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Dec. 22, 2023 - Stew Peters Show
54:45
Uncensored: Russian Study Finds Connection with Nanotech & COVID - Dr. Ana Michalcea
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We'll be right back.
We'll be right back.
from and certainly not the Stu Peters Network either.
This is a topic we've confronted head on for a very long time now and we're grateful for all of the truth tellers around the world that are giving their contribution to it.
What I would say is that this is still such an unknown field.
And so all of the people that are helping put these puzzle pieces together are vital in humanity understanding the real goals of transhumanism.
Dr. Anna Mahajcha recently shared a Russian study which found self-assembling nanoparticles and nanofibers actually associated with COVID itself, which is very, very interesting.
And so she's going to come on in a moment to discuss that.
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And here is Dr.
Mahaicha now.
Dr.
Mahaicha, thank you so much for joining us today.
We really appreciate you.
Thank you.
Thanks, Maria, for having me again and for allowing me to explain some new findings.
Yeah, absolutely.
You know, I've done another recent interview with Dr.
Nixon and Carl C. And what it looks like to me, Dr.
Anna, is that things are changing.
The human body is changing.
The nanotech seems to be becoming more advanced.
And naturally, my brain, my logical brain says if the nanotech is becoming more advanced or changing form or, you know, the functions of this would also be becoming more advanced inside.
It's something that we're still investigating, but I think needs to be spoken about openly.
So what is it that you want to share with us today?
So I have done some research recently on antidotes like methyl blue and how they're working as well as really what is polymer science and how can we think about these clots in relation to the amyloids and prions.
So I've prepared a presentation just to be able to show people what's recently come out in the scientific literature.
In fact, some of the articles are Our preview, they have not yet been peer reviewed, but I found them so interesting that I absolutely wanted to talk about them because they're so fundamentally important for the work that we've been presenting over the last couple of years.
Great.
Well, let's get straight into it and we can discuss as we go through the presentation.
Wonderful.
So this is really explaining this gain-of-functioning engineered spike protein, which remember I was, and Karen Kingston also discussed, this is really artificial technology and that it is a coding for self-assembling nanotechnology and what have prions and amyloid and hydrogel to do with any of this.
So this is a very interesting new article that was just posted on December 9th in the Archives of Biochemistry and Biophysics, and it discusses that self-assembling amyloid-like nanostructures from SARS-CoV-2 And S1, S2, RBD and N-recombinin protein.
So the reason why this caught my eye, and this was actually discussed in the Thailand Medical News, was because of the wording of self-assembling nanotechnology.
So the researchers remarkably uncovered That there were self-assembling nanoparticles and nanofibers of varying sizes that developed, which is exactly what we have been finding and have been talking about all along.
And what they did was that these solid protein structures We're stable, so they weren't degrading, even though they thawed them, they froze them.
They thawed them, they froze them.
They actually did it over three years, and these things did not change.
It says two years over here in the original paper.
It says three years.
So what is interesting about this is that They analyzed these structures with very complex methodologies.
What happened is that the nanostructures do not look like virus-like particles.
What are virus-like particles?
They are also engineered particles That sort of have, you know, similar effects like viruses, whether or not you believe in that or not, but it was very interesting because they found amyloid-like structures and they were suggesting again that the self-assembling nanostructures have something to do with the proteinopathy in patients.
Proteinopathy means You know, coagulation of proteins, like these rubbery clots that we've been seeing.
So this is a very important paper.
We'll see if it survives peer review.
But the reason why it is important, again, is that That there is an interplay between the nanostructures and the human body, and that that really is a key to understanding how it's affecting humans neurologically.
And then they're also saying, well, this is also affecting the vaccine development, because obviously the same sequences that are creating these self-assembling nanostructures are also related to the vaccine.
So this was an interesting discussion.
Even the diagnostic accuracy aspect and acknowledging that, okay, so there are these self-assembling nanostructures.
What does that actually mean for diagnosis of SARS-CoV-2?
So very, very interesting.
Yes.
