Archive for the ‘Activism’ Category

2007 Blast From the Past: “Faith in Quick Test Leads to Epidemic That Wasn’t”

https://www.nytimes.com/2007/01/22/health/22whoop.html

Credit…Jon Gilbert Fox for The New York Times

Dr. Brooke Herndon, an internist at Dartmouth-Hitchcock Medical Center, could not stop coughing. For two weeks starting in mid-April last year, she coughed, seemingly nonstop, followed by another week when she coughed sporadically, annoying, she said, everyone who worked with her.

Before long, Dr. Kathryn Kirkland, an infectious disease specialist at Dartmouth, had a chilling thought: Could she be seeing the start of a whooping cough epidemic? By late April, other health care workers at the hospital were coughing, and severe, intractable coughing is a whooping cough hallmark. And if it was whooping cough, the epidemic had to be contained immediately because the disease could be deadly to babies in the hospital and could lead to pneumonia in the frail and vulnerable adult patients there.

It was the start of a bizarre episode at the medical center: the story of the epidemic that wasn’t.  (See link for article)

__________________

**Comment**

Testing fiascos are part and parcel of the CDC’s MO.

For more:

The Problem with CDC Death Statistics

Recently, there’s been interest in the fact Lyme/MSIDS is horribly underreported, and with how deaths are recorded. This subject has resulted bill S.677A currently in the Assembly requiring coroners, pathologists, and medical examiners to report promptly to the local or superintending health department whether a deceased person at the time of death was afflicted with Lyme or any other tick-borne disease.

We’ve been told ad nauseam by our public ‘authorities’ that Lyme doesn’t kill people, yet it clearly does. A Wisconsin Lyme advocate keeps a memorial on her website of deaths linked to tick-borne illness. And, there’s a lot of them!

What is written on death certificates is very important as it directly affects how a disease is perceived.  A disease causing many deaths will be taken more seriously and will have more research funding allotted for it. We are seeing this play out with COVID-19 and the fact hospitals were paid to count deaths as COVID, even when there were confounding issues and many times COVID wasn’t even the direct cause. Then there’s the issue of faulty PCR testing for COVID which is positive for nearly everyone, which further casts doubt on the validity of COVID mortality statistics.  Yet, these inflated numbers are being used daily to drive a message that COVID is extremely deadly, despite the fact experts continue to say the mortality rate for COVID is nearly the same as the seasonal flu.

While all deaths are important, the CDC has inflated COVID deaths but has a long history of deflating Lyme/MSIDS deaths.

Recently, there’s been a call for an investigation into the CDC’s COVID ‘data disaster’:  https://madisonarealymesupportgroup.com/2021/02/15/data-disaster-call-for-a-cdc-investigation-free-online-event-feb-17-2021/  If you missed it but still want to view it, go here.

The following article sheds light on cause of death reporting:

https://healthimpactnews.com/2018/death-certificate-clerk-reveals-how-cause-of-death-reporting-is-subjective-and-cdc-statistics-not-reliable-when-making-public-health-decisions/

Death Certificate Clerk Reveals How Cause of Death Reporting is Subjective and CDC Statistics are Not Reliable When Making Public Health Decisions

This is a closeup view of the Death certificate

Comments by Brian Shilhavy
Editor, Health Impact News

Feb. 20, 2018

In our recently published article on Sudden Infant Death Syndrome (SIDS) we referenced how the Centers for Disease Control and Prevention (CDC) and the World Health Organization (WHO) list 130 official ways for an infant to die according to official categories of death, but adverse reactions to vaccines is not one of them.

Joy Fritz is a Death Certificate Clerk, and she recently published some of her observations in the field of death recording on Facebook.

Joy relates how she and her husband were concerned about the severity of the flu season as was being reported in the media, and that she “started reading the FDA package inserts for different flu immunization options to get informed on which immunizations might be safest for our <1 year old and 6 year old.”

She states that she wanted to make an informed decision for her family, and that

“What I ultimately wanted to compare was the risk of death.”

She learned that public records on influenza deaths stated that there were no deaths related to adverse reactions to flu medications or flu shots.

However, being in the field of death recording, she dug deeper, and has presented her research and experience to the public.

She writes:

Our current system for capturing mortality rates can and does provide a mostly uninvestigated and inaccurate picture of what causes a death. The process for creating and registering causes of death for public records is a complicated, convoluted, politicized, completely open to both ignorance and the manipulations of personal, professional, and governmental interests.

I’m the one creating these statistics and I offer you this: If you take one thing away from this, take away a healthier skepticism about even the most accepted mainstream, nationally reported, CDC or other ‘scientific’ statistics.

A Humbling Exposé into the Creation of Mortality Rates and its Impact on Our Public Health Beliefs and Choices

by Joy Fritz
Facebook

I work with doctors, coroners and the local county registrars everyday to create death records. It’s what I do for a living and wanted to share my thoughts on the mortality rates being thrown around on main stream and social media regarding the influenza epidemic. Please note: This information I am sharing is not limited to influenza reporting, but rather, serves as a case study of how the mortality rate recording system (mal)functions at large.

I am sorry to say that death rates are NOT as simple nor as valid as every news broadcaster with perfectly-trained vocal delivery makes them sound, and they are absolutely not the infallible pillar of medical history as the CDC purports.

