Will Dove 00:07 The COVID injections are causing millions of deaths and potentially hundreds of millions of vaccine related injuries as well as miscarriages beyond anything we've seen before. Scientists around the world are working to understand the mechanisms of injury in the hopes of finding a way to reverse the damage. I have with me today, one of the top researchers in that field, Dr. Stephanie Seneff. Dr. Seneff is a senior research scientist at MIT's Computer Science and Artificial Intelligence Laboratory. She has a Bachelor of Science degree from MIT in biology and a Master's degree and a PhD in electrical engineering and computer science. She has combed through countless scientific papers and identified many of the mechanisms of injury, allowing us to understand on a microscopic level, how the injections were designed to kill and maim their victims. In addition, Dr. Seneff has co authored a number of papers on her findings, along with other eminent scientists and researchers, such as Dr. Peter McCullough. She is here today with a PowerPoint presentation, which will allow us all to understand better what is happening. If you or someone you love has been injured by the vaccines, the information you will see today is an important step toward finding a way to reduce or reverse the damage. Dr. Seneff welcome to the show. Dr. Seneff 01:28 Thank you so much for having me. Will Dove 01:29 My pleasure. If you could please go ahead and share your slides and I may interrupt from time to time with questions as you go through them. Dr. Seneff 01:37 So this is the title of my talk. "Why are COVID Jabs Injuring So Many Globally?" and just start with a illustration, 'they belong in your arms, this does not belong in theirs'. And a quote "all the vaccine mandates should be dropped immediately". We need immediate funding for Vaccine Injury centres, centres of excellence across the United States for screening, detection, diagnosis, prognosis and management. What is at stake here is death. And this is my friend Peter McCullough who has been a fantastic advocate for the injury - Vaccine Injury problem. So here's my outline, germinal centers, vagus nerve neurodegenerative disease - I think that's key to the story. I will talk about sudden death and cardiovascular disease, immune suppression and cancer risk, molecular mimicry and autoimmune disease, and then other concerns reverse transcription and reproductive issues and then a summary. So first of all, germinal centers, vagus nerve neurodegenerative disease, why the mRNA vaccines are more likely to cause damage to the organs than an infection. And this is how I have come to see the situation after many, reading many, many articles about these vaccines. When you get an infection with the virus, it comes in through the nose, it gets into the lungs, it stays in the lungs, as long as you have a healthy immune system because the lung barrier keeps it from getting into the general circulation. If it breaches the lung barrier, gets into the blood, but it still can not get past the blood barrier to get into the tissues. So you've got two barriers that that needs to be breached. Because of a weak immune system, the most important thing to do to keep your health - yourself healthy is to strengthen your immune system so the virus is going to stay contained in the lungs, whereas the vaccine is injected past the lungs past the vascular barrier directly into the deltoid muscle, into the tissues. And this is an important point I believe. Industry is saying oh, it stays in the arm no problem. But that is clearly not true because tracer studies have shown that it goes into the lymph system. It gathers in the lymph node under the arm. swollen lymph nodes are our sign of breast cancer and that's causing swollen lymph nodes. It travels through the lymph system, specially to the spleen, but to other organs like the liver and the ovaries and the testes. So it goes to important places. The vaccine is being carried, the RNA in the vaccine is being carried by the immune cells that have taken it up when they go to the muscle to try to respond to the injury. So the muscles are screaming for help, the immune cells come in. They too, pick up the vaccine and they don't pick up the virus because they don't have the ACE 2 receptor. Immune cells are becoming transfected with the vaccine, and that, of course, causing them to make the spike protein because that's what this vaccine does. The spike protein is extremely toxic. And these immune cells you know, I think of them as sort of animated little beings and they are going to have to make it into the lymph system over to the spleen to tell the B cells and T cells you've got to make antibodies to this stuff. They recognize that there's a problem. They've got a a foreign protein that they're producing, they can't stop making it. If the vaccine RNAs is specially designed to be extremely sturdy. Most RNA lasts for only a few hours. RNA is constantly made by the body but that only lasts for a few hours a vaccine RNA can last for months, two months at least because they found the RNA still present in the lymph node under the arm two months after vaccination, that is extraordinary. And that RNA can keep on making protein over that entire period. Will Dove 04:52 If I may just interject a note there, Dr. Seneff. The reason why we're saying two months is because that's the longest time period of time for which they have tested for it. It couldn't be much longer than that. The reason why these RNA strands are not breaking down, as they should was revealed by Dr. Malone when I interviewed him not long ago. They replaced the Uridine and the RNA with pseudo Uridine, which makes it incredibly stable. And that's why it's not breaking down. They did it on purpose. It is not an accident. It was designed not to break down. Dr. Seneff 05:28 That's absolutely right. And that was a major breakthrough and it may win a Nobel Prize, that particular idea of converting all the Uridine into methyl pseudo Uridine every single one in the vaccine, mRNA sequence is a metal pseudo Uridine, which