FINISHING THE LAST RESET .... ORPHAN TRAINS https://www.bitchute.com/video/m8Mt88Kf8MQ7/

So You Got Spiked: Now What? Especially important for athletes and future parents: invest in your health, your future & future generations. Dr. Syed Haider Spikehead | Niskia | Flickr I see a lot of patients who have been harmed by COVID and the shots. What I rarely see is anyone who was exposed to the spike protein but still feels perfectly fine: just here for a checkup, doc! Most of my patients did feel perfectly fine for weeks, months and sometimes years after their spike protein exposure, before suddenly coming down with severe symptoms. But in these cases there was ongoing inflammation, spike persistence, perhaps viral persistence, micro clotting, perhaps autoimmunity, alterations in gut bacteria and more that could have been detected far sooner. This is important because it's always easier to prevent illness than to treat illness once it manifests. Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share It takes a lot to push your body out of health and often takes a lot to push your body back into the fully resilient state of health you were in before. This is contrasted with symptomatic, or functional recovery - with Long Haul it’s often relatively easy to get someone back to feeling 90-100% better while they are taking treatments like ivermectin and making some lifestyle changes. What is harder is to get them back to the place of resilience they were at before they got sick: able to eat whatever they want, sleep whenever they want, get by without supplements and meds, etc. I certainly believe it is possible and it does happen, but that complete healing is a harder nut to crack than simply functional recovery dependent on various “crutches”. Obviously part of complete and deep healing is making the often drastic lifestyle changes - because it was the poor lifestyle that got you in trouble in the first place, along with toxic exposures from the environment and food. So ultimately you don’t really want to return to the way things were before you got sick: that would just set you up to get sick all over again. This is confusing for people, because they thought they were fine. I hear this repeatedly: I was so healthy before COVID (or the shot). But when I push a bit it's clear patients were not sleeping enough, were overtraining, under too much stress, having too much caffeine/alcohol, not getting enough sun, spending too much time indoors, online, in front of screens, eating relatively poorly, consuming too many pesticides, seed oils, had leaky gut, autoimmune issues, skin issues, etc. Many patients list no medical problems yet also list a number of medications for psychiatric diseases, hypertension, cholesterol, migraines, erectile dysfunction, etc. We’re hardwired to minimize things, to ignore them and to forget them. Our culture trains us to have high time preference: meaning we prefer the present too much compared to the future. Most people are depleting their reserves instead of building them. Just as most find it difficult to save money or invest for the future, most also find it difficult to invest in their health with exercise, sleep, sun, diet, etc. The millionaire who eats through their savings rather than investing it can live high on the hog for a few years, but eventually the millions run out and then they’re left with nothing. The same happens with our health: youth and health usually go hand in hand and they are a form of wealth that can be used up before its time, or can be conserved and built upon so that it lasts for the long term. So the first thing everyone must do is clean up their act and start investing in their future. The most important wealth is health. Second, anyone who got the shot and thinks they are fine, should still consider doing something to check themselves out: there is a lab panel I order at mygotodoc.com that can be done at a local lab and may be covered by insurance. Register Free at mygotodoc There are more advanced panels we can send to Incelldx to check for spike protein in monocytes and for advanced inflammatory markers. There is an atypical amyloid fibrin microclot score we can order from a specialized pathology lab, and there is Dr Sabine Hazan’s gut microbiome testing that I can order via Progenabiome. There are some supplementary tools as well like tracking heart rate variability, sleep quality, and continuous glucose monitoring that is especially important for those with poor metabolic health, which is most people nowadays. Athletes might especially consider cardiac screening with troponin, BNP, EKG, Echo and perhaps even a cardiac MRI: when sudden death is a possibility even seemingly excessive screening may become sensible. Doctors Taking ER Call: A Dying Breed But the population I worry the most about are women in their reproductive years. Dr James Thorp has spoken out about this at length in interviews and peer reviewed papers. Totality of the Evidence compiles the data currently available. A baseline pre-pandemic miscarriage rate around 12% is already too high and data suggests it has shot up after the vax rollout. VAERS miscarriage reports spiked 4070% post shots. The initial Pfizer trial suggested a rate above 80% based on incomplete data, though it was misreported at the time by using the wrong denominator to hide the alarm. I know what it feels like to lose a baby. It tears your heart out. It’s difficult to forgive yourself for perceived mistakes that may have triggered the pregnancy loss. Share Before pregnancy is a time to build your resources: focus on supercharging your nutrient stores. Eat organ meats, eggs, steak, milk and avoid junk food: no seed oils or sugar and avoid pesticides. Consider plasma donation to cut down body stores of toxic chemicals. Optimize sleep, sun, stress management, body fat levels, and metabolic health. Generally aim to get into the best shape of your life. And if you were exposed to spike protein check to see if you need to detox from it. You can eliminate spike and microclots and inflammation and even autoimmunity triggered by the shots or COVID. If you don’t deal with it before pregnancy you may have to deal with it during pregnancy in the form of long haul or worst case scenario a pregnancy loss triggered by spike, and even after birth your baby may be harmed via spike in breast milk. There is a report in VAERS of a breastfed baby dying soon after its mothers got the shot: One report doesn’t mean it’s only happened once. VAERS is severely underreported, especially for these shots. We should heed the warnings Pfizer gave male trial participants not to go near pregnant women and if having sex with women of childbearing age, to use at minimum two forms of contraception. If anything we have far more data now than we did then to suggest that spike protein exposure is unsafe for everyone and especially those pregnant or breastfeeding. Many of my female patients report altered menstrual cycles and other symptoms whenever they are exposed to those recently vaccinated. Shedding is a real phenomenon and it can wreak havoc on the female reproductive system. Whether or not there is a depopulation agenda we are seeing a dramatic worldwide drop in live birth rates. Sperm counts have dropped, female fertility is at all time lows, and miscarriage rates have shot up. There are simple solutions that can accomplish short term goals of fertility and symptom relief and there are more comprehensive lifestyle based solutions that solve the underlying problems for the long term. Free Lifestyle Ebook/Webinar/Course Invest in yourself and your children for the long run and you won’t be sorry. https://blog.mygotodoc.com/p/so-you-got-spiked-now-what https://telegra.ph/So-You-Got-Spiked-Now-What-04-02

A compilation of corporate media’s explanation of sudden deaths Rhoda WilsonMarch 22, 2024 As sudden deaths and cardiovascular diseases became more common, corporate media has needed to find explanations for the alarming trends. Filipe Rafaeli has compiled corporate media headlines that provide the most curious explanations. Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox… The list of reasons for increased sudden deaths and strokes, according to the mainstream media By Filipe Rafaeli In the initial study of the Pfizer vaccine, published in the New England Journal of Medicine, with around 44,000 people, with 22,000 in the placebo group and about 22,000 in the vaccine group, more people died from all causes in the vaccine arm than in the placebo arm. Initially, it was 15 to 14. Shortly after, when updating this number at the Food and Drug Administration, the US regulatory agency, the number changed to 21 to 17. Now, without any surprise, in the most recent update, it’s already 22 to 16. “Most importantly, we found evidence of an over 3.7-fold increase in number of deaths due to cardiac events in the BNT162b2 [Pfizer-BioNTech] vaccinated individuals compared to those who received only the placebo.” wrote the scientists in the latest update. After the mass application of the product, an excess of population mortality was recorded. In The Lancet, the world’s most impactful scientific journal, they analysed UK data: a 7.2% excess in 2022 and an 8.6% excess in 2023. The highlight? Cardiovascular diseases. The comparison is with the 5 previous years. And do you know what is the most interesting thing in this Lancet analysis? It’s the increase in deaths at home, that is, sudden deaths. There wasn’t even time to go to the hospital. There’s an impressive 22% increase. US life insurance companies, the ones paying the bills, also found the same thing: more deaths in younger people since 2021. Well, since everyone is seeing many people suddenly dying and others with cardiovascular diseases, the mainstream media needed to talk about heart attacks and sudden deaths. It made headlines. They needed to explain. Normalisation Here, the collection of headlines in the national and international mainstream media with the most curious explanations since 2021. According to Wales Online, from Wales, what is causing heart attacks is the increase in electricity bills: Energy bill price rise may cause heart attacks and strokes, says TV GP – Wales Online On the other hand, the Express from the UK claims that the cause of heart attacks is heavy metal and techno music: Atrial fibrillation: Two music genres linked to ‘potentially dangerous’ heart arrhythmias In Revista Veja, from Brazil, the cause of heart attacks is attributed to global warming: With a warmer world, the impact of climate change on health increases However, according to CNN Brazil, the real culprit isn’t heat but cold: Cardiovascular diseases can increase by up to 30% in winter; see precautions For the Daily Mail, from the UK, it is indeed the cold, but the issue arises only if you remove the snow: Expert warns that shovelling snow can be a deadly way to discover underlying heart conditions In The Times of India, the blame isn’t on the cold, but on the heat, along with humidity: Heart attacks more frequent when heat, humidity high: Study | Ahmedabad News In The Guardian, from the UK, the blame is actually on rain: Floods linked to increased deaths from heart and lung disease, Australian-led research shows In the Express, from the UK, it has nothing to do with the weather. The culprit for heart attacks is dirty dishes: Washing up helps wipe out heart risk In the UK’s Express, the mystery is solved. Skipping breakfast is blamed for heart attacks: Heart attack: Does skipping breakfast increase your risk? According to The Sun, from the UK, the reason for the excess of heart attacks is because you poop too much: RISK FACTOR How often you go to the toilet every day can ‘predict your risk of heart attack’ In The Times, from the UK, the cause of heart attacks is being single: Lonely older women at greater risk of heart attack, study shows However, according to Wales Online, from Wales, the reason people die suddenly is the opposite. It’s because people are dating: Average age of sudden death during sex is 38 – why it happens – Wales Online On the other hand, The Independent, from the UK, explains that the real cause is troubled relationships: A happy relationship enhances heart health, claims new study | The Independent According to News19, from the US, the cause of increased heart attacks is breaking up: Doctors say ‘Broken Heart Syndrome’ is real, and it can be deadly | WHNT.com In Isto é, from Brazil, the cause of cardiovascular problems is not exercising and watching too much TV: Watching TV can increase the risk of blood clots, study suggests However, The Irish Times, from Ireland, says the opposite, that the culprit is exercising: Physical activity may increase heart attack risk, study suggests – The Irish Times According to the British Heart Foundation, the cause is improper sleep. It’s because people sleep too little or too much: Does sleeping too little or too much raise your risk of heart disease? – BHF In The Sun, from the UK, the cause is indeed related to sleep, but because of daylight saving time: Moving clocks forward an hour could be dangerous for millions of Brits with serious heart problems – The Sun Meanwhile, for Canaltech, from Brazil, the culprit of heart attacks isn’t daylight saving time, but rather illuminated light: Sleeping with lights on increases the risk of heart disease and diabetes; understand For the Express, from the UK, the cause of heart attacks is “low-fat” processed foods: Heart attack: The ‘healthy’ food which may ‘put you at risk for heart disease’ – avoid According to The Standard, from the UK, what’s causing heart attacks is stress: Thousands facing heart problems due to ‘post-pandemic stress disorder’ | Evening Standard In the North Wales Chronicle, from Australia, the culprit of heart attacks is artificial sweeteners: Artificial sweeteners found in diet drinks could increase risk of heart attack – research | North Wales Chronicle In The Sun, from the UK, scientists have recently