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Abdominal CT Tutorials - Pyelonephritis versus renal infarct (1/2) Classic uncomplicated pyelonephritis Coronal + liver windows are very helpful Radiopaedia.org case link:

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Michael Hartung

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19,028 görüntüleme • 1 yıl önce •via X (Twitter)

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(2/2) Renal infarction @Radiopaedia Case link:

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For more video lessons with scrollable cases, quizzes, and review sets, check out my course: #FOAMed #MedEd #FOAMRad #RadEd #RadRes #radiology #EmergencyMedicine

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Abdominal CT Tutorials - Mesenteric ischemia (1/2) SMA embolus it's often hard to see what's not there... Case link:
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PSA: General-purpose multimodal models, like Gemini 2.0, Grok-2, and GPT-4o are NOT good at interpreting medical images. This is expected, as they were not trained for this purpose. Last week, I shared a video of Gemini 2.0 Realtime looking at a CT that went viral. It was an extremely simple case (Case 1 in my call prep course on Navigating Radiology), and I asked very simple questions. Given the context - screensharing with a general model - I was genuinely impressed that it could identify some very basic anatomy and an abnormal pancreas in realtime! The video demonstrated the power of interacting with AI this way, and the potential for future medical-specific models to be used similarly. BUT many reposts of the video perpetuated misconceptions: AI replacing radiologists, Grok can read your scans, etc. Naturally, this video will likely not go viral, but here’s an example of what frequently happens with general-purpose models: many basic errors (calling the prostate the bladder, and the bladder the uterus), seeing masses that don't exist, etc - often probabilistic based on context. That said, interacting with LLMs real time with screensharing IS a very cool unlock, with a lot of potential. Very exciting!
1:35

PSA: General-purpose multimodal models, like Gemini 2.0, Grok-2, and GPT-4o are NOT good at interpreting medical images. This is expected, as they were not trained for this purpose. Last week, I shared a video of Gemini 2.0 Realtime looking at a CT that went viral. It was an extremely simple case (Case 1 in my call prep course on Navigating Radiology), and I asked very simple questions. Given the context - screensharing with a general model - I was genuinely impressed that it could identify some very basic anatomy and an abnormal pancreas in realtime! The video demonstrated the power of interacting with AI this way, and the potential for future medical-specific models to be used similarly. BUT many reposts of the video perpetuated misconceptions: AI replacing radiologists, Grok can read your scans, etc. Naturally, this video will likely not go viral, but here’s an example of what frequently happens with general-purpose models: many basic errors (calling the prostate the bladder, and the bladder the uterus), seeing masses that don't exist, etc - often probabilistic based on context. That said, interacting with LLMs real time with screensharing IS a very cool unlock, with a lot of potential. Very exciting!

Rajesh Bhayana

21,576 görüntüleme • 1 yıl önce

How to determine exactly which local business to start in less than 4 minutes. No exaggeration, watch the video! If you're into text, these are the 4 steps: 1 Pick 4-6 industries. In this case, landscaping, roofing, plumbing & electrical 2 Pick a city to run a scrape 3 Run the scrape with exact match categories only 4 Open an excel pivot table to see how the # of local businesses compare against the national average Everything is shown in the video, step by step. Run the scrape with this tool: (yes, that's an affiliate link. I'll make a whopping $1-3 if you use it and you'll save 20%. sue me!) Use this link to see the list of google maps categories, sorted by the ones that appear most to least often: - Insanely helpful. If this doesn't make sense then the short video below will. This tweet only took ~15 mins to write but 15 years to learn. You can say thanks with a follow, comment or share Chris Koerner
3:55

How to determine exactly which local business to start in less than 4 minutes. No exaggeration, watch the video! If you're into text, these are the 4 steps: 1 Pick 4-6 industries. In this case, landscaping, roofing, plumbing & electrical 2 Pick a city to run a scrape 3 Run the scrape with exact match categories only 4 Open an excel pivot table to see how the # of local businesses compare against the national average Everything is shown in the video, step by step. Run the scrape with this tool: (yes, that's an affiliate link. I'll make a whopping $1-3 if you use it and you'll save 20%. sue me!) Use this link to see the list of google maps categories, sorted by the ones that appear most to least often: - Insanely helpful. If this doesn't make sense then the short video below will. This tweet only took ~15 mins to write but 15 years to learn. You can say thanks with a follow, comment or share Chris Koerner

Chris Koerner

133,275 görüntüleme • 2 yıl önce

🚨Dr. William Makis: Ivermectin Dosing for Cancer Explained In one of his recent talks, Dr. William Makis shared what he considers the most important dosing guide for using Ivermectin in cancer. According to Dr. Makis, the starting dose for most cancers is 1 mg per kilogram of body weight per day For example, a person weighing 60 kg would take 60 mg daily, that’s five 12 mg pills or roughly one teaspoon (6 ml) of liquid ivermectin. He mentioned that Ivermectin has shown positive effects in many types of cancer, including: - Breast cancer - Colon cancer - Lung cancer - Pancreatic cancer - Gastric cancer - Renal cell carcinoma - Leukemias He noted that there is very little research on lymphomas, but that doesn’t mean it won’t work, it simply hasn’t been studied much yet. Important points from Dr. Makis: 1) The anti-cancer effect of Ivermectin appears to be dose dependent. 2) Higher doses may offer better results in more aggressive cancers. 3) For very aggressive cancers (such as pancreatic, leukemia, or brain cancers), he suggests considering 2 mg/kg or even up to 2.5 mg/kg per day. Some patients have used these higher doses for many months with only temporary side effects (such as mild visual disturbances that usually resolve within a few days). Real-world examples include a prostate cancer patient whose PSA dropped from 89 to 11 on 45 mg daily, and a terminal gallbladder cancer case that resolved after 14 months on 2 mg/kg. Dr. Makis emphasizes that Ivermectin is a very safe drug with no reported long-term side effects at 1 mg/kg. He recommends starting at this dose and adjusting upwards depending on the individual case and cancer type. He also stresses that people can safely stay on Ivermectin for months as long as there is active disease. If you're researching Ivermectin for cancer protocols, many people are choosing GENIX MEDS for clean, pharmaceutical-grade Ivermectin with straightforward worldwide delivery. #Ivermectindosage #MakisMD #Genixmeds
5:47

🚨Dr. William Makis: Ivermectin Dosing for Cancer Explained In one of his recent talks, Dr. William Makis shared what he considers the most important dosing guide for using Ivermectin in cancer. According to Dr. Makis, the starting dose for most cancers is 1 mg per kilogram of body weight per day For example, a person weighing 60 kg would take 60 mg daily, that’s five 12 mg pills or roughly one teaspoon (6 ml) of liquid ivermectin. He mentioned that Ivermectin has shown positive effects in many types of cancer, including: - Breast cancer - Colon cancer - Lung cancer - Pancreatic cancer - Gastric cancer - Renal cell carcinoma - Leukemias He noted that there is very little research on lymphomas, but that doesn’t mean it won’t work, it simply hasn’t been studied much yet. Important points from Dr. Makis: 1) The anti-cancer effect of Ivermectin appears to be dose dependent. 2) Higher doses may offer better results in more aggressive cancers. 3) For very aggressive cancers (such as pancreatic, leukemia, or brain cancers), he suggests considering 2 mg/kg or even up to 2.5 mg/kg per day. Some patients have used these higher doses for many months with only temporary side effects (such as mild visual disturbances that usually resolve within a few days). Real-world examples include a prostate cancer patient whose PSA dropped from 89 to 11 on 45 mg daily, and a terminal gallbladder cancer case that resolved after 14 months on 2 mg/kg. Dr. Makis emphasizes that Ivermectin is a very safe drug with no reported long-term side effects at 1 mg/kg. He recommends starting at this dose and adjusting upwards depending on the individual case and cancer type. He also stresses that people can safely stay on Ivermectin for months as long as there is active disease. If you're researching Ivermectin for cancer protocols, many people are choosing GENIX MEDS for clean, pharmaceutical-grade Ivermectin with straightforward worldwide delivery. #Ivermectindosage #MakisMD #Genixmeds

GENIX MEDS

19,878 görüntüleme • 1 ay önce

Dangers of coffee? Once again, the Sattvic Movement has outdone itself with this utter nonsense of a video that misleads public on coffee. The Sattvic Movement is a pseudo-intellectual, pseudo-scientific, spinal-level thinking nationalistic activism from a scientifically illiterate couple, that is leveraged on peddling anti-science concepts, demonizing scientific progression, misinterpreting evidence, and misrepresenting clinical data all the while promoting ancient and primitive superstition written in the religious texts of Ayurveda which promotes culture-traditional dogmatism in healthcare. Even a grade 4 glioblastoma is not as malignant as Sattvic Movement is to India’s scientific temper. In this video, Lady Sattvic speaks about three “facts” on why coffee is dangerous. 1/ Coffee is just for energizing temporarily and then people who drink coffee become lethargic. 2/ People get physically and psychologically dependent on coffee. 3/ Coffee dehydrates and destroys the lining of the stomach and causes constipation. Her solution: Have warm herbal teas! These statements are proof that mental constipation leads to verbal diarrhea and none of these are true. Coffee does not produce a jerk and flaccid response in the nervous system, but caffeine may. In fact, coffee as a dietary supplement for health/disease is one of the most scientifically studied aspects in clinical medicine. Three cups of black coffee without milk or sugar daily have immense health benefits that you need to know about! The Sattvic Movement is just peddling a whole bunch of lies. Coffee is significantly beneficial for the liver: it reduces fatty liver disease, reduced progression of fatty liver disease, reduces risk of developing cirrhosis and reduces risk of liver cancer development. See here here and here Coffee consumption does not only reduce risk of liver cancer, but also breast and endometrial cancer in women, colorectal and prostate cancers in men, reduces risk of dying from all causes, especially metabolic diseases such as diabetes and heart diseases and reduces risk of developing diabetes type 2 and Parkinson’s disease. See here here here People do not get dependent on coffee, but caffeine. Do you know what else contains caffeine apart from coffee? Tea and chocolates. Yes. Dark chocolate contains 43g of caffeine in 100g, coffee contains 20-40g depending on preparatory methods and tea contains 11g caffeine in 100g. So, is shifting to tea the solution to prevent caffeine dependency? Nope. Avoiding caffeinated products is. What does that mean? It means that decaffeinated coffee is as good as whole coffee, because the “goodness and benefits on health” of coffee is not dependent on caffeine, but polyenol compounds in coffee. See here and here And guess what, coffee and caffeine consumption was also significantly associated with decreased risk of depression. Yes, see here: and hey also this – coffee intake was associated with lower incidence of chronic kidney disease, end-stage kidney disease and protein loss in urine. Damn. Coffee is the superhero we all need! See here - So go ahead and enjoy some raw and real/or decaff that will increase longevity, reduce heart and metabolic diseases, cancers and reduce risk of developing degenerative brain diseases. Ok, so what about herbal teas? It is a bummer. There is absolutely no evidence from clinical studies to showcase that herbal teas are useful for anything other than featuring in misleading, stupid Instagram reels. But wait, there is more on herbal teas. Herbal teas are not all that safe. Herbal teas, especially green tea extract infusions were associated with liver injury, liver failure and death or organ transplantation. The European Union warned and limited the use of green tea extracts in foods fearing liver damage among consumers. See here and here And if you look at benefits of herbal teas versus adverse events of herbal teas in published literature, you will see that adverse events feature more. Herbal teas have caused liver injury, liver failure, multiple organ failure, accelerated hypertension, paralysis, chronic liver injury, heart failure, brain strokes and brain failure and so much more in humans! See this link: Oh, by the way, coffee does not increase blood pressure. In fact, it lowers it. So do not be too miserable on that. In habitual coffee users (3-5 cups a day), coffee had benefits on blood pressure parameters. Do not believe me? See here: and about that destroying stomach lining and causing constipation – that was just bluff from the annoyingly sounding Lady Sattvic. See here But is coffee safe for all? No. Pregnant women, please avoid more than 1-2 cups a day. See here: So, what is this Sattvic Movement all about? It is all about destroying the scientific temperament of the public in India and by misleading the public, they are creating more patients for the modern medicine hospitals to treat. Are they funded by Big Pharma? Hmmm, I wonder. I am going to think that over a hot cup of black coffee. I think you should too! And don’t forget to share this information with your herbal tea lover friends!
1:11

