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Injecting Babies: 1986 v Today

Important reminder regarding the explosive growth in the vaccine schedule since 1986

Injecting Freedom by Aaron Siri | August 7, 2024

If you have not seen this before, please take a moment to really let this image we created sink in—and keep in mind that this only reflects the vaccines given during pregnancy and the first year of life (there are far more thereafter on the current schedule):

Also keep in mind that virtually every single one of today’s vaccines was developed by a pharma company knowing it would not face liability for injuries caused by these products. This is because, as most of you know, the National Childhood Vaccine Injury Act of 1986 gave them immunity from having to pay for harms.

And chronic childhood diseases, many of which are autoimmune or immune-mediated, have exploded from 12.4% in the early 1980s to over 50 percent of children today. CDC and public “health” authorities cannot figure out the cause despite desperately searching (though they haven’t studied vaccines, even though smaller independent studies have indicated vaccines are a major contributor).

With that in mind, let this chart also sink in, comparing the clinical trials relied upon to license Pfizer’s top five selling products (excluding the COVID-19 vaccine) with vaccines given in the first six months of life:

For a more in-depth treatment, read my written testimony to Congress.

August 10, 2024 Posted by | Science and Pseudo-Science | | Leave a comment

Judges Back Meta in Vaccine “Misinformation” Battle, Free Speech Advocates Vow to Fight On

By Dan Frieth | Reclaim The Net | August 10, 2024

The 9th Circuit US Court of Appeals ruled this week in favor of Meta, Facebook’s parent company. The case was brought forward by the Children’s Health Defense (CHD) over allegations that the social media giant violated free speech rights.

The lawsuit, initiated in August 2020 and later updated in December, claimed that Facebook, along with its CEO Mark Zuckerberg and two fact-checking entities, Science Feedback, and the Poynter Institute’s PolitiFact site, was complicit in an unconstitutional act of privately exercising governmental censorship. CHD alleges that Facebook, in collaboration with the Centers for Disease Control and Prevention (CDC) and other federal institutions, is censoring content and discussions that the government is barred from suppressing under the First Amendment.

We obtained a copy of the opinion for you here.

The plaintiff specifically accused these sides of working in tandem to unfairly stifle valid attempts to discuss vaccine safety on Facebook, often through indirect yet sensorial measures like the use of warning labels. According to CHD, this type of arrangement between public entities and private corporations represents a breach of the First Amendment due to its perceived status as “state action.”

Despite these arguments, the 9th Circuit court concluded that CHD was not successful in meeting the initial requirement for state action, as the censorship inflicted was more a result of Meta’s content moderation policies and not any directive under federal law. Further, the court also asserted that CHD did not present any evidence of a binding agreement requiring Facebook to execute any particular action in response to misinformation about vaccines.

Although all judges did not share the same opinion, Circuit Judge Daniel P. Collins presented a partially dissenting viewpoint. He opined that the interactions between Meta and the Government involving the suppression of specific types of vaccine-related speech were substantial enough to evoke First Amendment considerations.

Expressing disappointment and worry, CHD CEO Mary Holland stated, “If we cannot stop the government’s joint action with Big Tech to censor unwanted information, our First Amendment is a pyrrhic victory — it means almost nothing in our real world of social media.” While she was pleased with the non-unanimous nature of the decision, Holland hinted at the possibility of appealing to the US Supreme Court after further review.

At the heart of the court battle, ongoing for almost four years, were claims, primarily leveled by CHD’s then-Chairman and Chief Executive Counsel, Robert F. Kennedy Jr., that tactics employed by the US Government to pressure Facebook into censoring vaccine “misinformation” were existential threats.

August 10, 2024 Posted by | Civil Liberties, Full Spectrum Dominance, Science and Pseudo-Science | , , , | Leave a comment

JOHN OLIVER RECYCLES GARBAGE VACCINE MISINFORMATION

The HighWire with Del Bigtree | August 8, 2024

HBO funnyman and vaccine shill, John Oliver, made another attempt this week on his show to amplify the mainstream vaccine safety narrative, citing the same studies he referred to in a similar segment on his show in 2017. Del once again destroys his stale, recycled misinformation.

August 9, 2024 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular, Video | | Leave a comment

Be Careful What You Say

How honesty leads to the trauma of unnecessary psychiatric hospitalization

Involuntary Commitment and Forced Mental Health Treatment Violate Human Rights

By Dr. Roger McFillin | Radically Genuine | August 8, 2024

Picture a soul in turmoil, wrapped in the suffocating embrace of despair. In the sanctuary of a therapist’s office, they finally find the courage to voice the unspeakable:

“Sometimes, I think about not being here anymore.”

The words hang heavy in the air, a testament to the crushing weight of their pain, loneliness, and emptiness. This confession, born from a place of vulnerability and trust, should be the beginning of a deeper healing journey.

During these intense emotional struggles, it’s important to understand that thoughts of escape, including suicide, are a common human response to overwhelming pain. There’s a vast chasm between contemplating an end to suffering and actively planning to end one’s life.

Context is everything.

The mind, overwhelmed by anguish, may grasp at any perceived exit, including the idea of nonexistence. But voicing these thoughts doesn’t signal imminent danger. Rather, it’s often a cry for understanding, a desperate reach for connection in the depths of isolation.

Skilled and experienced therapists understand this.

The very act of sharing these dark musings with a trusted professional can be profoundly cathartic. It’s in these raw, unfiltered moments that true therapy has the potential to work its magic. A skilled therapist, one who can navigate these turbulent waters without succumbing to panic, becomes a lifeline. They offer not just a listening ear, but a steady hand to guide the patient through the storm, helping them to contextualize their pain and find hope in the midst of despair. This is the essence of healing – not in avoiding the darkness, but in facing it together, unafraid.

Fast forward to mental healthcare in 2024.

As the demand for mental health services skyrockets, we’re witnessing a disturbing trend: the proliferation of ill-equipped therapists flooding the market. What was once a skilled profession has, in many cases, devolved into little more than paid listening.

The rise of virtual therapy platforms, while increasing accessibility, has created a cohort of isolated practitioners. Lured by the promise of higher profits without the overhead of a physical office, many therapists now find themselves cut off from the vital support networks of supervisors and mentors. Without this crucial guidance, they’re left to navigate treacherous emotional waters alone, often defaulting to a “cover your ass” mentality when confronted with challenging situations.

Simultaneously, as large hospital networks muscle into the mental health arena, therapy is increasingly reduced to an appendage of psychiatry. The nuanced art of healing is replaced by a simplistic “take your pills and manage your mental illness” approach. This medicalization of human suffering is fundamentally dehumanizing, reducing complex emotional states to mere chemical imbalances.

The consequences of this shift are stark. Individuals brave enough to voice thoughts of death are no longer met with understanding, but with fear. Their pain is hastily labeled as emerging “mental illness,” triggering a rigid psychiatric protocol that leads to overmedicalization and unnecessary hospitalization.

“I want you to go to the emergency room”

The knee-jerk mantra of risk-averse therapists and doctors who’ve been brainwashed to treat every fleeting suicidal thought like a ticking time bomb.

They herd the emotionally vulnerable into sterile, overpriced hospital rooms, mistaking cold fluorescent lights and paper gowns for actual care. It’s a convenient way to abdicate responsibility, slap a band-aid on deep-seated pain, and pad the pockets of our broken healthcare system – all while patting themselves on the back for “saving lives.”

