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Study says Intermittent fasting can starve cancer cells pushing them into cell death. இன்பநிதிக்கு கக்கா கழுவும் உனக்கு எதுக்கு டா இந்த அறிவியல் பேச்சு மடப்பயலே.😂 #Annamalai

27,169 görüntüleme • 7 ay önce •via X (Twitter)

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The Dangerous Cult of 'Fasting' Influencers. Fasting has its anecdotal benefits, yes. But it is overrated. And water fasting is highly overrated. But this video featuring a Cardiologist is amusingly nonsense. There is no study from Boston (from a "University?" - how vague!) that says 7-days water fasting reduces risk of cancer (what cancer?) by 70%. And there is no proof that fasting kills cancer cells in humans. Here is what fasting does to cancers in humans. Nothing. Fasting is now become a sort of religion-like cult for wellness influencers to rake in views and engagement. From a scientific standpoint, there are no realistically good human studies to prove anything from fasting that benefits cancers. I know, I know, "autophagy" and all that. Autophagy: Autophagy is the natural, conserved degradation of the cell that removes unnecessary or dysfunctional components. Yes, its a legit term and all. But in the context of cancer reduction and fasting in humans, it sounds like "immunity boosting," another wellness fraud term. The effects of fasting on cancer cells are all based on MOUSE studies, and none explicitly translated to humans. See this paper: everything is based on cells and tissues and small animal experiments: "While research on the subject is tantalizing, there’s little clinical evidence involving humans to substantiate the claims. Studies on the potential impacts on cancer treatment from various forms of fasting or calorie restriction, including the possibility that they reduce side effects, have been limited." "Fasting may not be appropriate for malnourished individuals or those with cancer cachexia, which results in a continuing loss of skeletal muscle mass, or for people with chronic diseases. Those with diabetes need to be very careful, because of the risk of hypoglycemia." "Based on our systematic review and meta-analysis, there is currently no evidence supporting the superiority of therapeutic fasting over non-fasting in preventing chemotherapy toxicity." - see here: Even intermittent fasting (IF) is overrated in cancer. "IF may be considered in adults seeking cancer-prevention benefits through means of weight management, butwhether IF itself affects cancer-related metabolic and molecular pathways remains unanswered. See here: Also this: "Fasting for short periods does not have any beneficial effect on the quality of life of cancer patients during treatment. Evidence on fasting regimes reducing side effects and toxicities of chemotherapy is missing." See here: The whole aspect of "fasting reducing cancer incidence" in the real world is just due to weight loss. Obesity is associated with at least 13 types of cancers and reversing obesity reduces risk of cancer - nothing to do with fasting killing off cancers cells in the body. And one can lose weight even without fasting. See here: Everything from prevention of adverse events of cancer, to reduction in side effects from chemotherapy, to slowing cancer growth by reducing glucose levels, to promoting cell regeneration by affecting autophagy is all LAB BASED MOLECULAR LEVEL HYPOTHESIS that has not been proven conclusively in humans. See here: Cancer patients must not starve. They must remain hydrated and they must eat a well balanced diet because cancer condition is highly demanding. And dont water fast for 7 days. Easy for people to make reels on it, but in real life, it may prove disastrous. Water fast does make you lose weight (because of starvation) but it is not at all a healthy way to lose weight. Stop with this fasting and cancer madness already.

TheLiverDoc™

269,502 görüntüleme • 2 yıl önce

Can people in power/ authority kindly stop with this absolute BS on "fasting killing cancer cells" and citing religious nonsense to appeal to peoples emotions? Fasting is really quite dangerous for cancer patients in real life. Let me explain and bury this myth once and for all, especially for science illiterates like this guy. [1] The most common argument is that fasting "starves" cancer by cutting off its sugar (glucose) supply. While it is true that cancer cells consume vast amounts of glucose, they are biologically aggressive survivalists. If you stop eating, your body eventually switches to burning fat and breaking down muscle for energy. Cancer cells are highly adaptable; when glucose is low, many types of cancer can mutate to feed on other fuel sources, such as lactate, amino acids (from your muscles), or fatty acids. You cannot simply "starve" a tumor without starving the patient first. [2] Fasting is dangerous for cancer patients because of cancer cachexia - a wasting syndrome where the body loses muscle and fat rapidly. Cachexia is responsible for up to 30% of cancer deaths. Cancer puts the body in a hyper-metabolic state (burning energy fast). If a patient fasts, they risk accelerating muscle loss and weakening their immune system. A weak body cannot tolerate life-saving treatments like chemotherapy or radiation, nor can it fight off infections. [3] Most claims about fasting curing cancer come from studies on mice or cells in a petri dish. In a dish: You can kill cancer cells with almost anything (lemon juice, bleach, starvation, even shooting a bullet at it at close point or using a grenade to destroy the entire lab) because they have no immune system or body to protect them. In a human: The biology is infinitely more complex. Human metabolism, hormonal fluctuations, and tumor micro-environments mean that what shrinks a tumor in a mouse often fails completely in human trials. [4] Proponents often cite "autophagy" (the body's cellular recycling process triggered by fasting) as the cure. They claim it cleans out cancerous cells. Science shows that autophagy is a double-edged sword. -In all people, autophagy is a normal physiological process - whether fasting or not, which help in cleaning up damaged cells. -But in patients with cancer, once a tumor exists, cancer cells can actually hijack autophagy to survive stress (like chemotherapy) and repair themselves. In this context, fasting could theoretically help the cancer survive the treatment intended to kill it. [5] "Cancer" is not one disease; it is over 200 different diseases characterized by uncontrolled cell growth. Some cancers are driven by hormones, some by genetic mutations, and some by viruses. A fasting protocol that slows down one specific type of breast cancer might have zero effect on pancreatic cancer, or worse, accelerate a different type. The most lethal aspect of this misinformation is the delay in treatment. Cancer is a time-sensitive disease. While a patient spends months trying to fast the cancer away based on religious or alternative advice, the cancer often metastasizes (spreads) to other organs. Once cancer spreads, it often moves from being curable to being terminal. Relying solely on fasting wastes the critical window where medical intervention could have saved a life. Suggesting a single "ancient cure" for 200 complex genetic diseases is scientifically illogical... ...and generally stupid, as this video proves.

