Pfizer-BioNTech/COMIRNATY Vaccine Is Still Under “STUDY” Runs to be Completed at Different Intervals Between 2022-2026

” – known serious risks of myocarditis and pericarditis”

In addition to the many debates and conflicts surrounding the “approval” of the Pfizer/BioNTech/Comirnaty vaccine, there is interesting information to glean from the documents involved surrounding this controversy.

The below documents, some from the FDA’s own website, sheds further light into what seems to be a product still in its experimental/study phase. Some of the revelations are chilling, and doesn’t quite give the reassurance that an “approved” drug of this magnitude is more beneficial to us than what it is purported to be saving us from.

Screenshot of the FDA NEWS RELEASE: FDA Approves First COVID-19 Vaccine
taken on August 31, 2021
[ https://www.fda.gov/news-events/press-announcements/fda-approves-first-covid-19-vaccine ]
Content current as of August 23, 2021

Selected quotes in gray text boxes are from the above document:

“Specifically, in the FDA’s review for approval, the agency analyzed effectiveness data from approximately 20,000 vaccine and 20,000 placebo recipients ages 16 and older who did not have evidence of the COVID-19 virus infection within a week of receiving the second dose. The safety of Comirnaty was evaluated in approximately 22,000 people who received the vaccine and 22,000 people who received a placebo 16 years of age and older.

Based on results from the clinical trial, the vaccine was 91% effective in preventing COVID-19 disease.

More than half of the clinical trial participants were followed for safety outcomes for at least four months after the second dose. Overall, approximately 12,000 recipients have been followed for at least 6 months.

The most commonly reported side effects by those clinical trial participants who received Comirnaty were pain, redness and swelling at the injection site, fatigue, headache, muscle or joint pain, chills, and fever. The vaccine is effective in preventing COVID-19 and potentially serious outcomes including hospitalization and death.”

There are a couple of notes to take away from this document. In the above quote, it doesn’t quite specify how long the clinical trial lasted. Only that more than half of the clinical trial participants were followed for safety outcomes for 4 months after the second dose. It also states that 12,000 of the recipients were followed for at least 6 months.

Both of these numbers (4 and 6) are incredibly low quantities when taking into account pregnant women who are at the beginning of their pregnancy. The length of the clinical trial does not take into account the full 9 months needed to determine a healthy pregnancy, nor does it allow for any time to safely assess the development of the baby once born.

The data in this document also does not include differences between those of the placebo group compared to that of the “vaccine” group. In addition, if we are to only take the 12,000 participants into account, which from the wording of the document seems to allude that these are the recipients of the vaccine, that would still leave 10,000 participants unaccounted for. Just from the amount of vaccine recipients (22,000), this is 45% of their study that the data does not reflect. If we are to include the 22,000 of the participants who received the placebo, the data that was not tracked would rise to 72%.

There is also the challenge of how they determined that the vaccine actually prevented COVID. Were these recipients exposed to someone with COVID or were deliberately inoculated with the disease to see if they would get infected? Many people, myself included, have gone on for more than a year without developing COVID, or at least “COVID symptoms”. Since this data only involved a 4-6 month trial period, how many of us (vaccinated, placebo, or otherwise) can say that we have not contracted COVID during this time-frame either? Is this implying that unless you’re vaccinated, you will most likely get COVID every 4-6 months?

Another consideration to take into account are the many testimonies from well-respected and renowned doctors/scientists/virologists who are adamant in their assessment that these vaccines are unnecessary and instead further harms the immune system rather than help it.

In the same regard, those who are unvaccinated will obviously then not contract any of the possible side effects that are listed in this document as well as the many adverse events that are reported to VAERS. Which leaves one to wonder if the benefits really outweigh the risks of the COVID vaccines.

There is also the slight alteration on a different page of the FDA website that gives further clarification as to the efficacy of the COVID vaccines – which does not reflect that of what many people are influenced to believe:

Under the heading:

Q: What safety information did FDA evaluate to authorize the Pfizer-BioNTech COVID-19 Vaccine for emergency use and approve Comirnaty?

Screenshot of the Pfizer-BioNTech COVID-19 Vaccine Frequently Asked Questions
taken on August 31, 2021
[ https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/pfizer-biontech-covid-19-vaccine-frequently-asked-questions ]
Content Current as of August 23, 2021

UPDATE on September 6, 2021: Since the FDA website decided to remove this particular section from their FAQ (as of 9/1/2021), here is a screenshot taken from the web archive showing its existence:

“While the vaccine may not prevent infection, symptoms or transmission of the virus from person to person – “

This seems to be the heart of the matter, and although it continues with, “it is effective in preventing hospitalization and death.” it is in direct conflict with what we were led to believe this whole time. Most of the mainstream media, big tech platforms, health agencies, etc. have insisted that vaccines are needed to stop transmission of the virus and to protect those around us. However, this one simple statement defies everything that people were coerced into believing.

And with the last part of the sentence concluding that it prevents hospitalization and death, which even that is debatable when looking at the scope of the situation, it leaves one to wonder why this would not be an option for people to decide to take that risk on their own account. When comparing data of young individuals as well and their extremely low risk of hospitalization and death in the COVID setting, there ARE acknowledged threats when they are injected with the vaccine.

“Additionally, the FDA conducted a rigorous evaluation of the post-authorization safety surveillance data pertaining to myocarditis and pericarditis following administration of the Pfizer-BioNTech COVID-19 Vaccine and has determined that the data demonstrate increased risks, particularly within the seven days following the second dose. The observed risk is higher among males under 40 years of age compared to females and older males. The observed risk is highest in males 12 through 17 years of age. Available data from short-term follow-up suggest that most individuals have had resolution of symptoms. However, some individuals required intensive care support. Information is not yet available about potential long-term health outcomes. The Comirnaty Prescribing Information includes a warning about these risks.”

The FDA is also acknowledging that there are higher risks involved with the Pfizer-BioNTech COVID-19 vaccine and myocarditis and pericarditis, especially in males aged 12-17, and up to age 40.

“Information is not yet available about potential long-term health outcomes.”

“In addition, the FDA is requiring the company to conduct postmarketing studies to further assess the risks of myocarditis and pericarditis following vaccination with Comirnaty. These studies will include an evaluation of long-term outcomes among individuals who develop myocarditis following vaccination with Comirnaty. In addition, although not FDA requirements, the company has committed to additional post-marketing safety studies, including conducting a pregnancy registry study to evaluate pregnancy and infant outcomes after receipt of Comirnaty during pregnancy.”

The document is also stating that the possibility of myocarditis and pericarditis is an accepted issue and will continue to be monitored after the marketing of the Comirnaty vaccine.

And in a rather blunt admission, FDA states on their own website that Comirnaty is not required to evaluate pregnancy and infant outcomes after receipt of Comirnaty during pregnancy. This would explain why the initial trial run was only monitored for 4-6 months. An outline in the BLA (Biologics License Approval) also states that Comirnaty will conduct studies on this group as we see in a later section.

BLA documents state Comirnaty vaccine studies to be conducted for the next several years

Screenshot taken from from the FDA BLA Approval on August 31, 2021
[ https://www.fda.gov/media/151710/download ]
Document dated August 23, 2021

Text below is page 5 of the FDA BLA Approval document

Your deferred pediatric studies required under section 505B(a) of the Federal Food,
Drug, and Cosmetic Act (FDCA) are required postmarketing studies. The status of
these postmarketing studies must be reported according to 21 CFR 601.28 and section
505B(a)(4)(C) of the FDCA. In addition, section 506B of the FDCA and 21 CFR 601.70
require you to report annually on the status of any postmarketing commitments or
required studies or clinical trials.

Label your annual report as an “Annual Status Report of Postmarketing Study
Requirement/Commitments”
and submit it to the FDA each year within 60 calendar
days of the anniversary date of this letter until all Requirements and Commitments
subject to the reporting requirements under section 506B of the FDCA are released or
fulfilled. These required studies are listed below:

1. Deferred pediatric Study C4591001 to evaluate the safety and effectiveness of
COMIRNATY in children 12 years through 15 years of age.

