This is not the kind of news many supporters of the placement of Robert F. Kennedy, Jr. in charge of the United States Department of Health and Human Services (HHS) wanted to see come out of the Food and Drug Administration (FDA) now under his purview. Reuters reported Thursday that the FDA had given full approval — an upgrade from the previous emergency use authorization — for a new version of the mRNA coronavirus “vaccine” of drug company Moderna for children from the age of six months to 11 years old who are identified as at increased risk from coronavirus.
Tag: vaccine
The first Donald Trump administration ushered in an American coronavirus crackdown that included among its putrid components “warp speed” production and distribution of experimental coronavirus “vaccine” shots, Those shots, though repeatedly touted by people in government and media as “safe and effective,” turned out to be both dangerous and ineffective. Now, Trump’s second administration appears to be taking another go-around with the dastardly project, with experimental mRNA shots again playing a major role. This time the excuse is bird flu.
Last week, I wrote about experimental “vaccines” that the United States government has been working with pharmaceutical companies to develop — different ones for poultry and people. I asked if Department of Health and Human Services (HHS) Secretary Robert F. Kennedy, Jr. and Department of Agriculture (USDA) Secretary Brooke Rollins, both new to their jobs in February, would stand up against this and other aspects of “the US government’s bird flu scheme ramped up during the previous presidential administration.” Here is an update.
“The unfolding bird flu narrative serves as a chilling echo of the COVID-19 pandemic, starkly illustrating a playbook dusted off and redeployed,” wrote Joseph Mercola in the concluding paragraphs of his Friday article at mecola.com detailing the outrageous actions the United States government has been taking and is planning to take in the name of countering bird flu.
Even people who took one, two, or three experimental coronavirus “vaccine” shots during the height of the coronavirus scare are saying “nope” to taking any more “boosters.” Yet, behind the scenes, the United States government has kept funding companies in the pharmaceutical industry to continue developing new iterations of the unpopular “vaccines.”
Despite the health problems experimental coronavirus “vaccine” shots have caused many Americans, United States law has prevented victims from obtaining from the shots’ manufacturers compensation for the harm suffered.
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Polio Poppycock
“Polio.” That is a common go-to word for trying to silence people expressing any concern about any vaccine. The emotion-centered tactic relies on people having great fear of polio and great reverence for the polio vaccine commonly understood to have vanquished the disease. Voilà, all vaccines are wonderous medical tools, and anyone who questions them must want children to be struck by the horror of polio.
Though much pushed by government, companies, and media, the successive coronavirus “vaccine” shots have become increasingly unpopular. This includes among medical workers.
Most Americans are long past obsessing about fear of coronavirus. But, the United States government won’t give up on promoting the repeated injecting of experimental coronavirus “vaccine” shots, which have turned out to be neither safe nor effective, into every person in the country. And, yes, that even includes babies for whom the risk of death from coronavirus has been virtually nil.
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Moderna’s Bird Flu Shots Bonanza
On July 2, I wrote about the United States government’s new version of Operation Warp Speed undertaken in the name of countering bird flu. An early component of the new program for expedited bird flu mRNA shots development, I noted, involved the US government providing 176 million dollars to Moderna. All indications were that other companies would also be diving in for dollars as this program and other bird flu related government actions progress.