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Scientific Evidence Suggests The Vaccine-Autism Link Can No Longer Be Ignored

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Vaccine-childConcerns regarding vaccinations continue to increase exponentially in light of all of the information and documentation that has surfaced over the past few years. As a result, corporate media has responded to alternative media, stating that the increase of persons who are choosing to opt out of vaccines and the recommended vaccine schedule is a result of ‘fear mongering.’ This may not be too surprising as the corporate media is owned by the major vaccine manufacturers, and the major vaccine manufacturers are owned by corporate media(1)(2)(3)(4). Given this fact, it’s easy to fathom the possibility that these institutions are desperately trying to protect the reputation of their product.

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For example, if we take a look at GlaxoSmithKline and Pfizer, they are owned by the same financial institutions and groups that own Time Warner (CNN, HBO etc.) and General Electric (NBC, Comcast, Universal Pictures etc.).(1)(2)(3)(4) This is seen throughout all of the major vaccine manufacturers and all of the 6 corporations that control our mainstream media. Keep in mind that these are the major funders of all ‘medical research’ that’s used to administer drugs and vaccinations. Despite these connections, medical research and documentation exists to show that vaccines might indeed be a cause for concern.

Vaccines and Autism, Both Sides of The Coin

Here we will simply present information from both sides of the coin because many are not even aware that two sides exist. We’ve presented multiple studies, citing multiple research papers and published research conducted by doctors and Universities from all across the world.  Here is an example of a paper that describes how vaccine manufactures and medical ‘experts’ with drug industry connections have been aware of the multiple dangers associated with vaccinations for over 30 years. We’d also like to present medical research that indicates the many dangers associated with vaccines, and have done this on multiple occasions. We do this because the safety of vaccinations is commonly pushed by the mainstream media, without ever mentioning or citing the abundant medical research that should also be taken into consideration when discussing vaccinations. Please keep in mind that there is evidence on both sides. At the same time, some of the evidence on the side that negates a positive outlook on vaccination has been labelled fraudulent, but then again many haven’t.

The vaccine-autism debate has been going on for years. It has been a tale of shifting beliefs as child vaccination rates remain high. On February 1998, Andrew Wakefield, a British gastroenterologist and his colleagues published a paper that supposedly linked Autism to Vaccines(5). More specifically, he claimed that the MMR vaccine was responsible for intestinal inflammation that led to translocation of usually non-permeable peptides to the bloodstream and, subsequently, to the brain, where they affected development(5). His work was unpublished, and he lost his medical license despite the fact multiple studies seem to support Andrew Wakefield’s work (here is one example, and here is another.) He has been labelled a fraud by the mainstream medical world, some experts claim that his research and methods are weak and based on very little evidence. Dr Wakefield’s research will NOT be used in this article.

At the same time I must mention that multiple studies from around the world have concluded that there is no link between Autism and the MMR Vaccine(5). It can become quite a confusing subject given that we have multiple medical studies contradicting each other. Was Dr. Wakefield exposing something that the medical industry did not want you to know? It is known that vaccine manufacturers suppress harmful data regarding their product, as mentioned and illustrated earlier in the article. Regardless of the MMR vaccine and autism debate, there are still a number of studies that link vaccines to a possible autism connection. Please keep in mind that multiple courts worldwide have ruled in favour of vaccines causing autism, brain damage and other complications (6)(7), that include the MMR vaccine.

Here is a great video narrated by Rob Schneider outlining the vaccine-autsim link. Below that you will find a list of 22 medical studies that show possible connections to vaccines and autism. Please keep in mind that we’ve only presented 22 studies here, there are many more published papers that document the link. Hopefully this inspires you to further your research on the subject. Also keep in mind that Autism is only one of the multiple shown consequences of vaccine administration, as they have been linked to a number of other ailments. 

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 1. A study published in the Journal Annals of Epidemiology has shown that giving the Hepatitis B vaccine to newborn baby boys could triple the risk of developing an autism spectrum disorder compared to boys who were not vaccinated as neonates. The  research was conducted at Stony Brook University Medical Centre, NY.

2. A study published in the Journal of Inorganic Biochemistry  by researchers at the Neural Dynamics Group, Department of Ophthalmology and Visual Sciences at the University of British Columbia determined that Aluminum, a highly neurotoxic metal and the most commonly used vaccine adjuvant may be a significant contributing factor to the rising prevalence of ASD in the Western World.  They showed that the correlation between ASD prevalence and the Aluminum adjuvant exposure appears to be the highest at 3-4 months of age. The studies also show that children from countries with the highest ASD appear to have a much higher exposure to Aluminum from vaccines. The study points out that several prominent milestones of brain development coincide with major vaccination periods for infants. These include the onset of synaptogenesis (birth), maximal growth velocity of the hippocampus and the onset of amygdala maturation. Furthermore, major developmental transition in many bio-behavioural symptoms such as sleep, temperature regulation, respiration and brain wave patterns, all of which are regulated by the neuroendocrine network. Many of these aspects of brain function are known to be impaired in autism, such as sleeping and brain wave patterns.

