A Question of Parental RIghts

 

NEWS

Radicals Threaten to Kill, Dismember School Board President for Adopting Parental Rights Policy

July 25, 2023

A local school board president has been inundated with threats that left-wing activists will dismember her, murder her children, and slaughter her pets. Her crime? Saying that teachers should not keep parents in the dark if their children begin to identify as transgender.

The new Chino Valley (California) Unified School District Board of Education policy states that school officials will notify parents in writing within three days if a child seeks to identify as a gender “other than the student’s biological sex,” use different pronouns, adopt a different name, use the restroom, or join a sports team of the opposite sex. The board adopted the resolution last Thursday, July 20, by a 4-1 vote, with member Donald Bridge casting the lone dissenting vote.

“The next morning, our district got a phone call” from an anonymous caller threatening “to kill me, and they said that they were going to dismember” school board president Sonja Shaw, the official revealed on “Washington Watch with Tony Perkins” Monday. Police alerted Shaw to the threat shortly before a previous interview on the show, last Friday.

Then Shaw looked at her district email account, where she said she saw messages stating, “You’re going to die,” with a series of profane epithets. “Your children are going to die and your animals are going to die.” For a “point of reference, they would name what kind of animals I had,” Shaw added.

“I also got notification that people who identify as being in the terrorist organization Antifa posted on their website, ‘We declare war on Sonja Shaw,’” Shaw told Perkins, adding that the group posted her address. “They said, ‘We know where you sleep,’” the same message an angry mob screamed outside the home of Tucker Carlson in 2018. “They said things like, ‘Use all force possible to stop her.’”

“I’m not going to lie. I was shaking,” Shaw confided on Monday. Police had beefed up patrols around her home to ensure security, she said.

While she had been “hesitant” to share the details of her ordeal, “God reminded me that these are the people that are after our children.”

“Sacramento has waged a war on parental rights, and a lot of it has to do with the perversion of our children,” Shaw told “Washington Watch” guest host Jody Hice, a former Georgia congressman, on Friday.

“We have to put up safeguards. That’s why I was put here,” Shaw told the school board meeting on Thursday.

After being alarmed by Democratic Governor Gavin Newsom’s top-down imposition of radical education policy as a parent, Shaw ran for school board, and “God opened the doors” to implement the new policy, she told Hice. When the Newsom administration learned of the impending policy, State Superintendent Tony Thurmond arrived at the district meeting Thursday night.

“It was a political stunt. He was trying to scare us,” assessed Shaw.

Thurmond requested a private meeting with Shaw prior to the meeting but declined to follow through when he learned she would not withdraw the policy, Shaw has said. He instead addressed the board meeting, speaking as the first of 83 citizens to make their voices heard. Video footage shows the attendees booed when Thurmond concluded, as Shaw asked everyone to “be respectful” toward the official. Thurmond exceeded his one-minute speaking slot, then returned to the podium demanding a “point of order,” although he is not a board member. Police eventually escorted him out of the building.

Thurmond later claimed he “stayed within the one-minute limit,” and tweeted, “When done speaking, the board president verbally attacked me an [sic] instructed police to remove me.” State Senator Scott Wiener (D-San Francisco), who authored a bill allowing out-of-state children who identify as transgender to flee to California and be injected with cross-sex hormones against their parents’ wishes, alleged, “The QAnon school board president cut him off.” But his former colleague, State Senator Melissa Melendez (R-67), pointed out that “Thurmond militantly enforced the rules for speakers when he was in the legislature.”

The district’s newly enacted policy has won the support of parental rights advocates and education experts nationwide. “The school board in Chino Valley is making parental involvement and inclusion a priority. State level officials interested in a healthy school system should follow their lead,” Meg Kilgannon, senior fellow for Education Studies at Family Research Council, told The Washington Stand.

But the policy drew instant backlash from the California Legislative LGBTQ Caucus, which announced its members are already “actively working on new approaches” to override the democratically enacted resolution. The liberal caucus added that parents who represented the near-unanimous consensus of the Chino Valley school board “will not stop us.”

“It appears some state legislators are scheming to make the newly passed CVUSD policy illegal with a future bill,” said Jonathan Zachreson, a member of the Roseville City School District school board and the founder of Reopen California Schools.

Parents in the district have expressed enthusiastic approval. “I think it’s crucial that we keep parents in this conversation. I think that the worst thing you can do to a child is to ostracize their parents from such an important conversation,” Amy Davlin, a parent in the district, told Newsmax on Tuesday morning.

“Groomers and pedophiles are the ones who attempt to gain the trust of children and encourage them to keep secrets” from their parents, said Davlin. A school district should “not encourage children to deceive and lie to their parents.”

More than two-thirds (68%) of Californians agree that parents should be notified if their minor children change their gender identity, according to a poll taken by Protect Kids California.

“I believe there is an all-out agenda against our children,” said Davlin, who said the new policy sends a message to activists who have weaponized education against parents: “You have crossed a red line. The red line is our children.”

Democrats have indicated a legal fight will ensue. California State Attorney General Rob Bonta (D) threatened that the pro-parental rights policy “may violate California’s antidiscrimination law” in a letter to the Chino Valley school board seeking to sway Thursday’s vote. Disclosing a child’s transgender identification to his or her parents “is very likely to result in significant emotional, mental, and even physical harm,” Bonta asserted.

Parents and board members reject that talking point. “Why are you assuming that parents are dangerous?” asked Shaw.

“If you want a lower suicide rate, bring the parents into the conversation,” said Davlin. “We are the ones who love the kids the most. We are the ones who have their best interests at heart, not their teacher who is with them a few hours a day.”

As Newsom and Thurmond focus on social issues, California students fall further behind. California ranks 38th nationwide in K-12 education, according to U.S. News and World Report — behind such Republican strongholds as Florida (14), Virginia (13), Indiana (7), Utah (9), Nebraska (11), and South Dakota (24). Education levels may improve if teachers focused on fundamentals rather than indoctrination, said Kilgannon. “We’re just trying to get the crazy out: To not have children taught wrong history, not have children taught that they could be born in the wrong body, not have children shown sexually explicit images,” she told Perkins on Monday.

Shaw’s leadership could show the Republicans how to recapture the White House in 2024, one political commentator believes. “We need to have more Sonjas running the school boards around the country,” said Newsmax contributor Tom Borelli on Monday morning. “Republicans can make this a great issue going forward, that we’re the party that represents parental rights. How dare a school district try to deny a parent knowledge about their own child?! That’s just plain outrageous.”

Meanwhile a potential 2024 Democratic presidential hopeful, Gavin Newsom, “plays the biggest part” in fueling the vitriol, hatred, and potential violence directed toward the Chino Valley school board, said Shaw. “But I’m glad that they’re exposing themselves,” Shaw continued.

“My daily prayer is for those to be revealed, exposed, and removed that don’t have the best intentions and that have ill intent for children,” Shaw told Perkins. Thanks to their voluble radicalism, “More people are starting to realize what we’re up against.”

“They’re literally driving a wedge between parent and child,” said Perkins on Monday. “This is evil. It’s just pure evil.”

from:    https://washingtonstand.com/news/radicals-threaten-to-kill-dismember-school-board-president-for-adopting-parental-rights-policy

 

Autopsy Reports Reveal…..

Study: 74% of Post-Jab Deaths Caused by the Shot

Analysis by Dr. Joseph MercolaFact Checked 

https://rumble.com/v2ykrv8-doctors-censored-by-lancet-in-paper-that-found-74-mrna-vaccine-related-caus.html

STORY AT-A-GLANCE

  • July 5, 2023, Dr. Peter McCullough, Dr. Harvey Risch, Dr. Roger Hodkinson, an expert clinical pathologist, and colleagues published a systematic review of autopsy findings in people who died after receiving a COVID shot on The Lancet journal’s preprint server
  • The autopsy review found that 62.5% to 73.9% of post-jab deaths were likely caused by the injection
  • Preprints with The Lancet pulled the study in less than 24 hours
  • The New England Journal of Medicine (NEJM) also rejected the paper, as did the Journal of the American Medical Association (JAMA). The preprint server medRxiv and others also refused to post it
  • Belgian researchers report that two doses of the Pfizer mRNA COVID jab induced lethal “turbo cancers” in a mouse. Two days after receiving its second dose, one of the 14 injected mice (7%) died suddenly. No clinical signs of illness were present before its abrupt death. Upon post-mortem examination, the mouse was found to have lymphoma in several organs, including the heart, liver, kidneys, spleen and lungs

July 5, 2023, Dr. Peter McCullough, Dr. Harvey Risch, Dr. Roger Hodkinson, an expert clinical pathologist, and several other colleagues published a systematic review of autopsy findings in people who died after receiving a COVID shot on The Lancet journal’s preprint server.1

Disturbingly, but not surprisingly, they concluded that 62.5% to 73.9% of post-jab deaths were likely caused by the injection. Previous autopsy reviews have also concluded that the mRNA COVID jabs are a causative factor in sudden cardiac deaths.2

Nearly Three-Quarters of Post-Jab Deaths Caused by the Shot

As explained by the authors:3

“The aim of this systematic review is to investigate possible causal links between COVID-19 vaccine administration and death using autopsies and post-mortem analysis … We searched for all published autopsy and necropsy reports relating to COVID-19 vaccination up until May 18th, 2023.

We initially identified 678 studies and, after screening for our inclusion criteria, included 44 papers that contained 325 autopsy cases and one necropsy case. Three physicians independently reviewed all deaths and determined whether COVID-19 vaccination was the direct cause or contributed significantly to death.

The most implicated organ system in COVID-19 vaccine-associated death was the cardiovascular system (53%), followed by the hematological system (17%), the respiratory system (8%), and multiple organ systems (7%). Three or more organ systems were affected in 21 cases.

The mean time from vaccination to death was 14.3 days. Most deaths occurred within a week from last vaccine administration. A total of 240 deaths (73.9%) were independently adjudicated as directly due to or significantly contributed to by COVID-19 vaccination …

Among adjudicators, there was complete independent agreement (all three physicians) of vaccination causing or contributing to death in 203 cases (62.5%). The one necropsy case was judged to be linked to vaccination with complete agreement …

The consistency seen among cases in this review with known COVID-19 vaccine adverse events, their mechanisms, and related excess death, coupled with autopsy confirmation and physician-led death adjudication, suggests there is a high likelihood of a causal link between COVID-19 vaccines and death in most cases.”

The Lancet Censors Paper

As has so often been the case over these past three years, the journal didn’t waste time censoring the paper. Preprints with The Lancet pulled it within 24 hours,4 stating “the study’s conclusions are not supported by the study methodology.”5 In what way? They don’t say. As noted by McCullough, the methodology is as standard as it gets. Will Jones at the Daily Sceptic adds:6

“A number of the authors of the paper are at the top of their fields so it is hard to imagine that the methodology of their review was really so poor that it warranted removal at initial screening rather than being subject to full critical appraisal. It smacks instead of raw censorship of a paper that failed to toe the official line …

Dr. Clare Craig, a pathologist and co-Chair of the HART pandemic advisory group, says that in her view the approach taken in the study is sound. She told the Daily Sceptic:

‘The VAERS system … is designed to alert to potential harms without necessarily being the best way of measuring the extent of those harms. Quantifying the impact of deaths can be done by looking at overall mortality rates in a country.

However, this is imperfect as a deficit of deaths would be expected after a period of excess deaths, making the accuracy of any baseline dubious. An alternative approach of auditing such deaths through autopsy is sound.

There may be a bias [in the study] towards reporting the autopsies of deaths where there was evidence of causation and the likelihood of causation might be exaggerated by that bias. For example, 19 of the 325 deaths were due to vaccine-induced immune thrombocytopenia and thrombosis (VITT) but these reports may be overrepresented because of the regulators’ willingness to acknowledge such deaths.

Nevertheless, it is important that attempts are made to quantify the risk of harm and censorship of these attempts, rather than open scientific critique, does nothing to help reassure people.”

Prior to this, The New England Journal of Medicine (NEJM) had also rejected the paper, as had the Journal of the American Medical Association (JAMA). NEJM rejected it within a few days, and JAMA within about an hour of submission. The preprint server medRxiv and others also refused to post it.

In the video above, Naomi Wolf with Daily Clout interviewed McCullough about the censoring of his paper. According to McCullough, overnight, while the paper was still on the Preprint server, downloads of the paper were in the hundreds per minute, demonstrating there’s a clear demand for this information.

The paper is currently only available for download on the preprint server Zenodo.7 Ironically, by pulling the paper off the server, The Lancet magnified its existence, as news of the censorship went viral on social media.

Mechanisms of Action

In the featured Daily Clout interview, McCullough explains the jab’s mechanisms of action that appear to be responsible for a majority of post-jab heart-related deaths. The first is myocarditis (heart inflammation). The other is progression of atherosclerotic cardiovascular disease.

