re: What most of you already know about the vaccine.

define developed? Haven't they for years been trying to get that sort of technology "FDA" approved? Had Moderna up to this point had anything in it's history approved? Could you update us on how the trials are going for this?

Anyone have the numbers on Big Pharma's money made vs paid out in lawsuits? Guess which side always wins?

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Do I have any legal retribution if I am hurt by the ‘vaccine’?

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You will not get an answer to this. And that, gives you your answer.

You can also ask him whar are the long-term side effects of these gene therapy drugs. They will not answer because they CANNOT answer or they'll lie through their f*cking teeth because they don’t have the first f*cking clue

Antibody Dependent Enhancement (ADE) from Sharyl Attkisson. Vaxers will hate it, Anti Vaxers will call it a gotcha. It is information from a study about why vaxed people could be getting sick. LINK

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Do you think that this shot, which uses your own cellular machinery to create a viral spike protein, is more unsafe than a virus that uses the same cellular machinery to make the same viral spike protein?

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I survived the virus and don't have to take both risks.

My survival of the virus is a known quantity.
My reaction to the jab is not.
Why risk it?

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if there is even one M.D. out there that says this shot is unsafe, does this destroy your "M.D. Narrative?"

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It's not a narrative. It was a specific response to the statement responded to. Context is important.

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Neither can you

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Actually, I kinda can. While this isn’t certain, here is the theory:


A coronavirus (CoV) infects the target cell by either cytoplasmic or endosomal membrane fusion. No matter what path it chooses, the final step of viral entry involves the release of RNA into the cytoplasm for replication. Therefore, the fusion capacity of the CoV-S is a leading indicator of infectivity of the corresponding virus. In order to bind a host cell, CoV-S needs to be primed through cleavage at sites on the spike protein via a ‘ molecular scissors ’ called furin that essentially trims a spike protein to get it ready to bind.
More furin cuts mean more spike proteins primed to enter human cells. In SARS-CoV, (original SARS) less than 10% of spike proteins are primed. In SARS-CoV-2, that percentage rises to 50%. In the Alpha variant, it’s more than 50%. In the Delta variant, greater than 75% of spikes are primed to infect a human cell. So, more viruses enter and replicate. That’s why in delta the viral loads are much higher. The increase in efficiency of furin cuts is thought to be via the P681R mutation, as that is a hallmark of the Delta strain. It vastly increases efficiency of furin cuts.

I didn’t learn this on youtube. So, no sweet video. Sorry.

But hey, bIG pHaRmA ???? $$, right??

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I survived the virus and don’t have to take both risks

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Fair statement.

Not the same as saying the vaccine sucks or that no one should take it or that it doesn’t work or whatever else.

And, the statement also needs to be qualified. It is not yet clear that the immunity from having it is durable. Please note that I did not say that the immunity form the shot is.
Coronaviruses have typically not conferred long term immunity. Maybe this one will, but antibody levels decline for sure. The antibody levels of recovered sick fell in the range above 1 shot mRNA recipients and below 2 shot recipients. The real winners were recovered sick plus 1 shot. They had vastly higher titers than anyone. For me, if I’d had it and based on current info, I’d wait 9-12 months and get one shot and stop

For someone who has not had it, the question remains.:
Do I want my cellular machinery to make one protein from the virus, or do I want my cellular machinery to make ALL the proteins of the virus - including the one above- in vastly larger numbers. Which seems safer? Again, that’s the only question.

BTW, I’m not saying there isn’t an argument. But, to me, it has to address this specific question.