TheLiverDoc™

193,312 görüntüleme • 7 ay önce

74% Of Doctors Would Refuse Chemotherapy For Their Own Cancer Treatment & Would Instead Use Alternative Real Cancer Cures For Themselves. Doctors Cite Chemotherapy As Unacceptably Cytotoxic & The 5 Year Survival Rate Is Only 2.1% Yet, Doctors Push Chemo Onto Their Own Patients. In the MacKillop et al study, only 17% of medical oncologists said that they would take chemotherapy for painful bone metastases & spine cancer. Even with modern chemotherapy, less than 30% of medical oncologists & oncology nurses would take chemotherapy. Cited in "The contribution of cytotoxic chemotherapy to 5-year survival in adult malignancies"... The overall contribution of curative & adjuvant cytotoxic chemotherapy to 5-year survival in adults is only 2.3% in Australia & 2.1% in the USA. Chemotherapy is incredibly toxic & must be handled in the clinical setting as a biohazard. Medical professionals who handle its contents in a hospital setting must wear protective gear for personal protection from the poisonous features of chemotherapy liquids. Chemotherapy came from one of the cruelest weapons ever invented as it was a weapon of war called Mustard Gas. Mustard Gas was banned in 1925 for being used as a weapon of war, citing it's deadly harm & inhumane use against war enemies. After that, researchers found it destroyed bone marrow & lymphatic tissue & decided to market it as a drug for profit. The 1st chemotherapy drug was Mechlorethamine Hydrochloride (HN2), which is a Nitrogen Mustard. Currently, 5 Nitrogen Mustards are used in Chemotherapy including Mechlorethamine, Cyclophosphamide, Ifosfamide, Melphalan & Chlorambucil. Chemotherapy is not the answer for healing the body from cancer. Scientists Have Known Since the 1930s That Fasting Starves Cancer Cells… So Why Is It Ignored? 🤔 Dr. Otto Warburg (Nobel Prize winner) discovered that cancer cells thrive on glucose (sugar). He found that cancer cells have a damaged metabolism, meaning they rely almost entirely on fermenting sugar for energy—unlike healthy cells, which can switch to fat or ketones. ✅ Fasting drops blood sugar & insulin levels – Starving cancer of its preferred fuel. ✅ Increases ketones – Cancer cells cannot use ketones for energy & thus starve & die off. ✅ Triggers autophagy – The body removes damaged cells, including pre-cancerous ones. ✅ Boosts immune function – Fasting increases white blood cell regeneration, helping fight disease. 🚨 So why don’t doctors recommend fasting? Cancer treatment is a multi-billion dollar industry. Most oncologists don’t study nutrition or metabolic therapy. The system profits more from lifelong chemo & radiation patients than a free, natural intervention. Meanwhile, studies show fasting + a ketogenic diet slows tumor growth, shrinks tumors & makes complete remission possible. But instead of researching this further, mainstream medicine pushes drugs & expensive treatments. Dr William Makis & Dr Paul Marik, along with many leading physicians & oncologists have developed a groundbreaking protocol entitled: 'Targeting the Mitochondrial-Stem Cell Connection in Cancer Treatment: A Hybrid Orthomolecular Protocol' which involves a thorough step by step protocol of fasting & eliminating all glucose from the diet, while using ivermectin, fenbendazole & supportive nutrients & lifestyle changes for cancer treatment into remission. ⏩ ⏪ 👇Oncologists Would Not Choose Chemotherapy👇 👇5 Year Survival On Cancer Malignancies Chemo👇 👇Dr Thomas Seyfried: Cancer Metabolic Disease👇 Speaker: Dr Eric Berg

Valerie Anne Smith

285,849 görüntüleme • 11 ay önce

"Biopsies Spread Cancer...Biopsies Are The Kiss Of Death. The Needle Punches A Hole In The Tumor, Dragging Cancer Cells & Spreading Them." Dr Ben Johnson Doctors Finally Admit That The Very Test Being Pushed On Patients Is Causing Cancer To Metastasize All Throughout The Body. The body self-contains a tumor within a fibrin sheath. A needle biopsy breaks the seal of the tumor that kept it contained & allows the pathogenic toxins &/or parasites to be unleashed. When a hornet's nest is poked, it doesn't calm the hive...it angers & scatters. That’s what happens when a needle pierces a tumor. Cancer cells are dragged into new territory, inflammation flares, the immune system gets distracted, and the “nest” gets angrier. Cells are dragged along the needle tract. Local inflammation activates tumor growth. The immune system is suppressed & cancer cells invade tissue, blood & lymph. Biopsies trigger metastasis, inflammation & tumor seeding: "Biopsy of primary tumors resulted in significantly increased incidence & number of lung metastasis."(PMID 25061543) "Biopsies promote intraperitoneal tumor dissemination & progression." (PMID 23258276) "Core needle biopsy of breast tumors increases distant metastases. (PMID 25425969) "Biopsies lead to tumor cell dissemination & seeding of malignant tumors." (PMID 22686607) "Human breast cancer biopsies enhance adjacent cancer cell proliferation." (PMID 27249999) Top Doctors Are Now Admitting 'That Standard Of Care' Is Killing Patients: "Manipulation of an intact tumor...is associated with an increase in the incidence of sentinel node metastasis." (John Wayne Cancer Institute 2022) "Cutting out a section...endangered the person's life by aggravating the malignant growth." (Dr Perry Nichols) "Biopsies spread early cancers." (Dr Jonathan Wright) "Biopsies introduce cancer cells into the bloodstream." (Dr Leonard Gomella) "Biopsies cause cancer cells to spread & the risk is higher in certain types of cancers like prostate & kidney cancers." (Dr Hal Schofield) "Biopsies cause cancer to disseminate further into the body & this has serious implications to patient outcomes." (Dr Robert Nagourney) Alternative Tests That Do Not Disturb Fibrin Sheath Of The Encapsulated Tumor: 1⃣ Multiparametric MRI (pmMRI): Non-invasive. No ionizing radiation. Detects structure & function in high resolution. 2⃣ Color Doppler Ultrasound: Maps tumor blood flow in real time. No radiation. No compression damage. 3⃣ Liquid Biopsy (ctDNA /CTC Testing): Blood test for cancer DNA or cells. No mechanical disruption of tumors. 4⃣ Thermography: Non-radiation, non-invasive technique that uses infrared cameras to detect heat patterns in tumors. Information is anti-fear. Knowledge is power. It gives you choices. It gives you power. If you’ve been diagnosed, please don’t rush. Research. Ask questions. Trust your intuition. Sometimes slowing down is the most urgent thing you can do. The cancer industrial complex is a powerful profit model & needs a massive overhaul. Too many patients blindly walk into these procedures without informed consent, never being told the risks. You can choose to not disturb the tumor at all & instead implement a protocol to shrink & enable the body to eradicate the tumor all together. Many cases of cancer tumors are actually parasitic eggs sacs misdiagnosed as cancer. There are ways to diagnose cancer without the risk of spread & acceleration. And ways to prevent & treat cancer without the harm of Chemotherapy & Radiation. There is a groundbreaking protocol by Dr William Makis, Dr Paul Marik & others that uses Ivermectin, Fenbendazole, Methylene Blue, Fasting, Ketogenic Diet & other proven cancer remission strategies that addresses cancer & parasites simultaneously. ⏩ ⏪ 👇Seeding Tumor Cells Into Metastasis👇 👇Needle Biopsy Promotes Metastasis👇 👇Needle Biopsy Accelerates Cancer👇 Speaker: Justin Stellman

