John R. Houk, Blog Editor
October 10, 2022
Naomi Wolf web capture 9/27/22
Dr.
Naomi Wolf (Ph.D. Literature) has a post to ponder on
FrontPageMag.com
Lipid Nanoparticles (LPN) in the mRNA Jab. The article is full of science that
might numb the mind devoid of science expertise (like me). ERGO, I
suggest you get to the complicated science, skip to the conclusion segments of
the article. The irony behind Wolf is she is typically a Liberal yet refuses to
comply with Left-Wing lying-manipulated science that twists facts to brainwash
people into mRNA compliance.
The Wolf article is entitled, “Lipid
Nanoparticles: Are They Subtly Changing Human Beings?” The Wolf
article is more about observing the probable Jabbed and wondering if the
documentation forced to reveal the content of the mRNA Jab and forced adverse
side-effects might be manifesting among the Jabbed populace (who have not
succumbed to a Jab death - yet). The article is lengthy but worth the read.
Come back and finish reading if necessary.
There is mention of a Glazov Gang interview with Wolf on
Rumble from 9/27/22 discussing the effect of the mRNA Jab on human sexuality
entitled, “No
Mojo in the Air: The Vax’s Killing of Sexual Desire”. I’m cross
posting the video after the FrontPageMag article.
JRH 10/10/22
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Lipid Nanoparticles: Are They Subtly Changing Human
Beings?
Are essential human qualities being destroyed by
PEG-coated industrial fats?
October 10, 2022
Visit Dr. Naomi Wolf’s Substack.com.
Some of my essays are grounded in politics, the economy, the
material world. Others reference the medical and scientific insights of the War
Room/DailyClout Pfizer Documents Research Volunteers, along with other
principled medical and scientific experts.
This one asks questions. Please read it in that spirit.
The spike protein haunts some of the good “dissident
doctors” and honest scientists. The mRNA fragments, for their part, profoundly
disturb others; and all for good reasons.
But it is the lipid nanoparticles (LNPs) in the mRNA
injections that keep me up nights, feeling that the dystopia on earth has now
fully arrived. And the reasons for that includes questions that border on the
metaphysical; as the LNPs, it seems to me, are able to negatively affect the
very essence of our humanity.
I recently had the bizarre experience of going to Manhattan
after a wave of “boosters” had been rolled out. I remember standing on a
crowded rooftop bar on top of a boutique hotel; attractive couples flirted at
tabletops; singles crowded the cocktail area; the sun shone, and everything looked
normal. But I kept having the disconcerting sense that I was standing inside a
hologram. I could not figure out what was wrong, until I realized — it looked like
a crowd, but it did not feel like a crowd. I could see the
people, of course, all around me, but I could not feel that
dense, joyful, passionate, sparky, fractious energy of a human crowd, pre-2020.
I checked on what it felt like while walking on the city
streets, and my impression was confirmed. There they were, the usual Manhattan
throngs, surging along the sidewalks — but they were like pictures, like
brightly dressed ghosts. The massive energy field —that sense of an island as a
pulsing human generator, the electricity that had galvanized generations of
newcomers to Manhattan — that was simply gone.
Not only was that overall energy gone. I noticed too that,
as Jamie
Glazov and I discussed recently on his podcast, the “mojo”, the
sexual energy, of Manhattan’s crowds, was gone as well.
The island used to be thronged with the rhythms of people
whose crossing of one another’s paths was like a flirtatious dance. There was a
beat to the city — the human beat of sexuality and creativity and joy.
Men and women — women and women, men and men — now barely
looked at one another. That dance of attraction, that flash of flirtation, that
sideways glance that the streets of Manhattan always yielded between passing
strangers and have done since the city began — the play of sexuality itself —
was so subdued or diluted as to be hard to sense or see at all.
I walked into restaurants and hotels, and the formerly
beautiful young women tasked with greeting visitors, looked like dancers in a scene
out of a 19th-century Dance Macabre. They were uniformly pale, or yellowish, or
had a grey cast to their complexions; they had circles under their eyes. The
glow of good circulation, the radiance of health and sexual energy, all of
which have been considered attractive for as long as humans have been courting
— was gone.
