Pharma Day Quotes

Pharmaceutical companies raked in billions by forcing all kinds of pills down the throats of the ill-informed populace. So in light of these facts, his prank call could’ve been considered a wake-up call, as millions of people were swallowing their prescribed pills every day, relying on supposedly safe drugs to perpetually put off their mental issues instead of facing them head on and resolving them for good. Not only did these drugs that were labeled legal and effective mask issues, but they also made people’s mental issues worse.

A Smoothie a day keeps Big Pharma away

Sixth of Ten Elegies for Fire and Oxycodone The Greek myth goes like this you probably know it but I had to look it up Prometheus steals fire from Zeus and the other gods gives it to humans heaven's prowess now mortal Zeus sticks it to Prometheus cause he knows knowledge knows how sharp its edge can be chains him to a rock an eagle eating his liver all day the liver regenerates every morning the eagle keeps eating keeps eating keeps eating with the patent for Oxycontin set to run out in 2013 Purdue Pharma reformulates it gets a new patent lobbies the old drug illegal no one steals from the gods no one dulls the blade of knowledge - That summer my first desk job insurance intakes at a doctor's office the relief of air conditioning pharma reps catering our lunches released from the fear of dropping a ladder on a foreman of threading my thumbnail with another drill bit the good doc scheduled in five minute increments I retyped patient addresses all hill towns sixty miles off the waiting room so full and grumpy I wondered about the etymology of patient but never what makes a person drive hours through the mountains wait hours for a flicker with the doc I was not paid to wonder I quit before I ever typed your name

different subject. The story of the serotonin hypothesis for depression, and its enthusiastic promotion by drug companies, is part of a wider process that has been called ‘disease-mongering’ or ‘medicalisation’, where diagnostic categories are widened, whole new diagnoses are invented, and normal variants of human experience are pathologised, so they can be treated with pills. One simple illustration of this is the recent spread of ‘checklists’ enabling the public to diagnose, or help diagnose, various medical conditions. In 2010, for example, the popular website WebMD launched a new test: ‘Rate your risk for depression: could you be depressed?’ It was funded by Eli Lilly, manufacturers of the antidepressant duloxetine, and this was duly declared on the page, though that doesn’t reduce the absurdity of what followed. The test consisted of ten questions, such as: ‘I feel sad or down most of the time’; ‘I feel tired almost every day’; ‘I have trouble concentrating’; ‘I feel worthless or hopeless’; ‘I find myself thinking a lot about dying’; and so on. If you answered ‘no’ to every single one of these questions – every single one – and then pressed ‘Submit’, the response was clear: ‘You may be at risk for major depression’.

In March, while people were dying at the rate of 10,000 patients a week, Dr. Fauci declared that hydroxychloroquine should only be used as part of a clinical trial.104 For the first time in American history, a government official was overruling the medical judgment of thousands of treating physicians, and ordering doctors to stop practicing medicine as they saw fit. Boldly and relentlessly, Dr. Fauci kept declaring that “The Overwhelming Evidence of Properly Conducted Randomized Clinical Trials Indicate No Therapeutic Efficacy of Hydroxychloroquine (HCQ).”105 Dr. Fauci failed to disclose that NONE of the trials he had used as the basis for that pronouncement involved medication given in the first five to seven days after onset of symptoms. Instead, all of those randomized controlled trials targeted patients who were already sick enough to be hospitalized.

McCullough points out that early treatment does not just prevent hospitalization; it quickly starves pandemics to death by stopping their spread. “Early treatment reduces the infectivity period from 14 days to about four days,” he explains. “It also allows someone to stay in the home so they don’t contaminate people outside the home. And then it has this remarkable effect in reducing the intensity and duration of symptoms so patients don’t get so short of breath, they don’t get into this panic where they feel they have to break containment and go to the hospital.” McCullough says that those hospital trips are tinder for pandemics, especially since, at that point, the patient is at the height of infectivity, with teeming viral loads. “Every hospitalization in America—and there’s been millions of them—has been a super-spreader event. Sick patients contaminate their loved ones, paramedics, Uber drivers, people in the clinic and offices. It becomes a total mess.” McCullough says that by treating COVID-19 at home, doctors actually can extinguish the pandemic.

Dr. Fauci, Bill Gates, and WHO financed a cadre of research mercenaries to concoct a series of nearly twenty studies—all employing fraudulent protocols deliberately designed to discredit HCQ as unsafe. Instead of using the standard treatment dose of 400 mg/day, the 17 WHO studies administered a borderline lethal daily dose starting with 2,400 mg.61 on Day 1, and using 800 mg/day thereafter. In a cynical, sinister, and literally homicidal crusade against HCQ, a team of BMGF operatives played a key role in devising and pushing through the exceptionally high dosing. They made sure that UK government “Recovery” trials on 1,000 elderly patients in over a dozen British, Welsh, Irish and Scottish hospitals, and the U.N. “Solidarity” study of 3,500 patients in 400 hospitals in 35 countries, as well as additional sites in 13 countries (the “REMAP-COVID” trial), all used those unprecedented and dangerous doses.62 This was a brassy enterprise to “prove” chloroquine dangerous, and sure enough, it proved that elderly patients can die from deadly overdoses. “The purpose seemed, very clearly, to poison the patients and blame the deaths on HCQ,” says Dr. Meryl Nass, a physician, medical historian, and biowarfare expert.

