Vaccine Safety

Liquor Then Beer Never Fear, Moderna Then Pfizer WHO Says To Be Wiser

Bad Food combo"A little bit of a dangerous trend." WHOSpeak for "We' have no idea the health and safety consequences, but we are not allowed to alarm anyone from continuing to get a dose, any dose, for God's sake please take your dose."

GENEVA (Reuters) - The World Health Organization’s chief scientist on Monday advised against people mixing and matching COVID-19 vaccines from different manufacturers, calling it a “dangerous trend” since more data is needed about the health impact.

“It’s a little bit of a dangerous trend here,” Soumya Swaminathan told an online briefing. “It will be a chaotic situation in countries if citizens start deciding when and who will be taking a second, a third and a fourth dose.”

Swaminathan called mixing a “data-free zone” on Monday but the WHO clarified on Tuesday that some data was av

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Bad, bad superbad combos

ailable and more was expected.

Its Strategic Advisory Group of Experts on vaccines in June said the Pfizer vaccine could be used as a second dose after an  initial dose of AstraZeneca, if the latter is not available.

The results of a further clinical trial led by the University of Oxford that will look at mixing AstraZeneca and Pfizer as well as Moderna and Novovax vaccines is underway.

“Data from mix and match studies of different vaccines are awaited - immunogenicity and safety both need to be evaluated,” the WHO said in emailed comments.

It should be public health agencies who make decisions, based on available data, and not individuals, the WHO added.

Reporting by Emma Farge and John Revill; Editing by Hugh Lawson and Raissa Kasolowsky


Covid-19 Jab Op-Ed

AofA Op EdBy Dr. William H. Gaunt, NMD

The Covid-19 vaccines have considerably more negative effects than most people realize. The question is how frequent and how bad are they? VAERS stands for Vaccine Adverse Events Reporting System. A 2011 report by Harvard Pilgrim Health Care, Inc. for the U.S. Department of Health and Human Services (HHS) said that less than 1% of all vaccine adverse events are reported to the government through VAERS. Think about that. This is an important factor: Only a tiny fraction of vaccine deaths and injuries get reported to the government by this system.

Another interesting bit of recent news: OSHA (The Occupational Safety and Health Administration) has given employers a break by saying that they don’t have to report Covid-19 vaccine adverse events if they simply “recommend” but don’t “require” these vaccines. This will result in even less reporting.

The Covid-19 vaccines began in December 2020. No vaccines have ever been more heavily promoted and they are being given free of charge for most people. Millions of people are getting them. The government is paying for these vaccines.

The VAERS data through June 25, 2021 showed 6,985 reports of deaths and 34,065 reports of serious injuries following Covid-19 vaccines. This includes 576 deaths of unborn babies. These reports come from the CDC but are not widely reported. We need to do some math to get an estimate of how many actual deaths and injuries have occurred.

Let’s first be very generous and assume that 5% of deaths and injuries caused by Covid-19 vaccines are being reported through VAERS. The math goes like this: 20 times 6,985 equals 139,700 deaths and 20 times 34,065 equals 681,300 injuries. This is almost certainly an underestimate.

Let’s try a more realistic estimate. If 2% of deaths and injuries are being reported through VAERS, the math goes like this: 50 times 6,985 equals 349,250 deaths and 50 times 34065 equals 1,703,250 injuries. These numbers seem impossible even to me but may be close to the actual carnage.

Continue reading "Covid-19 Jab Op-Ed" »


Levi Quackenboss’ Gentle Approach to Helping Parents Learn About the CV For Their Kids

Spoonful of sugarUpdate: Facebook 30 day banned at least one person who posted this info yesterday.

BOSS not bush! I do it every time!! 

Levi Quackenboss  is known for his acerbic wit and sharp, educational blog posts. But below you'll see his softer side, as he takes the dump truck full of sugar approach to help a friend learn facts about the Covid vaccines and children. Parents don't get this information from their pediatricians, their news sources or most of their equally unaware friends.  We are so entrenched in the world of medical rights and vaccine injury and disability, that we often forget that the MAJORITY of those around us are not only brand new to the concepts, but have been actively educated to believe anything but what we share. There is a time to use lemon, and a time to use honey. And a hive full of facts. Levi is a Queen (King?) Bee for this work.

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Hi, friend. I noticed your post the other day-- the one about making sure your child wears a mask until they can be vaccinated this fall--when the Pfizer COVID vaccine will be awarded emergency authorization for use in kids under 12. You know my stance on this specific issue, and of course, I know yours, but I hope this note finds you open and willing to receive some information before you finalize that monumental decision for your child. 

Mainstream media haven't reported much on the children and young adults harmed by these vaccines, so I understand that their stories may not have made it onto your radar. I'd like to tell you about a couple of them.

The first is a 12-year-old girl named Maddie de Garay. Maddie's parents allowed her and her two brothers to enroll in the Pfizer trial where 1,100 kids aged 12-15 received the real Pfizer COVID vaccine. One brother received a saline placebo. The other received the real vaccine and quickly became infected with a severe case of COVID, serious enough to cause him to miss many weeks of school. But Maddie's experience was different. Her body lost the ability to digest food and she also lost the ability to walk. While this happened back on January 20, 2021, she still uses a wheelchair and still has a feeding tube today. Her medical team declared her new health status to be a mental issue and suggested she be committed to a psychiatric hospital. Pfizer did not stop their trial and has not publicized this child's injuries. You can watch Maddie's mother, an engineer, testify at a US Senator's press conference here: https://www.youtube.com/watch?v=zp_zNSEW1wc&t=355s

The next child is Jacob Clynick. Jacob was 13 years old when he received the second dose of the Pfizer vaccine on June 13, 2021. He died three days later of an enlarged heart and myocarditis, which is inflammation of the inner heart wall. The CDC says it's "investigating" Jacob's death. You can read about Jacob here: https://www.rt.com/usa/527177-twitter-vaccine-boy-died-heart/

Continue reading "Levi Quackenboss’ Gentle Approach to Helping Parents Learn About the CV For Their Kids" »


NYT Commenters Triggered By Mere Suggestion

C7DD5335-F30C-4002-BBA4-52075844F883A young man, only 20 years of age, died during a surgery to repair his pitching arm and news outlets everywhere reported it. I saw The New York Times' article on Facebook, and read with grim curiosity. When I read that he had suffered a blood clot, my curiosity grew grimmer. Just last week, the CDC cancelled an emergency meeting to talk about heart problems in young adults who are Co-Vaxxed. The J&J brand was temporarily halted for suspected blood clots. The Astra-Zeneca brand has reports of blood clots. So, having this basic information in my head, I bravely commented with respect and without grandstanding, to ask if the young man had been Co-vaxxed recently. He's a ball player at a University. It stands to reason that he was. But oh how I triggered commenters! See the horse in the photo, kids? That's Roy Rogers' trusty steed who was named Trigger, I thought an actual gun trigger would be untoward. And social media is less likely to shut down a post with a photo of a horsey.

Take a look at the comments in response to my comment on Facebook below. NYT vaxolytes can't even handle the mere mention of a side effect. They immediately pulled out the old "what's YOUR degree in, lady?"  "STFU!"  How dare someone who is not an epidemiologist comment on side effects!  I thought that was an interesting comment, likely inserted by a pharma troll. Lots of syllables in epidemiology for the average reader. You can hear the cognitive dissonance rattling around in their brains.  Boys, boys, boys, I have a PhD in vaccine injury. 

This is what we're up against and what has been bred into people for now two decades. Vaccines CAN NOT be questioned even when the likelihood of a connection is sky high.

 

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Eric Clapton Video from Oracle Films




You might want to take video of this exclusive on your phone, so when YouTube takes it down, you have proof it existed. Eric Clapton is going way out on a limb to speak out about what happened to him when he took the jab. It almost cost him his lifelong career. I saw many people on Twitter immediately writing him off - after decades of loving his music from the days of Cream to today. It's amazing that as soon as someone speaks the truth about their vaxperience, the "We are the world, we are the children" community turns on him like a rabid dog. Fans drop him. We know better. Welcome, Slowhand. We're sorry you are here.



Trust Has Been Long Gone

Trust and safetyAs the news comes out about Dr. Anthony Fauci's email after email contradicting the how and why of the pandemic, many of us just shake our heads with a weary sigh. Tucker Carlson: Uncovered Emails Show Fauci Supported ‘Grotesque’ Experiments at Wuhan Lab  Fauci presided over the catastrophic rise of autism - and did nothing but hem and haw and tell us what is wasn't - vaccines. Vaccines. Vaccines. Vaccines. We're often accused of being too vaccine-centric. It has cost us dearly. Sponsors. Gone. Donors. Sparse but much loved. Google. Shut us down. But when we think of what vaccines have cost our families, it's a small price to pay.  Here, Jeremy Hammond wrote in March about yet another scandal involving WHO, children and vaccines - without informed consent. Malaria has a close to tie to Age of Autism. Our founder Dan Olmsted broke a huge story about Lariam, a drug for Malaria, with his UPI writing partner Mark Benjamin. Army eyes malaria drug in Bragg killings.

You'd think in today's world, a story about WHO potentially harming African children would be splashed everywhere with indignation. You'd think.

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WHO Experimenting on African Children without Informed Consent

The World Health Organization (WHO), a pair of articles recently published in The BMJ have revealed, is sponsoring an experimental study of a controversial malaria vaccine among African children without obtaining informed consent from parents.

Data from prior clinical trials of the vaccine, manufactured by the British multinational pharmaceutical corporation GlaxoSmithKline (GSK), have shown it to be associated with an increased risk of clinical malaria after four years, a tenfold increased risk of meningitis, an increased risk of cerebral malaria (in which the parasitic organisms block the flow of blood to the brain, causing swelling and potential brain damage), and an increased risk of death that was disproportionately higher for female children.  Read more at JeremyHammond.com.


Guitar Legend Eric Clapton Describes His Cov Ax Reaction



Eric Clapton needs no introduction. He may need to learn our secret handshake. "...the reactions were disastrous, my hands and feet were either frozen, numb or burning, and pretty much useless for two weeks, I feared I would never play again,"

"I never should have gone near the needle."

