Facebook Insider Morgan Kahmann joins Tucker Carlson to discuss leaked ‘Vaccine Hesitancy’ documents | Fox News

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Learn About Our New Lawsuit [against the Dept. of Health & Human Services, FDA, CDC, and others concerning use of vaccines in children under the age of 16]! | Dr. Pam Popper | MakeAmericansFreeAgain.com

Source: Learn About Our New Lawsuit!

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Michael Jaco Discusses Trump, Deepstate, Vaccines And Currencies With Nicholas Veniamin

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Dr. Rand Paul Stops Gain-of-Function Research Funding in China | www.paul.senate.gov

FOR IMMEDIATE RELEASE:
May 25, 2021
Contact: Press@paul.senate.gov, 202-224-4343

WASHINGTON, D.C. – Today, the U.S. Senate passed U.S. Senator Rand Paul’s amendment that would permanently ban all funding of gain-of-function research in China. This is following much back-and-forth with Dr. Fauci, and continually defending against the use of American taxpayer dollars in funding gain-of-function research, which aims to enhance the infectiousness or severity of a virus. The amendment is co-sponsored by U.S. Senator Ron Johnson (R-WI), U.S. Senator Tommy Tuberville (R-AL), Dr. Roger Marshall (R-KS), U.S. Senator Mike Braun (R-IN), and U.S. Senator Thom Tillis (R-NC).

“We don’t know whether the pandemic started in a lab in Wuhan or evolved naturally,” said Dr. Paul. “While many still deny funding gain-of-function research in Wuhan, experts believe otherwise. The passage of my amendment ensures that this never happens in the future. No taxpayer money should have ever been used to fund gain-of-function research in Wuhan, and now we permanently have put it to a stop.”

Senate Amendment 2003 bans the National Institutes of Health and any other U.S. agency from funding any gain-of-function research in China.

The amendment defines gain-of-function research as “any research project that may be reasonably anticipated to confer attributes to influenza, MERS, or SARS viruses such that the virus would have enhanced pathogenicity or transmissibility in mammals.” This is the same definition the NIH used when implementing a funding moratorium on gain-of-function research in 2014-2017.

The origin of the COVID-19 virus is unknown. It has yet to be determined if the outbreak began through contact with infected animals or due to a laboratory accident at the Wuhan Institute of Virology in China. But this pandemic, and the questions of its origin, has exposed the inherent risk of gain-of-function research and never again will taxpayer dollars fund this type of research in China.

You can read S. 2003 in its entirety HERE.

BACKGROUND:

During a Senate HELP hearing on May 11, Dr. Paul specifically asked Dr. Fauci about the funding of gain-of-function research at the Wuhan Institute of Virology, and the potential link between the COVID-19 outbreak and the lab itself. Gain-of-function research essentially involves juicing up naturally-occurring animal viruses to infect humans.

For years, Dr. Ralph Baric, a virologist in the U.S. has been collaborating with Dr. Shi Zhengli of the Wuhan Virology Institute, sharing his discoveries about how to create super viruses. During their research, Dr. Baric and Dr. Shi worked together to insert bat virus spike protein into the backbone of the deadly SARS virus and then used the man-made super virus to infect human airway cells.

Much of the research they were doing was funded through Dr. Fauci’s NIH and NIAID.

When Dr. Paul asked Dr. Fauci whether he supports the NIH funding of the lab in Wuhan, Dr. Fauci, a strong supporter and ardent advocate of gain-of-function research, claimed that the NIH “has not ever and does not now fund gain-of-function research in the Wuhan Institute of Virology.”

Despite Dr. Fauci’s previous denials, there is ample evidence and backing by the scientific community that the NIH and the NIAID, under his direction, funded gain-of-function research at the Wuhan Institute of Virology. A multitude of scientists have reviewed this research and said it meets the definition for gain-of-function. Many of these scientists have also discussed the inherent dangers of conducting gain-of-function research and the risks it poses to the human population.
###

Dr. Lawrence Palevsky on spike protein shedding | America’s Frontline Doctors

https://www.youtube.com/watch?v=TcAXxeWK-Ew

Dr. Lawrence Palevsky spoke in an interview about the mechanics of spike protein shedding: “When studies are done on injections that are thought to be vaccine, we sometimes need 7, 10, or even 15 years to really understand what the injection does to the body, and what it does to those around us.

“And so, there’s automatically this assumption that when the authorities say these injections are safe, that we actually have adequate data and adequate observational data to understand whether or not these injections are safe.

“The bottom line is, we don’t have enough data to understand safety.

“The other thing is that we are made to believe in the public eye that this is a vaccine against a viral infection. So the entire world is thinking that this is a vaccine to protect us against SARS Cov2 viral infection. And when you have a vaccine that’s supposed to be effective as a vaccine, you’re supposed to have antibody immunity against the SARS Cov2 virus.  And that’s never been evaluated with these injections as to whether or not we have antibody immunity to a SARS Cov2 virus.

“Instead, what we have is the genetic information of what is believed to be a piece of the SARS Cov2 virus and that piece is called the ‘spike protein’, and the technology that’s being used is a technology to make this injection that’s never been used in vaccine science or methodology before with any kind of success.

