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MIT Scientist Shows What Can Happen To Children Who Receive Aluminum Containing Vaccines

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A claim often heard from the “pro-vaccination” community when it comes to linking vaccines to autism is that there is no evidence to substantiate those claims. This view is absolutely absurd and dangerous given the fact that a tremendous amount of scientific evidence exists and is available in the public domain that suggests some vaccines could possibly play a role in the development of autism. To say that there is no probability of some vaccinations contributing to the development of autism contradicts the science.

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When it comes to Monsanto’s glyphosate and other commonly used pesticides (as well as other environmental toxins), the science linking them to possible causes of autism (among many other diseases like Alzheimer’s and cancer) seems to be irrefutable and abundant. You can read more about that here:

Scientists Link Autism To These Toxic Chemicals During Fetal Development

Another Groundbreaking Study Emerges Linking Agricultural Pesticides To Autism

Furthermore, we’ve had statements made from scientists who’ve had long careers with vaccine manufactures, pharmaceutical companies and  health organizations like the CDC. We also have documents that indicate scientific fraud and manipulation of data when it comes to the adverse affects of vaccinations.(1)  Many examples of “funny business” within the food industry are also making their way into the public domain  when it comes to the role of GMO’s and pesticides regarding their link with various diseases. One example (out of many) is the fact that after a study was published showing that two Monsanto products, a genetically modified (GM) maize and Roundup herbicide were linked to cancer, kidney and liver damage, the journal that published the study appointed a former Monsanto scientist to decide which papers on GM foods and crops should be published. The study was then retracted, but has been republished in another journal since. (2) You can read more about (and view) this study HERE.

One thing we now know for sure is that the development of autism goes far beyond genetics.

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The research suggesting that vaccines and glyphosate could possibly play a role in autism comes from various peer-reviewed scientific journals as well as independent research conducted by renowned scientists from all over the world. One of those scientists is Dr. Stephanie Seneff. This article will  focus mostly on her views regarding the connection between aluminum containing vaccines and autism. Information regarding autism and pesticides are linked in two articles above after the first paragraph.

Dr Seneff is a Senior Research Scientist at the MIT Computer Science and Artificial Intelligence Laboratory. In recent years her research has focused specifically on biology, nutrition and health. Within the past three years alone she has written over a dozen papers in multiple medical and health related journals touching upon many modern day diseases such as Alzheimer’s disease and autism (among others). (3)

Vaccines and Autism

In North America alone, millions of doses of vaccines are administered to children every year. Various chemicals are added to the vaccines as preservatives, and theses chemical additives have been responsible for stirring up quite the controversy, especially within the past couple of years. One common substance found in vaccines is aluminum.

A paper published by Dr. Seneff in 2012 argues that severe adverse reactions to the chemicals (like aluminum) within vaccines can be associated with life threatening conditions that are associated with the heart and brain. The paper goes on to argue that there is a relationship between autism and acute adverse reactions to vaccinations.  Dr Seneff is not claiming that vaccines cause autism, she is simply claiming that children could be vulnerable to an acute reaction to an aluminum adjuvanted vaccine, which could cause neuronal damage. (4)

The study also outlines how autism is associated with elevated levels of nitrate in the blood stream, and that aluminum likely plays a role in in the excess nitrate production. Furthermore, the study shows how abnormally high levels of aluminum were recently found in hair analyses of over half of 34 autistic children that were analyzed. Another important factor mentioned in her research is that autism is associated with abnormal immune function, and this (she argues) is enhanced by aluminum adjuvants in vaccines. (4)

In summary, the paper argues that autism develops as a result of a deficiency in the supply of cholesterol sulfate to stabilize the colloidal suspension system of the blood. Cholesterol sulfate supply is maintained by nitrate levels  “acting in the epidermis, the endothelium, and the suspended blood cells, and that it requires the substrates cholesterol and sulfur, as well as sunlight, to provide the necessary activation energy for the reaction.” (4)  Vaccines come into the picture because:

“Aluminum-containing vaccines are problematic, not only because aluminum causes eNOS to switch from sulfate to nitric oxide production, but also because aluminum can induce necrosis of tissues at the vaccination site, emulating  the process of tissue damage to the placenta in preeclampsia. In both cases, the release of
mitochondrial DNA into the blood stream may trigger an acute autoimmune reaction.” (4)

The study concluded that:

“We have proposed in this paper a novel hypothesis for the underlying pathology that links autism, and extreme adverse reactions to vaccines. We would also recommend the elimination of aluminum as an adjuvant in vaccines.” (4)

“Aluminum is an experimentally demonstrated neurotoxin and the most commonly used vaccine adjuvant. Despite almost 90 years of widespread use of aluminum adjuvants, medical science’s medical understanding of their mechanisms of action is still remarkably poor. There is also a concerning scarcity of data on toxicology and pharmacokinetics of these compounds. In spite of this, the notion that aluminum in vaccines is safe appears to be widely accepted.” (5) – Dr. Chris Shaw, with the UBC Departments of Ophthalmology and Visual Sciences and Experimental Medicine and the Graduate Program in Neuroscience

