Cashews Are A Natural Anti-Depressant


Two handfuls of cashews is the therapeutic equivalent of a prescription dose of Prozac. Inside you, the essential amino acid L-tryptophan is broken down into anxiety-reducing, snooze-inducing niacin. Even more important, tryptophan is also made into serotonin, one of your body’s most important neurotransmitters. Serotonin gives a feeling of well-being and mellowness, or as the Australians would say, “no worries.” This is such a profound effect that Prozac, Paxil and similar antidepressants usually either mimic serotonin or artificially keep the body’s own serotonin levels high. You can do the same thing with your food. And no one can tell us that beans, peas, cheese, nuts and wheat germ are toxic if you eat a lot of them! Plenty of carbohydrates (starches) in your meals help tryptophan get to where it does the most good: in your brain. In order to cross the blood-brain barrier to get in, carbos are required. So cheese and crackers provides a better effect than the cheese standing alone. An egg or two on toast is better than just the egg. Beans, peas, and nuts already contain carbohydrate, so you are all set there. Consider that five servings of beans, a few portions of peanut butter, or just one big handful of cashews provides one to two thousand milligrams of tryptophan, which will work as well as prescription antidepressants… but don’t tell the drug companies. Some skeptics think that the pharmaceutical people already know. Here are two quotes in evidence: “Pay careful attention to what is happening with dietary supplements in the legislative arena… If these efforts are successful, there could be created a class of products to compete with approved drugs. The establishment of a separate regulatory category for supplements could undercut exclusivity rights enjoyed by the holders of approved drug applications.” (Source: FDA Deputy Commissioner for Policy David Adams, at the Drug Information Association Annual Meeting, July 12, 1993) Here are 15 other Amazing Health Benefits Of Cashew Nuts Who doesn’t know about cashew nuts? Caju is what we call them in India. We use them mostly in sweets and children love to eat them as they are. They are full of anti-oxidants, vitamins and minerals which are required for the normal functioning of the body. They actually belong to Brazil but Portuguese brought them to India in the 16th century. The kidney shaped or bean shaped nuts have many health benefits, a few of which are presented below: 1. Prevents Cancer: Proanthocyanidins are a class of flavonols which fight against tumor cells by stopping them to divide further. These proanthocyanidins and high copper content in cashew nuts help fight against cancerous cells and keeps you away from colon cancer. This is one of the major cashew nut benefits. 2. Healthy Heart: Cashews contain low fat content when compared to other nuts and that too in the oleic acid form which is very healthy for heart. They are cholesterol free and the antioxidants present keeps you away from heart diseases. 3. Lowers High Blood Pressure: Cashew nuts lower your blood pressure with the help of magnesium present in them. 4. Helps Hair: Copper is the mineral which helps your hair get that color. So if you take cashews which are full of copper content, you can get that black hair that you always wished for. 5. Healthy Bones: Like calcium, magnesium is also important for bone health which is the main content in cashew nuts. 6. Healthy Nerves: Magnesium is stored on the bones surface which prevents calcium from entering the nerve cells and thus keeps the blood vessels and muscles relaxed. Insufficient amount of magnesium can lead calcium to enter the blood vessels leading them to contract. It also leads to high blood pressure, migraine headache etc. 7. Prevents Gallstones: Daily intake of cashewnut can reduce the risk of developing gallstones up to 25%. 8. Helps in Weight Loss: Even though cashew nuts are considered as fats, it contains good cholesterol. So contrary to popular belief, those who eat cashews at least twice a week gain less weight when compared to those who eat less. 9. Anti-oxidants: Selenium, copper, magnesium etc. act as co-factors for many enzymes. 10. Helps Digestion: Cashew nuts help in growth and development, nucleic acid synthesis and digestion. 11. High on Vitamins: Cashew nuts are rich in vitamins like riboflavin, pantothenic acid, thiamin, niacin etc. These vitamins keep you safe from sideroblastic anemia, pellagra, etc. 12. Healthy Gums and Teeth: As mentioned before, the magnesium content present in cashew nuts is very good for bones. So it gives healthy teeth as well as strong gums to hold them. 13. Pleasant sleep: After menopause, these cashew nuts can give you relaxed and pleasant sleep during nights. 14. Free Radicals: Cashew nuts help our body to utilize iron properly and eliminate free radicals which cause health problems. 15. Macular Degeneration: Cashew nuts have the ability to filter Sun’s UV rays and protect us from macular degeneration. Now that you know the health benefits of Cashew nuts, ensure that you eat a few once every week I am sure you already love them.

 

Four elements earn permanent seats on the periodic table


The seventh row of the periodic table is officially full.

periodic table

On December 30, the International Union of Pure and Applied Chemistry announced that a Russian-U.S. collaboration had attained sufficient evidence to claim the discovery of elements 115, 117 and 118. IUPAC awarded credit for the discovery of element 113 to scientists at RIKEN in Wako, Japan (SN Online: 9/27/12). Both groups synthesized the elements by slamming lighter nuclei into each other and tracking the decay of the radioactive superheavy elements that followed.