In myocarditis, the electrical current can no longer conduct smoothly through the heart muscle, causing an abnormal heart rhythm. This abnormal heart rhythm can then lead to sudden cardiac death. This is one of the primary reasons behind many athletic deaths, where players have died on the field.

In a letter to the editor of the Scandinavian Journal of Immunology published in late 2022,8,9 McCullough compared the pre- and post-COVID jab cardiac death rates among athletes, finding that before the jab, there were an average of 29 cardiac-related deaths among pro athletes per year.

After the rollout of the jab, which was mandated on players, it shot up to 283 per year — a 10-fold increase. And, in many cases, players have no prior symptoms. Wolf points out that lipid nanoparticles have been found to damage electrical conduction in the myelin sheath, so why would it not also damage electrical conduction in the heart? It makes sense that it would.

McCullough adds that when lipid nanoparticles are taken up by human somatic cells — nonreproductive cells, found in the heart and other internal organs — it causes syncytia formation where cell membranes fuse together.

And, because the heart prefers lipids over glucose for fuel, it may preferentially take up lipid nanoparticles, more so than other tissues. On top of that, exercise increases blood flow, which draws more lipid nanoparticles to the heart.

He also cites research showing there are two primary periods of sudden cardiac death: during exercise and between 3 AM and 6 AM. The common factor between these two is adrenaline. Adrenaline surges during exercise and in the natural waking process. If you have myocarditis, this adrenaline surge can be enough to trigger sudden cardiac death.

Shining a Light on Possible Treatments

As noted by Wolf, by clearly identifying how the COVID jab is killing people, McCullough’s paper also helps shed light on potential treatments. The spike protein produced by your body in response to the mRNA shot is the primary culprit that needs to be degraded and eliminated.

The enzymes in your body that would normally do this job are unable to degrade the synthetic spike protein, but there are products that can get the job done. McCullough refers to Japanese research that found nattokinase can be very helpful in this regard. However, lumbrokinase is a much stronger fibrinolytic enzyme and would likely work better.

Bromelain, an enzyme derived from pineapple stems, also works, McCullough says, as does curcumin, the active ingredient in turmeric. We also know that both hydroxychloroquine and ivermectin aid in the elimination of spike protein.

As noted by McCullough, it’s interesting that while the SARS-CoV-2 virus and the spike protein produced by the mRNA jab are synthetic and wholly unnatural, most of the best remedies are turning out to be all-natural compounds.

Reprehensible Medical Censorship

At the end of the interview, McCullough says that if the current censorship trend continues, medical history may well state that the COVID shots are perfectly safe, even though there’s plenty of evidence to the contrary — evidence that was never allowed to be seen.

In a three-part series for TrialSite News, published in 2021, investigative journalist Sonia Elijah reviewed how scientific journals were censoring the science on COVID. July 7, 2023, she published a follow-up based on the most recent censoring of McCullough’s paper:10

“This is just another example of a paper with findings, not fitting in with the ‘very good safety profile of the COVID-19 vaccines,’ being expelled from a prominent journal,” she writes. “Dr. McCullough commented exclusively for TrialSite about this highly concerning issue. This is what he said:

‘This act of medical censorship occurred after the paper met all the criteria for listing on the Lancet PrePrint Server and appears to be triggered by very heavy worldwide interest and rapid downloading of the paper.

This speaks to the importance of our findings as the largest summary of autopsies after COVID-19 vaccination. Elsevier and Lancet are trying to suppress critical scientific observations on COVID-19 vaccine safety. Their actions are reprehensible.’

My own research11 in analyzing the Periodic Safety Update Reports compiled by Pfizer for the European Medicines Agency revealed damning data. As of June 2022, 161 children have died shortly after taking the Pfizer-BioNTech COVID-19 vaccine.

What is even more shocking is that an overwhelming majority of autopsies were not performed or followed up by the pharmaceutical behemoth … This is why McCullough et al.’s study is so key because there is an incredible lack of laboratory data and post-mortem information on these post-vaccine deaths …

This begs the all-important question — has this scarcity been carefully orchestrated to prevent sufficient evidence of a causal association of COVID-19 vaccines with the reported deaths?”

Case Report of mRNA Jab-Induced Turbo Cancers

In related news, Belgian researchers report that two doses of the Pfizer mRNA COVID jab induced lethal “turbo cancers” in a mouse. Two days after receiving its second dose, one of the 14 injected mice (7%) died suddenly. No clinical signs of illness were present before its abrupt death.

Upon post-mortem examination, the mouse was found to have lymphoma in several organs, including the heart, liver, kidneys, spleen and lungs. The case report, published in Frontiers in Oncology May 1, 2023, noted:12

“Two days following booster vaccination (i.e., 16 days after prime), at only 14 weeks of age, our animal suffered spontaneous death with marked organomegaly and diffuse malignant infiltration of multiple extranodal organs (heart, lung, liver, kidney, spleen) by lymphoid neoplasm.

Immunohistochemical examination revealed organ sections positive for CD19, terminal deoxynucleotidyl transferase, and c-MYC, compatible with a B-cell lymphoblastic lymphoma immunophenotyped …

Given the paucity of data on the long-term safety of the SARS-CoV-2 mRNA vaccines, it is vital that clinicians and scientists report any adverse event to establish potential correlations.

Our case adds to previous clinical reports on malignant lymphoma development following novel SARS-CoV-2 mRNA vaccination. Interestingly, we are the first to report a B-LBL subtype …

Although strong evidence proving or refuting a causal relationship between SARS-CoV-2 mRNA vaccination and lymphoma development or progression is lacking, vigilance is required, with conscientious reporting of similar cases and a further investigation of the mechanisms of action that could explain the aforementioned association.”

Resources for Those Injured by the COVID Jab

Aside from autopsy assessments, case reports of harms and various other studies, things like job statistics, disability claims, life insurance claims and all-cause mortality statistics also tell us that the COVID jabs are having a devastating effect.13 All have skyrocketed since the introduction of these COVID jabs.

If you got one or more jabs and suffered an injury, first and foremost, never ever take another COVID booster, another mRNA gene therapy shot or regular vaccine. You need to end the assault on your body.

The same goes for anyone who has taken one or more COVID jabs and had the good fortune of not experiencing debilitating side effects. Your health may still be impacted long-term, so don’t take any more shots.

When it comes to treatment, it seems like many of the treatments that worked against severe COVID-19 infection also help ameliorate adverse effects from the jab. This makes sense, as the toxic, most damaging part of the virus is the spike protein, and that’s what your whole body is producing if you got the jab.

As mentioned earlier, eliminating the spike protein is a primary task to prevent and/or address post-jab injuries. Ivermectin and hydroxychloroquine bind to and facilitate the removal of spike protein. According to McCullough, nattokinase, bromelain and curcumin also help degrade the spike protein.

For a comprehensive treatment plan, see the Front Line COVID-19 Critical Care Alliance (FLCCC) I-RECOVER protocol. It’s continuously updated as more data become available, so be sure to download the latest version straight from the FLCCC website at covid19criticalcare.com.14

from:    https://articles.mercola.com/sites/articles/archive/2023/07/18/post-covid-vaccination-deaths.aspx?ui=f460707c057231d228aac22d51b97f2a8dcffa7b857ec065e5a5bfbcfab498ac&sd=20211017&cid_source=dnl&cid_medium=email&cid_content=art1HL&cid=20230718_HL2&foDate=true&mid=DM1435273&rid=1858959125

Thirsty in the Woods?

Survival Skills: 10 Ways to Purify Water

Access to safe drinking water is critical in camping or survival situations

One of the top survival priorities in an emergency is to find and disinfect enough drinking water to supply your needs. Whether your crisis situation is unfolding in the desert after becoming lost or in your own home after a natural disaster, the human body can only last three days without any drinking water at all. Good thing there are abundant water sources across most of the globe, and multiple ways to disinfect the water. Which method of water processing is right for different situations? Follow along here and find out.
One of the top survival priorities in an emergency is to find and disinfect enough drinking water to supply your needs. Whether your crisis situation is unfolding in the desert after becoming lost or in your own home after a natural disaster, the human body can only last three days without any drinking water at all. Good thing there are abundant water sources across most of the globe, and multiple ways to disinfect the water. Which method of water processing is right for different situations? Follow along here and find out.
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One of the top survival priorities in an emergency is to find and disinfect enough drinking water to supply your needs. Whether your crisis situation is unfolding in the desert after becoming lost or in your own home after a natural disaster, the human body can only last three days without any drinking water at all.

Good thing there are abundant water sources across most of the globe, and multiple ways to disinfect the water. Which method of water processing is right for different situations? Follow along here and find out.

tree sap spigot

Finding a Water Source

Depending on your location and situation, water can be abundant or virtually non-existent.

Before you can disinfect the water, you have to find it. Depending on your location and situation, water can be abundant or virtually non-existent. Water can come from freshwater surface sources like streams, creeks, ponds, and lakes. If you are able to distill the water, you can even use brackish or salty water as a source.

Let’s not forget precipitation as an emergency water supply. Rain, snow, sleet, hail, ice, and dew can be collected for water. Fresh rain that didn’t fall through a jungle or forest canopy should be safe enough to drink as is. New snow can be melted for drinking without processing as well.

Water issuing from springs and other underground sources can also be safe in most areas. Water coming from tapped trees like maple and birch can be safe to drink and abundant in late winter. But most other water sources should be considered “dirty” and must be disinfected with one of the following methods.

boiling water

Boiling

In order to kill the parasites, bacteria, and other pathogens in water, the most reliable thing to do is boil the water.

In order to kill the parasites, bacteria, and other pathogens in water, the most reliable thing to do is boil the water. Boiling will not evaporate all forms of chemical pollution, but it is still one of the safest methods of disinfection. Five minutes of a rolling boil will kill most organisms, but ten minutes is safer. Elevations high enough to effect boiling and cooking times will require slightly more time over the flame.

Boiling can be done over a campfire or stove in a metal, ceramic, or glass container. If no fireproof container is available, heat rocks for 30 minutes in the fire and place them into your container of water. This container could be a rock depression, a bowl burned out of wood, a folded bark container, a hide, or an animal stomach. Don’t use quartz or any river rocks as these can explode when heated.

distillation still

Distillation

In a scenario where the only water available is dangerous water, there aren’t many options. The safest solution is water distillation.

Radiation, lead, salt, heavy metals, and many other contaminants can taint your water supply after a disaster, and trying to filter them out will only ruin your expensive water filter.

In a scenario where the only water available is dangerous water, there aren’t many options. The safest solution is water distillation. Water can be heated into steam, and the steam can then be captured to create relatively clean water, despite its prior forms of contamination—including radioactive fallout. Distillation won’t remove all possible contaminants, like volatile oils and certain organic compounds, but most heavy particles will stay behind. For home-based disaster survival situations, a quick way to make a steam distiller is with a pressure canner and some small-diameter copper tubing. The best part of this operation (aside from safe water) is that the canner stays intact. This allows you to shift gears from water distillation to food preservation very easily (providing you are not dealing with radiation). The only tricky part is getting the copper line fitted to the steam vent on the canner’s lid.

If in the field, try your luck with a solar still, a simple invention that collects and distills water in a hole in the ground. To build one, place a square of clear or milky plastic (5×5 or 6×6 feet) over a three-feet-deep hole with a clean container centered in the bottom. (Run a drinking tube from the container so that you can drink your gathered water without taking apart the whole still.) Place dirt around the edge of the plastic at the rim of the hole to seal off the still. Place a rock in the middle of the plastic to create a roughly 45-degree cone over the container. Dig the still in a sunny location and in the dampest dirt or sand available. Add green vegetation and even urine to the hole to increase its water production. A transpiration bag is a smaller and less productive version of this set-up, involving a clear plastic bag tied around live vegetation.

Lifestraw

Survival Straws

One of the smallest, lightest of water disinfecting tools to hit the marketplace lately is the straw style of water filter.

One of the smallest, lightest of water disinfecting tools to hit the marketplace lately is the straw style of water filter. Newer models can be used as you would a drinking straw and can also connect to the drain valve on a water heater to clean up the water you might find in a water heater after a disaster. They can also fit onto a garden hose to filter the water running through it. Don’t expect it to filter out every single virus or bacteria that could be growing in there, though—especially a hose that’s been laying in the sun, or a water heater full of tepid water after a prolonged power outage. Most of these filters contain an activated carbon filter element, which not only filters out larger bacteria and pathogens, but also removes odd flavors and odors from the water.

water filter IV bag

Filters

The two main types of water filters in use today are pump-action filters and drip/suction filters.