So, you know, they gave a lot of images and clearly, you know, went into an endeavor to investigate what these nanostructures are.
And what's very interesting is they were not the first.
So this particular article has already been, you know, peer-reviewed, and it shows that the SARS-CoV-2 spike protein creates amyloids, so this misfolding of proteins, and that there were seven sequences found.
And that it acts like a polymer.
So what's a polymer?
A polymer is the same thing that I've been talking about, you know, for a couple years.
It's a self-assembling nanostructure that is used in biotechnology and in nanotechnology.
You can have natural polymers, like protein, or you can have inorganic polymers that, for example, create nylons or microplastics.
So this is important because these polymers created these amyloid-like filaments, which is, you know, remember the filaments that you see right behind me?
And the reason why we should even think about it is because it is said in medical literature that these misfolded proteins have a huge impact on stuff like Long COVID,
chronic fatigue, neurological abnormalities, you know, SARS-CoV-2 people who had maybe the illness that they are then Experiencing things like prion disease,
which is also misfolded proteins, and then really saying, okay, there is a correlation between the infection and the vaccination and the fact that amyloidosis happens.
So I find this a very interesting and important topic, and I want to discuss it from the perspective of the nanotechnology application.
So I've spoken about this particular article for a long time now because when my colleagues were saying that the spike protein is creating amyloid, I was saying no.
Science has shown it's creating hydrogel.
And in this paper, it's been shown that at pH 4, which is very acidic, amyloid happens to be made.
But at pH around 7, which is where the body is, hydrogel is being made.
So it has been proven that the synthetic sequence of the spike protein that we know is man-made It's creating hydrogels.
And what are hydrogels?
Remember, hydrogels are programmable matter that are used for the brain-computer interface.
Hydrogels are used as polymers for biosensor application that are used for interbody network remote control of humans and remote sensing.
So this is a very important correlation here that people keep forgetting to speak about.
Now let's get a little bit into the fact that these self-assembling peptide and protein amyloids, so basically a peptide is just a small sequence and a lot of these peptides create proteins which are essential in the body, but you can have actually Other proteins like wool is sort of like a protein polymer, for example, and I'm going to talk about polyamides here in a little bit.
So peptides and proteins That create amyloids in the human body are actually being used in nanotechnology now.
And so as advanced materials in biomedicine, tissue engineering, renewable energy, nanotechnology and material science.
Because of how they're folding themselves.
And they're saying, well, they're biocompatible, meaning you can inject them in the body and there doesn't seem to be much of an allergic reaction.
Except, you know, they create these clots and they literally create amyloidosis in the brain to make people have dementia-like symptoms.
So in terms of dual purpose, you could see how that could be misused.
Yes, absolutely.
I've been reading about You know, programmable matter and nanotechnology used in, you know, therapeutics for some time now.
They don't talk about it.
They don't hide it.
They just say it's really good because you can program it to target specific illnesses, for example.
They don't hide this tech.
No, they really don't and it's very unusual to see how much in denial doctors are because it is absolutely common in the literature and it's used in cancer therapeutics, all kinds of areas.
So if you're seeing here that these amyloids are used also for functional nanodevices, so they're building technology.
They are building hydrogels for cell culture and drug delivery.
They're building biosensors.
This is the whole area of what we've been talking about.
And functional materials that are biocompatible, meaning you can inject them in the body without it getting rejected.
But they have biorecognition ability, so that can also be, you know, such surveillance and energy conversion materials means they can hijack your energy to actually use the human body as a battery.
Yep, which they also publish and brag about.
Absolutely.
Human beings are a battery.
They've said it.
And openly spoken about how the human being's energy will be used to power up the wireless body area network.
They've said this.
Absolutely.
So we understand now that amyloid nanofibrils are used for this, and this is out of the same article, and you can see this is a micellar, which is, micelles means little round, little amyloid structures,
and they create these long structures, and this is from my clinic, an unvaccinated individual, and you can see this Micellar appearance, which is, we're talking about how things have changed lately.
We see a lot more of these bubbles that some people are saying are air bubbles.
They're not.
