>>18240288 (lb)
>shill
Kek!
Miss me with that bullshit.
re:
>>18240277 (lb)
Evidence for a connection between coronavirus disease-19 and exposure to radiofrequency radiation from wireless communications including 5G
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580522/
Abstract
Background and Aim:
Coronavirus disease (COVID-19) public health policy has focused on the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus and its effects on human health while environmental factors have been largely ignored. In considering the epidemiological triad (agent-host-environment) applicable to all disease, we investigated a possible environmental factor in the COVID-19 pandemic: ambient radiofrequency radiation from wireless communication systems including microwaves and millimeter waves. SARS-CoV-2, the virus that caused the COVID-19 pandemic, surfaced in Wuhan, China shortly after the implementation of city-wide (fifth generation [5G] of wireless communications radiation [WCR]), and rapidly spread globally, initially demonstrating a statistical correlation to international communities with recently established 5G networks. In this study, we examined the peer-reviewed scientific literature on the detrimental bioeffects of WCR and identified several mechanisms by which WCR may have contributed to the COVID-19 pandemic as a toxic environmental cofactor. By crossing boundaries between the disciplines of biophysics and pathophysiology, we present evidence that WCR may: (1) cause morphologic changes in erythrocytes including echinocyte and rouleaux formation that can contribute to hypercoagulation; (2) impair microcirculation and reduce erythrocyte and hemoglobin levels exacerbating hypoxia; (3) amplify immune system dysfunction, including immunosuppression, autoimmunity, and hyperinflammation; (4) increase cellular oxidative stress and the production of free radicals resulting in vascular injury and organ damage; (5) increase intracellular Ca2+ essential for viral entry, replication, and release, in addition to promoting pro-inflammatory pathways; and (6) worsen heart arrhythmias and cardiac disorders.
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Conclusion
There is a substantial overlap in pathobiology between COVID-19 and WCR exposure. The evidence presented here indicates that mechanisms involved in the clinical progression of COVID-19 could also be generated, according to experimental data, by WCR exposure. Therefore, we propose a link between adverse bioeffects of WCR exposure from wireless devices and COVID-19.
Specifically, evidence presented here supports a premise that WCR and, in particular, 5G, which involves densification of 4G, may have exacerbated the COVID-19 pandemic by weakening host immunity and increasing SARS-CoV-2 virulence by (1) causing morphologic changes in erythrocytes including echinocyte and rouleaux formation that may be contributing to hypercoagulation; (2) impairing microcirculation and reducing erythrocyte and hemoglobin levels exacerbating hypoxia; (3) amplifying immune dysfunction, including immunosuppression, autoimmunity, and hyperinflammation; (4) increasing cellular oxidative stress and the production of free radicals exacerbating vascular injury and organ damage; (5) increasing intracellular Ca2+ essential for viral entry, replication, and release, in addition to promoting pro-inflammatory pathways; and (6) worsening heart arrhythmias and cardiac disorders.
WCR exposure is a widespread, yet often neglected, environmental stressor that can produce a wide range of adverse bioeffects. For decades, independent research scientists worldwide have emphasized the health risks and cumulative damage caused by WCR [42,45]. The evidence presented here is consistent with a large body of established research. Healthcare workers and policymakers should consider WCR a potentially toxic environmental stressor. Methods for reducing WCR exposure should be provided to all patients and the general population.
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MORE at pdf sauce
https://www.thegatewaypundit.com/2023/01/19-year-old-wsu-student-found-dead-dorm-no-evidence-foul-play-involved/
19-Year-Old WSU Student Found Dead in His Dorm – No Evidence of Foul Play Involved
A freshman student from Washington State University (WSU) was found dead in his dorm room on Sunday, Jan. 22.
At approximately 1:30 p.m. on Sunday, a male student was found dead in his dorm room at Perham Hall on the Pullman campus, according to WSU police Assistant Chief Dawn Daniels.
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The student was later identified by the Whitman County Coroner’s Office as 19-year-old Luke Morgan Tyler.
Chief Gary Jenkins of the WSU Police Department stated it would be premature to speculate on the cause of death until the investigation is completed.