I’d also like to mention that experimental research clearly shows that aluminum in adjuvant form creates a risk for autoimmunity, long-term brain inflammation and subsequent neurological complications and may as a result have profound and widespread adverse health complications.(5)

Professor Christopher Shaw and Dr. Lucija Tomljenovic of UBC (in a recent study) also show that the more children receive vaccines with aluminum adjuvants, the greater their chance is of developing autism, autoimmune diseases and neurological problems later in life.  A demonstrated neurotoxin, Aluminum is the only approved adjuvant in the US.   Its use presents the risk of brain inflammation, autoimmunity and other adverse health consequences.(6)

Just as a side note, it is known that aluminum accumulates in the brain and that this accumulation is associated with Alzheimer’s and Parkinson’s diseases and with Gulf War Syndrome. (7)(8)

“Experimental research clearly shows that aluminum adjuvants have a potential to induce serious immunological disorders in humans. In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation and associated neurological complications and may thus have profound and widespread adverse health consequences.” (source)

A study published in the Journal Pediatrics found that:

“Aluminum is now being implicated as interfering with a variety of cellular and metabolic processes in the nervous system and in other tissues.” (source)

A role for the Pineal Gland In Neurological Damage Following Aluminum Adjuvented Vaccination

The paper discussed above by Dr. Seneff is from 2012. In more recent news regarding Dr. Seneff, she recently presented more scientific research at the Third International Symposium on Vaccines in March 2014. It was part of the 9th International Congress on Autoimmunity. She was invited by the Children’s Medical Safety Research Institute (CMSRI) to discuss the adverse health effects of aluminum adjuvants and aluminum-adjuvented vaccines.

As noted above, Dr. Seneff commonly makes the case that neurological brain diseases are a result of an insufficient supply of sulfate to the brain. She argues that systematic sulfate deficiency “may be the most important factor in many of the health issues facing us today.”

“One of the consequences of insufficient sulfate in the brain is that it impairs the brain’s ability to eliminate heavy metals and other toxins. To make matters worse, those same toxic metals also interfere with sulfate synthesis. The net result can be an accumulation of cellular debris.” – (source) Claire I. Viadro, MPH, PhD

Some interesting studies have been done when it comes to Heparin Sulfate, which also plays a key role in fetal brain development, protecting against damaging free radicals. When it comes to autism and sulfate deficiency, intriguing evidence of what happens when heparan sulfate is deficient comes from both human and mouse studies of autism. In one study, “mice engineered to have impaired heparan sulfate synthesis in the brain displayed all the classic features of autism, including sociocommunicative deficits and stereotypies.” (9) (animal testing is cruel, unnecessary and not needed anymore. There are alternative methods that now exist researchers can use to do their testing.)

Another study published in the Journal Behavioural Brain Research found that this type of deficiency exists in the subventricular zone of the lateral ventricles of four autistic people. The authors concluded that this “may be a biomarker for autism, and potentially involved in the etiology of the disorder.” (10)

What Dr. Seneff is suggesting is that melatonin is a key factor in the delivery of sulfate to the brain. That sunlight exposure helps the pineal gland build up supplies of sulfate by the day, storing it in heparan sulfate molecules. When the evening comes around, the pineal gland produces melatonin, and transports it as melatonin sulfate to several parts of the brain. The significance here is that there is an association of autism with heparan sulfate depletion in the lateral and third ventricles, and the tip of the third ventricle is located within the pineal gland. (source) When everything is working how it’s supposed to be working, the pineal gland delivers sulfate to the third ventricle, among other parts of the brain. But when the brain is loaded with toxic chemicals, like aluminum, it hinders that process.

 “In addition, melatonin not only transports sulfate but also is an outstanding antioxidant and binds toxic metals to help dispose of them. It may come as no surprise, then, that melatonin impairment has been implicated in autism.” – (source) Claire I. Viadro, MPH, PhD

As far as aluminum goes, it’s a well known fact that it plays a role in various neurological diseases, and that it may disrupt the pineal glands ability to produce sulfate, which means the brain cannot cleanse itself of heavy metals and they just continue to accumulate.

