Stephan Bernstein, CEO of GreenRoc, details the PFS results for the new graphite processing plant. Watch the video here.
It is actually only by complete fluke that the sniffys have seen an uptick in the shares.
It is solely down to covidity.
The rest has been hot air for over a decade.
Which makes the sniffys even more irritating as they invested in all the other stuff and are still claiming moral high ground
part 3
I, therefore, reiterate that the currently observed convergence of naturally selected mutations towards S-derived antigenic sites that facilitate or are directly responsible for binding to the Ace-2 entry receptor combind with the velocity at which this evolution currently takes place poses a huge and imminent threat to the human population and will heavily backfire if we continue mass vaccination on a background of high viral infection rates while largely relaxing infection prevention measures.
Last but not least, it must be emphasized that those calling themselves ‘experts’ while pretending that this pandemic is ‘a pandemic among the non-vaccinated’ are devoid of any scientific insight in the evolutionary dynamics of Sars-CoV-2 as currently shaped by a combination of high viral infectivity and vaccine coverage rates. Neither the vaccinated (who merely believed the vaccine would protect them from Covid-19 disease) nor the non-vaccinated (who simply believe there is no need for them to take the vaccine in order to stay protected) are to be blamed for the escalation of this pandemic. Mass vaccination is the one and only culprit.
Note: A copy of this letter has been sent to WHO, NIH, CDC, the Bill & Melinda Gates Foundation, GAVI, CEPI, FDA, EMEA and to R&D leaders from Pfizer, Moderna, Astra-Zeneca, J&J, Novavax and GSK
It is quite most on here have no idea what they are invested in and even less about the pandemic.
The sniffy old guard are a joke having spent 9 years in purgatory they have become blinded to reality.
Part 2
Overall Conclusion
Both, long-lived Sars-CoV-specific immunity acquired upon recovery from disease and innate, CoV-nonspecific Ab-mediated immunity normally contribute to establishing broadly protective herd immunity and thereby enable a natural CoV pandemic (or, for that matter, any pandemic of an acute, self-limiting viral disease) to eventually transition into an endemic phase. However, circulation of more infectious variants comes with a high price to pay for herd immunity to establish as high infectivity rates are more likely to erode natural, polyreactive (i.e., CoV-nonspecific) immunity in young and/ or healthy individuals. As a result, morbidity and hospitalization rates, and ultimately also the number of deaths, will increase. This self-amplifying cycle of enhanced viral infectiousness (resulting in enhanced viral infectivity rates) would only come to an end when the population density is diluted down to a level low enough for viral transmission (of a highly transmissible/ infectious variant!) to substantially diminish.
Whereas fast and dominant propagation of naturally selected, more infectious variants continues to erode the natural first line of variant-nonspecific immune defense in the non-vaccinated part of the population, vaccination of large parts of the population and contacts among vaccinated and non-vaccinated subjects are driving natural selection and adaptation of increasingly VI-escaping variants and are, therefore, increasingly compromising VMI. Neither previous CoV infection (including Sars-CoV-2 infection), nor higher vaccine coverage rates can compensate for the lost immunological capacity. Indeed, memory T cells elicited upon previous CoV infection or vaccination are not reportedly known to be endowed with cytotoxic activity towards CoV-infected cells, nor can S-specific Abs elicited upon previous CoV infection or vaccination prevent spreading of more infectious Sars-CoV-2 variants. Molecular epidemiologists have suggested that immune failure to block viral transmission (e.g., in immunosuppressed patients) causes variants to convergently evolve specifically selected mutations, thereby enabling escape from VMI. VI escape together with suppression of natural, CoV-nonspecific Abs by vaccinal Abs will make vaccinees highly susceptible to contracting Covid-19 disease.
