars and Natural News.

It ALL makes sense now.

CHICOMS. These people are no better than CHICOMS. Allies of the enemies of America. Traitors of the worst kind.

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
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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
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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)
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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.
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LECTURESHIPS, SEMINAR INVITATIONS, AND VISITING PROFESSORSHIPS:
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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
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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

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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)

ANTI-HOARDING LAWS, THE GREAT RESET AND TRUMP

Introduction

As a side note, we have laws, regulations, Executive Orders, all open to the public PLUS classified Presidential Policy Directives. This means we would not know exactly what President Trump actually did in preparation for the Election Steal.

I do not want to scare everyone so I am going to start by discussing The Devolution Series by Patel Patriot first. Please at least skim this series.

I like to connect dots and I see a few that Patel Patriot missed so I am going to point them out.

In Part 2 – The Defense Intelligence Agency and the Defector He mentions

Vice Minister Dong Jingwei of the Ministry of State Security (MSS) defected from China to the United States on Feb 10th, of 2021. Dong was previously the chief of counterintelligence for the MSS….
Patel Patriot

The rest of the information is about how Biden’s admin was COMPLETELY UNAWARE OF THIS DEFECTOR…. HMMmmmm

Patel Patriot goes on to say:

DIA leadership (Trump appointed Lt. Gen Berrier) believes there are “Chinese spies or sources inside the FBI, CIA, and several other federal agencies.” He has proof. The defector brought “terabytes” of data with him. Included in that data is the “names of Chinese Spies working in the US” and “Names of US Citizens who provide intel to China” as well as Hunter “(and Joe’s) business dealings with Chinese entities.”
….The implications here are MASSIVE.
The DIA (the principal source of intelligence for COMBAT RELATED MISSIONS) kept the defector a secret because the President [Biden] was implicated by the information the defector provided.
Patel Patriot

HOWEVER the last time Dong was seen in public was September 2020 just before the US elections…

Another clue that Patel Patriot missed, is WHY would Dong escape only to run to a country RUN BY A CHINESE PUPPET? You would have to have a death wish to do that. However if you had the Chinese playbook on HOW China was going to steal the 2020 election and install their puppet, you just might risk running BEFORE the 2020 elections.

In Devolution – Part 12 – “Playbook” Patel Patriot drops a second bit of interesting information. If you read nothing else, READ PART 12. It explains the ‘BLACKMAIL’ used to oust President Trump and keep him from fighting back. (See also Devolution – Part 6 —Antifa & the Capitol Riot for the other bit of blackmail.)

..As we go further, you’ll see exactly what is meant by “state destabilization,” but the biggest take away here is knowing all Color Revolutions closely follow the same template. We will be closely examining that template shortly…
Patel Patriot

…before we get too far, we need to reflect on something from that last screenshot.

…the very same regime change professionals who run Color Revolutions on behalf of the US Government in order to undermine or overthrow alleged ‘authoritarian’ governments overseas, are running the very same playbook to overturn Trump’s 2016 victory and to pre-empt a repeat in 2020.
Patel Patriot

PURPLE REVOLUTION anyone?

….Just the TIP
One of the more interesting and sinister developments that took place in 2020 was creation of the Transition Integrity Project (TIP). On August 3rd of 2020, the Transition Integrity Project released a report titled “Preventing a Disrupted Presidential Election and Transition.”
Patel Patriot

This group WAR GAMED various outcomes of the 2020 election and what their response would be.

What they do not mention, but is implied in the statement “…to Spur all Stakeholders to Action…” means continuous violent rioting by BLM & ANTIFA if Trump took and held office in 2021 — THINK Ukraine.

Remember that the lead up to the 2020 election was BLM & ANTIFA riots? (Where are they now?)

Remember DEFUND THE POLICE! implemented in many US cities?

Remember DemonRat Prosecutors and their revolving door for violent protesters?

What these bastards were going to do is escalate those riots into full scale Civil War in every democrat run city to bait President Trump into putting the riots down and then getting the Fake News to claim he was another ‘Hitler’ giving Congress a pretext to impeach him if the first four methods did not work. Aka “Overthrow alleged ‘authoritarian’ regime of Donald Trump.

However the most interesting sentence is this:

Participants got to choose whether their involvement would be publicly disclosed or not so we don’t have a full list…
Patel Patriot

Add that to the information from Vice Minister Dong Jingwei and it seems certain that President Trump DID have the connections between the Transition Integrity Project and China. We also know that Mike Pompeo warned certain state governors about their cozy ties with China.

Devolution is based on the WAR TIME authority of a President. Thanks to the precedence set by President Lincoln, a declaration of war by Congress is NOT NECESSARY if the USA is attacked. Patel Patriot goes into this in depth HERE.

The court ruling in the case of Lincoln:

While President Trump would not make an open declaration of War against China, he could and would take the necessary steps to defend the USA. On top of that Congress Declared War on Sept. 14, 2001 and it has been ongoing ever since.

That brings us to a very important bit of information:

The key phrase that Patel Patriot does not point out is:

Devolution is the capability to transfer statutory authority and responsibility from the organizations primary operating staff and facilities to OTHER DESIGNATED STAFF AND ALTERNATE LOCATIONS…
Patel Patriot

You want to get rid of the Deep State and the Corruptocrats? You set up a parallel government with OTHER PERSONNEL.

HOARDING

Most of us are familiar with ‘The Great Reset,’ Klaus Schwab and the World Economic Forum. This article goes into the details.
The Global Elite’s Plan to Radically Remake Our Economic and Social Lives

To put their plan in place they have to ‘BREAK’ the American people by destroying our freedoms, our will and our economy. If you look at what Biden is doing from the point of view of crashing the US economy it makes sense. Bring in millions of third worlders looking for a handout. INSISTING workers and school kids take the Clot Shot, destroy our import/export of goods and lastly, disrupting our food supply chain.

Sundance has been warning that food shortages are coming so we have been discussing preparation. There is one major fly in the ointment – Anti-Hoarding E.O.s and laws.

How will they know where you live?

Census GPS-tagging your home’s front door Coordinates being taken for every residence in nation

“According to an online Yahoo program, the Global Position System coordinates for the White House, probably one of the best-known publicly owned buildings in the world, are 38.898590 Latitude and -77.035971 Longitude. And since you know that, it’s no big deal for the White House to know the coordinates for your front door, is it?

Some people think it is, and are upset over an army of some 140,000 workers hired in part with a $700 million taxpayer-funded contract to collect GPS readings for every front door in the nation.
The data collection, presented as preparation for the 2010 Census, is pinpointing with computer accuracy the locations and has raised considerable concern from privacy advocates who have questioned why the information is needed. The privacy advocates also are more than a little worried over what could be done with that information.

Enhancing the concerns is the Obama administration’s recent decision to put White House Chief of Staff Rahm Emanuel in an oversight role over the census, which will be used to determine a reapportionment of congressional seats and could be used to solidify a single political party’s control over the nation, its budget, military and future…
Real Texas Cowgirl

HOW would they know who is hoarding?

Well there are your credit card records and those handy ‘Rewards Cards’ that let you buy featured produces at a discounted price. Many grocery stores have them.

That they are doing this type of snooping is established.

Hospitals to begin monitoring your credit card purchases to flag ‘unhealthy’ habits

What you buy at the grocery store, where you live, and even your membership status at the local gym are all subject to a new data collection scheme by the American medical system. Reports indicate that hospitals and doctors’ offices all across the country are now collecting this and other personal information in order to target individuals deemed to have “unhealthy” lifestyle habits that put them at high risk of disease.
Bloomberg reports that hospital systems in both North and South Carolina as well as Pennsylvania have already begun tracking people’s food-purchasing habits by spying on them through public records and credit card transactions. Carolinas HealthCare System (CHS), which operates some 900 care centers throughout the Carolinas, has teamed up with a data-mining company to compile and track this information for the later purpose of calling “high-risk” folks and urging them to make a change.
“What we are looking to find are people before they end up in trouble,” stated Michael Dulin, chief clinical officer for analytics and outcomes at CHS, to Bloomberg. “The idea is to use big data and predictive models to think about population health and drill down to the individual levels to find someone running into trouble that we can reach out to and try to help out.”.
Jonathan Benson of Natural News August 10, 2014

I copied this comment back around 2008 during the ‘Farm Wars’ It may have been from a Yahoo group or from NoNais, I am not sure but it is a very telling comment.

