Nobody Is Safe Until Everybody Is Safe

judiciary.house.gov  |  Today, the House Judiciary Subcommittee on the Administrative State, Regulatory Reform, and Antitrust, led by Chairman Thomas Massie (R-KY), released an interim staff report titled, "Politics, Private Interests, and the Biden Administration's Deviation from Agency Regulations in the COVID-19 Pandemic" The report details how the Biden Administration pressured the Food and Drug Administration (FDA) to go beyond its regulatory authority to change its procedures, cut corners, and lower agency standards to approve the Pfizer COVID-19 vaccine and authorize boosters. This approval enabled the Biden Administration to mandate the COVID-19 vaccine, despite concerns that the same vaccine was causing injury among otherwise healthy young Americans. 

"In August 2021, when the Pfizer shots received FDA licensure, and just before the booster received EUA, the top two FDA vaccine reviewers with decades of experience announced they were leaving the agency," said Chairman Thomas Massie (R-KY). "During the pandemic, politics overruled science at the government institutions entrusted with protecting public health. The FDA abandoned its congressional directive to protect citizens from false claims and undisclosed side effects, and instead ignored its own rules to pursue a policy of promoting the vaccine while downplaying potential harms. Exposing and acknowledging mistakes that were made is a necessary step toward restoring integrity and trust in our regulatory agencies."

The Subcommittee's investigation also revealed that the administrative state mishandled reports of vaccine injury, despite requirements to actively obtain, synthesize, and report feedback on the safety and efficacy of the Emergency Use Authorization (EUA) vaccine. Two former FDA scientists, Dr. Marion Gruber and Dr. Philip Krause, testified to the Subcommittee that they felt pressure to cut corners on the vaccine review, which was due to outside pressure to provide immediate approval so that the government could mandate vaccines. Despite evidence of harms from the EUA vaccine, the Biden Administration sought to fully approve the Pfizer vaccine through the Biologics Licensing Application (BLA) process.

Under the leadership of then-Acting FDA Commissioner Dr. Janet Woodcock, a long-time FDA staffer who the Biden Administration promoted to Acting Commissioner, and Dr. Peter Marks, head of the FDA's Center for Biologics Evaluation and Research (CBER), the agency cut corners in its usually rigorous BLA process to brand the Pfizer EUA vaccine as the only fully licensed "safe and effective" COVID-19 vaccine on the market at the time.  Today, former Acting FDA Commissioner Woodcock says that, as it relates to vaccine-related injury, she is "disappointed in [her]self" and that the FDA did not do enough to address vaccine-related injury.

The FDA succumbed to the Biden Administration's pressure to act beyond its authority, which may have long-term impacts on the agency's ability to confidently serve the American public. This poor policy by the Biden Administration reveals many significant problems related to accountability and good decision making in the administrative state that warrant legislative reform. 

Read the full interim staff report and appendix here.

The Wuhan Cover-Up by RFK Jr.

brownstone  |  In the final chapters of The Wuhan Cover-Up, RFK, Jr. focuses on several key figures in the biowarfare-industrial-complex, including Jeremy Farrar of the Wellcome Trust (now at the WHO), Anthony Fauci of the NIH, and Bill Gates. 

RFK, Jr. uses these figures to show how the Covid pandemic emerged from the toxic stew of ethically compromised biowarfare research standards; military, intelligence, public health, and academic institutions/organizations dependent on biowarfare funding; the involvement of China and global interests in the booming business of “pandemic preparedness and response;” and, of course, the endless pursuit of political power and personal enrichment.

Here’s a great summary of how they all came together, through personal and institutional greed and power-mongering, to unleash the Covid catastrophe on the world:

The evidence suggests that instead of relentlessly protecting public health, Farrar exploited the pandemic to promote the venal financial agendas of his WEF [World Economic Forum] patrons, to transform Western democracies into surveillance states, to expand his personal power and paycheck, and to pander to high-level Chinese officials. Achieving these objectives required Farrar to hide [Covid’s] laboratory origins, a project in which he enlisted a cadre of his medical cartel cronies—those who, thanks to years of funding by Fauci, Farrar, and Gates, now occupy the highest echelons of virology in academia, the regulatory agencies, and pharmaceutical companies. 

(p. 539)

If for nothing else, I would recommend adding The Wuhan Cover-Up to your library as an invaluable resource on leading figures, organizations, and power brokers involved in the biowarfare-industrial-complex.

Conclusions and Comments

It was especially gratifying to me to read The Wuhan Cover-Up (all 600 pages of it), because it validated my own research, showing that the pandemic response was led by the national security/intelligence arms of government, not public health agencies. 

In fact, after reading the first few chapters – the ones that go into the history of chemical and biological warfare and the rise of the biowarfare-industrial-complex – I paradoxically felt an enormous sense of relief. 

Finally, we have a detailed account that shows – beyond what I would consider a reasonable doubt – that the entire Covid catastrophe was caused, and led, by a multinational military-intelligence-academic-pharma-tech-NGO cabal.

RFK, Jr.’s conclusion is that we should look to a future “in which the bio-elites are held responsible for their actions, people regain their rights, and the Constitution is restored to its intended preeminence.”

But how do we do that? 

I am afraid, based on the information in his own book, and the fact that RFK, Jr. himself is being censored and banned so extensively from the public square, that the solution to the problems he exposes is much more difficult and complex than just “holding the bio-elites responsible” which will somehow lead to people regaining their rights.

What we need to do is to shut down, or extract ourselves from, the global biowarfare-industrial-complex that is able to convince (or coerce?) our governments into declaring states of emergency over supposed pandemic threats, and then curtail civil rights and impose massive surveillance, censorship, and propaganda that would not be permitted in non-emergency situations. Not to mention garnering enormous wealth while forcing the world’s population to accept novel, untested, and potentially lethal medical “countermeasures.”

The Wuhan Cover-Up does a better job than any other book or article I have read at exposing the trends, forces, and institutions that brought us the Covid catastrophe – with hundreds of pages of notes and references. What’s frightening is that the enormity of the problem is beyond the scope of the book, not just to solve, but even to fully acknowledge.

They Must Really Think You're Stupid!!!

attorneycox  |  The “they” is our government (federal and state). The “we” is you and me, and the other 300+ million Americans across our country.

