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

Some New “Family Entertainment” from Disney

Disney Produced Cartoon Features Illuminati-Style Elites Drinking Blood and Sacrificing People

A new Disney produced cartoon series is based around a cult of robed elites drinking blood, carrying out rituals including human sacrifice and worshiping an all seeing eye symbol. While some have suggested it is more of the same weird indoctrination programming we’ve come to expect from Disney, the series, aimed at adults, is produced by Mike Judge, the creator of IdiocracyKing of The Hill and Beavis & Butthead, who is known for his anti-establishment contrarian outlook the world we live in and culture.

A new Disney produced cartoon series is based around a cult of robed elites drinking blood, carrying out rituals including human sacrifice and worshipping an all seeing eye symbol.

However, it might not be entirely what you think.

While some have suggested it is more of the same weird indoctrination programming we’ve come to expect from Disney, the series, aimed at adults, is produced by Mike Judge, the creator of Idiocracy, King of The Hill and Beavis & Butthead, who is known for his anti-establishment contrarian outlook on the world we live in.

Here’s the trailer for Praise Petey which is set to premiere on July 21st on Freeform:

Read full article here…

from:    https://needtoknow.news/2023/07/disney-produced-cartoon-features-illuminati-style-elites-drinking-blood-and-sacrificing-people/

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/

Stand up! You Have the Power!

Hey, Check out this video from THE CORBETT REPORT.

There is pushback, and we need to be part of the movement for our own autonomy.

Where we go from here will depend on all of us standing up for our rights as individuals and independent arbiters of our fate;

from:    https://rumble.com/v2zvs94-bohemian-grove-sacrifices-staffers-newworldnextweek.html

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…

“Cultivated” Is Not Necessarily Great

U.S. approves chicken made from cultivated cells, the nation’s first ‘lab-grown’ meat

The Agriculture Department gave the green light to Upside Foods and Good Meat, which had been racing to be the first in the U.S. to sell meat that doesn’t come from slaughtered animals.
Image: Chef Zach Tyndall prepares Good Meat's cultivated chicken at the Eat Just office in Alameda, Calif., on June 14, 2023.

Chef Zach Tyndall prepares Good Meat’s cultivated chicken at the Eat Just office in Alameda, Calif., on June 14. Jeff Chiu / AP

 / Source: Associated Press

For the first time, U.S. regulators on Wednesday approved the sale of chicken made from animal cells, allowing two California companies to offer “lab-grown” meat to the nation’s restaurant tables and eventually, supermarket shelves.

The Agriculture Department gave the green light to Upside Foods and Good Meat, firms that had been racing to be the first in the U.S. to sell meat that doesn’t come from slaughtered animals — what’s now being referred to as “cell-cultivated” or “cultured” meat as it emerges from the laboratory and arrives on dinner plates.

The move launches a new era of meat production aimed at eliminating harm to animals and drastically reducing the environmental impacts of grazing, growing feed for animals and animal waste.

instead of all of that land and all of that water that’s used to feed all of these animals that are slaughtered, we can do it in a different way,” said Josh Tetrick, co-founder and chief executive of Eat Just, which operates Good Meat.

The companies received approvals for federal inspections required to sell meat and poultry in the U.S. The action came months after the U.S. Food and Drug Administration deemed that products from both companies are safe to eat. A manufacturing company called Joinn Biologics, which works with Good Meat, was also cleared to make the products.

Cultivated meat is grown in steel tanks, using cells that come from a living animal, a fertilized egg or a special bank of stored cells. In Upside’s case, it comes out in large sheets that are then formed into shapes like chicken cutlets and sausages. Good Meat, which already sells cultivated meat in Singapore, the first country to allow it, turns masses of chicken cells into cutlets, nuggets, shredded meat and satays.

But don’t look for this novel meat in U.S. grocery stores anytime soon. Cultivated chicken is much more expensive than meat from whole, farmed birds and cannot yet be produced on the scale of traditional meat, said Ricardo San Martin, director of the Alt:Meat Lab at University of California Berkeley.

The companies plan to serve the new food first in exclusive restaurants: Upside has partnered with a San Francisco restaurant called Bar Crenn, while Good Meat dishes will be served at a Washington, D.C., restaurant run by chef and owner Jose Andrés.