They're filled with these little tiny And from that, they are building these structures, these hydrogels.
And now we can understand, okay, wait a minute.
They're just saying that these things are actually aspects of building nanotechnology in the body.
Very interesting.
You know, you can see the two commonalities here just from a visual perspective.
I'm not a microscopy expert.
It's different forms, different types of microscopy being used.
So, you know, certainly interesting to consider.
Absolutely.
Amyloids have been used, for example, here in amyloid-based textile composites that are used as wearable pH sensor skin patches.
So again, biosensors for healthcare and fitness industries.
They've been used again in cell culture, tissue engineering, and drug delivery.
And what is very interesting is, remember what we've been talking about is all of these blinking lights that we call quantum dot structures, micro robots.
Well, it turns out that amyloid has very unusual photoluminescence.
Properties, meaning it emits light in different frequencies in very interesting ways, which makes it a great material for biosensing applications.
Amyloid hybrid quantum dots have been used as nano assemblies, for example, to probe neuroinflammatory damage.
So we've been talking about quantum dots and how they are Very important in biosensing applications.
Again, this is a preview, but it's just very interesting that now amyloid is coming more and more into the biotechnology field, and that happens to be exactly what is making people ill after the shots.
So remember quantum dots, this is a slide or a microscopy that I've shown from a COVID-19 unvaccinated individual who came to my office and you see how these biosensors are photoluminescent, meaning exactly what I just said about the amyloid, they're emitting light.
And there are structures that are larger than quantum dots, so I would almost call this a micro robot, but nonetheless, this can be used for bidirectional telemetry purposes.
And just to explain what that means is meaning that your internal physiology is being monitored and sent to the cloud, but that you can also be accessed via frequency and modulated.
Well, just to add to that, they talk about the fact that, you know, AI health will replace doctors.
And when you look at the biodigital convergence documents, they openly talk about how AI is going to sort of constantly have a sense of how to, for you to maintain your optimal health and therefore It'll tell you in the morning what supplements you may need to take, or it'll administer them remotely via the quantum dot technology in your body.
It's an AI doctor, essentially, that's constantly monitoring your health in real time.
Lisa McGee and Todd Callender were on with me recently and Lisa said she saw that the WHO had a database where in real time these sensors inside of people were sending data back to the WHO. Absolutely.
And I absolutely am so grateful for Lisa's and Todd's research.
And it's been corroborating everything that I also have been saying.
And what I just want to explain to people, you know, who say, oh, this is sci-fi.
Look at this article from 2003 that, again, is discussing that you can make microchips that are hydrogel protein-based.
And so these microchips are exactly what Dr.
David Nixon and myself and others have found in the vials, and now we've found it in many medications as well.
And, you know, this has been around now for two decades.
And has been perfected to affect humanity, and this is exactly what we're finding.
So people cannot be in denial of something that has been around for this long.
Here is an article that discusses functionalized prion-inspired amyloids for biosensor application.
Now, prions, remember, that is related to highly infectious particles, That can shed from one person to the other and cause things like mad cow disease, Creutzfeldt-Jakob disease, that basically eats up people's brain and creates zombification.
Isn't it interesting, you know, for the fact that if the WF wants mindless consumers and they want to absolutely control things, that we are finding prions and amyloids that target the brain so that people that we are finding prions and amyloids that target the brain so that people I do not think that's a coincidence.
And the fact that they're literally using these prions, number one for biosensors, and that we know that these nanotechnologies are transmissible.
They're shedding.
This is clear from the shedding data from Pfizer.
Remember that in the Pfizer document it said that an unvaccinated man who inhales the air around a vaccinated woman can then take that intervention or vaccine to another unvaccinated woman and transmit the vaccination status.
Yeah, it also says that they can be subject to adverse events from exposure, just contact.
So we're talking about this person being intimate with someone who's injected and the uninjected person potentially having myocarditis.
Pfizer says this can happen.
Absolutely, and I've seen that, actually, in my clinic.
Polyamides are polyamino acids, and they are used for drug delivery.
