A paper published on October 1, 2022, entitled: “A Case Report: Multifocal Necrotizing Encephalitis and Myocarditis after BNT162b2 mRNA Vaccination against COVID-19,” by Michael Mörz in the journal Vaccines, details how a 76-year old man who died received an autopsy. The man who was thought not to have been ill from covid, was found to have necrotising, that is tissue-death effects of both brain and heart tissue, and mRNA spike proteins were found in both areas. The article notes that there have been other reports of these effects. As Steve Kirsch summarises, “the vaccines can kill cells in your brain and your heart causing you to die.” Many people must now be the biological equivalents of ticking time bombs.

https://stevekirsch.substack.com/p/it-is-now-known-that-the-covid-vaccines

“A new paper in the peer-reviewed medical literature just came out showing the COVID vaccines, and not COVID, is causing myocarditis and encephalitis leading to death.

The paper is entitled: A Case Report: Multifocal Necrotizing Encephalitis and Myocarditis after BNT162b2 mRNA Vaccination against COVID-19.

It was published yesterday, Oct 1, and now has already has over 100,000 views of the abstract and over 6,000 views of the full text.

Here’s the abstract (highlights are mine):

The current report presents the case of a 76-year-old man with Parkinson’s disease (PD) who died three weeks after receiving his third COVID-19 vaccination. The patient was first vaccinated in May 2021 with the ChAdOx1 nCov-19 vector vaccine, followed by two doses of the BNT162b2 mRNA vaccine in July and December 2021. The family of the deceased requested an autopsy due to ambiguous clinical signs before death. PD was confirmed by post-mortem examinations. Furthermore, signs of aspiration pneumonia and systemic arteriosclerosis were evident. However, histopathological analyses of the brain uncovered previously unsuspected findings, including acute vasculitis (predominantly lymphocytic) as well as multifocal necrotizing encephalitis of unknown etiology with pronounced inflammation including glial and lymphocytic reaction. In the heart, signs of chronic cardiomyopathy as well as mild acute lympho-histiocytic myocarditis and vasculitis were present. Although there was no history of COVID-19 for this patient, immunohistochemistry for SARS-CoV-2 antigens (spike and nucleocapsid proteins) was performed. Surprisingly, only spike protein but no nucleocapsid protein could be detected within the foci of inflammation in both the brain and the heart, particularly in the endothelial cells of small blood vessels. Since no nucleocapsid protein could be detected, the presence of spike protein must be ascribed to vaccination rather than to viral infection. The findings corroborate previous reports of encephalitis and myocarditis caused by gene-based COVID-19 vaccines.

For those not familiar with the medical lingo, necrotizing means tissue death and multifocal means “all over your brain.”

And “corroborate previous reports” means this is happening over and over again.

For more information

Here’s an article summarizing how vaccines can cause sudden death and the existing autopsy studies that predated this one. They all show the same thing and you see a lot from putting them all into context. This effect can be both sudden and delayed:

Here is the German study on this:

1. On COVID vaccines: why they cannot work, and irrefutable evidence of their causative role in deaths after vaccination(all 15 cases)
2. Video explanation of their findings(with English voiceover on the first 10 cases)

Their team was able to develop a way to test for spike protein in tissue and recently confirmed it was found in the tissues of vaccine victims.

Summary

In plain English, the vaccines can kill cells in your brain and your heart causing you to die.

Vaccines are never supposed to do that.

The CDC is silent on this and they’re not going to alert anyone. That’s the job of misinformation superspreaders such as myself.”

“A Case Report: Multifocal Necrotizing Encephalitis and Myocarditis after BNT162b2 mRNA Vaccination against COVID-19

by 

Michael Mörz

Institute of Pathology ’Georg Schmorl’, The Municipal Hospital Dresden-Friedrichstadt, Friedrichstrasse 41, 01067 Dresden, Germany

Academic Editor: Sung Ryul Shim

Vaccines 2022, 10(10), 1651; https://doi.org/10.3390/vaccines10101651 (registering DOI)

Received: 31 August 2022 / Revised: 25 September 2022 / Accepted: 27 September 2022 / Published: 1 October 2022

Abstract

The current report presents the case of a 76-year-old man with Parkinson’s disease (PD) who died three weeks after receiving his third COVID-19 vaccination. The patient was first vaccinated in May 2021 with the ChAdOx1 nCov-19 vector vaccine, followed by two doses of the BNT162b2 mRNA vaccine in July and December 2021. The family of the deceased requested an autopsy due to ambiguous clinical signs before death. PD was confirmed by post-mortem examinations. Furthermore, signs of aspiration pneumonia and systemic arteriosclerosis were evident. However, histopathological analyses of the brain uncovered previously unsuspected findings, including acute vasculitis (predominantly lymphocytic) as well as multifocal necrotizing encephalitis of unknown etiology with pronounced inflammation including glial and lymphocytic reaction. In the heart, signs of chronic cardiomyopathy as well as mild acute lympho-histiocytic myocarditis and vasculitis were present. Although there was no history of COVID-19 for this patient, immunohistochemistry for SARS-CoV-2 antigens (spike and nucleocapsid proteins) was performed. Surprisingly, only spike protein but no nucleocapsid protein could be detected within the foci of inflammation in both the brain and the heart, particularly in the endothelial cells of small blood vessels. Since no nucleocapsid protein could be detected, the presence of spike protein must be ascribed to vaccination rather than to viral infection. The findings corroborate previous reports of encephalitis and myocarditis caused by gene-based COVID-19 vaccines.”

