• What’s going on with the #somee family?! Let’s be productive and post real content on some! I would love to be a part of your lifes. #happy #back #productive #motivation #positivechanges #believer
    What’s going on with the #somee family?! Let’s be productive and post real content on some! I would love to be a part of your lifes. #happy #back #productive #motivation #positivechanges #believer
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  • 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
    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
    BLOG.MYGOTODOC.COM
    So You Got Spiked: Now What?
    Especially important for athletes and future parents: invest in your health, your future & future generations.
    Like
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  • ‘Operation Al-Aqsa Flood’ Day 175: ICJ orders Israel to stop famine in Gaza as Israel continues to raid hospitals
    The International Court of Justice imposed new provisional measures in South Africa’s case against Israel for its genocide in Gaza, ordering Israel to ensure the entry of food and other supplies in order to stop the spreading famine.

    Qassam MuaddiMarch 29, 2024
    Two injured Palestinian children are being treated by doctors on the floor of a hospital in southern Gaza, following Israeli airstrikes.
    Injured Palestinian children are brought to Abu Youssef Al-Najjar Hospital in Rafah for treatment following Israeli attacks on the southern Gaza Strip,on March 29, 2024. (Ahmed Ibrahim/APA Images)
    Casualties

    32,623 + killed* and at least 75,092 wounded in the Gaza Strip.
    450+ Palestinians killed in the occupied West Bank and East Jerusalem.**
    Israel revises its estimated October 7 death toll down from 1,400 to 1,139.
    597 Israeli soldiers have been killed since October 7, and at least 3,221 injured.***
    *Gaza’s Ministry of Health confirmed this figure on its Telegram channel. Some rights groups estimate the death toll to be much higher when accounting for those presumed dead.

    ** The death toll in the West Bank and Jerusalem is not updated regularly. According to the PA’s Ministry of Health on March 17, this is the latest figure.

    *** This figure is released by the Israeli military, showing the soldiers whose names “were allowed to be published.”

    Advertisement

    Watch now: NOURA ERAKAT on Witnessing Palestine with Frank Barat
    Key Developments

    Israeli forces killed 71 Palestinians and wounded 112 in air and artillery strikes across the Gaza Strip.
    Israel’s raid into al-Shifa hospital enters its 12th day, destroying more buildings in the vicinity of the hospital.
    Israel releases 102 Palestinians detained from Gaza in recent weeks.
    Israel admits eight soldiers wounded in 24 hour period as fighting between Israeli army and Palestinian resistance intensifies in Gaza City and in Khan Younis.
    ICJ orders new provisional measures in South Africa’s genocide case against Srael, including provisions to prevent famine.
    North Gaza-based journalist Bayan Abu Sultan, who was feared missing since March 19 after reporting that Israeli forces killed her brother in front of her, reappears on Twitter and confirms that she is alive.
    At least 40 Syrian soldiers and Hezbollah fighters killed in Israeli strikes on Aleppo, Syria.
    UN special rapporteur for Palestine says, “there is enough grounds to believe that Israel is committing genocide.”
    West Bank: One Palestinian teenager was wounded in al-Fawwar refugee camp south of Hebron, in an Israeli raid.
    West Bank: Israel raids Nablus and the refugee camps of Shu’fat and Qalandia north of Jerusalem.
    71 Palestinians killed, death toll rises to 32,623

    The Palestinian health ministry announced in a statement on Thursday that 71 Palestinians were killed in Israeli strikes across the Gaza Strip, while 112 others were wounded in the past day.

    In Gaza City, the Israeli army continued its raid on al-Shifa Hospital for the 12th day. Local sources reported that Israeli forces burned and demolished several buildings in the surroundings of al-Shifa.

    Medical sources said that Israeli forces continue to hold 160 Palestinians, including medical staff, in the Human Development building in the al-Shifa complex.

    In Deir al-Balah, in the center Gaza Strip, Israeli warships opened fire at Palestinian homes on the beachfront. In Al-Maghazi refugee camp, east of Deir al-Balah, an Israeli strike on the Mousa family home killed six people, including both parents and four children, wounding several of their neighbors.

    In Khan Younis, Israeli strikes killed 12 Palestinians, while a nurse was reported killed by Israeli troops at the Nasser hospital.

    In Rafah, in southern Gaza, Israeli strikes on the east and center of the city killed at least 12 Palestinians, including children.

    Viral journalist reported missing reappears, Israel releases 102 Gaza detainees

    The Israeli army released 102 Palestinians who were detained from the Gaza Strip and held in Israeli custody for several days and weeks, according to local media reports.

    According to the Palestinian Red Crescent Society, nine of the released are paramedics who work for the society and who were detained for 46 days. Three of the released were taken to some of the few remaining operating hospitals in Gaza to be treated from the effects of torture, the group said.

    Meanwhile, Palestinian journalist Bayan Abu Sultan, who was reported missing in the surroundings of al-Shifa since March 19, posted on social media Thursday for the first time in 12 days.

    “I survived,” Bayan wrote on Thursday on X. Her last tweet before she disappeared read “Israeli forces killed my only brother in front of my eyes.”

    Bayan is one of the few Palestinian journalists still reporting from Gaza City and the north. She and her family were staying in the vicinity of al-Shifa Hospital, where her family returned after being displaced in the early weeks of the Israeli assault when her brother was killed.

    After activists and journalists began sounding the alarm over Bayan’s feared disappearance, Reporters Without Borders demanded in a statement that Israeli forces provide information about Bayan’s whereabouts, assuming that she was detained.

    Palestinians remaining in Gaza City continue to face severe shortages of supplies, especially of food. “Hunger, the shortage of goods and skyrocketing prices have made people [in Gaza City] lose taste for life,” Huda Amer, another Gaza-city-based journalist, told Mondoweiss. “We hear bombings and shootings in the street”, she added.

    UN rapporteur says ‘enough grounds’ for genocide in Gaza

    The United Nations Special Rapporteur on the Occupied Palestinian Territories, Francesca Albanese, said that there are “enough grounds” to believe that Israel is committing genocide against the Palestinian people in the Gaza Strip.

    Albanese made her remarks on Thursday during the presentation of her report entitled “Anatomy of a Genocide” to the UN Human Rights Council in Geneva.

    The report, which was released earlier this week, indicated that Israel was violating three of the five acts described in the Genocide Convention.

    Albanese said that she has received threats because of her report, and that she has been pressured and “attacked” since the beginning of her mandate.

    Commenting on Albanese’s report, the White House’s spokesperson Mathew Miller accused Albanese of “making antisemitic comments,” and that the entire post of human rights rapporteur for the occupied Palestinian Territories was “unproductive.” In February, Israel denied Albanese entry to the country.

    On Thursday, the International Court of Justice ordered a new set of provisional measures to prevent genocide, including provisions to prevent famine.

    The measures were requested by South Africa as part of its ongoing case against Israel at the international court.

    The ICJ judges noted that “Palestinians are no longer facing the risk of famine … but famine is setting in”. The court ordered Israel to ensure the “unhindered provision at scale by all concerned of urgently needed basic services and humanitarian assistance,” including food, water, fuel, and medical supplies. The order is legally binding, though, like the initial provisional measures granted by the court back in January, and since ignored by Israel, the court does not have an enforcement mechanism.

    Already, 31 Palestinians, mostly children, have died of food shortage in the Gaza Strip since Israel imposed a total blockade of food, water, electricity, and fuel on the 2 million people living there in the immediate aftermath of October 7.

    Israeli army wounds on Palestinian, raids West Bank towns

    A Palestinian man was wounded in the stomach by Israeli forces on Thursday night during an Israeli military raid on the al-Fawwar refugee camp, south of Hebron in the occupied West Bank.

    Local media sources reported that Israeli forces fired light flares before entering the camp, and that they were confronted by local youth throwing stones. Israeli troops responded with live fire, wounding one man.

    Israeli forces also raided Shu’fat and Qalandia, north of Jerusalem, and Nablus in the northern West Bank.

    Meanwhile, Israeli forces continue to impose tight control on checkpoints in the Jordan Valley as they continue to search for the gunman behind yesterday’s shooting at an Israeli settlers’ bus north of Jericho, which wounded three Israelis.

    Israel has arrested more than 7,800 Palestinians since October 7. Currently, at least 9,100 Palestinians are held in Israeli prisons, including 50 women, 200 children, and more than 3500 detainees without charges.

    BEFORE YOU GO – At Mondoweiss, we understand the power of telling Palestinian stories. For 17 years, we have pushed back when the mainstream media published lies or echoed politicians’ hateful rhetoric. Now, Palestinian voices are more important than ever.

    Our traffic has increased ten times since October 7, and we need your help to cover our increased expenses.

    Support our journalists with a donation today.

    https://mondoweiss.net/2024/03/operation-al-aqsa-flood-day-175-icj-orders-israel-to-stop-famine-in-gaza-as-israel-continues-to-raid-hospitals/
    ‘Operation Al-Aqsa Flood’ Day 175: ICJ orders Israel to stop famine in Gaza as Israel continues to raid hospitals The International Court of Justice imposed new provisional measures in South Africa’s case against Israel for its genocide in Gaza, ordering Israel to ensure the entry of food and other supplies in order to stop the spreading famine. Qassam MuaddiMarch 29, 2024 Two injured Palestinian children are being treated by doctors on the floor of a hospital in southern Gaza, following Israeli airstrikes. Injured Palestinian children are brought to Abu Youssef Al-Najjar Hospital in Rafah for treatment following Israeli attacks on the southern Gaza Strip,on March 29, 2024. (Ahmed Ibrahim/APA Images) Casualties 32,623 + killed* and at least 75,092 wounded in the Gaza Strip. 450+ Palestinians killed in the occupied West Bank and East Jerusalem.** Israel revises its estimated October 7 death toll down from 1,400 to 1,139. 597 Israeli soldiers have been killed since October 7, and at least 3,221 injured.*** *Gaza’s Ministry of Health confirmed this figure on its Telegram channel. Some rights groups estimate the death toll to be much higher when accounting for those presumed dead. ** The death toll in the West Bank and Jerusalem is not updated regularly. According to the PA’s Ministry of Health on March 17, this is the latest figure. *** This figure is released by the Israeli military, showing the soldiers whose names “were allowed to be published.” Advertisement Watch now: NOURA ERAKAT on Witnessing Palestine with Frank Barat Key Developments Israeli forces killed 71 Palestinians and wounded 112 in air and artillery strikes across the Gaza Strip. Israel’s raid into al-Shifa hospital enters its 12th day, destroying more buildings in the vicinity of the hospital. Israel releases 102 Palestinians detained from Gaza in recent weeks. Israel admits eight soldiers wounded in 24 hour period as fighting between Israeli army and Palestinian resistance intensifies in Gaza City and in Khan Younis. ICJ orders new provisional measures in South Africa’s genocide case against Srael, including provisions to prevent famine. North Gaza-based journalist Bayan Abu Sultan, who was feared missing since March 19 after reporting that Israeli forces killed her brother in front of her, reappears on Twitter and confirms that she is alive. At least 40 Syrian soldiers and Hezbollah fighters killed in Israeli strikes on Aleppo, Syria. UN special rapporteur for Palestine says, “there is enough grounds to believe that Israel is committing genocide.” West Bank: One Palestinian teenager was wounded in al-Fawwar refugee camp south of Hebron, in an Israeli raid. West Bank: Israel raids Nablus and the refugee camps of Shu’fat and Qalandia north of Jerusalem. 71 Palestinians killed, death toll rises to 32,623 The Palestinian health ministry announced in a statement on Thursday that 71 Palestinians were killed in Israeli strikes across the Gaza Strip, while 112 others were wounded in the past day. In Gaza City, the Israeli army continued its raid on al-Shifa Hospital for the 12th day. Local sources reported that Israeli forces burned and demolished several buildings in the surroundings of al-Shifa. Medical sources said that Israeli forces continue to hold 160 Palestinians, including medical staff, in the Human Development building in the al-Shifa complex. In Deir al-Balah, in the center Gaza Strip, Israeli warships opened fire at Palestinian homes on the beachfront. In Al-Maghazi refugee camp, east of Deir al-Balah, an Israeli strike on the Mousa family home killed six people, including both parents and four children, wounding several of their neighbors. In Khan Younis, Israeli strikes killed 12 Palestinians, while a nurse was reported killed by Israeli troops at the Nasser hospital. In Rafah, in southern Gaza, Israeli strikes on the east and center of the city killed at least 12 Palestinians, including children. Viral journalist reported missing reappears, Israel releases 102 Gaza detainees The Israeli army released 102 Palestinians who were detained from the Gaza Strip and held in Israeli custody for several days and weeks, according to local media reports. According to the Palestinian Red Crescent Society, nine of the released are paramedics who work for the society and who were detained for 46 days. Three of the released were taken to some of the few remaining operating hospitals in Gaza to be treated from the effects of torture, the group said. Meanwhile, Palestinian journalist Bayan Abu Sultan, who was reported missing in the surroundings of al-Shifa since March 19, posted on social media Thursday for the first time in 12 days. “I survived,” Bayan wrote on Thursday on X. Her last tweet before she disappeared read “Israeli forces killed my only brother in front of my eyes.” Bayan is one of the few Palestinian journalists still reporting from Gaza City and the north. She and her family were staying in the vicinity of al-Shifa Hospital, where her family returned after being displaced in the early weeks of the Israeli assault when her brother was killed. After activists and journalists began sounding the alarm over Bayan’s feared disappearance, Reporters Without Borders demanded in a statement that Israeli forces provide information about Bayan’s whereabouts, assuming that she was detained. Palestinians remaining in Gaza City continue to face severe shortages of supplies, especially of food. “Hunger, the shortage of goods and skyrocketing prices have made people [in Gaza City] lose taste for life,” Huda Amer, another Gaza-city-based journalist, told Mondoweiss. “We hear bombings and shootings in the street”, she added. UN rapporteur says ‘enough grounds’ for genocide in Gaza The United Nations Special Rapporteur on the Occupied Palestinian Territories, Francesca Albanese, said that there are “enough grounds” to believe that Israel is committing genocide against the Palestinian people in the Gaza Strip. Albanese made her remarks on Thursday during the presentation of her report entitled “Anatomy of a Genocide” to the UN Human Rights Council in Geneva. The report, which was released earlier this week, indicated that Israel was violating three of the five acts described in the Genocide Convention. Albanese said that she has received threats because of her report, and that she has been pressured and “attacked” since the beginning of her mandate. Commenting on Albanese’s report, the White House’s spokesperson Mathew Miller accused Albanese of “making antisemitic comments,” and that the entire post of human rights rapporteur for the occupied Palestinian Territories was “unproductive.” In February, Israel denied Albanese entry to the country. On Thursday, the International Court of Justice ordered a new set of provisional measures to prevent genocide, including provisions to prevent famine. The measures were requested by South Africa as part of its ongoing case against Israel at the international court. The ICJ judges noted that “Palestinians are no longer facing the risk of famine … but famine is setting in”. The court ordered Israel to ensure the “unhindered provision at scale by all concerned of urgently needed basic services and humanitarian assistance,” including food, water, fuel, and medical supplies. The order is legally binding, though, like the initial provisional measures granted by the court back in January, and since ignored by Israel, the court does not have an enforcement mechanism. Already, 31 Palestinians, mostly children, have died of food shortage in the Gaza Strip since Israel imposed a total blockade of food, water, electricity, and fuel on the 2 million people living there in the immediate aftermath of October 7. Israeli army wounds on Palestinian, raids West Bank towns A Palestinian man was wounded in the stomach by Israeli forces on Thursday night during an Israeli military raid on the al-Fawwar refugee camp, south of Hebron in the occupied West Bank. Local media sources reported that Israeli forces fired light flares before entering the camp, and that they were confronted by local youth throwing stones. Israeli troops responded with live fire, wounding one man. Israeli forces also raided Shu’fat and Qalandia, north of Jerusalem, and Nablus in the northern West Bank. Meanwhile, Israeli forces continue to impose tight control on checkpoints in the Jordan Valley as they continue to search for the gunman behind yesterday’s shooting at an Israeli settlers’ bus north of Jericho, which wounded three Israelis. Israel has arrested more than 7,800 Palestinians since October 7. Currently, at least 9,100 Palestinians are held in Israeli prisons, including 50 women, 200 children, and more than 3500 detainees without charges. BEFORE YOU GO – At Mondoweiss, we understand the power of telling Palestinian stories. For 17 years, we have pushed back when the mainstream media published lies or echoed politicians’ hateful rhetoric. Now, Palestinian voices are more important than ever. Our traffic has increased ten times since October 7, and we need your help to cover our increased expenses. Support our journalists with a donation today. https://mondoweiss.net/2024/03/operation-al-aqsa-flood-day-175-icj-orders-israel-to-stop-famine-in-gaza-as-israel-continues-to-raid-hospitals/
    MONDOWEISS.NET
    ‘Operation Al-Aqsa Flood’ Day 175: ICJ orders Israel to stop famine in Gaza as Israel continues to raid hospitals
    The International Court of Justice imposed new provisional measures in South Africa’s case against Israel for its genocide in Gaza, ordering Israel to ensure the entry of food and other supplies in order to stop the spreading famine.
    0 Comments 0 Shares 16582 Views
  • ‘Operation Al-Aqsa Flood’ Day 175: ICJ orders Israel to stop famine in Gaza as Israel continues to raid hospitals
    The International Court of Justice imposed new provisional measures in South Africa’s case against Israel for its genocide in Gaza, ordering Israel to ensure the entry of food and other supplies in order to stop the spreading famine.

    Qassam MuaddiMarch 29, 2024
    Two injured Palestinian children are being treated by doctors on the floor of a hospital in southern Gaza, following Israeli airstrikes.
    Injured Palestinian children are brought to Abu Youssef Al-Najjar Hospital in Rafah for treatment following Israeli attacks on the southern Gaza Strip,on March 29, 2024. (Ahmed Ibrahim/APA Images)
    Casualties

    32,623 + killed* and at least 75,092 wounded in the Gaza Strip.
    450+ Palestinians killed in the occupied West Bank and East Jerusalem.**
    Israel revises its estimated October 7 death toll down from 1,400 to 1,139.
    597 Israeli soldiers have been killed since October 7, and at least 3,221 injured.***
    *Gaza’s Ministry of Health confirmed this figure on its Telegram channel. Some rights groups estimate the death toll to be much higher when accounting for those presumed dead.

    ** The death toll in the West Bank and Jerusalem is not updated regularly. According to the PA’s Ministry of Health on March 17, this is the latest figure.

