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Scientists just figured out how to reverse aging using AI. And this is a massive breakthrough. We can now reprogram any human cell back to age 20. Heart cells, brain cells, skin cells, all reset to their biological prime. And here’s the wildest part…the technology to do this, has...

68,643 görüntüleme • 7 ay önce •via X (Twitter)

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New Research Deep Dive: The "Shedding" Conversation Just Got More Serious A new in-vitro study (using human cells in a lab) on the Pfizer mRNA vaccine has revealed critical findings that can no longer be ignored. Let's break it down. The researchers confirmed two major things: 1️⃣ Spike Protein Production: The cells successfully took up the mRNA and began producing the SARS-CoV-2 spike protein, displaying it on their surface. This was expected. 2️⃣ Spike Protein "Shedding" via Exosomes: Here's the crucial part. The cells didn't just keep the spike protein to themselves. They packaged it into exosomes—tiny extracellular vesicles cells use to communicate—and excreted them into the environment. Why does this matter? This provides a potential mechanistic blueprint for how spike protein could travel systemically throughout the body after vaccination. These spike-laden exosomes can enter the bloodstream and, theoretically, deliver their cargo to distant organs and other cells. But the most alarming part? The authors note a profound lack of safety data. They explicitly state: We have no scientific studies to determine if this exosome-mediated spread of spike protein is toxic to other human cells. Even more concerning, they observed "pathological changes" and toxicity within the cells producing the spike. And these weren't weak cells—they were robust, immortalized embryonic kidney cells, chosen for their resilience. If these cells showed adverse effects, what is the impact on our more delicate primary cells? The authors themselves caution that proper toxicology studies on normal human cell lines are urgently needed... and are currently unavailable. This isn't conspiracy theory. This is cell biology. The conversation must evolve from if spike protein can travel, to what are the systemic consequences when it does. The call for rigorous, independent safety science has never been louder.

Camus

48,219 görüntüleme • 6 ay önce

🚨Here's what a lot of people misunderstand about cancer treatment, says drpaulmarik: "Cancer is not homogeneous. The somatic mutation theory—which is the current theory in which treatment is based—posits that you have a mutation in a single cell, and that gives rise to a whole population of cells that look the same and have the same mutation. But the Cancer Genome Atlas has shown that that theory is completely wrong. The cancer cells are very heterogeneous, so they're made up of very different populations of cells with different mutations, and one of the populations is the cancer stem cell. It's a sub-population of the cancer. These are generally slow-growing, but they're distinct in that they have the ability to divide indefinitely and grow indefinitely, and can change their characteristics. Basically, if you get rid of the fast-dividing cells, which is the cancer, you're left with the stem cells, which then become the roots, which grow back to form the tumor" sometimes years later. Conventional chemotherapy gets rid of the fast-dividing regular cancer cells but *NOT* the stem cells. So the key question is: how do you get rid of the stem cells? “There are a number of repurposed drugs that do it, and this has been well-established in scientific medical literature. One of the most effective treatments to knock out the stem cell is the famous horse deworming medicine," says drpaulmarik. Yes, ivermectin. Independent Medical Alliance

