Vaccine News – CDC Frauds: Connections Between the DeStefano Paper and the Thorsen Affair

Vaccine overload disorder is sweeping the nation while MDs are calling it anything but what it really is
Tuesday, March 07, 2017 by: S.D. Wells
(Natural News) The accumulation of toxins in the human body has never been tested by the FDA, CDC or AMA. From heavy metal poisons to chemical pesticides, time is our greatest enemy as Americans pour on, consume and inject more and more chemicals every year, adding to the already chaotic overload of GMOs, fluoridated water, flu shots and the “recommended” CDC boatload of vaccines that have never been proven safe or effective.
Are you experiencing brain fog, migraine headaches, severe allergies to foods, central nervous system disorders, anxiety, muscle spasms, immune system malfunctions, chronic inflammation or fibromyalgia? What you may really have is called Vaccine Overload Disorder, but no MD in America is allowed to speak of it, for fear of losing their license to practice medicine.
You should fear today’s vaccines more than you do infectious diseases – here’s why
Less than 65 years ago, U.S. pharmaceutical companies hired Nazi scientists right out of prison to work on vaccines and prescription drugs for Americans. The first polio vaccine, the “inactivated” version, was “invented” by Jonas Salk in 1955. Or was it? The true history shows us that Salk did nothing more than conduct illegal medical experiments on mental patients, and he had nothing at all to do with the decline in mortality from infectious diseases. In 1961, Albert Sabin developed the commercialized oral polio vaccine. Or did he? Did you know that historical data was altered by the corrupt vaccine industry to convince people that vaccines ended polio?
Be very afraid of the experimental toxins in every vaccine used in America – they are not “safe and effective”
Millions of Americans have been literally injected with cancer via vaccines, but it’s never mentioned by doctors who fear that the AMA, FDA and CDC will shut them down. Today’s vaccines not only contain live versions of the diseases you do not want, but also contain GMOs, hormones from infected cows, pigs, chickens and monkeys, untested virus combinations (like H1N1), aluminum, mercury, emulsifiers, and crossbred bacteria from animals, mosquitoes and diseased humans.
Most Americans have no clue that the live measles virus vaccine contains gelatin, sorbitol, sodium chloride, bovine cow serum, egg protein and human albumin.
Most Americans have no idea that the combination Diptheria, Tetanus and Polio Vaccine contains formaldehyde, phenoxyethanol and aluminum phosphate.
Hardly a living American has read the vaccine insert to know that the combination immunization jab DTaP, IPV, HBV and Hib given to infants 2 to 12 months young contains aluminum hydroxide, formaldehyde and bovine cow serum.
Who has ever been warned by their doctor or nurse that Gardasil HPV vaccine – the human papillomavirus vaccine made by Merck – contains polysorbate 80, sodium chloride, aluminum and a “denatured” (fragmented and weakened) form of the virus?

The debate is over: The MMR vaccine can cause Autism, and the CDC is engaged in a criminal conspiracy to cover up this fact.
By DrBuckley
Well, we now have proof that the chief authors of the 2004 study, including executives within the CDC, which alleged no link between the MMR vaccine and autism, conspired to cook the data, in order to deny the link.  How do we know that?  One of the authors, Dr. William Thompson, of the Journal of Pediatrics 2004 research paper which alleged no link between MMR and autism has come forward and made a confession to Dr. Brian Hooker, a confession which we now have a recording of.
In summary, here’s what we know:
Executives at the CDC, Dr. Frank Stefano, in particular,  knowingly excluded data from a key research paper which apparently refuted a link between autism and the MMR vaccine.  Dr. William Thompson has made a public statement admitting that his phone conversations were recorded, and has not denied anything which Dr. Hooker has leaked to the public about his confession.(2)
The data, had it been included in the final paper, indicated a 300% increase in autism amongst African American children. (3)
The CDC has sat on the evidence of a link between autism and the MMR vaccine for at least 10 years, and has continued to recommend the MMR vaccine for all children, injuring thousands in the process in their criminal negligence.

The 2004 CDC Study: Age at First Measles-Mumps-Rubella Vaccination in Children With Autism and School-Matched Control Subjects: A Population-Based Study in Metropolitan Atlanta
Results. The overall distribution of ages at MMR vaccination among children with autism was similar to that of matched control children; most case (70.5%) and control children (67.5%) were vaccinated between 12 and 17 months of age. Similar proportions of case and control children had been vaccinated before 18 or before 24 months. No significant associations for either of these age cutoffs were found for specific case subgroups, including those with evidence of developmental regression. More case (93.4%) than control children (90.6%) were vaccinated before 36 months (OR: 1.49; 95% confidence interval: 1.04–2.14 in the total sample; OR: 1.23; 95% confidence interval: 0.64–2.36 in the birth certificate sample). This association was strongest in the 3- to 5-year age group.
Conclusions. Similar proportions of case and control children were vaccinated by the recommended age or shortly after (ie, before 18 months) and before the age by which atypical development is usually recognized in children with autism (ie, 24 months). Vaccination before 36 months was more common among case children than control children, especially among children 3 to 5 years of age, likely reflecting immunization requirements for enrollment in early intervention programs.