Dangers of coffee? Once again, the Sattvic Movement has outdone itself with this utter nonsense of a video that misleads public on coffee. The Sattvic Movement is a pseudo-intellectual, pseudo-scientific, spinal-level thinking nationalistic activism from a scientifically illiterate couple, that is leveraged on peddling anti-science concepts, demonizing scientific progression, misinterpreting evidence, and misrepresenting clinical data all the while promoting ancient and primitive superstition written in the religious texts of Ayurveda which promotes culture-traditional dogmatism in healthcare. Even a grade 4 glioblastoma is not as malignant as Sattvic Movement is to India’s scientific temper. In this video, Lady Sattvic speaks about three “facts” on why coffee is dangerous. 1/ Coffee is just for energizing temporarily and then people who drink coffee become lethargic. 2/ People get physically and psychologically dependent on coffee. 3/ Coffee dehydrates and destroys the lining of the stomach and causes constipation. Her solution: Have warm herbal teas! These statements are proof that mental constipation leads to verbal diarrhea and none of these are true. Coffee does not produce a jerk and flaccid response in the nervous system, but caffeine may. In fact, coffee as a dietary supplement for health/disease is one of the most scientifically studied aspects in clinical medicine. Three cups of black coffee without milk or sugar daily have immense health benefits that you need to know about! The Sattvic Movement is just peddling a whole bunch of lies. Coffee is significantly beneficial for the liver: it reduces fatty liver disease, reduced progression of fatty liver disease, reduces risk of developing cirrhosis and reduces risk of liver cancer development. See here here and here Coffee consumption does not only reduce risk of liver cancer, but also breast and endometrial cancer in women, colorectal and prostate cancers in men, reduces risk of dying from all causes, especially metabolic diseases such as diabetes and heart diseases and reduces risk of developing diabetes type 2 and Parkinson’s disease. See here here here People do not get dependent on coffee, but caffeine. Do you know what else contains caffeine apart from coffee? Tea and chocolates. Yes. Dark chocolate contains 43g of caffeine in 100g, coffee contains 20-40g depending on preparatory methods and tea contains 11g caffeine in 100g. So, is shifting to tea the solution to prevent caffeine dependency? Nope. Avoiding caffeinated products is. What does that mean? It means that decaffeinated coffee is as good as whole coffee, because the “goodness and benefits on health” of coffee is not dependent on caffeine, but polyenol compounds in coffee. See here and here And guess what, coffee and caffeine consumption was also significantly associated with decreased risk of depression. Yes, see here: and hey also this – coffee intake was associated with lower incidence of chronic kidney disease, end-stage kidney disease and protein loss in urine. Damn. Coffee is the superhero we all need! See here - So go ahead and enjoy some raw and real/or decaff that will increase longevity, reduce heart and metabolic diseases, cancers and reduce risk of developing degenerative brain diseases. Ok, so what about herbal teas? It is a bummer. There is absolutely no evidence from clinical studies to showcase that herbal teas are useful for anything other than featuring in misleading, stupid Instagram reels. But wait, there is more on herbal teas. Herbal teas are not all that safe. Herbal teas, especially green tea extract infusions were associated with liver injury, liver failure and death or organ transplantation. The European Union warned and limited the use of green tea extracts in foods fearing liver damage among consumers. See here and here And if you look at benefits of herbal teas versus adverse events of herbal teas in published literature, you will see that adverse events feature more. Herbal teas have caused liver injury, liver failure, multiple organ failure, accelerated hypertension, paralysis, chronic liver injury, heart failure, brain strokes and brain failure and so much more in humans! See this link: Oh, by the way, coffee does not increase blood pressure. In fact, it lowers it. So do not be too miserable on that. In habitual coffee users (3-5 cups a day), coffee had benefits on blood pressure parameters. Do not believe me? See here: and about that destroying stomach lining and causing constipation – that was just bluff from the annoyingly sounding Lady Sattvic. See here But is coffee safe for all? No. Pregnant women, please avoid more than 1-2 cups a day. See here: So, what is this Sattvic Movement all about? It is all about destroying the scientific temperament of the public in India and by misleading the public, they are creating more patients for the modern medicine hospitals to treat. Are they funded by Big Pharma? Hmmm, I wonder. I am going to think that over a hot cup of black coffee. I think you should too! And don’t forget to share this information with your herbal tea lover friends!

TheLiverDoc™

359,386 görüntüleme • 3 yıl önce

"[C19-jab] myocarditis is real... people are going to die 20–30 years earlier than they... would have... [but the] strokes are worse... [and]...renal failure—it's 150 times more [deaths]... they selected myocarditis... to plant in the mind of the viewer that it's extremely rare" This clip of electrical engineer and independent investigator John Beaudoin, Sr. (John Beaudoin, Sr., The Real CdC, The Last Boomer) is taken from an interview with Dr. Sherri Tenpenny (Dr Sherri Tenpenny) that was posted to Rumble on June 2, 2025. ----------------Partial transcription of clip--------------- "Myocarditis is real and it affects a lot of people. It goes unnoticed. And I, I do believe it's a very big problem. In fact, I stated two, three years ago that, people are going to die 20, 30 years earlier than they otherwise would have, but they're not going to know it for 30 or 40 years and it's not going to be attributed to the vaccine. If you scar something, it's less elastic, it's not going to last as long, and myocytes don't grow back and you know more than I do. "So there's that aspect. The other is if somebody's a 4 minute, 30 second miler, they run the mile in 4:30. Right. They may never be able to run that mile better than 4:50. They've decreased the performance, but only an elite athlete in the world is going to know they've decreased the performance of their heart. If you take a regular person, the only way they're going to notice it is if, if they come into a situation where they need peak performance and then they kind of just drop dead, because they can't hit that performance anymore. Whether it's lifting a car off a person or, you know, just getting excited about something, they're just not athletes. So they, they might just drop dead. "So myocarditis. Yeah, it's 1% of the deaths though, because a lot of deaths haven't happened yet. The reason why I'm so bent on the myocarditis is because deaths involving acute renal failure. If you look at excess myocarditis versus excess acute renal failure, it's 150 times more than myocarditis. 150 times. And goes down into the teenage years. So it, yeah, 150 times. That's. How many people, a quarter of a million people and excess more than normal died from acute renal failure in the United States in the last four years. I don't know why people aren't talking about it. I don't get it. "I mean, strokes are worse than myocarditis. Pulmonary emboli far worse than myocarditis. Like, 30 times. Right. When you go down the even, even cancers, I, I can't remember the numbers. Trying to do the math in my head right now. I don't know. Eight times. I think it's, I think it's around eight times more. Oh, that's lymph node cancer. Sorry, that's specifically lymph node cancer. Yeah, it's, it's a lot everything is more than myocarditis. "I believe that they selected myocarditis. They being whoever's in charge of social media, promotion and suppression. They allowed those who were talking about myocarditis to have the platform to have the ear of the people. Because hardly anybody knows anybody who died of myocarditis. We see some in the, in the news, but you don't know anybody down the street. And when somebody down the street gets kidney failure and you don't attribute it to the vaccine, nobody's told them that, yes, kidney failure is caused by the vaccine in addition to the hospital homicides and protocols that occur with remdesivir and so forth. "But I've had people tell me even now, in 2025, even within the past couple of weeks, 'Oh, thank you for telling me that the vaccine causes acute renal failure. I didn't know.' I've been saying it for three years. I can't get the word out there. And the doctors are all talking about myocarditis. And what that does is it plants in the mind of the viewer that it's extremely rare."
3:23

"[C19-jab] myocarditis is real... people are going to die 20–30 years earlier than they... would have... [but the] strokes are worse... [and]...renal failure—it's 150 times more [deaths]... they selected myocarditis... to plant in the mind of the viewer that it's extremely rare" This clip of electrical engineer and independent investigator John Beaudoin, Sr. (John Beaudoin, Sr., The Real CdC, The Last Boomer) is taken from an interview with Dr. Sherri Tenpenny (Dr Sherri Tenpenny) that was posted to Rumble on June 2, 2025. ----------------Partial transcription of clip--------------- "Myocarditis is real and it affects a lot of people. It goes unnoticed. And I, I do believe it's a very big problem. In fact, I stated two, three years ago that, people are going to die 20, 30 years earlier than they otherwise would have, but they're not going to know it for 30 or 40 years and it's not going to be attributed to the vaccine. If you scar something, it's less elastic, it's not going to last as long, and myocytes don't grow back and you know more than I do. "So there's that aspect. The other is if somebody's a 4 minute, 30 second miler, they run the mile in 4:30. Right. They may never be able to run that mile better than 4:50. They've decreased the performance, but only an elite athlete in the world is going to know they've decreased the performance of their heart. If you take a regular person, the only way they're going to notice it is if, if they come into a situation where they need peak performance and then they kind of just drop dead, because they can't hit that performance anymore. Whether it's lifting a car off a person or, you know, just getting excited about something, they're just not athletes. So they, they might just drop dead. "So myocarditis. Yeah, it's 1% of the deaths though, because a lot of deaths haven't happened yet. The reason why I'm so bent on the myocarditis is because deaths involving acute renal failure. If you look at excess myocarditis versus excess acute renal failure, it's 150 times more than myocarditis. 150 times. And goes down into the teenage years. So it, yeah, 150 times. That's. How many people, a quarter of a million people and excess more than normal died from acute renal failure in the United States in the last four years. I don't know why people aren't talking about it. I don't get it. "I mean, strokes are worse than myocarditis. Pulmonary emboli far worse than myocarditis. Like, 30 times. Right. When you go down the even, even cancers, I, I can't remember the numbers. Trying to do the math in my head right now. I don't know. Eight times. I think it's, I think it's around eight times more. Oh, that's lymph node cancer. Sorry, that's specifically lymph node cancer. Yeah, it's, it's a lot everything is more than myocarditis. "I believe that they selected myocarditis. They being whoever's in charge of social media, promotion and suppression. They allowed those who were talking about myocarditis to have the platform to have the ear of the people. Because hardly anybody knows anybody who died of myocarditis. We see some in the, in the news, but you don't know anybody down the street. And when somebody down the street gets kidney failure and you don't attribute it to the vaccine, nobody's told them that, yes, kidney failure is caused by the vaccine in addition to the hospital homicides and protocols that occur with remdesivir and so forth. "But I've had people tell me even now, in 2025, even within the past couple of weeks, 'Oh, thank you for telling me that the vaccine causes acute renal failure. I didn't know.' I've been saying it for three years. I can't get the word out there. And the doctors are all talking about myocarditis. And what that does is it plants in the mind of the viewer that it's extremely rare."

