If you took a Wuhan coronavirus (Covid-19) “vaccine,” the American Red Cross will not accept blood plasma donations from you due to the inherent toxicity issues caused by the injection.
As it turns out, convalescent plasma should only be collected from the unvaccinated who still have clean blood that has not been contaminated with deadly spike proteins and other chemicals that threaten to kill those who receive blood transfusions.
Thanks to “Operation Warp Speed,” there is now a massive shortage of pure blood in the United States that has not been tainted with genetic modifications and other damage. Mass vaccination, in other words, is effectively killing people who desperately need unvaccinated blood but cannot find it.
A now-archived document from the American Red Cross explains that anyone who takes “any type of COVID vaccine” is “not eligible to donate convalescent plasma” because of the serious risks involved.
“One of the Red Cross requirements for plasma from routine blood and platelet donations that test positive for high-levels of antibodies to be used as convalescent plasma is that it must be from a donor that has not received a COVID-19 vaccine,” the document explains.
Scientifically speaking, it is critical for those receiving donor blood to have sufficient antibodies directly related to their own immune systems. Tainted blood from vaccinated people does not qualify.
“This is to ensure that antibodies collected from donors have sufficient antibodies directly related to their immune response to a COVID-19 infection and not just the vaccine, as antibodies from an infection and antibodies from a vaccine are not the same.”
Red Cross discontinues convalescent plasma donation program entirely after FDA rule change
CDMedia has been approached by a group of parents terrified about what is happening to their children at the United States Military Academy at West Point.
Cadets are being threatened with solitary confinement, separation from the Academy, essential training is being refused, and they are facing daily direct pressure from senior officers at the institution if they do not take the Covid-19 mRNA vaccine.
The Covid-19 vaccines are experimental and no one can be forced to take them. They are voluntary per the Center for Disease Control and the Food and Drug Administration.
Apparently, this means nothing to West Point officials who are essentially forcing cadets to take these experimental drugs or be expelled.
Over 700 cadets initially refused to vaccinate but that number has now dwindled to below 100. Direct pressure by senior officials at the institution is ramping up daily.
Parents of these remaining holdouts are terrified and are hiring legal counsel, banding together to fight this perceived criminal behavior by those in power over their children.
Pressure is being applied in spite of the fact that information is now being released the vaccines have caused at least 4,400 deaths in the U.S, and numerous medical problems including blood clots. Dr. Anthony Fauci has been caught repeatedly lying about Covid-19, as well as mask mandates. CDMedia will be reporting more on this in a follow-on article shortly.
Cadets have been told the FDA is not moving fast enough to approve the vaccine but officials are pressuring cadets anyway, saying the U.S. Army may move to force all to vaccinate.
Those that were not vaccinated are forced to wear masks, which medically and publicly mark them in the Corps of Cadets which is against HIPAA. This is another form of pressure.
Evidence has shown that young people have almost zero chance from dying of Covid, and rarely have severe reactions to the man-made disease.
Dr. McCullough Sounds The Alarm On Covid Jabs: All Covid-19 Vaccines Produce The Dangerous Wuhan Spike Protein (AUDIO)
Fuellmich and his team present the incorrect PCR test and the order for doctors to describe any comorbidity death as a Covid death – as fraud.
The PCR test was never designed to detect pathogens and is 100% inaccurate at 35 cycles. All PCR tests monitored by the CDC are set at 37 to 45 cycles. The CDC acknowledges that tests over 28 cycles are not allowed for a positive reliable result.
This invalidates over 90% of the alleged Covid cases / “infections” detected by the use of this incorrect test.
In addition to the incorrect tests and fraudulent death certificates, the “experimental” vaccine itself violates Article 32 of the Geneva Convention.
Under Article 32 of the 1949 Geneva Convention, “mutilation and medical or scientific experiments not required for the medical treatment of a protected person” are prohibited.
According to Article 147, conducting biological experiments on protected persons is a serious breach of the Convention.
The “experimental” vaccine violates all 10 Nuremberg codes – which carry the death penalty for those who try to break these international laws. More
Statements in this site are substantiated with facts that will stand in a court of law. Informed Consent requires a flow of information. Click on the hyperlinked sections to direct you to primary sources such as CDC, WHO, FDA documents.
Anyone trying to take down this site will be named as codefendant in Nuremberg 2.0 for being an accomplice to crimes against humanity. That includes social media. Lawyers are standing by.
***
Did you know?
1. The FDA did not approve Moderna or Pfizer mRNA gene therapeutics they dubbed “vaccines”. It simply authorized them. Fauci confirms.
19 doctors warned the world of the dangers. AstraZeneca is being dropped by 24 countries.
The CDC also confirms(2) the Pfizer & Moderna jabs are the deadliest of all “vaccines”, also in a bar chart. 5 prominent doctors discuss how the Covid jab is a bioweapon.
March 3, 2021 (Children’s Health Defense) — On Friday, the U.S. Food and Drug Administration (FDA) granted Emergency Use Authorization for Johnson & Johnson’s (J&J) COVID vaccine, paving the way for the one-shot vaccine to be administered beginning this week.
The Centers for Disease Control and Prevention (CDC) also recommended the vaccine for people 18 and older. On Sunday, J&J revealed plans to test its one-shot vaccine on infants, including newborns, pregnant women and the immunocompromised. The expanded clinical trials were laid out in the company’s application for emergency use approval and in briefing materials provided to the FDA and discussed briefly during the meeting.
According to the New York Times, the plan for expanded clinical trials met the approval of Dr. Ofer Levy, director of the Precision Vaccines Program at Harvard’s Boston Children’s Hospital and a member of the FDA’s advisory committee that reviewed the company’s vaccine data.
When Levy saw the outlines of the planned trials, he said: “They did not get into a lot of detail about it but did make it clear they will be pursuing pediatric and maternal coronavirus immunization studies.”
A spokesperson for Janssen Biotech, a J&J subsidiary, confirmed the company plans to extend clinical trials to children –– first to children between the ages of 12 and 18, and immediately after to newborns and adolescents, then to pregnant women and immunocompromised individuals. Continue reading here
“The party line recommends doing nothing for symptoms of fever, coughing, or breathing problems other than rest, stay home, drink fluids, and monitor. The threshold for calling the doctor is appalling: coughing up blood, trouble breathing, chest pain, confusion, severe drowsiness, or “a blue tint to your lips or face.” Wait until you turn blue?!”
Election irregularities, Chinese spies seducing a congressman, and the shocking revelation that “Dr.” Jill Biden was not a real doctor briefly let us turn our attention away from COVID-19. Unfortunately, COVID is still here and has made it to Antarctica. COVID continues to directly or indirectly hasten deaths. Along with the arrival of two much anticipated vaccines is a new active variant. The effects of both remain to be seen.
For months we’ve heard that COVID is not like the flu. It is a different animal. It may leave the infected person with long term aftereffects. Given the potential problems, the FDA, CDC, NIH, HHS and the alphabet health agencies should be advocating for early pharmacological treatment and prevention. Instead, we are told to wash our hands, wear masks—which may or may not help—and to stay away from one another. Indeed, as California’s Health and Human Services Secretary admitted, the state’s order banning outdoor dining and closing playgrounds was “not a comment on the relative safety” of the activity but a tactic for keeping people at home.
