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| Madalina Vasiliu/The Epoch Times |
Think back to those grim days of mid-March 2020. Many things didn't make sense. There were screams about a new virus but no tests available for anyone to find out if we had the dreaded disease or not. The main question in everyone’s mind was, “How can I find out if I have this strange new bug?”
Hold on just a moment there. If there were no tests, how do we know that there was a reason to panic? If there were only a handful of positive tests, how do we know for sure that the virus wasn’t here and spreading months earlier? Maybe what they were calling COVID-19 was here for a year or more.
Was there really any way to know? Sure, we could have done seroprevalence tests on the population, but there were none underway. The one that came out earliest, in May 2020, showed that exposure had already happened by March, a fact which completely undermines the entire cockamamie policy response. The study was brutally attacked.
Why precisely was it mid-March 2020 when all official institutions, including media, not just in the United States but all over the world, decided suddenly to freak out? Why not in January 2020? Why at all?
Indeed, it wasn't even clear what the point of the lockdowns was. Were we trying to make the virus go away through brute force? Early on, then-Director of the National Institute of Allergy and Infectious Diseases Dr. Anthony Fauci even told The Washington Post that the virus would be defeated by social distancing alone.
What precisely would be the point of delaying infection and spread by two weeks, then another two weeks, and so on? There are endless questions. How did we know how many ventilators were going to be needed and where? And ventilation itself is a strange approach in any case, since it's so deeply damaging and even deadly.
There was zero evidence in mid-March that this virus was potentially fatal for working-age people, and even among healthy elderly people, the survival rate was extremely high.
Another strange fact of those days was that they kept screaming that there was no treatment. Well, are we sure of that? No one in official channels was looking for treatments. How do we find treatments? By talking to experienced doctors who treat patients. But every time one of them spoke out, they were quickly and brutally shouted down and denounced. --->READ MORE HERE
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| Ezra Acayan/Getty Images |
The public was not made aware that COVID-19 vaccines contained enhancer DNA sequences from the SV40 virus known to cause cancer in lab animals.
Dr. Robert Malone, the inventor of mRNA and DNA vaccines, slammed health regulatory agencies for not informing people about potential plasmid DNA contamination in mRNA COVID-19 vaccines.
An Oct. 19 preprint study found billions of residual DNA fragments in mRNA COVID-19 vaccine vials. While billions of copies of spike, ori, and SV40 enhancer DNA were discovered in the Pfizer vaccine vials, Moderna vials were found to contain copies of ori and spike DNA. The SV40 virus is a DNA virus known to cause cancer in lab animals.
Talking about the study in a Nov. 11 Substack post, Dr. Malone said that plasmid DNA contamination in the vaccines is a “proven fact” that has been “acknowledged by the US FDA, Health Canada, and the European Medicines Agency.”
“In yet another clear breach of informed consent and labeling requirements, this was not previously disclosed to physicians, public health officials, or patients,” he wrote.
For instance, the FDA’s labeling guidelines require that vaccine labels must contain a description of “serious adverse reactions, potential safety hazards, steps that should be taken in the occurrence of a serious adverse reaction and potential safety hazard, and limitations in use imposed by them.”
Pfizer and Moderna COVID-19 mRNA vaccines “are contaminated with plasmid DNA fragments which have not been removed during the current manufacturing processes,” the doctor wrote. A plasmid is a strand of circular DNA that is common to bacteria and specific parasites.
Dr. Malone said that prior FDA guidance on DNA vaccine technology pointed to the presence of “highly active regulatory sequences as being of particular concern due to potential insertional mutagenesis (integration).”
The FDA’s 2009 “Guidance on Prophylactic DNA Vaccines: Analysis and Recommendations” states that concerns about plasmid DNA potentially integrating into the genome of the vaccine recipient and increasing the likelihood of issues like “malignant transformation, genomic instability, or cell growth dysregulation” were raised when DNA vaccines were initially introduced for clinical use.
It stated that a “tiny fraction” of the plasmids are expected to “integrate into the host genome, regardless of the method of delivery.” --->READ MORE HEREFollow links below to relevant/related stories and resources:
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