blows

Feature BMJ Investigation

Revelations of poor practices at a contract research company helping to carry out Pfizer’s pivotal covid-19 vaccine trial raise questions about data integrity and regulatory oversight. Paul D Thacker reports

In autumn 2020 Pfizer’s chairman and chief executive, Albert Bourla, released an open letter to the billions of people around the world who were investing their hopes in a safe and effective covid-19 vaccine to end the pandemic. “As I’ve said before, we are operating at the speed of science,” Bourla wrote, explaining to the public when they could expect a Pfizer vaccine to be authorised in the United States.1

But, for researchers who were testing Pfizer’s vaccine at several sites in Texas during that autumn, speed may have come at the cost of data integrity and patient safety. A regional director who was employed at the research organisation Ventavia Research Group has told The BMJ that the company falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial. Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding. After repeatedly notifying Ventavia of these problems, the regional director, Brook Jackson, emailed a complaint to the US Food and Drug Administration (FDA). Ventavia fired her later the same day. Jackson has provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails.

Poor laboratory management

On its website Ventavia calls itself the largest privately owned clinical research company in Texas and lists many awards it has won for its contract work.2 But Jackson has told The BMJ that, during the two weeks she was employed at Ventavia in September 2020, she repeatedly informed her superiors of poor laboratory management, patient safety concerns, and data integrity issues. Jackson was a trained clinical trial auditor who previously held a director of operations position and came to Ventavia with more than 15 years’ experience in clinical research coordination and management. Exasperated that Ventavia was not dealing with the problems, Jackson documented several matters late one night, taking photos on her mobile phone. One photo, provided to The BMJ, showed needles discarded in a plastic biohazard bag instead of a sharps container box. Another showed vaccine packaging materials with trial participants’ identification numbers written on them left out in the open, potentially unblinding participants. Ventavia executives later questioned Jackson for taking the photos.

Early and inadvertent unblinding may have occurred on a far wider scale. According to the trial’s design, unblinded staff were responsible for preparing and administering the study drug (Pfizer’s vaccine or a placebo). This was to be done to preserve the blinding of trial participants and all other site staff, including the principal investigator. However, at Ventavia, Jackson told The BMJ that drug assignment confirmation printouts were being left in participants’ charts, accessible to blinded personnel. As a corrective action taken in September, two months into trial recruitment and with around 1000 participants already enrolled, quality assurance checklists were updated with instructions for staff to remove drug assignments from charts.

In a recording of a meeting in late September2020 between Jackson and two directors a Ventavia executive can be heard explaining that the company wasn’t able to quantify the types and number of errors they were finding when examining the trial paperwork for quality control. “In my mind, it’s something new every day,” a Ventavia executive says. “We know that it’s significant.”

Ventavia was not keeping up with data entry queries, shows an email sent by ICON, the contract research organisation with which Pfizer partnered on the trial. ICON reminded Ventavia in a September 2020 email: “The expectation for this study is that all queries are addressed within 24hrs.” ICON then highlighted over 100 outstanding queries older than three days in yellow. Examples included two individuals for which “Subject has reported with Severe symptoms/reactions … Per protocol, subjects experiencing Grade 3 local reactions should be contacted. Please confirm if an UNPLANNED CONTACT was made and update the corresponding form as appropriate.” According to the trial protocol a telephone contact should have occurred “to ascertain further details and determine whether a site visit is clinically indicated.”

Worries over FDA inspection

Documents show that problems had been going on for weeks. In a list of “action items” circulated among Ventavia leaders in early August 2020, shortly after the trial began and before Jackson’s hiring, a Ventavia executive identified three site staff members with whom to “Go over e-diary issue/falsifying data, etc.” One of them was “verbally counseled for changing data and not noting late entry,” a note indicates.

banned.video – Biggest Vaccine Whistleblower in History Exposes FDA Falsified Data in COVID Jab Trials, says Robert Barnes

https://banned.video/watch?id=6182de38c1526b2b32761399

Robert Barnes of https://vivabarneslaw.locals.com/ to break down the biggest vaccine whistleblower news in history as the FDA is exposed falsifying data in COVID jab trials.

More on the news here: https://www.infowars.com/posts/whistleblower-exposes-multiple-issues-with-pfizers-covid-vaccine-trial/

Leading medical journal The BMJ has published an incendiary report exposing faked data, blind trial failures, poorly trained vaccinators, and a slow follow-up on adverse reactions in the phase-three trial of Pfizer’s Covid jab.

