INVENTING RECEPTORS LIKE ACE2: DEMOLISHING ANOTHER PIECE OF THE COVID NARRATIVE
Dr Scoglio’s questioning of the ACE2 enzyme as a receptor for the ‘SARS COV2/spike protein’ (@26min) ought to pique the interest of all functional genomic analysts. Enzymes attack, lyse and degrade substrates. Enzymes are catalysts. They are active. They are not attacked or invaded or conquered by substrates.
The ACE2 (angiotensin converting enzyme) is part of an inflammatory pathway called RAAS (renin-angiotensin-aldosterone) and central to the prescription of blood meds, specifically ACE inhibitors. Early in the plandemic, Dr Dietrich Klinghardt noted that ACE inhibitors exacerbated ‘viral,infection’ and ARBS (receptor blockers) protected, per the narrative. It makes more sense that nothing at all happens with ACE2, but for the inflammatory creation of many exosomes (possibly increased by the blood drugs) and declared to be ‘viruses’ (see earlier posts about the trif***ta blood drugs.)

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mRNA-ACE2 FOR “COVID” TREATMENT
Prescription blood pressure drugs cause respiratory illness by generating lots of inflammatory angiotensin, identified by lots of ACE2 exosomes, that is, ‘viruses’ (see @DrStefanScoglio and ACE2)
There are many ways to identify root cause/s of hypertension. We know the biochemical, enzymatic inflammatory pathway of blood pressure, and ways to correct it ... naturally.
And yet, look at the direction things are going in “medical science” with COVID virus/exosomes (not a surprise).

“Both ACE inhibitors and ARBs substantially increase ACE-2 activity in cardiac myocytes over one to two weeks. ACE-2 is also found on epithelial cells in the respiratory and gastrointestinal tracts.“ ~ Drugs and the renin-angiotensin system in covid-19

The systemic renin-angiotensin system in COVID-19

The RAAS Axis and SARS-CoV-2: From Oral to Systemic Manifestations

Rapid Generation of Circulating and Mucosal Decoy Human ACE2 using mRNA Nanotherapeutics for the Potential Treatment of SARS-CoV-2

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Dr. Tom Cowan presented at the Weston A. Price Foundation's annual Wise Traditions conference back in 2022. The presentation was recently uploaded to the Weston A. Price Foundation's Bitchute channel.

Part 1 of 2 - https://www.bitchute.com/video/Rj2igX7AJisW/

Part 2 of 2 - https://www.bitchute.com/video/8SKUtU7wEUEP/

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IF YOU WANT TO KNOW WHAT ACTUALLY MAKES YOU SICK, it helps to know what you/we are made of ...

Here, a partial list of things we are told are part of our makeup, for which there is no proof of existence or function, including DNA which varies among tissues and fluids, and many cellular organelles such as the ribosome (as in RIB) where the mRNA technology is said to replicate a ‘virus.’

Lipo layer (or unit) of the cell membrane
Ribosomes
Blood/brain barrier
Endoplasmic reticulum
Golgi apparatus
Receptors (eg, ACE2, opioid) in cell membrane
Synapses in nerves
Neurotransmitters
Lysosomes
Nuclear pores
An “immune system”
Autoimmunity
DNA is the mechanism of heredity
DNA is identical in all parts of the body
DNA codes one gene for one protein, and evolves uni-directionally from DNA to RNA to protein
Cristae in the mitochondria

Screenshot, Dr Tom Cowan presentation, Weston A Price, 2022, part 2
DNA addressed @45min

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“LONG HAUL COVID” or “LONG COVID”
If you want to start a pandemic, cobble together a bunch of symptoms, and give it a new name.
If you want to end a pandemic, break up the symptoms and give these new groupings of symptoms new names. (to paraphrase Dr Tom Cowan)

There is no disease, by definition, called “COVID” caused by a ‘virus’ called SARS COV2. These symptoms are the result of toxicity, mal-nourishment and trauma which are unique to each person ... and warrant a new name. There is an illness, but it is not “COVID.”

See previous posts on exosomes generated by blood drugs like ACE inhibitors, and Dr Stefan Scoglio.

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“TRANSFECTION” & “SHEDDING” of lipid nanoparticles in the mRNA injections
Reading these kinds of papers is like picking my way barefoot through a pasture dotted with fresh cow pies. For every citation claiming the existence of a “spike protein,” for instance, there is perpetual awareness of faulty methodology and assumptions (the PCR, antibodies and other surrogate markers). Others have identified the lipid nanoparticle or graphene oxide in the jabs to be the cause of damage, while the mRNA ‘spike’ and ACE2 have lost ground which makes sense since neither the glycoprotein nor the receptor, as described in the “COVID” narrative, exist. Further, there is the conflating of terms: exosomes, extracellular vesicles and nanoparticles; the language and the words require vigilance, else we find our toes squishing into newly laid hot moist cow dung.