    *** This figure is released by the Israeli military, showing the soldiers whose names “were allowed to be published.”

    Key Developments

    Israeli forces killed 71 Palestinians and wounded 112 in air and artillery strikes across the Gaza Strip.
    Israel’s raid into al-Shifa hospital enters its 12th day, destroying more buildings in the vicinity of the hospital.
    Israel releases 102 Palestinians detained from Gaza in recent weeks.
    Israel admits eight soldiers wounded in 24 hour period as fighting between Israeli army and Palestinian resistance intensifies in Gaza City and in Khan Younis.
    ICJ orders new provisional measures in South Africa’s genocide case against Srael, including provisions to prevent famine.
    North Gaza-based journalist Bayan Abu Sultan, who was feared missing since March 19 after reporting that Israeli forces killed her brother in front of her, reappears on Twitter and confirms that she is alive.
    At least 40 Syrian soldiers and Hezbollah fighters killed in Israeli strikes on Aleppo, Syria.
    UN special rapporteur for Palestine says, “there is enough grounds to believe that Israel is committing genocide.”
    West Bank: One Palestinian teenager was wounded in al-Fawwar refugee camp south of Hebron, in an Israeli raid.
    West Bank: Israel raids Nablus and the refugee camps of Shu’fat and Qalandia north of Jerusalem.
    71 Palestinians killed, death toll rises to 32,623

    The Palestinian health ministry announced in a statement on Thursday that 71 Palestinians were killed in Israeli strikes across the Gaza Strip, while 112 others were wounded in the past day.

    In Gaza City, the Israeli army continued its raid on al-Shifa Hospital for the 12th day. Local sources reported that Israeli forces burned and demolished several buildings in the surroundings of al-Shifa.

    Medical sources said that Israeli forces continue to hold 160 Palestinians, including medical staff, in the Human Development building in the al-Shifa complex.

    In Deir al-Balah, in the center Gaza Strip, Israeli warships opened fire at Palestinian homes on the beachfront. In Al-Maghazi refugee camp, east of Deir al-Balah, an Israeli strike on the Mousa family home killed six people, including both parents and four children, wounding several of their neighbors.

    In Khan Younis, Israeli strikes killed 12 Palestinians, while a nurse was reported killed by Israeli troops at the Nasser hospital.

    In Rafah, in southern Gaza, Israeli strikes on the east and center of the city killed at least 12 Palestinians, including children.

    Viral journalist reported missing reappears, Israel releases 102 Gaza detainees

    The Israeli army released 102 Palestinians who were detained from the Gaza Strip and held in Israeli custody for several days and weeks, according to local media reports.

    According to the Palestinian Red Crescent Society, nine of the released are paramedics who work for the society and who were detained for 46 days. Three of the released were taken to some of the few remaining operating hospitals in Gaza to be treated from the effects of torture, the group said.

    Meanwhile, Palestinian journalist Bayan Abu Sultan, who was reported missing in the surroundings of al-Shifa since March 19, posted on social media Thursday for the first time in 12 days.

    “I survived,” Bayan wrote on Thursday on X. Her last tweet before she disappeared read “Israeli forces killed my only brother in front of my eyes.”

    Bayan is one of the few Palestinian journalists still reporting from Gaza City and the north. She and her family were staying in the vicinity of al-Shifa Hospital, where her family returned after being displaced in the early weeks of the Israeli assault when her brother was killed.

    After activists and journalists began sounding the alarm over Bayan’s feared disappearance, Reporters Without Borders demanded in a statement that Israeli forces provide information about Bayan’s whereabouts, assuming that she was detained.

    Palestinians remaining in Gaza City continue to face severe shortages of supplies, especially of food. “Hunger, the shortage of goods and skyrocketing prices have made people [in Gaza City] lose taste for life,” Huda Amer, another Gaza-city-based journalist, told Mondoweiss. “We hear bombings and shootings in the street”, she added.

    UN rapporteur says ‘enough grounds’ for genocide in Gaza

    The United Nations Special Rapporteur on the Occupied Palestinian Territories, Francesca Albanese, said that there are “enough grounds” to believe that Israel is committing genocide against the Palestinian people in the Gaza Strip.

    Albanese made her remarks on Thursday during the presentation of her report entitled “Anatomy of a Genocide” to the UN Human Rights Council in Geneva.

    The report, which was released earlier this week, indicated that Israel was violating three of the five acts described in the Genocide Convention.

    Albanese said that she has received threats because of her report, and that she has been pressured and “attacked” since the beginning of her mandate.

    Commenting on Albanese’s report, the White House’s spokesperson Mathew Miller accused Albanese of “making antisemitic comments,” and that the entire post of human rights rapporteur for the occupied Palestinian Territories was “unproductive.” In February, Israel denied Albanese entry to the country.

    On Thursday, the International Court of Justice ordered a new set of provisional measures to prevent genocide, including provisions to prevent famine.

    The measures were requested by South Africa as part of its ongoing case against Israel at the international court.

    The ICJ judges noted that “Palestinians are no longer facing the risk of famine … but famine is setting in”. The court ordered Israel to ensure the “unhindered provision at scale by all concerned of urgently needed basic services and humanitarian assistance,” including food, water, fuel, and medical supplies. The order is legally binding, though, like the initial provisional measures granted by the court back in January, and since ignored by Israel, the court does not have an enforcement mechanism.

    Already, 31 Palestinians, mostly children, have died of food shortage in the Gaza Strip since Israel imposed a total blockade of food, water, electricity, and fuel on the 2 million people living there in the immediate aftermath of October 7.

    Israeli army wounds on Palestinian, raids West Bank towns

    A Palestinian man was wounded in the stomach by Israeli forces on Thursday night during an Israeli military raid on the al-Fawwar refugee camp, south of Hebron in the occupied West Bank.

    Local media sources reported that Israeli forces fired light flares before entering the camp, and that they were confronted by local youth throwing stones. Israeli troops responded with live fire, wounding one man.

    Israeli forces also raided Shu’fat and Qalandia, north of Jerusalem, and Nablus in the northern West Bank.

    Meanwhile, Israeli forces continue to impose tight control on checkpoints in the Jordan Valley as they continue to search for the gunman behind yesterday’s shooting at an Israeli settlers’ bus north of Jericho, which wounded three Israelis.

    Israel has arrested more than 7,800 Palestinians since October 7. Currently, at least 9,100 Palestinians are held in Israeli prisons, including 50 women, 200 children, and more than 3500 detainees without charges.

    https://mondoweiss.net/2024/03/operation-al-aqsa-flood-day-175-icj-orders-israel-to-stop-famine-in-gaza-as-israel-continues-to-raid-hospitals/
    ‘Operation Al-Aqsa Flood’ Day 175: ICJ orders Israel to stop famine in Gaza as Israel continues to raid hospitals The International Court of Justice imposed new provisional measures in South Africa’s case against Israel for its genocide in Gaza, ordering Israel to ensure the entry of food and other supplies in order to stop the spreading famine. Qassam MuaddiMarch 29, 2024 Two injured Palestinian children are being treated by doctors on the floor of a hospital in southern Gaza, following Israeli airstrikes. Injured Palestinian children are brought to Abu Youssef Al-Najjar Hospital in Rafah for treatment following Israeli attacks on the southern Gaza Strip,on March 29, 2024. (Ahmed Ibrahim/APA Images) Casualties 32,623 + killed* and at least 75,092 wounded in the Gaza Strip. 450+ Palestinians killed in the occupied West Bank and East Jerusalem.** Israel revises its estimated October 7 death toll down from 1,400 to 1,139. 597 Israeli soldiers have been killed since October 7, and at least 3,221 injured.*** *Gaza’s Ministry of Health confirmed this figure on its Telegram channel. Some rights groups estimate the death toll to be much higher when accounting for those presumed dead. ** The death toll in the West Bank and Jerusalem is not updated regularly. According to the PA’s Ministry of Health on March 17, this is the latest figure. *** This figure is released by the Israeli military, showing the soldiers whose names “were allowed to be published.” Key Developments Israeli forces killed 71 Palestinians and wounded 112 in air and artillery strikes across the Gaza Strip. Israel’s raid into al-Shifa hospital enters its 12th day, destroying more buildings in the vicinity of the hospital. Israel releases 102 Palestinians detained from Gaza in recent weeks. Israel admits eight soldiers wounded in 24 hour period as fighting between Israeli army and Palestinian resistance intensifies in Gaza City and in Khan Younis. ICJ orders new provisional measures in South Africa’s genocide case against Srael, including provisions to prevent famine. North Gaza-based journalist Bayan Abu Sultan, who was feared missing since March 19 after reporting that Israeli forces killed her brother in front of her, reappears on Twitter and confirms that she is alive. At least 40 Syrian soldiers and Hezbollah fighters killed in Israeli strikes on Aleppo, Syria. UN special rapporteur for Palestine says, “there is enough grounds to believe that Israel is committing genocide.” West Bank: One Palestinian teenager was wounded in al-Fawwar refugee camp south of Hebron, in an Israeli raid. West Bank: Israel raids Nablus and the refugee camps of Shu’fat and Qalandia north of Jerusalem. 71 Palestinians killed, death toll rises to 32,623 The Palestinian health ministry announced in a statement on Thursday that 71 Palestinians were killed in Israeli strikes across the Gaza Strip, while 112 others were wounded in the past day. In Gaza City, the Israeli army continued its raid on al-Shifa Hospital for the 12th day. Local sources reported that Israeli forces burned and demolished several buildings in the surroundings of al-Shifa. Medical sources said that Israeli forces continue to hold 160 Palestinians, including medical staff, in the Human Development building in the al-Shifa complex. In Deir al-Balah, in the center Gaza Strip, Israeli warships opened fire at Palestinian homes on the beachfront. In Al-Maghazi refugee camp, east of Deir al-Balah, an Israeli strike on the Mousa family home killed six people, including both parents and four children, wounding several of their neighbors. In Khan Younis, Israeli strikes killed 12 Palestinians, while a nurse was reported killed by Israeli troops at the Nasser hospital. In Rafah, in southern Gaza, Israeli strikes on the east and center of the city killed at least 12 Palestinians, including children. Viral journalist reported missing reappears, Israel releases 102 Gaza detainees The Israeli army released 102 Palestinians who were detained from the Gaza Strip and held in Israeli custody for several days and weeks, according to local media reports. According to the Palestinian Red Crescent Society, nine of the released are paramedics who work for the society and who were detained for 46 days. Three of the released were taken to some of the few remaining operating hospitals in Gaza to be treated from the effects of torture, the group said. Meanwhile, Palestinian journalist Bayan Abu Sultan, who was reported missing in the surroundings of al-Shifa since March 19, posted on social media Thursday for the first time in 12 days. “I survived,” Bayan wrote on Thursday on X. Her last tweet before she disappeared read “Israeli forces killed my only brother in front of my eyes.” Bayan is one of the few Palestinian journalists still reporting from Gaza City and the north. She and her family were staying in the vicinity of al-Shifa Hospital, where her family returned after being displaced in the early weeks of the Israeli assault when her brother was killed. After activists and journalists began sounding the alarm over Bayan’s feared disappearance, Reporters Without Borders demanded in a statement that Israeli forces provide information about Bayan’s whereabouts, assuming that she was detained. Palestinians remaining in Gaza City continue to face severe shortages of supplies, especially of food. “Hunger, the shortage of goods and skyrocketing prices have made people [in Gaza City] lose taste for life,” Huda Amer, another Gaza-city-based journalist, told Mondoweiss. “We hear bombings and shootings in the street”, she added. UN rapporteur says ‘enough grounds’ for genocide in Gaza The United Nations Special Rapporteur on the Occupied Palestinian Territories, Francesca Albanese, said that there are “enough grounds” to believe that Israel is committing genocide against the Palestinian people in the Gaza Strip. Albanese made her remarks on Thursday during the presentation of her report entitled “Anatomy of a Genocide” to the UN Human Rights Council in Geneva. The report, which was released earlier this week, indicated that Israel was violating three of the five acts described in the Genocide Convention. Albanese said that she has received threats because of her report, and that she has been pressured and “attacked” since the beginning of her mandate. Commenting on Albanese’s report, the White House’s spokesperson Mathew Miller accused Albanese of “making antisemitic comments,” and that the entire post of human rights rapporteur for the occupied Palestinian Territories was “unproductive.” In February, Israel denied Albanese entry to the country. On Thursday, the International Court of Justice ordered a new set of provisional measures to prevent genocide, including provisions to prevent famine. The measures were requested by South Africa as part of its ongoing case against Israel at the international court. The ICJ judges noted that “Palestinians are no longer facing the risk of famine … but famine is setting in”. The court ordered Israel to ensure the “unhindered provision at scale by all concerned of urgently needed basic services and humanitarian assistance,” including food, water, fuel, and medical supplies. The order is legally binding, though, like the initial provisional measures granted by the court back in January, and since ignored by Israel, the court does not have an enforcement mechanism. Already, 31 Palestinians, mostly children, have died of food shortage in the Gaza Strip since Israel imposed a total blockade of food, water, electricity, and fuel on the 2 million people living there in the immediate aftermath of October 7. Israeli army wounds on Palestinian, raids West Bank towns A Palestinian man was wounded in the stomach by Israeli forces on Thursday night during an Israeli military raid on the al-Fawwar refugee camp, south of Hebron in the occupied West Bank. Local media sources reported that Israeli forces fired light flares before entering the camp, and that they were confronted by local youth throwing stones. Israeli troops responded with live fire, wounding one man. Israeli forces also raided Shu’fat and Qalandia, north of Jerusalem, and Nablus in the northern West Bank. Meanwhile, Israeli forces continue to impose tight control on checkpoints in the Jordan Valley as they continue to search for the gunman behind yesterday’s shooting at an Israeli settlers’ bus north of Jericho, which wounded three Israelis. Israel has arrested more than 7,800 Palestinians since October 7. Currently, at least 9,100 Palestinians are held in Israeli prisons, including 50 women, 200 children, and more than 3500 detainees without charges. https://mondoweiss.net/2024/03/operation-al-aqsa-flood-day-175-icj-orders-israel-to-stop-famine-in-gaza-as-israel-continues-to-raid-hospitals/
    MONDOWEISS.NET
    ‘Operation Al-Aqsa Flood’ Day 175: ICJ orders Israel to stop famine in Gaza as Israel continues to raid hospitals
    The International Court of Justice imposed new provisional measures in South Africa’s case against Israel for its genocide in Gaza, ordering Israel to ensure the entry of food and other supplies in order to stop the spreading famine.
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  • Destroying Super Immunity & Getting Rid of That Annoying Cough
    Dr. Syed Haider

    I made it through multiple upper respiratory illnesses affecting my wife and kids over the last year without getting sick myself.

    The biggest difference maker seemed to be spending a lot of time outdoors in sunny Puerto Rico.

    It’s not just about the vitamin D that you get in the afternoons, it’s also about the lack of blue light toxicity you get the rest of the day from glass filtered indoor sunlight (or artificial lights).

    Blue light in the visible spectrum needs to be balanced by the naturally present infrared and UV spectrum in natural sunlight. Unfortunately both are blocked by typical window glass.


    Anyway, my long run of seemingly bulletproof immunity came to an inglorious end when I finally succumbed to what had been plaguing my nuclear family for a couple weeks: it began with a tickle in my throat, then progressed to a mild sore throat, stuffy and runny nose, bad a cough, and fatigue. It was rough going for a day or two. Hard to sleep with all the coughing.

    My post mortem analysis of what went wrong: I visited family overseas, where they live in an apartment full of artificial light and not much direct sun. I did my best to get outside, but couldnt do it anywhere near as much as I used to at home. Then (perhaps more or less important?) I started including once a week “stress test days” (nee cheat days) on my carnivore diet. That turned into a general laxity during my regular carnivore diet days, including eating out and being exposed to ubiquitous seed oils.

    Then one day I was enjoying my meat dish at a local restaurant and decided spur of the moment (always a mistake) to try the side dish I would have normally skipped. Unfortunately it was probably the worst possible side I could have indulged in: a nightshade veggie bomb comprising tomatoes, potatoes, eggplant and various kinds of peppers.

    Nightshade vegetables are notoriously toxic (despite mainstream claims that the toxins are neutralized by cooking), especially for those with a history of autoimmune disease, or leaky gut. They are also problematic for anyone with a history of allergic disorders or MCAS. It doesn’t help that traditional methods of picking and preparation that minimized the toxicity for otherwise healthy people are no longer followed.

    Pin on Hold the tomato
    Almost immediately after consuming this side dish I started to feel that first tickle in my throat and it was a slow downhill roll from there. Took 2-3 days, during which I had enough of a chance to head it off with some high dose vitamin C, but I’m one of those people who usually prefers to let nature take its course (maybe don’t do this in our current environment of repeated COVID infections, with all the problems they can bring).

    Once the illness got started I began to notice very clearly that what I ate had an almost immediate impact on how I felt. I think it probably required the sensitization of having been strictly carnivore for weeks beforehand.

    Thank you for reading Dr. Syed Haider. This post is public so feel free to share it.

    Share

    I could tell when I ate high histamine fruits or vegetables that my symptoms would worsen significantly, I might get an instant headache, stuffy nose, worsening cough, fatigue, dizziness, and even occasional anger outbursts that had plagued me before the carnivore experiment.

    All these can be due to histamine intolerance. When you’re sick or already exposed to something that lowers your histamine tolerance, adding histamine-containing foods or those that tend to liberate histamine is just added fuel for the fire.

    Histamine Intolerance Doctor Gilbert AZ
    Anyway this has been going around (not surprising since it is winter). Some people get bad diarrhea, for others it’s the cough that’s the worst.

    If you treat this early in the first day or two you can usually cut it short within the first week. If not then many people end up being somewhat under the weather for a couple weeks and the unlucky ones have lingering symptoms for many weeks. It’s not necessarily anything new, it happened before COVID too. Now people are hyperaware of it, and for good reason, because the current iterations are often due to the COVID bioweapon which damages every organ system.

    Whether or not COVID was diagnosed you can usually treat a cough heavy post viral syndrome with key lifestyle changes like avoiding airway irritants (eg use an air filter) low or even no carb (but first try a good quality medicinal honey 1-3 teaspoons dissolved in warm water 1-3 times a day), avoiding trigger foods, plenty of direct sunlight, good sleep; supplements from mygotostack.com like vitamin C, D, zinc, quercetin, turmeric, nigella sativa; and prescription meds from mygotodoc.com like: ivermectin and LDN (we can’t prescribe codeine for cough online since its a controlled substance).

    Other effective treatments include IV vitamin C, IV ozone, HBOT, or what’s easier and nearly as effective: a home oxygen concentrator a couple hours a day,

    However one of the best and most underappreciated ways to get rid of a lingering non productive (dry) cough is simple breathwork.

    That’s because it’s not always just a persistent infection or inflammation that leads to a persistent cough, it may be that, but it is also often a disordered breathing pattern that can develop after just a couple days of illness. This pattern becomes imprinted on the nervous system and can be hard to shake. The longer you leave it unaddressed the longer it may continue. The more you cough the more likely you are to keep coughing, and the less you cough the more likely you are to stop coughing.

    Now, when most people think of breathwork they think of deep breathing exercises. But deep breathing is usually a trigger for a coughing fit rather than any kind of solution (during my long COVID illness I also found it can also worsen anxiety).

    The real fix for a persistent cough (and anxiety) due to a disordered nervous system is often in breathing less, while becoming aware of the impending urge to cough and trying to head it off and suppress it.

    Practitioners of the Buteyko breathing method have a great exercise for stopping a persistent dry cough.

    Share

    When you feel the urge to cough you press your hand over your mouth, swallow and hold your breath for 5 seconds while telling yourself you don’t need to cough. Then start breathing slow and shallow through the nose, keeping your hand over your mouth. Imagine the air going in one nostril and out the other in a circle (obviously this is not actually happening it just helps keep the breathing light and not irritating to the throat, partly a psychological phenomenon).

