Smoking gun: Fauci states COVID PCR test has fatal flaw; confession from the “beloved” expert of experts

The COVID PCR test is a complete fraud

by Jon Rappoport

December 8, 2021

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As my readers know, I’ve been proving for well over a year that the SARS-CoV-2 virus doesn’t exist.

Therefore, any test for it would be absurd.

However, I frequently put on my hazmat suit and enter the crazy world where all “the experts” claim the virus is real. I make these forays to show that, even within their fantasy bubble, and by their own standards, the pros are fatally contradicting themselves and lying constantly.

That’s what I’m doing in this article. I’ve got my hazmat suit on and I’m exploring the crazy landscape. I’ve published this piece several times, but I want to make sure people understand how the test has been used to manufacture the false appearance of a pandemic.

OK, here we go. Smoking gun. Jackpot.

Right from the horse’s mouth. Right from the man we’re told is the number-one COVID expert in the nation. What Fauci says is golden truth.

Well, how about THIS?

July 16, 2020, podcast, “This Week in Virology”: Tony Fauci makes a point of saying the PCR COVID test is useless and misleading when the test is run at “35 cycles or higher.” A positive result, indicating infection, cannot be accepted or believed.

Here, in techno-speak, is an excerpt from Fauci’s key quote (starting at the 4m01s mark through to the 5m45s mark (Fauci begins his first answer to the first question at the 4m20s mark and begins his second answer to the second question at the 5m26s mark)):

“…If you get [perform the test at] a cycle threshold of 35 or more…the chances of it being replication-competent [aka accurate] are miniscule…you almost never can culture virus [detect a true positive result] from a 37 threshold cycle…even 36…”

Each “cycle” of the test is a quantum leap in amplification and magnification of the test specimen taken from the patient.

Too many cycles, and the test will turn up all sorts of irrelevant material that will be wrongly interpreted as relevant.

That’s called a false positive.

What Fauci failed to say on the video is: the FDA, which authorizes the test for public use, recommends the test should be run up to 40 cycles. Not 35.

Therefore, all labs in the US following the FDA guideline are knowingly or unknowingly participating in fraud. Fraud on a monstrous level, because…

Millions of Americans are being told they are infected with the virus on the basis of a false positive result, and…

The total number of COVID cases in America—which is based on the test—is a gross falsity.

The lockdowns and other restraining measures are based on these fraudulent case numbers.

Let me back up and run that by you again. Fauci says the test is useless when it’s run at 35 cycles or higher. The FDA says run the test up to 40 cycles, in order to determine whether the virus is there. This is the crime in a nutshell.

“Hello, America, you’ve been tricked, lied to, conned, and taken for a devastating ride. On the basis of fake science, the country was locked down.”

If anyone in the Congress has a few brain cells operating, pull Fauci into a televised hearing and, in ten minutes, make mincemeat out of the fake science that has driven this whole foul, stench-ridden assault on the global economy and its 8 billion citizens.

All right, here are two chunks of evidence for what I’ve written above. First, we have a CDC quote on the FDA website, in a document titled: “CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel For Emergency Use Only.” This document is marked, “Effective: 07/13/20.” That means, even though the virus is being referred to by its older name, the document is still relevant as of July 2020. “For Emergency Use Only” refers to the fact that the FDA has certified the PCR test under a traditional category called “Emergency Use Authorization.”

FDA: “…a specimen is considered positive for 2019-nCoV [virus] if all 2019-nCoV marker (N1, N2) cycle threshold growth curves cross the threshold line within 40.00 cycles ([less than] 40.00 Ct).”

Naturally, testing labs reading this guideline would conclude, “Well, to see if the virus is there in a patient, we should run the test all the way to 40 cycles. That’s the official advice.”

Then we have a New York Times article (August 29/updated September 17, 2020) headlined: “Your coronavirus test is positive. Maybe it shouldn’t be.” Here are money quotes:

“Most tests set the limit at 40 [cycles]. A few at 37.”

“Set-the-limit” would mean, We’re going to look all the way to 40 cycles, to see if the virus is there.

The Times: “This number of amplification cycles needed to find the virus, called the cycle threshold, is never included in the results sent to doctors and coronavirus patients.”

Boom. That’s the capper, the grand finale. Labs don’t or won’t reveal their collusion in this crime.

Get the picture?

I hope so.

If a lawyer won’t go to court with all this, or if a judge won’t pay attention and see the light, they should be stripped of their jobs and sent to the Arctic to sell snow.

2021 CODA: Recently, Florida, a state which has remained far more open and free from COVID restrictions and mandates than most other states, is reporting very low COVID case numbers. Why?

Because as of December 3, 2020, the state of Florida started doing something unheard of. It demanded that labs report the number of cycles (“cycle threshold”) for every test they run.

Here is the relevant wording in a release from the Florida governor, Ron DeSantis, and the state Department of Health:

“Cycle threshold (CT) values and their reference ranges, as applicable, must be reported by laboratories to FDOH via electronic laboratory reporting or by fax immediately.”

“If your laboratory is not currently reporting CT values and their reference ranges, the lab should begin reporting this information to FDOH within seven days of the date of this memorandum.”

We can assume there is only one reason for this order. The Florida governor and the Department of Health are aware that tests run at 35 cycles or higher are useless and misleading, creating a mountain of false-positives, and they want to stop this crime.

And with the Governor’s recent appointment of a new state Surgeon General, who is well aware of certain aspects of the COVID fraud, the requirement for labs to start telling the truth is taking hold.

Hence, lower case numbers.


SOURCES:

youtu.be/a_Vy6fgaBPE?t=241

blog.nomorefakenews.com/tag/pcr/

https://www.fda.gov/media/134922/download (document page 35 (pdf page 36), “CDC 2019-Novel Coronavirus (2019-nCoV), Real-Time RT-PCR Diagnostic Panel, For Emergency Use Only, Instructions for Use, Catalog # 2019-nCoVEUA-01, 1000 reactions, For In-vitro Diagnostic (IVD) Use, Rx Only”; CDC-006-00019, Revision: 07 CDC/DDID/NCIRD/ Division of Viral Diseases, Effective: 07/21/2021)

nytimes.com/2020/08/29/health/coronavirus-testing.html

blog.nomorefakenews.com/2021/08/24/gov-ron-desantis-this-is-how-you-win-against-the-wolves/


The Matrix Revealed

(To read about Jon’s mega-collection, The Matrix Revealed, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

Pfizer smoking-gun secret document: their deadly COVID vaccine

Awakening from the trance

by Jon Rappoport

December 7, 2021

(To join our email list, click here.)

CORRECTION: After publishing this article, I discovered that the gigantic Pfizer list of medical conditions was apparently not a report on logged cases of adverse events, but instead a complete list of conditions that Pfizer would be monitoring, in order to see whether they popped up on their radar as reactions to the COVID vaccine.

Why would Pfizer publish this extraordinary list? Because as they state, these medical conditions have been associated with severe COVID-19 “and vaccines in general.” In other words, vaccines in general, historically, have carried enormous risk and dangers over an incredibly wide area of medical conditions. This is a key confession.

Further, if you read the full secret Pfizer document, you will come to Table 7, which does list a number of categories of adverse reactions, all of which WERE reported in the first three months of the Pfizer vaccine rollout. This IS stunning.

In the secret document, Pfizer does list 1,223 deaths occurring after just three months of the vaccine rollout. This should have been sufficient to cause a complete halt to the vaccination program.

Finally, Pfizer admits that in the first three months of the vaccine rollout, it logged a staggering 42,086 cases of adverse reactions. And as far as I can determine from the Pfizer document, these 42,086 cases represented a total of 139,888 adverse events. In other words, in many cases, there were reports of multiple adverse events.


Journalist Celia Farber just wrote an explosive article on the Pfizer secret document. You should read it (and her addendum, here). She deserves our thanks and gratitude. And here you can also read the document itself.

In short, the Pfizer document (which was never supposed to see the light of day but was disclosed as part of a FOIA suit) describes the adverse effects from just the first three months of injections with the company’s COVID vaccine:

158,000 adverse events, 1,223 deaths. In a half-sane world, this would have been more than enough to halt all injections and cancel the vaccine.

I’ve queried two attorneys. They both looked at the Pfizer document and state they believe it’s authentic.

The appendix of the Pfizer document is the most astonishing section. It’s beyond astonishing. It lists all the types of vaccine adverse events Pfizer logged—again, in just three months of injections.

Page after page after page after page of types of adverse events. Each type of event cast in medical language, the language of the dead. The proponents of this technical-ese speak, as it were, from beyond the grave. They’re super-educated brainwashed zombies. It’s as if they’re listing and counting abstractions in an academic board game.

The abstractions raise no concerns. In the document, no one is waving red flags. They’re all medical bean counters, keeping their books with precision.

Make no mistake, these are the people who are operating the levers of society on a day-to-day basis, maiming and killing with a confident attitude that indicates they are beyond reproach. The very notion of reproach is foreign to them.

Civilization is drowning. It’s drowning in a giant lake of TECHNIQUE. The uses to which technique is put have become irrelevant. Just follow procedure. Carry out assigned tasks. Pass along information. Report on results. And then you will have achieved immunity from blame.

Or resist and rebel no matter what. These are the stakes. This is the war.

Get ready. Buckle up. Logged by Pfizer, covering the first three months of COVID vaccination, here is the corporation’s list of types of vaccine adverse events, as published by Celia Farber:


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5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports

APPENDIX 1. LIST OF ADVERSE EVENTS OF SPECIAL INTEREST

1p36 deletion syndrome; 2-Hydroxyglutaric aciduria; 5’nucleotidase increased; Acoustic neuritis; Acquired C1 inhibitor deficiency; Acquired epidermolysis bullosa; Acquired epileptic aphasia; Acute cutaneous lupus erythematosus; Acute disseminated encephalomyelitis; Acute encephalitis with refractory, repetitive partial seizures; Acute febrile neutrophilic dermatosis; Acute flaccid myelitis; Acute haemorrhagic leukoencephalitis; Acute haemorrhagic oedema of infancy; Acute kidney injury; Acute macular outer retinopathy; Acute motor axonal neuropathy; Acute motor-sensory axonal neuropathy; Acute myocardial infarction; Acute respiratory distress syndrome [Note by Celia Farber: “that sounds like ‘Covid 19’.”]; Acute respiratory failure; Addison’s disease; Administration site thrombosis; Administration site vasculitis; Adrenal thrombosis; Adverse event following immunisation; Ageusia; Agranulocytosis; Air embolism; Alanine aminotransferase abnormal; Alanine aminotransferase increased; Alcoholic seizure; Allergic bronchopulmonary mycosis; Allergic oedema; Alloimmune hepatitis; Alopecia areata; Alpers disease; Alveolar proteinosis; Ammonia abnormal; Ammonia increased; Amniotic cavity infection; Amygdalohippocampectomy; Amyloid arthropathy; Amyloidosis; Amyloidosis senile; Anaphylactic reaction; Anaphylactic shock; Anaphylactic transfusion reaction; Anaphylactoid reaction; Anaphylactoid shock; Anaphylactoid syndrome of pregnancy; Angioedema; Angiopathic neuropathy; Ankylosing spondylitis; Anosmia; Antiacetylcholine receptor antibody positive; Anti-actin antibody positive; Anti-aquaporin-4 antibody positive; Anti-basal ganglia antibody positive; Anti-cyclic citrullinated peptide antibody positive; Anti-epithelial antibody positive; Anti-erythrocyte antibody positive; Anti-exosome complex antibody positive; Anti- GAD antibody negative; Anti-GAD antibody positive; Anti-ganglioside antibody positive; Antigliadin antibody positive; Anti-glomerular basement membrane antibody positive; Anti-glomerular basement membrane disease; Anti-glycyl-tRNA synthetase antibody positive; Anti-HLA antibody test positive; Anti-IA2 antibody positive; Anti-insulin antibody increased; Anti-insulin antibody positive; Anti-insulin receptor antibody increased; Anti-insulin receptor antibody positive; Anti-interferon antibody negative; Anti-interferon antibody positive; Anti-islet cell antibody positive; Antimitochondrial antibody positive; Anti-muscle specific kinase antibody positive; Anti-myelin-associated glycoprotein antibodies positive; Anti-myelin-associated glycoprotein associated polyneuropathy; Antimyocardial antibody positive; Anti-neuronal antibody positive; Antineutrophil cytoplasmic antibody increased; Antineutrophil cytoplasmic antibody positive; Anti-neutrophil cytoplasmic antibody positive vasculitis; Anti-NMDA antibody positive; Antinuclear antibody increased; Antinuclear antibody positive; Antiphospholipid antibodies positive; Antiphospholipid syndrome; Anti-platelet antibody positive; Anti-prothrombin antibody positive; Antiribosomal P antibody positive; Anti-RNA polymerase III antibody positive; Anti-saccharomyces cerevisiae antibody test positive; Anti-sperm antibody positive; Anti-SRP antibody positive; Antisynthetase syndrome; Anti-thyroid antibody positive; Anti-transglutaminase antibody increased; Anti-VGCC antibody positive; Anti-VGKC antibody positive; Anti-vimentin antibody positive; Antiviral prophylaxis; Antiviral treatment; Anti-zinc transporter 8 antibody positive; Aortic embolus; Aortic thrombosis; Aortitis; Aplasia pure red cell; Aplastic anaemia; Application site thrombosis; Application site vasculitis; Arrhythmia; Arterial bypass occlusion; Arterial bypass thrombosis; Arterial thrombosis; Arteriovenous fistula thrombosis; Arteriovenous graft site stenosis; Arteriovenous graft thrombosis; Arteritis; Arteritis