Valerie Anne Smith

770,354 görüntüleme • 11 ay önce

"One Of The Most Powerful Ways To Stimulate A Healing Response In The Body...Is To Stop Eating." Barbara O'Neill Fasting Is Like Deep Cleaning Your Home, It Allows You To Eliminate The Rubbish. Before Restoration & Regeneration Can Happen, Every Room Needs To Be Cleared. Fasting allows your body to enter into the state of Autophagy...the body's way of cleaning out damaged cells, in order to regenerate new healthy cells. Autophagy plays a critical role during cellular development & differentiation, functions in tumor suppression, & linked to life span extension. Autophagy also has diverse roles in innate & adaptive immunity, such as resistance to pathogen invasion. Autophagy has many benefits, including: Cellular homeostasis: Autophagy maintains the balance of cell parts, preventing damaged parts from building up & slowing down cell function. Aging: Autophagy prevents cells from deteriorating prematurely, which contributes to aging. Energy production: Autophagy converts nutrients into energy & mobilize energy stores like glucose, amino acids & nucleic acids. Defense against pathogens: Autophagy eliminates pathogens like viruses & bacteria. Protection against neurodegenerative diseases: Autophagy prevents & also treats neurodegenerative diseases like Alzheimer's & Parkinson's Disease. Protection against cancer: Autophagy prevents tumors by eliminating toxic substances. Protection against inflammation: Autophagy protects against inflammation & increases the ratio of Bacteroidetes to Firmicutes in your gut microbiome. Reduced oxidative stress: Autophagy reduces damage to cells caused by free radicals & reduces your risk of developing heart disease, metabolic syndrome & cancer. Improved DNA stability: Autophagy keeps DNA & genes stable. Improved blood sugar control: Autophagy maintains blood glucose homeostasis & combined with carbohydrate restriction, puts type 2 diabetes into remission. Improved neuronal health: Autophagy supports neurogenesis & neuronal development & increases your energy levels by burning fat instead of glucose for energy. Intermittent & extended fasting is crucial for healing every condition & ailment. Breaking the fast with nutrient dense healing & rebuilding foods like bone broth, beef, eggs & butter give the body the fatty acids & bioavailable amino acids for refueling. 👇Short Term Fasting For Autophagy Healing👇 👇Beneficial Autophagic Response👇 👇Molecular Mechanism Of Autophagy👇 Speaker: Barbara O'Neill Video: Health 1 Solutions

Valerie Anne Smith

29,550 görüntüleme • 1 yıl önce

Oncologist Dr. William Makis: "The turbo cancers after the COVID vaccines do respond to the antiparasitics, and they respond very well... [And] why do these antiparasitics work?" Todd Callender: "Cancer's a parasite?" Makis: "That's one possibility." This clip of Dr. Makis (William Makis), a radiologist, oncologist, and cancer researcher, is taken from an interview with attorney Todd Callender posted to the VaxxCHOICE (VaxxCHOICE) Rumble channel on November 21, 2025. ---------------Partial transcription of clip---------------- Dr. Makis: "The turbo cancers after the COVID vaccines do respond to the antiparasitics and they respond very well. This is, you know, whether it's ivermectin, fenbendazole or mebendazole, these patients are responding. "Now this is very important because patients who've developed cancer after taking Covid vaccines, they don't respond usually to conventional treatments. That's one of the hallmarks of turbo cancer is they present at a very late stage. These are extremely rapidly growing tumors. They're coming in at stage four. And it's whether it's young women with breast cancer, women in their 20s, something we've never seen before, young women with, men and women with colon cancer in their 20s and 30s. "Again, we've never seen—" Callender: "Two- year-olds, I've heard of two- year-olds with colon cancer—" Dr. Makis: "—we've never seen this before. That's the incredible part. And they're not responding to conventional treatments. So, they're not responding to chemo, they're not responding to radiation therapy, immunotherapy, or if they do response, they have a very, very short response time or remission time. And then the cancer comes roaring back. "And in a lot of these tragic cases, the patient dies within six months. This is another one of the features of turbo cancer is the prognosis is extremely poor if you go the conventional route. So you need something else. Now when you're using antiparasitics, for cancer, the dose is higher than the dose you would use to treat parasites or to treat Covid. So I give just a rule of thumb for ivermectin, for example, it's about five times the dose that you would need for cancer, about 5 to 10 times the dose than if you were just treating parasites or viruses. "And to go into the— why does it work? Why do these antiparasitics work?" Callender: "Cancer's a parasite?" Dr. Makis: "Well, that's one possibility. But there's more to it than that because, out of the 400 papers that have been published, a lot of those researchers look at the mechanisms. They are trying to identify the mechanisms of how ivermectin is treating these cancers. "And you've got, for example, there was one study published a few years ago, Mexican researchers, again, you're not going to see this done in the United States, Mexico. Mexican researchers took 28 different cancer cell lines, applied ivermectin to them, and all of them responded. Now to various degrees, you had breast cancer and ovarian cancer actually responding the most to ivermectin. You had the most cancer cell killing when they were exposed to ivermectin. "But when they look at the mechanisms, they've identified a number of interesting things. For example, ivermectin shuts down and kills cancer stem cells. Now, this is important because cancer stem cells are the reason chemotherapy doesn't work. When you have stage four pancreatic cancer, stage four ovarian cancer, and you go to your oncologist, they will tell you, we will give you chemo, but we can't cure you. It's palliative chemo. It'll buy you an extra six months, an extra 12 months of life. "The reason why they say that is why the chemo is palliative, not curative. It's is because chemo cannot kill cancer stem cells, which are not rapidly dividing. Chemo will kill everything that's rapidly dividing, but cancer stem cells are not rapidly dividing. And so the chemo will kill the rapidly dividing tumor cells, and it'll leave the cancer stem cells alone, while the cancer stem cells will start rapidly dividing a year later, two years later, they're going to spread to other parts of the body. Suddenly you've got recurrence, you've got metastases. Ivermectin will shut down and kill cancer stem cells. "So imagine you, added to your chemo regimen, and now you've essentially turned what's palliative chemo or a palliative situation to potentially a curative situation. And I really do believe I've come to the point, having helped over 7,000 cancer patients in the last year, I've come to the point where I could confidently say that stage 4 pancreatic cancer is curable, stage 4 ovarian cancer is curable, stage 4 colon cancer, lung cancer. These cancers are curable. I think if you add repurposed drugs, you add antiparasitics, you can turn these into curable situations. "Now, of course, we have to prove that. We have to do the research, do the publications. But in the meantime, I say stage 4 cancer patients don't have 10 years to wait for mainstream oncology or mainstream medicine to catch up with what we're seeing already clinically, in practice."