TRENDING: WATCH: "What About The $80,000 For Alcohol?" - Ronna Romney McDaniel Runs From TGP Reporter When Asked About Spending Millions On Luxury Items Before RNC Chair Election In Dana Point, CA
According to the police, there is no evidence of foul play involved in Tyler’s death.
According to Jenkins, the WSU Police Department is conducting an investigation into the circumstances surrounding Tyler’s death in coordination with the Whitman County Coroner.
“It’s worth mentioning that there has been a significant amount of conjecture regarding the circumstances surrounding this incident and the actual cause of the student’s passing. I would caution the public against speculation at this point in the investigation,” said Phil Weiler, Vice President at Washington State University.
“The facts in this case are still being gathered. It could be several weeks before the coroner’s office determines the cause and manner of death. We want to ensure that the investigation can proceed unimpeded,” Weiler continued.
According to Spokesman, nearly 8,000 people had signed a petition created by Tyler’s friends on Wednesday evening, demanding that Tyler’s fraternity, Theta Chi, be investigated in connection with his death.
A fundraising campaign was created to cover the cost of Luke’s funeral for his family. You can help donate here.
WSU Chancellor Elizabeth S. Chilton issued the following statement via KREM 2:
“Dear Cougs,
I continue to be heartbroken over the student death that occurred in a residence hall on our campus over the weekend. The loss of a member of our Cougar family creates a tremendous loss for all of us, and I want to extend my deepest condolences to the student’s family, friends, classmates, and fellow Cougs.
In the tragic case of any student death, WSU has a strict protocol to follow with procedures that were put in place out of respect for both the families and the investigative process. Arguably the most important element of this protocol is the direct outreach from our Dean of Students Office to the family and friends of the decedent. I’m very thankful for the incredible work and ongoing support services provided by our Dean of Students in this case, and overall.
WSU Pullman will not release any information about the individual until details have been coordinated with the family and the Whitman County Coroner’s Office. We will always maintain a high level of respect for both the families and investigative process, and will not disclose any information that could inadvertently disrupt this process.
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I understand that during trying times a lack of information often leads to confusion and questions. I urge everyone to avoid speculation about this incident so that the investigation may proceed unimpeded. We anticipate that the coroner’s office will release more information, including the cause and manner of death, in the coming weeks.
As we all process this tragic incident, I want to remind everyone that we are here for you, and that support services are available. Please visit our Crisis Support Resources page to learn more.”
https://twitter.com/AndyGreensky/status/1618874398844256256
Andy Greensky
@AndyGreensky
Bill Gates criticized the Ukrainian government
"The Ukrainian government is one of the worst in the world… Corrupt, controlled by a few rich people. Indeed, unfortunately for the people of Ukraine," the businessman said.
It seems that Zelensky's watch is moving towards midnight
The Washington Post
@washingtonpost
Breaking news: Monogamous gay and bisexual men will be allowed to donate blood under planned FDA guidance, easing decades-long restrictions. New rules will focus on sexual behaviors, regardless of gender, that pose a higher risk of transmitting HIV.
https://twitter.com/washingtonpost/status/1618740399387852803
don't go in for surgery without banking your own blood first…
https://twitter.com/TheChiefNerd/status/1618739451878080512
Chief Nerd
@TheChiefNerd
🚨 JUST IN: As Today's VRBPAC Meeting Ended, CDC Dep. Dir. Tom Shimabukuro Admits COVID Vaccines Are Causing "Debilitating Illnesses"
"We are aware of these reports of people experiencing long-lasting health problems following COVID vaccination"
@SenRonJohnson
@RepThomasMassie
https://mobile.twitter.com/Parsifaler/status/1618981262957625344
Walter M Chesnut
@Parsifaler
The more I study SARS-CoV-2 and its Spike Protein, the more I am stunned. I have never seen anything like it. A virus with a viral protein that appears to cause DNA translation machinery to intentionally make lethal errors. Hypotheses>link below.
Recall in the beginning anons noticing that smokers did not seem get covid at the rates of non-smokers?
Consider in the past decade the move to stop making smoking cool, moving to vaping and weed smoking.
Now consider the well-known American medicine plant tobacco, and it's active ingredient- nicotine.