is not at all natural, which is really, really disturbing. And so I've said all of this. So the exosomes, we have the definitions on the right, thanks to well, exosomes. vesicle, which can carry proteins between cells that can actually carry mRNA between cells as well. In fact, there was a paper that showed that the messenger RNA in these mRNA vaccines can get pushed out inside exosomes, intact, and be traveled to another cell in a distant place. And that cell can take it up and start making the protein that that RNA codes for really quite remarkable. These exosomes know how to protect the RNA from damage, even when it's not all methyl pseudo Uridine. So even normal messenger RNA can survive in these exosomes because they have that lipid particle around them that keeps it safe from the enzymes that would break it down. And then the nanoparticles are actually very similar, as the vaccines are designed to be lipid, to look like lipid nanoparticles that are very similar to LDL particles. That's another kind of particle. You know, the cells communicate with one another through these extracellular particles that they produce and release inside these lipid membranes. And then, I wanted to say here you see this along the vagus nerve in red, that's extremely important. And this is what I believe is happening. In fact, Dr. Mercola, and I were co authors on a paper, innate immune suppression, it talking about innate immune suppression by these vaccines. And a lot of that paper was concerned with this concept of the vaccine, immune cells in the spleen and the spleen is really the center where you make the antibodies. That's where they're pleased to see that these immune cells make their way to the spleen, because that's where you have these germinal centers where the antibodies are produced. So they want the antibodies, that's the goal of the vaccine works very well in terms of producing sky high levels of IgG antibodies, that's a problem that we'll get to later. But also, those cells in the spleen, are furiously making spike protein, they can't stop themselves, they're spilling it out. In those exosomes. Very interesting that exosomes can travel along nerve fibers. And so they're going from the spleen up to the vagus nerve over to the brain over to the heart over to the liver, and causing inflammation wherever they land, it causes an inflammatory response wherever it goes. So you get inflammation in the heart, which is this myocarditis that we're clearly seeing as a signal, especially in young athletic men. This is a paper that showed that, that these vaccines were happily in their, in their view, going to the germinal centers in the spleen. So this is a picture of a germinal center and it's fleeing. And that's where you can get the B cells and T cells, they talk to the B cells and T cells through the exosomes, they actually release the exosomes, which are communicating to the B cells and T cells to say, hey, you need to make antibodies to this, then they can perfect their antibody production to get something very specific to the spike protein. Our data demonstrated remarkable capacity of SARS COV 2 messenger RNA based vaccines to induce robust and prolonged GC reactions. So they like that, because that's how you're going to get those very strong antibody responses. And these epitopes this word epitopes is actually over here defined as an antigen recognized by immune cells. So the whole epitopes are pieces of this protein sequences in the protein that antibodies bind to. And they can actually tell which parts of the protein cause antibody production that are going to match for that particular part of the protein. So this is an interesting, a pilot study that suggested that long haul COVID could be linked to the effects of, of the virus on the vagus nerve. So I like this paper because it's focusing on the vagus nerve with respect to the virus infection. But I think the situation is much worse with respect to the vaccine because of the fact that the vaccine makes its way into the spleen, high concentrations and produces all these exosomes the travel of the vagus nerve. And the paper that that I referred to earlier that Peter and I were both authors on and that's referenced down here that showed from the VAERS database, enormous correlation and we had several different things besides these, but these were the ones that were mentioned in this article: diarrhea, tachycardia, which is heart arrhythmia, dizziness as dysphasia, difficulty swallowing, difficulty Talking, and orthostatic hypotension. All of these things were mentioned above in this article as vagus nerve symptoms. So it seems to be very, very clear. We found over 200,000 events in the VAERS database just for 2021 alone, that showed through adverse reactions that could be related to these various nerves being inflamed and that's what's going on. I think he's you're getting massive inflammation of all these nerve fibers as those exosomes travel along those nerve pathways, and so these are showing here: this is the COVID vaccines, all the cases in 2021 listed as a symptom in the VAERS database. And then this is for all vaccines for 2021. And you can see that nearly all of them are COVID vaccines, this is 97% COVID. And all of these are pretty much 97% COVID 3% of the cases in VAERS for 2021 are all the other vaccines combined together. And here's a definition of the vagus nerve is the main component of the parasympathetic nervous system: controlling mood, immune response, digestion and heart rate very, very important nerve in the body that connects all these organs to one another. Will Dove 10:39 These exosomes can travel along the vagus nerve. Well, the vagus nerve connects just about everything. Dr. Seneff 10:44 Right, and it connects as well. Will Dove 10:47 It's been handed a highway to travel between. Dr. Seneff 10:49 Exactly, it's a backdoor highway, it's outside of the vascular system, which is really important. So you can get to the brain tissues without having to breach the vascular barrier without having to go across the blood brain barrier. A diagram