Vaccine News – Douglas Mackenzie MD says physicians are ignorant about vaccines #vaxxed #PrayBig #RFKcommission

Statement of William W. Thompson, Ph.D., Regarding the 2004 Article Examining the Possibility of a Relationship Between MMR Vaccine and Autism
My name is William Thompson.  I am a Senior Scientist with the Centers for Disease Control and
Prevention, where I have worked since 1998.
I regret that my coauthors and I omitted statistically significant information  in our 2004 article published in the journal Pediatrics. The omitted data suggested that African American males who received the MMR vaccine before age 36 months were at increased  risk for autism. Decisions were made regarding which findings to report after the data were collected, and I believe that the final study protocol was not followed.
I want to be absolutely clear that I believe vaccines have saved and continue  to save countless lives.  I would never suggest that any parent avoid vaccinating children of any race. Vaccines prevent serious diseases, and the risks associated  with their administration are vastly outweighed  by their individual and societal benefits.
My concern has been the decision to omit relevant findings in a particular study for a particular sub­ group for a particular  vaccine. There have always been recognized risks for vaccination and I believe it is the responsibility of the CDC to properly  convey the risks associated  with receipt of those vaccines.
I have had many discussions  with Dr. Brian Hooker over the last 10 months regarding studies  the CDC has carried out regarding vaccines and neurodevelopmental outcomes including autism spectrum disorders. I share his beliefthat CDC decision-making and analyses should be transparent. I was not, however, aware that he was recording any of our conversations, nor was I given any choice regarding whether  my name would be made public or my voice would be put on the Internet.

Vaccine injury testimony – Vaccines killed my 6 year old son. #vaxxed #VaccinesKill #PrayBig
If you feel it in your heart to donate to the Ramirez family please do so at Daniel Ramirez-Porter Jusice Support http://www.gofundme.com/32guy1s

Yale Study SHOWS Vaccines Cause Brain Disorders – RFK Jr.
By Paul Webber – February 11, 2017
Robert F. Kennedy Jr. has wasted little time as the newly appointed Vaccine Safety Czar of the Trump Administration. Kennedy has long championed the rights of those suffering from vaccine injury and now thanks to President Trump bringing the cause to mainstream, Kennedy has a powerful stage to generate discussion.
Now on the heels of a research study from Yale University, Kennedy has released the story on EcoWatch, Kennedy is on the board of the website.

Study – Temporal Association of Certain Neuropsychiatric Disorders Following Vaccination of Children and Adolescents: A Pilot Case–Control Study
Background: Although the association of the measles, mumps, and rubella vaccine with autism spectrum disorder has been convincingly disproven, the onset of certain brain-related autoimmune and inflammatory disorders has been found to be temporally associated with the antecedent administration of various vaccines. This study examines whether antecedent vaccinations are associated with increased incidence of obsessive–compulsive disorder (OCD), anorexia nervosa (AN), anxiety disorder, chronic tic disorder, attention deficit hyperactivity disorder, major depressive disorder, and bipolar disorder in a national sample of privately insured children.
Methods: Using claims data, we compared the prior year’s occurrence of vaccinations in children and adolescents aged 6–15 years with the above neuropsychiatric disorders that were newly diagnosed between January 2002 and December 2007, as well as two control conditions, broken bones and open wounds. Subjects were matched with controls according to age, gender, geographical area, and seasonality. Conditional logistic regression models were used to determine the association of prior vaccinations with each condition.
Results: Subjects with newly diagnosed AN were more likely than controls to have had any vaccination in the previous 3 months [hazard ratio (HR) 1.80, 95% confidence interval 1.21–2.68]. Influenza vaccinations during the prior 3, 6, and 12 months were also associated with incident diagnoses of AN, OCD, and an anxiety disorder. Several other associations were also significant with HRs greater than 1.40 (hepatitis A with OCD and AN; hepatitis B with AN; and meningitis with AN and chronic tic disorder).
Conclusion: This pilot epidemiologic analysis implies that the onset of some neuropsychiatric disorders may be temporally related to prior vaccinations in a subset of individuals. These findings warrant further investigation, but do not prove a causal role of antecedent infections or vaccinations in the pathoetiology of these conditions. Given the modest magnitude of these findings in contrast to the clear public health benefits of the timely administration of vaccines in preventing mortality and morbidity in childhood infectious diseases, we encourage families to maintain vaccination schedules according to CDC guidelines.