Final Protocol Submission: October 7, 2020

Study Completion: May 31, 2023

Final Report Submission: October 31, 2023

2. Deferred pediatric Study C4591007 to evaluate the safety and effectiveness of
COMIRNATY in infants and children 6 months to <12 years of age.

Final Protocol Submission: February 8, 2021

Study Completion: November 30, 2023

Final Report Submission: May 31, 2024

3. Deferred pediatric Study C4591023 to evaluate the safety and effectiveness of
COMIRNATY in infants <6 months of age.

Final Protocol Submission: January 31, 2022

Study Completion: July 31, 2024

Final Report Submission: October 31, 2024

Submit the protocols to your IND 19736, with a cross-reference letter to this BLA STN
BL 125742 explaining that these protocols were submitted to the IND. Please refer to
the PMR sequential number for each study/clinical trial and the submission number as
shown in this letter.

Submit final study reports to this BLA STN BL 125742. In order for your PREA PMRs to
be considered fulfilled, you must submit and receive approval of an efficacy or a labeling supplement. For administrative purposes, all submissions related to these required
pediatric postmarketing studies must be clearly designated as:

• Required Pediatric Assessment(s)

As the document states, the completion study of Comirnaty postmarketing (after approval) is not due until May 31, 2023 / Novermber 20, 2023 / July 31, 2024 respective of older to lower age groups. There is also another important acronym to consider, which is the IND, which stands for Investigational New Drug.

With this knowledge in hand, it’s important to note that the clinical trial run was monitored for 4-6 months after the second dose on around 55% of the recipients, while the actual “approved” drug still in its investigational/study stages is set to be monitored for 2-3 years. This is a sizeable difference in the amount of time to determine safety and efficacy, especially when considering the many events already reported to VAERS. And according to the Pfizer-BioNTech COVID-19 Vaccine Frequently Asked Questions page from the FDA website:

Screenshot taken from the FDA Pfizer-BioNTech COVID-19 Vaccine Frequently Asked Questions
on August 31, 2021
[ https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/pfizer-biontech-covid-19-vaccine-frequently-asked-questions ]
Content current as of August 23, 2021

Q: Are vaccine providers required to report side effects?
A: Providers administering Comirnaty or Pfizer-BioNTech COVID-19 Vaccine must report to the Vaccine Adverse Event Reporting System (VAERS) and to Pfizer the following information associated with the vaccine of which they become aware:
  • Vaccine administration errors whether or not associated with an adverse event
  • Serious adverse events (irrespective of attribution to vaccination)
  • Cases of Multisystem Inflammatory Syndrome
  • Cases of COVID-19 that result in hospitalization or death

Acknowledged myocarditis and pericarditis issues being studied on children

” – known serious risks of myocarditis and pericarditis”

Screenshot taken from from the FDA BLA Approval on August 31, 2021
[ https://www.fda.gov/media/151710/download ]
Document dated August 23, 2021

Text in the gray box below are from pages 6-8 of the FDA BLA Approval documents
[ https://www.fda.gov/media/151710/download ]

We have determined that an analysis of spontaneous postmarketing adverse events
reported under section 505(k)(1) of the FDCA will not be sufficient to assess known
serious risks of myocarditis and pericarditis and identify an unexpected serious risk of
subclinical myocarditis.

Furthermore, the pharmacovigilance system that FDA is required to maintain under
section 505(k)(3) of the FDCA is not sufficient to assess these serious risks.

Therefore, based on appropriate scientific data, we have determined that you are
required to conduct the following studies:

4. Study C4591009, entitled “A Non-Interventional Post-Approval Safety Study of
the Pfizer-BioNTech COVID-19 mRNA Vaccine in the United States,” to evaluate
the occurrence of myocarditis and pericarditis following administration of
COMIRNATY.

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this study according to the following schedule:

Final Protocol Submission: August 31, 2021

Monitoring Report Submission: October 31, 2022

Interim Report Submission: October 31, 2023

Study Completion: June 30, 2025

Final Report Submission: October 31, 2025

5. Study C4591021, entitled “Post Conditional Approval Active Surveillance Study
Among Individuals in Europe Receiving the Pfizer-BioNTech Coronavirus Disease 2019 (COVID-19) Vaccine,” to evaluate the occurrence of myocarditis
and pericarditis following administration of COMIRNATY.

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this study according to the following schedule:

Final Protocol Submission: August 11, 2021

Progress Report Submission: September 30, 2021

Interim Report 1 Submission: March 31, 2022

Interim Report 2 Submission: September 30, 2022

Interim Report 3 Submission: March 31, 2023

Interim Report 4 Submission: September 30, 2023

Interim Report 5 Submission: March 31, 2024

Study Completion: March 31, 2024

Final Report Submission: September 30, 2024

6. Study C4591021 substudy to describe the natural history of myocarditis and
pericarditis following administration of COMIRNATY.

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this study according to the following schedule:

Final Protocol Submission: January 31, 2022

Study Completion: March 31, 2024

Final Report Submission: September 30, 2024

7. Study C4591036, a prospective cohort study with at least 5 years of follow-up for
potential long-term sequelae of myocarditis after vaccination (in collaboration
with Pediatric Heart Network).

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this study according to the following schedule:

Final Protocol Submission: November 30, 2021

Study Completion: December 31, 2026

Final Report Submission: May 31, 2027

8. Study C4591007 substudy to prospectively assess the incidence of subclinical
myocarditis following administration of the second dose of COMIRNATY in a
subset of participants 5 through 15 years of age.

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this assessment according to the following schedule:

Final Protocol Submission: September 30, 2021

Study Completion: November 30, 2023

Final Report Submission: May 31, 2024

9. Study C4591031 substudy to prospectively assess the incidence of subclinical
myocarditis following administration of a third dose of COMIRNATY in a subset of
participants 16 to 30 years of age.

We acknowledge the timetable you submitted on August 21, 2021, which states
that you will conduct this study according to the following schedule:

Final Protocol Submission: November 30, 2021

Study Completion: June 30, 2022

Final Report Submission: December 31, 2022

It is interesting that the timing to be considered for approval of these vaccines was only a 4-6 month timeframe, however, known dangers/risks, identified as “serious”, are still allowed to be approved and to be studied for 2+ years.

The document also recognizes that myocarditis and pericarditis is enough of a concern to happen after administration of the Comirnaty vaccine, since it mentions several studies just for this specific adverse event, and to continue to assess these reports.

In addition to all of the substudies to be conducted, there is a study to be initiated on a select group of participants to administer a third dose of the Comirnaty vaccine.

All of this information leads credence to the fact that even though the Comirnaty vaccine has “officially been approved” by the FDA, it is still in the investigational stages and being experimented upon on the public. And it goes without saying, but if myocarditis and pericarditis (on top of other reported side effects) are serious risks especially in children (“The observed risk is highest in males 12 through 17 years of age.”), then for this known risk to be offered to infants/toddlers defies any ethically moral boundaries and is in direct violations of the Nuremberg Code.

The next section also provides further evidence that there have been NO studies in the safety/efficacy of the Pfizer-BioNTech/Comirnaty vaccine on pregnant women.

Pregnancy/Births were not studied during the initial Pfizer-BioNTech/Comirnaty trial runs

Another snippet from the FDA Pfizer-BioNTech COVID-19 Vaccine Frequently Asked Questions website page, states the following:

Screenshot taken from the FDA Pfizer-BioNTech COVID-19 Vaccine Frequently Asked Questions
on August 31, 2021
[ https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/pfizer-biontech-covid-19-vaccine-frequently-asked-questions ]
Content current as of August 23, 2021

Q: Can pregnant or breastfeeding women receive the Comirnaty or Pfizer-BioNTech COVID-19 Vaccine?

A: While there have been no specific studies in these groups, there is no contraindication to receipt of the vaccine for pregnant or breastfeeding women. Pregnant or breastfeeding women should discuss potential benefits and risks of vaccination with their healthcare provider.

The acknowledgement above seems to indicate that the FDA and Pfizer-BioNTech/Comirnaty company have side-stepped this particular group in their vaccine studies, and have left it up to the healthcare provider to determine whether or not to administer this vaccine to pregnant women or women who are breastfeeding. This alone should be enough of a statement that there is no sufficient/professional data to analyze if the Comirnaty is safe during pregnancies/breastfeeding stages.

