Vaccine Safety

H Res 1154 Conflates Vaccine Safety with Q Anon & Conspiracy Theories

Rep. Malinowski Official PhotoH Res 1154 is sponsored by Tom Malinowski (D) from New Jersey.

Vaccine safety, as important as any safety movement, has been lumped in with Q Anon.  Q ANON. It's a pretty big leap from blood drinking half humans, alien invasions and bomb threats to vaccine safety.  But wait. Maybe there is something else in play? Perhaps Q Anon has been used as a wrapping to shut down vaccine safety. Our Mothers taught us that we are known by the company we keep. Or the company we are said to keep? Either way, this legislation is a cruelty and an insult to every single American who has been harmed by a vaccine. Including so many of our own children. And probably a huge waste of effort while Americans struggle to stay afloat during Covid. But you can decide. (Thank you to reader MW for sending the link.)

Sponsor: Rep. Malinowski, Tom [D-NJ-7] (Introduced 09/25/2020)
Committees: House - Judiciary; Intelligence (Permanent Select)
Latest Action: House - 10/02/2020 Motion to reconsider laid on the table Agreed to without objection. (All Actions)

H. Res. 1154

In the House of Representatives, U. S.,

October 2, 2020.

Whereas, throughout history, conspiracy theories that falsely blame secret cabals or marginalized groups for society’s ills have fueled prejudice, genocide, and acts of terrorism;

Whereas QAnon is a movement promoting a collection of unfounded conspiracy theories that have spread widely on the internet since 2017;

Whereas QAnon initially alleged that prominent Americans are engaged in a secret plot to control the world, while using their power to exploit children, and has expanded to embrace virtually every popular conspiracy theory of the last several decades, from questioning the truth about the September 11th terrorist attacks, to believing in alien landings, to denying the safety of vaccines;

Whereas many QAnon followers express anti-Semitic views, and the Anti-Defamation League has said that the movement’s central conspiracy theory includes anti-Semitic elements;

Continue reading "H Res 1154 Conflates Vaccine Safety with Q Anon & Conspiracy Theories" »

36 Deaths Isn't Enough to Stop Flu Vax Program in S. Korea

Note: This is becoming almost a joke. Except people are dying, which is a tragedy. How many people must die before a vaccine program is halted? Meanwhile, how many people must be shunted into social isolation with devastating result while we (not us, that's the royal we...(Wait. it's not really royal, I don't think the Queen of England is holding her breath for a vaccine either) "We" wait for a vaccine like refugees on the Titanic waiting for lifeboats.  Spoiler alert - the lifeboats are made of rotten Swiss cheese.


Deaths rattle South Korea's seasonal flu vaccination, but authority presses ahead with free scheme

South Korea is preparing to fight two infectious diseases this winter: the novel coronavirus and the flu. But reports of deaths after flu shot vaccination may jeopardize the second effort.


As of Friday afternoon local time, 36 people have died in Korea after getting flu shots, including a 17-year-old high schooler, Korea Biomedical Review reported. Some district and municipal governments have put out requests to hospitals to suspend influenza vaccination, but the Korea Disease Control and Prevention Agency (KDCA) still wants the national program to move ahead, refuting a link between the vaccines and the deaths.

“The number of deaths has increased, but our team sees the low possibility that the deaths resulted from the shots,” KDCA Commissioner Jeong Eun-kyeong told lawmakers at a hearing on Thursday, according to Reuters. Health Minister Park Neung-hoo, for his part, promised to “thoroughly examine the entire process in which various government agencies are involved, from production to distribution.”

South Korea Officials Refuse to Suspend Flu Vaccine Program Despite 25 deaths

Flu shot halloweenNote: In case there is anyone left who thinks public health is about the public's health.

South Korea sticks to flu vaccine plan despite safety fears after 25 die

SEOUL (Reuters) - South Korean officials refused on Thursday to suspend a seasonal influenza inoculation effort, despite growing calls for a halt, including an appeal from a key group of doctors, after the deaths of at least 25 of those vaccinated.... Read more.

Evee Clobes Died 36 Hours After Her Well-Child Check-up

Evee Clobes Died 36 Hours After Her Well-Child Check-up

A Minnesota mother’s heartbreaking story and battle against corruption

MINNEAPOLIS — Oct. 21, 2020 — Evee Clobes, a healthy infant in Wright County, Minnesota, died March 1st, 2019, 36 hours after she received the CDC's recommended 6 vaccines at her 6-month well-child check-up.

“I want Evee’s story to be shared everywhere, so this never happens to another family," said Catie Clobes, Evee’s mother. To spread awareness and help secure justice for Evee, Catie, has shared her story on The Highwire with Del Bigtree; Minnesota families are wearing shirts with an emblem in the shape of a superman-like "E" and have bumper stickers on their cars; yard signs have been placed around the state; and more than 11 billboards have gone up sharing her daughter's memory and her tragic story of loss and corruption. Two massive boards are currently live off I-94 that state "36 hours after vaccines, Evee died, and the medical examiner lied."

More than 2,000 American infants die of "SIDS" every year, and parents are rightly questioning why their healthy babies suddenly died. More and more medical examiners are labeling infant deaths as "undetermined" to make it look like "SIDS" deaths are down, when infant deaths are rising.

When a patient dies after a drug overdose or medical procedure, tests are performed to rule out any and all causes of death. However, that is not the case when it comes to vaccines. Coroners aren’t even allowed to list vaccines as a cause of death. No family should have to pay for a private autopsy and fight against the medical examiner to discover that a liability free pharmaceutical product caused the death of their baby.

However, this is what Evee's mother did after Dr. A. Quinn Strobl at the Midwest Medical Examiner's office refused to run any of the requested tests, and performed a negligent, lackluster autopsy on the infant.

Justice for Evee, A Mother’s Heartbreak

On February 27, 2019, Catie Clobes brought her happy and healthy 6-month-old to her well-baby checkup, where the pediatrician declared her to be in “perfect health” with no problems or concerns. After Evee was examined by her pediatrician, the nurse administered the shots according to the CDC recommended schedule – 6 doses total – Pediarix and Prevnar.

Continue reading "Evee Clobes Died 36 Hours After Her Well-Child Check-up" »

Fake Placebo Meningitis Vaccine May Have Killed Healthy 28 Year Old Brazilian Covid Vaccine Volunteer

That's the headline Reuters should have written, instead of AstraZeneca COVID-19 vaccine trial Brazil volunteer dies, trial to continue.

Candy syringe pensIf you ask anyone with middle school grasp of science what is a "placebo," they will likely say, "a sugar pill."  A placebo has always meant an inert, benign substitute for the drug being tested.  How many Earthlings understand that with this Covid vaccine, the placebo is another vaccine? And in this case, it may well have killed a healthy, altruistic 28 year young man. Our sincere condolences to his grieving family. He volunteered to help others.   And what of every parent whose child needs a meningitis vaccine for school? Are they to feel comforted?

noun: placebo; plural noun: placebos

a harmless pill, medicine, or procedure prescribed more for the psychological benefit to the patient than for any physiological effect.
"his Aunt Beatrice had been kept alive on sympathy and placebos for thirty years"
a substance that has no therapeutic effect, used as a control in testing new drugs.
a measure designed merely to calm or please someone.
"pacified by the placebos of the previous year, they claimed a moral victory"


SAO PAULO/FRANKFURT (Reuters) - Brazilian health authority Anvisa said on Wednesday that a volunteer in a clinical trial of the COVID-19 vaccine developed by AstraZeneca and Oxford University had died but added that the trial would continue.Oxford confirmed the plan to keep testing, saying in a statement that after careful assessment “there have been no concerns about safety of the clinical trial.”

AstraZeneca declined to comment immediately.

A source familiar with the matter told Reuters the trial would have been suspended if the volunteer who died had received the COVID-19 vaccine, suggesting the person was part of the control group that was given a meningitis jab.  Read more here.

Karen Kain Continues to Fight for Vaccine Safety After Her Daughter's Death

LorrinKaren Kain's daughter Lorrin was severely injured by a routine childhoo vaccination. She died at age 15. Her mother is a powerful force in the vaccine community. Or should we say, the growing vaccine safety community? Below, she speaks out about the COVID vaccine and the PREP act which removes product liability during a pandemic.


Author: Rebecca Lindstrom
Published: 7:58 PM EDT October 8, 2020
11 Alive

ATLANTA — To build confidence in a COVID-19 vaccine, manufacturers have taken the highly unusual step of sharing their testing methods and pledged to keep politics out of the process. But the federal government is accused of doing the opposite, eroding public trust at a time when it’s needed most.

At issue, is how the government will handle adverse reactions or injuries associated with the vaccine. The US Department of Health and Human Services (HHS) plans to use the Countermeasures Injury Compensation Program (CICP).

It was created to cover damage caused by treatments for pandemics and security threats such as H1N1 and Ebola. In the past decade, 446 people filed claims, 39 were approved, but only 29 received compensation. That’s because HHS says the other 10 didn’t have any medical expenses to reimburse. In all, $5.7 million has been paid out to vaccine injured through the program.

CICP is considered a compensation program of last resort. It only pays the medical costs or lost wages that were not covered by any other program and it does not pay anything for pain and suffering.

“It is an administrative program controlled strictly by the secretary,” attorney Mike Milmoe explained.  Read more and see video at 11 Alive, Atlanta, Georgia.

1986 The Act: See the Movie Scarier than Halloween Itself For Yourself

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Covid Vaccine Adverse Reactions Euphemised to "Discomfort"

Twighlight Zone
Eye of the Beholder Episode The Twilight Zone

Imagine if you will...  your toddler wakes in the middle of the night shaking so badly that she cracks a tooth. Would you call that discomfort or call 911 for help?  Welcome to.... the CoVax Zone, where vaccine adverse reactions are pushed through like sawing off one's arm to escape a tight crevasse.  Vaccine safety is in the eye of the beholder.


CNBC: Coronavirus vaccine trial participants report day-long exhaustion, fever and headaches — but say it’s worth it

Luke Hutchison woke up in the middle of the night with chills and a fever after taking the Covid-19 booster shot in Moderna’s vaccine trial. Another coronavirus vaccine trial participant, testing Pfizer’s candidate, similarly woke up with chills, shaking so hard he cracked a tooth after taking the second dose.

High fever, body aches, bad headaches and exhaustion are just some of the symptoms five participants in two of the leading coronavirus vaccine trials say they felt after receiving the shots.

In interviews, all five participants — three in Moderna’s study and two in Pfizer’s late-stage trials — said they think the discomfort is worth it to protect themselves against the coronavirus. Four of them asked not to be identified, but CNBC reviewed documentation that verified their participation in the trials...  Read more here.Read more here.

Medford Oregon Mail Tribune Editorial on Vaccine Kool Aid

Michael Framson editorialThank you and congratulations to AofA reader Michael Framson on his published editorial in the Medford, Oregon Mail Tribune newspaper. The verbiage is below.  Brave voices speaking out in even tones, without rancor, offering information and facts is what will help Americans who are starting to question vaccine safety really listen.


The Washington Post (WAPO) editorial in the Tribune claimed that confidence in vaccines has been eroded by a “vociferous anti-vaccination movement.” Not true! Dr. Heidi Larson, PhD, Director of the Vaccine Confidence Project says the biggest factor in vaccine hesitancy is vaccine safety.

