Hi everybody. Uh I'm Dr. Randy Bach and we're here today with a very special episode of our coronairus conversations which we've been carrying on for far too
long. Um but you know they've been banging us over the head with Coronairus and so we have to fight back a little bit. Um I have what one of the the
upsides of the the great pandemic has been to meet great new friends and I count among them uh the brilliant uh
yeah that's that's right before his name the brilliant Mark Geraldo. He's in Paris and uh he comes up with one um uh
I was ecla would be the French word but he has uh you know brilliant thunderstrokes of of insight and clarity
and it's it's all the more so perhaps um uh because he's I don't think strictly speaking medically trained although he has had as a consultant some
associations with pharmaceutical companies and so forth. He'll explain that perhaps a little on his own. Um but uh he has come up with recently uh
through and I read his Substack and you can find it just copy down his name and put in Substack. Um he has great work um
on his Substack and most recently uh came across um the bolus theory which is in his words unified theory of some of
the um problems with the uh the V-word we can barely even say these days. Um, and um, not that V-word, but this
V-Word. And without further ado, I'm going to uh, turn the stage over to Mark. Um, and he can describe a little bit about what uh, he's he's getting at.
So, I apologize for the imperfect introduction. Maybe you can fill that fill us in a little bit.
Hi everyone. Um, so my name is Mark Gerardo. I know it's very hard to to say in English. Um
yeah, my background is in uh I'm a father of four. Um I live in Paris. Um I've traveled the world. Uh my
background is business. I have two MBAs actually. Uh worked for high-tech industry. Worked for Cisco for 15 years.
Um I'm mostly an expert in complex systems. I was an expert in automotive.
Um and I've worked also in biotech and pharma. Uh notably um I did a deep dive
four years ago into uh iminooncology uh working for an amazing French startup
that had developed a a universal therapeutic anti-cancer vaccine.
Um and um and it's my second time with you uh Randall. Uh yeah, back back by popular acclaim.
[laughter]
Um so the first time I I I I really had dug into uh the epidemiology uh of COVID
and found some uh very interesting stuff. Um and then um for the past uh
year and a half um I have been working on the on the Vword. Can we say it or not? I mean am I going to have to
it's going to be probably in the title so let's it's going to be complicated to not say it. So no the vaccine but but fundamentally
what I'm going to talk about is not specific to those vaccines. It's also true um for for other vaccines. Um and
uh the you know the whole thing started at Panda where where we met. Um when about
uh as soon as the um the vaccination campaign started I started to see things
in the uh epidemiology numbers that didn't didn't make any sense. Um uh and and and very frankly I'm it's pretty you
know it's pretty clear mathematically that what was happening was impossible.
It was simply the fact that you know the epidemic was starting back um in in as the fall was coming in September,
October and November peaked in November and started going down um in most most the western um or northern hemisphere. Mhm.
Um and then um the vaccination campaign started in most countries, you know, New Year's Eve basically or or the next day,
first of Jan 2021. And as soon as that happened, there was a complete inversion of of of
the curves. They they start going back up. And that that uh that kickstarted
that was a huge red flag for me because that's impossible mathematically because the reason the curves were going down
especially in the middle of of winter meant that that the susceptibles the people who were not
immune um were were depleted and you can't you can't refill uh deflated
stocks overnight. it it takes it takes at least a year for people to move, for people to age, for new uh new kids to be
born. Uh and that to me was a signal and and as I said in my latest uh COVID misbuster article
um and you were there, we we had um I was one of the rare at Panda that said something's going wrong with Roger
Hutchinson from um and and and Mike Eden um and nobody did wanted to believe us.
Um, and so I've I've been digging into what what what really is happening for
for a very long time. Um, and one of the highlight moments and you know I'm very hands-on. I look at details and I read
uh read ves and read a lot of things and one of uh good surprise I had was my
son my I have one of my son um vaccinated and started telling me he was he was he he wasn't feeling well and I I
truly you know speaking I panicked I was really um scared that he would have uh the things I was seeing elsewhere and I
had him checked Um he had d-dimers done etc. And he was fine. He was actually fine. He was he was overworked uh like
his dad. Uh but it was fine. And so it that to me was very important. It was it's it was
very important that you know the a lot of people are saying you know there's a camp that says um uh it's safe and
effective. There's there's a camp saying uh it's unsafe. Um, it's poison. Um, I'm
in the middle. Okay. It's um it's it's not safe, but it's not poison.
Right. Poison is something you give to every single person in the world and they have the same symptoms. They have the same problems.
I'm going to interrupt for one second. I warned you I might interrupt, but I I think there's actually a third category um which is pointless. Um you know,
[clears throat] I mean I I I I probably overlaps with yours. Um, but you know the the there is a vaccine for I think yellow fever and I don't know if it's a
good vaccine or bad vaccine but I just don't go near it because I have no need for it and I think for a lot of people the covid vaccines um should have been
like the yellow fever people who are not going to get sick or don't have any problems with children. So we've discussed this separately but I'm just going to put that out there as a thought bubble we maybe come back to.