Alas, here we are, entering the final quarter of 2023, and we have the United States government, and many state governments (including New York’s former Governor Andrew Cuomo, current left-wing Governor Kathy Hochul, and the super-majority Dem legislature) proclaiming for all to hear that they did not force anyone to do anything detrimental these past 3.5 years. UNBELIEVABLE! Did you hear this? They are actually saying with straight faces that they didn’t force you to wear a mask, or lockdown and shutter your businesses, or choose between taking an experimental drug or losing your job… Nope! They did none of that. And you - well, you are flat out crazy if you think they did. You are lying. You are exaggerating and totally overreacting.

Unfortunately for Big Brother, ooops, I mean unfortunately for our 100% reliable, never-lies-to-us government, we have actual documents (including lawsuits), news stories, social media posts, and videos of the government at all levels mandating and forcing us to do all of those things, and more. Here’s just one example of Biden himself, the “Big Guy,” mandating the C19 shot:

Biden is not alone. No, no. His entire administration is right there with him. His head of OSHA, Douglas Parker, is also now lying through his teeth about the OSHA mandate that REQUIRED (not suggested) that all employers in the entire nation with 100 or more employees force their employees to get the C19 shot, otherwise they had to wear a mask and test constantly for C19. (That OSHA mandate was struck down by SCOTUS last year because it was unconstitutional, by the way). Then there’s the head of HHS, Xavier Becerra, saying there was never a mask mandate. What?! Another blatant lie.

Please take the 2 minutes to watch this Congressman Kevin Kiley clip. You truly won’t believe your ears with the bullsh#* these Biden agency heads are spewing! As Congressman Kiley says in the video, the government is trying to tell us that “2 + 2 doesn’t equal 4.” You don’t get much more Orwellian than that!

CLICK HERE TO LISTEN

Why are they backtracking now?

Easy answers: 1) they didn’t have the authority to do any of it (all of it was unconstitutional) so they can’t justify and defend it now, and 2) if they can convince you they didn’t do it before, then you won’t mind as much when they do it again.

This should make your blood boil. It’s particularly infuriating to those of us who were speaking out from basically day one trying to tell people that the lockdowns, the masking, the shots, the limited number of people at your wedding or at your Thanksgiving table were all violations of the Constitution and our basic human rights!

Marshall Mcluhan: One Of The Big Marks Of The Loss Of Identity Is Nostalgia

mcluhangalaxy  |  “We have never stopped interfering drastically with ourselves by every technology we could latch onto,” Marshall McLuhan said in 1966. “We have absolutely disrupted our lives over and over again. Unimpeded, the logic of this sort of world is stasis.”

McLuhan believed deeply in man’s need to comfort his self from the onslaught of a world that seemed hostile from birth, and while masturbation is the act of physically imitating creation, it is in creating false media environments that man has found the greatest comfort for his psyche.

Were McLuhan alive today, he would perhaps take great interest in two particular aspects of modern society. The first of these aspects is the increasingly violent nature of our world, in both the physical world and its various media counterparts.

“When you live out on the frontier, you have no identity, you are a nobody, therefore you get very tough,” he said in 1977. “You have to prove you are somebody, and so you become very violent…ordinary people find the need for violence as they lose their identities.”

What does this say about a world where violence, both real and imagined, increases at a rate matched only by the proliferation of new media? I believe it says that media is responsible for a world that is increasingly violent, but not in a manner that censoring sex and violence is capable of curbing. The nature of media is that which it is given by man, and we have given it the nature of removing from us our natural selves. We relinquish aspects of our identity so that we might take shelter in the constructs that we have created to shield us from the harsh frontiers we encounter. At each new threshold, collective identity is lost, and with each new loss comes an increase in our capacity for violence.

If Marshal McLuhan had lived to see his 100th year in 2011, he might have marveled less at our technology than at our hunger for nostalgia. It was an area of particular interest for the author and media scholar, who said that one result of the electronic age would be a loss of private identity owing to the discarnate being that one becomes when broadcast electronically. Lacking a physical body in the electronic sphere, one’s relationship to the world around them changes.

“One of the big marks of the loss of identity is nostalgia, revivals of clothing, dances, music and shows,” he said. “We live by the revival, it tells us who we are, or were.”

Thus I commemorate Marshall McLuhan’s discarnate being, which lives on through his own self-interferences, with the most sincere sense of nostalgia of which one is capable. ■ http://www.psuvanguard.com/arts-culture/the-message-1.2469137

The Solution To Black On Black Gun Violence (REDUX Originally Posted 2/12/15)

AmericanThinker |  Sociology, which is sometimes defined as the painful and tedious explication of the obvious, occasionally comes up with useful insights, or at least proof that some useful insights are true. That seems to be the case with a study by Yale sociologist Andrew Papachristos, published in the academic journal Social Science & Medicine, and featured in the Chicago Sun-Times.

It turns out that being arrested with someone else is the best predictor of who will get shot in Chicago. No, not by the police, as the Al Sharptons of the world would like to claim. Shot by another civilian, in the epidemic of shootings that have made Chicago at some times more dangerous than Baghdad.

If you and another person get arrested together in Chicago, you’re both part of a loose network of people with a high risk of getting shot in the future, Yale University researchers say in a newly published study.
Only 6 percent of the people in Chicago between 2006 and 2012 were listed on arrest reports as co-offenders in crimes, the study says. But those people became the victims of 70 percent of the nonfatal shootings in the city over the same period.

The logic is pretty simple: if you are the type of person who goes out and commits crimes with others, you are probably connected to people who commit crimes with some frequency.  And that puts you at risk of getting shot, because people who commit crimes sometimes shoot others who become inconvenient, or who just get in the way.

The study is done with social network analysis, studying who knows who and how they interact, and drawing up networks that reveal the clustering that results from various commonalities.

 The latest Yale University study was built on Papachristos’ previous social-network research into murders on the West Side. He had studied killings between 2005 and 2010 in West Garfield Park and North Lawndale. About 70 percent of the killings occurred in what Papachristos found was a social network of only about 1,600 people — out of a population of about 80,000 in those neighborhoods. Inside that social network, the risk of being killed was 30 out of 1,000. For the others in those neighborhoods, the risk of getting murdered was less than one in 1,000.