Our current system for capturing mortality rates can and does provide a mostly uninvestigated and inaccurate picture of what causes a death. The process for creating and registering causes of death for public records is a complicated, convoluted, politicized, completely open to both ignorance and the manipulations of personal, professional, and governmental interests.

I have come to realize how greatly this reality becomes a public health issue during this past flu season when every major media outlet is providing us with live updates on the accruing death toll. Seeing these reports caused me concern for my family.

My husband and I discussed what preventative treatment we might consider. I started reading the FDA package inserts for different flu immunization options to get informed on which immunizations might be safest for our <1 year old and 6 year old. What I ultimately wanted to compare was the risk of death.

My kids getting sick is just part of life, other people getting sick is just part of life, lowering the risk of death to my family and the people around me is what I cared about when it came specifically to the seasonal flu.

I started researching mortality rates to find the line item in the CDC reports for deaths due to influenza vs adverse reaction to influenza medications and immunizations.

I found influenza rates, no problem.

Flu medications and shots? No deaths reported. Awesome. What a simple decision to make.

But, being in the mortuary industry and curious how they get these reports, I looked at the last full report for 2014 and dug deeper and found that they simply code and reorganize the data that they receive from death records. The death records that I am typing up and registering everyday.

So my head started exploding. And I felt, and still feel, sick. I have realized that without knowing it, I knew exactly how influenza deaths are recorded, and I know exactly why there is no line item in the CDC’s mortality rates for adverse reactions to common medical treatments.

Before I continue, please know that I will not be explaining all the ins and outs of my job, nor the incredibly rare reality that medication complications and adverse reactions do get captured (usually in box 112 of the death record, not as the primary underlying cause).

Those exceptions are made possible by exceptional, and likely, very principled people, choosing individually to go above and beyond the call of protocol, whether that be the family that is aware of the impact of the legal documentation that occurs after death and stays level-headed and involved mere hours after the death of their loved one, or an insanely humble and honest doctor, in conjunction with the coroner medical-legal officer that trusts and cooperates with the honest doctor and vigilant family to think outside the box of their standard procedures.

Almost 5 years and nearly 5,000 death certificates later, I can say with confidence that that kind of post-death communication concoction is at a statistical percentage point that even the CDC would consider insignificant.

So, in the spirit of very uncomfortable truthfulness I will share a snapshot of the core issues embedded in the daily procedures of creating the death statistics that we so desperately need to make prudent health decisions for ourselves and our families. I will also include some examples of how these core issues would manifest into faulty statistical analysis at the level of our public health and lead to the miscalculation of the benefits and risks surrounding our individual medical choices.

Core Issue A: Doctors that provide causes have not all been trained the same way, and therefore do not provide standardized responses.

This may at first glance seem minor, as it always has to me, but this directly affects the cause that the doctor lists on the death certificate.

Some doctors prefer providing the underlying cause of death as something that has happened immediately in the last days or weeks before death such as pneumonia or influenza, and leave out the more chronic illnesses. Other doctors decide they will provide the more long-standing health conditions as the cause of death such as diabetes, asthma and congenital abnormality while leaving out the more immediate illnesses.

Some doctors include both the short term and long term diagnoses. This has to do with many factors such as in what capacity the doctor saw the patient -hospital vs hospice care for example- or the immediate availability of the complete medical record within the time frame being impressed by the mortuary due to upcoming funeral or cremation services. Or, simply due to the way the doctor personally prioritizes information.

Again, way too many factors to go into here, but the basic issue of the lack of standardization in cause of death diagnosis and reporting remains.

In this case the same patient can have all these conditions: influenza, pneumonia, diabetes, asthma and congenital abnormality on his/her medical record simultaneously and any one of those conditions listed are correct and valid and could be entered as a stand alone cause and be registered by me and the local and state registrars offices without a query.

It’s the doctor’s preference and his medical opinion – yet the national attention given, medical research dollars, and yearly health choices we all make are swayed by which ever cause this particular doctor, with his/her own particular training and personality decides to jot down on the worksheet and send back to me to enter into the official record.

CORE ISSUE B: What most people don’t know is that doctors are not allowed to attest to anything that is not a strictly NATURAL cause of death.

Falls, medication complications or overdoses, causes with the word ‘injury’ in it, anything that is considered an unnatural or external cause is outside the realm of their jurisdiction as far as the death record is concerned.

The Coroner would need to be contacted and agree to certify or co-certify a death record that has an unnatural or external cause listed.

This is a whole other, very complicated reporting issue that I will not get into in this post.

I will say, however, from perspective of a mortuary representative, that everyone involved (doctor, coroner, registrar and myself) understands that the delay caused by any coroner involvement is highly dreaded and avoided if at all possible due to the amplified grief it can cause the family if they do not want an autopsy or investigation done or have to suffer a delay in services and or an upset in their own personal closure process.

However, the majority of doctors are aware of their own limitation to certify only natural causes of death. And usually in the interest of serving the grieving family, will provide the simplest natural cause that they know will quickly pass the approval of the local registrar’s office, fulfill their duty as a signing physician, and enable the grieving family to move forward with their scheduled burial or cremation services.

It should be noted here that doctors are under an additional pressure since they have a limited time set out by their State Health and Safety Codes to provide causes of death to a funeral home.

