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Vaccine Safety Untested on Pregnant Women, But Big Pharma Not Liable for Vaccine Injuries to Unborn Children and Pregnant Mothers

We are here today because in 2016, Congress amended the 1986 National Childhood Vaccine Injury Act to add vaccines recommended by the CDC for routine administration to pregnant women to the Vaccine Injury Table. Congressional action was required to do it because the 1986 Act was not about vaccines recommended for adults or unborn babies developing in the womb. As stated in multiple congressional hearings between 1982 and 1986, the National Childhood Vaccine Injury Act was created by Congress for one purpose: to protect the availability and lower the costs of federally recommended vaccines for children that are state mandated for school attendance. Although this NPRM requests public comment on how the addition of this new maternal vaccination category should be formatted on the Vaccine Injury Table, the public is hampered from making informed comments because of knowledge gaps about the safety and effectiveness of administering vaccines to pregnant women and potential negative health outcomes for the unborn child developing in the womb. Various package inserts for these vaccines contain warnings such as “it is not known whether the vaccine can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity;” and “there are no adequate and well controlled studies in pregnant women;” and “available data on the vaccine administered to pregnant women are insufficient to inform vaccine associated risks in pregnant women;” and “the vaccine should be given to pregnant women only if clearly needed.” There is no single vaccine-related issue of more concern to Americans than protection of this internationally recognized human right for pregnant women, parents of minor children and adults of all ages, who are too often being threatened and sanctioned if they do not agree to receive all government recommended and mandated vaccines for which the pharmaceutical industry has had no product liability since 2011.

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Study: Black Seed Oil Relieves Pain Associated with Arthritis

Black cumin seed oil, technically known as Nigella Sativa or N. sativa, has been used for thousands of years for several maladies, disorders, and both infectious and non-infectious diseases, especially throughout ancient Mideast, Egypt, and Greece. Currently, black cumin seeds and oils (from the seeds) are used as traditional medicines in the Mideast as well as parts of Africa and Asia. It's principal and most abundant bioactive phytochemical ingredient is thymoquinone. In addition to the multitude of anecdotal reports demonstrating efficacy and safety, there has been a growing curiosity among modern medical researchers who have been researching black cumin seed oil’s thymoquinone for the past few decades. Two more studies have been added in 2018, both relating to black seed oil's ability to relieve arthritis. One was a review article and the other a human trial study.

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Robert F. Kennedy, Jr. Demands the Office of the Inspector General and Congress Investigate Fraud in Vaccine Court by Denying Autism Vaccine Injuries

Robert F. Kennedy Jr., Chairman of Children’s Health Defense (CHD), and Rolf Hazlehurst, parent of a vaccine-injured child, petitioned the Department of Justice (DOJ) Office of Inspector General (OIG), and the Senate and House Judiciary Committees today to investigate actions taken by federal personnel during the “Vaccine Court” Omnibus Autism Proceedings (OAP). Recently discovered evidence provided by Kennedy and Hazlehurst details obstruction of justice and appallingly consequential fraud by two DOJ lawyers who represented the Department of Health and Human Services (HHS) in 2007. These actions led to a denial of justice and compensation for over 5,000 families who filed claims of vaccine injury leading to autism in their children. The fraud by the two DOJ attorneys directly influenced the 2011 Bruesewitz v. Wyeth Supreme Court decision which all but shut the door forever for families seeking redress for vaccine injury in the civil court system. Since this miscarriage of justice, roughly one million children have been diagnosed with autism. An unknown percentage of these cases are the result of vaccine injury.

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Federal Funding Provides Incentives for States to Take Children Away from Families Even When No Abuse is Present

When Child Protective Services (CPS) takes children from a loving, non-abusive family, the parents, and sometimes grandparents, aunts, and uncles, often seek out information about what is happening. Many gravitate toward groups on social media that provide education and support for those fighting CPS for their children. As the confused parents try to sort out the information and learn how to get their children back, one question dominates their search: How can this happen in America? Federal legislation enshrined in CAPTA and ASFA provide federal funding to states for foster care. For too long, these legislative acts have enabled and incentivized states taking children from innocent parents who have committed no crime, who have not abused their children. By any definition this is human trafficking. It is time to cut off the flow of tax dollars for the destruction of families, and instead find ways to help and support families.