    Do this whenever you feel the urge to cough during the day, and you’ll see that it often works rather well and makes you more aware of what triggers the coughing. Unless there is something more serious going on (don’t nocebo yourself, just assume there is not) it usually only takes 1-3 days of this to retrain your nervous system and end the cough for good.

    You can also check out other Buteyko and pranayama yoga breathing methods (like alternate nostril breathing) for stopping a cough on YouTube:


    If there is residual inflammation, often manifested by a post nasal drip irritating the throat leading to coughing fits (easy to test if you have this, just lie down flat and see if you start coughing, or get worse, within a minute or so), it’s also important to avoid trigger foods that raise histamine or lead your own body to release histamine.

    Some common ones include: the nightshades I mentioned (tomatoes, potatoes, eggplant, all peppers), bananas, strawberries, mangoes, citrus fruits, avocado, chocolate, dairy, preserved or canned meats and fish, leftover meat and fish, lentils, beans, alcohol, tea, coffee and there may be some that are individual specific (think of any foods that in small or large quantities have caused you problems in the past).

    If you don’t go low or no carb, then also avoid grains until better as they tend to be pro inflammatory.

    Fish oil supplements have a short term anti-inflammatory effect that may lead to a longer term proinflammatory outcome. I’m not clear on all the science and implications here, but you can check out Chris Masterjohn’s work on the topic. Generally speaking it seems to be fine to eat fatty fish for the Omega 3s, but most people should probably avoid the high dose supplementation currently recommended by some groups.

    Another key lifestyle measure that works great for the post nasal drip is lifting your head at night using 2-3 pillows (or a wedge pillow - also helps with chronic reflux), and even propping yourself up against the headboard or wall behind your bed. Might be uncomfortable at first, but it’s better than a night of hacking up your lungs.

    Manage Acid Reflux & more: EZsleep Wedge| EQUANIMO
    I’ve also used pieces of chewed and softened licorice root to help cover up the irritating sensation of a post nasal drip while sleeping.

    Using a neti pot a few times a day may also help with this, and you can add things like turmeric, hydrogen peroxide, iodine, or just go with the usual salt water flush.

    If there is a persistent infection then more drastic measures will be needed including the IV methods mentioned above, and you can consider nebulization of peroxide.

    Promising studies have been done on more exotic methods of relieving a cough such as nebulizing honey, drinking a mixture of honey and coffee syrup dissolved in water, and inhaling a very dilute mixture of capsaicin (from cayenne peppers - which can help with both cough and post nasal drop, and other than snorting or otherwise breathing it in, you can also mix it with honey or water and take it orally as an antihistamine).

    Finally, the most powerful herb I know of for insomnia and anxiety is the sedative-hypnotic mulungu bark, and it is also effective in treating various kinds of coughs.

    Let me know below if you’ve gotten sick this winter, and what you swear by to get better, especially what works for a prolonged dry nagging cough.

    https://blog.mygotodoc.com/p/destroying-super-immunity-and-getting

    https://telegra.ph/Destroying-Super-Immunity--Getting-Rid-of-That-Annoying-Cough-03-20
    Destroying Super Immunity & Getting Rid of That Annoying Cough Dr. Syed Haider I made it through multiple upper respiratory illnesses affecting my wife and kids over the last year without getting sick myself. The biggest difference maker seemed to be spending a lot of time outdoors in sunny Puerto Rico. It’s not just about the vitamin D that you get in the afternoons, it’s also about the lack of blue light toxicity you get the rest of the day from glass filtered indoor sunlight (or artificial lights). Blue light in the visible spectrum needs to be balanced by the naturally present infrared and UV spectrum in natural sunlight. Unfortunately both are blocked by typical window glass. Anyway, my long run of seemingly bulletproof immunity came to an inglorious end when I finally succumbed to what had been plaguing my nuclear family for a couple weeks: it began with a tickle in my throat, then progressed to a mild sore throat, stuffy and runny nose, bad a cough, and fatigue. It was rough going for a day or two. Hard to sleep with all the coughing. My post mortem analysis of what went wrong: I visited family overseas, where they live in an apartment full of artificial light and not much direct sun. I did my best to get outside, but couldnt do it anywhere near as much as I used to at home. Then (perhaps more or less important?) I started including once a week “stress test days” (nee cheat days) on my carnivore diet. That turned into a general laxity during my regular carnivore diet days, including eating out and being exposed to ubiquitous seed oils. Then one day I was enjoying my meat dish at a local restaurant and decided spur of the moment (always a mistake) to try the side dish I would have normally skipped. Unfortunately it was probably the worst possible side I could have indulged in: a nightshade veggie bomb comprising tomatoes, potatoes, eggplant and various kinds of peppers. Nightshade vegetables are notoriously toxic (despite mainstream claims that the toxins are neutralized by cooking), especially for those with a history of autoimmune disease, or leaky gut. They are also problematic for anyone with a history of allergic disorders or MCAS. It doesn’t help that traditional methods of picking and preparation that minimized the toxicity for otherwise healthy people are no longer followed. Pin on Hold the tomato Almost immediately after consuming this side dish I started to feel that first tickle in my throat and it was a slow downhill roll from there. Took 2-3 days, during which I had enough of a chance to head it off with some high dose vitamin C, but I’m one of those people who usually prefers to let nature take its course (maybe don’t do this in our current environment of repeated COVID infections, with all the problems they can bring). Once the illness got started I began to notice very clearly that what I ate had an almost immediate impact on how I felt. I think it probably required the sensitization of having been strictly carnivore for weeks beforehand. Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share I could tell when I ate high histamine fruits or vegetables that my symptoms would worsen significantly, I might get an instant headache, stuffy nose, worsening cough, fatigue, dizziness, and even occasional anger outbursts that had plagued me before the carnivore experiment. All these can be due to histamine intolerance. When you’re sick or already exposed to something that lowers your histamine tolerance, adding histamine-containing foods or those that tend to liberate histamine is just added fuel for the fire. Histamine Intolerance Doctor Gilbert AZ Anyway this has been going around (not surprising since it is winter). Some people get bad diarrhea, for others it’s the cough that’s the worst. If you treat this early in the first day or two you can usually cut it short within the first week. If not then many people end up being somewhat under the weather for a couple weeks and the unlucky ones have lingering symptoms for many weeks. It’s not necessarily anything new, it happened before COVID too. Now people are hyperaware of it, and for good reason, because the current iterations are often due to the COVID bioweapon which damages every organ system. Whether or not COVID was diagnosed you can usually treat a cough heavy post viral syndrome with key lifestyle changes like avoiding airway irritants (eg use an air filter) low or even no carb (but first try a good quality medicinal honey 1-3 teaspoons dissolved in warm water 1-3 times a day), avoiding trigger foods, plenty of direct sunlight, good sleep; supplements from mygotostack.com like vitamin C, D, zinc, quercetin, turmeric, nigella sativa; and prescription meds from mygotodoc.com like: ivermectin and LDN (we can’t prescribe codeine for cough online since its a controlled substance). Other effective treatments include IV vitamin C, IV ozone, HBOT, or what’s easier and nearly as effective: a home oxygen concentrator a couple hours a day, However one of the best and most underappreciated ways to get rid of a lingering non productive (dry) cough is simple breathwork. That’s because it’s not always just a persistent infection or inflammation that leads to a persistent cough, it may be that, but it is also often a disordered breathing pattern that can develop after just a couple days of illness. This pattern becomes imprinted on the nervous system and can be hard to shake. The longer you leave it unaddressed the longer it may continue. The more you cough the more likely you are to keep coughing, and the less you cough the more likely you are to stop coughing. Now, when most people think of breathwork they think of deep breathing exercises. But deep breathing is usually a trigger for a coughing fit rather than any kind of solution (during my long COVID illness I also found it can also worsen anxiety). The real fix for a persistent cough (and anxiety) due to a disordered nervous system is often in breathing less, while becoming aware of the impending urge to cough and trying to head it off and suppress it. Practitioners of the Buteyko breathing method have a great exercise for stopping a persistent dry cough. Share When you feel the urge to cough you press your hand over your mouth, swallow and hold your breath for 5 seconds while telling yourself you don’t need to cough. Then start breathing slow and shallow through the nose, keeping your hand over your mouth. Imagine the air going in one nostril and out the other in a circle (obviously this is not actually happening it just helps keep the breathing light and not irritating to the throat, partly a psychological phenomenon). Do this whenever you feel the urge to cough during the day, and you’ll see that it often works rather well and makes you more aware of what triggers the coughing. Unless there is something more serious going on (don’t nocebo yourself, just assume there is not) it usually only takes 1-3 days of this to retrain your nervous system and end the cough for good. You can also check out other Buteyko and pranayama yoga breathing methods (like alternate nostril breathing) for stopping a cough on YouTube: If there is residual inflammation, often manifested by a post nasal drip irritating the throat leading to coughing fits (easy to test if you have this, just lie down flat and see if you start coughing, or get worse, within a minute or so), it’s also important to avoid trigger foods that raise histamine or lead your own body to release histamine. Some common ones include: the nightshades I mentioned (tomatoes, potatoes, eggplant, all peppers), bananas, strawberries, mangoes, citrus fruits, avocado, chocolate, dairy, preserved or canned meats and fish, leftover meat and fish, lentils, beans, alcohol, tea, coffee and there may be some that are individual specific (think of any foods that in small or large quantities have caused you problems in the past). If you don’t go low or no carb, then also avoid grains until better as they tend to be pro inflammatory. Fish oil supplements have a short term anti-inflammatory effect that may lead to a longer term proinflammatory outcome. I’m not clear on all the science and implications here, but you can check out Chris Masterjohn’s work on the topic. Generally speaking it seems to be fine to eat fatty fish for the Omega 3s, but most people should probably avoid the high dose supplementation currently recommended by some groups. Another key lifestyle measure that works great for the post nasal drip is lifting your head at night using 2-3 pillows (or a wedge pillow - also helps with chronic reflux), and even propping yourself up against the headboard or wall behind your bed. Might be uncomfortable at first, but it’s better than a night of hacking up your lungs. Manage Acid Reflux & more: EZsleep Wedge| EQUANIMO I’ve also used pieces of chewed and softened licorice root to help cover up the irritating sensation of a post nasal drip while sleeping. Using a neti pot a few times a day may also help with this, and you can add things like turmeric, hydrogen peroxide, iodine, or just go with the usual salt water flush. If there is a persistent infection then more drastic measures will be needed including the IV methods mentioned above, and you can consider nebulization of peroxide. Promising studies have been done on more exotic methods of relieving a cough such as nebulizing honey, drinking a mixture of honey and coffee syrup dissolved in water, and inhaling a very dilute mixture of capsaicin (from cayenne peppers - which can help with both cough and post nasal drop, and other than snorting or otherwise breathing it in, you can also mix it with honey or water and take it orally as an antihistamine). Finally, the most powerful herb I know of for insomnia and anxiety is the sedative-hypnotic mulungu bark, and it is also effective in treating various kinds of coughs. Let me know below if you’ve gotten sick this winter, and what you swear by to get better, especially what works for a prolonged dry nagging cough. https://blog.mygotodoc.com/p/destroying-super-immunity-and-getting 👉https://telegra.ph/Destroying-Super-Immunity--Getting-Rid-of-That-Annoying-Cough-03-20
    BLOG.MYGOTODOC.COM
    Destroying Super Immunity & Getting Rid of That Annoying Cough
    I made it through multiple upper respiratory illnesses affecting my wife and kids over the last year without getting sick myself. The biggest difference maker seemed to be spending a lot of time outdoors in sunny Puerto Rico. It’s not just about the vitamin D that you get in the afternoons, it’s also about the lack of blue light toxicity you get the rest of the day from glass filtered indoor sunlight (or artificial lights).
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  • My training in mechanistic toxicology was repeatedly useful in helping teams foresee, avoid or understand such problems.

    So I understand deeply how to design molecules and also how to interrogate them for their prospects to bring about desired effects and crucially to discern risks of harms. I don’t think it’s too great a claim to say that there isn’t anyone better qualified than I am to do this in relation to these novel treatments.

    I’m going to go directly to the charges.
    These injections have been carefully designed to intentionally cause toxicity in those injected with them.
    I can detect at least three, separate features of these injections which would be expected to injure, to kill or to reduce fertility in survivors. These are not mistakes. Each are so obviously deliberate to anyone who has a history of involvement in rational drug design for new medicines.

    At least two features are common to every injection purporting to be a “covid vaccine”. First, the mRNA nature of the major products. Second, the lipid nanoparticle nature of the formulations in which they are encapsulated.

    The mRNA is genetic code for a chosen protein. Regardless of what the protein is, once the human body is caused to express it, it will be recognized as foreign and attacked by their own immune system. Depending on details we cannot know, just by looking at the glass vials, some people will be injured as a result of this lethal autoimmune attack. Others will be killed, the time taken to die & their suffering before they die will vary. It’ll look like the normal range of illnesses. There will simply be more of them.

    Because of the lipid nano particle formulation, some of the injected materials will accumulate in the ovaries (possibly also the testicles). This homing property in reproductive tissue has been known about for more than a decade. The effect will be a lowering of fertility affecting every stage of reproduction.
    I can bring detailed rationales for each of these claims as well as several others.

    I also have an usual piece of evidence, given the crimes I claim have been committed. I had worked out part of this assault before any purported vaccine had received its fraudulent authorization.
    Having done so, with another author, I wrote an open letter to the European Medicines Authority in early December 2020, which is attached below. In it, we warn of the harms which we anticipated. It has been more than upsetting to watch them come true, the last taking a year, the adverse effects on fertility.
    All-causes mortality is elevated almost everywhere in the world that these products have been widely used and live births sharply reduced.
    https://2020news.de/wp-content/uploads/2020/12/Wodarg_Yeadon_EMA_Petition_Pfizer_Trial_FINAL_01DEC2020_EN_unsigned_with_Exhibits.pdf

    I look forward to the opportunity to speak with you in considerable detail about these and other charges.

    I will publish this letter on my Telegram site, where followers will no doubt be interested to learn what the Met Police does with this information. If I may be so bold, I would invite you to think about how you plan to describe your next actions to your family and, if you have them, your children and grandchildren.

    With best wishes and thank you for your attention.

    Dr Mike Yeadon

    https://t.me/DrMikeYeadon
    My training in mechanistic toxicology was repeatedly useful in helping teams foresee, avoid or understand such problems. So I understand deeply how to design molecules and also how to interrogate them for their prospects to bring about desired effects and crucially to discern risks of harms. I don’t think it’s too great a claim to say that there isn’t anyone better qualified than I am to do this in relation to these novel treatments. I’m going to go directly to the charges. These injections have been carefully designed to intentionally cause toxicity in those injected with them. I can detect at least three, separate features of these injections which would be expected to injure, to kill or to reduce fertility in survivors. These are not mistakes. Each are so obviously deliberate to anyone who has a history of involvement in rational drug design for new medicines. At least two features are common to every injection purporting to be a “covid vaccine”. First, the mRNA nature of the major products. Second, the lipid nanoparticle nature of the formulations in which they are encapsulated. The mRNA is genetic code for a chosen protein. Regardless of what the protein is, once the human body is caused to express it, it will be recognized as foreign and attacked by their own immune system. Depending on details we cannot know, just by looking at the glass vials, some people will be injured as a result of this lethal autoimmune attack. Others will be killed, the time taken to die & their suffering before they die will vary. It’ll look like the normal range of illnesses. There will simply be more of them. Because of the lipid nano particle formulation, some of the injected materials will accumulate in the ovaries (possibly also the testicles). This homing property in reproductive tissue has been known about for more than a decade. The effect will be a lowering of fertility affecting every stage of reproduction. I can bring detailed rationales for each of these claims as well as several others. I also have an usual piece of evidence, given the crimes I claim have been committed. I had worked out part of this assault before any purported vaccine had received its fraudulent authorization. Having done so, with another author, I wrote an open letter to the European Medicines Authority in early December 2020, which is attached below. In it, we warn of the harms which we anticipated. It has been more than upsetting to watch them come true, the last taking a year, the adverse effects on fertility. All-causes mortality is elevated almost everywhere in the world that these products have been widely used and live births sharply reduced. https://2020news.de/wp-content/uploads/2020/12/Wodarg_Yeadon_EMA_Petition_Pfizer_Trial_FINAL_01DEC2020_EN_unsigned_with_Exhibits.pdf I look forward to the opportunity to speak with you in considerable detail about these and other charges. I will publish this letter on my Telegram site, where followers will no doubt be interested to learn what the Met Police does with this information. If I may be so bold, I would invite you to think about how you plan to describe your next actions to your family and, if you have them, your children and grandchildren. With best wishes and thank you for your attention. Dr Mike Yeadon 👉 https://t.me/DrMikeYeadon
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  • UN - Agenda 2030 - "Sustainable Development"

    PART 1 OF 2

    In 2015 the leaders of 193 countries signed their population up to Agenda 2030

    What is Sustainable Development (SD)?
    SD is "development that meets the needs of the present without compromising the ability of future generations to meet their own needs”

    Core Principles:

    Universality (all countries committed to whole Agenda regardless of any unique factors)

    Leaving No One Behind (all people will be included; “with unprecedented need for data to ensure this principle is met”)

    Interconnectedness and Indivisibility – no pick and mix approach to Sustainable Development Goals (SDGs) – all to be followed

    Inclusiveness – the entire population must follow

    Multi Stakeholder Partnerships – establishment seen as essential to deliver all SDG’s

    Dimensions of the Agenda (the 5Ps)
    People, Prosperity, Planet, Partnership and Peace

    Sustainable Development Goals (SDGs)
    Used to focus on areas necessary to achieve SD

    Each SDG has 8-12 targets & 1-4 indicators of progress

    SDG'S:

    Goal 1: End poverty
    Goal 2: End hunger
    Goal 3: Ensure healthy lives
    Goal 4: Quality education
    Goal 5: Gender equality
    Goal 6: Water/sanitation for all
    Goal 7: Affordable clean energy for all
    Goal 8: Economic growth/full + productive employment
    Goal 9: Resilient infrastructure, sustainable industrialization/innovation
    Goal 10: Reduce inequality within and among countries
    Goal 11: Make cities and human settlements inclusive, safe, resilient & sustainable
    Goal 12: Ensure sustainable consumption + production patterns
    Goal 13: Combat climate change
    Goal 14: Conserve/sustainably use oceans, seas & marine resources
    Goal 15: Promote sustainable use of terrestrial ecosystems, forests, deserts & land
    Goal 16: Promote inclusive societies, access to justice + accountable institutions
    Goal 17: Strengthen/revitalise the Global Partnership for SD

    Link
    UN - Agenda 2030 - "Sustainable Development" PART 1 OF 2 In 2015 the leaders of 193 countries signed their population up to Agenda 2030 What is Sustainable Development (SD)? SD is "development that meets the needs of the present without compromising the ability of future generations to meet their own needs” Core Principles: Universality (all countries committed to whole Agenda regardless of any unique factors) Leaving No One Behind (all people will be included; “with unprecedented need for data to ensure this principle is met”) Interconnectedness and Indivisibility – no pick and mix approach to Sustainable Development Goals (SDGs) – all to be followed Inclusiveness – the entire population must follow Multi Stakeholder Partnerships – establishment seen as essential to deliver all SDG’s Dimensions of the Agenda (the 5Ps) People, Prosperity, Planet, Partnership and Peace Sustainable Development Goals (SDGs) Used to focus on areas necessary to achieve SD Each SDG has 8-12 targets & 1-4 indicators of progress SDG'S: Goal 1: End poverty Goal 2: End hunger Goal 3: Ensure healthy lives Goal 4: Quality education Goal 5: Gender equality Goal 6: Water/sanitation for all Goal 7: Affordable clean energy for all Goal 8: Economic growth/full + productive employment Goal 9: Resilient infrastructure, sustainable industrialization/innovation Goal 10: Reduce inequality within and among countries Goal 11: Make cities and human settlements inclusive, safe, resilient & sustainable Goal 12: Ensure sustainable consumption + production patterns Goal 13: Combat climate change Goal 14: Conserve/sustainably use oceans, seas & marine resources Goal 15: Promote sustainable use of terrestrial ecosystems, forests, deserts & land Goal 16: Promote inclusive societies, access to justice + accountable institutions Goal 17: Strengthen/revitalise the Global Partnership for SD Link
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  • USING YOUR MENTAL ENERGY
    PART 120

    None can know the father, but the son; & no one can know the son, but the father.

