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Trump’s FDA Is Bringing Back Asbestos and Making Russian Company Very Happy

In his continued effort to make America great again, Donald Trump is bringing back asbestos.

Asbestos is a mineral fiber with a lot of qualities desirable for manufacturing. It’s an excellent heat insulator, it dampens sound, and it is fire-resistant, strong, and inexpensive. It also causes cancer. Many studies have confirmed it.

It also causes cancer. Asbestos exposure is the only known cause of mesothelioma, a deadly form of lung cancer that is known to be extremely painful. Asbestos exposure is also linked to other lung diseases. Many studies have confirmed this. Thousands of lawsuits have been won against asbestos companies. In the last thirty years, seventy billion dollars has been spent on asbestos litigation, and more than seventy companies have been driven into bankruptcy because of said litigation. The Environmental Working Group estimates that 12,000 to 15,000 people die yearly in the U.S. from asbestos exposure, but other studies indicate that asbestos could be responsible for 40,000 deaths per year in the U.S. If you find asbestos in your home the EPA strongly recommends that you hire a professional to remove the asbestos. They come in with hazmat suits and respirators.  More than 60 countries have banned the use of asbestos. In the U.S. Here, the EPA only banned some uses of the material but all uses.

Despite all of this, Trump likes asbestos.

There is no new research disputing the health effects of asbestos, but regardless, Trump’s EPA wants to expand the legal uses for Asbestos. Can you guess why? One hint. Russia.

Uralasbest, a Russian mining firm, placed a seal with Trump’s face on their asbestos products. On their Facebook page, they posted their appreciation:

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Дональд на нашей стороне!Комбинат «Ураласбест» выпустил необычную партию хризотила: на упаковке паллетов с минералом…

Posted by ОАО "Ураласбест" on Sunday, June 24, 2018

The translation reads:

Donald is on our side!

The combine “Uralasbest” produced an unusual batch of chrysotile: on the packaging of pallets with a mineral there is a stamp

“Approved by Donald Trump, 45th President of the United States”. In this unusual way, the workers of the combine’s asbestos-processing plant thanked US President Donald Trump for his words in defense of chrysotile-asbestos.

He supported the head of the US Environmental Protection Agency Scott Pruitt, who stated that his agency would no longer deal with the negative effects that could potentially result from products containing asbestos. Donald Trump supported the specialist and called asbestos “100 percent safe after use.”

“We came out with the initiative to support our chrysotile industry in this way and remind that our” mountain flax “is an important mineral for the whole world. The management has approved! “, They told in the factory.

The EPA declined to ban uses of asbestos that have already been abandoned by industry. They also put forth a “significant new use rule,” or SNUR, that requires manufacturers to notify and seek approval from the EPA before resuming asbestos production and uses.

According to environmental advocates, this new rule gives chemical companies the upper hand in creating new uses for such harmful products in the United States. In May, the EPA released a report detailing its new framework for evaluating the risk of its top prioritized substances. The report states that the agency will no longer consider the effect or presence of substances in the air, ground, or water in its risk assessments.” – The Architects Newspaper

The EPA is ignoring specific exposures to asbestos in the safety assessments, which is reportedly in violation of law, and they are disregarding the safety risks from asbestos that still lingers in old schools, homes, and building materials just about everywhere in the U.S.

The EPA has also eliminated many kinds of asbestos from the FDA’s definition of asbestos.

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Being Overweight at a Young Age Linked To Changes In Adults’ Heart

Overweight people are at a higher risk of developing high blood pressure and cardiovascular disease, regardless of their age, a new study from the University of Bristol in the U.K. says. Researchers chose to concentrate on the Body Mass Index (BMI) and routinely collected cardiovascular data from young adults aged 17 and 21. Dr. Kaitlin Wade, lead author of the study, says,

Our results suggested that having a higher BMI likely causes higher blood pressure…These findings suggest that BMI is likely to have an adverse causal impact on cardiac structure even in young adults…Our results support efforts to reduce BMI to within a normal, healthy range from a young age to prevent later cardiovascular disease.”

Healthy or Healthier

A healthy BMI is considered to be between 18.5 and 24.9, and the average American (male and female) is objectively overweight at 26.5. This study found a definite link between higher BMI and incidences of high blood pressure in young adults. It also found that a high BMI correlated to other cardiovascular anomalies, even in study participants that were considered otherwise healthy.