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Are Vaccine Manufacturers Concealing Deaths Caused by Vaccines by Manipulating Post-marketing Data?

National and international health agencies such as the Centers for Disease Control and Prevention (CDC), the European Medicines Agency (EMA) and the World Health Organization (WHO) routinely and emphatically claim that serious adverse events following vaccination are rare. Nowhere is officialdom’s minimization of vaccine risks more apparent than in these agencies’ position on vaccine-related deaths. The WHO, for example, states that “so few deaths can plausibly be attributed to vaccines that it is hard to assess the risk statistically.” Nevertheless, once regulators have deemed that a given vaccine is safe enough to be licensed and widely marketed, vaccine manufacturers are supposed to do just that—that is, continue to statistically assess a vaccine’s risks, including the risk of death—and regulators are supposed to carefully review the postlicensure data that pharmaceutical companies submit. A 2017 commentary by India-based physicians Jacob Puliyel and C. Sathyamala in the Indian Journal of Medical Ethics describes a shocking dereliction of duty on the part of regulators who were presented with vaccine data carefully tailored to obscure serious risks. Tackling concerns about infant deaths that have occurred following hexavalent vaccination in several European countries, the authors of the commentary show that GlaxoSmithKline (GSK) neglected to report to regulatory authorities that there was a statistically significant increased risk of sudden infant death in the four days after administration of its hexavalent vaccine—and the regulatory agency in question (the EMA) ignored the omission and accepted GSK’s apparently whitewashed data at face value.

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Study: Replacements for BPA in BPA-free Products Just as Toxic – Time for Non-toxic Hemp Plastics?

BPA or Bisphenol A is a type of synthetically produced plastic derived from processing natural hydrocarbon fuels such as coal and crude oil. It’s often used for making polycarbonate plastics and epoxy resins to coat the inner linings of metal food containers. BPA is a synthetic endocrine disruptor capable of creating hormonal imbalances by mimicking or partially mimicking hormones, especially estrogen, that can lead to certain cancers, neurological disorders, compromised immune systems, and cause fertility and gender issues with women and men. It was chemically created in the late 1800s but not used commercially until the plastic industry began using it during the 1950s. Concerns among health-conscious people have motivated food processors to claim their containers are "BPA free". But BPA substitutes, such as BPS and other bisphenol compounds are not mentioned when food and beverage processors make their BPA free claims. Scientists outside the plastics industry are raising concerns that BPS and other related biphenol compounds create the same hormonal issues as BPA.

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Bad Medical Advice: How Taking an Aspirin a Day for Reported Health Benefits Could Actually Kill You

A few decades ago, during the 1970s, "an apple a day keeps the doctor away" morphed to "an aspirin a day keeps heart attacks and strokes away." Not only does this not work as a preventative measure for cardiac arrest and strokes, the side effects to the gastrointestinal or GI tract range can be severe. This is not an opinion. Several studies and even the FDA have expressed concerns about this approach for a healthy heart. Aspirin depletes the body of life-saving nutrients, such as potassium, sodium, folic acid, iron, and vitamin C, leading to anemia, depression, diarrhea fatigue, suppression of the immune system, and elevated homocysteine, which is ironically a strong heart disease risk factor. Long-term, daily consumption of aspirin can lead to undetected internal bleeding in the GI tract, eventually causing ulcers or leading to other serious inflammatory gastrointestinal conditions, even Crohn's Disease.

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Illinois Teen Dies Three Weeks After Being Injected with HPV Gardasil Vaccine

Christopher Bunch, 14 years old, died on Aug. 14, 2018 of complications from a rare neurological disease called Acute Disseminated Encephalomyelitis (ADEM). The teenager began experiencing symptoms, including headaches, nausea and vomiting, on Aug. 6. He spent much of the next two days sleeping. Christopher had apparently received the HPV (human papillomavirus) vaccine Gardasil three weeks prior to his death. ADEM is a reported side effect of Gardasil. It is listed in the Gardasil package insert.

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Michigan Department of Health Tracking Student Vaccination Status in Violation of Federal Law

The group Michigan for Vaccine Choice has sent a letter to parents in Michigan informing them that the Michigan Department of Health and Human Services (MDHHS) and the Michigan Department of Education (MDE) are violating federal law (FERPA) by transferring private medical records about minor children, without the consent of their parents, regarding each student's vaccination status into a vaccine tracking database.