These statistics demonstrate the wisdom of the old adage, “Lie down with dogs, wake up with fleas.” They also show that it is not per se that is related to the higher incidence of violence in some black communities…

For every 100,000 people, an average of one white person, 28 Hispanics and 113 blacks became victims of nonfatal shootings every year in Chicago over the six-year study period.

… but rather the existence of networks of people who engage in violence and reinforce each other in patters of violent behavior.

There are some useful implications for policing in Chicago IF the race demagogues don’t start calling it profiling: Fist tap Big Don.

UMKC |  An ongoing law enforcement effort to rethink strategies to reduce violent crime in the Kansas City area has its own secret weapon: UMKC.

The University of Missouri-Kansas City’s Department of Criminal Justice and Criminology, part of the university’s College of Arts and Sciences, is intimately involved in the Kansas City No Violence Alliance (NoVA). NoVA is a 2-year-old multi-agency effort to reduce gun-related violence.

Chancellor Leo E. Morton serves on NoVA’s governing board, and UMKC faculty members and graduate students are embedded in NoVA’s effort to implement a crime-prevention approach known as “focused deterrence,” which helps police look beyond individual criminals to the criminals’ entire social networks.

The International Association of Chiefs of Police this month called out UMKC’s relationship with the Kansas City, Missouri, Police Department through NoVA when it awarded the department its 2014 bronze medal for Excellence in Law Enforcement Research Award. The award recognizes law enforcement agencies that demonstrate excellence in conducting and using research to improve police operations and public safety.

UMKC became involved with NoVA at the very beginning. In 2012, Jackson County Prosecutor Jean Peters Baker came to Ken Novak, chair of the Criminal Justice and Criminology Department, to ask how UMKC could help curb a rising tide of violence on Kansas City-area streets. She’d heard about focused deterrence and its success in other cities and wanted to try it here. It just so happened that Andrew Fox had just taken a job as a professor in UMKC’s criminology department, and Fox happened to have experience with focused deterrence.

The Application Of Machine Learning To Evidence Based Medicine

 

What if, bear with me now, what if the phase 3 clinical trials for mRNA therapeutics conducted on billions of unsuspecting, hoodwinked and bamboozled humans, was a new kind of research done to yield a new depth and breadth of clinical data exceptionally useful toward breaking up logjams in clinical terminology as well as experimental sample size? Vaxxed vs. Unvaxxed the subject of long term gubmint surveillance now. To what end?

Nature  | Recently, advances in wearable technologies, data science and machine learning have begun to transform evidence-based medicine, offering a tantalizing glimpse into a future of next-generation ‘deep’ medicine. Despite stunning advances in basic science and technology, clinical translations in major areas of medicine are lagging. While the COVID-19 pandemic exposed inherent systemic limitations of the clinical trial landscape, it also spurred some positive changes, including new trial designs and a shift toward a more patient-centric and intuitive evidence-generation system. In this Perspective, I share my heuristic vision of the future of clinical trials and evidence-based medicine.

Main

The last 30 years have witnessed breathtaking, unparalleled advancements in scientific research—from a better understanding of the pathophysiology of basic disease processes and unraveling the cellular machinery at atomic resolution to developing therapies that alter the course and outcome of diseases in all areas of medicine. Moreover, exponential gains in genomics, immunology, proteomics, metabolomics, gut microbiomes, epigenetics and virology in parallel with big data science, computational biology and artificial intelligence (AI) have propelled these advances. In addition, the dawn of CRISPR–Cas9 technologies has opened a tantalizing array of opportunities in personalized medicine.

Despite these advances, their rapid translation from bench to bedside is lagging in most areas of medicine and clinical research remains outpaced. The drug development and clinical trial landscape continues to be expensive for all stakeholders, with a very high failure rate. In particular, the attrition rate for early-stage developmental therapeutics is quite high, as more than two-thirds of compounds succumb in the ‘valley of death’ between bench and bedside^1,2. To bring a drug successfully through all phases of drug development into the clinic costs more than 1.5–2.5 billion dollars (refs. 3, 4). This, combined with the inherent inefficiencies and deficiencies that plague the healthcare system, is leading to a crisis in clinical research. Therefore, innovative strategies are needed to engage patients and generate the necessary evidence to propel new advances into the clinic, so that they may improve public health. To achieve this, traditional clinical research models should make way for avant-garde ideas and trial designs.

Before the COVID-19 pandemic, the conduct of clinical research had remained almost unchanged for 30 years and some of the trial conduct norms and rules, although archaic, were unquestioned. The pandemic exposed many of the inherent systemic limitations in the conduct of trials⁵ and forced the clinical trial research enterprise to reevaluate all processes—it has therefore disrupted, catalyzed and accelerated innovation in this domain^6,7. The lessons learned should help researchers to design and implement next-generation ‘patient-centric’ clinical trials.

Chronic diseases continue to impact millions of lives and cause major financial strain to society⁸, but research is hampered by the fact that most of the data reside in data silos. The subspecialization of the clinical profession has led to silos within and among specialties; every major disease area seems to work completely independently. However, the best clinical care is provided in a multidisciplinary manner with all relevant information available and accessible. Better clinical research should harness the knowledge gained from each of the specialties to achieve a collaborative model enabling multidisciplinary, high-quality care and continued innovation in medicine. Because many disciplines in medicine view the same diseases differently—for example, infectious disease specialists view COVID-19 as a viral disease while cardiology experts view it as an inflammatory one—cross-discipline approaches will need to respect the approaches of other disciplines. Although a single model may not be appropriate for all diseases, cross-disciplinary collaboration will make the system more efficient to generate the best evidence.

Over the next decade, the application of machine learning, deep neural networks and multimodal biomedical AI is poised to reinvigorate clinical research from all angles, including drug discovery, image interpretation, streamlining electronic health records, improving workflow and, over time, advancing public health (Fig. 1). In addition, innovations in wearables, sensor technology and Internet of Medical Things (IoMT) architectures offer many opportunities (and challenges) to acquire data⁹. In this Perspective, I share my heuristic vision of the future of clinical trials and evidence generation and deliberate on the main areas that need improvement in the domains of clinical trial design, clinical trial conduct and evidence generation.

Fig. 1: Timeline of drug development from the present to the future.

