The Dr. Lodi Podcast

Episode 151 - 6.8.25 The Truth About Chronically Fermenting Cells: Understanding Cancer's Real Nature

Dr. Thomas Lodi Episode 151

Imagine a world where cancer isn't a death sentence but simply a cellular adaptation that can be reversed. Where Parkinson's disease isn't an inevitability but a toxic burden that can be lifted. Dr. Thomas Lodi invites you into this paradigm-shifting perspective where the language we use determines not just our psychological response to illness, but our physiological one as well.

The conventional medical system has taught us to fear diagnoses and surrender our power to specialists wielding toxic treatments. But what if we recognized that these "diseases" are actually adaptive responses by our bodies facing environmental challenges? Dr. Lodi explains how changing our terminology from "cancer" to "chronically fermenting cells" transforms our understanding from fighting a mysterious enemy to supporting metabolic restoration.

When treatment becomes necessary, approaches like insulin-potentiated therapy deliver chemotherapy with precision rather than destruction. By exploiting cancer cells' increased insulin receptors, treatments can target damaged cells like a dart hitting a bullseye rather than a grenade destroying everything in its path. Yet Dr. Lodi emphasizes that addressing the causes—removing toxicity and providing optimal nutrition—remains paramount.

The modern environment bombards us with unprecedented electromagnetic frequencies, compromising our immune systems and triggering adaptive responses we label as disease. From pneumonia to parasites, from breast cancer to brain disorders, the fundamental approach remains consistent: restore balance rather than attack symptoms. Therapeutic protocols featuring vitamin C, glutathione support, detoxification, and nutrient optimization create conditions where the body no longer needs adaptive strategies.

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This episode features answers to health and cancer-related questions from Dr. Lodi’s social media livestream on Jan. 19th, 2025

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Join Dr. Lodi's Inner Circle membership and unlock exclusive access to webinars, healthy recipes, e-books, educational videos, live Zoom Q&A sessions with Dr. Lodi, plus fresh content every month. Elevate your healing journey today by visiting drlodi.com and use the coupon code podcast (all lowercase: P-O-D-C-A-S-T) for 30% off your first month on any membership option.

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Speaker 1:

buddy cup. Good, uh, sunday night live and monday morning live here on this side of the world, and I am trying to get everything together. I think I did. I finally got it. This is hard today. I'm so sorry, gosh, here we are. So I'm late again. That's because I couldn't get this set up. So, anyway, I'm glad you could join us. We got at least a few people here. I don't blame you if you went to, went to bed and you said why stay up and watch this guy? Anyway, let's make today a good day.

Speaker 1:

I wanted to say a few things you know, as usual, to you know, just kind of to remind everyone what's going on. We have the Sunday Night Lives and, as you know, we also have three groups. The three groups are the health and healing group. The other one is the parasite group. The other one is the parasite group. The other one is the cfc groups, which some people refer to as capricorn or sagittarius or cancer or something like that. I think it's cancer anyway, but it's really called chronically fermenting cells. Good morning alice and good morning everyone. You know, yeah, I'm here, made it. That was very difficult and thank you for hanging in there and being there. So, uh, anyway, the content of these groups is incredible. Now it's really growing. For those of people that are in the CFC groups, you have the opportunity of also, in addition to me, doing Zoom meetings with you and answering discussions on your situation and CFCs in general. But you have the opportunity of joining Kathy's Corner.

Speaker 1:

Kathy is a psychotherapist who's been with me for a few years now, and it's a place where you all get a chance to just forget all the tests, forget all the treatments and all that stuff. But let me tell you how I feel and that's what we do. We open up, we share about it, we find out how we're really feeling and thinking about it all, and we find out that there's other people that are feeling and thinking the same things and we're not alone. And it's a wonderful thing. Kathy's wonderful, everybody loves her. And the other one is Darren, who's a kinesiologist, the only one of a kind in the world.

Speaker 1:

Kinesiology is a branch of physiology that specializes in muscles, and muscles are kind of important. It's how we get around or it helps us steady ourselves while we're sitting on the couch, but anyway, our muscles are a big part and that's where metabolism starts and everything just gets going. So anyway. But when they're being appropriately used, your immune system it goes through the roof. So, and you develop type two muscle fibers and you beat something that happens to all of us.

Speaker 1:

It's called frailty. You know, one of the real causes of death in elderly, the most profound is frailty, and it also happens to people who are sick and just unable to do what they need to do. Hi, kelly, Good morning, thank you, good evening. Anyway, it's so good to see you all here, yay, fantastic. And I see a message in Russian, and that's great, and if I could only translate that I would be able to understand it.

Speaker 1:

Elisa, who said that oh, that's Montez, montez, I think you should go somewhere where you're happy. You're not happy, shut up. Seriously, I'm already pissed off. What? Well then, you shouldn't be here. Why would you do that to yourself? Come on, you like yourself more than that. Don't expose yourself to that kind of stuff, um, but anyway, so, so at the CFC group, then we have the parasite group, and the parasite group and the health and healing group have access to, as I said, everything except Kathy's Corner, but Darren the kinesiologist, vanessa, who's a nutritionist and a health coach and a yoga instructor and a meditation instructor, and she knows how to take you from where you are to where you want to be. She helps you get the tools that you need, both in mind and in action. And then we have Donna Peroni, and she has been a raw food vegan for about 36 years now An amazing woman, and she will also show you how do I make this stuff taste good so I can eat it, and she'll teach you about why. She's also a colon therapist, which is beautiful because she takes care of both ends of that long tube that sits in the center of our physical being.

Speaker 1:

Now let me just say this one thing here. So here we are, and in addition to all that, we're doing webinars, and I did one on vitamin C, which is everything you wanted to know and everything you didn't want to know, but it's everything about vitamin C and that's available on the website, and so we're having webinars like twice a month, and so if you're a member, of course, there's no fee and they're available to you all the time and it's really good. We kind of need to know what vitamin c is if we're going to use it. We need to know what nadh is if we're going to use it, or nad plus or whatever, whatever therapies we're going to do, I'm going to do continued webinars on them, and I'm going to do that because, um, I don't want to answer questions really, because that won't help you. But what will help you is to give you the information and the understanding so that you can answer that question and all the other ones that will arise.

Speaker 1:

So my goal is for you to have the understanding and with that you're going to find out that you'll never need another doctor the rest of your life, because you'll be your own doctor, and that's not really that. I'm using that phraseology because that's all we have in our language. But you know, doctor means oh, that was doctored up, meaning it was changed or something right, you fixed it. So that whole concept needs to go away. But, in other words, you'll be your own, you'll guide your life of health, and when that health gets imbalanced, you'll be able, you'll recognize it and you'll know how to deal with it. And so you'll have to go see the technicians when you broke your leg or you're having a critical situation. They're excellent at that. That's where the allopathic MDs come in. They're excellent at that kind of situation.

Speaker 1:

Okay, but that's about it. So there's a lot of content on there and it's growing even more. But that's all available to you if you're on Health and Healing or Parasites or CFCs, of course, and remember it's at DRThomasLody on Instagram, facebook, youtube, linkedin, et cetera. Rumble, yeah, I'm not sure what else there is, but it's drthomaslodymd at the end on X and TikTok. Okay, I did it, got it all done, all right, cool, so let's get into questions. Okay, and, by the way, normally I have a chance to even like go over them and see what they're going to be. I do that usually an hour or two before, just so I know what we're going to be talking about. But I didn't have a chance, so I'll be seeing it for the first time.

Speaker 1:

The first question is from Jolita and her question is over the last 10 years, I've always been following Dr Lodi, always for others. Now I'm in Phuket in a hospital with pneumonia, not CFCs. Luckily, they gave me antibiotics and steroids and what else. I haven't had any of these medications in more than 30 years. There are so many people with pneumonia at the moment. What is the best way to deal with it? I am not allowed to fly home to New Zealand yet, whoa. Okay, jolita, I'm happy you wrote and you're here in Phuket Me too.

Speaker 1:

Well, okay, what is pneumonia? Pneumonia? Okay, our respiratory system begins with our nose and our mouth, of course, and that's where the air goes in. And it goes in through the bronchus and the trachea, the bronchus, and they split off into little bronchioles which go into the lung matter, the parenchyma as they call it. The parenchyma means the actual working part of a tissue. So the parenchyma of the kidneys is the, or the glomeruli. The parenchyma of lungs is actually those little sacs, alveoli, that exchange gases and it carries, it's connected to the bronchial, which goes to the bronchus, and those little air sacs in the lungs they diffuse back and forth into the blood. So I mean, that's it.