She points out at the recent WHO Vaccine Safety Summit that “doctors and nurses are ‘very wobbly’ and ‘starting to question the safety of vaccines,’ and “it's a "huge problem." In fact, “doctors don't have confidence in vaccine safety to stand up to mothers asking questions.”

WAPO, it is the vaccine science or lack thereof that has eroded the public’s vaccine confidence. As Dr. Larson points out: “There is a lot of safety science needed; “they can't keep repurposing old science that isn't relevant” to the safety questions parents are asking.

Vaccination is an invasive medical procedure using imperfect products, inadequately studied manufactured by an industry notorious for its greed, fraud, deception, lies, and prolific marketing, whether they are pushing Vioxx or vaccines. The only difference between the two is that vaccine manufacturers cannot be held accountable for their injuries and deaths.

Post, stop drinking your Kool-Aid long enough to read the science. The vociferous have.

Michael Framson
Medford, OR

Governor Cuomo Shifts from Volunteer to Anti-Vaxxer


April 2020: “It’s over whenever you have a vaccine,” said Cuomo during an Albany press briefing. He has said such a step may take 12 to 18 months. Anything we can do to work with the federal government to get the vaccine done faster, we are all in,” Governor Andrew Cuomo, New York

Gov. Cuomo: ‘I’m Not Going To Trust The Federal Government’s Opinion’ On Potential Approved COVID-19 Vaccine Governor Says New York State Health Officials Will Also Screen Any Federally Approved Vaccine

Riddle us this: Over the last year, before we had ever heard the word COVID, Governor Cuomo tightened medical exemptions and removed the religious exemption in the State of New York, in the ultimate show of vaccine trust. Removing exemptions implies that the politicians believe that every vaccine is safe and effective for every citizen. Every child. Yours. Mine. Even their own kids.  Advocates fought hard for many months to stop exemption removal laws from coast to coast. Thousands of children in New York had been expelled from school for vaccine non-compliance. Today, every parent knows what it's like to have your child home instead of in school.

This weekend, Governor Cuomo, who had at one time offered up his state to test the COVID vaccine, is now saying that he does not trust the Federal government as it generates COVID vaccines.  He wants to test it for himself in New York. But just months ago he said:

Gov. Andrew Cuomo on Wednesday offered up New York as a “laboratory” for testing of possible coronavirus vaccines, as another 752 residents succumbed to the bug. “It’s over whenever you have a vaccine,” said Cuomo during an Albany press briefing. He has said such a step may take 12 to 18 months. Anything we can do to work with the federal government to get the vaccine done faster, we are all in,” the governor continued. “We want to use New York as a laboratory. We are ready, willing, in any way.” Cuomo said the state Health Department stands ready to work with the federal Food and Drug Administration — and that New Yorkers would make perfect test subjects.  Source: New York Post April 2020


He hasn't even experienced the personal vaccine injury losses so many of us have - and he doesn't trust the science safety system. We don't trust the safety science on the pediatric schedule.  From hard experience and knowledge of the science. So let's use this opportunity to hammer home education.  Maybe COVID has a purpose after all?

National Medical Association Members Question CoVax But What About MMR

Black medical doctorWe can't help but wonder if the members of the National Medical Association, a group formed in 1895 by and for Doctors of Color,  are aware of William Thompson's information regarding the CDC and their willful altering of data to mask  the autism rate among African American toddlers based on age at which MMR was administered?  Perhaps this is a good time to reach out to them.

In June, we posted an article about Melinda Gates' announcement that African Americans should be among the first to receive the Covid vaccine, and traced her Southern, white experience in a high school that retained "slave day" as a jovial fundraiser 100 years after slavery was abolished.   Read The One In Which Melinda Gates Bestows COVID Vaccines

"The slave trade became legal for one last time ... as the Senior class members sold themselves along with thirteen brave and courageous teachers," the caption read in the yearbook, titled Acres. Two white students who darkened their skin appear in photos on the page." NBC Dallas on Melinda Gates High School Yearbook from 1979. She was a Freshman that year.


Not trusting the FDA, Black doctors’ group creates panel to vet Covid-19 vaccines

From StatNews

As trust in federal health agencies has withered over the last few months, a group of Black physicians has been working on an antidote: creating their own expert task force to independently vet regulators’ decisions about Covid-19 drugs and vaccines as well as government recommendations for curbing the pandemic.

Organized by the National Medical Association — founded in 1895 as an answer to racist professional societies excluding Black doctors — the committee is meant to safeguard against any unscientific guidance from the Centers for Disease Control and Prevention and the Food and Drug Administration.

“It’s necessary to provide a trusted messenger of vetted information to the African American community,” said Leon McDougle, a family physician and president of the NMA. “There is a concern that some of the recent decisions by the Food and Drug Administration have been unduly influenced by politicians.”

Just one of the examples he gave was the agency’s go-ahead to use hydroxychloroquine against Covid-19 even though there was no reliable evidence that it worked, and some indication that it could cause heart damage. The FDA later back-tracked and revoked the authorization.

McDougle frames the new task force as a way to address the suspicion that has sprouted up around Covid-19 vaccines. Some worry that, in being developed at “warp speed,” the shots might not be safe or properly tested before they’re approved, and the anxiety is only heightened for those who’ve been alienated by the medical system. That’s part of the reason that certain patients of color are especially wary of taking part in the clinical trials — and those concerns may well persist even if adequate studies are done and a vaccine hits the market.

“I think this will help to increase uptake in the African American community, if members of our task force give it the green light,” McDougle said. But he emphasized that their stamp of approval would come only if data show that the vaccine is, in fact, effective and safe.  Read more: Not trusting the FDA, Black doctors’ group creates panel to vet Covid-19 vaccines

Response to the British Government Proposal to Roll Out A COVD-19 Vaccine Before Christmas

image from upload.wikimedia.orgby John Stone

The British government (Prime Minister Boris Johnson pictured) are running a public consultation with a view to cutting every corner and safe-guard in order to roll out a COVID vaccine campaign before Christmas (the British “warp-speed”). presumably with the Oxford/Astra-Zeneca product in mind. For anyone who wants to respond it ends this Friday (18 September). This is how I have responded to the on-line form.

Temporary authorisation of the supply of unlicensed products

The urgency of the situation in which such a decision needs to be taken is heavily in doubt. While the government has taken it upon itself to place restrictions on the public from which it would gladly be alleviated the hospitalisation and fatality rates for the virus have been in continuous decline since the spring - if indeed there is a continuing infection rate this presumably confers more certain immunity than any putative vaccine. None of the initial candidate products purports to offer strong immunity so it is hard to see even if there were any good reasons for the present restrictions that the introduction of these products would offer sufficient grounds for their removal. It is more likely that they would simply contribute to public confusion.

As I understand it the decision to distribute unlicensed vaccines (or licensed ones) will be taken by the JCVI. The JCVI is described as an “independent” body, but of what? The chair of the JCVI, Andrew Pollard, is lead developer of the Oxford/Astra Zeneca COVID-19 vaccine, which has been backed by the government to the tune of at least £100 million. In February 2014 Pollard chaired a meeting of the JCVI which recommended the Bexsero Men B vaccine to the schedule of which he was also lead developer, which became part of Conservative window-dressing at the 2015 election. Even if Pollard recuses himself the “independence” of any decision will be in doubt - apart from anything else at its February 2016 meeting the JCVI enjoyed the hospitality of Pollard’s research institution, the Martin School, and his Oxford College, St Cross. It is not reported that any members protested. Dissent at JCVI meetings had never been reported, indeed no votes ever seem to be recorded.

Should a decision be delayed beyond the end of the year it will come under the remit of the licensing authority, the MHRA. The MHRA is entirely funded by the industry for the licensing of medicines and biologicals, and also advised by Prof Pollard. In 2009 the MHRA - at the time of the swine flu scare - failed to detect an association between the GSK vaccine Pandemrix and the condition of narcolepsy, and remained uncontrite in BMJ correspondence as late as 2018. It is illusory at the present time to suppose the licensure in itself provides grounds for confidence. The government in fact has no existing processes to ensure confidence. The government also assumes that anything “authorised” will subsequently be “licensed” which further calls the independence of the process into question. What if it turned out to be not just “temporary”

Civil liability and immunity

The document maintains that it would be unfair to manufacturers to have to sustain liability, but it is not clear why it would be fair to the public who have already had incredible costs loaded on to them, whether any suit was against the manufacturer (to be reimbursed by the government) or against the government itself, the cost of which would then be passed to the public, if successful. Admittedly, in almost any circumstances the Legal Aid Agency will fail to support such litigation (a dramatic instance would be Vioxx), so it is somewhat theoretical: whatever happens the manufacturer makes a killing and there is little sanction on them to ensure safety, let alone that you will not catch the disease.

Ultimately, the government shelters legally behind the principle of informed consent which leaves the onus on the patient or their guardian, but needs to entail that it is genuinely informed (including all the risks and shortcomings of the product as is provided in the Montgomery ruling). It is further prejudicial if scorn and loathing are heaped on anyone who is not sure whether to comply (for instance the several derogatory comments made the Prime Minister about “anti-vaxxers”, or pronouncements by the WHO about the “vaccine hesitant” being a threat to global health) which is devoid of intellectual merit, quite outside the spirit of freedom of choice or the recommendations of the recent Cumberlege review, which considered instances where injured patients were subjected to bullying tactics. This fails to recognise the rights of the patient. It also undermines the rights of the patient if they are expected to be vaccinated to protect someone other than themselves. It is not only a dubious principle it may well be that it is in the interests of children, for example, to acquire natural immunity, particularly if the virulence of the disease retreats to the level of the common cold (which seems entirely likely).

Continue reading "Response to the British Government Proposal to Roll Out A COVD-19 Vaccine Before Christmas" »

Testimony on Vaccines with Senator Rand Paul & Dr. Francis Collins

Choice_mainSenator Rand Paul on Mandated COVID Vaccination for American schoolchildren in at the HELP Hearing on 9/9. Dr. Francis Collins, the witness with whom he speaks, is the head of the NIH.  Read about the hearing here - Testimony on Vaccines: Saving Lives, Ensuring Confidence, and Protecting Public Health

"There is a difference between smallpox and COVID..."

"We really need to start thinking through our fervor."

Did Transverse Myelitis Halt the A-Z CoVax?


The New York Times reported that the Astra-Zeneca CoVax injury may have been "Transverse Myelitis." As ominous as that name sounds, the laymen's term is worse and would scare the pants off Americans: spinal cord injury.

The individual also said that a volunteer in the U.K. trial had received a diagnosis of transverse myelitis, an inflammatory syndrome that affects the spinal cord and is often sparked by viral infections. However, the timing of this diagnosis, and whether it was directly linked to AstraZeneca’s vaccine, is still unknown.

Here are excerpt from a 2009 PubMed article:  Note, the reference to the adjuvant as the possible culprit. 

