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  • Health benefits of the Sun: Vitamin D can reduce the risk of cancer by as much as 67%
    Rhoda WilsonDecember 28, 2023
    Vitamin D is involved in the biology of all cells in your body, including your immune cells. A large number of studies have shown raising your vitamin D level can significantly reduce your risk of cancer.

    Most recently, researchers found vitamin D and calcium supplementation lowered participants’ overall cancer risk by 30%.

    Having a serum vitamin D level of at least 40 ng/ml reduces your risk for cancer by 67% compared to having a level of 20 ng/ml or less; most cancers occur in people with a vitamin D level between 10 and 40 ng/ml.

    Higher Vitamin D Levels Lower Cancer Risk

    By Dr. Joseph Mercola

    This article was originally published on 10 April 2017.

    Thousands of studies have been done on the health effects of vitamin D, and research shows it is involved in the biology of all cells and tissues in your body, including your immune cells. Your cells actually need the active form of vitamin D to gain access to the genetic blueprints stored inside.

    This is one of the reasons why vitamin D has the ability to impact such a wide variety of health problems – from foetal development to cancer. Unfortunately, despite being easy and inexpensive to address, vitamin D deficiency is an epidemic around the world.

    It’s been estimated that as many as 90% of pregnant mothers and newborns in the sunny Mediterranean region are even deficient in vitamin D,1 thanks to chronic Sun avoidance. A simple mathematical error may also deter many Americans and Canadians from optimising their vitamin D.

    The Institute of Medicine (“IOM”) recommends a mere 600 IUs of vitamin D per day for adults. As pointed out in a 2014 paper,2 the IOM underestimates the need by a factor of 10 due to a mathematical error, which has never been corrected.

    Grassroots Health has created a petition for the IOM and Health Canada to re-evaluate its vitamin D guidelines and correct this mathematical error.3 You can help further this important cause by signing the petition on ipetitions.com.

    More recent research 4 suggests it would require 9,600 IUs of vitamin D per day to get a majority (97.5%) of the population to reach 40 nanograms per millilitre (ng/ml). The American Medical Association uses of 20 ng/ml as sufficient, but research shows 40 ng/mL should be the cutoff point for sufficiency in order to prevent a wide range of diseases, including cancer.

    Research Again Concludes Vitamin D Lowers Cancer Risk

    A large number of studies have shown raising your vitamin D level can significantly reduce your risk of cancer.

    Most recently, a randomised clinical trial 5 by researchers at Creighton University, funded by the National Institutes of Health (“NIH”), found vitamin D and calcium supplementation lowered participants’ overall cancer risk by 30%.6,7,8

    The study, which included more than 2,300 postmenopausal women from Nebraska who were followed for four years, looked at the effects of vitamin D supplementation on all types of cancer.

    Participants were randomly assigned to receive either 2,000 IUs of vitamin D3 in combination with 1,500 mg of calcium, or a placebo for the duration of the study. Blood testing revealed that 25-hydroxyvitamin D (25(OH)D) levels were significantly lower in those who did develop cancer.

    Joan Lappe, Ph.D., professor of nursing and associate dean of research at Creighton University’s College of Nursing, and lead author of the study, said:

    The study provides evidence that higher concentrations of 25(OH)D in the blood, in the context of vitamin D3 and calcium supplementation, decrease risk of cancer … While people can make their own vitamin D3 when they are in the Sun near mid-day, sunscreen blocks most vitamin D production.

    Also, due to more time spent indoors, many individuals lack adequate levels of vitamin D compounds in their blood. The results of this study lend credence to a call for more attention to the importance of vitamin D in human health and specifically in preventing cancer.

    Vitamin D Status Is Strongly Correlated with Cancer Risk

    Previous research has shown that once you reach a serum vitamin D level of 40 ng/ml, your risk for cancer diminishes by 67%, compared to having a level of 20 ng/ml or less.9,10,11,12,13,14,15

    Most cancers, they found, occurred in people with a vitamin D blood level between 10 and 40 ng/ml. The optimal level for cancer protection was identified as being between 40 and 60 ng/ml. Another study 16 published in 2015 found women with vitamin D concentrations of at least 30 ng/ml had a 55% lower risk of colorectal cancer than those who had a blood level below 18 ng/ml.

    Even earlier research, 17 published in 2005, showed women with vitamin D levels above 60 ng/ml had an 83% lower risk of breast cancer than those with levels below 20 ng/ml! The Health and Medicine Division of the National Academies of Sciences, Engineering and Medicine (formerly IOM) has also reported an association between vitamin D and overall mortality risk from all causes, including cancer.18,19

    Vitamin D also increases your chances of surviving cancer if you do get it,20,21 and this includes melanoma. 22

    Access Sun Exposure as Much as Possible and Get Your Vitamin D Level Checked

    The UVB in sunlight is what triggers your body to produce vitamin D. I firmly believe getting regular, sensible Sun exposure is the ideal way to not only optimise your vitamin D level but maximise your health as well because sunlight also has many other important health functions. I’ll review some of these in another section below.

    Regular Sun exposure provides over 1,500 different wavelengths, and we’re just now rediscovering the value of many of these other wavelengths besides UVA and UVB. For example, we now know that red and infrared light helps your body form structured water, which is important for cellular function.

    Many do not appreciate that red, near, mid and far-infrared have many important biological functions. One of them is to improve mitochondrial function, especially the 660 nm and 830 nm wavelengths, as cytochrome C oxidase in mitochondria uses these wavelengths to produce ATP more efficiently.

    Vitamin D3 supplements are a poor second resort, but if you’re unable to get sufficient Sun exposure, then it’s better than nothing. As demonstrated in the featured study – which specifically looked at the effects of supplementation – they do have some benefits.

    Also, while not addressed in this study, I strongly recommend taking your vitamin D3 with vitamin K2 and magnesium as well, since all three work in tandem. A primary consideration when it comes to vitamin D is to get your level checked, ideally twice a year, in the middle of the summer and winter, when your level is at its highest and lowest.

    What you’re aiming for is a level between 40 and 60 ng/ml year-round. Grassroots Health offers vitamin D testing at a great value through its D*Action study.

    Read more: Harness the Power of the Sun for Health (Infographic)

    How to Minimise Your Risk of Skin Cancer from Sun Exposure

    Many avoid Sun exposure for fear of melanoma, an aggressive and potentially lethal form of skin cancer. However, it’s important to realise that melanoma occurs among those with minimal Sun exposure as well.

    An important risk factor for melanoma is overexposure to UV radiation. Baking in the Sun for hours on end on a weekend here and there is not a wise choice.

    To minimise your skin cancer risk, you want to avoid sunburn at all costs. If you’re going to the beach, bring long-sleeved cover-ups and a wide-brimmed hat, and cover up as soon as your skin starts to turn pink.

    Following are some general guidelines for sensible Sun exposure. If you pay close attention to these, you can determine, within reason, safe exposure durations.

    Know your skin type based on the Fitzpatrick skin type classification system. The lighter your skin, the less exposure to UV light is necessary. The downside is that lighter skin is also the most vulnerable to damage from overexposure.
    For very fair-skinned people and those with photodermatitis, any Sun exposure may be unwanted and they should carefully measure vitamin D levels while ensuring they have an adequate intake of vitamin D, vitamin K2, magnesium and calcium.
    For most people, safe UV exposure is possible by knowing your skin type and the current strength of the Sun’s rays. There are several apps and devices to help you optimise the benefits of Sun exposure while mitigating the risks. Also, be extremely careful if you have not been in the Sun for some time. Your first exposures of the year are the most sensitive, so be especially careful to limit your initial time in the Sun.
    Vitamin D Influences Your Health in Many Ways

    The benefits of vitamin D are not restricted to cancer prevention. In fact, the list of health benefits of vitamin D is exceedingly long. As noted earlier, researchers have now realised that vitamin D affects virtually every cell and tissue in your body, so it might be easier to list what it will not affect, rather than what it will impact.

    Compelling evidence suggests that optimising your vitamin D can reduce your risk of death from any cause, 23 making it a foundational component of optimal health. Mega doses of vitamin D have also been shown to decrease the length of time critical care patients must remain hospitalised.24 Those who received 250,000 IUs for five days were released after an average of 25 days, compared to the average of 36 days for those receiving a placebo.

    Patients who received 500,000 IUs of vitamin D for five days were released after an average of just 18 days, effectively cutting their hospital stay in half. The health care savings in this instance alone are tremendous. When you add in all possible diseases and ailments vitamin D can prevent and/or ameliorate, the savings could potentially tally into the trillions each year.

    Certainly, for the average person, optimising your vitamin D level is one of the least expensive preventive care strategies at your disposal. If you suffer from any of the following ailments and still haven’t checked your vitamin D level, now may be the time to go ahead and do so, as research 25 into vitamin D has found it can help prevent and/or address:

    Osteoporosis, osteomalacia (bone softening) and hip fractures Type 1 and type 2 diabetes
    Cancer, including cancers of the breast, colon, prostate, ovaries, oesophagus and lymphatic system. Adding vitamin D to the conventional treatment for pancreatic cancer may also boost the effectiveness of the treatment 26 Hypertension (high blood pressure), cardiovascular disease and heart attacks – (According to vitamin D researcher Dr. Michael Holick, deficiency can raise your risk of heart attack by 50%. What’s worse, if you have a heart attack while vitamin D deficient, your risk of dying is nearly guaranteed)
    Obstructive sleep apnoea – In one study, 98% of patients with sleep apnoea had vitamin D deficiency, and the more severe the sleep apnoea, the more severe the deficiency27 Multiple sclerosis28 (“MS”) – Research shows MS patients with higher levels of vitamin D tend to experience fewer disabling symptoms
    Rheumatoid arthritis Reduced immune function
    Autoimmune diseases, including psoriasis Infections, including influenza
    Depression, 29 Seasonal Affective Disorder and psychiatric conditions such as schizophrenia Neurological disorders, including autism, dementia and Alzheimer’s 30
    Health Benefits of Sun Exposure Beyond Vitamin D

    There’s overwhelming evidence to suggest the human body evolved to obtain health benefits from, and to thrive in, sunlight. As previously noted in The Daily Mail:31

    Even taking the skin cancer risk fully into account, [scientists] say that getting a good dose of sunshine is statistically going to make us live longer, healthier and happier lives.

    One significant mechanism by which sunlight helps optimise your health is by triggering the release of nitric oxide (“NO”) when sunlight strikes your skin. 32 NO is a powerful blood pressure-lowering compound that helps protect your cardiovascular system, cutting your risk for both heart attacks and stroke.

    According to one 2013 study, 33 for every single skin cancer death, 60 to 100 people die from stroke or heart disease related to hypertension. So, your risk of dying from heart disease or stroke is on average 80 times greater than your risk of dying from skin cancer.

    Importantly, while higher vitamin D levels correlate with lower rates of cardiovascular disease, oral vitamin D supplements do not appear to benefit blood pressure, and the fact that supplements do not increase NO may be the reason for this. According to researcher Dr. Richard Weller:

    We suspect that the benefits to heart health of sunlight will outweigh the risk of skin cancer. The work we have done provides a mechanism that might account for this, and also explains why dietary vitamin D supplements alone will not be able to compensate for lack of sunlight.

    To get a thorough understanding of how UV light affects your cardiovascular function, read Weller’s paper, ‘Sunlight Has Cardiovascular Benefits Independently of Vitamin D’. 34 Research also shows that UV light:

    Helps treat and prevent the spread of diseases like tuberculosis. 35
    Helps anchor your circadian rhythm, helping you sleep better.
    Helps kill and prevent the spread of antibiotic-resistant bacteria. UV light at 254 nanometres acts as a potent bactericidal, killing drug-resistant strains of S. aureus and E. faecalis in as little as 5 seconds. 36
    Reduces your risk of myopia (short-sightedness). As reported by The Daily Mail: 37 “[R]esearchers believe that the neurotransmitter dopamine is responsible. It is known to inhibit the excessive eyeball growth that causes myopia. Sunshine causes the retina to release more dopamine.”
    Helps treat seasonal affective disorder and major depression. 38 Schizophrenia has also been linked to maternal lack of Sun exposure during pregnancy. 39
    Boosts men’s libido by increasing testosterone. Research reveals men’s testosterone levels rise and fall with the seasons. Researchers have also linked low vitamin D with an increased risk for erectile dysfunction. 40
    Helps maintain vitamin D status in elderly people at a lower cost than that of using oral vitamin D supplementation. 41 Not only could UV lamps help improve nursing home patients’ physical health, but they could also help relieve symptoms of depression.
    Lowers all-cause mortality. In one study,42,43 women who avoided Sun exposure had double the all-cause mortality rate of those who got regular Sun exposure. Another 54-month-long study, 44 involving more than 422,800 healthy adults, found that those who were most deficient in vitamin D had an 88% increased mortality risk.
    Embrace Sensible Sun Exposure as a Health-Promoting Habit

    Safe exposure to sunshine is possible by understanding your skin type, the UV strength at the time of exposure, and your duration of exposure. My advice has been clear: Always avoid sunburn. Once your skin develops the slightest tint of pink, cover up with clothing to avoid further exposure.