And the reason why this is very important is because Plobber-Carnicum has shown that the rubbery clots are made from polyamides.
And I just want to explain here this patent.
So this is a lipid nanoparticle compositions and methods of formulating the same from Moderna.
And what it shows here is secondary amines.
Amines are polyamides.
And that is what we found in humanity's blood is constituting the clots.
So this is part of their lipid nanoparticle composition.
And then the other thing that I found in this patent was this part, which shows that in some embodiments, the lipid nanoparticles described here are stealth nanoparticles or target specific stealth nanoparticles.
And that happened already described in this previous patent.
So what they're saying is, These target specific nanoparticles can comprise a polymetric matrix, which comprise two or more polymers that are such as, but not limited to, polyethylene.
So that's polyethylene glycol.
It can be polycarbonates, polyanadrenes.
But look at this, polyethers, polyesters.
So these are plastics.
Polyvinyl alcohol is vinyl plastic.
This is what we found as signatures in people's blood.
Yes, I remember.
This polystyrene is styrofoam, polyurethane, you know, polyamines.
You see this polyamines right here, which is what Clever Conicum and I found.
So these polymers are plastics, microplastics, and we are having a microplastic epidemic or pandemic worldwide.
And what I want to explain is that these same polymers and plastics are modified to create biosensor materials.
So here it is.
And this is supposedly environmentally friendly, but you cannot dissolve this stuff.
And what are they using in medical biosensors?
The same chemicals we just saw in the Moderna patent, polystyrene, polyethylene, all of these things, polyamides, are part of biosensing technology, nanotechnology.
So again, I wanted to explain terminology.
So amyloids and pions are misfolded proteins, and polyamides can be peptide chains.
And polyamides, they can either be natural, for example, wool and silk, or artificially made, which are nylons.
And so it's important to kind of understand that, because nylons, you cannot break down.
You know with acids and all kinds of things so remember this is what we found in as the chemical signature of cross-domain bacteria as well as in the blood in vax and unvax.
So here's your polyvinyl alcohol that's a plastic Here are your polyamides.
This is either nylon or it can be other protein, misfolded proteins like the amyloids.
Here's the polyenes and alkenes.
That's your polyethylene glycol.
And then we also found silicone, which is used as a transistor material to create biosensors.
So the signatures certainly are matching.
And then remember the clot analysis.
So we had three forms of clots from the deceased individual, from a vaxxed-injury living person, from an unvaccinated individual.
And this is a rubber-like material.
And the microscopy shows these filaments that Climber Chronicum discusses are CDBs.
I believe they're technology now.
And you see that the same signatures occur.
These aromatic amines, the polyins, the alcohols with vinyl, plastics.
So this stuff is all consistent and you cannot break it down as I discussed on your show before.
Now what's really interesting and the reason why I'm mentioning this again It was a world-renowned scientist, Dr.
Diana Wojtkowiak from Poland, who actually went to the Polish parliament and accused them of genocide after she investigated many different medical supplies like insulin and heparin.
They all had graphene in them.
So she was following my research and she did what's called a torsion spectroscopy on the same rubbery cloth.
So torsion spectroscopy can tell you what elements are in there.
So she found hydrogen, carbon, nitrogen, as well as copper, selenium, and zinc.
But what was so interesting was her conclusion of her analysis.
So she says that in this spectrum, it is evident that the signal of a prion-like protein predominates in the clots.
The characteristic signals for prion-like proteins are copper, selenium, sulfur, and elementary particles from the prion-led nuclear reactions, aromatic amino acids, which are the building blocks of these proteins.
And she says that we know that prion-like proteins form pseudocrystals, which look like microchips, and they form fibers that you can see in very large dimensions, which you can see behind me.
And they are resistant to acid, alkali, detergent, and normal methods of dissolving clots are useless, which is exactly what I've been saying.
So here's another world-renowned scientist who is confirming what Clifford Konikin and I have been saying all along.
And here is proof.
This was a case history that I had posted of an unvaccinated individual who had blood clots in his legs, later developed life-threatening blood clots in his lungs.