According to the FDA, vaccines represent a special category of drugs as they are generally given to healthy individuals. Further according to the FDA, “this places significant emphasis on their vaccine safety”. While the FDA does set an upper limit for Aluminum in vaccines at no more that 850/mg/dose, it is important to note that this amount was selected empirically from data showing that Aluminum in such amounts enhanced the antigenicity of the vaccine, rather than from existing safety. Given that the scientific evidence appears to indicate that vaccine safety is not as firmly established as often believed, it would seem ill advised to exclude paediatric vaccinations as a possible cause of adverse long-term neurodevelopment outcomes , including those associated with autism.

3. A study published in the Journal of Toxicology and Environmental Health, Part A: Current Issues by the Department of Economics and Finance at the University of New York shows how researchers suspect one or more environmental triggers are needed to develop autism, regardless of whether individuals have a genetic predisposition or not. They determined that one of those triggers might be the “battery of vaccinations that young children receive.” Researchers found a positive and statistically significant relationship between autism and vaccinations. They determined that the higher the proportion of children receiving recommended vaccinations, the higher the prevalence of autism. A 1 % increase in vaccination was associated with an additional 680 children having autism. The results suggest that vaccines may be linked to autism and encourages more in depth study before continually administering these vaccines.

4. A study published in the Journal of Toxicology by the Department of Neurosurgery at The Methodist Neurological Institute in Houston has shown that ASD is a disorder caused by a problem in brain development. They looked at B-cells and their sensitivity levels to thimerosal, a commonly used additive in many vaccines. They determined that ASD patients have a heightened sensitivity to thimerosal which would restrict cell proliferation that is typically found after vaccination. The research shows that individuals who have this hypersensitivity to thimerosal could make them highly susceptible to toxins like thimerosal, and that individuals with a mild mitochondrial defect may be affected by thimerosal. The fact that ASD patients’ B cells exhibit hypersensitivity to thimerosal tells us something.

5. A study published in the Journal of Biomedical Sciences determined that the autoimmunity to the central nervous system may play a causal role in autism. Researchers discovered that because many autistic children harbour elevated levels of measles antibodies, they should conduct a serological study of measles-mumps-rubella (MMR) and myelin basic protein (MBP) autoantibodies. They used serum samples of 125 autistic children and 92 controlled children. Their analysis showed a significant increase in the level of MMR antibodies in autistic children. The study concludes that the autistic children had an inappropriate or abnormal antibody response to MMR. The study determined that autism could be a result from an atypical measles infection that produces neurological symptoms in some children. The source of this virus could be a variant of MV, or it could be the MMR vaccine.

6. Study published in the Annals of Clinical Psychiatry  suggests that Autism is likely triggered by a virus, and that measles virus (MV and/or MMR vaccine) might be a very good candidate. It supports the hypothesis that a virus-dincued autoimmune response may play a causal role in autism.

7. A study published in the American Journal of Clinical Nutrition determined that an increased vulnerability to oxidative stress and decreased capacity for methylation may contribute to the development and clinical manifestation of autism. It’s well known that viral infections cause increased oxidative stress. Research suggests that metals, including those found in many vaccines are directly involved in increasing oxidative stress.

8A study published by the Department of Pharmaceutical Sciences at Northeastern University, Boston determined that a novel growth factor signalling pathway that regulates methionine synthase(MS) activity and thereby modulates methylation reactions. The potent inhibition of this pathway by ethanol, lead, mercury, aluminum and thimerosal suggests that it may be an important target of neurodevelopmental toxins. You can read more about this here, and here.  You can read more about the MS/autism link here

9A study published in the Journal of Child Neurology examined the question of what is leading to the apparent increase in autism. They expressed  that if there is any link between autism and mercury, it is crucial that the first reports of the question are not falsely stating that no link occurs. Researchers determined that a significant relation does exist between the blood levels of mercury and the diagnosis of an autism spectrum disorder.

10. A study published in the Journal of Child Neurology noted that autistic spectrum disorders can be associated with mitochondrial dysfunction. Researchers determined that children who have mitochondrial-related dysfunctional cellular energy metabolism might be more prone to undergo autistic regression between 18 and 30 months of age if they also have infections or immunizations at the same time.