CDC Frauds: Connections Between the DeStefano Paper and the Thorsen Affair.
By John Stone
Last week a Centers for Disease Control employee, William Thompson, came forward as whistleblower to admit that a 2004 study led by Frank DeStefano, of which Thompson himself was co-author was fraudulent, disguising the fact that incidence of autism was three and a half times higher in African Americans vaccinated with MMR before 36 months. In this light it is interesting that another co-author of the study, Marshalyn Yeargin-Allsopp, also liaised with Poul Thorsen over commissioning the equally fraudulent Madsen MMR/autism study. Thorsen who coordinated a series of studies between the CDC and Aarhus University/Staaten Serum Institut, Denmark was indicted in 2011 in the US on 13 counts of wire fraud involving the CDC and 9 of money laundering , but no attempt has been made to extradite him from Denmark.
None of the studies coordinated and co-authored by Thorsen have ever been retracted. At a congressional hearing in 2012 Coleen Boyle, another CDC employee and another co-author of the fraudulent DeStefano paper, failed to give straight answers when questioned by congressman Posey about Thorsen. Boyle could only recall two studies co-authored by Thorsen when in fact there were at least 21. On that occasion Congressman Posey memorably referred to Thorsen as “a humongous scum bag and one of the most wanted men on earth” .
If Cochrane 2005 smelt a rat with DeStefano 2004:
The conclusion, however, implied bias in the enrollment of cases which may not be representative of the rest of the autistic population of the city of Atlanta, USA where the study was set.
it actually stated there was a rat in the case of Madsen:
The follow up of diagnostic records ends one year (31 Dec 1999) after the last day of admission to the cohort. Because of the length of time from birth to diagnosis, it becomes increasingly unlikely that those born later in the cohort could have a diagnosis.

CDCs Dr. Coleen Boyle Suggested Manipulating Autism Dx Age in 2000
CDC’s Dr. Coleen Boyle who presented at the autism hearing today is one of the major architects of the the perpetuation of the autism epidemic. In April 2000, 6 weeks before the Simpsonwood meeting, Boyle suggested manipulating the data by adding 1 and 2 year olds to the data set – kids too young to have an ASD diagnosis – in order to dilute the danger. She belongs in prison. See the full email below (esp. #2).
Tuesday, April 25, 2000 3:55 PM
E-mail by Coleen Boyle to Frank DeStefano Cc to Tom Sinks.
Subject: comments of analysis
… “2. Since most of the dx’s are generally not picked up until the 2nd or 3rd year of life had you considered eligibility criteria of at least 18 months or 2 years?? What happens if you do this?” ….

Australian Prime Minister and Wife Tied to Pharma, Pushing Mandatory Vaccination
Mar 7, 2017
Australia’s politicians are deeply tied to pharmaceutical corporations, the British Monarchy, and other corporate and institutional powers which threaten the freedom and prosperity of Australian citizens.
One product of this hegemony is Australia’s “No Jab No Pay” law, which strips welfare from citizens who refuse vaccination for themselves or their children.
You could say people should just go without government welfare, and that’s a good idea for participants in the philosophy of independence from the system (Voluntaryism or Agorism), but the “system” in Australia has been constructed to make it difficult for anyone who is left out.
They can use this as leverage to cut off other necessities from citizens who refuse vaccination.
Without regard for the world of evidence for why people should not vaccinate, politicians and mainstream media speak of “improving vaccination rates.”
In its full perspective, No Jab No Pay is an eventuality when you see who holds power in the country. Let’s start with the Australian Prime Minister, Malcolm Turnbull.
He’s a multi-millionaire, with a chairman of a pharma corporation (who works with Novartis and GlaxoSmithKline) for a wife.
According to Money Morning:
“Australia’s new prime minister is a wealthy man. Last night, much was made of the fact that he doesn’t need to be in public life to have power and financial reward. He’s already amassed quite a fortune. Even before he entered politics. Various sources estimate his net worth at between $180 million and $200 million.”
In the mid 90’s, Turnbull invested 500,000$ in OzEmail and returned with about $60 million.
He wasn’t a good actor in response to questions about his finances, saying:
“When I was in business I did best out of start-ups. But OzEmail was a long time ago… I can’t live off my OzEmail laurels forever.’ ‘I don’t have private equity investments any longer because a) I’m in Parliament and b) I don’t have the time… Since I’ve been in Parliament my investments are rather limited. It’s all there on the record. It’s very boring and passive.”
Similar to how ex-FDA commissioner Margaret Hamburg’s husband owns a hedge fund called Renaissance Technologies, which owned stake in pharmaceutical companies she failed to properly regulate, the Australian Prime Minister and his wife Lucy Turnbull get rich together.
While the Prime Minister leads government, and pushes for mandatory vaccination to the benefit of pharmaceutical companies, his wife Lucy is chairman of the pharma corporation Prima Biomed.
CVac, the “cancer vaccine” is a main product of this corporation, still not seeing success. As we have exposed in past articles, figures in academia and government hype cancer causing viruses over avoiding carcinogens and general good health to profit from vaccination.

Vaccine News – Did Chinese scientists find autism’s missing puzzle piece?

Would You Want Your Vaccine Produced by Supporters of Jihad?
by Judith Bergman
February 25, 2017 at 5:00 am
“Selling the crucial manufacture of vaccines to an ideologically hostile country, which might – for whatever reason – suddenly decide to shut down production, does not sound like a good idea… Those who say that the Saudis are merely interested in profit, just like everybody else, should know better”. — Rachel Ehrenfeld, expert on financing terrorism
Virtually all political parties supported the Danish government’s sale of its vaccine manufacturing facility to the Saudi conglomerate.
After the publication of the Danish Mohammad cartoons in 2006, Saudis boycotted Danish goods. Do Danish politicians really have such short memories?
Vaccines are not an easy commodity to come by. It takes minimum six months for an order of vaccines to be delivered, but, according to the World Health Organization, delivery can also easily take up to two years.
How much trust are Danish consumers supposed to have in a Saudi owned conglomerate, which employs jihadists such as Usmani and donates heavily to jihadist organizations such as the Muslim Brotherhood, who want to bring about a caliphate? The potential for political exploitation is too evident to reject.
Would you want your vaccines produced by a Saudi company that supports jihad? Danes, it seems, may have no choice.

