Can DNA vaccine contamination explain the rise in cancer rates and autoimmune diseases?
A conversation with pathologist Dr. Ryan Cole
In a recent
episode of “American Thought Leaders,” host Jan Jekielek speaks with Dr. Ryan Cole, a pathologist and an expert on SARS-CoV-2 and the mechanisms of the genetic injections labeled as vaccines. Here, they discuss how these COVID-19 genetic vaccines may be related to the rise in cancers and autoimmune diseases.
Jan Jekielek: I’ve done an interview with Kevin McKernan about what’s in the vaccine vials, this contamination that multiple labs had already verified. Let’s start with that, because that’s something you’ve been covering.
Dr. Ryan Cole: Many laboratories around the world have been looking at this issue, and Kevin has been a leader in this area. When these products were made, there was the J&J, that’s an adenovirus factor, but then there was Moderna and Pfizer. These are mRNA; synthetically engineered, modified RNA.
For the trials, at least for Pfizer, there’s a synthetic PCR-type process in making up the mRNA sequence for these shots. That was given to 40,000 people, and was a deliberate, synthetic, engineered attempt at a precision-type process.
Mr. Jekielek: That’s dubbed “Process 1”?
Dr. Cole: Yes. To make a lot of this for billions of people, a second process was used, which was only tested on about 252 people instead of 40,000. That was taking this complementary DNA sequence that is the reverse pattern of the spike to make mRNA a message, and then your body would make that protein in your cells.
We did the trials on this very controlled synthetic process, but then at the last minute they snuck under the radar and said, “But we’re going to make all the rest of them using a process we’ve barely tested.” That’s what got rolled out into billions of people’s arms. It was kind of a bait and switch. Those large data sets one would want to see in terms of harms, you’re not going to find that in 250 patients.
Mr. Jekielek: They actually use E. Coli, a bacterium, to grow these plasmids of DNA, which can then be turned into the RNA, but they just didn’t clean them up.
Dr. Cole: They didn’t clean them up properly. They’re supposed to put in an enzyme that breaks down any residual DNA. Even up to the current vials of the fall booster, the XBB 1.5, Kevin and 12 other laboratories have shown there is still bacterial plasmid DNA contamination within these vials. The FDA allows up to, in gene products, 10 nanograms of DNA per dose, but that’s based on old technology.
The smaller the fragment of DNA, the greater the opportunity it has to intercalate into your own DNA as well. More testing and probes are still needed to prove this, but it explains a lot of the strange happenings we’re seeing in clots, autoimmune disease, and cancers, because we’re changing signals within cells. Human cells are meant to make human proteins. They’re not meant to make foreign proteins. When we program people’s cells to make things they’re not supposed to make, they can go haywire. They can mutate and become a target of our own immune system.
My big concern is that billions of people around the world have received a product that was contaminated, which was admitted to by the Canadian health regulatory agency.
Mr. Jekielek: It was Epoch Times reporting that caused that disclosure to happen.
Dr. Cole: Yes, well done. And my concern isn’t just these COVID shots. It’s this entire technology. A lipid nanoparticle in and of itself is an unproven product. It takes on whatever you put into it. They’re trying to create them for RSV, flu, and for many other pathogens. It still takes those little gene sequences anywhere and everywhere in the body.
In some of his autopsy findings, the late Dr. Burkhardt, a friend and mentor to me, showed spike protein in the testes, in the placenta, and in the uterus. I’ve seen some of those in the studies we were doing in my laboratory.
Mr. Jekielek: You feel this provides some explanation for these turbo cancers and this clotting we’ve been seeing.
Dr. Cole: Dr. Ute Krüger from Sweden coined the term turbo cancer. She’s a breast pathologist who was looking at the damage of these shots. She noticed increases in cancer, an uptick not only in the size of the cancers, but also in the stage of the cancers. Instead of just taking out a lesion, she was finding it had spread to lymph nodes, the liver, the bone marrow, and the brain. She was seeing cancers behave in a manner like never before. Everywhere I go, I hear oncologists and physicians telling this story.
A prominent oncologist in Texas told me, “At first I saw the clots, then the blood cancers, the leukemias, and the lymphomas. Now, I’m seeing solid tissue cancers at rates I’ve never seen. Patients that were stable or cancer-free for 1, 2, 5, or 10 years, their cancer is now back, and it’s not responding to traditional therapies.”
It’s not necessarily that the gene sequence is causing cancer. The gene sequence can cause some of the mutations that lead to cancer. But it’s also suppressing the immune system, and your immune system is what kills cancer. If your immune system is asleep, your killer cells can’t be activated
In addition, there are so many basic things our public health system isn’t addressing. Do we have a horrible diet? Are we vitamin D-deficient? Absolutely. In addition, a lot of people received a contaminated adulterated gene-based product, and we don’t know the long-term outcomes.
Mr. Jekielek: Ryan, any final thoughts as we finish up?
Dr. Cole: If we can resolve conflicts by having face-to-face conversations, the world will be a better place, and maintaining our rights to speak and think freely is more important than anything. Stay positive. Stay optimistic. Life is still good.
This interview has been edited for clarity and brevity.