I have been involved in a discussion about a USDA employee who visited an individual’s home in the Pacific NW and began asking a lot of questions about the person’s food storage practices & their raising of small livestock (chickens).…
I agree completely with the “do it quietly” mind set…. But in this case the Dept. of Ag was visiting all the homes in a neigborhood.
“A person from the US Dept of Agriculture came to my door and asked me a bunch of questions which boiled down to whether or not I store food. My daughter has ONE pet chicken, and this woman was looking at the chicken and asking if I have any others, etc. Do I garden? Any other animals? Also, she had a list in her hand of all my neighbors, and was planning to see all of them, too.”
Actually, I did see a congresscritter once who stated that the government really needed to either stop or put some guidelines out about people raising their own food. He said that most people did not know how to do it safely.
Gardening is the same way. Technically it is illegal….I couldn’t find the garden thing specifically. This was something a professor pointed out to me, though I did find it odd as well. It was somehow tied into “affecting interstate commerce” This clause however, seems to provide a loophole for anything the govt wishes to do.
Unknown

“…Gardening is the same way. Technically it is illegal….” And she is correct.

Trojan Horse Law: The Food Safety Modernization Act of 2009

…. Lori Robertson of FactCheck.org, who is not a lawyer (she has a B.A. in advertising), claims the bill doesn’t apply to “that tomato plant in your backyard.”
As a lawyer, I am skeptical of this claim (I co-represented the prevailing defendant in the last successful constitutional challenge to federal regulation under the interstate commerce clause, United States v. Morrison (2000), one of only two cases in 70 years in which a challenge was successful). Congress’s power under the Constitution’s Commerce Clause is almost unlimited in the eyes of the courts, and thus can reach the “tomato plant in your backyard.”
…..Ignorance about the law’s broad reach (and how it will be construed by the courts) has thwarted opposition to the bill, which will likely pass Congress. For example, a newspaper claims the bill “doesn’t regulate home gardens.” The newspaper probably assumed that was true because the bill, like most federal laws, only purports to reach activities that affect “interstate commerce.” To an uninformed layperson or journalist, that “sounds as if it might not reach local and mom-and-pop operators at all.” (The bill’s sponsor, Rep. Rosa DeLauro, has sought to forestall opposition to her bill by falsely claiming that that “the Constitution’s commerce clause prevents the federal government from regulating commerce that doesn’t cross state lines.”)

But lawyers familiar with our capricious legal system know better. The Supreme Court ruled in Wickard v. Filburn (1942) that even home gardens (in that case, a farmer’s growing wheat for his own consumption) are subject to federal laws that regulate interstate commerce. Economists and scholars have criticized this decision, but it continues to be cited and followed in Supreme Court rulings, such as those applying federal anti-drug laws to consumption of even home-grown medical marijuana. Indeed, many court decisions allow Congress to define as “interstate commerce” even non-commercial conduct that doesn’t cross state lines — something directly at odds with Rep. DeLauro’s claims.
Hans Bader

And just to give you the warm fuzzies…

Why Is the USDA Buying Submachine Guns with 30-Round Magazines? Are those bullets for our livestock or for us farmers?

And that brings us to……

THE GOVERNMENT AND ANTI-HOARDING

I am using a 2005 article as my jumping off point:

Can Our Government Really Tell Us How Much Food and Supplies We Can Keep?

The short answer is YES, in a roundabout way. Due to numerous discussions questioning the existence of federal anti-hoarding legislation, I wanted to see if such Executive Orders had been written….
Holly Deyo: hollyd@standeyo.com

And then she provides a list of E.O.s now superseded by Obama’s Executive Order 13603

Sec. 201. Priorities and Allocations Authorities. (a) The authority of the President conferred by section 101 of the Act, 50 U.S.C. App. 2071, to require acceptance and priority performance of contracts or orders (other than contracts of employment) to promote the national defense over performance of any other contracts or orders, and to allocate materials, services, and facilities as deemed necessary or appropriate to promote the national defense, is delegated to the following agency heads:

(1) the Secretary of Agriculture with respect to food resources, food resource facilities, livestock resources, veterinary resources, plant health resources, and the domestic distribution of farm equipment and commercial fertilizer;

(2) the Secretary of Energy with respect to all forms of energy;
(3) the Secretary of Health and Human Services with respect to health resources;

(4) the Secretary of Transportation with respect to all forms of civil transportation; (5) the Secretary of Defense with respect to water resources; and

(6) the Secretary of Commerce with respect to all other materials, services, and facilities, including construction materials.
E.O. 13603

However she did not actually look at the 1950 DEFENSE PRODUCTION.

SUBCHAPTER I—PRIORITIES AND ALLOCATIONS Section 4512.

§4512. Hoarding of designated scarce materials

In order to prevent hoarding, no person shall accumulate
(1) in excess of the reasonable demands of business, personal, or home consumption, or
(2) for the purpose of resale at prices in excess of prevailing market prices,
materials which have been designated by the President as scarce materials or materials the supply of which would be threatened by such accumulation. The President shall order published in the Federal Register, and in such other manner as he may deem appropriate, every designation of materials the accumulation of which is unlawful and any withdrawal of such designation. In making such designations the President may prescribe such conditions with respect to the accumulation of materials in excess of the reasonable demands of business, personal, or home consumption as he deems necessary to carry out the objectives of this chapter. This section shall not be construed to limit the authority contained in .
(Sept. 8, 1950, ch. 932, title I, §102, ; July 31, 1951, ch. 275, title I, §101(b), .)

FEMA’s job is the orderly distribution of supplies. The above 1950 law confiscates and the 1988 law (below) distributes.

FEMA:

Robert T. Stafford Disaster Relief and Emergency Assistance Act, PL 100-707, signed into law November 23, 1988; amended the Disaster Relief Act of 1974, PL 93-288. This Act constitutes the statutory authority for most Federal disaster response activities especially as they pertain to FEMA and FEMA programs.
FEMA

Stafford Act, as Amended

Sec. 413. Food Commodities (42 U.S.C. 5180)
(a) Emergency Mass Feeding – The President is authorized and directed to assure that adequate stocks of food will be ready and conveniently available for emergency mass feeding or distribution in any area of the United States which suffers a major disaster or emergency.
(b) Funds for Purchase of Food Commodities – The Secretary of Agriculture shall utilize funds appropriated under section 612c of title 7, to purchase food commodities necessary to provide adequate supplies for use in any area of the United States in the event of a major disaster or emergency in such area.
Stafford Act from FEMA website

However she is correct about state laws and gives a list of titles to look under.

THE GRAIN CRISIS

Of course you need an EXCUSE before you can start confiscation of Food, Cars Tractors, Equipment and Farmland So Mr Global set up the situation over the decades since WWII.

In 2008, the financial traders (and banks) saw food as the next big moneymaker. They also set up the USA for starvation down the road.

How Goldman gambled on starvation
Speculators set up a casino where the chips were the stomachs of millions. What does it say about our system that we can so casually inflict so much pain?
Johann Hari

Food shortfalls predicted: 2008

The agricultural sector was one of the areas we found most attractive in 2007. We expect that will remain the case. Long term global price and demand trends remain positive…
In summary, we have record low grain inventories globally as we move into a new crop year. We have demand growing strongly. Which means that going forward even small crop failures are going to drive grain prices to record levels. As an investor, we continue to find these long term trends…very attractive.
Joseph Dancy

And by the same outfit

Investing in Farmland: 4 Ways to Play the Agricultural Boom

By the NGO Grain (dot) Org: Financial Speculators Reap Profits From Global Hunger

By a blogger: Biofuel starvation wasn’t “unforeseen consequences”

And Counter Currents: Financial Speculators Reap Profits From Global Hunger April 28, 2008

A series of reports in the international media have drawn attention to the role of professional speculators and hedge funds in driving up the price of basic commodities—in particular, foodstuffs. The sharp increase in food prices in recent months has led to protests and riots in a number of countries across the globe.
Stefan Steinberg

However the KEY for the USA IN 2022 was the destruction of US grain reserves and grain elevators.