I am an old timer, I have survived, with great help, addiction and alcoholism, and stand now in the greatest dilemma of my life…

I have inwardly stood against our ‘elected leaders’ since brexit, intuitively doubting their integrity and character…

With the arrival of C-19 I hoped that C Henegan, S Gupta and Jay B would lead the way, but when imperial college stepped up with their jailers key, I knew we were in deep trouble…

I am a man of faith, albeit abstract, and what I felt and saw unfold in March ‘20 began to lead me away from govt rhetoric and the devotion of the general public to the PM and his cronies…

I looked for heroes in the house, and found C Walker, Desmond Swayne, and in unfortunate retirement, Lord Sumption…

On YouTube I found Hugotalks and Talk Radio… that was all….

Then I was directed to Van M, that’s when I found my voice, and even though I was singing his words, they echoed in my heart…

I recorded “stand and deliver” in 2020, and was immediately regaled with contempt and scorn…

In February this year, before I learned about the nature of the vaccines, (and being 76 with emphysema) I was in the avant garde. I took the first jab of AZ and straight away had severe reactions which lasted ten days, I recovered eventually and was told it would be twelve weeks before the second one…

About six weeks later I was offered and took the second AZ shot, but with a little more knowledge of the dangers. Needless to say the reactions were disastrous, my hands and feet were either frozen, numb or burning, and pretty much useless for two weeks, I feared I would never play again, (I suffer with peripheral neuropathy and should never have gone near the needle.) But the propaganda said the vaccine was safe for everyone….

Then I met a member of this group, who counselled me to be careful and to have a look at what goes on with you guys…

I felt like a veil had been lifted, that I was no longer alone, that it was okay, in fact essential, to hold on to my intuition and follow my heart…

I continue to tread the path of passive rebellion and try to tow the line in order to be able to actively love my family, but it’s hard to bite my tongue with what I now know…

I’ve recorded and will post here another song by Van called “The Rebels” it’s not aggressive or provocative, it just asks;

“Where have all the rebels gone?

Hiding behind their computer screens

Where’s the spirit, where is the soul

Where have all the rebels gone”

I’ve been a rebel all my life, against tyranny and arrogant authority, which is what we have now, but I also crave fellowship, compassion and love, and that I find here…

I believe with these things we can prevail

EC”


Weasel Words for Parents To Be

Weasel wordsI  looked up " covid vaccine safe for pregnant women" and found this statement as the top hit.

If you are pregnant, you may choose to be vaccinated when it’s available to you. There is currently no evidence that antibodies formed from COVID-19 vaccination cause any problem with pregnancy, including the development of the placenta.

Read it carefully, as if you have more than a second grade education. Smell the Swiss cheese and tell us what hidey holes for reality you see. We in the autism biomed community have seen this sort of "answer" over and over, about treatments like the gluten free diet and yes, vaccine injury. I've always been fond of analogies to make a point crystal clear. When Europeans could not see over the horizon, they knew beyond a shadow of a doubt that the world was flat. No one had every studied otherwise, and therefore no one could say it was not. Therefore, it was indeed as flat as a pancake. Until someone circumnavigated the globe.  David Kirby wrote Evidence of Harm because Lyn Redwood did something no researcher, CDC professional or pharma scientist bothered to do. She added up the individual bolus doses of mercury in the pediatric schedule and the rest is history. No one had bothered to look. But the harm was there.  I have two daughters about to come home from a day program for the intellectually disabled. The harm was there.

Here's an even simpler analogy. How many times has someone in your family hollered to you, "Maaaa!  We're out of ketchup," while standing there staring at one spot on one door shelf?"  The unopened ketchup is in the pantry.

And this from WebMD: More Signs COVID Shots Are Safe for Pregnant Women

April 20, 2021 -- As the U.S. races to vaccinate millions of people against the coronavirus, pregnant women face the extra challenge of not knowing whether the vaccines are safe for them or their unborn babies.

None of the recent COVID-19 vaccine trials, including those for Pfizer, Moderna, and Johnson & Johnson, enrolled pregnant or breastfeeding women because they consider them a high-risk group.

That was despite the Society for Maternal-Fetal Medicine and the American College of Obstetricians and Gynecologists asking that pregnant and breastfeeding women be included in trials. The FDA even included pregnant women in the COVID-19 vaccine emergency use authorization (EUA) due to their higher risk of having a more severe disease.

Despite that lack of clinical trial data, more and more smaller studies are suggesting that the vaccines are safe for both mother and child.

"Suggesting" safety. Is that enough for you?  It shouldn't be enough for anyone bringing a child into the world.

Look for the weasel words in everything you read.



 


Spike Protein 101: A Primer from Dr. Larry Palevsky

SARS-CoV-2_spikesThank you to Laura Hayes for transcribing a 12 minute primer on spike protein production and Covid vaccination by Dr. Larry Palevsky.  Dr. Palevsky brings up what can only be called horrifying questions, all unanswered because the powers that be have never asked. By design.  It's "easy" to say that what you have not looked for doesn't exist. Informally called, the blind eye.

By Laura Hayes

I have been wondering if those injected with the new "vaccines" are shedding that which might harm others with whom they come in contact, with the suspicion that they likely are. 
 
The video below addresses that, and I can't recommend strongly enough that everyone listen to it (only 12 minutes long).
 
Many of you know who Dr. Larry Palevsky is, and for those who don't, he is a NY pediatrician who has spoken out about the dangers of vaccines since the late 1990s, when a mother in his practice showed him that there was mercury in the vaccines he was administering to the children in his practice. That moment changed his life, and he began to do further research into vaccines. 
 
This clip that was sent to me today is a portion of an interview with him. I cannot find the full interview, but found this portion so compelling after listening to it 3 times that I decided to transcribe it. I hope you will first listen to it, then use the attached transcript to read any part you would like to reference again. Click on the second video at the link below (first is of a female, second is Dr. Palevsky). It is 12-minutes long, and worth listening to every minute of it.
 
 
For those of us who have children who have been harmed and/or killed by "routine" childhood vaccinations, Dr. Palevsky is a trusted and deeply appreciated rare gem among doctors. He speaks out often, and you can do a search of his name to listen to some of his public speeches, including his powerful testimony before the CT legislature in February, 2020:
 
I hope you will share this information with those you know, as the future fertility, health, longevity, and survival of humans may be hanging in the balance.

Transcript of Dr. Larry Palevsky:

When studies are done on injections that are thought to be vaccines, we sometimes need 7, 10, or even 15 years, to understand what the injection does to the body, and what it does to those around us.

And so, there’s automatically this assumption that when the authorities say these injections are safe, that we actually have adequate data and adequate observational data to understand whether or not these injections are safe. The bottom line is we don’t have enough data to understand their safety.

The other thing is that we are made to believe in the public eye that this is a vaccine against a viral infection. So, the entire world is thinking that this is a vaccine to protect us against SARS-COV2 infection. And when you have a vaccine that is supposed to be effective as a vaccine, you are supposed to have antibody immunity against the SARS-COV2 virus. And that has never been evaluated with these injections as to whether or not we have antibody immunity to a SARS-COV2 virus. Instead, what we have is the genetic information of what is believed to be a piece of the SARS-COV2 virus, and that piece is called the spike protein. And the technology that is being used is a technology to make this injection that has never been used in vaccine science or methodology before with any kind of success.

Continue reading "Spike Protein 101: A Primer from Dr. Larry Palevsky" »


Reports of Covid Jab Interrupting and Worsening Menstrual Cycles

StopThe article below is horrifying. Women like my three daughters will never have children, because of their severe autism. But they still have fully functional reproductive systems, and I'm not inclined to give them a potential lifetime of problems.  They have enough on their plates. Piled high. I'm sure the New York Times, Washington Post and other US daily rags (pun fully intended) will follow up to protect American women.

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Women say they are having heavier and more painful PERIODS since getting their COVID-19 vaccines - as several claim it has also messed up their monthly cycle

  • Dr. Kate Clancy, a University of Illinois associate professor, said that she'd heard people had experienced changes in their menstruation since getting vaccinated
  • Her tweet prompted other women to share changes to their own periods
  • Several reported that they were bleeding more heavily and for longer than they had before getting the vaccine 
  • A few said they began menstruating in the middle of their cycles, days or weeks before they were supposed to
  • Experts aren't sure why some women might see changes to their periods, and so far there is not enough data to know whether it is connected to the vaccine
  • A small study this year found that some participants saw changes to their menstruation after contracting the virus 

By Carly Stern For Dailymail.com

Several women say they have experienced heavier and more painful periods since getting the COVID-19 vaccine, with several also revealing that they have had breakthrough bleeding in the middle of a cycle after getting the shot.

Dr. Kate Clancy, an associate professor at the University of Illinois, tweeted in February that she'd been hearing talk of people who had experienced changes in their menstruation since getting one or two vaccine shots.

Her Twitter thread has prompted more women to share their menstrual concerns on Twitter, revealing their heavy flow, worsened cramps, and irregular timing — with one saying she spent 16 days bleeding after getting the Johnson & Johnson shot.  Read more including the COMMENTS here.


The Cult Mindset that Injury is Honorable

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Tinky Stinky. Dropsy. Wah Wah. Poo.


C vax injury is the new autism - hide it, deny it, make it seem normal, forget the real pain & suffering, tell folks to go about their biz, go back to the well of harm over & over. 

Read the screen shot below. Take note of grieving family members saying despite death, it's still important to take the C jab. "We trust the science” They did. They trusted the rushed experimental product that they were told was the solution. That is cult thinking.  It has been carefully cult-ivated for decades. We know this firsthand in the autism v injury community. It’s human nature to want to avoid buyers remorse at all costs. But when is enough too much?  People who’ve been jabbed and experienced  severe reactions saying they'd do it again, and some taking the second dose like martyrs and sacrificial lambs.

And there's no Noo Noo to tidy up. We're all on our own. Our true condolences to the family. 

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Dr. Meryl Nass: Latest vaccine flip-flop gives the vaccine game away

Cerebral-venous-sinus-thrombosis
https://virclinic.com/brain-hemorrhage/cerebral-venous-sinus-thrombosis/

The following is excerpted from Dr. Meryl Nass' blog with permission.

The Astra-Zeneca "cheap and easy to store" "workhorse" vaccine causes blood clots in general, and in particular clots in the venous sinuses of the brain, which have killed or wounded a number of people, especially women under 55.  

From StatNews:

Disorders caused by blood clots, including heart attacks, vein thromboses, and strokes, are common. But the types of clots that may be linked to the AstraZeneca vaccine are exceedingly rare. They have been marked by low levels of platelets — the blood cell fragments that normally cause clotting. 