Yeah I mean I I'm I'm not going to talk about effectiveness of the vaccines.
I've I've this one I'm is very clear to me. I've written about it in Substack.
There's there's there's I think the point you're making is a very good point, but we don't have time to to Fair enough. So, so just to frame this
for our our listener viewers, um we are really talking now about the modality, the mechanism from which side effects may uh be occurring. True.
Okay. Yeah. Actually, I'm I'm I'm going to say with a lot of confidence is is I it because every single step of the way
of my theory, I guess theories are proven. Um, every step of the way is is is factual. Okay. Material is factual,
etc. Um after that it's it it's hard for people to to to integrate
um because it's um it's a combination of things as often when you have disasters. You know if you
do root cause analysis it's rarely one thing. If it were poison people would have noticed it. It's the fact that you
have uh three different uh factors. Um so I should I join jump in?
Yeah. Well, let let's let's cut to the chase. You want me to put up your your your post or No.
Yeah, sure. I mean, you could put up the the post. I the the fundamentals of what I've dis discovered.
Um and I'm not the only one. I mean, people have been talking about that for some time. It's the fact that um in some
instances because um injection practices have have been changed in the past um 10
or 20 years. Um uh the injectors are nurses, doctors um and and professionals
are no longer aspirating. So many people uh h have been talking about that. The
question is okay so what you know so so they've changed that and when you asked
doctors um about it I I um I would go yeah go down. I mean that's okay. Uh
well that's a bit complicated to see but yeah that's it's it's okay. I mean maybe you can enlarge this and we'll start from there.
So um so the the first thing that you know I'm going to try and go through
chronologically we we um after Panda I started working with Steve Kirch and his and the team and there's there's a
number of people Robert Malone Peter McCulla was there Berham Bridto is there um and I was one of the the the lucky
few to be uh with with that team with Jessica Rose etc. and and Berum did um a
huge um um presence to to to the world by by asking early on to the Japanese
authorities the the distribution data in the mouse
and over in May 2021 we knew first of all that the vaccines were were not the particles were not staying in the
muscles and they were slowly but surely quite rapidly actually going to the bloodstream and then transfecting inside
the vascular system. Now that that really got me thinking um because the
mode of action of of the of the vaccines and you know all actually all of them
are transfecting vaccines. They are vaccines that bring um a foreign material, genetic material inside um
inside a cell to either produce an antigen or or to bring an antigen. Um now our our immune systems every day
destroy cells that are contaminated that way. Okay, there's it's systemic. It's it's systematic. Sorry. Mhm.
Every single cell that will be penetrated by a highly immunogenic
i.e. a a material that will have a a very strong will trigger a very strong
reaction uh to the um uh of the immune system will get destroyed. Right? That's the whole purpose of the vaccine. Right?
Uh now the the the the idea that everybody's forgetting that
it's the elephant in the room right for me it was the elephant in the room. Hold on a second. You are injecting we are
injecting now if you put back the slide on it if you please.
Um between 13.6 6 billion nanop particles for the Fiser vaccine to uh 46
for Mona and 50 billion for I think Astraenica and and J&J. Okay. So the
potential just just to understand the potential is um is to destroy 15 billion or or or billion cells.
That's [snorts] massive. Okay, that's a massive risk.
Not saying it's happening, okay? And that's absolutely not what's occurring, right? So just contextually, I I I want to point out to people that we have, you
know, a number of trillions of cells. So our cells number in the trillions um you know, in general.
Yeah. Yeah. Our our cell numbers are in the trillion, but that still is significant. Okay.
It's a very significant number. um it it's you know I think 14 million um nanop particles for fizer is about 18
square meters of endotellial cells okay okay that's that's that's enormous um so
so that was my first my first problem at the same time it was very clear that there was something else happen
happening um so the the the mode of action is is the center right every single cell that
will be um um contaminated by the vaccine or trans the term the technical term is transfected uh will be destroyed.
Okay. Now after that a [clears throat] lot of people I'm not the only one have been saying hold on a second what if you
know when you inject in the in in in the muscle uh or by mistake you know humans make a
lot of mistake and you know when you're like me a manufacturing guy you know quality and you know that when you repeat something if it's not if it's
human there's a certain level number percentage uh of of mistakes that will
occur. Well, the deltoid is highly v vascularized. Sometimes people have have
fat maybe. Sometimes um it it's not completely um out of this world to consider uh that
occasionally it hits a blood vessel either an artery or small artery or or a
small vein. Um and that part or all of the dose is injected intravascularly.