Related: Cayenne and Capsaicin, Natures Miracle Medicine

Healthy 17-year-olds with a high BMI were more likely to have an enlarged left ventricle, which develops when the heart’s main pumping chamber has to work harder than normal. This can be due to high blood pressure or a response to a larger body needing a greater volume of blood. The muscle can eventually lose its elasticity and subsequently the ability to pump enough blood.  That can later lead to an irregular heartbeat, stroke, or sudden cardiac arrest.

The Other Factors

So how does this happen? Why are healthy seventeen-year-olds experiencing cardiovascular symptoms more traditionally found in older people?

The 1970s ushered in an era of intense focus on the risk factors surrounding heart diseases such as smoking, “unhealthy” diet, or untreated high blood pressure. They also coincided with the rise of new medications like beta-blockers to treat these issues. These measures resulted in fewer deaths from heart disease and were treated as successes. Meanwhile, the causes of heart disease weren’t necessarily addressed, and in some instances were even swept under the rug. For example, the Sugar Research Foundation discovered that sucrose offset rodent metabolisms, increasing their levels of triglycerides. This leads to clogged arteries and increases a person’s predisposition to cardiovascular disease.

Today’s young person is dealing with an entirely new set of risk factors, the majority of them related to diet. Every single one of the people in this study has been eating or exposed to GMOs since birth, the first generation to claim that dubious honor. They’re also suffered through the modern world’s incredibly confusing relationship with fat. McDonald’s, for example, switched their fry oil from beef tallow to soy-corn oil the year after the subjects for this review were born. Increased agricultural chemicals, plastics of dubious health, and more medicated childhoods are only some of the other factors to examine when trying to diagnose why 17-year-olds are experiencing poor health before their time.

Related: Popular Antibiotics May Increase Susceptibility to Serious Heart Condition

New Discoveries

We predict the number of studies discovering young people experiencing health conditions previously associated with old people will only increase. There are quite a few happening now, and a rise in cancer and heart disease among the next generation is here. The single most important thing we can teach our children is how to eat truly healthy, exercise, and take care of themselves.

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Monsanto Lost! Ordered to Pay $289 million in California Roundup Cancer Trial

Today (Friday, August 10th) a California jury found Monsanto liable for causing cancer and ordered the company to pay $289 million in damages. The jury at San Francisco’s Superior Court of California deliberated for three days. The lawsuit was filed by Dewayne Johnson, who alleges that the company’s glyphosate-based weed-killers, including Roundup, are responsible for his cancer.

Johnson’s doctors testified that he is probably not going to live past 2020. Johnson is 46. He worked for a California county school system where he reportedly applied the weed killer up to 30 times per year for pest-control.

This was the first lawsuit to make it to trial that alleges that glyphosate does cause cancer. Monsanto was recently bought by Bayer AG for $65 billion. The German conglomerate faces more than 5,000 similar lawsuits in the United States.

Related: How to Avoid GMOs in 2018 – And Everything Else You Should Know About Genetic Engineering

The jury awarded Dewayne Johnson $39 million in compensatory damages and $250 million in punitive damages. Dwayne was diagnosed with non-Hodgkin’s lymphoma in October of 2014, and with a “more aggressive form of the cancer” in March 2015.

Monsanto says that decades of scientific studies have shown glyphosate, the world’s most widely used herbicide, to be safe for human use. But studies, including a brand new one, show otherwise:

Exposure to environmentally relevant doses of a glyphosate-based herbicide during pregnancy has been found not only to impair female fertility in rats…Argentinian researchers tested the glyphosate-based herbicide – one commonly used in Argentina – in pregnant female rats at two doses, which were added to their food. The rats were mated and dosed from the 9th day after conception until their pups were weaned. This first generation of offspring and their offspring in turn (second generation) were followed and monitored for reproductive effects.”

Johnson’s case was filed in 2016. The case was fast-tracked for trial due to the severity of his cancer.

FILE PHOTO: Plaintiff Dewayne Johnson listens as attorney Brent Wisner (out of frame) speaks about his condition during the Monsanto trial in San Francisco, California, U.S., July 09, 2018. Josh Edelson/Pool via Reuters/File Photo




Meat and Dairy Industry On Course To Contribute More Global pollution Than OIL Companies

Within the next few decades, Big Meat and Big Dairy will surpass Big Oil for climate pollution, according to a new study by the non-profits GRAIN and the Institute for Agriculture and Trade Policy. The jointly published study quantified emissions from 35 of the world’s largest meat and dairy companies.