The figure represents the timeline from drug discovery to first-in-human phase 1 trials and ultimately FDA approval. Phase 4 studies occur after FDA approval and can go on for several years. There is an urgent need to reinvigorate clinical trials through drug discovery, interpreting imaging, streamlining electronic health records, and improving workflow, over time advancing public health. AI can aid in many of these aspects in all stages of drug development. DNN, deep neural network; EHR, electronic health records; IoMT, internet of medical things; ML, machine learning.

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Clinical trial design

Trial design is one of the most important steps in clinical research—better protocol designs lead to better clinical trial conduct and faster ‘go/no-go’ decisions. Moreover, losses from poorly designed, failed trials are not only financial but also societal.

Challenges with randomized controlled trials

Randomized controlled trials (RCTs) have been the gold standard for evidence generation across all areas of medicine, as they allow unbiased estimates of treatment effect without confounders. Ideally, every medical treatment or intervention should be tested via a well-powered and well-controlled RCT. However, conducting RCTs is not always feasible owing to challenges in generating evidence in a timely manner, cost, design on narrow populations precluding generalizability, ethical barriers and the time taken to conduct these trials. By the time they are completed and published, RCTs become quickly outdated and, in some cases, irrelevant to the current context. In the field of cardiology alone, 30,000 RCTs have not been completed owing to recruitment challenges¹⁰. Moreover, trials are being designed in isolation and within silos, with many clinical questions remaining unanswered. Thus, traditional trial design paradigms must adapt to contemporary rapid advances in genomics, immunology and precision medicine¹¹.

If True - THIS WOULD EXPLAIN SO MUCH!!!

Brownstone |  Contrary to popular belief that pharmaceutical companies drove the COVID vaccine development programs, the US FDA’s website (FDA, 2020) reveals that the United States Department of Defence (DoD) has been in full control of the Covid Vaccine development program since its beginning. The DoD has been responsible for development, manufacturing, clinical trials, quality assurance, distribution and administration, since that time (FDA, 2020; Rees and Latypova, 2022; KEI, 2022; Medical Defense Consortium, 2022; Rees, 2022). The major pharmaceutical companies have been involved as “Project Coordination Teams” effectively performing as subcontractors to the DoD. The Chief Operating Officer for the Warp Speed vaccine program is the US Department of Defence, and the Chief Science Advisor is the US Department of Health and Human Services (HHS). 

The Nature of Gene-based Vaccines

The true nature of the COVID-19 ‘vaccines’ has been largely misrepresented by mainstream media, big pharmaceutical companies and governments and is poorly understood by the population at large.  Referring to these products as “vaccines” led most people to consider them as relatively safe and well-researched and readily accept their widespread use. However, they are not really vaccines – they are serious gene-based interventions which have never been deployed widely in any population, especially never to healthy individuals including children, infants and pregnant women.  In this sense they should be considered experimental. 

COVID-19 ‘vaccines’ fall into a special class of therapeutic agents under the US FDA Office of Cellular, Tissue and Gene Therapies’ defined as “gene therapy products,” which involve “introducing a new or modified gene into the body to help treat a disease” (FDA, 2018). Heretofore, use of gene therapy products has been limited to the treatment of usually rare, serious and debilitating disease or genetic conditions. They have potential to cause permanent intergenerational genetic damage, cancer and interfere with reproductive capacity. 

The FDA and other drug regulatory agencies have specific rules and guidelines to direct manufacturers in development and testing of such products, for both preclinical (FDA, 2013) and clinical (FDA, 2015) research.  However, the FDA did not evaluate these COVID-19 “vaccines” according to these gene therapy guidelines.  

Instead, there was a concerted effort to avoid referring to them as gene therapy products, based, in part, on the argument that the genetic material in the COVID-19 vaccines was not intended to be incorporated into an individual’s DNA, nor to modify gene expression. There was no prior short-term safety information and no long-term data on which to predict future effects. No similar therapeutic products have been previously approved anywhere in the world.  Their widespread administration globally with no historical safety experience was an unprecedented risk in human health.        

Accelerating Development 

Messenger RNA platform technology has been researched by DARPA (Defense Advanced Projects Research Agency) since at least 2012 (McCullough, 2022).  In early 2020, in the panic to develop the COVID-19 vaccines, certain critical research and development procedures were omitted, bypassed, curtailed, or not done in a logical sequential manner, or to established laboratory or manufacturing standards. Although the spike protein is the active drug and is directly responsible for the immune response, its pharmacology and toxicology have not been studied in animals or in humans as would normally have been required. 

Other notable deficiencies include lack of critical research on carcinogenicity, mutagenicity, genotoxicity and reproductive toxicology in appropriate animal species. In particular, the potential for reverse transcription of mRNA genetic material into an individual’s DNA was not investigated. Furthermore, scale-up manufacturing was premature and lacked adequate quality control to ensure that product made in large batches is the same as made in smaller batches. 

Without such research, the potency, mRNA integrity, presence of contaminants and stability of the “vaccines” cannot be guaranteed. Such oversights are directly responsible for the failure to predict the serious adverse drug reactions and mortality which have now been reported in association with these vaccines. 

To mitigate risk, the plan in vaccine development was to use multiple technologies, multiple facilities and redundancy. Leverage of existing facilities would also take place. In the interest of expediency, the plan was to avoid using traditional pathways from early development to large-scale production.  Avoidance of quality standards and guidelines such as Good Manufacturing Practice and Good Laboratory Practice guidelines was necessary to speed development, and conventional New Drug Application (NDA) and Biologics License Application (BLA) approvals were bypassed. 

Instead, the process moved rapidly using compressed timelines and overlapping stages of development towards Emergency Use Authorization (EUA). Scale-up and large volume manufacturing was planned in parallel with, instead of before, clinical trials which, again, may have contravened accepted codes of Good Manufacturing Practices. These approaches were probably a recipe for potential disaster. (Latypova, 2022; Watt and Latypova, 2022).

How Can You Grant Amnesty To A Group That Still Has Its Boot On Your Neck?

newstarget  |  Three doctors in the armed forces have decided to blow the lid on the United States military’s open deception concerning the negative outcome of Wuhan coronavirus (Covid-19) “vaccination” on American troops.

According to the three whistleblowers, medical billing code data captured by the Defense Medical Epidemiology Database (DMED), which is run by the Department of Defense (DoD), shows that rates of miscarriage, myocarditis, cancer, Bell’s palsy, female infertility, and many other health conditions are up big time.

