Schwere neurologische Krankheiten wie Alzheimer verursacht von mRNA Impfstoffen

„In einem schockierenden neuen Bericht über die COVID-19-Impfstoffe wurde festgestellt, dass der Pfizer-Coronavirus-Impfstoff langfristige gesundheitliche Auswirkungen haben kann, die zuvor nicht bekannt waren, einschließlich „ALS, Alzheimer und anderen neurologischen degenerativen Erkrankungen“. (…)

Die Zusammenfassung des Berichts kommt zu dem Schluss, dass

„Der erhobene Befund sowie zusätzliche potenzielle Risiken lassen den Autor glauben, dass die behördliche Zulassung der RNA-basierten Impfstoffe gegen SARS-CoV-2 verfrüht war und der Impfstoff viel mehr Schaden als Nutzen anrichten kann.“

Der Bericht selbst endet mit dieser Warnung:

„Der Impfstoff könnte eine Biowaffe sein und noch gefährlicher als die ursprüngliche Infektion.“

(Approving a vaccine, utilizing novel RNA technology without extensive testing is extremely dangerous. The vaccine could be a bioweapon and even more dangerous than the original infection.)„

Hier das Abstract des erwähnten wissenschaftlichen Artikels:

„ABSTRACT

Development of new vaccine technology has been plagued with problems in the past. The current RNA based SARSCoV-2 vaccines were approved in the US using an emergency order without extensive long term safety testing. In this paper the Pfizer COVID-19 vaccine was evaluated for the potential to induce prion-based disease in vaccine recipients. The RNA sequence of the vaccine as well as the spike protein target interaction were analyzed for the potential to convert intracellular RNA binding proteins TAR DNA binding protein (TDP-43) and Fused in Sarcoma (FUS) into their pathologic prion conformations. The results indicate that the vaccine RNA has specific sequences that may induce TDP-43 and FUS to fold into their pathologic prion confirmations. In the current analysis a total of sixteen UG tandem repeats (ΨGΨG) were identified and additional UG (ΨG) rich sequences were identified. Two GGΨA sequences were found. Potential G Quadruplex sequences are possibly present but a more sophisticated computer program is needed to verify these. Furthermore, the spike protein, created by the translation of the vaccine RNA, binds angiotensin converting enzyme 2 (ACE2), a zinc containing enzyme. This interaction has the potential to increase intracellular zinc. Zinc ions have been shown to cause the transformation of TDP-43 to its pathologic prion configuration. The folding of TDP-43 and FUS into their pathologic prion confirmations is known to cause ALS, front temporal lobar degeneration, Alzheimer’s disease and other neurological degenerative diseases. The enclosed finding as well as additional potential risks leads the author to believe that regulatory approval of the RNA based vaccines for SARS-CoV-2 was premature and that the vaccine may cause much more harm than benefit.“

Quelle: Blauer Bote Magazin und im Text angegebene Links