Covid MSM Narrative Collapsing Chronic Health Complications From Vaccines Skyrocketing AND Double Standard In TV News Reporting
Greetings Critical Thinking And Reasoning Companions,
Increasingly, people are in what appears to me to be or what can best be characterized as a global pandemic of Stockholm Syndrome.
Despite all of the web-based news reports of the vaccines severely altering women's periods/cycle [many contend a depopulation agenda is underway using vaccines that make it no longer possible for a new life/zygote to successfully attach itself to the woman's uterus--among other severe side-effects now being documented.] Unfortunately, this subject continues to be framed as "vaccine hesitancy" generated by "Internet conspiracy theorist!"
Again, despite all of the reports of sudden death--especially after receiving the second Pfizer jab--and these seizure progressing into Mad Cow disease-type neurological disorders, there is little discussion on what is occurring by the dinosaur press.
Unfortunately, the television network affiliates in this Top 5 TV Market--The San Francisco Bay Area--remain clueless repeaters continuing to promote the need to be vaccinated, and obfuscating that most all of these horrific attacks on Asians are perpetrated by black men.
Why?
I contend if it does not fit the "Old White Male's are responsible for this shooting or that school shooting." Oftentimes, coverage soon after the daily news-cycle is suspended if the suspect arrested, killed, or carrying-out the school shooting or knife attack is of an ethnicity deemed not worthy of continued coverage--not fitting their MSM narrative to keep us whipped-up and fighting among ourselves, time and again.
Notice how there are delays regarding posting a booking photo of some suspects if they do not fit that above narrative.
Since I Am Wearing My Media Analyst Hat
Let me point to the idiocy that passes for TV News coverage spewing from what we called growing-up, the idiot box:
Question: Anchor says to Co Anchor, "What is causing this lumber shortage that has tripled the price?"
Answer: The diversion of supply to board-up, take-down, board-up again....and again, the many stores, restaurants, and obvious targets of anger such as the corporate headquarters of Twitter, UBER; for the same reason, Fortune 500 and NASDAQ tech headquartered companies, locally, in The Financial District and SOMA. This, not just major population centers in the Bay Area but throughout the nation.
Q: "How can we explain this sharp-rise in crime, and why the murder-rate has tripled in so many of our major urban centers?"
A: Before the initiating of an almost year long orgy of rioting and arson, George Soros funded DA's had been strategically placed to release and/or not charge violent criminals to add to the mayhem in this take-down of the US and Western Civilization; disguised in catch-phrases of judicial reform, no cash bail reform, and creating more equity as We Build Back Better, releasing all of these felons in penitentiaries due to Covid was also a swell idea, right?
Buy more deadbolts and firearms now, because it has been announced that some 76,000 inmates are to be released soon, including those with life sentences, here in California:
May 1, 2021 LA Times: More Inmates to Be Released for "Good Behavior"
And my favorite...
Q: Why have prices at the pump gone through the roof ?
A: Ahh...On January 20th upon inauguration, President Biden signed executive orders shutting down completion of the Keystone pipeline--shifting the transportation of crude back to Globalist Billionaire, Warren Buffets, Burlington Northern Santa Fe Railway; this, accomplished by also ordering a huge reduction in domestic oil production--we had become the largest net exporter of oil surpassing Saudi Arabia in recent years--to meet the administrations climate-change agenda.
Enough Q & A: Wrapping-up on The Media & Taking A Second Look At A Peer Reviewed Medical Study Hypothesizing Covid-19 is A Bio Weapon
Clearly, the news-cycle has become so toxic, fast and furious, and filled with story after story of peoples' derangement, I hesitate even writing about race-relations, lest I am interpreted of writing something improper; on the other hand, it took two-and-a-half days for the majority of our local TV network affiliates to show the man accused in the recent stabbing of two elderly Chinese-Americans at a MUNI transit platform, I had just been standing-on moments earlier at 4th and Market Street.