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5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports

[con’t] [Arteritis] coronary; Arthralgia; Arthritis; Arthritis enteropathic; Ascites; Aseptic cavernous sinus thrombosis; Aspartate aminotransferase abnormal; Aspartate aminotransferase increased; Aspartate-glutamate-transporter deficiency; AST to platelet ratio index increased; AST/ALT ratio abnormal; Asthma; Asymptomatic COVID-19; Ataxia; Atheroembolism; Atonic seizures; Atrial thrombosis; Atrophic thyroiditis; Atypical benign partial epilepsy; Atypical pneumonia [Note by Celia Farber: “This sounds like the original definition of Covid-19 out of Wuhan.”]; Aura; Autoantibody positive; Autoimmune anaemia; Autoimmune aplastic anaemia; Autoimmune arthritis; Autoimmune blistering disease; Autoimmune cholangitis; Autoimmune colitis; Autoimmune demyelinating disease; Autoimmune dermatitis; Autoimmune disorder; Autoimmune encephalopathy; Autoimmune endocrine disorder; Autoimmune enteropathy; Autoimmune eye disorder; Autoimmune haemolytic anaemia; Autoimmune heparin-induced thrombocytopenia; Autoimmune hepatitis; Autoimmune hyperlipidaemia; Autoimmune hypothyroidism; Autoimmune inner ear disease; Autoimmune lung disease; Autoimmune lymphoproliferative syndrome; Autoimmune myocarditis; Autoimmune myositis; Autoimmune nephritis; Autoimmune neuropathy; Autoimmune neutropenia; Autoimmune pancreatitis; Autoimmune pancytopenia; Autoimmune pericarditis; Autoimmune retinopathy; Autoimmune thyroid disorder; Autoimmune thyroiditis; Autoimmune uveitis; Autoinflammation with infantile enterocolitis; Autoinflammatory disease; Automatism epileptic; Autonomic nervous system imbalance; Autonomic seizure; Axial spondyloarthritis; Axillary vein thrombosis; Axonal and demyelinating polyneuropathy; Axonal neuropathy; Bacterascites; Baltic myoclonic epilepsy; Band sensation; Basedow’s disease; Basilar artery thrombosis; Basophilopenia; B-cell aplasia; Behcet’s syndrome; Benign ethnic neutropenia; Benign familial neonatal convulsions; Benign familial pemphigus; Benign rolandic epilepsy; Beta-2 glycoprotein antibody positive; Bickerstaff’s encephalitis; Bile output abnormal; Bile output decreased; Biliary ascites; Bilirubin conjugated abnormal; Bilirubin conjugated increased; Bilirubin urine present; Biopsy liver abnormal; Biotinidase deficiency; Birdshot chorioretinopathy; Blood alkaline phosphatase abnormal; Blood alkaline phosphatase increased; Blood bilirubin abnormal; Blood bilirubin increased; Blood bilirubin unconjugated increased; Blood cholinesterase abnormal; Blood cholinesterase decreased; Blood pressure decreased; Blood pressure diastolic decreased; Blood pressure systolic decreased; Blue toe syndrome; Brachiocephalic vein thrombosis; Brain stem embolism; Brain stem thrombosis; Bromosulphthalein test abnormal; Bronchial oedema; Bronchitis; Bronchitis mycoplasmal; Bronchitis viral; Bronchopulmonary aspergillosis allergic; Bronchospasm; Budd- Chiari syndrome; Bulbar palsy; Butterfly rash; C1q nephropathy; Caesarean section; Calcium embolism; Capillaritis; Caplan’s syndrome; Cardiac amyloidosis; Cardiac arrest; Cardiac failure; Cardiac failure acute; Cardiac sarcoidosis; Cardiac ventricular thrombosis; Cardiogenic shock; Cardiolipin antibody positive; Cardiopulmonary failure; Cardio-respiratory arrest; Cardio-respiratory distress; Cardiovascular insufficiency; Carotid arterial embolus; Carotid artery thrombosis; Cataplexy; Catheter site thrombosis; Catheter site vasculitis; Cavernous sinus thrombosis; CDKL5 deficiency disorder; CEC syndrome; Cement embolism; Central nervous system lupus; Central nervous system vasculitis; Cerebellar artery thrombosis; Cerebellar embolism; Cerebral amyloid angiopathy; Cerebral arteritis; Cerebral artery embolism; Cerebral artery thrombosis; Cerebral gas embolism; Cerebral microembolism; Cerebral septic infarct; Cerebral thrombosis; Cerebral venous sinus thrombosis; Cerebral venous thrombosis; Cerebrospinal thrombotic

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5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports

[con’t] [Cerebrospinal thrombotic] tamponade; Cerebrovascular accident; Change in seizure presentation; Chest discomfort; Child- Pugh-Turcotte score abnormal; Child-Pugh-Turcotte score increased; Chillblains; Choking; Choking sensation; Cholangitis sclerosing; Chronic autoimmune glomerulonephritis; Chronic cutaneous lupus erythematosus; Chronic fatigue syndrome; Chronic gastritis; Chronic inflammatory demyelinating polyradiculoneuropathy; Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids; Chronic recurrent multifocal osteomyelitis; Chronic respiratory failure; Chronic spontaneous urticaria; Circulatory collapse; Circumoral oedema; Circumoral swelling; Clinically isolated syndrome; Clonic convulsion; Coeliac disease; Cogan’s syndrome; Cold agglutinins positive; Cold type haemolytic anaemia; Colitis; Colitis erosive; Colitis herpes; Colitis microscopic; Colitis ulcerative; Collagen disorder; Collagen-vascular disease; Complement factor abnormal; Complement factor C1 decreased; Complement factor C2 decreased; Complement factor C3 decreased; Complement factor C4 decreased; Complement factor decreased; Computerised tomogram liver abnormal; Concentric sclerosis; Congenital anomaly; Congenital bilateral perisylvian syndrome; Congenital herpes simplex infection; Congenital myasthenic syndrome; Congenital varicella infection; Congestive hepatopathy; Convulsion in childhood; Convulsions local; Convulsive threshold lowered; Coombs positive haemolytic anaemia; Coronary artery disease; Coronary artery embolism; Coronary artery thrombosis; Coronary bypass thrombosis; Coronavirus infection; Coronavirus test; Coronavirus test negative; Coronavirus test positive; Corpus callosotomy; Cough; Cough variant asthma; COVID-19; COVID-19 immunisation; COVID-19 pneumonia; COVID-19 prophylaxis; COVID-19 treatment; Cranial nerve disorder; Cranial nerve palsies multiple; Cranial nerve paralysis; CREST syndrome; Crohn’s disease; Cryofibrinogenaemia; Cryoglobulinaemia; CSF oligoclonal band present; CSWS syndrome; Cutaneous amyloidosis; Cutaneous lupus erythematosus; Cutaneous sarcoidosis; Cutaneous vasculitis; Cyanosis; Cyclic neutropenia; Cystitis interstitial; Cytokine release syndrome; Cytokine storm; De novo purine synthesis inhibitors associated acute inflammatory syndrome; Death neonatal; Deep vein thrombosis; Deep vein thrombosis postoperative; Deficiency of bile secretion; Deja vu; Demyelinating polyneuropathy; Demyelination; Dermatitis; Dermatitis bullous; Dermatitis herpetiformis; Dermatomyositis; Device embolisation; Device related thrombosis; Diabetes mellitus; Diabetic ketoacidosis; Diabetic mastopathy; Dialysis amyloidosis; Dialysis membrane reaction; Diastolic hypotension; Diffuse vasculitis; Digital pitting scar; Disseminated intravascular coagulation; Disseminated intravascular coagulation in newborn; Disseminated neonatal herpes simplex; Disseminated varicella; Disseminated varicella zoster vaccine virus infection; Disseminated varicella zoster virus infection; DNA antibody positive; Double cortex syndrome; Double stranded DNA antibody positive; Dreamy state; Dressler’s syndrome; Drop attacks; Drug withdrawal convulsions; Dyspnoea; Early infantile epileptic encephalopathy with burst-suppression; Eclampsia; Eczema herpeticum; Embolia cutis medicamentosa; Embolic cerebellar infarction; Embolic cerebral infarction; Embolic pneumonia; Embolic stroke; Embolism; Embolism arterial; Embolism venous; Encephalitis; Encephalitis allergic; Encephalitis autoimmune; Encephalitis brain stem; Encephalitis haemorrhagic; Encephalitis periaxialis diffusa; Encephalitis post immunisation; Encephalomyelitis; Encephalopathy; Endocrine disorder; Endocrine ophthalmopathy; Endotracheal intubation; Enteritis; Enteritis leukopenic; Enterobacter pneumonia; Enterocolitis; Enteropathic spondylitis; Eosinopenia; Eosinophilic

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5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports

[con’t] [Eosinophilic] fasciitis; Eosinophilic granulomatosis with polyangiitis; Eosinophilic oesophagitis; Epidermolysis; Epilepsy; Epilepsy surgery; Epilepsy with myoclonic-atonic seizures; Epileptic aura; Epileptic psychosis; Erythema; Erythema induratum; Erythema multiforme; Erythema nodosum; Evans syndrome; Exanthema subitum; Expanded disability status scale score decreased; Expanded disability status scale score increased; Exposure to communicable disease; Exposure to SARS-CoV-2; Eye oedema; Eye pruritus; Eye swelling; Eyelid oedema; Face oedema; Facial paralysis; Facial paresis; Faciobrachial dystonic seizure; Fat embolism; Febrile convulsion; Febrile infection-related epilepsy syndrome; Febrile neutropenia; Felty’s syndrome; Femoral artery embolism; Fibrillary glomerulonephritis; Fibromyalgia; Flushing; Foaming at mouth; Focal cortical resection; Focal dyscognitive seizures; Foetal distress syndrome; Foetal placental thrombosis; Foetor hepaticus; Foreign body embolism; Frontal lobe epilepsy; Fulminant type 1 diabetes mellitus; Galactose elimination capacity test abnormal; Galactose elimination capacity test decreased; Gamma-glutamyltransferase abnormal; Gamma-glutamyltransferase increased; Gastritis herpes; Gastrointestinal amyloidosis; Gelastic seizure; Generalised onset non-motor seizure; Generalised tonic-clonic seizure; Genital herpes; Genital herpes simplex; Genital herpes zoster; Giant cell arteritis; Glomerulonephritis; Glomerulonephritis membranoproliferative; Glomerulonephritis membranous; Glomerulonephritis rapidly progressive; Glossopharyngeal nerve paralysis; Glucose transporter type 1 deficiency syndrome; Glutamate dehydrogenase increased; Glycocholic acid increased; GM2 gangliosidosis; Goodpasture’s syndrome; Graft thrombosis; Granulocytopenia; Granulocytopenia neonatal; Granulomatosis with polyangiitis; Granulomatous dermatitis; Grey matter heterotopia; Guanase increased; Guillain- Barre syndrome; Haemolytic anaemia; Haemophagocytic lymphohistiocytosis; Haemorrhage; Haemorrhagic ascites; Haemorrhagic disorder; Haemorrhagic pneumonia; Haemorrhagic varicella syndrome; Haemorrhagic vasculitis; Hantavirus pulmonary infection; Hashimoto’s encephalopathy; Hashitoxicosis; Hemimegalencephaly; Henoch-Schonlein purpura; Henoch- Schonlein purpura nephritis; Hepaplastin abnormal; Hepaplastin decreased; Heparin-induced thrombocytopenia; Hepatic amyloidosis; Hepatic artery embolism; Hepatic artery flow decreased; Hepatic artery thrombosis; Hepatic enzyme abnormal; Hepatic enzyme decreased; Hepatic enzyme increased; Hepatic fibrosis marker abnormal; Hepatic fibrosis marker increased; Hepatic function abnormal; Hepatic hydrothorax; Hepatic hypertrophy; Hepatic hypoperfusion; Hepatic lymphocytic infiltration; Hepatic mass; Hepatic pain; Hepatic sequestration; Hepatic vascular resistance increased; Hepatic vascular thrombosis; Hepatic vein embolism; Hepatic vein thrombosis; Hepatic venous pressure gradient abnormal; Hepatic venous pressure gradient increased; Hepatitis; Hepatobiliary scan abnormal; Hepatomegaly; Hepatosplenomegaly; Hereditary angioedema with C1 esterase inhibitor deficiency; Herpes dermatitis; Herpes gestationis; Herpes oesophagitis; Herpes ophthalmic; Herpes pharyngitis; Herpes sepsis; Herpes simplex; Herpes simplex cervicitis; Herpes simplex colitis; Herpes simplex encephalitis; Herpes simplex gastritis; Herpes simplex hepatitis; Herpes simplex meningitis; Herpes simplex meningoencephalitis; Herpes simplex meningomyelitis; Herpes simplex necrotising retinopathy; Herpes simplex oesophagitis; Herpes simplex otitis externa; Herpes simplex pharyngitis; Herpes simplex pneumonia; Herpes simplex reactivation; Herpes simplex sepsis; Herpes simplex viraemia; Herpes simplex virus conjunctivitis neonatal; Herpes simplex visceral; Herpes virus

