If you’re a fan of conspiracies, you’re going to love this show, where Mel K interviews Japan-based Canadian journalist, Benjamin Fulford. Fulford says it has been forensically proven – that he could prove it in a court of law – that there is a group of about a million people who he calls the “Khazarian Mafia” who are also known as the “Sabbatean Frankists”. He says this group came to the conclusion that it was … continued:
Category Archives: reality
Pharmacist Quits Job and Spill the Beans – CVS Pharmacy Pays $6,500/Week for Giving Vaccines
She couldn’t wait for the first load of vaccines to arrive at their store so she could read the scientific recipe data sheet that always accompanied vaccines.
The covid “vaccine” information had only one thing printed 3 times:
“Left intentionally blank”
There’s MUCH more!
Download the video:
https://dlsharefile.com/file/OGI4OTdlZjkt
Source: Pharmacist Quits Job and Spill the Beans – CVS Pharmacy Pays $6,500/Week for Giving Vaccines
Fear Is Contagious and Used To Control You – by Dr. Joseph Mercola | Mercola.com | LewRockwell.com
Governments are using fear to control and manipulate their citizens. That has now been admitted by members of the Scientific Pandemic Influenza Group on Behavior (SPI-B), a subcommittee that advises the Scientific Advisory Group for Emergencies (SAGE) in the U.K. And they should know, because they advocated for it, and now say it was a regrettable mistake. As reported by The Telegraph, May 14, 2021:1 “Scientists on a committee that encouraged the use of fear to control people’s behavior during the COVID pandemic have admitted its work was ‘unethical’ and ‘totalitarian.’ Members of the Scientific Pandemic Influenza Group on Behavior … Continue reading →
Source: Fear Is Contagious and Used To Control You – LewRockwell
Covid-19 vaccines: In the rush for regulatory approval, do we need more data? | Peter Doshi, senior editor | bmj.com
BMJ is a global healthcare knowledge provider with a vision for a healthier world. We share knowledge and expertise to improve healthcare outcomes.
BMJ 2021; 373 doi: https://doi.org/10.1136/bmj.n1244 (Published 18 May 2021) Cite this as: BMJ 2021;373:n1244
Read our latest coverage of the coronavirus pandemic
In April 2021, Pfizer and Moderna announced efficacy results at the six month mark from the phase III trials of their respective covid-19 vaccines.12
Pfizer CEO Albert Bourla said the company’s data “confirm the favorable efficacy and safety profile of our vaccine and position us to submit a Biologics License Application to the US FDA [Food and Drug Administration].”1 And on 7 May it formally initiated that application which, if successful, will earn the Pfizer-BioNTech product, BNT162b2, the distinction of becoming the first covid-19 vaccine approved by the FDA.
Because lest we forget, all covid-19 vaccines currently in use in the US are available under emergency access only.
(The situation is similar in Europe, where four covid-19 vaccines have been granted “conditional marketing authorisations,” a fast track mechanism that can be used in emergencies. These can be converted into standard “marketing authorisations” pending positive data after authorisation, but this has not yet happened for any covid-19 vaccine being administered.)
As hundreds of millions of people around the world get vaccinated, it may seem like wordsmithing to highlight the fact that none of the covid-19 vaccines in use are actually “approved.” Through an emergency access mechanism known as Emergency Use Authorisation (EUA), the products being rolled out still technically remain “investigational.”3 Factsheets distributed to vaccinees are clear: “There is no FDA approved vaccine to prevent covid-19.”4
The approval-authorisation distinction is often misunderstood by the media,5 even in the scientific press. But it was the focus of much discussion back in September 2020. With large phase III trials by Pfizer and Moderna well under way, and the November US presidential election looming, many worried about political pressure resulting in the rollout of an unsafe or ineffective vaccine.6
The FDA had already come under fire, accused of bending to the White House in granting EUAs for two covid-19 treatments, hydroxychloroquine and convalescent plasma. But those fears largely dissipated when the FDA published a guidance document in early October outlining its expectations for the EUA. According to the document, at least half of a trial’s participants would need to be followed for at least two months.7 This alone made it all but certain no vaccine could cross the line before the election.
