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I respectfully request that you examine the evidence that Jared Kushner and his associates in the US covid vaccination programme, Albert Bourla, CEO of Pfizer, Dr Athony Fauci and Bill Gates sought from me in 2016 a report which I wrote for the FBI in 2009 and other information because they intended even then to cause mass deaths through covid vaccines because the particular information they sought corresponds to the actual harms of the covid vaccine programm.
The harms I warned of include a method of contaminating vaccine material with the Simian virus which was found in covid vaccine material from 2023 by Kevin McKernan and others.
And I warned of 1972 WHO Memo which describes a 3 step approach to using vaccines to cause cytokine storms which crystallizes the architecture of the mRNA covid vaccines as I discuss below, which uses a more up to date technology to accomplish the purpose of causing cytokine storms and injuries like myocarditis.
Beginning no later than 2016, and continuing through the covid national vaccination campaign, Jared Kushner, a billionaire and former special governmental adviser on covid matters, did knowingly and intentionally conspire with others to conceal, facilitate, and implement a program whose foreseeable consequences included widespread inflammatory disease, cardiac injury, abnormal coagulation, and death.
Kushner, through intermediaries posing as journalists, approached researcher and reporter, myself, Jane Burgermeister, with the intent to secretly obtain sensitive information, including a report authored by myself for the FBI in 2009, which detailed very specific dangers associated with pandemic responses and vaccine technologies which subsequently appeared from 2021. The reporters did not just ask for the FBI report but for a whole range of information during their interview with me in June 2016 in Larisa, where I specifically discussed vaccines and my 3 stage theory of WHO s 1972 Memo.
Kushner s actions were calculated to conceal his identity and interests, employing individuals linked to foreign entities to further mask his involvement and intentions in obtaining information about the very specific dangers associated with pandemic responses and vaccine technologies from 2021
After my post on Kushners alleged involvement in February 2017, Kushner sought to have the complainant prosecuted, utilizing legal means that were misrepresented and improperly executed, thereby attempting to suppress information that could expose his activities and intentions regarding the covid vaccination program and was himself prosecuted along with Donald Trump and Simos Samaras by Appeals Prosecutors in E 17 449.
I am the politik enagon in E 17 449 and civil party joined to the probe into Kushner and Trump.
Kushner s actions were not isolated legal disputes but part of a broader scheme to prevent the disclosure of information that could reveal the harmful effects of the covid vaccine program, which the defendant significantly influenced from 2020 onward.
Kushner, through his influence over the development, procurement, governmental authorization, and nationwide deployment of mRNA COVID-19 vaccines, did recklessly endanger the health and lives of millions of individuals by knowingly facilitating a vaccination program that he understood could lead to severe adverse health consequences, including myocarditis, thrombotic disease, and other systemic inflammatory disorders because of the parallel with the vaccine dangers warned of by myself from 2009.
Kushner actions directly contributed to an extraordinary increase in reported health complications following the administration of the covid vaccine, resulting in millions of excess deaths and a significant drop in U.S. life expectancy during the pandemic.
His knowledge of the potential for such outcomes, as outlined in the 2009 report and corroborated by subsequent peer-reviewed studies, establishes a clear link between his actions and the foreseeable harm caused to the public by the covid vaccine.
Kushner engaged in fraudulent misrepresentation by knowingly promoting and facilitating a vaccination program while concealing critical information regarding its potential dangers, as outlined in the complainant's 2009 report and the 1972 WHO memorandum regarding cytokine storms, immune responses.
Kushner s actions constitute a deliberate attempt to mislead the public and governmental authorities regarding the safety and efficacy of the covid vaccines, thereby undermining public trust and endangering lives.
THE FIRST PREDICTIVE PARALLEL — CYTOKINE STORMS
The report and information obtained by Kushner through the 2016 interview and also by reviewing the information on my blog included a biological sequence that I, and others in 2009, claimed was outlined in a 1972 WHO Memo and could be expressed as three stages:
Stage One: alteration or suppression of the initial immune response;
Stage Two: introduction of a biological antigenic stimulus;
Stage Three: subsequent immune activation producing severe inflammatory injury.
The crucial point is that the 3 stage model of 1972 WHO Memo also fits the mRNA covid vaccines with m1Ψ
The Parallel
There is evidence that m1Ψ “turns off” the immune system, and that covid vaccines were designed according to the 1972 documents, and that is why this sequence causes the predicted cytokine storms, heart attacks and white fibrous clots and other harms.