Friday Hope: Nicotinamide Riboside: A Compound Which Facilitates DNA Damage (Mistranslation) Repair
A Potential Powerful Therapeutic for COVID, Long COVID and Spike Protein Progeria Disease
While studying the pathology of the Spike Protein, I am equally committed to studying ways to combat the damage it is almost certainly causing. As readers of my Substack know, I now believe that COVID, Long COVID and what I call Spike Protein Progeria Disease (SPPD) is caused be the Spike Protein’s ability to induce mistranslations of proteins. Please see my previous posts for an explanation of the mechanism and supporting papers.
I believe a very powerful therapeutic against this mistranslation damage is Nicotinamide Riboside. So, first, what is Nicotinamide Riboside?
Nicotinamide riboside (NR) is an additional salvageable NAD+ precursor with a two-step or three-step pathway to form NAD+. Nicotinamide riboside (NR) has recently become one of the most studied nicotinamide adenine dinucleotide (NAD+) precursors, due to its numerous potential health benefits mediated via elevated NAD+ content in the body. NAD+ is an essential coenzyme that plays important roles in various metabolic pathways and increasing its overall content has been confirmed as a valuable strategy for treating a wide variety of pathophysiological conditions. Accumulating evidence on NRs’ health benefits has validated its efficiency across numerous animal and human studies for the treatment of a number of cardiovascular, neurodegenerative, and metabolic disorders.
Nicotinamide Riboside—The Current State of Research and Therapeutic Uses
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352172/
Why I believe this compound is important in the treatment of COVID, Long COVID and SPPD, is because it addresses the very kind of damage I believe the evidence shows the Spike Protein is causing.
Instead, compounds and interventions that have the capacity to reduce DNA damage accumulation at its core are the ones that will be identified using DNA repair-deficient models. This is likely reflected in the positive effects noted by two different NAD+ precursors, NA and NR. NAD+ has shown to decline with age and its supplementation has shown promising results both in normal and accelerated aging and in (segmental) aging disorders of post-mitotic tissues (Xie et al., 2020; Imai and Guarente, 2014; Scheibye-Knudsen et al., 2014; Abdellatif et al., 2021a; Maynard et al., 2015). NAD+ is central for cellular processes such as metabolism and mitochondrial function, but also acts as a substrate for cAPD-ribose synthases (CD38), sirtuin deacetylases and poly-ADP-ribose polymerases (PARPs), a DNA damage sensors which is critical to various DNA repair processes and a trigger for apoptosis (Xie et al., 2020). Thus, it remains a possibility, that even though the mice are genetically deficient in TCR that NAD+ supplementation boosts complimentary alternative PARP-mediated DNA repair processes or influences signals triggered by DNA damage.
NA and NR follow different pathways of being synthesized into NAD, and their oral bioavailability is likely to differ (Trammell et al., 2016; Mehmel et al., 2020). Furthermore, the subcellular uptake of the distinct NAD+ precursors across tissues might differ with flux analysis showing, e.g., that NA is unlikely to be used in the brain but rather in spleen, intestine, pancreas and liver (Liu et al., 2018; Xie et al., 2020; Hikosaka et al., 2021). This could explain the difference we noted in our results; whereas NA specifically delayed the onset of imbalance, NR significantly extended lifespan, beyond the maximum age reached by any of the other drugs tested (Figure 4).
Together, our results show that progeroid mouse models can be used as efficient, economical, and relatively rapid screening platforms for validation of drugs or interventions that target DNA damage accumulation and/or benefit insufficient DNA repair.
The use of progeroid DNA repair-deficient mice for assessing anti-aging compounds, illustrating the benefits of nicotinamide riboside
https://www.frontiersin.org/articles/10.3389/fragi.2022.1005322/full
So, I believe trials should be initiated immediately to determine the efficacy of Nicotinamide Riboside to treat the apparent translational errors which the Spike Protein of SARS-CoV-2 is inducing.
https://wmcresearch.substack.com/p/friday-hope-nicotinamide-riboside
https://en.wikipedia.org/wiki/Nicotine
not even close.
His parents…
Mother Nassau County Jail guard and fmr. court reporter Long Island NY
Father Child and Family Court Nassau County Long Island NY
totally not mediums for intel trafficking and inmate surveillance. /s
No corruption or Mafia activity in Nassau County NY either. /s
Bonus: mother retired in Sherriff Scott Israel's Broward County Fla.