Flu Shot Causes Over 5x Times More Respiratory Infections – A Vaccinated vs. Unvaccinated Study
While the government in the U.S. continues to resist doing a true study on vaccinated vs. unvaccinated children or adults, stating that such a study would be “unethical”, researchers in Hong Kong have conducted a true vaccinated vs. unvaccinated study on the influenza vaccine. This is probably one of the few, if not only, true study conducted in recent times where a real placebo was actually used and compared to the vaccine. The results are quite remarkable, suggesting that it is unethical NOT to pursue more studies comparing vaccinated and unvaccinated populations. People receiving the flu vaccine suffered from other respiratory infections at a rate 5.5 times more than the placebo group!
Thanks to Heidi Stevenson at Gaia Health for providing her excellent analysis of this study in response to my request.
Vaccine Vials, by Sanofi Pasteur, Vaccine Profiteer
The utter absurdity of vaccination ‘science’ is revealed in this study. It claims a flu vaccine results in less disease risk because it causes antibodies to develop, in spite of not reducing the likelihood of contracting the disease and also resulting in 5.5 times more incidents of similar diseases!
by Heidi Stevenson Gaia Health
Would you be interested in a vaccination that results in more than 5 times as much illness? If you take the seasonal influenza vaccination, that’s what you’re doing. The seasonal trivalent flu vaccine results in 5.5 times more incidents of respiratory illness, according to a study published in Clinical Infectious Diseases.
The study is particularly noteworthy because it was a double-blind placebo-controlled trial—and the researchers used saline solution, a genuinely inactive placebo, as a standin for the trivalent flu vaccine. Most vaccine trials utilize active placebos, which are substances that include ingredients used in the vaccines, making the studies meaningless—though this fact is almost never revealed in the writeups.
Subjects were followed for an average of 272 days. The active influenza vaccine adminstered was Sanofi Pasteur’s Vaxigrip. The trial included children aged 6-15 years. 69 were given Vaxgrip and 46 received the saline placebo.
With regard to effectiveness against influenza, the authors wrote:
There was no statistically significant difference in the risk of confirmed seasonal influenza infection between recipients of TIV [trivalent influenza inactivated vaccine] or placebo.
The flu vaccine provided no benefit!
The authors tried to cover that by adding:
TIV recipients had significantly lower risk of seasonal influenza infection based on serologic evidence.
In other words, the authors are trying to suggest that, in spite of the fact that vaccine recipients suffered as much genuine influenza as those who’d received a placebo, they still benefited because of “serologic evidence”. This “serologic evidence” consists of antibodies produced as a result of the vaccine, which is the standard method of determining a vaccine’s effectiveness.
In other words, a vaccine’s effectiveness is not determined by whether it prevents disease, but rather by whether it causes antibodies to be produced!

Vaccine injury testimony – i’m a registered nurse and I know vaccines cause autism #vaxxed #praybig #RFKcommission

The 2017 Conscious Life Expo is coming soon. Check out the Vaccine Panel from last year. Camera and editing by Joshua Coleman
THE VACCINE PANEL: The Insider’s Report

This is the Vaccine Panel that was held on February 20, 2016 in Los Angeles at the Conscious Life Expo. The panel is moderated by Kelly Gallagher and the speakers include Dr. Andrew Wakefield M.D., Dr. Toni Bark, Karen Kain, Brandy Vaughan, Allison Jones, Wendy Silvers, Larry Cook and Dr. Nick Delgado. The discussion includes everything vaccine related including a Q&A from the audience. The panel was produced by Dawna Shuman B-roll camera by Jesus Curioso. Camera and editing by Joshua Coleman.

Human-Pig GMO Created at Vaccine Institute
February 07, 2017
By Dr. Mercola
In Greek mythology, a chimera is a fire-breathing monster created from different species, most often portrayed as a creature with a lion’s head, a goat’s body and a serpent’s tail.
Chimeras have long been regarded as mythical creatures, to the extent that the word “chimera” also means “an illusion or fabrication of the mind” or “an unrealizable dream.”1 Among humans, chimeras, or people who have two genetically distinct types of cells, do exist, however.
Most often this occurs among non-identical twins who shared a blood supply in the uterus and end up having more than one blood type (they’re known as blood chimeras). The idea of a human-animal chimera has remained confined largely to mythology, however — until now.
First Human-Pig Hybrid Created
Researchers from the Salk Institute for Biological Studies in La Jolla, California, have made history by creating a human-pig hybrid, a task achieved by injecting days-old pig embryos with human pluripotent stem cells.2 Such cells, like embryonic stem cells, are able to divide indefinitely and become any type of cell in the body.
The human-pig embryos were then transferred into adult pigs and allowed to grow for up to four weeks, before they were “removed and analyzed.”3
The study noted that more than 2,000 hybrid embryos were transferred into surrogate sows, but only 186 later-stage chimeric embryos survived the process, each with about 1 in 100,000 human cells.
The long-term goal of such research is to figure out if it’s possible to grow human organs inside other species, like pigs. Human embryo development, drug development and disease processes could also be studied using chimeras.
Animal chimeras have been developed in the past. For instance, researchers genetically engineered (GE) rat embryos to not produce a pancreas (which controls blood sugar levels), then injected mouse stem cells into them, which resulted in the growth of pancreatic tissue.
They were then able to treat diabetes by transplanting parts of the healthy organs into diseased mice.4
The development of human-animal chimeras has, however, remained in the realm of science fiction until now. Aside from the glaring ethical considerations, these types of experiments have been ineligible for public funding in the U.S., which is why the Salk Institute has had to rely on private funding for the study.5