“Lipid nanoparticles (or their natural equivalent, exosomes or extracellular vesicles (EVs)) have been shown to be able to be excreted through body fluids (sweat, sputum, breast milk) and to pass the transplacental barrier. These EVs are also able to penetrate by inhalation and through the skin (healthy or injured) as well as orally through breast milk (and why not during sexual intercourse through semen, as this has not been studied). It is urgent to enforce the legislation on gene therapy that applies to mRNA vaccines and to carry out studies on this subject while the generalization of mRNA vaccines is being considered.”

Current state of knowledge on the excretion of mRNA and spike produced by anti-COVID-19 mRNA vaccines; possibility of contamination of the entourage of those vaccinated by these products

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EXPOSURE & EXCRETION OF LIPID NANOPARTICLES
“Exposure of the human body to nanoparticles can occur accidentally through inhalation, skin contact, or ingestion.
In the case of inhalation, the possible routes of transfer of nanoparticles are the bloodstream (systemic), the lymphatic vessels, the gastrointestinal tract and the central and/or peripheral nervous system.
Excretion of PEG-coated LNPs is primarily through feces and urine and primarily through feces when they are > 80 nm in diameter.
LNPs can be excreted through saliva, sweat, and breast milk.
LNPs of size < 5 nm are rapidly excreted by the kidney.
Nanoparticles that are between 5 and 200 nm tend to have extensive blood circulation.
Larger LNPs have prolonged blood circulation and little renal excretion. Because of the size of LNPs, inhalation is the most direct route of entry into the pulmonary system.
Exposure can be intentional, as in the case of targeting or therapeutic nanoparticles, or unintentional, through inhalation or dermal exposure, due to the increasing number of industrial applications of nanoparticles.”

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"They lie to us, we know they're lying, they know we know they're lying, but they keep lying to us, and we keep pretending to believe them."
- Alexander Solzhenitsyn

They're Doing It Again! - Dr Sam Bailey
https://drsambailey.substack.com/p/theyre-doing-it-again

SIFTING THROUGH THE RUBBISH BIN
Stew Peters is a sensationalist, clearly. I say take what is useful, if anything, such as the bits about the use of thermography to identify inflammation and dismiss the rest.
In Washington, DC in the 90s, I worked in sustainability, environment and population growth, specifically, and then in energy, writing about cleantech (wind, solar, fuel cells etc) and managing demand-side reduction programs. All too many statements are made in the “truth-y-ish” movement on these two topics alone that are loaded with straight-up Stew Peters’ style hyperbole. I let them go.

https://jackanapes.substack.com/p/died-suddenly-is-typical-trash-from

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HARVARD LAW & CRITICAL THINKING?
My father was Harvard Law ‘59, Yale ‘56 (engineering), and Phillips Exeter ‘52. It was rumored that he belonged to Skull and Bones.
We are coming up on the first anniversary of his death; his obituary is posted on this channel. He was a lone man left standing, all his brothers and college friends pre-deceased him. My father did not die a year ago, in my mind. His slow demise began when his Yale Medical doctors in New Haven, whom he trusted implicitly, put him on “high blood pressure” and statin drugs. His last stand was walking into a rehab facility in Connecticut, de-mobilized to a wheelchair, and dying two years later, having never left.
He only harped about the drug regimen when the Yale doctors told him that he was pre-diabetic, a “side effect” of the other drugs. Several years ago, I asked him, implored, that he read the literature on those blood drugs ... to stop taking them. “I hear what you are saying but then the doctors talk at me and I can’t understand what they are saying, so I am taking them.” I asked that his wife read the literature. (“You know she can’t do that!”).
I said my goodbyes to him, in my heart, long before he stopped breathing, because I knew there was no turning back, no room for reasoning or thinking critically. The drugs effected his mind. COVID was in full swing, and his wife, as expected, bought the whole story, including the injections. He was going to stay locked up, to die there.

It has been said many times over the past two plus years that the more degrees someone has, the more difficult it is to reach them, to get them to think critically about their schooling and beliefs. About government and corporations and medicine. About their friends making money by lying to them and harming them and those they love.

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BEN SHAPIRO, HARVARD LAW, MEA CULPA
How long will it take the brainiac, Ben Shapiro, to grasp the fallacies of “germ theory” and the entire fraud that underpins the “vaccine” agendas?
https://thecovidblog.com/2022/11/04/tgif-misinformation-takedown-portal-between-facebook-biden-administration-exposed-ben-shapiro-vaccine-mea-culpa-and-25-plus-more-sudden-deaths/

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MODAFINIL & BLOOD PRESSURE
Yet one more drug ... pharmaceutical mysticism and sorcery.
https://nootropicology.com/does-modafinil-raise-blood-pressure/

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