    The most important part of the equation is to pay close attention to your vitamin D level. Ideally, get your vitamin D tested during the peak of summer and at the end of winter to help guide your UV exposure and vitamin D supplementation. The evidence is overwhelming: You really do need sensible Sun exposure for optimal health.

    Since few foods contain any significant amount of vitamin D, and your body certainly was not designed to get its vitamin D from supplements, which are a modern invention, the only rational conclusion is that Sun exposure is the ideal way to raise your vitamin D level.

    Research has shown just how beautifully your body has been designed to use the Sun’s UV rays to promote health. It even has built-in “fail-safes” and self-regulatory processes to ensure you cannot produce too much vitamin D from Sun exposure. Plus, the vitamin D produced by UVB rays actually helps counteract the skin damage caused by UVA. It’s an intricate dance that simply cannot be fully duplicated with a supplement.

    Sources and References

    1 Ther Adv Musculoskelet Dis v.8(4); 2016 Aug
    2 Nutrients 2014; 6(10): 4472-4475
    3 ipetitions.com
    4 Anticancer Research 2011 Feb;31(2):607-11
    5 JAMA 2017;317(12):1234-1243
    6 Lab Manager March 30, 2017
    7 Newswise March 28, 2017
    8 Time March 28, 2017
    9 PLOS ONE 2016; 11 (4): e0152441
    10 PR Web April 6, 2016
    11 UC San Diego Health April 6, 2016
    12 Science World Report April 13, 2016
    13 Oncology Nurse Advisor April 22, 2016
    14 Tech Times April 11, 2016
    15 Chrisbeatcancer.com, Vitamin D
    16 Cancer Prev Res (Phila). 2015 Aug;8(8):675-82
    17 European Journal of Cancer 2005 May;41(8):1164-9
    18 Institute of Medicine, Committee to Review Dietary Reference Intakes for Vitamin D and Calcium, Dietary Reference Intakes for Calcium and Vitamin D
    19, 44 J Clin Endocrinol Metab 2013;98:2160-2167
    20 Anticancer Research February 2011: 31(2); 607-611
    21 UC San Diego Health System Press Release March 6, 2014
    22 Cancer Therapy Advisor March 23, 2016
    23 New York Times November 24, 2014
    24 Medical Press May 27, 2015
    25 Harvard T.H. Chan. Vitamin D
    26 Salk. FAQ on Pancreatic Cancer and Vitamin D
    27 Bel Marra Health May 3, 2016
    28 Mayo Clinic. Vitamin D and MS: Is There Any Connection?
    29 J Nutr Health Aging 1999;3(1): 5-7
    30 Int J Mol Sci. 2022 Dec 21;24(1):87. Vitamin D in Neurological Diseases
    31, 37 Daily Mail May 2, 2016
    32 Medical News Today May 8, 2013
    33 BBC News May 7, 2013
    34 Sunlight Institute January 18, 2016
    35 Science Daily March 17, 2009
    36 Ostomy Wound Management 1998 Oct;44(10):50-6
    38 Journal of Clinical Psychiatry 1991 May; 52(5): 213-6
    39 BBC News July 20, 2001
    40 New Hope Network May 2, 2016
    41 Photodermatol Photoimmunol Photomed 2001 Aug;17(4):168-71
    42 Journal of Internal Medicine 2014 Jul;276(1):77-86
    43 Business Insider May 7, 2014
    About the Author

    Dr. Joseph Mercola is the founder and owner of Mercola.com, a Board-Certified Family Medicine Osteopathic Physician, a Fellow of the American College of Nutrition and a New York Times bestselling author. He publishes multiple articles a day covering a wide range of topics on his website Mercola.com.




    Why do you think the satanic oligarchs, who want us sick, weak and gone, are blocking our sun from healing us?

    Health benefits of the Sun: Vitamin D can reduce the risk of cancer by as much as 67%

    Vitamin D is involved in the biology of all cells in your body, including your immune cells. A large number of studies have shown raising your vitamin D level can significantly reduce your risk of cancer...