Jan Jekielek

96,002 görüntüleme • 1 yıl önce

Great explanation by Bret Weinstein: "The mRNA platform solves a problem. It is a gene therapy technology, and it allows you to deliver an mRNA message. mRNA means messenger RNA. Usually messenger RNA is produced in the nucleus of your cells. It moves to the cytoplasm, and then something called a ribosome translates it into protein." "Protein does the work of the cell. It creates most of the structures of the cell. So what they innovated was a mechanism for getting RNA messages that they controlled, that they dictated into cells so that your cells would produce a vaccine-like substance. So instead of a vaccine factory, they had a factory that produces a injectable that turns your cell into a factory." "I mean, it's a brilliant idea at one level Not ready to be injected into a human being and frankly There is a fundamental flaw in it that cannot be solved with present technology. This is where the rubber meets the road. When you get sick with a virus, that virus hijacks your cells. Your cells are covered in protein that you yourself produce." "By a complex process in utero, your immune system learns to ignore every protein that you yourself make. So the way immunity works is you learn to ignore your own proteins and then anytime you see something that you don't recognize. You fight it as a pathogen. When a virus invades your cells it hijacks them and they produce more virus. They do that they produce proteins that your immune system does not recognize." "So your immune system has a capacity to surveil all your cells and when it encounters a cell that is putting out proteins that you yourself make but also proteins. It doesn't recognize it regards those cells as virally infected and it destroys them because no matter how important the cell in question is right? There's no way to get the virus out of it. So killing it is a better plan than leaving it in place." "So now these folks who made the mRNA vaccines inject them into people and they tell us that the vaccine will stay in the deltoid. Well, no, it's not going to stay in the deltoid. You're injecting a fluid into a space that doesn't have room for it's going to leak out and in many cases, the needle itself will just by accident have landed in a vein and that injection will actually go in a concentrated way into the bloodstream." "There is no targeting mechanism at all on the lipid nanoparticles the fats that are used to transport these mRNA messages into the body. You may remember from chemistry that like dissolves like. Fats are what these mRNAs are coated in every cell in your body has a fat layer on the outside. Those fats join the mRNA message goes into the cell the cell starts producing this foreign protein your immune system Sees that foreign protein." "This is actually part of the design. Your immune system is supposed to see it That's where the immunity is supposed to come from But your immune system in recognizing these foreign proteins on your own cells will assume they are virally infected and it will destroy them." "If that happens in your deltoid, not a huge deal. If it happens in your liver, probably not a huge deal if it happens in your heart It's a huge deal, especially if you've got a big concentrated glob of it. So a bunch of cells in your heart were producing these foreign proteins and got attacked by your immune system because your heart, a is very well protected." "So it doesn't usually suffer from insults. B it has very low capacity for repair. In fact, mostly it doesn't repair it's scars. Hmm. So if you've got a concentrated dose of this in your heart a bunch of your heart cells got transfected. Your immune system will kill those cells that leaves you with a wound." "It's a wound you don't even know you have because your heart is not innervated for you to be able to feel that damage. There's no benefit to it because such damage would be very unusual so you've got a damaged heart. It's never gonna be the same." "At best months will pass and it will scar over but at worst maybe you're on the soccer field and you're going to score the big goal and your blood pressure goes up to a level that hasn't been in months and that wound does arbitrary things. Maybe you collapse. So the key the punchline to this story is none of those things have anything to do with the content of the message that was encoded into these things." "That just has to do with the platform. The platform has this defect built into it, and anything, any disease you attempted to remedy with this mechanism would cause the same problem. So that's a dire failure. I would also point out, there are many other flaws with this technology. The way the mRNA molecules were stabilized was irresponsible." "It made for a process that cannot be terminated and is not naturally terminated by biological biological pathways. It also caused the ribosomes to incorrectly translate into protein so that you get arbitrary products that have arbitrary consequences. The manufacturing of these injectables was piss poor the quality control was garbage." "There are all kinds of impurities contaminants including DNA from SV40 which has potentially cancer inducing properties so these shots were an absolute horror show design failure after design failure manufacturing flaw after manufacturing flaw and the idea that anybody injected healthy people with them is needs to be explained."

Camus

607,223 görüntüleme • 1 yıl önce

Joe Rogan and NFL legend Terry Bradshaw get into a serious debate over stem cells. Bradshaw argues stem cells “don’t work” because people go back for them “again and again.” Then Rogan fires back that he healed his fully torn rotator cuff in just 6 months using stem cells, and it sounds so insane to Bradshaw that he can barely believe it. BRADSHAW: “I got a bad hip right now. I’m telling you, Joe, it’s killing me. And I got it injected.” ROGAN: “With stem cells?” BRADSHAW: “No, no, I don’t do stem cells.” ROGAN: “Why not?” BRADSHAW: “I don’t believe in stem cells.” ROGAN: “You don’t believe in them?” BRADSHAW: “No. I [know] too many people… They went back and did it again [and again].” ROGAN: “Why’d they keep going back?” BRADSHAW: “Because it didn’t work.” ROGAN: “What’s wrong with them?” BRADSHAW: “Mostly knees and ankles.” ROGAN: “Okay, so you’re probably talking about arthritis, probably talking about degenerative knee conditions, ankle conditions. So the amount of damage that you’re trying to repair with stem cells, you’re going to get a little bit of benefit in something like that if it’s that far gone. But stem cells work.” BRADSHAW: “You do stem cells?” ROGAN: “100%.” BRADSHAW: “What hurts?” ROGAN: “I had a rotator cuff tear that completely went away.” BRADSHAW: “Now, that’s at least a year.” ROGAN: “That’s what you say.” BRADSHAW: “At least a year.” ROGAN: “I had a full-length rotator cuff tear. I got stem cells shot into it.” BRADSHAW: “A full tear?” ROGAN: “Full tear. My doctor told me I 100% was going to need surgery… [Instead], I get this stem cell treatment in Vegas. Dr. Roddy McGee hooks me up with the stem cell treatment. And then six months later, he gives me an MRI and he says, ‘The rotator cuff tear is completely gone.’ Literally, the tear doesn’t exist anymore.” [Bradshaw’s skepticism starts to fade]