The types of clots seen include cerebral venous sinus thrombosis, or CVST, a type of blood clot that occurs in the veins that drain blood from the brain, and a similar condition in the abdomen, known as splanchic vein thrombosis. The clots sometimes occur in combination with bleeding.

From the Washington Post:

The European Medicines Agency, the European Union’s regulator, said it is investigating at least 44 cases of the rare brain clots and at least 14 deaths among about 9.2 million vaccinations in 30 European countries...

As of March 29, Germany’s regulator has reported 31 cases of the unusual blood clots in 2.7 million people vaccinated with the AstraZeneca vaccine, nine of whom have died.

The J and J vaccine was also associated with blood clots in the clinical trial data presented to FDA.  Both vaccines use an adenovirus vector to deliver DS DNA that codes for spike protein, and human cellular machinery produces this protein, for an uncertain period of time in uncertain quantities. So blood clotting may be due to the adenovirus vector, or to the spike protein, or to something entirely different.

The mRNA vaccines use mRNA to code for the spike, also using cellular machinery to produce the spike protein.  The end result of all 4 vaccines is similar, and again, we do not know for how long the body makes this protein.

If the spike itself induces clotting, which is a reasonable hypothesis scientists have put forth, but is unproven, then all 4 vaccines would be thrombogenic (induce clotting). Dr. Patrick Whelan tried to warn the FDA about this possibility, but was ignored.  He wrote:

Meinhardt et al. (Nature Neuroscience 2020, in press) show that the spike protein in brain endothelial cells is associated with formation of microthrombi (clots), and like Magro et al. do not find viral RNA in brain endothelium. In other words, viral proteins appear to cause tissue damage without actively replicating virus.

Is it possible the spike protein itself causes the tissue damage associated with Covid-19? Nuovo et al (in press) have shown that in 13/13 brains from patients with fatal COVID-19, pseudovirions (spike, envelope, and membrane proteins) without viral RNA are present in the endothelia of cerebral microvessels.

This is frightening information, providing a strong hint of the spike protein's potential toxicity.  Read more HERE.


Sinovac Report

SinovacExcerpted from Epoch Times. Doesn't sound too different from what happens here in the USA. At least Europe and Canada have exercised an abundance of caution.  We hand out donuts and shame.

The Strange Sinovac Vaccine Phenomenon: Countries Report Increased Cases After Using Vaccine

By Eva Zhao

April 3, 2021 Updated: April 4, 2021

The Hong Kong government recently rolled out a large-scale vaccination plan against the CCP (Chinese Communist Party) virus, commonly known as COVID-19, but it’s been mired by frequent reports of serious adverse reactions. In just one month, 13 people died in Hong Kong after being inoculated, 11 of whom had been injected with the Sinovac vaccine, a Chinese domestically made vaccine.

The CCP has not reported a single case of serious side effects or death after it announced the administering of 100 million doses of the Sinovac vaccine in China on March 28.

But there are four strange phenomena of the Chinese Sinovac vaccine, analyzed as follows.

No Deaths Reported in China

Continue reading "Sinovac Report" »


Weasel Words From Oregon Health Authority


Pregnancy graphic
These are weasel words.  Who remembers, "Autism like symptoms" which meant, "Autism, but we can't say so and jeopardize the entire program?"  https://www.facebook.com/OregonHealthAuthority

Limited data = we don’t know.

Believe = maybe.

Unlikely = could be but we only want to scare you one way.

Specific risk = we don’t have clinical trial designed outcome reports so we can generalize for bow because these are experimental products.

Glad to see that  Oregon has adopted gender neutral language regarding pregnancy, as you can read. At least they have the social science down pat. We have no short term studies, let alone long term studies on Covid vaccines while pregnant. It's a complete crapshoot.

When I was pregnant in 1994, I remember walking as far away from the office microwave as I could.  When I was pregnant in 1996, I was aghast and terrified because I had had a Scotch and soda during my early pregnancy before I knew I was expecting Gianna.  In 2000 when I was pregnant, I should have smoked crack and eaten spoiled meat.

Wat a difference 20 years makes, eh?


No Means No Even with an Experimental Pandemic Jab

No does mean convince me Below is s an extremely important article from Children's Health Defense.  How many friends and family have told you they "had" to get the Covid jab to "keep their job."  The jabs are experimental, and recipients are clinical trial participants. Their use is for emergency purposes during a pandemic, they are not FDA approved. They were made faster and more "successfully" than any previous vaccines, even during the H1N1 flu pandemic, for which the vaccines were a catastrophe. No means no. We should not have to submit to a medical procedure to make another person feel "safer or better. Haste makes waste. Measure twice cut once. Vaccinate in haste, repent in leisure.

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Employees of the second-largest school district in the U.S. filed suit last week to prevent the district from mandating COVID-19 vaccines as a condition of employment.

California Educators for Medical Freedom, with assistance from the Health Freedom Defense Fund (HFDF), filed a federal lawsuit March 17 against the Los Angeles Unified School District (LAUSD).

In a press release, HFDF said LAUSD’s vaccine mandate violates federal law and basic human rights by requiring employees to take an experimental vaccine in order to remain employed.

All COVID vaccines available in the U.S. — Pfizer, Moderna and Johnson & Johnson — are approved under the U.S. Food and Drug Administration’s Emergency Use Authorization (EUA). By the FDA’s own definition, that makes the vaccines “experimental” until or unless the FDA licenses them.

School employees alleged in their complaint that the statute granting the FDA power to authorize a medical product for emergency use, 21 U.S.C. § Section 360bbb-3, requires that the person being administered the unapproved product be advised of the benefits and risks, and of his or her right to refuse the product.

The FDA issued a Fact Sheet for Health Care Providers and a Fact Sheet for Recipients and Caregivers for each of the three vaccines approved for emergency use. The fact sheets state, among other things, that a provider must communicate information to the recipient prior to administering the vaccine — including that the recipient has the option to accept or refuse the vaccine. Read more at The Defender.


Eugenio Derbez Interview with Dr. Anthony Fauci - Transcribed

Eugenio derbezBy Anne Dachel

Below I transcribed a brilliant recent interview of Dr. Anthony Fauci by actor, director, producer, Eugenio Derbez.

I have to think that Fauci agreed to this 30 minute talk in order to give himself an opportunity to promote the COVID 19 vaccine to Hispanic Americans.

 The big surprise was that Derbez knew what to bring up about the development and safety of the COVID19 vaccines. He actually asked questions you will never hear from anyone in the mainstream media.

Derbez wanted to know why we should trust vaccines with only months of trials, not years and only Emergency Use Authorization from the FDA.

What about the lack of liability on the part of vaccine makers and side effects that don’t show up 5 to 10 years down the road?  Derbez  pressed these points repeatedly.

What about the new mRNA vaccines? Derbez wanted to know if this “technology [has] ever been injected into humans before.”

Fauci had to admit it hadn’t, but he wasn’t worried because “the results are really, really good.”

 Fauci was equally untroubled when Derbez questioned the controversial use of aborted fetal cell lines in vaccine manufacture. Derbez said it was of concern to many Hispanic Catholics. 

Fauci noted that only “some” bishops advised against the Johnson and Johnson COVID vaccine because of fetal cell use.

Derbez brought up asymptomatic spread of the virus, along with the effectiveness of the COVID19 vaccines.

Fauci danced around the possibility that these vaccines stop transmission, provide immunity or merely reduce symptoms. If you listen to the end, he seems to say they do all three. If everyone in the family is vaccinated, or if only grandma is, you can gather “in the home” without masks, hugging and kissing everyone.

I was left with the overwhelming feeling that the COVID 19 vaccines pose lots of questions with few answers.

Mar 13, 2021,  EUGENIO DERBEZ INTERVIEWS DR. FAUCI https://www.youtube.com/watch?v=NiB3eK3btOE

1:59

Derbez: Let’s get straight to the point. I was telling people I was a little bit concerned, so I had a lot of doubts about this vaccine, and then I got the invitation to talk to you.

It would be very helpful for all of us to learn and to understand about the vaccine.

So, first question: which of the COVID 19 vaccines have been officially approved by the FDA?

Fauci: Three of them. One from Moderna, which is the mRNA vaccine.

One from Pfizer, which is another mRNA vaccine.

And the other one is from J and J, Johnson and Johnson, which is a little bit different.  It gives the same kind of response, but it’s a little bit different.

So there are three vaccines that have gotten emergency use authorization from the FDA so far.

There are a couple of others that are still being tested to determine if they’re safe and effective, but the three that I just mentioned, have been shown in very large clinical trials involving anywhere from 30,000 to 44,000 people per trial, were shown to be not only very efficacious, but  quite safe.

3:35

Derbez:  …What is the difference between emergency use authorization and an official approval by the FDA?

Continue reading "Eugenio Derbez Interview with Dr. Anthony Fauci - Transcribed" »


Risk of Stroke Events Cause Alarm in Europe Not USA

Stroke c vax
Source https://medalerts.org/


Much of Europe is halting the use of the Oxford Astra Zeneca Covid jab as a precaution about blood clots. We are not employing the OAZ jab here in the USA,  but there are reports of similar events happening on our VAERS system (see graphic above) with the vaccines being administered to citizens here in the USA. Maybe your loved one.  Maybe you. You'll likely never hear about it on the news where you are being spoon fed unicorns and rainbows to ensure vaccination compliance. But we are not compliant. Nor will be complicit. We know the horror of vaccine injury and death. So many of us kiss our kids goodnight while they sing Sesame Street or Barney songs because of their early vaccine injury.  Americans and citizens around the world are learning like we did, the painful way. We're gonna need a bigger.... blog.

Doctors baffled as countries suspend use of AstraZeneca vaccine over blood clot fears

Sweden and Latvia on Tuesday joined a fast-growing list of European countries suspending the use of the vaccine as a precautionary measure following reports of blood clots.

Germany, France, Italy and Spain on Monday said they would all stop administering the shot.

The World Health Organization, Europe’s drug regulator and the International Society on Thrombosis and Hemostasis have all recommended that countries continue to use the Oxford-AstraZeneca vaccine.

“Halting a vaccine roll out during a pandemic has consequences,” said Dr. Michael Head, senior research fellow in Global Health at the University of Southampton, U.K.