Stay home although 66 percent of new coronavirus hospitalizations in New York were in people who had not routinely left their homes. Stay inside although there are studies echoing observations during the 1918 flu pandemic finding that people who went outside had better outcomes. A recent Spanish study showed that 80 percent of patients with COVID had low levels of vitamin D. Another study found that people with adequate vitamin D levels had a 51 percent lower risk of dying from COVID. People at risk for vitamin D deficiency include those who have dark skin, are elderly or overweight, or stay indoors. Interestingly, these groups are particularly hit hard by COVID. More
Here is why my respect for the nighttime talk show hosts (ex Stephen Colbert, who is a comedic genius, in my opinion) has plummeted, mainly because of their blind obedience to conform to their TV Network’s Big Pharma/Big Vaccine corporate conflicts of interest. See the facts at the very end of this emailing.
Anyone up for boycotting the Mainstream Media/TV/Radio (even including PBS and NPR) entities that are so subservient to the Big Pharma/Big Vaccine/Big Corporations – at least until they do their Mea Culpas over promoting the whole COVID/Lock-down mess? GGK
Subject: VIP: Three short videos, Exposing the high iatrogenic death rates related to the ICU conditions in New York City hospitals, etc
1] First watch this Nurse Practitioner report on the high iatrogenic death rates related to the horrific ICU conditions in New York City hospitals, particularly from aggressive ventilator over-use and fear-based medical “caregiver” distancing between staff and patient.:
As I watched this I remembered noting something on TV recently about the thousands of fast-tracked Ventilators that are being manufactured and sent to hospitals everywhere, most of which will likely never be used. I doubt that any television program will ever do an expose about the thousands of panic-produced ventilators that were ordered because of the hysteria coming from the CDC, NIH, HIAID, FDA, Bill Gates Foundation, Mainstream Media, etc.
2] Then watch the following two short videos that also concern the COVID hysteria: More
The Alleged Coronavirus “Plague” and the Unnecessary Risking of a Second Great Depression – Thanks to Big Pharma, The Globalist/Corporate Oligarchs and Kissinger’s Eugenics Movement
1] Why Anything that the Financially-compromised CDC says About Anything, Especially the Current Coronavirus “Pandemic”, Must be Taken With a Giant Grain of Salt
(That is, as long as the agency denies its decades of serious conflicts of interest and also continues to be subservient to the nefarious, hidden economic interests of Big Pharma Corporations like Roche and Regeneron and Billionaire Wall Street Oligarchs like Bill Gates)
The Centers for Disease Control and Prevention (CDC) includes the following disclaimer with its recommendations: “CDC, our planners, and our content experts wish to disclose they have no financial interests or other relationships with the manufacturers of commercial products… The CDC does not accept commercial support.”More
As many people are coming to realize, you have put yourself in a compromising position just by going to your doctor. Your health is the last thing on their minds in too many cases. On one hand claiming not to know about the adverse and at times deadly effects of vaccines and medications, the alternative is that they do know, but don’t care. Many people have found themselves faced with a doctor whose ego is bigger than the room they sit in. Arrogantly obnoxious in many cases, they make it clear that being questioned about therapies is far beneath them. How dare you?
Our healthcare is supposed to be a partnership between doctor and patient. Instead it has become a system of tyranny; the doctor obviously perturbed that he/she actually had to see you, and even more so that you might dare to express your thoughts about what crap they are planning for you.
The movement of the public away from pharmaceuticals and vaccines and towards natural medicines is growing by the day. In response to this, the CDC, FDA and their partnering pharmaceutical corporations are racing to outlaw and neutralize this movement. Ignoring the massive numbers of deaths each year due to medications and vaccines, every effort is made to render alternative natural treatments unavailable.
Many physicians have less knowledge than their patients do concerning deadly medications and vaccines. We routinely see TV advertisements for medications that include the possible side effects, one of which is death. Why would any doctor prescribe medications that could cause the death of the individual? Even when patients attempt to report adverse effects, they are mocked and marginalized by their doctor. Rarely do they ever report these adverse symptoms to the CDC. The CDC claims they only receive an estimated 1% of all actual side effects, including death, as a result of the medications and vaccines. But your doctor will emphatically deny the adverse conditions you are reporting to them , instead claiming it is unrelated. Never mind that you didn’t have these symptoms before, you are just petulantly complaining.
Too many are still recommending chemotherapy and radiation after a diagnosis of cancer. Both therapies known now to cause more premature deaths than the cancer itself. It would appear that many of them are more concerned with kickbacks, payoffs and other perks offered by pharmaceutical sales people, and too many will happily prescribe medications and vaccines, the side effects of which cause lifelong illness and the onset of disease. They don’t care. Or so it would seem.
Elderly people appear to be a targeted group for medical exploitation. Of course there are major opportunities for up-coding, surprise billing, and outright fraudulent charges that have been the catalyst for the scamming of 30-60 billion annually in Medicare costs attributable to medical providers. It isn’t the elderly who collect billions of dollars annually from Medicare….it’s those holier than thou medical providers. There isn’t an elderly individual anywhere in the country who can bill, or collect, funds from Medicare.
Long gone are the days when the family doctor was a trusted friend and partner in your family’s healthcare. Those doctors have been replaced by self absorbed, ego driven, white coated demi-gods who are far more concerned with being adored and feared than they ever could be with your health.
The U.S. Food and Drug Administration (FDA) has published shocking results which found that cells used in the manufacturing of numerous childhood vaccines are often contaminated with serious viruses including cancer.
The FDA study looked at vaccines that are made from living cells, or replicated cell substrates that some manufacturers are investigating to create. According to research, these cells are oftentimes contaminated with hidden viral fragments which have the potential to cause cancer.
These viruses are dormant, meaning they live “quietly” inside other cells. However, eventually these cells no longer hide and circulate throughout the body in the form of serious disease. As a result, a person injected with a vaccine containing these cancer-causing micro-organisms may not display signs of health complications until long after they have been jabbed sometimes several years later.
An experiment injecting rodents with vaccines yielded surprising results showing that the rats now had tumor cells.
“In some cases the cell lines that are used might be tumorigenic, that is, they form tumors when injected into rodents,” the FDA paper explains.
“Some of these tumor-forming cell lines may contain cancer-causing viruses that are not actively reproducing. Such viruses are hard to detect using standard methods. These latent, or ‘quiet,’ viruses pose a potential threat, since they might become active under vaccine manufacturing conditions.
“US military casualties of war,” the grand total of all military deaths in the history of this country, starting with the Revolutionary War, is 1,312,612.
In any given 10 years of modern medical treatment? 2,250,000 deaths (Starfield).
Sociopathic, For-profit Corporations Own Healthcare in America
Ever since my fellow classmates and I took the Hippocratic Oath when we graduated from the University of Minnesota medical school in 1968, most of us (now retired for a decade or more) tried to fulfill our duties as physician-healers while also trying to not harm our patients in the process.
But times have changed since the Reagan years, when legislation was passed (in 1986) that made it illegal for parents whose children were killed or wounded by vaccines to sue the guilty pharmaceutical corporations (or the physicians or clinics that ordered the injections of the toxic substances, which the US Supreme Court later acknowledged were “inherently unsafe”). (Read about the National Childhood Vaccine Injury Act of 1986 at: https://www.nvic.org/injury…/nvic-position-on-1986-childhood-vaccine-injury-act.as…)
The crass, for-profit multi-national pharmaceutical corporations that have taken over medicine during the second half of my medical career have made it difficult for ethical physicians (and nurses) to honor their Hippocratic Oaths and to do the healing that they were trained to perform.
