Showing posts with label Guillain-Barré. Show all posts
Showing posts with label Guillain-Barré. Show all posts

Did Gavin Newsom & Justin Bieber Have Bell's Palsy From Vaccines?

Justin Bieber Bell's Palsy
Bells Palsy Gavin Newsom
Gavin Newsom Bell's Palsy
2 Sources for this story below . . . 

Justin Bieber reveals he has Ramsay Hunt syndrome

Twitter suspended the VaccineTruth2 account

Want to know which article that they do NOT want you to see? It's the article showing Bieber's paralysis was 99% likely to have been caused by the vaccine.

They do not want you to learn the truth about Justin Bieber’s injury. They want you to believe the fairy tale that Bieber and his wife are just super unlucky and the vaccine played no role.

Twitter wouldn’t have done this for a nothing burger article. They are telling us this article could hurt the false narrative. Therefore, you’ll want to share the article widely:

BELL’S PALSY AND RAMSAY HUNT SYNDROME

Is Gavin Newsom is out of sight likely because he has Bell's Palsy from his booster shot?

Update: Gavin Newsom is lying about his vaccine injury and now I can prove it

Gov. Newsom Injured by Moderna Booster Shot, Source Tells The Defender

Two Australian politicians had Bells a few months ago - Victor Dominello was diagnosed with Bell’s Palsy after concerning Covid-19 press conference

They say he has personal issues to attend to... like half his face is paralyzed. It's likely vaccine-induced Bell's Palsy or Guillain-Barre syndrome. That's why NO ONE is allowed to SEE him. Get it?

It’s been rumored that Gavin Newsom is out of sight since getting his booster because he developed Bell’s Palsy or Guillain-Barre Syndrome (GBS). This normally would happen within hours after getting his booster so this make perfect sense.

This also explains why nobody has seen him in public since Oct 27: anyone who saw him would instantly know.

I checked into this and I’m over 90% sure that this is true (but I can’t tell you publicly about it without revealing my source) which prompted me to write this article.

Am I 100% certain? No. This is just my personal educated guess piecing together the information (both from public and private sources) that I’ve gathered.

What’s your best guess?

How Steve Kirsch arrived at my hypothesis

Here’s the background for my hypothesis:
  1. Twitter reports of facial paralysis: first thought is Bell’s Palsy
  2. Emails with my friends say it is GBS
  3. Neurologist says either can cause facial paralysis
  4. Email I sent to a good friend of Newsom (who for sure knows his condition) about vaccine-induced Bell’s Palsy drew an immediate response asking for more info on effective treatments
Albert Benavides (aka WelcomeTheEagle88) recently did a VAERS analysis for me looking at symptoms that are elevated by the vaccine versus a 5-year baseline rate (VAERS reports from 2015-2019).

Look at what popped up on #11 (the 11th highest elevated adverse event). You are 1,533 times more likely to get Bell’s Palsy after the COVID vaccines than any other vaccine.

Vaccine side effects

NOTE: This screen shot is the “tip of the iceberg” as far as serious adverse events caused by the COVID vaccines. The full list is over 5,000 elevated adverse events and I’ll be writing about this later today on substack (subscribe to be notified).

Guillain-Barre after these vaccines is less likely than Bell’s Palsy by a factor of 4.5, so I’m guessing it is more likely Bell’s Palsy (but it could be GBS).

Did the vaccine cause Bell’s Palsy (or GBS) for Newsom? He was perfectly fine before the shot and within hours after the shot, he’s paralyzed. Could be bad luck. But come on.

Why doesn’t he just admit the truth, that he got Bell’s Palsy (or GBS) from the vaccine? Well, truth-telling is not how it is done in politics. The reason he won’t tell the truth it:

It would create vaccine hesitancy because it would be an admission that the vaccines aren’t safe like he claims

It would make him look silly for mandating these very dangerous vaccines that are killing/disabling adults and kids in California.

He doesn’t want to make the CDC look incompetent for never spotting the safety signal.

Newsom is still mandating your kids get the vaccine. A number of them will suffer neurological damage just like he did as a result of his mandate.
Bell’s and GBS are just two of over 5,000 adverse events that are elevated by these vaccine. More troubling is that the risk-benefit analysis for 5 to 11 I’ve seen shows we will kill 117 kids to maybe save 1 kid from COVID.

Governor Newsom and the CDC don’t seem to care about that; there’s not even a CDC category for vaccine deaths.

Over 120,000 Americans have suffered from Bell’s Palsy after vaccination (you take the incidence rate from the table and multiply by the minimum VAERS underreporting factor (URF) of 41 which is calculated here) and it could easily be over 250,000 cases.

A neurologist I know has over 2,000 clients with vaccine injuries (out of a 20,000 client base). The neurologist never had any events before now in his/her practice caused by the vaccine. This shows you it is the vaccine causing the events, not “over-reporting” as is claimed by the FDA.

When will it end?

I hope soon. But nobody in America likes to admit they were wrong. Even after they’ve been injured.

Joel Kallman, the creator of the V-safe application, died shortly after he was vaccinated. He never got a chance to tell people what he thought of the safety of the vaccine.