A Rise In Psychiatric Hospitalizations

The U.S. mental health care system is at a breaking point, buckling under the weight of an insatiable demand for inpatient care. Recent federal data, as reported by CBS News, reveals a system in crisis: hospitals and clinics are operating at a staggering 144% capacity for inpatient psychiatric beds. This alarming statistic, courtesy of the Substance Abuse and Mental Health Services Administration (SAMHSA), exposes the raw nerve of a long-festering problem – a dire shortage of psychiatric inpatient facilities.

Yet, this begs a crucial question: Is this surge in demand a genuine need, or merely a symptom of a more insidious systemic failure?

The COVID-19 pandemic has cast a long shadow over youth mental health, with alarming consequences. A recent study comparing mental health emergency admissions among young people before and after the outbreak reveals a disturbing trend. In the two years following March 2020, youth psychiatric emergencies surged by an astonishing 116.7% compared to the same period in 2018-2020. Even more concerning, this new wave of patients skewed younger and were less likely to have prior psychiatric histories.

These findings suggest a troubling shift: the pandemic appears to have triggered new, earlier onset psychiatric manifestations in previously unaffected youth. Moreover, these emergencies lead to psychiatric drugs as a matter of course.

Which leads to worsening outcomes.

Primary Care Driving Hospitalizations

The mental health crisis among youth has been sensationalized to a dangerous degree, leading to misguided interventions that may do more harm than good. In pediatric offices across the country the use of quick, invalid screening measures that reduce complex emotional states to simple checkboxes is the primary assessment approach. These cursory assessments, administered by primary care doctors ill-equipped to handle nuanced mental health concerns, are causing undue panic.

A single checked box on these questionable screening measures can set off a chain reaction of fear-mongering, with parents being urgently directed to emergency rooms for what may be nothing more than typical teenage angst or temporary emotional struggles. This knee-jerk approach not only overwhelms emergency services unnecessarily but also risks pathologizing normal developmental experiences.

The media’s portrayal of primary care doctors drowning in a youth mental health crisis obscures a more insidious reality: these physicians, despite their best intentions, are conducting mental health evaluations in alarmingly short timeframes without the proper training to contextualize their findings.

The result is a perfect storm of misunderstanding, where the vulnerability and complex emotions inherent to adolescence are stripped of their context and hastily labeled as mental health emergencies. This approach not only fails to address the real needs of struggling youth but also potentially traumatizes families and clogs a healthcare system already stretched to its limits.

Even if these youth are not hospitalized they are going to placed on a drug that will at least double the risk of suicide, if not more. Lexapro is often prescribed despite the 6-fold increase in suicide risk!

The Trauma of Psychiatric Detention

When desperate parents drag a sullen teenager to the ER, or a vulnerable adult finds themselves cornered by an ER social worker, a grim dance begins. The fluorescent-lit stage is set for a performance of “crisis management theater,” where real human suffering collides with bureaucratic checklists and liability concerns.

Parents, gripped by fear that their child might take their own life, often feel coerced into consenting to psychiatric hospitalization and medication. This fear becomes a potent weapon wielded by hospital staff, despite the lack of evidence that such interventions actually prevent suicide.

Ironically, within academic circles, it’s widely acknowledged that these very interventions may increase the likelihood of suicide. This grim reality makes a perverse kind of sense: patients are prescribed powerful, mood-altering drugs and then discharged back into the very circumstances that initially drove them to contemplate suicide.

The experience of psychiatric detention is frequently described as traumatizing. Patients are stripped of their dignity – quite literally during invasive searches – and their autonomy, as their phones and personal belongings are confiscated. Many report being treated like cattle by burned-out, unprofessional staff.

Young women often feel unsafe, surrounded by men who are also experiencing mental health crises. For women struggling with the aftermath of sexual violence – a common precursor to psychiatric hospitalization – the hospital stay itself can be profoundly re-traumatizing.

This system, designed ostensibly to help, often inflicts further harm. It substitutes genuine care and understanding with a one-size-fits-all approach that prioritizes risk management over true healing. In our rush to “do something,” we’ve created a revolving door of trauma, where those seeking help often emerge more damaged than when they entered.

When parents, armed with knowledge and a desire to protect their children from potentially harmful interventions, attempt to resist the pressure to medicate, they’re often met with a dismissive and exasperated “What do you want us to do then?”

It exposes a mental health apparatus that has become reliant on the false promise of quick-fix pharmaceutical solutions, lacking the resources, training, or willingness to explore alternative approaches. This attitude effectively holds families hostage: either accept potentially harmful psychiatric drugs or be left with no support at all.

This false dichotomy – drugs or nothing – is a damning indictment of a system that has lost sight of its purpose. It reveals a profound lack of creativity and compassion in addressing mental health crises. Instead of working collaboratively with families to develop comprehensive, individualized care plans, hospital staff often default to a one-size-fits-all approach that prioritizes expediency over efficacy.

Moreover, this response subtly shifts blame onto the parents, implying that by refusing medication, they’re somehow obstructing their child’s care. It’s a manipulative tactic that exploits parental fear and guilt, further eroding trust between families and mental health providers.

Fear Based Therapy

The mental health industry has a dirty secret: it’s terrified of the patients it claims to help. Therapists, those supposed bastions of understanding and support, turn into protocol-driven robots at the mere whisper of suicide. Gone is the empathy, replaced by a checklist of CYA questions designed more to protect their licenses than to save lives.

This is how they are trained.

This fear-based charade masquerading as care has created a toxic environment where honesty is punished. Patients learn quickly: bare your soul at your own risk. Admit to dark thoughts, and watch your therapist’s eyes glaze over with panic as they mentally rehearse their mandatory reporting script.

In my years of specializing in treating chronically suicidal clients, I’ve witnessed firsthand the deep-seated trauma inflicted not just by their original experiences, but by the very system purporting to help them.

A disturbing pattern emerges, particularly among women survivors of sexual violence. Their acute trauma reactions are frequently misunderstood and hastily misdiagnosed as bipolar disorder or other psychiatric illnesses, leading to a cascade of inappropriate treatments and interventions. The psychiatric hospitalizations that often follow are not just ineffective; they’re actively traumatizing.

When these survivors finally find their way to my office, the damage is palpable. Trust, the very foundation of effective therapy, has been shattered by their previous encounters with mental health professionals. It can take months of patient, careful work to rebuild that trust, to convince them that it’s safe to be open and honest in therapy. This process is painstaking, requiring us to undo layers of iatrogenic harm – harm caused by the very institutions and individuals tasked with healing.

The tragedy here is twofold: not only are these women denied proper care for their actual traumas, but they’re also subjected to a secondary trauma at the hands of a mental health system that fails to recognize the complexities of their experiences. This cycle of misdiagnosis, inappropriate treatment, and subsequent re-traumatization doesn’t just delay healing – it actively impedes it, sometimes for years. Many never recover.

What Genuine Help Looks Like

True healing begins with the compassionate ear of a skilled, experienced therapist who can create a safe space for emotional expression and validation. This approach recognizes a fundamental truth: everything, including emotional pain and suicidal thinking, is temporary. By understanding struggles in their proper context, therapists can help clients navigate their darkest moments without resorting to extreme measures.