“The pineal gland is particularly susceptible to aluminum and other heavy metals because it is not protected by the blood-brain barrier and has a very high blood perfusion rate.” (source) Claire I. Viadro, MPH, PhD

The pineal gland’s vulnerability to aluminum is illustrated in a 1996 paper showing that the concentrations of aluminum in the pineal gland were “consistently observed” and “markedly higher” than in other brain tissues examined (pituitary, cortex, and cerebellum) (11)

“Scientists are taking note of the fact that we live in an “age of aluminum,” with aluminum exposure occurring through vaccines as well as multiple other channels. Moreover, although many experts would have us believe that the question of thimerosal and vaccine safety went away after federal agencies issued lukewarm recommendations to reduce its use as a vaccine preservative in the early 2000s, Dr. Seneff noted that thimerosal is still very much relevant.” (source) Claire I. Viadro, MPH, PhD

In summary, Dr. Seneff is pointing to the fact that many neurological diseases of the brain have a common origin, which includes an insufficient supply of sulfate to the brain. She is concluding that enhanced toxic metal exposure (aluminum) impairs the brains ability to detox itself and eliminate them. As a result, these toxic metals interfere with sulfate synthesis, create a heparan sulfate deficency which in turn leads to autism (as mentioned and pointed out with the studies cited above.) (12)

I’d also like to mention that autism is comprised of a very large spectrum. Some of the ailments associated with diagnosis might not be ailments at all, but gifts that are in no way associated with vaccines. On the other hand, I do believe in some cases, characteristics that are seen in some autistic children are the cause of various toxins from pesticides to vaccines, especially children who have a genetic make up that makes them more sensitive to these chemicals. In some cases (I believe) it’s a result of these various toxins, and again, in other cases I believe it is a gift, and possibly an evolutionary step.

 Sources:

(1) http://nsnbc.me/wp-content/uploads/2013/05/BSEM-2011.pdf

(2) http://earthopensource.org/index.php/news/148-former-monsanto-employee-put-in-charge-of-gmo-papers-at-journal

(3) http://people.csail.mit.edu/seneff/

(4) http://people.csail.mit.edu/seneff/Entropy/entropy-14-02265.pdf

(5) http://www.ncbi.nlm.nih.gov/pubmed/21568886

(6) http://www.ncbi.nlm.nih.gov/pubmed/23609067

(7) http://www.ncbi.nlm.nih.gov/pubmed/1637136

(8) http://www.ncbi.nlm.nih.gov/pubmed/14743440

(9) http://www.pnas.org/content/109/13/5052.long

(10) http://www.ncbi.nlm.nih.gov/pubmed/23318464

 (11) http://www.99thagent.org/freddyspyder/files/108Piezoelectricity.pdf

(12) http://people.csail.mit.edu/seneff/SeneffNice2014.pdf

http://pediatrics.aappublications.org/content/97/3/413.abstract

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Legal Challenge Against Forced Vaccination Filed in New York City

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On April 15, 2019, a legal challenge was filed in the New York State Trial Court by Robert Krakow, Robert F. Kennedy, Jr. and Patricia Finn against the New York City Department of Health and Human Hygiene for their forced Measles-Mumps-Rubella vaccination. The legal team asked for a temporary restraining order against the mandate that the Judge will likely review and provide an ex parte decision. Children’s Health Defense is supporting these efforts.

Last week, Children’s Health Defense reported that the NYC Commissioner of Health declared a public health emergency, ordering all people who live, work or reside in four Brooklyn zip codes to be vaccinated with the Measles-Mumps-Rubella vaccine. Non-compliance with the order is a misdemeanor subject to criminal and civil fines, including imprisonment. Only those with documented immunity, medical contraindications or infants under six months are exempt from the vaccine mandate.

READ THE PETITION
READ THE MEMORANDUM OF LAW
READ THE AFFIRMATION

Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. CHD is planning many strategies, including legal, in an effort to defend the health of our children and obtain justice for those already injured. Your support is essential to CHD’s successful mission.

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Magnesium Puts Psychiatric Drugs to Shame for Depression

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In Brief

  • The Facts:

    This article was written by Sayer Ji, Founder of Greenmedinfo.com where this article first appeared. Posted here with permission.

  • Reflect On:

    Is the priority of our federal health regulatory agencies and pharmaceutical companies human health, or profit? If there are more effective ways to treat several illnesses, why do they never mention them?

Depression is one of the most widely diagnosed conditions of our time, with over 3 million cases in the U.S. every year, and 350 million believed affected worldwide.1 Conventional medicine considers antidepressant drugs first-line treatments, including the newly approved injected postpartum drug costing $34,000 a treatment, to the tune of a 16 billion dollars in global sales by 2023. Despite their widespread use, these drugs are fraught with a battery of serious side effects, including suicidal ideation and completion — the last two things you would hope to see in a condition that already has suicidality as a co-morbidity. For this reason alone, natural, safe, and effective alternatives are needed more than ever before.

While research into natural alternatives for depression is growing daily — GreenMedInfo.com’s Depression database contains 647 studies on over 100 natural substances that have been studied to prevent or treat depression — it is rare to find quality human clinical research on the topic published in well-respected journals. That’s why a powerful study published in PLOS One titled, “Role of magnesium supplementation in the treatment of depression: A randomized clinical trial,” is so promising. Not only is magnesium safe, affordable, and easily accessible, but according to this recent study, effective in treating mild-to moderate symptoms of depression.

While previous studies have looked at the association between magnesium and depression,2-7 this is the first placebo-controlled clinical study to evaluate whether the use of over-the-counter magnesium chloride (248 mg elemental magnesium a day for 6 weeks) improves symptoms of depression.