By March, front-line doctors around the world were spontaneously reporting miraculous results following early treatment with HCQ, and this prompted growing anxiety for Pharma. On March 13, a Michigan doctor and trader, Dr. James Todaro, M.D., tweeted his review of HCQ as an effective COVID treatment, including a link to a public Google doc.48,49 Google quietly scrubbed Dr. Todaro’s memo. This was six days before the President endorsed HCQ. Google apparently didn’t want users to think Todaro’s message was missing; rather, the Big Tech platform wanted the public to believe that Todaro’s memo never even existed. Google has a long history of suppressing information that challenges vaccine industry profits. Google’s parent company Alphabet owns several vaccine companies, including Verily, as well as Vaccitech, a company banking on flu, prostate cancer, and COVID vaccines.50,51 Google has lucrative partnerships with all the large vaccine manufacturers, including a $715 million partnership with GlaxoSmithKline.52 Verily also owns a business that tests for COVID infection.53 Google was not the only social media platform to ban content that contradicts the official HCQ narrative. Facebook, Pinterest, Instagram, YouTube, MailChimp, and virtually every other Big Tech platform began scrubbing information demonstrating HCQ’s efficacy, replacing it with industry propaganda generated by one of the Dr. Fauci/Gates-controlled public health agencies: HHS, NIH and WHO. When President Trump later suggested that Dr. Fauci was not being truthful about hydroxychloroquine, social media responded by removing his posts.

The raw data from CDC’s 1999 Verstraeten study showed that children who took thimerosal-containing hepatitis B vaccines in their first thirty days suffered an astonishing 1,135 percent higher rate of autism than children who did not.30 Verstraeten

The absurdity of expensive shots as a remedy for indigence, a salve for malnutrition, or the dearth of potable water is obvious when one considers that three billion people live on less than two dollars per day. Eight hundred and forty million people don’t have enough to eat. One billion lack clean water, or access to sanitation. One billion are illiterate. About a quarter of children in poor countries do not finish primary school.122 Poverty is a target-rich environment, but the data suggest that Gates’s vaccines miss the target altogether.

A 2017 CDC study links miscarriage to flu vaccines, particularly in the first trimester. Pregnant women vaccinated in the 2010/2011 and 2011/2012 flu seasons had two times greater odds of having a miscarriage within twenty-eight days of receiving the vaccine. In women who had received the H1N1 vaccine in the previous flu season, the odds of having a miscarriage within twenty-eight days were 7.7 times greater than in women who did not receive a flu shot during their pregnancy.

As Solomon discovered, the “volunteer” subjects of that unethical experiment were newborns aged three days or less.

Kids who refused too much, or threw up too much, they’d get a tube. First it was through the nose. But then it was more and more through the stomach. You’d see a certain child refusing over and over, and one day they’d come back from the hospital from surgery, and they had a tube coming right out of their stomach. If you asked why, the doctors said it was for “compliance

The researchers tracked every patient receiving fluvoxamine during the trial for 28 days and found about a 30-percent reduction in events among those receiving fluvoxamine compared to those who did not. Like almost all the other remedies, it is cheap and proven safe by long use. Fluvoxamine costs about $4 per 10-day course.

they could successfully treat high-risk COVID-19 patients as outpatients, within the first five to seven days of the onset of symptoms, with a chloroquine drug alone or with a “cocktail” consisting of hydroxychloroquine, zinc, and azithromycin (or doxycycline).

The raw data from CDC’s 1999 Verstraeten study showed that children who took thimerosal-containing hepatitis B vaccines in their first thirty days suffered an astonishing 1,135 percent higher rate of autism than children who did not.30 Verstraeten also documented a grim inventory of other neurological injuries including ADD/ADHD, speech and language delays, tics, and sleep disorders in children exposed to thimerosal. Verstraeten reported that these shocking signals prompted him to review, for the first time, the published medical literature, where he confirmed the alarming toxicity of mercury (thimerosal) to cause these injuries was biologically plausible.

Switzerland banned the use of HCQ; however, about 2 weeks into the ban, Switzerland’s death rates tripled, for about 15 days, until Switzerland reintroduced HCQ. COVID deaths then fell back to their baseline.