India Boots Gates Foundation Citing Pharmaceutical “Conflict of Interest”
In 2009, tribal children (girls) of the Khammam district in Andhra Pradesh, India were given “well being” shots consisting of the HPV vaccine manufactured by Merck. In Vadodara, Gujarat, another 14,000 plus more tribal children used as guinea pigs. This time the “well being” shots were the HPV vaccine called Cervarix made by GlaxoSmithKline. Both vaccine “campaigns” had purposely denied the girls and their parents informed consent. Both “campaigns” were really official expanded trials of Merck and GlaxoSmithKline’s newly approved HPV vaccines. Both trials were in collaboration, directed, and implemented by the openly candid eugenics Gates Foundation. And both India HPV vaccine trials saw the health of a critical mass of the girls who received the unsafe vaccine rapidly deteriorate including some deaths.
In April 2010, the government of India called a halt to trials of the HPV vaccine. This came about because of a civil society-led investigation highlighted serious ethical violations in the trials. According to Economic and Political Weekly, the investigation that led to the ban highlights how:
“…the promotional practices of drug companies, pressure from powerful international organizations, and the co-option of, and uncritical endorsement by India’s medical associations are influencing the country’s public health priorities.”
Whistleblowers from the Indian NGO woman’s health group named Sama revealed how the young girls were being used as guinea pigs for vaccine trials all under the guise of receiving healthcare. Sama reported that those receiving the vaccine were given no informed consent while authorities made the people submit their thumb prints.
The recent news reported by the Economic Times of India states:
“The Centre has shut the gate on the Bill and Melinda Gates Foundation on a critical national health mission, and possible conflict of interest issues arising from the foundation’s “ties” with pharmaceutical companies is one of the reasons.
All financial ties of the country’s apex immunization advisory body, National Technical Advisory Group on Immunization (NTAGI), with the Gates Foundation have been cut off.”
Concerns from senior medical officials within India, arguments from members of the steering board of the National Health Mission, and the Swadeshi Jagaran Manch economic wing of the Hindu nationalist movement unified to blow the whistle on pharmaceutical “conflict of interest issues” within the NTAGI-Gates Foundation relationship. Gates and his foundation were given 20 days to wrap up their ties and exit their involvement with India’s Immunization Technical Support Unit at the Public Health Foundation of India. The official removal of the Gates Foundation from the affairs of India’s public health care comes after over a five year legal battle within India’s Supreme Court in which the foundation has been on trial for damage their vaccine programs have caused.
Coming into existence on November 22, 1991 People from all walks of life with distinct ideologies in India came together on the Swadeshi Jagaran Manch (SJM) platform to fight against “economic imperialism.” Playing a role in the recent removal the Gates Foundation from India, SJM’s national co-convener Ashwani Mahajan told the Economic Times of India, “We welcome this move by the government. We have always said foreign influence in our domestic policies in any way must be avoided.”

Ten Year Old Little Girl Paralyzed After Vaccination:
Nancy Grace had NO idea that Congress had removed the rights of Americans to sue for vaccine injury and death.
Due to this cruel, unjust reality, even though the legal system has ruled in favor of countless cases proving that the flu shot DOES cause ADEM (Acute Disseminated Encephalomyelitis), the vaccine injury that Marysue Grivna suffered, people like Amy Edwards can still go on TV and claim, “Gosh… we just don’t know if and how flu shots cause ADEM…..We think it is just a coincidence.”
An Update On Mary Sue’s Tragic Story: Now several years after suffering vaccine-induced paralysis, she is still bed-ridden, limited to speaking just ten words and must be carried from room to room by her father.