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[con’t] [Herpes virus] infection; Herpes zoster; Herpes zoster cutaneous disseminated; Herpes zoster infection neurological; Herpes zoster meningitis; Herpes zoster meningoencephalitis; Herpes zoster meningomyelitis; Herpes zoster meningoradiculitis; Herpes zoster necrotising retinopathy; Herpes zoster oticus; Herpes zoster pharyngitis; Herpes zoster reactivation; Herpetic radiculopathy; Histone antibody positive; Hoigne’s syndrome; Human herpesvirus 6 encephalitis; Human herpesvirus 6 infection; Human herpesvirus 6 infection reactivation; Human herpesvirus 7 infection; Human herpesvirus 8 infection; Hyperammonaemia; Hyperbilirubinaemia; Hypercholia; Hypergammaglobulinaemia benign monoclonal; Hyperglycaemic seizure; Hypersensitivity; Hypersensitivity vasculitis; Hyperthyroidism; Hypertransaminasaemia; Hyperventilation; Hypoalbuminaemia; H ypocalcaemic seizure; Hypogammaglobulinaemia; Hypoglossal nerve paralysis; Hypoglossal nerve paresis; Hypoglycaemic seizure; Hyponatraemic seizure; Hypotension; Hypotensive crisis; Hypothenar hammer syndrome; Hypothyroidism; Hypoxia; Idiopathic CD4 lymphocytopenia [Note by Celia Farber: “sounds like ‘AIDS’ except Fauci re-defined AIDS in 1993, after the ‘Amsterdam Surprise’ as only occurring when HIV was ‘present’ so all thousands the non HIV, ‘idiopathic CD4 lympho-cytopenia’ cases were excluded, creating a tautological definition that came to be ‘HIV/AIDS’.”]; Idiopathic generalised epilepsy; Idiopathic interstitial pneumonia; Idiopathic neutropenia; Idiopathic pulmonary fibrosis; IgA nephropathy; IgM nephropathy; IIIrd nerve paralysis; IIIrd nerve paresis; Iliac artery embolism; Immune thrombocytopenia; Immune- mediated adverse reaction; Immune-mediated cholangitis; Immune-mediated cholestasis; Immune-mediated cytopenia; Immune-mediated encephalitis; Immune-mediated encephalopathy; Immune-mediated endocrinopathy; Immune-mediated enterocolitis; Immune- mediated gastritis; Immune-mediated hepatic disorder; Immune-mediated hepatitis; Immune- mediated hyperthyroidism; Immune-mediated hypothyroidism; Immune-mediated myocarditis; Immune-mediated myositis; Immune-mediated nephritis; Immune-mediated neuropathy; Immune-mediated pancreatitis; Immune-mediated pneumonitis; Immune-mediated renal disorder; Immune-mediated thyroiditis; Immune-mediated uveitis; Immunoglobulin G4 related disease; Immunoglobulins abnormal; Implant site thrombosis; Inclusion body myositis; Infantile genetic agranulocytosis; Infantile spasms; Infected vasculitis; Infective thrombosis; Inflammation; Inflammatory bowel disease; Infusion site thrombosis; Infusion site vasculitis; Injection site thrombosis; Injection site urticaria; Injection site vasculitis; Instillation site thrombosis; Insulin autoimmune syndrome; Interstitial granulomatous dermatitis; Interstitial lung disease; Intracardiac mass; Intracardiac thrombus; Intracranial pressure increased; Intrapericardial thrombosis; Intrinsic factor antibody abnormal; Intrinsic factor antibody positive; IPEX syndrome; Irregular breathing; IRVAN syndrome; IVth nerve paralysis; IVth nerve paresis; JC polyomavirus test positive; JC virus CSF test positive; Jeavons syndrome; Jugular vein embolism; Jugular vein thrombosis; Juvenile idiopathic arthritis; Juvenile myoclonic epilepsy; Juvenile polymyositis; Juvenile psoriatic arthritis; Juvenile spondyloarthritis; Kaposi sarcoma inflammatory cytokine syndrome; Kawasaki’s disease; Kayser-Fleischer ring; Keratoderma blenorrhagica; Ketosis- prone diabetes mellitus; Kounis syndrome; Lafora’s myoclonic epilepsy; Lambl’s excrescences; Laryngeal dyspnoea; Laryngeal oedema; Laryngeal rheumatoid arthritis; Laryngospasm; Laryngotracheal oedema; Latent autoimmune diabetes in adults; LE cells present; Lemierre syndrome; Lennox-Gastaut syndrome; Leucine aminopeptidase increased; Leukoencephalomyelitis; Leukoencephalopathy; Leukopenia; Leukopenia neonatal; Lewis-Sumner syndrome; Lhermitte’s sign; Lichen planopilaris; Lichen planus; Lichen sclerosus; Limbic encephalitis; Linear IgA disease; Lip oedema; Lip swelling; Liver function test abnormal; Liver function test decreased; Liver function test increased; Liver induration; Liver injury; Liver iron concentration abnormal; Liver iron concentration

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5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports

[con’t] [Liver iron concentration] increased; Liver opacity; Liver palpable; Liver sarcoidosis; Liver scan abnormal; Liver tenderness; Low birth weight baby; Lower respiratory tract herpes infection; Lower respiratory tract infection; Lower respiratory tract infection viral; Lung abscess; Lupoid hepatic cirrhosis; Lupus cystitis; Lupus encephalitis; Lupus endocarditis; Lupus enteritis; Lupus hepatitis; Lupus myocarditis; Lupus myositis; Lupus nephritis; Lupus pancreatitis; Lupus pleurisy; Lupus pneumonitis; Lupus vasculitis; Lupus-like syndrome; Lymphocytic hypophysitis; Lymphocytopenia neonatal; Lymphopenia; MAGIC syndrome; Magnetic resonance imaging liver abnormal; Magnetic resonance proton density fat fraction measurement; Mahler sign; Manufacturing laboratory analytical testing issue; Manufacturing materials issue; Manufacturing production issue; Marburg’s variant multiple sclerosis; Marchiafava-Bignami disease; Marine Lenhart syndrome; Mastocytic enterocolitis; Maternal exposure during pregnancy; Medical device site thrombosis; Medical device site vasculitis; MELAS syndrome; Meningitis; Meningitis aseptic; Meningitis herpes; Meningoencephalitis herpes simplex neonatal; Meningoencephalitis herpetic; Meningomyelitis herpes; MERS-CoV test; MERS-CoV test negative; MERS-CoV test positive; Mesangioproliferative glomerulonephritis; Mesenteric artery embolism; Mesenteric artery thrombosis; Mesenteric vein thrombosis; Metapneumovirus infection; Metastatic cutaneous Crohn’s disease; Metastatic pulmonary embolism; Microangiopathy; Microembolism; Microscopic polyangiitis; Middle East respiratory syndrome; Migraine-triggered seizure; Miliary pneumonia; Miller Fisher syndrome; Mitochondrial aspartate aminotransferase increased; Mixed connective tissue disease; Model for end stage liver disease score abnormal; Model for end stage liver disease score increased; Molar ratio of total branched-chain amino acid to tyrosine; Molybdenum cofactor deficiency; Monocytopenia; Mononeuritis; Mononeuropathy multiplex; Morphoea; Morvan syndrome; Mouth swelling; Moyamoya disease; Multifocal motor neuropathy; Multiple organ dysfunction syndrome; Multiple sclerosis; Multiple sclerosis relapse; Multiple sclerosis relapse prophylaxis; Multiple subpial transection; Multisystem inflammatory syndrome in children; Muscular sarcoidosis; Myasthenia gravis; Myasthenia gravis crisis; Myasthenia gravis neonatal; Myasthenic syndrome; Myelitis; Myelitis transverse; Myocardial infarction; Myocarditis; Myocarditis post infection; Myoclonic epilepsy; Myoclonic epilepsy and ragged-red fibres; Myokymia; Myositis; Narcolepsy; Nasal herpes; Nasal obstruction; Necrotising herpetic retinopathy; Neonatal Crohn’s disease; Neonatal epileptic seizure; Neonatal lupus erythematosus; Neonatal mucocutaneous herpes simplex; Neonatal pneumonia; Neonatal seizure; Nephritis; Nephrogenic systemic fibrosis; Neuralgic amyotrophy; Neuritis; Neuritis cranial; Neuromyelitis optica pseudo relapse; Neuromyelitis optica spectrum disorder; Neuromyotonia; Neuronal neuropathy; Neuropathy peripheral; Neuropathy, ataxia, retinitis pigmentosa syndrome; Neuropsychiatric lupus; Neurosarcoidosis; Neutropenia; Neutropenia neonatal; Neutropenic colitis; Neutropenic infection; Neutropenic sepsis; Nodular rash; Nodular vasculitis; Noninfectious myelitis; Noninfective encephalitis; Noninfective encephalomyelitis; Noninfective oophoritis; Obstetrical pulmonary embolism; Occupational exposure to communicable disease; Occupational exposure to SARS-CoV-2; Ocular hyperaemia; Ocular myasthenia; Ocular pemphigoid; Ocular sarcoidosis; Ocular vasculitis; Oculofacial paralysis; Oedema; Oedema blister; Oedema due to hepatic disease; Oedema mouth; Oesophageal achalasia; Ophthalmic artery thrombosis; Ophthalmic herpes simplex; Ophthalmic herpes zoster; Ophthalmic vein thrombosis; Optic neuritis; Optic