Transverse myelitis and vaccines: a multi-analysis N Agmon-Levin 1 , S Kivity, M Szyper-Kravitz, Y Shoenfeld

Transverse myelitis is a rare clinical syndrome in which an immune-mediated process causes neural injury to the spinal cord. The pathogenesis of transverse myelitis is mostly of an autoimmune nature, triggered by various environmental factors, including vaccination....   ...We have disclosed 37 reported cases of transverse myelitis associated with different vaccines including those against hepatitis B virus, measles-mumps-rubella, diphtheria-tetanus-pertussis and others, given to infants, children and adults. ...The associations of different vaccines with a single autoimmune phenomenon allude to the idea that a common denominator of these vaccines, such as an adjuvant, might trigger this syndrome.

What is Transverse Myelitis?

National Institute of Neurological Disorders and Stroke

Transverse myelitis is an inflammation of the spinal cord, a major part of the central nervous system.  The spinal cord carries nerve signals to and from the brain through nerves that extend from each side of the spinal cord and connect to nerves elsewhere in the body.  The term myelitis refers to inflammation of the spinal cord; transverse refers to the pattern of changes in sensation—there is often a band-like sensation across the trunk of the body, with sensory changes below.

Continue reading "Did Transverse Myelitis Halt the A-Z CoVax?" »

President Trump Calls Vice President Biden "Anti-Vaccine"

Tweedledum Contrariwise

We are at a loss for words to explain what is happening Through The Looking Glass right now. Tighten your seat belt, all the same.

Trump blasts Biden, Harris for 'anti-vaccine rhetoric'

President Trump on Monday took aim at his Democratic opponent, former Vice President Joe Biden, and Biden's running mate, Sen. Kamala Harris (D-Calif.), over remarks by Harris that she would not take Trump's word on the efficacy of a coronavirus vaccine without assurances from top health officials.

During a press conference Monday at the White House, the president pledged that a vaccine for the coronavirus would be available in "record time," and swiped at Harris in particular over the remarks, calling her "the most liberal person in Congress."

Biden and Harris, Trump said, "should immediately apologize for the reckless anti-vaccine rhetoric that they are talking right now, talking about endangering lives. It undermines science, and what happens is all of the sudden you'll have this incredible vaccine and because of that fake rhetoric, it's a political rhetoric ... that's all that is."

Read more:  Trump blasts Biden, Harris for 'anti-vaccine rhetoric'

Taylor 2014: The International Fall-Back Position for Officials Challenged About Vaccine Safety and Autism

PS: If you find his beloved bike, please call him.

NOTE:  Excerpted with permission from Children's Health Defense.

By John Stone

Taylor 2014: The International Fall-Back Position for Officials Challenged About Vaccine Safety and Autism

This is a complementary article to JB Handley’s ‘Vaccines and Autism—Is the Science Really Settled?’ because of a parallel British experience I had. JB was bemused when he challenged Joshua Gordon, the presently appointed head of the United States about vaccines and autism, to be sent the “meta-analysis” by Taylor et al ‘Vaccines are not associated with autism: an evidence-based meta-analysis of case-control and cohort studies’. Could he do no better than that? In one respect this was consistent because this was the same study brandished by Gordon’s predecessor Thomas Insel at a 2014 Congressional hearing, when – if memory serves – Rep Posey chastised him by suggesting he might at least produce something that did not involve the research of Poul Thorsen, the former CDC employee on the run for embezzlement (whom the US government in all its might and majesty has now failed to extradite from Denmark in virtually in nine and a half years, despite being on the most wanted list).

In my case the story reaches back to November 2018 when I wrote to the British Government’s then Chief Medical Officer, Sally Davies, asking her to make good her claim that “we know” MMR “is a safe vaccine”. In response she referred me to the exact same paper Gordon cite to JB and Insel cited to Congress:

…Specifically in relation to whether MMR vaccines may be a cause of autism, a substantial body of population-based research has found no evidence to suggest a causal association. This evidence (not just for MMR, but other types of vaccine) is available for review in the published medical literature, and was summarised in a meta-analysis in 2014…

I think it is here worth mentioning that my answer (now recorded as part of an official document through Freedom of Information) was somewhat different than JB’s and therefore supplementary to it. Perhaps, when something is really rotten its rottenness may be multi-faceted, and this is what I have to add from my 2018 letter:  READ MORE AT:

Taylor 2014: The International Fall-Back Position for Officials Challenged About Vaccine Safety and Autism

58% of Americans are Anti-Vaxxers

Big League Politics Yahoo reports: Yahoo News/YouGov coronavirus poll: Number of Americans who plan to get vaccinated falls to 42% — a new low   Americans do not trust the rushed vaccine in either party. Because we're pretty smart people no matter how we vote.  Even experts are speaking out:

“Why should we expect Americans to agree to a vaccine before one is even available?” coronavirus expert Natalie Dean, an assistant professor of biostatistics at the University of Florida, recently wrote in the New York Times. “I’m a vaccine researcher, and even I would place myself in the ‘not sure’ bucket. What we have right now is a collection of animal data, immune response data and safety data based on early trials and from similar vaccines for other diseases. The evidence that would convince me to get a COVID-19 vaccine, or to recommend that my loved ones get vaccinated, does not yet exist.”

I don't buy the political division - do you?

The outlook for universal vaccination is clouded by political considerations from both sides: skepticism about medical authority and expertise (more common among Trump supporters), and suspicions (mostly among Democrats) that the administration is cutting corners on safety to rush a vaccine into production before the election.

Guilt, Anger, Economic Freedom, Non-Bravery? Government Testing at Yale on Covid Shot Messaging

Red white blue vaccineWho wants to see the sausage being made? Below are excerpts and a link from the study being conducted by YALE testing which messages will convince Americans to take the Covid shot(s.)

COVID-19 Vaccine Messaging, Part 1:


This study tests different messages about vaccinating against COVID-19 once the vaccine becomes available. Participants are randomized to 1 of 12 arms, with one control arm and one baseline arm. We will compare the reported willingness to get a COVID-19 vaccine at 3 and 6 months of it becoming available between the 10 intervention arms to the 2 control arms.

Study participants are recruited online by Lucid, which matches census based sampling in online recruitment.

Other: Control message Other: Baseline message Other: Personal freedom message Other: Economic freedom message Other: Self-interest message Other: Community interest message Other: Economic benefit message Other: Guilt message

1/15 of the sample will be assigned to this message. The message is about the danger that COVID-19 presents to the health of one's family and community. The best way to protect them is by getting vaccinated and society must work together to get enough people vaccinated. Then it asks the participant to imagine the guilt they will feel if they don't get vaccinated and spread the disease.
Other: Embarrassment message

1/15 of the sample will be assigned to this message. The message is about the danger that COVID-19 presents to the health of one's family and community. The best way to protect them is by getting vaccinated and by working together to make sure that enough people get vaccinated. Then it asks the participant to imagine the embarrassment they will feel if they don't get vaccinated and spread the disease.
Other: Anger message Other: Trust in science message Other: Not bravery message

1/15 of the sample will be assigned to this message which describes how firefighters, doctors, and front line medical workers are brave. Those who choose not to get vaccinated against COVID-19 are not brave.


Alan Dershowitz and Robert Kennedy Jr Debate

Thank you tupeThank you to Professor Alan Dershowitz for having the chutzpah to debate vaccination policy, safety and mandates with Robert Kennedy, Jr. yesterday.  He's the first national figure to enter into a civil, rational and yes, heated conversation on the controversial topic.  Love him or not so much for his controversial clients including OJ Simpson, Claus Von Bulow and even Jeffrey Epstein, Professor Dershowitz is a powerful figure in American law. As is Mr. Kennedy. We hope that he spent more than a few sleepless moments last night mulling over what he learned. He'd be a formidable ally.  Watch below.

Vaccine Debate Is On! Robert F. Kennedy, Jr. vs Alan Dershowitz

Note: We'll follow up with where and how to watch before the event. Here you go!


From CHD: Don’t miss this historic debate between Children’s Health Defense Chairman Robert F. Kennedy, Jr. and Harvard Law Professor Alan Dershowitz.

With the current COVID crisis dominating headlines at national and local levels, the topic of vaccines is now front and center. The two attorneys will debate a range of issues including vaccine mandates, the PREP Act, the lack of vaccine safety studies, Jacobson vs. Massachusetts, and HHS’s failure to act on provisions of the National Childhood Vaccine Injury Act. Are compulsory vaccines even legal? Should any government be able to force medical procedures on families?

Tune in July 23, 2020 8:45 a.m. EST / 7:45 a.m. CST / 5:45 a.m. for insightful discussions on these questions and more.

Please slow down"Disturbing??" We think not. This is hopeful! Let's focus on PREVENTION and then TREATMENT. Of the nine people I know personally who have had COVID, none were hospitalized. Two (over the age of 60) had a couple of rough days at home, one is 8 months pregnant with no symptoms, the others reports mild fever and discomfort for a couple of days.  All of them are fit, low BMI, no major pre-existing conditions.  It seems the loss of smell and taste most of them reported is rotten indeed. A friend's Grandfather contracted COVID because he was placed in a rehab center loaded with it after a successful, not COVID surgery.  He was in his mid 90s and passed away after about 6 weeks. Whom do you know who has contracted COVID?


SF Chronicle:

With coronavirus antibodies fading fast, vaccine hopes fade, too

Disturbing new revelations that permanent immunity to the coronavirus may not be possible have jeopardized vaccine development and reinforced a decision by scientists at UCSF and affiliated laboratories to focus exclusively on treatments.

Several recent studies conducted around the world indicate that the human body does not retain the antibodies that build up during infections, meaning there may be no lasting immunity to COVID-19 after people recover...

'Grave disservice': Merck CEO warns against virus vaccine hopes

Ken Frazier
Kenneth Frazier, Merck CEO

Note: We have the best readers. Thank you ME for sending me this article from Al Jazeera.  I had to read it a couple of times, I thought maybe I was being punked.


'Grave disservice': Merck CEO warns against virus vaccine hopes

Head of US pharmaceutical giant says health officials may not be able to distribute coronavirus vaccines widely enough.

Coronavirus vaccines under development are not guaranteed to work, and people who raise hopes of developing a vaccine before year-end are doing a "grave disservice to the public", Merck & Co Inc's chief said, according to a Harvard Business Review report.

The potential vaccines may not have the qualities needed to be rapidly deployed in large numbers, Chief Executive Kenneth Frazier said in an interview published on Monday.

"If you're going to use a vaccine on billions of people, you better know what that vaccine does," he was quoted as saying.

A United States official said Monday that drugmakers partnered with the US government are on track to begin actively manufacturing a COVID-19 vaccine by the end of the summer, Reuters reported.

The Trump administration aims to produce 300 million vaccine doses by the end of 2021 through its Operation Warp Speed Program.

Some previous vaccines "not only didn't confer protection, but actually helped the virus invade the cell, because it was incomplete in terms of its immunogenic properties," Frazier said. "So we have to be very careful."  Read more here.

No Data for Neurological Impairment

John Stone Twitter Exchange
Our John Stone asked a simple, but critical question of Danish Professor Dr. Christine Stabell Benn on Twitter. "Do you have data for neurological impairment" from pediatric vaccines. In other words,  "At what cost?" And the answer was, “No, the focus is on the overall effect of vaccines on mortality and morbidity."  Or, " We don't know and we haven't bothered to look." I looked up the definition of the two terms:  Mortality is death. Morbidity is sickness or illness, but apparently only from the virus IN the syringe, not caused by it. 

