Scientists have long known that the gene-transfer technologies used in both the Pfizer and J & J COVID-19 vaccines were associated with systemic inflammation and the potential for viral DNA to get inserted into the DNA of body cells as well as reproductive cells. Insertion of the viral DNA coding for the spike protein into reproductive cells, such as eggs and sperm, would then be transmitted to your offspring.
While we were repeatedly told that there was no chance these vaccines could alter our DNA, a study from the winter of 2022 showed that the Pfizer vaccine caused human liver cells to copy the vaccine mRNA into DNA and insert it into the person’s DNA. This was not a surprise. Molecular biologists knew that this was likely. Further, they knew that insertion of viral DNA into the DNA of a person’s immune cells would increase their risks for leukemia. However, most stayed silent as large segments of our population were injected with this experimental gene-transfer technology.
“In 1999 18-year-old Jesse Gelsinger died when an experimental gene treatment designed to treat his metabolic liver disease sent his immune system into overdrive. A few years later, in 2003, researchers reported that several people treated for immunodeficiency developed leukemias, an unfortunate result of the virus randomly inserting its cargo into cancer-promoting regions of the genome.”
WAIT! WHAT??? Gene transfer technologies, such as those used with the COVID-19 vaccines are known to cause severe inflammatory responses and lead to cancer in some people??
YES. In fact, the Mayo Clinic lists the risks associated with gene therapy as follows:
- Unwanted immune system reaction. Your body’s immune system may see the newly introduced vaccine particles or the protein they produce as intruders and attack them. This may cause inflammation and, in severe cases, organ failure.
- Targeting the wrong cells. Because this technology can affect more than one type of cell, it’s possible that healthy cells may be damaged, causing other illness or diseases, such as cancer.
- Infection caused by the virus. It’s possible that once introduced into the body, the adenoviral vectors (such as J & J and Astra-Zeneca) may recover their original ability to cause disease.
- Possibility of causing a tumor. If the new genes get inserted in the wrong spot in your DNA, there is a chance that the insertion might lead to tumor formation.
In a recent meeting with AFLDS National State Leaders, Dr. Dana Granberg-Nill asked Dr. Christina Parks about the effects of the spike proteins in the COVID jabs. “When I think of the injuries caused by the spike proteins, I think it is inflammation-driven. Whether it’s the heart, whether it’s the nerves, whether it’s the skin, that that spike protein is causing an inflammation and sometimes and autoimmune response. Have you seen anything along the lines of soft tissue injuries or even bone fractures that are out of proportion to injury in kids?”
Dr. Parks agreed with Dr. Granberg-Nill that there is inflammation but points out there are many more mechanisms than inflammation at work. “When anything gets dysregulated, it causes inflammation,” Parks comments, “The adrenal and T-cell effects are somewhat driven by inflammation but they’re somewhat driven by some really core level dysregulations, not just inflammation. There’s evidence that it may bind major tumor suppressors. It allows huge DNA damage and possibly the formation of cancer cells.”
Parks recognized an earlier study on infants this highlights core dysregulation. “Remember we have that data in infants where when the mother had COVID or was vaccinated, when they were vaccinated it was way worse, but they had literally NO STEM CELLS, almost NONE. So, that’s not just inflammation. That’s a core dysregulation. It could be caused by some event where the cells blow up because of inflammation, but it is not just a standard form of inflammation. There is a lot more going on here.” Parks goes on to explain that our Toll-Like Receptors are down regulated. “That is not inflammation. That is immune suppression. That’s AIDS. So, you’ve got inflammation in conjunction with an autoimmune deficiency.
What’s happening is our T-cells are going anergic because of the chronic immune activation. Remember the spike protein keeps getting taken to our lymph nodes, where it keeps being presented, where it keeps causing activation of our T-cells.
Eventually, your body tells itself to stand down because you just can’t keep attacking yourself. The T-cells become anergic. If you keep stimulating them after they stand down and are anergic, you’ve got AIDS (autoimmune deficiency). Then, those T-cells actually signal the production of aberrant antibodies. They start signaling the production of auto-antibodies. There is a fair amount of research on that previously, with conditions like lupus.” Dr. Parks believes that is exactly what is happening here.
“Remember when your T-cells go anergic, you are NOT protecting the body against infection. Your T-cells are not working, and they are NOT surveilling for cancer.”
“So, you’ve got the disruption of p53’s (a major tumor-suppressor) at the same time your T-cells aren’t working to go around and kill the cancer cells AND the mRNA is going to get inserted into your stem cells. It’s going to get inserted into your DNA. It’s going to cause issues favorable for cancer. If your T-cells aren’t surveilling and killing those cancer cells, the likelihood of leukemias, lymphomas, and other cancers is just going to skyrocket. So, we’ve got really a perfect storm here.”
Largescale acceptance of gene-transfer technology is likely an important goal of both the FDA and pharmaceutical companies as there are currently more than 700 active investigational new drug applications for gene therapies currently waiting for FDA approval.
The number of gene therapy drugs waiting to be approved makes it more urgent that we understand what the oversight process currently is for these products.
All institutions that conduct experimental gene therapy must have oversight from an Institutional Biosafety Committee (IBC).
Did COVID-19 vaccines undergo this type of oversight, or were they exempted from testing due to being classified as a “vaccine?” This information needs to be made public immediately.
Gene therapy technologies are supposed to be extensively tested for
- Whether they cause a hyper-inflammatory response
- Whether they stimulate the immune system to attack cells making the new protein
- Their effects on fertility
- Whether the viral DNA inserts into the person’s DNA
- Whether viral DNA inserts into the DNA of the person’s eggs or sperm
- Whether the treatment results in the promotion of cancer
How the body handles and excretes the nano-lipid particles/adenoviral vector as well as the protein that is produced is also supposed to be extensively tested.
Where these experiments done? What was found?
If the COVID-19 vaccines were not subject to the normal regulatory oversight process, why not?
Would our government, in conjunction with Pfizer, Moderna and J & J, really use semantics (calling them “vaccines” rather than gene therapy technology) as a way to bypass critical safety reviews??
Pfizer, Moderna, J & J, the NIH and the FDA need to answer these questions.
The American public and all of humanity need to know the answers!
https://osp.od.nih.gov/implementation-of-the-nih-policy-for-data-management-and-sharing/