    Only the reproductive creative #SpiritOfLife knows what you think until your thoughts become #physical facts & manifest themselves in your #body, #brain or #affairs.

    Then everyone who you come in contact with may know.

    Because the father, the intelligent creative #energy, which watches in #secret, hears your deepest #thoughts, rewards you openly & reproduces your thoughts in #PhysicalForm.
    🧠USING YOUR MENTAL ENERGY ✅PART 120 None can know the father, but the son; & no one can know the son, but the father. Only the reproductive creative #SpiritOfLife knows what you think until your thoughts become #physical facts & manifest themselves in your #body, #brain or #affairs. Then everyone who you come in contact with may know. Because the father, the intelligent creative #energy, which watches in #secret, hears your deepest #thoughts, rewards you openly & reproduces your thoughts in #PhysicalForm.
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  • 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
    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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    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.
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  • Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule
    A review paper published last week in the journal Cureus is the first peer-reviewed paper to call for a global moratorium on the COVID-19 mRNA vaccines. The authors say that reanalyzed data from the vaccine makers’ trials and high rates of serious post-injection injuries indicate the mRNA gene therapy vaccines should not have been authorized for use.

    Brenda Baletti, Ph.D.
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    Governments should endorse a global moratorium on mRNA vaccines until all questions about their safety have been thoroughly investigated, according to the authors of a new, peer-reviewed article on the COVID-19 vaccine trials and the global vaccination campaign published last week in Cureus, Journal of Medical Science.

    Cureus is a web-based peer-reviewed open-access general medical journal using prepublication peer review.

    The authors surveyed published research on the pharmaceutical companies’ vaccine trials and related adverse events. They also called for the COVID-19 vaccines to be removed immediately from the childhood immunization schedule.

    After the first reports from vaccine trials claimed they were 95% effective in preventing COVID-19, serious problems with method, execution and reporting in the trials became public, which the paper reviewed in detail.

    Evidence also shows the products never underwent adequate safety and toxicological testing, and since the vaccine rollout, researchers have identified a significant number of adverse events (AEs) and serious adverse events (SAEs).

    Authors M. Nathaniel Mead, Stephanie Seneff, Ph.D., Russ Wolfinger, Ph.D., Jessica Rose, Ph.D., Kris Denhaerynck, Ph.D., Steve Kirsch and Dr. Peter McCullough detailed the vaccines’ potential serious harms to humans, vaccine control and processing issues, the mechanisms behind AEs, the immunological reasons for vaccine inefficacy and the mortality data from the registrational trials.

    They concluded, “Federal agency approval of the COVID-19 mRNA injectable products on a blanket-coverage population-wide basis had no support from an honest assessment of all relevant registrational data and commensurate consideration of risks versus benefits.”

    They also called for the vaccines to be immediately removed from the childhood immunization schedule and for the suspension of the boosters.

    “It is unethical and unconscionable to administer an experimental vaccine to a child who has a near-zero risk of dying from COVID-19 (IFR, 0.0003%) but a well-established 2.2% risk of permanent heart damage based on the best prospective data available,” they wrote.

    Finally, the authors called for a full investigation into misconduct by the pharmaceutical companies and the regulatory agencies.

    It is the first peer-reviewed study to call for a moratorium on the COVID-19 mRNA products, Rose told The Defender.

    “Once a proper assessment of the safety and efficacy claims was made herein — upon which the emergency use authorization (EUA)’s and ultimate final authorizations were granted — it was found that the COVID-19 injectable products were neither safe nor effective,” she added.

    According to McCollough, “mRNA should never have been authorized for human use.”

    Lead author Mead told The Defender, “Our view is that any risk-benefit analysis must consider how much the presumed benefit in terms of reduced COVID-19 related mortality is offset by the potential increase in vaccine-induced mortality.”

    Here are six takeaways from the review:

    1. The COVID-19 ‘vaccines’ are reclassified gene therapies that were rushed through the regulatory process in a historically unprecedented manner

    Before the seven-month authorization process for the mRNA vaccines, no vaccine had ever gone to market without undergoing testing of at least four years, with typical timelines averaging 10 years.

    To speed the process, the companies skipped preclinical studies of potential toxicity from multiple doses and cut the typical 6-12 month observation period for identifying longer-term adverse effects and the established 10-15-year period for monitoring for long-term effects such as cancer and autoimmune disorders, the authors wrote.

    The trials prioritized documenting effective symptom reduction over SAE and mortality. This was particularly concerning, the authors argued, because mRNA products are gene therapy products reclassified as vaccines and then given EUA for the first time ever for use against a viral disease.

    However, the gene therapies’ components have not been thoroughly evaluated for safety for use as vaccines.

    There is an uninvestigated and major concern that the mRNA could transform body cells into viral protein factories — with no off-switch — that produce the spike protein for a prolonged period causing chronic systemic inflammation and immune dysfunction.

    The spike protein in the vaccine, the authors said, is associated with more severe immunopathology and other AEs than the spike protein in the virus itself.

    The authors suggested that massive government investment in mRNA technology, including hundreds of millions before the pandemic and tens of billions once it began, meant, “U.S. federal agencies were strongly biased toward successful outcomes for the registrational trials.”

    The financial incentives along with political pressures to deliver a rapid solution likely influenced a series of flawed decisions that compromised the integrity of the trials and downplayed serious scientific concerns about risks with the technology, they added.

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    2. Steps were taken in trials to overestimate vaccine efficacy

    Because the trials were designed to assess whether the mRNA vaccine reduced symptoms, they did not measure whether the vaccines prevented severe disease and death. Yet the vaccine makers repeatedly claimed that they do.

    “No large randomized double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalization, or death,” the authors wrote.

    Additionally, the number of people who contracted clinical COVID-19 in both the placebo and intervention groups was “too small to draw meaningful, pragmatic, or broad-sweeping conclusions with regard to COVID-19 morbidity and mortality.”

    Pfizer’s 95 % efficacy claims were based on 162 of 22,000 placebo recipients contracting PCR-confirmed COVID-19 compared to eight of 22,000 in the vaccine group. None of the placebo recipients died from COVID-19. In the Moderna trials, only one placebo death was attributed to COVID-19.

    There was also a much larger percentage of “suspected COVID-19 cases” in both groups, with participants showing COVID-19 symptoms but a negative PCR test. When factoring in those cases, measures of vaccine efficacy drop to about 19%.

    The trial subject pool was comprised of largely young and healthy individuals, excluding key groups — children, pregnant women, elderly and immunocompromised people — which can also obscure the vaccine’s actual efficacy and safety.

    Findings from reanalyses of data from the Pfizer trials can be interpreted as showing the vaccines made “no significant difference” in reducing all-cause mortality in the vaccinated versus unvaccinated groups at 20 weeks into the trial, the authors wrote.

    Even the six-month post-marketing data Pfizer presented to the U.S. Food and Drug Administration (FDA) showed no reduction in all-cause mortality from the vaccine.

    The authors reanalyzed that data, adjusting the analysis of deaths to better account for the fact that when Pfizer unblinded the study people from the placebo group took the vaccine, and found the vaccine group had a higher mortality rate (0.105%) than the unvaccinated group (0.0799%), which they said was a conservative estimate.

    One of the most glaring issues with the registrational trials, they noted, was that they exclusively focused on measuring risk reduction — the ratio of COVID-19 symptom rates in the vaccine group versus the placebo group — rather than measuring absolute risk reduction, which is the likelihood someone will show COVID-19 symptoms relative to people in the population at large.

    According to FDA guidelines, accounting for both approaches is crucial to avoid the misguided use of pharmaceutical products — but the data were omitted, leading to an overestimation of an intervention’s clinical utility.

    While both vaccines touted an approximately 95% risk reduction figure as their efficacy figure, the absolute risk reductions for Pfizer and Moderna’s vaccines were 0.7% and 1.1% respectively.

    “A substantial number of individuals would need to be injected in order to prevent a single mild-to-moderate case of COVID-19,” the authors wrote.

    As an example, using a conservative estimate that 119 people would need to be vaccinated to prevent infection, and assuming that COVID-19 had a 0.23% infection fatality rate, they wrote that approximately 52,000 vaccinations would be necessary to prevent a single COVID-19-related death.

    However, “Given trial misconduct and data integrity problems … the true benefit is likely to be much lower,” they wrote.

    And, they added, one would need to assess that benefit along with harms, which they estimate to be 27 deaths per 100,000 doses of Pfizer. That means, using the most conservative estimates, “for every life saved, there were 14 times more deaths caused by the modified mRNA injections.”

    They also noted that post-rollout evidence confirmed the efficacy claims were overstated. For example, two large cohort Cleveland clinic studies showed the vaccine could not confer protection against COVID-19 — instead, in those trials, more vaccinated people were more likely to contract COVID-19.

    One study showed the risk of “breakthrough” infection was significantly higher among people who were boosted and that more vaccinations resulted in a greater risk of COVID-19.

    A second study showed adults who were not “up-to-date” with their shots had a 23% lower incidence of COVID-19 than their “up-to-date” colleagues.

    3. The trials underestimated the adverse events, including death, despite evidence in the data.

    Harms were also underreported and underestimated for a number of reasons, according to the authors, a practice that tends to be common in randomized industry-sponsored vaccine trials in general and “exceptionally evident” here.

    First, because Pfizer unblinded the trial within just a few weeks of the emergency use authorization and allowed people in the placebo group to take the vaccine, there was not sufficient time to identify late-occurring harms because there was no longer a control group.

    “Was this necessary, given that none of the deaths in the Pfizer trial were attributed to COVID-19 as the primary cause, and given the very low IFR [infection fatality rate] for a relatively healthy population?” they asked.

    Also, trial coordinators were “haphazard” in their approach to monitoring AEs. They prioritized documenting events thought to be related to COVID-19 rather than to the vaccines for the first seven days and only recorded “unsolicited” AEs for 30-60 days. After that period, even very SAEs, like death, were not recorded. Even for the AEs recorded in the first seven days, they only solicited data from 20% of the population.

    None of the trial data was independently verified. “Such secrecy may have enabled the industry to more easily present an inflated and distorted estimate of the genetic injections’ benefits, along with a gross underestimation of potential harms,” they wrote.

    Subsequent analysis by Michels et al. revealed that deaths and other SAEs — like life-threatening conditions, inpatient hospitalization or extension of hospitalization, persistent or significant disability/incapacity, a congenital anomaly, or a medically significant event — did occur after the cutoff period and before the FDA advisory meeting where emergency authorization was recommended.

    During the first 33 weeks of the Pfizer trials, 38 subjects died, according to Pfizer’s own data, although independent research by Michels et al. estimated that that number is only approximately 17% of the actual projected number due to missing data.

    And after that, the rate of deaths continued to increase. Michaels et al. found Pfizer failed to report a substantial increase in the number of deaths due to cardiovascular events. They also found a consistent pattern of reporting delays on the date of the death on subjects’ case reports.

    Overall, the review authors reported that there were “twice as many cardiac deaths proportionately among vaccinated compared to unvaccinated subjects in the Pfizer trials.”

    In their discussion, the authors wrote “Based on the extended Pfizer trial findings, our person-years estimate yielded a 31% increase in overall mortality among vaccine recipients, a clear trend in the wrong direction.”

    This raises serious red flags about how the registrational trials were conducted, Mead said. “Assessments of the safety profile of the COVID-19 modified mRNA injections warrant an objective precautionary perspective, any substantial upward trend in all cause mortality within the intervention arm of the trial population reflects badly on the intervention.”

    4. Numbers of SAEs in the trials and post-rollout reporting are well-documented, despite claims to the contrary.

    Both Pfizer and Moderna found about 125 SAEs per 100,000 vaccine recipients, or one SAE for every 800 vaccines. However, because the trials excluded more vulnerable people, the authors note, even higher proportions of SAEs would be expected in the general population.

    The Fraiman et al. reanalysis of the Pfizer trial data found a significant 36% higher risk of SAEs, which included deaths and many life-threatening conditions in the vaccinated participants.

    Official SAEs for other vaccines average around only 1-2 per million. Fraiman et alestimated 1,250 SEAs per million vaccines, exceeding that benchmark by “at least 600-fold.”

    After the vaccine rollout, analyses of two large drug safety reporting systems in the U.S. and Europe identified signals for myocardial infarction, pulmonary embolism, cardio-respiratory arrest, cerebral infarction, and cerebral hemorrhage associated with both mRNA vaccines, along with ischemic stroke.

    And millions of AEs have been reported to those systems.

    Another study by Skidmore et al. estimated the total number of fatalities from the vaccines in 2021 alone was 289,789. Autopsy studies have also provided additional evidence of serious harms, including evidence that most COVID-19 mRNA vaccine-related deaths resulted from injury to the cardiovascular system.

    In multiple autopsy studies, German pathologist Aren Burkhardt documented the presence of vaccine-mRNA-produced spike proteins in blood vessel walls and brain tissues. This research helps to explain documented vaccine-induced toxicities affecting the nervous, immune, reproductive and other systems.

    The Pfizer data also showed an overwhelming number of adverse effects. According to a confidential document released in August 2022, Pfizer had documented approximately 1.6 million AEs affecting nearly every organ system, and one-third of them were classified as serious.

    In Pfizer’s trial, Michels and colleagues found a nearly 4-fold increase (OR 3.7, 95%CI 1.02-13.2, p = 0.03) in serious cardiac events (e.g., heart attack, acute coronary syndrome) in the vaccine group. Neither the original trial report nor Pfizer’s Summary Clinical Safety report acknowledged or commented on this safety signal.

    “The serious adverse events are all well documented,” Mead said. “Yet it’s surprising to see so many in the medical field continue to ignore or dismiss outright the latter half of the equation when considering all cause mortality trends.”

    5. The failure to appropriately test for safety and toxicity poses serious problems.

    Researchers have raised concerns that the mRNA technology is inherently unstable and difficult to store, which leads to batch variability and contamination linked to different rates of AEs.

    Recent findings by McKernan et al. that found Pfizers’ mRNA vaccines are contaminated with plasmid DNA that shouldn’t be present — and wasn’t present in the vaccines used in the trials – raising serious safety issues.

    That’s because “Process 1,” used in the trials to generate the vaccines involved in vitro transcription of synthetic DNA — essentially a “clean” process. However, that process isn’t viable for mass production, so the manufacturers used “Process 2,” which involves using E. coli bacteria to replicate the plasmids.

    Removing plasmids E coli. can result in residual plasmids in the vaccines and the effects of their presence is unknown.

    McKernan’s work also revealed the presence of DNA from simian virus 40 (SV40), an oncogenic DNA virus originally isolated in 1960 from contaminated polio vaccines, induces lymphomas, brain tumors, and other malignancies in laboratory animals, raising other safety concerns.

    Researchers from Cambridge published a paper in Nature in December 2023, where they found an inherent defect in the modified RNA instructions for the spike protein in COVID-19 immunizations that causes the machinery that translates the gene to the spike protein to “slip” about 10% of the time

    This process creates “frameshifts” that cause cells to produce “off-target” proteins in addition to the spike. These proteins, which developers either failed to look for or did not report to regulators, cause undesirable immune responses whose long-term effects are unknown.

    6. There are many different possible biological mechanisms that cause AEs and vaccine ineffectiveness.

    The review points readers to a series of papers that explain a number of different theories to explain the high number of AEs from the COVID-19 mRNA vaccines.

    “The mechanisms of molecular mimicry, antigen cross-reactivity, pathogenic priming, viral reactivation, immune exhaustion, and other factors related to immune dysfunction all reinforce the biological plausibility for vaccine-induced pathogenesis of malignant and autoimmune diseases,” they wrote. And these mechanisms of immune activation are distinct from the body’s response to a viral infection.

    They also note the toxic effects of the primary adjuvant, PEG, and of the spike protein itself.