    https://expose-news.com/2023/12/28/health-benefits-of-the-sun

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    Health benefits of the Sun: Vitamin D can reduce the risk of cancer by as much as 67% Rhoda WilsonDecember 28, 2023 Vitamin D is involved in the biology of all cells in your body, including your immune cells. A large number of studies have shown raising your vitamin D level can significantly reduce your risk of cancer. Most recently, researchers found vitamin D and calcium supplementation lowered participants’ overall cancer risk by 30%. Having a serum vitamin D level of at least 40 ng/ml reduces your risk for cancer by 67% compared to having a level of 20 ng/ml or less; most cancers occur in people with a vitamin D level between 10 and 40 ng/ml. Higher Vitamin D Levels Lower Cancer Risk By Dr. Joseph Mercola This article was originally published on 10 April 2017. Thousands of studies have been done on the health effects of vitamin D, and research shows it is involved in the biology of all cells and tissues in your body, including your immune cells. Your cells actually need the active form of vitamin D to gain access to the genetic blueprints stored inside. This is one of the reasons why vitamin D has the ability to impact such a wide variety of health problems – from foetal development to cancer. Unfortunately, despite being easy and inexpensive to address, vitamin D deficiency is an epidemic around the world. It’s been estimated that as many as 90% of pregnant mothers and newborns in the sunny Mediterranean region are even deficient in vitamin D,1 thanks to chronic Sun avoidance. A simple mathematical error may also deter many Americans and Canadians from optimising their vitamin D. The Institute of Medicine (“IOM”) recommends a mere 600 IUs of vitamin D per day for adults. As pointed out in a 2014 paper,2 the IOM underestimates the need by a factor of 10 due to a mathematical error, which has never been corrected. Grassroots Health has created a petition for the IOM and Health Canada to re-evaluate its vitamin D guidelines and correct this mathematical error.3 You can help further this important cause by signing the petition on ipetitions.com. More recent research 4 suggests it would require 9,600 IUs of vitamin D per day to get a majority (97.5%) of the population to reach 40 nanograms per millilitre (ng/ml). The American Medical Association uses of 20 ng/ml as sufficient, but research shows 40 ng/mL should be the cutoff point for sufficiency in order to prevent a wide range of diseases, including cancer. Research Again Concludes Vitamin D Lowers Cancer Risk A large number of studies have shown raising your vitamin D level can significantly reduce your risk of cancer. Most recently, a randomised clinical trial 5 by researchers at Creighton University, funded by the National Institutes of Health (“NIH”), found vitamin D and calcium supplementation lowered participants’ overall cancer risk by 30%.6,7,8 The study, which included more than 2,300 postmenopausal women from Nebraska who were followed for four years, looked at the effects of vitamin D supplementation on all types of cancer. Participants were randomly assigned to receive either 2,000 IUs of vitamin D3 in combination with 1,500 mg of calcium, or a placebo for the duration of the study. Blood testing revealed that 25-hydroxyvitamin D (25(OH)D) levels were significantly lower in those who did develop cancer. Joan Lappe, Ph.D., professor of nursing and associate dean of research at Creighton University’s College of Nursing, and lead author of the study, said: The study provides evidence that higher concentrations of 25(OH)D in the blood, in the context of vitamin D3 and calcium supplementation, decrease risk of cancer … While people can make their own vitamin D3 when they are in the Sun near mid-day, sunscreen blocks most vitamin D production. Also, due to more time spent indoors, many individuals lack adequate levels of vitamin D compounds in their blood. The results of this study lend credence to a call for more attention to the importance of vitamin D in human health and specifically in preventing cancer. Vitamin D Status Is Strongly Correlated with Cancer Risk Previous research has shown that once you reach a serum vitamin D level of 40 ng/ml, your risk for cancer diminishes by 67%, compared to having a level of 20 ng/ml or less.9,10,11,12,13,14,15 Most cancers, they found, occurred in people with a vitamin D blood level between 10 and 40 ng/ml. The optimal level for cancer protection was identified as being between 40 and 60 ng/ml. Another study 16 published in 2015 found women with vitamin D concentrations of at least 30 ng/ml had a 55% lower risk of colorectal cancer than those who had a blood level below 18 ng/ml. Even earlier research, 17 published in 2005, showed women with vitamin D levels above 60 ng/ml had an 83% lower risk of breast cancer than those with levels below 20 ng/ml! The Health and Medicine Division of the National Academies of Sciences, Engineering and Medicine (formerly IOM) has also reported an association between vitamin D and overall mortality risk from all causes, including cancer.18,19 Vitamin D also increases your chances of surviving cancer if you do get it,20,21 and this includes melanoma. 22 Access Sun Exposure as Much as Possible and Get Your Vitamin D Level Checked The UVB in sunlight is what triggers your body to produce vitamin D. I firmly believe getting regular, sensible Sun exposure is the ideal way to not only optimise your vitamin D level but maximise your health as well because sunlight also has many other important health functions. I’ll review some of these in another section below. Regular Sun exposure provides over 1,500 different wavelengths, and we’re just now rediscovering the value of many of these other wavelengths besides UVA and UVB. For example, we now know that red and infrared light helps your body form structured water, which is important for cellular function. Many do not appreciate that red, near, mid and far-infrared have many important biological functions. One of them is to improve mitochondrial function, especially the 660 nm and 830 nm wavelengths, as cytochrome C oxidase in mitochondria uses these wavelengths to produce ATP more efficiently. Vitamin D3 supplements are a poor second resort, but if you’re unable to get sufficient Sun exposure, then it’s better than nothing. As demonstrated in the featured study – which specifically looked at the effects of supplementation – they do have some benefits. Also, while not addressed in this study, I strongly recommend taking your vitamin D3 with vitamin K2 and magnesium as well, since all three work in tandem. A primary consideration when it comes to vitamin D is to get your level checked, ideally twice a year, in the middle of the summer and winter, when your level is at its highest and lowest. What you’re aiming for is a level between 40 and 60 ng/ml year-round. Grassroots Health offers vitamin D testing at a great value through its D*Action study. Read more: Harness the Power of the Sun for Health (Infographic) How to Minimise Your Risk of Skin Cancer from Sun Exposure Many avoid Sun exposure for fear of melanoma, an aggressive and potentially lethal form of skin cancer. However, it’s important to realise that melanoma occurs among those with minimal Sun exposure as well. An important risk factor for melanoma is overexposure to UV radiation. Baking in the Sun for hours on end on a weekend here and there is not a wise choice. To minimise your skin cancer risk, you want to avoid sunburn at all costs. If you’re going to the beach, bring long-sleeved cover-ups and a wide-brimmed hat, and cover up as soon as your skin starts to turn pink. Following are some general guidelines for sensible Sun exposure. If you pay close attention to these, you can determine, within reason, safe exposure durations. Know your skin type based on the Fitzpatrick skin type classification system. The lighter your skin, the less exposure to UV light is necessary. The downside is that lighter skin is also the most vulnerable to damage from overexposure. For very fair-skinned people and those with photodermatitis, any Sun exposure may be unwanted and they should carefully measure vitamin D levels while ensuring they have an adequate intake of vitamin D, vitamin K2, magnesium and calcium. For most people, safe UV exposure is possible by knowing your skin type and the current strength of the Sun’s rays. There are several apps and devices to help you optimise the benefits of Sun exposure while mitigating the risks. Also, be extremely careful if you have not been in the Sun for some time. Your first exposures of the year are the most sensitive, so be especially careful to limit your initial time in the Sun. Vitamin D Influences Your Health in Many Ways The benefits of vitamin D are not restricted to cancer prevention. In fact, the list of health benefits of vitamin D is exceedingly long. As noted earlier, researchers have now realised that vitamin D affects virtually every cell and tissue in your body, so it might be easier to list what it will not affect, rather than what it will impact. Compelling evidence suggests that optimising your vitamin D can reduce your risk of death from any cause, 23 making it a foundational component of optimal health. Mega doses of vitamin D have also been shown to decrease the length of time critical care patients must remain hospitalised.24 Those who received 250,000 IUs for five days were released after an average of 25 days, compared to the average of 36 days for those receiving a placebo. Patients who received 500,000 IUs of vitamin D for five days were released after an average of just 18 days, effectively cutting their hospital stay in half. The health care savings in this instance alone are tremendous. When you add in all possible diseases and ailments vitamin D can prevent and/or ameliorate, the savings could potentially tally into the trillions each year. Certainly, for the average person, optimising your vitamin D level is one of the least expensive preventive care strategies at your disposal. If you suffer from any of the following ailments and still haven’t checked your vitamin D level, now may be the time to go ahead and do so, as research 25 into vitamin D has found it can help prevent and/or address: Osteoporosis, osteomalacia (bone softening) and hip fractures Type 1 and type 2 diabetes Cancer, including cancers of the breast, colon, prostate, ovaries, oesophagus and lymphatic system. Adding vitamin D to the conventional treatment for pancreatic cancer may also boost the effectiveness of the treatment 26 Hypertension (high blood pressure), cardiovascular disease and heart attacks – (According to vitamin D researcher Dr. Michael Holick, deficiency can raise your risk of heart attack by 50%. What’s worse, if you have a heart attack while vitamin D deficient, your risk of dying is nearly guaranteed) Obstructive sleep apnoea – In one study, 98% of patients with sleep apnoea had vitamin D deficiency, and the more severe the sleep apnoea, the more severe the deficiency27 Multiple sclerosis28 (“MS”) – Research shows MS patients with higher levels of vitamin D tend to experience fewer disabling symptoms Rheumatoid arthritis Reduced immune function Autoimmune diseases, including psoriasis Infections, including influenza Depression, 29 Seasonal Affective Disorder and psychiatric conditions such as schizophrenia Neurological disorders, including autism, dementia and Alzheimer’s 30 Health Benefits of Sun Exposure Beyond Vitamin D There’s overwhelming evidence to suggest the human body evolved to obtain health benefits from, and to thrive in, sunlight. As previously noted in The Daily Mail:31 Even taking the skin cancer risk fully into account, [scientists] say that getting a good dose of sunshine is statistically going to make us live longer, healthier and happier lives. One significant mechanism by which sunlight helps optimise your health is by triggering the release of nitric oxide (“NO”) when sunlight strikes your skin. 32 NO is a powerful blood pressure-lowering compound that helps protect your cardiovascular system, cutting your risk for both heart attacks and stroke. According to one 2013 study, 33 for every single skin cancer death, 60 to 100 people die from stroke or heart disease related to hypertension. So, your risk of dying from heart disease or stroke is on average 80 times greater than your risk of dying from skin cancer. Importantly, while higher vitamin D levels correlate with lower rates of cardiovascular disease, oral vitamin D supplements do not appear to benefit blood pressure, and the fact that supplements do not increase NO may be the reason for this. According to researcher Dr. Richard Weller: We suspect that the benefits to heart health of sunlight will outweigh the risk of skin cancer. The work we have done provides a mechanism that might account for this, and also explains why dietary vitamin D supplements alone will not be able to compensate for lack of sunlight. To get a thorough understanding of how UV light affects your cardiovascular function, read Weller’s paper, ‘Sunlight Has Cardiovascular Benefits Independently of Vitamin D’. 34 Research also shows that UV light: Helps treat and prevent the spread of diseases like tuberculosis. 35 Helps anchor your circadian rhythm, helping you sleep better. Helps kill and prevent the spread of antibiotic-resistant bacteria. UV light at 254 nanometres acts as a potent bactericidal, killing drug-resistant strains of S. aureus and E. faecalis in as little as 5 seconds. 36 Reduces your risk of myopia (short-sightedness). As reported by The Daily Mail: 37 “[R]esearchers believe that the neurotransmitter dopamine is responsible. It is known to inhibit the excessive eyeball growth that causes myopia. Sunshine causes the retina to release more dopamine.” Helps treat seasonal affective disorder and major depression. 38 Schizophrenia has also been linked to maternal lack of Sun exposure during pregnancy. 39 Boosts men’s libido by increasing testosterone. Research reveals men’s testosterone levels rise and fall with the seasons. Researchers have also linked low vitamin D with an increased risk for erectile dysfunction. 40 Helps maintain vitamin D status in elderly people at a lower cost than that of using oral vitamin D supplementation. 41 Not only could UV lamps help improve nursing home patients’ physical health, but they could also help relieve symptoms of depression. Lowers all-cause mortality. In one study,42,43 women who avoided Sun exposure had double the all-cause mortality rate of those who got regular Sun exposure. Another 54-month-long study, 44 involving more than 422,800 healthy adults, found that those who were most deficient in vitamin D had an 88% increased mortality risk. Embrace Sensible Sun Exposure as a Health-Promoting Habit Safe exposure to sunshine is possible by understanding your skin type, the UV strength at the time of exposure, and your duration of exposure. My advice has been clear: Always avoid sunburn. Once your skin develops the slightest tint of pink, cover up with clothing to avoid further exposure. The most important part of the equation is to pay close attention to your vitamin D level. Ideally, get your vitamin D tested during the peak of summer and at the end of winter to help guide your UV exposure and vitamin D supplementation. The evidence is overwhelming: You really do need sensible Sun exposure for optimal health. Since few foods contain any significant amount of vitamin D, and your body certainly was not designed to get its vitamin D from supplements, which are a modern invention, the only rational conclusion is that Sun exposure is the ideal way to raise your vitamin D level. Research has shown just how beautifully your body has been designed to use the Sun’s UV rays to promote health. It even has built-in “fail-safes” and self-regulatory processes to ensure you cannot produce too much vitamin D from Sun exposure. Plus, the vitamin D produced by UVB rays actually helps counteract the skin damage caused by UVA. It’s an intricate dance that simply cannot be fully duplicated with a supplement. Sources and References 1 Ther Adv Musculoskelet Dis v.8(4); 2016 Aug 2 Nutrients 2014; 6(10): 4472-4475 3 ipetitions.com 4 Anticancer Research 2011 Feb;31(2):607-11 5 JAMA 2017;317(12):1234-1243 6 Lab Manager March 30, 2017 7 Newswise March 28, 2017 8 Time March 28, 2017 9 PLOS ONE 2016; 11 (4): e0152441 10 PR Web April 6, 2016 11 UC San Diego Health April 6, 2016 12 Science World Report April 13, 2016 13 Oncology Nurse Advisor April 22, 2016 14 Tech Times April 11, 2016 15 Chrisbeatcancer.com, Vitamin D 16 Cancer Prev Res (Phila). 2015 Aug;8(8):675-82 17 European Journal of Cancer 2005 May;41(8):1164-9 18 Institute of Medicine, Committee to Review Dietary Reference Intakes for Vitamin D and Calcium, Dietary Reference Intakes for Calcium and Vitamin D 19, 44 J Clin Endocrinol Metab 2013;98:2160-2167 20 Anticancer Research February 2011: 31(2); 607-611 21 UC San Diego Health System Press Release March 6, 2014 22 Cancer Therapy Advisor March 23, 2016 23 New York Times November 24, 2014 24 Medical Press May 27, 2015 25 Harvard T.H. Chan. Vitamin D 26 Salk. FAQ on Pancreatic Cancer and Vitamin D 27 Bel Marra Health May 3, 2016 28 Mayo Clinic. Vitamin D and MS: Is There Any Connection? 29 J Nutr Health Aging 1999;3(1): 5-7 30 Int J Mol Sci. 2022 Dec 21;24(1):87. Vitamin D in Neurological Diseases 31, 37 Daily Mail May 2, 2016 32 Medical News Today May 8, 2013 33 BBC News May 7, 2013 34 Sunlight Institute January 18, 2016 35 Science Daily March 17, 2009 36 Ostomy Wound Management 1998 Oct;44(10):50-6 38 Journal of Clinical Psychiatry 1991 May; 52(5): 213-6 39 BBC News July 20, 2001 40 New Hope Network May 2, 2016 41 Photodermatol Photoimmunol Photomed 2001 Aug;17(4):168-71 42 Journal of Internal Medicine 2014 Jul;276(1):77-86 43 Business Insider May 7, 2014 About the Author Dr. Joseph Mercola is the founder and owner of Mercola.com, a Board-Certified Family Medicine Osteopathic Physician, a Fellow of the American College of Nutrition and a New York Times bestselling author. He publishes multiple articles a day covering a wide range of topics on his website Mercola.com. Why do you think the satanic oligarchs, who want us sick, weak and gone, are blocking our sun from healing us? Health benefits of the Sun: Vitamin D can reduce the risk of cancer by as much as 67% Vitamin D is involved in the biology of all cells in your body, including your immune cells. A large number of studies have shown raising your vitamin D level can significantly reduce your risk of cancer... https://expose-news.com/2023/12/28/health-benefits-of-the-sun T.me/AgentsOfTruth T.me/AgentsOfTruthChat
    EXPOSE-NEWS.COM
    Health benefits of the Sun: Vitamin D can reduce the risk of cancer by as much as 67%
    Vitamin D is involved in the biology of all cells in your body, including your immune cells. A large number of studies have shown raising your vitamin D level can significantly reduce your risk of …
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  • One in four who had Pfizer Covid jabs experienced unintended immune response
    mRNA vaccines were affected by the glitch but no adverse effects were created, Cambridge researchers say

    Joe Pinkstone, Science Correspondent
    6 December 2023 • 5:17pm
    More than a quarter of people injected with mRNA Covid jabs suffered an unintended immune response created by a glitch in the way the vaccine was read by the body, a study has found...


    https://www.telegraph.co.uk/news/2023/12/06/mrna-jabs-modena-pfizer-quarter-unintended-response/

    “#mRNAs are transfected into target cells, where they are translated into recombinant protein” 👈

    https://www.nature.com/articles/s41586-023-06800-3
    One in four who had Pfizer Covid jabs experienced unintended immune response mRNA vaccines were affected by the glitch but no adverse effects were created, Cambridge researchers say Joe Pinkstone, Science Correspondent 6 December 2023 • 5:17pm More than a quarter of people injected with mRNA Covid jabs suffered an unintended immune response created by a glitch in the way the vaccine was read by the body, a study has found... https://www.telegraph.co.uk/news/2023/12/06/mrna-jabs-modena-pfizer-quarter-unintended-response/ “#mRNAs are transfected into target cells, where they are translated into recombinant protein” 👈 https://www.nature.com/articles/s41586-023-06800-3
    WWW.TELEGRAPH.CO.UK
    One in four who had Pfizer Covid jabs experienced unintended immune response
    mRNA vaccines were affected by the glitch but no adverse effects were created, Cambridge researchers say
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  • The allure of Diu lies in its pristine beaches, historical forts, and a laid-back atmosphere. Choosing the best hotel in Diu ensures that your experience of this coastal haven is nothing short of extraordinary. Imagine waking up to the gentle sound of waves, with the sun painting the sky in hues of pink and orange. This hotel offers not just accommodation but an immersive coastal retreat, where every room provides a stunning view of the sea.

    https://apanahoteldiu.in/
    The allure of Diu lies in its pristine beaches, historical forts, and a laid-back atmosphere. Choosing the best hotel in Diu ensures that your experience of this coastal haven is nothing short of extraordinary. Imagine waking up to the gentle sound of waves, with the sun painting the sky in hues of pink and orange. This hotel offers not just accommodation but an immersive coastal retreat, where every room provides a stunning view of the sea. https://apanahoteldiu.in/
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  • Virology - The Damning Evidence
    The Stake In The Heart For This Pseudoscientific Profession

    dpl
    Introduction

    One never realize how big the task of writing on a subject is until you start. One thing you can be assured of is how much you learn by writing about your findings or thoughts. My stance on virology has been clarified in two previous posts as follows:

    The Gatekeepers Club.

    Virus Lie - The Result of 4 Years of Study.

    Another thing you quickly realize on this journey is how easy it is to censor someone, especially if you start hitting a nerve. I have documented some of it underneath the conclusion of the The Gatekeepers Club article. It is very important to make copies of your work, as shadow banning is one thing, but if these platforms decide to terminate your channel and all the work you have done is on it, you will obviously lose it all. We were in that same position about a year ago when Discord decided to terminate our channel. Twenty of the smartest people you would ever know had been working on it for close to two years, and it was gone overnight. Therefore, this post will serve as safekeeping for some of the best information that I have come across in the last few weeks proving that virology is pseudoscience.