Let’s hope that Newsom gets the chance to learn from this and change his thinking.

P.S. If you think you know whether it is GBS or Bell’s Palsy, please comment below.

Wall Street Is Finally Paying Attention to the ‘Trust the Science’ Fraud

Blackrock’s Edward Dowd reveals how Big Pharma is going to become the next potential financial crisis. 

As Pfizer try to ‘pump their stock’ Hedge Fund guru Dowd, takes us inside what he calls the third great fraud in his lifetime, in this new bombshell interview with Dr Naomi Wolf.

Will CDC's Rochelle Walensky be found guilty of fraud?  She is testifying before a grand jury.

If you found this video informative I would suggested watching this video of Edward Dowd. Pfizer, FDA Hid Failed Clinical Trials Data, Says BlackRock Advisor

trust the science fraud

1,300 COVID vaccine-related injury claims are now pending before an obscure government tribunal

tribunal vs court
If you want to follow these cases and others please subscribe to this Subreddit "Tribunals" (Just Banned) 

Federal tribunals in the United States are those tribunals established by the federal government of the United States for the purpose of resolving disputes involving or arising under federal laws, including questions about the constitutionality of such laws.

Tribunals are often confused with courts. Tribunals are a part of the administrative system whereas courts, in general, are the creation of the judiciary which is entirely a separate organ. Both the courts and tribunals operate independently of each other. Although their objectives are the same yet there are major differences that establish them as separate bodies.

Tribunals are established under administrative law, which is an offshoot of decentralization of government authorities. Decentralization has resulted in the increased number of departments that have maximized the responsibility of government. Hence, these departments are given the authority to look after their disputes independently without any interference of courts except when the decisions are challenged in their legality.

Just like any court, a tribunal has a permanent establishment. There’s a bench of adjudicators who are responsible to pronounce a just and fair decision in favor of the aggrieved party. As compared to a court, the proceedings of a tribunal are less formal and speedy. The courts are expected to be rigid in their functions because they’re directed to do so as per the rules and code of conduct. Their performance is reported to the higher courts that initiate misconduct proceedings in absence of obedience to proper conduct. In tribunals, the adjudicators are selected from the organization or the department itself. The department makes its own sets of rules and they’re relatively flexible and informal.

The tribunal decisions are binding upon the parties. However, they’re appealable or challengeable in the court, provided the law under which the tribunal is established provides for the opportunity of appeal to the higher courts.

Reuters Story

As the Biden administration puts the final touches on an emergency COVID-19 vaccine mandate for companies with 100 or more employees, a crucial piece seems to be missing for the unlucky few who experience serious side effects: meaningful legal recourse.

More than 1,300 COVID vaccine-related injury claims are now pending before an obscure government tribunal, which to date has decided only two such cases, one involving swelling of the tongue and throat following the jab, the other alleging long-lasting, severe shoulder pain.

In both instances, the government, which requires claimants to prove their injuries are “the direct result” of a COVID-19 vaccine, denied compensation.

It’s a steep burden of proof. Lawyers tell me the vaccine is so new that there’s virtually no definitive research on injury causation to cite.  THIS IS A BLATANT LIE BY REUTERS. 

All you have to do is look at the Vaers database and see these stories about side effects

Indeed, the overwhelming majority of all litigants under what's known as the Countermeasures Injury Compensation Program have not succeeded. According to program data, 29 claims have been paid for injuries stemming from other vaccines since the tribunal’s inception in 2010. (Ten additional claims won approval but no compensation.) The other 455 claims – 92% – were denied or otherwise deemed ineligible for review.

For those who prevailed, the median award was $5,677, according to my calculations, spanning from a low of $31 to a high of $2.3 million, for a person who contracted Guillain-Barre Syndrome after receiving the H1N1 influenza vaccine.

There is no provision for damages based on pain and suffering.

For people like Jessica McFadden, who said she developed life-threatening blood clots after receiving Johnson & Johnson’s COVID-19 vaccine in April, legal options are unclear. She's not optimistic about her odds of recovering her losses, and it's certain she won't be able to recover any pain and suffering damages under the Countermeasures Injury Compensation Program.

McFadden, 44, said she was previously healthy and needed two emergency surgeries to remove massive clots in her lungs, heart and left leg. She spent nine days in the hospital, racking up $489,153 in medical bills, she said. Her insurance will cover most, but not all of the tab, she said, and she estimates she'll pay up to $7,000 out of pocket.

She emailed me a photo of extracted clots, which she said were removed during an agonizing procedure performed while she was conscious. They are thick and ropy, like nightcrawlers on a surgical tray.

McFadden, who said she has returned to work but is still taking blood thinners, has not spoken publicly of her ordeal until now. “I’m not an anti-vaxxer. I understand the need for the vaccine,” she said. “I was just trying to do the right thing.”

To be clear, an experience like McFadden described is extremely rare. The Centers for Disease Control and Prevention in May said that out of 8.7 million people who had gotten the J&J jab, only 28 suffered the complication known as thrombosis with thrombocytopenia syndrome. Per the CDC, there is a "plausible causal association" between the vaccine and the blood clots.

Johnson & Johnson in a statement said, “The safety and well-being of the people who use our products is our number one priority.”

