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

Note: The story cites evidence that some cases occurred prior to Covid-19


 

In fact, it was one-month-ago, Critical Thinking & Reasoning posted this peer reviewed medical study,
authored by no-fewer than fifty virologist, epidemiologists, specialists, and other medical doctors. The study also has links to citations of other similar peer-reviewed studies. 

 CT&R Blogpost of  April 7th 2021

A short 5-10 minute read, I also have highlighted in red the most compelling evidence if time constrained:

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

 ...to Be Continued [1 PM May 7, 2021]


Okay, I am back after almost being mugged at the US Bank ATM located at 22nd and Mission; quick thinking to end the transaction led to a barrage of me being a "Bitch-Ass who ain't got no money, no how" as I fled the scene.

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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