The two main types of water filters in use today are pump-action filters and drip/suction filters. The former utilize a pump to force raw water through a filter cartridge. The latter are filter cartridges that use a gravity drip action (like an IV bag) or are placed in line on hydration bladder hoses. When used on a hydration bladder, the user simply sucks water through the filter as needed. My favorite (for years now) is the Katadyn Pocket filter. It has a ceramic cartridge with silver imbedded inside. The ceramic filters out the larger pathogens, and the silver kills or disables smaller organisms like viruses. Most filters like this will pump about a quart per minute. If time isn’t an issue, you might opt for a gravity-fed system like the one shown here.

UV light filter

UV Light Devices

UV light is very damaging to small organisms. When used as a disinfection method, it’s surprisingly effective.

UV light is very damaging to small organisms. When used as a disinfection method, it’s surprisingly effective. Devices like the Steripen Sidewinder are battery-free, hand-cranked water purification devices that disrupt the DNA of illness-causing microbes in mere seconds. There are also a few battery-powered Steripen products that pack the same punch on bad bugs, and have been field-proven around the globe. These are not 100-percent effective in water with large floating particles (which pathogens can hide behind or inside), but for clear water of questionable origin these devices will do the trick.

solar water disinfection

SODIS

Solar water disinfection (SODIS for short) is a water treatment method that uses the sun’s energy for disinfection.

Solar water disinfection (SODIS for short) is a water treatment method that uses the sun’s energy for disinfection. The most common technique is to expose plastic bottles full of contaminated water to the sun for a minimum of one day. The sun’s abundant UV light kills or damages almost all biological hazards in the water. The advantages to this way of treating water are plentiful. It’s easy to use; it’s inexpensive or free; and it offers good (but not complete or guaranteed) bacterial and viral disinfection. Furthermore, the method uses no dangerous chemicals, and it does not require constant attention.

But there are some problems with the method. You need sunny weather or two days of overcast sky to reach the maximum effectiveness. You cannot use it in rain; it offers no residual disinfection; it may be less effective against bacterial spores and cyst stages of some parasites; the water and the bottle need to be clear; and the bottle shouldn’t be glass. If that wasn’t bad enough, this method does nothing to help with chemical contamination, and only small bottles (2 liters, max) can be processed.

water disinfection tablets

Disinfecting Tablets

While these two products are using different chemicals, they both seem to be better than 99-percent effective against water-borne pathogens.

Two of the most common and popular water disinfection tablets are Katadyn’s Micropur tablets and Potable Aqua’s iodine tablets. They can both work very effectively, but there are some differences. If you’re stocking a cabin, cave, or BOB with purification tablets, you certainly want to consider the life span of the product. The iodine tablets from Potable Aqua have a one-year shelf life. That’s not bad, but Katadyn‘s Micropur tablets last for two years or more. While these two products are using different chemicals, they both seem to be better than 99-percent effective against water-borne pathogens.

Potable Aqua is the clear winner when it comes to speed. Water treated with those tablets is ready to drink 35 minutes after treatment begins. The Micropur tablets take a full four hours to achieve their maximum disinfecting action. One final thought to consider are the side effects.

The toxicity and flavor of iodine can be a little problematic. The iodine tablets are generally not a good choice for pregnant women or anyone with thyroid issues or shellfish allergies. Picky children are also notorious for failing to drink the iodine-infused water, which could lead to dehydration and other serious repercussions in an already dicey emergency. The Katadyn product is chlorine based, most of which dissipates over the allotted four-hour waiting period, so that product is widely tolerated and tastes much better.

To summarize, the Katadyn Micropur tablets cost more and take longer to work, but they last longer and are widely tolerated. Potable Aqua’s iodine tablets are cheaper and work faster, but taste worse and don’t store as long.

bleach for water purification

Household Chemicals

Either bleach or iodine can be carefully used to disinfect water with good results.

Either bleach or iodine can be carefully used to disinfect water with good results. Generally speaking, the amount of the chemical you use will depends on the water quality and temperature. Cold or murky water needs a little more disinfectant (four drops per quart) than warm or clear water (two drops). After adding the chemical, put the lid back on your water container and shake it for a minute. Then turn the bottle upside down, and unscrew the cap a turn, or two. Let a small amount of water flow out to clean the bottle threads and cap. Screw the lid back on tight, and wipe the exterior of the bottle to get the chlorine on all surfaces. Set the bottle in a dark place, or at least in the shade, and let it sit for 30 minutes if the water is clear and at room temperature. When you open the bottle after the allotted time, it should smell like chlorine. If not, add another drop or two and wait another 30 minutes. Don’t take chances or shortcuts with water safety. The last thing you need in an emergency is dysentery.

You can also use the two common forms of iodine to disinfect your water. Iodine is a more harmful substance than bleach in most people’s bodies, but it is an option. To use iodine, it is critical to identify which type you are using. Tincture of iodine 2% is actually much stronger than 10% povidone-iodine solution. Use 5 to 10 drops of tincture of iodine 2% in one quart of water and allow it to sit in the shade for 30 minutes. Again, flush the threads and wipe down the bottle. Use 5 drops for clear or warm water, and up to 10 for cold or cloudy water. Since 10% povidone-iodine solution is weaker, you’ll need 8 to 16 drops per quart of water. Again, use fewer drops for nice looking water and 16 drops for swamp water. Clean the bottle and wait. An added benefit to iodine products is that you can use them for wound disinfections too. Chlorine does not serve double duty like this, and you should never put bleach on any wounds. Never blend iodine and chorine for water disinfection.

cork filter

Build Your Own Filter

This type of filter has some humanitarians looking hard at conifer wood as a readily available material for water filtration devices in developing nations.

We’ve all seen the survival books displaying a water filter made from charcoal-filled pants hanging from a tripod. Sorry to burst your bubble, but that is not a reliable system. It will screen out larger particles, but don’t expect bacteria-free and virus-free water to shoot from this contraption. What could work, however, is a filter made from some flexible hose, glue, and a chunk of pine sapwood. The sapwood’s structure already performs a filtering action in the living wood, screening out air bubbles from the tree sap. Unchecked, these air bubbles would lead to tissue damage.

This type of filter has some humanitarians looking hard at conifer wood as a readily available material for water filtration devices in developing nations. Researchers have successfully used a one-cubic-inch block of pine sapwood as a water filter. (Click here to see their research article.) This chunk of wood was attached to a water supply by using a PVC pipe and some epoxy to prevent water from bypassing the wood filter. Flow rates of several quarts a day were reached in their trials, and E. coli was eliminated by 99.9 percent. These are the same numbers you’ll see from straw-style water filters. Though the wood might allow viruses to pass through (since they are much smaller than bacteria), some water filtration is better than none.

drinking glass of water

Drink It Raw

It’s better to be alive and sickened with pathogens, than dead and pathogen free.

Drinking raw water is certainly a gamble. Even in pristine wilderness areas, the water can be contaminated with all kinds of bowel churning pathogens. Unless you are lucky enough to find a spring that is issuing clean water out of the natural water table, drinking unprocessed water is risky at best. If there’s any way to process the water, it should be attempted before you say “bottoms up” to unprocessed water. But there are always exceptions. If death from dehydration is near, and you cannot treat the water, drink it anyway. It’s better to be alive and sickened with pathogens, than dead and pathogen free.

A water bottle survival kit.
Choose a wide-mouth bottle for easy removal of the items. Outdoor Life Online Editors

Bonus: Build a Water Bottle Survival Kit

A bottle of water can be a valuable commodity to a thirsty person, but it’s not just the water that has worth; the bottle itself can serve many purposes. One of the best uses is as a container for a survival kit. Whether you choose a plastic or metal bottle, here are some items to toss inside.

The Gear

The guts of your water bottle survival kit can be complex and diverse, or down to business. Whatever you stock in the kit, it’s a good idea to include a fair bit of redundancy. Back-ups are always a smart idea when your life may depend on such a small assortment of equipment.

  1. Folding knife and/or mini multitool
  2. Liquid-filled button compass
  3. Small LED flashlight or squeeze light with a spare set of batteries
  4. Bic lighter, ferrocerium rod, and tinder tabs
  5. 40 water purification tablets
  6. Signal mirror and whistle
  7. A space blanket
  8. A Fresnel magnifying lens (back-up fire starter)
  9. 50 feet of 550 cord
  10. Fishing kit, including: 30 yards of monofilament line, 10 bait keeper hooks of various sizes, and split shot
  11. 4 steel safety pins—2 large and 2 small
  12. Small first aid kit
  13. Several feet of Duct tape (could be wrapped around the bottle itself)
  14. A small pouch to hold all of this gear when the bottle is being used to hold liquid

The Bottle

One of the best pieces of gear to hit the outdoor marketplace in recent years is the stainless steel, single-wall water bottle. This rugged vessel is not only crack-proof and crush-resistant, but it can be used to boil your water to make it safe to drink. Important note: If you are using a metal bottle to boil water, the bottle needs to be made of either single-wall stainless steel or some other fire-friendly metal, like titanium, with no paints or coatings. Do not put an insulated bottle or double-wall bottle in the fire. The heat won’t go through properly, and the vessel will probably explode. Skip the aluminum bottles,too, as the metal and the coatings can leach bad stuff into your water.

If you go the plastic route, choose a wide-mouth bottle for easy removal of the items. Also, make sure the bottle is made of Lexan plastic, which can handle higher temperatures without melting, and add a metal cup that fits over the bottle. This gives you the boiling option in an easy and versatile contain

from:    https://www.outdoorlife.com/survival-skills-ways-to-purify-water/

Aspartame – Not So Sweet After All

Top Sweetener Officially Declared a Carcinogen

Analysis by Dr. Joseph MercolaFact Checked
aspartame carcinogenic effects

STORY AT-A-GLANCE

  • The World Health Organization has finally gotten around to declaring the popular artificial sweetener aspartame a potential carcinogen
  • The ruling comes from sources with WHO’s International Agency for Research on Cancer (IARC), who said aspartame will be listed as “possibly carcinogenic to humans” in July 2023
  • I’ve been warning about aspartame’s cancer-causing potential since 2010, so you can see just how long this danger has been known
  • For over a decade, researchers have been warning of aspartame’s neurotoxicity and carcinogenicity, stating reevaluation of aspartame consumption is “urgent and cannot be delayed”
  • A 2022 large-scale cohort study found people who consumed higher levels of artificial sweeteners had higher risk of overall cancer compared to non-consumers

The World Health Organization has finally gotten around to declaring the popular artificial sweetener aspartame a potential carcinogen.1 I warned about aspartame’s cancer-causing potential on my site over 25 years ago, in my best-selling book, “Sweet Deception: Why Splenda, NutraSweet, and the FDA May Be Hazardous to Your Health,” in 2006, and in an article I wrote for The Huffington Post.2 It’s since been deleted — but you can see just how long this danger has been known.

The ruling comes from sources with WHO’s International Agency for Research on Cancer (IARC), who said aspartame will be listed as “possibly carcinogenic to humans” in July 2023.3 Additional findings from the Joint WHO and Food and Agriculture Organization’s Expert Committee on Food Additives (JECFA), which is in the process of updating its aspartame risk assessment, are also expected.4

Donald Rumsfeld’s Hand in Aspartame’s Approval

JECFA has vouched for aspartame’s safety for decades, stating since 1981 that it’s safe when consumed within accepted daily limits.5 It was 1981 when the U.S. Food and Drug Administration first approved aspartame.6 At the time, the late Donald Rumsfeld, former U.S. secretary of defense, was chairman of G.D. Searle, aspartame’s manufacturer, and he was reportedly instrumental in its approval.

At a 1980 FDA Board of Inquiry, the FDA had refused to approve aspartame due to concerns that it could induce brain tumors.7 The late John Olney, a renowned neuroscientist who tried to prevent aspartame’s approval, also wrote a letter to the Board of Inquiry in 1987, warning of aspartame’s neurotoxicity, including the potential for brain tumors and damage to children’s brains.8 As reported by Rense.com:9

“The FDA had actually banned aspartame based on this finding, only to have Searle Chairman Donald Rumsfeld … vow to ‘call in his markers,’10 to get it approved.

On January 21, 1981, the day after Ronald Reagan’s inauguration, Searle re-applied to the FDA for approval to use aspartame in food sweetener, and Reagan’s new FDA commissioner, Arthur Hayes Hull, Jr., appointed a 5-person Scientific Commission to review the board of inquiry’s decision.

It soon became clear that the panel would uphold the ban by a 3-2 decision, but Hull then installed a sixth member on the commission, and the vote became deadlocked. He then personally broke the tie in aspartame’s favor.

Hull later left the FDA under allegations of impropriety, served briefly as Provost at New York Medical College, and then took a position with Burston-Marsteller, the chief public relations firm for both Monsanto and GD Searle.”