Sense Receptor

27,511 görüntüleme • 1 yıl önce

Toxic Playgrounds...Cancer Increases 10 Times When Grass Is Replaced With 'Rubber Tire Crumb.' "Rubber Manufacturers Call It A Success With Huge Profits, While Children Are Diagnosed With Lymphoma & Leukemia." Layne Kilpatrick Shredded Tires Contain 90+ Toxins & Heavy Metals. Rubber tires are filled with carcinogens, neurotoxins & endocrine disruptors. These are the compounds we know for sure, there are unknown compounds because manufacturers are not required by law to reveal all of the chemicals used. Rubber tire crumb contains 100s of harmful chemicals like lead, mercury, arsenic & other heavy metals, benzene, PFAS, Volatile Organic Compounds (VOCs) & phthalates. These toxins don’t break down, they are causative for cancer (especially lymphoma & leukemia) , liver problems, thyroid issues, birth defects, kidney disease, decreased immunity & other chronic health conditions. Rubber manufacturers association considers it an absolute success story as it saves them money from disposing of the tires at landfills that they previously had to pay for & repurposed tires provides trillions of dollars in profits when cities purchase playground & sports field contracts using their rubber tire crumb. Millions of discarded tires, which are processed into shreds & tire crumb granules, previously were a huge cost in the billions, as landfills charged a fee for each & every tire discarded. This trillion dollar industry is always profits over people...& our children are paying the price. Real grass playgrounds & sports fields are safe for humans, wildlife & the environment. Natural grass has the benefit of oxygenating the air, capturing carbon & absorbing water, which reduces flooding & stormwater runoff. If you can’t avoid playgrounds & sport fields with rubber tire crumb, there are ways for reducing exposure to toxins & cancer causing chemicals: #1: Always wear shoes on rubber tire crumb & have good ventilation if you're playing on an indoor field by opening doors/windows & using fans. #2: Avoid using it for passive activities like sitting, lounging or picnicking & shake out any sports equipment bags to avoid transporting rubber tire crumb in vehicles. #3: Monitor young children to prevent ingestion of rubber & clean any cuts & abrasions with soap & water. #4: Avoid playing on rubber turf on very hot days & wash hands before eating, drinking, or adjusting mouth guards. #5: At home, take off shoes before entering to avoid tracking in rubber tire crumb, try to brush hair right away & shower as soon as possible. 👇92 Toxins Found In Rubber Tire Crumb👇 👇Artificial Turf & Rubber Tire Toxicity👇 👇The Hidden Truth Behind Rubber Playgrounds👇 Speaker: @hormonespecialist Layne Kilpatrick
1:17

Toxic Playgrounds...Cancer Increases 10 Times When Grass Is Replaced With 'Rubber Tire Crumb.' "Rubber Manufacturers Call It A Success With Huge Profits, While Children Are Diagnosed With Lymphoma & Leukemia." Layne Kilpatrick Shredded Tires Contain 90+ Toxins & Heavy Metals. Rubber tires are filled with carcinogens, neurotoxins & endocrine disruptors. These are the compounds we know for sure, there are unknown compounds because manufacturers are not required by law to reveal all of the chemicals used. Rubber tire crumb contains 100s of harmful chemicals like lead, mercury, arsenic & other heavy metals, benzene, PFAS, Volatile Organic Compounds (VOCs) & phthalates. These toxins don’t break down, they are causative for cancer (especially lymphoma & leukemia) , liver problems, thyroid issues, birth defects, kidney disease, decreased immunity & other chronic health conditions. Rubber manufacturers association considers it an absolute success story as it saves them money from disposing of the tires at landfills that they previously had to pay for & repurposed tires provides trillions of dollars in profits when cities purchase playground & sports field contracts using their rubber tire crumb. Millions of discarded tires, which are processed into shreds & tire crumb granules, previously were a huge cost in the billions, as landfills charged a fee for each & every tire discarded. This trillion dollar industry is always profits over people...& our children are paying the price. Real grass playgrounds & sports fields are safe for humans, wildlife & the environment. Natural grass has the benefit of oxygenating the air, capturing carbon & absorbing water, which reduces flooding & stormwater runoff. If you can’t avoid playgrounds & sport fields with rubber tire crumb, there are ways for reducing exposure to toxins & cancer causing chemicals: #1: Always wear shoes on rubber tire crumb & have good ventilation if you're playing on an indoor field by opening doors/windows & using fans. #2: Avoid using it for passive activities like sitting, lounging or picnicking & shake out any sports equipment bags to avoid transporting rubber tire crumb in vehicles. #3: Monitor young children to prevent ingestion of rubber & clean any cuts & abrasions with soap & water. #4: Avoid playing on rubber turf on very hot days & wash hands before eating, drinking, or adjusting mouth guards. #5: At home, take off shoes before entering to avoid tracking in rubber tire crumb, try to brush hair right away & shower as soon as possible. 👇92 Toxins Found In Rubber Tire Crumb👇 👇Artificial Turf & Rubber Tire Toxicity👇 👇The Hidden Truth Behind Rubber Playgrounds👇 Speaker: @hormonespecialist Layne Kilpatrick

Valerie Anne Smith

154,571 görüntüleme • 11 ay önce

🚨EXPOSED: Why Is Paxlovid – Pushed for Mild COVID – Loaded with an HIV/AIDS Drug & a BLACK BOX WARNING for Deadly Interactions? Imagine popping a pill for a sniffle, only to risk heart arrhythmias, liver failure, or worse - because it supercharges your other meds like a rogue engine. That's Paxlovid (nirmatrelvir/ritonavir) in a nutshell. The ritonavir? It's an HIV/AIDS drug, included as a 'booster' to turn your body into a drug interaction minefield. The FDA slaps a **BLACK BOX WARNING** on it, the strongest harm causing warning just shy of it being pulled from the market: "Significant drug interactions...may lead to greater exposure of certain concomitant medications, resulting in potentially severe, life-threatening, or fatal events." Contraindicated with over 100 common drugs – from statins to blood thinners – risking everything from myopathy to bleeding crises. For mild cases of COVID or influenza? The risk-reward math doesn't add up. This drug is not worth the harms. **Key Harms & Adverse Events – Don't Ignore These Red Flags:** • Virologic Rebound (COVID Returns Worse): 20% of patients (1 in 5) get rebound COVID, prolonging illness & spread. A Mass General Brigham study tracked this in real-world use, urging caution for low-risk folks. • Neurological Nightmares: Paxlovid triggers 3X more neurological adverse events than other drugs combined – think headaches, dizziness, neuropathy, even seizures in vulnerable patients. A 2025 analysis of 11,792 reports flagged this as a "strong signal." • Liver & Pancreas Damage: Hepatotoxicity is real -clinical hepatitis, jaundice reported with ritonavir. One Stanford trial noted serious hepatitis. • Kidney Strain & Failure Risk: Severe renal impairment with worsened outcomes. A 2025 cohort showed higher short- & long-term adverse events like acute injury. • Cardiac Chaos from Interactions: Ritonavir boosts antiarrhythmics like amiodarone, risking deadly QT prolongation & torsades. Contraindicated combos spike hypertension & heart events; UK MHRA alerts on this. • Severe Allergic & Skin Reactions: Anaphylaxis, Stevens-Johnson Syndrome (SJS), Toxic Epidermal Necrolysis (TEN) – blistering skin peeling off in sheets. FDA logs these cases in post marketing, even after one dose; discontinue ASAP. • Gut & Sensory Torment: Dysgeusia (metallic taste, 5-6% incidence), diarrhea (3%), nausea, vomiting hit hard, tanking adherence. Nature's 2024 meta-analysis also flags elevated D-dimer (clot risk) & ALT (liver marker). • Drug-Related Problems (DRPs) Galore: A 2024 PubMed study found high frequency of severe DRPs – interactions causing toxicity or inefficacy – in 30%+ of scrips. • HIV Resistance Roulette: If undiagnosed HIV lurks, ritonavir could breed resistant strains, dooming future treatments. This isn't fearmongering – it's FDA facts & peer-reviewed red flags from 2024-2025 studies. Early treatment like any case of influenza, involves supporting the body, detox pathways & immune response. Whole food vitamin C from acerola cherry or berries, sun exposure, rest, antioxidants such as onion, garlic, bromelain & monitoring suffices without the adverse event toxic gamble. Your health isn't worth the black box bet. What did you implement to heal from COVID or other influenza symptoms? There are very highly effective natural cures & big pharma toxic antivirals are b=never needed. My husband & I used Dr Zelenko (may he RIP) protocol as both prevention & treatment. And then implemented high dose Zinc Picolinate to heal acute zinc deficiency which is the cause of losing taste/smell with all viral illnesses including COVID. Taste/smell returned in 72 hrs. Cited research linked below in replies...
4:11