from this paper, which I was nice because it shows the connections. This is the white pulp inside the spleen, this is the splenic nerve. So this hooks up to this celiacs superior mesenteric Plexus ganglion. So these ganglion cell where the nerves hook up to each other, now you've got the vagus nerve traveling to the brain, you can also come to the brain via the spinal column, and people are getting inflammation of the spine of the nerves in the spinal column as well. And that's coming across to this other nerve pathway. So you're getting all kinds of connectivity, passing along that spike protein, as well as the messenger RNA that produces it to all these other cells throughout the body. And this is showing a picture of the vagus nerve and how it hooks up to all these different organs. So they're all going to be compromised, including the small intestine, and they're all picking up spike protein traveling on the vagus nerve, as a consequence of these exosomes. This is a paper that shows that the spike protein activates human microglia in the brain via exosomes loaded with micro RNAs that can influence policy of the cells to change the expression of different proteins. And so there's particular micro RNAs that show up and they these people this was a great paper where they showed that the cells when they are transfected with the messenger RNA vaccine here, they are released by human cells when they're transfected with the virus, with a vaccine. These people showed that microglia would take up those exosomes and then would induce an inflammatory response which can cause injury to the neurons in the brain, central nervous system damage to hyper activation of the microglia, which are the immune cells in the brain. And here we have the definition over here. And transfection is slightly different from infection. You can see here it's a process of deliberately introducing naked or purified nucleic acids into eukaryotic cells, which is the human cells. So this is a paper that shows us that the spike protein has amyloidogenic potential and in this case, where they show that the spike protein binds to heparin and to heparin sulfate, there are a variety of proteins that can misfold these amyloid proteins down here, this definition, they're produced naturally but they can misfold under certain conditions, and when they misfold, they cause things like the plaque the amyloid the amyloid plaque that's famously associated with Alzheimer's disease. The spike protein binds to this heparin. heparin is a is a fascinating molecule most highly sulfated molecule in the body. Lots of sulfate negatively charged, which means that it tracks these proteins, they bind to the heparin and heparin binding sort of gathers them together to increase the concentration and to increase their likelihood of this multiple proteins stuck together in a larger unit. Those are the form that then eventually become the fibrils that produce the plaque in Alzheimer's. And there's many different proteins that can misfold. And they're specifically associated with all of these nasty neurological diseases are connected to misfolding of these particular proteins. Okay, sudden death and cardiovascular disease, very important paper that's just come out with a actually did an autopsy of five patients who had died unexpectedly very shortly after the COVID-19 vaccine. This is a very critical thing that we need to be doing more of to actually do autopsy to see what's happened in the heart when people unexpectedly just dropped dead. We're seeing too many people doing that these days. We need to understand what is going on there. These people proposed and I agree with this, that molecular mimicry is playing an important role. There's other papers that have shown that the spike protein itself has many sequences within it, that are similar to sequences in many human proteins that are associated with many different autoimmune diseases to show the mRNA vaccine causing these immune cells to get to congregate in the heart and they show they looked at the immune cells and found them present to these photographic mechanisms. They can see all these macrophages invading the heart that's not good because that's going to cause inflammation, and then finally causing like a heart attack. It's when two molecules have very similar sequences so that the immune system may see proteins natural to the body as if they are an invader. They learn to recognize the spike protein and you could say they're near sighted, they're not quite, they don't have a perfect match, but it's good enough, they go ahead and bind, they cause trouble. And this is a well known phenomenon that's been strongly linked to various autoimmune diseases. Will Dove 15:11 There's, there's an autoimmune response happening. And that causes inflammation. Now, acute inflammation isn't a bad thing, that's your body healing itself, but chronic inflammation can eventually lead to a loss of function within certain cells, the cell stops working. And that's what causes the damage eventually. And so if the heart has these proteins in it that are very, very similar to the spike proteins. So that molecular mimicry is causing the immune system to attack the heart muscle. Dr. Seneff 15:44 That's right. Will Dove 15:45 With it causing that chronic inflammation. That virus -- Dr. Seneff 15:48 - is slowly killing the heart. And then at some point, it just can't function anymore, and you die. So you're, you're getting worse and worse and worse. And then finally, it goes over the edge. Will Dove 15:56 And younger people, sometimes we see them dying very, very shortly after, and sometimes older people too. But I was interviewing Dr. Jessica Rose yesterday on the VAERS data, and she was showing where the - after the first and second shot. Yes, we're seeing a lot of younger people dying or getting myocarditis at the very least. But the third shot was causing myocarditis in a much broader age range and not hitting these younger people. What if these proteins in the heart muscle that are being accessed by molecular mimicry exists in higher concentrations