Did Chinese scientists find autism’s missing puzzle piece?
BY J.B. HANDLEY February 22, 2017
Discovery #1: “Maternal Immune Activation” can cause autism
Further Refinement of Discovery #1: Immune Activation from the Cytokine Interleukin-6
Dr. Patterson: what can cause immune activation?
Aluminum hydroxide, aka “aluminum adjuvant”.
Discovery #2: Aluminum Adjuvant causes immune activation and is far more neurotoxic than previously thought
The scientific understanding of aluminum adjuvant toxicity has changed and deepened dramatically in recent years (since 2007).
Discovery #3: Aluminum can increase IL-6 in the brain
The evidence for post-natal autism triggers is strong
Discovery #4: Hepatitis B vaccine induces IL-6 in postnatal rats
This new study demonstrates that vaccines can affect brain development via immune activation. Hence, the immune activation experiments are relevant to vaccines…The hep B vaccine increased IL-6 in the hippocampus (the only brain region analyzed for cytokines).”
“Aluminum increased the intensity and duration of macroscopic and histologic inflammation, colonic myeloperoxidase activity, inflammatory cytokines expression, and decreased the epithelial cell renewal compared with control animals. Under basal conditions, aluminum impaired intestinal barrier function. In vitro, aluminum induced granuloma formation and synergized with lipopolysaccharide to stimulate inflammatory cytokines expression by epithelial cells. Deleterious effects of aluminum on intestinal inflammation and mucosal repair strongly suggest that aluminum might be an environmental IBD risk factor.”
“With the discovery of autoimmune/inflammatory syndrome induced by adjuvants (ASIA), the work of leading researchers from 14 countries on the role of adjuvants in different vaccines and how they can induce diverse autoimmune clinical manifestations in genetically prone individuals has been published in the newly released medical textbook, Vaccines and Autoimmunity.”
Mercury in vaccines is dangerous and unjustifiable based on published science. It should be removed from 100% of vaccines immediately.
Synergistic toxicity means that mercury combined with aluminum may be 100x more toxic than either metal by itself, we don’t really know:
“How can 1 + 1 = 100? ‘Synergistic toxicity’ refers to the effect that when exposed to two toxins, the toxicity level is far greater than the additive toxicity levels of the two toxins.”
There are many anecdotal stories that children diagnosed with autism today are “less severe.” Is this true? Is the removal of mercury the reason? There’s no data I can find to support this, so it’s just conjecture for the moment.
However, IF the core hallmark of triggering autism is an immune activation event, than aluminum adjuvant is more likely the central cause, and this matches the reality that autism rates have continued to rise after the removal of MOST mercury from vaccines. Mercury is NOT an immune system antagonist the way aluminum adjuvant is, mercury was in vaccines for its effectiveness as an antibacterial and an anti fungal, not an adjuvant.
VP has very strong opinions about the mercury vs. aluminum adjuvant debate, including this: “There are far more important issues than mercury, such as aluminum adjuvant neurotoxicity, and immune activation injury.”
The most obvious answer is that the MMR vaccine is the first live virus vaccine children receive (it’s typically given between age 12–18 months, most children have received 15–20 vaccines by then), and it’s a triple (measles, mumps, rubella) live virus. For an immune system bathed in aluminum adjuvant and possibly already simmering with activation events, this triple dose might push a child right over the edge. This might explain the seizures (an extreme immune activation event) that sometimes follow the MMR appointment. We also know that children who also receive the varicella vaccine (chicken pox) along with the MMR have higher rates of seizure events. This would make sense, four live viruses at once would likely challenge the immune system more than three, but we can’t explain exactly how the MMR biologically impacts the immune system the way we can for aluminum adjuvant, and now for Hepatitis B vaccine (thanks to Chinese scientists). Dr. Yehuda Shoenfeld discusses the fact that a live vaccine activates the immune system more than a vaccine using aluminum adjuvant:
“It is evident that a live attenuated vaccine is more prone than a killed vaccine to activate the immunity response.”
Question: Didn’t they already prove vaccines don’t cause autism?
No vaccine containing aluminum adjuvant has ever been explored for its relationship to autism, despite a growing and clear body of evidence implicating aluminum adjuvant in causing “immune activation,” the central cause of autism.

Hidden Laws and Guidelines on Informed Consent Could Protect Children Against Mandatory Vaccination
Recently, new laws have emerged surrounding the issue of informed consent, both in the UK and the US. However, very few of us know that these laws exist. We believe that this is because these laws have the potential to protect children against mandatory vaccination.
In the UK, a recent ruling titled The Montgomery Ruling states that a patient must have sufficient information to make an informed choice about any medical treatment that is being offered to them.
In 2015, the website Medical Protection, which outlined this ruling, stated that:
“The patient must have sufficient information to make a choice – without adequate information, patients are unable to make decisions about their treatment. The information provided should, for example, include: an explanation of the investigation, diagnosis or treatment; an explanation of the probabilities of success, or the risk of failure; or harm associated with options for treatment. The patient should be given time to ask questions. The GMC and the courts expect patients to be given all information material to their decision, with the proviso that it would not cause the patient serious harm.”
They continued:
“The patient must be able to give their consent freely – pressuring patients into consenting to treatment invalidates the consent. To ensure that consent is freely given, patients should, where possible, be given time to consider their options before deciding to proceed with a proposed treatment. Be aware, too, that patients’ friends and relatives may also try to exert their influence and that this can be subtle but nevertheless powerful.”
This ruling, which was made following the case of Montgomery v Lanarkshire Health Board, has huge implications surrounding the health and safety of hundreds of thousands of children, not only in the UK but worldwide.