A competent therapist knows that most expressions of suicidal thoughts are not declarations of intent, but rather desperate attempts to communicate profound suffering. This nuance, while seemingly obvious, often eludes less experienced or inadequately trained professionals who are paralyzed by fear and uncertainty. Instead of reacting with panic, skilled therapists help clients explore their pain and envision a life worth living, even in the midst of emotional turmoil and trauma.

When someone is in emotional turmoil and suicidal risk is present, truly skilled therapists know that a gentle, personalized approach can make all the difference. Instead of rushing to hospitalization, these compassionate professionals take the time to really listen and understand. They work hand-in-hand with the person in crisis, crafting a safety plan that feels right and makes sense for their unique situation. It’s not about imposing rules, but about finding inner strength and support.

Effective therapy often involves teaching clients how to regulate intense emotions and tolerate distress. This might include techniques drawn from dialectical behavior therapy (DBT) or other evidence-based approaches. For many, additional support such as telephone coaching and family-based therapies can create a plan to weather crisis periods. These interventions recognize that suicidal crises tend to be episodic and often resolve when the underlying problems are addressed.

Primary care doctors should not be administering mental health screening measures or prescribing psychiatric drugs for complex emotional issues. Their well-intentioned but misguided interventions often exacerbate the situation, medicalizing normal human experiences and setting patients on a path of unnecessary and harmful treatments.

Working in “mental health” requires patience, understanding, and a willingness to sit with discomfort – both from the client and the therapist. By moving away from a fear-based, reactionary model of care towards one that embraces complexity and prioritizes genuine human connection, we can create a mental health system that truly serves those in need.

When the storm of the mind rages, feel-good therapy buzzwords and empty reassurances are as useful as a paper umbrella in a hurricane. What’s needed isn’t another degree or certification, but something far rarer: the guts to stare unflinchingly into the abyss of another’s pain without flinching. In the end, perhaps the most radical act in modern mental health care is simply having the backbone to shut up, sit down, and bear witness to suffering without trying to sanitize it.

August 8, 2024 Posted by | Science and Pseudo-Science, Timeless or most popular | Leave a comment

Pharma, WHO Team Up to Create Permanent ‘Pandemic’ Market for Mandated, Experimental Vaccines

By Brenda Baletti, Ph.D. | The Defender | August 6, 2024

Big Pharma and its key investors are rolling out a new strategy — “the full takeover of the public sector, specifically the World Health Organization (WHO), and the regulatory system that now holds the entire market hostage” — according to a new investigative report by Unlimited Hangout’s Max Jones.

What’s behind the new strategy? The pharmaceutical industry is facing a “patent cliff” by 2030, as many of its blockbuster drugs are set to lose their patent protection, placing $180 billion in sales at risk and threatening to topple the industry.

According to Jones, for years, when patents expired on profitable drugs, pharmaceutical giants deployed a “mergers and acquisitions” strategy, buying up smaller drug companies to add to their product portfolios.

As a result, the industry is now dominated by a handful of companies, conventional chemical drugs exist for most health issues, and the regulatory process for new ones has become onerous.

Big Pharma has now pivoted to acquiring biotech and biologic companies, whose products are “more complex, unpredictable and difficult and expensive to make,” than chemical-based medicine, Jones wrote.

Conventional drugs are chemically synthesized and have a known structure according to the U.S. Food and Drug Administration (FDA). Biologics come from living humans, animal or microorganism cells, and are technologically altered to target particular proteins or cells in the immune system. The FDA calls biologics “complex mixtures that are not easily identified or characterized.”

As a drug class, biologics offer an appealing solution to the patent cliff problem, because they can’t be easily replicated like generic versions of conventional drugs.

Instead, producers make “biosimilars,” which unlike genetics can’t simply be interchanged with the original drug during a course of treatment without serious safety risks, according to Jones. And while generics are cheap, biosimilars are still expensive to produce. There also are regulatory hurdles to getting biosimilars to market.

However, Jones wrote, the serious safety issues associated with biologics — the high risk of serious adverse events associated with the COVID-19 vaccine, for example — make it difficult for drugmakers to find commercial success in a conventional regulatory environment.

“Luckily for Big Pharma,” Jones wrote, the WHO and its private backers “are pursuing an unprecedented legal process that would cement loopholes that could solve these significant market challenges of at least some biotechnologies.”

Such loopholes made Pfizer and Moderna’s COVID-19 mRNA vaccines — the paradigmatic example of this new strategy — Big Pharma’s highest-selling annual market success ever.

Distribution of the COVID-19 vaccines to approximately 70% of people globally was possible only because of the “fast-tracked, deregulated development and mandated consumption of the experimental drugs,” Jones wrote.

The industry hopes to replicate that model with other drugs. And it has already begun — last month the Biomedical Advanced Research and Development Authority, or BARDA, gave Moderna $176 million to develop an mRNA bird flu vaccine.

Stakeholders behind the WHO have turned it into an arm of Big Pharma

According to Jones, the process of rapidly developed and mandated experimental drugs was first adopted by the U.S. military for bioweapons threats. Now, it is being internationally legitimized by the WHO through the agency’s revisions to the International Health Regulations (IHR) and its continued attempt to push its pandemic treaty.

The amendments were watered down and the treaty was partially thwarted at the last meeting of the World Health Assembly, which ended on June 1. However, the powers added to the amendments and the language in the treaty WHO and its backers are still hoping to advance next year show the type of biotech pandemic market Big Pharma has in the works.

According to Jones, this market:

“Will not be one that depends on the free will of consumers to opt in and out of products — but instead relies on tactics of forced consumption and manipulation of regulatory paradigms.

“At the forefront of this push are the WHO’s public-private-partners/private stakeholders, who directly shape and benefit from this policy. Their influence has, in effect, turned the WHO into an arm of Big Pharma, one so powerful that it already demonstrated its ability to morph the entire international regulatory process for the benefit of the pharmaceutical industry during the COVID-19 pandemic.”

These stakeholders can wield this power in part because the WHO receives 80% of its funding from private stakeholders.

Those stakeholders include private-sector giants like Bill Gates, his public-private partnership organizations like the Coalition for Epidemic Preparedness Innovations (CEPI) and public-sector bureaucrats, such as Dr. Anthony Fauci and Rick Bright, Ph.D., of BARDA and the Rockefeller Foundation, who have been working for years to create a new system that would speed up vaccine production.

During the COVID-19 pandemic period, even states that lacked legal structures to provide emergency authorization for new drugs created them, using the WHO’s Emergency Use Listing Procedure (EUL) as justification, and aided by the WHO’s COVAX vaccine distribution system. COVAX was co-led by the WHO, Gavi, CEPI and Unicef, which are all backed by Gates.

The goal now, Jones wrote, is to institutionalize the procedures that were put in place globally for COVID-19 to pave the way for a new pandemic market.

The One Health agenda, which requires “full-scale surveillance of the human-animal environment,” both before and during pandemics, is central to this plan, he wrote.

The four pillars of the emerging pandemic market

There are four pillars to the plan for securing this market. The pillars are embodied in the WHO’s recently passed IHR amendments and the proposed pandemic treaty.

1. Biosurveillance of “pathogens with pandemic potential”: The WHO is calling on member states to create infrastructure to conduct biosurveillance on entire populations.