Speaker 1:

So pneumonia is when you have large colonization of one particular microorganism that is kind of taken over. Instead of there being a well-balanced like we have a gut biome, instead of there being a well-balanced biome, this one group takes over and it's called by the medical profession as an infection. So you know, if you have a little abscess on your hand or arm, that you know that's what they're calling an infection. And what an infection is is an overgrowth of a particular organism in a particular area. So pneumonia is having it usually refers to in general a bacterial overgrowth in the lung, and when we look on x-ray we can see there's a big area there or a small area, whatever it is, but it's in the parenchyma, not in the bronchial tubes. And what is it doing there? It's compromising your breathing. Not only that, those microorganisms which are in that little pocket there are diffusing into the blood. So your risk of having an overwhelming colonization in your blood is there.

Speaker 1:

So it's kind of a nasty thing. You wind up coughing up phlegm and it can be green and yellow and you're coughing it up or you're not coughing, you're not able to cough it up. That's another situation. The other kind of what they call pneumonia is a viral pneumonia and it's not at all the same. It's not like a pus pocket in your lung parenchyma, because viruses don't act that way, but you can have a viral pneumonia.

Speaker 1:

So you're probably, I think, talking about a bacterial pneumonia and you're saying that there's a lot of it going around now. I wasn't quite aware of that, but I thank you for telling me. I need to look into that. But why are all these things going around? Why is it that almost everybody I talk to is having trouble sleeping. They're having headaches, you know they frequently are coming down with the body aches and lethargy and weakness, and you know things that we would in the old days was called the flu, and now we're calling it COVID. So I don't know.

Speaker 1:

Anyway, but what's happening is we're being exposed to electromagnetic frequencies. It's so intense it's almost like we live in a box that's being irradiated. It's crazy how our exposure has increased, because I think, if, if you realize that in the year 1900 we had, uh, just what is called ambient or naturally occurring electromagnetic frequencies from the sun right, because the sun is a generator of electromagnetic frequencies, right. And then there's, uh, there's the extremely low frequencies, which are the ELF. Those are low frequency and they cause a lot of damage to biological systems, as do the higher frequencies, emf, which can go up to now.

Speaker 1:

We've graduated to 5G, and I think someone has told me that we even have 6G now, which is kind of bizarre. I didn't even know there was a 6G and I heard there's actually even others. Let me just make sure I get this here. Excuse me one second here. There it is, is that it? Yeah, okay, all right, now what do you do about it.

Speaker 1:

They're giving you antibiotics and steroids. So the reason they give steroids is usually there's the immune system is reacting to this thing that's going on. The immune system is trying to restore the balance of the microorganisms and which would mean eliminating that pocket of colonization. Thank you, hammy, mean eliminating that pocket of colonization. Thank you, hemi. Okay, so in its effort to do that and combination of what's going on in the lung, there can be wheezing and constriction of ability to breathe and you know lots of other symptoms which are really the immune system trying to do its job, and so the steroids eliminate that. And all of a sudden excuse me, I don't have the money the steroids eliminate that, but unfortunately the steroids also. They're suppressing the immune system system wide, so they're really an immune suppressant, which is not a good idea.

Speaker 1:

Let me, there we go. It's not a good idea, but it makes people feel better. And this happens in a lot of conditions when a doctor is in a situation with a patient that they're working with and they haven't looked for the cause. But then, because they don't look for the cause, they just look for which hammers they can use to knock it down. But when they're in a situation that they don't really know how to do steroids. That's like, okay, let's do steroids because that will slow everything down and they'll feel better for a while, they can get them out of my office, but whatever, that's what they use. So the antibiotics are trying to kill those microorganisms.

Speaker 1:

Now there are situations where you've got to use antibiotics and that kind of makes you think, well, wait a minute. Then that means you're subscribing to the germ theory and yeah, I'd like to talk about that at some point, about the germ theory and all that. But, for instances, you have a bacterial overgrowth in your blood or a fungal overgrowth in your blood or anywhere else on your body and it's causing a problem. Then there's times when you've got to use the antibiotics intravenously or antifungals. So there are times for that. But that doesn't mean we're subscribing to the germ theory. That means we're using them to help restore balance. The problem is, those antibiotics are also killing the healthy bacteria that we need. And are they there everywhere? There's no place in us that doesn't have them Right. Like 100 trillion in our gut, 100 trillion, 100 trillion in our gut. We have like 44 species on our forearm.

Speaker 1:

When we talk about a microbiome, we're talking about the differing percentages of microorganisms in a particular area. And since microorganisms are the are the of life out of, you know, it's the microorganisms that that, you know, keep carbon moving and oxygen moving and nitrogen moving and sulfur moving. They keep these cycles alive. Sulfur moving, they keep these cycles alive, which are the foundations of life. Are made up of these atoms and those cycles that keep them restored and renewing and being used is pretty much dominated by the microorganisms. The microorganisms also give us their metabolism in our systems, happen to stimulate our immune system system, make the immune system produce most of the serotonin that is necessary, for it's a neurotransmitter. It's also called the feel-good hormone and, um, you know it's, it was me, it's me like that's morning. Yay, I'm ready for, ready for all that.

Speaker 1:

You know it's a combination of cortisol and other things, but but serotonin plays a big part in people who get depressed, even though they get what are called serotonin reuptake inhibitors, which blocks serotonin from being broken down, which keeps more serotonin around. So the implicit of depression is that it's a lack of serotonin. But that's not it. However, by giving these SSRIs and they increase the amount of serotonin available people don't feel, as you know, unable to do anything and all that. It kind of lifts them out of that, although it compromises the body in so many other ways that it's almost questionable about whether or not it was worth it.

Speaker 1:

And there are really other ways of doing it. First of all, restore your microbiome. Get a healthy microbiome so they can produce it 90% of it, and the rest is you have to be able to as well, but anyway. So, but don't work on restoring your physiological function, which would be my goal is to say how can we get your physiology back balanced and functioning, because then you'll be in a condition that we call health, yeah, so. So the anemones and the steroids are kind of what they do. It's like the only tools they have. The other tools they might have is, if you're wheezing because of what's going on in your lungs, they would give you something nebulized to breathe in that would dilate your bronchioles so that you can get more air exchange, because the wheezing is a decrease in air exchange. It's basically whistling in your lungs. So there's those kinds of things too.

Speaker 1:

And pneumonia, by the way, is distinguished from a bronchitis, which means that you have this, this sort of overgrowth, inflammatory process going on in your bronchial tubes and not your lung. So, anyway, those are just terms and they're based on what I just said, the anatomy location. So, um, what do you do? Well, first of all, whatever they're doing for you, if the antibiotics, if you were so sick that you needed to be admitted to a hospital, it sounds like probably your vital functions were compromised, you were, you know, I don't know coughing and you didn't have enough oxygen and you were mentally uptunted. I'm not sure what would have happened with you coughing up a lot, just weak.

Speaker 1:

So at a time like that, you give the antibiotics. They do eliminate a lot of the bacterial overgrowth in your lungs and you can start to get better. Because when you're at the point where whatever's going on in your body in terms of a microorganism overgrowth, when that's impacting a vital function like breathing, it's something you've got to take care of now. So you know that's where the antibiotics would come in. But as soon as you're feeling better, you're breathing and you've got the energy again, you know, then you would probably consider leaving and then going to a center that could help you restore your physiology, where you would get intravenous vitamin C, other intravenous botanical non-toxic substances, you know, ozone, curcumin, all these things that are good for people with CFCs are also good for any condition.

Speaker 1:

All right, because, remember, the goal is to restore balance of physiology. The goal is not to get rid of anything, because we need to understand that that thing that we're trying to get rid of exists because there's an imbalance, it's a manifestation of it. It's just a reminder that that's what's going on. So, although we focus on that, that's not foundationally what's going on. So that's what you could do. And you're in Phuket, so there are, just look them up. There are several healing centers, alternative medical centers, medical treatments where they give intravenous vitamin C and other very important things. So the other thing you can do is cleanse right now, because you're obviously toxic. Now you've got the antibiotics, or even more toxic.