discovered the culprit. It’s the common cold: Common cold can trigger a killer blood clot disorder, scientists discover for the first time | The Sun The Express, from the UK, blames obsessive-compulsive disorder for strokes: Stroke: People with a common disorder could be ‘three times’ more likely to have a stroke In the UK’s Express, the culprit is the gluten-free diet: Heart attack: A gluten-free diet could increase the risk | Express.co.uk According to The Scientist, from the US, the culprit of heart attacks and strokes is noise from cars, airplanes, and trains: How Environmental Noise Harms the Cardiovascular System | The Scientist Magazine® According to UOL, from Brazil, the culprit for the increase in heart attacks and strokes is elections: How elections increased cases of heart attack and stroke in the US: is there the same risk in Brazil? In the New York Post, from the US, sudden infant deaths are caused by video games: Video games could trigger deadly heart problems in children: study According to Today, from the US, sudden infant deaths are actually common occurrences: All kids should be screened for possibility of sudden cardiac arrest, group says According to Today, from the US, the cause is that people are angry or emotionally disturbed: Stroke may be triggered by anger, upset or intense exercise in the hour before In the UK’s Daily Mail, the cause of heart attacks is said to be sun exposure for just one day: Sunbathing for just ONE DAY may increase your risk of heart disease – and stop the body fighting infections, study suggests However, according to The Times UK, all of the above are wrong. It’s only known that it’s happening, but the reason is a mystery: Mystery rise in heart attacks from blocked arteries The US-based New Scientist confirms it is indeed a mystery. Nobody knows the reason: There are thousands more UK deaths than usual and we don’t know why | New Scientist And even though it’s a mystery, and therefore could be anything, absolutely anything, the Brazilian Government has already assured me that one thing, at least, is not the cause: It’s false that Covid-19 vaccines cause sudden illness Although nobody should worry too much, because according to the US-based health and science website Revyuh News, it’s actually beneficial to have a heart attack: New Study Reveals Shocking Benefit of “Heart Attack” About the Author Filipe Rafaeli is a filmmaker and four-time Brazilian aerial acrobatics champion. He publishes articles on a Substack page titled ‘Pandemia’ which you can subscribe to and follow HERE. The Expose Urgently Needs Your Help... Can you please help power The Expose’s honest, reliable, powerful journalism for the years to come… Your Government & Big Tech organisations such as Google, Facebook, Twitter & PayPal are trying to silence & shut down The Expose. So we need your help to ensure we can continue to bring you the facts the mainstream refuse to… We’re not funded by the Government to publish lies & propaganda on their behalf like the mainstream media. Instead, we rely solely on our support. So please support us in our efforts to bring you honest, reliable, investigative journalism today. It’s secure, quick and easy… Just choose your preferred method to show your support below support Lawyer, Dr Reiner Fuellmich asks to Be Released From Jail With an Electronic Anklet. While you were distracted by the “Where’s Princess Kate Conspiracy”, Deagel’s Depopulation Forecast was confirmed by Heavily Censored Pfizer Documents It’s all over for the Anthropocene, the official geologic period of human-caused climate change The List of Reasons for Increased Sudden Deaths and Strokes, According to the Mainstream Media. https://expose-news.com/2024/03/22/corporate-medias-explanation-of-sudden-deaths/

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🚨 WARNING: Self-Spreading Vaccines Are Approaching Fast! This technology was ALMOST ready to be deployed for COVID-19. So, don't think that global health authorities wouldn't use it in the event of another pandemic. The only thing stopping the mass use of this technology is this pesky thing known as informed consent — but do you think they actually care about that? The whole idea behind self-spreading vaccines is grounded in circumventing "behavioral barriers." Just listen to their own words: "Infectious disease control faces significant challenges including: how to therapeutically target the highest-risk populations, circumvent behavioral barriers, and overcome pathogen persistence and resistance mechanisms." — Timothy Notton et al. The U.S. military and DARPA have also been researching self-spreading vaccines, with DARPA exploring antivirals to "evolve" in real-time against new viral strains. However, if a self-spreading vaccine mutates in an unforeseen way, it could potentially pose grave risks for the entire population. Attorney Aaron Siri issued this statement on the matter: "What might even be the biggest victim ... if they ever release this thing, it's going to be civil, individual rights... "Here, they're going to release a product where you're going to have no choice effectively but to take it. That is the ultimate crushing of individual and civil rights." Watch and listen to this important video from @HighWireTalk. https://x.com/vigilantfox/status/1761141648241664316?s=46

Does History Change? A simple cartoon from 1892 with a possibly a much deeper meaning. Are we stuck in an endless loop of pre-programmed cycles? When pondering this 1892 cartoon, we cant help but think of Coney Island and the orphan trains than ran until 1929. Did they really give venom to our not so distant ancestors, and then repopulate with new uninformed generation? We can help also remembering the asylums which went from cure to incarceration, did these people simply disagree with the new world view? What do you think? Funny cartoon or sinister message… Join us: t.me/HISTORY

How British ‘charities’ are aiding Israeli genocide in Gaza Thursday, 01 February 2024 7:54 AM [ Last Update: Thursday, 01 February 2024 8:33 AM ] By David Miller The genocide in Gaza is being perpetrated by the so-called ‘Israel Defense Forces’. The whole world is appalled. Yet, in the UK, there are organizations raising money to support the genocidal occupation forces. The Association for Israel’s Soldiers is based in occupied Palestine and claims to be the sole avenue through which donations can be made directly to IDF soldiers and IDF units. These donations come from Zionists in Palestine as well as from the US, Canada, Brazil, Mexico, France and the UK. The UK Friends of the Association for the Wellbeing of Israel Soldiers (AWIS) is a registered charity that is obliged by law to show public benefit. Its charitable objects include relief of need and suffering, advancement of education and provision of facilities for recreation of the occupation forces. It does this by providing Mobile Synagogues, recreational facilities for injured genocidaires, free holidays, free student scholarships, mobile Gym and rest and recreation facilities. Among the benefits are swimming pools including the one promoted in a video on Facebook in May last year. In the video, AWIS says they “created a swimming pool in the heart of the desert for the training base of the artillery corps.” Meanwhile, drinking water for Gaza has been cut off for more than three months. Each year, AWIS also puts on an “enlistment festival” for 30,000 recruits to the genocidal occupation forces. Guidance published by the Charity Commission states that it is a legal requirement that “any detriment or harm that results from [charitable purposes] must not outweigh the benefit.” Perhaps supporting genocide outweighs those purposes? Among the Trustees of the charity is Colonel Richard Kemp, a former British soldier said to have hateful views on Islam and Muslims. In December, the BBC was criticized for interviewing Kemp without reference to his role as a UK-AWIS trustee. In one recent interview with a pro-Israel blog, Kemp was quoted as describing the killing of civilians in Gaza as “necessary”. Another trustee is Josh Swidler, who is in the financial industry at a firm called Teamshares. Emphasizing the link between Zionists and Islamophobia, it turns out that Swidler was formerly one of the two directors of Henry Jackson Society Inc., the US fundraising arm of the Islamophobic British think tank. Research for Palestine Declassified, where I am the producer, has traced around twenty British charities that have donated to UK AWIS over the last twenty years. When we examined them we found that they tend to donate to a variety of Zionist causes. In particular, we looked to see which of the recipients directly supported the occupation forces, the so-called “Israel Defense Forces”, illegal settlements, Jewish supremacist sects, or Islamophobic think tanks. These four categories are a sort of Zionist funding bingo. Our research is presented in a table on our investigative Wiki database Powerbase under the title: “UK AWIS - supporters”. The data points there also link to profiles of each of the charities on the Powerbase website as well as the principal individuals involved and how they made their money. The list of charities is as follows: A. M. Charitable Trust C H (1980) Charitable Trust David and Ruth Lewis Family Charitable Trust Denise Cohen Charitable Trust G. R. P. Charitable Trust Gerald and Gail Ronson Family Foundation Jack Goldhill Charitable Trust Lawson Beckman Charitable Trust Loftus Charitable Trust Family Foundations Trust R and S Cohen Foundation Rosenblatt Family Charitable Trust Stanley and Zea Lewis Family Foundation The J E Joseph Charitable Trust The Locker Foundation The Maurice Hatter Foundation The Peltz Trust (Dissolved June 2023) The Phillips and Rubens Charitable Trust The Phillips Family Charitable Trust Wigoder Family Foundation Of the twenty charities we have named which donate to AWIS, five in total have a “full house” sending money to at least one of each of the four categories of funding. We discuss these here at greater length. Gerald and Gail Ronson Family Foundation which was created by Gerald Ronson, the convicted fraudster who runs Rontec, a company that operates over 250 BP and Esso service stations in the UK. These should be an urgent target for the BDS movement. Ronson also set up the Community Security Trust that runs point of the Zionist regime in the UK, spies on anti-Zionist Jews and deliberately confuses anti-Semitism and anti-Zionism in line with the policies of the Zionist regime. Ronson has collaborated with Mossad for decades, through the CST (created in 1994) and before that its predecessor, the Group Relations Educational Trust. One of the charitable objects of the CST is that it will ‘promote research’ and ‘promote public education about’ extremism. In practice, however, Ronson promotes extremism via his family foundation. Among recipients of funding, in addition to AWIS, are: The extreme Chabad sect, which Ronson has been supporting for over 40 years. The Jewish National Fund and the Jerusalem Foundation, both of which are engaged in supporting ethnic cleansing and illegal settlement activity in Palestine. Islamophobic think tanks Civitas and Policy Exchange. These donations are further evidence that Ronson in practice supports extremism and genocide, rather than opposing them. Loftus Charitable Trust, set up by the Loftus family, which made its money from the watchmaking firm Accurist. The family sold the firm to Sekonda in 2014. As well as AWIS, it also funds the extremist Zionist sect Chabad Lubavitch and the Islamophobic think tank Henry Jackson Society. An interesting sign of the small and connected world of the Zionist business class is that the owner of Time Products, the parent of Sekonda to which the Loftus family sold Accurist, is one Marcus Margulies. His family foundation also funds illegal settlements via the Jerusalem Foundation, to which it gave £2.25 million in 2021. The Loftus Trust also gives to a long list of genocidal Zionist groups including the Community Security Trust, Jewish Leadership Council, Mitzvah Day, Stand With Us, UK Friends of IDC (the only private university in ‘Israel’), UKLFI Charitable Trust (which supports the lawfare group UK Lawyers for Israel), Union of Jewish Students, United Jewish Israel Appeal, Zionist Federation David and Ruth Lewis Family Charitable Trust, set up by the Lewis family which owns the River Island clothing chain. The charity also funds Islamophobic think tank, Policy Exchange and illegal settlements via the Jerusalem Foundation and the Jewish National Fund. In addition, the trust funds a range of extremist Zionist groups including Campaign Against Antisemitism, Community Security Trust, Jewish Leadership Council, Palestinian Media Watch, One Voice Europe, and United Jewish Israel Appeal. The Family Foundations Trust, set up by the UK property investor Richard Mintz. The charity has funded UK AWIS and another charity supporting the IDF – Beit Halochem, which we will discuss below. It has also funded the extremist sect Chabad-Lubavitch, the Islamophobic think tank Henry Jackson Society, and the Community Security Trust. Richard’s son and charity trustee Joshua co-founded the website Friend-a-Soldier, an online platform where soldiers can become ‘digital ambassadors’ for the occupation forces. Phillips & Rubens Charitable Trust, set up in 1969 by the accountant Michael Phillips and his wife Ruth. Phillips was at that time a partner in the accountancy firm Hacker, Rubens, Phillips & Young, which he ran with the late Stuart Young. Stuart Young would later be appointed chairman of the BBC by Margaret Thatcher, and was the brother of David (later Lord) Young who at one time chaired the board of trustees of The Peter Cruddas Foundation, which has funded the anti-Muslim think tank Policy Exchange. Lord Young and Michael Phillips were also both trustees of the Stuart Young Foundation along with the solicitor Martin Paisner, who is also a trustee of the Phillips & Rubens Charitable Trust and a large number of other Zionist and/or conservative foundations. The charity has donated to the occupation forces via AWIS from as early as 2009. It has also donated to British ORT, an “education” grouping that trains staff both in Israeli arms firms and in the occupation forces in “Israel”. It supports illegal settlements and ethnic cleansing in East al-Quds (Jerusalem) via the Jerusalem Foundation and Yad Sarah, and supports the Jewish supremacist Lubavitch Foundation and the following Islamophobic think tanks: Centre for Social Cohesion, Civitas, Henry Jackson Society. Naturally, it also supports a range of (Zionist) Synagogues (e.g. United Synagogue) and lobby groups including the United Jewish Israel Appeal and the Union of Jewish Students. UK AWIS is already under investigation by the UK charity regulator the Charity Commission. The investigation should widen to include the nexus of genocide-supporting charities revealed here. They should be shut down by the Charity Commission. In addition to AWIS, Zionist occupation forces are provided with millions in funding every year by other charities. These charities are almost wholly unknown. Palestine Declassified has unearthed new details on one of these charities called Beit Halochem. It is dedicated to raising money for what it calls ‘our’ heroes who have ‘fought’ to ‘protect the state of Israel’ – meaning members of the genocidal occupation forces currently engaged in mass killings in Gaza and throughout Palestine. Charitable objectives of the charity include the relief of ‘Adverse physical and mental effects suffered by individuals in Israel’. It doesn’t say so, explicitly, but it’s clear that the individuals noted do not include Palestinian civilians. As Beit Halochem says, its name ‘literally means “House of Warriors”.’ This racism in the application of its ‘public benefit’ is one reason why this charity should be shut down by the UK Charity Commission. Another is that it violates the harm principle – the harm of supporting genocide clearly outweighs the benefit of rehabilitation of injured genocidaires. The Chairman of the charity is Andrew Wolfson, of the hugely wealthy Wolfson family. The family is best known for its ownership of the Next retail empire. Here is a picture of him with the genocidal president of ‘Israel’, Isaac Herzog, and the extremist advocate of the settler movement, the ambassador to London Tzipi Hotevely. The Charles Wolfson Charitable Trust is named after his grandfather who died in 1970. Other trustees include his brother (Lord) Simon Wolfson, the Chief Executive of Next plc, and (Lord) Jon Mendelsohn, a key Israel lobby actor. The charity has donated over £600,000 to Beit Halochem since 2018. The charity also helps to encourage racism against Muslims by funding Islamophobic think tanks such as Civitas and Policy Exchange. It also funds the Jerusalem Foundation which is directly engaged in settlement activity and ethnic cleansing in East Al-Quds. Research for Palestine Declassified reveals that Beit Halochem receives funds and support from a range of other Zionist family foundations including the aforementioned Denise Cohen Charitable Trust, Family Foundations Trust, Gerald and Gail Ronson Family Foundation, Loftus Charitable Trust, and The Locker Foundation, all of which also fund UK AWIS. Other charities involved include The Pears Family Charitable Foundation, Exilarch’s Foundation and Bluston Charitable Settlement. Here are some details on each of these three charities: The Pears Family Charitable Foundation is run by the Pears brothers once voted the worst landlord in the UK by viewers of a BBC consumer program. Their charity also funds Islamophobic think tank Civitas and Policy Exchange, the Zionist Council of Christians and Jews, the Jewish Leadership Council, the Union of Jewish Students, the United Jewish Israel Appeal, and normalizing charities including Mitzvah Day UK, Solutions Not Sides, The Abraham Fund Initiatives. It has also funded the extreme ultra-Zionist Chabad sect, recently in the news for the illegally dug tunnels underneath their global HQ in New York. The Exilarch’s Foundation is run by David Dangoor, the property magnate who runs property firm Monopro which registered £121.9m assets in 2017-18. His foundation also funds the Islamophobic think tank Henry Jackson Society and ethnic cleansing in East al-Quds, via the Jerusalem Foundation as well as the Community Security Trust, the Faith and Belief Forum, the Tony Blair Institute, the Union of Jewish Students, the pro-Israel Jewish Leadership Council and the United Jewish Israel Appeal, the largest Zionist charity in the country. Bluston Charitable Settlement is run by Anna Josse, who co-runs private equity firm Regent Capital having established and run the Zionist foundation the New Israel Fund UK in the 1990s. She also helps to run Prism the Gift Fund which is a charity that operates and acts for a range of Zionist and other charities. Josse is a Manchester University graduate (after a stunt at a seminary in Israel) and former JSoc chair. She also worked at the Social Market Foundation think-tank. In addition to funding genocide via Beit Halochem, Bluston funds ethnic cleansing via the Jerusalem Foundation in occupied al-Quds and the Jewish National Fund. Among the testimonials on the Beit Halochem UK website is one from Ian Austin, the extreme Zionist and former Labour MP who has displayed a profile picture on X referring to Gaza with the words “Let Israel finish the job”. There are also tributes from the Board of Deputies, the Chief Rabbi and even Israel’s settler-supporting genocidal ambassador to the UK Tzipi Hotevely. Overall, Beit Halochem is devoted to supporting the genocidal Israel occupation forces in Gaza in what appears to be breaches of UK charity law. We will pass the evidence we have unearthed to the UK Charity Commission. https://www.presstv.ir/Detail/2024/02/01/719268/How-British-charities-aiding-Israeli-genocide-Gaza https://donshafi911.blogspot.com/2024/02/how-british-charities-are-aiding.html

The COVID-19 Vaccine Antigen Is ANTHRAX Dr. Ariyana Love By Dr. Ariyana Love Covid-19 vaccines use self-replicating, programmable nanotechnology and synthetic, modified RNA (modRNA) otherwise known as Spike Protein. We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” but what if the Covid-19 vaccine antigen is ANTHRAX? “…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.” Anthrax was developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene” into the highly deadly Bacillus Anthracis bacteria. This means that Cross-Species-Genomics capability was acquired by governments before 1950. A lethal bacterium and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax. Russia’s Anthrax could be treated with antibiotics even several days after exposure, and thus it met the requirements under the Biological Weapons Convention. A bioweapon of choice, Anthony Fauci decided to increase Anthrax lethality and the NIH began genetic attenuation before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more. According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast). Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.” The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks, but we already know that the D.O.D spearheaded this “Covid-19 vaccine” roll-out. Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”. Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014, creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible. Simultaneously, in 2014 China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study revealed severe side effects. PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare. In March 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more. Anthrax causes hemorrhaging. So does Ebola and Marburg. Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs. Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop the Anthrax from replicating inside the human body after inoculation due to it being antibiotic resistant. The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquito which is part of DARPA’s weaponized insect project called The Sentinels. Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax. Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero SPIKE PROTEIN IS AEROSOLIZED ANTHRAX There are 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.” The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine”. “The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.” The above quote from the Recombinant Anthrax Vaccine patent reveals that the poisonous Anthrax “antigen” is being used to genetically modify the genome of humans (cellular entry into humans). By cleaving to the amino termini, protein kinases 1 and 2 are inactivated. This is accomplished by genetic deletions. The molecular basis of Anthrax “vaccines” includes “spores and DNA plasmids” that are entering human cells. The following quote about the Anthrax “protective antigen” is particularly revealing: “PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).” Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”. Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want, including bacteria. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery with contaminated PCR swabs, the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized. This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic. This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality. ALHYDROGEL According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is a DARPA weapon system called Alhydrogel. Hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health. In the Alhydrogel invention, Anthrax was fused together into a nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”. In layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death. Alhydrogel is infused with 750 μg of aluminum, making it magnetic. Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network. Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There are many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system. This Alhydrogel patent demonstrates it’s use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability. This begs the question, where do venereal diseases come from? This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel. “Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA. Both nanoparticles and Anthrax have been used in vaccines for decades already, without the Informed Consent of the public. Alhydrogel was improved and transformed into the Nanoalum adjuvant. Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor. Alhydrogel is also carried in the lipid coating of nanoparticles. The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites. Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector! ANTHRAX SYMPTOMS AND TREATMENT Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and contaminated PCR swabs. Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements (antibiotic resistance). Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans, it’s extremely toxic and will be rejected by our immune system 100% of the time. Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a horrific disaster. U.S. Army statistics that were never published, show the Anthrax “vaccine” induces turbo cancers. The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis and Pericarditis? Anthrax also coagulates the blood. “Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.” Read more here and here. Anthrax induces hemorrhaging. So this explains all the excessive bleeding people have experienced over the last 4 years, following Covid-19 inoculation and from aerosolized exposure, otherwise known as the “shedding” phenomenon. This is a result of Inhalation Anthrax. It becomes clear that the newly dubbed “White Lung Syndrome” and the Chinese ‘pneumonia’ outbreak is none other than Inhalation Anthrax. Mycoplasma pneumonia is on the rise, and it’s listed on Pfizer’s internal documentation as a known Adverse Effect of the Covid-19 inoculation. This study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms this phenomenon is Mycoplasma Pneumonia. All naturally occurring bacterium have cell walls. Mycoplasmas are spherical to filamentous cells with no cell walls. It’s genetically manipulated in a laboratory by GAIN-of-Function for the purpose of enhancing replication inside the human body, making it more lethal. Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by proinflammatory cytokine signaling and histological lesions in the spleen. Anthrax has already been tested on the public. According to the NIH, Anthrax spores were intentionally released into “some environments” in NYC during 9/11. According to the NIH, the FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI. Heroine users in Europe have been tested with Injection Anthrax. Our skies are sprayed with smart dust and chemicals daily. Our governments have launched an all-out war against their constituents. We are being poisoned in a myriad of ways, so please keep this in mind: “Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by World Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.” TREATMENT If you have been inoculated with Covid-19 or PCR swabbed, and you are suffering from heart pain, unusual bleeding, skin rashes and abrasions, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated”, then you may have been exposed to Inhalation Anthrax. Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. Since October 4th, I have received many reports of a red eye syndrome where the entire eye is blood-red. This makes sense because eye tissue is more sensitive. If you have been exposed to Inhalation Anthrax, you may feel hot and severely flushed, and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning. Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need an effective natural medicine detox protocol. I have been successfully detoxing people from the Covid-19 bioweapons for three years. Since I began treating people presenting with Anthrax poisoning with strong antibacterials, my clients are experiencing quicker detox results. If you would like to schedule a consultation with me, please do so through my online booking system. Please follow me on Telegram @drloveariyana and X @drloveariyana. If you would like to donate to my research, please do so here. UPDATE: My Anthrax article is now fully edited and published on Substack. Please review and SHARE. The Covid-19 Vaccine Antigen Is ANTHRAX Read more: https://open.substack.com/pub/drloveariyana/p/the-covid-19-vaccine-antigen-is-anthrax?r=2juwfo&utm_campaign=post&utm_medium=web&showWelcomeOnShare=true https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html