Consent – The basics
15 May 2015
Summary
Respect for patients’ autonomy is expressed in consent law; to impose care or treatment on people without respecting their wishes and right to self-determination is not only unethical, but illegal.
Key principles
For consent to be valid:
The patient must be competent – mental capacity is decision-specific. Assessment of a person’s capacity should be based on his/her ability to understand, retain and weigh in the balance the information relevant to a particular decision. The person must also be able to communicate the decision. A patient who is unable to make a decision about a complex proposal is not necessarily incapable of making any decisions at all, and may be perfectly able to consent where the issues are simpler. The starting point in the case of adults is always to presume that the patient has capacity until it is shown otherwise.
The patient must have sufficient information to make a choice – without adequate information, patients are unable to make decisions about their treatment. The information provided should, for example, include: an explanation of the investigation, diagnosis or treatment; an explanation of the probabilities of success, or the risk of failure; or harm associated with options for treatment. The patient should be given time to ask questions. The GMC and the courts expect patients to be given all information material to their decision, with the proviso that it would not cause the patient serious harm.
The patient must be able to give their consent freely – pressuring patients into consenting to treatment invalidates the consent. To ensure that consent is freely given, patients should, where possible, be given time to consider their options before deciding to proceed with a proposed treatment. Be aware, too, that patients’ friends and relatives may also try to exert their influence and that this can be subtle but nevertheless powerful.

JUDGMENT – Montgomery (Appellant) v Lanarkshire Health Board (Respondent)(Scotland), source: https://www.supremecourt.uk/decided-cases/docs/UKSC_2013_0136_Judgment.pdf

Autism’s Gut-Brain Connection By Melissa Pandika
Groundbreaking research suggests that a treatment for autism may come in the form of a probiotic.
Stress can send your stomach into a painful tailspin, causing cramps, spasms and grumbling. But trouble in the gut can also affect the brain.
This two-way relationship may be an unlikely key to solving one of medicine’s most pressing — and perplexing — mysteries: autism. Nearly 60 years after the disorder was first identified, the number of cases has surged, and the United Nations estimates that up to 70 million people worldwide fall on the autism spectrum. Yet there is no known cause or cure.
The gut bacteria in individuals with autism aren’t just different… they may actually contribute to the disorder.
But scientists have found promising clues in the gut. Research has revealed striking differences in the trillions of bacteria — a.k.a., the microbiome — in the intestines of children with and without autism. But the gut bacteria in individuals with autism aren’t just different. Researchers at the California Institute of Technology have shown for the first time that they may actually contribute to the disorder. They reported in the journal Cell in December 2013 that an experimental probiotic therapy alleviated autism-like behaviors in mice and are already planning a clinical trial.
Today autism is treated primarily through behavioral therapy. But the new study suggests that treatment may one day come in the form of a probiotic — live, beneficial bacteria like those found in yogurt. “If you block the gastrointestinal problem, you can treat the behavioral symptoms,” Paul Patterson, a professor of biology at Caltech who co-authored the study told SFARI.org. University of Colorado Boulder professor Rob Knight hailed the finding as “groundbreaking” in a commentary in Cell.
Autism is a complex spectrum of disorders that share three classic features — impaired communication, poor social engagement and repetitive behaviors. On one end of the spectrum are people who are socially awkward but, in many cases, incredibly sharp. At the other extreme are individuals with severe mental disabilities and behavioral problems.
Treatment for autism may one day come in the form of a probiotic — live, ’friendly’ bacteria like those found in yogurt.
Among the most common health complaints from children with autism? Gastrointestinal problems. Although estimates vary widely, some studies have concluded that up to 90 percent of children with autism suffer from tummy troubles. According to the CDC, they’re more than 3.5 times more likely to experience chronic diarrhea and constipation than their normally developing peers.

Natural News – HuffPost, Slate and Salon all part of a massive vaccine cover-up “conspiracy of silence” to keep poisoning children with mercury
Sunday, February 26, 2017 by: Ethan Huff
(Natural News) The refusal of mainstream media outlets to report on or investigate vaccine safety issues is nothing new: it’s been like this for a long, long time, and is hardly a surprise to anyone who’s been paying attention to the official narrative for any substantial period of time. But now some “alternative” media outlets like the Huffington Post, Slate, and Salon are doing the exact same thing, aiding and abetting the enemy in keeping things like toxic mercury in childhood vaccines.
As part of his World Mercury Project challenge, Robert F. Kennedy, Jr., recently gave a speech at the National Press Club Conference in which he addressed the issue of vaccine safety before a room full of reporters. Among other things, Kennedy talked about how vaccine safety under the current paradigm is a joke, especially when it comes to the continued use of a known mercury-based neurotoxin known as Thimerosal that is still used in influenza and various other vaccines administered to children.
During his speech, Kennedy, who recently met with President Trump about heading a new vaccine safety committee, took aim at journalists who refuse to look into the matter more deeply — which is their job on behalf of the public interest. Rather than honestly investigating the matter, they capitulate to the politically-correct notion that all vaccines are 100 percent safe and effective, and anyone who questions this is a science-denying quack.
“The so-called ‘alternate’ press, which is supposed to be the antidote to the corporate control of our media … they won’t run any kind of debate or criticism of this issue,” says Kennedy. “There’s something wrong with that in democracy that the press, which is the final readout for public scrutiny of institutions and industry, has been completely removed from this debate.”
“You cannot go on TV and talk about this. You cannot go to the press. You will be maligned; you will be marginalized as ‘anti-vax.’”