And if one were to consider the VAERS reporting system, in which the Pfizer-BioNTech company is required to report to, there have been numerous conditions of miscarriages/stillbirths/complications during pregnancy after administration of the COVID vaccine. While it is difficult to determine if these complications were a direct result of the vaccine, it is up to the scientific/healthcare community to investigate these cases in a thorough, unbiased and uninfluenced manner.

Another extremely alarming section of the FDA BLA Approval documents shows the following trial to be monitored in pregnant women:

Screenshot taken from from the FDA BLA Approval on August 31, 2021
[ https://www.fda.gov/media/151710/download ]
Document dated August 23, 2021

Text in the gray box below are from pages 9-10 of the FDA BLA Approval documents
[ https://www.fda.gov/media/151710/download ]
POSTMARKETING COMMITMENTS SUBJECT TO REPORTING REQUIREMENTS
UNDER SECTION 506B

We acknowledge your written commitments as described in your letter of August 21, 2021 as outlined below:

10. Study C4591022, entitled “Pfizer-BioNTech COVID-19 Vaccine Exposure during
Pregnancy: A Non-Interventional Post-Approval Safety Study of Pregnancy and
Infant Outcomes in the Organization of Teratology Information Specialists
(OTIS)/MotherToBaby Pregnancy Registry.”

Final Protocol Submission: July 1, 2021

Study Completion: June 30, 2025

Final Report Submission: December 31, 2025

There are a couple of key takeaways in this section that are of incredible importance. One major term to focus on is the word “NON-INTERVENTIONAL“.

According to What is a Non Interventional Study?, “In general, a non interventional study (NIS) (also called a non interventional trial) is where a patient takes regular medicine, prescribed according to the label. In an NIS, the researcher sets out to exert as little influence as possible on the patient’s condition while studying a medicine’s “…effectiveness, safety and tolerability under real life conditions” (Mishra & Vora, 2010).”

The article also reiterates multiple times that “non-interventional” studies are observational studies – the researchers are not to interfere with the dosages in any way but to prescribe them exactly as listed on the label. It also seems to imply that even if severe side effects show up, they are to still carry through with the “medicinal product” in that patient as prescribed. Another insinuation that one can make is that in order to not interfere with the study, it is not recommended to prescribe treatments that may help alleviate potential side effects. The term “tolerability” is implying to keep the patient going through the side effects in order to continue to study the long-term effects of the investigational new drug.

However, with the inclusion of “real life conditions”, it doesn’t indicate whether the patient can seek out physicians to investigate what is causing the side effects in their system and engage in therapeutic treatments to alleviate these effects. If a study is to be conducted in real life conditions, then it is to be expected that patients will seek treatments on their own while the researcher is only required to observe the patient to see how the alternative treatments interact with the drug/symptoms.

The same article goes on to state that the UK/EU have different definitions of what “non-interventional” means. “Aronson (2004) states… “the term ‘non-interventional’ in the Directive doesn’t mean non-interventional (i.e. non-interference) at all; it refers to an intervention with a licensed medicinal product.”

There is controversy and conflicts in this statement as another article, Interventional or Non-Interventional? Analyzing the Differences Between Clinical Studies Using Medicines in the European Union points out:

“Although defined in DIR 2001/20/EC, non-interventional studies are outside its scope. Due to the lack of harmonized regulation, some studies designed to be non‑interventional may be considered clinical trials by EU authorities. The two blinded studies described in Table 4 (see PDF) were considered clinical trials in the EU for planning on collection of data to support the marketing authorization application of experimental IMPs, despite no IMP being given and normal clinical practice being kept during the study period. Sponsors are thus advised to consult with authorities when planning studies under these conditions and/or whenever the objectives or design may raise questions.”

Further in the article, it states the following, which again, is not reassuring considering the policies/guidelines/mandates that authorities have been engaging in in order to mandate these investigational new drugs (COVID vaccines) onto the public:

“There is no centralized submission procedure for non-interventional studies with the exception of non-interventional PASSs, imposed as an obligation by an EU competent authority.{9} Because non-interventional studies do not have harmonized legislation, some Member States require submissions to regulatory authorities, while others do not. It is therefore important that sponsors are familiar with the regulatory framework of target EU Member States, and that they consult with local competent authorities and ethics committees (ECs) when justified.”

It’s sad to have to point this out, but the quote does specify “competent” authorities. And even the inclusion of “ethics committees” is not comforting seeing as how one of the leading figures in ethics study is Christine Grady, Chief of the Department of Bioethics at the National Institutes of Health Clinical Center, and wife of Anthony Fauci – Director of the National Institute of Allergy and Infectious Diseases and Chief Medical Advisor to the president, and who is also a large spokesperson for the experimental injections.

The other takeaway from section 10 of the FDA BLA documents is the term “TERATOLOGY“.

Definition of teratology
: the study of malformations or serious deviations from the normal type in developing organisms
merriam-webster/teratology

Teratology, branch of the biological sciences dealing with the causes, development, description, and classification of congenital malformations in plants and animals and with the experimental production, in some instances, of these malformations. Congenital malformations arise from interruption in the early development of the organism. Malformations in human infants, for example, may occur because the infant’s genotype contains mutant genes or includes an abnormal number of chromosomes; they also may occur if early in pregnancy the mother has had German measles (rubella), has taken some injurious drug, or has been exposed to an injurious dosage of radiation. Experimental studies suggest similar types of factors can cause malformations in animals and plants.”
britannica/teratology

Now when you combine the terms “non-interventional” and “teratology” together, it is suggesting that the ongoing studies (that were not conducted to begin with even in a clinical trial setting, as per the FDA’s own response) on pregnant women with Comirnaty and on the developing baby, will be monitored with as little intervention as possible and is mostly to be observed for malformations/genetic defects/miscarriages/etc.

In other words, safety and efficacy were never studied in this particular group, and neither was it studied in infants. It has also not been studied for long-term analysis, as the 4-6 month trial runs proves. The current “approval” it is undergoing now is an authorized experiment on the human population that is posing incredibly unnecessary risks when considering the many effective treatments that are already available to combat respiratory illnesses. And the insistent assertiveness to push this “investigational new drug” onto babies/children who are at extremely low risk for this illness is a disastrous decision from those in an “authoritative” position and should be investigated for malfeasance and misconduct.

This is also not the first time that government agencies/health industries/etc. have conducted experiments on the public.

The Tuskegee/Syphilis experiment was initiated onto a selection of African American men between 1932-1972. The study was only stopped (allegedly) after a publication was released on Associated Press in 1972 about the immorally unethical experiments being conducted on this group:

“Of about 600 Alabama black men who originally took part in the study, 200 or so were allowed to suffer the disease and its side effects without treatment, even after penicillin was discovered as a cure for syphilis. Treatment then probably could have saved or helped many of the experiment participants, PHS officials say.”AP WAS THERE: Black men untreated in Tuskegee Syphilis Study

This study seems to echo the sentiments we see going on with the coronavirus situation, in which only one type of drug is being promoted (the COVID vaccines) while suppression of other treatments that have been proven to work (such as Ivermectin) has been denounced by the very same government/health/medical fields that have conducted these experimental studies.

A study that involved the CDC/FDA’s approval, this time on Black and Latino babies, was conducted in the early 1990’s and involved the measles vaccine:

“1990: CDC Inoculated Black and Latino Babies with an Unlicensed Measles Vaccine
A covert clinical trial by the Center for Disease Control (CDC) and Kaiser Permanente inoculated Black and Latino babies with an experimental measles vaccine without informing parents the vaccine was experimental. More than 1500 six-month old black and Hispanic babies in Los Angeles are given the deadly “experimental” measles vaccine that had never been licensed for use in the United States; a vaccine that had been tested in African and Mexican babies resulting in high death rates. The parents were never informed and they never gave their consent. The CDC harmed babies, violated federal law, and trampled on parental rights with impunity.”
1990 FDA Issued a Waiver From Consent; Covert CDC Experimental Vaccine Test on Black / Latino Babies

It’s interesting that the measles vaccine experiment identifies Kaiser Permanente specifically, because as we see in another section of the FDA BLA Approval for Comirnaty, it seems as if Kaiser Permanente makes another appearance in the role of human experimentation:

Text in the gray box below is from page 10 of the FDA BLA Approval documents
[ https://www.fda.gov/media/151710/download ]

13. Study C4591014, entitled “Pfizer-BioNTech COVID-19 BNT162b2 Vaccine
Effectiveness Study – Kaiser Permanente Southern California.”