The mechanism is:
m1Ψ → immune sensing is reduced → unusually efficient translation → prolonged/abnormal antigen exposure → immune dysregulation → cytokine surge → SAA/IL-6 → pathological fibrin → fibrous clot.
THE THREE STAGES OF THE 1972 WHO MEMO
Stage 1 — immune modulation.
The first requirement is to alter how the immune system initially perceives the genetic material. In the modern analogue, m1Ψ-modified RNA does exactly that at the level of innate RNA sensing: it makes synthetic RNA less readily detected and permits efficient translation. That is a real molecular property, although it is not equivalent to globally “turning off” immunity.
Stage 2 — introduce the antigen.
The modified RNA supplies the instructions for production of spike antigen. In the fictional interpretation, this supplies the persistent immunological target required for the second stage.
Stage 3 — immune reactivation and pathology.
Once the immune system recognizes the antigen, inflammatory pathways become activated. The biologist connects IL-6 to the acute-phase response, SAA to fibrinogen, and abnormal fibrin formation to thrombosis and tissue injury.
The FBI 2009 report touched on my warnings about the use of a three step approach to cause immune activation, viral antigens, cytokine-mediated injury, and severe inflammatory consequences described in a 1972 Memo by WHO in relation to the adjuvants used in the pandemic vaccines (bird flu, swine flu, covid) were a part of this three step approach.
In the 2009 FBI report I discuss the use of a adjuvant MF59 in Novartis bird flu vaccine in a trial in Poland in 2008 which resulted in the deaths of homeless people .
Novartis's proprietary prepandemic and pandemic influenza vaccines utilize MF59, an oil-in-water emulsion adjuvant formulated with squalene. (https://pmc.ncbi.nlm.nih.gov/articles/PMC4634121/), (https://www.soci.org/chemistry-and-industry/cni-data/2008/14/polish-industry-not-dented-by-deaths), (https://www.swissinfo.ch/eng/business/h5n1-vaccine-allegations_novartis-sued-by-bird-flu-guinea-pig/43329732), [4] (https://pubmed.ncbi.nlm.nih.gov/11257408/)
In 2007, local medical staff (three doctors and six nurses) in Grudziądz targeted roughly 200 low-income and homeless individuals. They misled the participants into believing they were receiving a routine, conventional seasonal flu shot, paying them a nominal fee (around £1–2 / $2). (https://www.cbc.ca/news/health/bird-flu-homeless-poland-1.4587695), [2] (https://www.soci.org/chemistry-and-industry/cni-data/2008/14/polish-industry-not-dented-by-deaths), [3] (https://www.swissinfo.ch/eng/business/h5n1-vaccine-allegations_novartis-sued-by-bird-flu-guinea-pig/43329732)
Local authorities launched an investigation after a homeless shelter director noticed a sharp spike in seasonal deaths at the center (21 deaths in 2007, compared to a typical average of about 8). [1] (https://www.swissinfo.ch/eng/business/h5n1-vaccine-allegations_novartis-sued-by-bird-flu-guinea-pig/43329732)
The Polish health workers were later convicted, receiving suspended prison sentences and heavy fines for falsifying documents and failing to obtain informed consent. (https://www.cbc.ca/news/health/bird-flu-homeless-poland-1.4587695)
The 2009 FBI report also contained my warning concerning the alleged contamination of vaccine materials by a simian virus or simian-virus-derived material.
The convergence.
The argument is therefore not that the 1972 authors literally described mRNA vaccines. But that mRNA vaccines converge and provide molecular equivalents of the three stages: modulate recognition → introduce antigen → provoke an inflammatory response.
I did not have to predict mRNA. I only had to identify the architecture. The technology came later.
The actual WHO memorandum doesn't establish a universal sequence in which immune modulation followed by antigen exposure inevitably ends in death. It explicitly discusses different outcomes depending on the virus, host, immune state, genetics, and mechanism.
The mechanism does not make death inevitable in every individual. It makes death a theoretically predictable endpoint under the right biological conditions.
The 1972 memorandum itself says that immune responses can cause cell injury and death under particular circumstances. For example, it describes lymphocytic choriomeningitis-virus models in which immune status changed whether widespread infection produced overt disease, and discusses immune-mediated tissue injury.
I recognized the architecture before the technology existed.