Aspartame’s Cancer Link Known for Decades

Despite aspartame’s approval, by 1987 a series of investigative reports raised concerns that the chemical’s approval was mired by conflicts of interest, poor quality industry-funded research and revolving-door relationships between the FDA and the food industry.11

By 1996, a team with the department of psychiatry at Washington University Medical School questioned whether increasing brain tumor rates had an aspartame connection. “An exceedingly high incidence of brain tumors” has been identified in aspartame-fed rats compared to rats not fed aspartame, they explained, adding:12

“Compared to other environmental factors putatively linked to brain tumors, the artificial sweetener aspartame is a promising candidate to explain the recent increase in incidence and degree of malignancy of brain tumors.”

Then, in 2006, a study led by Dr. Morando Soffritti, a cancer researcher from Italy who’s the head of the European Ramazzini Foundation of Oncology and Environmental Sciences, found that, even in low doses, animals were developing several different forms of cancer when fed aspartame.13

That year, the team concluded aspartame was a “multipotential carcinogenic agent, even at a daily dose of 20 mg/kg body weight, much less than the current acceptable daily intake” and stated a reevaluation of aspartame consumption was “urgent and cannot be delayed.”14

A 2007 follow-up study confirmed the findings of aspartame’s “multipotential carcinogenicity,” even at doses close to the acceptable daily intake for humans. Further, it also demonstrated that when lifespan exposure beginning in utero was assessed, aspartame’s “carcinogenic effects are increased.”15 In 2010, Soffritti and colleagues again warned that aspartame was a carcinogenic agent in rats and mice.16

Research Supporting Aspartame’s Carcinogenicity Is Widespread

These studies were only the beginning of the evidence showing aspartame’s cancer-causing potential. In 2012, Harvard researchers published a study in The American Journal of Clinical Nutrition, which found:17

“In the most comprehensive long-term epidemiologic study, to our knowledge, to evaluate the association between aspartame intake and cancer risk in humans, we observed a positive association between diet soda and total aspartame intake and risks of NHL [non-Hodgkin lymphoma] and multiple myeloma in men and leukemia in both men and women.”

Adding further concerns over aspartame’s safety, U.S. Right to Know reported:18

“In a 2014 commentary in American Journal of Industrial Medicine,19 the [Cesare] Maltoni [Cancer Research] Center researchers wrote that the studies submitted by G. D. Searle for market approval ‘do not provide adequate scientific support for [aspartame’s] safety.

In contrast, recent results of life-span carcinogenicity bioassays on rats and mice published in peer-reviewed journals, and a prospective epidemiological study, provide consistent evidence of [aspartame’s] carcinogenic potential.’”

A 2020 study further supports the Ramazzini Institute’s (RI) original findings, revealing a statistically significant increase in total hematopoietic and lymphoid tissue tumors (HLTs) and total leukemias and lymphomas in female rats exposed to aspartame.

“After the HLT cases re-evaluation, the results obtained are consistent with those reported in the previous RI publication and reinforce the hypothesis that APM [aspartame] has a leukemogenic and lymphomatogenic effect,” the researchers explained.20

Again in 2021, a review of the Ramazzini Institute data further confirmed that aspartame is carcinogenic in rodents. The researchers noted that their findings “confirm the very worrisome finding that prenatal exposure to aspartame increases cancer risk in rodent offspring. They validate the conclusions of the original RI studies.”21

In response, they called on national and international public health agencies to reexamine aspartame’s health risks, particularly prenatal and early postnatal exposures.22

WHO Warns Against Artificial Sweeteners for Weight Control

Aspartame’s cancer link is especially concerning given its prevalence in diet foods and drinks. Aspartame is used in 1,400 food products in France and more than 6,000 products around the globe. The chemical is commonly found in food products such as sugar-free gum, diet drink mixes and sodas, reduced-sugar condiments and tabletop sweeteners, including Equal and NutraSweet.26

Its high level of sweetness — 200 times greater than sugar27 — and low calories makes it popular among people looking to make their drinks and meals sweeter without the calories of a comparable amount of sugar.

But, in addition to labeling the artificial sweetener as possibly carcinogenic, in May 2023, even the beyond-corrupted WHO released a guideline advising not to use non-sugar sweeteners (NSS) for weight control because they don’t offer any long-term benefit in reducing body fat in adults or children.28

Previously, WHO conducted a systematic review and meta-analysis that revealed “there is no clear consensus on whether non-sugar sweeteners are effective for long-term weight loss or maintenance, or if they are linked to other long-term health effects at intakes within the ADI.”29

The systematic review also suggested “potential undesirable effects from long-term use of NSS, such as an increased risk of type 2 diabetes, cardiovascular diseases, and mortality in adults.” Even cancer was called out in analysis, which included 283 studies and found artificial sweeteners are linked to an increased risk of:30

Obesity Type 2 diabetes
High fasting glucose All-cause mortality
Cardiovascular events Death from cardiovascular disease
Stroke High blood pressure
Bladder cancer Preterm birth and possible adiposity in offspring later in life

Further, according to the WHO study:31

“Mechanisms by which NSS as a class of molecules might exert effects that increase risk for obesity and certain NCDs [non-communicable diseases] have been reviewed extensively and include interaction with extra-oral taste receptors, possibly with alteration of the gut microbiome.

Because sugars and all known NSS presumably elicit sweet taste through the TAS1R heterodimeric sweet-taste receptor, which has been identified not just in the oral cavity but in other glucose-sensing tissues, it is not surprising that such a group of vastly different chemical entities could be responsible for similar effects on health.”

from:    https://articles.mercola.com/sites/articles/archive/2023/07/14/aspartame-carcinogenic-effects.aspx?ui=f460707c057231d228aac22d51b97f2a8dcffa7b857ec065e5a5bfbcfab498ac&sd=20211017&cid_source=dnl&cid_medium=email&cid_content=art1ReadMore&cid=20230714_HL2&foDate=true&mid=DM1432971&rid=1855621420

We’re Saving You A Trip!!!

Gates, WHO Envision Future Where ‘Vaccine Patches Could Be Mailed Directly to Peoples’ Homes’

A new vaccine technology that delivers vaccines through microneedles on patches is known as vaccine microarray patches (VMAP). It is backed by global players including the World Health Organization (WHO) Gavi, the Vaccine Alliance and the Bill & Melinda Gates Foundation. The patches have yet to be approved by regulators, but are still being promoted. VMAPs are easier to deliver, especially to children, than traditional needle jabs. The head of the National Vaccine Information Center said that vaccine ‘hesitancy’ “has never been about how the product is delivered.” Instead, “it has always been about the lack of evidence demonstrating safety.”

.A new vaccine technology using patches instead of needles is being described as “groundbreaking,” a “game changer” and having the potential to “transform immunisation coverage in lower-income countries.”

Backed by global players including the World Health Organization (WHO) Gavi, the Vaccine Alliance and the Bill & Melinda Gates Foundation, among others, vaccine-containing microarray patches (VMAP) — also known as “micro-array patches” or “microneedle patches,” have been the subject of dozens of scientific papers in recent years.

The claimed benefits of such “vaccine patches” — for everything from measles and rubella (MR) vaccines to various mRNA vaccines — are being widely promoted even though few clinical trials have been completed and no such vaccine has yet been approved by regulators.

Scientific and medical experts who spoke with The Defender raised questions about the technology and warned of potential dangers.

Barbara Loe Fisher, co-founder and president of the National Vaccine Information Center and co-author of the 1985 book “DPT: A Shot in the Dark,” told The Defender:

“Whether it is delivered by a needle or a patch, a VMAP is a biological product that atypically manipulates the immune system to provoke strong inflammatory responses that can lead to injury or death for some who receive it.

“If you look at the medical literature describing microneedle vaccine patches, what you see is a lot of hype about how much easier it will be for the vaccinators to slap a patch on a child’s skin instead of using a needle, and how the ‘painless’ patch can reduce vaccine hesitancy.”

Fisher said vaccine hesitancy “has never been about how the product is delivered.” Instead, “it has always been about the lack of evidence demonstrating safety.”

Brian Hooker, Ph.D., P.E., senior director of science and research for Children’s Health Defense, said that the term “vaccine patch” may also be misleading, as it might be confused with nicotine patches for smokers.

Hooker told The Defender:

“The term ‘vaccine patch’ is misleading in that this microarray technology is nothing like other patch-based delivery systems for nicotine or hormones. This ‘patch’ still breaks the skin in order to deliver the liquid vaccine that is contained in the microarray’s matrix.

“As such, I don’t quite understand how this injection system will be delivered to patients and parents to administer the vaccine directly. That seems quite risky.

“Unfortunately, repackaging the same vaccines in this different platform does nothing to improve their safety — as this seems more a ploy to convince consumers otherwise.”

VMAP backers seek to ‘turn vaccines into vaccinations’

VMAPs can “overcome many obstacles and bottlenecks faced by intradermal vaccine delivery, thus maximising the reach of vaccines to the most remote locations to turn vaccines into vaccination,” according to an article published last week by Gavi.

According to UNICEF, “VMAPs can increase vaccine coverage by increasing acceptability by caregivers and recipients, and administering vaccines more rapidly and easily with minimally trained health care workers” and can “substantially improve the productivity and resilience of governments to expand immunization coverage.”

UNICEF’s position mirrors that of the WHO, the Gates Foundation and the Clinton Health Access Initiative — “The Big Catch-up” — described as “the largest childhood immunization effort ever,” intent on reversing “declines in childhood vaccination recorded in over 100 countries since the pandemic.”

UNICEF said it is “focusing on driving the research, development and scale of VMAPs,” including “identifying barriers for scaling and investigating the need for market pull incentives to spark interest and endorsement by vaccine manufacturers.”

Nevertheless, no VMAPs have yet been approved by regulators, according to Gavi, which states that, at present, “one measles and rubella vaccine patch has completed Phase 1/2 clinical trials. Two additional phase 1/2 clinical trials are planned.”

“Some COVID-19 and flu vaccines are also entering Phase 1/2 trials, and other vaccines such as HPV are undergoing preclinical assessment,” Gavi added.

According to Gavi, data from Phases 1 and 2 of the first-ever clinical trial of VMAPs in children was shared in May during the Microneedles 2023 conference in Seattle and delivered “promising results.”

The trial, conducted in Gambia with 45 adults, 120 toddlers 15-18 months of age, and 120 infants 9-10 months of age, “evaluated the safety, immunogenicity, and acceptability” of an MR vaccine delivered by micro-array technology developed by Atlanta-based Micron Biomedical.

The vaccine itself was developed by the Serum Institute of India, the world’s largest vaccine manufacturer by number of doses produced and sold. The Serum Institute produces the COVISHIELD COVID-19 vaccine, as well as over half of the world’s vaccines administered to babies.

The Serum Institute, along with Bill Gates, are named as defendants in a pair of lawsuits filed by family members of deceased vaccine injury victims in India.

Envisioning a future where ‘vaccine patches could be mailed directly to peoples’ homes’

The lack of any successfully completed clinical trials has not stopped the proponents of VMAPs from claiming this technology will deliver a broad range of benefits.

According to Gavi, VMAPs are “needle-free and pre-dosed,” simplifying the administration of vaccines, which can then “be carried out by minimally trained volunteers.”

Gavi also claims VMAPs “are safer as they overcome the risks related to operational errors” during administration, such as dosage errors and needle-stick injuries.

VMAPs are “easier to distribute,” according to Gavi, due to their light weight and “enhanced thermostability” which addresses “the problem of vaccine storage requirements” and removes “the need for cold-chains.”

Moreover, Gavi claims “The lower level of pain experienced during administration with MAPs would help reduce vaccine hesitancy and increase vaccine acceptability.”

“There are difficulties in reaching the last mile with the current injectable vaccines since they depend on a functional cold-chain and administration by well-trained staff … Furthermore, most vaccines are administered via injection that may cause pain, and discomfort that leads to hesitancy,” UNICEF states.

Healthcare consulting firm Avalere said VMAPs provide “the potential for lower healthcare costs,” “increased compliance due to convenient and pain free application,” are “ideal for patients with needlestick phobias or difficulty swallowing,” and are “easier for children, older people and patients requiring complex care.”

According to CEPI, VMAPs “could enable a future in which vaccine patches could be mailed directly to peoples’ homes, workplaces and schools, avoiding the delay and inconvenience of traditional needle-and-syringe vaccine scheduling and administration.”

CEPI describes itself as “an innovative global partnership between public, private, philanthropic, and civil society organisations launched in Davos in 2017 to develop vaccines to stop future epidemics.”