🚨EXPOSED: Why Is Paxlovid – Pushed for Mild COVID – Loaded with an HIV/AIDS Drug & a BLACK BOX WARNING for Deadly Interactions? Imagine popping a pill for a sniffle, only to risk heart arrhythmias, liver failure, or worse - because it supercharges your other meds like a rogue engine. That's Paxlovid (nirmatrelvir/ritonavir) in a nutshell. The ritonavir? It's an HIV/AIDS drug, included as a 'booster' to turn your body into a drug interaction minefield. The FDA slaps a **BLACK BOX WARNING** on it, the strongest harm causing warning just shy of it being pulled from the market: "Significant drug interactions...may lead to greater exposure of certain concomitant medications, resulting in potentially severe, life-threatening, or fatal events." Contraindicated with over 100 common drugs – from statins to blood thinners – risking everything from myopathy to bleeding crises. For mild cases of COVID or influenza? The risk-reward math doesn't add up. This drug is not worth the harms. **Key Harms & Adverse Events – Don't Ignore These Red Flags:** • Virologic Rebound (COVID Returns Worse): 20% of patients (1 in 5) get rebound COVID, prolonging illness & spread. A Mass General Brigham study tracked this in real-world use, urging caution for low-risk folks. • Neurological Nightmares: Paxlovid triggers 3X more neurological adverse events than other drugs combined – think headaches, dizziness, neuropathy, even seizures in vulnerable patients. A 2025 analysis of 11,792 reports flagged this as a "strong signal." • Liver & Pancreas Damage: Hepatotoxicity is real -clinical hepatitis, jaundice reported with ritonavir. One Stanford trial noted serious hepatitis. • Kidney Strain & Failure Risk: Severe renal impairment with worsened outcomes. A 2025 cohort showed higher short- & long-term adverse events like acute injury. • Cardiac Chaos from Interactions: Ritonavir boosts antiarrhythmics like amiodarone, risking deadly QT prolongation & torsades. Contraindicated combos spike hypertension & heart events; UK MHRA alerts on this. • Severe Allergic & Skin Reactions: Anaphylaxis, Stevens-Johnson Syndrome (SJS), Toxic Epidermal Necrolysis (TEN) – blistering skin peeling off in sheets. FDA logs these cases in post marketing, even after one dose; discontinue ASAP. • Gut & Sensory Torment: Dysgeusia (metallic taste, 5-6% incidence), diarrhea (3%), nausea, vomiting hit hard, tanking adherence. Nature's 2024 meta-analysis also flags elevated D-dimer (clot risk) & ALT (liver marker). • Drug-Related Problems (DRPs) Galore: A 2024 PubMed study found high frequency of severe DRPs – interactions causing toxicity or inefficacy – in 30%+ of scrips. • HIV Resistance Roulette: If undiagnosed HIV lurks, ritonavir could breed resistant strains, dooming future treatments. This isn't fearmongering – it's FDA facts & peer-reviewed red flags from 2024-2025 studies. Early treatment like any case of influenza, involves supporting the body, detox pathways & immune response. Whole food vitamin C from acerola cherry or berries, sun exposure, rest, antioxidants such as onion, garlic, bromelain & monitoring suffices without the adverse event toxic gamble. Your health isn't worth the black box bet. What did you implement to heal from COVID or other influenza symptoms? There are very highly effective natural cures & big pharma toxic antivirals are b=never needed. My husband & I used Dr Zelenko (may he RIP) protocol as both prevention & treatment. And then implemented high dose Zinc Picolinate to heal acute zinc deficiency which is the cause of losing taste/smell with all viral illnesses including COVID. Taste/smell returned in 72 hrs. Cited research linked below in replies...

Valerie Anne Smith

46,749 görüntüleme • 7 ay önce

My questions to Chief Minister Devendra Fadnavis ji, Housing Minister Eknath Shinde - एकनाथ शिंदे ji, and SRA CEO Dr. Mahendra Kalyankar: 👉 On what basis was Shiv Infra Vision Properties Pvt. Ltd. appointed as the developer for the massive 38-acre SRA project (Sarvadharmiya SRA CHS and 36 other CHS schemes) in Juhu Gully? 👉 What due process was followed? 👉 What is this firm’s link to a BJP leader? 👉 Was the mandatory 13(2) procedure under the Maharashtra Slum Areas Act completed before changing the developer? 👉 Didn't a majority of the affected SRA societies object to this appointment? These are some of the questions I, along with my colleagues, put directly to SRA CEO Dr. Kalyankar during our meeting today. The SRA, created to safeguard the housing rights of the poor, has today become a den of corruption, brazenly siding with builders and those who wield political influence in the corridors of power. The Juhu Gully project, worth thousands of crores, involves 6,500+ slum dwellers, almost all of whom were kept in the dark before a new developer was imposed upon them. Why were they not consulted? Isn’t this a violation of their rights and the very spirit of the SRA rules? Today, most of them live under the fear of being forcefully displaced and denied their rightful in-situ rehabilitation. At the meeting, I demanded answers to these questions. We will not stop here. We will keep pursuing this case till justice is done. (1/2) #BuilderRaj #CorruptionKiBaat #PeopleVsMitrjiviSarkar #SRA #Mumbai
0:58

My questions to Chief Minister Devendra Fadnavis ji, Housing Minister Eknath Shinde - एकनाथ शिंदे ji, and SRA CEO Dr. Mahendra Kalyankar: 👉 On what basis was Shiv Infra Vision Properties Pvt. Ltd. appointed as the developer for the massive 38-acre SRA project (Sarvadharmiya SRA CHS and 36 other CHS schemes) in Juhu Gully? 👉 What due process was followed? 👉 What is this firm’s link to a BJP leader? 👉 Was the mandatory 13(2) procedure under the Maharashtra Slum Areas Act completed before changing the developer? 👉 Didn't a majority of the affected SRA societies object to this appointment? These are some of the questions I, along with my colleagues, put directly to SRA CEO Dr. Kalyankar during our meeting today. The SRA, created to safeguard the housing rights of the poor, has today become a den of corruption, brazenly siding with builders and those who wield political influence in the corridors of power. The Juhu Gully project, worth thousands of crores, involves 6,500+ slum dwellers, almost all of whom were kept in the dark before a new developer was imposed upon them. Why were they not consulted? Isn’t this a violation of their rights and the very spirit of the SRA rules? Today, most of them live under the fear of being forcefully displaced and denied their rightful in-situ rehabilitation. At the meeting, I demanded answers to these questions. We will not stop here. We will keep pursuing this case till justice is done. (1/2) #BuilderRaj #CorruptionKiBaat #PeopleVsMitrjiviSarkar #SRA #Mumbai

Prof. Varsha Eknath Gaikwad

26,008 görüntüleme • 10 ay önce

🚨🚨🚨 Such an important story! Jan 21, 2024, Full Measure with Sharyl Attkisson (Sharyl Attkisson 🕵️‍♂️💼🥋), Don't forget Pfizer and the FDA tried to bury adverse events! Please watch, forward, email etc. Highlights------------------- Case 1 It's the story of Maddie, one of the children who took part in Pfizer's vaccine study on children. It's a remarkable account of what happened when Maddie got very, very sick, leading to accusations that Pfizer, the FDA and the study leaders tried to bury her case. In summer of 2020, Stephanie De Garay and her family learned an important clinical trial was about to be launched at nearby Cincinnati Children's Hospital. It would test Pfizer's experimental Covid-19 vaccine on 12 to 15 year olds to see if it was safe and effective. The De Garay's firmly pro-vaccine, didn't hesitate to let their children take part. Among three siblings, twelve year old Maddie alone was chosen to get two doses of Pfizer's vaccine, rather than a harmless placebo, it proved a fateful and debilitating roll of the dice. Her second dose was January 20 of 2021. So by the time she came home from school my husband called me at work and said, Maddie's having some sort of reaction. She had what she described as electrical shocks going up and down her spine. she said she felt like her heart was being ripped out. So chest pain, she had severe abdominal pain. She was hunched over when she walked through the door. Her toes and her fingers were white and they were like, when you touched them, they were ice cold and painful. Did you think right away that this was probably a vaccine reaction? "100%." De Garay says she was shocked when the lead study doctor offered no help. "I trusted the government. I trusted doctors. I trusted hospitals.... What I thought they were is not what they are." Case 2 Carrie Peterson Edberg's son Milo got the shot in December of 2021 and ended up with a serious heart problem that's associated with COVID vaccines. He got vaccinated on, like, a Friday. And on Sunday, he actually. Sunday morning at 01:00 a.m. Was on life support. He was diagnosed with myocarditis. doctors, of course, would not say it was vaccine-injured, but why would a six year old have myocarditis? Case 3 Daniel Hartman's 17 year old son was rushed to the hospital four days after his shot in September of 2021. My son Sean played hockey his whole life. To continue to play hockey, he had to get a vaccine. He took one Pfizer shot and died 33 days later. Answers4Sean 🇨🇦 Case 4 And 16 year old Ernesto, son of single parent Ernest Ramirez, dropped dead of an enlarged heart five days after his Pfizer Covid shot. When I got there, they were loading him up in the ambulance. I changed the ambulance to the hospital. When I got there, they were working on him at the hospital. There was a young doctor. He came out, he was. Your son's dead. You can go home. Ernest Ramirez ---------------------------------- Pfizer Cincinnati Children's Hospital and lead study scientist Dr. Robert Frenck declined comment and wouldn't answer our questions. Same with CDC, which also wouldn't tell us how many adverse event reports in children it's received for Covid vaccines. We asked federal health officials if they agree with Pfizer's published claim that, quote, there were no vaccine related serious adverse events in their study on children. But they declined to answer the question.
9:45

🚨🚨🚨 Such an important story! Jan 21, 2024, Full Measure with Sharyl Attkisson (Sharyl Attkisson 🕵️‍♂️💼🥋), Don't forget Pfizer and the FDA tried to bury adverse events! Please watch, forward, email etc. Highlights------------------- Case 1 It's the story of Maddie, one of the children who took part in Pfizer's vaccine study on children. It's a remarkable account of what happened when Maddie got very, very sick, leading to accusations that Pfizer, the FDA and the study leaders tried to bury her case. In summer of 2020, Stephanie De Garay and her family learned an important clinical trial was about to be launched at nearby Cincinnati Children's Hospital. It would test Pfizer's experimental Covid-19 vaccine on 12 to 15 year olds to see if it was safe and effective. The De Garay's firmly pro-vaccine, didn't hesitate to let their children take part. Among three siblings, twelve year old Maddie alone was chosen to get two doses of Pfizer's vaccine, rather than a harmless placebo, it proved a fateful and debilitating roll of the dice. Her second dose was January 20 of 2021. So by the time she came home from school my husband called me at work and said, Maddie's having some sort of reaction. She had what she described as electrical shocks going up and down her spine. she said she felt like her heart was being ripped out. So chest pain, she had severe abdominal pain. She was hunched over when she walked through the door. Her toes and her fingers were white and they were like, when you touched them, they were ice cold and painful. Did you think right away that this was probably a vaccine reaction? "100%." De Garay says she was shocked when the lead study doctor offered no help. "I trusted the government. I trusted doctors. I trusted hospitals.... What I thought they were is not what they are." Case 2 Carrie Peterson Edberg's son Milo got the shot in December of 2021 and ended up with a serious heart problem that's associated with COVID vaccines. He got vaccinated on, like, a Friday. And on Sunday, he actually. Sunday morning at 01:00 a.m. Was on life support. He was diagnosed with myocarditis. doctors, of course, would not say it was vaccine-injured, but why would a six year old have myocarditis? Case 3 Daniel Hartman's 17 year old son was rushed to the hospital four days after his shot in September of 2021. My son Sean played hockey his whole life. To continue to play hockey, he had to get a vaccine. He took one Pfizer shot and died 33 days later. Answers4Sean 🇨🇦 Case 4 And 16 year old Ernesto, son of single parent Ernest Ramirez, dropped dead of an enlarged heart five days after his Pfizer Covid shot. When I got there, they were loading him up in the ambulance. I changed the ambulance to the hospital. When I got there, they were working on him at the hospital. There was a young doctor. He came out, he was. Your son's dead. You can go home. Ernest Ramirez ---------------------------------- Pfizer Cincinnati Children's Hospital and lead study scientist Dr. Robert Frenck declined comment and wouldn't answer our questions. Same with CDC, which also wouldn't tell us how many adverse event reports in children it's received for Covid vaccines. We asked federal health officials if they agree with Pfizer's published claim that, quote, there were no vaccine related serious adverse events in their study on children. But they declined to answer the question.