Cancer rates are particularly concerning, they say, as the normal average number of new cases per year is about 38,700, based on the time period from 2016-2020. In 2021 after Operation Warp Speed was launched, however, the number of new cancer cases that year rose to 114,645.

The Armed Forces Health Surveillance Branch (AFHSB) runs the DMED, which it describes as a “web-based tool to remotely query de-identified active component personnel and medical event data contained within the Defense Medical Surveillance System (DMSS).”

“The database contains every International Classification of Diseases (ICD) medical billing code for all medical diagnoses submitted by the military for medical insurance billing,” reports explain. (Related: Remember at the launch of Operation Warp Speed when Dr. Sara Beltrán Ponce, MD, suffered a horrific miscarriage right after getting jabbed for the Chinese Flu?)

Neurological issues up 1,000% in military following Operation Warp Speed

The three military whistleblowers in question are Samuel Sigoloff, Peter Chambers, and Theresa Long. Attorney Thomas Renz issued sworn statements from these three to the courts as part of a major lawsuit.

During the first 10 months of 2021, Renz says, miscarriages alone rose by 300 percent in the military. His hope is that the suit will lead to an end for covid jab mandates in the military.

Sen. Ron Johnson (R-Wisc.) is also involved, having recently hosted “COVID-19: A Second Opinion,” a livestreamed discussion panel featuring numerous world-renowned doctors and medical experts who offered a much different take on the scamdemic and how the government handled it.

On February 1 of this year, Johnson wrote a letter to U.S. Secretary of Defense Lloyd Austin. In it were the findings from a roundtable on covid jab injuries and deaths, including data showing a 10-fold increase in neurological issues post-Operation Warp Speed.

Johnson also revealed the following increases in other health conditions following the mandate of covid injections in the military:

• Hypertension: 2,181 percent increase
• Nervous system disorders: 1,048 percent increase
• Malignant neoplasms of esophagus: 894 percent increase
• Multiple sclerosis: 680 percent increase
• Malignant neoplasms of digestive organs: 624 percent increase
• Guillain-Barre syndrome: 551 percent increase
• Breast cancer: 487 percent increase
• Demyelinating: 487 percent increase
• Malignant neoplasms of thyroid and other endocrine glands: 474 percent increase
• Female infertility: 472 percent increase
• Pulmonary embolism: 468 percent increase
• Migraines: 452 percent increase
• Ovarian dysfunction: 437 percent increase
• Testicular cancer: 369 percent increase
• Tachycardia: 302 percent increase

Between the years of 2016 and 2020, there were 1,499 codes for miscarriage reported each year. From January through October 2021 – not even a full year – there were an astounding 4,182 miscarriages logged into the system.

 

Excess Deaths Soar To Higher Levels Than During The Panicdemic

telegraph  | Excess deaths in England and Wales are currently running higher than in the main pandemic years of 2020 and 2021, figures have shown.

Throughout October, there have been an average of 1,564 extra deaths per week, compared with a weekly average of just 315 in 2020 and 1,322 in 2021.

Latest figures from the Office for National Statistics (ONS) showed that in the week ending Oct 21, there were 1,714 excess deaths in England and Wales, of which only 469 were due to Covid - just 27 per cent of the total. 

It is 16.8 per cent higher than normal. Deaths are also running higher than the five-year pre-Covid October average from 2015 to 2019, figures showed.

Health experts have warned that some of the unexplained deaths are being caused by collateral damage from the pandemic, when operations and treatments were cancelled or delayed as the health service concentrated on Covid.

The Government’s “stay at home, protect the NHS” message also left many people who needed medical treatment unwilling to bother the health service, or afraid they would catch coronavirus if they went into hospital.

The NHS is also struggling from long-term staffing issues and current shortages because of coronavirus, leading to record waits for ambulances, treatment and surgery. 

Dr Charles Levinson, of the private GP service DoctorCall, which has seen a rise in patients presenting with advanced conditions, said: “What is driving the excess death crisis? In my view, delays in diagnosis/treatment now and throughout the pandemic. 

“The reasons behind this are clearly up for debate. I also believe that the Government needs to be far more open on this and tell us what they are doing to solve it.”

 

The Billions In Profit Are Conspicuously Obvious, But Seriously Folks Pfizer Jes Phukkin With Y'all...,

dailymail |  Joe Biden has been re-infected with COVID after taking an anti-viral drug that leaves patients running a 40 per cent risk of flare-up of the virus shortly afterwards.

Taking Paxlovid leaves COVID sufferers in danger of testing positive for the virus again very quickly after clearing their initial infection. 

When Paxlovid came to market in December 2021, studies from Pfizer indicated that only 1-2 percent of patients who took the drug tested positive for Covid again shortly after finishing their dosage. 

But other experts say the rapid reinfection rate is closer to 40 per cent, and that Paxlovid can cause this issue by suppressing patients' immune systems too early, meaning their own bodies are unable to get a handle on COVID.  

Dr. Jonathan Reiner, a prominent cardiologist and professor of medicine and surgery at George Washington University Hospital tweeted: 'I think this was predictable.'

He continued: 'The prior data suggesting 'rebound' Paxlovid positivity in the low single digits is outdates and with BA.5 is likely 20-40% or even higher.'

In a memo released by the White House, Dr. Kevin O'Connor said that the president will continue to isolate, just like he did when he first tested positive on July 21. 

Dr. O'Connor also said that the president would not be prescribed Paxlovid again. The president's doctor earlier noted that it was likely that the president was infected with the BA.5 variant. 

In June, a Mayo Clinic study showed that five percent of adults who had taken the drug tested positive again for Covid within 30 days, according to the New York Times. 

The majority of those who experienced rebound symptoms occur within two to eight days.  

Some experts have said that the current treatment cycle of taking three pills twice a day for five days is too short a time period to clear Covid from the patient's body. 

The conclusion of the Mayo Clinic study was that extending the time period of the course of Paxlovid was unnecessary. 

The authors of the study conceded in their findings that immunocompromised people were unrepresented in the study.  

Also in June, the president's chief medical advisor, Dr. Anthony Fauci, experienced rebound Covid-19. In his case, he did take a second round of Paxlovid. 