In California it is within 15 hours of death, although that is rarely achieved. Delays of more than a few days after death would risk them getting their license reported to the the state medical board for lack of compliance.

What works about this system? The system is created in such a way that naturally occurring infectious disease (such as influenza) CAN and is being reported and recorded in national mortality rates. However, the lack of standardization in the way doctors report it creates an unreliable number to set as the threshold for what constitutes an epidemic.

What does NOT work about this system? It does not report on the true consequential timeline of the patient’s medical treatment, including unnatural and external complications and errors in their medical care and is therefore woefully inadequate to make ANY medical claims or recommendations.

The first example to illustrate the impact of this issue is as follows:

I read a post from a nurse the other day that shared her story of being hospitalized due to complications of the flu. Even though she had gotten the flu shot every year, she had only gotten influenza this year. Five days after experiencing flu symptoms she went into her medical provider and was prescribed Tamiflu.

She went through her course of medication. Her flu symptoms eased but she started getting a tightness in the chest, which further worsened until she needed to be hospitalized for pneumonia and a close call with sepsis.

The conclusion of her post -and her medical opinion as a nurse – was that this year’s flu was very dangerous and anyone less healthy than her could have easily died with her symptoms, so she urged everyone to please get the flu shot to prevent the flu from spreading.

The saddest part about reading her story was discovering that she must not have read the Tamiflu manufacturer’s insert, which states that:

“No influenza vaccine interaction study has been conducted” and “Efficacy of TAMIFLU in patients who begin treatment after 40 hours of symptoms has not been established” and furthermore, “Events reported more frequently in subjects receiving TAMIFLU compared to subjects receiving placebo in prophylaxis studies, and more commonly than in treatment studies, were aches and pains, rhinorrhea, dyspepsia and upper respiratory tract infections.”(emphasis added)

This would lead to an alternate, very feasible medical conclusion that her hospitalization and pneumonia was the result of using a medication that has not been tested on a population of her vaccination status and symptoms duration, which also has the adverse reaction of a URTI.

But what if it wasn’t her? What if someone less healthy than herself with her exact symptoms and medication course HAD died?

Her medical opinion, and many other medical care providers opinion would have been that it was influenza that had caused the death, instead of the complications of the medication.

In the medical provider’s mind, the likelihood of influenza causing the death is greater than the medication causing the death because of mortality rates – but they are the ones creating the mortality rates – so what is considered reasonable likelihood is being created in a closed loop. A regurgitating cycle.

So, whether the attending physician at the hospital was aware of this medical misstep by the other medical provider or not, in this case the hospital physician could simply put ‘Influenza’ on the causes of death worksheet and send it back to me. Influenza would be entered in the death record and be reported in the state and then national database as such with no question from me or the government registrars.

What this has created, then, is a serious public health reporting conundrum. Death due to complications of improperly prescribed medication are NOT being calculated into the national reporting agencies in a real-time setting.

Neither would they be communicated in real-time to the public. Instead the public would simply hear of the rising influenza death toll and run for more medication (and likely not be reading the manufacturer’s insert either to verify if they truly are a good candidate for that medication).

In this medication example, as you can imagine, even IF they realize that the medication was prescribed erroneously, it would not be in the professional best interest of the medical provider or medical facility to report this prescription error and it’s possibly fatal complications to the family or public health officials.

I have many friends and family in the medical industry and it is easily admitted that legal and personal liability is a factor in the considerations of proper reporting.

However, if and when this possibly fatal prescription misstep was ever reported it would be in some very passive EMR analysis many months or years later, with no urgency or real-time public health warning. The ability for government to cross-check and minutely examine nearly 3 million decedent medical records of varying electronic availability – annually – it’s just not there.

This failed mechanism in the mortality rate ‘generator,’ if you will, is the same for the hotly debated adverse vaccine reactions. This is the reason you see horrible adverse vaccine reactions and deaths being claimed by parents on social media, but no item line for them in national statistics.

It is not because they don’t exist or don’t happen. The real-time data reporting system of death recording is not set up to calculate these deaths.

For the families that become aware of the adverse reactions in time to request investigation (<24 hours after death), and are able to request any relevant pathological specimens to be procured before the burial or cremation of their loved one, would then need to have the time and resources to go through the lengthy reporting and court procedures through VAERS.

A very few families do, and if they can establish enough scientific evidence (like pathology reports), find and produce enough experts and professional support, they MIGHT eventually get the causes of death amended and compensation for their loss paid out by the allotted government fund. And after 5, 10, 15 or 20 years, this passive data capture system might accrue enough statistical information to be reported back to the medical community so that they adjust their recommendations.

So, just like in the medication example, any death due to an adverse reaction to the flu shot or for ANY regularly scheduled wellness immunization, would similarly not be captured in the standard process of death recording.

As before, the doctor can still provide either influenza or any other natural occurring immune response as the only cause of death. He would send it to me and I would enter it in, get the state to approve it, and ‘Viola!’ – a thoroughly inaccurate mortality rate reporting.

In Conclusion

One of the most difficult realities for me to recognize in examining the mortality rate reporting system that I am a part of, is that the medical community itself is suffering from the ignorance that this kind of circular mortality rate generating system creates. Doctors and coroners are limited by the already existing mortality rates to gauge the likelihood of what caused death.