Researchers at the Joint Institute for Nuclear Research in Dubna, Russia, and Lawrence Livermore National Laboratory in California, which are among the institutions credited with elements 115, 117 and 118, had also laid claim to element 113 after experiments in 2004 (SN: 2/7/04, p. 84) and 2007. But garnering recognition for the three other elements softened the blow, says Dawn Shaughnessy, who leads the experimental nuclear and radiochemistry group at Livermore. “I’m personally very happy with IUPAC’s decision,” she says.

Published reports on the newly recognized elements will appear in early 2016, says IUPAC executive director Lynn Soby. Official recognition of the elements means that their discoverers earn the right to suggest names and symbols. Element 113 will be the first element discovered and named by researchers in Asia.

Brain activity is as unique as fingerprints, and correlates to intelligence, study finds


Coming soon: job interviews by brain scan?

A person’s behaviour and way of doing things can often give them away to those who know them best, and now research says it’s not just our outward idiosyncrasies that can identify us – even our brain activity is unique.

Researchers at Yale University in the US have found that images of brain activity taken by functional magnetic resonance imaging (fMRI) can be used as a kind of ‘cognitive fingerprint’ to identify particular individuals – and can even correlate to how intelligent we are.

“In most past studies, fMRI data have been used to draw contrasts between, say, patients and healthy controls,” said Emily Finn, co-first author of the study. “We have learned a lot from these sorts of studies, but they tend to obscure individual differences which may be important.”

And those differences can be telling. So telling, in fact, that when the researchers analysed numerous fMRI scans taken of 126 participants sourced by the Human Connectome Project, they were able to identify individuals by recognising their unique ‘connectivity profile’.

The researchers looked at activity across some 268 different regions in the brain by scanning the participants six times over. Sometimes the researchers engaged the participants with a cognitive task during the fMRI scan, while during other sessions, they simply rested during the procedure.

The researchers were able to identify individual participants with up to 99 percent accuracy when comparing scans of the same person involved in a similar cognitive task, although their strike rate fell to about 80 percent if the scan showed the same person doing a disparate task or being at rest.

“Until this, we really didn’t know the extent to which each unique individual has a unique pattern of connectivity,” Russell Poldrack, a cognitive neuroscientist at Stanford University and advisor to the Human Connectome Project, told Rachel Ehrenberg at Nature.

And beyond simply identifying who you are, the study also shows that brain activity can give researchers clues about a person’s level of intelligence. While fMRI data doesn’t simply indicate how smart you are, connectivity patterns in brain activity do correlate to how well people perform in an intelligence test, according to the researchers.

“[T]he uniqueness seems to be tied to cognitive function in some way,” said Poldrack, with stronger connections in participants’ prefrontal and parietal lobes correlating to better intelligence test scores.

While some might worry that these kinds of techniques could potentially be used for discriminatory purposes in the future – the prospect of having to undergo a mandatory brain scan as part of the interview process for a job or college position, for example – what excites the researchers is the potential for brain activity data to be used for therapeutic purposes, where treatments could be specifically tailored to an individual’s unique brain connectivity profile.

“We have hundreds of drugs for treating neuropsychiatric illness, but there’s still a lot of trial and error and failed treatments,” Finn told Nature. “This might be another tool.”

Gene-editing technique successfully stops progression of Duchenne muscular dystrophy


Using a new gene-editing technique, a team of scientists from UT Southwestern Medical Center stopped progression of Duchenne muscular dystrophy (DMD) in young mice.

If efficiently and safely scaled up in DMD patients, this technique could lead to one of the first successful -based treatments for this fatal disease, researchers said.

DMD, the most common and severe form of muscular dystrophy among boys, is characterized by progressive muscle degeneration and weakness. It is caused by mutations in the X-linked DMD gene that encodes the protein dystrophin. The disease affects one in 3,500 to 5,000 boys, according to the Centers for Disease Control and Prevention and other estimates, and often leads to premature death by the early 30s.

Although the genetic cause of DMD has been known for nearly 30 years, no effective treatments exist. The disease breaks down muscle fibers and replaces them with fibrous or fatty tissue, causing the muscle to gradually weaken. This condition often results in heart muscle disease, or cardiomyopathy, the leading cause of death in these patients.

In the study published today in Science, UTSW researchers used a gene-editing approach to permanently correct the DMD mutation that causes the disease in young mice.

“This is different from other therapeutic approaches, because it eliminates the cause of the disease,” said senior author Dr. Eric Olson, Chairman of Molecular Biology, and Co-Director of the Senator Paul D. Wellstone Muscular Dystrophy Cooperative Research Center at UT Southwestern.

In 2014, Dr. Olson’s team first used this technique – called CRISPR/Cas9-mediated genome editing – to correct the mutation in the germ line of mice and prevent muscular dystrophy. This paved the way for novel genome editing-based therapeutics in DMD. It also raised several challenges for clinical applications of gene editing. Since germ line editing is not feasible in humans, strategies would need to be developed to deliver gene-editing components to postnatal tissues.

To test this out, researchers delivered gene-editing components to the mice via adeno-associated virus 9 (AAV9). DMD mice treated with this technique produced dystrophin protein and progressively showed improved structure and function of skeletal muscle and heart.

“AAV9 can efficiently infect humans in a tissue-specific manner, but it does not cause human disease or toxicity. It’s a molecular missile for gene therapy,” said Dr. Leonela Amoasii, a postdoctoral researcher in the Olson lab and co-lead author of the study with Dr. Chengzu Long, Instructor of Molecular Biology.

