Okay, welcome everyone. Hello again. So we're up to session number three, I think it is.
What I'm going to do this time, which I should have done last time, and you all witnessed
the problems of that, I didn't open in prayer. And we need to acknowledge that, you know,
the prince of the power of the air doesn't particularly like what it is we're trying
to say, but God has got above all. And so I want to commit this time to him that it's
his word that comes through and that his purposes that are fulfilled. So, so dear Lord, we just
we just come before you now we thank you for your promises that we're two or three are
gathered in your name that you are here we thank you that your presence is the presence
that will be over this time and will be governing and controlling this time, that it's what
you would be delivered, you would have delivered that is delivered, and that be a blessing
to all those years to all those who receive. So just your blessings on this time we commit
it to you. We thank you in Jesus name. Amen. All right, so I'm going to pick up I'm actually
going to go back into that.
Change my screen. Choose virtual background. Where are the rest?
Robin, are you there? We seem to have lost you.
Robin?
Oh no, the raptures happened.
She is obviously going to be jumping on to the other platform she said she had available.
So we'll just give her a few moments to do that.
Here she is.
That didn't take long did it?
We gave it you'd be back soon.
Okay, alternative system is up and running. And my goodness me this is ridiculous isn't it but anyway.
Okay, so, so I'm going to throw on now, the, the slideshow from, from what we started last
time I'll whiz through the bits that you've already had but I want to get into the things
that you didn't have. So I was talking about. So last time we were talking about the vaccinations.
Okay. And about the things to consider with any medications. I went into the question
of whether these were necessary, and into the background of all of that. Then this very
key thing about immunity that the World Health Organization has changed our definition of
immunity. The issue of the virus mutations that it is natural and normal for viruses
to mutate and they will especially do so when they are under pressure, which is what we've
been doing by vaccinating. So these are the things that I couldn't get to you last time
but I want you to get this and understand because this isn't just relevant to COVID.
This is relevant to a whole question of health in the background so now we're going to launch
into some teaching about the immune system and how the immune system works.
So our blood cells, all our blood cells are made initially first levels in the
bone marrow. So the blood stem cell in the bone marrow is where things kick off.
And there are two types of blood cells. There are your myeloid. So these are the ones that
then and then the lymphoid. So the myeloid are the ones as you can see from the diagram
that come down into your red blood cells and then across into white blood cells particular
types of white blood cells called the granular blood cells. That's why they're called myeloid
and the platelets and then those myeloblasts which are ones that contain granules
then break down into your basophils, neutrophils, eosinophils and monocytes.
So Robyn are we meant to be having something up on the screen here? We've got nothing to look at at the moment.
I must have forgotten. It's come back into, I threw it up on there and I forgot to hit.
Let me come, oops, I'll have to escape from that. Yep. Oh, doesn't want me to escape.
All right. Are you able to do this on your end or I need to do this from my end?
It's not letting me escape now. I don't know why. Screen share.
Are you able to screen share me from your end?
Elyse, you're muted, Elyse.
Elyse, are you muted?
Thank you.
No, I can't do it on my end.
Sorry, Robin.
But you can definitely do it on your end.
And I will have to remind me again how I do this.
So down the bottom, there's a share screen.
If you go down to share screen.
Sorry.
But it's disabled.
Mine is disabled.
So you need to let me in to do that.
I have said I'll say multiple there, see if that makes a difference.
Has that helped?
Sorry.
Let's see if that gives it to us.
Are you seeing that?
I am screen sharing.
Yes.
Okay.
So hopefully then that will mean that you are now going to get this.
So I'm going to go to the next slide.
Right.
That should be right now.
You've got it now?
Yes, we have.
Thank you, Robin.
All right.
So we'll whizz through again that first bit.
So this was talking about any medication we consider.
Is it necessary?
Is it safe?
Is it efficacious?
And then we were starting to apply that to the question of COVID
vaccines and basically saying it's simply not necessary for all of
these reasons that you've got in your slides.
So the first thing that we did was we looked at the definition of
immunity.
And I think the health organization has literally changed the
definition of immunity.
Whereas before natural immunity was important.
Post-infectious immunity was important.
Now immunity only counts if it's what they call herd immunity from how
many people have been vaccinated.
And that assumes two things that assumes that the vaccines are
actually actually effective.
In creating immunity.
Whereas in fact,
the trials show that native immunity is effective and it is durable as
in it lasts.
So we're going to go in and then I've talked about the question of
virus mutations.
So now I want to go into talking a little bit about the blood cells.
So you get an understanding of what,
as we go through the pictures of how the vaccines are working and why
we're getting problems from them,
you'll have an idea of what I mean by the different cells.
So the bone marrow is where all our cells begin.
And we, we have what we call the, the hematopoietic blood stem cells.
So these are the beginning cells,
the precursor cells and they're in the bone marrow and these cells is
really basic background.
One cell then splits and it starts to what we call differentiate.
So this is a, this precursor cell primordial cell can become a whole heap
of different things,
according to the factors that are going on around it.
So it's got DNA that'll enable us enable bits to be switched on,
switched off. So it'll become one thing. It'll become another thing,
depending on what the requirements are at the time,
what the pressures are at the time.
So we have the myeloid line and the lymphoid line.
So the myeloid line,
these ones become the red blood cells and the myeloblasts.
So all the myeloblast category that you see there have granules that
contain different things.
So they're granular and then the platelets.
So all of those come from the same precursor,
which is why if someone's got a bone marrow disease,
you will tend to see problems in the same parts of the bone marrow.
If they've got a platelet problem,
they'll usually have a problem also with,
with some of the myeloblasts or a problem with the red blood cells.
So your different myeloblasts, your basophils, your neutrophils,
your eosinophils, your monocytes.
And I won't this time talk into the function of all of what they do.
The important one really from the point of view is as we start talking
through more about COVID and more about the vaccines,
it's going to be your monocytes because the monocytes later on,
mono one, because they've got one nucleus,
whereas you look at the other ones, they've got, you know,
multiple or low nuclei.
So the monocytes are single nucleus,
but the monocytes differentiate further into other things called
macrophages.
And we'll talk about them a bit later and show you those creatures a bit
later.
In the lymphoid cells,
these are the precursors for your lymphocytes and you've probably heard
about lymphocytes, so white blood cells.
So both the myeloids and the lymphocytes are regarded as white blood
cells and your red blood cells,
where we all know our red blood cells and they're red because they carry
hemoglobin that carries oxygen.
So there's no hemoglobin,
no oxygen carrying capacity in the white blood cells.
They are all immune acting.
Red blood cells don't operate at all in the immune system.
They can be affected by it, but they don't operate in it.
So your lymphoid stem cells then come down to the lymphoblast,
which is your more specific precursor form.
And that divides into these three types, your T cells.
And that's not because they're shaped like a T.
I'll come to why they're called T.
T-cells and your B-cells and your natural killer cells.
So remember those, natural killer cells,
they are very important.
So then we come to, this shows why they're called B-cells,
why they're called T-cells.
Your B-cells are made,
they stay in the bone marrow until they are mature.
So it looks like they've come from the bone marrow.
The precursors of everything comes from the bone marrow,
but they're not released from the bone marrow
until they are mature.
And then once they're out, they can be activated.
Once they're activated,
then they are able to be making the antibodies,
which is what the B-cells do.
Your T-cells from the precursor form
go straight into the thymus gland.
So outside of the bone marrow,
and then they start to mature
into the different types of T-cells.
And there are quite a few different types of T-cells.
Depending on the signals that come,
you'll see here there are different signals,
interleukin-7, a TCR signal, and so on.
Depending on the different signals,
exactly how that T-cell will turn out,
which type of T-cell it turns into.
But it's all about signaling.
So you've got B-cells and you've got T-cells.
So again, remember that difference
when we come to talking and seeing how the vaccines work.
So here we see a little more of the interaction
of your B-cells and your T-cells.
So here's your B-cell, and you can see it in blue.
They've nicely colored the B-cell in blue for you.
And coming along to the B-cell,
the B-cell's got its receptors sticking out,
is what's called an antigen.
So what an antigen is, is an immune irritant, if you like.
It's typically part of a bacteria or a virus,
can be a toxin, can be a protein, can be a lot of things.
But something that the immune system doesn't like
and it regards as a problem.
So the antigen comes along,
sticks on the receptor of the B-cell,
at the same time as another receptor of the B-cell
is getting a message from the helper T-cell.
So basically the helper T-cell is coming along
also with an antigen, and it's docking to the B-cell
and saying, guys, need you to get activated,
get your act together.
The T-cell makes some interleukin,
meaning messaging system between white blood cells.
Leukin stands for your white blood cells,
so inter, between white blood cells.
So the T-helper cell is making messengers
to go to the B-cell, as well as docking to it and saying,
okay, wake up B-cell, do something.
And so the B-cell then differentiates
into two different types of B-cells.
The memory B-cell, and this is the one that then goes away
and remembers what has happened here.
And then the active, what's called plasma cell
that makes the antibodies.
So as you can see, even just from that little diagram,
there's quite a bit that goes on in the process
before we get to antibody production.
But what's the only thing that we measure
when we're looking for so-called vaccine-induced immunity?
The antibody production.
So we don't look at the T-cells, the T-cell activation,
the memory B-cells, all we do is measure
how much antibodies have been made.
So here's another way the T-cells work.
And I mentioned before the monocytes.
So the monocytes move across and they differentiate
into what we call macrophages or phagocytes.
So the phagocytes eat things.
So the best analogy is Pac-Man.
You all know the game Pac-Man.
And in the Pac-Man, these things,
these Pac-Men go around the place and eat things up.
And so what happens here is that the monocytes
become the active phagocytes, the Pac-Men,
and they are eating things up.
But the T, here's a T-helper cell again.
It is activating things.
It comes along to the phagocyte and says,
here you are, guys, here's the antigen,
here's the thing that's a problem, get active for us.
And so here you see the picture of the macrophage,
the phagocyte eating the problem, eating the virus.