Want food security? Bring back a national grain reserve

September 21, 2012|– To blunt the ravages of drought and market greed, we need a national grain reserve….our country cannot even threaten to bolster the national supply because the United States does not possess a national grain reserve. Such was not always the case….
Frederick Kaufman

July 22, 2008 letter to President Bush from the Grain Traders

Recently there have been increased calls for the development of a U.S. or international grain reserve to provide priority access to food supplies for Humanitarian needs. The National Grain and Feed Association (NGFA) and the North American Export Grain Association (NAEGA) strongly advise against this concept..Stock reserves have a documented depressing effect on prices… and resulted in less aggressive market bidding for the grains.…
Kendell Keith, President National Grain and Feed Association
Gary C. Martin, President and CEO North American Export Grain Association

So over a decade ago US food reserves were ABOLISHED but that was not enough. MORE ACTION WAS NEEDED. Ice Age Farmer in this 13 minute video goes over the last moves designed to lead to major food shortages.

China HOARDS ONE HALF THE WORLD’S GRAINS….

Australia BANS unvaxed farmers from selling grain….

Unvaxed Truckers WILL NOT DRIVE… (Check out the comments too)

https://www.youtube.com/watch?v=g8V6CxBIdo8

Moar AND Logic — Vaccines

a guest post by Gail Combs

(with a FREE SPEECH preface by Wolf Moon)

PREFACE

I want to tell you all something RIGHT UP FRONT.

I have not read this post AT ALL. And I’m not going to read it. I’m going to publish it, and THEN READ IT.

WHY AM I DOING THIS, YOU MIGHT ASK.

It is very simple. I support free speech, and I am especially concerned about CENSORSHIP of viewpoints on vaccination. I am personally pro-vaccination, but I think that the anti-vaxxers have found a WEALTH of valid concerns that need to be addressed by a combination of objective and imaginative investigation, honest admission, political enlightenment, and consumer CHOICE.

The COMMUNISTS in America are NOT doing it right. The real question is WHY NOT?

Vaccines are a PRODUCT – not a CHEMICAL TATTOO that the state has a right to force upon our bodies. GET REAL. Vaccines need the FREE MARKET to prove their worth – not socialist coddling of substandard products to be forced upon us like poisonous Chinese dog treats.

If you are old enough to remember the vaccine SANITY that we had in America before the sabotage presidency of crypto-socialist BILL CLINTON and his horrible co-President wife Hillary Clinton, of WACO fame, then you realize that all of this CRAP about vaccines is utterly unnecessary.

Let us just GO BACK TO WHAT WORKED BEFORE COMMUNISM.

M-KAY?

NOW – I believe that Adam Schiff is starting a “war on anti-vaxxers” in preparation to “war on Trump’s base”. I will be posting more about this soon. But before that, I’m going to let some FREE SPEECH about vaccination happen HERE AND NOW.

Enjoy!

-WOLF MOON

Moar AND Logic — Vaccines

by Gail Combs

GENERAL COMMENT

Perhaps the hardest concept for Americans to learn is Our Ruling Class views us with contempt. They do not hate us. To hate you have to view a person as an equal. The Ruling Class does not consider us equals, some do not even consider us ‘human’!!! We are just ‘Human Resources’ for them to use as they please. Once you realize they view us as free range slaves or cattle (chattel) their inhumane treatment of us becomes comprehensible and this plays into their views on vaccination. As long as THEY make money and the ‘Human Resource’ losses are ‘acceptable’ they don’t care if we are injured or die.

This is the best overall explanation I have seen of what we face in America today:

July 16, 2010 America’s Ruling Class — And the Perils of Revolution by Angelo M. Codevilla

“…No prominent Republican challenged the ruling class’s continued claim of superior insight, nor its denigration of the American people as irritable children who must learn their place. The Republican Party did not disparage the ruling class, because most of its officials are or would like to be part of it.

Never has there been so little diversity within America’s upper crust. Always, in America as elsewhere, some people have been wealthier and more powerful than others. But until our own time America’s upper crust was a mixture of people who had gained prominence in a variety of ways, who drew their money and status from different sources and were not predictably of one mind on any given matter….

Today’s ruling class, from Boston to San Diego, was formed by an educational system that exposed them to the same ideas and gave them remarkably uniform guidance, as well as tastes and habits. These amount to a social canon of judgments about good and evil, complete with secular sacred history, sins (against minorities and the environment), and saints. Using the right words and avoiding the wrong ones when referring to such matters — speaking the “in” language — serves as a badge of identity….

The two classes have less in common culturally, dislike each other more, and embody ways of life more different from one another than did the 19th century’s Northerners and Southerners — nearly all of whom, as Lincoln reminded them, “prayed to the same God.” By contrast, while most Americans pray to the God “who created and doth sustain us,” our ruling class prays to itself as “saviors of the planet” and improvers of humanity. Our classes’ clash is over “whose country” America is, over what way of life will prevail, over who is to defer to whom about what….”

We have already noted the consolidation of the trans-national corporations.

Daniel Estulin in his Bilderberg Speech at EU Parliament says:

“Bilderberg organization is dynamic…. Members come and go, but the system itself has not changed. It is a self-perpetuating system, a virtual spider web of interlocked financial, political, economic and industry interests. Not One World Government or New World Order as too many people mistakenly believe. Rather, the ideology is of a ONE WORLD COMPANY LIMITED….
The idea behind each and every Bilderberg meeting is to create what they themselves call THE ARISTOCRACY OF PURPOSE between European and North American elites on the best way to manage the planet. In other words, the creation of a global network of giant cartels, more powerful than any nation on Earth, destined to control the necessities of life of the rest of humanity, obviously from their vantage point, for our own good and in our benefit – THE GREAT UNWASHED AS THEY CALL US.

In this 2/29/2016 video OT Ben Stein call Trump people the “unwashed”

Later in the year, on 08/26/2016
PeterStrzok texted “Just went to a southern Virginia Walmart. I could SMELL the Trump support…”
Page replys “Yep….”

Obama’s Science Czar, John Holdren certainly agrees and takes it a step further. He thinks it takes ” essential early socializing experiences”aka brainwashing to “ultimately develop into a human being.” GEE, does that mean IF you do not have the CORRECT ‘ socializing experiences’ you are not human?

Holdren, wrote on page 235 in “Human Ecology,” (1973) co-authored with Paul and Anne Ehrlich.

The fetus, given the opportunity to develop properly before birth, and given the essential early socializing experiences and sufficient nourishing food during the crucial early years after birth, will ultimately develop into a human being,”

More bizarre quotes: link

Michaelh made a comment on June 12, 2019 at 02:22
The interesting part of the comment is this:

….He told the other doctor he could solve his problem, but the other doc was skeptical. Later he saw the woman in question and she went on at length about the dangers of vaccines and all the information she had gathered online, listening to her intently and patiently the whole time. At the end of it he asked a simple question, “Have you considered whether the anti-vax information you have is a Chinese and Russian disinformation campaign designed to weaken the United States’ populace?” She experienced a mind-blown moment. He said after that she came with all of her children ever single time right on the vax schedule….

Please note this doctor DID NOT ADDRESS the core problem — the perceived dangers of vaccines — Instead he substituted one FEAR for another FEAR.

So let’s back-up and ask the questions that doctor did not address.
WHY would the woman have:

#1. Distrust in the US government
#2. Distrust in the pharmaceutical companies
#3. Does her fear have a solid foundation?

Unfortunately, as we have seen over the last seven decades, the US government IS the Enemy of the American People. (see Codevilla’s article linked above) So the woman’s ‘Fear’ of the intentions of the US Government has a solid foundation. She can not trust that the government has HER best interests and NOT the best interests of the vaccine manufactures at heart when decisions are made.

Second US Scientists and drug companies are NOT to be trusted and neither is the FDA. I have a whole file folder on Fake Research and Data falsification. Here is a tiny sample germane to a discussion on vaccines:
US Scientists Significantly More Likely to Publish Fake Research, Study Finds

PLoS ONE: How Many Scientists Fabricate and Falsify Reseach? A Systematic Review <<<VERY GOOD!

PLoS Medicine: Why Most Published Research Findings Are False

Science Mag: Peer Review is Sick and Collapsing Under it’s Own Weight

Scientific Fraud and the Power Structure of Science

Research Misconduct Identified by the US Food and Drug Administration: Out of Sight, Out of Mind, Out of the Peer-Reviewed Literature

….Results
Fifty-seven published clinical trials were identified for which an FDA inspection of a trial site had found significant evidence of 1 or more of the following problems: falsification or submission of false information, 22 trials (39%); problems with adverse events reporting, 14 trials (25%); protocol violations, 42 trials (74%); inadequate or inaccurate recordkeeping, 35 trials (61%); failure to protect the safety of patients and/or issues with oversight or informed consent, 30 trials (53%); and violations not otherwise categorized, 20 trials (35%). Only 3 of the 78 publications (4%) that resulted from trials in which the FDA found significant violations mentioned the objectionable conditions or practices found during the inspection. No corrections, retractions, expressions of concern, or other comments acknowledging the key issues identified by the inspection were subsequently published.
Conclusions and Relevance
When the FDA finds significant departures from good clinical practice, those findings are seldom reflected in the peer-reviewed literature, even when there is evidence of data fabrication or other forms of research misconduct….