It reminds me of the constant ranting from my professors--picked-up and parroted by many of my student Mass Communication major colleagues at SFSU--about the under representation or opportunities for minorities--especially black and Latino women in broadcast and electronic media.
I am going to solidify my assertion and move-on as I am burying-the-lead as we say in my quasi-journalism world. However, this does tie-in with the constant censorship-by-omission exhibited by these top-tier TV editors, reporters, and local anchor persons; daily, I have various radio broadcasts on, TV broadcasts alternating to different channels every few hours/days, and stream several programs--some silencing audio on my laptop back & forth oftentimes viewed in split-screen, simultaneously.
In other words, my place resembles a citizen journalism-lite radio or television newsroom buzzing with breaking news.
Point being, there is an abundance of diversity & representation of syndicated TV personalities, guest, and co-hosts, especially throughout the daytime television line-up.
The majority are people of color, representing many--if not all--of different ethnic backgrounds, women over-represented, and indisputably, plenty of LBGTQ types, abound. For instance, local TV news teams recent decisions on hiring extremely obese women of color have them also now well represented; clearly, local on-air TV media is as diverse as the Bay Area's populace.
Local TV Gets an A' for Diversity & a D' for NOT Covering Vaccine Side-effects AND Deaths
Let us get started on the meat of this post on what appears to be the first evidence of a large spike of Prions disease since vaccination really kicked-in big-time, four or five months ago:
BBC May 5th 2021: Doctors Investigate Mysterious Brain Disease in Canada
CT&R Blogpost of April 7th 2021
Volume
5 | Issue 1 | 1 of 3Microbiol Infect Dis, 2021
COVID-19 RNA Based Vaccines and
the Risk of Prion Disease
Classen
Immunotherapies, Inc., 3637 Rockdale Road, Manchester, MD 21102, E-mail:
classen@vaccines.net.J. Bart
Classen, MD*Citation: Classen
JB. COVID-19 RNA Based Vaccines and the Risk of Prion Disease.
Microbiol
Infect Dis. 2021; 5(1): 1-3.Research ArticleABSTRACT
Development
of new vaccine technology has been plagued with problems in the past. The
current RNA based SARS-CoV-2 vaccines were approved in the US using an
emergency order without extensive long term safety testing. In this paper
the Pfizer COVID-19 vaccine was evaluated for the potential to induce
prion-based disease in vaccine recipients. The RNA sequence of the vaccine
as well as the spike protein target interaction were analyzed for
the potential to convert intracellular RNA binding proteins TAR DNA
binding protein (TDP-43) and Fused in Sarcoma (FUS) into their pathologic
prion conformations. The results indicate that the vaccine RNA has specific
sequences that may induce TDP-43 and FUS to fold into their pathologic
prion confirmations. In the current analysis a total of sixteen UG tandem
repeats (ΨGΨG) were identified and additional UG (ΨG) rich sequences were
identified. Two GGΨA sequences were found. Potential G Quadruplex
sequences are possibly present but a more sophisticated computer program
is needed to verify these. Furthermore, the spike protein, created by the
translation of the vaccine RNA, binds angiotensin converting enzyme 2
(ACE2), a zinc containing enzyme. This interaction has the potential to increase
intracellular zinc. Zinc ions have been shown to cause the transformation of
TDP-43 to its pathologic prion configuration.