The FDA also said it would want a vaccine at least 50% effective (with a confidence interval reaching no lower than 30%) against a primary endpoint of preventing SARS-CoV-2 infection or covid-19 disease of any severity8—parameters it had previously defined as necessary for approval. Even for non-clinical parameters, like manufacturing quality, the FDA characterised its expectations for the EUA as “very similar” to those for approval.3
Six months: enough?
One key difference between EUA and approval (also called “licensure,” and which for vaccines is known as a BLA (Biologics License Application)) was the expected length of follow-up of trial participants. Unlike its clear articulation of two months for an EUA, the FDA has not committed to a clear minimum for approval.
Cody Meissner, a professor of paediatrics at Tufts University and member of the FDA’s advisory committee, was curious. “Is it possible to predict or estimate when conditions of safety and efficacy might be satisfied for BLA?” Meissner asked at the agency’s 10 December meeting which had been convened to consider the FDA’s first emergency authorisation for the Pfizer vaccine.
The FDA’s Doran Fink responded: “I couldn’t predict, but I will say that we typically ask for at least six months of follow-up in a substantial number of clinical trial participants to constitute a safety database that would support licensure.”
An approval based on six months of data would represent one of the fastest for a novel vaccine in FDA history. Among the six “first in disease” vaccines approved by the FDA since 2006, pre-licensure pivotal trials were a median of 23 months in duration, according to a recent analysis.9
Six months also seems substantially shorter than previously conceptualised expectations. A World Health Organization expert group on covid-19 vaccines (which included FDA regulators) in August 2020 called for follow-up “until at least month 12, or until an effective vaccine is deployed locally.”10 Another group, composed of industry and academic authors, similarly wrote in October 2020: “we recommend longer term follow-up of all participants … for at least a year after randomisation.”11
On paper, the phase III studies by Pfizer, Moderna, and Janssen are all of two years’ duration. But the FDA’s official position on minimum follow-up before licensure is unclear at best.
In its formal guidance last June, the agency said that for licensure applications, it wanted participants followed for covid-19 outcomes for “as long as feasible, ideally at least one to two years”12 after the first injection. But the same document states that safety assessments for “serious and other medically attended adverse events” should be studied “for at least six months after completion of all study vaccinations. Longer safety monitoring may be warranted for certain vaccine platforms.”
Asked to clarify whether its guidance is asking for follow-up of at least six months or one year, a spokesperson told The BMJ: “We do not have any further information beyond what is in the guidance document.”
Unblinded and without a control group—what about safety?
Duration of protection is not the only question that longer, placebo controlled trials can address. They also address vaccine safety.
Continued at Source:
You Have More Power Than You Think | David Icke
You Have More Power Than You Think | David Icke # DavidIcke # DavidIckevideos #motivation 🔈 SPEAKER: David Icke More Here – ►►The Most Important Question | Alan Watts https://youtu.be/2pteZfbssgA ►►David Icke | We Are All In Trouble https://youtu.be/VMt7D1DQufQ ►►Most People See It Once It’s Too Late | Alan Watts on Individuality https://youtu.be/e9-9xlle8Q4 ►►David Icke | The Truth That Most People Refuse To See.. https://youtu.be/7MHfK6n2KFE ►►If You Use Social Media YOU D BETTER SEE THIS! | Jordan Peterson https://youtu.be/B-UB9dVq7gw ►►We Are Being Set Up! https://youtu.be/TmnArTkOoSU ►►These Events Will Change Everything https://youtu.be/0yMfqgGDghE Topics Are – meditation becoming supernatural, pineal gland meditation, breathing technique, sleep meditation, heal your body with your mind, walking meditation, blessing of the energy centres,
US Senate passes bill to give billions of dollars in funding for human-animal hybrid experiments | LifeSiteNews.com
We shouldn’t need to clarify in law that creating animal-human hybrids or chimeras is ethically unthinkable, but sadly the need for that very clear distinction has arrived, said Senator James Lankford.
Mon Jun 14, 2021
WASHINGTON, D.C. June 14, 2021 (LifeSiteNews) – The U.S. Senate has passed a bill which will allocate billions of dollars to the National Institutes of Health (NIH), with some of the funds expected to go toward a disturbing form of research whereby tissue from aborted babies is spliced with animal cells to create mixed-species organisms called “chimeras.”