Central to the exposé is Brook Jackson, who, for two weeks, served as regional director at Ventavia Research Group, the company contracted to assist with the pivotal trial. She provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails supporting her concerns.

Jackson reveals that Ventavia staff who conducted quality-control checks were overwhelmed by the volume of problems they were identifying. She repeatedly informed her superiors of poor laboratory management, and patient safety and data integrity issues.

In a cited internal document from August 2020, shortly after the Pfizer trial began, a Ventavia executive identified three site staff members with whom to “go over e-diary issue/falsifying data, etc.” One employee was said to have been subsequently “verbally counseled for changing data” and “not noting late entry.”

Jackson reported her concerns to the US Food and Drug Administration (FDA), but was fired later the same day on the basis that she was “not a good fit.”

In a recording of a late September meeting provided by Jackson, in which she met with two Ventavia directors, the unwelcome prospect of an FDA inspection had been openly discussed. “We’re going to get some kind of letter of information at least, when the FDA gets here … I know it,” one said to Jackson.

Another former Ventavia employee has confirmed that the company had been expecting a federal audit of its Pfizer vaccine trial, though this did not materialize. A 2007 US Department of Health report found that, between 2000 and 2005, the FDA inspected just 1% of clinical trial sites, while, in 2020, just 50 on-site visits were conducted.

In the aforementioned recording, an executive can also be heard explaining that, when examining paperwork for trial quality control, the company wasn’t able to quantify the types and number of errors that were being identified. “In my mind, it’s something new every day,” the senior staffer says. “We know that it’s significant.”

An email sent in September to Ventavia by Icon, the research organization with which Pfizer partnered on the trial, shows Icon was dissatisfied with Ventavia’s inability to keep up with data entry queries. Icon reminded Ventavia that “the expectation for this study is that all queries are addressed within 24 hours,” noting that more than 100 queries had remained outstanding for more than three days.

Among those queries were two cases in which test subjects had “reported with severe symptoms/reactions.” According to protocol, subjects experiencing grade-three local reactions – “severe” redness, swelling, or pain at the injection site – should have been contacted. Icon asked for confirmation as to whether contact had indeed been made, so as “to ascertain further details and determine whether a site visit is clinically indicated,” and that the subjects’ forms be updated accordingly.

And Here: https://www.bmj.com/content/375/bmj.n2635

The BMJ – Covid-19: Researcher blows the whistle on data integrity issues in Pfizer’s vaccine trial

Concerns raised

In her 25 September email to the FDA Jackson wrote that Ventavia had enrolled more than 1000 participants at three sites. The full trial (registered under NCT04368728) enrolled around 44 000 participants across 153 sites that included numerous commercial companies and academic centres. She then listed a dozen concerns she had witnessed, including:

Participants placed in a hallway after injection and not being monitored by clinical staff
Lack of timely follow-up of patients who experienced adverse events
Protocol deviations not being reported
Vaccines not being stored at proper temperatures
Mislabelled laboratory specimens, and
Targeting of Ventavia staff for reporting these types of problems.

Within hours Jackson received an email from the FDA thanking her for her concerns and notifying her that the FDA could not comment on any investigation that might result. A few days later Jackson received a call from an FDA inspector to discuss her report but was told that no further information could be provided. She heard nothing further in relation to her report.

In Pfizer’s briefing document submitted to an FDA advisory committee meeting held on 10 December 2020 to discuss Pfizer’s application for emergency use authorisation of its covid-19 vaccine, the company made no mention of problems at the Ventavia site. The next day the FDA issued the authorisation of the vaccine.8

In August this year, after the full approval of Pfizer’s vaccine, the FDA published a summary of its inspections of the company’s pivotal trial. Nine of the trial’s 153 sites were inspected. Ventavia’s sites were not listed among the nine, and no inspections of sites where adults were recruited took place in the eight months after the December 2020 emergency authorisation. The FDA’s inspection officer noted: “The data integrity and verification portion of the BIMO [bioresearch monitoring] inspections were limited because the study was ongoing, and the data required for verification and comparison were not yet available to the IND [investigational new drug].”

Other employees’ accounts

In recent months Jackson has reconnected with several former Ventavia employees who all left or were fired from the company. One of them was one of the officials who had taken part in the late September meeting. In a text message sent in June the former official apologised, saying that “everything that you complained about was spot on.”

Two former Ventavia employees spoke to The BMJ anonymously for fear of reprisal and loss of job prospects in the tightly knit research community. Both confirmed broad aspects of Jackson’s complaint. One said that she had worked on over four dozen clinical trials in her career, including many large trials, but had never experienced such a “helter skelter” work environment as with Ventavia on Pfizer’s trial.