The FDA did manage to catch one… FDA says CRO Cetero faked trial data; pharmas may need to redo tests

NEWS ARTICLES
NYT: Rise in Scientific Journal Retractions Prompts Calls For Reform

Daily Mail UK: The ‘false’ pandemic: Drug firms cashed in on scare over swine flu, claims Euro health chief

Word Press CENSORED this site, Live Avian Flu Virus Placed in Baxter Vaccine Materials Sent to 18 Countries

The company that released contaminated flu virus material from a plant in Austria confirmed Friday that the experimental product contained live H5N1 avian flu viruses….
On Friday, the company’s director of global bioscience communications confirmed what scientists have suspected. “It was live,” Christopher Bona said in an email.
The contaminated product, which Baxter calls “experimental virus material,” was made at the Orth-Donau research facility. Baxter makes its flu vaccine — including a human H5N1 vaccine for which a licence is expected shortly — at a facility in the Czech Republic.
People familiar with biosecurity rules are dismayed by evidence that human H3N2 and avian H5N1 viruses somehow co-mingled in the Orth-Donau facility. That is a dangerous practice that should not be allowed to happen, a number of experts insisted. Accidental release of a mixture of live H5N1 and H3N2 viruses could have resulted in dire consequences….

Alternate from Physicians for Life: (Not a Word press blog) Live Avian Flu Virus Placed in Baxter Vaccine Materials Sent to 18 Countries (2009)

I remember when this information hit the news and I was appalled. I have worked as a QC Engineer in Drug manufacture. There is NO WAY IN HADES this should have happened. WHY? Because you LABEL EVERYTHING and it is double signed off when raw materials are withdrawn from the warehouse by manufacturing to PREVENT this type of mistake.

Vaccine Industry Watchdog Obtains CDC Documents That Show Statistically Significant Risks of Autism Associated with Vaccine Preservative Thimerosal

“Biochemist Brian Hooker, scientific advisor to A Shot of Truth, reveals CDC knew of risks for over a decade.”

February 19, 2014
For nearly ten years, Brian Hooker has been requesting documents that are kept under tight wraps by the Centers for Disease Control and Prevention (CDC). His more than 100 Freedom of Information Act (FOIA) requests have resulted in copious evidence that the vaccine preservative Thimerosal, which is still used in the flu shot that is administered to pregnant women and infants, can cause autism and other neurodevelopmental disorders.
Dr. Hooker, a PhD scientist, worked with two members of Congress to craft the letter to the CDC that recently resulted in his obtaining long-awaited data from the CDC, the significance of which is historic. According to Hooker, the data on over 400,000 infants born between 1991 and 1997, which was analyzed by CDC epidemiologist Thomas Verstraeten, MD, “proves unequivocally that in 2000, CDC officials were informed internally of the very high risk of autism, non-organic sleep disorder and speech disorder associated with Thimerosal exposure.”….

http://jonrappoport.wordpress.com/2014/08/26/cdc-whistleblower-is-just-the-tip-of-the-iceberg/“>CDC whistleblower is just the tip of the iceberg

…“It is simply no longer possible to believe much of the clinical research that is published, or to rely on the judgment of trusted physicians or authoritative medical guidelines. I take no pleasure in this conclusion, which I reached slowly and reluctantly over my two decades as an editor of The New England Journal of Medicine.” —(Marcia Angell, MD, “Drug Companies and Doctors: A story of Corruption.” NY Review of Books, Jan. 15, 2009.)
Here is another quote of a similar nature, also published in the NY Review of Books (May 12, 2001, Helen Epstein, “Flu Warning: Beware of Drug Companies”):
“Six years ago, John Ioannidis, a professor of epidemiology at the University of Ioannina School of Medicine in Greece, found that nearly half of published articles in scientific journals contained findings that were false.”…

So I hope these articles establish the fact this woman had a solid foundation for her concerns and the doctor’s default to ‘BLAME IT ON RUSSIA’ would be funny if it was not so serious.

Do you really think these Mega-corporations, who PAY the doctors, ACTUALLY CARE if a certain percentage of children are crippled or die from their vaccines? Don’t you think the Elite would LIKE to see American girls made sterile and more people on the government dole to aid the Cloward–Piven strategy?

What the Mega-corporations care about is MONEY and they have that all fixed up.

1987 ‘Limited’ Liability LAW:
42 U.S. Code § 300aa–22 – Standards of responsibility

….No vaccine manufacturer shall be liable in a civil action for damages arising from a vaccine-related injury or death associated with the administration of a vaccine after October 1, 1988, solely due to the manufacturer’s failure to provide direct warnings to the injured party (or the injured party’s legal representative) of the potential dangers resulting from the administration of the vaccine manufactured by the manufacturer….

“Vaccine makers and federal officials will be immune from lawsuits that result from any new swine flu vaccine, under a document signed by Secretary of Health and Human Services Kathleen Sebelius, government health officials said Friday.”
http://www.google.com/hostednews/ap/article/ALeqM5hjdCHrP82YTFser5vD6CzTK1az6wD99GH8580

The first doses of swine flu vaccine will be given to the public before full data on its safety and effectiveness become available, doctors confirmed yesterday…..But, unlike seasonal flu vaccine, the pandemic version will be spread over two doses in a higher quantity, and one brand is expected to contain a chemical additive to make it go further, potentially increasing the risk of side-effects.http://www.independent.co.uk/life-style/health-and-families/health-news/safety-questions-over-swine-flu-jab-1751547.html

“On February 22, 2011 the U.S. Supreme Court shielded drug companies from all liability for harm caused by vaccines mandated by governmentwhen companies could have made a safer vaccine…. From now on, drug companies selling vaccines in America will not be held accountable…
The only difference is that three decades ago, government officials were ordering doctors to give children 23 doses of 7 vaccines and, today, that direct order is up to 70 doses of 16 vaccines.” NVIC link

Since this law has been upheld in the Supreme Court, WE the consumers now get to PAY for those crippled or killed:
Vaccine injury compensation programs:
https://www.historyofvaccines.org/content/articles/vaccine-injury-compensation-programs

Other sites discussing vaccines:
http://www.financialsensearchive.com/editorials/engdahl/2010/0304.html

http://www.whale.to/vaccines/horowitz4.html

OK Time to leave the politics of vaccines and actually take a look at vaccination.

Here is the US Vaccination schedule for children.

https://www.cdc.gov/vaccines/schedules/hcp/imz/child-adolescent.html#vaccines-schedule

[Wolfie can you include a screen shot of the chart for Birth to 15 Months please?]

Here you go!
Wolf

First I am NOT a doctor and I do not have human kids. Mine are goats kids and lambs. However we are all mammals so at least some information applies across species.

Starting with newborns:
Colostrum definition: A sticky white or yellow fluid secreted by the mammary glands after giving birth, rich in antibodies. The antibodies absorbed by the newborn protect against systemic invasion by pathogens while antibodies that are not absorbed play an important role in protection against intestinal disease.

The small intestine is lined with immature cells which are capable of absorbing macromolecules.
Immunoglobulins ( antibodies) can not transmission across the placenta of the mother to the fetus. Instead the Immunoglobulins in the Colostrum is absorbed in the small intestine and thereafter transported to the blood. “The absorption of immunoglobulins has dropped to a relatively low level after 24-36 hours.” — The importance of colostral immunoglobulins and their absorption from the intestine of the newborn animalsfrom the National Center for Biotechnology Information, U.S. National Library of Medicine

Vaccination: Kid goats that had passive immunity from immunized dams, don’t get their CD/T vaccination until 8 weeks and again at 11-12 weeks. My vet doesn’t recommend doing it earlier. HOWEVER If the kid didn’t receive its mom’s colostrum or if the doe didn’t get vaccination a month or so before birth, you should vaccinate the kid at the age of 1 to 3 weeks and again three to four weeks later. (And PRAY)

Sheep 201: Flock vaccinations written by Susan Schoenian, Sheep & Goat Specialist at the University of Maryland’s Western Maryland Research & Education Center in Keedysville, Maryland.