Final Protocol Submission: March 22, 2021

Study Completion: December 31, 2022

Final Report Submission: June 30, 2023

It would seem that the approval by the FDA of these IND drugs (Pfizer-BioNTech/Comirnaty vaccine) is a way for the government/health agencies to skirt away from liability by stating that since the vaccines are no longer “experimental” by their definition, and that they are FDA “approved”, it is no longer required to gain informed consent of these drugs. In addition, as to the technicality of their terms and protocols, there are a multitude of ways to interpret their “informed consent” rules, which officials can then bend or define in any way that best reflects the use of their study/drug.

[ https://www.fda.gov/regulatory-information/search-fda-guidance-documents/informed-consent#exceptions ]

Also keeping in mind how long it was determined before the “health agencies” granted approval of the Pfizer-BioNTech/Comirnaty vaccine – (4-6 months) – it would be conclusive to state that the vaccines have NOT sufficiently been studied in young children or pregnant women (or even the rest of the age groups because of the short amount of time the clinical trial study was conducted in), and the subsequent approval of this vaccine is to continue this research on the population who is exceedingly being pressured into taking this investigational new drug.

There is also the matter of the many adverse events that have been reported since the inoculation of these injections, that have largely gone unheeded within the health/medical institutions that are endorsing this drug. Other than the widely acknowledged myocarditis and pericarditis, most common in young males, which is still being studied and allowed to persist onto the public.

So again, taking into account the collusion of the government/health/medical/research fields to conduct experiments on the public, it would be necessary to reflect upon these agencies for additional breaches upon human rights, consent, and ethical behavior.

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Featured image by Ahmad Ardity from Pixabay

Anthony Fauci’s Wife: Christine Grady – Hidden Face of the Vaccine Trials?

What is Christine Grady’s role in the vaccine agenda?

One name that’s been front and center of the whole “coronavirus pandemic” is Anthony Fauci. I think we can all safely say that his is now a household name whose popularity exploded within the last year, year and a half.

Being appointed as the head of the coronavirus task force and the director of NIAID (U.S. National Institute of Allergy and Infectious Diseases) and a physician at NIH (National Institutes of Health), not to mention the chief medical advisor to numerous presidents throughout the years, it would seem as if our current situation rests squarely on his shoulders, as well as the collaborations he has with other organizations – CDC, FDA, WHO, UN, Silicon Valley, WEF, Wuhan lab, Bill and Melinda Gates Foundation, and so on.

However, one name who is also closely tied with Anthony Fauci and the unprecedented initiative to get the whole world vaccinated – is his wife, Christine Grady, whose name rarely comes up in the mainstream media.

Who is Christine Grady?

According to the following website:

Hm… already, I’m not liking the sounds of it.

“Human Subjects Research” … “bioethics” … “research subject recruitment, incentives, vulnerability”…

Kind of reminds me of what’s going on right now with the huge demand to vaccinate as many people as possible. We also have “incentives” to get the vaccine – travel, lotto, beer, donuts, concerts, cigarettes, etc., etc., etc. “Vulnerability”… well, there are task forces (Operation Homebound, for example) literally created for the sole purpose of aiming for the elderly and the mentally handicapped to get vaccinated, and now we are seeing huge efforts to get children vaccinated, even without the parent’s consent, and with the children being bribed with ice cream.

Very vulnerable groups, indeed.

Now one has to ask themselves, wouldn’t Christine Grady‘s position within the medical community as the Chief of the Department of Bioethics, as well as her role for obtaining human subjects for research, be in direct conflict with Anthony Fauci’s role as presidential and coronavirus advisor to administer a NEW vaccine that is only “authorized” – not approved – for emergency use only?

Keep in mind, the only reason why these vaccines are even authorized for emergency use to begin with is the belief that we are in an emergency situation, which, as anyone who has done proper research should know, the covid numbers have been drastically and fraudulently heightened to give the public the illusion that we are in a dangerous pandemic.

There are numerous reports coming out from esteemed doctors/physicians/scientists/lawyers, etc. who are willing to testify in court that the numbers of death from covid have been exaggerated, largely by abusing the PCR tests and labeling as many deaths as possible as covid – with the medical industry ALSO being incentivized with financial compensation to label them as covid – not to mention bribing families with free funeral services ONLY IF the death is labeled covid… (I think you can see where this is going) and that the vaccines themselves are an experimental trial initiated onto the public without their knowledge or consent.

Video: “Crimes Against Humanity”: The German Corona Investigation. “The PCR Pandemic”

Video: “All Roads Lead to the Vaccine”: Full Interview with Dr. Peter McCullough /
Renowned Texas Professor and Doctor: COVID-19 Shots Are “Bioweapons Thrust Upon the Public!”

Full video with Peter McCullough:

A short excerpt on Dr. Peter McCullough’s view on this strange situation with the vaccine propaganda:

Dr. Peter McCullough is one of the leading experts on COVID-19 treatments. He was the lead author of a study, published in the American Journal of Medicine last August, which has been cited over 600 times making him the most cited doctor by the National Library of Medicine regarding treatments.

McCullough has actually treated patients successful with medications that have long been approved to treat other viruses and diseases. The problem is, how can the government and corporations profit off drugs they don’t hold patents for? That’s why, according [to] McCullough, the propaganda of a vaccine being the savior has been pushed from the very start of the COVID-19 tyranny.

“So, the U.S. government has made a decision, along with the stakeholders – the CDC, NIH [National Institutes of Health], FDA, Big Pharma, World Health Organization, Gates Foundation – they have made a commitment to mass vaccination as the solution to the COVID pandemic and we are really going to be witness to what’s going to happen in history,” McCullough said in an interview. “We’re sitting on, right now, the biggest number of vaccine deaths, there’s been tens of thousands of hospitalizations, all attributable to the vaccine, and going strong.”

More and More Doctors Warning Against COVID Shots

Now, I want to bring your attention to the term “bioweapon” that Dr. McCullough mentions in his video. And the interesting correlation to the profession of “bioethic research” that Christine Grady is engaged in.

Merely a coincidence?

Combined with the DIRECT RELATION to Anthony Fauci, and his influence and “guidance” on the vaccination efforts, whose involvement with the Wuhan lab and now the controversy surrounding the gain-of-function research to deliberately create this virus – possibly as a means to justify enforcing the vaccine on the population – I’d say the conjecture of this being “just a coincidence” would only be to satiate those in extreme denial and refusal to admit that these corrupt medical industries have anything nefarious planned.

But with everything coming to light now, perhaps the public will finally realize what a sham the pharmaceutical company has been (or has become), and how there are organizations aiming for agendas that, while incredibly hard to believe, are unfortunately the only conclusion one can come to when honestly studying these groups and the plans that have been in the making for decades.

The REAL Purpose of the Covid Vaccine
The Corona Crisis: Has “Depopulation” Already Begun?

While everyone is focused on Gates and Fauci, and even Klaus Schwab for his “great reset” agenda, including the strangely similar “build back better” proposal, Christine Grady may, in fact, have more to do with these agendas than we’re led to believe. And perhaps is one of the key players in the driving force between dispensing these gene-therapy, mRNA vaccines onto the population.

Take into consideration the following ethically immoral case study of the Willowbrook experiment, that was conducted on innocent, mentally handicapped children from 1956 to the early 1970’s:

Nina became one of more than 50 mentally disabled children, ages 5 to 10, under the care of Dr. Saul Krugman, a respected pediatrician from New York who wanted to determine if there were multiple strains of hepatitis, and whether a vaccine could be created to protect against the disease. Krugman and his partner, Dr. Joan Giles, used the Willowbrook residents to test a preliminary vaccine for this disease that had killed millions worldwide. From 1955 to 1970, the children were injected with the virus itself or made to drink chocolate milk mixed with feces from other infected children in order to study their immunity.
The Hideous Truths of Testing Vaccines on Humans

There is NOTHING ethical about testing these types of experiments on human beings, much less those of defenseless children.

