by JD Rucker NOQ Report Joe Rogan, Kirstie Alley, and a handful of other celebrities have brought out the anti-Ivermectin wolves in America. Mainstream media is in full attack-mode. Big Tech is censoring posts to the point that people are coming up with creative ways to indicate they’re even talking about Ivermectin so as not […]
Shocking Conclusions from Africa Study Expose Why Big Pharma’s Puppets are Suppressing Ivermectin Data — The Most Revolutionary Act
| I received an email from USDA about commenting on Meat and Poultry Products Derived from Animal Cells? USDA Seeks Comments on the Labeling of Meat and Poultry Products Derived from Animal Cells The U.S. Department of Agriculture’s (USDA) Food Safety and Inspection Service (FSIS) published today an advance notice of proposed rulemaking (ANPR) to solicit comments and information regarding the labeling of meat and poultry products made using cultured cells derived from animals under FSIS jurisdiction. FSIS will use these comments to inform future regulatory requirements for the labeling of such food products. |
After receiving the above email from USDA, I decided that I needed to know what the hell they were talking about. WTF is “Meat and Poultry Products Derived from Animal Cells? Sound totally sickening. Like gag a maggot!
Well it is:
From: https://extension.psu.edu/cell-culture-technology-and-potential-impacts-on-livestock-production
Cell-culture Technology and Potential Impacts on Livestock Production
Cell-culture based production of meat is expanding in the food industry. Understand the potential impacts to your herd to prepare for this new frontier in meat production.
Updated: October 5, 2018
PLEASE NOTE THAT I DELETED THE PICTURE USED IN THE ARTICLE, SO AS NOT TO BE VIOLATING COPYRIGHTS OF ANYONE, AND INSERTED A PICTURE FROM AN INTERNET SOURCE THAT ALLOWS USE OF PICTURES.
Cellular agriculture has quickly metamorphized from an internet curiosity to a serious policy issue, and producers and consumers alike are looking for greater clarity about what this new technology might mean for their business, as well as their dinner table.
The introduction of cell-culture based food products is likely to bring substantial changes to meat processing and the livestock production agriculture sector. Recently, U.S. Food and Drug Administration and the U.S. Department of Agriculture have joined forces to share oversight of the cellular based meat industry. These two federal agencies together will regulate cell cultured food products derived from livestock and poultry tissue based on the respective regulatory expertise of the organizations. A joint statement released last month by the two agencies said they would be working together to “foster these innovative food products and maintain the highest standards of public health.” The FDA will be in charge of regulating the collection, banking and growing of the cells used to make artificial meat, while the USDA will work on the production and labeling of food products.
Due to the increasing complexity of modern food production and governance, the conversation around cell-cultured food technology might be confusing. This article will provide you with useful background information on the scientific history and current state of cell-culture technology in food production. In addition, an overview of the implications of this technology on meat product labeling, meat production, and livestock agriculture will be provided.
Current State of Cell-culture Meat Production
The application of cell-culture based food production is possible through utilizing bioengineering processes that have already been well established in both food and pharmaceuticals. Application of cell-culture technology into meat production shares similar objectives with the modern livestock and meat production industries: maximize production and minimize inputs. In traditional livestock production, improvements to efficiency of tissue production has been accomplished through selective breeding, specialized nutrition programs, improved housing facilities, and advanced veterinary care Cell-cultured meat production seeks to further improve efficiency by optimizing the energy and resource expenditures devoted to building fat and muscle, while eliminating the need to fuel growth of other animal tissues that are considered low value food products in the current American marketplace.
The field of cell-cultured tissue production has been well established in the bioengineering and pharmaceutical production. The application of this technology to meat production, however, has emerged only recently. Pioneering efforts in cell-cultured meat production were inspired two Australian bioengineers who showcased this possibility at an art exhibit in the early 2000s. Specifically, production of cell-cultured meat featured in the art exhibit involved the construction of muscle utilizing embryonic stem cells, on specialty scaffolding, and application of appropriate nutrition and stimulation were able to form muscle fibers that make up the meat product. This conceptual demonstration inspired others to consider the possibility of scaling their technique to an industrial level. Small working groups of tissue engineers and meat scientists continued to advance the field from the mid-2000s to the mid-2010s, either through spin-offs projects on medical research grants or through direct funding from private investors and government research agencies. In 2009, it was reported that the first in vitro pork fillet was produced at Eindhoven University in Holland; however, the fillet was not considered to be fit for human consumption. In 2013, a momentous breakthrough occurred when the first ever cell culture-based beef burger was presented to a celebrity chef at a widely publicized taste test. This event drew journalists, scientists, meat processors, and venture capitalists from around the globe, and their contributions ultimately generated hundreds of millions of dollars that have been invested in cell-culture based agriculture in recent years. To date, while there are now several dozens of cell-culture based meat production companies, including JUST, Memphis Meats, and Mosa Meats, these companies have yet to roll out a product that is ready for public distribution.
The Issue with Labeling and Regulation
Even though cell-culture based meat products are not yet ready for market, the issue of what to call them has already arisen. Standards of identity and labeling for foods have been a controversial topic for as long as agricultural societies have been marketing food to consumers. A familiar example of this controversy is the presence of numerous dairy and dairy-type products seen in the market place. In addition to ‘milk’ produced by livestock, alternative ‘milk’ products are found from soy, almond, and other alternatives that provide the consumer with numerous choices of nutrient-dense liquids to offer their families. The meat industry is not exempt from this food labeling and marketing paradox. For example, ground beef ‘burger’ patties versus plant-based ‘burger’ patties compete for market share and provide consumers with nutritious choices of similar form. However, the labeling controversy contributes to persistent confusion about nutritional value, production methods, and safety of food products among consumers.
Confusion surrounding nutritional value of food products and food production methods are likely at the forefront of the labeling argument for most producers, particularly given evidence that 64% of consumers do not recognize animal meats as a high-quality source of protein. Producers are also aware that labeling concerns extend to production techniques surrounding food products and consumer goods. Meat production methods, regardless of origin from livestock or cell-culture, are likely to be scrutinized by American consumers; many Americans still hold negative attitudes toward certain technology in food production, with genetically modified foods as the primary example of this aversion. This perception can play a critical role in how newly developed products may be perceived when placed next to traditional food products, particularly from animal sources. This emphasizes the point that labeling is a concern for all involved in meat production, not just livestock producers.
Food product labeling is currently regulated as it pertains to certain methods of production (Certified Organic) or food safety. The current debate about labeling for cell-culture meat products is directly related to food safety. To reference our previous ‘burger’ example, in the ‘burger’ industry, USDA-FSIS enforces the labeling and safety requirements for animal sources of protein, whereas plant sources of protein are regulated by FDA. This dynamic may change when the two ‘burger’ choices exist from the same (animal) protein source. Several names and labels have recently surfaced in the media to describe cell-culture based protein foods that originate from animal muscle cells. Some of the popular nomenclature includes the following: “in vitro” meat, “lab-grown” meat, “cultured” meat, “test-tube” meat, “fake” meat, “clean” meat, and most recently, “cell-based” meat. Labeling a food product as “meat” may also influence the regulatory body that oversees production. Remember, products that are currently labeled as “meat”, that are produced and sold in the United States, are regulated by USDA-FSIS. Some have proposed that “clean” or “cultured” meat products, although labeled as “meat” by companies producing cell-cultured food products, be regulated by the FDA, which traditionally oversees plant-based food items. So how will the new meat product be labeled? And, who should regulate cell cultured meat products? These are important questions to consider when discussing the future of food products that originate from alternative proteins and cell-cultured meat products alike as they progress toward becoming a reality in your local markets.
Actions Taken
Regardless of an individual’s personal views on alternative protein foods, this new technology is progressing rapidly, and it may compete for future market share in the meat sector. In an attempt to clarify the “meat” labeling question, the state of Missouri (MO) recently took a step to clearly define that “meat” sold in the state of MO had to come from “livestock or poultry carcass[es] or part[s] thereof” (Senate Bill 627 & 925). This legislation agrees with perspectives shared by the National Cattlemen’s Beef Association (NCBA) and the Missouri Cattlemen’s Association. While this bit of legislation in Missouri was sparked by plant-based products being labeled as “meat”, the argument on a national level remains to be determined. What will be in a package of beef in the future? Groups opposed to this type of legislation argue that this law is unconstitutional and violates first amendment rights. However, according to the United States government (21 U.S. Code § 601(j)), meat “is made wholly or in part from any meat or other portion of the carcass of any cattle, sheep, swine, or goats”. It is this term ‘in part’ that plays a significant role in interpretation of the law, hence the labeling dilemma.
Concerns about regulation and labeling have been emphasized by numerous livestock organizations, not just the NCBA. These organization include: National Pork Producers Council (NPPC), National Chicken Council (NCC), National Turkey Federation (NTF), American Sheep Industry Association (ASIA), and the American Farm Bureau Federation (AFBF). In response to a meeting hosted by the FDA on July 12th of 2018, this group of concerned meat and livestock organizations directly addressed the current regulation quandary in a group letter to President Trump on July 26, 2018. This letter indicates the signatories’ support for the USDA to regulate cell-culture based meat products. The group supports current role of USDA in regulation and preservation of fair competition in the meat market place. Through the current role of the USDA in facilitating daily inspection and food safety among current meat production, this group suggests that consistency of this role across all meat products will prevent confusion among consumers from misleading regulations and labeling. In contrast, the U.S. Cattlemen’s Association (USCA) is currently pushing for separate labels altogether to be used on cell-cultured versus farm-raised meat products. The USCA argues that the labeling of cell-cultured products as “beef” detracts from the brand that cattle producers have worked hard to acquire and uphold for their product. Similarly, cell-cultured meat production stakeholders, including Memphis Meats, sent a joint letter to the White House on August 23rd requesting that cell-cultured food products be regulated by FDA during the product development phase, however, it was also requested in their letter to transition monitoring responsibility to the USDA to ensure post-market safety and labeling compliance. Leaders representing the North American Meat Institute supported letters submitted to the current administration from both the livestock and cell-cultured meat production focused groups. The regulatory debate surrounding cell-cultured meat products is quite dynamic; stakeholder alliances that are evolving may indicate that this debate is far from being settled.