    Update - 18 September 2023

    The order of the sections of this article has been rearranged to introduce the most important information first. As mentioned in my most recent article titled: Hacking at the Root of the Virus Issue it was explained that for the longest time I thought that failure to “isolate” viruses was the most important evidence to focus on. This is however not the case as explained in detail in the “Hacking at the Root of the Virus Issue” article.

    Transmission is the fundamental assumption on which virology rest. Without proof of transmission, nothing downstream matters. Even though understanding these downstream concepts will never be a waste of time one must consider that the normal man on the street will not be interested in complicated terminology and processes.

    It is of crucial importance for the no virus community to find easier ways to explain the fallacy that is virology. Seeing as no one need a laboratory to assess whether transmission is possible and because we can observe this phenomena ourselves (Inductive reasoning) this is the linchpin for virology. A twitter space where we discussed this can be viewed here (*Note: Jamie was cut off during his talk and his section was not included).

    As discussed during the twitter space, we have reviewed the available transmission studies and a summary of these studies can be seen below.

    Transmission / Infection

    One of the funniest things you will see while debating the trolls on Twitter is that they will provide studies conducted to prove the efficacy of vaccines. The people that undertake these studies assume that transmission or infection has already been proven, but nothing could be further from the truth. That is why it is important for us to list the peer-reviewed studies that disprove transmission or infection to further demonstrate that virology is a pseudoscience. The list of studies was compiled with the help of Jamie, georgie&donny, and Aldhissla (also see Aldhissla’s list on polio here).

    (*Please note that this section is open to comments at the moment and anyone that want to add notes or studies are free to leave a comment).

    The Journal of Infectious Diseases, Vol. 2, No. 2 (Mar. 1, 1905):
    - Chapman, 1801: Tried to transmit measles using the blood, tears, the mucus of the nostrils and bronchia, and the eruptive matter in the cuticle without any success.
    - Willan, 1809: Inoculated three children with vesicle fluids of measles but without success.
    - Albers, 1834: Attempted to infect four children with measles without success. He quoted Alexander Monro, Bourgois, and Spray as also having made unsuccessful inoculations with saliva, tears, and cutaneous scales.
    - Themmen, 1817: Tried to infect 5 children with measles. 0/5 children became sick.

    Charles Creighton, 1837 (A history of epidemics in Britain). "No proof of the existence of any contagious principles by which it was propagated from one individual to another."

    EH Ackernecht, writing about Anticontagionism between 1821 and 1867 - “That the anticontagionists were usually honest men and in deadly earnest is shown, among other things, by the numerous self-experiments to which they submitted themselves to prove their contentions.” also see “Famous are the plague self-experiments of Clot-Bey, the offers for plague self-experiment by Chervin, Lassis, Costa, Lapis, and Lasserre, and the cholera self-experiments of Fay, Scipio Pinel, Wayrot, and J.L. Guyon. The amazing thing is that almost all of these experiments failed to produce the disease.”

    Note on Hospitals by Florence Nightingale, 1858 - "Suffice it to say, that in the ordinary sense of the word, there is no proof, such as would be admitted in any scientific inquiry, that there is any such thing as 'contagion." also see "Just as there is no such thing as 'contagion,' there is no such thing as inevitable 'infection."

    Andreas Christian Bull, 1868 - “It does not seem apparent in this small [polio] epidemic that contagion played any role, because the disease occurred here and there in the different places of the district without the possibility of establishing any relation between the various cases or the families of the same.”

    Karl-Oskar Medin, 1887 - A Swedish pediatrician who was the first to examine a polio outbreak, concluded that it was an infectious, but not contagious, disease.

    Charles Caverly, 1894 - Investigated the first US polio epidemic: ”it is very certain that it was non-contagious.”

    Journal of American Medical Association, Volume 72, Number 3, 1919 (or additional link here):

    - Warschawsky, 1895 - Injected small pigs and rabbits with blood taken in the eruptive stage. All results were negative.
    - Belila, 1896 - Placed warm nasal mucus and saliva from measles patients on the nasal and oral mucous membrane of rabbits, guinea-pigs, cats, mice, dogs and lambs, but without any positive results.
    - Josias, 1898 - Rubbed measles secretions over the throat, nose and eyes of several young pigs, but without any effects.
    - Geissler, 1903 - Inoculated sheep, swine, goats, dogs and cats in various ways with the bodily fluids from patients with measles; including smearing, spraying, rubbing. All results were negative.
    - Pomjalowsky, 1914 - Injected measles blood into guineapigs, rabbits and small pigs. All results were negative.
    - Jurgelunas, 1914 - Inoculated blood from patients with measles into suckling pigs and rabbits, but without effect.

    Leegaard, 1899 - Was not able to prove a single case of patient-to-patient contagion in a polio outbreak in Norway. "Infantile paralysis is of an infectious, but not of a contagious nature. As a matter of fact no indisputable instance of contagion could be proved."

    Dr. Rodermund, 1901 - From his diary of SmallPox experiments. For 15 years he smeared the pus of smallpox patients on his face and used to go home with his family, play cards at the gentleman’s club and treat other patients and never got sick or saw a single other person get sick.

    Walter Reed, 1902 - “Without entering into details, I may say that, in the first place, the Commission saw, with some surprise, what had so often been noted in the literature, that patients in all stages of yellow fever could be cared for by non-immune nurses without danger of contracting the disease. The non-contagious character of yellow fever was, therefore, hardly to be questioned.”

    Landsteiner & Popper, 1909 - "Attempts to transmit the disease [polio] to the usual laboratory animals, such as rabbits, guinea pigs, or mice, failed."

    F.E. Batten, (1909) - “Against the infectivity of the disease may be urged, first, the absence of spread of infection in hospital. The cases of poliomyelitis admitted to hospital freely mixed with other cases in the ward without any isolation or disinfection, some 70 children came in contact, but no infection took place. (p. 208, last paragraph)”

    The Boston medical and surgical journal, 1909 - An inquiry a 1908 polio outbreak found the following: “A large number of children were in intimate contact with those that were sick, and of these children an insignificant minority developed the disease.” 244 children were in intimate contact with those who were afflicted with polio. Of those 244 children, an "insignificant minority" developed the disease.

    Massachusetts State board of health, 1909 - "Poliomyelitis prevailed in epidemic form in Kansas during the summer of 1909 … No method of contagion could be found, and the author does not consider the disease contagious."

    Flexner & Lewis, 1910 - Multiple unsuccessful polio transmission attempts. "Many guinea-pigs and rabbits, one horse, two calves, three goats, three pigs, three sheep, six rats, six mice, six dogs, and four cats have had active virus introduced in the brain but without causing any appreciable effect whatever. These animals have been under observation for many weeks."

    A Washinton, 1911 - “I have not seen any cases of Polio contagion. We put the patients on one side and typhoid cases on the other, and no nurse or mother was infected. If the disease was so contagious, I don't see why the nurses and mothers would not have been infected.”

    J.J. Moren, 1912 - "Monkeys suffering from polio in the same cage with healthy monkeys, do not infect others."

    P. H. Römer, 1913 - "No proofs of the contagiousness of the disease [polio] could be obtained in the great epidemic in New York in 1907, nor in the epidemic in the Steiermark (Furntratt, Potpeschnigg) nor in Pomerania (Peiper).

    H. W. Frauenthal, 1914 - "Advocates of the contagion theory were at a loss to account for the fact that spontaneous [polio] transmission among laboratory monkeys was never known to occur ... There is no proof that spontaneous transmission of acute poliomyelitis, without an inoculation wound, can take place. There is no proof that contact contagion takes place. Spontaneous development of the disease among laboratory animals is unknown."

    W.H. Frost, 1916 - "The disease [polio] develops in a such a small proportion of people known to have been intimately associated with acute cases of polio." ... "The majority of cases of poliomyelitis can not be traced to known contact, either direct or indirect, with any previous case."

    W. L. Holt, 1916 - Investigated an epidemic of polio and found that he was "surprised that I could trace hardly any cases to personal contact with others, there rarely being successive cases."

    Dr. I. D. Rawlings, 1916 - "Any one who has had much experience with poliomyelitis is struck by the infrequency, relatively, of the secondary cases among direct contacts ... there were approximately 1,500 direct contacts, and yet but one possible case occurred among them. Also among the large number of people that came from New York and other infected areas not a single case occurred.”

    H. L. Abramson, 1917 - Attempts to induce polio in a monkey by injecting the spinal fluid of 40 polio patients (rather than the ground cord) into the brain failed.

    Dold et al. 1917 (Original paper in German from Muenchener Medizinische Wochenschrift 64 ( 1917), bottom of p 143) - Injected healthy people with the nasal secretions taken from one ill person, 1/40 healthy people became ill.

    A review of the investigations concerning the etiology of measels, A. W. Sellards
    harvard Medical School. Boston, Massachusetts as seen below:
    - Jurgelunas, 1914: Tried to produce measles in monkeys using inoculations of the blood and mucus secretions from measles patients as well as by exposing the animals to patients in measles wards. All results were negative.
    - Sellards, 1918: Tried to transmit measles to 8 healthy volunteers without a prior history of measles exposure. 0/8 men became sick after multiple failed attempts.
    - Sellards and Wenworth, 1918: Inoculated 3 monkeys in various ways, including intensive injections of blood from measles patients. The animals remained well.
    - Sellards and Wenworth, 1918: Blood from measles patients was injected simultaneously into 2 men and 2 monkeys. Both men remained symptom-free. One of the two monkeys developed symptoms that were not suggestive of measles.

    Milton Rosenau, 1918 - Professor of preventive medicine and hygiene at Harvard, notes that "monkeys have so far never been known to contract the disease [polio] spontaneously, even though they are kept in intimate association with infected monkeys." Page 341.

    Hess & Unger, 1918 - "In three instances the nasal secretion of varicella patients was applied to the nostrils; in three others the tonsillar secretion to the tonsils, and in six, the tonsillar and pharyngeal secretions were transferred to the nose, the pharynx, and the tonsils. In none of these twelve cases was there any reaction whatsoever, either local or systemic."

    Hess & Unger, 1918 - The vesicle fluids from people with chickenpox was injected intravenously into 38 children. 0/38 became sick.

    Published in the Journal - American Medical Association, 1919 - Need Of Further Research On The Transmissibility Of Measles And Varicella. “Evidently in our experiments we do not, as we believe, pursue nature's mode of transmission; either we fail to carry over the virus, or the path of infection is quite different from what it is commonly thought to be.”

    Milton J. Rosenau, March 1919 - Conducted 9 separate experiments in a group of 49 healthy men, to prove contagion. In all 9 experiments, 0/49 men became sick after being exposed to sick people or the bodily fluids of sick people.

    More information on the Rosenau studies here.

    Wahl et al, 1919 - Conducted 3 separate trials on six men attempting to infect them with different strains of Influenza. Not a single person got sick.

    Schmidt et al, 1920 (Original paper in German here) - Conducted two controlled experiments, exposing healthy people to the bodily fluids of sick people. Of 196 people exposed to the mucous secretions of sick people, 21 (10.7%) developed colds and three developed grippe (1.5%). In the second group, of the 84 healthy people exposed to mucous secretions of sick people, five developed grippe (5.9%) and four colds (4.7%). Of forty-three controls who had been inoculated with sterile physiological salt solutions eight (18.6%) developed colds. A higher percentage of people got sick after being exposed to saline compared to those being exposed to the “virus”.

    Williams et al, 1921 - Tried to experimentally infect 45 healthy men with the common cold and influenza, by exposing them to mucous secretions from sick people. 0/45 became ill.

    Mahatma Gandhi, 1921 - "and the poison that accumulates in the system is expelled in the form of small-pox. If this view is correct, then there is absolutely no need to be afraid of small-pox" also see "This has given rise to the superstition that it is a contagious disease, and hence to the attempt to mislead the people into the belief that vaccination is an effective means of preventing it."

    Blanc and Caminopetros, 1922 (original paper in French here) - Material from nine cases of shingles was inoculated into the eyes, cornea, conjunctiva, skin, brain, and spinal cord of a series of animals, including rabbits, mice, sheep, pigeons, monkeys, and a dog. All results were negative.

    Robertson & Groves, 1924 - Exposed 100 healthy individuals to the bodily secretions from 16 different people suffering from influenza. 0 people of 100 whom they deliberately tried to infect with Influenza got sick That is because Viruses don't cause disease.

    Bauguess, 1924 - "A careful search of the literature does not reveal a case in which the blood from a patient having measles was injected into the blood stream of another person and produced measles."