Remember, unvaccinated but exposed to shedding.
And has been on Eliquis, which is a very broad-used blood thinner, a strong blood thinner.
It was using netokinase, lumbrokinase, and serreptase.
And still, when we just drew the blood and let it sit, 30 milliliters sit overnight, you can see this hydrogel rubber-like clot material develop.
And so this is exactly what Dr.
Vorkowiak also has been saying.
It's like the prion-like material, polyamide protein like nylon or, you know, it can be an amyloid.
These things you cannot destroy with regular blood thinners.
So I just want to briefly remind people that these micelles in the blood contain other little tiny particles that then are growing and then are growing these filaments and they're self-assembling to very large structures.
And ultimately the reason why this is also important is I believe That the literature really has been discussing everything that I've been saying, but they've been calling it microplastic.
And the reason why this is important to really look at, so this was a study where they've looked at microplastics in patients who underwent cardiac surgery, and they looked at the human heart tissue and the myocardium, the pericardium, the fat around it, And they found many microplastics and nine types of them.
And what were the microplastics?
Polyethylene, polyamide, polyvinyl alcohol, polyurethane, polystyrene, polycarbonate.
All of these are on the Moderna patent as stealth nanoparticles.
Dr.
Anna, just yesterday I was speaking to someone who said, wouldn't they detect this in x-rays?
Wouldn't they detect this?
Wouldn't cardiologists be detecting this stuff?
And I said, it's presenting to them in their medical brain as something, they're understanding it as something that it's not.
Yes.
This article is an example of that.
This is why I want to explain that different words are used for similar things.
I believe that microplastics in human bodies is the same thing as self-assembling nanotechnology.
The healthcare freedom movement is saying amyloid and prion disease.
I'm saying it's self-assembling nanotechnology.
Either way, we have to understand that we're talking about the same thing and that the methods of addressing it need to be coherent.
And I'm going to talk about this in a little bit, but you can see that Clearly here, I mean, look at, this is some pretty large microplastics that were found in the human blood, and this is reputable scientists that are saying this now in the scientific literature, but regular doctors will not read it because it's in the Environmental Scientific Technology Journal.
Right.
So here's the compartmentalization.
I also want to mention, because we're talking so much about turbo cancers, that it's been clearly shown that microplastic polymers are related to causing turbo cancers, accelerated aging in all diseases.
And the toxicity of polystyrenes, polyurethanes, Are clearly related to these cancers.
And for example, in cell cultures, you can create a cancer in 24 hours by exposing them to these microplastic polymers.
Even though they have not been categorized as cancerogenic, not all of them, but there has been very good literature.
And in this article, I've reviewed that.
So it's very important to understand again, you know, here are the many doctors who are just saying, oh, we're seeing all these turbo cancers.
I've seen turbo cancers in the unvaccinated because I have contaminated blood and they're dead in three months.
So it's very concerning.
We need to keep cleaning the blood.
This is a very important part of the research.
So I took budesonide, which is, by the way, an inhaled steroid that people have been using for COVID symptoms.
And I clearly found these micro-robots, as I call them, you can call them quantodots, whatever we call them.
So they're part of the problem and they're clearly made from polymers.
They are light-emitting and they're moving, also self-assembling, self-propelling.
And I've photographed this.
This is a 4000 time magnification of a micro robot and how it's emitting light and how it's moving.
And you see it's micellar structure.
So what's a micelle is these round bubbles.
So this is in Budesonite.
People were inhaling this stuff.
And I did a test to figure out if methylene blue would help bind it.
And what I saw was methylene blue would bind these filaments and then all of a sudden these micro robots were attaching to it.
So I was like, wow, this is very interesting.
Then I looked at insulin, because remember, I scared the whole world when I said insulin has this stuff in it, the hydrogels, and I've shown that.
So what was very interesting, I took Lantus, and I just looked at it under a microscope, so similar nanostructures and filaments were immediately visible, and you see that Because there is a polymer in the lantus, as I had discussed previously on your show, that clearly is growing these filaments.