However, “Doctor” Krugman and others in his field may disagree, citing their own twisted point of view of what would designate, in their mind, an ethic experiment if it meant saving other people’s lives – even at the cost of inhumane subjugation of innocent, unknowing children – and adults, actually, as we can see from the Tuskegee Syphilis studies that were carried out under the deceptive pretense of helping black men survive a disease – even deliberately inoculating them with the disease, and then keeping the cure from them to watch the disease run its course.

Of course, that’s the official narrative. The speculated REAL purpose may have been even more sinister – a targeted experimental trial, with the added bonus of genociding a particular race.

Getting back to the horrendous Willowbrook experiment, we have our very own Christine Grady offering her two cents (again, who is the DIRECTOR of BIOETHICS and HUMAN SUBJECT RESEARCH):

To this day, while many modern-day ethicists use the Willowbrook studies as an example of unjust human experimentation, there are always second opinions. “It’s complicated,” Grady says. To her knowledge, “Krugman’s first goal was to understand the disease…but I think there are some things about it that certainly don’t look good and would be hard to get approval today.”
The Hideous Truths of Testing Vaccines on Humans

Notice that there is no condemnation on her part for the atrocious experiments conducted on innocent children. Only that “It’s complicated” and the hardships of getting such a trial approved.

No remorse. No condolences. No, “That was awful. As head of the bioethic human subjects research team, I am appalled at the level of inconsideration and cold, meticulous calculations of these scientists on human lives. The reason why I’m head of bioethics is to make sure this never happens again.”

… No… all we get is, (paraphrasing:) “It’s complicated. But we can’t blame Krugman because he was doing it to study the disease. Children? Who cares about the children? He was studying the disease. That’s far more important. And as for us in our current time frame, we’d have a much more difficult time getting approved for these types of study. Thankfully though, I’m the head of human subject research and so I’m able to approve things like this without too much difficulty.”

So we have to ask ourselves, are we willing to put the WHOLE WORLD in jeopardy when the director and head of bioethics and researching human subjects has the same mindset as Dr. Krugman, especially in regards to the rest of the children on the planet? The children who, “in our current time frame”, are being pressured and coerced, manipulated, “incentivized” into taking a gene altering, unapproved vaccine all for the sake of “research” or whatever else agenda is at play in the hands of corrupt billionaires?

Canadian Government Lures Children With Ice Cream To Take COVID Vaccine Without Parental Consent

Who REALLY benefits from these vaccines?

I have to reiterate again that these vaccines are unnecessary. Even if the coronavirus is a real ailment, the severity of it has been exaggerated and enhanced to present much higher cases and deaths than the true outcome. And the people affected are the elderly and those with pre-existing conditions – who are already vulnerable to these types of illnesses. Most of the population will be completely fine according to numerous honest physicians.

And I shouldn’t have to mention the efforts of the corrupt pharmaceutical companies and complicit big tech platforms/media to smear alternative medicine as a treatment to curing the coronavirus to begin with.

Hydroxychloroquine and Ivermectin has been highly targeted and censored, even banned in some countries, although they have continuously shown efficacy in treating covid and have been used throughout the medical community with large success. The HONEST doctors have also recommended plenty of sunshine and vitamin C/D to help combat these viruses.

So, to repeat the question, why are hydroxychloroquine/ivermectin, and the doctors who have documented successes with these alternative medicines, been ridiculed and smeared and attacked from certain propagators of the vaccine?

Hm… maybe because…IT ACTUALLY WORKS?

If these vaccines are for depopulation, like THOUSANDS of intelligent, professional, and rational individuals have surmised, then these alternative medicines are COUNTERING tptsb’s goal and, in their mind, must be stopped.

In the same vein, if these vaccines are (also?) for human research to see what these mRNA, CRISPR, gene-therapy, nanoparticles, hydrogel (or whatever they happen to be – perhaps all of the above) biotech does – then again, these alternative treatments must be stopped.

If the vaccines are to deliberately create illnesses, viruses, diseases in people for the sake of repeated customers for the pharmaceutical companies – who would profit IMMENSELY from people’s side effects – then these alternative treatments must be stopped.

And if the FDA is forced to recognize that these alternative medicines are actually working, then they cannot legally recommend these vaccines for emergency authorization use. Thus ending the huge worldwide vaccination effort.

Either way you look at it, the public doesn’t benefit from these vaccines. But the billionaire globalists and corrupt pharmaceutical companies do.

“Saving us from covid” was their planned strategy (Event 201) all along in order to get us all to take the vaccine.

Speculation and Theories

My guess, is that each vaccine from these big pharmaceutical companies, are particularly suited for a specific purpose. Perhaps Moderna addresses the mrna directly… can’t spell moderna without mrna, right? (Ode to mrna?) Again, this is just theories that may be way off base, but with the amount of information that is coming out that this has been a planned agenda and multiple companies/individuals are complicit, I wouldn’t put it past them.

Then there’s Pfizer/Biontech, which may be suited to more of the biotechnology such as the nanoparticles or lipid tech, etc. Again, these are just speculations. But with Mrs. Christine Grady-Fauci heading the teams on human subjects research, and her husband being the leading authority on vaccines and the coronavirus situation – as well as their close partnership with the Bill and Melinda Gates Foundation – I would say that these speculations probably aren’t too far-fetched of an idea. Especially now that people are realizing that Fauci had close ties with the Wuhan lab and funding of the gain-of-function research.

The Janssen (Johnson & Johnson) is another vaccine that offers a different method to tackle the human immune response system – I’m sorry, I mean, tackle the “coronavirus”, of course. We also have AstraZeneca and other variants of the vaccines as well.

Again, all of these vaccines are different in their structure not to address the best way to combat the coronavirus directly, like what the cover story is, but to simply see what these different technologies can do to the human system. After all, Christine Grady is head of human subjects research, and she saw nothing wrong with Dr. Krugman’s method of studying hepatitis who deliberately injected innocent children with the disease just to track its progress.

Now imagine the depopulation efforts, combined with new technology like CRISPR, mRNA, etc., as well as other people’s testimonies from decades ago warning the population that a dangerous bioweapon – like a vaccine – is in the works and is planned to be administered to the world population by any means necessary.

Here is a short snippet about vaccine developer Dr. Veert Ganden Bossche and his appeal to halt the vaccine trials:

In a recent turn of events Vaccine Developer Geert Vanden Bossche, Ph.D., DVM delivered a dire warning to mankind in an interview on March 8th, imploring all nations to immediately change course and halt the experimental COVID-19 vaccine trials. The future of the human race is at stake!

Dr. Bossche is a world leading vaccine scientist and virologist who worked for GAVI and the Bill and Melinda Gates Foundation. With credibility and expertise that’s off the charts and backed by sound science, Dr. Bossche instructed nations to HALT all COVID-19 vaccinations immediately, or an “uncontrollable monster” will be unleashed.

WORLD PUBLIC HEALTH EMERGENCY! Stop Big Pharma’s DNA “Vaccine” Experiment!

The link above shows Amazing Polly making this connection back in May of last year. All stemming from her investigation into one, seemingly innocuous tweet:

Realizing that “Christine Grady” was the only name not highlighted with a twitter account, Amazing Polly takes the initiative to research who she is and her relation to the covid-19 Ethical Challenges for Nurses agenda.

From there, the mind-boggling revelation that Christine Grady is MARRIED to our very own Anthony Fauci comes to light.

Amazing Polly also references a study that Christine Grady published under the name of “Four Paradigms of Clinical Research and Research Oversight”:

“She [Christine Grady] goes through medical research on human subjects, over the course of the last… 80 years or so, since WWII, and she categorizes the phases that they’ve gone through; and where she ends up, is that in 2005 we were getting into a communitarian based paradigm of human research subjects.

And what she essentially means is, they have made it so that the general public feels like it is their duty as humans to possibly sacrifice their own lives for medical research. They don’t even have to buy people anymore. Like, pay them. They don’t have to have people who are sick. They have now done such a mind job on the general public that they can convince a lot of perfectly healthy people to come in and let them experiment on them for free! For the “good of humanity”.