The
folding of TDP-43 and FUS into their pathologic prion confirmations is known to
cause ALS, front temporal lobar degeneration, Alzheimer’s disease and
other neurological degenerative diseases. The enclosed finding as well as
additional potential risks leads the author to believe that regulatory approval
of the RNA based vaccines for SARS-CoV-2 was premature and that the
vaccine may cause much more harm than benefit.*Correspondence:J. Bart Classen, MD, Classen Immunotherapies,
Inc., 3637 Rockdale Road, Manchester, MD 21102, Tel:
410-377-8526.Received:27 December 2020; Accepted: 18 January 2021
Microbiology
& Infectious Diseases ISSN
2639-9458KeywordsCOVID-19, Vaccines, Diabetes,
Immunity.Introduction:
Vaccines
have been found to cause a host of chronic, late developing adverse
events. Some adverse events like type 1 diabetes may not occur until 3-4
years after a vaccine is administered [1]. In the example of type 1 diabetes the
frequency of cases of adverse events may surpass the frequency of cases of
severe infectious disease the vaccine was designed to prevent. Given that type 1 diabetes
is only one of many immune mediated diseases potentially caused
by vaccines, chronic late occurring adverse events are a serious
public health issue.The advent of new vaccine technology creates new
potential mechanisms of vaccine adverse events. For example, the
first killed polio vaccine actually caused polio in recipients
because the up scaled manufacturing process did not effectively kill the
polio virus before it was injected into patients. RNA based vaccines
offers special risks of inducing specific adverse events.
One
such potential adverse event is prion based diseases caused by activation
of intrinsic proteins to form prions. A wealth of knowledge has been
published on a class of RNA binding proteins shown to participating in
causing a number of neurological diseases including Alzheimer’s disease
and ALS. TDP-43 and FUS are among the best studied of these proteins
[2].The Pfizer RNA based COVID-19 vaccine was approved by the US FDA under
an emergency use authorization without long term safety data. Because of
concerns about the safety of this vaccine a study was performed to
determine if the vaccine could potentially induce prion based disease.MethodsPfizer’s RNA based vaccine
against COVID-19 was evaluated for the potential to convert TDP-43 and or
FUS to their prion based Volume 5 | Issue 1 | 2 of 3Microbiol Infect Dis, 2021disease causing states. The
vaccine RNA was analyzed for the presence of sequences that can activate
TDP-43 and FUS. The interaction of the transcribed spike protein with its
target was analyzed to determine if this action could also activate
TDP-43 and FUS.ResultsAnalysis of the Pfizer vaccine
against COVID-19 identified two potential risk factors for inducing prion
disease is humans.
The
RNA sequence in the vaccine [3] contains sequences believed to
induce TDP-43 and FUS to aggregate in their prion based
conformation leading to the development of common neurodegerative diseases. In
particular it has been shown that RNA sequences GGUA [4], UG rich
sequences [5], UG tandem repeats [6], and G Quadruplex sequences [7], have
increased affinity to bind TDP-43 and or FUS and may cause TDP-43 or FUS
to take their pathologic configurations in the cytoplasm. In the current
analysis a total of sixteen UG tandem repeats (ΨGΨG) were identified and
additional UG (ΨG) rich sequences were identified. Two GGΨA
sequences were found. G Quadruplex sequences are possibly present but sophisticated
computer programs are needed to verify these.The spike protein encoded by the
vaccine binds angiotensin converting enzyme 2 (ACE2), an enzyme which
contains zinc molecules [8]. The binding of spike protein to ACE2 has
the potential to release the zinc molecule, an ion that causes
TDP-43 to assume its pathologic prion transformation [9].DiscussionThere is an old saying in
medicine that “the cure may be worse than the disease.” The phrase can be
applied to vaccines. In the current paper the concern is raised that the
RNA based COVID vaccines have the potential to cause more disease than
the epidemic of COVID-19. This paper focuses on a novel
potential adverse event mechanism causing prion disease which could
be even more common and debilitating than the viral infection
the vaccine is designed to prevent.
While
this paper focuses on one potential adverse event there are multiple other
potential fatal adverse events as discussed below. Over the last two decades there
has been a concern among certain scientists that prions could be used as
bioweapons. More
recently there has been a concern that ubiquitous intracellular
molecules could be activated to cause prion disease including
Alzheimer’s disease, ALS and other neurodegenerative diseases. This
concern originates due to potential for misuse of research data on
the mechanisms by which certain RNA binding proteins like TDP-43, FUS
and others can be activated to form disease causing prions. The fact that this research,
which could be used for bioweapons development, is funded by private
organizations including the Bill and Melinda Gates Foundation, and Ellison
Medical Foundation [2] without national/international oversight is also a
concern.