Dr. Ashish K. Jha, the White House’s Covid-19 response coordinator, has denied that the Paxlovid rebound numbers are nearly 50 percent. 

The doctor maintained that the actual percentage of reinfections is 'in the single digits.'

Dr. Jha said: 'When people have rebound, they don’t end up in the hospital. They don’t end up particularly sick.' 

He added: 'Paxlovid is working really well at preventing serious illness, rebound or no rebound, and that’s why he was offered it. And that’s why the president took it.

HUGE Food For Thought As They Start Dispensing Newfangled Pox Jabs

amidwesterndoctor |  This is a supplemental addition to my previous piece.  I would strongly encourage you to read that article before reading this one as this one goes into more tangential and complex points that supplement the original, but many of you may find very insightful.  Many of the concepts here also appear to apply to the COVID immunizations, however for length considerations, I will omit most of those connections and leave you to draw your own conclusions.  All of the books I cited here can be easily found on Amazon and often as PDFs, but I avoided linking to them here and supporting Amazon. Lastly, as I did not want to further delay publication, a significant number of minor edits will occur in the next few days.

I did not expect to attract the viewership the original article received, or the follow-up by larger media outlets (Steve Kirsch’s newsletter, the Kate Daley show and mercola.com) and am sincerely grateful for your support, and those parties in particular in spreading this message.  As I now have many readers, I will try to produce quality content as my time permits (with work and all), as I want it to be worth your time to read what I produce.  For the time being I will focus on interesting bits of medical history (the next piece will be interesting lessons from the 1918 influenza I applied to my treatment of COVID).

Additionally, since my last publication a reader notified me of a short book written in 1889 and viewable online which concisely provides evidence for many of the points covered in Dissolving Illusions, such as the lack of efficacy from the vaccination, the diseases associated with its administration, the distortion of data used by government officials to claim benefit rather than harm, and false claim it reduced death in hospitals.

To be complete and illustrate the observed effects of the smallpox vaccines, this article is a bit longer than the previous.  I could have cited significantly more resources, but I aimed to cover one text that was representative from each major school of thought at the time.  Its sections are as follows:

-Introduction
-General Smallpox Observations
-Allopathy
-Naturopathy
-Homeopathy
-Osteopathy
-Traditional Chinese Medicine
-Modern Research

Immune Tolerance Is One Reason Repeated mRNA Jabs And Boosters Kill

igorchudov  |  Now, for June-July, we see that more boosters mean MORE deaths and that the association between booster rates and Covid deaths is highly statistically significant!

This is the Best “Apples-to-Apples” Comparison

Let’s summarize. We looked at the same set of countries in Europe during three different periods of time. During the first period, booster rates were associated with statistically significant reductions in Covid deaths. During the second period, booster rates had no effect on Covid death rates. And during the last, third period, booster rates CONTRIBUTED to greater deaths!

The fact that all three periods involved the same countries (except a couple who did not report booster rates during the first period), means that this outcome is NOT due to population-wide age or other demographic differences. The difference between outcomes in these periods is due to the passage of time, and changes in the interaction of boosted immune systems with the evolving virus.

Note that my data shows something much worse than “boosters stopping to work”. Instead of merely becoming useless, like in the second period, boosters became harmful and promoted deaths in the third period.

Immune Tolerance due to Boosters

Why is this happening? Boosters and vaccines worsening Covid outcomes is really a topic for another article to explore possible answers.

There are certainly MANY REASONS why boosters do not work anymore. Let me touch upon just one such reason. Remember that other reasons are also important!

Jan Ashton describes the “immune phenomenon known as tolerance”. What “tolerance” means is that repeated antigen injections end up working like allergy shots, increasing tolerance to the antigen, which is in this case spike protein.

Tolerance towards allergens, like tree pollen, is a good thing. (I had allergy shots myself). However, tolerance toward a replicating virus that damages our cardiovascular system and immune system, is a bad thing! Tolerance also turns affected people into walking Covid superspreaders.

Instead of seeing the viral antigen as a sign to start a battle against the virus, the immune system says “oh well, another spike protein injection” and ignores it. That allows the virus to multiply unchecked and cause immense damage by killing various cells and hurting our cardiovascular systems and more. The infected person feels less fever and less disturbance than they would feel from a robust immune reaction, so the illness feels “milder”, but this is actually a bad thing because the virus multiplies unopposed.

More Shady Connections Than Hunter Biden And Jeffrey Epstein Combined...,

Click on the image below to watch the video on Bitchute.

Meet Nathan Wolfe (5 mins)

expose-news  |   Dr. Nathan Wolfe was a founding citizen of Ghislaine Maxwell’s TerraMar Project; a member of the Edge Foundation; a self-proclaimed “virus hunter” whose area of research is zoonotic diseases with a special focus on bats; with links to the Wuhan Institute of Virology and EcoHealth Alliance; who previously bungled epidemic responses while selling pandemic insurance; whose company Metabiota which is funded by Rosemont Seneca, Google, The Skoll Foundation, among others, was awarded a sub-contract with the US Military’s DTRA program for work in Ukrainian biolabs.

A few days before the end of March Russian Foreign Ministry spokeswoman Marija Zakharova published a timeline of US-Ukraine bioresearch headed “BioBiden.”  Of the 23 timeline points she listed, Nathan Wolfe or organisations associated with him – Metabiota and Global Viral – were explicitly mentioned in 8 of them:

• 2007 – US DoD employee Nathan Wolfe founded Global Viral Forecasting Institute (subsequently – Global Viral), a biomedical company. The mission stated in the charter is non-commercial study of transborder infections, including in China.
• 2014 – Metabiota, a private commercial organisation specialising in the study of pandemic risks is detached from Global Viral. Neil Callahan and John DeLoche, employees of Hunter Biden’s company Rosemont Seneca Partners are appointed to the board of Metabiota. Global Viral and Metabiota begin to get funding from the US Department of Defence.
• 2014 – Metabiota shows interest in Ukraine and invites Hunter Biden to “assert Ukraine’s cultural & economic independence from Russia”.
• 2014 – Metabiota and Burisma Holdings begin cooperation on an unnamed “science project in Ukraine”.
• 2014 – Metabiota, Global Viral and Black & Veatch Special Projects begin full-fledged cooperation within the US DoD programmes.
• 2014-2016 – Implementation of Metabiota and US DoD contracts, including a $300,000 project in Ukraine.
• 2016 – former US Assistant Secretary for Defence Andrew Weber is appointed head of Metabiota’s global partnerships department.
• 2016 – EcoHealth Alliance, a Global Viral founder Nathan Wolfe’s structure, is engaged in the study of bat-transmitted coronaviruses at the research centre in a Wuhan laboratory, China.