…
Passive immunity
Vaccines are not very successful in young lambs, 1-2 months of age. For this reason, vaccination strategies recommend vaccinating pregant ewe to confer passive immunity to the lambs through the colostrum (dam’s first milk). Ewes should be vaccinated with the CDT toxoid approximately 4 weeks prior to lambing. Ewes lambing for the first time will need to be vaccinated twice in late pregnancy, four weeks apart. Maternal antibodies will protect lambs for six to eight weeks so long as lambs consumed adequate amounts of colostrum. It is recommended that a lamb consume 10 percent of its body weight in colostrum.
Lambs
Lambs should receive their first clostridal vaccination when they are approximately 6 to 8 weeks of age, followed by a booster 4 weeks later. If pastured animals are later brought into confinement or dry lot for concentrate feeding, a third vaccination should be given. Some experts recommended giving artifically-reared lambs multiple vaccinations.
Lambs whose dams were not vaccinated for C and D can be vaccinated with some success at two to three days of age and again in two weeks. However, later vaccinations will likely be more effective, as colostral antibodies usually interfere with vaccinations at very young ages. The lamb’s immature immune system may also not be able to respond to vaccination at such a young age.

Lambs and goats are usually weaned at 2 to 3 months, horses at 4 to 6 months. Lambs and goats live to mid teens, horses into there 20s and 30s. Human babies are weaned naturally sometime between 2 and 4 years of age. Humans live into their 70s and 80s. Animals are usually vaccinated AFTER they are weaned!

Last recommendation: ” Each producer must weights the pros and cons of vaccinating for a specific disease. If the cost of vaccination exceeds the expected losses, then vaccination is probably not cost-effective….The risk of a diseases outbreak should be the criteria that is used to determine the need for vaccination.” — Susan Schoenian, Sheep & Goat Specialist
Translation: Check with your vet/ vet school on what diseases are around your area and ALWAYS limit the exposure of your animals. If you show have separate quarantine areas for show animals also for animals you are newly introducing to the farm.
…

What is the take home from all of this?
1. QUARRANTINE IMMIGRANTS don’t bring the disease into the country in the first place. Since our traitorous government refuses to do this, do as much as you can to limit your exposure and your children’s exposure especially for the very young. (I hate seeing infants at a daycare as I did yesterday.)

2. MOM should receive the vaccinations not the New Born.

3. MOM should breast feed during the first few days to pass immunity to her baby even if she does not plan to continue breastfeeding. Try to stay home with your infant or use a private individual (like grand parent) for your very young baby instead of a commercial daycare. This limits disease exposure and thus need for very early vaccination.

4. Infant vaccination is a poor second for nature’s Colostrum and very early vaccination is needed only if Mom has not past immunity on to the infant via Colostrum AND can not manage quarantine conditions. (Why my bottle lambs were in the kitchen and are even now in a quarantined area instead of with the sheep.)

I have also been warned by my vet that the vaccines for multiple diseases are not a smart idea. Spacing the vaccinations of individual diseases works MUCH better.

Seems President Trump agrees!

H/T to thinkthinkthink who on April 30, 2019 at 20:55 Said:

PDJT had strong opinions on timing of vax shots for his children, just as these parents did.

https://pbs.twimg.com/media/D5RkmLsXoAE4kle.jpg

There you have it. Please feel free to comment in any way you see fit. WE – unlike everybody else in socialist media – have free speech. Moreover, it is not MY JOB to determine what is “misinformation”. That is YOUR JOB.

**FREE AS IN THE FREE FALL OF THE SOCIALIST MEDIA AND FAKE NEWS INTO A TRAP OF THEIR OWN CONSTRUCTION**

AND Logic: The Conspiracy to Ban Guns

by Gail Combs

title and foreword by Wolf Moon

I have often harped on the idea that the left – and enemies of truth in general – have managed to sneak a considerable amount by us, by using a very generalized kind of disinformation. Rather than corrupting our DATA – our facts – they have actually managed to corrupt our THINKING – our processing of the data. This is a far more powerful and insidious way of dominating us.
Small facts can be hidden by small lies. Huge conspiracies can be hidden by small changes to our thinking.
One of the chief ways this has been done, is by subconsciously promoting the simplistic approach of “either-or” thinking – namely XOR (“exclusive OR”) logic. There is a HUGE difference between XOR and OR, because OR logic includes the case or cases where two or more options are simultaneously true – namely AND logic.
XOR thinking is promoted by many means which appear to have nothing at all to do with it. For example, by simply lowering the quality of discourse from calm inquiry to heated argument, XOR thinking is advanced, and more nuanced AND logic is thrown out the window. Thus, TROLLING is a very effective way to advance XOR logic as a means to HIDE TRUTH.
When I talk about the promotion of XOR logic, I’m frequently talking about non-interacting alternatives, where one idea is HIDDEN from investigation, by simply advancing shinier and easier-to-believe alternatives. This works nicely with Eckert’s Law (regarding the thwarting of Occam’s razor by deception), because DECEPTION allows us to construct unbelievable alternatives as realities, and then protect them from scrutiny by means such as simpler and more plausible chaff alternatives. MILITARY CAMOUFLAGE and INSECT MIMICRY both work on this principle. These are both the work of INTELLIGENCE – in one case neural individual intelligence, in the other case distributed evolutionary intelligence.
Now – here is an interesting thought which Gail Combs had – something which not only breaks down such forms of deception, but helps us to see the bigger picture.
What if AND logic doesn’t just bring a hidden alternative back into play for some cases, but actually explains the TOTALITY of facts BETTER than either explanation alone? What if there is EXPLANATORY SYNERGY? In essence, we are recovering a LARGER AND BETTER ruling by Occam’s razor from not just a more LIMITED ruling, but a more MISTAKEN one.
This is something we should add to our logic arsenal. TWO explanations , or a single larger one, may not simply explain MORE cases. Two explanations, or a single larger one, may actually explain all individual cases BETTER.
When we find such a condition, we need to ADVANCE THE BETTER, LARGER EXPLANATION. And we need to fight back against oversimplifying opposition, like the fake news media, which demands compactness and simplicity NOT when it suits the discovery of larger and greater truth, but rather when it suits their agenda of deception.
NOW – on to the specific case under discussion.
What Gail is presenting here is not merely a perfect example of “finding a better, larger, combined explanation”. This is much bigger.
This thinking actually offers the first really good explanation of what I would call the COMPLETE PICTURE of Eric Holder’s greatest wish:
“a way to brainwash people against guns”.
This post explains how numerous curious Democrat strategies are actually connected by a single larger purpose which explains them all. To be really, really blunt about it:
“a way to MK people against guns”.
What we have RIGHT HERE is one of the GRANDEST uses of MK in history – at all levels from targeted individual to mass global. We can now EXPLAIN many Democrat actions which seemed to lack any coherent purpose.
Oh, no. These actions had a purpose. And when we have elucidated the complete, monstrous, THEORY and EXPLANATION of the entire operation, Eric Holder needs to be confronted with every single facet in a court of law, so we can know the TRUTH.
Wolf Moon

PART ONE: Introduction

I am going to start with the information from Wolfmoon that triggered my new thoughts and expanded my thinking to “AND LOGIC.“ . The following quotes are from his Déjà Woo and The Unbelievable Convenience of Amnesia articles plus his comments within those articles.

As Wolfmoon says: “This is a perfect place to practice AND LOGIC.“ I have always thought of it as multidimensional thinking instead of linear thinking.

An example of AND LOGIC. is:

Smoking [PLUS] Asbestos = Lung Cancer.

It takes BOTH to get a high incidence of lung cancer but the activists, lawyers and MSM ignored the actual evidence and blamed only Asbestos.

Most people look for the simple logic of If = Then. They do not consider the more complicated If #1 [PLUS] #2 [PLUS] #3 = Then. or as Wolfmoon put it “AND LOGIC.”

The FIRST BIG CLUE from Wolfmoon:

“People will also start looking for MK where it is actually most common and most useful – where it MAKES MONEY and GRABS POWER for DEMOCRATS.”

…POWER…. Hmmm.