In the
past, for example, there were prohibitions for publishing information
pertaining to construction of nuclear bombs.Published data has shown that there
are several different factors that can contribute to the conversion of
certain RNA binding proteins including TDP-43, FUS and related molecules
to their pathologic states. These RNA binding proteins have many functions
and are found in both the nucleus and the cytoplasm. These binding
proteins have amino acid regions, binding motifs that bind specific
RNA sequences. Binding to certain RNA sequences when the proteins are
in the cytoplasm is believed to causes the molecules to fold in certain
ways leading to pathologic aggregation and prion formation in the
cytoplasm [2]. The
current analysis indicates Pfizer's RNA based COVID-19 vaccine contains
many of these RNA sequences that have been shown to have high affinity for
TDP-43 or FUS and have the potential to induce chronic degenerative
neurological diseases.Zinc binding to the RNA recognition motif of TDP-43 is
another mechanism leading to formation of amyloid like aggregations
[9]. The viral spike protein, coded by the vaccine RNA sequence,
binds ACE2 an enzyme containing zinc molecules [8]. This
interaction has the potential to increase intracellular zinc levels
leading to prion disease. The initial binding could be between spike
proteins on the surface of the cell transfected by the vaccine and
ACE2 on the surface of an adjacent cell. The resulting complex
may become internalized.
Alternatively,
the interaction could initially take place in the cytoplasm of a cell that
makes ACE2 and has been transfected with the vaccine RNA coding for the
spike protein. The
interaction is quite concerning given the belief that the virus causing
COVID-19, SARS-CoV-2, is a bioweapon [10,11] and it is possible that the
viral spike protein may have been designed to cause prion disease.Another related concern is
that the Pfizer vaccine uses a unique RNA nucleoside
1-methyl-3'-pseudouridylyl (Ψ). According to FDA briefing documents, this
nucleoside was chosen to reduce activation of the innate immune system
[12]. RNA molecules containing this nucleoside will undoubtedly have
altered binding [13]. Unfortunately, the effect on TDP-43, FUS and other
RNA binding proteins is not published. The use of this nucleoside
in a vaccine can potentially enhance the binding affinity of
RNA sequences capable of causing TDP-43 and FUS to assume
toxic configurations.
There
are many other potential adverse events that can be induced by the novel
RNA based vaccines against COVID-19. The vaccine places a novel molecule,
spike protein, in/on the surface of host cells:
This
spike protein is a potential receptor for another possibly novel
infectious agent. If
those who argue that the COVID-19 is actually a bioweapon are correct,
then a second potentially more dangerous virus may be released that binds
spike protein found on the host cells of vaccine recipients. Data is not publicly
available to provide information on how long the vaccine RNA is
translated in the vaccine recipient and how long after translation the
spike protein will be present in the recipient’s cells. Such
studies pertaining to in vivo expression will be complex and
challenging. Genetic diversity protects species from mass casualties
caused by infectious agents.
One
individual may be killed by a virus while Volume 5 | Issue 1 | 3 of 3Microbiol Infect Dis,
2021another
may have no ill effects from the same virus. By placing the identical
receptor, the spike protein, on cells of everyone in a population, the
genetic diversity for at least one potential receptor disappears. Everyone
in the population now becomes potentially susceptible to binding with the
same infectious agent.Autoimmunity and the opposing condition, metabolic
syndrome, are well know adverse events caused by vaccines [14]. COVID-19 infections
are associated with the induction of autoantibodies and autoimmune disease
[15,16] making it more than plausible a vaccine could do the same. One
author has found amino acid sequences coded by the spike protein to be
identical to sequences in human proteins including proteins found in the
CNS [17]. Autoimmunity can also be induced by epitope spreading when
a foreign antigen, like the spike protein, is presented by an
antigen presenting cell that also has self molecules attached to its MHC molecules.