Over-vaccinating and the overdosing of pet vaccines has become a global issue. 5 lbs dogs are receiving the same dose of the rabies vaccine as 150 lbs Great Danes, and vets are now witnessing terrible side effects.

11 Reasons Why Flu Shots Are More Dangerous Than The Flu Itself

1. The flu shot actually makes you sick to begin with
2. Flu vaccines contain other dangerous ingredients such as mercury
3. The flu shot can cause Alzheimer’s disease
4. The very people pushing flu vaccinations are making billions of dollars each year
5. Lack of real evidence that young children even benefit from flu shots
6. Makes you more susceptible to pneumonia and other contagious diseases
7. Vascular disorders
8. Children under the age of 1 are at risk
9. Increased risk of narcolepsy
10. Weakens immunological responses
11. Serious neurological disorders

Sources for this article include:
Study Again Finds Narcolepsy Risk With H1N1 Flu Vaccine
Inflammatory Response After Influenza Vaccination in Men With and Without Carotid Artery Disease
Conflicts of Interest in Vaccine Policy Making
VRM: 5 Reasons Not To Get The Flu Shot
Is Your Child High-Risk for an Adverse Vaccine Reaction?
Natural Alternatives to the Flu Shot Prove Just as Effective

WIKILEAKS’ EMAIL LEAKS UNCOVER THE VATICAN’S POSSIBLE KNOWLEDGE OF EXTRATERRESTRIALS

WIKILEAKS’ EMAIL LEAKS UNCOVER THE VATICAN’S POSSIBLE KNOWLEDGE OF EXTRATERRESTRIALS
This time, it was John Podesta’s account, showing multiple emails from Dr. Edgar Mitchell, Apollo 14 astronaut, showing how Mitchell (1940-2016) had big plans, and big meetings set up.
Edgar Mitchell was very active in moving the “disclosure” process by discussing the matter with various contacts inside of the White House and Pentagon, along with the Disclosure Project’s Dr. Steven Greer.

Here is one of the emails that was recently released by Wikileaks, and it mentions the Vatican:

From:terribillionairs@aol.com
To: john.podesta@gmail.com
Date: 2015-01-18 19:34
Subject: email for John Podesta (c/o Eryn) from Edgar Mitchel re meeting ASAP
Dear John,
As 2015 unfolds, I understand you are leaving the Administration in February.
It is urgent that we agree on a date and time to meet to discuss Disclosure and Zero Point Energy, at your earliest available after your departure.
My Catholic colleague Terri Mansfield will be there too, to bring us up to date on the Vatican’s awareness of ETI.
Another colleague is working on a new Space Treaty, citing involvement with Russia and China. However with Russia’s extreme interference in Ukraine, I believe we must pursue another route for peace in space and ZPE on Earth.
I met with President Obama’s Honolulu childhood friend, US Ambassador Pamela Hamamoto on July 4 at the US Mission in Geneva, when I was able to tell her briefly about zero point energy.
I believe we can enlist her as a confidante and resource in our presentation for President Obama.
I appreciate Eryn’s assistance in working with Terri to set up our meeting.
Best regards,
Edgar
Edgar D. Mitchell, ScD
Chief Science Officer & Founder, Quantrek
Apollo 14 astronaut
6th man to walk on the Moon
PS Terri’s cousin by marriage and former Mayor of Chicago Jane Byrne died recently. Raum Emmanuel was at her funeral.

New Wikileaks’ Email Leaks Support Tom Horn / Steve Quayle Research Into Vatican Cover-Up Regarding “Extraterrestrials”—Role Church Will Play In Coming “Official Disclosure”

A 39-year-old British conspiracy theorist and UFO phenomenologist who was found dead in Warsaw in June sent his mother a text days before his death telling her, “If anything happens to me, investigate.”
Max Spiers, who was in excellent health according to his family, was discovered dead on a couch by a woman he was staying with ahead of a conference he was due to speak at in Poland. Polish authorities attributed the death to natural causes, but no post-mortem was performed at the time.
“I think Max had been digging in some dark places and I fear that somebody wanted him dead,” his mother, Vanessa Bates, told the Telegraph.
Scott C. Waring of UFO Sightings Daily told the Metro, “This is really strange. It does seem that UFO researchers are now being targeted, probably to slow the rate of information being leaked to the public.”

Video: http://www.sfgate.com/weird/article/UFO-hunter-texted-If-anything-happens-to-me-9976334.php?cmpid=fb-desktop

Why I won’t vaccinate

If you choose to read this, please read the whole thing.

So here it is, a little bit of why we no longer vaccinate, with reasoning for each particular vaccination before 12 years old:

As of 2016, a child in America is scheduled to received 74 vaccinations by the time they turn 18. With each shot, you are taking the risk of your child suffering the side effects, even as severe as SIDS, paralysis, deafness, blindness, and death. That’s 74 times… I just personally can’t agree to roll those dice with the lives and lifelong health of my children. With most shots, you are also allowing heavy metals to accumulate in their body.