ACOG Wants CDC To Test Covid Vaccines on Pregnant Women of Color

"It's a psychological fact. Pleasure helps your disposition." 
Camel Cigarette ad. So puff away!  1950

"We're making sure this a psychological fear tactic. Covid could kill your baby."
American College of Ob and GYN. So test this new vaccine! 2020


"It's a psychological fact. Covid will kill your baby." So test this new vaccine! 2020

My oldest daughter is 25. My youngest is almost 20. During my three pregnancies, women were outright shamed for having a sip of champagne at a wedding, a taste of coffee at breakfast, a bite of a tuna sandwich at lunch, a puff of a cigarette any time, a tablet of Tylenol for a headache, a spoonful of any medicine whether OTC or Rx. Vaccines, let lone experimental vaccines, were never, ever mentioned to me in 27 months of pregnancy (3 kids, I'm not an elephant.)

OB/GYN Docs in U.S. Want COVID-19 Vaccines Tested on Pregnant Women

Below is an excerpt from OB/GYN Docs in U.S. Want COVID-19 Vaccines Tested on Pregnant Women
by Barbara Cáceres
Published July 6, 2020 | Medicine, Women

The Vaccine Reaction

ACOG Says Pregnant Women, Breastfeeding Moms Should Be Test Subjects in COVID-19 Vaccine Trials and Be Among the First to Get Vaccinated

In its June 24 statement, the ACOG also stated:

In light of this new information from the CDC regarding the risk to pregnant patients, it is even more concerning that pregnant and lactating patients have been excluded from clinical trials for a coronavirus vaccine. The new information from the CDC highlights the importance of pregnant patients being prioritized for a coronavirus vaccine once it becomes available. ACOG again urges the federal government to use its resources to ensure the safe inclusion of pregnant and lactating patients, including patients of color, in trials for vaccines and therapeutics to ensure that all populations are included in the search for ways to prevent and treat COVID-19.13

Questions About Safety of Vaccination During Pregnancy

The time-honored rule of avoiding any potential toxic exposure that might interfere with the normal development of the fetus was suspended and replaced by the CDC in 2006 with an assumption that vaccination during pregnancy was safe after the CDC strengthened recommendations that all pregnant women, healthy or not, should get influenza vaccine during in any trimester. This CDC recommendation was followed up in 2011 with another new one directing obstetricians and gynecologists to administer a pertussis containing Tdap (tetanus, diphtheria and pertussis) shot to all pregnant women during every pregnancy.14 15    

Read more at:
OB/GYN Docs in U.S. Want COVID-19 Vaccines Tested on Pregnant Women

WHO Document: Draft landscape of COVID-19 candidate vaccines

World Health Org WHOIn the USA, we're in a contentious Presidential election cycle. Speaking of candidates,  attached is  a document from WHO that provides a chart of the current COVID-10 vaccine candidates.  Can we write in, "no thanks?"

Draft landscape of COVID-19 candidate vaccines

These landscape documents have been prepared by the World Health Organization (WHO) for information purposes only concerning the 2019-2020 global of the novel coronavirus. Inclusion of any particular product or entity in any of these landscape documents does not constitute, and shall not be deemed or construed as, any approval or endorsement by WHO of such product or entity (or any of its businesses or activities). While WHO takes reasonable steps to verify the accuracy of the information presented in these landscape documents, WHO does not make any (and hereby disclaims all) representations and warranties regarding the accuracy, completeness, fitness for a particular purpose (including any of the aforementioned purposes), quality, safety, efficacy, merchantability and/or non-infringement of any information provided in these landscape documents and/or of any of the products referenced therein. WHO also disclaims any and all liability or responsibility whatsoever for any death, disability, injury, suffering, loss, damage or other prejudice of any kind that may arise from or in connection with the procurement, distribution or use of any product included in any of these landscape documents.

New Polls Show Skepticism of COVID Vaccine

Ask questionPublic Health and the media have long considered anyone who questions vaccine safety to be an "anti-vaxxer." As the world has been turned inside out because of COVID-19, people who likely never questioned pediatric vaccines are beginning to wonder how a rushed COVID vaccine can be safe and effective.  People in droves are asking hard questions about a rushed vaccine that has been touted as the one and only path to a "new COVID normal."  We're going to need a much bigger tent for the anti-vaxxer holiday party....  


'Anti-vaxx' influence means up to half may not take coronavirus vaccine New polls in the US, Germany and the Czech Republic - among others - found that 50 per cent were sceptical

New polls in the US, Germany and the Czech Republic - among others - found that 50 per cent were sceptical.

Up to half of the populations in countries including the United States, Germany and the Czech Republic say they may not get any new coronavirus vaccine that is developed.

A vaccine against the deadly virus that has swept the globe over the last six months is seen as possibly the only way for the world to return to normal after the pandemic, and scientists in hundreds of different countries are working as fast as they can to try to produce one.

However, experts have estimated that at least 70 per cent of people will have to get the vaccine in order for it to stop coronavirus, a figure that appears to be some way off based on the latest numbers.

Professor Heidi Larson, anthropologist and director of the Vaccine Confidence Project at the London School of Hygiene and Tropical Medicine, said: "It's going to be a challenge, particularly because in general, populations are more anxious about new vaccines and that's understandable.

"But the good news is we do have time before we, hopefully, get a vaccine, so I think that we have to use that."

In the United States, a number of polls have shown that only around 50 per cent are committed to getting a coronavirus vaccine...

This week, the country's leading public health expert Dr Anthony Fauci told CNN he believed that the US was "unlikely" to reach herd immunity as a result of this, inspired by the "general anti-science, anti-authority, anti-vaccine feeling".

In Germany, a poll this week by YouGov found that only one in two Germans would definitely get vaccinated if there was a jab available, and one in five said they definitely would not. A protest was held in Ukraine on Friday over the potential for compulsory coronavirus vaccinations...

WHO's lead scientist Soumya Swaminathan places chief hope in Oxford and Moderna vaccines

image from www.fic.nih.govHaving systematically screwed up the hydoxychloroquine (HCQ) trials for the treatment of the Covid virus and otherwise prevented its general use, all of which likely ended up in countless unnecessary deaths (see Dr Meryl Nass's despairing assessment) the WHO are now turning their attention to the first crop of vaccines, created at reckless speed with new technologies. The WHO's chief scientist told Reuters on Friday:

GENEVA (Reuters) - AstraZeneca's <AZN.L> experimental COVID-19 vaccine is probably the world's leading candidate and most advanced in terms of development, the World Health Organization's (WHO) chief scientist said on Friday.

The British drugmaker has already begun large-scale, mid-stage human trials of the vaccine, which was developed by researchers at University of Oxford.

This week, AstraZeneca signed its tenth supply-and-manufacturing deal.

"Certainly in terms of how advanced they are, the stage at which they are, they are I think probably the leading candidate," WHO chief scientist Soumya Swaminathan told a news conference.

The Oxford vaccine has a shaky history, funded to the tune of £90m million by the British government and taxpayer, and already in manufacture in billions of doses, the human trials began in April amid false reports that the animal trials had been successful: the product is arguably commercially too big to be allowed to fail. It also has the advantage that its lead developer Andrew Pollard heads the committee that will advise the British government on its use. Admittedly, last week he was in an apparently non-committal mood in conversation with Prince William:

Prof Pollard highlighted HIV, a virus for which no vaccine has been found because it mutates, saying scientists' great fear was that coronavirus could be the same. In that case, he said 'there is nothing we could do apart from social distancing forever' - a prospect William described as 'frightening'.

Continue reading "WHO's lead scientist Soumya Swaminathan places chief hope in Oxford and Moderna vaccines" »

Kennedy Tells How Vaccine Safety Commission Pfizzled When Pfizer Got Into Trump Administration

Fox-In-The-HenhouseSo much for draining the swamp. When President Trump appointed (was handed on a silver platter atop one million dollars) Scott Gottlieb to run the FDA, that was the death knell for the Vaccine Safety Commission he promised Americans. The pfox sashayed into the hen house with a million bucks and had a fine meal, leaving not so much as a feather. Kennedy on safety commission

America's Skepticism of Operation Warp Speed Is Not Our Fault

Id buy that for a dollar
Source: RoboCop

Note: When I was a young woman, I remember my Dad telling me he never, ever bought a car in its first model year, no matter how snazzy or how much he wanted that shiny new GM. He said it took time to work out the kinks.

Many Americans are worried that a brand new, rushed and liability free COVID vaccine might not be safe. It's natural to worry. It's smart to worry. People who have never, ever questioned vaccines are perking up. ON THEIR OWN. We are not a club seeking fresh members. Enable us? Such nonsense. Dr. Hotez also blames the way the vaccines are being "communicated." In other words, they need a better AD CAMPAIGN. Better "optics" to use today's parlance.


'Operation Warp Speed' is fueling vaccine fears, two top experts worry

The federal government's "Operation Warp Speed" vaccine program, with its emphasis on quick production and testing of experimental coronavirus vaccines, is fueling fears already stirred up by vaccine skeptics, two experts said Friday.
The approach itself is not unreasonable, said Dr. Peter Hotez, dean of the National School of Tropical Medicine and professor of pediatrics and molecular virology and microbiology at Baylor College of Medicine. But the way it's being communicated is scaring people, he told CNN.

"The way the message is coming out of Operation Warp Speed creates a lot of chaos and confusion. And it is enabling the anti-vaccine movement," Hotez said.A White House coronavirus task force source told CNN earlier this week that the Trump Administration's Warp Speed program had chosen five companies mostly likely to produce a Covid-19 vaccine -- whittled down from 14 last month when "Operation Warp Speed" was launched.

Coronavirus Vaccine Poll Results Show National Skepticism


Well, fellow anti-vaxxers, looks like we're gonna need a bigger boat....  ONLY 27% of Americans say they WOULD (doesn't mean will, would brings in conditions, I would... IF) take the brand new, wet behind the ears, greenhorn, new kid on the block, untested, experimental Coronavirus vaccine that may or may not ever even see the light of day. YouTuber and child Re-home-girl Myka Stauffer is rumored (we're kidding) to say she will only take the vaccine during an unboxing segment at $1.00 per view. A plurality is simply the largest number in a poll - it does not mean a majority.  The article also neglects to point out the MMR uptake is high because it is on the pediatric schedule.

From ABC News:

27% unlikely to be vaccinated against the coronavirus; Republicans, conservatives especially: POLL

Unpersuaded by more than 100,000 pandemic deaths in the United States, 45% of strong conservatives, four in 10 Republicans and nearly as many evangelical Christians say they’d be unlikely to get vaccinated against the coronavirus, even for free.

Overall, 27% of adults in an ABC News/Washington Post poll say they definitely (15%) or probably (12%) would not get the vaccine. Among them, half say they don’t trust vaccines in general, while nearly a quarter don’t think it’s needed in this case.

A plurality definitely would get vaccinated (43%) and 28% say they probably would. The net, 71%, is much higher than the adult vaccination rate for the standard seasonal flu – 45% in the 2018-19 flu season, according to the U.S. Centers for Disease Control and Prevention (with a wide range by state, from 34 to 56%.) It’s much lower than the 2017 child vaccination rates for polio and measles/mumps/rubella, 93 and 92%, respectively.  Read more at the link below.