Marvelous Marvin Hagler's Death Unexpected Like Hank Aaron's

98E1E1D3-62D3-46D9-8845-D673D5F30310Boxing legend Marvelous Marvin Hagler died over the weekend causing a rash of speculation. Former opponent Thomas Hearns asked for prayers and said that Hagler was in the ICU following an adverse reaction to his Covid jab. His family later said he died at home "unexpectedly."

"Madness ensued" online.

Hagler was 66 years old. I believe our own Dan Olmsted would have been 66 this year  himself.

Earlier this winter, baseball and civil rights hero Hammerin' Hank Aaron died just two weeks after his very public, on camera vaccination. He was older than Hagler, but said to have been in good health and also died unexpectedly. Two African American males, sports legends. In a normal world, experts would be rushing to discover if there was any correlation to the vaccination. We do not live in a normal world. Those of us in the autism vaccine injury community have known what millions of formerly naive Americans are now discovering. Vaccines, unlike the doctors who administer them, can DO NO HARM. Not by design. By edict.

Rest in peace Marvelous Marvin.


The Facebook Culling Deletes 39 Year Old National Vaccine Information Center

We were disheartened to read yesterday that Facebook has removed the NVIC page. Barb Loe Fisher has been a champion for the right to informed consent, safety and choice for vaccination for more than 40 years, as result of her own son's injury. 

Kim Bella Barbara 2010
Kim and Bella with Barb, 2009

NVIC has always been a resource for factual information about vaccination safety, informed consent and State by State updates on religious, philosophical and medical exemptions. It is a goldmine for thinkers. And a NVIC banned from FBthreat to the pharmaceutical warmongers who are the new ruling class, protected by Big Tech. Facebook removed their page yesterday.

Visit NVIC.org here.


WHO Announces Global No Fault Covid Vaccine Injury Compensation Program

Lucy-footballA Global Compensation Program?

By Wayne Rohde Feb 23, 2021

On Monday, Feb 22, 2021, The World Health Organization (WHO) announced a no-fault injury compensation program for COVID-19 vaccines. WHO has designated 92 low- and middle-income countries and economies eligible for support via the GAVI COVAX Advance Market Commitment (AMC) of the COVAX Facility.[1]

The COVAX Facility is co-led by the Coalition for Epidemic Preparedness Innovations (CEPI), Gavi and the World Health Organization (WHO), the United Nations and alongside key delivery partner UNICEF. Its aim is to accelerate the development and manufacture of COVID-19 vaccines, and to guarantee fair and equitable access for every country in the world.[2]

Gavi, created in 2000 with start-up funding from the Bill and Melinda Gates Foundation, is an international organization -- a global Vaccine Alliance, bringing together public and private sectors with the shared goal of creating equal access to new and underused vaccines for children living in the world's poorest countries.[3]

With this announcement, WHO is promoting this compensation program as the world’s first global program to provide for those who have suffered allegedly rare, serious adverse events associated with COVID-19 vaccines. In the COVAX announcement, it appears that the cutoff date, or statute of limitations to file a petition, is June 30, 2022.

Creating a compensation program is not a new process for the WHO or United Nations. After the Iraqi invasion of Kuwait, the United Nations created the UN Compensation Commission in 1991, evaluating nearly 2.7 million claims and issuing 1.5 million awards, totaling over $50 billion dollars.[4]

As early as 2006, the International Federation of Pharmaceutical Manufacturers and Associations, the global pharmaceutical-industry lobbying group, publicly demanded that manufacturers be granted liability protection from vaccine-related adverse events if they were going to participate in pandemic response initiatives.[5]

The world has attempted to control other epidemics through the use of vaccines to mitigate the spread of the disease. During the 2009 H1N1 outbreak, one specific vaccine used in the UK and Northern Europe caused an increase in narcolepsy, which resulted in substantial compensation claims.

During the Ebola outbreaks in Western Africa, some nations refused to accept liability for vaccine injuries. The dilemma for these nations and others that are considered low income involves whether to continue to refuse to offer manufacturers liability protection or to go without vaccines. In the current situation, that means going without COVID-19 vaccines. Is the end game for this collaboration, to allow pharmaceutical industry to remove itself from any liability and member nations to cede away their citizens and the nation’s right to sue for damages?

The COVAX compensation program will start on March 31, 2021 through its web portal (www.covaxclaims.com). Individuals who have been injured may apply for compensation for a COVAX vaccine administered before March 31, 2021.[6]  The funding will come from a levy on all distributed COVAX-19 vaccines.

Continue reading "WHO Announces Global No Fault Covid Vaccine Injury Compensation Program" »


Animation Video Q&A about the Moderna & Pfizer Products

Covid Animation screen group
View A Crash Course on the COVID Vaccine at Millions Against Medical Mandates

View A Crash Course on the COVID Vaccine on Rumble.

Does the COVID vaccine protect us against getting COVID? No.
Will we be able to stop wearing masks after getting the vaccine? No.
Can we end social distancing after getting the vaccine? No.


 

 

 

REFERENCES COVID VACCINE FOR VIDEO ANIMATION

1.Mayo Clinic Insights: Spreading Infection Following Vaccination

Andrew Badley M.D. - Jan 14, 2021
https://www.youtube.com/watch?v=r3krKEKCyRs&feature=youtu.be

2. Moderna boss says COVID-19 vaccine not proven to stop spread of virus

Continue reading "Animation Video Q&A about the Moderna & Pfizer Products " »


Is Death the Final Awakening?

Death is the awakeningChildren's Health Defense shared data the deaths reported to VAERS post Co Vax. We know all too well that officials and average citizens will jump through hoops, bend over backward and do anything they can to refuse to believe that the Covior (new word, Covid Savior, perfect for this Lenten season) could cause the ultimate "event."  As far as awakening, most of us haven't slept in years.

###

One-Third of Deaths Reported to CDC After COVID Vaccines Occurred Within 48 Hours of Vaccination

The numbers reflect the latest data available as of Feb. 12 from the CDC’s Vaccine Adverse Event Reporting System website. Of the 929 reported deaths, about one-third occurred within 48 hours.

According to new data released today, as of Feb. 12, 15,923 adverse reactions to COVID vaccines, including 9a29 deaths, have been reported to the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) since Dec. 14, 2020.

VAERS is the primary mechanism in the U.S. for reporting adverse vaccine reactions. Reports submitted to VAERS require further investigation before a determination can be made as to whether the reported adverse event was directly or indirectly caused by the vaccine.  Read more at Children's Health Defense.


Heart Attack IN A Stick

Heart-syringeThank you to Children's Health Defense for crunching this important safety data. VAERS is the Vaccine Adverse Event Response System, and part of the Federal government. Reports of post v a x  cardiac events are frightening. Many of us have friends and family are are getting this new product. Some of our readers are likely getting it too.  From the CHD site:

What VAERS Data Reveal About Cardiac-Related Reactions to COVID Vaccines

As of Feb. 4, 1,171 cases of cardiac-related reactions were reported to VAERS, including 134 cases where the patient died — or 21% of the total COVID vaccine deaths reported to VAERS.

We are exactly two months into the COVID 19 vaccine rollout, which began on Dec. 14, 2020. Each Friday The Defender  reports on the latest vaccine reaction numbers from the Vaccine Adverse Event Reporting System (VAERS) database.

As of Feb. 4, 12,697 reactions, including 653 deaths, had been reported to the system, out of 35 million doses of vaccines administered.

The Centers for Disease Control and Prevention (CDC) is using the VAERS system as an passive reaction surveillance tool following the fast-tracked, Emergency Use Authorization of the Pfizer and Moderna vaccines. Other systems being used are V-Safe and the Vaccine Safety Database.

We looked at the data we have so far to see if we could identify any emerging patterns. What immediately stands out is that the 12,697 reactions reported as of Feb. 4 are not limited to injection-site reactions. These appear to be serious reactions reported by medical personnel from all over the country.

One trend worth noting is the number of reported cardiological reactions, including myocardial and tachycardia disorders. We found 1,171 cases using the more common symptoms reported, including 134 cases where the patient died — or 21% of the total COVID vaccine deaths reported to VAERS.

According to VAERS data, of the 1,171 serious cardiac-related cases reported, 1,021 (87.2%) occurred within 48 hours of receiving the vaccine. Of the 134 cases where the patient died, 50% occurred within 24 hours and 60% within 48 hours.

Read more here and share with friends and especially, older family. Knowledge is sometimes scary, but so important.


How Would You Know?

Go Talk Help"The injection site was a thousand times more intense than regular shots. I felt like a full grown male punched me in the arm. It throbbed, it tingled or buzzed all the way down my arm and up into my neck. The other odd sensation was the outer rim of my ears felt like they were on fire."

That is the report of an adult after the first dose of the Covid vaccine. I'm not writing this post to question the decision of an adult to be vaccinated, and I know that this person is aware of vaccine injury, and deliberated before making a personal, informed choice. Is it the choice you or I might have made?  That's one question.  Can you afford to be sidelined for a day, a week, a month or worse?

The bigger questions speaks to the huge responsibility too many of us bear for every aspect of our children's lives. Is it the choice you or I would make for our own children with autism, whether minor or over the age of 18? After reading the above description of an actual reaction, my first thought was, "Holy cow, my daughters would be trapped in this an unable to tell me!" Can your child tell you if his or her throat is closing up in anaphylaxis? Can your child tell you if he is in severe distress? The kind that requires immediate medical care? 

Many years ago, my youngest daughter choked on a round ravioli. We did not know until she was turning blue at the table. She did not call for us in any way. She did not come to us. She did not slam the table to get our attention. She did not appear to be in distress at all - until the Heimlich was needed and used to no avail. We had to call 911. If you read my memoir a hundred years ago, this is the same child that I put to bed with a broken arm, because she was not screaming in pain.  When she arrived at the hospital, the doctors were AGHAST that she was quiet and not writhing and howling. Such is autism. So if our kids have a reaction to a Covid vaccine, it's unlikely we will have any idea at all. Or that whatever behavior changes we see, because pain masquerades as behavior,  even if WE know they are different, will be written off by medical professionals as, "just autism." Of course, one can argue  the same thing about COVID symptoms - if they worsen to a critical point and we are unaware. Here's a list of symptoms. The ones in red are physically, externally visible.

Cough
Shortness of breath or difficulty breathing
Fatigue
Muscle or body aches

Continue reading "How Would You Know?" »


Why Don't Americans Want Informed Consent?