To McFadden, the issue is not that COVID-19 vaccines are bad or that no one should get them. Rather, she said, what’s important is how we care for people “when something catastrophic happens” as a result, especially now that vaccine mandates are becoming so widespread.

For decades, vaccine makers have been shielded from product liability lawsuits thanks to the National Childhood Vaccine Injury Act of 1986. The law was passed after pharmaceutical companies were hit with lawsuits over a brain injury known as pertussis vaccine encephalopathy and threatened to quit making the DPT (diphtheria, pertussis and tetanus) vaccine altogether.

Under the 1986 law, people who claim to have been injured by DPT, hepatitis, influenza and other common shots bring their cases in a special, no-fault tribunal, the Vaccine Injury Compensation Program, known colloquially as “vaccine court.” Payouts (including attorneys’ fees) are funded by a 75-cent tax per vaccine.

The forum is far from perfect, but over the years, it has awarded more than $4 billion to injured claimants.

But that’s not where the COVID-19 vaccine injury cases are being decided.

In March 2020, then-Health and Human Services secretary Alex Azar issued a declaration under the Public Readiness and Emergency Preparedness (PREP) Act of 2005 providing liability immunity for medical countermeasures related to the novel coronavirus. Injury claims would be handled by the Countermeasures Injury Compensation Program, which is run by the Health Resources and Services Administration and is geared toward public health emergencies.

Coverage for claimants is limited: Lost wages up to $50,000 a year and out-of-pocket medical expenses. If the person died,

his or her next-of-kin can seek death benefits up to $370,376.

A spokeswoman for HRSA declined my request for an interview but explained in an email how the process works.

First, the person claiming an injury submits a request for a benefits form and relevant medical records. For COVID-19 vaccine injuries, the claims already include a veritable Merck Manual of maladies, everything from dizziness to deafness to death, according to HRSA data.

The form is “reviewed by CICP medical staff,” who decide whether the requester is eligible for program benefits.

If requesters don’t like the decision, they can ask for reconsideration by “a qualified panel, independent of the program.” The panel makes a recommendation to the associate administrator of the Health Systems Bureau of HRSA, whose decision on the payout is final.

You might notice a few things are missing, like an independent judge, a chance to present one's case in person, damages for pain and suffering and the right to appeal beyond the agency.

Vaccine court has all these features. CICP has none.

But this is where the COVID-19 vaccine cases are relegated, at least for now. Per the steps laid out in the 1986 vaccine law, for the COVID-19 vaccine to move to vaccine court, the CDC must first recommend the shots for routine administration to children. Then Congress must pass a law adding the 75-cent tax on each COVID-19 vaccine given, and the Secretary of Health and Human Services must move the vaccines to the Vaccine Injury Compensation Program.

All of this could take years.

Legislation is pending in Congress that would expedite the process (as well as upping vaccine court damages, extending the statute of limitations from three years to five and adding more special masters), but it has yet to gain traction.

Spokespeople for the bill’s sponsors in the House of Representatives – Texas Democrat Lloyd Doggett, and Republicans Fred Upton of Michigan and Mike Kelly of Pennsylvania – did not respond to requests for comment.

In the meantime, people like McFadden face a strict one-year deadline from the date of vaccination to file a claim with the CICP. But it’s not clear if filing in the CICP would preclude her from later moving her case to vaccine court, should that become an option.

She told me that she's waiting until early next year to decide how to proceed.

Healthy mom suffers cascade of health problems after COVID shot, vows to fight medical corruption

5,000+ People in The United States Have Had A Similar ADE Issue According To The NIH.

She is holding a rally and vigil on the steps of the Supreme Court on November 2nd for similar victims. 

A young mother, Brianne Driessen, was eager to sign up for the Astrazeneca COVID shot trial. Almost immediately after getting the injenction, she began experiencing severe adverse reactions, which continue to this day. In this interview with LifeSite’s Jim Hale, Driessen makes a passionate appeal for true informed consent and help for the thousands of fellow victims of the COVID jab.

A young mother from Utah shared with LifeSiteNews her nightmarish experience of developing severe adverse reactions immediately after receiving the COVID jab as part of the AstraZeneca COVID shot trial.

Brianne Dressen from Utah was a healthy mother of two young children and a pre-school teacher who eagerly signed up to the AstraZeneca COVID vaccine trial back in November 2020, as she was “confident that this was going to be our way out of the pandemic.” She received a first dose of the AstraZeneca vaccine on November 4 and started experiencing adverse effects within an hour of getting the shot.

Dressen first experienced tingling in her arm, blurred vision, hyper-sensitivity to sound, light and touch, dizziness, nausea, and leg numbness. Weeks later, she was admitted to the hospital after her legs “stopped working” and she became incontinent. She had to undergo intense physical therapy, including re-learning how to walk.

Dressen was later diagnosed with a number of serious health conditions which affect her nervous system. She shared her ordeal with LifeSiteNews correspondent Jim Hale.

After a first of “many visits to the emergency room” ruled out multiple sclerosis and other major neuro-degenerative disorders, Dressen was sent home where she had to stay in a room by herself because of her extreme sensitivity to sound.