Okay, so that's two actions.
Now, again, that's not an action
that gets either activated by your vaccines
or is measured in your vaccines.
The only thing that we measure in seeing
has the vaccine so-called been effective
is the antibody production.
What's the third way that these interact
or that think the T-cells work?
It's just really about how the T-cells work
to help everything.
Your third way is that your, remember I mentioned earlier,
the natural killer cells.
So we've got T-helper cells.
We've also got T-suppressor cells,
which I'm not showing here,
which will switch something off
if it's getting too overactive.
But here we've got the killer T-cells,
the cytotoxic T-cells, your natural killer cells,
the cells that just go along and.
gobble stuff up, kill things up. So here's your killer T cell, sending a message across again,
coming into the infected cell, which has got antigen in it, the T cell reads that it's got a
problem. So this killer T cell then makes stuff, perforin, the cytosine killing stuff to kill that
cell. So it isn't using, note this, it is not using the antibodies that the B cell has made.
It's not using the macrophages that have been activated. It itself, by itself,
is killing infected cells, natural killer cells, part of the T cell family. These are not measured
at all when we're looking at the how effective or our effective measures has the vaccine switched on
on immunity. So here's another picture showing how these T cells will activate the B cells. So
don't worry about all the PAX5 and the blimps and the XBPs, don't need to worry about any of that.
But here's the overall picture. So the dendritic cell, these again relates, they derive from
the monocytes. You can see these cells have got lots of arms, if you like. So these cells are
reaching out and grabbing stuff and presenting it all the time. So they're out there in the
tissues, grabbing things. So the dendritic cell has found something. Your CD4, your T helper cell
is saying, yep, we've got a deal. It's taking it all to the B cell, which at this point,
naive, meaning it was basically asleep and they switch it on. It turns into a plasma cell,
which makes all these antibodies. It goes into, so the germinal sensor. So this is where we talk
about in the lymph node and we get this, this concentration of these B cells. But anyway,
it gets activated and it makes all these plasma cells with all these different types of antibodies,
but it also makes a line of memory B cells. So later for those memory B cells to get reactivated,
if we come into contact with something like that again, again, we need the CD4 T helper cell.
And yet the only thing that we measure post-vaccination is antibody production in your
B cells. Is that making sense? There's a whole arm of the immune system that we're totally ignoring.
We're forgetting. And this arm of the immune cell, the T cells are essential for healthy
immune system function. And so you'll remember that for next week, when we start talking about
your vaccine side effects of what the vaccines are doing to our T cells. So T cells, absolutely
crucial for the activation of the B cells, for the B cells to make the antibodies, and then to
convert your memory to your cells later to activate them, to make antibodies again, when something
else happens. So there's our B cells. So here we are again, looking at this difference only now,
we're kind of looking on the cell surface. So APC, this is your antigen presenting cells. So
these are the dendritic cells that I spoke of earlier, all the phagocytes. So these cells
that have kind of grabbed something and gone along into the system and said, Hey guys, here's this
problem. So here's your cytotoxic T cell on its own, recognizing the cell's got a problem and
killing it. So it's not using any antibodies. It's not doing anything else. It does it on its own.
Then we've got the antigen presenting cell coming along to the B cells. And this doesn't actually
show the T cell activating it, but it should be putting the T cell in the picture there as well.
But the T cell then activates that B cell and it makes the antibodies. So see the antibodies work
by creating kind of like a claw structure that surrounds the thing. Once it's got this claw
structure that surrounds the thing, it inactivates it. And then depending on where it is or what it
is, several things can happen that can be eaten by the macrophages. It can be dealt with by the
rest of the immune system, but it basically blocks its action. So T cells can work on their own,
depending on the type, or they will activate your B cells and the B cells then make the antibodies.
But there's this whole immune system coming together. Now that was talking about immune
system in the blood. And this is where the vaccines go. They go straight into our bloodstream.
They totally forget that in fact, the first time of our immune system is not in the bloodstream,
it's in the mucosa. So what do I mean by that? I mean, the lining of our mouth and our nose,
the lining of our airways, the lining of our gut, and for women, the cervical epithelium,
you know, vagina. So all of these in mucosa is internal skin, if you like. Now we do have a
degree of immunity on the external skin, but nothing like it.
internal. So the internal skin, and what you see on this
internal skin, if you like, is a whole other set of immune
protection that kicks in before we talk about what's going on in
bloodstream. So so let's have a look in the mouth. So stuck
antigens cross the oral epithelium and what's sitting
here, a T cell. So the T regulatory cells in particular,
sitting there to control to keep what's going on in the mouth
under control. And our oral bacteria are very dependent on
two particular things. They're dependent, we'll come back to
this when I talk about breathing. They're dependent on
how we breathe, and they're dependent on what we eat. So our
oral bacteria affect things. Our airway epithelium, so the lining
of the airway. So all of these are single cell layers. So all
of our intestinal internal lion linings are single cell layers.
Whereas our external skin is multiple layers, for obvious
reasons, it's got a lot more to protect that it's got to protect
against. So again, we look in the airway, we won't bother
about all those other things there first, but we see here's
our dendritic cell, our cell that's sticking out its bits to
find stuff. My cells are type of eosinophil, it's a tissue allergy
cell. So we've got a lot of those in the airway allergy cells
through the airways. Here's our T cells that then connect to our
B cells. So we've got two main types here, here, they're
talking about the Th2. So Th, we have two arms, this is a quite
separate lecture altogether, really, Th1 and Th2. So the Th2
are the types that will activate your B cells. Then your T
regulatory cells, these are the ones that just keep everybody
under control. Cervical epithelium, again, this idea of
here's your pathogen, your virus, your whatever, here's
your dendritic cell again. So the same critter we have over
there, here's our dendritic cell, sticking its way out
sampling what's going on, sending the message to the T
cell. So the gut is a little more complex, there's a lot of
stuff going on in the gut. And what this shows you here is that
not just and we have this to a degree in the airway and the
cervical epithelium as well. So not just do we have the cell
lining, but above that cell lining is a very thick layer of
mucus. Now we know if we've got something going on up in the
nose of the mouth, we get mucus, right? And we think it's a bad
thing. But the mucus layer is key protection to the underlying
layer, an absolute key protection. And above that
mucus layer, what have we got, we've got a layer of other
bacteria. So this is where we come again, I'll be talking on
this later, to the whole issue of what we call the gut
associated lymphoid tissue. Depending on who you talk to
which paper you read, between 70 and 80% of our entire immune
system lines the gut. And that's where it's sitting. It's sitting
in a layer above the mucus above the intestinal cells. So if we're
giving a vaccine to protect against something that is going
to come, as almost everything does except an illness that has
come via injection, right, like from a mosquito, that's the only
way you're going to get those. Everything else we get comes
via the mouth or via the gut, and most of it via the gut. So
God in his wisdom has given us multiple layers of defence for
our gut before we come anywhere near the question of B cells
needing to make antibodies. So we've got our protective gut
microbes, and you know, we're going to be talking an awful lot
more about them. We've got our mucus layer. And there again is
a whole heap to do with that mucus layer. Inside that mucus
layer, there is a non specific but very important type of
antibody called secretory IgA. And I'll come back to that a
little bit later. But that's a non specific secretory IgA. Then
under that, here's our dendritic cells sticking its head out kind
of saying what's going on up here, we've got all these other
microbial sensors coming into the gut wall, this goblet cell
over here, this makes mucus. So this is what the job of the
goblet cell is, is to make the mucus the protective mucus
layer. So here's our dendritic cell, it's brought something in
and it talks first to the T cells. Here's your Th1 cell. So
the Th1 is linked to this first time of the immune system, your
Th2 cells are the ones that come along and activate your B cells,
your Tregs, Th17 are the regulatory cells. So they're the
ones that keep things settled.
down. And then of course, as I mentioned earlier, the B cells
can be activated. This one's a bit hard to see, but I thought
I'd keep it in just to give you an idea again, we can skip it
fairly quickly. But this idea that it isn't just about your B
cells, and these are the activated lymphocytes down the
bottom. Here's your NK cells, these are still T cells, this
still isn't even talking, we still haven't got to the B
cells. Okay, all of this goes on before we get to the B cells.
So it's very complex. So looking again at the gut, all of these
layers in the gut. So mucosal lining and our bacteria is on
the top of that. Here's our goblet cell, here's our
dendritic cell, which is grabbing some stuff and sending
some messengers out because of it. Here's stuff that has come
through that is taking activating our T cells, so it
goes into action. Here's some other stuff coming in that is
activated our macrophage. Here's another T cell being
activated. Here's a neutrophil, which don't make antibodies,
neutrophils are nonspecific, also being activated. Again, all
of this before we get anywhere near the B cells that are making
the antibodies that we measure post vaccination to say that
we've done something. And that again, is you're all still
there. Yeah. So here again, your intestinal lining. And under
that, we've got our green macrophages, these are your
pacman. We've got our star like dendritic cells that are
catching stuff. We've got a little type two lymphoid cells,
the little red ones that are going to go and talk to the B
cells. And all of this happens and it talks to the nervous
system. And again, we'll talk about that later when we talk
about the gut brain access. So now I'm going to talk about how
the B cells fit into this after we've talked about all the rest
of this. So here's a mucosal lining here, our dendritic
cells and the M cells that sense and send it to the dendritic
cells. A thing has come in and it activates first our T cells.
So this is actually talking about this has actually come
into the lymph node. So this is a lymph node now, which are in a
little bit, right? They're not right at the surface, they're in
a little bit. So this stuff is all now coming to the lymph
node. And first it talks to the T cells. So the T cells are on
the outside, and then the T cells talk into the B cells. And
the B cells start to make first they make IgA. Because IgA is
the antibody that comes back and you see it here over the other
side, that coats the intestinal lining and the mucosal lining of
the respiratory tract. So it coats these places with a
protective coat over the top of it of antibodies. But that only
happens after these messaging systems, and your IgA goes
through the bloodstream. So all of this has happened before it
hits the bloodstream. So then we get to the B cell that gets
activated to be a plasma cell and it starts making more stuff.