So what was interesting was I left the insulin sit for 24 hours, and then I re-looked at it, and it actually did create microchips and crystals exactly like the dental anesthetics that we've had.
And so you can see these are similar structures that we've seen in multiple other drugs.
Dr.
David Nixon has shown this.
We've seen this from the vaccines.
And you can see that overnight there's quite a bit that had developed.
So then what I did was I mixed the insulin with methylene blue and initially it was just kind of looking like this and literally just a few hours later this happened.
So the methylene blue concentrated itself and it was magnetically attracting the polymers and this material.
What is methylene blue, Dr.
Anna, and why would it have this effect?
Okay, so methylene blue is an ultraviolet blue dye that's been around for 100 years.
And it's been used for staining applications, but in medicine it's used for what's called methemoglobinia.
It's something, you know, where people need help with oxygenation.
But it has been shown to have remarkable effects, for example, in helping Alzheimer's, Parkinson's.
It is an electron donor to mitochondria, so it's used as an anti-aging molecule.
It has been shown to increase the oxygen delivery to cells between 30 to 70 percent.
And, for example, there were studies in mice.
They did give the mice a cardiac arrest.
They left them dead for 30 minutes, and they then resuscitated them.
The group of mice that got the methylene blue had no brain damage, which is unbelievable.
So Methyl Blue has had some amazing anti-aging effects and I've used it for a long time because it's the precursor molecule to hydroxychloroquine.
It is a precursor molecule to a tricyclic antidepressants which actually so it has mood elevating effect.
It has pain relieving effects.
So it's something that you can get over the counter.
My understanding is it can also be toxic as well to people.
Is it like certain doses?
So the only toxicity or contraindication is with people, for example, who are on serotonin reuptake inhibitors, meaning antidepressants.
But in general, it's been used in the integrative community for a long time.
I've used it for many years excellently in regeneration of neurological diseases.
So remember when I talked about the EDTA and all kinds of people were coming out saying, oh, she's poisoning the world with EDTA. These people have no idea.
A lot of people start speaking up.
They don't have medical education.
They don't have any experience in treating patients.
I would just be a little bit careful because we're endeavoring to find solutions for the world and for technology.
Let people who have the scientific knowledge actually You know, educate you a little bit.
So there's a lot of books about methylene blue.
Thomas Levi, a well-firmish cardiologist, has discussed it.
So it's been used for a long, long time, very safely.
I've never had an adverse effect with anybody.
So here's what happened the next day, which is that all of the polymers actually went towards the methylene blue and attached themselves to it.
Here you can see this in a higher magnification.
So it clearly also had the same effect with insulin.
And the reason why methylene blue is interesting is because it's been very well researched for prion disease, amyloid, As an amyloid inhibitor, as well as I've shown how it helps prevent the rubbery clot formation.
And, for example, in environmental technology, hydrogels are used to eliminate methylene blue from wastewater.
There's a very strong binding, almost magnetic binding, of methylene blue to hydrogels.
So I had the idea, well, why not use it to actually pull the stuff out of the body?
And so here are some of the articles that discuss, for example, that methylene blue binds and prevents the fibrils of prime proteins.
Methylene blue reverses amyloidosis in the brain and improves cognition.
Methylene blue again here inhibits this The making of the polymers and here it inhibits how they are being made.
And so what I did, I did testing with people This is someone who is unvaccinated, who had nothing done to their blood, and I just used the same blood, 30 milliliters, and just put some methylene blue in it, 0.5 cc, and I looked at whether or not it would inhibit the rubbery clot formation.
So I saw that it did, and then what I did was I had the same patient take methylene blue daily, and then I redrew the blood A few weeks later and you can see that the rubbery clot formation is inhibited.
So that's a huge improvement and very, very hopeful.
Yes, so I've done since then had much feedback because some other patients of mine have done Experiments in terms of looking at whether or not methylene blue would inhibit the rubbery clot formation.
