TruthArchive.ai - Related Video Feed

Speaker: A lot of the analysis techniques that were being employed now on the white clots. And about three years ago, there was one piece of analyses that I came across just by accident, which was a thing called an ICP analysis, which is an analysis that determines the elements present in white clots. It was done by a gentleman in The USA called Mike Adams, who presented the findings of his initial white clot analysis from samples that Richard had provided him some almost three years ago now. And it surprised me what the findings were, because I have used the ICP analysis. It’s called Inductively Coupled Plasma Mass Spectrometry. Don't worry about the name. It's just a very well known piece of analytical equipment that you can rely upon to tell you what elements are there in the white clot and in what abundance. And what surprised me was in the analysis that Mike presented was a very the highest element they found was phosphorus, followed by sodium, tin, and later on sulphur, and carbon. And we also found that there were no normal blood marker elements present in the white clots. So, we've actually employed two laboratories in Europe, and there's a long reason behind that because I'm associated with people in Europe who do this kind of work. Anyway, we sent clot samples, they all ran ICP analyses. They found exactly the same results that Mike Adams found. We found aberrantly high levels of phosphorus, we found aberrantly high levels of sulphur, tin, sodium, and carbon. And being an organic chemist, I know a little bit about tin chemistry, because I used to sell tin catalysts, believe it or not, for polymerisation reactions. So I had to study the chemistry of tin. And I wondered why tin would be present in a white clot. So, obviously, we could not believe this first series of results. It's set about replicating the results in two separate labs, and they came back and said, you're right, there's high levels of phosphorus, tin, sulfon, carbon. So the next thing we did was to do an analysis called HPLC, High Performance Liquid Chromatography. And what this does is actually pulls apart the white clots and tells you what the protein components are. And surprisingly, we found that the highest level of proteins we found was fibrinogen. But the HPLC analysis actually will determine what kinds of fibrinogen chains are there. In a normal red blood clot, there's normally one to one to one ratio of the alpha chain, beta chain and gamma chain. We found in our white clots that the beta chain far exceeded the alpha chain and the gamma chain. And in fact, it was beta gamma alpha. So the alpha was the lowest proportion. Now, we're not biochemists, and we're not medically qualified in any way. But we can do simple research to find out why the fibrinogen content was so high. Fibrinogen forms fibrils. This is exactly why when John O'Learny first described the white clots as being calamari like, he is exactly correct. That's exactly the texture that fibrin will bring into a white clot. Okay, so from then on, we then ran some amino analysis results. My colleagues ran an amino acid analysis, and they found a high level of Praline, Aspartic acid, Lysine, a whole range of about 18 amino acids, all that have a phosphorus affinity. And as we said in the white clot, the element that has the highest concentration that we could confirm is porpoise. If you take time then to research the aberrant pathways that what they call excess phosphorylation will cause, it causes a whole range of problems in the human body. So we have determined, we think, the pathway to the formation of these white clots. We have three separate pieces of analysis, all confirming our findings. So we've now pieced together the formation of the white clots, and I'll come back to the very beginning. When we administer the injections, there is a lipid nanoparticle carrier, it's called a phospholipid. We found by our analysis that when the phospholipid releases the mRNA core of the lipid nanoparticle, at the very moment that it releases the core, it actually exposes a phosphorus head of the phosphorus lipid. The phosphor lipid reacts within the bloodstream naturally formed fibrinogen, and that's what's nucleating the white clot formation. Now we can prove all this. We've actually got over 200 peer reviewed papers confirming the pathway that I'm describing. And more importantly, once that initiation of the DSPC now the actual phospholipid that is encapsulating the lipid nanoparticle is a phospholipid called DSPC. I won't go into the name of it, but what it means is that that particular phospholipid we found, again through research, that it will liberate 80 to 90% of raw phosphorus heads as it releases the mRNA core. Those phosphorus heads all react with the fibrinogen in the bloodstream and they cause sandy blood. The reason you guys are seeing sandy blood and coffee grounds is that's the nucleation pathway to the final white clot formation. The other factor we found and proved the spike protein bonds to the phosphorylated fibrinogen. The body is generating methylcetiopridine generated spike, that spike in the bloodstream then starts to coagulate with the phosphorylated fibrinogen, and that feeds what we call a monomeric reaction that continues to grow. Those particles are free flowing in the blood and they find an anchor point. The anchor points they find are in fact the damaged endothelial layers. When an endothelial layer of the vascular system is damaged via inflammation and the cytokine storm that the spike protein generates, That opens up the natural phospholipid layer of the endothelial layer, and that forms anchor points for these nuclei. From these anchor points, that's when the clots begin to grow. So, I'm trying to encapsulate this in a very simple term. It's quite a complex number. Very

As a doctor, the speaker states they have never seen something so injurious to the human body, invading the brain, heart, and bone marrow. It allegedly stimulates antibodies to attack platelets and other cells, causing unprecedented blood clotting and blood vessel damage. The speaker cites data from the University of Pittsburgh suggesting it causes cancer. They question how a single protein can injure the brain, heart, bone marrow, and immune system, cause blood clotting, and potentially cause cancer, calling it a weapon. The speaker references three papers, including one by Farkas in Military Medicine and Tubei Yan in preprint, which reportedly conclude that it is a bioweapon according to strict military criteria.

