Post by sandokhan on Jun 1, 2023 7:01:25 GMT -5
Sars is M. avium, a mycobacterium. It uses several cellular receptors such as ACE2, DPP4 (the receptor of Mers-Cov) and HSPA5 (heat shock protein). Mers is M. influenzae. There are several passenger pathogens which go along with Sars: mycoplasma pneumoniae and chlamydia pneumoniae. Sars is treated with antibiotics: clarythromycin, since it is a mycobacterium and not/never a virus. There are no viruses, only mycobacteria and mycoplasma. HIV is also a mycobacterium, a variant of M. avium. So is poxviridae, a variant of M. leprae. The only vaccine which would have put a stop to Covid-19 would have been BCG with bacteriophages (without HeLa cells being used). Had clarythromycin been administered widely, it would have put an end to Sars(Cov-2) back in February 2020. There is also solithromycin, a fourth generation macrolide, and to a lesser degree azithromycin.
Most researchers think that "coronavirus" spike proteins had been discovered back in the 1960s. Not true. Spike proteins had been researched and discovered some 100 years ago by Wilhelm Reich. He called them T-bacilli. He even drew diagrams showing the spikes as they extend out of cells. Spike proteins are beta sheet prions, they absorb oxygen and vitality, hence the symptoms of hypoxia. There are also beneficial spike proteins, alpha helix prions.
The 1918 pandemic had started back in 1910, with the meteor showers from comet Halley. Then a huge pandemic had broken out in China in 1910-1911. Chinese workers then brought the pathogen to Europe (WWI). Then, a "coronavirus" pandemic spread worldwide in 1915-1917 (it was actually M. avium). Consequently, M. avium became M. influenzae in 1918, and finally became M. bovis with the eruption of the Katla volcano (12 October, 1918). Mers-Cov = H1N1 = M. influenzae. M. bovis/M. africanum = galloping tuberculosis.
Sars-Cov-2 has an astrobiological source, the meteor showers of the Beta Taurids (June-August; thus we can explain the summer waves, which otherwise would have no possible explanation) and of the Taurids (September-December).
Kurt Blome had discovered in the 1930s that bacteria communicate through radio waves (he also had discovered the HeLa cells technology which was brought to the US in the 1950s). L. Montagnier, a Nobel prize winner, confirmed these results in 2009. Bacteria can send electromagnetic copies of their cells over huge distances, instantaneously, using biological quantum entanglement through radio waves. This is how the new variants appeared worldwide, without any travel history. In March of 2020, the Wuhan strain was replaced in just two weeks by D614G, while the R0 factor could not be used to even vaguely explain this fact. Using the antenna and amplifier provided by the HeLa cells (AZ and J&J vaccines) and spike proteins (liquid crystals, Pfi/Mod) the bacteria in the labs and in the vaccinees was used to create the new variants which then were promptly transmitted to the mycobacterium in the atmosphere, that is why the masks were utterly useless, since the primary mode of transmission was atmosphere-person.
The Sars-Cov-2 genome has four nucleobases, so we are told. However, the cmRNA vaccines (chemically modified RNA also known as modRNA) have three nucleobases and one nucleoside (Uracil was substituted with Pseudouridine, an isomer of Uridine). Thus all of the resulting antibodies will be isomeric as well (isomeric abs were discovered back in 1994), mostly of the IgG4 format (IgD also plays a role). That is, the genetic code of the vaccines has nothing to do with the pathogen Sars-Cov-2. Delta was caused by two lethal antibodies: REGN10987 and B38. Here is the mechanism of the cmRNA vaccines: by sabotaging the immune system to produce a huge number of isomeric antibodies, the normal abs will be fabricated to a lesser degree (among which we count the two lethal abs which were described above). However, now the vaccinees have these isomeric abs in their organisms.
The genome of Sars-Cov-2 is 50% Mers-Cov: Omicron is Mers-Cov-2. It has been programmed to deactivate its prion domain (which was active in Delta) for some 18 months. The Deltacron variants = Sars-Cov-1. Thus, we can expect a M. influenzae outbreak (M. influenzae = H5N1 = Mers-Cov) after Omicron reactivates its prion domain. If there are several major volcanic eruptions, M. influenzae will become M. bovis, just like in 1918. There were also several lab experiments performed in the past years with anthrax/poxviridae and the spike protein from Sars-Cov-2. MPV has common genome with Sars-Cov-2/Omicron and is the catalyst which will reactivate the prion domain of Omicron.