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BNT162b2

5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports

[con’t] [Optic] neuropathy; Optic perineuritis; Oral herpes; Oral lichen planus; Oropharyngeal oedema; Oropharyngeal spasm; Oropharyngeal swelling; Osmotic demyelination syndrome; Ovarian vein thrombosis; Overlap syndrome; Paediatric autoimmune neuropsychiatric disorders associated with streptococcal infection; Paget-Schroetter syndrome; Palindromic rheumatism; Palisaded neutrophilic granulomatous dermatitis; Palmoplantar keratoderma; Palpable purpura; Pancreatitis; Panencephalitis; Papillophlebitis; Paracancerous pneumonia; Paradoxical embolism; Parainfluenzae viral laryngotracheobronchitis; Paraneoplastic dermatomyositis; Paraneoplastic pemphigus; Paraneoplastic thrombosis; Paresis cranial nerve; Parietal cell antibody positive; Paroxysmal nocturnal haemoglobinuria; Partial seizures; Partial seizures with secondary generalisation; Patient isolation; Pelvic venous thrombosis; Pemphigoid; Pemphigus; Penile vein thrombosis; Pericarditis; Pericarditis lupus; Perihepatic discomfort; Periorbital oedema; Periorbital swelling; Peripheral artery thrombosis; Peripheral embolism; Peripheral ischaemia; Peripheral vein thrombus extension; Periportal oedema; Peritoneal fluid protein abnormal; Peritoneal fluid protein decreased; Peritoneal fluid protein increased; Peritonitis lupus; Pernicious anaemia; Petit mal epilepsy; Pharyngeal oedema; Pharyngeal swelling; Pityriasis lichenoides et varioliformis acuta; Placenta praevia; Pleuroparenchymal fibroelastosis; Pneumobilia; Pneumonia; Pneumonia adenoviral; Pneumonia cytomegaloviral; Pneumonia herpes viral; Pneumonia influenzal; Pneumonia measles; Pneumonia mycoplasmal; Pneumonia necrotising; Pneumonia parainfluenzae viral; Pneumonia respiratory syncytial viral; Pneumonia viral; POEMS syndrome; Polyarteritis nodosa; Polyarthritis; Polychondritis; Polyglandular autoimmune syndrome type I; Polyglandular autoimmune syndrome type II; Polyglandular autoimmune syndrome type III; Polyglandular disorder; Polymicrogyria; Polymyalgia rheumatica; Polymyositis; Polyneuropathy; Polyneuropathy idiopathic progressive; Portal pyaemia; Portal vein embolism; Portal vein flow decreased; Portal vein pressure increased; Portal vein thrombosis; Portosplenomesenteric venous thrombosis; Post procedural hypotension; Post procedural pneumonia; Post procedural pulmonary embolism; Post stroke epilepsy; Post stroke seizure; Post thrombotic retinopathy; Post thrombotic syndrome; Post viral fatigue syndrome; Postictal headache; Postictal paralysis; Postictal psychosis; Postictal state; Postoperative respiratory distress; Postoperative respiratory failure; Postoperative thrombosis; Postpartum thrombosis; Postpartum venous thrombosis; Postpericardiotomy syndrome; Post-traumatic epilepsy; Postural orthostatic tachycardia syndrome; Precerebral artery thrombosis; Pre-eclampsia; Preictal state; Premature labour; Premature menopause; Primary amyloidosis; Primary biliary cholangitis; Primary progressive multiple sclerosis; Procedural shock; Proctitis herpes; Proctitis ulcerative; Product availability issue; Product distribution issue; Product supply issue; Progressive facial hemiatrophy; Progressive multifocal leukoencephalopathy; Progressive multiple sclerosis; Progressive relapsing multiple sclerosis; Prosthetic cardiac valve thrombosis; Pruritus; Pruritus allergic; Pseudovasculitis; Psoriasis; Psoriatic arthropathy; Pulmonary amyloidosis; Pulmonary artery thrombosis; Pulmonary embolism; Pulmonary fibrosis; Pulmonary haemorrhage; Pulmonary microemboli; Pulmonary oil microembolism; Pulmonary renal syndrome; Pulmonary sarcoidosis; Pulmonary sepsis; Pulmonary thrombosis; Pulmonary tumour thrombotic microangiopathy; Pulmonary vasculitis; Pulmonary veno-occlusive disease; Pulmonary venous thrombosis; Pyoderma gangrenosum; Pyostomatitis vegetans; Pyrexia; Quarantine; Radiation leukopenia; Radiculitis

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BNT162b2

5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports

[con’t] [Radiculitis] brachial; Radiologically isolated syndrome; Rash; Rash erythematous; Rash pruritic; Rasmussen encephalitis; Raynaud’s phenomenon; Reactive capillary endothelial proliferation; Relapsing multiple sclerosis; Relapsing-remitting multiple sclerosis; Renal amyloidosis; Renal arteritis; Renal artery thrombosis; Renal embolism; Renal failure; Renal vascular thrombosis; Renal vasculitis; Renal vein embolism; Renal vein thrombosis; Respiratory arrest; Respiratory disorder; Respiratory distress; Respiratory failure; Respiratory paralysis; Respiratory syncytial virus bronchiolitis; Respiratory syncytial virus bronchitis; Retinal artery embolism; Retinal artery occlusion; Retinal artery thrombosis; Retinal vascular thrombosis; Retinal vasculitis; Retinal vein occlusion; Retinal vein thrombosis; Retinol binding protein decreased; Retinopathy; Retrograde portal vein flow; Retroperitoneal fibrosis; Reversible airways obstruction; Reynold’s syndrome; Rheumatic brain disease; Rheumatic disorder; Rheumatoid arthritis; Rheumatoid factor increased; Rheumatoid factor positive; Rheumatoid factor quantitative increased; Rheumatoid lung; Rheumatoid neutrophilic dermatosis; Rheumatoid nodule; Rheumatoid nodule removal; Rheumatoid scleritis; Rheumatoid vasculitis; Saccadic eye movement; SAPHO syndrome; Sarcoidosis; SARS-CoV-1 test; SARS-CoV-1 test negative; SARS-CoV-1 test positive; SARS-CoV-2 antibody test; SARS-CoV-2 antibody test negative; SARS-CoV-2 antibody test positive; SARS-CoV-2 carrier; SARS-CoV-2 sepsis; SARS-CoV-2 test; SARS- CoV-2 test false negative; SARS-CoV-2 test false positive; SARS-CoV-2 test negative; SARS- CoV-2 test positive; SARS-CoV-2 viraemia; Satoyoshi syndrome; Schizencephaly; Scleritis; Sclerodactylia; Scleroderma; Scleroderma associated digital ulcer; Scleroderma renal crisis; Scleroderma-like reaction; Secondary amyloidosis; Secondary cerebellar degeneration; Secondary progressive multiple sclerosis; Segmented hyalinising vasculitis; Seizure; Seizure anoxic; Seizure cluster; Seizure like phenomena; Seizure prophylaxis; Sensation of foreign body; Septic embolus; Septic pulmonary embolism; Severe acute respiratory syndrome; Severe myoclonic epilepsy of infancy; Shock; Shock symptom; Shrinking lung syndrome; Shunt thrombosis; Silent thyroiditis; Simple partial seizures; Sjogren’s syndrome; Skin swelling; SLE arthritis; Smooth muscle antibody positive; Sneezing; Spinal artery embolism; Spinal artery thrombosis; Splenic artery thrombosis; Splenic embolism; Splenic thrombosis; Splenic vein thrombosis; Spondylitis; Spondyloarthropathy; Spontaneous heparin-induced thrombocytopenia syndrome; Status epilepticus; Stevens-Johnson syndrome [Note by Celia Farber: “This, SJS, can result in the skin coming off the body altogether, from the body’s attempt to rid itself of poison.”]; Stiff leg syndrome; Stiff person syndrome; Stillbirth; Still’s disease; Stoma site thrombosis; Stoma site vasculitis; Stress cardiomyopathy; Stridor; Subacute cutaneous lupus erythematosus; Subacute endocarditis; Subacute inflammatory demyelinating polyneuropathy; Subclavian artery embolism; Subclavian artery thrombosis; Subclavian vein thrombosis; Sudden unexplained death in epilepsy; Superior sagittal sinus thrombosis; Susac’s syndrome; Suspected COVID- 19; Swelling; Swelling face; Swelling of eyelid; Swollen tongue; Sympathetic ophthalmia; Systemic lupus erythematosus; Systemic lupus erythematosus disease activity index abnormal; Systemic lupus erythematosus disease activity index decreased; Systemic lupus erythematosus disease activity index increased; Systemic lupus erythematosus rash; Systemic scleroderma; Systemic sclerosis pulmonary; Tachycardia; Tachypnoea; Takayasu’s arteritis; Temporal lobe epilepsy; Terminal ileitis; Testicular autoimmunity; Throat tightness; Thromboangiitis obliterans; Thrombocytopenia; Thrombocytopenic purpura; Thrombophlebitis; Thrombophlebitis migrans; Thrombophlebitis

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BNT162b2

5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports

[con’t] [Thrombophlebitis] neonatal; Thrombophlebitis septic; Thrombophlebitis superficial; Thromboplastin antibody positive; Thrombosis; Thrombosis corpora cavernosa; Thrombosis in device; Thrombosis mesenteric vessel; Thrombotic cerebral infarction; Thrombotic microangiopathy; Thrombotic stroke; Thrombotic thrombocytopenic purpura; Thyroid disorder; Thyroid stimulating immunoglobulin increased; Thyroiditis; Tongue amyloidosis; Tongue biting; Tongue oedema; Tonic clonic movements; Tonic convulsion; Tonic posturing; Topectomy; Total bile acids increased; Toxic epidermal necrolysis; Toxic leukoencephalopathy; Toxic oil syndrome; Tracheal obstruction; Tracheal oedema; Tracheobronchitis; Tracheobronchitis mycoplasmal; Tracheobronchitis viral; Transaminases abnormal; Transaminases increased; Transfusion-related alloimmune neutropenia; Transient epileptic amnesia; Transverse sinus thrombosis; Trigeminal nerve paresis; Trigeminal neuralgia; Trigeminal palsy; Truncus coeliacus thrombosis; Tuberous sclerosis complex; Tubulointerstitial nephritis and uveitis syndrome; Tumefactive multiple sclerosis; Tumour embolism; Tumour thrombosis; Type 1 diabetes mellitus; Type I hypersensitivity; Type III immune complex mediated reaction; Uhthoff’s phenomenon; Ulcerative keratitis; Ultrasound liver abnormal; Umbilical cord thrombosis; Uncinate fits; Undifferentiated connective tissue disease; Upper airway obstruction; Urine bilirubin increased; Urobilinogen urine decreased; Urobilinogen urine increased; Urticaria; Urticaria papular; Urticarial vasculitis; Uterine rupture; Uveitis; Vaccination site thrombosis; Vaccination site vasculitis; Vagus nerve paralysis; Varicella; Varicella keratitis; Varicella post vaccine; Varicella zoster gastritis; Varicella zoster oesophagitis; Varicella zoster pneumonia; Varicella zoster sepsis; Varicella zoster virus infection; Vasa praevia; Vascular graft thrombosis; Vascular pseudoaneurysm thrombosis; Vascular purpura; Vascular stent thrombosis; Vasculitic rash; Vasculitic ulcer; Vasculitis; Vasculitis gastrointestinal; Vasculitis necrotising; Vena cava embolism; Vena cava thrombosis; Venous intravasation; Venous recanalisation; Venous thrombosis; Venous thrombosis in pregnancy; Venous thrombosis limb; Venous thrombosis neonatal; Vertebral artery thrombosis; Vessel puncture site thrombosis; Visceral venous thrombosis; VIth nerve paralysis; VIth nerve paresis; Vitiligo; Vocal cord paralysis; Vocal cord paresis; Vogt-Koyanagi-Harada disease; Warm type haemolytic anaemia; Wheezing; White nipple sign; XIth nerve paralysis; X-ray hepatobiliary abnormal; Young’s syndrome; Zika virus associated Guillain Barre syndrome.

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—Unless we rebel, someday this list will be engraved on a large memorial, and it will be framed in positive language, as an unparalleled achievement, as the introduction to the new genetically engineered human race.


power outside the matrix

(To read about Jon’s collection, Power Outside The Matrix, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

Test for new Omicron variant? We don’t need no stinkin’ test

by Jon Rappoport

December 2, 2021

(To join our email list, click here.)

This is an article in three layers. I’ve already spelled out the first layer in my current series on the Omicron variant of SARS-CoV-2 (archive: Omicron).

In a nutshell, there is no Omicron because there is no SARS-CoV-2. The “pandemic virus” doesn’t exist. A variation of nothing equals nothing.

However, I often make forays into the bubble-world where most people, including “the experts,” believe the virus is real. I do this to show that, within their world, the experts are constantly lying in their own terms and contradicting themselves.

Within their world, you would think the pros have an easily accessible test to identify the new Omicron variant in thousands or millions of people. Otherwise, how can they claim it’s here and spreading?

But you would be wrong.

And I have the evidence, based on the prior variant, the Delta. That’s level two. I take you there now, with an article I wrote months ago:

—Bombshell: PCR tests can’t identify Delta Variant; it’s all fiction—

Oooo. The Delta Variant. It’s everywhere. (archive: Delta)

Watch out. It’s under your rug. It’s in the clothes closet. It’s on your toothbrush.

And it’s The Unvaccinated who are spreading it. Those devils. We, who are pure, must be protected from the unvaxxed Unclean.

Fauci, god of soccer moms, rises every morning saying DELTA, goes on television saying DELTA, and goes to sleep praying to DELTA.