Crowds themselves were altered. Young adults were limping,
at scale. Men and women in their forties and fifties, who looked as if they had
been recently healthy, were now moving like eighty year olds. People in vast
numbers, of all ages, walked as if it was hurting them to move. Even teenagers
and older children moved like zombies or robots — drifting, with seemingly no
energy to spare. Smaller children did not squirm or race around. They sat
vacantly on park benches or in restaurants. Or they drifted like little wraiths
beside their parents, focused on nothing.
What happened? What happened to humanity?
Many have described their loved ones being altered in some
indefinable ways, after they have been injected with mRNA vaccinations.
People have spoken to me in distress about how they can’t
seem to feel the physical presence of their loved ones,
post-vaccination.
It looks like the same person, they say with grief, if a bit
paler, a bit more fatigued and ethereal.
But it doesn’t feel like the same person.
Their thinking may be more rigid, their loved ones report
sadly. They may be emotionally brutal. Attachments can seem less passionate.
Hugs more chilly.
Body workers and physical therapists have spoken about their
vaccinated patients’ temperature being now altered, their blood flow patterns
changed, even their “energy fields,” as they put it, being drained or weakened
(hey, I am from California).
This essay asks questions about what could
possibly cause inchoate changes in people post-mRNA vaccination and asks
whether the lipid nanoparticles themselves may be profoundly altering human
beings. Again, I am not proposing answers here, but simply exploring
possibilities.
We know the physical cost of lipid nanoparticles, due to
some recent pioneering research.
We know, for instance, that lipid
nanoparticles cause inflammation. Dr. Robert Chandler of the War
Room/DailyClout Pfizer Documents Research Volunteers re-established that, and
it is also a fact that has been known for years.
We know that the LNPs, which their manufacturers boast can
cross every membrane in the human body, cross the placenta, as fetal-maternal medicine
OB/GYN Dr. James Thorp has demonstrated. This is one reason the
lies to pregnant women of pharmaceutical, medical, and government spokesmodels,
in swearing that the mRNA injection ingredients could not cross the placenta,
are so egregious.
We know that the LNPs do cross
the blood-brain barrier — indeed, they were designed to
do that: some of their earliest medical uses involved the delivery of medicine
across the blood-brain barrier, to target brain tumors.
We know that Pfizer partnered this year with Acuitas
Therapeutics, a private company based in Vancouver, Canada, which manufactured
lipid nanoparticles, to bring ten more mRNA-LNP-based vaccines into the market:
‘“Our swift delivery of the world’s first mRNA-LNP-based
vaccine made clear the promise of mRNA-LNP technology,” said Mikael Dolsten,
M.D., Ph.D., Chief Scientific Officer and President, Worldwide Research,
Development and Medical of Pfizer Inc.
“We are making significant
investments to harness the power of the mRNA-LNP technology and deliver
potential new breakthrough vaccines and therapeutics that address significant
unmet needs for patients. This agreement expands our LNP capabilities and
allows us to explore more projects within our existing vaccines area and new
therapeutic areas where mRNA-LNP technology holds potential for success.”
“Acuitas is extremely proud that its LNP technology
contributes to the success of COMIRNATY® and is excited to be working with
Pfizer to advance new vaccines,” said
Acuitas Therapeutics’ CEO, Dr. Thomas Madden.
So:
Industrial fats treated with polyethylene glycol (PEG) can
cross every membrane in the human body. Including the brain.
What could possibly go wrong?
My own aversion to LNPs — an aversion that led me not to
choose to receive an mRNA injection — arose from simply reading on various LNP
production and distribution websites, how still-experimental, and how weirdly
off-the-shelf, this material is: you can order lipid nanoparticles, just as you
can order polyethylene glycol, from various supply companies who will “partner”
with manufacturers, few questions asked, in drug or experiment formulation.
“Creative Biolabs” is one such:
“Features of Our Services
·
One-stop and customizable LNPs preparation
·
The scalable proprietary manufacturing process
·
High-cost performance
Please contact
us for more information.”
I am an English major. I am not a medical doctor.
But even I can see possible serious problems in relation to
humanity being saturated, via every membrane, with lipid nanoparticles. Human
beings are more than our bodies. So this is a massive experiment on the very
essence of what makes us human.
Lipid nanoparticles are not medicines. They are a delivery
system.