“I’ve never had to do what they were asking me to do, ever,” she told The BMJ. “It just seemed like something a little different from normal—the things that were allowed and expected.”

She added that during her time at Ventavia the company expected a federal audit but that this never came.

After Jackson left the company problems persisted at Ventavia, this employee said. In several cases Ventavia lacked enough employees to swab all trial participants who reported covid-like symptoms, to test for infection. Laboratory confirmed symptomatic covid-19 was the trial’s primary endpoint, the employee noted. (An FDA review memorandum released in August this year states that across the full trial swabs were not taken from 477 people with suspected cases of symptomatic covid-19.)

“I don’t think it was good clean data,” the employee said of the data Ventavia generated for the Pfizer trial. “It’s a crazy mess.”

A second employee also described an environment at Ventavia unlike any she had experienced in her 20 years doing research. She told The BMJ that, shortly after Ventavia fired Jackson, Pfizer was notified of problems at Ventavia with the vaccine trial and that an audit took place.

Since Jackson reported problems with Ventavia to the FDA in September 2020, Pfizer has hired Ventavia as a research subcontractor on four other vaccine clinical trials (covid-19 vaccine in children and young adults, pregnant women, and a booster dose, as well an RSV vaccine trial; NCT04816643, NCT04754594, NCT04955626, NCT05035212). The advisory committee for the Centers for Disease Control and Prevention is set to discuss the covid-19 paediatric vaccine trial on 2 November.

Just News – Zerohedge – Female Kurdish Fighter Blows Herself Up As Turkish Tank Enters Syrian Village

Zerohedge – Female Kurdish Fighter Blows Herself Up As Turkish Tank Enters Syrian Village
A female fighter within the Kurdish People’s Protection Units paramilitary group has blown herself up amid an ongoing offensive by Turkey-led forces in Syria’s Afrin regional sources report. Sources following developments on the ground in Afrin are reporting that a Kurdish female fighter by the name of Avesta Khabur committed the suicide attack to in an attempt to turn back an armored assault by the Turkish Army.
Meanwhile, Turkish-backed Free Syrian Army (FSA) ground forces continue to advance on villages on the edges of Afrin Canton. Though Turkey claims it is “bringing peace” to the area, several FSA media accounts have released videos showing its Islamist fighters declaring their intent to conduct ethnic cleansing against the “atheist Kurds”.
Though a number of such videos with threats of genocide by invading Turkish and FSA forces have made the rounds over the last week, and though President Erdoğan himself in public speeches of late has used similar language, mainstream media in the West has continued to be mild or completely silent in its criticism of Erdoğan or the Turkish military invasion of Syria.
Indeed Erdoğan has recently vowed “to give Afrin back to its real owners” while claiming that “55% of Afrin is composed of Arabs with 35% of Kurds coming there later on”. Such language of militarily forced “demographic shift” inside another nation’s sovereign territory by Turkish leadership has gone relatively unreported in major international press.

Vaccine News – Everything You’ll Need to Know about Vaccines

Pet owner spreading vaccination awareness after senior pet’s death
By Alyssa Goard and Nadine Bonewitz Published: September 29, 2017,
AUSTIN (KXAN) — Joann Saathoff’s 14-year-old Pomeranian, Lexy, died on Sept. 24, and she believes the round of vaccinations Lexy received 12 days earlier led to her death.
Now Saatoff is trying to raise awareness about the options owners of senior pets have when it comes to getting shots for their furry friends.
It all started when Lexy went in for her annual check up. She was evaluated by the vet first, who said Lexy was in good health. Then Lexy received five shots, the same exact group of shots she’d received the year before. Within a few hours, Saathoff said her active dog had grown lethargic.
She took Lexy back to the vet the next day and they said her reaction was common, so they gave her an antibiotic and fluids. But Lexy’s condition continued to decline, the six pound dog threw up everything she ate. When she died, she weighed only three pounds. Saathoff said the cause of Lexy’s death was starvation, but the veterinarian told her that it started with the vaccinations which were “too much for her system.”
Saathooff began researching.
“I found out there’s a lot of senior dogs out there that can’t handle the full regimen of vaccinations,” she said.
She says she doesn’t blame her vet, she just wishes she knew about other options. Now she’s urging other pet owners to ask about what is best for their pets.
“My message to the community is you have options with your senior level dogs,” she said.