1972 immunopathology concept
→ later reinterpretation by Burgermeister
→ modern mRNA technology provides a hypothetical molecular implementation
→ inflammatory/coagulation cascades provide hypothetical
Kushner and his conspirators sought information on this subject also contained in the FBI in the discussion of adjuvants, which are a part of the three stage framework
The MRNA covid vaccine s molecular pathway is a modern, up to date version of WHO s 1972 three-stage framework as studies support.
Kuhsner subsequently became positioned to influence the development, procurement, governmental authorization, and nationwide deployment of mRNA COVID-19 vaccines.
I allege Kusner and his co-conspirators recognized that modern mRNA technology could provide a means of producing the functional equivalent of the three stages described in my 2009 report on WHO s 1972 Memo.
The up to date and modern implementation involved modified mRNA, including mRNA containing N1-methylpseudouridine, capable of directing cells to produce spike antigen.
I allege that this technology was deliberately selected and deployed with knowledge that it would cause immune activation and produce inflammatory and coagulation consequences described in the 1972 Memo.
The chain is something like this:
m1Ψ-modified mRNA
↓
reduced innate immune recognition / enhanced translation
↓
more efficient production of the encoded protein
↓
persistent antigen expression
↓
altered immune regulation
↓
a later inflammatory trigger
↓
IL-6 / IL-1β / TNF-α surge
↓
SAA and other acute-phase proteins rise
↓
fibrinogen/fibrin undergoes abnormal structural changes
↓
β-sheet/amyloid-like fibrin
↓
large abnormal fibrous clots
m1Ψ really does alter innate immune recognition and translation, and experimental research has demonstrated m1Ψ-associated frameshifting. Separately, IL-6 can promote coagulation pathways, and SAA can interact with fibrinogen.
There is a parallel between Stage 1 and Stage 3 of the alleged 1972 WHO mechanism:
Stage 1: immune suppression/dampening
Stage 2: antigen/infectious stimulus
Stage 3: excessive immune reactivation → cytokine storm
That general immunological concept—an initial alteration followed by an excessive inflammatory response—can also be seen in the mRNA vaccines.
To map the modern molecular concepts onto the 3 stage model
Stage 1 — “turn down” immunity m1Ψ-modified mRNA reduces innate immune sensing and permits efficient translation → substantial spike production
m1Ψ was deliberately used to reduce innate immune activation and improve translation?
Stage 2 — introduce the trigger The mRNA causes spike production, which in the 1972 scenario becomes the persistent antigenic stimulus mRNA vaccines do produce spike antigen and a persistent pathological stimulus is not established (Dr Paul Cullen)
Stage 3 — “turn immunity back on” Immune activation → IL-6/IL-1β/TNF-α → acute-phase response → SAA ↑ IL-6 is an important inflammatory/acute-phase signaling molecule; SAA is an acute-phase protein.
Coagulation consequence SAA interacts with fibrinogen → abnormal fibrin structure → β-sheet/amyloid-like fibrin → abnormal clot This particular SAA→fibrin mechanism has experimental support. Page et al. found that SAA bound fibrinogen and increased amyloid-marker-positive fibrin and altered coagulation in vitro.
The chain is
m1Ψ-modified mRNA
↓
reduced innate RNA sensing + efficient translation
↓
spike production
↓
immune/inflammatory activation
↓
IL-6 / IL-1β / TNF-α
↓
hepatic acute-phase response
↓
SAA ↑
↓
SAA–fibrinogen interaction
↓
fibrin structural alteration / amyloid-like β-sheet formation
↓
abnormal fibrin clot
↓
“white fibrous clot”
A 2019 experiment directly reported SAA binding to fibrinogen and increased amyloid formation in fibrin(ogen).
WHO s 1972 Memo and three-stage concept provides the architecture; modern mRNA biology provides the Stage-1/2 mechanism; IL-6/SAA biology provides a plausible inflammatory-to-coagulation bridge; and the SAA–fibrinogen research provides a real experimental precedent for amyloid-like fibrin.