VMAPs proposed for wide range of vaccines, including mRNA injections

Proponents of VMAP say the purported benefits of this technology can ultimately translate to acting as an “advantageous delivery route for existing vaccines,” including influenza, tetanus toxoid, MR, hepatitis B and “biologics and small molecules.”

According to the WHO, a VMAP for the MR vaccine may be “potentially favourable,” with “perceived operational advantages that could ultimately increase equitable coverage and facilitate vaccine administration in inaccessible areas.”

For the same vaccine, a Jan. 16 article in the Frontiers in Public Health journal states that as vaccination coverage for measles and rubella “has stagnated,” VMAPs “are anticipated to offer significant programmatic advantages to needle and syringe” options and lead to increased vaccination coverage, with “significant demand expected for MR-MAPs between 2030 and 2040.”

And on Jan. 17, CEPI launched preclinical testing for a “high-density microarray patch … to assess its stability, safety and immunogenicity and to evaluate its potential as a rapid-response technology for heat-stable, dried-formulation mRNA vaccines.”

According to CEPI, this initiative was borne out of its January 2022 call for proposals, as part of its “wider strategic goal of harnessing innovative technologies to improve the speed, scale and access of vaccine development and manufacturing in response to epidemic and pandemic threats.”

Gates, World Bank, World Economic Forum connected to VMAP proponents

While Gavi states that “There is a need for investments to fund pilot-scale manufacturing facilities” for VMAPs, Gavi and other entities that are actively promoting this technology are themselves backed by or connected to some of the world’s most prominent investors, as well as major global organizations.

Gavi says it “helps vaccinate almost half the world’s children against deadly and debilitating infectious diseases.” It was established in 1999, with the Gates Foundation as one of its co-founders and one of its four permanent board members.

Gavi maintains a core partnership with UNICEF, the World Bank and the WHO, which includes Gavi in its list of “relevant stakeholders,” while the Rockefeller Foundation also is a partner and board member — and donor — to Gavi.

Gates-related connections extend to PATH president and CEO Nikolaj Gilbert, who is a member of Challenge Seattle, described as “an alliance of CEOs from Seattle area’s largest employers including Microsoft, Bill & Melinda Gates Foundation, Starbucks, and Boeing.” He previously served as director for Big Pharma firm Novo Nordisk.

According to PATH’s 2021 annual report, the organization is funded by organizations including the Gates Foundation, the Schwab Charitable Fund and the Vanguard Charitable Endowment, in addition to the United Nations, Gavi, the Centers for Disease Control and Prevention, the World Bank and the WHO.

PATH has also received funding from the Gates Foundation, the Rockefeller Foundation, Google and the World Bank for vaccine projects in countries such as India.

The Gates Foundation is also a co-founder of CEPI, along with the Wellcome Trust and the World Economic Forum (WEF). Indeed, CEPI was founded in Davos, Switzerland — home of the WEF’s annual meeting. Its CEO, Dr. Richard J. Hatchett, was previously acting director of the U.S. Biomedical Advanced Research and Development Authority.

Several CEPI board members are also connected to entities like the Gates Foundation.

For instance, Dr. Anita Zaidi is the president of gender equality, director of vaccine development and surveillance, and director of enteric and diarrheal diseases programs at the Gates Foundation, while non-voting member Gagandeep “Cherry” Kang, M.D., Ph.D., is chair of the foundation’s Joint Working Group.

Νon-voting member Dr. Juan Pablo Uribe is the global director for Health, Nutrition and Population and director of the Global Financing Facility for Women, Children and Adolescents at the World Bank.

Dr. Mike Ryan, also a non-voting member, is the executive director of the WHO’s Health Emergencies Programme who gained global prominence during the COVID-19 pandemic through his participation in WHO briefings.

And non-voting member Dr. L. Rizka Andalucia is the director-general for Pharmaceutical and Medical Devices at Indonesia’s Ministry of Health. In November 2022, Indonesian Minister of Health Budi Gunadi Sadikin, at the G20 meeting in Bali, called for a “digital health certificate acknowledged by the WHO” that would allow the public to “move around.”

This article was originally published by The Defender — https://childrenshealthdefense.org/defender/bill-gates-who-vaccine-patch-vmap/

from:    https://needtoknow.news/2023/07/gates-who-envision-future-where-vaccine-patches-could-be-mailed-directly-to-peoples-homes/

Just A little Prick: It’s All Good!

(OK:  WAY TOO LONG FOR A QUICK READ, BUT it is time to acknowledge what we are really dealing with and what you want your future and that of your loved ones to be.)

Propaganda-In-Action: How The Media Minimizes mRNA Vaccine Injuries

“Hurt” by ₡ґǘșϯγ Ɗᶏ Ⱪᶅṏⱳդ is marked with CC0 1.0
Propaganda is the Technocrat way of sowing confusion and doubt about what otherwise is self-evident reality. Some people call this “gaslighting”. Whatever you are seeing with your own eyes is miss-interpreted or miss-represented and therefore you should accept the propaganda as being true. This is blatant fraud, but people fall for it time after time, giving the reason why propaganda continues to be sprayed from a firehose. ⁃ TN Editor

I regard consensus science as an extremely pernicious development that ought to be stopped cold in its tracks. Historically, the claim of consensus has been the first refuge of scoundrels; it is a way to avoid debate by claiming that the matter is already settled. Whenever you hear the consensus of scientists agrees on something or other, reach for your wallet, because you’re being had… Let’s be clear: the work of science has nothing whatever to do with consensus. Consensus is the business of politics. Science, on the contrary, requires only one investigator who happens to be right, which means that he or she has results that are verifiable by reference to the real world. In science consensus is irrelevant. What are relevant are reproducible results. The greatest scientists in history are great precisely because they broke with the consensus. There is no such thing as consensus science. If it’s consensus, it isn’t science. If it’s science, it isn’t consensus. Period.

– MICHAEL CRICHTON, LECTURE AT THE CALIFORNIA INSTITUTE OF TECHNOLOGY, PASADENA, CALIFORNIA, JANUARY 17, 2003. (1)

Within a few months of the SARS-Cov-2 vaccines being injected into millions of people, numerous types of adverse reactions were reported throughout the world. Information about adverse events became an object of intense denial and obfuscation by government agencies and state-funded and corporate-sponsored media, whether the information was in the form of rumors, amateur speculation, or serious scientific inquiry by qualified academics.

However, in 2023, government registries of vaccine injuries now reveal serious deficiencies of the vaccines designed to combat SARS-Cov-2. In a report published in the International Journal of Vaccine Theory, Practice, and Research, the authors analyzed data from regulatory surveillance and self-reporting systems in Germany, Israel, Scotland, the United Kingdom, and the United States “to find long-term adverse events of the COVID products that cannot be captured during the expedited safety analyses.” This extract from the abstract goes on to state:

Our data show, among other trends, increases in adverse event reports if we compare COVID products to influenza and pertussis vaccines and statistically significant higher numbers of hospital encounters in military personnel, as well as increases in incidences of thromboembolic conditions, such as menstrual abnormalities, myocarditis, and cerebrovascular events after the implementation of COVID injection mandates, compared to the preceding five years… Our meta-analysis of both national and international vaccine adverse events emphasizes the importance of re-evaluating public health policies that promote universal mass injection and multiple boosters for all demographic groups. In combination with informal reports from reliable witnesses, limitations of the safety trials, and the decreased lethality of new strains, our research demonstrates that the cost (both monetary and humanitarian) of injecting healthy people, and especially children, outweighs any claimed though unvalidated benefits. (2)

In this late phase of the event that started in 2020, governments and their various propaganda platforms cannot hide these adverse events and are now engaged perhaps in what can be called the “cooling the mark out” phase of the pandemic. An article in The New Yorker in 2015 discussed this sociological phenomenon (3). The term was used in a 1952 study by Erving Goffman to describe an important element of con artistry, but it also describes generally any social mechanism that is needed to help people adjust to material losses and humiliation. When a victim is forced to acknowledge he has been conned or ripped off, the perpetrators have to make some effort to help him adjust. Otherwise, he may do something “irrational” such as pursuing violent revenge, media exposure, criminal charges, or a lawsuit. He needs to be reminded that he still has precious things he could lose, so he has to just accept the loss and humiliation and go back to his wife and children. Governments are doing the same now: “Yes, there have been some rare adverse events. Get in line and fill out this form to apply for your legally entitled compensation. We will be with you shortly.”

Some of the adverse events are mild reactions such as fainting, dizziness, fatigue, and flu-like malaise lasting a few days—just like the viral infection itself, ironically enough. People under age seventy who had a 99.9% chance of recovering quickly from the infection chose instead to suffer this malaise, going along with the social coercion and accepting the unknown risks of vaccination (4). As if it were a scheduled elective surgery, they were simply choosing the timing of when they were going to feel horrible—i.e. “I should get this over with now before my vacation.”

The less mild reactions are myocardial infarction, myocarditis, pericarditis, tachycardia, stroke, blood clots (embolism), aneurysm, tinnitus, Bell’s Palsy, Guillain-Barré Syndrome, transverse myelitis, cancer, heavy bleeding, menstrual irregularities, miscarriage, neurological symptoms, immune system disorders, skin rash, intense pain and numbness, memory loss, “brain fog,” and “inexplicable” sudden death. These conditions can be transitory or, like the last one on the list, permanent.

One can easily find peer-reviewed research papers that confirm the increased rates of these adverse health events after vaccination, yet a curious thing about them is that they often end very tentatively, including a phrase such as the one found in the extract below:

The number of reported cases is relatively very small in relation to the hundreds of millions of vaccinations that have occurred, and the protective benefits offered by COVID-19 vaccination far outweigh the risks. (5)

This tendency was also found in the recent Cochrane review on the efficacy of wearing masks (6). Instead of stating emphatically that in numerous studies there is no evidence to show a benefit in wearing masks, the authors concluded by stating all the ways that the studies they reviewed might contain some undiscovered flaws. It was like they were afraid of having made an important discovery that should change government policy.

Minimization, Exaggeration, Diversion and Distraction in Mass Media and Scientific Journals

Example 1: Putting a Positive Spin on Vaccine-Induced Cancer

Another such example, this one in the popular press, was the story told about the immunologist Dr. Michel Goldman in The Atlantic in September 2022 (7). As an advocate of many vaccines during his career, and in particular as a believer in the salutary effects of the mRNA vaccines, he was confronted with the images on a CT scan that showed lymphatic cancer spreading aggressively in his body soon after his mRNA shots, both after the first two shots and then again after a booster shot a few months later. The cancer connection to the shots was hard to deny because the aggressive growth was extremely rare and also because the first shots were in the left arm and the cancer appeared on the left armpit. The booster was injected in the right arm, then the cancer appeared on the right side.

If the subject matter were not so dark, the article would appear to be a satire of people who can’t think logically or change their views when confronted with new facts. The author, Roxanne Khamsi, goes to extreme lengths to describe the struggle she had to write the story in a way that would not lend support to those who spread “anti-vaccine disinformation.” Dr. Goldman was just as determined, willing to see himself as one of the rare unfortunate ones who must suffer so that so many others may be saved by these supposedly miraculous new drugs.

As Piers Robinson’s lessons on propaganda have taught us, the propagandist doesn’t lie directly. Propaganda operates through exaggeration, omission, incentivization and coercion, and these are in evidence in The Atlantic, in this article, and in all of its coverage of the pandemic (8). Roxanne Khamsi selectively focuses on the most hyperbolic reactions from the “fearmongers [who] have made the problem worse by citing scary-sounding data from the Vaccine Adverse Event Reporting System… with insufficient context.” She also had to mention that a vaccination center was set ablaze in Poland. Nowhere in the long article is there any mention of less radical reactions such as the hundreds of scientific papers describing adverse events—studies written by non-fearmongering sober-minded scientists. Such exaggeration and omission move the reader toward an acceptance of the necessity of mass vaccination.

Another facet of this propaganda is its use of what could be called “The New Yorker” genre of journalism. It is a “long read” piece (4,000 words) of narrative storytelling that uses the methods of fictional literature. It dramatizes the story arc of one individual, going deep into his biographical details, thoughts, and feelings. This is the genre that is natural and expected by the educated professional class of people who wake up on Sunday mornings and look for something serious to read, something that will make them feel smart before going back to the grind the next day. It is also a genre used by documentary filmmakers. They may have an important social problem to expose, but they have to find a person at the center of it and tell a story. Otherwise, the audience will tune out. The TED talks tell us it is hardwired in our brains. Humans are storytellers.

The New Yorker genre makes the educated class feel informed and serious: 4,000 words, a deep read, not the superficial stuff that the deplorables read in the New York Post! The length of the piece makes it likely that readers won’t be using their time to read anything else. Most importantly, the use of this genre diverts attention away from the need for an objective understanding of a phenomenon that involves billions of victims. The writer and the subject, Dr. Goldman, say much about the need to understand the science and not inflame radical reactions from the so-called low-information types, but this genre is itself un-scientific, subjective, sentimental, and narrow in its scope.