Speaker 1:

So when you get out of there and you have control of your life again, you can do a three-week juice cleanse, but it might be hard because apparently you're on vacation and what is it? You're not allowed to fly home yet to new zealand. Did they tell you what condition you have to be in so you can't fly? Usually what it is when you get a fit to fly a letter from a doctor. It's saying that you are in good health and well enough to sit on a plane and you're not going to be harmful to other people. And so if you can't get, if you are obviously sick, if you don't look sick, you'll walk onto the plane and no one will ever ask you anything. I mean, if you're not sitting in a wheelchair or obviously incapacitated, you know so, then they would give you a fit to fly and then you could fly. So I'm not sure what you need for that or where you're at. So it's hard to answer your question completely. All right now, cindy, one second please, sorry, okay.

Speaker 1:

So this is Cindy and her question is on chemotherapy and it says in what cases would you recommend low-dose chemotherapy? Besides low-dose chemo, what other natural compounds would you recommend specifically to target and kill CFCs, specifically to target and kill CFCs? All right, so, cindy and everyone else who might be interested to know the answer to that question, what happened to me? Sorry, all right. So, okay, what does that mean? Chemotherapy, first of all. What is Cindy talking about with low-dose chemotherapy? Why would you give somebody low-dose chemotherapy when you really need to get rid of it? You don't want to waste your time.

Speaker 1:

Well, as it turns out, the standard chemotherapy that's given is called maximum tolerated chemotherapy and they learn through their usually their initial, what they call preclinical studies, which are when they're working with animals, and for the most part that's preclinical studies, which are when they're working with animals, and for the most part that's preclinical. They find the amount of chemotherapy that's the most they can give, because the more they give, the more it's going to be able to get into the tumor without killing the person, and so that's what they give. So it's called maximum tolerated and it's so powerful because multiple effects, you know, one is shrinking tumors, hopefully, but there are other ones that you didn't really want Ensuring metastasis, ensuring it suppressing the immune system, harming the gut so that you're nauseated and not even able to digest your food, if you're able to get it in, and I mean just also're able to get it in. It's unbelievable what it does, but a lot of people are strong enough at that particular time not to really get really sick and that's amazing that they withstood that, because one of the effects it does is shrink the tumor, which we want. So what they found was, since there were so many serious effects from it, they started giving it in lower doses to see what it would do.

Speaker 1:

And initially they found that low dose, very low dose chemotherapy, you know maybe 5% or less at a particular rhythm, would block blood vessel growths. And if the tumor doesn't get blood vessels doesn't get blood, it can't, it can't exist and it certainly can't get bigger and grow. If a tumor even gets one millimeter bigger, it needs more blood. And so the process of angiogenesis angio meaning vessel genesis meaning initiation of the birth of. So angiogenesis is new blood vessel formation, so that's happening. So it turned out that the low dose actually would block that, which is fantastic, because if you can do that, then the tumor, which has really dysfunctional, kind of like spaghetti blood vessels, is going to eventually fail because it can't control what's going on. And you wind up getting uh and it dies and it's so the tumor would die but also during that time wouldn't be able to grow. So that's how the uh low dose was, was uh, that's what they were looking at and that's what they were measuring.

Speaker 1:

And instead of keeping it, instead of calling it low dose chemotherapy because the reason they don't want to call it low-dose chemotherapy is because you know what it means. And if you know what it means, that means that makes you like them and they need to know more than you. They need to be smarter than you because you're going to pay them money and also they need to maintain their prestige and all that sort of thing. So they changed the name to metronomic chemotherapy. Isn't that great? Because if someone here is metronomic, they're going to not know what it is, but they're going to think these guys are really smart. And so what does metronomic mean? You all know what a metronome is.

Speaker 1:

Okay, some of you may not, but if you're taking piano lessons or any other kind of music lesson one of the critical you know one of the foundations of music that we may not be aware of is the rhythm. We are, especially if it's the kind of music that makes you want to dance, but we're not aware of it. We're not aware that there are instruments in the presentations of music that are keeping the rhythm, and the rhythm is kind of the structure of music. So even in a classical piece that you may not be hearing any drums, the instruments are giving it a rhythm. Of course we know. You know, like the jazz, the bass, and even in rock and roll with the bass, there's a lot of rhythm, but mostly it's the drummer and it gives rhythm.

Speaker 1:

So when you're learning music, you've got to learn to read notes and you're going to find out that every beat has a certain rhythm or a certain periodicity. And so you learn the rhythm right and you keep everything at three, four times. So it's one, two, three, one, two, three or four, four times four, one, two, three, four, one, two, and we keep it like that. But in music, when we're listening to it, like jazz, rock and roll, everything we're hearing the drummer. The drummer's keeping it, it, giving it a foundation, can stand up. It's got a skeleton right.

Speaker 1:

So anyway, in order to help you learn your musical instrument, there's this thing. It's usually looks like a triangle with four sides and on the three sides, yeah, like like a pyramid, and there's a. Inside, there's a, there's a metal, thin metal, thin piece of metal, and it's got a weight on it and that weight determines how quickly it's going to fall. So you set the metronome at a certain level Tick, tock, tick, tock, tick. Now they have electric ones, but that was originally how they had it. But basically it's just keeping you on rhythm. So rhythm, remember I said earlier, they give the low dose at certain specific intervals. So if it was every other day, it was a third day. So it's a rhythm, even though when they give the maximum tolerated chemotherapy, they give it in a rhythm. It's a bigger, it's a wider rhythm.

Speaker 1:

So you might get the chemo every three weeks. Why? Because it takes it takes at least two weeks to get up. You just got punched down to stand up, right. So because of that you need to have been recovered enough to get hit again. So they might have a two-week and then a two-week and then you get the treatment and then another two weeks or three weeks. And that depends on how toxic the chemo is right, because because it's extremely toxic, you'll have to have a wider interval between treatment sessions. So that's metronomic, but we're just low dose chemo. So with the low dose they actually have changed the name. They've got people thinking in terms of metronomic chemotherapy and you, the average person, is going to say I don't know like must be good, because that's all it is now low dose chemotherapy.

Speaker 1:

They found out that it not only will uh block and filial the lining of, of of a blood vessel, uh growth and all that, but it also has its own effects. It's also doing what the high dose would do, but it's not damaging that much because it's a low dose, maybe 10 percent, five percent or even a little bit. Every day, for example, you know taking uh, you know 50 milligrams orally of of a medication which they do a lot of. You're're doing it daily. So it's a and it's low dose and even though it's oral, it's still by definition a metronomic part of metronomic chemotherapy. So what's been learned is this it's very interesting. It's almost a homeopathic concept and you all know what homeopathy is, okay, what it is basically. You know it's more complicated, but fundamentally what it is is.

Speaker 1:

It's been observed that any substance that has an effect on biology will and that effect we're talking about a damaging effect. So, for example, there's a plant called Nux vomica that comes from that plant. So if you eat this plant, you bone it. So what's been found is that if you can take some uh like oil or essence of it, put it in an amount of water and then you know, seal it like just put a drop in there and then hit it against your palm, that's called succussing it. If you do it 10 times, it's 10x, 100 times, it's 100x, and then you take out the same amount from that and you put that in the in water, whatever it was, whatever water you were using, like it was 10 percent, uh, 10 cc's, 5 cc's, whatever it is and then you succuss it again. I'm sorry, the other stuff wasn't 1x, that was just the succussions.

Speaker 1:

Now, the 1x would be that you, you did it. You did would be that you succussed it 10 times and now you're getting another drop ready. So that was 1X. 2x would be having done it the second time, 3x would be having taken it out and doing it the next time. Well, by the time you get to a certain dilution, because you're taking a little bit out and putting it in water, it's getting more and more diluted. You get to a certain point where, actually, if you went in with some equipment, you wouldn't even be able to find that original molecule anymore. It's no longer there. However, its effect, its energy is still there. So, from a low dose of the same substance that caused one to vomit, it now will stop vomiting and prevent vomiting. Okay, so that's kind of fundamentally homeopathy, and that's what they found with metronomic chemotherapy that it actually can be immune-enhancing and have some effects that are really beneficial.