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How Many American Deaths Will the EPA be Responsible for Before They Ban Glyphosate Herbicide?

A California jury recently found Monsanto liable for a groundskeeper’s cancer, ordering the company to pay out $289 million. It was the first lawsuit that went to trial alleging that Roundup and other glyphosate-based weed-killers cause cancer. Other research shows that cancer may only be the tip of the iceberg in describing the toll this chemical is taking on our health. There have been hundreds of lawsuits filed against Monsanto alleging that glyphosate, the active ingredient in the Roundup herbicide, causes cancer, and now finally the courts are taking the claims seriously as a federal judge recently ruled that these cases can proceed to trial. The World Health Organization has labeled glyphosate a “probable carcinogen” and yet the US Environmental Protection Agency (EPA) says it isn’t—although we shouldn’t be surprised, given the crony ties that have been exposed between top EPA officials and the biotech industry. The EPA can’t be counted on to protect our health. How is this chemical possibly in the market? Tell the EPA to ban glyphosate!

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Investigative Report in Kentucky Reveals Corruption Still Exists in Foster Care as Children Die or Go Missing

The corruption in Kentucky Child Protection Services and Foster Care has been reported on extensively here at Health Impact News since 2015. A new report aired on Wave 3 News by investigative journalist John Boel reveals that corruption in the Kentucky Cabinet for Health and Family Services is apparently ongoing, as one child was allegedly murdered by his foster parent after being taken away from his family, and another foster parent is blowing the whistle on the abuses of Kentucky foster care where children go missing due to lack of oversight. The current investigation began in 2017, when 4-year-old Hunter Payton died in foster care, and his biological parents questioned the story put forward as to the cause of his death, which was reported to be an accident. “They told us it was an ‘unlikely’ injury,” Hunter’s mother April Payton said. “It doesn’t happen. Something hit him hard.” He had only been in foster care for 3 months. During that time, the parents allegedly complained to the state about bruising on their son, and they were apparently told several different stories about how he died in an accidental fall. As John Boel reports: "Months after our report, Billy Embry-Martin, 33, was charged with murder. The lawsuit accuses him and his husband, Travis Embry-Martin, of 'violent punishment, physical abuse and denial of food.' Billy Embry-Martin is free on bond awaiting a December trial on the murder charge."

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American Academy of Pediatrics Concerned About Unregulated Food Additives, but Not Vaccine Additives

In July, 2018, The American Academy of Pediatrics (AAP) released a policy statement titled, Food Additives and Child Health. The report begins by stating, “Our purposes with this policy statement and its accompanying technical report are to review and highlight emerging child health concerns related to the use of colorings, flavorings, and chemicals deliberately added to food during processing (direct food additives) as well as substances in food contact materials, including adhesives, dyes, coatings, paper, paperboard, plastic, and other polymers, which may contaminate food as part of packaging or manufacturing equipment (indirect food additives); to make reasonable recommendations that the pediatrician might be able to adopt into the guidance provided during pediatric visits; and to propose urgently needed reforms to the current regulatory process at the US Food and Drug Administration (FDA) for food additives." However, one important subject that the AAP doesn’t address is the toxins in pediatric vaccines. Mercury, the second most dangerous substance known to mankind is still in childhood vaccinations–influenza, meningitis, HIB, Tdap, and Td; aluminum, a neurotoxin, is in a plethora of vaccines including hepatitis A and B, DTaP, Td, HIB, HPV; formaldehyde a known carcinogen is found in DTaP, Td, Hepatis A, Hib, influenza, and Tdap. There are other toxic substances in many different vaccines. Our children are the most vaccinated young people on the planet. Unfortunately, our children are the sickest when compared to any major Western country. It is long overdue for the AAP to address the elephant in the room; toxic additives in childhood vaccines.