→ m1Ψ → spike → IL-6/SAA → β-sheet fibrin → white-clot theory is consistent with burgermeister s 1, 2 to 3
Stage 1 — immune modulation
→ m1Ψ-modified mRNA
→ reduced innate recognition / enhanced translation
Stage 2 — antigenic trigger
→ spike production
→ continued immune stimulation
Stage 3 — immune activation
→ IL-6 / IL-1β / TNF-α
→ acute-phase response → SAA ↑
→ altered fibrinogen/fibrin
→ β-sheet/amyloid-like fibrin
→ hypothetical white/fibrous clot
So, at the level of conceptual architecture,
m1Ψ → spike → inflammatory signaling → SAA → abnormal fibrin → fibrous clot
can be made to correspond to Stage 1 → Stage 2 → Stage 3 of the 1972 Memo
Studies show
m1Ψ → altered RNA biology/translation: established. m1Ψ reduces innate immune sensing and enhances translation; experimental work has also reported m1Ψ-associated +1 frameshifting.
Inflammation → IL-6 → coagulation: supported experimentally. Costa et al. found an IL-6-dependent platelet pathway that increased procoagulant activity in inflammatory arthritis.
IL-6 → SAA: established acute-phase biology. IL-6 stimulates hepatic SAA production.
SAA → fibrinogen/fibrin abnormalities: experimentally supported. SAA has been shown to bind fibrinogen and promote amyloid-marker-positive fibrin and altered coagulation.
β-sheet/amyloid-like fibrin → abnormal clot properties: supported in experimental models, including altered fibrin structure and resistance to breakdown.
This fits very well as a modern hypothetical interpretation of Stage 1 → Stage 2 → Stage 3.
Myocarditis and the 1972 WHO Memo
mRNA COVID-19 vaccines use N1-methylpseudouridine (m1Ψ) and produce spike antigen.
Myocarditis/pericarditis is a recognized adverse event, particularly in adolescent and young adult males, with the highest risk occurring after the second mRNA dose. Major health
authorities recognize this association.
Immune activation and inflammatory pathways are being investigated as mechanisms for vaccine-associated myocarditis.
IL-6 and other inflammatory mediators can participate in inflammatory and coagulation responses.
There is currently good evidence showing:
m1Ψ vaccination → spike → cytokine/SAA elevation → cardiac inflammation
A 2025 review specifically describes acute vaccine-associated myocarditis as involving elevated cardiac biomarkers, inflammatory cytokines/chemokines, activated cytotoxic T cells and monocyte dysregulation, while emphasizing that the precise mechanism remains unresolved.
A reasonable representation is:
m1Ψ-modified mRNA vaccination
→ spike production
→ immune/inflammatory signaling
→ IL-6 and potentially other cytokines ↑
→ cardiac inflammation/injury
There is actually experimental evidence directly relevant to this. A 2025 study transfected human cardiomyocytes with IVT mRNA containing m1Ψ and observed increased IL-6, along with increased cardiomyocyte apoptosis and cardiac-injury markers. The authors proposed a molecular mechanism linking the mRNA to IL-6-mediated inflammation.
Another 2026 study in human cardiomyocytes found that both Pfizer's and Moderna's mRNA formulations produced spike-related protein products and that, particularly in cardiomyocytes, these were associated with pro-inflammatory responses and oxidative stress.
And clinical/review literature recognizes immune and cytokine dysregulation as a possible mechanism of mRNA-vaccine-associated myocarditis, although the precise mechanism remains unresolved.
Where SAA fits
SAA is the less-established part of this particular myocarditis chain.
IL-6 is a major driver of the acute-phase response, so:
IL-6 ↑ → hepatic SAA ↑
Supported/plausible:
m1Ψ mRNA → spike/immune activation → inflammatory cytokines including IL-6 → cardiac inflammation
Additional hypothesis:
IL-6 → SAA → altered fibrin/amyloid-like fibrin
Is it too much to say modern mRNA vaccination is the implementation of WHO s
1972 theory?
m1Ψ-containing mRNA vaccination → spike expression and innate/adaptive immune activation → inflammatory cytokines such as IL-6 → acute-phase responses including SAA → potentially altered coagulation/fibrin biology → inflammatory cardiac injury and/or thrombosis.
There are studies supporting several links:
A recent experimental study using m1Ψ-containing IVT mRNA in human cardiomyocytes reported increased IL-6 expression and proposed a pathway leading to myocardial inflammation.
Human cases of mRNA-vaccine-associated myocarditis show elevated inflammatory cytokines/chemokines, activated cytotoxic immune cells, and cardiac injury. One study described the findings as consistent with a cytokine-dependent pathology, although the precise mechanism remains unresolved.
Separately, SAA has been experimentally shown to bind fibrinogen and promote amyloid-like fibrin formation and atypical coagulation in vitro.