Company officials are quick to note the products are meat, not substitutes like the Impossible Burger or offerings from Beyond Meat, which are made from plant proteins and other ingredients.

Globally, more than 150 companies are focusing on meat from cells, not only chicken but pork, lamb, fish and beef, which scientists say has the biggest impact on the environment.

Upside, based in Berkeley, operates a 70,000-square-foot building in nearby Emeryville. On a recent Tuesday, visitors entered a gleaming commercial kitchen where chef Jess Weaver was sauteeing a cultivated chicken filet in a white wine butter sauce with tomatoes, capers and green onions.

The finished chicken breast product was slightly paler than the grocery store version. Otherwise it looked, cooked, smelled and tasted like any other pan-fried poultry.

“The most common response we get is, ‘Oh, it tastes like chicken,’” said Amy Chen, Upside’s chief operating officer.

Good Meat, based in Alameda, operates a 100,000-square-foot plant, where chef Zach Tyndall dished up a smoked chicken salad on a sunny June afternoon. He followed it with a chicken “thigh” served on a bed of potato puree with a mushroom-vegetable demi-glace and tiny purple cauliflower florets. The Good Meat chicken product will come pre-cooked, requiring only heating to use in a range of dishes.

Chen acknowledged that many consumers are skeptical, even squeamish, about the thought of eating chicken grown from cells.

“We call it the ‘ick factor,’” she said.

Image: A scientist works in a cellular agriculture lab at Eat Just in Alameda, Calif., on June 14, 2023.
A scientist works in a cellular agriculture lab at Eat Just in Alameda, Calif., on June 14. Jeff Chiu / AP

The sentiment was echoed in a recent poll conducted by The Associated Press-NORC Center for Public Affairs Research. Half of U.S. adults said that they are unlikely to try meat grown using cells from animals. When asked to choose from a list of reasons for their reluctance, most who said they’d be unlikely to try it said “it just sounds weird.” About half said they don’t think it would be safe.

But once people understand how the meat is made, they’re more accepting, Chen said. And once they taste it, they’re usually sold.

“It is the meat that you’ve always known and loved,” she said.

Cultivated meat begins with cells. Upside experts take cells from live animals, choosing those most likely to taste good and to reproduce quickly and consistently, forming high-quality meat, Chen said. Good Meat products are created from a master cell bank formed from a commercially available chicken cell line.

Once the cell lines are selected, they’re combined with a broth-like mixture that includes the amino acids, fatty acids, sugars, salts, vitamins and other elements cells need to grow. Inside the tanks, called cultivators, the cells grow, proliferating quickly. At Upside, muscle and connective tissue cells grow together, forming large sheets. After about three weeks, the sheets of poultry cells are removed from the tanks and formed into cutlets, sausages or other foods. Good Meat cells grow into large masses, which are shaped into a range of meat products.

Both firms emphasized that initial production will be limited. The Emeryville facility can produce up to 50,000 pounds of cultivated meat products a year, though the goal is to expand to 400,000 pounds per year, Upside officials said. Good Meat officials wouldn’t estimate a production goal.

By comparison, the U.S. produces about 50 billion pounds of chicken per year.

It could take a few years before consumers see the products in more restaurants and seven to 10 years before they hit the wider market, said Sebastian Bohn, who specializes in cell-based foods at CRB, a Missouri firm that designs and builds facilities for pharmaceutical, biotech and food companies.

Cost will be another sticking point. Neither Upside nor Good Meat officials would reveal the price of a single chicken cutlet, saying only that it’s been reduced by orders of magnitude since the firms began offering demonstrations. Eventually, the price is expected to mirror high-end organic chicken, which sells for up to $20 per pound.

San Martin said he’s concerned that cultivated meat may wind up being an alternative to traditional meat for rich people, but will do little for the environment if it remains a niche product.

“If some high-end or affluent people want to eat this instead of a chicken, it’s good,” he said. “Will that mean you will feed chicken to poor people? I honestly don’t see it.”

Tetrick said he shares critics’ concerns about the challenges of producing an affordable, novel meat product for the world. But he emphasized that traditional meat production is so damaging to the planet it requires an alternative — preferably one that doesn’t require giving up meat all together.

“I miss meat,” said Tetrick, who grew up in Alabama eating chicken wings and barbecue. “There should be a different way that people can enjoy chicken and beef and pork with their families.”