More on her story here – Fox News:

#RevolutionForChoice #VAXXED #InformedConsent

Unvaccinated and healthy #vaxxed #PrayBig

Dear Mr. President Why are 350 organizations trying to stop scientific research?
#Vaxxed #RFKCommission

Merck whistleblower Brandy Vaughan #vaxxed #PrayBig #RFKcommission

Vaccine injury story – Our Baby – Before and After Toxic Vaccinations:
#RevolutionForChoice #VAXXED #MMR

Douglas Mackenzie MD says physicians are ignorant about vaccines #vaxxed #PrayBig #RFKcommission

Yale University Study Shows Association Between Vaccines and Brain Disorders
Robert F. Kennedy, Jr.
A team of researchers from the Yale School of Medicine and Penn State College of Medicine have found a disturbing association between the timing of vaccines and the onset of certain brain disorders in a subset of children.
Analyzing five years’ worth of private health insurance data on children ages 6-15, these scientists found that young people vaccinated in the previous three to 12 months were significantly more likely to be diagnosed with certain neuropsychiatric disorders than their non-vaccinated counterparts.
This new study, which raises important questions about whether over-vaccination may be triggering immune and neurological damage in a subset of vulnerable children (something parents of children with autism have been saying for years), was published in the peer-reviewed journal Frontiers in Psychiatry, Jan. 19.
More than 95,000 children in the database that were analyzed had one of seven neuropsychiatric disorders: anorexia nervosa, anxiety disorder, attention deficit and hyperactivity disorder (ADHD), bipolar disorder, major depression, obsessive-compulsive disorder (OCD) and tic disorder.
Children with these disorders were compared to children without neuropsychiatric disorders, as well as to children with two other conditions that could not possibly be related to vaccination: open wounds and broken bones.
This was a well-designed, tightly controlled study. Control subjects without brain disorders were matched with the subjects by age, geographic location and gender.
As expected, broken bones and open wounds showed no significant association with vaccinations.
New cases of major depression, bipolar disorder or ADHD also showed no significant association with vaccinations.
However, children who had been vaccinated were 80 percent more likely to be diagnosed with anorexia and 25 percent more likely to be diagnosed with OCD than their non-vaccinated counterparts. Vaccinated children were also more likely to be diagnosed with an anxiety disorder and with tics compared to the controls.
In a carefully worded conclusion, the researchers caution making too much of these results while also urging further investigation. “This pilot epidemiologic analysis implies that the onset of some neuropsychiatric disorders may be temporally related to prior vaccinations in a subset of individuals,” they write. “These findings warrant further investigation, but do not prove a causal role of antecedent infections or vaccinations in the pathoetiology of these conditions.”

Study – Temporal Association of Certain Neuropsychiatric Disorders Following Vaccination of Children and Adolescents: A Pilot Case–Control Study
Results: Subjects with newly diagnosed AN were more likely than controls to have had any vaccination in the previous 3 months [hazard ratio (HR) 1.80, 95% confidence interval 1.21–2.68]. Influenza vaccinations during the prior 3, 6, and 12 months were also associated with incident diagnoses of AN, OCD, and an anxiety disorder. Several other associations were also significant with HRs greater than 1.40 (hepatitis A with OCD and AN; hepatitis B with AN; and meningitis with AN and chronic tic disorder).
Conclusion: This pilot epidemiologic analysis implies that the onset of some neuropsychiatric disorders may be temporally related to prior vaccinations in a subset of individuals. These findings warrant further investigation, but do not prove a causal role of antecedent infections or vaccinations in the pathoetiology of these conditions. Given the modest magnitude of these findings in contrast to the clear public health benefits of the timely administration of vaccines in preventing mortality and morbidity in childhood infectious diseases, we encourage families to maintain vaccination schedules according to CDC guidelines.

Dr. Patricia Ryan randomly comes across the VaxXed Team when they were in Nebraska and does an impromptu interview with Polly Tommey. Her truth brings Polly to tears.
Camera and editing by Joshua Coleman

Dr. Andrew Wakefield Interview, How to End the Autism Epidemic
Dr. Andrew Wakefield, a British doctor, may understand the issue of vaccine-induced autism better than anyone on the planet. Listen to the doctor-turned filmmaker (Vaxxed) tell the truth about how to end the autism epidemic.

Flu Shot Ingredients & Why You Should NEVER Get One
Flu shot hysteria is in full swing. In some ways, the most dangerous flu shot ingredients are the socio-political elements that make up the hysteria: drug company marketing, co-worker bullies, corporate mandates. I can’t tell you how many stories I hear from readers who are bullied and subjected to discrimination at corporate offices. It is utterly appalling.
But there are actual ingredients which are, well, pretty bad. They are disgusting. Here are a few:
Formaldehyde: You know, the stuff your science class preserved frogs in. This stuff is also used to maintain (stabilize) your flu vaccine concoction. Formaldehyde is a colorless and flammable substance often used in household cleaning products. You can, as alluded to before, embalm a dead body using it. It has been linked to neurological damage and metabolic acidosis. It can make it difficult for you to breath and possible kidney failure. It has also been classified as a carcinogen for humans, which means it causes cancer.
Aluminum: This is used as an “adjuvant.” The goal is to stimulate an immune response. Aluminum, however, is a neurotoxin. It has been linked to Alzheimer’s, Parkinson’s and dementia. Some studies on humans have even shown it to cause nerve death.
Phenol: This is supposed to help stimulate an immune response. It was used by Nazis to exterminate Jews during WW2. It is also used in weed killers to help kill weeds. Reproductive systems, liver, kidneys and even the skin suffer serious side effects with Phenol.
This is only a few of the real ingredients. Why on earth would anyone take this shot?
Just how well does the flu shot work?
This graph is taken from the CDC website. The shot in 2014-2015 flu season protected people at a 23% rate?