Speaker 1:

Now, prior to all of this happening about 100 years ago was it 100 years ago, no more than 100 years now? 100 years ago Was it 100 years ago, no more than 100 years now there was a skinny Mexican doctor named Donato Perez Garcia and he was in the Army and anyway, I'm not sure if this happened before you joined the Army or not, but he wanted to. It must have been after, because anyway, I don't know his exact medical history like that but he started to use insulin. Insulin had been discovered prior to that, but they finally found a way to get the insulin from a pig and give it to a human. So he said he used it to gain weight. He wanted to be giving himself a shot before every meal. And I think what was it? 10 units, which is a pretty a shot before every meal. And I think what was it? 10 units, which is a pretty fair shot before every meal. And he found that he did gain weight and he did get stronger and bigger. So he said, wait a minute. That means the insulin is somehow helping the food I eat, the nutrients, get into the cell. So he saw it as a delivery mechanism. So he says, let me try that with something else the cell. So he says he saw it as a delivery mechanism. So he says, let me try that, something else.

Speaker 1:

So he took low doses of uh one of you know a couple of the only poisons. They didn't have any poisons in those days so he took a little bit of arsenic and a little bit of mercury and used the insulin and what, and was able to actually eliminate the uh, the syphilis organism that had gotten into the brain and that's called tertiary syphilis. And tertiary syphilis back in those days was the most, the most the dominant reason for psychiatric, psychiatric hospital admissions in those days. And so this was a big deal. He was invited to the white house and all that, but he, he did it with other conditions. So you give a little bit of something with the insulin, so the insulin would open the door and get it in there. So you give a little bit of something with the insulin, so the insulin would open the door and get it in there, and then that little bit of whatever it was could have its effect.

Speaker 1:

And in 1943, one of his officers above him asked him to treat someone that CFCs of the lungs. It was a woman where the breast because she was getting married and they didn't want to have to remove it breast because her dress size was already made. I mean, this is true, I heard it from the, not himself, and so they asked him to. They asked the, not the Perez Garcia to try the insulin and he did and, by the way, that was 1943, 1946. He, the one that's alive today, is Donato Perez Garcia III. So his father, you know his father, who was the son of the original guy, went on to do the same kind of work as the original Donato Perez Garcia, kind of work as the original donato perez garcia, um. And then the second son, which is the one I know, the third, um, somehow, I think yes, this woman came to him for treatment. She's now standing her like I don't know mid to late 80s or something, um, I don't. So he was kind of blown away and you can imagine why.

Speaker 1:

Here's a woman, first person ever treated with IPT in the world before they had chemos, and it's still alive After what. I don't know how old she was, but let's say she was 18 or 20 or something like that. So it restored the whole system, she got healthy and she lived on. So that's IPT and IPT being so non-toxic because insulin drives it into the cell, into the CFC, so you can give lesser doses. Yeah, so it has all of the benefits that we talked about with metronomic chemotherapy, but it also has additional benefits in that because CFCs have many more insulin receptors, because they need more glucose, because they're fermenting and fermentation is a very inefficient process for producing energy 19 times less than our normal cellular respiration, which is in the mitochond mitochondria. So they need 19 times more glucose if they're going to survive.

Speaker 1:

So that they go through all sorts of changes. They upregulate this, down, regulate that. In other words, they change their genetic expression. What does that mean? Genetic expression is when you open some uh enzyme systems and others you shut down, or or signaling systems or whatever it is. So you've turned them on, you've turned some on and you've turned others off. You've just silenced them. So what's being expressed in your genetics has changed, but that change in the physical presentation, which is also called epigenetics, you now have a genetic expression that will support um, that that supports it makes it easier to happen for the cfc's to develop, and that's what happens. They have search epigenetics. Basically they are in an adaptation, all right. So, and since cfc's have all these extra insulin receptors because they need more glucose.

Speaker 1:

When you get ipt, what happens is you come in having fasted at least the night before, I think. Some places think it's six hours or something, but the goal is just to get in a place where your body's no longer processing food. That's in your body, right, and so if it's a six-hour window, so it's the last time you ate, versus a 12-hour. So the longer that window is there's going to, the longer that window is there's going to be less and less, until there's no processing of any nutrients, because there's nothing left. It's all you know. It's all been digested in one way or the other. So the um, so the. So the insulin brings in more uh, because it has more receptors.

Speaker 1:

When you give the insulin to someone who's in a fasting state, the CFCs have more receptors, so they grab more insulin and they open their doors sooner. When they open their doors, what's happened is the amounts of chemotherapy goes that way, like if you had a pipe system and you had a few pipes turned off and only these pipes are open. So it wind up going down there. So that's what I'm sort of funnels into the tumor, which is great. So it's a way of targeting the tumor and not targeting, and not not hitting, all the other healthy cells around, right?

Speaker 1:

So you know, one of the great analogies that I see is that, let's say there was something you really didn't want in your house, kind of like a deadly scorpion or whatever on your wall. Well, you could, like, get a dart if you're really good with darts like that you could capture it, throw it away or give it a new home somewhere. Or you could get a hand grenade, throw it at the wall and blow out your whole kitchen and you probably killed the Scorpio or whatever. Well, that's kind of the allopathic medicine just throw that hand grenade and then the chemotherapy is just getting that dart right into it like that, because then you get to keep your kitchen, you get to eat, uh, which is a good idea. So, um, that's, that's the way of viewing the targeting of it with the insulin. So insulin helps to target it right and you're not knocking out the stove and you're not knocking out the window and the faucet, okay, okay, you're just doing that. So it's targeted and because it's so relatively non-toxic, it's got like 5% of the same effects. That a standard would be. Yeah, but it the what was I saying? Anyway, but it's because it is that, in effect, that non-toxic.

Speaker 1:

You can give it at more frequent intervals. You don't have to wait two weeks or three weeks. You can do it twice a week. You could do it every other day, but you'd have to get really low doses because there is a cumulative effect regardless of how little you give, right? So what I've seen is that there's pretty much no effect on people, negative effects on people who get it at the beginning. But if they're getting it, let's say they're getting it twice a week for eight weeks by that time you've probably got more than, in total, a full dose. You didn't get it all at once, so you didn't get the bomb, but you've accumulated it and then you start to see the white blood cell count go down and some of the other problems that are usually associated with the standard, but much less. You don't see hair loss, you see. I mean they might have some thinning, but it's nothing like what you see with people getting standard. So that's basically that makes it metronomic, because it's in specific intervals. So it's insulin potentiated metronomic chemotherapy. You could say low-dose chemotherapy. It doesn't sound good. It sounds better if you can say insulin-potentiated metronomic chemotherapy.

Speaker 1:

So in what cases would I recommend it? And that's a very good question, since it sets up metastasis, damages the immune system, damages the gastrointestinal system, damages a lot of systems. I'd rather not give it. If I don't have to, I won't. And the reason I don't think that, just because there's a tumor there, I have to do it, is because we all know the apple tree metaphor, right? Everybody who ate an apple off that tree died. So you call the tree doctor, the tree doctor comes over, cuts off all the apples. Did we solve the problem? No, because next fall there'll be a new harvest. So the problem was not the apples. The apples are a manifestation of the problem.

Speaker 1:

And so to surgically remove it, or to bomb it with chemicals or to irradiate it, so what? Because even someone who has what's called stage one, which is just an area of malignancy in any kind of tissue that hasn't really disturbed the architecture of that structure, is Wait a minute, I didn't get enough sleep last night, sorry, um. So anyway, let me, let me get back to, you know, the insulin potentiated therapy. So, so, basically, so, so let's, let's look at that in total. What have we done? We've, we've targeted the tumor, even if they're small tumors. And we're getting the chemo there, we're not getting it elsewhere. And we're also getting that other positive effect which we found out from just standard metronomic chemotherapy, and that is you can eliminate new blood vessel growth and stimulate the immune system, which are kind of good things. So you're getting those benefits as well.

Speaker 1:

And so let me finish the thought I had before. So stage one is where it's, just that's where it is. But even if someone has stage one, it hasn't yet disturbed the architecture, it hasn't gone into the limbs and it hasn't gone to another organ. Even if it's at stage one, it's already got an unknowable amount of microscopic metastasis, if you will, and metastasis means spreading away from the origin. Metastasis, if you will, and metastasis means spreading away from the origin. So you know, if it started in the breast, it's already those little microscopic ones, because it takes at least eight years for a tumor to grow, usually Except. Pfizer came up with a way of actually helping that happen a little quicker. Moderna helped them too. So yeah, so that's the thing.