11. A study conducted by Massachusetts General Hospital at the Centre for Morphometric Analysis by the department of Paediatric Neurology illustrates how autistic brains have a growth spurt shortly after birth and then slow in growth a few short years later. Researchers have determined that neuroinflammation appears to be present in autistic brain tissue from childhood through adulthood. The study excerpt reads:

Oxidative stress, brain inflammation and microgliosis have been much documented in association with toxic exposures including various heavy metals. The awareness that the brain as well as medical conditions of children with autism may be conditioned by chronic biomedical abnormalities such as inflammation opens the possibility that meaningful biomedical interventions may be possible well past the window of maximal neuroplasticity in early childhood because the basis for assuming that all deficits can be attributed to fixed early developmental alterations in net

12, A study conducted by the Department of Paediatrics at the University of Arkansas determined that thimerosal-induced cytotoxicity was associated with the depletion of intracellular glutathione (GSH) in both cell lines.  The study outlines how many vaccines have been neurotoxic, especially to the developing brain. Depletion of GSH is commonly associated with autism. Although thimerosal has been removed from most children’s vaccines, it is still present in flu vaccines given to pregnant women, the elderly and to children in developing countries.

13. A study published in the Public Library of Science (PLOS)  determined that elevation in peripheral oxidative stress is consistent with, and may contribute to more severe functional impairments in the ASD group. We know that oxidative stress is triggered by heavy metals, like the ones contained in multiple vaccines.

14. A study conducted by the University of Texas Health Science Centre by the Department of Family and Community Medicine determined that for each 1,000 Ib of environmentally released mercury, there was a 43% increase in the rate of special education services and a 61% increase in the rate of autism. Researchers emphasized that further research was needed regarding the association between environmentally released mercury and developmental disorders such as autism.

15. A study published in the International Journal of Toxicology determined that in light of the biological plausibility of mercury’s role in neurodevelopment disorders, the present study provides further insight into one possible mechanism by which early mercury exposures could increase the risk of autism.

16. A study published in the Journal of Toxicology and Environmental Health determined that mercury exposure can induce immune, sensory, neurological, motor and behavioural dysfunctions similar to traits defining or associated with ASDs. Based upon differential diagnoses, 8 of 9 patients examined were exposed to significant mercury from Thimerosal-containing vaccine preparations during their fetal/infant developmental periods. These previously normal developing children suffered mercury encephalopathies that manifested with clinical symptoms consistent with regressive ASDs. Evidence for mercury intoxication should be considered in the differential diagnosis as contributing to some regressive ASDs.

 17. A study published by the US National Library of Medicine conducted by the University of Texas Health Science Centre suspected that persistent low-dose exposures to various environmental toxicants including mercury, that occur during critical windows of neural development among genetically susceptible children, may increase the risk for developmental disorders such as autism.

18. A study conducted by the Department of Obstetrics and Gynaecology at University of Pittsburgh’s School of Medicine showed that Macaques are commonly used in pre-clinical vaccine safety testing. Collective Evolution does not support animals testing, we feel there is a large amount of evidence and research that already indicated the links to vaccines in which some animals have been used to illustrate. The objective of this study was to compare early infant cognition and behaviour with amygdala size and opioid binding in rhesus macaques receiving the recommended childhood vaccines. The animal model, which examines for the first time, behavioural, functional and neuromorphometric consequences of the childhood vaccine regimen, mimics certain neurological abnormalities of autism. These findings raise important safety issues while providing a potential model for examining aspects of causation and disease pathogenesis in acquired disorders of behaviour and development.

19. A study conducted by The George Washington University School of Public Health from the Department of Epidemiology and Biostatistics determined that significantly increased rate ratios were observed for autism and autism spectrum disorders as a result of exposure to mercury from Thimerosal-containing vaccines.

20. A study published in the Journal Cell Biology and Toxicology by Kinki University in Osaka, Japan determined that in combination with the brain pathology observed in patients diagnosed with autism, the present study helps to support the possible biological plausability for how low-dose exposure to mercury from thimerosal-containing vaccines may be associated with autism.

21.  A study published by the Journal Lab Medicine determined that vaccinations may be one of the triggers for autism. Researchers discovered that substantial data demonstrates immune abnormality in many autistic children consistent with impaired resistance to infection, activation of inflammatory responses and autoimmunity. Impaired resistance may predispose to vaccine injury in autism.

22A study published in the Journal Neurochemical Research determined that since excessive accumulation of extracellular glutamate is linked with excitotoxicity, data implies that neonatal exposure to thimerosal-containing vaccines might induce excitotoxic brain injuries, leading to neurodevelopmental disorders.