Seasonal Influenza Vaccine Effectiveness, 2005-2016
CDC conducts studies to measure the benefits of seasonal flu vaccination each flu season to help determine how well flu vaccines are working. These vaccine effectiveness (VE) studies regularly assess and confirm the value of flu vaccination as a public health intervention. Study results of vaccine effectiveness can vary based on study design, outcome(s) measured, population studied and the season in which the flu vaccine was studied.
CDC has been working with researchers at universities and hospitals since the 2003-2004 flu season to estimate how well flu vaccine works through observational studies using medically attended laboratory-confirmed flu as the outcome. This is the U.S. Flu Vaccine Effectiveness (VE) Network. The U.S. Flu VE Network currently consists of five study sites across the United States that measure the flu vaccine’s effectiveness at preventing outpatient medical visits due to laboratory-confirmed influenza. CDC’s observational studies at U.S. Flu VE Network sites measure outpatient visits* for laboratory-confirmed influenza infections using a highly accurate lab test called rRT-PCR to verify the outcome. These studies compare the odds of vaccination among outpatients with acute respiratory illness and laboratory-confirmed influenza infection to the odds of vaccination among outpatients with acute respiratory illness who test negative for influenza infection.
The overall, adjusted vaccine effectiveness estimates for influenza seasons from 2005-2016 are noted in the chart below. (Estimates are typically adjusted for study site, age, sex, underlying medical conditions, and days from illness onset to enrollment.)

You asked for the uncut version of the Paul Offit incident and here it is. Enjoy!! #VaxXed #PaulOffit #VaxWithUs
Camera by Joshua Coleman and Polly Tommey with editing by Joshua Coleman

Joshua Coleman sees Paul Offit eating breakfast in New York on November 21, 2016 and approaches him for a polite conversation. Paul wasn’t up for it. This shows both TEAMVAXXED’s Periscope footage and Joshua Coleman’s HD footage split screen and UNCUT! Camera and editing by Joshua Coleman.

Vaccine-Induced SSPE Observed After MMR Vaccinations
Measles Vaccine Scandal: World Governments Have Known It Can Cause Neurological Disorders Since 1970’s
A staggering 15 years later, during the ARVI (Adverse Reaction to Vaccination and Immunization) meeting 6th July 1987, Section 4 – Item 5 – MMR vaccine – 5.4 Postpartum Rubella immunisation associated with development of prolonged arthritis neurological sequelae and chronic rubella arthritis Tingle et al. J. of Inf. Diseases (1985), Vol 152: pages 606-612 the committee members can be seen discussing points raised in the previous ARVI meeting. [5]

Subacute Sclerosing Panencephalitis (SSPE) – Facts and Information
Defining SSPE:
SSPE is a form of progressive neurological disorder that affects the central nervous system of children and young adults. The disorder is slow yet persistent, and is a viral infection caused by defective measles virus. SSPE is found in every part of the world today, but is considered to be a rare disease in developed nations with less than ten-percent of people who experience the disorder in America. Widespread immunization with measles vaccine has found a ninety-percent decline in the incidence of SSPE in nations that practice such immunization. In the nations of India and Eastern Europe the incidence of SSPE remains high. There is also a higher incidence rate among males than females with a ratio of three to one.
Many young people with SSPE present a history of measles infection at an early age, commonly before the age of two, followed by a latent period of six to eight years prior to the onset of neurological symptoms. Researchers believe that despite the long interval between the initial measles infection and the onset of SSPE, the infection of the person’s brain happens soon after the primary measles infection, and then progresses at a slow rate. The reasons behind the persistence and slow progression of the disorder remain unknown.
The symptoms a person with SSPE experiences are subtle. They usually include symptoms such as changes in behavior and mild mental deterioration such as memory loss. The symptoms that follow are commonly involuntary jerking movements of the person’s head, limb or trunk jerks, and additional motor function disturbances. The person may experience seizure activity, or become blind. As the disorder advances, the affected person might lose the ability to walk as their muscles spasm or stiffen. The person progresses towards a comatose state, followed by a vegetative state. People with SSPE commonly die as a result of fever, heart failure, or their brain’s inability to continue controlling their autonomic nervous system.
Encephalitis as a whole involves a rare complication of measles infection and is categorized into three unique types. The types of encephalitis include acute encephalitis, subacute sclerosing encephalitis (SSPE), as well as subacute measles encephalitis in the immuno-suppressed. Acute encephalitis is most likely a form of autoimmune phenomenon and not an infection of the person’s brain tissue. SSPE involves a progressive course that commonly begins a number of years after the person experiences an acute infection with the measles virus during their early childhood. A defective measles virus, or vaccination, may also lead to the progression of SSPE. The disorder itself is clinically characterized by a slow and erratic course that many times results in the death of the person affected. SSPE is also referred to by the names, ‘Subacute sclerosing leukoencephalitis,’ and, ‘Dawson’s encephalitis.’
Symptoms of SSPE:
The list of signs and symptoms associated with Subacute Sclerosing Panencephalitis (SSPE) is long. The symptoms of SSPE can include the following:

    Coma
Death
Seizures
Irritability
Dementia
Blindness
Spasticity
Memory loss
Optic atrophy
Hyperthermia
Unsteady gait
Abnormal EEG
Myoclonic jerks
Cortical blindness
Brain inflammation
Behavioral changes
Very tense muscles
Progressive dementia
Involuntary movements
Intellectual deterioration
Homeostasis disturbances
Neurological deterioration
Increased measles antibodies in blood
Increased measles antibodies in cerebrospinal fluid
Increased gammaglobulin levels in cerebrospinal fluid

Causes of SSPE:
The measles virus usually does not cause brain damage. An abnormal immune response to the measles, or a potential mutant form of the virus, can cause either severe illness or death. Such a reaction can lead to inflammation of the person’s brain, to include swelling and irritation of the person’s brain that can last for a number of years. SSPE is a disorder that has been reported in all parts of the world, although in western nations it is considered to be a rare form of disease. In nations such as India, greater than twenty persons per million are affected by SSPE each year.

Get to know Dr. Suzanne Humphries and Forrest Maready!
In part 1 of this 4 part interview, Forrest and Dr. Suzanne give a brief summary of their background and how they became involved in the subject of vaccines.
Watch Forrest Maready’s My Incredible Opinion series: https://www.youtube.com/channel/UCwc0nUV55sTXXwS2E8UchmA
Learn more about Dr. Suzanne Humphries, her books and watch her infomative videos:http://drsuzanne.net/
#RFKcommission #VaxXed

Scientist Attacked for Proving GMO Dangers Wins Defamation Suit in French Court

Scientist Attacked for Proving GMO Dangers Wins Defamation Suit in French Court
Remember Professor Giles-Eric Seralini and his research team at the University of Caan in France? They provided pictures of rats fed Monsanto GMO corn saturated with Roundup weed killer. That’s why the corn is genetically modified, to survive the most dangerous herbicide on the planet.
Their study discovered that rats fed GMOs developed tumors and died prematurely. But that wasn’t the purpose of their study. It was set up to examine the long term toxicity potential of eating Monsanto’s GMO corn along with the inherent exposure to Roundup.
Seralini and his research team weren’t completely satisfied with getting their studies republished and defending their work to a mostly uninterested mainstream media. They formed a group called CRIIGEN, the acronym for Comité de Recherche et d’Information Indépendantes sur le Génie Génétique, or Committee for Independent Research and Information on Genetic Engineering, and fought back.
Keep in mind the attacks on Seralini et al focused on the tumors, which had a high visual media impact. But Seralini and team weren’t testing for cancerous effects primarily. Their toxicity analysis focused on long term effects on liver and kidney health, where they did find indisputable evidence of gross harm.

Vaccines are useless against GMO bioweapons; boosting non-specific immune system is best defense, says former Soviet scientist

Dr. Kanatjan Alibekov was the former First Deputy Director of Biopreparat from 1988 to 1992. Biopreparat was the Soviet Union’s biological weapons program. Alibekov defected from the Soviet Union and moved to Washington, DC in 1992.

Read more at:
http://www.pbs.org/wgbh/pages/frontline/shows/plague/interviews/alibekov.html

Dr. Kanatjan Alibekov was the former First Deputy Director of Biopreparat from 1988 to 1992. Biopreparat was the Soviet Union’s biological weapons program. Alibekov defected from the Soviet Union and moved to Washington, DC in 1992.

Have we, at this point, put enough scientists, money and effort into trying to find a solution to this?

If we analyze the level of development of biological weapons, and the level of development of bio-defense, probably the gap is about 20-25 years. Now we are developing protection against the weapons developed 20-25 years ago. We have absolutely nothing against modern versions of biological weapons. If we continue this approach, we would never be able to catch up. What we need to do is stop for a second and think what is the best way. In my opinion, there is a way and I say this all the time: Vaccines are not a magic bullet. We wouldn’t be able to protect a population using vaccines, because they are capable to do this work in some cases, but this is not a comprehensive protection. If we do not understand that there are other ways, and we don’t start analyzing and researching these ways, we will never be able to develop a good protection. We need to start developing so-called immune boosting protective preparations. That’s the only way to make these weapons useless.

s one problem with the vaccines that there is always a variety of bugs that could be used?