They are composed of tiny objects, minute
particles of industrial fats, as noted above, that biodistribute into your
bloodstream and lodge, as Dr. Chandler showed, into various of your organs,
including your brain; and including, if you are a woman, accumulating in your
ovaries.
In the case of the mRNA
injections, the LNPs are coated with four lipids including PEG, a
petroleum byproduct. PEG is a thickening agent, that is in laxatives, and in
creams and cosmetics.
Structure
of Typical LPN Formulation Diagram
Many people have noticed that their loved ones in remission
from cancer, or whose cancers were long resolved and now in the past, have
suffered resurgences of raging cancers post-vaccination.
PEG, according to the David Suzuki Foundation, and other
critics of chemical additives, is a carcinogen:
“Depending on manufacturing processes, PEGs may be
contaminated with measurable amounts of ethylene oxide and
1,4-dioxane. i The International
Agency for Research on Cancer classifies ethylene oxide as a
known human carcinogen and 1,4-dioxane as a possible human carcinogen. Ethylene
oxide can also harm the nervous system ii and the California
Environmental Protection Agency has classified it as a developmental toxicant based
on evidence that it may interfere with human
development. iii 1,4-dioxane is also persistent. In other words, it
doesn’t easily degrade and can remain in the environment long after it is
rinsed down the shower drain. 1,4-dioxane can be removed from cosmetics during
the manufacturing process by vacuum stripping, but there is no easy way for
consumers to know whether products containing PEGs have undergone this
process. iv In a study of personal care products marketed as
‘natural’ or ‘organic’ (uncertified), U.S. researchers found
1,4-dioxane as a contaminant in 46 of 100 products analyzed.
While carcinogenic contaminants are the primary
concern, PEG compounds themselves show some evidence of
genotoxicity […] and if used on broken skin can cause irritation and
systemic toxicity. viii The industry panel that reviews the safety of
cosmetics ingredients concluded that some PEG compounds are not safe
for use on damaged skin (although the assessment generally approved of the use
of these chemicals in cosmetics). ix Also, PEG functions as
a “penetration enhancer,” increasing the permeability of the skin to allow
greater absorption of the product — including harmful ingredients.”
[https://davidsuzuki.org/]
So with an mRNA vaccine, you are getting lipid
nanoparticles, that are crossing every membrane in the human body — and that
are coated
with a potential carcinogen — traversing your bloodstream and
lodging in the organs in your body.
Can this hurt your heart?
A thoroughly ignored March 2022 study
from Metabolism Open Journal, “Potential
implications of lipid nanoparticles in the pathogenesis of myocarditis
associated with the use of mRNA vaccines against SARS-CoV-2”, made the very
reasonable case that myocarditis could be caused by the lipid nanoparticle
sheath on the mRNA vaccines. (COVID Spike Protein is also documented
to cause this kind of damage).
The 2021-22 Hong Kong study of mRNA injections in mice,
“Intravenous Injection of Coronavirus Disease 2019 (COVID-19) mRNA Vaccine Can
Induce Acute Myopericarditis in Mouse Model,” the one that I use as Exhibit A
in my argument that the mRNA injections are a CCP-overseen and manufactured
bioweapon, showed visible white patches on the hearts of mice
post-second vaccination. What is causing those white patches?
According to anecdotal reports from medical workers, the
hearts and lungs of severely vaccine-injured patients are also showing white
patches and even “crystallizations.” The blood
clotting problems faced by the vaccinated are now well established,
and blood clots and thrombocytopenia abound in the Pfizer documents. Many
reasonable hypotheses have been presented for the vascular and blood damage in
mRNA vaccinated people, but the industrial-fats nature of the LNPs haunt me:
could these harms be affected or even possibly be caused by something as basic
and mechanical as the unstable, clumping LNPs?
A casual
aside that disturbs me considerably, in many peer-reviewed studies of
nanoparticle medicine, is that many kinds of LNPs are solid at room and body
temperature.
Some LNPs that are solid at room temperature, are liquid
when chilled.
Is the instability of LNPs as dependent on temperature,
affecting human beings?
I do not know if any of this variation in solidity and
temperature is germane to the mRNA vaccines — there is so much we do not know;
but the fact that both the Moderna and Pfizer mRNA injections had, at the
rollout, to be kept super-chilled — between -20° and -70° Celsius, the latter
“colder than Antarctica” — has had various mushy, ever-changing explanations.