Sources:

All sources not listed below are listed throughout the article and highlighted. To view them, please click on them.

(1)http://investors.morningstar.com/ownership/shareholders-major.html?t=GSK

(2)http://finance.yahoo.com/q/mh?s=twx+Major+Holders

(3)http://finance.yahoo.com/q/mh?s=ge+Major+Holders

(4) http://finance.yahoo.com/q/mh?s=pfe+Major+Holders

(5)http://cid.oxfordjournals.org/content/48/4/456.full

(6) http://www.ebcala.org/unanswered-questions

(7)http://www.collective-evolution.com/2013/07/07/courts-rule-mmr-thimerosal-containing-vaccines-caused-autism-brain-damage/

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Awareness

The Power of Peppermint: 15 Health Benefits Revealed

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In Brief

  • The Facts:

    This article was written by Sayer Ji, founder of Greenmedinfo.com where it was originally published. Posted here with permission.

  • Reflect On:

    A favourite herbal medicine of the ancients, peppermint leaves have been found in Egyptian pyramids dating back to 1,000 BC. Modern scientific investigations have now confirmed that this remarkable plant has over a dozen healing properties.

In our continuing effort to educate folks to the vast array of healing agents found in the natural world around us, we are excited to feature peppermint, a member of the aromatic mint family that you may already have squirreled away somewhere in your kitchen cupboard. While most have experienced peppermint as a flavoring agent, or perhaps as a comforting cup of herbal tea, few are aware of its wide range of experimentally confirmed therapeutic properties.

The ancients certainly were aware of the mint family’s medicinal value, having been used as herbal medicines in ancient Egypt, Greek and Rome thousands of years ago.[i]  Dried peppermint leaves have even been found in several Egyptian pyramids carbon dating back to 1,000 BC.

Today, modern scientific investigations are revealing an abundance of potential health benefits associated with the use of different components of the peppermint plant, including aromatherapeutic, topical and internal applications.

Most of the human research on peppermint performed thus far indicates this plant has great value in treating gastrointestinal disorders, including:

  • Irritable Bowel Syndrome – Since the late 90’s it was discovered that enteric-coated peppermint oil capsules are safe and effective in the treatment of this increasingly prevalent disorder.[ii]  This beneficial effect extends to the pediatric community. In one children’s trial 75% of those receiving peppermint oil had reduced severity of pain associated with IBS within 2 weeks.[iii] Another 2005 trial in adults concluded that “Taking into account the currently available drug treatments for IBS Peppermint oil (1-2 capsules t.i.d. over 24 weeks) may be the drug of first choice in IBS patients with non-serious constipation or diarrhea to alleviate general symptoms and to improve quality of life.”[iv]  In another 2007 trial 75% of patients receiving peppermint oil saw an impressive 50% reduction of “total irritable bowel syndrome score.”[v] Most recently, a study published January of this year found that peppermint oil was effective in relieving abdominal pain in diarrhea predominant irritable bowel syndrome.[vi]
  • Colonic spasm – Peppermint oil has been studied as a safe and effective alternative to the drug Buscopan for its ability to reduce spasms during barium enemas.[vii] [viii]
  • Gastric Emptying Disorders – Peppermint has been found to enhance gastric emptying, suggesting its potential use in a clinical setting for patients with functional gastrointestinal disorders.[ix]
  • Functional dyspepsia – A 2000 study published in the journal Ailment Pharmacology and Therapy found that 90 mg of peppermint oil and 50 mg of caraway oil resulted in 67% of patients reporting “much or very much improved” in their symptoms of functional dyspepsia. [x]
  • Infantile Colic: A 2013 study found that peppermint is at least as effective as the chemical simethicone in the treatment of infantile colic.[xi]

Click here to save your spot and get instant access to GreenMedInfo founder Sayer Ji’s interview! 

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Other studied applications include