“The CRISPR/Cas9 system is an adaptive immune system of single-celled organisms against invading virus. Ironically, this system was hijacked, we packaged it into a nonpathogenic virus, and corrected a genetic mutation in an animal model,” added Dr. Long.

The CRISPR genome-editing technology, which was developed by a researcher at University of California at Berkeley, was picked as the “Breakthrough of the Year” scientific development by Science.

“This study represents a very important translational application of genome editing of DMD mutations in young mice. It’s a solid step toward a practical cure for DMD,” said Dr. Rhonda Bassel-Duby, Professor of Molecular Biology and Co-Principal Investigator of a genomic editing project with Dr. Olson at the Wellstone Center.

“Importantly, in principle, the same strategy can be applied to numerous types of mutations within the human DMD patients,” added Dr. Olson, who also serves as Director of the Hamon Center for Regenerative Science and Medicine, and holds the Annie and Willie Nelson Professorship in Stem Cell Research, the Pogue Distinguished Chair in Research on Cardiac Birth Defects, and the Robert A. Welch Distinguished Chair in Science.

Now, the research team is working to apply this gene-editing technique to cells from DMD patients and in larger preclinical animal models.

This marks the first major finding of the UTSW Wellstone Center, which was recently established with $7.8 million in funding from the National Institutes of Health. UTSW is one of six Wellstone Centers across the country, which work to translate scientific findings and technological developments into novel treatments for muscular dystrophy, and to promote basic, translational, and clinical research. UT Southwestern’s Wellstone Center focuses on Duchenne .

“The recent groundbreaking discoveries from the Olson laboratory using genome editing to correct the genetic mutation that causes DMD have accelerated the race to find a cure for this deadly disease,” said Dr. Pradeep Mammen, Associate Professor of Internal Medicine and Co-Director of the UTSW Wellstone Center. “The challenge now lies before Wellstone Center researchers to translate these discoveries in the mouse model of DMD into a therapy for patients with DMD.”

Members of the UT Southwestern team whose research successfully halted progression of a form of muscular dystrophy in mice included (l-r) Dr. Chengzu Long, Dr. Eric Olson, Dr. Rhonda Bassel-Duby, Dr. Leonela Amoasii, John Shelton, and Alex Mireault. Credit: UT Southwestern Medical Center

Using a new gene-editing technique, a team of scientists from UT Southwestern Medical Center stopped progression of Duchenne muscular dystrophy (DMD) in young mice.

If efficiently and safely scaled up in DMD patients, this technique could lead to one of the first successful -based treatments for this fatal disease, researchers said.

DMD, the most common and severe form of muscular dystrophy among boys, is characterized by progressive muscle degeneration and weakness. It is caused by mutations in the X-linked DMD gene that encodes the protein dystrophin. The disease affects one in 3,500 to 5,000 boys, according to the Centers for Disease Control and Prevention and other estimates, and often leads to premature death by the early 30s.

Although the genetic cause of DMD has been known for nearly 30 years, no effective treatments exist. The disease breaks down muscle fibers and replaces them with fibrous or fatty tissue, causing the muscle to gradually weaken. This condition often results in heart muscle disease, or cardiomyopathy, the leading cause of death in these patients.

In the study published today in Science, UTSW researchers used a gene-editing approach to permanently correct the DMD mutation that causes the disease in young mice.

“This is different from other therapeutic approaches, because it eliminates the cause of the disease,” said senior author Dr. Eric Olson, Chairman of Molecular Biology, and Co-Director of the Senator Paul D. Wellstone Muscular Dystrophy Cooperative Research Center at UT Southwestern.

In 2014, Dr. Olson’s team first used this technique – called CRISPR/Cas9-mediated genome editing – to correct the mutation in the germ line of mice and prevent muscular dystrophy. This paved the way for novel genome editing-based therapeutics in DMD. It also raised several challenges for clinical applications of gene editing. Since germ line editing is not feasible in humans, strategies would need to be developed to deliver gene-editing components to postnatal tissues.

To test this out, researchers delivered gene-editing components to the mice via adeno-associated virus 9 (AAV9). DMD mice treated with this technique produced dystrophin protein and progressively showed improved structure and function of skeletal muscle and heart.

“AAV9 can efficiently infect humans in a tissue-specific manner, but it does not cause human disease or toxicity. It’s a molecular missile for gene therapy,” said Dr. Leonela Amoasii, a postdoctoral researcher in the Olson lab and co-lead author of the study with Dr. Chengzu Long, Instructor of Molecular Biology.

“The CRISPR/Cas9 system is an adaptive immune system of single-celled organisms against invading virus. Ironically, this system was hijacked, we packaged it into a nonpathogenic virus, and corrected a genetic mutation in an animal model,” added Dr. Long.

The CRISPR genome-editing technology, which was developed by a researcher at University of California at Berkeley, was picked as the “Breakthrough of the Year” scientific development by Science.

“This study represents a very important translational application of genome editing of DMD mutations in young mice. It’s a solid step toward a practical cure for DMD,” said Dr. Rhonda Bassel-Duby, Professor of Molecular Biology and Co-Principal Investigator of a genomic editing project with Dr. Olson at the Wellstone Center.