Then we get our activation of our Th2 that's interacting with
all of that and we get more stuff. So again, you see, there's
this big difference between what happens first off, and what
happens secondly, there's a lot of activity back over this side
before we get to our antibody production. I know this one's
blurry again, but the reason I'm keeping this one in is back over
here. So Pius patches are the little lymph nodes inside under
the gut lining. And here's your plasma cells being activated,
making stuff into the bloodstream, making their
antibodies. Here's our interaction with our T cells, our
Tregs, our Th1, Th2, T17, all activating the B cells making
stuff happen. But back over here, I just kept this in to show
you retinoic acid. Retinoic acid is vitamin A. So vitamin A is
crucial for the health of our mucosal immunity. And you will
have heard me listen, list vitamin A back in the treatments
for COVID. Why? Because vitamin A is crucial for the mucosal
immunity and for the production of IgA. So retinoic acid,
vitamin A, and here it is working, you know, particularly
around your dendritic cells. But vitamin A is crucial. And it's
crucial because there are particular receptors called
G-protein receptors that need vitamin A. So we must have good
vitamin A levels. Old fashioned cod liver oil, as I keep saying,
good old fashioned cod liver oil. So still with our
intestinal lumen, so here we are.
Here's a sensing cell, our M cell, talking to our dendritic cell, starts to send messages,
your interleukin, your messaging systems coming into your other cells. This all travels into the
lymph node and that's where we got that activation. We've got your T cells on the outside and the B
cells on the inside. That starts to make your T cells now that are activated and ready and going
to get the message, goes around the system. And this is two-way streets. This comes in,
so it has to come in from the gut lining. All of these messages from all of this comes in from the
gut lining into the lymph node and then the B cells make their stuff, the C cells get activated
and it goes out through the bloodstream to go where it needs to go. But a lot of activity
on the mucosal layers way before we get to the lymph node, way before we get to the bloodstream.
I'm just making sure you've really got this idea. Here it is again, this is showing your
lymphoid, the places of your mucosal immunity all the way through, right from the mouth,
all the way through the lungs, all the way through the gut, all the way through it,
through the uterus, all through here. Same kind of concept everywhere, that you've got your
dendritic cells, your M cells that are directly linked with the environment, attaching to your
dendritic cells. They then carry it through your messaging system, kicks off into place
through the lymph node, your T cells get activated. They tell the B cells back here to make stuff
and your antibodies get made. An IGA is your mucosal one that first gets made to protect
the mucosal lining. Again, summarising that upper tract, upper respiratory, lower respiratory,
gastrointestinal, urogenital, but also in the glands, your messaging comes in, the B cells
make your IGA to protect that and the secretory IGA is what then is coming out.
So before I, I'm going to escape that if it'll let me. Okay.
We'll come back into, into there. Alright, so everyone's with me on to there. You've got that?
Yeah. That's all okay.
Clear as mud.
Clear as mud. Alright. Do I need to, can someone throw me a question or something to see what
don't you quite get that I need to.
I'm going to watch the replay and go very slowly through it. That was new information for me. So,
yeah, just lots, lots to take in. Amazing how God has made us though. Absolutely amazing.
It is amazing how, how God made us. It absolutely is. That's right. So I've gone in,
you're now seeing my worship initiating volume 25 sitting there, aren't you? I'm trying to make
this stop doing that. Let me turn, stop share. Right now I've got you guys back. Sorry about
that. Now you know what I listened to, don't you? Okay. So, but the, the summary version,
just what I want you to grasp, and I don't expect you to turn around and give lectures on this,
but I wanted to show you when, that when we simplify this down and try and say, all you've
got to do is have a vaccine and measure antibodies and you're immune. Can you see now looking at that
how absolutely ludicrous that is? Yeah. Does that make sense to everyone now
that we simply can't just say that we're going to stick an injection into someone
and measure the antibodies and say, therefore they're immune.
Right. So, so that's, that's, that's the key thing I want you to get out of that.
But the other key thing, the second key thing that I really want you to grasp out of that
is that the mucosal immunity, what is happening on the lining of our mouth,
our respiratory tract, our gut, our vagina is in fact probably more important
because that's the entry point where everything comes in. All the action starts there.
The key thing that I didn't say, the process of antibody production
when something comes into the system takes four days.
So think that through for a second. If your mucosal immune immune system isn't working,
you're sitting there waiting for the four days for your antibodies to kick in.
So if you'd made, if you've made your immune system dependent on the antibodies,
which is what you do by vaccination,
you've made your immune system dependent on the antibodies, which is what you do by vaccination.
vaccinating because the vaccines switch off the first time
in the immune system.
The virus or bacteria, or whatever else
it is that you've tried to protect yourself against,
actually can walk in and have four days happy holiday
while you are getting your act together before your body
can make the antibodies.
Whereas if our immune system, our mucosal immune system
is working, it's like stopping it at the pass, right?
We stop it before it can get in,
or we stop it before it gets really to the bloodstream.
With all of these things that God has designed us
to be protective, then the antibodies,
all they've got to do is come in and mop up afterwards.
Because we've already activated,
we've already got our secretory IgA working
because it's already there.
Our mucosal system is already happy.
We've already got the right bacteria sitting there
to do battle with the other stuff before it even gets in.
Our T cells are working well because our immune system
is well balanced in the background.
We've got good levels of vitamin A,
so the IgA can be made well and so on and so on.
So there is so much that God has really put
in our mucosal immune system before we start thinking
about a vaccine injection to activate
the antibody production, okay?
So, all right.
And I apologise for some reason when I can put slideshow
because I'm needing, for some reason,
when I put slideshow in comment to what's being put in here,
the computer isn't making it a full slideshow.
It's giving you the slide and then the other alongside,
and I don't know why it wants to do that,
but it does want to do that.
So now I'll skip on down.
The next section I want to come into,
so we've just talked about all of that
for the immune system.
Next bit I want to get down to,
so I started to talk last time on the different vaccine types.
So now we'll see how, remembering what we spoke about
on the immune system, how is this relevant
to how our immune system works?
Okay, so, oops, sorry,
I've got to put this back onto SlideShare, sorry.
Let me come back to here and we'll SlideShare again.
So ScreenShare, okay.
Okay, so vaccine types.
So this is weird because on my main screen,
I have got it as a total screen share, as a total slide,
but on the other, it's giving you half and half.
So I don't know why it's doing that.
So four main types of vaccines,
the whole virus vaccine,
the protein subunit vaccine,
and the protein subunit vaccine.
The protein subunit vaccine,
the viral, which means we take part of it,
the viral vector where we've used a viral,
like a mosquito, if you like, to deliver it,
and then the nucleic acid vaccines.
Okay, so those are your different types.
And so now let's have a look at that here.
And can I make that bigger?
It's good on my screen.
All right, so over,
so this is our purification
where we come to the protein subunit type.
So they've started up here,
they've taken a virus, a bacteria, or whatever,
and have broken it down to the subunit,
and they just inject that subunit.
And that subunit then comes in and activates our system.
So that's how they've done that one.
So then when we come into our,
so this is another one working on the same thing.
So this is where we've got,
this is coming to our sort of whole vaccine types
where we've modified them,
but we're injecting that presentation,
that purification,
no RNA component involved in those critters.
Now, when we're coming to,
so this one, actually, I won't come to that yet
because that's the COVAX,
that's a bit different.
So now when we come to the viral vector vaccines,
this is a bit tricky.
So what we've done is we've taken a virus,
modified the virus.
So we do this through all sorts of ways,
but they've made it that the virus
is supposedly what they call non-replicating.
So that the virus is unvirus.
shouldn't be able to, although they now say up to 10%
grow in our bodies, that we take a virus
and the common ones that they used is an adenovirus,
which are usually relatively benign.
The AstraZeneca is a chimpanzee adenovirus.
So they take an adenovirus, they alter it
by taking out some of its DNA,
but then they plonk in what they want,
the gene that they want plonked into it.
And so this is where we get recombinant technology
and that then gets injected in.
So these types, and then again, the DNA vaccine.
So that is injecting a little bit of genetic material
in the viral vector one,
that is injecting some genetic material.
The DNA vaccines are injecting genes and genetic material,
but those are all getting injected basically
into the cytoplasm, into the main part of the cell.
And so this is where we activate the sort of processes
I spoke about before.
Here's your dendritic antigen presenting cells
that kind of gobbles this up,
presents it to your T helper cells that gets on the game
and says, okay, guys, we've got a problem here,
activate everything.
So the B cells then start making antibodies.
Here's the virus coming in.
The B cells make antibodies to try and cloak the virus.
The T cells are getting going
and some doing some killing themselves
to destroy the infected cells.
But all of this,
so see, we've done nothing with mucosal immunity.
This virus has been injected directly into our system.
So the whole first level of protection
has bypassed completely.
So it's directly injected into the system,
which is not how we get the virus, natural COVID.
We breathe it.
So the whole first arm of the immune system is negated.
So what about somewhat more nasty vaccines?
So let's come down to the mRNA antigen presenting.
Here's our mRNA vaccine.
What's that?
This is it.
Am I meant to be hearing any of that?
No, yes, no.
Okay, here's our mRNA vaccine.
Now, what this actually isn't showing in here,
it is just showing it get injected in,
but what they're not actually showing is that,
and I'll come to this more actually,
because I've got a particular slide
just on the mRNA vaccine.
But the point of this one really is to show you
that you've got all these different types of vaccines.
So let's skip on through.
So in Australia, we've so far
really only got these three types.
We've got the AstraZeneca, which is a DNA vaccine
carried on an adenoviral vector, right?
And it's got the gene for the spike protein.
I'll be talking more.
We spoke last time about what they've done with that gene.
The so-called genes that they're using
for the spike protein in the vaccines
are not exactly the same as the genetic profile
of the spike protein in the virus.
They've modified it to make it, let's say, stick more.