Vaccines Could Affect Mortality and Risks of Other Diseases: Study A recent review found non-live vaccines tend to increase a person’s risks of all-cause mortality, as well. Vaccines Could Affect Mortality and Risks of Other Diseases: Study (OSORIOartist/Shutterstock) Apart from potentially preventing a particular disease, vaccines may cause persistent nonspecific effects that can affect a person’s lifetime survival. In a review published on Dec. 26, 2023, in Vaccine, researchers found that non-live vaccines such as influenza, COVID-19, hepatitis B, and diphtheria-tetanus-pertussis (DTaP) tend to cause adverse nonspecific effects (NSE), increasing a person’s risks of all-cause mortality and infections from other diseases. A live vaccine contains a weakened form of the pathogen, which is less virulent but capable of replicating in the body, thus mimicking the actual disease progression. Non-live vaccines use inactivated viruses, fragments, or genes of the pathogen to trigger an immune response without pathogen replication. Live vaccines elicit a much stronger immune defense, typically requiring only one shot, while non-live vaccines result in a weaker response, often necessitating multiple shots. So far, research has identified several non-live vaccines that cause adverse NSEs, namely DTaP and Tdap, influenza H1N1, malaria, hepatitis B, inactivated polio, and COVID-19 mRNA vaccines. The Vaccine study singled out DTaP, influenza, malaria, hepatitis B, and COVID-19 mRNA vaccines. On the other hand, live vaccines such as the oral live polio vaccine, the Bacillus Calmette-Guérin (BCG) vaccine for tuberculosis, and the smallpox vaccines all have beneficial NSEs, according to the study. “Live vaccines ... elicit epigenetic alterations that train the innate immune system and increase immunity to unrelated infections. In opposition, non‐live vaccines may promote ‘tolerance’ that increases susceptibility to unrelated illnesses,” the authors suggested. The study was primarily based on decades of work from Danish researchers Dr. Christine Stabell Benn and Peter Aaby. “Our work is a tribute to their great scientific work that has not been recognized,” biologist Alberto Rubio-Casillas, one of the study’s authors, told The Epoch Times. Non-Live Vaccines Are Like ‘Ill-Prepared’ Army “Historically, we’ve thought about the innate immune system as the first line of defense,” Dr. Benn told The Epoch Times. It was thought that innate immunity couldn’t store memory. To use war as an analogy, the innate immune system’s “army” couldn’t learn from previous battles with pathogens. Adaptive immunity, on the other hand, could learn and be trained, forming antibodies to fight against the infection. Therefore, for a long time, vaccines were evaluated based on their effects on the adaptive immune system, and antibodies were measured following vaccination. However, researchers in the Netherlands have since shown that the innate immune system can be trained. After vaccinating people with the BCG vaccines and harvesting some of the patients’ innate immune cells, researchers found that after vaccination, the innate cells exhibited a more robust immune response and demonstrated improved clearance of tuberculosis, as well as other bacteria and fungi, when compared to patients’ prevaccination status. However, the opposite was shown for non-live vaccines. Thus, the innate immune system actually does learn something from its previous battles. This is called trained innate immunity. Live vaccines, which mimic an actual disease, enhance the effectiveness of the innate immune system in defending against infections. Non-live vaccines, on the other hand, weaken the immune system’s ability to fend off infections. In a TED talk, Dr. Benn compared infections to a competitive tennis match and live vaccines to a tennis coach. The tennis coach may change tactics and strategies, training the body to have “a wide variety of tricks” against the pathogen. Non-live vaccines, however, are like tennis ball machines that shoot out balls at a specific speed and spot. If a person only trains with a tennis ball machine, he or she will be less prepared for an actual match. “So you may be ill-prepared and even worse off when a real opponent enters the court, and the balls start coming and hitting elsewhere than what you trained for,” Dr. Benn said. Nonspecific Effects Some vaccines result in positive NSEs, but others may result in overall adverse NSEs. The order in which vaccines are administered also factors in. While non-live vaccines cause negative NSEs, administering a live vaccine after a non-live one neutralizes negative NSEs, Dr. Benn said. This has been shown in studies evaluating the safety of measles vaccines, which are often given at about the same time as DTP, a non-live vaccine. Studies have found that if the measles vaccine is given after the DTP vaccine, there is an overall positive effect, whereas if this order is reversed, then there is a negative effect. “It seems that effects are strongest as long as the vaccine is the most recent vaccine,” Dr. Benn said. Dr. Benn added that the BCG vaccine has long-term beneficial NSEs “in spite of other vaccines being given afterward.” The DTaP vaccine has arguably the most evidence of adverse NSEs. Girls who took the DTaP vaccine had a 50 percent higher risk of dying than boys who took it. Compared to girls who were DTaP-unvaccinated, vaccinated girls’ risk of dying was more than 2.5 times higher. Dr. Benn’s studies have generally shown that girls are at a greater risk of developing adverse NSEs after being administered non-live vaccines. Live Vaccines Replaced With Non-Live Vaccines Non-live vaccines are increasingly replacing live vaccines. For example, live oral polio vaccines are no longer available on the U.S. market, and a non-live version is administered instead. This substitution of live vaccines with non-live can pose potential health risks to the general immunity of the population, as the immune systems become less trained and potentially “lazy,” Dr. Benn said. However, the main reason non-live vaccines are preferred over live vaccines is that they’re believed to be safer for people with depleted immune systems. Since a live vaccine causes mild disease in the body, people with acquired immunodeficiency syndrome can develop a disease from the injection and may die since their bodies are unable to clear infections. Conversely, non-live vaccines comprise only disease components, so they can’t induce disease. In this aspect, the “risk of getting the real disease with the live vaccines has been seen as a bigger threat than I think it deserves,” Dr. Benn said. Research suggests that people with weaker immune constitutions because of age or chronic disease may sometimes benefit from having their immune systems trained using live vaccines. In one study involving hospitalized older patients randomized to get the BCG vaccine or a placebo, the incidence of disease among those who took the BCG vaccine was about half the incidence of disease in the placebo group. Health Authorities Still Skeptical Despite the evidence suggesting the potential superiority of live vaccines, Dr. Benn’s research has been largely unacknowledged by the mainstays of academia. “In my interpretation, whereas most researchers now acknowledge nonspecific effects, the major health organizations are reluctant to accept our findings because [the findings] imply the possibility that some vaccines may sometimes be harmful. So it is easier just to dismiss the whole thing,” she said. “The vaccine skeptics, on the other side, may find that our observations on non-live vaccines confirm their worst fears—vaccines can be harmful—but they may be more reluctant to accept the beneficial effects. And their focus on the negative effects may make the vaccine supporters take an even more rigid stance.” Immunologists now largely agree that some vaccines cause NSEs, but how these effects should be quantified remains controversial. This is because the NSEs of vaccines are dependent on context, whereas a vaccine’s specific effects are generally considered context-independent. For example, females may make more antibodies than males, and younger people more than older, but most people still get some form of immunity. “In contrast, because the nonspecific effects act on the broader innate and general immune system, they are dependent on other factors going on in the immune system ... like other health interventions that can alter and modify the nonspecific effects,” Dr. Benn said, noting that not everybody will have the same benefit. Additionally, pharmaceutical companies may be more reluctant to produce live vaccines because they’re harder to culture and manufacture. “If you have ever tried to bake with sourdough, it’s a little bit like live vaccines; they are very dependent on the temperature of the room, the water used to culture it, and so on,” Dr. Benn said. “But basically, all the live vaccines I’m talking about—they have no patents anymore, they’re super cheap to produce, and it’s some of the cheapest vaccines we have to make.” Vaccine Safety: NSEs Versus Adverse Events Though live vaccines tend to cause positive NSEs, that isn’t to say they can’t potentially cause adverse events. NSEs are considered a separate entity from adverse events, Dr. Benn said. According to her, in rare cases, live vaccines may induce the actual disease in some recipients, such as people born with gross defects in their immune systems or who have severe immunodeficiencies, such as fulminant AIDS. In the case of COVID-19 vaccines, live vaccines were likely not considered due to concerns about the formation of recombinant viruses when a vaccinated person comes into contact with the circulating viral strain. However, despite their potential beneficial NSEs, the COVID-19 vaccines may still be associated with adverse events because of the presence of highly toxic spike proteins, which studies now link to long COVID and vaccine injuries. In the medical textbook “The Immune Response,” the authors wrote that in isolated cases, live viral strains administered to individuals can regain virulence, causing disease in recipients. There’s also a risk of contamination with other viral strains during manufacturing. https://www.theepochtimes.com/health/vaccines-can-impact-long-term-survival-from-other-diseases-study-5559895

The Truth About HPV Vaccination, Part 3: Can It Prevent Cervical Cancer? There are no valid studies showing the vaccine for the human papillomavirus, or HPV, prevents cervical cancer. However, there are studies suggesting the vaccine could increase the risk of cancer. The Epoch Times Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. By Dr. Yuhong Dong Editor’s Note: This third installment in a multi-part series about the human papillomavirus, or HPV, vaccine examines studies that link the vaccines to increased risk of serious neurological and autoimmune disorders. Read Part 1 here and Part 2 here. In part 1 and part 2 of this series, we discussed the human papillomavirus (HPV) vaccine and its links to ovarian insufficiency and autoimmune disease. In part 3, we turn to questions regarding the effectiveness of the vaccine to prevent cervical cancer, and the limitations of relevant clinical trials to detect such a type of effect. Summary of key facts There are multiple obstacles in designing a valid clinical trial to prove the HPV vaccine could prevent cervical cancer, e.g. long lead time, lack of adequate informed consent, complexity between HPV infection and cervical cancer and the negative impact of girls’ sexual behavior, which may worsen the risks of cervical cancer. Most of the HPV’s interventional clinical trials have too short a follow-up time to draw a concrete conclusion. In a large Swedish observational trial, which is treated as the most convincing study to prove the HPV vaccine’s effects on cervical cancer, a few confounding factors were not adequately balanced between the HPV vaccination group versus the unvaccinated group. The National Cancer Institute’s Surveillance, Epidemiology, and End Results Program (SEER) data and another U.S. study found the HPV vaccine has no effects in reducing cancer rates. Two other registry-based studies in Australia and the U.K. suggest that HPV vaccination is associated with increased cervical cancer rates in certain age groups. Long lead time from HPV infection to cervical cancer Typically, there is a long period from HPV infection to cervical epithelium abnormalities, then cervical cancer. HPV infections usually last 12–18 months and are eventually cleared by the immune system. Fewer than 10% of HPV infections are persistent. There are two types of precancerous cervical lesions, low-grade or high-grade. Low-grade cervical neoplasia grade 1 (CIN1) is usually transient and resolves naturally within one to two years. Only a few persistent infections progress to the clinically meaningful high-grade, CIN2 or 3. Meanwhile, the median time from CIN2/3 to transition to cancer is estimated to be 23.5 years. Among those with weakened immune systems, HPV-related cancer might progress more quickly. In a review of the natural history of HPV infection, the complex pathway from infection to cancer is elucidated, including what is known (purple boxes) and where uncertainty remains (blue boxes). Difficulty running clinical trials for the HPV vaccine Because of the long lead time from HPV infection to cervical cancer, a prospective, randomized controlled trial is not easily designed and feasibly implemented. Lack of long-term follow-up is a common issue for most clinical trials to prove the HPV vaccine’s effectiveness in preventing cervical cancer. For example, a 2007 study found that Gardasil was effective in reducing HPV-associated cervical precancerous lesions rate by 20%. This study followed their subjects for only an average of three years after administration of the first dose. Furthermore, due to the complex uncertainties in the natural history between HPV infection and cervical cancer, it is not easy to claim the effectiveness of the HPV vaccine. A randomized trial is designed to balance the two groups — vaccine and placebo — so that any unmeasured confounding variables which might influence the outcome of the trial are distributed evenly. However, if the treatment group knows they got the vaccine, might their behaviors change? Might they be less risk-averse, thinking they have some protection? For example, girls might think they are vaccinated and “protected” from cervical cancer and may tend to initiate sexual intercourse at a younger age or engage in sexual activities with more partners. However, sexual intercourse at a young age, multiple sexual partners and oral contraceptive use are associated with an increased risk of cervical cancer in women. In other words, HPV vaccination may offer some protection if offered before sexual activity is initiated, but it may also be associated with increased behavioral risk factors. Whether the benefits of vaccination outweigh any risks is therefore a multifactorial question deserving of careful longitudinal study. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now Systemic analysis of 12 clinical trials on HPV vaccine efficacy In 2020, a Queen Mary University study led by Dr. Claire Rees reviewed 12 randomized clinical trials for Cervarix and Gardasil. The investigators found that the trials did not include populations representative of the vaccination target groups, and the trial design may have overstated vaccine efficacy. For example, one trial design generated evidence that the vaccine prevents CIN1. But this is not meaningful because these lesions usually resolve on their own. Furthermore, the study accessed efficacy against low-grade precancerous lesions. But this is not necessarily suggestive of efficacy against the more serious but much less frequent high-grade lesions. Finally, the cytology screenings were done every six to 12 months instead of every 36 months (normal screening interval), meaning the efficacy of the vaccine may have been overestimated, as low-grade lesions could go away spontaneously. All this is to say the HPV vaccine may be effective at preventing more serious lesions which lead to cervical cancer, but it is hard to know because of these poorly designed trials. Nothing is conclusive without a larger trial powered to detect a difference in rates of more serious cervical changes according to the typical screening schedule. However, such a trial has not yet been performed. Swedish nationwide health registry study A nationwide Swedish health registry-based study followed 1,672,983 women for 12 years to assess the association between HPV vaccination and the risk of cervical cancer. In this study, the cumulative incidence of cervical cancer was 47 cases per 100,000 women vaccinated and 94 per 100,000 unvaccinated, suggesting that HPV4 vaccination was associated with a reduced risk of 49 to 63% of invasive cervical cancer at the population level. Even though the results are positive, the study researchers raised a few concerns themselves. First, HPV-vaccinated women could have been generally healthier than unvaccinated women. This is known as “healthy volunteer bias.” Second, a mother’s history of cervical cancer might be associated with both vaccination uptake and underlying risk of cervical cancer as well as screening rates. Third, lifestyle and health factors such as smoking, sexual intercourse at a young age, multiple sexual partners, oral contraceptive use and obesity are reportedly associated with the risk of cervical cancer. These factors have not been thoroughly analyzed by this study and could have contributed to the data. Furthermore, parental education level and annual household income level may be interconnected with lifestyle factors such as smoking status. Strengths of this study include its size, duration and outcome of interest being invasive cancer, not low-grade lesions. However, it is impossible to exclude the relationship between lifestyle factors, vaccination uptake and cervical cancer. Only a randomized controlled trial (RCT) could balance the two groups on these unmeasured — but related — risk factors. However even if the risk factors (sexual behaviors) are fully balanced at baseline with an RCT, it is hard to keep them still balanced during the whole study course after HPV vaccination. No association found in a U.S. database Meanwhile, researchers found no association between vaccination and cancer mortality in the U.S. According to the National Cancer Institute’s SEER program, the incidence of deaths from cervical cancer before Gardasil’s introduction in the U.S. had been steadily declining for years and, in 2006, was 2.4 per 100,000 women. The data from 2016–2020 is 2.2 per 100,000 women — essentially unchanged. In a cross-sectional study using a nationally representative sample of U.S. adults aged 20–59 years, among 9,891 participants, the researchers did not find an association between HPV vaccination and HPV-related cancers. Increase in cervical cancer after HPV vaccine rollout: Australia In Australia, government data similarly reveal an increase in cervical cancer rates in certain age groups of women following the implementation of the Gardasil vaccine. Thirteen years after Gardasil was recommended for teenagers and young adults, there has been a 30% increase in 30- to 34-year-old women (4.9 cases/100,000 compared to 6.6 cases/100,000 in 2020) being diagnosed with cervical cancer. Even though the rates decreased in other age groups, the abnormal increase in the 30–34 age group needs an explanation. Several factors should be considered. First, this database does not tell the stage of cancer. More cancer diagnosed at an early stage may result in a cancer-rate increase. Second, decreasing cancer rates could be caused by declines in screening rates, perhaps due to the pandemic and/or a reluctance to get tested. Third, Australia has an increasing proportion of immigrants from South Asia, and these cultural factors may influence the cervical cancer-screening rate. A study of South Asian women living in Australia found that almost half had never had a previous screening test. Cervical cancer rates rise after HPV vaccination in the UK In the U.K., HPV vaccination was introduced in 2008 for girls aged 12–13 with catch-up for those aged 14–18. Many expected cervical cancer rates in women aged 20–24 to fall by 2014 as the vaccinated cohorts entered their 20s. However, in 2016 national statistics showed a worrying and substantial 70% increase in the rate of cervical cancer at ages 20 to 24 (i.e. from 2.7 in 2012 to 4.6 per 100,000 in 2014). While the author would consider it to be too early to draw conclusions regarding vaccine efficacy in protecting against cancer, this merits further study. Accordingly, an analysis was conducted in the U.K. in 2018 in response to public interest regarding this increase in cervical cancer. Researchers from Queen Mary University and King’s College London found that it was attributable to an increase in the proportion of women first screened at age 24.5 years. The increase was limited to stage I cervical cancer. But there was no evidence of a lack of screening leading to increasing rates. While the researchers considered it too early to conclude vaccine efficacy in protecting against cancer, these findings merit further study. Could HPV vaccines make HPV infections worse? Besides the vaccine’s unclear effectiveness in cancer prevention, studies further suggest the suppression of the HPV strains targeted by the vaccine may induce more virulent strains. For example, a 2015 study found that vaccinated young adult women had a higher prevalence of high-risk HPV types other than types 16 and 18, putting them at risk for more aggressive cervical and other HPV-related cancers. Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases in China, is the chief scientific officer and co-founder of a Swiss biotech company and former senior medical scientific expert for antiviral drug development at Novartis Pharma in Switzerland. If you or your child suffered harm after receiving the Gardasil HPV vaccine, you may have a legal claim. Please visit Wisner Baum for a free case evaluation. Click here to watch a Gardasil litigation update interview with Wisner Baum Senior Partner Bijan Esfandiari. https://childrenshealthdefense.org/defender/truth-hpv-vaccine-part-3-et/ https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-3.html

The Truth About HPV Vaccination, Part 1: How Safe Is It, Really? This first installment in a multi-part series about the human papillomavirus, or HPV, vaccine explores peer-reviewed scientific literature that reveals serious safety concerns about a vaccine widely regarded as safe. The Epoch Times Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. By Yuhong Dong The decline of public trust in COVID-19 vaccines significantly impacts vaccination rates against routine childhood diseases. This multiple-part series explores the international research done over the past two decades on the human papillomavirus (HPV) vaccine — believed to be one of the most effective vaccines developed to date. Summary of Key Facts This multiple-part series offers a thorough analysis of concerns raised about HPV vaccination following the global HPV campaign, which commenced in 2006. In the U.S., the HPV vaccine was reported to have a disproportionately higher percentage of adverse events of fainting and blood clots in the veins. The U.S. Food and Drug Administration (FDA) acknowledges that fainting can happen following the HPV vaccine, and recommends sitting or lying down to get the shot, then waiting for 15 minutes afterward. International scientists found that the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) logged a substantial increase in reports of premature ovarian failure from 1.4 per year before 2006 to 22.2 per year after the HPV vaccine approval, yielding a Proportional Reporting Ratio of 46.1. The HPV vaccine is widely regarded as one of the most effective vaccines developed to date. Nevertheless, safety issues have been raised following its approval, and in response, additional research has been published and litigation has been brought on behalf of those with a vaccine injury. In this HPV vaccine series, Parts I and II explain how the vaccine works and the evidence suggesting there may be legitimate safety concerns. The remaining parts present questions about real-world vaccine effectiveness and identify specific ingredients which may pose harm. The information presented here is drawn from peer-reviewed scientific literature from the U.S., Australia, Denmark, Sweden, France and Japan, as well as statistics published by public health agencies in each of these countries. More than 100 hours of research and internal peer review among scientists with experience in infectious diseases, virology, clinical trials and vaccine epidemiology have been invested in presenting this summary of the evidence. Large registry-based studies have identified plausible associations between HPV vaccination and autoimmune conditions, including premature ovarian insufficiency or premature ovarian failure, Guillain-Barré syndrome (GBS), postural orthostatic tachycardia syndrome and chronic regional pain syndrome. While it is easy to be enthusiastic about recent advances in human vaccine technology, we should keep in mind that achieving real and lasting good health is much more than just the absence of a certain virus. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now What is HPV? According to the CDC, HPV is the most common sexually transmitted infection in the U.S. HPV is a small DNA virus infecting human cutaneous epithelial cells in the mucosa and skin. More than 150 strains of the HPV virus have been identified. HPV infection is so common that the majority of sexually active people will get it at some point in their lives, even if they have only one or very few sexual partners. It can spread through sexual intercourse and oral sex. It can also pass between people through skin-to-skin contact, even by people who have no symptoms. HPV infection causes genital warts, some of which can turn into cancer. For the most part, however, HPV infection is benign. More than 90% of HPV infections cause no clinical symptoms and are self-limited, meaning the virus is cleared by the body via natural immunological defenses. HPV-associated cancers High-risk HPV types (types 16, 18 and others) can cause cervical cell abnormalities that are precursors to cancers. Type 16 is associated with approximately 50% of cervical cancers worldwide, and types 16 and 18 together are linked to 66% of cervical cancers. An additional five high-risk types, 31, 33, 45, 52 and 58, are linked with another 15% of cervical cancers and 11% of all HPV-associated cancers. Infection with a high-risk HPV type is associated with a higher chance of the development of cervical cancer but, by itself, HPV infection is not the sole risk factor to cause cancer. There are many other reasons, as discussed in this paper. Given the prevalence of infection, it is unsurprising that globally, cervical cancer is the fourth most common cancer in women. In 2018, an estimated 570,000 women were diagnosed with cervical cancer worldwide and more than 300,000 died of the disease. In the U.S., nearly 50,000 new HPV-associated cancers occur annually, with women infected at a slightly higher rate than men. But in 9 out of 10 cases, HPV goes away within two years without causing health problems. Only persistent HPV infections may lead to cancer. These infections evade the immune system’s innate cell-mediated defenses. The incidence of cervical cancer can be controlled as a result of the implementation of routine testing and screening, including Pap and DNA tests. HPV vaccines Three HPV vaccines — bivalent HPV vaccine (Cervarix, 2vHPV), quadrivalent HPV vaccine (Gardasil, 4vHPV or HPV4) and 9-valent HPV vaccine (Gardasil 9, 9vHPV) — have been licensed by the FDA. The HPV vaccine uses recombinant technology to assemble the shell of the virus — L1 capsid protein. These viral-like particles do not contain the virus genome and are not infectious. Cervarix, developed by GlaxoSmithKline, is a bivalent vaccine against HPV types 16 and 18, that was pulled from the U.S. market in 2016 due to “very low market demand.” Merck’s original Gardasil vaccine was designed to prevent infections from four strains (types 6, 11, 16 and 18). On June 8, 2006, after the FDA’s fast-tracked review, Gardasil was approved for use in females ages 9 to 26 for the prevention of cervical, vulvar and vaginal cancers. According to the label accompanying the vaccine, the ingredients in Merck’s first Gardasil vaccine were proteins of HPV, amorphous aluminum hydroxyphosphate sulfate, yeast protein, sodium chloride, L-histidine, polysorbate 80, sodium borate and water for injection. On Oct. 16, 2009, the FDA approved Gardasil (HPV4) for use in boys ages 9 through 26 for the prevention of genital warts caused by HPV types 6 and 11, but not for cancer. In 2010, it approved Gardasil for the prevention of anal cancer in males and females ages 9 to 26. Four years later, the FDA approved an updated vaccine, Merck’s Gardasil 9, for use in girls ages 9 to 26 and boys ages 9 to 15 for the prevention of cervical, vaginal and anal cancers. Gardasil 9 contains the same ingredients as Gardasil, but offers protection against nine HPV strains, adding five additional types (HPV types 31, 33, 45, 52 and 58). The current HPV vaccination schedule recommended by the CDC is two doses for both boys and girls aged 11 or 12. However, it is approved for children as young as 9. The second dose is given 6 to 12 months after the first. For those aged 15 and above, a three-dose schedule is implemented at one- to two-month and six-month intervals, although antibody-level studies suggest that two doses are sufficient. The vaccine prompts the body to produce neutralizing antibodies against HPV. Antibody responses appear to peak seven months after the first dose (or one month after the third dose). The vaccine-induced antibody levels appear to be 10 to 100 times higher than those after natural infection. The high vaccine effectiveness (90 to 98%) against the fast-growing, abnormal cells which may cause precancerous lesions in people ages 16 to 26 suggested that the best timing for vaccination was to give it to patients before they became sexually active. HPV VAERS reports from 2 large countries U.S. HPV vaccine adverse events On Aug. 19, 2009, the Journal of the American Medical Association published an article authored by scientists from the FDA and CDC that reviewed the safety data for Gardasil for adverse events reported to VAERS between June 2006 through December 2008. During that time, there were 12,424 reports of adverse events. Of these, 772 (6.2%) were serious. VAERS is a passive surveillance system, which is subject to multiple limitations, including underreporting, unconfirmed diagnosis, lack of denominator data and no unbiased comparison groups. Nevertheless, it is a useful and important tool for detecting postmarket safety issues with vaccines. A disproportionately high percentage of Gardasil VAERS reports were of syncope (fainting) and venous thromboembolic events (blood clots in the veins) compared with other vaccines. There were 8.2 syncope events per 100,000 HPV doses and 0.2 venous thromboembolic events per 100,000 HPV doses reported, respectively. The Gardasil package insert includes a warning about fainting, fever, dizziness, nausea and headaches (page 1) and notes at least the following adverse reactions reported during postmarketing surveillance (section 6.2): Guillain-Barré syndrome, transverse myelitis, motor neuron disease, venous thromboembolic events, pancreatitis and autoimmune disorders. Australia HPV vaccines adverse events In 2007, Australia reported an annual adverse drug reaction rate of 7.3/100,000, the highest since 2003, representing an 85% increase from 2006. Per the analysis of the Adverse Drug Reactions System database by the Australian Department of Health and Aging, this increase was “almost entirely due to” reports following the national rollout of the three-dose HPV vaccination program for young females in April 2007; 705 of the 1,538 adverse drug reactions reported that year were from the Gardasil vaccine. 1 vaccine adverse events australia chart In Australia, the ADR increase in 2007 was almost entirely due to the three-dose HPV vaccination program for females aged 12 to 26 years in April 2007. Credit: Australian Government Department of Health and Aged Care. Moreover, though people may take different vaccines other than HPV, the HPV vaccine was the only suspected vaccine to cause adverse reactions in 96% of records. Twenty-nine percent had causality ratings of “certain” or “probable” and 6% were defined as “serious.” 2 vaccine types vaccine suspected chart In these HPV-induced ADRs, 674 were suspected to be related to HPV vaccines, 203 had causality ratings of “certain” or “probable,” and 43 were defined as “serious.” Credit: Australian Government Department of Health and Aged Care. Japan withdraws recommendation, vaccine acceptance plunged In 2013, the Japanese raised concerns about a variety of widely reported post-vaccination serious adverse events. This led the government to suspend recommending the HPV vaccine for six years. Vaccine acceptance of HPV in Japan plunged significantly after 2013, from 42.9% to 14.3%, or from 65.4% to 3.9%. Researchers around the world also started to investigate HPV safety. A World Health Organization (WHO) position paper released on July 14, 2017, concluded that the HPV vaccines were “extremely safe.” The same report estimated approximately 1.7 cases of anaphylaxis per million HPV doses, that no association with GBS was found, and that syncope (fainting) was “established as a common anxiety or stress-related reaction to the injection.” In the spring of 2022, Japan announced it was relaunching its HPV vaccination drive. Mainstream news outlets reported that for thousands of women, the cost of caution may have led to preventable HPV-induced cancers and an estimated 5,000 to 5,700 deaths. However, a true risk-benefit analysis would also consider the number of serious adverse events prevented by putting the program on hold. The question remains: Was Japan’s caution warranted, or should their national vaccination program have continued? Ovarian insufficiency Concerns that the vaccine may be negatively affecting fertility have been detailed in the scientific literature. In 2014, a peer-reviewed case series describing premature ovarian failure among Australian women following HPV vaccination was published in the Journal of Investigative Medicine. This prompted other researchers to systematically examine the VAERS data to see if there was a connection between premature ovarian failure and Gardasil. Their study found a “potential safety signal” and concluded that “further investigations are warranted.” VAERS analysis on ovarian failure Two recent publications based on VAERS reports (first study, second study) found that events with a probable autoimmune background were significantly more frequent after HPV vaccination compared to other vaccinations. The team of international scientists that did the second study evaluated reports between 1990 and 2018. They found that among the 228,341 premature ovarian failure reports, 0.1% was considered to be associated with HPV vaccination with a median age of 15 years and the time to onset was 20.5 days following vaccination. The primary symptoms were amenorrhea (80.4%) and premature menopause (15.3%). Most strikingly, the mean number of premature ovarian failure cases increased significantly from 1.4 per year prior to 2006 to 22.2 per year after the HPV vaccine was approved, with a proportional reporting ratio of 46. The investigators noted that the WHO and CDC declared the HPV vaccine safe regardless of lacking adequate research into safety concerns. For example, the authors note that in a CDC-sponsored VAERS study, 17 cases of premature ovarian failure were identified but 15 were excluded due to insufficient information to confirm the diagnosis. A separate observational study using the Vaccine Safety Datalink found no increased risk. But this study was too underpowered to detect a signal. In addition, a cross-sectional survey study using National Health and Nutrition Examination Survey data relied on an inaccurate measurement of premature ovarian failure and self-reported HPV vaccination. In summary, the researchers detected a strong safety signal even after accounting for a potential upswing in reports due to media coverage after the product launch (they refer to this as “notoriety bias”). Because VAERS is a passive reporting system, the data may be incomplete and are often unconfirmed by physicians. Therefore, this study cannot provide a definitive link between HPV vaccination and premature ovarian insufficiency or premature ovarian failure but does generate a hypothetical link. The authors of the second study conclude by insisting that “this signal warrants well-designed and appropriate epidemiological research.” They note that “if the signal is confirmed, the risk is small compared to the lifetime risk of cervical cancer.” However, the benefit-risk profile on an individual level is not uniform. Given the health impacts of premature ovarian insufficiency and premature ovarian failure — some of which may be irreversible — and the declining mortality rate for cervical cancer even in the prevaccine era, the risk-benefit profile for HPV vaccination remains unclear. 3 case reports on ovarian insufficiency In the 2014 investigation mentioned above, a general practitioner in Australia noticed that three girls developed premature ovarian insufficiency following HPV4 vaccination. As a result of vaccination, each of the girls (ages 16, 16 and 18) had been prescribed oral contraception to treat menstrual cycle irregularities. Typically, women present with amenorrhea (no periods) or oligomenorrhea (infrequent periods) as the initial symptom of premature ovarian insufficiency. One girl had irregular periods following three doses of HPV vaccination. She then became amenorrheic and was diagnosed with premature ovarian insufficiency. Another girl’s periods were “like clockwork” until after the third HPV dose, which she received at age 15. Her first cycle after being vaccinated for the third time started two weeks late, and her next cycle was two months late. The final cycle began nine months later. The patient had no family history of early menopause. She was diagnosed with premature ovarian failure at 16. Lab work found hormone levels consistent with those of postmenopausal women, but her bone mineral density was normal. The authors of this case series noted that in preclinical studies of HPV4, the five-week-old rats only conceived one litter and the only available toxicology studies appear to be on the male rodent reproductive system. However, only two of three doses were administered prior to mating, and the overall fecundity was 95%, slightly lower than the control rats (98%) that received no vaccination prior to mating. The dose tolerance recommendations were based on an average weight of 50 kilograms for an adolescent girl but failed to take into account that HPV4 is administered to girls ages 9 to 13 years, who range in weight from 28 to 46 kilograms. Danish retrospective cohort study finds no link A 2021 study also evaluated premature ovarian insufficiency in a nationwide cohort of nearly 1 million Danish females ages 11 to 34 years. The researchers used Cox proportional hazard regression to detect an increased risk of premature ovarian insufficiency diagnosis by HPV4 vaccination status during the years 2007-2016. The hazard ratio for premature ovarian insufficiency (vaccinated versus unvaccinated) was 0.96. One limitation was that data on age at menarche (first menstruation) and oral contraceptive use were not available. Girls who had not yet reached menarche would not be at risk for premature ovarian insufficiency, of course. The authors excluded girls under age 15 in a sensitivity analysis and still found no signal, concluding that no association was found between HPV4 vaccination and premature ovarian insufficiency. Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases from China, is the chief scientific officer and co-founder of a Swiss biotech company and a former senior medical scientific expert for antiviral drug development at Novartis Pharma in Switzerland. If you or your child suffered harm after receiving the Gardasil HPV vaccine, you may have a legal claim. Please visit Wisner Baum for a free case evaluation. Click here to watch a Gardasil litigation update interview with Wisner Baum Senior Partner Bijan Esfandiari. The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children's Health Defense. https://childrenshealthdefense.org/defender/hpv-vaccine-safety-concerns-part-1-et/ https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-1.html