“Importantly, in principle, the same strategy can be applied to numerous types of mutations within the human DMD patients,” added Dr. Olson, who also serves as Director of the Hamon Center for Regenerative Science and Medicine, and holds the Annie and Willie Nelson Professorship in Stem Cell Research, the Pogue Distinguished Chair in Research on Cardiac Birth Defects, and the Robert A. Welch Distinguished Chair in Science.

Now, the research team is working to apply this gene-editing technique to cells from DMD patients and in larger preclinical animal models.

This marks the first major finding of the UTSW Wellstone Center, which was recently established with $7.8 million in funding from the National Institutes of Health. UTSW is one of six Wellstone Centers across the country, which work to translate scientific findings and technological developments into novel treatments for muscular dystrophy, and to promote basic, translational, and clinical research. UT Southwestern’s Wellstone Center focuses on Duchenne .

“The recent groundbreaking discoveries from the Olson laboratory using genome editing to correct the genetic mutation that causes DMD have accelerated the race to find a cure for this deadly disease,” said Dr. Pradeep Mammen, Associate Professor of Internal Medicine and Co-Director of the UTSW Wellstone Center. “The challenge now lies before Wellstone Center researchers to translate these discoveries in the mouse model of DMD into a therapy for patients with DMD.”

Vaccine fraud exposed: Measles and mumps making a huge comeback because vaccines are designed to fail, say Merck virologists


Disclaimer: I am not an opponent of the theory of inoculation. Nor am I opposed to science. What I am opposed to is fraudulent science, and that’s what this article is all about.

Measles and mumps are making a huge comeback in the United States, but doctors and journalists all make the same critical error in understanding why. They blame “parents who don’t vaccinate their kids” as the cause, but the real cause — as revealed by whistleblowing scientists working for top vaccine manufacturers — is that measles and mumps vaccines are designed to fail from the start.

Scientific fraud, it turns out, is an inherent part of the vaccine industry.

How do we know? Because whistleblowers who worked in the industry have found the courage to speak out and tell the truth. These people are the Edward Snowdens of the vaccine industry.

Merck falsified its mumps vaccine efficacy results, say former employees

Merck knowingly falsified its mumps vaccine test results to fabricate a “95% efficacy rate” say former Merck virologists Stephen Krahling and Joan Wlochowski in their shocking False Claims Act document.

As I wrote last year, ” In order to do this, Merck spiked the blood test with animal antibodies in order to artificially inflate the appearance of immune system antibodies.”

From the False Claims Act complaint:

Merck also added animal antibodies to blood samples to achieve more favorable test results, though it knew that the human immune system would never produce such antibodies, and that the antibodies created a laboratory testing scenario that “did not in any way correspond to, correlate with, or represent real life … virus neutralization in vaccinated people,” according to the complaint.

Merck, of course, denies the claims, just like all the drug companies deny ever engaging in bribery, or using children for medical experiments, or ghostwriting “scientific” studies that get published in science journals, or conspiring to suppress competing generic drugs and so on. Yet, as history has shown, all the top drug companies are routinely engaged in widespread criminal behavior, including conspiracy, fraud, bribery and more.

Stephen Krahling and Joan Wlochowski are simply telling us what we already suspected: that Merck falsifies the efficacy of their vaccines in order to make them appear to be working when they actually aren’t. Why would a drug company do such a thing? Consider the fact that Merck has both motive and opportunity.

Why drug companies design vaccines to fail

The vaccination dogma is so deeply embedded in the minds of doctors, journalists and the public, that any time a communicable disease starts to spread, everybody immediately leaps to the false conclusion that “more vaccines are needed.” This is very nearly a Pavlovian reaction in the minds of the brainwashed masses. “Spread of disease = lack of vaccines.”

Thus, the spread of disease actually boosts vaccine sales. Epidemics are a “marketing tool” to create demand for a profitable product that people can be convinced to purchase over and over again, year after year, whether it works or not.

And how do you create that demand? You engineer an epidemic by making sure your own vaccine products don’t work. Fear drives people to get vaccinated, so fear is used as the primary marketing tool.

But why hasn’t the con been exposed yet? Why haven’t scientists announced that most of the children afflicted with measles and mumps are the very same children who were vaccinated? One study showed that 97 percent of children afflicted with mumps had already been vaccinated against mumps.

In 2010, a mumps outbreak spread in New Jersey, and 77 percent of children afflicted with mumps had already been vaccinated against mumps.

The same is true with measles. Most measles outbreaks spread among those who have been vaccinated against measles.

When a swine flu outbreak swept through Britain in 2010, it turns out that 70 percent of those infected had already been vaccinated against swine flu.

Far from protecting people from disease outbreaks, vaccines often promote the pandemic they claim to prevent.

Vaccines are ASSUMED to work, not proven to work

Why does the industry keep getting away with this fraud? The answer is because nobody ever compares infection rates of vaccinated vs. unvaccinated people. They all just ASSUME vaccines work because that is the dogma of modern medicine. Assumption becomes “fact” in the minds of brainwashed medical experts.

This is one of the tenants of the fraud-based medical system: Vaccines are assumed to work 100% of the time, without exception, and anyone who questions this is immediately branded a heretic. There is no tolerance whatsoever for any critical thinking or scientific inquiry when it comes to vaccines. And God forbid if you bring up the issue of mercury in vaccines, as the vaccine industry apparently believes that mercury magically becomes non-toxic when used in vaccines and injected into the body.