Empty headNote: While scrolling Facebook yesterday, I came across a post from a well known, "celeb" member of our community. She was cautioning her readers to do their homework on the Covid v acc inations that are available or coming online soon. One comment caught my eye:

Please think of the fear, hesitancy and damage that comes from prematurely amplifying a potential watch on a side effect that was seen in 7 people out of a combined sample of 70,000+. (Less than .01%). Consider how many will take a riskier path and delay or avoid getting vaccinated because of the cumulative effect of these stories filling social feeds without context. The most vulnerable communities will be the most impacted.

In other words, keep quiet. Don't tell anyone about adverse reactions. It might make people think twice. No. This is not how we should operate. It's not how we are legally required to operate with drugs in the USA. I heard the most disgusting list of side effects ever on some ad on television over the weekend. But for "biologics" especially those for emergency use?  Never.

501 Deaths + 10,748 Other Injuries Reported Following COVID Vaccine, Latest CDC Data Show

These numbers reflect the latest data available as of Jan. 29 from the CDC’s Vaccine Adverse Event Reporting System website. Of the 501 reported deaths, 453 were from the U.S. The average age of those who died was 77, the youngest was 23. Read more from The Defender at Children's Health Defense.


CA Health Officials Halt Possible Hot Lot

MousetrapGame2Note: As the C Vax is rolling out across the world, there are reports of serious snags, including this story from San Diego, California below, where the Moderna vaccine was paused. As a site populated by readers affected by vaccine injury, we take no joy in these reports.  Shattered trust and lost health is nothing to gloat over.

We took a look at the dosing instructions for the Moderna version. It's complicated. Where does, and will, human error come into play as more and more "civilians" are recruited to get as many doses into as many people as possible in the shortest amount of time? Do any vaccines simply become inert and benign if administered following incorrect storage or mixing? We know that if the multi-dose Thimerosal preserved flu vaccine is not perfectly shaken, the last doses can have far more than the 25 mcg dose of mercury stated on the label. The Moderna product requires a "gentle swirl." No really, that's the exact term used in the Moderna site. Perhaps James Bond could prepare the product consistently well....  Vaccinators are expected to inspect the solution which should be "white to off-white."  Benjamin Moore paint offers more than 150 shades of white. My off white might be your ecru. Fugu is a delicacy when prepared by an expert, otherwise, it's a gamble. Are these vaccines too technically detailed to be expertly dosed in a nation where "About one-third of Americans (global literacy rate: 34%) have Level 2 literacy. ... Half of U.S. adults can't read a book written at the 8th-grade level, according to the OECD. The average American reads at the 7th- to 8th-grade level, according to The Literacy Project."

Moderna dosing

California pauses Covid-19 shots from one lot of vaccine containing more than 330,000 doses By John Bonifield, CNN Health

Health officials in California are telling medical providers across the state not to administer doses from one lot of Moderna's coronavirus vaccine while they investigate possible severe allergic reactions last week in a number of people who got shots at a community vaccination clinic.

More than 330,000 doses from the lot were distributed to 287 providers across the state from January 5-12. Tens of thousands of doses may have already been administered, but the number of unused doses is unknown, according to Darrel Ng, a spokesperson for the California Department of Public Health.

Continue reading "CA Health Officials Halt Possible Hot Lot" »


Dr. Meryl Nass: Maine EMTs Declination Form A Startling Document

LearningBy Dr. Meryl Nass, excerpted from her blog with permission. While we can, we must read everything about our healthcare choices, while they are still... choices. Dr. Nass is a physician in Maine, she was graduated from MIT and U Mississippi Medical School. Her curriculum vitae is here.

Maine EMTs being given false and frightening information they must sign to refuse a Covid vaccine

People have asked why am I not blogging about the Covid vaccines.  To be honest, I felt there was not enough information for me to be decisive, and I have been waiting for more information to become available.

However, someone called me this morning and told me about a lot of allergic reactions, including one anaphylactic reaction, at a local hospital after 30 doses were given. Staff were instructed to keep this quiet.

Today I watched a 9 minute Ben Swann video about the vaccines, in which he reads the "Declination form" that must be signed by EMTs in Maine who refuse the vaccine. It contained false and misleading statements, and I realized I should no longer delay discussing what is known about the vaccines.

  1. Both the Moderna and Pfizer vaccines are made from messengerRNA and lipid nanoparticles containing polyethylene glycol (PEG).
  2. MessengerRNA (or any RNA) can potentially be converted to DNA in the presence of reverse transcriptase.  That DNA potentially, or bits of it, could become linked to your native DNA.  While I have no idea how likely this is, I began to take the possibility seriously only after two members of FDA's advisory committee (the VRBPAC) asked about it during their meeting to approve the Pfizer vaccine on December 10.  (I watched the entire meeting and took copious notes.) Virologist tell us that much of our DNA is, in fact, originally viral DNAthat found its way in. 

I now consider the potential for vaccine RNA to be permanently inserted in my DNA a remote possibility--but one that I would like proven wrong before being vaccinated.

  1. 70% of Americans have per-existing antibodies to  PEG.  FDA suspects that these PEG antibodies may be the cause of anaphylaxis post vaccination.  The UK recommends againstpeople with severe allergic conditions receiving the mRNA vaccines. The CDC, however, recommendeds people receive it regardless of their allergy history, only asking that those with severe allergies wait an additional 15 minutes (total of 30 minutes) in the clinic in case they need to be resuscitated.  Anaphylaxis is occurring at about 10x the rate it occurs after flu vaccine (if the early numbers released by CDC are accurate).  Therefore, getting the shot in a drugstore or anywhere that trained physicians are not close by to perform a resuscitation seems like a bad idea. READ MORE HERE.

Pfizer, Moderna et al Covid Products are Medical Devices Not "Vaccines"

Ex laxThank you to Anne Dachel for working with Dr. Ken Stoller for this most interesting piece on AofA:

###

Dr. Ken Stoller of San Francisco, a longtime advocate for medical freedom, recently sent me his opinion on mandating the COVID-19 vaccine.

Below is his advice as a physician. You’ll notice that his opening argument is that it’s not really a vaccine. The COVID-19 ‘injection’ does not do what we all assume a true vaccine should do.

You are not antivax if you are against the COVID-19 injections

You are not anti-vax because the COIVD injections are not vaccines.

Yes, they are being called vaccines, but this is to bypass the regulatory requirements for a medical device.

This ‘vaccine’ is actually a medical device that has never been used in humans before and rushed to market without any appreciation for what it will do either in the short term or long term.

This injection is also being called a vaccine to gain more acceptance,  because most people assume that all vaccines are safe and effective. That’s what the CDC tells us. So if it is a vaccine, it must be safe and effective for ending the pandemic.

Some sources have indicated the adverse event rate for COVID-19  injections is as high as 80 percent, and that would include all the minor adverse events.

But if the short-term adverse event rate is 80 percent, what is in store for the long term?

They honestly don’t know and really don’t care.

Politics and eugenics, not science or good public health practices, are what is driving this grand medical experiment dwarfing the Tuskegee incident by a billion-fold.

While this is an over simplification, a vaccine, as defined by the CDC & FDA, is procedure that introduces into the body a foreign protein or weakened virus or bacteria and activates the immune system to make antibodies to same. In theory, to be effective, those antibodies actually have to perform in a useful manner.

If it works as advertised, a vaccine gets in your body and programs itself to attack the infection should it cross your path. It has to stimulate both immunity and disrupt transmission by definition, but the COVID-19  injection does not encourage your body to program your immune system. Instead, it is the program.

Continue reading "Pfizer, Moderna et al Covid Products are Medical Devices Not "Vaccines" " »


Coronavirus: BMJ urges NYT to correct vaccine 'mixing' article

Fiona_GodleeShots Fired from Across The Pond!  Pfizer's COVID vaccine administration website says that the second dose should be given 21 days later. So why is the UK government now saying the second dose will be 3 full months not three weeks later? Could it be that the second dose provides the one-two punch of more severe side effects that are sure to turn OFF first dosers who may be in line?  By waiting three months, you may have tens of thousands of first doses administered, doses that may have been refused had citizens heard about second dose adverse events.

Participants were more likely to report such symptoms following the second dose of the vaccine.

“[The reaction to the second dose] tends to be a little more of an intense response, which does make sense, considering your immune system has been exposed already,” Heinz said.

“It gets hit with another dose of [the vaccine], and it has a sort of quicker and more robust response. That makes a lot of sense immunologically,” he added. Source: www.healthline.com/health-news/what-we-know-about-the-side-effects-of-pfizers-covid-19-vaccine#Fatigue,-headache,-muscle-pain

Pfizer 21 days

https://www.cdc.gov/vaccines/covid-19/info-by-product/pfizer/index.html

From BBC News Coronavirus: BMJ urges NYT to correct vaccine 'mixing' article

The editor of the British Medical Journal has asked the New York Times to correct an article that says UK guidelines allow two Covid-19 vaccines to be mixed.

The US publication reported that UK health officials would allow patients to be given a second dose that is a different vaccine to their first.

Fiona Godlee pointed out in her letter to the NYT that it was not a recommendation.

She said the NYT's headline claiming UK guidelines say such substitutions "may happen" was "seriously misleading".

The UK has approved the Pfizer-BioNTech vaccine and the Oxford-AstraZeneca jab - but both require two doses which are now to be administered 12 weeks apart

Ms Godlee said the Joint Committee on Vaccination and Immunisation (JCVI) does not make any recommendation to mix and match - in other words, having a shot of one vaccine and then a different one 12 weeks later.


Breaking News from Corvelva

Breaking newsFrom Children's Health Defense:

Breaking! Public Prosecutor Orders Investigation Into Vaccine Quality Control and Says Scientific Answers Are Needed (Italy)

The Italian citizens’ organization Corvelva has finally forced an inquiry into the quality of vaccine lots after having financed independent analyzes of different vaccines that showed many samples are not compliant with quality standards and health product regulations.

Corvelva just issued a press release of the decision made by the Public Prosecutor’s Office in Rome on December 28th. They proudly announced that our analyzes, which had led to a complaint to the Public Prosecutor’s Office of Rome, after a request for dismissal made by the Public Minister and with our subsequent opposition last year, were today considered worthy of further study. The judge in charge issued AN ORDER in which he indicates to the Public Prosecutor the need to proceed with investigations.