That kind of system can only regurgitate the same causes of death over and over again by forcing its reporters to use the same types of ‘acceptable’ death diagnoses as what ALREADY exists.

And these are the statistics the medical community uses to educate themselves and provide informed consent to the patient on what the most prudent option is for medical care to safeguard health and prevent death.

And, yes, I will take the opportunity here to say that we can logically apply this critical analysis of the lack of proper data capture to those reluctant to vaccinate or use medications.

There is no current national data capture system that records the morbidity or mortality rates of those who chose less medical intervention or choose to not vaccinate themselves or their kids. We don’t know what their life expectancy, quality of life or mortality rate is in our modern day, with the advancements in hygiene, technology and post-disease-diagnosis medical care availability being considered. It could absolutely be worse, statistically, but we wouldn’t know.

For nationally reported statistics we are left then with bad data on one side, and no control group data on the other. Hardly the recipe for safe or settled scientifically guided medical care.

Now where does that leave you and me? Our highly subjective yet somehow infallible weaponry of mortality rates – whether from national statistics or the social media horror stories – has us and all our friends and family swinging the manic flag of ‘People are dying!’

This flu season for example, some of our friends are saying ‘People are dying from flu! Get vaccinated! Take medication!’ or other friends are saying ‘People are dying from adverse reactions to medications/shots! Don’t get vaccinated! Drink elderberry!’

And we are all running for the nearest remedies that we are sure will help us – why? Because of statistics – OR because we don’t see statistics reflecting our lived reality, so we do the best we can to discern our health without statistics.

But I’m the one creating these statistics and I offer you this: If you take one thing away from this, take away a healthier skepticism about even the most accepted mainstream, nationally reported, CDC or other ‘scientific’ statistics.

Humans who had no concept of their national impact made them. The numbers are not hard – they are very, very fluid. And conversely, have a healthier skepticism about all the alternative remedies we welcome as hopeful scientific-ish options. There is no unbiased, century long, data capture system set up for these choices either.

As a parent, the most painful part of taking a step back and looking at all this, is having to humbly admit – I don’t know what the right thing to do is.

I don’t have the unbiased data I need to make the safest decision for my children.

I don’t know what the right thing to do is for myself, or for my husband.

I don’t know what side of the fence to stand on in the vaccination and mainstream medicine battlefield, and I don’t want to stand on a side: I just want the unbiased, uncorrupted and standardized data needed to accurately assess the benefits vs. the ultimate risks for my family’s health.

In the face of this fallible data capture system, my own resolution that I am willing to publicly recommend – no matter what medical choices you decide is best – would be for us all to become self reporters. Keep a health journal for each family member complete with dates and times and severity of symptoms of illness and track dates and dosages of any medical treatment administered.

Track degree of fevers, severity of migraines, frequency of ear infections, changes of behavior, hospitalizations, medications dosages and immunization combinations etc.

Think critically and ask questions when you see inconsistencies in any health recommendations offered to you or your family. Request and encourage a satisfactory discussion of benefits and risks with your medical provider.

Download and thoroughly read the manufacturers insert provided on the FDA’s website for any medication or immunization you are considering and verify that you are a good candidate for that medication.

If you decide to use that medical treatment, record any minor reactions in the health journal and immediately report any somewhat severe reactions to your medical provider and ask for that information to be added to your electronic medical record so that it might inform any future medical provider on your individual contraindications you may have in other medication courses.

Remember that each of us is liable for our own health choices, you cannot expect a medical provider to be a perfect assessor of what’s best for you.

Follow up and make sure proper reporting was done on the medical provider’s part to the appropriate national databases, or report it yourself.

MedWatch reports for medications and VAERS reports for vaccines.

This recommendation is less for you and more for others and for the sake of having the appropriate authorities informed so they can eventually take medical treatments off the market and create the demand for safer ones.

Those kind of databases can only function well for the populations they serve if they are being used by everyone.

My Final Thought: Yes, people are dying. Everyday. I do their death records every flu season or surfing season.

And try as hard as we do – and no matter how absolutely shredded inside I am especially when I do an infant or child’s death certificate- we will never eradicate death.

We CAN work to slowly eradicate and reform bad systems and misinformation. And even though there is no immediate gratification in it, we will probably save more lives when we work intelligently, truthfully and ethically towards a better future. And that usually starts with a lot of humility and admitting that change is needed.

If anyone has ideas, would like to share their thoughts or their own expertise for consideration, or somehow otherwise contribute to unifying this polarized health battlefield, feel free to add a comment.

Original Source.

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**Comment**

Once again, you can’t count something you aren’t tracking.  If it doesn’t have a code, it doesn’t exist in the eyes of our public ‘authorities.’  It becomes circular reasoning – or an infinity loop containing only the data they perceive as important.

I agree with the author – be skeptical about anything coming from the CDC.  They tell you what they want you to know.

The reason autopsies aren’t performed on Lyme/MSIDS patients is because we’ve been told nobody’s dying from it, yet autopsies are precisely what we need.

Pathologist: FDA ‘Misled the Public’ on Pfizer Vaccine Efficacy & the Elderly Are Suddenly Dying

https://childrenshealthdefense.org/defender/fda-misled-public-pfizer-vaccine-efficacy/?