aussie17

71,777 görüntüleme • 2 yıl önce

Higher deuterium in drinking water correlates with higher rates of major depression. Higher deuterium in drinking water correlates with higher rates of type 2 diabetes. This isn't a fringe hypothesis. It's a University of Utah population study mapping deuterium concentration in US tap water against disease prevalence across the country. Correlation — not proof of causation. But striking enough that Tatyana Strekalova — Clinician Scientist at Maastricht University, Senior Researcher at the University of Oxford, and Professor of Physiology at Sechenov First Moscow State Medical University — decided to test it in mice. The logic is straightforward. Deuterium concentration in drinking water decreases with distance from the ocean — inland, high-altitude water is naturally more deuterium-depleted. If geography determines deuterium load, and deuterium load correlates with disease prevalence, then what happens when you deliberately give animals water at the low end of that natural range? What her lab found is striking. They used 90 ppm deuterium-depleted water throughout — the lowest deuterium concentration found naturally in drinking water on Earth. Not a pharmaceutical dose. Not exotic laboratory depletion. And compared it to control mice drinking 140 ppm water. The difference between antarctic meltwater and coastal tap water. Finding 1: Aged mice. Two weeks. Depressive-like behaviors measurably reduced They took 18-month-old mice — equivalent to very old age, approaching maximum mouse lifespan. These mice displayed measurable depressive behaviors: Anhedonia — loss of sensitivity to reward, measured by reduced preference for sweet water. Increased helplessness behavior. Reduced novelty exploration. Impaired hippocampus-dependent memory. After two weeks on 90 ppm DDW? Sucrose preference increased — anhedonia reversed. Helplessness behavior significantly reduced. Novelty exploration improved. Hippocampal memory improved. Two weeks. Naturally occurring low-deuterium water. Measurable reversal across four independent behavioral markers. Finding 2: DDW matched antidepressant effect in stressed young mice They used a chronic stress model in young mice — predator scent, restraint stress, tail suspension. This reliably induces anhedonia in susceptible mice. Then they divided mice into three groups: normal water at 140 ppm, DDW at 90 ppm, and citalopram — a standard SSRI antidepressant. DDW produced rescue of sucrose preference comparable to citalopram. Helplessness behavior was also rescued comparably. Serotonin transporter expression — one of the key molecular targets of SSRIs — was rescued by both citalopram and DDW. This is mouse data. Direct translation to humans requires clinical trials. But the mechanism convergence is a legitimate finding. Finding 3: DDW normalized REM sleep in stressed mice Depression is the only psychiatric disorder diagnosable by a specific sleep architecture change — increased REM sleep. It's a biological marker, not a subjective report. Stressed mice showed increased REM sleep — the biological depression signature. DDW normalized REM sleep. Slow-wave sleep and wakefulness also improved. Finding 4: DDW protected against western diet-induced cognitive impairment and glucose dysregulation They used 12-month-old female mice on a standardized western diet — high saturated fat, high sugar, high cholesterol. Western diet produced: impaired glucose tolerance, brain inflammation, reduced mitochondrial markers in brain and liver, liver steatosis — fat accumulation in the liver — impaired object recognition memory, and impaired hippocampal memory. DDW at 90 ppm on western diet: Prevented glucose tolerance impairment despite continued western diet. Improved object recognition memory. Improved hippocampal memory in old mice. Did not improve liver steatosis. The liver finding matters. DDW protected the brain and metabolic glucose handling but did not reverse the liver damage. Strekalova’s interpretation: DDW is counteracting brain inflammation driven by damage elsewhere in the body — not fixing the damage itself. Finding 5: Deuterium-enriched water (180 ppm) did the opposite They tested the reverse — 180 ppm water, equivalent to what you would find in evaporative pools in the Sahara. Results on aged mice with western diet: Novelty exploration clearly suppressed. Hippocampus-dependent memory suppressed. Strekalova describes this as a surprise finding. 90 ppm sits at the low end of natural drinking water on Earth. 180 ppm sits at the high end of what occurs in extreme arid environments. The difference between them produced measurable opposing effects on memory and cognition in aged mice. Gene expression — deuterium sits upstream of circadian biology In both the aging model and the stress model, DDW altered gene expression in the hippocampus and prefrontal cortex. Affected categories: DNA repair, oxidative stress response, immune regulation, mitochondrial function, cellular plasticity, aging-related genes. And one finding that connects directly to everything else: Per2. Per2 is a core circadian clock gene. DDW affecting its expression means deuterium content influences circadian biology at the gene level. Deuterium doesn't just affect cancer cells and mitochondrial efficiency. It sits upstream of the circadian system. The implication The deuterium content of your water varies by geography. Antarctic water versus coastal tap water. The difference is measurable. The biological effects in these models are measurable and opposing. Most people optimizing their health are tracking sleep, sunlight, training, and nutrition. Nobody told them deuterium was also on the list.
9:09

Higher deuterium in drinking water correlates with higher rates of major depression. Higher deuterium in drinking water correlates with higher rates of type 2 diabetes. This isn't a fringe hypothesis. It's a University of Utah population study mapping deuterium concentration in US tap water against disease prevalence across the country. Correlation — not proof of causation. But striking enough that Tatyana Strekalova — Clinician Scientist at Maastricht University, Senior Researcher at the University of Oxford, and Professor of Physiology at Sechenov First Moscow State Medical University — decided to test it in mice. The logic is straightforward. Deuterium concentration in drinking water decreases with distance from the ocean — inland, high-altitude water is naturally more deuterium-depleted. If geography determines deuterium load, and deuterium load correlates with disease prevalence, then what happens when you deliberately give animals water at the low end of that natural range? What her lab found is striking. They used 90 ppm deuterium-depleted water throughout — the lowest deuterium concentration found naturally in drinking water on Earth. Not a pharmaceutical dose. Not exotic laboratory depletion. And compared it to control mice drinking 140 ppm water. The difference between antarctic meltwater and coastal tap water. Finding 1: Aged mice. Two weeks. Depressive-like behaviors measurably reduced They took 18-month-old mice — equivalent to very old age, approaching maximum mouse lifespan. These mice displayed measurable depressive behaviors: Anhedonia — loss of sensitivity to reward, measured by reduced preference for sweet water. Increased helplessness behavior. Reduced novelty exploration. Impaired hippocampus-dependent memory. After two weeks on 90 ppm DDW? Sucrose preference increased — anhedonia reversed. Helplessness behavior significantly reduced. Novelty exploration improved. Hippocampal memory improved. Two weeks. Naturally occurring low-deuterium water. Measurable reversal across four independent behavioral markers. Finding 2: DDW matched antidepressant effect in stressed young mice They used a chronic stress model in young mice — predator scent, restraint stress, tail suspension. This reliably induces anhedonia in susceptible mice. Then they divided mice into three groups: normal water at 140 ppm, DDW at 90 ppm, and citalopram — a standard SSRI antidepressant. DDW produced rescue of sucrose preference comparable to citalopram. Helplessness behavior was also rescued comparably. Serotonin transporter expression — one of the key molecular targets of SSRIs — was rescued by both citalopram and DDW. This is mouse data. Direct translation to humans requires clinical trials. But the mechanism convergence is a legitimate finding. Finding 3: DDW normalized REM sleep in stressed mice Depression is the only psychiatric disorder diagnosable by a specific sleep architecture change — increased REM sleep. It's a biological marker, not a subjective report. Stressed mice showed increased REM sleep — the biological depression signature. DDW normalized REM sleep. Slow-wave sleep and wakefulness also improved. Finding 4: DDW protected against western diet-induced cognitive impairment and glucose dysregulation They used 12-month-old female mice on a standardized western diet — high saturated fat, high sugar, high cholesterol. Western diet produced: impaired glucose tolerance, brain inflammation, reduced mitochondrial markers in brain and liver, liver steatosis — fat accumulation in the liver — impaired object recognition memory, and impaired hippocampal memory. DDW at 90 ppm on western diet: Prevented glucose tolerance impairment despite continued western diet. Improved object recognition memory. Improved hippocampal memory in old mice. Did not improve liver steatosis. The liver finding matters. DDW protected the brain and metabolic glucose handling but did not reverse the liver damage. Strekalova’s interpretation: DDW is counteracting brain inflammation driven by damage elsewhere in the body — not fixing the damage itself. Finding 5: Deuterium-enriched water (180 ppm) did the opposite They tested the reverse — 180 ppm water, equivalent to what you would find in evaporative pools in the Sahara. Results on aged mice with western diet: Novelty exploration clearly suppressed. Hippocampus-dependent memory suppressed. Strekalova describes this as a surprise finding. 90 ppm sits at the low end of natural drinking water on Earth. 180 ppm sits at the high end of what occurs in extreme arid environments. The difference between them produced measurable opposing effects on memory and cognition in aged mice. Gene expression — deuterium sits upstream of circadian biology In both the aging model and the stress model, DDW altered gene expression in the hippocampus and prefrontal cortex. Affected categories: DNA repair, oxidative stress response, immune regulation, mitochondrial function, cellular plasticity, aging-related genes. And one finding that connects directly to everything else: Per2. Per2 is a core circadian clock gene. DDW affecting its expression means deuterium content influences circadian biology at the gene level. Deuterium doesn't just affect cancer cells and mitochondrial efficiency. It sits upstream of the circadian system. The implication The deuterium content of your water varies by geography. Antarctic water versus coastal tap water. The difference is measurable. The biological effects in these models are measurable and opposing. Most people optimizing their health are tracking sleep, sunlight, training, and nutrition. Nobody told them deuterium was also on the list.