Okay. Now, yeah, exactly. I mean, you see there it's it's you have you have veins, you have vessels. It's it's, you
know, by definition very vascularized muscle. It requires a lot of blood to flow. So, um, and the
technique is is is, um, is not evident. There's a zone where you need to hit. There's an
angle you need to hit. There's people who have researched that if you're if you have obesity, you have problems getting in, you might actually do a a
subcutaneous injection where there's tons of vessels there.
So, so the the what I've been saying for over a year now is guys um you know can
we can can we consider this and investigate that because I'm pretty certain [snorts] that it's happening now I don't know how often but it's
happening it has to happen mistakes are made there's there's blood vessels etc
and uh and the fact that we have gone away from a an old
almost century old injection technique which was a the aspiration that most of us who are
above 50 have known when we were uh where doctors were injecting vaccines to us when we were kids. They would
aspirate. They would actually pull the plunger to see if they were in blood. if they had blood, drawn blood, they would stop, pull back and redo it somewhere else.
So, so I I'm I'm an actual physician and I have injected many things into people
um over the years including vaccines. Uh but you know, it was it's standard when we were taught to pull back on the syringe.
Okay. So, so, so you you see, I mean, there's always a tendency for modern doctors to think that the the ancient
doctors are stupid, but you know, if they've developed a technology like that, it makes sense. And I'm not the only one talking about that. Okay. Now I
there's a French um I participated to the the the the consulting board the uh
the shadow cons uh consulting scientific cons council board in in France where where I said that a year ago and a lot
of doctors said but Mark it happens very rarely once every 2,000 one every 10,000 and I was like it makes no sense from a
from a physiological standpoint it can't be that it has to You know, if if you have a map of LA or New York and you
throw darts at it, uh you're going to have um one chance out of five to hit a
road, right? The equivalent of a blood vessel. Okay? It's [snorts] going to be it's going to be smaller than that in a 3D environment because because there's
going to be less uh um you know, but but it's that's what I'm saying. It's it's impossible to be one in 10,000 and one
2,000. you know, see these pictures of these weddings and so forth in the Arab world. People take their guns and they shoot their guns in
the air and it's always seems harmless, but apparently Yeah. Sometimes you Yeah. you have people die.
Yeah. I mean, I I've heard that what goes up comes down and Yes. And people people have died from from, you know, paraphernalia from satellites, from guns
shot up in the air. We don't think about it that much. And I I frankly kind of amazed how infrequently it occurs, but it does happen that uh, you know, you
throw something up in the air and lands on somebody. So, but but the thing is I'm not talking about something that's that's that's um that's anecdotal. Uh
dentists, okay, dentists who are uh doing nerve blocks have 4% chance and in certain in some
cases 4% sometimes 11% chance of injecting intravascularly.
Okay, that's that's data. Okay. So might I mean you know maybe maybe the mouse is a bit more vascularized than the muscle but that's you you can argue against
that. Okay. But those are percentage points. We're not talking about one in 10,000. Okay. Now there is a number of
other um professions. Okay. Whereby exactly whereby you know plastic surgeons have had problems with fillers.
Okay. And they're getting by the way it was really interesting. they are getting very similar uh adverse events. Okay.
Very similar. Um and [clears throat] yeah, exactly. Mandular blocks is 11%.
Now I I I need to to to talk about Eric.
Eric Cross is a one of my readers. He's he's he's a
coach, a physical uh coach and he's a former bodybuilder um passionate about
uh biotech and stuff and he called me up um a few months ago and we talked about
the bullis theory and I I was telling I was struggling because most of the the medical profession was and including
nurses were telling me Mark you know you're nuts. It's it's that doesn't exist. This does not exist. What you're saying there is no no such thing as
accidental or inadvertent um intravenous or intra art uh arterial injection. And
I and I I frankly I beyond the the physiology the physiology which made a lot of sense I was having a lot of of
trouble. But then but then Eric in in a in a Zoom call like this, he's in New York, uh told me, "Mark, of course it
happens all the time." And I was like, "Okay, how come?" And he he talked about um something that happens to uh
bodybuilders who uh inject intramuscularly um steroids. It's called Trenov. And
what's really inter what's really interesting is um uh bodybuilders have developed a whole a whole protocol to
avoid that. So I would say they're they're much better than than WH. So they they build their own protocol. They
dilute it more. They aspirate, they inject slow very slowly, etc., etc. Um but what was really interesting is that
some researchers came up and despite aspiration one shot out of 50 is injected
intravenously or intravascularly. Now what what's really interesting with with Trenop is that you feel it immediately because
it's it's a vasoc constrictor and so if you've in injected it into a vein or an artery it's going to go to the to the to
to the the lungs. extremely quickly and you're gonna have a cough like crazy and you stop you can't breathe properly for
three minutes. Okay. So, so it's contrary to a doctor who injects the vaccines and you know says bye and you
never sees his patients for another six months or a year or or potentially never and would not know about anything. uh
the the injector who's self- injecting himself knows about uh about that fact
very very quickly and is very cognizant about it. So, so that's to me that was very interesting and it was indicative
that 2% with aspiration was very important and then after that I I had um
John Campbell who had a a professor from Denmark as you you know one thing to say to support what we're talking about is
that three countries have changed the injection protocol uh since since
January 2021. The first ones were Denmark which were probably the country that did uh um best or le let's say
least worse in in in this in this context but they they stopped in March April 2021. Hong Kong also changed as
well as um uh Germany changed this year in 2022 in February. Okay. Now, what's
really interesting in what what I'm telling you is that um if you have that and I' I've described that I'll describe
it a bit later. Um, but there there is a study that you were
about to show that that compared two two different types of vaccines and
actually did a deep dive analysis on the adverse events in 2015. And and what's
re very interesting is what they they compared was the flu vaccine. And the flu vaccine is not transfecting.