Currently, regulation of safe food production is handled between FDA and USDA-FSIS. FDA inspected food is governed by the Food Safety Modernization Act (FSMA) whereas USDA-FSIS establishments comply with the Pathogen Reduction Act and HACCP-based inspection. Although complying with these regulatory acts have similar goals in safety, some of the regulatory statutes differ in design and methods of regulatory compliance. Companies producing cell culture-based meat products argue that the food is produced in a sterile environment, and therefore, should not be subjected to USDA-FSIS oversight, hence the verbiage “clean” meat. It should be similarly noted that meat from healthy livestock is also produced in a ‘sterile’ environment. The act of cutting into the carcass, and thus exposing tissue to outside contaminants, is what initiates the risk of food-borne pathogen contamination. Regardless of the environment where cell-cultured meat is manufactured, the product that is being consumed will eventually be exposed to the same packaging materials and storage conditions as traditional wholesale and retail “meat” products. This inevitable exposure would place cell-cultured meat products at similar risks of contamination as meat derived from whole tissue cuts of livestock. Food safety concerns should remain at the top of the list when considering how to handle regulations among all methods of meat production.
Are Livestock in Limbo?
Major meat packers, including Tyson and Cargill, are recognizing the potential market impacts of alternative protein sources through proactive investment in cell-cultured meat companies and technologies. Partnerships with meat packers may expand in cell-cultured meat production, as JUST (a start-up company specializing in plant-based protein and cellular agriculture) plans to issue commercial product licenses to traditional meat processing companies in exchange for royalties and prepayments. Livestock producers, on the other hand, have a distinct, yet potentially overlapping, set of interests with respect to cell-culture meat production technology.
Relationships of livestock producers to meat packers currently takes on a variety of forms. In the poultry industry, many of the birds raised for meat production are owned by the meat packer, such as Tyson or Perdue. This ownership of animals and meat is referred to as vertically integrated. In the pork industry, vertical integration occurs in full ownership or through contracted relationships with meat packers. These integrated relationships may benefit from the support of their integrators, like Tyson, should the packer choose to differentiate between the meat products they offer. However, they may also face further competition within their own supplier system. For pork, this means that the demands for further processed meats, such as sausages and deli products, may be met more so through the utilization of cell-cultured meat products, as sales of whole pork cuts continue to struggle, outside of bacon. The beef industry is largely segmented, in contrast, and traditionally does not utilize an integrated relationship model with packers. This leaves beef cattle producers without an established relationship with a packer are much more vulnerable to market fluctuations and additional competition from products bearing a brand they have worked hard to promote as a quality product (i.e. “beef”). This may be why the NCBA and USCA have been very vocal in the labeling debate, as discussed earlier, in order to protect the associations with a name they have created. This vulnerability to market trends and fluctuations would be similar for less popular meat products, such as sheep, goat, and other exotic meat choices. Regardless, the relationship between meat packers and cell-culture meat product start-up companies will directly affect integrated and partially integrated producers. Conversations among the packers and the poultry and swine producers are necessary to understand the impacts of this investment interest in cell culture-based meat production.
Interest in strategic engagement with the burgeoning cell-culture meat industry is growing among livestock producers. Indeed, new livestock markets may be created in conjunction with cell culture-based meat production. For example, cellular agriculture depends on cell lines from healthy animals. This dependence will continue to mean a reliance on livestock production, but with an emphasis on fewer animals meeting specific needs. Livestock producers who provide cell lines for cellular agriculture companies may therefore open new windows of opportunity for entrepreneurial producers, focusing on the diversity and specialty (genetics, welfare, health, nutrition) of their livestock products over quantity. In such a system, Kobe beef may transition from being a luxury to one of the most widely consumed meat products. Traditional livestock producers may also find economic opportunities in this expanding industry by leveraging their unique knowledge and expertise in product development, consultation, biosecurity, logistics, supply chains, agribusiness management, and sales. Animal feed growers and processors, on the other hand, may find opportunities in providing feedstock for cell culture growth mediums.
The future of cell-cultured meat and food production could signify dramatic changes to global agricultural markets, however, livestock producers have long weathered risk, uncertainty, and fluctuation in the market by embracing change, innovation, and strategic adaptation. To quote Bill Northey, USDA Under Secretary for Farm and Foreign Agricultural Services, “Farmers are problem solvers, they think outside [of] the box.” To be sure, many questions about the meaning and potential of cellular agriculture for traditional agriculture producers and consumers have yet to be answered. Participation in the conversations being held now, and likely those in the future, will be an important step for producers and consumers to make their voices heard as this discussion moves forward. Penn State Extension is continuing to monitor this evolving industry and stands ready to provide science-based consultation, support, and partnership for all stakeholders.
Bottom of Form
https://onemoresoul.com/news-commentary/products-that-use-aborted-fetuses.html
Do some products contain fetal parts? The short gruesome answer: Yes.
Today’s consumer products are not the soap and lampshades of recycled Nazi concentration camp victims. The new utilitarian use of people is a sophisticated enterprise, not visible to the human eye.
Perhaps you are a diligent supporter and promoter of pro-life legislation, only vote for pro-life candidates, avoid entertainment from musicians and actors who openly support Planned Parenthood. Regardless, you may unwittingly be cooperating in aborted fetal cell research by purchasing products that use aborted fetuses, either in the product itself or in its development.
One might take Enbrel (Amgen) to relieve Rheumatoid Arthritis. Your husband was given Zoastavax (Merck), a Shingles vaccine, at his annual physical. Your mother with diabetes and renal failure is prescribed Arensep (Amgen). Your grandfather is given the blood product Repro (Eli Lilly) during an angioplasty. The local school district requires that your grandchildren receive the MMRII (the Merck Measles-Mumps-Rubella vaccine). Your daughter and son use coffee creamers and eat soup with artificial flavor enhancers (Senomyx/Firmenich) tested on artificial taste buds engineered from aborted fetal cells.
Because of the vagary of FDA labeling, unless you are proficient at reading patents and pharmaceutical inserts you wouldn’t know aborted fetal parts were there without someone to tell you.
Luckily, that someone is the watchdog group Children of God for Life (COG), a pro-life public citizen group which tracks the use of aborted fetal parts. Under the leadership of Executive Director Debi Vinnedge, COG publishes a downloadable list of products that use aborted fetuses currently available in the U.S.
Products related to fetal material can be broken down into roughly 3 categories: artificial flavors, cosmetics, and medicines/vaccines.
To be clear, food and beverages do not contain any aborted fetal material; however, they may be tastier because of it. How is that?
The American biotech company Senomyx has developed chemical additives that can enhance flavor and smell. To do this, they had to produce an army of never-tiring taste testers–that is, flavor receptors engineered from human embryonic kidney cells (HEK 293, fetal cell line popular in pharmaceutical research).[1] These artificial taste buds can tell product developers which products the public will crave. The goal is to do a taste bud “sleight of hand,” creating low-sugar and low-sodium products that taste sweet or salty while actually using less sugar or sodium in the product.
Does your Nestle Coffee-mate Pumpkin Spice refrigerated creamer taste more like autumn? Does your Maggi bouillon taste just like chicken? Thank Senomyx.
The laboratory-created artificial enhancers do not have to be tested at length by the FDA because the Senomyx chemical “flavor compounds are used in proportions less than one part per million” and can be classified as artificial flavors.[2]
In 2005, Senomyx had contracts to develop products for Kraft Foods, Nestle, Campbell Soup and Coca-Cola.[3] However, when it was discovered in 2011 that PepsiCo was using Senomyx to develop a reduced sugar beverage, a boycott ensued that caused Kraft-Cadbury Adams LLC and Campbell Soup cancelled their contracts with Senomyx. In a 2012 letter to Children of God for Life, PepsiCo stated, “Senomyx does not use HEK cells or any other tissues or cell lines derived from human embryos or fetuses for research performed on behalf of PepsiCo.”[4] To that effect, PepsiCo is working with Senomyx on two products developed with Sweetmyx 617, a new Senomyx sweet taste modifier.[5]
In November 2018, the Swiss company Firmenich acquired Senomyx, Inc. Firmenich describes itself as “a global leader in taste innovation and expert in sweet, cooling and bitter solutions.”
The fountain of youth…is babies.
Commercially, it’s known as Processed Skin Proteins (PSP), developed at the University of Lausanne to heal burns and wounds by regenerating traumatized skin. The fetal skin cell line was taken from an electively aborted baby whose body was donated to the University.[6]
Neocutis, a San Francisco-based firm, uses PSP in some of their anti-aging skin products. Their website claims the trademarked PSP “harnesses the power of Human Growth Factors, Interleukins and other Cytokines, to help deliver state-of-the-art skin revitalization.”
The Vaccine Card at the Sound Choice Pharmaceutical Institute (SCPI) website lists over 21 vaccines and medical products that contain aborted fetal cell lines. The Card is updated yearly, and also lists ethical vaccine alternatives when there are any.
SCPI is a biomedical research organization headed by Theresa Deisher, who has a PhD in Molecular and Cellular Physiology from Stanford and 23 patents in the field to her name. Dr. Deisher, the first person to identify and patent stem cells from the adult heart, has an insiders understanding of genetic engineering having worked in the industry leaders such as Amgen, Genetech, and Repligen.[7]
Among other things SCPI “promotes awareness about the widespread use of fetal human material in drug discovery, development and commercialization.”
No vaccine product is completely pure: “You will find contaminating DNA and cellular debris from the production cell in your final product. When we switch from using animal cells to using human cells we now have human DNA in our vaccines and our drugs.”[8]
The problem is three-fold. Aborted fetal parts are used for experiments, aborted fetal cell lines are used, and fetal cellular DNA debris are in vaccines and medicines.
But it is not just human DNA that is left over, so are some of the chemical stabilizers that keep the product from degrading, as well as, stimulants to rev up the immune system.
“Vaccines are a virus that have been put into a vial, in a liquid, which is the buffer, which we call excipients, and companies have put in stabilizers so that the virus won’t degrade and other things that kind of rev up your immune system so that they can use lower amounts of the virus and have a greater profit margin. And immune stimulants are things like aluminum and thimerosal, they are stabilizers but they rev up the immunes system, so all of these things are in the final product, including contaminates from the cell lines that are used to manufacture the vaccines.”[9]
Why aren’t the contaminates removed? Because nobody wants a pediatric vaccine that costs a few thousand dollars.[10]
In finance, the yield is inversely related to the price. In chemistry, the yield is inversely related to purity. The price of inexpensive mass-produced vaccines is that the medical establishment accepts that the vaccines contain a high amount of fetal contaminates.
“[I]f they have purified out the containments from the cell lines, the yield would be so low that they wouldn’t make any money, or no one would pay a thousand dollars or ten thousand dollars for a vaccine. And so because of that case remnants from the cell lines, in that case, fetal cell lines are in the final product. And they are at actually very high levels. And in the chicken pox, the fetal DNA contaminates are present at twice the levels of the active ingredient which is Varicella DNA.”[11]
Much research is currently being done with fetal cells.