in young people, and then drop off as they get older. And that would explain why you need to have more and more shots before it starts causing myocarditis, in the older population? Dr. Seneff 16:44 It does seem to me like athletes are especially susceptible, I don't know if that's just because I hear about all these athletes that are dying, but it feels like young, athletic men. And you may be right that they just have more of whatever this protein is. When you exercise a lot, your heart gets bigger, and gets stronger and has more of you know, and so maybe there's just more of this protein that is matching that the spike protein and so they're more likely to be injured more quickly. So this is a paper that just came out 'increased emergency cardiovascular events among under 40 population, Israel during vaccine rollout and the third COVID-19 wave. Bottom line is 26% increase in cardiac events among men aged 16 to 39. Compared to the previous year, we have here the vaccine. So this is the when the vaccine was delivered over time, this is October 2020. And then over here is 2021, May 2021. So there's over a period of time, and they were pushing massively that vaccinating here, on the first vaccine. And then this one is the second vaccine. And this red curve is the important one, which is cardiac arrest. They were looking at emergency calls for cardiac arrest. That's the data that we're getting. It's a large population in Israel. And you can see this wave coming up here reflecting this first vaccine section, second vaccine series, causing this rapid increase in cardiac arrest. It came down and then it came back up again over here and that - he thinks this is the paper, they suggest that this is because this of this green one here, which is people who had a previous infection at first, they were saying they weren't sure what to do with them. And they finally said yes, they should get a vaccine. So this started happening that these people who had already been infected, and that's dangerous, because they already have antibodies. And this is due to the antibodies overreacting. So once you've already got the antibodies, you can get into bigger trouble with the second shot. This is essentially a second shot because it's after the infection. Will Dove 18:37 So what I have to ask, though, because it's going to be very important to the interpretation of that red line, the calls - emergency calls for heart attacks, is the third, fourth shot, not on this chart. Dr. Seneff 18:50 Good point, it doesn't look like it is and probably these people over here are getting a booster shot along in here, right? They're getting a booster shot. So that may also contribute to this signal here. It might not just be this one, but also a booster shot which is not shown on here. That's a good point. Will Dove 19:05 And the reason why I asked because you've marked it very well. You've marked March 7 there, you can see the line folks, second vaccine, they start dropping off dramatically, the injections and immediately the calls for cardiac arrest start to drop off. But when we look at that green line, yeah, well it starts going up but it keeps going up. So my suspicion is that what we're seeing here is third, fourth, fifth shots. It's likely what's driving that big spike there. Dr. Seneff 19:35 So this was a single person, this 76 year old man with Parkinson's disease and he actually his Parkinson's got worse after he was getting his vaccines, probably didn't think the vaccines were causing that. He got this multifocal necrotizing encephalitis, which is a very nasty necrotizing means the tissue is actually dying. And encephalitis is swelling in the brain. And then he also had myocarditis at the same time so both the brain and the heart were affected after this vaccine, and this was his third vaccination, so he had already had two. The third one - and everyone gets worse than the one before. And then the what they said here, surprisingly, only spike protein, but no nucleocapsid protein could be detected within the post I have information - in both the brain and the heart. So the nucleocapsid protein is another protein that's in the membrane of the virus, but it's not present in the vaccine. So if it's only spike protein, it really points to being vaccine related. And in fact, he had no record of having had COVID-19. And actually, I think the presence of the nucleocapsid protein probably changes greatly the behavior of the spike protein. So I have wondered about that, because the vaccine has only spike protein, which is displayed on the external surface of the exosomes with no nucleocapsid protein, whereas the virus may be hiding certain parts of the spike protein to the nucleocapsid protein that could be protecting you from the worst aspects of what the spike protein can do. I don't know if that makes sense. But I suspect I've wondered about that, with only spike protein and no nucleocapsid. I think that's problematic. Will Dove 21:01 People who have been infected with COVID 19 may have greater resistance to the damage from the injections? Dr. Seneff 21:08 Well, I'm thinking that when that the virus itself is not as dangerous as a spike protein alone, but the ones that could be more likely to cause molecular mimicry might be hiding inside the nucleocapsid protein such that they're not available to the immune system. So you don't develop those antibodies that you otherwise develop when the spike protein is exposed, all by itself without the capsid protein able to hide it. So you'll get the antibodies to parts of the spike protein that would be very dangerous in terms of molecular mimicry, causing things like inflammation in the heart. And this is a nice photograph here of the brown material. That's the spike protein inside the capillary and heart. So this is very clearly showing that the spike protein is there inside the heart of this patient. So this was a quote in the paper since nucleocapsid poaching of SARS COV 2 was consistently absent, it must be assumed that the presence of spike protein in the affected tissues was not due to an