But read this from the Texas Department of State Health Services FAQ: “How can I tell if I have the Delta variant? Do labs report that to the state?” That information may not be readily available. The [PCR] viral tests that are used to determine if a person has COVID-19 are not designed to tell you what variant is causing the infection. Detecting the Delta variant, or other variants, requires a special type of testing called genomic sequencing. Due to the volume of COVID-19 cases, sequencing is not performed on all viral samples. However, because the Delta variant now accounts for the majority of COVID-19 cases in the United States, there is a strong likelihood that a positive test result indicates infection with the Delta variant.”

Boom.

I can assure you, the number of patients whose samples are genetically sequenced is tiny, contrasted against the number whose samples are simply run through the standard PCR.

So there is no way to know that the Delta variant now accounts for the majority of COVID cases in the US. And using the standard PCR, there is no way to know ANY specific patient has the Delta. It’s all fiction.

We have this from the American Lung Association: “Regular COVID-19 tests do not detect which variant is involved in a patient’s case—that information does not change the approach to care or therapy. The variant identification requires genomic sequencing, a process separate from regular virus tests and one that not all labs are able to do or do not do on a routine basis for patient care but are done more for public health monitoring.”

Let me break down how this game works. To be excessively generous, let’s say that 3 out of every 1000 positive PCR tests in America are sent to high-level labs, where genetic sequencing is done.

A certain percentage of THOSE sequencing tests come up positive for the Delta Variant. Based on these results, MODELS are constructed.

Now we’re REALLY into fake science. The models estimate what percentage of ALL positive PCR tests are really positive for Delta.

I’m sorry to break this newsflash, but modelers are notorious charlatans. Their dense calculations are as far from science as a Model-T Ford is from a spaceship.

But based on models, public health agencies—who desperately needed a new con, because COVID case numbers were declining—blasted through their media assets the new revelation: THE DELTA MONSTER IS LOOSE AMONG US.

But it gets even worse. Why? Because you can bet the farm that the current model pushing the omnipresence of the Delta Variant was never challenged. It was never handed to several groups of independent scientists who went over it with a fine-toothed comb. That’s called verification. That’s called the Scientific Method. You may have heard of it.

The most notorious modeler in the world, Neil Ferguson, of the London Imperial College, bankrolled by Bill Gates, made a prediction early in 2020: by that summer, there would 500,000 COVID deaths in the UK, and 2 million in the US.

It was this absurd prediction, swallowed whole by Boris Johnson, and swallowed whole by Donald Trump, on the urging of Tony Fauci, that led to the original mass lockdowns in US and the UK. And then other nations followed suit.

As my long-time readers know, all this is just the tip of a very large iceberg. For the past year, I’ve been proving the SARS-CoV-2 virus doesn’t exist, the tests and case numbers are meaningless, and the highly destructive vaccine is unnecessary.

But I make frequent forays into the fantasy world of official science, to illustrate that, even within that lunatic bubble, internal contradictions and outright lies abound.

Here is my original 2020 article on the most famous and celebrated modeler in the world, Neil Ferguson [this is level three]:

—Neil Ferguson: the ghost in the machine—

Why do governments salute when he predicts a pandemic and tells them to lock down their countries?

Does anyone care about his past?

Why does he still have a prestigious job?

Who is he connected to?

Neil Ferguson, through his institute at London’s Imperial College, can call the shots on a major percentage of the global population.

He’s Mr. Genius, when it comes to projecting computer models of epidemics.

Fellow experts puff up his reputation.

According to the Business Insider (4/25/20), “Ferguson’s team warned Boris Johnson that the quest for ‘herd immunity’ [letting people live their lives out in the open in the UK] could cost 510,000 lives, prompting an abrupt U-turn [massive national lockdown in the UK]…His simulations have been influential in other countries as well, cited by authorities in the US, Germany, and France.”

Not only cited, not only influential, but swallowed whole.

Business insider continues: “On March 23 [2020], the UK scrapped ‘herd immunity’ in favor of a suppression strategy, and the country made preparations for weeks of lockdown. Ferguson’s study was responsible.”

There’s more. A lot more.

Same BI article: “Dr. Deborah Birx, coronavirus response coordinator to the Trump administration, told journalists at a March 16 press briefing that the Imperial paper [Ferguson’s computer projection] prompted the CDC’s new advice to work from home and avoid gatherings of 10 or more.”

Ferguson, instigator of LOCKDOWNS. Stripping away of basic liberties. Economic devastation.

So let’s look at Ferguson’s funding and track record, spelled out in the Business Insider piece:

“Ferguson co-founded the MRC Centre for Global Infectious Disease Analysis, based at Imperial, in 2008. It is the leading body advising national governments on pathogen outbreaks.”

“It gets tens of millions of dollars in annual funding from the Bill & Melinda Gates Foundation, and works with the UK National Health Service, the US Centres for Disease Prevention and Control (CDC), and is tasked with supplying the World Health Organization with ‘rapid analysis of urgent infectious disease problems’.”

Getting the picture?

Gates money goes to Ferguson.

Ferguson predicts dire threat from COVID, necessitating lockdowns—thus preparing people to accept a vaccine. The vaccine Gates wants.

Ferguson supplies a frightening computer projection of COVID deaths—to the CDC and WHO. Ferguson thus communicates a rationale for the Gates vaccine plan.

National governments surrender to WHO and CDC and order LOCKDOWNS.

Business Insider: “Michael Thrusfield, a professor of veterinary epidemiology at Edinburgh University, told the paper he had ‘déjà vu’ after reading the [Ferguson] Imperial paper [on COVID], saying Ferguson was responsible for excessive animal culling during the 2001 Foot and Mouth [mad cow] outbreak.”

“Ferguson warned the government that 150,000 people could die. Six million animals were slaughtered as a precaution, costing the country billions in farming revenue. In the end, 200 people died.”

“Similarly, he [Ferguson] was accused of creating panic by overestimating the potential death toll during the 2005 Bird Flu outbreak. Ferguson estimated 200 million could die. The real number was in the low hundreds.” HELLO?

“In 2009, one of Ferguson’s models predicted 65,000 people could die from the Swine Flu outbreak in the UK — the final figure was below 500.”

So you have to ask yourself, why would anyone believe what Ferguson has been predicting in this COVID hustle?

Are his fellow experts that stupid?

Are presidents and prime ministers that stupid?

And the answer is: This is a monumental covert op; some people are that stupid; some are caught up in the op and are afraid to say the emperor has no clothes; some are aware of what is going on, and they want to destroy national economies and lead us into, yes, a new world order.

Gates knows he has his man: Ferguson. As the recipient of tens of millions of dollars a year from the Gates Foundation, Ferguson isn’t about to issue a model that states: COVID is nothing to worry about, let people live their lives and we’ll be all right. The chance of that happening is on a par with researchers admitting they never actually discovered a new virus as the cause of illness in 2019, in Wuhan.

In order to justify injecting every man, woman, and child in the world with synthetic genes, Gates needs A STORY ABOUT A DEADLY VIRUS THAT NECESSITATES SHUTTING DOWN AND IMPRISONING THE PLANET, ACHIEVING A CAPTIVE AUDIENCE.

He’s got the story, all dressed up in a computer model, composed by a man with a past record of abject and devastating failures.

Neil Ferguson is the ghost in the machine. The machine is the World Health Organization and the CDC. The man behind the ghost is Bill Gates.

—Those are the three layers of this story. Fraud, fraud, and fraud. But don’t worry. Tony Fauci will smooth out the wrinkles and assure us all that we’re on the right track. We just have to destroy the village in order to save it. Piece of cake.


SOURCES:

https://www.dshs.state.tx.us/coronavirus/variant-faqs.aspx

https://www.lung.org/blog/covid-19-delta-variant

https://www.businessinsider.com/neil-ferguson-transformed-uk-covid-response-oxford-challenge-imperial-model-2020-4


Exit From the Matrix

(To read about Jon’s mega-collection, Exit From The Matrix, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

The Omicron Deception; how long can they string out the mutation-stories?

by Jon Rappoport

December 1, 2021

(To join our email list, click here.)

Nothing mutates faster than a non-virus, except perhaps Tony Fauci’s pronouncements about the “pandemic.”

In early 2020, it all started with a “virus” no one had isolated. Meaning a phantom, a fake, a con, a non-entity. NO VIRUS TO THIS DAY.

Now we’ve had fake variants of the fakes. Delta; Omicron from Africa.

The Stupidity Index—how stupid a person has to be in order to believe the official COVID narrative—is expanding. The more variants, the dumber obedient people have to be, to go along with the show.

At some point, as the number of variants grows, even people who resemble sloths living their lives hanging upside down in trees, will wake up.

“What was that new mutation last week? And this one today? It really comes from Antarctica? And we have to stay indoors for another month? I just want to tailgate and sit in a stadium and scream and drink and watch football…”

Which has already been happening this fall. By the millions, people are pouring into packed venues every weekend to watch pro, college, and high school football. On November 27th, 104,000 sat unmasked, cheek to jowl, in Michigan Stadium as their beloved home team upset Ohio State—and at the end of the game at least 20,000 fans came out on the field to celebrate. The field and the stands formed one vast sea of humanity. Variant? What variant? Delta? Omicron? Are they college fraternities?

Vegas bookies may be getting ready to post an over/under number on the final total of CDC/WHO variants. I say it would be 5.

At 5, people will lose track. They’ll forget the previous variants. They’ll tend to ignore COVID news altogether.

The basic tactic since the beginning has been: invent new fantasies to explain prior fantasies. For example, “Vaccinated people can still catch COVID.” That’s a fantasy because there is no virus. Now comes, “The vaccinated people catching COVID are really being infected by a variant; Delta or Omicron; that’s why the vaccine has become ‘less effective’.”

If you’ve ever forced yourself to sit through one of the hundred or so virus-outbreak movies, you know that at some point the scientific story line loses its impact. You’re thinking, “Let’s get to the car chase and the stuff blowing up and the people shooting each other.”

That’s what the movie is really about.

The COVID hoax is really about lockdowns and destruction of economies and lives and vaccine injury and death and tyrannical takeover of ruined society.

I’ll give you another number. It really does exist. It’s the grand total, worldwide, of people who are either: coming out into the street protesting the COVID restrictions and mandates; or ignoring them altogether and breaking all the rules and going about their lives unvaccinated.

I don’t know what that number is, but when it’s reached, the sociopaths will retreat. The genie will be out of the bottle for good.

Yes, it’s a very big number. But when has freedom not had a price?

Apparently, many people believe the number doesn’t matter, because God is going to intercede and make things right. It’s hard for me to imagine He’ll come through if most people, on their own, are doing NOTHING.

In the Old Testament, He seems to be chronically irked on this very point.

Starting in 1986, it took me two years to uncover the con that was HIV. I thought I had reached the bottom of it, but there were a few miles to go. Later, in the 1990s, I realized the bottom was NOTHING. That’s right. This sometimes is the case in really long cons. You drill all the way down and you find an empty space where you thought something existed.

The bottom of the HIV con—as with SARS-CoV-2—is: the virus doesn’t exist.

In prior articles, I’ve spelled this out in great detail.

It’s stage magic. There is no woman in the box. When the magician saws off her legs, she’s not there. As far as flesh is concerned, he’s sawing through nothing.

The magician is selling the audience’s illusion back to the audience.

As various propagandists have pointed out, the bigger the lie the easier it is to make it stick.

That’s because people are only familiar with small or moderate-sized lies; and because the amount of Structure which would be overturned by the exposure of a huge lie is too threatening.

“You mean the FDA and the CDC and WHO are all going down? Disappearing into dust? But I feel comfortable with them. They’re my friends. I don’t want to see them disappear…”

I do. And tomorrow wouldn’t be too soon.

And if the so-called branch of medical science called virology vanished from the Earth, there would be champagne corks popping in my house.

But for the moment, I’d be satisfied if all vaccine mandates everywhere were wiped off the books—just to give us some breathing room.

That revolution IS within our grasp, if enough of us build toward the critical-mass number I just alluded to above. It would be quite something to see. A fabulous jolt of adrenaline for the human race; for the right reason, for once.

Leave the Omicron and the Delta fantasies for the sloths on the couch. One day, they’ll stir from their trance and stumble along to catch up with us.


For almost two years, I’ve been demonstrating that SARS-CoV-2 doesn’t exist.

Instead, elite planners have been selling A STORY ABOUT A VIRUS.

In covert intelligence operations, this would be called a cover story. It obscures true goals. It justifies ongoing and future crimes that would otherwise be nakedly exposed.

For example, in my 1988 book, AIDS INC., I showed how the cover story about HIV was used in Africa.