The interference by healthcare-related corporate powers in the practice of ethical and compassionate care is likely a major reason for the high rate of physician suicides and the fact that more and more physicians are wanting to quit the practice of medicine.
This column is also another attempts at explaining why the infant mortality rate among American infants is the highest in the world (among the 24 most economically-advanced nations) while American infants are also the most over-vaccinated in the world! (Please study the CDC’s-recommended chart of childhood vaccines in the archived version of this column.) What other interpretation could logically be applied to that reality? More
Across the country, frenzied legislators are responding to the pharmaceutical industry’s orchestrated fear campaign around measles by seeking to impose further mandating of Merck’s measles, mumps and rubella (MMR) vaccine. Although ongoing mumps outbreaks involving thousands of at-risk adolescents and young adults completely dwarf the number of measles cases, no one is covering the mumps story—because it will expose the fact that Merck has been in court for over eight years due to scientists blowing the whistle on Merck’s fabrication and falsification of the effectiveness of the mumps component of its MMR vaccine. Instead of punishing Merck for its chicanery, legislatures are rewarding the company by making it impossible to refuse Merck’s profitable vaccine, subjecting a generation of American children to the risk of serious complications from mumps infection at an age that nature never intended.
When younger children experience mumps, the virus is relatively harmless; infected children often exhibit no symptoms. When mumps strikes adolescents or adults, on the other hand, the infection can cause far more serious adverse effects, including inflammation of various organs (brain, pancreas, ovaries and testicles)—as well as damage to male fertility.
Inflammation of one or both testicles (a condition called orchitis) occurs in approximately one in three post-pubertal men who get mumps and can contribute to sperm defects and subfertility as well as impairing the function of cells that produce testosterone. An estimated 30% to 87% of men with bilateral orchitis induced by mumps experience full-blown infertility—a major cause for concern given the significant declines in male fertility observed over the past several decades. Thus, it appears that Merck’s vaccine, instead of protecting children, not only delays onset of disease to later age cohorts but has the potential to cause serious and permanent injury.
Merck and mumps vaccines
Let’s look at a quick history of mumps and MMR vaccination in the United States. The Food and Drug Administration (FDA) licensed Merck’s initial mumps-only vaccine in 1967. In 1971, Merck introduced its first combination MMR vaccine, followed by the MMR-II vaccine in 1978 (which repurposed the rubella component) and the MMR-plus-varicella (MMRV) ProQuad vaccine in 2005. Since the initial 1967 vaccine, Merck has enjoyed a unique monopoly position in the U.S. market for mumps and MMR vaccines, with combined sales of MMR-II and ProQuad bringing in over $720 million in 2014 alone. Merck consistently places in the top five pharmaceutical companies globally, and the market valued its stocks at a seven-year high as of late 2018. More
Recently we told you about a statement made by Commissioner Scott Gottlieb (who has since resigned his post) concerning the FDA’s regulatory approach to dietary supplements. The statement was short on details but gave us cause for concern. Now it appears as if those fears were warranted: the FDA is attempting to create a mandatory list of all supplement products in the US. Such a list could be used to target certain supplements and remove them from store shelves, and we must oppose it.
This revelation comes as a result of the FDA’s release of its 2020 budget estimates. In that document, the FDA requests the authority to “strengthen” its implementation and enforcement of the Dietary Supplement Health and Education Act (DSHEA) by requiring each supplement manufacturer to register all the products it makes, including all the ingredients of those products, with the agency. Note that an act of Congress would be necessary to grant the FDA the authority to create such a list.
This is one of the greatest attacks on the public since the creation of TSA. This is a direct assault on individual rights. No one in this hearing is mentioning that almost all recent outbreaks of measles, mumps and “flu” are in the 90% or above fully vaccinated. At this point in the hearing, unvaccinated children are being represented as a threat to children who might be immuno-compromised. The exact opposite is true. Children who have been vaccinated within 2-3 weeks prior to exposure are actively shedding the various viruses they have been intentionally infected with via the vaccines. READ THE INSERTS! The inserts state plainly that you are actively spreading the viruses from the vaccines!
Things are really heating up out there. With social media platforms like Pinterest de-platforming organizations like ours critical of vaccine policy and safety, Amazon pulling vaccine documentaries like VAXXED, 100 bills in 30 states aimed at stripping vaccine exemptions, and the FDA commissioner indicating that if state legislators don’t abolish vaccine exemptions federal agencies may step in, the stakes have never been higher when it comes to whether Americans will take action or stand by while our basic health freedoms are permanently removed.
Today’s Congressional hearing at 10:00 am, EST (link to watch here) will feature unilaterally pro-vaccine witnesses in what will likely be pure political theater. There will be no discussion of the over $4 billion dollars paid out by the government to vaccine injured families, nor the fact that not a single vaccine in today’s CDC immunization schedule was validated as safe and effective through a true, saline placebo-controlled clinical trial, much less studied for the dozens added together. In the articles below, you will find impassioned and rational discussion about the implications of this country-wide race into medical fascism and what you can still do about it — before its too late.
Please support independent platforms like GreenMedInfo which are poised to be removed from major social media platforms simply for asking questions and referencing peer-reviewed, published research that challenges the official narrative of health organizations like the CDC, FDA, and WHO who are increasingly behaving like wholly owned subsidiaries of the very multinational corporations they are charged with regulating, or at least informing them with the unbiased facts.
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Here’s how it usually goes: You say you have some doubts about vaccine safety and all those vaccinations the government requires you to give your kids. You say you’re concerned about serious side-effects you keep reading about, and particularly potential links to autism and autoimmune disorders, and the reports of encephalitis and shock. A typical response from mainstream proponents of vaccines would proceed like this…
“Oh, you’re being silly, you don’t know the science. Look, 99.9% of all doctors and scientists will tell you that vaccines are safe and effective. The science is solid, it’s long been proven beyond a shadow of a doubt.”
Ninety-nine point nine percent. That sounds pretty convincing. Of course, it’s unclear what formula, study or survey was used to come up with that figure, so you start to do your own research, and you quickly realize there are lots of doctors and scientists, in addition to well informed parents, journalists and consumer advocates, who do not subscribe to the establishment’s mantra about vaccine safety and effectiveness. They do not believe the myth that the science is settled, and some are very vocal about their reservations or opposition to it.
The more you read, the more you start to realize that there is a growing chorus of doctors, scientists, nurses, and other health care providers who have serious questions about the current vaccine paradigm favored by the pharmaceutical industry, government agencies (such as the Centers for Disease Control and Prevention [CDC] and Food and Drug Administration [FDA]), medical trade groups (such as the American Academy of Pediatrics [AAP], the American Medical Association [AMA], the American Academy of Family Practice [AAFP], etc, etc, and the mainstream media (which relies on Big Pharma’s advertising income that represents 70 % of annual revenues). More
These are my sentiments along with a double major middle finger salute to the Medical Mafia, Pig Pharma, Lying Vaccine industry, FDA (Fraud & Death Administration) , CDC (Center for Disease Continuation), Lamestream media, politicians, government & all their subsidiary’s!