I am extremely uncomfortable with the notion that as a duty to society, I must choose to inject known poisons into my child’s body. I will never be convinced again to stick a needle into my child containing recognized carcinogens, neurotoxins, and other poisons that can cross the blood-brain barrier and build up in my child’s body. When you put something like aluminum into the body by way of injection, it bypasses the protective mechanisms of the gastrointestinal tract, circulates in your body, and is deposited in your body tissues. *There are NO STUDIES that prove that the amount of aluminum in vaccines is safe to inject into an infant or a toddler (or human for that matter).*

Aluminum IS however known to cause neurological harm, degenerative problems, autoimmune disorders, and inflammatory conditions. Conditions that fall under these categories are: Lupus, Graves’ Disease, Lupus, Celiac Disease, Chronic Fatigue Syndrome, Chron’s Disease, Endometriosis, Fibromyalgia, Arthritis, Scleroderma, Vitiligo, Multiple Sclerosis, Muscular Distrophy, Cancer, Parkinson’s, Diabetes, Asthma, Irritable Bowel Syndrome, and more. These are debilitating ailments that a child can develop at any time and face for the rest of their lives. How can someone tell me as a mother that I need to do this to my child because “it’s best for everyone else?”

Other harmful ingredients and additives whose toxic effects have NEVER been examined by injecting them into small children are Formaldehyde, MSG, 2-Phenoxyethanol, and others.

Formaldehyde is a carcinogen, that is a fact. It can cause genetic damage and kidney damage if inhaled, but no one has bothered to study the effects of shooting it into our children with needles. Glutamate, a component of MSG, is an excitotoxin which is a chemical that affects brain function. They’ve taken MSG out of baby food, but left it in vaccines… 2-Phenoxyethanol is a chemical preservative used in perfumes, insect repellents, germicides, solvent for dyes, plasticizers, and antiseptics. It is harmful and can cause reproductive defects and severe skin and eye irritation if inhaled, swallowed, or absorbed through the skin. Again, despite this, it’s still in vaccines and the harm hasn’t been studied by way of injection. But let’s just assume they’re all safe, right?

Also to be considered is the use of any sort of human DNA such as aborted fetal cells. This can trigger autoimmune reactions. The immune system will attack the foreign human DNA, and this attack can then in turn become an attack against the child’s own body because it can’t tell the difference between same-species DNA. The injected human DNA inserts itself into the genes of the child and alters their genetic function. Animal substances are concerning as well, because when they are screened for disease, there is a possibility of missing animal viruses there are no tests for. This has happened before.

I can’t fathom routinely injecting poisons that I know are harmful and toxic into my child and taking the risk of life-long ailments. Yes, that means I am taking a bit of a higher risk of her catching a disease that vaccines may offer some protection against, but the risks are low, and *vaccinated children catch them too.* It is a FACT that certain toxic ingredients are cause harm, while it is only a possibility that my child may catch diseases we could vaccinate against. There are healthy ways to prevent and combat these diseases, and contracting and managing most of them will result in lifelong immunity.

What I’ve written below this are the chances of my child catching the diseases vaccines are supposed to protect against, and the risks that I feel outweigh the benefits of each vaccination. This includes the side effects of the shots and the harmful chemicals that they contain.

HIB: HIB is NOT a common disease. A breastfed child who does not attend daycare is at an even lower risk of catching it. The fatality rate of those who do catch it is 5%, usually when it is not caught soon enough. There are about 25 cases per year in the US, meaning the risk for my child to catch it in their first 2 years of life is about 1 in 200,000. After age 2, it’s nearly 0. It is also treatable. Concerning adverse reactions include seizures, encephalitis (brain swelling), autoimmune reactions, nervous system dysfunction, anaphalaxis, angiodema, apnea, hives, Guillain-Barré syndrome (GBS), convulsions, renal failure, and severe allergic reactions. The vaccine contains aluminum and formaldehyde, which I’ll explain the issues about later.

PC (Pneumococcus): 1/3 of severe cases of Pc are caused by strains NOT covered by the vaccine. The chances of a child by age 2 having a severe case is 1 out of 2850. Pc is treatable. Again, a breastfed child not in daycare is at low risk for catching this. Most infants suffer one or more systemic or local reactions with this shot. The more concerning adverse reactions in infants and toddlers during clinical studies included: DEATH (SIDS), bronchiolitis, gastroenteritis, pneumonia, SIDS, apnea, decreased limb mobility, arthritis, GBS, seizures, heart failure, pancreatitis/myocardial infarction resulting in death. This vaccine contains aluminum.

DTaP (Diphtheria, Tetanus, Pertussis): Diphtheria is extremely rare, at 5 cases per year and not a single one since 2003 in the US. The risk is basically 0. Tetanus is virtually unheard of in people under 5 years old, and there are only 10 cases per year in people 5-25 years of age. The risk is 1 in 500,000. Pertussis (Whooping Cough) is more common, but in my child’s first 12 years of life, their risk of having a severe case is 1 in 3333. Pertussis is rarely problematic after 1 year of age. Infection is likely to create life-long immunity. It is treatable. The fatality rate is 1% for infants and toddlers and adults do not die from it in the US. Reactions to this vaccine include: death, brain injury, coma, severe seizure disorders, GBS, Brachial neuritis (dysfunction of nerves in the arm), Cyanosis, anaphylactic shock, grand mal seizures, bronchitis, pneumonia, hypotonia, encephalopathy, apnea, SIDS, and autism. This contains aluminum, formaldehyde, polysorbate 80, glutaraldehyde, and 2-phenoxyethanol.