27% unlikely to be vaccinated against the coronavirus; Republicans, conservatives especially: POLL

Moderna Religion and the COVID-19 Vaccine Trial

Our Father WHO art in CDC, hallowed be thy name.
Thy vaccine come. Thy liability none.
On Earth as it is your fairytales.
Give us this day our daily dose and forgive us our questions
As we destroy those who have questioned before us
Lead us not into anti-vaccination
But deliver us from disease.

From the StatNews article below: He (Moderna test subject Ian Haydon) and his girlfriend arrived home at 7 a.m., and he slept until noon. His temperature was 101.5. He got up to go to the bathroom, and became so nauseous he threw up. On his way back from the bathroom, he fainted. His girlfriend caught him and kept his head from hitting the floor. 

Do you have someone around at all times to keep your head from hitting the floor? Perhaps in addition to $1,200 to keep us afloat, Americans need funds to hire a CoVax Buddy.  On Twitter, Ian Haydon said, "-- deep breath - I had a bit of an issue..."  And Moby Dick was a bit of a whale.  Keep all of the test subjects in your thoughts. We know what can happen, after all.



By Matthew Herper. Stat News:

He experienced a severe reaction to Moderna’s Covid-19 vaccine candidate. He’s still a believer

Patients in clinical trials are usually faceless. But as the experimental Covid-19 vaccine being developed by Moderna Therapeutics has begun advancing through studies, it has found a much more visible advocate: trial volunteer Ian Haydon, a 29-year-old in Seattle.

Haydon has spoken about the vaccine on CNN and CNBC. He even said he’d volunteer to be exposed to the novel coronavirus, SARS-CoV-2, if researchers want to test to see if the vaccine was actually effective. But up until now he has left out a key detail: He is, apparently, one of three people in the trial who had a systemic adverse reaction to the vaccine. 

Twelve hours after receiving his second dose, he developed a fever of more than 103 degrees, sought medical attention, and, after being released from an urgent care facility, fainted in his home. He recovered within a day.

He has not brought up the side effects previously, he said, out of “an abundance of caution.”

“I understand that sharing the story, it’s going to be frightening to some people,” he said. “I hope that it doesn’t fuel any sort of general antagonism towards vaccines in general or towards even this vaccine....  Read more here.


Further Anomalies of the Oxford Coronavirus Vaccine

image from upload.wikimedia.orgby John Stone

On 27 April a New York Times article reported excitedly the result animal trials of the Oxford Coronavirus vaccine:

"Scientists at the National Institutes of Health’s Rocky Mountain Laboratory in Montana last month inoculated six rhesus macaque monkeys with single doses of the Oxford vaccine. The animals were then exposed to heavy quantities of the virus that is causing the pandemic... But more than 28 days later all six were healthy, said Vincent Munster, the researcher who conducted the test.."

This would have been just as well because just four days earlier on 23 April Oxford Vaccine Group under the leadership of Andrew Pollard amid immense publicity had begun experimenting on human subjects. On 30 April a contract was announced with AstraZeneca to manufacutre the vaccine, promising to deliver an entirely new vaccine to the market at unprecedented speed by September. The only trouble was that when the results of the animal trial came to light in mid-May it was disclosed that on the contrary all the monkeys had  become ill. The Daily Mail reported:

"In the latest animal trials of the vaccine carried out on rhesus macaques, all six of the participating monkeys went on to catch the coronavirus.

"Dr William Haseltine, a former Harvard Medical School professor, revealed the monkeys who received the vaccine had the same amount of virus in their noses as the three non-vaccinated monkeys in the trial.

This suggests the treatment, which has already received in the region of £90 million in government investment, may not halt the spread of the deadly disease."

Haseltine also commented in Forbes:

"There is a second troubling result of the Oxford paper. The titer of neutralizing antibody, as judged by inhibition of virus replication by successive serum dilutions as reported is extremely low. Typically, neutralizing antibodies in effective vaccines can be diluted by more than a thousand fold and retain activity. In these experiments the serum could be diluted only by 4 to 40 fold before neutralizing activity was lost."

Manifestly, human testing proceeded both against an entirely misleading background, and prematurely - which poses the most serious ethical questions. And now that we know that though the product was defective everything ploughs on regardless - Oxford/AstraZeneca now have contracts for hundreds of millions of rounds of the vaccine from both the British and the United States government.The British government has both a huge financial investment in the product and a reputational one, but it may help that Prof Pollard is both an adviser to the British regulator and chair of the committee recommends vaccine for public use.

John Stone is UK Editor for Age of Autism.




Robert Kennedy Jr "The government has been trying for almost thirty years to develop a Coronavirus vaccine..."

Dead ferretTranscribed by Anne Dachel. Robert Kennedy Jr tells about the horrible death of Ferrets used to test previous versions of a

(VIDEO) May 22, 2020, Joni Table Talk:

 The Coronavirus Vaccine Uncensored | Robert F. Kennedy Jr. & Del Bigtree

Robert Kennedy, Jr.:  “The government has been trying for almost thirty years to develop a coronavirus vaccine, and it’s been unsuccessful.

“Beginning in 2002 there were three outbreaks of coronavirus. We called them SARS at that point and MERS.

“The first SARS was a natural illness. It jumped from a bat to human beings. The second two were lab created that escaped and infected human beings. So the governments of China and a consortium of western governments all got together and put millions and millions of dollars into an effort to develop a coronavirus vaccine.

“Between 2002 and 2012, 2014, they worked very hard to do that, and what happened is they developed about 35 vaccines. Four of them were really promising. They chose the four most promising, and they gave them to ferrets, which is the animal that is most analogous when it comes to upper lung respiratory infections.

“The ferrets had a brilliant, robust and durable antibody response. Then something horrible happened. When those ferrets were challenged, when they were exposed to the wild virus they got horribly sick. They got inflammation throughout their bodies, and they died.  (See Pubmed NIH: Severe Acute Respiratory Syndrome Vaccine Efficacy in Ferrets: Whole Killed Virus and Adenovirus-Vectored Vaccines )

“The scientists remembered that something very similar had happened in the 1960s where they had developed a virus for RSV, which is very similar to coronavirus. It’s an upper respiratory infection, ailment.

“They had skipped the animals and given them directly to 35 children, and the children again had developed a very robust antibody response. But when those children were exposed to the wild virus, they got very, very sick, much sicker than the unvaccinated children. And two of those kids had died. It was a scandal.

Continue reading "Robert Kennedy Jr "The government has been trying for almost thirty years to develop a Coronavirus vaccine..."" »

Moderna Failed to Bring a Single Product to Market in 10 Years; Until Covid

95038792-BD38-4304-8EDA-E51AF62EB156 The media is reporting that  Moderna has had a successful early phase creation of a COVID vaccine.

From NBC:

Moderna: Early coronavirus vaccine results are encouraging

The vaccine seems safe, the company said, but much more extensive testing is needed to see if it remains so. A high dose version is being dropped after spurring some short-term side effects.

According to Wiki,  As of May 2020, none of its products have reached the final phase of a clinical trial, received approval by the FDA or been sold on the market, We know all too well, that Wiki can lie. However, imagine your very first success being the COVID vaccine. This is like getting sex tips from the 40 year old Virgin. This early report does not mean Moderna will bring a vaccine to market. But if they do, it will be their debut. And all of the liability will be on.... you.

Several companies are in the race to create "the vaccine" including Johnson & Johnson. Time will tell who "wins." 

WebMD: A COVID-19 Vaccine by Fall Is Possible, But at What Cost?

Speak_out_for_safety_osha_caution_signBy Dennis Thompson
HealthDay Reporter

Don't clean your screen or call your optometrist, you read that correctly: WebMD is questioning the safety of a rushed COVID vaccine.

A COVID-19 Vaccine by Fall Is Possible, But at What Cost?

MONDAY, May 11, 2020 (HealthDay News) -- Efforts to create a COVID-19 vaccine are proceeding at an unprecedented pace, with eight different candidates now being tested in humans around the world.

But to have a vaccine available for widespread use by early next year could entail bending some rules regarding safety and testing -- actions that might put the health, and possibly the lives, of test volunteers at risk.

"It is possible to have a vaccine by the fall or winter," said Dr. Greg Poland, director of the Vaccine Research Group at the Mayo Clinic in Rochester, Minn. "It is not possible to have a vaccine by fall or winter that has gone through the usual safety testing. Speed is a tradeoff with safety."

The government's leading vaccine expert -- Dr. Anthony Fauci, director of the U.S. National Institute of Allergy and Infectious Diseases -- raised eyebrows in late April when he declared it "doable" to have millions of doses of coronavirus vaccine ready for distribution by January.

"We have to remember that the fastest we've ever seen this really being done is four years," said Dr. David Shulkin, former secretary of Veterans Affairs and former president and CEO of Beth Israel Medical Center in New York City. "The traditional methods and processes for developing vaccines take a great deal of time."

However, Shulkin and other experts agree that a COVID-19 vaccine could be ready for public distribution earlier than the 12- to 18-month development timetable that has been suggested.

The holdup isn't in creating a vaccine. The World Health Organization lists eight candidate vaccines currently in human clinical trials, and 100 more candidates are undergoing preclinical evaluation in laboratories worldwide.

Rather, testing each vaccine to make sure it's safe and effective is what eats up months and years, Shulkin said during a HealthDay Live Stream interview.

"It's likely we will see vaccine approvals outside the United States -- where the regulatory approvals may not necessarily be as stringent -- in a quicker time period than even the 18-month period we've discussed," Shulkin said.  Read more here.

April 4 Expert Panel on COVID-19 & The Vaccines To Follow

Thank you to our Anne Dachel for transcribing excerpts for our readers.  Anne says:

"This was one of the most informative and empowering talks I’ve ever listened to in all the years I’ve been working as an autism advocate. Every person concerned about what the COVID 19 pandemic will do to our medical freedom needs to hear these speakers and learn the truth about what’s coming. There is no walking away from this threat to our liberties."

April 4, 2020, Panel discussion the COVID 19 crisis and what a vaccine could mean to the American people.


Dr. Andrew Wakefield, Dr. Judy Mikovits, Del Bigtree, Ty and Charlene Bollinger, Robert Kennedy, Jr., Dr. Sherri Tenpenny, Dr. Rashid Buttar.

Here are excerpts from the discussion.

Charlene: “…the year 2020 was a big deal. … This is the year, if we don’t help people understand this critical issue we may loss our freedoms, and they may be able to come in and try …to force us into these vaccines. But we did not know what we were getting into….

“I was watching Tucker Carlson  [Fox, Tucker Carlson Tonight]. He’s actually had Bobby Kennedy on…  We couldn’t believe that mainstream media outlet was covering that. We felt like Tucker’s our friend…

“Last night…on Tucker Carlson Tonight … He had a guest and they talked about Operation Wrap Speed, the COVID vaccination where they’re literally going to pass through the trials that they should be doing. They’re going to skip all that safety measures to get to this vaccine. They’re going to have a hundred million ready to go. …

“The guest talked about this as if it’s a good thing, and Tucker Carlson who has interviewed our good friend Bobby Kennedy, ….  I was really letdown by the fact that Tucker Carlson allowed that guest to say that and didn’t dig in. …”

5:42 Kennedy: “There’s now eighty separate vaccine projects. Bill Gates has eight of them. Bill Gates is now the biggest vaccine producer in the world, bigger than any other company.