infection, but rather to the transfection of the tissues by the gene based COVID-19 vaccines. This is a very strong statement in the paper, which I certainly agree with. And especially because it was no evidence that this person had had the disease. Well, this was an exciting paper for me, PD-L1 over expression following COVID vaccination. And I will admit, I didn't know what PD-L1 was when I saw this, but it certainly looks dramatic. And I wanted to know more about this particular protein, which is - has an odd name: Programmed Death Ligand One, it actually binds with this PD-1, the two of them bind together, so receptor on the immune cells a response to signal displayed on a sick cell. And this dramatically increased in the granulocytes and the monocytes in response to the vaccine. And this was done two days after the second vaccine, 62 patients. So that's quite a bit of data. And you can see this is the range for the patients. And this is the normal controls a very, very low expression of this protein. So this is a protein that is a marker for certain disease states. And what they were proposing in the paper was that the immune system was over activated, cells needed to express this protein as an immunosuppressive effect. So this goes with the paper that McCullough and I wrote, 'Innate Immune Suppression by the Vaccines' that we saw evidence of and we describe in that paper. The immune system is so strong in this reaction that it needs to be tamed, it needs to be turned down. And here we have this nonspecific, immune suppressed suppressive effect, which is the immune system is suppressed, not just against COVID, but against everything, including cancer. And that's an important point because you suppress it against cancer that allows cancer to express. So when you have already cancer in remission, it could come back out again. This paper says that PDL-1, PD-1 signaling pathway, that's the cancer cell expressing PD-1 PDL-1 binding that can actually inhibit the activation of these immune cells and enhance the immune tolerance of tumor cells. And so we have something called tumor immune escape in which the tumor develops resistance to the carcinogenic to the drug that you're taking that's trying to kill the tumor. So you take some kind of an anti tumor drug, but the tumor learns how to not be bothered by that, because of this PDL-1 signaling, it just shuts down the immune system such that it can't remove that cancer cell and it can keep on living. And then here's a paper talking about antibodies to PDL-1 and to PD-1 to treat cancer. So there's a lot of research going on with the idea of providing antibodies to the patient, that would reduce the expression of these proteins. So to reduce the expression of PDL-1 in order to fight cancer, which means that the increased expression of PDL-1 is going to increase the risk of cancer so that the corollary of that Will Dove 24:35 This PD proteins, what they do is they're a response to chronic inflammation, that immune response that's out of control, and it's the body saying slow it down, because it's going to prevent the killer T cells from recognizing infected cells and attacking them which has the effect of damping down the immune response. But the problem is it now it's not responded to cancer, the CDH cells that are the primary line of defense against them. And if you were say, to do this to somebody who was suffering from these injections, and get those levels back up, well, the problem is now you're going to really increase the autoimmune response. And that itself could kill them. Dr. Seneff 25:17 Yeah, I want to say that this definition is probably not quite right, because I think it's actually killing off the immune cells to this program. So they have a very odd name. And I was trying to figure out exactly why they have that name. It - they're the opposite of allowing the cancer cells to die, they're allowing the immune cells to die. There's a here it shows down regulation of T cell activity. So the T cells, I think, are being turned off by this signaling between these two here. So it's suppressing the immune cell response to the tumor such that the tumor can live. It's horrible to hear about all these things that these vaccines are doing, but they're definitely expanding my knowledge of biology. And I always love to learn more biology, and especially when I'm motivated, because it's something that's telling me, I need to know more about this. And it helps me to remember what I'm reading because of this connection to something like these vaccines, you know, becomes more important to me to know this. So molecular mimicry and autoimmune disease. This is the talk paper I was talking about earlier. And I thought I had this slide here. It's quite astonishing. This particular paper, potential antigenic cross reactivity between SARS COV 2 and human tissue with a possible link to an increase in autoimmune diseases. The nucleocapsid protein and the spike protein and some other proteins. But this is specifically just a spike protein from that paper, incredible the number of different proteins that are really important in human biology over here on the left that have segments in them that are similar to segments in the spike protein. And these proteins, when they do have antibodies to these proteins, they're linked to all these different diseases. So here celiac disease, scleroderma, lupus, multiple sclerosis, autism, primary biliary cirrhosis, hepatitis, myocarditis, Sjogren’s, mixed connective tissue disease, and these are various kinds of heart problems. And all of these diseases are associated with antibodies to these proteins, which are have these pieces that are similar to the spike protein. So the spike antibodies could potentially cause any of these diseases, which is really shocking. Will Dove 27:09 This, this all has to do with the mimicry that you were discussing earlier, that what's happening is that the suppose vaccines, they're seeing these proteins that look very, very similar to the proteins that they're set up to attack. And so they're attacking those proteins and