“My sensitivity to sound was so severe that even my little girl’s voice was too much for my ears,” she recalled.

She also suffered from hypersensitivity to light and had to “put towels on the windows to make the room completely black.”

Dressen lost 20 pounds, as she suffered from nausea and vomiting, and experienced difficulties swallowing her food.

She said she was certain that the vaccine was responsible for her condition.

“There is no question in my mind that the vaccine caused this reaction,” she said, before expressing anger and frustration at the fact that AstraZeneca did not investigate her case thoroughly, as would be expected during a clinical trial.

“You would hope that there would be someone who would be appropriately tracking the data, that these cases (even if they’re rare) are evaluated, that they are discussed, that the information is disclosed in a full and transparent manner. Unfortunately, that has not been the case,” she said.

“I really wish I could say that the drug companies did their due diligence with this, but they didn’t,” she added.

Dressen also revealed that her case was not included in the list of severe adverse events that was published by AstraZeneca. “And now there’s their published clinical trial data. I’m not in it,” she said.

AstraZeneca claims to follow up with all serious adverse events cases for up to 720 days but monitored Dressen over a much shorter period of time.

“I definitely was a serious adverse event,” said Dressen, “I was followed up with for 60 days.”

The pharmaceutical giant also agreed in their contract with clinical trial volunteers to pay for any injury or medical need that would result from the vaccine. An agreement that they did not honor in Dressen’s case.

“After months of repeated pleading and fighting with them to help us with the massive pile of medical bills, I have 590 dollars from them.”

For a long time, doctors could not figure out what was wrong with the young mother. They first diagnosed Dressen with “anxiety” from the COVID vaccine. But she was then able to go to the National Institutes of Health (NIH) where she received appropriate diagnoses, which included a number of nervous disorders such as: non-length-dependent neuropathy, short-term memory loss, sensory neuropathy, dysautonomia and severe postural tachycardia syndrome.

The young woman still suffers from these adverse effects to this day, almost a year after having been vaccinated, and her life has not been the same since.

“My body went from functioning at a normal, healthy level; I was able to take care of my kids and my work, too,” she said. “Now, my big accomplishment today will be talking to you and the fact that I made myself breakfast.”

LifeSiteNews correspondent Jim Hale then asked Dressen to discuss how this event changed her views on the pharmaceutical industry.

“This has been very eye opening for me,” replied Dressen, “I feel like I’ve been plucked out of the matrix.”

Dressen explained that she grew increasingly distrustful of government agencies as she witnessed evidence of them purposefully withholding information from the public.

“These [adverse] reactions are not being disclosed to the public,” she said. “Because of this, the public is not being provided informed consent, but also the medical community is not being informed appropriately that these reactions can happen.”

Dressen also claimed that attempts at withholding information on adverse events from the public does not only come from social media platforms but also from within the medical world.

“There’s medical censorship happening,” she said, “there’s censorship with the research; we have researchers that have tried to get case studies published in scientific journals and they can’t get them published.”

The young mother became emotional when she recalled that some of the people suffering from these adverse effects have committed suicide.

“I had to write a eulogy for a dear friend of mine, for her husband to read after she took her life,” she said.

Dressen and Hale then discussed other cases of people that have suffered loss as a result of the vaccine’s adverse effects, including that of Ernest Ramirez, a father from Texas who recently lost his 15-year-old son to the Pfizer vaccine. Hale also mentioned that in a recent interview with LifeSiteNews, Dr. Robert Malone, a pioneer of the mRNA technology used in the development of the COVID vaccines “told us, flat out, if you have an adolescent son, he should not be getting the vaccine.”

Among some of the initiatives taken in response to this issue, Dressen mentioned a website with over 500 testimonies and accounts of people who have suffered from COVID vaccine adverse events.

Additionally, she announced that a press conference is going to take place on November 2 on the steps of the Supreme Court to hold government agencies accountable.

“We’re uniting with those like Ernest Ramirez and we’re going to the capital to plead with our elected officials to help us and to hold these agencies, the FDA, the CDC, the NIH, accountable, because we know acutely just how much they know,” she said.

“They know about the suicides [and] the suicide attempts, they know about people losing their jobs because of inappropriate mandates, they know about the sick kids, they know about people being buried under medical debt and losing their homes, they know about the issues with the clinical trials,” she added.

In conclusion of the interview, Dressen insisted that she was not anti-vaccine and explained that her husband had gotten the COVID vaccine, but she advocated for informed consent and not coercing people.

“I really believe that everybody should have appropriate full informed consent so they can make an appropriate choice for themselves; and also, because there is a risk, there absolutely needs to be a choice,” she said.

She condemned government agencies for letting people who suffer from these adverse events deal with them on their own and for abandoning them.

“The problem is, if you get a vaccine reaction like this, you are completely on your own. The government agencies are not going to help you,” she said. “You will not be able to get financially compensated and your medical teams will have no idea what to do with you.”


Brianne Driessen

Dr. Bryan Ardis Exposes Hospital Protocols Murdering Americans

Dr. Bryan Ardis discusses the 4,000 new cases of "multi-inflammatory disease"  among children where organs are getting inflamed and this is brand new in 2020. 