WHO private stakeholders, like the Wellcome Trust and the Bill & Melinda Gates Foundation, have been funding such initiatives for years and continue to be at the forefront of similar initiatives today, Jones wrote.

2. Rapid sharing of data and research: Under the IHR amendments, the WHO’s director-general must provide support for member states’ research and development. In the pending treaty, that would include helping them rapidly share data during a pandemic.

Such sharing should help coordinate global pandemic responses and also “pandemic prevention.” That means building a globally coordinated effort to research and share data on diseases that don’t currently pose a public health threat but are allegedly “likely to cause epidemics in the future.”

The WHO’s announcement last week that it is facilitating data-sharing for a new mRNA bird flu vaccine from Argentina is one example.

Experts have raised concerns that incentivizing such “preventive R&D” could incentivize risky gain-of-function research, Jones wrote.

Jones also noted that it is “highly likely” that the same global organizations that partner with the WHO and are funded by its largest private donors will be the ones doing this research and development on vaccines for “future pathogens with pandemic potential” — and also the ones profiting from it.

3. New regulatory pathways: The WHO is developing new regulatory pathways for unapproved medical products to get to market during pandemic emergencies. The IHR amendments are vague on this, Jones wrote, but the proposed language of the treaty aims to speed up emergency authorizations of WHO-recommended investigational “relevant health products.”

The proposed treaty also seeks to compel member countries to take steps to ensure they have the “legal, administrative and financial frameworks in place to support emergency regulatory authorizations for the effective and timely approval of pandemic-related health products during a pandemic.”

4. Global mandates of unapproved products: The final key element in the Big Pharma-WHO plan to pave the way for a new pandemic market is shoring up the global capacity to mandate unapproved medical products.

According to Jones, in July 2023, the WHO adopted the European Union’s (EU) digital COVID-19 passport system, or the “immunity pass” which recorded people’s vaccination records, negative test results or records of previous infections.

“While a digital vaccine passport does not function as a hard mandate in which every citizen of a given population is forced to take a vaccine, it acts as a conditional mandate — one which offers the illusion of choice, but — in reality — restricts the civil liberties of those who do not comply,” Jones wrote.

The 2005 version of the IHR allowed for travel-based mandates that required proof of vaccination to enter countries when there was a public health risk. The new IHR, Jones wrote, expands on this by detailing the kinds of technology that can be used to check such information during future pandemics.

The WHO also is developing its Global Digital Health Certification Network, which expands the EU digital passport system to a global scale. It will digitize vaccination records and health records and will be “interoperable” with existing networks.

While interoperability makes it possible for decentralized data to be shared globally, Jones wrote, “The UN is seeking to impose digital identification as a ‘human right,’ or rather as a condition for accessing other human rights, for the entire global citizenry by 2030, as established in its Sustainable Development Goal 16.9.”

The initiative seeks to provide people with a “trusted, verifiable way” to prove who they are in the physical world and online.

Jones wrote:

“Verification systems of this size will place the right of citizens to do basic activities — like traveling, eating at a restaurant or working their job — in the hands of governments and potentially employers.

“The rights of civilians will be conditional, dictated by data stored in a massive digital hub that is global in its sharing abilities. Not only will domestic governments have access to the health information of their own citizens under this system, but an entire global bureaucracy will as well.”

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

August 7, 2024 Posted by | Civil Liberties, Science and Pseudo-Science, Timeless or most popular | , , , , , , | Leave a comment

Debunking the debunkers on the “myths” of antidepressants

By Maryanne Demasi, PhD | August 5, 2024

Recently, The Conversation ran an article which claimed to “debunk” a range of myths about antidepressants such as selective serotonin reuptake inhibitors (SSRIs).

Natalina Salmaso, a clinical psychologist at Carleton University in Canada, highlighted five common myths that make people hesitant to take antidepressants.

Salmaso said hesitancy is often “unfounded” and “may not be grounded in science” and that “debunking the myths surrounding antidepressants is critical to permitting educated treatment decisions for those who suffer.”

However, Salmaso’s article was full of omissions and falsehoods, so we decided to debunk the debunker.

Myth 1 – I am stronger if I do this without meds

Salmaso says that a person with depression is like an athlete with a broken leg.

An athlete cannot compete effectively with a broken leg, in the same way a person with depression cannot function effectively, because their brain “is no longer responding to everyday life.”

She adds that a person’s brain needs to “heal” before they can expect it to function like they did pre-depression and implied antidepressants can help.

This is grossly misguided. This feeds into the false narrative that depression is a brain disease that can be cured by antidepressants.

Antidepressants don’t cure people with depression and their symptomatic effects are so small that they lack clinical relevance.

Studies show that patients actually do better with psychotherapy, which has enduring effects. Further, psychotherapy halves the risk of suicide whereas antidepressants double this risk, in people of all ages.

Myth 2 – I will be dependent on antidepressants to be happy

Salmaso says that antidepressants won’t make people ‘happy’ per se, but they “allow people to experience all emotions in an appropriate and balanced way.”

However, this is not what patients report. SSRIs tend to make people feel “numb” and unable to experience emotions. Some describe it as an inability to feel love, attachment or sexual excitement.

Some experience sexual dysfunction, which can continue long after the drug is discontinued.

Salmaso says that antidepressants “are a long-term (typically at a minimum for a year) and (hopefully) curative treatment, much like chemotherapy for certain types of cancer.”

This is also misguided. Most people become depressed because they have stressful or depressing circumstances, which no drug can cure.

People have been misled to believe that antidepressants can “correct” a chemical imbalance in the brain. A systematic review in 2022 thoroughly debunked the hypothesis that depression is caused a serotonin imbalance.

Salmaso even says that “most studies show that if you take antidepressant medications for a year before coming off of them, the majority of people will not relapse.”

This is also incorrect. The majority of studies on relapse are flawed because they involve subjects already on antidepressants and when they suddenly stop them for the trial they experience withdrawals, which interferes with the assessment of relapse.

Also, the longer someone takes an antidepressant, the higher the probability of that person experiencing withdrawal effects.

Myth 3 – Meds will change who I am, I will be different or feel high

Salmaso says that antidepressants won’t change you, but rather “allow you to view things from a more balanced perspective.”

However, Danish psychiatrists have reported that half of the patients on antidepressants agreed that the treatment could alter their personality and that they had less control over their thoughts and feelings.

Far from rebalancing the brain, antidepressants alter the normal functioning of the brain and disrupt biological processes with potentially devastating consequences.

As far as “changing who you are,” there have been ample reports of out-of-body experiences (including akathisia) where people became suicidal or homicidal on antidepressants, even in people with no history of this behaviour.

A systematic review found that taking antidepressants increased aggression three times more than taking a placebo, in children and adolescents.

Myth 4: I will become addicted

Salmaso says that antidepressants “are generally not addictive and have a low potential for misuse.”

This is not correct. Antidepressants can lead to dependency. Many people experience withdrawal symptoms, which are very similar to those that people experience when they try to come off benzodiazepines.

Salmaso claims that some patients get headaches and other withdrawal symptoms when the stop taking antidepressants “suddenly” but says they are “generally short-lived and can be minimised by tapering off treatment slowly.”

However, it is well-documented that about half of patients on antidepressants cannot stop them without experiencing withdrawals symptoms, which for some, can persist for many years. These symptoms are very difficult to “minimise” even with slow tapering.