In his early AIDS days, Dr. Fauci had thrashed FDA as inhumane for demanding randomized double-blind placebo studies at the height of the pandemic. Now, here he was doing what he had condemned by blocking an effective treatment simply because it would compete with his expensive patent-protected pharmaceutical, remdesivir, and vaccines.

Remdesivir, it turned out, was hideously dangerous. Within 28 days, subjects taking remdesivir had lethal side effects including multiple organ failure, acute kidney failure, septic shock, and hypotension, and 54 percent of the remdesivir group died—the highest mortality rate among the four experimental drugs.

there have been 48,465 deaths among Medicare/Medicaid beneficiaries within fourteen days of a first or second dose of a COVID-19 vaccine.72,73 There are about 59.4 million Americans covered by Medicare, representing only 18.1 percent of the population, so these staggering numbers are roughly comparable to Steve Kirsch’s population-wide estimate of 150,000.

Dr. Fauci’s 2019 Ebola study proved that remdesivir, by day three, four, and five, caused acute kidney failure in upwards of 31 percent of patients. In less than five days of remdesivir treatment, 8 percent of all people died or experienced life-threatening multiple organ failure or kidney failure so severe they had to be taken off the drug. “So it may not be a coincidence that roughly the same number of hospitalized COVID patients—8–10x were dying in the first week,” says Cole. Dr. McCullough gives us a stark and clear summary: “Remdesivir has two problems. First, it doesn’t work. Second, it is toxic and it kills people.

Dr. Fauci, Bill Gates, and WHO financed a cadre of research mercenaries to concoct a series of nearly twenty studies—all employing fraudulent protocols deliberately designed to discredit HCQ as unsafe. Instead of using the standard treatment dose of 400 mg/day, the 17 WHO studies administered a borderline lethal daily dose starting with 2,400 mg.61 on Day 1, and using 800 mg/day thereafter. In a cynical, sinister, and literally homicidal crusade against HCQ, a team of BMGF operatives played a key role in devising and pushing through the exceptionally high dosing

AIDS activists and public health officials were wondering, “Where did all the grant money go? Did NIAID keep the money? Who benefited? Certainly not the tens of thousands of people with AIDS who grew angrier and angrier with each wasted, passing day.”19 Activists complained that Dr. Fauci was not being forthcoming about the status and enrollment of his clinical trials. He was stonewalling inquiries and had veiled the entire process in secrecy.

Meta-analysis co-authored by Julianne Holt-Lunstad, PhD, a professor of psychology and neuroscience at Brigham Young University, [found that] lack of social connection heightens health risks as much as smoking 15 cigarettes a day or having alcohol use disorder. [Holt-Lunstad] also found that social isolation is twice as harmful to physical and mental health as obesity. . . . “There is robust evidence that social isolation significantly increases risk for premature mortality, and the magnitude of the risk exceeds that of many leading health indicators.

Dr. Tess Lawrie: “This is what I don’t get, you know, because you’re not a clinician. You’re not seeing people dying every day. And this medicine prevents deaths by 80 percent. So 80 percent of those people who are dying today don’t need to die because there’s ivermectin.” Dr. Andrew Hill: “There are a lot, as I said, there are a lot of different opinions about this. As I say, some people simply. . . .

Dr. Tess Lawrie: “Fifteen thousand people a day times six weeks . . . Because at this rate, all other countries are getting ivermectin except the UK and the USA, because the UK and the USA and Europe are owned by the vaccine lobby.

On August 15, the FDA instructed, on its website: “You are not a horse.” In an August 21, 2021 Twitter post,84 the FDA expanded the theme: “You are not a horse. You are not a cow. Seriously, y’all. Stop it.” The White House and CNN also urged listeners that they should avoid veterinary products. CDC joined the chorus, warning Americans to not risk their health consuming a “horse de-wormer.” Elsewhere on its website, the CDC urged black and brown human immigrants to load up on ivermectin. “All Middle Eastern, Asian, North African, Latin American, and Caribbean refugees should receive presumptive therapy with: ivermectin, two doses 200 mcg/Kg orally once a day for two days before departure to the United States.85 Whether this was intended to deworm them or to prevent COVID transmission during travel to the US is unclear.

This is how we know that Anthony Fauci was well aware of remdesivir’s toxicity when he orchestrated its approval for COVID patients. NIAID sponsored that project. Dr. Fauci had another NIAID-incubated drug, ZMapp, in the same clinical trial, testing efficacy against Ebola alongside two experimental monoclonal antibody drugs. Researchers planned to administer all four drugs to Ebola patients across Africa over a period of four to eight months.10,11 However, six months into the Ebola study, the trial’s Safety Review Board suddenly pulled both remdesivir and ZMapp from the trial.12 Remdesivir, it turned out, was hideously dangerous. Within 28 days, subjects taking remdesivir had lethal side effects including multiple organ failure, acute kidney failure, septic shock, and hypotension, and 54 percent of the remdesivir group died—the highest mortality rate among the four experimental drugs.13 Anthony Fauci’s drug, ZMapp, ran up the second-highest body count at 44 percent. NIAID was the primary funder of this study, and its researchers published the bad news about remdesivir in the New England Journal of Medicine in December 2019.