No, Dear, There is a First Amendment RIght

Court Hands Down A MASSIVE Victory for Freedom on the Fourth of July

Court Hands Down A MASSIVE Victory for Freedom on the Fourth of July
(AP Photo/Andrew Harnik)
On Independence Day, July 4, 2023, the forces of freedom won a major victory, and the Biden regime suffered a historic defeat. May there be many more days like this.

The Biden regime is authoritarian to the core. Like every hard-Left authority in the history of the world, it is intolerant of dissent and determined to stamp out all opposition, not by defeating it at the ballot box, and certainly not by besting it in the court of public opinion, but by forcibly silencing it. But on Tuesday, Judge Terry Doughty, Chief U.S. district judge of the United States District Court for the Western District of Louisiana, put a massive roadblock in the way of Biden’s handlers’ ongoing efforts to ensure that only their own perspective can be heard in the American public square.

In a landmark ruling in Missouri v. Biden, Doughty struck back hard against what he called “the most massive attack against free speech in United States’ history.” Doughty even began his decision by quoting the most famous adage regarding the importance of the freedom of speech: “I may disapprove of what you say, but I would defend to the death your right to say it,” a statement that is often attributed to Voltaire but which Doughty credits to the early twentieth-century English writer Evelyn Beatrice Hall (whom he mistakenly calls Hill, but that doesn’t detract from the power of his ruling).

Doughty declares that “in their attempts to suppress alleged disinformation, the Federal Government, and particularly the Defendants named here, are alleged to have blatantly ignored the First Amendment’s right to free speech.” He noted that “Plaintiffs allege that Defendants, through public pressure campaigns, private meetings, and other forms of direct communication, regarding what Defendants described as ‘disinformation,’ ‘misinformation,’ and ‘malinformation,’ have colluded with and/or coerced social-media platforms to suppress disfavored speakers, viewpoints, and content on social-media platforms.”

Specifically, Doughty noted:

Plaintiffs allege that Defendants suppressed conservative-leaning free speech, such as: (1) suppressing the Hunter Biden laptop story prior to the 2020 Presidential election; (2) suppressing speech about the lab-leak theory of COVID-19’s origin; (3) suppressing speech about the efficiency of masks and COVID-19 lockdowns; (4) suppressing speech about the efficiency of COVID-19 vaccines; (5) suppressing speech about election integrity in the 2020 presidential election; (6) suppressing speech about the security of voting by mail; (7) suppressing parody content about Defendants; (8) suppressing negative posts about the economy; and (9) suppressing negative posts about President Biden.

All that is abundantly true, and there are plenty of other examples of the regime’s hatred of dissent as well. Regime spokesbeings, however, will tell you that all they really want to do is protect poor, ignorant, distracted, gullible Americans from “disinformation.” It became clear when the Biden regime established its ill-fated and quickly disbanded Disinformation Governance Board that it had decided that labeling reports that departed from the officially approved line as “disinformation” was a likely winning strategy, both to circumvent the First Amendment and to hoodwink Americans into thinking that the crushing of dissent was a valuable service.

Related: Stanford University Launches New Censorship Initiative to Save ‘Our Democracy’ by Destroying It

Doughty, however, pointed out that it was not the government’s role at all to silence opposition voices; rather, he reminds us that “the principal function of free speech under the United States’ system of government is to invite dispute; it may indeed best serve its high purpose when it induces a condition of unrest, creates dissatisfaction with conditions as they are, or even stirs people to anger.” This is as far from the Biden regime’s conception of the function of free speech as Los Angeles is from Pluto’s moons, and that’s precisely why this ruling is so urgently needed, and so welcome.

Doughty wrote: “During the COVID-19 pandemic, a period perhaps best characterized by widespread doubt and uncertainty, the United States Government seems to have assumed a role similar to an Orwellian ‘Ministry of Truth.’ The Plaintiffs have presented substantial evidence in support of their claims that they were the victims of a far-reaching and widespread censorship campaign.” He added: “It is quite telling that each example or category of suppressed speech was conservative in nature. This targeted suppression of conservative ideas is a perfect example of viewpoint discrimination of political speech. American citizens have the right to engage in free debate about the significant issues affecting the country.” Yes, they do, and in Missouri v. Biden, Doughty has done a great deal to protect that right. This decision prohibits the government from working with social media giants to censor American citizens.