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Terrifying! New LETHAL BIO-WEAPON SARS-COV-3 Built and Hid by CHINA’s ARMY | VT Foreign Policy January 24, 2024 VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts Source: Embassy of Israel, Washington, D.C. and US Department of State. by Fabio Giuseppe Carlo Carisio VERSIONE IN ITALIANO The news is much more alarming than the mysterious and lethal Virus with which Bill Gates and his accomplices at the World Economic Forum have continued to threaten humanity for almost a year to push all governments to accept the Pandemic Treaty of the World Health Organization (financed by Bill & Melinda Gates Foundation), the international Vaccine Passport following the example of the European Union’s Green Pass and, consequently, a new wave of mandatory vaccinations to implement the global immunization plan launched by the Microsoft’s tycoon in 1999 in the Congress Center of Rockefeller in the Villa Serbelloni in Bellagio (Como). Perhaps it could be this new version of SARS-Cov-2, engineered in a laboratory at Being University and so powerful that it can be defined as SARS-Cov-3 due to its multiple mutations, the mysterious Disease X! Indeed after the investigation by Gospa News (published in Italian only), the study was modified, making the most alarming parts disappear… The suspicion comes from 4 disturbing circumstances that make the new, very dangerous Chinese research a real BIO-WEAPON capable of threatening all of humanity. It was developed with the help of military doctors of PLA: People’s Liberation Army of China. The laboratory experiments showed a lethality of 100% on humanized mice The research was carried out based on previous virological tests conducted by zoologist Shi Zhengli of the Wuhan Institute of Virology On January 21, 2024, the authors have modified the study by eliminating any terrifying reference to the 100% mortality on humanized mice, two days after the publication of the Gospa News investigation! Fortunately we have preserved both the screenshots and the original PDF study… A first study was published on December 18, 2022 in the specialized journal Emerging Microbes & Infections and on the same date also on PubMed, the library of the National Institute for Health (NIH) of the US Department of Health, but only in the update of a few days ago the lethality of the laboratory genotype of SARS-Cov-2 called GX_P2V was made known when the new research was relaunched the first time on January 4th in pre-print by BioRxivwhere it has yet to be subjected to peer review. The Abstract of the research up to January 21st was as brief as it was chilling: «SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR) can cause 100% mortality in human ACE2-transgenic mice, potentially attributable to late-stage brain infection. This underscores a spillover risk of GX_P2V into humans and provides a unique model for understanding the pathogenic mechanisms of SARS-CoV-2-related viruses». The study published on January 4th from which the role of a military doctor from the Beijing General Hospital of the PLA army can be deduced and, alongside, the study modified on January 21st with a new title and a new Abstract from which the alarm about 100% lethality in humanized mice disappeared The updated study instead appears with a new, less alarming title “An infection and pathogenesis mouse model of SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR)” has also been sweetened in the ABSTRACT from which any reference to the VERY HIGH LETHALITY of the virus created in the laboratory DISAPPEARS: «SARS-CoV-2-related pangolin coronavirus GX_P2V(short_3UTR) is highly attenuated, but can cause mortality in a specifically designed human ACE2-transgenic mouse model, making it an invaluable surrogate model for evaluating the efficacy of drugs and vaccines against SARS-CoV-2». Even more so after this SELF-CENSORSHIP, the previous original document that we wrote about takes on importance and on which we believe it is our duty to focus even if the researchers will obviously be able to claim that they are wrong… The study by Lai Wei et al. was conducted by Beijing Advanced Innovation Center for Soft Matter Science and Engineering, College of Life Science and Technology, Beijing University of Chemical Technology (China), with the collaboration of State Key Laboratory of Pharmaceutical Biotechnology, Medical School, Nanjing University, but also with Research Center for Clinical Medicine, The Fifth Medical Center of PLA General Hospital, Beijing, where the military doctor Shengdong Luo, present in both studies, and his colleague Weiwei Chen work. The latter is one of the various military hospitals that have taken the place of civilian facilities since 2016 as confirmed by a photo of the inauguration found on the internet. One of Beijing’s civilian hospitals converted into a military facility in 2016 One of the most disturbing aspects of this research is the fact that it derives from the previous study published in 2022 which highlighted only research aimed at producing a vaccine. While this new in-depth study has in fact transformed the study into the typology products defined in the US as “Dual Use Research of Concern (DURC)”where the dual utility consists precisely in the use as a vaccine or as a bio-weapon. From the “Smoking Gun” of Artificial SARS-Cov-2 to Beijing’s New Bio-Weapon This new and very dangerous experiment brings us back to the studies on chimeric coronaviruses at the Wuhan Institute of Virology where the scientist Shi Zhengli infected SARS strains with HIV plasmids since 2004 thanks to the funding of the Episars project of the European Commission chaired by Romano Prodi to experiment with an artificial enhancement of the wild virus which culminated in the so-called “smoking gun” on the origin of SARS-Cov-2 of Covid 19. «When I first saw the furin cleavage site in the viral sequence (of SARS-Cov-2 – ed.), with its arginine codons, I told my wife that it was the smoking gun for the origin of the virus”. This is what Dr. David Baltimore, a renowned American virologist and co-discoverer of reverse transcriptase, stated in support of the thesis (now much more than a theory) of the artificial origin of the pandemic pathogen which, to summarize it in a simple way , attaches itself to human cells and becomes lethal precisely thanks to that criticality in furin. Proof of this laboratory alteration emerged from a 2016 study, which remained almost unknown until recently, which was financed by the virologist Antony Fauci (former director of the American National Institute of Allergy and Infectious Diseases – NIAID) and conducted by US scientists, Wuhan researchers and Chinese medical doctors as revealed by the dossier of the US Senate Health Committee which not only ascertained the high probability of the artificial origin of SARS-Cov-2 but highlighted the role of American researchers… It is now known that Fauci himself admitted before the American Congress that the theory of the virus built in the laboratory is not a conspiracy as he instead claimed in a study on natural origins published shortly after some Indian scientists from the Kusuma School of Biology in New Delhi discovered the anomalous HIV sequences and reported them in a paper published in ResearchGate. But “they were then forced to withdraw” according to the late biologist Luc Montagnier, who was the first to publish research on artificial origin together with his biomathematician friend Jean-Claude Perez whom Gospa News interviewed exclusively a few months ago. In our investigations of the Wuhan-Gates cycle (in homage to Bill Gates who financed the Wuhan projects through EcoHealthAliance) we highlighted how the collaboration between the US and China started on biological weapons by former presidents Bill Clinton and Jiang Zemin was fundamental to the Predict-2 project on chimeric coronavirus researches funded by the Obama-Biden administration. This is why we have embraced the thesis of the patent expert David E. Martin who supported something very serious: according to him, in fact, the SARS-Cov-2 built between China and the US (but probably with contributions also in Canada, the United Kingdom and Ukraine) was allegedly intentionally released by the United States of America. In fact, it has brought to light too many intrigues between the research of Moderna Big Pharma (also financed by Gates and Fauci) and the Pentagon’s military agency DARPA. So China (led by Xi Jinping disliked by the Shanghai Clan of Jiang Zemin’s political heirs and his son who strengthened the Wuhan Institute of Virology) would have suffered, for the second time after the SARS of 2003 also built in a laboratory according to Martin and Russian genomics experts, the dispersal of the virus likely occurred during the World Military Games in Wuhan in October 2019. This is why, as reported recently by the Wall Street Journal, on the basis of documents obtained from the United States Department of Health, Chinese researchers isolated and mapped the Covid-19 virus at the end of December 2019, at least two weeks before Beijing revealed the details of the deadly virus to the world. According to the US newspaper, a Chinese researcher in Beijing uploaded an almost complete sequence of the structure of Covid into a database managed by the American government on December 28, 2019, while China shared the sequence of the virus with the World Health Organization (WHO) only 11 January 2020. In light of these considerations, the new experimentation also conducted by Chinese military doctors takes on an even more disturbing plot. So much so as to fuel the suspicion that Beijing has built a deadly bio-weapon ready to be spread in a global bacteriological war should new Western-inspired pandemics appear. Chinese research for a new attenuated vaccine against Covid-19 Now that we have analyzed the historical and geopolitical context, let’s briefly summarize the peculiarities of the two different studies on SARS-CoV-2 GX_P2V, the one for the 2022 vaccine and the one for the 2023 bioweapon. The first research by Beijing University for a new anti-Covid vaccine – link at the bottom of the page «SARS-CoV-2 related coronaviruses (SARS-CoV-2r) from Guangdong and Guangxi pangolins have been implicated in the emergence of SARS-CoV-2 and future pandemics. We previously reported the culture of a SARS-CoV-2r GX_P2V from Guangxi pangolins. Here we report the GX_P2V isolate rapidly adapted to Vero cells by acquiring two genomic mutations: an alanine to valine substitution in the nucleoprotein and a 104-nucleotide deletion in the hypervariable region (HVR) of the 3′-terminus untranslated region (3′-UTR)». This is what we read in the Abstract on PubMed of December 2022 regarding the research by Shanshan Lu et al. entitled “Induction of significant neutralizing antibodies against SARS-CoV-2 by a highly attenuated pangolin coronavirus variant with a 104nt deletion at the 3′-UTR”. «We further report the characterization of the GX_P2V variant (renamed GX_P2V(short_3UTR)) in in vitro and in vivo infection models. In cultured Vero, BGM and Calu-3 cells, GX_P2V(short_3UTR) had similar robust replication kinetics, and consistently produced minimum cell damage. GX_P2V(short_3UTR) infected golden hamsters and BALB/c mice but was highly attenuated. Golden hamsters infected intranasally had a short duration of productive infection in pulmonary, not extrapulmonary, tissues». The Abstract then goes into the specifics of the development of an antidote against Covid based not on the new and controversial biotechnology of mRNA gene sera but on that of traditional vaccines: «These productive infections induced neutralizing antibodies against pseudoviruses of GX_P2V and SARS-CoV-2. Collectively, our data show that the GX_P2V(short_3UTR) is highly attenuated in in vitro and in vivo infection models. Attenuation of the variant is likely partially due to the 104-nt deletion in the HVR in the 3′-UTR. This study furthers our understanding of pangolin coronaviruses pathogenesis and provides novel insights for the design of live attenuated vaccines against SARS-CoV-2». The Army Laboratory Experiment for a Bacteriological Weapon The recently published study with the already extremely alarming title “Lethal Infection of Human ACE2- Transgenic Mice Caused by SARS-CoV-2-related Pangolin Coronavirus GX_P2V(short_3UTR)” had a different impact, before it was altered on January 21 to mitigate its hazard… This work was supported by NSFC-MFST project (China–Mongolia) (grant number 32161143027), National Key R&D Program of China (2021YFC2301804) and Biosafety Special Program (No. 19SWAQ 13). «Two SARS-CoV-2-related pangolin coronaviruses, GD/2019 and GX/2017, were identified prior to the COVID-19 outbreak (1,2). The respective isolates, termed pCoV-GD01 and GX_P2V, were cultured in 2020 and 2017, respectively (2,3). The infectivity and pathogenicity of these isolates have been studied (4–6). The pCoV-GD01 isolate, which has higher homology with SARS-CoV-2, can infect and cause disease in both golden hamsters and hACE2 mice (4)». We read in the pre-print research by Lai Wei et al.: «In contrast, while GX_P2V can also infect both species, it does not appear to cause obvious disease in these animals (5,6). We previously reported that the early passaged GX_P2V isolate was actually a cell culture-adapted mutant, named GX_P2V(short_3UTR), which possesses a 104-nucleotide deletion at the 3’-UTR (6). In this study, we cloned this mutant, considering the propensity of coronaviruses to undergo rapid adaptive mutation in cell culture, and assessed its pathogenicity in hACE2 mice. We found that the GX_P2V(short_3UTR) clone can infect hACE2 mice, with high viral loads detected in both lung and brain tissues. This infection resulted in 100% mortality in the hACE2 mice. We surmise that the cause of death may be linked to the occurrence of late brain infection». The cover of the study published on January 4 on BiorXiv before the modification on January 21, 2024 – link at the bottom of the page Then they also recall that these SARS-CoV-2, GD/2019 