causing all these problems. Dr. Seneff 27:26 Right. And I want to point out, by the way that vaccines are have a skewed antibody response, they produce sky, high levels of IgG. There's different names for the different kinds of antibodies, just IgM, which is mucosal, and those are typically like in the lungs, when you get the infection and mucosal antibodies, and the IgG antibodies are in the blood. And when you have a skewed imbalance between those two, too much IgG and too little IgM, the IgG are more likely to cause autoimmune disease, this is something that I found a paper on. So I think that vaccines are the cause of that skewed response are much more likely to cause autoimmune disease than the antibodies that are produced from the disease. So this was a autobody study on nine patients who died from COVID 19, the disease, they have this picture, this graph from the table, a nice illustration of what's happening, it's complicated, you don't get this complement cascade activation, which triggers blood clots and things like that, and also injures the endothelial wall, right, here's an injury. And then you go on to get this endothelial cell damage, which activates the platelets, and the platelets aggregate, now you're really building up the blood clots, but you're also opening up the barrier, so that things can get in. And now you have things coming in including immune cells, this is the lymphocyte, moving past the barrier into the tissues of the brain. And then that causes the microglia to get activated. And once they're activated, that's how you get that inflammation, the neurons end up dying because of the inflammation that's caused by the microglia that are responding to the invasion of these immune cells - monocytes coming in, macrophages that are going to, and the fibrinogen, which is going to also irritate those. These microglia respond to all of these things by becoming activated and causing inflammation. And then I love this, the paper said one possibility is that anti-Idiotypic antibodies against the spike protein might bind to the ACE2 receptor on endothelial cells triggering the cascade. I love this sentence. And I didn't know again what anti-Idiotypic antibodies were. And I can see he's got a lovely definition down here. You have this spike protein, you get these IgG antibodies to the spike protein - sky high levels, and that probably causes them to also be immunogenic. And so they cause antibodies to them. So you get antibodies, back again, from the antibodies that actually look a lot like the spike protein. So you're actually kind of reproducing a mirror image of the spike protein in those second level antibodies that can then behave like the spike protein and attach these to ACE2 receptor that is super, super wild. And I learned about that in the papers that I read. So it causes an amplification of the autoimmune response, but it can cause the antibody to look like the original thing that caused the whole cascade. Really, really amazing that the antibody can behave like this spike protein also bind to these receptors and then cause all of a certain things the spike protein would cause. Will Dove 30:11 That slide, that is from people who were affected with COVID-19. And the spike protein expression from the injections is vastly greater than it is as the infection. So what would be seeing there among the injected would be amplified many times over. Dr. Seneff 30:27 That's correct. Will Dove 30:28 So in effect, it's a manufactured kind of Alzheimer's, Dr. Seneff 30:33 I would say. So I would say exactly that, yes, a very direct path to Alzheimer's. And I predict that we're going to see an alarming rise in Alzheimer's in the future and younger and younger ages, people are going to develop Will Dove 30:44 Perhaps it's a very impolitic way of saying this but I think it's also a very blunt and honest way of saying it. These injections are making people stupid. Dr. Seneff 30:54 I would say so. I would absolutely say so. Yes. And of course also, because they traveled much more easily along the vagus nerve to get to the brain from the vaccine than from the disease, you have to breach all those barriers to get there from the disease. Possible role for anti-idiotypic antibodies in SARS COV 2 infection and vaccination. So this paper is bringing in the vaccination as possibility too This is where you see this spike protein being displayed on the surface, the antibodies getting induced, this is the AB-1 antibodies, they're going to bind to spike protein, but then those guys can produce antibodies to them. So now you've got a second AB-2. So AB-1 is the original one matching spike, this one matches the part that matches the spike back again. So this becomes like the spike protein. And now this one can go over here and hook on to the ACE2 receptor just like the spike protein does. So if it's an antibody to the place where the ACE2 receptor is, you can bring back the spike protein at that, that ACE2 receptor binding problem with a spike protein through the antibody. Will Dove 31:52 The end result of this is going to be an amplification of that autoimmune response. Dr. Seneff 31:56 That could be the explanation for these strange cases in which they don't see any evidence of the spike getting into the brain, yet you have that obvious inflammation going on there. Will Dove 32:05 And because the body recognizes the spike protein as a toxic substance. Dr. Seneff 32:10 Right. Will Dove 32:10 These guys are going to have the same reaction there. The body is going to have that autoimmune chronic inflammation response, because it's a toxic substance. Dr. Seneff 32:19 Right. And that's the thing, I think this chronic inflammation is really a problem. Usually, as you said, you know, inflammation is part of healing. But if you can't heal, you keep on getting the same irritant, you can't clear it. Other concerns reverse transcription and reproductive issues, RNA back to DNA, that's the reverse transcription, you have this definition here, the process of an RNA molecule creating DNA capable of reproducing the original RNA. So