A double blind placebo trial is how safety gets established for a pharmaceutical product. You take ten thousand people, five thousand get the drug, five thousand get a placebo, which by definition should have no effect on the body. For an injectable product, that placebo should be saline. It's called double blind because neither the scientists running the study or the patients receiving it know who got which one, and that distinction matters because those scientists are being paid by the drug company the entire time.
That is the standard for every drug, every cancer treatment, every product we put in our bodies. Except one.
One of the things I've proven through years of lawsuits with our nonprofit is that not a single childhood vaccine on the schedule has ever gone through that process. None of them. That is the core of my entire issue with this. Of everything you could rush to market without proving it safe first, why would it be the product given to a perfectly healthy child?
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1September 6, 2026 1.4K 31