Speaker 1:

So when they say you're stage one, grossly in other words, looking at it from a large perspective you're stage one, but microscopically you're already stage four. So we have to understand that and that's why when we're talking about psychoneuroimmunology, right, we're saying, don't use the word cancer, because that gives you no information. Use the word or the acronym or the phrase chronically fermenting cells, because that is what's happening and by knowing what is happening you can actually devise something to resolve it. But when you don't know what it is and you're calling it cancer, then you don't know what it is and all you have is fear and that's going to cripple your immune system. So that part doesn't work. But also doesn't work as any of the words associated with that that are going to give that meaning, such as staging and prognosis and treatment and complete pathological cure or partial or there's many different phrases they have, but they all support that concept of the word, of that astrological sign which is telling someone.

Speaker 1:

When you hear that word, when someone says you have, they just said you're going to die Same thing. And what that produces is an extreme fear. And the way and the effect of fear physiologically is that there's a part of our brain called the amygdala which manages fear. It gets so lit up working that it actually blocks its connections to other parts of the brain, like the prefrontal cortex where we make decisions, so that fear eliminates your ability to make a rational decision. Number one and number two that fear cripples the immune system and it does all sorts of things. All right.

Speaker 1:

What supports that word, that we're talking about, that astrological sign, are all the other parts of that paradigm, which is the disease paradigm, which says you've got this thing and you have to get rid of it. Right, and that's not what a tumor is. You didn't get a thing. What's happening is these tissues in your body lost a certain percentage of mitochondria and they're adapting. And that adaptive process is making energy without the mitochondria through fermentation, and they're good at it, so they're chronically fermenting cells. That's what is happening, okay, and that you know. It's important to know what is happening.

Speaker 1:

Uh, instead of having this monster in me so there's nothing in you you have to get rid of what you have to do is change the biochemical environment in which your cells live so that all their needs are being met and they no longer have to go through that adaptive process. And that's true for anything, whether it's diabetes, because you're eating too much, too many foods to cause increased glucose in your blood, stimulating insulin and all that sort of thing. So instead you know, and then they call that diabetes. So instead of taking a drug to get rid of the diabetes which they never get rid of, by the way, you get diagnosed at the age of 12 and you still have it at the age of 82. But it's to just not make that adaptive process necessary.

Speaker 1:

And how do you do that? You stop eating the things that would be causing your blood to have elevated glucose. So if you don't have the elevated glucose, I mean, you will have an L. Everybody has an elevated glucose after eating. It's called postprandial because you're absorbing the glucose. But that's kind of a natural, a natural rhythm, right. But it's what if you're eating it all the time, or the stuff you eat is lasting a long time and all that's going to make your insulin go up and it changes the whole biochemical dynamic between insulin and glucose, which is one of the foundations of the underlying chronic inflammation that we see in all degenerative conditions. So that's why keeping the insulin-glucose dynamic healthy is basically going to have a positive effect on any chronic condition, whether it's osteoporosis, arthritis, crohn's, you know, cfcs, heart, right, any of them because they're all fundamentally having a chronic inflammatory process which keeps it alive, and it's kind of like the oven or the you turn the burner on the stove, so you know.

Speaker 1:

So let me, let me, let me just get back to some of my when I would do it is when a because, remember, if I, if I don't want to just cut off one or two apples and then have it come back, that's really not going to be, that's not what you want, that's not what I want. So what I like to do is stop, is change everything so that we start producing good apples. All right, so so unless the tumor apple is blocking a vital function, or about to block a vital function, such as breathing, eating, bowel movements, et cetera, or excruciatingly painful, you can't deal with it in any way. There's a few reasons. The other one is in your skull. You can't grow very far. So situations like that, we've got to move quickly.

Speaker 1:

Then I would use the IPT and with some people also, they're not having any compromise of their or potential compromise of vital functions, but it's not really responding to some of the other therapies like intravenous vitamin C, intravenous curcumin, intravenous quercetin, intravenous ozone artesanate. There's a DCA, there's a lot of those, and there's systemic hyperthermia and local hyperthermia. There's all sorts of ways of dealing with it. Yeah, so let's see, I think we answered Cindy's question for the most part. So that's when we would use it, and then usually our goal, my goal, is to use it to a point. I want to do this as short a time as possible because it does have a toxicity. It's a small one, but in this case the risk-benefit ratio shows that it's more important to use this because we're going to get more benefit than we are going to develop any any problems from it. So you guys say, well, because let's go for that, all right, so if we can just keep it down to six weeks, four weeks, eight weeks, so that that's usually the way we think. Um, so if someone's got, you know, widely disseminated, we would probably use it for a while, but we'd also have done all the other things that we're talking about, that we talk about, from cleansing and all that. And then also, you have to remember that we have to make the person who's going through this positive be doing it with gratitude, right, instead of drinking the green juice or whatever they're doing. All right, you know we have to get involved. So if somebody really wants it, they come. I really want chemo, but so he's okay, all right, we're gonna do all this other stuff, but we're gonna use low dose with insulin because you don't want someone to be in your, under your care and they're really unsatisfied because you're not giving it anyway. All that negativity is going to be suppressing the immune system, so that's that's important not to allow that, all right. So it doesn't necessarily always have to be that we're we're uh about the impact of auto function or excruciating pain and all that it can be. The person really wants it, um, anyway, but I work with that as well, of helping them realize that they may not be needing it, but when you use it it's incredible. It's incredible and I've seen. You know there are times that we need it quite often. Yeah, all right. So I got you there on Cindy.

Speaker 1:

Now here's Dr Jyoti. It's about breast CFCs and she is saying let me put this here. She's saying hello, sir, I'm diagnosed with triple negative breast CFCs in 2024, and it was metastasized to the lungs. I've taken NAB paclitaxel, which is where they change paclitaxel, which is taxol. It's a type of chemo, right, and they make it so it's more targeted. Targeted and uh, erbulin, with which both got effective after ineffective. After a few months there are big lumps in both of my clavicles these bones here clavicle regions, and also in my right axilla armpit. Now my medical oncologist is asking me for a biopsy and a third line of chemotherapy. My BRCA1 and BRCA2 exams were negative and PDL score was 5 over 10. That's why I could not take immunotherapy with chemotherapy. Please help me as giving me proper prescription regarding my condition so that I can further heal myself and become CFC-free in this lifetime. All right, dr Gioti and everyone.

Speaker 1:

What I'd like to look at first is the words and the grammar and the way she worded that, because that's harming her a great deal. It's just psychoneuroimmunology, so she was diagnosed. We always use that word. We have to realize that the diagnosis is naming it and before the diagnosis you were Dr GOT. Now you're not. Now you are triple negative breast COCs. That'sot Now you're now. Now you are triple negative breast COCs. That's who you are, and your whole life is going to now change. You're going to be devoted to dealing with this thing that they've named.

Speaker 1:

But that's what a diagnosis does. It says you're not who you think you are, you're this, and you'll see that what I'm saying is not an exaggeration, because you actually spend your whole life becomes centered around that, regardless of what you're doing. That's in your mind somewhere on a constant basis. And then you start to see yourself that way, because I've had people say to me I'm a cancer patient, anything else. Are you married, do you have friends? Do you work somewhere? Are you an employee, employer? But no, you become that and remember, most of your activities are centered around that. So is your family's activities centered around this, the name of it, which actually is no help at all, which I have explained before, but anyway, so there's that.

Speaker 1:

So the diagnosis means you got it's like sorcery, you got a curse put on you, and the triple negative means that you don't have positive estrogen, you don't have, uh, estrogen receptors that can be measured. Um, progesterone, which is one of the other female hormones. Um, it also doesn't have progesterone receptors, but it does have and it doesn't have it, and it also doesn't have an expression of what they call HER2, right? So HER2, the HER system, the one through five, is the same as epidermal growth factor, but they named it HER. So you've got the second one because there's five being expressed more in these tissues and therefore they've developed an antibody that attaches to that and starts to eliminate it. So that's what it is and that's why the words are so important.