We know this because, for one, there’s a market for fetal parts. In a series of undercover videos, David Daleiden of The Center for Medical Progress exposed Planned Parenthood abortion clinics selling fetal parts to investigators posing as and medical researchers. And for his efforts his office was raided in 2016 by then California Attorney General Kamala Harris, now a Senator and 2020 Presidential Candidate Harris.[12] Daleiden is currently being pursued in court by current California Attorney General, and former Democrat California Congressman, Xavier Becerra.
We already knew this was happening from the testimony of scientists themselves. On January 11, 2018, professor emeritus Dr. Stanley Plotkin, the lead developer of the Rubella vaccine for the Wistar Institute (Philadelphia) in the 1960s, was deposed as an expert witness on Vaccinology in a Michigan child custody case.[13] Dr. Plotkin was asked how many aborted fetuses he has used in his experiments:
QUESTION: So in your, in all of your work related to vaccines throughout your whole career, you’ve only ever worked with two fetuses?
PLOTKIN: In terms of making vaccines, yes.
But after being presented with Exhibit 41 (Proceedings of the Society of Experimental Biology and Medicine), the two fetuses involved in his experiment grows exponentially to 76 aborted fetuses.
QUESTION: So this study involved 74 fetuses, correct?
PLOTKIN: Seventy-six.
QUESTION: And these fetuses were all three months or older when aborted, correct? PLOTKIN: Yes.
A true enough response. Fetal cells, for that matter all normal cells, have a finite capacity to replicate following the principle of cellular aging. The vaccine trail needed many cell lines in order to achieve its end.
An interesting aside, during questioning Dr. Plotkin answered affirmatively that some of his subjects for experimental vaccine trials had been children of “mothers in prison,” the mentally ill, and “individuals under colonial rule” [Belgian Congo].
Dr. Theresa Deisher first became aware of the introduction of fresh aborted fetal material in drug discovery in 1996.[14] Fresh fetal parts are a time-saver compared to the days spent washing and prepping animal tissue, like monkey hearts, for laboratory experiments. While it is not legal to sell aborted fetal tissue, it is still available in catalogues and comes with high prices for shipping and handling.
According to Dr. David A. Prentice Vice, President of the Charlotte Lozier Institute and Adjunct Professor of Molecular Genetics at the John Paul II Institute, adult stem cells are the benchmark for research that has led to actual cures for patients.
“The superiority of adult stem cells in the clinic and the mounting evidence supporting their effectiveness in regeneration and repair make adult stem cells the gold standard of stem cells for patients.”[15]
Then why are we still using embryonic cell lines when adult stem cells have become the Gold Standard? There seems to be little excuse for products that use aborted fetuses.
On the 20th Anniversary of Roe v. Wade in 1993, President Clinton signed five abortion-related memorandums which included the reversal of the George H. W. Bush era moratorium on creating new fetal tissue for research, claiming at the time that, “This moratorium has significantly hampered the development of possible treatments for individuals afflicted with serious diseases and disorders, such as Parkinson’s disease, Alzheimer’s disease, diabetes and leukemia.”[16]
While a bio-ethics debate transfixed the country in 2006 as to whether the United States would allow the use of new aborted fetal stem cells in research, [see White House Fact Sheet on Stem Cell Research Policy], the medical research community had already decided that the future lay with human-animal hybrids and new aborted fetal cell lines. According to a statement submitted to the President’s Bioethics Council:
“Aborted human DNA in our vaccines is not the end, it is only the beginning, as the creation of human-animal hybrids demonstrates. A new aborted fetal cell line has been developed, called PerC6, and licenses have been taken by over 50 partners, including the NIH and the Walter Reed Army Institute, to use this cell line for new vaccine and biologics production. The goal of the company that created the PerC6 is to become the production cell line for ALL vaccines, therapeutics antibodies, biologic drugs and gene therapy.”[17]
And this has largely come to pass.
In 2019, the Department of Health and Human Services granted a second 90-day extension to a contract it has with the University of California at San Francisco that requires UCSF to make “humanized mice” for on-going AIDS research. The human fetal tissue comes from late-term abortions.
CNSNews reported that “according to an estimate it has published on its website, the National Institutes of Health (which is a division of HHS) will spend $95 million this fiscal year alone on research that–like UCSF’s “humanized mouse” contract–uses human fetal tissue.”[18]
See here for news on how the Trump administration limited the sale of fetal parts.
Stop Ebola? Prevent Zika Virus? Cure AIDS? Look for more, not fewer, aborted fetal products in the future.
Writer Andrea Byrnes was the first producer of U.S. March for Life coverage at EWTN Global Catholic Network, which she continued to supervise for seven years. She attended her first HLI conference in 1989, where she first met Servant of God Dr. Jerome Lejeune. She and her husband would later pray for Lejeune’s intercession for her son’s health difficulties discovered before birth, and thanks be to God, he is thriving.
[1] Melanie Warner, “Pepsi’s Bizarro World: Boycotted Over Embryonic Cells Linked to Lo-Cal Soda.” CBS News Moneywatch. June 3, 2011.
[2] Melanie Warner, “Food Companies Test Flavorings That Can Mimic Sugar, Salt or MSG” New York Times. April 6, 2005.
[3] Melanie Warner, “Food Companies Test Flavorings That Can Mimic Sugar, Salt or MSG” New York Times. April 6, 2005.
[4] PepsiCo to Debi Vinnedge Executive Director, Children of God for Life. April 26, 2012.
[5] Christ Young, “San Diego Company’s New ‘Sweetness Enhancer’ Draws Scrunity.” Inewsource. KPBS.Org. October 8, 2015
https://www.kpbs.org/news/2015/oct/08/san-diego-companys-new-sweetness-enhancer-draws-sc/
[6] Valerie Robinson, “Aborted fetus cells used in beauty creams.” The Washington Times. November 3, 2009.
https://www.washingtontimes.com/news/2009/nov/3/aborted-fetus-cells-used-in-anti-aging-products/
[7] Theresa A. Deisher, Phd. “Testimony on Conscience Rights related to biologic drug disclosure and alternative drugs.” President’s Council on Bioethics Archive. Georgetown University. September 8, 2008.
[8] Theresa A. Deisher, Phd. “Testimony on Conscience Rights related to biologic drug disclosure and alternative drugs.” President’s Council on Bioethics Archive. Georgetown University. September 8, 2008.
[9] “Dr. Theresa Deisher Guelph, Ontario Canada June 23, 2018.” Vaccine Choice Canada published on YouTube. August 2, 2018.
[10] The National Vaccine Injury Act was signed in 1986 so that manufactures wouldn’t raise the price of vaccines due to injury lawsuits. Robert Pear, “Reagan Signs Bill on Drug Exports and Payment for Vaccine Injuries.” New York Times. November 15, 1986. https://www.nytimes.com/1986/11/15/us/reagan-signs-bill-on-drug-exports-and-payment-for-vaccine-injuries.html
[11] “Dr. Theresa Deisher Guelph, Ontario Canada June 23, 2018.” Vaccine Choice Canada published on YouTube. August 2, 2018.
[12] Paige St. John. “Kamala Harris’ support for Planned Parenthood draws fire after raid on anti-abortion activist. Los Angeles Times. April 7, 2016.
https://www.latimes.com/politics/la-pol-kamala-harris-planned-parenthood-20160407-story.html
[13] DEPOSITION OF STANLEY A. PLOTKIN, M.D.CASE # 2015-831539-DM, JANUARY 11, 2018, COUNTY OF OAKLAND CIRCUIT COURT, FAMILY DIVISION, MICHIGAN. Ricardo Beas — RBWorks© — Natural Law Church of Health and Healing© © Common Law Copyright – All Rights Reserved, Without Prejudice.
http://www.cafepeyote.com/files/Plotkin_Deposition_-_Summary.pdf
“King of Vaccines Comes Clean!” The HighWire with Del Bigtree. Youtube. Published. January 17, 2009.
[14] Dr. Theresa Deisher: Moral Vaccine Development. Saint Michael Broadcasting. YouTube. Published March 5, 2011.
[15] Wesley J. Smith. “Adult Stem Cells Now the “Gold Standard.” National Review. March 15, 2019. 2:40 PM.
https://www.nationalreview.com/corner/adult-stem-cells-now-the-gold-standard/
[16] Robin Toner. “Settling In: Easing Abortion Policy; Clinton Orders Reversal of Abortion Restrictions Left By Reagan and Bush.” New York Times. January 23, 1993.
[17] Theresa A. Deisher, Phd. “Testimony on Conscience Rights related to biologic drug disclosure and alternative drugs.” President’s Council on Bioethics Archive. Georgetown University. September 8, 2008.
[18] Terence P. Jeffrey. “HHS Extends Contract to Make ‘Humanized Mice’ With Aborted Baby Parts for Another 90 Days.” CNSNews. March 1, 2019. 5:16 PM.
https://www.cnsnews.com/news/article/terence-p-jeffrey/hhs-extends-contract-make-humanized-mice-aborted-baby-parts-another?fbclid=IwAR0NpDMb6W3BVweC0-H4TUza6Ix2aMyjoTn6cOvSmJ9e0YfLk7C6WLueqMwTags: baby body parts, stem cell research
By Gareth Iacobucci British Medical Journal BMJ 2021; 374 doi: https://doi.org/10.1136/bmj.n2086 (Published 20 August 2021) Cite this as: BMJ 2021;374:n2086 Transparency advocates have criticised the US Food and Drug Administration’s (FDA) decision not to hold a formal advisory committee meeting to discuss Pfizer’s application for full approval of its covid-19 vaccine. Last year the FDA […]
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https://www.afinalwarning.com/529750.html
Today’s Situation Update podcast covers a lot of breaking news on world events, including:
In addition, the last section of the podcast discusses the “what if” possibility that at least some covid vaccines may contain exotic technology that, once injected into the body, activates a self-assembly process to build a biocircuitry interface using elements from the victim’s own blood.
Although this sounds like science fiction, we seem to be living in a dystopian sci-fi scenario with biological weapons, magnetic nanoparticle “magnetofection” technology, Orwellian surveillance and all-out government propaganda to coerce everyone into taking a depopulation spike protein injection. (So don’t tell me ANY theory is “out there.”
This is 2021. Global depopulation extermination is under way. Our entire reality is now “out there.”) In addition, the Moderna company openly describes their vaccine injections as installing an “operating system,” which by definition means a platform to receive additional commands or instructions for execution. How are those commands received? From external electromagnetic waves?