Your Pfizer, this has got your lipid nanoparticles,
synthetic lipid nanoparticles,
which we have now, which has been proven are toxic.
They accumulate, particularly in the ovaries,
everywhere in the spleen, in the brain.
And they encapsulate your mRNA
that encodes for these altered spike proteins.
Then the Novavax.
So I'm gonna talk a little more on that.
We have already touched on it.
Novavax is being touted as your safe alternative.
However, it is synthetic.
It is still a nanoparticle.
What do we mean by nanoparticle?
So small it invades all the normal body systems.
It will get into brain tissue.
And it's coated with spike protein, trimer, trimeric.
I will talk later, maybe not today,
about the three components of your trimeric spike protein.
Matrix M, this is a saponin,
so irritant from a plant as an immune-boosting adjuvant.
That what they're saying
and trying to put in nice language there
is that matrix M irritates the immune system.
So the body puts a stronger immune response
because it's not nice stuff.
So there's our vaccine types.
We're gonna whiz through that now
until I get to the diagrams,
because we spoke about that
and that's in your slides from last week.
So here's your picture more on how these viral vector vaccines work
and how they actually are inducing immunity, so they say.
So here's your SARS-CoV-2 up here.
They stick it into a virus.
A replicating virus would be if they used a weakened measles virus,
which they're not for.
A non-replicating virus is the adenovirus.
So they inject that in.
What's supposed to happen then is that that then creates the spike proteins.
It basically creates your SARS-CoV-2 but without its infectivity,
but let's say creates the spike proteins.
The dendritic cell comes along and goes, uh-oh, okay, we've got this problem,
and then it goes to the T cells and says, get us some help.
The B cells make the antibodies and the T cells do some destruction.
So we do get some activation because it's coming from the cell
and then getting expressed out ourselves.
You see, that's the point with all of these DNA and RNA things
is that by them cleverly finding a way to get it into our cells
and then getting expressed back out of our cells,
because our cells have got a process in making it, right,
our antigen-presenting cells will go, uh-oh, these cells have been infected
with something, and they will get the T cells going as well as the B cells,
but still not mucosal immunity.
So that's your viral vector cells.
Here's your DNA vaccines.
Now, in Australia, our AstraZeneca combines the DNA component
with your viral vector.
So, again, in your DNA vaccines, the spike gene is directly put in a way
that goes right into our DNA, our DNA, our incorruptible seed that God made,
the blueprint of life.
The AstraZeneca and the DNA vaccines put spike protein genes directly
into our DNA.
That then makes the messenger RNA.
Our DNA then gets encoded.
That message in the DNA gets read to make the messenger RNA,
so we then make spike protein that comes out for the antigen-presenting
cell to find and trigger the immune response with the T cells
and the B cells.
We are making it.
But in the DNA ones, the AstraZeneca, we are making it via our DNA
being altered, irrefutable.
The RNA vaccines, they send in some messenger RNA that goes to our –
so the messenger RNA, what the step they're not putting in
in the middle there, goes to things called ribosomes,
and they read the messenger RNA and make the protein.
So the viral proteins are made.
Now, the issue with the messenger RNA is that there is another enzyme
between our ribosomes, between our messenger RNA and the DNA.
So the DNA makes the messenger RNA via an enzyme called transcriptase.
It reads it, it transcripts it, transcribes it from the DNA to the RNA.
But there is also an enzyme called reverse transcriptase that takes
RNA message and reads it back into DNA.
Now, they used to think, like so many things, we think we're so clever,
they used to think that we didn't have reverse transcriptase
in human cells.
But they've come to realise, recent studies, we do.
Not a lot of it, but we do.
So there is most definitely the potential for at least some
of that messenger RNA in some people to be reverse transcriptased
and read backwards back into our DNA.
Again, incorruptible seed being corrupted.
So that's how the DNA and the RNA vaccines work.
So looking at that a little bit more.
So they're trying, this is from the manufacturers,
so they're trying to make it look lovely for you.
So we take the spike protein, we make the mRNA, we make a vaccine,
we get that into the cell.
The cell then makes the spike proteins.
The spike proteins then get transferred to the RNA.
trigger the body to make antibodies
and those antibodies go and coat
cells that are infected with COVID.
So that part of it is basically correct.
The question, as I said,
this whole question that we've just been through
of how the cells are making the spike protein
and what the implications are of that is the problem.
The other issue is, whereas with the original vaccines,
there's a limited amount of spike protein injected.
What we don't know with this system
that is putting the vaccines into the cells,
what we don't know is for each individual person,
how much of this spike protein is produced
because it varies between people.
It varies for a whole heap of factors.
There are some studies that indicate
there can be a billion fold more being produced
because when you think about it,
this technology is able to get into all our cells.
And they know this from the lipid studies.
So they studied the biodiversity,
the biodistribution, sorry, of the lipid nanoparticles
and they're going throughout the body.
So cells throughout the body are being activated
to make spike protein to create the antibodies.
So that's your mRNA vaccine.
So I wanted to, whoops, just put up for you last time,
this picture of Gabby.
So this is your global vaccine alliance.
And so who's in this?
The vaccine industry.
Vaccine industry, some civil society things,
independent individuals.
Well, that's interesting.
It'd be nice to get a full list
of our big independent individuals
because there's only nine of them.
Bill and Melinda Gates, governments of donor countries,
World Bank, UNICEF, World Health Organization,
the governments of the implementing countries.
Doing that five and five, yeah.
So you can see it's an interesting group.
And these are the ones who are creating the vaccines
and telling us what vaccines we should be using.
And this was just the picture about the different vaccines.
We went through all these different vaccines last time
and you can at your leisure go back through them again.
But where I will come up to is the question of,
so what's happened to my COVAX picture?
No, that's not the one I want.
Okay, we've already spoken about the Novavax.
So yes, here we go.
So COVAX, Novavax.
So this is, I said, is the one that is being touted as being,
this is our safer alternative, they're telling everyone.
So here's what the COVAX is doing
is that it's coming in here
and they're saying that it's breaking the cleavage site
that enables your SARS-CoV-2 to get into the cells.
So that's where they're saying the COVAX is working.
Cut down the administration problems.
So they're saying it's got fewer side effects.
I spoke about the development of the CEPI vaccines,
COVAX, your Pfizer shareholder.
So I'm gonna finish,
we're gonna come back to this next week,
but I'm gonna finish this slide on this particular slide
and this particular part of the presentation
on this beautiful graph.
For those who say that these vaccines are safe.
So this is taken straight
from the vaccine adverse events reporting schedule
from 1988 when it was first started to 2021.
The COVID-19 vaccines, of course,
have only been in for a short time,
but look at the massive number of side effects
that have been produced in that short space of time
by the small group of vaccines
compared to all the vaccines that have been used globally
that we've got side effects recorded for since 1988.
You really don't need to say anything, do you?
This speaks for itself.
These are the most deadly vaccines
that have ever been kept on the market without a doubt.
Without any doubt.
So you have to then be asking, why is that?
Why are these vaccines not just still on the market,
but why are they actively being pushed?
When the facts are,
this is from their own adverse reaction database.
And we know.
from other studies that have been done,
that this adverse reaction database,
because it's totally voluntary,
is only picking up between one and 10%
of the actual reaction rate.
So we know the actual reaction rate is way higher,
perhaps 100 times higher.
That speaks for itself.
So that shows you just how dangerous
these vaccines really are.
So any of your friends who think there's nothing to it,
say, can I show you this one picture?
This is from the USA Vaccine Adverse Reaction Schedule.
Can I show you this one picture?
So that's that.
So again, I'll flip out of this and stop screen share
and just come back to you guys for a minute.
Are you all still here?
Yeah, you're kind of all still here.
Yes.
Haven't knocked you off.
So yeah, Robin, that's exactly right.
This is all of what I'm talking about
with everything I do is about how to keep
that mucosal immune system healthy,
because that is our absolute key thing.
Your gut lining, your respiratory tract,
we have to keep our human,
our mucosal system really good,
but God's got it all under control.
So that's talking about the vaccines and the vaccine types.
And as you read through that,
I've spoken about what they admit to being in the vaccines,
but there is another big thing that they are not
at this point admitting to being in the vaccines.
And with the research that I've done just recently,
I'm somewhat concerned that this may be an even bigger issue.
So I'm just going to close this one down
and open the one that I want,
assuming I can do that with you guys still being there.
So just hang with me for a second while I pick it up.
So I did some rabbit holing on this
because I felt the Lord saying
I had to look more closely at this.
I hadn't looked at it overly closely before
because I was waiting for more data.
I was aware of it,
but I was waiting for some more data to come in.
So the data has now come in enough
for me to speak out on this.
So here we go.
So what I'm going to talk on now is graphene oxide.
So probably a lot of you have heard
about the graphene oxide.
So I'll talk through the chemistry of it first.
So the thing about graphene oxide, it's unique.
It's a unique substance.
So we know it historically as graphite.
So lead pencils got replaced with graphite pencils
because we were killing ourselves by chewing lead pencils.
So they replaced it with graphite, which is sheets.
Graphite is sheets together.
So graphene is a single sheet.
This is unique in nature
because it's two-dimensional only.
Two-dimensional, flat, total flat.
There is no depth to this whatsoever.
It's one molecule depth, one atom depth only.
Not a molecule, one atom depth only.
All of this structure that you see there,
let me get my thing.
All of this structure that you see there is carbon.
Those are all carbon atoms.
Carbon, carbon, carbon, carbon, carbon.
They're all carbon atoms.
One atom thick.
So they can alter the size of it this way
and that way and every other way.
They can make it into,
and I'll come into the piggies
of what they can make it into,
but it's carbon.
It's flat.
We meant to be seeing something again on the screen.
No?
What's that?
We meant to be seeing the picture on the screen again.
No?
I've hit share screen.
Haven't you got it?
No, not yet.
Oh.
Sorry about that.
Okay, thank you for telling me.
Well, let me hit it again.
I'll escape from this
because it doesn't let me do it if I've not escaped.