For a very long time, the true causes of illness and death in areas of Africa have been: hunger; protein-calorie malnutrition; starvation; contaminated water supplies; poverty; war; farm land stolen from the people; corporate pollution; toxic medicines and vaccines; toxic pesticides; overcrowding in cities; lack of basic sanitation.

Most if not all of these causes could have been eliminated. But local governments did not want healthy people. Sick and dying people were easier to control, and taking away their land was an easier proposition.

Colluding with and paying off local government leaders, transnational corporations and foreign governments set up shop in these African countries and used the healthier people to work on their giant commercial farms and in their factories.

But in 1984, suddenly, there was a new (cover) story broadcast and sold to the world: what was really decimating Africa was HIV. THIS explained all the illness and dying.

The true causes, listed above, were shoved into the background.

Those true crimes were hidden, were permitted to continue unabated.

Not only that, the HIV cover story paved the way for pharmaceutical companies to rack up profits by selling extremely toxic AIDS drugs (e.g., AZT) to Africa.

The HIV test, which turned out false positives like Niagara Falls, made these drugs seem necessary—as fake case numbers soared.

People dying from the toxic medical treatments were, of course, listed as AIDS deaths.

And, as it turned out, HIV had never been isolated. Therefore, there was no proof it existed, no reason to suppose it existed.

Like AIDS, COVID-19 is also an intelligence-agency type covert op.

The short-term goal is wrecking economies. The long-term goal is taking the population into a new world of technocratic control.

Selling this as necessary all comes back to THE VIRUS COVER STORY.

“We’re not forcing technocracy down the throats of the people. Certainly not. We’re simply doing what we must, because of the danger of the virus…because everyone is a virus-spreader…(because too many people want their freedom)…”

Always identify and return to the cover story. Walk around it. Look at it from all sides. Walk into it from one side and exit from the other. Test it. The vital clues are there.


Another classic example: 2009, La Gloria, Mexico. Smithfield Foods, the largest pork producer in the world, operates a giant pig farm. 950,000 pigs.

The poisonous urine and feces from these 950,000 pigs run out into the open air and form what are called lagoons. They’re so large, you can see them from outer space.

Workers spray the toxic lagoons with a toxic foam. It’s routine.

Workers, and people in the surrounding neighborhood, are getting sick and dying. So new contractors are brought in to spray the lagoons with yet another toxic chemical.

Out of nowhere, guess who shows up? The CDC.

Guess what they conclude? It’s not the urine and feces lagoons or the toxic chemicals causing illness and death. No. Of course not.

It’s a new mysterious “virus.” H1N1.

And voila, we have a new cover story and a new epidemic, called Swine Flu.

The cover story serves a number of purposes, as time passes. But the most obvious one is: Smithfield Foods is protected. They get away with murder.

And to cap it all off, four years later, in 2013, Smithfield, still protected, sells itself to a Chinese company, Shuanghui International Holdings, for $4.72 billion.


Here’s what I wrote about Zika (another phantom virus) in 2015:

“Medical CIA” provides the cover story.

In Brazil, the so-called center of the “Zika epidemic,” there are many problems in poverty-stricken areas that involve more than babies being born with small heads and brain impairment.

The grinding poverty itself, of course. Stolen farm land. Widespread corporate use of poisonous pesticides, some of which are banned in 22 other countries. Contaminated water supplies. Lack of basic sanitation. Overcrowding. Prior vaccine campaigns, in which toxic substances were injected directly into the bodies of people whose immune systems were already on the verge of collapsing. Toxic medical drugs.

In 2014, the Tdap vaccine (tetanus, diphtheria, whooping cough) was recommended for pregnant women. Among other toxic substances, this vaccine contains aluminum compounds. Aluminum can cross the blood-brain barrier and cause damage.

Workers are now fumigating areas with toxic sprays to kill mosquitoes. Soldiers are going door to door, handing out more toxic mosquito sprays for indoor use.

Combine all these factors, and you have an ongoing catastrophe.

It makes a great deal of sense to highlight, promote, and blame the “Zika virus” for what is actually going on in Brazil, if you want to distract and divert and obscure.

If you stopped the vaccine campaigns, stopped the spraying, and remedied the conditions I listed above, the health of the population would return and revive, without medical intervention.

Of course, the governments and their allied corporations have no intention of returning stolen land to the people. They have no intention of stopping the use of poisonous pesticides. Medical authorities have no intention of admitting they are concocting a story about a “virus,” Zika, as a cover for their corporate and government allies, and as a pretext to have “a new disease” to treat and work on and solve. They have no intention of stopping toxic vaccine campaigns.

To cap it all off, the conditions the “virus” is supposed to be causing—babies born with small heads and brain damage—can result from ANY injury or insult to a pregnant woman or her infant. No virus required.

But…“Look here, at the virus. Don’t look there.”

Cover story.


power outside the matrix

(To read about Jon’s collection, Power Outside The Matrix, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

Virus mutation in Jewish deli infecting all of Africa came from Beverly Hills

by Jon Rappoport

November 30, 2021

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Tony Fauci, the Great White Father, is flying to Africa, to save the continent from the latest virus-mutation, which originated in a deli in Beverly Hills.

Fauci gave a statement to reporters at LAX before departing: “We now know that what we’re calling SARS-CoV-6 crossed species from a pastrami sandwich at Fineberg’s Deli on Rodeo Drive, to Fred Reilly, a customer, in late October. Reilly flew to Botswana, where he infected three soccer players who were moonlighting as security guards at a UN cocktail party.”

Fauci will explain to Africa that a new IG Farben drug, RP-1984, which has been stockpiled for 20 years, since it failed to slow the progression of leukemia in rats, will be dropped from planes over the continent.

The drug attacks all cells of the body, preventing them from replicating. The hope is it will also prevent the deli variant from replicating before it kills the host (human beings).

“Preliminary data looks promising,” Fauci stated. “Of course, lockdowns for at least a year, vaccination, mask wearing, and distancing will have to be practiced religiously,” he added.

“Owing to business closures, most African countries will sink into irreversible and desperate debt. The International Monetary Fund, as usual, will tide these countries over with loans. However, this time, the United Nations will usher in a new digital currency for Africa.”

The currency, Fauci asserted, will include Universal Guaranteed Income for every person in Africa—as long as they obey all government dictates without question or protest.

At the White House, Joe Biden said, “I don’t eat pastrami. Nurse Jill won’t let me.”

Deli owner Hank Fineberg told the LA Times, “We didn’t start this. We buy our pastrami from Gornish Garnish, a wholesaler in Brooklyn. Why isn’t the CDC investigating them? Besides, none of our customers have actually gotten sick. So what’s the problem?”

The Times attributes the plunge of the stock market to the deli variant. It also questions California Governor Gavin Newsom’s decision to “leave Rodeo Drive open to shoppers.”

Bill Gates is urging people to eat a pastrami substitute made from dried maple leaves, a pine tar derivative, and salted mica.

A new study published in the New England Journal of Medicine concludes that “the deli variant causes the body to produce 12 different sets of antibodies, some of which resemble the original SARS-CoV-2. The body then faces the prospect of antibodies attacking antibodies, resulting in a downward vortex resembling a black hole in space…”

NBC states, “Black Lives Matter leaders are huddling with officials at the Ford Foundation, shaping a response to news that the deli variant is sweeping through Africa.”

CBS: “In Africa, the major symptoms associated with the deli variant are weight loss, dehydration, and diarrhea. These symptoms traditionally stem from malnutrition and starvation, but researchers say the variant is now the principal culprit…”

At the White House yesterday, the President’s Press Secretary, Jen Psaki, told reporters, “The dark winter has arrived early. It’s here. The deli variant will necessitate new lockdowns and business closures. President Biden will be issuing a new wide-ranging vaccine mandate in the next few days. At the moment, he is meeting with NIH researchers and poring over the latest data on infection rates. His background in statistical analysis will serve him well in this effort…”

A FOX News reporter asked, “Will Christmas be canceled?”

Psaki replied, “Shopping will proceed. But Jesus was born only once. Is it necessary to keep celebrating the event? The Secretary of State is meeting with Pope Francis to discuss the question.”

The FOX reporter followed up with another query: “What about all the migrants coming across the Southern border? How many are carrying the deli variant?”

Psaki: “We have a new mass testing program called The Wand. It can survey thousands of people at once and detect the presence of viruses. So far, we’ve found only one person at the border who is infected with the deli variant—a former Montana resident. He has been the subject of an FBI manhunt, owing to the fact that he was present at the January 6th Capitol breach. He is now in custody at Walter Reed Hospital. He has no symptoms, which is a bit of a mystery.”

Retiring NIH Director Francis Collins clarified several deli variant issues this morning, on a conference call with reporters: “The new variant is producing different effects in different populations. In Africa, we’re seeing weight loss, dehydration, and diarrhea. In South America, the primary symptom is a dry cough. In Australia, it’s transient leg pain and anger. In Europe, numbness of the extremities and increasing poverty. In the US, waning immunity conferred by the vaccine, hypnotic passivity, and paradoxically, attendance at football games…”

Senator Chuck Schumer has introduced a bill that will compensate victims of the deli variant, in the form of a federal card that can be used to purchase $900 in goods and services. The diagnosing doctor will also receive a card, worth $3900 for each variant case identified.

Don’t leave home without it. Actually, don’t leave home. Lock down.


Exit From the Matrix

(To read about Jon’s mega-collection, Exit From The Matrix, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

The new African virus mutation: right on time; a kindergarten covert op for the ignorant

by Jon Rappoport

November 29, 2021

(To join our email list, click here.)

There are no variants.

Because there is no virus. SARS-CoV-2 doesn’t exist. I’ve spent the past year and a half proving that. [0]

But fantasies do exist. So do covert ops with intentions to deceive.

Thus, the “scientific world” is agog over the new South African variant, named B11529 (aka Omicron, Botswana). Woo. The ghost is coming out of the closet. Beware. COVID cases are rising…

“We don’t know whether the vaccine will be effective in the face of the new variant. New lockdowns may be necessary. Travel restrictions are coming. Batten down the hatches.”

I mean, really.

As you know, for the past few months stories in the press have been claiming the vaccine-conferred immunity is sinking like a stone. This story is absurd because, again, there is no virus. So there was no conferred immunity to begin with. But anyway, that’s the story that’s been circulating. So NOW…

“It turns out one major reason for the diminished effectiveness of the vaccine is…

“The NEW VARIANT. The South African B11529.”

Uh-huh. “The vaccine is having a tough time preventing infection caused by the new variant. We may need to enforce boosters every three months…”

Keep the fear going. Push harder for the vaccine. Explain away its failures. Fabricate rising case numbers, blaming them on the new variant. Institute heavy new lockdowns.

“The South African variant is deadlier than the Delta, which is deadlier than the original.”

And none of the three exists.

What does exist is fantasy, piled higher and deeper and thicker.

The variant is Fauci. The variant is Bill Gates. The variant is CDC/WHO. The variant is the World Economic Forum. And the Chinese regime. And presidents and governors. And the mainstream press.

And don’t forget this. Vaccine injuries and deaths have been escalating all over the world. In the US alone, reported injuries have broken above 600,000 [1]. As I’ve mentioned, the well-known Harvard Pilgrim Healthcare study [2] concluded that, to obtain a true number of injuries, multiply the reported figure by 100.

Something is needed to explain all these injuries and deaths. That is, to lie about them.

And right on time, here comes the new variant.

“These people who seem to be injured by the vaccine are really keeling over from the original virus, the Delta, and woo, the South African B11529.”

Also: Recently, we’ve seen a spate of press stories with the theme—“scientists are mystified by the low COVID case numbers in Africa, where the vaccination rates are very low.” [3] Boom. That story is now gone. Wiped out. Now it’s THE WORLD IS BEING ATTACKED BY THE SOUTH AFRICAN B111529 VARIANT.


Here is one of my articles covering the non-existence of SARS-CoV-2:

—Dr. Andrew Kaufman refutes “isolation” of SARS-Cov-2; he does step-by-step analysis of a typical claim of isolation; there is no proof that the virus exists—

The global medical community has been asserting that “a pandemic is being caused by a virus, SARS-Cov-2.”

But what if the virus doesn’t exist?

People have been asking me for a step-by-step analysis of a mainstream claim of virus-isolation. Well, here it is.

“Isolation” should mean the virus has been separated out from all surrounding material, so researchers can say, “Look, we have it. It exists.”

I took a typical passage from a published study, a “methods” section, in which researchers describe how they “isolated the virus.” I sent it to Dr. Andrew Kaufman [4], and he provided his analysis in detail.