Particularly interesting is a quote of this decision that emphasizes the need to provide real scientific answers and not get away with administrative or legal arguments.  “It is believed that a merely formal response to the complaint is not sufficient to overcome the technical and scientific arguments of the exponent”. This sentence was written as a response to the Public Ministry who had motivated his request to dismiss, by arguing that the effectiveness of the controls of the Italian and European health agencies “cannot be questioned by the results of the analyzes carried out by private individuals”.

The order finds that arguments of the complaint are “detailed” and that it is therefore considered necessary to investigate what was reported.

Therefore there is an indication to proceed with independent analyzes by the health security police department to see if the findings can be reproduced.

Mattia Marchi a member of the Corvelva team summarizes the whole story: Read more here.


UK Faces Food Shortages As A Result Of Conflicted Government Science

 image from www.gavi.orgBy John Stone

European countries have been shutting down their borders with the United Kingdom following advice that it harbours a 70% more contagious version of the Covid virus, which has already led to the new Tier 4 lockdown arrangements in Southern England and the effective cancellation of Christmas. Whether the mutation is actually more contagious is a matter for dispute between two Oxford professors. The case that the “strain” is more contagious has been hypothesised by the Nervtag advisory committee led by Prof Peter Horby. According to the Daily Mail Prof Horby, who is Professor of Emerging Infectious Diseases at the Centre for Tropical Medicine and Global Health, said the figure of 70 per cent was based on 'converging data'.

“He said: 'This is including, but not limited to, the rate of change in the frequency of detection of the variant (the growth rate) and the correlation between R values and the frequency of detection of the new variant.'”

This, however, is disputed by Prof Carl Heneghan of the Centre for Evidence Based Medicine. He told the Mail:

'I've been doing this job for 25 years and I can tell you can't establish a quantifiable number in such a short time frame.' 

He added 'every expert is saying it's too early to draw such an inference'.

Professor Heneghan said there was no doubt this time of the year, the 'height of the viral season', was a difficult time for the NHS. But he said failure to put out the basis of the figures was undermining public trust.

But while the mutation is already circulating in other European countries it has led to them shutting down food supplies to the UK coincidentally or not on the very verge of Brexit. Prof Horby had previously been embroiled in controversy earlier this year over the Hydroxychloroquine trial in which inappropriately high quantities of HCQ  were given to Covid patients already in a serious condition (the trial was funded by the Wellcome Trust and the Bill and Melinda Gates Foundation). Also on the Nervtag Committee is Prof Ferguson of Imperial College whose controversial modelling led to the UK’s first lockdown in the spring. Ferguson was forced to resign from the more prominent SAGE committee after breaking lockdown rules pursuing a romantic liaison, but not apparently from Nervtag. Ferguson’s Vaccine Impact Modelling Consortium at Imperial College is also funded by the Bill and Melinda Gates Foundation as well as the global vaccine alliance, GAVI. Ferguson's group was said to have received $185 million from the Bill and Melinda Gate Foundation between 2006 and 2018.

Converging data or converging interest?


Doctors Believe In Santa More than Vaccine Side Effect Injury

Doctor Hand UpRepeat after me. "A side effect is an injury. A side effect is an injury. A side effect is an injury." Side effects, also known as adverse events, are unwanted or unexpected events or reactions to a drug. Side effects can vary from minor problems like a runny nose to life-threatening events, such as an increased risk of a heart attack. Source FDA.gov

Sure, there are times when the "side effect" is considered beneficial.  Like The Little Blue Pill from Pfizer. Sildanifil was originally a hypertension drug. Viagra has been great for Pfizer's bottom line. But the term is used most often to describe a negative outcome.

Reports of vaccine "side effects" are pouring in on every Covid vaccine, and vaccine "exemptions" are in the news, (my God the irony, as doctors are being penalized for writing exemptions for children.)  The most newsworthy is the allergy warning with the Pfizer vaccine that President Trump is trying to hoard here in the USA. Allergy warning for Pfizer/BioNTech vaccine after UK health workers with allergy history suffer reaction  Many years ago, egg allergy was REMOVED as a contraindication to the flu vaccine, many readers will recall.  Just like that! A roadblock to vaccination was torn down. For years, pharmacists have routinely asked potential flu vaccine recipients if they are allergic to eggs. Now, there is no need for that question, according to updated guidelines from American College of Allergy, Asthma and Immunology (ACAAI). The issue has been that most influenza vaccines are grown in eggs and contain tiny amounts of egg protein. Multiple studies have shown, however, that the risk to patients with egg allergies is small and not much different for others getting influenza vaccines, notes the article in Annals of Allergy, Asthma and Immunology. Source US Pharmacist

Doctors believe Santa will pop down the chimney in two weeks more than they believe in vaccine injury. I want to remind our readers that David Tayloe, the then President Elect (no not that one) of the American Academy of Pediatrics said in 2008 that he had NEVER referred a child to the vaccine injury compensation program in decades of practice. Not one. Nada. Either he had never once seen injury or he never recognized it, or, darkest thought of all, he saw it and never told or assisted the family.

I have no confidence that medical professionals will protect patients from the plethora of Covid vaccines. They fear losing their ability to practice medicine. They fear being shunned by fellow doctors. They fear being shamed in the news. They fear losing insurance carrier affiliations. They just don't seem to fear vaccine side effects.

CNN transcript April 2, 2008

DR. DAVID T. TAYLOE, JR.. PRESIDENT-ELECT, AMERICAN ACADEMY OF PEDIATRICS: Well, first of all, the childhood vaccine program is the most beneficial public health program in the history of mankind.

Continue reading "Doctors Believe In Santa More than Vaccine Side Effect Injury" »


Covid Driving a Runaway Train of US Vaccine Compensation Programs

YOYOBy Wayne Rohde

That phrase could be used for so many different scenarios. But one of the most extreme and dangerous scenarios is being played out right now. How our Government is plowing full speed ahead without any concern for the collateral damage it will cause in its quest to provide a COVID vaccine.

I am not going to talk about the science of the vaccines. That is being discussed so many other places.

I want to discuss how our Government is setting up the existing compensation programs for vaccine injury to fail, thus denying any type of future compensation for those who are injured because of the COVID vaccine and possible future new vaccines.

The COVID vaccine is on track to be released first to a designated group of health care workers and residents of senior living facilities. Then as more of the vaccine becomes available, then high-risk candidates due to their medical condition, and finally the general public. This might take 6 months or longer.

And we are starting to read a growing number of medical organizations are saying no. Same for first responders. No one is defending our seniors. And that is a tragedy.

But what happens to anyone that is injured from a COVID vaccine? Their options seeking compensation are extremely limited. The CounterMeasures Injury Compensation Program (CICP) is your only option. It is not equitable, not efficient from the petitioner’s point of view, and it is not fair. It is extremely difficult to prevail. Currently 8% of all petitioners since 2010 have been awarded compensation. It has been said, “the CICP is a program where you have the right to file and loose.”

I wrote about the CICP last month, “Why injuries suffered from the COVID-19 vaccines need to be litigated in the NVICP.”

The program does not provide reimbursement for legal representation or medical expert fees. The vast majority of us will not be able to afford these fees, generally ranging between $25,000 for shoulder injuries in the NVICP to $250,000 and up for more complex and protracted cases.

The program does not award pain & suffering awards. In the NVICP, this benefit can be awarded up to max of $250,000.

The program does pay for lost wages. However, future lost wages issue has not been settled. The CICP does pay for unreimbursed medical expenses. What is unclear is whether or not the program will pay for lifelong care.

Continue reading "Covid Driving a Runaway Train of US Vaccine Compensation Programs" »


Anaphylactic Reaction Reported after Pfizer Jab in UK

Epi-pen What this article is calling for is called a "Medical exemption." Shall we spell it?   Medical exemptions are UNDER ATTACK in the United States, with physicians losing their autonomy to write them for pediatric patients for many years now. 

California Law to Restrict Medical Vaccine Exemptions Raises Questions Over Control Restricting vaccine exemptions has raised questions of whether the actions of many states like California have exceeded legal and ethical limits of power.

Isn't it ironic that COVID is exposing the problems and issues we have faced with vaccine injury for decades as if it's all something brand spanking new? I believe President Trump is fighting to make sure the USA gets first dibs on the Pfizer brand vaccine. We're gonna need a bigger swamp.

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Covid-19 vaccine: Allergy warning over new jab By Nick Triggle and Rachel Schraer

People with a history of significant allergic reactions should not have the Pfizer/BioNTech Covid jab, regulators say.

It came after two NHS workers had allergic reactions on Tuesday.

The advice applies to those who have had reactions to medicines, food or vaccines, the Medicines and Healthcare products Regulatory Agency said.

The two people had a reaction shortly after having the new jab, had treatment and are both fine now.

They are understood to have had an anaphylactoid reaction, which tends to involve a skin rash, breathlessness and sometimes a drop in blood pressure. This is not the same as anaphylaxis which can be fatal.

Both NHS workers have a history of serious allergies and carry adrenaline pens around with them.


Do You Trust A Pharm Tech to Administer the Most Complex Vaccine In Human History

CVS Pharma Tech Covid
CVS is hiring THOUSANDS of pharmacy technicians and pharmacists to administer the Covid vaccine.

Pharmacy interns and techs who meet HHS requirements can administer childhood, COVID-19 vaccines

I am not belittling the career choice of pharma tech. But you should know that a person with a high school diploma or GED who makes $21,000 will be injecting you with this brand new vaccine. A Pharmacy Intern is a pharmacy school student. The vaccine needs to be stored, thawed, mixed, spoken to in a soft voice and told that it is the prettiest vaccine ever according to documentation. UK Pfizer Covid Doc - Read it

Salary for a Pharm Teach ranges from high $20Ks to low $30Ks. Source Zip recruiter

From the CVS hiring site:

Education:
High School diploma or equivalent (preferred).

UK Pfizer Covid Doc - Read it

The rushed vaccine is gasoline. Add human error? 

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F8F45C20-ACD3-4E3C-85D0-AB3F838ED631



The COVID Vaccine: Yes or No?

Yes or noNote: Thanks to Dr. Richard Moskowitz, Harvard and NYU trained MD and author of Vaccines A Reappraisal, for his opinion piece on CoVax.   Dr. Moskowitz is a friend of AofA, I've had the pleasure of meeting him.  His article below puts in basic terms you can share the situation with CoVaxes. Sadly, I agree with him, many people outside our knowledge base will take these vaccines thinking they will streamline their lives. Instead, many will be sidelined.