A great example of this is the Global Warming Scam. HUGE amounts of tax payer $$$ have been diverted into the pockets of select individuals. For example:

“Nancy Pelosi’s brother-in-law is given $737m of taxpayers’ money to build giant solar power plant in middle of the desert. Obama administration approved $1 billion in green energy loans days after failed Solyndra project due to be completed. Energy Department is ‘rushing’ $5bn in loans ahead of Friday deadline.” link

The SECOND BIG CLUE from Wolfmoon:

“….PTSD, anybody? Think about it. AUTOMATIC COVER. And not just that. Supposedly these [MK] techniques work better in the AFTERMATH of traumatic events….”

Would these techniques work even better on a person who has been given BRAIN ALTERING drugs since they entered grade school? Would the power hungry do that to millions of American children in their quest for more and more power?

The THIRD BIG CLUE from Wolfmoon:
This is the real KEY:

“….People cannot even comprehend this idea of making people do something highly non-sensical and possibly even self-destructive…. They have been programmed by Fake Entertainment to reject this stuff as entirely fictional, or sufficiently fictional that it is no more than a parlor trick.
Nobody will tell them about the mathematics of low wins on high purses – the idea that if 9 out of 10 low-level money-maker MK ops fail, but one wins, it EASILY pays for the failures. Americans have been conditioned to believe that only highly reliable techniques are ever deployed. People fail to understand that failure is an accepted part of statistical wins.
My prejudices about what is possible in mind control are why for YEARS I never picked up on a person who did something highly nonsensical that resulted in the goals of CA3 [Conspiracy to Advance Affirmative Action] being fulfilled….
…Spycraft, mission enhancement, obfuscation and disinformation are part of it. Accident creation, crime enabling, and violence are the rest….
Are you starting to see why “MK” and “crazy” go together? Think like a CRIMINAL to see how it’s used. Think like a HACKER who does not want to get caught. Understand WHY discreditation is used to PROTECT technology…”

Wolfmoon was looking at a Conspiracy to Advance Affirmative Action. I am looking at the big one, The Conspiracy to Advance a Complete Gun Ban.

PART TWO: Power grab

The FIRST BIG CLUE from Wolfmoon:
“GRABS POWER for DEMOCRATS.”

What is the BIGGEST stumbling block keeping the Communists, masquerading as Democrats, from grabing complete control of the USA and thus the world? Our Second Amendment rights to own weapons!

Our founding fathers knew exactly how important an armed citizenry was to the preservation of freedom.

https://i.pinimg.com/originals/72/36/47/723647394503dc68c850adb03224017d.jpg

Firearms stand next in importance to the Constitution itself. They are the American people’s liberty teeth and keystone under independence.
George Washington

History teaches us gun control is the first step of the totalitarian dictator. Murder of defiant subjects is the second:

1911 Turkey Gun control — from 1915 to 1917 – 1.5 million Arminans killed
1935 China gun control — from 1948 to 1952 – 20 million killed
1938 Germany Gun control — from 1935 to 1945 – 20,946,000 murdered.
1956 Cambodia gun control — from 1975 to 1977 – 1 to 2 million educated people murdered.
1964 Guatamala Gun Control — from 1964 to 1981 – 100,000 Mayan Indians killed.
1970 Uganda gun control in — from 1971 to 1979 – 300,000 Christians killed, a total of 2 to 3 million murdered.

http://www.quotesvalley.com/images/61/political-power-grows-out-of-the-barrel-of-a-gun.png

PART THREE: Change the Conversation and hide the evidence.

Americans are NOT about to give up their guns. This is especially true of Conservatives, who understand our Second Amendment rights are about preserving our freedom and our Constitution. They understand gun rights are NOT about hunting or self defense. For years the Left has been trying to change the conversation and hide WHY gun ownership is a RIGHT and not a government granted privilege. It hasn’t worked well. Now they realize to grab our guns, they must paint Conservatives as ‘VIOLENT Right-Wing Extremists’ so the arguments by Conservatives will be discounted. The goal is not just to have the arguments of the Conservatives discounted, but to make people FEAR Conservatives so there will be no shock, only relief when these ‘VIOLENT Right-Wing Extremists’ are slated for ‘re-education’ or extermination.

First paint the opposition as the devil incarnate, then take them out. After all the technique work very well for the Nazis and the Soviets and other totalitarian regimes. Why argue with success?
…

It wasn’t until I was doing the research for this article that I realize the implications of what I had seen on Election day, 2018. A friend and I, wearing Trump/Pence 2020 T-shirts, were handing out flyers at our local polling place. I am close to 70 and under 5′ 4″ while my friend was a short male, perhaps 5’6″. We were talking with a couple of Democrat ladies who were over 50, when a woman in her twenties came towards us. She stopped short, stared at us, and made a wide circle around us. She was clearly SCARED TO DEATH of us!! http://www.sherv.net/scratching.head-emoticon-5921.html

This young lady was an example of just how well the propaganda about ‘VIOLENT Right-Wing Extremists’ was working.

Wolfmoon: “…Like I always say, 99.99(numbers)% of MK is done openly – mostly by the Mind Control Media, but also by individually tailored psy-ops through social media….” This young woman was a perfect example of a victim of the Mind Control Media’s psy-ops. She acted as if she truly believed we would actually get violent and hurt her!

Since the goal of the Left is to paint Conservatives as THE ENEMY and the only enemy, the last thing they want is a competing narrative out there. Therefore, ever since 9/11 the Left has been trying to shift the narrative from Islamic Terrorists to Homegrown Extremists’ aka VIOLENT Right-Wing Extremists.

Here are news stories that show the slow morphing of the focus and the narrative.

First step – shutdown Department of Homeland Security targeting of the REAL Terrorists:
After all you can not have the Sheeple realize you are importing Islamic Terrorists into the country by the bus load.

SYNOPSES of Breitbart Article:
Department of Homeland Security whistleblower Philip Haney, was a founding member of the Passenger Analysis Unit,(PAU). It was established as a stand-alone agency in 2003 after 9/11. He was moved to the National Targeting Center and tracked Tablighi Jamaat, a Salafist Muslim fundamentalist group. Haney discovered a large number of Tablighi Jamaat members were entering the United States on the visa waiver programs often on E.U. – UK passports. They were proceeding to locations known to be part of the extremist networks in the USA Haney had been piecing together. Haney and his fellow investigators found links from the Tablighi Jamaat network to Hamas, al-Qaeda,and global terrorist funding. But his initiative was deemed politically incorrect under the Obama Admin. and shut down by the Department of Homeland Security’s Civil Rights and Civil Liberties division. — link
Even Politico talks of The secret backstory of how Obama let Hezbollah off the hook “…the Obama administration derailed an ambitious law enforcement campaign targeting drug trafficking by the Iranian-backed terrorist group Hezbollah, even as it was funneling cocaine into the United States… Hezbollah turned to trafficking cocaine and laundering money through used cars to finance its expansion.”

Meanwhile the media continues to bury the evidence linking any shootings TO Jihad. Unless the person is a White Conservative and/or Christian, color, nationality and religion are left out of the news stories. In one case the Judge even blocked the prosecutors from using evidence to explain the motive of the Fort Hood shooter!

Next STEP – Start shifting the blame

Napolitano stands by controversial report

April 16, 2009
“Homeland Security Secretary Janet Napolitano said Wednesday that she was briefed before the release of a controversial intelligence assessment and that she stands by the report, which lists returning veterans among terrorist risks to the U.S…..”
https://www.washingtontimes.com/news/2009/apr/16/napolitano-stands-rightwing-extremism/?page=all

The actual report? Rightwing Extremism: Current Economic and Political Climate Fueling Resurgence in Radicalization and Recruitment

Note the phrases: “Threats from white supremacist and violent antigovernment groups during 2009 have been largely rhetorical and have not indicated plans to carry out violent acts.” because you will see them again in the January 18th, 2018 Politifact article where the term Far-right extremist groups “include white supremacists and anti-government militias, among others.”

It is worth at least skimming that report because it hits on many of our concerns, NAFTA, China, “Proposed imposition of firearms restrictions and weapons bans …
…the perceived loss of U.S. jobs in the manufacturing and construction sectors, and home foreclosures. … extremists attribute these losses to a deliberate conspiracy conducted by a cabal of …“financial elites.”
…the perception that illegal immigrants were taking away American jobs through their willingness to work at significantly lower wages….” (After all those concerns are all in our heads and not real right?)