Dr. Peter McCullogh has described vaccine-pushing doctors as being in a kind of mind-controlled trance. His exact words from a recent interview: (emphasis added)
What we have learned over time is that we could no longer communicate with government agencies. We actually couldn’t communicate with our propagandized colleagues in major medical centers, all of which appear to be under a spell, almost as if they’ve been hypnotized… Good doctors are doing unthinkable things like injecting biologically active messenger RNA that produces this pathogenic spike protein into pregnant women. I think when these doctors wake up from their trance, they’re going to be shocked to think what they’ve done to people…
Here’s the video where he states this: https://www.brighteon.com/embed/58437760-a8fa-4872-9ad9-0bbba33e5a95
What if it isn’t a spell or a trance but rather a self-assembled, embedded biocircuit that has taken control over their neurology?
What if some vaccines are simple spike protein bioweapons injections, but other vaccines are designed to place people in a kind of “trance” where elements of their neurology are controlled through external signals and commands?
Never forget this published research: Superparamagnetic nanoparticle delivery of DNA vaccine. (PubMed link). It explains: The efficiency of delivery of DNA vaccines is often relatively low compared to protein vaccines. The use of superparamagnetic iron oxide nanoparticles (SPIONs) to deliver genes via magnetofection shows promise in improving the efficiency of gene delivery both in vitro and in vivo.
That same study reveals the only two elements necessary to create “SPIONS” (magnetic nanoparticles) are Iron and Oxygen, both present in human blood: We describe the production of Fe3O4-based SPIONs with high magnetization values (70 emu/g) under 15 kOe of the applied magnetic field at room temperature… Polyethylenimine was chosen to modify the surface of SPIONs to assist the delivery of plasmid DNA into mammalian cells due to the polymer’s extensive buffering capacity through the “proton sponge” effect.
Although this isn’t the same as a self-assembling nanotech biocircuitry system, it hints at the existence of exotic technologies that are exploring such approaches to controlling neurology via external influences (such as electromagnetic fields).
If such technology exists and is being deployed right now, it would explain the seeming “hypnosis” or “trance” under which millions of people now seem to suffer as they continue to demand more bioweapons injections into children and pregnant women. Perhaps there is a simpler explanation, however.
Perhaps today’s doctors are just brainwashed, gullible cowards who care nothing if they harm or kill billions of people as long as they don’t lose their lucrative medical salaries.
Will people ever wake up from this trance and realize they’ve become vaccine murderers?
Nobody knows… Learn more in today’s bombshell Situation Update podcast: Brighteon.com/41404368-f451-4c8a-b16b-7d158a81d317 https://www.brighteon.com/embed/41404368-f451-4c8a-b16b-7d158a81d317
Find a new podcast each weekday at: https://www.brighteon.com/channels/hrreport
Section 23 Fraud Scheme <section23fraudcase@gmail.com>Stored with zero-access encryption
Inbox 9:57 AMTo:
As I lay there on the cardboard that I had put down on the floor of the storage unit I had trouble holding back my tears. I knew that I had to put on a happy face because two beautiful young people needed to know that even though we were now homeless and living in a small storage container, having just moved out of the shelter, that we can never lose hope.
I knew that no matter what we were going through we could never fathom the idea of defeat nor surrender. Little did that mean to two little girls as they lay there on the cold hard ground wrapped up in the remnants of their only clothes we were able to grab when we were being evicted at gun point.
The thoughts of what kind of father am I to have my daughter’s sleeping in a cold storage unit when just a while ago they has their own rooms and their favorite toys and stuffed animals safely surrounding them as they lay sleeping.
My daughter’s grew to understand that in order to change the bad in the world we must sometimes make sacrifices. They saw that the people who took their childhood memories were also the same evil wicked beings that made a number of other elderly handicapped seniors homeless.
My name is Mr. Albert Robinson and I uncovered the longest running fraud scheme in the history of the U.S.
Because I reported it the people involved stole our home and my daughters’ memories but my hardest fight, the fight that I battle everyday, is the fight to never give up hope of bringing all of them to justice.
That is my quest and that is what the books and movie are going to be about.
Thank you. Happy Father’s Day.
June 9, 2021
Bill Maher used to be one of the most influential leftists in the Fake News Media.
But lately he has been sounding more like a conservative as the Left has become more radicalized.
And Bill Maher stunned leftists into silence when he attacked them for pushing useless college degrees.
Just a couple years ago, conservatives absolutely despised Bill Maher.
He is crude and speaks his mind, which used to be filled with nonsensical leftist rants.
Maher would always take cheap shots at Donald Trump’s rhetoric while ignoring his actual achievements and policy goals.
But something has changed recently.
His monologues have gone from promoting leftist causes to calling out their sacred cows.
And his latest monologue had leftists up in arms.
One of the Left’s most cherished institutions is higher education as they control the vast majority of colleges and universities in the country.
So when they heard Maher ripping colleges to shreds they weren’t happy.
Maher first started out by saying that Biden’s American Families Plan believes “that the more time humans spend in classrooms, staring at blackboards, the better.”
He then kicked it into high gear claiming “[l]iberals see more school the way Republicans see tax cuts – as the answer to everything. We imagine going to college as the way to fight income inequality, but actually, it does the reverse.”
He continued, “the unemployment rate of college grads is about half what it is for high school grads. Is it really liberal for someone who doesn’t go to college and makes less money to pay for people who do go and make more?”
Later on in his attack on the Left’s love obsession with higher education, Maher asked “[w]hy is China kicking our ass? Because in 2019, we issued more undergrad degrees in visual and performing arts than in computer and information science or math.”
You can see his full monologue below:
Maher didn’t disappoint with this rant that had leftists’ heads exploding.
People with a conservative mindset are being denied “the space to go speak,” Pompeo said. Source: Pompeo says clampdown on free speech on college campuses scares him more than any other issue
Pompeo says clampdown on free speech on college campuses scares him more than any other issue — Truth2Freedom’s Blog
Photo by: Deborah Williams
In this undated photo provided by Deborah Williams, a Vervet monkey is seen in Dania Beach, Fla. Williams, is the lead author of a study that determined where a colony of monkeys that has lived for about 70 years in urban South Florida came from. In 1948 a group of monkeys escaped from the Dania Chimpanzee Farm. Most were captured, but some disappeared into the mangrove swamp. The study determined that 41 descendants live in the area today. (Deborah Williams via AP) FILE
By Ryan Lovelace – The Washington Times – Wednesday, June 2, 2021
https://www.washingtontimes.com/news/2021/jun/2/human-animal-blending-sparks-lawmakers-fears-frank/
Researchers conducting human-animal hybrid experiments struck fear into federal lawmakers worried that nightmare scenarios of Frankenstein creatures have become a reality.
Earlier this year, researchers announced a blending of man and monkey.
The Salk Institute for Biological Studies in La Jolla, California, said in April that it participated with a China-led research team in an experiment by injecting human stem cells into monkey embryos. They allowed the resulting creature to live and grow for 19 days before terminating it. The researchers responsible for the technology used in the experiment said their work aided the study of embryonic development.
Sen. Mike Braun, Indiana Republican, said he is worried that such human-animal hybrid experiments will cross ethical boundaries and contravene the dignity and sanctity of human life.
“I mean, any of us could speculate on kind of the Frankenstein concept, let’s put it that way, which that was being referred to as in terms of what this leads to,” Mr. Braun said. “I don’t know. I think that I do believe that there’s a genuine interest in taking so much that we’ve learned through DNA analysis, understanding the genome of not only human beings but other animals, that there’s going to be that [temptation] contagion to go beyond maybe, just the altruistic effort of finding cures for very, very vexing ailments like ALS, like Alzheimer’s, like any of the diseases that are out there that are significant, that we’re not even to the point where we know exactly what causes it, let alone cures.”
Mr. Braun and fellow Republicans seek to outlaw chimeras involving the blending of human embryos with animal wombs and animal embryos with human wombs.
Now that a “chimera” is no longer an ancient mythological creature having parts of a lion, goat and serpent, but an actual human-animal hybrid, Republican lawmakers want to establish baselines for American research rooted in a belief in the dignity of human life.
Mr. Braun and Sens. James Lankford of Oklahoma and Steve Daines of Montana sought to amend the Senate’s massive research and development spending bill last week to block certain human-animal chimeras, but the amendment failed by a 48-49 vote along party lines. Three senators did not vote.
Two absent Republicans — Sens. Marsha Blackburn of Tennessee and Thom Tillis of North Carolina — could not have changed the outcome, Mr. Braun said. Senate Majority Leader Charles E. Schumer, New York Democrat, would have blocked a vote on the amendment or ensured that Sen. Joe Manchin III of West Virginia, who also did not vote, would have joined the rest of the Democratic Caucus, he said.
Mr. Lankford said he thought blocking human-animal blending ought to have passed by a voice vote and was shocked to find Democratic opposition.
“We thought it was important to be able to put a stake in the ground and say, ‘No. The United States does not believe it is right to be able to do the blending of animals and humans for experimentation or to try to develop that and ultimately, as China’s on a path to be able to do, to try to implant and grow to a child,’” said Mr. Lankford. “That’s an entirely different direction.”
Mr. Braun, Mr. Lankford, five other senators, and 25 House members led by Rep. Chris Smith, New Jersey Republican, wrote to the National Institutes of Health last week to raise concerns on the chimera research and request details about any ethical analysis the federal agency is pursuing.
The NIH did not respond to the lawmakers but has sponsored a review of ethical questions involving human-animal chimeras. The NIH and the Dana Foundation funded a study published in April by an ad hoc committee of the National Academies of Sciences, Engineering and Medicine to examine the ethical, regulatory and scientific issues associated with neural chimeras and neural organoid research.
The ad hoc committee included a member from the Salk Institute, which participated in the human-animal hybrid experiment. Another Salk Institute researcher oversaw the study. The report concluded that human-animal hybrid experimentation held potential benefits, but researchers should use words that do not attract the general public’s attention.
“The term ‘chimera’ is used because it is scientifically accurate, and the committee believes that its connection with the monsters of ancient myths is too remote to warrant avoiding its use,” said the report, titled “Emerging Field of Human Neural Organoids, Transplants, and Chimeras: Science, Ethics, and Governance.” “Research scientists and their institutional representatives can be cautioned to avoid terminology that may court attention but does their work a disservice by stimulating concerns that go far beyond the current state of the science.”
NIH did not answer The Washington Times’ questions about the study it sponsored, but an NIH spokesperson noted in an email the moratorium on federal funding involving chimera research.