Will the regime fight back? Almost certainly. Will it craft a deceptive, Orwellian, disingenuous, paternalistic argument for censorship based on its claimed responsibility to protect Americans from “disinformation”? That seems likely as well. But the more it fights in cases of this kind, the more its authoritarian nature becomes clear. Will Americans quietly accept the yoke of censorship? We have a history of resisting tyranny. It is no accident, comrade, as Biden’s Marxist friends would say, that Doughty’s ruling came on Independence Day.

from:    https://pjmedia.com/news-and-politics/robert-spencer/2023/07/04/court-hands-down-a-massive-victory-for-freedom-on-the-fourth-of-july-n1708218

A Movie That Brings Attention to the Horror of Human Trafficking

Sound of Freedom Hero: ‘Media Running Interference For Pedophiles And Human Traffickers Is Sick’

Sound of Freedom is a movie based on a true story about former Homeland Security agent Tim Ballard and his fight against child trafficking and pedophilia. The Washington Post, Rolling Stone, Media Matters, Jezebel, the Guardian, and other leftist media outlets, published articles trying to conflate child abuse with QAnon conspiracy theories to discredit the facts about child trafficking and mass immigration.

The real life former government agent who exposed child trafficking rings, inspiring the wildly popular new film ‘Sound of Freedom’, has hit back at a coordinated media effort to categorise the movie as some sort of conspiracy theorist’s wet dream.

In a Fox News interview, Tim Ballard, played by Jim Caviezel in the movie, responded to bizarre efforts to label it a ‘QAnon’ production.

“I can’t explain, and neither can they,” Ballard urged, adding “Every show I’ve seen, they just like to throw the word out, ‘QAnon.’ They make zero connection to the actual story. It’s very difficult to make that connection when it’s actually based on a true story.”

“Where is the QAnon doctrine being spewed in the film and the script?” Ballard demanded to know, adding “This is just some other agenda.”

“Who would want to get the backs or run interference for pedophiles and human traffickers?” Ballard emphasised, adding “That’s the more important question in all this. Why would you want to lie to push an agenda whose goal is to have children be in captivity? It’s kind of sick.”

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Read full article here…

(Note:  Lots of opinions and reviews on the movie in the full article:  https://summit.news/2023/07/11/real-life-sound-of-freedom-hero-media-running-interference-for-pedophiles-and-human-traffickers-is-sick/ )

from:    https://needtoknow.news/2023/07/sound-of-freedom-hero-media-running-interference-for-pedophiles-and-human-traffickers-is-sick/

Taking on Gang Violence in El Salvador

El Salvador President Bukele’s Wildly Popular Gang Crackdown is Reducing Illegal Immigration to US

The Wall Street Journal reported that El Salvador President Nayib Bukele’s successful crackdown on MS-13 gang members has led to a dramatic 44% reduction in the number of Salvadorans illegally crossing the southern border into the US. El Salvador, was once known for having the world’s highest murder rate, now has the world’s highest incarceration rate, 68,000 prisoners, which is about 1% of their population. The strategy has helped lower homicides by 92% compared with 2015, giving Bukele the support of nine of every 10 Salvadorans. Ecuador, Guatemala and Colombia are considering copying Bukele’s policies.The success of Bukele’s heavy-handed crackdown has made fools of our ruling elites who insist restorative justice and throwing open our nation’s prisons is how you create peace.

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President Nayib Bukele’s successful crackdown on MS-13 gang members has led to a dramatic reduction in the number of Salvadorans illegally crossing our southern border, the Wall Street Journal reports.

From The Wall Street Journal, “The Country With the Highest Murder Rate Now Has the Highest Incarceration Rate”:

El Salvador, long whipsawed by gang violence that made it one of the world’s most dangerous countries, turned things around by jailing huge swaths of its population. The country once known for having the world’s highest murder rate now has the world’s highest incarceration rate—about double that of the U.S.

Since March 2022, President Nayib Bukele’s government has implemented a campaign to arrest en masse suspected members of the MS-13 and 18th Street gangs that have long terrorized the impoverished Central American nation, blocking economic growth and stoking U.S.-bound migration.

The strategy has helped lower homicides by 92% compared with 2015, giving Bukele the support of nine of every 10 Salvadorans, polls show. The number of Salvadorans illegally crossing the U.S.-Mexico border has dropped by 44%.