That’s where Christine Grady‘s head is at, in terms of her ethics.”

Amazing Polly

Keep in mind, that even if these people think that they are doing a public service to “save grandma” by injecting themselves with these suspicious/dangerous vaccines, the REAL underlying reason for these vaccines are anything BUT saving anyone. In fact, with more evidence coming to fruition about these corrupt agencies, it’s becoming clearer that the vaccines themselves are the TRUE disease, and that humankind would be best poised to avoid these at all costs for the good of humanity.

Speaking of “for the good of humanity”, where do we draw the line? If “studies” and “authority figures” come out saying that drinking the blood of the innocent is essential in saving humanity, would we all just jump in line and say, “Well, if it’s for the good of humanity, sign me up for a nice glass of young blood.”?

Silicon Valley’s fountain-of-youth plan to suck blood from young people just hit an FDA snag
Can Blood from Young People Slow Aging? Silicon Valley Has Bet Billions It Will

This sets an incredibly UNETHICAL precedent on what lengths people will go to to save their own life, or that of their loved one. Where do we draw the invisible/”let your conscience be your guide” line in terms of morally ethic or reprehensible actions on other people’s lives in order to save our own? When will we finally say that my life is not worth harming another, especially under the behest of inhumane scientific research and experimentation?

More importantly, how did studies/research like this even get the approval to begin with?

2. Radioactive Materials in Pregnant Women

2-Radioactive-Materials-in-Pregnant-Women

 

Image Source

 

“Shortly after World War II, with the impending Cold War forefront on the minds of Americans, many medical researchers were preoccupied with the idea of radioactivity and chemical warfare. In an experiment at Vanderbilt University, 829 pregnant women were given “vitamin drinks” they were told would improve the health of their unborn babies. Instead, the drinks contained radioactive iron and the researchers were studying how quickly the radioisotope crossed into the placenta. At least seven of the babies later died from cancers and leukemia, and the women themselves experienced rashes, bruises, anemia, loss of hair and tooth, and cancer.”

Source: The 30 Most Disturbing Human Experiments in History

“An exceptionally large-scale radiation exposure experiment at Vanderbilt University was funded by the U.S. Public Health Service and involved 820 poor pregnant Caucasian women who were given tracer doses of radioactive iron in a “cocktail” drink. The researchers worked with the Tennessee State Department of Health and they did not inform the women what was in the drink, nor were they informed that they were part of an experiment.”

1945–1947: Vanderbilt “Nutrition Study” Exposed 820 pregnant women to radioactive iron

One could argue that since most of these experiments happened in the mid-1900’s, that there’s no way that anything of the sort could be happening in today’s time. And perhaps that’s why a “bioethic” team was created to begin with. In order to halt experiments like this to begin with.

But I would disagree. The whole point of creating an organization focused on these kinds of questionable research and studies is to protect the agencies attempting these awful experiments and to create a shield, so to speak. It’s interesting that there’s a lot of inter-connected relations within these industries and partnerships that involve family members and friends working in conjunction with each other to support and/or condemn whoever they wish.

Another relation, Alison Fauci – daughter of Christine Grady and Anthony Fauci, works as a software engineer for Twitter. But I’m sure that has no connection to initiating “misinformation” tactics on the platform in order to protect this strange vaccination propaganda…

Twitter Suspends Organization for Announcing They Will Release More Fauci Emails | The Big Tech site cited their COVID-19 misinformation policy as a reason for the suspension

Even if Alison herself had no bearing on any so-called “misinformation” censoring/banning of accounts on Twitter, the point of having connected family members engaged in something as large as a worldwide medical enterprise to vaccinate every human being on the planet, and a huge platform such as Twitter banning any kind of information they deem as “harmful” or “inciting hate speech”/”misinformation”, cannot be overlooked.

Bottom line

It would seem from Christine Grady‘s job positions and titles, that her role is designated in how to best coerce, convince, bribe, reason, psychologically manipulate, etc. people into becoming willing participants in experiments and research – even if they don’t realize that’s what they’re signing up for. Would this role be helpful in getting as many people into taking these unnecessary vaccines – even possibly colluding with big tech platforms and mainstream media to deceive the public?…

I think the answer speaks for itself.

So are we sure we want to put our trust in the likes of Mrs. Grady (chief of the department of bioethics at the NIH/National Institutes of Health and director of Human Subjects Research) and her husband, Anthony Fauci (director of the NIAID/U.S. National Institute of Allergy and Infectious Diseases, physician with the NIH, and leading director of the White House coronavirus taskforce)?

And who could forget their close ties to Bill Gates… another huge controversial figure in regards to vaccines, eugenics, population control, and mad scientist efforts to block out the sun (interesting that there is a correlation between those actually with covid having a vitamin D deficiency…) and genetically mutated crops and mosquitos. Surely there’s no way he would endeavor to breach the morally bioethical line to genetically modify humans though, right?

…Nevermind.

Fact checking is extremely important. I want to reiterate not to take everything at face value; no matter what you read, where you read it from, or who you hear it from. And to be clear, do not rely on “fact checking” websites to give you accurate information either. These are just as likely, (if not even more likely…), to feed false information and false debunking accounts to manipulate the reader. Please take everything into consideration before adhering to a certain narrative – and always keep your mind open to other possibilities.

Fair use disclaimer: Some of the links from this article are provided from different sources/sites to give the reader extra information and cite the sources, but does not necessarily mean that I endorse the contents of the site itself. Additionally, I have tried to provide links to the contents that I used from other sites as an educational and/or entertainment means only; if you feel that any information deserves further citation or request to be clarified, please let me know through the contact page.

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FLASHBACK | COVER-UP: ‘Scientific Reductivism’, The Talented Mr. Fauci

A look into Anthony Fauci’s involvement into medical/health corruption.

In light of recent revelations, with the now admission from Fauci himself, that the coronavirus may have originated (been created) in the Wuhan lab instead of occurring naturally, and that it would be worth it to take a closer look –

(although last year every mainstream news media and “fact-checker” on the planet was insisting that this assertion was “debunked” and a “baseless conspiracy theory”)

– not to mention the gain of function controversy and the $600,000 funding (at least) that Fauci sent to the Wuhan Institute specifically for bat-to-human transmission viruses – and Fauci’s OWN admission in May 2020 that “The best evidence shows the virus behind the pandemic was not made in a lab in China”,

I felt it would be prudent to bring up the following article as a flashback to the corruption that Fauci and his cohorts have been engaged in with other viruses that have haunted humankind.

Before I get into that, I also want to highlight this particular section as another opportunity to present how many times the lead talking head of directing the coronavirus response has flip-flopped on his OPINION (NOT FACT) – on what should be founded on scientific basis and actual research, not just based on assumptions, “leanings”, and “indications”:

“If you look at the evolution of the virus in bats, and what’s out there now it’s very, very strongly leaning toward this [virus] could not have been artificially or deliberately manipulated—the way the mutations have naturally evolved,” he responded.

“A number of very qualified evolutionary biologists have said that everything about the stepwise evolution over time strongly indicates that it evolved in nature and then jumped species,” Fauci added.

In May 2021, PolitiFact’s Kate Sanders asked Fauci if he was “still confident” that COVID-19 developed in nature.

“No, actually … I am not convinced about that,” Dr. Fauci said. “I think we should continue to investigate what went on in China until we continue to find out to the best of our ability what happened.”

“Certainly, the people who investigated it say it likely was the emergence from an animal reservoir that then infected individuals,” he continued, “but it could have been something else, and we need to find that out. So, you know, that’s the reason why I said I’m perfectly in favor of any investigation that looks into the origin of the virus.”

– Source: Dr. Fauci Keeps Changing His Wuhan Lab Funding Story, Jay Battacharya Tells Laura Ingraham

Uh huh… And why has his sudden inclination to actually investigate the origins of the coronavirus instead of dismissing it as most likely from a natural biological transmission now such a huge agenda for Mr. Fauci? After A WHOLE YEAR of repeated insinuations that it was naturally occurring?