Okay? It's a protein. is broken down and it has a juvenox vaccine is transfecting.
Okay. And the results you could if you could show them the results were not the same.
I I just want to point out the small pox vaccine is the act is is an active attenuated virus is it not?
Exactly. And it's it's going to transact.
Yeah. So I you know for our our listener viewers um you know there are different vaccines. The standard flu vaccine is um
uh you know particulates that that were grown in I believe adnovirus and then extracted and injected. Um, and I think
some of the adnoviruses are there, but it's it's not intended um to kind of incorporate to our own um u genome the
same way that the mRNA naked. Um, no, it does it doesn't in it doesn't integrate into our genome, but it it
does integrate into some of our healthy cells. Um, so so the small pox does because it's it's it's a full virus
except it's it's it's attenuated. So it's not going to replicate but it's still going to enter cells. Um it still
has this spike etc. It's still going to do that. Now what's it's very important because it's for me we had we had it already precoid we had it we had the
solution in front of us. So you see the flu vaccine has zero severe adverse event. Of course if you do a bolus and we'll talk about the bolus about later.
If you if if you send a a let's say a swarm of particles uh with a
juvance to the heart, it's it's going to create an inflammation because that's what it's supposed to do. It's supposed to trigger an immune reaction. If you
can concentrate that immune reaction in one locus in one place, um it's it's going to it's going to create some
problems, but it's not going to be the same types of problems you would have with transfection because when you do the same
if you have that same swarm of particles and when they hit um the heart or or the
aorta or whatever and they start transfecting, then they are going to
um carpet bomb uh that that place. Literally, that's what's going to happen. They are going
to get in. Okay, this this zone is going to be like, you know, like like a target for the immune system. It's going to be
entirely destroyed, right? And that's the mechanism of harm of the vac of
these vaccines, right? So, so just to kind of cap, you know, encapsulate this a little bit, um, what we've said so far is that, um, vac
the the mRNA vaccine is is basically has the message for a spike protein. Uh, it's incorporated in
a, you know, kind of lipid nano particle. It's going to be injected supposed to sit in the muscle and destroy some of those muscle cells, but we don't really care about those because
they have, you know, a lot of muscle and so forth. and and send some spike protein out. Your immune system is going to see those things and then if it
identifies it somewhere else later on the coronairus it will have be prepped you know kind of like a police with a picture of the criminal in the
neighborhood it'll be able to catch him earlier than he would than he would otherwise. Now what your bolus theory is saying is all well and good is if that
were the you know something that happened 100.0% zero% of the time but in in point of fact there going to be some errors and there's going to be some leak
andorum some as you know aspiration in in the sense that that um I mean sorry injection without aspiration that some
of the injections are going to inadvertently hit um some of the circulatory system and veins are going to pull this back and then distribute
rather than have the the the mRNA vaccine isolated into kind of relatively you know mild inert muscle tissue going to be spread to other places and because
is vascular. It's going to go to the endothelial cells, the inner lining of your vasculature, including the heart.
Yeah, it's it's a bit more subtle than that. Let me let me tell you, everything is going to the vascular system. Okay.
Uh but but but the way it gets there is is there's there's two ways to get it.
There's a slow way with a very little percentage. The vascular system is intended is designed to distribute
oxygen, food, nutrients, etc. in an homogeneous way. It doesn't go to the heart in Okay. So, so let let me finish
on this one. It's a very important it's a very important point because it means that if you have a slow
um um leak into into the vascular system, it's going the immune system the
the vascular system is going to distribute the nano particles throughout the body. Okay. Of course, a big chunk
of it goes is into, you know, is shedded into the fcus into etc. [clears throat] But and and is destroyed. That's why
they put so much so many of these nanoparticles. Okay, they made huge numbers because very little transact.
So, so it gets it it it gets across and it's it's also not simultaneous, right?
So, it's going to hit here here and what's going to happen? Well, those cells are going to be destroyed by the immune system.
A message is going to be sent to the neighboring cell and the neighboring cell is going to duplicate and fill the gap.