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Study: Splenda Not Completely Eliminated from Body – Leads to Weight Gain

Splenda advocates and defenders were given an inconvenient truth from a new study that put the brakes on Splenda’s parade of health claims for marketing purposes. Splenda is the brand name for sucralose. One of the health claims for this chemically-altered sucrose is that its molecules are inert, they don’t produce internal biochemical changes. And even though it sweetens much more efficiently than chemically-unaltered table sugar, it is completely eliminated from the body naturally after ingestion and not stored as fat or even used as energy. Therefore it is calorie free. This most current sucralose animal study turns the claim that it is not stored in the body completely upside down: “The average Splenda users should be informed that sucralose is accumulating in their bodies and that it forms metabolites whose effects are unknown. The long-range effects of sucralose are not understood. Furthermore, we already know that it has adverse biological effects,” stated study author Susan Schiffman, Ph.D. Interestingly, the fact that all the rats in the study gained weight counters claims of non-calorie weight loss that’s promoted with sucralose. The fact that metabolites are formed and detected proves that sucralose is not an inert substance. What those metabolites are, where they are stored, and what dangers they might create, has been addressed by this new study and other studies prior to 2018.

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My Name Is Not “Respondent Mother”: The Need for Judicial Reform in Child Welfare

Losing a child for any reason is one of the most devastating things that can ever happen to a parent. The process of dealing with Child Protective Services and family court, while never easy, often serves to dehumanize parents and children. Instead of serving to help families overcome challenges, the system creates further harm when it treats parents as though they are worthless. Not only are civil and constitutional rights violated routinely, but many parents find that the system seeks to strip them of their basic human dignity. Law professor Vivek Sankaran recognizes that the treatment of parents by the courts is counterproductive to goals of restoring the family and helping the children. Sankaran wrote a piece for the American Bar Association addressing these concerns, with suggestions that could be implemented by the courts when dealing with parents facing allegations by CPS.

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FDA Wants to Turn CBD Oil Into a Drug that Will Cost $32,500 as They Ban all Other CBD Oils

For years, consumers have benefitted from access to cheap, safe, and effective CBD oil supplements. But now the FDA says that CBD is a drug, not a supplement—a drug which will be sold for $32,500 a year. Legally the FDA could at any time remove all CBD supplements from the market, on its own volition, or if the drug company which holds drug market exclusivity requests FDA do so. Unless we change the rules, we may see a government-sponsored monopoly on CBD oil, and in the near future, additional monopolies on other cheap, safe, and effective supplements. This threat to affordable CBD oil shows how broken this system is. An opioid epidemic is ravaging our country, with drug overdose deaths surpassing car accident fatalities. People are addicted to and dying from FDA-approved drugs, yet the agency is poised to eliminate consumer access to a non-addictive, cheap, safe, and effective alternative in CBD oil—all so one drug company can charge tens of thousands of dollars for what currently costs a few dollars. The FDA will not protect us—they’re in on it! More drugs mean more user fees—more money—for the agency, so don’t expect the FDA to defend your access to supplements.

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Food Freedom Flourishes in Maine: Model for Other States?

Food freedom is flourishing in the State of Maine. A year after the governor of Maine signed “the Maine Food Sovereignty Act,” many Maine towns have responded to the new law by adopting ordinances that give their residents the legal right to sell food to one another without burdensome regulations. There are good reasons to permit farmers and home-based food processors such as bakers to sell food to their neighbors without oversight, but in most every state this is not permitted. It’s not about food safety, but about corporate control of the food system. On the day after the Maine Legislature approved the law in July of 2017, the US Department of Agriculture (USDA) contacted state officials and threatened to federalize Maine’s system of livestock slaughtering and processing facilities. This article takes an in-depth look at Maine’s Food Sovereignty Act, the threat raised by the US Department of Agriculture against that law, and provides guidance for people in other states who want to bring food freedom to their communities.

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Study: Virgin Coconut Oil Improves the Microbiome and Fights Diabetes

A new study published in the journal Plant Foods for Human Nutrition on August 31, 2018, with the title Beneficial Effect of Virgin Coconut Oil on Alloxan-Induced Diabetes and Microbiota Composition in Rats adds further proof that virgin coconut oil is a powerful remedy for diabetes. In this latest study, virgin coconut oil was shown to be beneficial to the microbiome by increasing probiotic bacteria, leading to better outcomes for those suffering with diabetes. This new research confirms what many have reported to us over the past 15 plus years, that virgin coconut oil is beneficial in overcoming both Type 1 and Type 2 diabetes. This new study offers a possible explanation as to how virgin coconut oil helps people with Type 1 diabetes without directly affecting insulin levels.

