Showing posts with label FDA. Show all posts
Showing posts with label FDA. Show all posts

Tuesday, April 10, 2018

Curtailing Cures?

Curtailing Cures? | essential-oil | FDA Medical & Health Natural Medicine Petitions Special Interests


For more than 25 years, the U.S. Food & Drug Administration (FDA) has relied on established clear and enforceable standards for the manufacture and sale of homeopathic medicines in the U.S.


Now the FDA wants to withdraw this standard and replace it with a vague enforcement policy. Without clear guidance on what is legal, regulatory enforcement quickly becomes arbitrary and capricious.


Why is the FDA taking this step? We’re not sure. All the FDA says is that there has been a significant increase in products labeled as homeopathic.


Homeopathic medicines are used by millions of Americans and their kids. These remedies gently stimulate the body to heal itself, and are safe, natural and without side effects.


In an era where the U.S. healthcare system ranks dead last among industrialized nations, based on things like quality of care, access to doctors and equity throughout the country, consumer choice is more important than ever.


Could the FDA be trying to limit access to homeopathic medicines in favor of protecting the $446-billion pharmaceutical industry?


TAKE ACTION: Don’t Let FDA Needlessly Restrict Your Access to Homeopathic Remedies!


h/t: The Organic Consumers Association


The post Curtailing Cures? appeared first on The Sleuth Journal.

True Healing: Beyond “Managing”, “Treating” And “Curing” A Disease

True Healing: Beyond “Managing”, “Treating” And “Curing” A Disease | harmony-spa-natural-medicine | Big Pharma Medical & Health Natural Medicine Sleuth Journal Special Interests

True healing occurs at deep levels. It integrates and makes whole. It is beyond just “managing”, “treating” or “curing” disease, and unless they change their perspective, it will continue to be beyond Big Pharma and Western medicine too.


True healing and true health are deep concepts which by their very definition imply oneness and unity (the word heal is etymologically derived from various words such as the Old English hælan meaning “to make whole”). True healing includes the many levels within you beyond just the physical – the integration of the emotional, sexual, mental, spiritual and other selves or layers. True healing is far beyond just “managing”, “treating” and “curing” disease, which Big Pharma and its lapdog the FDA like to focus so exclusively upon. Western medicine has its place in society as an excellent tool for specialized surgical or other emergency interventions – however it came into being from the Rockefeller-Big Pharma cartel, whose business model thrives on repeat customers who can’t get off the hamster wheel of drug after drug after drug. On a deeper level, is it really any wonder that Western medicine can’t deliver true healing, when its approach is narrow and materialistic, rather than broad and holistic – when it’s fixated on managing, treating and curing, rather than healing?


Big Pharma and Western Medicine: Hooked on “Treating” Disease


True Healing: Beyond “Managing”, “Treating” And “Curing” A Disease | true-healing-big-pharma-hooked-on-treating | Big Pharma Medical & Health Natural Medicine Sleuth Journal Special Interests

Hooked on “treating” disease, but not going any further.


If you’re wondering where the notion of “treating” come from, look no further than the FDA-mandated disclaimer that many natural health and holistic practitioners and companies are forced to use on their products. It states that “this product is not intended to diagnose, treat, cure or prevent any disease” because only a drug can legally make such a claim. And, in a great example of FDA circular logic, if a substance does have an effect on the human body such as preventing or curing a disease – then it must be drug and not a food!


Guess what? The moment something becomes a drug and not a food, it’s regulated differently. If you’re a producer of a food that wants to state its natural effects on the body, now you have to jump through all sorts of expensive hoops just to state the truth. This is despite the fact that scientific studies have shown, for instance, that cherries have a positive effect on gout and arthritis, coconut oil on Alzheimer’s, and turmeric, spirulinagraviola/soursop on cancer. It is an upside-down, outrageous situation where people are being silent about the clear and scientifically provable effects of foods and other natural medicines out of fear of being sued into poverty, taken down or taken out. Ignorant people defend the Big Pharma system by claiming it’s backed by “science”; meanwhile, insiders and experts state categorically that most scientific research is fraudulent, and most science is actually corporate junk science that is paid to produce the results its funders want.


Managing Disease: A Big Pharma Specialty


True Healing: Beyond “Managing”, “Treating” And “Curing” A Disease | true-healing-big-pharma-management | Big Pharma Medical & Health Natural Medicine Sleuth Journal Special Interests

True healing has nothing to do with disease management, Big Pharma style.


The truth is that managing disease is a Big Pharma specialty. The most profitable customers are those patients who are going to be reliant on prescription drugs – just to exist – for the rest of their lives. In those cases it’s all about managing disease. How interesting that the word itself management is a very corporate word. Another aspect of the managing of disease is all the unnecessary (but very fancy and impressive sounding) testing that is done to people, under the guise of “early detection”. In his revealing book Confessions of a Medical Heretic, Dr. Robert Mendolsohn quotes an article entitled “Cleveland’s Marvelous Medical Factory” which boasted of the Cleveland Clinic’s “accomplishments last year: 2,980 open-heart operations, 1.3 million laboratory tests, 73,320 electrocardiograms, 7,770 full-body x-ray scans, 24,368 surgical procedures.”


Seems wonderful … except for the very obvious point that none of these procedures has been proven to have anything to do with restoring health or true healing. When people get screened for a disease, they are being subjected to dangerous radiation (more money for the Rockefellers) which harms tissue and can end up causing the exact disease it is supposed to be protecting against – as happens daily with the mammogram scam, designed to drum up new breast cancer clients.


Healing vs. Curing


True Healing: Beyond “Managing”, “Treating” And “Curing” A Disease | true-healing-vs-curing | Big Pharma Medical & Health Natural Medicine Sleuth Journal Special Interests

Healing vs curing: there is a difference. Healing takes into account the energetic and holographic nature of our body and reality.


At this stage you may be thinking: well, Big Pharma and Western medicine do a lot of “managing” and “treating”, but aren’t they also in the business of “curing”? Yes – but even in this case, Western medicine is falling short of the ultimate goal of healing. Curing a disease and healing a disease are different things. As this website Healing Through The Arts states:



Curing is what medical science attempts to do through medication, treatment and external intervention. It usually is the result of a series of treatments that hopefully lead to an event – the absence of disease.


Healing is an internal process you do for yourself. Healing restores the balance and harmony to the body, mind and spirit. It can be done without a cure. Healing activities are essential when the negative influences of illness, loss or life changes encompass your life.”



The website MindBodyGreen states:



Curing is a restoration of health, an absence of symptoms, and a remedy of disease. Healing, on the other hand, is a restoration of wholeness — not the level of wholeness before the diagnosis, but a restoration of wholeness that is new, different, and comparatively better than before the onset of disease. Healing is not the removal or cessation of symptoms, but rather an integrative process that transcends the physical and includes mental, emotional, and spiritual vitality and wellness.”