Donate and support our work: https://earthnewspaper.com/index.php/donate

The Dr. Ardis Show: https://www.thedrardisshow.com

Dr. Reiner Fuellmich: https://www.fuellmich.com


Dr. Bryan Ardis joins John Di Lemme on the CBJ Real News Podcast Show to discuss Covid-19 hospital protocols that are killing Americans, the deadly vaccine, and more!

Follow John Di Lemme and the CBJ Real News on Telegram at https://t.me/cbjrealnews

Support Conservative Business Owners and Entrepreneurs by going to https://ConservativeMarketplace.com/



Dr. Bryan Ardis hospitals are killing people

60 Minutes - 1967 Swine Flu Neurological Disorders Comparison

Good, honest, old-fashioned reporting. Those days are largely gone now.

This is an old segment from CBS '60 Minutes' on the swine flu (also known as H1N1) & the vaccine that was developed to stop the pandemic. 

The CDC pushed the swine flu vaccine in 1976 after several cases were reported but none were confirmed.  Watch below . . . 


Dr. Michael Hattwick  raised the flag about the potential links but it was ignored. Michael Hattwick, who ran the CDC's flu tracking center at the time, says while much of it was done looks unnecessary, in hindsight, at the time, it seemed courageous.  Dr. MICHAEL HATTWICK: There was always the fear of doing too little. I think this time, there'll be more fear about doing too much and that may be a lesson we learned from '76.



Vaccines For Kids Potentially More Dangerous than Virus, German Gov’t Reports

Germany Study

According to a safety report published by the Federal Institute for Vaccines and Biomedicines in Germany, the number of reported cases of suspected adverse effects following COVID-19 vaccination in children aged 12 to 17 has now exceeded the total number of COVID-related hospitalizations for children within the same age group since the beginning of the pandemic.

The report, which was published on September 20 by the PEI (Paul-Ehrlich-Institut), a German federal agency and medical regulatory body in charge of promoting drug and vaccine safety, has released new data on COVID-19 vaccines adverse effects, particularly among children aged 12 to 17.

The data, which was collected from the beginning of the vaccination campaign until August 31, shows that 1,228 vaccinated children aged 12 to 17 reported one or several suspected adverse effects following vaccination. This comes only three months after the beginning of the vaccination campaign for that age group, and just two weeks following a recommendation by the STIKO, the German Standing Committee on Vaccination.

By comparison, the total number of children aged 12 to 17 who were admitted to the hospital for COVID-19 between March 2020 and July 2021 is 1,225. In other words, within just 3 months, the number of cases of vaccinated children suffering from potential vaccine-related adverse effects exceeded the number of COVID-related hospitalizations within the same age group over a period of 16 months.

This new data seems to indicate that more children are suffering from the vaccine meant to protect them from COVID-19, than from the virus itself.

The most serious adverse effects reported include heart diseases such as myocarditis and pericarditis, as well as other serious health conditions such as thrombosis, pulmonary embolism, and the Guillain-Barré Syndrome.

Even more concerning are the first reported cases of fatalities following vaccination in that age-group. According to the PEI report, “three of the 1,228 reported cases of adverse effect have resulted in the death of the patients within two to twenty-four days following vaccination with [Pfizer/BioNTech].”

Based on the newly release data, if the vaccination campaign extends to all minors aged 12 to 17, as well as to other age groups, as is currently expected, the total number of vaccine-related deaths among minors could be triple or even four times that of COVID-related deaths in the same age group throughout the whole pandemic. In other words, the vaccines offered to protect children from COVID are potentially more dangerous to children than the virus itself, according to an analysis published by Susan Bonath of RT DE.

The report also showed a significant increase of reported cases of adverse effects in adults, including a staggering increase in severe adverse reactions. Data collected throughout the month of August shows a 15-fold increase with skyrocketing numbers of severe reactions going from 1,094 to 15,122 in just one month. A steady increase in the number of vaccine-related deaths can also be observed.

According to Bonath’s analysis of the report, the total number of reported vaccine-related injuries and deaths over a span of seven months far exceeds that of all other vaccines together over a span of twenty years, from 2000 to 2020, with the number of long-term effects almost four times higher and the number of deaths more than three times higher.

This remarkable discrepancy was pointed out by RT DE editor Florian Warweg at a press conference with the Federal Ministry of Health on September 8. Warweg, who referred at the time to data which is no longer up to date, asked Andreas Deffner, spokesperson of the Federal Health Ministry:

Why Synthetic mRNA Shots Are Not Like Traditional Vaccines


There is a lot of incoming information from the government and the private sector promoting the vaccine. Recently, there has been a significant uptick in compulsory demands for taking the COVID vaccine. This forced vaccination approach has made many people start to question why this coordinated pressure campaign has increased with such ferocity.  

As a result of such one-sided information, people are increasingly skeptical. In this video below you can review the counter-position for why people do not want to take the vaccination shot.  I am not sure who produced it, but we are sharing it in an effort to provide balance.  The claims are well cited.


covid survival rate chart


Guillain-Barré Linked To COVID-19 Vaccines?

What is causign Guillain-Barré syndrome?

