The Department of Homeland Security has launched a new panel to tackle disinformationDisinformation Board to Tackle Russia, Migrant Smugglers
Recommended YouTube video: DHS Creates “Disinformation Governance Board” – It’s About The Empire! (Source)
Before her work advising the Ukrainian government, Jankowicz managed democracy assistance programs for Russia and Belarus at the National Democratic Institute for International Affairs. She holds an MA in Russian, Eurasian, and East European Studies from Georgetown University’s School of Foreign Service.
The National Democratic Institute for International Affairs (NDI) is one of the main components of the regime change organization National Endowment for Democracy (NED); that is, NED channels its funds through four organizations, and NDI is one of them, to “promote free, fair, transparent democratic elections but in such a way that it would assure that power went to the elites and not to the people”.WikiSpooks
Whistleblower Data They Ignored.
This is not just any doctor either. This is Doctor Peter Doshi, assistant professor of pharmaceutical health services at the University of Maryland and an associate editor at The British Medical Journal (BMJ)Doctor Crashes FDA Meeting, Sharing..
But the agency’s infrastructure was neglected for decades, like the nation’s public health system generally, and the pandemic has posed unprecedented challenges. Early on, the C.D.C. made key mistakes in testing and surveillance — for example, famously fumbling design of a diagnostic kit sent to state laboratories.
Officials were late to recommend masking, partly because agency scientists didn’t recognize quickly that the virus was airborne. In May of last year, Dr. Walensky announced that vaccinated people could take masks off indoors and outdoors; just weeks later, it became clear that vaccinated people could not only get breakthrough infections but also could transmit the virus.
In August, Dr. Walensky joined President Biden in supporting booster shots for all Americans, before scientists at the Food and Drug Administration or her own agency had reviewed the data on whether they were needed.
More recently, the highly contagious Omicron variant has led the C.D.C. to issue recommendations based on what once would have been considered insufficient evidence, amid growing public concern about how these guidelines affect the economy and education.
In December, the C.D.C. shortened the isolation period for infected Americans to five days, although it appears that many infected people can transmit the virus for longer. Over the past few weeks, some experts have criticized the agency for changing the metrics used to assess risk and determine appropriate local measures, in order to appease business and political interests.
Study shows effectiveness of pill form of remdesivir to treat COVID-19 in mice (Ralph Baric & Gilead Sciences)**
[Molnupiravir] EIDD-2801’s story starts years before the coronavirus crisis. In 2014, Painter and his colleagues at Emory University began a project funded by the Defense Threat Reduction Agency to find an antiviral compound that could fight Venezuelan equine encephalitis virus (VEEV). During the Cold War, both the US and the Soviet Union studied VEEV as a potential biological weapon. Typically transmitted through mosquito bites, VEEV causes high fevers, headaches, and sometimes encephalitis, swelling of the brain that can be deadly.
In late 2019, Painter got a contract from the National Institute of Allergy and Infectious Diseases* to move EIDD-2801 into Phase I clinical trials for influenza. The plan was to file an investigational new drug application and find a partner to help with the clinical work.
Just as the team was contemplating its next move, word of a virus spreading in Wuhan, China, was starting to make news. One of Painter’s collaborators, UNC coronavirus expert Ralph Baric**, immediately alerted him that the new pathogen was probably a coronavirus—one that EIDD-2801 could potentially combat.
Denison*** says the research team knew a coronavirus outbreak was inevitable. “Every single one of our grants, every single one of our papers predicted that this event was going to happen that’s occurring right now,” he says. “The whole goal of our drug development was to plan for this.”
*Anthony Fauci, director of NIAID.
The purpose of the RFI is described as being to help the authorities understand the effect of pandemic “misinformation” on such areas as “health decisions and outcomes, direct and indirect costs, trust in the healthcare system and providers, and healthcare worker morale and safety. It is also intended to help them ascertain its impact on “access to trusted and credible health information, particularly during a public health emergency” and on “lifesaving health decisions such as an individual’s likelihood to vaccinate, and to “prepare for and respond to future public health crises.”
The RFI, which covers a period extending from January 2020 to the present, applies to general search engines, content sharing platforms, social media platforms, e-commerce platforms, crowd-sourced platforms, and instant messaging systems, and includes “research, case studies, data sets, images, data visualizations, interviews, and personal testimonies.”
On YouTube: Dr. John Campbell goes over the Pfizer documents of adverse reactions to the jab. (More sources in description)
A fourth booster shot of either the Pfizer or Moderna vaccine could start an annual booster shot campaign, one of the people familiar with the FDA’s planning said.
I’m not buying the media’s scaremongering about the second omicron variant!
I’m behind because I haven’t really been keeping up with coronavirus news. Out of sight, out of mind! 🤷🏼♀️