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Alabama Senior Citizen Medically Kidnapped and Forced onto Drugs Against Family Wishes

Just as Child Protective Services and a judge have almost omnipotent, unchecked power to decide unilaterally that the relationship between a parent and a young child is not worthy of being preserved, Adult Protective Services and a probate judge have the same power to sever the relationship between an adult child and their elderly parent. Sometimes the relationship has endured for longer than the judge and social worker combined have been alive, yet with the stroke of a pen, a senior citizen can be completely torn away from their own children. The wishes of the elder can be completely ignored, and documents assigning power of attorney to a trusted adult child can become meaningless. Medical and financial decisions are placed into the hands of a court-appointed guardian who is often a stranger to everyone in the family. Nancy Scott, a retired English teacher from south Alabama, wrote to Health Impact News describing the medical kidnapping of her 102-year-old mother, who is also a beloved retired schoolteacher known to her former students as "Ms. Gregory." St. Vincent's Hospital and the Alabama Department of Human Resources (DHR) seized custody of Marian (Gregory) Leonard in February 2018. She is being held against her will, forced by a Jefferson County, Alabama, court into Hospice care, even though she has no terminal illness or disease. She is elderly, but her mind is sound. She is being drugged against her will and has told her daughter that she doesn't want the drugs. Nancy has always enjoyed a close relationship with her mother, but she has not seen her since midsummer. At that time, Ms. Gregory begged to go home. She told Nancy: "If you don't get me out of here, they're going to kill me, and they're going to kill you."

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Should the CDC Oversee Vaccine Safety When They Purchase Over $5 Billion of Vaccines from Big Pharma?

The U.S. Centers for Disease Control and Prevention (CDC) is tasked by the U.S. Government with overseeing vaccine safety. They claim on their website: "The United States’ long-standing vaccine safety program closely and constantly monitors the safety of vaccines. A critical part of the program, CDC’s Immunization Safety Office identifies possible vaccine side effects and conducts studies to determine whether health problems are caused by vaccines. Data show that the current U.S. vaccine supply is the safest in history." However, the CDC is the largest purchaser of vaccines in the world, and their budget to purchase vaccines from pharmaceutical companies was over $5.1 BILLION in 2018, and is set to increase to over $5.4 BILLION in 2019. Can we trust the CDC to oversee vaccine safety with such a blatant conflict of interest?

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Get Your Flu Shot? DOJ Report From Vaccine Court Reveals Flu Shot is Most Dangerous Vaccine in U.S.

The 2018 push for the flu shot is now in full swing. Pharmacies are advertising enticing offers, including free flu shots with discounts on other products (CVS), and the opportunity to give a free flu shot to children in Africa (Walgreens). These retail outlets offer no-wait shots, making it appear to be as easy as purchasing candy or tissue paper in your visit to your local drug store. What these retail outlets will most likely fail to mention, however, is that according to the Department of Justice's quarterly reports listing compensations for injuries and deaths due to vaccines from the Vaccine Court, the flu shot is the most dangerous vaccine in the U.S. with crippling and fatal side effects. How many people taking advantage of "free" flu shots will know that there is a long list of debilitating side effects from the flu shot, as compensated by the U.S. Government in the federal Vaccine Court? These side effects include (among others): GBS - Guillain–Barré syndrome is a rapid-onset muscle weakness caused by the immune system damaging the peripheral nervous system. TM - Transverse myelitis is an inflammation of both sides of one section of the spinal cord. This neurological disorder often damages the insulating material covering nerve cell fibers (myelin). ADEM - Acute disseminated encephalomyelitis, or acute demyelinating encephalomyelitis, is a rare autoimmune disease marked by a sudden, widespread attack of inflammation in the brain and spinal cord. CIDP - Chronic inflammatory demyelinating polyneuropathy is a neurological disorder -- a condition that targets your body's nerves. MS - Multiple sclerosis is a demyelinating disease in which the insulating covers of nerve cells in the brain and spinal cord are damaged. SIRVA - SIRVA stands for “Shoulder Injury Related to Vaccine Administration.” SIRVA can lead to intense, prolonged pain, limited range of motion, and shoulder-related injuries such as Adhesive Capsulitis or Frozen Shoulder Syndrome. Myasthenia gravis is a long-term neuromuscular disease that leads to varying degrees of skeletal muscle weakness. Peripheral Neuropathy is damage to or disease affecting nerves, which may impair sensation, movement, gland or organ function, or other aspects of health, depending on the type of nerve affected. DEATH by the flu vaccine. All of these debilitating side effects were reported as being compensated in recent DOJ reports.

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