“So we are essentially taking the genetic instructions that make a synthetic spike protein believed to be a part of the SARS Cov2 virus, and we’re giving those sets of instructions into the body and asking the human body to take the genetic instructions of that spike protein and make more of it in our own machinery.

“And so, this messenger RNA technology, which is what it’s called, is delivering the genetic instruction for us to make the spike protein. And the problem is that no study has ever been done to test its safety, but also no study is been done to test whether we turn on the production of that spike protein and ever turn it off.

“And so, spike protein in the naturally occurring SARS CoV2 viral infection has been shown to cause brain inflammation and neurological damage, heart attacks, lung disease, liver disease, kidney disease, and interacting with the male and female reproductive systems, along with affecting blood binding to oxygen and blood clotting.

“And so, we know that the natural disease of SARS CoV2, because of the effects of the spike protein, is making people sick with all of these kinds of systemic illnesses. And so now we’re taking that spike protein genetic instructions, and we’re asking our bodies to make more of that spike protein. And so by making more of that spike protein, we are essentially creating the symptoms and the illness of COVID-19 by giving people the potential to have brain damage and neurological damage, lung disease, liver disease, kidney disease, heart attacks, strokes, blood clotting issues, and impairments to male and female reproductive systems.

“And there’s no study to show whether when the body starts manufacturing the synthetic spike protein – whether or not we ever turn off the production of that spike protein.

“And so that spike protein is known to be pretty damaging to the human tissue. And so, we know that spike protein has been found in saliva, we know that it’s been found in the anus, and we have to ask the question: Is it found in the exhalation molecules that come out of our breath? Is it found in the skin when we sweat and we smell the spike proteins come out? And if so, does that impact other people with whom we come in contact?

“And so, what we’ve been seeing is a massive increase in those who’ve been given the injection of blood clotting problems, miscarriages, stillborns, infertility, stroke, heart attack, autoimmune diseases, and death, just to name a few, and that’s in those who been injected.  So certainly there should be a suspicion when you see people around the injected people who have not been injected getting the typical symptoms of COVID in addition to miscarriages, bleeding, irregular menstrual cycles; it should raise a very, very strong suspicion.

“The spike protein is, we are told, just specific to the SARS CoV2 virus, so that when your body makes the synthetic spike protein, you’re supposed to produce an antibody that’s supposed to attack the spike protein.

“Now, we don’t know if that spike protein production keeps going and going and going, and that would make the antibody production keep going and going and going as well. And the thing is, that we are finding that the genetic instructions of the spike protein are not specific just to the SARS CoV2 virus. The genetic instructions of the spike protein are also similar to, or the same as, many proteins that exist in the body itself.

“And so therefore, if we’re going to produce an antibody against the genetic instructions of the spike protein, those antibodies are going to find every bit of protein tissue around the body that matches the genetic instructions of the spike protein, and that antibody to the spike protein genetic instructions is going to produce an attack on any of the proteins and tissues in the body that are similar or the same to the genetic instructions of the spike protein. So that’s why you’ll see autoimmune diseases.” Continued on Source:

https://www.americasfrontlinedoctors.org/frontline-news/can-vaccinated-people-make-the-unvaccinated-sick-watch-dr-palevsky-explain

Visit Dr. Palevsky’s website for more information:  https://www.northportwellnesscenter.com/practitioner/lawrence-palevsky/videos

The Forbidden COVID-19 Chronicles | Why Many People Are Not Getting a COVID Vaccine: Part V | Pamela A. Popper, President, Wellness Forum Health

According to an article published in the British Medical Journal in October 2020, the COVID-19 vaccine trials were not designed to determine if the vaccines were safe or effective.[1] This was a problem since the primary reason for getting any vaccine should be because it has been proven to be safe and to prevent serious illness, hospitalization, and death.

The author, Peter Doshi, is associate editor of the journal. He begins by stating that while Anthony Fauci and the FDA assured the public that only safe and effective vaccines would be made available, this was not possible due to study design.

The phase III trials of the Moderna and Pfizer vaccines were designed to end after 150-160 “events” were reported. The definition of an event was quite liberal and could include a person with a cough and a positive lab test. Mild symptoms and a test with a very high false positive rate (see articles on this topic in the Health Briefs Library) made it easy to record the required number of events, end the trial early, and apply for Emergency Use Authorization. This might be good for drug company sales, but what about consumers?

Doshi gives the drug companies the benefit if the doubt on study design, pointing out that one of the reasons for categorizing mild symptoms and a test as an event might have been that the rate of severe illness and hospitalization due to COVID-19 was so low – only 3.4% overall. This means that even trials with tens of thousands of patients would only show a few cases of severe illness. And these trials were much smaller. Of course, a reasonable person might ask why a vaccine is needed for a disease that has a such a low rate of severe illness and hospitalization and an overall survival rate of 99.98%. But as we have learned during the last 15 months, reasonable people are not in charge of our government right now.