    The problem of the etiology of herpes zoster, 1925 - "Many other authors report entirely negative results following the inoculation of herpes zoster material into the sacrified corneas of rabbits: Kraupa (18); Baum (19); LSwenstein (8), Teissier, Gastinel, and Reilly (20) ; Kooy (21) ; Netter and Urbain (22); Bloch and Terris (23); Simon and Scott (24); and Doerr (25). It is evident, therefore, that the results of attempts to inoculate animals with material from cases of herpes zoster must be considered at present to be inconclusive."

    Volney S and Chney M.D., 1928 - A study where it is clearly stated that cold is not infectious.

    Dochez et al, 1930 - Attempted to infect 11 men with intranasal influenza. Not a single person got sick. Most strikingly one person got very sick when he accidently found out that is what they were trying to do. His symptoms disappeared when they told him he was misinformed.

    L. L. Lumsden, 1935 - “Painstaking efforts were made throughout the studies to obtain all traces of transmission of the disease through personal contact, but it appears that in this outbreak in Louisville evidence of personal association between the cases of poliomyelitis, suggestive of cause and effect, was no more common than that which might have been found if histories had been taken of personal association between cases of broken bones occurring in the city in the same period.”

    Thomas Francis Jr et al, 1936 - Gave 23 people influenza via 3 different methods. 0 people got sick.. They gave 2 people already "suffering from colds" the influenza who also did not get sick

    Burnet and Lush, 1937 - 200 people given "Melbourne type" Influenza . 0 people showed any symptoms of disease. 200/0.

    Lumsden, 1938 - "It is quite usual in small [polio] outbreaks in rural counties for individual cases to develop in separate homes three or for miles apart without there being any evidence of direct or indirect personal contact having operated between persons afflicted."

    L. L Lumsden, 1938 - ”The general and usual epidemiological features of the disease [polio] all appear opposed to the hypothesis that poliomyelitis is a contagious disease spread among human beings by nose-to-nose or any other direct personal contact.”

    Burnet and Foley, 1940 - Attempted to experimentally infect 15 university students with influenza. The authors concluded their experiment was a failure.

    Thomas Francis Jr, 1940 - Gave 11 people "Epidemic Influenza" 0 people got sick. That is because viruses don't cause disease.

    John Toomey, 1941 - A veteran polio researcher: "no animal gets the disease from another, no matter how intimately exposed."

    A. R. Kendall, 1945 - “The epidemiological facts of poliomyelitis are these: … (2) A majority of cases of clinically diagnosable poliomyelitis (polioparalysis) occur sporadically, with no history of contact with previous cases. (3) Two cases of polioparalysis in one family are unusual, even though no precautions are taken to prevent cross infection. (4) Clinically diagnosable cases of poliomyelitis (polioparalysis) show little tendency to spread, even in schools or other places of public gathering. (5) Incidence of polioparalysis is no greater among doctors and nurses, in intimate contact with acute cases than it is among the civil population, even though the former are exposed freely to infection.” […] “Polioparalysis is not contagious.”

    E. B. Shaw & H. E. Thelander, 1949 - “The epidemiology of the disease [polio] remains obscure. There has been a tendency to depart from an early theory that the disease spreads by means of direct contact.”

    Albert Sabin, 1951 (inventor of the polio vaccine). "There is no evidence for the transmission of poliomyelitis by droplet nuclei."

    Archibald L. Hoyne, 1951 (alternative link here) - “However, in the Cook County Contagious Disease Hospital where the latter procedure has not been used there has never been a doctor, intern, nurse or any other member of the personnel who contracted poliomyelitis within a period of at least thirty-five years, nor has any patient ever developed poliomyelitis after admission to the hospital.”

    Ralph R. Scobey, 1951 - ”Although poliomyelitis is legally a contagious disease, which implies that it is caused by a germ or virus, every attempt has failed conclusively to prove this mandatory requirement of the public health law.” Professor of clinical pediatrics and president of the Poliomyelitis Research Institute, Syracuse, N.Y.

    Ralph R. Scobey, 1952 - "In addition to the failure to prove contagiousness of human poliomyelitis, it has likewise been impossible to prove contagiousness of poliomyelitis in experimental animals."

    Douglas Gordon et al, 1975 - This study gave 10 people English type Influenza and 10 people a placebo. The study was negative. Most telling is they admit that mild symptoms were seen in the placebo group, proving that the inoculation methods cause them.

    Beare et al 1980 (refer to reference 6 in the linked paper). Quote from John J Cannell, 2008 as follows - “An eighth conundrum – one not addressed by Hope-Simpson – is the surprising percentage of seronegative volunteers who either escape infection or develop only minor illness after being experimentally inoculated with a novel influenza virus.”

    Nancy Padian, 1996 - A study which followed 176 discordant couples (1 HIV positive and the other negative) for 10 years. These couples regularly slept together and had unprotected sex. There were no HIV transmissions from the positive partner to the negative partner during the entirety of the study.

    John Treanor et al, 1999 - Gave 108 people Influenza A. Only 35% recorded mild symptoms such as stuffy nose. Unfortunately 35% of the placebo control group also developed mild symptoms proving the methods of inoculation are causing them.

    Bridges et al, 2003 - "Our review found no human experimental studies published in the English-language literature delineating person-to-person transmission of influenza... Thus, most information on human-to-human transmission of influenza comes from studies of human inoculation with influenza virus and observational studies."

    The Virology Journal, 2008 - ”There were five attempts to demonstrate sick-to-well influenza transmission in the desperate days following the pandemic [1918 flu] and all were ’singularly fruitless’ … all five studies failed to support sick-to-well transmission, in spite of having numerous acutely ill influenza patients, in various stages of their illness, carefully cough, spit, and breathe on a combined total of >150 well patients.”

    Public Health Reports, 2010 - ”It seemed that what was acknowledged to be one of the most contagious of communicable diseases [1918 flu] could not be transferred under experimental conditions.”

    Jasmin S Kutter, 2018, - Our observations underscore the urgent need for new knowledge on respiratory virus transmission routes and the implementation of this knowledge in infection control guidelines to advance intervention strategies for currently circulating and newly emerging viruses and to improve public health.
    - There is a substantial lack of (experimental) evidence on the transmission routes of PIV (types 1–4) and HMPV.
    - Extensive human rhinovirus transmission experiments have not led to a widely accepted view on the transmission route [35, 36, 37, 38, 39, 40].
    - However, until today, results on the relative importance of droplet and aerosol transmission of influenza viruses stay inconclusive and hence, there are many reviews intensively discussing this issue [10, 45, 46, 47, 48, 49, 50].
    - Despite this, the relative importance of transmission routes of respiratory viruses is still unclear, depending on the heterogeneity of many factors like the environment (e.g. temperature and humidity), pathogen and host [5, 19].

    Jonathan Van Tam, 2020 - Conducted these human trials of Flu A in 2013. 52 people were intentionally given "Flu A" and made to live in controlled conditions with 75 people. 0 people sick. 0 PCR positive.

    J.S. Kutter, 2021 - “Besides nasal discharge, no other signs of illness were observed in the A/H1N1 virus-positive donor and indirect recipient animals.” The animals were subsequently euthanized after the animals experienced what the scientist describe as having breathing difficulties (no further details were given to describe their condition). *Refer to Note 1.

    Ben Killingley, 2022 - Gave 36 people what he considered to be purified Covid Virus Intranasally. The Results: Nobody got sick. *Refer to Note 2.

    Notes

    *Note 1 - Jasmin Kutter, 2021:

    From the Results section: “Throat and nasal swabs were collected from the donor and indirect recipient animals on alternating days.” This on its own can lead to nasal discharge which is the only “sign of illness” that was noted in this study.

    *Note 2 - Ben Killingley, 2022:

    See the video explanation by Jamie here.

    Ben Killingley also conducted a study in the early 2010's in which he had inoculated people in a room with 75 others some wearing masks others as a control. Not a single person even tested PCR positive. Some links to his previous studies include a 2011, 2019 and a 2020 study.

    It is assumed that his latest, 2022 study, is a follow up to cover the findings of his previous findings. Some additional notes on the study referenced include:

    - They gave 10 people the potent nephrotoxin Remdisivir.

    - They measure sickness by means of a PCR test which isn't indicative of disease because it can tests positive with “asymptomatic” cases as well.

    - Even if you say that a runny nose after swabbing is Covid. A 50% outcome to a direct challenge of something is a negative result. It doesn't suggest causation which would need to be at least 90%.

    - The very methods of inoculation used during the study could cause the nasal congestion/discharge (which is their measure of whether someone is sick or not). This has been shown in previous studies.

    - Lastly nobody was given "regeneron" because nobody got "sick".

    *Note 3 - Dr Robert Willner, 1994:

    December 7th 1994 Hollywood Roosevelt Hotel, Greensboro, N.C., Dr Willner (a medical doctor of 40 years experience) an outspoken whistleblower of the AIDS hoax. In front of a gathering of about 30 alternative-medicine practitioners and several journalists, Willner stuck a needle in the finger of Andres, 27, a Fort Lauderdale student who says he has tested positive for HIV. Then, wincing, the 65-year-old doctor stuck himself. In 1993, Dr. Willner stunned Spain by inoculating himself with the blood of Pedro Tocino, an HIV positive hemophiliac. This demonstration of devotion to the truth and the Hippocratic Oath he took, nearly 40 years before, was reported on the front page of every major newspaper in Spain. His appearance on Spain’s most popular television show envoked a 4 to 1 response by the viewing audience in favor of his position against the “AIDS hypothesis.” When asked why he would put his life on the line to make a point, Dr. Willner replied: “I do this to put a stop to the greatest murderous fraud in medical history. By injecting myself with HIV positive blood, I am proving the point as Dr. Walter Reed did to prove the truth about yellow fever. In this way it is my hope to expose the truth about HIV in the interest of all mankind.” He tested negative multiple times. He died of a Heart attack 4 months later 15th April 1995 (yeh right, funny how these naysayers all die suddenly. Link to the presentation here.

    Ludicrous “Transmission” Studies

    The picture of virology’s ludicrousy won’t be complete without a list of studies showing the insanity of what virologists claim to be transmission of disease. This include the injection of fluids into the brains and lungs of animals and we may just include some epidemiological studies to show how these are also not proof of anything. Joe Hendry mostly put it together and the papers we have are as follows (*Please note that this section is open to comments at the moment and anyone that want to add notes or studies are free to leave a comment):

    Louis Pasteur, 1881 - For rabies, tried to demonstrate transmission by injecting diseased brain tissue "directly onto the surface of the brain of a healthy dog through a hole drilled into its skull."

    Simon Flexner and Paul A. Lewis, 1910 - Spinal cords from deceased children were ground up and emulsified to be injected into the brains of monkeys. Study explained in detail here.

    John F. Anderson and Joseph Goldberger, 1911 - Injected blood from a measles patient directly into the heart and brains of monkeys.

    Carl Tenbroeck, 1918 - A mixture of ground up rat's livers, spleens, kidneys,
    testicles, lungs, hearts, and brains was injected into the brains of other rats.

    Claus W. Jungeblut, 1931 - Ground up monkey spinal cord was injected into the brains of other monkeys.

    Wilson Smith, 1933 - “The infected animal is killed when showing symptoms, often at the beginning of the second temperature rise. The turbinates are scraped out, ground up with sand, and emulsified in about 20 c.cm. of equal parts of broth and saline. The emulsion is lightly centrifuged, and about 1 c.cm. of the supernatant fluid is dropped into the nostrils of another ferret.”

    Thomas Francis and Jr, T. P. Magill, 1935 - Ground up ferret lung tissue was injected into the brains of rabbits.

    Ann G. Kuttner and T'sun T'ung, 1935 - Ground up kidney and brain of a guinea pig was injected into the brain of another guinea pig.

    Erich Traub. April 01 1936 - Ground up mouse brain was injected into the brains of guinea pigs.

    Albert B. Sabin and Peter K. Olitsky, 1937 - Ground up mouse brain was injected into the brains of other mice.

    G. John Buddingh, 1938 - Ground up chick embryo was injected into the brains 2 or 3 day old chicks.

    Gilbert Dalldorf, 1939 - Ground up ferret spleens was injected into the brains of mice.

    Claus W. Jungeblut et al, 1942 - Ground up brain or spinal cord of paralyzed mice was injected into the brains of 13 monkeys.

    Henry Pinkerton and Vicente Moragues, 1942 - Ground up brain tissue from dying mice was injected into the brains of pigeons.