What is Guillain-Barré syndrome?  

Swine Flu Vaccines in 1976 Were Linked To Guillain-Barré Syndrome

Guillain-Barré occurs when the body’s own immune system attacks and injures the nerves outside of the spinal cord or brain – the peripheral nervous system. Most commonly, the injury involves the protective sheath, or myelin, that wraps nerves and is essential to nerve function.

Without the myelin sheath, signals that go through a nerve are slowed or lost, which causes the nerve to malfunction.

To diagnose Guillain-Barre Syndrome, neurologists perform a detailed neurological exam. Due to the nerve injury, patients often may have a loss of reflexes on examination. Doctors often need to perform a lumbar puncture, otherwise known as a spinal tap, to sample spinal fluid and look for signs of inflammation and abnormal antibodies.

Studies have shown that giving patients an infusion of antibodies derived from donated blood or plasma exchange – a process that cleans patients’ blood of harmful antibodies - can speed up recovery. A very small subset of patients may need these therapies long-term.

What is causign Guillain-Barré syndrome?

The FDA reports that 12.5 million doses of the Johnson & Johnson vaccine have been administered — about 8% of the population of fully vaccinated people in the United States. As of July 13, 2021 (the day the FDA issued its warning), 100 cases of Guillain-Barré had been reported in individuals who received that vaccine. Of those cases, 95 were considered serious and required hospitalization; one case resulted in death.  

GBS symptoms usually develop within two days and start in the extremities

Symptoms of GBS typically develop within 42 days of vaccination, and the first symptom is often numbness or tingling in your hands or feet.

“The typical progression of GBS is from the legs up to the arms over a one-week to four-week period,” Dr. Levin says. “That can be accompanied by progressive heaviness and weakness in the legs the arms — and later on, there can be difficulty with swallowing and breathing, but those are unlikely to be initial presentations.”

Although the Johnson & Johnson shot is the only COVID-19 vaccine that has been linked to Guillain-Barré syndrome, it’s not the first time a vaccine has been linked to the disorder.

In rare cases, people have developed GBS after receiving the flu shot — about one case of GBS for every 1 million influenza vaccines administered. But why?

“There’s evidence that GBS is an autoimmune reaction in which the body produces antibodies directed toward myelin, the insulation of the nerves,” Dr. Levin explains. “Vaccines tend to rev up your immune system, which could rev up antibodies that recognize different tissues within your body as foreign — even though, of course, they are not foreign.”

It’s worth noting that, aside from the flu vaccine, there’s currently no conclusive association between GBS and other vaccines, though it hasn’t been ruled out, either.

Other symptoms of GBS may include:

Back pain.

Muscle weakness.

Heart rate or blood pressure problems.

Bell’s Palsy Linked To Covid Vaccines?

Bell’s Palsy side effects after vaccine

During the phase III Pfizer-BioNTech and Moderna trials, seven cases of facial paralysis or Bell's palsy were reported in the vaccine groups (7 of 35,654), and one case was seen in the placebo groups (1 of 35,611). A causal relationship was not established, but the FDA recommended that vaccine recipients be monitored.

Following the documentation of a case of Bell's palsy associated with vaccination,1 we were contacted by patients and colleagues from Canada, Australia, Europe, the UK, and United Arab Emirates. Questions raised were whether mRNA vaccine recipients are at increased risk of developing Bell's palsy, and what to recommend to individuals with a history of Bell's palsy.

It is unclear whether the vaccine caused the outbreaks of Bell’s palsy, but Dr. Paul Offit, a member of the FDA’s Vaccines Advisory Committee who voted to approve the Pfizer preventative, said in an interview with CNBC that the condition should be monitored. “I’m not dismissing that yet,” he said.

Despite geographical and seasonal variations, generally agreed incidence of Bell's palsy is 15–30 cases each year per 100 000 population. Ozonoff and colleagues rightly state that the predicted 12-month (annual) incidence of Bell's palsy inferred from mRNA vaccine trials is higher than that reported during the 2-month observation period of these studies. They concluded that the observed incidence of Bell's palsy in the mRNA vaccine arms was 3·5 to seven times higher than expected in the general population. However, safety data were collected for participants with a median follow-up of 2 months after the second dose; therefore, the data refer to an overall observation period of approximately 12 weeks from dose one. Given this, and considering Bell's palsy as the possible outcome of individual doses, the observed incidence in the mRNA vaccine trials would be roughly 1·5 to three times higher than in the general population 

The numerical imbalance reported with mRNA vaccine trials was not seen in the Oxford-AstraZeneca and Johnson & Johnson phase 3 studies using more traditional virus-based technology. Examination of adverse event data from the Yellow Card scheme in the UK and from the EU EudraVigilance database might help clarify this matter. As of March 21, the Yellow Card-reported frequency of facial paralysis or paresis and facial nerve disorder after any dose was close to 23 per million with the Pfizer-BioNTech vaccine and 13 per million with the Oxford-AstraZeneca vaccine. Excluding reports of facial paralysis cross-listed with a cerebrovascular accident, EudraVigilance data indicate a much higher frequency of facial paralysis after the Pfizer-BioNTech vaccine than after the Oxford-AstraZeneca vaccine (497 vs 56 cases or 13·6 vs 4·1 per million doses as of April 3). The risk of developing facial paralysis could be two to three times higher in individuals receiving mRNA vaccines than in those receiving traditional vaccines. These findings should be considered when selecting a vaccine for patients with a history of Bell's palsy.