Dominant propagation of more infectious viral variants could be mitigated by mass chemoprophylaxis using a potent antiviral. At the same time, immune pressure on vaccinal S-specific epitopes must be mitigated by calling an immediate halt to mass vaccination campaigns. Furthermore, early treatment of symptomatic subjects can prevent severe disease and provide them with durable protection against a diversified spectrum of more infectious variants and, thereby, also reduce viral transmission. However, this is the last opportunity to limit the disastrous consequences of mass vaccination
A last word of caution to all those pretending the Covid-19 pandemic is toning down
https://www.geertvandenbossche.org/post/a-last-word-of-caution-to-all-those-pretending-the-covid-19-pandemic-is-toning-down
Synopsis
The current expansion in prevalence of infectious Sars-CoV-2 variants is highly problematic because it erodes natural Ab-based, variant-nonspecific immunity in the non-vaccinated part of the population. The high infectivity rate that results from this expansion not only further enhances the expansion of these variants but may also drive natural selection of viral variants that are featured by an even higher level of infectiousness. Erosion, therefore, of natural Ab-based, variant-nonspecific immunity promotes breeding and transmission of more infectious viral variants in the non-vaccinated part of the population. On the other hand, mass vaccination promotes natural selection of increasingly vaccine immunity (VI)-escaping variants in the vaccinated part of the population. Taken together, mass vaccination conducted on a background of high infectivity rates enables more infectious, increasingly VI-escaping variants to expand in prevalence. This evolution inevitably results in inclining morbidity rates in both, the non-vaccinated and vaccinated population and precipitates the emergence of circulating viral variants that will eventually fully resist vaccine-mediated immunity (VMI). This is why mass vaccination campaigns should not be conducted during a pandemic of a highly mutable virus, let alone during a pandemic of more infectious variants (unless transmission-blocking vaccines are used!). It is critical to understand that a rapid decline in viral infectivity rates that is not achieved by natural infection but merely results from expedited mass vaccination campaigns will only delay abrupt propagation of emerging, fully vaccine-resistant viral variants and hence, only delay the occurrence of a high wave of morbidity and mortality. In contrast, mass vaccination campaigns that are progressing more slowly, especially when conducted on a background of relatively low infectious pressure, will result in a steadily growing propagation of increasingly VI-escaping variants and hence, cause a wave of morbidity and mortality that continues to grow bigger and larger as more and more people become vaccinated. It’s only when fully vaccine-resistant viral variants will become dominant that this wave will start to peak.
To prevent more detrimental consequences of the ongoing evolution of Sars-CoV-2, we have no choice but to mitigate erosion of natural, Coronavirus (CoV)-nonspecific immunity in non-vaccinated individuals and exertion of strong immune selection pressure on immunodominant vaccinal epitopes in vaccinated individuals. This is to say that we must stop mass vaccination and lower viral infectivity rates immediately. Continued mass vaccination will only lead to a further increase in morbidity and hospitalization rates,
Luc Montagnier
Luc Montagnier is a French virologist and joint recipient, with Françoise Barré-Sinoussi and Harald zur Hausen, of the 2008 Nobel Prize in Physiology or Medicine for his discovery of the human immunodeficiency virus. He has worked as a researcher at the Pasteur Institute in Paris and as a full-time professor at Shanghai Jiao Tong University in China.
Montagnier said in part:
We’re in unknown territory and proclaim mandatory vaccines for everyone. It’s insanity. It’s vaccination insanity that I absolutely condemn.
He explained that he “is not looking for controversy, but for truth”.
Some of the points made in a clip of the interview translated exclusively for RAIR Foundation USA reveal that Prof. Montagnier is “outraged” that widespread vaccination of children could have horrific generational consequences.
He gives the example of the herbicide glyphosate, which can be passed on to future generations in a process known as “Transgenerational Epigenetic Inheritance.”
“Recent studies on glyphosate have shown that there are epigenetic effects,” Prof. Montagnier explained. “That means people who eat glyphosate in their diet pass on something that will affect future generations. Their children, their grandchildren, and great-grandchildren, they will suffer,” he continued.
The Nobel Laureate explained that the “Messenger RNA” may result in disastrous consequences without proper study. He said:
This Messenger RNA that’s being injected today in vaccines, may have effects on future generations that are undetected if we aren’t searching for them.
