Dr. Karina Whitehouse Presentation on mRNA \/_xines

Karina Acevedo-Whitehouse 5 minute discussion of mRNA \/@<<ines.

This was a live presentation to the General Assembly Meeting #76 on February 13, 2023 by professor Karina Acevedo-Whitehouse in which she presented her shocking new paper (Jan, 2023) on the adverse effects of synthetic mRNA.(1)

Header image: Courtesy of Karina Acevedo Whitehouse and Claudio Fabián Guevara at DiariodeVallarta.com.

Are You Questioning the Safety of mRNA \/a<<ines?
Just watch this:

The 8 Points of the Above Presentation by Professor Karina Acevedo Whitehouse World Council for Health:

1) mRNA immunization is a form of gene therapy as it involves exogenous mRNA based gene expression.

2) \/a<<ine mRNA-NLP (nano-lipid-particles) are distributed throughout the body after Intra-Muscular injection of the \/@<<ine.  It does not stay at the injection site, and/or stay in remaining lymph nodes. Hours after injection these NLP particles are distributed to various organs, and cross the BBB (blood brain barrier) and enter the brain.  Autopsy studies done in mice after mRNA injection shows brown immuno-staining Spike protein in various organs and brain.

3) \/a<<ine mRNA persists within the cells for at least 6 months, and remains viable, producing spike protein continuously with no off switch. There is no control of the exact spike protein dosage. The spike protein is highly toxic and can explain many of the human reactions to these products.

4) \/a<<ine mRNA drives intracellular cascades which can cause autoimmunity, autoinflammation, DNA damage, genomic and chromosomal instability
and cellular degeneration. This also causes ribosomal frame shift mutations, and insertional mutagenesis. These intracellular cascades were not studied prior to EUA (emergency use authorization).

5) An unprecedented rate of adverse effects has been reported in European data updated to July 21, showing one million three hundred thousand (1,300,000) adverse reactions after the Phizer  \/a<<ine, and nearly 400,000 with M0derna. This is absolutely unprecedented.  Compared to influenza \/a<<ine, the adverse event rate for the mRNA \/a<<ines are 135 times greater (per month) then the adverse event rate of the influenza \/a<<ine.

6) Self amplifying mRNA immunization is a very bad idea. It has never been used for \/a<<ines.  This involves adding a “replicase gene” to the delivery gene, allowing for amplification of the mRNA production of the delivery gene (spike protein). Again, there is no way to control the exact dosage of this mRNA production of a foreign protein product which may continue indefinitely. This has never been studied for long term safety.

7) Development and delivery of mRNA \/a<<ines in 100 days. This is much too short a time to evaluate for safety, and is prone to serious manufacturing problems (i.e., DNA contamination which causes insertional mutagenesis (a direct cause of cancer). Excess mortality after mRNA \/a<<ination has been reported in various countries.  Post mRNA \/a<<ination data from the United States shows increased sudden cardiac death, cerebrovascular diseases,  and excess death due to cancer.

8) Procuring and maintaining health can be done without gene therapy mRNA \/a<<ines. There are various ways we can boost our immune system. Why not invest in health instead of experimenting on our fellow humans? For example, early treatment with repurposed anti-viral drugs such as Ivermectin, Zinc, Hydroxychloroquine, Cannabidiol, etc. is highly effective and has shown success in preventing hospitalizations and death from viral disease in many other countries adopting early treatment.

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=======================================================Karina Acevedo-Whitehouse: The Impact of Synthetic mRNA on Health

Speaking live at General Assembly Meeting #76 on February 13, professor Karina Acevedo-Whitehouse presented her shocking new paper on the true impact synthetic mRNA has on health, and answered questions from the audience.

Download Karina’s slides.

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References

1) Acevedo-Whitehouse, K., and R. Bruno. “Potential health risks of mRNA-based vaccine therapy: a hypothesis.” Medical Hypotheses 171 (2023): 111015.

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