Only fools trust these criminal organizations.
CHECK OUT THE MANY, MANY, MANY LINKS BELOW OF FRAUD & DECEPTION.
Total corruption: Drug companies bought their way onto FDA advisory panels
It is now an undeniable fact that the pharmaceutical industry weaseled its way onto key U.S. Food and Drug Administration (FDA) advisory panels, which were instrumental in shaping the way drugs are safety tested and approved. According to The Washington Post (WP), a recent public records request has revealed that drug companies purchased special access onto these panels, where they were given the keys to the kingdom in swaying decision-makers about official drug policy. http://www.naturalnews.com/042562_total_corruption_drug_com…
The FDA continues to be one of the most dangerous government agencies in the United States. The sheer scope of people it affects with its corruption is staggering.
The ultimate guide to vaccine information, anti-pharma news, and more
06/07/2018
FINALLY — Comprehensive, authoritative information about vaccine exemptions you can trust, from Alan Phillips, J.D., a leading vaccine rights attorney with years of experience helping clients throughout the U.S. legally avoid vaccines in a wide variety of vaccine-refusal settings. Recommended By Dr. Tenpenny
The HPV vaccine continues to be one of the most controversial vaccines in history. Numerously reported side-effects stemming from the Gardasil shot have caused parents worldwide to clamor at the thought of giving it to their teenage children. New Jersey, in fact, is attempting to make the HPV vaccine mandatory, which tells you just about everything you need to know about how parents likely feel over the matter.
In 2018 already, there have been 85,329 reports of adverse reactions to the HPV vaccine, as reported by the VigiAccess database.
Now, Merck is being accused of “fast-tracking” the Gardasil vaccine, according to GreenMedInfo.
Back in 2016, a California family filed a complaint with the Superior Court of the State of California against Gardasil maker, Merck. They claim that their daughter received the Gardasil shot three times over the course of a year starting in 2010. The girl, over the next few years, would be diagnosed with POTS and later on, a small fiber neuropathy that affected her entire body.
Her family became convinced that their daughter’s health issues stemmed from the Gardasil shots she took in the years prior. The family has accused Merck of deceitful marketing practices and rushing the drug to market.
Media won’t investigate medically-caused death numbers
by Jon Rappoport
May 16, 2018
Imagine a Congressional hearing held before media cameras, with reporters all over the US and Europe ready with shocking articles about one of the leading causes of death—
SENATOR: Sir, I have the numbers in front of me. How can you keep this secret from the public?
FDA COMMISSIONER: It’s not a secret, sir. Many experts know about it.
SENATOR: I’m looking through the trillion-dollar federal budget. I’m looking for the money allocated to fix this horrible situation. Where are those funds?
FDA COMMISSIONER: Nowhere.
I know major media won’t investigate medically-caused death numbers, because I’ve published reports for years, and I’ve contacted news people with the facts; and nothing happens.
So we begin with a few citations.
July 26, 2000, Journal of the American Medical Association; author, Dr. Barbara Starfield, revered public health expert at the Johns Hopkins School of Public Health; “Is US health really the best in the world?”
(A Few Facts That Essentia’s Policy-makers Should Have Considered Before Deciding to Force Their Employees to Submit to Flu Vaccinations Without Obtaining Their Fully Informed Consent)
“The CDC says that 36,000 people die from the flu every year in the US. But actually, it’s closer to 20. However, we can’t admit that, because if we did, we’d be exposing our gigantic psyop. The whole campaign to scare people into getting a flu shot would have about the same effect as warning people to carry iron umbrellas, in case toasters fall out of upper-story windows…and, by the way, we’d all be put in prison for fraud.” – Jon Rappoport More
A Collection of Recent Journal Articles Solidifying the Connections Between America’s Over-Vaccination Agenda and the Epidemics of Autism Spectrum Disorder and Chronic Autoimmune Disorders
“It is a near certainty that the AMA, the AAP, the IOM – and the recent critics of this column’s statements of scientific fact regarding the many dangers of the neurotoxicity of America’s over-vaccination programs – have little or no knowledge of the following research studies that totally debunk their claims that all vaccines are both safe and effective and that Big Medicine and Big Pharma can be trusted to implement their over-vaccination agendas, even to the point of forcibly vaccinating people against their wills.”
In an obscure interview back in 1956, the entertainer Elvis Presley was quoted as saying: “Don’t criticize what you don’t understand, son. You never walked in that man’s shoes.” But But none of Elvis’s many song-writers ever wrote a song that included that wonderful truism.
However, Bob Dylan, in his iconic “The Times They Are A-Changing” (1962), immortalized the phrase. It is not likely that Dylan stole the phrase from one of Presley’s songs because Elvis once admitted: “I’ve never written a song in my life.”
Dylan’s poetic truism has always stayed with me. To remind readers of its power, here is the fourth verse of that song:
“Come mothers and fathers
Throughout the land And don’t criticize
What you can’t understand
Your sons and your daughters
Are beyond your command
Your old road is rapidly agin’
Please get out of the new one if you can’t lend your hand
For the times they are a-changin’.
There is a surge of anti-intellectualism and anti-science belief systems in the United States. People who know nothing about climate science are ridiculing altruistic climate scientists who know what they are talking about. Respected, unbiased scientists (those who are not in the back pockets of the fossil fuel and coal industries) are fulfilling their moral duty to warn the rest of us about the imminent danger of potentially unstoppable – and catastrophic – warming of the planet, a reality that could easily make the planet unlivable for animal life n the near future (like the gradually expanding Sahara Desert has been exhibiting for us for years).
Unbiased geological scientists, scholars and assorted well-informed citizen activists (at least those who have not been hired and thus co-opted by Big Mining) understand the potentially catastrophic dangers of sulfide mining that is threatening my home state of Minnesota. These altruistic scientists and citizen activists are being viciously demonized (even with death threats) by some folks who happen to live in the boom-and-bust (non-sulfide) iron ore country that now has commercially-viable copper sulfide ore deposits in the water-rich part of the state. More
“The desire to take medicine is perhaps the greatest feature which distinguishes man from animals.” — Sir William Osler
“More than 50 conditions can cause or mimic the symptoms of dementia.” and“Alzheimer’s (can only be) distinguished from other dementias at autopsy.” — from a Harvard University Health Publication entitled What’s Causing Your Memory Loss? It Isn’t Necessarily Alzheimer’s
“Medications have now emerged as a major cause of mitochondrial damage, which may explain many adverse effects. All classes of psychotropic drugs have been documented to damage mitochondria, as have statin medications, analgesics such as acetaminophen, and many others…Damage to mitochondria is now understood to play a role in the pathogenesis of a wide range of seemingly unrelated disorders such as schizophrenia, bipolar disease, dementia, Alzheimer’s disease, epilepsy, migraine headaches, strokes, neuropathic pain, Parkinson’s disease, ataxia, transient ischemic attack, cardiomyopathy, coronary artery disease, chronic fatigue syndrome, fibromyalgia, retinitis pigmentosa, diabetes, hepatitis C, and primary biliary cirrhosis. Medications have now emerged as a major cause of mitochondrial damage, which may explain many adverse effects” — Neustadt and Pieczenik authors of Medication-induced Mitochondrial Damage and Disease
~~~~~~~~~~~~~~~~~~~~~~
“Establishing mitochondrial toxicity is not an FDA requirement for drug approval, so there is no real way of knowing which agents are truly toxic.” – Dr. Katherine Sims, Mass General Hospital – http://www.mitoaction.org
“It is difficult to get a man to understand something, when his salary depends upon his not understanding it!” – Upton Sinclair, anti-fascist, anti-imperialist American author who wrote in the early 20th century.