This November 2020 National Public Radio (NPR) article, for
instance, explains the need for ultra-cold temperatures as having to do both with
the mRNA and with the LNPs. It quotes Margaret Liu, of the International
Society for Vaccines:
‘“Here’s an analogy: Think of the vaccine as a chocolate bar
that melts easily. Just as there are ways to keep the chocolate from melting
into goo, there are things the drugmakers did to protect their COVID-19
vaccines.”’ The first step, Liu says, was to modify the mRNA nucleosides — the
“building blocks” of the RNA vaccine. ‘”They’ve used modified versions because
those are more stable,”‘ she says.
The next step was to use lipid nanoparticles, which, Dr Liu
explains, ‘”…is kind of like putting your chocolate inside a candy coating —
you have an M&M, so the chocolate doesn’t melt.”
But even with the stabilized building blocks and lipid
coating, the mRNA could still fall apart easily, which is why
the vaccine is frozen.”’
Dr. Margaret Liu is not some random physician, cited by NPR.
She is Chairman of the Board of the International Society for Vaccines.
As her
LinkedIn profile notes:
“Dr. Liu is known as ‘The Mother of DNA Vaccines’ a vaccine
technology that paved the way for authorized COVID mRNA vaccines and which is
licensed for veterinary applications and is considered crucial for addressing
diseases which emerge due to pathogens that cross between humans and animals
(One Health). She was instrumental in establishing the WHO Initiative for
Vaccine Research, was on the committee that wrote WHO regulatory guidelines for
DNA vaccines, and is the scientific lead for the WHO group drafting recommendations
for mRNA vaccines.”
Dr Liu is also funded by the Bill and Melinda Gates
Foundation. Indeed, she is the Senior Advisor to the Bill and Melinda Gates
Foundation on the billion dollars
that the Foundation invested in — vaccines.
And…Dr. Liu is herself a holder of multiple vaccine
patents:
“After leading vaccine and gene
therapy research at two companies and filing various patents, Margaret was
asked to be the senior advisor in vaccinology for the Bill & Melinda Gates
Foundation. This, as well as helping establish the World Health Organization’s
Initiative for Vaccine Research, enabled her to expand from developing
technologies for global vaccines to the broader arena of global health.”
So — Dr.
Liu is advising the WHO, that is funded by China, and also by Bill
Gates: “The Gates Foundation is the second-largest contributor to the WHO. As
of September 2021, it had invested investing nearly $780 million in its
programs this year.”
Dr. Liu advises the WHO on mRNA vaccines, which are
manufactured in a Memorandum of Understanding (MOU) with China — per my
Substack “Facing the Beast” — and which are using intellectual property (IP)
now transferred, per BioNTech’s SEC filing, to China.
Thus, Dr. Liu, funded by Bill Gates, and advising Bill Gates
on his billion-dollar investment in vaccines; is also advocating to NPR,
a US government news agency, for the use of mRNA vaccines, which are paid for
by the US government, a payment that then profits China and — Bill Gates.
Let’s follow Dr Liu’s logic: the mRNA vaccines, in order to
act “kind of like putting your chocolate inside a candy coating — you have an
M&M, so the chocolate doesn’t melt” in Dr Liu’s eloquent words — (these are
your tax dollars at work) — must be super-chilled.
But what happens to these materials when they are — in the
human body? What happens to the materials when… the materials are no longer
super-chilled?
This study, “Achieving long-term stability of lipid
nanoparticles: examining the effect of pH, temperature, and lyophilization,” by
Ball, Bajaj and Whitehead, published in the International Journal of
Nanomedicine in 2017, checked the stability and behavior of LNPs
during various freeze-thaw cycles, and found that temperature alterations
indeed degraded the efficacy of LNPs.
The study also found clumping or changes in LNP
particle size, depending on temperature:
“Storing the LNPs at −20°C resulted in an increase in
z-average particle size as well as a significant amount of aggregation.
[Italics mine. This is the temperature at which Moderna is supposed to be
stored]. During the freezing process, a phase separation occurs that results in
the formation of an ice phase and the nanoparticle-concentrated solution phase.