The study design was a follows:

“ An open-label, blocked, randomized, cross-over trial was carried out in outpatient primary care clinics on 126 adults (mean age 52; 38% male) diagnosed with and currently experiencing mild-to-moderate symptoms with Patient Health Questionnaire-9 (PHQ-9) scores of 5–19. The intervention was 6 weeks of active treatment (248 mg of elemental magnesium per day) compared to 6 weeks of control (no treatment). Assessments of depression symptoms were completed at bi-weekly phone calls. The primary outcome was the net difference in the change in depression symptoms from baseline to the end of each treatment period. Secondary outcomes included changes in anxiety symptoms as well as adherence to the supplement regimen, appearance of adverse effects, and intention to use magnesium supplements in the future. Between June 2015 and May 2016, 112 participants provided analyzable data.”

The study results were as follows:

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“Consumption of magnesium chloride for 6 weeks resulted in a clinically significant net improvement in PHQ-9 scores of -6.0 points (CI -7.9, -4.2; P<0.001) and net improvement in Generalized Anxiety Disorders-7 scores of -4.5 points (CI -6.6, -2.4; P<0.001). Average adherence was 83% by pill count. The supplements were well tolerated and 61% of participants reported they would use magnesium in the future. Similar effects were observed regardless of age, gender, baseline severity of depression, baseline magnesium level, or use of antidepressant treatments. Effects were observed within two weeks. Magnesium is effective for mild-to-moderate depression in adults. It works quickly and is well tolerated without the need for close monitoring for toxicity.”

 For perspective, conventional antidepressant drugs are considering to generate an “adequate or complete treatment response” with a PHQ-9 score “decrease of 5 points or more from baseline.” At this level of efficacy, their recommended action is: “Do not change treatment; conduct periodic follow-up.” The magnesium’s score of -6.0 therefore represents the height of success within conventional expectations for a complete response, which is sometimes termed “remission.” In contradistinction, conventional antidepressant drugs result in nearly half of patients discontinuing treatment during the first month, usually due to their powerful and sometimes debilitating side effects.8

To summarize the main study outcomes:

  • There was a clinically significant improvement in both Depression and Anxiety scores.
  • 61% of patients reported they would use magnesium in the future.
  • Similar effects occurred across age, gender, severity of depression, baseline magnesium levels, or use of antidepressant treatments.
  • Effects were observed within two weeks.

 The study authors concluded:

“Magnesium is effective for mild-to-moderate depression in adults. It works quickly and is well tolerated without the need for close monitoring for toxicity.”

Beyond Depression: Magnesium’s Many Health Benefits & Where To Source It

Magnesium is a central player in your body’s energy production, as its found within 300 enzymes in the human body, including within the biologically active form of ATP known as MG-ATP. In fact, there have been over 3,751 magnesium binding sites identified within human proteins, indicating that it’s central nutritional importance has been greatly underappreciated.

Research relevant to magnesium has been accumulating for the past 40 years at a steady rate of approximately 2,000 new studies a year. Our database project has indexed well over 100 health benefits of magnesium thus far.  For the sake of brevity, we will address seven key therapeutic applications for magnesium as follows:

  • Fibromyalgia: Not only is magnesium deficiency common in those diagnosed with fibromyalgia, 9,10 but relatively low doses of magnesium (50 mg), combined with malic acid in the form of magnesium malate, has been clinically demonstrated to improve pain and tenderness in those to which it was administered.11
  • Atrial Fibrillation: A number of studies now exist showing that magnesium supplementation reduce atrial fibrillation, either by itself, or in combination with conventional drug agents.12
  • Diabetes, Type 2: Magnesium deficiency is common in type 2 diabetics, at an incidence of 13.5 to 47.7% according to a 2007 study. 13 Research has also shown that type 2 diabetics with peripheral neuropathy and coronary artery disease have lower intracellular magnesium levels. 14 Oral magnesium supplementation has been shown to reduce plasma fasting glucose and raising HDL cholesterol in patients with type 2 diabetes.15 It has also been shown to improve insulin sensitivity and metabolic control in type 2 diabetic subjects.16
  • Premenstrual Syndrome: Magnesium deficiency has been observed in women affected by premenstrual syndrome.17 It is no surprise therefore  that it has been found to alleviate premenstrual symptoms of fluid retention, 18 as well as broadly reducing associated symptoms by approximately 34% in women, aged 18-45, given 250 mg tablets for a 3-month observational period.20 When combined with B6, magnesium supplementation has been found to improve anxiety-related premenstrual symptoms.19
  • Cardiovascular Disease and Mortality: Low serum magnesium concentrations predict cardiovascular and all-cause mortality.21 There are a wide range of ways that magnesium may confer its protective effects. It may act like a calcium channel blocker,22it is hypotensive,23 it is antispasmodic (which may protect against coronary artery spasm),24 and anti-thrombotic.25 Also, the heart muscle cells are exceedingly dense in mitochondria (as high as 100 times more per cell than skeletal muscle), the “powerhouses” of the cell,” which require adequate magnesium to produce ATP via the citric acid cycle.
  • Migraine Disorders: Blood magnesium levels have been found to be significantly lower in those who suffer from migraine attacks.26,27 A recent Journal of Neural Transmission article titled, “Why all migraine patients should be treated with magnesium,” pointed out that routine blood tests do not accurately convey the true body magnesium stores since less than 2% is in the measurable, extracellular space, “67% is in the bone and 31% is located intracellularly.”28The authors argued that since “routine blood tests are not indicative of magnesium status, empiric treatment with at least oral magnesium is warranted in all migraine sufferers.” Indeed, oral magnesium supplementation has been found to reduce the number of headache days in children experiencing frequent migranous headaches,29and when combined with l-carnitine, is effective at reducing migraine frequency in adults, as well.30
  • Aging: While natural aging is a healthy process, accelerated aging has been noted to be a feature of magnesium deficiency,31especially evident in the context of long space-flight missions where low magnesium levels are associated with cardiovascular aging over 10 times faster than occurs on earth.32 Magnesium supplementation has been shown to reverse age-related neuroendocrine and sleep EEG changes in humans.33 One of the possible mechanisms behind magnesium deficiency associated aging is that magnesium is needed to stabilize DNA and promotes DNA replication. It is also involved in healing up of the ends of the chromosomes after they are divided in mitosis.34