Others have defined curing as the “elimination of all evidence of disease” and healing as “becoming whole”. There are many ways to conceive and verbalize the difference between curing and healing, but the overall point is that healing is a deeper concept which includes the understanding that we are not just physical beings. If we want to attain true health, we must address all the levels of our being. Often a “disease” is merely an outer physical manifestation of a psychological, energetic or spiritual blockage which is taking place at a much deeper level.


Big Pharma has (rightly) been accused of making drugs that just mask symptoms without healing the underling cause. In many cases, they transfer the disease or imbalance from one part of the body to another. From a holistic perspective, this is only minorly helpful or not helpful at all, because as long as you have some imbalance, you’ve still got a health problem you have to deal with. So, even if Big Pharma actually cures your disease, rather than just treating it or managing it, you still aren’t really at a place of true healing, or real health and balance. If the cause of your disease is happening on an energetic level, how can drugs, surgery or radiation ever address it?


Towards True Healing


In conclusion, if you want true healing, look at all aspects of your entire life. Are you indulging in negative thought patterns? Are you involved in toxic relationships? Are you getting the right type, frequency and duration of exercise? Are you sleeping well? Is your lifestyle too sedentary? Are you allowing questionable food items into your diet? How are you dealing with stress? Even if you are doing a good job on most of these, being weak in one of these areas may be enough to throw your system off balance and lead to disease. We’re all on a journey of remembering our true selves, and reclaiming our wholeness through true healing is an inseparable part of it.


Sources:


Western Medicine is Rockefeller Medicine – All The Way



http://www.fda.gov/Food/DietarySupplements/QADietarySupplements/ucm191930.htm#FDA_oversight


http://www.ncbi.nlm.nih.gov/pubmed/?term=cherry+arthritis


http://www.ncbi.nlm.nih.gov/pubmed/?term=coconut+oil+alzheimers


http://www.ncbi.nlm.nih.gov/pubmed/?term=turmeric+cancer


http://www.ncbi.nlm.nih.gov/pubmed/?term=spirulina+cancer


http://www.ncbi.nlm.nih.gov/pubmed/?term=soursop+graviola+cancer


Most Scientific Research of Western Medicine Untrustable & Fraudulent, Say Insiders and Experts



The Top 10 Tricks Used by Corporate Junk Science



http://www.whale.to/vaccines/mendelsohn2.html


http://www.naturalnews.com/027641_mammograms_breast_cancer.html


http://www.htta.org/curing-vs-healing


http://www.mindbodygreen.com/0-7961/whats-the-difference-between-healing-and-curing.html


The post True Healing: Beyond “Managing”, “Treating” And “Curing” A Disease appeared first on The Sleuth Journal.

Wednesday, February 21, 2018

Salmonella OUTBREAK: CDC Blames Herbal Supplement Kratom


An outbreak of salmonella in 20 states is being blamed on kratom.  According to the CDC, Americans should stay away from kratom for now, until the origin of the outbreak can be pinpointed.


According to federal government health agents, a popular herb called kratom is linked to an outbreak of salmonella that has made 28 people sick in 20 states. Eleven people have been sick enough to need hospitalization. The government agency, the CDC also claims the “most of the people who have been made seriously ill in the outbreak remember having recently used some form of kratom.” Most?


“At this time, CDC recommends that people not consume kratom in any form. The investigation indicates that kratom products could be contaminated with Salmonella and could make people sick,” the CDC says on its website.


Kratom has been the focus of a storm of controversy. The Food and Drug Administration has issued increasingly urgent warnings about the herb, saying it acts like an opioid drug and advising people to stay away from it. –NBC News


Kratom enthusiasts say it’s enjoyable to use recreationally, but they also say it is also useful for treating withdrawal symptoms from opioid use and can be used to treat pain. “Kratom is not a drug,” the American Kratom Association says on its website. “Kratom is not a drug. Kratom is not an opiate. Kratom is not a synthetic substance. Naturally, occurring Kratom is a safe herbal supplement that’s more akin to tea and coffee than any other substances.”


Kratom is a natural botanical native to tropical Southeast Asia that is part of the coffee family. It’s also known by its scientific name, Mitragyna speciosa. The people of Southeast Asia have used Kratom leaves as an herbal supplement and traditional remedy for hundreds of years. When taken in appropriate amounts, Kratom can provide increased energy, minor pain relief and many find relief from a variety of other mental and physical ailments. Today, people in the U.S. are consuming Kratom, as they do other herbal supplements and traditional remedies. –American Kratom Association


Salmonella is a very common bacteria that causes what we all know as food poisoning. The CDC says it is not clear how the bacteria could have gotten into supplies of kratom. But genetic testing links the cases that have been reported. Salmonella has been linked to supplements before and caused an outbreak in food powder in 2016.


“In interviews, ill people answered questions about the foods they ate and other exposures in the months before they became ill. Eight (73 percent) of 11 people interviewed reported consuming kratom in pills, powder, or tea,” the CDC said.  There doesn’t appear to one particular brand or type of kratom taking the blame, just kratom in general.


The Salmonella bacteria could have been on the plant itself, before harvesting, or in the irrigation water used on the plants, said Benjamin Chapman, an associate professor and food safety specialist at North Carolina State University. It’s also possible that the supplements became contaminated with Salmonella somewhere during the manufacturing process, he said. (Salmonella bacteria typically live in animal and human intestines, and get into the environment through fecal matter, according to the Mayo Clinic.)

Tuesday, February 20, 2018

US Court Rejects FDA Appeal on GMO Salmon Approval Documents





US Court Rejects FDA Appeal on GMO Salmon Approval Documents | ge-salmnon | FDA General Health GMOs Special Interests


Last week, the U.S. Ninth Circuit Court of Appeals denied the FDA’s latest attempt to hide thousands of pages of key government documents related to the agency’s first-ever approval of genetically engineered (GE) salmon for human consumption. The court’s decision is a big win for public transparency and a firm rejection of the Trump administration’s position that it can unilaterally decide whether to withhold government documents from public and court review.


In 2015, the FDA approved a GMO salmon made from the DNA of three different animals: Atlantic salmon, deep water ocean eelpout, and Pacific Chinook salmon. The GE version is intended to grow faster than conventional farmed salmon, reportedly getting to commercial size in half the time.


Even though this is the first time any government in the world has approved a GE animal for commercial sale and consumption, so far the FDA has taken a lackadaisical approach to evaluating the salmon’s potential for harm to wild salmon and the environment. If the GE salmon were to escape, it could threaten wild salmon populations by outcompeting them for scarce resources and habitat, by mating with endangered salmon species, and by introducing new diseases.