    They close their analysis of the vaccines with a complex explanation for the different immunological basis for protection provided by the vaccines versus natural immunity through infection. They explain the mechanisms for vaccine failure and problems generated by the ability for the mRNA vaccines to perpetuate the emergence of new variants.

    https://childrenshealthdefense.org/defender/scientists-global-moratorium-mrna-vaccines-removal-childhood-schedule/


    https://donshafi911.blogspot.com/2024/01/scientists-call-for-global-moratorium.html
    Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule A review paper published last week in the journal Cureus is the first peer-reviewed paper to call for a global moratorium on the COVID-19 mRNA vaccines. The authors say that reanalyzed data from the vaccine makers’ trials and high rates of serious post-injection injuries indicate the mRNA gene therapy vaccines should not have been authorized for use. Brenda Baletti, Ph.D. global moratorium mrna covid vaccine feature Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. Governments should endorse a global moratorium on mRNA vaccines until all questions about their safety have been thoroughly investigated, according to the authors of a new, peer-reviewed article on the COVID-19 vaccine trials and the global vaccination campaign published last week in Cureus, Journal of Medical Science. Cureus is a web-based peer-reviewed open-access general medical journal using prepublication peer review. The authors surveyed published research on the pharmaceutical companies’ vaccine trials and related adverse events. They also called for the COVID-19 vaccines to be removed immediately from the childhood immunization schedule. After the first reports from vaccine trials claimed they were 95% effective in preventing COVID-19, serious problems with method, execution and reporting in the trials became public, which the paper reviewed in detail. Evidence also shows the products never underwent adequate safety and toxicological testing, and since the vaccine rollout, researchers have identified a significant number of adverse events (AEs) and serious adverse events (SAEs). Authors M. Nathaniel Mead, Stephanie Seneff, Ph.D., Russ Wolfinger, Ph.D., Jessica Rose, Ph.D., Kris Denhaerynck, Ph.D., Steve Kirsch and Dr. Peter McCullough detailed the vaccines’ potential serious harms to humans, vaccine control and processing issues, the mechanisms behind AEs, the immunological reasons for vaccine inefficacy and the mortality data from the registrational trials. They concluded, “Federal agency approval of the COVID-19 mRNA injectable products on a blanket-coverage population-wide basis had no support from an honest assessment of all relevant registrational data and commensurate consideration of risks versus benefits.” They also called for the vaccines to be immediately removed from the childhood immunization schedule and for the suspension of the boosters. “It is unethical and unconscionable to administer an experimental vaccine to a child who has a near-zero risk of dying from COVID-19 (IFR, 0.0003%) but a well-established 2.2% risk of permanent heart damage based on the best prospective data available,” they wrote. Finally, the authors called for a full investigation into misconduct by the pharmaceutical companies and the regulatory agencies. It is the first peer-reviewed study to call for a moratorium on the COVID-19 mRNA products, Rose told The Defender. “Once a proper assessment of the safety and efficacy claims was made herein — upon which the emergency use authorization (EUA)’s and ultimate final authorizations were granted — it was found that the COVID-19 injectable products were neither safe nor effective,” she added. According to McCollough, “mRNA should never have been authorized for human use.” Lead author Mead told The Defender, “Our view is that any risk-benefit analysis must consider how much the presumed benefit in terms of reduced COVID-19 related mortality is offset by the potential increase in vaccine-induced mortality.” Here are six takeaways from the review: 1. The COVID-19 ‘vaccines’ are reclassified gene therapies that were rushed through the regulatory process in a historically unprecedented manner Before the seven-month authorization process for the mRNA vaccines, no vaccine had ever gone to market without undergoing testing of at least four years, with typical timelines averaging 10 years. To speed the process, the companies skipped preclinical studies of potential toxicity from multiple doses and cut the typical 6-12 month observation period for identifying longer-term adverse effects and the established 10-15-year period for monitoring for long-term effects such as cancer and autoimmune disorders, the authors wrote. The trials prioritized documenting effective symptom reduction over SAE and mortality. This was particularly concerning, the authors argued, because mRNA products are gene therapy products reclassified as vaccines and then given EUA for the first time ever for use against a viral disease. However, the gene therapies’ components have not been thoroughly evaluated for safety for use as vaccines. There is an uninvestigated and major concern that the mRNA could transform body cells into viral protein factories — with no off-switch — that produce the spike protein for a prolonged period causing chronic systemic inflammation and immune dysfunction. The spike protein in the vaccine, the authors said, is associated with more severe immunopathology and other AEs than the spike protein in the virus itself. The authors suggested that massive government investment in mRNA technology, including hundreds of millions before the pandemic and tens of billions once it began, meant, “U.S. federal agencies were strongly biased toward successful outcomes for the registrational trials.” The financial incentives along with political pressures to deliver a rapid solution likely influenced a series of flawed decisions that compromised the integrity of the trials and downplayed serious scientific concerns about risks with the technology, they added. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now 2. Steps were taken in trials to overestimate vaccine efficacy Because the trials were designed to assess whether the mRNA vaccine reduced symptoms, they did not measure whether the vaccines prevented severe disease and death. Yet the vaccine makers repeatedly claimed that they do. “No large randomized double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalization, or death,” the authors wrote. Additionally, the number of people who contracted clinical COVID-19 in both the placebo and intervention groups was “too small to draw meaningful, pragmatic, or broad-sweeping conclusions with regard to COVID-19 morbidity and mortality.” Pfizer’s 95 % efficacy claims were based on 162 of 22,000 placebo recipients contracting PCR-confirmed COVID-19 compared to eight of 22,000 in the vaccine group. None of the placebo recipients died from COVID-19. In the Moderna trials, only one placebo death was attributed to COVID-19. There was also a much larger percentage of “suspected COVID-19 cases” in both groups, with participants showing COVID-19 symptoms but a negative PCR test. When factoring in those cases, measures of vaccine efficacy drop to about 19%. The trial subject pool was comprised of largely young and healthy individuals, excluding key groups — children, pregnant women, elderly and immunocompromised people — which can also obscure the vaccine’s actual efficacy and safety. Findings from reanalyses of data from the Pfizer trials can be interpreted as showing the vaccines made “no significant difference” in reducing all-cause mortality in the vaccinated versus unvaccinated groups at 20 weeks into the trial, the authors wrote. Even the six-month post-marketing data Pfizer presented to the U.S. Food and Drug Administration (FDA) showed no reduction in all-cause mortality from the vaccine. The authors reanalyzed that data, adjusting the analysis of deaths to better account for the fact that when Pfizer unblinded the study people from the placebo group took the vaccine, and found the vaccine group had a higher mortality rate (0.105%) than the unvaccinated group (0.0799%), which they said was a conservative estimate. One of the most glaring issues with the registrational trials, they noted, was that they exclusively focused on measuring risk reduction — the ratio of COVID-19 symptom rates in the vaccine group versus the placebo group — rather than measuring absolute risk reduction, which is the likelihood someone will show COVID-19 symptoms relative to people in the population at large. According to FDA guidelines, accounting for both approaches is crucial to avoid the misguided use of pharmaceutical products — but the data were omitted, leading to an overestimation of an intervention’s clinical utility. While both vaccines touted an approximately 95% risk reduction figure as their efficacy figure, the absolute risk reductions for Pfizer and Moderna’s vaccines were 0.7% and 1.1% respectively. “A substantial number of individuals would need to be injected in order to prevent a single mild-to-moderate case of COVID-19,” the authors wrote. As an example, using a conservative estimate that 119 people would need to be vaccinated to prevent infection, and assuming that COVID-19 had a 0.23% infection fatality rate, they wrote that approximately 52,000 vaccinations would be necessary to prevent a single COVID-19-related death. However, “Given trial misconduct and data integrity problems … the true benefit is likely to be much lower,” they wrote. And, they added, one would need to assess that benefit along with harms, which they estimate to be 27 deaths per 100,000 doses of Pfizer. That means, using the most conservative estimates, “for every life saved, there were 14 times more deaths caused by the modified mRNA injections.” They also noted that post-rollout evidence confirmed the efficacy claims were overstated. For example, two large cohort Cleveland clinic studies showed the vaccine could not confer protection against COVID-19 — instead, in those trials, more vaccinated people were more likely to contract COVID-19. One study showed the risk of “breakthrough” infection was significantly higher among people who were boosted and that more vaccinations resulted in a greater risk of COVID-19. A second study showed adults who were not “up-to-date” with their shots had a 23% lower incidence of COVID-19 than their “up-to-date” colleagues. 3. The trials underestimated the adverse events, including death, despite evidence in the data. Harms were also underreported and underestimated for a number of reasons, according to the authors, a practice that tends to be common in randomized industry-sponsored vaccine trials in general and “exceptionally evident” here. First, because Pfizer unblinded the trial within just a few weeks of the emergency use authorization and allowed people in the placebo group to take the vaccine, there was not sufficient time to identify late-occurring harms because there was no longer a control group. “Was this necessary, given that none of the deaths in the Pfizer trial were attributed to COVID-19 as the primary cause, and given the very low IFR [infection fatality rate] for a relatively healthy population?” they asked. Also, trial coordinators were “haphazard” in their approach to monitoring AEs. They prioritized documenting events thought to be related to COVID-19 rather than to the vaccines for the first seven days and only recorded “unsolicited” AEs for 30-60 days. After that period, even very SAEs, like death, were not recorded. Even for the AEs recorded in the first seven days, they only solicited data from 20% of the population. None of the trial data was independently verified. “Such secrecy may have enabled the industry to more easily present an inflated and distorted estimate of the genetic injections’ benefits, along with a gross underestimation of potential harms,” they wrote. Subsequent analysis by Michels et al. revealed that deaths and other SAEs — like life-threatening conditions, inpatient hospitalization or extension of hospitalization, persistent or significant disability/incapacity, a congenital anomaly, or a medically significant event — did occur after the cutoff period and before the FDA advisory meeting where emergency authorization was recommended. During the first 33 weeks of the Pfizer trials, 38 subjects died, according to Pfizer’s own data, although independent research by Michels et al. estimated that that number is only approximately 17% of the actual projected number due to missing data. And after that, the rate of deaths continued to increase. Michaels et al. found Pfizer failed to report a substantial increase in the number of deaths due to cardiovascular events. They also found a consistent pattern of reporting delays on the date of the death on subjects’ case reports. Overall, the review authors reported that there were “twice as many cardiac deaths proportionately among vaccinated compared to unvaccinated subjects in the Pfizer trials.” In their discussion, the authors wrote “Based on the extended Pfizer trial findings, our person-years estimate yielded a 31% increase in overall mortality among vaccine recipients, a clear trend in the wrong direction.” This raises serious red flags about how the registrational trials were conducted, Mead said. “Assessments of the safety profile of the COVID-19 modified mRNA injections warrant an objective precautionary perspective, any substantial upward trend in all cause mortality within the intervention arm of the trial population reflects badly on the intervention.” 4. Numbers of SAEs in the trials and post-rollout reporting are well-documented, despite claims to the contrary. Both Pfizer and Moderna found about 125 SAEs per 100,000 vaccine recipients, or one SAE for every 800 vaccines. However, because the trials excluded more vulnerable people, the authors note, even higher proportions of SAEs would be expected in the general population. The Fraiman et al. reanalysis of the Pfizer trial data found a significant 36% higher risk of SAEs, which included deaths and many life-threatening conditions in the vaccinated participants. Official SAEs for other vaccines average around only 1-2 per million. Fraiman et alestimated 1,250 SEAs per million vaccines, exceeding that benchmark by “at least 600-fold.” After the vaccine rollout, analyses of two large drug safety reporting systems in the U.S. and Europe identified signals for myocardial infarction, pulmonary embolism, cardio-respiratory arrest, cerebral infarction, and cerebral hemorrhage associated with both mRNA vaccines, along with ischemic stroke. And millions of AEs have been reported to those systems. Another study by Skidmore et al. estimated the total number of fatalities from the vaccines in 2021 alone was 289,789. Autopsy studies have also provided additional evidence of serious harms, including evidence that most COVID-19 mRNA vaccine-related deaths resulted from injury to the cardiovascular system. In multiple autopsy studies, German pathologist Aren Burkhardt documented the presence of vaccine-mRNA-produced spike proteins in blood vessel walls and brain tissues. This research helps to explain documented vaccine-induced toxicities affecting the nervous, immune, reproductive and other systems. The Pfizer data also showed an overwhelming number of adverse effects. According to a confidential document released in August 2022, Pfizer had documented approximately 1.6 million AEs affecting nearly every organ system, and one-third of them were classified as serious. In Pfizer’s trial, Michels and colleagues found a nearly 4-fold increase (OR 3.7, 95%CI 1.02-13.2, p = 0.03) in serious cardiac events (e.g., heart attack, acute coronary syndrome) in the vaccine group. Neither the original trial report nor Pfizer’s Summary Clinical Safety report acknowledged or commented on this safety signal. “The serious adverse events are all well documented,” Mead said. “Yet it’s surprising to see so many in the medical field continue to ignore or dismiss outright the latter half of the equation when considering all cause mortality trends.” 5. The failure to appropriately test for safety and toxicity poses serious problems. Researchers have raised concerns that the mRNA technology is inherently unstable and difficult to store, which leads to batch variability and contamination linked to different rates of AEs. Recent findings by McKernan et al. that found Pfizers’ mRNA vaccines are contaminated with plasmid DNA that shouldn’t be present — and wasn’t present in the vaccines used in the trials – raising serious safety issues. That’s because “Process 1,” used in the trials to generate the vaccines involved in vitro transcription of synthetic DNA — essentially a “clean” process. However, that process isn’t viable for mass production, so the manufacturers used “Process 2,” which involves using E. coli bacteria to replicate the plasmids. Removing plasmids E coli. can result in residual plasmids in the vaccines and the effects of their presence is unknown. McKernan’s work also revealed the presence of DNA from simian virus 40 (SV40), an oncogenic DNA virus originally isolated in 1960 from contaminated polio vaccines, induces lymphomas, brain tumors, and other malignancies in laboratory animals, raising other safety concerns. Researchers from Cambridge published a paper in Nature in December 2023, where they found an inherent defect in the modified RNA instructions for the spike protein in COVID-19 immunizations that causes the machinery that translates the gene to the spike protein to “slip” about 10% of the time This process creates “frameshifts” that cause cells to produce “off-target” proteins in addition to the spike. These proteins, which developers either failed to look for or did not report to regulators, cause undesirable immune responses whose long-term effects are unknown. 6. There are many different possible biological mechanisms that cause AEs and vaccine ineffectiveness. The review points readers to a series of papers that explain a number of different theories to explain the high number of AEs from the COVID-19 mRNA vaccines. “The mechanisms of molecular mimicry, antigen cross-reactivity, pathogenic priming, viral reactivation, immune exhaustion, and other factors related to immune dysfunction all reinforce the biological plausibility for vaccine-induced pathogenesis of malignant and autoimmune diseases,” they wrote. And these mechanisms of immune activation are distinct from the body’s response to a viral infection. They also note the toxic effects of the primary adjuvant, PEG, and of the spike protein itself. They close their analysis of the vaccines with a complex explanation for the different immunological basis for protection provided by the vaccines versus natural immunity through infection. They explain the mechanisms for vaccine failure and problems generated by the ability for the mRNA vaccines to perpetuate the emergence of new variants. https://childrenshealthdefense.org/defender/scientists-global-moratorium-mrna-vaccines-removal-childhood-schedule/ https://donshafi911.blogspot.com/2024/01/scientists-call-for-global-moratorium.html
    CHILDRENSHEALTHDEFENSE.ORG
    Scientists Call for Global Moratorium on mRNA Vaccines, Immediate Removal From Childhood Schedule
    A review paper published last week in the journal Cureus is the first peer-reviewed paper to call for a global moratorium on the COVID-19 mRNA vaccines. The authors say that reanalyzed data from the vaccine makers’ trials and high rates of serious post-injection injuries indicate the mRNA gene therapy vaccines should not have been authorized for use.
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  • USING YOUR MENTAL ENERGY
    PART 117

    In other words, this #universal power takes its creative direction from the #word you give it.

    Once man realizes this great #truth, it becomes the most important of all his considerations with what character this sensitive reproductive #power is invested.

    It’s the unvarying #law of this #CreativeLife #principle that as a man #thinks in his #heart, so is he.
    🧠USING YOUR MENTAL ENERGY ✅PART 117 In other words, this #universal power takes its creative direction from the #word you give it. Once man realizes this great #truth, it becomes the most important of all his considerations with what character this sensitive reproductive #power is invested. It’s the unvarying #law of this #CreativeLife #principle that as a man #thinks in his #heart, so is he.
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  • Researchers urge governments to endorse a global moratorium on mRNA injections in a newly released science paper
    Rhoda WilsonJanuary 26, 2024
    In a paper published on Wednesday, researchers re-analysed the Pfizer covid “vaccine” phase 3 trial data and found more serious adverse events among those in the vaccine group.

    This is not what published reports from Pfizer’s phase 3 trials said. “Many key trial findings were either misreported or omitted entirely from published reports,” the researchers said.

    Seven researchers – M. Nathaniel Mead, Stephanie Seneff, Russ Wolfinger, Jessica Rose, Kris Denhaerynck, Steve Kirsch and Peter A. McCullough – set out to re-analyse Pfizer’s trial data because:

    our understanding of covid vaccinations and their impact on health and mortality has evolved substantially since the first vaccine rollouts; and,
    problems with the methods, execution, and reporting of the pivotal phase 3 trials have emerged.
    On Wednesday, they published their findings in a peer-reviewed paper titled ‘Covid-19 mRNA Vaccines: Lessons Learned from the Registrational Trials and Global Vaccination Campaign’. The paper was published in Cureus, a journal of medical science.

    “Re-analysis of the Pfizer trial data identified statistically significant increases in serious adverse events (SAEs) in the vaccine group,” the researchers wrote.

    Adding, “Numerous SAEs were identified following the Emergency Use Authorisation (EUA), including death, cancer, cardiac events, and various autoimmune, haematological, reproductive, and neurological disorders.”

    The EUA the researchers are referring to is the authorisation granted to Pfizer by the US Food and Drugs Administration (“FDA”).

    As the paper noted, Pfizer’s covid “vaccines” never underwent adequate safety and toxicological testing according to previously established scientific standards. It goes on to detail the absolute risk reduction, the underreporting of harms during trials, the shifting narratives and illusions of protection, quality control and manufacturing process-related impurities, the biological mechanisms underlying adverse events (“AEs”) and why, based on how our immune systems work, the vaccine is ineffective.

    Concluding their comprehensive review, the researchers wrote:

    Given the extensive, well-documented SAEs and unacceptably high harm-to-reward ratio, we urge governments to endorse a global moratorium on the modified mRNA products until all relevant questions pertaining to causality, residual DNA, and aberrant protein production are answered.

    Mead M, Seneff S, Wolfinger R, et al. (January 24, 2024) COVID-19 mRNA Vaccines: Lessons Learned from the Registrational Trials and Global Vaccination Campaign. Cureus 16(1): e52876. doi:10.7759/cureus.52876none
    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 paper noted that the gene therapy products (“GTPs”) vaccine platform has been studied for over 30 years as an experimental cancer treatment, with the terms “gene therapy” and “mRNA vaccination” often used interchangeably.

    “Although we employ the terms ‘vaccine’ and ‘vaccination’ throughout this paper, the covid-19 mRNA products are also accurately termed gene therapy products (GTPs) because, in essence, this was a case of GTP technology being applied to vaccination,” they wrote.

    As such, throughout their analysis, the terms “vaccines” and “vaccinations” are used interchangeably with injections, inoculations, biologicals, or simply, products.

    The following are some excerpts from the paper. You can read the full paper HERE.

    Serious Harms Revealed after EUA was Granted

    In this narrative review, we revisit the registrational trials and review analyses of the AEs from these trials and other relevant studies. Most of the revelations have only recently come to light, due to the past few years of extensive censorship of healthcare professionals and research scientists who challenged the prevailing narrative set forth by the vaccine enterprise.

    Despite the rhetoric, no large randomised double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalisation or death.

    The study designs for the pivotal trials that led to the EUA were never intended to determine whether the mRNA inoculations could help prevent severe disease or premature death.

    It was only after the EUA that the serious biological consequences of rushing the trials became evident, with numerous cardiovascular, neurological, reproductive, haematological, malignant, and autoimmune SAEs identified and published in the peer-reviewed medical literature.

    Moreover, the covid mRNA vaccines produced via Process 1 and evaluated in the trials were not the same products eventually distributed worldwide; all of the covid-19 mRNA products released to the public were produced via Process 2 and have been shown to have varying degrees of DNA contamination.

    The process-related impurities were absent from the covid-19 mRNA products used in the registrational trials. Virtually all doses used in those trials originated from “clinical batches” produced using what is known as Process 1. As a post-authorisation emergency supply measure for global distribution, however, a method much more suitable for mass production known as Process 2 was devised utilising bacterial plasmid DNA.

    The failure of regulatory authorities to heretofore disclose process-related impurities (e.g., SV40) has further increased concerns regarding safety and quality control oversight of mRNA vaccine manufacturing processes.