02/17/21

Pathologist: FDA ‘Misled the Public’ on Pfizer Vaccine Efficacy

In an amended reply to the FDA’s rejection of his concerns about Pfizer’s clinical trials, Dr. Sin Hang Lee says the FDA is glossing over potential risks of an mRNA vaccine while concealing its true efficacy.

Pfizer’s announcement in November 2020 that clinical trials showed its COVID-19 vaccine was “95% effective” prompted Dr. Sin Hang Lee, a Connecticut pathologist, to question Pfizer’s methodology and petition the U.S. Food and Drug Administration (FDA) to require accurate counts of COVID-19 cases in the Pfizer/BioNTech COVID-19mRNA vaccine trial before granting the vaccine Emergency Use Authorization (EAU).

As The Defender reported in November, Lee, who is director of Milford Molecular Diagnostics, said:

“Until an accurate count of COVID-19 cases in the vaccinated and placebo groups has been determined for vaccine efficacy evaluation, we are asking the FDA to stay its decision regarding the emergency use authorization for this vaccine.”

Lee’s request was rejected by the FDA on Dec. 11, the same day the agency approved Pfizer’s vaccine for emergency use. On Feb. 8, Lee filed an amended reply. 

Here’s the sequence of events as they unfolded:

On Nov. 23, 2020, Lee, along with Informed Consent Action Network(ICAN) and its counsel, submitted a Citizen Petition and petition for administrative stay of action to the FDA relating to the phase 3 trial of the BNT162b/Pfizer vaccine to prevent the novel coronavirus SARS-CoV-2. 

In the petition and stay, Lee requested the FDA amend the study design for the late-stage trial of Pfizer’s COVID-19 vaccine. Specifically, Lee requests:

“Before an EUA or unrestricted license is issued for the Pfizer vaccine, or for other vaccines for which PCR results are the primary evidence of infection, all “endpoints” or COVID-19 cases used to determine vaccine efficacy in the Phase 3 or 2/3 trials should have their infection status confirmed by Sanger sequencing, given the high cycle thresholds used in some trials. High cycle thresholds, or Ct values, in RT-qPCR test results have been widely acknowledged to lead to false positives … All RT-qPCR-positive test results used to categorize patient as “COVID-19 cases” and used to qualify the trial’s endpoints should be verified by Sanger sequencing to confirm that the tested samples in fact contain a unique SARS-CoV-2 genomic RNA.”

The petition makes these requests because the phase 2/3 clinical trial of the Pfizer COVID-19 vaccine uses a presumptive RT-qPCR (“PCR”) diagnostic test, which is known to generate high rates of false-positive results.

In addition, the Pfizer vaccine trial primarily uses a PCR test that employs cycle thresholds up to 44.9 to identify COVID-19 “cases” despite the fact that “positive” results that require cycle thresholds greater than 30 to 35 are usually false positives, according to Lee.

Lee offered to re-test the residues of tested samples in his laboratory if Pfizer is unable to do so in order to confirm Pfizer’s stated vaccine efficacy rate of 95%. 

Lee’s Sanger sequencing-based method for molecular diagnosis of SARS-CoV-2 was published in International Journal of Geriatrics and Rehabilitation.

On Dec. 11, 2020, the same day the FDA granted Pfizer Emergency Use Authorization for its COVID-19 vaccine, the FDA responded to Lee’s petition and request for stay.  The agency “conclude[d] that the petitions do not contain facts demonstrating any reasonable grounds for the requested action” and denied the petitions.

The FDA, among other things, stated that “PCR testing does not need to be followed by Sanger or other sequencing for purposes of clinical diagnosis. Currently, reverse real-time PCR (RT-PCR) tests can both amplify and confirm the identity of viral genetic material in a single reaction, without a separate sequencing step.”

On Feb. 8, Lee, through ICAN’s counsel, submitted a detailed and thoroughly cited reply to the FDA’s denial of his petition and stay. This reply points out the inaccuracies, contradictions and omissions in the FDA’s denial of the petition. 

Lee wrote that the FDA’s letter denying the petition and stay

“shows that the FDA has not conducted an adequate evaluation of the Pfizer vaccine’s efficacy, especially concerning issues about the accuracy of RT-qPCR testing of SARS-CoV-2 in clinical specimens.”

Lee’s detailed response, which can be read in full here, goes on to say:

“The FDA has misled the public. The key misleading statements are analyzed below point-by-point according to the sequence of their presentation in the Letter but under the following four categories for the convenience of the readers:

“A. Cherry-picking to eviscerate the guidance for issuance of an EUA for a COVID-19 vaccine.

B. Knowingly promoting inaccurate PCR tests for SARS-CoV-2.

C. Finding excuses for using PCR tests with high false-positive rates for this vaccine trial.

D. Glossing over potential risks of an mRNA vaccine while concealing its true efficacy.”

Lee, ICAN and others are weighing possible future actions.