If the GE salmon were to escape, it could threaten wild salmon populations by outcompeting them for scarce resources and habitat, by mating with endangered salmon species, and by introducing new diseases


The world’s preeminent experts on GE fish and risk assessment, as well as biologists at U.S. wildlife agencies charged with protecting fish and wildlife, heavily criticized the FDA for failing to evaluate these impacts. But the FDA ignored their concerns, so in March 2016, Earthjustice filed a lawsuit against the agency.


As part of the lawsuit, the FDA is required to compile a record of documents that illuminate the path the agency followed to reach its decision to approve the GE salmon—much like a student is required to show their work for a math problem in middle school.  A complete record is essential in all cases. But it is especially important here because the FDA has so far refused to release most of the documents related to its decision, despite repeated requests for that information from Earthjustice’s diverse set of clients under the Freedom of Information Act.







The post US Court Rejects FDA Appeal on GMO Salmon Approval Documents appeared first on The Sleuth Journal.

Wednesday, February 7, 2018

Tuesday, February 6, 2018

All Homeopathic Products Now Illegal?

All Homeopathic Products Now Illegal? | pill-506906_960_720 | FDA Government Government Control Losing Rights Medical & Health Natural Medicine Sleuth Journal






Story at-a-glance




  • In a draft guidance document released by the U.S. Food and Drug Administration (FDA), the agency takes aim at homeopathic remedies

  • In a reversal of a long-standing decision to treat homeopathic remedies differently from other drugs, the FDA has now labeled virtually all of these products as “new drugs” that are “subject to FDA enforcement action at any time”

  • Homeopathic products are now a close to $3 billion industry and such remedies have been shown effective for a variety of ailments, from the flu and allergies to vitiligo







About 5 million U.S. adults and 1 million U.S. children use homeopathy every year, and the remedies are known to be “generally safe and unlikely to cause severe adverse reactions,” according to the U.S. National Institutes of Health’s National Center for Complementary and Integrative Health.1 Yet, if the U.S. Food and Drug Administration (FDA) continues on its latest crusade, this natural health modality may soon be much harder to come by.


In a draft guidance document released in December 2017, the FDA takes aim at homeopathic remedies, or as they put it, “drug products labeled as homeopathic.”2,3 In a reversal of a long-standing decision to treat homeopathic remedies differently from other drugs, the FDA has now labeled virtually all of these products as “new drugs” that are “subject to FDA enforcement action at any time.”


FDA Declares Homeopathic Drugs Illegal, Plans to Ramp Up Enforcement Actions


While deaths from drugs like opioids are now a public health crisis, homeopathy has maintained a much lower, and presumably safer, profile. Yet, the FDA is using its limited resources to target the latter, citing a need to “protect consumers who choose to use homeopathic products.” Why now? The FDA also cited a “large uptick in products labeled as homeopathic that are being marketed for a wide array of diseases and conditions,” to the extent that homeopathic products are now a close to $3 billion industry.4


Perhaps that’s $3 billion too much for Big Pharma, FDA’s cozy partner in crime. “[I]n one fell swoop, the FDA has declared that virtually every single homeopathic drug on the market is being sold illegally,” the Alliance for Natural Health USA (ANH USA) wrote5 — and it’s not an exaggeration. In essence, the FDA’s guidance reads:6



  1. Any homeopathic drug that has not been considered “generally recognized as safe and effective” (GRAS/E) is considered a new drug

  2. FDA has not determined that any homeopathic drugs are GRAS/E

  3. A new drug cannot be marketed unless it goes through the FDA’s approval process

  4. No homeopathic drugs have gone through FDA approval nor can any producer afford to take them through the approval process


The FDA then states that it’s proposing a “new, risk-based enforcement approach” and first plans to target the “unapproved drug products labeled as homeopathic that have the greatest potential to cause risk to patients.” This includes:7

















Products with reported safety concernsProducts that contain or claim to contain ingredients associated with potentially significant safety concerns
Products for routes of administration other than oral and topicalProducts intended to be used for the prevention or treatment of serious and/or life-threatening diseases and conditions
Products for vulnerable populationsProducts that do not meet standards of quality, strength or purity as required under the law

FDA Does About-Face, ‘Penalizes an Entire Industry’


The draft guidance is a complete turnaround from the FDA’s prior stance on homeopathic remedies, which stated, under the 1988 Compliance Policy Guide (CPG) 400.400, Conditions Under Which Homeopathic Drugs May be Marketed, they did not need to get FDA approval prior to coming on the market. Instead, the ingredients in homeopathic remedies were to be verified by the Homeopathic Pharmacopoeia of the United States (HPUS). As noted by law firm Venable:8


Essentially, the HPUS creates a monograph for homeopathic drugs to follow, not dissimilar to the OTC drug monographs that FDA has developed for allopathic drugs. Accordingly, by virtue of an ingredient’s inclusion in the HPUS, the ingredient has already been closely examined and determined to be safe and effective by the HPCUS [Homeopathic Pharmacopoeia Convention of the United States].


Compliance with the HPUS functions as a premarket review of safety and effectiveness in the homeopathic context. By classifying homeopathic drugs as unapproved new drugs, the FDA is requiring a second showing of safety and effectiveness, a step that is unnecessary, not to mention impractical, given that the Agency intends to hold homeopathic products to an allopathic standard that is inappropriate, given the nature of homeopathic products.”


Further, it was by the FDA’s own deliberate decision that homeopathic drugs were excluded from former drug approval processes and intended to be a separate category. Venable continued:9


“The FDA deliberately excluded homeopathic drugs from both the Drug Efficacy Study Implementation (DESI) review (the process by which all drugs approved between 1938 and 1962 were retrospectively evaluated by the FDA for effectiveness) and the OTC Drug Review in 1972 (the process used to develop OTC drug monographs for allopathic drugs), deciding instead in the latter case to regulate homeopathic products separately because of their uniqueness.


By withdrawing the CPG and classifying all homeopathic drugs as unapproved drugs subject to FDA drug approval, the FDA is now requiring higher regulatory thresholds for OTC homeopathic drugs than are applicable to allopathic OTC drugs, many of which are permitted to be sold pursuant to the FDA monograph system. This move in effect penalizes an entire industry for the Agency’s 1972 decision.”


FTC Targeted Homeopathy in 2016


The FDA isn’t the first government agency to target this centuries’ old natural medicine system. In a notice filed in November 2016, the FTC stated that in order for homeopathic remedies to claim they are effective, their makers must provide proof. If no proof is provided, the remedies must state there is “no scientific evidence that the product works.”


In order to not mislead consumers, the FTC further stated that homeopathic remedies lacking sufficient proof must communicate to consumers that “the product’s claims are based only on theories of homeopathy from the 1700s that are not accepted by most modern medical experts.”10 Dana Ullman, MPH, CCH, one of the leading advocates for homeopathy in the U.S., said at the time:11


“Considering the longtime safety history of homeopathic medicines, it is surprising and even shocking that the FTC would consider proposing new regulations now.