once you convert it back to DNA, now you've got a permanent version of it, because the DNA can clone itself to make more DNA. And the DNA can go to RNA back to protein again, so you've got a sort of stored memory of that RNA molecule that's permanent, that can potentially be permanent. And so they show that cells, they really for cancer cells, they grew them in culture, they expose them, they essentially gave them this the mRNA vaccine, they took up the RNA, and they had converted into DNA after only six hours. Six hours later, there was DNA, coding for that same RNA molecule very fast. It was really quite amazing to me that it happens so quickly. And then you need to get that DNA integrated to the genome to actually have it be a permanent part of the human genome. And it can be passed down to your to the future generations. But it may just stay inside these plasmids, you know, that can contain the DNA that can - and those plasmids are outside of the original of the genome itself. They are autonomous, but they too, can clone themselves. And they can make RNA, they can do everything that the chromosomes can do as far as preserving an ability to keep on making spike protein forever. And so this is a picture of the exposed cells versus control to show all this lighting up is indicated indication that it had worked. This is from 2006. So it's long before COVID, right, but they're talking about sperm. And they show that sperm also have this reverse transcriptase line one expression. Sperm and the cancer cells both express line one, and they can reverse transcribe exogenous RNA molecules. And there's a nice definition over here originating externally such as the vaccine, that's exactly what the vaccine is, an exogenous RNA molecule. And they can make these so-called cDNA copies, which are actually a circular DNA, all the sperm not just the one that fertilizes the egg, are releasing plasmids, and the plasmids are picked up by the fertilized egg. And then they can be maintained in that person for the rest of their life, and they can be passed on to the future generations. That's how you can get external RNA molecules preserved for future generations. And so this could be happening with the vaccines as well. Will Dove 34:50 As I was studying this, something hit me and I want you to once again, verify that I'm getting this right because we've heard a lot of talk about this reverse transcriptase. rewriting our DNA. But if I'm understanding this correctly, that's not exactly what's happening. It's not rewriting our chromosomal DNA that's staying the same. What it's doing is it's creating these plasmids that are actually kind of they're almost like stowaways, along with your genetic code, and they can be delivered by the sperm, but they're separate from the chromosomal DNA. And if that is correct, then if we can find a way to remove those plasmids, we stop it from passing from one person to the next. Dr. Seneff 35:31 Right. But I think that's extremely difficult to do. These plasmids are really I think they probably are part of the whole evolutionary process. And I think that at some point, the plasmids can get integrated into the human DNA and become part of the genome. And that's probably how the genome evolves, you know, we see actually, pieces in the human genome, that are viruses, viruses that God inserted into the human genome from long ago. Those proteins are preserved, borrowed from the viruses. So I think viruses are a very important part of evolution. And the whole evolutionary process relies on viruses. So it's really quite wild to think about how we adapt to our environment over time reflecting toxicity that we're exposed to whatever kind of stressors we have, you know, if it gets too hot, I mean, all these different stressors that occur in life result in changes, and those changes can be facilitated, and maybe accelerated through the mechanisms of viruses, I actually think that may be one of the important roles that viruses play -- Will Dove 36:37 -- But the important thing that I wanted people to take away from this was, it's not rewriting your chromosomal DNA. Not yet anyway, it might in time with enough generations. But for right now, it's not. You're still a human, you're still homosapiens, it didn't change. But it is acting as a stowaway on your genetic code with these plasmids. And it's carrying that thing along that DNA that can replicate and be passed from you to your children. Dr. Seneff 37:07 We could not guarantee that it was actually in the genome, but it was definitely there. So this whole issue of integrating into the genome have to be careful not to say that's been demonstrated, these people only demonstrated that it can be converted to DNA, which is the first step, but they did not demonstrate that it can be integrated into the genome, but you don't need it to be integrated in order to have a problem. This one really surprised me too. I was quite shocked by this, I have to say, and this is these IgG antibodies, I talked to you about how the IgM antibodies are deficient in response to the vaccine. And when you have a high IgG, and a low IgM, IgG antibodies can become more problematic without the IgM. And that's what you're getting with these vaccines. They took this particular, it has this name, that antibody, which was one of the neutralizing antibodies that was produced in response to the spike protein, human antibody produced from the spike. And then they injected that antibody into the peritoneum and you've got the organ cavities that's around the gut, in the outside of the gut, but around it in the external area. Will Dove 38:06 So I realized my definition of peritoneum there is not strictly correct, but in this sense, I think that's what they meant. Dr. Seneff 38:11 I think the organ cavity is a good way to say it. I like that as these rats were pregnant. So they picked up this this antibody center, probably onto the influencing the fetus, that the multiple fetuses that were in there, and so the offspring of the pregnancy were highly damaged with - they had kidney injury, heart damage, inflammation