“No vaccine manufacturer shall be liable…for damages arising from a vaccine-related injury or death.” – President Ronald Reagan, as he signed The National Childhood Vaccine Injury Act (NCVIA) of 1986, absolving drug companies from all medico-legal liability when children die or are disabled from vaccine injuries.
Live Science is reporting that more parents are refusing to vaccinate their children now than a decade ago because they simply do not see a need for vaccination. Researchers have found that in 2013, 87 percent of pediatricians surveyed said they encountered vaccine refusals from parents of their patients, up from 75 percent of pediatricians who said the same in 2006.
Intelligent parents who refused to vaccinate their kids understand how unnecessary and dangerous vaccines are and such parents see the payoff, their kids tend to remain healthier with less colds and infections. Vaccine-preventable diseases are rare these days and many of them started to disappear before vaccines where created for each specific disease.
Live Science is biased when it comes to vaccines so it is not surprising that they say that many parents delay vaccination out of the mistaken belief that vaccines may burden children’s immune systems. There is no mistake about it. Vaccines do reduce natural immunity and can clobber the immune system causing death or many chronic diseases.
“The term “iatrogenic” means doctor, drug or surgery-caused disease. It is a taboo subject in America today.”
I don’t know how many of my readers listen to John Gilbert’s daily talk show on Duluth’s local KDAL radio station (610 AM). John is the journalist that writes the best sports-related columns that I have ever read. Those sports columns appears every week in the Duluth Reader, which is where my Duty to Warn column is published; so we are colleagues. John is a wonderful radio interviewer who occasionally invites me to appear on his “The John Gilbert Show” when medical issues arise. The show is on every weekday morning from 9 – 11 am. It is archived at www.kdal610.com/podcasts/the-john-gilbert-show-podcast/).
This morning (8-16-16), just before I was about to begin writing this week’s column, John called and asked me to appear on the show to give my medical opinion about the dramatic recovery of dementia victim Kris Kristofferson, the legendary singer/song-writer who had been erroneously diagnosed with incurable late-stage Alzheimer’s dementia (of unknown origin).
John had seen Kristofferson perform onstage with Merle Haggard a year or two ago when he was obviously seriously demented (although still able to remember the lyrics of his own songs). And then, just recently, John again saw Kristofferson perform in a solo concert when his dementia symptoms had completely disappeared! Reader publisher and editor Bob Boone graciously provided the $70 dollar tickets for John and his wife Joan.
Apparently Kristofferson had been mis-diagnosed with Alzheimer’s dementia about three years ago, which started more than one medical misadventure for he and his neurologists that involving neurotoxic medication trials with drugs. Those drugs that Kristofferson was treated with had been approved by the FDA on the basis of a couple of short-term trials involving only a few hundred so-called “Alzheimer’s Dementia” patients. The results that were submitted to the FDA showed only minimal improvement (albeit “statistically significant”), but only in mild to moderate dementia. Thus treating severely demented patients with those drugs was not FDA-approved (“off-label”). More
“The FDA (US Food and Drug Administration) tests all new psychiatric drugs”
False. Actually the FDA only reviews studies that were designed, administered, secretly performed and paid for by the multinational profit-driven drug companies. The studies are frequently farmed out by the pharmaceutical companies by well-paid research firms, in whose interest it is to find positive results for their corporate employers. Unsurprisingly, such research policies virtually guarantee fraudulent results.
Myth # 2:
“FDA approval means that a psychotropic drug is effective long-term”
False. Actually, FDA approval doesn’t even mean that psychiatric drugs have been proven to be safe – either short-term or long-term! The notion that FDA approval means that a psych drug has been proven to be effective is also a false one, for most such drugs are never tested – prior to marketing – for longer than a few months (and most psych patients take their drugs for years). The pharmaceutical industry pays many psychiatric “researchers” – often academic psychiatrists (with east access to compliant, chronic, already drugged-up patients) who have financial or professional conflicts of interest – some of them even sitting on FDA advisory committees who attempt to “fast track” psych drugs through the approval process. For each new drug application, the FDA only receives 1 or 2 of the “best” studies (out of many) that purport to show short-term effectiveness. The negative studies are shelved and not revealed to the FDA. In the case of the SSRI drugs, animal lab studies typically lasted only hours, days or weeks and the human clinical studies only lasted, on average, 4- 6 weeks, far too short to draw any valid conclusions about long-term effectiveness or safety!
Hence the FDA, prescribing physicians and patient-victims should not have been “surprised” by the resulting epidemic of SSRI drug-induced adverse reactions that are silently plaguing the nation. Indeed, many SSRI trials have shown that those drugs are barely more effective than placebo (albeit statistically significant!) with unaffordable economic costs and serious health risks, some of which are life-threatening and known to be capable of causing brain damage.
Myth # 3:
“FDA approval means that a psychotropic drug is safe long-term”
False.Actually, the SSRIs and the “anti-psychotic” drugs are usually tested in human trials for only a couple of months before being granted marketing approval by the FDA. And the drug companies are only required to report 1 or 2 studies (even if many other studies on the same drug showed negative, even disastrous, results). Drug companies obviously prefer that the black box and fine print warnings associated with their drugs are ignored by both consumers and prescribers. One only has to note how small the print is on the commercials.
That’s what mainstream press such as the LA Times and Reuters are reporting, based on a new study published in a respected medical journal, PLOS Medicine, which found young adults between the ages of 15-24, were nearly fifty percent more likely to be convicted of a homicide, assault, robbery arson, kidnapping, sexual offense and other violent crime when taking the antidepressant than when they weren’t taking the psychiatric drug.
To have heavy-hitters like the Los Angeles Times cover the issue is precedent setting, as the link between psychiatric drugs and violence has long been ignored by mainstream press. But the fact that antidepressants cause violence isn’t a new revelation as the Citizens Commission on Human Rights (CCHR) has been at the forefront of exposing this connection for nearly two decades.
Watch the video: “CCHR: By 1991 Antidepressants were known to cause
violence & suicide”
CCHR’s efforts to expose the link between violence and antidepressants goes back to 1991 when CCHR helped organize hearings before the Food and Drug Administration (FDA), where victims and experts gathered to testify that Selective Serotonin Reuptake Inhibitors (SSRIs) cause not only suicide but violence, including homicide.
The testimony by parents, about the violent self-inflicted deaths of their young children, was gut-wrenching. Yet, despite overwhelming data provided by experts, and the first-hand accounts of suicide and violence caused by antidepressants, the FDA Advisory Committee, many of which had financial conflicts of interest with the pharmaceutical companies, refused to warn the public of the link between suicide and antidepressants, and did not provide any consideration of whether the antidepressants may be responsible for other violent behavior.