The story, of course, was fraud. Days later, Oklahoma’s Sequoyah Northeastern Health System posted a categorical denial on its website, dismissing the entire story as mere fabrication. That Rolling Stone picture of the long lines was an Associated Press stock photo from the previous January, a photo of people waiting in line to get vaccines. As it turns out, not a single patient has been treated in Oklahoma for ivermectin overdose.

Following its pioneering world-record vaccine rollout, Gibraltar saw an immediate spike in deaths, suffering 2,853 fatalities per million inhabitants, a European per capita mortality record. During the first days of the rollout—which began with senior citizens—some 84 elderly died immediately after vaccination. Gibraltar’s shell-shocked Governor General said it was the largest mortalities ever suffered in the nation, exceeding even those endured during World War II.

In compliance with the WHO recommendation, Switzerland banned the use of HCQ; however, about 2 weeks into the ban, Switzerland’s death rates tripled, for about 15 days, until Switzerland reintroduced HCQ. COVID deaths then fell back to their baseline.118 Switzerland’s “natural experiment” had provided yet another potent argument for HCQ.

The report acknowledges that, “The BMGF developed a model of chloroquine penetration into tissues for malaria.”69 BMGF’s unique dosing model for the studies deliberately overestimated the amount of HCQ that necessary to achieve adequate lung tissue concentrations. The WHO report confesses that, “This model is however not validated.” Gates’s deadly deception allowed FDA to wrongly declare that HCQ would be ineffective at safe levels. The minutes of that March 13, 2020 meeting suggest that BMGF knew the proper drug dosing and the need for early administration. Yet their same researchers then participated in deliberately providing a potentially lethal dose, failing to dose by weight, missing the early window during which treatment was known to be effective, and giving the drug to subjects who were already critically ill with comorbidities that made it more likely they would not tolerate the high dose. The Solidarity trial design also departed from standard protocols by collecting no safety data: only whether the patient died, or how many days they were hospitalized. Researchers collected no information on in-hospital complications. This strategy shielded the WHO from gathering information that could pin adverse reactions on the dose.

The death rate climbed precipitously after the commercial introduction of AZT. In 1987, “AIDS” deaths rose by 46 percent with 16,469 people dying. In 1988, as more and more people received AZT, the death toll rose to 21,176, and then to 27,879 in 1989. Death rates rose to 31,694 in 1990, and 37,040 in 1991.110 At the end of the 1980s, HHS’s standard prescription for AZT was 1,500 mg a day. In 1988, the average survival time for patients taking AZT was four months.111 Even mainstream medicine couldn’t overlook the fact that the administration of higher doses led to much higher death rates.112 At the beginning of the 1990s, health officials lowered the daily dose to 500 mg. The average lifespan of AZT patients rose to twenty-four months in 1997, as deaths attributed to AIDS plummeted. Afterwards. CDC changed its counting metrics to make it difficult to count annual AIDS deaths.113

Forcing an entire population to accept an arbitrary and risky medical intervention is the most intrusive and demeaning action ever imposed by the United States Government, and perhaps any government. And it is based upon a lie. The Director of the CDC, Dr. Fauci, and the WHO have all had to reluctantly acknowledge that the vaccines cannot stop transmission. When Israel’s Director of Public Health addressed the FDA Advisory Panel, she left no doubt about the vaccines’ inability to stop transmission of the virus, or stop sickness, or stop death. Describing Israel’s situation as of September 17th, 2021, she said: Sixty percent of the people in severe and critical condition were, um, were immunized, doubly immunized, fully vaccinated. Forty-five percent of the people who died in this fourth wave were doubly vaccinated. Even so, three weeks later, on October 7th—just days before this book went to press—the President of the United States announced that he was ensuring healthcare workers are vaccinated, “because if you seek care at a healthcare facility, you should have the certainty that the people providing that care are protected from COVID and cannot spread it to you.” The President just told Americans that being vaccinated provides “certainty” that vaccinated people are “protected from COVID and cannot pass it to you.” Not one question was posed to the President about this stunning disconnect, about the obvious untruth—and that speech gives us a stark example of what’s going on. A televised image of an unchallenged leader mouthing untrue pronouncements to mislead and control the population—that is the world of George Orwell’s sadly prophetic novel, 1984. It

In September, Dr. McCullough used his own money to create a YouTube video showing four slides from his peer-reviewed American Medical Association articles to teach doctors the miraculous benefits of early treatment with HCQ and other remedies. His video went viral, with hundreds of thousands of downloads; YouTube pulled it two days later.