The non-profit researches analyzed 35 of the meat and dairy industry’s biggest companies. The researchers warned that meat and dairy companies will overtake oil firms as the world’s biggest polluters. The authors of the study say that factory meat and dairy farms are ‘majorly overlooked climate culprits.

Related: How to Avoid GMOs in 2018 – And Everything Else You Should Know About Genetic Engineering

According to the report, the five largest meat and dairy corporations—JBS, Tyson, Cargill, Dairy Farmers of America, and Fonterra—are already responsible for more annual greenhouse gas emissions than ExxonMobil, Shell, or BP.

They also found that businesses did a poor job reporting their emissions and targets, and many failed to report emissions entirely or excluded supply chain figures, which amount to 80 to 90 percent of total emissions.

Watch the video below to see how the meat industry could actually help reduce climate change.

Related: Stop Eating Like That and Start Eating Like This – Your Guide to Homeostasis Through Diet

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FDA Loophole That Allows Farmers To Administer Antibiotics Indefinitely

Antibiotics benefit farmers by speeding up the time it takes livestock to be ready for slaughter. Cows and chickens and other livestock grow faster with antibiotic use than they would otherwise. For cattle, the time from birth to slaughter can be cut in half. But antibiotic resistance is a growing public health concern.  Antibiotic-resistant bacteria like e.coli can be pathogenic to humans and even deadly. Farm water runoff and animal waste are damaging our ecosystems in a myriad of ways. Consequently, in 2017 the FDA was compelled to act.

The C.D.C. states that 23,000 Americans die each year due to antibiotic-resistant bacterial infections and they estimate that more than 400,000 United States residents become ill with infections caused by antibiotic-resistant food-borne bacteria every year. They believe that one in five of these antibiotic-resistant infections may be caused by pathogens from food and animals.

Recommended: Best Supplements To Kill Candida and Everything Else You Ever Wanted To Know About Fungal Infections

In 2017, the Food and Drug Administration enacted rules that prohibited antibiotics from being used for growth promotion in livestock. Previously these antibiotics could be purchased over the counter but the new rules require a prescription from a veterinarian.

Despite the ban, it’s widely believed that ranchers still use antibiotics to speed growth. The F.D.A. rules have a glaring loophole: farmers can use antibiotics for disease prevention.

You don’t even need a sick animal in the herd to use antibiotics in the feed and water as long as the justification is ‘disease prevention’ not ‘growth promotion,’ ” Avinash Kar, a senior attorney at the Natural Resources Defense Council

Courtesy of the CDDEP

More in-depth reading: Antibiotics in Meat Could Be Damaging Our Guts & New Report Tracks Rise of Antibiotic Resistance in Humans and Livestock

Our health depends on our gut’s ecosystem. Antibiotics, vaccinations, glyphosate, and GMOs are known to disrupt the bacteria in our gut. If you eat meat, we recommend careful consideration regarding who your buy meat from.

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Trump Administration Ordered to Stop Drugging Migrant Children

The Shiloh Treatment Center, in Texas near Manvel, is one of 32 Texas facilities that is licensed to care for migrant children who have been separated from their parents. The officials there were administering psychotropic prescription drugs to migrant children without consent from the parents. This violates the state’s child welfare laws. Late last month U.S. District Judge Dolly Gee in Los Angeles ordered that the Trump administration must stop giving these drugs to migrant children without parental or guardian consent, except in an emergency.

The federal judge also ordered that the government move the children out of that facility except for children that were deemed to pose a “risk of harm.”

Government officials said they only provided the psychotropic on an emergency basis, but the judge didn’t believe it, and pointed to testimony from children who said they were drugged “every morning and every night.” Children testified that U.S. Office of Refugee Resettlement staff members would sometimes refuse to tell the children what drugs they were taking or why. Some reported being forcibly injected. Children said they experienced side effects including nausea, dizziness, depression, and weight gain.

One child held at Shiloh identified as Isabella said,

“I witnessed staff members forcefully give medication four times.

. . . Two staff members pinned down the girl . . . and a doctor gave her one or two injections.”