23 ‘must-see’ vaccine documentaries
By Britny Murray
In no particular order, here are 23 highly informative, must-see vaccine documentaries that you could share with your firends.
They all have to do with various factors of vaccination – evidence,, efficacy, injuries, health effects and medicinal politics.
They come with a brief description pulled from YouTube. Most of them are free and featured here in-full.

Deadly Immunity – Government Cover-Up Of A Mercury/Autism Scandal
Sep 30, 2017
World Mercury Project note: With the ongoing mainstream media blackout on questions regarding vaccine safety, we want to remind our followers of the publication–and subsequent retraction–of Robert F. Kennedy, Jr.’s 2005 article “Deadly Immunity” in Salon. The history of repression of crucial vaccine safety data runs deep. The article laid out the scientific link between thimerosal and childhood neurological disorders and published explosive excerpts from the transcripts from the CDC’s secretive June 2000 Simpsonwood conference which brought together government public health officials, vaccine manufacturers and professional medical associations. The article was groundbreaking at the time and received lots of media attention for uncovering the cozy relationship between government and industry at the expense of children’s health. Even though a dozen years have passed, the article’s facts have stood the test of time. An important read for people new to the movement and long-time advocates alike.

Transcript – Scientific Review of Vaccine Safety Datalink Information

Everything You’ll Need to Know about Vaccines
With this enormous effort in marketing vaccines and the money spent sponsoring large cohort studies showing that vaccines are always safe and effective, never expressing anything negative, and in some countries enforcing mandatory vaccine schedules wouldn’t any normal sensible person become a little suspicious and ask themselves..ARE THEY TRYING TO HIDE SOMETHING ??. It took the medical mafia 12 years to remove the evidence in Wakefield and Walker smith’s study analysis of 12 children with serious intestinal abnormalities that their parents confirmed had developed after receiving the MMR vaccine. The British media found a scapegoat using British journalist Brian Deer to uncover a potential conflict of interest to ‘blow the smoke away ‘ from the findings of the study. At the time autism was on the rise without explanation 6.2/10,000 births in 1990 to 42.5/10,000 births in 2001..for the most part the vaccine marketing machine ignored any correlation or causality toward their glorious vaccines. Why was Merck allowed to manufacture a Vaccine that included a benign children’s disease when the CDC confirmed there was no need to protect against Mumps, but the MMR vaccine was allowed anyway to be included in CDC’s vaccine schedule.

Appology to Polly Tommy
Gross misconduct from the Australian Government

Hammond vaccine terror #vaxxed #vaxxedperiscope

Donations to help our case and cause
Hi,
My name is Tanya and on the 26th of September 2012, James my son was born 8 weeks premature weighing in at just 2.4oz.
We live in a remote mining community in southern WA called Kalgoorlie and Ben, my beautiful husband, worked in the mines and because our son was born prem, he had to have a dTap vaccination and that’s just what you do. So just to be safe, as our entire family was protected and as good parents we believed we were, we always did the right thing.
James ended up and is doing fine but Ben, a healthy 34-year-old loving father and beautiful husband, sadly and totally unknowingly suffered the worst fate possible.
Both reported and recorded by the CDC (Centre for Disease Control) on their website, Ben had developed post vaccination ADEM (Acute Disseminated Encephalomyelitis) – our lives were shattered!
By October the 11th, 2012, Ben was classified a quadriplegic and since then, his health mentally, emotionally and physically has deteriorated so bad, that our lives will never be the same again.
Our vows in sickness and in health, no longer see any of the later and I’m now a full-time carer for Ben, no different than he would have done for me because our love for each other was so strong, but this curveball of life has put us to the test.
We’ve lost so much and are on the brink of extinction. We’re in surmounting debt, unable to work because we have 5 children and can’t afford childcare to work and bring home anything because the growing costs to care for Ben are not met with any government support.

Girl, 8, left with no skin after horrific allergic reaction to childhood vaccination meant it fell off when mum touched her
By Erin Elizabeth – September 26, 2017
At 18 months old, Isabel Olesen of Melbourne, Australia was taken to her pediatrician’s office for routine vaccinations (the kind that almost never cause a reaction and yet, our website is FULL of children who have suffered or died from very “rare” vaccine reactions) that ended up leaving her partially blind and covered with painful blisters all over her body, just 48 hours later.
Part of the problem with the one size fits all vaccine schedule is that you can’t tell when a child has Stevens-Johnson Syndrome (SJS) – a rare but life-threatening allergic reaction to medication or an infection. And Isabel had the worst form of SJS that doctors had ever seen. In fact, when Mom Edwina would touch her daughter, her skin would fall off. 1
It took three months of fighting for her life in the hospital, but even though Isabel lost the majority of her sight (SJS can break down the membranes around the eyes and cause them to become extremely dry) and needed to learn to walk, eat, and talk all over again- she’s now a healthy second grader who loves to ride her bike and run triathlons.

