Watch on Streamyard here > Speaking with Dr Shankara Chetty (South Africa) after his debut on GB News (UK) with over 400,000 views on Twitter! Is it time for an open, frank discussion about COVID-19? Quote from Dr Chetty: 'No hospitalisations, no deaths, no need for oxygen in my practice, and I've clearly negated that need for a vaccination to solve the problem.'
The beginning of the implementation of "their" plan to KILL HCQ AND STEROIDS etc, to kill early covid treatment and effective emergency room (as Dr Chetty's protocols) and hospital covid treatment, to push remdesivir and the vaccine only path is documented here https://apps.who.int/iris/bitstream/handle/10665/330680/WHO-HEO-RDBlueprint%28nCoV%29-2020.1-eng.pdf?sequence=1 WHO R&D Blueprint Informal consultation on prioritization of candidate therapeutic agents for use in novel coronavirus 2019 infection Geneva, Switzerland, 24 January 2020 - Coronavirus Outline of designs for experimental vaccines and therapeutics Draft version Jan 27, 2020
They "KILLED" steroids while the document acknowledges "although there is evidence of efficacy in the setting of severe illness".
The US representative at this Jan 2020 meeting was fauci stand in Hilary Marston - Medical Officer and Policy Advisor National Institute of Allergy and Infectious Diseases" with a big pharma "fixer" "McKinsey & Company and .. Bill & Melinda Gates Foundation" employment background.
I've been a huge fan of both of you and Dr. Shankara Chetty. I remember when he was treating his patient's, who had to walk for miles and miles, outside his clinic in a tent. All the while mercenaries were robbing and burning down all the HCQ. Sending my sincerest appreciation. Thank you both very, very much. PS I was researching medicinal Artemisia in the O Chem lab at the time. I grow a species of it : ) and give it away. Been doing this for years.
New Study shows virus 'likely infects gastrointestinal tissue' with 1 in 20 mild to moderate cases found to be pooping out virus nearly a year after infection:
So, is this WASTEWATER increase really proportional to the number of people who are infected?
Or are more people shedding the virus in their feces for longer?
I've been wondering about the modifications done to the mRNA in the vaccine. As has been pointed out several times, the dose of the actual spike protein given in the vaccine is indirect. You get a quantified dose of mRNA which must be translated into spike inside the cells.
Could another potential wild card in spike protein dose come from the way the mRNA was modified for vaccine production. Granted, stability is a problem with mRNA. I used to do a LOT of northern blots and other RNA work. It is very hard to work with. You look at the test tube sideways and it degrades.
The vaccines synthesized the mRNA for spike using a uridine analog to stabilize the structure. These analogs are common in structural RNA such as rRNA, but as far as my understanding goes, not found in mRNA. There is also a modified 5' CAP which increases translation and better prevents exonuclease activity. There are also several other modifications all geared to increase translation or prevent nuclease activity. (Kozak sequences, GC enriched sequences, and codon optimization). The Pfizer/BioNTech vaccine seems to have the highest number of these elements.
Anyway, what I find worrying is that the eukaryotic translation system has been optimized for over 2 billion years (give or take a few 100 million) to work with a very labile mRNA. So, they juiced this system up to compensate for mRNA instability. But how far is too far? After all the whole system has evolved to its present form as optimized for very short lived, unstable mRNA. Could this create unintended consequences with respect to total spike protein dose?
How variable is the amount of spike protein synthesized in vivo? Are a few people getting way too much? Others too little? What about the implications for an autoimmune response? haven't seen that much about how MUCH spike protein is being made and how variable it is across the population.
Maybe I'm making a big deal out of nothing. But everything seems to be modified in one direction which is increasing spike protein production. How heavy is the finger on that scale?
At his acceptance speech i hope he corrects his use of the word "timeless" when he should be saying "timely". Maybe that is a South African english quirk?
Thanks for such a outstanding discussion absolutely astonishing what Dr Chetty did for his patients and patient care
Dr McM. Thank you for posting this very very important piece.
Dr Chetty another outstanding physician.
Horrifying that the SA medical journal ignored his life saving paper.
What a massive exposure of the injection fraud too.
Any implications & possible help to your long covid reasearch?
Glad Dr Chetty getting some attention here.
Hello, Dr. McMillan! Great to meet you and this is fantastic!