Another concern Montagnier expresses is the possibility of side effects of vaccines that could be seen in “five to ten years” related to “neurodegenerative illness.”
Neurodegenerative disease is “an umbrella term for a range of conditions which primarily affect the neurons in the human brain” and is described as “incurable and debilitating conditions that result in progressive degeneration and/or death of nerve cells.”
Montagnier states that there “are sequences that resemble the prion sequences in the RNA of the coronavirus” and could therefore “disorder the natural proteins in the brain, modifying them to make prions.”
A research article titled “RNA editing alterations define manifestation of prion diseases” explains that “Prion diseases are fatal neurodegenerative disorders characterized by rapidly progressive dementia.”
Anecdotal evidence,sure but President Biden's faculties have very significantly declined since he has been vaccinated.
To the point of is he fit to be the President?
https://www.youtube.com/watch?v=t7WwDLzG--Y
Deadly Prion Brain Diseases & Experimental mRNA Jabs
An important and highly concerning study published early this year in the journal Microbiology & Infectious Diseases titled, “Covid-19 RNA Based Vaccines and the Risk of Prion Diseases,” addresses one of the many potential, unintended, adverse health effects of the experimental mRNA Covid-19 vaccines presently being deployed worldwide, namely, their possible induction of prion diseases, a category of highly fatal brain disorders.
The study abstract, well worth reading, summarizes both the context, intention, and results of the investigation:
“Development of new vaccine technology has been plagued with problems in the past. The current RNA based SARSCoV-2 vaccines were approved in the US using an emergency order without extensive long term safety testing. In this paper the Pfizer COVID-19 vaccine was evaluated for the potential to induce prion-based disease in vaccine recipients.
The RNA sequence of the vaccine as well as the spike protein target interaction were analyzed for the potential to convert intracellular RNA binding proteins TAR DNA binding protein (TDP-43) and Fused in Sarcoma (FUS) into their pathologic prion conformations. The results indicate that the vaccine RNA has specific sequences that may induce TDP-43 and FUS to fold into their pathologic prion confirmations.
In the current analysis a total of sixteen UG tandem repeats (?G?G) were identified and additional UG (?G) rich sequences were identified. Two GG?A sequences were found. Potential G Quadruplex sequences are possibly present but a more sophisticated computer program is needed to verify these. Furthermore, the spike protein, created by the translation of the vaccine RNA, binds angiotensin converting enzyme 2 (ACE2), a zinc containing enzyme.
This interaction has the potential to increase intracellular zinc. Zinc ions have been shown to cause the transformation of TDP-43 to its pathologic prion configuration. The folding of TDP-43 and FUS into their pathologic prion confirmations is known to cause ALS, front temporal lobar degeneration, Alzheimer’s disease and other neurological degenerative diseases.
The enclosed finding as well as additional potential risks leads the author to believe that regulatory approval of the RNA based vaccines for SARS-CoV-2 was premature and that the vaccine may cause much more harm than benefit. [emphasis added]“
https://principia-scientific.com/deadly-prion-brain-diseases-experimental-mrna-jabs/
Nobody can say with any certainty what is going to happen.The human race has been put through a massive experiment.
Only time will tell.
The great concern by people like Nobel prize winning Luc Montagnier, who co discovered the HIV virus, with the MRNA vaccine is that it delivers spike proteins into the body.
From the freedom of infomation act obtained in Japan about the Pfizer vaccine,it appears that they knew it does not stay only at the injection sites
Spike protein have been found in ovaries and other organs,they are also able to pass the blood brain barrier.
The great unknown with these experimental vaccines is could they cause a Prion BSE type mad cow disease or other diseases
Two weeks in mice is 18 months in humans,so we will not know for another 8 months or so.
I detect this dreadful sniffiness by the old guard here.
Anyway the reality is Biontech only really started motoring with the development of is far from perfect first generation MRNA vaccine.
If Scancell's covidity does what it says on the tin,the incumbents could be toppled and the share price go up to 580 times higher.
Then there are all the other Scancell platforms.