It couldn’t possibly have anything to do with Rand Paul’s testimony that he has proof that the gain-of-function research for this SPECIFIC virus came under the direction of Fauci and his institution, right? Exposing the relationship that Dr. Shi Zhengli (who perhaps unwittingly made mention of her collaboration) has with the NIH institution, thanking Fauci personally for funding the research at the end of her paper?

VIDEO: Rand Paul Says Fauci ‘Absolutely’ Committed Perjury When Denying Wuhan Gain-of-Function Research

Methinks the WHO is obviously complicit in this whole ordeal as well…

“A joint report into the origins of COVID by the World Health Organization (WHO) and China has found it is “extremely unlikely” that the virus escaped from a lab, according to a draft version seen by AP News.”
‘Extremely Unlikely’ COVID Came From Lab Draft WHO Report Says, As Ex-CDC Head Touts Claim

I don’t know if I have to mention it, but Mr. Fauci is not the only one who should be under the radar… We already know about Bill and Melinda Gates’ involvement in all of this as well, but what about Mrs. Fauci? What does she do, again?

“Christine Grady is an American nurse, bioethicist, and a senior investigator. She currently serves as the Chief of the Department of Bioethics at the National Institutes of Health Clinical Center. She also serves as Head of the Department’s Section on Human Subjects Research.”
Christine Grady Wiki Bio

“Head of the Department’s Section on Human Subjects Research

…Hmm… make of that what you will.

FLASHBACK: The original article was first published on April 05, 2020.

The following information has been reblogged from rielpolitick.com
(original post can be found at journal-neo.org | The Remarkable Doctor A. Fauci)

COVER-UP: ‘Scientific Reductivism’, The Talented Mr. Fauci

Source – journal-neo.org

“…Fauci, Birx and Redfield, all incestuously complicit in the HIV/AIDS frauds and malpractice, today hold the future of not only American public health, but also of the entire world economy in their hands. Not a good situation. As their work on the proved HIV=IDS fraud shows, the coronavirus tests do not at all prove presence of a deadly virus in any patient. If this is so, it is perhaps the greatest criminal fraud in medical history”

The Remarkable Doctor A. Fauci – By F. William Engdahl

Dramatic political and social decisions are being made across the United States and around the world on what emergency quarantine measures and other steps must be taken. In many cases the radical and severe measures, such as shutting down the world economy, are being justified by COVID-19 case projections of morbidity into the future. If there is one person who is the face of the current strategy of dealing with the coronavirus in Washington it is the Director of the US National Institute for Allergy and Infectious Diseases (NIAID) of the NIH, Dr. Tony Fauci. What major media conveniently leave out in discussing Fauci’s role is his highly controversial and conflicted history since he first joined NIAID in 1984 during the beginnings of the AIDS panic. His role then sheds valuable light on his remarkable and highly controversial actions today.

Tony Fauci, a leading member of the White House Coronavirus Task Force, is being promoted by major US media such as CNN, MSNBC or the New York Times as the great expert on all related to the Covid19 outbreak. He had dismissed the President’s efforts to promote a known malaria medication as treatment for severe corona patients as “anecdotal,” even though seven years before he backed the same drug. He has publicly taken projections from an institute created in Washington State by the Gates Foundation, the same foundation that virtually owns the WHO and owns major stakes in the leading vaccine makers, to claim that up to 200,000 Americans could die from COVID19. Fauci stated that COVID19 is “probably about 10 times more lethal than the seasonal flu,” which would mean 300-600,000 coronavirus deaths this year, at the same time in a respected medical journal he compared Covid-19 as similar to seasonal flu in morbidity. When questioned how long the shutdown of much of the US economy must last, Fauci replied only when there is zero new covid19 positive tested cases, something impossible given the defective testing. He has also backed direct human tests of novel vaccines with no prior animal tests, including with radical non-tested mRNA gene-edited vaccines.

Fauci has more influence over US national policy on the unprecedented Covid-19 pandemic than anyone, including the President.

Much of media treats him with awe as an unimpeachable scientist, one of the world’s finest. A closer look at Anthony Fauci’s career gives a starkly different picture, a very alarming one in fact.

America’s AIDS Czar

Tony Fauci has held the top post at the NIAID in Washington for an astonishing 36 years. Today he is well past retirement age at 79, and holds the funds to determine which drug companies or university researchers will get precious government funds or not from NIAID’s annual $5 billion budget.

Let’s go back to 1984 when Fauci was named head of NIAID during the Reagan era. That year an AIDS researcher, Robert Gallo, working under Fauci, held a press conference to announce that he had “discovered” the AIDS virus. He said it was HIV– human immunodeficiency virus. The shocking announcement which went around the world, was in complete disregard of scientific procedures of prior peer-reviewed published scientific evidence, including the required electron microscope analyses. It was a case of “science by press conference” as a critical scientist, Prof. Peter H. Duesberg described it. Duesberg was an award-winning researcher at Berkeley who isolated the first cancer gene through his work on retroviruses in 1970, and mapped the genetic structure of these viruses.

For Gallo and Fauci, that was unimportant as millions in research funds flowed into NIAID to research the new virus, HIV. Fauci and Gallo claimed that AIDS was highly contagious, also by sexual transmission, especially among homosexual men. Notably, before the Gallo claim to have found the HIV AIDS virus, NIAID had been doing research on the role of drugs, poppers or nitrites, proven immune-suppressants, in the deaths of the earliest AIDS patients. That was quickly dropped in favor of researching a “cure” for AIDS. Media was told that AIDS was the “public health threat of the Century.” Gallo went on to make millions on his patented blood test for HIV, despite the fact that the test was often giving false positives and did not test directly for the alleged virus but for active antibodies, something immunology practice said was not valid, as antibodies merely suggested a past infection response and not necessarily presence of AHIV. At this time in the 1980’S Fauci was responsible for AIDS research at NIAID, a post he still holds.

False Tests?

The issue of HIV/AIDS tests is central. While a frightened world was clamoring for a test, Gallo and Fauci promoted their deeply flawed tests of antibodies. In 2006 Gallo claimed, “HIV tests were highly accurate from the time they were developed in 1984 and have become much more accurate over time…” Highly accurate in 1984 but more accurate than highly over time? Gallo added in response to criticism, “A PCR test for the presence of the virus itself can accurately determine a child’s HIV status.”

In a sharp rebuttal of the Gallo claims, claims endorsed by Fauci and the NIAID as well as CDC, Roberto A. Giraldo, MD and Etienne de Harven, MD, the scientist who produced the first electron micrograph of a retrovirus, pointed out that both the ELISA and Western blot, and a genetic test, the PCR or ‘Viral Load’ test,” the two major tests used to determine if one has AIDS, are invalid. “None of these tests detect the HIV virus itself, nor do they detect HIV particles.” They add that there are “more than 70 different documented conditions that can cause the antibody tests to react positive without an HIV infection.” Among the false positive cases are influenza, the common cold, leprosy or the existence of pregnancy. The same tests are used today to determine SARS-CoV-2-positive.

They concluded, “The fact that after 25 years of intense research HIV has been neither isolated nor purified in terms of classical virology indicates to us that the infectious view of AIDS as a contagious viral disease is based on an apparently non-existent microbe!”

Giraldo and de Harven declared, “The alleged existence of HIV was asserted from the study of proteins, reverse transcriptase activity (RT), and RNA fragments that were found in culture supernatants, not from the direct analysis of purified viral particles.” The CDC requires a positive antibody test for HIV to determine AIDS in the USA. Yet in Africa since 1985 the WHO requires no HIV test or any other laboratory test. Merely the patient’s symptoms that can include weight loss, chronic diarrhea, prolonged fever, persistent cough and such, symptoms endemic to chronic poverty, malnutrition and lack of sanitation.

Yet this fraud has shaped the career of Tony Fauci for more than 35 years. Fauci as head of NIAID has taken millions from the Bill & Melinda Gates Foundation as well as the Clinton Foundation along with tens of billions from US taxpayers for this bogus research. Suspiciously, the 2006 article by Giraldo and de Harven was suddenly retracted by the journal in 2019 just before the coronavirus Wuhan outbreak.