Recommended: In Shocking Development, Chemicals in Food and Packaging are Toxic to Children

Read more: Trump administration must stop giving psychotropic drugs to migrant children without consent, judge rules




In Shocking Development, Chemicals in Food and Packaging are Toxic to Children

The American Academy of Pediatrics recently issued a statement calling for more stringent food safety standards. Children are especially vulnerable to the negative effects of food additives, processed foods, and toxic food packaging. These harmful substances can have long-lasting health consequences for little ones. The chemicals of particular interest to the AAP are nitrates, bisphenols, phthalates, and perfluorinated compounds. In spite of a growing number of scientific studies, the FDA still lists these products as “generally regarded as safe” (GRAS). The AAP wants to change, or at least reexamine, that.

Regulation and oversight of many food additives is inadequate because of several key problems in the Federal Food, Drug, and Cosmetic Act. Current requirements for a “generally recognized as safe” (GRAS) designation are insufficient to ensure the safety of food additives and do not contain sufficient protections against conflict of interest. Additionally, the FDA does not have adequate authority to acquire data on chemicals on the market or reassess their safety for human health. These are critical weaknesses in the current regulatory system for food additives. Data about health effects of food additives on infants and children are limited or missing; however, in general, infants and children are more vulnerable to chemical exposures.”

“Safe” Chemicals to Look Out For

The health problems with generally regarded as safe chemicals are fairly well known, although the way in which they affect children in the long-term is not definitively known. Nitrates/nitrite, phthalates, bisphenols (including bisphenol A (BPA), bisphenol AF (BPAF), bisphenol Z (BPZ), bisphenol S (BPS), bisphenol F (BPF), bisphenol AP (BPAP), and bisphenol B (BPB), and perfluorinated compounds (PFCs) are ever present in today’s food system, and they can be found both in and around the items we feed our children.

Related: How to Detox From Plastics and Other Endocrine Disruptors
  • Nitrates, which turn into nitrites, are ions that naturally occur in a wide range of foods like celery, spinach, lettuce, onions, broccoli, and peas. They perform a useful function in the body, acting as a free radical, and an argument can successfully be made that nitrates are safe. However, they are able to function positively in vegetables because vitamin c and polyphenols in the plants keep carcinogenic n-nitroso compounds from forming. Nitrates used as preservatives processed animal-based products like hot dogs and lunch meats produce a very different effect on health, as they don’t have the same polyphenols and antioxidants and allow n-nitroso to form. Those compounds have been linked to cancer, mania (mental health issues), and can render hemoglobin unable to carry oxygen. This is an example of a substance that is beneficial in one context and a serious health risk in another. A proper vetting process from a regulatory agency would be able to notice the difference.
  • PFCs come into contact with food through grease, oil, and stain resistant coating on food wrappers. They are also used in Teflon and can be found in non-stick cookware. This is a large group of chemicals and some of the more recognizable compounds are perfluorooctane sulfonate (PFOS), perfluorooctanoic acid (PFOA), perchlorates, and perfluoroalkyl. Researchers have found connections between these chemicals and endocrine disruption, kidney and testicular cancer, liver toxicity, immune system damage, and most immediately relevant to children, reduced birth weights. It takes three years for any amount of PFCs that enter the body to reduce to half. There are children who have had a non-necessary chemical linked to numerous health conditions in their systems since they were born.
  • Bisphenols are commonly used in cans, bottles, and receipts. Trace amounts of these chemicals are also found in drinking water throughout the U.S. These chemicals are endocrine disruptors and have been linked to hormonal issues; breast, prostate, and testicular cancers; and inflammatory bowel disease. The most famous of the bisphenols is bisphenol-A (BPA), which incidentally the FDA banned the use of in baby bottles in 2012. They did allow the GRAS designation to continue for the rest of the bisphenols, but a recent study has found that those chemicals cause hormonal issues like BPA does. Some of them (BFAP, BPB, and BPZ) are even better at mimicking estrogen in the body, the primary reason for bisphenols’ endocrine disruption. The New York State Assembly recently proposed a bill expanding the ban on BPA in children’s bottles to a ban on all bisphenols. No word yet from the FDA, though.
  • Phthalates are added to plastics to make them more flexible and are found in water pipes, electronics, medical devices, food packaging, and a myriad of other places. There are many of them and no way to avoid them. Even the most scrupulous avoidance practices (glass packaging, organic, filtered water…) will be unable to completely filter them out and their GRAS status (which does not require their presence to be announced) ensures they can be anywhere. Some of the more prominent phthalates are fat-soluble, making foods containing high levels of fat like dairy and meat a likely culprit of exposure. Phthalates have been linked to endocrine disruption and breast cancer, as well as other conditions like asthma, attention-deficit hyperactivity disorder, diabetes, autism, and neurodevelopmental disorders.