I found several studies that used very similar language in explaining how “SARS-CoV-2 was isolated.” For example, “Severe Acute Respiratory Syndrome Coronavirus 2 from Patient with Coronavirus Disease, United States, (Emerging Infectious Diseases, Vol. 26, No. 6 — June 2020)” [5].

First, I want to provide a bit of background that will help the reader understand what is going on in the study.

The researchers are creating a soup in the lab. This soup contains a number of compounds. The researchers assume, without evidence, that “the virus” is in this soup. At no time do they separate the purported virus from the surrounding material in the soup. Isolation of the virus is not occurring.

They set about showing that the monkey (and/or human cells) they put in the soup are dying. This cell-death, they claim, is being caused by “the virus.” However, as you’ll see, Dr. Kaufman dismantles this claim.

There is no reason to infer that SARS-CoV-2 is in the soup at all, or that it is killing cells.

Finally, the researchers assert, with no proof or rational explanation, that they were able to discover the genetic sequence of “the virus.”

Here are the study’s statements claiming isolation, alternated with Dr. Kaufman’s analysis:

STUDY: “We used Vero CCL-81 cells for isolation and initial passage [in the soup in the lab]…”

KAUFMAN: “Vero cells are foreign cells from the kidneys of monkeys and a source of contamination. Virus particles should be purified directly from clinical samples in order to prove the virus actually exists. Isolation means separation from everything else. So how can you separate/isolate a virus when you add it to something else?”

STUDY: “…We cultured Vero E6, Vero CCL-81, HUH 7.0, 293T, A549, and EFKB3 cells in Dulbecco minimal essential medium (DMEM) supplemented with heat-inactivated fetal bovine serum (5% or 10%)…”

KAUFMAN: “Why use minimal essential media, which provides incomplete nutrition [to the cells]? Fetal bovine serum is a source of foreign genetic material and extracellular vesicles, which are indistinguishable from viruses.”

STUDY: “…We used both NP and OP swab specimens for virus isolation. For isolation, limiting dilution, and passage 1 of the virus, we pipetted 50 μL of serum-free DMEM into columns 2–12 of a 96-well tissue culture plate, then pipetted 100 μL of clinical specimens into column 1 and serially diluted 2-fold across the plate…”

KAUFMAN: “Once again, misuse of the word isolation.”

STUDY: “…We then trypsinized and resuspended Vero cells in DMEM containing 10% fetal bovine serum, 2× penicillin/streptomycin, 2× antibiotics/antimycotics, and 2× amphotericin B at a concentration of 2.5 × 105 cells/mL…”

KAUFMAN: “Trypsin is a pancreatic enzyme that digests proteins. Wouldn’t that cause damage to the cells and particles in the culture which have proteins on their surfaces, including the so called spike protein?”

KAUFMAN: “Why are antibiotics added? Sterile technique is used for the culture. Bacteria may be easily filtered out of the clinical sample by commercially available filters (GIBCO) [6]. Finally, bacteria may be easily seen under the microscope and would be readily identified if they were contaminating the sample. The specific antibiotics used, streptomycin and amphotericin (aka ‘ampho-terrible’), are toxic to the kidneys and we are using kidney cells in this experiment! Also note they are used at ‘2X’ concentration, which appears to be twice the normal amount. These will certainly cause damage to the Vero cells.”

STUDY: “…We added [not isolated] 100 μL of cell suspension directly to the clinical specimen dilutions and mixed gently by pipetting. We then grew the inoculated cultures in a humidified 37°C incubator in an atmosphere of 5% CO2 and observed for cytopathic effects (CPEs) daily. We used standard plaque assays for SARS-CoV-2, which were based on SARS-CoV and Middle East respiratory syndrome coronavirus (MERS-CoV) protocols…”

STUDY: “When CPEs were observed, we scraped cell monolayers with the back of a pipette tip…”

KAUFMAN: “There was no negative control experiment described. Control experiments are required for a valid interpretation of the results. Without that, how can we know if it was the toxic soup of antibiotics, minimal nutrition, and dying tissue from a sick person which caused the cellular damage or a phantom virus? A proper control would consist of the same exact experiment except that the clinical specimen should come from a person with illness unrelated to covid, such as cancer, since that would not contain a virus.”

STUDY: “…We used 50 μL of viral lysate for total nucleic acid extraction for confirmatory testing and sequencing. We also used 50 μL of virus lysate to inoculate a well of a 90% confluent 24-well plate.”

KAUFMAN: “How do you confirm something that was never previously shown to exist? What did you compare the genetic sequences to? How do you know the origin of the genetic material since it came from a cell culture containing material from humans and all their microflora, fetal cows, and monkeys?”

—end of study quotes and Kaufman analysis—

My comments: Dr. Kaufman does several things here. He shows that isolation, in any meaningful sense of the word “isolation,” is not occurring.

Dr. Kaufman also shows that the researchers want to use damage to the cells and cell-death as proof that “the virus” is in the soup they are creating. In other words, the researchers are assuming that if the cells are dying, it must be the virus that is doing the killing. But Dr. Kaufman shows there are obvious other reasons for cell damage and death that have nothing to do with a virus. Therefore, no proof exists that “the virus” is in the soup or exists at all.

And finally, Dr. Kaufman explains that the claim of genetic sequencing of “the virus” is absurd, because there is no proof that the virus is present. How do you sequence something when you haven’t shown it exists?

Readers who are unfamiliar with my work (over 300 articles on the subject of the “pandemic” during the past year [7]) will ask: Then why are people dying? What about the huge number of cases and deaths? I have answered these and other questions in great detail. The subject of this article is: have researchers proved SARS-CoV-2 exists?

The answer is no.

—end of Kaufman article—


And while I’m at it, here is another piece I wrote last year about how virus-propaganda (fairy tales) must be managed, in order to make the masses stand up and salute:

—The “hot zone” theory of new frightening diseases—

Remember? There was a 1994 book by that name— and then “experts” began piling on—it went something like this:

“Out of the deep dark rainforests of Earth (cue sounds of native drumming), as a result of modern plane travel, viruses we’ve never encountered before will spread epidemics across the globe. Our immune systems, ill-equipped to recognize or deal with these strange killer germs, will fold up under the pressure, and all of civilization will be threatened with extinction.”

Let’s see. Since planes fly back and forth, and since all sorts of Westerners travel TO the rainforests, why haven’t we seen whole native tribes wiped out by viruses from the deep dark streets of Brooklyn?

It would even seem that viruses, common in, say, Norway, would cause trouble in Oregon.

Why does it have to be “viruses from jungles?” Or other faraway places like China? Why can’t we have the Second City Virus, emanating from a slaughterhouse in Chicago and infecting people in Nigeria? Why can’t we have a Big Easy virus from New Orleans traveling to Beijing?

Is it possible that jungles and Africa and China and Mexico are typically chosen for virus fairy tales because, in the minds of many Westerners, they satisfy a requirement of “strange,” “different,” “primitive,” and so on? We’re talking theater here—and when you stage a propaganda play (fiction), you want to tap into the reflex instincts of the audience. The Hartford Virus, the Des Moines Virus, the Vancouver Virus just don’t fit the bill.

Because they can’t drive up the fear that jungles or Africa or China can.

Unless you’ve been living in an ice cave in the Arctic, you know selling fear of THE VIRUS is big business. To do that, you have to strike the right notes.

I personally would be interested in a Beverly Hills or a Scarsdale or a Park Avenue epidemic virus story. I’d like to see the media try to sell that one.

What about a Bill Gates Seattle virus that some Patient Zero unknowingly carries on a plane flight to Mexico City?

Think it through. We NEVER hear killer virus stories about germs traveling from Europe and America to Asia and Africa. Why not? Because such a story won’t sell. It won’t bite.

This is called a clue.

It tells you that virus-stories are shaped and managed and written and managed and broadcast according to a plan that has nothing to do with actual disease.

If a monkey in Africa can bite a man and thus transmit a virus to the West, then a salesman in Duluth can sneeze on a man at a local airport and thus send a virus to Ethiopia.

But amazingly, through secret communication among viruses, it never happens that way. The germs have decided what the traffic pattern is, and the CDC and the World Health Organization are just discovering What Is.

Sure they are. And if you buy that, I have condos for sale on the far side of the moon.


SOURCES:

[0] https://blog.nomorefakenews.com/tag/virus/

[1] https://rickjaffeesq.com/2021/02/19/what-the-heck-is-the-harvard-pilgrim-study-and-did-it-really-say-that-about-the-underreporting-of-vaccine-adverse-events/

[2] https://openvaers.com/covid-data

[3] https://apnews.com/article/coronavirus-pandemic-science-health-pandemics-united-nations-fcf28a83c9352a67e50aa2172eb01a2f

[4] https://andrewkaufmanmd.com/

[5] https://wwwnc.cdc.gov/eid/article/26/6/20-0516_article

[6] https://www.thermofisher.com/us/en/home.html

[7] https://blog.nomorefakenews.com/category/covid/


The Matrix Revealed

(To read about Jon’s mega-collection, The Matrix Revealed, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

COVID concentration camps for Australians; it’s happening

by Jon Rappoport

November 24, 2021

(To join our email list, click here.)

Zero Hedge, November 22, 2021: “The Australian army has begun forcibly removing residents in the Northern Territories to the Howard Springs quarantine camp located in Darwin, after nine new Covid-19 cases were identified in the community of Binjari. The move comes after hard lockdowns were instituted in the communities of both Binjari and nearby Rockhole on Saturday night.”

“’Residents of Binjari and Rockhole no longer have the five reasons to leave their homes,’ said Northern Territory chief minister, Michael Gunner, referring to the country’s five allowable reasons to avoid lockdown (buying food and supplies, exercising for up to two hours, care or caregiving, work or education if it can’t be done from home, and to get vaccinated at the nearest possible location).”

“’They can only leave [home] for medical treatment, in an emergency, or as required by law’.”

“’It’s highly likely that more residents will be transferred to Howard Springs today, either as positive cases or close contacts,’ he continued, adding ‘We have already identified 38 close contacts from Binjari but that number will go up. Those 38 are being transferred now’.”

“’I contacted the Prime Minister last night. We are grateful for the support of about 20 ADF personnel, as well as army trucks to assist with the transfer of positive cases and close contacts – and to support the communities’.”

“’We are doing an assessment today of what extra resources we might need from the Feds, and the Prime Minister is ready to help further – I thank him for that’.”

“Five days ago, NT [Northern Territories] Senator Malarndirri McCarthy told ABC that over crowding in Indigenous communities was a ‘massive problem,’ pointing to the region’s second cluster of new infections – which included nine members of McCarthy’s direct family, including her sister who flew from Katherine to Robinson River while unknowingly bringing COVID-19 with her, per the report.”

The sociopaths and their stormtroopers who run Australia would make Hitler and Stalin envious. “You mean you can exercise iron control over a whole nation based on a STORY ABOUT A VIRUS?”

I’ve received a report from Australia showing numbers of protesters against the national vaccine mandate, in key cities, for the weekend of November 20-21. The total is close to a million people—in a nation of 25 million. That’s stunning.

Hopefully, those numbers will increase.

Update: another report from Australia; the military have begun forcing vaccinations on the aborigines in the Northern Territory.

It’s abundantly clear we’re not living in the same world we were two years ago. That world doesn’t exist anymore.

Watch this shocking video made by June Mills, an aboriginal elder in the Northern Territory. As she excoriates the fascist Chief Minister of the Territory, Michael Gunner, and calls on her people in other towns to report on what’s happening to them and what the Army is doing, ask yourself: Is this the irrational raving of a woman who’s gone over the edge, or is this exactly how a sane person would react when government killers are loose in her neighborhood?


SOURCES:

https://www.zerohedge.com/covid-19/australian-army-begins-transferring-covid-positive-cases-contacts-quarantine-camps

https://www.facebook.com/TerritoryChief/posts/435285761296933 (Micheal Gunner’s statement)

https://aecom.com/projects/manigurr-ma-village/ (Howard Springs COVID concentration camp)

https://www.brighteon.com/cf5650c2-4167-4be8-9ca6-47d2bb52961d (June Mills’s call to action)


The Matrix Revealed

(To read about Jon’s mega-collection, The Matrix Revealed, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

A pandemic of the vaccinated

And to keep the REAL pandemic going, we must have vaccine mandates and passports and crackdowns on the unvaccinated

by Jon Rappoport

November 23, 2021

(To join our email list, click here.)