  • Breastfeeding Associated Nipple Pain and Damage: A 2007 study found that peppermint water prevented nipple cracks and nipple pain in breastfeeding mothers.[xii]
  • Tuberculosis: A 2009 study found that inhaled essential oil of peppermint was able to rapidly regress tuberculous inflammation, leading the authors to conclude: “This procedure may be used to prevent recurrences and exacerbation of pulmonary tuberculosis.”[xiii]
  • Allergic rhinitis (hay fever): A 2001 preclinical study found that extracts of the leaves of peppermint  inhibit histamine release indicating it may be clinically effective in alleviating the nasal symptoms of allergic rhinitis.[xiv]
  • Shingles Associated Pain (Post-Herpetic Neuralgia): A 2002 case study found that topical peppermint oil treatment resulted in a near immediate improvement of shingles associated neuropathic pain symptoms; the therapeutic effects persisted throughout the entire 2 months of follow-up treatment. [xv]
  • Memory problems: A 2006 study found that the simple aroma of peppermint enhances memory and increases alertness in human subjects.[xvi]
  • Chemotherapy-Induced Nausea: A 2013 study found that peppermint oil was found to be effective in reducing chemotherapy-induced nausea, and at reduced cost versus standard drug-based treatment.[xvii]
  • Prostate Cancer: Preclinical research indicates that peppermint contains a compound known as menthol which inhibits prostate cancer growth.[xviii] [xix]
  • Radiation Damage: Preclinical research indicates peppermint protects against radiation-induced DNA damage and cell death.[xx]  [xxi]
  • Herpes Simplex  Virus Type 1: Peppermint has been found to have inhibitory activity against acyclovir-resistant Herpes Simplex virus type 1.[xxii] [xxiii]
  • Dental Caries/Bad Breath: Peppermint oil extract has been found to be superiorto the mouthwash chemical chlorhexidine inhibiting Streptococus mutans driven biofilm formation associated with dental caries.[xxiv] [xxv] This may explain why powdered peppermint leaves were used in the Middle Ages to combat halitosis and whiten teeth.

Peppermint is actually a hybridized cross between Water Mint (Mentha aquatica) and Spearmint (Mentha spicata),[xxvi] the latter of which has also been researched to possess remarkable therapeutic properties, such as the ability to exert significant anti-androgenic effects in polycystic ovarian syndrome[xxvii] and ameliorating the related condition of mild hirsutism, marked by excessive hair growth in females.[xxviii]

Like all plant medicines, extreme caution must be exercised when using extracts and especially essential oils.  Also, remember that more is not always better. A recent study on the use of rosemary in improving cognitive performance in the elderly found that a lower ‘culinary’ dose (750 mg) was not only more effective in improving cognition (as measured by memory speed) than a higher dose, but the highest dose (6,000 mg) had a significant memory impairing effect.[xxix] This illustrates quite nicely how less can be more, and why an occasional nightly cup of peppermint tea may be far superior as preventive strategy than taking large ‘heroic’ doses of an herb only after a serious health problem sets in.


Resources

  • [i] A. Sustrikova, I. Salamon, Essential oil of peppermint (Mentha x piperita L.) from fields in Eastern Slovakia., 2004: Zahradnictvi Horticultural Science 31(1): 31-36
  • [xxvi] The Complete Illustrated Book of Herbs, Alex Frampton, The Reader’s Digest Association, 2009

Originally published: 2018-08-31

Articule updated: 2019-05-21


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Awareness

25 Reasons to Avoid the Gardasil Vaccine

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It has been 13 years since the U.S. Food and Drug Administration (FDA) supplied fast-tracked approval for Merck’s Gardasil vaccine—promoted for the prevention of cervical cancer and other conditions attributed to four types of human papillomavirus (HPV). The agency initially licensed Gardasil solely for 9- to 26-year-old girls and women, but subsequent FDA decisions now enable Merck to market Gardasil’s successor—the nine-valent Gardasil 9 vaccine—to a much broader age range—9 to 45 years—and to both males and females.

As a result of Gardasil’s expanding markets not just in the U.S. but internationally, the blockbuster HPV vaccine has become Merck’s third highest-grossing product, bringing in annual global revenues of about $2.3 billion. However, Gardasil’s safety record has been nothing short of disastrous. Children’s Health Defense and Robert F. Kennedy, Jr. have just produced a video detailing the many problems with the development and safety of Gardasil. Please watch and share this video so that you and others may understand why Mr. Kennedy refers to Merck’s methodologies as “fraudulent flimflams.”

What follow are 25 key facts about Gardasil/Gardasil 9, including facts about the HPV vaccines’ clinical trials and adverse outcomes observed ever since Merck, public health officials and legislators aggressively foisted the vaccines on an unsuspecting public.