But, as was expected, increasing numbers of suicides and other violent acts continued to add up and, finally, more than a decade later, in 2004, the FDA was, again, forced to address the issue. This time, though, the data provided by whistleblowers within the industry could not be shrugged off and more than a decade after the federal agency first knew of the deadly consequences associated with SSRIs, a “black box” warning for suicidal ideation and behavior finally was issued on all antidepressants. Yet the connection to violence and homicide continued to be ignored. To this day, despite 22 warnings on psychiatric drugs causing violence from international drug regulatory agencies, and despite the fact that t least 35 school shootings and/or school-related acts of violence have been committed by those taking or withdrawing from psychiatric drugs resulting in 169 wounded and 79 killed, the FDA has never issued black box warnings on antidepressant drugs causing violence. More
On August 18, 2015, the FDA proudly announced that they had approved (after 2 previous rejections) a new drug whose generic name is flibanserin (Addyi will be the brand name when it comes to your local drug store in mid-October). The only drug that Sprout Pharmaceuticals has ever marketed, flibanserin is purported to treat a “disease” called hypoactive sexual desire disorder (HSDD). The drug has been approved only for pre-menopausal women. The company will offer the drug in a 100 mg dose, to be swallowed once per night, no matter if sexual encounter is anticipated or not. This pill is not a female Viagra!
In a related story, two days after the FDA’s formal approval to market their only drug, Sprout announced that it had sold itself to a wholly-owned subsidiary of Valeant Pharmaceuticals International, Inc. for $1 billion dollars cash plus a portion of future earnings.
Below is some essential background information about the drug that hasn’t been well covered in the mass media. Every interested patient (and their prescribing practitioners) should know about this information before they ask for a prescription from their psychiatrist, OB-GYN, internist, family physician or nurse practitioner.
Some of the downsides of this new, soon-to-be blockbuster drug
For one thing, the drug will be expensive, indeed, it will unaffordable unless health insurance companies can be hood-winked to pay for it. If they do, look for premiums to rise! Cindy Whitehead, the CEO of Sprout has stated that it will be charging pharmacies $400 for a 30 pill supply [which equates to over $13 per pill!]. Nobody knows what the mark-up will be at the pharmacy.
There isn’t much that feels more self-reliant than going out to your backyard hen house to get fresh eggs for breakfast. There’s no need for USDA approval, you know what your hens have been eating, and you don’t have to pay a premium price and hope that the farm who raised the chickens that laid those grocery store eggs actually treated the hens humanely. Bonus points if the bacon you fry up comes from a local farm, and bonus BONUS points if you raised that little piggie yourself. Raising backyard chickens is incredibly rewarding.
It’s pure freedom, this control over your own food.
Of course, until you have to register your chickens. Then, as food freedom activist Joel Salatin says, “Everything I want to do is illegal.”
With so many people moving towards self-reliance, you had to know it was only a…
“Lenzer refers to a report by the Institute for Safe Medication Practices: “It calculated that in 2011 prescription drugs were associated with two to four million people in the US experiencing ‘serious, disabling, or fatal injuries, including 128,000 deaths.’”
The report called this “one of the most significant perils to humans resulting from human activity.”
There are several reasons why the medical cartel is too big to fail: the enormous amount of money at stake; its aim to control populations.
In this article, I want to examine a related reason.
Suppose it was discovered that thousands of bridges around the US were in imminent danger of collapsing? Not because maintenance and repair were lacking, not because the materials used to build them were cheap and shoddy. But because the original designs were inadequate and broke basic rules of engineering.
Suppose five or six major manufacturers built their automobiles so the vast majority of power derived from the engines was transferred to one wheel?
The infringement of medical rights and normal access to necessary types of pain medicine has been an ongoing issue for many years. How is it that the FDA (Food and Drug Administration) or the DEA (Drug Enforcement Administration), an unelected agency, has the legal authority to deny effective prescription pain killers by a doctor for a patient? Are these agencies more knowledgeable than the MD’s or is it politics as usual?
Countless patients who plead their case with their doctors are now suffering needlessly from excruciating pain because these agencies which are an arm of the federal government are presently restricting the use of certain prescription drugs that may be addictive. Drugs such as Vicodin(Hydrocodone), a pain reliever, was taken off of the market because it was found not only to be addictive but it also caused liver cancer. Yet, there are many other drugs, depending upon the frequency of their usage, that present other problems. Also, while medical marijuana is seen as a pain reliever, it has also been shown in studies to be addictive and also causes cancer. So what else is new. People who are denied pain relievers for certain ailments are also given regular doses of morphine which will, in the end be fatal.
Here is the case of the late, Ms. Siobhan Reynolds, founder of the Pain Relief Network. The Network was an advocate for adequate pain medication for patients and against the regulations and the negligent
behavior of those agencies such as the FDA and DEA. Doctors who are willing to provide for their patients are now under more scrutiny from these federal agencies when it comes to prescribing pain medicine. Ms. Reynolds whose recommendations would undercut the ability of federal agencies that violate the medical rights of American citizens were not heard.
Countering her recommendations at the time, the Assistant U.S. Attorney Tanya Treadway attempted to silence Reynolds with a gag order in the case of Dr. Stephen Schneider, who was indicted for “illegal drug trafficking” in December 2007. The gag order was very properly denied, but the U.S. Attorney’s Office responded with an inquisitorial and malicious Grand Jury proceeding against Reynolds, which bankrupted her organization. Although Grand Jury proceedings are secret in order to protect defendants, Reynolds’ desire to make all records public has been improperly denied, apparently in order to protect, not her innocence, but the guilt of the prosecutors.
Later, the Obama administration moved to restrict prescriptions of the most commonly used narcotic painkillers in the U.S. in an attempt to curb widespread abuse. Also, the DEA said it would reclassify
hydrocodone combination drugs such as Vicodin and put them in the category reserved for medical substances with the highest potential for harm.
In summary, if you or persons that you know are suffering from needless pain because your doctors are reluctant to administer certain pain medications, you now know the reason.
Submitted By Dr. Gary Kohls
By Guest Columnist William Annett
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“(c) The greatest boff of all belongs to the pharmaceutical industry and its standard-bearer GlaxoSmithKline (GSK). Normal operations, sanctioned by a well-juiced government and its trained seal the FDA, consist of developing top-drawer medications which are then marketed for billions, whether or not they’re dangerous – or even criminal.”
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We’re living in a cuckoo’s nest that would have baffled Ken Kesey. Consider just three items at the top of our agenda.
(1) Astronomical military spending at a time when there’s nobody left in the world big enough to fight us, with the exception of international terrorists (of which the definition is any rebel faction in a Middle East loaded with factions, most of which we first created, then armed and now oppose, not because they’ve changed but because we have),
(2) the health care farce, which makes us the most expensive, least effective (at least #47 in the world) and largest laughingstock in the world, and finally,
(3) the final triumph of corporate governance in Washington, which is icing the decline and fall of both capitalism and democracy in one fell swoop.
Witness the final humiliation: Warren Buffett, the richest deckhand on this ship of fools, recently announced how he could cure all our ills in about five minutes: every time Congress screws up by deadlocking itself or filibustering over the people’s business, we suspend their Congressional salaries and munificent benefits, such as the real health care system they deny us. The result would be guaranteeing the immediate end of deficits, debt problems and unemployment. Inadequate, Warren, but like drowning lawyers, a good start.