Certainly there are pathogens present all the time in the atmosphere, but it is only in the late fall of 2019 that Sars-Cov-2 was detected. What, then, had caused the volume of mycobacterium in the atmosphere to increase greatly? This can only happen at the end of a geological/astronomical age/epoch, when there will be two phenomena to deal with: the reversal of the magnetic poles and then a shift of the stellar dome (geocentrism) or a shift of the geographical poles (heliocentrism).
Most researchers think that "coronavirus" spike proteins had been discovered back in the 1960s. Not true. Spike proteins had been researched and discovered some 100 years ago by Wilhelm Reich. He called them T-bacilli. He even drew diagrams showing the spikes as they extend out of cells. Spike proteins are beta sheet prions, they absorb oxygen and vitality, hence the symptoms of hypoxia. There are also beneficial spike proteins, alpha helix prions.
The 1918 pandemic had started back in 1910, with the meteor showers from comet Halley. Then a huge pandemic had broken out in China in 1910-1911. Chinese workers then brought the pathogen to Europe (WWI). Then, a "coronavirus" pandemic spread worldwide in 1915-1917 (it was actually M. avium). Consequently, M. avium became M. influenzae in 1918, and finally became M. bovis with the eruption of the Katla volcano (12 October, 1918). Mers-Cov = H1N1 = M. influenzae. M. bovis/M. africanum = galloping tuberculosis.
Sars-Cov-2 has an astrobiological source, the meteor showers of the Beta Taurids (June-August; thus we can explain the summer waves, which otherwise would have no possible explanation) and of the Taurids (September-December).
Kurt Blome had discovered in the 1930s that bacteria communicate through radio waves (he also had discovered the HeLa cells technology which was brought to the US in the 1950s). L. Montagnier, a Nobel prize winner, confirmed these results in 2009. Bacteria can send electromagnetic copies of their cells over huge distances, instantaneously, using biological quantum entanglement through radio waves. This is how the new variants appeared worldwide, without any travel history. In March of 2020, the Wuhan strain was replaced in just two weeks by D614G, while the R0 factor could not be used to even vaguely explain this fact. Using the antenna and amplifier provided by the HeLa cells (AZ and J&J vaccines) and spike proteins (liquid crystals, Pfi/Mod) the bacteria in the labs and in the vaccinees was used to create the new variants which then were promptly transmitted to the mycobacterium in the atmosphere, that is why the masks were utterly useless, since the primary mode of transmission was atmosphere-person.
The Sars-Cov-2 genome has four nucleobases, so we are told. However, the cmRNA vaccines (chemically modified RNA also known as modRNA) have three nucleobases and one nucleoside (Uracil was substituted with Pseudouridine, an isomer of Uridine). Thus all of the resulting antibodies will be isomeric as well (isomeric abs were discovered back in 1994), mostly of the IgG4 format (IgD also plays a role). That is, the genetic code of the vaccines has nothing to do with the pathogen Sars-Cov-2. Delta was caused by two lethal antibodies: REGN10987 and B38. Here is the mechanism of the cmRNA vaccines: by sabotaging the immune system to produce a huge number of isomeric antibodies, the normal abs will be fabricated to a lesser degree (among which we count the two lethal abs which were described above). However, now the vaccinees have these isomeric abs in their organisms.
The genome of Sars-Cov-2 is 50% Mers-Cov: Omicron is Mers-Cov-2. It has been programmed to deactivate its prion domain (which was active in Delta) for some 18 months. The Deltacron variants = Sars-Cov-1. Thus, we can expect a M. influenzae outbreak (M. influenzae = H5N1 = Mers-Cov) after Omicron reactivates its prion domain. If there are several major volcanic eruptions, M. influenzae will become M. bovis, just like in 1918. There were also several lab experiments performed in the past years with anthrax/poxviridae and the spike protein from Sars-Cov-2. MPV has common genome with Sars-Cov-2/Omicron and is the catalyst which will reactivate the prion domain of Omicron.
Certainly there are pathogens present all the time in the atmosphere, but it is only in the late fall of 2019 that Sars-Cov-2 was detected. What, then, had caused the volume of mycobacterium in the atmosphere to increase greatly? This can only happen at the end of a geological/astronomical age/epoch, when there will be two phenomena to deal with: the reversal of the magnetic poles and then a shift of the stellar dome (geocentrism) or a shift of the geographical poles (heliocentrism).