Inappropriate placebos and comparisons

  1. A placebo is supposed to be an inert substance that looks just like the drug being tested. But in the Gardasil clinical trials, Merck used a neurotoxic aluminum adjuvant called AAHS instead of using an inert saline placebo.
  2. Among girls and women who received the vaccine and among girls and women who received AAHS, an astonishing 2.3% in both groups experienced conditions indicative of “systemic autoimmune disorders,” many shortly after receiving Gardasil.
  3. Multiple scientific studies associate aluminum not just with autoimmune diseases but with autism, Alzheimer’s disease, dementia and Parkinson’s disease as well as behavioral abnormalities in animals.
  4. Merck lied to study participants, falsely saying that the clinical trials were not safety studies, that the vaccine had already been found to be safe and that the “placebo” was an inert saline solution. [Source: The HPV Vaccine on Trial  (photo evidence, pp. 6 and 12).]
  5. When Merck conducted clinical trials for its next HPV vaccine formulation, Gardasil 9, it used Gardasil as the “placebo” in the control groups, again relying on the lack of an inert placebo to mask safety signals.
  6. The 500 micrograms of aluminum adjuvant (AAHS) in Gardasil 9 are more than double the amount of aluminum in Gardasil; this raises the question of whether Gardasil 9’s heavy reliance on the Gardasil trials for comparison is justifiable.
  7. The World Health Organization states that using a vaccine (rather than an inert substance) as a placebo creates a “methodological disadvantage” and also notes that it may be “difficult or impossible” to assess vaccine safety properly without a true placebo.

Inappropriate inclusion and exclusion criteria

  1. In the only Gardasil trial in the target age group (11- and 12-year-old girls) with a control group design, fewer than 1200 children received the vaccine and fewer than 600 served as controls. This single trial involving fewer than 1800 children set the stage for the vaccine’s subsequent marketing to millions of healthy preteens all over the world.
  2. The Gardasil clinical trials had numerous exclusion criteria. Not allowed to participate in the trials were people with: severe allergies; prior abnormal Pap test results; over four lifetime sex partners; a history of immunological disorders and other chronic illnesses; reactions to vaccine ingredients, including aluminum, yeast, and benzonase; or a history of drug or alcohol abuse—yet Merck now recommends Gardasil for all of these groups.

Inadequate monitoring

  1. Some of the study participants—but not all—were given “report cards” to record short-term reactions such as redness and itching. The report cards monitored reactions for a mere 14 days, however, and Merck did not follow up with participants who experienced serious adverse events such as systemic autoimmune or menstrual problems.
  2. Injured participants complained that Merck rebuffed their attempts to report adverse side effects. In numerous instances, Merck maintained that these “weren’t related to the vaccine.”
  3. Half (49.6%) of the clinical trial subjects who received Gardasil reported serious medical conditions within seven months. To avoid classifying these injuries as adverse events, Merck dismissed them as “new medical conditions.”
Annual deaths from cervical cancer in the U.S. are 2.3/100,000. The death rate in the Gardasil clinical trials was 85/100,000—or 37 times that of cervical cancer.

Cervical cancer risk-benefit ratio not worth it

  1. The median age of cervical cancer death is 58 years. Gardasil targets millions of healthy preadolescents and teens for whom the risk of dying from cervical cancer is practically zero. Interventions for healthy people must have a risk profile that is also practically zero.
  2. Annual deaths from cervical cancer in the U.S. are 2.3/100,000. The death rate in the Gardasil clinical trials was 85/100,000—or 37 times that of cervical cancer.
  3. With 76 million children vaccinated at an average cost of $420 for the three-shot Gardasil series, the cost of saving one American life from cervical cancer amounts to about $18.3 million dollars. By contrast, the value of a human life according to the Department of Health and Human Services’s (HHS’s) National Vaccine Injury Compensation Program is $250,000—the maximum amount that the government program will award for a vaccine-related death.
  4. According to Gardasil’s package insert, women are 100 times more likely to suffer a severe event following vaccination with Gardasil than they are to get cervical cancer.
  5. The chances of getting an autoimmune disease from Gardasil, even if the vaccine works, are 1,000 times greater than the chances of being saved from a cervical cancer death.
  6. Women in Gardasil clinical trials with evidence of current HPV infection and previous exposure to HPV had a 44% increased risk of developing cervical lesions or cancer following vaccination.
  7. Women who get the Gardasil vaccine as preteens or teens are more likely to skip cervical cancer screening as adults, mistakenly assuming that HPV vaccination is a replacement for screening and that the vaccine will eliminate all risk.
Since Gardasil came on the U.S. market in 2006, people have reported over 450 deaths and over 61,000 serious medical conditions from HPV vaccines to the Vaccine Adverse Event Reporting System.

Fertility effects

  1. Accumulating evidence points to Gardasil’s potentially severe adverse effects on fertility, including miscarriage and premature ovarian failure.
  2. Merck never tested the vaccine for fertility effects. However, Gardasil and Gardasil 9 clinical trials showed high spontaneous miscarriage rates of 25% and 27.4%, respectively—significantly higher than the background rates of approximately 10%-15% in this reproductive age group.
  3. Polysorbate 80 and sodium borate (Borax) are associated with infertility in animals. Both are Gardasil ingredients, and both were present in the one clinical trial protocol that professed to use a benign saline placebo.

