whygetfat on Nostr: Ulcers, Leaky Gut, Getting Fat, Autism, Cancer Dr. Jack Kruse: "When I was in medical ...
Ulcers, Leaky Gut, Getting Fat, Autism, Cancer
Dr. Jack Kruse: "When I was in medical school, we used to do vagotomies on people for people who had ulcers. We used to think this was a good idea to go in and cut their vagus nerve.
"Then Barry Marshall comes along and says, 'OK, I think it's Helicobactor. I'm gonna prove it.' He looked for an animal model to use. He couldn't use monkeys or gorillas. Why? Because the closest relatives to us have a different gut organization than we have. So what did he have to do to prove it? He had to drink the fucking Helicobacter himself and then scope himself while he did this. [...] He couldn't use a chimp or a gorilla to do this because they don't have the same gap junctions in their gut that we do.
"Turns out humans have a leaky gut by design. Why? Because we're designed to absorb tons of viruses that are in seawater. That's the difference between us and chimps.
"It turns out that those viral elements that we got from seawater played a massive role in encephalization of our brain. That's the reason why we have two frontal lobes and gorillas and chimps don't. It's also the reason why when a human baby is born it's fat as shit, has an immature brain. When a chimp and a gorilla have almost a fully-formed brain and they look like an anorexic individual. Because they don't need the fat to develop the brain. That brings then a new point.
"Is that the reason why people are getting fat in different parts of the world today? Is there something that's causing a cognitive devolution? Is the body reacting like the cancer cell, is going back to a primitive form? We call that atavism.
"I'm going to tell you that to me is the key to autism. That's exactly what's happening there.
"The same thing that's happening in Levin's lab that he's learning about cancer, where there's changes in gap junctions, is the same thing that happens with neuronal migrations.
"Cells, just as I told you DNA has a history of all life, so do cells. Pay attention to what cells do.
"Remember what Becker found, Cameron. He found that in salamanders, in mammals, that red blood cells have the capability to dedifferentiate into pluripotential stem cells by using using weak electromagnetic signals. Then hard stop again.
"Think about what Gurwitsch found in the onion root experiment, that you cannot pass through mitosis unless you have extreme low frequency UV light. You're learning some of the key metrics. These are like the beacons, the signposts.
"So I would tell you the link to biophotons, the link to ROS signal, is tied to the presence or loss of the gap junctions. That brings directly the idea of AMO physics to the cell.
"And it turns out this is the reason why in cancer cells, also size and shape changes, also completely correlate to thermodynamics. It also make sense why mitochondria look the way they do in different diseases. But people are not putting those things together.
"Remember, there's there's micropores on the inner and outer mitochondrial membrane that are acting just the way the cells in Levin's lab are working. But remember, the mitochondria itself is a bacteria. it's not a eukaryote. So you have to begin to realize that how that mitochondria operates within a eukaryotic cell is not going to look the same as a eukaryotic cell that Levin is working you know, with cancer.
"The key thing is, I think what he's focused in on is the morphogenetics. I think he's between Becker and probably Rupert Sheldrake, if you want to know the truth."
Cameron Borg: "I couldn't agree more."
Dr. Jack Kruse: "Yeah. I think that's where he is, and I think he's looking for things that are going to get him to the next level." —Dr. Jack Kruse with Cameron Borg @ 01:36:18–01:40:47 https://youtu.be/2Xfa_V30tR0&t=5778
Dr. Jack Kruse: "When I was in medical school, we used to do vagotomies on people for people who had ulcers. We used to think this was a good idea to go in and cut their vagus nerve.
"Then Barry Marshall comes along and says, 'OK, I think it's Helicobactor. I'm gonna prove it.' He looked for an animal model to use. He couldn't use monkeys or gorillas. Why? Because the closest relatives to us have a different gut organization than we have. So what did he have to do to prove it? He had to drink the fucking Helicobacter himself and then scope himself while he did this. [...] He couldn't use a chimp or a gorilla to do this because they don't have the same gap junctions in their gut that we do.
"Turns out humans have a leaky gut by design. Why? Because we're designed to absorb tons of viruses that are in seawater. That's the difference between us and chimps.
"It turns out that those viral elements that we got from seawater played a massive role in encephalization of our brain. That's the reason why we have two frontal lobes and gorillas and chimps don't. It's also the reason why when a human baby is born it's fat as shit, has an immature brain. When a chimp and a gorilla have almost a fully-formed brain and they look like an anorexic individual. Because they don't need the fat to develop the brain. That brings then a new point.
"Is that the reason why people are getting fat in different parts of the world today? Is there something that's causing a cognitive devolution? Is the body reacting like the cancer cell, is going back to a primitive form? We call that atavism.
"I'm going to tell you that to me is the key to autism. That's exactly what's happening there.
"The same thing that's happening in Levin's lab that he's learning about cancer, where there's changes in gap junctions, is the same thing that happens with neuronal migrations.
"Cells, just as I told you DNA has a history of all life, so do cells. Pay attention to what cells do.
"Remember what Becker found, Cameron. He found that in salamanders, in mammals, that red blood cells have the capability to dedifferentiate into pluripotential stem cells by using using weak electromagnetic signals. Then hard stop again.
"Think about what Gurwitsch found in the onion root experiment, that you cannot pass through mitosis unless you have extreme low frequency UV light. You're learning some of the key metrics. These are like the beacons, the signposts.
"So I would tell you the link to biophotons, the link to ROS signal, is tied to the presence or loss of the gap junctions. That brings directly the idea of AMO physics to the cell.
"And it turns out this is the reason why in cancer cells, also size and shape changes, also completely correlate to thermodynamics. It also make sense why mitochondria look the way they do in different diseases. But people are not putting those things together.
"Remember, there's there's micropores on the inner and outer mitochondrial membrane that are acting just the way the cells in Levin's lab are working. But remember, the mitochondria itself is a bacteria. it's not a eukaryote. So you have to begin to realize that how that mitochondria operates within a eukaryotic cell is not going to look the same as a eukaryotic cell that Levin is working you know, with cancer.
"The key thing is, I think what he's focused in on is the morphogenetics. I think he's between Becker and probably Rupert Sheldrake, if you want to know the truth."
Cameron Borg: "I couldn't agree more."
Dr. Jack Kruse: "Yeah. I think that's where he is, and I think he's looking for things that are going to get him to the next level." —Dr. Jack Kruse with Cameron Borg @ 01:36:18–01:40:47 https://youtu.be/2Xfa_V30tR0&t=5778