Similarly, a comprehensive 1977 study by McKinlay and McKinlay, formerly required reading in almost all American medical schools, found that all medical interventions, including vaccines, surgeries, and antibiotics, contributed only about 1 percent of the decline and at most 3.5 percent.17 Both CDC and the McKinlays attributed the disappearance of infectious disease mortalities not to doctors and health officials, but to improved nutrition and sanitation—the latter credited to strict regulation of food preparation, electric refrigerators, sewage treatment, and chlorinated water. The McKinlays joined Harvard’s iconic infectious disease pioneer, Edward Kass, in warning that a self-serving medical cartel would one day try to claim credit for these public health improvements as a pretense for imposing unwarranted medical interventions (e.g., vaccines) on the American public. As the McKinlays and Kass18 had predicted, vaccinologists successfully hijacked the astonishing success story—the dramatic 74 percent decline in infectious disease mortalities of the first half of the twentieth century—and deployed it to claim for themselves, and particularly for vaccines, a revered and sanctified—and scientifically undeserving—prestige beyond criticism, questioning, or debate.

Tweaking” is the jittery state which occurs after the drug is taken for many hours or days. Symptoms include euphoria, disturbed speech, agitation, anxiety, and sometimes paranoia with aggressiveness.

Freedom of Information documents obtained in January 2021 by the White Coat Waste project show that Dr. Fauci approved a $424,000 NIAID grant in 2020 for experiments in which dogs were bitten to death by flies.58 The insects carried a disease-carrying parasite that can affect humans. The researchers strapped capsules containing infected flies to the bare skin of twenty-eight healthy beagle puppies and kept them in agonizing suffering for 196 days before euthanizing them. NIAID acknowledged it subjected other animals, including mice, Mongolian gerbils, and rhesus monkeys to similar experiments.

If I was diagnosed with cancer, I would immediately start taking at least 50,000 IU of D3 per day and I recommend this to anyone else. There will be no Big Pharma study on high dose D3 for cancer as it is not patentable, and they cannot make any money from it.

So now Kadlec—who had, for twenty years, been writing scripts for using a pandemic to overthrow democracy and curtail constitutional rights—was in a perfect position to do just that. With this virus simulation, he included all the key players who would manage what was to become a de facto coup d’état sixty days hence.

Everyone was terrified of Fauci,” says Dr. Fishbein. “He runs the agency like a vindictive dictator. Everyone is frightened of him; everyone knows that you never cross Fauci.” In Farber’s words, “Fishbein became a ‘ghost.’ Nobody addressed him in the corridors, in the elevators, in the cafeteria. ‘There was an active campaign to humiliate me,’ he recalls. ‘It was as if I had AIDS in the early days. I was like Tom Hanks in Philadelphia. Nobody would come near me.

Pregnant women vaccinated in the 2010/2011 and 2011/2012 flu seasons had two times greater odds of having a miscarriage within twenty-eight days of receiving the vaccine. In women who had received the H1N1 vaccine in the previous flu season, the odds of having a miscarriage within twenty-eight days were 7.7 times greater than in women who did not receive a flu shot during their pregnancy.80

Similarly, a comprehensive 1977 study by McKinlay and McKinlay, formerly required reading in almost all American medical schools, found that all medical interventions, including vaccines, surgeries, and antibiotics, contributed only about 1 percent of the decline and at most 3.5 percent.17 Both CDC and the McKinlays attributed the disappearance of infectious disease mortalities not to doctors and health officials, but to improved nutrition and sanitation—the latter credited to strict regulation of food preparation, electric refrigerators, sewage treatment, and chlorinated water. The McKinlays joined Harvard’s iconic infectious disease pioneer, Edward Kass, in warning that a self-serving medical cartel would one day try to claim credit for these public health improvements as a pretense for imposing unwarranted medical interventions (e.g., vaccines) on the American public.

six days before the President endorsed HCQ. Google apparently didn’t want users to think Todaro’s message was missing; rather, the Big Tech platform wanted the public to believe that Todaro’s memo never even existed. Google has a long history of suppressing information that challenges vaccine industry profits. Google’s parent company Alphabet owns several vaccine companies, including Verily, as well as Vaccitech, a company banking on flu, prostate cancer, and COVID vaccines.50,51 Google has lucrative partnerships with all the large vaccine manufacturers, including a $715 million partnership with GlaxoSmithKline.52 Verily also owns a business that tests for COVID infection.53 Google was not the only social media platform to ban content that contradicts the official HCQ narrative. Facebook, Pinterest, Instagram, YouTube, MailChimp, and virtually every other Big Tech platform began scrubbing information demonstrating HCQ’s efficacy, replacing it with industry propaganda generated by one of the Dr. Fauci/Gates-controlled public health agencies: HHS, NIH and WHO. When President Trump later suggested that Dr. Fauci was not being truthful about hydroxychloroquine, social media responded by removing his posts.

