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There's no way that the FDA/CDC is properly staffed to do thorough analyses of all the VAERS, vSafe and VSD records streaming in. We should simply assume they are overwhelmed and publicly offer help. Of course they will decline but it would draw attention to the high volume of adverse events being reported.

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You mean Steve and his team can do it but FDA/CDC can't? Maybe they don't want to... but I highly doubt that they are not capable.

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