Sense Receptor

96,616 görüntüleme • 8 ay önce

Dr. Sucharit Bhakdi, a renowned microbiologist and immunologist, is issuing a dire warning to humanity about the dangers of mRNA vaccines. He claims that the integration of foreign genes into human chromosomes through these vaccines poses catastrophic risks—not only to individuals but to future generations. According to Dr. Bhakdi, the introduction of bacterial plasmids and foreign DNA into human cells via mRNA vaccines is a reckless experiment that could lead to permanent genetic alterations. "Any foreign gene integrated into your chromosome can trigger cancer immediately, cause widespread cellular dysfunction, and be passed down to your offspring," Dr. Bhakdi warns. He emphasizes that once these genetic changes occur, they are irreversible, transforming the very blueprint of human biology. Every cell altered by these foreign genes, he argues, is "doomed," setting the stage for unpredictable and potentially devastating health consequences. Dr. Bhakdi asserts that global health authorities like the WHO, CDC, and FDA are pushing these vaccines without fully acknowledging their risks. He points to the presence of bacterial-derived plasmids in mRNA vaccines, which he claims can infiltrate human cells and wreak havoc on genetic stability. This, he says, is not a theoretical concern but a reality already unfolding with the rollout of these vaccines worldwide. This is not a message of fear but a call to awareness. Dr. Bhakdi urges people to question the narrative, demand transparency, and protect their health and future generations from what he describes as a dangerous overreach by global health institutions. "We are at a crossroads," he declares. "The genetic integrity of humanity is at stake."

Camus

56,578 görüntüleme • 1 yıl önce

Dr. Ryan Cole Issues Grave Warning: Mechanistic Link Between mRNA Vaccines and Cancer Formation Explained The alarming rise in aggressive cancers post-pandemic is no longer a mere statistical anomaly. It is a phenomenon with a plausible biological explanation, rooted in the fundamental mechanics of the immune system and the unique properties of mRNA COVID-19 vaccines. According to renowned clinical pathologist and immunologist, Dr. Ryan Cole, the issue is not one of simple coincidence but of direct mechanistic interference. The body’s sophisticated defense network is being suppressed and reprogrammed, creating a permissive environment for the initiation and proliferation of cancerous cells. Here is a breakdown of the mechanisms at play, as explained by Dr. Cole: 1. The Suppression of the Body’s "Marines" At any given moment, the human body circulates approximately 30 billion T-cells. This army includes "killer" cells whose sole purpose is to identify and destroy pathogenic invaders and, critically, atypical or cancerous cells. These cells, along with macrophages and dendritic cells, act as a constant surveillance unit, patrolling the body to clear threats. Dr. Cole states that post-vaccination, there is a significant suppression of these critical immune cell lines. The very technology designed to evoke an immune response initially suppresses it, crippling the front-line defenses that would normally identify and eliminate pre-cancerous cells before they can form tumors. 2. The Stealth Technology: Pseudouridine and Immune Evasion The core of the issue lies in the synthetic design of the mRNA shot. Natural mRNA is quickly recognized and broken down by the body. To circumvent this, vaccine manufacturers modified the RNA code by incorporating pseudouridine. "This is not natural," Dr. Cole emphasizes. "This synthetic sequence is packaged in a lipid nanoparticle and deliberately engineered to evade the immune system. Your body doesn't immediately recognize it as a threat, which is a form of initial immune suppression." This evasion allows the synthetic mRNA to hijack the body's own cells, turning them into factories that mass-produce the SARS-CoV-2 spike protein. 3. Persistent Antigen Production and Circulating Spike Unlike natural mRNA, which degrades in minutes to hours, peer-reviewed research from institutions like Stanford University (Dr. Röltgen et al.) has demonstrated that the synthetic mRNA from vaccines persists in lymph nodes for at least 60 days. The duration beyond that is unknown, as studies stopped there. This means the body is forced to continuously produce the spike protein for an extended, unnatural period. Furthermore, the spike protein does not remain localized; it cleaves off from the cells and enters systemic circulation, creating a constant state of inflammatory stress and immune activation. 4. The Critical Downregulation of Toll-like Receptors (TLRs) Perhaps one of the most concerning mechanisms is the impact on the body's signaling system. Toll-like Receptors (TLRs) are like the "toll roads" of the immune system—they are pattern recognition receptors that alert the body to different types of threats and orchestrate the appropriate defensive response. Citing a pivotal study from the Netherlands by Dr. Fassa, Dr. Cole highlights that the mRNA vaccine leads to the downregulation of key TLRs, specifically numbers 3, 4, 7, and 8. "This is devastating," he explains. "TLRs 7 and 8 are crucial for antiviral defense. But the suppression of TLRs 3 and 4 is directly associated with cancer pathogenesis. When you see a dropout of these receptors, you see a loss of immune surveillance against tumors." Aggressive breast cancers, prostate cancers, and leukemias are frequently found to have downregulated these specific Toll-like receptors. The vaccine appears to be inducing a biological state that mimics the immunosuppressed environment seen in these cancers. 5. Additional Pathways to Mutagenesis The cascade of dysfunction does not end there. The pseudouridine modification has also been shown to disrupt vital cellular communication pathways, including: - Protein Kinase Pathways: Essential for regulating cell growth, division, and survival. - Retinoic Acid Receptor Pathways: Critical for cell differentiation and apoptosis (programmed cell death). Disruption in these pathways can lead to uncontrolled cell proliferation and impaired ability to clear damaged cells—hallmarks of cancer initiation. Conclusion: A Perfect Storm for Oncogenesis Dr. Ryan Cole concludes that we are witnessing a "perfect storm" created by these interventions. The synthetic mRNA and lipid nanoparticles trigger a multi-faceted assault on immune competence: - Suppression of killer T-cells and natural killer cells. - Persistent production of an inflammatory antigen (spike protein). - Downregulation of critical cancer-fighting Toll-like Receptors. - Disruption of core cellular signaling and regulatory pathways. The result is a body less capable of performing its constant, natural duty of cancer surveillance and destruction. This is not speculation; it is a mechanistic explanation based on emerging science for the troubling oncological trends being observed globally. The claim demands urgent, independent investigation free from political or commercial influence.