Introduced by Senate Majority Leader Chuck Schumer (D-New York), the U.S. Innovation and Competition Act (USICA), also called the “Endless Frontier Act,” was passed by the Senate in a 68-32 vote June 9.
Supposed to address growing Chinese technological competition by increasing investment in American innovation in science and technology to the tune of $250 billion, the bill had been hotly debated on the Senate floor for weeks, with over 600 amendments being proposed before last week’s vote.
Although the measure passed with significant bipartisan support, it had drawn fire from Senate Republicans concerned about the possible ethical implications of some of the bill’s intended spending.
One of their concerns had to do with the bill’s proposed funding for the National Institutes of Health, which has long considered lifting its moratorium on conducting chimeric experiments pending new guidelines from the International Society for Stem Cell Research (ISSCR).
Continued on Source: US Senate passes bill to give billions of dollars in funding for human-animal hybrid experiments
The Nuremberg Code ( 1947) | THERE IS NO PANDEMIC | DrCharlieWard.com
Sedona Method Letting Go The Greatest Secret with Rhonda Byrne and Hale Dwoskin
VLOG 223: WE ARE MAKING PROGRESS IN TRANSFIGURING OUR EARTHLY BODIES | Patricia Cota Robles
Dr. Joe Dispenza ON: Unlocking the Unlimited Power of Your Mind & Healing Yourself Through Thought | Jay Shetty Podcast
Dr. Joe Dispenza joins Jay Shetty to talk about how our thoughts and emotions can affect our physical body, the unconscious process of making your feelings become the means of thinking, and reaching an awareness of the possibilities you haven’t thought before. Dr Joe holds a Bachelor of Science degree and is a Doctor of Chiropractic. His post graduate training includes the fields of neuroscience and neuroplasticity, quantitative electroencephalogram (QEEG) measurements, epigenetics, mind-body medicine, and brain/heart coherence.
(Easier to read aligned on YouTube: https://youtu.be/J0AibK15MwM )
What We Discuss with Dr. Joe: 00:00 Intro 01:55 What’s the biggest difficulty or challenge you’ve had to overcome in the past 12 months? 04:57 Challenging thoughts we’ve developed that affects how we feel 07:34 The Familiar Past, our feelings become the means of thinking 12:33 Overcoming your old personality to create the energy to heal 18:24 In the unknown, you learn how to be comfortable with the unknown 23:27 Processing problems productively and effectively through thoughts 27:50 Not reacting emotionally is going to change the energy of how you address a situation 33:17 The fear has to be addressed if you want to be healed 37:54 Why is our memory for pain stronger than our memory of success or joy? 43:19 Your experience produces a feeling that is not chemical 48:25 What disconnects us from our awakening and connection to the divine 54:36 Deducing the energy frequency of the people you meet 58:11 The heart is the middle path, it’s a union of polarity 01:08:47 People are the example of truth, we take care of one another and we heal together 01:14:13 The purpose of life is to figure out its purpose 01:17:02 Dr. Joe on Final Five Text me: 310-997-4177 — Subscribe and be a part of the movement to make wisdom go viral: http://bit.ly/2n6hiQP- — Join the conversation by commenting below. — Enroll in Genius Coaching to improve your life, deepen your relationships and find happiness every day: https://pages.jayshetty.me/genius/ — Check Out My New Book, Think Like a Monk: https://thinklikeamonkbook.com/ — Jay Shetty is a storyteller, podcaster, and former monk who wants to make wisdom go viral. He loves taking his own life experiences, lessons from his time as a monk, and truths he has learned to make others’ lives better. — Follow me on Social Media: LinkedIn: https://www.linkedin.com/in/shettyjay… Facebook: https://www.facebook.com/JayShettyIW/ Twitter: https://twitter.com/jayshettyiw Instagram: https://www.instagram.com/jayshetty Pinterest: https://www.pinterest.co.uk/jayshetty… Sign up for my Viral Wisdom Newsletter: https://jayshetty.me/email