Continue reading "April 4 Expert Panel on COVID-19 & The Vaccines To Follow" »

Bloomberg Admits Drugmakers Including Pfizer Are Compromising Safety For Rush To Market

DD2BE9B1-00E2-425A-ABBA-01552728CA0BYesterday was the 59th anniversary of the first American manned space flight by Alan Shepard. Now imagine that NASA was granted the power to demand that EVERY AMERICAN take a space flight starting on May 6th, 1961. THAT's the COVID vaccine.  For some, the vaccine might be a giant leap for health. For others? A Challenger far worse.

Pro-vax. Anti-vax. Doesn’t matter. Bloomberg is telling you that safety for a product already exempt from liability, safety is not the very first priority.   Anyone who takes the new vaccine will be participating in the world's largest clinical trial. "Vaccine trials normally start by looking at safety, but in order to hasten the development of a Covid-19 vaccine, the drugmakers are looking at both safety and the immune-system response from the experimental shots."

In March, Wayne Rohde wrote an article for us titled Meet The PREP "Public Readiness and Emergency Preparedness" ActMeet The PREP "Public Readiness and Emergency Preparedness" Act:  Here is the definition of the act. The Public Readiness and Emergency Preparedness Act (PREP Act) added new legal authorities to the Public Health Service (PHS) Act to provide liability immunity related to the manufacture, testing, development, distribution, administration and use of medical countermeasures against chemical, biological, radiological and nuclear agents of terrorism, epidemics, and pandemics.   It also added authority to establish a program to compensate eligible individuals who suffer injuries from administration or use of products covered by the PREP Act’s immunity provisions.

Bloomberg News published an article yesterday about the race to bring COVID-19 vaccines to market.  Below is an excerpt and link. And I've taken a screen shot to preserve the critical phrasing.

Pfizer Starts U.S. Trials of Experimental Covid-19 Vaccine By Cynthia Koons

...New York-based Pfizer is working with BioNTech SE of Germany. The companies started testing the inoculations in patients in Germany in late April. Vaccine trials normally start by looking at safety, but in order to hasten the development of a Covid-19 vaccine, the drugmakers are looking at both safety and the immune-system response from the experimental shots.

Pfizer and BioNTech are in a race with companies including Johnson & Johnson, Moderna Inc. and dozens of other biopharmacuetical outfits and academic groups to come up with a safe and effective vaccine against the illness within the next year to 18 months. A handful are in human trials already, including Moderna’s and ones from CanSino Biologics Inc., the Beijing Institute of Biotechnology and Inovio Pharmaceuticals Inc.

Pfizer’s U.S. trial will involve 360 patients in two age groups: 18 to 55, and 65 to 85, though trials in the older population will start only after safety and immune response are established in the younger group. The University of Rochester Medical Center/Rochester Regional Health and Cincinnati Children’s Hospital Medical Center will eventually provide testing sites for the vaccines as well.

Continue reading "Bloomberg Admits Drugmakers Including Pfizer Are Compromising Safety For Rush To Market" »


image from pbs.twimg.comby John Stone

This is  the letter I sent to my Member of of Parliament yesterday forwarding the excellent  letter to the UK's Secretary of Health and Social Care, Matt Hancock (pictured with Bill Gates),  by Robert Verkerk and Damien Downing:

Dear ------,

I am forwarding the excellent letter (attached) to Matt Hancock by Robert Verkerk of the Alliance for Nautal Health International and Damien Downing of the British Society for Ecological Medicine requesting transparency over the introduction of any COVID-19 vaccines in response to the current crisis, and I would suggest that it is necessary for the Secretary of State to make clear undertakings rather than vague professions of good faith. The letter can be found here on-line [1]. 
It was well understood even in the 19th century how statistics could be distorted for political purposes, since when the methods have only become more sophisticated and ultimately potentially more obfuscating. The safety, usefulness and effectiveness of universal vaccines should have to be meticulously and transparently established, yet we advance at reckless pace. It is certain that none of the candidates will have long term testing and it is questionable who on the face of it they could sensibly be given to [2].
There are other matters of transparency which go beyond the Verkerk/Downing letter. For example, the unusual arrangement by which the Secretary of State is also the main shareholder in the Porton Down Lab (as is now well-known). It was distressing to see how the Secretary of State began pumping public money into the speculative Porton Down vaccine project in the early stages of the epidemic, while failing to ensure that the puplic were immediately protected [3] (we are now heading for the worst fatality rate of any country). On the 19 March Public Health England put out a statement that they no longer considered COVID-19 to be a high risk disease [4] and within a day we were facing lockdown. Not much more convincing, now, are tub thumping references to British innovation by the Business Secretary or the Prime Minister.

Continue reading "A Letter to My Member of Parliament: THE CRITICAL NEED FOR TRANSPARENCY AROUND COVID-19 VACCINES" »

The Dengvaxia Disaster Was Twenty Years in the Making—What Will Happen With a Rushed COVID-19 Vaccine?

DengvaxiaEditorial by Lyn Redwood, President, Children’s Health Defense

Article that follows by the Children’s Health Defense Team

The Dengvaxia Disaster Was Twenty Years in the Making—What Will Happen With a Rushed COVID-19 Vaccine?

Vaccine development is a topic that is on the minds of everyone as the world grapples with ways to protect our health and the health of our loved ones from coronavirus. The team at Children’s Health Defense decided to write an article about Dengue Fever because an important part of medicine’s body of knowledge comes from the opportunity to learn from past mistakes.

Dengue fever is a common disease in more that 120 countries and, like Coronavirus, has been the target for a vaccine for many years. The development and licensure of Dengvaxia® vaccine by Sanofi  spanned more than 20 years and cost more than 1.5 billion U.S. dollars. But the development of the vaccine turned out to be tricky. Dengue vaccine antibodies can also make the infection worse, especially in infants and children who have never been exposed to the virus. The virus may actually use the antibodies created by the vaccine to spread the virus throughout the body. So an infection with dengue — when your blood already has antibodies in it — can actually enhance the disease resulting in deadly complications.

Despite the fact that Sanofi tested Dengvaxia in several large clinical trials with more than 30,000 kids globally and published the results in the prestigious New England Journal of Medicine, there were serious problems. According to epidemiologists who reviewed the data, the trials were riddled with “small inaccur­acies, missing data, and uncalculated risks.” Buried in those clinical trials was a disease enhancement safety signal, but industry and the World Health Organization (WHO) turned a blind eye to the problem, calling it a “theoretical possibility.”  Dengvaxia was subsequently admini­ster­ed to thousands of children in the Philippines. It was reported last year that the deaths of approximately 600 children who received the vaccine are under investigation by the Public Attorney’s Office. The vaccine has been permanently banned in the country.

What is also very concerning is that even after Dengvaxia led to tragic injuries and deaths in the Philippines, the FDA moved forward and licensed the vaccine in the U.S. According to a May 1, 2019 press release, the agency granted the application Priority Review under a program intended to encourage development of new drugs and biologics for the prevention and treatment of certain tropical diseases. Such actions by the FDA raise serious questions about safety, not only for the Dengue vaccine, but for future vaccines in development.

Continue reading "The Dengvaxia Disaster Was Twenty Years in the Making—What Will Happen With a Rushed COVID-19 Vaccine?" »

British Government Plays With Fire Over COVID-19: Enter Prof Pollard

image from en.wikipedia.orgby John Stone

Next week Over Vaccine Group begin human testing for a COVID-19 vaccine with a with a view to marketing by the autumn. The speed of the process may be accelerated by the fact that Professor Pollard who heads the OVG is also advisor to the the UK's licensing body, the MHRA, and chair of the JCVI, the body which recommends vaccines to the British schedule. He very likely also sits on the British government’s mysterious Scientific Advisory Group for Emergencies.  Age of Autism has been higlighting the manifold and apparently contradictory roles of Prof Pollard for more than four years. In 2014 as recently appointed chair of the JCVI he recommended Bexsero meningitis B vaccine of which he was lead developer to the UK infant schedule, leading to a sudden leap in its commercial prospects. Even the package insert discloses serious dangers for Bexsero including a 3 in 1000 risk of Kawasaki Disease for an infant having three doses. 

While Pollard and likely the British government's plans rush forward many scientists have questioned either the wisdom of the COVID-19 vaccine or how fast one could be brought to the market. On the present time scale we will know nothing of the long term effects. Tests will be carried on healthy people 18-55 but rolled out for children, the sick and the elderly. It will be trialled against "a control injection" not genuine placebo, (in fact a Men ACWY vaccine). At present we do not even know if the disease itself results in long term immunity or any immunity against all the other mutations which are beginning to proliferate. Meanwhile, the OVG promotes discussion about whether vaccination should be made compulsory. Indeed, if it were it would be Prof Pollard's committee which would decide what every man, woman and child in the United Kingdom would receive, and would not be able to refuse.

This is Pollard’s most recent disclosure in the JCVI minutes:

Professor Pollard receives no personal payments from the manufacturers of vaccinesHe is Director of the Oxford Vaccine Group in the Department of Paediatrics, University of Oxford and has current research funding from the Bill and Melinda Gates Foundation, the National Institute for Health Research, the European Commission, Medical Research Council, Wellcome Trust, InnovateUK, Meningitis Research Foundation, and the Global Alliance for Vaccines and Immunisation. Hechairs the scientific advisory group on vaccines for the European Medicines Agency and is a memberof WHO’s SAGE.Other investigators in the Department conduct research funded by vaccine manufacturers and theDepartment has received unrestricted educational grant funding for a three-day course on paediatricinfectious disease from Gilead, and GSK in June 2019.

While it is inevitable that any scientist is going to be an enthusiast for is or her own research the long term indifference of the British government to traditional checks and balances is deeply concerning, and no less so at this difficult time. 

Recruitment begins for a clinical trial of a COVID-19 vaccine led by Andy Pollard

andrew pollard

Professor Andrew Pollard, Vice Master of St Cross College, is the Chief Investigator on a new study developing a possible vaccine for COVID-19. The 'ChAdOx1 nCoV-19' vaccine, as it is called, was developed by a team of University of Oxford researchers based on an adenovirus vaccine vector. A collaborative team from the Jenner Group and the Oxford Vaccine Group is now recruiting over 500 healthy volunteers for clinical trials of the vaccine. While applications for volunteers have closed, those interested in volunteering for future COVID-19 studies can register interest here.

Pollard is one of a team of academics, which includes himself, Professor Sarah Gilbert, Professor Teresa Lambe, Dr Sandy Douglas and Professor Adrian Hill, who began the project on Friday 10 January 2020. Pollard said, ‘Starting the clinical trials is the first step in the efforts to find out whether the new vaccine being developed at Oxford University works and could safely play a central role in controlling the pandemic coronavirus that is sweeping the globe.’

You can read more about the study here.