Doshi reports that the drug companies acknowledged the limitations of the trials. Tal Zaks, chief medical officer of Moderna, admitted that the trial could not determine whether or not the vaccine reduced hospitalizations based on its size and duration. This did not stop Moderna from reporting to the media that hospital admissions were a “key secondary endpoint.”

Zaks also admitted that the trial could not determine whether or not the vaccine reduced the risk of death from COVID, stating “Would I like to know that this prevents mortality? Sure, because I believe it does. I just don’t think it’s feasible within the timeframe [of the trial]…”

And then Zaks admitted that the trials would not even demonstrate that the vaccine would prevent transmission because a trial that would evaluate this endpoint would take too long and would be too expensive. Really? Moderna received almost a billion dollars from The Biomedical Advanced Research and Development Authority (BARDA), which is part of the Department of Health and Human Services. The taxpayers funded the development of this vaccine and Moderna is arguing that proving efficacy is too expensive.[2] Really?

But that’s not all. the federal government also committed $1.5 billion for 100 million doses of the Moderna vaccine. Americans did not get a vaccine that was safe and effective, but we did make Moderna executives rich. Stock sales that coincided with announcements of trial results totaled $100 million dollars for just three executives.[3]

in addition to providing funding, the U.S. government assisted Moderna by distributing false information about the trials. A press release from the National Institutes of Health stated that Moderna’s trial “aims to study whether the vaccine can prevent severe covid-19” and “seeks to answer if the vaccine can prevent death caused by covid-19.”

Doshi writes that most of the general public assumes that the point of the trials is to test safety and efficacy, and asks Zaks, “How do you reconcile that?”

I give Zaks credit for honesty. He replied, “Very simply…we have a bad outcome as our endpoint. It’s covid-19 disease.” In other words, NIH press releases concerning the Moderna vaccine were patently false, and the trial was a charade.

Doshi points out that issues with study design for trials of flu vaccines are not new. He reports that only two placebo-controlled trials including elderly people living in community settings have ever been conducted, and neither was designed to evaluate differences in hospital admissions or deaths. A further limitation is that increased uptake of flu vaccines has not led to a reduction in mortality from flu.

Shockingly, Peter Marks, an FDA official involved with vaccine approvals agreed, stating that flu vaccines only prevent flu in about half of the people who get them.

Perhaps most alarming is Doshi’s warning about adverse events resulting from vaccines that were rushed to market in the past – like the COVID vaccines. Examples include contaminated polio vaccines in 1955, cases of Guillain Barre as a result of flu vaccines in 1976, and narcolepsy which was a side effect of one flu vaccine in 2009.[4]

The only reason a person would agree to receive one of these vaccines is ignorance of the facts, and the government and vaccine makers are working very hard to make sure that people do not have access to factual information.


[1] Doshi P. “Will COVID vaccines save lives? Current trials aren’t designed to tell us.” BMJ 2020;371:m4037
[2] Judy Stone. The People’s Vaccine – Moderna’s Coronavirus Vaccine Was Largely Funded By Taxpayer Dollars. Forbes December 3 2020
[3] IBID
[4] Doshi P. “Will COVID vaccines save lives? Current trials aren’t designed to tell us.” BMJ 2020;371:m4037

Looking for articles from previous newsletters? The newsletters are included in the Health Briefs Online Library, accessible through www.wellnessforumhealth.com. A search engine on the site can help you to easily locate all of the articles that contain information about the topic you are researching.

IF PEOPLE GET JABBED AFTER WATCHING THIS THEY ARE BEYOND SAVING – lewrockwell.com Blog

This video addresses these concerns:

Not a vaccine

·         Is an Experimental mRNA injection

·         Rushed through Clinical Trails

·         Skipped proper safety testing

·         Long list o…

Source: IF PEOPLE GET JABBED AFTER WATCHING THIS THEY ARE BEYOND SAVING – LRC Blog

SHEDDING TRANSMISSION IS REAL! | Dr. Sherri Tenpenny

Dr. Sherri Tenpenny’s Telegram account: https://t.me/DrTenpenny

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Source: SHEDDING TRANSMISSION IS REAL! | Dr. Sherri Tenpenny

Mirror: 1,000 Lawyers And 10,000 Doctors Have Filed A Lawsuit For Violations Of The Nuremberg Code – Public Intelligence Blog | Robert David Steele | phibetaiota.net

Source: Mirror: 1,000 Lawyers And 10,000 Doctors Have Filed A Lawsuit For Violations Of The Nuremberg Code – Public Intelligence Blog

𝗔𝗯𝗼𝘂𝘁 𝗧𝗵𝗶𝘀 𝗩𝗶𝗱𝗲𝗼
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Ep. 2483b – Patriots Can Now See The Board Clearly, The First Domino Is Ready To Fall | X22 May 20, 2021

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The first domino is about to fall, this is going to be the shot heard around the world. Nothing can stop this nothing. The [DS] lost the battle before it began, we are in the exposure phase. The people are fighting back and the [DS] players are feeling the backlash. More pain is coming, timing is everything. Flynn sends a message, more is coming, Scavino shows Trump at the rallies, it’s time.

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Source: Ep. 2483b – Patriots Can Now See The Board Clearly, The First Domino Is Ready To Fall