no.mind

17,170 görüntüleme • 1 ay önce

7 Compelling Reasons Why Ivermectin Is a ‘Powerful Drug’ for Fighting Cancer Ivermectin is often recognized–2nd to penicillin–for having the greatest impact on human health. Its discovery even won the Nobel Prize. It is safer than Tylenol and brought river blindness to the brink of extinction, but the propagandists told you it was a “dangerous horse dewormer.” Well, it now turns out that ivermectin is not only an effective treatment for COVID-19, but it could also be a “powerful drug” for fighting cancer. Here are 7 reasons why. 1. Multiple Anti-Cancer Effects: Ivermectin impacts at least nine well-defined cancer targets, according to Dr. Alfonso Dueñas-González, an oncologist and senior researcher. He states, "There are at least nine perfectly defined cancer targets affected by ivermectin." 2. Enhances Effects of Chemotherapy and Radiation: Ivermectin not only targets tumor stem cells and promotes cancer cell death but also "enhances the effects of chemo and radiation therapy." This broad impact on the immune system increases the offense against cancers, making it a versatile adjunct to conventional treatments. 3. Inhibits Cancer Cell Cycles: The drug prevents the formation of new cancer cells by inhibiting cancer cell cycles and inducing mitochondrial stress, which leads to the killing of cancer cells. This mechanism is crucial for stopping the proliferation of cancerous cells. 4. Prevents Formation of New Blood Vessels Near Cancer Cells: Ivermectin prevents cancer survival by inhibiting the formation of new blood vessels that transport energy and fuel to cancers. This action starves the cancer cells, hindering their growth and spread. 5. Synergizes with Immunotherapy: Dr. Peter P. Lee, chair of immuno-oncology at the City of Hope, found that ivermectin could synergize with immune checkpoint inhibitor anti-PD1, enhancing the body's immune response to fight cancer. "What we’re learning is that ivermectin is going to be a very powerful drug in the context of really carefully developed immunotherapy combinations," he said. 6. Targets Cancer Stem Cells: Ivermectin preferentially targets cancer stem cells, which are a driver of cancer tumors and relapses. By focusing on these cells, ivermectin attacks the root of cancer's resilience and ability to recur. 7. The Curious Case of Rick Alderson: Mr. Alderson, a retired sawmill worker, “was a dead man walking” and given 6 months to live after his terminal colon cancer had metastasized and spread to his liver, where it had formed 25 distinct tumors. After starting ivermectin, Rick Alderson's carcinoembryonic antigen (CEA) levels, which are markers for tumor activity, dropped significantly from 1,498 ng/mL to 13.9 ng/mL in a matter of months. Of the 25 tumors in Mr. Alderson's liver, only three remained after his treatment with ivermectin and chemotherapy, indicating a substantial reduction in tumor burden. Mr. Alderson lived for two more years beyond his initial six-month prognosis, which his wife attributes to the use of ivermectin alongside chemotherapy.
3:43

7 Compelling Reasons Why Ivermectin Is a ‘Powerful Drug’ for Fighting Cancer Ivermectin is often recognized–2nd to penicillin–for having the greatest impact on human health. Its discovery even won the Nobel Prize. It is safer than Tylenol and brought river blindness to the brink of extinction, but the propagandists told you it was a “dangerous horse dewormer.” Well, it now turns out that ivermectin is not only an effective treatment for COVID-19, but it could also be a “powerful drug” for fighting cancer. Here are 7 reasons why. 1. Multiple Anti-Cancer Effects: Ivermectin impacts at least nine well-defined cancer targets, according to Dr. Alfonso Dueñas-González, an oncologist and senior researcher. He states, "There are at least nine perfectly defined cancer targets affected by ivermectin." 2. Enhances Effects of Chemotherapy and Radiation: Ivermectin not only targets tumor stem cells and promotes cancer cell death but also "enhances the effects of chemo and radiation therapy." This broad impact on the immune system increases the offense against cancers, making it a versatile adjunct to conventional treatments. 3. Inhibits Cancer Cell Cycles: The drug prevents the formation of new cancer cells by inhibiting cancer cell cycles and inducing mitochondrial stress, which leads to the killing of cancer cells. This mechanism is crucial for stopping the proliferation of cancerous cells. 4. Prevents Formation of New Blood Vessels Near Cancer Cells: Ivermectin prevents cancer survival by inhibiting the formation of new blood vessels that transport energy and fuel to cancers. This action starves the cancer cells, hindering their growth and spread. 5. Synergizes with Immunotherapy: Dr. Peter P. Lee, chair of immuno-oncology at the City of Hope, found that ivermectin could synergize with immune checkpoint inhibitor anti-PD1, enhancing the body's immune response to fight cancer. "What we’re learning is that ivermectin is going to be a very powerful drug in the context of really carefully developed immunotherapy combinations," he said. 6. Targets Cancer Stem Cells: Ivermectin preferentially targets cancer stem cells, which are a driver of cancer tumors and relapses. By focusing on these cells, ivermectin attacks the root of cancer's resilience and ability to recur. 7. The Curious Case of Rick Alderson: Mr. Alderson, a retired sawmill worker, “was a dead man walking” and given 6 months to live after his terminal colon cancer had metastasized and spread to his liver, where it had formed 25 distinct tumors. After starting ivermectin, Rick Alderson's carcinoembryonic antigen (CEA) levels, which are markers for tumor activity, dropped significantly from 1,498 ng/mL to 13.9 ng/mL in a matter of months. Of the 25 tumors in Mr. Alderson's liver, only three remained after his treatment with ivermectin and chemotherapy, indicating a substantial reduction in tumor burden. Mr. Alderson lived for two more years beyond his initial six-month prognosis, which his wife attributes to the use of ivermectin alongside chemotherapy.

The Vigilant Fox 🦊

532,851 görüntüleme • 2 yıl önce

This is undoubtedly one of the most extraordinary interviews of a former senior US government official on Gaza. This is Chas Freeman, former Assistant Secretary of Defense and former US Ambassador to Saudi Arabia. Key points in the video: - He agrees that many of the victims of Oct 7th were killed by the Israeli army in the form of "undisciplined fire by helicopters with hellfire missiles or by tanks with incendiary rounds directed at buildings". In the case of the victims of the music festival he even says they "were largely killed, it appears, by hellfire missiles and by other undisciplined fire by Israeli forces". To him this "disgrace in military terms" stems from a "lack of discipline and training necessary to respond" but also from the IDF's "Hannibal directive", which "says that rather than get into bargaining over hostage exchange you should just kill the Israeli hostages along with their captors." - He says that with Oct 7th "Hamas had 2 objectives": 1) "Put the Palestinian self-determination issue back on the global agenda", something he says they've "succeeded" in doing since they're is "widespread recognition outside Israel that only self-determination for Palestine in the form of a 2-state solution can provide security to Israel". He says that even in "the US, which has a larger Jewish population than Israel, many Jews have come to realize that this is the case. Younger Jews in particular in the U.S. are very disillusioned with Zionism and don't want to suffer contagion from it in the form of antisemitism, which is actually growing now as a result of Israeli actions". 2) "Give Hamas enormous popularity among Palestinians because they are seen as having stood up, as having been willing to accept death rather than captivity". He refers to Norman Finkelstein's "analogy of slave revolts in the U.S." and particularly the "1831 revolt by Nat Turner, a well-educated very intelligent enslaved African who led a slave revolt in Southern Virginia which had as its objective the murder of every white person they encountered." He says it "raises a moral question: 'Is the violence of the slave-owner morally the same as the violence of the slave trying to end that violence?'. The same moral question arises with Israeli oppression of Palestinians versus Palestinian resistance to oppression." - All in all he concludes that much like the violence against African-Americans that followed slave revolts in the 19th century, the Israeli vengeance against Palestinians "won't be remembered fondly by anyone in the future". In fact he goes as far as saying that "when people think of Israel in the past they thought of it as a refuge for the victims of the Holocaust... now they will think of it as the home of perpetrators of genocide. When they think of Israel, they will think of burned buildings and dead babies. This is an image problem of a fundamental nature and from the point of view of Israel it strips Israel of its protection by charges of antisemitism against anyone who is critical of Israel because to be critical of people who are carrying out genocide cannot be antisemitism, it cannot be considered immoral. Antisemitism is a despicable attitude but to oppose genocide by Israel is not."
7:55

This is undoubtedly one of the most extraordinary interviews of a former senior US government official on Gaza. This is Chas Freeman, former Assistant Secretary of Defense and former US Ambassador to Saudi Arabia. Key points in the video: - He agrees that many of the victims of Oct 7th were killed by the Israeli army in the form of "undisciplined fire by helicopters with hellfire missiles or by tanks with incendiary rounds directed at buildings". In the case of the victims of the music festival he even says they "were largely killed, it appears, by hellfire missiles and by other undisciplined fire by Israeli forces". To him this "disgrace in military terms" stems from a "lack of discipline and training necessary to respond" but also from the IDF's "Hannibal directive", which "says that rather than get into bargaining over hostage exchange you should just kill the Israeli hostages along with their captors." - He says that with Oct 7th "Hamas had 2 objectives": 1) "Put the Palestinian self-determination issue back on the global agenda", something he says they've "succeeded" in doing since they're is "widespread recognition outside Israel that only self-determination for Palestine in the form of a 2-state solution can provide security to Israel". He says that even in "the US, which has a larger Jewish population than Israel, many Jews have come to realize that this is the case. Younger Jews in particular in the U.S. are very disillusioned with Zionism and don't want to suffer contagion from it in the form of antisemitism, which is actually growing now as a result of Israeli actions". 2) "Give Hamas enormous popularity among Palestinians because they are seen as having stood up, as having been willing to accept death rather than captivity". He refers to Norman Finkelstein's "analogy of slave revolts in the U.S." and particularly the "1831 revolt by Nat Turner, a well-educated very intelligent enslaved African who led a slave revolt in Southern Virginia which had as its objective the murder of every white person they encountered." He says it "raises a moral question: 'Is the violence of the slave-owner morally the same as the violence of the slave trying to end that violence?'. The same moral question arises with Israeli oppression of Palestinians versus Palestinian resistance to oppression." - All in all he concludes that much like the violence against African-Americans that followed slave revolts in the 19th century, the Israeli vengeance against Palestinians "won't be remembered fondly by anyone in the future". In fact he goes as far as saying that "when people think of Israel in the past they thought of it as a refuge for the victims of the Holocaust... now they will think of it as the home of perpetrators of genocide. When they think of Israel, they will think of burned buildings and dead babies. This is an image problem of a fundamental nature and from the point of view of Israel it strips Israel of its protection by charges of antisemitism against anyone who is critical of Israel because to be critical of people who are carrying out genocide cannot be antisemitism, it cannot be considered immoral. Antisemitism is a despicable attitude but to oppose genocide by Israel is not."