Camus

67,994 görüntüleme • 1 yıl önce

5G APOCALYPSE: THE EXTINCTION EVENT Full Documentary This film exposes the 5G threat. Featured in this film are weapons development experts, biologists, molecular & cellular biologists, blood microscopists, activists, as well as others on the frontline. Further research 👇 The Influence of Being Physically Near to a Cell Phone Transmission Mast on the Incidence of Cancer 5G Radiation Causes ‘Microwave Syndrome’ Symptoms, Study Finds 5G REMOTE KILL VECTOR: Science paper reveals cell phone signals can activate the release of biological PAYLOADS from graphene oxide injected into the body 5G is dangerous and will harm every living being 5G Health Risks: How Much Exposure Can Humans Withstand? 5G Health Risks; The War Between Technology and Human Beings 5G Danger: 4 Ways 5G wireless technology can seriously harm human health How the Soviets Weaponized EMFs During the Cold War 5G Radiation Dangers – The Definitive Guide Report of final results regarding brain and heart tumors in Sprague-Dawley rats exposed from prenatal life until natural death to mobile phone radiofrequency field representative of a 1.8 GHz GSM base station environmental emission The roll out of 5G wireless service is 'a massive health experiment,' public health expert warns as cell companies install 800,000 towers across the US The Connection Between “Covid”, 5G, and the Graphene Oxide Found in the Jabs 5G is a weapons system designed to KILL people, says weapons expert Mark Steele Was 5G developed as a Directed Energy Weapon system? How the Military Deployment of 5G Weapon Systems Worldwide & Weaponized COVID-19 ‘Vaccines” were Fastidiously Integrated to Inflict Maximum Injury and Lethality 5G Will Use the Same Frequencies as Pain-Inflicting Military Weapon

Redpill Drifter

122,806 görüntüleme • 2 yıl önce

Detoxing to increase life expectancy and liver health:How legit medical practitioners are being comical (and very wrong) about health information. I like Dr. Pal Manickam. He is a Gastroenterologist from California. He makes really comical videos. Some of them make me laugh out loud. But I wish he would be more serious about the content inside his videos because a lot of it are heavy on the misinformation side. I chose to discuss this video because 1) it has garnered millions of views on Instagram and liked by more than 10K people and 2) it talks about detoxing and the liver and 3) it is standard clinician's creed/code to correct health misinformation. In the video, Dr. Pal speaks about endotoxins and exotoxins. Endotoxins he says are toxins within our body like urea and feces and exotoxins are packaged foods. I am deeply worried about his inaccuracies despite being a board certified Gastroenterologist in the USA. Endotoxins are the main component of the outer membrane of the cell wall of a specific type of bacteria - called the Gram-negative group of bacteria or GNB. GNB's are so called because do not retain the crystal violet stain used in the Gram staining method (invested by Danish microbiologist Hans Christian Gram). GNB's are characterized by their cell envelopes, which are composed of a thin peptidoglycan (made of sugars+amino acids) cell wall sandwiched between an inner cell membrane and a bacterial outer membrane. Endotoxins are literally "poisons." Their production in the body leads to inflammatory responses at the cell, tissue, organ and systems level which is taken care (neutralized) of by a series of complex process that start in the gut and involving the liver in healthy persons. Example of endotoxin is lipopolysaccharide. Urea is not an endotoxin. It is a substance formed by the breakdown of protein in the liver. The kidneys filter urea out of the blood and into the urine. Urea is the major constituent of the urine and the principal means for disposal of nitrogen derived from amino acid metabolism. Feces are not endotoxins, even though they contain endotoxins. In simple terms, feces, or excrement, is the waste matter remaining after food has been digested, absorbed and thereafter discharged from the bowels. Exotoxins are also toxins secreted by bacteria. An exotoxin can cause damage to the host by destroying cells or disrupting normal cellular metabolism. They are highly potent and can cause major damage to the host. Exotoxins may be secreted, or, similar to endotoxins, may be released when bacteria dies. Example of exotoxin is Botulinum toxin secreted by bacteria Clostridium botulinum. This toxin is notorious for causing a paralytic disease called botulism in infants when they are fed honey at birth. Packaged foods are not exotoxins. They are sources of carbohydrates, proteins and fats and have nutritive value. Toxins do not have nutritive value. In the video, Dr. Pal says our liver will clear all the toxins. He also speaks about sunrise to sunset method - eating from 7AM to 7PM and fasting from 7PM to 7AM which will help detox the body and there is no requirement for "fancy detox diets." He then advises a 24 hour water fasting once a month to detox the body. The liver does not clean all toxins. The lungs, kidneys and skin are also important "detoxifiers" in the body. A lot of misinformation is spread by doctors who "detach organ systems" from the "whole" to sell their agenda of a special practice (like gut detox diet) or sell a supplement that will help improve organ health (such as liver detox drugs) completely ignoring the fact that the "The Whole (body) is Greater than the Sum of its Parts (organs)." The Sunset-Sunrise method is a type of time-restricted eating and a "fancy diet" which Dr.Pal himself is advocating against. A recent high quality study in the New England Journal of Medicine showed that time-restricted feeding DID NOT have any benefits over calorie restriction alone in the context of weight loss, body fat changes or metabolic risk factors. Water Fasting is an extreme form of "fancy dieting" and a possibly detrimental "fad diet" which has no conclusive benefits and is not recommended by any clinical societies in the world. It is only recommended by people with anecdotal experience on the same or by those who ignorantly advocate the same without understanding scientific evidence on it, like Dr.Pal himself. An 8-day water fasting only led to sense of well-being and did not affect metabolic factors. It increased uric acid, ketosis, lowered glucose and dehydrated people and can lead to lifethreatening metabolic derangements. Prolonged water-fasting increased triglycerides and insulin resistance after refeeding, the detrimental effects of which remain unknown in long term. All the current available studies on water-fasting is on minimum 5 day to almost 6 weeks of intermittent water-fast and NONE on single day a month fasting as mentioned by Dr.Pal. Again, this advise is just bluff and there is no evidence that it would led to healthier outcomes or improve disease conditons. There is NO evidence that water fasting or time-restricted diets DETOX the body. Detox is a wellness marketing fraud term which is thrown around by people, including doctors, who deeply lack scientific temper, critical thinking and rationality.