    C. Kling et al, 1942 - Injected sewage sludge into the brains and abdomen of monkeys. This convinced him that he had isolated a virus and proven that the sewer is a vehicle for polio transmission.

    D.M. Horstmann, 1944 - Allegedly "proved" that the feces of polio patients contained "poliovirus" by injecting fecal samples into monkeys' brains and spines.

    Joseph E. Smadel et al, 1945 - Ground up pigeon spleen was injected into the brains of mice.

    F. Sargent Cheever et al, 1949 - Ground up mouse brain was injected into the brains of rats and hamsters.

    Isolation

    Isolation has been well defined in Virus Lie - The Result of 4 Years of Study and to this day there has not been a single paper presented that could show the isolation of a virus without first contaminating the sample. This is shown in detail in the virus lie article and will not be repeated here again. One interesting point that can be captured here is all the studies showing a control test proving that the isolation method used for viruses is flawed. They can be listed as follows:

    John F Enders, 1954 - Under other agents isolated during the study. "A second agent was obtained from an uninoculated culture of monkey kidney cells. The cytopathic changes it induced in the unstained preparations could not be distinguished with confidence from the viruses isolated from measles." It is highlighted here. Refer to the video explanation here.

    Image
    It is further discussed in the paper that "While there is no ground for concluding that the factors in vivo (in the body) are the same as those which underlie the formation of giant cells and the nuclear disturbances in vitro (outside a living organism), the appearance of these phenomena in cultured cells is consistent with the properties that a priori might be associated with the virus of measles.”

    Image
    Rustigian et al, 1955 - This paper is described in an article by Viroliegy here (look under Rustigain in the article).

    Cohen et al, 1955 - This paper is also described in the same article by Viroliegy here (look under Cohen in the article).

    Bech and von Magnus, 1959 - This paper is also described in the same article by Viroliegy here (look under Von Magnus in the article).

    F Rapp et al, 1959 - This paper is described in a video by Spacebusters here. Most noteworthy is “Monkey kidney cells, however, are unsuitable for the investigations of the type reported here; Peebles et al. and Ruckle showed that monkeys, and cell cultures derived from them, are often infected with an agent serologically indistinguishable from human measles virus, which causes cytopathic changes in monkey kidney cell cultures almost identical with those caused by human measles virus.”

    Image
    Carl J. O’Hara et al, 1988 - The study demonstrated "HIV" particles in 18 out of 20 (90% of) AIDS-related lymph node enlargements but also in 13 out of 15 (88% of) non-AIDS-related enlargements. Which means that particles claimed to be HIV virions are non-specific since identical particles can be found in the majority of patients with enlarged lymph nodes not attributed to AIDS, and at no risk for developing AIDS. Refer to @Aldhissla45’s tweet here.

    P Gluschankof et al, 1997 - This paper described in a video here with additional notes by Jamie here.

    Julian W. Bess Jr., 1997 - This paper described in a video here with additional notes by Jamie here.

    C.A. Cassol, 2020 - This paper is described by Andrew Kaufman here as well as by Thomas Cowan here.

    “Unofficially” we can also add the Lanka 3 phase control experiment that can be seen here or searched for it here.

    A further indication of the isolation procedure fallacy is shown in a study during which the CPE becomes more well defined with the addition of specific substances. The study is as follows:

    Leon Caly et al, 2020 - “Following several failures to recover virions with the characteristic fringes of surface spike proteins, it was found that adding trypsin to the cell culture medium immediately improved virion morphology.” See a video explanation here.

    Recent Requests and Statements

    Further and more recent requests and statements that were sent to me by my good friend Courtenay are as follows:

    May 5, 2022:
    U.S. CDC and Agency for Toxic Substances and Disease Registry confirmed that a search of their records failed to find any that describe anyone on Earth finding an alleged “avian influenza virus” in the bodily fluids of any diseased diseased host (animal or human) and purifying “it”… which is necessary so that “it” could be sequenced, characterized and studied with controlled experiments. This can be viewed here.

    May 20, 2022:
    Public Health Agency of Canada confirmed that they have no record of any alleged “avian influenza virus” having been found and purified from the bodily fluid/tissue/excrement of any diseased “host” on the planet (in order for “it” to be sequenced, characterized and studied with controlled experiments) by anyone, anywhere, ever.
    Insanely, they insist that:

    “Viruses” are in hosts despite their utter inability to find them there,.

    It’s necessary to “grow them” in non-host cells (as if “they” would grow better there than they allegedly grew in the diseased host lol).

    They pretend that mixing complex substances together results in purification.

    This can be viewed here.

    December 20, 2021:
    Public Health Agency of Canada confirmed that they have no record of any alleged “virus” having been purified from a sample taken from any diseased human on Earth, by anyone, ever, period. To be viewed here.

    March 11, 2022:
    U.S. Centers for Disease Control and Prevention and Agency for Toxic Substances and Disease Registry respond to a FOIA request for all studies / reports in their possession, custody or control describing the purification of any “virus” addressed by any “vaccine” on either their childhood or adult U.S. “immunization” schedule, directly from a sample taken from any diseased "host" on Earth where the sample was not first combined with any other source of genetic material. CDC/ATSDR provided 5 studies on “rotavirus” (thereby admitting they have no records for any other alleged viruses). None of these 5 studies actually describe isolation/purification of a “rotavirus” from a human.
    Request, response, studies to be viewed here.

    March 8, 2023:
    Italy 2020: Inside Covid’s “Ground zero” in Europe - Three years ago the Western World came to a standstill. The official Covid-19 narrative depicted a strange suddenly-super-spreading, deadlier-than-flu virus hailing from China that landed in Northern Italy.

    On February 20, 2020 the first alleged case of Covid-19 was discovered in the West in the Lombardy town of Codogno, Italy. Later that day the Italian government reported their first “Covid-19 death.”

    Dramatic media reports emerging from Northern Italy were hammered into and onto the Western psyche giving the impression there was a mysterious “super spreading” and “super lethal” novel virus galloping across the region infecting and killing scores of people.

    Read the rest of the report here.

    Conclusion

    The above list will be worked on over the coming years. If you think that any corrections need to be made or if you want to add additional studies, please leave a comment.