The report avoided making recommendations but listed findings of potential benefits of chimera research to include knowledge of brain diseases that had potential application in the treatments of Alzheimer’s disease, Parkinson’s disease, psychiatric diseases and other ailments.
The report said some studies of human-animal hybrid experimentation surrounding the brain, involving neural chimeras, created concerns about “animals acquiring attributes that could be viewed as distinctly human, or humans taking on roles that should be reserved for a deity.”
Republican lawmakers who are worried about human-animal hybrids say scientists should not play God. Mr. Lankford said scientific experimentation on animals is one matter but attempting to create new forms of life goes too far.
“There’s a real difference in taking human cells and injecting them into a mouse for cancer research and for other research. That’s been done, and it’s been done for a very long time, and we’ve had time to be able to process that,” said Mr. Lankford. “But trying to be able to create life is a very different threshold for me.”
Democrats say Republican opponents of the experiments are following ideology instead of science. Sen. Patty Murray, a Washington Democrat who spoke on the Senate floor last week, said Republican efforts to outlaw chimera research undermine the development of treatments and lifesaving organ transplants.
“If we are serious about bipartisan commitment to American innovation, we’ve got to stop these ideological attacks on medical research and focus on the science and ultimately the health of our patients,” Ms. Murray said.
Mr. Braun, Mr. Lankford, Mr. Daines and Republican Sens. Joni Ernst of Iowa and James M. Inhofe of Oklahoma proposed the failed amendment outlawing certain chimeras.
Mr. Braun said he does not expect Democrats controlling the Senate to allow the legislation to advance.
If he gets the opportunity, he said, he expects pro-life advocates to help draw attention to the issue of human-animal blending. Senators have touted support for their actions from pro-life advocates at the Family Research Council, the Susan B. Anthony List, National Right to Life, the United States Conference of Catholic Bishops and others.
Mr. Braun said he does not expect the Biden administration to listen to his concerns as the NIH reviews restrictions and developments for chimera research, but he wants the agency to know that some lawmakers are watching their moves closely.
It is no understatement to say that the covid 19 phenomenon has been the most momentous event of the 21st century. Bigger even than 911 of 2001, due to its worldwide scope and universal intrusion into the lives of the global population. The world has been forced to conform to its dictates of mask wearing, social distancing and lockdowns, and redefining how we relate to each other on a personal level (for example precluding such basic established human behavior as handshakes). It has effected every aspect of our lives. So its much bigger in scope than the 911 psy-op. 911 was social engineering applied primarily to the US. Covid 19 represents social engineering on a global scale.
And yet the immensity of the event has very little to do with the size of the covid disease threat itself, which in the scheme of the history of pandemics, is not really…
View original post 373 more words
By Cam Edwards | Jun 09, 2021 7:30 PM ET Share Tweet
https://bearingarms.com/camedwards/2021/06/09/biden-background-checks-reality-check-n46336
The odds of the Senate approving the legislation expanding background checks passed by the House earlier this year was never good. Senator Joe Manchin of West Virginia had already said he wasn’t in favor, and there aren’t ten Republican votes in the Senate to pass the bills, much less eleven, which would be the magic number since Manchin’s not on board. Instead, Joe Biden has been betting that talks between GOP senators like John Cornyn of Texas and Chris Murphy of Connecticut would lead to some sort of compromise bill that could get 60 votes in favor, but the Wall Street Journal is throwing some cold water on that idea.
“Progress would probably be overstating it,” Sen. Pat Toomey, a Pennsylvania Republican who has been a key part of the discussions, said of the group’s efforts. Mr. Toomey said that while he might be able to reach a deal with Democrats, he was skeptical they could find nine other GOP votes in the evenly divided Senate. “It’s not clear to me that we get 60 at this point,” he said.
Lawmakers said the recent discussions have centered on expanding background checks to all commercial sales, the focus of 2013 legislation from Mr. Toomey and Sen. Joe Manchin (D., W.Va.). The Senate narrowly blocked that bill, which would have expanded background checks to all commercial sales, including all sales advertised online and at gun shows. Currently, the checks are needed only for sales by federally licensed dealers.
Democrats said they weren’t ready to call a halt to their efforts. Still, at some point, they will have to decide whether to bring legislation to the floor for a vote, even if it hasn’t secured enough support to pass. Senate Majority Leader Chuck Schumer (D., N.Y.) has said that the chamber may hold a vote on gun legislation this month. Others involved in the talks said that could slip until later this summer as negotiations continue.
Nickelodeon is promoting Pride Month to children with a new video featuring drag queen Nina West, who sings about the meaning of all the colors on the pride flag. In the beginning of their struggle, the LGBTQ only wanted tolerance, and eventually they got that. Then the LGBTQ wanted acceptance of their lifestyle and anti-God platform, […]
Nickelodeon Is Indoctrinating Children During Pride Month With Drag Queen Video Teaching About The Meaning Of Colors Of LGBTQ Pride Flag — Now The End Begins — Truth2Freedom’s Blog
By Jim Hoft
Published June 8, 2021 at 5:55pm
https://www.thegatewaypundit.com/2021/06/hackers-expose-8-4-billion-passwords-post-online-possibly-largest-dump-passwords-ever/
Hackers released data on 8.4 billion passwords this week and posted the information online. This might be the largest dump of passwords online ever.
Surprisingly, this is not making many headlines in the mainstream media.
BGR MSN reported:
Shortly before Apple CEO Tim Cook took the virtual stage at the iPhone maker’s Apple Park headquarters campus for WWDC 2021 on Monday — at which the company unveiled a ton of new software updates, including some major new privacy enhancements — an email landed in my inbox underscoring how critical those privacy features are going to be once they roll out with iOS 15. Basically, there’s been another huge data leak, this time exposing several billion passwords in what just might be the biggest dump of passwords online ever.
This news comes via the team at CyberNews, which reports that a 100GB text file containing a staggering 8.4 billion password entries was just leaked on a popular hacker forum. This data set presumably combines passwords stolen via previous data breaches and leaks, and it’s been dubbed the “RockYou2020” password leak on that hacker forum. That name was apparently chosen, per CyberNews, as a nod to the RockYou data breach from back in 2009, “when threat actors hacked their way into the social app website’s servers and got their hands on more than 32 million user passwords stored in plain text.”
If you’re reading these words, suffice it to say you probably need to change your passwords. Today, even. That’s because this new password leak is comparable in scale to the so-called “Compilation of Many Breaches,” or COMB, that we wrote about earlier this year. That previous compilation was essentially a giant database of more than 3.2 billion email-and-password pairings based on existing data that had been stolen as part of previous breaches and leaks from companies like Netflix and LinkedIn.
This new leaked password dataset, of course, is more than double that previous collection. And when you stop and consider that there are more than 7 billion people in the world, this means that there’s a strong likelihood that one of your myriad passwords is very likely caught up in this leak. CyberNews is recommending that anyone who wants to check and see if their passwords are included in this dataset should visit the CyberNews personal data leak checker or the leaked password checker, where password entries from the RockYou2021 compilation are being uploaded.
“By combining 8.4 billion unique password variations with other breach compilations that include usernames and email addresses, threat actors can use the RockYou2021 collection to mount password dictionary and password spraying attacks against untold numbers of online accounts,” CyberNews notes.
By Jim Hoft
Published June 6, 2021 at 9:53am
IT’S WORSE THAN WE THOUGHT! Fauci and Top US Doctors Caught! They CONSPIRED to Disqualify Hydroxychloroquine as COVID Treatment — MILLIONS DEAD AS A RESULT
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The Gateway Pundit has reported extensively this past year on the effects of hydroxychloroquine in treating the COVID-19 virus.
We knew that the Dr. Tony Fauci and the medical elites conspired to ban the use of this very successful drug.
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We reported earlier on how Dr. Fauci used bogus studies to disqualify HCQ in treating coronavirus.
As previously reported–
It’s been over a year since the WHO declared the coronavirus a pandemic after originally downplaying the threat. It is no secret that both the disease and the response to combat it following this SARS-CoV-2 outbreak in late 2019 have turned our world upside-down. Mandates, lockdowns, and guidelines seem to change every time Dr. Fauci opens his mouth. All of these unprecedented rules were put into place, we were told, to slow down the spread of a disease that today is linked to the death of over half a million Americans and 3.7 million global citizens in the last year.
You would think that researchers would have concentrated on prophylactic and therapeutic solutions of this disease especially since this disease is a death sentence for the elderly, the obese, those with preexisting conditions. The coronavirus doctors have forced children to avoid school, mask up, and get vaccinated. One would think that after all this time there would be a consensus in the hospitals, in the nursing homes, and in other treatment centers on how to treat a Covid positive patient or resident. This is not the case.
There still is no agreed-upon treatment plan for elderly patients who catch coronavirus to assist in their recovery.
The CDC and Dr. Fauci ignored treatment plans for coronavirus patients unless the person was under severe distress.
Cardiologist and Professor of Medicine Peter McCullough testified in Texas earlier this year. Dr. McCullough sees COVID patients and says 85% of COVID patients given multi-drug treatment plan recover from the disease with complete immunity. McCullough added, “The pandemic could have been over by now, he says, if those who tested positive for covid had been immediately treated before they fell ill enough to be hospitalized. He also says that thousands could have been, and still could be saved if the treatment protocol he and other physicians use were not suppressed.”
Dr. Fauci and the CDC and WHO suppressed this effective treatment plan and others.
And hundreds of thousands of innocents died.
And now this…
The c19hcq.com website tracks all of the international studies on hydroxychloroquine and its effects on the coronavirus.
There is now a new study and the results are SHOCKING!
— HCQ for COVID-19: real-time meta analysis of 245 studies
HCQ is not effective when used very late with high dosages over a long period (RECOVERY/SOLIDARITY), effectiveness improves with earlier usage and improved dosing. But early treatment consistently shows positive effects. That’s the science.
TGP contributor Larry Johnson touched on this on Wednesday night and took excerpts from Headline USA‘s reports on Dr. Fauci’s emails regarding hydroxychloroquine.
But the e-mails also showed that Fauci was more in the loop than he let on concerning some of the Trump administration’s proposed treatment solutions.
He notoriously second-guessed then-President Donald Trump during a press conference statement about the benefits of using hydroxychloroquine.
Fauci refuted President Trump in a White House press conference on March 25:
Although Fauci seemed taken aback and insisted that the “anecdotal” claims had yet to be conclusively studied, a month earlier he had been looped into an email to Pence on Feb. 29 in which a pair of Oklahoma physicians extensively discussed their research on it.
Fauci also responded to a Feb. 24 inquiry that noted that China had been reporting about its clinical studies with the drug.