First of all, the amount of agents [that] could be used in biological weapons averages 50-70. But if we add possible genetically altered agents, this figure reaches 100 and more. Could somebody imagine 100 vaccines? Could somebody imagine that groups or population vaccinated against dozens or even hundreds possible diseases? That’s impossible.

Why? What would happen to somebody who is vaccinated?

First of all, we don’t have such amount of vaccines. Second, if you vaccinate simultaneously against five, six, seven or ten diseases, this person could die just after such huge amount of vaccination. Of course, if you vaccinate against one or two diseases, that’s not a problem.

And another problem we need to discuss: What is possible for the troops, is absolutely impossible for civilian population. I cannot imagine how we can vaccinate the entire population of the United States against agents. And even if we had all these vaccines, it wouldn’t be possible to vaccinate because it’s impossible. We need to start thinking using some other ways.

In many cases, [there is] no necessity to develop vaccines. We [can’t] forget that our bodies have so-called non-specific immune system. If we are able to develop preparations to boost our non-specific immune system, it would be helpful to develop so-called pre-exposure, post-exposure preparations. It would be not to use for civilian population. If we’re talking about treatment when a set of symptoms appears, for example, after using biological weapons, we need to develop specific treatments based on so-called direct action drugs and then substances that could boost non-specific immune system as well.

So what’s the first thing that needs to be done?

In my opinion, we need to stop thinking that biological weapons are very terrifying and that we can’t find any protection. We can’t forget the ultimate objective … when we talk about bio-defense … to save peoples’ lives … we need to start developing medical defense, because medical defense is able to protect people against biological weapons. If we understand that not just vaccines are capable to protect people, because in many cases it’s impossible to vaccinate the entire population of the country against all possible agents. It’s absolutely impossible. But there are some approaches, and these approaches could be used for developing medical defense against biological weapons.

Do we need to bring experts together in Washington to analyze the situation, to figure out a direction? Where are we now?

Now, we are working mostly on developing vaccines. But what our government needs to do is gather the scientists who are knowledgeable in the area of bio-defense, … people who are knowledgeable in bio-offensive issues and we need to develop a national program of medical bio-defense. That’s the only way to make these weapons useless, maybe for a relatively short period of time, for three to five years.

Can you explain what is that defense? What do we need to do? Is it storehouse vaccines?
For now, vaccines [are] a temporary solution. But for the military, maybe it’s a good solution. But even for the military, I don’t believe it’s a comprehensive solution. We need to start thinking [about] using some different ways, because there is our own so-called protection system, immune system. If we are able to boost our immune system, non-specific immune system, that’s the most appropriate and the only way to develop protection. If we are able to develop special protective preparations, so-called pre-exposure, post-exposure preparations, treatment regimens based on boosting non-specific immune system, probably that’s the only way to develop comprehensive protection against BW.

Desperate medical monopolists warn not to call breastfeeding ‘natural’ because it might train women to avoid ‘unnatural’ medical interventions like vaccines or GMOs

Medical experts are taking up issue with use of the word natural when describing the behavior, saying that the word could make people leery of other health-related topics like GMOs and vaccinations, which already face their fair share of resistance and pressures by those who consider them “unnatural.”
Talk about a stretch. This has to be the most ridiculous over-analyzation of a word yet. Even worse is the fact that these experts are implying that the likes of vaccines and GMOs are natural, and that they actually think that calling breastfeeding “natural” will somehow interfere with the wonderful goodness that is getting a shot of mercury in your arm or eating health-destroying Frankenfoods.

Read more at:

http://www.naturalnews.com/053380_breastfeeding_natural_health_medical_monopolists.html

Republished study: long-term toxicity of a Roundup herbicide and a Roundup-tolerant genetically modified maize

Republished study: long-term toxicity of a Roundup herbicide and a Roundup-tolerant genetically modified maize

The health effects of a Roundup-tolerant NK603 genetically modified (GM) maize (from 11% in the diet), cultivated with or without Roundup application and Roundup alone (from 0.1 ppb of the full pesticide containing glyphosate and adjuvants) in drinking water, were evaluated for 2 years in rats. This study constitutes a follow-up investigation of a 90-day feeding study conducted by Monsanto in order to obtain commercial release of this GMO, employing the same rat strain and analyzing biochemical parameters on the same number of animals per group as our investigation. Our research represents the first chronic study on these substances, in which all observations including tumors are reported chronologically. Thus, it was not designed as a carcinogenicity study. We report the major findings with 34 organs observed and 56 parameters analyzed at 11 time points for most organs.