_____________________

**Comment**

You may recognize Dr. Lee due to the following posts:

Dr. Sin Hang Lee is one of the true-blue researchers left who call a spade a spade.

https://www.naturalnews.com/2021-02-16-elderly-population-suddenly-dying-off-for-unexplained-reasons.html

Elderly population suddenly dying off for unexplained reasons, and it’s no longer coded as covid-19

Image: Elderly population suddenly dying off for unexplained reasons, and it’s no longer coded as covid-19

(Natural News) Around the world, medical authorities are seeing a spike in elderly deaths, after covid-19 vaccination. Gibraltar, a nation located at the southern tip of Spain, is suffering from an unexplained surge in elderly deaths. In the second week of January, a subset of the elderly population suddenly started to die off. The new wave of unexplained elderly deaths is occurring at nearly three times the magnitude of covid-19 deaths that were recorded during 2020.

The new, unexplained surge in elderly deaths is occurring approximately forty times faster when compared to the overall timeline of covid-19 deaths that occurred since a pandemic was first declared. This surge in elderly deaths occurred after 5,847 doses of experimental mRNA injections were administered to the citizens of Gibraltar. In just one week, 17 percent of the country’s population had been inoculated with the first dose of Pfizer’s mRNA experiment.

Before the vaccine experiment began, the covid-19 related death toll accounted for ten people. After the vaccine rollout, the total number of deaths had skyrocketed to forty-five people. In the first eight days of the vaccination program, thirty-five seniors suddenly passed away.  (See link for article)

___________________

**Comment**

But of course it is all being blamed on a new “covid-variant.”  Therefore more injections will be required.

Please read the updated list of deaths/adverse reactions:  https://madisonarealymesupportgroup.com/2020/12/21/warning-3150-injuries-in-1st-week-of-covid-vaccines-among-american-healthcare-workers-pregnant-women-included/

 

URGENT: Strike Down Law Removing Parents From a Child’s Healthcare

https://standforhealthfreedom.com/action/strike-down-the-dc-minor-consent-law/  Petition Here

Our Stand

  • One of the most egregious minor consent bills to ever surface in this country, B23-0171, became D.C. law on December 23, 2020. The measure, which received widespread opposition from advocates nationwide, makes it possible for 11 year olds to be vaccinated behind their parents’ backs. This dangerously misguided law includes provisions to ensure that parents never find out their child got vaccinated by requiring insurance companies, vaccine administrators and schools to conceal the vaccination(s) from parents. This effectively prevents parents from ever knowing their child’s complete medical history.
  • Medical and legal experts say the D.C. minor consent law is predatory, racist and destructive to children and families everywhere. That’s why we’re asking for your immediate help to overturn it! (Keep reading; helping is easy.)
  • Before the minor consent law goes into effect, it has to undergo a 30-day congressional review period per the District of Columbia Home Rule Act. The act makes it possible for Congress to overturn the law, although this has only been done successfully a handful of times in history. As such, we are urging all U.S. advocates to support a congressional resolution that’s been filed to strike down the D.C. minor consent law. If we don’t stop this bad law in our nation’s capital, it could easily become law in your state!
  • The D.C. minor consent law is a bad law. In addition to putting children in potential physical danger, it breaks multiple federal laws, instructs healthcare providers to engage in criminal misconduct by falsifying medical records, and targets disadvantaged inner-city minorities by paving the way for them to be “groomed” for medical interventions that their parents (and possibly even their own doctors) will never know about. Most of all, it erodes the parent-child relationship by interfering in a family’s personal matters and encouraging kids to keep secrets from their parents. This, experts say, lays the foundation for a relationship filled with fear, paranoia and mistrust. Allowing minor children to consent to vaccination is dangerous because children don’t have the emotional maturity or intellectual capacity to make important medical decisions. Additionally, by removing parents from their child’s healthcare decisions, it forces young pre-teens and teens to make complex choices without the advice or support of those who know and care for them best — their parents. 
  • The pharmaceutical industry and medical lobbying groups are hard at work redefining the parent-child relationship and influencing lawmakers and public officials to give ultimate healthcare decision-making authority to the state. However, there is no justification for the state to eliminate a parent’s legal and moral right to make an informed decision about vaccination on behalf of their minor child, especially when doctors and other vaccine providers have no liability or accountability for what happens to the child after vaccination.
  • The D.C. minor consent law needs to be overturned immediately! We are asking people from all over the country to take action NOW so that this predatory law in our nation’s capitol is abolished and won’t set precedent for other states to follow! Taking action is easy. Simply click below to send a pre-drafted (and customizable) email and tweet to your federal officials urging them to support the congressional resolution to strike down the D.C. minor consent bill! Remember: No one knows children like their parents do, and coming between families will have devastating, long-lasting effects — both physical and psychological.

Your home address information is required from the legislative offices to ensure you are reaching out to your designated representatives. Your email and your phone number are used to establish connection with your designated representatives. Messages from non-constituents don’t have the same impact on a legislator as messages from verified constituents, who can vote for that officeholder. We do not share your name and contact information with any third parties unless legally required to do so.