Member of Congress reads AI-generated speech on House floor
https://apnews.com/article/technology-science-oddities-israel-massachusetts-11b4dc6e42afd2d68be28dedf86fd25a
BOSTON (AP) — When U.S. Rep. Jake Auchincloss decided to deliver a speech on a bill that would create a U.S.-Israel artificial intelligence center, he opted to let the AI do the talking.
The brief two-paragragh speech read by the Massachusetts Democrat on the floor of the U.S. House on Wednesday was generated by the online AI chatbot ChatGPT. His staff said they believe it’s the first time an AI-written speech was read in Congress.
Auchincloss said he prompted the system in part to “write 100 words to deliver on the floor of the House of Representatives” about the legislation. Auchincloss said he had to refine the prompt several times to produce the text he ultimately read.
The bill, which Auchincloss is refiling, would establish a joint U.S.-Israel AI Center in the United States to serve as a hub for AI research and development in the public, private and education sectors.
Auchincloss said part of the decision to read a ChatGPT-generated text was to help spur debate on AI and the challenges and opportunities created by it. He said he doesn’t want to see a repeat of the advent of social media, which started small and ballooned faster than Congress could react.
“I’m the youngest parent in the Democratic caucus, AI is going to be part of my life and it could be a general purpose technology for my children,” said Auchincloss, 34.
The release of ChatGPT and other AI programs available on the internet is already posing a challenge for teachers who must now grapple with the possibility of students handing in AI-generated essays.
Researchers also worry AI chatbots could help turbocharge efforts to spread misinformation and propaganda.
OpenAI, the nonprofit that created ChatGPT, has acknowledged on its website that ChatGPT “can occasionally produce incorrect answers” and that its responses will sometimes be misleading as a result of how it learns. It recommends users check whether responses are accurate or not,
The text generated from Auchincloss’s prompt includes sentences like: “We must collaborate with international partners like the Israeli government to ensure that the United States maintains a leadership role in AI research and development and responsibly explores the many possibilities evolving technologies provide.”
“There were probably about a dozen of my colleagues on the floor. I bet none of them knew it was written by a computer,” he said.
Lawmakers and others shouldn’t be reflexively hostile to the new technology, but also shouldn’t wait too long before drafting policies or new laws to help regulate it, Auchincloss said.
In particular, he argued that the country needs a “public counterweight” to the big tech firms that would help guarantee that smaller developers and universities have access to the same cloud computing, cutting edge algorithms and raw data as larger companies.
Evidence illustrates that writing, proofing, editing, research, marketing, advertising, coding, media and entertainment, teaching, librarians, sales, governance, investments, currencies, logistics, supply chain, procurement, justice, energy distribution, resource allocation and management, and warfare C&C are all currently being permanently displaced by AI.
https://www.geni.com/people/Lillian-Hannity/6000000065115186847
same hannity. that is his momma. anon is related to her former boss at Nassau Cty Jail.
https://en.wikipedia.org/wiki/Sean_Hannity
Warp Speed was a MIL OP.
https://www.defense.gov/News/News-Stories/Article/Article/2188680/army-general-to-co-lead-operation-warp-speed-for-covid-19-vaccine/
DOD/DARPA was the 'only option' capable of doing this. That is how this anon reads it.
Removing the Viral Threat: Two Months to Stop Pandemic X from Taking Hold(2017)
DARPA aims to develop an integrated end-to-end platform that uses nucleic acid sequences to halt the spread of viral infections in sixty days or less
OUTREACH@DARPA.MIL
2/6/2017
Over the past several years, DARPA-funded researchers have pioneered RNA vaccine technology, a medical countermeasure against infectious diseases that uses coded genetic constructs to stimulate production of viral proteins in the body, which in turn can trigger a protective antibody response. As a follow-on effort, DARPA funded research into genetic constructs that can directly stimulate production of antibodies in the body.1,2 DARPA is now launching the Pandemic Prevention Platform (P3) program, aimed at developing that foundational work into an entire system capable of halting the spread of any viral disease outbreak before it can escalate to pandemic status. Such a capability would offer a stark contrast to the state of the art for developing and deploying traditional vaccines—a process that does not deliver treatments to patients until months, years, or even decades after a viral threat emerges.