Okay? It's going to happen hundreds of millions of times across the body. Not a problem. Okay? Now, if you have a bolus,
i.e. you get an intra um vascular injection and you push very quickly, not
slowly, okay? But quickly, what you're going to create is a sort of a a packets
of particles going to go through your your tubes, right, through vascular system and it's going to hit the heart. It's going to hit the brain. It's going to
get all sorts of places. By the way, that is the way drugs are delivered to organs. Okay, bullish delivery is the
way the pharmaceutical industry and you know doctors who want to who want to send um either a
Bose to the liver or to um or to the brain or for for a scan or or to the heart for other
Yeah. I'm going to backtrack a little bit. you know, we have a circulatory system and it sounds like it's just a circle and a lot of the pictures um uh
show that, you know, there's the blood going out, blood going, you know, out through the arteries, back through the veins, but we actually have a third system called the lymphatic system. And
for, you know, urban dwellers, uh, you know, I think we we notice some of the maybe we've seen some of these things.
We have the water that comes into our system under high pressure. That's the arterial system. Basically, you open the tap, hot and cold water run through and
then there's the drain that brings it back the sewage system which brings it back to some waste facility and so forth. But there is actually in in the urban areas there's a third system.
There's a passive runoff which is akin to the lymphatic system. Uh so if you have you know when it rains it doesn't go into the sewage system per se. It
goes in this passive runoff that goes into rivers and then it kind of gets recirculated through the rivers and uh aquifers and whatnot. That's a little bit more akin to the lymphatic system.
So we have um basically a third system that's you know ready to drain uh debris and whatnot. So if you do get injected and 100% winds up in the muscles and
some dead muscle cells as a result that's not going to go right into the venus system. It's going to go into the lymphatic system and then has filters which are you know kind of they're
filters. So they're going to take away some of the particulate work on that stuff and then bring before they do any of that before it gets back in your venus system and back to the circular
circular circulatory system it's going to be have been cleansed of debris.
So red out the thing that we know from the muscle from the the m the shoots the the shots from the injection into mice
uh from from the the Fiser data is that it doesn't transact very well into the muscle. there's a lot of it that goes
you know at least after after 48 hours at least 70% has gone and there's a fair chance that actually more of it is actually going to leak after that
because we don't have that data so so it doesn't transfaction is very hard I mean I've worked into in in cancer um the way
it was done it was through electroporation or with a or with a pressure gun um the only place where you have
pressure um is either at When you you actually get the aorta when you out out
just out of the heart, you have a lot of pressure there.
And and also when the capillaries start really becoming extremely narrow, you will naturally have, you know, sort of a a flow that sort of has has to fit in.
Um and that's exactly where where it's hitting. Now what is important is the fact that if
you have this bolus you're going to carpet bomb the endotilium and we'll see there are different areas where it can
do that depending on a different number of factors um and and and the immune system if it's
since it's done in a synchronous manner will actually just strip out the editium there. Mhm.
It'll just it'll be it'll be entirely destroyed just it will signal these cells to die and they will all die at
the same time and then a bit like when you you know when you burn yourself third degree well there's there's
there's no substitute there there's no way to cure it in you know the the term is omeostatis is
completely broken now if if if that's done on a massive scale and that's if for example if done in the arterial
system uh with so much pressure um there's there's two things that's going to
happen. One well the the the lining the protection the the protection lining is is destroyed.
So behind that you have what is called uh smooth muscle cells and they do a number of things. they hold up the they first of all they hold up the the artery
but also they produce uh uh they they produce um
calcification inhibitors. So if if they get in contact with the blood, they most likely decay and at one point uh you
will have either calcification or you you'll have um an anorism or an arterial
rupture. That's that's what we we see you know uh professor Burkart in Germany has has shown that happens a lot and it
happens not a week or two after the you know vaccination. It happens four or five months after the decay period takes
time. Okay. Uh that's that's when uh you have a highly
concentrated dose that goes into the the artery uh or the oral. Okay. If if for a
reason or another you need to understand also that there is a okay that's okay. You can go down on this. Um okay. So that's what happens right.
You can see this is exactly what I've described uh the evidence of immune attack on the endotal cells. Okay. So,
so there's the proof is there. What I've described is is is uh and if it were just one or two, it wouldn't do anything. You see it's massively done.
It's damaged. Okay, that can only happen with a bolus. Um now
what you need to understand before that there's a few slides after that Randall is that the these nanop particles are
protected so that um there they have a coating a PE coating um and um let's go
down let's go down a bit on that they have a PE coating and and that that in that stops yeah that's perfect this is
great so the you know when you you put all these particles into a a little vial I
think it's called and it's it's fat right and anybody who's put fat into water or soup or whatever has know that
they you know they aggregate and then and then it's useless so you want you want those nanoparticles to stay as as
individual almost like cells okay like microviruses or stuff like that and to do that they what they've done is
they've coded them with with uh PEG with polyatilico.