Considering the accusation is US political elites’ involvement in the military biological activity in Ukraine, it perhaps indicates Moscow has identified Nathan Wolfe as a person of interest in what Zakharova termed “this truly diabolical plan.”

Read more: Russian Foreign Ministry Releases Alleged “BioBiden” Timeline of US Bioresearch in Ukraine, The Gateway Pundit, 29 March 2022

Meet Nathan Wolfe

“If an alien visited Earth, they would take some note of humans, but probably spend most of their time trying to understand the dominant form of life on our planet –microorganisms like bacteria and viruses.”

Nathan Wolfe, Business Continuity and The Pandemic Threat Robert A Clark (2016)

From 1999 to 2006 Wolfe conducted research as a postdoctoral student and then as an assistant professor at Johns Hopkins University.  There he worked with American epidemiologist Donald Burke, who suspected that the practice of hunting bushmeat in Africa had exposed a source of HIV. Based in Cameroon, Wolfe studied the local hunters and their hunting practices.  In 2004 he and his colleagues found that 1% of bushmeat hunters were infected with the simian foamy virus – a virus that is closely related to HIV and carried by nonhuman primates.

In 2006 he joined the department of epidemiology at the University of California, Los Angeles. He began pursuing ways to monitor, predict, and prevent animal-to-human transfer of viruses and conducted projects in Africa and Southeast Asia. In China, he collaborated with scientists to investigate wet markets (food markets that sell live animals) as a source of zoonoses (diseases from wild animals).

Read more: Nathan Wolfe, Britannica

Before Its Ukraine Skullduggery - Metabiota Had A Hand In Ebola Outbreaks In Africa

thesaker.is |  The Ministry of Defence of the Russian Federation continues analysing the military-biological activity of the USA and its allies in Ukraine and other regions of the world in view of new information received at the liberated territories and at the branch offices of the Defence Threat Reduction Agency (DTRA) that form a unified information network.

We have previously stated that the Ukrainian project of the Pentagon do not meet the pertinent healthcare problems of Ukraine, while their implementation has not led to any improvement of the sanitary-epidemiological situation.

The special military operation has led to forming the final report on DTRA activity dated from 2005 to 2016.

The document contains the data on evaluation of healthcare, veterinary and biosecurity system efficiency prepared by a group of U.S. experts in 2016.

This report is a concept document designed for further planification of military-biological activity of the Pentagon in Ukraine that contains conclusions on implementation of the programme guidelines.

Despite the more than 10-year-long period of cooperation in the alleged '...reduction of biological threats...', the experts have stated:

'...There is no legislation on the control of highly dangerous pathogens in the country, there are significant deficiencies in biosafety... The current state of resources makes it impossible for laboratories to respond effectively to public health emergencies...'

The document emphasises that '...over the past five years, Ukraine has shown no progress in implementing international health regulations of the World Health Organisation'.

The report pays particular attention to non-compliance with biosafety requirements when working and storing microbial collections.

It has been stated '...that most facilities are characterised by numerous gross violations, such as unlocked fencing systems, unlatching windows, broken or inactive pathogen restriction systems, lack of alarm systems...' The results of the review conclude that there is no system for protecting dangerous pathogens in Ukraine.

At the same time, the activities of the Defence Threat Reduction Agency (DTRA) have been assessed positively: the organisation has managed to bring the national collection of microorganisms to the United States, to organise biological assessment work and to implement projects to study particularly dangerous and economically significant infections that could cause a worsening (changing) epidemic situation.

The report makes the case for continuing this work on behalf of the Pentagon that has cost more than $250 million since 2005.

The document is annexed with ambiguous comments about the sponsors and implementers of the Biological Threat Reduction Programme in Ukraine that have nothing to do with biosecurity issues. In particular, the Soros Foundation is mentioned with the notation '...contributed to the development of an open and democratic society...'

It confirms again that the official activities of the Pentagon in Ukraine are just a front for illegal military and biological research.

We have repeatedly mentioned the role of U.S. Democratic Party representatives in funding bioweapons activities in Ukraine and the intermediary organisations that have been used for this purpose.

I would like to refer to one of the key Pentagon contractors receiving money from Hunter Biden's investment fund, Metabiota.

The available data suggests that the company is merely a front for internationally dubious purposes and is used by the U.S. political elite to carry out opaque financial activities in various parts of the world.

There is a specific example: Metabiota was involved in the response to the Ebola epidemic in West Africa. The activities of the company's employees have raised questions from the World Health Organisation (WHO) in terms of their compliance with biosafety requirements.

This is the report of the international panel of experts from the Haemorrhagic Fever Consortium who were involved in the fight against Ebola virus disease in Sierra Leone in 2015.

According to the document, Metabiota staff had failed to comply with handling procedures and concealed the involvement of Pentagon staff who were using the company as a front. The main purpose of these activities was to isolate highly virulent variants of the virus from sick and dead people, as well as to export its strains to the USA.

In view of the apparent failure of Metabiota's activities to meet the goals of controlling the spread of the disease, the World Health Organisation's Ebola coordinator, Philippe Barbosa, recommended to recall the staff of the company saying he was extremely concerned about the potential risks of such collaboration to WHO's reputation.

The U.S. military contractor's heightened interest in the Ebola virus is not a coincidence: the disease is one of the most pathogenic to humans. During the outbreak that began in 2014, 28,000 people were contaminated, over 11,000 of them died, the mortality rate was around 40%.

The special military operation has led to receiving documents that reveals the plans of Metabiota and the Ukrainian Scientific-Technological Centre to study the Ebola virus in Ukraine.

This is the request for U.S. funding to diagnose highly dangerous pathogens in Ukraine, including Ebola virus. This kind of requests are part of U.S. strategy to redeploy high-risk work with dangerous pathogens to third countries.