TheLiverDoc™

248,925 görüntüleme • 3 yıl önce

🚨 HIDDEN DNA CONTAMINATION IN THE PFIZER COVID-19 VACCINE A Massive, Ignored Oncogenic Threat A presentation by Kevin McKernan, a genomics expert with deep roots in the Human Genome Project This presentation was recently given to Commissioners of Phase 2 of New Zealand’s Royal Commission of Inquiry into COVID-19 Lessons Learned. “If you look through the vaccine history and the literature, you'll know that the SV40 virus contaminated the polio vaccines, and there's a large debate in the literature that's been going on for decades as to its implication in cancer. When you give SV40 viruses to cell lines and to tissues you will get cancers, there's no question about that.....in the laboratory, this virus is one of the most potent oncogenic viruses we know of. We don't have the whole virus in these vaccines, we have some of the more carcinogenic components of that virus in the vaccines however, and I'm going to touch on some of the papers that point that out. These sequences are very functional and they have consequences when they are left behind inside of a vaccine.” “The DNA sequence that's in there is known as the SV40 promoter in the enhancer region, that's one of the regions, there's also an SV40 origin of replication that we'll touch on, and there's an SV40 polyA signal. Those are the three main pieces of DNA that are in there. The SV40 enhancers are used in gene therapy plasmids, these are nuclear targeting sequences, so these transcription factors bind to that sequence and drag it, and everything connected to it, into the nucleus of the cell. So when you hear a lot of the responses to this work, they’ll say, ‘Oh, it doesn’t matter, it’s never going to get to the nucleus.’ There are two things wrong with that statement: firstly, there’s a nuclear targeting sequence that guarantees it will get to the nucleus, secondly, these lipid nanoparticles go to cells that are dividing, and when cells divide, there is no nuclear envelope protecting the DNA. They have to go through cell division, and that dissolves during that process. So when they’re talking about this not getting to the nucleus, these people are doing a smoke screen on you. They’re not being honest about the fact that cells divide, and when cells divide, there is no protection of this DNA. That’s something to watch out for when you see people saying it doesn’t get to the nucleus, that's a sign they are trying to lie to you.” “The other literature out there shows that this SV40 promoter and enhancer binds to the p53 gene. The p53 gene is the guardian of your genome, it's a tumour suppressor gene. You don’t want anything binding to that gene, otherwise you may see an impact in cancer. This is very important given the literature we have now on the spike protein itself also inhibiting the expression of the p53 gene. Now we've got two reasons to be concerned about p53: the DNA in there interferes with it to some degree, and we know the spike protein plays a role in that pathway as well, so there's an oncogenic concern here. There is also listed literature now demonstrating that this particular sequence is known as a ‘hyper mutability element,’ it will induce mutations in DNA near it, potentially leading to tumourigenic activity. So when they say there is no function to this DNA, you can point to these three papers and say, no, there’s published function of this DNA that needs to be explained. This is not something you can dismiss by saying, well, they forgot to tell us about it. No, it’s very relevant, and there’s a reason they forgot to tell you about it: they didn’t want you to know this was in there. And you'll see that this lines up with some of their future business interests.” “The kicker here is that we’re now finding these sequences not just in the vaccine, but we're finding them in people. We don’t know if it’s integrated, but it’s there. These are studies that weren’t looking for it, and the methods they used arguably suppressed the signal significantly. There's at least five peer reviewed studies that have come out looking at RNA sequencing in vaccinated and unvaccinated people. If you dig through that data on NCBI, you can take all those reads, map them against the plasmids from the vaccine manufacturers, and you can find that DNA in these patients. There's a study from Ryan et al. that looked at 75 people in Australia, and there's a great study from Chakraborty that went though that data and demonstrated that both the Ryan paper and the Odak paper have Moderna and Pfizer vaccine sequences in the patients’ blood. So this means that the blood supply is contaminated. That’s a very serious issue if the blood banks aren’t looking for it and are re-injecting this into other people. This would normally have caused an enormous halt in any other scenario, once you find components of the vaccine that were never declared and have links to oncogenic sequences, and they are now floating around the blood supply, and no one’s doing anything about it. That should be a concern to everybody in the transfusion field.” Please retweet. Simeon Brown @TanyaUnkovichMP Chris Penk