Despite the fact that he knew the established rules of virology, Fauci, as head of NIAID, recommended the Burroughs Wellcome chemotherapy drug, AZT as a “preventive drug” for HIV diagnosed patients even without symptoms! Burroughs Wellcome gave NIAID the study that was deliberately biased for AZT. Fauci even backed AZT for pregnant women despite the grave risk to the fetus.

One mark of pregnancy in all women is a higher level of antigens as the natural immune system fights any infection to protect the fetus. AZT or Retrovir, a failed leukemia drug, has been proven to be a highly toxic drug. It was approved for AIDS testing in a record 5 days by Fauci and the US Government in 1987. Today despite more than thirty years funded research and billions of dollars, no effective vaccine for HIV/AIDS exists.

Fauci and Gilead

According to people who have studied the role of Tony Fauci as head of NIAID, his focus has been what is called scientific reductivism, described as “a 19 Century-style, single-germ theory for a complex web of factors that collapsed the immune systems of a subset of gay men in the early 1980s.” He has refused to explore the documentation that a variety of lethal drugs and other toxins such as nitrites could play a role. As a result he has wasted tens of billions of taxpayer dollars since 1984 on dead end experiments.

One of his most nefarious was his collaboration with Gilead Sciences.

Not satisfied with having developed a false positive test for AIDS and having gained FDA fast-track approval for AZT to treat HIV-positive patients with serious illness symptoms, Fauci decided to collaborate with Gilead (as in the Biblical “balm of Gilead”) on what came to be called PrEP experiments.

Fauci in 2007 began to finance clinical trials of the AZT drugs in HIV “negatives,” on the theory the chemotherapy would “protect” them from becoming “positive.” That is, testing toxic HIV drugs on otherwise healthy persons to “insure” they never got AIDS. If it sounds mad, it was. Gilead supplied the drug, Truvada, to NIAID between 2007-2012 for Phase III human tests on HIV negative subjects. Four tests of at least 2,000 and up to 5,000 test subjects each, were done. The project was called “pre-exposure prophylaxis” or “PrEP.” Healthy subjects were given doses of chemotherapy drug Truvada on the thesis it could prevent them from one day getting HIV-positive. CDC, in its May 2014 recommendation urged physicians to prescribe Truvada for negatives in the so-called “risk groups,” an official government imprimatur for an extremely profitable drug.

The FDA ignored two of the four Truvada tests that had failed and been halted. Despite that and owing to data manipulation by Fauci’s NIAID and Gilead, the FDA approved the dangerous Truvada for PrEP. Today Gilead lists the side effects of Truvada: Kidney problems, including kidney failure; worsening Hepatitis B; too much lactic acid in your blood (lactic acidosis), which can lead to death; severe liver problems, which can lead to death; bone problems. They state that Truvada “can help reduce the risk of getting HIV-1 through sex, when taken every day and used together with safer sex practices.”

The Fauci-Gilead scam of promoting Truvada for healthy people to “reduce risk” of HIV is a marker for the level of medical malpractice and in some cases evident criminal abuse of human health that the current White House coronavirus guru, A. Fauci, represents.

Fauci and COVID-19

In October, 2019 Fauci and his NIAID got $100 million from the Gates Foundation to develop “gene-based” therapies for HIV and sickle cell disease. That means Fauci still to the time of the first claims of novel coronavirus in Wuhan China, Fauci was still promoting a 35-year fraud around HIV. Fauci is also part of the Gates Foundation cabal. In 2012 Fauci was named one of the five Leadership Council of the Gates Foundation-created Global Vaccine Action Plan.

This is highly relevant to his role today as the Trump Administration coronavirus “pope.” Has his NIAID or any other laboratory in the world rigorously, with electron microscopy, isolated and purified samples of patients tested SARS-CoV-2 positive for Covid-19? Or are the virus proofs as faulty as Fauci and the AIDS clique have made for HIV?

In addition NIAID is working with Gilead to conduct Phase II human trials on Gilead’s drug, remdesivir, as a potential treatment for hospitalized adult patients diagnosed with COVID-19.

A coincidence?

Relevant also is the fact that all top scientific advisers to the US President’s Task Force on COVID-19 are tied since decades to the bogus and destructive HIV/AIDS research and propagation of false theories. Alongside Tony Fauci of NIAID stands Deborah L. Birx, M.D., Obama appointee as US Global AIDS Coordinator who worked under Tony Fauci at NIAID from 1983-1986.

Robert Redfield is the current Director of the Centers for Disease Control and Prevention, center of the recent coronavirus testing scandal. Redfield cofounded with the discredited Robert Gallo, former Fauci colleague in the AIDS scandals of the early 1980’s at NIH, the Institute of Human Virology based at University of Maryland. Redfield and Birx also coauthored numerous scientific articles on purported HIV vaccines, none of which have been effective.

Fauci, Birx and Redfield, all incestuously complicit in the HIV/AIDS frauds and malpractice, today hold the future of not only American public health, but also of the entire world economy in their hands. Not a good situation. As their work on the proved HIV=IDS fraud shows, the coronavirus tests do not at all prove presence of a deadly virus in any patient. If this is so, it is perhaps the greatest criminal fraud in medical history.

_____________________

F. William Engdahl is strategic risk consultant and lecturer, he holds a degree in politics from Princeton University and is a best-selling author on oil and geopolitics, exclusively for the online magazine “New Eastern Outlook.”

https://journal-neo.org/2020/04/15/the-remarkable-doctor-a-fauci/

ONE LAST NOTE FROM E.A.R. (excerpt below taken from the post “Anthony Fauci Caught ‘Lying’ – Several Times”)

An interesting piece from 1994 on Kary Mullis and his views on a couple of questionable individuals:

In the end, “Nightline” ran a two-part series, the first on Kary Mullis, the second on the HIV debate. Mullis was hired by ABC for a two-week period, to act as their scientific consultant and direct them to sources.

The show was superb, and represented a historic turning point, possibly even the end of the seven-year media blackout on the HIV debate. But it still didn’t fulfill Mullis’ ultimate fantasy. “What ABC needs to do,” says Mullis, “is talk to [Chairman of the National Institutes of Allergy and Infectious Diseases (NIAID) Dr. Anthony] Fauci and [Dr. Robert] Gallo [one of the discoverers of HIV] and show that they’re assholes, which I could do in ten minutes.

But I point out, Gallo will refuse to discuss the HIV debate, just as he’s always done.

“I know he will,” Mullis shoots back, anger rising in his voice. “But you know what? I would be willing to chase the little bastard from his car to his office and say, ‘This is Kary Mullis trying to ask you a goddamn simple question,’ and let the cameras follow. If people think I’m a crazy person, that’s okay. But here’s a Nobel Prize-winner trying to ask a simple question from those who spent $22 billion and killed 100,000 people. It has to be on TV. It’s a visual thing. I’m not unwilling to do something like that.”

He pauses, then continues. “And I don’t care about making an ass of myself because most people realize I am one.”

(Kary Mullis)
The Corona Simulation Machine: Why the Inventor of The “Corona Test” Would Have Warned Us Not To Use It To Detect A Virus

It seems as if this self-described “ass” actually has a heart of gold and was trying to expose possible corruption as early as the 1990’s.

As Celia Farber, the interviewer, mentions: “One time, in 1994, when I called to talk to him about how PCR was being weaponized to “prove,” almost a decade after it was asserted, that HIV caused AIDS, he actually came to tears.

Sadly Kary Mullis passed away on August 17, 2019, allegedly from pneumonia. Just weeks away from when Event 201 took place in October 2019, and a few more weeks from when an actual “surprise outbreak” erupted, allegedly as early as November 2019. And just a couple of months after that, we have the PCR tests that Mr. Kary Mullis himself invented and was against using for viral detection, being used (and abused) for viral detection en masse – at the behest of the “expert scientists”.

Fact checking is extremely important. I want to reiterate not to take everything at face value; no matter what you read, where you read it from, or who you hear it from. And to be clear, do not rely on “fact checking” websites to give you accurate information either. These are just as likely, (if not even more likely…), to feed false information and false debunking accounts to manipulate the reader. Please take everything into consideration before adhering to a certain narrative – and always keep your mind open to other possibilities.

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