Hi Hedley, I’ve been under the impression that these shots have been contaminated with DNA. There is another school of thought that there isn’t any MRNA in the shots but there are DNA Plasmids that instruct bacteria (e.Coli) and yeast to manufacture the Spike Protien in our bodies thus effecting people in different ways according to varying levels of bacteria and yeast. The components for these shots have been around for a long time, ie No Warp speed. What are your thoughts? Cheers Phil
Thanks Phil, great question! Yes, Yes, Yes "DNA Plasmids that instruct bacteria (e.Coli) and yeast to manufacture the Spike Protien in our bodies thus effecting people in different ways according to varying levels of bacteria and yeast." Spot on! Both mRNA injections, and viral vectors (AstraZeneca adenovirus) are gene modified cell therapy. They use CRISPR technology, which is effectively genetic engineering. First on the market was Novartis' Kymriah in 2017 - here are the side effects: https://www.fda.gov/media/107296/download It's been a con all along, just a rebranding of existing drugs for blood cancers as vaccines!
Rand Paul has been on track from the beginning. Those responsible for the vaccines should never have been able to police themselves, $$ was used to inject the fear into the media, and medical professions. Greed spun the web of deception into our lives, making a mockery of the health care system, doctors are no longer trusted to vaccinate children, or adults, let alone treat people. I myself trust none. I’ll die of something, but that’s in God’s hands.
..."You can't shortcut on quality in the supply chain"...then why did it happen? Does Pig Pharma not know from previous experience that you cannot cut corners? Of course they know and still blatantly allowed corners to be severely cut. Even the trials were a complete farce.
Another deception post pushing people away from premeditated plandemic towards incompetence/accidentic. The difference in a sentence of accidental homicide and murder is death. Don't fall for it.
Thanks for the additional insight. The FDA EUAs list a set of criteria that Pfizer and Moderna have to follow including following cGMP. It’s apparent as you’ve stated that they have not met the criteria. Isn’t the FDA obligated by law to withdraw these products under these circumstances? By the way, is your pharmaflow email still current in the event you are contacted.
Hear, hear! Hedley maybe thinks the corner cutting is the main problem, rather than the concept of trojan horses infiltrating and hijacking cells to produce even more foreign toxins.
It's both Markker - see the answer to Phil's comment. The supply chain for CAR T therapies such as Kymriah is impossible to keep safe - the production process is far too complex and variable. I consulted on the Kymria drug substance in 2013, but I never thought 4 years later FDA would approve it as a viable drug - it was fraudulent, therefore actionable in law, only no lawyers want to accept the case - I've even told Arron Siri what I know, no charge, and he ignores me :O(
As you have reported on before, these injections were failed cancer treatments which got rebranded into lifesaving vaccines in order to save the pharma industry and the world needed to be made frightened to death, almost, of a new disease which only a "vaccine" would save the world (and cause more illness, necessitating more pharma product sales). The only way these ineffectual and dangerous products got released was by EUA. Does not explain how all regulators already knew dangers, are ignoring all safety signals, and still promoting for most vunerable in society, does it? Or, for Siri and others, to be ignoring lots of people like yourself. Just read about spraying the sky with this stuff and the planes are back spraying Yorkshire again!
Think they are desperate now Markker! Yes, that's exactly what happened, re-branded failed drugs for rare cancers costing c. $400,000 per patient, with horrible side effects. Patents have expired on all the big pharma's drugs except for the CAR T therapies. They knew this 10+ years ago, and with the help of Billy boy Gates, they got it done...
