A toxicologist’s devastating testimony on how COVID-19 mRNA vaccines could cause cancer and alter the human gene pool. This is a must-read. Dr. Lindsay Janci just laid out a harrowing case. The concern isn’t just short-term side effects; it’s the potential for genetic vaccines to drive cancer and be passed to future generations. Her summary is a masterclass in scientific alarm.

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Here are the 9+ potential pathways to cancer she detailed:

1. LNP Delivery to Stem Cells: Lipid Nanoparticles (LNPs) don’t just go to muscle cells. They readily transfect hemopoietic stem cells—the origin of all our blood cells.
2. Cancer Metastasis: LNPs may cause pre-existing cancer cells to spread more easily by inducing “endothelial leakiness.”
3. Inherent LNP Oncogenicity: The LNPs themselves might have cancer-causing effects, which have never been studied.
4. The SV40 Promoter: Hidden plasmid DNA in the vaccines contains the powerful SV40 promoter. If this genetic switch integrates near an oncogene, it could explosively drive cancer growth.
5. SV40 Enhancer (Nuclear Targeting): This sequence is designed to rush DNA into the cell nucleus—a key step for “insertional mutagenesis,” where foreign DNA disrupts our own genes.
6. Spike Protein & p53: The spike protein itself has been shown to inhibit p53, a critical tumor suppressor protein that stops cancer from developing.
7. Insertional Mutagenesis & Frameshifts: Plasmid DNA doesn’t need SV40 to get into the nucleus. Once integrated, it can cause frameshift mutations, leading to aberrant, cancer-causing proteins.
8. mRNA Reverse Transcription: The mRNA can be reverse-transcribed back into DNA and integrated into our genome, a known cancer mechanism, especially in ovaries & testes where reverse transcriptase is high.
9. Immunosuppression: The vaccines may suppress specialized T-cells that act as “guards” keeping dormant cancer clones in check. Weakening this guard can lead to a surge in cancers, similar to what we see in aging pets.

But it gets worse. Dr. Janci issued a grave warning about heritable genetic damage:

The DNA plasmids and reverse-transcribed DNA can potentially integrate into sperm and ova (gametes). This means the genetic payload could be passed to our children and “contaminate the gene pool.”

She reveals two mechanisms:

• Genomic Integration: Direct insertion into the gamete’s DNA, likely causing cancer in offspring rather than functional spike production.

. Sperm-Mediated Gene Transfer (SMGT): A process where sperm can carry extra-chromosomal DNA and pass it on to the next generation without full genomic integration, leading to constitutive spike protein expression in children.