Riley Lewis

7 April 2020

J&J Gets $450 Million Coronavirus Vaccine Contract from Trump Administration

Vaccine piperTylenol. Risperdal. Baby powder. Trusted brands. Huge lawsuits.  And now the vaccine that may be mandated for you to access society soon...  Johnson & Johnson has been tapped by the US Government to create a Coronavirus vaccine. Imaging the market - and no product liability.

From DRUGWATCH:  Johnson & Johnson is the world’s largest health care company. It is also the highest paid drug company in the world. J&J remains at the top of the Big Pharma list of powerful corporations. It is well known for consumer products like Band-Aids, Johnson’s Baby Powder and Tylenol. Its drugs, devices and products have led to scandals and lawsuits.  A Huffington Post investigation called J&J “America’s most admired lawbreaker.”

HUFFINGTON POST: Over the course of 20 years, Johnson & Johnson created a powerful drug, promoted it illegally to children and the elderly, covered up the side effects and made billions of dollars. This is the inside story.

And in current news:

The U.S. Just Signed A $450 Million Coronavirus Vaccine Contract With Johnson & Johnson

The Trump administration is spending nearly half a billion dollars on one company in the race to find a coronavirus vaccine.

That’s according to a $456 million order with Johnson & Johnson’s Pharmaceuticals arm Janssen, which specified a “new vaccine asset for 2019 Novel Coronavirus (COVID-19),” Forbes found. It’s the largest reported amount spent on a vaccine project to date, even though the pharma giant hasn’t yet started any clinical trials as other firms have.

The deal was signed with the Health and Human Services Office of the Assistant Secretary for Preparedness and Response (ASPR) on March 27, 2020. It followed another order, made as part of the same contract with Janssen, for $150 million on March 20, 2020, for a “new antiviral” for COVID-19.

A spokesperson from Johnson & Johnson didn’t provide any more details on the specific order, but confirmed the $456 million award related to a collaboration with ASPR’s Biomedical Advanced Research and Development Authority (BARDA), as announced in February. That work was built on previous contracts for developing countermeasures for other influenzas. The value of the coronavirus-specific work hadn’t previously been revealed and is the largest known contract for a coronavirus vaccine to date.

Whatever happened to Paul Offit’s 10,000 vaccines?

image from www.rescuepost.comThese are Paul Offit’s comments posted on his Facebook page earlier this week: an acknowledgment that vaccines are dangerous. Whatever happened to ten thousand vaccines are safe for an infant?

Which will do more harm, the virus or the fear of the virus?

Why are we so scared of the novel coronavirus, COVID-19? People are usually scared of viruses for three reasons:
One: the virus causes gruesome, disfiguring, permanent symptoms. Smallpox, for example, not only caused life-long facial scarring, it also was a frequent cause of blindness in those who survived.
Two: the virus has a predilection for children. Polio paralyzed tens of thousands of young children every year until a vaccine finally eliminated the disease from the United States.
Three: the virus is likely to kill you. Rabies kills virtually 100 percent of people who develop symptoms after a bite from a rabid animal.
The novel coronavirus currently circulating in the United States—the one that has caused us to shut down schools, restaurants, sporting events, and virtually every aspect of our culture—falls into none of these categories. Nonetheless, people are scared. Really scared. The reason is they think that if they catch COVID-19, they have a high likelihood of dying from the disease. Most public health officials have done little to lessen this fear, arguing that people are ten times more likely to die from this novel coronavirus than from influenza. Unfortunately, these officials haven’t made clear the difference between relative risk and absolute risk. Although people are more likely to die from COVID-19 than from influenza, they are far more likely to catch influenza. Therefore, they are far more likely to die from influenza.
According to the Centers for Disease Control and Prevention, as of March 7, 2020, 36 million to 51 million people have suffered from influenza, 370,000 to 670,000 have been hospitalized, and 22,000 to 55,000 have died from the disease. To put these numbers in perspective, let’s look at countries that have dealt with COVID-19.

China, where COVID-19 originated, has reported roughly 3,000 deaths. The population of China is about 1.4 billion, three times greater than ours. If we suffer an equivalent proportion of deaths, then 1,000 Americans will die from COVID-19, one-twentieth to one-fiftieth of the number who have died from influenza.
Italy has reported roughly 2,000 deaths from COVID-19 and, as a result, has shut down the country; only grocery stores and pharmacies remain open. Italy has a population of 60 million, about one-fifth of the U.S. population. If we suffer an equivalent proportion of deaths, then 10,000 Americans will die of COVID-19, about one-half to one-fifth of the number of deaths from influenza.
Not everyone, however, is at equal risk of dying. The virus primarily kills the elderly and those suffering from chronic diseases, which explains the situation in Italy, where 25 percent of its population is more than 65 years of age; in the U.S. it’s 16 percent. Wouldn’t it make more sense, then, to ask people who are elderly and infirm to stay away from crowds, thus lessening their chances of contracting the disease. Also, to ask people who are sick with respiratory symptoms to stay home. Focus on common sense things like washing hands several times a day and standing clear of people who are coughing or sneezing. The federal government can also help by making it easier for businesses to allow people who are ill to stay home.
In 2009-2010, the world suffered an influenza pandemic caused by swine flu; about 203,000 people were killed by the virus; 12,000 in the United States. The novel coronavirus has killed about 6,000 people to date; 62 in the United States. It doesn’t make sense to shut down our entire way of life to try and stop a virus that is unlikely to harm healthy people and will be far less devastating than the influenza epidemics that we experience every winter and the influenza pandemic we experienced ten years ago. Let’s take common sense measures to stop the spread. The precautionary principle dictates caution to prevent harm. But the precautionary principle also dictates that you don’t cause harm in the name of preventing harm. It will take years to recover from the draconian measures that we are currently instituting.


Six-in-One Vaccine Vaccine from Merck & Sanofi Raises Red Flag

Sesame street 6Note: Excerpted from Children's Health Defense. I took a look at the package insert for this new 6 in 1 vaccine called Vaxelis.  Take a look at the contraindications for yourself.

Severe allergic reaction (e.g., anaphylaxis) to a previous dose of VAXELIS, any ingredient of VAXELIS, or any other diphtheria toxoid, tetanus toxoid, pertussis-containing vaccine, inactivated poliovirus vaccine, hepatitis B vaccine, or Haemophilus influenzae type b vaccine.(4.1) •Encephalopathy within 7 days of a previous pertussis-containing vaccine with no other identifiable cause. (4.2)•Progressive neurologic disorder until a treatment regimen has been established and the condition has stabilized.

How does one KNOW if one is going to have a severe allergic reaction if there is no test for who may be susceptible? This vaccine contains both yeast and soy.  And Each 0.5 mL dose contains 319 mcg aluminum from aluminum salts used as adjuvants.   There's an admission that pertussis vaccines can cause encephalopathy. "With no other identifiable cause,"? What doctor has ever said, "Oh! That's a vaccine injury, Mom."  In fact, world "renowned" doctors testify in vaccine court on behalf of the pharma companies that this type of injury is so rare as to be negligible.  Would autism be considered a progressive neurological disorder and what would doctors call a treatment regimen: early intervention??



A Six-in-One Vaccine Associated with Sudden Infant Death

The childhood vaccine schedule in the U.S. features numerous combination vaccines—formulations that bundle multiple antigens for multiple diseases into one injection. Examples of combination vaccines currently given to American children include Merck’s four-component ProQuad vaccine against measles, mumps, rubella and varicella and Sanofi’s five-in-one Pentacel vaccine against diphtheria, tetanus, pertussis, polio and Haemophilus influenzae type b.
The inclusion of Recombivax raises an instant red flag, given that it contains a problematic proprietary aluminum adjuvant possibly linked to serious autoimmune conditions.

Now, the U.S. is preparing to up the combination vaccine ante still further. At the close of 2018, the FDA approved the nation’s first six-in-one (hexavalent) vaccine—a Merck and Sanofi joint effort called Vaxelis intended for infants at ages two, four and six months. Like hexavalent vaccines given to infants in other countries, Vaxelis combines the five components featured in Pentacel along with Merck’s genetically engineered Recombivax vaccine against hepatitis B (HepB).

The inclusion of Recombivax raises an instant red flag, given that it contains a problematic proprietary aluminum adjuvant possibly linked to serious autoimmune conditions. In fact, when a Merck cyberattack in the summer of 2017 temporarily forced Recombivax out of the U.S. pediatric market and American children received GlaxoSmithKline’s HepB vaccine instead, annual reports of HepB vaccine-related deaths to the Vaccine Adverse Event Reporting System (VAERS) dropped by roughly 75% and injury reports halved.    Read more at Children's Health Defense here.

Why We Cannot Believe Brian Deer About Andrew Wakefield

House of Commonsby John Stone

This is part of evidence I presented to  the United Kingdom House of Commons Science and Technology Committee Inquiry into Research Integrity in 2017. It was never published by the Committee but after much argument they were forced to amend their discussion document, known as POSTnote 544, so that it did not directly allege that Andrew Wakefield committed fraud by only attributing the claim to British Medical Journal. It is dismaying that we are still having to rebut so many false claims so many years after the events. The publication of Brian Deer's book is now only a couple of months away, but it has also been sad to see distinguished Danish scientist, Peter Gøtzsche, recycling these allegations in a book of his own. Prof Gøtzsche is in many respects a hero because of his stand against SSRI antidepressants (which are also implicated in autism) and on the safety HPV vaccines, but when he sides with Deer on the subject of Andrew Wakefield we wonder whether he has on this occasion done due diligence.

Brian deer updated
Brian Deer

An Extract From Evidence to House of Commons Science and Technology Inquiry into Research Integrity 2017 by John Stone on Behalf of Age of Autism

I am grateful to the committee for the invitation to submit evidence on behalf of Age of Autism. This evidence has been shaped by statements made in the Committee’s prior publication POSTnote 544 singling out the Wakefield “Lancet paper” as an example of fraud, and particularly in relation to the defence of a public health programme and policy [1]. If these statements had not been made I might have presented somewhat different evidence, but in the circumstances it is necessary to address these claims and their underlying assumptions.  It becomes particularly relevant in the light the latest campaign, led by Times Newspapers, to further discredit Andrew Wakefield.

This submission is not motivated by indifference to the control of infectious disease. What I am saying is that even though the control of disease is important it is not a good enough reason to stand the rules of research integrity or public discussion on their head. For this reason I have things to say not only about the Wakefield paper but the problematic nature of vaccine science, and also the general exclusion of the subject from contemporary mainstream public debate. Even the reasons for going to war at times of national peril are debated, but here it is as if everything has been conceded in advance to an industry and its public advocates. In these circumstances reasonable comment is driven to the margins with unreasonable, even to the extent of being buried by search engines such as google.

It is also problematic that virtually every public defence of the vaccine programme begins with an attack on the integrity of Dr Andrew Wakefield, as if the public humiliation of one man could provide scientific justification in perpetuity for an entire class of products. Wakefield has been globally transformed into the Emmanuel Goldstein of public health (to reference Orwell’s 1984) but we should not mistake that this is actually occurring at the level of propaganda and not of scientific (or historic) fact: indeed when people cite Wakefield as an example few have the remotest idea what body of facts they are citing, and this has reduced to zero the quality of informed public discussion. Meanwhile Wakefield’s fate serves as a warning to anyone else who might professionally step out of line. In this context I pose the question in what other field of human activity would this means of controlling public discussion and opinion be considered politically tolerable? I also pose the question how we can possibly know the vaccine programme is safe if we control opinion in this way?