Post-licensing

  1. In 2015, Denmark opened five new “HPV clinics” to treat children injured by Gardasil. Over 1300 cases flooded the clinics shortly after their opening.
  2. Since Gardasil came on the U.S. market in 2006, people have reported over 450 deaths and over 61,000 serious medical conditions from HPV vaccines to the Vaccine Adverse Event Reporting System (VAERS).
  3. Merck lied to VAERS about the case of Christina Tarsell’s death, falsely claiming that her doctor blamed a virus instead of Gardasil. [Source: The HPV Vaccine on Trial  (p. 144).]

The vaccine that should never have been licensed

As suggested in the conclusion to the 2018 book The HPV Vaccine on Trial, the rollout of Gardasil in 125 countries worldwide has illustrated—in an all-too-real and shocking manner—the phenomenon that prompted Hans Christian Andersen to write “The Emperor’s New Clothes.” Around the world, over 100,000 Gardasil-related adverse events have now been reported to the FDA and WHO, and accounts continue to multiply of “scandal, lawsuits, severe injuries, and deaths.” For almost 200 years, Andersen’s story has taught readers about the need to speak the truth, pay attention to evidence and listen to children. The rosy narrative manufactured for the dangerous Gardasil vaccine must not be allowed to hold sway any longer. It is time, in the words of the HPV Vaccine on Trial authors, to proclaim—loudly—that “the Emperor has no clothes.”

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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.

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Wikileaks: Ecuador is Being Run By “Criminals & Liars.” Assange’s Entire Legal Defense Given To The United States

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In Brief

  • The Facts:

    Three weeks before the U.S. deadline to file its final extradition request for Assange, Ecuadorian officials are travelling to London to allow U.S. prosecutors to help themselves to Assange's belongings.

  • Reflect On:

    How do the global elite have the right and power to do what they do to people like Julian Assange and Edward Snowden? Do we really live in a democracy when small groups of people in power can basically make decisions that go against the majority?

What’s happening with Julian Assange is heart-breaking. He’s a hero, just like Edward Snowden. Government secrets are kept, not to protect ‘national security’ as commonly claimed, but rather to protect political and corporate interests. After all, the United States is evidently run by a small group of corporations. These corporations have a huge influence when it comes to dictating government policy, and they do not like those who disclose their secrets. For years, Wikileaks has been leaking documents that’ve exposed major corruption within multiple governments, including the United States and basically the entire western military alliance. They’ve exposed that our world operates very differently than how it’s been presented, and they’ve never had to retract a single story. They exposed the invisible government, or “the real menace of Republic,” a term coined by John F. Hylan, former Mayor of New York City. Hylan has said that the “invisible government, which like a giant octopus sprawls its slimy legs over our cities, states and nation.” He exposes the ones “who virtually run the United States government for their own selfish purposes.”  (source)

Transparency is what Julian Assange is all about, and the American empire and even the global empire have been desperately trying to keep their secrets and prosecute anyone or anything that threatens their secrecy. That’s what this is all about. And they proved that with Chelsea Manning.

It’s not just people like Assange who are being demonized and hunted, it’s alternative media as well. The war on ‘fake news’ that’s been happening for the last little while has resulted in alternative media outlets being labeled as ‘fake’, even if they’re presenting credible information and sources. Any media outlet who even questions a controversial issue has been labeled as ‘wrong’ or ‘fake.’

What is happening to Assange is extremely unjust, and should serve as a massive ‘wake up’ call for anyone who isn’t already ‘awake.’ Truth and free press threaten the ability of the global elite to continue their cycle of creating problems and then proposing solutions in order to achieve their desired outcome. Some of the biggest leaks WikiLeaks has made were when they revealed the connections between terrorist organizations like Al-Qaeda and ISIS to the western military alliance, and more specifically to the US government. Current presidential candidate and Congresswoman at the time, Tulsi Gabbard, even introduced a bill to stop this from happening.

We saw arms deals and the funding/support of terrorist organizations that the US claimed to be fighting against. This is a great example of how the global elite funds and creates a problem in order to justify a desired outcome (in this case it was heightened national security measures back home to protect people from ‘the war on terror’ and justify their infiltration of another country for ulterior motives).

I could go deeper into this, but the bottom line is that the arrest of Julian Assange comes at the hands of the criminals around the globe he was exposing, and it’s ironic that they are using their power and influence over mainstream media to portray Assange as the one who needs to be put behind bars.

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The Latest Update On Assange

Below is the latest update from the Wikileaks team via a recent press release.