Myth 5: Meds should only be used as a last resort

Salmaso disagrees that antidepressants should be used as a last resort.

She says that reserving antidepressants only for extreme cases “doesn’t make sense” because depression can reduce “work productivity and has immense societal consequences.”

“The financial repercussions that can be attributed to depression in terms of the number of workdays missed, jobs lost, accidents caused, etc. are enormous,” she added.

However, studies examining the efficacy of antidepressants have not shown any meaningful effects, such as improvements in quality of life, and they make it more difficult for people to function.

In all countries where this relationship has been examined, the increased use of antidepressants has been accompanied by an increase in disability pensions for mental health reasons.

Salmaso argues that, “Depression significantly increases risk of cardiovascular disease, gastrointestinal disease, respiratory disease and Parkinson’s disease, to name a few. It also seems to worsen the outcomes for cancer.”

Antidepressants do not improve these conditions either. Overall, it is our view that Salmaso’s evidence and arguments are flawed and misguided.

August 7, 2024 Posted by | Deception, Fake News, Mainstream Media, Warmongering, Science and Pseudo-Science, Timeless or most popular | Leave a comment

UK High Court upholds Tory emergency order protecting minors from puberty blockers

By Susan Berry, Ph.D. | CatholicVote | July 29, 2024

A High Court judge in the United Kingdom (UK) ruled Monday that the previous conservative British government’s emergency order safeguarding children and teens from experimental puberty blockers is lawful.

The LGBT activist group TransActual and an unnamed young person brought a challenge to the Tory order issued in May in the wake of the release of a report detailing a comprehensive independent review led by British pediatrician Dr. Hilary Cass.

Cass and her team conducted a systematic examination of studies and guidelines related to the use of puberty blockers and other procedures associated with so-called “gender-affirming care” for children suffering with gender dysphoria.

They concluded the so-called “gender-affirming care” model of medical intervention for young people is based on “remarkably weak evidence.”

“The reality is that we have no good evidence on the long-term outcomes of interventions to manage gender-related distress,” Cass wrote, observing that puberty blockers were found in “multiple studies” to compromise bone density and fertility and lead to other harmful effects. The majority of minors who receive prescriptions for puberty blockers move on to cross-sex hormones, the study also found.

Justice Beverly Lang noted in her decision that she is “satisfied that the decision to make the emergency Order on 29 May 2024, was a rational one”:

Parliament has entrusted the Ministers to exercise the powers in section 62 MA 1968, in the exercise of their discretionary judgment. This decision required a complex and multi-factored predictive assessment, involving the application of clinical judgment and the weighing of competing risks and dangers, with which the Court should be slow to interfere.

Lang also observed, “There was cross-party support for this approach as the then Shadow Secretary of State for Health and Social Care (Mr Wes Streeting) said in response to the Statement: ‘I also welcome what she said about the justifiably cautious and responsible approach she is taking in relation to puberty blockers in the light of the Cass report.’”

The Labour Party’s Streeting said he planned to safeguard children against the controversial drugs “via any means, subject to the outcome of a legal hearing.”

Dr. Jane Orient, executive director of the Association of American Physicians and Surgeons (AAPS), told CatholicVote the High Court’s decision is “very encouraging news.”

“Governments have the right and responsibility to protect citizens from danger and from crime,” Orient observed, adding:

Giving minors drugs that will interfere with their normal development and likely sterilize them is criminal. It is not possible for minors to give informed consent, even if a judge or counselor asserts that they are “mature.” Puberty blockers keep them from becoming mature, and it is deceptive to claim that the effects are reversible. The drugs have a long list of very severe adverse effects, including osteoporosis with frequent fractures.

In a statement reflecting TransActual’s reaction to the High Court’s ruling, the group said it “condemns” the decision and will decide whether to appeal it.

Chay Brown, TransActual’s director for healthcare, called the ruling “disappointing,” noting that it “leans heavily” on what the group calls “the widely discredited Cass review”:

We are seriously concerned about the safety and welfare of young trans people in the UK. Over the last few years, they have come to view the UK medical establishment as paying lip service to their needs; and all too happy to weaponise their very existence in pursuit of a now discredited culture war. It is essential that NHS England and the Department of Health and Social Care now take urgent steps to reverse this perception.

In its statement, the group cited a white paper published in July by Professor Anne Alstott of Yale Law School and Dr. Meredithe McNamara, assistant professor of pediatrics at Yale School of Medicine – both co-founders of Yale’s activist Integrity Project, which tracks and attempts to “correct” and “oppose” efforts to protect children from life-altering transgender medical activists throughout America.

According to the Integrity Project:

Underserved and marginalized people are harmed most by the absence of sound science in law. U.S. states recently have adopted a number of measures based on scientific misinformation, in reproductive health, gender-affirming care and HIV prevention. The Integrity Project acts quickly to correct the scientific record and oppose these harmful measures.

The white paper that attempted to discredit the Cass report is co-authored by other transgender activist medical professionals such as Johanna Olson-Kennedy, M.D., professor of clinical pediatrics at the Keck School of Medicine of the University of Southern California, and Jack Turban, M.D., assistant professor of psychiatry & behavioral sciences at the Philip R. Lee Institute for Health Policy Studies, University of California, San Francisco.

In a May 2018 paper, Olson-Kennedy recommended that girls as young as 13 with gender dysphoria be subjected to top surgeries (elective double mastectomies). Drawing that conclusion only from 136 “completed surveys” at her gender clinic, she and her colleagues determined:

Chest dysphoria was high among presurgical transmasculine youth, and surgical intervention positively affected both minors and young adults. Given these findings, professional guidelines and clinical practice should consider patients for chest surgery based on individual need rather than chronologic age.

Turban was found in January 2022 by the Daily Caller News Foundation (DCNF) to have authored a controversial study at Stanford University that concluded childhood hormone treatment was associated with “favorable mental health outcomes.”

The study was funded by the American Academy of Child & Adolescent Psychiatry (AACAP), which opposes restrictions on gender-affirming care for children. AACAP, in turn, is supported financially by pharmaceutical companies Arbor and Pfizer, both of which manufacture hormonal drugs used for gender transitions, DCNF reported.

“This study is particularly relevant now because many state legislatures are introducing bills that would outlaw this kind of care for transgender youth,” said Turban in the press release about his study. “We are adding to the evidence base that shows why gender-affirming care is beneficial from a mental health perspective.”

Orient underscored in her comments to CatholicVote that “one effect” of hormone drugs to treat gender dysphoria “is to make the recipients life-long patients for a very lucrative industry.”

“Puberty itself is probably the best treatment for ‘gender dysphoria,’” she added. “After experiencing normal puberty, the vast majority of teens will accept their biological sex and escape from the pipeline leading to harmful cross-sex hormones, mutilating surgery, and life-long psychiatric care.”

In the UK, James Esses, co-founder of Thoughtful Therapists and co-ordinator of Declaration for Biological Reality, posted to X that the High Court’s ruling was “seismic.”

“We must never allow children to be irreversibly harmed in the name of an ideology again,” he added.