Continue reading "Why We Cannot Believe Brian Deer About Andrew Wakefield" »

Neonatal Nurse on Vaccines: We are Destroying an Entire Generation of Children

8AE8EB37-B328-437E-A94F-4215B3E7C640By Brian Shilhavy
Editor, Health Impact News

Michelle Rowton is neonatal nurse practioner, specializing in the care of children ages 2 years old and younger. She has worked for over 17 years working in NICU, with pre-mature and sick babies.

Michelle Rowton does not herself give vaccines to babies.

She recently sat down and conducted an interview with Polly Tommey during the VAXXED II film bus tour.

Michelle relates that in her undergraduate training to prepare her to be a nurse, that the only thing she was taught about vaccines was how to give the injections.

When she was in graduate school studying for her master’s degree to become a neonatal nurse practioner, she says she was taught “coercive rhetoric” to get the parents to agree with vaccines.

Michelle discusses her early years of working in the NICU with premature babies, and the negative effects vaccines would have on these babies.

Polly then relates how vaccine apologists in the medical field will rationalize giving vaccines to young babies by stating that they have seen many deaths related to vaccine-preventable deaths among unvaccinated babies.

So she asks Michelle how many of these deaths by diseases that are allegedly prevented through vaccination that she has seen during all her years as a nurse, and she replies, “zero.”

They’re lying. Especially when they bring up chicken pox. I’m like, what nation were you in when that happened? Because it hasn’t happened here.

Michelle also works as a Functional Medical Nurse practioner in the field for the past 7 years, where her focus is working with babies out in the field.

I moved out of the hospital and into the clinic, because I got to the point where I thought, this is the same thing over and over again. Yeah, I’m really good at putting in central lines, and putting in chest tubes, and saving these critical babies.

When they get to the convalescence stage, it is terrible what we’re doing, and everybody’s doing the same thing.

I can have more effect out in the community, in having these babies from birth until two – no antibiotics, no ear infections, no medications, setting them up for life to have a far less chance of autoimmune disease, chronic disease – all of that kind of stuff.

That’s what I want to do now.

Michelle has three children of her own, all unvaccinated, and never been on antibiotics.  READ MORE HERE.

WHO’s malaria vaccine study represents a “serious breach of international ethical standards”

'Are_you_a_mosquito_breeder'_-_NARA_-_513877Thank to The Highwire for posting this report.  If there has been a serious breach in ethical standards on a program to eradicate malaria, a disease man has been fighting forever, can you imagine what might happen in order to get a Coronavirus vaccine out quickly to the masses?  Our Dan Olmsted broke the story of the dangerous malaria drug Lariam with his writing partner Mark Benjamin almost two decades ago. As always, we miss his presence and his take on this current situation.

By Peter Doshi, associate editor THE BMJ

Experts are troubled by the apparent lack of informed consent in a large, cluster randomised study of the malaria vaccine. Peter Doshi reports

A large scale malaria vaccine study led by the World Health Organization has been criticised by a leading bioethicist for committing a “serious breach” of international ethical standards. The cluster randomised study in Africa is already under way in Malawi, Ghana, and Kenya, where 720 000 children will receive the RTS,S vaccine, known as Mosquirix, over the next two years.123

Mosquirix, the world’s first licensed malaria vaccine, was positively reviewed by the European Medicines Agency, but its use is being limited to pilot implementation, in part to evaluate outstanding safety concerns that emerged from previous clinical trials.3 These were a rate of meningitis in those receiving Mosquirix 10 times that of those who did not, increased cerebral malaria cases, and a doubling in the risk of death (from any cause) in girls.2


Advisory Committee on Immunization Practices (ACIP) Meeting 2/26 and 2/27

Approved-stampAdvisory Committee on Immunization Practices (ACIP)
Centers for Disease Control and Prevention (CDC), Atlanta, GA
February 26, 8:00 am – 5:00 pm
February 27, 8:00 am – 2:30 pm

Agenda includes Ebola and Flu vaccine. One would assume Coronavirus will be featured.
Agenda here.

Webcast instructions here.

Listen via phone:

Toll Free: 1-877-925-7916
Passcode: 4080878459

Any member of the public can submit a written public comment to ACIP. Written comments must be received on or before February 28, 2020.  You may submit comments for the February 2020 ACIP meeting, identified by Docket No. CDC-2020-0002, using the Federal eRulemaking Portalexternal icon. Follow the instructions for submitting comments. All submissions received must include the agency name and Docket Number.

All relevant comments received will be posted without change to http://regulations.govexternal icon, including any personal information provided. For access to the docket or to read background documents or comments received, go to http://www.regulations.govexternal icon. Comments submitted by 72 hours before the meeting will be made available to ACIP members in advance of the meeting. Comments will be accepted up to 48 hours following the end of the ACIP meeting


The Jig Is Up: Dr. Richard Moskowitz on Vaccine Mandates

Richard Moskowitz MDNote: I have had the pleasure of meeting Dr. Moskowitz. He personifies the dignified doctor of "yore" when patients came first.  He is the author of Vaccines: A Vaccines Richard MoskowitzReappraisal from Skyhorse Publishing.

I invite you to share this article he has written to address the current crushing slate of vaccine mandates. Here in my state of Connecticut, we are waiting for a vote on HB 5044 which will remove our religious vaccination exemption.  Kim


By Richard Moskowitz, M. D.

As a GP with more than 50 years' experience in treating children and their families, I feel it my duty to speak out against the new vaccine mandates, for three main reasons.  The first is that there is no emergency to justify vaccinating children against their parents' wishes, let alone keeping them out of school if they refuse. 

The second is that the research cited to prove that vaccines are safe and effective falls far short of the rigorous standards that valid medical science must follow.  The third is that the Nuremberg Code and the Helsinki Declaration, both of which we helped write and still profess to abide by, explicitly forbid any medical procedure, treatment, or experiment undertaken without the fully-informed consent of the recipient.

There is no emergency.

I'll take the easy one first.  The public hysteria that has led a number of states to declare an emergency arose largely in response to measles outbreaks in 2016 and 2019. While a little larger than in the recent past, these were still quite small, localized, and in most respects similar to those recorded in every year since the vaccine was introduced, numbering just over 1000 cases in 2019, compared to a few hundred in the years since 2000, when the CDC prematurely declared the disease eliminated from the United States,1 and anywhere from 400,000-800,000 cases annually in the pre-vaccine era.2  If the CDC would just admit that they were a little hasty, and that such outbreaks are bound to occur, they could still claim a historic victory over this formerly ubiquitous disease. It's also worth remembering that virtually everyone of my generation came down with measles in grade school and recovered without complications; nobody thought it an emergency back then, so there was no urgent need for a vaccine in the first place.

In any case, the hysteria behind the present campaign to eliminate all religious and philosophical exemptions is utterly disproportionate to the facts on the ground. My own state of Massachusetts has seen 0-3 measles cases per year for the last 5 years, and only 44 cases in the past decade,3 with 97% of our kindergartners and 99% of our seventh-graders already vaccinated with the MMR,4 well above the official target of 95% for the stricter new mandate that it has in mind. 

The alleged emergency rests on two assumptions so widely regarded as self-evident that they are rarely challenged:

1) that these measles outbreaks are spread mainly by the unvaccinated, and

2) that vaccines are so effective that only the unvaccinated are still susceptible and thus capable of transmitting the disease to others.

Unfortunately, there is ample scientific evidence that exactly the opposite is true.  Although public health officials rarely admit it, the vast majority of the cases of measles, mumps, chicken pox, whooping cough, and influenza in both past and recent outbreaks, typically from 75-95%, have been in vaccinated individuals;5 in the case of mumps, the figure is typically 95-100%.6   So even if everyone was vaccinated, and all non-medical exemptions eliminated, as the new laws require, similar outbreaks are virtually certain to continue. 

We also know that individuals receiving the "live" vaccines (measles, mumps, rubella, chickenpox, rotavirus, and oral polio) "shed" them for weeks afterward, and are contagious to family members, friends, and close contacts.7   As for "non-living" vaccines, recent studies show that current outbreaks of whooping cough are likewise being spread mainly by vaccinated individuals, through the development of vaccine-resistant strains,8 while analogous mutations have been documented in the case of HiB, pneumococcus, IPV, HPV, and other non-living vaccines as well.9   In short, the push to vaccinate everybody, and the bullying that typically accompanies it, actually help to propagate the diseases that the vaccines were meant to eradicate.

The only scary feature of the 2019 outbreaks is that a large number of those infected have been shown to bear the genotype of the vaccine virus, rather than the wild type,10 so that for the first time a significant proportion of the cases are unvaccinated, providing still more convincing proof that the vaccine is spreading the disease, because the disease itself has mutated in response to it, an ominous sign for the future.

Claims that vaccines are safe and effective are deceptive.

Continue reading "The Jig Is Up: Dr. Richard Moskowitz on Vaccine Mandates" »

European Protest for Medical Freedom – Munich 2020

German american flagsEuropean Forum for Vaccine Vigilance is organizing a protest over the encroachment of the pharmaceutical industry on our civil rights and pyhysical integrity in Munich on 21 March, to be addressed by Robert F Kennedy Jr, Vera Sharav (holocaust survivor and founder of Alliance for Human Research Protection), Del Bigtree, Sherry Tenpenny, Senta Depuydt, Kris Gaublomme (EFVV), Jusyna Socha (Stop Nop Poland), and the will be presentation by CORVELVA regarding their investigation of vaccine vials. Details are available from the EFVV website.  The protest will start (and end) in Odeonsplatz at 11.30 am and close at 5pm. There will be a stage there and during the day we'll also march in the city center.

Germany is the latest European country to introduce mandatory vaccinations (measles only, but they don't provide the single vaccine) and the German associations are now asking the intervention of the Constitutional Court to try and stop the law, that will otherwise start its effects from March 1st.

It's the only Country that extended the obligation to all the categories working with children: healthcare pratictioners, doctors, nurses, teachers...


We’ve finally had enough of an almighty pharmaceutical industry censoring our internet, controlling our media, our courts and our governments.

Mandatory vaccination is a violation of our physical integrity, of our freedoms guaranteed to us by the Charter the UN and the Universal Declaration of Human Rights, and is limiting our access to education, employment and the free circulation of citizens.

The global agenda of mandatory vaccination is marching fast. After Italy in 2017 and France in 2018, many other countries are following suit. The latest country to fall is Germany in 2020. These mandates will soon be extended to adults, pregnant women and the elderly.

The Network for Vaccine Choice Germany, in collaboration with the European Forum for Vaccine Vigilance is organizing a massive protest to show the world that we are here, more determined than ever.

This is not the time to hesitate. It is high time to act.

Join us in Munich on March 21st, 2020. It is easy to register on the EFVV web site: just enter your details (name, surname, country, email for updates, intended travel plans).

Let's show Europe how many we are. Large numbers will affirm our connectedness, our commitment and our strength.