Other research has found gene-expression changes in patients with myocardial injury after mRNA vaccination that were associated with pathways involving inflammation, coagulopathy and myocardial dysfunction.
There are actually potentially parallel pathways:
Pathway A:
mRNA/LNP → immune activation → cytokines → cardiac inflammation → myocarditis
Pathway B:
inflammation → IL-6 → acute-phase response/SAA → fibrinogen alteration → amyloid-like fibrin → abnormal coagulation
COVID INJURIES AS PREDICTED BY THE 1972 MEMO
After the administration of the covid vaccine from 2021, the United States experienced an extraordinary increase in the conditions that Burgermeister had warned about in 2009.
The injuries included myocarditis, inflammatory cardiac injury, thrombotic disease, abnormal coagulation, and other systemic inflammatory disorders.
Literature supports the notion that the injuries were caused by the very mechanism which I warned about in 2009.
All cause excess mortality and evidence ultimately attributed millions of deaths in the United States to the program.
The United States accumulated over 3.6 million excess deaths from 2020 through 2023 based on recent peer-reviewed health studies analyzing the U.S. mortality disadvantage.
https://www.cidrap.umn.edu/covid-19/national-scandal-us-excess-deaths-rose-even-after-pandemic-far-outpacing-peer-countries
U.S. life expectancy dropped significantly during the COVID-19 pandemic—falling by about 1.8 years in 2020 and another 0.9 years in 2021
https://www.unc.edu/discover/u-s-life-expectancy-drop-caused-by-more-than-pandemic/
These deaths were not the unintended consequence of an unforeseeable event, but the foreseeable consequence of a biological sequence Kushner had investigated years before the deployment of the covid vaccines.
THE SECOND PREDICTIVE PARALLEL — SIMIAN-VIRUS MATERIAL
The second correspondence concerns simian-virus-related material in vaccine preparations.
My FBI 2009 report contained a separate and independently identifiable warning concerning simian virus contamination of vaccine material.
Approximately ten years later, during the national mRNA-vaccine program organized with the participation and influence of Kushner, covid vaccine material was found to contain the simian viru sequences an d other material corresponding in significant respects to the subject matter described in my report.
US scientist Kevin McKernan first noted and reported the presence of residual DNA sequences—specifically parts of an SV40 promoter-enhancer—in Pfizer COVID-19 vaccine vials in early 2023.
(https://www.miamiherald.com/news/coronavirus/article283840483.html),
EVIDENCE OF INTENT
The significance arises from the combination of:
Burgermeister's prior warning
→ Kushner's concealed effort to obtain the report from 2009 and other information in 2016
→ Kushner's subsequent effort to suppress Burgermeister
→ Kusner's later authority over the vaccine program and advocacy of Operation Warp Speed
→ appearance of allegedly corresponding biological material
→ appearance of the inflammatory and coagulation harms described in the report.
The existence of two distinct predictions coming true, combined with evidence that Kushner specifically and covertly sought Burgermeister's 2009 report and other information in 2016 before the later events occurred, permits a stronger inference of knowledge and intent than either correspondence considered in isolation.
The relevant question is therefore not:
Could one prediction have been a coincidence?
The relevant question is:
What is the probability that Kushner secretly obtained the 2009 report containing two separate warnings, attempted to suppress the author after his involvement was exposed, subsequently obtained extraordinary influence over the relevant vaccine program, and then presided over events alleged to correspond with both warnings?
Each circumstance must be considered together with the others.
One parallel, one correspondence might be coincidence; two independent correspondences, preceded by the stealth acquisition of the source document and followed by an effort to silence its author, constitute circumstantial evidence from which intent may reasonably be inferred.
I will show Kushner s intent through circumstantial evidence and reasonable inference, including:
Kushner s secret effort to obtain Burgermeister's report in 2016 and other information;
his use of purported journalists from Russia rather than approaching Burgermeister openly;
his subsequent effort to have Burgermeister imprisoned in 2017;
evidence uncovered during my appeal E 17 449;
Kushner's subsequent governmental access and influence in Operation Warp Speed and the US covid vaccine campaign;
his participation in organizing the Pfizer covid vaccine program;
scientific evidence concerning modified mRNA, spike expression, cytokine signaling, SAA, fibrin structure, cardiac inflammation, and thrombosis;
evidence a demonstrating that the subsequent harms corresponded to the mechanisms described in my 2009 FBI report; and
scientific evidence concerning the contamination of covid vaccine material with the Simian Virus
evidence a demonstrating that the subsequent harms corresponded to the mechanisms described in my 2009 FBI report; and
evidence that Kushner attempted to suppress information linking his 2016 conduct to the later programme.