Do you have another link to the interview, because youtube has taken it down.
Note: I came to this via Dr. Bryan Ardis, who has been saying since early on that venom is a part of this pandemic.
Thank you.
The beginning of the implementation of "their" plan to KILL HCQ AND STEROIDS etc, to kill early covid treatment and effective emergency room (as Dr Chetty's protocols) and hospital covid treatment, to push remdesivir and the vaccine only path is documented here https://apps.who.int/iris/bitstream/handle/10665/330680/WHO-HEO-RDBlueprint%28nCoV%29-2020.1-eng.pdf?sequence=1 WHO R&D Blueprint Informal consultation on prioritization of candidate therapeutic agents for use in novel coronavirus 2019 infection Geneva, Switzerland, 24 January 2020 - Coronavirus Outline of designs for experimental vaccines and therapeutics Draft version Jan 27, 2020
They "KILLED" steroids while the document acknowledges "although there is evidence of efficacy in the setting of severe illness".
The US representative at this Jan 2020 meeting was fauci stand in Hilary Marston - Medical Officer and Policy Advisor National Institute of Allergy and Infectious Diseases" with a big pharma "fixer" "McKinsey & Company and .. Bill & Melinda Gates Foundation" employment background.
Piercing insights with the character to say it. I call you friend always there.
Another Great video.
I've been a huge fan of both of you and Dr. Shankara Chetty. I remember when he was treating his patient's, who had to walk for miles and miles, outside his clinic in a tent. All the while mercenaries were robbing and burning down all the HCQ. Sending my sincerest appreciation. Thank you both very, very much. PS I was researching medicinal Artemisia in the O Chem lab at the time. I grow a species of it : ) and give it away. Been doing this for years.
It has been removed from youtube, where can we watch now pls?
New Study shows virus 'likely infects gastrointestinal tissue' with 1 in 20 mild to moderate cases found to be pooping out virus nearly a year after infection:
So, is this WASTEWATER increase really proportional to the number of people who are infected?
Or are more people shedding the virus in their feces for longer?
Chris Turnbull
https://twitter.com/EnemyInAState/status/1516806687897931777
THE STUDY ⬇️
Gastrointestinal symptoms and fecal shedding of SARS-CoV-2 RNA suggest prolonged gastrointestinal infection
https://www.cell.com/med/pdf/S2666-6340(22)00167-2.pdf
PDF ⬇️
https://www.cell.com/med/pdf/S2666-6340(22)00167-2.pdf
I've been wondering about the modifications done to the mRNA in the vaccine. As has been pointed out several times, the dose of the actual spike protein given in the vaccine is indirect. You get a quantified dose of mRNA which must be translated into spike inside the cells.
Could another potential wild card in spike protein dose come from the way the mRNA was modified for vaccine production. Granted, stability is a problem with mRNA. I used to do a LOT of northern blots and other RNA work. It is very hard to work with. You look at the test tube sideways and it degrades.
The vaccines synthesized the mRNA for spike using a uridine analog to stabilize the structure. These analogs are common in structural RNA such as rRNA, but as far as my understanding goes, not found in mRNA. There is also a modified 5' CAP which increases translation and better prevents exonuclease activity. There are also several other modifications all geared to increase translation or prevent nuclease activity. (Kozak sequences, GC enriched sequences, and codon optimization). The Pfizer/BioNTech vaccine seems to have the highest number of these elements.
Anyway, what I find worrying is that the eukaryotic translation system has been optimized for over 2 billion years (give or take a few 100 million) to work with a very labile mRNA. So, they juiced this system up to compensate for mRNA instability. But how far is too far? After all the whole system has evolved to its present form as optimized for very short lived, unstable mRNA. Could this create unintended consequences with respect to total spike protein dose?
How variable is the amount of spike protein synthesized in vivo? Are a few people getting way too much? Others too little? What about the implications for an autoimmune response? haven't seen that much about how MUCH spike protein is being made and how variable it is across the population.
Maybe I'm making a big deal out of nothing. But everything seems to be modified in one direction which is increasing spike protein production. How heavy is the finger on that scale?
How can we nominate Dr.Chetty for a Nobel Prize?
At his acceptance speech i hope he corrects his use of the word "timeless" when he should be saying "timely". Maybe that is a South African english quirk?