One cannot help but wonder who or what is pulling their strings … policies … commonly result from powerful economic forces at play … it is clear that this governmental agency is ignoring important scientific evidence, and one must wonder if they are protecting Big Pharma from competition more than protecting the consumer.”


Does Homeopathy Work?


Based on the theory that “like cures like,” or the Law of Similars, homeopathy was founded by German physician Dr. Samuel Hahnemann. The idea is that health conditions can be healed by treating a person with minute doses of a substance that would produce similar symptoms to their health condition if given in larger doses.


Homeopathy’s other guiding principle is that of the minimum dose, which is based on the premise that the more a substance is diluted, the more potent homeopathic remedy it becomes, known as the “law of infinitesimals.” Homeopathic remedies may be made from plants, minerals or other substances and are commonly administered in pellet form, dissolved under the tongue. A number of intriguing studies suggest homeopathy is effective and safe for a variety of ailments, including flu. According to Ullman:


“The use of a homeopathic medicine called Oscillococcinum is an example of a remedy that can be effective for many people with the flu, though clinical experience suggests that it is most effective when used within 48 hours of getting flu symptoms. Although most homeopathic medicines are made from the plant or mineral kingdom, Oscillococcinum is unusual in that it is made from the heart and liver of a duck.”


In one study, nearly twice as many patients who were given Oscillococcinum recovered from the flu within 48 hours as those given a placebo.12 Further, Ullman noted:


A different group of researchers conducted a randomized, double-blind study involving 372 patients (188 treated with Oscillococcinum and 187 with placebo) of both sexes, ranging in age from 12 to 60, who presented rectal temperature ≥ 100.4 F, muscle pains, headache, or at least one of the following symptoms: shivering, chest pain, spine pain, coughing, irritation of nasal mucosa or feeling of malaise.13


Patients received three tubes of Oscillococcinum or placebo each day (morning, noon and night) for three days. The results of this trial show a highly statistically significant difference between the two groups, for what concerns disappearance of symptoms after 48 hours (19.2 percent in the Oscillococcinum group versus 17.1 percent in the placebo group) and improvement in symptoms (43.7 percent versus 38.6 percent for placebo).”


Additional research shows homeopathy’s promising role in the following conditions:

















In patients with allergies, those using homeopathy reported improvements in nasal airflow compared with a placebo group.

With homeopathic treatment, the researchers described a “clear, significant and clinically relevant improvement in nasal inspiratory peak flow, similar to that found with topical steroids.”14

Homeopathy significantly reduced the severity and duration of chemotherapy-induced stomatitis (swelling and sores in the mouth) in children.15
Homeopathic medicine was effective in treating acute childhood diarrhea, decreasing both the duration of the diarrhea and the number of stools per day.16,17Homeopathy has positive effects in children with attention deficit hyperactivity disorder (ADHD), particularly in the areas of behavioral and cognitive functions.18
Homeopathy lessened tender point pain and improved quality of life in people with fibromyalgia.19Homeopathic was effective in treating the early stages of vitiligo in a report of 14 cases20

FDA Continues to Crack Down on Natural Substances, Protect Big Pharma


The FDA’s new push to regulate homeopathic products is eerily reminiscent of their recent crackdown on the plant kratom. Leaves from the kratom tree have been used for pain relief for hundreds of years, but scientists now know they contain compounds that target the brain similarly to opioids, helping to relieve pain. It appears the plant may be safer than opioids for pain relief and could even act as a tool to help those suffering from opioid withdrawal.


In November 2017, however, rather than targeting the prescription opioids that are the root of the opioid epidemic, the FDA issued a public health advisory regarding risks associated with kratom use, suggesting that its usage could “expand the opioid epidemic.” What this comes down to, for some, is the right to choose what form of “medicine” to put in your body. As Dr. Lee Hieb, an orthopedic surgeon and past president of the Association of American Physicians and Surgeons, wrote in WND:21


“I’m not here to tout any particular over-the-counter remedy, but who gave the FDA total ability to limit what we can take into our bodies, while virtually forcing us to be given what they prescribe? It’s none of their business whether a ‘homeopathic remedy’ is worthless.


That’s an issue of commerce and truth in advertising. I, for one, want the freedom to research and decide for myself what supplements to take, even if my supplements ultimately do me no good. (Many do a great deal of good as Big Pharma knows only too well.)”


People have the right to choose their treatment, and doctors (many of whom admit to prescribing placebos to their patients) also retain the right to offer treatments they deem useful, whether it be homeopathy or another remedy.


As for the FDA’s new draft guidance on homeopathic drugs, it’s attempting to discredit such remedies’ proven healing powers before their mechanisms of action have even been fully understood. If you want to express your opinion on the matter, the FDA is accepting comments from the public until March 30, 2018.


– Sources and References 




The post All Homeopathic Products Now Illegal? appeared first on The Sleuth Journal.

Sunday, February 4, 2018

FDA Attacking The First Amendment: Is The Constitution Going Up In Vapor?

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Is The Constitution Going Up In Vapor?


According to the Pacific Legal Foundation, it most certainly is, literally.


PLF has filed a lawsuit against the unconstitutional Food and Drug Administration over what is being promoted as a healthy alternative to smoking.


It’s a product that has been sweeping the nation for a couple of years now, and it called vaping.


Part of the claim is that the FDA devised a rule against vaping that appears to clearly attack the First Amendment by regulating what can be said about a product, even if those claims are true.  Take a look at this short video.



According to PLF:


Electronic nicotine delivery systems—vaping devices and e-cigarettes—first hit U.S. stores in 2007. It didn’t take long for vaping to jump from zero to a $5 billion domestic industry, as entrepreneurs quickly recognized a market hungry for an alternative to traditional cigarettes.


In 2016, just as the burgeoning vaping industry was getting off the ground, the Food and Drug Administration (FDA) stepped in with a rule that deems e-cigarettes as tobacco products, and brand new, severe regulations that will only harm the industry and perhaps overall public health—contrary to the agency’s very mission.


Using a unique legal theory, Pacific Legal Foundation is suing the FDA in three separate federal courtrooms—at the same time—on behalf of vape store owners and a harm reduction organization in several states who want to promote a more healthy alternative to smoking.


The unconstitutional rule burdens these individuals and organizations in unique ways, but all are united in opposition to its continued enforcement.


The FDA’s regulations are not only expensive and onerous, and prevent vaping entrepreneurs from fulfilling what they believe is a humanitarian mission of helping people, but the rule was illegal the second it hit the Federal Register.


