Malone & Bourla & Bancel Sahin Weissman et al. in their work with mRNA technology for vaccines etc. & the exosome extracellular vehicle lipid-nano particle (LNP) molecular transport system KNEW,

these animals knew, these demonic beasts knew that they needed the LNP exosome delivery type system to get the mRNA from the deltoid etc. & knew it was deadly to the reproductive system, baby in utero

These feral devil animals KNEW! They did not care! About the developing child. Just NOBELS. And fame and money, your money! They always knew the mRNA-LNP platform was unsafe and especially to the reproductive tract…why was Malone silent on this? Or Bourla? Or Bancel? Or Weissman? They KNEW! The date on this paper was 2018.

This is why no mRNA vaccine, not now, and not ‘new and improved’ can EVER be safe for the very mechanism of the molecular transporter fatty ball, the lipid transport ball or LNP as we know it, what houses the mRNA payload, is very toxic on its own…

this is separate from the mRNA itself and its dangerous actions e.g. inducing/translation to spike protein that is an endothelial pathogen, that is cancer causing, with boosting that causes IgG4 class switch that inhibits routine tumor suppressor binding and thus cancer escalation etc.

did these beelzebubs from Pfizer and Eli Lilly tell POTUS Trump this and RFK Jr. this at their dinner in Mar-a-Lago? Or did that escape them?

Potential adverse effects of nanoparticles on the reproductive system - PMC

Key statement by researchers:

‘Previous studies have shown that numerous types of NPs are able to pass certain biological barriers and exert toxic effects on crucial organs, such as the brain, liver, and kidney.

Only recently, attention has been directed toward the reproductive toxicity of nanomaterials. NPs can pass through the blood–testis barrier, placental barrier, and epithelial barrier, which protect reproductive tissues, and then accumulate in reproductive organs.

NP accumulation damages organs (testis, epididymis, ovary, and uterus) by destroying Sertoli cells, Leydig cells, and germ cells, causing reproductive organ dysfunction that adversely affects sperm quality, quantity, morphology, and motility or reduces the number of mature oocytes and disrupts primary and secondary follicular development. In addition, NPs can disrupt the levels of secreted hormones, causing changes in sexual behavior.’

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