“DARPA’s goal is to create a technology platform that can place a protective treatment into health providers’ hands within 60 days of a pathogen being identified, and have that treatment induce protection in patients within three days of administration. We need to be able to move at this speed considering how quickly outbreaks can get out of control,” said Matt Hepburn, the P3 Program Manager. “The technology needs to work on any viral disease, whether it’s one humans have faced before or not.”
Recent outbreaks of viral infectious diseases such as Zika, H1N1 influenza, and Ebola have cast into sharp relief the inability of the global health system to rapidly contain the spread of a disease using existing tools and procedures. State-of-the-art medical countermeasures typically take many months or even years to develop, produce, distribute, and administer. These solutions often arrive too late—if at all—and in quantities too small to respond to emerging threats. In contrast, the envisioned P3 platform would cut response time to weeks and stay within the window of relevance for containing an outbreak.
Key to this undertaking are nucleic-acid-based technologies—those that are centered on DNA and RNA—including some developed under DARPA’s Autonomous Diagnostics to Enable Prevention and Therapeutics (ADEPT) program. Using these tools, scientists can identify protective antibodies from recovering patients and then, through a biological version of reverse engineering, manufacture genetic constructs that, when delivered, can instruct an individual’s body to produce similar protective antibodies. Significant quantities of these nucleic acid “blueprints” can be rapidly manufactured compared to state-of-the-art antibody production methods.
What is required now are breakthroughs in three other technology areas to bridge those past DARPA achievements and overcome the remaining bottlenecks that hinder rapid response to pandemic threats. The P3 program will pursue innovations in those three areas:
Growing virus needed to support evaluation of therapies in laboratory tests;
Subjecting antibodies to rapid rounds of evolution outside of the body to increase their potency beyond that of even the most effective antibodies obtained from infected patients; and
Developing means of efficiently delivering nucleic-acid-based protective treatments, since the technologies used to administer conventional vaccines do not readily translate.
Achieving and integrating breakthroughs in all of these areas will require choreographed cooperation among researchers and engineers specializing in such areas as immunology, microbiology, virology, medical infectious diseases, molecular biology, and medical countermeasure product development and manufacturing.
DARPA-funded teams will be required to demonstrate their integrated platforms in five simulations during the planned four-year program; they will initially test their platforms using pathogens of their choice, but ultimately they will test using DARPA-selected pathogens, including two demonstrations in which the identity of the pathogen will remain opaque to the teams until the 60-day clock starts. To ensure the developed platforms can produce a quality product with a viable pathway for regulatory review, each team will be required to complete a Phase I clinical safety trial before the end of the program.
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A benefit of the nucleic-acid-based approach to limiting the spread of infection is that the genetic constructs introduced to the body would be processed quickly and would not integrate into an individual’s genome. Similarly, the antibodies produced in response to the treatment would only be present in the body for weeks to months. This is consistent with DARPA's intent with P3, which is to safely deliver transient immunity to a virus, halting the spread of disease by creating a firewall.
“Our country asks our military Service members to deploy globally and provide humanitarian assistance in all manner of high-risk environments. We owe it to them to develop the best protections possible,” said Hepburn, a U.S. Army physician who previously served as Director of Medical Preparedness on the White House National Security Staff. “If we’re successful, DARPA could take viral infectious disease outbreaks off the table as a threat to U.S. troops and as a driver of global instability.”
To further clarify the P3 program vision, answer questions from potential proposers, and facilitate teaming, DARPA is hosting two identical Proposers Days. The first will be at the Crown Plaza Tysons Corner McLean Hotel in McLean, Va., on February 22, 2017, and the second at the Doubletree by Hilton Hotel San Diego Downtown in San Diego on March 2, 2017. For registration information, visit: http://www.cvent.com/d/9vqy52.
Full details of the P3 program are included in a Broad Agency Announcement, available at: http://go.usa.gov/x9FbG. Proposal abstracts are due by 12:00 PM ET on March 13, 2017. Full proposals are due by 5:00 PM ET on May 1, 2017.
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DARPA-funded researchers have pioneered RNA vaccine technology