Assassinated: The Russian General who Exposed US Biolabs in Ukraine.
Plus a Further Avalanche of Medical News; December 18, 2024.
You may have read in the news yesterday that Ukrainian forces have assassinated Russian Lt. General Igor Kirilov outside his Moscow apartment building. The Ukrainian government is publicly taking credit for the killing, so there is no mystery about it.
What you may not know is that Gen. Kirilov is the man who has been reporting on investigations into Ukraine/US biolabs containing a large array of potentially lethal pathogens, which Russian forces have found scattered across Ukraine.
It is very worth watching this 2min19sec video referenced in the image above.
International news analyst Pepe Escobar: ‘‘Lt Gen Kirillov was assassinated by the CIA/SBU - on behalf of Big Pharma - because he and his team connected all the dots. All the data is in the possession of the UN, which won't do anything about it.”
You may or may not recall that in March, 2023, Gen. Kirilov published the following chart:
Here is the Russian version:
And here is yesterday’s news coverage from the US site, ZeroHedge:
2. Disease X is Malaria—probably.
Perhaps you have read in the news about a new disease outbreak in Africa that some are calling "Disease X"? Well, here it is.
When will this ever end?
"Congo's Health Ministry Confirms 'Disease X' is Malaria
Outbreak began shortly after Congo's rollout of the novel R21 virus-like particle malaria vaccine."
Nicholas Hulscher, MPH: “Right before this malaria outbreak began, in late October, the Congo introduced the novel R21 malaria vaccine into their national immunization program. “R21 is a virus-like particle comprising the central repeats of Asn-Ala-Asn-Pro (NANP) and C-terminal sequence of circumsporozoite protein fused to the hepatitis B surface antigen (HBsAg).” It would not be surprising if this new vaccine played a significant role in triggering or exacerbating the severe malaria outbreak.”
Will continue to follow.
3. Children vaccinated with Pfizer-BioNTech without prior SARS-CoV-2 infection were 159% more likely to get infected and 257% more likely to develop symptomatic COVID-19 compared to unvaccinated children without prior infection.
The study link is here, also on Dr. McCollough’s blog, along with commentary by Nicholas Hulscher.
4. Looks like dose 4 of Pfizer is the worst for breakthrough infections (BT) but they are all bad.
Jessica Rose, Ph.D., posted this preliminary report on her blog; a formal published study is planned to follow.
“The highest percentage of dose-specific BT (breakthrough Covid infections) reports of total BT reports is seen following dose 4 (30%), followed by dose 3 (16%) and doses 1 and 2 (4% and 12%, respectively).
Dr. Rose theorizes that the reason for increased susceptibility to new versions of the SARS Cov-2 virus involves the immune system progressively switching to a type of antibody, called IGG-4, which induces tolerance to invading virus.
Upshot: Don’t get it!
P.S. Isn’t SUBSTACK wonderful?
5. How Covid was Constructed? A Clue.
Intrepid researcher Billy Bostickson (the name is apparently a pseudonym; Bostickson was an original member of D.R.A.S.T.I.C., a loose collection of researchers who were among the first to question the idea of a zoonotic origin of Covid-19) has uncovered scientific papers which indicate the SARS Cov-2 (Covid-19) could be the product of a recombination event in a lab.
A bat coronavirus, which is not very infective for humans, may have acquired a FURIN CLEAVAGE SITE (FCS) from another laboratory sample of pangolin coronavirus, which does contain the furin cleavage site. It is the furin cleavage site that makes SARS Cov-2 so infectious for humans.
Bostickson’s argument:
It is well-known that the Wuhan Lab was experimenting with many types of bat coronaviruses. One of those bat coronaviruses, called RaTG13, I believe, a 97% resemblance to SARS Cov-2.
It is the furin cleavage site on SARS Cov-2 that allows it to effectively attach to the ACE-2 receptor on human cells and so cause the infection that we call Covid-19.
No bat coronavirus has been found so far that contains an efficient furin cleavage site for human infection.
But it turns out that a MALAYSIAN GOLDEN PANGOLIN variety of coronavirus does contain such a site.
Bostickson:
“It is not yet known how SARS-COV-2 acquired its FCS.
“Propagation of the progenitor of SARS-CoV-2 (e.g. RaTG13) together with a MERS-CoV is likely to lead to the selection of a virus that gains functions of both viruses, thus increasing its infection rate in vitro.
“MjHKU4r-CoV-1 Spike (from pangolin coronavirus) is processed by furin 4. FCS enhances viral entry into human cells by 2–3 orders of magnitude compared to bat HKU4 5. Thus, MjHKU4r-CoV-1 Spike has acquired a functioning FCS that confers entry into human cells.
“A Logical Chain & Evidence have now been found.
“What remains is the question of the exact pathway and experiments that that led to the acquisition of an FCS in Sars-COV-2 in the laboratories of the WIV.
“Now for a "Very Big" Statement in Nature!
"However, a virus related to pangolin-CoV appears to have donated the RBD to SARS-CoV-2"
(Xiao et al., 2020) Received 16 Feb 2020
Isolation of SARS-CoV-2-related coronavirus from Malayan pangolins
Isolation of SARS-CoV-2-related coronavirus from Malayan pangolins - NatureA newly identified coronavirus found in Malayan pangolins shares considerable sequence identity with SARS-CoV-2, which suggests that the latter may have originated from a recombination event involving…https://www.nature.com/articles/s41586-020-2313-x
Bostickson’s thread implies that SARS COV-2 may have acquired its FCS via cell culture contamination involving GX Pangolin MERS Cov isolates (MjHKU4r-CoV-1) stored & experimented on at WIV in 2019.
This supports the hypothesis that the PCS/furin cleavage site was gained by a recombination event involving these virus sequences.
Mr. Bostickson seems to think the recombination event was a lab accident. I don’t know why he thinks this was an accident. He does not say, in this long and convoluted X thread which he posted on December 12:
You can follow the X post on THREADREADER, here:
https://threadreaderapp.com/thread/1867180342597341532.html
6. We Could not Have a Better Champion for Vaccine Safety.
7.
My Christmas prayer for everyone:
Keep speaking, keep learning, keep singing, keep shining.
Best wishes,
Haru
If you haven’t checked out my other SUBSTACK site, I would like to invite you to do so. My most recent post discusses the Molecular Theory of Cancer.
Many good subjects and leads in this one and I have not chased through all of them.
About the Pangolin Connection: Pangolin was "used as an excuse" during the original SARS incident. I have not read about its role in the SARS-Covid-2 before this point. however, it has been widely rumored that the 3 incidents were actually inter-connected in the sense of systematic trial-by-error to improve both the infection tendency AND the lethality. Personally I don't have the knowledge to provide a scientific opinion. The "furin cleavage site" had been discussed and debated since the early days. My own "conclusion" after reading multiple articles is the whole thing is a genetic-engineering product starting from a bat virus (which provided 97-98% of the RNA materials) AND the developed virus was intentionally passed through multiple in-lab propagation to "smooth out its edges" by adding some random speckles to the less important segments of the RNA. IMHO, the futuristic "Disease X" is more likely to be a positively-sensed ssRNA virus, fast-cloning and fast-mutating, never an effective vaccine possible. But the great medical world most likely will push all of us into that endless chase. It is the improvement in basic human immunity for the basic defense lines, plus some Rx to deal with the symptoms.