Finally,
others working in the field have published additional support that
COVID-19 vaccines could potentially induce prion disease. Authors [18]
found prion related sequences in the COVID-19 spike protein which were not
found in related coronaviruses. Others [19] have reported a case of prion
disease, Creutzfeldt-Jakob disease, initially occurring in a man with
COVID-19.
Many have
raised the warning that the current epidemic of COVID-19 is actually the
result of an bioweapons attack released in part by individuals in the
United States government [10,11]. Such a theory is not far fetched given
that the 2001 anthrax attack in the US originated at Fort Detrick, a US
army bioweapon facility. Because the FBI’s anthrax investigation was
closed against the advice of the lead FBI agent in the case, there are
likely conspirators still working in the US government. In such a scenario
the primary focus of stopping a bioweapons attack must be to apprehend
the conspirators or the attacks will never cease. Approving a vaccine, utilizing
novel RNA technology without extensive testing is extremely dangerous. The
vaccine could be a bioweapon and even more dangerous than the original
infection.
The Below Footnoted Citations
Can be Accessed for Further Confirmation
...Or, Scroll Past for A :35m
Video of the Blueprint for the Planedemic Written Four/Five years ago
References1. Classen JB, Classen DC.
Clustering of cases of insulin dependent diabetes (IDDM) occurring three
years after Hemophilus influenza B (HiB) immunization support
causal relationship between immunization and IDDM.
Autoimmunity. 2002; 35: 247-253.2. King OD, Gitler AD, Shorter J. The
tip of the iceberg: RNA-binding proteins with prion-like domains in
neurodegenerative disease. Brain Res. 2012; 1462: 61-80.3. WHO,
International Non Proprietary Names Program: 11889. 9/2020.4. Kapeli
K, Pratt GA, Vu AQ, et al. Distinct and shared functions of ALS-associated
proteins TDP-43, FUS and TAF15 revealed by multisystem analyses. Nature
Communications. 2016; 7: 12143.5. Kuo P, Chiang C, Wang Y, et al. The
crystal structure of TDP-43 RRM1-DNA complex reveals the specific recognition
for UG- and TG-rich nucleic acids. Nucleic Acids Research. 2014; 42:
4712-4722.6. Tollervey JR, Curk T, Rogelj B, et al. Characterizing the
RNA targets and position-dependent splicing regulation by
TDP-43; implications for neurodegenerative diseases. Nat
Neurosci. 2011; 14: 452-458.7. Imperatore JA, McAninch DS,
Valdez-Sinon AN, et al. FUS recognizes G quadruplex structures within
neuronal mRNAs. Frontiers in Molecular Biosciences. 2020; 7:
6.8. Shang J, Ye G, Shi K, et al. Structural basis of
receptor recognition by SARS-CoV-2. Nature. 2020; 581: 221-225.9. Garnier
C, Devred F, Byrne D, et al. Zinc binding to RNA recognition motif of
TDP-43 induces the formation of amyloid-like aggregates. Sci Rep. 2017; 7:
6812.10. Classen JB. COVID-19, MMR vaccine, and bioweapons. Diabetes &
its Complications.2020; 4: 1-8.11. Classen JB. Evidence supporting the
hypothesis that the 2019 epidemic of E-vaping acute lung injury (EVALI)
was caused in part by COVID-19. Diabetes & Complications. 2020; 4:
1-2.12. Pfizer-Biotech: COVID-19 Vaccine (BNT162, PF-07302048), Vaccines
and Related Biological Products Advisory Committee Briefing Document.
Meeting Date: 10 December 2020.13. Roundtree IA, Evans ME, Pan, et al.