The separation of phases has been shown to lead to irreversible fusion
of nanoparticles and subsequent aggregation. [Italics mine.]
Additionally, ice crystal formation during freezing could have exerted
mechanical stress on the LNPs, causing them to increase in size. The damage
done to the LNPs, post freeze–thaw, was lessened with the addition of the
cryoprotectants, trehalose, and sucrose, in a concentration-dependent manner.”
[Rebecca
L Ball,1 Palak Bajaj,1,2
and Kathryn
A Whitehead1Int J
Nanomedicine. 2017; 12: 305–315. “Achieving long-term
stability of lipid nanoparticles: examining the effect of pH, temperature, and
lyophilization,” Published online 2016 Dec 30. doi: 10.2147/IJN.S123062 PMCID:
PMC5221800 PMID: 28115848]
So again — I am not a medical doctor or a scientist, and
maybe this unstable and highly problematic behavior of LNPs when temperatures
vary — and the fact that they clump and alter in irreversible ways at
super-cold and then warmer temperatures — is not relevant at all to our current
predicament; and maybe the fact that LNPs alter at various temperatures, does
not in any way help to explain the way vaccinated people are collapsing, having
strokes and heart attacks, suffering blood and lung clots, and sustaining
horrific menstrual damage.
But… maybe this feature of lipid nanoparticles is worth a
look.
Moderna is supposed to be stored at -20° Celsius, as you
recall.
But these are the 2022 CDC
storage and handling guidelines for Moderna:
“Delivery Vaccine will arrive frozen from the
manufacturer between -50°C and -15°C (-58°F and 5°F). [Italics mine].
Unpack, following the manufacturer’s guidance, immediately.
The vaccine may be stored in a freezer or refrigerator. Guidance follows.
Storing UNPUNCTURED Vials
Freezer Vaccine may be stored between -50°C and -15°C (-58°F
and 5°F) until the expiration date ƒ
Store vials upright in the tray or box protected from light ƒ
Do not store with dry ice or below -50°C (-58°F) ƒ
Determine the expiration date by scanning the QR code on the
outer carton or go to modernacovid19global.com/vial-lookup [This
alone should cause alarm. There is no expiration date on the vials! You have to
scan a digital code or go online to check the sell-by date!].
Refrigerator Vaccine may be stored between 2°C and
8°C (36°F and 46°F) for up to 30 days. ƒ[Italics mine].
Do NOT refreeze thawed vaccine ƒ
Store vials upright in the tray or box protected from light ƒ
Use tracking labels to monitor the 30-day beyond-use date
Cool/Room Temperature
Vaccine may be stored between 8°C to 25°C (46°F to 77°F)
for a total of 24 hours. [Italics mine.]
Do NOT refreeze thawed vaccine ƒ
Store vials upright in the tray or box protected from light ƒ
Track this 24-hour beyond use time
Storing PUNCTURED vials
Vaccine may be stored between 2°C and 25°C (36°F and 77°)
for up to 12 hours ƒ[Italics
mine]
Discard vial and any remaining vaccine after 12 hours ƒ
Thawed vials can be handled in room light conditions ƒ
Total storage at 8°C to 25°C (46°F to 77°F) must not exceed
24 hours”
So — either the vaccine never needed to be stored at -50° to
-20° Celsius; “colder than Antarctica.” Or — it did, and the CDC is
contradicting the manufacturers’ warnings, and telling clinics, what the heck,
none of that matters, you can refrigerate it to up to 46°
Fahrenheit — a cool Fall day — for 30 days, or hey, you can keep it at room
temperature for 24 hours, indeed, at temperatures up to 77° Fahrenheit — a
Spring day in Florida. Whatevs.
But unless something fundamental has changed since 2017, or
unless the vaccines’ handling needs have changed since rollout, this
variability in storage guidelines may well risk affecting the behavior of the
LNPs.
Another commentator declared that, “The Pfizer COVID-19
vaccine must be stored at ultra-low freezing temperatures, about -100 degrees
Fahrenheit. This temperature falls well below what’s found in a standard
freezer,” explains
Dr. John Cooke, medical director of the RNA Therapeutics Program at
Houston Methodist. “In fact, the type of freezers needed to store this vaccine
long-term aren’t ones you’ll find in a doctor’s office, drug store or even most
hospitals. The Moderna COVID-19 vaccine also needs to be kept frozen for
long-term stability, but it can be kept in a standard refrigerator in a clinic
for a few weeks.”