Thus, vaccines that fail (due to low efficacy) are never detected or even questioned. The fraud continues right under our noses. So a vaccine company can easily put a mumps or measles vaccine into circulation that is designed to fail while actually weakening the immune system from the mercury, formaldehyde, MSG and aluminum that are still used in vaccines today.

This actually causes an increase in the spread of these diseases, resulting in more alarmist media stories about the “spread of measles and mumps” which then results in more parents rushing to CVS pharmacies to get their children injected with yet another useless vaccine.

How’s that for an insidious profit model?

But it’s even worse than that. While some vaccines are simply designed to fail, other vaccines are designed to cause outbreaks of disease.

Some vaccines are actively spiked with live viruses to cause pandemics

As Natural News previously exposed, the vaccine industry was caught shipping live viruses to vaccine manufacturers of flu vaccines in 18 countries.

This was done by none other than Baxter International, Inc. one of the top suppliers of “weakened” flu virus material for use in vaccines. Except in this case, they weren’t weakened. Vaccines made with this material simply gave people the flu!

In the realm of desktop computing, many people believe that anti-virus companies write and release viruses in order to cause fear and boost demand for their products. It’s an incredibly effective way to sell more products. All you have to do is pay a group of hackers a couple of million dollars to keep writing viruses that get covered in the mainstream media. The scarier the story, the more people buy anti-virus software. I happen to know firsthand that McAfee uses dishonest scare tactics to sell their security software services, claiming your website is infected when it actually isn’t.

Vaccine companies, it turns out, use the same tactic. From time to time, they allow live viruses into the flu shots, thereby spreading influenza and causing the very kind of fear and panic that drives people into pharmacies to buy more vaccines.

The WHO and CDC are all part of it too, stirring up irrational fear and panic like they did with the H5N1 virus a few years ago. It turns out that WHO panel members receive kickbacks from drug companies to engineer these anti-science scare stories.

During the swine flu pandemic, it was revealed that 5 of the 15 members of a WHO advisory panel had financial ties to the very same drug companies who would financially benefit from the pandemic. That’s called “conflict of interest” in any other industry, yet for some reason it is fully tolerated in the fraudulent vaccine industry.

In 2010, an outstanding article by Dr. Gary Null explained much of this in excruciating detail. Read that article here on Natural News.

The deeper you dig into the vaccine industry and its longstanding practice of scientific fraud, misrepresentation, fear mongering and “medical false flags,” the more you realize just what a total con the vaccine industry has become.

Learn more: http://www.naturalnews.com/042864_measles_outbreak_mumps_vaccines_scientific_fraud.html#ixzz3w70mss7L

Apple Cider Vinegar – One Of The Most Powerful Health Tonics In Your Kitchen


8 Reasons Apple Cider Vinegar Is One Of The Most Powerful Health Tonics In Your Kitchen

 

The question is not what Apple Cider Vinegar can do, but what can’t it do. As a folk remedy, it has been credited with curing everything from the flu to warts or sunburn to dandruff. However, it also can help reverse many serious diseases that many would immediately turn to pharmaceutical medications to solve.

The benefits of apple cider vinegar come from it’s healing compounds which include acetic acid, potassium, magnesium, probiotics and enzymes. Science has verified this through empirical evidence observed through the ages.

Apple cider vinegar can kill head lice, ease digestion, prevent flu, prevent acne, reduce inflammation, kill fungus, regulate pH balance, dissolve kidney stones and helps relieve allergies, migraines, asthma, nausea, heart burn and wash toxins from the body.

Here are 7 more reasons apple cider vinegar is one of the most powerful health tonic in your kitchen.

7 Reasons To Use Apple Cider Vinegar

1) Diabetes.

The effect of apple cider vinegar on blood sugar levels is perhaps the best researched and the most promising of its health benefits. Several studies have found that vinegar may help lower glucose levels. For instance, a study (White, A. Diabetes Care, November 2007) of 11 people with type 2 diabetes found that taking two tablespoons of apple cider vinegar before bed lowered glucose levels in the morning by 4%-6%. In another study from Arizona State University, subjects took a drink of 20 grams of apple cider vinegar and 40 grams of water. Those with insulin resistance who drank the vinegar had 34% lower postprandial (after-meal) glucose compared to controls.

Vinegar may be the most cost-effective diabetes medicine in history, but most people with diabetes still aren’t aware of its benefits.

2) Allergies

This miracle vinegar helps to break up mucous throughout the body and cleanse the lymph nodes. Believe it or not, research suggests that apple cider vinegar can help with allergies because of its ability to reduce mucous and sinus congestion. When reducing the effects of allergies, it can also help stave off sinus infections and their related symptoms, such as sore throats and headaches.

3) High Cholesterol.

A 2006 study reported in Medscape General Medicine, showed evidence that ACV could lower cholesterol. In a study published in a foreign medical journal, scientists found an apple cider vinegar-enhanced diet may increase HDL (“good” cholesterol) and reduce levels of triglycerides, while research in rats also suggests that apple-cider vinegar can help control triglycerides and cholesterol (Journal of Agricultural and Food Chemistry, June 22, 2011).

4) Blood Pressure and Heart Health.