Dr. Ana Maria Mihelcia's article states hydrogels are in COVID vaccines and blood clots of vaccinated and unvaccinated individuals. These hydrogels can be programmed, encrypted, and decrypted, serving as a brain-computer interface and fusing humans with machines, referencing MIT research. Mihelcia and Clifford Karnakam found hydrogel plastics (polynes, vinyl, nylon, Kevlar, spider silk proteins), silicone, and sulfur in unvaccinated blood exposed to shedding. This technology hijacks methyl groups needed for detoxification. Hydrogels like polyvinyl alcohol and polycaprolactone are listed as stealth nanoparticles in the Moderna patent. This technology can store memories and visual information, be chemically encrypted/decrypted, and enable secure financial transactions for digital IDs. MIT found success fusing humans with machines using elements found in vaccinated and unvaccinated blood. Professor Sokrat Khizroev discussed using magnetic nanoparticles for brain-machine interfaces, funded by DARPA. Mihelcia's research shows COVID shots alter torsion fields and produce magnetism. Karen Kingston discusses self-assembly nanotechnology, spike protein engineered by electromagnetic frequency, and quantum dots as gene editing. This nanotechnology is in chemtrails, food, water, medications, and vaccines, found in vaccinated and unvaccinated individuals. Protocols to reverse COVID shot effects are ineffective on these hydrogels.

People injected with Graphene oxide may register as a MAC address, acting like an antenna for Bluetooth signals. Some claim spike proteins are moving, but it's actually chips. Avoid putting these substances in your body. To remove Graphene, use humic acid or Chlorella.

There's no such thing as biopsy spreading cancer. They say that out loud, but they have not even one scientific study to show for that, whereas I have 50 to show that they do spread cancer. They just believe so strongly and so blindly what they were told, and they're afraid of the truth because it means that for years and years and years, doctors have been killing people through biopsies. Be very careful. Never do a prostate biopsy. Never do a breast biopsy. There are better ways. You don't need the mammogram with its own radiation. You don't need biopsy to tell you if it's cancer or not. You can be 99% sure just by doing an ultrasound with a technician who knows what she is doing.

I've examined blood samples and have observed anomalies in everyone I've tested, even myself. I'm now seeing things I never saw in un*vaxxed individuals before. I'm noticing unusual formations, like chains potentially building, which typically occurs when the blood is breaking down. These formations seem more noticeable during decomposition. What's interesting is that while the body decomposes, these anomalies don't. They change and morph into something else. The red blood cells are visible, but when these formations mass together, that's when they evolve or morph. It could happen at any moment.

I washed my slides and found anomalies in everyone's blood, including my own. These anomalies resemble liver congestion and may form chains as blood breaks down. They do not decompose like the rest of the body, but instead morph into something else, possibly evolving further. The process of transformation is ongoing and could happen at any moment.

All regulations were violated in the analysis of Graphene oxide. We started with the knowledge that Graphene oxide had been detected and that some individuals exhibited magnetization, which was puzzling. It was crucial to identify the contents to assist those affected. In my research, I utilized a Sigma Aldrich sample of Graphene oxide, confirmed by its certificate of analysis. We observed the particles under an optical microscope to compare them with those found in vials previously analyzed by Dr. Martin Monteverde and Dr. Marcelo Dignani, both of whom reported the presence of particulate material in multiple vials. This material should not be present in injectables, leading us to further investigate the Graphene oxide particles.

Since 2017, I've analyzed blood and noticed unusual findings. Clients often ask what to do about these anomalies, but I don’t have all the answers. My name is Kelly Bacher from Campbellford, Ontario, and I help people identify issues in their blood. Recently, many have sought my services, feeling unwell despite being told they’re fine. I've observed strange, glowing green entities that self-assemble, resembling crab-like or squid-like forms with segmented tentacles. Additionally, there are metallic-looking pieces that seem to degrade into living organisms. When I turn off my microscope, these entities become dormant, but they become active again with heat and light. This behavior is not typical; when blood dies, it should remain dead.