So — what then? Does the material need to be
ultra-super-cold frozen to work at all? Or totally — not? Just pop it in the
fridge, dude?
The gibberish
continues: This CDC temperature log from August 2021 says that
above -76 degrees, Pfizer storage temperature is out of range.
But this one, from September 2022, says up to 46° Fahrenheit
– in the fridge – for 30 days, is
just fine.
This one will baffle you even more. It also says that the
vaccine must be stored at as low as -130° to -76° Fahrenheit, but it can — also
be kept in the fridge at up to 46 degrees Fahrenheit.
And — you can expect that COVID will not go away, since the
vials depicted march
their way through all of 2023, January to December.
And what do you make of this Alice-in-Wonderland-style
instruction?
“Use tracking labels to monitor the 10 weeks beyond-use
date.”
So — are these wildly varying temperature requirements
science-based requirements?
Or are they fungible?
Are these impossible instructions meant to keep us all
protected?
Or possibly even to ensure that — mistakes will be made?
Karen Kingston, the whistleblower regarding pharmaceutical
production problems, recently added to the mass of evidence we have located
here, confirming that the vaccines, like the virus, originated under the aegis
of the CCP. Kingston noted that per CDC, nine of the CDC
trials for the 2020 vaccine rollout, were overseen by China. One,
I must note, unbelievably, was overseen by the People’s
Liberation Army.
Kingston also reported that the lipid nanoparticles are
manufactured in China.
I checked, and she is right.
A Chinese company that makes lipid nanoparticles, WuXi, did not stop at making
LNPs for Pfizer; rather, it recently bought the Pfizer production plant
in China for an undisclosed sum, bought up other European drug manufacturing
plants, and opened a production plant in Worcester, Massachusetts.
So: I had shown earlier that Pfizer had a Memorandum of
Understanding (MOU) with a Chinese pharmaceutical company, Fosun Pharmaceuticals. But
now we see that a Chinese company, WuXi, has bought part of Pfizer.
This happened in the first half of 2021 — when the most
damaging part of the mRNA vaccine rollout was at its height.
The WuXi Worcester, MA, facility is the third CCP-owned plant we have confirmed that is
manufacturing US mRNA injections, including the lipid
nanoparticles, that will go or are going into American bodies, in America, this
year, 2022.
WuXi Buys Pfizer China Plant
18.03.2021 – China’s WuXI
Biologics has agreed to buy Pfizer’s biologics manufacturing facilities in
Hangzhou for an undisclosed price. The transaction is expected to close in the
first half of 2021. The Shanghai-based company said the acquisition will
immediately boost its capacities for commercial drug substance (DS) and drug
product (DP) capacities to address surging manufacturing demand.
The GMP facilities include two 2,000 liter single-use
bioreactors expandable to four 2,000 liter bioreactors, as well as capacities
for vial filling and pre-filled syringes. Chris Chen, CEO of WuXi Biologics said DS
and DP capacities are in urgent need now globally.
The company added that with total estimated capacity for
biopharmaceutical production planned in China, Ireland, Germany, the US and
Singapore exceeding 300,000 liters after 2023, it will provide its
biomanufacturing partners with a robust and premier-quality global supply chain
network.
The agreement with Pfizer follows purchases earlier this
year of plants in Switzerland and Germany. The biologics group is also building
a biomanufacturing campus in Worcester, Massachusetts, USA, which is scheduled
to go into operation in 2022.”
Given how temperatures grossly affect the behavior of lipid
nanoparticles — is all this casual variability in temperature and storage
instructions — safe? Is the manufacturing of an unstable
injection which is now largely or entirely in the hands of our existential
enemies — safe?
This scenario, and the questions it raises, and the fact
that this injection is manufactured by our existential adversary as my essay
“Facing the Beast” had proven, remind me of those crime scene riddles in which
the murder weapon is an icicle that has melted and so is now not visible, or
that is in some other way perfectly vanished or obscured.