The most stunning omission in the article is that neither the author nor Dr. Goldman makes the obvious logical conclusion that, considering both the apparent and the still unknown risks, mandatory or coerced vaccination is unethical, especially for a viral infection that 99.9% of people under age seventy can survive. After learning of what happened to Dr. Goldberg, persons in good health, if not propagandized to think otherwise, would logically decide in favor of taking their chances with an infection that will pass in a few days. This is especially true for people who, unlike Dr. Goldman, don’t have a brother who is head of nuclear medicine at a university hospital and may not have timely access to the high quality of health care that Dr. Goldman had.

The article concludes thus:

And as a longtime immunologist and medical innovator, he’s still considering the question of whether a vaccine that is saving tens of millions of lives each year might have put his own in jeopardy. He remains adamant that COVID-19 vaccines are necessary and useful for the vast majority of people.

Many would disagree and say that the vaccines are, at best, only for the non-vast minority of high-risk individuals who accept them with informed consent. Despite his own experience of suffering vaccine-induced aggressive lymphoma, Dr. Goldman believes that a vast majority of people should subject themselves to the risk of suffering the same fate. In September 2022, the time of publication, it had been officially acknowledged that the mRNA shots had not stopped the spread of the virus, had not induced lasting immunity, and may not have lowered the fatality rate of the illness. Other possible explanations:

(1) The virus harmed most of the vulnerable population before the vaccines arrived.

(2) Doctors learned how to treat the disease without resorting to deadly practices such as delayed treatment, ventilators and Remdesivir.

(3) The virus evolved into less deadly variants.

The purported benefits of the vaccines remain unprovable, and explanations (1)-(3) remain as matters of controversy.

Example 2: The Feint After Post-Vaccination Fainting

Other examples of this genre applied to the Covid-19 event are plentiful and easy to find in the media that have been funded by the Bill and Melinda Gates Foundation or sponsored by Pfizer and other hidden hands. I will describe just one more that shows that it was still being used in April 2023, three years on as the official narrative becomes untenable.

On April 10th, 2023, NBC News published a 3,400-word piece on the “fainting nurse” social media frenzy that occurred in December 2020 when frontline healthcare workers in the US started to receive the mRNA shots (9). The vaccination of nurse Tiffany Dover was recorded by a local television news crew because it was the big day when the savior vaccines had arrived to supposedly end the pandemic. Unfortunately, the cameras recorded her fainting shortly after receiving her injection.

The article describes how “conspiracy theorists” created an episode of “participatory misinformation” as they circulated her story on social media, exaggerated what the fainting meant, spread rumors of her death, and engaged in a campaign of harassment (a.k.a. doxing) (10). Tiffany remained steadfastly supportive of the vaccination program and believed that her fainting was inconsequential, yet she was traumatized by the doxing and chose to remain silent for two full years. Unfortunately, this choice only intensified the rumors of her death or of her enforced silence.

My critique of this article includes no support for the people who engage in doxing and wild speculation. My criticism is that this genre of journalism consistently associates all disagreement with the official narratives as the work of wild-eyed, deplorable bullies. It consistently ignores the hundreds of scientists who are publishing peer-reviewed articles on vaccine injuries and questioning the abandonment of standard public health policy that started in 2020.

Brandy Zadrozny, the author of this article about Tiffany Dover, felt it was necessary to associate Tiffany’s story with other instances of unhinged conspiracy theory such as the 2020 election being stolen from Donald Trump and the denial of the murders at Sandy Hook Elementary School. Thus, the very intentional implication here is that if you are concerned about the accumulation of medical journal articles describing a long list of vaccine-related injuries, think twice. You don’t want to be dismissed as one of those cruel and deranged fools who have lost touch with reality. Your family, friends and colleagues are all being trained to ostracize you for wrongthink, so forget about it. You are the mark that needs to be cooled out.

Instead of treating the “participatory misinformation” campaign as a problem of the deplorables that the righteous must struggle to solve, the writers of such articles could start to wonder if there is some legitimate anger driving such regrettable phenomena. There were very sound reasons to worry about a pharmaceutical product being rushed to market in less than a year, especially one that was based on a novel biotechnology. Additionally, fainting, after all, is not always a minor incident, and it is rational to be concerned about it happening so soon after a medical treatment. Furthermore, it would not be unreasonable for a healthy person to decide he would rather risk infection with the virus than suffer side-effects from an unproven vaccine. Not everyone has the good fortune to faint “into the arms of two nearby doctors” (as the fainting was described in the article). Some people break bones and sustain skull fractures. Some people have their adverse reaction after they leave the clinic and are driving home. Some have it months later.

After more than two years since vaccinations began, it should have been clear that, because the mRNA treatments were not as safe and effective as promised, no one should have ever been coerced into taking them. Their heavy promotion, backed by well-funded propaganda campaigns of half-truths and bold lies, was unethical, as was the gaslighting, shaming and shunning of the people who demanded bodily autonomy.

However, at this late date, after so much has been officially admitted about the adverse effects, including death, the author claimed that Tiffany’s story became a rallying point for those “who falsely believe that vaccines are killing and injuring people in droves.” (italics added) Those last two words were probably chosen carefully because without them one could not say they “falsely believe.” It is a fact that they are killing and injuring people, but “in droves” may be ambiguous enough to make the statement passable for a quibbling fact checker. The sentence is now “partially true” if one wants to see it that way.

One can denounce the campaign of coercion and still let Tiffany have her proclaimed “belief” in the vaccines. The issue that should be discussed is the failure of medical ethics in public policy that led to the vilification of people who had a different belief. They did not want to submit themselves to a medical therapy that had been rushed to market with no long-term safety data to support its use. Despite the facts, this issue remains utterly invisible to the writers who specialize in this genre.

The final thing to mention about this article is that, like the article in The Atlantic, it uses the devices of fiction. It focuses on the emotional and physical condition of the subject and thus leads the reader to an engagement with her story. Her eyes are “wide and bright and terribly blue.” They are described again at the end of the article as “electric blue.” The writer emphasizes this because a post-vaccination photo of her was not lit well and her eye color was not visible, and this is what set off rumors that it was not really her in the photo. Nonetheless, the descriptions are unnecessary embellishments. Readers don’t need to know her hair dye choices, either, but these too were described. This news article about a controversial pharmaceutical product could also be reported without the accompanying glamor photos of the very photogenic victim. There are, after all, less glamorous and less fortunate victims of vaccination who suffered fates worse than fainting (11). Tiffany is alive and healthy, and she did not refuse to be filmed on the day of her vaccination. This isn’t really about a story about her fainting and its aftermath, however. The purpose of this genre is the feint—the fake out and distraction from what the public should really be paying attention to.

Example 3: Minimization in Scientific Journal Articles

Let’s return to the scientific journal articles. Concluding statements in scientific papers are not always about objective findings. They are interpretations and opinions by the authors, and they often seem to go in the direction of minimizing the problems revealed by the study. It has always been standard practice for researchers to be humble about the impact of their work, for their conclusions may be disproven by subsequent research. Nonetheless, when it comes to any research related to Covid-19, excessive hesitancy and even fear are evident.

For some reason, the medical specialists authoring these papers never express alarm or suggest a halt to vaccination of individuals who are at low risk of suffering serious harm from the viral infection. Recall that the infectious mortality rate was found to be about 0.1%, more or less, depending on one’s age. It is this low for healthy individuals and higher for the elderly and the unhealthy. As mentioned above, the rate became lower as doctors learned how to treat the infection and abandoned dangerous interventions. Another factor was the virus itself becoming less deadly.

Readers might respond that I am ignoring the millions of cases of “long covid,” but my response is that there is no clinical definition for it, and it may be no different than the post-viral syndrome associated with influenza—a phenomenon which never aroused alarm in society before 2020. The alleged symptoms of long covid also overlap with adverse reactions to the vaccine, so if we must be concerned about long covid, we also have to object to the continued use of therapies that use the spike protein to induce immunity. Doctors are developing treatments for reactions to the spike protein, whether they came from the virus or the mRNA jabs. It is also likely that “long covid” is a side effect of “long type 2 diabetes” and various other chronic (i.e. long duration) illnesses that are the root causes of death by SARS-Cov-2.

The ritualistic minimization of vaccine injuries in the scientific reports is obviously an essential bow of fealty to the scientific priesthood. It is the modern equivalent of Galileo in the 17th century affirming the existence and greatness of God in order to, hopefully, have heliocentrism taken seriously. These researchers may feel privately that the matter is urgent, but they know that in order to shine any light on the issue in a respected medical journal, they will have to bow down to the official doctrine. They justify it as the only way to shine some light on the problem and change the system from within. If they really thought the matter was so trivial, they wouldn’t study it. Medical personnel could just treat their patients without worrying about the speculative role vaccines might have played in their illnesses. A doctor treating a cancer rarely worries about whether it was caused by fallout from nuclear weapons testing because identifying this cause would make no difference in the treatment. Her job is to treat the patient. However, in the late 1950s, some doctors saw a reason to speak out and create the political pressure that halted nuclear tests in the atmosphere in 1963.

The paper cited in the appendix below, to conclude this long essay, was chosen as an example of this minimization. It is concerned with liver diseases following vaccination. I found this one because recently I took note of the 15th mRNA-jabbed person in my social circles to suffer a severe health crisis since January 2021. In the two years before then, I knew of only one medical emergency among friends, family, and colleagues. In the 15th person’s case, it was a pyogenic liver abscess that put him in the ICU and almost killed him.

In studies like this that conclude by minimizing the problem, there is an obvious problem in saying the number of cases is “very small in relation to the hundreds of millions of vaccinations.” When one considers all of the research on adverse events in all other organ systems, one starts to think, as Yogi Berra said, “Little things are big.” Yogi Bear was smarter than the average bear, and Yogi Berra, the “dumb” sage of baseball legend, was, it seems, far smarter than the average immunologist. Little things do start to add up. One case of lymphoma, or fainting, or liver disease may seem insignificant when seen is isolation, but when all the adverse events are seen together from a distance, along with a sharp rise in all-cause mortality, we can start to ask the right questions (12). They are similar to the questions we should ask about the compounding effects of numerous environmental toxicants and pollutants humans are exposed to. One chemical might be declared safe at a certain exposure, but what is the combined effect of hundreds of such chemicals? It looks like the harms are extremely rare only when cases and types of injuries are studied in isolation and the victims are also kept isolated.

We could also add Yogi Berra’s other gems of wisdom that apply to the entire Covid phenomenon. When we find that not much has changed since Galileo’s time, recall that Yogi Berra said, “it’s like déjà vu all over again,” and when you think about all that has happened since March 2020, remember he said, “the future ain’t what it used to be.”