Okay. Uh which means that during u the first few instance maybe 10 seconds 20
seconds or 30 seconds the the they're not going to be able to transact.
Okay. So um and and by the way um if and
that's the reason actually otherwise you know everybody would have the same type of attacks that the the bodybuilders have right the bodybuilders don't have
coating it goes to the lungs immediately they feel it um if uh if it weren't for
um yeah if you have an intravenous injection it goes directly to the heart and to the lungs. Okay. If it weren't
for that for the PEG, most of the adverse events would be um
lung necrosis, pulmonary ambolism u and and potentially aorta. It would be just that and only
that. Um and that's not what we're seeing, right? So, so you see that that's a a graph I created, but fundamentally I'm I'm I'm guessing.
Okay, I haven't done it, but this is solid. I I think it's reasonable to think that after going through 110
kilometers of of capillaries, the PEG is gone. Okay, it's it's it's a fair it's most likely what's happening or at least
part of it is is gone. Um and and then it's if so it it starts hitting the aorta or it's not it's not
the coating is still there at the aorta and then it'll start hitting in a more diffuse uh diluted form the brain uh the
liver uh the heart uh and you'll have myocarditis paricard paricarditis or or
other problems like trombosis into um in into the deep vein introis into the brain etc. Okay.
Mhm.
If ever um if ever the injection is intraarterial, it's going to it's not going to go directly to the heart. It's going to go to the arm.
Okay. So, it's going to go to the arm.
Yeah. It's go go to the arm, the the the hand, if ever if if ever the artery is large enough, it's actually going down
um possibly in the muscle bit more and back up. So it it it'll it'll do a longer journey a much longer journey
with pressure going through the capillaries. So it'll be the PG will will will
last uh will be shorter. it will it will it will erode much faster and and then
when the uh nanop particles get to to the lungs they will transfect the lungs.
Okay. They will transfect the the capillaries. I have a that's not that's not what you're above. This is after how far.
Yes. This one.
Yeah. This one. This one. I have a friend I have a friend who who discovered he was he he was having
difficulty breathing he he felt you know it was and uh he lost 30% of his lungs
how do you do you have to have an intraarterial where actually an ear very early PEG
um erosion for that to happen. So that happens. It's very concentrated and it'll it'll you know it'll basically uh destroy um part of your lungs. Okay.
Now let's go let's continue on the process. So the first thing is arterial damage. The second thing is that people
need to understand um is is the trombosis. Why coagulation?
Now people have have gone I mean biologists are all going towards all sorts of very arcane and complex um theories. I think it's very very simple.
You know the the trigger to coagulation is endotellio disruption. If you cut yourself, it's because your endothelium
is damaged that in a grand in a in a insufficient way that the coagulation
factor u occurs. Now if it occurs here in the artery in the aorta or in the art
artery what is it what's going to happen? We all know from movies or for from medical school what that you can't
you can't clot an artery. It's impossible. You can't you can't you know it's you it's it it's just too much
pressure. It's too large and it's too it's too much pressure. So the coagulation factor is is just goes downstream.
You know the bigger the the damage the more coagulation factor goes and that explains trombosis strokes but also trombocytoenia.
The fact that you're um um U sorry red um um coagulation factor that trooytopia. Yeah, that's it.
Yeah, we say with thrombocyopenedia.
Yeah. Right. Now it also explains very very well uh the the famous whites uh
you know these these ribbons that we've been saying you know the these the the imbalmers have been taking out and ultra
surgeons you know on on live patients have been taking out some whiteish um
material from from from arteries now that would make sense that I can't prove but it makes in my
view utter sense in the is that you would have a decay of of a large part of the a
large part of the endothelium is destroyed. Then you have decay of both the the rest of the endothelium as well as the smooth muscle cells. Mhm.
[clears throat]
You're left out with elastin which is below behind which is like um yeah it's
it's jelly jelly and and and basically a lot of of of of coagulation factor
getting in as well which is not red by the way um which is yellowish or whitish um as well as as calcification.
Um and and so it it it make to me it makes a lot of sense that that's what's happening. Okay. So you're losing the endothelium, you're los then you're
decaying the smooth muscle cells are decaying. The whole thing is delletterious. Okay. Because it's not supposed to be in direct contact with
the blood. You have imu you have immune cells attacking it etc. And then you have anorisms. Uh no that's not it. So
don't that's that's a different that's a different part. So don't show that that you're getting ahead of yourself. Um so so that's the second thing trombosis.
Okay. Because of major endothelial damage um you have you you you have coagulation
that that occurs downstream in the venus system. Okay. Deep vein trombosis.
Third um mechanism of harm. Of course, if um if those um if for a reason or
another the um the peg remained uh better.