Coronavirus Plushie

16,273 görüntüleme • 1 yıl önce

🚨EPSTEIN FILES STATE THE CREATED NEANDERTHALS CLONES Clones of Neanderthals were created in underground tunnels as stated in the Epstein files released by the DOJ government in 2026. It is impossible to ignore the truth at this point. The truth is stranger than fiction and we have not heard anything stranger than this happening in real life. Per Charlie T Griffen The first studies of Neanderthal DNA focused on the genetic sequences of mitochondria, the microscopic organelles that convert food to energy within cells. In 2005, however, 454 began a collaborative project with the Max Planck Institute in Leipzig, Germany, to sequence the full genetic code of a Neanderthal woman who died in Croatia's Vindija cave 30,000 years ago. As the Neanderthal genome is painstakingly sequenced, the archaeologists and biologists who study it will be faced with an opportunity that seemed like science fiction just 10 years ago. They will be able to look at the genetic blueprint of humankind's nearest relative and understand its biology as intimately as our own. In addition to giving scientists the ability to answer questions about Neanderthals' relationship to our own species--did we interbreed, are we separate species, who was smarter--the Neanderthal genome may be useful in researching medical treatments. Newly developed techniques could make cloning Neanderthal cells or body parts a reality within a few years. The ability to use the genes of extinct hominins is going to force the field of paleoanthropology into some unfamiliar ethical territory. There are still technical obstacles, but soon it could be possible to use that long-extinct genome to safely create a healthy, living Neanderthal clone. Should it be done? At the 454 Life Sciences offices, Gerald Irzyk, Jason Affourtit, and Thomas Jarvie explain the process they use to read the chemicals that made up Neanderthal DNA and the genes that determined a large part of their biology. DNA has a shape, called a double helix, that makes it look like a twisted ladder. Each rung on the ladder is called a base-pair. The rungs are made up of a pair of chemicals called nucleotides--adenine, thymine, cytosine, and guanine, which are usually referred to by their first initials. The sequence of the nucleotides in the DNA determines what genes an organism has and how they function. Max Planck Institute initially chose 454 because it had come up with a way to read hundreds of thousands of DNA sequences at a time. Genome-sequencing technology is advancing at a rate comparable to computer processing power. Putting the fragments themselves in order can be a little tricky. "At first glance, it's just this completely random assemblage of As, Ts, Cs, and Gs," says Irzyk. "But it turns out there are patterns and motifs, and sometimes these are very specific to a group of organisms." For the Neanderthal sample, the human and chimpanzee genomes were used as references for checking the sequence. Working with ancient DNA can be much more problematic than sequencing genetic material from living species. Within hours of death, cells begin to break down in a process called apoptosis. The dying cells release enzymes that chop up DNA into tiny pieces. In a human cell, this means that the entire three-billion-base-pair genome is reduced to fragments a few hundred base-pairs long or shorter. The DNA also goes through chemical changes that alter the nucleotides as it ages--C changes into T, and G turns into A--which can cause the gene sequence to be interpreted incorrectly. In the case of the Neanderthal sample, somewhere between 90 and 99 percent of the DNA came from bacteria and other contaminants that had found their way into the bone as it sat in the ground and in storage. The contaminant DNA has to be identified and eliminated. Given the similarity between Neanderthal and modern human DNA, this can be especially difficult when the contamination comes from the people who excavated or analyzed the bone.

SANTINO

54,154 görüntüleme • 5 ay önce

BRAVO! to Dr. Mark Trozzi for being one of the few Health Freedom MDs with the guts to openly call the Covid jabs what they are: bioweapons. "This genetic bioweapon is really a biological bull in a china shop... we know 28 mechanisms by which it causes cancer alone... [and the jabs are] permanently genetically modifying and damaging the genetic code of [humanity]." This clip of Trozzi (Dr Mark Trozzi MD), a veteran E.R. physician with 25 years of experience, as well as a human rights activist, is taken from an interview with Dr. Joe Sansone (Dr. Joseph Sansone (JosephSansone.com)) posted to Rumble on December 11, 2025. ----------------Partial transcription of clip--------------- "This genetic bioweapon is really a biological bull in a china shop. I mean it does so many damage. And I mean, I've given lectures. We were together last January, I gave a lecture in Florida on the mechanisms of injury. And the reality is you can't keep up. I mean, we know 28 mechanisms by which it causes cancer alone. "But you know, and this is, I mean it was shocking from the moment we looked at the ingredients before anyone was injected. Shocking enough to like basically set down my entire life's work to try to stop it. That's not because I'm super courage. It's, that's how serious this is. But you genetically, they're genetically modifying people, claiming they're giving them a vaccine and then genetically modifying them so that they will produce a variety of poisons. Mostly the spike protein of the man-made design, SARS-CoV-2 virus, which is the most toxic part of it. "And normally, nobody's body would be producing it. And then they're producing this, this random splay of protein junk which can trigger autoimmune diseases in every direction. And so, but then what's worse is, you know, they claimed that what was in it was modified messenger RNA, modified both so that it would screw up and create all these random proteins as well as spike protein, but modified so that it would persist and nobody knew how long. "In other words, oh, so my body is going to start producing foreign proteins and identifying itself as a foreigner to be attacked by my own immune system. But for how long? Well, nobody knows because this is completely experimental, this new N1 methyl pseudouridinated version of messenger RNA. "But as you know, and as Dr. Speicher, Dr. McKernan and others have revealed through repeated analysis around the world, 30% of the genetic material in there is DNA and it includes plasmid DNA and it includes, in the case of Pfizer, completely covered up that it could even possibly be there. And the fraud they committed to the FDA and the public health agency, european agency, et cetera, that they put in these genetic sequences which were derived from the simian virus, not the virus, but some specific genetic sequences which we've known since 1990 research. "These are genetic hacking tools. When you put foreign DNA with something like a pegylated nanoparticle into a human cell or any mammal cell, and if you deliver as well these little SV40 promoter enhancer sequences... I mean, and this is pre-existing research, that will cause the DNA to be moved into the nucleus and cause it to be incorporated. "So you're permanently genetically modifying and damaging the genetic code of the humans. And we have evidence of this now, Joseph. Some of the most shocking evidence. And I think what you've pointed out is really important. This is not just an attack on the people health that are alive right now. This is attack on our possibility to produce viable offspring and have the continuation of the human race. "We now have tests on male sperm cells where the sperm cells contain in their DNA the genetic code of the spike protein. So men's sperm has been genetically modified so they will pass this toxic genetic flaw into their children if they're able to reproduce. Every sperm cell, we don't know, we don't know how many, but many. We have evidence that 30% of a woman's eggs die shortly following the injections as a result of these injections. Assault on the ovaries where they're particularly drawn to go and deposit the genetic code. "We have cancers that have now been taken out of people. And when you look at the DNA in the cells of the cancer, that DNA has been modified by these injections. So you're looking at permanent genetic modification of human beings without their consent based on a lie that they're getting a safe and effective vaccine for a disease claiming there's no treatment for which there was good treatments. And the whole thing from the virus through the bioweapon death shot were brought to you by the same people. And we're talking about people like Fauci, Gates, Tedros, Daszak, etc."