A large observational study found that people who ate oil and vinegar dressing on salads five to six times a week had lower rates of heart disease than people who didn’t. Researchers have suggested that ‘this reduction in blood pressure may be caused by the significant reduction in renin activity and the subsequent decrease in angiotensin II’. Potassium in the vinegar ‘balances sodium levels in the body, which aids in maintaining blood pressure within healthy limits’ and ‘apple cider vinegar also contains magnesium, a mineral that works to relax blood vessel walls and thus lower high blood pressure’. Another study in rats also found that vinegar could lower high blood pressure.

5) Restores Acid/Alkaline Balance

Apple cider vinegar helps the body maintain a healthy alkaline pH level, and some ‘alternative’ practitioners recommend using apple cider vinegar to help balance the body’s alkaline/acid levels. The theory behind the alkaline diet is that our blood is slightly alkaline (with a normal pH level of between 7.35 and 7.45) and that our diet should reflect this pH level as the body constantly strives to achieve this state of equilibrium.

Research shows that higher acid levels (lower pH level) leads to a lack of energy and higher incidences of infection. Proponents of the alkaline-acid theory believe that a diet high in acid-producing foods leads to lack of energy, excessive mucous production, infections, anxiety, irritability, headache, sore throat, nasal and sinus congestion, allergic reactions, and increased risk of conditions such as arthritis and gout.

6) Face and Hair Health

It is widely known that apple cider vinegar can be used as a rinse for your hair after shampooing to add healthy body and shine. Recycle an old shampoo bottle and fill it with 1/2 a tablespoon of apple cider vinegar and a cup of cold water. Pour through your hair after shampooing several times a week.

You can also dilute apple cider vinegar with two parts water, and spread the concoction over your face with a cotton ball as a toner at night after washing, or in the morning before you apply your moisturizer. You can also dab apple cider vinegar directly onto age spots and leave them on overnight to lighten their color.

7) Weight Loss.

For thousands of years, vinegar has been used for weight loss. Why? White vinegar (and perhaps other types) might help people feel full. A study (Ostman, E. European Journal of Clinical Nutrition,2005) of 12 people found that those who ate a piece of bread along with small amounts of vinegar felt fuller and more satisfied than those who just ate the bread.

A 2009 study on mice showed that consuming acetic acid (the active component in ACV), upregulates the expression of genes for fatty acid oxidation enzymes in the liver causing a suppression in body fat accumulation. In a double-blind experiment, obese Japanese were assigned to three different groups based on similar body weights, body mass indexes (BMI), and waist circumference. Each group drank a 500 ml drink containing either 30ml, 15ml, or 0ml of vinegar daily for 12 weeks. Those in the 30ml and 15ml groups had lower BMI, visceral fat area, waist circumference, serum triglyceride, and body weight to the control group of 0ml. The 12-week weight losses were modest: 1.2kg in the 15ml group and 1.7kg in the 30ml group. These two groups consumed a similar number of calories to the control group and also performed a similar amount of exercise, so the effect is not likely to have been due to an impact on appetite or other lifestyle changes. It was concluded that consumption of vinegar might reduce obesity.

Final Note.

Unpasteurized or organic Apple Cider Vinegar (ACV) contains mother of vinegar, which has a cobweb-like appearance and can make the vinegar look slightly congealed. It’s the best way apple cider vinegar should be consumed.

Nine Dangers of Fluoride Exposure


Exposure to fluoride is a contentious topic, mostly because exposure is everywhere. Not only is fluoride acommon ingredient in toothpaste, many municipalities have a fluoridated water supply. Why? Well, the reason we’re given is that it encourages oral health… even though it’s not known to prevent harmful oral bacteria. [1] What is known is that fluoride is toxic. In fact, the number one reason for poison control calls concerning fluoride are for children who’ve eaten toothpaste. [2] [3] Long-term ingestion is harmful to the brain, digestive system, heart, bones… even the tooth enamel it’s supposed to help. [4] [5] [6] These next 9 shocking facts will make you take a second look at your exposure to fluoride.

fluoride-small

1. Weakens Skeletal Health

Skeletal fluorosis is a condition resulting from fluoride consumption. The liver is unable to process fluoride, thus it passes into the bloodstream where it combines with calcium that’s been leeched from the skeletal system. You’re left with weak bones, otherwise known as skeletal fluorosis. The risk has been known about for decades yet it’s not been established how much exposure will trigger skeletal fluorosis… and the impact it has on quality of life is horrendous. [7] [8] [9] The best way to protect yourself is to avoid fluoride. Recently, Chinese authorities established a link between reductions in fluoride exposure and the incidence of fluorosis. [10]

2. Causes Arthritis

Fluoride has been shown to cause calcification of cartilage, the essential tissue for joint health. [11] Degenerative osteoarthritis has been linked to skeletal fluorosis. [12] And in a study of individuals suffering from fluorosis,osteoarthritis knee conditions occurred frequently. [13]

3. Toxic to the Thyroid

Iodine and fluoride belong to a family of compounds known as halogens. Although iodine is beneficial to the thyroid, fluoride is not. However, because of the similarities, the thyroid can absorb fluoride instead of iodine. This is bad. Fluoride is toxic to thyroid cells; it inhibits function and causes cell death. [14] For decades, fluoride was used to reduce thyroid function in individuals suffering from an overactive thyroid. [15] Now — and pay attention to this — the range used in water fluoridation matches the levels typically used to reduce thyroid function. [16]