in the brain and when they were born dead. I mean, it's really, really surprising what happened to these pups, due to the exposure of their mom to the antibodies that are produced by the humans in response to the spike protein found broadly to human inflammatory tissues. And they predicted it would increase the severity of pre existing disease, both cancer and various inflammatory diseases like lupus and multiple sclerosis. There have been a lot of people who've been looking at birth rates, and you're probably aware of that. And various countries are finding data from countries that do a good job of tracking that. And this is data from Switzerland, which are really quite striking. This is nine months here. So you can see this echo, this is all the vaccines going on. And the echo of the vaccines is the sudden drop. The number of live births went way down in this period, as an echo of the increase in the number of vaccines quite striking. To me, very, very strong evidence, I think of issues. The ovaries were the second highest contamination of the vaccine, of all the organs the spleen had the highest levels, and the ovaries in the females had the next highest level of RNA from the vaccine. And so they showed average decline of -10%, which is the strongest birth rate declined in over 100 years for Switzerland. So that's another thing to be watching. We're gonna get more and more data of course, as time passes, and eventually it'll become clearer, but I think we're gonna find it a major problem with reproduction as a consequence of this massive vaccination campaign. So in summary, mRNA SARS COV 2 vaccines are based on the poorly evaluated technology with potential to cause many debilitating diseases. Immune cells carry the RNA to the spleen and they produce massive amounts of toxic spike protein releasing it into exosomes, the exosomes traveled to the brain to cause neurodegenerative disease. They travel to the heart to cause cardiovascular disease. The vaccines, upregulate, PDL-1 and immune cells leading to immune suppression and impaired clearance of tumor cells. The vaccines induced high titers of antibodies. The spike can cause autoimmune disease by molecular mimicry. Evidence is growing to suggest infertility issues and the potential for the RNA and vaccines to become integrated into the human genome with unknown consequences Will Dove 40:34 I am going to take just one moment to, I'm going to share my own screen folks split it over nine months was struck to see, you can see much more clearly, the correlation is not a perfect correlation. But then we need to take into account the fact that with these bars here, that's the total number of vaccinations. We don't know what percentage in each month were women, if we could get the figures for pregnant women and just them, I suspect, we would see an even stronger correlation. Dr. Seneff 41:04 And there could be a delay to I mean, certainly if you get vaccinated before you get pregnant, and then it could cause trouble getting pregnant. Will Dove 41:10 And the globalists who designed it, they have two objectives. One is depopulation, and the second is control. And when I look at this, and especially in the context of the information you provided, it seems to me to be a perfectly designed bio weapon to do exactly that. It's sterilizing people, it's killing people, it's crippling people. And then that's a big factor is that if you can make people into patients, then you have to use up resources to look after those people while they're not contributing. And this is the thing that really bugs me most of all, is as we were discussing, it's basically causing Alzheimer's. It's making people stupid, well, how much easier is going to be to control them because they can no longer think clearly. And brain fog and I happen to know this is that the number one side effect that's reported by people who've been injected, and I'm not putting words in your mouth, this is me. I can't not draw that conclusion. It was designed to do that. They knew it would do that. Dr. Seneff 42:06 And I do have very little doubt that it did come out of the lab rather than natural infection. I think the evidence is overwhelming. Will Dove 42:13 Oh yeah. absolutely. Dr. Seneff 42:14 It came out of a lab in Wuhan. Well, whether that was an intentional release, or unintentional release is a big question. Will Dove 42:21 There are two sequences of proteins on the spike in the original virus that are identical to sequences of proteins and a patent that was filed by Moderna. In 2014. The odds of that happening by chance are one in 72 million. Dr. Seneff 42:37 Wow. Will Dove 42:38 So they've been working on this for a long time. And it wasn't, you know, the Chinese might have finished it. They didn't start it, Dr. Seneff 42:45 Or whether they knew because it was a plan that they wanted to actually carry out, I don't know. I mean, that's all going to be very hard to figure out. Will Dove 42:52 I think the explanation how they can do what they do is that they are psychopaths and they have no conscience, Dr. Seneff 42:56 I think there has to be, I mean, that's an easy word to use to just justify it. But it doesn't make it any easier to accept. Will Dove 43:04 It makes it very difficult for any of us with a conscious to accept to wrap our minds around how anyone could be that evil, could have no conscious not care what kind of damage they're causing. But when we look at the evidence, we see, you know, Event 201, which happened a month before they announced COVID-19. And then there was another one also run by Gates and company that was done just about a month or two before monkey pox was announced. And now worryingly, a couple of months ago, Bill Gates and company did another exercise called SARS 2025. Dr. Seneff 43:40 I saw that too. I saw the write up about that. It's all coincidence, I'm sure, right? Will Dove 43:46 Oh, yes. Yes, I'm sure it is. It's all coincidence. All right. Dr. Seneff, thank you so much for taking the time to compile all of this information and to share your knowledge with our audience.