and GX/2017 studies were initially carried out by the well-known scientist from the Wuhan Institute of Virology: «To the best of our knowledge, this is the first report showing that a SARS-CoV-2-related pangolin coronavirus can cause 100% mortality in hACE2 mice, suggesting a risk for GX_P2V to spill over into humans. Our findings are evidently inconsistent with those of Zhengli Shiet al. (5), who tested the virulence of GX_P2V in two different hACE2 mouse models». The discussion then becomes very technical and evidence of expert biochemists or virologists: «It is important to note that we did not isolate the wild-type GX_P2V strain. The study by Zhengli Shi et al tested the GX_P2V(short_3UTR) variant that we reported. However, the adaptative evolutionary changes of this variant during their laboratory culture remain understudied. In fact, according to additional infection experiments, the uncloned GX_P2V(short_3UTR) also resulted in 100% mortality in hACE2 mice. Due to the propensity of coronaviruses to undergo adaptive mutation during passage culture, we cloned and analyzed mutations in GX_P2V(short_3UTR), focusing specifically on the pathogenicity of the cloned strains. The high pathogenicity mechanism of GX_P2V C7 in hACE2 mice, in the absence of the wild-type GX_P2V control, requires further investigation». And the conclusion doesn’t suggest anything good… «Compared to the original sequence of GX_P2V(short_3UTR), GX_P2V C7 has two amino acid mutations in the spike protein. Given the close relationship between coronavirus virulence and spike protein mutations (7), it is possible that GX_P2V C7 has undergone a virulence-enhancing mutation. However, it is important to note that our hACE2 mouse model may be relatively unique. The company has not yet published a paper on this hACE2 mouse model, but our results suggest that hACE2 may be highly expressed in the mouse brain. Additionally, according to the data provided by the company, these hACE2 mice have abnormal physiology, as indicated by relatively reduced serum triglyceride, cholesterol, and lipase levels, compared to those of wild-type C57BL/6J mice. In summary, our study provides a unique perspective on the pathogenicity of GX_P2V and offers a distinct alternative model for understanding the pathogenic mechanisms of SARS-CoV-2-related coronaviruses». The scientific explanation is cloaked by a strong emphasis on virulence which may also appear as a “threat” on the possibility of transforming these GX_P2V genotypes into a real bacteriological weapon. Fabio Giuseppe Carlo Carisio © COPYRIGHT GOSPA NEWS prohibition of reproduction without authorization follow Fabio Carisio Gospa News director on Twitter follow Gospa News on Telegram Subscribe to the Gospa News Newsletter to read the news as soon as it is published MAIN SOURCES PUBMED – Induction of significant neutralizing antibodies against SARS-CoV-2 by a highly attenuated pangolin coronavirus variant with a 104nt deletion at the 3′-UTR’ BIORXIV – Lethal Infection of Human ACE2-Transgenic Mice Caused by SARS-CoV-2-related Pangolin Coronavirus GX_P2V(short_3UTR) To receive the COMPLETE PDF OF THE ORIGINAL DISTURBING RESEARCH, subscribe to the Gospa News Newsletter and write to [email protected] GOSPA NEWS – WUHAN-GATES DOSSIER GOSPA NEWS – COVID-19 DOSSIER Fabio G. C. Carisio Fabio is investigative journalist since 1991. Now geopolitics, intelligence, military, SARS-Cov-2 manmade, NWO expert and Director-founder of Gospa News: a Christian Information Journal. His articles were published on many international media and website as SouthFront, Reseau International, Sputnik Italia, United Nation Association Westminster, Global Research, Kolozeg and more… Most popolar investigation on VT is: Rumsfeld Shady Heritage in Pandemic: GILEAD’s Intrigues with WHO & Wuhan Lab. Bio-Weapons’ Tests with CIA & Pentagon Fabio Giuseppe Carlo Carisio, born on 24/2/1967 in Borgosesia, started working as a reporter when he was only 19 years old in the alpine area of Valsesia, Piedmont, his birth region in Italy. After studying literature and history at the Catholic University of the Sacred Heart in Milan, he became director of the local newspaper Notizia Oggi Vercelli and specialized in judicial reporting. For about 15 years he is a correspondent from Northern Italy for the Italian newspapers Libero and Il Giornale, also writing important revelations on the Ustica massacre, a report on Freemasonry and organized crime. With independent investigations, he collaborates with Carabinieri and Guardia di Finanza in important investigations that conclude with the arrest of Camorra entrepreneurs or corrupt politicians. In July 2018 he found the counter-information web media Gospa News focused on geopolitics, terrorism, Middle East, and military intelligence. In 2020 published the book, in Italian only, WUHAN-GATES – The New World Order Plot on SARS-Cov-2 manmade focused on the cycle of investigations Wuhan-Gates His investigations was quoted also by The Gateway Pundit, Tasnim and others He worked for many years for the magazine Art & Wine as an art critic and curator. VETERANS TODAY OLD POSTS www.gospanews.net/ ATTENTION READERS We See The World From All Sides and Want YOU To Be Fully Informed In fact, intentional disinformation is a disgraceful scourge in media today. So to assuage any possible errant incorrect information posted herein, we strongly encourage you to seek corroboration from other non-VT sources before forming an educated opinion. About VT - Policies & Disclosures - Comment Policy Due to the nature of uncensored content posted by VT's fully independent international writers, VT cannot guarantee absolute validity. All content is owned by the author exclusively. Expressed opinions are NOT necessarily the views of VT, other authors, affiliates, advertisers, sponsors, partners, or technicians. Some content may be satirical in nature. All images are the full responsibility of the article author and NOT VT. https://www.vtforeignpolicy.com/2024/01/terrifying-new-lethal-bio-weapon-sars-cov-3-built-and-hid-by-chinas-army/

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

Who Wants The Next Pandemic And Why? Who Wants The Next Pandemic And Why? #COVID-19#RUSSIA 16.01.2024 - 1789 views 8 1 0 Share1 12 Support SouthFrontPDF Download Who Wants The Next Pandemic And Why? Click to see the full-size image Written by Drago Bosnic, independent geopolitical and military analyst It’s been nearly two years since Russia uncovered the extremely disturbing truth about American involvement in bioweapons testing in Ukraine. However, the institutions of the so-called “rules-based world order” (posing as the “international community”) have completely ignored these findings, while the mainstream propaganda machine has done everything in its power to present them as supposed “conspiracy theories”. Still, the world has been demanding answers from the US-led political West. This includes non-aligned countries, often dubbed the “fence sitters” by the United States, although there have been far worse descriptions used by the European Union. American diplomacy (if one could even call it that way) is too busy meddling in the internal affairs of other countries, so it usually refuses to comment on allegations regarding the Pentagon-run “biological research facilities” in Ukraine. Luckily for the world, the Russian military never stopped investigating this issue, despite constant attempts to prevent, sabotage and/or discredit these efforts. On January 15, TASS reported that the Russian Ministry of Defense (MoD) identified over 50 participants in America’s bioweapons program in Ukraine last year alone. During a briefing held on the same day, Lieutenant General Igor Kirillov, Head of the Russian Armed Forces’ Nuclear, Biological and Chemical (NBC) Protection Troops, warned about the dangers of these US-sponsored illicit activities. Kirillov revealed that an event that can only be described as a false flag training exercise was held in Lvov back in August 2023. The goal was to accuse Russia of supposed bioweapons usage in Ukraine, likely as a way for the US/NATO to both incriminate Moscow and divert attention away from itself and its illegal biological warfare activities in the war-torn country. “I would like to note the work carried out in 2023 to identify the organizers and participants of military-biological activities on the territory of Ukraine. As a result of the analysis of the documentation obtained, more than 50 people were identified, including officials of US and Ukrainian government agencies, and employees of intermediary organizations and private companies,” Kirillov said at the briefing. Among others, he named Kenneth Myers, Robert Pope and Joanna Wintrol, employees of the US DoD’s Cooperative Threat Reduction Program, as well as representatives of the companies Battelle and EcoHealth Alliance, Kevin Olival, Karen Saylors and Lewis von Thaer. “The [false flag] event [in Lvov] was attended by Filippa Lentzos; Gemma Bowsher; and Irina Demchyshyna, Head of the Reference Laboratories of the Public Health Center of the Ukrainian Health Ministry; as well as Darya Ponomarenko, Head of the Department of Biological Safety and Biological Protection of the Public Health Center of the Ukrainian Health Ministry,” Kirillov said. He added that R&D on pathogens that could cause massive economic damage was extensively conducted in these biolabs, including research on mechanisms for their more efficient distribution and spreading. The program was conducted under the leadership of Denis Muziyka. In addition, Viktor Gavrilenko and Alexander Mezinov were involved in the collection and shipment of materials. It can be argued the report essentially shows that the endgame was to cause long-term damage to the Russian economy (particularly its massive agricultural potential). In turn, this was supposed to cause instability in the country, possibly even a famine that could destabilize the Russian government. Needless to say, such activities are tantamount to a declaration of war. And yet, those conducting them are completely unmoved by the possibility of a direct confrontation between nuclear-armed superpowers. In further reports published later that day, TASS revealed additional goals of these US-run biolabs. General Kirillov touched upon the US strategy of (ab)using its publicly stated goals of supposedly “monitoring infectious diseases and providing assistance to developing countries” to further expand its biological warfare capabilities. “Over the past year, the Pentagon has developed and adopted a number of conceptual documents that involve expanding the foreign network of US-controlled biological laboratories and continuing military biological research beyond national jurisdiction. <…> While the stated goals are monitoring infectious diseases and providing assistance to developing countries, using the example of Ukraine, it became clear how the military-biological potential of the United States is being built up,” he stated. Kirillov also recalled that Washington DC created new administrative and technical agencies last year – the Office of Pandemic Preparedness and Response Policy, and the Bureau of Global Health Security and Diplomacy. These two agencies are supposed to serve as fronts for further bioweapons programs, not only in Ukraine, but around the world. Kirillov also reiterated previous findings uncovered after the start of the special military operation (SMO). He specifically mentioned the Pentagon’s two major projects in Ukraine, aimed at studying the causative agents of particularly dangerous pathogens and diseases such as tularemia, anthrax and hantavirus infections. “The research was carried out in three main areas. These are monitoring the biological situation, collecting endemic strains, and studying the susceptibility of the local population,” Kirillov said. In an additional report by the South Front, the Russian military revealed that the US Department of Defense conducted a series of experiments with smallpox viruses, which is prohibited by the World Health Assembly. This also includes research on the use of the monkeypox virus as a bioweapon, as well as R&D on the usage of agent-based simulators of smallpox viruses. Two strains of this pathogen are used in the course of aerobic studies. The World Health Assembly allows only two organizations to conduct such research – the Vector State Scientific Center in Russia and the Center for Disease Control in the US. However, these experiments were conducted by the employees of the Institute of Infectious Diseases, which is subordinate to the Pentagon. The US DoD was also engaged in studying other orthopoxviruses that are deadly and pose great danger to human life and health. Interestingly (or perhaps “terrifyingly” would be a much more fitting term), concurrently with the Russian military’s briefings, the infamous World Economic Forum announced it would discuss the new unspecified deadly pathogen that causes what they call the “Disease X”, which the WEF claims is “10 times deadlier than the COVID-19”. Considering the fact that the WEF is deeply intertwined with the political West and its vaunted “rules-based world order”, the timing is rather peculiar. Why are the WEF and the so-called “international community” so “worried” about an unknown disease, but they keep ignoring clear-cut evidence of America’s massive (and rapidly expanding) bioweapons program? Why is the US military conducting this sort of research (on a global scale, at that), although any official civilian public health institution could easily do so on its own and without such deadly biohazard risks? MORE ON THE TOPIC: US Military Conducts Dangerous Experiments With Prohibited Viruses Kiev Sold Ukrainian Land For Disposal Of Hazardous Chemical Waste Of US Companies – Report Moscow Accuses Washington Of Preparing For New Pandemic 8 1 0 Share1 12 Support SouthFrontPDF Download https://southfront.press/who-wants-the-next-pandemic-and-why/