For example, I had shown the blood of somebody who was on the blood thinners with a netokinase and lumbokinase and added methylene blue and that actually inhibited the rubbery formation significantly, which is very important for somebody who's already had You know, blood clots in the lungs and blood clots in the legs.
So this is very, very hopeful because Methyl Blue has so many results.
So again, you know, I've used it in my practice for a long time.
I was using it for a stroke rehab patient.
Neurologically, we have an Alzheimer's patient because I used to be a geriatrician, so I've used it a lot.
In older people, phenomenal results.
It does good with helping with the brain fog.
So again, you know, I think that we have to be a bit careful.
If one person dismisses something, that doesn't mean it will not work for millions of people.
Many different clinicians have been working with methylene blue for vaccine injuries now.
And I've heard about extraordinary results, similar like with the Plaquex combination that I've also been using.
And because the FDA recently went after peptides, so pulled them off the market in the United States.
EDTA is on national back order.
You know, we have to find solutions that us medical professionals can use for our patients to help them, as well as You know, educate people about what are the possibilities out there.
Can I ask you, Dr.
Anna, with the rubbery clot formation, so that first photo that you showed in that last slide, was that someone who had been forming clots?
You collected their blood?
No?
No, it is an asymptomatic 40-year-old gentleman, absolutely no health issues, no prior clots.
One of the things that is important to understand is that polymers will polymerize or create the rubber in a temperature-dependent fashion.
So, you know, when you draw the blood and you let it sit, the blood will cool down and that will actually make The rubbery clots form the rubber.
And this is something that I discussed with Richard Hirschman because he was discussing that in some of the people that he was embalming, the huge clots appear to be forming after death.
And only some of them, you know, while people were alive, which makes sense because people were asking, you know, if everything that I'm saying is right, why aren't people falling over dead, you know, with these ginormous rubbery clots?
So there seems to be some external form of activation.
Same thing, for example, our microscopes.
When we're looking at the blood, we're actually activating the quantum dots because there's a light source coming towards them.
So all of a sudden, you'll see them blinking and being more active, which makes them more visible.
So this can explain some of why some people are more symptomatic than others.
However, we know that millions of people have amyloidosis.
I had a 50-year-old patient who died after shedding very rapidly with systemic amyloidosis.
So I think that it's important to find solutions for this and to look at the different possibilities.
So just back to that last example, because I want to make sure I understand even.
So that blood clot that formed, the rubbery clot that formed, it formed after you took that individual's blood out?
Yes, exactly.
So what you do is you turn the blood, you take the blood 30 cc and that blood looks fine.
And all of the tests that we've done is we let the blood sit and to see if hydrogel forms and develops, which is a marker of whether or not there's technology in there that can form it in the first place.
So, and when we are comparing it, we're always, I am always comparing it at the same time frame, taking the blood of the same individual, and then are using certain molecules.
You know, for example, I showed that EDTA inhabits the blood clot formation that vitamin C does, now methylene blue does.
So, it's comparing apples to apples.
That's very, very important in this research.
So you take it out and it forms and it could be various external factors including temperature.
So then how do we know that those things are forming inside the body in the same way?
So some of the things that we're seeing, for example, under the microscope on a much smaller scale, because remember that those rubbery clots, you know, to have a clot of two, three centimeter diameter compared to what we're seeing in the blood under the live blood microscope, you would have to have quite the growth process.
In my scientific colleague group that I was in, there was somebody who had taken the water from a from someone who was using an ionizing foot bath that individual was vaccinated and the water was cultured over a period of six months or more in a mason
jar and actually the filaments continued to grow outside of the body to being visible So this stuff continues to grow, which is in line with Morgellons, which is in line with the fact that I have shown in embalmed blood of somebody who has been dead for eight months that this stuff still self-replicates.
So it uses energy sources from the external environment or, for example, we've shown that pulse electromagnetic fields are actually increasing the growth, that electricity is increasing the growth.
So those things are all factors to consider.
What I'm saying is, though, with this particular example, you've got someone whose blood is It was not a clot.
It was exposed to the outside world and it formed a clot.
Is that perhaps some sort of a link as to how these are forming within the body as well?