August 7, 2024 Posted by | Science and Pseudo-Science | | Leave a comment

TOP VACCINOLOGISTS FAIL TO PRODUCE SCIENCE TO SUPPORT SAFETY

The HighWire with Del Bigtree | August 1, 2024

In a recent interview, one of the world’s leading vaccinologists and co-author of what is considered to be the ‘bible of vaccines’, Dr. Paul Offit admitted that studies comparing unvaccinated children to vaccinated children have not been done, claiming they are impossible to do. All the while, lead author of the aforementioned book, Dr. Stanley Plotkin, the ‘godfather of vaccines’, made a recent statement in a published paper revealing the truth about safety trials on vaccines in the US, painting a picture of vaccine safety that falls far short of the safety claims our health agencies make.

August 4, 2024 Posted by | Science and Pseudo-Science, Timeless or most popular, Video | | Leave a comment

Even when it came to children, German regime ignored own scientists to impose strict COVID vaccine, mask mandates

By Michael Nevradakis, Ph.D. | The Defender | July 31, 2024

Germany’s response to the COVID-19 pandemic was based on political objectives, and the government implemented countermeasures that often contradicted scientific evidence and the opinion of the government’s own scientists, according to documents leaked by a former employee of Germany’s public health agency, the Robert Koch Institute (RKI).

An unnamed whistleblower released the “RKI Files” to investigative journalist Aya Velázquez, who on July 23 published the unredacted files — totaling 3,865 pages — in their entirety on Substack.

The RKI is Germany’s equivalent to the Centers for Disease Control and Prevention in the U.S.

According to the German newspaper Schwäbische Zeitung, the RKI Files “contain explosive details” about “child vaccinations and ‘resistance from the population,’” and show “that the RKI took a much more differentiated view of Corona policy than those responsible for politics and most of the media led the population to believe.”

“A whistleblower, a former employee of the RKI, approached me and passed on the data set to me” for reasons of “conscience,” Velázquez wrote on Substack.

According to the files, German regulators sought to skip Phase 3 trials of the Pfizer-BioNTech COVID-19 vaccine and “go straight into broad application.”

Other revelations include evidence of policymakers targeting and “nudging” children, and knowledge by policymakers and scientists that the COVID-19 vaccines were ineffective and led to severe adverse events.

Despite this knowledge — and for political reasons — government officials pursued measures rewarding the vaccinated and punishing the unvaccinated.

The RKI Files also reveal that policymakers and scientists sought to publicly ignore evidence of a “flattening curve” early in the pandemic, and evidence that masks and mass testing would not be useful in preventing infection.

Although some have questioned the legitimacy of documents contained within the RKI Files, the Robert Koch Institute, in an announcement carried by German news program Tagesschau addressing the publication of unredacted documents, did not confirm or deny the legitimacy of the documents themselves or their contents:

“The Robert Koch Institute has criticized the publication of unredacted minutes of the RKI crisis team on the COVID pandemic. The RKI expressly condemns the unlawful publication of personal data and trade and business secrets of third parties in these data sets and, in particular, any infringement of third-party rights.”

Other German mainstream news media outlets, including the mass-circulation Bild and Zeit newspapers, also reported on the release of the files.

‘Clear evidence that the general public was deliberately deceived’

The RKI Files mirror findings from the United Kingdom’s “Lockdown Files” and admissions last month by Dr. Anthony Fauci during congressional testimony that widespread masking and social distancing measures were enacted despite a lack of scientific evidence.

Widespread “vaccination of children” and policies barring the unvaccinated from many public spaces — for which the RKI “provided supposedly scientific legitimacy” — weren’t based on “rational, scientific considerations” but on “political decisions,” Velázquez wrote.

Stefan Homburg, Ph.D., professor of public finance at the University of Hannover in Germany, was part of a team that worked with the whistleblower to release the unredacted RKI Files. He told The Defender the documents show decisions were made “exclusively by politicians” and that “RKI did not support these measures.”

“We have now clear evidence that the general public was deliberately deceived,” Dutch lawyer Meike Terhorst told The Defender. “Politicians made the decisions, not health authorities.”

Dr. Christof Plothe, a member of the World Council for Health steering committee, told The Defender the files “show that it was never science that initiated ineffective and harmful masking, traumatizing social distancing and lockdowns, or that introduced a novel gene therapy labeled a ‘vaccine’ … It was politicians that demanded the measures.”

Germany’s pandemic-era Federal Minister of Health Karl Lauterbach figures prominently in the documents. Plothe said Lauterbach has “never worked with patients and is a pure lobbyist of Pharma.”

In March 2023, Lauterbach admitted that COVID-19 vaccine adverse events are prevalent and victims are being ignored.

German toxicologist Helmut Sterz, previously a researcher for major pharmaceutical companies — including Pfizer — told The Defender the documents show that pandemic decisions “were made by those who are responsible for the creation of this ‘pandemic’” and that “Real experts ‘disappeared’ from the public debate.”

Germany enacted among the strictest set of COVID-19 restrictions in Europe, according to the Oxford University COVID-19 Government Response Tracker.

“The measures that the German people were subjected to, besides mask mandates and social distancing rules, [include] a ‘lockdown of the unvaccinated’ that banned people from [public places] … Compulsory vaccination was imposed on military members and all people working in the health sector,” Plothe said.

Documents reveal EU discussions to ‘skip the Phase 3 trials’ for Pfizer shot

Pfizer was in discussions with the European Medicines Agency (EMA) to “skip the Phase III trials” for the COVID-19 vaccine “and go straight into widespread use,” documents from an April 15, 2020, RKI meeting show.

“Normally, you plan 12-18 months from the start of Phase I. EMA and Pfizer are considering whether to skip Phase III trials and go straight into broad use. If the regulators decide that, then it can go faster than 12-18 months,” the document says.

Minutes from an April 27, 2020, RKI meeting state, “There will be several vaccines that have been developed and tested in a fast-track process. Relevant data will only be collected post-marketing.”

According to German medical magazine Aertzeblatt, RKI documents from January and February 2021, after the first COVID-19 vaccines were introduced and administered, reveal discussions questioning the effectiveness of the AstraZeneca COVID-19 vaccine, stating it was “less perfect” and its “Ecology needs to be discussed.”

A Jan. 29, 2021 document (page 135), for instance, states that “STIKO [RKI’s Standing Committee on Vaccination] recommends vaccine only for <65-year-olds, as there is a lack of evidence for >65-year-olds, very wide confidence intervals, too uncertain, as two highly effective RNA vaccines are available.”

According to German magazine Tichys Einblick, the documents show that as early as the beginning of 2021,” the RKI knew about serious side effects of vaccinations, for example from AstraZeneca. Nevertheless, shortly afterwards, practically all important top politicians were publicly vaccinated with precisely this shot.”

These admissions came despite public rhetoric at the time stating that the shots would protect against both the spread of and infection from COVID-19.

Problems post-vaccination soon began to pop up in the RKI documents. A Feb. 8, 2021, document references a political furor in Germany after 14 fully vaccinated residents of a nursing home tested positive for COVID-19. The same document admitted that vaccination does not prevent less severe cases of the virus.

RKI documents from March 12 and March 15, 2021, referenced the identification of severe adverse events following AstraZeneca COVID-19 vaccination in Denmark, the Netherlands and Austria, and an April 9, 2021, document discusses a high rate of thrombosis cases tied to the AstraZeneca vaccine, particularly in males.

In turn, an April 23, 2021, document references six cases of cerebral thrombosis connected to the Johnson & Johnson (Janssen) COVID-19 vaccine in the U.S. but does not propose changes to Germany’s vaccination recommendations.