A medium that carries the mRNA and spike
protein — the active ingredients which are naturally enough demanding the attention
of most — but a medium that itself could cause problems to the
blood, brain, ovaries or other organs, depending on temperature — would be a
hell of a way to kill or disable a targeted population slowly, mystifyingly,
and with no fingerprints.
****
Then there is the way that the lipid nanoparticles may be
affecting humans in other ways. Many have spoken, as I noted above, about how
their loved ones, especially right after injections, can seem intellectually
rigid, or emotionally cold, or altered in their thinking.
Can these lipid nanoparticles possibly help to explain this
devastating, hard-to-describe change in many of those around us?
We know that LNPs are gumming up, in both men and women, the
factories of hormones; Dr. Chandler has shown that they disrupt the ovaries,
and Amy Kelly has shown that they disrupt the Leydig and Sertoli cells, the
factories of masculinity, the generators of testosterone in the testes.
Thus the LNPs are indeed impairing sexual signaling and even
changing, and dampening or deleting, human desire.
The lipid nanoparticles may hold a clue to these subtle
changes. The LNPs may indeed be changing those we love by possibly affecting
nerve conductivity.
I am sensitive to neurological issues since I have a serious
neurological condition myself; and I am, as a result, fascinated by the
so-fragile and so-magical nature of nerve conductivity — how temperament and
sensation and mobility and even thought itself can depend on the health or
interruption of neural impulses.
I kept thinking about how the brain and the heart depend on
neural impulses; and I wondered if there was a clue there for this sense of
“absence” that many report, in interacting with their loved ones
post-vaccination.
I asked Dr. Chris Flowers, one of the WarRoom/DailyClout
Pfizer Documents Research Volunteers, if the LNPs could affect the nerve
conductivity of the brain or of the heart.
He responded with a document, “Conjectural Analysis of LNPs
Affecting Nerves in Brain and Heart,” that starts with the effect of LNPs on
the brain:
“The nervous system is the mechanism that the brain uses to
communicate with various organs in the body.
It is composed of neurons, composed of axons surrounded by
myelin supported by oligodendrocytes. The axons are wrapped in myelin, which acts
as an electrical insulator.
Axons are the nerve structures themselves.
Oligodendrocytes form the electrical insulation around the
axons of nerve cells in the central nervous system (brain).
These cells grow the myelin on up to 5 nearby axons through
their feet (dendrites).
These are important cells, as they also participate in the
maintenance of the nerve, providing sustenance to the neurons and maintaining
the long-term stability of myelin.
In the peripheral nervous system, a similar cell to
oligodendrocytes, with the same function, are the Schwann
cells.
For nerves to act as rapid conductors of messages, it
requires that the axons (nerves) are coated with sheets of myelin.
So: what could happen if these supporting cells malfunction?
1. Oligodendrocytes – as these are in the brain,
could malfunction due to either LNPs or to Spike Protein; either could cause
them to lose the myelin sheath. This
damage to the myelin sheath could cause mental issues or neurological symptoms
or signs. [Italics mine.]
2. Schwann cells; similar to damage within the brain in
oligodendrocytes, these cells, if damaged, would allow the myelin surrounding
the nerves to deteriorate, then effectively to be removed. This deterioration
could end up causing symptoms such as multiple sclerosis (MS), and this
degradation could also be responsible for some of the many known neurological
adverse events (AEs) demonstrated in the Pfizer documents.
There is a possibility of LNPs being absorbed into the
myelin sheaths themselves, or even into the Oligodendrocytes. In either of
these cases, the cells would begin to malfunction, and the end result is a
degree of demyelination or even complete demyelination. It has been conjectured
that deterioration in the function of Oligodendrocytes could be a cause of ‘aging’/brain fog/dementia.
[Metabolism
and function of lipids in myelin]
Another potential cause of brain damage would be the spike
protein being introduced into the brain due to the LNP’s ability to cross the
blood-brain barrier.”
So the answer is: yes, lipid nanoparticles could conceivably
affect the nervous system and thus, specifically, the brain.