How in the world is a product that produces water vapor a tobacco product?  On what planet does that fly?  The same one that the same Communists tell us we are in the midst of global warming, over population and need a nanny state to tell us what to eat and drink.


It’s unconstitutional because only Congress has legislative authority under our Constitution.  Our Constitution doesn’t even mention an FDA, which has actually been the promoter of numerous drugs that have killed hundreds of thousands of peopleaccording to its own website.


Here’s where the cases are taking place.



  • In the U.S. District Court for the Northern District of Texas, PLF represents Joosie Vapes, owned by Denissa Moore and her husband, Larry Moore, Jr. Denissa used to smoke two packs a day, and tried to quit by using Chantix, nicotine patches, and even hypnosis. None of these were successful. She then turned to vaping and quit smoking after just a year. She founded Joosie Vapes with her husband in 2013 as a way to help others quit smoking.

  • In the U.S. District Court for the District of Minnesota, PLF represents five clients: Jen Hoban (pictured above), owner of Masterpiece Vapors, the Plume Room, J.H.T. Vape, Lakes Vape Supply, and Tobacco Harm Reduction 4 Life (THR4Life), a nonprofit organization.

  • In the U.S. District Court for the District of Columbia, PLF represents four businesses in three states:

    • Steve Green, owner of Mountain Vapors (California), was a 2+ pack a day smoker for 30 years who doctors warned was developing emphysema. A few years ago, his wife was given a vaping pen from a friend, which he tried and quit smoking that same day.

    • Kimberly Manor founded Moose Jooce in Michigan, after her late husband passed away from lung cancer.

    • PLF also represents Rustic Vapor in Michigan and Dutchman Vapors in North Dakota.




So, what is at stake in the case?



  • Rule-makers need to follow the rules: Under the Constitution, issuing regulations is the job of appointed officials who answer to the democratic process, not unelected career bureaucrats. This vaping rule was issued by such a bureaucrat in violation of the Constitution.

  • The vaping edict flouts the First Amendment by forcing businesses to run a daunting regulatory gauntlet in order to advertise truthful information. The government can’t require pre-approval for truthful speech, and it especially can’t shift the burden of proof to the speaker to prove the benefits of his speech will outweigh any harms the government perceives may result.

  • Beyond violating the Constitution, the vaping rule is horrible public policy: it threatens to shut down thousands of small businesses that provide potentially life-saving products and creates a public safety hazard by making it very difficult to improve and repair products.


Continued infringements of the rights of the people by those who take an oath to uphold the Constitution and at every turn violate that oath cannot continue to be tolerated in this country.  We have tolerated it too long.  It’s way past time to abolish the unconstitutional FDA as strong arm of the DC government.

Wednesday, January 31, 2018

‘90% Accuracy Rate’: New Artificial Intelligence Can Predict Your Death

AI Algorithms Predict Death

(ANTIMEDIA) — New deep learning algorithms, commonly referred to as artificial intelligence, are increasingly finding a home in the medical industry, where health care professionals are often overwhelmed. In palliative care centers, which include nursing and end of life care, an aging population has stretched medical and personnel resources to the limit, which just may mean this is the perfect time for AI to step in and help with both monitoring patients’ vital signs and making potentially life-saving prognoses.


The Food and Drug Administration (FDA) just approved the first algorithm that can monitor a patient in critical care and anticipate a life-threatening change in condition by up to 6 hours. The algorithm, called Wave Clinical Platform and developed by medical technology company ExcelMedical, is able to keep a 24/7 vigil over a patient, which is simply not possible for already overworked human care workers triaging in busy hospitals. The AI can also monitor patterns in vitals so as to determine whether, say, a sudden and simultaneous drop in oxygen saturation and a spike in blood pressure could be lethal.


Meanwhile, a research team at Stanford University is using an AI algorithm to predict patient mortality. A notoriously difficult task, predicting when a patient will die involves assessing a variety of factors from age and patient history to drug response and the illness itself. But it’s important to be as accurate as possible. Admitting a patient into end-of-life care too soon consumes valuable resources; admitting them too late risks leaving the patient cut off from their family.


Stanford’s AI has a 90% accuracy rate, which, according to some, is surprisingly and unsettlingly good. Created by feeding electronic health records (EHR) into a deep learning neural network, the AI is able to “sense” patient mortality within the next three to twelve months.


Jeremy Hsu of IEEE Spectrum described the model used as “an 18-layer Deep Neural Network that inputs the EHR data of a patient, and outputs the probability of death in the next 3-12 months.”


However, researchers admit they do not understand how the algorithm comes to its conclusion, a conundrum known as the “black box” problem. The Stanford team’s work is described in full detail in their paper, “Improving Palliative Care with Deep Learning.”


Ken Jung, a Stanford Medicine research scientist, and Anand Avati, whose team created the AI, hope the use of AI technology in medical environments could help with a number of problems, including palliative care and triage. Currently, while 80 percent of people say they want to die at home, only about 35 percent are able to. Employing new deep learning technology could enable better end of life care preparation and more personalized, consistent care once the patient is hospitalized.


That is, of course, if people can get past the stigma of having an advanced computer algorithm monitoring them when they’re ill.


Creative Commons / Anti-Media / Report a typo

Saturday, January 27, 2018

Sunday, December 31, 2017

Warning: The FDA’s Approval of Genome Therapy Is Just the Beginning

(ANTIMEDIA) — On Monday morning, the FDA announced the approval of a novel gene therapy for a rare inherited disease that affects vision in children and adults. This is a historic moment as it is the first time the FDA has approved a directly administered gene therapy for a specific gene mutation.


“Today’s approval marks another first in the field of gene therapy — both in how the therapy works and in expanding the use of gene therapy beyond the treatment of cancer to the treatment of vision loss — and this milestone reinforces the potential of this breakthrough approach in treating a wide-range of challenging diseases,” read the department’s press release.


Luxturna (voretigene neparvovec-rzyl) targets the RPE65 gene mutation associated with inherited retinal dystrophy. People who have a biallelic mutation, meaning mutation in both maternal and paternal copies of the RPE65 gene, aren’t able to produce an enzyme in the retina that converts light into an electrical signal transmitted to the brain, which leads to progressive vision loss, and ultimately blindness.


The gene therapy works by utilizing an existing virus as a vehicle to deliver a normal copy of the gene directly to the retina. This technique, called adeno-associated virus vector-based genome therapy, has gained traction as one of the most reliable forms of genome therapy. Still, there are some risks involved with using viral vectors, including the possibility of the virus targeting the wrong cells and causing other diseases, such as cancer.


Luxturna reports few adverse reactions (incidence ≥ 5%) in their official product insert, but they admittedly have yet to study the potential carcinogenesis effects of the therapy. In addition, the Phase 3 clinical trial of Luxturna was relatively small. It included 31 enrolled subjects, just 21 of whom actually received the treatment — barely above the minimum of subjects typically required for a Phase 1 trial, per official FDA guidelines.


