Excellent work! Yes, we are in the middle of an ‘experiment in nature’ where we are the subjects (guinea pigs). It seems to me that the mechanisms you describe here could all fall under the heading of “Unintended Consequences of Unleashing Untested Vaccines.”
"....In order to propagate for example viral SARS-CoV-2 infection with a big pool of identical building blocks common with HIV-1, with Marburg, with all the other viruses mentioned in previous posts, incredible large portions of HUMAN proteins, any genetic re-programming of the human body for synthetic SARS Spikes production will automatically affect infections with other even more lethal or maybe even benign viruses."
On to bacteria....
And, now, I am so happy to be able to share your Substack research on bacteria with two io groups.
We know that the virus can enter bacteria and stick around for a long period. Further, a most intriguing finding, Different lineages? Hijacking of the cellular machinery of two different species? "Overall, this finding provides an indication that bacteria might be a potential source of novel SARS mutations, and gives rise to the possibility that intra-host SARS haploytpes might reflect different intestinal bacterial prior host environments of the virus. This observation would represent the basis for one of the proposed origins of the Omicron variant i.e. that Omicron (and other variants) might have evolved in the gut bacteria of one person."
Wow! This is incredible research. Thank you for your diligence and thoroughness. I was always intrigued by the Pradhan paper on finding gp120 in Sars-Cov-2. Is it possible that SARS-2 can use gp120 as an envelope to gain entry to CD4 cells like HIV by creating HVP? It’s intriguing especially when you consider the Spike protein tests HIV positive. What does this all mean? We have opened Pandoras Box. God help us!
if they were to do a proper biodistribution study of the transfection, it would seem prudent to also look at the microbiome, perhaps with stool and urine, in a way that captures all the stuff from something like a genova diagnostics ION or Metabolomix panel.
OK, lets see if I understand your last few articles:
So, C19 virus can also interact or mess with bacteria? So, C19 is a bit like NATO, it interacts with western democracies but also brings along nazis for the ride. And the spike is like a tank, it pierces membranes and tramples everywhere and LPS endotoxin hitches along for the ride, after the tank breaks into a cell, out bursts all the LPS toxic soldiers with AK47's to cause havoc?
Great! It appears that fenbendazole exploits a common weakness (within the microtubule system) that most cancer cells share. This selective attack on the cancer cell is very targeted which is why fenbendazole is free of side effects.
Off topic slightly, but I read somewhere that a paper showed all the mice died after 9-15 exposures to spike. I was wondering if that sort of thing was true and I know mouse studies are good but I also know mice biology is different to human. Maybe if it takes 9 exposures to kill all the mice itll take 109 exposures to kill a human or1009.
So far I think Ive only been exposed once. In December 2019 I had a long flu for about 2 weeks and ever since I have constant green plegm in my throat, especially upon waking. It may have been flu and not covid.
Excellent work! Yes, we are in the middle of an ‘experiment in nature’ where we are the subjects (guinea pigs). It seems to me that the mechanisms you describe here could all fall under the heading of “Unintended Consequences of Unleashing Untested Vaccines.”
Thank you so much for compiling and sharing such fascinating information!!!
Just yesterday, I learned about common building blocks of SARS with other viruses on the absolutely wonderful mejbcart Substack cited below:
https://mejbcart.substack.com/p/how-much-hiv-is-in-sars-cov-2-faucis
"....In order to propagate for example viral SARS-CoV-2 infection with a big pool of identical building blocks common with HIV-1, with Marburg, with all the other viruses mentioned in previous posts, incredible large portions of HUMAN proteins, any genetic re-programming of the human body for synthetic SARS Spikes production will automatically affect infections with other even more lethal or maybe even benign viruses."
On to bacteria....
And, now, I am so happy to be able to share your Substack research on bacteria with two io groups.
Carlo Brogna and his team have another cool study. https://f1000research.com/articles/11-292
We know that the virus can enter bacteria and stick around for a long period. Further, a most intriguing finding, Different lineages? Hijacking of the cellular machinery of two different species? "Overall, this finding provides an indication that bacteria might be a potential source of novel SARS mutations, and gives rise to the possibility that intra-host SARS haploytpes might reflect different intestinal bacterial prior host environments of the virus. This observation would represent the basis for one of the proposed origins of the Omicron variant i.e. that Omicron (and other variants) might have evolved in the gut bacteria of one person."
Wow! This is incredible research. Thank you for your diligence and thoroughness. I was always intrigued by the Pradhan paper on finding gp120 in Sars-Cov-2. Is it possible that SARS-2 can use gp120 as an envelope to gain entry to CD4 cells like HIV by creating HVP? It’s intriguing especially when you consider the Spike protein tests HIV positive. What does this all mean? We have opened Pandoras Box. God help us!
Thanks for putting words and sense to the thoughts that have been roaming through my mind. Well done. It’s nice to know we aren’t just crazy people.
if they were to do a proper biodistribution study of the transfection, it would seem prudent to also look at the microbiome, perhaps with stool and urine, in a way that captures all the stuff from something like a genova diagnostics ION or Metabolomix panel.
I’d be curious on your take on this unique observation regarding fenbendazole and cancer. As the covid vax ramps up cancer incidence in its victims fenbendazole, as an ORC, safe and cheap cancer treatment is timely https://fenbendazole.substack.com/?r=oh1g6&utm_campaign=pub&utm_medium=web
OK, lets see if I understand your last few articles:
So, C19 virus can also interact or mess with bacteria? So, C19 is a bit like NATO, it interacts with western democracies but also brings along nazis for the ride. And the spike is like a tank, it pierces membranes and tramples everywhere and LPS endotoxin hitches along for the ride, after the tank breaks into a cell, out bursts all the LPS toxic soldiers with AK47's to cause havoc?
i've been trying to wrap my head around the significance of this, because this seems to have huge implications, if i'm understanding this right...
it is possible then that the spike protein from SARS-CoV-2 can incorporate itself into other viruses?
if this is the case, would the spike protein inside a different virus go undetected during testing for SARS-CoV-2 exposure?
Great! It appears that fenbendazole exploits a common weakness (within the microtubule system) that most cancer cells share. This selective attack on the cancer cell is very targeted which is why fenbendazole is free of side effects.
Off topic slightly, but I read somewhere that a paper showed all the mice died after 9-15 exposures to spike. I was wondering if that sort of thing was true and I know mouse studies are good but I also know mice biology is different to human. Maybe if it takes 9 exposures to kill all the mice itll take 109 exposures to kill a human or1009.
So far I think Ive only been exposed once. In December 2019 I had a long flu for about 2 weeks and ever since I have constant green plegm in my throat, especially upon waking. It may have been flu and not covid.