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Tom Childs's avatar

Thank you Geert,

Your work is turning heads.

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Possum's avatar

The lipid nanoparticle, cytotoxic synthetic spike protein enters the nucleus of the cells, down regulating DNA repair, degrading and subverting the immune system. The vaccine spike is the Wuhan strain.

The virus spike protein (omicron has 30 odd alterations/mutations in the head of the spike protein), has the furin cleavage site (gain of function giveaway), in both virus the vaccine spike protein, both are synthetic and cytotoxic. I sense that the vaccine spike, though nearly identical is worse.

The vaccine spike protein once in the cells, converts into DNA. The cells then produce more spike protein which is foreign to the innate/adaptive immune system. This causes inflammation.

The immune system is now tired and battle weary, leaving it vulnerable to whatever. Vaccine Induced Immune Deficiency Syndrome will occur with boosters.

The non sterilising, out of date, most poorly deployed, experimental mRNA gene therapy “vaccine” and boosters are causing vaccine resistance, negative efficacy, viral immune escape variants, disease enhancement and ADEI, antibody dependent enhancement infection. This outcome is disaster for the immune system. Consequently this is causing dormant retroviruses like shingles and herpes to re-emerge. Tuberculosis and hepatitis are also dormant retroviruses. Vaccine induced autoimmune CD8 T-cell dependent hepatitis is recently new and could be due or partly due to vaccine shedding.

Life insurance claims have recently shot up 40%. Cancer, autoimmune, prions, heart, stroke, etc. Monkey pox vaccine available now in Australia. Monkey pox cooked in a lab, Dr John Campbell YouTube. Also very similar to vaccine induced retroviruses, shingles etc. Look ambiguous?

I wouldn’t be in a hurry to partake in this medical experiment or the next medical experiment.

How can you have a gain of function vaccine for a gain of function virus!?

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