Three weeks before the U.S. deadline to file its final extradition request for Assange, Ecuadorian officials are travelling to London to allow U.S. prosecutors to help themselves to Assange’s belongings.

Neither Julian Assange nor U.N. officials have been permitted to be present when Ecuadorian officials arrive to Ecuador’s embassy in London on Monday morning.

The chain of custody has already been broken. Assange’s lawyers will not be present at the illegal seizure of his property, which has been “requested by the authorities of the United States of America.”

The material includes two of his manuscripts as well as his legal papers, medical records and electronic equipment. The seizure of his belongings violates laws that protect medical and legal confidentiality and press protections.

The seizure is formally listed as “International Assistance in Criminal matters 376-2018-WTT requested by the authorities of the United States of America.” The reference number of the legal papers indicates that Ecuador’s formal cooperation with the United States was initiated in 2018.

Since the day of his arrest on April 11, 2019, Mr. Assange’s lawyers and the Australian consul made dozens of documented demands to the embassy of Ecuador for the release and return of his belongings, to which they received no response.

Earlier this week the UN Special Rapporteur on Privacy, who met with Mr. Assange in Belmarsh prison on April 25, asked to be present to monitor Ecuador’s seizure of Assange’s property. Ecuador inexplicably refused the request, despite the fact that since 2003, Ecuador has explicitly committed itself to granting unimpeded open invitations for UN special rapporteurs to investigate any aspect of their mandate in Ecuadorian jurisdiction.

The seizure and transfer of Mr. Assange’s property to the U.S. is the second phase of a bilateral cooperation that in January and February saw Ecuador arranging U.S. interrogations of past and present Ecuadorian diplomats posted to the embassy of Ecuador in London while Mr. Assange was receiving asylum. The questioning related to the U.S. grand jury investigation against Assange and WikiLeaks. As part of phase one of the cooperation, the United States also asked Ecuador to provide documents and audiovisual material of Assange and his guests, which had been gathered during an extensive spy operation against Assange inside the embassy.

On Friday, President Lenin Moreno initiated a state of emergency that suspends the rights of prisoners to “inviolability of correspondence, freedom of association and assembly and freedom of information” through Executive Decree 741.

Kristinn Hrafnsson, Editor-in-Chief of WikiLeaks said:

“On Monday Ecuador will perform a puppet show at the Embassy of Ecuador in London for their masters in Washington, just in time to expand their extradition case before the U.K. deadline on 14 June. The Trump Administration is inducing its allies to behave like it’s the Wild West.”

Hrafnsson continued:

“Ecuador is run by criminals and liars. There is no doubt in my mind that Ecuador, either independently or at the behest of the US, has tampered with the belongings it will send to the United States.”

Baltasar Garzon, international legal coordinator for the defence of Julian Assange and WikiLeaks, said:

“It is extremely worrying that Ecuador has proceeded with the search and seizure of property, documents, information and other material belonging to the defence of Julian Assange, which Ecuador arbitrarily confiscated, so that these can be handed over to the agent of political persecution against him, the United States. It is an unprecedented attack on the rights of the defence, freedom of expression and access to information exposing massive human rights abuses and corruption. We call on international protection institutions to intervene to put a stop to this persecution.”

Lawyer for Mr. Assange, Aitor Martinez, whose confidential legal papers were photographed with a mobile phone by embassy workers as part of a spy operation against Mr. Assange in October 2018, said:

“Ecuador is committing a flagrant violation of the most basic norms of the institution of asylum by handing over all the asylee’s personal belongings indiscriminately to the country that he was being protected from–the United States. This is completely unprecedented in the history of asylum. The protecting country cannot cooperate with the agent of persecution against the person to whom it was providing protection.

Ecuador has now also refused a request by the UN Special Rapporteur on Privacy, Joe Cannataci, to  monitor and  inspect the cooperation measure. Ecuador’s refusal to cooperate with the UN Special Rapporteur defies the entire international human rights protection system of the United Nations. Ecuador will from now on be seen as a country that operates outside of the system of safeguards of rights that defines democratic countries.”

Ecuadorian defence attorney for Mr. Assange, Carlos Poveda, said:

“In the face of countless abuses, and acting on provisions in domestic legislation and international human rights instruments, the defence has challenged the execution of this measure. All applications have been rejected. While the prosecution office proclaims its commitment to human rights protections, there has been no transparency and the investigation is conducted in secret. Without justification, and absent of all legal criteria, the measure shows the interest in obtaining information that the United States can use to proceed with its flagrant persecution. Meanwhile Ecuador has hinted that it too intends to proceed with investigations. Meanwhile, to date our criminal complaints of espionage against Julian Assange remain unprocessed, despite the gravity of the facts reported.”

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