Napolitano: terror threat may be highest since 9/11

February 9, 2011
Washington (CNN) — The terrorist threat to the U.S. homeland has continued to “evolve” and may now “be at its most heightened state” since the September 11, 2001, terror attacks, Homeland Security Secretary Janet Napolitano told members of Congress on Wednesday.
There is an increased reliance on recruiting Westerners into terrorist organizations, she told the House Homeland Security Committee. State and local law enforcement officers are increasingly needed to combat terror, and the focus must be on aiding law enforcement to help them secure communities, she said….
http://www.cnn.com/2011/US/02/09/terror.threat/index.html?hpt=T2

LAST STEP — Show Muslims are NOT terrorist risks, but that VIOLENT Right-Wing Extremists ARE!!!

November 7, 2018 one day after elections there was a shooting that made the headlines.

Given Wolfmoon is correct and the Deep State can orchestrate some of these shooting, I think the TIMING of this shooting was off. Perhaps the guy was strong enough to fight the ‘directive’ for a few weeks. I think it was supposed to occur a week or more BEFORE the elections and be another “George Zimmerman – Trayvon Martin” media circus to drive voters TO the Democrat candidates. However it is interesting to read what was written, to see the MK Psy-ops embedded in the story because it sticks out like a sore thumb.

The story is not just about an unfortunate shooting, it is all about BLAME CASTING. The story echoes the same type of blame casting seen in the Zimmerman – Martin media circus. In that previous case the media was banging the drum about a ‘White on Black’ crime;. Or as Wolfmoon put it the Conspiracy to Advance Affirmative Action, and stir up blacks to vote for Obama.

Note it also falls right in with Wolfmoon’s proposal: “….PTSD, anybody? Think about it. AUTOMATIC COVER. And not just that. Supposedly these [MK] techniques work better in the AFTERMATH of traumatic events….”

The Left Narrative Engineering from Fortune Magazine:

Last night, a gunman opened fire in the Borderline Bar and Grill last night in Thousand Oaks, Calif. At least twelve people are dead, including Ventura County Sheriff Sgt. Ron Helus, and up to fifteen more were injured.
The shooter was Ian David Long, and he was a Marine Corps veteran. He was found dead at the scene. He seemed deeply troubled…..[As Wolfmoon said, very useful to have a killer, with PTSD, who ends up dead as cover. Almost all of these shooters end up dead because dead men can’t talk.]
we’re in a period of time when this kind of mass violence fails to shock for very long…. And a meaningful political conversation about guns, one that reflects the true concerns of all constituents…
But we’re also in a period where hate speech and the violence it inspires has been on the rise. [ Yea Think?Breitbart Rap Sheet: ***639*** Acts of Media-Approved Violence and Harassment Against Trump Supporters ]
Here’s one data point. White supremacists and other far-right extremists have killed far more people in the US since Sept. 11, 2001, than any other type of extremist group. By far. According to the Anti-Defamation League, some 71 percent of the extremist-related fatalities in the United States between 2008 and 2017 were committed by members of the far right or white-supremacist movements, compared to just 26 percent committed by people associated with Muslim groups.
And yet, official counter-terrorism efforts focus only on potential “jihadists” and not on the white supremacists who are now organizing in similar ways.….
“We’re actually seeing all the same phenomena of what was happening with groups like ISIS, same tactics, but no one talks about it because it’s far-right extremism,” P. W. Singer, a national-security strategist with the New America think tank tells Janet Reitman in a deeply reported piece for The New York Times. Even before the Trump administration, he says, “we willingly turned the other way on white supremacy because there were real political costs to talking about white supremacy.”….. http://fortune.com/2018/11/08/raceahead-california-shooting/“

BOY, they sure are cranking up the volume!

Fartacus [Cory Booker] also jumps in and keep the new narrative in the limelight…

“In American history since 9/11, we’ve had 85 major attacks in our country, 73 percent of them have been by white nationalist hate groups.” — Cory Booker on Tuesday, January 16th, 2018 in an interview on CNN

Of course you have to have the ‘Controlled Opposition’ chime in to MUDDY THE WATERS to keep the Sheeple from thinking for themselves. The key is to tone it down some but still leave the impression ‘far-right extremist groups’ are numerous and dangerous.

Polifact on the Booker quote:

Among those incidents, far-right violent extremist groups were responsible for 62 incidents (73 percent) while radical Islamist violent extremists were responsible for 23 incidents (27 percent).
Booker used the term “white nationalists,” but that’s not exactly the same thing as far-right extremist groups….
The GAO report (see page 29) shows that a subset of far-right incidents — about 38 incidents — were committed specifically by white supremacists…. https://www.politifact.com/truth-o-meter/statements/2018/jan/18/cory-booker/fact-checking-cory-bookers-statistic-attacks-white/

Cory Booker Uses Misleading Terror Data To Attack Trump — Daily Caller
WELLlll, they got it part right at least.

“…One of the particular points of contention for Booker was how the White House allegedly ignores America’s white supremacists, whom the senator argued were more dangerous than Islamic militants….
In Booker’s dramatic monologue, he claimed that all of these attackers held “bigoted, hateful ideas about minorities” and implied he wanted 73 percent of the DHS’s time spent tracking down these far-right extremists.
However, there are serious issues with the GAO report that Booker used to argue white supremacists are the biggest terror threat to the nation. One of the major problems with the study is what incidents it lumps in with right-wing terror.
The biggest error in GAO’s data on white supremacist terror was caught by National Review’s David French last April. The Umpqua Community College shooting, one of the deadliest shootings the GAO attributed to a white supremacist, was actually committed by an African-American with no discernible ideology outside of hatred for religion.
Anti-government activists who appeared not to have been motivated by hate for minorities committed a good portion of the violent incidents the study categorized as right wing terror — contrary to what Booker argued on Tuesday. The GAO study also includes prison slayings carried out by white supremacist gangs as cases of domestic terror.
Another problem French found with the study was its glaring omission of left-wing terrorism….. https://dailycaller.com/2018/01/17/cory-booker-trump-gao-report/

Of course BOTH articles blow it, leaving the basic impression behind that there ARE far-right violent extremist groups who are more of a problem than muslim jihadists just as the Deep State planned.

So what is the truth? After all we need the truth to counter the Media’s Psy-ops.

PART FOUR: Lie with Statistics

The Left LOVES to lie using false statistics or fudged numbers. With luck I do not mess up my math. So here goes.

The problem with the narrative that far-right extremists are more dangerous than radical Islamist extremists is it does not take into account population or to be more precise incidence per 1,000,000 people.

Scrounging around the internet I found these numbers:

The US Population is ~ 327 million.
The White, non-Hispanic or Latino population make up 61.3% of the nation’s total, with the total White population (including White Hispanics and Latinos) being 76.9%. — WIKI

65 percent whites leaned right in 2016 per a Washington Compost article by Joshua N. Zingher, an assistant professor of political science at Old Dominion University.

Calculating the white, non-Hispanic, population:
61.3% of 327 million is 200 million

And if you want to get picky, and count only the right-leaners:
65% of 200 million is 130 million

A Pew estimate of Muslims in 2017 is that they are about 1.1% of the total U.S. population. A Pew Forum report on American religion found that Muslims accounted for 0.9% of American adults in 2014, up from 0.4% in 2007, due largely to immigration. (Wikipedia) Note that during the BHO administration the population of Muslims more than doubled.

1.1% of 327 million is 3.6 million
…..

So what are the number of incidents per million people?

There were 62 incidents, assuming that those are by white right-wing people, and NOT ANTIFA or Anarchists, whom we may call white Commies.

Total White Population
62 divided by 200 million = 0.31 incidence per million

(or the picky number)
62 divided by 130 million = or 0.48 incidence per million

23 incidents by radical Islamist extremists
23 divided by 3.6 million = 6.4 incidence per million. That’s 20 TIMES THE RATE.

So Fartacus is Farting PURE Pig feces yet again!

But that leaves the real question. HOW do you GET ‘VIOLENT Right-Wing Extremists’ in the first place, when Conservatives are generally more peaceful and law abiding than the Left???

PART FIVE: Producing VIOLENT Right-Wing Extremists.

This is where WolfMoon’s insight and experience comes into play and the light bulb went off in my head.

“Nobody will tell them about the mathematics of low wins on high purses – the idea that if 9 out of 10 low-level money-maker MK ops fail, but one wins, it EASILY pays for the failures. Americans have been conditioned to believe that only highly reliable techniques are ever deployed. People fail to understand that failure is an accepted part of statistical wins.”

With the media providing cover and a corrupt government fudging the statistics, all you need is to INCREASE VIOLENCE among white males and then place the selected stories all over the news.