Okay, it it didn't sorry the peg wasn't eroded as fast. Okay, we we saw in that
chart I I showed earlier that the the danger zone is between the moment that
the PEG is eroded and the time where when the um the nanop
particles are fully diluted. Okay, there's there's a a window of opportunity. It lasts probably a minute.
Okay, maybe two, but fundamentally not very long. Okay. When when it's going to con it's going to transact in a
concentrated manner. Okay. And we know we we've discussed about the artery. But then if it goes downstream a bit more,
it can it can do the same thing in the brain. It can do the same thing in the heart. It can do the same thing in a con in a very concentrated way into all sorts of organs.
Um and then here you have there's a I have a slide about that. You have these these trees down down at the end. Um, Randall.
Yeah.
So, let me see if I can get this right one. But I I just want to give us a quick warning, a shout out that we maybe have about 10 12 15 minutes.
Yeah, but I'm almost through. I I'm I'm almost through this picture here.
Yeah. So, so fundamentally depending on the concentration okay of the hits you're going to have um
some inflammation some limited clotting okay the organs are not going to be destroyed you might have dysfunction
uh you might lose maybe the organ will regenerate maybe it won't like in the heart but you know these kids that have
mild myocarditis supposedly where they're they're they're between uh the the green the little smiley there that's
not smiley and and and the and the and the u and the orangey u um sign here
you you're going to have some clotting and some necrosis but but it's going to be dissim disseminated so it's not going
to it's not not going to kill the organ it's going to damage the organ and a lot of the organs are actually can actually
repair um but Then if if you have a a big dose and it's
highly concentrated, it's going to start hitting the organ and destroying bits of the organ. Just like I said about the
lungs, maybe 10%, maybe 20%, maybe 30%, maybe 100% of it. In which case, you have clotting
of all the capillaries, necrosis behind because there's no blood going to the cells and organ failure.
Right. Okay. And that explains so so going back the you see below um you know the the the the green smiley. No, hold on a second. Stay stay where you are.
Here you see um when it's light myocarditis, he epatitis, pulmonary ambolism. When it's a bit more, you'll
have ant intestinal disorders, arrhythmia, hormonal disorders, type 1 diabetes, pulmonary necrosis, and then
organ failure is death for a lot of them. or you know I have a friend who's who's got gay bladder gallbladder failure deep vein trombosis heart
attacks intestinal failure kidney failure liver failure okay all of what we're seeing we're all seeing that right
it's just a question of where does that bolus go right and that's that's the that's the thing that you were showing
earlier that's p purely a a bad luck okay now the the fourth mechanism of arm is in my you fascinating.
Um, and it's tied to a sort of a um
medium hits or or not not too serious hit um of blood to tissue barriers.
Um so myocarditis would typically be that. Okay.
um the there's a Japanese study that showed that myocarditis
is going to is actually related often to a higher permeability of the blood
tissue barrier. So basically uh of the sorry the yeah the blood tissue the blood heart barrier. Okay. So in um so
the endothelial the endotilium is be is is no longer tight and it's going to let
in um elements that are that that are going to be inflammatory. Okay. M
now it's the heart is we we know about it's it's not it's not very it's it's not going to give you a specific beyond
beyond the temporary uh period where where you're going to have myocarditis and and of course that can kill you long term.
What's really interesting is the leakage of blood tissue barriers is linked or
you know multiple diseases are linked to leakages of blood tissue barriers.
So let me let me run you through there's two ways that leak is dangerous.
One is because it lets in stuff material that's not supposed to be there. It
could be um toxins like albamine or stuff like that or it could be um immune cells that are not supposed to go there.
Okay, there are plenty of places in the in in the body where um notably the reproductive system where you don't want the immune system to be. And the other
aspect is is not letting so that's letting in um you know somebody you know a criminal
um and and the other thing is letting out uh your kids too early basically. So basically it's it's you open up the
doors and you have your your toddler who's going outside. Okay. So running in the street and and what when you start looking if
you go back to that chart you were showing there's a number of illnesses that are massive okay uh tied to that
now first the the leak in the blood brain barrier I wrote a piece on my co mythbuster substack I encourage people
to go and see it it is it is fascinating I wrote it as you know it was work in process so
if you you know those blood The BL brain barrier is highly sophisticated. It's probably the tightest barrier we have.
And there's a reason it's there. Okay.
If you open it up, if you have leaks, it's been proven that depending depending on the area. I'm going to get my I'm going to get my brain.
Okay. I'm going to get my brain. uh depending on where um where you get hit. Here you you have
the white and gray matter. If you have a leak in in the BBB there, it's Alzheimer's.
Okay? If you have a leak in the basil ganglia, I'm not so sure where it is to be honest with you, but around here.
Okay, it's basin's etc etc. there is a a direct correlation
between leak location and disease specification.
So, in in other words, it's not it's it's most likely not the the the fact that you're having aluminium or that
that's the problem, you know, or or it's the fact that you're letting in material uh inside the brain and your immune
system cannot correct for that because it's not supposed to be there.