So let me see if it'll let me.
No, it's not letting me escape.
Share.
Let's try that again.
This is working.
Yeah.
Now it's working.
Okay.
Here's the graphene oxide.
Sorry, guys.
I'm learning fast about technology here.
Here's your graphene oxide.
So these are all carbon atoms.
Nice big honeycomb.
Nice structure.
But that's single atom only thick.
Single atom only.
So effectively it's a flat.
two-dimensional structure, unique, flat two-dimensional structure with a whole heap of sharp edges.
So they can make it bigger, they can make it smaller, but it's pure carbon, flat.
And it is now being widely, hugely, hugely, hugely used throughout industry.
One of the features of this thing, highly electrically conductive, highly, highly, highly.
We'll come back to the relevance of that for humans in a little bit.
Extremely conductive, it's water, well not water-soluble, that's not the right thing.
It's not water-soluble, but it likes to attach to water.
And super strong, super strong, it's thought to be the strongest substance out.
Can be made into a whole heap of things. So here are some of the...
Why does it not want to do that? What happens if I do that?
Right, so here are some of the things that can be made into...
So graphite is where we have it in plates, that can be made small, and that's micro, small.
Graphite plates, micro oxide, but then we come to graphene oxide.
Graphene is where it's a single plate, so they call it micro when it's a certain...
So here are your measurements here.
So micro is not too small, we used to think micro was very small.
Nano plates are smaller still.
So tiny, tiny, we're coming down to less than cellular level.
Nano graphene oxide, and this is a critter we're talking about.
Nano graphene oxide, single layer, very tiny.
Not a natural substance.
So here are some of the shapes and sizes they can put it into.
So this can be made into tubules, it can be made into building blocks.
But this gives a bit of a... starts to give you a graphical representation
of what these plates, they're razor sharp, flat, flat, molecule-only thick plates.
They can literally cut through, and they do, literally cut through our cell membranes,
literally cut into and insert themselves in our cell membranes,
literally insert themselves here, they are here, some in here, some in here,
they just get anywhere.
Graphene nano oxide or nano graphene oxide.
As I said, being widely used now in all industries, widely, widely used.
So how is it getting into our cells?
Nano graphene oxide.
Tiny enough molecules, these ones, this is where it's down just to the two
little bits of the molecule, just straight in.
Nothing stopping it, straight in.
Breaks down to the single carbon structure, porphyrin ring,
that's what we call porphyrin ring, straight into DNA,
straight into the nucleus, not a problem.
Causes DNA damage directly.
Or it gets engulfed.
What the cell has a process called endocytosis,
where the cell membrane will go around something,
and so it gets engulfed.
The body tries to break it down, breaks down a little bit,
but that causes more of a problem,
triggers an inflammatory response,
and this is where we get to those cytokines,
those interleukins, things that I was talking about before.
Triggers an inflammatory response.
Triggers the release of calcium.
Calcium being released intracellularly kills cells.
So that causes a release, the damage to this,
the endoplasmic reticulum causes release of calcium.
How else is it getting in?
It literally, as you saw on the other diagram,
cuts the cell membranes,
sheets it, literally cuts the cell membranes.
Once again, the body can break it down a little bit
when it comes in, but it triggers all these processes.
The other big thing it triggers, ROSC, it's all looking angry.
That's reactive oxygen species.
Basically fire, cell fire.
That again damages your endoplasmic reticulum.
You get calcium being released, which causes cells to die.
Damage to the DNA, damage.
This is our mitochondria over here.
This is all happening inside the cell.
This is our mitochondria over here,
and the mitochondria is where we make our cell energy.
gene. This is our little cell powerhouse. This is getting damaged by these reactive oxygen species,
we get calcium release, they die, the mitochondria die. What else is it doing?
So this is where it just pushes its way in, basically, or the phagocytes eat it. So that's
a phagosome there. So the phagocytes, remember those, those dendritic, those phagocytic, those
Pac-Man cells I showed before, they try to eat it. So the body is trying to protect against
this stuff. But the bottom line is it can't. Nothing that we will normally do in our system
is working against this stuff. So breaks it down, but that just triggers inflammation,
release of calcium, reactive oxygen species, damage everywhere. So that's how it's getting
into the cells. So this is just showing again, some of the systems that are activated.
Don't worry about any of those letters, you know, you're never going to hear them again.
But here's the sheets of your graphene oxide, graphene oxide in its sheets, it interacts with
these, it's in these ones, it's interacting with these, these two particular types of receptors.
That's one called tumor necrosis factor that activates a whole heap of nasty pathways
that lead to caspase 3 leads to cell death. Apoptosis basically means it's kind of like
the cells explode. So cell death. This one activates this other receptor called TGF3,
transformational growth factor 3, triggers off another whole heap of cascades, the JNK cascade,
which causes nuclear damage, comes into the nucleus, comes down to the mitochondria again,
causes damage, we've got really activation of this critter causes more inflammation.
Over here, this TNF alpha tumor necrosis factor alpha comes down and causes the cells to die.
So basically, this whole message is inflammation, death, death, death by various routes
in the cell caused by graphene oxide in nanoparticular form. What else is it doing?
Here's our graphene oxide again, coming in on different receptors. So we've said a few
different ways it's getting in already. And here's some more ways it's getting in.
Toll-like receptor 4, toll-like receptor 9, activates another set of pathways,
more reactive oxygen species. That's also oxidative damage, reactive oxygen species,
oxidative damage, DNA damage. So the mitochondria, sorry, the DNA then is making messenger RNA
that's sending out help messages to everywhere, cytokines are help messages, but that's creating
more inflammation that's causing cells to die. Because the body is basically getting the message
my cells are corrupted, better kill them. So the cells die. Toll-like receptor 9 again,
autophagy, this is a phenomenal response the body has where it basically eats itself.
So the cell flips on, it says this cell is dangerous, it's dangerously infected with
goodness knows what, don't know what this stuff is, but I don't know what else to deal with it,
I'll kill myself. So autophagy, the cell eats itself. So phenomenal stuff that is happening
in the face of this graphene oxide. So the last, well, probably not the last really,
I think we literally only just begun investigating what, it's the old story,
science is streets ahead of the biology. So the science field and the industrial field has been
playing with graphene oxide for quite a while. You'd be surprised all the places it is.
But the biology is just beginning to catch up with what the heck happens if we put this in us.
So this just shows a whole heap of places where we're seeing what goes on with the graphene
oxide. So let's start at the top here. The graphene oxide is interacting with our blood
vessels and our blood cells and causing clotting. It's interrupting the normal process of blood cell
breakdown when blood cells, because there's a normal cycle where blood cells will break down,
it's interrupting that. It is activating what we call complement, and the complement is another
pathway in our body that gets activated when there's something foreign. Clotting is a mechanism
that our body deliberately will activate when it says there's something I've got to wall off or
stop. So of course, the obvious thing is if a blood vessel is cut, the body says, I've got
to wall this off so you don't bleed to death. So it activates the clotting.
cascade. So what the body's done here is that these are nanoparticles activating the clotting
cascade. So the body just says, well, there's something going on in my blood, I don't understand
don't know quite what it is, it's activating these pathways, let's just seal it all off.
So it clots it. The macrophages are trying to eat it. Can't do anything with it when
they do eat it, but they're trying to eat it. These are our androgenic, our dendritic
cells, macrophages. So here's our other macrophage. And then we've got this, then this activates
our B cells. So then we're getting an abnormal B cell activation. Because again, it's kind
of trying to do something, but it doesn't know what to do. And here's our lymphocyte,
that's a red blood cell, here's some lymphocytes being affected. So it's doing all of these
nasty things, cytokines, it's getting release of these cell messengers going around, all around
the system. Now, the other interesting thing that they're learning about, see, these are our
proteins in our plasma, we've got all these proteins that float around in our blood.
What's happening is the graphene oxide is connecting to all these proteins,
it's sticking to it, it's attracted to them. It's connecting with all these proteins and causing
what they call coronas, graphene oxide coronas. So it's like the graphene oxide stuck on the
outside of them a bit like a crown. So we're back hearing about corona, coronavirus,
isn't that interesting, coronavirus, and we've now got graphene oxide coronas.
So it's all sitting on the outside of the proteins. And again, activating all these
things, it's going around and activating all this stuff in our bloodstream.
You can only, you know, hard for us to conceive what the effects are or are going to be of all of
this. This is just a straight print from a paper, straight screenshot from a paper listing
all the proteins that graphene oxide will link to.
And it's a horrendous list. So here's a complement component, that's clotting.
Prothrombin, that's clotting. Alpha-fetoprotein, that's related to cancer. Fibrinogen, that's
clotting. Vitamin D binding protein. Vitamin D, the calcium, the graphite is binding to our
vitamin D binding protein. The cytochromes, cytochromes are involved in energy production.
Lipoproteins, this is transport of your fats, so we can't get fats where they need to go.
It's binding to transport proteins, it's binding to immune response proteins,
so it interrupts with our immune response.
Alpha-trypsin inhibitor. So this is interesting. Alpha-trypsin is a degradating enzyme that we're
supposed to be able to shut down, it'll cause too much problems. And this is binding to that,
it's stopping it shutting down. Goodness knows what that's going to do.
And then a whole heap of these other things here. Reduced protein binding.
On we go. IgG, immunoglobulins are getting bound to the graphene oxide.
So there's other things that the... So the one, the particular one that it seems that we have,
that we are dealing with is graphene oxide pig.
They call that pig-elated. PEG, polyethylene glycol. So the pig-elated
graphene oxide seems to be the form that they're using of concern for us humans.
So graphene oxide. So what are they doing with this stuff?
So as I said, aside from being widely used in industry,
graphene oxide is being used as a nanofiller. So this is just by the by. Very effective,
very cheap to make. Graphene oxide is incredibly cheap for them to make. So they're looking for
all the places that they can put it to replace other things. Guess where some of the places are
that they're using graphene oxide as a nanofiller? COVID face masks.