Endotoxin contamination is a major concern in Genetic Modification of B-cell Acute Lymphoblastic Leukemia patients own T cells and injection of the product
Hi Hedley, I’ve been under the impression that these shots have been contaminated with DNA. There is another school of thought that there isn’t any MRNA in the shots but there are DNA Plasmids that instruct bacteria (e.Coli) and yeast to manufacture the Spike Protien in our bodies thus effecting people in different ways according to varying levels of bacteria and yeast. The components for these shots have been around for a long time, ie No Warp speed. What are your thoughts? Cheers Phil
Thanks Phil, great question! Yes, Yes, Yes "DNA Plasmids that instruct bacteria (e.Coli) and yeast to manufacture the Spike Protien in our bodies thus effecting people in different ways according to varying levels of bacteria and yeast." Spot on! Both mRNA injections, and viral vectors (AstraZeneca adenovirus) are gene modified cell therapy. They use CRISPR technology, which is effectively genetic engineering. First on the market was Novartis' Kymriah in 2017 - here are the side effects: https://www.fda.gov/media/107296/download It's been a con all along, just a rebranding of existing drugs for blood cancers as vaccines!
How can trust ever be restored. Its not in me to trust anymore.
Rand Paul has been on track from the beginning. Those responsible for the vaccines should never have been able to police themselves, $$ was used to inject the fear into the media, and medical professions. Greed spun the web of deception into our lives, making a mockery of the health care system, doctors are no longer trusted to vaccinate children, or adults, let alone treat people. I myself trust none. I’ll die of something, but that’s in God’s hands.
Nice post Jeanette! Agree...
Very well worded sentiments which people should take notice of.
..."You can't shortcut on quality in the supply chain"...then why did it happen? Does Pig Pharma not know from previous experience that you cannot cut corners? Of course they know and still blatantly allowed corners to be severely cut. Even the trials were a complete farce.
Spot on, but the FDA et al have been infiltrated by Gates, so regulation is out the window…
Another deception post pushing people away from premeditated plandemic towards incompetence/accidentic. The difference in a sentence of accidental homicide and murder is death. Don't fall for it.
Incompetence with a purpose.
The alternative is to get healthy as we know that unhealthy people get sick.
Thanks for the additional insight. The FDA EUAs list a set of criteria that Pfizer and Moderna have to follow including following cGMP. It’s apparent as you’ve stated that they have not met the criteria. Isn’t the FDA obligated by law to withdraw these products under these circumstances? By the way, is your pharmaflow email still current in the event you are contacted.
Pharmaflow is still alive and kicking!
Absolutely, but Peter Marks was parachuted in to wave the jabs through https://www.fda.gov/about-fda/fda-organization/peter-marks even his staff don’t agree with him!
Thanks Hedley. Your post has provoked some fascinating responses to which you have replied with further elucidation.
They're all toxic.
Hear, hear! Hedley maybe thinks the corner cutting is the main problem, rather than the concept of trojan horses infiltrating and hijacking cells to produce even more foreign toxins.
It's both Markker - see the answer to Phil's comment. The supply chain for CAR T therapies such as Kymriah is impossible to keep safe - the production process is far too complex and variable. I consulted on the Kymria drug substance in 2013, but I never thought 4 years later FDA would approve it as a viable drug - it was fraudulent, therefore actionable in law, only no lawyers want to accept the case - I've even told Arron Siri what I know, no charge, and he ignores me :O(
As you have reported on before, these injections were failed cancer treatments which got rebranded into lifesaving vaccines in order to save the pharma industry and the world needed to be made frightened to death, almost, of a new disease which only a "vaccine" would save the world (and cause more illness, necessitating more pharma product sales). The only way these ineffectual and dangerous products got released was by EUA. Does not explain how all regulators already knew dangers, are ignoring all safety signals, and still promoting for most vunerable in society, does it? Or, for Siri and others, to be ignoring lots of people like yourself. Just read about spraying the sky with this stuff and the planes are back spraying Yorkshire again!
Think they are desperate now Markker! Yes, that's exactly what happened, re-branded failed drugs for rare cancers costing c. $400,000 per patient, with horrible side effects. Patents have expired on all the big pharma's drugs except for the CAR T therapies. They knew this 10+ years ago, and with the help of Billy boy Gates, they got it done...
More on Kymriah Deaths and Injuries
Endotoxin contamination is a major concern in Genetic Modification of B-cell Acute Lymphoblastic Leukemia patients own T cells and injection of the product
https://geoffpain.substack.com/p/kymriah-tisagenlecleucel-gmo-t-cell