Take the Pentagon (as Rodney Dangerfield might say: Please). While every politician is shit-hemorrhaging over the budget deficit, military spending has reached such ridiculous proportions that multi-billion dollar items (such as the recent F-35 horror) click automatically into place, even though nobody – including the Pentagon brass itself – wants the bloody thing. It’s just fixed, embedded national policy/corporate welfare that subsidizes the weapons industry. And just the other day, our formerly audacious hopeful President sent to Congress his endorsement of the largest Pentagon budget in history. More
The current dearth of treatment options for Ebola is not from a lack of options, but from a zealous protection of current medical monopolies together with an overabundance of red tape.
In a related article, we discussed government hostility to natural remedies that are both cheap, effective, and more readily available. In this article, we’ll look at the FDA roadblocks to more conventional treatments.
The FDA is paid by drug companies and is generally friendly to them. Even so, getting a new drug or device approved is a torturous and insanely expensive process. The minimum cost these days is several hundred million dollars spent over many years. The average cost is in the billions.
Technology like Nanobiosym’s “iPhone-sized device,” which can be used to detect Ebola and other diseases in less than an hour, is being delayed by needless FDA red tape. The Dallas hospital that treated three patients with Ebola had a similar device, one that could detect Ebola with high degree of confidence within a few minutes, but were prevented from using it because of FDA regulations. More
If you worked for a federal agency that was killing people at the rate of 100,000 a year, every year, like clockwork, and if you knew it, wouldn’t you feel compelled to say or do something about it?
At the FDA, which is, in fact, killing Americans at that rate, no one has ever felt the need to step forward and speak up.
Let’s shift the venue and ask the same question. If you were a medical reporter for a major media outlet in the US, and you knew the above fact, wouldn’t you make it a priority to say something, write something, do something?
I’m talking about people like Sanjay Gupta (CNN, CBS), Gina Kolata (NY Times), Tim Johnson (ABC News), and Thomas Maugh II (LA Times).
And with that, let’s go to the smoking guns. The citation is: BMJ June 7, 2012 (BMJ 2012:344:e3989). Author, Jeanne Lenzer.
Lenzer refers to a report by the Institute for Safe Medication Practices: “It calculated that in 2011 prescription drugs were associated with two to four million people in the US experiencing ‘serious, disabling, or fatal injuries, including 128,000 deaths.'” More
“We cannot continue to rely on our military in order to achieve the national security objectives that we’ve set. We’ve got to have a civilian national security force that’s just as powerful, just as strong, just as well-funded.” –Barack Obama, “Obama’s Civilian National Security Force“
The civilian national security force was never intended to be populated by private citizens, but rather, by hired citizens who could be convinced to violate the constitution, and your rights simply by virtue of wearing a tin badge and told they were not constrained by anything as marginal as the law.
By now it should have become obvious, that rather than just using our military to attack us in-country, it is far more effective to militarize various federal and state agencies and have them do the attacking under cover of the agency. Claiming they are defending the law, upholding statutes and regulations, military style swat teams from numerous federal agencies have been steadily attacking, threatening and harassing private citizens. These attacks are nothing less than acts of war perpetrated by the federal agencies on behalf of the federal government.
That terrorist you are so afraid of is your neighbor
“If you see something…Say Something”…I would like to report that the terrorists we need to fear are inside the gates.
They were our neighbors, our family members; now unrecognizable as the transformation from ordinary citizen to badge heavy, agency employed, domestic terrorist takes place. And these people are domestic terrorists by any definition. They do not work for “we the people”, but rather, for corporate interests both foreign and domestic. They will willingly violate the laws you are required to comply with, without blinking an eye. The constitution? Your rights? Not even a consideration.
The Civilian National Security force that Obama was speaking about was created under the fake food safety bill passed in 2010, via “Dirty Harry” Reid’s infamous, unanimous and singular vote. Without objection! Every one of the remaining 99 Senators voluntarily vacated the senate chamber to facilitate “Dirty Harry’s” one unanimous vote. Every other Democrat and Republican senator was in on the deal.
“Then, on the floor of the Senate in the late afternoon, early evening of Sunday, December 19, Senator Reid called the Recycling bill for a vote and there was no objection from the two other Senators who were on the floor. So by unanimous consent HR 2751 was passed. Then Senator Reid moved for reconsideration with the vote to be tabled. This was granted by the same unanimous consent because there was no other Senator on the floor. Then Senator Reid offered without objection amendment number 4890 which substituted S. 510 the Food Safety Bill for the Recycling Bill. Without objection, then the amendment was passed and the Food Safety Bill had been substituted for the Recycling Bill. Reid moved that the bill be read for the third time and asked for the question. Without objection, the bill passed, and the Food Safety Bill was on the way back to the House.”
The result? The militarization of federal agencies in preparation for the coming assaults on family and independent food producers and on private property rights. This bill had little to do with food safety and much to do with assembling the in-country attack units now employed by USDA, FDA, EPA and the notoriously corrupt BLM. More
Note: Where was Senator Durbin when Vioxx killed an estimated 500,000 people? Where is he when the FDA approves as safe and effective, medications and vaccines that kill or permanently harm individuals? He is nowhere to be found! Supplement manufacturers are already restrained from making unfounded claims. And, supplements are not protected by the FDA so-called “rates of acceptable deaths” associated with big pharma . Personally, I think we should demand that government officials be labeled… toxic and dangerous!
Durbin’s bill, S 1310 The proposed law trusts the FDA and the Institute of Medicine (IOM) to decide what levels and combinations of dietary ingredients are considered safe and what aren’t. Given the FDA’s profound bias against supplements, and the skewed, anti-science recommendations of the IOM’s recent vitamin D report, these are hardly trustworthy sources of guidance!
Today, just as Congress is preparing to recess until the second week in September, Sen. Dick Durbin (D-IL) reintroduced legislation that would deal a deadly blow to nutritional supplements.
This bill is a naked new FDA power grab—an attempt to move us one step closer to a full FDA pre-approval system for supplements. That, of course, would just make supplements insanely expensive, like drugs—if you could get them at all.
URGENT! Please write to your senators immediately and tell them to stop Sen. Durbin’s frontal attack on your right to use supplements dead in its tracks! We don’t need this new legislation—all we need is for existing laws to be fully enforced. We do need our access to nutritional supplements to be protected.
Tell Your Senators to Oppose Sen. Durbin’s Dietary Supplement Labeling Act
The Dietary Supplement Labeling Act has been introduced in the in the Senate by Sen. Dick Durbin (D-IL). The bill targets nutritional supplements and supplement manufacturers in an effort to pass unnecessary new regulations and give the FDA vast new powers.
This bill requires that the FDA, together with the Institute of Medicine, compile a list of dietary ingredients (supplements) that could lead to adverse events or are otherwise deemed risky in some way. But creating lists of “bad” ingredients or “bad” doses based on completely arbitrary or non-existent standards is a slippery slope. Please do not be misled. This is not a minor change to DSHEA. It will give the FDA major new powers to curtail supplement sales. It will lead inexorably to pre-approval for supplements—and that will cost so much that most supplements will disappear.
Moreover, almost all of the bill’s other provisions are already covered by existing law. There is no need for any new legislation, especially with the vague language in this bill; the only need is for existing laws to be fully enforced. Sign petition HERE!