Numerous of them, numerous types now of the masks used for, that we are told that we must wear,
have been found to contain graphene oxide as a nanofiller.
But antigen testing, your nasal swabs,
your antigen testing, again, it's been proven.
So this graphene oxide is being used in industry
all over the place.
So here's where they're talking about
using graphene oxide in a nasal vaccine.
They're very taken with graphene oxide.
So here's your graphene oxide.
They bind it to what they want to bind it to.
And so now they've got graphene oxide.
In this case, they're using a polyethylene instead of a pig.
And now they've stuck on the stuff they want.
So here's your graphene oxide
with the antigen and the adjuvant.
Adjuvant, you know, they always use nice terms.
Adjuvant is to stimulate the immune system.
Adjuvant is an added immune irritant.
The immune system doesn't like adjuvants.
That's why it reacts to it.
Anything the immune system is reacting to,
it's reacting to because it thinks it's a problem.
It's a problem.
So along comes our graphene oxide,
antigen, immune adjuvant.
The dendritic cells get a hold of it.
They make some cytokines, some cell messengers to come in.
This comes into our mucosal membranes.
This is the only good thing, if you like,
that I can say about this vaccine
is that it is actually coming in via our mucosal system.
The bad thing is it's graphene oxide
coming in via our mucosal system.
So it comes in through here and now they forget about.
So you'll notice after this,
because this is an industry slide.
So it's all about how good it is.
There's no, where's the graphene oxide gone?
Funny that it's magically disappeared.
So there's no talk here about how the graphene oxide
is doing anything.
This now only is because, well,
we've just got an immune adjuvant
and we have managed to activate T cells
and activated our B cells.
So they've made our secretory IgA.
Yeah, that's good.
They've made our IgG that goes through the whole body.
So yes, it was found to significantly boost
and cross-react immunity.
Yeah, that would be true.
It would have done that.
So that when they then later challenged,
this was a mouse study,
when they then later challenged the mouse with a virus,
it worked.
Yep.
Because it's coming via the nose,
but the big problem, it's a graphene oxide-based system.
Graphene oxide in vaccines.
Here's a study from 2016.
So they started playing with it a little while ago
and they said, hey, look, you know,
they were starting to recognize
that the problem with the other vaccines
was that they weren't getting cellular immunity.
Okay.
So let's just quickly read this.
So you get a benefiting
from their unique physicochemical properties.
Graphene oxide is unique.
And so they've attracted great attention in biomedicine.
Industry likes it.
They're cheap.
They do incredible things.
They're highly electrically conductive.
Fantastic.
So they engineer them as a vaccine adjuvant.
What?
What's that?
As a vaccine adjuvant.
But what do we just say about adjuvants?
Adjuvants irritate the immune system.
So they used it for immunotherapy.
So attached to polyethylene glycol
and polyethylene imine to coat it.
So, da, da, da, da, da.
And so what does it do?
A positive modulator to promote maturation.
In other words, it irritates the dendritic cells
and makes them wake up.
Makes them secrete their things,
their cytokine secretion.
Remember I spoke earlier about the toll-like receptors.
So it's activating all these
and it says activation of multiple toll-like receptors.
In other words, lots of arms of the cell,
parts of the cell membrane go, uh-oh, here's trouble.
Multiple toll-like receptors.
Now they say it's showing low toxicity.
They're only talking about acute toxicity.
They're not talking about what happens
if we've got graphene oxide coming all over the place.
And so that graphene oxide PEI
becomes a way to shuttle antigens into the cells.
Well, no surprises on that.
We've just shown how this graphene oxide
is sheets that cut into things.
So of course it can get where you want it to go.
So it is a novel vaccine adjuvant.
And so they checked that out and said, yeah, this.
works well. It's novel, and it's highly effective. We like that. So research kept going.
2020 now. And so he was asked not to make the point that the development of new vaccines,
such as our nucleic acid vaccine, so RNA and RNA vaccines, and hang on,
synthetic peptide vaccines. Oh dear. What was that one? Novavax. Synthetic peptide vaccines
have achieved rapid development. However, compared with traditional inactivated or
live vaccines, they often have problems such as poor immunogenicity. In other words,
we've made these great new vaccines. They're not irritating the immune system enough. What
else can we do to make them irritate the immune system so we get antibodies form?
We need an adjuvant. There are many types of adjuvants,
the most commonly used, so aluminium. I spoke about that last time.
But a new generation of vaccines will probably need new generation adjuvants.
June 2020, recent progress of graphene oxide as a potential vaccine carrier and adjuvant.
We can skip through all of that, but basically urgent need to develop new
all-purpose adjuvants because some of the adjuvants approved for human use have limited
functionality. Graphene oxide, widely employed for the delivery of biomolecules, excels in
loading and delivering antigen and the potential of activating the immune system. Now they say,
hang on, bit of a problem. Graphene oxide aggregates in biological liquid induces cell
death. So you have to find another way to do that because we don't want the cells to die.
So we come to this, here's our statement. So what's our summary? Our work describes the surface
modification of graphene oxide and for the first time summarise that functionalised graphene oxide,
so we're still using graphene oxide, but we've pegged it, serves as a vaccine carrier and shows
significant irritant. Whenever you see adjuvant, replace it with irritant activity in activating
cellular and humoral immunity. The cellular, this is your T cells, your macrophages, humoral, this
is your antibodies. In the future, it is expected to be introduced into vaccine research to improve
the efficacy of vaccines. That was June 2020. There has been a patent put out for graphene
oxide in vaccines as a vaccine carrier. Now, unfortunately I couldn't find that again. I
cited that some time ago. So I suspect it was 2020 that that patent, I had in my head it was 19,
but it might've been 2020 that that patent was put out. So it is patented for use. It is being used
now. And here it is in a Raman spectroscopy of the Moderna vaccines. So I was holding off
saying this until I, you know, I was basically saying, Lord, I need a bit more behind me to talk
on this. So we've got two separate units now. The first unit to talk on graphene oxide in the
vaccines was La Quinta Columna University, Italy. And they did that 2020. They were first
cab off the rank. And they wrote, you know, they made a video at the time. They did a press release.
They wrote a paper and they basically said, we're finding this in all these vaccines. We're deeply
concerned, but not really anything else happened. This is a new spectroscopy from a UK lab. So a UK
lab has replicated the work and done all different types of testing, but including, I put just this
one up because this actually shows it to you, all the others are measurements that, that, you know,
without that don't mean a lot to those who aren't trained in it. So I put this up to literally show
you. So here it is in the Moderna vaccine. They've also seen it in they've seen it in all the mRNA
and the DNA vaccines. Unfortunately, in that one, they didn't test the Novavax. So I can't
categorically say it is in the Novavax. And I won't say it is because I haven't got proof.
But I suspect it is because it is made in the CEPI. It's under the CEPI umbrella. It's made by
this in the same group of as these vaccines, the other vaccines that contain it. So I suspect it
has, but I cannot prove it. So what's the problem with these things? Remember I said
that so clearly this is not separate when you look at this this is clearly not separate
nanomolecules is it it's aggregated it's it's come together and and this is the deep concern
that we have with the graphene oxide which is because it is so highly charged and there
are actually some videos that show this because it is so highly charged it it's almost like it
comes alive under the influence of electromagnetic radiation and it aggregates it's like it grows
it can't grow there's a limited number of in there but it joins back to our body works hard
to separate it it joins back together under the influence of electromagnetic radiation
and so it's pretty obvious to see why something like that in our system is going to be an easy
focus then for for clotting and other problems so personally i now believe that um
stop screen sharing now
so i now believe that the having really looked into the data on all of that now and read a lot
read a lot of a lot of paper writing to pull to pull all those together reading to pull those
together i personally now believe that the graphene oxide is at at least um
at least as much an issue in the vaccines as a spike protein my suspicion is it's actually
more of an issue than the spike protein so um it's a huge question so coming through
coming through some of these questions sort of relating to this so is this why some people think
their skin is magnetic well if the graphene oxide has pulled together at that point yes
graphene oxide could be magnetic it is highly charged it is highly conductible that's the
whole point about it that's why they love it in industry they love it in industry it's being used
everywhere so so the pcr test every three days to yeah well that's right so so this is where we
can you start the more you dig and the more you look around all of these things you start seeing
all these very very suspicious correlations do we have proof of every individual part well i'm very
careful to not actually lecture from pulpit on something that's recorded for something i don't
have some kind of proof for so um i can certainly say that and i've picked this up by looking at
there's a particular company nano graphy that is quite happy to say that its uh antigen testing do
contain nanoparticles so so we know and and we know for a fact i think it was in canada that some of
the masks were withdrawn because graphene oxide was proven in them so those are facts so we can
certainly say that graphene oxide was in must we can certainly say that graphene oxide has been
proven in some of your testing kits and and no doubt you know some of your swabs can we say that
it's in all of them of course we can't um we can surmise that it may be we can surmise that those
who are behind everything who said this is what we must do might even have known this science they
might even have known that graphene oxide inhaled into the lungs is very dangerous stuff possibly
we can't prove any of that so so the reason they're putting the graphene oxide in is that
they're discovering two things it's a great carrier right they can stick the stuff to it and
it carries into the cells it cuts its way in it gets sucked its way in it does all it interacts
with all the receptors all these multiple ways that this graphene oxide will get into the cells
multiple ways so graphene oxide that's our first thing it's a carrier what's our second thing
a very powerful immune adjuvant very powerful immune irritant very powerful immune
stimulator so the graphene oxide is serving two purposes
all right so so very very much a problem um it has to do the whole thing about the
graphene or the other big thing around graphene oxide is its charge it is extremely strongly
negatively charged and here is a big problem for us because when we are healthy we're negatively
charged the flow of electrons throughout our body that creates energy is negative
okay so when we're healthy we are negative
negatively charged. So this creates another whole section of issues with when I start
talking later about, well, how are we going to detox this? Because all our routine detox
mechanisms that we've used, nutritional things like this that we've used for a long time
and centuries and all the rest of it are positively charged, because we're used to dealing with,
sorry, are negatively charged, because we're used to dealing with positively charged toxins.
we've had to deal with before now are positively charged. This one isn't, it's negative, strongly,
strongly negative. So it's, it's very, it's quite unique. It's very strange.