“Is there any indication/data to substantiate this claim from China (attached publication) that chloroquine/hydroxychloroquine can decrease COVID-19 infections and lung disease?” wrote Maryland pharmacologist Philip Gatti.
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Fauci’s passive reply echoed what he would later convey on the national stage.
“There are no data in this brief report and so I have no way of evaluating their claim,” he wrote dismissively.
“There are a lot of these types of claims going around,” he continued. “I would love to see their data.”
Then in May Dr. Fauci told CNN that hydroxychloroquine was actually “dangerous” and ineffective.
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Dr. Fauci told CNN hydroxychloroquine was actually dangerous when used as a prophylactic against coronavirus. Hydroxychloroquine had been used safely for 65 years in millions of patients. And so the message was crafted that the drug is safe for its other uses, but dangerous when used for Covid-19.
This statement made headlines throughout the fake new media and it was a complete lie.
After Fauci’s statements on hydroxychloroquine, the tech giants began censoring any mention of the drug. The media mocked President Trump and anyone who suggested the drug was safe and effective. Doctors treating coronavirus patients were suspended from their social media accounts.
And hundreds of thousands of people died.
It was all based on a lie perpetrated by Dr. Anthony Fauci.
* * * * * * * * * *
Now there is more information that it was not just Fauci but all of the top US medical leaders who were in on the hydroxychloroquine lie.
Dr. Meryl Nass, MD, broke this story in The Defender. According to Dr. Nass, the top health officials were all in on the conspiracy against hydroxychloroquine.
Fauci runs the NIAID, Collins is the NIH director (nominally Fauci’s boss) and Farrar is director of the Wellcome Trust. Farrar also signed the Lancet letter. And he is chair of the WHO’s R&D Blueprint Scientific Advisory Group, which put him in the driver’s seat of the WHO’s Solidarity trial, in which 1,000 unwitting subjects were overdosed with hydroxychloroquine in order to sink the use of that drug for COVID.
Farrar had worked in Vietnam, where there was lots of malaria, and he had also been involved with SARS-1 there. He additionally was central in setting up the UK Recovery trial, where 1,600 subjects were overdosed with hydroxychloroquine.
Even if Farrar didn’t have some idea of the proper dose of chloroquine drugs from his experience in Vietnam, he, Fauci and Collins would have learned about such overdoses after Brazil told the world about how they mistakenly overdosed patients in a trial of chloroquine for COVID. The revelation was made in an article published in the JAMA in mid-April 2020. Thirty-nine percent of the subjects in Brazil who were given high doses of chloroquine died, average age 50.
Yet the Solidarity and Recovery hydroxychloroquine trials continued into June, stopping only after their extreme doses were exposed.
Fauci made sure to control the treatment guidelines for COVID that came out of the NIAID, advising against both chloroquine drugs and ivermectin. Fauci’s NIAID also cancelled the first large-scale trial of hydroxychloroquine treatment in early disease, after only 20 of the expected 2,000 subjects were enrolled.
What does all this mean?
Read the rest here.
This is an absolutely huge development!
http://www.dogfoodadvisor.com June 2, 2021 — Sunshine Mills, Inc. is voluntarily recalling multiple dog food products due to potential contamination with Salmonella bacteria. What’s Recalled? The following products were distributed online and in retail stores. The “best by” date and related lot codes can be found on the back of each package. No other Sportsman’s Pride, […]
Sunshine Mills Recalls Multiple Dog Food Brands | Dog Food Advisor — “OUR WORLD”
Friday, June 4, 2021 15:34
3171By Jeffery Pritchett
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2021 NEW Conscious Life Expo… MUST WATCH!!! A very rare video appearance from Dr. Steven Greer discussing how to make contact with ET civilizations. Human Initiated contact: – CE5. How to do it. Why it is important. And how to form your own groups. People from Thailand to Nova Scotia to Russia are doing CE5 with amazing experiences. Father of the Disclosure movement, he presided over the groundbreaking National Press Club Disclosure Event in May, 2001. Over 20 military, government, intelligence and corporate witnesses presented compelling testimony regarding the existence of extraterrestrial life forms visiting the planet, and the reverse engineering of the energy and propulsion systems of these craft. Over one billion people heard of the press conference through the original webcast and on subsequent media coverage on BBC, CNN, CNN Worldwide, Voice of America, Pravda, Chinese media, and media outlets throughout Latin America.
The webcast had 250,000 people waiting online – the largest webcast in the history of the National Press Club at that time. He has worked for 17 years to bring together the scientists, inventors and leaders in society to advance new clean technology energy systems. He is considered one of the world’s foremost authorities on the strategic process of transforming our carbon-based civilization to a long-term sustainable civilization using innovative sciences and technology. A lifetime member of Alpha Omega Alpha, the nation’s most prestigious medical honor society, Dr. Greer has now retired as an emergency physician to work on these projects. He is the author of four insightful books and multiple DVDs on the UFO/ET subject.
He teaches groups throughout the world how to make peaceful contact with extraterrestrial civilizations, and continues to research bringing truly alternative energy sources out to the public. Dr. Greer has studied the Sanskrit Vedas extensively and has been teaching mantra meditation for over 30 years. Dr. Greer has been seen and heard by millions world-wide on CBS, the BBC, The Discovery Channel, the History channel, The Ancient Aliens series, Thrive and through many news outlets worldwide.— His message is one of hope – that these energy systems can soon be available worldwide. His goal is to assist in the creation of a sustainable, peaceful civilization on Earth that is both high tech and in harmony with the environment.
FOLLOW BEFORE IT’S NEWS ON TELEGRAM – https://t.me/BeforeitsNewsHow To Manifest Anything You Desire In Life
Ok, so I went and picked up a special baby. She is AKC Giant Malamute. She is four (4) months old. Her name, when we picked her up was Precious. We know I could not leave it at that, so I named her Native American Name, like all my babies… Quetzalli Kasa, Precious thing dressed in furs. So, I didn’t change her name, I enhanced it.
She was the pick of the litter, that the breeder was planning to keep. She has the mother still. The breeder got the mother a few years ago, she ordered her straight out of Alaska: Kingfishers Baroness Alaska (WS48497307), and the father: Artemis Nox (WS62796509). The ad was on the AKC site: https://marketplace.akc.org/breeder/barbara-akers-30948/alaskan-malamute/265779
The breeder planned to keep her, and she was living with the breeder, both her parents, and her aunt (all 4-legged). The breeder was in some kind of accident and had a brain injury. She decided that she could not take care of all of the animals and first sold the father. Then shortly after that, ran the ad for the puppy. I ran across the ad right after it began running, and contacted her. It is most probably the only breeder in GA of the Giant Malamute. She is very special.
I felt badly about taking the baby, but she assured me that she wanted her to go the best home possible, and that is my house. I called to let her know we had gotten home ok. She said that she had been crying ever since we left. I felt so badly.
It took the puppy a day to get over the travelling and the new place, but, tonight she snapped out of it, and she is fine. “I’m a puppy, puppies play, everything’s a toy, and everything’s a game, cause I’m a puppy and puppies play!” I had forgotten how much fun a very large breed puppy can be. Ouch!
But for everyone that knows the turmoil of loss, and those who know how devastated we were at our loss, and all the kind words, and sympathy, and for all my neighbors that put with Takee howling 20 hours a day for a week, Thank You!
Nothing ever will or ever can bring back Tiponi, and we still miss her tremendously, and I still daily, shed tears from the pain of the loss. She will be in our hearts forever, and if God should accept us into heaven, we will be reunited there. May God hold her in the palm of His Hand forever….
Last night my baby-girl (4-legged), died for no apparent reason. I have to assume she was poisoned. An hour earlier, she was happy and healthy. She laid down and died, and it is breaking my heart! She was eight years old, the date on my camera is wrong. She was born in 01-2013.
Tiponi — Manifest Injustice
By Tucker Carlson Global Research, May 21, 2021 Citizen Free Press 12 May 2021 Region: USA Theme: Science and Medicine
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How many Americans have died after taking the Covid vaccine?
How many Americans have died after taking the COVID vaccines? Not Americans who’ve been killed by the virus, that’s a huge number, but how many Americans have died after getting the vaccines designed to prevent the virus? Do you know the answer to that question? Do you know anything about the downside? We know a lot about the upside of the vaccine. We’ve been completely in favor of vulnerable people taking vaccines.
But what about the potential risks? You’d think you would know more about that than you do. We talk about vaccines constantly, not just on this show, but in this country. Joe Biden was on TV yesterday talking about vaccines. He wants you to get one. Everyone in authority wants you to get one. In fact, you’ve probably already had your shot, and good for you. If you haven’t had your shot, you’re under enormous pressure to get your shot. You understand that soon you may not be able to fly on commercial airplanes or go to work at the office or send your children to school if you don’t have the shot. Meanwhile, the social pressure is enormous. Friends may have already informed you that you’re not welcome at their parties or weddings if you haven’t been vaccinated. There is a lot of pressure to comply. At some point, you probably will comply. It’s just too difficult not be to vaccinated in this country.
Click here to watch the video.
But before you make the appointment: do you know anything about the potential risks? Probably you don’t know much. We all assume the risks are negligible. Vaccines aren’t dangerous. That’s not a guess, we know that pretty conclusively from the official numbers. Every flu season, we give influenza shots to more than 160 million Americans. Every year, a relatively small number of people seem to die after getting those shots. To be precise, in 2019, that number was 203 people. The year before, it was 119. In 2017, a total of 85 people died from the flu shot.
Every death is tragic, but big picture, we don’t consider those numbers disqualifying. We keep giving flu shots, and very few people complain about it. So the question is how do those numbers compare to the death rate from the coronavirus vaccines now being distributed across the country? That’s worth knowing.
We checked today. Here’s the answer, which comes from the same set of government numbers that we just listed: Between late December of 2020, and last month, a total of 3,362 people apparently died after getting the COVID vaccines in the United States. Three thousand, three hundred and sixty-two — that’s an average of 30 people every day. So, what does that add up to? By the way, that reporting period ended on April 23. We don’t have numbers past that, we’re not quite up to date. But we can assume that another 360 people have died in the 12 days since. That is a total of 3,722 deaths. Almost four thousand people died after getting the COVID vaccines. The actual number is almost certainly much higher than that — perhaps vastly higher.