Speaker 1:

So saying that it's a triple negative is saying it doesn't have these three things. But what the implication is is because it doesn't have those three things, the HER2 positivity, the progesterone receptor that can be found 1% are all that's necessary. Or estrogen receptors 1% is all that's necessary to call it a positive estrogen receptor, progesterone receptor, because if you have that, that, then they have drugs to go after that particular thing. So the reason to determine whether or not you are triple negative or just positive, or whatever it is, is to know which products and services they can sell you, because they're working with a sales algorithm but that they most likely got from the American Society of Clinical Oncology. And yeah, now the other thing. And then your oncologist wanted to re-biopsy, in other words, do a second biopsy. I'm not surprised, but I can't think of another reason Probably wants to get it in the axilla to find out if it's the same, if it's the one and two. So that's the re-biopsy.

Speaker 1:

And and remember, you were negative for the broccas, and the broccas that become nasty thing. I don't want a brocca gene, but we all have brocca genes. What they are is double-stranded dna repair mechanisms. That's part of it, and the ability to repair it is is gone and that's why they're calling it BRCA. B-r-c-a stands for breast cancer. You know that word. So here's the thing when you target with monoclonal antibodies, because you also have some similar therapies for the estrogen receptor tamoxifen and things like that and we're giving you a drug that decreases, that decreases your amount of dastritiums in your in your blood, so uh, the uh or the uh, so you triple negative. So if you're triple positive, they could have given you those things, but because you're triple negative, they can't and they say, oh, it's, it's the worst and it's um aggressive, and they use all these words. So that's why I don't even like to use braca. Or because there's just the name of it, is it's wrong, there's, it's not a gene that's producing cfcs. That's what it sounds like, right when someone says I'm braca positive, whatever it is.

Speaker 1:

And then your pd, your pdl1, your PDL one, which is, it's the pro programmed death, ligand, ligand. And what is a ligand? A ligand is that part of a molecule that attaches to a receptor for receptor for that, so the cell attaches to the other cell by it's. It's a ligand, the getting into the receptors. That's what the word is. So it turns out that there are PD-L1, which is their PD-L1s, and there's a programmed death receptor. So there's the ligand and the receptor which block the immune system and they prevent the T cells from eliminating the tumor. So that's great.

Speaker 1:

If you can set something in and block the ability of that to happen, then that's a tremendously positive thing to do for someone Turns out that doesn't work for more than giving you a couple extra months of life, and most of the time the life that you're getting extra a couple months is not worth it, because you're sick and you're paying. It's not the kind of life that you're looking for, but anyway. But that's why they would find out that, and so that you. What's very important for you is that you get away from using these words and thinking in those terms, because even though you're not using that word, you're still saying CFCs. So you're not using the astrological sign, you're still in that same paradigm because you're using all the terminology that defines that.

Speaker 1:

All right, so that's one thing is that you had already seen a certified biological dentist who did a total evaluation of your mouth and found these two or three things that were causing a problem, like root canals or metal. There's lots of different problems that could be happening. So they not only do that, but then they treat you. In other words, they reverse that symptom or change you so that your body's no longer going through that um and uh, what was it the um? So anyway, anyway, let me get back to the brocca, because it's very important. What I'd like everyone to know is that if you're brocca one or two positive, that means either your mother or father had it, you got it All right.

Speaker 1:

So that's when it's an inherited gene defect. And what's the defective? Again, one of the enzymes that's involved in double-stranded DNA. So it's not a gene that's causing CFCs. It's a gene that would normally clean up a DNA mistake. But you got one parent Now in order for this to be a problem, because we have pairs of chromosomes.

Speaker 1:

So the something that's being produced is going to require the left and the right hand. So if you haven't done that, then you need to in order to really call this a BRCA event. So that means you need to get what they call a mutation this lifetime and that's called a somatic mutation. So in order for a BRCA1 or 2 to really manifest, you have to get very toxic this lifetime, right? So what would you do then if that were the situation? Well, you'd clean up and then eat a healthy diet and live a healthy lifestyle. And what would you do if you didn't have this diagnosis? It should be the same answer, all right, I just don't want all that to throw you off from it.

Speaker 1:

So your question is what else is there other than different ways of administering chemotherapy and high-dose vitamin C? Well, first of all, you need to be meeting your physiological requirements by taking enough of the vitamin A carotenoid group, having your vitamin C level up to a therapeutic. What's considered therapeutic? You have other. I mean, because vitamin c for ever, for so many things to make neurotransmitters, to make cortisol, uh to it's just it's involved in rewriting that epigen, epigenetic group of changes that allow the cfc to grow. It undoes that. It's incredible what it does. What's that seminar? Um, but anyway.

Speaker 1:

So by taking enough orally, which would be like two grams of sodium ascorbate liposomal four times a day, or a one liter, one quart of drinking water with eight grams of sodium ascorbate, this is all that. You'd be sipping it slowly. So the seven, because if you drink too much of it, most of it won't be used. It'll come out in your urine and the threshold is about 500 milligrams. So that's vitamin C. So if you're taking it orally and you're able to satisfy all your physiological requirements, if you had enough, you probably wouldn't be able to have ever developed CFCs because you would be turning off their epigenetic, which is kind of like their paradigm or their scaffolding that allows the cell to be turned that off right Reverse that.

Speaker 1:

The other thing a vitamin C does that I didn't mention is those spaghetti-like blood vessels that burst, meaning that oxygen is not arriving somewhere and when it doesn't, tissues become low oxygen and the medical term for that is hypoxia. When that happens it stimulates a group of events by something called HIF1-alpha, which is hypoxia-inducible factor alpha. Anyway, that causes angiogenesis, tissue proliferation etc. So vitamin C is going to quench that, because the vitamin C is necessary for the enzymes that turn that off naturally and without the vitamin C you won't be able to do that. So anyway, when you're taking enough vitamin C orally and enough of the carotenoids and you're like overdosing with vitamin d3 and you're getting an increasing amount of melatonin and you've taken care of your iodine and thyroid and your adrenals and you've done all that right then, uh, or even if you're close, that's where the intravenous would be good, because the intravenous is going to go.

Speaker 1:

Remember, it's got to get up to a certain concentration in your blood, right, 350 milligrams per deciliter, to have the desired effect of eliminating a tumor. And it's proven. This is not. And so, in order to get there, how much do you give? Well, I'm getting 75 grams a week, or every other day, or whatever, I'm getting 50.

Speaker 1:

The problem is is that most doctors, most clinicians, don't measure your fasting ascorbate level. In other words, how much is your ascorbate in your blood when you wake up in the morning? It's, it's not. It's also, um, you see, the amount we need for that to be occurring should be satisfied already because we're taking enough orally. So now when I get the IV, it won't have to fill up a deficit, it'll go straight up and I can achieve that 350 milligrams per deciliter more easily. So perhaps on 25 grams, 50 grams instead of 100 grams, but it doesn't matter because most doctors are not measuring it anyway. They're not measuring before and after the vitamin C.

Speaker 1:

Do I have the levels in my blood that are adequate to kill the tumor. Because the only benefit? Well, you get all the other benefits, but the main purpose and benefit of high-dose vitamin C IV is to get enough of it to the tumor so that it can kill the tumor. And it kills the tumor via a certain mechanism that is prevented by healthy cells because they have all the enzymes they need, but is unstoppable by cfcs because they don't have that enzyme, right? So if you're getting enough the a, like I said, which is the carotenoids, mixed carotenoids, the c, the d, uh, the melatonin, the thyroid iodine and the adrenals, and you're balancing all of those and there are other things you need to do, right, that's going to.

Speaker 1:

You know that's when the intravenous vitamin C is going to have a relevant effect. Sadly, people are going in and getting 50 or 75, whatever it is, for some other reason. They're saying well, I was able to tolerate it. I'm not sure what that means. I think it means that sometimes someone's getting some vitamin C, especially if it's in a sodium ascorbate form. The reason you want sodium ascorbate is because that's the only form in which ascorbate can be picked up by a cell. It's going to have a sodium. So if that's all satisfied, then the pro-oxidant effect can take place by giving you intravenous vitamin C. Otherwise, it won't happen and the only way you would know is by measuring, because you're not going to see it is by measuring the before and after and comparing it. Sadly, very rarely does that happen. You know what else? There's a lot. There's iodine and iodine fibroid situation, and understanding that iodine is one of the bosses of the immune system turns out to be very important.

Speaker 1:

So the next question is um, listen, oh, I guess I don't know. So it's topic is parasites. How can I get a consultation with you? I think we've talked about that. I think this question was on last week. You said I want to get a consultation with you on facebook and it fell apart. I extreme eat extremely healthy, right, you went through all that, I think. Yeah, we did talk about this this this last time. So, um, but basically I don't do individual site consultations anymore because there were way too many to even fantasize about getting close to getting them all. Um, which means it'd be so many people.