The research was to be carried out at the Mechnikov Anti-Plague Institute in Odessa. As the disease is not endemic and has never been recorded in Ukraine indeed, there is a legitimate question about the need for such research and its true purpose.

We have already noted that Ukraine and other post-Soviet states have become a testing ground for biological weapons not only for the USA, but also for its NATO allies; on the first place, Germany. Various projects have been carried out on behalf of the Joint Medical Service of the German Armed Forces.

Bundeswehr professionals paid particular attention to the Congo-Crimean fever pathogen. A large-scale screening of the susceptibility of the local population to this infection was carried out and included summarising demographic, epidemiological and clinical data. This kind of approaches allows to identify new regional virus genotypes and to select strains that cause latent clinical forms.

The study of natural foci of Crimean-Congo fever was carried out under the pretext of improving the Ukrainian epidemiological surveillance system, with the participation of the Institute of Veterinary Medicine in Kiev and the Mechnikov Anti-Plague Institute in Odessa.

Bundeswehr's interest in Crimean-Congo fever stems from the fact that mortality can be as high as 30% and its outbreaks create a need for lengthy and costly treatment, preventive and special handling measures.

This is a quote from Bundeswehr's instructions: '...pay particular attention to fatal cases of infection with Crimean-Congo fever as it allows the virus strains with maximum pathogenicity and virulence for humans to be extracted from the dead individuals...'

Apart from Germany, microbiologists from the USA have shown a keen interest in tick-borne infections; research in this area has been funded by DTRA through the UP-1 and UP-8 projects.

A separate project on ixodid ticks that are vectors of a number of highly dangerous infections (tularemia, West Nile fever, Congo-Crimean fever) has been implemented by the University of Texas.

Ticks used to be collected in the south-eastern regions of Ukraine, where natural foci of infections characteristic of the territory of the Russian Federation are located. At the same time, the period of implementing this work coincided with a rapid increase in the incidence of tick-borne borreliosis among the Ukrainian population, as well as the increase in the number of ticks in various regions of Russia bordering Ukraine.

This issue is being studied by competent Russian professionals in coordination with professionals from the Ministry of Defence of Russia.

We have previously pointed out the significance of the results of the military-biological projects codenamed UP for the Pentagon.

Note the report prepared for the U.S. Defence Department by Black & Veatch and Metabiota. According to the document, Veterinary Projects codenamed 'TAP' were implemented simultaneously with the UP projects in Ukraine.

Their main guideline lies in economically significant quarantine infections capable of damaging the agriculture of several countries and entire regions, such as glanders, African swine fever (ASF), classical swine fever, highly pathogenic avian influenza and Newcastle disease.

African swine fever with two projects dedicated to this pathogen represented particular interest to U.S. military biologists.

The TAP-3 project was aimed to study the spread of ASF pathogen through wild animals. The migration routes of wild boar through Ukraine had been examining within its framework. The TAP-6 project scaled this process up to Eastern European countries.

The study of vector populations of dangerous zoonotic infections was carried out by staff of the Institute of New Pathogens of the University of Florida (Gainesville) in Volyn, Rovno, Zhitomir and Chernigov regions of Ukraine, as well as in the areas bordering Belarus and Russia.

Note the worsening situation of African swine fever in Eastern European countries: According to the International Office of Epizootics, since 2014, outbreaks have been recorded in Latvia (4,021 cases), Estonia (3,814) and Lithuania (4,201). In Poland, more than 13,000 cases of ASF have been detected, and agricultural losses from the disease have exceeded 2.4 billion euro.

We have already emphasised the use of biological weapons in Cuba in the 1970s and 1980s. Today, I would like to focus on U.S. military-biological activities during the Korean War.

In March 2022, the U.S. Army Strategic Studies Institute published a report on the U.S. chemical and biological weapons programme during the Korean War. This report was aimed to create a possible line of defence against allegations of illegal activities carried out by U.S. biolaboratories in Ukraine.

The document attempts to refute the testimony of 38 U.S. military pilots who have admitted using biological weapons in China and Korea.

According to the document, while preparing for the Korean campaign, '...the U.S. Air Force secured additional funds to purchase large quantities of chemical and biological munitions, obtained a testing range for them in Canada and carried out an extensive conceptual work on their use...'

At that time, the Americans considered brucellosis pathogens and economically important infections, including wheat stem rust, as priority biological agents. 2,500 munitions of this type the U.S. Air Force Strategic Air Command planned to use, including '...to attack Soviet grain crops...'

Analysis of the data mentioned in the report shows that the U.S. command uses the results of the research received from the Japanese military-biological programme and a certain 'continuity' of the works previously carried out by the Detachment 731 led by Shiro Ishii.

This is the record of the closed session of CIA, State Department and the Pentagon representatives dated July 7, 1953. The document clearly shows that the Americans are focusing on techniques to manipulate public opinion and launch an aggressive counter-attack within their strategies aimed to defend from allegations.

The report states that the officials are reluctant to actual investigations of chemical and biological incidents due to fears of revealing the activities carried out by the U.S. Eighth Army.

Thus, the comparative analysis of U.S. activities during the Korean War and currently in Ukraine demonstrates the persistence of the U.S. policy of building up its own military and biological capabilities in circumvention of international agreements.

In conclusion, I would like to present real data on the health condition of the voluntarily surrendered Ukrainian servicemen. This diapositive presents the data on presence of antibodies to contagious disease agents without mentioning personal data of these servicemen.

The results are as follows: 33% of the examined servicemen had had hepatitis A, over 4% had renal syndrome fever and 20% had West Nile fever. The figures are significantly higher than the statistical average. In view of active research of these diseases held by the Pentagon within the Ukrainian projects, there is reason to believe that servicemen of the Armed Forces of Ukraine (AFU) were involved as volunteers in experiments to assess the tolerance of dangerous infectious diseases.

The lack of therapeutic effect of antibacterial medication has been reported during in-patient treatment of AFU servicemen in medical facilities. High concentrations of antibiotics, including sulphonyl amides and fluoroquinolones, have been detected in their blood.

This fact may indicate preventive use of antibiotics and preparation of personnel for operating in conditions of biological contamination, such as cholera agent, that indirectly proves the information of the Russian Defence Ministry that Ukrainian special units were planning to use biological agents.

The data will be included in the U.S. military-biological dossier and we will continue to examine it and keep you informed.