Daily Mail, November 18, 2021: “Dr. Anthony Fauci, the director of the National Institute for Allergy and Infectious Diseases, said waning immunity from the initial shots is leading to a rise in severe cases among immunized Americans. ‘What we’re starting to see now is an uptick in hospitalizations among people who’ve been vaccinated but not boosted’…”

NY Times podcast, November 12, 2021; Fauci states: “They are seeing a waning of [vaccine-induced] immunity not only against infection but against hospitalization and to some extent death, which is starting to now involve all age groups. It isn’t just the elderly.”

Translation: The vaccine is severely injuring and killing MANY people, but of course we’re calling those injuries and deaths “COVID-19 disease.” Also, our solution to this catastrophe is piling on MORE injections (boosters), which will hospitalize and kill even MORE people.

The dailyexpose.uk has the much deeper story:

“The public are being repeatedly lied to by elected officials, unelected advisors, and the mainstream media, with all of them claiming that the world is currently experiencing a Pandemic of the Unvaccinated. This could not be further from the truth.”

“But the lie has now been used to justify locking down the unvaccinated in Austria, and locking the unvaccinated out of society in Australia.”

“Now Germany is about to follow suit, Scotland is about to ban the unvaccinated from pubs and restaurants under the advice of a qualified nutritionist posing as a Pandemic expert who goes by the name of Devi Sridhar, and the authorities and media in England have gone into overdrive on the advice of the ‘nudge unit’ to sway the population into supporting a lockdown for only the unvaccinated.”

“But it all makes absolutely no sense because official Public Health data shows that over the past three months… two-thirds of Covid-19 hospitalisations [people who get very sick from the shot] have been among the fully vaccinated, and a frightening 91% of Covid-19 deaths [people who die from the shot] have been among the fully vaccinated, and projections shows things are about to get a lot worse.”

“…in the week beginning November 6th a total of 773 Covid-19 hospitalisations [people injured by the shot] were confirmed in Scotland. Of these 137 were among the unvaccinated population, whilst 363 were among the vaccinated population.”

“…the fully vaccinated accounted for the majority of hospitalisations [in Scotland] between October 16th and November 12th, and again by taking into account hospitalisations as far back as August 23rd we can see that things have been getting progressively worse for the fully vaccinated by the week.”

“In the week beginning August 21st the vaccinated accounted for 68% of hospitalisations, but fast forward to the week beginning November 6th and we can see that the vaccinated accounted for 73% of hospitalisations.”

“The worst week so far for the vaccinated however, in terms of hospitalisations, came in the week beginning October 16th which saw the vaccinated population account for 79% of Covid-19 hospitalisations [people injured by the shot].”

“[In Scotland]…the fully vaccinated accounted for the overwhelming majority of Covid-19 deaths [deaths from the shot] between October 9th and November 5th 2021. But by also taking into account the number of…deaths by vaccination status as far back as August 14th we’re able to see that things are getting significantly worse for the fully vaccinated population by the week…”

“…the week beginning August 14th the vaccinated accounted for 78% of deaths, but fast forward to the week beginning October 30th and we can see that the vaccinated accounted for 85% of deaths.”

Switching from Scotland to England: “The latest Public Health England technical briefing on Covid-19 variants of concern has been published and it reveals that up to the 12th September 2021, 74% of all alleged Covid-19 deaths since August 2nd 2021 [people killed by the shot] have been among the vaccinated population, confirming the UK is currently experiencing a pandemic of the vaccinated.”

But don’t worry, be happy. The solution—endless toxic boosters—will surely save the day. And by “save the day,” I mean tens or even hundreds of millions of lives will be ruined and ended.

And by “save the day,” I also mean the news media will cover all this up and continue to promote an alternative fantasy of a universe, in which the vaccine is a rescuing rainbow and the unvaccinated are terrorists.

There’s magic at work here. If you believe what the news media are telling you, then you’ll remain vibrant and healthy (if you take the vaccine and all the boosters). If you don’t take the vaccine, you’re doomed. It’s really quite something. Those talking news heads are elves from the forest. With every word they utter, they cast powerful spells.

That’s why the really smart people trust the news and embrace the elves.


SOURCES:

https://www.dailymail.co.uk/health/article-10217977/Fauci-says-Covid-hospitalizations-rising-fully-vaccinated-people.html

nytimes.com/2021/11/12/podcasts/the-daily/anthony-fauci-vaccine-mandates-booster-shots.html?showTranscript=1

https://dailyexpose.uk/2021/11/18/91-percent-covid-19-deaths-among-the-fully-vaccinated/


The Matrix Revealed

(To read about Jon’s mega-collection, The Matrix Revealed, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

COVID vaccine: missing key

Where’s the wiggle?

by Jon Rappoport

November 18, 2021

(To join our email list, click here.)

—In the US alone, reported COVID vaccine injuries have topped 600,000. The well-known Harvard Pilgrim study concludes you should multiply the number of reported vaccine injuries by 100 to arrive at a true number—

In any field where information is vital, the omissions are often worse than the lies.

In this article, I point out one such glaring omission, when it comes to the safety of COVID vaccines.

Tracking vaccine injuries and deaths through reports to databases is one avenue; another avenue would be direct studies of people who have been vaccinated.

Proper studies have not been done. Omission.

This would be a proper study: For starters, based on what MANY clinicians are seeing, develop/confirm true markers for: blood clots, including micro-clots; specific heart dysfunctions; miscarriages; menstrual cycle disruption; infertility; toxic effects on cells (e.g., the presence of graphene oxide); the appearance of the spike protein in cells, in areas of the body where the protein should not appear.

Enroll, in a modest pilot study, 1000 people who have received one of the RNA COVID vaccines. Run tests on these people (blood, tissue, pictures) looking for these markers.

I’m NOT talking about a few photos of one patient’s blood. I’m talking about a full study of 1000 people, for starters.

You would think such a study has already been done, because only sheer ignoramuses or criminals would fail to realize that, when you inject people with substances, you should discover the effects BY STUDYING THE EFFECTS.

Somebody suffers a blow to the head, you take a picture of the head and look at the effects. Somebody injects a person with liquid containing 10 ingredients, you run tests to find out what negative consequences may have occurred.

Unfortunately, most people are so hypnotized by the IDEA of medical science, they assume that if a study hasn’t been done, it doesn’t need to be done.

Lab workers all over the world will torture test animals, by injecting them with larger and larger doses of a compound in a new cosmetic, to discover the dose that kills the animals. But doing harmless tests on people who have received a new vaccine is out of the question.

To gain insight on the scientists who refuse to run the tests I’m proposing on vaccinated people, these are the same scientists who say, “Yes, a number of people died after vaccination, but there is no evidence the injection caused those deaths.”

What they mean is, “We didn’t look to see whether the vaccine caused the deaths, and furthermore, we don’t know how to establish causation. We’ve never worked that out.”

Which is like saying, “The chemical that entered the river from a pipe in the factory? We haven’t done sufficient studies on the chemical to determine whether it causes cancer. Therefore, the 96 plaintiffs with cancer who are suing the company have no case. Causation cannot be proved. It will never be proved, because we will never study the chemical.”

There is another factor at work. Many people who are interested in scandals are only interested in the details of overt crimes. “They shot him and buried his body in a landfill? Are there pictures of the decaying corpse? The killer was married to the victim’s sister? Was she in on it?”

“Clinton and Monica in a little room off the Oval Office? Did you see the photo of the stained dress?”

If you tell these people the biggest scandal in a situation is OMISSION— what DIDN’T HAPPEN, WHAT SHOULD HAVE BEEN DONE, BUT WASN’T—they fade out and walk away.

Ask these people the following question: Which would you prefer? LOOKING at one microscope photo of one drop of blood from one vaccinated person that might show a wiggling line that might be a live organism? Or KNOWING that the absolutely essential safety study of a vaccine that has been injected into 3.6 billion people has never been done?

“Let me see the picture. I want to see the photo. Where’s the wiggle?”

This article is for the people who give the other answer.

And for scientists who know that mass maiming and killing also involve a crime of omission.

“We know the vaccines are safe because we didn’t study the people who got the vaccine.”


power outside the matrix

(To read about Jon’s collection, Power Outside The Matrix, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

Fifteen million Jews, the vaccine, and the conscience to refuse

by Jon Rappoport

November 17, 2021

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In the US alone, reported vaccine injuries have soared past 600,000.

The well-known Harvard Pilgrim Healthcare study concluded that, in order to obtain a true number for such injuries, you would need to multiply the reported figure by 100.

First, it was two shots. But then the format was changed. There would be a booster. Then, not just one booster, but at least two. And for months, experts have suggested that the program will evolve into yearly shots.

On top of that, proof of vaccination is now demanded. The passports. The government, of course, controls these passports, which allow vaccinated persons to participate in ordinary social life. Those without passports are confined, restricted, in a form of slavery. And the passport will be revoked if a person doesn’t line up for all required boosters.

In other words, this has been a step-operation, with the individual’s rights constrained and eaten into, progressively, over time—finally resulting in his complete capture by the State.

And so I refer you to the story of Joseph in the Old Testament. The real story. It holds a valuable lesson.

As you recall, Joseph was the favored son of Jacob. Joseph’s jealous brothers sold him into slavery. While imprisoned in Egypt, Joseph revealed his ability to interpret dreams.

He was eventually brought before the Pharaoh, who needed someone who could tell him what his troubling dream meant: seven starving cows ate seven well-fed cows; seven dead ears of corn ate seven plump ears.

Joseph told the Pharaoh there would be seven years of plenty in the land, and then seven years of famine. Therefore, the Pharaoh should immediately store up grain.

When the terrible famine hit, Joseph, who was now the Pharaoh’s vizier, dealt with the MANY hungry people who came to buy bread. In exchange for the bread, Joseph first demanded that the people sell their possessions to the State; then, their property; and finally themselves. AS SLAVES. A step-operation.

When next we learn of the condition of the Jews in Egypt, in the story of Moses, the Jews are slaves. Do you suppose this turnabout had something to do with Joseph’s “solution” to the famine and the anger it raised in the population?

Of course, the Bible story focuses on Joseph reuniting with his brothers and his father, all of whom who believed he died.

The story passes no judgment on Joseph, who put a population into slavery to the State.

Those of the Jewish faith must consider this tale from Genesis, because it is parallel to what is happening now: a Globalist elite is bent on capturing the population degree by degree, with its “solution.”

In Genesis, after the famine was over, the Egyptians, who continued to farm grain, were planting government seeds on government land, and they had to turn over a fifth of their crop to the Pharaoh. There was no privately owned land.

If that doesn’t ring any bells, what will?

Jews today are being betrayed by their leadership, who are aligned with the State. Jews are being told “the best medical minds” have decided the vaccine is safe and effective and only wild conspiracy theorists believe otherwise.

So as usual, it falls to the conscience and common sense of the individual to ignore the official word.

The lying, criminal, murderous official word.

It falls to the conscience of Jewish parents to protect their children against the shot, no matter what. And to protest against the mandates and the passports.

How long did Moses and his people wander in the desert? 40 years? Given that extreme ordeal, can modern Jews work up the courage to say no to a destructive vaccine and an enslaving mandate?

Or do modern Jews actually believe God wants them to take the shot?

Because unless I’m mistaken, the religion of the Jews is centered on the One God. That is its whole point. That was its whole point, when Jews declared, not many gods, only one.

Of course, DOCTORS are quite adept at playing God. So perhaps the leadership councils of the Jewish faith should come out and switch their allegiance. WE NOW PRAY TO DOCTORS. WE NOW MUST HAVE THE PERMISSION OF DOCTORS. WE MUST HAVE NO IDOLS THAT SUPERSEDE DOCTORS.

“Sh’ma Yisrael Adonai Eloheinu Adonai Eḥad.” “Hear O Israel, the doctor our doctor, the doctor is one.” Say it. Bow the head and bend the knee and say it. The new prayer.

Or find your soul and your conscience and your God and throw off the chains of your slavery.

If you’re a Conservative Jew or a Reform Jew, you’re going to have to wake up from the chapter you and your rabbis added to the Old Testament. It’s called SUBURBAN LIFE. It mainly involves new temples designed by talentless architectural morons and the eternal building funds maintained to pay for those temples. I know; I was steeped in that neighborhood “culture” as a child. Fortunately, my parents had moral spine, but that’s a different story for a different time.

To you 15 million Jews: there are two swords. One is wielded by the doctors. The other is wielded by your God. Make your decision and your choice.


Exit From the Matrix

(To read about Jon’s mega-collection, Exit From The Matrix, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.