“Why is it, every time the jackasses in the District of Criminals have run some program into the ground, squandered massive amounts of dollars while letting corporations write bills that benefit them and rape and rob the states, they always come out and say; “The system is broken”. “We’ve got to fix the system, it is broken”. It’s an emergency! We have to do something right now! And that is all quickly followed by one phony “crisis” after another as they try to scare the public into believing the “crisis” just magically and mysteriously appeared.”
Recent news reports highlighted the announcement of a proposed restructuring of the United States government (USA.Inc.). The collusion of privately owned federal corporations that operate under fraud, color of “law”, and fictions of law, are now openly conspiring with other Non-governmental agencies in an effort to by-pass any remaining restrictions on their plundering and theft of the states assets and adherence to UN Agenda 21, Chapter 8. The conversion to a one-world government where the individual not only will not be able to own anything, but can be found at any time to have violated some or all of the 23 million fictionally created rules, regulations, statutes or codes, issued by government and private corporations against the people, will be expanded.
An overt act of treason against the people of the sovereign states, is underway. Un-elected bureaucracies, created for no other reason than to by-pass Constitutional provisions and prohibitions against a centralized all-controlling government have been published in a study called Sustainability For the Nation: Resource connections and government linkages. This is a blueprint for finalizing the destruction of our Constitutional Republic, centralizing all power in one branch and totally dis-empowering the people then rendering the Constitution dead once and for all, and structuring the foundations for one world government.
Should the provisions in this study be implemented to any degree, pink slips should be sent to every member of Congress, in both houses, terminating their cushy and highly protected jobs for allowing this to transpire. This study represents a bold-faced attack on the Constitution, the rule of law and the people of the states. What this study details is the establishment of a Homeland Security Terrorism type behemoth federal monstrosity which will quickly show itself to be a threat to the nation, just as Homeland Security Terrorism has done.
I find it less than coincidental that Senator Durbin, in his dramatic speech on the floor of the Senate, proposed to Senator Coborn, who objected to S.510, that maybe what was needed was just one big agency to cover everything. Wonder where he came up with that idea? Just a notion; top of his head suggestion.
When those who subscribe to the phony “sustainability” plan describe what they think it entails, always it is some sense of environmental protection, some social equalization or some possible greening up of the planet for the sake of humanity. The word “sustainability” is another of what we like to call “weasel word swaps”. (think corporate government trade agreements (contracts) as opposed to Constitutionally approved treaties. Two entirely different concepts one binding and the other simply complied with. More
The state of Minnesota just recently passed a ban on formaldehyde in certain “children’s products.” Wait a minute; aren’t childhood vaccines children’s products?
Minnesota Governor Dayton signed Bill HF 4581 on May 13, 2013, that bans formaldehyde in certain children’s products. The law defines children’s products as a product primarily designed or intended by the manufacturer to be physically applied to or introduced into a child’s (defined as a person under eight years of age) body, including any article used as a component of such a product. Excluded from the definition of a children’s product is food, beverage, dietary supplement, pharmaceutical product or biologic, children’s toys that are covered by the ASTM F963, or a medical device as defined in the federal Food, Drug, and Cosmetic Act.
Following are the key requirements of the rule: More
We have long maintained that the FDA is a threat to public health. Routinely approving drugs for use on the public that they have neither tested nor questioned, tens of thousands of people die each year as a result. No one is prosecuted. No one is held accountable. Not one pharmaceutical CEO will be held accountable or liable.
At best, this is racketeering. At worst, it is aiding and abetting in mass murder.
This agency, which has been responsible for more deaths than many wars, the hyped up gun arguments, and assorted other hot button topics, has never once been smacked down for its collusion with its pharmaceutical corporate partners. And never once has it been held liable for the massive number of deaths that are a result of its “for profit at the expense of human life” business practices.
About half of the drugs put into the market will be recalled in five years because they cause death, heart attacks and numerous other adverse effects…..and not one FDA “I was just following orders” employee on any level will see one day in jail.
Maybe public hangings should be reconsidered. How many people are going to be seriously harmed or die before we close this abomination down?
Did you know that if a supplement company “Likes” a customer’s Facebook post, it magically transforms nutritional supplements into drugs? The same thing happens if a supplement’s website links to a scientific article!
As recently as this week, the FDA has made attacks like these to expand the agency’s definition of “disease claim.” Why? By saying a supplement makes a disease claim, the FDA can call it a “drug”—and then remove it from the market!
This also has scary implications for the government regulation of Internet searches and speech. If supplement companies start deleting customer comments out of fear of FDA action, then the FDA has effectively limited consumer speech by using the company as a censorship puppet.
It doesn’t stop there: the FDA has something called its Evidence-Based Review System. It’s just a backdoor tactic to require prohibitively expensive studies—as in hundreds of millions of dollars—if companies want to make any claim about the science behind their supplements. Because natural products can’t be patented, supplement companies can never recoup these astronomical costs. Only Big Pharma and their blockbuster drugs can afford to “pay-to-play:”
We’ve had enough. How about you?
Here’s our plan: ANH-USA will submit multiple petitions—strategically supported by our ongoing legal activities—to address, from various angles, FDA’s egregious First Amendment violations. If we win, we ALL win. If the petitions are denied, we’re ready to pursue further litigation.
Immediate action is critical. Unfortunately, this is an expensive project. This is why we need your help!
Our goal is to raise $40,000 by June 14, so we can
kick off our FDA petitions to defend free speech
and supplement access.
The FDA’s actions leave consumers in the dark about the dietary supplements they are buying for themselves and their families. This can be a matter of safety—for you and the ones you love.
The FDA is halfway down the slippery slope of taking away consumer access to supplements. Will you join us in saying, “Enough is enough!”? More
The letter below was received from Rep. Collin Peterson, 7th District, Minnesota. Peterson’s letter details his love of gmo’s and his belief that no science exist to substantiate the claims that gmo is harmful to human health. With numerous countries around the world banning the use of gmo seeds, the importing of gmo products into their countries, and the massive number of scientific studies that were actually done to document the threat to the environment and public health that these frankenfood creations are causing, it appears Mr. Peterson is oblivious to all. Makes you wonder what planet this guy is on.
Thank you for contacting my office about genetically engineered foods. I appreciate hearing from you.
Dear Mr. Peterson: I doubt that you appreciate hearing from me or anyone else who isn’t on the bio-piracy wagon. I am fully aware that this is a very lucrative association for you , not only politically, but personally as well.
Since the first genetically engineered crops became commercially available in the mid-1990s, U.S. soybean, cotton, and corn farmers have rapidly adopted them.
Farmers have not rapidly adopted genetically engineered crops unless you considered being coerced, bullied, terrorized, threatened with lawsuits or finding that bio-pirates such as Monsanto have monopolized the market and have the Supreme Court of The United States firmly in their pocket and also a cushy little seat in the White House to protect their interests, willing adoption of these crops.
Since that time there has been no scientific evidence suggesting that these crops are harmful. More
By: Dr. Gary Kohls
FINALLY — Comprehensive, authoritative information about vaccine exemptions you can trust, from Alan Phillips, J.D., a leading vaccine rights attorney with years of experience helping clients throughout the U.S. legally avoid vaccines in a wide variety of vaccine-refusal settings. Recommended By Dr. Tenpenny
The PPJ Gazette 