If you're a CEO of Big Pharma who raises the price of a life-saving drug 600%, it's not competition you lack, it's a conscience. It's not poorly lit alleyways that are responsible for rape -- it's rapists. Let's address the real problem: CORPORATE GREED.

APPENDIX U: TREATMENT COST FOR INJECTABLE B12 Vitamin B12(hydroxocobalamin) 1,000 mcg/ml (30ml) vial costs approximately $36.00 per year for treatment 1,000 MCG = 1MG = 1ML INJECTED = $1.20 • Initial 7 injections daily or every other day then; • Maintenance: 1 ml IM or SC every 2 weeks = 24 ml per year or 0.5 ml SC every week = 24 ml per year • Syringes with needles (quantity 30): 1 ml syringe with 25 gauge needle costs 29 cents each or $8.70 per year (we recommend using 27 gauge needle) or insulin syringe with needle • 1 box of 100 insulin syringes with needles costs $28.56 and lasts over three years • Injectable hydroxocobalamin (1,000mcg/ml) is manufactured by Abraxis BioScience, Phoenix, AZ 85043, USA, and distributed by Watson Pharma, Inc.

Gibraltar Following its pioneering world-record vaccine rollout, Gibraltar saw an immediate spike in deaths, suffering 2,853 fatalities per million inhabitants, a European per capita mortality record. During the first days of the rollout—which began with senior citizens—some 84 elderly died immediately after vaccination. Gibraltar’s shell-shocked Governor General said it was the largest mortalities ever suffered in

Dr. Hill: “Well. . . .” Dr. Tess Lawrie: “This is what I don’t get, you know, because you’re not a clinician. You’re not seeing people dying every day. And this medicine prevents deaths by 80 percent. So 80 percent of those people who are dying today don’t need to die because there’s ivermectin.” Dr. Andrew Hill: “There are a lot, as I said, there are a lot of different opinions about this. As I say, some people simply. . .

Pediatric offices are receiving money from Big Pharma, insurance companies, and/or the government to promote vaccinations. (Chapter 3 and 4 – Solution #1). This is a blatant conflict of interest. This corruption has gone too far. If you decide you don’t want any vaccines for your child, or you decide to stop the vaccines due to a post vaccine reaction or illness you suspect may be due to the vaccines given, then the pediatric office may kick you out or turn you away from their practice. (Chapter 3 and 4 - Solution #2). This is unconscionable. But it is happening somewhere every day in our country. This is wrong. These offices should be there for their patients. They should not rule over us. Pediatric offices are businesses. As businesses, they should not be able to discriminate against people due to their personal beliefs and choices.

Burroughs Wellcome’s shares soared 45 percent on Dr. Fauci’s announcement, adding 1.4 billion pounds to the company’s UK stock market value in one day.86 The company’s CEO predicted that AZT profits would bring in over $2 billion per year.87 The PIs had handed NIAID its first successful drug trial. Dr. Fauci was now in the clear and he knew that the PIs had pulled his chestnuts from the fire. Not only had they given him a blockbuster

Accepts Healthy Volunteers.”38 As Solomon discovered, the “volunteer” subjects of that unethical experiment were newborns aged three days or less.39 NIAID randomized these infants to one of three doses of either experimental HIV vaccine or placebo.

Cause for Concern.” Produced by Meditel, the film described the material from the FOIA documents, exposed the crooked AZT trials as rank fraud, and chronicled the terrible toxicities of the drug. The next day, the charity, Wellcome Foundation, divested itself of most of its stock in Wellcome Pharmaceuticals, the parent company of Burroughs Wellcome, the manufacturer of AZT. Burroughs Wellcome stocks plunged, and the company suffered a series of hostile takeovers by SmithKline Beecham and then by Glaxo. Millions around the world viewed the UK documentary, but neither it nor any of the Medical AIDS-critical documentaries have ever been broadcast in the US.102 AZT is the most toxic drug ever approved for long-term use. Molecular biologist Professor Peter Duesberg has explained AZT’s mechanism of action: It is a random terminator of DNA synthesis, the life process itself.

Children’s bodies and brains are still in an early developmental stage of growth until at least the age of three. To inject infants with a variety of vaccines, which contain toxins and materials the body will recognize as foreign contaminants seems an ill-conceived “health” policy. Before the age of one, it is not recommended by our healthcare organizations to allow a child to eat honey, because a child’s system is not developed enough to handle “natures perfect food.” Currently, we are not only injecting infants with a plethora of vaccines in their first year but are starting them out with a vaccine on their first day on the planet. Is it any wonder why we have such rampant illness in the infant and adolescent population today? A little common sense appears to be needed here.