The fact that lipid nanoparticles could indeed be degrading
human nervous systems, meaning degrading the human spirit itself, is abundantly
clear in Project Director Amy Kelly’s search in the Pfizer documents, using our
search tool Abstractor, of variations on the word “myelin” and
“myelitis”. On this myelin, on these impulses, depend thought, movement,
dreams, imagination, prayer, desire and fulfillment, the sense of touch and
sensation. I remember having been stunned to see mentions of MS as a side
effect in the Pfizer documents – how could that be? And Ms Kelly’s results are
even more stunning, even as Dr Flowers’ explanation makes clear exactly
how these
horrifying results could have come to pass:
“p. 21, Table 7, section “Neurological AESIs
(including demyelination) Search criteria: Convulsions
(SMQ) (Broad and Narrow) OR Demyelination (SMQ) (Broad and
Narrow) OR PTs Ataxia; Cataplexy; Encephalopathy; Fibromyalgia; Intracranial
pressure increased; Meningitis; Meningitis aseptic; Narcolepsy“: “Most
frequently reported relevant PTs (˃2
occurrences) included: Seizure (204), Epilepsy (83), Generalised tonic-clonic
seizure (33), Guillain-Barre syndrome (24), Fibromyalgia and Trigeminal
neuralgia (17 each), Febrile convulsion, (15), Status epilepticus (12), Aura and
Myelitis transverse (11 each), Multiple sclerosis relapse and Optic
neuritis (10 each), Petit mal epilepsy and Tonic convulsion (9 each),
Ataxia (8), Encephalopathy and Tonic clonic movements (7 each), Foaming at
mouth (5), Multiple sclerosis, Narcolepsy and Partial seizures (4 each),
Bad sensation, Demyelination, Meningitis, Postictal state, Seizure
like phenomena and Tongue biting (3 each);”
p. 30 – encephalomyelitis, Acute flaccid
myelitis, Anti-myelin-associated glycoprotein antibodies positive;
Anti-myelin-associated glycoprotein associated polyneuropathy
p. 31 – Autoimmune demyelinating disease, Axonal
and demyelinating polyneuropathy,
p. 32 – demyelination, Chronic inflammatory
demyelinating polyradiculoneuropathy, Chronic recurrent multifocal
osteomyelitis, Demyelinating polyneuropathy, Encephalomyelitis
p. 33 – Herpes simplex meningomyelitis, Herpes
zoster meningomyelitis
p. 34 – Leukoencephalomyelitis
p. 35 – Marburg’s variant multiple
sclerosis, Multiple sclerosis; Multiple sclerosis relapse; Multiple sclerosis
relapse prophylaxis, Meningomyelitis herpes, Myelitis; Myelitis
transverse, Neuromyelitis optica pseudo relapse, Neuromyelitis optica
spectrum disorder, Noninfectious myelitis, Noninfective
encephalomyelitis
p. 36 – Osmotic demyelination syndrome, Primary progressive
multiple sclerosis, Progressive multiple sclerosis; Progressive relapsing
multiple sclerosis
p. 37 — Relapsing multiple sclerosis;
Relapsing-remitting multiple sclerosis, Secondary progressive multiple
sclerosis, demyelinating polyneuropathy
p. 38 – Tumefactive multiple sclerosis”
So these industrial fats, saturating as they do through
every membrane, are crossing the blood-brain barrier. Thus they can indeed be
changing the very brains of our loved ones.
The lipid nanoparticles cross every membrane. Brain. Heart.
Testes. Ovaries.
Thoughts. Love. Desire. Conception. Dreams. Imagination.
Inspiration. Perhaps even the sense of God.
So meanwhile, until we know more — consider:
Could these results — damaged hearts, lowered sexual desire
and potency, lessened human bonding, the various forms of male and female
sterilization on which we have reported earlier, the rigidified thinking due to
industrial fats accumulating in the brain, not to mentioned the physical
dangers of industrial fats and carcinogens zooming through the bloodstreams of
the citizens of the West — with each booster adding to the body’s burden of
lipid nanoparticles — all be — possibly — features of this
bioweapon?
What better way to kill the hard-to-oppress characteristics
of free men and women: degrade their energy, their aspiration, their skills at
forming bonds – indeed, their very ability to engage in nuanced, expansive,
compassionate critical thought?
What better way, indeed, to murder the troublesome West?
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Rumble VIDEO: No
Mojo in the Air: The Vax’s Killing of Sexual Desire
Posted by The
Glazov Gang
Published September 27, 2022
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