Since 2017, I've analyzed blood samples and recently, I've noticed unusual elements that shouldn't be there. Clients ask me how to address these anomalies, but I don't have all the answers, which is why I'm seeking help. I'm Kelly Bacher, a live blood analyst in Campbellford, Ontario. I help people by analyzing anomalies and suggest meal plans or supplements to improve their well-being. Recently, many people have sought my services, feeling that something is wrong despite being told otherwise. I've observed illuminated, self-assembling structures that resemble crab-like or squid-like organisms with segmented tentacles. I've never seen anything like this before. Additionally, there are metallic-looking pieces that degrade and transform into unknown living things. These organisms become dormant when the microscope is off, but reactivate with heat and light. This isn't normal; dead blood should remain dead.

Here's a shorter version of the transcript: We're examining fluorescent micrographs of plasma from healthy individuals. We're looking at a PPP smear, a smear with added spike protein, and plasma exposed to spike protein. The goal is to see if adding spike protein creates larger microclots than in healthy blood. We'll be conducting an experiment to investigate this. A question was raised about whether blood type matters, specifically if O positive individuals have fewer reactions to COVID. While I'm not certain, it's something to consider.

The presenter describes an independent, grassroots clinical trial that blends Western medical professionals with integrative and holistic practitioners. The trial investigates a new S1 immune subset blood test with markers based on the monocyte white blood cell for the spike protein, a synthetic protein the body doesn’t recognize or readily break down. The team has been able to measure blood tests before and after applying the therapy. They employ multiple testing methods, including an MCG cardiogram to assess cardiovascular effectiveness and an ophthalmologist in Texas who used an OTC scan to measure inflammation in a patient with retinal edema who had vaccine injury and steroid-induced glaucoma after two years of steroid treatment. The before-and-after results showed the retinal edema dropping from around 500 to a normal range of about 200 within eight weeks, which the presenter characterizes as phenomenal and indicative of potential systemic anti-inflammatory effects. When asked how the homeopathic spike detox protocol originated, the presenter explains it as an electronic homeopathic signature coded frequency delivered via a carrier such as sucrose (others use saline or water). The concept hinges on sending programmed signals into the body, which then break down into fructose and glucose and reach every tissue and cell. The goal is to generate a cellular response by signaling frequencies to re-ignite communication within cells, which the team believes is disrupted by long COVID and COVID itself. The protocol includes a diagnostics lab with markers based on white blood cells to enable before-and-after comparisons, and more than 20 practitioners participate in this independent clinical trial. The analogy used is that the signal is carried similarly to how a cell phone receives a signal; cells receive either a disruption or a frequency and can communicate accordingly. Proper frequency alignment could enable the body to heal and repair itself, described as bioelectricity. The protocol is implemented in four systems: cardiovascular, neurological, digestive, and respiratory. Four different protocols are taken once a week because the frequencies persist in the body for about seven days. The interviewer notes the similarity to acupuncture in stimulating the body's natural elimination processes. The presenter emphasizes that Western and alternative medicine professionals are collaborating in a grassroots study, performing diagnostic testing and documenting case reports without grant funding. They acknowledge the ongoing burden of vaccine injury and broader COVID impacts on health. Regarding usage, the therapy is recommended as an eight-dose regimen over eight weeks. For individuals severely ill from vaccine injury or those who have contracted COVID repeatedly, more frequent use may be necessary, while those who have had only occasional exposure might require fewer cycles. Further research is anticipated to elucidate ongoing exposure levels and outcomes.

I recently conducted a survey of embalmers, and 73% of the 269 respondents reported finding white fibrous clots in corpses during 2023. These clots, which consist of fibrin, platelets, and amyloid-like material, are suspected to be a contributing factor in strokes and heart attacks. Embalmers are finding these clots are making it necessary to use multiple injection sites, lengthening the embalming process. While similar clots were observed in 2020, during the initial COVID outbreak, their prevalence exploded with the introduction of vaccines in 2021. The spike protein from the virus and vaccines may be responsible for the formation of these clots. Additionally, embalmers are reporting increases in microclotting and traditional grape jelly clots. One theory suggests "frame shifting," where ribosomes misread the modified RNA code from vaccines, creating aberrant proteins that form amyloid material. I can be contacted at thomashaveland@sbcglobal.net.

I'm Kelly Bacher, a live blood analyst from Campbellford, Ontario. Lately, I've been noticing unusual things in people's blood samples. These anomalies appear as illuminated, green-glowing organisms that self-assemble into crab-like or squid-like shapes with segmented tentacles. There are also metallic-looking pieces that eventually transform into unknown living organisms. When I turn off my microscope, they become dormant, but when I turn it back on, they start moving again. This is not normal because blood is supposed to die when it dies. I don't have answers yet, so I'm reaching out for help.

We can determine if someone has been injected with something by analyzing just one drop of blood. We have found communicative microchips in these vials, with the help of CNRS. These microchips can be seen under a microscope, and a more powerful team confirmed their presence. However, officially, micro technology cannot be used in the medical field without explicit consent. We suspect that there has been a deployment of micro technology, indicating a well-organized organization with limited knowledge. This could explain why no one wants to discuss micro technology, Mac addresses, and graphene.