Hep B: This disease is also rare in children under 12. Virtually all cases of Hep B in infants each year are results of transmission by the mother at birth. Vaccinating for this actually began with attempts to control the disease by stopping it within high risk groups. When this didn’t work, they started vaccinating all newborns for it instead. There’s really no reason for an infant to get this shot if the mother is not infected. In the first 12 years of life, chances of contracting Hep B are 1 in 40,000, almost all passed on from the mother. SOME known reactions of this shot are: lupus, blood vessel inflammation, Stevens-Johnson Syndrome, liver damage, wheezing, hair loss, bruises, GBS, eczema , liver damage, asthma, heart palpitations, arthritis, anaphylaxis, severe nerve dysfunc. Paralysis, GBS, seizures, spinal cord inflammation, optic nerve inflammation, multiple sclerosis. This contains aluminum and formaldehyde.

Rotavirus: Most children who gets this don’t even know and recover from it just like any other common virus. When it becomes severe, it’s usually due to dehydration. Fatalities are rare. This vaccine is a live virus, meaning a child who gets the shot can pass the virus on to others or become infected themselves with Rotavirus (Rotavirus infection is a possible side effect). Common side effects mimic the virus itself. Worse reactions include: seizures, Kawasaki disease, intussusception (requiring emergency surgery), DEATH, SIDS, pneumonia, bleeding from low platelet counts, and hives. This vaccine contains monkey kidney cells, fetal cow blood, Polysorbate 80, and pig virus contaminants.

Polio: Polio doesn’t exist in the US, so in all reality my child is not in need of any protection this may offer. The vaccine can cause allergic reactions, anaphylactic shock, lymphadenopathy, convulsions, and other mild reactions. This shot contains baby cow blood serum, human proteins, Glutamate, formaldehyde, 2-phenoxyethanol, and monkey kidney cells.

MMR (Measles, Mumps, and Rubella): Severe cases of these diseases are so extremely rare that the risk is basically 0 for my child. Measles is not common, at 300 cases in the US per year (all ages of people) and complications are uncommon. Mumps is just as rare, and severe complications are almost nonexistent before puberty. Rubella does not cause severe illness in infants and children. There are only 20 cases per year. This is a live virus, so the vaccinated can spread Rubella following the shot. Known reactions include: Measles infection, aseptic Meningitis, arthritis, pancreatitis, pneumonia, severe eye inflammation that can permanently affect vision, nerve deafness in the ear, Stevens-Johnson Syndrome, panniculitis, vasculitis, pneumonia, pneumonitis (nonbacterial lung inflammation), and neurological reactions like brain swelling, GBS, ataxia (balance problems with difficulty walking), multiple nerve inflammation and dysfunction. This vaccine contains cow fetus serum, chick embryo proteins, DNA and protein fragments from human fetal cells, and Glutamate.

Varicella (Chickenpox): Chickenpox is not common, is treatable, and severe complications occur in less than 1% of cases. In my child’s first 12 years of life, their chance of having a severe case is 1 in 25,000. Adverse reactions to this vaccine include: chickenpox-like rash, pneomonitis (severe lung inflammation that can require intensive care), bleeding problems, neurological reactions, stroke, encephalitis, spinal cord inflammation and dysfunction, GBS, seizures, facial nerve paralysis, meningitis, pnemonia, Stevens-Johnson Syndrome, bacterial skin and tissue infections, and more. This vaccine contains Gelatin, which is against my religion to consume, as well as MSG, DNA and protein from human cells, cow fetus serum, and animal cells. This vaccine sheds the Chickenpox virus in the vaccinated for 6 weeks.

Hep A: Hepatitis A is harmless to young children and preventative measures can be taken if they are exposed. Severe cases are extremely rare, and virtually all cases happen in teens and young adults. The risk in these ages is about 1 in 25,000 in teen and adult years of life. Adverse reactions to the shot include: Hepatitis, seizures, bleeding problems, GBS, encephalitis, difficulties with walking and balance, multiple sclerosis, severe anaphylactic allergic reactions, jaundice, fainting, spinal cord inflammation, vasculitis, nerve dysfunction, rashes, and flu-like symptoms.

Influenza (Flu): While the flu may be common, it’s treatable and VERY rarely are there complications from severe cases. There is a wide debate and some evidence that this shot doesn’t even work for children under 2 and the rate of side effects is unusually high, so that alone makes this not worth the potential side effects to me. The nasal mist is a live virus, so those who receive this are contagious with the flu for 6 weeks and are likely have a mild case of the flu after receiving this. Adverse reactions to the flu shot include: tonsillitis, asthma, arthritis, limb paralysis, tremors, difficulty swallowing, febrile seizures, GBS, bleeding from low platelet count, severe allergic reactions, seizures, inflammation of the brain and spinal cord, encephalopathy, dysfunction of nerves in the face, eyes, or arm, fainting, inflammation of blood vessels, Stevens-Johnson syndrome, chest pain, rapid heart rate, eye infection and redness/swelling, and more. There are many different flu vaccinations, so the list of harmful chemicals varies between them and is quite long. These include formaldehyde, MSG, and Mercury or Thimerosal which is incredibly harmful and toxic and has been removed (almost completely) from all other vaccines because of this.
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I hope that people will understand that not all parents who choose not to vaccinate their children are quacks who based their decisions off of Google searches, illegitimate sources, biased information, opinions, or conspiracy theories. While there are some people like that, most of us are not. I urge you to seek out peer reviewed investigatice research and consider its source, funding, and the factors that solidify or vindicate it such as amount of test subjects, presence of control groups and size, or factors that were overlooked. This is important in any research, whether it supports or opposes vaccinations. I encourage you to make the decision whether or not to vaccinate each of your children individually and that you with the risks and benefits specific to your child.