 It is quite amazing to consider the afformentioned side benefits of magnesium consumption or supplementation within the context of the well-known side effects of pharmaceutical approaches to symptom

management of disease. On average, conventional drugs have 75 side effects associated with their use, including lethal ones (albeit sometimes rare). When considering magnesium’s many side benefits

and extremely low toxicity, clearly this fundamental mineral intervention (and dietary requirement) puts pharmaceutical approaches to depression to shame.

Best Sources of Magnesium In The Diet

The best source of magnesium is from food, and one way to identify magnesium-containing foods are those which are green, i.e. chlorophyll rich. Chlorophyll, which enable plants to capture solar energy and convert it into metabolic energy, has a magnesium atom at its center. Without magnesium, in fact, plants could not utilize the sun’s light energy.

Magnesium, however, in its elemental form is colorless, and many foods that are not green contain it as well. The point is that when found complexed with food cofactors, it is absorbed and utilized more efficiently than in its elemental form, say, extracted from limestone in the form of magnesium oxide.

 The following foods contain exceptionally high amounts of magnesium. The portions described are 100 grams, or a little over three ounces.

  • Rice bran, crude (781 mg)
  • Seaweed, agar, dried (770 mg)
  • Chives, freeze-dried (640 mg)
  • Spice, coriander leaf, dried (694 mg)
  • Seeds, pumpkin, dried (535 mg)
  • Cocoa, dry powder, unsweetened (499 mg)
  • Spices, basil, dried (422 mg)
  • Seeds, flaxseed (392 mg)
  • Spices, cumin seed (366 mg)
  • Nuts, brazilnuts, dried (376 mg)
  • Parsley, freeze-dried (372 mg)
  • Seeds, sesame meal (346 mg)
  • Nut, almond butter (303 mg)
  • Nuts, cashew nuts, roasted (273 mg)
  • Soy flour, defatted (290 mg)
  • Whey, sweet, dried (176 mg)
  • Bananas, dehydrated (108 mg)
  • Millet, puffed (106 mg)
  • Shallots, freeze-dried (104 mg)
  • Leeks, freeze-dried (156 mg)
  • Fish, salmon, raw (95 mg)
  • Onions, dehydrated flakes (92 mg)
  • Kale, scotch, raw (88 mg)

 Fortunately, for those who need higher doses, or are not inclined to consume magnesium rich foods, there are supplemental forms commonly available on the market. Keep in mind, for those who wish to take advantage of the side benefit of magnesium therapy, namely, its stool softening and laxative properties, magnesium citrate or oxide will provide this additional feature.

For those looking to maximize absorption and bioavailability magnesium glycinate is ideal, as glycine is the smallest amino acid commonly found chelated to magnesium, and therefore highly absorbable.

For more information on natural solutions to resolving depression, download our free e-book on the topic “21st Century Solutions to Depression.” 

References:

1) World Health Organization. Depression fact sheet no. 369 2012 [cited 2016 December 20]. Available from: http://www.who.int/mediacentre/factsheets/fs369/en/.

2) Jacka FN, Overland S, Stewart R, Tell GS, Bjelland I, Mykletun A. Association between magnesium intake and depression and anxiety in community-dwelling adults: the Hordaland Health Study. Aust N Z J Psychiatry. 2009;43(1):45–52. Pmid:19085527.

3) Huang JH, Lu YF, Cheng FC, Lee JN, Tsai LC. Correlation of magnesium intake with metabolic parameters, depression and physical activity in elderly type 2 diabetes patients: a cross-sectional study. Nutrition J. 2012;11(1):41. pmid:22695027; PubMed Central PMCID: PMC3439347.