Speaker 1:

Excuse me not getting the consultation, because I was doing it for a while and if I you know, you know usually we're on for as long as we need to be could be two hours, three hours and the initial consultation. Then, even though I may never meet the person, I would have to do the initial blood imaging prescriptions, blood test prescriptions and all that, all right. So the consultation was not just that time, the two hours or whatever it was it now. Then I have to follow up because I've already recommended to get these blood tests and to get you know that. So I've got to make sure that happened. So we have at least one follow-up, right? Well, it turns out that, um, look, I've had people on there who, uh, I've been following up on for years and so I can't have to. I mean, that's all I would be doing. So it's much more efficient to do it like this, this way here. So, um, you need to please make an appointment. You should join the um parasite group.

Speaker 1:

Oh, excuse me, you're saying here my blood tests all came out okay, but you just know something's in your body, Okay, and that's a good point that you bring up. I think we discussed it last week when we talked about your situation. And when they say normal, my blood tests came out okay, that means the result on your system of your blood gave you a number. The result on your system of your blood gave you a number, a concentration of this particular element, that it falls within the normal range. Now, the normal range is the normal range of the community in which you live. That's why they're called community reference labs. But if your community is pretty sick because they're a normal average city nowadays where you know about every 50 or 60 seconds someone has a heart attack I'm not sure what the number is now and then every several seconds someone's getting a stroke, they have almost a 50% chance of having CFCs. You know 70% are getting diabetes and that's the group that you're using for reference. So you don't want to be in the middle of that. What they don't have are the healthy ranges, right. So when they say your blood test came out all right, I don't know what they mean. So you get a list of all the blood tests you should ask for and all the other really important benefits, in addition to the lives live, live streams every week, etc.

Speaker 1:

In the question and answer for on zoom, and that way you have access to you know, kind of like a, a doctor who's there virtually right because, which is always a good reason not to work with me, because you, I can be there. There's no way I can examine you and really understand who you are, so I can't really be someone's physician. But if you've consulted, what are you going to do? Consult with them and then just say, yeah, I ordered these tests, have someone else tell you what they're about, you just have to take care of them. So imagine I'm doing six at eight a day, and by now, what four or five years I've been doing this particular type of work. I mean, that would be the only. I couldn't even talk to new people. I have to just be taking care of these answers. So it's physically impossible. These groups are what's happening. So you should join the Parasite, okay.

Speaker 1:

So we talked about that last time. We talked about that too. Where is the? I can't see the date. I was just wondering if we got the wrong date. Nope, it says June 8th. So I guess the question was brought. All right. So now this is from. Wait, no, we did that, I'm sorry, I'm sorry.

Speaker 1:

So we were on Yeneti and so your blood test came out, okay, but you know there's some in your body and you eat healthy. That's what you're saying. You stay active, you don't drink or smoke, but you're just not feeling good, yeah, so basically, that's what she's saying. She's saying I recently repeated a stool test because of one year I've been having a sharp pain in my. I went to the, I was having a sharp pain in my right side and it just won't go away. So, anyway, in 2019, it all seemed to have correlated with um blastocysts in their blood. Well, that's pretty interesting if they were in your blood, uh, and they gave you antibiotics and you antibiotics, and then I ended up in the ER with blood clots near my cecum. So that's where you are now.

Speaker 1:

It sounds like, yeah, and I think we talked about this what a parasite is and all that and how to deal with it. So please look at last week's live, because it's been recorded. And then we have Rhonda live, because it's been recorded, and then we have ronda, and ronda is saying um, I have a cyst on my kidney and four gallstones. Could you suggest a protocol for me? Thank you. Well, I thought we answered all these questions anyway.

Speaker 1:

There can be cyst development in tissues. You can get ovarian cysts from a failed ovulation and you can get up. You get other systems where it's basically a fluid-filled sac and or you have to realize that one of the ways in which the protozoal parasites protect themselves, one of the ways is, uh, by getting into it and that's what a cyst turns out to be before you go any further. That's what I would do, right, and you know that involves a good, healthy, fast and cleansing. So it's not. It's not that important to find out exactly what it is and where they are although if you did, that'd be great except to realize that microorganisms don't live isolated. Even in an infection, where it's predominantly something, they're still not in isolation. So you just need to keep that in mind, and that's why going after just one thing and trying to eliminate it without supporting the whole orchestra to become tuned will never work. Will never work because it's working outside of the understanding that what needs to happen is the physiology needs to be balanced and restored right.

Speaker 1:

So I know we answered this question last time and this one oh, this is an ad Someone trying to sell themselves to me, I'm talking. That sounded weird. Um, they're offering me help with my website or something and they want me to use them. We did this one too, jeff. Oh, I don't know if we answered this, or I just read it, but this is by um k and it says colonoscopy four years ago caused major motility problems, issues, the methane gas and bloating accompanied it, all right.

Speaker 1:

So colonoscopy is, as you know, where the gastroenterologist, you know, uses something rectally to take a look fiberoptically or directly at the lining of your colon to see if there are any tumors or just polyps or what they are. All right, so that's a procedure and if the procedure did not involve biopsying, it would not be dangerous. There's chances of perforation and things, but I mean it would not be, you know, it wouldn't be as as bad so the, or is that again? So somehow what that caused was motility issues. And what she's talking about is that the way in which the food is propelled along in the gut is called peristalsis and that just means that because, remember, the lining of the gut has smooth muscle around it which contracts, but it contracts in a sequence so that we actually have movement and that's how things move around. So the more anxious you are, the more in sympathetic drive, the less you're going to be able to use that. And there are many different ways we can do to stimulate our vagus, which means to restore the peristaltic function, because you know, without a good peristalsis, you're going to become very constipated because you've got to get things moving All right.

Speaker 1:

So what you're asking is where was that all right so? So let's go back. So you'd always, uh, you had the colonoscopy. It caused the motility issues. Then you got then the methane gas production and bloating. So that's one of the gases that's produced by microorganisms that are not really, uh, the ones you want to have in your gut to help you digest. And you'd always been like clockworks, have big, regular bowel movements. I know we answered this and so we went into colonics and when you should do them and all that. And that's the question.

Speaker 1:

And the other thing I mentioned I, I hope you remember is that, since, if it's true that you have trouble with peristalsis, um, you know a good, thorough cleanse and allowing your body to rest, and then doing you know different therapies like yoga, tai chi, qigong, meditation. You know all these things can stimulate the parasympathetic system, which is the one that's going to cause the peristalsis to work, and then the other thing that utilizes the autonomic nervous system, which is the sympathetic and parasympathetic fear or anxiety, and all that stuff that stimulates the adrenal glands, okay. So we want to uh herbs, okay. So how do you do a cleanse? How do you do a cleanse and all that stuff? I think we talked about that. You know, you can do a juice cleanse and then you can do the fasting and all that sort of thing and and then, um, whether or not you're sure you have parasites or not, it's always good to do parasite cleanse because we're being exposed to it and our immune systems have been greatly compromised from what they were in 1900, which I never finished saying that. But basically in 1900, we only had the ambient EMF, and now we've got such high exposure to electromagnetic frequencies and the lower frequencies, both which are harmful frequencies, and the, the lower frequencies, both which are harmful um, we've got amounts to which our body is having a very difficult time dealing with and we're seeing immunosuppression in almost everybody, whether or not they have cfcs. So, yeah, I would uh, yeah, so I I said anyway that the doing a parasite cleanse it means it's part of a total cleanse. You can't just think I'm doing a parasite cleanse means it's part of a total cleanse. You can't just think I'm doing a parasite cleanse because they live in a certain environment, so it's good to do a juicing cleanse, maybe even a water cleanse. You don't have to Colonics, lymphatics and all that stuff and then do the anti-parasitic protocol. But now if you say you had a specific problem and you found it and you know that's what it is, then you don't have to. You still have to do that, but you can get started with some other, the anti-parasitics you know, while you're going through detoxification processes, and if it's in the form that yours is so, then you want to make sure that you've got the right anti-parasitics, because there's different forms and different kinds. I know we talked about that one. Well, we talked about all these. And here's Mary Jean, we talked about that. And Christy, we talked about that. Wait, where are the new ones? Oh, here they are.