4. Calcifies the Ultra-Important Pineal Gland

Although the full capabilities of the pineal gland have been the subject of debate for centuries, it’s known for certain that, at a minimum, the pineal gland regulates body rhythms and wake-sleep cycles; two extremely important functions. Fluoride is especially toxic to the pineal gland, where it accumulates and calcifies the gland. In fact, by the time the average person reaches old age, their pineal gland will have higher calcium density than their bones. [17]

5. Accelerates Female Puberty

It also deserves mention that the pineal gland plays an integral role in the onset of puberty. Research has shown that girls living in areas prone to more fluoride exposure experience puberty earlier than girls exposed to less. [18] Fluoride’s damaging effect on sexual functiononly begins here…

6. Harmful to Male and Female Fertility

A direct link exists between fertility rates and fluoridated drinking water. Higher levels of fluoride correspond to lower fertility rates, particularly with drinking water levels of 3 ppm. [19] Animal models show that fluoride reduces reproductive hormones in females. [20] Men have it just as bad; those suffering from fluorosis have lower testosterone and fertility than men with limited fluoride exposure. [21]

7. Bad for Kidney Health

Fluoride is toxic to the kidneys and a higher rate of chronic kidney disease has been reported in areas where the water contains high levels of fluoride. [22] [23] According to Chinese researchers, a fluoride level of 2 mg/L is all it takes to cause renal damage in children. [24]While water fluoridation levels are often much lower than this, the fluoride bombardment continues with toothpaste and other sources.

8. Harmful to the Cardiovascular System

Research suggests that exposure to fluoride causes cardiovascular inflammation and atherosclerosis. [25] [26] Other research has examined its effect on blood pressure but had mixed results. Regardless, despite that cardiovascular disease can have many causes, the evidence, and history show its incidence increases with exposure to fluoride.

9. Negative Cognitive Effects

The Fluoride Action Network reports that, as of May 2013, 43 studies have examined the effect of fluoride on human intelligence. The results should motivate anyone to minimize their fluoride exposure. One observation is that fluoride negatively impacts children’s neural development. [27] Another is that children living in highly fluoridated areas have up to five times greater chance of developing a low IQ compared to those who do not. [28]

Reducing Your Exposure to Fluoride

Using non-fluoride toothpaste can immediately reduce your fluoride exposure. Maintaininghealthy iodine levels can help protect the thyroid from fluoride. Fluoridated water is the largest concern and most water filters are not adequate for removing fluoride; instead look to a reverse osmosis water purification systems.

Have you made efforts to reduce your exposure and minimize the dangers of fluoride? What tips do you have? Please leave a comment below and share with us.

How an orgasm a day can slash a man’s cancer risk


  • Men who ejaculate more frequently lower their risk of the disease
  • Those who ejaculate 21 times a month or more cut their risk by 22%
  • This was compared to men who ejaculated up to 7 times a month
  • Theorists say orgasm flushes out cancer-causing chemicals and old cells

Men who have regular orgasms – once a day – are less likely to be diagnosed with prostate cancer, a study has found.

Regular ejaculation throughout their lives reduces the risk of the disease, scientists discovered.

The researchers, from Harvard Medical School, said they could not explain why orgasms could lower prostate cancer risk, adding further research is necessary.

However it has previously been suggested that regular orgasms may flush out cancer-causing chemicals in the prostate.

Men who ejaculate more frequently throughout their lives lower their risk of prostate cancer, a study found

Another theory is that if sperm is regularly cleaned out to allow new cells to develop, it helps stop the build-up of old cells that might be more likely to turn cancerous.

The prostate is a small satsuma-sized gland located between a man’s penis and his bladder.

Its main function is to produce a thick white fluid that is mixed with the sperm produced by the testicles, to create semen.

The Harvard study is the largest to date to examine the frequency of ejaculation and related prostate cancer risk.

The researchers found that men in the 40 to 49 age bracket who ejaculate 21 or more times a month reduced their risk of prostate cancer by 22 per cent.

This was compared to men who ejaculate four to seven times a month.

MEN WHO SLEEP WITH MULTIPLE WOMEN ‘REDUCE THEIR RISK OF PROSTATE CANCER ‘

To protect against prostate cancer, take a lover – or 20.

According to a study, men who sleep with multiple women are almost a third less likely to develop the disease.

Researchers at the University of Montreal found men who have more than 20 notches on their bedpost slashed their risk of prostate cancer by 28 per cent.

And the study also revealed that men who have slept with more than 20 women reduced their chances of getting the most aggressive tumours by 19 per cent.

Celibacy, on the other hand, doubles the risk of the disease.

The research was published in the journal Cancer Epidemiology.

While the researchers said they were unclear as to why ejaculation lowers the chances of prostate cancer, they called the results ‘particularly encouraging’.

The study followed almost 32,000 healthy men for 18 years – 3,839 of whom later were diagnosed with prostate cancer.

Men were asked about their average monthly frequency of ejaculation between the ages of 20 to 29, 40 to 49, and in 1991, the year prior to the questionnaire.

They found that the more frequently a man ejaculated throughout his life, the lower his risk of prostate cancer at all three of these points in time.

This was the case even when they adjusted their results to take factors such as diet, lifestyle and a history of prostate cancer screening into account.