    Incentives Played a Key Role in Undermining Scientific Evaluation

    Political and financial incentives may have played a key role in undermining the scientific evaluation process leading up to the EUA.

    Before the pandemic, the US National Institutes of Health invested $116 million (35%) in mRNA vaccine technology, the Biomedical Advanced Research and Development Authority (“BARDA”) had invested $148 million (44%), while the Department of Defence (“DOD”) contributed $72 million (21%) to mRNA vaccine development.

    BARDA and the DOD also collaborated closely in the co-development of Moderna’s mRNA vaccine, dedicating over $18 billion, which included guaranteed vaccine purchases. This entailed pre-purchasing hundreds of millions of mRNA vaccine doses, alongside direct financial support for the clinical trials and the expansion of Moderna’s manufacturing capabilities.

    Once the pandemic began, $29.2 billion – 92% of which came from US public funds – was dedicated to the purchase of covid-19 mRNA products; another $2.2 billion (7%) was channelled into supporting clinical trials, and $108 million (less than 1%) was allocated for manufacturing and basic research.

    Using US taxpayer money to purchase so many doses in advance would suggest that, before the EUA process, US federal agencies were strongly biased toward successful outcomes for the registrational trials.

    Established Vaccine Testing Period Abolished

    Before the rapid authorisation process, no vaccine had been permitted for market release without undergoing a testing period of at least four years. Previous timeframes for phase 3 trial testing averaged 10 years. Health departments have stated that 10-15 years is the normal timeframe for evaluating vaccine safety.

    The previously established 10-15-year timeframe for clinical evaluation of vaccines was deemed necessary to ensure adequate time for monitoring the development of AEs such as cancers and autoimmune disorders.

    Pfizer’s covid vaccine completed the process in seven months.

    Established Safety Standards Abolished

    With the covid vaccines, safety was never assessed in a manner commensurate with previously established scientific standards, as numerous safety testing and toxicology protocols typically followed by the FDA were sidestepped.

    Historical accounts bear witness to instances where vaccines were prematurely introduced to the market under immense pressure, only to reveal disabling or even fatal AEs later on. Examples include the 1955 contamination of polio vaccines, instances of Guillain-Barré syndrome observed in flu vaccine recipients in 1976, and the connection between narcolepsy and a specific flu vaccine in 2009.

    Against this backdrop, it is not surprising that so many medical and public health experts voiced concerns about covid mRNA vaccines bypassing the normal safety testing process.

    Concerns about inadequate safety testing extend beyond the usual regulatory approval standards and practices.

    As there were no specific regulations at the time of the rapid approval process, regulatory agencies quickly “adapted” the products, generalised the definition of “vaccine” to accommodate them, and then authorised them for EUA for the first time ever against a viral disease.

    Due to the GTPs’ reclassification as vaccines, none of their components have been thoroughly evaluated for safety. The main concern, in a nutshell, is that the covid mRNA products may transform body cells into viral protein factories that have no off-switch – i.e., no built-in mechanism to stop or regulate such proliferation – with the spike protein (“S-protein”) being generated for prolonged periods, causing chronic, systemic inflammation and immune dysfunction.

    When the S-protein enters the bloodstream and disseminates systemically, it may become a contributing factor to diverse AEs in susceptible people.

    Enforce a Global Moratorium

    Given the well-documented SAEs and unacceptable harm-to-reward ratio, we urge governments to endorse and enforce a global moratorium on these modified mRNA products until all relevant questions pertaining to causality, residual DNA, and aberrant protein production are answered.



    https://expose-news.com/2024/01/26/researchers-urge-a-global-moratorium-on-mrna/
    Researchers urge governments to endorse a global moratorium on mRNA injections in a newly released science paper Rhoda WilsonJanuary 26, 2024 In a paper published on Wednesday, researchers re-analysed the Pfizer covid “vaccine” phase 3 trial data and found more serious adverse events among those in the vaccine group. This is not what published reports from Pfizer’s phase 3 trials said. “Many key trial findings were either misreported or omitted entirely from published reports,” the researchers said. Seven researchers – M. Nathaniel Mead, Stephanie Seneff, Russ Wolfinger, Jessica Rose, Kris Denhaerynck, Steve Kirsch and Peter A. McCullough – set out to re-analyse Pfizer’s trial data because: our understanding of covid vaccinations and their impact on health and mortality has evolved substantially since the first vaccine rollouts; and, problems with the methods, execution, and reporting of the pivotal phase 3 trials have emerged. On Wednesday, they published their findings in a peer-reviewed paper titled ‘Covid-19 mRNA Vaccines: Lessons Learned from the Registrational Trials and Global Vaccination Campaign’. The paper was published in Cureus, a journal of medical science. “Re-analysis of the Pfizer trial data identified statistically significant increases in serious adverse events (SAEs) in the vaccine group,” the researchers wrote. Adding, “Numerous SAEs were identified following the Emergency Use Authorisation (EUA), including death, cancer, cardiac events, and various autoimmune, haematological, reproductive, and neurological disorders.” The EUA the researchers are referring to is the authorisation granted to Pfizer by the US Food and Drugs Administration (“FDA”). As the paper noted, Pfizer’s covid “vaccines” never underwent adequate safety and toxicological testing according to previously established scientific standards. It goes on to detail the absolute risk reduction, the underreporting of harms during trials, the shifting narratives and illusions of protection, quality control and manufacturing process-related impurities, the biological mechanisms underlying adverse events (“AEs”) and why, based on how our immune systems work, the vaccine is ineffective. Concluding their comprehensive review, the researchers wrote: Given the extensive, well-documented SAEs and unacceptably high harm-to-reward ratio, we urge governments to endorse a global moratorium on the modified mRNA products until all relevant questions pertaining to causality, residual DNA, and aberrant protein production are answered. Mead M, Seneff S, Wolfinger R, et al. (January 24, 2024) COVID-19 mRNA Vaccines: Lessons Learned from the Registrational Trials and Global Vaccination Campaign. Cureus 16(1): e52876. doi:10.7759/cureus.52876none 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 paper noted that the gene therapy products (“GTPs”) vaccine platform has been studied for over 30 years as an experimental cancer treatment, with the terms “gene therapy” and “mRNA vaccination” often used interchangeably. “Although we employ the terms ‘vaccine’ and ‘vaccination’ throughout this paper, the covid-19 mRNA products are also accurately termed gene therapy products (GTPs) because, in essence, this was a case of GTP technology being applied to vaccination,” they wrote. As such, throughout their analysis, the terms “vaccines” and “vaccinations” are used interchangeably with injections, inoculations, biologicals, or simply, products. The following are some excerpts from the paper. You can read the full paper HERE. Serious Harms Revealed after EUA was Granted In this narrative review, we revisit the registrational trials and review analyses of the AEs from these trials and other relevant studies. Most of the revelations have only recently come to light, due to the past few years of extensive censorship of healthcare professionals and research scientists who challenged the prevailing narrative set forth by the vaccine enterprise. Despite the rhetoric, no large randomised double-blind placebo-controlled trials have ever demonstrated reductions in SARS-CoV-2 transmission, hospitalisation or death. The study designs for the pivotal trials that led to the EUA were never intended to determine whether the mRNA inoculations could help prevent severe disease or premature death. It was only after the EUA that the serious biological consequences of rushing the trials became evident, with numerous cardiovascular, neurological, reproductive, haematological, malignant, and autoimmune SAEs identified and published in the peer-reviewed medical literature. Moreover, the covid mRNA vaccines produced via Process 1 and evaluated in the trials were not the same products eventually distributed worldwide; all of the covid-19 mRNA products released to the public were produced via Process 2 and have been shown to have varying degrees of DNA contamination. The process-related impurities were absent from the covid-19 mRNA products used in the registrational trials. Virtually all doses used in those trials originated from “clinical batches” produced using what is known as Process 1. As a post-authorisation emergency supply measure for global distribution, however, a method much more suitable for mass production known as Process 2 was devised utilising bacterial plasmid DNA. The failure of regulatory authorities to heretofore disclose process-related impurities (e.g., SV40) has further increased concerns regarding safety and quality control oversight of mRNA vaccine manufacturing processes. Incentives Played a Key Role in Undermining Scientific Evaluation Political and financial incentives may have played a key role in undermining the scientific evaluation process leading up to the EUA. Before the pandemic, the US National Institutes of Health invested $116 million (35%) in mRNA vaccine technology, the Biomedical Advanced Research and Development Authority (“BARDA”) had invested $148 million (44%), while the Department of Defence (“DOD”) contributed $72 million (21%) to mRNA vaccine development. BARDA and the DOD also collaborated closely in the co-development of Moderna’s mRNA vaccine, dedicating over $18 billion, which included guaranteed vaccine purchases. This entailed pre-purchasing hundreds of millions of mRNA vaccine doses, alongside direct financial support for the clinical trials and the expansion of Moderna’s manufacturing capabilities. Once the pandemic began, $29.2 billion – 92% of which came from US public funds – was dedicated to the purchase of covid-19 mRNA products; another $2.2 billion (7%) was channelled into supporting clinical trials, and $108 million (less than 1%) was allocated for manufacturing and basic research. Using US taxpayer money to purchase so many doses in advance would suggest that, before the EUA process, US federal agencies were strongly biased toward successful outcomes for the registrational trials. Established Vaccine Testing Period Abolished Before the rapid authorisation process, no vaccine had been permitted for market release without undergoing a testing period of at least four years. Previous timeframes for phase 3 trial testing averaged 10 years. Health departments have stated that 10-15 years is the normal timeframe for evaluating vaccine safety. The previously established 10-15-year timeframe for clinical evaluation of vaccines was deemed necessary to ensure adequate time for monitoring the development of AEs such as cancers and autoimmune disorders. Pfizer’s covid vaccine completed the process in seven months. Established Safety Standards Abolished With the covid vaccines, safety was never assessed in a manner commensurate with previously established scientific standards, as numerous safety testing and toxicology protocols typically followed by the FDA were sidestepped. Historical accounts bear witness to instances where vaccines were prematurely introduced to the market under immense pressure, only to reveal disabling or even fatal AEs later on. Examples include the 1955 contamination of polio vaccines, instances of Guillain-Barré syndrome observed in flu vaccine recipients in 1976, and the connection between narcolepsy and a specific flu vaccine in 2009. Against this backdrop, it is not surprising that so many medical and public health experts voiced concerns about covid mRNA vaccines bypassing the normal safety testing process. Concerns about inadequate safety testing extend beyond the usual regulatory approval standards and practices. As there were no specific regulations at the time of the rapid approval process, regulatory agencies quickly “adapted” the products, generalised the definition of “vaccine” to accommodate them, and then authorised them for EUA for the first time ever against a viral disease. Due to the GTPs’ reclassification as vaccines, none of their components have been thoroughly evaluated for safety. The main concern, in a nutshell, is that the covid mRNA products may transform body cells into viral protein factories that have no off-switch – i.e., no built-in mechanism to stop or regulate such proliferation – with the spike protein (“S-protein”) being generated for prolonged periods, causing chronic, systemic inflammation and immune dysfunction. When the S-protein enters the bloodstream and disseminates systemically, it may become a contributing factor to diverse AEs in susceptible people. Enforce a Global Moratorium Given the well-documented SAEs and unacceptable harm-to-reward ratio, we urge governments to endorse and enforce a global moratorium on these modified mRNA products until all relevant questions pertaining to causality, residual DNA, and aberrant protein production are answered. https://expose-news.com/2024/01/26/researchers-urge-a-global-moratorium-on-mrna/
    EXPOSE-NEWS.COM
    Researchers urge governments to endorse a global moratorium on mRNA injections in a newly released science paper
    In a paper published on Wednesday, researchers re-analysed the Pfizer covid “vaccine” phase 3 trial data and found more serious adverse events among those in the vaccine group. This is not what pub…
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  • ‘Operation Al-Aqsa Flood’ Day 113: A day after ICJ ruling, U.S. and allies withdraw funding to UNRWA
    At least five countries have pulled their funding from the U.N. agency for Palestinian refugees over Israeli claims that staff members participated in the October 7 attack. Israel keeps killing Palestinians in Gaza and the West Bank.

    Mondoweiss Palestine BureauJanuary 27, 2024
    A grief-stricken Palestinian man holds up the shrouded body of a dead child in Gaza amidst a crowd outside the mortuary of the Al-Aqsa Hospital in central Gaza.
    Palestinians who lost their loved ones mourn as bodies of the deceased are taken out of the mortuary of Al-Aqsa Hospital for burial in Dair El-Balah, Gaza on January 26, 2024. (Omar Ashtawy/apaimages)
    Casualties:

    26,257 killed* and at least 64,797 wounded in the Gaza Strip.
    387+ Palestinians killed in the occupied West Bank and East Jerusalem
    Israel revises its estimated October 7 death toll down from 1,400 to 1,147.
    556 Israeli soldiers killed since October 7, and at least 3,221 injured.**
    *This figure was confirmed by Gaza’s Ministry of Health on Saturday, January 27. Some rights groups put the death toll number at more than 33,000 when accounting for those presumed dead.

    ** This figure is released by the Israeli military.

    Key Developments

    International Court of Justice ruling on Friday garners mixed reviews, Israel and U.S. maintain Israeli innocence, Palestinians point out nothing short of ceasefire will end genocide.
    UNRWA fires 12 members of staff and announces launch of independent investigation following Israeli claims that some UNRWA employees participated in October 7 attack.
    U.S., UK, Australia, Italy, and Canada pull funding from UNRWA without waiting for the results of investigation, despite dire humanitarian need in occupied Palestinian territories amid relentless Israeli assault on Gaza.
    Israeli forces kill at least 174 Palestinians, injure 310 others in Gaza in 24 hours.
    Multiple reports emerge of Israeli forces killing Palestinians waving white flags, including two brothers aged 14 and 20 fleeing Khan Younis.
    Israeli forces kill Palestinian in northern occupied West Bank overnight, detain at least eight others.
    U.S. federal court case opens accusing President Joe Biden and other key officials of complicity in Israeli violations against Palestinians.
    Israeli strikes in southern Lebanon kill at least four members of Hezbollah movement.
    U.S. carries out new strikes in Yemen after Ansar Allah targets tanker in Red Sea.
    World reacts to ICJ ruling

    The International Court of Justice (ICJ) ruling on Friday — which found that there was plausible evidence of Israel committing genocidal acts in Gaza and ordered that Israel show proof within a month that it was reversing course on its indiscriminate targeting of civilians in Gaza and obstruction of humanitarian aid, but stopped short of calling for a ceasefire — has sparked reactions from Israel, Palestine, and across the world.

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    Some of the Israeli press framed the decision not to order an immediate ceasefire as a “win” and the “best Israel could hope for.” Others interpreted it as a “warning shot” that could further isolate the Israeli government and its closest ally, the United States, on the international stage.

    While Israel had vowed ahead of the ruling that it wouldn’t comply with any ICJ calls for an end to the relentless assault on Gaza, analysts in Israel believe that Tel Aviv won’t openly reject the provisional orders issued by the court — as the Israeli government continues to argue, despite extensive evidence to the contrary on the ground, that it is already doing its utmost to protect Palestinian civilians.

    The ICJ notably ordered that Israel prevent and punish officials inciting to genocide. South Africa, which presented the case in front of the ICJ, had cited statements from high-ranking members of the Israeli government, including Prime Minister Benjamin Netanyahu, as proof of genocidal intent against Palestinians in its oral arguments.

    The Times of Israel reported on Friday that Netanyahu had instructed his cabinet members to refrain from responding to the ICJ ruling, in vain. Far-right settler and National Security Minister Itamar Ben-Gvir, whose own words were cited in the court as evidence of genocidal intent, accused the ICJ of “not seek[ing] justice, but rather the persecution of Jewish people.”

    Netanyahu himself expressed anger that the court did not throw out the case in its entirety. “The court’s willingness to discuss this at all is a mark of disgrace that will not be erased for generations,” he said on Friday.

    In Palestine, Friday’s ruling received a mixed reception for entirely different reasons.

    Hamas politburo member Izzat al-Rishq welcomed the decision as “an important step towards justice for our people.” Meanwhile, Palestinian Authority Prime Minister Mohammed Shtayyeh said the ruling marked an “end to Israel’s era of impunity.” The PA Foreign Ministry meanwhile said an immediate ceasefire was the only way to ensure Israel’s compliance with the court orders.

    South Africa, which has been hailed for bringing the case to the court, commended the ICJ.

    “South Africa had to do what was possible to protect hundreds of thousands of Palestinians and not stand idly by. It must do everything possible to protect hundreds of thousands of Palestinians,” South African Foreign Minister Naledi Pandor said on Friday. “Israel cannot continue its crimes against Palestinian civilians without consequences.”

    Scores of countries around the world also expressed support for the decision, with the European Union saying it expected its “full, immediate and effective implementation.”

    Israel’s staunchest allies, however, continued to maintain that the court case was baseless.

    “There’s no indication that we’ve seen that validates a claim of genocidal intent or action by the Israeli Defense Forces,” U.S. National Security Council spokesman John Kirby told journalists on Friday, adding that he stood by his previous statements that the ICJ case was “meritless, counterproductive, and completely without any basis in fact whatsoever.”

    In the U.K., a spokesperson for the U.K.’s Foreign, Commonwealth and Development Office told Al Jazeera on Saturday: “Our view is that Israel’s actions in Gaza cannot be described as a genocide, which is why we thought South Africa’s decision to bring the case was wrong and provocative.”

    These statements likely ring hollow for Palestinians in Gaza, many of whom had hoped that the ICJ would call for an immediate ceasefire that could put an end to the devastation and misery they have been facing for 113 days.

    “We have no one to support us. No one can stop Israel, no court decisions or UN resolutions. As long as the U.S. supports Israel, we will continue to suffer,” Hassan Khalil, who has been internally displaced five times in three months, told Al Jazeera.

    For Palestinian rights groups and advocates, the onus is now on the international community to abide by the ruling and the Geneva Convention, and bring an end to the slaughter of Palestinians.

    “This ruling holds immense significance, serving as a crucial milestone in the collective effort to hold Israel accountable for the egregious crimes committed against the Palestinian people,” Issam Younis, the general director of the Al-Mezan Center for Human Rights, said. “The responsibility to end the ongoing genocide in Gaza now lies with the international community, which must fulfill its legal obligations and take decisive measures to safeguard Palestinians from the genocidal acts perpetrated by Israel. Ending the ongoing genocidal Israeli military campaign in Gaza should be the primary pursuit.”

    Gaza suffering doesn’t end

    As expected, the events in The Hague have not slowed Israel’s war machine in the Gaza Strip.

    Fighting between armed Palestinian groups and Israeli ground forces was reported in the past 24 hours in al-Bureij, Khan Younis, al-Maghazi, Shuja’iyya, al-Masdar, Beit Lahia, and east of Rafah.

    The Gaza Ministry of Health reported on Saturday that Israeli forces had killed at least 174 Palestinians and injured 310 others in the span of 24 hours – bringing the overall estimated toll, which does not include thousands of people still trapped under the rubble, to 26,257 killed and 64,797 wounded.