Aside from the safety concerns of genome therapy, there are also numerous ethical concerns whenever genome editing is considered. As explained by the National Human Genome Research Institute, “…researchers and bioethicists are concerned that any genome editing, even for therapeutic uses, will start us on a slippery slope to using it for non-therapeutic and enhancement purposes, which many view as controversial.”


There is also the concern of the financial accessibility of the gene treatment. As NPR reported in October, analysts have speculated that the cost for each patient would be hundreds of thousands of dollars…for each eye. This means a cost of up to $1 million per patient, a price tag that begs a lot of questions about how the insurance industry will respond in terms of coverage and premiums in this previously uncharted territory of expensive gene therapy development.


Regardless of the causes for concern, the gene therapy industry is moving forward with no indication of stopping soon.


Spark Therapeutics of Philadelphia, the company behind Luxturna, is already in the early clinical stages of developing viral vector genome therapies for liver diseases and neurodegenerative diseases. The FDA is also moving forward with plans for further investment in genome therapy development in 2018, according to the same press release:


“Next year, we’ll begin issuing a suite of disease-specific guidance documents on the development of specific gene therapy products to lay out modern and more efficient parameters — including new clinical measures — for the evaluation and review of gene therapy for different high-priority diseases where the platform is being targeted.”


Whatever the case may be for the future of genome therapy, one thing is certain: this is just the beginning.


Creative Commons / Anti-Media / Report a typo

Friday, December 8, 2017

FOIA Docs Show FDA’s Data on Kratom Deaths is Complete Propaganda

kratomAs the FDA fearmongers over alleged Kratom associated deaths, documents on these deaths reveal that the American people are being lied to.

Friday, November 17, 2017

FDA Loyalty to Big Pharma Exposed in Move to Ban Plant that’s CURING Opioid Addiction

kratomThe FDA is now pushing to ban the highly beneficial plant kratom, which is curing opioid addiction. If we look deeper, we can see why they want it illegal.

Tuesday, November 14, 2017

FDA Approves New Digital Sensor To Ensure ‘Patients With Mental Health Issues’ Take Their Meds

digital-pill


The Food and Drug Administration has just approved a new pill with a digital sensor in it. It will “ensure” that patients who suffer from mental health issues take their medicine when they are told. But privacy concerns have not gone unnoticed.


Regulators in the United States have approved the first bill that can be digitally tracked as it makes its way through the human body.  The Abilify MyCite aripiprazole tablets used for treating schizophrenia and manic episodes have an ingestible sensor embedded inside them that records that the medication has been taken. A patch worn by the patient transmits this information to their smartphone.


But many are raising the red flag that this could simply be another form of medical “big brother.” You may no longer have the right to refuse medications in the very near future.


The Abilify MyCite features a sensor the size of a grain of sand made of silicon, copper, and magnesium. An electrical signal is activated when the sensor comes into contact with stomach acid — the sensor then passes through the body naturally. A patch the patient wears on their left rib cage receives the signal several minutes after the pill is ingested. The patch then sends data like the time the pill was taken and the dosage to a smartphone app over Bluetooth. The patch also records activity levels, sleeping patterns, steps taken, activity, and heart rate, and must be replaced every seven days. The patient’s doctor and up to four other people chosen by the patient, including family members, can access the information. The patient can revoke access at any time. – The Verge


Is it really hard to understand why people are raising concerns about privacy over this new pill? The pill is one way to address the prevalent problem of patients not taking their medication correctly. According to the IMS Institute’s estimates, the improper and unnecessary use of medicine cost the US healthcare sector over $200 billion in 2012.


But, the approval also opens the door for pills that are used for other conditions beyond mental health to be digitized and monitored, and could eventually lead to tracking devices for humans being slipped into medication. What is the government’s obsession with keeping the people doped up? Complacency, perhaps?


Others are worried that tracking pills will be a step towards punishing patients who don’t comply with either medical or government demands to take drugs. Ameet Sarpatwari, an instructor in medicine at Harvard Medical School told The New York Times the digital pill “has the potential to improve public health. [But] if used improperly, it could foster more mistrust instead of trust.”

Saturday, October 28, 2017

OxyContin Nation: Meet The Billionaire Family Who Helped Spark America"s Opiod Crisis

Via StockBoardAsset.com,


Unbeknownst to many, the Sackler Family, with assets of $13 billion, the nation’s 19th wealthiest family is one the top players in philanthropy. You can find the Sackler Gallery in the Smithsonian museum in Washington, D.C. or visit the Sackler wing at the Metropolitan Museum of Art in New York City. The Sackler’s even have a museum at Harvard, Guggenheim, and dozen of universities around the country. If it’s art— the Sackler family has it.


Participating in the art game takes money and a lot of it. So, where does the Sackler money come from?



According to Forbes, the “Sacklers continue to reap hundreds of millions of dollars in profits from the businesses in 2016– some $700 million last year, by Forbes’ calculations - from an estimated $3 billion in Purdue Pharma revenues plus at least $1.5 billion in sales from their foreign companies”.


Forbes outlines a brief history lesson of how the Sackler family got started in the world of medicine-




The family fortune began in 1952 when three doctors — Arthur (d. 1987), Mortimer (d. 2010) and Raymond Sackler — purchased Purdue, then a small and struggling New York drug manufacturer. The company spent decades selling products like earwax remover and laxatives before moving into pain medications by the late 1980s. To create OxyContin, Purdue married oxycodone, a generic painkiller, with a time-release mechanism to combat abuse by spreading the drug’s effects over a half-day.


 


The FDA approved the medication in 1995 and it soon took off. By 2003 OxyContin sales hit $1.6 billion as the drug helped drive a huge nationwide spike in opioid prescribing. At its peak in 2012, doctors wrote more than 282 million prescriptions for opioid painkillers, including OxyContin, Vicodin and Percocet  — nearly enough for every American to have a bottle.


 


Now opioid prescriptions are declining amid increased scrutiny over drug addiction, down 12% since 2012 according to data from healthcare information firm IMS Health. OxyContin (which is also beginning to face competition from authorized generics while fighting to protect its patents over tamper-proof, extended-release oxycodone) saw prescriptions fall 17%.  




It wasn’t until the 1980’s, as explained by Forbes, the Sackler family through their family-owned drug company called Purdue Pharma created OxyContin. Then in 1995, the FDA approved the medication and sales exploded. Sales hit $1.6 billion in 2003, as a nationwide spike in opioids was seen. By the peak in 2012, doctors wrote more than 282 million prescription for opioid painkillers, such as OxyContin, Vicodin and Percocet. Good times for the Sacklers from 1996- 2012, as the family drug business exploded.



