Available on my Bitchute channel.
What dystopian world are we living in? You just can’t make this stuff up! The mRNA gene-altering medical device, that has never been used on humans before, was only was under stage 3 trials for 3 months in humans with placebo then that continued in the global population since. Over 20,000 have died from the Pfizer shots in the US, Europe and UK as recorded by their government reporting systems, which are known to be under reported by at least 10 times. Now the death shot has been given full FDA “approval” for humans 16 years and older. See below for explanation.
Welcome to the future. Gene altered transhumans with graphene-oxide based biocircuitry is the plan for those few who survive the death shots.
The totally corrupt and captured US FDA has explained in their own document this way.
There you read the following:
Audience: Individuals Performing COVID-19 Testing
Level: Laboratory Alert
After December 31, 2021, CDC will withdraw the request to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) of the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2 only. CDC is providing this advance notice for clinical laboratories to have adequate time to select and implement one of the many FDA-authorized alternatives.
In preparation for this change, CDC recommends clinical laboratories and testing sites that have been using the CDC 2019-nCoV RT-PCR assay select and begin their transition to another FDA-authorized COVID-19 test. CDC encourages laboratories to consider adoption of a multiplexed method that can facilitate detection and differentiation of SARS-CoV-2 and influenza viruses. Such assays can facilitate continued testing for both influenza and SARS-CoV-2 and can save both time and resources as we head into influenza season. Laboratories and testing sites should validate and verify their selected assay within their facility before beginning clinical testing.
But what both Dr. Vivek Murthy and Press Secretary Jen Psaki neglect to say is that the biggest misinformation is coming from the CDC, FDA, and NIH. Those organizations do not want you to know how many people have been killed or permanently disabled by the COVID vaccines. And they want you to believe that early treatments don’t work.
They don’t want you to know that their own data shows that for the alpha variant, vaccination only makes sense if you are over 30 years old and for the delta variant, because it is nearly 7 times less deadly, vaccination makes no sense at all: for all ages, it will kill more people than it will save. Finally, early treatments are the superior alternative: they are proven in practice to have a higher risk reduction and better safety profile than any of the current vaccines. The NIH and WHO are deliberately suppressing this information in order to push the “mass vaccination is the only option” false narrative (breaking with 70 years of established science).
Furthermore, the latest statistics show that vaccination could be making people more susceptible of dying from COVID, not less susceptible like everyone assumes. Is this due to ADE (antibody dependent enhancement)? There is a simple way to find out. We’ve asked the FDA why they aren’t doing autopsies to confirm or deny that this is happening, but they have not answered. This should be baffling to anyone in the medical community how we are not gathering this critical data.
Australia (TGA) has a voluntary reporting system for adverse drug and vaccine reactions. See report here for those adverse reactions up to 27 June 2021. They report 4.6 adverse reactions per 1000 which translates to 0.46% of the total number of doses administered. Also they list 335 deaths up to this time.
But since this is voluntary reporting system, and also we have heard how people are discouraged from filing reports, does the TGA have any real idea of what the truth really is? What percentage are actually reported>
Reposted from ALLIANCE FOR HUMAN RESEARCH PROTECTION
January 14, 2021
Below, Meryl Nass, MD explains what is known and what remains unknown about the experimental Covid-19 vaccines. Her post was prompted by the fact that her state of Maine requires its Emergency Medical Teams, who refuse the experimental vaccine, to sign a “Declination Form” that contains False and Misleading statements.
Luckily, there are several FDA-licensed drugs as well as vitamins/supplements that are effective against Covid infection. These medications and supplements are safe, and have been used for many decades. Read: How A False Hydroxychloroquine Narrative Was Created