Up to 7% or more' of newborn infants are given antibiotics within the first three days after birth and almost all of them will receive a hep-B shot within the first day or two of life. This is a bad combination. To protect them from sepsis is understandable, but it is obviously overdone. This is another reason why hep-B vaccines should not be given routinely to all newborns. Toxins within the hep B vaccine plus antibiotics equals potentially adverse outcomes for these infants which can easily be avoided. After taking antibiotics yeast in the body can grow out of control, causing a variety of problems. Then to make things worse, we add more yeast into the infant’s body with the hep B vaccine, which contains brewer’s yeast. The combination of hep B vaccine and antibiotics directly after birth is not a good idea.

On January 27, 1988, NBC News broke the censorship blockade to broadcast the first of reporter Perry Peltz’s three-part exposé on the AZT Fischl trial.104,105 Peltz reported additional evidence of widespread tampering with the rules and the pervasive cheating, which she discovered had started on day one. Peltz learned

Dr. Fauci achieved that feat by allowing Merck to run Crixivan through a skeleton CRI process on a tiny cohort of ninety-seven volunteers in three groups, thereby winning the swiftest approval in history: forty-two days. That approval prompted open revolt by the AIDS community, which felt betrayed when Merck hiked up

Death by medication was normalized as an inherent part of progress.” All those poisoned Americans were just unfortunate casualties in Little Napoleon’s noble war against the germs.121 Dr. Fauci’s fraud persuaded hundreds of thousands of people to take AZT. For many of them, it was a lethal choice. In 1987, AZT became the AIDS “therapy” even though in the recommended dosage of 1,500 mg/day, it was absolutely fatal.122 Throughout the

the average lifespan of a patient on AZT was four years. The life expectancy only began to increase in 1990, when the FDA lowered the recommended dosages from 1,200 mg/day to 600.123 The quality of life on AZT was universally pretty miserable. Many credible scientists argued that AZT was killing more people than AIDS. Lauritsen estimated that AZT killed 330,000 gay men between 1987 and 2019.124 Many of the dead were perfectly

The drug had so many debilitating and lethal side effects that FDA, in an uncharacteristic act of civil disobedience against NIAID’s diminutive dictator, issued a black box warning. Nevertheless, desperate HIV-infected Americans rushed like doomed lemmings to take the drug. In 2010, FDA issued a statement that ddI can cause potentially a fatal liver disease called non-cirrhotic portal hypertension.126 Even with its demonstrated toxicity, Dr. Fauci used CRI parallel-track process to bypass the usual controls, to win approval for use of ddI in pregnant mothers who test positive for HIV. A 2019 study [Hleyhel et al., Environ Mol Mutagen (2019)127] found that ddI accounted for 16 percent of prescriptions for infected mothers and 30 percent of the cancers in their children. In 1996, Dr. Fauci used his expedited fast track to break another record by winning FDA approval for Merck’s HIV antiviral Crixivan; this time it took only six weeks.128 Dr. Fauci achieved that feat by allowing Merck to run Crixivan through a skeleton CRI process on a tiny cohort of ninety-seven volunteers in three groups, thereby winning the swiftest approval in history: forty-two days. That approval prompted open revolt by the AIDS community, which felt betrayed when Merck hiked up

would one day try to claim credit for these public health improvements as a pretense for imposing unwarranted medical interventions (e.g., vaccines) on the American public. As the McKinlays and Kass18 had predicted, vaccinologists successfully hijacked the astonishing success story—the dramatic 74 percent decline in infectious disease mortalities of the first half of the twentieth century—and deployed it to claim for themselves, and particularly for vaccines, a revered and sanctified—and scientifically undeserving—prestige beyond criticism, questioning, or debate. An Agency Without a Mission In 1955, as deaths from epidemic disease declined, NIAID’s forerunner organization at NIH, the National Microbiological Institute (NMI), became part of

suggests that over the summer, the vaccines killed nine times as many 15- to 19-year-olds as COVID did—eighty-one versus nine. “If not,” asks Jones, “what are the other possible explanations, and how likely are they?” Teen deaths among 15- to 19-year-olds have increased by 47 percent in the UK since they started getting the COVID-19 vaccine, according to official ONS data.101 Since the vaccine almost certainly causes more teen deaths and injuries than COVID-19, vaccinating this age group102 is highly unethical, and any physician who inoculates a healthy child is committing serious medical malpractice. Nevertheless, Anthony Fauci is urging that kids will be vaccinated in schools without parental consent, despite a mountain of evidence that the COVID-19 vaccines are killing American children and bestow on them no benefit. Media Censors Reports of Vaccine Deaths Most Americans are unaware of all this carnage because the mainstream and social media companies immediately scrub injuries reported by doctors, victims, and families. Media outlets like CNN and the New York Times ignore the tsunami of vaccine injuries and deaths while reflexively inflating those deaths they can blame on COVID. As part of a broad propaganda agenda, they report—with seeming glee—the occasional COVID death among the unvaccinated. Illustratively, on September 10, 2021, an ABC affiliate in Detroit solicited stories on its Facebook page about unvaccinated people who had died from COVID. Instead, the network got something they did not want: more than 230,000 messages containing heartbreaking stories of injuries and deaths from vaccines. None of these communications were reporting deaths among the unvaccinated. Readers shared the post over two hundred thousand times in ten days.103 Vaccinated Are Equally Likely to Spread COVID Dr. Fauci’s official theology makes “unvaccinated” America’s

