Excerpt from an interview with a genetics expert Professor Dolores Cahill. The full 5:45 min interview may be found on YouTube while it still survives. This excerpt is available on Rumble.
I suppose there are three waves of adverse events (from messenger RNA or mRNA vaccines developed by Moderna, Pfizer).
There are adverse events like anaphylaxis (severe, potentially life-threatening allergic reaction) in the first week. Therefore, these vaccines shouldn’t be given in the 2nd dose. They have planned a lot of them as two doses.
Then the real adverse events will happen, whatever the mRNA is in the vaccines, when the (vaccinated) person comes across that (ie. a coronavirus). It could be in February or March 2021 or a year later …. that would be when in the animal studies, 20% or 50% or 100% of the animals died!
I am also saying that people over 80 who get these, maybe about 2.5% will experience severe side effects. One in 40 people will experience adverse events where they cannot work or live life normally.
Then with the 2nd vaccination it could be 1 in 10 or ten percent. For the over 80-year-olds or 75-year-olds, I would think that 80% of them would have life-limiting adverse events or die when they come across the mRNA again.
For others (not elderly) it could be half of the people who could be severely harmed.
What it does is… this gene therapy or medical device is setting up an autoimmune disease … chronically. It’s like injecting people who have nut allergies with peanuts.
It’s anaphylaxis in the first wave. It’s anaphylaxis +allergic reaction the 2nd wave. But the 3rd reaction occurs when you come across whatever the messenger RNA is against (virus, bacterium, etc.). And now you have stimulated your immune system to have a low-grade autoimmune disease, not immunity to yourself per se because the mRNA is expressing a viral protein.
You are making yourself a genetically modified organism, and so the immune system that is meant to push the viruses or bacteria out… now the autoimmune reaction is attacking your body low grade.
Now (months later) when you come across the virus later in February or March that stimulates the immune system to get rid of the virus and then it (the immune system) suddenly sees that you have viral proteins in your own cells and organs, then about a week later (the adaptive immune system kicks in, the mechanism that makes specific long-term memory antibodies against a pathogen) and you go into organ failure. Because your immune system is killing your own organs. Those patients will present as sepsis initially. Then (later) you die of organ failure.
If you have one or two co-morbidities, the energy the immune system requires to boost your immune system will make them (older persons) very tired and exhausted and they don’t have the capacity to survive if they have underlying conditions.
Normally, because the mRNA is in every cell of their body, it’s almost unstoppable. It destroys the heart, or the spleen, or the lungs, or the liver because the mRNA is expressing the protein in every cell.
Just as a solution, what we urgently need, is a repository, 1 in 100, or 1 in 200 vaccine vials injected, to be set aside, especially into the elderly in the care homes. They need to be stored in a biorepository of the vaccine vials randomly, so when the people begin to die, we can actually see what is in this vaccine. We should be doing this now.
I am concerned that there are maybe multiple mRNAs in this vaccine, not just something for coronavirus. If it is influenza or other viruses, we would be priming these people to other natural (cold and flu) viruses that are circulating.
We urgently need quality control to randomly require doctors to give 1 in 100 vaccine vials to a repository and someone like me could forensically analyze what’s in these vaccines. So, when the elderly start dying, we will know. We should be knowing now what’s in them.
It’s absolutely a dangerous gene therapy. Should not be given to the elderly.
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