By Dr. Richard Moskowitz

First of all, I doubt that any of the vaccines will work very well.  Since the SARS in 2002, there have been many attempts to make a vaccine against coronaviruses, and they've all failed, for many of the same reason that the flu vaccine has failed, because the viruses are so mutable that, by the time you make the vaccine, the virus is already different.  So Vaccines Richard Moskowitzthey do a new flu vaccine every year, and they're probably going to do that here, too, but they often don't fit that well.

Second, they are using a new technology that's never been used on humans before, because they can produce a vaccine much faster, without having to culture the virus, by just splicing viral RNA into the genetic material of the cell, so it will respond without having to introduce the virus from the outside, so to speak.  They claim it's only the messenger RNA of the mitochondria, not the DNA of the nucleus, so it won't find its way into the gene pool, and turn you and your descendants into GMO's; but I'm less sure of that, and I seriously doubt they have any clear idea of the long-term consequences of monkeying around like that, or even that they're interested or concerned about it.

And third, if the end result is the same, if they accomplish basically what the old vaccines did, that would be reason enough to avoid them, because of their propensity to bring about chronic, autoimmune phenomena and eventually, in many people, overt autoimmune diseases, at the very least making worse the ones that are already there, which most of us have some form or trace of.

Continue reading "The COVID Vaccine: Yes or No?" »


Moderna Vaccine Designed in..... 2 Days

Impossible things 2Imagine dining in a restaurant that served your turkey dinner at 120 degrees Fahrenheit (180 degrees is safe), charged you $500 a plate, and then had no liability when you ended up passed out on the bathroom tile from food poisoning. And then it got a 5 star review.

BusinessInsider.com reports that the Moderna vaccine was designed in 2 days.

Moderna's coronavirus vaccine candidate was found to be 94.5% effective in preventing COVID-19 in clinical trials, the company announced last week.

The vaccine's development process was unprecedentedly fast — only the team of Pfizer and BioNTech beat the biotech newcomer in announcing results from a late-stage clinical trial.

The experimental vaccine was also far more effective than expected: The Food and Drug Administration had said it would likely approve a vaccine that showed at least 50% efficacy, and Dr. Anthony Fauci had said he hoped for 70%. (AstraZeneca found its coronavirus vaccine candidate to be 70% effective on average, while Pfizer-BioNTech reported their shot is 95% effective.)

But perhaps more remarkable is that Moderna designed its vaccine in just two days in January, before some people had even heard of the coronavirus....


AstraZeneca Math: 62% is 90%

Dunce girlIf I told my parents I got a 90 on my test, and the paper said 62, I'd have been sent to my room without any supper.  Not at all surprised by the lies, pharma has staked its very existence on the CoVax. It's the biggest cash grab since Bernie Madoff.

AstraZeneca Covid vaccine study results clouded by manufacturing error

“You’ve taken two studies for which different doses were used and come up with a composite that doesn’t represent either of the doses," an expert said.

LONDON — AstraZeneca and Oxford University on Wednesday acknowledged a manufacturing error that has raised questions about their Covid-19 vaccine after revealing earlier this week it was “highly effective” against the disease.

On Monday, researchers said AstraZeneca vaccine had an efficacy of up to 90 percent when half a dose was administered followed by a full dose. That efficacy rate is on par with other vaccine candidates announced by Pfizer and Moderna earlier this month. In the group that got two full doses, the vaccine appeared to be 62 percent effective. Combined, the drugmakers said the vaccine appeared to be 70 percent effective.


Covid 19 Vaccine Injuries Deserve Litigation in the National Vaccine Injury Compensation Program

Right On Point Screen
Why injuries suffered from the COVID-19 vaccines need to be litigated in the NVICP

By Wayne Rohde

There is a lot of speculation on where any injuries or death suffered by the American public will be adjudicated once COVID-19 vaccines are approved and distributed. There are two specific and distinctive federal programs that compensate for vaccine injury or death.

The first, the more commonly known of the two, the National Vaccine Injury Compensation Program (NVICP) and the second, a more secretive program called the CounterMeasures Injury Compensation Program (CICP).

The NVICP provides compensation for the approved vaccines for children and adults that are recommended for normal vaccination. The CDC via the Advisory Committee on Immunization Practices (ACIP) will approve a vaccine for administration for children or adults or both. The Secretary of HHS must announce the intent to add the vaccine to the schedule and allow public comment on the addition. Congress weighs in to add a $0.75 if it is a new class of vaccines.

The Federal Court of Claims will adjudicate the petition for any injury or death. The petitioner can appeal to a higher court, all the way up to the Supreme Court if able.

The CICP is entirely different and very problematic. 

In the aftermath of the Sept. 11, 2001 terrorist attacks, Congress created the CounterMeasures program to speed compensation to people injured from drugs, vaccines, and devices developed in response to pandemics and national security events. Those included biological warfare and radiation poisoning. A few of the vaccines in that category are for anthrax, ebola, and zika.

The CICP is designed to handle pandemic or other health emergency countermeasures as declared by the Secretary of HHS. And will be the likely landing spot initially for any injuries or deaths alleged as a result of receiving a COVID-19 vaccine. 

The CICP is considered the black hole. And for good reason. I will give you several.

Continue reading "Covid 19 Vaccine Injuries Deserve Litigation in the National Vaccine Injury Compensation Program" »


As if Vaccine Safety Was Ever a Priority

Blame-300x300Pharmacist.com picked up a NYT story from last month accusing President Trump of decreasing vaccine safety. Where to begin on that one? Maybe 13 years ago to our inception? Maybe to 1986? Wouldn't it be something if the Trump cum COVID era brought "everyone" into the "anti-vax" fold? If I could figure out how to run this post inside out and backwards, I would. That's how everything feels right now.

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The Trump administration shut a vaccine safety office last year. What's the plan now?

Tracking outcomes in COVID-19 vaccine recipients to ensure the product is not causing harms after coming to market is an enormous undertaking, one that could be challenged further considering changes last year to the National Vaccine Program Office.

Tracking outcomes in COVID-19 vaccine recipients to ensure the product is not causing harms after coming to market is an enormous undertaking, one that could be challenged further considering changes last year to the National Vaccine Program Office. After its purported closure, experts complain the task now falls to a patchwork of federal agencies—including FDA and CDC—with no central leadership behind the effort. A spokesperson with HHS, however, denies that the vaccine office was shuttered. "The office was not 'closed,' but was merged with the Office of Infectious Disease and HIV/AIDS Policy and was strengthened," the spokesperson noted in a statement. "All the functions continue in this new organizational structure." Technicalities aside, critics remain concerned about a lack of coordinated direction that would normally have come from the vaccine office, as well as the absence of a plan to communicate findings to the public. FDA responds that it will post updates via its website, while CDC will hold public meetings. The agencies will retrieve data from various monitoring systems, including smartphone apps, a database of electronic health records and insurance claims, and CMS data on people aged 65 years and older.


Citizen Petition and a Petition for a Stay of Action

B5EB5444-CA7D-4AFD-A9B2-9AB26C6E26D7On November 6, 2020, ICAN filed a Citizen Petition and a Petition for a Stay of Action demanding that the FDA require valid endpoints for determining efficacy in the COVID-19 vaccine trials currently being run by Pfizer, Moderna, AstraZeneca, and Johnson & Johnson.  ICAN’s demands include that the vaccine be shown to prevent serious cases of COVID-19 (not just mild cases) and that it can stop transmission of COVID-19.

As explained in our previous legal updates, ICAN’s legal team has been hammering away at the safety requirements for the clinical trials of COVID-19 vaccines, including demanding they be placebo-controlled, long-term, and have other safeguards.  Many of those demands were subsequently met and we are not done fighting on that front.  But there is now another battle we are fighting. 

ICAN’s legal team, led by Aaron Siri, has now also focused its efforts on the basis the FDA will rely upon to determine whether any of the COVID-19 vaccine frontrunners are effective.  Many Americans have been led to believe that the vaccines currently in trials are the answer to all pandemic-related problems.  Many believe this is because a vaccine, when available, will prevent individuals from having a serious case of COVID-19 and will stop people from spreading it to others.  However, the clinical trials for Pfizer, Moderna, AstraZeneca, and Johnson & Johnson’s products are not designed to determine either of these! 

Instead, each of the four trials’ primary goals for determining whether the vaccine is effective merely requires determination of whether it can reduce symptoms of mild cases of COVID-19.   The trials will also not demonstrate whether or not a vaccine recipient can still transmit COVID-19 to others.  This means that, under the current rules, a COVID-19 vaccine can be licensed without demonstrating it can prevent severe COVID-19, hospitalization, or deaths, nor stop the spread of COVID-19.

Also concerning is that “cases” of COVID-19 for trial purposes are being demonstrated by positive PCR tests.  The scientific literature has shown that such PCR tests can be highly unreliable, frequently giving false positives.  Consistent with this literature, we demanded that only positive PCR results meeting certain criteria be relied upon.  ICAN also demanded that all participants be tested before and after vaccination for T-cell immunity to SARS-CoV-2, which is not currently part of the protocols.  If a person has pre-existing immunity to SARS-CoV-2 (either from being exposed to COVID-19 or otherwise) their presence in the study could affect the result by showing fewer people getting sick than would actually occur in the “wild.”

These alarming deficiencies in the studies were what led ICAN to direct its attorneys to file a petition demanding that all four Phase III COVID-19 vaccine trials amend their efficacy endpoints.  ICAN demanded, among other things, that the trials test and determine (1) whether these vaccines will prevent severe cases of COVID-19; and (2) whether they will stop the spread of the virus.  ICAN further demanded improvements in the PCR testing protocol and T-cell testing pre-and-post vaccination.

Recognizing the critical importance that these changes be made in a timely manner, on November 11, 2020, ICAN’s attorneys filed a Petition for a Stay of Action with the FDA which asks that the agency stay, or pause, any action related to the trials until the requested actions in the efficacy petition are implemented.

ICAN’s attorneys separately sent a letter to Dr. Peter Marks, the Director of the Center for Biologics Evaluation and Research at the FDA, bringing these very concerns to his attention.  You can read that letter hereDr. Marks has referred to himself as “the FDA point person on COVID-19 vaccines” and has assured Americans that the FDA “will make sure they’re safe and effective.”  ICAN will closely review any response from Dr. Marks given his promise that he and the FDA “uphold globally respected standards for product quality, safety, and efficacy” and his statement that he would resign if “something that was unsafe or ineffective [] was being put through.”