References


  1. J.R. Barrio, “Consensus science and the peer review.” Molecular Imaging and Biology. April 2009, 11(5): 293. doi: 10.1007/s11307-009-0233-0. PMID: 19399558; PMCID: PMC2719747.
  2. E. Romero, S. Fry, S., and B. Hooker, “Safety of mRNA Vaccines Administered During the First Twenty-Four Months of the International COVID-19 Vaccination Program,” International Journal of Vaccine Theory, Practice, and Research, 2023, 3(1), 891–910. https://doi.org/10.56098/ijvtpr.v3i1.7
  3. Louis Menand, “Crooked Psychics and Cooling the Mark Out,” The New Yorker, June 18, 2015. “The classic exposition of the practice of helping victims of a con adapt to their loss is the sociologist Erving Goffman’s 1952 article ‘On Cooling the Mark Out.’ … ‘After the blowoff has occurred,’ Goffman explained, about the operation of a con, ‘one of the operators stays with the mark and makes an effort to keep the anger of the mark within manageable and sensible proportions. The operator stays behind his team-mates in the capacity of what might be called a cooler and exercises upon the mark the art of consolation. An attempt is made to define the situation for the mark in a way that makes it easy for him to accept the inevitable and quietly go home. The mark is given instruction in the philosophy of taking a loss.’ What happened stays out of the paper.”
  4. Angelo Maria Pezzullo, Cathrine Axfors, Despina G. Contopoulos-Ioannidis, Alexandre Apostolatos, John P.A. Ioannidis, “Age-stratified infection fatality rate of COVID-19 in the non-elderly informed from pre-vaccination national seroprevalence studies,” Environmental Research, January 2023. This study found that Covid-19’s infection fatality rate (IFR) by age was under 0.1% for those under 70. The breakdown by age was 0.0003% at 0-19 years, 0.003% at 20-29 years, 0.011% at 30-39 years, 0.035% at 40-49 years, 0.129% at 50-59 years, and 0.501% at 60-69 years.
  5. S. Alhumaid et al., “New-onset and relapsed liver diseases following COVID-19 vaccination: a systematic review.” BMC Gastroenterology, October 2022; 22(1):433. doi: 10.1186/s12876-022-02507-3. PMID: 36229799; PMCID: PMC9559550. The abstract states, “Mortality was reported in any of the included cases.” Was the erroneous use of any in this sentence a typographical error or a deliberate ambiguity put into the abstract? There are three options for a correct interpretation: 1. Mortality was not reported in any of the included cases… 2. Mortality was reported in many of the included cases… 3. Mortality was reported in all of the included cases. It is difficult to know the authors’ intended meaning regarding this significant finding from their research. The sample sizes (six figures indicated as sample sizes, n=x) total 41 cases out of the 275 cases studied. This is a fatality rate of 15%, but it is difficult to know what the intended meaning of the 32 authors is, due to the ambiguity described above. One can conclude that any ofmany ofall of, or not any of the authors read the abstract carefully before it went to press. In any case, even if there were no deaths, one could take issue with the statement that “patients were easily treated without any serious complications, recovered and did not require long-term hepatic therapy.” Many patients would not feel so optimistic about having had such damage inflicted on a vital organ which is, considering the contemporary food supply and environment, already exposed to enough harm.
  6. Tom Jefferson et al., “Physical Interventions to Interrupt or Reduce the Spread of Respiratory Viruses,” Cochrane, January 30, 2023.
  7. Roxanne Khamsi, “Did a Famous Doctor’s COVID Shot Make His Cancer Worse? A Lifelong Promoter of Vaccines Suspects He Might Be the Rare, Unfortunate Exception.” The Atlantic, September 24, 2022.
  8. “David Miller and Piers Robinson, Propaganda—An introduction by David Miller and Piers Robinson.” YouTube Channel. (3:25~), accessed April 15, 2023.
  9. Brandy Zadrozny, “Conspiracy theorists made Tiffany Dover into an anti-vaccine icon. She’s finally ready to talk about it,” NBC News, April 10, 2023.
  10. It is important to note that this phenomenon has many precedents that occurred long before social media existed. The Dreyfus Affair (1890s) and the death of Azaria Chamberlain in Australia (1980) are just two examples one could refer to. The latter one was the butt of several jokes in poor taste broadcast on mainstream media outlets (referencing the apocryphal phrase “A dingo ate my baby!”) Back then, the incident was referred to benignly by the mass media as a regrettable “media circus.” The panic in the mainstream media about the new panics is interesting in the way it views professional journalism as beyond reproach and “participatory misinformation” as an urgent new threat posed by irresponsible, out-of-control social media platforms and a monstrous new type of people that apparently did not exist in the past.
  11. Megan Redshaw, “Vaccine-Injured Speak Out, Feel Abandoned by Government Who Told Them COVID Shot Was Safe,” Childrens Health Defense Fund, November 3, 2021.
  12. Ed Dowd, “Cause Unknown”: The Epidemic of Sudden Deaths in 2021 & 2022 (Skyhorse, 2022). Website: https://www.theyliedpeopledied.com/: “Between March of 2021 and February of 2022, 61,000 millennials died excessively above the prior 5-year base trend line… The relative timespan and rate of change into the fall of 2021 is a signal that a harmful event occurred to this 25-44 age group. This means that millennials started dying in large numbers at the same times when vaccines and boosters were rolled out. The vaccine clearly had a role, as many previously hesitant folks were forced into compliance.” Or see Aubrey Marcus, “Why Are Healthy People Dying Suddenly Since 2021? w/ Ed Dowd,” January 5, 2023. (31:40~).

Read full story here…

July 3, 2023. READING

There is going to be a big push towards ….  Controlling all of humanity in many inhumane ways, but the tide has turned, and those who are forcing the control are not seeing that.  They live within an environment of their own making, and they bolster one another up with the lie that all is well, but that is not true.

There is also coming on some very intense environmental aspects which will be in the form of weather and earthquakes as well as things coming from the sun.  There will be “accidents’ that will be occurring because the machines that are being used to manipulate weather are based on ancient and outdated models so that when they are turned on, they will not react in the way that they thought.  You see, they have modified things on the Earth in such a way that they no longer work according to the old paradigms.  There will be problems which ultimately refer back to the perpetrators, and you can expect to see a shake up within their ranks, perhaps even some passing on.

As for the outsiders, the ET,s as you call them, they have been waiting and watching, and while the government is attempting to control the whole project of disclosure, they are not in charge of the Outsiders’ actions. There will be a large kerfuffle this month in which some things will be coming forth from unknown sources which can lead to a lot of head scratching as well as head rolling, but those who sought to control disclosure will find out that they re not in charge, and that their powers are limited and being more limited. 

Things are not going to work the way they used, and this is in all areas, the grid, travel, weather, even your CERN is going to find itself somewhat out of control of those scientists who are supposed to be controlling it.  They will not, however be revealing this to the public other than as a leak, and as a result, there will be a shift in the leadership of CERN and some unfortunate “accidents’.

“Who’s Yo’ Daddy?”

Synthetic human embryos created in groundbreaking advance

Exclusive: Breakthrough could aid research into genetic disorders but raises serious ethical and legal issues

Scientists have created synthetic human embryos using stem cells, in a groundbreaking advance that sidesteps the need for eggs or sperm.

Scientists say these model embryos, which resemble those in the earliest stages of human development, could provide a crucial window on the impact of genetic disorders and the biological causes of recurrent miscarriage.

However, the work also raises serious ethical and legal issues as the lab-grown entities fall outside current legislation in the UK and most other countries.

The structures do not have a beating heart or the beginnings of a brain, but include cells that would typically go on to form the placenta, yolk sac and the embryo itself.

Prof Magdalena Żernicka-Goetz, of the University of Cambridge and the California Institute of Technology, described the work in a plenary address on Wednesday at the International Society for Stem Cell Research’s annual meeting in Boston.

“We can create human embryo-like models by the reprogramming of [embryonic stem] cells,” she told the meeting.

There is no near-term prospect of the synthetic embryos being used clinically. It would be illegal to implant them into a patient’s womb, and it is not yet clear whether these structures have the potential to continue maturing beyond the earliest stages of development.

The motivation for the work is for scientists to understand the “black box” period of development that is so called because scientists are only allowed to cultivate embryos in the lab up to a legal limit of 14 days. They then pick up the course of development much further along by looking at pregnancy scans and embryos donated for research.

Robin Lovell-Badge, the head of stem cell biology and developmental genetics at the Francis Crick Institute in London, said: “The idea is that if you really model normal human embryonic development using stem cells, you can gain an awful lot of information about how we begin development, what can go wrong, without having to use early embryos for research.”

Previously, Żernicka-Goetz’s team and a rival group at the Weizmann Institute in Israel showed that stem cells from mice could be encouraged to self-assemble into early embryo-like structures with an intestinal tract, the beginnings of a brain and a beating heart. Since then, a race has been under way to translate this work into human models, and several teams have been able to replicate the very earliest stages of development.

The full details of the latest work, from the Cambridge-Caltech lab, are yet to be published in a journal paper. But, speaking at the conference, Żernicka-Goetz described cultivating the embryos to a stage just beyond the equivalent of 14 days of development for a natural embryo.

The model structures, each grown from a single embryonic stem cell, reached the beginning of a developmental milestone known as gastrulation, when the embryo transforms from being a continuous sheet of cells to forming distinct cell lines and setting up the basic axes of the body. At this stage, the embryo does not yet have a beating heart, gut or beginnings of a brain, but the model showed the presence of primordial cells that are the precursor cells of egg and sperm.

“Our human model is the first three-lineage human embryo model that specifies amnion and germ cells, precursor cells of egg and sperm,” Żernicka-Goetz told the Guardian before the talk. “It’s beautiful and created entirely from embryonic stem cells.”

The development highlights how rapidly the science in this field has outpaced the law, and scientists in the UK and elsewhere are already moving to draw up voluntary guidelines to govern work on synthetic embryos. “If the whole intention is that these models are very much like normal embryos, then in a way they should be treated the same,” Lovell-Badge said. “Currently in legislation they’re not. People are worried about this.”

There is also a significant unanswered question on whether these structures, in theory, have the potential to grow into a living creature. The synthetic embryos grown from mouse cells were reported to appear almost identical to natural embryos. But when they were implanted into the wombs of female mice, they did not develop into live animals. In April, researchers in China created synthetic embryos from monkey cells and implanted them into the wombs of adult monkeys, a few of which showed the initial signs of pregnancy but none of which continued to develop beyond a few days. Scientists say it is not clear whether the barrier to more advanced development is merely technical or has a more fundamental biological cause.

“That’s very difficult to answer. It’s going to be hard to tell whether there’s an intrinsic problem with them or whether it’s just technical,” Lovell-Badge said. This unknown potential made the need for stronger legislation pressing, he said.

from:    https://www.theguardian.com/science/2023/jun/14/synthetic-human-embryos-created-in-groundbreaking-advance

New Info on Just What is in those Jabs

Green Monkey DNA Found in COVID-19 Shots

Analysis by Dr. Joseph MercolaFact Checked
May 31, 2023
Link for Video of Sucharit Bhakdti dscussing this issue:   https://rumble.com/v2owij0-why-the-covid-mrna-vaccines-are-actually-dna-gene-therapies-that-must-be-re.html

STORY AT-A-GLANCE

  • Microbiologist Kevin McKernan — a former researcher and team leader for the MIT Human Genome project — has discovered massive DNA contamination in the mRNA COVID shots, including simian virus 40 (SV40) promoters
  • SV40 has been linked to cancer in humans, including mesotheliomas, lymphomas and cancers of the brain and bone. In 2002, the Lancet published evidence linking polio vaccines contaminated with SV40 to Non-Hodgkin’s lymphoma. According to the authors, the vaccine may be responsible for up to 50% of the 55,000 Non-Hodgkin’s lymphoma cases diagnosed each year
  • The level of contamination varies depending on the platform used to measure it, but no matter which method is used, the level of DNA contamination is significantly higher than the regulatory limits in both Europe and the U.S. The highest level of DNA contamination found was 30%
  • The finding of DNA means the mRNA COVID shots may have the ability to alter the human genome
  • Even if genetic modification does not occur, the fact that you’re getting foreign DNA into your cells poses a risk in and of itself. Partial expression could occur, or it might interfere with other transcription translations that are already in the cell. Cytoplasmic transfection can also allow for genetic manipulation, as the nucleus disassembles and exchanges cellular components with the cytosol during cell division

In the video1 above, Dr. Steven E. Greer interviews microbiologist Kevin McKernan — a former researcher and team leader for the MIT Human Genome project2 — and Dr. Sucharit Bhakdi about the DNA contamination McKernan’s team has found in the Pfizer and Moderna mRNA shots.

As it turns out, spike protein and the mRNA are not the only hazards of these injections. McKernan’s team have also discovered simian virus 40 (SV40) promoters that, for decades, have been suspected of causing cancer in humans, including mesotheliomas, lymphomas and cancers of the brain and bone.3 The findings4,5,6,7 were posted on OSF Preprints in early April 2023. As explained in the abstract:8

“Several methods were deployed to assess the nucleic acid composition of four expired vials of the Moderna and Pfizer bivalent mRNA vaccines. Two vials from each vendor were evaluated … Multiple assays support DNA contamination that exceeds the European Medicines Agency (EMA) 330ng/mg requirement and the FDAs 10ng/dose requirements …”

As noted by Greer,9 this means that governments and drug companies “have misled the world to a far greater extent than previously known.” If these findings are correct, it would also mean that “the so-called ‘vaccines’ are actually altering the human genome and causing permanent production of the deadly spike protein,” and this internal production of spike protein would, in turn, “trigger the immune system to attack its own cells,” Greer says.

In the interview, McKernan explains how the DNA contaminants found in the COVID jabs can result in the genetic modification of the human genome, and Bhakdi reviews how and why the shots can trigger autoimmune diseases.

Background: What Is SV40?

In 2002, the Lancet published10 evidence linking polio vaccines contaminated with SV40 to Non-Hodgkin’s lymphoma. According to the authors, the vaccine may be responsible for up to half the 55,000 Non-Hodgkin’s lymphoma cases diagnosed each year.