4) Tarleton EK, Littenberg B. Magnesium intake and depression in adults. J Am Board Fam Med. 2015;28(2):249–56. Pmid:25748766

5) Yary T, Lehto SM, Tolmunen T, Tuomainen T-P, Kauhanen J, Voutilainen S, et al. Dietary magnesium intake and the incidence of depression: a 20-year follow-up study. J Affect Disord. 2016;193:94–8. Pmid:26771950

6) Eby GA, Eby KL. Rapid recovery from major depression using magnesium treatment. Med Hypotheses. 2006;67(2):362–70. pmid:16542786

7) N Engl J Med. 2000 Dec 28;343(26):1942-50. Managing depression in medical outpatients.

8)  Damiano Piovesan, Giuseppe Profiti, Pier Luigi Martelli, Rita Casadio. 3,751 magnesium binding sites have been detected on human proteins. BMC Bioinformatics. 2012 ;13 Suppl 14:S10. Epub 2012 Sep 7. PMID: 23095498

9) G Moorkens, B Manuel y Keenoy, J Vertommen, S Meludu, M Noe, I De Leeuw. Magnesium deficit in a sample of the Belgian population presenting with chronic fatigue. Magnes Res. 1997 Dec;10(4):329-37. PMID: 9513929

10)  J Eisinger, A Plantamura, P A Marie, T Ayavou. Selenium and magnesium status in fibromyalgia. Magnes Res. 1994 Dec;7(3-4):285-8. PMID: 7786692

11)  I J Russell, J E Michalek, J D Flechas, G E Abraham. Treatment of fibromyalgia syndrome with Super Malic: a randomized, double blind, placebo controlled, crossover pilot study. J Rheumatol. 1995 May;22(5):953-8. PMID: 8587088

12) GreenMedInfo.com, Atrial Fibrillation and Magnesium (5 studies)

13)  Phuong-Chi T Pham, Phuong-Mai T Pham, Son V Pham, Jeffrey M Miller, Phuong-Thu T Pham . Hypomagnesemia in patients with type 2 diabetes. Clin J Am Soc Nephrol. 2007 Mar;2(2):366-73. Epub 2007 Jan 3. PMID: 17699436

14)  M de Lordes Lima, T Cruz, J C Pousada, L E Rodrigues, K Barbosa, V Canguçu. The effect of magnesium supplementation in increasing doses on the control of type 2 diabetes. Diabetes Care. 1998 May;21(5):682-6. PMID: 9589224

15) Y Song, K He, E B Levitan, J E Manson, S Liu. Effects of oral magnesium supplementation on glycaemic control in Type 2 diabetes: a meta-analysis of randomized double-blind controlled trials. Cardiovasc Toxicol. 2008;8(3):115-25. Epub 2008 Jul 8. PMID: 16978367

16)  Martha Rodríguez-Morán, Fernando Guerrero-Romero. Oral magnesium supplementation improves insulin sensitivity and metabolic control in type 2 diabetic subjects: a randomized double-blind controlled trial. Diabetes Care. 2003 Apr;26(4):1147-52. PMID: 12663588

17)  F Facchinetti, P Borella, G Sances, L Fioroni, R E Nappi, A R Genazzani. Oral magnesium successfully relieves premenstrual mood changes. Obstet Gynecol. 1991 Aug;78(2):177-81. PMID: 2067759

18)  A F Walker, M C De Souza, M F Vickers, S Abeyasekera, M L Collins, L A Trinca. Magnesium supplementation alleviates premenstrual symptoms of fluid retention. J Womens Health. 1998 Nov;7(9):1157-65. PMID: 9861593

19)  S Quaranta, M A Buscaglia, M G Meroni, E Colombo, S Cella. Pilot study of the efficacy and safety of a modified-release magnesium 250 mg tablet (Sincromag) for the treatment of premenstrual syndrome. Am J Gastroenterol. 2008 Dec;103(12):2972-6. PMID: 17177579

20) M C De Souza, A F Walker, P A Robinson, K Bolland. A synergistic effect of a daily supplement for 1 month of 200 mg magnesium plus 50 mg vitamin B6 for the relief of anxiety-related premenstrual symptoms: a randomized, double-blind, crossover study. J Womens Health Gend Based Med. 2000 Mar;9(2):131-9. PMID: 10746516

21) Thorsten Reffelmann, Till Ittermann, Marcus Dörr, Henry Völzke, Markus Reinthaler, Astrid Petersmann, Stephan B Felix. Low serum magnesium concentrations predict cardiovascular and all-cause mortality. Atherosclerosis. 2011 Jun 12. Epub 2011 Jun 12. PMID: 21703623

22) Andrea Rosanoff, Mildred S Seelig. Comparison of mechanism and functional effects of magnesium and statin pharmaceuticals. J Am Coll Nutr. 2004 Oct;23(5):501S-505S. PMID: 15466951

23)  GreenMedInfo.com, Magnesium’s Hypotensive Properties.