Continue reading "Citizen Petition and a Petition for a Stay of Action" »


Right on Point Podcast Does SCOTUS Have Authority to Mandate A Vaccine

Right on Point

Listen HERE

Updated link! Apologies.


Wayne Rohde for Episode 1 - Mary Holland and Wayne Rohde discuss the 1905 US Supreme Court decision on whether or not the state has the authority to mandate a vaccine and how this relates to current day debate of a COVID vaccine mandate.

Right on Point podcast hosted by Wayne Rohde examines legal rights and issues surrounding the National Vaccine Injury Compensation Program aka (The Vaccine Court), the PREP Act, the CounterMeasures Injury Compensation Program, and legalities of possible mandates of a potential COVID vaccine.

Mary Holland, Children’s Health Defense’s vice chair and general counsel, discusses the 1905 US Supreme Court decision Jacobson v State of Mass. Mary breaks down the decision and how it is applied today by courts and state & federal government. Mary and Wayne discuss the issue of whether the federal government mandate a COVID vaccine.


Adjuvants: The BBC's Fairy Dust Future

image from external-content.duckduckgo.comby John Stone

Two days ago I received at breakfast a magazine article from an outfit called BBC Future entitled Immune Respose: The Strange Ingredients Found in Vaccines by Zaria Gorvett (pictured left).That the BBC should supply such a bland and poorly informed article for the popular market is no surprise, but nevertheless my annoyance did rise at her account of the DPT affair, and I wrote to her:

Dear Ms Gorvett,

Re: Your article “Immune Response” this morning

Despite the opprobrium heaped on John Wilson the government discreetly paid out on 600 DPT cases within three years of the vaccine damage payment act of 1979. In a letter last year to BMJ (which I append)  I also pointed out the paper by Mogensen which found that mortality in DPT vaccinated infants in Guinea-Bissau (1981) was 5 times vaccinated. This is not a small matter.

I also point out that size comparison makes no sense when talking (about)  an active ingredient of a product and I forward the link to the recent article by Prof Exley “An aluminium adjuvant in a vaccine is an acute exposure to aluminium”.

It is not correct to say that there is no evidence when there is evidence and I think you ought to reconsider.

Yours sincerely,

 John Stone, UK Editor, Age of Autism

The Benefits of DPT

(BMJ Rapid Response)

Mara Kardas-Nelson [1] should also note that as result of DPT controversy and the UK Vaccine Damage Payment Act of 1979 there were 600 payments in the period 1978-81 (1978/9: 36, 1979/80: 317, 1980/1: 256) [2,3]. The rhetoric behind the legislation was that injuries were rare but this was not borne out by the record [2,3]. The act enabled the government to retrieve the reputation of the programme amid adverse publicity by acknowledging the principle of harm but no one knew how many awards there had actually been - and initially there were a lot. This would also not take account of any deaths.

According to Mogensen et al, the introduction of DPT to Guinea-Bissau in 1981 was associated with a 5 fold increase in the rate of death [4]:

"Among 3–5-month-old children, having received DTP (±OPV) was associated with a mortality hazard ratio (HR) of 5.00 (95% CI 1.53–16.3) compared with not-yet-DTP-vaccinated children. Differences in background factors did not explain the effect. The negative effect was particularly strong for children who had received DTP-only and no OPV (HR = 10.0 (2.61–38.6)). All-cause infant mortality after 3 months of age increased after the introduction of these vaccines (HR = 2.12 (1.07–4.19))."

[1] Kardas- Nelson, 'Despite high rates of vaccination, pertussis cases are on the rise. Is a new vaccination strategy needed?', BMJ 2019; 366 doi: https://doi.org/10.1136/bmj.l4460 (Published 09 July 2019)

[2] Gareth Millward, 'A Disability Act? The Vaccine Damage Payments Act 1979 and the British Government’s Response to the Pertussis Vaccine Scare', Social History of Medicine, Volume 30, Issue 2, May 2017, Pages 429–447, https://doi.org/10.1093/shm/hkv140

[3] 'Annex A - Vaccine Damage Payments claims received and award statistics', https://www.whatdotheyknow.com/request/242813/response/599844/attach/3/A...

[4] Mogensen et al, 'The Introduction of Diphtheria-Tetanus-Pertussis and Oral Polio Vaccine Among Young Infants in an Urban African Community: A Natural Experiment', Ebiomedicine March 2017, https://www.ebiomedicine.com/article/S2352-3964(17)30046-4/abstract

I forgot to mention that the old DPT contained 50 micrograms of life-enhancing ethyl mercury but not receiving  an answer I decided to forward it to her editor Amanda Ruggeri (below), who describes herself on her website as  “Journalist, Photographer, Traveler,  Historian,  Adventurer”, and obviously a very exciting person. She also has not replied. image from external-content.duckduckgo.com

What I did not know at the time that I wrote to Zaria was that before writing her amusing vaccine fairy story she had interviewed Prof Exley at length on the phone. Yesterday, he wrote to her furiously:

Dear Zaria,

This not about whether one 'likes' something or not. It is about your integrity as a journalist.

You contacted me by email to ask my advice. I was happy to help and even gave you my home telephone number since you wished to talk to me personally and not simply correspond by email.

We talked for about forty minutes. I shared with you a great deal of scientific, published, information on our expertise in aluminium adjuvants used in vaccines. I made sure that you had access to all the primary published research that we talked about. I also gave you some background on adjuvants generally. You gave the impression of both being very interested in the information I gave you and also of being grateful for my time and expertise. Afterall we are, arguably, the world's leading group researching the efficacy and safety of aluminium adjuvants used in vaccines.

When we finished our conversation, you promised to send me a link to your article. You did not do this and reading your article, I can understand why.

Not only did you not mention my contribution to your article once but when opportunities arose you chose to write what can only be described as blatant lies.

For example, even though you knew that what you had written was untrue you still wrote;

There is as little as 0.2mg of aluminium in a typical vaccine dose, which is equivalent to less than the weight of a single poppy seed. There is no evidence that any of the adjuvants currently in use lead to side-effects.

Apart from being factually incorrect the comparison with a poppy seed is absurd at best.

What happened to your editor's mantra concerning BBC Future;

We believe in truth, facts, and science. We take the time to think. And we don't accept — we ask why.

I told you everything you needed to know about how much aluminium is used in vaccines. I even shared with you some of our new research in this field about to be published in the BMJ. I pointed out to you that there are serious adverse events caused by aluminium adjuvants and I also informed you as to where you could find this information, no lesser document than the patient information leaflet provided with every vaccine.

Your writing about DPT is completely false and while we did not discuss this you could have checked this information with me at any time. You clearly chose not to check your information.

I told you the story of Glenny and the 'discovery' of aluminium adjuvants.

I also made sure that you understood which aluminium salts were used as aluminium adjuvants. Instead you wrote lies again about this;

To this day, the aluminium in vaccines is always in the form of salts. These include aluminium hydroxide (commonly used as an antacid to relieve indigestion and heartburn), aluminium phosphate (often used in dental cement) and potassium aluminium sulphate, which is sometimes found in baking powder.

You decided instead to write complete scientific nonsense in your descriptions of aluminium salts used in vaccines, why is beyond me when you had access to the correct information. What were you trying to do, make the aluminium salts sound benign by comparing them wrongly to household products?

I told you that the main reason why aluminium adjuvants are effective is because they are toxic at the vaccine injection site. I spoke to you at length about this and I pointed you towards the relevant peer reviewed published scientific literature. Your reference to uric acid at this point did not come from me and has no relevance.

This article is very shoddy journalism. It seems to have been primarily informed by a Chinese scientist working on vaccines in China. As the world's leading researcher on aluminium, I have no knowledge of this scientist only that they have no expertise in aluminium adjuvants. Why you chose to only follow their advice is insulting.

If you and your editors do truly 'believe in truth, facts, and science', then I would expect a right of reply to this inaccurate and scientifically inept article. To not do so would suggest that the written lies therein have an alternative agenda.

Yours sincerely

image from i.ytimg.com

 

 

 

 

 

Professor Christopher Exley PhD FRSB

So far, at the time of writing, Prof Exley assures me he has heard neither from Zaria Gorvett or her editor Amanda Ruggeri (which is I suppose what you would expect from the modern BBC). Perhaps as their next assignment these two geniuses can set themselves to working out why Autism Spectrum Disorders have reached 7% in Belfast schools (I have had an identical figure just quoted me by personal communication for the first year in-take of a Welsh comprehensive school). All brought to you by the BBC’s responsible journalism.

Post Script

Prof Exley has now received a succession of letters from the BBC which does not make their position any more satisfactory:

Dear Professor Exley,

Thank you very much for speaking with me the other day. I am sorry that you do not like the article. I have cc'd my editors.

Best regards,

Zaria  

*

Dear Prof. Exley,

Thank you for raising your concerns with BBC Future. We’re sorry that you feel your time in the interview was wasted; we seek information from a wide range of sources, and there is no guarantee when we do interviews that any given interviewee will be quoted or mentioned in a piece.

We’ve gone through the claims you make below and remain confident in the accuracy of our reporting. Thank you again for your time.

Best,

Amanda Ruggeri

*

Dear Professor Exley,

I’m the Editorial Director for the BBC’s international news and features output.    Amanda has passed your complaint onto me.

Let me echo Amanda’s apology for the fact that you feel your time was wasted.    We speak to a lot of people in the course of our research and are grateful to anyone who gives up their time. 

The article was amended on Thursday to clarify two points:

The weight of evidence is that adjuvants do not lead to serious side-effects.

And we added detail about the link between the pertussis vaccine and encephalopathy and corrected the statement that the vaccine had been administered for decades without incident.

Best wishes,

Mary

Mary Wilkinson, Head of Editorial Content,  BBC Global News  Ltd

Of course, no one actually says sorry for their actions, and all three are guilty of deliberately misleading the public by failing to report that they had consulted him and received  information of substance (existing in the form of peer reviewed studies in respected journals)  which stood in contradiction to the claims of the published article. If they were professionally fearful of the consequences of publishing this information then it might have been better not to publish at all. Plainly none of them have the expertise to discard Prof Exley's evidence and there is no explanation of why they chose to do this except expedience.


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.)

https://www.congress.gov/bill/116th-congress/house-resolution/1154/text

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.

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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
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
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"

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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.

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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.