People who have previously had GBS may receive a COVID-19 vaccine. To date, no cases of GBS have been reported following vaccination in participants in the mRNA COVID-19 vaccine clinical trials. One case of GBS was reported in a vaccinated participant in the Johnson & Johnson Janssen COVID-19 Vaccine clinical trial (compared to one GBS case among those who received placebo). With few exceptions, the independent Advisory Committee on Immunization Practices (ACIP) general best practice guidelines for immunization do not include a history of GBS as a precaution to vaccination with other vaccines.

People who have previously had Bell’s palsy may receive a COVID-19 vaccine. Cases of Bell’s palsy were reported following vaccination in participants in the COVID-19 vaccine clinical trials. However, the Food and Drug Administration (FDA) does not consider these to be more than the rate expected in the general population. They have not concluded these cases were caused by vaccination.

Why COVID-19 Vaccine Science Should Not Be Rushed

In 1976, an outbreak of the swine flu, influenza A virus subtype H1N1 at Fort Dix, New Jersey caused a mass vaccination of Americans. After the program began, the vaccine was associated with an increase in reports of Guillain-Barré Syndrome, which can cause paralysis, respiratory arrest, and death. This is the story of how in 1976, the US government faked a pandemic.

In January 1976, several soldiers at Fort Dix complained of a respiratory illness diagnosed as influenza. The next month, Private David Lewis, who had the symptoms, participated in a five-mile forced march, collapsed and died.

The New Jersey Department of Health tested samples from the Fort Dix soldiers. While the majority of samples were of the more common A Victoria flu strain, two were not. The atypical samples were sent to the Centers for Disease Control in Atlanta, Georgia, which found evidence of swine influenza A related to the 1918 flu pandemic, which killed 50 to 100 million people worldwide.

The Center for Disease Control (now the Centers for Disease Control and Prevention) verified the findings and informed both the World Health Organization and the state of New Jersey. On February 13, CDC Director David Sencer completed a memo calling for mass vaccination for the swine flu.

The CDC Assistant Director for Programs of the Center for Disease Control, Bruce Dull, held a press conference on February 19 to discuss the flu outbreak at Fort Dix and, in response to questions from reporters, mentioned the relationship of the flu strain to the 1918 outbreak.

US President Gerald Ford was officially informed of the outbreak memo on March 15 and the suggested vaccination program. He met with a “blue ribbon” panel that included Jonas Salk and Albert Sabin. Ford then made a televised announcement in support of the mass vaccination program.

A hearing was held before the United States Senate Appropriations Subcommittee on Labor, Health and Human Services, Education, and Related Agencies, and C. Joseph Stetler, a drug company spokesman, requested government indemnity for the vaccine manufacturers.

Pharmaceutical companies Sharp & Dohme (Merck & Co.), Merrell, Wyeth, and Parke-Davis also refused to sell doses to the government unless they were guaranteed a profit, a concession that the government also eventually made.

The House Appropriations Committee reported out a special appropriations bill, including $135 million for the swine flu vaccination program, which was approved on April 5. Two days later, the World Health Organization held a conference to discuss the implications of a swine flu outbreak for poorer nations.

On April 8, an official from the Federal Insurance Company informed Merck & Co., a manufacturer of the swine flu vaccine, that it would exclude indemnity on Merck’s product liability for the swine flu vaccine on July 1, 1976.

T. Lawrence Jones, president of the American Insurance Association, informed the Office of Management and Budget that the insurance industry would not cover liability for the vaccine unless the government extended liability protection.

The chairman of Merck wrote a memo a day later, April 13, to various government agencies, including the White House emphasizing the “duty to warn”. In May, other vaccine manufacturers including Marion Merrell Dow, Parke-Davis, and Wyeth, were notified of indemnity problems by their respective insurers.

Assistant Secretary Theodore Cooper (HEW) informed the White House on June 2 that indemnity legislation would be needed to secure Merrell’s cooperation. In June, other vaccine manufacturers requested the same legislation. A little more than two weeks later, the Ford administration submitted a proposal to Congress that offered indemnity to vaccine manufacturers.

Bruce Dull stated at a flu conference on July 1 that there were no parallels between the 1918 flu pandemic and the current situation.

Later that month, J. Anthony Morris, a researcher in the Food and Drug Administration’s Bureau of Biologics (BoB), was dismissed for insubordination and went public with findings that cast doubt on the safety of the vaccine, which was produced in fertilised hen’s eggs.

Three days later, several manufacturers announced that they had ceased production of the vaccine. Later that month, investigations into alleged swine flu outbreaks in other parts of the world found no cases of the strain. On July 23, the President sent a letter that urged Congress to take action on indemnification.

In early August, an outbreak of illness in Philadelphia was thought to be related to swine flu. It was later found to be an atypical pneumonia that is now called Legionnaires’ disease. On August 6, Ford held a press conference and urged Congress to take action on the indemnification legislation. Four days later, both houses of Congress passed the legislation.