The data we just cited come from the Vaccine Adverse Events Reporting System — VAERS — which is managed by the CDC and the FDA. VARES has received a lot of criticism over the years, some of it founded. Some critics have argued for a long time that VARES undercounts vaccine injuries. A report submitted to the Department of Health and Human Services in 2010 concluded that “fewer than one percent of vaccine adverse events are reported” by the VARES system. Fewer than one percent. So what is the real number of people who apparently have been killed or injured by the vaccine? Well, we don’t know that number. Nobody does, and we’re not going to speculate about it. But it’s clear that what is happening now, for whatever reason, is not even close to normal. It’s not even close to what we’ve seen in previous years with previous vaccines.Tucker Carlson: Know Potential Risks of Coronavirus Vaccines before Getting Vaccinated
Most vaccines are not accused of killing large numbers of people. The Menveo vaccine, for example, is given to people around the world, often children, to prevent bacterial meningitis. In this country, only one person died from that vaccine in the entire period between 2010 and 2015. One. So, compare that to what’s happening now. In just the first four months of this year, the U.S. government has recorded more deaths after COVID vaccinations than from all other vaccines administered in the United States between mid-1997 and the end of 2013. That’s a period of fifteen and a half years. Again, more people, according to VAERS, have died after getting the shot in four months during a single vaccination campaign than from all other vaccines combined over more than a decade and a half. Chart that out. It’s a stunning picture. Now, the debate is over what it means. Again, there’s a lot of criticism of the reporting system. Some people say “well, it’s just a coincidence that someone gets the shot and then dies, possibly from other causes.” No one really knows, is the truth. We spoke to one physician today who actively treats COVID patients. He described what we’re seeing now as the single deadliest mass-vaccination event in modern history. Whatever is causing it, it is happening as we speak. So you’d think someone in authority might want to know what’s going on.
If the vaccine injury reporting system is flawed — and it clearly is flawed — why hasn’t it been fixed? And more to the point, why has there not been an independent vaccine safety board to assess what’s happening. And reassure people who stumble across official government numbers on the internet. But amazingly, none of that has been done. No one even mentions the numbers. And in fact, you’re not allowed to. You’ll be pulled off the internet if you do. The people in charge do not acknowledge them. Instead, they warn us about what might happen if we don’t take the vaccine.
“People who are not fully vaccinated can still die every day from COVID -19,” Biden said. As a factual matter, that is true. But it’s also misleading. Not all Americans are at a similar risk of dying from COVID-19. Some are at relatively high risk: the old and the sick. They might want to get vaccinated, and most do. Some are at very low risk of dying: the young and the healthy. Others appear to be at essentially no risk at all: anyone who’s had COVID and recovered. Virtually all of those people are immune. That’s true for many viruses. Those second two categories — the young and healthy, and the previously infected — may add up to hundreds of millions of people in this country. The funny thing is, the White House – the official policy-makers who are designing the vaccine rollout – do not acknowledge that those categories even exist.
Health Authorities are pretending that everyone’s health and risk potential is exactly the same as everyone else’s. That’s why Joe Biden has demanded that 70 percent of all American adults — regardless of age, regardless of health condition, regardless of pre-existing antibodies — get the COVID shot by the Fourth of July two months from now, or else.
This might be an acceptable policy – it would never be an ethical policy – but it might be acceptable to the country if COVID vaccines we could show conclusively came with no risk, and if we truly understood the long-term effects of those vaccines. But neither one of those things is true. We know that according to the government reporting system, thousands of people have died after getting the shot. That is true in this country, where it’s hotly debated when it’s talked about at all, but it’s also true in European countries, whose record-keeping is, if anything, more reliable than ours. Many thousands of other people appear to have been injured after getting the vaccine. VAERS records nearly 900 non-fatal heart attacks in people who just received the shot. 2,700 people reported unexplained chest pain. In all, the vaccine, according to the government reporting system, appears to have contributed to at least 8,000 hospitalizations.
Some of the side effects defy explanation. Researcher Alex Berenson has noted that coronavirus vaccines now account for almost one-third of all tinnitus reports in the VAERS database. That’s the ringing in your ears. The American Tinnitus Association says it’s received “many questions” on the link.
Researchers at Oxford and UCLA have begun tracking coronavirus vaccine side effects across eight separate countries. They found, that “Women aged 18 to 34 years had a higher rate of deep vein thrombosis than men of the same age.” They also found that heart attacks were “common” in people aged 85 and older who had taken the vaccine. They found serious potential side effects in some children, “anaphylaxis [and] appendicitis were more common in young people.”
Vaccines are complicated medicines, and as with any drug, it can take a long time to get it precisely right. The dosage, for example. And this is not the first time people have been hurt during a vaccination campaign. That is bound to happen. What’s different this time, and so striking, is the reaction to these numbers. Here’s a contrast for you: in 1976, the U.S. government vaccinated 45 million people with a vaccine for the swine flu. Fifty-three people reportedly died after getting that shot. The U.S. government immediately halted the vaccination program. Authorities decided it was too risky, it wasn’t worth it.
Contrast that with what is happening now. This time, our health authorities have reserved their energy for anyone who dares to question vaccines. LifeSiteNews, a nonprofit news organization, just found itself permanently banned from Facebook. Why? Because it reported government numbers from the VAERS database.
When Joe Rogan asked whether healthy young people ought to get the vaccine, the media treated him like a criminal.
Almost everything they said was a lie that obscured a very simple and potentially relevant question that he asked, which is: should healthy young people receive the vaccine? We’re not precisely sure what the risks are. It is a lie to say there are no risks. There are risks in everything, including in getting a vaccine. So why not rationally weigh the risk/reward ratio, as we do with every decision we make. For that, he was denounced as an anti-vaxxer kook. A danger to public safety.
One of the very few elected officials in the country who has said a word about any of this, who has asked the obvious questions, not attacking vaccines, wondering about their effects, is Republican Senator Ron Johnson of Wisconsin. Last week, Johnson asked Francis Collins, the director of the NIH, why so many Americans seem to be dying after the shot.
Maybe there’s a good answer for that, Collins wouldn’t even acknowledge that was happening. Instead, Collins fretted if the population focused too much on the harm from vaccines, people might be hesitant to get them.
“I challenged his use of the term ‘Vaccine Hesitancy,’” Ron Johnson told us in a conversation today. “I told him that based on the VAERS deaths, and my conversations with people who have chosen not to get vaccinated, a better description would be: ‘People who are hesitant to be coerced into participating in the largest drug trial in history.’”
Exactly. There’s a reason many states have more vaccine doses than they can use. Some people just don’t want the vaccine. That’s their right. Period. Not all of them are crazy. Health decisions used to be considered personal choices. We didn’t ask about them. They were considered personal as recently as last fall. In September of 2020, at the height of the presidential campaign, a CNN reporter asked Kamala Harris whether she’d be willing to take the coronavirus vaccine once it became available.
“Well, I think that’s going to be an issue for all of us,” Harris responded. “I will say that I would not trust Donald Trump.” A month later, at the vice presidential debate, Harris was if anything more emphatic on the subject. “If Donald Trump tells us we should take” the vaccine, she declared, “I’m not going to take it.”
Kamala Harris has, of course, since changed her mind. She’s no longer skeptical of the vaccine, nor does she tolerate the skepticism of others. Instead, she’s an enthusiastic participant in COVID theater.
Just today, Harris and her husband made a point of kissing each other in front of photographers while wearing masks. They did this despite the fact they’re married, that they live together, that they were standing outside at the time and despite the fact that they both have been vaccinated.
It doesn’t make you laugh. It makes you nervous. Why are they talking to you that way? Why are they giving you the finger on TV? No matter how many fingers they give you, it doesn’t change what remains true for the country: If American citizens are going to be forced to take this vaccine or any other medicine, they have an absolute right to know what the effects of it might be. And they have an absolute right to ask that question. Without being silenced or censored or mocked or given the finger. No amount of happy talk or coercion or appeals to false patriotism can change that. Period.
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US President Joe Biden removes his face mask as he delivers remarks on the administration’s coronavirus disease (COVID-19) response outside the White House in Washington, U.S., April 27, 2021. © REUTERS / Kevin Lamarque President Joe Biden frantically searched for his mask during a speech in Georgia, telling supporters he was “in trouble,” despite the fact that […]
‘I’m in trouble’: Fully-vaccinated Joe Biden struggles to find mask during outdoor speech (VIDEO) |RT USA News — Truth2Freedom’s Blog
Image by Gerd Altmann from Pixabay
https://pixabay.com/illustrations/syringe-vaccine-cost-corona-4966959/
Since when did they start giving freebies, if you get a vaccine?
Since when do you need more than one vaccine for any virus?
Vaccine means a specially prepared antigen which, upon administration to a person, will result in immunity. https://www.lawinsider.com/dictionary/vaccine
Since when: do vaccines make you sterile? do you need two shots for one virus?
Since when does a virus mutate more than once a year? (I use once a year, because every year, they used to come out with a new flu shot). But wait, how can they have a new flu shot for the new flu, if the flu is new? They can’t. So the yearly flu shot has been bullshit all along too. BUT, they got everyone to believe that they needed a flu shot every year. Now, they want the people to believe that it takes multiple shots within weeks of each other, to immunize people? Since when did that happen? Oh, I know, I know! Since Bill Gates said so.
Image by Clker-Free-Vector-Images from Pixabay
Since when did Bill Gates become a Doctor? Since when did Bill Gates become anything more than a thief, and Microsoft crook, whose daddy was a man working for the people that appear at Bilderberg every year? All of the sudden Bill Gates, the man that said that they planned to cull the human herd through the use of vaccines, creates vaccines. Some of Bill Gates vaccines killed and maimed Africans, people living in India, and now Italians can be added to the countries that want him tried as a war criminal.
Since when do you need to wear a mask for a virus? Only sick people should be required to wear a mask. People believe everything that comes out of the mouth of the likes of Fauci? You can’t tell me that everyone believes the words of someone with little beady eyes, and changes his recommendations as often as he changes his underwear?
Since when do people that have had the vaccine, have to fear people who have not have had the vaccine? Common sense tells us that if we have had the vaccine, that we are immune. So what the hell do you have to fear, except fear itself. Why are you afraid? Because the fake news says to fear? The news is nothing more than a bunch of fear mongers, that are owned by those who plan to cull the human herd. You want to listen to people that want to kill you off? Are you really that gullible?
When I was a kid, all kids got the chicken pox. Once you get it, like any other virus, once you have had it, you can’t get it again, unless you never got the chicken pox. What is everyone so afraid of? It has been proven that the survival rate is like 97.9% survivor rate.
Where has everyone’s common sense gone? Are you not filtering your water to remove the fluoride, chlorine, and other things that are put into the water to dumb you down?