According to The New Yorker, Oxycontin ” has reportedly generated some thirty-five billion dollars in revenue for Purdue” since 1995. OxyContin’s sole active ingredient is oxycodone, a chemical cousin of heroin, which makes it highly addictive.


The New Yorker further says Purdue used marketing techniques to deceive the American public of the drug’s true addictive characteristics.




Purdue launched OxyContin with a marketing campaign that attempted to counter this attitude and change the prescribing habits of doctors. The company funded research and paid doctors to make the case that concerns about opioid addiction were overblown, and that OxyContin could safely treat an ever-wider range of maladies. Sales representatives marketed OxyContin as a product “to start with and to stay with.” Millions of patients found the drug to be a vital salve for excruciating pain. But many others grew so hooked on it that, between doses, they experienced debilitating withdrawal.




Oddly enough, around the time OxyContin was approved, prescription opioid deaths across the United States surged. Fast forward to more relevant times, where heroin and fentanyl deaths are exploding.



Diving into the opioid crisis onto the streets of Baltimore. It’s very common to see local citizens shooting up heroin on city streets. In this video, I asked a man how did this addiction start? Guess what he said?... It all started with legal painkillers, such as OxyContin. 



As a few parasitical elites make billions flooding America’s streets with opioids. We the every day American citizen have to deal with the consequences, as President Trump outlined in yesterday’s opioid crisis speech:


  • In 2016, more than two million Americans had an addiction to prescription or illicit opioids.

  • Since 2000, over 300,000 Americans have died from overdoses involving opioids.

  • Drug overdoses are now the leading cause of injury death in the United States, outnumbering both traffic crashes and gun-related deaths.

  • In 2015, there were 52,404 drug overdose deaths — 33,091 of those deaths, almost two-thirds, involved the use of opioids.

  • The situation has only gotten worse, with drug overdose deaths in 2016 expected to exceed 64,000.

  • This represents a rate of 175 deaths a day.

Bottomline: It’s time for the American people to learn the truth about the opioid crisis and the very few elites who have profited. The question You should ask: why did our government allow this to happen?









Saturday, September 9, 2017

Some Journalists are Just Arsonists Pointing Fingers

Via The Daily Bell


Setting a fire is easier than putting one out.


And sometimes the people who fail to put out a fire are persecuted by the ones who don’t show up at all–or worse yet, fan the flames.


A recent Gizmodo article basically criticizes a volunteer fire department. No, not literally. This has nothing to do with actual fires of fire-fighters.


This has to do with an article called, “Some Crypto-Capitalists Just Want to See The World Burn.


Conspicuously lacking in the article is… how exactly the “crypto-capitalists” want to see the world burn?


The article tears apart all the ways the attendees of the Startup Societies Summit are trying to put out the fires of the world. It tries to torch innovative ideas about how to end poverty, clean up the environment, stop government abuse, feed the hungry, and advance modern medicine.


The author of the Gizmodo piece, Bryan Menegus, is like an arsonist saying, “awfully suspicious that every time there’s a fire, all these firefighters are on the scene…”


If Menegus had a superpower, it would be the uncanny ability to find nefarious motivations for even the most innocuous solutions to serious problems.


Summoning his powers, he first cherry picks two sentences from a 15-minute presentation on how to solve the refugee crisis using Special Economic Zones (SEZs).



Among the most extreme examples of expanding SEZs was Michael Castle Miller’s presentation on “refugee cities”—a proposal to turn refugee camps into their own Shenzhens. “We can actually convert refugees into economic assets that drive us towards the economic and social progress we want to achieve,” he says. Through one lens it gives those stuck in political limbo a semblance of normalcy; through another it sees immigration as a problem in need of solving and turns refugee camps into company towns running off the labor of the displaced. “It’s an investment opportunity because now all of a sudden there’s a huge labor force out there of untapped skills that nobody else can access.”



Maybe in the utopia in Menegus’ mind, immigration is not a problem in need of solving. But in the real world, millions sit in camps not allowed to work for their own economic benefit.


Apparently, governments setting up camps and then funding them without end fits into the Savior Complex of Gizmodo and associates. Instead of freeing and empowering individuals, they think of people as weak, in need of constant nurturing by mother government. Yet these refugees are being smothered by their matriarchal providers. Governments don’t let them work and refuse to let them integrate into economies surrounding the encampments.


You might think allowing someone the opportunity to work and provide for themselves and their families would be a good thing. All Menegus sees is exploitation. Somehow, he casts company towns as worse than the literal prisons in which refugees now live.


When he wants to criticize, Menegus has no difficulty conjuring up images of a burning world, ripe for greedy capitalists to take advantage of desperate victims in need.


Yet all these troubles evaporate when he questions the suspicious actions of the event’s speakers.



When asked what he’s running from that requires a man-made island on the ocean, Joe Quirk says “pretty much all the governments that exist.”



Menegus had countless examples of how the naive attendees, refugees, the poor, and others would be taken advantage of by greedy capitalists. But suddenly the scary world in need of government protection disappears. What’s so bad that you need to run?


I don’t feel like rehashing the genocides, wars, exploitation, nor the racial, gender, and religious discrimination perpetrated by various governments. From Jim Crow laws to Ruby Ridge, from the Tuskegee experiments to torture at Gitmo, there is plenty to run from in reference to the U.S. government alone.


But also, why ignore the failures? The failure of the government to end poverty, the failure to solve crime, the failure to restore the environment, heal the sick, and so much more?


As much as Quirk runs from the psychopaths in government, he tackles the problems they have never been able–or willing–to solve. I suppose Menegus would just have us wait for our saviors to get around to rescuing us poor helpless souls.


But the people involved in Startup Societies prefer to take matters into their own hands.


Let’s Talk About Failure


Don’t all the people at this conference know how many times these ideas have failed, the article suggests.


If only we could all be like Edison, The Wright Brothers, and Einstein, who all got the lightbulb, the airplane, and the theory of relativity right on their first try.


Of course, failure alone does not mean you will eventually succeed. But Menegus has to ignore the mountains of evidence in order to pretend the projects discussed have no future.


And ignore the data, or twist it, is exactly what he does.



The hope, for those like Strong, is that these experiments will not only alleviate global poverty, but show otherwise oppressive nations a better way forward—a concrete oasis that paves a path to more liberalized future governance—but it’s unclear if that’s been the case in any of the dozens of countries currently hosting an SEZ. If wages and conditions improve in one zone, what prevents corporations from packing up and finding a new crop of foreign bodies to run the machines?



It’s only unclear if you haven’t bothered to look into it.


Read another way, here is what Menegus is actually asking:


A special economic zone could improve the lives of workers and residents so much that companies no longer have cheap labor in the SEZ. Now that their former workers have the economic freedom to choose other options, what’s to stop a company from finding new crops of foreign bodies to lift out of poverty with the same methods?


