Despite my twitter suspension, Bot has managed to get over 100 retweets on this, almost 15k impressions and 1k engagements. Keep on going and thanks for spreading the word
https://twitter.com/robinmonottibot/status/1369989678582095873?s=19

There is a potential explanation for the very wide range of outcomes after vaccination, with the majority suffering no ill effects, some getting adverse effects & a small number dying.
If we are correct that it’s expression of spike protein that drives pathology - and this would tally with the range of thromboembolic responses in SARS-CoV-2 infection - then it has to be recognised that the absolute level of expression is likely to vary greatly. This is because the distribution of the material will vary, so will uptake, so will translation / transcription, then factor is a wide range of sensitivity to spike protein as well.
My original training included toxicology & the focus was on molecular mechanisms of toxicity.
This might all be wrong, but it does fit & so is a candidate explanation, to be investigated / disproven / supported.

"Any finding on yellow card data gets dismissed because no-one knows what the true denominator is or if everything gets reported.

But you can compare the two vaccines. If they were harmless results would be identical. AZ has a mortality rate 34% >Pfizer."
https://twitter.com/ClareCraigPath/status/1370007605205229569?s=19
https://t.co/8jX9BQ8fHi

The mortality is higher with AZ than with Pfizer. Moderna?

With news of new restrictions being imposed in Italy, this confirms what I explained in my interview with Geopolitics & Empire: the real reason for lockdown is the roll-out of central bank digital currencies as a replacement for cash. Mario Draghi is the former ECB President, he will be the first to push anything that will eliminate cash. At the same time, the ICMRA requires minimum one year of safety studies on vaccines before any national regulatory body can approve them. If restrictions are lifted, and precisely because they are causing serious adverse events, then the temporary authorisation for the vaccines, either for emergency use (US) or marketing licenses (EU) can be revoked with a legal action. Therefore it is imperative to the pharmaceutical companies that some restrictions stay in place until June 21st. At the same time it gives a large enough window during which pressure will be exerted to take the vaccines. For the AZ vx, they will blame a faulty batch rather than the design, but the damage to the image of the AZ vx is done and irreversible no matter how hard they try and revive it. We know it was not a faulty batch but the S spike protein in the vaccines that can damage healthy people. See next post.
https://www.youtube.com/watch?v=YOp3oY6cUts

https://www.patreon.com/robinmonotti

Patrick Whelan MD PhD:"I am concerned about the possibility that the new vaccines aimed at creating immunity against the SARS-CoV-2 spike protein (including the mRNA vaccines of Moderna and Pfizer) have the potential to cause microvascular injury to the brain, heart, liver, and kidneys in a way that does not currently appear to be assessed in safety trials of these potential drugs...it appears that the viral spike protein that is the target of the major SARS-CoV-2 vaccines is also one of the key agents causing the damage to distant organs that may include the brain, heart, lung, and kidney. Before any of these vaccines are approved for widespread use in humans, it is important to assess in vaccinated subjects the effects of vaccination on the heart (perhaps using cardiac MRI, as Puntmann et al. did). Vaccinated patients could also be tested for distant tissue damage in deltoid area skin biopsies, as employed by Magro et al. As important as it is to quickly arrest the spread of the virus by immunizing the population, it would be vastly worse if hundreds of millions of people were to suffer long-lasting or even permanent damage to their brain or heart microvasculature as a result of failing to appreciate in the short-term an unintended effect of full-length spike protein-based vaccines on these other organs.

Particular caution will be required with regard to the potential widespread vaccination of children before there are any real data on the safety or effectiveness of these vaccines in pediatric trials that are only now beginning."
Regulations.gov
https://www.regulations.gov/document/FDA-2020-N-1898-0246

Doctors & Scientists Write to European Medicines Agency Warning of COVID-19 Vaccine Dangers



https://wp.me/paXmj6-jft

Doctors and Scientists Challenge European Medicines Agency on COVID-19 Vaccine Danger

https://21stcenturywire.com/2021/03/11/doctors-and-scientists-challenge-european-medicines-agency-warning-of-covid-19-vaccine-dangers/

This briefing has been produced ahead of the debate to be held in Westminster Hall on Monday 15 March 2021 at 4.30 pm on e-petition 569957 (Covid-19 vaccine passports).
DEBATE PACK
Number CDP 2021-0038 , 11 March 2021
Debate on an e-petition
relating to Covid-19
vaccine passports

CDP-2021-0038.pdf

VITAMIN D ☀️.
Download this app on your mobile: dminder
"Wherever you go in the world, dminder tracks the sun and tells you when you can get Vitamin D. The stopwatch interface lets you set your session target by either amount of D to get or time. Then it will count up or down to your target, applying all the factors that determine how much D you can get: skin tone, age, weight, amount of skin exposed. All your doses of D, from the sun or supplements, are used to continuously estimate your current level. Developed with world authority on Vitamin D, Dr. Michael Holick."
http://dminder.ontometrics.com/

I now listened to this pathologist, Dr Ryan Cole, who explains very clearly points 2 (vitamin D) and 3 (early treatment) of the Monotti Protocol. All you need to listen to are the first 25 minutes. https://youtu.be/oA-fTaGadyc

Gut bacteria and vitamin D: What is the link?

"We were surprised to find that microbiome diversity — the variety of bacteria types in a person’s gut — was closely associated with active vitamin D but not the precursor form,” says senior author of the study Dr. Deborah Kado, director of the Osteoporosis Clinic at UC San Diego Health.
“Greater gut microbiome diversity is thought to be associated with better health in general,” she adds.

https://www.medicalnewstoday.com/articles/gut-bacteria-and-vitamin-d-what-is-the-link#Stores-of-inactive-vitamin-D

"The email identified “a significant difference in % RNA integrity/truncated species” between the clinical batches and proposed commercial batches—from around 78% to 55%. The root cause was unknown and the impact of this loss of RNA integrity on safety and efficacy of the vaccine was “yet to be defined,” the email said.

One of the most important variables relevant to all mRNA vaccines that has thus far received scant attention in the clinical community. It is an issue relevant not just to Pfizer-BioNTech’s vaccine but also to those produced by Moderna, CureVac, and others ,4 as well as a “second generation” mRNA vaccine being pursued by Imperial College London.5
RNA instability is one of the biggest hurdles for researchers developing nucleic acid based vaccines. It is the primary reason for the technology’s stringent cold chain requirements and has been addressed by encapsulating the mRNA in lipid nanoparticles (box).
“The complete, intact mRNA molecule is essential to its potency as a vaccine,” professor of biopharmaceutics Daan J.A. Crommelin and colleagues wrote in a review article in The Journal of Pharmaceutical Sciences late last year. “Even a minor degradation reaction, anywhere along a mRNA strand, can severely slow or stop proper translation performance of that strand and thus result in the incomplete expression of the target antigen.”

The Medicines and Healthcare products Regulatory Agency, the UK’s medicines regulator, acknowledged the lack of a specified percentage RNA integrity, but declined to provide further detail. “The specification limit acceptance criteria are commercially confidential,” the agency said in an email.

https://www.bmj.com/content/372/bmj.n627