Real News with David Knight – EXPOSED: Secretive Vax Court
Wayne Rohde, author of “The Vaccine Court”, exposing the origins of the little known court that is the only recourse to those who have been harmed by vaccines. Wayne also explains what happened with the Somali population in Minnesota and why they refused vaccines.

TWO CHILDREN MURDERED VIA VACCINES IN KENYA!

Big Pharma Executive Blows Whistle on Vaccines: ‘Vaccinations are Deadly’ Pfizer Vice

President Dr. Peter Rost exposes dangers of Gardsil inoculation By: Jay Greenberg |@NeonNettle on 23rd September 2017
The former vice president of the world’s largest pharmaceutical company has blown the whistle to expose the true dangers of mandatory vaccinations. Dr. Peter Rost lifted the lid on vaccines and revealed that the Gardasil inoculation, in particular, is in fact, “deadly”. In a shocking exposé from one of the highest-ranking whistleblowers to date, Rost has also claimed that Big Pharma is purposely keeping the public unhealthy so they can make a fortune from continual treatments of illnesses rather than curing them. Dr. Rost made the revelations during an interview for the “One More Girl” documentary in which he candidly discussed how the main objective for vaccines and pharmaceutical drugs is to keep the public in a constant state of dis-ease. Rost also likened mandatory vaccinations to “child abuse” saying; “I would never vaccinate my children”

Vaccine News – “Vaccine injury is a long road. Don’t vaccinate and you won’t go down it!” – AreVaccinesSafe.org & “Vaccines, which I really love, can reduce sickness, reduce the population…” – Bill Gates

Pfizer Vice President blows the whistle: Reveals Dark Truth About Pharmaceutical Industry
Below is a clip taken from the “One More Girl” documentary, a film regarding the Gardasil vaccine, which was designed to prevent Human Papillomavirus. In it, Dr. Peter Rost, MD, a former vice president of one of the largest pharmaceutical companies in the world (Pfizer), shares the truth about the ties between the medical and pharmaceutical industry.
Rost is a former vice president of Pfizer, and a whistleblower of the entire pharmaceutical industry in general. He is the author of “The Whistleblower, Confessions of a Healthcare Hitman.” Considering his work experience, it would be an understatement to say that he is an insider expert on big pharma marketing.
Below are a couple of quotes from both a former and a current editor-in-chief of the two largest, and what are considered to be the most credible, medical journals in the world. It’s only fitting to include them into the article as they are directly related to what Dr. Rost hints at in the video.
“It is simply no longer possible to believe much of the clinical research that is published, or to rely on the judgment of trusted physicians or authoritative medical guidelines. I take no pleasure in this conclusion, which I reached slowly and reluctantly over my two decades as an editor of the New England Journal of Medicine.” – Dr. Marcia Angell, a physician and longtime editor-in-chief of the New England Medical Journal (NEMJ) (source)
“The case against science is straightforward: much of the scientific literature, perhaps half, may simply be untrue. Afflicted by studies with small sample sizes, tiny effects, invalid exploratory analyses, and flagrant conflicts of interest, together with an obsession for pursuing fashionable trends of dubious importance, science has taken a turn towards darkness.” – Dr. Richard Horton, the current editor-in-chief of the Lancet – considered to be one of the most well respected peer-reviewed medical journals in the world. (source)

Daily Mail – Teenager died in her sleep weeks after being given HPV vaccine as experts reveal the lives of thousands of girls have been destroyed by the controversial jab
Jasmin Soriat, 19, showed neurological symptoms after having a second HPV jab
The teen from Vienna suffered respiratory failure three weeks later
Pathologist said the vaccine could have been the cause of her death
British teenager Ruby Shallom is also included in the documentary, her family say she was left paralysed just days after having the jab
The stories of both girls are included in a new documentary in which doctors claim the HPV virus does not even cause cancer
By Claudia Tanner and Jacqui Deevoy For Mailonline
Published: 15:19, 27 September 2017

“Vaccines, which I really love, can reduce sickness, reduce the population…” What are your thoughts? Could Bill Gates actually be proposing we heavily vaccinate as a method to reduce world population?