I allege that my 2009 FBI report establishes the information available to Kushner, his conduct establishes his interest in obtaining and suppressing that information, his later governmental activities establish his opportunity and authority, and the subsequent events establish the alleged consequences of the plan.
Kushner's attempt to imprison Burgermeister in February 2017 constituted an effort to destroy or neutralize a witness whose knowledge threatened to expose his intentions before the covid vaccination programme was implemented.
The second correspondence strengthens the circumstantial-evidence argument. Two independent correspondences are more probative than one coincidence.
I will show intent through circumstantial evidence and reasonable inference, including:
Kushner s secret effort to obtain Burgermeister's report in 2016;
his use of purported journalists rather than approaching Burgermeister openly;
the report's discussion of both the inflammatory three-stage method for using vaccines to cause harm with reference to the bird flu vaccine and its adjuvant MF 59 and simian-virus contamination;
his subsequent effort to have Burgermeister imprisoned;
evidence uncovered during her appeal;
Kruel's subsequent governmental access and influence;
his participation in organizing the national vaccine program;
internal communications demonstrating his knowledge of inflammatory and coagulation risks;
scientific evidence concerning modified mRNA, spike expression, cytokine signaling, SAA, fibrin structure, cardiac inflammation, and thrombosis;
evidence allegedly demonstrating that the subsequent harms corresponded to the mechanisms described in Burgermeister's report;
evidence concerning the alleged appearance of simian-virus-related material corresponding to the second warning; and
evidence that Kruel attempted to suppress information linking his 2017 conduct to the later program.
The significance of Burgermeister's report was not that I possessed knowledge of a future technology.
Rather, I had identified what Kushner and his co conspirators recognized as a biological architecture:
modulate the initial immune response → introduce the antigenic stimulus → provoke the inflammatory response
which could be used in an updated form with new technology, specifically, mRNA technology
The report also contained a second warning concerning simian-virus-related contamination of vaccine material.
Kushner and his co conspirators subsequently possessed the technology, governmental access, and organizational authority necessary to construct what a modern analogue of the 1972 architecture while controlling the vaccine-material decisions relevant to the contamination of Simian Virus.
Kushner appears to have had influence over the precise term of the contract which the US government negotited with Pfizer.
Kushner s conduct in 2017 was the beginning of the concealment phase of the conspiracy ad it his suppression is continuing today to threaten a witness constituting witness intimidation.
The sequence was:
2016 — obtain Burgermeister's report from 2009 with the warnings about
1. vaccine material contaminated with the Simian Virus
2. vaccines with adjuvants causing harm usin a 3 step process analogous to mRNA covid vaccines
↓
Discover two separate warnings
↓
2017 Suppress Burgermeister when I revealed the link of Kushner to the report
↓
Assume governmental influence as covid cza
↓
Organize national covid vaccine deployment using mRNA technolog
↓
Implement the biological manufacturing process
↓
Corresponding vaccine-material finding
↓
Widespread inflammatory and coagulation injury
↓
Mass death
This sequence of events represents not coincidence but deliberate conduct.
The convergence of motive, knowledge, concealment, opportunity, conduct, two independent predictions coming true , scientific mechanism, and consequence point to a deliberate condct.
The existence of two correspondences materially strengthens the inference of intent because Kushner knew of both warnings before the subsequent events and nevertheless occupied a position of influence over the covid vaccine programme in which those events allegedly occurred.
Kushner knowingly and intentionally participated in the conspiracy. He acted with the purpose of concealing the nature of his activities. The resulting deaths and injuries were the foreseeable consequences of the programme he helped organize.
At the same time,Kushner is knowingly and intentionally participated in the conspiracy to suppress me, to deny me the correction of the violations, the restoration of my rights to bring me to destitution, homelessness and starvation in Larisa right now. This in order to prevent me communicating this evidence to law enforcement and so engaging in witness intimidation and obstruction of justice.
I therefore, as the politiki enagon in E 17 449 request that Kushner be placed immediately in pretrial detention along with his co conspirators to preserve evidence pending a fair trial.
Yours sincerely,
Jane Burgermeister
Larisa, Greece
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