But HOW do you increase violence? DRUGS! Not only street drugs but carefully selected drugs administered TO the target —>WHITE MEN<—… or the little boys who will grow up to be white men.

They KNEW the drugs they are forcing on school children would turn them violent. THEY KNEW DECADES AGO!

..in 1973, psychiatrists were giving amphetamines to volunteers in order to observe their reactions. The reactions frightened researchers, who noted that several of the subjects expressed “a desire to kill” or to do something “bad or destructive.”….” (This and the following quotes are sourced in my “Thursday comment” mentioned below.)

So they came up with a ‘new disease’

“…it was not until the late 1960s that the American Psychiatric Association (APA) formally recognized ADHD as a mental disorder….”

Prior to that, in 1957 Laufer et al….“found that “children with the hyperkinetic impulse disorder… had a lower threshold for clinical responses in EEG to the administration of metrazol than children without the hyperkinetic syndrome. Following the administration of amphetamines, however, the threshold was similar to that of children without evidence of the syndrome…”

If you want the history: *https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000907/

So now you have a reason to administer amphetamines to school children without an evidence of even ‘minimal brain damage’

PART SIX: Next step is to make sure the Kids HAVE THE SYMPTOMS!

Well that is easy:

1. NO discipline is pushed: The Hand that Rocked the Cradle: A Critical Analysis of Rockefeller Philanthropic Funding, 1920-1960

2. Mom is pushed out of the house via Feminism: How The Rockefellers Re-Engineered Women

3. Change the diet to a high carb, high sugar diet and put candy and soda machines in the schools.

4. REMOVE EXERCISE

You should see my lambs when I let them out of the dog crate in the morning. They buck and kick and run and jump… And yet we expect to CAGE little children, ESPECIALLY BOYS all day long in daycare or school without them rebelling?

And when they do we call it a ‘mental problem?
And people swallow this?
Are you effing kidding me??
…

There are 73.7 million children in the USA. And According to the CDC “More than 5 in 10 children (53.5%) aged 3-17 years with behavior disorders received treatment.” AGE THREE???
*https://www.cdc.gov/childrensmentalhealth/data.html

This is a short summary of my Thursday Comment It included the links for the following quotes.

“In 1996, 10 percent to 12 percent of all American schoolboys were taking the addictive Ritalin.”

“A study released this month by the National Center on Addiction and Substance Abuse at Columbia found that the number of teenagers who admit to abusing prescription medications tripled from 1992 to 2003, while in the general population such abuse had doubled”

“…Among elementary students, 17% of all students and 33% of white boys had been diagnosed with ADHD and the vast majority had been medicated for this condition at some time during the 1997-98 school year…. Ninety percent of all identified cases had been medicated for the disorder at some point …”

Think that is bad? It gets WORSE!

“… These findings suggest that as of 1998, school-based studies of ADHD prevalence captured approximately half of the cases treated in the community. Preliminary data from a follow-up study suggest that as of 2002, school records capture as few as 25% of ADHD cases (LeFever, 2002)….”

RITALIN AND VIOLENCE

… there are now over 5 million school kids in America on psychotropic drugs, most of which are prescribed and administered by the schools themselves. ….December 1996, there are four million kids on Ritalin alone, one of the most powerful of the drugs now being given routinely to children in American schools.

What is most disturbing, however, is the growing awareness that the increased violence among school children may have more to do with the drugs than with the guns they use to carry out their violence. ”’

NO Sh…T You think??

So there you have Wolfmoon’s “low-level money-maker MK ops” They only need 0.0001% of the White boys they mess up to go violent. The added benefit is it is the mostly highly intelligent ALPHA males who are likely to rebel and have their brains permanently messed up. A real Win-Win.

So you have the stage set.

There are 73.7 million children in the USA, 14.7 million are boys and about 1/2 are white or ~7 million. If 10% to 33% are drugged, that is at least 7,00,000 to 2,310,000 possible ticking time bombs. Even if only 1 in 10,000 go violent you have 70 or more artificially created incidents.

Remember Booker is citing a GAO Report about incidences from from Sept. 12, 2001 — the day after the 9/11 terror attacks — through Dec. 31, 2016, or fifteen years. “In 1996, 10 percent to 12 percent of all American schoolboys were taking the addictive Ritalin.” So plenty of time for those boys to grow up and kill people…

…. there are now over 5 million school kids in America on psychotropic drugs, most of which are prescribed and administered by the schools themselves. ….December 1996, there are four million kids on Ritalin alone, one of the most powerful of the drugs now being given routinely to children in American schools.
What is most disturbing, however, is the growing awareness that the increased violence among school children may have more to do with the drugs than with the guns they use to carry out their violence.
…Eric Harris, 18, who, with his friend Dylan Klebold, murdered his fellow students at Columbine, had been taking Luvox, one of the new antidepressant drugs approved in 1997 by the Food and Drug Administration for treatment of obsessive-compulsive disorder, or OCD, among children under 18.
…. T. J. Solomon, 15, who shot and wounded six classmates at Heritage High School in Conyers, Ga., on May 20 was on Ritalin for depression.
Shawn Cooper, 15, who fired two shotgun rounds, narrowly missing students and teachers at his high school in Notus, Idaho, was also on Ritalin, for bipolar disorder.
Kip Kinkel, 15, was on Ritalin and Prozac. He murdered his parents and then went on to school where he fired on students in the cafeteria,…
Mitchell Johnson, the 13-year-old student at Westside Middle School in Jonesboro, Ark., who mowed down several children and a teacher with his friend Andrew Golden, 11, was on some sort of medication since he was being treated by a psychiatrist…..
http://www.ritalindeath.com/education/school-violence.htm

Then all you need to do is use the media to drive home the narrative ‘WHITE-SUPREMACISTS are TERRORISTS!

/FIN

Use USA LAW!

-GC

Newly Uncovered COVID Vaccine Contracts Lead Unexpectedly to Academic Corruption and Shill Science Attacks on Honest, Skeptical Scientists

A Gail Combs deep dive into a tangent of Karen Kingston’s latest revelation on Pfizer Comirnaty vaccine deaths and injuries, leads back to the war against truth-telling doctors and scientists – this time by their own CORRUPT university employers.

PREFACE by Wolf Moon

START HERE….

So who is BARDA?

And that brings me to the digging I have been doing.

August 2, 2021

Sidebar by Wolf – Dr. McCullough on Stew Peters

Dec 20 2021

June 8, 2021

NIH Clinical Trials Baylor: LINK

484 ACTIVE Studies found for: Baylor College of Medicine | Recruiting, Enrolling by invitation Studies

So is there a Robert Atmar – Hana El Sahly connection???

2022 Jan 26.

2022 Jan 26.

2021 Oct 15

EPub 2021 Sept 22Efficacy of the mRNA-1273 SARS-CoV-2 Vaccine at Completion of Blinded Phase.

PubMed lists: COVE Study Group [Corporate Author]

Wang EW, Parchem JG, Atmar RL, Clark EH.Open Forum Infect Dis.

-GC

Summary

W

How the Fake News, Social Media and the Deep State set up the Scamdemic behind our backs

Preface by Wolf Moon

CRITICAL TIMELINE

October 18 – 28, 2019

December 11, 2019 The Hill

December 31, 2019 The World Health Organization China Country Office is informed of a number cases of pneumonia of unknown etiology…

TEN NIH STUDIES ON ‘VACCINE REFUSAL’

Collaborators:

Facebook, Inc. aka Mark Zuckerberg who was Caught Stealing Election With Ballot Drop Boxes

-GC

Conclusion by Wolf Moon

W

A background research post by Gail Combs

PREFACE

by Wolf Moon

The Covid Second Opinion Forum

The Timeline of FDA Decisions

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

The VRBPAC Advisory Committee

To the Editors:

Vaccine Approval For Children

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.

Abstract

Current Projects

Papers:

2018

To the Editors:

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.

Summary

-Gail Combs

GC/wm (written/edited)

Introduction

HOARDING

THE GOVERNMENT AND ANTI-HOARDING

SUBCHAPTER I—PRIORITIES AND ALLOCATIONS Section 4512.

§4512. Hoarding of designated scarce materials

THE GRAIN CRISIS

a guest post by Gail Combs

(with a FREE SPEECH preface by Wolf Moon)

by Gail Combs

title and foreword by Wolf Moon

EPub 2021 Sept 22
Efficacy of the mRNA-1273 SARS-CoV-2 Vaccine at Completion of Blinded Phase.