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Broken civilizations get rebuilt at the local community level as families, businesses, churches and small civil governments begin to learn what those local institutions can be. That is happening right now in the US, primarily in rural counties.

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Dr. Peter McCullough Defines Bird Flu Mischief

1. Practice of culling (mass destruction of entire healthy flocks) when a PCR test is found positive to “eradicate” the virus is futile and may work to constrain the food supply. The current strain H5N1 clade 2.3.4.4.b is not thus far causing necropsy or radiographic confirmed fatal pneumonia in birds or mammals.

2. H5N1 host range expansion into migratory birds and mammals likely occurred as a result of gain-of-function serial passage research and a lab leak.

3. Increased transmissibility of H5N1 has a tradeoff of decreased virulence. Using legacy human mortality rates from cases in Southeast Asia is not appropriate. The US has never had a fatal human case of bird flu.

4. Fear-mongering promulgated by the Bio-Pharmaceutical Complex is designed to promote mass vaccination of animals and humans with lucrative pre-purchased contracts to the vaccine manufacturers and their NGO backers. Mass vaccination into a highly prevalent pandemic since it promotes resistant strains of the virus in the vaccinated.

5. If human-to-human spread occurs in the future as expected by many, it will be the product of gain-of-function research that has gone on for years with the goal of creating harm to human populations.

6. Be prepared with early prevention and treatment strategies on hand.

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No 'black box' warning for Covid mRNA vaccines?

The FDA has rejected its strongest safety warning for Covid mRNA vaccines despite acknowledging that children were killed by the products.

This news surfaced during a televised Bloomberg interview with FDA Commissioner Marty Makary, who said the agency has “no plans” to apply its strongest safety warning to Covid mRNA vaccines.

In that interview, Makary confirmed that the FDA’s own safety and epidemiology centre had formally recommended a boxed warning — a step reserved, under FDA rules, for drugs with “special problems, particularly ones that may lead to death or serious injury.”

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