So, so yeah, binding to the vitamin D protein.
We do not know. We simply do not know. These are so these are all effects that have been shown in
animals, in, you know, test tubes in biochemical labs and so on and so on and so on. So we know
that it binds to all these things. Do we know what effect this is going to have in the human body?
Of course we don't. It has not been tested and nor would it be tested.
So not only have we got experimental mRNA DNA vaccines, but we've got experimental
and human vaccine delivery systems, which independently have been shown to have the
potential for extreme toxicity. You know, extreme toxicity.
Jumping across, I'm going to jump into a bit of a strange hat here for a minute.
In, in one of, I'm part of Global Ascension Network, and part of what we do is, is ascend
into the heavens, see what God is doing and decree and declare and bring that back down.
One of those sessions, fairly early in the vaccine piece, we felt the Lord was showing a giant
waterfall. This was the river of life that had come from out from under the throne room and then
had cascaded into the waterfall. And we were told, God told us to bring all our friends and the people
we knew who'd been vaccinated and put them into the waterfall. This was after we'd been in it and
we were shining light and everything was gorgeous. We had to bring these people in. And what I saw,
because I'm the main seer in that particular group, what I saw was that as the waterfall
washed through, coming out the feet of these people was thick, black, like squid ink.
It was incredible. I sensed it was pure evil. But at that time, I hadn't put two and two together.
At that time, I hadn't done enough reading on the graphene oxide. Because what they are seeing in
the pathology labs, when they look at things and look on a histopathology level, the places where
the graphene in the animals, the places where the graphene oxide accumulates is black.
It's turning tissues black where it accumulates.
So for all those who think along those kind of lines,
get your water pictures, get whatever anointed, anoint the water, claim it, start pouring it on
people. We've got to we've got to wash claim because truly none of none of our standard
detox things and I've been working in this field for 35 years can work against graphene oxide
because of this charge component, it's got we've got to do it differently. Since Washington plane,
Washington plane in the water of the word Washington plane from the river of life that
is coming directly from the throne room. So it's a yes, incredible stuff. So graphene oxide, as a
non admitted ingredient in their vaccines, and yet all the evidence is there from the literature,
from the studies that have been done on the vials. And increasing studies have been done
the New Zealand group now, your wonderful New Zealand doctors, I take my hat off to you guys,
you are streets ahead of us here in Australia. I've got a pat more on it. Yeah, just congratulate
them. Your wonderful New Zealand guys are mounting a court case at this point of time. And part of
what they have done is have had the miles independently assessed. So I might have a
little chat to my friend, Matthew Shelton and just see what they found. So, so yes, so that's
that's that. So we've got another 20 minutes, I could talk into 30 other component of this,
because I want to leave the full thing of sort of talking around the vaccine side effects and how
are we going to treat that form, we've got some people in next week. So I know we've got at least
one, I think I've got two organized, I think.
I'd like everyone now that, again, now that you've heard this, okay, now that you've heard this, please, everyone go out and talk to some of your friends who have been vaccinated and say, hey guys, would you like to, you know, have you got, would you like to tell your story of how you feel and what's happened with that?
Would you like to hear some ways we can perhaps help you get better again?
We really do need to, we've got to pull people back from this stuff.
So the spike protein, so back to the spike protein, I actually didn't get to pull the slides and the pictures back to this.
But I did comment, you heard me talk on the way through how the spike protein was a trimer.
Heard me say that word?
Trimeric, tri, right, three in one.
So the spike protein is trimeric.
People have called it a trimeric chimera.
What does that mean?
Three parts to it, chimera, this is your, a bit like from chameleon, but it's been put together.
So three separate parts that have been put together.
So the original spike protein has been intensely modified.
So your spike protein, so as we're going back to the original of your coronavirus, so your original coronavirus was like a bat cold, okay?
Everyone's happy with that?
So the original coronavirus was basically a bat cold.
And they played with it in the US labs.
Again, there's documentation to prove this.
There are published papers to prove this.
And they were doing what they call gain-of-function research.
And they played with this spike protein.
And the first thing that they did was to play with the ACE and insert an ACE receptor, angiotensin enzyme receptor.
And this was going to attach it to most of the human cells, because most of our human cells have got an ACE receptor, particularly in our blood vessels, particularly in our respiratory tract.
So that was going to get it in.
So they played with the ACE receptor.
But then, you know, the research got mucked up in the US and ostensibly shut down.
So instead it got slithered underground and made its way across to China, to the Wuhan lab.
And there are only a number of the Level 5 biosecurity labs around the world.
And Wuhan happens to be one of those.
So the highest biosecurity labs you can get in the world.
So it made it into the Wuhan lab.
And again, published papers by the scientists there, happily boasting about their gain-of-function research.
And that can be tracked down and proven.
So further gain-of-function research done.
So if we look closely at this spike protein, we see that there are another two things that have been inserted into it.
So yes, it's got the ACE receptor protein, so it can attach to human cells.
But the next thing they put in was a furin cleavage site.
So furin is a particular sugars that we have, fucose, but particular sugars we have in our cell membrane.
So the furin cleavage site meant that they put into this spike protein the ability to attach to these parts of our cell membranes and break it open.
So not only is it attached to the ACE receptor, but now it's got a way to break the membrane open.
So it breaks the membrane open, and then the rest of everything pops in.
So that's two parts of the three.
What's the third part?
The third part is that it has a particular DNA sequence that happens to be homologous, happens to be the same as, surprise, surprise, HIV.
Now obviously they're not injecting the whole HIV virus, they're not.
But they're injecting part of the DNA, part of the spike protein is homologous with what comes with your HIV virus.
So we've got, it attaches to the human receptors, the ACE receptors.
It is able to split the membranes open, but now it's putting into our cells some of the genetic code from another probable synthetic virus or altered virus, let's say.
Altered virus, because it started off as a simian immunodeficiency virus and then courtesy of polio vaccines jumped into Africa.
So affects the immune system.
So that is coming in with the spike protein.
So that's the coronavirus spike protein.
But then what they've done with the vaccines, they've gone a bit further than that.
So we've already got spike protein we're putting in with ACE receptors, it can attach to our ACE receptors, it can still do all of that.
The spike protein that we're putting in can still bust open our cells.
We've still got the HIV component, but there are a couple of other things that have been done to it.
done, and I touched on this through the lecture, is that they have replaced particular of the amino
acids in the sequence, and put in some proline. And that doesn't sound like anything particular
anywhere. But proline is one of the main amino acids in our connective tissue. So what is it
about our connective tissue, the connective tissue cross links, connective tissue sticks with itself,
that's how it's strong. So it's got cross linking. So they're stuck proline in the spike protein,
so it will be sticky, it's going to cross link, it's going to be harder for us to break it down
and clear it. Next thing they've done, this one is, and that one they admit, this one they haven't
admitted, but this has come out from the work of another research scientist and Dr. Stephanie Seneff
from MIT USA. And what she's found is that they have also put in more guanine, guanidine residues,
so G. What that means is that the folding of the protein of the spike protein is different.
Proteins and DNA all expresses according to how much it's folded. So the folding is different.
And as a result of this difference, it appears to cause, and I'll talk more on this next week when
I'm talking on the side effects of the vaccine, but the folding is different. So the effects in
the body are different. So there's all these things that they have done with all of this.
So it's not just the spike protein itself that they engineered, which is altered from the original
virus. And interestingly, as the virus mutates, it looks like it's losing some of these things that
we humans stuck on it. That's rather nice if in fact, God, you know, that that's what's happening.
God is winning. It's going back to what he first made. And doesn't that make sense? You know,
because what God made is infinitely above anything we might make out of our artificial knowledge that
is set up against the knowledge of God, because the knowledge of God is found in creation.
So that virus is going to want to get back to how God made it. And it looks like that's what it's
doing. So the spike protein in the vaccine is different. And so certainly, again, we come to
this world Novavax, we're going to be injecting spike protein, altered spike protein. For those
who think the Novavax is safer, you're still getting a spike protein injection,
altered spike protein, and you're getting lipid nanoparticles.
And you're getting another immune adjuvant, they call it matrix M,
it's a saponin, it's a plant soap based irritant to create the antibodies.
So, so yes, so I think that's, that's about that story there. Until we get into into next week,
we're going to talk about, talk about the the side effects in the different categories and
all the things that people can do and hopefully find some people who need to need to get a bit
of help. So any other questions people you can unmute unmute now we've got let's just do 10
minutes just straight unmuted and you fire away. I've horrified you all again.
I put one up there as well, that what I've heard is the graphene oxide, the
um because it's conductible that with the 5G like what I've heard about the 5G towers is that it
emits certain things and it's part of what they're already using in certain behavior modifications to
break up you know crowd control and things like that around the world. This is where we get into
speculation. The fact that I can give you is that graphene oxide is highly conductible.
The fact that I can give you is it does react in the presence of 5G because it is highly
conductible. The fact I can give you is that these vaccines, the graphene oxide especially
they're small enough nanoparticles cross the blood-brain barrier and can get into the brain.
The fact that I can give you is that the graphene oxide as part of your vaccine carrying capacity
and adjuvant capacity are in the lipid nanoparticles which can also cross into the
brain. So yes graphene oxide will be in the brains of people who've been vaccinated,
yes graphene oxide interacts or I should say 5G interacts with graphene oxide.
Beyond that we don't have proof it's speculation but
yep I've heard I've heard people you know say that you know like but I don't know who these people
are like I don't know who these people are like but I don't know who these people are like.
they might say they're a scientist, but I don't know who they are. So it's like, okay, whatever.
So like I said, unless you can confirm thing. Yeah.
Yeah. At this point in time, we've got to say that all that is speculation.
Yeah. Yeah.