CDC joined the chorus, warning Americans to not risk their health consuming a “horse de-wormer.” Elsewhere on its website, the CDC urged black and brown human immigrants to load up on ivermectin. “All Middle Eastern, Asian, North African, Latin American, and Caribbean refugees should receive presumptive therapy with: ivermectin, two doses 200 mcg/Kg orally once a day for two days before departure to the United States.85 Whether this was intended to deworm them or to prevent COVID transmission during travel to the US is unclear.

www dot mymedshop dot com dot au slash shop slash modafinil-200-m Modafinil 200 mg, known widely by its brand name Modalert, is a prescription medication that promotes wakefulness and mental alertness. It was originally developed to help people suffering from sleep disorders such as narcolepsy, obstructive sleep apnea, and shift work sleep disorder. Over time, Modalert has also become popular among professionals, students, and individuals who want to improve focus, memory, and productivity. It is considered one of the most effective nootropic or “smart drug” options available today. What Is Modafinil 200 mg (Modalert) Modalert 200 mg contains Modafinil as the active ingredient. It is a central nervous system stimulant that affects certain natural chemicals in the brain to promote alertness. Manufactured by Sun Pharma, Modafinil 200 mg, one of India’s leading pharmaceutical companies, Modalert is trusted globally for its quality and effectiveness. Each tablet delivers 200 milligrams of Modafinil, which is considered a standard and powerful dose for most adults. How Modafinil 200 mg Works Modafinil works by altering the natural neurotransmitters in the brain responsible for regulating sleep and wakefulness. It primarily increases dopamine levels by blocking its reuptake, allowing for a longer-lasting feeling of alertness. Additionally, Modafinil influences the levels of histamine, norepinephrine,Modafinil 200 mg, and orexin in the brain, all of which are linked to energy, concentration, and mood. Unlike traditional stimulants such as amphetamines, Modafinil does not cause hyperactivity or restlessness. Instead, it promotes a smooth and focused state of wakefulness that helps users remain productive for longer periods without feeling overstimulated. Medical Uses of Modafinil 200 mg (Modalert) Modafinil 200 mg is primarily prescribed for treating medical conditions that cause excessive daytime sleepiness. People with narcolepsy benefit from this medication as it helps them stay awake and alert during the day. In the case of obstructive sleep apnea, even after using breathing devices, many patients continue to feel fatigued. Modafinil helps in reducing this residual sleepiness and restores normal daytime activity. For individuals working in night shifts or irregular hours, Modafinil helps maintain alertness during working hours and supports better cognitive performance. These medical applications make Modalert an essential part of sleep disorder management. Off-Label Cognitive Benefits Apart from its medical applications, Modalert 200 mg is widely known for its off-label use as a cognitive enhancer. Many students and professionals use it to increase focus, attention, and productivity. It is especially Modafinil 200 mg, favored by individuals who have to work long hours or manage demanding tasks that require mental endurance. Modafinil enhances the ability to concentrate, retain information, and make decisions efficiently. Users often report experiencing a sense of mental clarity, motivation, and calm alertness that allows them to perform at their best for extended periods. Dosage and Administration The usual recommended dosage of Modafinil is 200 mg once a day. For people taking it to manage narcolepsy or sleep apnea, the tablet is best taken in the morning. Those using it for shift work sleep disorder are advised to take the tablet about one hour before starting their work shift. When used for focus and productivity, it is best taken early in the day to prevent interference with nighttime sleep. The medication can be taken with or without food, but it should be swallowed with water. Modafinil should not be taken late in the day, as it may cause insomnia due to its long-lasting effects. Duration and Effectiveness

It takes a village to raise a child” has grievously overstepped its boundaries. I’d like to think this phrase was correct and valuable back when cultural norms were prevalent, generally everyone agreed on right and wrong, and evil was a bit more closeted. Now, the days are so dark and evil; gender and sexuality have worked their way into tiny children’s classrooms, vaccines by Big Pharma are being marketed heavily at doctors’ offices, media is divisive and deceitful, technology attempts to corrupt the youngest among us with porn exposure younger than ever before, and sex offenders lurk everywhere. I do not want the village raising my child.