Posted on 07/14/2021 1:15:25 PM PDT by Enlightened1
In a recorded phone call between a vaccine victim and a representative of Moderna, the rep admitted that everyone that subjects themselves to the vaccine is a participant in the trial.
He also admits long-term protective efficacy against Covid-19.
The woman on the phone call is suffering from Guillain-Barré syndrome after her first dose and recorded the conversation with this Moderna representaive.
Happy trails to you!
Haha!
Wall Street is playing word games, and you are very confused.
**News Flash** 28 days is not enough time. Trials typically last years not 28 days.
You do know the Moderna reps are reading the data Moderna provides them?
How many phases do you think exist?
What part of “non FDA approved experimental” mRNA gene therapy do you fail to understand?
Right now are the human trials, and it does not end until 2023.
it’s not vaxxers vs anti-vaxxers
it’s experimentals vs anti-experimentals...
Not sure too many folks on this thread do either.
Vegas has better odds than these vaccines.
Here’s the proposition — you ignore the facts that you are unlikely to get COVID and even more unlikely to have a severe case of COVID, then allow somebody to jab you with a vaccine that may or may not (a) offer any actual protection against COVID in present AND FUTURE forms, and (b) be free from harmful side effects that are worse than COVID itself would likely be for you.
This is sort of like saying, okay you just bought a lottery ticket, but if you pay me double what you paid for your lottery ticket, I’ll give you mine and take yours.
perhaps BIG PHARMA took out life insurance policies
on the victims of their mandatory “vaccines”.
“This mRNA technology has been in development for 20 years and deemed unsafe for humans.”
What’s your source for that claim? The University of Alabama says otherwise.
“the development of mRNA vaccines against COVID-19 is no overnight success. In fact, they have a remarkable back story stretching back decades. Without one researcher’s determination, two companies with vision, a longtime network of university labs, and decades of taxpayer funding in treatments for influenza and HIV, particularly by the United States’ National Institutes of Health, COVID-19 vaccines might still be years away. Even then, it took a massive, unprecedented investment by the U.S. government to get these shots from labs into arms faster than ever before.
“The remarkable success we have seen over the past few months in slowing the COVID-19 pandemic in the United States can be traced back to these four parallel stories and one big bet from the U.S. government.
1. mRNA vaccines: an idea more than 30 years in the making
When Katalin Karikó, Ph.D., came to the United States from Hungary in 1985, she brought with her a passionate determination to work on mRNA. Messenger RNA is fundamental to life: sets of blueprints, spelled out using four nucleotide “letters,” for building every protein in every life form on Earth. Karikó’s big idea was to produce proteins at will by injecting mRNA into cells, but her experiments did not work for a long time. Lack of success forced her to rely on one senior scientist after another to support her work, while she made only meager wages.
In 1998, Karikó partnered with Drew Weissman, M.D., Ph.D., at the University of Pennsylvania. Weissman was interested in developing an HIV vaccine based on mRNA. After many failures, Karikó and Weissman learned that natural mRNAs use small amounts of slightly modified nucleotides, in addition to the four standard nucleotides. When the scientists inserted the modified nucleotides into the mRNAs they were using in their research, they began to find that these modified mRNAs produced proteins efficiently without causing undesirable side effects. They began to publish their findings, starting in 2005. By the time the coronavirus that causes COVID-19 showed up in 2020, Karikó and Weissman were already working on an influenza vaccine based on their mRNA technology.
The last 16 months have served as a demonstration of how terrifyingly stupid the average person is.
The approval will not be based on science but will be a political approval, making it essentially worthless.
Yet they’re all more confident, aggressive and mouthy than most stupid people in the past.
More deeming. If it can be deemed unsafe, it can be deemed safe, too.
Yay!
Big lesson here is that you should always record your phone conversations. It’s legal in one party states. In two party states, it’s legal to record conversations with public officials without informing them. If you call some company and there is an announcement that your call may be recorded, that is a de facto permission for you to record them without informing them you are doing so.
If you have a company calling you to collect on a debt, whether you owe it or not, record the call because they are recording it, too. In almost every such call, they violate the laws related to “fair debt collection laws”. In some states, you can have the entire debt cancelled if they violate those statutes. That’s why if you ever tell them to never contact you again because they have violated the statute, you will never here from them again. There are also monetary penalties if they do. Easy to prove if you have a recording.
Have done it more than once when harassed for a debt I didn’t owe.
Signing a document printed in a very small font and not being given a verbal explanation is hardly “informed consent”.
Big Pharma has so much money, they are likely self-insured or have agreements with the Federal government to pay all claims.
Big Pharma has so much money, they are likely self-insured or have agreements with the Federal government to pay all claims.
Of course. Who thought differently?
Translation: Test Subjects.
I guess they didn’t read the brochures - not even sure what info they give when you go for the vaccine, does any of the info say it’s only approved for emergency use ?
A Dick Turban broken-clock moment?
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