    WAFA news agency reported deadly Israeli strikes on tents and homes where displaced people have been sheltering in the horrifically crowded Rafah, as well as in Khan Younis, Deir al-Balah, and Gaza City. The Palestinian Red Crescent Society meanwhile reported that Al-Amal Hospital in Khan Younis continued to be under siege by Israeli forces, which shot and killed a young man who had taken refuge in the hospital courtyard on Saturday.

    Euro-Med Human Rights Monitor reported on Friday on the killing of two brothers by Israeli snipers earlier this week as they tried to evacuate Al-Amal Hospital — the latest of numerous alleged cases of deliberate and indiscriminate killing of Palestinian civilians by Israeli forces in Gaza.

    Fourteen-year-old Nahed Barbakh, who eyewitnesses said was holding a white flag, was shot by Israeli snipers three times and killed. His brother Ramez, 20, was also shot in the head while trying to rescue the boy.

    On Friday, the Office of the United Nations High Commissioner for Human Rights (OHCHR) slammed Israel’s relentless mass displacement of some 85 percent of Gaza’s population into ever tinier slivers of land while continuing to bomb them wherever they go.

    “I have very grave concerns that these chaotic and mass evacuation orders are ineffective in ensuring the safety of Palestinian civilians, instead placing them in increasingly vulnerable, dangerous, situations,” Ajith Sunghay, OHCHR’s director in the occupied Palestinian territories. “Such a failure violates Israel’s obligations under international law.”

    A report by Ground Truth Solutions, which interviewed scores of internally displaced Palestinians in recent months, said “very few people” in Gaza were able to access formal humanitarian aid amid breakdowns in communication and difficulties in access, leaving many to rely only on one another.

    “People are sharing resources among themselves. Their primary source of support is family members. People have also been both giving and receiving food, water, shelter, electricity and healthcare independently of the aid system. They have been taking care of other people’s children, and relying on community support for transportation and the management of daily tasks like sourcing meals, finding fuel, organizing shelters and so on,” the report noted.

    UNRWA once again in the crosshairs

    On the very day that the ICJ ordered for Israel to ensure the unimpeded entry of humanitarian aid into Gaza, Washington saw fit to cut off all funding to UNRWA, the United Nations agency for Palestinian refugees.

    The decision came after Israel claimed that 12 UNRWA workers had been involved in the October 7 attack. UNRWA has said that it has terminated the contracts of these workers as it commissions an independent investigation into the allegations — but the United Kingdom, Australia, Italy, and Canada have followed the U.S.’s lead and pulled their funding of the organization.

    In an election year during which he is trying to convince the American public that he is the only alternative to the return of Donald Trump to the White House, U.S. President Joe Biden is following his predecessor’s lead, as Trump had partially suspended funding to UNRWA in 2018.

    “We call on the countries that announced the cessation of their support for UNRWA to immediately reverse their decision, which entails great political and humanitarian relief risks, as at this particular time and in light of the continuing aggression against the Palestinian people, we need the maximum support for this international organization and not stopping support and assistance to it,” Palestine Liberation Organization Secretary-General Hussein al-Sheikh wrote on X.

    Hamas, meanwhile, called on the United Nations “not to yield to the threats and blackmails.”

    “We stress the importance of the role of these agencies in providing relief to our people and documenting the crimes of the occupation, which exceed the most horrific crimes known to humanity in our modern era,” the movement said in a statement.

    Even as the U.S. appears steadfast in siding with Israel, Biden is facing legal trouble at home over his administration’s failure to stop the ongoing genocide in Gaza.

    Palestinians testified on Friday in front of a federal court, in a case brought forth by the Center for Constitutional Rights (CCR) against Biden, Secretary of State Antony Blinken, and Defense Secretary Lloyd Austin, arguing that the three high-ranking officials are liable under U.S. law for complicity in Israel’s violations of the Genocide Convention.

    Israeli forces kill Palestinian in the West Bank, exchanges of fire continue on all fronts

    In the occupied West Bank, Israeli forces killed at least one Palestinian overnight.

    Qassam Ahmad Yasin, 27, was shot and killed in the village of Deir Abu Deif near Jenin, where overnight clashes were reported between Israeli forces and Palestinian residents. Armed confrontations were also reported in Qalqilya, near the illegal Israeli settlement of Etzion, and an Israeli checkpoint in Beit Furik.

    Israeli forces have been setting up more flying checkpoints across the Jenin governorate in recent days, assaulting Palestinians and tearing down flags.

    Israeli forces detained at least eight Palestinians overnight across the West Bank, WAFA reported.

    Meanwhile, Friday marked the sixteenth consecutive week of Israeli restrictions for worshippers seeking to pray at the Al-Aqsa Mosque in occupied East Jerusalem. Israeli forces fired tear gas and skunk water at Palestinians seeking to enter the holy site on the Muslim day of worship.

    Further north, the Hezbollah movement said an Israeli airstrike on the southern Lebanese village of Beit Lif on Friday night had killed four of its members, as the Lebanese resistance movement continues to exchange fire with Israel across the Blue Line.

    Yemen’s Houthi rebels meanwhile struck a British-linked tanker in the Gulf of Aden on Friday. U.S. forces launched an airstrike on Hodeidah on Saturday in retaliation.

    BEFORE YOU GO – At Mondoweiss, we understand the power of telling Palestinian stories. For 17 years, we have pushed back when the mainstream media published lies or echoed politicians’ hateful rhetoric. Now, Palestinian voices are more important than ever.

    Our traffic has increased ten times since October 7, and we need your help to cover our increased expenses.

    Support our journalists with a donation today.

    https://mondoweiss.net/2024/01/operation-al-aqsa-flood-day-113-a-day-after-icj-ruling-u-s-and-allies-withdraw-funding-to-unrwa/
    ‘Operation Al-Aqsa Flood’ Day 113: A day after ICJ ruling, U.S. and allies withdraw funding to UNRWA At least five countries have pulled their funding from the U.N. agency for Palestinian refugees over Israeli claims that staff members participated in the October 7 attack. Israel keeps killing Palestinians in Gaza and the West Bank. Mondoweiss Palestine BureauJanuary 27, 2024 A grief-stricken Palestinian man holds up the shrouded body of a dead child in Gaza amidst a crowd outside the mortuary of the Al-Aqsa Hospital in central Gaza. Palestinians who lost their loved ones mourn as bodies of the deceased are taken out of the mortuary of Al-Aqsa Hospital for burial in Dair El-Balah, Gaza on January 26, 2024. (Omar Ashtawy/apaimages) Casualties: 26,257 killed* and at least 64,797 wounded in the Gaza Strip. 387+ Palestinians killed in the occupied West Bank and East Jerusalem Israel revises its estimated October 7 death toll down from 1,400 to 1,147. 556 Israeli soldiers killed since October 7, and at least 3,221 injured.** *This figure was confirmed by Gaza’s Ministry of Health on Saturday, January 27. Some rights groups put the death toll number at more than 33,000 when accounting for those presumed dead. ** This figure is released by the Israeli military. Key Developments International Court of Justice ruling on Friday garners mixed reviews, Israel and U.S. maintain Israeli innocence, Palestinians point out nothing short of ceasefire will end genocide. UNRWA fires 12 members of staff and announces launch of independent investigation following Israeli claims that some UNRWA employees participated in October 7 attack. U.S., UK, Australia, Italy, and Canada pull funding from UNRWA without waiting for the results of investigation, despite dire humanitarian need in occupied Palestinian territories amid relentless Israeli assault on Gaza. Israeli forces kill at least 174 Palestinians, injure 310 others in Gaza in 24 hours. Multiple reports emerge of Israeli forces killing Palestinians waving white flags, including two brothers aged 14 and 20 fleeing Khan Younis. Israeli forces kill Palestinian in northern occupied West Bank overnight, detain at least eight others. U.S. federal court case opens accusing President Joe Biden and other key officials of complicity in Israeli violations against Palestinians. Israeli strikes in southern Lebanon kill at least four members of Hezbollah movement. U.S. carries out new strikes in Yemen after Ansar Allah targets tanker in Red Sea. World reacts to ICJ ruling The International Court of Justice (ICJ) ruling on Friday — which found that there was plausible evidence of Israel committing genocidal acts in Gaza and ordered that Israel show proof within a month that it was reversing course on its indiscriminate targeting of civilians in Gaza and obstruction of humanitarian aid, but stopped short of calling for a ceasefire — has sparked reactions from Israel, Palestine, and across the world. Advertisement Subscribe to the Mondoweiss YouTube Channel! Some of the Israeli press framed the decision not to order an immediate ceasefire as a “win” and the “best Israel could hope for.” Others interpreted it as a “warning shot” that could further isolate the Israeli government and its closest ally, the United States, on the international stage. While Israel had vowed ahead of the ruling that it wouldn’t comply with any ICJ calls for an end to the relentless assault on Gaza, analysts in Israel believe that Tel Aviv won’t openly reject the provisional orders issued by the court — as the Israeli government continues to argue, despite extensive evidence to the contrary on the ground, that it is already doing its utmost to protect Palestinian civilians. The ICJ notably ordered that Israel prevent and punish officials inciting to genocide. South Africa, which presented the case in front of the ICJ, had cited statements from high-ranking members of the Israeli government, including Prime Minister Benjamin Netanyahu, as proof of genocidal intent against Palestinians in its oral arguments. The Times of Israel reported on Friday that Netanyahu had instructed his cabinet members to refrain from responding to the ICJ ruling, in vain. Far-right settler and National Security Minister Itamar Ben-Gvir, whose own words were cited in the court as evidence of genocidal intent, accused the ICJ of “not seek[ing] justice, but rather the persecution of Jewish people.” Netanyahu himself expressed anger that the court did not throw out the case in its entirety. “The court’s willingness to discuss this at all is a mark of disgrace that will not be erased for generations,” he said on Friday. In Palestine, Friday’s ruling received a mixed reception for entirely different reasons. Hamas politburo member Izzat al-Rishq welcomed the decision as “an important step towards justice for our people.” Meanwhile, Palestinian Authority Prime Minister Mohammed Shtayyeh said the ruling marked an “end to Israel’s era of impunity.” The PA Foreign Ministry meanwhile said an immediate ceasefire was the only way to ensure Israel’s compliance with the court orders. South Africa, which has been hailed for bringing the case to the court, commended the ICJ. “South Africa had to do what was possible to protect hundreds of thousands of Palestinians and not stand idly by. It must do everything possible to protect hundreds of thousands of Palestinians,” South African Foreign Minister Naledi Pandor said on Friday. “Israel cannot continue its crimes against Palestinian civilians without consequences.” Scores of countries around the world also expressed support for the decision, with the European Union saying it expected its “full, immediate and effective implementation.” Israel’s staunchest allies, however, continued to maintain that the court case was baseless. “There’s no indication that we’ve seen that validates a claim of genocidal intent or action by the Israeli Defense Forces,” U.S. National Security Council spokesman John Kirby told journalists on Friday, adding that he stood by his previous statements that the ICJ case was “meritless, counterproductive, and completely without any basis in fact whatsoever.” In the U.K., a spokesperson for the U.K.’s Foreign, Commonwealth and Development Office told Al Jazeera on Saturday: “Our view is that Israel’s actions in Gaza cannot be described as a genocide, which is why we thought South Africa’s decision to bring the case was wrong and provocative.” These statements likely ring hollow for Palestinians in Gaza, many of whom had hoped that the ICJ would call for an immediate ceasefire that could put an end to the devastation and misery they have been facing for 113 days. “We have no one to support us. No one can stop Israel, no court decisions or UN resolutions. As long as the U.S. supports Israel, we will continue to suffer,” Hassan Khalil, who has been internally displaced five times in three months, told Al Jazeera. For Palestinian rights groups and advocates, the onus is now on the international community to abide by the ruling and the Geneva Convention, and bring an end to the slaughter of Palestinians. “This ruling holds immense significance, serving as a crucial milestone in the collective effort to hold Israel accountable for the egregious crimes committed against the Palestinian people,” Issam Younis, the general director of the Al-Mezan Center for Human Rights, said. “The responsibility to end the ongoing genocide in Gaza now lies with the international community, which must fulfill its legal obligations and take decisive measures to safeguard Palestinians from the genocidal acts perpetrated by Israel. Ending the ongoing genocidal Israeli military campaign in Gaza should be the primary pursuit.” Gaza suffering doesn’t end As expected, the events in The Hague have not slowed Israel’s war machine in the Gaza Strip. Fighting between armed Palestinian groups and Israeli ground forces was reported in the past 24 hours in al-Bureij, Khan Younis, al-Maghazi, Shuja’iyya, al-Masdar, Beit Lahia, and east of Rafah. The Gaza Ministry of Health reported on Saturday that Israeli forces had killed at least 174 Palestinians and injured 310 others in the span of 24 hours – bringing the overall estimated toll, which does not include thousands of people still trapped under the rubble, to 26,257 killed and 64,797 wounded. WAFA news agency reported deadly Israeli strikes on tents and homes where displaced people have been sheltering in the horrifically crowded Rafah, as well as in Khan Younis, Deir al-Balah, and Gaza City. The Palestinian Red Crescent Society meanwhile reported that Al-Amal Hospital in Khan Younis continued to be under siege by Israeli forces, which shot and killed a young man who had taken refuge in the hospital courtyard on Saturday. Euro-Med Human Rights Monitor reported on Friday on the killing of two brothers by Israeli snipers earlier this week as they tried to evacuate Al-Amal Hospital — the latest of numerous alleged cases of deliberate and indiscriminate killing of Palestinian civilians by Israeli forces in Gaza. Fourteen-year-old Nahed Barbakh, who eyewitnesses said was holding a white flag, was shot by Israeli snipers three times and killed. His brother Ramez, 20, was also shot in the head while trying to rescue the boy. On Friday, the Office of the United Nations High Commissioner for Human Rights (OHCHR) slammed Israel’s relentless mass displacement of some 85 percent of Gaza’s population into ever tinier slivers of land while continuing to bomb them wherever they go. “I have very grave concerns that these chaotic and mass evacuation orders are ineffective in ensuring the safety of Palestinian civilians, instead placing them in increasingly vulnerable, dangerous, situations,” Ajith Sunghay, OHCHR’s director in the occupied Palestinian territories. “Such a failure violates Israel’s obligations under international law.” A report by Ground Truth Solutions, which interviewed scores of internally displaced Palestinians in recent months, said “very few people” in Gaza were able to access formal humanitarian aid amid breakdowns in communication and difficulties in access, leaving many to rely only on one another. “People are sharing resources among themselves. Their primary source of support is family members. People have also been both giving and receiving food, water, shelter, electricity and healthcare independently of the aid system. They have been taking care of other people’s children, and relying on community support for transportation and the management of daily tasks like sourcing meals, finding fuel, organizing shelters and so on,” the report noted. UNRWA once again in the crosshairs On the very day that the ICJ ordered for Israel to ensure the unimpeded entry of humanitarian aid into Gaza, Washington saw fit to cut off all funding to UNRWA, the United Nations agency for Palestinian refugees. The decision came after Israel claimed that 12 UNRWA workers had been involved in the October 7 attack. UNRWA has said that it has terminated the contracts of these workers as it commissions an independent investigation into the allegations — but the United Kingdom, Australia, Italy, and Canada have followed the U.S.’s lead and pulled their funding of the organization. In an election year during which he is trying to convince the American public that he is the only alternative to the return of Donald Trump to the White House, U.S. President Joe Biden is following his predecessor’s lead, as Trump had partially suspended funding to UNRWA in 2018. “We call on the countries that announced the cessation of their support for UNRWA to immediately reverse their decision, which entails great political and humanitarian relief risks, as at this particular time and in light of the continuing aggression against the Palestinian people, we need the maximum support for this international organization and not stopping support and assistance to it,” Palestine Liberation Organization Secretary-General Hussein al-Sheikh wrote on X. Hamas, meanwhile, called on the United Nations “not to yield to the threats and blackmails.” “We stress the importance of the role of these agencies in providing relief to our people and documenting the crimes of the occupation, which exceed the most horrific crimes known to humanity in our modern era,” the movement said in a statement. Even as the U.S. appears steadfast in siding with Israel, Biden is facing legal trouble at home over his administration’s failure to stop the ongoing genocide in Gaza. Palestinians testified on Friday in front of a federal court, in a case brought forth by the Center for Constitutional Rights (CCR) against Biden, Secretary of State Antony Blinken, and Defense Secretary Lloyd Austin, arguing that the three high-ranking officials are liable under U.S. law for complicity in Israel’s violations of the Genocide Convention. Israeli forces kill Palestinian in the West Bank, exchanges of fire continue on all fronts In the occupied West Bank, Israeli forces killed at least one Palestinian overnight. Qassam Ahmad Yasin, 27, was shot and killed in the village of Deir Abu Deif near Jenin, where overnight clashes were reported between Israeli forces and Palestinian residents. Armed confrontations were also reported in Qalqilya, near the illegal Israeli settlement of Etzion, and an Israeli checkpoint in Beit Furik. Israeli forces have been setting up more flying checkpoints across the Jenin governorate in recent days, assaulting Palestinians and tearing down flags. Israeli forces detained at least eight Palestinians overnight across the West Bank, WAFA reported. Meanwhile, Friday marked the sixteenth consecutive week of Israeli restrictions for worshippers seeking to pray at the Al-Aqsa Mosque in occupied East Jerusalem. Israeli forces fired tear gas and skunk water at Palestinians seeking to enter the holy site on the Muslim day of worship. Further north, the Hezbollah movement said an Israeli airstrike on the southern Lebanese village of Beit Lif on Friday night had killed four of its members, as the Lebanese resistance movement continues to exchange fire with Israel across the Blue Line. Yemen’s Houthi rebels meanwhile struck a British-linked tanker in the Gulf of Aden on Friday. U.S. forces launched an airstrike on Hodeidah on Saturday in retaliation. BEFORE YOU GO – At Mondoweiss, we understand the power of telling Palestinian stories. For 17 years, we have pushed back when the mainstream media published lies or echoed politicians’ hateful rhetoric. Now, Palestinian voices are more important than ever. Our traffic has increased ten times since October 7, and we need your help to cover our increased expenses. Support our journalists with a donation today. https://mondoweiss.net/2024/01/operation-al-aqsa-flood-day-113-a-day-after-icj-ruling-u-s-and-allies-withdraw-funding-to-unrwa/
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    ‘Operation Al-Aqsa Flood’ Day 113: A day after ICJ ruling, U.S. and allies withdraw funding to UNRWA
    At least five countries have pulled their funding from the U.N. agency for Palestinian refugees over Israeli claims that staff members participated in the October 7 attack. Israel keeps killing Palestinians in Gaza and the West Bank.
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  • EXCLUSIVEInside NIH virus lab in Montana - that has eerie ties to Wuhan - where US scientists inject pigs and monkeys with EBOLA and other dangerous bio-agents
    By Alexa Lardieri U.S. Deputy Health Editor Dailymail.Com 14:57 GMT 27 Jan 2024 , updated 14:57 GMT 27 Jan 2024

    Photos obtained by a watchdog group show experiments performed on animals
    NIH lab in Montana was previously found to have been experimenting with SARS
    REVEALED: NIH lab experimented with coronaviruses from Wuhan in 2018
    Photos and videos obtained exclusively by DailyMail.com show US government-funded researchers experimenting on animals at a controversial lab in Montana where risky virus research is carried out.