Speaker 1:

Gosh, here's a question from Parkinson's, and this is from Hannah and she says hello, parkinson's, diagnosis 2024, 64-year-old male not taking the prescription medication and following a protocol juice detoxing with IV vitamins. What is your recommendations for this condition and the best way to follow it? Well, with Parkinson's, I don't know if you know, but there's actually damage to the, uh, a certain part of the brain that results in a fine tremor and at rest and you wind up actually getting us your face the muscles don't move like that some cognitive decline shuffling when you walk, you know. So that you know pretty specific and that's called Parkinson's and, since it's in that area, called the substantia nigra, and we know, then we can deal with it right and what we want to do is allow those cells to make as much dopamine as they need. So how do we do that? Well, first of all we we need to understand that we're, we're really not um, when we call parkinson's and then we call I'm talking about neurodegenerative conditions, parkinson's, ls, ms alzheimer's, all that stuff. We give them names, them names, but basically there's a whole variety of, there's a whole lot of cognitive decline and neurodegeneration going on, and especially now with these extra EMF and microwave EMF and all that and to name it something specific. Well, it gives them a name and it gives treatments, members, the sales protocol, but it can fluctuate between looking like this and looking like something else.

Speaker 1:

I had a. I had a woman years ago who had gotten a flu shot and then, you know, she got to the point where she wasn't able to flow Right and she was diagnosed with ALS and then it went away. Als doesn't go away. It usually it goes on to become a terminal. It's where all your muscles are stopping and finally the muscles of your respiration, so you can't breathe. So yeah, but she went to not having it, which doesn't happen. Then she got another flu shot the next year and now it happened, and then it happened permanently. So what I'm saying is what they're calling ALS is because it met certain criteria, but there's no thing called ALS, there's no thing called Parkinson's. That's my point.

Speaker 1:

But it turns out that glutathione, which is what the cells of the substantia nigra in the brain with people with Parkinson's cannot produce. You want to be able to enhance that. So that's a very important part of the program. So if you could enhance the production of the glutathione or give the glutathione, then that would be helpful. And what we found was actually giving intravenous glutathione which, would you know, obviously intravenous is going to get to the substantia nigra and it's going to decrease those symptoms that are occurring from it. So the glutathione was very helpful. And so people would walk in with very severe Parkinson's symptoms you know the shuffling gate and all that stuff and giving them the intravenous glutathione, they actually went away and they could now talk naturally, and the problem was it didn't last that long and so we came up with glutathione. It actually went away and they could now talk naturally. And the problem was it didn't last that long and so we came up with glutathione suppositories and that was hard to get levels and all that sort of thing.

Speaker 1:

And then if you look at the ways of you know what are the biochemically, what do you have to do with the body to improve its ability to make glutathione? And there's lots of ways of doing that, which include diet etc. And, um, anyway, so that's kind of you know where I would work with parkinson's. The other thing is, I would you have to detox because, remember, the reason that came about is because of a toxic insult, and what has been found with particularly the the uh, when you actually damage cells in the substantia nigra uh, is pesticides. They seem to target that and so people that had pesticide exposure, et cetera. So by eliminating and detoxifying the, the, the uh, your body and getting rid of the parasites and then upregulating your, your ability to cleanse in your liver. But there's ways of doing that. So there's a lot to that.

Speaker 1:

Um, because once you start anti-anti-parkinson's medication, it kind of snowballs and then you need it. So, uh, and they become less and less effective. So it's really good if you, if you have Parkinson's, to delay the onset of treatment, and you can do that forever, if you can just restore the ability to do that. So, anyway, but that's occurring to everywhere, especially in cities with a lot of 5G. That we're seeing is like the woman who got with the flu shots is not necessarily that particular process I was just talking about, you know.

Speaker 1:

So when they say, well, you've got something that looks like ALS, but it could be Parkinson's or it could be multiple sclerosis and stuff like that, what they're saying is that you've got a derangement, you've got to imbalance, a toxicity of your nervous system is what they're saying. System is what they're saying. However, um, and and and. If you give it any particular name, that doesn't matter really, because there's no treatment for als, there's no real treatment for ms and there's no real treatment for Parkinson's. So I don't know why they're so concerned about naming it. Oh, I know why because they have specific drugs that don't work. But anyway, the point is it's neurodegeneration and it can have many manifestations, right, right, and when we see it in young kids, it's autism, and these names only give a justification for using a certain drug.

Speaker 1:

Drugs, I'm serious, that's what it is. So, instead of doing that, you say, okay, in general, I'm going to get all the toxins out. I'm going to do chelation. I'm going to improve get all my nutrients up my vitamin C. I'm going to get all the toxins out. I'm going to do chelation, I'm going to improve get all my uh nutrients up, my vitamin c. You know you're going to do all that. You're going to restore balance and physiology right, and that'll do it. And one of the one of the benefits or effects or consequences of having a balanced uh physiology is your glutathione, your ability to produce glutathione, like you know. So we're talking about the Parkinson's, what's called Parkinson's, all right. So that's really what we need to understand.

Speaker 1:

And the point here that is very important is that why are we looking for a name? Because I know we all want it. You're saying I need a diagnosis, I want to get a diagnosis're saying I need a diagnosis, I want to get a diagnosis, I finally got a diagnosis. Well, we're trying to name, uh, put a specific name on something. For what reason? Because, implicitly, what we've been taught by the rockefellers is that if we have a, if we can give the more specific of a name we can give it, then we'll have specific medications, and if that were true, it'd be great, but that's not what's happening. We don't see the benefit all right like that. In certain cases we do, such as a pneumonia, and we give antibiotics and we see it go away. That would work all right. However, there's a lot of other things that would go into that and I didn't.

Speaker 1:

I didn't talk about that when we're answering the pneumonia um, uh question that you need to restore your health, um, and good vitamin c levels and all that sort of thing. So actually, the pneumonia can't happen in the first place, but anyway, anyway. So if you take a look at everything we're talking about, it's really the same fundamental process going on. There's an accumulation of toxins and they could be, you know, specifically accumulating in a certain area, causing a problem there, whatever, but it is toxicity and it needs to be removed. And when the toxicity is removed and you're supplying the nutrients that allow physiology to function, then there aren't any problems.

Speaker 1:

There's no need for adaptive strategies right On your body's part, right, because the adaptive strategy on your body that your body goes through is what we're calling the diseases, right. So the adaptive strategy of a cell to become insulin resistant, to protect itself from glucose, we're calling diabetes, et cetera, et cetera. You know the chronically fermenting cells we're calling. So these are adaptive strategies, physiological, homeostatic, corrective responses, and what we need to do is get rid of anything blocking that and support and give everything the body needs to not to be satisfied, and then there's no need for adaptation, so there's no problem. So I know this. You might be thinking that's not relevant to me, but it is. It's, it is, it's, that's, it's, that's what it is. It's all about that.

Speaker 1:

There was a book by John Tilden and I just happen to have it here 1915, if you can see that Toxemia Explained and basically he goes through that. But understand that in 1915, their vocabulary was different than ours because they hadn't given names to aspects of physiology that we have done now. So, discussion of a condition or a disease, it's going to be very different than that, but what he does is show you that it's basically the same thing. So even aging, right. So as you get older and you've got accumulated toxins, when those toxins actually start to impair because if you have enough toxins in any organ, it'll impair its ability to function. Well, when you've got the toxins, in particular thyroid and all your different organs, all your glands that are producing hormones, and you start to see hormone decline, then you start to see the phenomenon that we call aging. So you can imagine, if you did not, if you're, if you never had a hormone decline, you wouldn't see it, right? I mean, that's amazing. So even you know. So what I'm saying is that, if that, that can happen more quickly.

Speaker 1:

And why do I say that? Because we've got in different parts of the world, we have people delivering children at 65 and the other going, going into menopause is early, like that's 35, right, and that's because they're we're told by the medical profession and there's a million reasons why I said that doesn't even make sense. But no, it was. It was. The difference wasn't there? Both their toxicity exposure and their ability to eliminate it, right, right, and that's it. So we live a life where we're not producing, we're not exposing ourselves to toxins and we're supporting all the nutrients and all that. So that's basically it. Again, I'm sorry, but earlier I couldn't get things working. I'll get them working better someday. And sawadika, aloha, namaste, and stay healthy. Here we go. What are we doing here? We're going to do that. There we go. Cool Whatever.

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