24) GreenMedInfo.com, Magnesium’s Antispasmodic Properties.

25) Joen R Sheu, George Hsiao, Ming Y Shen, Yen M Lee, Mao H Yen . Antithrombotic effects of magnesium sulfate in in vivo experiments. Int J Hematol. 2003 May;77(4):414-9. PMID: 12774935

26) Afshin Samaie, Nabiollah Asghari, Raheb Ghorbani, Jafar Arda. Blood Magnesium levels in migraineurs within and between the headache attacks: a case control study. Pan Afr Med J. 2012 ;11:46. Epub 2012 Mar 15. PMID: 22593782

27) Mahnaz Talebi, Dariush Savadi-Oskouei, Mehdi Farhoudi, Solmaz Mohammadzade, Seyyedjamal Ghaemmaghamihezaveh, Akbar Hasani, Amir Hamdi. Relation between serum magnesium level and migraine attacks. Neurosciences (Riyadh). 2011 Oct ;16(4):320-3. PMID: 21983373

28) Alexander Mauskop, Jasmine Varughese. Why all migraine patients should be treated with magnesium. J Neural Transm. 2012 May ;119(5):575-9. Epub 2012 Mar 18. PMID: 22426836

29)  Fong Wang, Stephen K Van Den Eeden, Lynn M Ackerson, Susan E Salk, Robyn H Reince, Ronald J Elin. Oral magnesium oxide prophylaxis of frequent migrainous headache in children: a randomized, double-blind, placebo-controlled trial. Eur J Endocrinol. 2009 Apr;160(4):611-7. Epub 2009 Jan 29. PMID: 12786918

30) Ali Tarighat Esfanjani, Reza Mahdavi, Mehrangiz Ebrahimi Mameghani, Mahnaz Talebi, Zeinab Nikniaz, Abdolrasool Safaiyan. The effects of magnesium, L-carnitine, and concurrent magnesium-L-carnitine supplementation in migraine prophylaxis. Biol Trace Elem Res. 2012 Dec ;150(1-3):42-8. Epub 2012 Aug 17. PMID: 22895810

31) David W Killilea, Jeanette A M Maier. A connection between magnesium deficiency and aging: new insights from cellular studies. Magnes Res. 2008 Jun;21(2):77-82. PMID: 18705534

32) GreenMedInfo.com, What We Learned From The Accelerated Aging of Astronauts

33) Katja Held, I A Antonijevic, H Künzel, M Uhr, T C Wetter, I C Golly, A Steiger, H Murck. Oral Mg(2+) supplementation reverses age-related neuroendocrine and sleep EEG changes in humans. Pharmacopsychiatry. 2002 Jul;35(4):135-43. PMID: 12163983

34) William J Rowe. Correcting magnesium deficiencies may prolong life. Clin Interv Aging. 2012 ;7:51-4. Epub 2012 Feb 16. PMID: 22379366


Sayer Ji is founder of Greenmedinfo.com, a reviewer at the International Journal of Human Nutrition and Functional Medicine, Co-founder and CEO of Systome Biomed, Vice Chairman of the Board of the National Health Federation, Steering Committee Member of the Global Non-GMO Foundation.


For more info from Greenmedinfo, you can join their newsletter by clicking here.


Link to original article. 

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Monsanto Has Been Knowingly Lying About the Safety Of Roundup In Their Ads For Decades

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In Brief

  • The Facts:

    In 1996, Monsanto was sued by the New York Attorney General based on its false and misleading advertising of Roundup products. Monsanto lost and agreed to stop, but to date they have not stopped those practices anywhere other than New York State.

  • Reflect On:

    How can we use the egregious assault on our health and well-being at the hands of corporations like Bayer-Monsanto to catalyze our awakening and our motivation to build the type of world we would most prefer to live in?

In the wake of a second lawsuit against Monsanto (now owned by Bayer) ruled in favor of defendant Edwin Hardeman to the tune of $80 million, it is starting to look like Monsanto has simply gone to the well too often–a well that they themselves have poisoned. Years of denying that Roundup’s active ingredient glyphosate causes cancer, years of fabricating ‘scientific’ studies to back up this claim, and years of advertising Roundup as safe when they knew it was anything but is now coming back to haunt them, and may eventually put their very survival in danger.

Related CE Article:Bayer (Monsanto) Loses Billions As Another Jury Determines Roundup Herbicide Causes Cancer

What is perhaps most poignant in the settlement is the fact that Hardeman received about $5 million for compensatory damages, based on the fact that his exposure to glyphosate was shown to have caused his cancer, but was awarded an additional $75 million for punitive damages, based on the fact that ‘Monsanto was negligent by not using reasonable care to warn about Roundup’s NHL <Non-Hodgkins Lymphoma> risk.’ (source)

This is telling Monsanto that their most egregious crime was not the fact that their product caused someone’s cancer, but that they intentionally withheld known dangers from the public in their labeling and promotion of the product.