Have a question or need help?
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**Comment**
This is important for children everywhere, but particularly for vulnerable children with Lyme/MSIDS.
Since vaccines are not without risks and have directly caused death and severe adverse reactions, children need direction from their parents who are the most vested in their lives and health.  Not only that, but children being treated for tick-borne illness have complicated regimens that parents need to be completely privy to.  Blocking them from this process will yield nothing fruitful.
While proponents of this bill will state child abuse as a viable reason for this harmful bill, there are already laws protecting children.
Children are only children for a small window of time.  For those children desiring vaccination against their parents’ approval, they don’t have to wait long to be on their own to do what they want.  In the meantime, let parents do what they feel is best for their children.
This intrusion into family life and blocking of parental rights is growing due to states adopting the UN Rights of the Child in piecemeal fashion.  In short, it takes power away from parents and puts it in the hands of the government to decide what’s best for your child.  This would allow a judge or bureaucrat to make decisions – not you:  https://madisonarealymesupportgroup.com/2020/03/05/door-opened-for-international-law-to-override-parental-rights-in-u-s/

Lyme/MSIDS families are already fighting an uphill battle.  In many instances they are accused of child abuse: https://madisonarealymesupportgroup.com/2017/09/14/dutch-parents-accused-of-child-abuse-due-to-children-with-lyme-disease/

CAN YOU IMAGINE HOW MUCH WORSE IT WOULD GET?

If you are unfamiliar with the Parental Rights Amendment, please read:  https://madisonarealymesupportgroup.com/2017/04/20/why-we-need-the-parental-rights-amendment/

Also:  https://madisonarealymesupportgroup.com/2017/02/21/parental-rights-in-medical-settings/  Excerpt:

Right here in the U.S., the family of Justina Pelletier found that out the hard way in 2014 when the state of Massachusetts took Justina from them and placed her in the custody of Boston Children’s Hospital. Doctors there were free to enroll her in clinical trials (without parental consent) for the somatoform disorder diagnosis they had given her, rather than continuing the treatment for Mitochondrial disease that her parents and doctors at Tufts Medical Center had been following. After public outrage following her parents going public, Justina was finally returned to her parents 16 months later, in much worse condition than when she was taken away.Her story reemerged in 2016 as the family filed suit in federal court against the state and the hospital who so severely injured their daughter.

Isaiah Rider of Missouri was also taken by the state over a disagreement regarding his treatment. He was finally released by the state of Illinois who had been granted custody (though he was never a resident of the state until he went into foster care) when Lurie Children’s Hospital (Chicago) doctors decided they knew better than his mom. While in foster care, Rider suffered sexual assault. He was finally returned to the custody of his grandparents in his home state, but wasn’t fully released from Illinois care until June of 2016, months after his 18th birthday!

AS SAD AS IT SOUNDS, THOUGH, THE RIDERS AND THE PELLETIERS ARE THE LUCKY ONES.

Just so you know the abuse of power is happening right here in Wisconsin:  https://madisonarealymesupportgroup.com/2020/02/22/doctors-afraid-to-refer-injured-children-for-evaluations-fear-an-abuse-specialist-might-jump-to-the-wrong-conclusion/

To learn more:  https://parentalrights.org/get_involved/

Scientists Warn of Potential COVID Vaccine-Related ‘Ticking Time Bomb’

https://childrenshealthdefense.org/defender/potential-covid-vaccine-related-ticking-time-bomb/

02/11/2
Scientists Warn of Potential COVID Vaccine-Related ‘Ticking Time Bomb’
Studies suggest that COVID vaccines may trigger antibody-dependent enhancement in some people, a condition that could cause them to develop more severe symptoms when exposed to the wild virus than if they hadn’t been vaccinated.

Associate Professor of Health Sciences Adam MacNeil at Brock University, Canada and his Ph.D. student Jeremia Coish were among the earliest to warn, last June, of the dangers of not looking very carefully at the possibility that vaccines might trigger antibody-dependent enhancement(ADE) of disease. This could mean that people who are vaccinated might, paradoxically, suffer more severe disease when exposed to the wild virus than if they hadn’t been vaccinated.

In their aptly titled article, “Out of the frying pan and into the fire? Due diligence warranted for ADE in COVID-19,” published in the journal Microbes and Infection in June 2020, MacNeil and Coish argue that ADE is well known to be a risk for coronavirus-mediated infections, as well as dengue.

For those not already familiar with ADE, it is the paradoxical immune response that makes a person who was previously exposed to the disease, or a vaccine targeting it, more — not less — susceptible in the event that they’re subsequently infected.

Proceed with caution

Seemingly countering this view, in August 2020, was viral epidemiologist Leah Katzelnick Ph.D., a dengue and zika specialist now in the employ of the National Institute for Allergy and Infectious Diseases headed by Dr. Tony Fauci. Along with co-author Scott Halstead,. Katzelnick argued that ADE shouldn’t be something to be feared. Katzelnick and Halstead proposed that the fundamental differences between SARS-CoV-2 infection that can cause COVID-19 and other diseases, for which ADE has been shown, meant that ADE would be highly unlikely.

They supported their arguments with evidence from cases of classic, intrinsic ADE, notably infectious peritonitis, a coronavirus infection in cats, as well as from respiratory syncytial virus, dengue and SARS — suggesting significant differences in the pathology, epidemiology and immune responses involved in these diseases as compared with COVID and SARS-CoV-2 infection.

Careful readers of Halstead and Katzelnick’s paper will note that while the authors largely dismiss the ADE risk, they very clearly identify a risk of vaccine hypersensitivity (or VAH), a closely related immunological hyper-reaction that was first identified in the late 1960s when children developed atypical measles following measles vaccination.