This is not new information. But we need to ask why this is the best our food system can do. The AAP is continuing that discussion, and the question remains. Why are these chemicals still “generally regarded as safe”?

Related: Sugar Leads to Depression – World’s First Trial Proves Gut and Brain are Linked (Protocol Included)

How We Got Here

The GRAS designation was introduced in 1958. The list was meant to be used only for staples like salt and pepper, but an amendment to the law in 1997 gave companies the power to make their own decisions on which ingredients are generally regarded as safe. The rule also made the reporting process for these decisions entirely voluntary. That rule has not been significantly modified since 1997. Changes were published in 2016, but those didn’t address what become a major health issue, companies allowed to market products they have decided are safe without any actual government oversight or independent scientific review. In the FDA’s own words in 2016,

We also are amending our regulations to replace the voluntary GRAS affirmation petition process with a voluntary notification procedure under which any person may notify us of a conclusion that a substance is GRAS under the conditions of its intended use.”

If we are to believe the FDA, we’ve moved to a system where the administration has even less oversight. No longer are companies required to ask for permission. Now they merely tell us it’s safe based on the numbers and studies they themselves have produced. This is a system ripe for corruption.

It’s also a system that hasn’t significantly changed or made accommodations for how quickly food technology is changing. All of the above substances, nitrates, phthalates, PFCs, and bisphenol are still regarded as safe, in spite of multiple studies claiming otherwise. The FDA has a major conflict between what independent science has discovered, and the AAP is not the only organization to highlight that fact. Several prominent consumer and environmental groups, including Center for Food Safety, Breast Cancer Prevention Partners, Center for Science in the Public Interest, Environmental Defense Fund, and the Environmental Working Group, sued the administration in 2017 for failing to do its job.

Now we have a major medical group that serves one of the most vulnerable groups in the U.S., children, calling for change. Which is great, but the FDA has received this kind of admonishment before.

Related: Autism Correlates with Circumcision

This Parent’s Rant

How does it make you feel as a parent?

I feel demoralized. The amount of judgment involved in raising a child is overwhelming.

I’m angry. Sometimes it feels like even those who are trying to help aren’t actually doing anything. The FDA isn’t. According to Dr. Leonardo Trasande, the lead author of the statement and chief of the division of environmental pediatrics at New York University’s School of Medicine,

The good news is there are safe and simple steps people can take right now to limit exposures, and they don’t have to break the bank…”

Why is that my job now? Of course, I want to ensure that my little ones are as healthy and free from dangerous chemicals as possible. But why is the health of my kids and your kids and the kids you never see in your neighborhood because they can’t go anywhere without supervision less important than a company being able to label their products with toxic plastic hardeners the way they always have? Why am I the one to bear those costs? I know it’s naive to assume it’s that simple, but it doesn’t make me any less angry.

As a mother, I can’t help seeing how quickly we are condemned for stepping even a little out of line. Telling your child they can’t have ice cream in the grocery store results in people who have no knowledge of your food needs telling you to let the kid have a treat. Allowing children to run and play in public spaces, even parks, produces contempt from complete strangers. Let’s not even touch on how quickly parents who dare to question vaccinations are shamed.

Why doesn’t that exist for the companies that systematically undermine our health and food systems when they know how much damage they’re causing? It’s money, and there’s no way I can compete. I’m demoralized, and sometimes it’s too much.

Our priorities as a country are incredibly disappointing and more damaging than we can fully appreciate. Lately, I find myself wondering what would happen if the companies that knowingly deny how toxic their chemicals are and prevent further study to maximize profits were punished as swiftly as a woman leaving her 8-year-old child in the car to get coffee.

Related: New Study Shows Glyphosate Does Cause Tumors and Birth Defects, and More

Does It Have to Be This Way?

The AAP is correct to call out the FDA for the GRAS designations. The FDA is meant to regulate food safety. Yet companies have the ability to put products are on the shelf with ingredients that have received no impartial or independent scrutiny. At some point, every consumer has to put their trust in someone to produce food for them. The FDA has lost that trust.

These chemicals fundamentally alter the quality of life that is available to our children. The body is always detoxing, but how can that be effective when these chemicals are constantly being replenished? The health challenges to overcome for our next generation continue to accumulate. This needs to be addressed sooner, rather than later.

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