Imagine the horror! What if these companies just bop around the world creating wealth, and empowering individuals until there is no one left to exploit!? Then who will Gizmodo and Bryan Menegus save with their snarky articles and sassy critique?


Relevant comparisons are ripe for analysis.


Why do South Koreans live in a normal wealthy nation, while North Koreans have not advanced since the two countries split? Before the Korean War, the populations were equally matched economically.


What’s the difference between China and Hong Kong that makes Hong Kong one of the wealthiest places on Earth? What about Singapore’s rapid development after their independence in the 1960’s?


Joe Quirk’s book Seasteading: How Floating Nations Will Restore the Environment, Enrich the Poor, Cure the Sick, and Liberate Humanity from Politicians, highlights how experimenting with government could lift people out of poverty, solve overcrowding in cities, feed the masses while reducing the environmental impact of farming.


And yet he is likened to snake-oil salesmen. Menegus doesn’t miss the opportunity to take a shot at Quirk’s hair–which I think is lovely–and “frat boy” attitude.


Ironically, some of these experiments that Menegus is so quick to torch as libertarian fantasies, are not very libertarian at all.


Sure, economically speaking Singapore is very free. But Joe Quirk points out in his book that it also has universal health care and an annual government budget surplus. On the other hand Singapore has no minimum wage and 2% unemployment.


Hong Kong requires no licenses for any business. They also boast “no sales tax, no capital gains tax, no goods and services tax, no value added tax, no annual net worth tax, no inheritance tax, and no estate tax.”


Yet 50% of the residents of Hong Kong live in a form of subsidized housing and every resident receives free emergency medical care. The top 8% of Hong Kong residents shoulder 60% of the tax burden, and the bottom 60% of residents pay no income taxes.


So why is Menegus so quick to rule out these projects, when some of them resemble the progressive dream?


Quirk’s point is not that progressives are wrong and libertarians are right. He says “While the West argued, the East experimented.” There simply have not been enough modern experiments in government to yield any concrete data. We need more experiments. 


No Thanks, I’ll Take My Business Elsewhere


Menegus dismisses one of the clearest signs that the “exitarian” strategy is viable.


Peter Thiel helped found the Seasteading Institute. Among other things, they promote the idea of islands or ships hosting medical tourism offshores from restrictive or expensive countries.



Offshore medical research is something Thiel is already engaged in, and which has been described as “patently unethical.”



What the Menegus refers to is the testing of a herpes vaccine. You know, the thus far incurable virus.


Instead of being thwarted by the costs and bureaucracy of the FDA, or waiting 20 years and hoping the “valley of death” doesn’t scare off investors, Thiel took action.


So some shmucks connected to the U.S. government call it unethical. Big surprise.


Volunteers with herpes are getting a chance to be cured, without having to wait 20 years for the FDA to–maybe–approve it. What’s so unethical about skirting an agency known to be corrupt, which derives a big chunk of its revenue from being paid off by pharmaceutical companies?


In truth, Menegus’ Gizmodo article reads like a Newsweek article from 1995 triumphantly declaring the internet would never catch on.


This is, of course, laughable now. In a few years, it will be laughable to think we should have continued another 1,000 years of government identical to the last 1,000 years of government.


Startup Societies are primed to revolutionize the way government works. Singapore, Hong Kong, countless special economic zones, and even innovative cruise lines stand as clear signs of times to come for anyone paying attention.


In 1995, the internet was sometimes more hassle than it was worth. It didn’t do any of its functions particularly well. There was still a lot of experimentation needed to flesh out the proper applications.


Twenty-two years later, it is hard to imagine the world without it.


Everyone has an Agenda


I don’t want to be misleading here. The event organizer, Joe McKinney, who Menegus trashes in the opening of his article, is a friend of mine. I don’t like to see my friends maligned, especially when they are working their asses off to seriously improve the world. And yes, that is going to make me somewhat biased.


But the idea that Menegus is a neutral journalist is laughable. He, and Gizmodo, have an agenda.


They promote the idea of helplessness. They sell a victim mentality. If someone’s making money, someone else must be getting screwed. If someone aligns with a particular political agenda, then everything else they say should be ignored.


Of course, their political beliefs are altruistic and legitimate. They are just trying to fight Nazi’s and help the poor. But when Joe Quirk talks about how to help the poor, he’s just a used car salesman trying to make a buck.


Menegus assumes the worst of any business and assumes government has the best intentions. But people are people. Some are motivated by greed, and others by altruism, regardless of whether they join the government or the private sector.


But you can disengage from businesses. Menegus didn’t have to be at the Summit, and he doesn’t have to join any Startup Society. No one does.


Yet all 7.5 billion people on Earth must choose between 195 countries. And in reality, most of them can’t choose to leave or enter any particular country at will.


All the Startup Society Foundation is saying is that we should have more options. Let’s get more experiments going, and we can see what type of government works the best.


Menegus can start or join one with a universal basic income and censorship if he wants.


The people at the Startup Society Summit are looking for peaceful solutions. Yes, some of them want to exit, and no longer consort with the type of people who read Gizmodo. How crazy to want to disengage from people who say things like:



These people are so entrenched in a helpless victim mindset, they can’t think of any way to solve simple problems of security without government. But they do highlight the biggest threat which faces Startup Societies: violent governments enabled by angry, hateful voters.


Why exactly do these people want to see everyone with differing views murdered by terrorists and governments?


Other commenters were quick to point out the similarities of Startup Societies to the video game Bioshock. The attendees of the event preferred history and science to inform their comparisons.


But the best comment has got to be this one:



I feel that we would get a lot more realistic and useful tech and vision from these people if we shipped them to a government-free island for a few years. Then when they come back they should have at least a basic understanding of what the government is here for, for better or worse, and how to get what they need they will need to work within the current system because it’s not possible to just exclude themselves and create another – they are wholly dependent on it.



This comment reveals the clear misunderstanding between the Startup Societies project and the uninformed critics.


First, the people involved in Startup Societies are attempting to put themselves on “islands” without traditional government. They are begging to not be attacked by governments for simply trying out their own forms of governance. If the critics aren’t afraid of the results, why are they so violently opposed to the experiment?


Second, the Startup Societies may be critical of typical government, but they aren’t opposed to any governing structure whatsoever. Every project proposes mechanisms for how to govern the territory. It is just that the methods of rule-setting don’t involve coercion, theft, and violence.


The truth is they would never come back from the island. But plenty of people would be begging to come join–just like in Singapore and Hong Kong.


This won’t be the last hit piece on Startup Societies as the ideas catch on. But who cares? The whole point is to disengage from people who want to control us, who thinly veil their violent aggression with altruistic excuses a Savior Complex.