Many who’ve used the paper to dismiss ADE risks may only have read the title and abstract and not picked up that Katzelnick and Halstead dismiss only intrinsic ADE or iADE (i.e. the risk of disease enhancement on re-infection in the absence of vaccination).

They also may not have read the sombre advisory in the paper’s last sentence:

“Given the magnitude of the repertoire of COVID-19 problems and the need for an effective vaccine, the full force of worldwide investigative resources should be directed at unravelling the pathogenesis of VAH.”

There is not much to suggest that this advisory has been heeded, other than the fact that thousands of volunteers have been put through Phase 3 trials and there has been no evidence of spikes in more severe reactions among those vaccinated with the real thing, as opposed to the placebo.

Herbert Virgin, Ann Arvin and colleagues, writing in Nature, one of the most influential journals in the world, made a not dissimilar call for caution back in July. These authors discuss the great difficulties in identifying the incidence and frequency of ADE (and VAH) and suggest that “… it will be essential to depend on careful analysis of safety in humans as immune interventions for COVID-19 move forward.”

Transparency is key

This requires full transparency of surveillance data so that cases of infection and reinfection post-vaccination can be correlated against severe reactions following infection or vaccination. It also requires time — much more time than we’ve had so far.

Presently, data released by VAERS (Vaccine Adverse Event Reporting System) in the U.S. and the MHRA (Medicines and Healthcare products Regulatory Agency) in the UK don’t come close to telling us anything about the ADE or VAH risk. In fact, there will have to be a lot more re-infection before we know conclusively one way or another. And will we be able to find out if there are genuine issues with ADE or VAH, or will the authorities manage to keep a lid on it by just not communicating them given many reactions will be substantially delayed following vaccination?

Timothy Cardozo from New York University and Ronald Veazy from Tulane University took it a step further in their article in the International Journal of Clinical Practice published in October, when Phase 3 trials for the COVID frontrunner vaccines were in full swing. They argued not only that vaccine-mediated ADE (i.e. VAH) risks were more than just theoretical, they also suggest that the risks may be greater following particular types of mutations in the circulating viruses.

In their discussion on SARS-CoV-2, they discuss how very tiny changes, such as changes in the conformity (shape) of its spike protein both before and after fusion with host cells, via ACE2 receptors might impact those who’ve been vaccinated. Several months on with emerging evidence that some variants are able to evade the immune response that has been trained to offer protection against the original Wuhan variants, there is cause for even greater concern. This risk also can’t be dismissed on the basis of the results of the Phase 3 trials

What Cardozo and Veazy also suggest is another point we’ve long been concerned about. That relates to the fact that trial subjects — let alone members of the public who’re now lining up for COVID vaccines — are just not being informed of these potential risks, and the delayed nature of possible ADE/VAH reactions.

What about vaccinees who become ill several months after being vaccinated, suffering the classic range of symptoms associated with many respiratory diseases (including COVID), such as fever, chills, cough, shortness of breath, headache, fatigue, and so on? Will they know that these symptoms might be related to enhanced COVID disease mediated by the vaccination given to them months before, something that didn’t occur to them because they thought the vaccine gave them protection from COVID?

Cardozo and Veazy then show how informed consent forms for volunteer subjects in vaccine trials fail to meet the required ethical standards for informed consent. While ADE is mentioned, it is generally added at the end of the list of possible risks and its implications and identification are unlikely to be adequately understood by the lay public.

With a tick in the box and a sense from regulators and vaccine makers that they’ve successfully negotiated the hurdle of ADE/VAH risks, there’s been no further discussion of the issue. The vast majority of pre-vaccinees lining up as part of the global mass vaccination roll out simply have no idea of the risk — because they’re not being told.

Could ADE be a ticking time bomb?

Does non-disclosure as part of the informed consent process constitute not only a breach of medical ethics, but also a breach of law? In our view, that’s highly likely and should evidence accrue in the future, this will be something the courts will need to grapple with.

Presently there is no evidence of any significant ADE/VAH signal — but it is too early to tell and many cases could have gone undetected.

Is it possible that some instances of ‘long COVID’ could be a form of ADE? This is a possibility we have been considering. Typically people who get long COVID don’t test as positive from nasopharyngeal swab tests. But in deep seated systemic infections the mucosa may not show evidence of viral multiplication, whereas the infection may become systemic in certain tissues and be enhanced. This possibility cannot easily be dismissed.

Could the problem increase with new variants of SARS-CoV-2? Yes, as explained above.

What you can do:

  1. Anyone who is deciding to have the vaccine should inform themselves of the ADE and VAH risk, where there could be a considerable delay between vaccination and the experience of disease symptoms that may be more severe than those that would occur without the vaccine.
  2. Let those you know who are considering or planning to have the COVID vaccine of this risk. Read and share our article, “Informed consent — is this fundamental right being respected?“
  3. Share this article widely.

Originally published by Alliance for Natural Health International.

The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children’s Health Defense.

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**Comment**

Could this be ADE/VAH?

For more deaths and serious adverse reactions (including deafness, blindness, myocarditis, paralysis, and much more):

https://madisonarealymesupportgroup.com/2020/12/21/warning-3150-injuries-in-1st-week-of-covid-vaccines-among-american-healthcare-workers-pregnant-women-included/