Dynamic RNA modifications in gene expression regulation. Cell. 2017;
169: 1187-1200.14. Classen JB. Review of Vaccine Induced Immune
Overload and the Resulting Epidemics of Type 1 Diabetes and
Metabolic Syndrome, Emphasis on Explaining the Recent accelerations
in the Risk of Prediabetes and other Immune Mediated Diseases. J Mol
Genet Med. 2014; S1: 025.15. Amiral J. Can COVID-19 Induce an autoimmune
disease associated with long- lasting symptoms and
delayed complications? Ann Clin Immunol Microbiol. 2020; 2:
1014.16. Wang EY, Mao T, Klein J, et al. Diverse functional
autoantibodies in patients with COVID-19. medRxiv preprint.
2020.17. Lyons-Weiler J. Pathogenic priming likely contributes to
serious and critical illness and mortality in COVID-19 via
autoimmunity. Journal of Translational Autoimmunity. 2020; 3:
100051.18. Tetz G, Tetz V. SARS-CoV-2 prion-like domains in
spike proteins enable higher affinity to ACE2. Preprint.
2020.19. Young MJ, O’Hare M, Matiello M, et al.
Creutzfeldt-Jakob disease in a man with COVID-19:
SARS-CoV-2-accelerated neuro degeneration? Brain, Behavior, and Immunity.
2020; 89: 601-603.© 2021
Classen JB. This article is distributed under the terms of the Creative Commons
Attribution 4.0 International License
BREAKING: May 7, 2021 SAN FRANCISCO KRON 4 (18:00 PDT)
Apparently, there is no real concern about the suspect in the recent stabbing of two elderly Asian women at 4th & Market not appearing in court today.
Was he released? Why is this not the top story?
Following-up with KPIX 5 site online, the suspect appears to still be in custody but did not feel like appearing in court.
WTF?
Since when do violent criminals in custody decide, "Nah, not really feeling it, today, court-wise."
MORE TROUBLING LIFE-LONG DEFENSE ATTORNEY--SF DA FACING A RECALL EFFORT--CHESA BOUDIN, PLANS TO BE THE ATTORNEY PROSECUTING THE CASE
What could possibly go wrong, right?
Here is an excerpt from the recent KPIX 5 online site. KRON at 8 PM continues to be not forthcoming on the story:
KPIX 5 learned from a police source on Wednesday that Thompson has a long and troubled criminal
history,
with more than two dozen arrests in the last 20 years. He was placed under
a psychiatric hold at least once and, in 2019, was arrested for battery.
KPIX 5 also learned that in 2017, Thompson was arrested for stabbing a person
at this homeless shelter on 5th and Bryant Streets with a pair of scissors.
Police say it was another unprovoked attack.READ MORE:Miles
Hall Shooting: No Charges Against Walnut Creek Police Officers In 2019 Killing
The
DA’s office said Thompson’s last arrest was in April of 2020, when a judge
issued an arrest warrant for missing court. When he was arrested on that
warrant, he was in possession of a drug pipe.
The San Francisco Police Officers Association, which has been critical of
Boudin in the past, on Friday issued a press release alleging that Thompson’s
2017 arrest was in connection with an unprovoked stabbing, similar to the most
recent case.
“This is Chesa Boudin’s San Francisco, where repeat offenders get second,
third, and fourth chances while victims are left bleeding in our streets,” the
SFPOA said. “Boudin’s latest blunder is shameful, and his catch and release
policies for violent criminals are leading to more and more victims. We have
had enough.”
President of the San Francisco Police Officers Association Tony Montoya leveled
additional criticism at Boudin, calling his participation in the case a stunt.
“To date, this is Chesa’s most disrespectful political stunt. The victims in this case and their families deserve the most experienced violent crime prosecutor in court today and not a criminal defense attorney with zero experience prosecuting any crime,” Montoya said in the release.
CLARIFICATION: Finally, tonight, just prior to 21:00 PM Pacific Daylight Time, KRON 4 has clarified that the stabbing suspect remains in custody without bail.
And I will Leave You With An Example of Globalists Hiding Things In The Open
Newsweek April, 20, 2020: Fauchi Backed US $$$ To Fund Wuhan Lab
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