“It is particularly bad that the RKI recognized many vaccine injuries caused by AstraZeneca, but did not warn the public,” Homburg said. “The constant political pressure is also remarkable.”

‘It must be cool to get vaccinated’

The RKI Files also revealed efforts on the part of the German government and the country’s public health authorities to specifically target children with COVID-19 restrictions — efforts that were marked by political interference:

  • A May 19, 2021, RKI document states, “Even if STIKO does not recommend vaccination for children, [then-Health Minister Jens] Spahn is still planning a child vaccination program.”
  • A May 21, 2021, document states that while pediatric associations “are reluctant to vaccinate children … Politicians are already preparing vaccination campaigns to vaccinate the relevant age groups.”
  • A July 14, 2021, RKI document reveals discussions of an “influencer vaccination challenge on YouTube” and “developing material for younger target groups,” which would “be approached with more humor” — even vaccine reactions and side effects. “It must be cool to get vaccinated,” the document stated.
  • The minutes of a Dec. 15, 2021, RKI meeting reveal that Germany’s health ministry was “considering booster vaccination of children, although there is no recommendation and in some cases no approval for this.”

Such measures were promoted despite early knowledge that children were not significantly affected by COVID-19. A Feb. 26, 2020, RKI document referred to data from China finding that 2% of cases were in children, while a Nov. 30, 2020, document suggested that school settings were unlikely to contribute to the spread of the virus significantly, but that school closures would “exacerbate” the situation.

And a Dec. 4, 2020, RKI meeting examining data from several countries concluded that school reopenings did not lead to significantly greater spread of the virus.

‘The vaccinated must receive privileges of some kind’

Despite such findings, there was political pressure to reward the vaccinated and punish the unvaccinated, according to the RKI Files.

A Nov. 5, 2021, document said that media rhetoric regarding “a pandemic of the unvaccinated” was “not correct from a scientific point of view,” because “the entire population is contributing” to new waves of infection.

Yet, authorities decided to continue blaming the unvaccinated for the spread of COVID-19, because it would serve “as an appeal to all those who have not been vaccinated to get vaccinated,” according to the document.

The document also noted that Spahn “talks of the [pandemic of the unvaccinated] at every press conference … so it can’t be corrected.” The document contains an acknowledgment, though, that “one should be very careful with the statement that vaccinations protect against any (even asymptomatic) infection” because “as the time between vaccinations increases,” infection becomes more likely.

A May 10, 2021, RKI document contained a determination that telling the truth to the public would “cause great confusion,” while maintaining existing vaccination recommendations would serve “to save [the] vaccine.”

Instead, a Jan. 7, 2022, document stated that “the vaccinated must receive privileges of some kind,” including fewer travel restrictions, and that this was an objective that the German Health Ministry desired, while calling for further “testing of the unvaccinated after entry” into the country.

Similarly, a March 10, 2021, document suggested that COVID-19 vaccination should be promoted to the public as a means “to be able to participate in social life again,” for people who were tired of “bans and restrictions.”

Yet, a Dec. 4, 2020, RKI document suggested that the vaccinated should continue to comply with “hygiene measures,” while a Dec. 30, 2020, document suggested that the vaccinated should still wear masks, “as there is still a risk of transmission.”

German authorities wished to ‘avoid drawing attention’ to flattening curve

The RKI Files further reveal that, early in the COVID-19 pandemic, there was political pressure to maintain restrictions, despite the “flattening of the curve.”

A March 25, 2020, document admitted that “the curve is slowly leveling off,” but said, “We should avoid drawing attention to this in our external communications, to encourage compliance with measures.”

A Nov. 18, 2020, document contains an admission that respiratory illnesses were “well below” the previous year’s level, with a downward trend. Similarly, a Nov. 30, 2020, document states that general respiratory illnesses were “well below previous years.” A Jan. 27, 2021, document stated that a “no-COVID” policy is not feasible.

And according to a Feb. 25, 2022, document, RKI was prevented from downgrading its overall risk assessment of COVID-19 from “very high” to “high” even after the mostly mild symptoms of the Omicron wave were evident, due to intervention from Lauterbach and the German Health Ministry.

Use of masks by general public deemed ‘problematic’ — but imposed anyway 

The RKI Files also contain acknowledgments that masking and testing policies were ineffective in limiting the spread of COVID-19 but were pursued for political reasons:

  • A Jan. 27, 2020, document states that masking “does not make sense” for asymptomatic people, as there was no evidence that it would be a “useful preventive measure for the general population.”
  • An Oct. 23, 2020, document stated that FFP2 masks (similar to N95 masks) would be “misused” by the public and not offer protection, but instead might instill a false sense of security in people. “The harms of FFP2 masks may outweigh benefits,” the document states.
  • An Oct. 30, 2020, document says, “FFP2 masks have no added value if they are not fitted and used correctly” and are useless outside of “occupational health and safety.”
  • A Jan. 13, 2021, document states that FFP2 masks “can lead to health problems for people with preexisting conditions and should therefore remain an individual decision” and that “A general FFP2 mask requirement is not considered sensible.”
  • A Jan. 18, 2021, document found “No technical basis for recommending FFP2 masks for the population,” noting the risk of “undesirable side effects.”

Yet, by July 2, 2021, RKI documents contain suggestions, based on the American Academy of Pediatrics, for general mask wearing for children age 2 and older and that “The wearing of masks should be maintained … even at low incidences and should be understood as maintaining basic measures.”

RKI documents also questioned mass COVID-19 testing. A Feb. 3, 2020, document stated that positive PCR results after recovery “do not necessarily mean infectiousness,” while a July 29, 2020, document found that COVID-19 testing was ineffective, but a “political desire” for testing had to be “met.”

Similarly, a Dec. 16, 2020, RKI document suggested the suspension of elective procedures (planned operations), due to “pressure from the state governments.”

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

August 1, 2024 Posted by | Civil Liberties, Deception, Science and Pseudo-Science, Timeless or most popular | , , , | Leave a comment

Shocking testimony regarding Remdesivir

Health Advisory & Recovery Team | July 30, 2024

Some rather shocking testimony has emerged from the USA.

An American doctor working in Everett, Washington (just north of Seattle) called James Miller, recently published an attestation which can be downloaded from here.

This was written to be filed as evidence with some attorneys who are petitioning state Attorney Generals to investigate hospital administrations and others responsible for what some regard as homicides. More about that can be read here.

The whole statement is worth reading, but in our view the following in particular stands:

From just that small extract, the following can be surmised:

  • treatment was entirely protocol-driven — this person was well enough to be in a car and her “covid-19” was incidental; there were, however, recommendations in place that notwithstanding that, she should receive remdesivir just because a protocol said so
  • usually these protocols were followed, regardless of clinical need, but just because a person had a positive test
  • the protocols, however, could be flexibly applied and in this case a doctor decided that a valid criterion for making a decision was how “nice” the patient was
  • a treatment was actively avoided here “because she was nice” — indicating that the doctors knew that per-protocol they ought to be giving treatments which they themselves knew to be harmful

The core departure from medical norms on display here from which this fortunate patient escaped — the rigid application of “protocols” by compliant unquestioning doctors resulting in harmful treatment being given — is an extremely disturbing phenomenon. It would be naive to think this only happened in the USA, and was seen only in association with the particular treatment — remdesivir — mentioned here.