More at:

http://www.enveurope.com/content/26/1/14

or:

http://www.gmoseralini.org/republication-seralini-study-science-speaks/

Failed Monsanto GMO Corn Pushed on African Countries with Help of Bill Gates

Failed Monsanto GMO Corn Pushed on African Countries with Help of Bill Gates

Elizabeth Renter Infowars.com November 17, 2013

Even if you aren’t opposed to genetically modified crops (with all this information, how couldn’t you be) and even if you like Bill Gates and his ventures (but with all this information, how could you), this latest should be enough to get you perturbed. And if you are anti-GMO and knowledgeable of the shady and questionable ways of the Gates Foundation, this latest story out of Africa will truly make your blood boil.

 

According to a recent statement from the African Centre for Biosafety (ACB), failed GM corn from Monsanto is now being pushed on African countries with help from the Gates Foundation. This maize, known as MON810, has been grown in South Africa for 15 years, where it “failed miserably”. But so as not to call the seed a complete waste, Monsanto and Bill Gates are now pushing it into countries like Mozambique, Uganda, Tanzania, and Kenya—countries that need agricultural help.

Monsanto got the science completely wrong on this one. Independent biosafety scientists have discovered that the inheritance of resistance in African stem borers is a dominant, not recessive, trait as erroneously assumed,” explained the Director of the ACB Miriam Mayet. “Hence the insect resistance management strategies that Monsanto developed, and accepted by our regulators, based on these erroneous assumptions, were utterly ineffective.”

What this means, simply, is that pests in South Africa developed a massive resistance to the chemicals in the corn, annihilating the one prominent argument for GM crops, that it is resistant to insects. The corn was such a disaster that Monsanto willingly compensated farmers for the pesticides they had to spray on their crops to further fight the insects. Compensation from Monsanto? Weird.

Now, to not waste the waste of a seed, Monsanto has donated the MON810 technology to a “philanthropic” venture of the Gates Foundation and Monsanto called Water Efficient Maize for Africa (WEMA), and they’ve done it royalty-free.

Kaua’i city council slaps down Monsanto with unprecedented new restrictions on GMOs and toxic pesticides

Kaua’i city council slaps down Monsanto with unprecedented new restrictions on GMOs and toxic pesticides

NaturalNews) A milestone has just been achieved on the island in Kaua’i, where the city council passed measure 2491 which places unprecedented new restrictions on toxic agricultural chemicals frequently used in conjunction with GMOs.
Few people realize that Kaua’i is ground zero for chemical experimentation in agriculture. The island hosts 15,000 acres of crop lands which are experimentally exploited by biotech companies and chemical manufacturers. As a result, Hawaiians who live on Kaua’i are exposed to a toxic cocktail of synthetic chemicals on a routine basis.
The bill passed by a vote of 6 to 1, with councilman Mel Rapozo siding with the biotech industry and voting no. Hawaii Governor Abercrombie appears to be set against the bill and tried to block its passage. The biotech industry, as usual, has been busily engaged in false, defamatory, deceptive and even criminal actions in trying to block this city council measure. The industry, for example, routinely bribes scientists to publicly oppose bills restricting GMOs while falsely claiming they have no financial ties to the industry.

What 2491 establishes and requires

The protection provisions of 2491 require:
1) Buffer zones between chemical fields and schools, parks, beaches and hospitals.
2) Disclosure of GMO crops (until now, they have largely remained a secret).
3) Public notification before chemical spraying so that concerned citizens can leave the area and limit their exposure.
4) A county-level environmental assessment of the potentially hazardous effects of the toxic chemicals being sprayed on agricultural crops.
5) Full disclosure of the exact pesticides and herbicides being sprayed, as well as location details of where spraying is taking place.

Help support Hawaii’s continued victory against toxic agriculture

An email sent to me by key proponents of 2491 says:
Our massive campaigns across Hawai’i will continue over the next few months, we must pass Bill #113 on Hawai’i Island. On Oahu, after 18 months of pressure, it is time for Kamehameha Schools to EVICT MONSANTO from Hale’iwa. The largest lease to any GMO company on Oahu is the Kamehameha Schools lease of 1,033 acres above the most famous surf breaks in the world. No environmental assessment of chemical contamination has ever occurred in Hale’iwa. Any day, the chemical companies will file a lawsuit to block the implementation of 2491. The chemical companies are fighting for [their desire] to spray toxic chemicals, (many of them are banned throughout the world) less then 500 feet from schools, such as Waimea Canyon Middle School.

Where to learn more about GMO justice in Hawaii

Hawaii GMO Justice: http://www.facebook.com/HawaiiGMOJustice
Stop Poisoning Paradise: http://www.stoppoisoningparadise.org
Hawaii Seed: http://hawaiiseed.org
Kaua’i Rising: http://kauai-rising.org