Dr Jennifer Rider, of Harvard Medical School and Brigham and Women’s Hospital, said the results are ‘particularly encouraging’ but should be interpreted with caution.

She said: ‘While these data are the most compelling to date on the potential benefit of ejaculation on prostate cancer development, they are observational data and should be interpreted somewhat cautiously.

‘At the same time, given the lack of modifiable risk factors for prostate cancer, the results of this study are particularly encouraging.’

More than 1.1 million cases of prostate cancer were recorded in 2012, according to the World Cancer Research Fund International. Pictured are prostate cancer cells under a microscope

More than 1.1 million cases of prostate cancer were recorded in 2012, according to the World Cancer Research Fund International. Pictured are prostate cancer cells under a microscope

She added more research should be carried out into the specific changes in the prostate caused by ejaculation, to understand how it reduces the risk of prostate cancer.

The research was presented at the American Urological Society annual meeting in New Orleans in May.

More than 1.1 million cases of prostate cancer were recorded in 2012, accounting for around eight per cent of all new cancer cases and 15 per cent in men, according to figures from the World Cancer Research Fund International.

The causes of prostate cancer are largely unknown, but the chances of developing the disease increase as a man gets older.

 

Patent confirms that aspartame is the excrement of GM bacteria .


In 1999, The Independent published an article entitled “World’s top sweetener is made with GM bacteria,” which revealed that Monsanto was knowingly adding aspartame to soft drinks in the United States – and that aspartame is made from GM bacteria. This report, which remains one of the earliest disclosures on aspartame in a mainstream newspaper, received little attention after its publication – possibly because its implications were underestimated at the time – and it has long been forgotten.

Aspartame

Since 1999, the world has become a little more attentive to Monsanto and aspartame, but ignorance still abounds about the latter’s genesis. While more and more people are starting to awaken to aspartame’s destructive effects on our health, do they know how it is actually made? Fortunately, a 1981 patent for aspartame production, once confined to the drawers of patent offices, is now available online for everyone to see – and it confirms everything that Monsanto was happy to tell us in 1999 before their meteoric growth necessitated greater prudence.

The production process

The patent, which is entitled Process for producing aspartame and is credited to Bahl, Rose, and White, summarizes the process as follows:

“The artificial sweetener aspartame, a dipeptide with the formula Asp-Phe-me, is produced using a cloned micrcorganism [sic]. A DNA which codes for a large stable peptide comprised of the repeating amino acid sequence (Asp-Phe)n is inserted into a cloning vehicle which in turn is introduced into a suitable host microorganism. The host microorganism is cultured and the large peptide containing the repeating Asp-Phe sequence is harvested therefrom. The free carboxyl group of the large peptide is benzylated and then hydrolysed to benzyl Asp-Phe dipeptides. This dipeptide is methylated and then debenzylated to form aspartame.”

This scientific jargon obfuscates (perhaps deliberately) a truly disturbing process:

1.) ‘Cloned microorganisms’ (which the patent later reveals to be genetically modified E. coli) are cultivated in tanks whose environments are tailored to help them thrive.

2.) The well-fed E. coli cultures defecate the proteins that contain the aspartic acid-phenylalanine amino acid segment needed to make aspartame.

3.) The proteins containing the Asp-Phe segments are ‘harvested’ (i.e. lab assistants collect the bacteria’s feces).

4.) The feces are then treated. This includes a process of methylation (adding an excess of the toxic alcohol, methanol, to the protected dipeptide).

While common sense dictates that this abomination doesn’t belong anywhere near our bodies, the patent’s authors made no secret about their belief that aspartame constitutes a safe and nutritious sweetener:

“Aspartame is not only sweeter than sucrose, but is preferable as a food to sucrose. While sucrose can provide the body with little more than energy, aspartame is composed of amino acids, the building blocks of body proteins, and like other proteins is broken down by the digestive enzymes in the stomach to its constituent amino acids thus providing nutritive value. […] For these reasons, aspartame holds significant promise in replacing sugar as a sweetener.”

So there we have it: An official document that not only reveals the shocking truth behind aspartame production, but also freely admits that it was intended for mass consumption as a sucrose substitute. Therefore, the next time someone claims that your reservations about this sweetener are unfounded, direct them to this patent – the truth behind aspartame is now in plain view.

Learn more: http://www.naturalnews.com/041766_aspartame_GM_bacteria_patent.html#ixzz3w6yuHXBJ

15 Year Old Invents Device That Generates Electricity While You Walk


15-year-old Angelo Casimiro from the Philippines recently made international news with a new invention that generates electricity in a very new and interesting way.

The invention is a shoe insole that harnesses electricity every time that the person wearing the shoe takes a step. Angelo constructed his device using piezoelectric materials, which actually generate an alternating current voltage every time they are squeezed.

According to a blog post made by the teenager, “Piezoelectricity was present ever since mid-18th century. Piezoelectricity is the electric charge that accumulates in certain solid materials (such as crystals, certain ceramics in response to applied mechanical stress.”

Young Angelo has been working hard developing this idea for the past 4 years, since he was 11 years old.  Now that he believes he has perfected his invention, he is prepared to share it with the world.  He started by entering the project into this year’s Google’s Science Fair, where he has become a regional finalist.

teenager