Dr Burkhardt's team published more autopsy data on COVID π patients confirming lymphocytes in every organ; which means it's a good time to revisit this little gem of a paper, with many highly predictive statements about the LNPs in the #WarpedSpeed π>
Before we start it's interesting to note the paper is from a team at Thomas Jefferson University.
The same π« which forced their president to publicly apologize for liking @AlexBerenson's tweets questioning the safety and efficiency of the πs.
The research looked at data showing the highly inflammatory nature of the lipid nanoparticles when tested in π, injected into the muscle, and intranasally. > ncbi.nlm.nih.gov/pmc/articles/Pβ¦
Remember this fact about the PEG.
We'll come back to it later in the context of the #StringOfPearls π§΅
The last line is a hoot.
"However the potential inflammatory nature of these LNPs was NOT assessed."
Who has time for petty details when moving at the SPEED OF SCIENCEβ’οΈ? >
They injected saline (PBS) vs the LNPs in the skin and the muscle and found:
In both skin and muscle the LNPs quickly provoke an inflammatory reaction, below the skin on the right gets noticeably red. >
The far right is the inflamed muscle cell. >
They noticed an interesting effect >
Massive inflammation and increased weight in the muscle.
If the LNPs were to go off-target and circulate widely in the body, is there another muscle π which might be affected? >
Thousands of genes were upregulated. >
"...we show that LNPs, alone or complexed with control noncoding poly-cytosine mRNA, are highly inflammatory in π, likely through the engagement and activation of various distinct and convergent inflammatory pathways." >
Next, they inoculated the mice intranasally and found similar striking results. >
The LNPs made it look like the mice were chain smokers. >
The higher the amount of LNPs, the quicker the death. >
On the left is saline injected mouse lung. On the right is the LNP-injected mouse lung, an image which may be somewhat familiar to followers of Dr. Burkhardt. >
2 years ago Richard Hirschman bravely put his images on social media and it started me thinking about mechanisms which could cause such tough rubbery clots. >
Where they in the bodies of unvaxxed with C0VID,
or π or both?
Unclear.
What became clear is, that there are mechanisms for persistent clots in the bodies of both.
#MicroClots #TeamClots #TinyBubbles #LetItAllHangOut #DiamondsOnTheSoleOfHerShoes>
What happens when a lab created chimeric π¦ with gene inserts of HIV, is used as a template for a gene therapy, which also includes an HIV fragment as a stabilizing agent? >
Millions around the π are π from a pandemic panic
created by a chimeric SARS π¦ released from a
bi0weapons 𧫠conducting Gain of Function research
with πΊπΈ data & π° directed by Dr. Anthony Fauci. >
Fauci offshored risky GoF research to foreign labs like the Wuhan Institute of Virology in order to skirt U.S. regulations and continue research with pandemic pathogens. >
Research showing SARS2 proteins self assemble into amyloid aggregates and readily enter neurons to reduce their viability and mitochondrial respiration. > threadreaderapp.com/thread/1840761β¦
Scientists put the peptides in a soluble solution, which reduced their ability to form the more toxic fibrils and crystals, but still reduced the cells' ability for mitochondrial respiration. >
This finding indicates that repeat (even mild) COVID infections can cause amyloid build up, and have worrying implications for long term neurodegeneration, even if the "brain fog" is temporary after SARS2 infection.
Somewhat similar to repeat head trauma causing TBI. >
SARS2 can: persist, cause accelerated aging in every organ, cause activation and exhaustion of T cells
(via S and N proteins) in a feed forward loop mechanism, cause immune deficiency. >
#Lowdown #FlyingV #DontBringMeDown #Stay #KeepItComingLove #ILoveLucyJobSwitching