Sense Receptor

19,495 görüntüleme • 8 ay önce

"We do it again. We do it again. We do it again. Because, this can't be. The problem is..it be. No matter how skeptical you are, be as skeptical as you'd like, but there it is." ~Bengston (This is what Mick West said he doesn't find interesting and thus, he doesn't want to interview Bengston. The truth? IMO, he's scared shitless to take on Bengston as there's too much data to refute. Psi (or whatever this is) is real and this is one of the more interesting claims in the world. How could you NOT be interested in this? How about you, Michael Shermer?) "We re-injected the mice without any treatment, and the mice were immune to cancer." ~Bengston (It's the 1970s on Long Island. A skeptical Bill Bengston is working as a lifeguard at the town pool and meets a guy, Ben, who claims to be psychic. No matter what tests Bengston comes up with, Ben passes with flying colors. Then Ben starts healing people. But how to know if they were being healed with Ben's psi or something more prosaic? Did they change their diet? Supplements? Conventional medicine? Not everybody came back so it was very hard to know. So Bengston moves to the lab where Ben would try to cure mice of a cancer that has killed every mouse ever injected within 27 days max. At the last minute, Ben drops out and Bengston is forced to be the healer.) ~ Bill Bengston: "If you watch a few hundred healings, at first it's exhilarating, but after a while it's frustrating. Because you don't know what, why, where, when, any of those things that someone interested in serious inquiry might be interested in. You were just looking at people coming in, some benefit occurred. People leaving. Sometimes they didn't come back. Sometimes it took more than one treatment. Sometimes it happened pretty quick. I think I was the fastest ever (Bengston says Ben healed his back after one short treatment). But what did? "So you come in, you have x, it's a famous algebraic disease. You have x, and you leave better. Now maybe it's the multiple treatments, you know, whatever it may be. But you leave better. What did it? Was it time? Because people get better over time. Was it belief? I didn't think it was belief, because I wasn't a believer. I was an experiencer, but not a believer. Was it the food you ate, the food you stopped eating, the grapefruit you had in the morning? I can't...I don't have the head to wrap myself around clinical questions like that. I never know why something happens, because there's too many variables and such. "And so, after watching a couple hundred healings, taking part in a couple hundred healings, I decided to...I gotta go past this. And I ran into another guy who was watching this, somewhat parallel to me. A geologist, pretty well known (David Krinsley ~Joe). And we said, 'What can we do to test this? You know, the phenomenon is seriously interesting. What could we do to really test it so that if healing occurs, there's no viable counter hypothesis.' "And at the time, he was the head of the geology department at City University of New York, and he said, 'I got some favors owed me, let me see what I can find out in the biology department. I'm pretty good friends with the chairman of the biology department there.' "And so he met with the biology chair, and he said, 'Well, let me poke around in my department and see what we can do.' And he said, 'I got the perfect study. There's a mouse model of cancer that has 100% fatality. Never been an extension of life past a month after it's been injected with cancer. There's thousands of journal articles written about this mouse and this cancer. Everybody around the world knows this mouse and this cancer. If you're in oncology, you know this mouse and this cancer, and [there] has never been a cure.' "I said, 'Let's do it. Let's find out what we can do.' "And at the time, I had no idea what to expect. So I was thinking, 'Well, maybe we can extend the life towards a month. Maybe it won't be a normal curve distribution, maybe it'll be a negatively-skewed distribution. And maybe the mouse will live to the end of their lifespan and all that. "We had no idea what to expect. "So we got a cage of mice. I held the cage of mice for an hour at a time in the lab at Queens College, City University, and we watched as the tumors grew. And I was sure this was failing. And incidentally, I'm almost always wrong. I expected, if we got to the mice right after injection and we treated them a couple times, enough, every day - we didn't know - if we treated them every day, they wouldn't develop cancer. I was thinking, you know, it's something like radiation. You know, you go, 'Zzt, zzt,' and you zap the mice and the tumors, or the cancer cells die, or something along those lines. I was thinking conventional oncology. "And so, I put my hands around the cage of mice, treated them every day, the tumors started to grow anyway, and I wanted to call off the experiment. You know, it shows you how much I believe. I got talked into going a couple extra days, and the tumors developed these blackened areas. And I said, 'Let's call it off, didn't work. You know, we tried it. Didn't work.' "Go a couple more days. Tumors started to ulcerate, and so there was this raw part of a tumor. And I said, 'Would you pay attention? It doesn't work!' Couple more days. And then the tumors suddenly imploded, and the mice were cured. They weren't remitted, they were cured. And by that, I mean it wasn't a suppression of symptoms, it wasn't a temporary reduction in symptoms. It was...there was no cancer in the mouse at all. "And it's farther than that. We re-injected the mice without any treatment, and the mice were immune to cancer. Now that's reasonably interesting. "So, first thing you do is, I, as a skeptic, go, 'Umm, this doesn't make any sense (laughs). Let's do it again. But let's not do it with just me, let's do it with some volunteers.' "So I had a couple of faculty volunteers who thought this thing was insane, and they were right. So I had a couple of faculty volunteers, they got a couple of student volunteers. All non-believers, no experience in any of this hocus pocus. Taught 'em the little technique that I had developed. They treated the mice, the exact same pattern: Tumor grows, blackened area, ulceration, implosion, full lifespan cure. "We do it again. We do it again. We do it again. Because, this can't be. The problem is..it be." (Both laugh) "It's just, you know, no matter how skeptical you are, be as skeptical as you'd like, but there it is. You know, I deny this gravity, you know? I don't believe in gravity. There is gravity. I don't believe in this healing. There is healing. "I just finished, recently, my twentieth mouse experiment, I'm a little slow. I've done it in, I think, six medical schools, equal number of other biology labs. And I just finished at Tokyo University, multiple strains of cancer and details you don't care about. "And so, I have done, at this point, twenty mouse experiments, multiple medical schools, many cell experiments. I've done many experiments. That's the really short version. A hundred years truncated into a couple of paragraphs."

Joe Murgia

12,705 görüntüleme • 1 yıl önce