It’s worth noting that the tenacious Jessica Hockett has written this article in which she suggests a series of further questions she’d like to ask Dr Miller.

July 30, 2024 Posted by | Science and Pseudo-Science, War Crimes | , | Leave a comment

7 Reasons to Choose Lifestyle Interventions over Medications

Dr Philip Bosanquet | May 3, 2023

Why lifestyle changes (and lifestyle medicine) are often a better option than pharmaceuticals and conventional medicine when it comes to preventing, treating and managing chronic disease:

1. Effectiveness
2. Accommodating Complexity
3. Universal Relevance
4. User Experience
5. Cost Sustainability
6. Environmental Sustainability
7. Underlying Mindset

Lifestyle changes target the root cause of chronic disease. They help avoid environmental damage, pollution and chemical and plastic waste entering our ecosystems. Future generations are positively impacted by focusing on lifestyle factors.

Buy The Concise Nutrition and Lifestyle Guide: https://www.bosanquethealth.com/book-&#8230; (available worldwide via Amazon).

Visit Bosanquet Health: https://www.bosanquethealth.com

Dr Philip Bosanquet
The Low-Tech Lifestyle Medic

All content (including video and audio) copyright to Dr Philip Bosanquet 2023 ©

July 30, 2024 Posted by | Science and Pseudo-Science, Timeless or most popular, Video | Leave a comment

Does the new study on face masks show they prevent respiratory illnesses?

A new randomised trial in The BMJ is being touted as proof that surgical face masks are effective at an individual level for reducing respiratory infections

Maryanne Demasi, reports | July 28, 2024

Whether to wear a face mask to prevent respiratory illnesses has been one of the most divisive debates during the pandemic.

After a Cochrane review in 2023 found that face masks made “little or no difference” to the spread of respiratory viruses, the issue became highly politicised.

Tom Jefferson, lead author of the Cochrane review, told me “There is just no evidence that they make any difference. Full stop.”  The interview was picked up by media such as the New York Times and CNN, sparking an international furore.

New York Times columnist, Zeynep Tufekci pushed back in her own column arguing that despite no high-quality data, we could still conclude from less rigorous observational studies, that masks do in fact work.

Well-known science historian and co-author of Merchants of Doubt Naomi Oreskes agreed with Tufekci, claiming the public had been “misled” by the Cochrane review because it prioritised high-quality studies and excluded less rigorous ones.

When former CDC Director Rochelle Walensky was challenged about her controversial mask mandates in light of Cochrane’s findings, she lied to Congress claiming that the review had been “retracted” when it had not.

Then, in September 2023, former White House physician Anthony Fauci told CNN, “There’s no doubt that masks work.” Fauci said that while studies might show masks do not work at a population level, they do work “on an individual basis.”

Could this be true?

Well, a new study published in The BMJ is being touted as proof that face masks are effective at an individual level for reducing respiratory infections.

The study

Researchers in Norway performed a ‘pragmatic’ randomised trial in the off-peak period of “the normal influenza season” to determine if wearing a surgical face mask in public could reduce the risk of contracting a respiratory illness.

This study was sufficiently powered to detect a difference in outcomes in a real-world setting.

Over a 14-day period (between Feb-April 2023), 4647 participants were randomly assigned to either wear a surgical mask in public places (shopping centres, streets, public transport) or not to wear a surgical face mask in public places (control group).

The group wearing masks showed an absolute risk reduction of ~3 percent in “self-reported symptoms consistent with respiratory infection” (8.9% mask group; 12.2% control group, 95% CI 0.58 to 0.87; P=0.001).

The authors concluded, “Wearing a surgical face mask in public spaces over 14 days reduces the risk of self-reported symptoms consistent with a respiratory infection, compared with not wearing a surgical face mask.”

In an accompanying editorial, the authors of the study anticipated their findings would inflame an already divisive debate, and called for more “open and nuanced discussions” about face masks.

“We know exactly what to expect,” they wrote.

“Mask non-believers will describe the effect size as too small to be of interest, and they will intensively highlight any source of potential bias that might have inflated the results in the wrong direction. Of course, the mask believers will do the same but in the opposite direction.”

The authors said they would welcome “a nuanced debate around the potential biases and the interpretation” of the study findings, so here I go….

Analysis

I would argue that an absolute reduction of 3% in self-reported symptoms from people wearing masks is not a clinically meaningful result.

There are several reasons why.

First, in such a study, you obviously cannot blind the participants to one group or the other. People know they’re wearing a mask and may be less likely to report symptoms if they feel “protected.”

In fact, a pre-specified subgroup analysis showed a “beneficial effect was estimated for participants who reported that they believed face masks reduced the risk of infection,” indicating the study suffered from ‘reporting bias.’

Second, the study found wearing a mask changed people’s habits which may have accounted for the small difference between groups.

For example, people in the control group were more likely to attend cultural events than people wearing a mask (39% and 32%, respectively; P<0.001). Also, a larger percentage of people in the control group visited restaurants compared to those wearing a mask (65% and 53% respectively; P<0.001).

This is similar to the cluster-randomised trial of community-level masking carried out in Bangladesh. The study found a small effect of face masks which could be explained by changes in behaviour; 29% of people in villages wearing masks practiced physical distancing, compared to only 24% in the control (non-masking) villages. The apparent small effect of masks could therefore be due to physical distancing.

Third, masks were mandated across the world to reduce the burden of covid-19. But in this study, there was no difference in the number of self-reported or registered covid-19 infections between the control group and those wearing masks.

Fourth, the study showed people wearing a mask in public places sought healthcare for respiratory symptoms at a similar rate to people who weren’t wearing a mask, indicating that the mask was not reducing the burden on the healthcare system.

Fifth, with an intervention like surgical masks, compliance is always an issue because participants can feel uncomfortable or self-conscious wearing a face covering in public, and a small reduction in risk may not be worth it.

In this trial, only 25% of participants reported “always wearing a face mask” in public and 19% wore them less than 50% of the time. Had the trial been longer than 14-days, it’s likely that compliance would have diminished along with the small benefit.

The most reported adverse effect of wearing masks in public places was the unpleasant comments from other people.

This may also explain the difference in dropout rates. At follow-up, 21% of people assigned to wear masks did not respond to the questionnaire, compared to 13% in the control group, which again, suggests reporting bias.

Conclusion

What this study shows is that wearing a face mask in public during the flu season, might reduce the sniffles by a small percentage, but it won’t change whether you seek healthcare and might actually make you less inclined to go out and have fun.

This study does not show that community masking reduces the healthcare burden of disease associated with respiratory illnesses, which was the justification for mandating face masks during the pandemic.

I’d add that viruses are smaller than the pores in surgical or cloth masks (and masks are rarely worn properly), so it’s unlikely to be an effective public health intervention.

At the start of the pandemic before masking became political, Fauci had the right idea when he told 60 minutes, “Right now in the United States, people should not be walking around with masks.”

As shown in the 2023 Cochrane review, hand hygiene is likely to be more effective at reducing the burden of respiratory illnesses, and has no real downsides.

July 28, 2024 Posted by | Fake News, Mainstream Media, Warmongering, Science and Pseudo-Science, Timeless or most popular | | Leave a comment