Investigative journalist reveals global vaccine conspiracy orchestrated by the WHO

On February 26, 2014, a public hearing was held under the direction of the Ministry of Health, Labor and Welfare in Tokyo, Japan in response to reports of adverse effects following  Gardasil vaccinations. Dr. Sin Hang Lee, MD, the Director of Milford Molecular Diagnostics Laboratory, testified on the behalf of parents whose children had either died, or experienced serious neurological complications after being given the HPV shots. As a pathologist, his hypothesis was straightforward:

“… the HPV vaccination depends on the Gardasil adjuvant. On the left-hand side, the aluminum adjuvant waits for the release of human DNA as a result of inflammation and the cell death. And the human DNA would combine with the aluminum and stimulate the macrophage to enhance the immunogenicity of the vaccine reaction. However, in Gardasil because the HPV DNA was already present in the vaccine when they were injected in these girls, so the viral DNA combined with the aluminum injected to stimulate the microphages. And that is the mechanism I believe to cause cytokine storm and tumor necrosis release. And that would cause hypotension, tachycardia, and sudden death. And other neurological symptom is called acute disseminated encephalomyelitis.”

Read more at:

http://www.vaccines.news/2016-05-11-investigative-journalist-reveals-global-vaccine-conspiracy-orchestrated-by-the-who.html

Science troll and cancer surgeon David Gorski (ORAC) named in conspiracy allegations filed with the FBI; Health Ranger to deliver ‘bombshell’ findings in sworn testimony

Yesterday, I filed a detailed series of medical conspiracy allegations against Dr. David Gorski and the Karmanos Cancer Center, where criminal cancer fraudster Dr. Farid Fata committed large-scale criminal fraud and was ultimately sentenced to 45 years in prison by the federal government.

You can read the allegations against David Gorski at this link.

Now I have also filed the same complaint with the Federal Bureau of Investigation, including additional notes affirming the willingness of myself and Natural News editorial staff to testify under oath to findings we have uncovered about Dr. David Gorski and the Karmanos Cancer Center.

Dr. David Gorski is a mentally ill science troll and cancer surgeon who is widely characterized as being psychologically unfit to practice medicine at all. He hid his real identity from the world for many years, blogging extreme hatred under the pseudonym “ORAC” until his real identity was finally uncovered. As ORAC, Dr. Gorski routinely engaged in deliberate deceptions, organized defamations, online scientific fraud and racketeering operations to discredit reasonable skeptics of vaccines, chemotherapy and conventional medicine. His pathological hatred and “internet terrorism” style of bullying and muckraking made him notorious for being the loudest source of hate speech and intimidation ever carried out in the name of “science” and “medicine.”

Astonishingly, no other physicians or even administrators at the Karmanos Cancer Center stopped his behavior. As I allege in my complaint filed with the FBI, Karmanos actively took part in tolerating or even advocating his activities, allowing him to carry them out from Karmanos property when he was supposed to be treating cancer patients.

Bombshell findings to be put on the record during sworn testimony

After months of investigations, during which I was personally targeted in an ongoing stream of malicious, defamatory and false attacks organized by Gorski, I am now sitting on what I consider to be “bombshell” findings that I am ready to hand over to law enforcement under oath. These findings, I believe, will provide law enforcement the information they need to indict Dr. David Gorski under multiple violations of both state and federal law, if they choose to do so.

Filing these allegations is not a decision I made lightly. Ultimately, witnessing the number of people who were maimed or murdered by Dr. Gorski’s colleague Dr. Farid Fata alerted me to the journalistic responsibility I hold to protect the interests of the people of Detroit, Michigan… mostly African-American people who have been systematically victimized and exploited by the corrupt, criminally-run cancer industry of Detroit. As a science lab director (CWClabs.com) and nutrition investigator (FoodForensics.com), I have long been aware of the cancer industry’s predatory practices when it comes to black people in America. Because of vitamin D deficiencies caused by darker skin pigmentation, black patients tend to have far more serious cancers than white patients. In the eyes of the for-profit cancer industry, this translates into more treatment profits by targeting blacks.

When we contacted Karmanos Cancer Center to ask for aggregate patient records that would help us determine the fatalities and racial makeup of Dr. Farid Fata’s victims, we were stonewalled by Karmanos staffers who were obviously covering up something quite serious. Although we don’t have patient records for this reason, my informed estimate is that perhaps 70% – 80% of Karmanos cancer patients in the Detroit area are African-American. That so many innocent people were ordered by Dr. Fata to undergo medically unnecessary (and extremely toxic) chemotherapy so that his business could reap a financial windfall from the pain and suffering of Detroit citizens is seemingly beyond comprehension… yet it literally happened. And it all took place under the same banner of “science” and “medicine” that David Gorski insists can do no wrong.

In fact, criminal fraud was the accepted revenue model of an entire business unit operating inside Karmanos. If not for a single employee finally blowing the whistle and going to the FBI with details of the large-scale criminal activity being carried out at the Karmanos Cancer Center, Dr. Fata would still be poisoning patients for profit this very day.

Importantly, the medical system did not correct itself. The institution of cancer kept profiting from the pain and suffering of Detroit citizens, and it was not until law enforcement got involved that the horrific “medical” practices of Dr. Fata were finally halted. No one stopped Dr. Fata, in other words, until handcuffs were finally slapped on him and he was removed from the hospital by force.

Read more at:

http://www.naturalnews.com/053751_David_Gorski_conspiracy_allegations_FBI_complaint.html