The Vigilant Fox 🦊

1,029,588 görüntüleme • 7 gün önce

Ok so treatment has begun here at Auragens. First day I’m getting stem cells via IV, these cells are from an umbilical chord, so basically Day One cells that haven’t been programmed yet, is how it was explained to me and the wild thing is the cells know where to go in your body to attack inflammation and injuries. Wifey getting stem cell facials and IVs for anti-aging. I am also having exosomes in a nebulizer for brain health. GOD knows I need all the help I can get with that. During this trip I will have a tuneup in my left shoulder, which needs a MAJOR surgery and I treated with stem cells right before season for pain management to get me through season until i have time for surgery this offseason Also I’m doing a veryyy cutting edge procedure this time where i will go under anesthesia and they will inject stem cells directly into my discs. I’ve have multiple, multiple, multiple ruptures and herniations over the years from training NFL players and fighters in MMA. Couple years ago was supposed to get either a three-level fusion or a rod inserted into my back. That would have changed my life forever and something I’m not prepared for. But right before my scheduled fusion, I threw up a Hail Mary, came down here for stem cell treatment, got the cells and i couldn’t believe it but shortly after treatment I was actually pain-free! I couldn’t believe it. I went to NFL training camp shortly after and people around the league actually noticed a difference in how i was standing and moving and not constantly trying to stretch and do things I used to do for pain relief. Shortly after I actually CANCELLED my surgery!!! My MRI is still completely disgusting so may need a surgery in future but I’ve bought 2 years without a surgery as a result of these stem cells and hoping this procedure I’m doing down here this time gives me many many more years. I’m hopeful. Hope is a great thing to have. Will keep ya updated how it’s going. If you want info on this DM Percy Knox Jr not me! lol. He knows more about it than I do! Btw going from here and beauty of Panama right to #nflcombine where it starts up allll over again. NFL never ends #stemcell #therapy #backpain #stemcelltreatment #panama #panamacity

Jay Glazer

252,987 görüntüleme • 1 yıl önce

Dr. Suzanne Humphries: What if the very method of vaccine creation was its greatest flaw? We're told vaccines are a miracle of modern science. But how are they actually made? It starts by extracting a virus from a sick human or animal. This live, virulent virus then must be "attenuated" – weakened. How? By serial passage. They incubate it through a series of foreign cell lines to force it to mutate. Think: human amniotic cells, chicken embryo cells, and most notoriously... monkey kidney cells. But then, they need to mass-produce it. This is where it gets even more concerning. To multiply the virus for millions of doses, they grow it on rapidly dividing cell cultures. Some of these are: ➡️ Madin-Darby Canine Kidney (MDCK) cells (from a cocker spaniel, made tumorigenic so they multiply forever). ➡️ WI-38 & MRC-5 cells (fibroblasts from human fetal lung tissue, originating from elective abortions in the 1960s). These aren't conspiracy theories. They are listed right on the package inserts. You are not just being injected with a "weakened virus." You are being injected with a biological soup of foreign animal DNA, cell debris, and growth medium residuals. The obvious question: What unknown pathogens hitch a ride? History gives us the answer. For 30 years, a cancer-causing monkey virus—SV40—was injected into millions via the polio vaccine before it was "discovered" and acknowledged. It is now heavily associated with human tumors. And SV40 is not alone. Third-party researchers have repeatedly found stray viruses, retroviruses, and other contaminants that were not tested for. Why? Because you can't test for something you don't know exists. The entire process is built on a foundation of biological cross-contamination. We are playing a complex game of genetic roulette, trusting that no new unknown virus is silently passed along. This isn't anti-science. This is PRO-transparency and real safety. It's time to ask the hard questions they don't want to answer. What are we really injecting? What long-term effects are we ignoring?

Camus

60,406 görüntüleme • 9 ay önce