These numbers are even more significant considering illegal immigration overall has hit record levels thanks to the Biden regime’s open borders policies.

It also has put some 68,000 people in this Massachusetts-size country of 6.3 million behind bars. That’s more than 1% of the population, according to World Prison Brief, an online database on correctional systems. Rights groups said the campaign has swept up innocent people, especially among the country’s poor and indigenous communities, who are held for long periods in harsh conditions without trial.

Responding to allegations of prisoner mistreatment, Bukele during a cabinet meeting in October said, “Yes, they’ll have human rights. But the human rights of honest people are more important.”

[…] Detentions of Salvadorans, once one of the largest groups trying to cross the southwestern border, illegally crossing have dropped to about 36,500 in the eight months through May of this fiscal year from more than 65,000 in the same period a year earlier, just before the campaign began. 

It was reported in 2010 that around one fifth the entire population of El Salvador was living in the US.

MS-13 gang members make headlines every week for committing heinous murders in cities throughout the US.

We’re supposed to believe these gang members have a “spark of divinity” inside them and the diversity they bring is “our greatest strength.”

The success of Bukele’s heavy-handed crackdown has made fools of our ruling elites who insist “restorative justice” and throwing open our nation’s prisons is how you create peace.

 

According to the WSJ, other Latin American countries “grappl[ing] with their own high murder rates” are considering following in Bukele’s footsteps:

Ecuadoreans, one of the largest nationalities heading to the U.S., have seen the homicide rate in their country quadruple from 2019 through 2022. Some politicians, such as Cynthia Viteria, who until May served as mayor of the violent Ecuadorean city of Guayaquil, encouraged Ecuador’s government to mimic the Salvadoran leader’s policies to bring down crime and stop the killing of police officers.

“It’s simple, just copy him. Do what Bukele’s doing,” she said in September. “The solutions are out there, for those who have the guts to implement them.”

Jan Topic, an independent presidential candidate in Ecuador and a Bukele admirer, said his experience as a French foreign legion sniper serving in Syria and Ukraine would help him bring order to the streets and gang-controlled prisons.

In Guatemala, several presidential candidates adopted a security agenda inspired on Bukele’s policies in this summer’s election.

In Colombia, beset by armed groups in much of the countryside, the opposition Democratic Center party recently invited Bukele to visit the country and showered him with praise after leftist president, Gustavo Petro, compared El Salvador’s overcrowded jails to concentration camps.

“I think I’ll go on vacation to Colombia,” Bukele quipped on Twitter.

The scale of MS-13’s extortion was tremendous:

Former central bank governor Carlos Acevedo said that gangs raked in an estimated $500 million a year from extortion paid by businesses and residents. Multilateral organizations estimated that crime cost El Salvador 15% of its $29 billion economy.

Those losses are now being reversed, business groups said. In a survey earlier this year by the National Association of Private Enterprise, the country’s largest business group, members reported drops of 40% to 70% in extortion since mid-2022.

[…] more than 60% of Salvadorans said they didn’t care if their government was democratic as long as it solved their day-to-day problems, according to a survey by Chile-based regional pollster Latinobarometro in 2021. 

[…] Public-bus operators were robbed of at least $20 million a year through extortion, according to Genaro Ramírez, president of El Salvador’s public transport bus association. Extortion had become so institutionalized that Ramirez said a bank asked him for detailed information on payments to gangs when he once applied for a business loan. Gangs also boarded buses to rob passengers. 

Some 3,000 public transport workers and bus owners were killed in gang crossfire and attacks over the past two decades, Ramírez said. In 2010, after a bus owner refused to pay extortion, at least 17 people were killed when gangsters doused a bus full of passengers with gasoline and set it ablaze, then fired bullets at anyone who tried to run out. The incident transfixed Salvadorans.

Over the past year, extortion has fallen to “negligible sums,” Ramírez said. He credited the anti-gang campaign, calling it harsh but necessary.

“Of course, there is going to be collateral damage, nothing is perfect,” said Ramírez. “But I can’t criticize what’s working.”

The Biden regime has had nothing but criticism for Bukele for undermining what they call “democracy.”

Read full article here

from:    https://needtoknow.news/2023/07/el-salvador-president-bukeles-wildly-popular-gang-crackdown-is-reducing-illegal-immigration-to-us/