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    https://open.substack.com/pub/dpl003/p/virology-the-damning-evidence?r=29hg4d&utm_medium=ios&utm_campaign=post
    Virology - The Damning Evidence The Stake In The Heart For This Pseudoscientific Profession dpl Introduction One never realize how big the task of writing on a subject is until you start. One thing you can be assured of is how much you learn by writing about your findings or thoughts. My stance on virology has been clarified in two previous posts as follows: The Gatekeepers Club. Virus Lie - The Result of 4 Years of Study. Another thing you quickly realize on this journey is how easy it is to censor someone, especially if you start hitting a nerve. I have documented some of it underneath the conclusion of the The Gatekeepers Club article. It is very important to make copies of your work, as shadow banning is one thing, but if these platforms decide to terminate your channel and all the work you have done is on it, you will obviously lose it all. We were in that same position about a year ago when Discord decided to terminate our channel. Twenty of the smartest people you would ever know had been working on it for close to two years, and it was gone overnight. Therefore, this post will serve as safekeeping for some of the best information that I have come across in the last few weeks proving that virology is pseudoscience. Update - 18 September 2023 The order of the sections of this article has been rearranged to introduce the most important information first. As mentioned in my most recent article titled: Hacking at the Root of the Virus Issue it was explained that for the longest time I thought that failure to “isolate” viruses was the most important evidence to focus on. This is however not the case as explained in detail in the “Hacking at the Root of the Virus Issue” article. Transmission is the fundamental assumption on which virology rest. Without proof of transmission, nothing downstream matters. Even though understanding these downstream concepts will never be a waste of time one must consider that the normal man on the street will not be interested in complicated terminology and processes. It is of crucial importance for the no virus community to find easier ways to explain the fallacy that is virology. Seeing as no one need a laboratory to assess whether transmission is possible and because we can observe this phenomena ourselves (Inductive reasoning) this is the linchpin for virology. A twitter space where we discussed this can be viewed here (*Note: Jamie was cut off during his talk and his section was not included). As discussed during the twitter space, we have reviewed the available transmission studies and a summary of these studies can be seen below. Transmission / Infection One of the funniest things you will see while debating the trolls on Twitter is that they will provide studies conducted to prove the efficacy of vaccines. The people that undertake these studies assume that transmission or infection has already been proven, but nothing could be further from the truth. That is why it is important for us to list the peer-reviewed studies that disprove transmission or infection to further demonstrate that virology is a pseudoscience. The list of studies was compiled with the help of Jamie, georgie&donny, and Aldhissla (also see Aldhissla’s list on polio here). (*Please note that this section is open to comments at the moment and anyone that want to add notes or studies are free to leave a comment). The Journal of Infectious Diseases, Vol. 2, No. 2 (Mar. 1, 1905): - Chapman, 1801: Tried to transmit measles using the blood, tears, the mucus of the nostrils and bronchia, and the eruptive matter in the cuticle without any success. - Willan, 1809: Inoculated three children with vesicle fluids of measles but without success. - Albers, 1834: Attempted to infect four children with measles without success. He quoted Alexander Monro, Bourgois, and Spray as also having made unsuccessful inoculations with saliva, tears, and cutaneous scales. - Themmen, 1817: Tried to infect 5 children with measles. 0/5 children became sick. Charles Creighton, 1837 (A history of epidemics in Britain). "No proof of the existence of any contagious principles by which it was propagated from one individual to another." EH Ackernecht, writing about Anticontagionism between 1821 and 1867 - “That the anticontagionists were usually honest men and in deadly earnest is shown, among other things, by the numerous self-experiments to which they submitted themselves to prove their contentions.” also see “Famous are the plague self-experiments of Clot-Bey, the offers for plague self-experiment by Chervin, Lassis, Costa, Lapis, and Lasserre, and the cholera self-experiments of Fay, Scipio Pinel, Wayrot, and J.L. Guyon. The amazing thing is that almost all of these experiments failed to produce the disease.” Note on Hospitals by Florence Nightingale, 1858 - "Suffice it to say, that in the ordinary sense of the word, there is no proof, such as would be admitted in any scientific inquiry, that there is any such thing as 'contagion." also see "Just as there is no such thing as 'contagion,' there is no such thing as inevitable 'infection." Andreas Christian Bull, 1868 - “It does not seem apparent in this small [polio] epidemic that contagion played any role, because the disease occurred here and there in the different places of the district without the possibility of establishing any relation between the various cases or the families of the same.” Karl-Oskar Medin, 1887 - A Swedish pediatrician who was the first to examine a polio outbreak, concluded that it was an infectious, but not contagious, disease. Charles Caverly, 1894 - Investigated the first US polio epidemic: ”it is very certain that it was non-contagious.” Journal of American Medical Association, Volume 72, Number 3, 1919 (or additional link here): - Warschawsky, 1895 - Injected small pigs and rabbits with blood taken in the eruptive stage. All results were negative. - Belila, 1896 - Placed warm nasal mucus and saliva from measles patients on the nasal and oral mucous membrane of rabbits, guinea-pigs, cats, mice, dogs and lambs, but without any positive results. - Josias, 1898 - Rubbed measles secretions over the throat, nose and eyes of several young pigs, but without any effects. - Geissler, 1903 - Inoculated sheep, swine, goats, dogs and cats in various ways with the bodily fluids from patients with measles; including smearing, spraying, rubbing. All results were negative. - Pomjalowsky, 1914 - Injected measles blood into guineapigs, rabbits and small pigs. All results were negative. - Jurgelunas, 1914 - Inoculated blood from patients with measles into suckling pigs and rabbits, but without effect. Leegaard, 1899 - Was not able to prove a single case of patient-to-patient contagion in a polio outbreak in Norway. "Infantile paralysis is of an infectious, but not of a contagious nature. As a matter of fact no indisputable instance of contagion could be proved." Dr. Rodermund, 1901 - From his diary of SmallPox experiments. For 15 years he smeared the pus of smallpox patients on his face and used to go home with his family, play cards at the gentleman’s club and treat other patients and never got sick or saw a single other person get sick. Walter Reed, 1902 - “Without entering into details, I may say that, in the first place, the Commission saw, with some surprise, what had so often been noted in the literature, that patients in all stages of yellow fever could be cared for by non-immune nurses without danger of contracting the disease. The non-contagious character of yellow fever was, therefore, hardly to be questioned.” Landsteiner & Popper, 1909 - "Attempts to transmit the disease [polio] to the usual laboratory animals, such as rabbits, guinea pigs, or mice, failed." F.E. Batten, (1909) - “Against the infectivity of the disease may be urged, first, the absence of spread of infection in hospital. The cases of poliomyelitis admitted to hospital freely mixed with other cases in the ward without any isolation or disinfection, some 70 children came in contact, but no infection took place. (p. 208, last paragraph)” The Boston medical and surgical journal, 1909 - An inquiry a 1908 polio outbreak found the following: “A large number of children were in intimate contact with those that were sick, and of these children an insignificant minority developed the disease.” 244 children were in intimate contact with those who were afflicted with polio. Of those 244 children, an "insignificant minority" developed the disease. Massachusetts State board of health, 1909 - "Poliomyelitis prevailed in epidemic form in Kansas during the summer of 1909 … No method of contagion could be found, and the author does not consider the disease contagious." Flexner & Lewis, 1910 - Multiple unsuccessful polio transmission attempts. "Many guinea-pigs and rabbits, one horse, two calves, three goats, three pigs, three sheep, six rats, six mice, six dogs, and four cats have had active virus introduced in the brain but without causing any appreciable effect whatever. These animals have been under observation for many weeks." A Washinton, 1911 - “I have not seen any cases of Polio contagion. We put the patients on one side and typhoid cases on the other, and no nurse or mother was infected. If the disease was so contagious, I don't see why the nurses and mothers would not have been infected.” J.J. Moren, 1912 - "Monkeys suffering from polio in the same cage with healthy monkeys, do not infect others." P. H. Römer, 1913 - "No proofs of the contagiousness of the disease [polio] could be obtained in the great epidemic in New York in 1907, nor in the epidemic in the Steiermark (Furntratt, Potpeschnigg) nor in Pomerania (Peiper). H. W. Frauenthal, 1914 - "Advocates of the contagion theory were at a loss to account for the fact that spontaneous [polio] transmission among laboratory monkeys was never known to occur ... There is no proof that spontaneous transmission of acute poliomyelitis, without an inoculation wound, can take place. There is no proof that contact contagion takes place. Spontaneous development of the disease among laboratory animals is unknown." W.H. Frost, 1916 - "The disease [polio] develops in a such a small proportion of people known to have been intimately associated with acute cases of polio." ... "The majority of cases of poliomyelitis can not be traced to known contact, either direct or indirect, with any previous case." W. L. Holt, 1916 - Investigated an epidemic of polio and found that he was "surprised that I could trace hardly any cases to personal contact with others, there rarely being successive cases." Dr. I. D. Rawlings, 1916 - "Any one who has had much experience with poliomyelitis is struck by the infrequency, relatively, of the secondary cases among direct contacts ... there were approximately 1,500 direct contacts, and yet but one possible case occurred among them. Also among the large number of people that came from New York and other infected areas not a single case occurred.” H. L. Abramson, 1917 - Attempts to induce polio in a monkey by injecting the spinal fluid of 40 polio patients (rather than the ground cord) into the brain failed. Dold et al. 1917 (Original paper in German from Muenchener Medizinische Wochenschrift 64 ( 1917), bottom of p 143) - Injected healthy people with the nasal secretions taken from one ill person, 1/40 healthy people became ill. A review of the investigations concerning the etiology of measels, A. W. Sellards harvard Medical School. Boston, Massachusetts as seen below: - Jurgelunas, 1914: Tried to produce measles in monkeys using inoculations of the blood and mucus secretions from measles patients as well as by exposing the animals to patients in measles wards. All results were negative. - Sellards, 1918: Tried to transmit measles to 8 healthy volunteers without a prior history of measles exposure. 0/8 men became sick after multiple failed attempts. - Sellards and Wenworth, 1918: Inoculated 3 monkeys in various ways, including intensive injections of blood from measles patients. The animals remained well. - Sellards and Wenworth, 1918: Blood from measles patients was injected simultaneously into 2 men and 2 monkeys. Both men remained symptom-free. One of the two monkeys developed symptoms that were not suggestive of measles. Milton Rosenau, 1918 - Professor of preventive medicine and hygiene at Harvard, notes that "monkeys have so far never been known to contract the disease [polio] spontaneously, even though they are kept in intimate association with infected monkeys." Page 341. Hess & Unger, 1918 - "In three instances the nasal secretion of varicella patients was applied to the nostrils; in three others the tonsillar secretion to the tonsils, and in six, the tonsillar and pharyngeal secretions were transferred to the nose, the pharynx, and the tonsils. In none of these twelve cases was there any reaction whatsoever, either local or systemic." Hess & Unger, 1918 - The vesicle fluids from people with chickenpox was injected intravenously into 38 children. 0/38 became sick. Published in the Journal - American Medical Association, 1919 - Need Of Further Research On The Transmissibility Of Measles And Varicella. “Evidently in our experiments we do not, as we believe, pursue nature's mode of transmission; either we fail to carry over the virus, or the path of infection is quite different from what it is commonly thought to be.” Milton J. Rosenau, March 1919 - Conducted 9 separate experiments in a group of 49 healthy men, to prove contagion. In all 9 experiments, 0/49 men became sick after being exposed to sick people or the bodily fluids of sick people. More information on the Rosenau studies here. Wahl et al, 1919 - Conducted 3 separate trials on six men attempting to infect them with different strains of Influenza. Not a single person got sick. Schmidt et al, 1920 (Original paper in German here) - Conducted two controlled experiments, exposing healthy people to the bodily fluids of sick people. Of 196 people exposed to the mucous secretions of sick people, 21 (10.7%) developed colds and three developed grippe (1.5%). In the second group, of the 84 healthy people exposed to mucous secretions of sick people, five developed grippe (5.9%) and four colds (4.7%). Of forty-three controls who had been inoculated with sterile physiological salt solutions eight (18.6%) developed colds. A higher percentage of people got sick after being exposed to saline compared to those being exposed to the “virus”. Williams et al, 1921 - Tried to experimentally infect 45 healthy men with the common cold and influenza, by exposing them to mucous secretions from sick people. 0/45 became ill. Mahatma Gandhi, 1921 - "and the poison that accumulates in the system is expelled in the form of small-pox. If this view is correct, then there is absolutely no need to be afraid of small-pox" also see "This has given rise to the superstition that it is a contagious disease, and hence to the attempt to mislead the people into the belief that vaccination is an effective means of preventing it." Blanc and Caminopetros, 1922 (original paper in French here) - Material from nine cases of shingles was inoculated into the eyes, cornea, conjunctiva, skin, brain, and spinal cord of a series of animals, including rabbits, mice, sheep, pigeons, monkeys, and a dog. All results were negative. Robertson & Groves, 1924 - Exposed 100 healthy individuals to the bodily secretions from 16 different people suffering from influenza. 0 people of 100 whom they deliberately tried to infect with Influenza got sick That is because Viruses don't cause disease. Bauguess, 1924 - "A careful search of the literature does not reveal a case in which the blood from a patient having measles was injected into the blood stream of another person and produced measles." The problem of the etiology of herpes zoster, 1925 - "Many other authors report entirely negative results following the inoculation of herpes zoster material into the sacrified corneas of rabbits: Kraupa (18); Baum (19); LSwenstein (8), Teissier, Gastinel, and Reilly (20) ; Kooy (21) ; Netter and Urbain (22); Bloch and Terris (23); Simon and Scott (24); and Doerr (25). It is evident, therefore, that the results of attempts to inoculate animals with material from cases of herpes zoster must be considered at present to be inconclusive." Volney S and Chney M.D., 1928 - A study where it is clearly stated that cold is not infectious. Dochez et al, 1930 - Attempted to infect 11 men with intranasal influenza. Not a single person got sick. Most strikingly one person got very sick when he accidently found out that is what they were trying to do. His symptoms disappeared when they told him he was misinformed. L. L. Lumsden, 1935 - “Painstaking efforts were made throughout the studies to obtain all traces of transmission of the disease through personal contact, but it appears that in this outbreak in Louisville evidence of personal association between the cases of poliomyelitis, suggestive of cause and effect, was no more common than that which might have been found if histories had been taken of personal association between cases of broken bones occurring in the city in the same period.” Thomas Francis Jr et al, 1936 - Gave 23 people influenza via 3 different methods. 0 people got sick.. They gave 2 people already "suffering from colds" the influenza who also did not get sick Burnet and Lush, 1937 - 200 people given "Melbourne type" Influenza . 0 people showed any symptoms of disease. 