Does it fit with the overall picture of everything else that's going on and all the talk of AI
and Klaus Schwab's talk that, yes, you're going to have nothing and you're going to be happy.
Well, why are we going to be happy with nothing? Well, maybe because they've already managed to
wipe out significant parts of our brain under the influence of lipid nanoparticles and
graphene oxide and 5G that is going to be used to manipulate us. That's all of that.
There is an awful lot happening now that used to be in the realms of sci-fi,
but actually on the edges of what is already possible science, what is already science and
what is. So do we have proof? No, we don't. But do I disbelieve it? No, I don't.
Yeah. Because I've spent years of looking at cutting edge technology and listening to people
like Tesla guy and looking at what they're doing. And so this is just playing out of what I've been
saying for the last five or seven or eight years. And it's like, okay, I never understood the
platform before of how they could make 5G and not need a phone. That's right. But now it's making
sense. Yeah. Okay. Now it makes sense. Again, you know, I mean, like you, I've been, obviously I've
been in the integrated field for 35 years. I've been in the outlier of the integrated field for
35 years. I've been looking at all of this stuff and watching it coming. I knew all this was coming.
I'm not surprised, but what I am surprised is that it's five years sooner than I thought
and being rolled out with the rapidity that I didn't quite expect.
So we, I don't think, I don't think we can afford to let ourselves be surprised by anything
that that might come. Even though we might not yet have proof of it and we might not be able to say
directly, they are doing this. There's enough around the edges, you know, so I'll say if
there's smoke, there's a fire, you know, if something smells this, there's something wrong
there. So, so does he smell most definitely? Is there lots of smoke? Most definitely.
Have we found, you know, have we got to be, have we nailed it exactly? Well, no, we haven't.
They've got a long time on us. They're, they're streets ahead.
God knows. Could I ask a question? Yeah. So I, I, I've just been, you know, like really wondering
that so many people they're not willing to look into this and they just want to, you know, do
whatever the government tells them. And so they're willing to hear what, what is in the vaccine. But
in the vaccine, but at the same time, you know, like they're, they're not motivated because
you obviously see a lot of people that are, that, that have taken the vaccine and
they said, Oh, I was just, I just had a headache for a couple of days and then I was fine. I was
wondering if, you know, like we've seen cells that deteriorated after the vaccine. I'm just
wondering if there has been any studies or I guess taken samples of people who have had
minimal reaction from the vaccine and they've taken a sample of the cells and see what's
happened in the, in, in, in the cells. That's a really good question later on a couple of,
well, certainly for my, just in my patients, for example I routinely test, have been looking at
what we call T cell subsets. And I've got numbers of patients where, where we've seen
some unfortunately where the T cell subsets and lymphocytes have continued to drop despite what
I've been doing. And I've got to ramp up what we're doing and find the ways to stop that process.
Others where they, they dropped, but we've been able to reverse it. So that's just, you know,
your immune markers with regards to the heart. This was the work of Peter. Actually, I don't
think it was his actual paper, but Peter McCulloch presented a paper where, where they
did cardiac MRIs on a whole heap of people. And a lot of those people did not present with chest
pain, but were just a little bit tired. That's all. In every one of those people, everyone,
without exception, the cardiac MRI showed evidence of heart damage. So I think in a lot of these
people, in fact, this is one message I was going to be talking a lot more into next week.
The message has got to get out, but if anyone is feeling overly fatigued, and particularly if
they've got any shortness of breath or any chest pain, they really must get a cardiac MRI done.
If they can't get a doctor to listen to them, fork out the money themselves and get it done
privately because you can. It costs you a million dollars.
about $300, $400. But I believe that there is going to be a large amount of undercurrent
pathology that people will be, that standard, even people going to their standard doctors
have just been told, oh, look, this is normal, there's nothing to it. So standard doctors
aren't testing. They don't want to know. And standard people are just putting, brushing
things aside. So that is going to come out more. There already are hints of it. As I
said, the cardiac MRIs we've got. So the big problem we have got, we've got two big problems,
I guess, but the big problem we have got is that a large part of the medical community,
like the rest of the public, are blinkered, severely blinkered, sound asleep. Either because
they are just so afraid that they don't want to take the blinkers off because they don't
want to see what they're going to see. Or because, yeah, they're just plain sound asleep
and just don't want to wake up. But the numbers of medical, medicos who are waking up is growing
around in Australia, New Zealand, well and truly around the world, it's growing. So I
do believe this year we really are going to see that erupt.
And if they do get a, sorry, if they do get a cardiac MRI, what would happen then? Do they get
referred on or, because they can get the test, but I think people, what I'm hearing is they're
getting sent for all these tests, like friends who have got immunocompromised, even if they
think it's the vaccine, they're still going everywhere, but nobody's actually telling them
how to, you know.
That's why they need to connect with places like the COVID Medical Network,
you know, who's got doctors who know how to treat these things. I mean, you know, I'm in there,
but I'm overloaded, unfortunately, so, you know, so wait. This is our unfortunate problem. The need
is way greater, way greater than the numbers of doctors we've got. But yes, so in a sense,
yes, help can be had. But yeah, it's hard to get into us, you know. But that's part of why next
week, I want to talk into a lot more of what can be, what the side effects are, what to be looking
for, and a lot more about what can people do to treat that. Because that's really what we've got
to do is get the message out that way of what are the things people can do, you know, to treat
themselves, because there aren't enough medicos out there to do it. So curious, Robin, on an ECG,
what do you think, Jo? Not usually. You can have a totally normal ECG, you can have totally normal
standard bloods and still have a problem that will show on the cardiac MRI. So it's a matter
of severity. Okay, it is a matter of severity. It may show on an ECG, but not necessarily.
And another one, are you concerned, like about particular people who are really well connected
with the government or with the police actually coming on to this and hearing stuff? Because I'm
a little bit wary when I know people are so well connected, if they still seem to be asleep,
even if they know that they've been vaccine injured?
Look, I'm at the stage personally, where I know I'm going to get done at some stage.
I know that. They can't take my license, I've already surrendered that. So I am not afraid
of speaking out anywhere on anything. So if people know someone who should be hearing this
either asleep or whatever, if they'll come in and listen, great, I'll go for it. Okay, wonderful.
Thank you. I'm okay. And I'm sure we're all praying as well. I've died once, been sent to
heaven and been sent back again. I've had more than one death experience. I should have been
dead multiple times over. So my time isn't finished. God will keep me here as long as
he wants me here. I'm not concerned. I'll be protected as long as he needs me protected.
So we just got to do what's got to be done. So go for it.
Yeah. Robin, can I just ask one quick question, please?
Okay. I have a friend who had the jab and the whole family and she got COVID.
Her kids, everyone got over it in a week. She took a bit longer.
But now she's telling me that she is battling with extreme, extreme fatigue.
She needs to see if she can get her to come in next week and tell her story and then she
can listen to everything and then we can point her in a direction.
Okay.
Yeah, problem is she's in country Victoria, far north.
Well if we, this is something that I know at least we were trying to figure out with
Elyse, how we can actually get away, see if we can't, we're not going to be able to physically
get everyone.
My two people I can't physically get in here.
We're going to find a way to do this during the week so that we can for, you know, whether
we set up a particular Zoom link just for next week, whether we do that, I think that
might be the, you know, while Elyse and the system are thinking we'll do a Zoom link just
for next week, that'll be, it'll be obviously be a bit more open, but you know, cool.
That's what it needs to be because these are the people we need.
She needs to be able to hear other stories, right?
She needs to hear other stories so that she feels validated.
Everyone else who's coming in, you know, needs to be able to tell their story so they're
validated.
And then they need to be able to hear, now look, there are things that we can do.
They need to hear that this makes sense.
Why this has happened makes sense.
They're not imagining it and that there are things that we can do.
So please, everyone go for it.
Anyone you find like that, you know, Elyse will work on it and get a separate Zoom through
the week, but let's get as many in as we can.
Okay.
How early, just some feedback, do you need the new Zoom link?
Would it be handy to have by the end of this week or is it all right to give out on Monday
or just the day before like they have been doing?
Unmute and let me know what you need.
I think I need a few days, I think, but yeah.
Okay.
So I'll send out an email tomorrow with a new Zoom link, it will just be for next week
only that you can share with everyone, okay?
Yeah.
Excellent.
And can I just check, you said if anyone is really tired, plus a shortness of breath
or something, what was the second thing, I missed that.
Chest pain.
Thank you.
Yeah.
They certainly should get it checked out.
So I saw a printout and it's almost time for us to finish.
I saw a printout from South Australia, I think it was, a South Australia ambulance, you know,
all in for one day, hundreds, purely chest pain, one day.
Chest pain, chest pain, chest pain, chest pain, chest pain, chest pain, chest pain,
chest pain, chest pain, chest pain, chest pain, chest pain.
Incredible.
So, yeah.
So let's see who we can get in and pray for them ahead of time yourselves, you know, be
praying so that anyone who comes in, you know, that their eyes can be opened and they are
helped.
And if we can, you know, even if out of that we only get a couple more open, okay, let's
get a couple more open, we get a couple more helped, you know, then they might spread the
message to their friends because they're likely to be in the vaccinated groups.
So let's get the message to their friends, even if it's just some who've been vaccinated
and then likely, you know, then, oh dear, we've all had COVID and COVID again.
It's like, yeah, let me tell you why the vaccine doesn't work against COVID.
Yeah.
Some people are asking, the Zoom meeting will be recorded as usual and I can send the link
out via email, which you can pass on to them via email.
It's just a Google link.
So that will give them access just to that one, not to the group.
So we can do it that way, okay.
Yep.
That'd be great.
They'll have access just to that one.
Yep.
Very good.
Okay.
Wonderful.
Well, let's look forward to that and getting, you know, a full thing here so that we can
get people in.
And I'm sure that'll be one that'll be able to be replayed and the link for that again
sent out for people who want to look at it later.
Yeah.
All right.
Bless you all.
Time for us to finish up and see you next week.
Thank you.
Bye.