Not supposed to be there. Yeah. And we have we have enclosed parts of our body like the eyeballs and uh in in our joints and so forth. And when those
things do get exposed, they can be, you know, big issues. The immune system can cause problems.
So what I'm saying is, what I'm saying is these vaccines and other vaccines, MMR, yellow fever, small pox,
chickenpox, all the attenuated vac virus viruses, vaccines,
if if they're poorly injected, if they're accidentally injected
intravenously with a bolus, can create dementia and stuff like that.
Now the let me finish because it's it's so you you take this that's the brain.
You go to the reproductive system. Okay.
The reproductive system of the male. We have two blood tissue barriers. One is is the is the the blood testice barrier.
The other one is the blood epidal barrier. Women have the blood follicle barriers.
Um [clears throat] having having worked on HTH because of the vaccines I was uh working the company I was working for was targeting
HT the testice is a place where you have a H ch is is uh is actually expressed so
that telomeres are were actually repaired.
Um but the immune system might consider uh your your sperm as actually foreign material
because of that. And guess what? Well, sperm count is down in in in Israel and fertility is down. Okay, continue.
Same thing. Placenta is an is a it's it's also a blood to placenta barrier. You have the blood milk barrier also.
all those accidents with kids, right, that are being that are being leaky and and and women have have, you know, dark
almost bloody milk looking milk that is most likely toxic. I mean, there's a reason these barriers are there.
Absolutely. So, I'm I'm gonna just ask you to do two minutes to to wrap up.
Okay. So and and and you continue all the the the the bits u all the glands all the hormonal glands.
Okay. The um are doing the same thing.
Okay. They they if you if you let them open what do you do? You open up the door to hormones. So people have too much hormones.
So they start having uh you have the you have many many issues with of course with with menstrual cycles.
Okay. Um, you you also have the blood bone marrow barrier. Now, that's a fantastic one because the bone marrow
does two things. It does immune cells and red cells. Okay. So, what what happens if you starts um releasing red cells too? Too too many. It's not
uncontrolled. You have too many. My best friend has what? He's got a comp um uh disease called vakas disease. it's
actually having too many um red blood cells. It's not that the bone marrow is producing too many of it. It's that the
the blood bone marrow barrier is releasing too many of it. And that's true for the immune system.
Now guess what? You know all these people who are having uh vedes
which is vaccine induced uh um uh what is it called? Immune deficiency.
Okay. Acquired immune deficiency. It it's basically if if if there are um immature
um immune cells in the bone marrow, if you release them, they will never mature
by the time. So you might have basically either I depending on how your bone marrow is hit, you might have a period
of time of a few weeks when your immune system is weak because your bone marrow is is is in multiple places. it it most likely not get everywhere.
So, let's let's say let's say I I'm going to try to have have to cut you off because we're going to stop under an hour. Um, but you're in charge of the
world vaccine so forth, but what what are your quick recommendations at this point? We're not going to go retroactively.
Very simple. It's it's it's it's what the the Danish have done. Okay. So, you you do aspiration. You you tell you tell you tell people this can kill people.
Okay. You tell this is serious. So, first of all, the method where they hit.
Okay. They're not supposed to they're not supposed to do that. If ever people are fat, they need to have longer needles.
So, is this exclusive to the mRNA type factor?
No. No. This is true for MMR too. So, aspiration needs to come back. Not only aspiration, but also slow plunger.
This needs to be done over two or three minutes, not in a second because you're creating a bolus. creating is a bolis is
the is the real problem. Okay, those are very I mean go and see what the the the the bodybuilders are doing.
I wrote a piece on that. So um is there a you know I like to think about verifiable falsifiable is there a way to
verify your theory aside from let's just stipulate that everything you say is correct that you know mistakes can be made things can be aspirated but in very
brief u time like a minute 30 seconds is there a way to figure out whether your theory is correct okay so so first of all when apparently
according to professor tobby in in Denmark myocarditis fell 60% % when they started versus Norway.
That's interesting. I'd like to see that.
Okay. That I didn't find I didn't find the study, but that's what he said. Okay. Fair enough.
Um I I I couldn't find the study. If you find it, send it to me. But fundamentally, that's that's the first point. The second point is the fact that
it it's it's it's it's um it's a clinical uh truth. It happens. Okay.
This this happens with injection. No, I I I after that the the mode of action of
having NKs or T-C cells attacking transfected cells has has been proven over and over and over again. That's a certainty.
All right. So, I'm going to have to cut you off there because um I'm trying to stay for an hour that uh helps us get up
um uh on the networks better. But I'm going to uh you know let let keep keep you open for answering questions uh when
they come in. I'm going to end the broadcast now. Thank you so much, Mark.
I appreciate everything you've done and I appreciate you're spending the time with us.