200/0. Lumsden, 1938 - "It is quite usual in small [polio] outbreaks in rural counties for individual cases to develop in separate homes three or for miles apart without there being any evidence of direct or indirect personal contact having operated between persons afflicted." L. L Lumsden, 1938 - ”The general and usual epidemiological features of the disease [polio] all appear opposed to the hypothesis that poliomyelitis is a contagious disease spread among human beings by nose-to-nose or any other direct personal contact.” Burnet and Foley, 1940 - Attempted to experimentally infect 15 university students with influenza. The authors concluded their experiment was a failure. Thomas Francis Jr, 1940 - Gave 11 people "Epidemic Influenza" 0 people got sick. That is because viruses don't cause disease. John Toomey, 1941 - A veteran polio researcher: "no animal gets the disease from another, no matter how intimately exposed." A. R. Kendall, 1945 - “The epidemiological facts of poliomyelitis are these: … (2) A majority of cases of clinically diagnosable poliomyelitis (polioparalysis) occur sporadically, with no history of contact with previous cases. (3) Two cases of polioparalysis in one family are unusual, even though no precautions are taken to prevent cross infection. (4) Clinically diagnosable cases of poliomyelitis (polioparalysis) show little tendency to spread, even in schools or other places of public gathering. (5) Incidence of polioparalysis is no greater among doctors and nurses, in intimate contact with acute cases than it is among the civil population, even though the former are exposed freely to infection.” […] “Polioparalysis is not contagious.” E. B. Shaw & H. E. Thelander, 1949 - “The epidemiology of the disease [polio] remains obscure. There has been a tendency to depart from an early theory that the disease spreads by means of direct contact.” Albert Sabin, 1951 (inventor of the polio vaccine). "There is no evidence for the transmission of poliomyelitis by droplet nuclei." Archibald L. Hoyne, 1951 (alternative link here) - “However, in the Cook County Contagious Disease Hospital where the latter procedure has not been used there has never been a doctor, intern, nurse or any other member of the personnel who contracted poliomyelitis within a period of at least thirty-five years, nor has any patient ever developed poliomyelitis after admission to the hospital.” Ralph R. Scobey, 1951 - ”Although poliomyelitis is legally a contagious disease, which implies that it is caused by a germ or virus, every attempt has failed conclusively to prove this mandatory requirement of the public health law.” Professor of clinical pediatrics and president of the Poliomyelitis Research Institute, Syracuse, N.Y. Ralph R. Scobey, 1952 - "In addition to the failure to prove contagiousness of human poliomyelitis, it has likewise been impossible to prove contagiousness of poliomyelitis in experimental animals." Douglas Gordon et al, 1975 - This study gave 10 people English type Influenza and 10 people a placebo. The study was negative. Most telling is they admit that mild symptoms were seen in the placebo group, proving that the inoculation methods cause them. Beare et al 1980 (refer to reference 6 in the linked paper). Quote from John J Cannell, 2008 as follows - “An eighth conundrum – one not addressed by Hope-Simpson – is the surprising percentage of seronegative volunteers who either escape infection or develop only minor illness after being experimentally inoculated with a novel influenza virus.” Nancy Padian, 1996 - A study which followed 176 discordant couples (1 HIV positive and the other negative) for 10 years. These couples regularly slept together and had unprotected sex. There were no HIV transmissions from the positive partner to the negative partner during the entirety of the study. John Treanor et al, 1999 - Gave 108 people Influenza A. Only 35% recorded mild symptoms such as stuffy nose. Unfortunately 35% of the placebo control group also developed mild symptoms proving the methods of inoculation are causing them. Bridges et al, 2003 - "Our review found no human experimental studies published in the English-language literature delineating person-to-person transmission of influenza... Thus, most information on human-to-human transmission of influenza comes from studies of human inoculation with influenza virus and observational studies." The Virology Journal, 2008 - ”There were five attempts to demonstrate sick-to-well influenza transmission in the desperate days following the pandemic [1918 flu] and all were ’singularly fruitless’ … all five studies failed to support sick-to-well transmission, in spite of having numerous acutely ill influenza patients, in various stages of their illness, carefully cough, spit, and breathe on a combined total of >150 well patients.” Public Health Reports, 2010 - ”It seemed that what was acknowledged to be one of the most contagious of communicable diseases [1918 flu] could not be transferred under experimental conditions.” Jasmin S Kutter, 2018, - Our observations underscore the urgent need for new knowledge on respiratory virus transmission routes and the implementation of this knowledge in infection control guidelines to advance intervention strategies for currently circulating and newly emerging viruses and to improve public health. - There is a substantial lack of (experimental) evidence on the transmission routes of PIV (types 1–4) and HMPV. - Extensive human rhinovirus transmission experiments have not led to a widely accepted view on the transmission route [35, 36, 37, 38, 39, 40]. - However, until today, results on the relative importance of droplet and aerosol transmission of influenza viruses stay inconclusive and hence, there are many reviews intensively discussing this issue [10, 45, 46, 47, 48, 49, 50]. - Despite this, the relative importance of transmission routes of respiratory viruses is still unclear, depending on the heterogeneity of many factors like the environment (e.g. temperature and humidity), pathogen and host [5, 19]. Jonathan Van Tam, 2020 - Conducted these human trials of Flu A in 2013. 52 people were intentionally given "Flu A" and made to live in controlled conditions with 75 people. 0 people sick. 0 PCR positive. J.S. Kutter, 2021 - “Besides nasal discharge, no other signs of illness were observed in the A/H1N1 virus-positive donor and indirect recipient animals.” The animals were subsequently euthanized after the animals experienced what the scientist describe as having breathing difficulties (no further details were given to describe their condition). *Refer to Note 1. Ben Killingley, 2022 - Gave 36 people what he considered to be purified Covid Virus Intranasally. The Results: Nobody got sick. *Refer to Note 2. Notes *Note 1 - Jasmin Kutter, 2021: From the Results section: “Throat and nasal swabs were collected from the donor and indirect recipient animals on alternating days.” This on its own can lead to nasal discharge which is the only “sign of illness” that was noted in this study. *Note 2 - Ben Killingley, 2022: See the video explanation by Jamie here. Ben Killingley also conducted a study in the early 2010's in which he had inoculated people in a room with 75 others some wearing masks others as a control. Not a single person even tested PCR positive. Some links to his previous studies include a 2011, 2019 and a 2020 study. It is assumed that his latest, 2022 study, is a follow up to cover the findings of his previous findings. Some additional notes on the study referenced include: - They gave 10 people the potent nephrotoxin Remdisivir. - They measure sickness by means of a PCR test which isn't indicative of disease because it can tests positive with “asymptomatic” cases as well. - Even if you say that a runny nose after swabbing is Covid. A 50% outcome to a direct challenge of something is a negative result. It doesn't suggest causation which would need to be at least 90%. - The very methods of inoculation used during the study could cause the nasal congestion/discharge (which is their measure of whether someone is sick or not). This has been shown in previous studies. - Lastly nobody was given "regeneron" because nobody got "sick". *Note 3 - Dr Robert Willner, 1994: December 7th 1994 Hollywood Roosevelt Hotel, Greensboro, N.C., Dr Willner (a medical doctor of 40 years experience) an outspoken whistleblower of the AIDS hoax. In front of a gathering of about 30 alternative-medicine practitioners and several journalists, Willner stuck a needle in the finger of Andres, 27, a Fort Lauderdale student who says he has tested positive for HIV. Then, wincing, the 65-year-old doctor stuck himself. In 1993, Dr. Willner stunned Spain by inoculating himself with the blood of Pedro Tocino, an HIV positive hemophiliac. This demonstration of devotion to the truth and the Hippocratic Oath he took, nearly 40 years before, was reported on the front page of every major newspaper in Spain. His appearance on Spain’s most popular television show envoked a 4 to 1 response by the viewing audience in favor of his position against the “AIDS hypothesis.” When asked why he would put his life on the line to make a point, Dr. Willner replied: “I do this to put a stop to the greatest murderous fraud in medical history. By injecting myself with HIV positive blood, I am proving the point as Dr. Walter Reed did to prove the truth about yellow fever. In this way it is my hope to expose the truth about HIV in the interest of all mankind.” He tested negative multiple times. He died of a Heart attack 4 months later 15th April 1995 (yeh right, funny how these naysayers all die suddenly. Link to the presentation here. Ludicrous “Transmission” Studies The picture of virology’s ludicrousy won’t be complete without a list of studies showing the insanity of what virologists claim to be transmission of disease. This include the injection of fluids into the brains and lungs of animals and we may just include some epidemiological studies to show how these are also not proof of anything. Joe Hendry mostly put it together and the papers we have are as follows (*Please note that this section is open to comments at the moment and anyone that want to add notes or studies are free to leave a comment): Louis Pasteur, 1881 - For rabies, tried to demonstrate transmission by injecting diseased brain tissue "directly onto the surface of the brain of a healthy dog through a hole drilled into its skull." Simon Flexner and Paul A. Lewis, 1910 - Spinal cords from deceased children were ground up and emulsified to be injected into the brains of monkeys. Study explained in detail here. John F. Anderson and Joseph Goldberger, 1911 - Injected blood from a measles patient directly into the heart and brains of monkeys. Carl Tenbroeck, 1918 - A mixture of ground up rat's livers, spleens, kidneys, testicles, lungs, hearts, and brains was injected into the brains of other rats. Claus W. Jungeblut, 1931 - Ground up monkey spinal cord was injected into the brains of other monkeys. Wilson Smith, 1933 - “The infected animal is killed when showing symptoms, often at the beginning of the second temperature rise. The turbinates are scraped out, ground up with sand, and emulsified in about 20 c.cm. of equal parts of broth and saline. The emulsion is lightly centrifuged, and about 1 c.cm. of the supernatant fluid is dropped into the nostrils of another ferret.” Thomas Francis and Jr, T. P. Magill, 1935 - Ground up ferret lung tissue was injected into the brains of rabbits. Ann G. Kuttner and T'sun T'ung, 1935 - Ground up kidney and brain of a guinea pig was injected into the brain of another guinea pig. Erich Traub. April 01 1936 - Ground up mouse brain was injected into the brains of guinea pigs. Albert B. Sabin and Peter K. Olitsky, 1937 - Ground up mouse brain was injected into the brains of other mice. G. John Buddingh, 1938 - Ground up chick embryo was injected into the brains 2 or 3 day old chicks. Gilbert Dalldorf, 1939 - Ground up ferret spleens was injected into the brains of mice. Claus W. Jungeblut et al, 1942 - Ground up brain or spinal cord of paralyzed mice was injected into the brains of 13 monkeys. Henry Pinkerton and Vicente Moragues, 1942 - Ground up brain tissue from dying mice was injected into the brains of pigeons. C. Kling et al, 1942 - Injected sewage sludge into the brains and abdomen of monkeys. This convinced him that he had isolated a virus and proven that the sewer is a vehicle for polio transmission. D.M. Horstmann, 1944 - Allegedly "proved" that the feces of polio patients contained "poliovirus" by injecting fecal samples into monkeys' brains and spines. Joseph E. Smadel et al, 1945 - Ground up pigeon spleen was injected into the brains of mice. F. Sargent Cheever et al, 1949 - Ground up mouse brain was injected into the brains of rats and hamsters. Isolation Isolation has been well defined in Virus Lie - The Result of 4 Years of Study and to this day there has not been a single paper presented that could show the isolation of a virus without first contaminating the sample. This is shown in detail in the virus lie article and will not be repeated here again. One interesting point that can be captured here is all the studies showing a control test proving that the isolation method used for viruses is flawed. They can be listed as follows: John F Enders, 1954 - Under other agents isolated during the study. "A second agent was obtained from an uninoculated culture of monkey kidney cells. The cytopathic changes it induced in the unstained preparations could not be distinguished with confidence from the viruses isolated from measles." It is highlighted here. Refer to the video explanation here. Image It is further discussed in the paper that "While there is no ground for concluding that the factors in vivo (in the body) are the same as those which underlie the formation of giant cells and the nuclear disturbances in vitro (outside a living organism), the appearance of these phenomena in cultured cells is consistent with the properties that a priori might be associated with the virus of measles.” Image Rustigian et al, 1955 - This paper is described in an article by Viroliegy here (look under Rustigain in the article). Cohen et al, 1955 - This paper is also described in the same article by Viroliegy here (look under Cohen in the article). Bech and von Magnus, 1959 - This paper is also described in the same article by Viroliegy here (look under Von Magnus in the article). F Rapp et al, 1959 - This paper is described in a video by Spacebusters here. Most noteworthy is “Monkey kidney cells, however, are unsuitable for the investigations of the type reported here; Peebles et al. and Ruckle showed that monkeys, and cell cultures derived from them, are often infected with an agent serologically indistinguishable from human measles virus, which causes cytopathic changes in monkey kidney cell cultures almost identical with those caused by human measles virus.” Image Carl J. O’Hara et al, 1988 - The study demonstrated "HIV" particles in 18 out of 20 (90% of) AIDS-related lymph node enlargements but also in 13 out of 15 (88% of) non-AIDS-related enlargements. Which means that particles claimed to be HIV virions are non-specific since identical particles can be found in the majority of patients with enlarged lymph nodes not attributed to AIDS, and at no risk for developing AIDS. Refer to @Aldhissla45’s tweet here. P Gluschankof et al, 1997 - This paper described in a video here with additional notes by Jamie here. Julian W. Bess Jr., 1997 - This paper described in a video here with additional notes by Jamie here. C.A. Cassol, 2020 - This paper is described by Andrew Kaufman here as well as by Thomas Cowan here. “Unofficially” we can also add the Lanka 3 phase control experiment that can be seen here or searched for it here. A further indication of the isolation procedure fallacy is shown in a study during which the CPE becomes more well defined with the addition of specific substances. The study is as follows: Leon Caly et al, 2020 - “Following several failures to recover virions with the characteristic fringes of surface spike proteins, it was found that adding trypsin to the cell culture medium immediately improved virion morphology.” See a video explanation here. Recent Requests and Statements Further and more recent requests and statements that were sent to me by my good friend Courtenay are as follows: May 5, 2022: U.S. CDC and Agency for Toxic Substances and Disease Registry confirmed that a search of their records failed to find any that describe anyone on Earth finding an alleged “avian influenza virus” in the bodily fluids of any diseased diseased host (animal or human) and purifying “it”… which is necessary so that “it” could be sequenced, characterized and studied with controlled experiments. This can be viewed here. May 20, 2022: Public Health Agency of Canada confirmed that they have no record of any alleged “avian influenza virus” having been found and purified from the bodily fluid/tissue/excrement of any diseased “host” on the planet (in order for “it” to be sequenced, characterized and studied with controlled experiments) by anyone, anywhere, ever. Insanely, they insist that: “Viruses” are in hosts despite their utter inability to find them there,. It’s necessary to “grow them” in non-host cells (as if “they” would grow better there than they allegedly grew in the diseased host lol). They pretend that mixing complex substances together results in purification. This can be viewed here. December 20, 2021: Public Health Agency of Canada confirmed that they have no record of any alleged “virus” having been purified from a sample taken from any diseased human on Earth, by anyone, ever, period. To be viewed here. March 11, 2022: U.S. Centers for Disease Control and Prevention and Agency for Toxic Substances and Disease Registry respond to a FOIA request for all studies / reports in their possession, custody or control describing the purification of any “virus” addressed by any “vaccine” on either their childhood or adult U.S. “immunization” schedule, directly from a sample taken from any diseased "host" on Earth where the sample was not first combined with any other source of genetic material. CDC/ATSDR provided 5 studies on “rotavirus” (thereby admitting they have no records for any other alleged viruses). None of these 5 studies actually describe isolation/purification of a “rotavirus” from a human. Request, response, studies to be viewed here. March 8, 2023: Italy 2020: Inside Covid’s “Ground zero” in Europe - Three years ago the Western World came to a standstill. The official Covid-19 narrative depicted a strange suddenly-super-spreading, deadlier-than-flu virus hailing from China that landed in Northern Italy. On February 20, 2020 the first alleged case of Covid-19 was discovered in the West in the Lombardy town of Codogno, Italy. Later that day the Italian government reported their first “Covid-19 death.” Dramatic media reports emerging from Northern Italy were hammered into and onto the Western psyche giving the impression there was a mysterious “super spreading” and “super lethal” novel virus galloping across the region infecting and killing scores of people. Read the rest of the report here. Conclusion The above list will be worked on over the coming years. If you think that any corrections need to be made or if you want to add additional studies, please leave a comment. Share Leave a comment https://open.substack.com/pub/dpl003/p/virology-the-damning-evidence?r=29hg4d&utm_medium=ios&utm_campaign=post
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