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    Images and video footage obtained through a Freedom of Information Act request and shared exclusively with this website show researchers sedating monkeys and pigs and giving them injections, as well as piglets housed in small and unsanitary cages.

    Top Stories by Daily Mail 01:00 Admiral Rob Bauer: 'The next 20 years will not be hunky dory' MailOnline explains the top myths and facts surrounding Diabetes Prince William visits Kate as she spends her third day in hospital Crack appears in block of flats where 88 homes are being bulldozed Kate in hospital after undergoing abdominal surgery PETER HITCHENS: We don't wantdeath or blackouts, end the march to war
    While there is no suggestion any of the footage shows illegal activity, it gives an eerie glimpse into what goes on at the National Institutes of Health's Rocky Mountain Lab (RML), which has come under scrutiny in recent months.

    Last year, this website revealed that RML in Montana had been experimenting with SARS-like viruses a year before the Covid pandemic, and while that research has stopped, current projects involving other deadly pathogens with the potential to spark a new pandemic are still being carried out at the lab.

    These include injecting pigs with Ebola and infecting monkeys with Covid-19 and studying how they react to Hemorrhagic Fever, which involves vomiting blood, internal bleeding, bleeding in the brain and from the eyes, nose and mouth.

    The documents reveal NIH scientists proposed infecting two- to three-week old piglets with reston virus (REBOV), a family of pathogens that could cause Ebola, for a project to take place between 2017 and 2020
    The documents reveal NIH scientists proposed infecting two- to three-week old piglets with reston virus (REBOV), a family of pathogens that could cause Ebola, for a project to take place between 2017 and 2020
    The White Coat Waste project obtained photos of animal experiments on monkeys and pigs at the National Institutes of Health's Rocky Mountain Lab in Montana
    The White Coat Waste project obtained photos of animal experiments on monkeys and pigs at the National Institutes of Health's Rocky Mountain Lab in Montana
    The National Institutes of Health's Rocky Mountain Lab in Montana was previously found to have been experimenting with SARS-like viruses in 2018
    The National Institutes of Health's Rocky Mountain Lab in Montana was previously found to have been experimenting with SARS-like viruses in 2018
    Piglet experiments were to be carried in two parts, first infecting the pigs with REBOV via their noses - as seen in the photos above
    Piglet experiments were to be carried in two parts, first infecting the pigs with REBOV via their noses - as seen in the photos above
    The footage was obtained through a FOIA request by the White Coat Waste Project (WCW), which has campaigned against risky virus research and cruel animal experiments.

    The RML was first revealed to be experimenting with deadly pathogens in WCW's first batch of documents provided to this website last year.

    Previous documents from WCW revealed that in 2018, NIH researchers infected bats at the Rocky Mountain Lab with a 'SARS-like' virus as part of a collaboration with the Wuhan Institute of Virology, which is at the center of the Covid cover-up scandal.

    They showed US taxpayer money was used to experiment with coronaviruses from the Chinese lab thought to be the source of the Covid pandemic more than a year before the global outbreak.

    The NIH, under Dr Anthony Fauci's leadership, infected 12 Egyptian fruit bats with a 'SARS-like' virus called WIV1 at RML.

    The WIV1-coronavirus was shipped from the Wuhan lab the FBI believes caused the Covid pandemic and was tested on bats acquired from a 'roadside' Maryland zoo.

    Senators probe Fauci-run virus lab in Montana where US scientists were infecting bats with Covid-like viruses shipped in from WUHAN in 2018 - years before the pandemic


    Senators are demanding answers about a laboratory in Montana where US taxpayer money was used to manipulate coronaviruses before the pandemic.

    The research determined the novel virus could not cause a 'robust infection,' but is more evidence of ties between the US government and the Wuhan lab, as well as the funding of dangerous virus research across the globe.

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    Following the WCW's investigation and DailyMail.com's reporting, Republican Senators Joni Ernst, from Iowa, and Eric Schmitt, from Missouri, sent a letter to the NIH demanding 'to learn more about potentially risky research' carried out by scientists at RML.

    Most recently, Sen Ernst wrote another letter, along with Rep Mike Gallagher, to the Pentagon demanding a review of the $50million in grants the US is sending to Chinese pandemic research institutions, including those based in Wuhan.

    The senator said in a statement: 'Taxpayers deserve to know how much of their money is being shipped to China and why Washington continues collecting and creating deadly super viruses — both of which could pose threats to our national security.'

    While the 'SARS-like' virus research has stopped, current projects involving other deadly pathogens with the potential to spark a new pandemic are still being carried out at the lab.

    As part of WCW's current lawsuit, the NIH was compelled to send the group records of its experiments taking place at RML.

    The documents reveal NIH scientists proposed infecting two- to three-week old piglets with reston virus (REBOV), a family of pathogens that could cause Ebola, a virus with a death rate of up to 90 percent, for a project to take place between 2017 and 2020.

    The project, 'The role of Arterivirus co-infection in the pathogenesis of Reston Ebola Virus in swine', was to test how the co-infection of Porcine Reproductive and Respiratory Syndrome (PRRS) and REBOV increased the virus' transmissibility and severity.

    The experiment was to be carried out in two parts, first infecting the pigs with REBOV via their noses - as seen in photos.

    On day three and between days five and 10 after inoculation, four animals were to be euthanized so necropsies could be performed.

    The remaining animals were to be euthanized on day 28. Then, researchers proposed inoculating pigs with PRRSV and REBOV several days later to observe their behavior and take vitals then euthanize them on day 28.

    One study was to evaluate up to three species of nonhuman primates as potential animal models for Covid-19. For each species, one group of eight animals would be inoculated with a high dose of the virus via the eyes, nose or mouth
    One study was to evaluate up to three species of nonhuman primates as potential animal models for Covid-19. For each species, one group of eight animals would be inoculated with a high dose of the virus via the eyes, nose or mouth
    In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19
    In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19
    In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19
    In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19
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    While experimental 'manipulations' were to take place while the pigs were under anesthesia, the researchers said, 'Since we are evaluating these animals as potential models of disease progression, we are unable to alleviate the signs of disease.'

    Symptoms of these diseases include fever, breathing problems, weight loss, diarrhea, excessive or internal bleeding, coughing up or vomiting blood and neurological disorders that could be fatal.

    Researchers said: 'The illness experienced by animals exposed to these viruses must not be treated with analgesics because treatment will interfere with studying the disease manifestation and ultimate outcomes of infection.'

    In additional documents obtained by WCW, scientists proposed experiments between 2019 and 2022 on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever, a tick-borne virus that causes a life-threatening fever, muscle and joint pain, liver and kidney failure or pulmonary failure.

    The proposal said: 'In previous studies animals were scored for... reduced movement in cage and edema that on rare instances was of severity sufficient to impair function of internal organs such as the lungs and intestines.

    'Since the objective of this study is to evaluate the efficacy of DNA vaccine candidates against CCHFV and contains necessary irrelevant DNA control group it is expected that some or animals will develop clinical signs and may suffer pain and distress.

    'The illness experienced by the animals exposed to CCHFV must not be treated with analgesics because treatment could interfere with the disease manifestation and the outcome of vaccination.'

    Photos show piglets housed in small and unsanitary cages
    Photos show piglets housed in small and unsanitary cages
    Photos show piglets housed in small and unsanitary cages
    Photos show piglets housed in small and unsanitary cages
    A third proposal for experiments between 2020 and 2023 was titled 'Nonhuman primate model development for the novel coronavirus emerging in Wuhan, China.'

    The aim was to evaluate up to three species of nonhuman primates as potential animal models for Covid-19. For each species, one group of eight animals would be inoculated with a high dose of the virus via the eyes, nose or mouth - as seen in photos.

    The primates were to be evaluated and have their vitals taken and on day three, four would be euthanized. The remaining were to be monitored for disease progression.

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    The proposal read: 'Infection with 2019-nCoV may cause mild to severe disease in nonhuman primates. Signs of illness may include fever, malaise, fatigue cough and heavy breathing potentially resulting in acute respiratory distress; the infection may be fatal.

    'However, in this study we are unable to alleviate the disease manifestations potentially associated with 2019-nCoV infection as treatment would interfere with the outcome of the study.'

    Justin Goodman, the senior vice president of the White Coat Waste Project told DailyMail.com: 'Our successful lawsuit has pierced the veil of secrecy around the NIH’s dangerous, wasteful, and cruel maximum pain animal experiments with deadly bioagents that have up to 100 percent kill rates in humans.

    'We’ve uncovered how NIH gain-of-function researchers linked to EcoHealth and the Wuhan lab import primates to the Rocky Mountain Lab from Fauci’s Monkey Island in South Carolina, infect them with viruses including Ebola and COVID, and then completely withhold pain relief while the animals suffer excruciating deaths.

    'Taxpayers have a right to know how their money is being spent in barbaric NIH animal labs that can cause a devastating lab leak and pandemic right here in the US.'

    https://www.dailymail.co.uk/health/article-13008119/montana-lab-scientists-experimenting-dangerous-pathogens.html
    EXCLUSIVEInside NIH virus lab in Montana - that has eerie ties to Wuhan - where US scientists inject pigs and monkeys with EBOLA and other dangerous bio-agents By Alexa Lardieri U.S. Deputy Health Editor Dailymail.Com 14:57 GMT 27 Jan 2024 , updated 14:57 GMT 27 Jan 2024 Photos obtained by a watchdog group show experiments performed on animals NIH lab in Montana was previously found to have been experimenting with SARS REVEALED: NIH lab experimented with coronaviruses from Wuhan in 2018 Photos and videos obtained exclusively by DailyMail.com show US government-funded researchers experimenting on animals at a controversial lab in Montana where risky virus research is carried out. Advertisement Advertisement Images and video footage obtained through a Freedom of Information Act request and shared exclusively with this website show researchers sedating monkeys and pigs and giving them injections, as well as piglets housed in small and unsanitary cages. Top Stories by Daily Mail 01:00 Admiral Rob Bauer: 'The next 20 years will not be hunky dory' MailOnline explains the top myths and facts surrounding Diabetes Prince William visits Kate as she spends her third day in hospital Crack appears in block of flats where 88 homes are being bulldozed Kate in hospital after undergoing abdominal surgery PETER HITCHENS: We don't wantdeath or blackouts, end the march to war While there is no suggestion any of the footage shows illegal activity, it gives an eerie glimpse into what goes on at the National Institutes of Health's Rocky Mountain Lab (RML), which has come under scrutiny in recent months. Last year, this website revealed that RML in Montana had been experimenting with SARS-like viruses a year before the Covid pandemic, and while that research has stopped, current projects involving other deadly pathogens with the potential to spark a new pandemic are still being carried out at the lab. These include injecting pigs with Ebola and infecting monkeys with Covid-19 and studying how they react to Hemorrhagic Fever, which involves vomiting blood, internal bleeding, bleeding in the brain and from the eyes, nose and mouth. The documents reveal NIH scientists proposed infecting two- to three-week old piglets with reston virus (REBOV), a family of pathogens that could cause Ebola, for a project to take place between 2017 and 2020 The documents reveal NIH scientists proposed infecting two- to three-week old piglets with reston virus (REBOV), a family of pathogens that could cause Ebola, for a project to take place between 2017 and 2020 The White Coat Waste project obtained photos of animal experiments on monkeys and pigs at the National Institutes of Health's Rocky Mountain Lab in Montana The White Coat Waste project obtained photos of animal experiments on monkeys and pigs at the National Institutes of Health's Rocky Mountain Lab in Montana The National Institutes of Health's Rocky Mountain Lab in Montana was previously found to have been experimenting with SARS-like viruses in 2018 The National Institutes of Health's Rocky Mountain Lab in Montana was previously found to have been experimenting with SARS-like viruses in 2018 Piglet experiments were to be carried in two parts, first infecting the pigs with REBOV via their noses - as seen in the photos above Piglet experiments were to be carried in two parts, first infecting the pigs with REBOV via their noses - as seen in the photos above The footage was obtained through a FOIA request by the White Coat Waste Project (WCW), which has campaigned against risky virus research and cruel animal experiments. The RML was first revealed to be experimenting with deadly pathogens in WCW's first batch of documents provided to this website last year. Previous documents from WCW revealed that in 2018, NIH researchers infected bats at the Rocky Mountain Lab with a 'SARS-like' virus as part of a collaboration with the Wuhan Institute of Virology, which is at the center of the Covid cover-up scandal. They showed US taxpayer money was used to experiment with coronaviruses from the Chinese lab thought to be the source of the Covid pandemic more than a year before the global outbreak. The NIH, under Dr Anthony Fauci's leadership, infected 12 Egyptian fruit bats with a 'SARS-like' virus called WIV1 at RML. The WIV1-coronavirus was shipped from the Wuhan lab the FBI believes caused the Covid pandemic and was tested on bats acquired from a 'roadside' Maryland zoo. Senators probe Fauci-run virus lab in Montana where US scientists were infecting bats with Covid-like viruses shipped in from WUHAN in 2018 - years before the pandemic Senators are demanding answers about a laboratory in Montana where US taxpayer money was used to manipulate coronaviruses before the pandemic. The research determined the novel virus could not cause a 'robust infection,' but is more evidence of ties between the US government and the Wuhan lab, as well as the funding of dangerous virus research across the globe. Advertisement Advertisement Following the WCW's investigation and DailyMail.com's reporting, Republican Senators Joni Ernst, from Iowa, and Eric Schmitt, from Missouri, sent a letter to the NIH demanding 'to learn more about potentially risky research' carried out by scientists at RML. Most recently, Sen Ernst wrote another letter, along with Rep Mike Gallagher, to the Pentagon demanding a review of the $50million in grants the US is sending to Chinese pandemic research institutions, including those based in Wuhan. The senator said in a statement: 'Taxpayers deserve to know how much of their money is being shipped to China and why Washington continues collecting and creating deadly super viruses — both of which could pose threats to our national security.' While the 'SARS-like' virus research has stopped, current projects involving other deadly pathogens with the potential to spark a new pandemic are still being carried out at the lab. As part of WCW's current lawsuit, the NIH was compelled to send the group records of its experiments taking place at RML. The documents reveal NIH scientists proposed infecting two- to three-week old piglets with reston virus (REBOV), a family of pathogens that could cause Ebola, a virus with a death rate of up to 90 percent, for a project to take place between 2017 and 2020. The project, 'The role of Arterivirus co-infection in the pathogenesis of Reston Ebola Virus in swine', was to test how the co-infection of Porcine Reproductive and Respiratory Syndrome (PRRS) and REBOV increased the virus' transmissibility and severity. The experiment was to be carried out in two parts, first infecting the pigs with REBOV via their noses - as seen in photos. On day three and between days five and 10 after inoculation, four animals were to be euthanized so necropsies could be performed. The remaining animals were to be euthanized on day 28. Then, researchers proposed inoculating pigs with PRRSV and REBOV several days later to observe their behavior and take vitals then euthanize them on day 28. One study was to evaluate up to three species of nonhuman primates as potential animal models for Covid-19. For each species, one group of eight animals would be inoculated with a high dose of the virus via the eyes, nose or mouth One study was to evaluate up to three species of nonhuman primates as potential animal models for Covid-19. For each species, one group of eight animals would be inoculated with a high dose of the virus via the eyes, nose or mouth In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19 In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19 In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19 In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19 Advertisement Advertisement While experimental 'manipulations' were to take place while the pigs were under anesthesia, the researchers said, 'Since we are evaluating these animals as potential models of disease progression, we are unable to alleviate the signs of disease.' Symptoms of these diseases include fever, breathing problems, weight loss, diarrhea, excessive or internal bleeding, coughing up or vomiting blood and neurological disorders that could be fatal. Researchers said: 'The illness experienced by animals exposed to these viruses must not be treated with analgesics because treatment will interfere with studying the disease manifestation and ultimate outcomes of infection.' In additional documents obtained by WCW, scientists proposed experiments between 2019 and 2022 on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever, a tick-borne virus that causes a life-threatening fever, muscle and joint pain, liver and kidney failure or pulmonary failure. The proposal said: 'In previous studies animals were scored for... reduced movement in cage and edema that on rare instances was of severity sufficient to impair function of internal organs such as the lungs and intestines. 'Since the objective of this study is to evaluate the efficacy of DNA vaccine candidates against CCHFV and contains necessary irrelevant DNA control group it is expected that some or animals will develop clinical signs and may suffer pain and distress. 'The illness experienced by the animals exposed to CCHFV must not be treated with analgesics because treatment could interfere with the disease manifestation and the outcome of vaccination.' Photos show piglets housed in small and unsanitary cages Photos show piglets housed in small and unsanitary cages Photos show piglets housed in small and unsanitary cages Photos show piglets housed in small and unsanitary cages A third proposal for experiments between 2020 and 2023 was titled 'Nonhuman primate model development for the novel coronavirus emerging in Wuhan, China.' The aim was to evaluate up to three species of nonhuman primates as potential animal models for Covid-19. For each species, one group of eight animals would be inoculated with a high dose of the virus via the eyes, nose or mouth - as seen in photos. The primates were to be evaluated and have their vitals taken and on day three, four would be euthanized. The remaining were to be monitored for disease progression. Advertisement Advertisement The proposal read: 'Infection with 2019-nCoV may cause mild to severe disease in nonhuman primates. Signs of illness may include fever, malaise, fatigue cough and heavy breathing potentially resulting in acute respiratory distress; the infection may be fatal. 'However, in this study we are unable to alleviate the disease manifestations potentially associated with 2019-nCoV infection as treatment would interfere with the outcome of the study.' Justin Goodman, the senior vice president of the White Coat Waste Project told DailyMail.com: 'Our successful lawsuit has pierced the veil of secrecy around the NIH’s dangerous, wasteful, and cruel maximum pain animal experiments with deadly bioagents that have up to 100 percent kill rates in humans. 'We’ve uncovered how NIH gain-of-function researchers linked to EcoHealth and the Wuhan lab import primates to the Rocky Mountain Lab from Fauci’s Monkey Island in South Carolina, infect them with viruses including Ebola and COVID, and then completely withhold pain relief while the animals suffer excruciating deaths. 'Taxpayers have a right to know how their money is being spent in barbaric NIH animal labs that can cause a devastating lab leak and pandemic right here in the US.' https://www.dailymail.co.uk/health/article-13008119/montana-lab-scientists-experimenting-dangerous-pathogens.html
    WWW.DAILYMAIL.CO.UK
    Inside NIH lab where US scientists experiment with dangerous pathogens
    Photos and videos obtained exclusively by DailyMail.com show US researchers experimenting on animals (pictured) at a controversial lab in Montana where risky virus research is carried out.
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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
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    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/


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    https://www.vtforeignpolicy.com/2024/01/terrifying-new-lethal-bio-weapon-sars-cov-3-built-and-hid-by-chinas-army/
    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/
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    Terrifying! New LETHAL BIO-WEAPON SARS-COV-3 Built and Hid by CHINA’s ARMY
    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...
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