Arnaud Bertrand

2,185,170 görüntüleme • 2 yıl önce

Positioning of drugs in Crohn's disease ___ 1. Start effective therapy early This means at diagnosis in the vast majority of patients. Don’t make patients earn their way onto an effective drug. And use your best drug first. Please do not “save it in case you need it later”. ___ 2. Which of our effective therapies should you start? This matters less that just starting. Think holistically with a patient-centered approach. Age, co-morbidities, extra-intestinal manifestations, pregnancy, etc all important. Consider efficacy - speed of onset, mucosal healing, durability of remission - and safety. Mode of delivery - intravenous, subcutaneous, oral - is important. But comes after patient factors, efficacy and safety. Access issues will predominate for many. Use what you have. Use what you know. Just use an effective drug. ___ 3. Use a treat-to-target approach Without labouring the points around STRIDE-2, I’ll put it very simply: - monitor, monitor, monitor act on the results of the monitoring. Don’t keep going with a therapy that isn’t working. ___ 4. Know when to dose optimise versus switch Optimising anti-TNF is often a good ploy. But do it properly and don’t wait too long. Double the dose, shorten the frequency and wait 2-3 cycles. If it isn’t working then (objectively), switch out of class. With ustekinumab, I would no longer dose optimise, but rather switch a partial responder to risankizumab. ___ 5. Active disease is more dangerous than any drugs Two bits of data this year show this: i) In Profile, patients in the step-up group had twice as many adverse events as those in the top-down group. Most of this was because of flaring Crohn’s disease - including hospitalisations for severe disease - but there were also fewer serious infections in the top down group. And that was with combination infliximab and azathioprine. ii) Two meta-analyses of the harms from placebo in RCT’s show a very clear signal. Active Crohn’s disease and UC, when left untreated for even a number of week, is associated with increased toxicity. More on this later. ___ 6. Avoid steroids The majority of patients with Crohn’s disease can be managed effectively now without steroids. They will still have a role in sick patients, to bridge to some therapies, and a course of budesonide in mild to moderate ileal Crohn’s disease is often useful. However we have better strategies now, including using JAK inhibitors in place of steroids. We are increasingly using a short course to (re)capture response to a biologic or keeping the JAKi going in combination at a low dose. ___ 7. Other treatment modalities Surgery and nutritional therapy are particularly important. ___ 8. Changing the natural history of Crohn’s disease Disease modification is the end result when following these principles. We see it in the Edinburgh IBD clinic. A decade since we switched to a top-down strategy for Crohn’s disease and our patients have better disease control, less surgery and fewer hospitalisations. Clearly we still have work to do, but this is major progress.
4:55

Positioning of drugs in Crohn's disease ___ 1. Start effective therapy early This means at diagnosis in the vast majority of patients. Don’t make patients earn their way onto an effective drug. And use your best drug first. Please do not “save it in case you need it later”. ___ 2. Which of our effective therapies should you start? This matters less that just starting. Think holistically with a patient-centered approach. Age, co-morbidities, extra-intestinal manifestations, pregnancy, etc all important. Consider efficacy - speed of onset, mucosal healing, durability of remission - and safety. Mode of delivery - intravenous, subcutaneous, oral - is important. But comes after patient factors, efficacy and safety. Access issues will predominate for many. Use what you have. Use what you know. Just use an effective drug. ___ 3. Use a treat-to-target approach Without labouring the points around STRIDE-2, I’ll put it very simply: - monitor, monitor, monitor act on the results of the monitoring. Don’t keep going with a therapy that isn’t working. ___ 4. Know when to dose optimise versus switch Optimising anti-TNF is often a good ploy. But do it properly and don’t wait too long. Double the dose, shorten the frequency and wait 2-3 cycles. If it isn’t working then (objectively), switch out of class. With ustekinumab, I would no longer dose optimise, but rather switch a partial responder to risankizumab. ___ 5. Active disease is more dangerous than any drugs Two bits of data this year show this: i) In Profile, patients in the step-up group had twice as many adverse events as those in the top-down group. Most of this was because of flaring Crohn’s disease - including hospitalisations for severe disease - but there were also fewer serious infections in the top down group. And that was with combination infliximab and azathioprine. ii) Two meta-analyses of the harms from placebo in RCT’s show a very clear signal. Active Crohn’s disease and UC, when left untreated for even a number of week, is associated with increased toxicity. More on this later. ___ 6. Avoid steroids The majority of patients with Crohn’s disease can be managed effectively now without steroids. They will still have a role in sick patients, to bridge to some therapies, and a course of budesonide in mild to moderate ileal Crohn’s disease is often useful. However we have better strategies now, including using JAK inhibitors in place of steroids. We are increasingly using a short course to (re)capture response to a biologic or keeping the JAKi going in combination at a low dose. ___ 7. Other treatment modalities Surgery and nutritional therapy are particularly important. ___ 8. Changing the natural history of Crohn’s disease Disease modification is the end result when following these principles. We see it in the Edinburgh IBD clinic. A decade since we switched to a top-down strategy for Crohn’s disease and our patients have better disease control, less surgery and fewer hospitalisations. Clearly we still have work to do, but this is major progress.

Charlie Lees

15,650 görüntüleme • 1 yıl önce

⏰ THE MOST BANNED THREAD IN THE WORLD! 🚨 The War On Resonance PART FIVE: The Final Sterilization Protocol IGNORANCE IS NO LONGER ACCEPTABLE! If this knowledge is not received, remembered, and shared; THE HUMAN RACE WILL CEASE TO EXIST. THE CHOICE IS NOW YOURS. They knew they couldn’t kill God. So instead... they tried to kill the memory of God inside of you. What began as a quiet experiment in infertility has become a planetary extinction protocol: not by bombs or bullets, but by signal, by consent, by silence. And if you want to understand how they plan to delete the human soul... forever; you need to know where they’ve hidden the final mechanisms. They’re not in war zones anymore. They’re in your kitchen, your classroom, your air supply... in the very places you were taught to trust. Let me take you there. ☠️ THE KILL SWITCH MENU: FOOD AS A WEAPONIZED DELIVERY SYSTEM The next phase of biological sterilization is now hidden in your plate, your pantry, your packaging. This is not speculation; it’s embedded in patents and production protocols: Lipid Nanoparticle Contamination in Global Food Supply Pfizer’s own biodistribution studies show rapid ovarian accumulation. Now, the same LNP structures are being sprayed onto crops via mRNA “edible vaccines”, falsely labeled as “climate-resilient biotech.” Edible Vaccines "One day children may get immunized by munching on foods instead of enduring shots. More important, food vaccines might save millions who now die for lack of access to traditional inoculants" 🔗 Digital University Aula in Nanotechnology education to fight COVID 19 Nano-Code 🔗 Pfizer LNP Biodistribution Study - Page 16 🔗 Pfizer/BioNTech COVID-19 mRNA vaccine (BNT162, PF-07302048) TGA Pre-Submission Meeting September 18, 2020 🔗 Brand Name Comirnaty Intramuscular Injection Non-proprietary Name Coronavirus Modified Uridine RNA Vaccine (SARS-CoV-2) (Active ingredient: Tozinameran [JAN*]) Applicant Pfizer Japan Inc. Date of Application December 18, 2020 Table 1 Pharmacokinetics of LUCIFERase RNA-encapsulated LNPs, ALC-0315 and ALC0159, when administered intravenously to Wistar Han rats at a dose of 1 mg RNA/kg..... 4 LIST OF FIGURES Figure 1 Plasma and liver concentrations of ALC-0315 and ALC-0159 after intravenous administration of LUCIFERase RNA-encapsulated LNPs at a dose of 1 mg RNA/kg to Wistar Han rats..... 5 Figure 2 In vivo luminescence in BALB/c mice intramuscularly treated with LUCIFERase RNA-encapsulated LNP..... 6 Figure 3 Estimated in vivo metabolic pathways of ALC-0315 in various animal species..8 Figure 4 Estimated in vivo metabolic pathways of ALC-0159 in various animal species. 9 🔗 🔗 Biodistribution of RNA Vaccines and of Their Products: Evidence from Human and Animal Studies 🔗 Nonclinical Evaluation Report BNT162b2 [mRNA] COVID-19 vaccine (COMIRNATYTM) Submission No: PM-2020-05461-1-2 Sponsor: Pfizer Australia Pty Ltd January 2021 🔗 Luciferase mRNA Transfection of Antigen Presenting Cells Permits Sensitive Nonradioactive Measurement of Cellular and Humoral Cytotoxicity 🔗 CRISPR-Edited Meat and Produce Companies like Ginkgo Bioworks, funded by DARPA and the Gates Foundation, are engineering DNA-edited livestock and grains that introduce heritable gene silencing traits through ingestion. These payloads are not just physical. They are frequency-coded to activate upon specific satellite signals from the 5G grid. You’re not just being poisoned. You’re being programmed... by dinner. CRISPR Food Industry Mapping How Helpful May Be a CRISPR/Cas-Based System for Food Traceability? 🔗 Adoption of CRISPR-Cas for crop production: present status and future prospects 🔗 Crop bioengineering via gene editing: reshaping the future of agriculture 🔗 CRISPR/Cas genome editing system and its application in potato 🔗 Analysis of the Utilization and Prospects of CRISPR-Cas Technology in the Annotation of Gene Function and Creation New Germplasm in Maize Based on Patent Data 🔗 CRISPR/Cas9 Technology and Its Utility for Crop Improvement 🔗 CRISPR-Based Genome Editing for Nutrient Enrichment in Crops: A Promising Approach Toward Global Food Security 🔗 Mechanism and Applications of CRISPR/Cas-9-Mediated Genome Editing 🔗 Application of CRISPR/Cas9 in Crop Quality Improvement 🔗 Recent Advances in the Application of CRISPR/Cas9 Gene Editing System in Poultry Species 🔗 Mapping CRISPR-Cas9 public and commercial innovation using The Lens institutional toolkit 🔗 How Helpful May Be a CRISPR/Cas-Based System for Food Traceability? 🔗 A Critical Review: Recent Advancements in the Use of CRISPR/Cas9 Technology to Enhance Crops and Alleviate Global Food Crises 🔗 Application of CRISPR-Cas9 genome editing technology in various fields: A review 🔗 A technological and regulatory outlook on CRISPR crop editing 🔗 Theragnostic application of nanoparticle and CRISPR against food-borne multi-drug resistant pathogens 🔗 Recent Advances of CRISPR/Cas9-Based Genetic Engineering and Transcriptional Regulation in Industrial Biology 🔗 Genome-Editing Products Line up for the Market: Will Europe Harvest the Benefits from Science and Innovation? 🔗 Rest assured... I HAVE THE EVIDENCE, I AM FILING SUBPOENAS AND JUSTICE WILL BE SERVED! CONTINUED IN COMMENTS BELOW, REACHED MAXIMUM AMOUNT OF LINKS ALLOWED 👇
7:17