So, again, we believe that the technology of polymers grow based on changes, for example, in pH, in temperature, based on exposure to light, to electricity.
It is harvesting energy from the outside.
So that can certainly be part of it.
Absolutely.
Yeah, I think that's interesting.
I wasn't aware that they were actually forming outside.
I know that what we, you know, have seen as soon as the vials are taken out of the fridge, all of a sudden that changes.
You expose it to EMF, that changes.
You know, I know that we've found these things inside the human body.
I wasn't actually aware that they were forming after the person had died, although I remember speaking with you about that person.
Eight months later, the clot's still alive.
And so, you know, for lack of a better word.
And so it's very, very interesting to me to hear that drawing the blood out of a person and that clot forms outside.
You know, and the other thing, Dr.
Anna, that maybe...
You could help with is if people are having x-rays, would this be present on an x-ray?
Or is this the type of material that couldn't be detected on an x-ray?
You couldn't detect it on an x-ray, no.
But remember when I was talking about computerized thermography?
Because the infrared signature certainly was looking differently.
And way back when, when I showed computerized thermography in vaccinated individuals, that that shows some different signatures.
So we have to look at different modalities.
Clearly, other researchers, like I showed with the microplastics, are now finding this stuff.
And it is embedded in the tissue.
This is where, you know, the alarm vial should get off because everything that we've talked about synthetic biology was about the merging of our human cells with these polymer plastic hydrogels.
And that's exactly what This cardiac study, for example, showed that literally the plastics are now embedded in the heart, in the pericardium, in the fat.
So that's part of this aspect.
And one other thing just common to your question is that self-assembling nanotechnology, that's what we're looking at.
So remember that anybody who looked at the vials Who had to, you know, thaw the vial, and by thawing, the growth process started.
Shimon Janowitz was the first one to show that, really.
So temperature clearly increases the growth rate of this technology, and then it becomes visible to the naked eye.
So time is important.
You know, it grows over time.
And then, like I said, when Clifford Connick did the experiment of using low-level electrical current on unvaccinated blood that under live blood microscopy looked clean.
And he applied the electrical current for two hours and it turned into this rubbery-like material.
So the electricity was making the self-assembling nanotechnology grow and transform.
Yeah, I think, you know, the more I learn and the more that comes out, Dr.
Anna, and you're certainly a huge contributor to a lot of these discoveries, you know, the more I realise we really don't understand enough About this technology as regular people, you know?
And I can see why a lot of doctors maybe just, you know, have their blinkers on and not really looking at this because it really is outside of the normal scope and realm of medicine.
It's doing strange things that wouldn't normally happen in medicine, you know?
So I just want to thank you for...
Sorry, go on.
But it is in the realm of technology.
And that's really what we need to look at.
Because just as you said, that precision medicine and artificially intelligent directed medicine is all about this.
Yes.
About interbody area network, about these hydrogels, about the brain-computer interface.
So this is exactly what we're looking at.
So what we're doing is we don't want to become cyborgs in the name of medicine.
Yeah.
And so this is why we're looking at basically aspects of figuring out how to disable this stuff to be able to survive as a natural human.
Yeah, I agree.
And, you know, certainly appreciate all of your research, Dr.
Anna, publishing the solutions that you're finding that are working.
I think the global community really does need to continue doing this.
I want to bring up your Substack for anyone that is not subscribed.
Please go and do so.
AnnaMahichaMDPhD.substack.com This is one of the articles that we discussed today.
Very, very important.
I actually shared this on X and said, we've been telling you for years!
So, I'm really grateful, not only that you post your findings, but that you post, you know, correlating findings such as this one.
So, Dr.
Anna, thank you very much for your work.
We appreciate you.
Thank you so much for having me.
Thank you to everyone who has tuned in today.
Next week is Christmas and so we will be doing a couple of re-airing of some very, very important topics that I've done on Biodigital Convergence on this very broadcast.
So please make sure if you haven't seen them, watch them.
If you have seen them, watch them again and share them.
Because it is related to today's broadcast.
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