Annamarie Strang
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People really believe the government would not lie to them? People really believe that the government is going to keep them safe? Safe from what? The government has taken over “The People’s House” (the white house). So people really believe that those who are hold up in the White House are going to protect the people from something? It appears more like the people hiding in the White House, with armed military to protect THEM, not the people. And these same people that believe those hiding in the White House, guarded by armed Military, want to protect anyone, except themselves? The White House is the People’s House, and it has been taken over by those who want to stay away from normal every day people.
Our forefathers have already rolled over in their graves because of what “We the People” have turned into. God has warned and warned of the times to come, and here people line up to get their mark of the beast.
I swear, I fail to understand. People would not know a false flag, if it bit them in the ass while waiving a flag, with “false flag” written on it. Democrats don’t care about our lives. They are willing to kill off their underlings to get what they want. They want the country and for you to be slaves, thus they must take the guns of the American people, in order to get what they want. You don’t really think that they would not have a madman kill a bunch of people to cause their underlings to bow down and turn in their guns for fear of being shot during any number of circumstances. Do you really think that they would not kill your kids to make you change? Think again. They will stop at nothing. These very same people that took a knee, that bowed to the Chinese dictator, that do deals with Putin behind your backs?
People that believe these things, are not people, they are sheeple, willing to walk off the edge of the cliff, because of being promised that they will be kept safe. And the government is just the ones that will save them. I gave up on the sheeple awakening. I used to think they would. Apparently, I was wrong.
https://www.eff.org/cases/oracle-v-google
At issue in Oracle v. Google is whether Oracle can claim a copyright on Java APIs and, if so, whether Google infringes these copyrights. When it implemented the Android OS, Google wrote its own version of Java. But in order to allow developers to write their own programs for Android, Google’s implementation used the same names, organization, and functionality as the Java APIs. For non-developers out there, APIs (Application Programming Interfaces) are, generally speaking, specifications that allow programs to communicate with each other. So when you read an article online, and click on the icon to share that article via Twitter, for example, you are using a Twitter API that the site’s developer got directly from Twitter.
In May 2012, Judge William Alsup of the Northern District of California ruled that APIs are not subject to copyright. The court clearly understood that ruling otherwise would have impermissibly—and dangerously—allowed Oracle to tie up “a utilitarian and functional set of symbols,” which provides the basis for so much of the innovation and collaboration we all rely on today. Simply, where “there is only one way to declare a given method functionality, [so that] everyone using that function must write that specific line of code in the same way,” that coding language cannot be subject to copyright.
Oracle appealed Judge Alsup’s ruling to the U.S. Court of Appeals for the Federal Circuit. On May 30, 2013, EFF filed an amicus brief on behalf of many computer scientists asking the Federal Circuit to uphold that ruling and hold that APIs should not be subject to copyright. On May 9, 2014, the Federal Circuit issued a disastrous decision reversing Judge Alsup and finding that the Java APIs are copyrightable, but leaving open the possibility that Google might have a fair use defense.
On October 6, 2014, Google filed a petition asking the U.S. Supreme Court to review the Federal Circuit’s decision. On November 7, 2014, EFF filed an amicus brief on behalf of many computer scientists that asked the Supreme Court to grant Google’s petition for review, reverse the Federal Circuit, and reinstate Judge Alsup’s opinion. Unfortunately, in June 2015 the Supreme Court denied Google’s petition.
The case returned to the district court for a trial on Google’s fair use defense. Fortunately, in May 2016, a jury unanimously agreed that Google’s use of the Java APIs was fair use. Oracle filed another appeal. In May 2017, EFF (along with Public Knowledge) filed an amicus brief asking the Federal Circuit to affirm the jury’s verdict. However, in March 2018, the Federal Circuit reversed the district court again, in a decision that made even less sense than its 2014 opinion. The Court rejected the jury’s verdict (after previously saying that the jury had to decide the case), and held that Google’s use was not a fair use as a matter of law. Google petitioned the entire Court to rehear the case, and EFF filed an amicus brief supporting Google’s petition. The Federal Circuit denied Google’s petition in August 2018.
In January 2019, Google filed another petition asking the U.S. Supreme Court to review both Federal Circuit decisions. EFF filed an amicus brief supporting Google’s petition in February 2019. In November 2019, the Court granted Google’s petition; EFF filed an amicus brief supporting Google on the merits. The Court heard oral argument in October 2020. (One procedural note: because of the Supreme Court’s rules on citing cases, the lawsuit will now be known as Google v. Oracle, since Google asked the Supreme Court to hear the case. After nine years, we’ll have to get used to calling the case by this new name.)
In April 2021, the Court issued an opinion reversing the Federal Circuit and holding that Google’s use of the Java APIs was fair use as a matter of law. The Supreme Court’s ruling represents a victory for programmers, developers, and other users who want to use their acquired knowledge and experience with software interfaces in subsequent platforms.
By Jim Campbell May 17th, 2021 Earlier today Arizona GOP Chairwoman Kelli Ward noted the Maricopa Board of Supervisors (BoS) was engaging in a propaganda war against the people of Arizona and the State Senate. It didn’t take long for evidence to surface. The Board of Supervisors sends the media a copy of the 13-page […]
Resolving the Arizona Forensic Ballot Audit — Jim Campbell’s
by Tyler DurdenTuesday, May 18, 2021 – 12:10 AM
Due to their counterculture connotations and rigid legal status, psychedelics were once considered a highly stigmatized topic.
Over the last decade however, a steady stream of groundbreaking research has proven that these powerful substances have the potential to safely treat a wide range of diseases.
Today, attitudes toward the industry have changed, and capital is flowing- resulting in a market that analysts predict could eventually be worth $100 billion.
The graphic above from Tryp Therapeutics is the first in a two-part series that explores how psychedelics have evolved over the last 6,000 years.
Before we dive into the history of psychedelics, it’s important to understand what they are and how they work.
Psychedelics are drugs that alter cognitive processes and produce hallucinogenic effects. Broadly speaking, there are two categories that psychedelic substances fall into: entheogens, and synthetic drugs. Entheogenic psychedelics are derived from plants, while synthetic psychedelics are created in a laboratory.
Here are some of the most well known psychedelic substances explained:
Certain psychedelics work by binding to serotonin receptors in the brain which produces psychoactive effects. Research suggests that when this happens, the structure of the brain changes—such as the number of connections between neutrons. This means that psychedelics could have the potential to rewire or repair circuits in the brain, hence their reputation for having healing powers.
While the science behind these mind-altering plants is only now beginning to become clear, they have in fact been used in rituals and ceremonies for thousands of years.
As a result, psychedelic substances have been hugely influential in shaping certain cultures and religions dating back to 4,000 BC. These cultures, particularly in the Americas, learned how to utilize psychoactive plants and mushrooms for medicinal purposes or to reach an altered state of consciousness.
With that being said, evidence of how psychedelics were used in ancient times is often anecdotal, and therefore widely debated.
In the 1800s, scientists and psychiatrists began discovering new kinds of drugs such as psilocybin and subsequently became advocates of psychedelic medicine. Unfortunately, uncontrolled drug use for recreational purposes led to governments across the world debating their legal status, and clamping down on restrictions.
Within decades, the recreational use of psychedelics undermined promising medical discoveries, and put the future of the industry into question, eventually triggering the War on Drugs.
With these strict legal changes around the world, the psychedelics industry became largely inactive. But today, an explosion of unprecedented research findings surrounding the therapeutic potential of psychedelics has triggered many countries to reassess their decision to criminalize.
Now, the industry is back, and bigger than ever before. In Part 2 of The History of Psychedelics, we’ll dive into The Psychedelics Renaissance the industry is currently experiencing and discuss the exciting future of this promising sector.9,39135
74Oversight Committee / YouTubehttps://imasdk.googleapis.com/js/core/bridge3.453.0_en.html#goog_187019551Volume 90% PENNY STARR22 Apr 20215772:57
Swedish teen climate activist Greta Thunberg lashed out at members of Congress at a House Committee on Oversight and Reform Subcommittee on the Environment hearing on Thursday, telling representatives they won’t get away with ignoring the so-called climate crisis.
“I know I’m not the one who is supposed to ask questions here but there is something I really do wonder,” Thunberg, who is 18, said. “How long do you honestly believe that people in power like you will get away with it?”
“How long do you think you can continue to ignore the climate crisis, the global aspect of equity, and historic emissions without being held accountable,” Thunberg said.
The activist, who refused to fly to the United States to attend a United Nations climate change summit in 2019 and instead traveled in a sailboat made, in part, from fossil fuel products, went on to say young people like her will be in charge of politicians’ legacies.
“You get away with it now, but sooner or later, people are going to realize what you have been doing all this time,” Thunberg said. “That’s inevitable. You still have time to do the right thing and save your legacies.”
“But that window of time is not going to last for long,” Thunberg said. “What happens then?”
“We the young people are the ones who are going to write about you in the history books,’ Thunberg said. “We are the ones who get to decide how you will be remembered.”
“So my advice to you is choose wisely,” Thunberg said.
The hearing focused on how tax benefits to fossil fuel entities are hampering the fight against climate change and should be abolished. Only one witness on the five-person panel at the hearing represented the fossil fuel sector and its stakeholders.
Frank Macchiarola, senior vice president of Policy, Economics, and Regulatory Affairs of the American Petroleum Institute, took blistering questions from Democrats who support stripping tax benefits from fossil fuel entities in President Joe Biden’s plan, promoted as infrastructure legislation.
Thunberg called the need for the hearing “a disgrace.”
“The fact we are still having this discussion, and even more, that we are still subsidizing fossil fuels directly or indirectly using taxpayer money is a disgrace,’ Thunberg said.
Thunberg gained the spotlight several years ago when she founded Fridays for Future urging young people to leave school and protest on Fridays to advance the climate change agenda.
“The simple fact and uncomfortable fact is that if we are to live up to our promises and commitments in the Paris Agreement, we have to end fossil fuel subsidies, stop new exploration and extraction, completely divest from fossil fuels, and keep the carbon in the ground,” Thunberg said.
Follow Penny Starr on Twitter or send news tips to pstarr@breitbart.com
Originally posted on Counter Information: By Dr. Joseph Mercola Global Research, March 31, 2021Mercola I’ve discussed why COVID-19 vaccines are in fact gene therapies and not vaccines in several previous articles, including “COVID-19 mRNA Shots Are Legally Not Vaccines,” “COVID-19 ‘Vaccines’ Are Gene Therapy” and “How COVID-19 ‘Vaccines’ May Destroy the Lives of Millions.” However, despite…
COVID-19 Vaccines Likened to ‘Software Updates’ for Your Body — The Most Revolutionary Act
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