Flu vaccine confers10 times the risk of developing alzheimer’s disease
Dr High Fudenberg claimed 10 times the risk of developing Alzheimer’s disease in those over 55 years old who received the flu vaccine 5 years in a row. According to Dr. Fudenberg, one of the world’s most prolific immunologists and 13th most quoted biologist of our times (over 600 papers in peer review journals), he had this to say regarding the annual flu vaccine program:
“If an individual has had 5 consecutive flu shots between 1970 – 1980 (the years of the study) his / her chance of developing Alzheimer’s Disease is 10 times greater than if they had one, two or no shots.” When asked why this is, Dr. Fudenberg stated that, “It is due to the mercury and aluminum buildup that is in every flu shot. The gradual mercury and aluminum buildup in the brain causes cognitive dysfunction.”
Hugh Fudenberg, MD, is Founder and Director of Research, Neuro lmmuno Therapeutic Research Foundation. Information from Dr. Hugh Fudenberg came from transcribed notes of Dr. Fudenberg’s speech at the NVIC International Vaccine Conference, Arlington, VA September, 1997. He trained from 1954–56 under William Dameshek former editor of Blood and completed a residency at Peter Bent Brigham Hospital from 1956–58. Fudenberg was formerly a Professor (first associate, and later full) of medicine at University of California, San Francisco (UCSF), as well as associate professor of immunology at the University of California, Berkeley. He was editor of the journal Clinical Immunology and Immunopathology for 15 years and developed the Rosette test as well. Additionally, Fudenberg sat on the World Health Organization’s expert committee on immunology for 20 years. In 1974, he relocated to South Carolina, specifically the Medical University of South Carolina, where he remained as a Professor until 1989

Big Pharma Is Injecting Us With Cancer Enzymes — Doctors Who Made the Discovery Found Murdered
Not long ago, Neon Nettle reported on the epidemic of doctors being murdered, most of which were in Florida, U.S.
The scientists all shared a common trait, they had all discovered that nagalase enzyme protein was being added to vaccines which were then administrated to humans.
Nagalese is what prevents vitamin D from being produced in the body, which is the body’s main defense to naturally kill cancer cells.
Nagalase is a protein that’s also created by all cancer cells. This protein is also found in very high concentrations in autistic children. And they’re PUTTING it in our vaccines!
Nagalese Cancer Vaccines
This prevents the body from utilizing the Vitamin D necessary to fight cancer and prevent autism. Nagalese disables the immune system. It’s also known to cause Type 2 Diabetes.
So basically… they weren’t killing these doctors because they had found the cure to cancer or were successfully treating autism… they’re killing them because these Dr’s had been researching and had the evidence that the vaccines they’re injecting our precious children with are CAUSING our current cancer and autism crisis!
And that it’s obviously being done knowingly and on purpose! The Dr’s they killed in FL had been collaborating and were getting ready to go public with the information.

2 More Alternative Doctors Go Missing After 3rd Found Dead In 2 Weeks
Dead doctors were ones who linked vaccines to autism

Vaccine injury is a long road. Don’t vaccinate and you won’t go down it!
AreVaccinesSafe.org

The Health Ranger – Interview with Dr Suzanne Humphries about vaccines
In this interview, you’ll hear Dr Humphries talk about vaccines, including: * Why she became concerned about vaccines after noticing kidney failure in patients who recently received vaccines. * Why vaccines are often contaminated with unknown viral strains, and why the vaccine industry has covered up known vaccine contamination (and knowingly sold contaminated vaccines to be used on the public). * Why the entire vaccine industry needs to be questioned, and why a new effort is needed to scientifically assess whether vaccines are really safe or effective. * Why the fairy tale that “vaccines eradicated polio” is a false mythology — here’s what really happened. * Why the “smallpox” vaccine has never been proven to be effective against smallpox at all. * Why vaccine industry research is extremely flimsy and ignores rigorous standards of scientific evidence. (Using improper placebos designed to minimize the appearance of side effects, for example.) * Why the vaccine industry won’t test vaccines versus unvaccinated children (they’re terrified of the results). * Why children caught up in outbreaks of measles are often the very same children who were vaccinated against measles! * Why vaccines may actually suppress the immune system and cause increased vulnerability to future infections. * Why many childhood infections such as chicken pox are perfectly natural, normal and even HEALTHY. * Why the outlandish and unscientific behavior of the vaccine industry is causing an erosion of credibility across all “science.”

La Chaine Qui Dérange – Isabelle Adjani à propos des 11 vaccins obligatoires

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