Merrill became the first company to submit samples to the FDA’s Bureau of Biologics for safety testing, which approved it on September 2. Merck made the first shipment of vaccines to state health departments by September 22. The first swine flu inoculations were given at the Indiana State Fair.

In October, three people died of heart attacks after they had received the vaccine at the same Pittsburgh clinic, which sparked an investigation and the recall of that batch of vaccine.

The investigation showed that the deaths were not related to the vaccination. The President and his family received their vaccinations before the television cameras. On November 2, Ford lost the presidential election to Jimmy Carter.

Also in early November, Albert Sabin published a New York Times editorial, “Washington and the Flu.” He agreed with the decision to create the vaccine and to be prepared for an outbreak but criticized the “scare tactics” that had been used by Washington to achieve that. He suggested to stockpile the vaccine and to have a wait-and-see strategy.

By 15 December, cases of Guillain-Barré syndrome (GBS) affecting vaccinated patients were reported in 10 states, including Minnesota, Maryland, and Alabama. Three more cases of Guillain-Barré were reported in early December, and the investigation into cases of it spread to eleven states.

On December 16, a one-month suspension of the vaccination program was announced by Sencer. William Foege of the CDC estimated that the incidence of GBS was four times higher in vaccinated people than in those not receiving the swine flu vaccine.

Ford told reporters that he agreed with the suspension, but he defended the decision to create the vaccination program. Joseph A. Califano, Jr., was sworn in as Secretary of Health, Education, and Welfare on January 20, 1977. On February 4, Sencer was informed that he would be replaced as the head of the CDC. The vaccination program was not reinstated.

Laurence Gostin, in his article “At Law: Swine Flu Vaccine: What Is Fair?”, wrote that “the swine flu affair fails to tell us whether, in the face of scientific uncertainty, it is better to err on the side of caution or aggressive intervention.”

There is not even complete agreement about the causal relationship between the swine flu vaccine and Guillain-Barré syndrome, as noted in Gina Kolata’s book Flu: The Story of the Great Influenza Pandemic of 1918 and the Search for the Virus That Caused It.

She wrote that the CDC did not have a “specific set of tests and symptoms to define Guillain-Barré” and that since doctors who reported cases already knew that a link was suspected, a bias in reporting was introduced. She quoted Keiji Fukuda: “if a new virus gets identified or reappears, you don’t want to jump the gun and assume a pandemic is happening.”

See related articles: 

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Swine Flu Vaccines in 1976 Were Linked To Guillain-Barré Syndrome

Swine Flu Vaccines in 1976 Were Linked To Guillain-Barré Syndrome

Guillain-Barré syndrome is thought to be caused by a problem with the immune system, the body's natural defense against illness and infection. New neurologic symptoms is one of the reasons they stopped the J&J vaccines

Normally the immune system attacks any germs that get into the body. But in people with Guillain-Barré syndrome, something goes wrong and it mistakenly attacks the nerves.

This damages the nerves and stops signals from the brain traveling along with them properly, which can cause problems such as numbness, weakness and pain in the limbs.

It's not clear exactly why this happens. The condition is not passed from person to person and is not inherited.

In the past, the flu vaccine used in the US during a swine flu outbreak in 1976 were linked to an increased risk of Guillain-Barré syndrome.

Guillain-Barré symptoms

But research has since found the chances of developing the condition after having a vaccination are extremely small.

For example, a study into the vaccine used during the 2009 swine flu outbreak found that for every million people who had the vaccination, there were fewer than 2 extra cases of Guillain-Barré syndrome.

And evidence suggests that you are far more likely to get Guillain-Barré syndrome from an infection, such as the flu, than the vaccine designed to prevent the infection, such as the flu jab.

Guillain-Barré syndrome (GBS) is a rare disorder where the body’s immune system damages nerve cells, causing muscle weakness and sometimes paralysis. While its cause is not fully understood, the syndrome often follows infection with a virus or bacteria. Each year in the United States, an estimated 3,000 to 6,000 people develop GBS. Most people fully recover from GBS, but some have permanent nerve damage.

In 1976, there was a small increased risk of GBS after swine flu vaccination, which was a special flu vaccine for a potential pandemic strain of flu virus. The National Academy of Medicine, formerly known as the Institute of Medicine, conducted a scientific review of this issue in 2003 and found that people who received the 1976 swine flu vaccine had an increased risk for developing GBS. The increased risk was approximately one additional case of GBS for every 100,000 people who got the swine flu vaccine. Scientists have several theories about the cause, but the exact reason for this link remains unknown.

There have been several studies of the risk of GBS after flu vaccine and CDC monitors for GBS during each flu season. The data on an association between seasonal influenza vaccine and GBS have been variable from season to season. When there has been an increased risk, it has consistently been in the range of 1-2 additional GBS cases per million flu vaccine doses administered.

Studies suggest that it is more likely that a person will get GBS after getting the flu than after vaccination. It is important to keep in mind that severe illness and death are associated with flu, and getting vaccinated is the best way to prevent flu infection and its complications.

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