⏰ THE MOST BANNED THREAD IN THE WORLD! 🚨 The War On Resonance PART FIVE: The Final Sterilization Protocol IGNORANCE IS NO LONGER ACCEPTABLE! If this knowledge is not received, remembered, and shared; THE HUMAN RACE WILL CEASE TO EXIST. THE CHOICE IS NOW YOURS. They knew they couldn’t kill God. So instead... they tried to kill the memory of God inside of you. What began as a quiet experiment in infertility has become a planetary extinction protocol: not by bombs or bullets, but by signal, by consent, by silence. And if you want to understand how they plan to delete the human soul... forever; you need to know where they’ve hidden the final mechanisms. They’re not in war zones anymore. They’re in your kitchen, your classroom, your air supply... in the very places you were taught to trust. Let me take you there. ☠️ THE KILL SWITCH MENU: FOOD AS A WEAPONIZED DELIVERY SYSTEM The next phase of biological sterilization is now hidden in your plate, your pantry, your packaging. This is not speculation; it’s embedded in patents and production protocols: Lipid Nanoparticle Contamination in Global Food Supply Pfizer’s own biodistribution studies show rapid ovarian accumulation. Now, the same LNP structures are being sprayed onto crops via mRNA “edible vaccines”, falsely labeled as “climate-resilient biotech.” Edible Vaccines "One day children may get immunized by munching on foods instead of enduring shots. More important, food vaccines might save millions who now die for lack of access to traditional inoculants" 🔗 Digital University Aula in Nanotechnology education to fight COVID 19 Nano-Code 🔗 Pfizer LNP Biodistribution Study - Page 16 🔗 Pfizer/BioNTech COVID-19 mRNA vaccine (BNT162, PF-07302048) TGA Pre-Submission Meeting September 18, 2020 🔗 Brand Name Comirnaty Intramuscular Injection Non-proprietary Name Coronavirus Modified Uridine RNA Vaccine (SARS-CoV-2) (Active ingredient: Tozinameran [JAN*]) Applicant Pfizer Japan Inc. Date of Application December 18, 2020 Table 1 Pharmacokinetics of LUCIFERase RNA-encapsulated LNPs, ALC-0315 and ALC0159, when administered intravenously to Wistar Han rats at a dose of 1 mg RNA/kg..... 4 LIST OF FIGURES Figure 1 Plasma and liver concentrations of ALC-0315 and ALC-0159 after intravenous administration of LUCIFERase RNA-encapsulated LNPs at a dose of 1 mg RNA/kg to Wistar Han rats..... 5 Figure 2 In vivo luminescence in BALB/c mice intramuscularly treated with LUCIFERase RNA-encapsulated LNP..... 6 Figure 3 Estimated in vivo metabolic pathways of ALC-0315 in various animal species..8 Figure 4 Estimated in vivo metabolic pathways of ALC-0159 in various animal species. 9 🔗 🔗 Biodistribution of RNA Vaccines and of Their Products: Evidence from Human and Animal Studies 🔗 Nonclinical Evaluation Report BNT162b2 [mRNA] COVID-19 vaccine (COMIRNATYTM) Submission No: PM-2020-05461-1-2 Sponsor: Pfizer Australia Pty Ltd January 2021 🔗 Luciferase mRNA Transfection of Antigen Presenting Cells Permits Sensitive Nonradioactive Measurement of Cellular and Humoral Cytotoxicity 🔗 CRISPR-Edited Meat and Produce Companies like Ginkgo Bioworks, funded by DARPA and the Gates Foundation, are engineering DNA-edited livestock and grains that introduce heritable gene silencing traits through ingestion. These payloads are not just physical. They are frequency-coded to activate upon specific satellite signals from the 5G grid. You’re not just being poisoned. You’re being programmed... by dinner. CRISPR Food Industry Mapping How Helpful May Be a CRISPR/Cas-Based System for Food Traceability? 🔗 Adoption of CRISPR-Cas for crop production: present status and future prospects 🔗 Crop bioengineering via gene editing: reshaping the future of agriculture 🔗 CRISPR/Cas genome editing system and its application in potato 🔗 Analysis of the Utilization and Prospects of CRISPR-Cas Technology in the Annotation of Gene Function and Creation New Germplasm in Maize Based on Patent Data 🔗 CRISPR/Cas9 Technology and Its Utility for Crop Improvement 🔗 CRISPR-Based Genome Editing for Nutrient Enrichment in Crops: A Promising Approach Toward Global Food Security 🔗 Mechanism and Applications of CRISPR/Cas-9-Mediated Genome Editing 🔗 Application of CRISPR/Cas9 in Crop Quality Improvement 🔗 Recent Advances in the Application of CRISPR/Cas9 Gene Editing System in Poultry Species 🔗 Mapping CRISPR-Cas9 public and commercial innovation using The Lens institutional toolkit 🔗 How Helpful May Be a CRISPR/Cas-Based System for Food Traceability? 🔗 A Critical Review: Recent Advancements in the Use of CRISPR/Cas9 Technology to Enhance Crops and Alleviate Global Food Crises 🔗 Application of CRISPR-Cas9 genome editing technology in various fields: A review 🔗 A technological and regulatory outlook on CRISPR crop editing 🔗 Theragnostic application of nanoparticle and CRISPR against food-borne multi-drug resistant pathogens 🔗 Recent Advances of CRISPR/Cas9-Based Genetic Engineering and Transcriptional Regulation in Industrial Biology 🔗 Genome-Editing Products Line up for the Market: Will Europe Harvest the Benefits from Science and Innovation? 🔗 Rest assured... I HAVE THE EVIDENCE, I AM FILING SUBPOENAS AND JUSTICE WILL BE SERVED! CONTINUED IN COMMENTS BELOW, REACHED MAXIMUM AMOUNT OF LINKS ALLOWED 👇

Noah B. Price

152,192 görüntüleme • 1 yıl önce

I'm up late with the rest of you building AI agents with the new AI browser from Genspark. We can see where this is all going: a new kind of operating system -- one that is very different than the Microsoft centric way that I've been working for 20 years. There are several things that these new agentic browsers bring to you: 1. They let you change how you browse. With an old browser like Google Chrome, you go to your email, Facebook, or X. 2. With these new browsers, you tell it where to go and what to do for you. 3. It can even build software for you. At the end of this video, I have it building me a little YouTube uploading utility, which is very helpful. 4. They have a ton of "applications" built in. Think of it as a new kind of office suite. Docs. Spreadsheets. Slide decks. And much more. All built with AI, not bolted on the side like with Microsoft's Office. 5. They have AI models built "underneath" so you can work privately and cheaply. There’s a lot of new choices you have to make with browsers like this. I’ve been playing with a bunch of them. Some have better user interfaces than others. Some have different versions, slide components, or applications. The reason I like Genspark is because they ship so fast. I’ve been watching this company since its very beginnings, and every week they ship new things. Just yesterday, they shipped a new photo editing feature for my iPhone. I upload a photo and then I can just talk to it and edit it with my voice. It's really cool. I try to reward companies that ship at such a fast rate and that are shipping innovation that improves our lives. It's not that I'm going to stop using Google Chrome. My whole life has been there for, I don't know, almost 20 years now. This is a different way of working and it gives me a space to run my AI tasks that's different than Google Chrome. I run them side by side. One doing old stuff, one doing new stuff. I can keep using Google Chrome for my old stuff, like my email and my calendar. And I use GenSpark or one of the new AI browsers to do new AI-centric things. All sorts of new things that these new agentic browsers open up! Have you tried it, or one of the other new ones yet? How has it changed your work? It takes a little time to get used to AI-centric ways of doing things. Pretend your browser is a team of interns. Give them a task, in this case I said "help me upload my videos to YouTube." You might be shocked at what Genspark does to improve your life. I am everytime I use it. Give it a try and let me know what you think! Oh, and I used another little tool to "write" this post. Typeless -- I push a button and talk and it writes. With fewer typos than I usually type in, to boot. It works great with Genspark's new browser too. Download it here:
3:41

I'm up late with the rest of you building AI agents with the new AI browser from Genspark. We can see where this is all going: a new kind of operating system -- one that is very different than the Microsoft centric way that I've been working for 20 years. There are several things that these new agentic browsers bring to you: 1. They let you change how you browse. With an old browser like Google Chrome, you go to your email, Facebook, or X. 2. With these new browsers, you tell it where to go and what to do for you. 3. It can even build software for you. At the end of this video, I have it building me a little YouTube uploading utility, which is very helpful. 4. They have a ton of "applications" built in. Think of it as a new kind of office suite. Docs. Spreadsheets. Slide decks. And much more. All built with AI, not bolted on the side like with Microsoft's Office. 5. They have AI models built "underneath" so you can work privately and cheaply. There’s a lot of new choices you have to make with browsers like this. I’ve been playing with a bunch of them. Some have better user interfaces than others. Some have different versions, slide components, or applications. The reason I like Genspark is because they ship so fast. I’ve been watching this company since its very beginnings, and every week they ship new things. Just yesterday, they shipped a new photo editing feature for my iPhone. I upload a photo and then I can just talk to it and edit it with my voice. It's really cool. I try to reward companies that ship at such a fast rate and that are shipping innovation that improves our lives. It's not that I'm going to stop using Google Chrome. My whole life has been there for, I don't know, almost 20 years now. This is a different way of working and it gives me a space to run my AI tasks that's different than Google Chrome. I run them side by side. One doing old stuff, one doing new stuff. I can keep using Google Chrome for my old stuff, like my email and my calendar. And I use GenSpark or one of the new AI browsers to do new AI-centric things. All sorts of new things that these new agentic browsers open up! Have you tried it, or one of the other new ones yet? How has it changed your work? It takes a little time to get used to AI-centric ways of doing things. Pretend your browser is a team of interns. Give them a task, in this case I said "help me upload my videos to YouTube." You might be shocked at what Genspark does to improve your life. I am everytime I use it. Give it a try and let me know what you think! Oh, and I used another little tool to "write" this post. Typeless -- I push a button and talk and it writes. With fewer typos than I usually type in, to boot. It works great with Genspark's new browser too. Download it here:

Robert Scoble

70,991 görüntüleme • 10 ay önce