Here is the German study mentioned by Steve Kirsch:

https://doctors4covidethics.org/wp-content/uploads/2021/12/end-covax.pdf

“On COVID vaccines: why they cannot work, and irrefutable evidence of their causative role in deaths after vaccination Sucharit Bhakdi, MD and Arne Burkhardt, MD

Why the vaccines cannot protect against infection A fundamental mistake underlying the development of the COVID-19 vaccines was to neglect the functional distinction between the two major categories of antibodies which the body produces in order to protect itself from pathogenic microbes. The first category (secretory IgA) is produced by immune cells (lymphocytes) which are located directly underneath the mucous membranes that line the respiratory and intestinal tract. The antibodies produced by these lymphocytes are secreted through and to the surface of the mucous membranes. 1 These antibodies are thus on site to meet air-borne viruses, and they may be able to prevent viral binding and infection of the cells. The second category of antibodies (IgG and circulating IgA) occur in the bloodstream. These antibodies protect the internal organs of the body from infectious agents that try to spread via the bloodstream. Vaccines that are injected into the muscle – i.e., the interior of the body – will only induce IgG and circulating IgA, not secretory IgA. Such antibodies cannot and will not effectively protect the mucous membranes from infection by SARS-CoV-2. Thus, the currently observed “breakthrough infections” among vaccinated individuals merely confirm the fundamental design flaws of the vaccines. Measurements of antibodies in the blood can never yield any information on the true status of immunity against infection of the respiratory tract. The inability of vaccine-induced antibodies to prevent coronavirus infections has been reported in recent scientific publications. The vaccines can trigger self-destruction A natural infection with SARS-CoV-2 (coronavirus) will in most individuals remain localized to the respiratory tract. In contrast, the vaccines cause cells deep inside our body to express the viral spike protein, which they were never meant to do by nature. Any cell which expresses this foreign antigen will come under attack by the immune system, which will involve both IgG antibodies and cytotoxic Tlymphocytes. This may occur in any organ. We are seeing now that the heart is affected in many young people, leading to myocarditis or even sudden cardiac arrest and death. How and why such tragedies might causally be linked to vaccination has remained a matter of conjecture because scientific evidence has been lacking. This situation has now been rectified. Histopathologic studies: the patients Histopathologic analyses have been performed on the organs of 15 persons who died after vaccination. The age, gender, vaccination record, and time of death after injection of each patient are listed in the table on the next page. The following points are of utmost importance: · Prior to death, only 4 of the 15 patients had been treated in the ICU for more than 2 days. The majority were never hospitalized and died at home (5), on the street (1), at work (1), in the car (1), or in home-care facilities (1). Therefore, in most cases, therapeutic intervention is unlikely to have significantly influenced the post-mortem findings. · Not a single death was brought into any possible association with the vaccination by the coroner or the public prosecutor; this association was only established by our autopsy findings. · The initially performed conventional post-mortems also uncovered no obvious hints to a possible role of vaccination, since the macroscopic appearance of the organs was overall unremarkable. In most cases, “rhythmogenic heart failure” was postulated as the cause of death. 2 But our subsequent histopathological analyses then brought about a complete turnaround. A summary of the fundamental findings follows. Case # Gender Age (years) Vaccine (injections) Time of death after last injection 1 female 82 Moderna (1. and 2.) 37 days 2 male 72 Pfizer (1.) 31 days 3 female 95 Moderna (1. and 2.) 68 days 4 female 73 Pfizer (1.) unknown 5 male 54 Janssen (1.) 65 days 6 female 55 Pfizer (1. and 2.) 11 days 7 male 56 Pfizer (1. and 2.) 8 days 8 male 80 Pfizer (1. and 2.) 37 days 9 female 89 Unknown (1. and 2.) 6 months 10 female 81 Unknown (1. and 2.) unknown 11 male 64 AstraZeneca (1. and 2.) 7 days 12 female 71 Pfizer (1. and 2.) 20 days 13 male 28 AstraZeneca (1.), Pfizer (2.) 4 weeks 14 male 78 Pfizer (1. and 2.) 65 days 15 female 60 Pfizer (1.) 23 days Histopathologic studies: findings Histopathologic findings of a similar nature were detected in organs of 14 of the 15 deceased. Most frequently afflicted were the heart (14 of 15 cases) and the lung (13 of 15 cases). Pathologic alterations were furthermore observed in the liver (2 cases), thyroid gland (Hashimoto’s thyroiditis, 2 cases), salivary glands (Sjögren`s Syndrome; 2 cases) and brain (2 cases). A number of salient aspects dominated in all affected tissues of all cases: 1. inflammatory events in small blood vessels (endothelitis), characterized by an abundance of Tlymphocytes and sequestered, dead endothelial cells within the vessel lumen; 3 2. the extensive perivascular accumulation of T-lymphocytes; 3. a massive lymphocytic infiltration of surrounding non-lymphatic organs or tissue with Tlymphocytes. Lymphocytic infiltration occasionally occurred in combination with intense lymphocytic activation and follicle formation. Where these were present, they were usually accompanied by tissue destruction. This combination of multifocal, T-lymphocyte-dominated pathology that clearly reflects the process of immunological self-attack is without precedent. Because vaccination was the single common denominator between all cases, there can be no doubt that it was the trigger of self-destruction in these deceased individuals. Conclusion Histopathologic analysis show clear evidence of vaccine-induced autoimmune-like pathology in multiple organs. That myriad adverse events deriving from such auto-attack processes must be expected to very frequently occur in all individuals, particularly following booster injections, is selfevident. Beyond any doubt, injection of gene-based COVID-19 vaccines places lives under threat of illness and death. We note that both mRNA and vector-based vaccines are represented among these cases, as are all four major manufacturers.”