How did this simian (monkey) virus get into the human population? According to the late Dr. Maurice Hilleman, a leading vaccine developer, Merck inadvertently unleashed the virus via their polio vaccine.11 It’s unclear exactly when SV40 was eliminated from the polio vaccine. The timing also varies from country to country. For example, SV40-contaminated polio vaccines were administered in Italy as recently as 1999.12

As reported in a Lancet book review of “The Virus and the Vaccine: The True Story of a Cancer-Causing Money Virus, Contaminated Polio Vaccine and the Millions of Americans Exposed”:13

“By 1960, scientists and vaccine manufacturers knew that monkey kidneys were sewers of simian viruses. Such contamination often spoiled cultures, including those of an NIH researcher named Bernice Eddy, who worked on vaccine safety … Her discovery … threatened one of the USA’s most important public-health programs …

Eddy tried to get word out to colleagues but was muzzled and stripped of her vaccine regulatory duties and her laboratory … [Two] Merck researchers, Ben Sweet and Maurice Hilleman, soon identified the rhesus virus later named SV40 — the carcinogenic agent that had eluded Eddy.

In 1963, U.S. authorities decided to switch to African green monkeys, which are not natural hosts of SV40, to produce polio vaccine. In the mid-1970s, after limited epidemiological studies, authorities concluded that although SV40 caused cancer in hamsters, it didn’t seem to do so in people.

Fast forward to the 1990s: Michele Carbone, then at NIH, was working on how SV40 induces cancers in animals. One of these was mesothelioma, a rare cancer of the pleura thought in people to be caused mainly by asbestos. The orthodoxy held that SV40 didn’t cause human cancers.

Emboldened by a 1992 NEJM paper that found DNA ‘footprints’ of SV40 in childhood brain tumors, Carbone tested human mesothelioma tumor biopsies at the National Cancer Institute: 60% contained SV40 DNA. In most, the monkey virus was active and producing proteins.

He published his results in Oncogene in May, 1994, but the NIH declined to publicize them … Carbone … moved to Loyola University. There he discovered how SV40 disables tumor suppressor genes in human mesothelioma, and published his results in Nature Medicine in July, 1997. Studies in Italy, Germany, and the USA also showed associations between SV40 and human cancers.”

mRNA COVID Jabs Contaminated With Double-Stranded DNA

With that background, let’s get back to McKernan’s findings, which in addition to the featured video are also discussed in Daniel Horowitz’s podcast above. In short, his team discovered elevated levels of double-stranded DNA plasmids, including SV40 promoters (DNA sequence that is essential for gene expression) that are known to trigger cancer development when encountering an oncogene (a gene that has the potential to cause cancer).

The level of contamination varies depending on the platform used to measure it, but no matter which method is used, the level of DNA contamination is significantly higher than the regulatory limits in both Europe and the U.S., McKernan says. The highest level of DNA contamination found was 30%, which is rather astounding.

As explained by McKernan, when using a typical PCR test, you’ll be considered positive if the test detects the SARS-CoV-2 virus using a cycle threshold (CT) of about 40. In comparison, the DNA contamination is detected at CTs below 20.

That means the contamination is a million-fold greater than the amount of virus you’d need to have in order to test positive for COVID. “So, there’s an enormous difference here with regards to the amount of material that’s in there,” McKernan says.

In his Substack article,14 he also points out that people who argue that double-stranded DNA and viral RNA is a false equivalency because viral RNA is replication competent, are wrong.

“The majority of the sgRNA you are detecting in a nasal swab in your nose is NOT REPLICATION COMPETENT as shown in Jaafar et al.15 It is just an RNA fragment that should have lower longevity in your cells than dsDNA contaminating fragments,” he writes.

In that Substack article, McKernan has also copied a 2009 study discussing how DNA in vaccines can cause cancer and highlighted the most relevant parts. It’s a helpful resource if you want to learn more.

Quality Control Is Sorely Lacking

As for how SV40 promoters ended up in the mRNA shots, it appears to be related to poor quality control during the manufacturing process, although it’s unclear where in the development SV40 might have sneaked in. Quality control deficiencies may also be responsible for the high rate of anaphylactic reactions we’ve been seeing. McKernan tells Greer:

“It’s in both Moderna and Pfizer. We looked at the bivalent vaccines for both Moderna and Pfizer and only the monovalent vaccines for Pfizer because we didn’t have access to monovalent vaccines for Moderna. In all three cases, the vaccines contain double-stranded DNA contamination.

If you sequence that DNA, you’ll find that it matches what looks to be an expression vector that’s used to make the RNA … Whenever we see DNA contamination, like from plasmids, ending up in any injectable, the first thing people think about is whether there’s any E. coli endotoxin present because that creates anaphylaxis for the injected.

And, of course … there’s a lot of anaphylaxis going on, not only on TV but in the VAERS database. You can see people get injected with this and drop. That could be the background from this E. coli process of manufacturing the DNA …”

Regulatory Agencies Knew There Was a Contamination Problem

In a May 20, 2023, Substack article,16 McKernan points out that Pfizer itself submitted evidence to the European Medicines Agency (EMA) showing sampled lots contained vast differences in the levels of double-stranded DNA contamination.

The arbitrary limit for dsDNA that the EMA came up with was 330 nanograms per milligram (ng/mg). Data submitted to the EMA by Pfizer shows sampled lots had anywhere from 1 ng/mg to 815 ng/mg of DNA. McKernan adds:17

“This limit likely did not consider the potency of this dsDNA contamination if it was packaged in an LNP [lipid nanoparticle]. Packaged dsDNA is more potent as a gene therapy. We now know this DNA is packaged and transfection ready.18 Even lower limits should be applied if the DNA is packaged in transfection ready LNPs …

Even with Pfizer being able to cherry pick the data they provided to the EMA for 10 lots, they see a 1 to 815ng/mg variance. If you were to expand this study to 100 or 1000 lots, you’d likely see another order or two of magnitude variance.”

Double-Stranded DNA May Integrate Into Your Genome

The presence of double-stranded DNA also brings up another major concern, and that is the possibility of genomic integration.

“At least on the Pfizer side of things, it has what’s known as an SV40 promoter. This is an oncogenic virus piece. It’s not the entire virus. However, the small piece is known to drive very aggressive gene expression.

And the concern that people, even at the FDA, have noted in the past whenever injecting double-stranded DNA, is that these things can integrate into the genome,” McKernan says.

While McKernan’s paper does not present evidence of genome integration, it does point out that it’s possible, especially in the presence of SV40 promoters:19

“There has been a healthy debate about the capacity for SARs-CoV-2 to integrate into the human genome … This work has inspired questions regarding the capacity for the mRNA vaccines to also genome integrate. Such an event would require LINE-1 driven reverse transcription of the mRNA into DNA as described by Alden et al.

dsDNA [double-stranded DNA] contamination of sequence encoding the spike protein wouldn’t require LINE-1 for Reverse Transcription and the presence of an SV40 nuclear localization signal in Pfizer’s vaccine vector would further increase the odds of integration.”

Manifold Risks

That said, even if genetic modification does not occur, the fact that you’re getting foreign DNA into your cells poses a risk in and of itself, McKernan says. For example, partial expression could occur, or it might interfere with other transcription translations that are already in the cell.

Bhakdi also points out that the SV40 promoters do not need to be present in the nucleus of the cell for problems to occur. Cytoplasmic transfection can, in and of itself, allow for genetic manipulation, because the nucleus disassembles and exchanges cellular components with the cytosol during cell division.

In addition to having DNA floating around and causing potential problems, the RNA in the COVID jab is also modified to resist breakdown. “So, we have TWO versions of the spike protein floating around that can persist longer than anticipated,” McKernan says, and the spike protein, of course, is the most toxic part of the virus that can cause your body to attack itself.

Both McKernan and Bhakdi are adamant that ALL mRNA “vaccines” must be immediately stopped, whether for human or animal use, due to the magnitude of the risks involved.

‘Alarming Problems’

In the video above,20 Yusuke Murakami, a professor at Tokyo University, expresses alarm over the finding of SV40 promoters in the COVID jabs. The interview is in Japanese but has English subtitles. I’ve included it because I think he does a good job of putting the problem into layman’s terms:

“The Pfizer vaccine has a staggering problem,” Murakami says. “This figure is an enlarged view of Pfizer’s vaccine sequence. As you can see, the Pfizer vaccine sequence contains part of the SV40 sequence here. This sequence is known as a promoter.

Roughly speaking, the promoter causes increased expression of the gene. The problem is that the sequence is present in a well-known carcinogenic virus. The question is why such a sequence that is derived from a cancer virus is present in Pfizer’s vaccine.

There should be absolutely no need for such a carcinogenic virus sequence in the vaccine. This sequence is totally unnecessary for producing the mRNA vaccine. It is a problem that such a sequence is solidly contained in the vaccine.

This is not the only problem. If a sequence like this is present in the DNA, the DNA is easily migrated to the nucleus. So it means that the DNA can easily enter the genome. This is such an alarming problem.

It is essential to remove the sequence. However, Pfizer produced the vaccine without removing the sequence. That is outrageously malicious. This kind of promoter sequence is completely unnecessary for the production of the mRNA vaccine. In fact, SV40 is a promoter of cancer viruses.”

Resources for Those Injured by the COVID Jab

The more we learn about the COVID jabs, the worse they appear. While they suck as vaccines, they’re truly masterful bioweapons, as they’re capable of destroying health in any number of ways, through myriad mechanisms.

If you got one or more jabs and are now reconsidering, first and foremost, never ever take another COVID booster, another mRNA gene therapy shot or regular vaccine. You need to end the assault on your body. Even if you haven’t experienced any obvious side effects, your health may still be impacted long-term, so don’t take any more shots.

If you’re suffering from side effects, your first order of business is to eliminate the spike protein that your body is producing. Two remedies that can do this are hydroxychloroquine and ivermectin. Both of these drugs bind and facilitate the removal of spike protein.

The Front Line COVID-19 Critical Care Alliance (FLCCC) has developed a post-vaccine treatment protocol called I-RECOVER. Since the protocol is continuously updated as more data become available, your best bet is to download the latest version straight from the FLCCC website at covid19criticalcare.com21 (hyperlink to the correct page provided above).

For additional suggestions, check out the World Health Council’s spike protein detox guide,22 which focuses on natural substances like herbs, supplements and teas. To combat neurotoxic effects of spike protein, a March 2022 review paper23 suggests using luteolin and quercetin. Time-restricted eating (TRE) and/or sauna therapy can also help eliminate toxic proteins by stimulating autophagy.

from:    https://articles.mercola.com/sites/articles/archive/2023/05/31/dna-contamination-mrna-covid-shots.aspx?ui=f460707c057231d228aac22d51b97f2a8dcffa7b857ec065e5a5bfbcfab498ac&sd=20211017&cid_source=dnl&cid_medium=email&cid_content=art1ReadMore&cid=20230531&cid=DM1408714&bid=1815660384

“Doctor”(?) Chelsea Clinton Wants Your Kids

‘The Big Catch-Up’: Chelsea Clinton Pushes ‘Largest Childhood Immunization Effort Ever’

Chelsea Clinton aims to provide childhood immunizations to as many children as possible with a new initiative called “The Big Catch-Up” that she touted as “the largest childhood immunization effort ever.” The WHO, UNICEF, GAVI, the Vaccine Alliance and the Bill & Melinda Gates Foundation, along with Immunization Agenda 2030, announced “The Big Catch-Up” last month, which WHO characterized as a “targeted global effort to boost vaccination among children following declines driven by the COVID-19 pandemic.” Clinton complained about the lack of trust in science and public health officials and said that she thinks we need the public sector to stop stripping away  public health emergency powers from state public health agencies.

Chelsea Clinton aims to provide childhood immunizations to as many children as possible with a new initiative called “The Big Catch-Up.”

Speaking at the Brainstorm Health conference hosted by Fortune Magazine last month in Marina del Rey, Calif., the daughter of Bill and Hillary Clinton called the initiative “the largest childhood immunization effort ever.”

“A new effort that we’re a part of is the new initiative launched by the WHO last week to try to catch kids up on their routine immunizations. In 2021 alone more than 25 million kids under the age of 1 missed at least 1 routine immunization and so we’re working with WHO and the Gates Foundation and others to kind of hopefully have the largest childhood immunization effort ever over the next 18 months to catch as many kids up as possible, because no one should die of polio, measles, or pneumonia—including in this country, where we also need people to vaccinate their kids,” she said.

The WHO, UNICEF, GAVI, the Vaccine Alliance and the Bill & Melinda Gates Foundation, along with Immunization Agenda 2030 announced “The Big Catch-Up” last month, which WHO characterized as a “targeted global effort to boost vaccination among children following declines driven by the COVID-19 pandemic.”

“This effort aims to reverse the declines in childhood vaccination recorded in over 100 countries since the pandemic, due to overburdened health services, closed clinics, and disrupted imports and exports of vials, syringes and other medical supplies,” WHO described in a press release.

Read full article here…

from:    https://needtoknow.news/2023/05/the-big-catch-up-chelsea-clinton-pushes-largest-childhood-immunization-effort-ever/