Okay, let's get started. I need to find the right tools to draw blood, so please be patient. I'll put the scope back on so we can watch. Here are some micrographs: healthy predlopod plasma, then the same plasma with spike protein added. We want to see if adding spike protein directly to healthy blood creates larger microclots than we see in the samples with the spike protein already present. We'll compare the images to see the effects.

I washed my slides and examined blood samples from everyone, including myself. I noticed some anomalies that I hadn't seen in unvaccinated individuals before. These anomalies appear when the blood starts breaking down, particularly during decomposition. Interestingly, while the blood changes, the anomalies do not decompose; instead, they morph into different forms. The red blood cells are present, but when they cluster together, they begin to evolve into something else. This transformation could happen at any moment.

I am a live blood analyst and I have noticed some abnormal things in people's blood recently. I don't have all the answers, so I'm reaching out for help. The blood samples I've examined have unusual illuminated objects that glow green and self-assemble into different organisms like crabs or squids. There are also metallic-looking pieces that eventually turn into unknown living things. These objects become dormant when the microscope is off, but come alive when it's turned back on. This is not normal because blood is supposed to die when it dies.

Biopsies spread cancer, and there are 50 scientific studies to prove it. Doctors have been killing people for years through biopsies, but they blame the cancer instead of the metastasis caused by the biopsy. Therefore, one should never do a prostate or breast biopsy. There are better ways to determine if it's cancer. Mammograms are unnecessary because of their radiation. An ultrasound with a skilled technician can provide 99% certainty.

I washed my slides and found anomalies in everyone's blood, including my own. These anomalies, resembling liver congestion, can potentially form chains as blood breaks down. Despite the body decomposing, the anomalies do not break down but instead morph into something else, possibly evolving further. While observing red blood cells, I noticed these anomalies forming masses that could transform into something new. The transformation process may occur soon or not at all.

Since 2017, I've analyzed blood and noticed unusual findings. Clients often ask what to do about these anomalies, but I don't have the answers. I'm Kelly Bacher from Campbellford, Ontario, a live blood analyst. Many people seek my help because they feel unwell despite being told they're fine. I've observed strange, glowing green entities in blood that self-assemble, resembling crab or squid-like forms with tentacles. Additionally, I've found metallic-looking pieces that seem to degrade into living organisms. When I turn off my microscope, these entities become dormant, but they reactivate with heat and light, moving again. This behavior is not normal; when blood dies, it should remain dead.

The speaker states their transhumanism research team is using an electron microscope to confirm nanotech inside people's blood and tissues. They claim this is a unique capability, as they are the only independent research team with this type of electron microscope, which can identify the compounds of what is being examined. The speaker was shocked to discover that one of the biggest components of the nanotechnology they've been examining is strontium. This allegedly coincides with the known spraying of strontium and barium in chemtrails. They are also reportedly seeing cesium and cesium-137. This allegedly coincides with documentation received from Todd Callender, clarifying that the Department of Energy is the main culprit in creating over 470,000 bioweapons, including Lyme disease and herpes, and selling them on the black market. The speaker claims the Department of Energy uses brewer's yeast to create these bioweapons.

People injected with Graphene oxide could register as MAC addresses, acting like antennas for Bluetooth signals. Claims of spike proteins spreading may actually be signals from injected RFID chips. Even Bluetooth signals from the deceased were picked up. Graphene antennas are mentioned. Avoid putting these substances in your body; use humic acid, shilajit, chlorella, or chlorophyll to remove Graphene.

I am a scientist with expertise in various fields, including quantum mechanics and environmental science. I have analyzed all cause mortality data and concluded that there was no pandemic and no particularly virulent pathogen. The virus does not spread across borders, as evidenced by the absence of excess mortality in some countries. I have also studied global warming and determined that it is not occurring. Moving on to vaccines, my research shows that they are toxic and associated with peaks in all cause mortality. The risk of dying per injection increases with age, doubling every 4 or 5 years. We have observed these patterns in multiple countries. Our work will continue, challenging the establishment scientists who propagate lies and serve the propaganda industry.

The speaker examined a Pfizer BioNTech COVID-19 injection under 100x magnification and observed extreme activity with blinking lights, which they identified as nano and micro robots communicating via light signals. These robots collaborate to self-assemble larger structures identified as microchips emitting a MAC address. The speaker claims to have found 54 undeclared chemical elements, including fluorescent Graphene Oxide, in COVID-19 injections and documented fluorescence in the blood. They state that childhood vaccinations contain the same self-assembling nanotechnology. Analysis of embalmed blood from a vaccinated individual who had been deceased for 8 months revealed similar filaments and micelles filled with blinking lights, exhibiting ongoing self-assembly.