How Do We Know Monsanto Has Been Lying?

How can we say for sure that Monsanto knows that it is promoting false ideas about the safety of Roundup to the public? We only need to dig a little into the case files to see the type of evidence that convinced jurors that they are doing so.

In the first case that Monsanto lost to Dewayne Johnson not too long ago (which we wrote about here and here), the prosecutor revealed that in 1996, Monsanto was sued by the New York Attorney General based on its false and misleading advertising of Roundup products. They ended up agreeing to an ‘Assurance of Discontinuance’ with New York State wherein Monsanto would stop making advertisements that made certain unsubstantiated claims about the safety of Roundup.

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A discussion of this piece of evidence between Joe Martino and I is captured in the video below, part of a larger discussion about Bayer-Monsanto and the pharmaceutical industry in our bi-weekly news broadcast ‘The Collective Evolution Show’ available on CETV:

Here is the precise way it was presented in the complaint document of Dewayne Johnson’s lawsuit:

Monsanto has known for decades that it falsely advertises the safety of Roundup

42. In 1996, the New York Attorney General (“NYAG”) filed a lawsuit against Monsanto based on its false and misleading advertising of Roundup products. Specifically, the lawsuit challenged Monsanto’s general representations that its spray-on glyphosate-based herbicides, including Roundup, were “safer than table salt” and “practically non-toxic” to mammals, birds, and fish. Among the representations of the NYAG found deceptive and misleading about the human and environmental safety of Roundup are the following:

A) Remember that environmentally friendly Roundup herbicide is biodegradable. It won’t build up in the soil so you can use Roundup with confidence along customers’ driveways, sidewalks, and fences…

B) And remember that Roundup is biodegradable and won’t build up in the soil. That will give you the environmental confidence you need to use Roundup everywhere you’ve got a weed, brush, edging or trimming problem.

C) Roundup biodegrades into naturally occurring elements.

D) Remember that versatile Roundup herbicide stays where you put it. That means there’s no washing or leaching to harm customers’ shrubs or other desirable vegetation.

E) This non-residual herbicide will not wash or leach in the soil. It…stays where you apply it.

F) You can apply Accord with “confidence because it will stay where you put it,” it bonds tightly to soil particles, preventing leaching. Then, soon after application, soil microorganisms biodegrade Accord into natural products.

G) Glyphosate is less toxic to rats than table salt following accuse oral ingestion.

H) Glyphosate’s safety margin is much greater than required. It has over a 1,000-fold safety margin in food and over a 700-fold safety margin for workers who manufacture it or use it.

I) You can feel good about using herbicides by Monsanto. They carry a toxicity category rating of ‘practically non-toxic’ as it pertains to mammals, birds, and fish.

J) “Roundup can be used where kids and pets will play and break down into natural material.” This ad depicts a person with his head in the ground and a pet dog standing in an area which has been treated with Roundup.

43. On November 19, 1996, Monsanto entered into an Assurance of Discontinuance with NYAG, in which Monsanto agreed, among other things, “to cease and desist from publishing or broadcasting any advertisements [in New York] that represent, directly or by implication” that:

A) its glyphosate-containing pesticide products or any component thereof are safe, non-toxic, harmless, or free from risk.

B) Its glyphosate-containing pesticide products or any component thereof manufactured, formulated, distributed or sold by Monsanto are biodegradable.

C) its glyphosate-containing pesticide products or any component thereof stay where they are applied under all circumstances and will not move through the environment by any means.

D) its glyphosate-containing pesticide products or any component thereof are “good” for the environment or are “known for their environmental characteristics.”

E) glyphosate-containing pesticide products or any component thereof are safer or less toxic than common consumer products other than herbicides.

F) its glyphosate-containing pesticide products or any component thereof night be classified as “practically non-toxic.”

44. Monsanto did not alter its advertising in the same manner in any state other than New York, and on information and belief still has not done so today.

One of the reasons this is so compelling is that it shows Monsanto being forced to acknowledge that it was using deceptive practices, but that it made absolutely no effort to stop this deceptive practice in any other state than the one they were forced to. It is evidence like this that is starting to make people realize that we can no longer give corporations the benefit of the doubt when it comes to their claims that their products are safe for human beings and for the environment.

The Takeaway

As information of this kind comes more into the public eye, and as we become more aware that corporations are willfully putting public health at risk simply for the sake of profit, our collective wheels will start turning with thoughts about the type of world we want to live in, imbued with a sense of urgency around creating a system within which human safety and health are much more highly valued.

Help Support Collective Evolution

The demand for Collective Evolution's content is bigger than ever, except ad agencies and social media keep cutting our revenues. This is making it hard for us to continue.

In order to stay truly independent, we need your help. We are not going to put up paywalls on this website, as we want to get our info out far and wide. For as little as $3 a month, you can help keep CE alive!

SUPPORT CE HERE!

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